SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs114622613 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47526446 | GAGTTTTTTCTATTC[A/G]TTGTAGACTATAAGA | 23607 |
rs114641458 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | CD2AP | GRCh38.p7 | 6:47499363 | ATACATACATGTATA[C/T]ATATATCTGTTTATT | 23607 |
rs114654393 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | CD2AP | GRCh38.p7 | 6:47608117 | GGTGTTCTTTAGGAC[G/T]AATTATTTTTTCTGC | 23607 |
rs114656925 | snp | A/C | 0.0391387 | 0.134304 | intron-variant | CD2AP | GRCh38.p7 | 6:47622095 | ATATGGCTGCCTATG[A/C]TGAATCATGCTGGTT | 23607 |
rs114677958 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | CD2AP | GRCh38.p7 | 6:47610408 | GAATATGGTACAAAA[A/G]TTATGGCCAAATAAA | 23607 |
rs114684558 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CD2AP | GRCh38.p7 | 6:47591942 | TGATTCTCTCACCTC[A/G]GCCTCCAGAGTAGCT | 23607 |
rs114714168 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CD2AP | GRCh38.p7 | 6:47618333 | AAAAAAAAACGAGTA[A/G]TCTTCCAAATTTGCA | 23607 |
rs114795313 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47530475 | ATATTTTGTGTCTGG[C/T]TTCTTTCAATCAGAA | 23607 |
rs114815916 | snp | A/C | 0.0232847 | 0.105357 | intron-variant | CD2AP | GRCh38.p7 | 6:47514416 | ACATTCTTAACTTCA[A/C]TGTTTTAGACTAAAG | 23607 |
rs114818512 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47602245 | TTTTAATGACATGAC[A/G]TAACTTTTTAGCTTC | 23607 |
rs114822361 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476588 | TCAACTTTTTTCTTT[C/T]ATCCTTTTTGGCTGC | 23607 |
rs114825391 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CD2AP | GRCh38.p7 | 6:47497201 | ATATTTTTCCTTTCC[C/T]CTTTTTGCTTTCCCC | 23607 |
rs114889123 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | CD2AP | GRCh38.p7 | 6:47533834 | CTAAATTAAGAAAAA[C/T]TAGTTCAGTCTTTTG | 23607 |
rs114889667 | snp | C/G | 0.0364509 | 0.129988 | intron-variant | CD2AP | GRCh38.p7 | 6:47577293 | CTCTTTTTGAGCTAA[C/G]TTTTATTGACTATAT | 23607 |
rs114928348 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47486670 | TCAGATGTGTACTTT[G/T]ACCTGAAATATTAAA | 23607 |
rs114971028 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | CD2AP | GRCh38.p7 | 6:47622201 | CCCACCGTGCCTCCC[C/G]CAACAGCCCTGTTTC | 23607 |
rs114986385 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | CD2AP | GRCh38.p7 | 6:47517056 | GCATGAATGATTTAG[C/T]GCCATGCCCTTGGTA | 23607 |
rs114991042 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47517616 | TTTAAAATAAATTAC[C/T]CAGCCTCAGATACTT | 23607 |
rs114996739 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | CD2AP | GRCh38.p7 | 6:47606850 | TTAGTTATTTTTAAG[C/T]GTACAATTAAATTAT | 23607 |
rs115030597 | snp | C/G | 0.0581099 | 0.160244 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521507 | CAGTGAGCCGAAATC[C/G]CACCAGTGCACTCCA | 23607 |
rs115035789 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | CD2AP | GRCh38.p7 | 6:47566621 | CTCCCTTCCCCCGCT[C/G]CTCACCCCTCAACAG | 23607 |
rs115038175 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CD2AP | GRCh38.p7 | 6:47593920 | CAGATTGTGTTTTAT[A/G]TATGTGTGTGTGTAT | 23607 |
rs115038661 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CD2AP | GRCh38.p7 | 6:47578360 | AGTTGCATCCCATTG[C/T]GCCTGATTAATTCTT | 23607 |
rs115044829 | snp | A/C | 0.0391387 | 0.134304 | intron-variant | CD2AP | GRCh38.p7 | 6:47512330 | CTGGGTTGCAGAACG[A/C]GACTCTGTCTCAAAA | 23607 |
rs115074734 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CD2AP | GRCh38.p7 | 6:47534874 | GTCACAGCTCACTGC[A/G]GCCTTGACCTCCCAG | 23607 |
rs115089905 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CD2AP | GRCh38.p7 | 6:47623050 | GACAATGAAAGCTAT[C/T]GTCTCAATCCAAATT | 23607 |
rs115098553 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | CD2AP | GRCh38.p7 | 6:47506899 | AATGAAGTTTGCTGC[A/T]TCAATTTGCTTATTT | 23607 |
rs115100602 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | CD2AP | GRCh38.p7 | 6:47538051 | CCACTGCTCCGGGCA[A/G]GAAAATTTTTTAAAA | 23607 |
rs115101948 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | CD2AP | GRCh38.p7 | 6:47600233 | GTAAGCTACAGACAC[A/G]TTAAATAAGCACTAT | 23607 |
rs115103997 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | CD2AP | GRCh38.p7 | 6:47492249 | GCTGGAAAGTCCAGC[A/C]TCTAGGCACTGGCAA | 23607 |
rs115105656 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47525361 | AGTATATTCCTTAGA[C/T]TTTAATTAGCTTAAG | 23607 |
rs115108864 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CD2AP | GRCh38.p7 | 6:47515151 | GTATTAGATAATTTA[C/T]GATAAAAAGATAATT | 23607 |
rs115179317 | snp | A/C | 0.0119091 | 0.0762411 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476569 | CTTGTTTAGGTGAGT[A/C]TATTCAACTTTTTTC | 23607 |
rs115286493 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | CD2AP | GRCh38.p7 | 6:47482191 | TTAGGAAATTTTTGT[G/T]TCAAAGTTGAATCAC | 23607 |
rs115291532 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | CD2AP | GRCh38.p7 | 6:47561306 | CCCTTAGTCCTAGGC[A/C]ATCATAGATCTGGTT | 23607 |
rs115295688 | snp | G/T | 0.0263992 | 0.111815 | intron-variant | CD2AP | GRCh38.p7 | 6:47614408 | ATTAGGCGTGTTCTA[G/T]CTCAGATAATAAGGA | 23607 |
rs115297785 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | CD2AP | GRCh38.p7 | 6:47484223 | ATAAAATTTTATTGG[C/G]ACTTCACTAACCTGA | 23607 |
rs115322088 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant | CD2AP | GRCh38.p7 | 6:47478626 | CTCGTGGGATGGGGG[A/T]GGGCGATCGAAAAAC | 23607 |
rs115350413 | snp | C/G | 0.0752113 | 0.178743 | intron-variant | CD2AP | GRCh38.p7 | 6:47614788 | TATCCCTGTAGTTCT[C/G]TCTTCTGTGCAGTTA | 23607 |
rs115352380 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | CD2AP | GRCh38.p7 | 6:47479059 | AATTTCTTTTGATAA[C/T]AAAGTTCGGTGTGGG | 23607 |
rs115461694 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47510228 | TGGTTTTGTATATAT[A/G]TGTGTCTGTGTTTAT | 23607 |
rs115495300 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | CD2AP | GRCh38.p7 | 6:47537851 | CATTGGCACAATCTC[A/G]GCTCACTGCAGCCTC | 23607 |
rs115530582 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CD2AP | GRCh38.p7 | 6:47606763 | AATGCATAATAATTA[C/T]ATCAGGGTAAATGCG | 23607 |
rs115557965 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | CD2AP | GRCh38.p7 | 6:47579763 | TCTATCCTAATAACA[C/T]AAATTAGTACTTTCC | 23607 |
rs115612698 | snp | A/T | 0.0437281 | 0.141251 | intron-variant | CD2AP | GRCh38.p7 | 6:47606496 | AGAAGGAAATTATCA[A/T]GAGGCTATAGCCACA | 23607 |
rs115621076 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47516328 | TTGAGGACAGAGCAA[C/G]AGAGCATAGAAAATC | 23607 |
rs115629636 | snp | A/G | 0.0752113 | 0.178743 | intron-variant | CD2AP | GRCh38.p7 | 6:47480524 | GACTACTTGAGGTCA[A/G]ATTCTCTTCTACCTA | 23607 |
rs115670904 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | CD2AP | GRCh38.p7 | 6:47600842 | GAAGAAAAGCAGATT[A/G]TTTGCCCAATTTTAA | 23607 |
rs115678806 | snp | A/G/T | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521754 | TAAGATAACTCTCAC[A/G/T]CCTGTAATCCCAGCA | 23607 |
rs115696894 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | CD2AP | GRCh38.p7 | 6:47581206 | CCAACTAGTTATTCT[A/G]CCGTTTCAAATGAAA | 23607 |
rs115699712 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497349 | TCCCTTCCCTTCCCT[C/T]CCCTTCCCCTTCCCC | 23607 |
rs115706515 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CD2AP | GRCh38.p7 | 6:47554915 | AGCAAATTATGATGG[A/G]GACCTAACTGAATTA | 23607 |
rs115707597 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | CD2AP | GRCh38.p7 | 6:47613770 | GGGATTGACTTCTCT[C/T]TAGTTATGGAAGTCC | 23607 |
rs115734663 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | CD2AP | GRCh38.p7 | 6:47598672 | AATCAAACATTGTAC[C/G]TTCTCCCTAATATGT | 23607 |
rs115794742 | snp | A/C | 0.0498117 | 0.149749 | intron-variant | CD2AP | GRCh38.p7 | 6:47539420 | GCAGCCTTTGGCAGA[A/C]CCACAGAAATAAGCA | 23607 |
rs115795085 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47601241 | GCTGTTATTTACTCC[C/T]TATATAGTAAACAGA | 23607 |
rs115799034 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47479095 | CATTAAACTAACTCC[C/T]TCAATCCTTTAAAAA | 23607 |
rs115810429 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CD2AP | GRCh38.p7 | 6:47524167 | CATTTTTTCCCTTTA[A/G]GAGTTAATACATTTT | 23607 |
rs115845543 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | CD2AP | GRCh38.p7 | 6:47543448 | TGCTAGGGCTACCAT[A/G]ACAAAATACCACAGA | 23607 |
rs115846655 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47494400 | GGTGGTAGCATGTGG[A/G]AAAGGGGAAATATAC | 23607 |
rs115864727 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | CD2AP | GRCh38.p7 | 6:47512640 | AGTATTTTACAAAGG[A/C]TATTGAACACAAGGA | 23607 |
rs115876136 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | CD2AP | GRCh38.p7 | 6:47577668 | ATCCTATAATAACTA[C/G]TATTATGGGAAAATT | 23607 |
rs115891611 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CD2AP | GRCh38.p7 | 6:47615709 | TCTGAGATTTGGTGG[A/G]GACACAGATGCAAAT | 23607 |
rs115907925 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | CD2AP | GRCh38.p7 | 6:47598190 | AATACAAATCAAAAC[C/T]GCAATGTGATACCAC | 23607 |
rs115912771 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | CD2AP | GRCh38.p7 | 6:47583446 | TTCCCTTCAACCCTT[A/G]TCAACCATTAATTTT | 23607 |
rs115917455 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CD2AP | GRCh38.p7 | 6:47525594 | GACATATTACAACAT[A/G]AAGGAGTGGTTTGTG | 23607 |
rs116038637 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CD2AP | GRCh38.p7 | 6:47617183 | TTGCCCAGGTTGATC[C/T]TGAACTCCTGGCCTC | 23607 |
rs116054772 | snp | A/G | 0.00993419 | 0.0697739 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476037 | ATTTAGTCTCTAGAA[A/G]CTTAAGGGCTCTGGG | 23607 |
rs116070424 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | CD2AP | GRCh38.p7 | 6:47612808 | AAAAAAAATTGAAAC[A/G]ATTGAACTCATAGAG | 23607 |
rs116094613 | snp | A/G | 0.0752113 | 0.178743 | intron-variant | CD2AP | GRCh38.p7 | 6:47479707 | TCTTAAATGGGATGC[A/G]GAATAAAATTAAACT | 23607 |
rs116159876 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47597844 | TCTGGAATAAAGTTG[G/T]CCTGGGTGATAATCC | 23607 |
rs116168708 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | CD2AP | GRCh38.p7 | 6:47480589 | CTTCAGTTTCTCAAT[C/G]TATAAATGGAATAAA | 23607 |
rs116187490 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CD2AP | GRCh38.p7 | 6:47493168 | TCATTTATTCCTTCT[A/G]TGCTTCTTCTTCATA | 23607 |
rs116202624 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | CD2AP | GRCh38.p7 | 6:47613856 | CCTGTAGCCAACTCC[C/T]GTCTTAGCTAGATCT | 23607 |
rs116203029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47492601 | TCCTCCCGCCTGGGA[C/T]TACAGGTGTGAGCTA | 23607 |
rs116219108 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | CD2AP | GRCh38.p7 | 6:47488412 | AATTTTCTAGTAGCT[A/G]CATTTAAAAAGGAAC | 23607 |
rs116279947 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | CD2AP | GRCh38.p7 | 6:47543582 | GGCTTGTAGAGGACC[A/G]CTGTCTCCTTGTTTT | 23607 |
rs116280299 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CD2AP | GRCh38.p7 | 6:47603522 | TAAAACAGGACTTTC[C/T]GGCTTAATGCATATT | 23607 |
rs116283345 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | CD2AP | GRCh38.p7 | 6:47502032 | GAAGATGGTGGCCAG[C/G]GTTGGGTTCACATTT | 23607 |
rs116292080 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | CD2AP | GRCh38.p7 | 6:47479039 | GTTTTGTTAAGTGGT[C/G]TAACAATTTCTTTTG | 23607 |
rs116315442 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47492452 | CAAACTCCTGGGTTC[A/G]AGTGATCCTCCCCCG | 23607 |
rs116330609 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CD2AP | GRCh38.p7 | 6:47613651 | TATCATAATTCTTAA[A/G]GGCCAAGGATTTTCA | 23607 |
rs116409287 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | CD2AP | GRCh38.p7 | 6:47602757 | AGCTGGGCATGATGG[C/T]GTGCACCTGTAGTCC | 23607 |
rs116411139 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | CD2AP | GRCh38.p7 | 6:47543353 | GGAATTAAAGATCAG[A/G]GTGACTGAATTATTG | 23607 |
rs116411631 | snp | C/G | 0.0748431 | 0.178382 | intron-variant | CD2AP | GRCh38.p7 | 6:47494182 | GTAGTTAAATCGTTA[C/G]TGTGAGGATTTATAT | 23607 |
rs116419913 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | CD2AP | GRCh38.p7 | 6:47567397 | ATATTTATTCATTCA[A/G]TATATTGAGTGCCTT | 23607 |
rs116446603 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | CD2AP | GRCh38.p7 | 6:47579948 | GAGAAAAAGTGAGGC[G/T]GAGTCATTCATCAGT | 23607 |
rs116506164 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | CD2AP | GRCh38.p7 | 6:47495918 | ACTCTCTTATACCAT[A/G]CAAGGATCTTGGAAC | 23607 |
rs116567946 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | CD2AP | GRCh38.p7 | 6:47479679 | CTAAAGTTAATTACA[C/T]AGTTCTTTTCTGTCT | 23607 |
rs116607853 | snp | A/G | 0.0232847 | 0.105357 | downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47627274 | AAAAATTCTAGACCC[A/G]TATGACTTTTACTGA | 23607 |
rs116611925 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CD2AP | GRCh38.p7 | 6:47618890 | TTTACCCTGTATTTG[C/T]AAAAGCACACCTAAG | 23607 |
rs116704498 | snp | G/T | 0.0325976 | 0.123435 | intron-variant | CD2AP | GRCh38.p7 | 6:47579020 | ATGGAATTTTAAAAT[G/T]GATATAGTTTTTAAA | 23607 |
rs116718247 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | CD2AP | GRCh38.p7 | 6:47575879 | TAAGGTTTAGTTCTG[A/G]GTTAAAATCTGGGCT | 23607 |
rs116733158 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47547913 | AAATTAAATAACTTA[A/C]TCCTGAATGATCATT | 23607 |
rs116754410 | snp | A/G | 0.00546417 | 0.0519829 | missense | CD2AP | GRCh38.p7 | 6:47624205 | AAATAGAGAAGCTGA[A/G]AAAAGCTGTCCTGTC | 23607 |
rs116755882 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | CD2AP | GRCh38.p7 | 6:47584988 | TCCCTAAAATCAGTC[A/G]GTTGTTCTTATAAAT | 23607 |
rs116791010 | snp | A/G | 0.0232847 | 0.105357 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521012 | ACTTGCTCAGTTCCT[A/G]TCCCTGGCTGGTCTG | 23607 |
rs116793840 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | CD2AP | GRCh38.p7 | 6:47525237 | ATTCTTATTTTCCTT[A/G]TTCTTTAGTAATACC | 23607 |
rs116861401 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47526510 | CTTTTGTCTTCAGAA[A/G]ATTTATTATATCTAA | 23607 |
rs117066215 | snp | A/T | 0.0966517 | 0.197444 | intron-variant | CD2AP | GRCh38.p7 | 6:47553499 | CTACAGGTGTGCACC[A/T]CCACACCTAGTGAAT | 23607 |
rs117196387 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47578952 | GTGAGCCACCGTACC[C/T]GGCCTCATTTTATCT | 23607 |
rs117252016 | snp | A/C/G | 0.00438476 | 0.0466401 | intron-variant | CD2AP | GRCh38.p7 | 6:47483384 | TGGTGGCTGGTAGCA[A/C/G]GCACTAGGTAGAGAT | 23607 |
rs117705268 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CD2AP | GRCh38.p7 | 6:47535077 | GCTGGAATTACAGAC[A/G]TGAGCCACCATGCTA | 23607 |
rs117827781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47584195 | AGTCTGACTTGTTTT[C/T]TTCACAGAGCAGAAG | 23607 |
rs118037815 | snp | A/G | 0.030278 | 0.119257 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520568 | AGGGAAGTCCCGGCT[A/G]TATACTGGGCCTTTT | 23607 |
rs118101228 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | CD2AP | GRCh38.p7 | 6:47550094 | AAATCTAAGACCTGA[A/G]ACTGTAACAGTTCTT | 23607 |
rs118161770 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | CD2AP | GRCh38.p7 | 6:47583107 | TTTTTTAAGGAGACT[G/T]TTTTTTAGAGCAGTT | 23607 |
rs137879436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47567746 | GAGATTTAATTCAGA[A/G]GCATTATAGAGTATA | 23607 |
rs137899013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47623291 | AAAGCATGTATTGTT[C/T]ATGTGCACTCTTGAG | 23607 |
rs137904732 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47527722 | GGAGTACGTTGAGTG[A/T]TACCTGCAGATTAGT | 23607 |
rs137906953 | in-del | -/G | 0.0232847 | 0.105357 | intron-variant | CD2AP | GRCh38.p7 | 6:47621770 | TCCTGATTTAATCTA[-/G]GAGGGTTGTATTTTT | 23607 |
rs137974940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47483328 | ATGTTTGGCAAAGTG[C/T]AGCGTGTACATGTAT | 23607 |
rs138004979 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | CD2AP | GRCh38.p7 | 6:47497457 | GGAGTGCAGTGGTGC[A/G]ATCTCTGCTCATTGC | 23607 |
rs138015074 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476440 | GCAAAATCTCTGAGG[A/G]TTAGCGCTGTACTTT | 23607 |
rs138027381 | snp | C/G | 1.6855e-05 | 0.00290297 | missense | CD2AP | GRCh38.p7 | 6:47624200 | GATGGAAATAGAGAA[C/G]CTGAAAAAAGCTGTC | 23607 |
rs138048256 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47588916 | GACCAATGAAACTTA[C/T]AAGAAGAATACTATT | 23607 |
rs138097263 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | CD2AP | GRCh38.p7 | 6:47491634 | TTTGGAATTTGTGTA[A/C]ATTGTTTATTTTTTT | 23607 |
rs138104337 | snp | A/C/T | 8.90931e-05 | 0.0066738 | intron-variant | CD2AP | GRCh38.p7 | 6:47533784 | TCCTTTCCTGCATAA[A/C/T]TACATCAAAATAGAA | 23607 |
rs138132845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47550208 | AACAGATAAATAGCT[A/G]TGACCTAATTAAACT | 23607 |
rs138163915 | snp | C/T | 6.59141e-05 | 0.00574045 | missense | CD2AP | GRCh38.p7 | 6:47574073 | TTTCAGAAACTGTTT[C/T]GGCTGGGCCTACTTC | 23607 |
rs138169326 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47550847 | TGCTGGAATACTACT[C/T]AGCCATAAAAAGGAA | 23607 |
rs138175469 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47589203 | TATTGGCTGAACTTT[C/T]ACTAAGAGTTTGTAT | 23607 |
rs138183632 | in-del | -/TGTGTGTG | 0.438666 | 0.164028 | intron-variant | CD2AP | GRCh38.p7 | 6:47491272 | ATATGTGTGTGTGTA[-/TGTGTGTG]TGTGTGTGTGTGTGT | 23607 |
rs138212393 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47492404 | GTTTCCCAGGCTGGA[C/G]TGCAAATGTGTGATT | 23607 |
rs138232533 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47604134 | ATGTGTTCCTAGCAA[C/T]GTGCAGATTGTAAGT | 23607 |
rs138330050 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | CD2AP | GRCh38.p7 | 6:47510062 | AATTTAATGAACTGC[C/T]TGCTAGCAGAGTATA | 23607 |
rs138376869 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47577978 | GATGTTATAGGATAC[A/G/T]TAGTAATAAAAAGGT | 23607 |
rs138428273 | snp | C/T | 0.000182115 | 0.00954066 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47533712 | CTATGGACTTCCAGC[C/T]GGAGGAATTCAGCCA | 23607 |
rs138469667 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47562208 | AAGGATGAATGCTTA[G/T]AAAGCAATATTATAA | 23607 |
rs138482652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47572363 | AAACATTACTGAAAT[A/G]CATATTTAAAACGGG | 23607 |
rs138507593 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | CD2AP | GRCh38.p7 | 6:47617982 | CAAGGCCCTGCTCAA[A/T]CAATTACCTTCATTA | 23607 |
rs138585531 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47484069 | TGTTGTTGCTTTTTA[A/C]ATTTTTTTTTGGTAA | 23607 |
rs138704346 | snp | A/G | 0.000106757 | 0.00730527 | intron-variant | CD2AP | GRCh38.p7 | 6:47533574 | AATATAACTTAACTT[A/G]CCTCTTTATTTATTT | 23607 |
rs138722443 | in-del | -/T | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626448 | GGGGTAAATCATGAA[-/T]TTTTTTTTCTACGTG | 23607 |
rs138726979 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47527941 | CATACCTGTAAATAT[A/G]TATTTGTGTCATATT | 23607 |
rs138727736 | snp | A/G | 0.010049 | 0.0701678 | missense | CD2AP | GRCh38.p7 | 6:47595872 | TTAGATGAAAAATCA[A/G]CACTGGAACAGAAAC | 23607 |
rs138729205 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CD2AP | GRCh38.p7 | 6:47588204 | TGACAGTATTTTCCT[C/T]ACCTACACTATTTAA | 23607 |
rs138739721 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47498845 | CAAATCATTTTTTTC[C/G]TGACTGATATCTTTC | 23607 |
rs138764627 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47498311 | CCAATGAGAAGTGTT[C/T]CAAGATGATTCTCAA | 23607 |
rs138780275 | snp | A/G | 1.64887e-05 | 0.00287125 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47609269 | CCAGATTATTGAATT[A/G]TTGTGCATTGTAGAA | 23607 |
rs138808988 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CD2AP | GRCh38.p7 | 6:47542164 | TTTATATTAAATATT[C/T]TACTCTCATTATGTA | 23607 |
rs138815625 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47514184 | CTATTAGCTGTAAAA[C/T]TTTCATTTTTAGTAT | 23607 |
rs138820199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47584119 | TTTTCCTTCAGTTTC[C/T]TTCTTTGTATATTTT | 23607 |
rs138828978 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CD2AP | GRCh38.p7 | 6:47596628 | AATGGTATTCTTTGT[A/G]TATATATGCCACATT | 23607 |
rs138857183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47579778 | TAAATTAGTACTTTC[C/T]TGGAAGAAATTGTAT | 23607 |
rs138956683 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47563532 | TATGGTCATGCATGC[A/G]TAAGTGCAGCAGGGT | 23607 |
rs139020301 | in-del | -/ATAA | 0.0391387 | 0.134304 | intron-variant | CD2AP | GRCh38.p7 | 6:47488173 | ACCTACTCCGTGTGT[-/ATAA]ATAAAGGGAAAGTTT | 23607 |
rs139028714 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47622927 | AGAAGTATTGCTGAT[G/T]ATGCATGCAGTAGTA | 23607 |
rs139056111 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | CD2AP | GRCh38.p7 | 6:47500776 | TTTTGAGACGGAGTC[C/T]TGCCCTGTCACCCAG | 23607 |
rs139060264 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47600320 | AAATCTTAATATTCT[A/G]ATTTTTCTAGCTTCA | 23607 |
rs139069886 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47561396 | TGAACTTCCTTACTC[C/T]GTGATATAAGATATT | 23607 |
rs139103350 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47516791 | CTGAGATTTTTAGTT[C/G/T]CAGAGTAATTGAGAT | 23607 |
rs139126337 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CD2AP | GRCh38.p7 | 6:47563998 | GATTGTATTGAAAGA[C/T]AGAAAAATCATTGAG | 23607 |
rs139216737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47558804 | TTTGTTGTGTCCGTG[C/T]CAAGTTTTGGTATCA | 23607 |
rs139232145 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47531191 | CTATGCCAGAGATTC[C/T]GAAACTTTCTTGGTT | 23607 |
rs139256944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47614763 | CAAAACGAAGTACAA[C/T]AAAAAGAGGTATCCC | 23607 |
rs139289085 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | CD2AP | GRCh38.p7 | 6:47604493 | TGTGTTTTTCTGTTT[C/G]TTTTTCTTTCTGCAA | 23607 |
rs139338761 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47536354 | CTATTAATATTAATT[A/T]AAAAAAACCCAAAAC | 23607 |
rs139383580 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CD2AP | GRCh38.p7 | 6:47590713 | ATGACTGTACAGTGG[A/G]AAGGTCTTATGTACA | 23607 |
rs139390657 | snp | C/T | 0.000307953 | 0.0124049 | missense | CD2AP | GRCh38.p7 | 6:47599384 | ATTCTGAACAGCTGC[C/T]CCTTAGACCAAAATC | 23607 |
rs139417092 | in-del | -/TGAA | 0.02016 | 0.0983543 | intron-variant | CD2AP | GRCh38.p7 | 6:47576823 | CAAACAGTAAATATT[-/TGAA]TGAATGGATTAATGA | 23607 |
rs139443996 | in-del | -/AGAA | 0.413083 | 0.189483 | intron-variant | CD2AP | GRCh38.p7 | 6:47485567 | TTTTGAAAGAAAATT[-/AGAA]AGAAAGAAATAAAAA | 23607 |
rs139506688 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47605777 | TACATGCTGATTTTC[C/T]GAGATCTTTTAATTT | 23607 |
rs139543379 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47624124 | TCTTAATGACATAGA[A/G]TAAAATAAACTACTA | 23607 |
rs139554230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47486492 | GAAGCATATGGAATA[C/T]TAGAATATAGATTCC | 23607 |
rs139650514 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497337 | TTTCCTTTCCTTTCC[C/T]TTCCCTTCCCTCCCC | 23607 |
rs139686373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47480503 | AAAGCATGGGCTCTG[A/G]ACAGAGACTACTTGA | 23607 |
rs139698309 | in-del | -/ATAAA | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47544152 | TAGTTATTAAAGAAG[-/ATAAA]ATAAATTTGAAATTT | 23607 |
rs139701860 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | CD2AP | GRCh38.p7 | 6:47529106 | TATTTTCTGACTCTT[A/T]CAGCGTTTCTCCCCT | 23607 |
rs139772521 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47505026 | CTTTTTTTTTTTTTT[A/T]TTTTTTTTTTAATTT | 23607 |
rs139789484 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47523402 | AGATGTTGTATACCT[G/T]AAGTATATGCAATTT | 23607 |
rs139814970 | in-del | -/ACAT/ACATATATAT/AT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47589565 | TACACACACACACAC[-/ACAT/ACATATATAT/AT]ATATATATATATATA | 23607 |
rs139820758 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CD2AP | GRCh38.p7 | 6:47569922 | CCCTTACTGGTAGTA[C/T]GTTGTGGATCTTTCT | 23607 |
rs139822478 | in-del | -/T/TTTCCTTTCA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497324 | TTTCCTTTCCTTTCC[-/T/TTTCCTTTCA]TTTCCTTTCCTTTCC | 23607 |
rs139826857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47510702 | AAAAATTCCAAGTGA[C/T]AATTCTAAATACTTA | 23607 |
rs139872181 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | CD2AP | GRCh38.p7 | 6:47487418 | CTTCTTGGCCAGGCG[C/T]GGTGGCTCACGCCTG | 23607 |
rs139912021 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | CD2AP | GRCh38.p7 | 6:47546012 | CCAAGAAGAAATCCC[G/T]GATTTACCTGAAAAA | 23607 |
rs139919991 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47503922 | CTGGGACAGTTGCCT[C/T]GCTGGTCTTCTCATT | 23607 |
rs139926926 | snp | G/T | 0.000115452 | 0.00759687 | missense | CD2AP | GRCh38.p7 | 6:47574182 | ATTTGGAGACATTTT[G/T]AAAGAAGGCTCTGTG | 23607 |
rs140011674 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47619562 | TTCGAATAATGACTT[C/T]TTTTCCTCTGGGTAG | 23607 |
rs140037275 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47535986 | TAAATTTTGCCTTTC[A/G]TAAGAACACTGGATG | 23607 |
rs140055368 | in-del | -/GAGA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47587140 | CTTGTTCCCATAGTT[-/GAGA]GAGGGAGCATTTTCA | 23607 |
rs140062848 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47583073 | CAGGTGTGAGCCTCC[A/G]TGCCTGGGCCAGTAT | 23607 |
rs140070953 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47499777 | AGACAGAGTCTTGCT[C/T]TGTCGCAGTGGCACG | 23607 |
rs140084714 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47589721 | CATTTGCCAATCTTG[A/T]AAGTGGTAGCTTAGC | 23607 |
rs140105501 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47585448 | AACAGTGGCTTTCAC[A/G]TATCGGACATCAGAC | 23607 |
rs140110267 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47557703 | TCTTTTTTGGTACCA[C/G]ACCATGCTGTTTTGG | 23607 |
rs140112241 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47494510 | AATTCCCATTCCTAG[C/G]TGGTATACAGCCCCT | 23607 |
rs140188898 | snp | A/T | 0.000975472 | 0.0220632 | missense | CD2AP | GRCh38.p7 | 6:47579473 | TCCAGATAAATGAAC[A/T]TGATAAAGACTTTCC | 23607 |
rs140250345 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CD2AP | GRCh38.p7 | 6:47591656 | CAGTAGGACATTGAC[C/T]CTCATCTGAATTAAT | 23607 |
rs140252241 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47490919 | TCTCTGTTGAAAAAC[A/G]TGTAAGAAATGCTGC | 23607 |
rs140317660 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47555087 | TTGGTCTGCTGAGTT[G/T]GCAAATGGCCTGTTT | 23607 |
rs140346011 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47506979 | ATAGTAGATCTTTCA[A/G]AATTGTAGTCAGTCG | 23607 |
rs140362194 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | CD2AP | GRCh38.p7 | 6:47549182 | ACTCCTCTTCAACAT[A/C]GTACTGGAAGTCCTA | 23607 |
rs140364003 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CD2AP | GRCh38.p7 | 6:47607239 | GATTCCAATTCTTGG[C/T]TGTATTCTTGTGAAT | 23607 |
rs140382320 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CD2AP | GRCh38.p7 | 6:47564896 | TATTGGAATGTCATA[C/T]CCACTATATTTGATT | 23607 |
rs140391156 | snp | C/T | 0.000263883 | 0.0114835 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47609302 | ACTGAAAAAGGATCA[C/T]GGGTAAGTAGCCCTT | 23607 |
rs140451111 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47603479 | CCAAGCCATCCTTTT[A/G]GAAACTGTCTTGGTG | 23607 |
rs140462829 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47602912 | CTCAAAAATAAACAA[A/C]AAAAAAGCAATTTTA | 23607 |
rs140480387 | in-del | -/GT | 0.168135 | 0.236216 | intron-variant | CD2AP | GRCh38.p7 | 6:47501666 | TTGTTGTGGTTGTTG[-/GT]GTGTGTGTGTGTGTG | 23607 |
rs140499628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47522783 | TTTTATTTAAAAATG[C/T]TTATTTTCAGTTTAT | 23607 |
rs140507123 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520563 | TGTGGAGGGAAGTCC[C/T]GGCTGTATACTGGGC | 23607 |
rs140527269 | snp | C/G/T | 0.00835141 | 0.0640778 | intron-variant | CD2AP | GRCh38.p7 | 6:47575010 | TGTTTTGGTTATTGA[C/G/T]ATACTATTAAGTTTC | 23607 |
rs140537787 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47517021 | TGGTGGGAGGTGATT[C/G]ACCCATGGGGGCTGA | 23607 |
rs140627775 | snp | C/T | 0.0179921 | 0.0931253 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47574218 | TCGGACAAGAACATC[C/T]AGTAGTGAAACAGAA | 23607 |
rs140659720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47533453 | GTGTTTTATTCTTCA[A/G]ATATGTTTGAGCAGA | 23607 |
rs140683024 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | CD2AP | GRCh38.p7 | 6:47621078 | AGGACTTCCAGTACT[A/G]TGTTGAAGAGGAGTG | 23607 |
rs140707650 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | CD2AP | GRCh38.p7 | 6:47527289 | GTTGCTGCTCTTGGT[A/C]TGTCTCCCTTCCCAC | 23607 |
rs140761836 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47582049 | GAAATATTTTTCTTT[A/G]AAGCCTGAAGAAAAG | 23607 |
rs140783842 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47589401 | ACACACACAAATGTA[C/T]ATACACACACATATA | 23607 |
rs140796042 | in-del | -/CAAA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47487702 | CTCAAAACAAACAAA[-/CAAA]CAAACAAACAAAACA | 23607 |
rs140800708 | snp | A/G | 0.000198124 | 0.00995103 | missense | CD2AP | GRCh38.p7 | 6:47609201 | CCATTAGAAATCAAA[A/G]CTAAAGTGGAAACAG | 23607 |
rs140814523 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47539335 | TGTCAAGCAGAGTAT[A/G]TTGAAGCTCTTCTTT | 23607 |
rs140821364 | in-del | -/TT | 0.0146672 | 0.084371 | intron-variant | CD2AP | GRCh38.p7 | 6:47517599 | CTGGCCCTAAACCTC[-/TT]TTTAAAATAAATTAC | 23607 |
rs140833424 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CD2AP | GRCh38.p7 | 6:47593339 | ATCTTATGAGATTTG[C/T]AAGTATCTGGAATAT | 23607 |
rs140890799 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47512296 | GCAGTGAGCCGAGAT[C/T]GCACCACTGCACTCC | 23607 |
rs140938422 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47511620 | CTACTTCCTTTGTAA[C/G]TCTTCTGTAAATCTT | 23607 |
rs140968071 | snp | C/T | | | missense | CD2AP | GRCh38.p7 | 6:47533708 | GCACCTATGGACTTC[C/T]AGCTGGAGGAATTCA | 23607 |
rs140982275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47571020 | TCCAAACCCCCTTCC[C/T]TGCCTTTTTTTTTGT | 23607 |
rs141029774 | snp | A/G | 0.00597247 | 0.0543191 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626582 | GAATTGTATTTCAGT[A/G]TTATTTTTTGTTTGT | 23607 |
rs141038904 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | CD2AP | GRCh38.p7 | 6:47599100 | TGTTATAATAATTTT[A/C]TACACTTAACTAAAC | 23607 |
rs141046819 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47500134 | AACCAGCATTCATCC[A/G]TAATAGCTGTACTAG | 23607 |
rs141050155 | snp | C/T | 1.65449e-05 | 0.00287614 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47576542 | TTAATCCTACAGTCA[C/T]TGGGACCCAAAACTC | 23607 |
rs141059861 | in-del | -/T | 0.0391387 | 0.134304 | intron-variant | CD2AP | GRCh38.p7 | 6:47513553 | TAGTGTTTTTTTTTC[-/T]CCCAGAATGCATGGT | 23607 |
rs141061103 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47497509 | AGCCATTCTCTCACT[C/G]AAGCCATCCTCTCAC | 23607 |
rs141061432 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CD2AP | GRCh38.p7 | 6:47560981 | TTTTGTCTTTCTCCG[A/G]TTTATGTATTTATCA | 23607 |
rs141074097 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47483268 | TTTAAGAAATCTGGA[G/T]GGAGGTCTATATGTG | 23607 |
rs141099364 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47556566 | GTTGGTCAAGCTGGT[C/T]TTGAACCCCCGACCT | 23607 |
rs141118107 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47553550 | TTTGTATTTTTAGTA[A/G]AGGTGGGATTTCACT | 23607 |
rs141166696 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47537770 | ATGGCCTAAGCATTA[C/T]GATTTTTTTATTGCT | 23607 |
rs141201012 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47573031 | AACTTTGTTTCTTAC[A/T]TAGATTATAAGGCTC | 23607 |
rs141213621 | snp | A/G | 1.65957e-05 | 0.00288055 | missense | CD2AP | GRCh38.p7 | 6:47533651 | GTTTGCCCATCAAAC[A/G]GGAAAGGCATGGGAA | 23607 |
rs141242954 | snp | A/G | 3.29886e-05 | 0.00406118 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47574188 | AGACATTTTTAAAGA[A/G]GGCTCTGTGAAACTT | 23607 |
rs141302240 | in-del | -/A | 0.158632 | 0.232706 | intron-variant | CD2AP | GRCh38.p7 | 6:47480733 | TTGTACCAACTTGGG[-/A]AAAAAAAAAATCTCA | 23607 |
rs141306036 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47588394 | GTATATAATACATAG[C/G]GAATACTTAATGCAG | 23607 |
rs141324748 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47479140 | AGAATAGCTTACAAA[A/G]AACAAAACACCCTGT | 23607 |
rs141325239 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47526269 | GTGTGTGTTTCTAGT[A/G]GTAAGGGATTGTAGC | 23607 |
rs141402367 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47576458 | TAACTGTAAATGGAA[A/G]CTTTGTTTAACAGTA | 23607 |
rs141435438 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47502743 | GTGATCTGCCTGCCT[G/T]GGCCTCCCAAAGTGC | 23607 |
rs141486275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47590003 | AAGAATGAAAGTAAA[C/T]CTTCATTGTCTAGAG | 23607 |
rs141487057 | in-del | -/TA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47491281 | GTGTATGTGTGTGTG[-/TA]TGTGTGTGTGTGTGT | 23607 |
rs141495068 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47623029 | ACTTTAATAACAGAT[A/C]GGGCTGACAATGAAA | 23607 |
rs141497013 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497246 | TCCTTTTCCTTTTCT[C/T]TTTTCCTTTCCTTCC | 23607 |
rs141540520 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47516139 | GGATAGTTTACATTG[A/T]GGTACCAACATCAAA | 23607 |
rs141544173 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47509039 | TCTAGCTTTTGATTT[A/G]AGTCAGAGATGTGTG | 23607 |
rs141565660 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47567198 | TCTAATTTTCTTTTA[A/G]GTATGCTTATAGAAC | 23607 |
rs141573811 | in-del | -/GGGGGGGG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47553193 | TAACACATATTGGCT[-/GGGGGGGG]GTTAGATGACTAACT | 23607 |
rs141672257 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47522717 | TTTCTAGCAATTTTT[C/T]TCTCTTCGTTTAGAA | 23607 |
rs141682474 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47623341 | TAAGGCAAGGCCTAT[A/G]TATTTCCTCATGCAG | 23607 |
rs141714272 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | CD2AP | GRCh38.p7 | 6:47616400 | CACCTGGCCTTAAAG[A/T]TGTTTTTAACAGAAG | 23607 |
rs141778404 | snp | A/T | 0.000429085 | 0.014641 | missense | CD2AP | GRCh38.p7 | 6:47577102 | TCCATTTGATAAGTA[A/T]GGTAAGGTGTTTCTG | 23607 |
rs141785030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47529385 | TCCAGTTTCCTCCCA[C/T]ATCCCCAAGATGCGT | 23607 |
rs141804989 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CD2AP | GRCh38.p7 | 6:47584565 | CATTTTTGATATCAT[C/T]TTCCACCCTTTTTGT | 23607 |
rs141820648 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | CD2AP | GRCh38.p7 | 6:47535062 | TTGGCTTCCCAAAGT[G/T]CTGGAATTACAGACG | 23607 |
rs141862005 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | CD2AP | GRCh38.p7 | 6:47556848 | TATACCCAGTAATAG[A/G]ATTGCTGGGTCAAAT | 23607 |
rs141878844 | in-del | -/TTTG | 0.40733 | 0.194287 | intron-variant | CD2AP | GRCh38.p7 | 6:47578042 | CACATAGTTACCTTT[-/TTTG]TTTTAGTGGCAATAG | 23607 |
rs141881558 | snp | A/C | 0.000560455 | 0.0167306 | missense | CD2AP | GRCh38.p7 | 6:47595933 | CCAAGAAACCTACTC[A/C]ACCTACCAAAGCCAG | 23607 |
rs141918071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47495599 | AAATAGATCTCGTCC[A/G]TGACTCTCTGGCTTT | 23607 |
rs141930421 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | CD2AP | GRCh38.p7 | 6:47550670 | ACTATCACTTGATCC[A/G]GCAATCCCACTACAA | 23607 |
rs141948109 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | CD2AP | GRCh38.p7 | 6:47598365 | TAAAGAACTAAAAGC[A/G]GATCTACCATTTGAT | 23607 |
rs141949321 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47563297 | TTACTTTAGGTAGGT[A/T]TAGAAAATGTTGGAG | 23607 |
rs141968689 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47543588 | TAGAGGACCACTGTC[A/T]CCTTGTTTTCTCACT | 23607 |
rs141987177 | in-del | -/C | 0.0232847 | 0.105357 | intron-variant | CD2AP | GRCh38.p7 | 6:47571859 | GGAGGTTGCTCTAAT[-/C]CTACCCTAAAAAAGC | 23607 |
rs142001609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47587382 | TCTTAAGTGATTCCC[C/T]GTTATTTCATGGGAT | 23607 |
rs142007124 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47617315 | TCCTTCACTGGTATC[C/T]TTGGCTTTTCTGTTT | 23607 |
rs142036472 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47505027 | TTTTTTTTTTTTTTT[A/T]TTTTTTTTTAATTTA | 23607 |
rs142044692 | snp | A/G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47500547 | ACTACTTCATGTAAC[A/G/T]AATCTGAAGGTATTA | 23607 |
rs142063376 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47558734 | TTTGCCAGTATTTTA[C/T]TGAGGATTTTCGCAT | 23607 |
rs142104493 | snp | A/G | 1.65663e-05 | 0.002878 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47533670 | AAGGCATGGGAATGT[A/G]GCAAGTCTTGTACAA | 23607 |
rs142176828 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47564811 | CAGTAAAATAATTAT[G/T]TTCCTCGTAGCTGTT | 23607 |
rs142313825 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CD2AP | GRCh38.p7 | 6:47572813 | CTCATGTGGGCTTAT[A/G]AAAATGAGATAATTC | 23607 |
rs142321602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47518370 | AGTTAGTGTTCTACT[A/G]CATTTGTGCCTTGCA | 23607 |
rs142338481 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47574847 | TTTAAAATAAAACCT[G/T]AAGCTGTTAATTTGG | 23607 |
rs142345554 | snp | C/T | 0.40733 | 0.194287 | intron-variant | CD2AP | GRCh38.p7 | 6:47616029 | ACCTTGTGATTCGCC[C/T]GCCTCAGCCTCCCAA | 23607 |
rs142364152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47568293 | ACTACCATGTTGGCT[A/G]TTCACTTTTGGAGAT | 23607 |
rs142381363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47513434 | GAGGTCCCAAACTGC[A/G]TAGGTTTTTGCATAA | 23607 |
rs142385278 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CD2AP | GRCh38.p7 | 6:47493816 | TCTCTTCAAGCTTAC[C/T]GATTCTTTCCTTGGC | 23607 |
rs142411264 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | CD2AP | GRCh38.p7 | 6:47609647 | AAGGCTGCAGTGAGC[C/T]GTGAACATGCCAGTG | 23607 |
rs142435486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47582343 | AATAACTATGCTTTT[A/G]TTATTTTTATAGTGT | 23607 |
rs142521665 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47604974 | ATGCCTTTTTTTCTG[A/C]CTTACCTTTGTGTCC | 23607 |
rs142569516 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47548484 | CCTGTAAAGATACAA[C/T]CCTCCTTGATTAAAT | 23607 |
rs142570426 | snp | A/G | 0.000115499 | 0.00759844 | missense | CD2AP | GRCh38.p7 | 6:47607976 | CAAAAGAAGAAGACA[A/G]TGCCAACCTGAAGCC | 23607 |
rs142628238 | snp | C/T | 8.40329e-05 | 0.00648147 | missense | CD2AP | GRCh38.p7 | 6:47533618 | AAATTAAAAGAGAGA[C/T]GGAATTCAAGGATGA | 23607 |
rs142643033 | snp | G/T | 0.000691859 | 0.0185863 | missense | CD2AP | GRCh38.p7 | 6:47574075 | TCAGAAACTGTTTTG[G/T]CTGGGCCTACTTCAC | 23607 |
rs142651164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47491826 | ACTGATTTTTTTTAA[A/G]AAAGTTATTAACAAC | 23607 |
rs142681200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47569035 | GAGATCATTAAGGAC[C/T]TAGACAAGAGCAGTT | 23607 |
rs142766907 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CD2AP | GRCh38.p7 | 6:47589229 | TGTATTAAGTGTTTA[A/G]TTGGAAGGTGCTATT | 23607 |
rs142790653 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | CD2AP | GRCh38.p7 | 6:47528356 | ATTTTTGTATTTTTA[G/T]TAGAGAGGTGGTTTT | 23607 |
rs142806324 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CD2AP | GRCh38.p7 | 6:47492592 | CTCAGGTTATCCTCC[C/T]GCCTGGGATTACAGG | 23607 |
rs142811741 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47584399 | TTTTTGTGAAAGTTG[C/T]AAGGTCATTGTCTAG | 23607 |
rs142811784 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CD2AP | GRCh38.p7 | 6:47522801 | ATTTTCAGTTTATTT[A/G]CAGATTTCCATAGTA | 23607 |
rs142849910 | snp | A/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625991 | AATAAATTAAATCTT[A/T]CTTTCTTTTAATGAC | 23607 |
rs142865262 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CD2AP | GRCh38.p7 | 6:47525767 | TTGTTGTACTACCTA[C/T]TCTTTATCTATAAGC | 23607 |
rs142890946 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47580034 | AGAGTTTTTAGAATA[C/G]AGGGAAAGAGCATCA | 23607 |
rs142905545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47544313 | CAGAAGTGTCTTTTA[C/T]TGTCGGTTTTTTTAG | 23607 |
rs142990861 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | CD2AP | GRCh38.p7 | 6:47586591 | TACCTAACAAAAATA[C/G]CTTTTGGGAATGGGT | 23607 |
rs143037743 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47515165 | ATGATAAAAAGATAA[G/T]TAGGCAGACTACTTT | 23607 |
rs143059600 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47527934 | TTTGGTTCATACCTG[C/T]AAATATATATTTGTG | 23607 |
rs143072918 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | CD2AP | GRCh38.p7 | 6:47489584 | TCATTTTCAGTTGAT[A/C]CTTAGTTACTAGCAT | 23607 |
rs143092614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47548923 | TCAGTAAATATGATA[C/T]GTCACATAAACAGAA | 23607 |
rs143200601 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47556601 | TGATCCACACGCCTC[A/G]GCCTCCCAAAGTGCT | 23607 |
rs143210943 | in-del | -/AA | 0.02016 | 0.0983543 | intron-variant | CD2AP | GRCh38.p7 | 6:47516201 | TACATCCTTTCATGC[-/AA]AGTTTGGTCCAGCTA | 23607 |
rs143213569 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47552666 | TCCTAAACCTAACTC[C/T]TCAGTTGTTGCCAGT | 23607 |
rs143244702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47561365 | TGTCATTTTGACATG[C/T]CTCCATTATTTTCTG | 23607 |
rs143250044 | in-del | -/G | 0.029116 | 0.117091 | intron-variant | CD2AP | GRCh38.p7 | 6:47537935 | TTTCTATTTTTAGTA[-/G]TGATGGGGTTTCACC | 23607 |
rs143260443 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47614021 | TGTTGGGCCTTCAAA[G/T]AATTGAAGAGAGTTA | 23607 |
rs143266548 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | CD2AP | GRCh38.p7 | 6:47511156 | TAATGGAGAAACTTC[A/G]CAAATACTGCCTTTA | 23607 |
rs143297472 | snp | A/G/T | 0.000347544 | 0.0131778 | missense | CD2AP | GRCh38.p7 | 6:47606235 | AAATAGACCAAAGAT[A/G/T]CCTGGAAGAAGGTTG | 23607 |
rs143304621 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CD2AP | GRCh38.p7 | 6:47604508 | CTTTTTCTTTCTGCA[A/G]GTTGCTTAAATATGC | 23607 |
rs143305290 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | CD2AP | GRCh38.p7 | 6:47506761 | GTCCAGCTTCGGCTC[C/T]GCATGAGAGGGAGAC | 23607 |
rs143350559 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47567003 | GTCACTCCCATTTTA[A/G]GGGTCAAGAAGTGGA | 23607 |
rs143363883 | in-del | -/G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497146 | TATGACCATGTCGTG[-/G/T]TTTTTTTTTTACTGT | 23607 |
rs143392059 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47482625 | CCTTGTAATCTGCCC[C/T]CCTCAGCCTTCCAAA | 23607 |
rs143401136 | in-del | -/GGT | 0.0532157 | 0.154195 | intron-variant | CD2AP | GRCh38.p7 | 6:47552182 | GGTGTTTGGGGAACA[-/GGT]GGTGTTTGGTTAGAT | 23607 |
rs143419962 | in-del | -/ACAT | 0.356811 | 0.226034 | intron-variant | CD2AP | GRCh38.p7 | 6:47619314 | CACATGTCCATGAGA[-/ACAT]ACAATGTTTGATTTT | 23607 |
rs143453079 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47522114 | TGATGAGTTTCATAT[A/G]AAAGGGTGCAGAGTC | 23607 |
rs143473459 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47578444 | TTGCAAACTCCTGGC[A/G]TCAGGCAATCTTCCC | 23607 |
rs143506275 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | CD2AP | GRCh38.p7 | 6:47483352 | CATGTATGTGGAACA[C/G]GCCTTTGGGAGTGGT | 23607 |
rs143521974 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47592595 | AGCATCTTTCAACCA[C/T]GTCTGAGTTTATATT | 23607 |
rs143594307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47579073 | CTGCTAAAAGTAATA[C/T]GTGGGAAATATTTTC | 23607 |
rs143599617 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476736 | TCCAAGGTTACTACT[A/G]TGGGCCACTGTGCTC | 23607 |
rs143630674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47573927 | ATCTTGCTCTTCTGG[A/G]TATTTCAGTACTGAA | 23607 |
rs143665843 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47608664 | GACTTTCTATTTTTT[C/T]AGTGAAATAGTTAAG | 23607 |
rs143689477 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47536124 | TGCTGCAAGGACTAT[A/G]TTGGTTATTTAGTGT | 23607 |
rs143729743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47532573 | TCTGTTTTAAATGAA[A/G]TTTGTCTGTTTATGG | 23607 |
rs143744141 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47615792 | ATTTTAATTTAATTT[-/A]ATTTATTTATTTATT | 23607 |
rs143754703 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47616541 | TTGTAAATTATCAGA[C/T]TTTATTTTATCCTTG | 23607 |
rs143776593 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47514883 | ACGGTGAAACCCAGT[C/G]TCTACTAAAAGTACA | 23607 |
rs143814652 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | CD2AP | GRCh38.p7 | 6:47533379 | TTGAGCCTCTCTTTC[C/G]TTTATCTTCATCTCC | 23607 |
rs143860830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47612679 | GACTACTATTCAGTC[A/G]CAAAAAAAGAATGAG | 23607 |
rs143906760 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CD2AP | GRCh38.p7 | 6:47508608 | TGGAGTGCAATAGCA[C/T]GATTTTGGCTCACTG | 23607 |
rs143960701 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47503573 | TTTAAGAAAATAGAG[G/T]CCAGGTACCTCTATA | 23607 |
rs143998552 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | CD2AP | GRCh38.p7 | 6:47499885 | AGGCATATGCCACCA[C/T]GCCCGGCTAATTTTT | 23607 |
rs144019654 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47618833 | TTGGCCTCTCACTGA[C/G]TTGTATTACAAATAT | 23607 |
rs144024088 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47517003 | AATATGGGAGGTGGG[A/G]CCTGGTGGGAGGTGA | 23607 |
rs144041826 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47564058 | AACTAGATGTACTTT[A/C]ACTATTTTATGTTAC | 23607 |
rs144063838 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47610986 | ATTTTTTTTTTTTTT[-/T]GAATATAAAACATTT | 23607 |
rs144064183 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47558895 | ATAGTTTCAGAAGGA[A/G]TGGTACCAGCTCCTC | 23607 |
rs144074210 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47511128 | CAGGGAAAAATAGTA[A/G]CTTAGTAGCTTTTAA | 23607 |
rs144090150 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47558383 | GAGTGATGAGAGAGG[A/G]CATCCTTGTCTTGTG | 23607 |
rs144093446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47534282 | TCTGTCTTATGACCT[C/T]AGAAAGATCATTTAA | 23607 |
rs144109265 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47614772 | GTACAATAAAAAGAG[G/T]TATCCCTGTAGTTCT | 23607 |
rs144113571 | in-del | -/ATTT/TTT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47615792 | TTTTAATTTAATTTA[-/ATTT/TTT]ATTTATTTATTTATT | 23607 |
rs144128568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47607354 | AGATGGTAGCTCTAT[A/G]TTTAGTTTTTTGAGG | 23607 |
rs144228197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47591923 | TCAAACTCCTAGGCT[C/T]AGGTGATTCTCTCAC | 23607 |
rs144265461 | snp | A/G/T | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47492593 | TCAGGTTATCCTCCC[A/G/T]CCTGGGATTACAGGT | 23607 |
rs144270509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47486518 | ATTCCTGCACTGAAG[A/G]AAATGGGATTTATTC | 23607 |
rs144280591 | snp | C/G | 0.0391387 | 0.134304 | intron-variant | CD2AP | GRCh38.p7 | 6:47585193 | CTGTAGTCCCAGCTA[C/G]TCAGGAGGCTGAGGC | 23607 |
rs144311101 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47551387 | TATGTTTATACAAAC[G/T]TAGATTGTGTTTATA | 23607 |
rs144321765 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47555850 | TGCATTGACAGTTTC[A/T]AAGCATAATGTTTGC | 23607 |
rs144322822 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CD2AP | GRCh38.p7 | 6:47581567 | GAAGTTGGTGTTGAA[A/G]GCTTTTTATATAGCT | 23607 |
rs144331531 | in-del | -/A | 0.0391387 | 0.134304 | intron-variant | CD2AP | GRCh38.p7 | 6:47576467 | ATGGAAACTTTGTTT[-/A]ACAGTATTATCTTTA | 23607 |
rs144368780 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47482059 | CCACTGTACCTGGCC[C/T]GGATAAAATCTTGAT | 23607 |
rs144411571 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | CD2AP | GRCh38.p7 | 6:47558467 | TATGACTTTGTCATA[A/G]ATAGCTCTTATTATA | 23607 |
rs144511704 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47582799 | TTTTTTGTTTTGTTT[G/T]TTTTTTTTTGTCTCG | 23607 |
rs144517088 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CD2AP | GRCh38.p7 | 6:47517306 | TTTTTTTTTGGAGGC[A/G]GTTTCTTACTCTGTC | 23607 |
rs144535252 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | CD2AP | GRCh38.p7 | 6:47568884 | TGAGGAAGATTAACT[A/G]AAAAGAAGACCAAGA | 23607 |
rs144542576 | snp | C/T | 4.95168e-05 | 0.00497553 | missense | CD2AP | GRCh38.p7 | 6:47595918 | CTCCACAAGTCCCAC[C/T]CAAGAAACCTACTCC | 23607 |
rs144554172 | snp | A/G | 1.67854e-05 | 0.00289697 | intron-variant | CD2AP | GRCh38.p7 | 6:47574302 | ATTCTCTCATTAAGC[A/G]TTTTTTAAAATGTAA | 23607 |
rs144554432 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47512388 | TTTTGTAAATCTGTG[A/C]ATATGGAGTGTGGAT | 23607 |
rs144577231 | in-del | -/TCTA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47575335 | TGTGCCCCTTCTAAC[-/TCTA]AAGCTTAGGATTATA | 23607 |
rs144577420 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47584465 | AGTTGATCCAACACC[A/G]TTTGTTGAAAAGACT | 23607 |
rs144578375 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47484818 | TTCAGCGTCCAGATA[A/G]TTCCAAGGGAGTGAC | 23607 |
rs144590370 | snp | C/G | 1.64814e-05 | 0.00287061 | missense | CD2AP | GRCh38.p7 | 6:47595968 | TTACTGAGATCTTCT[C/G]GAACAGTGTACCCAA | 23607 |
rs144595088 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | CD2AP | GRCh38.p7 | 6:47572977 | ATTTTTCCTTACCCC[G/T]TACCCCCGGTCTTAA | 23607 |
rs144621044 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47518956 | TCCCTCCCTACACTC[C/T]GCCTCTTGGTGTTCC | 23607 |
rs144718866 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | CD2AP | GRCh38.p7 | 6:47581335 | ATTATGGTAGACCTA[A/G]AAGTGTCTTCAAGAG | 23607 |
rs144746733 | in-del | -/A | 0.0368353 | 0.130617 | intron-variant | CD2AP | GRCh38.p7 | 6:47536964 | ATGAAATCTCTTGGC[-/A]ACACGTGAGGCAATA | 23607 |
rs144757637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47499103 | TTTTTTTGATAACTT[C/T]CTTACTTTCTGGCAC | 23607 |
rs144834724 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47593445 | ATCTAAAGGAGATAT[A/G]TAAGTTTTGTTTTTT | 23607 |
rs144866214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47504908 | CTAACGATCATCTGA[A/G]CCTTCAGTGAGTCAC | 23607 |
rs144886557 | in-del | -/ACACACACACAC/ATACACACACAC/ATACACACACACACACACACAC/ATACACACACACACACACACACACAC | 0.269809 | 0.249214 | intron-variant | CD2AP | GRCh38.p7 | 6:47589379 | GGAACTCTTGAATAT[lengthTooLong]ACACACACACACACA | 23607 |
rs144896627 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47589417 | ATACACACACATATA[C/T]ATACACAAATATACA | 23607 |
rs144903299 | snp | A/G | 3.30923e-05 | 0.00406756 | missense | CD2AP | GRCh38.p7 | 6:47582056 | TTTTCTTTAAAGCCT[A/G]AAGAAAAGGGTGAGG | 23607 |
rs144912461 | snp | C/T | 0.000148961 | 0.00862892 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47576586 | AACAAAAACAGATAC[C/T]GAAGGTAAAATTAAA | 23607 |
rs144923034 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47546801 | CCAGGTAACCTATAA[A/T]GGACAGTCTATCAAA | 23607 |
rs144929508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47547832 | TCAAGCACTCTCTCA[C/T]ACCACAGCGAAATAA | 23607 |
rs144947518 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47600644 | CTCATTGAAATTTAT[G/T]CGGTATGTTTTATAT | 23607 |
rs144961289 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47537100 | TTGATACTGATAGAT[C/T]ACTAGTGTTTATACT | 23607 |
rs144963139 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47599636 | AATTTTTATGGTCCT[C/T]ACTGATCAGACTTTA | 23607 |
rs144969474 | snp | G/T | 0.0144026 | 0.0836294 | intron-variant | CD2AP | GRCh38.p7 | 6:47596062 | AATTAGCTTACTGAT[G/T]TACTCACCTTTGACC | 23607 |
rs145050270 | snp | C/G | 0.0263992 | 0.111815 | intron-variant | CD2AP | GRCh38.p7 | 6:47547064 | AGAAACACATCAAAA[C/G]AGAACCTCTTTGAAG | 23607 |
rs145095901 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CD2AP | GRCh38.p7 | 6:47608139 | TTTTTCTGCCAAGAA[A/G]TGAAATAATTGCTGC | 23607 |
rs145098223 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47507688 | CTGACCTCGTGATCT[G/T]CCCGCCTTGGCCTCA | 23607 |
rs145119237 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47526588 | ATGGTTCTAGATCTT[C/G]AGCAATGAATTCATA | 23607 |
rs145175554 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47574668 | GAAAATATTAAATTA[C/G]TTGATATTTTGGCAC | 23607 |
rs145186807 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CD2AP | GRCh38.p7 | 6:47577264 | CTTGGCACGTAATAA[A/G]TGCTCAGAACGTTCT | 23607 |
rs145211815 | in-del | -/AT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47547496 | AATTCTATATATATA[-/AT]TATGCACCTAACACT | 23607 |
rs145227776 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47623127 | TCATCATAATATTTA[C/T]AGAATCATATCAAGG | 23607 |
rs145311126 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625780 | AGAAAATAGAAATGC[C/T]AGTAAACAACATAAT | 23607 |
rs145334999 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CD2AP | GRCh38.p7 | 6:47482084 | CTTGATTCATACAGA[C/T]AAGTAGTTGCAAATG | 23607 |
rs145347609 | snp | C/T | 0.000118756 | 0.00770479 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47599430 | ACTTACAGTAAGGAC[C/T]TCCAAAGAAACAGGT | 23607 |
rs145392451 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CD2AP | GRCh38.p7 | 6:47536592 | TGGCTTTTTTGGGAT[A/G]GTAATGAAGCCGTGA | 23607 |
rs145416870 | in-del | -/AAAC | 0.369965 | 0.219337 | intron-variant | CD2AP | GRCh38.p7 | 6:47487691 | CGAGACTCTGTCTCA[-/AAAC]AAACAAACAAACAAA | 23607 |
rs145480431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47555384 | AGAGGTCTTGAATTT[A/G]CAAGTGGAAATGTAG | 23607 |
rs145499219 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47496445 | AGTTTAAAAGAGCAG[A/G]GAATTTAACCCTATT | 23607 |
rs145518596 | snp | C/T | 0.00158194 | 0.0280796 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47554672 | CTGGTGGAGTGGAAC[C/T]CTGAATAACAAGTTG | 23607 |
rs145519213 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47549260 | TAAAGAGGAAGTCAC[A/G]CTGTCACTGTTTGCT | 23607 |
rs145551659 | snp | A/G | 0.427879 | 0.175668 | intron-variant | CD2AP | GRCh38.p7 | 6:47557033 | TAACTGGCATGAGAT[A/G]GTAGCTCATCGTGAT | 23607 |
rs145564945 | in-del | -/ATG | 0.00835141 | 0.0640778 | intron-variant | CD2AP | GRCh38.p7 | 6:47581000 | TGATTTTTATCAAGT[-/ATG]ATGTCTGTAAACATT | 23607 |
rs145649247 | in-del | -/T | 0.0241835 | 0.10727 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625649 | ATGATCATGCTTCCA[-/T]TTTTTTTTAGTTTTA | 23607 |
rs145656867 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47494523 | AGGTGGTATACAGCC[C/G]CTGACAGTCTTTCCC | 23607 |
rs145695770 | snp | A/C | 0.0532157 | 0.154195 | intron-variant | CD2AP | GRCh38.p7 | 6:47553320 | GCTAAGTAAAATTTG[A/C]CAGTGAATAGTTTAC | 23607 |
rs145701631 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47524280 | GGCTTCTGGGATATC[C/T]CCTGCTCTAGCTCCT | 23607 |
rs145810650 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47576183 | TGGTTTCATGCAGTT[C/G]TCCTGCCTTGGCCTC | 23607 |
rs145813128 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47571768 | TTGAGTTCTTTCTCT[C/G]TAGATTTCAGAGATT | 23607 |
rs145829930 | snp | A/G | 0.0043991 | 0.0466926 | intron-variant | CD2AP | GRCh38.p7 | 6:47587560 | CTGTGTCCCAGAATG[A/G]TAATAATATTACCAC | 23607 |
rs145847416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47586349 | TTGAAGACATAGCAA[A/G]TAGAACCATTAAAAA | 23607 |
rs145860839 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47572246 | AAGCAGGGGCCGGGC[A/G]CAGTGACTCATGCCT | 23607 |
rs145895420 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47483535 | GGGTATTTGCAGGAA[C/T]AAAAGTGAGCTTAGT | 23607 |
rs145901963 | in-del | -/GGGGGGGGTTT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47506859 | GGGAGAGAGCGGCTG[-/GGGGGGGGTTT]TGGCAGTTTCTAAGA | 23607 |
rs145906622 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47583850 | TGCCAAACTTCTTCC[A/C]ATGTGGCTGAACCAT | 23607 |
rs145907431 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497353 | TTCCCTTCCCTCCCC[-/T]TTCCCCTTCCCCTTC | 23607 |
rs145935021 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47510664 | GGTTGAATAAATAAA[C/T]GGGAGAAAGGATAAA | 23607 |
rs145960350 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47568469 | TGAGTAGGCTGGGCG[C/T]GGTGGCTTATGCCTG | 23607 |
rs145982068 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | CD2AP | GRCh38.p7 | 6:47564550 | TCCTTCTTTGTTTAA[C/G]CCTTTTACAATAACT | 23607 |
rs146010044 | snp | A/T | 0.000955582 | 0.0218375 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47574158 | GCCAAAGAAAATTCG[A/T]GGAATTGGATTTGGA | 23607 |
rs146054713 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | CD2AP | GRCh38.p7 | 6:47535898 | ATAAGTTTCTTCTTA[A/G]GTAGAAGTTAGACAA | 23607 |
rs146083274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47589619 | GTAGGAGAGCTACAA[A/G]TAAAATGAAGAATCA | 23607 |
rs146094320 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47585432 | TGGACAAAATGTATG[A/G]AACAGTGGCTTTCAC | 23607 |
rs146129948 | snp | A/C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47596995 | AGAAGAATATAAACA[A/C/T]GTTGAAAGCTGGATA | 23607 |
rs146166806 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47515440 | ATATCTGTATGAATA[C/T]TTTGCATATTCACAT | 23607 |
rs146178141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47563720 | CTCTCTGTAAGTGCT[A/G]CATACTATACGTGCT | 23607 |
rs146204960 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | CD2AP | GRCh38.p7 | 6:47618224 | ACTAGAGAGGCTGGG[A/G]CATGAGAATCACTTG | 23607 |
rs146216081 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CD2AP | GRCh38.p7 | 6:47614699 | GTTGCTCAGCACAGG[A/G]TTACCACAAGCCTTT | 23607 |
rs146225673 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | CD2AP | GRCh38.p7 | 6:47511921 | CCCAGCACTTTGGGA[A/G]GCCGAGGTGGGCGGA | 23607 |
rs146281813 | in-del | -/TT | 0.0232847 | 0.105357 | intron-variant | CD2AP | GRCh38.p7 | 6:47498263 | CAATACTTCAGTGAC[-/TT]TTAATTTTTCTTTTT | 23607 |
rs146285632 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47589403 | ACACACAAATGTATA[C/T]ACACACACATATATA | 23607 |
rs146286331 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47542012 | ACTGTTTTCCTTGCT[C/T]TAGAATATCTGCCAC | 23607 |
rs146319198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47543606 | TTGTTTTCTCACTTG[A/G]TCTTTCCTTTGTATT | 23607 |
rs146345336 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | CD2AP | GRCh38.p7 | 6:47536346 | AACCAGTACTATTAA[G/T]ATTAATTTAAAAAAA | 23607 |
rs146384979 | in-del | -/C | 0.0189856 | 0.0955633 | intron-variant | CD2AP | GRCh38.p7 | 6:47574344 | AACTCTGTTAGATTT[-/C]CTTTTTTTCAGATCA | 23607 |
rs146402480 | in-del | -/GT | 0.0360663 | 0.129354 | intron-variant | CD2AP | GRCh38.p7 | 6:47564320 | AATTAAAGCATATGA[-/GT]GTGAAATGATCTTTG | 23607 |
rs146408038 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47567327 | TTTAAAAGTCAAAGC[C/T]GGCAAAGGGAAATTC | 23607 |
rs146444716 | snp | C/T | 0.0036177 | 0.0423764 | missense | CD2AP | GRCh38.p7 | 6:47609163 | CCAGTGCTTCTAAAG[C/T]AAATACAACTGCTTT | 23607 |
rs146466127 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47500940 | TTTTAGTAGAGATGG[A/G]GTTTCACCATGTTAG | 23607 |
rs146466676 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CD2AP | GRCh38.p7 | 6:47616154 | TGGAGTGCAATGGTG[C/T]GATCTTGGCTCACTG | 23607 |
rs146480848 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | CD2AP | GRCh38.p7 | 6:47559109 | TTTCTAGTTTATTTG[C/T]GTAGAGGTGTTTATA | 23607 |
rs146508614 | snp | A/C | 0.0298908 | 0.118541 | intron-variant | CD2AP | GRCh38.p7 | 6:47556261 | TGTGATGTTCCCCTC[A/C]CTGTGCCCATATGTT | 23607 |
rs146539285 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47582796 | TTTTTTTTTGTTTTG[-/T]TTTTTTTTTTTTGTC | 23607 |
rs146562594 | in-del | -/AA | 0.00835141 | 0.0640778 | intron-variant | CD2AP | GRCh38.p7 | 6:47479497 | GTAACTTTCATACTC[-/AA]AAAAGTGCTCTTGAG | 23607 |
rs146568147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47531333 | TTTTAACAATTTAAC[C/T]ATTTAAAAAATAATA | 23607 |
rs146580154 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47526074 | CTGGCTCTTTTGGTA[A/G]AAGTGAATGAAGGGC | 23607 |
rs146616172 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47508719 | CCAGCTAATTTTTGT[A/G]TTTGTAGTAGAGATA | 23607 |
rs146636017 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47609916 | GTATTTTGGATCTGG[C/T]TGTGTATCTATACAT | 23607 |
rs146723866 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47490409 | GCTATTCATATGGTA[-/T]TTTTTTTGATCTGCT | 23607 |
rs146725236 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47607013 | CTTTCTGTTCTCTAT[C/T]TCCATTAGTTCAGTT | 23607 |
rs146736092 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47601640 | TTAAATTAGACGATC[A/G]TATGTTCCTAGTATT | 23607 |
rs146745462 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47502230 | CTTGTGTCTTCAAAG[C/T]GAGCAAGGGAAAAAG | 23607 |
rs146768764 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47599976 | AATCTGTACTTCCTG[-/T]TTTTTTTTTAATACC | 23607 |
rs146772227 | in-del | -/TACTGAG | 0.0232847 | 0.105357 | intron-variant | CD2AP | GRCh38.p7 | 6:47486563 | TGACCAGTGATGATA[-/TACTGAG]TACTGGCAGTAGTTA | 23607 |
rs146794166 | in-del | -/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47609532 | AAAAAAAAAAAAAAA[-/G]AAAAGAAAAGAAAAG | 23607 |
rs146803825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47480862 | ATAACCTTACAGAAA[C/T]CACATAGATACTTTT | 23607 |
rs146839987 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47532816 | TTGCATTGATATATT[A/G]CATCAATTTTAAGGG | 23607 |
rs146858632 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47627141 | ATTTTATTGCCAGTC[A/G]TGTCAGTCTTTATTG | 23607 |
rs146865776 | snp | A/G | 4.99804e-05 | 0.00499877 | missense | CD2AP | GRCh38.p7 | 6:47533632 | ACGGAATTCAAGGAT[A/G]ACAGTTTGCCCATCA | 23607 |
rs146867264 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CD2AP | GRCh38.p7 | 6:47527097 | AACTGTTTTTCCAAA[A/G]TAAAAGACTCCCCCC | 23607 |
rs146916668 | in-del | -/A | 0.00835141 | 0.0640778 | intron-variant | CD2AP | GRCh38.p7 | 6:47496280 | CCACACATTTAAGAT[-/A]ACTAATCTGCTTCCT | 23607 |
rs146936690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47483299 | CCTACAGTCAGCTTG[C/T]CAGCATCAGGGATAT | 23607 |
rs146946338 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | CD2AP | GRCh38.p7 | 6:47538179 | GTAAAATGGCCGAAT[C/T]AGTGTTTCTCATAAC | 23607 |
rs146954928 | snp | C/T | 0.00835141 | 0.0640778 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476414 | TTCGTATCTCACCCC[C/T]CTAGAAGAATGCAAA | 23607 |
rs146965123 | snp | C/T | 1.73345e-05 | 0.00294397 | intron-variant | CD2AP | GRCh38.p7 | 6:47533768 | AGAGTATGTAAATAA[C/T]TCCTTTCCTGCATAA | 23607 |
rs146992362 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47505031 | TTTTTTTTTTTTTTT[A/T]TTTTTAATTTATTTT | 23607 |
rs146994430 | in-del | -/AGTAGCTT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47511132 | GAAAAATAGTAGCTT[-/AGTAGCTT]TTAATGGAGAAACTT | 23607 |
rs147051428 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | CD2AP | GRCh38.p7 | 6:47565905 | AAAAGCCAAAATCTT[C/T]TAAAATGGCTACAAA | 23607 |
rs147074347 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | CD2AP | GRCh38.p7 | 6:47561811 | ATTGAGACGGAGTCT[C/T]GCTCTGTCACACAGG | 23607 |
rs147090901 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47605500 | ATGTAGCTTTTTCTC[-/T]TTTTTTTTTTGGTAT | 23607 |
rs147168945 | in-del | -/ACACACACACAC | | | intron-variant | CD2AP | GRCh38.p7 | 6:47532377 | TATATATATATGTAT[-/ACACACACACAC]ACACACACACACACA | 23607 |
rs147188917 | snp | A/G | 9.89071e-05 | 0.00703163 | missense | CD2AP | GRCh38.p7 | 6:47579415 | GGCTGGTGGAGGGGC[A/G]AACTTAATGGTAAAG | 23607 |
rs147196518 | snp | G/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47477444 | GGCTGCTTCGCTGCA[G/T]AAAGTAACTCCGCGT | 23607 |
rs147211221 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47573964 | AATTTTTTTTCTACT[C/G]TGTTTTATTAGAAGG | 23607 |
rs147254896 | snp | C/G/T | 0.000197847 | 0.00994434 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47595940 | ACCTACTCCACCTAC[C/G/T]AAAGCCAGTAATTTA | 23607 |
rs147259877 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47589413 | GTATATACACACACA[C/T]ATATATACACAAATA | 23607 |
rs147295432 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | CD2AP | GRCh38.p7 | 6:47604485 | TCTTTTCCTGTGTTT[C/T]TCTGTTTCTTTTTCT | 23607 |
rs147298950 | in-del | -/GAACTCTAGTTCCATCCATGTTGCAAATG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47607098 | TTCACTTAACATAAT[lengthTooLong]GAACTCTAGTTCCAT | 23607 |
rs147303862 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47503611 | TCATTGTTGCTCTGT[G/T]TCCTGCTGGATAGTA | 23607 |
rs147312611 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | CD2AP | GRCh38.p7 | 6:47499889 | ATATGCCACCACGCC[C/T]GGCTAATTTTTGTAT | 23607 |
rs147319099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47598986 | TTAGCTCTCACTGTT[A/G]CTTACCTTCCAGAGT | 23607 |
rs147371535 | in-del | -/A | 0.0391387 | 0.134304 | intron-variant | CD2AP | GRCh38.p7 | 6:47586277 | AGTATCTGAAATGAG[-/A]AACACTGAATGGAAT | 23607 |
rs147409273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47528644 | GTGGAAATACAATAA[A/G]ACATAATCCCTTCTG | 23607 |
rs147418998 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47523170 | ACGACTTTAATAGAA[C/G]AATTCAAGAGCTAGC | 23607 |
rs147421544 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624919 | TTTAGAATATTTTAT[A/G]TTGCTTGCACTATAG | 23607 |
rs147506255 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | CD2AP | GRCh38.p7 | 6:47557593 | AGGGAATCCTTTCCC[C/T]ATTGCTGGTTTTTGT | 23607 |
rs147528894 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47552805 | CTTTAAGTCTGATAA[A/G]AATTCTGGTCACTTC | 23607 |
rs147537850 | snp | C/T | 1.6853e-05 | 0.0029028 | missense | CD2AP | GRCh38.p7 | 6:47599318 | TTAATGGGGAAGTTT[C/T]TAGCATTTCATCAAA | 23607 |
rs147537923 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47604600 | GTGGGTTGTTAATGC[A/G]CACATCAGTGTAAAA | 23607 |
rs147561637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47587163 | GAGCATTTTCAAATC[A/G]TGGCTAGGACCAATT | 23607 |
rs147643584 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47569395 | AGCTGAGGAAGATAT[A/T]TCTGACTTTTGATAT | 23607 |
rs147684729 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | CD2AP | GRCh38.p7 | 6:47571013 | CACTAAATCCAAACC[C/G]CCTTCCCTGCCTTTT | 23607 |
rs147733484 | in-del | -/T | 0.0240643 | 0.107019 | intron-variant | CD2AP | GRCh38.p7 | 6:47494000 | CCCTTAGCATATTAA[-/T]CATAGTTATTTTAAA | 23607 |
rs147747925 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47591170 | GCAAAATGAATCTTA[C/G]GATTTCGTTGACATA | 23607 |
rs147755450 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47495277 | AGGAGAGGGTGAGAT[G/T]TGAGATGGAGACGTA | 23607 |
rs147766136 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47537349 | GCTCTTTGACATTGA[A/T]GTATTCTGACTGGTA | 23607 |
rs147770125 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47600091 | CTGGTAATTGTTAAT[A/G]TTTTGTGTAGTGCTT | 23607 |
rs147789316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47591972 | TGGGACTAAAGGTAC[A/G]TGTCACCATAACTGG | 23607 |
rs147861711 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47517579 | GCAGGCCTAAGCCAC[C/T]GCGCCTGGCCCTAAA | 23607 |
rs147875817 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625930 | CTCTTCTGTTAAATA[C/G]AATAGGTTTAAATGA | 23607 |
rs147875832 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47565461 | AACCAGTGACTGTAT[A/G]TACTTGTCTTTTCCA | 23607 |
rs147885645 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47621415 | ATCATGGTGGATTAT[C/G]TTTTTGATATGTTGT | 23607 |
rs147894238 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497245 | TTCCTTTTCCTTTTC[C/T]TTTTTCCTTTCCTTC | 23607 |
rs147947745 | snp | A/T | 0.000153988 | 0.00877328 | missense | CD2AP | GRCh38.p7 | 6:47577061 | TACTAATGAAGATGA[A/T]CTTACTTTTAAAGAG | 23607 |
rs147959117 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47546994 | AGAATTCACTACTAC[A/G]AAGCCAGTACTGCAA | 23607 |
rs147960960 | in-del | -/T | 0.0232847 | 0.105357 | intron-variant | CD2AP | GRCh38.p7 | 6:47503981 | TGCATTTGGTCATAC[-/T]TTTTGTGTTTCAGCA | 23607 |
rs147989828 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47522250 | GCAGAGAAATATCAG[C/T]GGAATGATATCAAAA | 23607 |
rs148008333 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | CD2AP | GRCh38.p7 | 6:47539225 | CTTGATAAATGTTTA[C/T]AGTTATTCTGGTGTT | 23607 |
rs148013081 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47578947 | CAGGTGTGAGCCACC[A/G]TACCCGGCCTCATTT | 23607 |
rs148027415 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47589419 | ACACACACATATATA[C/T]ACACAAATATACACA | 23607 |
rs148066770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47584540 | CAGTAACTAACTGAC[C/T]CCCCGATTACATTTT | 23607 |
rs148086371 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | CD2AP | GRCh38.p7 | 6:47556829 | ATTTATAATCCTTTG[A/G]GTGTATACCCAGTAA | 23607 |
rs148096534 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47609563 | AAAAAGCCAGGCTTG[G/T]TGACACATCCCTGTG | 23607 |
rs148125704 | snp | C/T | 0.000153988 | 0.00877328 | missense | CD2AP | GRCh38.p7 | 6:47595932 | CCCAAGAAACCTACT[C/T]CACCTACCAAAGCCA | 23607 |
rs148147683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47616917 | TGGTTTAGATGATAC[C/T]ACATCCTATTGTCTC | 23607 |
rs148200489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47573013 | TCTGGATTTTTACTC[C/T]AGAACTTTGTTTCTT | 23607 |
rs148222040 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47490355 | CCCAAAAGTTTTCCT[A/G]GAGTTGTTTTTTGGT | 23607 |
rs148273065 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47553514 | ACCACACCTAGTGAA[-/T]TTTTTTTTTTTTTTT | 23607 |
rs148278636 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47534628 | GAGAATCACTTGAAC[A/T]CGGGAGGTGAGCCGA | 23607 |
rs148296902 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CD2AP | GRCh38.p7 | 6:47603450 | CTGATTTATTACTCT[A/G]GCCTCTTAAAGCACC | 23607 |
rs148298002 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47502557 | GGAGTGCAGTAGCAC[A/G]TTCTTGGCTCACTGC | 23607 |
rs148350783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47508827 | TGGGATTACAGGTGT[A/G]AGCCTGGCCTCACAC | 23607 |
rs148359908 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47567032 | GAAACTCCTGAGATT[A/T]TTTAACTACTGAGTG | 23607 |
rs148382020 | in-del | -/T | 0.0232847 | 0.105357 | intron-variant | CD2AP | GRCh38.p7 | 6:47600591 | TATATTTACTACTAA[-/T]TTCTGGGAATTGAAA | 23607 |
rs148389777 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CD2AP | GRCh38.p7 | 6:47604729 | ATATTTAAATTCAAC[C/T]GCCTTCAGATTATAT | 23607 |
rs148444148 | snp | A/G | 0.039522 | 0.134904 | intron-variant | CD2AP | GRCh38.p7 | 6:47512090 | GTGAAGCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 23607 |
rs148467802 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47568916 | AGCACAGAAGGAGAG[A/T]GCCAGAAAGAAACCT | 23607 |
rs148483242 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47485280 | ACAGCCCTATGCACG[G/T]TTTTCACCAGTGGGA | 23607 |
rs148520057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47524747 | CCTTCTCTGAATACA[A/G]GAGGAATAGTTTAAA | 23607 |
rs148540599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47543821 | ATTCAGTTCCTAGTA[A/G]GTAGATGTGGGGTGG | 23607 |
rs148600751 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | CD2AP | GRCh38.p7 | 6:47558608 | TCATTGATTCTGTTT[A/G]TGTGATGGATTATGT | 23607 |
rs148664732 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47561918 | CCCAAGTAGGCGCCC[A/C]CCACCACACCCAGCT | 23607 |
rs148672857 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CD2AP | GRCh38.p7 | 6:47479045 | TTAAGTGGTGTAACA[A/G]TTTCTTTTGATAACA | 23607 |
rs148677398 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47619303 | AGCTTAGCTCCCACA[C/T]GTCCATGAGAACATA | 23607 |
rs148729751 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47574743 | AACTTCTTTGAATGT[A/G]TGGAGTATTTTATTT | 23607 |
rs148749357 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47492855 | TGAGTGTTTTATATG[A/C]TTCCATTTTATGTCC | 23607 |
rs148759154 | snp | A/C/T | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47552072 | GTGTCAAGGTCACAA[A/C/T]TGTAGGATGAGAGAT | 23607 |
rs148844193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47591980 | AAGGTACATGTCACC[A/G]TAACTGGCTAATTTT | 23607 |
rs148855298 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47497096 | TTGCTGTACGATAAT[G/T]TGATTGTCAAAGTTA | 23607 |
rs148898525 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47502261 | TCTCCTATTAAGATG[A/G]GCATTACAGCCTTAA | 23607 |
rs148916380 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47507792 | GTTGAAATACTCCTT[C/G]ATCAATGGGCTGCAA | 23607 |
rs148922365 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | CD2AP | GRCh38.p7 | 6:47608451 | ACATGTGTTAGGTGT[C/T]TTGTCAAAATTTTTA | 23607 |
rs148969035 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47514745 | GAAAAAATGTCTTTC[A/G]GAAAGGGGATTAAAA | 23607 |
rs148992328 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47571777 | TTCTCTCTAGATTTC[A/C]GAGATTTTATTGACT | 23607 |
rs148993728 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47533268 | ATTTACTATCTGGCA[C/G]TTTATAGAAAGTTTG | 23607 |
rs149003300 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47586503 | AAATAATGGCTGAAA[A/T]TTTTAATTTGATGCA | 23607 |
rs149008871 | in-del | -/CTAT | 0.00835141 | 0.0640778 | intron-variant | CD2AP | GRCh38.p7 | 6:47513372 | AGTCTAAGTTATTGC[-/CTAT]CTATCTATGTAGGTT | 23607 |
rs149054320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47548384 | ATATTACAGTTGACA[C/T]CACAGAAATACAAAA | 23607 |
rs149078170 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47601057 | ATTTTTTTTAAAATT[G/T]AGGTAAATTACAACA | 23607 |
rs149130383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47561240 | TGTACAGAACATTTC[C/T]ATCACCCCCAAAATA | 23607 |
rs149184452 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47566620 | TCTCCCTTCCCCCGC[G/T]CCTCACCCCTCAACA | 23607 |
rs149194202 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47622803 | AAATACACAATGCGA[C/G]TCTCCGCATGCTGTT | 23607 |
rs149222793 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | CD2AP | GRCh38.p7 | 6:47537019 | CCTTAGTAGTGGAAA[C/G]TCACGCTACAGCAGA | 23607 |
rs149236155 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47563602 | TTTGTGTACAGTATT[A/G]TGCTCTACCATATAT | 23607 |
rs149246024 | snp | A/T | 6.72337e-05 | 0.00579761 | missense | CD2AP | GRCh38.p7 | 6:47533747 | CACAAACCAAAAACA[A/T]TAAGAAGAGTATGTA | 23607 |
rs149300022 | snp | C/T | 1.65244e-05 | 0.00287436 | missense | CD2AP | GRCh38.p7 | 6:47595900 | AACCTTCTAAACCAG[C/T]AGCTCCACAAGTCCC | 23607 |
rs149303011 | snp | C/G | 0.000421603 | 0.0145129 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624247 | TGTGGACCTGGTGTT[C/G]ATAATGTTCCAGGGA | 23607 |
rs149307604 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47484670 | AATATTATGTAGCTT[C/G]TTAAACTTCCCATCA | 23607 |
rs149371059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47498977 | ATGGCTTATTTTATT[C/T]GATGGGGTATATTCT | 23607 |
rs149425838 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CD2AP | GRCh38.p7 | 6:47504635 | TCTGCAGTTGTGGAG[C/T]CTGCGGATGTGGAGG | 23607 |
rs149469132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47527911 | GTCGTCTTTACCTAC[A/G]TTTGTTTTTTGGTTC | 23607 |
rs149512334 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47533911 | TGCCCTGTGTAGTCA[A/G]TCTTAATTTTTAGTC | 23607 |
rs149534363 | in-del | -/AAAAC | 0.0232847 | 0.105357 | intron-variant | CD2AP | GRCh38.p7 | 6:47514539 | CTTTGTAATTGAGAT[-/AAAAC]AAAATAAACACATTC | 23607 |
rs149535230 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | CD2AP | GRCh38.p7 | 6:47588923 | GAAACTTATAAGAAG[A/T]ATACTATTTACTGAT | 23607 |
rs149583133 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47550878 | TGATTTCATGGCATT[C/T]GCAGCTACCTGGATG | 23607 |
rs149606514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47604301 | GCACTGTTCCATTTT[A/G]CTAACCTAATGGCTT | 23607 |
rs149649083 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CD2AP | GRCh38.p7 | 6:47612613 | CCCAACTGGGTAATC[A/G]GTTCCTGTACAAATT | 23607 |
rs149666824 | snp | C/T | 0.029116 | 0.117091 | intron-variant | CD2AP | GRCh38.p7 | 6:47495912 | AACTTTACTCTCTTA[C/T]ACCATACAAGGATCT | 23607 |
rs149689745 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47554328 | ACATTCCAGAAGCTA[G/T]GTACTTCTTGCTGTT | 23607 |
rs149743420 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47561147 | ACTTTATTGGAGGTA[A/C]AATTTACATACAGTA | 23607 |
rs149763215 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47523749 | TATAAGGATTTACAT[C/T]TGATAAAGTGTACTC | 23607 |
rs149773344 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47581208 | AACTAGTTATTCTAC[C/T]GTTTCAAATGAAATC | 23607 |
rs149829490 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626991 | TAACTGTTACGTAAT[A/G]CAGTTGATGTTGTAA | 23607 |
rs149830580 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47585565 | AAGCCAAACAGACCT[C/T]GATGTCCTACAGAGT | 23607 |
rs149876024 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47596996 | GAAGAATATAAACAT[A/G]TTGAAAGCTGGATAT | 23607 |
rs149893360 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47600418 | ATTATAAAATATGCT[A/G]TTACATTTCAGGGTT | 23607 |
rs149899488 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47550527 | GCAAGAATGACCATT[-/A]AAAAAAAAAATAGAT | 23607 |
rs149921469 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47516824 | AAATAGGAAAGTCAT[A/G]GACAATCAACTGTTA | 23607 |
rs149963997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47565380 | AGAGGGTCTTTTTGT[C/T]AACATGCAGATTCCA | 23607 |
rs149984217 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47531323 | AATGTTTATATTTTA[A/G]CAATTTAACCATTTA | 23607 |
rs149993734 | snp | A/T | 0.000148597 | 0.00861838 | missense | CD2AP | GRCh38.p7 | 6:47574224 | AAGAACATCCAGTAG[A/T]GAAACAGAAGAGAAA | 23607 |
rs150046838 | snp | A/G | 5.07481e-05 | 0.00503701 | missense | CD2AP | GRCh38.p7 | 6:47599422 | TTTGATTCACTTACA[A/G]TAAGGACCTCCAAAG | 23607 |
rs150093624 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47533559 | GGATTTAATATAAAA[A/C]ATATAACTTAACTTG | 23607 |
rs150143950 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CD2AP | GRCh38.p7 | 6:47541001 | AGTTTTCCTATAGCA[C/T]GCAAAAAACTATTTA | 23607 |
rs150226591 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47571700 | TGTGAAGAAAGAGCA[A/G]TTACTAGGGGTTAAT | 23607 |
rs150251936 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47508546 | TTTCTTTTTTTTTTT[G/T]TTTTTTTTTTTTTTT | 23607 |
rs150300952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47583419 | TTCTTTATTCTACCT[A/G]TTCATCTGTCCTTCC | 23607 |
rs150304098 | snp | A/G | 0.000989446 | 0.0222203 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47580869 | ATTTTAACAGAAACC[A/G]AAGAAACCACCACCT | 23607 |
rs150354627 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | CD2AP | GRCh38.p7 | 6:47588730 | TGCCATCCTCAGTGT[A/G]CACTTTATCTTCAGA | 23607 |
rs150356497 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47491400 | AATTTTTTATCTTAT[A/G]CTGAAATATATTTTT | 23607 |
rs150373676 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47507008 | CGTTTCAAACCCTCC[C/T]TCTGCTTTGTCAACT | 23607 |
rs150416888 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | CD2AP | GRCh38.p7 | 6:47603682 | TTCTACAGCTGTTCT[C/T]TTTTCCTGTTTTGTA | 23607 |
rs150436428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521263 | TTCTATTAGAAGTGG[C/T]ATAGTAGGCCAGGCG | 23607 |
rs150441663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47621649 | GAATGTCTGGTAGAA[C/T]TCTGCTGTGAATCCA | 23607 |
rs150526991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47605484 | AAGTAAGTTGGTAAT[C/T]CATGTAGCTTTTTCT | 23607 |
rs150529382 | in-del | -/TTC | | | intron-variant | CD2AP | GRCh38.p7 | 6:47505009 | GGTGGCTGTGGCAGT[-/TTC]TTTTTTTTTTTTTTT | 23607 |
rs150547313 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CD2AP | GRCh38.p7 | 6:47623936 | TAATTTTAAATGCTC[A/G]CATGACTTAACATTT | 23607 |
rs150548816 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47522724 | CAATTTTTTTCTCTT[C/T]GTTTAGAATACAGGT | 23607 |
rs150599316 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47529895 | TTTTACCACCCTTAT[C/G]ATCTTTCCCTTCCTT | 23607 |
rs150619018 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47498605 | GTGCCTTTGTTTTAC[C/T]TGTTTTGGAACATTT | 23607 |
rs150653725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47486541 | ATTTATTCATCTCTC[A/G]TTAGTTTGACCAGTG | 23607 |
rs150663215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47544766 | TGCTATGGATTTTAG[A/G]AAAATTAATTGTAAG | 23607 |
rs150681166 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47563472 | GCTTTTAAAGCTTCT[A/G]TCCAAAATTGACATG | 23607 |
rs150732047 | snp | C/G | 0.0524604 | 0.153226 | intron-variant | CD2AP | GRCh38.p7 | 6:47516714 | CCCATTTTTTTTTCA[C/G]TGTGAGTGACAAATG | 23607 |
rs150809624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47580240 | TTTATTATGTTTGTA[C/T]ATTACGGCTTATCAA | 23607 |
rs150809756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47479243 | CCTATCACTTTTTGC[A/G]GTTGAGAGTTGGTAC | 23607 |
rs150851309 | snp | C/T | 0.000329924 | 0.0128395 | missense | CD2AP | GRCh38.p7 | 6:47574204 | GGCTCTGTGAAACTT[C/T]GGACAAGAACATCCA | 23607 |
rs150873373 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47494302 | CTTCCTTGCTTTCTT[C/T]GGGTTTCCCTAAGAA | 23607 |
rs150893957 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47509120 | TCTGATTTCAGTATC[A/G]TTGTGTCTCAGGGAA | 23607 |
rs150896554 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47611535 | AGAAATTATTGCCAA[G/T]AAGTTAGTTTTGAAA | 23607 |
rs150909400 | in-del | -/CCC | | | intron-variant | CD2AP | GRCh38.p7 | 6:47529184 | TTAACTCTAGTACTG[-/CCC]CCCCCCCCCCCCCCA | 23607 |
rs150924939 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47554125 | ACCACGTTGCCCAGG[C/T]TGATCTCAAACTCCT | 23607 |
rs150955718 | in-del | -/GAAA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47485576 | AAAATTAGAAAGAAA[-/GAAA]TAAAAAAATGTAGTT | 23607 |
rs150959557 | in-del | -/A | | | frameshift-variant | CD2AP | GRCh38.p7 | 6:47574242 | AACAGAAGAGAAAAA[-/A]CCAGAAAAGGTGGTA | 23607 |
rs150980630 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47592779 | CACCTGGAGAAGTTA[C/T]GGAAACTCTGCATCT | 23607 |
rs151001550 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47615074 | AAGTATTTCATACTC[C/T]CTTCTGTTTTTTATT | 23607 |
rs151002171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47512212 | CCGGGAGTGGTGACA[C/T]GCGCCTGTAGTCCCA | 23607 |
rs151032143 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497243 | CTTTCCTTTTCCTTT[C/T]CTTTTTTCCTTTCCT | 23607 |
rs151064033 | snp | A/T | 0.0126979 | 0.078662 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626468 | TTTCTACGTGTGAGT[A/T]TAAAAGACAAAAGTT | 23607 |
rs151118470 | snp | A/C | 0.000297555 | 0.0121938 | missense | CD2AP | GRCh38.p7 | 6:47503439 | CTGACAATTTCGTTA[A/C]GGTAAGTATTTTCAG | 23607 |
rs151119697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47533426 | AAACTCATGAGTCAC[C/T]GTTACCAAAATGTGT | 23607 |
rs151139452 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | CD2AP | GRCh38.p7 | 6:47500658 | AATTAAGTATCCGCT[C/G]TTTTTCTGGTCTCAA | 23607 |
rs151172462 | snp | C/T | 1.64944e-05 | 0.00287175 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47579447 | AGGAGTATTTCCAGA[C/T]AATTTTGCTGTCCAG | 23607 |
rs151212342 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47564849 | TTATAGTAGAATGTA[C/T]ATTATATAAGTGTTT | 23607 |
rs151222079 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47620486 | CAGGTAGTGTGATGC[C/T]TCCAGATTTGTTCTT | 23607 |
rs151252450 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CD2AP | GRCh38.p7 | 6:47585321 | AAAAAAAAAAGGAAG[A/G]TGATGCATTTTTGTT | 23607 |
rs151267303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47519612 | TAGGATTGTTTGGTA[A/G]CAATTAGATTTTGTG | 23607 |
rs151277283 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47574967 | AGTATTTATTTGATT[C/T]GTGTAGCTACATCTC | 23607 |
rs151326788 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47582519 | TTGCTAAAAACCTTA[C/T]TGGTTTGTTGTGAAT | 23607 |
rs151333024 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47589415 | ATATACACACACATA[C/T]ATATACACAAATATA | 23607 |
rs151336776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47482923 | AGGGCTTGCAGATAG[A/G]TAGAGAAAGAAGTAT | 23607 |
rs180718902 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47549359 | ATTCAGCAAAGTTTC[C/T]GGGTACACAATTAAT | 23607 |
rs180722842 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47566082 | GTATACCTTTGTCTG[G/T]AATCCTCTTCTTCAA | 23607 |
rs180738016 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47495594 | GTAATAAATAGATCT[C/T]GTCCGTGACTCTCTG | 23607 |
rs180743715 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47515738 | ATCAGCATAGTTGAA[A/G]GATCTTAGCATTATA | 23607 |
rs180745589 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47532059 | AGCCTGGGCAACAGA[A/G]TGAGACTCCTTCTCA | 23607 |
rs180775705 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47591702 | TTACGTACAGTGTTG[G/T]TAATGTATTGCTATA | 23607 |
rs180791388 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47598935 | ATAATAAAAAAAATT[A/T]AAAAAAAAATACAGG | 23607 |
rs180806813 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47575239 | CATGGTTTTTGGGGT[A/G]GTGCTCTATAGCCAT | 23607 |
rs180809099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47620527 | CTTGCTTTGGCTATG[C/T]GGGCTCTTTTTTTGA | 23607 |
rs180810403 | snp | C/T | 0 | 0 | intron-variant | CD2AP | GRCh38.p7 | 6:47611545 | GCCAAGAAGTTAGTT[C/T]TGAAACATTATATAA | 23607 |
rs180960244 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47499010 | TAATTTCATTATTTT[G/T]ATGCTCAAAATGTCC | 23607 |
rs180970657 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47519020 | TCATTTATTTATTCA[C/G]ATATTTACTGAGGTT | 23607 |
rs180984590 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47529276 | TTCAGTGTCGTTTTG[A/T]TGTAATGTTGATGAA | 23607 |
rs181009394 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47511898 | CGGGGGTGGCTCACA[C/T]TTGTAATCCCAGCAC | 23607 |
rs181018196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47545795 | CTCAGGAAGCCACAT[C/T]CCTAGGAAAAGAGGG | 23607 |
rs181020178 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47490113 | CCTGAGTAGCTGGGA[C/G]TAAGGCATGTGCCAT | 23607 |
rs181054568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47560336 | TAATATTGATAATAT[C/T]GTTTATTCTGTAATC | 23607 |
rs181065343 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | CD2AP | GRCh38.p7 | 6:47616074 | AGGCATGAGCCACTG[C/T]GCCTGGCCTTTTTTT | 23607 |
rs181076895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47595109 | TTAATACCTATTTAT[A/G]AGCACCTGAAAGATC | 23607 |
rs181205331 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47546182 | CAAAACTTCAGGAAA[C/T]AATGGATGCACTTAC | 23607 |
rs181227171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47622809 | ACAATGCGAGTCTCC[A/G]CATGCTGTTCTGTCT | 23607 |
rs181228660 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47512593 | GCCCATTTCATTGTC[C/G]CTTTGCAGTGTGTTT | 23607 |
rs181231930 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47602940 | TTAAAGAAACACATT[A/T]TTCGATGGAAGCATT | 23607 |
rs181234892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47552925 | TATTTTTAAGTTACT[A/G]TAGTTTTACTTTTAT | 23607 |
rs181236555 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CD2AP | GRCh38.p7 | 6:47587789 | ATGGTAACTTTTATC[C/T]TATGTCCTCCTCACT | 23607 |
rs181240177 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47480070 | TTTGTGATTTATTTG[C/T]TGTGTTCTGTTTAGG | 23607 |
rs181240486 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47570008 | AATATTGATTGATTT[G/T]AAGTCCAGTTAAAAC | 23607 |
rs181240765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47529586 | TTTTTATTAATTTTA[C/T]TAAATGTATGTATAG | 23607 |
rs181252581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47519296 | AAAACACAGGAGAAT[A/G]CAGAGTAGATAAGGA | 23607 |
rs181291373 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47499192 | TTCCTAAAGAGTCCT[A/G]ATTCCTTTTAGTAGT | 23607 |
rs181300851 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47579790 | TTCCTGGAAGAAATT[G/T]TATTTTTATTTAATG | 23607 |
rs181380579 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47561932 | CACCACCACACCCAG[C/T]TAATTTTTTTGTATT | 23607 |
rs181395675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47535480 | CAAGTTTGGGGAAAC[C/T]TCTACTTTTGGATTA | 23607 |
rs181459683 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | CD2AP | GRCh38.p7 | 6:47595711 | ATATAACTTTAAAAT[A/T]AGTAAAACAGTGCAC | 23607 |
rs181485621 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47559987 | GAACCAGGACTTCTA[A/T]GAATTTGGGCTTTTG | 23607 |
rs181504470 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47480984 | CTTATTTGAAGTTTA[C/T]GTTTTTAGTGTCTAC | 23607 |
rs181505877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47594879 | TTTAGCTATGTGCTA[C/T]GATGTTCAGGTTTTA | 23607 |
rs181506052 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47511826 | GGACATTAAGGTGCA[C/T]GTTCATCCTGGCTAA | 23607 |
rs181510674 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47528993 | TCTTAGTGCATGGCA[A/G]CATCTGAGCAGTTGC | 23607 |
rs181512656 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47578032 | TCTGTCATCTCACAT[A/T]GTTACCTTTTTTGTT | 23607 |
rs181513905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47499975 | CTCAGGTGATCCACC[C/T]ACCTCAGCCTCCCAA | 23607 |
rs181516752 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47536112 | TTAAAGTACATGTGC[C/T]GCAAGGACTATATTG | 23607 |
rs181518246 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47545146 | AATATTTTAAAAATA[A/G]ATCATGGACAGGAGG | 23607 |
rs181535499 | snp | A/T | 0.040671 | 0.13668 | intron-variant | CD2AP | GRCh38.p7 | 6:47615808 | ATTTATTTATTTATT[A/T]ATTTATTTATTTATT | 23607 |
rs181622208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47489282 | AAGCGATTCTCTTGC[C/T]TCAGCCTCCTGAGTA | 23607 |
rs181627391 | snp | A/G | | | intron-variant, downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47604416 | TTACATGAGCATGGT[A/G]TATAATTTTGTAAAT | 23607 |
rs181649990 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520279 | TCAGTGGTAAAAATA[C/T]TTATAACAGTCAATA | 23607 |
rs181667356 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47553387 | AGTCTCACTATGTTG[C/T]CCAGGATGGAGAGCA | 23607 |
rs181669205 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47570871 | TGATTTAATAGCAAA[C/T]GTGGTAGTAAAATTT | 23607 |
rs181679761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47524115 | ATATAAACCATGTTA[A/G]TGTTTGCCTTGGACT | 23607 |
rs181686163 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47620743 | GTTTTGTAGTTTTCC[A/T]TGTAGAGGTCTTCTG | 23607 |
rs181692563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47549564 | CTGAAAGAAATAGAC[A/G]ACAAAAACAAATGGA | 23607 |
rs181693928 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47599915 | CTTTTGCTAATTTTT[G/T]TTTAAGCTTTAGGAC | 23607 |
rs181702977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47484823 | CGTCCAGATAATTCC[A/G]AGGGAGTGACTGTAA | 23607 |
rs181715696 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47585143 | CTAAAAATAAAATAA[A/T]AAAAAAAAAACCAGC | 23607 |
rs181715910 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47566444 | TATATGTAGAACTTT[C/T]CAAACACTTTTGTCA | 23607 |
rs181719212 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47504835 | ATTGAGAGTGCAATC[A/G]CATTATATTAAAAAA | 23607 |
rs181738589 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47588133 | TACTTCTCTCAGAAT[C/G]TTTCATGGCCAGGTT | 23607 |
rs181782358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47623253 | CTAATCGTTTAATAA[C/T]GTGCTGTTTGTCGAA | 23607 |
rs181825557 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47496067 | CTTCTTTTGTTTTTC[C/G]TTTCTTTTCTACATT | 23607 |
rs181846829 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47556595 | CTCAGGTGATCCACA[C/T]GCCTCGGCCTCCCAA | 23607 |
rs181880268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47590673 | CGTGAGGATCTTAGC[A/G]CCAATCCTCTGTATA | 23607 |
rs181894615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47532524 | CGTTTTTCTTGCACA[A/G]TGTATTTTAAGATTC | 23607 |
rs181903966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47506993 | AAAATTGTAGTCAGT[C/T]GTTTCAAACCCTCCT | 23607 |
rs181924499 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47556993 | CAGCATCTGTTGTTT[C/G]CTGACTTTTTAATGA | 23607 |
rs181927058 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625486 | GAGTTACTTATGAAC[A/G]GTTGAATGCTTTAAA | 23607 |
rs181930384 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47575141 | CACTTTCTATCCTAC[A/G]TATTCCTAGCTCTGA | 23607 |
rs181947182 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47590920 | GACACACAAAAAAAT[A/G]GAAAAATATTCCATG | 23607 |
rs181950171 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47524914 | ACACTTAGACGATAC[A/G]TACTGATTTCATATT | 23607 |
rs181953093 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47539688 | AGTGAGTGTTAATGC[G/T]TTGTTGTGTGGGAGA | 23607 |
rs181977741 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47610435 | TAAAAAGTATAAAAG[A/G]ACAAAAAATAAAAAT | 23607 |
rs182057981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47515118 | AGGAGTACTGAGTGC[A/G]TTGTAGGTCTGGCAA | 23607 |
rs182073986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47486205 | AAATAAAAGTTTTGG[C/T]GCCTTGAGTAGTTTA | 23607 |
rs182093635 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47539331 | GGGTTGTCAAGCAGA[A/G]TATATTGAAGCTCTT | 23607 |
rs182105388 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47517002 | TAATATGGGAGGTGG[C/G]GCCTGGTGGGAGGTG | 23607 |
rs182131449 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47609727 | CTGGTATGAGCAAGT[A/G]TATTTTCAAAGAAAT | 23607 |
rs182136813 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476278 | TGAATTATTGCCTTC[C/T]CCAAGCTTTCGTTCA | 23607 |
rs182153004 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CD2AP | GRCh38.p7 | 6:47548941 | CACATAAACAGAATT[A/G]AAAACAAAAATCACA | 23607 |
rs182173998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47573738 | TCGTGATCTGCCAGT[C/T]TCAGCCTCCCAGAGT | 23607 |
rs182182687 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47567734 | AAGATCCTGAAAGAG[A/T]TTTAATTCAGAGGCA | 23607 |
rs182204341 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47518057 | TTTGTGTCAGGTGTT[C/G]TTGGGGGAGGTTCTG | 23607 |
rs182237295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47586221 | CAAAAACTGGAAAAT[A/G]TAAGAAAGACCCAAA | 23607 |
rs182242067 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47533901 | TACTAGTTATTGCCC[G/T]GTGTAGTCAATCTTA | 23607 |
rs182247058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47550300 | AAATCTTCACAATCT[A/G]TACATCTGACAAAGG | 23607 |
rs182352027 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47495453 | ACCTTGATTTTGCCC[C/T]CTCGCCTCCCGAAAG | 23607 |
rs182361318 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47531791 | ATAAGAATCCTTTTC[A/G]GCCGGGCGTGGTGGC | 23607 |
rs182406139 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47481317 | GCTCTCGTATATAAA[A/G]CATATCAGTCATGTG | 23607 |
rs182407721 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47500712 | CAAATTCTCATTAAA[A/G]AACATCCAGAGTCTG | 23607 |
rs182409243 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47508125 | TGCATTAGTCCCTAG[A/C]AAGAGAGTGAGCCTG | 23607 |
rs182427037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47565448 | CCTTATTTTATGAAA[C/T]CAGTGACTGTATATA | 23607 |
rs182442128 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47571743 | TGGTATGCTTATACA[A/C]GGCCAAGAATTGAGT | 23607 |
rs182445277 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47540434 | CCTCAATTTATGAGT[A/G]AACCCTATTTAAATA | 23607 |
rs182467929 | snp | G/T | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520824 | GCCAGTCTGCCTGTT[G/T]CCTGGTCATTTGGCT | 23607 |
rs182474706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47588367 | TTGGTTCTCTAATGC[A/G]TTACACAATAGGTAT | 23607 |
rs182486381 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47537244 | GTGCTGAAGAAAATA[G/T]TAACATTCTGAATGC | 23607 |
rs182491903 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CD2AP | GRCh38.p7 | 6:47553503 | AGGTGTGCACCACCA[C/T]ACCTAGTGAATTTTT | 23607 |
rs182498414 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CD2AP | GRCh38.p7 | 6:47600469 | CCCTCTTTCAGTTTG[C/T]GAATGCAAAGTTTCT | 23607 |
rs182500041 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47586427 | TCAAGTGGTTTTACT[C/T]ACCTGTAATTGGGGT | 23607 |
rs182526839 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47568115 | GAAAAAGAGGAGCCA[A/C]CTGCTACCAGGTTTT | 23607 |
rs182533227 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47621846 | AATGATGTTCATAGT[A/T]CCCTTGAATGATCTT | 23607 |
rs182538491 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47600646 | CATTGAAATTTATTC[A/G]GTATGTTTTATATGG | 23607 |
rs182558270 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47491590 | AAAAGTAAACATTCT[A/G]TAGTCAATGCCCATA | 23607 |
rs182678064 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47526137 | ATACCTTAGGTACTA[A/G]GTAAAGTTTGCTATA | 23607 |
rs182706582 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47487288 | GGCTGTGTTTCAAAT[C/G]TCAAGTTAGCCCTTT | 23607 |
rs182721809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47530545 | TCATTTTTATTGCTG[A/G]GTAGTGTTCCATTGT | 23607 |
rs182722763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47589054 | TGCAATTTAGGTTCT[A/G]CTTTGACATCTTGTT | 23607 |
rs182739394 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CD2AP | GRCh38.p7 | 6:47564153 | CCATTAGAGAACATA[C/T]ATAAGTACCAAAAAC | 23607 |
rs182750027 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626257 | GAATAGAAAAGTAAC[C/T]GAAATACTTTTACCT | 23607 |
rs182753014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47571962 | GTAGAACTTCTCAAC[C/T]TTGTCACTGAAGATG | 23607 |
rs182760421 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47606871 | ATTAAATTATTTTTG[A/G]CTAGTAGTTACCCTG | 23607 |
rs182763213 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CD2AP | GRCh38.p7 | 6:47557435 | TATTGACTAGGTTTT[C/T]TTCTAGGGTTTTTAT | 23607 |
rs182765815 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47492099 | TTTGAAACTTTGACC[A/G]TTTTACTTTAAGTTT | 23607 |
rs182793706 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47593770 | TTCAGAAAGTTAAAC[A/T]TGGAATTACCATATG | 23607 |
rs182808889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47621281 | GTTGTCGAATGTTTT[C/T]TCTGCATCTATTGAG | 23607 |
rs182825670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47617572 | TGCCCATATAGTCAT[A/G]TAGACATGGTACCTT | 23607 |
rs182825888 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47530023 | GACACTCTTCCTATT[G/T]CCTTCTCTGTACCTT | 23607 |
rs182827488 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47546847 | TCAGCAGAAACCATA[A/C/T]AAGCTAGAAGGGATT | 23607 |
rs182832777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47502219 | CAGCATAGCAGCTTG[C/T]GTCTTCAAAGCGAGC | 23607 |
rs182833071 | snp | C/T | 3.29897e-05 | 0.00406125 | missense | CD2AP | GRCh38.p7 | 6:47596008 | AAAAACCAGTTCCTC[C/T]ACCACCTCCTATAGC | 23607 |
rs182834815 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521944 | TGCTTGAACCTGGGA[A/G]GCGGAGGTTGCAGTG | 23607 |
rs182839313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47562800 | CTGTGATGAGCCTTT[A/G]TATGTCAAGTTGGTG | 23607 |
rs182842726 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47580411 | CCAAAGAGTTAAGAG[C/T]GAAAACTAAGTCTAT | 23607 |
rs183007251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521117 | GGAAGAATAGGGAAA[C/T]ACCTACTCCATCTTT | 23607 |
rs183012683 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47547081 | GAACCTCTTTGAAGC[A/G]TAAATCTCACAGGAC | 23607 |
rs183013420 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47541134 | CTTTTTCCTTTTTTT[A/T]ATTTTTTGAGACGGA | 23607 |
rs183024229 | snp | A/G | 0.000496524 | 0.0157485 | intron-variant | CD2AP | GRCh38.p7 | 6:47606125 | TACCTTTAAAAAGGT[A/G]CAGTTCTCTTAGTAA | 23607 |
rs183045524 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CD2AP | GRCh38.p7 | 6:47487563 | GGCATGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT | 23607 |
rs183047152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47508850 | CCTCACACTTTCTTC[A/G]TATCAGCAATAAGAC | 23607 |
rs183052931 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47481801 | ACTTATTTTTAGAGA[A/C]AAGGTCTTGCTCTGT | 23607 |
rs183054781 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47526557 | TATGTCCCAGAGAAA[A/G]TTGAAGGTTCCTAAA | 23607 |
rs183078055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47612111 | AACTTGCCTTGTATT[A/G]TGATGTGTTGATATT | 23607 |
rs183085722 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47554084 | TGCCCAGCTAACTTT[C/G/T]GTATTTTTTTTAGAG | 23607 |
rs183092841 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47550879 | GATTTCATGGCATTC[A/G]CAGCTACCTGGATGA | 23607 |
rs183127249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47618889 | TTTTACCCTGTATTT[A/G]TAAAAGCACACCTAA | 23607 |
rs183129840 | snp | C/G | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624679 | TAAGGGATATAAACT[C/G]TGTGTGTGTGTGTGT | 23607 |
rs183262493 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | CD2AP | GRCh38.p7 | 6:47527448 | TTTGGTGAAAGAAAG[G/T]AAAGGGAGAATTATA | 23607 |
rs183279962 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47501485 | CTGGGGCTGAGAGAA[G/T]CTTCGCCTGTAAAGT | 23607 |
rs183294840 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47537626 | CTACAGACATAATAC[A/G]TTACCTCTGATCACA | 23607 |
rs183301410 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47513632 | CTTTCTAATCTCTGC[A/G]TAGTATTCCATTGTC | 23607 |
rs183343353 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47572339 | TATTTACATGGTGCG[A/G]CATTTGTCAAACATT | 23607 |
rs183347806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47597249 | TCATGGAGAAAGCAG[C/T]AGACGAAGAGGTGAA | 23607 |
rs183354325 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47612738 | AACTGGAGGTCATTA[C/T]GTTAAGCCAGGCACA | 23607 |
rs183355639 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47542227 | GCATGTTTTCTTCTC[A/T]AGTTCTGTTAAGTGT | 23607 |
rs183361011 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47558722 | TGCTGGATTTGGTTT[C/G]CCAGTATTTTATTGA | 23607 |
rs183361402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47593876 | TATTTACAGTAGGCA[A/G]AAGGTAGAAGGAATC | 23607 |
rs183369168 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47576092 | TTTATTGTAGTTTTT[A/G]GAGATAGGGTCTCAC | 23607 |
rs183373612 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47538055 | TGCTCCGGGCAAGAA[A/G]ATTTTTTAAAAAGAT | 23607 |
rs183389426 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47607887 | TACCTTTTCTTTTCT[G/T]TGGTCTATTATGTCT | 23607 |
rs183410731 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47496720 | CTATTCTCATTCTCC[A/G]TAGGGAAACCACTGT | 23607 |
rs183508550 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | CD2AP | GRCh38.p7 | 6:47491823 | AATACTGATTTTTTT[A/T]AAAAAAGTTATTAAC | 23607 |
rs183544694 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47499144 | TCCAGGCTAATCTTA[C/T]ACTTTTCCTGCTTAG | 23607 |
rs183573915 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47554593 | TTTCCCATAGGGTGA[C/T]GATTTTCACTTAACA | 23607 |
rs183588342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47613192 | TCATCTTCCAAAATA[C/T]TGACATTTTGACTTT | 23607 |
rs183597851 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47558387 | GATGAGAGAGGACAT[C/G]CTTGTCTTGTGCCGG | 23607 |
rs183606600 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47535115 | GATTGCATACTTATT[A/G]CTATGGTCAATTTGA | 23607 |
rs183611836 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47551970 | TTATTGCCCTTTACA[A/G]ACTAGCATCTGTTGG | 23607 |
rs183613398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47602592 | ATTTTCTATGATTAA[A/G]AGGCAATTTCATGCC | 23607 |
rs183617912 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47568820 | GAGTGAAGAAAAAAA[A/C]TAAAGACCCTGGGAT | 23607 |
rs183619716 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47587739 | TGTGTAGAAGAGAAT[A/G]TAACAAAGGTGCTGT | 23607 |
rs183641635 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47589461 | ACAAATATATATACA[C/T]ATATACACACACATA | 23607 |
rs183648348 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47596851 | ACTGTTTTCCATAAT[A/G]GCTGTGGGAATTTAC | 23607 |
rs183759634 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47503826 | AGTAGCCCCATTTTA[A/G]ATATCTTGATATTTA | 23607 |
rs183772627 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47522663 | AGCTGACAAATGAAT[A/C]AAAATCACTCAGATG | 23607 |
rs183827695 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47575578 | GTTGGGGAAAACTAA[A/G]GTAAGTATTTTAGAA | 23607 |
rs183860883 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47618070 | ACACCTGTAATCCCA[C/G]CACTTTGGAAGGTCA | 23607 |
rs183871483 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | CD2AP | GRCh38.p7 | 6:47581610 | GTGGTAGCCACTAAC[C/G]ATGTGTGGCTTTTAA | 23607 |
rs183905543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47549850 | CAGCATGGTACTGGT[A/G]TAAAAATAGGCATAT | 23607 |
rs183928149 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47517175 | CTATGTGATGCGCCT[C/G]CTCCCCTTTCTTCTT | 23607 |
rs183949430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47585330 | AGGAAGGTGATGCAT[C/T]TTTGTTACTTTTATC | 23607 |
rs183972088 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47559841 | CTGTGGTAGAAAAGA[G/T]CATGAAGCAATAGAG | 23607 |
rs184005389 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | CD2AP | GRCh38.p7 | 6:47528762 | AGAGGCAAAGGATGT[C/G]TCACCTATCTTTTTT | 23607 |
rs184009436 | snp | C/G | 1.66815e-05 | 0.00288799 | intron-variant | CD2AP | GRCh38.p7 | 6:47544728 | AAAAAATGTGTTACA[C/G]GTAAAACAGTAATGG | 23607 |
rs184060361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47533819 | ATTTTATAACTGTGT[C/T]TAAATTAAGAAAAAT | 23607 |
rs184065472 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47509353 | GACAAAAATGTAATA[A/C]AGAGACATAAAGGGA | 23607 |
rs184085283 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47609610 | AGGCTGAGGTGGGAG[A/G]ATGTCTTGAGCCTGG | 23607 |
rs184097982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47590473 | TAAAGAATATGGTTG[A/G]CTCTTGAACAACATG | 23607 |
rs184121600 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47566714 | GTGAGAACATGCAGT[A/G]TTTGGTTTTCTGTTC | 23607 |
rs184198092 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47493144 | TAAAAAATGTATTTT[C/G]TTTTATCTTCATTTA | 23607 |
rs184221001 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47479618 | GGCATATTCTTTTAA[A/G]TATGAAATTATAAAA | 23607 |
rs184221375 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47564656 | TTTCCCCAACTCTAA[A/G]TTTTAGGCAAGTTTC | 23607 |
rs184222017 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47482805 | ATTCATAATTCAGAT[C/G]TGTCAGAGAATCCTG | 23607 |
rs184225400 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47542718 | TCTCAGGTATTTTGT[C/T]ATAGCAGCACAAATA | 23607 |
rs184251966 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47514071 | AGTTAATTTCTAGTA[C/G]TTCTTAATGTATTTT | 23607 |
rs184252163 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47531122 | TTGATATCATACTAA[G/T]ATAATCAGCTTTTAA | 23607 |
rs184264481 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47547661 | GAATTTAAACTATAC[C/G]CTGGAACAAATGGAG | 23607 |
rs184296431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47509760 | TATTAGACAAATCAC[A/G]TAATTTCCCTGTTTT | 23607 |
rs184327199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47576651 | TAGTAGAAACATACT[C/T]AAATGTATTAAGAGA | 23607 |
rs184360895 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CD2AP | GRCh38.p7 | 6:47527943 | TACCTGTAAATATAT[A/G]TTTGTGTCATATTGT | 23607 |
rs184389176 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47559067 | GGAAGGTTTATGTGT[C/T]CAGGAATTTATCCAT | 23607 |
rs184397953 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47488824 | TGAGCCTGGAAGGTC[A/G]AGGCTACAGCGAGCC | 23607 |
rs184433175 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47594397 | CAGGAATGATGAGTC[A/G]TATTTTTGTTACCTT | 23607 |
rs184459424 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47547979 | TTCTTCTTACTGAAC[A/G]ACAATAGTGACACAC | 23607 |
rs184487559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47597948 | CCAGTGGTGTCTCTT[C/T]TTACCACATGCAGCA | 23607 |
rs184493345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47583822 | AGAGTATATTGAGTT[C/T]TGTAGGCGCAACTGC | 23607 |
rs184516894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47564844 | AAAAATTATAGTAGA[A/G]TGTACATTATATAAG | 23607 |
rs184523034 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47619372 | ATAATAGTCTCCAAT[G/T]TCATGCAGGTCACTG | 23607 |
rs184549735 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47495456 | TTGATTTTGCCCTCT[C/T]GCCTCCCGAAAGAGG | 23607 |
rs184551418 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47608952 | AATGATTACAAATGT[A/G]TTCTTTAGTTGTCTG | 23607 |
rs184555266 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47555988 | AAAACATAAAGTTGG[C/T]ATAGCAAATGGGTTT | 23607 |
rs184558708 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47589971 | GGATTTTTACTATCC[C/G]TACCTTAGCTTACTG | 23607 |
rs184560212 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47572916 | CCTATTGTTCTTACT[C/G]TTATTTTTTAACAGA | 23607 |
rs184579164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47594589 | TAGAAATTTAAGTTT[A/G]GCTGGTTGTTATAAC | 23607 |
rs184642752 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47483462 | AGGCCTTGAAAACCT[A/T]GCCACAGGGAAACAA | 23607 |
rs184699894 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47510808 | GGCCGGGCGCGGTGG[C/T]TCATGCCTGTAATTC | 23607 |
rs184700041 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47489017 | CTGCTGCTGTTCTTA[A/C/G]AAGTTCTTGTAGTTG | 23607 |
rs184755451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47615522 | ACACAGTTCATGTGG[C/T]GAGAGAGGGAGTAAG | 23607 |
rs184777093 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47498881 | AGTATTTTAGTGTGT[A/G]TTTTTAACAAACCAG | 23607 |
rs184783410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47518744 | ACATTTCACATTTCC[A/G]TCAGCAATGTATGAA | 23607 |
rs184831251 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47523288 | TTGGAATATTAAATG[C/G]AAGACAAGTTTACTG | 23607 |
rs184840404 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47556374 | TCATGACCCTCCAAA[A/G]GACATGAACTCATTC | 23607 |
rs184854841 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | CD2AP | GRCh38.p7 | 6:47484054 | TAGAAAGACCTTTTT[G/T]GTTGTTGCTTTTTAA | 23607 |
rs184864661 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47582524 | AAAAACCTTATTGGT[G/T]TGTTGTGAATTTGGA | 23607 |
rs184946739 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47539178 | TTCTTGTAGGCTATA[A/G]GAGGCATTAACATGT | 23607 |
rs184973776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47504091 | GCCAGAAAACAATCT[C/T]TAGGGCTCTTATCAA | 23607 |
rs184980600 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47545265 | ATATGTTAGGAAAGC[C/T]GAGAGAACCCACAGA | 23607 |
rs185000485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47490343 | TTTACTTACATACCC[A/G]AAAGTTTTCCTAGAG | 23607 |
rs185011692 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CD2AP | GRCh38.p7 | 6:47573527 | GGAGTCTTGCCCTGT[C/T]GCCCAGGCTGGAGTG | 23607 |
rs185013766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47594922 | TCTGGTTGATATGAA[A/G]TCTTACAGAATTATT | 23607 |
rs185022100 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47578179 | TTTAGAAGAAACTTA[C/G]AAGGTCTTGTTAATT | 23607 |
rs185041716 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47560163 | CTTTACCCTGATTTA[C/T]GAATTTTTAACATTT | 23607 |
rs185050869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47615925 | GCTAGGACTACAGGC[A/G]CCCGCCACCACACCC | 23607 |
rs185082814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47514992 | AGGAGGCGGAGGTTG[C/T]AGTGAGCCAAGATCA | 23607 |
rs185145410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47609955 | CTTAGTTTTCAGAGG[A/G]TTTGATCACTGTTTC | 23607 |
rs185202539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47531521 | CAGCTTTTTGGATAT[A/G]AATCCACTGAGCCAG | 23607 |
rs185225404 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47495309 | CAGTGGAACAGTCAC[A/G]TCAAGATGGAGGTAG | 23607 |
rs185269060 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47590725 | TGGGAAGGTCTTATG[G/T]ACATGTAATTGGAGG | 23607 |
rs185274443 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520933 | TCTCCAGTACCTAGC[A/C]TGGGATATAGGCAAA | 23607 |
rs185277517 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47537540 | TCACCTACATATGCT[G/T]TTAACATTTTCTCAC | 23607 |
rs185280447 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47491726 | TTATAATATTGCCAC[C/T]AATATTTTTGCATGT | 23607 |
rs185286455 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47513018 | TAGTAGAGAGAAATG[A/C]TGTCAGGACAATGAG | 23607 |
rs185288650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47529651 | TTTTGATCTTTATTT[A/G]TAAGTTTGGTGATGT | 23607 |
rs185319241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47588657 | AGTCTAGAAGTAGGA[A/G]TCATATGACCTGCCA | 23607 |
rs185320954 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47580017 | TGGATGAGGAATATA[A/C/G]TAGAGTTTTTAGAAT | 23607 |
rs185326860 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47603409 | AAGTTGATTTAGTTA[C/T]AACTACATTATGAGA | 23607 |
rs185332152 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47534359 | AAGCAAAACAAAACA[A/C]AAAACACCAGGTAAT | 23607 |
rs185335860 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47587816 | CACTTCCTATACACA[C/T]ATACACAGTCATACC | 23607 |
rs185339764 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47553706 | CACTCCTTAATATCC[A/G]TATCAGAAACTATAC | 23607 |
rs185346091 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47571808 | ACATGGGCAATTCAG[A/T]AGAGAGGCGAAGTGG | 23607 |
rs185347144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47546615 | ACATATTTGGGGGAA[C/T]AATCAGAAAAACTTC | 23607 |
rs185354826 | snp | A/G | 0.0100561 | 0.0701919 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625649 | AATGATCATGCTTCC[A/G]TTTTTTTTAGTTTTA | 23607 |
rs185358147 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47561946 | GCTAATTTTTTTGTA[G/T]TTTTAGTAGTTACAG | 23607 |
rs185360746 | snp | A/G | 0.00042208 | 0.0145211 | intron-variant | CD2AP | GRCh38.p7 | 6:47606297 | GTTCATCTAATTGTC[A/G]TAAACTACAGTATAT | 23607 |
rs185361277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47497909 | TCTCCCGTTTAGTAT[A/G]GACTGTTTGTTCCTT | 23607 |
rs185364287 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47622821 | TCCGCATGCTGTTCT[G/T]TCTGGAGCCGCAATC | 23607 |
rs185378462 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47565614 | TCTTCCCCATCTGAG[A/T]TAAGGAGAAATTCAT | 23607 |
rs185411455 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CD2AP | GRCh38.p7 | 6:47531902 | ACATGGTGAAACTCC[A/G]TCTCTACTAAAAATA | 23607 |
rs185427977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47598587 | GTAAAAAAGATGGAA[A/G]AAATGGCATTCACAG | 23607 |
rs185448736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47518583 | TTTCAATTTCTGAAT[A/G]TCAGGGGTAAAGCTG | 23607 |
rs185486339 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47477189 | CAAATTATACTTTAA[A/G]AAGAAAAAAAGCAAA | 23607 |
rs185517855 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47584457 | GAATGTCTAGTTGAT[C/T]CAACACCGTTTGTTG | 23607 |
rs185519439 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47515427 | CTAATAACACTTTAT[A/G]TCTGTATGAATACTT | 23607 |
rs185521943 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47495921 | CTCTTATACCATACA[A/C/T]GGATCTTGGAACAAT | 23607 |
rs185536054 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47516407 | TTCATTTCATTGGCC[C/T]ATAGCAATGATGTGG | 23607 |
rs185542797 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47532139 | ACTTTTATAATCATA[A/G]GAATTTATAAACTTG | 23607 |
rs185545858 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47620221 | AGTCCTTAATCCATC[A/T]TGAGTTGATTTTGGT | 23607 |
rs185604407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47549442 | AAATCAAGAACTCAA[C/T]GCCTTTTACAATAGC | 23607 |
rs185606844 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47551489 | GTTGAAGCATTGTGC[C/T]GAGAGTTTCACATTT | 23607 |
rs185609509 | snp | C/T | 0.000441224 | 0.0148465 | intron-variant | CD2AP | GRCh38.p7 | 6:47599462 | AGTCAGCATGGACAG[C/T]GGTGGTGCATTTAAA | 23607 |
rs185611521 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47566323 | ATATATATATATATA[C/T]ACACATACACATATA | 23607 |
rs185617450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47584646 | CCTAGCTTTATCTTT[C/T]GTTTTACTTTCAAAA | 23607 |
rs185620261 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47529058 | TTCTTCTTAGGTTGT[A/G]TCTACTGAATTATCT | 23607 |
rs185629101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47586965 | GAATGTTCTCATACA[C/T]CTGATATGCCTTTAA | 23607 |
rs185664019 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47622365 | CCTGGAGGTCTCTCG[A/C]CCCGTTCAAATTGTT | 23607 |
rs185752000 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47568429 | AACTGGGGCTTGATA[A/G]TACTTTAGGTGGTAT | 23607 |
rs185780944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47534834 | AGATAGACTCTCACT[C/T]TGTTGTCCTGGCTGC | 23607 |
rs185802611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47601224 | TCTATCTTTTATACA[C/T]AGCTGTTATTTACTC | 23607 |
rs185841066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47566588 | GGTTCCTGCACCTAT[C/T]GACCCATCCTCTCAA | 23607 |
rs185870886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47620750 | AGTTTTCCTTGTAGA[A/G]GTCTTCTGACTCCTT | 23607 |
rs185879281 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47600113 | GTAGTGCTTTTTGCA[C/T]TTGTGTTTAGTTTTT | 23607 |
rs185885161 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | CD2AP | GRCh38.p7 | 6:47585252 | AGCTTGCAGTGAGCC[G/T]ATATTGCGCCACTGC | 23607 |
rs185906938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47545895 | TCTGACAGAGCCTAC[C/T]CAAATGAGAAGGAAT | 23607 |
rs185936527 | snp | C/T | 8.4023e-05 | 0.00648108 | intron-variant | CD2AP | GRCh38.p7 | 6:47579496 | GACTTTCCAGTAAGC[C/T]TTTGTTTTTCAATGA | 23607 |
rs185938855 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47512103 | GCGGAGCTTGCAGTG[A/G]GCCGAGATCGCGCCA | 23607 |
rs185970246 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47616652 | ATAGCCCCCATTTAG[G/T]TCTAGCTGCCTTCTT | 23607 |
rs186016860 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47484868 | TAGTAGAATGCAATC[A/C]TGAGCCCCTTAGGAA | 23607 |
rs186018841 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47505143 | TAAACAAGTGAACAA[A/G]GGTCTCGTTTTCCTA | 23607 |
rs186045837 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47560617 | ATTATATTTTATTGG[C/G]AGGACTATGGAGTGA | 23607 |
rs186071714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47524401 | CATGTTTTTTCCGTT[A/G]GAAGAAATTGTAAAC | 23607 |
rs186074587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47529399 | ACATCCCCAAGATGC[A/G]TACTTGAGGTTCATT | 23607 |
rs186078850 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47500832 | GCTCACTGCAACCTC[C/T]GCCTCCCGGATTCAC | 23607 |
rs186084218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47539476 | AAATCCAGTGTGACT[A/G]GACTGTATGAGCTAT | 23607 |
rs186107686 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47595370 | GGCTAAGCAGTCTTG[C/T]CCTAGTTTCTCTTAA | 23607 |
rs186162601 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47535573 | ATGACACTTGGACCA[A/G]TTCTAGGGTTCTATT | 23607 |
rs186177535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47570236 | GCAGTTCTTTTAAGT[C/T]ACTTTATATGAAGAT | 23607 |
rs186288794 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47525177 | TGTAAGCCTAAAATT[A/T]GTCAGAGCTAAAATA | 23607 |
rs186294576 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47539771 | GCCTTTGCTGTACCT[A/C]CTTTATTCTCTTCCT | 23607 |
rs186319313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47591177 | GAATCTTAGGATTTC[A/G]TTGACATAAAGTTAA | 23607 |
rs186319727 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47553020 | TTTCAAGCCCTTTCT[C/G]TTTGCTCCTAACAGC | 23607 |
rs186339752 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47480502 | AAAAGCATGGGCTCT[A/G]GACAGAGACTACTTG | 23607 |
rs186345151 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47575212 | GGTTTTAAAGGTAAA[C/G]TTTGGAATTCTCATG | 23607 |
rs186350912 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47519764 | TAAAATTAGTCAACA[A/C]ATTTTTTTGAATACC | 23607 |
rs186352878 | snp | A/G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47610602 | AGAACACTTTCACAG[A/G/T]TATTCCTTAGAAATA | 23607 |
rs186392207 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47617507 | CCAGTTAAATTTATC[A/G]TCTTCCTTTCCTGTT | 23607 |
rs186408368 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CD2AP | GRCh38.p7 | 6:47487342 | TCCTATATGGATTAT[A/G]TATTACAAAATGCAG | 23607 |
rs186420540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47617989 | CTGCTCAAACAATTA[C/T]CTTCATTAAATTGAT | 23607 |
rs186476544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47557728 | TTTTGGTTACTGTAG[C/T]CTTGTAGTATAGTTT | 23607 |
rs186478403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47481162 | GAAAGCAAATGGCAC[A/G]AAGTGTCAGAGCATT | 23607 |
rs186494051 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47620697 | GTGGGATGTGTTTTC[A/C]TTTGTGCTGTCTGTG | 23607 |
rs186496791 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | CD2AP | GRCh38.p7 | 6:47500151 | AATAGCTGTACTAGT[G/T]TTCCTAAGCTATTTT | 23607 |
rs186499690 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47526267 | ATGTGTGTGTTTCTA[C/G]TAGTAAGGGATTGTA | 23607 |
rs186518527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47591916 | TGCAACCTCAAACTC[C/T]TAGGCTCAGGTGATT | 23607 |
rs186535925 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520299 | AACAGTCAATATTGG[G/T]TGAGGACCTTGGATC | 23607 |
rs186538461 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47536256 | TTACTGTTTGGATCA[A/T]ATCTCTAATTCCCAA | 23607 |
rs186691353 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47575273 | ACAGCTAGGAATGTT[A/G]GACAAGCAATTCTTG | 23607 |
rs186702189 | snp | C/G | 0.00113381 | 0.0237827 | intron-variant | CD2AP | GRCh38.p7 | 6:47609097 | AATATTAAATAAAAT[C/G]AGAAATTTTTTTTTT | 23607 |
rs186706708 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47508162 | GAAGCCTTGAAGCTA[A/G]GCTTTGATTTCTTTC | 23607 |
rs186713925 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47590139 | ATGGCTAGAAACCAA[C/G]AACAACAGACAATGG | 23607 |
rs186714548 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47540619 | ACTTGGGAAAAATTA[C/T]GTTTAGTGTGAGAGG | 23607 |
rs186715696 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47549572 | AATAGACGACAAAAA[C/T]AAATGGAAACACATC | 23607 |
rs186731808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47611953 | GATTAGAAGGGAACA[C/T]GGGAAGGTGAAAAGA | 23607 |
rs186752964 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47517012 | GGTGGGGCCTGGTGG[A/G]AGGTGATTGACCCAT | 23607 |
rs186765022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47492165 | TTTCTATCATAATCC[C/T]TTCAAGCTGCTATGA | 23607 |
rs186765227 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | CD2AP | GRCh38.p7 | 6:47513893 | AAAAAATTTTTTTTT[G/T]GGGGGGGGGCTAGCC | 23607 |
rs186916836 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47532547 | TAAGATTCCATCTTT[C/T]CTCATTTTTTTCTGT | 23607 |
rs186947591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47496327 | GTTGCTAAGTCACCC[A/G]TTAGTCTGAATGTTG | 23607 |
rs186968698 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | CD2AP | GRCh38.p7 | 6:47556612 | CCTCGGCCTCCCAAA[G/T]TGCTGAGATTACAGG | 23607 |
rs186986249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47507542 | TCAAGCGATTCTCCT[C/T]GCCTCCCTAGTTCAA | 23607 |
rs187032882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47514329 | AATCATAAACTATAC[C/T]TCATTAATTTGTTAT | 23607 |
rs187034265 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47566954 | ATGTGTCTTTATAGT[A/G]GAATAAATCCTCTTA | 23607 |
rs187038413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47531172 | GAATTCTCATTTTCA[A/G]TTGCTATGCCAGAGA | 23607 |
rs187050574 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47547784 | ATAGGCCACAAAGTG[A/G]ACCTCAGTAAATTTA | 23607 |
rs187063154 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47493555 | TAGTTTTTTTTGTTT[A/G]TATCCTAATTTTGTT | 23607 |
rs187064939 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47600222 | GTCTAAACAAAGTAA[C/G]CTACAGACACATTAA | 23607 |
rs187076555 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47597275 | GTGAAGGAGGCTTAT[A/G]GGTAGAAGGCCCTCT | 23607 |
rs187078035 | snp | C/T | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47627132 | AATTAAAGGATTTTA[C/T]TGCCAGTCGTGTCAG | 23607 |
rs187083461 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47582676 | TGTAGTCTAATCCAT[A/C]CTTGTTTCTTGCCTA | 23607 |
rs187086605 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | CD2AP | GRCh38.p7 | 6:47607069 | GCAAAGTTTGTTCTT[C/T]TGTGCCAGGTTTAGT | 23607 |
rs187095686 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47564826 | GTTCCTCGTAGCTGT[A/T]AGAAAAATTATAGTA | 23607 |
rs187234390 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47486279 | TTTAAACTTCTCACA[A/G]CCCCTGGGTTCTGAC | 23607 |
rs187261315 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47518407 | TGGCAACCACTGATA[C/T]GCTTTTTGTCATTCT | 23607 |
rs187263685 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47585480 | GTATAAGTCACTGTG[A/T]CACTGAAGTGAGACC | 23607 |
rs187283986 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47534248 | GAGCATTACATTTGA[A/T]ATCAGATAAGGGTTT | 23607 |
rs187286255 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47621032 | GATTTGGATGCCCTT[G/T]ATTTATTTCTCTGCT | 23607 |
rs187288769 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47550445 | CAACAAACATGAAGA[C/T]ATGTTCAACATCACC | 23607 |
rs187304357 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47497568 | GGTGCGTTATCATTA[C/G]TCCTGACTACATTTT | 23607 |
rs187304573 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47489642 | AATGTACGGAGCATT[C/T]GGTTCCCCACAAGAA | 23607 |
rs187313075 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47600599 | CTACTAATTTCTGGG[A/G]ATTGAAATGTTGATT | 23607 |
rs187334202 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47508966 | GCTGTTGGTGTAAGG[A/G]CCTAGCTTTTGGCCT | 23607 |
rs187334413 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CD2AP | GRCh38.p7 | 6:47487644 | GCAGTGAGCTGAGAT[C/T]GCGCCACTGCACTCC | 23607 |
rs187335215 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47568012 | TAGAGGAGTGCTATG[A/G]GGATGGAGAGACACG | 23607 |
rs187339818 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47621545 | TTTGGTATCAGGGTG[A/T]TGCTGGCTTCATAGA | 23607 |
rs187345628 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47527146 | TGTTCTTTTAAAAAA[A/G]GAAAAGTTTTTTTGA | 23607 |
rs187354740 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47588138 | CTCTCAGAATCTTTC[A/G]TGGCCAGGTTTTTCT | 23607 |
rs187360772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47553452 | CCCAGGTTCAACTGA[C/T]TCTCCTGCCTCAGCT | 23607 |
rs187393492 | snp | C/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625055 | TTTAACCCTTAACTT[C/G]TGCCTAGAAACTACA | 23607 |
rs187400412 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47541370 | ACCTCATGATCCGCC[G/T]GCCTCGGCCTCCCAA | 23607 |
rs187403268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47558597 | TGCAGTTTTTGTCAT[C/T]GATTCTGTTTATGTG | 23607 |
rs187419588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47575849 | TAAAGAGTTTTTTTT[C/T]CTCCTCTTTCATTTT | 23607 |
rs187455284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47511840 | ACGTTCATCCTGGCT[A/G]ACACGGTGAAACCTC | 23607 |
rs187559267 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47621952 | TAGGGTGGGTAGGGA[A/G]GGGCCATCAGGTTGG | 23607 |
rs187578014 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47600906 | TTAAATTTTCACAAA[G/T]TTGGGGGATCTTTAT | 23607 |
rs187578936 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47570872 | GATTTAATAGCAAAC[A/G]TGGTAGTAAAATTTG | 23607 |
rs187591341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47481669 | GTTTTAATAGACAAA[C/T]TTGTGGTTGGTTTAG | 23607 |
rs187600647 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47542681 | AAGTGAGAAGTAAAT[G/T]TATACTATCTTCATT | 23607 |
rs187607817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47604659 | ATTTTAACATCTTTT[A/G]AAAATACTGATTGCT | 23607 |
rs187619262 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47558759 | TCGCATTGATGTTCA[C/T]CAGGGATATTGGCCT | 23607 |
rs187630934 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47581902 | TAAACCATGGTTTCA[C/G/T]CTGATGTTATTTTTC | 23607 |
rs187631235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47547336 | CATAAACTTAAAGAT[A/G]TAGAAAAAGACATTT | 23607 |
rs187656876 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47618578 | AATATATCTTAAATT[C/T]GCAGCATGTAATGTA | 23607 |
rs187674292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47612817 | TGAAACGATTGAACT[C/T]ATAGAGATAGAGAAC | 23607 |
rs187682185 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47594199 | GTAGATAAAGGTGGT[G/T]GTTGCGTAACATCGT | 23607 |
rs187691206 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47576155 | TCATAGCTCACTTAT[A/G]ACCTTGAACTCCTGG | 23607 |
rs187711469 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47496721 | TATTCTCATTCTCCA[C/T]AGGGAAACCACTGTC | 23607 |
rs187776595 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47517285 | AGCCAATTAAACTTC[C/T]TTTTTTTTTTTTTTG | 23607 |
rs187847668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47572242 | CAAGAAGCAGGGGCC[A/G]GGCGCAGTGACTCAT | 23607 |
rs187860246 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47501811 | AATATTAAAAATATG[C/G]TTATGTGATCCTATA | 23607 |
rs187861780 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47482888 | TACTTTAATGTATAT[A/G]AAAAATTGTAATTGT | 23607 |
rs187865496 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47503179 | CTTTGTGGTATTAAA[C/T]ATTGTTGCTAAACAG | 23607 |
rs187869825 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47522293 | AAAGTATTTTTATTC[A/G]CTGTACTTAAAAGAG | 23607 |
rs187873858 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47563013 | GAGTCCTTCAAATGC[A/G]AGAAATGAACAAATA | 23607 |
rs187882565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47537640 | CATTACCTCTGATCA[C/T]ATTATCTTTTTCTTC | 23607 |
rs187897754 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CD2AP | GRCh38.p7 | 6:47597180 | ATCCAGTCAGGGTTG[A/G]AACCATGGCAAACCA | 23607 |
rs187901897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47530661 | GTATTCTTTTGTAAA[A/G]TGTACAGTACTGTGA | 23607 |
rs187914715 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | CD2AP | GRCh38.p7 | 6:47564347 | TTTGTGATGCCATAT[A/T]AAACTGAGCCTTTAA | 23607 |
rs187919234 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47596453 | GGCTCTGGTAATCAC[C/T]ATTCTACTCTATTTC | 23607 |
rs187925681 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47580684 | TGTTTTTTCTAATGA[A/G]ATAATTTGTTGTCAT | 23607 |
rs187933171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47538327 | GCTCACTGCACCCTT[C/T]GCCTTCCAGGTTCAA | 23607 |
rs187939994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47555582 | CGGCTTAATGCAAAT[A/G]TATGAAAACTAAATA | 23607 |
rs187959660 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47622780 | TTCTTGCAGTCGGTC[C/T]GGAGTTAAAATACAC | 23607 |
rs187962029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47602860 | AGCCTTGATCATGCC[A/G]TTGCTCTCCAGCCTG | 23607 |
rs187971532 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47587784 | CTAAAATGGTAACTT[G/T]TATCTTATGTCCTCC | 23607 |
rs188076476 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | CD2AP | GRCh38.p7 | 6:47482472 | CAACCTCCGCCTCCC[A/G]GGTTCAAGCAAGTCT | 23607 |
rs188117734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47554371 | ATGGTTATCTGATAC[C/T]TTCATGAAAAGTACT | 23607 |
rs188140297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47589211 | GAACTTTTACTAAGA[A/G]TTTGTATTAAGTGTT | 23607 |
rs188156912 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521137 | ACTCCATCTTTCTGT[A/G]AGGGAAAATCTAGAT | 23607 |
rs188157979 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47539000 | AACTCTTGTGTGTCA[A/C/G]ATGCCTTTGTATCTG | 23607 |
rs188160481 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47594480 | TTATTTGTGTATTCT[G/T]TTAAAATAAATATAT | 23607 |
rs188167024 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47495463 | TGCCCTCTCGCCTCC[A/C]GAAAGAGGAGAATAA | 23607 |
rs188169186 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47556139 | TAGGTATACATGTGC[C/T]ATGGTGGTTTGCACC | 23607 |
rs188172992 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47559238 | ATTAGTCTGGCTAAC[C/G]GTCTCTCTGTTTCGT | 23607 |
rs188173508 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47515451 | AATACTTTGCATATT[C/G]ACATACGTTATCTCA | 23607 |
rs188179118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47573290 | TTACCTAATCTCTGA[A/G]CTAAAATAACAGATT | 23607 |
rs188180904 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47532030 | GTGACCAGAGATCGC[A/G]CTCAGTGCACTCCAG | 23607 |
rs188210362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47619047 | TACAAGTGCTAAAAG[A/G]GAAACTCTAGCAATG | 23607 |
rs188350825 | snp | C/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47477635 | CTGGACGCGGTCGGC[C/G]CGCGACCCCCGGCCG | 23607 |
rs188377783 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47551230 | TTTTTACATCTCTGC[G/T]TTTATCATTTGAAGG | 23607 |
rs188406432 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47586881 | GTTTTAGGGTAGATA[G/T]GAGAATTTTTTTGTA | 23607 |
rs188408921 | snp | C/T | 0.00676609 | 0.0577691 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47477036 | GCTTGCTGAAATAAT[C/T]ATACTTCTTCGTAAC | 23607 |
rs188410374 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47518685 | GGATTGCTGGGGTAT[A/G]TAAGAAACTGCAAAA | 23607 |
rs188412428 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47612164 | TTTCAGTTTTCCAAC[C/T]TGGAAAATGTATGAT | 23607 |
rs188419618 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47576697 | TGTTACACTGTCTTA[C/T]TAGAATAGCAAATTC | 23607 |
rs188441513 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47613732 | TAACAAGAGTCAGCC[C/T]GTCCTTTGAAGCTTT | 23607 |
rs188454010 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47542846 | GCACAAAAGAAGATT[A/G]TTTAATTTAGAAAGC | 23607 |
rs188498300 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47620704 | GTGTTTTCATTTGTG[C/G]TGTCTGTGATTTCTT | 23607 |
rs188512460 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47599799 | AGATGACATAGACTT[C/T]CAGTGCCAGCATTAG | 23607 |
rs188518688 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47584998 | CAGTCAGTTGTTCTT[A/G]TAAATAAATTGGAGG | 23607 |
rs188533548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47484415 | CTTCCTAGATGTTCT[A/G]CACTCTTCCTGACCA | 23607 |
rs188663931 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47533843 | GAAAAATTAGTTCAG[G/T]CTTTTGTAGACAACT | 23607 |
rs188667749 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | CD2AP | GRCh38.p7 | 6:47509603 | AATATTTAGAGCAAG[G/T]TCACTTCATTTTTTG | 23607 |
rs188670657 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47568136 | ACCAGGTTTTTGGCT[G/T]TGTAAGATGGAGATG | 23607 |
rs188692345 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47498450 | ATTGGATTCTCACAG[A/T]CCTGTTTCCATTTGA | 23607 |
rs188694021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47535295 | ATATTTAATCACATT[C/T]ACTTTAATGTCTTTG | 23607 |
rs188703341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47593806 | GCAGTTCCAAACGTC[C/T]AAGAGAATTGACAAC | 23607 |
rs188704094 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47552774 | AGTTTGGATCACTTC[C/T]AGTTCTTTGGTGCTT | 23607 |
rs188706253 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47534549 | CCATCTCTACTAAAT[A/G]TACAAATTAGCCGGG | 23607 |
rs188715589 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47569301 | CAGAAGGTGGAGGAA[A/G]TGCGTTTCACATTAT | 23607 |
rs188742919 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47519043 | CTGAGGTTCCTTGCG[C/G]TAGGACTTTTTATAG | 23607 |
rs188779376 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CD2AP | GRCh38.p7 | 6:47488873 | TCCAGCCTGTGCAAC[C/T]GAGTGAGTCTTTCTT | 23607 |
rs188881568 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47530091 | GTCACTTTCTCTGAG[A/T]AGTCATCCCGATTTG | 23607 |
rs188891452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47619404 | AGATGCTGTTAATTC[A/G]TTCCTTTTTATGGCT | 23607 |
rs188897621 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47598272 | TTAGCATGGATGCAG[C/T]GAAAAGGGAACACTT | 23607 |
rs188904531 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47491898 | CAGAACCAAGTTAAG[A/C]AAAACTTTTTTCTTT | 23607 |
rs188931160 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47488504 | CATAATGTATTCAGT[A/T]TAAAAAGTTATTAAT | 23607 |
rs188948000 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47550056 | CCTTATACAAAAATC[A/C]AATCAAGATGGATCA | 23607 |
rs188951935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47527666 | GATTTGGTATGGGAC[A/G]TGGAAGTAACTATGT | 23607 |
rs188970759 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CD2AP | GRCh38.p7 | 6:47589617 | AAGTAGGAGAGCTAC[A/G]AATAAAATGAAGAAT | 23607 |
rs189054355 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47623020 | GGAATAAAGACTTTA[A/G]TAACAGATCGGGCTG | 23607 |
rs189077994 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CD2AP | GRCh38.p7 | 6:47511043 | GCGCCACTGCACCCC[A/G]GCCTGGTGACAGAGT | 23607 |
rs189079822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47528927 | GCATCTTTTGCAAAT[A/G]TTTTCTCCCATTATG | 23607 |
rs189087128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47545042 | ACAAAGCAAAATCTT[C/T]TTAAACGCTTTGCCT | 23607 |
rs189120575 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | CD2AP | GRCh38.p7 | 6:47489260 | GCAACCTCCACCTCC[G/T]GGGTTCAAGCGATTC | 23607 |
rs189128152 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47594652 | TTGGAGAGTTTGGTT[C/T]TTTACAAATTCCTGG | 23607 |
rs189136004 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47577512 | ACAAGCTAAACATCC[A/G]TGAGTATGGAAATGG | 23607 |
rs189148458 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47559940 | AACCTAAGTCATGAT[A/T]TACATATTATTTTAT | 23607 |
rs189167738 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47546917 | AGAATTTTGTATCCA[A/G]CAAAACTTAGCTTCA | 23607 |
rs189180865 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47498978 | TGGCTTATTTTATTC[A/G]ATGGGGTATATTCTT | 23607 |
rs189194876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47513680 | TTTTTTGGATATTTA[A/G]GACTTTTTTTCAATT | 23607 |
rs189197681 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | CD2AP | GRCh38.p7 | 6:47518791 | CTTTTTAAAAATCAA[A/C]CACATGTCCCTTTTT | 23607 |
rs189200693 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47534845 | CACTCTGTTGTCCTG[A/G]CTGCAGTGGTGCAGT | 23607 |
rs189208554 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47483692 | AGTAGTCCAGAATTA[C/G]TGGGGTGAATGGGAT | 23607 |
rs189217096 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47523026 | TTCATAAGAAGAAAT[A/G]TTTAAGTAAAGGAAA | 23607 |
rs189222212 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47479025 | CGGGTTGAAAAGGAG[C/T]TTTGTTAAGTGGTGT | 23607 |
rs189223508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47584544 | AACTAACTGACCCCC[C/T]GATTACATTTTTGAT | 23607 |
rs189248319 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47608252 | AATATTACATATTTC[A/T]TATTTTTTAAGGCAT | 23607 |
rs189250210 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47549278 | GTCACTGTTTGCTGA[C/T]GATATGATCGTTTAC | 23607 |
rs189250752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47572443 | ATATATTACAAAACT[A/G]TCTTCTCCACTTCAG | 23607 |
rs189252308 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47620288 | ACATGCGGCTAGCCA[A/G]TTATCCCAGCACCAT | 23607 |
rs189259611 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47551533 | AAGTTTTAAAAAACC[G/T]AAGAAGATAGGTATT | 23607 |
rs189393296 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47595031 | TATTTTTGTATATAC[A/G]TCTTAAGACACATTT | 23607 |
rs189402186 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47578983 | TTCTCTTTTTTCCTC[G/T]GAGAACATTTTAACG | 23607 |
rs189433213 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | CD2AP | GRCh38.p7 | 6:47615975 | TTTTTAGTAGAGACG[C/G]GGTTTCACTGTGTTA | 23607 |
rs189434360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47504809 | TAAAAGTTATGTTTA[C/T]ATTATACTGTATTGA | 23607 |
rs189473538 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47573550 | CTGGAGTGCAGTGGC[A/G]TGATCTTGGCTCACT | 23607 |
rs189499365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47503923 | TGGGACAGTTGCCTC[A/G]CTGGTCTTCTCATTA | 23607 |
rs189500066 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47609663 | GTGAACATGCCAGTG[C/T]GCTCCAGCCTGGGCA | 23607 |
rs189503829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47539246 | TTCTGGTGTTTTATA[C/T]TGTAAACTCAGAACT | 23607 |
rs189544658 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47565765 | ACCACCTTCACTGCC[A/G]CTATCCTGGTATAAG | 23607 |
rs189549223 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47598812 | ACAGTGTGCACTGCT[C/T]GGGTGGTGGGTGCAC | 23607 |
rs189619263 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47524575 | AATCATTGTGGTATG[G/T]CTGAAAGAATGAGTA | 23607 |
rs189623373 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CD2AP | GRCh38.p7 | 6:47539572 | GTGGGCATAATATTC[C/T]AGAAATGGATATAAT | 23607 |
rs189625498 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47556961 | GTACAGGTGTTCCCA[G/T]TTCTCCACATCCTCT | 23607 |
rs189632351 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47584377 | TTTGTGATTCATTTT[G/T]AGTTAATTTTTGTGA | 23607 |
rs189647158 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47485535 | TAAAGTAAAAAGTTA[C/G/T]AGTAAGCTAAGGTTA | 23607 |
rs189651042 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47553756 | ATTAAAAATTTCATA[G/T]AAATTGAGTAATCTT | 23607 |
rs189661759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47571817 | ATTCAGTAGAGAGGC[A/G]AAGTGGGGCTAAATT | 23607 |
rs189680907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47588663 | GAAGTAGGAGTCATA[C/T]GACCTGCCACTCAGT | 23607 |
rs189719832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47606477 | AATGAAAGGTTACAG[A/G]ATCAGAAGGAAATTA | 23607 |
rs189768645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47528070 | TCAGATATCATTTCT[A/G]ATACAGATATATCAT | 23607 |
rs189772795 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47499178 | TGGAATTGGCCATTT[A/T]CCTAAAGAGTCCTGA | 23607 |
rs189777302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47523599 | TACTGTTAAAGCATT[A/G]ACTATTTTACACATA | 23607 |
rs189785343 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47590658 | TGTGCTTTTGGTATA[C/T]GTGAGGATCTTAGCA | 23607 |
rs189791865 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47556470 | CTCCTGCCTCAGCCT[A/C]CCAAGCAGTTGGGAT | 23607 |
rs189800397 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47590800 | AGATACAATGTTTTT[C/G]AATTTTCTAAAAGTG | 23607 |
rs189900120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47517913 | CGTTTAATCTAGTAG[A/G]CTTCGCTTACTAAAT | 23607 |
rs189902260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47557358 | GTCAATTTTGGCTTT[C/T]GTTGCCATTGCTTTT | 23607 |
rs189906443 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47533862 | TTGTAGACAACTACA[G/T]TAACTTCCTGCAAAG | 23607 |
rs189910698 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47575235 | TTCTCATGGTTTTTG[G/T]GGTGGTGCTCTATAG | 23607 |
rs189918943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47550072 | AATCAAGATGGATCA[A/G]GGACTTAAATCTAAG | 23607 |
rs189926952 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47591655 | GCAGTAGGACATTGA[C/G]CCTCATCTGAATTAA | 23607 |
rs189927087 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47475796 | TCCACTTCCTTATCA[C/T]TCAATTGATAAAACC | 23607 |
rs189967561 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CD2AP | GRCh38.p7 | 6:47510128 | TAATCTGGGATTAAA[A/G]ATTAACCACAGGTTA | 23607 |
rs189968643 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47611373 | TATAAAACTTTTTCT[A/G]TGGAAGAGGGGGGGA | 23607 |
rs190007274 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520220 | CATCTCTGGGGCCTC[A/G]TTATTAAAAGCTGAA | 23607 |
rs190013957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47532302 | GAGCCATGATCATGC[C/T]ACTGCACTCCAACCT | 23607 |
rs190020089 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47508569 | TTTTTTTTTTGGGAC[A/G]GAGTCTCGCTCTGTT | 23607 |
rs190022108 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47549563 | GCTGAAAGAAATAGA[C/T]GACAAAAACAAATGG | 23607 |
rs190027288 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47479732 | TAAACTACTTTGGAT[G/T]ACCTGGGGATGCAGT | 23607 |
rs190028500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47566391 | GAATGGTCTCTGATA[C/T]GTTGATGCTCAGTGA | 23607 |
rs190045233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47516939 | CTGCCAATATGAGTT[A/G]GTTGCTGGTAGTTGT | 23607 |
rs190050145 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47487416 | AACTTCTTGGCCAGG[C/T]GCGGTGGCTCACGCC | 23607 |
rs190078154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47588028 | ACATTTATTGCTTTC[C/T]GTGTGTTTGCAGTTC | 23607 |
rs190078543 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | CD2AP | GRCh38.p7 | 6:47553187 | CTGTGACTAACACAT[A/T]TTGGCTGTTAGATGA | 23607 |
rs190090556 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47610049 | CCCTTAACTCTGAAA[A/T]TTTTTTGATATGGTA | 23607 |
rs190260496 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47512377 | GGTGCATGTTATTTT[G/T]TAAATCTGTGAATAT | 23607 |
rs190262186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47491502 | GATCAGTGATATAAT[A/G]TAGAGAAGGTTAATT | 23607 |
rs190290703 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47570452 | GTTAGAAGTACCATA[A/T]AGATAAGGTTACTGT | 23607 |
rs190321061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47604194 | AGCTAAATGATTGTC[A/G]TGCCTGTTATGCCAC | 23607 |
rs190323346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47535827 | GTTTTTTCATGACCT[C/T]TGTCCATAGTAAAAT | 23607 |
rs190326702 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47568470 | GAGTAGGCTGGGCGC[A/G]GTGGCTTATGCCTGT | 23607 |
rs190328628 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47601815 | TGAAAATTTCATTAT[C/T]AGGCAACGTAATAAT | 23607 |
rs190331604 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47620865 | GGTTGTTGTTGGTGT[A/T]TAGAAGAGCTACTGA | 23607 |
rs190334040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47600132 | TGTTTAGTTTTTTTG[A/G]CTTTTTCAAAGCACT | 23607 |
rs190335450 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47545542 | CCCAGCAGGAGACCA[A/G]CCAGCACAAAAATAG | 23607 |
rs190368756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47593830 | TGACAACAGACTCTC[A/G]TGTATTGTATGTAAA | 23607 |
rs190500814 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47489852 | AGTTAAACAGAGCAA[G/T]TAATATGACCTTCAG | 23607 |
rs190502679 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CD2AP | GRCh38.p7 | 6:47495438 | ACTAACCCTGCTGAT[A/G]CCTTGATTTTGCCCT | 23607 |
rs190542950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47560286 | AAAGTTAGTCTCTTA[C/T]GTAACTACAGTACAG | 23607 |
rs190544466 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47565164 | TAAAAGTTTTAAGAA[A/T]GCCACCATTATGTTT | 23607 |
rs190556931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47546735 | CATTGTCATCAGGTT[A/G]TCTAAAGTTAAGATG | 23607 |
rs190566173 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CD2AP | GRCh38.p7 | 6:47561999 | TGGTCTCAATGACCT[C/T]GTGATCCGCCCACCT | 23607 |
rs190574488 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47491788 | TTTTAAGCTTGATCT[G/T]CAGATATCCTTTTTG | 23607 |
rs190574903 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47531790 | TATAAGAATCCTTTT[C/T]GGCCGGGCGTGGTGG | 23607 |
rs190579975 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CD2AP | GRCh38.p7 | 6:47529275 | GTTCAGTGTCGTTTT[A/G]TTGTAATGTTGATGA | 23607 |
rs190586048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47587142 | TGTTCCCATAGTTGA[A/G]AGAGGGAGCATTTTC | 23607 |
rs190588967 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47513580 | TGGTGTTTAAGACTG[A/C]ACATACAGTATTATA | 23607 |
rs190594966 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47529996 | TGCTCATATGCTATG[A/C]TTTCCTGTTAAGACA | 23607 |
rs190606023 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47617540 | TTTGATTTCCTGTTG[C/T]TGTTGATAATTTCTG | 23607 |
rs190615285 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47500840 | CAACCTCCGCCTCCC[A/G]GATTCACGCCATTTC | 23607 |
rs190621588 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | CD2AP | GRCh38.p7 | 6:47561051 | ATCAGTCTATTACCA[A/G]TATTATTTATTTTGA | 23607 |
rs190621895 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47580264 | TTATCAATTATTCTT[A/C]ATTTGTAAAAACCAA | 23607 |
rs190623839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47537613 | AGTTGAAAGTATGCT[A/G]CAGACATAATACATT | 23607 |
rs190629460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47595705 | ATTAAAATATAACTT[C/T]AAAATAAGTAAAACA | 23607 |
rs190794913 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47487185 | CCATTCTTAACAAAC[A/G]TATTTTAGGAAGCAG | 23607 |
rs190820042 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47515104 | AGGTAGAAAGTTATA[A/G]GAGTACTGAGTGCAT | 23607 |
rs190840846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47579645 | GAGTTATAGTAAAAC[A/G]AAATAATGTTTCAGT | 23607 |
rs190861196 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | CD2AP | GRCh38.p7 | 6:47545982 | TCACACTAGCTCACC[A/C]GCAAGGTATCCAAAC | 23607 |
rs190862649 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47525973 | GACTCTTTTTTACTA[C/T]ATCTCCTGAAGTTAT | 23607 |
rs190867769 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47617994 | CAAACAATTACCTTC[A/G]TTAAATTGATACTAG | 23607 |
rs190868590 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521069 | TTTATTTTTTACATA[G/T]GTAAGGTCCAGAGCT | 23607 |
rs190870582 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47616813 | TTGCATCTTAGGTTA[G/T]GTTTACTGATGCCAA | 23607 |
rs190876146 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47596513 | TTGAGTGGAGAACAT[G/T]TGGTATTTGTCTTTC | 23607 |
rs190891509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47586029 | TCTGATTAAAGATTG[C/T]CAGGCATAGAAAGAG | 23607 |
rs190926331 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47621211 | TTATTACATTGAGGT[A/G]TATCCCTTGTATGCC | 23607 |
rs190940828 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520419 | TGTTGACAGTTGTCG[A/G]GAGGGGCTCCCCACT | 23607 |
rs190950371 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47537155 | AAGCTAGTTGAAACA[A/G]TGCCAGTCTACACAT | 23607 |
rs190955250 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CD2AP | GRCh38.p7 | 6:47553481 | CTTCCCAGCTAGATG[A/G]GACTACAGGTGTGCA | 23607 |
rs190962305 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47481250 | TTCTAAGGGCAGAAT[G/T]TCTCTTTAATAATTT | 23607 |
rs190980488 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47500631 | ATTTTCATCTTTTTT[C/T]TCCTCCACGTTAATT | 23607 |
rs191017310 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47571683 | ACTGAACATGAGCAG[A/C]TTGTGAAGAAAGAGC | 23607 |
rs191107478 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47508108 | CCACTTAAATTACCA[A/G]CTGCATTAGTCCCTA | 23607 |
rs191124353 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47539841 | ATTTTTGTACAATTA[A/T]TTTTTTTGTAGAACT | 23607 |
rs191133253 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47600422 | TAAAATATGCTATTA[C/T]ATTTCAGGGTTTTTC | 23607 |
rs191136417 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CD2AP | GRCh38.p7 | 6:47573399 | TGGATTGAATCATAT[A/G]GCTTTAAAAAATAAT | 23607 |
rs191155837 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47567306 | AGGGTATTCCAAAAT[C/T]TGAAATTTAAAAGTC | 23607 |
rs191159955 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47540768 | TTCATGAAAAAGAAA[A/C]CACATTTTAAAAAAG | 23607 |
rs191170481 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47612108 | GTTAACTTGCCTTGT[A/C]TTGTGATGTGTTGAT | 23607 |
rs191173085 | snp | A/C | 0 | 0 | intron-variant | CD2AP | GRCh38.p7 | 6:47590306 | AATATGAGTCAGTCT[A/C]AGCTTAAATGAATTT | 23607 |
rs191240390 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47530698 | AAGACAGTCTCTCTT[G/T]TTAACATTTGTATGC | 23607 |
rs191244449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47547391 | CTATGCTTATATCAG[A/G]CAAAACAAACTTTAA | 23607 |
rs191271162 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47513897 | AATTTTTTTTTGGGG[C/G]GGGGGCTAGCCTTAC | 23607 |
rs191273282 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47492946 | ATACATTTATAACTA[A/G]TGTTAAATTCAGCTT | 23607 |
rs191336662 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47526274 | TGTTTCTAGTAGTAA[A/G]GGATTGTAGCTCGGA | 23607 |
rs191350871 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47496000 | TTTTTAATTTCCTAT[A/G]TGATGTTACTGTTTT | 23607 |
rs191356336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47529547 | CCTGAACTGGAATAG[A/G]TGCATAAATAGTTAT | 23607 |
rs191382971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47576455 | GGGTAACTGTAAATG[A/G]AAACTTTGTTTAACA | 23607 |
rs191383124 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47535028 | TCTTGAACTCCCGGG[A/C]TCAAGTGATTTGCCC | 23607 |
rs191387214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47551745 | CTGGAAAGATTCAAT[A/G]GTGGGGTGTCCTGGA | 23607 |
rs191397279 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | CD2AP | GRCh38.p7 | 6:47568739 | ACAGAGTGAGACTCC[G/T]TCTCAAATAAATAAA | 23607 |
rs191404839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47557854 | TAGTTTTTTTCTAAT[C/T]CTGTGAAGAAAGTCA | 23607 |
rs191408135 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47532596 | GTTTATGGATTTCCT[A/G]TTTTGTTTCATTTAT | 23607 |
rs191410480 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47613146 | CTCCACTGAAGTCTT[C/T]AATCCTCAAAGTCAT | 23607 |
rs191418610 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47594208 | GGTGGTGGTTGCGTA[A/G]CATCGTGAATGTACT | 23607 |
rs191430401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47566599 | CTATCGACCCATCCT[C/T]TCAATTCTCCCTTCC | 23607 |
rs191580009 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47480566 | ACTGAGCACATTACT[G/T]CTCTGTGCTTCAGTT | 23607 |
rs191594572 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47481756 | TTGGAGAAAATATTT[A/T]AAAAATTTTTATTTA | 23607 |
rs191670434 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47549726 | TCTAAAATTCATATG[G/T]AACCAAAAAGAGCCT | 23607 |
rs191695660 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47612645 | TGCTATACTACTTCA[G/T]TTGGACATACACACA | 23607 |
rs191725465 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47627699 | GAGTTACTGAGTTAA[A/T]CAAAGAATGAAATTT | 23607 |
rs191737305 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47528486 | AGCCAGTTCATTTAT[G/T]ATATATGGAACTTAT | 23607 |
rs191745183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47568064 | GTGATAGCACAAAGA[A/G]CAGGACCTAGTGATA | 23607 |
rs191768133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47586364 | ATAGAACCATTAAAA[A/G]TGTATAGAAAAAAAG | 23607 |
rs191771777 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47534264 | ATCAGATAAGGGTTT[C/G]AGTCTGTCTTATGAC | 23607 |
rs191777396 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47488927 | TTTTTGTTTTTTGTA[C/T]GTGTTTATTTTGGGT | 23607 |
rs191779070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47510136 | GATTAAAAATTAACC[A/G]CAGGTTACTAGATTA | 23607 |
rs191780425 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47550602 | TGGGAATGTAAACTA[A/G]TACAGCCACTATGGA | 23607 |
rs191799231 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47621682 | TGGTCCTGGGCTTTT[C/T]TTTGTTGGTAATTTT | 23607 |
rs191802391 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47600645 | TCATTGAAATTTATT[C/T]GGTATGTTTTATATG | 23607 |
rs191879858 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | CD2AP | GRCh38.p7 | 6:47541379 | TCCGCCTGCCTCGGC[C/T]TCCCAAAGTGCTGGG | 23607 |
rs191894051 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47499739 | AGTTAAGAGTTTTGT[C/T]GTTGTTGTTGTTGTT | 23607 |
rs191903307 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CD2AP | GRCh38.p7 | 6:47513818 | TATACTAGATGTTGT[C/T]TGATTTCTCTCTCAA | 23607 |
rs191915147 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47487854 | GCAGAAAATTAGGAG[A/C]CTGCTATGTATCCAC | 23607 |
rs191920077 | snp | C/T | | | utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47477807 | TGTCTGGGTCCCCAC[C/T]TTAGTCTACGGTGTC | 23607 |
rs191924128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47605971 | AAATGTATCAGGTAA[A/G]GAGGATTTTTTTTTT | 23607 |
rs191924477 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47509210 | GACACACAATATTTA[G/T]TAAATTTGCTGTCTG | 23607 |
rs191928407 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47527311 | CCTTCCCACCTCCCA[C/T]GGATCAACTGAAAGT | 23607 |
rs191953999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47546958 | AAACATACAGTCTTT[C/T]TCAGACAAACAAATG | 23607 |
rs191961100 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47581170 | TTAAACTGTTTTAGA[A/C]AACTTAATATATTGA | 23607 |
rs192025449 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47607225 | TGGACACTTAGGTTG[A/G]TTCCAATTCTTGGCT | 23607 |
rs192039583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47622084 | AGCTAGGAGGAATAT[A/G]GCTGCCTATGCTGAA | 23607 |
rs192106379 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47496634 | AAAGTAATTCCTGCA[C/T]GTGATATACAAATAT | 23607 |
rs192150188 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47503928 | CAGTTGCCTCGCTGG[C/T]CTTCTCATTATATTT | 23607 |
rs192187962 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47597237 | TGCTGCTAGGCATCA[A/T]GGAGAAAGCAGCAGA | 23607 |
rs192188295 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47482598 | TTAGCCAGGATGGTC[C/T]CGATCTCCTGACCTT | 23607 |
rs192191788 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47491974 | GTAATGTACTTTACT[G/T]TCTTTTACCTGTTTT | 23607 |
rs192202406 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47564383 | TTACAACTTAAAGTT[C/T]GTATGGGACCACCAG | 23607 |
rs192211656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47539038 | TATGATCATGAGAAA[C/T]AATATTGGTCTAGGC | 23607 |
rs192249079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47588366 | ATTGGTTCTCTAATG[C/T]GTTACACAATAGGTA | 23607 |
rs192266550 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47530494 | TTTCAATCAGAATTA[G/T]AAATTGATAGATTTT | 23607 |
rs192266748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47564836 | GCTGTTAGAAAAATT[A/G]TAGTAGAATGTACAT | 23607 |
rs192279940 | snp | A/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625244 | CTTCAGTGTGAGGTT[A/T]CCTATTTTGACAAGT | 23607 |
rs192284330 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | CD2AP | GRCh38.p7 | 6:47597429 | GAGGACCCAGAGGCT[A/T]GATGAGAGAATAAAA | 23607 |
rs192293436 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47583784 | GTAAATACCAAGGAG[A/C]GGGATTACCTGATAA | 23607 |
rs192296837 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47531404 | TTATTACTAATGAAA[C/T]GTGTACACCTTTTGG | 23607 |
rs192305647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47547978 | ATTCTTCTTACTGAA[C/T]GACAATAGTGACACA | 23607 |
rs192318149 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47619230 | CTCGCCCCCTTCCCA[C/G]TCTTCAACTCAAGTC | 23607 |
rs192373863 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47488651 | GATTATAAGAATTTA[C/G]TGAGGCAGGAGGATT | 23607 |
rs192448330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47527727 | ACGTTGAGTGATACC[C/T]GCAGATTAGTTGTTT | 23607 |
rs192452960 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47555973 | TTGAAATTAAGTAGG[A/G]AAACATAAAGTTGGT | 23607 |
rs192463808 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47572724 | CTGTAGGTCCCTGGG[A/G]AAGTCATTAATATCC | 23607 |
rs192464808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47559021 | GTTATTGGTCTATTC[A/G]GGGATTTGGCTTCTT | 23607 |
rs192474406 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47622624 | TTTCTCCAGTGCGGG[G/T]TGTGTGTTCGGGAGA | 23607 |
rs192477682 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47503672 | CTTGTATATGGTTGT[A/G]TGTATCTACCTGATT | 23607 |
rs192478380 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47483277 | TCTGGATGGAGGTCT[A/C/G]TATGTGCCTACAGTC | 23607 |
rs192480553 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47517014 | TGGGGCCTGGTGGGA[A/G]GTGATTGACCCATGG | 23607 |
rs192491028 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47522625 | AAGAAGAAAACAAAA[A/G]TTACCCAGTAAGTTT | 23607 |
rs192496602 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47587314 | TCAGAGATGTGGGGC[G/T]CAGAAAAGAGCTACT | 23607 |
rs192516322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47483982 | GGCAGAAGAAACTTG[A/G]AAGTATTAGTAATTA | 23607 |
rs192519294 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47589645 | AATCATAAGATCAAG[A/G]TAGAGGGGAAGAGGA | 23607 |
rs192539108 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47523263 | ATTAAGGGAGAAAAC[C/G]TTGCAGATATTGGAA | 23607 |
rs192593327 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47581950 | TAGAAGTGTAATTGT[C/T]TCTGTGCTTTAAAAC | 23607 |
rs192623727 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47556164 | TGCACCTATCAACCC[C/G]TCATCTACATTAGGT | 23607 |
rs192630819 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CD2AP | GRCh38.p7 | 6:47618762 | ACAAGAGTCAAATTG[C/T]TTCTCTTTTGGATAA | 23607 |
rs192642113 | snp | G/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47477166 | TTTCTCTCGATCAAG[G/T]AACAACTCAAATTAT | 23607 |
rs192679464 | snp | A/G | 0.000197984 | 0.0099475 | missense | CD2AP | GRCh38.p7 | 6:47544618 | TAGAGACCAAGAAGC[A/G]TCAGTGTAAAGTTCT | 23607 |
rs192697628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47518455 | ATAATAATTTAGTAT[A/G]ATTAATAATGATTGG | 23607 |
rs192707137 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47613961 | TAAACCACATGAACC[A/T]GCCTCTGCTACCTTC | 23607 |
rs192727786 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47577274 | AATAAGTGCTCAGAA[C/T]GTTCTCTTTTTGAGC | 23607 |
rs192747779 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47509604 | ATATTTAGAGCAAGG[C/T]CACTTCATTTTTTGT | 23607 |
rs192783667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47542688 | AAGTAAATTTATACT[A/G]TCTTCATTACCTAGT | 23607 |
rs192796108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47601898 | TTATTTACTAGTTGA[C/T]TGCTGATAGTAAGTT | 23607 |
rs192808790 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47498490 | TAGGATTATTTTCTT[C/G]TATTATTTCATGGTT | 23607 |
rs192847980 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47568267 | TGGATCATTGAAAAT[C/T]ACCAACTTTTACTAC | 23607 |
rs192851990 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47600958 | ATGGAGTCCCTTTGG[A/G]AATTGAAGGAGTAAA | 23607 |
rs192872094 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47497689 | AAAGTGTTGGGATTA[C/T]AGGTGTGAGCTGCAA | 23607 |
rs192901070 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47559775 | GAATGATTCATGCAG[C/G]TTTTTCCCACCTAAT | 23607 |
rs192917018 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47594551 | TTTTTCTTGGTATGT[A/T]ATATAAAACATCTCT | 23607 |
rs192935034 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47494058 | TGTTGTATCTGAGTC[A/G]GGTTCAGATGCTTGC | 23607 |
rs192935921 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521467 | TGAGGCAGGAGAAGT[C/G]CTTGAACCCGGGAGG | 23607 |
rs192953372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47589230 | GTATTAAGTGTTTAG[C/T]TGGAAGGTGCTATTC | 23607 |
rs192969470 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47554494 | TTTAATCCACTTAAA[A/G]TATATTTTCTTCATT | 23607 |
rs193015188 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CD2AP | GRCh38.p7 | 6:47518703 | AGAAACTGCAAAACT[A/G]TATTCTGAAGTGATT | 23607 |
rs193037910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47586917 | GTTAAACAAGAGAAG[A/G]CATAACAAAGGAAAT | 23607 |
rs193050645 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47551275 | ATTTCACAGTTGAAG[A/G]TCATGTTTTCAACAT | 23607 |
rs193098419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47584383 | ATTCATTTTGAGTTA[A/G]TTTTTGTGAAAGTTG | 23607 |
rs193167351 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47501935 | AACTTAGTAGTTTAG[A/T]ACTATATATATTTAT | 23607 |
rs193172055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47537651 | ATCACATTATCTTTT[C/T]CTTCATGATAGTGAT | 23607 |
rs193186329 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47514934 | GCACGCACCTGCAAT[C/T]CCAGCTACTCGGGAG | 23607 |
rs193189425 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47572275 | CTGCGCCCGGATCCA[C/G]TGCGATGGTGTACAA | 23607 |
rs193264594 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47598414 | GGTATCTACCCAGAG[A/G]AAAATAAGTTATTAT | 23607 |
rs199539474 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47587432 | TAGGTGATTAAACTC[-/T]CACTTTCTACTTTCT | 23607 |
rs199547303 | snp | A/G | 5.04817e-05 | 0.00502377 | missense | CD2AP | GRCh38.p7 | 6:47599323 | GGGGAAGTTTCTAGC[A/G]TTTCATCAAAATTTG | 23607 |
rs199562171 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47478215 | AGGAGGAGGAGCGGA[C/T]GTCGGCTTCTCCCCG | 23607 |
rs199576264 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47587431 | ATAGGTGATTAAACT[C/T]TCACTTTCTACTTTC | 23607 |
rs199599552 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47568743 | AGTGAGACTCCGTCT[C/T]AAATAAATAAATAAA | 23607 |
rs199622885 | snp | A/G | 3.31076e-05 | 0.0040685 | missense | CD2AP | GRCh38.p7 | 6:47576587 | ACAAAAACAGATACC[A/G]AAGGTAAAATTAAAG | 23607 |
rs199681910 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47536240 | GATTTTTTTTTTTTT[A/C]TTACTGTTTGGATCA | 23607 |
rs199689963 | in-del | -/TT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47610947 | ATAAAATATTTCTGA[-/TT]TTTATATATATATAT | 23607 |
rs199709906 | in-del | -/AT | 0.0232847 | 0.105357 | intron-variant | CD2AP | GRCh38.p7 | 6:47551278 | TCACAGTTGAAGGTC[-/AT]GTTTTCAACATGTAT | 23607 |
rs199759400 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47512166 | CGTCTGAAAAAAAAA[-/T]ATATATATAAAATAA | 23607 |
rs199760461 | snp | A/G | 0.330249 | 0.23677 | intron-variant | CD2AP | GRCh38.p7 | 6:47551188 | AACCTATGGAAATAA[A/G]AAAAAGAAAAAAAAA | 23607 |
rs199761911 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47610971 | TATATATATATATGT[A/T]TTTTTTTTTTTTTTT | 23607 |
rs199770308 | in-del | -/AAA | 0.0178098 | 0.0926698 | intron-variant | CD2AP | GRCh38.p7 | 6:47595706 | TTAAAATATAACTTT[-/AAA]ATAAGTAAAACAGTG | 23607 |
rs199784592 | in-del | -/A | 0.0174175 | 0.0916809 | intron-variant | CD2AP | GRCh38.p7 | 6:47612670 | ACACAATGGACTACT[-/A]ATTCAGTCACAAAAA | 23607 |
rs199881689 | in-del | -/G | 0.0232847 | 0.105357 | intron-variant | CD2AP | GRCh38.p7 | 6:47509321 | ATAATGAAGAAGTTT[-/G]GAAATATTGCAAGAA | 23607 |
rs199885174 | in-del | -/A | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47522026 | GCCTCAAAAAAAAAA[-/A]GAAAGAAAGATAACC | 23607 |
rs199897205 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47594974 | TTTTTCAAAGACCAA[A/C]TAAATTTTGAAAATT | 23607 |
rs199920707 | in-del | -/GA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47486428 | ATTAGAAAAATAAAC[-/GA]GAGAGAGAGTATAGG | 23607 |
rs199983935 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497331 | CTTTCCTTTCCTTTC[A/C]TTTCCCTTCCCTTCC | 23607 |
rs199995766 | snp | A/G | 1.70566e-05 | 0.00292027 | intron-variant | CD2AP | GRCh38.p7 | 6:47579371 | TGTCTTAATTATTCT[A/G]TTTTGCTTTTTAGGA | 23607 |
rs200023127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47554811 | TTTAAATAAACTTTA[C/T]ATAGCATCTAGTGTT | 23607 |
rs200024855 | snp | A/G | 6.67379e-05 | 0.0057762 | missense | CD2AP | GRCh38.p7 | 6:47609141 | TCTGTGTACCTTTCA[A/G]CACCTTCCAGTGCTT | 23607 |
rs200038619 | in-del | -/AC | | | intron-variant | CD2AP | GRCh38.p7 | 6:47589518 | TACACATACGTATGT[-/AC]ACACATATATACACA | 23607 |
rs200064899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47533260 | TGTAAAATATTTACT[A/G]TCTGGCACTTTATAG | 23607 |
rs200073791 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47607128 | TCCATGTTGCAAATG[A/G]CAGGATCTCATTCTT | 23607 |
rs200080006 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47595631 | ACTAATCGGAAGCTT[A/G]TTAGTGGTTTTCCTC | 23607 |
rs200158608 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47607137 | CAAATGACAGGATCT[C/T]ATTCTTTTTTGTGAC | 23607 |
rs200178991 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47561473 | CCTATCAAGGCAAAC[-/T]TTTTTTTTTTTTAAG | 23607 |
rs200185463 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47603017 | ATATTTGGTAGTTGA[C/T]CTATTTTTTAAAAAT | 23607 |
rs200187684 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497339 | TCCTTTCCTTTCCCT[C/T]CCCTTCCCTCCCCTT | 23607 |
rs200203288 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47515848 | TTTGATGGAAGTAAA[-/T]TTTTTTTTTTTAAAC | 23607 |
rs200209388 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47615787 | TTTTAATTTTAATTT[A/T]ATTTAATTTATTTAT | 23607 |
rs200226751 | snp | A/G | 3.41565e-05 | 0.00413244 | missense | CD2AP | GRCh38.p7 | 6:47624186 | TGTTTTTTGTTTTAG[A/G]TGGAAATAGAGAAGC | 23607 |
rs200255765 | snp | A/G | 1.79606e-05 | 0.00299666 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47612533 | AATGAGAAGTAATCT[A/G]GAGGTAATTAATTTC | 23607 |
rs200257141 | in-del | -/A | 0.00953873 | 0.0683987 | intron-variant | CD2AP | GRCh38.p7 | 6:47547871 | ATCAACTCCAAAAGG[-/A]GCCTTGAAAACCATG | 23607 |
rs200351883 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47534548 | CCCATCTCTACTAAA[C/T]ATACAAATTAGCCGG | 23607 |
rs200388357 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47499307 | CTAGGGTGTATGTGC[A/G]TGTGTGTGTGTGTGT | 23607 |
rs200389369 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47570616 | CTCTCTCTGTCACTT[A/T]ATGGTTCTCAGTGAT | 23607 |
rs200397134 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47570545 | TCCTTATCCTCTTTT[C/T]TTCTTTCCAGTGGCT | 23607 |
rs200404923 | snp | A/C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47597791 | AGTCCCAAACTCCAC[A/C/G]ACACCAGTACCTGCC | 23607 |
rs200440845 | snp | C/T | 0.00199806 | 0.0315443 | missense | CD2AP | GRCh38.p7 | 6:47533642 | AGGATGACAGTTTGC[C/T]CATCAAACGGGAAAG | 23607 |
rs200463256 | in-del | -/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47610987 | TTTTTTTTTTTTTTT[-/G]AATATAAAACATTTT | 23607 |
rs200477829 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47610967 | TATATATATATATAT[A/G]TGTATTTTTTTTTTT | 23607 |
rs200495170 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47491277 | TGTGTGTGTATGTGT[A/G]TGTGTGTGTGTGTGT | 23607 |
rs200506346 | snp | A/C/T | 0.000382037 | 0.0138158 | intron-variant | CD2AP | GRCh38.p7 | 6:47607912 | ATGTCTCTTGACTTC[A/C/T]AAAAAATCATTTAGC | 23607 |
rs200545750 | snp | A/G | 5.11941e-05 | 0.00505909 | intron-variant | CD2AP | GRCh38.p7 | 6:47579508 | AGCTTTTGTTTTTCA[A/G]TGATGATAATACTTG | 23607 |
rs200545880 | in-del | -/CT | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624677 | CATAAGGGATATAAA[-/CT]CTGTGTGTGTGTGTG | 23607 |
rs200560036 | in-del | -/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47570538 | TCCTTGCTCCTTATC[-/C]TCTTTTCTTCTTTCC | 23607 |
rs200560648 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47610972 | ATATATATATATGTA[A/T]TTTTTTTTTTTTTTG | 23607 |
rs200569099 | in-del | -/CA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47587433 | AGGTGATTAAACTCT[-/CA]CTTTCTACTTTCTGT | 23607 |
rs200574128 | in-del | -/TGCAAATGACAGGATCTC | | | intron-variant | CD2AP | GRCh38.p7 | 6:47607120 | TAGTTCCATCCATGT[-/TGCAAATGACAGGATCTC]ATTCTTTTTTGTGAC | 23607 |
rs200598584 | snp | A/T | 0.00118642 | 0.024327 | intron-variant | CD2AP | GRCh38.p7 | 6:47554785 | GACTATTTTTTAAAA[A/T]TTTTAATTGATTTAA | 23607 |
rs200636554 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | CD2AP | GRCh38.p7 | 6:47586935 | TAACAAAGGAAATGA[-/T]TCTAAGTATTTTCAG | 23607 |
rs200639515 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47510970 | CCCAGCTACTCAGGA[A/G]GCTGAGGTGGGAGAA | 23607 |
rs200644975 | in-del | -/TG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47610968 | ATATATATATATATA[-/TG]TATTTTTTTTTTTTT | 23607 |
rs200678689 | in-del | -/TGTGTG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47491272 | ATATGTGTGTGTGTA[-/TGTGTG]TGTGTGTGTGTGTGT | 23607 |
rs200729230 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47570153 | TTTCTTTTTTTTTTT[A/T]AAGCTTTCAGTGCAG | 23607 |
rs200745225 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47513893 | AAAAATTTTTTTTTG[-/T]GGGGGGGGGCTAGCC | 23607 |
rs200752323 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47556505 | GGCATGTGCCACCAC[A/G]CCCAGCTAATTTTTT | 23607 |
rs200757404 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CD2AP | GRCh38.p7 | 6:47493367 | GTGTTTTTTTTTTTT[A/G]CAATGCTTTAAATAT | 23607 |
rs200757481 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47606643 | CTGAAATATTCAGTG[G/T]TTTTTTTCTTTTCTT | 23607 |
rs200795452 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47580462 | AAAACCAAAACAAAA[A/C]AAACAAAAAAAAAAA | 23607 |
rs200798500 | snp | A/G | 6.5912e-05 | 0.00574035 | missense | CD2AP | GRCh38.p7 | 6:47595959 | GCCAGTAATTTACTG[A/G]GATCTTCTGGAACAG | 23607 |
rs200805546 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47482370 | CGGAAGTTTGCTTTG[-/T]TTTTTTTGTCTTTTT | 23607 |
rs200806448 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47587429 | AGATAGGTGATTAAA[A/C]TCTCACTTTCTACTT | 23607 |
rs200813397 | in-del | -/TAG | 0.00914312 | 0.0669923 | intron-variant | CD2AP | GRCh38.p7 | 6:47513003 | TAGCTTATAGGTAAT[-/TAG]TAGAGAGAAATGATG | 23607 |
rs200858341 | in-del | -/T | 0.00835141 | 0.0640778 | intron-variant | CD2AP | GRCh38.p7 | 6:47488882 | GCAACTGAGTGAGTC[-/T]TTTCTTAAAAAAAAA | 23607 |
rs200863727 | in-del | -/T | 0.0256215 | 0.110247 | intron-variant | CD2AP | GRCh38.p7 | 6:47540561 | TCCTTTGATTAAATC[-/T]TTTTTTTTTCATTTT | 23607 |
rs200865789 | in-del | -/AA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47615795 | TAATTTAATTTAATT[-/AA]TATTTATTTATTTAT | 23607 |
rs200869952 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47527113 | TAAAAGACTCCCCCC[C/T]GATTGAAAAATATTC | 23607 |
rs200919967 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47551194 | TGGAAATAAAAAAAA[A/G]AAAAAAAAATTTAAA | 23607 |
rs200965914 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47506356 | CCTCACATCCCAGAC[A/G]ATGGGCGGCCAGGCA | 23607 |
rs200966093 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47570547 | CTTATCCTCTTTTCT[C/T]CTTTCCAGTGGCTGT | 23607 |
rs200971908 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47567098 | AGTTTTTTTTTTTTT[A/T]ACTTTACTATGCTGT | 23607 |
rs200993256 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497332 | TTTCCTTTCCTTTCC[C/T]TTCCCTTCCCTTCCC | 23607 |
rs200997555 | snp | A/G | 0.00597247 | 0.0543191 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626456 | TCATGAATTTTTTTT[A/G]TACGTGTGAGTATAA | 23607 |
rs200998882 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47495827 | CCACAATTTTTGGCG[-/T]TTTTATGCTTTTTCT | 23607 |
rs201073540 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47607135 | TGCAAATGACAGGAT[C/T]TCATTCTTTTTTGTG | 23607 |
rs201094245 | in-del | -/TTTTTTTTT | 0.493881 | 0.054972 | intron-variant | CD2AP | GRCh38.p7 | 6:47489165 | ACTGCACTCAACTAG[-/TTTTTTTTT]TTTTTTTTTTTTTTG | 23607 |
rs201146918 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47513542 | AGTGGTATTTTAGTG[-/T]TTTTTTTTTCTCCCA | 23607 |
rs201150299 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47589567 | ACACACACACACACA[C/T]ATATATATATATATT | 23607 |
rs201151056 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47557442 | TAGGTTTTCTTCTAG[A/G]GTTTTTATGGTTTTA | 23607 |
rs201182102 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47513160 | TTTTTTTTTTTTTTT[C/T]TTCTTTTAAAGTAAC | 23607 |
rs201196580 | in-del | -/A | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47584909 | TATTTTTTTACTATT[-/A]AAAAAAATCATGTCA | 23607 |
rs201217393 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47575507 | TGATCCAGGAATTGA[A/T]AAAATAGGGAGCACA | 23607 |
rs201224655 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47611084 | GTTTTTTTTTTTTTA[A/T]TATCTAAAAAACTTG | 23607 |
rs201232118 | snp | C/T | 3.29696e-05 | 0.00406001 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47574164 | GAAAATTCGAGGAAT[C/T]GGATTTGGAGACATT | 23607 |
rs201251439 | snp | A/C | 0.00199808 | 0.0315444 | missense | CD2AP | GRCh38.p7 | 6:47607971 | GTTACCAAAAGAAGA[A/C]GACAGTGCCAACCTG | 23607 |
rs201291952 | in-del | -/T | 0.308661 | 0.24302 | intron-variant | CD2AP | GRCh38.p7 | 6:47605977 | ATCAGGTAAAGAGGA[-/T]TTTTTTTTTTCTTTT | 23607 |
rs201314621 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47619377 | AGTCTCCAATTTCAT[C/G]CAGGTCACTGCAGAT | 23607 |
rs201326039 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47507596 | GATTACAGGCTCCCA[C/T]CACCACGCCCAGCTA | 23607 |
rs201329353 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47577933 | TATATAATTTTTTTT[A/T]AAAATAAGTTTTATT | 23607 |
rs201378568 | in-del | -/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47607137 | CAAATGACAGGATCT[-/C]ATTCTTTTTTGTGAC | 23607 |
rs201405459 | in-del | -/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47513893 | AAAAAATTTTTTTTT[-/G]GGGGGGGGGCTAGCC | 23607 |
rs201416726 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47491279 | TGTGTGTATGTGTGT[A/G]TGTGTGTGTGTGTGT | 23607 |
rs201437337 | in-del | -/AT | 0.0391387 | 0.134304 | intron-variant | CD2AP | GRCh38.p7 | 6:47550733 | GATAGTTGCACACAC[-/AT]GTTTATAGCAGCACA | 23607 |
rs201466682 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47609532 | AAAAAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAG | 23607 |
rs201472431 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47543186 | AAGAAAAAGAAAAAA[A/G]AAAAAAAAGAAAAAG | 23607 |
rs201490626 | in-del | -/AT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497144 | TATTATGACCATGTC[-/AT]GTGTTTTTTTTTTAC | 23607 |
rs201498860 | in-del | -/ACAT | 0.0103295 | 0.0711199 | intron-variant | CD2AP | GRCh38.p7 | 6:47589522 | CATACGTATGTACAC[-/ACAT]ATATACACATATGTA | 23607 |
rs201510605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47539672 | CATTGGTAAATGAGA[C/T]AGTGAGTGTTAATGC | 23607 |
rs201529726 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47555894 | GTTGTGAGCTATTAG[-/T]TTTTTTTTTCTTGCT | 23607 |
rs201551523 | in-del | -/A | 0.00914312 | 0.0669923 | intron-variant | CD2AP | GRCh38.p7 | 6:47489587 | TTTCAGTTGATACTT[-/A]AGTTACTAGCATTTA | 23607 |
rs201628924 | in-del | -/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47513157 | CTTTTTTTTTTTTTT[-/C]TTCTTCTTTTAAAGT | 23607 |
rs201648954 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CD2AP | GRCh38.p7 | 6:47532004 | CTTGAACCCAGGAGG[C/T]GGAGGTTGCAGTGAC | 23607 |
rs201662642 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47618992 | TATAATGTTAACATT[A/G]TACAGTATTATAATG | 23607 |
rs201663973 | in-del | -/GTA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47610969 | TATATATATATATAT[-/GTA]TTTTTTTTTTTTTTT | 23607 |
rs201673149 | snp | C/G | 0.000264053 | 0.0114872 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47595919 | TCCACAAGTCCCACC[C/G]AAGAAACCTACTCCA | 23607 |
rs201705857 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47564866 | TTATATAAGTGTTTT[C/T]TTTTTTGCTTTCATT | 23607 |
rs201727632 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47554815 | AATAAACTTTATATA[A/G]CATCTAGTGTTTTAT | 23607 |
rs201741408 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47570544 | CTCCTTATCCTCTTT[C/T]CTTCTTTCCAGTGGC | 23607 |
rs201742003 | in-del | -/TCCCCT | 0.314544 | 0.241524 | intron-variant | CD2AP | GRCh38.p7 | 6:47497348 | TTCCCTTCCCTTCCC[-/TCCCCT]TCCCCTTCCCCTTCC | 23607 |
rs201755513 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47617214 | AAGTGATCCTCCCAC[C/T]TTGGCCTCCCAAAGT | 23607 |
rs201792454 | snp | C/T | 1.68066e-05 | 0.00289879 | intron-variant | CD2AP | GRCh38.p7 | 6:47595812 | TTGGAAATAGAAAAA[C/T]CTAAATAATTTTGAT | 23607 |
rs201842906 | snp | G/T | 0.00166089 | 0.0287696 | intron-variant | CD2AP | GRCh38.p7 | 6:47606289 | TTCTGTGAGTTCATC[G/T]AATTGTCGTAAACTA | 23607 |
rs201867145 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47611387 | TATGGAAGAGGGGGG[C/T]AATAGGATTAAGGAA | 23607 |
rs201888913 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497327 | TTTCCTTTCCTTTCC[C/T]TTCCTTTCCCTTCCC | 23607 |
rs201892753 | snp | C/T | 1.67818e-05 | 0.00289665 | missense | CD2AP | GRCh38.p7 | 6:47624217 | TGAAAAAAGCTGTCC[C/T]GTCTTCTTGAGTGGT | 23607 |
rs201892841 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47589449 | ACATACACACACACA[A/C]ATATATATACATATA | 23607 |
rs201953702 | in-del | -/TAAT | 0.00717837 | 0.0594782 | intron-variant | CD2AP | GRCh38.p7 | 6:47587561 | TGTGTCCCAGAATGG[-/TAAT]AATATTACCACTTTG | 23607 |
rs201965255 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47564869 | TATAAGTGTTTTCTT[A/G]TTTGCTTTCATTATT | 23607 |
rs201976901 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47585298 | ACAGAGCAAGACTCC[A/G]TCTCAAAAAAAAAAA | 23607 |
rs201991686 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47587430 | GATAGGTGATTAAAC[A/T]CTCACTTTCTACTTT | 23607 |
rs202056941 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47556400 | CATTCTTTTTTTTTT[A/T]AATTTTGTTTTTTGA | 23607 |
rs202062708 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47570548 | TTATCCTCTTTTCTT[C/T]TTTCCAGTGGCTGTT | 23607 |
rs202063160 | in-del | -/G/TG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47610986 | TTTTTTTTTTTTTTT[-/G/TG]GAATATAAAACATTT | 23607 |
rs202082790 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47514274 | ATAGTCTACTTCATT[A/G]ATCTTTTTTAAGTCA | 23607 |
rs202146749 | snp | A/C/G | 5.64078e-05 | 0.00531048 | intron-variant | CD2AP | GRCh38.p7 | 6:47624148 | ACTACTAAACTAAGG[A/C/G]TATTTTATGTTTGCT | 23607 |
rs202157393 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47607126 | CATCCATGTTGCAAA[C/T]GACAGGATCTCATTC | 23607 |
rs202167003 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47549076 | ATAAAAGCCGTCTAT[A/G]CAAAACCACAGCCAA | 23607 |
rs202167087 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47607136 | GCAAATGACAGGATC[G/T]CATTCTTTTTTGTGA | 23607 |
rs202187543 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497148 | TCGTGTTTTTTTTTT[-/T]ACTGTGAAGCCAAGT | 23607 |
rs202232574 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47512473 | CTATACTGAAGAACA[A/G]TGATAGTCAAATTGG | 23607 |
rs202236302 | snp | C/T | 0.000363108 | 0.0134693 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47579459 | AGACAATTTTGCTGT[C/T]CAGATAAATGAACTT | 23607 |
rs207466929 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47542768 | AATAAGCCTGGCCCT[A/G]TGCTAGGTGCTGGGT | 23607 |
rs267606710 | snp | A/C/T | 5.22929e-05 | 0.00511314 | CD2AP | 6 | allele_origin=T(germline)/C(germline) | 6:47612492 | GAACTGGAAAAACTG[A/C/T]GAAAAGATTTGGAAG | 23607 |
rs367547554 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47482182 | AAAACAATATTAGGA[A/C]ATTTTTGTTTCAAAG | 23607 |
rs367549725 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47501299 | TGTATGTTTAATTGT[A/G]TGTGATTAAGGTTGC | 23607 |
rs367575812 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47537023 | AGTAGTGGAAACTCA[C/T]GCTACAGCAGAAGTG | 23607 |
rs367579547 | in-del | -/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476878 | CTGCCTGGATCCAAA[-/G]GGCAAGTCAGTTTCA | 23607 |
rs367584453 | snp | A/C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47515517 | AATGTGTCATTCTTA[A/C/G]CCAAAGTCTTGCTGG | 23607 |
rs367618571 | in-del | -/CAT | 0.00557542 | 0.0525036 | intron-variant | CD2AP | GRCh38.p7 | 6:47479872 | CTGATTAGTGTCCCC[-/CAT]CATCTTTCCTTTTCT | 23607 |
rs367676816 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47508048 | AGTTTTAGCATAATT[C/G]TTAAGGACCCTAGGA | 23607 |
rs367677085 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47551542 | AAAACCTAAGAAGAT[A/G]GGTATTTTTATCCCC | 23607 |
rs367678436 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47583083 | CCTCCGTGCCTGGGC[C/T]AGTATCATTTTTTTA | 23607 |
rs367696400 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47572886 | GAATAAATGGTAACT[A/G]CTATTTTTATTGTCC | 23607 |
rs367696736 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47616243 | ACTGTAGGCACGTGC[C/T]ACCATACCCAGCTAA | 23607 |
rs367701263 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CD2AP | GRCh38.p7 | 6:47593271 | AAAATTAAAAACTTA[C/T]ATGCATTAAAGGACA | 23607 |
rs367704926 | snp | C/T | | | intron-variant, downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47603973 | TTGGTTTTCCATTTT[C/T]AGATACAATGAAATT | 23607 |
rs367721157 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47583427 | TCTACCTATTCATCT[A/G]TCCTTCCCTTCAACC | 23607 |
rs367763749 | snp | C/G | 5.04749e-05 | 0.00502343 | intron-variant | CD2AP | GRCh38.p7 | 6:47608050 | TGCATTGTGGTCTAA[C/G]GTTTGTTGACTTTCT | 23607 |
rs367767906 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47513601 | CAGTATTATAGGAGA[A/G]ACACCTTTACTACTA | 23607 |
rs367796574 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CD2AP | GRCh38.p7 | 6:47532813 | GAATTGCATTGATAT[A/G]TTACATCAATTTTAA | 23607 |
rs367809257 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47568070 | GCACAAAGAACAGGA[A/C]CTAGTGATAATGTTA | 23607 |
rs367815070 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47599179 | TGCGTTTATGGAAAT[A/G]GTTTTACAGAACAGA | 23607 |
rs367838615 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47492746 | CTTCTGTTTTTCCCC[C/T]TGGTCATTCTTTCTA | 23607 |
rs367887653 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47573911 | AAATTGCATAAATTG[C/T]ATCTTGCTCTTCTGG | 23607 |
rs367905469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47592449 | TAGGTTTTTAGATAC[A/G]TGTGATATTGTGATC | 23607 |
rs367908314 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626230 | AGTTTTTGCTTGTGT[C/T]CTCCTCAGTCAGAAT | 23607 |
rs367923558 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47548088 | AAAAGTTAAAAGTTG[A/G]TGCCTACATCAAAGA | 23607 |
rs367930720 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47561040 | ATTCATCAGGTATCA[C/G]TCTATTACCAGTATT | 23607 |
rs367934990 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47616972 | CTTTTTTTACTTTTT[A/T]AATTTTGTTTTTAGA | 23607 |
rs367936789 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47539756 | ATGCAGTATGTCCCC[A/G]CCTTTGCTGTACCTC | 23607 |
rs367938191 | in-del | -/TCT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47607129 | CATGTTGCAAATGAC[-/TCT]AGGATCTCATTCTTT | 23607 |
rs367946683 | snp | A/G | | | utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47477947 | ACTGCGGGAGCGGCC[A/G]GGGTGGGAAAACCGC | 23607 |
rs367952819 | snp | A/G | 0.000214612 | 0.0103566 | missense | CD2AP | GRCh38.p7 | 6:47503301 | ATATTGTGGAGTATG[A/G]CTATGATGCTGTACA | 23607 |
rs367962349 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47506295 | GGATGGCGGCCGGGC[A/G]GAGACGCTCCTCACT | 23607 |
rs367966881 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47531477 | TGAGGGGAAACAGGA[A/G]GATTGTTTATTTAAG | 23607 |
rs367970177 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47572332 | CTTGTTGTATTTACA[C/T]GGTGCGACATTTGTC | 23607 |
rs368011774 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47484617 | TAGAACCTGTCCTTT[C/T]CAGTGGCTCCAGTAG | 23607 |
rs368049828 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47501934 | AAACTTAGTAGTTTA[G/T]AACTATATATATTTA | 23607 |
rs368107857 | snp | C/T | 3.31115e-05 | 0.00406874 | intron-variant | CD2AP | GRCh38.p7 | 6:47574262 | AAAAGGTGGTAATGA[C/T]GGACTTGTTAGATTA | 23607 |
rs368112272 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47598357 | AGATTCCTTAAAGAA[C/G]TAAAAGCAGATCTAC | 23607 |
rs368119147 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47566937 | TGTAAACATATGCAT[A/G]CATGTGTCTTTATAG | 23607 |
rs368124284 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47552692 | CCAGTTGGGGTTCCA[A/G]GTATAGGTAATAGAC | 23607 |
rs368127036 | in-del | -/TG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47564323 | TAAAGCATATGAGTG[-/TG]AAATGATCTTTGTGA | 23607 |
rs368150114 | snp | C/T | 3.29777e-05 | 0.00406051 | missense | CD2AP | GRCh38.p7 | 6:47609246 | AATTCCCTGGATGAA[C/T]TTAGAGCCCAGATTA | 23607 |
rs368223879 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47609514 | AAACCCCATCTTTGC[-/A]AAAAAAAAAAAAAAA | 23607 |
rs368235654 | in-del | -/CGT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47597791 | GGCAGGTACTGGTGT[-/CGT]GGAGTTTGGGACTGT | 23607 |
rs368254241 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47570618 | CTCTCTGTCACTTAA[G/T]GGTTCTCAGTGATAC | 23607 |
rs368257499 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47480681 | CACTGCCAGTGCTGG[C/T]GGTGGTGATTTTCAT | 23607 |
rs368258689 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47533221 | GTGTTGATGGTTGCA[A/G]CAGAAAGTGTATGGT | 23607 |
rs368290747 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47607563 | GTTGTGAAATATTCA[-/T]TTGTTTTTGTAGTAC | 23607 |
rs368301949 | in-del | -/CTTTT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47508534 | AAACTTTCTTTCTTT[-/CTTTT]TTTTTTTGTTTTTTT | 23607 |
rs368341085 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47588466 | ATTCCAGATTATGAC[A/G]TGTTTACATTTGTTT | 23607 |
rs368356005 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47561439 | TGAACCTTCCCTACC[C/G]TAGTCTTGGAATCAG | 23607 |
rs368366749 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47554853 | TTTTTGAAACTCTGT[C/T]CTTTCTTTTGAACTT | 23607 |
rs368370766 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47583941 | ATTTTAAGTGTTTTG[C/G]ATTTTGGCCTTTCTA | 23607 |
rs368396583 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47524706 | AGTGAATTTATATAA[C/G]TTCCCCCACCCCATT | 23607 |
rs368408367 | snp | A/G | 0.000415093 | 0.0144005 | intron-variant | CD2AP | GRCh38.p7 | 6:47503453 | AAGGTAAGTATTTTC[A/G]GTTAAATTTCTAGCT | 23607 |
rs368440056 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47534951 | AGGTGTGTGCCACCA[C/T]GTCTGCTAATTTTTG | 23607 |
rs368446702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47622026 | TCTTGCTGTGGCTGC[C/T]GTTGGGGATGAAGGT | 23607 |
rs368451359 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47579007 | TTTAACGTTATAAAT[A/G]GAATTTTAAAATTGA | 23607 |
rs368514132 | snp | A/G | 0.000182386 | 0.00954777 | intron-variant | CD2AP | GRCh38.p7 | 6:47576517 | ATGCCATTTTTTTCT[A/G]TTCTAGCCCTTAATC | 23607 |
rs368614459 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47490731 | ACATTAGGAAGAATA[G/T]AATACTGTGTAAAAA | 23607 |
rs368625599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47482268 | TTTTTTGAGGTTTCA[A/G]AATTTGAGTAGTTTA | 23607 |
rs368666602 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47540280 | CCTCTCTTCTTTTTT[-/T]GTGCTTAGCATGGGT | 23607 |
rs368708157 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47612449 | AATCGAAAGACTTAA[C/G]AGTAATAAGTACTTT | 23607 |
rs368725872 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47499030 | TCAAAATGTCCTGAT[G/T]TGGCCAGTAAGAACC | 23607 |
rs368735239 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47572974 | CATATTTTTCCTTAC[C/G]CCGTACCCCCGGTCT | 23607 |
rs368742780 | snp | A/G | 1.65356e-05 | 0.00287533 | intron-variant | CD2AP | GRCh38.p7 | 6:47581999 | TTAATGTTTTTTCCC[A/G]TAGCTCCAAAGCCTG | 23607 |
rs368757596 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47596957 | AAAGTTAAAGTTTAT[A/T]TTAATGTTGTAAATA | 23607 |
rs368773078 | in-del | -/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47553538 | TTTTTTTTTTTTTTT[-/G]TATTTTTAGTAGAGG | 23607 |
rs368795308 | snp | C/T | 4.96619e-05 | 0.00498282 | stop-gained | CD2AP | GRCh38.p7 | 6:47533686 | GCAAGTCTTGTACAA[C/T]GAATAAGCACCTATG | 23607 |
rs368857658 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47549481 | AAAAAAAAAAAAAAA[-/T]AAGATGCTTAGGAAT | 23607 |
rs368861804 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47582804 | TGTTTTGTTTTTTTT[G/T]TTTTGTCTCGCTCTC | 23607 |
rs368907487 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47618051 | TGGCCGGGCACGGTG[C/G]CTCACACCTGTAATC | 23607 |
rs368915793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47575093 | TATTTTCTTATGTAG[C/T]AGTGAAGAGTTGGGT | 23607 |
rs368923662 | snp | C/G | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47477686 | GCAGCCGTGGGGACC[C/G]GGAGAGAGCCCGAAC | 23607 |
rs368925295 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47550455 | GAAGACATGTTCAAC[A/G]TCACCAATTATCAGG | 23607 |
rs368926176 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47606958 | TCCCCCCATCCCTAC[C/T]GCCACCACACTAACA | 23607 |
rs368928855 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47605123 | TGACAGAAAGTATTA[C/T]AAACATCTAGGCAGA | 23607 |
rs368945780 | in-del | -/TGTGTA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47491266 | TTCCTGATATGTGTG[-/TGTGTA]TGTGTGTGTGTGTGT | 23607 |
rs368985162 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47589569 | ACACACACACACATA[C/T]ATATATATATATTTG | 23607 |
rs368991423 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47562826 | TGGTGGAGGCCCTTG[G/T]TGCTGAACACCAAAT | 23607 |
rs368992030 | in-del | -/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47484366 | CTTTTTTTTTTTTTT[-/G]TTATGTTTTGGTTTT | 23607 |
rs368993148 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47561794 | TATTTATTTATGTAT[G/T]TATTGAGACGGAGTC | 23607 |
rs368995533 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47489633 | GCTAGGCTGAATGTA[C/G/T]GGAGCATTCGGTTCC | 23607 |
rs369041011 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47528017 | TGTTTTATATATGTG[A/G]TGTTGTAAAATTGGT | 23607 |
rs369074436 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47584804 | GATCAGTTTTTAGTA[C/T]TTGTTTATAATATCT | 23607 |
rs369087971 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47532142 | TTTATAATCATAAGA[A/C]TTTATAAACTTGAAA | 23607 |
rs369098592 | snp | A/C | 1.66485e-05 | 0.00288513 | intron-variant | CD2AP | GRCh38.p7 | 6:47609343 | GTGAGTACTACTTAA[A/C]CCATGCATAAAGAAT | 23607 |
rs369135803 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47538543 | AAGCCACTGCGCCTG[A/G]TGGAGAAAGAACTTT | 23607 |
rs369187411 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47547413 | AAACTTTAAATCAAC[A/C]GCAGTTTAAAAAGAC | 23607 |
rs369220847 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47486170 | ATTAATGTCATGTTA[A/G]ATGCTTGGGGGTTTA | 23607 |
rs369236630 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47514962 | GAGGCTGAGGCAGGA[G/T]AATTGCTTGAACCCA | 23607 |
rs369305476 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47622140 | GGAAAGCTGGCAGTC[A/C]CAGGCCTCACCCAGC | 23607 |
rs369315509 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | CD2AP | GRCh38.p7 | 6:47624119 | TCACATCTTAATGAC[A/G]TAGAGTAAAATAAAC | 23607 |
rs369316183 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47601256 | CTATATAGTAAACAG[A/C]GACTTTGTGGAACAG | 23607 |
rs369349511 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47549718 | AAAACAATTCTAAAA[C/T]TCATATGGAACCAAA | 23607 |
rs369459203 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47514922 | CCAGGAGTGGTGGCA[C/T]GCACCTGCAATCCCA | 23607 |
rs369461060 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47478492 | GCCTCTTTTCCTGTT[C/G]ACCAGAAAGGTGCGG | 23607 |
rs369465719 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47507869 | TACATTTCCAACAGA[C/G]CTCTTGGGTGATCAG | 23607 |
rs369507527 | in-del | -/AGTACTG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47486568 | AGTGATGATATACTG[-/AGTACTG]GCAGTAGTTAAGGTA | 23607 |
rs369536196 | snp | A/G | 0.000280924 | 0.0118483 | intron-variant | CD2AP | GRCh38.p7 | 6:47596029 | CTCCTATAGCCAAGT[A/G]AGTTTTACCTAATTT | 23607 |
rs369561625 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47567956 | TGAGCTGCTGACGCC[A/G]GTTGAGAATGTTTTG | 23607 |
rs369594344 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47523296 | TTAAATGGAAGACAA[A/G]TTTACTGGCTAATTG | 23607 |
rs369595595 | snp | A/T | 0.000153988 | 0.00877327 | intron-variant | CD2AP | GRCh38.p7 | 6:47576993 | TGAGCCACATTATTT[A/T]CATTCTTTATTTCAG | 23607 |
rs369674049 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47589379 | AGGAACTCTTGAATA[C/T]ACACACACACACACA | 23607 |
rs369749307 | in-del | -/A/AA/AAA | 0.375399 | 0.216275 | intron-variant | CD2AP | GRCh38.p7 | 6:47488723 | AGACTCCATCTCTCC[-/A/AA/AAA]AAAAAAAAAAAAAAA | 23607 |
rs369753088 | snp | C/G | 0.000153988 | 0.00877328 | missense | CD2AP | GRCh38.p7 | 6:47577082 | TTTTAAAGAGGGGGA[C/G]ATAATCCATTTGATA | 23607 |
rs369804660 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47484402 | CTGAAGGTCTCAGCT[C/T]CCTAGATGTTCTACA | 23607 |
rs369808601 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47524777 | ATAGGAAGTTCCTTT[G/T]TCCAAAATGTGGAGA | 23607 |
rs369808705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47546360 | TGGGATTATGTTAAA[C/T]GACCAAACGTAAGAA | 23607 |
rs369813356 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47503801 | TACTTGTGAAATAGT[A/T]ATGACAGATAGTAGC | 23607 |
rs369818712 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47502468 | GGGTTTTGTTGTGTT[G/T]CCCTGGCTGGCCTCG | 23607 |
rs369859641 | snp | A/T | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624594 | TTACAAGTAATCTGT[A/T]AAGATATACTATTTG | 23607 |
rs369878862 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CD2AP | GRCh38.p7 | 6:47483409 | AGAGATTCAGACTGG[C/T]ATCTTGGGGGAAAAG | 23607 |
rs369889247 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47519006 | TATCTATTTGCCACT[C/G]ATTTATTTATTCAGA | 23607 |
rs369896972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47528381 | GGTTTTGTCATGTTC[A/G]CCAGGCTTGTCTTGA | 23607 |
rs369900668 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47527713 | AAGCTGCTTGGAGTA[C/T]GTTGAGTGATACCTG | 23607 |
rs369931382 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47528647 | GAAATACAATAAAAC[A/G]TAATCCCTTCTGTCC | 23607 |
rs369932026 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47539226 | TTGATAAATGTTTAC[A/G]GTTATTCTGGTGTTT | 23607 |
rs369974592 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47585928 | TTGGAAATACGGCCA[A/G]CAAATTCCAGAATAA | 23607 |
rs370000370 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47549360 | TTCAGCAAAGTTTCC[A/G]GGTACACAATTAATG | 23607 |
rs370009745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47509378 | AAGGGAGCCCATGCC[A/G]TTGGAAAAATGGCAT | 23607 |
rs370020205 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47617180 | ATGTTGCCCAGGTTG[A/C]TCTTGAACTCCTGGC | 23607 |
rs370038316 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47573036 | TGTTTCTTACTTAGA[G/T]TATAAGGCTCTTTGA | 23607 |
rs370045595 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47494311 | TTTCTTTGGGTTTCC[C/T]TAAGAACTCTTTCTC | 23607 |
rs370120847 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47596094 | TAATGGCTCTATTGC[A/C]TTTCTAAATCTCCAG | 23607 |
rs370143870 | snp | A/G | 0.00335688 | 0.040831 | intron-variant | CD2AP | GRCh38.p7 | 6:47478264 | GTAAGAGACTCGGGC[A/G]CTTCCCGCCGCCCGT | 23607 |
rs370145728 | snp | A/G | 1.75259e-05 | 0.00296017 | intron-variant | CD2AP | GRCh38.p7 | 6:47579531 | AATACTTGAAAGAAC[A/G]TTTTGCCACTATTCT | 23607 |
rs370147689 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47565688 | CTTCTTTTTAACCTC[A/G]CACCCTACCATGATT | 23607 |
rs370153974 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47607490 | TCTTTTGGATAAAAA[C/T]CATTTTAATTGGGGT | 23607 |
rs370172226 | in-del | -/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47500122 | ATTGCTCTGAGAAAC[-/C]AGCATTCATCCATAA | 23607 |
rs370205017 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47564328 | GCATATGAGTGAAAT[G/T]ATCTTTGTGATGCCA | 23607 |
rs370207113 | snp | C/T | 3.43342e-05 | 0.00414318 | intron-variant | CD2AP | GRCh38.p7 | 6:47599295 | CGTGTTTTTTTCTTA[C/T]TTCAGGATTAATGGG | 23607 |
rs370207752 | snp | A/G | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520350 | CTAAAGAGGAAATCT[A/G]TGCTGAAAAAAGTGA | 23607 |
rs370213675 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47619597 | CCAGTAGTGGGATTG[C/T]TGGATCAAATGGTGG | 23607 |
rs370230334 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47500896 | GGGACTACAGGCGCC[C/T]GCCACCACGCCTGGC | 23607 |
rs370307845 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47505557 | GGCACACCTCCCAGA[C/T]GGGGTGGTGGCTGGG | 23607 |
rs370309264 | in-del | -/CAA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47609513 | AAAACCCCATCTTTG[-/CAA]AAAAAAAAAAAAAAA | 23607 |
rs370335632 | snp | C/T | 0.000248639 | 0.0111471 | intron-variant | CD2AP | GRCh38.p7 | 6:47576520 | CCATTTTTTTCTATT[C/T]TAGCCCTTAATCCTA | 23607 |
rs370345124 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47540696 | CATTGACTTGCCTGG[G/T]TTGGGGCTAATGAGT | 23607 |
rs370362627 | in-del | -/TCC | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497246 | CCTTTTCCTTTTCTT[-/TCC]TTTTCCTTTCCTTCC | 23607 |
rs370367704 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47543041 | CTGTAATCCCAGCTA[C/T]TCAGGAGGCTGAGGC | 23607 |
rs370386157 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47506809 | GGAGGGAGAGGGAGA[C/G]GGAGAGGGAGAGGGA | 23607 |
rs370400344 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47510998 | GAATTGCTTGAACCC[C/G]GGAGGTAGAGGTTGC | 23607 |
rs370436090 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | CD2AP | GRCh38.p7 | 6:47500430 | CAGCTGTGCATCCCC[G/T]TTCAGACATTTGTTA | 23607 |
rs370447109 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47534079 | TGAAATATCTGCTGA[G/T]TCTTAGCATAGATAC | 23607 |
rs370478848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47541146 | TTTTATTTTTTGAGA[C/T]GGAGTCTTGCTCTGT | 23607 |
rs370479237 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47620574 | GAATTGTTTTTTCCA[-/A]TTCTGTGAAGAATGA | 23607 |
rs370486072 | in-del | -/CAC | | | intron-variant | CD2AP | GRCh38.p7 | 6:47551127 | AATCTCACAAATCAC[-/CAC]TAAAGAACTTACTTA | 23607 |
rs370492851 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47586476 | AGAATGGGGACATGA[A/G]AAAACTTAAAGAAAT | 23607 |
rs370508716 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47542123 | CAGTTCAAACCTGTC[C/G]TTTCTAATTTTTGAA | 23607 |
rs370531782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47523435 | ATTTAGAGAAAAGAA[C/T]AGATCTCCATTTCCA | 23607 |
rs370551902 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520632 | GGGCGAAAGTGGGGT[A/C]TATGGTGGTGATTGG | 23607 |
rs370585821 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47623850 | TTTAATTATAGATAC[A/C]TGTACATTTCTTAAT | 23607 |
rs370673360 | snp | C/T | 3.29919e-05 | 0.00406138 | missense | CD2AP | GRCh38.p7 | 6:47503418 | ATGGGAGAAGAGGAA[C/T]GTTCCCTGACAATTT | 23607 |
rs370679749 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47524813 | TGTGTAACAAAAAGC[A/G]TAGTAGAGGAGAGAA | 23607 |
rs370681671 | snp | C/T | 1.66738e-05 | 0.00288732 | intron-variant | CD2AP | GRCh38.p7 | 6:47607892 | TTTCTTTTCTTTGGT[C/T]TATTATGTCTCTTGA | 23607 |
rs370684065 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47492371 | TTTTTTTTTTTTTTT[G/T]AGACAGGGTCTTGCT | 23607 |
rs370689673 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47535770 | AGCTGAACCTCTATA[C/T]AGAATGTCTGTGCTG | 23607 |
rs370701011 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47623384 | GATGATCAAAATGTT[A/G]TAGAATTGAGAAGAG | 23607 |
rs370740553 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47485622 | TGGTGTTTATAAAAT[A/C]TATAGTAGTGTATAC | 23607 |
rs370763335 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47509375 | ATAAAGGGAGCCCAT[A/G]CCGTTGGAAAAATGG | 23607 |
rs370780715 | snp | A/T | 1.65239e-05 | 0.00287431 | intron-variant | CD2AP | GRCh38.p7 | 6:47580921 | TAAGAAGCATATTAT[A/T]CAGTTTGCTATTTTC | 23607 |
rs370791689 | snp | C/T | 4.98326e-05 | 0.00499138 | intron-variant | CD2AP | GRCh38.p7 | 6:47576501 | TATCTTAAAATAGTT[C/T]ATGCCATTTTTTTCT | 23607 |
rs370801294 | in-del | -/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47609513 | AAAACCCCATCTTTG[-/C]AAAAAAAAAAAAAAA | 23607 |
rs370806287 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47614753 | TGAAGCACAGCAAAA[C/T]GAAGTACAATAAAAA | 23607 |
rs370844314 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47494993 | AATGAGACCATGTCT[C/T]TACAAAAAAATTTCA | 23607 |
rs370852801 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47615380 | GAGACTGGATAATTT[A/G]TAAAGAAAAATTTAA | 23607 |
rs370855299 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47529717 | TCTTGTTTATGTCAA[C/G]TAGCCTATGCTAAAA | 23607 |
rs370876825 | snp | A/C/G/T | 6.82175e-05 | 0.00583997 | intron-variant | CD2AP | GRCh38.p7 | 6:47606123 | TTTACCTTTAAAAAG[A/C/G/T]TACAGTTCTCTTAGT | 23607 |
rs370884074 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47597790 | AGGCAGGTACTGGTG[G/T]CGTGGAGTTTGGGAC | 23607 |
rs370888217 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47615162 | GGGGACTTGCAGTTG[A/G]AAAACCTTGGCTCTT | 23607 |
rs370888468 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47580467 | CAAAACAAAACAAAC[A/C]AAAAAAAAAACGGTC | 23607 |
rs370890108 | snp | A/G/T | 1.672e-05 | 0.00289132 | intron-variant | CD2AP | GRCh38.p7 | 6:47582096 | AACTTTCAAAAAAGC[A/G/T]ATTATTTCTTTTATT | 23607 |
rs370905500 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47623486 | GTGGAACATTGGCAT[A/C]CTGTTTAATGTCTTT | 23607 |
rs370906372 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47502493 | CCTCGAACTCCTGAG[-/T]TTTTTTTTTTTTTTT | 23607 |
rs370926805 | snp | A/G | 4.96446e-05 | 0.00498195 | intron-variant | CD2AP | GRCh38.p7 | 6:47581989 | TAAAAAAGTATTAAT[A/G]TTTTTTCCCATAGCT | 23607 |
rs370948714 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47619022 | GTTCACTAAAAATGA[A/T]CAATGAACATACAAG | 23607 |
rs370960779 | snp | A/G | 1.65452e-05 | 0.00287616 | intron-variant | CD2AP | GRCh38.p7 | 6:47580839 | TGAAACTGGTCAGCC[A/G]TTTCCACCATTATTA | 23607 |
rs370963225 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47538386 | AGCTGGGATTACAGG[C/T]GTGCACCACCATGCC | 23607 |
rs370972520 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47592951 | TCATGGGAATCCCCA[A/G]TTTATAGCCAATTGA | 23607 |
rs370986681 | in-del | -/T | 0.00993419 | 0.0697739 | intron-variant | CD2AP | GRCh38.p7 | 6:47605837 | GGAACTTAAGATGAG[-/T]TTTTTTATGCTACTA | 23607 |
rs371036684 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47499620 | TCTCCTGGTAGTTTT[A/C]CAGTTTATGATGGGT | 23607 |
rs371058774 | in-del | -/T/TT/TTT | 0.615951 | 0.13763 | intron-variant | CD2AP | GRCh38.p7 | 6:47557169 | CACCTTTTGATGGAG[-/T/TT/TTT]TTTTTTTTTTTTTTC | 23607 |
rs371130008 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47530611 | GAGTTTTTGGATATT[C/T]ATTACACTGAATTTT | 23607 |
rs371138620 | snp | A/G | 1.78726e-05 | 0.00298931 | intron-variant | CD2AP | GRCh38.p7 | 6:47599266 | AAAGTCGTGTTTCAT[A/G]CTAGTGATTTTTGCG | 23607 |
rs371139492 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47512144 | GCCTGGGCAACAGAG[C/G]GAGACTCCGTCTGAA | 23607 |
rs371140357 | snp | C/T | 0.000115755 | 0.00760685 | intron-variant | CD2AP | GRCh38.p7 | 6:47581998 | ATTAATGTTTTTTCC[C/T]ATAGCTCCAAAGCCT | 23607 |
rs371263144 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47505346 | GCACAGGGTTGGGGG[C/T]AAGGTCACAGATCAA | 23607 |
rs371293071 | snp | A/C/G | 0.000248266 | 0.0111389 | missense | CD2AP | GRCh38.p7 | 6:47533687 | CAAGTCTTGTACAAC[A/C/G]AATAAGCACCTATGG | 23607 |
rs371323070 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47611641 | GCTGTTATTTCTACA[A/G]TATTCTCAAGAATTT | 23607 |
rs371337305 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47567117 | TTACTATGCTGTTTA[A/G]CATATGGGGTATGGA | 23607 |
rs371356544 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47597665 | CCCAAAACTAAAACT[A/G]AAATGGAAGTACAAG | 23607 |
rs371362953 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CD2AP | GRCh38.p7 | 6:47560211 | TATCATTCACCTTCT[A/G]TCTAGATATCTGTAT | 23607 |
rs371385059 | snp | C/G | 3.336e-05 | 0.00408398 | intron-variant | CD2AP | GRCh38.p7 | 6:47582087 | CTAATTTTCAACTTT[C/G]AAAAAAGCAATTATT | 23607 |
rs371396990 | snp | A/T | 1.64963e-05 | 0.00287192 | intron-variant | CD2AP | GRCh38.p7 | 6:47574029 | GCGTTTTGTGATTCT[A/T]GGTGTCATTCTTCAA | 23607 |
rs371421875 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497218 | TTTTTGCTTTCCCCT[C/T]TTTCCTTTCCTTTCC | 23607 |
rs371425328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47536536 | AGTATCCAAAAACTG[A/G]ATTGGACTAGTGAGC | 23607 |
rs371434430 | in-del | -/G | 0.00676609 | 0.0577691 | intron-variant | CD2AP | GRCh38.p7 | 6:47554939 | TGAATTAAATATCTA[-/G]TCCAATAATTTAATA | 23607 |
rs371476304 | in-del | -/CA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47600986 | AAAATCTGGAATCCA[-/CA]TCTTGCTTTGTATTC | 23607 |
rs371492573 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47522318 | AAAGAGTGTTAGCAG[G/T]ACAGTATTTGTTGAT | 23607 |
rs371503675 | in-del | -/AATG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47589395 | ACACACACACACACA[-/AATG]TATATACACACACAT | 23607 |
rs371504280 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47543632 | GTATTGGAGGGTTGG[A/G]GAGGGCAATGGTGGG | 23607 |
rs371513357 | snp | A/C | | | downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47627330 | TGAAACTGAGACAGT[A/C]ATTTCTACTTTACAG | 23607 |
rs371517849 | snp | A/G/T | 0.00035944 | 0.0134013 | intron-variant | CD2AP | GRCh38.p7 | 6:47609115 | AAATTTTTTTTTTAC[A/G/T]TTTTCAGCCATCTGT | 23607 |
rs371520735 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47518923 | TTTTAGAAAGAGACA[C/T]GGTAGTACTGTGGCA | 23607 |
rs371522449 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | CD2AP | GRCh38.p7 | 6:47607919 | TTGACTTCTAAAAAA[C/T]CATTTAGCCAACTCA | 23607 |
rs371524963 | in-del | -/GTTT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47578045 | ATAGTTACCTTTTTT[-/GTTT]TAGTGGCAATAGCAG | 23607 |
rs371541074 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47509987 | GAATGATTTATCATG[A/G]AACTCCATTTTGAAA | 23607 |
rs371542865 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497321 | TTTTCCTTTCCTTTC[A/C]TTTCCTTTCCTTTCC | 23607 |
rs371570657 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47575891 | CTGGGTTAAAATCTG[C/G]GCTTTGCTGCTAAAT | 23607 |
rs371574777 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47513776 | AGCTGAAGATTTGCT[A/G]ACTCCTAGGGTGTGC | 23607 |
rs371575952 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47553086 | TTGTATTGTAGCCAT[C/G]TGCTTATTGATTTTT | 23607 |
rs371586026 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47599782 | TTAAAAGTTTAAAAA[G/T]GAGATGACATAGACT | 23607 |
rs371605110 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47613265 | GAATTTTTTCCAAAT[A/G]GTTTTCAGTTTATTT | 23607 |
rs371719248 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47616407 | CCTTAAAGATGTTTT[C/T]AACAGAAGCAACCAA | 23607 |
rs371719452 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47593548 | AGTAAGCACTTGACA[A/G]GATGTTTAATATCAT | 23607 |
rs371723532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47588955 | GTCTCAGTGTAATCA[C/T]ATGAAAGTAGGATTG | 23607 |
rs371754388 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47548402 | CAGAAATACAAAAGG[A/T]CATTCAAGGCTACTG | 23607 |
rs371763351 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47580124 | ACTCTATGGAAGCTT[-/T]AGGCTGTCTGAGGCC | 23607 |
rs371806727 | snp | A/G | 0.000588639 | 0.0171456 | intron-variant | CD2AP | GRCh38.p7 | 6:47554812 | TTAAATAAACTTTAT[A/G]TAGCATCTAGTGTTT | 23607 |
rs371889867 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47583459 | TTGTCAACCATTAAT[A/T]TTTTTAATGACTCCA | 23607 |
rs371926505 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47606584 | AGTTATTAAAATTGA[A/G]CAGCAGATACTCACT | 23607 |
rs371933675 | in-del | -/TTC | | | intron-variant | CD2AP | GRCh38.p7 | 6:47607131 | TGTTGCAAATGACAG[-/TTC]GATCTCATTCTTTTT | 23607 |
rs371935130 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47555815 | AATAATTTTTTTTTT[A/T]ACGTGAAAGGGCTGT | 23607 |
rs371968297 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47502856 | GGGATTATAGGAGTG[A/G]GACATTACGCCCTGC | 23607 |
rs372001958 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47589399 | ACACACACACAAATG[C/T]ATATACACACACATA | 23607 |
rs372057213 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47574772 | TTCATTAGCATTTTG[C/T]TGGCATTGTGAAATG | 23607 |
rs372058363 | snp | A/C/G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47620278 | TCATTCTCCTACATG[A/C/G/T]GGCTAGCCAATTATC | 23607 |
rs372069157 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47566536 | ATACATATGCAGAAC[A/C]TGCAGGTTTGTTACA | 23607 |
rs372078669 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47518430 | GTCATTCTAGATTAG[C/T]TTTGCTTTTATAATA | 23607 |
rs372095479 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47516384 | CTGGAAGTGGTCCAT[A/G]TTACTTTTTCATTTC | 23607 |
rs372101571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47534735 | TGTACAAAGAATTAC[A/G]GTGTTATGGGAGCAC | 23607 |
rs372101737 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47491853 | CAACTAGTAAACCCA[C/T]TAAAAGAATACCTCA | 23607 |
rs372109097 | snp | C/T | 1.64882e-05 | 0.00287121 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47595937 | GAAACCTACTCCACC[C/T]ACCAAAGCCAGTAAT | 23607 |
rs372124604 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47580746 | ATTTTATATTTTGTC[A/G]AGGATTGAATGAAGA | 23607 |
rs372131077 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47482424 | TGCTCTGTCGCCCAG[C/G]CTGGAGTGCAGTGGC | 23607 |
rs372151390 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47518497 | CTGCTCTCCTTTGCT[-/A]AGAAGCATTCCATTT | 23607 |
rs372156497 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47516936 | TTTCTGCCAATATGA[A/G]TTAGTTGCTGGTAGT | 23607 |
rs372156786 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47572729 | GGTCCCTGGGAAAGT[C/T]ATTAATATCCCTTTG | 23607 |
rs372234258 | snp | C/T | 0.000792746 | 0.0198933 | missense | CD2AP | GRCh38.p7 | 6:47609186 | ACTGCTTTCCTGACT[C/T]CATTAGAAATCAAAG | 23607 |
rs372238790 | in-del | -/GA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47506811 | AGGGAGAGGGAGAGG[-/GA]GAGGGAGAGGGAGAG | 23607 |
rs372247205 | in-del | -/AAAAAG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47543181 | AAAAAAAGAAAAAGA[-/AAAAAG]AAAAAAAAGAAAAAG | 23607 |
rs372263135 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47506570 | CTCGGGAGGCCGAGG[C/T]TGGCGGATCACTCGC | 23607 |
rs372340501 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47516353 | AAAATCACGTTCCAG[A/T]TTTAAATGCTTCCCT | 23607 |
rs372350244 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497667 | GATCCACCCACCTCA[A/G]CCTCCCAAAGTGTTG | 23607 |
rs372353832 | snp | A/T | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625172 | TTAGTTCTTCATGTT[A/T]CTCCTTCTGACTTTT | 23607 |
rs372355911 | in-del | -/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47477679 | CCTGGCAGCAGCCGT[-/G]GGGACCGGGAGAGAG | 23607 |
rs372358979 | snp | C/T | 1.64885e-05 | 0.00287123 | missense | CD2AP | GRCh38.p7 | 6:47609253 | TGGATGAACTTAGAG[C/T]CCAGATTATTGAATT | 23607 |
rs372381403 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47588543 | GGATAGTGGAAGGTG[A/G]TATGGGTAAAAGGAA | 23607 |
rs372388284 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47535323 | TTGAAATTATGGTGT[A/G]TAAATCCCTGTAGTA | 23607 |
rs372401485 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47621741 | TTATTGGCCTGTTCA[A/G]GATCTCTAATTCTTC | 23607 |
rs372419564 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47502195 | TGGCCCTCTCTATAG[A/G]TTGGCTTACAGCATA | 23607 |
rs372446289 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47584066 | GTATATCTTTGGTAA[A/G]GTGTTCTGGTCTTTT | 23607 |
rs372479543 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47498188 | TATTGTTGCATGTGT[A/G]AAAATGTTATATCCT | 23607 |
rs372496098 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47532289 | TGGAGGCTGCAGTGA[G/T]CCATGATCATGCCAC | 23607 |
rs372512401 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47569150 | TGATGACAACATATA[G/T]TCAAGATTTGTTTTG | 23607 |
rs372518924 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47595472 | TGTTTTTAGTTCTCT[A/G]TATTTCAGTTTCAGA | 23607 |
rs372552361 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47496926 | AATAGTGTATTTGTG[G/T]ACTTAGCACTTTGTA | 23607 |
rs372563870 | snp | A/G | 0.00016632 | 0.0091177 | intron-variant | CD2AP | GRCh38.p7 | 6:47503457 | TAAGTATTTTCAGTT[A/G]AATTTCTAGCTCTTG | 23607 |
rs372585387 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47488256 | CATTTAGGCATAAAG[C/G]CTTAATTTTTAGCTT | 23607 |
rs372604844 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | CD2AP | GRCh38.p7 | 6:47624144 | ATAAACTACTAAACT[A/G]AGGATATTTTATGTT | 23607 |
rs372647755 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47494962 | CCAAGGAGTTCGAGA[C/G]AAGTCTGGGCAGTAT | 23607 |
rs372718784 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47532980 | CTTAGATCAGGGGCT[A/G]TCAAACTACCAGCCC | 23607 |
rs372758159 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47584208 | TTCTTCACAGAGCAG[A/T]AGTTTTAAATTTGAT | 23607 |
rs372777222 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47567840 | AGTGTTAATCAAATC[A/T]CAGAGAAGCCATAGA | 23607 |
rs372781772 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47621492 | TCATCAAAGATACTG[G/T]TCTGTAGTTTTCGTT | 23607 |
rs372786314 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47546369 | GTTAAACGACCAAAC[A/G]TAAGAATAGTTGGCC | 23607 |
rs372843024 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47554270 | AATTTCCAAATACTT[C/T]AAATAATATACAAAT | 23607 |
rs372843320 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47612013 | TTTTAATTTGTTTGG[C/T]TTTTGGATTTTAATG | 23607 |
rs372879434 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47596252 | CTGTGATAACCTCAC[A/G]TAGTTAACATTTTTA | 23607 |
rs372885089 | snp | C/T | 1.6853e-05 | 0.0029028 | intron-variant | CD2AP | GRCh38.p7 | 6:47606296 | AGTTCATCTAATTGT[C/T]GTAAACTACAGTATA | 23607 |
rs372917311 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47512362 | AAACAAACATAAAAA[C/G]GTGCATGTTATTTTG | 23607 |
rs372921020 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47528446 | TCCCAAAGTGCTGGG[A/G]TTATAGGCATGAACC | 23607 |
rs372951644 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47514128 | GCTTATGTATTCCTC[A/G]TAAATGCTTTTTGTG | 23607 |
rs372960999 | in-del | -/T | 0.42803 | 0.175514 | intron-variant | CD2AP | GRCh38.p7 | 6:47582780 | ATCATGTTTTTTTTG[-/T]TTTTTTTTTGTTTTG | 23607 |
rs372981648 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47591423 | TGAGATAAATACGAA[A/T]AAATATATTTTGTCC | 23607 |
rs372992128 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47547389 | AGCTATGCTTATATC[A/G]GACAAAACAAACTTT | 23607 |
rs373000859 | snp | A/T | 3.38708e-05 | 0.00411512 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624262 | CATAATGTTCCAGGG[A/T]TTCAGAAGCAACGCT | 23607 |
rs373030099 | snp | A/C | 1.64773e-05 | 0.00287026 | missense | CD2AP | GRCh38.p7 | 6:47574084 | GTTTTGGCTGGGCCT[A/C]CTTCACCTATACCTT | 23607 |
rs373037538 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47618391 | ATATAATAACTTCCT[A/G]TATTTTCACTGTTAG | 23607 |
rs373048921 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47508815 | CTCCCAAAGTGCTGG[A/G]ATTACAGGTGTGAGC | 23607 |
rs373069966 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47597231 | TGTTTGTGCTGCTAG[A/G]CATCATGGAGAAAGC | 23607 |
rs373087810 | in-del | -/GT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47556798 | TATGTGTGTGTGTGT[-/GT]CTTTATAGTAGAATT | 23607 |
rs373101562 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47605170 | TAATACAGATCTGGA[C/T]GATTAGACCAAAGGA | 23607 |
rs373162727 | in-del | -/TTTTTTTT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47489165 | ACTGCACTCAACTAG[-/TTTTTTTT]TTTTTTTTTTTTTTT | 23607 |
rs373164575 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47576292 | TTAATATACTATGGA[C/T]GTCAGAGAATATTAT | 23607 |
rs373177642 | snp | C/T | 0.000153988 | 0.00877328 | missense | CD2AP | GRCh38.p7 | 6:47580880 | AACCAAAGAAACCAC[C/T]ACCTCCTGCTAAGGC | 23607 |
rs373182055 | in-del | -/TT | 0.00122276 | 0.0246958 | intron-variant | CD2AP | GRCh38.p7 | 6:47554596 | CCCATAGGGTGACGA[-/TT]TTCACTTAACAGAAG | 23607 |
rs373185402 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47576696 | TTGTTACACTGTCTT[A/T]TTAGAATAGCAAATT | 23607 |
rs373233653 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47600651 | AAATTTATTCGGTAT[C/G]TTTTATATGGTGAAA | 23607 |
rs373258145 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47571372 | CACAGGACTGGTATT[C/T]CTGAGAAAAGGGGAA | 23607 |
rs373259264 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47546742 | ATCAGGTTATCTAAA[G/T]TTAAGATGAAGGAAA | 23607 |
rs373275693 | in-del | -/TCTTTTTTCCTTT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497243 | CTTTCCTTTTCCTTT[-/TCTTTTTTCCTTT]CCTTCCCTTCCTTTT | 23607 |
rs373308184 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47479942 | TGTGATTCTGCATAG[A/G]GGAAAAATCAGTAGG | 23607 |
rs373347653 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47524895 | TGCCGATTTTGATCT[A/G]TTGACACTTAGACGA | 23607 |
rs373444130 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47530069 | TTCTTTCTGTCTCAG[C/T]AGAGATGTCACTTTC | 23607 |
rs373461966 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47490183 | CATAGGGTCTTGCCA[-/T]TATTGCCCAGGCTGG | 23607 |
rs373503672 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47544275 | CTAGCCTAGAGGACT[C/T]GTCTATGATGAATTT | 23607 |
rs373531547 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47613942 | TGTCATGGAGATGGC[G/T]TCTTAAACCACATGA | 23607 |
rs373531644 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CD2AP | GRCh38.p7 | 6:47597221 | GAGATGGACCTGTTT[A/G]TGCTGCTAGGCATCA | 23607 |
rs373532878 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47621950 | ACTAGGGTGGGTAGG[A/G]AAGGGCCATCAGGTT | 23607 |
rs373589026 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47619812 | GATTTACATTTCCCC[A/G]ATCATTAGTGATGTT | 23607 |
rs373623749 | snp | C/T | 0.0196455 | 0.0971431 | intron-variant | CD2AP | GRCh38.p7 | 6:47609096 | TAATATTAAATAAAA[C/T]CAGAAATTTTTTTTT | 23607 |
rs373648714 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47549823 | TATACTATAAGGCCA[C/T]AGTCACCAAAACAGC | 23607 |
rs373663811 | in-del | -/TG | 0.0391387 | 0.134304 | intron-variant | CD2AP | GRCh38.p7 | 6:47556785 | GCTGCATTAAACATA[-/TG]TGTGTGTGTGTGTCT | 23607 |
rs373718197 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47602955 | ATTCGATGGAAGCAT[G/T]CATTGTTGAATAAGG | 23607 |
rs373749831 | in-del | -/CAAAA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47514543 | GTAATTGAGATAAAA[-/CAAAA]TAAACACATTCCAGT | 23607 |
rs373810845 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47616238 | CTAGGACTGTAGGCA[C/T]GTGCCACCATACCCA | 23607 |
rs373844312 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47573511 | TTTTTTTTTTTGAGA[C/T]GGAGTCTTGCCCTGT | 23607 |
rs373884390 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47539326 | TACTGGGGTTGTCAA[G/T]CAGAGTATATTGAAG | 23607 |
rs373888400 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47540175 | GTGAGGCCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 23607 |
rs373926800 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47602811 | AGGCTGAGGTGAGAG[G/T]GTTTCTTAAAGCTGA | 23607 |
rs373962736 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47598301 | TTGTACACTGCTGGT[G/T]GGAATGTAAACTAGT | 23607 |
rs373970967 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47611070 | AAACTGAATGGCAGG[G/T]TTTTTTTTTTTTAAT | 23607 |
rs374067838 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47506011 | CTTCTCAGACGGGGC[A/G]GCTGCCGGGCGGAGG | 23607 |
rs374082001 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47537718 | GAACATCTCAGCAAA[C/G]TAGGCAGTATCTTGA | 23607 |
rs374095933 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47535276 | ATGGGTTAATAGTTA[A/C]TGAATATTTAATCAC | 23607 |
rs374105268 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CD2AP | GRCh38.p7 | 6:47511182 | CTTTACCAAGTGGTC[C/T]AGGTTAATGTCACCA | 23607 |
rs374109627 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47483477 | AGCCACAGGGAAACA[A/G]AATGAGACAGGGTCC | 23607 |
rs374142476 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47566319 | ATATATATATATATA[C/T]ATATACACATACACA | 23607 |
rs374191557 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47532972 | AGCCATGACTTAGAT[C/T]AGGGGCTATCAAACT | 23607 |
rs374239162 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47613671 | AAGGATTTTCAGAAT[A/G]ATAAATAAGTGATGG | 23607 |
rs374273828 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47512972 | ATCTGTTACAAATGG[A/G]TTTTATAACACTAGT | 23607 |
rs374276963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47485295 | TTTTTCACCAGTGGG[A/G]TGAAATATGGAGATG | 23607 |
rs374277420 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47502085 | TGCTTCCAAGCTCAT[A/G]TGTTAGTTTGTATCA | 23607 |
rs374279909 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47529832 | AGATTGCCTACCCAG[A/T]CTCAGAGAGCTTTAT | 23607 |
rs374283826 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47506377 | CGGCCAGGCAGAGAC[A/G]CTCCTCACTTCCCAG | 23607 |
rs374284567 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47508535 | AACTTTCTTTCTTTC[-/T]TTTTTTTTTTGTTTT | 23607 |
rs374436880 | snp | A/C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47610303 | GCCCAGTAGGTAAAA[A/C/T]ATATTTTAAAAAAAG | 23607 |
rs374454366 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47563257 | AATGTGAAGTAAGTA[C/T]GCTAATAGTATAAAA | 23607 |
rs374488678 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47577549 | AACTCTTTTTACTCT[A/G]GAAAATGATGTCACC | 23607 |
rs374493671 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47599175 | GTTTTGCGTTTATGG[A/G]AATGGTTTTACAGAA | 23607 |
rs374501674 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant | CD2AP | GRCh38.p7 | 6:47581991 | AAAAAGTATTAATGT[A/T]TTTTCCCATAGCTCC | 23607 |
rs374511194 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47492729 | ATATAAGTAATCTGG[A/G]CCTTCTGTTTTTCCC | 23607 |
rs374524749 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47615478 | GGCCTCAGGGAGCTT[A/T]TACTCATGGTGAAAG | 23607 |
rs374532164 | snp | A/T | 1.64944e-05 | 0.00287175 | missense | CD2AP | GRCh38.p7 | 6:47579446 | AAGGAGTATTTCCAG[A/T]CAATTTTGCTGTCCA | 23607 |
rs374532922 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47550652 | TTGAGAACTAAAAGT[A/T]GAACTATCACTTGAT | 23607 |
rs374533864 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47570664 | AAAAAAATAATAGAC[A/T]CTGAGCCAGGCACTG | 23607 |
rs374537627 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47487892 | GATTCAGTAATACTT[G/T]AATTTGGAGTAATTG | 23607 |
rs374573835 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47560633 | AGGACTATGGAGTGA[C/T]GATGTCTTATGTAAT | 23607 |
rs374597923 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47490133 | GCATGTGCCATCGCA[C/T]CTGGCTAATTTAAAA | 23607 |
rs374599411 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47509767 | CAAATCACATAATTT[C/T]CCTGTTTTCTCCACT | 23607 |
rs374642083 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47607104 | TTAACATAATGAACT[C/G]TAGTTCCATCCATGT | 23607 |
rs374671796 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47573769 | TGTTGTGGTGGCTCA[C/T]GTCTGTAATCCCAGC | 23607 |
rs374695299 | snp | A/G | 0.000133717 | 0.0081756 | missense | CD2AP | GRCh38.p7 | 6:47533740 | CCACATCCACAAACC[A/G]AAAACATTAAGAAGA | 23607 |
rs374698227 | snp | A/G | | | intron-variant, utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47603893 | AAATAGGTGGTGCAC[A/G]TTGATTTTTCTTTGT | 23607 |
rs374707163 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47583280 | CTTCTTTATCACTCA[A/G]AGTCCATAGTTTCCT | 23607 |
rs374707750 | in-del | -/AGA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47504688 | CAGGGGTACCTTGGA[-/AGA]GATACTGCAGGTTCA | 23607 |
rs374712220 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47565739 | AAATGTTTAGAATCT[A/G/T]TTTTCTTTTTACCAC | 23607 |
rs374751457 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47483332 | TTGGCAAAGTGCAGC[A/G]TGTACATGTATGTGG | 23607 |
rs374756150 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47502653 | CGCCCACCACCATGC[C/T]GGGCTAATTTTTGTA | 23607 |
rs374760994 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47518681 | AGTGGGATTGCTGGG[C/G]TATATAAGAAACTGC | 23607 |
rs374764310 | snp | G/T | 1.70962e-05 | 0.00292366 | intron-variant | CD2AP | GRCh38.p7 | 6:47533759 | ACATTAAGAAGAGTA[G/T]GTAAATAATTCCTTT | 23607 |
rs374768848 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47622284 | AGCTGCGAAAGAAAA[G/T]GGCTTGGTTCTTCCC | 23607 |
rs374818160 | snp | A/G | 4.97335e-05 | 0.00498641 | intron-variant | CD2AP | GRCh38.p7 | 6:47609330 | CTTCTTTTCTCCTGT[A/G]AGTACTACTTAACCC | 23607 |
rs374847632 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47515980 | AATTAGAAAATGAAG[C/T]TTGGCTTGAAATGCA | 23607 |
rs374860589 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47557184 | GTTTTTTTTTTTTTT[C/T]TTGTAAATATGTTTA | 23607 |
rs374914673 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47601226 | TATCTTTTATACATA[A/G]CTGTTATTTACTCCC | 23607 |
rs374922952 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47556107 | GATACATGTACTGAA[C/T]GTGCAGGTTTGTTAC | 23607 |
rs374932764 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47598769 | AAGGGTGGGAGGGGA[A/G]TGAAGGATAAAAGAC | 23607 |
rs374936174 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47490935 | TGTAAGAAATGCTGC[G/T]TATCATTCCATATTT | 23607 |
rs374969272 | in-del | -/GTAA | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47477317 | GCTGCTGATCCGTAA[-/GTAA]CTTCGCAAGGTAAAC | 23607 |
rs374999629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47556504 | AGGCATGTGCCACCA[C/T]GCCCAGCTAATTTTT | 23607 |
rs375006763 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47589150 | TTTCTGGAGGAAACC[A/G]TGTGAATTCAGCTTT | 23607 |
rs375074534 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47615931 | ACTACAGGCGCCCGC[C/T]ACCACACCCGGCTAG | 23607 |
rs375080675 | snp | A/C | 1.65776e-05 | 0.00287898 | intron-variant | CD2AP | GRCh38.p7 | 6:47503447 | TTCGTTAAGGTAAGT[A/C]TTTTCAGTTAAATTT | 23607 |
rs375163856 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47591860 | GGAGACAGGGTCTCA[C/T]TCTGTTGCCCAGGCT | 23607 |
rs375169938 | snp | A/G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47570617 | TCTCTCTGTCACTTA[A/G/T]TGGTTCTCAGTGATA | 23607 |
rs375173164 | snp | A/G | 3.37581e-05 | 0.00410827 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47609131 | TTTTCAGCCATCTGT[A/G]TACCTTTCAACACCT | 23607 |
rs375203011 | snp | C/T | 6.64628e-05 | 0.00576429 | intron-variant | CD2AP | GRCh38.p7 | 6:47576629 | AATAAAGCTTTCATA[C/T]TGGGAATAGTAGAAA | 23607 |
rs375206194 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47606718 | TTTGTATATTTATGG[G/T]TTATGTGAGATATTT | 23607 |
rs375212517 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47584927 | AAAAATCATGTCACC[A/G]GTTAGTCAGCAGTTT | 23607 |
rs375254110 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47545686 | CCACGGATGGTTCAC[A/G]TCACGGGACTCTGTG | 23607 |
rs375261505 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CD2AP | GRCh38.p7 | 6:47552676 | AACTCCTCAGTTGTT[A/G]CCAGTTGGGGTTCCA | 23607 |
rs375268111 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47569742 | AATGGTTGTATACCT[C/T]GTGTGCCAAAGATAG | 23607 |
rs375295422 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47571949 | AGCACTCGTTAAAGT[A/G]GAACTTCTCAACCTT | 23607 |
rs375336671 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47478538 | CGCCTGGCCACCTCT[A/G]CTAACCCCTTGCCCA | 23607 |
rs375338841 | in-del | -/GTT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47499757 | GTTGTTGTTGTTGTT[-/GTT]TTTGAGACAGAGTCT | 23607 |
rs375346046 | in-del | -/GA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47607127 | TCCATGTTGCAAATG[-/GA]ACAGGATCTCATTCT | 23607 |
rs375376540 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47480175 | ACTGAGGGCATTTGT[A/G]GTTAAGTTTTTGTAA | 23607 |
rs375390730 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47530893 | TTGACACTTGTGGAC[A/G]TATATTGCCAGAACT | 23607 |
rs375392156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47617953 | TCTTCTAATGCCCAC[A/G]TTCTACAGATTCTCA | 23607 |
rs375428571 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CD2AP | GRCh38.p7 | 6:47530388 | TCTGTGATCCTACCC[C/T]GACAAAACCATTTAT | 23607 |
rs375449300 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47541543 | TTTCTTATTTGGAGA[A/C]TCAATTATTTTATCT | 23607 |
rs375491685 | in-del | -/AT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47622450 | CTGGCTGCCCTCCCT[-/AT]GGATCCCTGTGGTGC | 23607 |
rs375500716 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47583992 | TACTTTTGTTTTCAG[C/T]TGCAATTCCGTAATG | 23607 |
rs375597093 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47480673 | GCTTAGAACACTGCC[A/T]GTGCTGGCGGTGGTG | 23607 |
rs375677577 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47503097 | ATTGTACTCTATATT[A/G]AGATATTCAAGAAAT | 23607 |
rs375693039 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47620680 | TCTACCCATCCACGA[A/G]CGTGGGATGTGTTTT | 23607 |
rs375697496 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47567293 | TTCTCATGAAGGCAG[C/G]GTATTCCAAAATCTG | 23607 |
rs375713771 | snp | A/G/T | 3.5661e-05 | 0.00422249 | intron-variant | CD2AP | GRCh38.p7 | 6:47599269 | GTCGTGTTTCATACT[A/G/T]GTGATTTTTGCGTGT | 23607 |
rs375731510 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47543185 | AAAGAAAAAGAAAAA[A/G]GAAAAAAAAGAAAAA | 23607 |
rs375872956 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47503008 | CTACAAAGGATATGC[A/C]TGTGATTGTTAAGAG | 23607 |
rs375894917 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47505011 | TGGCTGTGGCAGTTT[C/T]TTTTTTTTTTTTTTT | 23607 |
rs375912788 | in-del | -/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47581390 | TGCTTCCATAATTTT[-/C]GAATAATTGATCTTT | 23607 |
rs375919322 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47544112 | ATCTTCAAATAAATG[A/T]GTTTCATTTTTAGCT | 23607 |
rs375930045 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47484239 | ACTTCACTAACCTGA[C/G]ACCATGCTGTACTCA | 23607 |
rs375933591 | in-del | -/AGTG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47607258 | TTCTTGTGAATAGTG[-/AGTG]CTACAGTAAACATGG | 23607 |
rs375945475 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47596856 | TTTCCATAATGGCTG[G/T]GGGAATTTACATTCC | 23607 |
rs375967211 | in-del | -/TTTG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47582787 | TTTTTTTTGTTTTTT[-/TTTG]TTTTGTTTTTTTTTT | 23607 |
rs376056600 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47536391 | ATTAACATAAGGTTA[A/G]TAGTGTAAACACTGC | 23607 |
rs376204661 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47494256 | TGTAGGTGCCAGGGG[G/T]TTCACATTCCTGTAG | 23607 |
rs376206874 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47591510 | TTTAGGTAGTACATT[C/T]TTTCTCTAAGGCATC | 23607 |
rs376244286 | in-del | -/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47543173 | AAAAAAAAAAAAAAA[-/G]AAAAAGAAAAAAGAA | 23607 |
rs376259964 | in-del | -/CCCTTC | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497368 | TTCCCCTTCCCCTTC[-/CCCTTC]TCCTTCCCTGTCGCC | 23607 |
rs376265655 | snp | C/G | 0.000651428 | 0.0180358 | intron-variant | CD2AP | GRCh38.p7 | 6:47580951 | CCATTTTTTAAAATT[C/G]TAAAATGGTAAAATT | 23607 |
rs376280295 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47556402 | TTCTTTTTTTTTTTA[A/T]TTTTGTTTTTTGAGA | 23607 |
rs376321472 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47515136 | GTAGGTCTGGCAAAG[A/G]TATTAGATAATTTAT | 23607 |
rs376333136 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47540523 | ATAATAGCTATTTAG[A/T]TGTTTTTATCTAATG | 23607 |
rs376378519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47528586 | TTGTAAATAGTAGTT[C/T]ATTAAGTATTTTAGT | 23607 |
rs376397699 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47551075 | AAAGACTACAAATTG[G/T]GTGCAGTGTATACTC | 23607 |
rs376428342 | snp | A/G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47518957 | CCCTCCCTACACTCC[A/G/T]CCTCTTGGTGTTCCA | 23607 |
rs376478979 | snp | C/T | 0.000347639 | 0.0131795 | intron-variant | CD2AP | GRCh38.p7 | 6:47580838 | ATGAAACTGGTCAGC[C/T]GTTTCCACCATTATT | 23607 |
rs376487126 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47601787 | AAGTTGAAAACATAC[A/G]TGAAAAACTTATTGA | 23607 |
rs376527881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47592023 | TTTCTTTTATAGATA[C/T]GGGGGTATTGATTTG | 23607 |
rs376550473 | in-del | -/CATG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47607135 | GCAAATGACAGGATC[-/CATG]TCATTCTTTTTTGTG | 23607 |
rs376626036 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47542899 | CTCACGCCTGTAATC[C/T]TAGCACTTTGGGAGG | 23607 |
rs376631303 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47509034 | TCATTTCTAGCTTTT[A/G]ATTTAAGTCAGAGAT | 23607 |
rs376634391 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47518623 | ATGATATATGCCTCT[G/T]TGTGTGAACATATAT | 23607 |
rs376637277 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47512995 | ACACTAGTTAGCTTA[C/T]AGGTAATTAGTAGAG | 23607 |
rs376641256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47546235 | AGTTTCAGCAATAGA[A/G]TTGAACAAGCAGAAG | 23607 |
rs376658798 | in-del | -/TTT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47564864 | ATTATATAAKTKTTT[-/TTT]TCTTTTTTGCTTTCA | 23607 |
rs376659106 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47550098 | CTAAGACCTGAAACT[A/G]TAACAGTTCTTGAAG | 23607 |
rs376665990 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497708 | TGTGAGCTGCAACTG[C/T]ACCCGGACAATTATA | 23607 |
rs376672565 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47532061 | CCTGGGCAACAGAGT[C/G]AGACTCCTTCTCAAA | 23607 |
rs376709257 | snp | A/C | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626697 | GTAACAGAAGATACT[A/C]TTTTTTATGCTCCTT | 23607 |
rs376720376 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47598598 | GGAAAAAATGGCATT[C/T]ACAGCAACCTGGATG | 23607 |
rs376766953 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47510655 | TAAATAAATGGTTGA[A/G]TAAATAAACGGGAGA | 23607 |
rs376770508 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47499608 | TTACTTACCCTTTCT[C/T]CTGGTAGTTTTCCAG | 23607 |
rs376782287 | in-del | -/GAG | 0.00557542 | 0.0525036 | intron-variant | CD2AP | GRCh38.p7 | 6:47509147 | GGAATAGGGAGCCCT[-/GAG]GAGTGGGAAAGGGTA | 23607 |
rs376802543 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47581750 | CCACAGCTCTTCCAT[A/T]CTGCAGTACGGTAGA | 23607 |
rs376827559 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47493584 | TTCTCTTAGTTTTCC[A/G]GATGTGTGGTTTGGT | 23607 |
rs376855523 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47523714 | AGAAATACTTTATAC[A/G]GGTAATACTAGAAAA | 23607 |
rs376882070 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47607132 | TGTTGCAAATGACAG[C/G]ATCTCATTCTTTTTT | 23607 |
rs376891545 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47610368 | CATCCCTTGTCTTCA[A/G]ATTCCCTTCTAAAAA | 23607 |
rs376915545 | snp | C/T | | | utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47477844 | TCTAACTGCGAGTGC[C/T]AAGGAAGAGGCGAGG | 23607 |
rs376918951 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47496406 | ACTTTTTGCAGTTTA[A/G]TATTACAAACTTAAT | 23607 |
rs376931629 | snp | A/G/T | 4.99874e-05 | 0.00499916 | intron-variant | CD2AP | GRCh38.p7 | 6:47607897 | TTTCTTTGGTCTATT[A/G/T]TGTCTCTTGACTTCT | 23607 |
rs376992107 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47571142 | CCATGGATAGTTTCA[C/T]TTTAAAAATGCCTTT | 23607 |
rs377006635 | snp | A/G | 1.65162e-05 | 0.00287365 | missense | CD2AP | GRCh38.p7 | 6:47596019 | CCTCCACCACCTCCT[A/G]TAGCCAAGTAAGTTT | 23607 |
rs377044656 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47565205 | TGTGGTGAATTAATC[A/G]TCTATTCTGTTACTG | 23607 |
rs377058304 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47622534 | TGCTTCCTCTACCCC[C/T]CTTGTATTTTGCTTG | 23607 |
rs377085060 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47537050 | AGTGATTTTTCATGT[A/T]GTTAATTATTTTGAG | 23607 |
rs377091187 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47514007 | TCCTTGTGTACAGCT[A/T]GTTCAGGATATTTCT | 23607 |
rs377092196 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47531805 | CGGCCGGGCGTGGTG[G/T]CTCACGCTTGTAATC | 23607 |
rs377092939 | snp | A/C | 3.30164e-05 | 0.00406289 | missense | CD2AP | GRCh38.p7 | 6:47577062 | ACTAATGAAGATGAA[A/C]TTACTTTTAAAGAGG | 23607 |
rs377096139 | snp | A/C/G | 0.00016494 | 0.00908005 | missense | CD2AP | GRCh38.p7 | 6:47609303 | CTGAAAAAGGATCAC[A/C/G]GGTAAGTAGCCCTTC | 23607 |
rs377096892 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47533214 | CATAGGAGTGTTGAT[C/G]GTTGCAACAGAAAGT | 23607 |
rs377111331 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47587432 | TAGGTGATTAAACTC[A/T]CACTTTCTACTTTCT | 23607 |
rs377249077 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47562644 | GTATTGTTGCTGGAG[A/G]TGTAATGGATGTTAA | 23607 |
rs377262117 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47499951 | CCAGGCTGGTCTCGA[A/G]CTCCTGACCTCAGGT | 23607 |
rs377262722 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47600261 | TATCACATAAATCAA[A/C]GGAGAACTCTAAATT | 23607 |
rs377282321 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47513381 | TTATTGCCTATCTAT[A/G]TAGGTTCTAGTTATT | 23607 |
rs377308880 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47527574 | CCTGTGGACACAGTG[C/T]ACCATAATGAATGAA | 23607 |
rs377314879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47613076 | CATCTGTTCAAGTTC[A/G]ATCCACTTTTAATTC | 23607 |
rs377316668 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47590108 | AGATAATTAGGCATA[C/T]TGATAGATATGACAC | 23607 |
rs377338831 | snp | C/T | 5.12466e-05 | 0.00506169 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624274 | GGGATTCAGAAGCAA[C/T]GCTATGAACTTCAGC | 23607 |
rs377342045 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47618871 | CTTTTGTTGTGGGCA[C/G]AGTTTTACCCTGTAT | 23607 |
rs377343231 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | CD2AP | GRCh38.p7 | 6:47624133 | CATAGAGTAAAATAA[A/G]CTACTAAACTAAGGA | 23607 |
rs377352983 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47480579 | CTTCTCTGTGCTTCA[A/G]TTTCTCAATCTATAA | 23607 |
rs377368839 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47584526 | AATTCAAGGCCCTCC[-/A]GTAACTAACTGACCC | 23607 |
rs377418401 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47484468 | TTACTGAAAGCATAT[C/T]TACTAATTGTTTGCA | 23607 |
rs377474329 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47610987 | TTTTTTTTTTTTTTT[G/T]AATATAAAACATTTT | 23607 |
rs377489268 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47609054 | ATTGTTTTTCTTCTT[G/T]CTGTTAAAATCTTTC | 23607 |
rs377515196 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47602974 | TGTTGAATAAGGAAA[C/T]ACATTTGTTTTTCTT | 23607 |
rs377516149 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47582445 | ATATTATTTAATCTC[A/C]CTGCATGTGTTTGTC | 23607 |
rs377566971 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47602511 | TTATAGTAACATAGC[G/T]GTTATATTAAGAAAG | 23607 |
rs377574538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47557264 | CAAAAATTTTCTCCC[A/G]TTCTGTAGGTTGCCT | 23607 |
rs377580660 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520609 | TGCCTCTGGTGGGTG[A/G]TGGTTGGGGGCGAAA | 23607 |
rs377585666 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47618087 | ACTTTGGAAGGTCAA[A/G]GTGGGTGGATCACCT | 23607 |
rs377611057 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47566321 | ATATATATATATATA[C/T]ATACACATACACATA | 23607 |
rs377617521 | in-del | -/TGTGTGTGTG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47491272 | ATATGTGTGTGTGTA[-/TGTGTGTGTG]TGTGTGTGTGTGTGT | 23607 |
rs377658847 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47580466 | CCAAAACAAAACAAA[A/C]AAAAAAAAAAACGGT | 23607 |
rs377660794 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47542056 | TCTTGTATCTTACTC[A/G]TATTTCATTGTGTAA | 23607 |
rs377673516 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47615217 | TGTTTTAAACTGTGT[A/G]TTAGTTAGGCTTAGC | 23607 |
rs377675771 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47595656 | TTCCTCTCTACCATA[A/G]TAAACATTTTTTAAA | 23607 |
rs377688764 | in-del | -/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47502455 | TTTTGTAGAGACGGG[-/G]TTTTGTTGTGTTGCC | 23607 |
rs377711807 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47523266 | AAGGGAGAAAACCTT[A/G]CAGATATTGGAATAT | 23607 |
rs377712188 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47481342 | CATGTGGTGGTGTTT[G/T]TTTGTTTGTTTGTTT | 23607 |
rs377712736 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47499956 | CTGGTCTCGAACTCC[C/T]GACCTCAGGTGATCC | 23607 |
rs377722480 | snp | C/T | 0.000296946 | 0.0121813 | intron-variant | CD2AP | GRCh38.p7 | 6:47574015 | TGACAGGATGTCAAG[C/T]GTTTTGTGATTCTAG | 23607 |
rs377756180 | snp | A/G | 0.000153988 | 0.00877328 | missense | CD2AP | GRCh38.p7 | 6:47579449 | GAGTATTTCCAGACA[A/G]TTTTGCTGTCCAGAT | 23607 |
rs377761664 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47483488 | AACAAAATGAGACAG[C/G]GTCCAGATTTCTTAT | 23607 |
rs377765626 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47519320 | ATAAGGAATGAATTC[C/T]CTTTGAGAAGGAACC | 23607 |
rs386406956 | in-del | -/A | 0.499104 | 0.0211472 | intron-variant | CD2AP | GRCh38.p7 | 6:47549461 | TTTTACAATAGCTGC[-/A]AAAAAAAAAAAAAAA | 23607 |
rs386406957 | in-del | -/AA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47549479 | AAAAAAAAAAAAAAA[-/AA]TAAGATGCTTAGGAA | 23607 |
rs386406958 | in-del | -/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47555871 | AATGTTTGCAGCGTC[-/C]ATAGGTTGTTGTGAG | 23607 |
rs386406959 | in-del | -/TTT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47564863 | CATTATATAAGTGTT[-/TTT]TTCTTTTTTGCTTTC | 23607 |
rs386700885 | in-del | CCCTTCCTTTT/TCCC | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497334 | TCCTTTCCTTTCCTT[CCCTTCCTTTT/TCCC]TTCCCTTCCCTCCCC | 23607 |
rs386700886 | in-del | CTTCCCC/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497352 | CTTCCCTTCCCTCCC[CTTCCCC/T]TTCCCCTTCCCCTTC | 23607 |
rs386700887 | multinucleotide-polymorphism | GT/TC | | | intron-variant | CD2AP | GRCh38.p7 | 6:47524850 | AAACTTTCAAAGTAG[GT/TC]CTGCTATATCTGTCA | 23607 |
rs386700888 | multinucleotide-polymorphism | AA/GC | | | intron-variant | CD2AP | GRCh38.p7 | 6:47622094 | AATATGGCTGCCTAT[AA/GC]TGAATCATGCTGGTT | 23607 |
rs387906340 | in-del | CT/G | | | splice-acceptor-variant | CD2AP | GRCh38.p7 | 6:47576523 | TTTTTTTCTATTCTA[CT/G]CCCTTAATCCTACAG | 23607 |
rs397726688 | in-del | -/CA/CATATATATATATATA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47589566 | ACACACACACACACA[-/CA/CATATATATATATATA]TATATATATATATAT | 23607 |
rs397743504 | in-del | -/A | 0 | 0 | intron-variant | CD2AP | GRCh38.p7 | 6:47611389 | GGAAGAGGGGGGGAA[-/A]TAGGATTAAGGAAAG | 23607 |
rs397752693 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47555813 | GAATAATTTTTTTTT[-/T]TAACGTGAAAGGGCT | 23607 |
rs397777271 | in-del | -/GT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47499326 | TGTGTGTGTGTGTGT[-/GT]TGAATATATGTGTAT | 23607 |
rs397798049 | in-del | -/A | 0.375 | 0.216506 | intron-variant | CD2AP | GRCh38.p7 | 6:47570153 | CTGCACTGAAAGCTT[-/A]AAAAAAAAAAAGAAA | 23607 |
rs397827995 | in-del | -/C/T/TC | 0.00597247 | 0.0543191 | intron-variant | CD2AP | GRCh38.p7 | 6:47493366 | GTGTTTTTTTTTTTT[-/C/T/TC]CCAATGCTTTAAATA | 23607 |
rs397943993 | in-del | -/AGA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47504690 | GGGGTACCTTGGAGA[-/AGA]TACTGCAGGTTCAGT | 23607 |
rs397946267 | in-del | -/AT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47547499 | TCTATATATATATAT[-/AT]GCACCTAACACTGGA | 23607 |
rs398001456 | in-del | -/T | 0 | 0 | intron-variant | CD2AP | GRCh38.p7 | 6:47543172 | TCTTTTTTCTTTTTC[-/T]TTTTTTTTTTTTTTT | 23607 |
rs398001457 | in-del | -/A | 0 | 0 | intron-variant | CD2AP | GRCh38.p7 | 6:47555814 | CAGCCCTTTCACGTT[-/A]AAAAAAAAAATTATT | 23607 |
rs398001458 | in-del | -/TATATATATA | 0 | 0 | intron-variant | CD2AP | GRCh38.p7 | 6:47566305 | ATGTGTATATATATA[-/TATATATATA]TATTCTAATGAGCAG | 23607 |
rs398001459 | in-del | -/A | 0 | 0 | intron-variant | CD2AP | GRCh38.p7 | 6:47567097 | CAGCATAGTAAAGTT[-/A]AAAAAAAAAAAAACT | 23607 |
rs398001460 | in-del | -/A | 0 | 0 | intron-variant | CD2AP | GRCh38.p7 | 6:47570544 | GCCACTGGAAAGAAG[-/A]AAAGAGGATAAGGAG | 23607 |
rs398001461 | in-del | -/T | 0 | 0 | intron-variant | CD2AP | GRCh38.p7 | 6:47570617 | TATCACTGAGAACCA[-/T]TAAGTGACAGAGAGA | 23607 |
rs398001462 | in-del | -/A | 0 | 0 | intron-variant | CD2AP | GRCh38.p7 | 6:47606650 | AGAAAAAAAGAAAAG[-/A]AAAAAAACACTGAAT | 23607 |
rs398039926 | in-del | -/T | 0.5 | 0 | intron-variant | CD2AP | GRCh38.p7 | 6:47540025 | GGGCTAATTTTTGTA[-/T]TTTTTTTTTTTGTAG | 23607 |
rs398048500 | in-del | -/T | 0.5 | 0 | intron-variant | CD2AP | GRCh38.p7 | 6:47513159 | TTTTTTTTTTTTTTT[-/T]CTTCTTTTAAAGTAA | 23607 |
rs398048501 | in-del | -/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520752 | TTTTTTTTTTTTTTT[-/T]GTCCCTGTGGTGTTT | 23607 |
rs398048502 | in-del | -/T/TC | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47613520 | TCCTTTTTTTTTTTT[-/T/TC]CCTGAGCAGTAGGTC | 23607 |
rs398065770 | in-del | -/AAAAAA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47551188 | AACCTATGGAAATAA[-/AAAAAA]GAAAAAAAAATTTAA | 23607 |
rs527243987 | snp | A/C | 1.64912e-05 | 0.00287147 | missense | CD2AP | GRCh38.p7 | 6:47554654 | TTTTCAGGTAGAAGA[A/C]GGCTGGTGGAGTGGA | 23607 |
rs527284449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47510634 | ATACATGAGTCCATA[C/T]TGATATAAATAAATG | 23607 |
rs527287458 | snp | C/T | | | downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47627611 | TCAAAGGGGAGCTGC[C/T]ACCATCTTACAGATT | 23607 |
rs527297900 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47561920 | CAAGTAGGCGCCCAC[C/T]ACCACACCCAGCTAA | 23607 |
rs527313863 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47495843 | TTTTATGCTTTTTCT[A/G]TTATTTTAGTGATCA | 23607 |
rs527335394 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47604266 | TAAAAGCATTTAGAT[A/T]TGTCATGAGTCCAAA | 23607 |
rs527346931 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47623916 | GACTGATTTTTTTAC[A/G]GCTTTAATTTTAAAT | 23607 |
rs527361028 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47608282 | TAGATCTCTGCATCT[A/G]TTTCGTTTCTCCATT | 23607 |
rs527377228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47547231 | GTAAATGGCCTAAAT[A/G]CTCCATTTGACATAT | 23607 |
rs527397078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47597529 | CACTTGAGCAGGAGA[C/T]TGAACATCTTAGTGA | 23607 |
rs527482811 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | CD2AP | GRCh38.p7 | 6:47575694 | TGTTTCTGGGTTAAA[G/T]TACTGTTAAATAATA | 23607 |
rs527521534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47530955 | TAACATATAACTGAA[C/T]GTTATTTTAAAATTT | 23607 |
rs527567338 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47510801 | TAGATGGGGCCGGGC[A/G]CGGTGGCTCATGCCT | 23607 |
rs527573848 | snp | A/G | 1.6788e-05 | 0.00289719 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47624218 | GAAAAAAGCTGTCCT[A/G]TCTTCTTGAGTGGTG | 23607 |
rs527591950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47611923 | GCTATAGAAAAAAGG[A/G]CAACTATATAGAAAG | 23607 |
rs527598582 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47516762 | TGAAAAGTTAGAAAA[C/G]AGGACAGTGGAGGCT | 23607 |
rs527604838 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47620069 | AAGCTCTTTAATTAG[G/T]TCTCAGCTATTTATC | 23607 |
rs527624395 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47485604 | GTAGTTAGCTTTAGT[A/G]TATGGTGTTTATAAA | 23607 |
rs527631909 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47509125 | TTTCAGTATCATTGT[A/G]TCTCAGGGAATAGGG | 23607 |
rs527657671 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47488948 | TATTTTGGGTGGATG[C/T]TTAGAACCATGGAGA | 23607 |
rs527672513 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47613378 | CTAAATGTCTCCTTG[A/G]TTCATGGGCTACAGA | 23607 |
rs527683059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47569682 | TATTCAGGTTCTGGA[A/G]TAGAAGAAAGTGCTC | 23607 |
rs527689872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47578094 | AAGAATTTTATAAAT[A/G]TATGTGAATTTTCAT | 23607 |
rs527713179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47621250 | TGAGAGTTTTAATCA[C/T]AAAGGGATGCTGGAT | 23607 |
rs527769475 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47486568 | AGTGATGATATACTG[A/C]GTACTGGCAGTAGTT | 23607 |
rs527805362 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47511738 | GCTTTATCACTTCAG[A/T]TGTGTATGTTAAAAT | 23607 |
rs527821829 | in-del | -/GTTTAAGAAATCTGGATGGAG | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47483252 | GGCGACAGAACAGTA[-/GTTTAAGAAATCTGGATGGAG]GTCTATATGTGCCTA | 23607 |
rs527822178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47563078 | GAATAGTTTGAACTC[C/T]GCTATAATTTTTAGA | 23607 |
rs527826064 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47516693 | AATTTTCCCATTTAT[A/G]TACTTCCCATTTTTT | 23607 |
rs527835727 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47546415 | GAAATCTAAAAGTTT[-/A]AAAAAAAAAATTGGG | 23607 |
rs527846710 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47488203 | GTTTGGCAGAGAGAG[A/T]CATTTCTGTATGAGT | 23607 |
rs527858856 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47489208 | GTCTCGCTCTTGTCC[C/T]CCAGGCTGGAGTGCA | 23607 |
rs527875957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47591419 | TCAGTGAGATAAATA[C/T]GAATAAATATATTTT | 23607 |
rs527955338 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47577327 | TTGTAATTTACATAT[G/T]GGGAATTATTGTTAA | 23607 |
rs527973870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47496398 | TGTCTTTCACTTTTT[A/G]CAGTTTAATATTACA | 23607 |
rs527989987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47532621 | ATTTATCAGTACTGT[C/T]TTTATGCCAGTAGCA | 23607 |
rs528018610 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47584560 | GATTACATTTTTGAT[A/C]TCATCTTCCACCCTT | 23607 |
rs528018826 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47573768 | TGCTGGGATTACAGA[C/T]GTGAGCCACCACAAC | 23607 |
rs528044279 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47556364 | CCAGCTTCATTCATG[A/T]CCCTCCAAAGGACAT | 23607 |
rs528047162 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47522644 | CCCAGTAAGTTTTTC[A/G]GGAAGCTGACAAATG | 23607 |
rs528053098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47617223 | TCCCACTTTGGCCTC[C/T]CAAAGTGGTAGGATT | 23607 |
rs528069281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47529539 | CTGGAAACCCTGAAC[C/T]GGAATAGGTGCATAA | 23607 |
rs528070631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521591 | CTGTTTTTAAGCTGT[C/T]GTTATTAAGCTAGTG | 23607 |
rs528077821 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47573532 | CTTGCCCTGTCGCCC[A/C]GGCTGGAGTGCAGTG | 23607 |
rs528092222 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47581041 | TATATGAAAATTGAG[A/T]GTTCACATGCATTAG | 23607 |
rs528150570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47566773 | TCCAGCGTCATCCAT[A/G]TCCCTGCAGAGGATA | 23607 |
rs528156578 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47526306 | GAGTTCCAGAGAAGA[A/T]GGTGGTGGACCTCAC | 23607 |
rs528209167 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47522208 | GTGAATTTTGCAAGC[A/G]CCAGAGCACAGAGAG | 23607 |
rs528211048 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47566320 | TATATATATATATAT[A/G]TATACACATACACAT | 23607 |
rs528212824 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47573977 | CTGTGTTTTATTAGA[A/C]GGCATATAGAATGTA | 23607 |
rs528237271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47544227 | ATTTTAAGTAGTATT[C/T]CCAGACTTGATTAGG | 23607 |
rs528314320 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47508568 | TTTTTTTTTTTGGGA[C/T]GGAGTCTCGCTCTGT | 23607 |
rs528319289 | snp | C/T | 0 | 0 | intron-variant | CD2AP | GRCh38.p7 | 6:47483891 | CCTCAGCATATCCTT[C/T]TGTTTCAGAAACAAG | 23607 |
rs528338347 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47580313 | GTATATCAATATTTT[A/C]AGGTATTAAGTCTTA | 23607 |
rs528365821 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47595577 | ACTACACTTAAAAGC[A/C]AAGCTTCCTGGGAAC | 23607 |
rs528371536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47535808 | ATTTTTAGGCCCACG[A/G]GAGGTTTTTTCATGA | 23607 |
rs528384356 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47499807 | GACCTCGGCTCACTG[C/T]AACTTTCGCCTCCCG | 23607 |
rs528392909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47491216 | TAAGAAATACTTAGC[C/T]CTGGGAATAAAAAGT | 23607 |
rs528404870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47587714 | GAATGCAAGTAGGGA[A/G]GCATGTAAATGTGTA | 23607 |
rs528426663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47485739 | ACACCCTATGTAGGT[A/G]TACCATTTTTATTAC | 23607 |
rs528429558 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47552367 | CTTCCTCATAGCTTA[C/G]CTCCCACATATGAGT | 23607 |
rs528448995 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47553390 | CTCACTATGTTGCCC[A/G]GGATGGAGAGCAGTG | 23607 |
rs528471222 | in-del | -/AAGAT | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47599610 | TAGAAATAATAAAAG[-/AAGAT]AAGTAAAATTTTTAT | 23607 |
rs528486264 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47478081 | AGAGACTGGTAGGAG[A/G]GCGCCGCGGGCGGAT | 23607 |
rs528525965 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47571024 | AACCCCCTTCCCTGC[C/T]TTTTTTTTTGTTTTA | 23607 |
rs528531491 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47545704 | ACGGGACTCTGTGCA[G/T]ACAACCCCCAGTACC | 23607 |
rs528544365 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47514722 | ATGATAGGTGTTACA[A/G]AATCTTTGAAAAAAT | 23607 |
rs528545988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47575074 | CCTTTCCTAACTTGC[C/T]ACGTATTTTCTTATG | 23607 |
rs528549240 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CD2AP | GRCh38.p7 | 6:47582945 | CCGCCACCACGCCCG[A/G]CTAATTTTTTGTATT | 23607 |
rs528576485 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625536 | CATCTAAAACACAAG[G/T]GGGTTTATTTAAATT | 23607 |
rs528581614 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47494194 | TTAGTGTGAGGATTT[A/T]TATTTATCTGCCTAG | 23607 |
rs528598909 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47538123 | TATTCATGTAATGAA[A/T]ATTTCATTACATGAA | 23607 |
rs528629937 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47612823 | GATTGAACTCATAGA[C/G]ATAGAGAACAGAAGG | 23607 |
rs528639131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47551998 | TGGTTACAAGTGAGT[C/T]GTAAGCCATCAAGAT | 23607 |
rs528649235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47500847 | CGCCTCCCGGATTCA[C/T]GCCATTTCTCCTGCC | 23607 |
rs528655641 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CD2AP | GRCh38.p7 | 6:47602729 | ACCGTGTCTCTACAG[A/G]AAAAAAAAAAAAAGC | 23607 |
rs528692374 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47559113 | TAGTTTATTTGCGTA[C/G]AGGTGTTTATAGTAT | 23607 |
rs528694873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47493348 | GATACAGATTTCTAG[A/G]TTGGTGTTTTTTTTT | 23607 |
rs528772625 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47595434 | TTTAAATTTGAATGT[A/T]ATATAGGACTTGAGT | 23607 |
rs528777744 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47498115 | CCTCTGTTTTGGTTC[A/G]TATTTTAATTTTGCT | 23607 |
rs528781424 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47552801 | GCTTCTTTAAGTCTG[A/G]TAAAAATTCTGGTCA | 23607 |
rs528795742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47603262 | ATTTTAAAGATAGTA[C/T]TGAGTCATATTTTTA | 23607 |
rs528827618 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47507178 | CACAAGGTTGCAATA[A/G]TTCAGTCACATCTTT | 23607 |
rs528857291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47541469 | AAAACTACAATAAAA[A/G]ATCAGATACAAATTA | 23607 |
rs528882367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47489541 | AGTTCTTACATAGCA[A/G]CTTCCCATTTTTTGG | 23607 |
rs528882658 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47585416 | TAAACAACTGGAAAA[-/T]TGGACAAAATGTATG | 23607 |
rs528905829 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47481280 | TTAGATAAGGCGGTG[A/C]ACTTTTTAGTTTATT | 23607 |
rs528924683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47548902 | GGATAGTTTAACATA[C/T]GCAAGTCAGTAAATA | 23607 |
rs528936229 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47495733 | CTTGTAAGGGTGGGA[A/G]TGATGACTTTAAAGC | 23607 |
rs528937952 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47508094 | ATATGCAATGACTTC[C/T]ACTTAAATTACCAGC | 23607 |
rs528947647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47586028 | GTCTGATTAAAGATT[A/G]CCAGGCATAGAAAGA | 23607 |
rs528962173 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47578276 | TGTGATCATAGCTCA[A/G]TGCAGCCTTGAGCTC | 23607 |
rs528984115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47592581 | TGTTATTTATAACAA[A/G]CATCTTTCAACCACG | 23607 |
rs528998080 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47542456 | AATTTAATTTCCATT[G/T]TGGTGATATTAATAG | 23607 |
rs529032199 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47605976 | TATCAGGTAAAGAGG[A/G]TTTTTTTTTTTCTTT | 23607 |
rs529036600 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47555539 | TAACCTTAAGGTTGC[C/G]AGTATCATTGGTTTT | 23607 |
rs529057385 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47613962 | AAACCACATGAACCA[G/T]CCTCTGCTACCTTCA | 23607 |
rs529076440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47511608 | TGTGGGAACTTTCTA[C/T]TTCCTTTGTAACTCT | 23607 |
rs529083969 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47592338 | CCCCACACTGTAAGC[-/A]AAAAGTAACTGAAAA | 23607 |
rs529129045 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47613198 | TCCAAAATATTGACA[G/T]TTTGACTTTCTCTTA | 23607 |
rs529133894 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47602179 | TATATAAATGCAGAC[C/T]GACTTTTGTACATGT | 23607 |
rs529164860 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47556422 | GTTTTTTGAGACAAA[A/G]TTTAACTCTTGTTGC | 23607 |
rs529169411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47606439 | TAGAGGGAGAGAGGT[A/G]TGTTCATTCCAACAG | 23607 |
rs529185529 | in-del | -/G | 0.00438332 | 0.0466095 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625825 | TTACATTAGGGGTTT[-/G]GGGGAATGCTAATTA | 23607 |
rs529190637 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47548037 | CAGTGCTAAGAGGAA[A/G]GTTAATAACCTAACT | 23607 |
rs529214179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47504095 | GAAAACAATCTTTAG[A/G]GCTCTTATCAATTAC | 23607 |
rs529223277 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47557668 | TCTGAGGCCTCTGTT[C/T]TGTTCCATTGGTCTA | 23607 |
rs529239937 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47513585 | TTTAAGACTGCACAT[A/G]CAGTATTATAGGAGA | 23607 |
rs529250935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47608210 | CAAATGTTTTTGAAA[A/G]AGCTTACATTTTAAT | 23607 |
rs529278982 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47506728 | GAGGTTGCAGTGAGC[C/G]GAGATGGCAGCAGTA | 23607 |
rs529280412 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47519732 | GGAGAAATTGGAGAA[G/T]AAAATCACCTAAATT | 23607 |
rs529311181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47616017 | CTTGAACTCCTGACC[C/T]TGTGATTCGCCCGCC | 23607 |
rs529327157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47607635 | TTCTACATTGCCTGG[A/G]GTACTGGTGGTACTG | 23607 |
rs529329622 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47565254 | GTCCAAGATAAATTT[A/C]TTTTAGTATTCAGTC | 23607 |
rs529335243 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47550270 | AGCAGAGTAAACAGA[A/C]CACAGAGTGGGAGAA | 23607 |
rs529360639 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47601587 | GGAAGTCAGTAGTGT[A/C]TGTCGTAAGCATTAA | 23607 |
rs529362654 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47593805 | AGCAGTTCCAAACGT[C/G/T]CAAGAGAATTGACAA | 23607 |
rs529372280 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47538648 | TGGAACCAAAAATTG[G/T]GTCAAAAATCCTTTT | 23607 |
rs529406647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47622363 | GGCCTGGAGGTCTCT[C/T]GCCCCGTTCAAATTG | 23607 |
rs529424501 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47600915 | CACAAATTTGGGGGA[A/T]CTTTATCACATAAGT | 23607 |
rs529434973 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47569437 | AAGGAGTAATGTTAC[A/G]AATAAGTTGCAAAGT | 23607 |
rs529499047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47512789 | CCTTTGCAGGACCAC[C/T]TGTGTTCTTAAGTTG | 23607 |
rs529500778 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47534170 | GTGGTTGGCCTTGCA[A/C]ATTACCTTGTAAGGA | 23607 |
rs529534207 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47526620 | ATCATGTTAACATTG[G/T]TTTACAGCAAATGAA | 23607 |
rs529565733 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47564668 | TAAATTTTAGGCAAG[G/T]TTCTGCATATTGTTG | 23607 |
rs529594490 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47615399 | AGAAAAATTTAATTG[G/T]CTCATGGTTCTACAG | 23607 |
rs529597499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47572268 | CTCATGCCTGCGCCC[A/G]GATCCACTGCGATGG | 23607 |
rs529646186 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47509376 | TAAAGGGAGCCCATG[A/C]CGTTGGAAAAATGGC | 23607 |
rs529672041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47611768 | TTCCTTCCACTCCTT[C/T]TGTCCCCAGAATAAT | 23607 |
rs529680876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47560480 | TAGTCTTCTAGCCTT[C/T]TTCTGTTTTTTGTTT | 23607 |
rs529700389 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47538830 | TCAGACATGAAATAC[C/G]TAACTATTCTTGATG | 23607 |
rs529731944 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47553755 | TATTAAAAATTTCAT[A/C]GAAATTGAGTAATCT | 23607 |
rs529738645 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47601444 | ATACTTAGGCCCTGT[A/G]AAGTTCAGAAAATAC | 23607 |
rs529764091 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47496641 | TTCCTGCACGTGATA[C/T]ACAAATATAAAAAAT | 23607 |
rs529768718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47596822 | ATCTTTTTAATTTCT[C/T]GAGGGACCTTTGTAC | 23607 |
rs529770434 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47604745 | GCCTTCAGATTATAT[A/C]ATGCATTTTTCATTG | 23607 |
rs529781477 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47501204 | GCAGGCTGAGTAATA[C/T]AGCCAGACCCCATCT | 23607 |
rs529796012 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625310 | TTACCTAATAGACCA[A/G]ACTAACTCATGGAGA | 23607 |
rs529823140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47509869 | TTTTAGAGAAAATTT[A/G]TTGCAGTTATAGAAC | 23607 |
rs529849638 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47478033 | GGTGAGGAGCTGTCG[C/T]CGCCTTTGCCTCTGC | 23607 |
rs529853090 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47599975 | TAATCTGTACTTCCT[C/G]TTTTTTTTTTAATAC | 23607 |
rs529879147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47530113 | CCCGATTTGCCTTAA[C/T]ACCACTGAATTTATG | 23607 |
rs529881926 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47567914 | GGAGAGTGAATTGCA[A/G]TGTGGGGAGTAGATT | 23607 |
rs529924060 | in-del | -/CT | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47482838 | AGAGAATATCTTCCC[-/CT]GTTATTAAATATATT | 23607 |
rs529924896 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47581836 | GGGTAATAGTGGCAG[A/G]TCCAGGATTAGAAAT | 23607 |
rs529935560 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47477464 | TAACTCCGCGTCGCC[A/G]CCGCGGAAAGTGGGG | 23607 |
rs529952109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47523287 | ATTGGAATATTAAAT[A/G]GAAGACAAGTTTACT | 23607 |
rs529956218 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626233 | TTTTGCTTGTGTCCT[C/T]CTCAGTCAGAATAGA | 23607 |
rs529964627 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47618473 | ATCCATGTTTTTTTT[A/T]ATCTTTGCTCATAGC | 23607 |
rs529995302 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47480472 | CTTAAGTTTAGGTGG[C/T]ACAGCTAGAGAGTTA | 23607 |
rs529996332 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47550004 | GAATAATTGGCTAGC[C/G]ACATGCAGGAGAATG | 23607 |
rs530001571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47620280 | ATTCTCCTACATGCG[A/G]CTAGCCAATTATCCC | 23607 |
rs530002745 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47575566 | ATGGTGTTTAGAGTT[G/T]GGGAAAACTAAAGTA | 23607 |
rs530020939 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47513080 | GAGCTGTAATAAAGA[C/T]TGTAGGATTATGACT | 23607 |
rs530046552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47576436 | AGTACCATTAGGGAA[A/G]GCTGGGTAACTGTAA | 23607 |
rs530051361 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47584539 | CCAGTAACTAACTGA[A/C]CCCCCGATTACATTT | 23607 |
rs530152508 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47531873 | AGGTCAGGGGTTTGT[C/G]ACCAGCCTGGCCAAC | 23607 |
rs530163748 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47627638 | GATTCTACCTCCTTG[A/T]TCACCCCACCCAGGA | 23607 |
rs530168000 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47518003 | AAAATGTCAGTTTAT[A/C]CCCCTAGGTAGAATG | 23607 |
rs530181363 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47577275 | ATAAGTGCTCAGAAC[A/G]TTCTCTTTTTGAGCT | 23607 |
rs530183155 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47568962 | TCAGTCAAGGGAGGA[G/T]AGTTATTCAGGGAGG | 23607 |
rs530197129 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47547201 | GTGTCTCACATGTCA[A/T]TACTAATGTTGAGTG | 23607 |
rs530204569 | snp | A/G | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520285 | GTAAAAATATTTATA[A/G]CAGTCAATATTGGTT | 23607 |
rs530223584 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47589754 | ATGAAAAGAACTTTC[A/G]ATAGACTTTTGGGCT | 23607 |
rs530230860 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47525849 | TATTTTTTCTTGGCA[A/C]GTTTTGTATTGACAT | 23607 |
rs530231846 | snp | C/T | 0.000199041 | 0.00997402 | intron-variant | CD2AP | GRCh38.p7 | 6:47503270 | ATTTCGTTTTTTCCC[C/T]CTTTTTTAGTTGACT | 23607 |
rs530257223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47546640 | AACTTCCCCGGCCTT[A/G]CCAGAGACCTAGACA | 23607 |
rs530277365 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47598454 | ATAACTTGCACATGC[A/G]TGTTTATAGCAGCAC | 23607 |
rs530299570 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47512152 | AACAGAGCGAGACTC[C/T]GTCTGAAAAAAAAAA | 23607 |
rs530312517 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47548861 | TAATACACCACGATC[A/G]AGTGGGTTTCATATC | 23607 |
rs530392260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47583979 | TGTAGTGGTATTTTA[C/T]TTTTGTTTTCAGTTG | 23607 |
rs530398331 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47517094 | AATTCTCACCCAGTT[C/T]ACTTGGGATCTGGCT | 23607 |
rs530428047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47539157 | ATAGAGATGATAGTC[A/G]TAATTTTCTTGTAGG | 23607 |
rs530435819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47579701 | CTTTCTCGACTGTAC[C/T]GAAAAATAACCTTAG | 23607 |
rs530462542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47581013 | GTATGATGTCTGTAA[A/G]CATTTTTAGAAATAT | 23607 |
rs530465149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47534878 | CAGCTCACTGCGGCC[C/T]TGACCTCCCAGGCTC | 23607 |
rs530472104 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47546611 | AAAAACATATTTGGG[A/G]GAATAATCAGAAAAA | 23607 |
rs530496582 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47528029 | GTGGTGTTGTAAAAT[A/T]GGTTTGTTTTATTCA | 23607 |
rs530507781 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47526525 | GATTTATTATATCTA[A/G]TATTCTTAGATATGA | 23607 |
rs530534489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47587587 | CCACTTTGAAGCACA[A/G]GTTATCCTGCTTTTT | 23607 |
rs530538608 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47501536 | ACAGAATTAAGGTTC[C/T]ATGAGAAAGGAAGGA | 23607 |
rs530539247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47623462 | ACAAGTCCTGTGTCA[C/T]TTGTTAGTGTGGAAC | 23607 |
rs530540712 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476352 | ATTTTCCTTTAAATT[C/T]TCAAGCATTTGACCC | 23607 |
rs530566286 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47556782 | TAGTGCTGCATTAAA[C/G]ATATGTGTGTGTGTG | 23607 |
rs530568209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47580246 | ATGTTTGTACATTAC[A/G]GCTTATCAATTATTC | 23607 |
rs530582293 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47585662 | GTGGTGGGAACTGCA[C/T]AGCGAGTACTCAGAT | 23607 |
rs530619949 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47548601 | GATCCAGGACCAGAC[A/G]AATTCACACCAGAAT | 23607 |
rs530638988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47528879 | ATTGTTGACTTTTAA[C/T]ATTTCTTTGTATATC | 23607 |
rs530645879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47491056 | ACTAATGGATCTGGT[A/G]CCTAACTTTAGAGGA | 23607 |
rs530648393 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47557534 | GGTCCAGTTTCAGTT[G/T]TCTGTATACAGCTAG | 23607 |
rs530678091 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47572375 | AATGCATATTTAAAA[C/T]GGGTTCATTTTATTC | 23607 |
rs530687988 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47499123 | CTTTCTGGCACAACA[A/G]AATGTTCCAGGCTAA | 23607 |
rs530697326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47489791 | CTCATTTTAAAACTC[A/G]TCCTCTTAATTATAT | 23607 |
rs530697338 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47528568 | CTTTGCTGTTTTTAC[C/G]AGTTGTAAATAGTAG | 23607 |
rs530697467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47542685 | GAGAAGTAAATTTAT[A/G]CTATCTTCATTACCT | 23607 |
rs530718855 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47543526 | TAGAAGTCCAAGATC[A/C]AGATACTGTCAGGGT | 23607 |
rs530731571 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47507185 | TTGCAATAATTCAGT[C/T]ACATCTTTATGCTTC | 23607 |
rs530776725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47493255 | CATGTCTTTTGTGTT[A/G]GGTCTGTTGGCAATG | 23607 |
rs530778469 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47593633 | TGAGATGGTTAAAAA[G/T]TTTTTTAAGAAAGGA | 23607 |
rs530806455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47595338 | TACAAATATAAGCCT[A/G]TAATTCTCTCGTCTG | 23607 |
rs530827719 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47498548 | TCTGTTAATTGGATG[A/T]TGGATTGATTGGGCC | 23607 |
rs530887726 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47572696 | TTCAAAAATTGACTT[G/T]GTTACTGACTACCTG | 23607 |
rs530894020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47545188 | TGCAGCTCCCACTGG[A/G]ATAGACAGAGCAGCA | 23607 |
rs530912858 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47536603 | GGATAGTAATGAAGC[C/T]GTGAAAACTTTTGCT | 23607 |
rs530961119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47558687 | TGACTTGATTGTGGT[A/G]GATAAGCTTTTTAAT | 23607 |
rs530990930 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47609102 | TAAATAAAATCAGAA[A/T]TTTTTTTTTTACGTT | 23607 |
rs531002014 | snp | A/T | 0.0883596 | 0.190715 | intron-variant | CD2AP | GRCh38.p7 | 6:47615796 | TAATTTAATTTAATT[A/T]ATTTATTTATTTATT | 23607 |
rs531013603 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47551702 | TTCAGATGGGGTATA[G/T]CCCAAATGGCTTGTG | 23607 |
rs531030124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47545659 | AGGTGCTGGTATCCA[C/T]GGCTAAGAGACCCAC | 23607 |
rs531043000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47617054 | CTCACTGCAACCTCA[A/G]ACTCCTGGGATCAAG | 23607 |
rs531068371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47595837 | TTTGATTGTTAATAA[C/T]TTGTGAAATATTTTA | 23607 |
rs531077074 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47512459 | ACTAATTCAGATAGC[A/T]ATACTGAAGAACAAT | 23607 |
rs531127994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47617779 | AAGAGCTTTCCATTA[C/T]ATGCTGAATAAAGTT | 23607 |
rs531160991 | in-del | -/CATC | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47621794 | ATTTTTCCAGAAATT[-/CATC]CATCCATCTCTTCTA | 23607 |
rs531173654 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47496512 | ATTTTCTTTGAGTCA[A/G]TGAACTTCTTAATTA | 23607 |
rs531198196 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47508423 | GCAACTTCCTGACCT[A/C]TCTGTATTCAGTGAG | 23607 |
rs531235322 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | CD2AP | GRCh38.p7 | 6:47497352 | CTTCCCTTCCCTCCC[C/T]TTCCCCTTCCCCTTC | 23607 |
rs531260428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47514926 | GAGTGGTGGCACGCA[C/T]CTGCAATCCCAGCTA | 23607 |
rs531281104 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47591961 | TCCAGAGTAGCTGGG[A/G]CTAAAGGTACATGTC | 23607 |
rs531296308 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47479696 | GTTCTTTTCTGTCTT[A/G]AATGGGATGCAGAAT | 23607 |
rs531301631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47548840 | TCCAACAACATATCA[A/G]AAAGATAATACACCA | 23607 |
rs531343182 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47599105 | TAATAATTTTCTACA[C/G]TTAACTAAACTGTTC | 23607 |
rs531365240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47555487 | TTATTTGGCAATTTT[A/G]TGATTAGTTGGATTT | 23607 |
rs531397418 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47620957 | GAAGGAGTCTTGAGG[G/T]TTTTCAAGGTAAATG | 23607 |
rs531408962 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47584611 | CTCACTCTCTAGTCC[A/C]TAAATATGTCATGTA | 23607 |
rs531440792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47540073 | CTGTGGTCCCAGCTA[C/T]TTGAGAGGCTGAGGT | 23607 |
rs531467367 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47591521 | CATTTTTTCTCTAAG[C/G]CATCTCCAAGTGATC | 23607 |
rs531482659 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47505611 | ACGGGGCGGCTGGCC[A/G]GGCGGGGGGGGCTGA | 23607 |
rs531523115 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47604965 | CGAACAGTGATGCCT[G/T]TTTTTCTGCCTTACC | 23607 |
rs531532261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47517942 | ATTTAATGTGTTGTG[A/G]TCAGCATTTTACATA | 23607 |
rs531563121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47620165 | AAGGGTTTTTCTGTT[A/G]TTATCTTCAAGAATT | 23607 |
rs531585048 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47525005 | ATTTAATTTAATCAT[A/C]ATAAAAAGGAAAATC | 23607 |
rs531586820 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47492163 | AATTTCTATCATAAT[A/C]CCTTCAAGCTGCTAT | 23607 |
rs531589879 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47615161 | TGGGGACTTGCAGTT[G/T]GAAAACCTTGGCTCT | 23607 |
rs531593561 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47519761 | TTATAAAATTAGTCA[A/G]CAAATTTTTTTGAAT | 23607 |
rs531638404 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47622333 | AACCAGATTTGCCGC[A/C]CTACCCAGAGTTGTG | 23607 |
rs531684702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47557010 | TGACTTTTTAATGAT[C/T]GCCATTCTAACTGGC | 23607 |
rs531738143 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47512638 | AAAGTATTTTACAAA[G/T]GATATTGAACACAAG | 23607 |
rs531779694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47519174 | AATAAGATAAAGTTA[A/G]TTTTTGATAGCCATA | 23607 |
rs531784655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47614160 | TTTCTTATTATTCAT[A/G]TGTTCACTGCAGTAG | 23607 |
rs531870858 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47539691 | GAGTGTTAATGCTTT[A/G]TTGTGTGGGAGATGT | 23607 |
rs531892748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47526574 | TGAAGGTTCCTAAAA[C/T]GGTTCTAGATCTTGA | 23607 |
rs531903439 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47488936 | TTTGTACGTGTTTAT[A/T]TTGGGTGGATGCTTA | 23607 |
rs531948525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47585228 | GAATGGCGTGAACTC[A/G]GGAGGCGGAGCTTGC | 23607 |
rs531967845 | in-del | -/T | 0.078151 | 0.181571 | intron-variant | CD2AP | GRCh38.p7 | 6:47482381 | TTTGTTTTTTTTGTC[-/T]TTTTTTTTTTTTTTT | 23607 |
rs532025395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47578960 | CCGTACCCGGCCTCA[C/T]TTTATCTTTCTCTTT | 23607 |
rs532030361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47566911 | GATATTGTAAATAGT[A/G]CTGTAAATATTGTAA | 23607 |
rs532049779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47621910 | CCGTAGAACTCCCAA[A/G]ATTATATGCCCTTAG | 23607 |
rs532059732 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47596671 | TCATCCATTGATACT[G/T]TAGGTTGCTTCCATA | 23607 |
rs532060148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47522281 | GAGAAGGTTAACAAA[A/G]TATTTTTATTCGCTG | 23607 |
rs532070178 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47603329 | TCTTCTTTGATACCA[C/T]AGAATTAAAATTGCT | 23607 |
rs532115808 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47523177 | TAATAGAACAATTCA[A/G]GAGCTAGCTTTATAA | 23607 |
rs532128791 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47609629 | TCTTGAGCCTGGGAA[G/T]TCAAGGCTGCAGTGA | 23607 |
rs532134340 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47580363 | AAATTGAGAAAAAAC[A/C]TGTCTTTGCCTTTAA | 23607 |
rs532138417 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47574920 | CTTCTATCAGTCCTA[C/T]CTCTTTAACTCTGAA | 23607 |
rs532160892 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625236 | TTTCAGAACTTCAGT[A/G]TGAGGTTTCCTATTT | 23607 |
rs532202959 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47509266 | AAAACAATTAAAATG[A/G]TAACATTAAAGATCA | 23607 |
rs532207103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47535876 | CACTCTAGGGAGCTA[C/T]AAAGGGATAAGTTTC | 23607 |
rs532209662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47535658 | ATACTGCTTTCTAGC[A/G]TTATTGCCTGAAGGT | 23607 |
rs532229799 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47477978 | GGTCGGGCGGGCGGG[A/G]TAGGGCCCTCCCGCC | 23607 |
rs532266757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47610437 | AAAAGTATAAAAGAA[C/T]AAAAAATAAAAATAA | 23607 |
rs532276391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47567503 | GCTTTTTTTTCCATT[A/G]GGAAAGAAAAGATGA | 23607 |
rs532289096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47484561 | ATACTGGCTTAAGAT[A/G]TTGTTCCAGTGTCAG | 23607 |
rs532306592 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47486284 | ACTTCTCACAACCCC[G/T]GGGTTCTGACATAAA | 23607 |
rs532321007 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624516 | AAGAATGTGCACAGT[A/C]GTTTTTTTATTGAAA | 23607 |
rs532324296 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47601636 | CTTTTTAAATTAGAC[A/G]ATCATATGTTCCTAG | 23607 |
rs532328197 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47478720 | AGATAAATTTGTTCA[A/C]AAACTTTTTTTTTTT | 23607 |
rs532355078 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47580456 | TTTTTAAAAACCAAA[A/C]CAAAACAAACAAAAA | 23607 |
rs532358420 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47487265 | ATGCGTGTCAAATGG[A/T]AATAAAAGGCTGTGT | 23607 |
rs532358424 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626458 | ATGAATTTTTTTTCT[A/T]CGTGTGAGTATAAAA | 23607 |
rs532363788 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47477396 | AGTGCGCTCGCCCTC[C/T]TTCTGTCCGCCTTTT | 23607 |
rs532369356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47545092 | AAATATTAATAAAAA[C/T]ACTTTCCTATATTTT | 23607 |
rs532378520 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47583072 | ACAGGTGTGAGCCTC[C/T]GTGCCTGGGCCAGTA | 23607 |
rs532386794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47479476 | TTCTCCACCTCCCTC[C/T]TTTCAGGTAACTTTC | 23607 |
rs532418864 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47592843 | ATTTGGCTGTTCTGA[G/T]CTGTATCCTTTATAA | 23607 |
rs532519744 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47531089 | ATGCTATCTCTACCC[A/C]AAAAAAAAATGTGTT | 23607 |
rs532542495 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47575789 | CTGTAGCTATAAGGA[A/C]CATAAGATTACCTGA | 23607 |
rs532558480 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47620677 | GATTCTACCCATCCA[C/T]GAGCGTGGGATGTGT | 23607 |
rs532568263 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47621361 | TATTGACTTGTGTAT[A/G]TTAAACCATCCCTGC | 23607 |
rs532570915 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47494974 | AGACAAGTCTGGGCA[A/G]TATAATGAGACCATG | 23607 |
rs532585825 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47552885 | CCATTTTTATTTTAG[C/G]TATACCTTCCATGAA | 23607 |
rs532623692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47576348 | GGTAGCTCTGAGCTA[C/T]GATTTAAGGAACTTT | 23607 |
rs532632702 | snp | A/C | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624546 | ACTTGTATTATTTTT[A/C]AAGAGATCTATACTA | 23607 |
rs532654729 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47627492 | ATGATAAAAATTAGA[C/T]GGATAAGGTTAAGAA | 23607 |
rs532659769 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47531834 | TCCCAGCACTTTGGG[A/T]GGTCGAGGCAGGCAG | 23607 |
rs532663634 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47524420 | GAAATTGTAAACACA[G/T]TAGCCCTCATTTTCT | 23607 |
rs532682135 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47587304 | CTCTGTTCTGTCAGA[G/T]ATGTGGGGCGCAGAA | 23607 |
rs532682879 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | CD2AP | GRCh38.p7 | 6:47601700 | TGATGTTAATACTTC[-/A]AAAAAAGTATTTTGG | 23607 |
rs532736076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47604012 | AAAAGTTTCCTGATT[C/T]GTTTAAAATATTCTT | 23607 |
rs532770526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47495111 | GAGGCTGCAGTGAGC[C/T]GAAATTACTCCATTG | 23607 |
rs532840602 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47531932 | ACAAAAATTAGCCAG[G/T]TGTGGTGGTGCATGC | 23607 |
rs532854337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47579590 | TTGAATAATTTTTAT[A/G]AAGGAGTTTCAGATG | 23607 |
rs532859789 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47501641 | TTTTTGGTGGTGGTG[C/G]TTGTGATTGTTGTTG | 23607 |
rs532871620 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47502047 | GGTTGGGTTCACATT[C/T]GGGGCTCTACTGGGG | 23607 |
rs532896890 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47490862 | AAGGGTGGGTTTTGT[G/T]TGCAGTTTGTTCACT | 23607 |
rs532915880 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47543397 | GAACCACCTAGGGAT[A/C]TTGTTAAAGTGCACA | 23607 |
rs532959271 | in-del | -/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47489972 | CTAAAGAGACTTTTT[-/G]TTTTTTTTTTTTTTT | 23607 |
rs532983065 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47563110 | TAAACGTGACCAAAG[A/G]AAGAAGTGGAAGCTA | 23607 |
rs532992233 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47492860 | GTTTTATATGATTCC[A/G]TTTTATGTCCTCTTT | 23607 |
rs532994692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47542553 | TGAAAGGGCAGGAGG[A/G]TATTAGCTTAGGCCC | 23607 |
rs533011405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47592607 | CCACGTCTGAGTTTA[C/T]ATTAATGAGGAGGCT | 23607 |
rs533012048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47498375 | AGAGCTTTCTAGGAT[C/T]GTTTATTGTTATTAT | 23607 |
rs533053356 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47527412 | AATAGGAGCAAAGAG[C/G/T]CATTACAAGGAGATC | 23607 |
rs533071081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47534742 | AGAATTACGGTGTTA[C/T]GGGAGCACATAGCAA | 23607 |
rs533078001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47579128 | GTTCCAGCCAGGCAC[A/G]GTGGCTCATGCCTGT | 23607 |
rs533090926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47600159 | CACTTTCTCATGTAT[A/G]TTCTTAGTTTAACTC | 23607 |
rs533091703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47592123 | TTAAAGGCATGAGCC[A/G]CTGCACCCAGCCTGT | 23607 |
rs533107945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47548981 | CAATAGATGCAGAAA[A/G]AACATTAGACAAAAT | 23607 |
rs533134728 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47550981 | AGTGGGAGCTAAGCT[A/G]TGAGGATGCAAAGGC | 23607 |
rs533143436 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47480514 | TCTGGACAGAGACTA[A/C]TTGAGGTCAAATTCT | 23607 |
rs533154214 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47512546 | TTATGAAAAACTTTA[C/G]ACACCATAAGTTTGT | 23607 |
rs533154595 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47505075 | CTTGGGTGTTTCTCA[C/T]AGAGGGGGATTTGGC | 23607 |
rs533165934 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47587942 | TTCCTTCTGAATTCT[A/G]TTATTGTAGGCTCAT | 23607 |
rs533172762 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47601650 | CGATCATATGTTCCT[A/G]GTATTAGTAATATAA | 23607 |
rs533218094 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47567476 | AGGCATGATTTACCC[A/C/T]CCTTGTTTGAAGCTT | 23607 |
rs533259604 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47541606 | ATGCTATTGGTTGCA[G/T]GTAGTGTGCTTCTTT | 23607 |
rs533295587 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47505553 | GTTGGGCACACCTCC[C/T]AGACGGGGTGGTGGC | 23607 |
rs533318090 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47535870 | TTCTTTCACTCTAGG[A/G]AGCTATAAAGGGATA | 23607 |
rs533339282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47616052 | CCTCCCAAAGTGCTG[A/G]AATTGCAGGCATGAG | 23607 |
rs533343224 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47621098 | GAAGAGGAGTGGTGA[C/G]AGCAGACATCCTTGT | 23607 |
rs533353200 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47618166 | TCTACTAAAAAATAT[A/G]AAAATTAGCTGGGCA | 23607 |
rs533367903 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47572319 | AATTGTTCTGTATCT[C/T]GTTGTATTTACATGG | 23607 |
rs533378729 | in-del | -/TTG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47566479 | AATCCTCTTGAGTTT[-/TTG]TTGTTGTTGTTGTTG | 23607 |
rs533382674 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47550334 | ACTATCCAGAATCTA[A/C]AATGAACTCCAACAA | 23607 |
rs533404854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47507308 | ATCTGTTTCTTCCAG[A/G]CTCCCATTAATGTTG | 23607 |
rs533408645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47609071 | TGTTAAAATCTTTCG[A/G]ACGTAAATATAATAT | 23607 |
rs533442711 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47504428 | AACATACAGTTGTCT[C/T]AGTATCCAGGAAACA | 23607 |
rs533467562 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47513649 | AGTATTCCATTGTCC[A/G]GCTAAGTATTACATA | 23607 |
rs533503109 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47602516 | GTAACATAGCTGTTA[C/T]ATTAAGAAAGCCCAA | 23607 |
rs533506527 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47537790 | TTTTTATTGCTAAGG[A/C]TGAGAATTTTTTTTT | 23607 |
rs533523389 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47495322 | ACGTCAAGATGGAGG[G/T]AGAGGTTGGAGTTAC | 23607 |
rs533557027 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47597403 | AGAAAAGCCAAGAAG[A/C]AGACAGCATAGAGGA | 23607 |
rs533563471 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47545943 | TAATATGACAAAACA[A/G]GGTTCTTTACCATTC | 23607 |
rs533569741 | in-del | -/TTG | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47499734 | TAGGAGTTAAGAGTT[-/TTG]TTGTTGTTGTTGTTG | 23607 |
rs533612077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47527952 | ATATATATTTGTGTC[A/G]TATTGTTGGCTAAGA | 23607 |
rs533619847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520193 | AGTTACTGAGACTGG[A/G]GATAAAGCAGACATC | 23607 |
rs533667236 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47582444 | CATATTATTTAATCT[C/T]ACTGCATGTGTTTGT | 23607 |
rs533699326 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521413 | AAAAATTAGCTGGGC[A/G]TGGTGGCGGGCGCCT | 23607 |
rs533712027 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47565310 | AAAGTGTTATGTTTC[G/T]GTTTTGTAATGTCTC | 23607 |
rs533719621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47508871 | GCAATAAGACTGTTT[C/T]ACTTTCTTATCATTG | 23607 |
rs533721609 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47516024 | AACTTTGTAAAATGC[A/G]TTTAATCATTGTGTT | 23607 |
rs533722873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47573252 | TAATTGAGTTTCCAT[C/T]GACTGCTTTGAAATT | 23607 |
rs533728152 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47600397 | TTAGATGTTTTTTAT[C/T]ACCTTATTATAAAAT | 23607 |
rs533728667 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47501122 | CTGGGCATGGTGGCT[C/T]ACGCCTGTGATCCTA | 23607 |
rs533740312 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47486298 | CTGGGTTCTGACATA[A/T]ATGCTTCTGCCTCTC | 23607 |
rs533746737 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47589436 | CACAAATATACACAC[A/G]TACACACACACAAAT | 23607 |
rs533750922 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47559855 | AGCATGAAGCAATAG[A/C]GCAAGTTCATAAAAA | 23607 |
rs533763390 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47618721 | TTAAATTTGTATATC[G/T]GACTTAATTTGCCAT | 23607 |
rs533803713 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47486775 | TGACTTTAAAAATGT[A/C]ATTCCTGGAGCATTT | 23607 |
rs533804071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47478363 | CCTGAGCGGCAGCAC[C/T]CCACCCTCTCCATTC | 23607 |
rs533804669 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47568057 | TATATAAGTGATAGC[A/G]CAAAGAACAGGACCT | 23607 |
rs533838003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47583385 | TATCATACAGAATAG[C/T]ATTACTACTCTAAAA | 23607 |
rs533888230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47589902 | CCTAACTCTGAGGAA[C/T]ACTGAAGTTCAACTT | 23607 |
rs533889174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47552623 | CAGTCTATTTTTGTG[C/T]ATTTTTTTACCACTG | 23607 |
rs533892852 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47494548 | TTTCCCTTGGAGTGT[A/T]GGCCTTTGTTACAGA | 23607 |
rs533900030 | in-del | -/AGG | 0.00517822 | 0.0506191 | utr-variant-5-prime, cds-indel | CD2AP | GRCh38.p7 | 6:47478076 | GCTGAAGAGACTGGT[-/AGG]AGAGCGCCGCGGGCG | 23607 |
rs533976187 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47611284 | GAAAAGCATACCAAA[C/G]CAGAAAATATATTAT | 23607 |
rs533997417 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47598696 | AATATGTGGGAGCTA[A/G]GCTGTGAGGACACAA | 23607 |
rs534011685 | in-del | -/TTT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47505034 | TTTTTTTTTTTTTTT[-/TTT]AATTTATTTTTTTAT | 23607 |
rs534016174 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47609490 | GAGACCAGCCTGGAC[A/G]ACATGACAAAACCCC | 23607 |
rs534039967 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47596024 | ACCACCTCCTATAGC[C/T]AAGTAAGTTTTACCT | 23607 |
rs534049618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47501859 | TAAAAGAGGTAAAAT[A/G]AATACATATTAATCT | 23607 |
rs534057906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47606038 | GAAAAGCACAGGTCA[A/G]TTTGTGAGTTCTTCA | 23607 |
rs534076442 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47482947 | GAAGTATAATGATTA[C/T]TCATTTGGGTGAGAA | 23607 |
rs534118541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47603477 | CACCAAGCCATCCTT[C/T]TGGAAACTGTCTTGG | 23607 |
rs534124306 | in-del | -/TC | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47611608 | TCTTCATGAATTTTT[-/TC]TTTTTTACTTTTTCA | 23607 |
rs534159210 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47531392 | TCTTAATCAGAATTA[A/T]TACTAATGAAATGTG | 23607 |
rs534185876 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47605300 | TTTACCTTTTGGGTT[A/C]TTGATTCATATATAG | 23607 |
rs534191133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47569103 | AGGAGGTTAGGCAGT[A/G]TAGAGAGTAAGTATA | 23607 |
rs534231766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47525310 | TACTAATTTTATATA[C/T]TTCTGGAAATCCTGA | 23607 |
rs534232474 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47510328 | CAGTGATACCTCAGT[A/C]GCCGTGAGTACATCC | 23607 |
rs534232786 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47612708 | AGATCCTGTCATTTG[A/C]AACAACATGGATGGA | 23607 |
rs534252256 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47539791 | ATTCTCTTCCTTGTT[A/G]GTAGCTTTACTTATA | 23607 |
rs534252363 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47568497 | CTGTAATCCCAGCCC[G/T]TTGGGAGGCTGAGGT | 23607 |
rs534285003 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47547599 | ACTTCAATACTCCAC[C/T]GACAGCATTAGACAG | 23607 |
rs534308618 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47503713 | TTAAAATAAATAATA[A/G]TTTTCATTTGGGTGG | 23607 |
rs534321823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47565486 | TTTCCACCCTTTTCT[A/G]AAAGTCTTCCACATT | 23607 |
rs534322555 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47598113 | TAGACAGTTCTCAAA[A/C]GAAGATATACAAATG | 23607 |
rs534348943 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47554837 | GTGTTTTATTTTGTA[A/T]TTTTTGAAACTCTGT | 23607 |
rs534365408 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47499442 | ATTACAAATCAGTAT[A/C]ACAGGATTGAAAGTA | 23607 |
rs534406098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47550626 | CTATGGAAAACAGTG[C/T]GGAGATTCATTTGAG | 23607 |
rs534438360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47507447 | GAAGAATCACTATCT[A/G]TGGCAGTGATAGCCT | 23607 |
rs534444098 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626795 | CATTTAAACTTGAAA[C/T]GTATGAGCAGAATGA | 23607 |
rs534466251 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47557957 | TTATTCCTATCCATT[A/T]GCATGGAATGTTTTT | 23607 |
rs534472133 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47500272 | TGATATAGAGATTGA[A/G]TAATTTCCCTGTTTT | 23607 |
rs534488999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47532237 | TAATCCCAGTACTTC[A/G]GGAGGCAGGGTGGAA | 23607 |
rs534536983 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47578787 | TCAGCCTCCTGAGTA[G/T]CTGGGACTACAGGCG | 23607 |
rs534568807 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47490917 | TATCTCTGTTGAAAA[A/C]CATGTAAGAAATGCT | 23607 |
rs534571313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47564904 | TGTCATATCCACTAT[A/G]TTTGATTATATCATA | 23607 |
rs534632027 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47571888 | GCTTCACACTAATGT[A/G]CAAATAACTTACCTG | 23607 |
rs534646640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521105 | ATATATTTAGCAGGA[A/G]GAATAGGGAAACACC | 23607 |
rs534650460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47513244 | GCTCTTAAATCCTGG[C/T]GCTCACTTTCACTGT | 23607 |
rs534650938 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624825 | GTGATGAAATAGGAG[C/T]TTCCTAGCTATATAA | 23607 |
rs534668582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47507962 | GGCTTAAATTACTCA[A/G]TAAACCATGCTGTAA | 23607 |
rs534680681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521975 | AGCCGAGATCATGCC[A/G]TTGCACTCTAGCCTG | 23607 |
rs534689232 | snp | C/T | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521322 | TTTGGGAGGTCGAGG[C/T]GGGCAGATCACCTCA | 23607 |
rs534728467 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47555359 | AGGAGAGTTTTTTTT[A/G]TTTTCCAAAAGAGGT | 23607 |
rs534735677 | snp | C/G/T | 0.00187798 | 0.0305858 | intron-variant | CD2AP | GRCh38.p7 | 6:47624163 | ATATTTTATGTTTGC[C/G/T]CAATTTATGTTTTTT | 23607 |
rs534741833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47529297 | TGTTGATGAAAAAAA[A/G]TTGGTTCCTAGCTGG | 23607 |
rs534752613 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47517696 | ATATTTCTTTATCAT[C/G]TTTTAGATCTTTTGA | 23607 |
rs534787804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47484923 | CATAGGGTGGTGGTC[C/T]CCTAAGATTATAATG | 23607 |
rs534806427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47618047 | TTAGTGGCCGGGCAC[A/G]GTGGCTCACACCTGT | 23607 |
rs534830238 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CD2AP | GRCh38.p7 | 6:47534726 | TATTAAACGTGTACA[A/G]AGAATTACGGTGTTA | 23607 |
rs534835503 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47546221 | AAAATGCTGTGGGAA[A/G]TTTCAGCAATAGAAT | 23607 |
rs534858682 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47492552 | CATCTTGCTATGTTG[A/C]CCAGGCTGGCCTTGA | 23607 |
rs534866348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47594710 | ACATCTTGAGGCCAT[A/G]TAAAAATAGATTTTT | 23607 |
rs534911158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47482463 | GGCTCACTGCAACCT[C/T]CGCCTCCCGGGTTCA | 23607 |
rs534922213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47528227 | TCACCCATGCTGGAG[C/T]GCAGTGCTGTGATCT | 23607 |
rs534930446 | snp | A/T | 0.0573587 | 0.15934 | intron-variant | CD2AP | GRCh38.p7 | 6:47615804 | TTTAATTTATTTATT[A/T]ATTTATTTATTTATT | 23607 |
rs534937805 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47588433 | ATATAATATGAAGGA[A/T]TCTTTAAAATCTGAA | 23607 |
rs534943996 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47579751 | TAAGAAGGGCTGTCT[A/C]TCCTAATAACATAAA | 23607 |
rs534952048 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47575134 | GAACTTCCACTTTCT[A/T]TCCTACATATTCCTA | 23607 |
rs534961105 | snp | C/G | 6.64673e-05 | 0.00576448 | intron-variant | CD2AP | GRCh38.p7 | 6:47580829 | ATATTTGATATGAAA[C/G]TGGTCAGCCGTTTCC | 23607 |
rs534974709 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47477579 | CGGGGGGAGAGCGAG[C/T]CCAAGCTCCTCTGCA | 23607 |
rs534988659 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47529800 | CAAAGACTTTAAGTG[G/T]GAATTTACTGTATTT | 23607 |
rs534992449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47491768 | AAAATTATGGATTTT[A/G]AGATTTTTAAGCTTG | 23607 |
rs535009896 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47581234 | AAATCCATTTGTTAA[C/T]GTCTCAAATAATAAT | 23607 |
rs535036861 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47586203 | AATGTGAACATTACA[A/G]TGCAAAAACTGGAAA | 23607 |
rs535053659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47536718 | TCAGGAAAAAGTTGA[C/T]TACTGTAAGTTGCTA | 23607 |
rs535059637 | in-del | -/T | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520091 | GACCTGTGGAAATGA[-/T]TTTTTTTTTTTTGTT | 23607 |
rs535081554 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47618387 | GTATATATAATAACT[G/T]CCTATATTTTCACTG | 23607 |
rs535086485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47567081 | TGTTTTTCTGATTTC[C/T]CAGTTTTTTTTTTTT | 23607 |
rs535092485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47616380 | ATTACAGGCATGAGC[C/T]ACTGCACCTGGCCTT | 23607 |
rs535093752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47584928 | AAAATCATGTCACCA[A/G]TTAGTCAGCAGTTTT | 23607 |
rs535153702 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47574376 | TAATAATTTGGTTAT[C/G]AATGAGGAGGCTGTG | 23607 |
rs535174369 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47488494 | TACATTATTTCATAA[A/T]GTATTCAGTATAAAA | 23607 |
rs535203328 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47526193 | GATAGCCAAAGAGTA[C/G]TCTGGTAGAGGCACT | 23607 |
rs535225275 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47609648 | AGGCTGCAGTGAGCC[A/G]TGAACATGCCAGTGC | 23607 |
rs535239455 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47502222 | CATAGCAGCTTGTGT[C/T]TTCAAAGCGAGCAAG | 23607 |
rs535242974 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47607489 | ATCTTTTGGATAAAA[A/G]CCATTTTAATTGGGG | 23607 |
rs535245157 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47496004 | TAATTTCCTATATGA[A/T]GTTACTGTTTTTATT | 23607 |
rs535255780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47543872 | TCACAAGCTCCCAGG[C/T]TACACTGTTGCTGCT | 23607 |
rs535257192 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47519615 | GATTGTTTGGTAGCA[A/G]TTAGATTTTGTGTGT | 23607 |
rs535333456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47500319 | CATGTGAGCCTACGT[C/T]TTCTGAATTTCTGGT | 23607 |
rs535335612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47536125 | GCTGCAAGGACTATA[C/T]TGGTTATTTAGTGTC | 23607 |
rs535343812 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47499353 | GTATCTGTGTATACA[C/T]ACATGTATACATATA | 23607 |
rs535385500 | in-del | -/A | 0.00398564 | 0.0444627 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626983 | CTTTCAATAACTGTT[-/A]ACGTAATGCAGTTGA | 23607 |
rs535418602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47541738 | CCGCATTGTAATTTT[A/G]TGGCCCAGGAAATTG | 23607 |
rs535420550 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47549712 | TTAGAAAAAACAATT[A/C]TAAAATTCATATGGA | 23607 |
rs535431429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47576874 | CGGTATTGACTATAA[A/G]TATTTTAAAATTTAA | 23607 |
rs535470840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47540353 | TTTGAAATGTGAAAA[A/G]TCTCAAAGTGCCCCC | 23607 |
rs535570318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47577565 | GAAAATGATGTCACC[A/G]TTTTAAAGAATGAAG | 23607 |
rs535634108 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47519243 | ACATTGATAAGTTGG[G/T]TGGTCTAGAATAACA | 23607 |
rs535670213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47546919 | AATTTTGTATCCAGC[A/G]AAACTTAGCTTCATA | 23607 |
rs535691174 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47584267 | ATCATGGCTTTGGTG[G/T]TGTATCTAAAAAGTC | 23607 |
rs535692013 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47518543 | GTTTATCCTCTTTTT[A/G]CCTGTTGGTGGATAT | 23607 |
rs535699954 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47621998 | GTCTGAGCTCACGCT[C/G]TTCTTGGGCGGGTCT | 23607 |
rs535728396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47505359 | GGCAAGGTCACAGAT[C/T]AACAGGATCCCAAGA | 23607 |
rs535760693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47512290 | GAGGTTGCAGTGAGC[C/T]GAGATCGCACCACTG | 23607 |
rs535782787 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47590892 | GAAAACATTGAGGCA[A/G]GGAATTGAAGAAGAC | 23607 |
rs535795419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47545393 | TGCCTAGCCCCGCCC[A/G]CACCTAATGGTCCTT | 23607 |
rs535797413 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47552981 | TGTCATTTCCTTTTG[C/G]GGGGGAGCATTTTTT | 23607 |
rs535806930 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47515243 | AAAGCATGGGTTAAA[A/G]TAGGGGGTACAGTAT | 23607 |
rs535811916 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47563944 | TTTAATTTAGTTTCA[A/G]TTGTTTTAATAGTTT | 23607 |
rs535821041 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47489354 | TGTATTATTATTTTT[G/T]TAGTAGAGATGGGGT | 23607 |
rs535825924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47592320 | AATGAAGTTGGAGCC[C/T]TACCCCACACTGTAA | 23607 |
rs535832767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47544193 | CTTACTGCTTCTTTC[C/T]ATAGTCGTAAAAGTA | 23607 |
rs535884740 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47490014 | AGGGTCTTGCTCTGT[C/T]GCCTAGGCTGGAGTA | 23607 |
rs535892830 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47531847 | GGAGGTCGAGGCAGG[C/T]AGATCACCTGAGGTC | 23607 |
rs535955646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47537028 | TGGAAACTCACGCTA[C/T]AGCAGAAGTGATTTT | 23607 |
rs535963142 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47585569 | CAAACAGACCTCGAT[A/G]TCCTACAGAGTTGAG | 23607 |
rs535979082 | in-del | -/AGC | 0.00597247 | 0.0543191 | intron-variant | CD2AP | GRCh38.p7 | 6:47578059 | TGTTTTAGTGGCAAT[-/AGC]AGCTAAAATCATTTA | 23607 |
rs535982234 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47588721 | TTTCCATTCTGCCAT[C/G]CTCAGTGTACACTTT | 23607 |
rs535989953 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47501779 | TGTTATTGCTTTTTA[A/G]AAATTGAACCTTGTA | 23607 |
rs536036078 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47514479 | TTGATTCAGTATCAA[A/T]GTCTTGGCTAGTTCA | 23607 |
rs536048829 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47563235 | TCACATCTCTAGGGG[A/G]AAGACAAATGTGAAG | 23607 |
rs536055860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47570828 | AGTTCATATACTTTA[C/T]CGCTATACCATGCTG | 23607 |
rs536070478 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47564122 | GTCAGAACTGATGTT[C/T]AAGGGTGTGTAAAAA | 23607 |
rs536081245 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521942 | ATTGCTTGAACCTGG[G/T]AGGCGGAGGTTGCAG | 23607 |
rs536104192 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47617409 | CCTCTAAATCAAATT[C/T]GTATTTTCCCAGCTT | 23607 |
rs536192392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47556178 | CGTCATCTACATTAG[A/G]TATTTCTCCTAATGC | 23607 |
rs536196395 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47512348 | CTCTGTCTCAAAAAA[A/G]ACAAACATAAAAAGG | 23607 |
rs536236000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47603416 | TTTAGTTATAACTAC[A/G]TTATGAGATGTCAAC | 23607 |
rs536243244 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47606705 | GGTACATAATAGATT[A/T]GTATATTTATGGGTT | 23607 |
rs536243596 | in-del | -/GAGGTT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47579262 | ATCACTTGAGCCCAG[-/GAGGTT]GAGGCTGCAGTGAGT | 23607 |
rs536248282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47568468 | ATGAGTAGGCTGGGC[A/G]CGGTGGCTTATGCCT | 23607 |
rs536276372 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47574354 | AGATTTCTTTTTTTC[A/G]GATCACTAATAATTT | 23607 |
rs536294722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47602862 | CCTTGATCATGCCAT[C/T]GCTCTCCAGCCTGGG | 23607 |
rs536302388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47510859 | GTGGGCAGATTACGA[A/G]GTCAAGAGATCGAGA | 23607 |
rs536364274 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47500989 | CCTGACCTTGTGATC[C/T]GCCTGCCTCCGCCTC | 23607 |
rs536390358 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47571071 | CTCAAACTGTGAAAA[C/T]TGTACTTTAGAATAA | 23607 |
rs536407205 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47582422 | TAAGCATGAAAATAA[A/T]TAATTACATATTATT | 23607 |
rs536407854 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47591792 | TTAGACATTTTTGTT[-/A]AAAAAAATTATATAC | 23607 |
rs536413362 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47486904 | TTAGAGTGTTTTTGG[C/G]GGACATTTAAAGTTG | 23607 |
rs536418416 | snp | A/G | 8.29084e-05 | 0.00643796 | intron-variant | CD2AP | GRCh38.p7 | 6:47609331 | TTCTTTTCTCCTGTG[A/G]GTACTACTTAACCCA | 23607 |
rs536468808 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47478895 | TGAGGAGCAGTTTCC[G/T]GTTTGGAGTTAGACT | 23607 |
rs536489207 | in-del | -/A | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47627017 | GTAACCTAACATTCC[-/A]AAAAAAAAAATTGAG | 23607 |
rs536534448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47559595 | TCAGATAATATTTTA[A/G]AATTTAATAGATGAT | 23607 |
rs536568720 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47561429 | AAGCTCATTTTGAAC[C/T]TTCCCTACCCTAGTC | 23607 |
rs536572323 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47583218 | TGTTAACATTCTGTA[C/G/T]CAGAGTGGCATATTT | 23607 |
rs536575203 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47575181 | GCATTAGGATTGTGG[G/T]GTCAAATTGATTCTT | 23607 |
rs536598589 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47567000 | AATGTCACTCCCATT[G/T]TAAGGGTCAAGAAGT | 23607 |
rs536610703 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47615726 | ACACAGATGCAAATC[G/T]TATCAATGATTAAGT | 23607 |
rs536614151 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47612056 | TTTAAAAATAGAGAA[A/C]GAAATTCAAAGTCTA | 23607 |
rs536671437 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47541174 | TGTTGCCCAGGCTGG[A/G]GTGCAGTGGCACGAT | 23607 |
rs536688334 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47516241 | ACTGTGCTGCTTTTC[A/C]TGTGGCGGCACAACC | 23607 |
rs536688446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47524518 | AAACTATTAGGAAAA[A/G]TGTGACCATTATAAA | 23607 |
rs536697611 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47619555 | TATCTTTTTCGAATA[A/G]TGACTTCTTTTCCTC | 23607 |
rs536703874 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47502798 | CACCTGGCCTGAACT[C/T]CTGAGTTTAAGTGAT | 23607 |
rs536737460 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47554284 | TTAAATAATATACAA[A/T]TCAAGCCTTAGTAGT | 23607 |
rs536755449 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47607874 | TCCAAAGACTTACTA[A/C]CTTTTCTTTTCTTTG | 23607 |
rs536760287 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47513034 | TGTCAGGACAATGAG[A/G]AAGTGTGTTAGTTTA | 23607 |
rs536768090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47510224 | GGAATGGTTTTGTAT[A/G]TATATGTGTCTGTGT | 23607 |
rs536789853 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47561462 | GGAATCAGCTACCTA[A/T]CAAGGCAAACTTTTT | 23607 |
rs536810305 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CD2AP | GRCh38.p7 | 6:47481414 | GCTGTGGTGCGATCT[C/T]GGCTCACCGCAACCT | 23607 |
rs536866880 | snp | G/T | | | downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47627321 | TTTTTCATCTGAAAC[G/T]GAGACAGTAATTTCT | 23607 |
rs536873704 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47550198 | ATGCACTAAAAACAG[A/G]TAAATAGCTATGACC | 23607 |
rs536876268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47537667 | CTTCATGATAGTGAT[A/G]ATGAAGATTTTCTAA | 23607 |
rs536879584 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47541661 | TTACTTTTTGTCTTG[A/T]TAAACAATTTCGTAG | 23607 |
rs536904465 | in-del | -/TTTG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47538937 | TTCACACAATTTGGT[-/TTTG]TTTTTTTAAAAATAC | 23607 |
rs536922417 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47579192 | ATCATTTGAGCCCAG[A/C]AGTTTATGATTGCAT | 23607 |
rs536922900 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47512996 | CACTAGTTAGCTTAT[A/G]GGTAATTAGTAGAGA | 23607 |
rs536949897 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47486052 | TAGTTACAGTTAACA[A/C]CAATATTAAGAAAAA | 23607 |
rs536950650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47523803 | AAATGCCCTATAACA[A/G]TGTGACATAACACTG | 23607 |
rs536984084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47578491 | TTACTGGGATTACAA[A/G]GCATGAACCACTGTG | 23607 |
rs536984429 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47586230 | GAAAATATAAGAAAG[A/T]CCCAAATTGAACCTT | 23607 |
rs537013410 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47500339 | GAATTTCTGGTCTTT[G/T]TGAGGTCTACAGAGC | 23607 |
rs537016064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47528573 | CTGTTTTTACCAGTT[A/G]TAAATAGTAGTTTAT | 23607 |
rs537076633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47535341 | AATCCCTGTAGTACA[A/G]AATATTCTACAATAA | 23607 |
rs537081878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47519468 | GATGTGTAGACCTCT[A/G]TTTGACTTCTTTTGA | 23607 |
rs537100895 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47513792 | ACTCCTAGGGTGTGC[A/T]CATGTTCAACTATAC | 23607 |
rs537111345 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47513873 | CTGATACCATCAGAC[-/T]TTAAAAAAAATTTTT | 23607 |
rs537120294 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47557272 | TTCTCCCATTCTGTA[C/G]GTTGCCTGTTCACTC | 23607 |
rs537168934 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47616183 | TGTAACCACCACCTT[C/T]CAGGTTCAGGCAGTT | 23607 |
rs537181721 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47491718 | AAAATCTTTTATAAT[A/G]TTGCCACCAATATTT | 23607 |
rs537222902 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47499330 | GTGTGTGTGTGTTGA[A/G]TATATGTGTATCTGT | 23607 |
rs537233779 | in-del | -/TATC | 0.00676609 | 0.0577691 | intron-variant | CD2AP | GRCh38.p7 | 6:47525772 | GTACTACCTACTCTT[-/TATC]TATAAGCAAAACCAA | 23607 |
rs537276567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47482285 | ATTTGAGTAGTTTAA[A/G]TTTTGTAAAATCACA | 23607 |
rs537285568 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47558053 | TCACATCCCTTGTAA[A/G]TTGGATTCCTAGGTA | 23607 |
rs537290578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47608504 | CACTACAACTGAGAC[A/G]TAGATTTAAGAAGGT | 23607 |
rs537310528 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47610031 | GTGATCTCTAAAACT[C/T]TTCCCTTAACTCTGA | 23607 |
rs537333259 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47543762 | CTATTGCCAGACACA[C/T]TGGGTGTTAGGGTTT | 23607 |
rs537335010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47622127 | TCAGGGAAGTAGGGG[A/G]AAGCTGGCAGTCACA | 23607 |
rs537388131 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47547806 | GTAAATTTAAGAAAA[C/T]TGAAATTATATCAAG | 23607 |
rs537410390 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47539318 | TAATTTTGTACTGGG[G/T]TTGTCAAGCAGAGTA | 23607 |
rs537412633 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47627011 | TGATGTTGTAACCTA[A/G]CATTCCAAAAAAAAA | 23607 |
rs537416008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47531617 | AACAGCACAACTCTC[A/G]AATTTTGGAAATGAT | 23607 |
rs537417435 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47484109 | GTCTTTGGCAATACT[C/G]CCTCATACTCCTCCC | 23607 |
rs537436685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47590794 | ATTTGAAGATACAAT[A/G]TTTTTCAATTTTCTA | 23607 |
rs537438086 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47564646 | TTTTTTTTTCTTTCC[C/G]CAACTCTAAATTTTA | 23607 |
rs537449478 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47587793 | TAACTTTTATCTTAT[C/G]TCCTCCTCACTTCCT | 23607 |
rs537482196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47544385 | GTAAATGGTGGGATA[A/G]GATGTATAAAGAGAT | 23607 |
rs537505521 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47508191 | TCTACTTATGAAAGT[C/T]CTAGGTGGTACCTTT | 23607 |
rs537515774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47573650 | CCTGCCACCATGCCC[A/G]GCTAATTTTTTTATA | 23607 |
rs537525086 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47613509 | TTTAAAAATAATCCT[-/T]TTTTTTTTTTTCCTG | 23607 |
rs537529054 | in-del | -/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626697 | TAACAGAAGATACTC[-/T]TTTTTTATGCTCCTT | 23607 |
rs537568496 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47557685 | GTTCCATTGGTCTAT[A/G]TATCTTTTTTGGTAC | 23607 |
rs537576731 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47580566 | AGGAATCTTAACCTA[A/G]GGGAGGCAGAGCAGA | 23607 |
rs537594776 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47550453 | ATGAAGACATGTTCA[A/C]CATCACCAATTATCA | 23607 |
rs537606369 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47541002 | GTTTTCCTATAGCAC[C/G]CAAAAAACTATTTAA | 23607 |
rs537619924 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47616627 | TTTTTCCATTATTCA[C/G]AATCAAAGAATAGCC | 23607 |
rs537628253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47596203 | ATGATGTTTTAAAGC[A/G]TATATATAATTCATT | 23607 |
rs537631403 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47586356 | CATAGCAAATAGAAC[A/C]ATTAAAAATGTATAG | 23607 |
rs537638988 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47507348 | GCTCCTCTCATGAAT[C/T]ACAGATGTTATTAAT | 23607 |
rs537653268 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47613029 | CACCTCACAAAGCTA[C/T]TTTCTTTGCTGATCC | 23607 |
rs537657608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47557783 | AGCTTTGTTCTTTTT[A/G]CTTAGGATTGTCTTG | 23607 |
rs537657691 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47549930 | AGCTAACTGATCTTC[A/G]ACAAAGCAAACAAAA | 23607 |
rs537708733 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47594622 | CAAATAGCTTTATTT[C/T]GTTATTGATTTCAAT | 23607 |
rs537797209 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47606088 | AATTTATAGTTTGTC[C/G]AAAAACTGAAACATT | 23607 |
rs537802365 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47548349 | AATCCAAATAAGCTC[A/C]GTTAGAAACAAAGCA | 23607 |
rs537839318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47583421 | CTTTATTCTACCTAT[C/T]CATCTGTCCTTCCCT | 23607 |
rs537863504 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47568467 | GATGAGTAGGCTGGG[C/T]GCGGTGGCTTATGCC | 23607 |
rs537909424 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47618504 | TCCTAACACAATGCT[A/G]TATACATATTAGATA | 23607 |
rs537910367 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47592265 | GCAAATTTTTAGCTG[A/T]ACTAACATTCTAGTA | 23607 |
rs537939049 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47480390 | TTTATCTAATTTGTC[A/G]CAAAATGAAAAAATC | 23607 |
rs537940236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47549090 | TGCAAAACCACAGCC[A/G]ACATAATACTGAATG | 23607 |
rs537948300 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47486940 | TTAAATGTATATACT[A/G]TTCTCTAGGGATTTT | 23607 |
rs537950600 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47616678 | TTCTTGATGTACTGC[A/T]GTTACTTTCTCTTTT | 23607 |
rs537975116 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47599575 | ACAGTTGAAATTTGT[C/T]TAAAATTTAGCAGCC | 23607 |
rs538007504 | in-del | -/TA | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47611985 | GAGTTGAGGAGAGAC[-/TA]TTGGCTAGAGTTTTT | 23607 |
rs538055346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47553213 | GATGACTAACTTAGT[A/G]AAAGGTTGCCTACCT | 23607 |
rs538063810 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47536968 | AAATCTCTTGGCACA[C/T]GTGAGGCAATACATA | 23607 |
rs538083492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47495352 | CGTAAGCAAAGGAAC[A/G]CTAAAAATTGCTGGC | 23607 |
rs538090957 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47525433 | CTGCCTGTTTCATTT[C/G]AGAAATGAAATGAAG | 23607 |
rs538136711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47546807 | AACCTATAAAGGACA[A/G]TCTATCAAATTAACA | 23607 |
rs538139928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47563215 | GTAGTCCAGAGGTGC[A/G]AGTATCACATCTCTA | 23607 |
rs538161316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47597139 | CCTCATGCATGCTTA[A/G]AACACTTGGGGGAAT | 23607 |
rs538173206 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47567533 | ATTTAAAAAAGTGAT[C/T]GTAATTTAGCAGGAG | 23607 |
rs538202815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47569854 | ATTAGTATTCACCTT[A/G]TACTCCTCCTGGTGA | 23607 |
rs538211284 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47551383 | TTTTTATGTTTATAC[A/C]AACTTAGATTGTGTT | 23607 |
rs538224047 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47606767 | CATAATAATTATATC[A/T]GGGTAAATGCGGTAT | 23607 |
rs538252312 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47614821 | CTATTTTCATTCTTT[C/T]TTTGCTCAGGGACAG | 23607 |
rs538265362 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47558763 | ATTGATGTTCATCAG[A/G/T]GATATTGGCCTGAAA | 23607 |
rs538281276 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47497580 | TTACTCCTGACTACA[A/T]TTTTTTGGTATTTTT | 23607 |
rs538296330 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47585381 | GTGGAATGACAGGGA[C/T]CGAATTTACACTCCT | 23607 |
rs538329638 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47540737 | ACCTTAAGTCCAATT[G/T]TAAGAGATATTAAAA | 23607 |
rs538347527 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47544777 | TTAGAAAAATTAATT[A/G]TAAGAATATTAGTCT | 23607 |
rs538358391 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47591746 | AAAAGGACATATTTT[C/G]GTTATTTTGTTGTAT | 23607 |
rs538366832 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47505187 | GCGGCCTTCCGCAGT[A/G]TTTGTGTCCCTGATT | 23607 |
rs538391562 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47478887 | GGATCCTTTGAGGAG[C/T]AGTTTCCTGTTTGGA | 23607 |
rs538409950 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47612750 | TTATGTTAAGCCAGG[C/G]ACAGAAAGAGAAACT | 23607 |
rs538411221 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47517718 | ATCTTTTGATGGATA[G/T]AGACAATCTGGTATA | 23607 |
rs538429908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521176 | TTGTAATGCACATCC[A/G]TAACAGTTGCTTATC | 23607 |
rs538448817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47577434 | CTTCCACCTCATTCT[A/G]TTTTTTCTCCTGTCT | 23607 |
rs538462423 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47572800 | GAATGTTAAGAAGCT[C/T]ATGTGGGCTTATAAA | 23607 |
rs538498722 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47623047 | GCTGACAATGAAAGC[A/T]ATCGTCTCAATCCAA | 23607 |
rs538526278 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47558343 | TGATTGCCCTGGCCA[A/G]AACTTCCAATACCAT | 23607 |
rs538593257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47565559 | TTAAACCTAAGATGC[C/T]CAAAATTGATCCTCT | 23607 |
rs538649850 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47514854 | GTCAGGAGTTGGTGA[C/T]CAGCCTGGCCAACAC | 23607 |
rs538653057 | in-del | -/AC | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47546949 | AAATGAAGGAAACAT[-/AC]AGTCTTTTTCAGACA | 23607 |
rs538662239 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47581873 | TGGTAATTCCGGTAC[A/G]TTGTTCTTTCTATTA | 23607 |
rs538685410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47507523 | CAACCTCTGCCTCCC[A/G]GGTTCAAGCGATTCT | 23607 |
rs538688158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47595546 | AAATCATGTGTGGTT[A/G]TATTTGAGATAGACT | 23607 |
rs538690614 | snp | A/T | 0 | 0 | intron-variant | CD2AP | GRCh38.p7 | 6:47618093 | GAAGGTCAAGGTGGG[A/T]GGATCACCTGAGGTC | 23607 |
rs538738543 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47584668 | CTTTCAAAATGGAAG[G/T]TTTTTTATATTCTTT | 23607 |
rs538739578 | snp | C/G | 0.000518762 | 0.0160969 | utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47478226 | CGGACGTCGGCTTCT[C/G]CCCGCGGGAGCCCCC | 23607 |
rs538741913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47568342 | AGGGATGTGAGAGCA[C/T]CCAAATGAAGATATT | 23607 |
rs538756229 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47611383 | TTTCTATGGAAGAGG[G/T]GGGGAATAGGATTAA | 23607 |
rs538765810 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47544815 | GAACTGTTGTCACTT[C/T]TTAAAAAAAATGGTA | 23607 |
rs538779478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47623804 | ACTAAACAGGTCTCT[A/G]TTCTTTTTACTGTTG | 23607 |
rs538791925 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47616597 | ACTTCACTACTTTGC[A/C]TGAAAATACTTGACT | 23607 |
rs538839979 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47571649 | CCAGTCTGTGAATGC[A/G]TACAGTGAAACCCCA | 23607 |
rs538878358 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47477650 | GCGCGACCCCCGGCC[A/G]TGACGTCACCGCACC | 23607 |
rs538892574 | in-del | -/TA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47598539 | ATAAAGAAATTGTGG[-/TA]TATATATATATACCA | 23607 |
rs538892946 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47485838 | TGCCTACAGTATTGA[A/G]TACAATAGCATGCTG | 23607 |
rs538932995 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47574565 | AAGCTAAAATTATAT[A/T]TAAATTTAGTTATAT | 23607 |
rs538936387 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521691 | AAACGTAGTTGATAC[C/G]CTTTAAGTTATGACT | 23607 |
rs538943342 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47608684 | AAATAGTTAAGGGGT[A/G]TCAGGCTATGGACTC | 23607 |
rs538944816 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624921 | TAGAATATTTTATGT[C/T]GCTTGCACTATAGGA | 23607 |
rs538951473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47617358 | TTTGAATTCATCTAT[A/G]CTCATGAATCTAATG | 23607 |
rs538969214 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47573614 | CTGCCTTAGCCTCCC[A/G]AGTAGCTGGGACTAC | 23607 |
rs538978699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47581432 | AAAAATTTCTATTTC[C/T]TAAAAGATTTGCTGT | 23607 |
rs538979156 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47618821 | GTGAGCTGTTACTTG[A/G]CCTCTCACTGACTTG | 23607 |
rs538997443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47523683 | AATTTCACATAGACT[A/G]TATTCAGTGAGTTGG | 23607 |
rs539038811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47526818 | ATTTTTTCAATGTAG[A/G]TAGCTTATGAGGCAG | 23607 |
rs539042888 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47613189 | GAATCATCTTCCAAA[A/G]TATTGACATTTTGAC | 23607 |
rs539067013 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625695 | ATTTTTCCTTTAAAT[C/T]TTAATCTTATAATAT | 23607 |
rs539068335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47530457 | ATTTTTAATGTACCA[C/T]ATATATTTTGTGTCT | 23607 |
rs539086760 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47621517 | TTCGTTTTTGGTTAC[A/G]ATCTTTTCTGGTTTT | 23607 |
rs539123850 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47553764 | TTTCATAGAAATTGA[A/G]TAATCTTATTGGTAA | 23607 |
rs539133175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47516169 | AATCTCAGTGGTGGC[A/G]TAGCACAAGGAAAGA | 23607 |
rs539169929 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47567854 | CACAGAGAAGCCATA[C/G]AGCAAAATCATGAGA | 23607 |
rs539189118 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47570915 | TAGCCAAAAATAGCC[C/T]ATCCATTAGTACTGG | 23607 |
rs539190361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47484994 | CCACACTATAGTAGT[A/G]CAACGCGTTACTCAC | 23607 |
rs539194684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47536969 | AATCTCTTGGCACAC[A/G]TGAGGCAATACATAG | 23607 |
rs539200026 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47526560 | GTCCCAGAGAAAATT[C/G]AAGGTTCCTAAAATG | 23607 |
rs539201209 | in-del | -/C | 0.00279162 | 0.0372561 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47627058 | TCAAAATAGTATATA[-/C]TTCACTAACTTGTTT | 23607 |
rs539242254 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47545337 | CACCCCAAATGCTCA[C/G]TCACAGCAAGATCCA | 23607 |
rs539247086 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47591690 | TGGGTTAACTTATTA[C/T]GTACAGTGTTGGTAA | 23607 |
rs539251157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47516168 | AAATCTCAGTGGTGG[C/T]GTAGCACAAGGAAAG | 23607 |
rs539264832 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47536312 | TCATTGTATTGTTAC[A/G]TAGTAGCAGGATACA | 23607 |
rs539277380 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47480769 | TGACCTTTGTTAGAA[A/G]TAGGATATTTTCTTT | 23607 |
rs539277635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47548145 | GGCACCTCAAGAAAC[A/G]AGAAAAAGAAGAACA | 23607 |
rs539304333 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47490076 | GACCTCCTGGGGTCA[A/G]GTAATCCTTCCACCT | 23607 |
rs539322704 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47493451 | TCTTATCCTTGTTCC[G/T]CAATAGGTAGGGTGA | 23607 |
rs539336655 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47529846 | GACTCAGAGAGCTTT[A/G]TATCAGCCGTCTGCT | 23607 |
rs539341114 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47600346 | CTTCATTGTTCACAT[C/T]TCATGTTTACATTTA | 23607 |
rs539354407 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47487745 | TGTTATTCTCTTAGT[C/G]TGTAAATGACCTTAC | 23607 |
rs539357708 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47496890 | TAAGGGTTTATACTT[A/T]TATTTCTTTTTCTAG | 23607 |
rs539380376 | in-del | -/AT | 0.00835141 | 0.0640778 | intron-variant | CD2AP | GRCh38.p7 | 6:47552375 | TAGCTTAGCTCCCAC[-/AT]ATGAGTGAGAACATA | 23607 |
rs539406075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47534565 | TACAAATTAGCCGGG[C/T]GTGGAGGAACTTGCC | 23607 |
rs539426286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47570144 | TTCATCAGATTTCTT[C/T]TTTTTTTTTAAGCTT | 23607 |
rs539470459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47543083 | TTGAACTCGGGAGGT[A/G]GAGGTTGCAGCGAGC | 23607 |
rs539471431 | snp | A/G | 0.000631838 | 0.0177629 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47533733 | AATTCAGCCACATCC[A/G]CAAACCAAAAACATT | 23607 |
rs539508673 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47564009 | AAGATAGAAAAATCA[C/T]TGAGGTAGGAATCAG | 23607 |
rs539519494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47579809 | TTTTATTTAATGTTG[C/T]TGAAAAGCTCTAGTT | 23607 |
rs539541276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47535192 | GTAGGAGTTATTACT[A/G]TCCTGCTGTTCAAGG | 23607 |
rs539600247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47540649 | GAAGAAATAAAGCTC[C/T]TGGGTAAAATATAAC | 23607 |
rs539629976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47505436 | TCTACCTCTTTCTAC[A/G]CAGACACGGCAACCA | 23607 |
rs539631601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47607788 | TTGAAAGTATATAGC[A/G]TCCTATTAATAATAA | 23607 |
rs539690011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47577718 | TATAACCCTGTAGAA[C/T]AATTTTTGAAATTCT | 23607 |
rs539691763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47615558 | GAGTGGGAGGGGCCA[C/T]GCAGTTTTAAACAAC | 23607 |
rs539727117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47549792 | TCTGGAGACCTCACA[C/T]TACCTGATTTCAAAT | 23607 |
rs539739879 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47532987 | CAGGGGCTATCAAAC[C/T]ACCAGCCCACAGGAC | 23607 |
rs539779568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47543706 | TTAGGGTGTTACCCT[C/T]AGGACCTCATTTAAC | 23607 |
rs539798344 | in-del | -/A | 0.0926562 | 0.194275 | intron-variant | CD2AP | GRCh38.p7 | 6:47579335 | GCAACACTTTATCTT[-/A]AAAAAAAAAAAAAGG | 23607 |
rs539799191 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47507728 | GAGATTACAGGTGTG[A/G]GCCACCGTGCCTGGC | 23607 |
rs539804048 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47511210 | CCAGTGATAGGTTAT[A/G]TTGATACCATGTATT | 23607 |
rs539858708 | in-del | -/A | 0.00835141 | 0.0640778 | intron-variant | CD2AP | GRCh38.p7 | 6:47533455 | TTTTATTCTTCAGAT[-/A]ATGTTTGAGCAGAGC | 23607 |
rs539859568 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47501489 | GGCTGAGAGAATCTT[C/T]GCCTGTAAAGTACAG | 23607 |
rs539926329 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47499327 | TGTGTGTGTGTGTGT[G/T]GAATATATGTGTATC | 23607 |
rs539969631 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47530982 | ATTTATGGGTTTTGG[C/T]TGGGCAAAACTAGTA | 23607 |
rs539971954 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47532028 | CAGTGACCAGAGATC[A/G]CGCTCAGTGCACTCC | 23607 |
rs540003063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47497713 | GCTGCAACTGCACCC[A/G]GACAATTATATTTTG | 23607 |
rs540027782 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47588796 | GGCAATCAGGGCGAC[A/T]TGATTTCTTGTCCAT | 23607 |
rs540044770 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47556660 | AGCTGAACTCATTCT[C/T]TTTTATGGCTGCATA | 23607 |
rs540050484 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47591649 | ATTAATGCAGTAGGA[A/C]ATTGACCCTCATCTG | 23607 |
rs540072429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47606970 | TACCGCCACCACACT[A/G]ACACCCTTCCCAGCC | 23607 |
rs540095986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47493734 | TTGGATGTTCTGTCC[C/T]GGGATTTTTTTGTTT | 23607 |
rs540104705 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47570360 | ACTGATAGCAACATA[A/C/T]ATAAAATGCAGATGT | 23607 |
rs540109292 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47499879 | GACTACAGGCATATG[A/C]CACCACGCCCGGCTA | 23607 |
rs540113238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47581159 | ATTAATCAAATTTAA[A/G]CTGTTTTAGAAAACT | 23607 |
rs540119146 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47536402 | GTTAATAGTGTAAAC[A/G]CTGCAGTGTATATGT | 23607 |
rs540119389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47545497 | TCCTCCCCATACTAC[A/G]TAGCTGATGCTCTCT | 23607 |
rs540170861 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47549257 | TGGTAAAGAGGAAGT[C/T]ACACTGTCACTGTTT | 23607 |
rs540176698 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47526403 | TAACATCTCAGTTGG[C/T]AGTATGTATTTGGAA | 23607 |
rs540180090 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47545008 | AGTGAAATAGAAGGA[A/C]TTTTGCCTTAGAAGG | 23607 |
rs540180511 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47557219 | CTTTGTAGATTCTGG[A/G]TATTAGCTCTTTGTC | 23607 |
rs540183086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47529936 | GGCAAATTTAGTGTT[A/G]TCTTCATTCCTCAGA | 23607 |
rs540202475 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625169 | CACTTAGTTCTTCAT[G/T]TTTCTCCTTCTGACT | 23607 |
rs540207370 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47602093 | GATATAAATCCCTGA[C/G]TTTGTTCACAGATAT | 23607 |
rs540247625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47502959 | ATGAATACGAGGAAG[C/T]GGGGATCATGGAGAC | 23607 |
rs540263563 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47572511 | GGGTAGATCACTATA[A/C]TTGTTAGCATTATAT | 23607 |
rs540272026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47487253 | TAAATTTTCAGAATG[C/T]GTGTCAAATGGAAAT | 23607 |
rs540299946 | in-del | -/T | 0.422158 | 0.181278 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626447 | GGGGTAAATCATGAA[-/T]TTTTTTTTCTACGTG | 23607 |
rs540309349 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47618256 | ACCCAGGAGGCAGAG[G/T]TTGCTGTGAGCCGAT | 23607 |
rs540335723 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47477307 | AAGACCAAATGCTGC[C/T]GATCCGTAAGTAACT | 23607 |
rs540356782 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47574867 | TGTTAATTTGGTGGT[A/G]AAATAGCTACAGTCT | 23607 |
rs540416338 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47561649 | ATTCATCTATTTATC[C/T]ATCTTTACTAGTACC | 23607 |
rs540428166 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47589221 | TAAGAGTTTGTATTA[A/C]GTGTTTAGTTGGAAG | 23607 |
rs540428345 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47590397 | TTTTAAAAGAAAATA[C/T]CTGAACTGAAACATA | 23607 |
rs540431825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47551603 | AGATAAGTGGTGGCT[A/G]TTTTAGTTACTGTTG | 23607 |
rs540433615 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47560236 | CTGTATTTTATCTTT[A/C]TTCTTTAGTATTTCA | 23607 |
rs540474373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47484532 | CTTTTAAAACAATTC[A/G]CTATTCTAAATTGAT | 23607 |
rs540502543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47524005 | GTTTCCTATAAAACA[A/G]ATCTTTTAAATGGAA | 23607 |
rs540503148 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47617116 | ACTACAGGCATGCAC[C/T]TTCATGCCTGGTTAA | 23607 |
rs540504496 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47610429 | GCCAAATAAAAAGTA[A/T]AAAAGAACAAAAAAT | 23607 |
rs540545768 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CD2AP | GRCh38.p7 | 6:47569416 | CTTTTGATATCTTCT[A/G]TAGAAAAGGAGTAAT | 23607 |
rs540551440 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47479246 | ATCACTTTTTGCAGT[C/T]GAGAGTTGGTACTGC | 23607 |
rs540556363 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47595719 | TTAAAATAAGTAAAA[C/T]AGTGCACATGTATAC | 23607 |
rs540609649 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47592589 | ATAACAAGCATCTTT[C/G]AACCACGTCTGAGTT | 23607 |
rs540629842 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47568883 | CTGAGGAAGATTAAC[G/T]GAAAAGAAGACCAAG | 23607 |
rs540670165 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47490374 | TTGTTTTTTGGTGAG[C/T]TCTATAAAACTTTAT | 23607 |
rs540674058 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47600098 | TTGTTAATATTTTGT[A/G]TAGTGCTTTTTGCAT | 23607 |
rs540674399 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47552624 | GTCTATTTTTGTGTA[-/T]TTTTTTTACCACTGT | 23607 |
rs540679156 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47549528 | TCAAAAGACCTCAAC[A/G]AGAAAAACTACAAAA | 23607 |
rs540692891 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47596232 | TTGTGGAATGGCTTC[A/G]GTAACTGTGATAACC | 23607 |
rs540714129 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47505523 | ATTGTCATCCTGGCC[C/T]GTTCTCAATGAGCCG | 23607 |
rs540714838 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47538866 | CATTTAGAAATTAGA[A/G]ATTTTCTGTTTTATT | 23607 |
rs540721244 | in-del | -/GA | 0.0491012 | 0.148794 | intron-variant | CD2AP | GRCh38.p7 | 6:47486430 | TAGAAAAATAAACGA[-/GA]GAGAGAGTATAGGGT | 23607 |
rs540729928 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47593392 | CAACAAAAAGACAAA[C/T]CTGTTTAAAACTGCA | 23607 |
rs540737060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47494990 | TATAATGAGACCATG[C/T]CTCTACAAAAAAATT | 23607 |
rs540775543 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47538124 | ATTCATGTAATGAAT[A/T]TTTCATTACATGAAA | 23607 |
rs540794209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47611487 | TTCGCTTTACTCTTA[C/T]AATAGTAGATCTTTA | 23607 |
rs540818063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47571208 | TATTGCTTTGTCCAA[C/T]AGGCTGGTTATTGGA | 23607 |
rs540825657 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47543009 | TACAAAAATTAGCTG[A/G]GCGTGGTGGCGCTCA | 23607 |
rs540865317 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47515677 | GTGCTTTTGAGGCTG[G/T]TGGGGCAAGTGATAT | 23607 |
rs540869452 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47619080 | TTTGCCTGATAACTA[A/C]TTTTTTTCCATACAT | 23607 |
rs540931480 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47603885 | TTCAATATAAATAGG[G/T]GGTGCACATTGATTT | 23607 |
rs540936796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47509704 | AATAACTGGATTTAA[A/G]TGCAGTCAAGTTCCA | 23607 |
rs540939803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47556913 | ACATTGTCTTCCACA[A/G]TGGTTGAACTAATTT | 23607 |
rs540954979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47564170 | TAAGTACCAAAAACA[C/T]GTGGCTTAAATTTAA | 23607 |
rs540981207 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47493866 | AATGCATCAGTGTTG[G/T]CGATTATTTGTTACA | 23607 |
rs541002883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47498988 | TATTCGATGGGGTAT[A/G]TTCTTTTAATTTCAT | 23607 |
rs541046929 | in-del | -/ACTA | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47553202 | ATTGGCTGTTAGATG[-/ACTA]ACTTAGTAAAAGGTT | 23607 |
rs541055790 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47583630 | TCAAATAATATTTCA[A/G]TGTCTTTATATTCCA | 23607 |
rs541067022 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47616862 | AGTGCCTGCAACAGA[G/T]CACATTTTTTACCAT | 23607 |
rs541103120 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant | CD2AP | GRCh38.p7 | 6:47592219 | AGAACTTTTTTTTTT[-/C]TCCTTAAATCTACAT | 23607 |
rs541112898 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47543230 | AGTGTCTTCTAAGCT[G/T]AGAAGTGAAGATGAG | 23607 |
rs541134824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47507692 | CCTCGTGATCTGCCC[A/G]CCTTGGCCTCAGAAA | 23607 |
rs541168354 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47550037 | ACTGGATCCTCATCT[C/G]TCACCTTATACAAAA | 23607 |
rs541170080 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47484610 | TCTTTCCTAGAACCT[G/T]TCCTTTCCAGTGGCT | 23607 |
rs541172006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47542457 | ATTTAATTTCCATTG[C/T]GGTGATATTAATAGG | 23607 |
rs541174411 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47482479 | CGCCTCCCGGGTTCA[A/G]GCAAGTCTCCTGCCT | 23607 |
rs541176914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47601635 | CCTTTTTAAATTAGA[C/T]GATCATATGTTCCTA | 23607 |
rs541182120 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47515143 | TGGCAAAGGTATTAG[A/G]TAATTTATGATAAAA | 23607 |
rs541211319 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47563559 | GGGTGGGGATATGTA[A/G]TTTTCTTACAAGGAG | 23607 |
rs541244683 | snp | C/G | 1.80331e-05 | 0.00300271 | intron-variant | CD2AP | GRCh38.p7 | 6:47579540 | AAGAACATTTTGCCA[C/G]TATTCTTTTGCAAAC | 23607 |
rs541262645 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47504246 | ATTCCCTGGCCTCAT[G/T]AGATTATGAGCTCTT | 23607 |
rs541265761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47622225 | CTGTTTCCAGACAGT[A/G]GGCGAGATGGGCTTG | 23607 |
rs541333507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47482762 | CATTTAAAATAAATA[A/G]AAAACTCAAAGTGCT | 23607 |
rs541340578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47512406 | ATGGAGTGTGGATGG[C/T]GGAACTAGGCTTCTT | 23607 |
rs541400249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47620744 | TTTTGTAGTTTTCCT[C/T]GTAGAGGTCTTCTGA | 23607 |
rs541482593 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47558846 | GCATCATAAAATGAG[A/T]TACGGAGGAGTCCTT | 23607 |
rs541496275 | in-del | -/T | 0.00914312 | 0.0669923 | intron-variant | CD2AP | GRCh38.p7 | 6:47537926 | GGCTAATTTTTTCTA[-/T]TTTTAGTAGTGATGG | 23607 |
rs541525816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47609408 | GTGGCTGGGTGTGGT[A/G]GTTCGCGCCTGTAAT | 23607 |
rs541548682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47612864 | GAGGGTGGGACGGAT[A/G]TTAGTGGAATTAATT | 23607 |
rs541588426 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626234 | TTTGCTTGTGTCCTC[C/T]TCAGTCAGAATAGAA | 23607 |
rs541592911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47587386 | AAGTGATTCCCCGTT[A/G]TTTCATGGGATATTT | 23607 |
rs541594644 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47487057 | AATTCCTGTTGTGCT[G/T]TAGCAGGTTGCAGTC | 23607 |
rs541620302 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47538707 | CCCACTTCTTATTGG[G/T]GTATGCTCTTATTGT | 23607 |
rs541622027 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47504833 | GTATTGAGAGTGCAA[C/T]CGCATTATATTAAAA | 23607 |
rs541644015 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476087 | GTATGTGCTTCCAAT[A/T]GCTTATATTTTTGTC | 23607 |
rs541706239 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47528715 | TTAGTCACAAAAAGG[G/T]TCACAAGTTTAGAGG | 23607 |
rs541718173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47524188 | AATACATTTTGTTTC[A/G]GCTAAGGTATTTCAG | 23607 |
rs541720278 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47627234 | AATTTCCAAATACAA[G/T]AATAAATAGTAAACC | 23607 |
rs541748495 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47531725 | TAGTTATTTTGCACT[G/T]TATTAAAAAACTAGC | 23607 |
rs541759646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47612400 | GTAGGTTAGGTAACA[A/G]AAAGCCTGTAAACAT | 23607 |
rs541760187 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47492348 | CTCACACCTGTAATC[A/T]TTTTTTTTTTTTTTT | 23607 |
rs541776897 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47583606 | CTTGGGAGGCATATG[A/T]TGTTAGCATCAAATA | 23607 |
rs541806591 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47558514 | CAATACCTAGTTTGT[G/T]GAGTTTTTTAGCATG | 23607 |
rs541819781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47533330 | TTGTATCTCAGTGTT[C/T]CTTTGTAGTTGGGGT | 23607 |
rs541821044 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47620009 | ATTTTTTCCCACTCT[C/G]TGGGTTGTCTGTTTA | 23607 |
rs541827931 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47481058 | TTCTGTGTGAAAGAA[A/T]TTGGGAAGAGCTCTA | 23607 |
rs541838328 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47585154 | ATAAAAAAAAAAAAA[A/C]CAGCTGGGTGTAGCG | 23607 |
rs541873790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47570241 | TCTTTTAAGTCACTT[C/T]ATATGAAGATACAAG | 23607 |
rs541934033 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47604750 | CAGATTATATAATGC[A/G]TTTTTCATTGTCATT | 23607 |
rs541942539 | in-del | -/TGT | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47612029 | TTTTGGATTTTAATG[-/TGT]TATTTAATTTTTAAA | 23607 |
rs541968182 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47530878 | AGTGTCTTATTTAGG[A/T]TGACACTTGTGGACA | 23607 |
rs541978312 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47478548 | CCTCTGCTAACCCCT[A/T]GCCCAGCTAAAATCA | 23607 |
rs542001488 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | CD2AP | GRCh38.p7 | 6:47580122 | CAACTCTATGGAAGC[-/T]TTAGGCTGTCTGAGG | 23607 |
rs542045753 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47589544 | TACACATATGTACAC[A/G]TATATATACACACAC | 23607 |
rs542069113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47555096 | TGAGTTTGCAAATGG[C/T]CTGTTTAATACTTCA | 23607 |
rs542102477 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47548516 | AGGAAGAATTACATA[G/T]GCTGAACAGAACAAT | 23607 |
rs542163484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47547893 | AAAACCATGCAAATA[C/T]GTGGAAATTAAATAA | 23607 |
rs542210396 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47524339 | CACTCTCATCTGTGG[C/T]CTCAAGGAGTCTAGC | 23607 |
rs542221644 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47589659 | GATAGAGGGGAAGAG[A/G]AGAGCCCAGTAAAGT | 23607 |
rs542228349 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47510409 | TCCTTGGAGAAATGA[C/T]TGATTCTGGTGTTTG | 23607 |
rs542229554 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47619783 | GGAGTAAGGTGGTAT[C/T]GGATTGTGGTTTTGA | 23607 |
rs542230233 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47544829 | TTTTAAAAAAAATGG[G/T]ATAGAGTTTCTTTAC | 23607 |
rs542248429 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47545411 | CCTAATGGTCCTTTC[C/T]TACCCACCCTAGTAA | 23607 |
rs542263563 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47578750 | CAGCCTCTGCCTCCC[A/G]AGTTCAAGCAATTCT | 23607 |
rs542265189 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47573932 | GCTCTTCTGGATATT[G/T]CAGTACTGAATAGTT | 23607 |
rs542265233 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47581597 | TTTACTCTTCAATGT[C/G]GTAGCCACTAACCAT | 23607 |
rs542272367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47535767 | TACAGCTGAACCTCT[A/G]TATAGAATGTCTGTG | 23607 |
rs542282675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47591804 | TGTTAAAAAAATTAT[A/G]TACCTGAGATAACTC | 23607 |
rs542302552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47587654 | ACTCATCATGTCATT[A/G]GTATGAAATTCATGA | 23607 |
rs542302844 | in-del | -/GT | 0.455383 | 0.142541 | intron-variant | CD2AP | GRCh38.p7 | 6:47493351 | CAGATTTCTAGGTTG[-/GT]GTGTTTTTTTTTTTT | 23607 |
rs542319562 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47621778 | TAATCTAGGAGGGTT[G/T]TATTTTTCCAGAAAT | 23607 |
rs542328291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47581025 | TAAACATTTTTAGAA[A/G]TATATGAAAATTGAG | 23607 |
rs542332108 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47594204 | TAAAGGTGGTGGTTG[C/G]GTAACATCGTGAATG | 23607 |
rs542352347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47488863 | GCCATTGCACTCCAG[C/T]CTGTGCAACTGAGTG | 23607 |
rs542364707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47502637 | TAGCTGGGATTACTG[A/G]CGCCCACCACCATGC | 23607 |
rs542369998 | snp | A/C | 0 | 0 | intron-variant | CD2AP | GRCh38.p7 | 6:47483587 | ACCAAGAGGTAATAA[A/C]AAGACACTGAGCCCC | 23607 |
rs542395250 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47504252 | TGGCCTCATTAGATT[A/T]TGAGCTCTTCTAGGA | 23607 |
rs542407490 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47598326 | ACTAGTAGAACCACT[A/G]TGGAAAGCAGTGTGG | 23607 |
rs542456298 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47568189 | GGGAGATGATGATGT[A/G]TCGTTAAAATAGATG | 23607 |
rs542456677 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47501331 | ATACATAGACTATCT[C/G]TAGACCTTTGCCTCT | 23607 |
rs542473182 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47485242 | GGGTATTCCAGAAAA[A/G]GGCATTGTTATCGTA | 23607 |
rs542489989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47544097 | AGCTAAAGTAAAATT[A/G]TCTTCAAATAAATGA | 23607 |
rs542510914 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47591258 | GGTGGGGTAGTGATT[G/T]GGAAGAAGGATAAGG | 23607 |
rs542543758 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47598936 | TAATAAAAAAAATTT[A/T]AAAAAAAATACAGGA | 23607 |
rs542551269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47550846 | GTGCTGGAATACTAC[C/T]CAGCCATAAAAAGGA | 23607 |
rs542563675 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47536361 | TATTAATTTAAAAAA[A/C]CCCAAAACCATTGTA | 23607 |
rs542575880 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47595856 | TGAAATATTTTAAAT[C/G]TTAGATGAAAAATCA | 23607 |
rs542639701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47603111 | CCTGTTGAGTAGCAT[A/G]TACTATAAAAAGTGA | 23607 |
rs542650192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47595025 | GCTTCTTATTTTTGT[A/G]TATACGTCTTAAGAC | 23607 |
rs542656829 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47561009 | TCAGTGTGGGCTCAT[C/T]AGAGGGTTCTGTTTT | 23607 |
rs542676104 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47572894 | GGTAACTACTATTTT[G/T]ATTGTCCCTATTGTT | 23607 |
rs542676407 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47600629 | TGTATTTTAGAGAAA[C/T]TCATTGAAATTTATT | 23607 |
rs542683292 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47611454 | ATATTTTATTTCTTT[A/T]CTTGGAGTTCAGAGG | 23607 |
rs542743487 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624303 | GCTGACTTGTTACTT[A/G]AAAATTGTGAATTCT | 23607 |
rs542755418 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47492796 | GATGTTTTCAAATAA[C/T]AGTTTTTGGTTGCAT | 23607 |
rs542790697 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47598771 | GGGTGGGAGGGGAGT[A/G]AAGGATAAAAGACTG | 23607 |
rs542816637 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47573070 | TCTGATGAAAGCTGT[A/G]CCTGTTTTATCCAGA | 23607 |
rs542818873 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47615668 | TCTCACCTGGCCCCA[C/T]CTCCAACACTGGGGA | 23607 |
rs542843078 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47566730 | TTTGGTTTTCTGTTC[A/C]TGTGTTAGTTTGCTG | 23607 |
rs542848776 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47514054 | GTTCTTGTTCATATT[A/C]TAGTTAATTTCTAGT | 23607 |
rs542858011 | in-del | -/GAGA | 0.00122875 | 0.0247561 | intron-variant | CD2AP | GRCh38.p7 | 6:47486428 | ATTAGAAAAATAAAC[-/GAGA]GAGAGAGTATAGGGT | 23607 |
rs542863562 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47617787 | TCCATTACATGCTGA[A/C]TAAAGTTCCAACAAC | 23607 |
rs542870226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47608746 | TGTTCACAATTACTT[C/T]TAAGTGAAGCTCTTT | 23607 |
rs542878242 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47577420 | TTATTCTTACTTCTC[G/T]TCCACCTCATTCTAT | 23607 |
rs542890568 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47500544 | GAAACTACTTCATGT[A/C]ACGAATCTGAAGGTA | 23607 |
rs542947554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47602266 | TTTTAGCTTCTTCAT[A/G]TATATTCTCATATAT | 23607 |
rs542991247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47504818 | TGTTTACATTATACT[A/G]TATTGAGAGTGCAAT | 23607 |
rs542999478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47497385 | CTTCTCCTTCCCTGT[C/T]GCCTTCCCTTTTTCC | 23607 |
rs543009861 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47542394 | CAAAAATATGTAGCA[A/G]ATACTGCTGTAGTTT | 23607 |
rs543044145 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47606351 | AAGATAGAGGACTTA[G/T]AGCTCTACCTAAGTT | 23607 |
rs543049057 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47509002 | AACTTTCAGCATTAC[G/T]TCCTCACTAAACTTG | 23607 |
rs543090211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47512083 | GAATGGTGTGAAGCC[A/G]GGAGGCGGAGCTTGC | 23607 |
rs543128441 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47501423 | GCTGACCTGATTGTA[C/T]TTAGTGTCTGAGAAG | 23607 |
rs543130929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47546254 | AACAAGCAGAAGAAA[C/T]AACTTCAGAGCTTAA | 23607 |
rs543172205 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47578657 | TCCTTTCATTATATC[-/T]TTTTTTTTTTTTTTG | 23607 |
rs543193816 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47545660 | GGTGCTGGTATCCAC[A/G]GCTAAGAGACCCACG | 23607 |
rs543210235 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47522929 | TATGTATATAGCTAC[G/T]TTGGAAAGTCTCATT | 23607 |
rs543211800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47577873 | GTGAGCTACCACACC[C/T]GGCCCCATTGTTTTA | 23607 |
rs543224940 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47621588 | GGGTTCCTTCTTTCT[C/T]TATCTTGTGGAATAG | 23607 |
rs543255322 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625109 | CAGCCTGTTGCTGTA[C/G]TTTTCTGCTTATTTT | 23607 |
rs543295657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47610227 | GTTTAGAGATGTTTT[C/T]TATAACCACTAGTAT | 23607 |
rs543373969 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47599174 | AGTTTTGCGTTTATG[A/G]AAATGGTTTTACAGA | 23607 |
rs543388687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47570212 | TCTCCAAACAAGTAA[C/T]TGCATTTTGCAGTTC | 23607 |
rs543418393 | in-del | -/GT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47581040 | ATATATGAAAATTGA[-/GT]GTTCACATGCATTAG | 23607 |
rs543433297 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47504640 | AGTTGTGGAGCCTGC[A/G]GATGTGGAGGGCCGA | 23607 |
rs543442175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47527895 | TAGTAAAAATCAAGT[C/T]GTCGTCTTTACCTAC | 23607 |
rs543518205 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47549355 | AAGAATTCAGCAAAG[G/T]TTCCGGGTACACAAT | 23607 |
rs543518584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47505479 | ATCTCTTCCCCGCCT[C/T]TCCCGCCCTTCTATT | 23607 |
rs543526974 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47557568 | GTTTTTCCAACAACA[C/T]TTATTAAATAGGGAA | 23607 |
rs543532433 | snp | A/T | | | missense | CD2AP | GRCh38.p7 | 6:47579417 | CTGGTGGAGGGGCGA[A/T]CTTAATGGTAAAGAA | 23607 |
rs543567539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47517955 | TGATCAGCATTTTAC[A/G]TAAATAAGATGGATA | 23607 |
rs543580762 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47548857 | AAGATAATACACCAC[C/G]ATCAAGTGGGTTTCA | 23607 |
rs543602266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47569527 | GCCATTTATCCCTCT[A/G]GGCTTTACCGGGCAA | 23607 |
rs543604572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47534092 | GATTCTTAGCATAGA[C/T]ACAAGAATTTTGATA | 23607 |
rs543613981 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47537923 | CCTGGCTAATTTTTT[-/C]TATTTTTAGTAGTGA | 23607 |
rs543626706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47481771 | TAAAAATTTTTATTT[A/G]TATGTTATTTATTTA | 23607 |
rs543630958 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47585782 | AAGCAATAGGTGAAG[C/G]ACTCTTTGTAACTCA | 23607 |
rs543657860 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47538465 | TGGTCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 23607 |
rs543672442 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47525790 | CTATAAGCAAAACCA[A/G]TCAGTATAGCACATT | 23607 |
rs543700164 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47527255 | GTGCTCCTACACTCA[A/G]TGAAGAAGTATACCT | 23607 |
rs543700853 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47592542 | TGAAATTTCCTGAGT[G/T]ATAAAGGTGAGAGGA | 23607 |
rs543703258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47480901 | TGGATGTACTGTGCG[A/G]AAGTCCATTATTGGT | 23607 |
rs543769785 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47489499 | CTAGTTTTTTAAAAA[A/G]TAAAGGTCTGTTTGG | 23607 |
rs543778096 | snp | A/G | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521784 | ACTTTGGGAGGCTGA[A/G]GCGGGCAGGTCACCT | 23607 |
rs543779006 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | CD2AP | GRCh38.p7 | 6:47499237 | AAGTCGTGGCATTTG[C/G]TTTTCTCATTACCAT | 23607 |
rs543832046 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47523183 | AACAATTCAAGAGCT[A/G]GCTTTATAATAGTTC | 23607 |
rs543868387 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47529301 | GATGAAAAAAAATTG[A/G]TTCCTAGCTGGGGCC | 23607 |
rs543870113 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47558783 | TGGCCTGAAATTTTC[-/T]TTTTTTTTGTTGTGT | 23607 |
rs543883383 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47616671 | AGCTGCCTTCTTGAT[A/G]TACTGCAGTTACTTT | 23607 |
rs543933874 | in-del | -/AACTTAAAAGTC | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47548056 | AATAACCTAACTTTT[-/AACTTAAAAGTC]AACTTAAAAGTTAAA | 23607 |
rs543947033 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47543159 | GTCTCAAAAAAAAAA[A/G]AAAAAAAAAAAAAGA | 23607 |
rs543955714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47619787 | TAAGGTGGTATCGGA[C/T]TGTGGTTTTGATTTA | 23607 |
rs544052983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47494701 | GGGGACTCCCCCATA[A/G]GACAGCATTCTCCTA | 23607 |
rs544092663 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47583451 | TTCAACCCTTGTCAA[A/C]CATTAATTTTTTTAA | 23607 |
rs544093921 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47530051 | CTTGCTAACTCTCAT[G/T]TATTCTTTCTGTCTC | 23607 |
rs544101433 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47602277 | TCATATATATTCTCA[C/T]ATATAATGTAGTTTT | 23607 |
rs544115876 | snp | C/T | 0.000819504 | 0.0202257 | intron-variant | CD2AP | GRCh38.p7 | 6:47486427 | CATTAGAAAAATAAA[C/T]GAGAGAGAGAGTATA | 23607 |
rs544134004 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47611807 | CAAACAAAAAACCTC[A/G]ATATTTGAATACCAA | 23607 |
rs544138295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47574931 | CCTATCTCTTTAACT[C/T]TGAAGAAATTATAGT | 23607 |
rs544143289 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47578964 | ACCCGGCCTCATTTT[A/T]TCTTTCTCTTTTTTC | 23607 |
rs544171712 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47537916 | CACTGCACCTGGCTA[A/T]TTTTTTCTATTTTTA | 23607 |
rs544178640 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47583829 | ATTGAGTTTTGTAGG[A/C/T]GCAACTGCCAAACTT | 23607 |
rs544196831 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47613526 | TTTTTTTTTTCCTGA[A/G]CAGTAGGTCTCCACT | 23607 |
rs544203839 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626199 | AAGATGCTTATGAGC[A/G]TGGAAATGTATTTAA | 23607 |
rs544212851 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47571590 | ATATGTAGAGAGCGC[A/G]CCAGAACTGTTCTTG | 23607 |
rs544251626 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47577271 | CGTAATAAGTGCTCA[C/G]AACGTTCTCTTTTTG | 23607 |
rs544258946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47591176 | TGAATCTTAGGATTT[C/T]GTTGACATAAAGTTA | 23607 |
rs544260254 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47585086 | ATCATGAGGTCAGGA[A/C]ATTGAGACCATCCTG | 23607 |
rs544274813 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47527706 | TGCCAGGAAGCTGCT[C/T]GGAGTACGTTGAGTG | 23607 |
rs544293900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47547734 | TATACATTCTATTCA[A/G]CAGTGCATGTTCTTT | 23607 |
rs544295972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47516560 | GTCTTTTCATGATGT[A/G]CAATGGATGCTTTGT | 23607 |
rs544316402 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47480353 | ATGATTTTAGATGCA[C/G]CCTAAAATATTTACA | 23607 |
rs544322680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47598214 | ATACCACCTCACTTC[C/T]GCAAGAATGGCCATA | 23607 |
rs544327170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47478445 | AACTGGTGGGAGAGC[C/T]CGCGGGTGCTTTCCC | 23607 |
rs544330660 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47568083 | GACCTAGTGATAATG[G/T]TATTTGGGGGATGAC | 23607 |
rs544341567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47587277 | GTTCCATGGAAGGTA[C/T]CCTTCGAAAAGCTCT | 23607 |
rs544359717 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47576080 | TATTGTATTTGTTTT[A/T]TTGTAGTTTTTAGAG | 23607 |
rs544372399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47485502 | CTAAATGTTATTACA[A/G]AAAAGTTAAAAAATT | 23607 |
rs544412983 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47561757 | GTGTGAAATGAGTAA[C/T]TGAGTTTGCTTTACA | 23607 |
rs544437875 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47613855 | TCCTGTAGCCAACTC[C/T]CGTCTTAGCTAGATC | 23607 |
rs544440027 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47595782 | TGTCACACTTTTCCA[G/T]CCTGATACAAACTTT | 23607 |
rs544446663 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47567154 | GTGGTTTTTCACTAT[G/T]GTAGTCCATTTGTTT | 23607 |
rs544453837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47510477 | TGGTGGCAGAAAATT[A/G]AGTGGTTAAAAAAAC | 23607 |
rs544458907 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47477981 | CGGGCGGGCGGGGTA[G/T]GGCCCTCCCGCCGCC | 23607 |
rs544481509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47555063 | GTAAAGATATATTTA[C/T]ATGCATTTTTGGTCT | 23607 |
rs544502516 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47507414 | GAGGTTTTCAATTTA[C/T]TTTGCCCAGATTGAG | 23607 |
rs544538422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47589485 | ACACATATACACATA[C/T]GTATGTGCACATATA | 23607 |
rs544540303 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47581723 | TACTGAAAAAATAGA[A/T]TGTTTTCATCACCAC | 23607 |
rs544543195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47554587 | CTTAATTTTCCCATA[A/G]GGTGACGATTTTCAC | 23607 |
rs544549262 | snp | C/T | 0.000177368 | 0.00941554 | intron-variant | CD2AP | GRCh38.p7 | 6:47478294 | TCCGGACCTTCCAGA[C/T]CCGGGGAGGCTGTGC | 23607 |
rs544556968 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47579867 | TATGCTGTTGGTGCA[-/T]TTTTTTTGGGAGGGC | 23607 |
rs544568856 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47531838 | AGCACTTTGGGAGGT[C/G]GAGGCAGGCAGATCA | 23607 |
rs544576186 | in-del | -/CAGCCGCG | 0.00318978 | 0.0398085 | utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47478160 | CGCGGGTCCCGCCTC[-/CAGCCGCG]GGAGCGGCCGCGCGA | 23607 |
rs544597298 | in-del | -/C | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521842 | CCAACGTGGAGAAAT[-/C]CCGTCTCTACTAAAA | 23607 |
rs544597873 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47565804 | TGCTGTATAATTACC[A/G]TAGCCTATATGCCAT | 23607 |
rs544607569 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47539052 | ACAATATTGGTCTAG[A/G]CAATTAATTAAATCT | 23607 |
rs544665913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47580213 | TTTTACTAAAGAATA[C/T]GTTTTTCTGCTTTTA | 23607 |
rs544725207 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47593616 | CACCACTTCACACCC[A/C]CTGAGATGGTTAAAA | 23607 |
rs544791403 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | CD2AP | GRCh38.p7 | 6:47547539 | TTTATAAGACAATTA[A/G]TAATAGGCCTAAGAA | 23607 |
rs544812646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47565082 | CTCTTAATAATATAT[A/G]GACAATGTTGAGTCT | 23607 |
rs544829869 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47509801 | AAGTGGTATTTTGGC[A/G]GACTACAGTAAGATG | 23607 |
rs544847085 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47607861 | ATTTGCTTTATTATC[C/T]AAAGACTTACTACCT | 23607 |
rs544850469 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47612187 | TGTATGATAGCCGAA[G/T]ATAGAAAATTTCTTC | 23607 |
rs544850610 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47604058 | AAGAAAATTGGCAAC[C/G]ATAAAAATCAGTTTA | 23607 |
rs544892963 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47597342 | CTGAACTCCTCCACT[A/G]GCTTTCTCAGGCCTT | 23607 |
rs544924183 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47504594 | TGTTATGTAAATAAT[C/T]GTTATGCAGTATCAC | 23607 |
rs544942565 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47563610 | CAGTATTATGCTCTA[A/C]CATATATTCGTTGTG | 23607 |
rs544967229 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47491824 | ATACTGATTTTTTTT[A/T]AAAAAGTTATTAACA | 23607 |
rs544971191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47594245 | CACTGAATTGTTCAT[C/T]TTAGAATTTTTAATT | 23607 |
rs544971584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47610111 | GGACTTTTTAGAGCT[A/G]AAACAAATTTACAAG | 23607 |
rs544977853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47508301 | GTTAACTTGTTGCAG[C/T]TTCTCTGTCAGCACT | 23607 |
rs545008547 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47485254 | AAAAGGCATTGTTAT[A/C]GTAGGTGATGACAGC | 23607 |
rs545030715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47609468 | GATTGCTTGAGTCCA[A/G]GAGTTCGAGACCAGC | 23607 |
rs545034320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47601426 | TACTACCTTTGGTGT[A/G]CTATACTTAGGCCCT | 23607 |
rs545047519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47515379 | GATCAGAGTGCTACA[C/T]TGAGAGTGGAAATGA | 23607 |
rs545098246 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47593097 | TTGAATTAAATTATA[A/G]GACACTCAGCTGGTG | 23607 |
rs545109951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47508927 | AATTTCCTTCAAGAC[C/T]TTTGTCTTTGTATTT | 23607 |
rs545138980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47499686 | GTAAATAATAAATGA[A/G]TAAAAAGCTAACTGG | 23607 |
rs545160800 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47477075 | TCATGTTTGACTGAC[C/T]ATAGTAATCCTATGC | 23607 |
rs545166971 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47616969 | CTTCTTTTTTTACTT[C/T]TTTAATTTTGTTTTT | 23607 |
rs545176092 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47595192 | ATAAAATTGTCTTTA[A/C/T]TGACATAGTATAAAA | 23607 |
rs545184640 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47510620 | AATACAGCATAAGTA[G/T]ACATGAGTCCATATT | 23607 |
rs545217518 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47612161 | GGCTTTCAGTTTTCC[A/G]ACCTGGAAAATGTAT | 23607 |
rs545223472 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520548 | TTTGTTTTCACCTAG[G/T]GTGGAGGGAAGTCCC | 23607 |
rs545255519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47615870 | CTGCAAGCTCCACCT[C/T]CTGAGTTCACTCCGT | 23607 |
rs545259583 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47512577 | TTTGTGACAAACTTA[G/T]GCCCATTTCATTGTC | 23607 |
rs545319584 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47600701 | TGATAAACAGAAAAA[A/G]AATCCTCATGTTTTA | 23607 |
rs545333650 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47507161 | ATCTGTCCATGTTTT[A/G]TCACAAGGTTGCAAT | 23607 |
rs545365557 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47613795 | AAGTCCTAGATGATA[C/T]CTTCTTTCAATAGAA | 23607 |
rs545365777 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | CD2AP | GRCh38.p7 | 6:47511314 | AGAGACATTCTACAA[A/C]ATACCTGACCAGTAC | 23607 |
rs545414057 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47565830 | GCCATTACCTACTTA[A/C]TGAATAGTCTGGTAG | 23607 |
rs545416064 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47553450 | TTCCCAGGTTCAACT[-/G]ATTCTCCTGCCTCAG | 23607 |
rs545423564 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47514850 | TGAGGTCAGGAGTTG[A/G]TGACCAGCCTGGCCA | 23607 |
rs545429236 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47558944 | TTCGGCTATGAATCC[A/C]TCTAGAGCTGAGCTT | 23607 |
rs545504706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47511950 | GATCACGAGGTCAGG[A/G]GATTGGGACCATCCT | 23607 |
rs545518387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47517897 | GAGATGATGTATTAA[A/G]CGTTTAATCTAGTAG | 23607 |
rs545551160 | in-del | -/AAG | 0.000610606 | 0.0174623 | cds-indel | CD2AP | GRCh38.p7 | 6:47607964 | TCTTGAAGTTACCAA[-/AAG]AAGAAGACAGTGCCA | 23607 |
rs545552940 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624251 | GACCTGGTGTTCATA[A/T]TGTTCCAGGGATTCA | 23607 |
rs545558444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47551873 | GGTTGACTCTCTTAC[A/G]GTGTAGGCATCTCAA | 23607 |
rs545583143 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47529366 | ACGGGTTTTCTCTGG[G/T]TACTCCAGTTTCCTC | 23607 |
rs545644398 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47528849 | CATTTAAAAAATCAG[G/T]CTGTTTGCTTTTTTA | 23607 |
rs545654808 | snp | A/G | 0.00025138 | 0.0112083 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47599355 | AACTGAGCCAGTATC[A/G]AAACTAAAGCTAGAT | 23607 |
rs545656868 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47566691 | CATTGTTCAACTCCC[A/G]CTAATGAGTGAGAAC | 23607 |
rs545698704 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47479358 | GCTGATGTGGCACCC[A/T]CTGTCCACACTTTGC | 23607 |
rs545720362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47573905 | CTGTGTAAATTGCAT[A/G]AATTGCATCTTGCTC | 23607 |
rs545734791 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47593123 | TGGTGCCAGATAATT[A/G]GTTGTTGTGGGAATA | 23607 |
rs545755283 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47605872 | TTGTGATACAGATTT[A/G]TTTTTCACCAAGTAC | 23607 |
rs545778157 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47525720 | CTTTAACTTCCCCCA[A/C]CATTTGCATATGTAT | 23607 |
rs545810819 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47488536 | AGATAGCTTACATTT[C/T]TTCTTATATATGAAA | 23607 |
rs545813544 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47533869 | CAACTACAGTAACTT[C/G]CTGCAAAGTCTCATG | 23607 |
rs545821513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47562808 | AGCCTTTGTATGTCA[A/G]GTTGGTGGAGGCCCT | 23607 |
rs545829329 | snp | G/T | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47477021 | GAAGGGGGAAAAAAA[G/T]CTTGCTGAAATAATT | 23607 |
rs545847408 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47622328 | CTGCAAACCAGATTT[G/T]CCGCCCTACCCAGAG | 23607 |
rs545864841 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47564450 | TACTTTTATAATTAT[A/G]AAATACTTTGCACAT | 23607 |
rs545890024 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47598371 | ACTAAAAGCAGATCT[A/G]CCATTTGATCCAGCA | 23607 |
rs545926588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47555404 | TGGAAATGTAGGGAT[A/G]AGAATATGTTTTTCT | 23607 |
rs545943262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47524930 | TACTGATTTCATATT[A/G]AGGACATTTTTTCTT | 23607 |
rs545964609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47563346 | AATACTTTGTTTGCC[A/G]CTACATTTTGCTTAA | 23607 |
rs545973119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47576293 | TAATATACTATGGAC[A/G]TCAGAGAATATTATC | 23607 |
rs545980290 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47519658 | TGTAGATATATAGTG[C/G]AATTTATTATCTCAT | 23607 |
rs545985456 | snp | A/T | 0.0244538 | 0.107838 | downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47627420 | AGTAGGTTTTTTTTA[A/T]AAAAAAAATGGAGGC | 23607 |
rs546035248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47504715 | TTCAGTTCCAGACCA[C/T]CACAATAGAGCAAAT | 23607 |
rs546092027 | snp | C/T | 0.00333154 | 0.0406776 | intron-variant | CD2AP | GRCh38.p7 | 6:47612437 | AATAAATTATTTAAT[C/T]GAAAGACTTAACAGT | 23607 |
rs546092455 | in-del | -/AGAA | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47612052 | AATTTTTAAAAATAG[-/AGAA]AGAAATTCAAAGTCT | 23607 |
rs546099319 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47548663 | CCTGTTGACACTGTT[G/T]CACAAGATAGAGAGA | 23607 |
rs546126003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47599065 | TTCTGTATACTAATA[C/T]CTGTTGAATGTTAAT | 23607 |
rs546153440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47568788 | ATTTAGATTAGATGA[C/T]CTAGGGAGAATATAC | 23607 |
rs546182833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47566388 | CTAGAATGGTCTCTG[A/G]TATGTTGATGCTCAG | 23607 |
rs546195362 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47497298 | CCCTTTTCCTGTTCC[C/T]GTTCCCTTTTTCCTT | 23607 |
rs546250644 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47572081 | CAGTAACACTCCCCC[A/C]TTGTAATAACCAAAC | 23607 |
rs546258089 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47501733 | AGATGAATGGGGATA[-/T]TGGCTAGTCTGCTAT | 23607 |
rs546259147 | in-del | -/C | 0.00874735 | 0.0655527 | intron-variant | CD2AP | GRCh38.p7 | 6:47580466 | CCAAAACAAAACAAA[-/C]AAAAAAAAAAACGGT | 23607 |
rs546274903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47573983 | TTTATTAGAAGGCAT[A/G]TAGAATGTAGACATT | 23607 |
rs546310081 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47500839 | GCAACCTCCGCCTCC[C/T]GGATTCACGCCATTT | 23607 |
rs546313313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47615010 | ATTCTTTCTGCATAT[C/T]TCAGAGAAAGTTGTA | 23607 |
rs546320750 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47566800 | GATATGATCTCATTC[C/T]TTTTTATGGCTGCAT | 23607 |
rs546325166 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47481723 | GAGTGATTTCTTTAT[A/G]TTACTTTGTTGTACT | 23607 |
rs546386062 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47529509 | CCCTGAATTGGTGGG[A/G]ATAGGCTCTGGCCAC | 23607 |
rs546398518 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47544271 | ATCACTAGCCTAGAG[C/G]ACTTGTCTATGATGA | 23607 |
rs546398535 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47535107 | AGCCTAGAGATTGCA[A/T]ACTTATTACTATGGT | 23607 |
rs546407696 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47558748 | ATTGAGGATTTTCGC[A/T]TTGATGTTCATCAGG | 23607 |
rs546418577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47489464 | TACAGGCATGAGCCA[C/T]CGTGCCCGGCTGCAC | 23607 |
rs546425301 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47557987 | TCCATTTGTTTGGGT[C/T]CTCTCTTATTTCCTT | 23607 |
rs546435861 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47517848 | AAAAAGGGATATTAA[C/T]AGTATTTATCTTATA | 23607 |
rs546458195 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47481182 | GTCAGAGCATTTCTA[C/G]AGCACAAAAAAGGAA | 23607 |
rs546459989 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47556939 | AATTTACACTCCCGT[A/C/G]AACAGTGTACAGGTG | 23607 |
rs546469012 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47499119 | CTTACTTTCTGGCAC[A/G]ACAAAATGTTCCAGG | 23607 |
rs546487349 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47559072 | GTTTATGTGTCCAGG[A/T]ATTTATCCATTTCTT | 23607 |
rs546502509 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47599204 | AACAGAAAGTAATCG[A/G]TATTAGGCCATACAA | 23607 |
rs546544108 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47592484 | AAGGAATGTGCATTT[A/C]ATATTTGTCCCTGGT | 23607 |
rs546552127 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47556137 | CATAGGTATACATGT[C/G]CCATGGTGGTTTGCA | 23607 |
rs546554154 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47478899 | GAGCAGTTTCCTGTT[G/T]GGAGTTAGACTTCCT | 23607 |
rs546578952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47514375 | TAAAACTGAGGAGAA[A/G]CCAGGCTAACTTAGC | 23607 |
rs546593857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47492098 | CTTTGAAACTTTGAC[C/T]GTTTTACTTTAAGTT | 23607 |
rs546598183 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521601 | GCTGTTGTTATTAAG[C/G]TAGTGTTTGGAAAAG | 23607 |
rs546621872 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624407 | TATTTTGTTTTGCCA[A/G]TATGAAGAAAAAGAG | 23607 |
rs546626220 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47528255 | TCTTGGCTCACTGCA[A/C]CCTCCGCCTCCTGGG | 23607 |
rs546639856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47484936 | TCCCCTAAGATTATA[A/G]TGAAGCTAGAAAATT | 23607 |
rs546669949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47609603 | ACTCAAGAGGCTGAG[A/G]TGGGAGGATGTCTTG | 23607 |
rs546703101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47485772 | ATACTGTATTTTTAC[C/T]ATACCTTTTTTATGT | 23607 |
rs546715823 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47508001 | GCTGTCATCTAGGCT[G/T]TGGTTTTCCATTTAT | 23607 |
rs546730957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47494234 | TGTGTTTAATATTTG[C/T]TCTAGCTGTAGGTGC | 23607 |
rs546735301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47575703 | GTTAAATTACTGTTA[A/G]ATAATAAGGTTAAAT | 23607 |
rs546750852 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47616418 | TTTTTAACAGAAGCA[A/G]CCAATCTTCAGAACC | 23607 |
rs546771382 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626451 | GTAAATCATGAATTT[G/T]TTTTCTACGTGTGAG | 23607 |
rs546798079 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47583002 | GTTAGCCAGGATGGT[C/G]TCGATTTGCTGACCT | 23607 |
rs546815924 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476467 | CTTTAGCTTTTTATT[C/T]TTTTGCTTGGTAGGG | 23607 |
rs546832410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47573549 | GCTGGAGTGCAGTGG[C/T]GTGATCTTGGCTCAC | 23607 |
rs546839509 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47621136 | CAGTTCTCAGAGGGA[A/G]TGCTTTCAACTTTTC | 23607 |
rs546849180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47603274 | GTATTGAGTCATATT[C/T]TTATAGTGAGATATT | 23607 |
rs546858940 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47528999 | TGCATGGCAACATCT[G/T]AGCAGTTGCCCAAGT | 23607 |
rs546866391 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47594484 | TTGTGTATTCTGTTA[A/T]AATAAATATATTCAA | 23607 |
rs546870667 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47491295 | TGTGTGTGTGTGTGT[C/G]TGTGTGTGTAATATA | 23607 |
rs546888989 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | CD2AP | GRCh38.p7 | 6:47552142 | GTCTGTTTTTTTTAA[A/T]TTTTTTAATTTTTTT | 23607 |
rs546896725 | snp | C/T | 0.000399281 | 0.0141238 | missense | CD2AP | GRCh38.p7 | 6:47595873 | TAGATGAAAAATCAA[C/T]ACTGGAACAGAAACC | 23607 |
rs546957587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47545724 | CCCCCAGTACCAGCC[C/T]GGAGCCTGGTAGACT | 23607 |
rs546968005 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47481295 | AACTTTTTAGTTTAT[C/T]TTATAGGCTCTCGTA | 23607 |
rs547031903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47481944 | TTAAAATTTTTTTGT[A/G]GATACAGGCTCTCCC | 23607 |
rs547081811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47622008 | ACGCTCTTCTTGGGC[A/G]GGTCTTGCTGTGGCT | 23607 |
rs547089176 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47533495 | AAACTATTGATATTA[G/T]GATTTATATAGTAAT | 23607 |
rs547099536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47531020 | CCTGGGAGGCCAAGA[A/G]GGGAGGATCACTTGA | 23607 |
rs547101200 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625605 | TATGCTTTATTATAT[C/T]GCAAATGAGTGTCAG | 23607 |
rs547110846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47535741 | GGGGGACAAATAACA[A/G]TTTTATATCATACAG | 23607 |
rs547156382 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47564028 | GGTAGGAATCAGTGG[A/G]GAAGGAATCATACCA | 23607 |
rs547162069 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47526690 | CTGAACCTGTCCTCT[A/G]TCACATTTGGTCAGA | 23607 |
rs547162308 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47599942 | GGACTGGTTTTTCAG[C/T]TTACTGATATCTTTG | 23607 |
rs547162816 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47530415 | TTATCTGCTTTTTAA[A/T]CTATACATTAGTTTG | 23607 |
rs547176694 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47552055 | ACTTCTTGGTGGGAG[G/T]AGTGTCAAGGTCACA | 23607 |
rs547196714 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47578346 | GCTGAGACTACTACA[G/T]TTGCATCCCATTGCG | 23607 |
rs547221366 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47590716 | ACTGTACAGTGGGAA[G/T]GTCTTATGTACATGT | 23607 |
rs547246159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47504186 | TTTACACATCAGTTA[C/T]AATTGTCTTGTTTTC | 23607 |
rs547270016 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47555540 | AACCTTAAGGTTGCC[A/C]GTATCATTGGTTTTT | 23607 |
rs547298575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47500848 | GCCTCCCGGATTCAC[A/G]CCATTTCTCCTGCCT | 23607 |
rs547311560 | snp | A/T | 0.0475351 | 0.146656 | intron-variant | CD2AP | GRCh38.p7 | 6:47605977 | ATCAGGTAAAGAGGA[A/T]TTTTTTTTTTCTTTT | 23607 |
rs547314158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47545266 | TATGTTAGGAAAGCC[A/G]AGAGAACCCACAGAC | 23607 |
rs547418423 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47570636 | TTCTCAGTGATACAT[C/T]TTTTAAAGTTTTAAA | 23607 |
rs547423029 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47541521 | AAAAACCTTACACAG[A/T]TGTAACTTTCTTATT | 23607 |
rs547475728 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47597754 | ATGGTGGAATTCTCA[A/G]CCTGGTGCTTTTGAG | 23607 |
rs547494177 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47553961 | GTTATGTTTATTTTC[-/T]TTTTTTCTTTTTTTG | 23607 |
rs547509373 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47506756 | GTACAGTCCAGCTTC[A/G]GCTCCGCATGAGAGG | 23607 |
rs547547474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520033 | GGCAAAACAAATTTT[A/G]TTAGGTCTTTTTTGT | 23607 |
rs547573948 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47516991 | AATGTGATTCCTAAT[A/G]TGGGAGGTGGGGCCT | 23607 |
rs547582889 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47587501 | GCAGTTCTCTGCCCC[G/T]CTGTTGTTTTCATTT | 23607 |
rs547588248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47622364 | GCCTGGAGGTCTCTC[A/G]CCCCGTTCAAATTGT | 23607 |
rs547604326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47498677 | TTTGGAAGACATAAA[C/T]TTTAAAAACTTTTTA | 23607 |
rs547646203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47511702 | CAGCAATGGATAATA[C/T]ACAAATTAATAAGGT | 23607 |
rs547652936 | in-del | -/TG | 0.00478085 | 0.0486577 | intron-variant | CD2AP | GRCh38.p7 | 6:47504190 | CACATCAGTTATAAT[-/TG]TCTTGTTTTCTGTGT | 23607 |
rs547683538 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47512884 | TGATTTAGACACTTA[A/C]ATAATTGTTTCACAT | 23607 |
rs547741079 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47507247 | ATCTACCGTTAACTT[A/C]CCCCACTTAGTCTTG | 23607 |
rs547741577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47557044 | AGATGGTAGCTCATC[A/G]TGATTTTGATTTGCA | 23607 |
rs547747448 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47543943 | TATTCCTGATCATCT[A/C]CCCATAGCTGCTTAA | 23607 |
rs547819435 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47584799 | TCTTAGATCAGTTTT[C/T]AGTACTTGTTTATAA | 23607 |
rs547848072 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47600379 | GTTCAAGGGCAGTTA[A/C]ACTTAGATGTTTTTT | 23607 |
rs547914514 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47496719 | TCTATTCTCATTCTC[C/T]ATAGGGAAACCACTG | 23607 |
rs547949615 | in-del | -/T | 0.00874735 | 0.0655527 | intron-variant | CD2AP | GRCh38.p7 | 6:47540274 | TTGACACCTCTCTTC[-/T]TTTTTTGTGCTTAGC | 23607 |
rs547971047 | in-del | -/ATAGAG | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47612818 | GAAACGATTGAACTC[-/ATAGAG]ATAGAGAACAGAAGG | 23607 |
rs548012942 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47553943 | TTTCTGTGCCATTTA[A/G]GAAGTTATGTTTATT | 23607 |
rs548028228 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47608438 | CCTTTCATCTGTTAC[A/G]TGTGTTAGGTGTCTT | 23607 |
rs548066689 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47565269 | CTTTTAGTATTCAGT[C/G]TCAGGGAAAGCATTG | 23607 |
rs548108231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47530194 | TATCATGAACATTTT[C/T]TAAAATGACCTTTAT | 23607 |
rs548124449 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47581394 | TCCATAATTTTCGAA[-/T]AATTGATCTTTACAA | 23607 |
rs548126888 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47581843 | AGTGGCAGGTCCAGG[A/C]TTAGAAATTGAGCCT | 23607 |
rs548140870 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47564694 | TGTTGTGAATGCCAG[A/G]AAGTGAGCATTATAT | 23607 |
rs548158801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47569023 | GGTTAAGTAAAAGAG[A/G]TCATTAAGGACCTAG | 23607 |
rs548163482 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47552983 | TCATTTCCTTTTGGG[C/G]GGGAGCATTTTTTTT | 23607 |
rs548164307 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47619316 | CATGTCCATGAGAAC[A/G]TACAATGTTTGATTT | 23607 |
rs548195299 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47495731 | TTCTTGTAAGGGTGG[A/G]AGTGATGACTTTAAA | 23607 |
rs548219164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47576440 | CCATTAGGGAAAGCT[A/G]GGTAACTGTAAATGG | 23607 |
rs548219737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47522704 | GTTTCAACCTAAATT[C/T]CTAGCAATTTTTTTC | 23607 |
rs548295185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47569584 | TTAAGAAACCCTGAT[A/G]GATTGTTCTTCAAGA | 23607 |
rs548311171 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47525229 | AACATTTAATTCTTA[C/T]TTTCCTTATTCTTTA | 23607 |
rs548380805 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47538360 | GATTCTCCTGCCCCA[A/G]CGTCCCAAGTAGCTG | 23607 |
rs548384810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47547206 | TCACATGTCAATACT[A/G]ATGTTGAGTGTAAAT | 23607 |
rs548392263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47613219 | CTTTCTCTTATGAAT[C/T]GTGAATGTTCCTCAT | 23607 |
rs548418651 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47560520 | TGACATTTTTGAAGA[C/G]TTTAGGCTGATTATT | 23607 |
rs548458439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47590626 | TTCCACAGTGCTCAC[C/T]ATCGGGTTTGAGTAT | 23607 |
rs548458936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47568170 | TTTGCAGAGATAGGA[C/T]ATTGGGAGATGATGA | 23607 |
rs548463419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47611130 | GGATAAATACTATTG[A/G]TATATTAATAGAGAA | 23607 |
rs548519947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47539204 | CATGTTAAGTAATTG[C/T]AAGTGCTTGATAAAT | 23607 |
rs548520407 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47567658 | TAGATTGAGATCCCA[A/T]AATGGCTAGGAAATT | 23607 |
rs548521628 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47525872 | ATTGACATTACCTAT[A/G/T]GTGCAAGTGGCTTCC | 23607 |
rs548523326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47612687 | TTCAGTCACAAAAAA[A/G]GAATGAGATCCTGTC | 23607 |
rs548550040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47572381 | TATTTAAAACGGGTT[C/T]ATTTTATTCATTGTA | 23607 |
rs548560947 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47517478 | CTATTTTTTGTGGAG[G/T]TGGGGTTTGCCATGT | 23607 |
rs548582121 | snp | C/T | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476664 | CCTTTTGAGAAGCAT[C/T]AGAAGAATTAAAAGA | 23607 |
rs548587605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47531901 | AACATGGTGAAACTC[C/T]GTCTCTACTAAAAAT | 23607 |
rs548610291 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47579723 | TAACCTTAGACTTCT[A/T]TATTTTATAATTTAA | 23607 |
rs548642349 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47588227 | CTATTTAAAAGTAGG[C/T]ATTTCTCATTATTGT | 23607 |
rs548642853 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47496245 | GGTGTAGAGAGTTTA[A/G]GATTTGTAGGTATTT | 23607 |
rs548679570 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47507715 | CTCAGAAAATGCAGA[G/T]ATTACAGGTGTGAGC | 23607 |
rs548681924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47562125 | AGTTATCTAAACATC[A/G]CAAGCTACAATTGTG | 23607 |
rs548689409 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47547580 | AAGACAATAATAGTG[A/G]GGGACTTCAATACTC | 23607 |
rs548695459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47518007 | TGTCAGTTTATCCCC[C/T]TAGGTAGAATGGTTA | 23607 |
rs548697387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47510865 | AGATTACGAGGTCAA[A/G]AGATCGAGACCATCC | 23607 |
rs548703064 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47622949 | GCAGTAGTAGCCTTC[A/G]CACTCCCTACTCCCT | 23607 |
rs548742097 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47478919 | TTAGACTTCCTTGCC[G/T]GAGGAGAGAAAAATA | 23607 |
rs548766352 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47505570 | GACGGGGTGGTGGCT[C/G]GGCAGAGGCGCCCCT | 23607 |
rs548776883 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47502233 | GTGTCTTCAAAGCGA[A/G]CAAGGGAAAAAGTCT | 23607 |
rs548811746 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47589834 | AGTGAACTAGGTTTT[G/T]ATTTAGTTCCTAAAG | 23607 |
rs548827713 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47597440 | GGCTTGATGAGAGAA[A/T]AAAAAAAGCTAATCA | 23607 |
rs548856298 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47495289 | GATTTGAGATGGAGA[C/T]GTAACAGTGGAACAG | 23607 |
rs548872105 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47579220 | CATTCCTGTGGTCCC[A/C]GCCACTTGGGAGGCT | 23607 |
rs548875869 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47592788 | AAGTTACGGAAACTC[-/T]GCATCTCTTCCTGCA | 23607 |
rs548887822 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47482341 | ATATTTTATAGTTTC[A/C]TGTAGAAATGAGCCG | 23607 |
rs548919059 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47495772 | TGTTGGAGCTGAAAC[G/T]GCCAGTTGAGTATTT | 23607 |
rs548932806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47592780 | ACCTGGAGAAGTTAC[A/G]GAAACTCTGCATCTC | 23607 |
rs548987895 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47618464 | TGGGTAGGATCCATG[-/T]TTTTTTTTTATCTTT | 23607 |
rs549006841 | in-del | -/TG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47508545 | CTTTCTTTTTTTTTT[-/TG]TTTTTTTTTTTTTTT | 23607 |
rs549085171 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47493261 | TTTTGTGTTGGGTCT[G/T]TTGGCAATGAATTCT | 23607 |
rs549090994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521547 | GCAGAGTGAGACTCC[A/G]TCTCAAAAAAGAAAT | 23607 |
rs549124957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47593662 | GAAAATAAGTAATAA[A/G]TGTTTGCAAGGATGT | 23607 |
rs549144476 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47569871 | ACTCCTCCTGGTGAG[C/T]AGCTTTGCAAGGAAA | 23607 |
rs549173685 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47538810 | TGAATATTTACATCT[A/G]TTTTTCAGACATGAA | 23607 |
rs549182737 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47491094 | AATGAAATGTTATTA[A/G]TTAATGACATTAAGC | 23607 |
rs549203014 | in-del | -/CTGA | 0.00557542 | 0.0525036 | intron-variant | CD2AP | GRCh38.p7 | 6:47487088 | TGATGAGTATTTTGC[-/CTGA]CTGTTTTGGTGTATG | 23607 |
rs549205649 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47567439 | TTGTACAAAGTCCTG[A/G]GAATACAGTGATCAG | 23607 |
rs549225632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47600851 | CAGATTATTTGCCCA[A/G]TTTTAACTCTGGAAA | 23607 |
rs549243922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47534911 | GCAGTTTTCCCATTT[C/T]AGGCTACTGAGTAGC | 23607 |
rs549250016 | in-del | -/TT | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47594586 | TTCTAGAAATTTAAG[-/TT]TGGCTGGTTGTTATA | 23607 |
rs549253156 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47602667 | CATCCAGGAGTTAGA[C/G]ACTAGCCTGGGCAGC | 23607 |
rs549258304 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47498576 | GCCTTTTCCTTATTT[G/T]CATCTTTTTCTTTGT | 23607 |
rs549266061 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47587008 | CATGAATAAGAAAAA[C/T]GTCAGTGTTTTGCCA | 23607 |
rs549323422 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47588388 | CAATAGGTATATAAT[A/C]CATAGGGAATACTTA | 23607 |
rs549383854 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47531988 | TGAGGCAGGAGAATT[G/T]CTTGAACCCAGGAGG | 23607 |
rs549400738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47594623 | AAATAGCTTTATTTC[A/G]TTATTGATTTCAATT | 23607 |
rs549403311 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47477507 | TCAGCAGAAACCTTT[C/T]GATCCATCTGAGGCG | 23607 |
rs549408246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47545189 | GCAGCTCCCACTGGG[A/G]TAGACAGAGCAGCAT | 23607 |
rs549416960 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47508553 | TTTTTTTTGTTTTTT[G/T]TTTTTTTTTTGGGAC | 23607 |
rs549425042 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47621498 | AAGATACTGGTCTGT[A/G]GTTTTCGTTTTTGGT | 23607 |
rs549439837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47529734 | AGCCTATGCTAAAAT[C/T]GGTTTCCTTGTACAT | 23607 |
rs549479761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47591587 | ATTTATGCACTTGGA[A/G]TCACTCCTGTTTTGG | 23607 |
rs549487575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47496556 | CAGTTATGTGGTGCT[A/G]TAAACATTTTTGCTG | 23607 |
rs549488219 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47546760 | AAGATGAAGGAAAGA[A/G]TCTTAAGAGCTGTGA | 23607 |
rs549504065 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47495159 | CAGAGTAAGGCTTTG[C/T]GTCAAAAAGAGAGAG | 23607 |
rs549505132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47536619 | GTGAAAACTTTTGCT[A/G]TGATCCATTGCTAAG | 23607 |
rs549531882 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47536868 | AGTAAATAAATTGAC[A/G]TGTTTCAGCATCAGA | 23607 |
rs549541179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47598478 | GCAGCACAATTCGCA[A/G]TTGCAAAGTATGGAA | 23607 |
rs549552242 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47558702 | GGATAAGCTTTTTAA[G/T]GTGCTGCTGGATTTG | 23607 |
rs549560199 | in-del | -/TTTTTT | 0.441158 | 0.161117 | intron-variant | CD2AP | GRCh38.p7 | 6:47553514 | ACCACACCTAGTGAA[-/TTTTTT]TTTTTTTTTTTTTTT | 23607 |
rs549588261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47532809 | ATTTGAATTGCATTG[A/G]TATATTACATCAATT | 23607 |
rs549649640 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47540187 | CTCAAAAAAAAAAAA[A/G]AAAAAAGAAAAAAGA | 23607 |
rs549656952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47605947 | GTTAATAAAGTCATA[C/T]ACTAATATAAATGTA | 23607 |
rs549672451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47544429 | GCCTTAATATTTGTA[A/G]TTTGGGGCTTGGGGT | 23607 |
rs549698405 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47562049 | GATTACAGGCGTGAG[A/C]CACTGCACCCGGCTG | 23607 |
rs549763349 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47556596 | TCAGGTGATCCACAC[G/T]CCTCGGCCTCCCAAA | 23607 |
rs549795569 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47488941 | ACGTGTTTATTTTGG[A/G]TGGATGCTTAGAACC | 23607 |
rs549857464 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47601527 | TTTATATCCTCAGTC[A/G]TGTTTTAGGCACAGT | 23607 |
rs549869085 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47487588 | CCAGCTGCTCGGGAG[G/T]CTGAGGCAGGAGAAT | 23607 |
rs549874723 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47505235 | GGTGATGACTCTTAA[C/T]GAGCATGCTGCCTTC | 23607 |
rs549898757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47557011 | GACTTTTTAATGATC[A/G]CCATTCTAACTGGCA | 23607 |
rs549916987 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47518415 | ACTGATATGCTTTTT[G/T]TCATTCTAGATTAGT | 23607 |
rs549977574 | in-del | -/CTT | 0.00755907 | 0.0610114 | intron-variant | CD2AP | GRCh38.p7 | 6:47493171 | TTTATTCCTTCTATG[-/CTT]CTTCTTCATATTGAT | 23607 |
rs550037963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47597897 | GGAGGACTCCAGGGT[A/G]CAGTGGGCCCCACCC | 23607 |
rs550051930 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47511465 | CAGAAAAAGGACATT[A/T]GTGGAAAAATTGATT | 23607 |
rs550108749 | in-del | -/ATTATTACTA | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47580785 | ATTTGTATAATTTAG[-/ATTATTACTA]ATTAGAGTTTATTTT | 23607 |
rs550136465 | snp | A/T | 5.11627e-05 | 0.00505754 | intron-variant | CD2AP | GRCh38.p7 | 6:47554800 | TTTTTAATTGATTTA[A/T]ATAAACTTTATATAG | 23607 |
rs550137751 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47564625 | AGTGGTTGAAGTACA[C/G]TATAATTTTTTTTTC | 23607 |
rs550150986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47607519 | GTGAGGTAATAACTC[A/G]TAGTTTTGATTTGTA | 23607 |
rs550159529 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47563801 | GATGCCCAGTTGCCT[C/T]TCATTTTTAAGTGTT | 23607 |
rs550160077 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47559309 | TTGTTGCCGAGCCTG[G/T]TGTGCAGTAGCATGA | 23607 |
rs550162622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47615309 | ATAAGATTGAAAAAA[A/G]TAGGGTTTGGAATGA | 23607 |
rs550183911 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47614234 | TTGGCTGTTTGGGGC[A/T]AAAGGCCAATCTCTT | 23607 |
rs550189160 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47616954 | CTCCATCTCCTCTTC[C/T]TTCTTTTTTTACTTT | 23607 |
rs550222658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47570742 | CTGTGAAGTTCCCCA[C/T]TTTACAGGCAAAGAG | 23607 |
rs550225290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47552907 | TTCCATGAATAAATC[A/G]TTTATTTTTAAGTTA | 23607 |
rs550252451 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | CD2AP | GRCh38.p7 | 6:47581711 | TCACATGTTGGATAC[G/T]GAAAAAATAGAATGT | 23607 |
rs550252475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47506625 | GCCAACACAGCGAAA[C/T]CCCGTCTCCACCAAA | 23607 |
rs550270014 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47515760 | AGCATTATAAAATTA[A/G]AAGTGCTTTTGATCA | 23607 |
rs550286631 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47552148 | TTTTTTTAAATTTTT[A/T]AATTTTTTTATTTCA | 23607 |
rs550302147 | in-del | -/TA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47501694 | TGTGTATTTTCTTTT[-/TA]GTCAGTCTTGTAGGA | 23607 |
rs550306040 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47567585 | GTGCAATAAATGTAT[A/T]TAAGTGGGCTAATCC | 23607 |
rs550311213 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47529647 | AGTGTTTTGATCTTT[A/G]TTTATAAGTTTGGTG | 23607 |
rs550314229 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47618428 | TACTTATTCTACCTG[A/T]CTTTGAGACTGTAAG | 23607 |
rs550351687 | snp | A/G | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520529 | AGGGGGAAGGAAGGT[A/G]TGGTTTGTTTTCACC | 23607 |
rs550372952 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47578239 | AAGGTCTAGCTTTGT[C/T]GCCCAGGCTGGCGTG | 23607 |
rs550374185 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47621397 | TGGTATGAAACCCAC[G/T]TGATCATGGTGGATT | 23607 |
rs550378809 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47529226 | ACTATGGCAGCATCT[C/G]ATCTTCTGTTAGGTC | 23607 |
rs550400507 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47571499 | AGAAGGCTATGGTTT[G/T]GTTGAGGATTGATCA | 23607 |
rs550402983 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47554115 | ATGGGATTTCACCAC[A/G]TTGCCCAGGCTGATC | 23607 |
rs550406446 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47509287 | TTAAAGATCACTAAT[C/G]ACAGATCACCATAAC | 23607 |
rs550417358 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47584675 | AATGGAAGTTTTTTT[-/A]TATTCTTTTTTTATA | 23607 |
rs550447525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47622334 | ACCAGATTTGCCGCC[C/T]TACCCAGAGTTGTGG | 23607 |
rs550449938 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47522332 | GGACAGTATTTGTTG[A/T]TAAGGGGATTCAATC | 23607 |
rs550461969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47481255 | AGGGCAGAATTTCTC[C/T]TTAATAATTTTAGAT | 23607 |
rs550479705 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47573639 | GACTACAGGCACCTG[A/C]CACCATGCCCGGCTA | 23607 |
rs550481805 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47523156 | ATAGAAATGTATTGA[C/T]GACTTTAATAGAACA | 23607 |
rs550538713 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47575840 | AATGAAGTATAAAGA[A/G]TTTTTTTTTCTCCTC | 23607 |
rs550549661 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47602848 | GAGGTTGTAGTGAGC[C/G]TTGATCATGCCATTG | 23607 |
rs550549702 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47610508 | CTGATTTTATCATTT[A/C]TTTTCCAATTTTAAG | 23607 |
rs550560360 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47498916 | ATATCACAATACAAC[C/G]ATAACATTTAAGAAA | 23607 |
rs550568733 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47523503 | TTCATTGACAATAAG[-/T]AAAAATAAAAATAAA | 23607 |
rs550592722 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47500905 | GGCGCCTGCCACCAC[A/G]CCTGGCTAATTTTTT | 23607 |
rs550608682 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47530445 | GTATTTTCTAAGATT[G/T]TTAATGTACCATATA | 23607 |
rs550617157 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47526543 | TTCTTAGATATGATT[A/G]TGTCCCAGAGAAAAT | 23607 |
rs550630682 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47576006 | CTAGTCCTATTTGCA[C/T]TATTTATATAAAGTG | 23607 |
rs550669337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47596384 | TCCCTCTATCTAACC[A/G]TATGTATTCCTTGAC | 23607 |
rs550772669 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47477399 | GCGCTCGCCCTCCTT[C/T]TGTCCGCCTTTTCCC | 23607 |
rs550791094 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | CD2AP | GRCh38.p7 | 6:47549168 | TGCCTGCTCTCACCA[C/G]TCCTCTTCAACATAG | 23607 |
rs550799794 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47614076 | GCTTAAGGAAATGTT[-/A]ACAGTTGGTTAGATC | 23607 |
rs550805893 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47478758 | AAACTCGCAAGGGGT[A/G]CCTCAAGGACAGGAA | 23607 |
rs550810602 | snp | A/G/T | 0.000342246 | 0.0130778 | utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47478236 | CTTCTCCCCGCGGGA[A/G/T]CCCCCAGCATGGGTA | 23607 |
rs550812015 | in-del | -/CAAA | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47617979 | TCTCAAGGCCCTGCT[-/CAAA]CAATTACCTTCATTA | 23607 |
rs550823634 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47513373 | AGTCTAAGTTATTGC[C/G]TATCTATGTAGGTTC | 23607 |
rs550830517 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47627551 | TGAATACGGTATAGT[A/G]TCCTTTTCTTTGGGG | 23607 |
rs550835290 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47580511 | GCCAGTCTTCCTCTC[C/T]CCACAACCCCAGCTG | 23607 |
rs550861165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47596693 | GCTTCCATATTTTGG[C/T]TGTTGTGAATAGTGC | 23607 |
rs550863556 | snp | C/G | 0.000399281 | 0.0141238 | missense | CD2AP | GRCh38.p7 | 6:47582031 | ACTGATAGCTGCAGA[C/G]AAGAAATATTTTTCT | 23607 |
rs550885056 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624533 | TTTTTTTATTGAAAC[C/T]TGTATTATTTTTAAA | 23607 |
rs550925871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47479481 | CACCTCCCTCCTTTC[A/G]GGTAACTTTCATACT | 23607 |
rs550942832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47486600 | AGGTATTTTTTCCTC[C/T]ACTTCTGGCAAAGAG | 23607 |
rs551003748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47561400 | CTTCCTTACTCTGTG[A/G]TATAAGATATTCCAA | 23607 |
rs551010541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47586202 | AAATGTGAACATTAC[A/G]GTGCAAAAACTGGAA | 23607 |
rs551037875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47562942 | AAGAAATTGGTTGTG[A/G]TTGGGTAGTAGTTAA | 23607 |
rs551066856 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47568438 | TTGATAGTACTTTAG[C/G]TGGTATAAGAAACGA | 23607 |
rs551073469 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47597153 | AAAACACTTGGGGGA[A/G]TTATAGTACAAATCC | 23607 |
rs551073783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47579133 | AGCCAGGCACAGTGG[C/T]TCATGCCTGTAGTTC | 23607 |
rs551088772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47525137 | TTAAAATCTAAATCA[A/G]TCATTTCTAGACTAT | 23607 |
rs551140773 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47485937 | TAGGTTTAAGTACAC[G/T]CTATGATGTTCACAC | 23607 |
rs551183285 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47495128 | AAATTACTCCATTGC[A/C]CTCCAGCCTGGGTGA | 23607 |
rs551256866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47501684 | TGTGTGTGTGTGTGT[A/G]TTTTCTTTTTAGTCA | 23607 |
rs551270776 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47592644 | AAGTCCCTAAGGATG[G/T]GGAGGGGCCTTGTTG | 23607 |
rs551275872 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47511437 | TTTTGGTTTCCTGGA[C/T]TGGATTCTGGAACAG | 23607 |
rs551275923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47489209 | TCTCGCTCTTGTCCC[C/T]CAGGCTGGAGTGCAA | 23607 |
rs551290400 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47548995 | AAAACATTAGACAAA[A/G]TCCAGCATCACTTTA | 23607 |
rs551294476 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47508644 | TCTGCCTCCCAGGTT[C/T]AAGTGATTCTCCTGC | 23607 |
rs551308235 | in-del | -/GAAA | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47595116 | TATTTATGAGCACCT[-/GAAA]GAAAGATCAGGAAGC | 23607 |
rs551399589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47507716 | TCAGAAAATGCAGAG[A/G]TTACAGGTGTGAGCC | 23607 |
rs551403024 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47593946 | TGTATGTTTAATGGA[A/G]TATTATTCAGTCACA | 23607 |
rs551412707 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47497558 | TGGGACTGTAGGTGC[A/C/G]TTATCATTACTCCTG | 23607 |
rs551422326 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47499328 | GTGTGTGTGTGTGTT[G/T]AATATATGTGTATCT | 23607 |
rs551429164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47541609 | CTATTGGTTGCATGT[A/G]GTGTGCTTCTTTTGT | 23607 |
rs551484011 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47499948 | TGGCCAGGCTGGTCT[C/G]GAACTCCTGACCTCA | 23607 |
rs551484612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47543715 | TACCCTTAGGACCTC[A/G]TTTAACCCTATTTAC | 23607 |
rs551524008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47600172 | ATGTTCTTAGTTTAA[C/T]TCTAGGAAGCAGATG | 23607 |
rs551578455 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47526442 | ACCTGAGTTTTTTCT[A/G]TTCATTGTAGACTAT | 23607 |
rs551589501 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | CD2AP | GRCh38.p7 | 6:47555984 | TAGGAAAACATAAAG[A/T]TGGTATAGCAAATGG | 23607 |
rs551623779 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47506562 | CCCGGCACCTCGGGA[A/G]GCCGAGGTTGGCGGA | 23607 |
rs551634159 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47542633 | ATATAAAATCTGCTG[G/T]CACTTTGATCTTGGA | 23607 |
rs551638870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47505102 | TGGCAGGGTCATGGG[A/G]CAATAGTGGAGGGAA | 23607 |
rs551659553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47507309 | TCTGTTTCTTCCAGA[C/T]TCCCATTAATGTTGA | 23607 |
rs551729252 | snp | C/T | 9.91048e-05 | 0.00703865 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47503434 | GTTCCCTGACAATTT[C/T]GTTAAGGTAAGTATT | 23607 |
rs551738069 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47492373 | TTTTTTTTTTTTTGA[G/T]ACAGGGTCTTGCTCT | 23607 |
rs551745960 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47571326 | GAACTGGAGAAAATA[G/T]AGGAAGCAAATTTTT | 23607 |
rs551752718 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47550401 | CTAAAGACCTAATAG[A/G]CAGTTCTCAAAAGAA | 23607 |
rs551782945 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47601752 | AATGTGTGAAACTAG[C/T]CTTTTTAATATGTTT | 23607 |
rs551800439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47551013 | TAAGAATGACACAAT[A/G]GACTTTGGGGCCTCG | 23607 |
rs551858656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47597739 | GGCTTTTGCAAAAGT[A/G]TGGTGGAATTCTCAA | 23607 |
rs551889589 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47544332 | CGGTTTTTTTAGTCT[A/C]AAAAATGGTAATGGG | 23607 |
rs551900952 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47522952 | GTCTCATTGATTTAG[-/A]AAAAAATTCTTTTTT | 23607 |
rs551910645 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47611930 | AAAAAAGGACAACTA[A/T]ATAGAAAGATTAGAA | 23607 |
rs551914223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47513663 | CGGCTAAGTATTACA[C/T]ATTTTTTGGATATTT | 23607 |
rs551917799 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47604950 | TAAAATGCATATTAC[C/T]GAACAGTGATGCCTT | 23607 |
rs551977738 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520791 | CACAGTGGTTATTGT[C/T]TAAGAGCTCTCTGTC | 23607 |
rs552001239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47565314 | TGTTATGTTTCGGTT[C/T]TGTAATGTCTCCTTT | 23607 |
rs552130597 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47601661 | TCCTAGTATTAGTAA[C/T]ATAAAAGTGTTCTAC | 23607 |
rs552153907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47546756 | AGTTAAGATGAAGGA[A/G]AGAATCTTAAGAGCT | 23607 |
rs552184521 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47596992 | CCAAGAAGAATATAA[A/G]CATGTTGAAAGCTGG | 23607 |
rs552218881 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47556551 | ATGGGGTTTCTCCAT[A/G]TTGGTCAAGCTGGTC | 23607 |
rs552276263 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47495327 | AAGATGGAGGTAGAG[G/T]TTGGAGTTACGTAAG | 23607 |
rs552280314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47555877 | TTGCAGCGTCATAGG[C/T]TGTTGTGAGCTATTA | 23607 |
rs552306816 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47532651 | ACATTGTCTAATTCT[A/G]TCGTTATAGTTTTCC | 23607 |
rs552316307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47518079 | GAGGTTCTGAGTGTG[C/T]GTCTTTAAGTGTGTT | 23607 |
rs552332255 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47605257 | GGGTAAAGGAAGGTT[A/G]TATTAAAAATGGAAG | 23607 |
rs552369900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47540038 | AAATACAAAAATTAG[C/T]CCAGTATGGTGGTGA | 23607 |
rs552385635 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47606548 | CAAAGAAAGAACCTG[A/T]TTAATTTATCTTTCA | 23607 |
rs552396901 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47568284 | CCAACTTTTACTACC[A/G]TGTTGGCTATTCACT | 23607 |
rs552414203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47554030 | GCCACAATTGGGCTC[A/G]GCCTCCCCAGTAGCT | 23607 |
rs552441923 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47604268 | AAAGCATTTAGATAT[C/G]TCATGAGTCCAAAAT | 23607 |
rs552471520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47561931 | CCACCACCACACCCA[A/G]CTAATTTTTTTGTAT | 23607 |
rs552499622 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47606042 | AGCACAGGTCAATTT[C/G]TGAGTTCTTCAAAGT | 23607 |
rs552526423 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47586071 | CAATACACAACCAGG[A/G]AAGAAAAATCAGTCA | 23607 |
rs552532944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47561307 | CCTTAGTCCTAGGCA[A/G]TCATAGATCTGGTTT | 23607 |
rs552547832 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47487553 | AAATTAGCCGGGCAT[C/G]GTGGCGGGCGCCTGT | 23607 |
rs552555811 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47569740 | GAAATGGTTGTATAC[C/G]TCGTGTGCCAAAGAT | 23607 |
rs552561134 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47614124 | AAACTTTCCTTCATA[C/T]CAACAATAAGGCTGT | 23607 |
rs552562104 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47600928 | GATCTTTATCACATA[A/T]GTCTTTAAATGTTGA | 23607 |
rs552584797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47526052 | ATGTTAATATGTATG[C/T]TATTTCCTGGCTCTT | 23607 |
rs552584948 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47613437 | TAACATTAATCTCCT[A/T]GTTCATTTCCATCAG | 23607 |
rs552601300 | in-del | -/TAAG | 0.0103295 | 0.0711199 | intron-variant | CD2AP | GRCh38.p7 | 6:47597092 | AAATTCCCAGGGTGC[-/TAAG]TAAGCACTATTCTGT | 23607 |
rs552611672 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47621879 | GTGTCATTCAAGGGA[A/C]CAGCAGTGGGCGGGG | 23607 |
rs552621590 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47613464 | TCAGAGTTCTTGGGT[G/T]ACTAAGGGCATGGTC | 23607 |
rs552624941 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47490387 | AGTTCTATAAAACTT[C/T]ATGATGGCTATTCAT | 23607 |
rs552697169 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47512740 | AACATTACAGATGAG[A/G]TTGAGTTCTCATCAC | 23607 |
rs552725917 | snp | C/G | 1.66333e-05 | 0.00288381 | intron-variant | CD2AP | GRCh38.p7 | 6:47576489 | TTATCTTTATTCTAT[C/G]TTAAAATAGTTTATG | 23607 |
rs552755524 | snp | A/G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47495338 | AGAGGTTGGAGTTAC[A/G/T]TAAGCAAAGGAACAC | 23607 |
rs552790370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47602072 | TTTTTGTTCTAATCT[A/G]TAAAGGATATAAATC | 23607 |
rs552806140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47565512 | ACATTAAACCTCTTT[A/G]AGAATCTCCATTTAG | 23607 |
rs552839139 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CD2AP | GRCh38.p7 | 6:47621291 | GTTTTTTCTGCATCT[A/G]TTGAGATGATATGTG | 23607 |
rs552848504 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47591467 | AATGTTAGGAAAATA[G/T]GTTCAATTAAGAATA | 23607 |
rs552869974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47572514 | TAGATCACTATACTT[A/G]TTAGCATTATATTTC | 23607 |
rs552878466 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47546227 | CTGTGGGAAGTTTCA[G/T]CAATAGAATTGAACA | 23607 |
rs552889877 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47601244 | GTTATTTACTCCCTA[C/T]ATAGTAAACAGAGAC | 23607 |
rs552900273 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47514738 | AATCTTTGAAAAAAT[A/G]TCTTTCAGAAAGGGG | 23607 |
rs552917735 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47479721 | CAGAATAAAATTAAA[C/T]TACTTTGGATGACCT | 23607 |
rs552926244 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47558039 | CTTGAAGAGGTCCTT[A/C]ACATCCCTTGTAAGT | 23607 |
rs552934644 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47499460 | AGGATTGAAAGTAGC[C/T]TTTTCCATATATGCT | 23607 |
rs552936206 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47522468 | TTAAAAAATAAGTGG[A/G]TATGTTAACAGAAGG | 23607 |
rs552945851 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47557425 | TCCTGAATGGTATTG[A/C]CTAGGTTTTCTTCTA | 23607 |
rs552949453 | in-del | -/ATATACCTATGCAGCTATACCT | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47518276 | TGTGAGTTTTGACAA[-/ATATACCTATGCAGCTATACCT]ATATACCTATGCAGC | 23607 |
rs552953155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47608635 | TCAGCAGTCTATTGA[A/G]ATTTTATTAAAGTGA | 23607 |
rs552965051 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47507474 | GCCTTACGAAATGTG[A/G]GCTGGAATTTAGTGG | 23607 |
rs552969772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47617560 | GATAATTTCTGTTGC[C/T]CATATAGTCATATAG | 23607 |
rs552974591 | snp | G/T | 0.000399281 | 0.0141238 | stop-gained | CD2AP | GRCh38.p7 | 6:47607958 | AAAAAATCTTGAAGT[G/T]ACCAAAAGAAGAAGA | 23607 |
rs553030006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47507122 | AAGCCACTTTCTTTG[C/T]TCCTCCATAGGAAGC | 23607 |
rs553061253 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CD2AP | GRCh38.p7 | 6:47550658 | ACTAAAAGTAGAACT[A/G]TCACTTGATCCAGCA | 23607 |
rs553063859 | snp | C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47477628 | GCTGCACCTGGACGC[C/G]GTCGGCGCGCGACCC | 23607 |
rs553107441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47529816 | GAATTTACTGTATTT[C/T]AGATTGCCTACCCAG | 23607 |
rs553156391 | in-del | -/AAACAAAC | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47487690 | CGAGACTCTGTCTCA[-/AAACAAAC]AAACAAACAAACAAA | 23607 |
rs553181964 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47548722 | GCTAGTATCATCCTA[A/T]TACCAAGACCAGGAA | 23607 |
rs553182489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47594805 | TAAGTGGTAAAAGTG[A/G]GAAAATAGTATTTTG | 23607 |
rs553186515 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47587483 | TTTTCTCAAACCTGC[G/T]TAGCAGTTCTCTGCC | 23607 |
rs553215389 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CD2AP | GRCh38.p7 | 6:47561642 | CTTGATCATTCATCT[A/G]TTTATCCATCTTTAC | 23607 |
rs553222388 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47622714 | CAGGTCCTGCAAGAG[A/C]AGTCCGCTTTCTTCA | 23607 |
rs553253851 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47583586 | TTCTCCGTATGTTTT[A/C]ATGGCTTGGGAGGCA | 23607 |
rs553327462 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47510121 | AAAAGTTTAATCTGG[A/G]ATTAAAAATTAACCA | 23607 |
rs553347514 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521983 | TCATGCCATTGCACT[C/G]TAGCCTGGGCAACAA | 23607 |
rs553387492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47566635 | TCCTCACCCCTCAAC[A/G]GGTCCTGGTGTGTGT | 23607 |
rs553391788 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47555073 | ATTTATATGCATTTT[C/T]GGTCTGCTGAGTTTG | 23607 |
rs553402371 | in-del | -/TTAT | 0.00993419 | 0.0697739 | intron-variant | CD2AP | GRCh38.p7 | 6:47542844 | TAGCACAAAAGAAGA[-/TTAT]TTAATTTAGAAAGCT | 23607 |
rs553463196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47559886 | TCTAGATATAGAGCT[A/G]GAAAGTCCTAGTACA | 23607 |
rs553466677 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | CD2AP | GRCh38.p7 | 6:47480687 | CAGTGCTGGCGGTGG[G/T]GATTTTCATTTTCAA | 23607 |
rs553499133 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47517870 | TATCTTATAGTGTTA[G/T]GAGTATCCAATGAGA | 23607 |
rs553526573 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47567091 | ATTTCCCAGTTTTTT[C/T]TTTTTTAACTTTACT | 23607 |
rs553531189 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47576897 | AAATTTAAAGATAAT[A/T]AAGTTCATCTCTAAT | 23607 |
rs553542252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47487646 | AGTGAGCTGAGATCG[C/T]GCCACTGCACTCCAG | 23607 |
rs553587337 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47597960 | CTTCTTACCACATGC[A/C]GCAGTAGTCAAGGAA | 23607 |
rs553589990 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47530986 | ATGGGTTTTGGCTGG[A/G]CAAAACTAGTACCAG | 23607 |
rs553592868 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47558340 | GCCTGATTGCCCTGG[C/T]CAGAACTTCCAATAC | 23607 |
rs553679715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47487159 | TCATTTTTACTTACC[C/T]ACTAATTTGGCCATT | 23607 |
rs553712862 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47577608 | TTGGAATAAATCCTA[A/T]TGCAAAATAAAGAGA | 23607 |
rs553716784 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47539832 | TAGAAGACAATTTTT[A/G]TACAATTAATTTTTT | 23607 |
rs553744205 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47536218 | TTATTTTATGTTTAT[A/T]AAACTTGATTTTTTT | 23607 |
rs553753523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47541786 | GTGAAATAACTAGGT[A/G]ATGACAACTGTACAA | 23607 |
rs553776171 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47584932 | TCATGTCACCAGTTA[C/G]TCAGCAGTTTTGTTA | 23607 |
rs553777673 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47600582 | GGATGAAGCTATATT[G/T]ACTACTAATTTCTGG | 23607 |
rs553787043 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47569327 | ATTATGGCTATTATG[A/T]TTAGTCTCAATTTAT | 23607 |
rs553804216 | in-del | -/AT | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47615006 | CATTATTCTTTCTGC[-/AT]ATCTCAGAGAAAGTT | 23607 |
rs553855024 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47585617 | TTAGGAAGGCCCGGG[A/C]AGCTACAATTTGTGG | 23607 |
rs553860486 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47563269 | GTATGCTAATAGTAT[A/C]AAATGACTTGCGTTA | 23607 |
rs553882036 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47542784 | TGCTAGGTGCTGGGT[C/G]GATTGCAGAAGCGAA | 23607 |
rs553889515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47533854 | TCAGTCTTTTGTAGA[C/T]AACTACAGTAACTTC | 23607 |
rs553908381 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47611616 | AATTTTTTCTTTTTT[A/G]CTTTTTCAAGCTGTT | 23607 |
rs553923948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47570009 | ATATTGATTGATTTT[A/G]AGTCCAGTTAAAACA | 23607 |
rs553965594 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47503667 | ATATGCTTGTATATG[G/T]TTGTGTGTATCTACC | 23607 |
rs553971280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47590302 | TATGAATATGAGTCA[A/G]TCTAAGCTTAAATGA | 23607 |
rs553986628 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47578924 | AGCCTCCTAAAATGC[G/T]GGGATTACAGGTGTG | 23607 |
rs554005644 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47538817 | TTACATCTATTTTTC[A/G]GACATGAAATACCTA | 23607 |
rs554008187 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47512223 | GACATGCGCCTGTAG[A/T]CCCAGCCACCCAGGA | 23607 |
rs554033877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47504678 | TTATTCTGCTACAGG[A/G]GTACCTTGGAGATAC | 23607 |
rs554064106 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47496064 | CCACTTCTTTTGTTT[A/T]TCCTTTCTTTTCTAC | 23607 |
rs554065004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47556208 | CTATCCTTCCCCTTG[C/T]GCCCCCCTCACCCCC | 23607 |
rs554073396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47497152 | ACCATGTCGTGTTTT[C/T]TTTTTACTGTGAAGC | 23607 |
rs554093491 | snp | A/G | 6.63163e-05 | 0.00575793 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47606253 | TGGAAGAAGGTTGCC[A/G]GGCCGTTTCAATGGT | 23607 |
rs554204855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47497703 | ACAGGTGTGAGCTGC[A/G]ACTGCACCCGGACAA | 23607 |
rs554240120 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47592448 | ATAGGTTTTTAGATA[C/T]GTGTGATATTGTGAT | 23607 |
rs554249220 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47579610 | GTTTCAGATGTAGCT[-/A]ATTCAGGTAGGAGTT | 23607 |
rs554334399 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47489422 | CTCAGGTGATCTGCC[C/T]GCCTCGGCCTCCCAA | 23607 |
rs554334945 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47501039 | GGCGTGAGCCACTGA[C/G]CCTGGCCTGTGTTTT | 23607 |
rs554366270 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47614610 | GAAAACATTTGAAAT[A/G]TTGTGAAAATTGTCA | 23607 |
rs554402529 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47552397 | TGAGAACATACGATG[A/T]TTGGTTTTCCATTCT | 23607 |
rs554444308 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47505384 | CCAAGACAGAGGAAT[G/T]TTTCTTAGTGCAGAA | 23607 |
rs554459446 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47609531 | AAAAAAAAAAAAAAA[-/A]GAAAAGAAAAGAAAA | 23607 |
rs554462067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47551556 | TAGGTATTTTTATCC[C/T]CATTGTACATAGGAA | 23607 |
rs554479080 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47556616 | GGCCTCCCAAAGTGC[C/T]GAGATTACAGGCGGG | 23607 |
rs554518768 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47545422 | TTTCCTACCCACCCT[A/G]GTAACTGATGACAAA | 23607 |
rs554529346 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497188 | AGTACATATGATTAT[A/G]TTTTTCCTTTCCCCT | 23607 |
rs554577509 | snp | C/T | 0.000399281 | 0.0141238 | missense | CD2AP | GRCh38.p7 | 6:47595999 | AGCGACCTGAAAAAC[C/T]AGTTCCTCCACCACC | 23607 |
rs554584362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47559640 | TTGATAAAAGATTTC[C/T]AGAAATCATTAAGAT | 23607 |
rs554598153 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47494459 | TTTTTTAGTGGATCG[A/T]TGTCCTGGAGCTGTG | 23607 |
rs554606042 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47490974 | TGAGAAAATAAATGA[C/T]GGAATTTCTAATATA | 23607 |
rs554619781 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47529899 | ACCACCCTTATCATC[A/T]TTCCCTTCCTTCCAT | 23607 |
rs554641205 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | CD2AP | GRCh38.p7 | 6:47595709 | AAATATAACTTTAAA[A/T]TAAGTAAAACAGTGC | 23607 |
rs554647090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47561464 | AATCAGCTACCTATC[A/G]AGGCAAACTTTTTTT | 23607 |
rs554659661 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625134 | TATTTTACAGCCTCA[A/T]ATATTTCTCATTATC | 23607 |
rs554665816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47587902 | GTAGAAGCAGTGAAT[C/T]TGCTCACTTTTGCTT | 23607 |
rs554667932 | snp | C/T | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521334 | AGGCGGGCAGATCAC[C/T]TCAGGTCAGGAGTTT | 23607 |
rs554678395 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47488168 | TGATTACCTACTCCG[G/T]GTGTATAAATAAAGG | 23607 |
rs554681265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47537053 | GATTTTTCATGTAGT[C/T]AATTATTTTGAGTGT | 23607 |
rs554725866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47575207 | TTCTTGGTTTTAAAG[A/G]TAAAGTTTGGAATTC | 23607 |
rs554735478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47493599 | GGATGTGTGGTTTGG[C/T]GTACCTTATTATTTT | 23607 |
rs554753033 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47500572 | GTATTATAGTTAAAG[G/T]TGGTTAATCTAGCAG | 23607 |
rs554753810 | snp | C/T | 0.00304413 | 0.0388947 | intron-variant | CD2AP | GRCh38.p7 | 6:47606328 | TTAGCAAATGCAGAG[C/T]CCATTGGAAGATAGA | 23607 |
rs554763303 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47502830 | TGTCTGCCTCGGCCT[C/T]CCAAAGTGCTGGGAT | 23607 |
rs554764259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47602289 | TCATATATAATGTAG[C/T]TTTATAAATATCAGA | 23607 |
rs554773115 | snp | A/C | 8.36491e-05 | 0.00646665 | intron-variant | CD2AP | GRCh38.p7 | 6:47609352 | ACTTAACCCATGCAT[A/C]AAGAATTTTTTTCAA | 23607 |
rs554790802 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47518052 | AAACTTTTGTGTCAG[G/T]TGTTGTTGGGGGAGG | 23607 |
rs554791881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47566613 | TCTCAATTCTCCCTT[C/T]CCCCGCTCCTCACCC | 23607 |
rs554799760 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47578867 | TCACCTTGTTGGTCA[G/T]GCTGGTCTCAAACTT | 23607 |
rs554850886 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47537930 | AATTTTTTCTATTTT[C/T]AGTAGTGATGGGGTT | 23607 |
rs554862735 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47567984 | TTGATAATGAGGTAG[A/T]ATTAGCCTAAACTAG | 23607 |
rs554862887 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47575934 | GGACAGATGACTTAT[A/C]CAAATTTGTATTATT | 23607 |
rs554902210 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47602891 | GGTGATAAAGTGAGA[A/C]CCTGTCTCAAAAATA | 23607 |
rs554970706 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47509648 | TTCTTTTTTTGATCT[A/G]TAATAGATTGTCATG | 23607 |
rs554979605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47478308 | ACCCGGGGAGGCTGT[A/G]CCCTTTCTCGGCCTT | 23607 |
rs555001071 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47555450 | TGTAGTGAGAATTTT[C/T]GGGGATTTGCATTAG | 23607 |
rs555004813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47554821 | CTTTATATAGCATCT[A/G]GTGTTTTATTTTGTA | 23607 |
rs555020517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47505485 | TCCCCGCCTTTCCCG[C/T]CCTTCTATTCCACAA | 23607 |
rs555037987 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47616530 | GTGAAAGTACTTTGT[A/G]AATTATCAGACTTTA | 23607 |
rs555045512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47605168 | ATTAATACAGATCTG[A/G]ACGATTAGACCAAAG | 23607 |
rs555058789 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47546929 | CCAGCAAAACTTAGC[A/T]TCATAAATGAAGGAA | 23607 |
rs555094065 | snp | A/T | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47477000 | GGAATTGGGTCTACT[A/T]AAACAGAAGGGGGAA | 23607 |
rs555108653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47578567 | TAATTTTTAGTATAT[A/G]AAGTGTTAAAAGTGT | 23607 |
rs555110925 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47564142 | GTGTGTAAAAACCAT[G/T]AGAGAACATACATAA | 23607 |
rs555114075 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47585089 | ATGAGGTCAGGACAT[C/T]GAGACCATCCTGGCT | 23607 |
rs555148068 | in-del | -/AAAC | 0.0482004 | 0.14757 | intron-variant | CD2AP | GRCh38.p7 | 6:47487694 | ACTCTGTCTCAAAAC[-/AAAC]AAACAAACAAACAAA | 23607 |
rs555227994 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47611460 | TATTTCTTTACTTGG[A/T]GTTCAGAGGTTTTCG | 23607 |
rs555228425 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47609874 | TGGTCGGATATGATT[A/C]GTTTTTAAACTACTA | 23607 |
rs555272847 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47618905 | TAAAAGCACACCTAA[C/G]GCACTAAAGTTTTAG | 23607 |
rs555287925 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47516249 | GCTTTTCATGTGGCG[G/T]CACAACCTTCTGGGC | 23607 |
rs555289820 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47607562 | TTGTTGTGAAATATT[A/C]ATTGTTTTTGTAGTA | 23607 |
rs555291971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47619557 | TCTTTTTCGAATAAT[A/G]ACTTCTTTTCCTCTG | 23607 |
rs555299735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47513085 | GTAATAAAGATTGTA[A/G]GATTATGACTTCAGC | 23607 |
rs555317371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47606884 | TGACTAGTAGTTACC[C/T]TGATGCTACCAAATA | 23607 |
rs555330831 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626599 | TATTTTTTGTTTGTG[A/G]CCACTAAGCTTCTGT | 23607 |
rs555351401 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47523869 | TAAATCACAGACATA[C/G]TATATGTTGAAACAA | 23607 |
rs555356234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47623164 | CTGAAATTAATAAAC[A/G]GTTCTTGAGTAGTTA | 23607 |
rs555400675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47622161 | CTCACCCAGCTCCCA[C/T]GCAAACTGAAGGAGC | 23607 |
rs555424517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520290 | AATATTTATAACAGT[C/T]AATATTGGTTGAGGA | 23607 |
rs555459739 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47549966 | AAGTGGGGAAAGGAC[A/T]TCCTTTTCAACAAAT | 23607 |
rs555460148 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476846 | AAATGGCTGTGCTGA[A/G]TTTCAAGGACCCATG | 23607 |
rs555460497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47557276 | CCCATTCTGTAGGTT[A/G]CCTGTTCACTCTGAT | 23607 |
rs555469249 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47624139 | GTAAAATAAACTACT[A/T]AACTAAGGATATTTT | 23607 |
rs555485608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521278 | CATAGTAGGCCAGGC[A/G]TGGTGGCTCACACCT | 23607 |
rs555490450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47536040 | GGAAAAATCATTATG[C/T]AGTTGGTGCCAGGAA | 23607 |
rs555503871 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47575559 | CCACAATATGGTGTT[G/T]AGAGTTGGGGAAAAC | 23607 |
rs555545845 | in-del | -/TA | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47518102 | GTGTGTTTATATGTG[-/TA]TATATATACTGGGGT | 23607 |
rs555566692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47585559 | AGGAGGAAGCCAAAC[A/G]GACCTCGATGTCCTA | 23607 |
rs555584939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47565631 | AAGGAGAAATTCATC[C/T]TTCTTTTACTCAGGC | 23607 |
rs555607423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47616791 | CTTCAATTCAGTCTG[C/T]AACCCCTTGCATCTT | 23607 |
rs555608218 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47526336 | CAGCAAACTTTACCT[G/T]ATTTGTAATTTTGCC | 23607 |
rs555624178 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47622594 | AGTTGGAAACTTCTG[C/T]AAACAGACCTTCAGT | 23607 |
rs555652310 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47586669 | TAGAACTGTATTACA[A/G]AAAATGTTAAAAAAT | 23607 |
rs555656502 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47481422 | GCGATCTCGGCTCAC[C/T]GCAACCTCCGCCTCC | 23607 |
rs555671845 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47499331 | TGTGTGTGTGTTGAA[A/T]ATATGTGTATCTGTG | 23607 |
rs555683292 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47527671 | GGTATGGGACATGGA[A/C]GTAACTATGTTGTCA | 23607 |
rs555683469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47519488 | ACTTCTTTTGATGAC[C/T]GTGCCCTTGCCACTA | 23607 |
rs555715033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47507359 | GAATCACAGATGTTA[C/T]TAATGGCTTCTAGAA | 23607 |
rs555717277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47593306 | GAAAGTAAAAAGACA[A/G]CTTACAAAATGGGAG | 23607 |
rs555744642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47527009 | TTATGTGCATTACCA[A/G]TAAAAACAGGGAAAT | 23607 |
rs555807943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47478660 | ATAAAGTAGCACTTT[C/T]AACTTCTTTATTTTC | 23607 |
rs555820662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47617420 | AATTCGTATTTTCCC[A/G]GCTTGTATCCTGTGT | 23607 |
rs555823993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47525508 | AGTCTATGGAATACA[A/G]GTAAATTGCTTTCTA | 23607 |
rs555851859 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476055 | TAAGGGCTCTGGGCC[A/T]TGAATTTACTACCTA | 23607 |
rs555861410 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47503116 | TATTCAAGAAATTTG[C/T]TGATGTAGCCAAATA | 23607 |
rs555899962 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47515311 | ATAAATTAATCTGAA[C/T]GAGAAGGAAAGGTTT | 23607 |
rs555901115 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47594014 | TAAACTGCTAAAACA[C/T]TGGGCTAAGCGAAAG | 23607 |
rs555939505 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47540248 | ATGGACTTAATTTCA[G/T]GTATCCTTTTATTGA | 23607 |
rs555945271 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47487000 | GTTTATTTAGAAGTA[C/T]GTTCTCCTGAGATCC | 23607 |
rs555954831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47604468 | AGTTTCATTTTTCTT[C/T]GTCTTTTCCTGTGTT | 23607 |
rs555974755 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47483458 | CAGTAGGCCTTGAAA[A/G]CCTAGCCACAGGGAA | 23607 |
rs555991907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47543198 | AAAGAAAAAAAAGAA[A/G]AAGAAAGCTATTTGG | 23607 |
rs555992156 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47550541 | TTAAAAAAAAAATAG[A/T]TGTTTGTGTGAATGT | 23607 |
rs556015677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47587351 | CCATGAAACTGATCA[C/T]CCCTCTATTTTGGAC | 23607 |
rs556035444 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47597154 | AAACACTTGGGGGAA[A/T]TATAGTACAAATCCA | 23607 |
rs556072581 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47494723 | ATTCTCCTAGGAGTT[C/T]CCCACTTTCATGCTA | 23607 |
rs556121534 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47572238 | ATATCAAGAAGCAGG[A/G]GCCGGGCGCAGTGAC | 23607 |
rs556156160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47538575 | TTTTAAAAATTGACT[A/G]ATTAAATAAATTTTA | 23607 |
rs556163701 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47584203 | TTGTTTTCTTCACAG[A/G]GCAGAAGTTTTAAAT | 23607 |
rs556172585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47590078 | GTAAATCTTTTGTGT[C/T]TTGTACTCATTCAGA | 23607 |
rs556188684 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47622533 | CTGCTTCCTCTACCC[A/C]CCTTGTATTTTGCTT | 23607 |
rs556207951 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47517209 | CCATGATTGGAAGCT[C/T]CCTCAGGCCCTCACC | 23607 |
rs556228490 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47568627 | TGTGCACCTGTAATC[A/G]CAGCTACTTGGGAGG | 23607 |
rs556235840 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47591758 | TTTGGTTATTTTGTT[C/G]TATTTTGTTAGCATA | 23607 |
rs556262511 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47614824 | TTTTCATTCTTTCTT[C/T]GCTCAGGGACAGGAC | 23607 |
rs556266303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47502382 | TCCTGGGTCAAGCAG[C/T]GCTCCAAAGTAGCTG | 23607 |
rs556275937 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47589527 | GTATGTACACACATA[C/T]ATACACATATGTACA | 23607 |
rs556298222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47576725 | TTCTATTAGATGTAA[A/G]CACCATGAGGTCAAG | 23607 |
rs556307746 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47536714 | TTTCTCAGGAAAAAG[C/T]TGATTACTGTAAGTT | 23607 |
rs556320928 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47486439 | AAACGAGAGAGAGAG[A/T]ATAGGGTCAGTGTCA | 23607 |
rs556337284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47596220 | ATATATAATTCATTG[C/T]GGAATGGCTTCGGTA | 23607 |
rs556359075 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47517728 | GGATATAGACAATCT[C/G]GTATATAGTTTAGGT | 23607 |
rs556374655 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47585101 | CATTGAGACCATCCT[A/G]GCTAACACGGTGAAA | 23607 |
rs556410517 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47483463 | GGCCTTGAAAACCTA[A/G]CCACAGGGAAACAAA | 23607 |
rs556424183 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47597964 | TTACCACATGCAGCA[A/G]TAGTCAAGGAATGGC | 23607 |
rs556424257 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47568202 | GTATCGTTAAAATAG[A/T]TGCCTAGATATTGAA | 23607 |
rs556436919 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47511104 | AAAAAAAAAAAAGGA[A/G]TAGATGGACAGGGAA | 23607 |
rs556441709 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | CD2AP | GRCh38.p7 | 6:47611814 | AAAACCTCGATATTT[G/T]AATACCAAATCACAA | 23607 |
rs556456096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47537951 | TGATGGGGTTTCACC[A/G]TGTTGGCAAGGCTGG | 23607 |
rs556460802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47555077 | ATATGCATTTTTGGT[C/T]TGCTGAGTTTGCAAA | 23607 |
rs556489492 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47595314 | AATTCTTAGTGCAGT[A/C]CTAAGAATTACAAAT | 23607 |
rs556521056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47569267 | AAGAATGGTGGTTAT[C/T]AGCACAATAGAATTT | 23607 |
rs556551899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47504565 | TTAACTTATAATACC[C/T]AGTAAAGTGTAAATG | 23607 |
rs556582986 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47592936 | AAACCCAAGGAGTGA[C/T]CATGGGAATCCCCAA | 23607 |
rs556591850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47488827 | GCCTGGAAGGTCGAG[A/G]CTACAGCGAGCCATG | 23607 |
rs556595104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47541668 | TTGTCTTGATAAACA[A/G]TTTCGTAGATTCACA | 23607 |
rs556609493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47592287 | ATTCTAGTACTCACA[A/G]CTGGATGTTCTCAAA | 23607 |
rs556611407 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47602718 | AACATAGTGAGACCG[A/T]GTCTCTACAGAAAAA | 23607 |
rs556611816 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47598925 | ATAATCTAAAATAAT[A/T]AAAAAAATTTAAAAA | 23607 |
rs556616849 | in-del | -/AAAA | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47525008 | TAATTTAATCATAAT[-/AAAA]AGGAAAATCAAATGA | 23607 |
rs556641667 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47549418 | CCAACAGCAGTCATG[C/T]GGAGAATCAAATCAA | 23607 |
rs556662560 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47481275 | TAATTTTAGATAAGG[C/T]GGTGAACTTTTTAGT | 23607 |
rs556674648 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47489372 | GTAGAGATGGGGTTT[A/C]ACCATGTTGGCCAGG | 23607 |
rs556726292 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47497138 | TTCACATTATTATGA[C/G]CATGTCGTGTTTTTT | 23607 |
rs556773651 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47595680 | TTTTAAAGTTATTTA[A/G]GATTATTAAATTAAA | 23607 |
rs556792904 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47550271 | GCAGAGTAAACAGAC[C/G]ACAGAGTGGGAGAAA | 23607 |
rs556800667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47550739 | TGCACACACATGTTT[A/G]TAGCAGCACAGTTCA | 23607 |
rs556831912 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47563217 | AGTCCAGAGGTGCAA[A/G]TATCACATCTCTAGG | 23607 |
rs556853875 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47581773 | ACGGTAGAGGATATG[A/T]TCTCTAACACCTAAA | 23607 |
rs556855974 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47547844 | TCACACCACAGCGAA[A/C]TAAAACTGGAAATCA | 23607 |
rs556866841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47595002 | ATTATTCAGTATGGT[A/G]CTTAGGAGCTTCTTA | 23607 |
rs556871558 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47606099 | TGTCCAAAAACTGAA[A/C]CATTATTTTTTACCT | 23607 |
rs556889714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47503795 | ACAGTATACTTGTGA[A/G]ATAGTTATGACAGAT | 23607 |
rs556934874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47605642 | TATATACACATAAAG[A/G]TACATTAAATCATGC | 23607 |
rs556953576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47601441 | ACTATACTTAGGCCC[C/T]GTAAAGTTCAGAAAA | 23607 |
rs556967932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47514433 | GTTTTAGACTAAAGT[A/G]GAGAATAAAGATTTA | 23607 |
rs556974472 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47575151 | CCTACATATTCCTAG[C/G]TCTGAGACTATCTGG | 23607 |
rs557011268 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47603580 | CTTTGAAAGACAAAG[C/G]AATAAACCTAAAACC | 23607 |
rs557027185 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47516186 | AGCACAAGGAAAGAC[G/T]ACATCCTTTCATGCA | 23607 |
rs557064990 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47499690 | ATAATAAATGAATAA[A/T]AAGCTAACTGGGAAC | 23607 |
rs557070925 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47611407 | GGATTAAGGAAAGAG[G/T]GTCGCTTTTTGGGAT | 23607 |
rs557094846 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47565600 | CCTGCTCCATGTAAT[C/G]TTCCCCATCTGAGTT | 23607 |
rs557115598 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CD2AP | GRCh38.p7 | 6:47559935 | AGAGAAACCTAAGTC[A/G]TGATTTACATATTAT | 23607 |
rs557119866 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47477694 | GGGGACCGGGAGAGA[C/G]CCCGAACGCGACGGG | 23607 |
rs557128211 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47500460 | AAAATTTCTTGCCGG[C/G]TCCCTTATCATGTTG | 23607 |
rs557137717 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521178 | GTAATGCACATCCAT[A/T]ACAGTTGCTTATCTT | 23607 |
rs557158528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47580979 | ATTGGATCTAATGCA[A/G]ACTATTGATTTTTAT | 23607 |
rs557162308 | snp | A/C | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521388 | GAAACCCCGTCTCTA[A/C]TAAATATACAAAAAT | 23607 |
rs557162845 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47588694 | GATTCTGTTATGGAC[C/G]TGAATTATATCTTTC | 23607 |
rs557167876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47509495 | CGAAGTGCAGTAAAA[C/T]GAGGTAGGCCTGTAA | 23607 |
rs557256574 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47477112 | TCACATTGACGCTAG[A/G]AAAAATGCCTGGCAG | 23607 |
rs557271367 | snp | A/C | 1.64906e-05 | 0.00287142 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47609287 | GTGCATTGTAGAAGC[A/C]CTGAAAAAGGATCAC | 23607 |
rs557274132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47537014 | ATTTTCCTTAGTAGT[A/G]GAAACTCACGCTACA | 23607 |
rs557276869 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47508983 | CTAGCTTTTGGCCTA[C/T]CTCAACTTTCAGCAT | 23607 |
rs557281047 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47543189 | AAAAAGAAAAAAGAA[A/G]AAAAAGAAAAAGAAA | 23607 |
rs557313709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47567633 | AAGGAATGTGCCCTA[A/G]AAGAAGTCATAGATT | 23607 |
rs557329950 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47613093 | TCCACTTTTAATTCT[C/T]ATTGTCTTGCTGTTT | 23607 |
rs557331093 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47500490 | GGGATGTTTTCAGCT[A/G]TAAATAGAAATCCTG | 23607 |
rs557333673 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625710 | TTTAATCTTATAATA[C/T]AGAAATCTTATGTAA | 23607 |
rs557334325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47613853 | TTTCCTGTAGCCAAC[C/T]CCCGTCTTAGCTAGA | 23607 |
rs557343427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47515415 | ATAGATAATAGGCTA[A/G]TAACACTTTATATCT | 23607 |
rs557377480 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47564829 | CCTCGTAGCTGTTAG[A/G]AAAATTATAGTAGAA | 23607 |
rs557392818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47484999 | CTATAGTAGTGCAAC[A/G]CGTTACTCACTGTGT | 23607 |
rs557408020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47523727 | ACAGGTAATACTAGA[A/G]AATATATATAAGGAT | 23607 |
rs557410661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47607011 | ATCTTTCTGTTCTCT[A/G]TCTCCATTAGTTCAG | 23607 |
rs557423281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47511995 | AACCCCGTCTCTACT[A/G]AAAATACAAAAAATT | 23607 |
rs557451018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47553272 | TTTTAAACAAGAAAT[A/G]AATCTTTTTCTAGCT | 23607 |
rs557497208 | in-del | -/AT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47533096 | AAAGGATAATATGAC[-/AT]ATAAAATTATTTGAA | 23607 |
rs557504236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47560979 | ACTTTTGTCTTTCTC[C/T]GGTTTATGTATTTAT | 23607 |
rs557507119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47570174 | TTCAGTGCAGTTCAC[A/G]TGTGGTTTCTTGTTT | 23607 |
rs557571064 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47557705 | TTTTTTGGTACCAGA[C/T]CATGCTGTTTTGGTT | 23607 |
rs557588363 | snp | A/G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47618782 | CTTTTGGATAATTCA[A/G/T]TATGATTTTATTTTT | 23607 |
rs557594902 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47618099 | CAAGGTGGGTGGATC[A/T]CCTGAGGTCAGGAGT | 23607 |
rs557635635 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47574660 | TGGATTTAGAAAATA[C/T]TAAATTACTTGATAT | 23607 |
rs557646620 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47585198 | GTCCCAGCTACTCAG[A/G]AGGCTGAGGCAGGAG | 23607 |
rs557687127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47519380 | ATGGTTTGGGTTTCT[A/G]GCTACTCTACTAGAG | 23607 |
rs557691314 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47564602 | TTGTGATTATGGGGT[A/G]GAAAGTCAGTGGTTG | 23607 |
rs557726365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47529853 | AGAGCTTTATATCAG[C/T]CGTCTGCTCGCCTTG | 23607 |
rs557729902 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47487804 | CATATCACTTATTTT[A/T]TTGTATTTACAAAAT | 23607 |
rs557732781 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47534582 | TGGAGGAACTTGCCT[G/T]TAATTCCAGCTACTT | 23607 |
rs557735922 | snp | C/G | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476135 | CTTAGCCCATCACCA[C/G]CCTCATTCTTCCAAA | 23607 |
rs557761307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47563354 | GTTTGCCACTACATT[C/T]TGCTTAATATGCAAA | 23607 |
rs557767612 | snp | A/G | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625821 | CAACTTACATTAGGG[A/G]TTTGGGGGAATGCTA | 23607 |
rs557770509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47577748 | TGCCCCCCACCCCCA[A/G]CCTTTTTTAAGTAGA | 23607 |
rs557782413 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47578457 | GCGTCAGGCAATCTT[C/T]CCACATCAGCCTCTG | 23607 |
rs557799813 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47526934 | TATGAAAAATACTTA[G/T]TGCAGTCTGAAAACT | 23607 |
rs557823579 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47512350 | CTGTCTCAAAAAAAA[A/C]AAACATAAAAAGGTG | 23607 |
rs557854112 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47589043 | ATCATAAGGAATGCA[A/G]TTTAGGTTCTACTTT | 23607 |
rs557869786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47535248 | ATTCAAAAAACTGCA[A/G]CCTCTGGCATAAATG | 23607 |
rs557872061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47527795 | CAGTGGCCCTGCCCT[A/G]GATTTCATTATTTTT | 23607 |
rs557896290 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47506855 | GGAGAGGGAGAGAGC[A/G]GCTGTGGCAGTTTCT | 23607 |
rs557912236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47564038 | AGTGGAGAAGGAATC[A/G]TACCAACTAGATGTA | 23607 |
rs557927770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47498854 | TTTTTCCTGACTGAT[A/G]TCTTTCATCCAAGTA | 23607 |
rs557932409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47540717 | GCTAATGAGTAGTCC[A/G]TTTCACCTTAAGTCC | 23607 |
rs557945911 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47607842 | CTGAAAATCCATAAA[A/C]GTTATTTGCTTTATT | 23607 |
rs557963116 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47616925 | ATGATACTACATCCT[A/G]TTGTCTCTAACTTCT | 23607 |
rs557974020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47572099 | GTAATAACCAAACAT[A/G]TCTTCAGTTATTGCC | 23607 |
rs557993777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47497003 | CTCTCAATTCTTTTT[C/T]GGAATTATTATCCTT | 23607 |
rs558018124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47622744 | AGAGGGTCTGTCGGT[C/T]CTCTCGGGATTGCTG | 23607 |
rs558026011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47592513 | GTTCCTGGCACCATA[A/G]CTCCTAAAACCCTTG | 23607 |
rs558033092 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | CD2AP | GRCh38.p7 | 6:47500359 | GTCTACAGAGCAGTT[G/T]GGTATTTCATTTATA | 23607 |
rs558046847 | snp | A/C | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520867 | AGTGGGCTTTTCTTG[A/C]GTTTTGTTTTCTTCT | 23607 |
rs558052342 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47615356 | TTGCATTGCTATAAA[-/G]AAATACCTGAGACTG | 23607 |
rs558055612 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47488673 | AGGAGGATTGCTTGA[G/T]ACTAGTAGTTTGAGA | 23607 |
rs558062876 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47478941 | AGAAAAATACAAGGC[C/G]TTATATGTTATTTAC | 23607 |
rs558064284 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47526301 | CGGAGGAGTTCCAGA[A/G]AAGAAGGTGGTGGAC | 23607 |
rs558064620 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47497844 | AGCATACAGTTTTAC[A/T]GTTTGTGCCCCATGC | 23607 |
rs558067059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47489472 | TGAGCCACCGTGCCC[A/G]GCTGCACTCGACTAG | 23607 |
rs558073460 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47509989 | ATGATTTATCATGGA[A/C]CTCCATTTTGAAATA | 23607 |
rs558087336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47599927 | TTTTTTTAAGCTTTA[A/G]GACTGGTTTTTCAGC | 23607 |
rs558148048 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47587307 | TGTTCTGTCAGAGAT[G/T]TGGGGCGCAGAAAAG | 23607 |
rs558192234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47490171 | CAAAAACTGTAGACA[C/T]AGGGTCTTGCCATAT | 23607 |
rs558193969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47542017 | TTTCCTTGCTCTAGA[A/G]TATCTGCCACATCTG | 23607 |
rs558200488 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47539439 | CAGAAATAAGCAAGT[A/G]TATGGTATTTTTGAG | 23607 |
rs558211502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47531457 | CGAGGACTGGAGAGA[C/T]GATATGAGGGGAAAC | 23607 |
rs558231176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47622775 | GTTTGTTCTTGCAGT[C/T]GGTCTGGAGTTAAAA | 23607 |
rs558255870 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47482581 | GATGGGGTTTCACCG[C/T]GTTAGCCAGGATGGT | 23607 |
rs558274902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47538476 | GTCTCGAACTCCTGA[C/T]CTCAGGTGATCCACC | 23607 |
rs558291705 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47509422 | TGACACAGTGTTGCA[C/G]AGACCTTCAATTTGT | 23607 |
rs558332670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47494562 | TAGGCCTTTGTTACA[A/G]AGAATACTCAGGTTG | 23607 |
rs558355076 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47508872 | CAATAAGACTGTTTT[A/C]CTTTCTTATCATTGG | 23607 |
rs558372199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47557223 | GTAGATTCTGGATAT[C/T]AGCTCTTTGTCAGAT | 23607 |
rs558395331 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47543095 | GGTGGAGGTTGCAGC[A/G]AGCTGAGATTGCGCC | 23607 |
rs558414996 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47564584 | CATTCTAAATGTGGA[A/G]CTTTGTGATTATGGG | 23607 |
rs558419911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47593075 | CCCCAGAAAGACAGT[A/G]TCAGAATTGAATTAA | 23607 |
rs558449546 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47549803 | CACATTACCTGATTT[C/T]AAATTATACTATAAG | 23607 |
rs558497659 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47582458 | TCACTGCATGTGTTT[C/G]TCATAATGTAAACCT | 23607 |
rs558504866 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47585771 | TAACCATTGGAAAGC[A/C]ATAGGTGAAGCACTC | 23607 |
rs558512791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47486880 | AAAATTGAGACTACA[C/T]AGTCTTGGTTAGAGT | 23607 |
rs558513302 | snp | G/T | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521550 | GAGTGAGACTCCGTC[G/T]CAAAAAAGAAATGGC | 23607 |
rs558513422 | in-del | -/TG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47554850 | TATTTTTTGAAACTC[-/TG]TTCTTTCTTTTGAAC | 23607 |
rs558517397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47554902 | TCTACTTTAAAAAAG[C/T]AAATTATGATGGGGA | 23607 |
rs558533134 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47572187 | ACTGTAAAATTTAAC[A/G]TTCAACAACATCAAA | 23607 |
rs558539309 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47545945 | ATATGACAAAACAAG[G/T]TTCTTTACCATTCCC | 23607 |
rs558557913 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47589963 | GTGACCTGGGATTTT[A/T]ACTATCCCTACCTTA | 23607 |
rs558578035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47478386 | CTCCATTCTCCCCAC[C/T]GCCCCTTCTTGCCCT | 23607 |
rs558596382 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47524016 | AACAAATCTTTTAAA[A/T]GGAATTATTTGTACC | 23607 |
rs558603060 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47598571 | GGAATACTACTCAGC[C/T]GTAAAAAAGATGGAA | 23607 |
rs558618523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47591155 | CGAGAGCTACACACA[A/G]CAAAATGAATCTTAG | 23607 |
rs558633694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47598184 | CCAGGGAATACAAAT[C/T]AAAACCGCAATGTGA | 23607 |
rs558652595 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47514942 | CTGCAATCCCAGCTA[C/G]TCGGGAGGCTGAGGC | 23607 |
rs558664143 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626013 | TTTAATGACCAACCT[A/T]AGGTAAAACAAAAAT | 23607 |
rs558695872 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47583395 | AATAGCATTACTACT[C/G]TAAAAACCTTCTTTA | 23607 |
rs558698954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47605356 | ATTTCCTTTAGCAAG[A/G]CTTTCTGAATCATCT | 23607 |
rs558708217 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47552659 | CTCTGCCTCCTAAAC[A/C]TAACTCCTCAGTTGT | 23607 |
rs558716510 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47493766 | TTATAATTCTTTTTC[G/T]CTTTGCATTTCAGTT | 23607 |
rs558738835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47595752 | ATACAGAGAATGAAA[A/G]TTCATGTCTGCCTCT | 23607 |
rs558781576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47560654 | CTTATGTAATATTTG[A/G]AGGCACATGGTGTCC | 23607 |
rs558787067 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | CD2AP | GRCh38.p7 | 6:47562230 | ATATTATAATTCGTG[G/T]TTTATCAATAAACTA | 23607 |
rs558811172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47547653 | GAAACAGTGAATTTA[A/G]ACTATACCCTGGAAC | 23607 |
rs558845967 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47561599 | AATGCTTACATGCAC[A/G]TACAATCCCATACCT | 23607 |
rs558849547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47501132 | TGGCTCACGCCTGTG[A/G]TCCTAGCACTTTGGG | 23607 |
rs558925968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47481971 | TCCCTGTCTTGCCCA[A/G]GCTAGTCTCAAACTC | 23607 |
rs558956120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47503780 | TTCTCATTTGAGCCT[A/G]CAGTATACTTGTGAA | 23607 |
rs558962217 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47503785 | ATTTGAGCCTACAGT[A/G]TACTTGTGAAATAGT | 23607 |
rs558962870 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47586018 | GGCGTCCATTGTCTG[A/T]TTAAAGATTGCCAGG | 23607 |
rs558974715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47548150 | CTCAAGAAACGAGAA[A/G]AAGAAGAACAAACCA | 23607 |
rs559017269 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47511027 | GCAATGAGCTGAGAT[C/T]GCGCCACTGCACCCC | 23607 |
rs559019046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47502969 | GGAAGTGGGGATCAT[A/G]GAGACCACCTCAGAG | 23607 |
rs559047057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47586046 | AGGCATAGAAAGAGC[A/G]AGAAAATAGCAATAC | 23607 |
rs559060192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47489614 | TTTAGGGAATTCTTA[C/T]TATGCTAGGCTGAAT | 23607 |
rs559060228 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47526305 | GGAGTTCCAGAGAAG[A/G]AGGTGGTGGACCTCA | 23607 |
rs559077112 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47550039 | TGGATCCTCATCTCT[C/T]ACCTTATACAAAAAT | 23607 |
rs559087656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47490799 | GATATGTGCTAAGAG[C/T]GTATTGTACTATGCA | 23607 |
rs559107616 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CD2AP | GRCh38.p7 | 6:47564326 | AAGCATATGAGTGAA[A/G]TGATCTTTGTGATGC | 23607 |
rs559107820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47600654 | TTTATTCGGTATGTT[C/T]TATATGGTGAAAATT | 23607 |
rs559170846 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47563587 | GAGGGGCACCAAACA[G/T]TTGTGTACAGTATTA | 23607 |
rs559170917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47571227 | CTGGTTATTGGAGGT[A/G]TATATTAAAACTATA | 23607 |
rs559182575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47604638 | TCACCCTTCAAATTA[C/T]GACATATTTTAACAT | 23607 |
rs559198143 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47560361 | TAATCTCCATACACC[-/T]TTTTTTTTATTATTC | 23607 |
rs559216713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47619719 | CTGATCACCTCATCC[A/G]TGCCAACATCTACTG | 23607 |
rs559218069 | in-del | -/T | 0.210301 | 0.246828 | intron-variant | CD2AP | GRCh38.p7 | 6:47488026 | TAATGGATGAGATCC[-/T]TTTTTTTTTTTTTTT | 23607 |
rs559234087 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47505000 | GAAGGCTGGGGTGGC[A/T]GTGGCAGTTTCTTTT | 23607 |
rs559246737 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47605580 | TGTCTAAACAAAGGT[A/G]CAGTGAACTATAAAC | 23607 |
rs559273632 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47507705 | CCGCCTTGGCCTCAG[A/G]AAATGCAGAGATTAC | 23607 |
rs559274053 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47612717 | CATTTGCAACAACAT[A/G]GATGGAACTGGAGGT | 23607 |
rs559284263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47510332 | GATACCTCAGTAGCC[A/G]TGAGTACATCCAGTG | 23607 |
rs559287599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47606492 | AATCAGAAGGAAATT[A/G]TCATGAGGCTATAGC | 23607 |
rs559325478 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47552428 | TGAGTTACTTCACTT[A/G]GAATAATAGCCTCCA | 23607 |
rs559383090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47542459 | TTAATTTCCATTGTG[A/G]TGATATTAATAGGTA | 23607 |
rs559410469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47508227 | ATAGAAGGTTTCATC[C/T]CCATTGAAAATCTGT | 23607 |
rs559422478 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47543075 | AGAATCGCTTGAACT[C/T]GGGAGGTGGAGGTTG | 23607 |
rs559504702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47622818 | GTCTCCGCATGCTGT[C/T]CTGTCTGGAGCCGCA | 23607 |
rs559542166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47551660 | GTGGCAAAGAATAAC[A/G]GTTGTATTATGCCTG | 23607 |
rs559575052 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47501085 | TAAAACCTTCCCAGA[A/G]GAAAGAATTCATTCA | 23607 |
rs559576240 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47616865 | GCCTGCAACAGATCA[C/T]ATTTTTTACCATTGC | 23607 |
rs559582510 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47482800 | TATTTATTCATAATT[C/G]AGATCTGTCAGAGAA | 23607 |
rs559594497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47614917 | AATTCTCCACTGGTG[A/G]TTGGCAATTTCGACT | 23607 |
rs559600312 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47512143 | AGCCTGGGCAACAGA[A/G]CGAGACTCCGTCTGA | 23607 |
rs559633432 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47609432 | CTGTAATCCCAGCAC[A/T]TTGGGAGACCAAGTT | 23607 |
rs559642907 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47607255 | TGTATTCTTGTGAAT[A/C]GTGCTACAGTAAACA | 23607 |
rs559701036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47608964 | TGTATTCTTTAGTTG[C/T]CTGGTGATTTTTCCA | 23607 |
rs559730545 | in-del | -/A | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47597837 | ATGGCTGTCTGGAAT[-/A]AAGTTGGCCTGGGTG | 23607 |
rs559747012 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47614861 | TGGTGACATATGGCT[A/G]TAGATTCACTGCCTC | 23607 |
rs559760479 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47558598 | GCAGTTTTTGTCATT[G/T]ATTCTGTTTATGTGA | 23607 |
rs559766079 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47508080 | TCTCAGAATGGTGAA[C/T]ATGCAATGACTTCCA | 23607 |
rs559766270 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47535199 | TTATTACTATCCTGC[C/T]GTTCAAGGTCATTGC | 23607 |
rs559770347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47547208 | ACATGTCAATACTAA[C/T]GTTGAGTGTAAATGG | 23607 |
rs559778237 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47505504 | TCTATTCCACAAAGC[C/T]GCCATTGTCATCCTG | 23607 |
rs559811408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47550906 | ATGAGATTGGAGACT[A/G]TTATTTTAAGTGAAG | 23607 |
rs559835465 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47565753 | TATTTTCTTTTTACC[A/C]CCTTCACTGCCGCTA | 23607 |
rs559863809 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47510599 | TAGTATTTGATTTTT[A/C]TGTAAAATACAGCAT | 23607 |
rs559871577 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47572303 | CAAGTGCTGGGTGAC[A/G]AATTGTTCTGTATCT | 23607 |
rs559876743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47561866 | GCTCACTGCAACCTC[C/T]GCCTCCCGGGTTCAC | 23607 |
rs559899298 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47612419 | GCCTGTAAACATTAG[A/T]CAAATAAATTATTTA | 23607 |
rs559932679 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47579542 | GAACATTTTGCCACT[A/T]TTCTTTTGCAAACAA | 23607 |
rs559934783 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47551161 | GTAACCTAACACCAC[C/T]GGTTCCCCAATAACC | 23607 |
rs559962976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47500893 | GCTGGGACTACAGGC[A/G]CCTGCCACCACGCCT | 23607 |
rs559972072 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47620040 | CTCTGTTGACTGTTC[A/C]ATTTGCCATGCAAAA | 23607 |
rs559978848 | snp | A/G | 0.000527504 | 0.0162319 | missense | CD2AP | GRCh38.p7 | 6:47503337 | ATGAATTAACTATTC[A/G]AGTTGGAGAAATCAT | 23607 |
rs559992030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47516761 | ATGAAAAGTTAGAAA[A/G]CAGGACAGTGGAGGC | 23607 |
rs560006896 | snp | A/G | 1.64912e-05 | 0.00287147 | missense | CD2AP | GRCh38.p7 | 6:47554653 | TTTTTCAGGTAGAAG[A/G]AGGCTGGTGGAGTGG | 23607 |
rs560031677 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520667 | CCTTATTATAGCCTG[A/T]TGAGGATGGAAGTCT | 23607 |
rs560035003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47604783 | TTATTATGGTTTGTT[A/G]TATTTCATGATTATT | 23607 |
rs560060391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47619345 | TTTCCATTCCTGAGT[C/T]ACTTCATTAGAATAA | 23607 |
rs560099566 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47565300 | CTTTGCTAGGAAAGT[A/G]TTATGTTTCGGTTTT | 23607 |
rs560101530 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47522584 | ACCTTGATATAAAGT[G/T]TTCTAGACTTTTTGA | 23607 |
rs560125133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47582852 | CAGTGGCGCAATATC[A/G]GCTCACTGCAAGCTC | 23607 |
rs560147787 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47555346 | TGCTGTTGGAATTAG[G/T]AGAGTTTTTTTTGTT | 23607 |
rs560175801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47605758 | TGAAGTTCAAAACAA[A/G]TTTTACATGCTGATT | 23607 |
rs560210964 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47528769 | AAGGATGTCTCACCT[A/G]TCTTTTTTTGTGCCG | 23607 |
rs560213076 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47478549 | CTCTGCTAACCCCTT[A/G]CCCAGCTAAAATCAG | 23607 |
rs560214735 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47596312 | CATTTTTAAAGAATG[C/T]GGTACATCACATTAA | 23607 |
rs560231565 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47590409 | ATATCTGAACTGAAA[C/T]ATAAGGAGACAAAAA | 23607 |
rs560236304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47568725 | CTCCAGCCTGGGTGA[C/T]AGAGTGAGACTCCGT | 23607 |
rs560272220 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47597514 | GCTAGAGCACCAGGA[C/T]ACTTGAGCAGGAGAT | 23607 |
rs560281330 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47592742 | GGGTTTGTGAACACA[C/T]TGAGGGGATAGGAAG | 23607 |
rs560288748 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47525934 | GAGTTTGCTTTGACT[A/G]TACATGATTGCTTTC | 23607 |
rs560325110 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47608187 | TAGCTTCATCAGACT[A/G]TTTTCTGCAAATGTT | 23607 |
rs560350680 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CD2AP | GRCh38.p7 | 6:47569555 | CAACTAGATGGATGC[A/G]TCACACAAAACATTT | 23607 |
rs560352249 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47614043 | AGAGAGTTAGGGCCT[A/C]ACTCTGGATTAGGCT | 23607 |
rs560362272 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47575650 | TGTTCAGATTTTTAA[A/T]TAATGACATCTAAGG | 23607 |
rs560365016 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47611904 | TATTGAATATTCACT[G/T]AAAGCTATAGAAAAA | 23607 |
rs560388374 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47612302 | AATTTTTAACTGTTA[C/T]ATTGAACCATTCTAA | 23607 |
rs560394270 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47621356 | ACATTTATTGACTTG[C/T]GTATGTTAAACCATC | 23607 |
rs560395845 | in-del | -/TTCCTTGACAGTATT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47588184 | AGCTTAAAATTTTGC[-/TTCCTTGACAGTATT]TTCCTTACCTACACT | 23607 |
rs560430577 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47531750 | ACTAGCACATTATCA[C/G]TTCTCAAGTATTTGA | 23607 |
rs560519332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47573531 | TCTTGCCCTGTCGCC[C/T]AGGCTGGAGTGCAGT | 23607 |
rs560525894 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47533391 | TTCCTTTATCTTCAT[A/C]TCCAGTTCTGATAAA | 23607 |
rs560536645 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47488870 | CACTCCAGCCTGTGC[A/T]ACTGAGTGAGTCTTT | 23607 |
rs560542580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47533354 | TTGGGGTGAGTGGTC[A/G]GGGTGGGGTTTGAGC | 23607 |
rs560562410 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47572570 | GCCACCTGTAAAATG[A/G]TCATTTCGATAGATG | 23607 |
rs560591013 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47532610 | TATTTTGTTTCATTT[A/G]TCAGTACTGTCTTTA | 23607 |
rs560598993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47495782 | GAAACTGCCAGTTGA[A/G]TATTTTAAAAATTTG | 23607 |
rs560613166 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47621804 | GAAATTCATCCATCT[C/T]TTCTAGGTTTTCTAG | 23607 |
rs560688807 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47598337 | CACTATGGAAAGCAG[A/T]GTGGAGATTCCTTAA | 23607 |
rs560691295 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47581029 | CATTTTTAGAAATAT[A/G]TGAAAATTGAGTGTT | 23607 |
rs560717635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47536378 | CCAAAACCATTGTAT[C/T]AACATAAGGTTAATA | 23607 |
rs560740862 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47543587 | GTAGAGGACCACTGT[C/G]TCCTTGTTTTCTCAC | 23607 |
rs560753092 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47619743 | TCTACTGTTTTTTGA[G/T]TTTTTGATTATGGCC | 23607 |
rs560761138 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47503875 | TTTTGTCCACTGTTG[G/T]TTAGCTAAGACAAGA | 23607 |
rs560848289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47623483 | AGTGTGGAACATTGG[C/T]ATCCTGTTTAATGTC | 23607 |
rs560854353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47529524 | GATAGGCTCTGGCCA[C/T]TGGAAACCCTGAACT | 23607 |
rs560879653 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47496345 | AGTCTGAATGTTGCT[G/T]CTTTGATAACCTTTG | 23607 |
rs560930115 | in-del | -/AGG | 0.00795532 | 0.062565 | utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47478190 | CGCGCGAGCCACCAC[-/AGG]TGGAGGAGGAGGAGG | 23607 |
rs560936943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47528946 | TCTCCCATTATGTGG[C/T]TTATCTTCTCACTCT | 23607 |
rs560946363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47507604 | GCTCCCACCACCACG[C/T]CCAGCTAATTGTTTG | 23607 |
rs560947675 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47485663 | GGCCTTCACATTTGC[C/T]CACCACTCACTGACT | 23607 |
rs560949705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47494957 | TTGAGCCAAGGAGTT[C/T]GAGACAAGTCTGGGC | 23607 |
rs560966029 | snp | A/G/T | 3.3252e-05 | 0.00407739 | missense | CD2AP | GRCh38.p7 | 6:47595861 | TATTTTAAATCTTAG[A/G/T]TGAAAAATCAACACT | 23607 |
rs560968022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47603674 | TTTATTCATTCTACA[A/G]CTGTTCTTTTTTCCT | 23607 |
rs560968783 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47558534 | TTTTTAGCATGAAGC[A/G]GTGTTGAATTTTATC | 23607 |
rs560971655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47580279 | AATTTGTAAAAACCA[A/G]GTCCACCAACTTAGA | 23607 |
rs560994045 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47617865 | ACTTGCTGATTCTCC[A/T]TTGTGCCTCTTACAA | 23607 |
rs560994984 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47494003 | TTAGCATATTAATCA[C/T]AGTTATTTTAAATTT | 23607 |
rs560995902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47484422 | GATGTTCTACACTCT[C/T]CCTGACCATTTTCAC | 23607 |
rs560999260 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47597947 | CCCAGTGGTGTCTCT[C/T]CTTACCACATGCAGC | 23607 |
rs561001697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521565 | TCAAAAAAGAAATGG[C/T]ACAGTAATAGCTGTT | 23607 |
rs561008202 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624335 | TTGTTGTGATAAATA[C/T]GAGCAAATGAAGTGT | 23607 |
rs561051296 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47485037 | GATGCTGGTGTCAAC[A/C]AACCCGCACTACCAG | 23607 |
rs561068271 | snp | A/G | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520163 | GGGGCTAAATTGACT[A/G]TGGAAAGTTATTTCA | 23607 |
rs561068905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47499795 | TCGCAGTGGCACGAC[C/T]TCGGCTCACTGCAAC | 23607 |
rs561086231 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | CD2AP | GRCh38.p7 | 6:47614830 | TTCTTTCTTTGCTCA[C/G]GGACAGGACTGGTAG | 23607 |
rs561088832 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47601560 | CATGCTAAGATAAAA[C/G]GCATAATTGATGGAA | 23607 |
rs561088893 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47567662 | TTGAGATCCCAAAAT[A/G]GCTAGGAAATTTCTA | 23607 |
rs561113827 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47482503 | CCTGCCTCAGCTTCC[C/T]GAGTAGCTGGGACTA | 23607 |
rs561127232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47567316 | AAAATCTGAAATTTA[A/G]AAGTCAAAGCCGGCA | 23607 |
rs561192513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47566764 | ATGATGGCTTCCAGC[A/G]TCATCCATGTCCCTG | 23607 |
rs561201853 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | CD2AP | GRCh38.p7 | 6:47549676 | GAATTCCTATACATA[A/C]CACCATCATTCTTCA | 23607 |
rs561202316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47501429 | CTGATTGTACTTAGT[A/G]TCTGAGAAGTACATA | 23607 |
rs561205888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47491161 | AAGAATAAATATTTC[A/G]TTCTGGGAATAATTT | 23607 |
rs561229854 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47603246 | TATTTATGTATGAAA[G/T]ATTTTAAAGATAGTA | 23607 |
rs561235374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47587709 | TTTTGGAATGCAAGT[A/G]GGGAGGCATGTAAAT | 23607 |
rs561259082 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47545692 | ATGGTTCACATCACG[C/G]GACTCTGTGCAGACA | 23607 |
rs561290900 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47602708 | TAGCCTGGGTAACAT[A/G]GTGAGACCGTGTCTC | 23607 |
rs561296443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47502207 | TAGGTTGGCTTACAG[C/T]ATAGCAGCTTGTGTC | 23607 |
rs561300941 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47495595 | TAATAAATAGATCTC[A/G]TCCGTGACTCTCTGG | 23607 |
rs561349507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47489009 | GATTCTTACTGCTGC[C/T]GTTCTTACAAGTTCT | 23607 |
rs561371728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47599206 | CAGAAAGTAATCGGT[A/G]TTAGGCCATACAATC | 23607 |
rs561395509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47537453 | CTGTTCTAACTTTCT[A/G]TTTTATTTGGAAAAT | 23607 |
rs561397488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47546266 | AAATAACTTCAGAGC[C/T]TAAAGACAAGGTTTT | 23607 |
rs561409470 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47509021 | TCACTAAACTTGGTC[A/T]TTTCTAGCTTTTGAT | 23607 |
rs561440440 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47587640 | TCTTTCAGTAAGATA[A/C]TCATCATGTCATTGG | 23607 |
rs561450623 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47585531 | GTCTAGAAGCAGTTT[A/G]CAGGCAGCAGAAAGG | 23607 |
rs561471030 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47610348 | GAAATGAGAGTGAGG[G/T]TGCTCATCCCTTGTC | 23607 |
rs561479456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47514944 | GCAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 23607 |
rs561514195 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47570213 | CTCCAAACAAGTAAT[A/T]GCATTTTGCAGTTCT | 23607 |
rs561539242 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47609500 | TGGACGACATGACAA[A/T]ACCCCATCTTTGCAA | 23607 |
rs561556852 | in-del | -/ATCA | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47560197 | CCCATTTGCTAACTT[-/ATCA]TTCACCTTCTATCTA | 23607 |
rs561583614 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47623973 | GCTGAAAGGGCTATA[A/G]TTGCTTTTTTCTTAT | 23607 |
rs561615873 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47515457 | TTGCATATTCACATA[C/T]GTTATCTCACTTTAT | 23607 |
rs561627624 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47608524 | TTTAAGAAGGTCATT[C/T]AGGTTTCCTCCCAAA | 23607 |
rs561643453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47551974 | TGCCCTTTACAAACT[A/G]GCATCTGTTGGTTAC | 23607 |
rs561651141 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47541388 | CTCGGCCTCCCAAAG[G/T]GCTGGGATTACAGGC | 23607 |
rs561675126 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47508556 | TTTTTGTTTTTTTTT[G/T]TTTTTTTGGGACGGA | 23607 |
rs561711160 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47556395 | GAACTCATTCTTTTT[C/T]TTTTTAATTTTGTTT | 23607 |
rs561753048 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47526473 | AAGATTTTTTAAGTT[G/T]CTTTCCCCCTTTTAT | 23607 |
rs561757770 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520620 | GGTGGTGGTTGGGGG[C/T]GAAAGTGGGGTCTAT | 23607 |
rs561802343 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47550239 | AAAGAGCTTTTGTAT[G/T]GCAAAAGAAACAGTC | 23607 |
rs561820238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47592560 | AAAGGTGAGAGGAAC[A/G]TCTTTTGTTATTTAT | 23607 |
rs561829742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47514067 | TTCTAGTTAATTTCT[A/G]GTAGTTCTTAATGTA | 23607 |
rs561871620 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47517958 | TCAGCATTTTACATA[A/C]ATAAGATGGATAGGA | 23607 |
rs561879995 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47511580 | TTAACATTAGGCAAA[A/C]CTGAATTAAGAGTGT | 23607 |
rs561895340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47513583 | TGTTTAAGACTGCAC[A/G]TACAGTATTATAGGA | 23607 |
rs561948563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47512714 | CTTAAGTGTTACTTT[C/T]TAATAAAGAGAACAT | 23607 |
rs561969975 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47555520 | AGGTATTAGGAGTAG[A/C]TCATAACCTTAAGGT | 23607 |
rs562007022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47518898 | CCCAGGTAGCCTCTG[C/T]TGTGGTATTTTTTAG | 23607 |
rs562018939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47519999 | TGTTAGGATTTGAGT[A/G]TAAGTTCTAACTTCT | 23607 |
rs562026401 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47608826 | TTATAATGCTGTTAC[A/C]TTCTTGCCCCTGTTT | 23607 |
rs562080201 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47527275 | GAAGTATACCTGTTG[A/T]TGCTGCTCTTGGTCT | 23607 |
rs562086120 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47622337 | AGATTTGCCGCCCTA[A/C]CCAGAGTTGTGGCCT | 23607 |
rs562095083 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47565241 | TTTCTATATAAAAGT[C/T]CAAGATAAATTTCTT | 23607 |
rs562102047 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47480030 | GACATTGGAATACCT[A/G]TTTTGATTGTCCAGA | 23607 |
rs562109622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47572263 | AGTGACTCATGCCTG[C/T]GCCCGGATCCACTGC | 23607 |
rs562134599 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47482703 | TAATTGAGGGATTTG[A/C]AAACTAAAATGACAT | 23607 |
rs562152280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47524125 | TGTTAATGTTTGCCT[C/T]GGACTTAATCTGGAA | 23607 |
rs562188875 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47479680 | TAAAGTTAATTACAC[A/T]GTTCTTTTCTGTCTT | 23607 |
rs562235555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47578979 | ATCTTTCTCTTTTTT[C/T]CTCTGAGAACATTTT | 23607 |
rs562243135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47488366 | ACATATACTTTGAGA[C/T]ATACTGAGTTGTTAC | 23607 |
rs562254983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47608179 | GAGTTGTTTAGCTTC[A/G]TCAGACTATTTTCTG | 23607 |
rs562261723 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47528638 | TAGGCAGTGGAAATA[C/G]AATAAAACATAATCC | 23607 |
rs562303293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47534112 | GAATTTTGATAGTGC[C/T]TTTTCTTCAGTTGTT | 23607 |
rs562315119 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47504558 | CTCTAGGTTAACTTA[G/T]AATACCTAGTAAAGT | 23607 |
rs562340206 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47585888 | CAGTGTATCACCTTA[C/G]ACTAAAGGTTTCTCT | 23607 |
rs562350159 | in-del | -/TTTTTTTTTTT | 0.00716266 | 0.059414 | intron-variant | CD2AP | GRCh38.p7 | 6:47616083 | CCACTGCGCCTGGCC[-/TTTTTTTTTTT]TTTTTTTTTTTTTTT | 23607 |
rs562358836 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47619263 | CAAAGTCTGTTCTAT[C/T]ATTCTTATGCCTTTG | 23607 |
rs562375736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47571555 | GAATTTTGTGTTGCT[A/G]AACACCTGAAGTGAG | 23607 |
rs562411288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47493999 | ACCCTTAGCATATTA[A/G]TCATAGTTATTTTAA | 23607 |
rs562424687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47509802 | AGTGGTATTTTGGCG[A/G]ACTACAGTAAGATGG | 23607 |
rs562433955 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47481845 | GTTCAGTGGCATGAT[C/T]ATAGCTCACTGCAGC | 23607 |
rs562447169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47561155 | GGAGGTACAATTTAC[A/G]TACAGTAATTGTGTC | 23607 |
rs562463395 | in-del | -/CTTTT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47508398 | TCTGCTAGCTTCAAA[-/CTTTT]CTTCTGCAACTTCCT | 23607 |
rs562490390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47516566 | TCATGATGTGCAATG[A/G]ATGCTTTGTTTACTT | 23607 |
rs562499841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47575365 | TATATTGAATAACTT[C/T]AGTTGATTAATGATT | 23607 |
rs562513874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47576418 | ATTACTATCCTAGCT[A/G]TAAGTACCATTAGGG | 23607 |
rs562535085 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47567591 | TAAATGTATATAAGT[A/G]GGCTAATCCAGACTT | 23607 |
rs562538073 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47477991 | GGGTAGGGCCCTCCC[A/G]CCGCCGTGGCTCCTG | 23607 |
rs562556956 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47604091 | TTCTCTCCAAATTGG[A/T]TATTTCATTTTGCTT | 23607 |
rs562561678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47478476 | TCGCTCTCCCTTCTC[C/T]GCCTCTTTTCCTGTT | 23607 |
rs562597916 | snp | A/G | 0.000443173 | 0.0148792 | intron-variant | CD2AP | GRCh38.p7 | 6:47612438 | ATAAATTATTTAATC[A/G]AAAGACTTAACAGTA | 23607 |
rs562620740 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47537590 | ACATATACTTTTTTA[A/G]TGGAATCAGTTGAAA | 23607 |
rs562754840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47618444 | CTTTGAGACTGTAAG[A/G]TTGTTTGGGTAGGAT | 23607 |
rs562764667 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47564970 | TTCTCCTCCTCCTCC[C/T]TTTCCCTTTTTCCTC | 23607 |
rs562775646 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47599144 | TTTATTTTATTGTGA[A/T]CAGCCTTAGGAGAGA | 23607 |
rs562795698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47621076 | CTAGGACTTCCAGTA[C/T]TATGTTGAAGAGGAG | 23607 |
rs562798021 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47542469 | TTGTGGTGATATTAA[C/T]AGGTAGGATCTTTTT | 23607 |
rs562840607 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625257 | TTTCCTATTTTGACA[A/G]GTTAACTTGTAAATA | 23607 |
rs562849638 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47627590 | CTTTCATTTGTATTA[C/T]ATTGTTCAAAGGGGA | 23607 |
rs562862620 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47547187 | TGATGAATGGAATGG[C/T]GTCTCACATGTCAAT | 23607 |
rs562882579 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47515821 | AAAAATCAAACTGTT[C/T]CTCAAATTGCAATTT | 23607 |
rs562899803 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47539810 | GCTTTACTTATATAA[C/T]GATTTTTAGAAGACA | 23607 |
rs562900542 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CD2AP | GRCh38.p7 | 6:47587565 | TCCCAGAATGGTAAT[A/G]ATATTACCACTTTGA | 23607 |
rs562900586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47579692 | CCTTTGTTTCTTTCT[C/T]GACTGTACTGAAAAA | 23607 |
rs562901280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47597398 | ATGTTAGAAAAGCCA[A/G]GAAGCAGACAGCATA | 23607 |
rs562925275 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47543846 | GGGTGGAGCTTGAGA[C/T]ACTACATATCTCACA | 23607 |
rs562962096 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47586933 | CATAACAAAGGAAAT[G/T]ATTCTAAGTATTTTC | 23607 |
rs563008276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47525151 | AATCATTTCTAGACT[A/G]TTTTTTAAAATGTAA | 23607 |
rs563032010 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47487941 | AACAATACAAAATTT[A/G]AATATATTGAAATAT | 23607 |
rs563120186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47596773 | TCCTTTGGATATGGA[C/T]CCAGTAATGGAATTG | 23607 |
rs563129437 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47557502 | TGAGTTAATTTTTGT[A/G]TAAGGTATAAGGAAG | 23607 |
rs563135258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47544035 | TGAGAACACAAGCGC[A/G]AATGGTTATAAATGA | 23607 |
rs563138765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47561795 | ATTTATTTATGTATT[C/T]ATTGAGACGGAGTCT | 23607 |
rs563151592 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47594320 | TACATAAATATGTTG[A/C]CATCTTATAGTAGTT | 23607 |
rs563161781 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47505729 | GGCTGAGGGGCTCCT[C/T]ACTTCCCAGTAGGGG | 23607 |
rs563169770 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47607847 | AATCCATAAAAGTTA[C/T]TTGCTTTATTATCCA | 23607 |
rs563232922 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47613148 | CCACTGAAGTCTTCA[A/G]TCCTCAAAGTCATCC | 23607 |
rs563267154 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47550081 | GGATCAAGGACTTAA[A/G]TCTAAGACCTGAAAC | 23607 |
rs563304809 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47581195 | TATTGACCTGGCCAA[A/C]TAGTTATTCTACCGT | 23607 |
rs563343797 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47528867 | GTTTGCTTTTTTATT[G/T]TTGACTTTTAATATT | 23607 |
rs563347282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47623460 | TGACAAGTCCTGTGT[C/T]ACTTGTTAGTGTGGA | 23607 |
rs563351095 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47502311 | GTCTTTTTCATTATC[-/T]TTTTTTTTTTTTATT | 23607 |
rs563353143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47513471 | TGGTCTGCAAACTCT[A/G]TTTTTTATATAGTCA | 23607 |
rs563375537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47565089 | TAATATATGGACAAT[A/G]TTGAGTCTTCACAGA | 23607 |
rs563392217 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47604548 | TAATCTCTACAGGCT[A/G]AAATGATTGGATTGT | 23607 |
rs563405239 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47528006 | TAATAGAAACATGTT[G/T]TATATATGTGGTGTT | 23607 |
rs563447708 | in-del | -/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47582790 | TTTTTGTTTTTTTTT[-/G]TTTTGTTTTTTTTTT | 23607 |
rs563475658 | snp | G/T | 1.6834e-05 | 0.00290116 | intron-variant | CD2AP | GRCh38.p7 | 6:47608051 | GCATTGTGGTCTAAG[G/T]TTTGTTGACTTTCTG | 23607 |
rs563479144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47602965 | AGCATTCATTGTTGA[A/G]TAAGGAAACACATTT | 23607 |
rs563485276 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47500790 | CCTGCCCTGTCACCC[A/G]GGCTGGTGTGCAGTG | 23607 |
rs563490087 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47506608 | GGCTGGAGACCGGCC[C/T]GGCCAACACAGCGAA | 23607 |
rs563551544 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47508411 | AACTTTTCTTCTGCA[A/T]CTTCCTGACCTCTCT | 23607 |
rs563559138 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47543511 | ACAGTTTTGGACGAT[G/T]AGAAGTCCAAGATCA | 23607 |
rs563575526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47593618 | CCACTTCACACCCAC[C/T]GAGATGGTTAAAAAT | 23607 |
rs563592454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47545620 | ACCCCGCCCGCTGGT[C/T]CCAACCACCACTTCC | 23607 |
rs563601117 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47522961 | ATTTAGAAAAAAATT[A/C]TTTTTTTAGAAGGAT | 23607 |
rs563603123 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47609479 | TCCAGGAGTTCGAGA[C/G]CAGCCTGGACGACAT | 23607 |
rs563622101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47507734 | ACAGGTGTGAGCCAC[C/T]GTGCCTGGCCAAAAT | 23607 |
rs563637209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47600772 | TTTGATCAGTTCATA[C/T]TGTTTTCTGTTTGAT | 23607 |
rs563658012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47551874 | GTTGACTCTCTTACA[A/G]TGTAGGCATCTCAAG | 23607 |
rs563694528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47573920 | AAATTGCATCTTGCT[C/T]TTCTGGATATTTCAG | 23607 |
rs563712607 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47512215 | GGAGTGGTGACATGC[A/G/T]CCTGTAGTCCCAGCC | 23607 |
rs563712769 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47525392 | CAGAATTATTACTGT[A/G]TTTAGGAATTTGGTG | 23607 |
rs563713219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47558991 | CTATTAATTACTGCC[C/T]CAATTTCAAAACTTG | 23607 |
rs563716910 | snp | A/G | 5.09152e-05 | 0.0050453 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624267 | TGTTCCAGGGATTCA[A/G]AAGCAACGCTATGAA | 23607 |
rs563756504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47511386 | AGAAACTGACATTGA[C/T]CAGAAGAGGCAAAGG | 23607 |
rs563765195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47536596 | TTTTTTGGGATAGTA[A/G]TGAAGCCGTGAAAAC | 23607 |
rs563795592 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47552712 | AGGTAATAGACAGCT[G/T]ATGTTTCTCTCCGTT | 23607 |
rs563798824 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47529334 | TGTCTGTGGAGTTTG[C/T]ATATTCTCATGTTTG | 23607 |
rs563819257 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47561472 | CCTATCAAGGCAAAC[-/T]TTTTTTTTTTTTTAA | 23607 |
rs563829095 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47545177 | CAGGACTAGACTGCA[A/G]CTCCCACTGGGATAG | 23607 |
rs563829641 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47504728 | CACCACAATAGAGCA[A/C]ATGTCATAGTAGAGC | 23607 |
rs563830042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47566712 | GAGTGAGAACATGCA[A/G]TGTTTGGTTTTCTGT | 23607 |
rs563844935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47595218 | TAAAATTGTCAAAAT[C/T]GTTTTTTTCCAGCTT | 23607 |
rs563851787 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47555944 | AGTGTCTTACATATG[A/G]AAGAGTAAAAATTTT | 23607 |
rs563860103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47558827 | TGGTATCAGGATGAT[A/G]CTGGCATCATAAAAT | 23607 |
rs563871703 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47565845 | CTGAATAGTCTGGTA[A/G]CCAGTAGTGATCACC | 23607 |
rs563877034 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47617690 | CTTGTTCTGATGCTT[A/T]CTATCTTCTGCTTAG | 23607 |
rs563880384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521506 | GCAGTGAGCCGAAAT[C/T]GCACCAGTGCACTCC | 23607 |
rs563881014 | in-del | -/GA | 0.00914312 | 0.0669923 | intron-variant | CD2AP | GRCh38.p7 | 6:47489814 | ATTATATCTTAAAAC[-/GA]ATTTTGAGAAGGAAG | 23607 |
rs563924362 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47620129 | TTTGTTCATGAAATC[C/T]TTGCCTGTGCCAATA | 23607 |
rs563927808 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47605893 | CACCAAGTACTTTTT[G/T]TTGAGATCTAGGTCT | 23607 |
rs563935824 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47496458 | AGGGAATTTAACCCT[A/G]TTTACCATATGGCAT | 23607 |
rs563936783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47573314 | ACAGATTATGAACTA[C/T]TGACCTTTTTAAAAT | 23607 |
rs563980481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47558682 | GAAGCTGACTTGATT[A/G]TGGTGGATAAGCTTT | 23607 |
rs563993327 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47548987 | TGCAGAAAAAACATT[-/A]AGACAAAATCCAGCA | 23607 |
rs564000194 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47479459 | TCTAATTTTATGTTC[C/T]CTTCTCCACCTCCCT | 23607 |
rs564004470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47613131 | ATCTTCAGTTCTTTT[C/T]TCCACTGAAGTCTTC | 23607 |
rs564013018 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47522002 | CCTGGGCAACAAGAG[C/T]GAAACTCTGCCTCAA | 23607 |
rs564018591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47510671 | TAAATAAACGGGAGA[A/G]AGGATAAATTGAAAC | 23607 |
rs564058221 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47555421 | GAATATGTTTTTCTC[G/T]ATGGAAATGTATATG | 23607 |
rs564065920 | snp | A/G | 1.75339e-05 | 0.00296085 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47612515 | TTTGGAAGAAGAGAA[A/G]ACAATGAGAAGTAAT | 23607 |
rs564109027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47562934 | ACCCTATAAAGAAAT[C/T]GGTTGTGGTTGGGTA | 23607 |
rs564143588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47527171 | TTTTGAACAGTTACA[C/T]GAAGAGGTCATGTTC | 23607 |
rs564145874 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47591468 | ATGTTAGGAAAATAG[G/T]TTCAATTAAGAATAG | 23607 |
rs564150409 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47501864 | GAGGTAAAATAAATA[C/T]ATATTAATCTTCATT | 23607 |
rs564160565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47548761 | ACAAAAAAAGAAAAC[C/T]ACAGACCAATATTCC | 23607 |
rs564219369 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47614041 | GAAGAGAGTTAGGGC[C/T]TCACTCTGGATTAGG | 23607 |
rs564259195 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47595330 | CTAAGAATTACAAAT[A/G]TAAGCCTATAATTCT | 23607 |
rs564267481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47517350 | TGCAGTGGTGCGGTG[C/T]GATCACAGCTCGCTG | 23607 |
rs564387158 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47601766 | GCCTTTTTAATATGT[G/T]TTAGAAAGTTGAAAA | 23607 |
rs564418369 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47611882 | TAAAATTTGTGAAAA[A/G]ACATAATATTGAATA | 23607 |
rs564422952 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47592312 | CTCAAAAGAATGAAG[C/T]TGGAGCCCTACCCCA | 23607 |
rs564435014 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47620784 | TAGGTGTATTCCTAA[A/G]TATTTTATTTTATTT | 23607 |
rs564452837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47620901 | GTAGCTCTTATACCC[A/G]AAACTTCGCTGAATT | 23607 |
rs564471317 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47571387 | CCTGAGAAAAGGGGA[A/G]AGAACAAGGGGAAAG | 23607 |
rs564491961 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47622330 | GCAAACCAGATTTGC[C/G]GCCCTACCCAGAGTT | 23607 |
rs564533527 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47481727 | GATTTCTTTATGTTA[C/G]TTTGTTGTACTGTTT | 23607 |
rs564535531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47615904 | CCCACCTCGGTCTCC[A/G]GAGTAGCTAGGACTA | 23607 |
rs564541772 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47596158 | TTTTAAAATTGACAT[A/G]TACAATTGTGTGTAT | 23607 |
rs564564456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47556372 | ATTCATGACCCTCCA[A/G]AGGACATGAACTCAT | 23607 |
rs564605641 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47564533 | TCTGTTAGAAATACC[C/G]TTCCTTCTTTGTTTA | 23607 |
rs564613078 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47578183 | GAAGAAACTTAGAAG[G/T]TCTTGTTAATTAAAA | 23607 |
rs564643906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47519703 | GCTCAAGAACTGCCC[A/G]TTCATATCTGAAAGG | 23607 |
rs564656259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47517880 | TGTTATGAGTATCCA[A/G]TGAGATGATGTATTA | 23607 |
rs564668815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47481189 | CATTTCTAGAGCACA[A/G]AAAAGGAATATTTGT | 23607 |
rs564689879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47574890 | TACAGTCTGTAGAAC[A/G]TTTTTTCACAGTTCC | 23607 |
rs564708650 | snp | A/T | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476168 | GTAAATGGCCTTCCT[A/T]ATGGGCTGCTTGAGC | 23607 |
rs564712167 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625212 | AATAGGAAAACAAAA[C/T]CCAAAGCTTTTCAGA | 23607 |
rs564720500 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47478518 | TGCGGGATGGGGGGC[-/G]GGGGCGCCTGGCCAC | 23607 |
rs564755973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47581713 | ACATGTTGGATACTG[A/G]AAAAATAGAATGTTT | 23607 |
rs564758550 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47585677 | CAGCGAGTACTCAGA[C/T]CTGTAGACAGCTTAC | 23607 |
rs564773617 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47497325 | CCTTTCCTTTCCTTT[A/C]CTTTCCTTTCCCTTC | 23607 |
rs564805237 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47515694 | GGGGCAAGTGATATA[A/C]ATCCTAGTCATTGAA | 23607 |
rs564806549 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47529576 | ATCTTACTGGTTTTT[A/G]TTAATTTTACTAAAT | 23607 |
rs564835938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47488928 | TTTTGTTTTTTGTAC[A/G]TGTTTATTTTGGGTG | 23607 |
rs564840684 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47504312 | CCAGCTTGGACAGTA[G/T]TTGTTAGCAGAATAC | 23607 |
rs564861656 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47536429 | ATGTTCAGTTTAAAT[C/T]CCTGTGTGCCAAGAC | 23607 |
rs564888269 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47583004 | TAGCCAGGATGGTCT[A/C]GATTTGCTGACCTCG | 23607 |
rs564890690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47590342 | CATATATAAGTATAT[A/G]TAAATATATACACAC | 23607 |
rs564908283 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47480046 | TTTTGATTGTCCAGA[A/G]GCTTTTTCTTTGTGA | 23607 |
rs564923108 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47573997 | TATAGAATGTAGACA[G/T]TATGACAGGATGTCA | 23607 |
rs564932079 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47619200 | ATACTGCACCACGTT[C/T]GTAGTCTTTCATCCC | 23607 |
rs564934095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47485365 | AGGCTAATGTGTGTT[C/T]GTGTCTTATAAGAAA | 23607 |
rs564953417 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47548010 | CTTTCAAAACCTCTG[A/G]GATAGCAAAGGCAGT | 23607 |
rs564953925 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CD2AP | GRCh38.p7 | 6:47526487 | TGCTTTCCCCCTTTT[A/G]TTTGTATCTTTTGTC | 23607 |
rs564955347 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47589639 | ATGAAGAATCATAAG[A/C]TCAAGATAGAGGGGA | 23607 |
rs564960822 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47482355 | CCTGTAGAAATGAGC[C/T]GGAAGTTTGCTTTGT | 23607 |
rs564977012 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47519437 | ATTGTGACAGGAGTA[C/T]GGCCTTTGGAATCAG | 23607 |
rs564996054 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47477967 | GGGAAAACCGCGGTC[A/G]GGCGGGCGGGGTAGG | 23607 |
rs565009842 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47583272 | CATTGACACTTCTTT[A/G]TCACTCAAAGTCCAT | 23607 |
rs565018970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47618261 | GGAGGCAGAGGTTGC[C/T]GTGAGCCGATATCAT | 23607 |
rs565057961 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47538511 | TCGGCCTCCCAAAGT[C/G]CTGGGATTACAGGCA | 23607 |
rs565069013 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47512836 | CATAGTTTTACACCT[A/T]TTTGCCTGTGCATAA | 23607 |
rs565070043 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47493034 | CTCTTGTCCCTTAAG[A/G]CATTGATTAATTTCA | 23607 |
rs565091541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47595124 | GAGCACCTGAAAGAT[C/T]AGGAAGCAGGTATGT | 23607 |
rs565121462 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47496163 | TTCTTTTTGTGTAGC[A/G]AAGTCCCACTTCTGG | 23607 |
rs565136744 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47537972 | GCAAGGCTGGTCTCA[A/G]ACTCCTGGCCTCAAG | 23607 |
rs565188848 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47560278 | CCAAGAATAAAGTTA[G/T]TCTCTTATGTAACTA | 23607 |
rs565201562 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47535842 | CTGTCCATAGTAAAA[A/T]CCATTTACAACTTTC | 23607 |
rs565206797 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47627471 | AAGCATTTTACAGTG[A/G]TGGATATGATAAAAA | 23607 |
rs565208634 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47495004 | GTCTCTACAAAAAAA[A/T]TTCAAAAAATTAGCC | 23607 |
rs565260902 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47488889 | GAGTGAGTCTTTCTT[-/A]AAAAAAAAATTAATA | 23607 |
rs565269931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47486570 | TGATGATATACTGAG[C/T]ACTGGCAGTAGTTAA | 23607 |
rs565270494 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47538125 | TTCATGTAATGAATA[A/T]TTCATTACATGAAAA | 23607 |
rs565279315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47487254 | AAATTTTCAGAATGC[A/G]TGTCAAATGGAAATA | 23607 |
rs565301414 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47593098 | TGAATTAAATTATAG[C/G]ACACTCAGCTGGTGC | 23607 |
rs565337048 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47587122 | ATAAATCAAAGTTCT[A/G]CCCTTGTTCCCATAG | 23607 |
rs565340801 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47598233 | GAATGGCCATAAATC[-/A]AAAAAATCAAAAAAT | 23607 |
rs565392634 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47508143 | GAGAGTGAGCCTGTC[C/G]TTTGAAGCCTTGAAG | 23607 |
rs565405969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47531044 | CACTTGAGCCCAGGA[A/G]TTGAAGACCAGCCTG | 23607 |
rs565409572 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47480730 | ATTCTTGTACCAACT[C/T]GGGAAAAAAAAAATC | 23607 |
rs565411621 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47489092 | CAGGTAGTGAGTTAT[A/C]TCGATTGCTTAGTCA | 23607 |
rs565413332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47495571 | GGCTCCAGCAGCTTC[C/T]ACTCTAGGTAATAAA | 23607 |
rs565450394 | in-del | -/A | 0.004257 | 0.0459388 | intron-variant | CD2AP | GRCh38.p7 | 6:47599475 | AGCGGTGGTGCATTT[-/A]AAAAAAAAAATTGTC | 23607 |
rs565452182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47552833 | TTCATGCTTTACTGC[C/T]TTCCCTTTCTCCCCC | 23607 |
rs565480065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47603301 | TATTTTAAAGTAATA[C/T]TTAACATATTTTTCT | 23607 |
rs565482675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47611527 | TATCACTAAGAAATT[A/G]TTGCCAAGAAGTTAG | 23607 |
rs565511048 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47575990 | GATAGTTATGAGGCT[A/G]CTAGTCCTATTTGCA | 23607 |
rs565525237 | in-del | -/AA | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47623327 | TGATGCCATCAGGAT[-/AA]GGCAAGGCCTATATA | 23607 |
rs565555924 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47497478 | TGCTCATTGCAGCCT[C/T]CACCTTCTGGACTCA | 23607 |
rs565569613 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47600901 | ATATTTTAAATTTTC[A/G]CAAATTTGGGGGATC | 23607 |
rs565617175 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47592051 | TTGTTGCCCAGGCTT[G/T]TCATGAACTCCTGGC | 23607 |
rs565624419 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47501617 | TGGTCATACTCACTT[G/T]CCTTTTTTTTTTTGG | 23607 |
rs565667264 | snp | A/G | 0.000182039 | 0.00953869 | missense | CD2AP | GRCh38.p7 | 6:47533689 | AGTCTTGTACAACGA[A/G]TAAGCACCTATGGAC | 23607 |
rs565678648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47591674 | CATCTGAATTAATAA[A/G]TGGGTTAACTTATTA | 23607 |
rs565685066 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47585418 | AACAACTGGAAAATT[A/G]GACAAAATGTATGAA | 23607 |
rs565715053 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47542888 | GGGCATGGTAGCTCA[C/T]GCCTGTAATCCTAGC | 23607 |
rs565773676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47547569 | AATGAGATAGTAAGA[C/T]AATAATAGTGGGGGA | 23607 |
rs565779225 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47517490 | GAGGTGGGGTTTGCC[A/G]TGTTGCCCAGGCTGG | 23607 |
rs565781323 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47547031 | CTAAAAGGAGCTCTA[A/G]ATCTTGAAGCAAATC | 23607 |
rs565798514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47526714 | GGTCAGATTGGAGTT[A/G]CTTTCAAGAGGAACA | 23607 |
rs565833353 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47578621 | TCATATTCTCCCTCT[C/T]CACCTTCCTCTCTTT | 23607 |
rs565845688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47548144 | GGGCACCTCAAGAAA[C/T]GAGAAAAAGAAGAAC | 23607 |
rs565851385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47543620 | GGTCTTTCCTTTGTA[C/T]TGGAGGGTTGGGGAG | 23607 |
rs565881681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47504228 | TTTCTTACATCCAGC[C/T]TCATTCCCTGGCCTC | 23607 |
rs565906040 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47555567 | TTTTGTTTTTAGAAC[C/T]GGCTTAATGCAAATA | 23607 |
rs565911046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47550303 | TCTTCACAATCTATA[C/T]ATCTGACAAAGGACT | 23607 |
rs565932525 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47541567 | TTTATCTACTTGATG[G/T]TTATCTCTGTTTTGT | 23607 |
rs565936798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47512311 | CGCACCACTGCACTC[C/T]AGCCTGGGTTGCAGA | 23607 |
rs565950209 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47491309 | TGTGTGTGTGTAATA[G/T]ATATAAAATCAGGAA | 23607 |
rs565956528 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47552743 | TGTTGTATTTATTCT[A/T]GTTTGGTCTACATCT | 23607 |
rs566010233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47621536 | TTTTCTGGTTTTGGT[A/G]TCAGGGTGATGCTGG | 23607 |
rs566029654 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47555285 | AGAGTATGATTGACA[A/C]AATTTTACCCCAAAG | 23607 |
rs566044922 | in-del | -/ACAA | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47546963 | TACAGTCTTTTTCAG[-/ACAA]ACAAATGCTGAGAGA | 23607 |
rs566070169 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47512902 | AATTGTTTCACATTG[C/T]ACCTTTTCTTTATAT | 23607 |
rs566085248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47593005 | TTGAGATTGGAATCT[A/G]AAGTGGGAGCAGTCT | 23607 |
rs566104998 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47549733 | TTCATATGGAACCAA[A/G]AAGAGCCTGCATAGC | 23607 |
rs566141896 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47585069 | GAGGCCGAGGTGGGC[A/G]GATCATGAGGTCAGG | 23607 |
rs566142993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47509932 | CAAAACATTTATATA[A/G]TTCTCTTGAGTGTAT | 23607 |
rs566143395 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520129 | TTGGAATGGAAAAAA[C/G]GTAGTTCATTTTAGG | 23607 |
rs566150127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47498718 | TTCTTATTTTATAGC[A/G]TTCTGTTCTTTTAGA | 23607 |
rs566154571 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47612777 | AACTGCATGTTCCCA[C/T]TTATTTGTGGGAGCT | 23607 |
rs566154768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47587185 | GGACCAATTTGAAGC[A/G]TCTTAAGCCTTCCAC | 23607 |
rs566185876 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47538407 | CCACCATGCCTGGCT[A/G]CCTTTTGTATTTTTA | 23607 |
rs566205934 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47533295 | TTTGTTTACCCCTGA[C/G]TTTGAATTATTGTTT | 23607 |
rs566220250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47593825 | AGAATTGACAACAGA[C/T]TCTCGTGTATTGTAT | 23607 |
rs566247098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47546674 | AAATATAGGAAGTTC[A/G]AAGGACACCTGGGAA | 23607 |
rs566253738 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47502172 | GACCTCCTTAAGTTG[C/T]TTGCTTGTGGCCCTC | 23607 |
rs566312987 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47618585 | CTTAAATTCGCAGCA[A/T]GTAATGTAGAAATTG | 23607 |
rs566330651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47600414 | CCTTATTATAAAATA[C/T]GCTATTACATTTCAG | 23607 |
rs566331333 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47515187 | GACTACTTTGGCTGA[A/G]TGAAAGTTTTCATAT | 23607 |
rs566358005 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47501839 | ATAATCTAAAATCCT[G/T]TTATTAAAAGAGGTA | 23607 |
rs566363227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47557110 | ATAGGTTTGTTGGCC[A/G]CATAAATGTCGTCTT | 23607 |
rs566365719 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47499148 | GGCTAATCTTATACT[C/T]TTCCTGCTTAGCCTT | 23607 |
rs566387800 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47490440 | TGAAACATGCTTAAA[A/C]ATAATTTCTAGTGTT | 23607 |
rs566391980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47607712 | ACCTAAATGGAGAAA[A/G]TCCTTACTGCTAAGA | 23607 |
rs566406485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47509385 | CCCATGCCGTTGGAA[A/G]AATGGCATTGATGGG | 23607 |
rs566442692 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47553956 | TAGGAAGTTATGTTT[A/C]TTTTCTTTTTTCTTT | 23607 |
rs566458171 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47563617 | ATGCTCTACCATATA[G/T]TCGTTGTGGATTACC | 23607 |
rs566470850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47604205 | TGTCGTGCCTGTTAT[A/G]CCACGTGTACAGTGT | 23607 |
rs566501591 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47569590 | AACCCTGATGGATTG[A/T]TCTTCAAGAGTTCTA | 23607 |
rs566503620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47562131 | CTAAACATCGCAAGC[C/T]ACAATTGTGTTGCCT | 23607 |
rs566524350 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47603328 | TTCTTCTTTGATACC[A/G]CAGAATTAAAATTGC | 23607 |
rs566556981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47589877 | GGAGGAAGTATGAAA[C/T]GGAAATAGACCTAAC | 23607 |
rs566595639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47598071 | AGAAAGAAACAATCC[C/T]ATCAGAAACTGGACT | 23607 |
rs566611643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47502603 | GGTTCAAGCTATTCT[C/T]CTACCTCAGCCTCCC | 23607 |
rs566612866 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47589429 | ATATATACACAAATA[G/T]ACACACATACACACA | 23607 |
rs566617167 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47596936 | TATTATCTTTTATCT[C/T]TTTGAAAAGTTAAAG | 23607 |
rs566623153 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47603469 | TCTTAAAGCACCAAG[C/T]CATCCTTTTGGAAAC | 23607 |
rs566634749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47563050 | TGTATCACATTTAAA[A/G]ATTTAGTTTGAGGAA | 23607 |
rs566652031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47609900 | TACTAGGAAAAATAT[C/T]GTATTTTGGATCTGG | 23607 |
rs566660893 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47479703 | CTGTCTTAAATGGGA[-/T]TGCAGAATAAAATTA | 23607 |
rs566663708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47560580 | TTGTCTTTTTCCCCC[A/G]ATTCCTCATGATTAG | 23607 |
rs566716863 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47539218 | GTAAGTGCTTGATAA[A/C]TGTTTACAGTTATTC | 23607 |
rs566721596 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47478078 | TGAAGAGACTGGTAG[A/G]AGAGCGCCGCGGGCG | 23607 |
rs566744779 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47612690 | AGTCACAAAAAAAGA[A/T]TGAGATCCTGTCATT | 23607 |
rs566818426 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47495665 | GCTCTGTGTCCTCAA[-/T]TTTCTAATGGGTCCA | 23607 |
rs566853138 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47554834 | CTAGTGTTTTATTTT[G/T]TATTTTTTGAAACTC | 23607 |
rs566854646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47621235 | GTATGCCAGTTTTGC[C/T]GAGAGTTTTAATCAT | 23607 |
rs566873087 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47517495 | GGGGTTTGCCATGTT[G/T]CCCAGGCTGGTCTTG | 23607 |
rs566881040 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47605189 | TAGACCAAAGGAATC[G/T]GCTATTAGTTAGAAC | 23607 |
rs566924895 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47605985 | AAGAGGATTTTTTTT[G/T]TTCTTTTAAGGGCGA | 23607 |
rs566946371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47511735 | TTGGCTTTATCACTT[C/T]AGATGTGTATGTTAA | 23607 |
rs566956128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47572430 | TTGAATGTTAAAAAT[A/G]TATTACAAAACTGTC | 23607 |
rs566973986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47583299 | CCATAGTTTCCTTTA[A/G]TGTTCACTCCTAGTG | 23607 |
rs566984694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47613263 | ATGAATTTTTTCCAA[A/G]TGGTTTTCAGTTTAT | 23607 |
rs566994103 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47601237 | CATAGCTGTTATTTA[C/T]TCCCTATATAGTAAA | 23607 |
rs567006508 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47575026 | ATACTATTAAGTTTC[C/T]TCCTAAGATAGGTGG | 23607 |
rs567011636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47510877 | CAAGAGATCGAGACC[A/G]TCCTGGCCAACATGG | 23607 |
rs567015282 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47584011 | AATTCCGTAATGATA[C/T]ATGATGTTGAATATC | 23607 |
rs567065074 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626614 | ACCACTAAGCTTCTG[C/T]CTTAATACAAAGCTG | 23607 |
rs567077569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47524633 | TTCCACTGTACTTCA[C/T]TTGGCTCTCATTTAC | 23607 |
rs567081448 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47600063 | ATTAAAGGCATTGTG[C/T]CTTCATTACTTTCTG | 23607 |
rs567085196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47579274 | CAGGAGGTTGAGGCT[A/G]CAGTGAGTCATGATC | 23607 |
rs567118218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47539837 | GACAATTTTTGTACA[A/G]TTAATTTTTTTGTAG | 23607 |
rs567133740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47517052 | TCTGGCATGAATGAT[C/T]TAGCGCCATGCCCTT | 23607 |
rs567140079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47620443 | CATGCTGTTTTGGTG[A/G]CTGTGGCCTTATAGT | 23607 |
rs567146224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47486707 | TTATCCTTCTTACTG[C/T]CCTATCAGTGTTCCA | 23607 |
rs567149813 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CD2AP | GRCh38.p7 | 6:47585219 | GAGGCAGGAGAATGG[C/T]GTGAACTCGGGAGGC | 23607 |
rs567169860 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47581010 | CAAGTATGATGTCTG[C/T]AAACATTTTTAGAAA | 23607 |
rs567179908 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47619588 | GGTAGATACCCAGTA[C/G]TGGGATTGCTGGATC | 23607 |
rs567179966 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47627718 | AGAATGAAATTTTTA[A/G]AATTGGAAACAAAAA | 23607 |
rs567210269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47487438 | GCTCACGCCTGTAAT[C/T]CCAGCACTTTGGGAG | 23607 |
rs567210606 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47478920 | TAGACTTCCTTGCCG[G/T]AGGAGAGAAAAATAC | 23607 |
rs567218113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47579747 | AATTTAAGAAGGGCT[A/G]TCTATCCTAATAACA | 23607 |
rs567230041 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47570656 | AAAGTTTTAAAAAAA[G/T]AATAGACACTGAGCC | 23607 |
rs567266913 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47524855 | TTCAAAGTAGGTCTG[C/T]TATATCTGTCATTTT | 23607 |
rs567293626 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47602604 | TAAAAGGCAATTTCA[C/T]GCCTGTGATCACAGC | 23607 |
rs567329801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47507397 | TCTAGAAACCTTTCC[A/G]GGAGGTTTTCAATTT | 23607 |
rs567344632 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47514340 | ATACCTCATTAATTT[G/T]TTATGTTTAAGAAGT | 23607 |
rs567350082 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47482889 | ACTTTAATGTATATA[A/T]AAAATTGTAATTGTG | 23607 |
rs567350764 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47599861 | CTTAATCTAGAGATA[C/T]TTTTATTTCCAGTGG | 23607 |
rs567358569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47557926 | TTGGGCAGTATGGCC[A/G]TTTTCATGATATTGA | 23607 |
rs567387159 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47608581 | TTTTTGTCAGCGTTT[C/G]CAATTTATTAAATAC | 23607 |
rs567392375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47618046 | TTTAGTGGCCGGGCA[C/T]GGTGGCTCACACCTG | 23607 |
rs567398769 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47484179 | GACAGTAGCTCACAG[C/T]AGAGACATTTATTAT | 23607 |
rs567405978 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47513875 | GATACCATCAGACTT[A/T]AAAAAAAATTTTTTT | 23607 |
rs567409002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47528119 | TTTTATCAGATGCAT[A/G]TACTGTAGTTTATTT | 23607 |
rs567422637 | snp | A/G | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624393 | TGAATTTATATATAT[A/G]TTTTGTTTTGCCAAT | 23607 |
rs567428935 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624824 | GGTGATGAAATAGGA[G/T]TTTCCTAGCTATATA | 23607 |
rs567446348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47534510 | TCAGGAGTTCGAGAC[C/T]AGCCTGACCAACATA | 23607 |
rs567457995 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47484885 | GAGCCCCTTAGGAAT[C/G]TTTTGGTCAATAATA | 23607 |
rs567476751 | in-del | -/TAA | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47488443 | ATGTGAAATTAATTT[-/TAA]TAATATTTTGAATGT | 23607 |
rs567519122 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47530713 | GTTAACATTTGTATG[C/T]CTAGCTGCTGCCTGG | 23607 |
rs567527466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47480128 | ATGTTGGTATACTCT[C/T]GACTACTTAGAATGT | 23607 |
rs567531431 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520291 | ATATTTATAACAGTC[A/T]ATATTGGTTGAGGAC | 23607 |
rs567532855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47492464 | TTCAAGTGATCCTCC[C/T]CCGTTAGGCTCCCAA | 23607 |
rs567532998 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47581186 | AACTTAATATATTGA[C/G]CTGGCCAACTAGTTA | 23607 |
rs567543755 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47489882 | GACTCTCCTAGTGTG[A/G]TTTAAAAAATAAAGA | 23607 |
rs567553431 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47483231 | TCAGTCTTTCTAGAT[A/G]GGGGAGGCGACAGAA | 23607 |
rs567554169 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47477522 | TGATCCATCTGAGGC[A/G]ACAAACCAGACCAAA | 23607 |
rs567573675 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47622621 | CAGTTTCTCCAGTGC[A/G]GGGTGTGTGTTCGGG | 23607 |
rs567578819 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47527687 | GTAACTATGTTGTCA[C/G]CTGTGCCAGGAAGCT | 23607 |
rs567589229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47482356 | CTGTAGAAATGAGCC[A/G]GAAGTTTGCTTTGTT | 23607 |
rs567589455 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47478255 | CCAGCATGGGTAAGA[A/G]ACTCGGGCGCTTCCC | 23607 |
rs567600985 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47595361 | CTCGTCTGTGGCTAA[C/G]CAGTCTTGCCCTAGT | 23607 |
rs567609986 | in-del | -/TAGTTTATA | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47547521 | AACACTGGAGCTCTT[-/TAGTTTATA]AGACAATTAGTAATA | 23607 |
rs567640519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47529282 | GTCGTTTTGTTGTAA[C/T]GTTGATGAAAAAAAA | 23607 |
rs567643433 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47560080 | ACTCCAGTACAGTGA[C/T]TTATTTTGAAACTTT | 23607 |
rs567681119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47529744 | AAAATCGGTTTCCTT[A/G]TACATTGTTTTGCTT | 23607 |
rs567774291 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47507899 | GATGCATCATCAATA[A/T]GCATTAGTATTTTCA | 23607 |
rs567776707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47526179 | TTGCTATTGAAATTG[A/G]TAGCCAAAGAGTAGT | 23607 |
rs567781225 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47616446 | ACCTTTGCACTTCGG[C/T]ACTAAATTATACTGT | 23607 |
rs567787227 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476993 | CTGCCCTGGAATTGG[G/T]TCTACTTAAACAGAA | 23607 |
rs567807698 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47623478 | TGTTAGTGTGGAACA[-/T]TTGGCATCCTGTTTA | 23607 |
rs567856442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47488481 | GGTTTAAAGAAAGTA[C/T]ATTATTTCATAATGT | 23607 |
rs567914625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47545259 | GCAGGAATATGTTAG[A/G]AAAGCCGAGAGAACC | 23607 |
rs567922024 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47604980 | TTTTTTCTGCCTTAC[C/G]TTTGTGTCCTCCATC | 23607 |
rs567977688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47544488 | AGCTGTTTAGAATGC[C/T]CATACGTTCTGTTTT | 23607 |
rs568000953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47598499 | AAGTATGGAACCAGC[C/T]CAGATGCCCATGAAT | 23607 |
rs568005736 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47584891 | ATTGCTGGCTTTATT[A/G]TCTATTTTTTTACTA | 23607 |
rs568021510 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47579084 | AATACGTGGGAAATA[C/T]TTTCTTTTAGGACAG | 23607 |
rs568030731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47621400 | TATGAAACCCACTTG[A/G]TCATGGTGGATTATC | 23607 |
rs568031551 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47540333 | CATTTATTGACTTTG[C/T]GCAGTTTGAAATGTG | 23607 |
rs568094179 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47549121 | GGGAAAAATTGAAAG[A/C]ATTCCCTCTGAGAAC | 23607 |
rs568155827 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47491521 | AGAAGGTTAATTTGA[C/T]AGACTCAGTTAGATG | 23607 |
rs568214136 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47549598 | ACATCTCATGGTCAC[A/G]GATGGGTAGAATCAG | 23607 |
rs568248301 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47618317 | GAACGAGACTGTCTC[-/A]AAAAAAAAACGAGTA | 23607 |
rs568304677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47554172 | TACCTTGGGCTCTCA[A/G]AGTGCTGGGATTACA | 23607 |
rs568314171 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47526603 | GAGCAATGAATTCAT[A/G]TATCATGTTAACATT | 23607 |
rs568371360 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47547464 | GTTAAAAGGCCTTGT[A/C]CAACAAGAAAGTATC | 23607 |
rs568389891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47503604 | ATGGATATCATTGTT[A/G]CTCTGTGTCCTGCTG | 23607 |
rs568448865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47519231 | AGGTGGAAAATGACA[C/T]TGATAAGTTGGGTGG | 23607 |
rs568470825 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47599671 | TTCTTACTGATCAGA[C/G]GACTGAAATAGATGT | 23607 |
rs568484184 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47591082 | ACAGCAAAAGAATGG[A/G]TAAAAGAGTTGAGGT | 23607 |
rs568484215 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47552172 | TATTTCAATAGGTGT[A/T]TGGGGAACAGGTGGT | 23607 |
rs568499350 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47559614 | TTAATAGATGATTCT[A/G]TTAAACATAATTGAT | 23607 |
rs568505867 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47592296 | CTCACAGCTGGATGT[C/T]CTCAAAAGAATGAAG | 23607 |
rs568523164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47592782 | CTGGAGAAGTTACGG[A/G]AACTCTGCATCTCTT | 23607 |
rs568532239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47563232 | GTATCACATCTCTAG[A/G]GGGAAGACAAATGTG | 23607 |
rs568543190 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47559514 | CAGTTGAAGCCTCCC[A/G]AAGTGCTGGGATTAC | 23607 |
rs568555077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47613657 | AATTCTTAAGGGCCA[A/G]GGATTTTCAGAATGA | 23607 |
rs568562708 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47588273 | TTAGATGTTTGTTTT[A/G]GGATATTCTTTACCC | 23607 |
rs568577353 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47586339 | GTTAGTGAACTTGAA[A/G]ACATAGCAAATAGAA | 23607 |
rs568642150 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47570782 | ATATAATGGAGGGGG[C/T]AAGATATGAATCAAG | 23607 |
rs568697010 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47511885 | ACAAAAAATTGGCCG[G/T]GGGTGGCTCACACTT | 23607 |
rs568701765 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47578252 | GTCGCCCAGGCTGGC[A/G]TGCAGTGGTGTGATC | 23607 |
rs568703843 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47569989 | TACTTTTTAGGAACT[A/G]TGCAATATTGATTGA | 23607 |
rs568741808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47606808 | ATGAATTTATCTTTT[A/G]TGTTACAAACCATCT | 23607 |
rs568752322 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47609988 | TGAGGTTGAGTTGGA[C/T]ATTTATAAAATGAAT | 23607 |
rs568765261 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47606767 | CATAATAATTATATC[-/AG]GGTAAATGCGGTATC | 23607 |
rs568768914 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47614247 | GCAAAAGGCCAATCT[C/T]TTGACCTGCTGTGGC | 23607 |
rs568769570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47508646 | TGCCTCCCAGGTTCA[A/G]GTGATTCTCCTGCCC | 23607 |
rs568791104 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47498578 | CTTTTCCTTATTTTC[A/G]TCTTTTTCTTTGTGC | 23607 |
rs568803558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47560430 | TGAAAAGGATTATAC[A/G]TGGAATTTATTTCCA | 23607 |
rs568841141 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47618476 | CATGTTTTTTTTTAT[C/G]TTTGCTCATAGCTCC | 23607 |
rs568880476 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47605350 | AAAGAAATTTCCTTT[A/G]GCAAGACTTTCTGAA | 23607 |
rs568887251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47501769 | GCAGGAAAGCTGTTA[C/T]TGCTTTTTAAAAATT | 23607 |
rs568890340 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47599964 | ATATCTTTGTCTAAT[A/C]TGTACTTCCTGTTTT | 23607 |
rs568934751 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624534 | TTTTTTATTGAAACT[C/T]GTATTATTTTTAAAG | 23607 |
rs568939851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47545351 | AGTCACAGCAAGATC[C/T]ACCCAAGGAGAGTCT | 23607 |
rs568982859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47595697 | ATTATTAAATTAAAA[C/T]ATAACTTTAAAATAA | 23607 |
rs569011374 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47617388 | GATTAGCTCTAGTGC[A/C]TCTCCCCTCTAAATC | 23607 |
rs569067540 | snp | C/T | 3.36355e-05 | 0.00410081 | intron-variant | CD2AP | GRCh38.p7 | 6:47582104 | AAAAAGCAATTATTT[C/T]TTTTATTGTCATTTT | 23607 |
rs569088520 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47581198 | TGACCTGGCCAACTA[C/G]TTATTCTACCGTTTC | 23607 |
rs569097439 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47617991 | GCTCAAACAATTACC[G/T]TCATTAAATTGATAC | 23607 |
rs569128118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47568457 | TATAAGAAACGATGA[A/G]TAGGCTGGGCGCGGT | 23607 |
rs569139532 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476614 | GCTGCTGTTTGTGAG[G/T]TTGATCATTCTTGTT | 23607 |
rs569204980 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47575177 | TCTGGCATTAGGATT[G/T]TGGGGTCAAATTGAT | 23607 |
rs569215032 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47593071 | CTAACCCCAGAAAGA[A/C]AGTGTCAGAATTGAA | 23607 |
rs569215676 | in-del | -/T | 0 | 0 | intron-variant | CD2AP | GRCh38.p7 | 6:47599283 | AGTGATTTTTGCGTG[-/T]TTTTTTTCTTATTTC | 23607 |
rs569273006 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47524499 | GACATTTTTTAGATG[A/G]ACAAAACTATTAGGA | 23607 |
rs569300388 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47478795 | AGTATTTGTTTTACT[C/T]GGGTTCTACCTAGGC | 23607 |
rs569317348 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47480324 | TTTGGTTTTACCAGC[C/T]ATCCTTTTTTCTTAT | 23607 |
rs569341421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47568941 | AAACCTATGAGAGTG[C/T]GGTAGTCAGTCAAGG | 23607 |
rs569348303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47517388 | GACTTTCTGGGCTCA[A/G]GCGATCCTCTCACCT | 23607 |
rs569353175 | in-del | -/CAGTAA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47538898 | GAAAAAGAACAAGGG[-/CAGTAA]CCTTACTGAGTCTGA | 23607 |
rs569423526 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47608951 | TAATGATTACAAATG[C/T]ATTCTTTAGTTGTCT | 23607 |
rs569440769 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47486617 | CTTCTGGCAAAGAGT[C/G]TTTAGAATGAAGTAA | 23607 |
rs569552119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47538303 | ACGGAGTACAGTGCC[A/G]TGATCTCGGCTCACT | 23607 |
rs569571081 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624828 | ATGAAATAGGAGTTT[C/T]CTAGCTATATAAACC | 23607 |
rs569594227 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47578482 | CCTCTGAAGTTACTG[C/G]GATTACAAAGCATGA | 23607 |
rs569610699 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47622451 | TGGCTGCCCTCCCTA[A/T]GGATCCCTGTGGTGC | 23607 |
rs569621994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520905 | TTGCATTGGCATTTC[C/T]ATGTTGCAGACTTCT | 23607 |
rs569687960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47622921 | TTTACAAGAAGTATT[A/G]CTGATTATGCATGCA | 23607 |
rs569703052 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47546882 | ATCTTGAGCCTCCTC[A/G]ACAAAACAATTATCA | 23607 |
rs569763610 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520263 | AGTCCTGGTAGAAGT[A/T]TCAGTGGTAAAAATA | 23607 |
rs569765824 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47544549 | ATGGCATGTAAATAT[A/G]CTGTTTTTAAAAATG | 23607 |
rs569767473 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47495183 | GAGAGAGAGAAATAG[C/T]CTTTTCAGGTGTGAT | 23607 |
rs569776732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47529270 | ATTTTGTTCAGTGTC[A/G]TTTTGTTGTAATGTT | 23607 |
rs569806477 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47599988 | CTGTTTTTTTTTTAA[C/T]ACCTATTATTATTTG | 23607 |
rs569818825 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47541612 | TTGGTTGCATGTAGT[G/T]TGCTTCTTTTGTTGT | 23607 |
rs569841110 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47481382 | ATGGAGTTTTGCTCT[A/G]TTGCCCAAGCTGGAG | 23607 |
rs569900276 | snp | C/T | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625284 | AATACTCAGGTTTTA[C/T]GATGTATAATTTACC | 23607 |
rs569922502 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CD2AP | GRCh38.p7 | 6:47506858 | GAGGGAGAGAGCGGC[C/T]GTGGCAGTTTCTAAG | 23607 |
rs569928318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47608503 | TCACTACAACTGAGA[C/T]ATAGATTTAAGAAGG | 23607 |
rs569932756 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47499329 | TGTGTGTGTGTGTTG[A/T]ATATATGTGTATCTG | 23607 |
rs569933120 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47544383 | GTGTAAATGGTGGGA[A/T]AAGATGTATAAAGAG | 23607 |
rs569955397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47484087 | TTTTTTTTGGTAATG[C/T]GTACCTGTCTTTGGC | 23607 |
rs569973834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47594610 | TTGTTATAACTACAA[A/G]TAGCTTTATTTCGTT | 23607 |
rs569979341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47489236 | GCAATGGCATGATCT[C/T]GGCTCACTGCAACCT | 23607 |
rs570000650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47601760 | AAACTAGCCTTTTTA[A/G]TATGTTTTAGAAAGT | 23607 |
rs570000808 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47587867 | GTGCTGAAGGCCAGT[C/G]TGGTTCTATACTTTC | 23607 |
rs570026082 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47587792 | GTAACTTTTATCTTA[C/T]GTCCTCCTCACTTCC | 23607 |
rs570059222 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47507324 | CTCCCATTAATGTTG[A/G]TATTTTTAGCTCCTC | 23607 |
rs570080386 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47514984 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 23607 |
rs570086458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47587313 | GTCAGAGATGTGGGG[C/T]GCAGAAAAGAGCTAC | 23607 |
rs570093247 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47492378 | TTTTTTTTGAGACAG[G/T]GTCTTGCTCTGTTTC | 23607 |
rs570101682 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47624095 | AAGTCTGAAGGCTTG[A/T]AAGTATGATCACATC | 23607 |
rs570110518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47551023 | ACAATGGACTTTGGG[A/G]CCTCGGGGGAAGAGG | 23607 |
rs570173564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47532005 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGACC | 23607 |
rs570233769 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47557782 | CAGCTTTGTTCTTTT[G/T]GCTTAGGATTGTCTT | 23607 |
rs570317844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47509458 | AAAAAAAAAATTCAG[C/T]TATTTGTGATGTGCA | 23607 |
rs570338998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47538537 | AGGCATAAGCCACTG[C/T]GCCTGGTGGAGAAAG | 23607 |
rs570349073 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47556791 | ATTAAACATATGTGT[A/G]TGTGTGTCTTTATAG | 23607 |
rs570375074 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47601165 | AATTTCAAACTATTG[A/G]TGATTGGAAAGTTCT | 23607 |
rs570393779 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47502727 | TCCATCTCTTGACCT[C/T]GTGATCTGCCTGCCT | 23607 |
rs570404741 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47499001 | ATATTCTTTTAATTT[C/T]ATTATTTTGATGCTC | 23607 |
rs570411341 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47554538 | TAAAGGGTTTATTTC[A/G]TAGTGCTAATTTTGT | 23607 |
rs570427773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47597842 | TGTCTGGAATAAAGT[C/T]GGCCTGGGTGATAAT | 23607 |
rs570435098 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47495349 | TTACGTAAGCAAAGG[A/G]ACACTAAAAATTGCT | 23607 |
rs570455946 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47510119 | AGAAAAGTTTAATCT[G/T]GGATTAAAAATTAAC | 23607 |
rs570478333 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47563619 | GCTCTACCATATATT[C/T]GTTGTGGATTACCTT | 23607 |
rs570498061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47486928 | AAAGTTGGTCTTTTA[A/G]ATGTATATACTATTC | 23607 |
rs570511925 | snp | A/G | 4.9476e-05 | 0.00497348 | missense | CD2AP | GRCh38.p7 | 6:47554677 | GGAGTGGAACCCTGA[A/G]TAACAAGTTGGGACT | 23607 |
rs570540992 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47563192 | TTCTGAGCGTATGTA[A/T]TCCCTATGTAGTCCA | 23607 |
rs570541604 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47496113 | TTAATCTTTTTCCTT[C/T]CCTTTGCTGTTCTCA | 23607 |
rs570549611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47539309 | ATGAAAAGGTAATTT[C/T]GTACTGGGGTTGTCA | 23607 |
rs570620699 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47597100 | CAGGGTGCTAAGCAC[G/T]ATTCTGTTGGCTGTG | 23607 |
rs570621628 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47556575 | GCTGGTCTTGAACCC[A/C]CGACCTCAGGTGATC | 23607 |
rs570629286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47516817 | GAGATGTAAATAGGA[A/G]AGTCATGGACAATCA | 23607 |
rs570680529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47604279 | ATATGTCATGAGTCC[A/G]AAATGTGCACTGTTC | 23607 |
rs570691666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47604951 | AAAATGCATATTACC[A/G]AACAGTGATGCCTTT | 23607 |
rs570707151 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47525398 | TATTACTGTGTTTAG[C/G]AATTTGGTGACTAGG | 23607 |
rs570709159 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47532749 | CTTTTGTTCTGTATA[A/C]ATTTAGAAACAGCTT | 23607 |
rs570832453 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47511827 | GACATTAAGGTGCAC[A/G]TTCATCCTGGCTAAC | 23607 |
rs570843984 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47526065 | TGCTATTTCCTGGCT[C/T]TTTTGGTAAAAGTGA | 23607 |
rs570847323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47614142 | ACAATAAGGCTGTTA[A/G]GTTTTCTTATTATTC | 23607 |
rs570864314 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47548248 | CAGAAAATACAAAAG[A/G]TAAATGAAACAAAAA | 23607 |
rs570869462 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47606049 | GTCAATTTGTGAGTT[C/G/T]TTCAAAGTAGTGGTA | 23607 |
rs570873904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47566895 | TTGGTTCCATGACTG[C/T]GATATTGTAAATAGT | 23607 |
rs570877322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47497009 | ATTCTTTTTCGGAAT[C/T]ATTATCCTTTATAAT | 23607 |
rs570904975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47598798 | ACTGCACATTGGGTA[C/T]AGTGTGCACTGCTCG | 23607 |
rs570910912 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47569155 | ACAACATATATTCAA[C/G]ATTTGTTTTGTTCTT | 23607 |
rs570933536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47620657 | ATGGTCATTTTCACA[A/G]TATTGATTCTACCCA | 23607 |
rs570934143 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47590522 | CCACGTATACACAGA[-/T]TTTTTTTCAGCCTAA | 23607 |
rs570938716 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47505174 | GGCAGAGGACCCTGC[A/G]GCCTTCCGCAGTGTT | 23607 |
rs570969295 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47560450 | ATTTATTTCCAGTGT[G/T]TCTTAAATCTGTAAT | 23607 |
rs570982044 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47599975 | TAATCTGTACTTCCT[-/G]TTTTTTTTTTAATAC | 23607 |
rs571091697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47517717 | GATCTTTTGATGGAT[A/G]TAGACAATCTGGTAT | 23607 |
rs571116285 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47569787 | TTAGTCTGCAGGCTA[A/G]TCACCAGGAGTCAAG | 23607 |
rs571163027 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47613142 | TTTTCTCCACTGAAG[C/T]CTTCAATCCTCAAAG | 23607 |
rs571187150 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47597228 | ACCTGTTTGTGCTGC[G/T]AGGCATCATGGAGAA | 23607 |
rs571219380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47602789 | ATGGTGTAGCTACTA[A/G]GGAGGGAGGCTGAGG | 23607 |
rs571237085 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47519050 | TCCTTGCGCTAGGAC[-/T]TTTTATAGGTGGCAA | 23607 |
rs571306279 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47580429 | AAACTAAGTCTATTT[G/T]TTGCTACTCTGTTTT | 23607 |
rs571332459 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47551328 | ATAGCACAGATTGAT[G/T]TTGTGTCAAAACACC | 23607 |
rs571346997 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47602124 | GATTTTCTTATTTAT[A/C]AAGTCATATGTAAAC | 23607 |
rs571368914 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47486893 | CATAGTCTTGGTTAG[A/C]GTGTTTTTGGGGGAC | 23607 |
rs571411610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47528261 | CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAG | 23607 |
rs571419637 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521678 | GCAAAAAGCTAATAA[A/T]CGTAGTTGATACCCT | 23607 |
rs571446182 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47500485 | ATGTTGGGATGTTTT[C/T]AGCTGTAAATAGAAA | 23607 |
rs571460630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47623790 | GTGAAAAACATGGAA[C/T]TAAACAGGTCTCTAT | 23607 |
rs571464973 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476488 | CTTGGTAGGGGACAA[C/G]GAACATAATGCTGAA | 23607 |
rs571466931 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47623032 | TTAATAACAGATCGG[G/T]CTGACAATGAAAGCT | 23607 |
rs571472054 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47509058 | CAGAGATGTGTGATT[C/T]TTCCTTTCACTTGAA | 23607 |
rs571480968 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47529060 | CTTCTTAGGTTGTAT[A/C]TACTGAATTATCTAG | 23607 |
rs571540834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47483075 | AAATAAAAACTAGTA[A/G]GATGTGATTGAAATT | 23607 |
rs571545228 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47543833 | GTAAGTAGATGTGGG[A/G]TGGAGCTTGAGATAC | 23607 |
rs571549257 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47512168 | GTCTGAAAAAAAAAA[A/T]ATATATAAAATAAAA | 23607 |
rs571602179 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47484047 | TAGTTATTAGAAAGA[A/C]CTTTTTTGTTGTTGC | 23607 |
rs571639828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47567837 | AAAAGTGTTAATCAA[A/G]TCACAGAGAAGCCAT | 23607 |
rs571659501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47530441 | GTTTGTATTTTCTAA[A/G]ATTTTTAATGTACCA | 23607 |
rs571680914 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47571586 | AACTATATGTAGAGA[A/G]CGCACCAGAACTGTT | 23607 |
rs571687586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47485797 | TTATGTTTAAATATA[C/T]AGATACTTAACCATT | 23607 |
rs571689217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47621255 | GTTTTAATCATAAAG[A/G]GATGCTGGATGTTGT | 23607 |
rs571701890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47575762 | GATTACAATGGAAAA[A/G]TGTCTAGTAGACTGT | 23607 |
rs571706315 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47621464 | ATTTTGTTAAGGATT[A/T]TAACATCTGTGTTCA | 23607 |
rs571713755 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47557043 | GAGATGGTAGCTCAT[C/T]GTGATTTTGATTTGC | 23607 |
rs571734432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47545305 | GGAAGCAAACTGCTC[C/T]AGTAGGACCTGGGAG | 23607 |
rs571750218 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47584513 | AATCAAAAGTTCAAA[A/T]TCAAGGCCCTCCAGT | 23607 |
rs571774175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47511940 | GAGGTGGGCGGATCA[C/T]GAGGTCAGGAGATTG | 23607 |
rs571838395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47511290 | GAAAACCTCAGACAA[A/G]CTAAATTGAGAGACA | 23607 |
rs571893135 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47493370 | TTTTTTTTTTTTCCA[A/G]TGCTTTAAATATTTT | 23607 |
rs571914830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47591118 | CACATACCATGTTAC[C/T]ACGTAGCAACAAATA | 23607 |
rs571993705 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47536840 | AGATAATGGTAAAAT[A/C]TTGTGTTTAGAGAGT | 23607 |
rs572020748 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47570100 | CTTTAATGGTGAACT[C/T]GGATTGATTCTATTA | 23607 |
rs572055791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47487655 | AGATCGCGCCACTGC[A/G]CTCCAGCCTGGGTGA | 23607 |
rs572058003 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47479319 | TTAACAAATGATTTA[A/G]AAGCAGGACGAATAC | 23607 |
rs572061096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47605818 | TAAGAAGTAGATCTT[C/T]GTTAGGAACTTAAGA | 23607 |
rs572074380 | snp | C/G | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521747 | TGAGATTTAAGATAA[C/G]TCTCACGCCTGTAAT | 23607 |
rs572076694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47518612 | TGTCATAAACAATGA[C/T]ATATGCCTCTTTGTG | 23607 |
rs572086396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47569337 | TTATGATTAGTCTCA[A/G]TTTATTGGAGATAGA | 23607 |
rs572091824 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47490450 | TTAAAAATAATTTCT[A/G]GTGTTTTCTTGAAGT | 23607 |
rs572125537 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47531779 | GAAGTATGTTTTATA[A/G]GAATCCTTTTCGGCC | 23607 |
rs572148279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47583681 | TCACTGAGGGACATC[A/G]TGATTGCTTCTAAGT | 23607 |
rs572235260 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47545155 | AAAATAGATCATGGA[C/G]AGGAGGCAGGACTAG | 23607 |
rs572276277 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47615667 | CTCTCACCTGGCCCC[A/T]CCTCCAACACTGGGG | 23607 |
rs572279680 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47576943 | TTACACAAGATAGAG[A/G]CTAAATAAGTATTTG | 23607 |
rs572308950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47504690 | AGGGGTACCTTGGAG[A/G]TACTGCAGGTTCAGT | 23607 |
rs572425310 | snp | C/G/T | 3.29866e-05 | 0.00406108 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47579402 | GACTGGAGAAGCTGG[C/G/T]TGGTGGAGGGGCGAA | 23607 |
rs572431029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47489431 | TCTGCCCGCCTCGGC[C/T]TCCCAAAGTGCTGGG | 23607 |
rs572445841 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47505428 | CTCCCATGTCTACCT[C/T]TTTCTACACAGACAC | 23607 |
rs572457348 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47495337 | TAGAGGTTGGAGTTA[C/T]GTAAGCAAAGGAACA | 23607 |
rs572457466 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47519651 | CCTTGTATGTAGATA[A/C/T]ATAGTGGAATTTATT | 23607 |
rs572479883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47571261 | AATACACTTCTGGCA[A/G]TGCAGGAGCAAGATG | 23607 |
rs572480952 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47537080 | GTGTAAAAGATACAT[G/T]GAGATTGATACTGAT | 23607 |
rs572492424 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47573102 | AAAGTACATAAAAAT[-/G]AACCACACAGTTTTC | 23607 |
rs572518319 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47527114 | AAAAGACTCCCCCCC[A/G]ATTGAAAAATATTCA | 23607 |
rs572522042 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47556638 | ACAGGCGGGAGCCAC[G/T]GTGCCCAGCTGAACT | 23607 |
rs572540789 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47578946 | ACAGGTGTGAGCCAC[C/T]GTACCCGGCCTCATT | 23607 |
rs572563765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47515943 | ATGCAAAATATGTGG[A/G]AAAAAAAGTAAAAAT | 23607 |
rs572573081 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47497704 | CAGGTGTGAGCTGCA[A/G]CTGCACCCGGACAAT | 23607 |
rs572580668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47574854 | TAAAACCTTAAGCTG[C/T]TAATTTGGTGGTAAA | 23607 |
rs572596863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47622302 | CTTGGTTCTTCCCTC[A/G]CCTGTGGAGTCTGCA | 23607 |
rs572611009 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47586419 | TGACAATATCAAGTG[C/G]TTTTACTTACCTGTA | 23607 |
rs572617295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47481705 | ATATGCACTTCTATA[A/G]TAGAGTGATTTCTTT | 23607 |
rs572632126 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47610436 | AAAAAGTATAAAAGA[A/G]CAAAAAATAAAAATA | 23607 |
rs572636285 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47556229 | CCTCACCCCCCTCCC[A/C]CTGATAGGCCCCGGT | 23607 |
rs572661830 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47549187 | TCTTCAACATAGTAC[G/T]GGAAGTCCTAGCCAG | 23607 |
rs572676360 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47599908 | TCTAACCCTTTTGCT[A/C]ATTTTTTTTTAAGCT | 23607 |
rs572687654 | snp | C/T | 1.65405e-05 | 0.00287576 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47503284 | CCCTTTTTTAGTTGA[C/T]TATATTGTGGAGTAT | 23607 |
rs572696031 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47603696 | TTTTTTCCTGTTTTG[A/T]AAAATAATTATTTTG | 23607 |
rs572703532 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47587323 | TGGGGCGCAGAAAAG[A/G]GCTACTTAGAAACCA | 23607 |
rs572704945 | in-del | -/CAC | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47531214 | TCTTGGTTTACACAA[-/CAC]CATTATTGTCTCAGT | 23607 |
rs572731583 | in-del | -/CA | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47519507 | CCTTGCCACTATATC[-/CA]CACACAAGTACCTGT | 23607 |
rs572740913 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47554059 | CTGGGACTACAGGCG[C/T]GAACCACCATGCCCA | 23607 |
rs572759210 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47563019 | TTCAAATGCAAGAAA[G/T]GAACAAATAAAACTT | 23607 |
rs572761352 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47477872 | AGGGGCGGGCTCCGA[A/G]GCTAGGCGGGCGCTC | 23607 |
rs572767908 | snp | A/C/T | 0.00279258 | 0.0372817 | intron-variant | CD2AP | GRCh38.p7 | 6:47545820 | AGAGGGAGAGTACTA[A/C/T]GTAAAGGAGCACCCC | 23607 |
rs572769992 | in-del | -/T | 0.409552 | 0.192466 | intron-variant | CD2AP | GRCh38.p7 | 6:47497147 | TATGACCATGTCGTG[-/T]TTTTTTTTTTACTGT | 23607 |
rs572797984 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47496703 | CTCATTGTTCTCTGC[C/T]TCTATTCTCATTCTC | 23607 |
rs572804004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47544931 | AAAATTAATGAAATC[C/T]AAGTAGTTAAGAACG | 23607 |
rs572845460 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47530552 | TATTGCTGAGTAGTG[G/T]TCCATTGTTTATTCA | 23607 |
rs572864391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47529916 | TCCCTTCCTTCCATG[C/T]TCCAGGCAAATTTAG | 23607 |
rs572871993 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47582442 | TACATATTATTTAAT[C/T]TCACTGCATGTGTTT | 23607 |
rs572890829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47581611 | TGGTAGCCACTAACC[A/G]TGTGTGGCTTTTAAA | 23607 |
rs572912625 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47500576 | TATAGTTAAAGGTGG[G/T]TAATCTAGCAGTTTG | 23607 |
rs572962228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47493685 | TGGAATTCCAATTAC[A/G]TGTGTTTATACCTCT | 23607 |
rs572962812 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47601389 | TTTCAGGCTGCTGTT[-/C]TTTATTCCTTCCACT | 23607 |
rs572969485 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47606445 | GAGAGAGGTGTGTTC[A/C]TTCCAACAGGGTCTG | 23607 |
rs572979755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47558845 | GGCATCATAAAATGA[A/G]TTACGGAGGAGTCCT | 23607 |
rs572996510 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625161 | TATCTTGTCACTTAG[C/T]TCTTCATGTTTCTCC | 23607 |
rs573017912 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47501106 | AATTCATTCATCTCA[G/T]CTGGGCATGGTGGCT | 23607 |
rs573019175 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47481288 | GGCGGTGAACTTTTT[-/A]GTTTATTTTATAGGC | 23607 |
rs573022895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47485348 | CTGATCTTTGCAGGC[C/T]TAGGCTAATGTGTGT | 23607 |
rs573060654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47588160 | GGTTTTTCTCATCTT[C/T]TAGATTCCAGCTTAA | 23607 |
rs573065890 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47602322 | TGTTAAGAACCATGC[A/T]TACAATTTTTTTTCT | 23607 |
rs573095401 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47552423 | ATTCTTGAGTTACTT[C/G]ACTTAGAATAATAGC | 23607 |
rs573114761 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47494958 | TGAGCCAAGGAGTTC[A/G]AGACAAGTCTGGGCA | 23607 |
rs573149028 | in-del | -/AA | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47607056 | ATAGTGAGAATATGC[-/AA]AGTTTGTTCTTCTGT | 23607 |
rs573182810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47604557 | CAGGCTAAAATGATT[A/G]GATTGTACTTGTTAA | 23607 |
rs573192904 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47553438 | TGCAACCTCCGCTTC[C/G]CAGGTTCAACTGATT | 23607 |
rs573205891 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47602911 | TCTCAAAAATAAACA[A/C]AAAAAAAGCAATTTT | 23607 |
rs573254648 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47562093 | TTTAAGGAAATTTAA[G/T]TTTTCTTCCAAGTTT | 23607 |
rs573261967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47498280 | TTAATTTTTCTTTTT[C/T]TAGAATCCAGTATTG | 23607 |
rs573275712 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47510309 | TGCTGAGAGGGCCTA[C/G]AAGCAGTGATACCTC | 23607 |
rs573283984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47565476 | ATACTTGTCTTTTCC[A/G]CCCTTTTCTAAAAGT | 23607 |
rs573307228 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47523523 | ATAAAAATAAAAAAC[A/G]GTTGAAAGAATGCCA | 23607 |
rs573326328 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47502936 | AAGAGAGAGAATTAC[A/T]TAAGGACATGAATAC | 23607 |
rs573379058 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47523983 | TTGGTAGATAGCTTT[A/T]AAGACTGTTTCCTAT | 23607 |
rs573382826 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47504212 | TTTTCTGTGTATTAG[G/T]TTTCTTACATCCAGC | 23607 |
rs573441990 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47531442 | ACTGTTGCGGGAAAC[C/T]GAGGACTGGAGAGAC | 23607 |
rs573444365 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47501002 | TCCGCCTGCCTCCGC[C/T]TCCCAAAGTGCTGGG | 23607 |
rs573455091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47478318 | GCTGTGCCCTTTCTC[A/G]GCCTTCTGGGGAGGC | 23607 |
rs573461948 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47571207 | ATATTGCTTTGTCCA[A/G]CAGGCTGGTTATTGG | 23607 |
rs573466665 | snp | C/G | 0 | 0 | intron-variant | CD2AP | GRCh38.p7 | 6:47515643 | TTATTAGAGAAATGT[C/G]ATCATTCTGTAACGT | 23607 |
rs573469008 | in-del | -/TAAGC | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47489098 | TGAGTTATCTCGATT[-/TAAGC]GCTTAGTCAGTTACA | 23607 |
rs573473777 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47611475 | AGTTCAGAGGTTTTC[A/G]CTTTACTCTTATAAT | 23607 |
rs573523157 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | CD2AP | GRCh38.p7 | 6:47557318 | TTGCTGTGCCGAAGC[G/T]CTTTAGTTTAATTAG | 23607 |
rs573524950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47578569 | ATTTTTAGTATATAA[A/G]GTGTTAAAAGTGTTA | 23607 |
rs573549931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47517346 | GGAGTGCAGTGGTGC[A/G]GTGCGATCACAGCTC | 23607 |
rs573608698 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47556903 | AGGAATTGCCACATT[A/G]TCTTCCACAATGGTT | 23607 |
rs573609250 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47516285 | TAGTCTTGTGGCAAG[A/T]CATTGTCAATTTGTG | 23607 |
rs573645767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47549500 | ATGCTTAGGAATATA[C/T]CTAACCAAGGAGTCA | 23607 |
rs573660877 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47535255 | AAACTGCAACCTCTG[A/G]CATAAATGGGTTAAT | 23607 |
rs573687700 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521318 | GCATTTTGGGAGGTC[A/G]AGGCGGGCAGATCAC | 23607 |
rs573688270 | snp | C/G | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47477111 | TTCACATTGACGCTA[C/G]AAAAAATGCCTGGCA | 23607 |
rs573724319 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47564914 | ACTATATTTGATTAT[A/G]TCATATAGTTTCTCC | 23607 |
rs573763382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47514659 | TAACAGTGTAAAACA[A/G]GATAAATTGTAATGC | 23607 |
rs573809541 | snp | A/T | 0.0670745 | 0.170406 | intron-variant | CD2AP | GRCh38.p7 | 6:47615800 | TTAATTTAATTTATT[A/T]ATTTATTTATTTATT | 23607 |
rs573829858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47481511 | CCACCATGCCCAGCT[A/G]ATTTTTGCATTTTTA | 23607 |
rs573835656 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47607237 | TTGATTCCAATTCTT[G/T]GCTGTATTCTTGTGA | 23607 |
rs573840737 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47598741 | TACAGTGGACTTTGG[A/G]GACTTGAGGGGAAAG | 23607 |
rs573848624 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47491750 | TGCATGTAATAATTT[A/T]AAAAAATTATGGATT | 23607 |
rs573867864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47518916 | TGGTATTTTTTAGAA[A/G]GAGACACGGTAGTAC | 23607 |
rs573906380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47594025 | AACATTGGGCTAAGC[A/G]AAAGAAGCCAGACAC | 23607 |
rs573915226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47621749 | CTGTTCAGGATCTCT[A/G]ATTCTTCCTGATTTA | 23607 |
rs573966857 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47591687 | AAATGGGTTAACTTA[C/T]TACGTACAGTGTTGG | 23607 |
rs573983223 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47544032 | GGTTGAGAACACAAG[C/T]GCGAATGGTTATAAA | 23607 |
rs574001778 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47479327 | TGATTTAGAAGCAGG[A/G]CGAATACAGACTACT | 23607 |
rs574012278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47519607 | CCTGTTAGGATTGTT[C/T]GGTAGCAATTAGATT | 23607 |
rs574042668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47573691 | AGACGGGGTTTCACC[A/G]TGTTAGCCAGAATGG | 23607 |
rs574068410 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47558551 | TGTTGAATTTTATCG[A/C]AGGCCTTTTCTGCAT | 23607 |
rs574084146 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47524852 | ACTTTCAAAGTAGGT[C/G]TGCTATATCTGTCAT | 23607 |
rs574095203 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47608890 | GGATTTTTCTTTCTT[C/T]CTTTTTTCTTCTGTT | 23607 |
rs574127575 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47627219 | AAATTATATTACTTC[A/G]ATTTCCAAATACAAG | 23607 |
rs574155963 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47517840 | TCTGCTGAAAAAAGG[G/T]ATATTAATAGTATTT | 23607 |
rs574175207 | in-del | -/AATAC | | | intron-variant | CD2AP | GRCh38.p7 | 6:47537621 | GTATGCTACAGACAT[-/AATAC]ATTACCTCTGATCAC | 23607 |
rs574190129 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47620573 | AGAATTGTTTTTTCC[-/A]ATTCTGTGAAGAATG | 23607 |
rs574216100 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47525582 | GATTATTATATGGAC[A/G]TATTACAACATGAAG | 23607 |
rs574243338 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47489044 | GTTGTCTATATAACT[A/T]AATTATGTTTTAAAA | 23607 |
rs574264490 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47543868 | TATCTCACAAGCTCC[C/G]AGGTTACACTGTTGC | 23607 |
rs574299694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47597164 | GGGAATTATAGTACA[A/G]ATCCAGTCAGGGTTG | 23607 |
rs574312323 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47568630 | GCACCTGTAATCGCA[G/T]CTACTTGGGAGGCTG | 23607 |
rs574314971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47579521 | CAATGATGATAATAC[C/T]TGAAAGAACATTTTG | 23607 |
rs574323467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47543229 | GAGTGTCTTCTAAGC[C/T]GAGAAGTGAAGATGA | 23607 |
rs574346347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47619950 | GTTAGGGTTTGTTGT[A/G]GATTCTGGATATTAG | 23607 |
rs574412982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47510546 | CTGAAGGAGCTCCCA[A/G]TATCTAGAGCTGGAA | 23607 |
rs574442700 | snp | A/G | | | intron-variant, downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47604296 | AATGTGCACTGTTCC[A/G]TTTTACTAACCTAAT | 23607 |
rs574442886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47576748 | AGGTCAAGGATTTTG[A/G]TATACTTTGTTGGTT | 23607 |
rs574445338 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47561803 | ATGTATTTATTGAGA[C/T]GGAGTCTCGCTCTGT | 23607 |
rs574472490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47540778 | AGAAACCACATTTTA[A/G]AAAAGGTCTGAAATT | 23607 |
rs574481335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47620721 | GTCTGTGATTTCTTT[C/T]AGCAGTGTTTTGTAG | 23607 |
rs574500344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47486443 | GAGAGAGAGAGTATA[A/G]GGTCAGTGTCAGAAA | 23607 |
rs574506133 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47546361 | GGGATTATGTTAAAC[A/G]ACCAAACGTAAGAAT | 23607 |
rs574509354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47576123 | CATGTCATCCAGGCT[A/G]GAATGCAGTGGTACA | 23607 |
rs574521436 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497208 | TCCTTTCCCCTTTTT[C/G]CTTTCCCCTTTTTCC | 23607 |
rs574525000 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47537993 | TGGCCTCAAGTGATC[G/T]GCCCGCCTCAGCCTC | 23607 |
rs574537336 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47548998 | ACATTAGACAAAATC[C/T]AGCATCACTTTATGA | 23607 |
rs574553566 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47589531 | GTACACACATATATA[C/T]ACATATGTACACATA | 23607 |
rs574576741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47577956 | GTTTTATTGTGTAAA[A/G]TATAATGATGTTATA | 23607 |
rs574581072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47569292 | GAATTTATCCAGAAG[A/G]TGGAGGAAATGCGTT | 23607 |
rs574589324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47487001 | TTTATTTAGAAGTAC[A/G]TTCTCCTGAGATCCA | 23607 |
rs574628789 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47531705 | GTAATAATTATAGTA[C/T]ATAATAGTTATTTTG | 23607 |
rs574661177 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47530771 | TGAAAATGCTAAAGA[A/G]CAGAAAGGTGATACT | 23607 |
rs574665112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47546867 | TAGAAGGGATTTTCT[A/G]TCTTGAGCCTCCTCA | 23607 |
rs574689558 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47590353 | ATATATAAATATATA[C/T]ACACAAATGTTAATA | 23607 |
rs574753039 | in-del | -/TAA | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47608803 | TATGAAAGATCAAAG[-/TAA]TACCTTTATAATGCT | 23607 |
rs574781689 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47539826 | GATTTTTAGAAGACA[A/G]TTTTTGTACAATTAA | 23607 |
rs574784132 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47591793 | TTAGACATTTTTGTT[A/T]AAAAAATTATATACC | 23607 |
rs574791940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47481032 | AAATGCCTATTGAGA[A/G]GTTTGAGGTATTCTG | 23607 |
rs574832947 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47524908 | CTATTGACACTTAGA[C/T]GATACGTACTGATTT | 23607 |
rs574834425 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47582640 | CTATTTTAGAATGCT[A/T]TTTGTTTCTTCCTCC | 23607 |
rs574836403 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47488833 | AAGGTCGAGGCTACA[A/G]CGAGCCATGATTGTG | 23607 |
rs574925322 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CD2AP | GRCh38.p7 | 6:47585121 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 23607 |
rs574936963 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47526431 | GAAGGCTGTAAACCT[G/T]AGTTTTTTCTATTCA | 23607 |
rs574962678 | in-del | -/AA | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47573097 | CAGAAAAAAGTACAT[-/AA]AAATAACCACACAGT | 23607 |
rs574974824 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47511115 | AGGAATAGATGGACA[A/G]GGAAAAATAGTAGCT | 23607 |
rs574975034 | in-del | -/CCCCC | 0.167484 | 0.23599 | intron-variant | CD2AP | GRCh38.p7 | 6:47529184 | TTAACTCTAGTACTG[-/CCCCC]CCCCCCCCCCCCAAC | 23607 |
rs575011274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47562658 | GATGTAATGGATGTT[A/G]ATACTGCCACTGCTT | 23607 |
rs575081036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47605656 | GGTACATTAAATCAT[A/G]CTTTTGCTTTATATT | 23607 |
rs575094498 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47597290 | AGGTAGAAGGCCCTC[G/T]CCTGCCACCCAGACA | 23607 |
rs575101512 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47544818 | CTGTTGTCACTTTTT[A/T]AAAAAAATGGTATAG | 23607 |
rs575103366 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CD2AP | GRCh38.p7 | 6:47586706 | TGGTAGAAGGAAAAC[A/G]ATACTAGATTGGCAG | 23607 |
rs575110583 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47496325 | TTGTTGCTAAGTCAC[A/C/T]CATTAGTCTGAATGT | 23607 |
rs575142244 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47592938 | ACCCAAGGAGTGATC[A/C]TGGGAATCCCCAATT | 23607 |
rs575142405 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47595020 | TAGGAGCTTCTTATT[G/T]TTGTATATACGTCTT | 23607 |
rs575155906 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47555498 | TTTTATGATTAGTTG[G/T]ATTTATAGGTATTAG | 23607 |
rs575168292 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47583140 | AGGTTCACAGCAAAA[C/T]TGAGCCAAAAGTACA | 23607 |
rs575179382 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47558793 | ATTTTCTTTTTTTTG[A/T]TGTGTCCGTGCCAAG | 23607 |
rs575185257 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47500200 | ACCCTTCAGTTTTTT[C/G]CCTTGGAAGGAAAAT | 23607 |
rs575236880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47544075 | AATAAATGAAGCTTG[C/T]TTGAAAAGCTAAAGT | 23607 |
rs575237015 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47613088 | TTCGATCCACTTTTA[A/C]TTCTCATTGTCTTGC | 23607 |
rs575282952 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CD2AP | GRCh38.p7 | 6:47564818 | ATAATTATGTTCCTC[A/G]TAGCTGTTAGAAAAA | 23607 |
rs575284881 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47588711 | GAATTATATCTTTCC[A/G]TTCTGCCATCCTCAG | 23607 |
rs575285884 | in-del | -/T | 0.00993419 | 0.0697739 | intron-variant | CD2AP | GRCh38.p7 | 6:47489488 | GCTGCACTCGACTAG[-/T]TTTTTAAAAAATAAA | 23607 |
rs575307807 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47502115 | ATTCATTTACTTTTG[G/T]GTTGTTGGAGTAAGG | 23607 |
rs575308251 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47613851 | TGTTTCCTGTAGCCA[A/C]CTCCCGTCTTAGCTA | 23607 |
rs575343143 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47513907 | TGGGGGGGGGGCTAG[C/G/T]CTTACAGATGTACAG | 23607 |
rs575347446 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47616619 | TACTTGACTTTTTCC[A/T]TTATTCAGAATCAAA | 23607 |
rs575368075 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47603606 | AAACCTAATATACAT[C/G]TTGTGTAAGTTAGAT | 23607 |
rs575380735 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47565604 | CTCCATGTAATCTTC[A/C]CCATCTGAGTTAAGG | 23607 |
rs575453341 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47581579 | GAAAGCTTTTTATAT[A/T]GCTTTACTCTTCAAT | 23607 |
rs575465322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47594396 | CCAGGAATGATGAGT[C/T]GTATTTTTGTTACCT | 23607 |
rs575483647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47507592 | CTTGGATTACAGGCT[C/T]CCACCACCACGCCCA | 23607 |
rs575491017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47610164 | CCCCTCTGGCTTTTT[A/G]AATGAAGAAATTGAC | 23607 |
rs575506129 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47608739 | ATTAAATTGTTCACA[A/G]TTACTTTTAAGTGAA | 23607 |
rs575541691 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47564511 | TTAGTAACTGCGCAG[A/G]ATTTTATCTGTTAGA | 23607 |
rs575549235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47508988 | TTTTGGCCTATCTCA[A/G]CTTTCAGCATTACTT | 23607 |
rs575554834 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47622623 | GTTTCTCCAGTGCGG[G/T]GTGTGTGTTCGGGAG | 23607 |
rs575572081 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47620150 | TGTGCCAATAACTAG[A/G]AGGGTTTTTCTGTTG | 23607 |
rs575582318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47560020 | TCCCATTCCTCTATA[C/T]ATTTCCATACTATTA | 23607 |
rs575595231 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47516204 | ATCCTTTCATGCAAA[C/G]TTTGGTCCAGCTAGC | 23607 |
rs575629845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47614747 | TATCTGTGAAGCACA[A/G]CAAAACGAAGTACAA | 23607 |
rs575643051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47601501 | ACTGTCAGATTATTC[A/G]CTGAGCAGGTTTTAT | 23607 |
rs575658486 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47481961 | ATACAGGCTCTCCCT[C/G]TCTTGCCCAGGCTAG | 23607 |
rs575675814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47552725 | CTGATGTTTCTCTCC[A/G]TTTGTTGTATTTATT | 23607 |
rs575703614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47505474 | TCTCAATCTCTTCCC[C/T]GCCTTTCCCGCCCTT | 23607 |
rs575743490 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625090 | ATATAAAATATGTAA[A/G]CACCAGCCTGTTGCT | 23607 |
rs575762467 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47478708 | GTTTAAGGAGAGAGA[G/T]AAATTTGTTCAAAAA | 23607 |
rs575813652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47553290 | TCTTTTTCTAGCTAT[A/G]TTGTGTGTAGTGCTG | 23607 |
rs575822969 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47507396 | CTCTAGAAACCTTTC[C/T]GGGAGGTTTTCAATT | 23607 |
rs575824882 | snp | A/G | 0.000291049 | 0.0120598 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624278 | TTCAGAAGCAACGCT[A/G]TGAACTTCAGCTGAC | 23607 |
rs575844794 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47567244 | GTTCAGCTCTTTGAG[G/T]GTTGTGAGTAGTAAT | 23607 |
rs575853103 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47618170 | CTAAAAAATATAAAA[A/C]TTAGCTGGGCATGGT | 23607 |
rs575857118 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47531802 | TTTCGGCCGGGCGTG[A/G]TGGCTCACGCTTGTA | 23607 |
rs575890686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47529855 | AGCTTTATATCAGCC[A/G]TCTGCTCGCCTTGCT | 23607 |
rs575892824 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47522003 | CTGGGCAACAAGAGC[A/G]AAACTCTGCCTCAAA | 23607 |
rs575910800 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47480254 | TTGGTCATGTAATAA[A/T]AAAATTCCCAAGTTC | 23607 |
rs575922448 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47561461 | TGGAATCAGCTACCT[A/G]TCAAGGCAAACTTTT | 23607 |
rs575936155 | snp | C/T | 0.00636936 | 0.0560724 | upstream-variant-2KB, utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47477772 | CTCCCGGTCCCAGCT[C/T]CCCGCACCTTCTCGG | 23607 |
rs575941478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47519386 | TGGGTTTCTAGCTAC[C/T]CTACTAGAGCTACTT | 23607 |
rs575972265 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47577794 | TGTTGTCCAGGCTGG[A/T]CTCAAACTCTTGAGC | 23607 |
rs575982719 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47517737 | CAATCTGGTATATAG[C/T]TTAGGTATTTAGACT | 23607 |
rs575985519 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47512019 | AAAAATTAGCTGGGC[C/G]TAGTGGCGGGCGGCT | 23607 |
rs576006684 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47563425 | AATCTGCAACTTTCT[A/T]ATTCTTGAAGAGGCA | 23607 |
rs576014538 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47527820 | ATTTTTGAAAGTGAC[A/G]AGGTTTAGTTTTCTA | 23607 |
rs576057529 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47510515 | GGGCCTGTGTCAAAG[A/G]GACTTAGAACCCAAC | 23607 |
rs576062130 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CD2AP | GRCh38.p7 | 6:47599976 | AATCTGTACTTCCTG[C/T]TTTTTTTTTAATACC | 23607 |
rs576130344 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47537764 | CACTTAATGGCCTAA[A/G]CATTACGATTTTTTT | 23607 |
rs576200803 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47556785 | TGCTGCATTAAACAT[A/G]TGTGTGTGTGTGTCT | 23607 |
rs576214994 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47540268 | CCTTTTATTGACACC[C/T]CTCTTCTTTTTTGTG | 23607 |
rs576240253 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47488817 | CATTACTTGAGCCTG[G/T]AAGGTCGAGGCTACA | 23607 |
rs576244550 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47598519 | TGCCCATGAATCAAC[A/G]AGTGAATAAAGAAAT | 23607 |
rs576265618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47570209 | TTTTCTCCAAACAAG[C/T]AATTGCATTTTGCAG | 23607 |
rs576291141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47533233 | GCAACAGAAAGTGTA[C/T]GGTCTGCAAATTGTA | 23607 |
rs576303880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47480900 | TTGGATGTACTGTGC[A/G]AAAGTCCATTATTGG | 23607 |
rs576348860 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47532440 | CTTGCCATATCAAGT[A/T]AAAATTGTTAATTTT | 23607 |
rs576375023 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47585109 | CCATCCTGGCTAACA[C/G]GGTGAAACCCCGTCT | 23607 |
rs576403036 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47534589 | ACTTGCCTGTAATTC[C/T]AGCTACTTGGGAGAC | 23607 |
rs576425389 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47616670 | TAGCTGCCTTCTTGA[G/T]GTACTGCAGTTACTT | 23607 |
rs576442218 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47513504 | GGTATTTTTAGTGTT[G/T]GATTTTGAAGTTTTC | 23607 |
rs576463581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47579855 | TGGATATTGCTGTTA[C/T]GCTGTTGGTGCATTT | 23607 |
rs576464218 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47623102 | CAGTGCTGCTAAAAC[A/G]TTGAGCTAATCATCA | 23607 |
rs576476884 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47565141 | GTTTTCATTGAAGAA[C/G]TGTAGGATAAAAGTT | 23607 |
rs576479588 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47537872 | CTGCAGCCTCAGCCT[C/G]CCCAGTAGCTGGAAT | 23607 |
rs576500118 | in-del | -/GAAAAA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47543186 | AAGAAAAAGAAAAAA[-/GAAAAA]AAAGAAAAAGAAAGC | 23607 |
rs576507174 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47603009 | TTTATTTGATATTTG[A/G]TAGTTGATCTATTTT | 23607 |
rs576534180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47489477 | CACCGTGCCCGGCTG[C/T]ACTCGACTAGTTTTT | 23607 |
rs576578829 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47490175 | AACTGTAGACATAGG[G/T]TCTTGCCATATTGCC | 23607 |
rs576582275 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47511872 | ACTCTACTAAAATAC[-/A]AAAAATTGGCCGGGG | 23607 |
rs576589084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47592527 | AGCTCCTAAAACCCT[C/T]GAAATTTCCTGAGTG | 23607 |
rs576598218 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47481327 | ATAAAACATATCAGT[C/T]ATGTGGTGGTGTTTT | 23607 |
rs576637934 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47502485 | CCTGGCTGGCCTCGA[A/G]CTCCTGAGTTTTTTT | 23607 |
rs576669830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47543126 | ACCGCACTCCAGCCT[A/G]GGCAACAGAGCAAGA | 23607 |
rs576692064 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47627140 | GATTTTATTGCCAGT[C/T]GTGTCAGTCTTTATT | 23607 |
rs576716733 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47610239 | TTTCTATAACCACTA[G/T]TATTTGAATTTTAAA | 23607 |
rs576720204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47501174 | GGAGGATCGCTTGAG[C/T]CCAGGAGTTTGAGAG | 23607 |
rs576738448 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47537162 | TTGAAACAATGCCAG[C/T]CTACACATTACTTCA | 23607 |
rs576753032 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626145 | TTCAGGCTGTTCTTA[A/C]AGTTTTTGTTGGTCA | 23607 |
rs576821243 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47516334 | ACAGAGCAACAGAGC[A/C/G]TAGAAAATCACGTTC | 23607 |
rs576836133 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47619749 | GTTTTTTGATTTTTT[G/T]ATTATGGCCATTCTT | 23607 |
rs576846291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47568074 | AAAGAACAGGACCTA[A/G]TGATAATGTTATTTG | 23607 |
rs576853830 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47576073 | TTTTATTTATTGTAT[G/T]TGTTTTATTGTAGTT | 23607 |
rs576856014 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | CD2AP | GRCh38.p7 | 6:47486389 | AAGACAACATAATAA[C/G]AATGAAAGTTAGTAT | 23607 |
rs576885629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47524049 | TTCCCCCTTTTACAT[A/G]CTATTCTTCATACTG | 23607 |
rs576911152 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47584455 | GTGAATGTCTAGTTG[A/C]TCCAACACCGTTTGT | 23607 |
rs576930415 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47611986 | AGTTGAGGAGAGACT[A/G]TTGGCTAGAGTTTTT | 23607 |
rs576936201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47545609 | TTCATTTCAATACCC[C/T]GCCCGCTGGTCCCAA | 23607 |
rs576941346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47553211 | TAGATGACTAACTTA[A/G]TAAAAGGTTGCCTAC | 23607 |
rs576954086 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47595774 | TCTGCCTCTGTCACA[C/G]TTTTCCAGCCTGATA | 23607 |
rs576955427 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47541968 | CTCCTTAGAGTCCTT[C/G]TATCACCAAATCCTA | 23607 |
rs576957152 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47603499 | CTGTCTTGGTGTTCA[A/G]TGAGTAATAAAACAG | 23607 |
rs576984094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47485433 | GCTTATAGAATATGA[A/G]TATAAGGAAAGAAAA | 23607 |
rs576987507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47494654 | CTCTTTACTGTGAGA[A/G]TCTGGCAGTACCATA | 23607 |
rs576991460 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47491994 | TTACCTGTTTTCAGT[C/T]GAGATTTCCTTTTTT | 23607 |
rs577015380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47619201 | TACTGCACCACGTTC[A/G]TAGTCTTTCATCCCT | 23607 |
rs577058736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47478391 | TTCTCCCCACCGCCC[C/T]TTCTTGCCCTGCCTT | 23607 |
rs577061929 | snp | A/G | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521445 | TAATTCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 23607 |
rs577077859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47545955 | ACAAGGTTCTTTACC[A/G]TTCCCCAAAAATCAC | 23607 |
rs577095249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47596159 | TTTAAAATTGACATA[C/T]ACAATTGTGTGTATT | 23607 |
rs577107810 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47607306 | GATATACAGATTTCC[-/T]TTTTTTTGGTATATA | 23607 |
rs577112744 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47562339 | CAGGAAAAAATGTTA[A/C]TTTACATAGTCATAA | 23607 |
rs577116820 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47554545 | TTTATTTCATAGTGC[C/T]AATTTTGTGCCTGTT | 23607 |
rs577125087 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47496233 | GATATTTTCTTGGGT[A/G]TAGAGAGTTTAAGAT | 23607 |
rs577174924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47589468 | TATATACATATATAC[A/G]CACACATATACACAT | 23607 |
rs577180447 | snp | A/G | 0.00636936 | 0.0560724 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476150 | GCCTCATTCTTCCAA[A/G]TCGTAAATGGCCTTC | 23607 |
rs577181589 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47534621 | GAGGCAGGAGAATCA[A/C]TTGAACTCGGGAGGT | 23607 |
rs577208478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47593518 | GAAAAGATGTTTAAC[A/G]TCATTAATCATGTCA | 23607 |
rs577254196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47558122 | TCATGATTTGGCCCT[C/T]TGTTTGTCTTTTATT | 23607 |
rs577283200 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | CD2AP | GRCh38.p7 | 6:47562157 | GCCTTGTTCGTTTGC[-/T]TTTTTAGTATAAAAG | 23607 |
rs577285557 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47587521 | TGTTTTCATTTTCCC[A/C]GAAGTACCTAAAATC | 23607 |
rs577316666 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47503781 | TCTCATTTGAGCCTA[C/T]AGTATACTTGTGAAA | 23607 |
rs577344618 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47594211 | GGTGGTTGCGTAACA[A/T]CGTGAATGTACTAAA | 23607 |
rs577349177 | in-del | -/T | 0.432504 | 0.170857 | intron-variant | CD2AP | GRCh38.p7 | 6:47567084 | TTTCTGATTTCCCAG[-/T]TTTTTTTTTTTTTAA | 23607 |
rs577358364 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47561523 | ATCAAGATCTGGGTA[G/T]AGGTGTGGTCATTGC | 23607 |
rs577364777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47517170 | TCTCACTATGTGATG[C/T]GCCTGCTCCCCTTTC | 23607 |
rs577384954 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CD2AP | GRCh38.p7 | 6:47568537 | ACAAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 23607 |
rs577434644 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CD2AP | GRCh38.p7 | 6:47511029 | AATGAGCTGAGATCG[C/T]GCCACTGCACCCCAG | 23607 |
rs577440629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47597333 | ACAGAGCAGCTGAAC[C/T]CCTCCACTAGCTTTC | 23607 |
rs577476928 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47525482 | GTTTTTATTATTCTT[C/T]GCGACCTTTGAGTCT | 23607 |
rs577503717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47604639 | CACCCTTCAAATTAC[A/G]ACATATTTTAACATC | 23607 |
rs577505170 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47565539 | TTAGATGTCTAATAG[G/T]CATCTTAAACCTAAG | 23607 |
rs577507436 | in-del | -/T | 0.389152 | 0.207694 | intron-variant | CD2AP | GRCh38.p7 | 6:47585202 | AGCTACTCAGGAGGC[-/T]TGAGGCAGGAGAATG | 23607 |
rs577512360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47612182 | GAAAATGTATGATAG[C/T]CGAATATAGAAAATT | 23607 |
rs577524061 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CD2AP | GRCh38.p7 | 6:47499568 | CATGTAACCATTCTC[C/G]CATCTCTGTTGTTAC | 23607 |
rs577543842 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47478836 | GCACCTAAGCATTCA[C/G]TGTGCTCCCGAGGAC | 23607 |
rs577583675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47503105 | CTATATTAAGATATT[C/T]AAGAAATTTGCTGAT | 23607 |
rs577614099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47609444 | CACTTTGGGAGACCA[A/G]GTTTGGAGGATTGCT | 23607 |
rs577643999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47510353 | ACATCCAGTGCCCAG[A/G]TCTTGATTTCCAAAT | 23607 |
rs577673405 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47543985 | TGAAGATGGGAGTGA[C/G]TCTGAGTTCTCAGTT | 23607 |
rs577683871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47508899 | TTGGTGTGTTCACTG[A/G]AGTAGCACTTTTAAT | 23607 |
rs577717595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47507492 | TGGAATTTAGTGGGG[C/T]GATCTTGGCTCACTG | 23607 |
rs577747105 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47508228 | TAGAAGGTTTCATCT[C/T]CATTGAAAATCTGTT | 23607 |
rs577753924 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47489548 | ACATAGCAACTTCCC[A/G]TTTTTTGGTAATTTT | 23607 |
rs577754379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520495 | CATTAGTGCTGTCCA[C/T]ATGGCCTCCGCTGAC | 23607 |
rs577776807 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47572025 | CTCTCTGGCACATAC[A/C]GGATGTTAAGAAGCA | 23607 |
rs577822077 | snp | A/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47477048 | AATTATACTTCTTCG[A/T]AACTACCAAGCTCAT | 23607 |
rs577881700 | snp | A/G | 0.000798403 | 0.0199641 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47608013 | ATTAAAAAAAGATAC[A/G]TGCTACTCTCCAAAG | 23607 |
rs577886634 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47572491 | GATAATATTGAAAAT[G/T]GTTAGGGTAGATCAC | 23607 |
rs577888216 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47615843 | TATTAGCAGTGGTAC[A/G]AACTCGGCTGACTGC | 23607 |
rs577916567 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47537224 | TGCTTTCTTATTTTG[A/G]GTCAGTGCTGAAGAA | 23607 |
rs577949236 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47622725 | AGAGCAGTCCGCTTT[C/G]TTCAGAGGGTCTGTC | 23607 |
rs577949273 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47614928 | GGTGATTGGCAATTT[A/C]GACTATTTCCTTTAT | 23607 |
rs577962006 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47484284 | CCTTGGTTTTAACCA[C/G]AAATGAAGTAGGCAT | 23607 |
rs577962052 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476226 | TACTCTGTTTGCATA[C/T]CCACTTCCATTCCTC | 23607 |
rs577974457 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47596222 | ATATAATTCATTGTG[A/G]AATGGCTTCGGTAAC | 23607 |
rs577975559 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47507124 | GCCACTTTCTTTGCT[C/T]CTCCATAGGAAGCAA | 23607 |
rs577975761 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47513894 | AAAAATTTTTTTTTG[C/G]GGGGGGGGCTAGCCT | 23607 |
rs577983507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47574441 | TTCATGTTTGAATCT[A/G]ATAAAATTAGAATGC | 23607 |
rs577997907 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CD2AP | GRCh38.p7 | 6:47602937 | ATTTTAAAGAAACAC[A/G]TTATTCGATGGAAGC | 23607 |
rs578037228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47558932 | CCTCTGGTAGAGTTC[A/G]GCTATGAATCCATCT | 23607 |
rs578072282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47515307 | TTTAATAAATTAATC[C/T]GAATGAGAAGGAAAG | 23607 |
rs578083135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47566652 | GTCCTGGTGTGTGTT[C/T]CCCTACCTGTGTCCA | 23607 |
rs578104331 | snp | C/T | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521412 | CAAAAATTAGCTGGG[C/T]GTGGTGGCGGGCGCC | 23607 |
rs578119115 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | CD2AP | GRCh38.p7 | 6:47539830 | TTTAGAAGACAATTT[G/T]TGTACAATTAATTTT | 23607 |
rs578128552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47580115 | TAACTCTCCAACTCT[A/G]TGGAAGCTTAGGCTG | 23607 |
rs578152568 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521986 | TGCCATTGCACTCTA[C/G]CCTGGGCAACAAGAG | 23607 |
rs578205288 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CD2AP | GRCh38.p7 | 6:47528821 | TCACAGAGATTTTTT[G/T]GGATCTTTTGCCCAT | 23607 |
rs578214494 | in-del | -/T | 0.00597247 | 0.0543191 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624913 | TCAACTTTTAGAATA[-/T]TTTATGTTGCTTGCA | 23607 |
rs578236838 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47535634 | CCAGGGAATATTTGC[A/G]TATTATATATACTGC | 23607 |
rs578255344 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CD2AP | GRCh38.p7 | 6:47529308 | AAAAATTGGTTCCTA[C/G]CTGGGGCCACTGTCT | 23607 |
rs745308159 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47547729 | CAGAATATACATTCT[A/G]TTCAACAGTGCATGT | 23607 |
rs745318268 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47532582 | AATGAAGTTTGTCTG[A/T]TTATGGATTTCCTAT | 23607 |
rs745338788 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47479499 | TAACTTTCATACTCA[A/G]AAGTGCTCTTGAGCT | 23607 |
rs745345734 | snp | A/G | 1.64879e-05 | 0.00287118 | missense | CD2AP | GRCh38.p7 | 6:47609264 | AGAGCCCAGATTATT[A/G]AATTGTTGTGCATTG | 23607 |
rs745352714 | in-del | -/GTG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47481330 | AAACATATCAGTCAT[-/GTG]GTGGTGTTTTTTTGT | 23607 |
rs745360728 | in-del | -/A | 1.65348e-05 | 0.00287526 | frameshift-variant | CD2AP | GRCh38.p7 | 6:47607942 | CAACTCACAGCCCCG[-/A]AAAAAATCTTGAAGT | 23607 |
rs745362831 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47490850 | AGTACAAAGAGGAAG[A/G]GTGGGTTTTGTGTGC | 23607 |
rs745366835 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47559279 | TTTTTTTTTTTTAAC[A/T]GGCAGGGTTTCACTT | 23607 |
rs745386995 | in-del | -/AT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47621486 | CTGTGTTCATCAAAG[-/AT]ACTGGTCTGTAGTTT | 23607 |
rs745405189 | snp | A/G | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520084 | AGAAAAATGACCTGT[A/G]GAAATGATTTTTTTT | 23607 |
rs745407826 | snp | A/G | | | synonymous-codon | CD2AP | GRCh38.p7 | 6:47533703 | AATAAGCACCTATGG[A/G]CTTCCAGCTGGAGGA | 23607 |
rs745421771 | snp | A/G | 3.31011e-05 | 0.0040681 | missense | CD2AP | GRCh38.p7 | 6:47533692 | CTTGTACAACGAATA[A/G]GCACCTATGGACTTC | 23607 |
rs745454724 | snp | G/T | | | utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47478007 | CCGCCGTGGCTCCTG[G/T]GGAGGCCAGGGGTGA | 23607 |
rs745478844 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47496542 | ATCACAGATGTATGC[A/G]GTTATGTGGTGCTAT | 23607 |
rs745483252 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47488081 | TTTCTGTGTGGTTCA[C/T]TGAAGCTCTTAAGTC | 23607 |
rs745493163 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47542861 | TTTAATTTAGAAAGC[-/T]TATTTGTGGCTGGGC | 23607 |
rs745494152 | in-del | -/TTTG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47578041 | CACATAGTTACCTTT[-/TTTG]TTTGTTTTAGTGGCA | 23607 |
rs745497839 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47594197 | AAGTAGATAAAGGTG[G/T]TGGTTGCGTAACATC | 23607 |
rs745500591 | snp | C/T | 1.65411e-05 | 0.00287581 | intron-variant | CD2AP | GRCh38.p7 | 6:47577123 | GGTGTTTCTGTTTTT[C/T]AGTGAATTGCTTAAT | 23607 |
rs745524023 | in-del | -/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47517544 | ATATGCCTGCCTTGA[-/C]CTCCCAAAGTGCTGA | 23607 |
rs745528714 | snp | A/T | 1.65345e-05 | 0.00287524 | intron-variant | CD2AP | GRCh38.p7 | 6:47576995 | AGCCACATTATTTAC[A/T]TTCTTTATTTCAGCT | 23607 |
rs745540981 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47608720 | AGTGACTCTTCCTGG[A/G]CCTATTAAATTGTTC | 23607 |
rs745555788 | snp | C/T | 1.65839e-05 | 0.00287953 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47606256 | AAGAAGGTTGCCGGG[C/T]CGTTTCAATGGTGGA | 23607 |
rs745581298 | in-del | -/AG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47558274 | ATGTCATCTGCAAAC[-/AG]AGATAATTTTACTTC | 23607 |
rs745592031 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47539369 | TAGGACATACAAGCA[C/T]ATGGAGATTGGGAGA | 23607 |
rs745599031 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47555647 | AGACTGCTTATGTAC[C/T]GAATACTTGTCATTG | 23607 |
rs745655494 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47489816 | TTATATCTTAAAACA[G/T]TTTGAGAAGGAAGAT | 23607 |
rs745753573 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47533804 | TCAAAATAGAAGGAT[A/G]TTTTATAACTGTGTC | 23607 |
rs745775402 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47622423 | CCCTGTGGAGTTTTA[C/G]CCCCTGCTTCTCTGG | 23607 |
rs745815752 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47561842 | CTGGAGTGCAGTGGC[C/G]CGATCTTGGCTCACT | 23607 |
rs745830059 | snp | A/T | 1.64925e-05 | 0.00287158 | missense | CD2AP | GRCh38.p7 | 6:47554680 | GTGGAACCCTGAATA[A/T]CAAGTTGGGACTGTT | 23607 |
rs745847571 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47604574 | ATTGTACTTGTTAAG[A/G]TTTTTTCTTTGTGGG | 23607 |
rs745849008 | snp | G/T | 1.68309e-05 | 0.00290089 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624240 | TGAGTGGTGTGGACC[G/T]GGTGTTCATAATGTT | 23607 |
rs745866897 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47554179 | GGCTCTCAAAGTGCT[A/G]GGATTACAGACCTGA | 23607 |
rs745880014 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47563600 | CATTTGTGTACAGTA[C/T]TATGCTCTACCATAT | 23607 |
rs745881100 | in-del | -/TA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47547488 | AGTATCACAATTCTA[-/TA]TATATATATATGCAC | 23607 |
rs745947224 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47515377 | GAGATCAGAGTGCTA[C/T]ATTGAGAGTGGAAAT | 23607 |
rs745973584 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47614535 | GGGTGCCAGAACAAT[C/T]ACAATATTAACATCA | 23607 |
rs746053883 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47492780 | ATTTATTGATTTTAT[C/T]GATGTTTTCAAATAA | 23607 |
rs746072614 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47576175 | TGAACTCCTGGTTTC[A/T]TGCAGTTCTCCTGCC | 23607 |
rs746098698 | snp | C/T | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626695 | GTGTAACAGAAGATA[C/T]TCTTTTTTATGCTCC | 23607 |
rs746124377 | snp | A/G | 1.64792e-05 | 0.00287042 | missense | CD2AP | GRCh38.p7 | 6:47503360 | GAAATCATCAGGAAT[A/G]TGAAAAAGCTACAGG | 23607 |
rs746139125 | snp | G/T | 5.07533e-05 | 0.00503727 | intron-variant | CD2AP | GRCh38.p7 | 6:47608061 | CTAAGGTTTGTTGAC[G/T]TTCTGGGATTCTTTG | 23607 |
rs746139434 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47613210 | ACATTTTGACTTTCT[C/G]TTATGAATCGTGAAT | 23607 |
rs746169811 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47536255 | GTTACTGTTTGGATC[A/G]TATCTCTAATTCCCA | 23607 |
rs746199396 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47570479 | CTGTTTTGTCTCATT[A/G]TGGCACCTCCTGCAT | 23607 |
rs746211561 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47483289 | TCTATATGTGCCTAC[A/G]GTCAGCTTGTCAGCA | 23607 |
rs746217015 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47517285 | AGCCAATTAAACTTC[-/T]TTTTTTTTTTTTTTG | 23607 |
rs746258422 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47524187 | TAATACATTTTGTTT[C/T]GGCTAAGGTATTTCA | 23607 |
rs746283610 | snp | G/T | 1.67685e-05 | 0.00289551 | intron-variant | CD2AP | GRCh38.p7 | 6:47503234 | TATAGTTTACAGTAT[G/T]TTGTGAATTAGATTT | 23607 |
rs746283799 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47566144 | ATTCTCTCAGAAATC[A/G]CCTTATCAGTGAGGC | 23607 |
rs746288104 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47485081 | TAGCATGTACATACA[A/T]TTATATGTAGTACAT | 23607 |
rs746297717 | snp | A/G | 1.65485e-05 | 0.00287645 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47576538 | GCCCTTAATCCTACA[A/G]TCACTGGGACCCAAA | 23607 |
rs746317355 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47599473 | ACAGCGGTGGTGCAT[C/T]TAAAAAAAAAAATTG | 23607 |
rs746327167 | snp | A/G | 1.65693e-05 | 0.00287826 | intron-variant | CD2AP | GRCh38.p7 | 6:47574269 | GGTAATGATGGACTT[A/G]TTAGATTAACTCCAC | 23607 |
rs746327948 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497913 | CCGTTTAGTATAGAC[C/T]GTTTGTTCCTTAGAT | 23607 |
rs746335100 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47500864 | CCATTTCTCCTGCCT[C/T]AGCCTCCTGAGTAGC | 23607 |
rs746425906 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47535335 | TGTATAAATCCCTGT[A/G]GTACAAAATATTCTA | 23607 |
rs746452547 | snp | A/T | 1.78039e-05 | 0.00298356 | missense | CD2AP | GRCh38.p7 | 6:47612528 | AAGACAATGAGAAGT[A/T]ATCTAGAGGTAATTA | 23607 |
rs746460356 | snp | C/T | 1.65015e-05 | 0.00287237 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47595979 | TTCTGGAACAGTGTA[C/T]CCAAAGCGACCTGAA | 23607 |
rs746489910 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47593913 | GGGTAAACAGATTGT[G/T]TTTTATATATGTGTG | 23607 |
rs746499088 | in-del | -/TTAAAACACAATGAAGAAAATATA | 3.04562e-05 | 0.0039022 | intron-variant | CD2AP | GRCh38.p7 | 6:47554785 | ACTATTTTTTAAAAT[-/TTAAAACACAATGAAGAAAATATA]TTTTAATTGATTTAA | 23607 |
rs746512071 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47624100 | TGAAGGCTTGAAAGT[A/G]TGATCACATCTTAAT | 23607 |
rs746536725 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47496324 | GTTGTTGCTAAGTCA[C/G]CCATTAGTCTGAATG | 23607 |
rs746553554 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47546044 | AATTCAGAAGGTAAG[G/T]TATTTAGCTAATCAG | 23607 |
rs746575514 | in-del | -/AG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47589587 | ATATATATATTTGTC[-/AG]AGTCATCTGCTAGAA | 23607 |
rs746594734 | in-del | -/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47579608 | GGAGTTTCAGATGTA[-/G]CTATTCAGGTAGGAG | 23607 |
rs746596844 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47622785 | GCAGTCGGTCTGGAG[G/T]TAAAATACACAATGC | 23607 |
rs746618428 | in-del | -/GCTCCAGGTAT | 1.65026e-05 | 0.00287246 | intron-variant | CD2AP | GRCh38.p7 | 6:47580894 | CCACCTCCTGCTAAG[-/GCTCCAGGTAT]GTAAGAAGCATATTA | 23607 |
rs746647213 | snp | A/G | 1.79493e-05 | 0.00299572 | intron-variant | CD2AP | GRCh38.p7 | 6:47533786 | CTTTCCTGCATAATT[A/G]CATCAAAATAGAAGG | 23607 |
rs746656181 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47592778 | ACACCTGGAGAAGTT[A/T]CGGAAACTCTGCATC | 23607 |
rs746723496 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47559578 | AATTTTAGAGAAAAA[A/C]GTCAGATAATATTTT | 23607 |
rs746726128 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47552336 | CAAAGTCCAATGTAT[A/C]ATTCTTAAGCCTTTG | 23607 |
rs746737539 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47581008 | ATCAAGTATGATGTC[C/T]GTAAACATTTTTAGA | 23607 |
rs746747562 | in-del | -/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47540194 | AAAAAAAAAAAAAAA[-/G]AAAAAAGAAAAAATA | 23607 |
rs746747673 | snp | C/G/T | 3.32653e-05 | 0.0040782 | intron-variant | CD2AP | GRCh38.p7 | 6:47607906 | TCTATTATGTCTCTT[C/G/T]ACTTCTAAAAAATCA | 23607 |
rs746758621 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47481616 | CTCCCAAAGTGCTGG[C/G]ATTACAGGCGTGAGC | 23607 |
rs746777128 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47520019 | TTCTAACTTCTTAGG[A/G]CAAAACAAATTTTGT | 23607 |
rs746816454 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47504716 | TCAGTTCCAGACCAC[C/T]ACAATAGAGCAAATG | 23607 |
rs746834207 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47602919 | ATAAACAAAAAAAAA[A/G]CAATTTTAAAGAAAC | 23607 |
rs746837793 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47602621 | CCTGTGATCACAGCA[C/G]TTTAGGAGGCCAAAG | 23607 |
rs746853850 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47554021 | GAGTCCAGTGCCACA[A/G]TTGGGCTCAGCCTCC | 23607 |
rs746856409 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47578631 | CCTCTCCACCTTCCT[C/G]TCTTTTCCACTTCCT | 23607 |
rs746885327 | snp | A/G | | | downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47627731 | TAAAATTGGAAACAA[A/G]AAGAGCTAATCTCAG | 23607 |
rs746907053 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47479255 | TGCAGTTGAGAGTTG[A/G]TACTGCTTCATATCA | 23607 |
rs746924439 | in-del | -/AA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47549462 | TTTACAATAGCTGCA[-/AA]AAAAAAAAAAAAAAA | 23607 |
rs746941830 | snp | A/G | 3.32149e-05 | 0.00407509 | missense | CD2AP | GRCh38.p7 | 6:47606264 | TGCCGGGCCGTTTCA[A/G]TGGTGGACATTCTGT | 23607 |
rs746946152 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47616705 | TTTTCACTTGAGGTT[A/C]ATTTGTGAAATATGA | 23607 |
rs746967141 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47617410 | CTCTAAATCAAATTC[A/G]TATTTTCCCAGCTTG | 23607 |
rs746967799 | in-del | -/TGTGTGT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47491282 | GTGTATGTGTGTGTG[-/TGTGTGT]GTGTGTGTGTGTGTG | 23607 |
rs746969235 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47532125 | AAACAATCTGTAATA[C/G]TTTTATAATCATAAG | 23607 |
rs747003115 | in-del | -/TT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47601260 | ATAGTAAACAGAGAC[-/TT]TGTGGAACAGGGTGT | 23607 |
rs747014445 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47581930 | TTCAACTCATCTTTA[C/T]TTTTTAGAAGTGTAA | 23607 |
rs747014472 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47566871 | GTCTATCATTGATGG[A/G]CATTTAGGTTGGTTC | 23607 |
rs747044907 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47527170 | TTTTTGAACAGTTAC[A/G]TGAAGAGGTCATGTT | 23607 |
rs747054987 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47540423 | ATAGGCAGTCACCTC[A/T]ATTTATGAGTGAACC | 23607 |
rs747086788 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47526886 | GTTGAGGTTGTAACT[A/G]CTAGTCTTTTATGTA | 23607 |
rs747091671 | in-del | -/TA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47598541 | AAAGAAATTGTGGTA[-/TA]TATATATATACCATG | 23607 |
rs747093988 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47494724 | TTCTCCTAGGAGTTT[A/C]CCACTTTCATGCTAT | 23607 |
rs747102783 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47514395 | GCTAACTTAGCAGAT[A/G]TTACTACATTCTTAA | 23607 |
rs747110506 | snp | G/T | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626536 | TGTATAGTTCAGGTA[G/T]TCTTTGAGACACACA | 23607 |
rs747138668 | in-del | -/CT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497358 | TTCCCTCCCCTTCCC[-/CT]TCCCCTTCCCCTTCT | 23607 |
rs747152574 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47525788 | ATCTATAAGCAAAAC[C/T]AATCAGTATAGCACA | 23607 |
rs747174683 | snp | A/G | | | intron-variant, downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47604214 | TGTTATGCCACGTGT[A/G]CAGTGTAAATCCATT | 23607 |
rs747194140 | snp | A/G | 1.67382e-05 | 0.00289289 | intron-variant | CD2AP | GRCh38.p7 | 6:47595833 | TAATTTTGATTGTTA[A/G]TAACTTGTGAAATAT | 23607 |
rs747200381 | snp | C/T | 1.6504e-05 | 0.00287258 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47554699 | GTTGGGACTGTTTCC[C/T]TCAAATTTTGTGAAA | 23607 |
rs747237992 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47589460 | CACAAATATATATAC[A/T]TATATACACACACAT | 23607 |
rs747275271 | snp | A/G | 1.65296e-05 | 0.00287481 | missense | CD2AP | GRCh38.p7 | 6:47582026 | CCTGAACTGATAGCT[A/G]CAGAGAAGAAATATT | 23607 |
rs747276163 | snp | G/T | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624446 | TCTTAACTGTGCTGG[G/T]ATTGCAAACACTTTT | 23607 |
rs747281313 | in-del | -/TT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47504373 | ATTTCTTGAATAAAC[-/TT]GTGTTTATTTTAGTT | 23607 |
rs747307105 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47533935 | TTTAGTCATGTGCAA[C/T]CAATAACAAATCAAT | 23607 |
rs747328096 | in-del | -/AA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47484261 | CTGTACTCATTTTTG[-/AA]TCATAACCTTGGTTT | 23607 |
rs747333731 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47584013 | TTCCGTAATGATATA[A/T]GATGTTGAATATCTT | 23607 |
rs747341287 | in-del | -/TTTCCTTTCA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497321 | TTTCCTTTCCTTTCC[-/TTTCCTTTCA]TTTCCTTTCCTTTCC | 23607 |
rs747343157 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47500675 | TTTTCTGGTCTCAAG[A/T]GGTTATAGCAATTGT | 23607 |
rs747373439 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47499521 | TGGCTTCCATTATCC[C/T]TCAAATATTTACAGT | 23607 |
rs747398903 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47535215 | GTTCAAGGTCATTGC[C/G]AAGGTCTGATTGCAA | 23607 |
rs747442754 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47571791 | CAGAGATTTTATTGA[C/T]TACATGGGCAATTCA | 23607 |
rs747447021 | snp | A/C | 3.30437e-05 | 0.00406457 | intron-variant | CD2AP | GRCh38.p7 | 6:47533557 | GAGGATTTAATATAA[A/C]AAATATAACTTAACT | 23607 |
rs747447237 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47562156 | TTGCCTTGTTCGTTT[C/G]CTTTTTAGTATAAAA | 23607 |
rs747463684 | snp | A/G | 1.64838e-05 | 0.00287083 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47503401 | GCTGGAAGGAGAACT[A/G]AATGGGAGAAGAGGA | 23607 |
rs747471673 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47515233 | TTTAAGACTAAAAGC[A/G]TGGGTTAAAGTAGGG | 23607 |
rs747477894 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47502056 | CACATTTGGGGCTCT[A/G]CTGGGGAAGGGTCTG | 23607 |
rs747494409 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47569633 | TAGAAAAAGTTCATT[G/T]TCTTAGGAGGAGTCA | 23607 |
rs747496653 | snp | C/G | 1.65395e-05 | 0.00287567 | missense | CD2AP | GRCh38.p7 | 6:47576566 | AAAACTCAGAGTGTG[C/G]AGATAACAAAAACAG | 23607 |
rs747522110 | snp | A/G | 6.66245e-05 | 0.00577129 | intron-variant | CD2AP | GRCh38.p7 | 6:47576646 | GGGAATAGTAGAAAC[A/G]TACTCAAATGTATTA | 23607 |
rs747544003 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47596285 | ATGAGAACACTTAAC[A/G]TTCACTCTTAGCATT | 23607 |
rs747564886 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47598089 | CAGAAACTGGACTAA[C/G]TACATGAATAGACAG | 23607 |
rs747597366 | snp | A/C | 1.67739e-05 | 0.00289597 | missense | CD2AP | GRCh38.p7 | 6:47599347 | AAATTTGAAACTGAG[A/C]CAGTATCAAAACTAA | 23607 |
rs747633001 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47527846 | TTCTACCCAGAGTTA[C/T]ATGGGAGTTCAGAGT | 23607 |
rs747640618 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47557196 | TTTCTTGTAAATATG[A/T]TTAAGTTCTTTGTAG | 23607 |
rs747679448 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47524102 | AAGACATTATTATAT[A/G]TAAACCATGTTAATG | 23607 |
rs747751472 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47620707 | TTTTCATTTGTGCTG[C/T]CTGTGATTTCTTTCA | 23607 |
rs747775838 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47565209 | GTGAATTAATCATCT[A/G]TTCTGTTACTGAGTG | 23607 |
rs747777406 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47585551 | CAGCAGAAAGGAGGA[A/C]GCCAAACAGACCTCG | 23607 |
rs747779402 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47569013 | TTACTTGGGAGGTTA[A/G]GTAAAAGAGATCATT | 23607 |
rs747790781 | snp | C/T | 1.67801e-05 | 0.00289651 | missense | CD2AP | GRCh38.p7 | 6:47624223 | AAGCTGTCCTGTCTT[C/T]TTGAGTGGTGTGGAC | 23607 |
rs747796269 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47522569 | GTGAAGAGTTTCTTG[A/C]CCTTGATATAAAGTG | 23607 |
rs747832531 | snp | A/G | 1.65064e-05 | 0.00287279 | missense | CD2AP | GRCh38.p7 | 6:47544686 | CTGAAAGTGGGAGAT[A/G]TTATTGATATTAATG | 23607 |
rs747843484 | snp | A/G | 1.65184e-05 | 0.00287384 | intron-variant | CD2AP | GRCh38.p7 | 6:47580848 | TCAGCCGTTTCCACC[A/G]TTATTATTTTAACAG | 23607 |
rs747843692 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47617845 | GGTCCTAGCTATCTT[G/T]CTTTACTTGCTGATT | 23607 |
rs747845725 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47565318 | ATGTTTCGGTTTTGT[A/G]ATGTCTCCTTTTTAA | 23607 |
rs747850293 | snp | A/G | 1.88898e-05 | 0.0030732 | intron-variant | CD2AP | GRCh38.p7 | 6:47612562 | TCTTCCAGCATTGAG[A/G]GTTTAGTGAGCATAA | 23607 |
rs747864005 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47570309 | AGGAGGAGGGAGGGT[A/T]TAGGCTCGATAGACA | 23607 |
rs747883790 | snp | G/T | 1.94539e-05 | 0.00311875 | intron-variant | CD2AP | GRCh38.p7 | 6:47533806 | AAAATAGAAGGATAT[G/T]TTATAACTGTGTCTA | 23607 |
rs747885391 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47621898 | CAGTGGGCGGGGCCG[A/T]AGAACTCCCAAGATT | 23607 |
rs747917583 | in-del | -/TTTTTTTTGA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47489180 | TTTTTTTTTTTTTTT[-/TTTTTTTTGA]GAAGTCTCGCTCTTG | 23607 |
rs747917744 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47486952 | ACTATTCTCTAGGGA[A/T]TTTCTCATTCTTTGT | 23607 |
rs747933768 | in-del | -/T/TT | 0.0296767 | 0.118802 | intron-variant | CD2AP | GRCh38.p7 | 6:47609102 | AAATAAAATCAGAAA[-/T/TT]TTTTTTTTTTACGTT | 23607 |
rs747963787 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47616571 | GTTTCCAACATTATC[C/G]TCTATTGGCAACTTC | 23607 |
rs747968596 | in-del | -/TT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47597385 | CTGCATATGATGATG[-/TT]TTAGAAAAGCCAAGA | 23607 |
rs747984610 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47552268 | CAGTGCACACTGTAC[A/C]TAATGTGTAGTCTTT | 23607 |
rs747990674 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47479093 | GGCATTAAACTAACT[C/T]CCTCAATCCTTTAAA | 23607 |
rs748004606 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47518905 | GCCTCTGTTGTGGTA[-/T]TTTTTTAGAAAGAGA | 23607 |
rs748038105 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47579228 | TGGTCCCAGCCACTT[C/G]GGAGGCTGAGTTGGG | 23607 |
rs748066535 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47605849 | TGAGTTTTTTATGCT[A/T]CTACAGTTTGTGATA | 23607 |
rs748087292 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47544545 | AAACATGGCATGTAA[A/G]TATACTGTTTTTAAA | 23607 |
rs748114234 | in-del | -/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47546889 | GCCTCCTCAACAAAA[-/C]AATTATCAGCCAAGA | 23607 |
rs748134392 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47588001 | ATTCCCAGTCAGTGG[A/G]TGGATTTATTTACAT | 23607 |
rs748140951 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47529542 | GAAACCCTGAACTGG[A/T]ATAGGTGCATAAATA | 23607 |
rs748147507 | snp | C/T | 8.89403e-05 | 0.006668 | intron-variant | CD2AP | GRCh38.p7 | 6:47478272 | CTCGGGCGCTTCCCG[C/T]CGCCCGTCCGGACCT | 23607 |
rs748162243 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47553308 | GTGTGTAGTGCTGCT[A/G]AGTAAAATTTGACAG | 23607 |
rs748171531 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47572104 | AACCAAACATGTCTT[C/T]AGTTATTGCCTCATG | 23607 |
rs748193477 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47623063 | ATCGTCTCAATCCAA[A/C]TTGAAGACAGGCTTG | 23607 |
rs748212424 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47504375 | TTCTTGAATAAACTT[A/G]TGTTTATTTTAGTTG | 23607 |
rs748235155 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47486203 | ATAAATAAAAGTTTT[A/G]GTGCCTTGAGTAGTT | 23607 |
rs748240314 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47487375 | GAACTTATGCTTACA[A/G]CTTCATAGTTTAAAA | 23607 |
rs748246106 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47538809 | CTGAATATTTACATC[C/T]ATTTTTCAGACATGA | 23607 |
rs748286077 | in-del | -/TA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47491270 | TGATATGTGTGTGTG[-/TA]TGTGTGTGTGTGTGT | 23607 |
rs748292018 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47597120 | TGTTGGCTGTGCCAA[C/T]AGTCCTCATGCATGC | 23607 |
rs748303250 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47617353 | CACATTTTGAATTCA[C/T]CTATACTCATGAATC | 23607 |
rs748337562 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47600764 | AAATAGAATTTGATC[A/G]GTTCATATTGTTTTC | 23607 |
rs748340899 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47519762 | TATAAAATTAGTCAA[C/G]AAATTTTTTTGAATA | 23607 |
rs748368069 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47619010 | CAGTATTATAATGTT[C/G]ACTAAAAATGAACAA | 23607 |
rs748372531 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47566675 | TGTGTCCATGTATTC[C/T]CATTGTTCAACTCCC | 23607 |
rs748391288 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47562977 | ATGGCAAAGAATCTT[-/A]ACGCCCAGTATGTCA | 23607 |
rs748415089 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47587049 | GACACATGCATTCAG[A/C]GAGGGCCAGTTGAAT | 23607 |
rs748430248 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47552023 | CAAGATTTAAGGGGT[A/G]GGGAACAGAGACCAC | 23607 |
rs748448466 | snp | A/G | 1.66568e-05 | 0.00288585 | intron-variant | CD2AP | GRCh38.p7 | 6:47595854 | TGTGAAATATTTTAA[A/G]TCTTAGATGAAAAAT | 23607 |
rs748448514 | snp | C/T | 3.30158e-05 | 0.00406286 | intron-variant | CD2AP | GRCh38.p7 | 6:47609325 | TAGCCCTTCTTTTCT[C/T]CTGTGAGTACTACTT | 23607 |
rs748463603 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47562033 | CCTCTTAAAGTACTG[C/G]GATTACAGGCGTGAG | 23607 |
rs748488019 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47547868 | GAAATCAACTCCAAA[A/C]GGAGCCTTGAAAACC | 23607 |
rs748493962 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47612943 | GCCTCTGCTTTATCA[A/G]CTAAGTTTATATTTT | 23607 |
rs748527013 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497922 | ATAGACTGTTTGTTC[C/G]TTAGATTTGTTGCGC | 23607 |
rs748550427 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47596163 | AAATTGACATATACA[A/G]TTGTGTGTATTTATT | 23607 |
rs748602325 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47610012 | AATGAATGTGTTGGG[A/G]TAGGTGATCTCTAAA | 23607 |
rs748640676 | snp | G/T | 1.64882e-05 | 0.00287121 | missense | CD2AP | GRCh38.p7 | 6:47609247 | ATTCCCTGGATGAAC[G/T]TAGAGCCCAGATTAT | 23607 |
rs748668302 | snp | C/T | 2.10613e-05 | 0.00324503 | intron-variant | CD2AP | GRCh38.p7 | 6:47533575 | ATATAACTTAACTTG[C/T]CTCTTTATTTATTTT | 23607 |
rs748720974 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47485000 | TATAGTAGTGCAACG[C/T]GTTACTCACTGTGTT | 23607 |
rs748727749 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47608574 | CAGGGCATTTTTGTC[-/A]GCGTTTCCAATTTAT | 23607 |
rs748729460 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47561305 | GCCCTTAGTCCTAGG[A/C]AATCATAGATCTGGT | 23607 |
rs748729616 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47575783 | AGTAGACTGTAGCTA[C/T]AAGGAACATAAGATT | 23607 |
rs748741607 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47608614 | TTAATCTGATTCTCT[C/T]AGCTGTCAGCAGTCT | 23607 |
rs748751953 | snp | C/G | 1.65479e-05 | 0.0028764 | intron-variant | CD2AP | GRCh38.p7 | 6:47576982 | ATCCATTTGTGTGAG[C/G]CACATTATTTACATT | 23607 |
rs748779150 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47568649 | CTTGGGAGGCTGAGG[C/T]AGGAGATTCGCTTGA | 23607 |
rs748786989 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47481708 | TGCACTTCTATAATA[C/G]AGTGATTTCTTTATG | 23607 |
rs748807951 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47522432 | AACCTGTTACTGTTA[C/T]AATGTTTTTATTTTG | 23607 |
rs748808287 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47508340 | CATCTTGCACTATTA[C/T]GTTATAGAAATGGCT | 23607 |
rs748822203 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47535012 | ATGTTGCCTGAGCTG[C/T]TCTTGAACTCCCGGG | 23607 |
rs748831939 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47620678 | ATTCTACCCATCCAC[G/T]AGCGTGGGATGTGTT | 23607 |
rs748833793 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47604857 | GTATCTGTTTTAATG[A/C]ATCAGCTTAGTTGAT | 23607 |
rs748856071 | snp | A/G | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626775 | TGATAAACATTTTAT[A/G]CTTGCATTTAAACTT | 23607 |
rs748897256 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47499191 | TTTCCTAAAGAGTCC[C/T]GATTCCTTTTAGTAG | 23607 |
rs748906344 | in-del | -/TATA | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624726 | GTGTGTGTGTGTATA[-/TATA]TATATATATTTTTAC | 23607 |
rs748922522 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47582402 | TTGAAGACCCAGTTC[C/T]TACTTAAGCATGAAA | 23607 |
rs748924523 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47597910 | GTGCAGTGGGCCCCA[C/T]CCACCCAGGACAGTG | 23607 |
rs748941769 | snp | C/T | 1.67668e-05 | 0.00289537 | missense | CD2AP | GRCh38.p7 | 6:47599360 | AGCCAGTATCAAAAC[C/T]AAAGCTAGATTCTGA | 23607 |
rs748991283 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47619706 | GTAGAAGTGTTCCCT[C/G]ATCACCTCATCCATG | 23607 |
rs749000684 | snp | A/G | 1.67956e-05 | 0.00289784 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624230 | CCTGTCTTCTTGAGT[A/G]GTGTGGACCTGGTGT | 23607 |
rs749013110 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47492992 | CACTTCATGTGTAGT[G/T]CTGGTACCATAGAGT | 23607 |
rs749024760 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47622417 | CCTTCTCCCTGTGGA[A/G]TTTTACCCCCTGCTT | 23607 |
rs749069111 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47592377 | TGACCTTAAATATAA[C/G]AGTTAAAACTCTTAG | 23607 |
rs749097753 | snp | C/T | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476101 | TAGCTTATATTTTTG[C/T]CTCCTTTCATGAATC | 23607 |
rs749147182 | snp | G/T | 1.65551e-05 | 0.00287702 | intron-variant | CD2AP | GRCh38.p7 | 6:47581982 | GTCTTCTTAAAAAAG[G/T]ATTAATGTTTTTTCC | 23607 |
rs749172050 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47494593 | TATTTCGCAGTGGTT[A/C]CTTTTCTTTTCCTCC | 23607 |
rs749175405 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47606580 | CAACAGTTATTAAAA[C/T]TGAGCAGCAGATACT | 23607 |
rs749183321 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47509738 | TTGCCCTTTGCTGGC[A/C]GTGTGGTATTAGACA | 23607 |
rs749188414 | in-del | -/TA | 5.04045e-05 | 0.00501993 | intron-variant | CD2AP | GRCh38.p7 | 6:47609075 | AAAATCTTTCGAACG[-/TA]AATATAATATTAAAT | 23607 |
rs749215134 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47555750 | TGATGGCAGAAAACT[A/G]TGCCTTGGTTGTCTT | 23607 |
rs749237927 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47556843 | GGGTGTATACCCAGT[A/G]ATAGGATTGCTGGGT | 23607 |
rs749272191 | snp | C/T | 1.64988e-05 | 0.00287213 | missense | CD2AP | GRCh38.p7 | 6:47580877 | AGAAACCAAAGAAAC[C/T]ACCACCTCCTGCTAA | 23607 |
rs749298471 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47541287 | CACCACCACGCCCGG[C/T]TAATTTTTTTGTATT | 23607 |
rs749311740 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47517988 | AGTGAAGTTGAATAG[A/T]AAATGTCAGTTTATC | 23607 |
rs749326055 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47577474 | AGTGTTGTTTGTAAT[A/G]TAAACAGAAGAAAAA | 23607 |
rs749331777 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47502618 | CCTACCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 23607 |
rs749334649 | snp | A/G | | | utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47478091 | AGGAGAGCGCCGCGG[A/G]CGGATGGAGGCGACT | 23607 |
rs749370460 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47546634 | CAGAAAAACTTCCCC[A/G]GCCTTGCCAGAGACC | 23607 |
rs749432421 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47575336 | GTGCCCCTTCTAACT[C/T]TAAAGCTTAGGATTA | 23607 |
rs749459476 | snp | A/G | 1.71838e-05 | 0.00293114 | intron-variant | CD2AP | GRCh38.p7 | 6:47478282 | TCCCGCCGCCCGTCC[A/G]GACCTTCCAGACCCG | 23607 |
rs749489482 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47563838 | CTATTTCTTTTCTCT[C/T]TAACTTAGCAATAAA | 23607 |
rs749502021 | in-del | -/GTAT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47491269 | CTGATATGTGTGTGT[-/GTAT]GTGTGTGTGTGTGTG | 23607 |
rs749511546 | snp | A/G | 3.30691e-05 | 0.00406613 | missense | CD2AP | GRCh38.p7 | 6:47607942 | CCAACTCACAGCCCC[A/G]AAAAAATCTTGAAGT | 23607 |
rs749513875 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47506865 | AGAGCGGCTGTGGCA[C/G]TTTCTAAGATGAGAC | 23607 |
rs749530775 | snp | A/G | 1.71658e-05 | 0.00292961 | utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47478203 | CACTGGAGGAGGAGG[A/G]GGAGGAGCGGACGTC | 23607 |
rs749537591 | in-del | -/GTTTTTTT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47489164 | TACTGCACTCAACTA[-/GTTTTTTT]TTTTTTTTTTTTTTT | 23607 |
rs749542658 | snp | G/T | 1.65452e-05 | 0.00287616 | intron-variant | CD2AP | GRCh38.p7 | 6:47574254 | AAAACCAGAAAAGGT[G/T]GTAATGATGGACTTG | 23607 |
rs749567350 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47516753 | GTTTGCTTATGAAAA[C/G]TTAGAAAACAGGACA | 23607 |
rs749574949 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47599557 | GGATAAAGTTGAAAT[C/T]ACACAGTTGAAATTT | 23607 |
rs749575135 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47565157 | TGTAGGATAAAAGTT[C/T]TAAGAATGCCACCAT | 23607 |
rs749585548 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47589681 | CAGTAAAGTCTGGCA[C/T]TGGGGCTCATATTTC | 23607 |
rs749595621 | snp | A/G | 1.78969e-05 | 0.00299135 | intron-variant | CD2AP | GRCh38.p7 | 6:47599264 | AAAAAGTCGTGTTTC[A/G]TACTAGTGATTTTTG | 23607 |
rs749595817 | snp | A/G | 1.64863e-05 | 0.00287104 | missense | CD2AP | GRCh38.p7 | 6:47574165 | AAAATTCGAGGAATT[A/G]GATTTGGAGACATTT | 23607 |
rs749616791 | snp | C/G/T | 1.65855e-05 | 0.00287967 | intron-variant | CD2AP | GRCh38.p7 | 6:47574279 | GACTTGTTAGATTAA[C/G/T]TCCACTCATTCTCTC | 23607 |
rs749620105 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47487212 | GCAGATCAAAACAAT[A/T]TTTTTAATGATGAAA | 23607 |
rs749639056 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47524221 | TGGTCACTACTGTAG[-/A]AATAAGGTAAACCAG | 23607 |
rs749662554 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47525602 | ACAACATGAAGGAGT[A/G]GTTTGTGAATTTTGT | 23607 |
rs749681363 | in-del | -/GTTTAGTCACA | 1.72279e-05 | 0.0029349 | intron-variant | CD2AP | GRCh38.p7 | 6:47544756 | GGTAATTGATGCTAT[-/GTTTAGTCACA]GGATTTTAGAAAAAT | 23607 |
rs749768109 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47522896 | TTGAAAAATTAGCAA[C/T]ATGAAGAATAAGAGA | 23607 |
rs749787577 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47622275 | CTGCCTTCTAGCTGC[A/G]AAAGAAAAGGGCTTG | 23607 |
rs749803658 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47572210 | ACATCAAAATTTTAA[A/G]TAAGTACTAGGTATA | 23607 |
rs749814923 | snp | A/G | 5.31335e-05 | 0.00515402 | intron-variant | CD2AP | GRCh38.p7 | 6:47533780 | TAATTCCTTTCCTGC[A/G]TAATTACATCAAAAT | 23607 |
rs749831057 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47548432 | GTGAACTTTTTTCTG[C/T]ACATAAACTAGAAAA | 23607 |
rs749832966 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47563187 | TGATTTTCTGAGCGT[A/G]TGTAATCCCTATGTA | 23607 |
rs749839993 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47622918 | CAGTTTACAAGAAGT[A/G]TTGCTGATTATGCAT | 23607 |
rs749889734 | in-del | -/AC | | | intron-variant | CD2AP | GRCh38.p7 | 6:47525082 | CTTATATTAAAAAAA[-/AC]AAAAATACTTCAGGA | 23607 |
rs749900406 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47614218 | CCTTTGCAATCAAAA[C/T]TTGGCTGTTTGGGGC | 23607 |
rs749919584 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47543441 | TCAGTCTGCTAGGGC[-/T]TACCATAACAAAATA | 23607 |
rs749920606 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47548925 | AGTAAATATGATATG[C/T]CACATAAACAGAATT | 23607 |
rs749955608 | snp | C/T | 9.89136e-05 | 0.00703186 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47579414 | TGGCTGGTGGAGGGG[C/T]GAACTTAATGGTAAA | 23607 |
rs749977187 | in-del | -/ATGT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47491259 | TTCTTTCTTCCTGAT[-/ATGT]GTGTGTGTATGTGTG | 23607 |
rs749991918 | snp | A/G | 8.25743e-05 | 0.00642498 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47608004 | GCCATCTGAATTAAA[A/G]AAAGATACATGCTAC | 23607 |
rs750008026 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47491923 | TTCTTTTTAGGTAAG[A/G]ATTAAGTTCTTAGAG | 23607 |
rs750019442 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47515898 | AAGAAAGACACTTGA[C/T]GTAAAGGAAATTCAA | 23607 |
rs750021145 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47499071 | CACTTCTGTGGGTCA[G/T]TTTGATACCATTTCA | 23607 |
rs750028095 | snp | A/G | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626099 | ATCCCTGGTCATCCT[A/G]ATAATGGGATGAGGG | 23607 |
rs750068203 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47590326 | TAAATGAATTTGTTT[A/G]CATATATAAGTATAT | 23607 |
rs750068504 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47575505 | ACTGATCCAGGAATT[A/G]ATAAAATAGGGAGCA | 23607 |
rs750115756 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47593472 | TTTATAACAAGCATG[-/T]TTTATAAGCATGCTT | 23607 |
rs750137473 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47612806 | CTAAAAAAAATTGAA[A/C]CGATTGAACTCATAG | 23607 |
rs750144502 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47561862 | CTTGGCTCACTGCAA[C/T]CTCCGCCTCCCGGGT | 23607 |
rs750158112 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47576938 | ATACTTTACACAAGA[G/T]AGAGGCTAAATAAGT | 23607 |
rs750174965 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47569793 | TGCAGGCTAGTCACC[A/C]GGAGTCAAGGTATTA | 23607 |
rs750200080 | in-del | -/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47513159 | TTTTTTTTTTTTTTT[-/C]CTTCTTTTAAAGTAA | 23607 |
rs750208907 | snp | A/G | | | intron-variant, utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47522251 | CAGAGAAATATCAGC[A/G]GAATGATATCAAAAG | 23607 |
rs750212618 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47611584 | AAAATTCCTTCCTTA[C/T]GTATTTTTTCTTCAT | 23607 |
rs750221104 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47523469 | GTGTTGAATATGTTG[A/C]TTAAGCAAGAAATAA | 23607 |
rs750261596 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47481662 | CGTGGTGGTTTTAAT[A/G]GACAAATTTGTGGTT | 23607 |
rs750272900 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47556614 | TCGGCCTCCCAAAGT[A/G]CTGAGATTACAGGCG | 23607 |
rs750281156 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47564484 | CTTATGCTATTCAGC[C/T]TGATTTGGATTTTAG | 23607 |
rs750307379 | snp | A/T | 1.64762e-05 | 0.00287016 | missense | CD2AP | GRCh38.p7 | 6:47574118 | TGGGAAATGTGAGTG[A/T]AACTGCATCTGGATC | 23607 |
rs750314910 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47598554 | GTATATATATATACC[A/G]TGGAATACTACTCAG | 23607 |
rs750357577 | snp | A/G | 3.29837e-05 | 0.00406088 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47609293 | TGTAGAAGCACTGAA[A/G]AAGGATCACGGGTAA | 23607 |
rs750413618 | snp | C/T | 1.68074e-05 | 0.00289887 | intron-variant | CD2AP | GRCh38.p7 | 6:47595813 | TGGAAATAGAAAAAC[C/T]TAAATAATTTTGATT | 23607 |
rs750429637 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47524782 | AAGTTCCTTTGTCCA[A/G]AATGTGGAGAGCAAT | 23607 |
rs750430416 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47620538 | TATGCGGGCTCTTTT[C/T]TTGATTCCTAATGAA | 23607 |
rs750439122 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47494526 | TGGTATACAGCCCCT[C/G]ACAGTCTTTCCCTTG | 23607 |
rs750450204 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47578744 | TCACTGCAGCCTCTG[C/T]CTCCCGAGTTCAAGC | 23607 |
rs750450255 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47593210 | TCTTTTTAGACTATG[C/T]CACAAAAAGCATATT | 23607 |
rs750459384 | snp | A/G/T | 3.2998e-05 | 0.00406179 | missense | CD2AP | GRCh38.p7 | 6:47609217 | CTAAAGTGGAAACAG[A/G/T]TGATGTGAAAAAAAA | 23607 |
rs750482949 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47512198 | ATACAAAAAATTCGC[C/T]GGGAGTGGTGACATG | 23607 |
rs750486880 | in-del | -/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47515789 | CACTTTCAGATTTGA[-/C]CCTGGAAAAGGAAAA | 23607 |
rs750505426 | in-del | -/AG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47582232 | GTTCATTTCTCAAAC[-/AG]ATAACAATTTACATT | 23607 |
rs750531832 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47530297 | ATACAACCGTGAAAC[C/T]TCTGGCACAATAAAG | 23607 |
rs750545814 | snp | A/T | | | intron-variant, downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47604292 | CCAAAATGTGCACTG[A/T]TCCATTTTACTAACC | 23607 |
rs750557303 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47607440 | GTACGAGGGTTCCCT[A/G]TCTCCATATCCTTGC | 23607 |
rs750561307 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47510552 | GAGCTCCCAATATCT[A/G]GAGCTGGAACAGTTT | 23607 |
rs750572665 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47495605 | ATCTCGTCCGTGACT[C/G]TCTGGCTTTACCTGC | 23607 |
rs750599562 | snp | C/T | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476653 | ACCACATGTAACCTT[C/T]TGAGAAGCATTAGAA | 23607 |
rs750612328 | snp | C/T | 1.66394e-05 | 0.00288434 | intron-variant | CD2AP | GRCh38.p7 | 6:47576639 | TCATATTGGGAATAG[C/T]AGAAACATACTCAAA | 23607 |
rs750643366 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47591941 | GTGATTCTCTCACCT[C/T]GGCCTCCAGAGTAGC | 23607 |
rs750677587 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47538310 | ACAGTGCCATGATCT[C/T]GGCTCACTGCACCCT | 23607 |
rs750692695 | snp | C/T | 1.65562e-05 | 0.00287712 | missense | CD2AP | GRCh38.p7 | 6:47606216 | ACTTGCTTCATCTCA[C/T]TGCAAATAGACCAAA | 23607 |
rs750716552 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47567228 | CTATCTTTTCATGTA[C/T]GTTCAGCTCTTTGAG | 23607 |
rs750724689 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47542958 | GAGTTTGAGACCAGC[C/G]TGACTAACATGGTGA | 23607 |
rs750731903 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47529874 | GCTCGCCTTGCTATT[C/G]TTGAATTTTACCACC | 23607 |
rs750766027 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47502386 | GGGTCAAGCAGTGCT[C/G]CAAAGTAGCTGGGAC | 23607 |
rs750809565 | snp | C/G | 1.75557e-05 | 0.00296269 | intron-variant | CD2AP | GRCh38.p7 | 6:47599461 | AAGTCAGCATGGACA[C/G]CGGTGGTGCATTTAA | 23607 |
rs750814183 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47574834 | CTAAAAAGAGGCTTT[-/A]AAAATAAAACCTTAA | 23607 |
rs750819428 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47553034 | TGTTTGCTCCTAACA[C/G]CATTTTGTTCATATG | 23607 |
rs750854530 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47557831 | TTGGTTCCATATGAA[A/G]CATAAAGTAGTTTTT | 23607 |
rs750858924 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47531609 | TTTCCTGCAACAGCA[C/T]AACTCTCAAATTTTG | 23607 |
rs750861825 | in-del | -/TATTT/TATTTAC/TATTTACATGCC | 5.02107e-05 | 0.00501032 | intron-variant | CD2AP | GRCh38.p7 | 6:47544739 | ACAGGTAAAACAGTA[-/TATTT/TATTTAC/TATTTACATGCC]ATGGTAATTGATGCT | 23607 |
rs750874117 | snp | C/T | 1.65211e-05 | 0.00287407 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47577010 | ATTCTTTATTTCAGC[C/T]AAAGAATATTGTAGA | 23607 |
rs750907570 | snp | A/G | 0.000100801 | 0.00709863 | missense | CD2AP | GRCh38.p7 | 6:47599332 | TCTAGCATTTCATCA[A/G]AATTTGAAACTGAGC | 23607 |
rs750927016 | snp | A/G | 1.70345e-05 | 0.00291838 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624270 | TCCAGGGATTCAGAA[A/G]CAACGCTATGAACTT | 23607 |
rs750933489 | in-del | -/TATGTGTGTGTG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47491258 | TTTCTTTCTTCCTGA[-/TATGTGTGTGTG]TATGTGTGTGTGTGT | 23607 |
rs750946190 | snp | G/T | | | missense | CD2AP | GRCh38.p7 | 6:47554692 | ATAACAAGTTGGGAC[G/T]GTTTCCCTCAAATTT | 23607 |
rs750948195 | snp | G/T | 1.6495e-05 | 0.0028718 | intron-variant | CD2AP | GRCh38.p7 | 6:47554631 | TTTTTGCTTTTGAAT[G/T]GTGAACTTTTTCAGG | 23607 |
rs750949216 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47565956 | CCCATATCCCTCCCT[C/T]CACCTTTCTTACCTC | 23607 |
rs750973698 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47575388 | TAATGATTATATTAT[A/C]TTTTAATCATCCTTG | 23607 |
rs750989224 | snp | C/T | 1.67829e-05 | 0.00289675 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47624216 | CTGAAAAAAGCTGTC[C/T]TGTCTTCTTGAGTGG | 23607 |
rs750997072 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47486413 | TTAGTATGTGAATCC[A/G]TTAGAAAAATAAACG | 23607 |
rs750999759 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47611458 | TTTATTTCTTTACTT[G/T]GAGTTCAGAGGTTTT | 23607 |
rs751006057 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47526629 | ACATTGTTTTACAGC[A/C]AATGAACACAATGGA | 23607 |
rs751027325 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47591726 | TGCTATATTCTGAAG[A/C]AAATAAAAGGACATA | 23607 |
rs751033852 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47617077 | GGATCAAGTGATCCC[A/G]CCTCAGCCTCCCAAG | 23607 |
rs751035930 | snp | A/G | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625598 | ATTGTTTTATGCTTT[A/G]TTATATCGCAAATGA | 23607 |
rs751036941 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47513989 | ATCTTTTCACATTTC[A/G]GTTCCTTGTGTACAG | 23607 |
rs751042146 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497441 | ATCTGTTGCCCAGGC[C/T]GGAGTGCAGTGGTGC | 23607 |
rs751079762 | in-del | -/AAAAAAAAAA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47543149 | GAGCAAGACTGTCTC[-/AAAAAAAAAA]AAAAAAAAAAAAAAG | 23607 |
rs751092419 | snp | A/G | 0.000197889 | 0.00994512 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47544667 | AAATGAGGATGAACT[A/G]GAGCTGAAAGTGGGA | 23607 |
rs751121503 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47527278 | GTATACCTGTTGTTG[C/T]TGCTCTTGGTCTGTC | 23607 |
rs751132248 | snp | A/T | 1.66707e-05 | 0.00288705 | intron-variant | CD2AP | GRCh38.p7 | 6:47580944 | CTATTTTCCATTTTT[A/T]AAAATTCTAAAATGG | 23607 |
rs751171358 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47524854 | TTTCAAAGTAGGTCT[A/G]CTATATCTGTCATTT | 23607 |
rs751183220 | snp | A/C | 9.94085e-05 | 0.00704942 | intron-variant | CD2AP | GRCh38.p7 | 6:47609078 | ATCTTTCGAACGTAA[A/C]TATAATATTAAATAA | 23607 |
rs751228925 | in-del | -/TTG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47499735 | TAGGAGTTAAGAGTT[-/TTG]TTGTTGTTGTTGTTG | 23607 |
rs751236543 | snp | C/G | 1.6549e-05 | 0.0028765 | missense | CD2AP | GRCh38.p7 | 6:47608015 | TAAAAAAAGATACAT[C/G]CTACTCTCCAAAGGT | 23607 |
rs751240534 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47614426 | CAGATAATAAGGAAG[A/G]CCAAGTAGAGGGGGA | 23607 |
rs751278706 | snp | G/T | 4.97451e-05 | 0.00498699 | intron-variant | CD2AP | GRCh38.p7 | 6:47503272 | TTCGTTTTTTCCCCC[G/T]TTTTTAGTTGACTAT | 23607 |
rs751282341 | in-del | -/AGATTC | | | intron-variant | CD2AP | GRCh38.p7 | 6:47560594 | CGATTCCTCATGATT[-/AGATTC]AGATTATATTTTATT | 23607 |
rs751286070 | snp | C/G | 3.29516e-05 | 0.00405891 | missense | CD2AP | GRCh38.p7 | 6:47574105 | CCTATACCTTCTCTG[C/G]GAAATGTGAGTGAAA | 23607 |
rs751325628 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47534554 | TCTACTAAATATACA[A/G]ATTAGCCGGGCGTGG | 23607 |
rs751344316 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47583450 | CTTCAACCCTTGTCA[A/G]CCATTAATTTTTTTA | 23607 |
rs751365763 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47533399 | TCTTCATCTCCAGTT[C/G]TGATAAAACTTAAAC | 23607 |
rs751373090 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47541938 | ACTTCTTAGGATTCT[C/G]CTTTGTTGTCCTCTC | 23607 |
rs751384185 | snp | A/G | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520894 | TTCTTCTCTGCTTGC[A/G]TTGGCATTTCTATGT | 23607 |
rs751400702 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47619196 | GTATATACTGCACCA[C/T]GTTCGTAGTCTTTCA | 23607 |
rs751431869 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47595578 | CTACACTTAAAAGCA[A/G]AGCTTCCTGGGAACA | 23607 |
rs751432387 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47568455 | GGTATAAGAAACGAT[A/G]AGTAGGCTGGGCGCG | 23607 |
rs751438191 | snp | C/T | 1.71502e-05 | 0.00292827 | intron-variant | CD2AP | GRCh38.p7 | 6:47478259 | CATGGGTAAGAGACT[C/T]GGGCGCTTCCCGCCG | 23607 |
rs751471837 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47570528 | TTTTCCTTTCTCCTT[G/T]CTCCTTATCCTCTTT | 23607 |
rs751486978 | snp | G/T | 1.65479e-05 | 0.0028764 | intron-variant | CD2AP | GRCh38.p7 | 6:47596050 | TACCTAATTTTAAAT[G/T]AGCTTACTGATTTAC | 23607 |
rs751495353 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47514916 | AATTAGCCAGGAGTG[A/G]TGGCACGCACCTGCA | 23607 |
rs751530974 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47612566 | CCAGCATTGAGAGTT[C/T]AGTGAGCATAAACTG | 23607 |
rs751536166 | snp | C/T | 1.81572e-05 | 0.00301302 | intron-variant | CD2AP | GRCh38.p7 | 6:47612467 | TAATAAGTACTTTGT[C/T]TTTAGGAAAGAACTG | 23607 |
rs751571094 | in-del | -/G | 3.30115e-05 | 0.00406259 | intron-variant | CD2AP | GRCh38.p7 | 6:47533562 | TTAATATAAAAAATA[-/G]TAACTTAACTTGCCT | 23607 |
rs751585032 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47596879 | TACATTCCTACCAGC[A/G]GTGTGCAAGGGTTCC | 23607 |
rs751592398 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47590899 | TTGAGGCAAGGAATT[C/G]AAGAAGACACACAAA | 23607 |
rs751625179 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47558500 | GAGATATGTTCCATC[A/G]ATACCTAGTTTGTTG | 23607 |
rs751631917 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47578428 | TTGCCCAGGCTGGTG[-/T]TTGCAAACTCCTGGC | 23607 |
rs751640123 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47523282 | CAGATATTGGAATAT[C/T]AAATGGAAGACAAGT | 23607 |
rs751671676 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47509296 | ACTAATCACAGATCA[C/T]CATAACAGATATAAT | 23607 |
rs751673479 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47620302 | AATTATCCCAGCACC[A/G]TTTGTTGAAAGGGGT | 23607 |
rs751721973 | in-del | -/TAGAAGTATCCATT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47523899 | AAAGTCAAAGCAATA[-/TAGAAGTATCCATT]GTGAAAAGTACCTTT | 23607 |
rs751746319 | snp | A/C | 1.68252e-05 | 0.0029004 | missense | CD2AP | GRCh38.p7 | 6:47533749 | CAAACCAAAAACATT[A/C]AGAAGAGTATGTAAA | 23607 |
rs751749055 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47608200 | CTATTTTCTGCAAAT[A/G]TTTTTGAAAGAGCTT | 23607 |
rs751755830 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47510210 | TACAGGTAGATACAG[G/T]AATGGTTTTGTATAT | 23607 |
rs751757744 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47492617 | TACAGGTGTGAGCTA[C/T]TGTGCCTGGCCTCTG | 23607 |
rs751759223 | snp | C/T | 3.31148e-05 | 0.00406894 | missense | CD2AP | GRCh38.p7 | 6:47533677 | GGGAATGTAGCAAGT[C/T]TTGTACAACGAATAA | 23607 |
rs751804408 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47564701 | AATGCCAGGAAGTGA[A/G]CATTATATAAGGAGT | 23607 |
rs751842788 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47508472 | TTGCTCTAGATGAGG[A/C]TTTAGCTTAGGGAAA | 23607 |
rs751844168 | snp | C/G | | | missense | CD2AP | GRCh38.p7 | 6:47606179 | GATGTTGTAAATTTT[C/G]ATGACATAGCTTCCT | 23607 |
rs751886063 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47569618 | CTAGTCTCTTACAGG[C/T]AGAAAAAGTTCATTT | 23607 |
rs751911376 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47516202 | ACATCCTTTCATGCA[A/G]AGTTTGGTCCAGCTA | 23607 |
rs751941123 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47615674 | CTGGCCCCACCTCCA[A/G]CACTGGGGATTACTT | 23607 |
rs751963703 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47600466 | CTTCCCTCTTTCAGT[C/T]TGCGAATGCAAAGTT | 23607 |
rs751977603 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47565844 | ACTGAATAGTCTGGT[A/T]GCCAGTAGTGATCAC | 23607 |
rs751993865 | snp | C/T | 8.87823e-05 | 0.00666208 | intron-variant | CD2AP | GRCh38.p7 | 6:47478273 | TCGGGCGCTTCCCGC[C/T]GCCCGTCCGGACCTT | 23607 |
rs751994532 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47550302 | ATCTTCACAATCTAT[A/C]CATCTGACAAAGGAC | 23607 |
rs752009632 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47536545 | AAACTGGATTGGACT[-/A]GTGAGCTATTCTTCT | 23607 |
rs752027498 | snp | C/T | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476553 | ATGATGTCAATGTAA[C/T]CTTGTTTAGGTGAGT | 23607 |
rs752029188 | snp | G/T | 3.30158e-05 | 0.00406286 | missense | CD2AP | GRCh38.p7 | 6:47577063 | CTAATGAAGATGAAC[G/T]TACTTTTAAAGAGGG | 23607 |
rs752039980 | in-del | -/ATTGGTA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47480911 | GTGCGAAAGTCCATT[-/ATTGGTA]AGAGCTTTAGTTGCT | 23607 |
rs752045754 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47544142 | TGTCTGAAAATAGTT[A/C]TTAAAGAAGATAAAA | 23607 |
rs752058905 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47504673 | GTATTTTATTCTGCT[A/G]CAGGGGTACCTTGGA | 23607 |
rs752061300 | in-del | -/TA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47560801 | GAGATACTTTGAGAC[-/TA]TGTAAATATGCTATT | 23607 |
rs752068341 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47578461 | CAGGCAATCTTCCCA[C/T]ATCAGCCTCTGAAGT | 23607 |
rs752092981 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47587408 | GGGATATTTTCTCAA[A/G]TGTTTAGATAGGTGA | 23607 |
rs752102223 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47529117 | TCTTTCAGCGTTTCT[C/G]CCCTTTGTCACGATT | 23607 |
rs752139168 | snp | A/G | 3.70089e-05 | 0.00430152 | intron-variant | CD2AP | GRCh38.p7 | 6:47599469 | ATGGACAGCGGTGGT[A/G]CATTTAAAAAAAAAA | 23607 |
rs752168118 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47614108 | GCTATCTAGACCACT[C/G]AAACTTTCCTTCATA | 23607 |
rs752181019 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47622685 | GGGACACACACACTA[A/T]TTGGGGTGTTTCCCA | 23607 |
rs752209285 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47486844 | GGATTGTAAATGTAG[A/G]AGCTCATATACTGTA | 23607 |
rs752226385 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47484980 | GAGTTGTAGCCATCC[C/T]ACACTATAGTAGTGC | 23607 |
rs752247015 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47595212 | ATAGTATAAAATTGT[C/G]AAAATTGTTTTTTTC | 23607 |
rs752270166 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47538289 | TCTTCTTACCCAGGA[C/T]GGAGTACAGTGCCAT | 23607 |
rs752341623 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47529110 | TTCTGACTCTTTCAG[C/T]GTTTCTCCCCTTTGT | 23607 |
rs752350720 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47505910 | GGGGCTGACCCCCCC[A/C]ACCTCCCTCCCGGAC | 23607 |
rs752418218 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47618151 | TGGCAAAACCTTGTC[C/T]CTACTAAAAAATATA | 23607 |
rs752426428 | snp | C/T | 3.32154e-05 | 0.00407512 | intron-variant | CD2AP | GRCh38.p7 | 6:47581952 | GAAGTGTAATTGTCT[C/T]TGTGCTTTAAAACTG | 23607 |
rs752432210 | in-del | -/AAG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47609530 | AAAAAAAAAAAAAAA[-/AAG]AAAAGAAAAGAAAAG | 23607 |
rs752438038 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47551558 | GGTATTTTTATCCCC[A/G]TTGTACATAGGAAGA | 23607 |
rs752450386 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47547195 | GGAATGGTGTCTCAC[A/G]TGTCAATACTAATGT | 23607 |
rs752486441 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47561706 | TATATTTTCATCTCT[A/C]ATGATTTTATTTCTA | 23607 |
rs752492917 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47595243 | CAGCTTATTTTCTTC[G/T]ACTTCAAATGGAAAT | 23607 |
rs752518366 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47513768 | ATGTGTACAGCTGAA[A/G]ATTTGCTGACTCCTA | 23607 |
rs752519964 | snp | A/G | 1.65111e-05 | 0.0028732 | missense | CD2AP | GRCh38.p7 | 6:47503300 | TATATTGTGGAGTAT[A/G]ACTATGATGCTGTAC | 23607 |
rs752534715 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47545972 | TCCCCAAAAATCACA[C/G]TAGCTCACCAGCAAG | 23607 |
rs752536188 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47610298 | CAAAAGCCCAGTAGG[A/T]AAAATATATTTTAAA | 23607 |
rs752540357 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47512523 | TGCTGAATTGTTTTT[A/G]TGGCTTATTATGAAA | 23607 |
rs752559811 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497513 | ATTCTCTCACTCAAG[C/G]CATCCTCTCACTTCA | 23607 |
rs752562385 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47539111 | TTCAGAATTCACAGT[C/G]TAGCAGGGGCGAACA | 23607 |
rs752573156 | snp | A/G/T | 5.01805e-05 | 0.00500881 | intron-variant | CD2AP | GRCh38.p7 | 6:47608038 | CCAAAGGTGAGGTGC[A/G/T]TTGTGGTCTAAGGTT | 23607 |
rs752581251 | snp | C/T | 1.66081e-05 | 0.00288163 | intron-variant | CD2AP | GRCh38.p7 | 6:47576508 | AAATAGTTTATGCCA[C/T]TTTTTTCTATTCTAG | 23607 |
rs752620843 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47623446 | CCTAAATCTTACCAT[A/G]ACAAGTCCTGTGTCA | 23607 |
rs752741758 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47620183 | ATCTTCAAGAATTTT[C/T]ATAGTTTCAGGTCTT | 23607 |
rs752753839 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47623051 | ACAATGAAAGCTATC[A/G]TCTCAATCCAAATTG | 23607 |
rs752788586 | in-del | -/CTTTT | | | downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47627554 | ATACGGTATAGTATC[-/CTTTT]CTTTGGGGAGATGCT | 23607 |
rs752790605 | snp | A/G | | | intron-variant, utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47603897 | AGGTGGTGCACATTG[A/G]TTTTTCTTTGTAATT | 23607 |
rs752822484 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47533265 | AATATTTACTATCTG[G/T]CACTTTATAGAAAGT | 23607 |
rs752830445 | snp | A/G | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521787 | TTGGGAGGCTGAGGC[A/G]GGCAGGTCACCTGAG | 23607 |
rs752833969 | snp | C/T | 1.69882e-05 | 0.00291441 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47599304 | TTCTTATTTCAGGAT[C/T]AATGGGGAAGTTTCT | 23607 |
rs752847632 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47555062 | AGTAAAGATATATTT[A/G]TATGCATTTTTGGTC | 23607 |
rs752862389 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47498735 | TCTGTTCTTTTAGAA[A/G]CTTTACATCTCTTGA | 23607 |
rs752876460 | in-del | -/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47572009 | GTTTGTTTTCAGGGG[-/C]CTCTCTGGCACATAC | 23607 |
rs752880361 | snp | C/G | 1.65176e-05 | 0.00287376 | missense | CD2AP | GRCh38.p7 | 6:47574229 | CATCCAGTAGTGAAA[C/G]AGAAGAGAAAAAACC | 23607 |
rs752886928 | snp | C/T | 1.80282e-05 | 0.0030023 | intron-variant | CD2AP | GRCh38.p7 | 6:47599256 | AATTTAAAAAAAAGT[C/T]GTGTTTCATACTAGT | 23607 |
rs752888842 | snp | A/G | 3.57369e-05 | 0.00422696 | intron-variant | CD2AP | GRCh38.p7 | 6:47624166 | TTTTATGTTTGCTCA[A/G]TTTATGTTTTTTGTT | 23607 |
rs752889368 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47507630 | GTTTGTATTTTCAGT[A/C]GAGATGGGCTTTCAC | 23607 |
rs752894591 | in-del | -/TCCATACATTATTGGGG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47619087 | GATAACTAATTTTTT[-/TCCATACATTATTGGGG]TAGAGGTGGTATTTG | 23607 |
rs752899858 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47494073 | GGGTTCAGATGCTTG[C/T]TTTGTCTCTTTAGAC | 23607 |
rs752924587 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47567494 | TTGTTTGAAGCTTTT[C/T]TTTCCATTGGGAAAG | 23607 |
rs752936134 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47481505 | TGTGTGCCACCATGC[C/G]CAGCTAATTTTTGCA | 23607 |
rs752976931 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47618566 | GTACATGTTAAAAAT[A/G]TATCTTAAATTCGCA | 23607 |
rs752977793 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47492105 | ACTTTGACCGTTTTA[C/T]TTTAAGTTTAGAAAT | 23607 |
rs752979654 | snp | C/T | 1.65007e-05 | 0.00287229 | missense | CD2AP | GRCh38.p7 | 6:47544617 | TTAGAGACCAAGAAG[C/T]GTCAGTGTAAAGTTC | 23607 |
rs752988197 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47548022 | CTGGGATAGCAAAGG[C/G]AGTGCTAAGAGGAAA | 23607 |
rs752990081 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47527596 | ATGAATGAATTGATA[C/T]GCTAGCTTGAAGAGG | 23607 |
rs753026691 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47583258 | AGTGAGCCTTCCTAC[A/G]TTGACACTTCTTTAT | 23607 |
rs753035234 | in-del | -/TC | 1.66554e-05 | 0.00288573 | intron-variant | CD2AP | GRCh38.p7 | 6:47607899 | CTTTGGTCTATTATG[-/TC]TCTCTTGACTTCTAA | 23607 |
rs753043217 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47601864 | AAGTACACTGACTTT[C/G]CTGTTAATAAAAGGG | 23607 |
rs753046234 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47542046 | TGTCCCACCTTCTTG[C/T]ATCTTACTCATATTT | 23607 |
rs753064781 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47528922 | CTTAGGCATCTTTTG[A/C]AAATATTTTCTCCCA | 23607 |
rs753087021 | in-del | -/AT | 3.37484e-05 | 0.00410769 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624251 | GACCTGGTGTTCATA[-/AT]GTTCCAGGGATTCAG | 23607 |
rs753142296 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47584438 | TTTTTTTTTTTGGCA[-/T]TGTGAATGTCTAGTT | 23607 |
rs753142488 | in-del | -/GTAGCTTA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47511125 | GGACAGGGAAAAATA[-/GTAGCTTA]GTAGCTTTTAATGGA | 23607 |
rs753145254 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47563264 | AGTAAGTATGCTAAT[A/G]GTATAAAATGACTTG | 23607 |
rs753186776 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47488627 | CATTTCAAGTGCTCA[A/G]TATTTTTTGATTATA | 23607 |
rs753187729 | in-del | -/GT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47501667 | GTTGTGGTTGTTGGT[-/GT]GTGTGTGTGTGTGTG | 23607 |
rs753231427 | snp | A/G | 1.65658e-05 | 0.00287795 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47606247 | GATGCCTGGAAGAAG[A/G]TTGCCGGGCCGTTTC | 23607 |
rs753266958 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47508789 | ACCTCAGGTGATCTT[C/G]TTGCCTCAGCCTCCC | 23607 |
rs753276648 | snp | C/T | 1.73769e-05 | 0.00294757 | intron-variant | CD2AP | GRCh38.p7 | 6:47606329 | TAGCAAATGCAGAGT[C/T]CATTGGAAGATAGAG | 23607 |
rs753288248 | snp | A/G | 3.30224e-05 | 0.00406326 | intron-variant | CD2AP | GRCh38.p7 | 6:47577109 | GATAAGTAAGGTAAG[A/G]TGTTTCTGTTTTTCA | 23607 |
rs753352774 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47500546 | AACTACTTCATGTAA[C/T]GAATCTGAAGGTATT | 23607 |
rs753353836 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47494244 | ATTTGCTCTAGCTGT[-/A]GGTGCCAGGGGGTTC | 23607 |
rs753380875 | snp | A/G | 3.29522e-05 | 0.00405894 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47574104 | ACCTATACCTTCTCT[A/G]GGAAATGTGAGTGAA | 23607 |
rs753430827 | in-del | -/AGGGCAAGTCAG | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476877 | TCTGCCTGGATCCAA[-/AGGGCAAGTCAG]TTTCAGTGCTGGATG | 23607 |
rs753436039 | snp | A/G | 4.95356e-05 | 0.00497648 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47595910 | ACCAGCAGCTCCACA[A/G]GTCCCACCCAAGAAA | 23607 |
rs753475038 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47613959 | CTTAAACCACATGAA[C/G]CAGCCTCTGCTACCT | 23607 |
rs753477461 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47516021 | GATAACTTTGTAAAA[C/T]GCATTTAATCATTGT | 23607 |
rs753479690 | in-del | -/AGAA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47605112 | ATATAAATATCTGAC[-/AGAA]AGTATTATAAACATC | 23607 |
rs753555116 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47598777 | GAGGGGAGTGAAGGA[C/T]AAAAGACTGCACATT | 23607 |
rs753557958 | in-del | -/CA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47549460 | CTTTTACAATAGCTG[-/CA]AAAAAAAAAAAAAAA | 23607 |
rs753580188 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47549074 | TAATAAAAGCCGTCT[A/G]TGCAAAACCACAGCC | 23607 |
rs753598095 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47564521 | CGCAGAATTTTATCT[C/G]TTAGAAATACCCTTC | 23607 |
rs753605078 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47558933 | CTCTGGTAGAGTTCG[A/G]CTATGAATCCATCTA | 23607 |
rs753607515 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47510942 | GCTGGGCATGGTGGC[A/G]TGCGCCTGTAGTCCC | 23607 |
rs753612514 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47504341 | ACCTGCACAGAATGG[A/C]TACATAGTTAATATT | 23607 |
rs753639563 | in-del | -/TC | | | intron-variant | CD2AP | GRCh38.p7 | 6:47494335 | CTTTCTCAGATAGAA[-/TC]TGTATCTTGCAGCTT | 23607 |
rs753656651 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47608940 | ACAAAAACCACTAAT[G/T]ATTACAAATGTATTC | 23607 |
rs753711994 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47544457 | GGTAAAAAGCTAACC[A/G]GGGCTGATTGTGATT | 23607 |
rs753722626 | snp | C/T | 1.68046e-05 | 0.00289862 | intron-variant | CD2AP | GRCh38.p7 | 6:47582105 | AAAAGCAATTATTTC[C/T]TTTATTGTCATTTTA | 23607 |
rs753731061 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47523740 | GAAAATATATATAAG[C/G]ATTTACATTTGATAA | 23607 |
rs753751160 | snp | C/G | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521963 | GAGGTTGCAGTGAGC[C/G]GAGATCATGCCATTG | 23607 |
rs753766715 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47621809 | TCATCCATCTCTTCT[A/G]GGTTTTCTAGTTTAT | 23607 |
rs753767394 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47536980 | ACACGTGAGGCAATA[C/T]ATAGTGTTTGCTAAT | 23607 |
rs753784019 | snp | A/C | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520322 | CTTGGATCTAAATAT[A/C]AGCTTTATTTTCCTA | 23607 |
rs753793812 | snp | A/T | 1.65157e-05 | 0.0028736 | missense | CD2AP | GRCh38.p7 | 6:47609194 | CCTGACTCCATTAGA[A/T]ATCAAAGCTAAAGTG | 23607 |
rs753799824 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47582125 | TTGTCATTTTAAAGA[C/G]AATTATTTCTCCACA | 23607 |
rs753839743 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47547826 | ATTATATCAAGCACT[C/G]TCTCACACCACAGCG | 23607 |
rs753847051 | snp | A/C | 1.98912e-05 | 0.0031536 | intron-variant | CD2AP | GRCh38.p7 | 6:47609113 | AGAAATTTTTTTTTT[A/C]CGTTTTCAGCCATCT | 23607 |
rs753853767 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47566050 | AACATTCCTCTCTCA[C/T]AGCCTTTGTGCTTGT | 23607 |
rs753882355 | in-del | -/CTTAGTAG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47511129 | AGGGAAAAATAGTAG[-/CTTAGTAG]CTTTTAATGGAGAAA | 23607 |
rs753886962 | in-del | -/GA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47544110 | TATCTTCAAATAAAT[-/GA]GAGTTTCATTTTTAG | 23607 |
rs753948211 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47567328 | TTAAAAGTCAAAGCC[A/G]GCAAAGGGAAATTCT | 23607 |
rs753950755 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47602156 | TTTATGTGTATATAT[A/G]AACTATGTATATAAA | 23607 |
rs753953131 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47519450 | TACGGCCTTTGGAAT[C/G]AGGATGTGTAGACCT | 23607 |
rs753968348 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47533014 | GGACAAGTCTGAATA[A/C]CACCTGTTTTTGTAA | 23607 |
rs754036606 | snp | C/G | 1.6571e-05 | 0.0028784 | splice-acceptor-variant | CD2AP | GRCh38.p7 | 6:47576523 | TTTTTTTCTATTCTA[C/G]CCCTTAATCCTACAG | 23607 |
rs754084673 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47616838 | TGCCAAATTCAAGGT[C/G]TCTTCTTCAGTGCCT | 23607 |
rs754113892 | in-del | -/AAAAG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47534681 | TCTGCTCCAAAAAAC[-/AAAAG]AAACTGTTATTTAAA | 23607 |
rs754117514 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47507543 | CAAGCGATTCTCCTC[A/G]CCTCCCTAGTTCAAG | 23607 |
rs754152403 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47538608 | GCTTTAATAAAACCT[G/T]AAGATATTTTTTTCC | 23607 |
rs754169935 | in-del | -/AT/ATAT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47566311 | TTAGAATATATATAT[-/AT/ATAT]ATATATATATATACA | 23607 |
rs754200490 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47554790 | TTTTTTAAAATTTTT[A/G]ATTGATTTAAATAAA | 23607 |
rs754236387 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47525428 | GTAACCTGCCTGTTT[C/G]ATTTGAGAAATGAAA | 23607 |
rs754257349 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47488510 | GTATTCAGTATAAAA[A/C]GTTATTAATGAGATA | 23607 |
rs754307046 | in-del | -/AA | 0.000581237 | 0.0170376 | intron-variant | CD2AP | GRCh38.p7 | 6:47599475 | AGCGGTGGTGCATTT[-/AA]AAAAAAAAATTGTCA | 23607 |
rs754315814 | snp | A/G | | | intron-variant, downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47604129 | ATTTTATGTGTTCCT[A/G]GCAACGTGCAGATTG | 23607 |
rs754319192 | snp | C/T | 3.29788e-05 | 0.00406058 | missense | CD2AP | GRCh38.p7 | 6:47544647 | CTTTTTGAGTACATT[C/T]CACAAAATGAGGATG | 23607 |
rs754355534 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47577434 | TTCCACCTCATTCTA[-/T]TTTTTTCTCCTGTCT | 23607 |
rs754370307 | snp | C/T | 1.81004e-05 | 0.0030083 | intron-variant | CD2AP | GRCh38.p7 | 6:47579541 | AGAACATTTTGCCAC[C/T]ATTCTTTTGCAAACA | 23607 |
rs754388353 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47553139 | ACAGGGATTTCTCAT[A/T]TGCAAGTTTGAATCT | 23607 |
rs754425245 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47607134 | TTGCAAATGACAGGA[A/T]CTCATTCTTTTTTGT | 23607 |
rs754447602 | snp | G/T | 1.64936e-05 | 0.00287168 | intron-variant | CD2AP | GRCh38.p7 | 6:47554638 | TTTTGAATTGTGAAC[G/T]TTTTCAGGTAGAAGA | 23607 |
rs754448100 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47501667 | TGTTGTGGTTGTTGG[G/T]GTGTGTGTGTGTGTG | 23607 |
rs754460421 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47535956 | CACTTTCTCTTCTAA[C/T]AGGAAAGGATACAGT | 23607 |
rs754500835 | snp | A/G | 1.64955e-05 | 0.00287184 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47544673 | GGATGAACTGGAGCT[A/G]AAAGTGGGAGATATT | 23607 |
rs754500891 | snp | A/T | 6.66467e-05 | 0.00577225 | intron-variant | CD2AP | GRCh38.p7 | 6:47580945 | TATTTTCCATTTTTT[A/T]AAATTCTAAAATGGT | 23607 |
rs754503496 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47500892 | AGCTGGGACTACAGG[C/T]GCCTGCCACCACGCC | 23607 |
rs754526716 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47482967 | TTGGGTGAGAATTGG[A/G]TGGAGCTGCAGACCT | 23607 |
rs754532083 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47586358 | TAGCAAATAGAACCA[C/T]TAAAAATGTATAGAA | 23607 |
rs754573503 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47598814 | AGTGTGCACTGCTCG[A/G]GTGGTGGGTGCACCA | 23607 |
rs754589495 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47535168 | TCCCATTATTGGAAT[A/G]CTAAGAATGTAGGAG | 23607 |
rs754602500 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47621864 | CTTGAATGATCTTTT[C/G]TGTCATTCAAGGGAC | 23607 |
rs754632399 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47500581 | TTAAAGGTGGTTAAT[C/G]TAGCAGTTTGATGAA | 23607 |
rs754662756 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47614498 | CACATGACATTTATC[A/T]ATTAAGTTTGCTGTT | 23607 |
rs754667916 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47564534 | CTGTTAGAAATACCC[A/T]TCCTTCTTTGTTTAA | 23607 |
rs754684139 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47549862 | GGTATAAAAATAGGC[A/G]TATTGACCAATGGAA | 23607 |
rs754699461 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47494688 | CCCACAATAGTGTGG[G/T]GACTCCCCCATAGGA | 23607 |
rs754708249 | snp | A/C | 1.65614e-05 | 0.00287757 | missense | CD2AP | GRCh38.p7 | 6:47608018 | AAAAAGATACATGCT[A/C]CTCTCCAAAGGTGAG | 23607 |
rs754740806 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47605221 | TTTTGGCTGTGGTTA[A/G]TATTCTGAGTTTGGA | 23607 |
rs754755823 | in-del | -/CATAACCTTG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47484264 | TACTCATTTTTGAAT[-/CATAACCTTG]GTTTTAACCACAAAT | 23607 |
rs754760474 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47608251 | AAATATTACATATTT[C/T]ATATTTTTTAAGGCA | 23607 |
rs754766551 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47560998 | TTATGTATTTATCAG[C/T]GTGGGCTCATCAGAG | 23607 |
rs754780337 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47609053 | AATTGTTTTTCTTCT[C/T]GCTGTTAAAATCTTT | 23607 |
rs754783834 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47542107 | CCTTCCATATCTGCT[C/T]CAGTTCAAACCTGTC | 23607 |
rs754860303 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47593688 | GATGTGGAGAAATTG[C/G]ACTTTTATACATTAC | 23607 |
rs754866941 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47510716 | TAATTCTAAATACTT[-/A]ATTTCCTTTTCCGCA | 23607 |
rs754887917 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47559191 | TTTATCATTTTTTAT[C/G]CATGTCTATTTGATT | 23607 |
rs754913465 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47523772 | GTGTACTCGCATAGC[A/T]TATGTGTCTTTTTCC | 23607 |
rs754928025 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47525163 | ACTATTTTTTAAAAT[A/G]TAAGCCTAAAATTAG | 23607 |
rs754944790 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47622571 | TAAATTGAGTCAGAT[C/T]CAGGTGAAGTTGGAA | 23607 |
rs754944898 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47607808 | ATTAATAATAATGGG[A/T]TATCAGCAACAGTAG | 23607 |
rs754952433 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47530327 | GATGCAGAGGCTCTA[C/T]GTGTTTATCAAGAAC | 23607 |
rs754966889 | snp | A/G/T | 0.000131865 | 0.008119 | missense | CD2AP | GRCh38.p7 | 6:47574157 | AGCCAAAGAAAATTC[A/G/T]AGGAATTGGATTTGG | 23607 |
rs754966909 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47617222 | CTCCCACTTTGGCCT[C/G]CCAAAGTGGTAGGAT | 23607 |
rs755019996 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47601938 | TTTTTCCCTTAACTA[A/G]CAATGGAATGATTTA | 23607 |
rs755054021 | in-del | -/AG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47562908 | CTCTGTAAAATTGAC[-/AG]AGAGAGAAAACCCTA | 23607 |
rs755086710 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47551902 | AAGGTCGTCGGACTT[A/C]CTATATGGCAGTTCA | 23607 |
rs755092995 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47567347 | AAGGGAAATTCTAGA[C/T]ATAAATACAATTGTT | 23607 |
rs755113586 | in-del | -/TC | | | intron-variant | CD2AP | GRCh38.p7 | 6:47558744 | TTTTATTGAGGATTT[-/TC]GCATTGATGTTCATC | 23607 |
rs755126777 | in-del | -/AAATT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47618537 | TAATAAATTATTGAC[-/AAATT]AATGAAAGTGTACAT | 23607 |
rs755139160 | snp | A/G | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520595 | TTTTCTGGTAACCAT[A/G]CCTCTGGTGGGTGGT | 23607 |
rs755212218 | snp | A/G | 3.38742e-05 | 0.00411533 | missense | CD2AP | GRCh38.p7 | 6:47533753 | CCAAAAACATTAAGA[A/G]GAGTATGTAAATAAT | 23607 |
rs755248543 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47619040 | TGAACATACAAGTGC[-/T]TAAAAGAGAAACTCT | 23607 |
rs755252225 | snp | A/G | 1.64947e-05 | 0.00287177 | intron-variant | CD2AP | GRCh38.p7 | 6:47609308 | AAAGGATCACGGGTA[A/G]GTAGCCCTTCTTTTC | 23607 |
rs755280551 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47478808 | CTCGGGTTCTACCTA[A/G]GCAAGTGTGTTGGCA | 23607 |
rs755283213 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47539881 | TAAAGGTTACTTATG[A/G]TAAGAAAATACTAAT | 23607 |
rs755302778 | snp | A/G | 3.31055e-05 | 0.00406837 | missense | CD2AP | GRCh38.p7 | 6:47533680 | AATGTAGCAAGTCTT[A/G]TACAACGAATAAGCA | 23607 |
rs755307455 | snp | C/T | 1.64923e-05 | 0.00287156 | missense | CD2AP | GRCh38.p7 | 6:47609238 | TGAAAAAAAATTCCC[C/T]GGATGAACTTAGAGC | 23607 |
rs755314914 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47531798 | TCCTTTTCGGCCGGG[C/T]GTGGTGGCTCACGCT | 23607 |
rs755315195 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47624069 | GAAACTGGATTTTAG[C/G]TCTGGAAAAAAAGTC | 23607 |
rs755319227 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47546290 | AGGTTTTTGAATTAA[C/T]CCAATCCAACAAAGA | 23607 |
rs755367650 | snp | G/T | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626131 | AGTTTCCAGCAGATT[G/T]CAGGCTGTTCTTAAA | 23607 |
rs755394624 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47600494 | GTTTCTGACTTAAAG[G/T]GTGGCCTCCTTTCAG | 23607 |
rs755408892 | snp | A/T | 1.65045e-05 | 0.00287263 | missense | CD2AP | GRCh38.p7 | 6:47577090 | AGGGGGAGATAATCC[A/T]TTTGATAAGTAAGGT | 23607 |
rs755425767 | in-del | -/T | 6.76407e-05 | 0.00581513 | intron-variant | CD2AP | GRCh38.p7 | 6:47579500 | TCCAGTAAGCTTTTG[-/T]TTTTTCAATGATGAT | 23607 |
rs755455325 | in-del | -/AAAG | 8.56458e-05 | 0.00654336 | intron-variant | CD2AP | GRCh38.p7 | 6:47599491 | AAAAAAAAAATTGTC[-/AAAG]AAACTCTTTAAGAGA | 23607 |
rs755468925 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47553157 | CAAGTTTGAATCTTT[C/G]CCTAGTAGTTAACAC | 23607 |
rs755502888 | in-del | -/TTAA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47584038 | TATCTTCTCATATGC[-/TTAA]TTGTCATTTGTATAT | 23607 |
rs755526304 | in-del | -/AA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47598960 | ACAGGAGCATTCTGT[-/AA]ACATTTTGATTTAGC | 23607 |
rs755553529 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47507570 | CAAGCGATTCTCCTT[G/T]CCTCCCCTTGGATTA | 23607 |
rs755587141 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47597539 | GGAGATTGAACATCT[A/T]AGTGAATAGTGTTCA | 23607 |
rs755595578 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47543096 | GTGGAGGTTGCAGCG[A/G]GCTGAGATTGCGCCA | 23607 |
rs755612631 | snp | C/T | 1.66785e-05 | 0.00288773 | intron-variant | CD2AP | GRCh38.p7 | 6:47576649 | AATAGTAGAAACATA[C/T]TCAAATGTATTAAGA | 23607 |
rs755634155 | in-del | -/GTTTTTTTT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47489164 | TACTGCACTCAACTA[-/GTTTTTTTT]TTTTTTTTTTTTTTT | 23607 |
rs755661268 | in-del | -/TG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47548659 | CAATCCTGTTGACAC[-/TG]TTTCACAAGATAGAG | 23607 |
rs755668250 | snp | C/T | 0.00016759 | 0.00915243 | intron-variant | CD2AP | GRCh38.p7 | 6:47599470 | TGGACAGCGGTGGTG[C/T]ATTTAAAAAAAAAAA | 23607 |
rs755681898 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47481690 | GTTGGTTTAGATGAT[A/G]TATGCACTTCTATAA | 23607 |
rs755686479 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47527531 | TTTCCTGAAGGAGGT[A/G]AGTTTCATATAAAGT | 23607 |
rs755733034 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47547758 | GTTCTTTCTCCAAGA[C/T]AGACCATATGATAGG | 23607 |
rs755743309 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47501427 | ACCTGATTGTACTTA[C/G]TGTCTGAGAAGTACA | 23607 |
rs755744394 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47612859 | TACCAGAGGGTGGGA[C/T]GGATATTAGTGGAAT | 23607 |
rs755750535 | snp | G/T | 4.05211e-05 | 0.00450099 | intron-variant | CD2AP | GRCh38.p7 | 6:47554792 | TTTTAAAATTTTTAA[G/T]TGATTTAAATAAACT | 23607 |
rs755800457 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47563205 | TAATCCCTATGTAGT[C/T]CAGAGGTGCAAGTAT | 23607 |
rs755808970 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47509532 | TCAGAGGTGAAGTAA[C/G]TACACTTTATATTTT | 23607 |
rs755818923 | snp | A/T | 3.3168e-05 | 0.00407221 | intron-variant | CD2AP | GRCh38.p7 | 6:47581968 | TGTGCTTTAAAACTG[A/T]CTTCTTAAAAAAGTA | 23607 |
rs755821785 | snp | G/T | | | missense | CD2AP | GRCh38.p7 | 6:47577021 | CAGCTAAAGAATATT[G/T]TAGAACATTATTTGC | 23607 |
rs755868413 | snp | A/T | 2.32194e-05 | 0.00340722 | intron-variant | CD2AP | GRCh38.p7 | 6:47609105 | ATAAAATCAGAAATT[A/T]TTTTTTTACGTTTTC | 23607 |
rs755899420 | in-del | -/AA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47609513 | AAACCCCATCTTTGC[-/AA]AAAAAAAAAAAAAAA | 23607 |
rs755909514 | snp | C/T | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520219 | ACATCTCTGGGGCCT[C/T]GTTATTAAAAGCTGA | 23607 |
rs755926689 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47621607 | CTTGTGGAATAGTGT[C/G]GAAAGGATTGGTACC | 23607 |
rs755941979 | snp | A/G | 4.95054e-05 | 0.00497496 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47580866 | ATTATTTTAACAGAA[A/G]CCAAAGAAACCACCA | 23607 |
rs755966329 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47510570 | GCTGGAACAGTTTGA[A/G]CAGCACAATAATCTA | 23607 |
rs756010304 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47556629 | GCTGAGATTACAGGC[A/G]GGAGCCACTGTGCCC | 23607 |
rs756011512 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47568568 | CACAAGTTGAAACCC[C/T]GTCTCTACTAAAAAA | 23607 |
rs756023991 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47569843 | TGTAATCATATATTA[A/G]TATTCACCTTATACT | 23607 |
rs756027160 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47534734 | GTGTACAAAGAATTA[C/T]GGTGTTATGGGAGCA | 23607 |
rs756083477 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47500738 | GTCTGCAGGAGGCCA[-/T]TCCTTCCTTGGTTTT | 23607 |
rs756095285 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47620656 | TATGGTCATTTTCAC[A/T]ATATTGATTCTACCC | 23607 |
rs756106744 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47535806 | GAATTTTTAGGCCCA[C/T]GGGAGGTTTTTTCAT | 23607 |
rs756107239 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47608494 | AACATAGTTTCACTA[C/T]AACTGAGACATAGAT | 23607 |
rs756113096 | snp | A/G | | | intron-variant, splice-donor-variant | CD2AP | GRCh38.p7 | 6:47522272 | ATATCAAAAGAGAAG[A/G]TTAACAAAGTATTTT | 23607 |
rs756142983 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47495664 | TGCTCTGTGTCCTCA[A/G]TTTTCTAATGGGTCC | 23607 |
rs756161725 | snp | A/C | 3.30666e-05 | 0.00406598 | missense | CD2AP | GRCh38.p7 | 6:47574243 | ACAGAAGAGAAAAAA[A/C]CAGAAAAGGTGGTAA | 23607 |
rs756196985 | snp | A/G | 1.69349e-05 | 0.00290984 | missense | CD2AP | GRCh38.p7 | 6:47599308 | TATTTCAGGATTAAT[A/G]GGGAAGTTTCTAGCA | 23607 |
rs756230664 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47599199 | TACAGAACAGAAAGT[A/G]ATCGGTATTAGGCCA | 23607 |
rs756231638 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47580210 | TAGTTTTACTAAAGA[A/C]TACGTTTTTCTGCTT | 23607 |
rs756247977 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47533441 | TGTTACCAAAATGTG[G/T]TTTATTCTTCAGATA | 23607 |
rs756250326 | snp | A/G | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476711 | ATAGGAAATAGTGGT[A/G]ATGGATACGTCCAAG | 23607 |
rs756318950 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47593525 | TGTTTAACATCATTA[A/G]TCATGTCAGTAAGCA | 23607 |
rs756353146 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47622415 | TTCCTTCTCCCTGTG[C/G]AGTTTTACCCCCTGC | 23607 |
rs756358015 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47578745 | CACTGCAGCCTCTGC[C/T]TCCCGAGTTCAAGCA | 23607 |
rs756389359 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47558869 | GAGTCCTTTTTTTGT[C/T]GTTGTTTGGAATAGT | 23607 |
rs756393733 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47543019 | AGCTGGGCGTGGTGG[C/T]GCTCACCTGTAATCC | 23607 |
rs756397117 | snp | A/G | 3.59868e-05 | 0.00424171 | intron-variant | CD2AP | GRCh38.p7 | 6:47599257 | ATTTAAAAAAAAGTC[A/G]TGTTTCATACTAGTG | 23607 |
rs756403090 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47504135 | AAATTCTCAGTAGTT[C/T]AGAGAAGAAGAAAAA | 23607 |
rs756405814 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47544277 | AGCCTAGAGGACTTG[C/T]CTATGATGAATTTGT | 23607 |
rs756406508 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47494545 | GTCTTTCCCTTGGAG[C/T]GTAGGCCTTTGTTAC | 23607 |
rs756411604 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47485277 | ATGACAGCCCTATGC[A/G]CGTTTTTCACCAGTG | 23607 |
rs756448414 | snp | A/G | 1.64857e-05 | 0.00287099 | missense | CD2AP | GRCh38.p7 | 6:47595948 | CACCTACCAAAGCCA[A/G]TAATTTACTGAGATC | 23607 |
rs756452107 | snp | A/G | 0.000139363 | 0.00834638 | missense | CD2AP | GRCh38.p7 | 6:47612493 | AACTGGAAAAACTGC[A/G]AAAAGATTTGGAAGA | 23607 |
rs756464734 | in-del | -/GTGTGTAT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47491265 | CTTCCTGATATGTGT[-/GTGTGTAT]GTGTGTGTGTGTGTG | 23607 |
rs756491832 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47550322 | TGACAAAGGACTACT[A/G]TCCAGAATCTACAAT | 23607 |
rs756493054 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47486923 | CATTTAAAGTTGGTC[C/T]TTTAAATGTATATAC | 23607 |
rs756508206 | in-del | ACTAAAAATAAAATA/GTCTCTACT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47585127 | TGAAACCCCGTCTCT[ACTAAAAATAAAATA/GTCTCTACT]AAAAAAAAAAAACCA | 23607 |
rs756511974 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47601662 | CCTAGTATTAGTAAT[A/G]TAAAAGTGTTCTACC | 23607 |
rs756568913 | in-del | -/AAC | 1.87929e-05 | 0.00306531 | intron-variant | CD2AP | GRCh38.p7 | 6:47579345 | TCTTAAAAAAAAAAA[-/AAC]AAAGGTCTATTGTCT | 23607 |
rs756572675 | in-del | -/TGTGTGTGTA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47491262 | TTTCTTCCTGATATG[-/TGTGTGTGTA]TGTGTGTGTGTGTGT | 23607 |
rs756609407 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47566026 | CTTAGGTTTCTTAAG[A/G]ATGTTAGGAACATTC | 23607 |
rs756624992 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47617100 | CTCCCAAGTAGCTGA[G/T]ACTACAGGCATGCAC | 23607 |
rs756632360 | in-del | -/TAGCTTAG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47511126 | GACAGGGAAAAATAG[-/TAGCTTAG]TAGCTTTTAATGGAG | 23607 |
rs756656266 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47551817 | AACCTTGAAGACTGT[A/C]ACTGCCAATTGGAGA | 23607 |
rs756669897 | snp | C/G | 1.66774e-05 | 0.00288763 | intron-variant | CD2AP | GRCh38.p7 | 6:47607890 | CTTTTCTTTTCTTTG[C/G]TCTATTATGTCTCTT | 23607 |
rs756675361 | snp | C/T | 1.74686e-05 | 0.00295534 | intron-variant | CD2AP | GRCh38.p7 | 6:47533772 | TATGTAAATAATTCC[C/T]TTCCTGCATAATTAC | 23607 |
rs756689277 | snp | A/G | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520628 | TTGGGGGCGAAAGTG[A/G]GGTCTATGGTGGTGA | 23607 |
rs756749683 | in-del | -/ACAT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47619313 | CACATGTCCATGAGA[-/ACAT]ACATACAATGTTTGA | 23607 |
rs756770392 | snp | A/G | | | missense | CD2AP | GRCh38.p7 | 6:47612526 | AGAAGACAATGAGAA[A/G]TAATCTAGAGGTAAT | 23607 |
rs756777784 | snp | C/G/T | 6.60582e-05 | 0.00574677 | intron-variant | CD2AP | GRCh38.p7 | 6:47577114 | GTAAGGTAAGGTGTT[C/G/T]CTGTTTTTCAGTGAA | 23607 |
rs756790635 | snp | A/G | 3.29979e-05 | 0.00406175 | missense | CD2AP | GRCh38.p7 | 6:47574205 | GCTCTGTGAAACTTC[A/G]GACAAGAACATCCAG | 23607 |
rs756799352 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47546046 | TTCAGAAGGTAAGTT[A/G]TTTAGCTAATCAGGG | 23607 |
rs756832328 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47561827 | GCTCTGTCACACAGG[C/G]TGGAGTGCAGTGGCG | 23607 |
rs756867778 | in-del | -/CAGTGCTGGATGACTGAGAA | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476892 | AGGGCAAGTCAGTTT[-/CAGTGCTGGATGACTGAGAA]TTACAAAATTTCTTG | 23607 |
rs756877107 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47623713 | ATACTGGTTACAGAT[A/T]AGTAAATTGAAACCA | 23607 |
rs756943306 | in-del | -/A | 1.66163e-05 | 0.00288234 | intron-variant | CD2AP | GRCh38.p7 | 6:47607912 | TGTCTCTTGACTTCT[-/A]AAAAAATCATTTAGC | 23607 |
rs756951561 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47525509 | GTCTATGGAATACAA[G/T]TAAATTGCTTTCTAT | 23607 |
rs756953001 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47575445 | ATTAGTGACTGTAGT[C/G]TCAGGGTTACCCTAT | 23607 |
rs756954027 | snp | A/G | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520898 | TCTCTGCTTGCATTG[A/G]CATTTCTATGTTGCA | 23607 |
rs756960248 | snp | A/C | 6.28674e-05 | 0.00560622 | intron-variant | CD2AP | GRCh38.p7 | 6:47554810 | ATTTAAATAAACTTT[A/C]TATAGCATCTAGTGT | 23607 |
rs756988829 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47481625 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCACC | 23607 |
rs757080622 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47596923 | GCTCACCAACACTTA[C/T]TATCTTTTATCTTTT | 23607 |
rs757088308 | snp | C/T | 1.64914e-05 | 0.00287149 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47554673 | TGGTGGAGTGGAACC[C/T]TGAATAACAAGTTGG | 23607 |
rs757121430 | in-del | -/TG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47556786 | GCTGCATTAAACATA[-/TG]TGTGTGTGTGTCTTT | 23607 |
rs757131000 | snp | A/G | 1.6804e-05 | 0.00289858 | intron-variant | CD2AP | GRCh38.p7 | 6:47595811 | TTTGGAAATAGAAAA[A/G]CCTAAATAATTTTGA | 23607 |
rs757191211 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47498943 | GAAATTAACATTGAT[C/T]TGTAATCTGTATGGA | 23607 |
rs757239773 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47490703 | GATATCTGTCACTTA[C/T]TCTAATTTAGTAACA | 23607 |
rs757310792 | in-del | -/TA | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624722 | GTGTGTGTGTGTGTG[-/TA]TATATATATATATAT | 23607 |
rs757326814 | snp | C/G | 3.30278e-05 | 0.0040636 | missense | CD2AP | GRCh38.p7 | 6:47609197 | GACTCCATTAGAAAT[C/G]AAAGCTAAAGTGGAA | 23607 |
rs757340925 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47492632 | CTGTGCCTGGCCTCT[G/T]TGTGTACATTCTTGT | 23607 |
rs757381028 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47591812 | AAATTATATACCTGA[A/G]ATAACTCTTTTCTGT | 23607 |
rs757387681 | snp | C/T | 3.91221e-05 | 0.00442261 | intron-variant | CD2AP | GRCh38.p7 | 6:47609114 | GAAATTTTTTTTTTA[C/T]GTTTTCAGCCATCTG | 23607 |
rs757394371 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47507928 | CAAAAGAATCTTTCT[A/G]CAGTAGGTCTCAACA | 23607 |
rs757417657 | in-del | -/TT | 6.89727e-05 | 0.0058721 | intron-variant | CD2AP | GRCh38.p7 | 6:47533567 | TATAAAAAATATAAC[-/TT]AACTTGCCTCTTTAT | 23607 |
rs757448238 | in-del | -/T | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520732 | GACTGGTGCTACAGT[-/T]TTTTTTTTTTTTTTT | 23607 |
rs757454906 | snp | A/G/T | 3.32437e-05 | 0.00407688 | intron-variant | CD2AP | GRCh38.p7 | 6:47576631 | TAAAGCTTTCATATT[A/G/T]GGAATAGTAGAAACA | 23607 |
rs757504005 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47590902 | AGGCAAGGAATTGAA[A/G]AAGACACACAAAAAA | 23607 |
rs757507978 | snp | C/T | 6.6268e-05 | 0.00575583 | missense | CD2AP | GRCh38.p7 | 6:47576524 | TTTTTTCTATTCTAG[C/T]CCTTAATCCTACAGT | 23607 |
rs757515446 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47540467 | AAATAATGTGGAATT[A/G]TTTTTTTCTTTTTAA | 23607 |
rs757533709 | in-del | -/ATT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47573861 | TTAAATTTACCTAAA[-/ATT]ATTATCGTTTTGCAC | 23607 |
rs757547693 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47569642 | TTCATTTTCTTAGGA[C/G]GAGTCAGCTGAAGTT | 23607 |
rs757558915 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47509298 | TAATCACAGATCACC[A/G]TAACAGATATAATGA | 23607 |
rs757566642 | snp | A/C/T | 8.93941e-05 | 0.00668506 | intron-variant | CD2AP | GRCh38.p7 | 6:47599265 | AAAAGTCGTGTTTCA[A/C/T]ACTAGTGATTTTTGC | 23607 |
rs757591994 | snp | A/G | 3.36751e-05 | 0.00410322 | missense | CD2AP | GRCh38.p7 | 6:47599321 | ATGGGGAAGTTTCTA[A/G]CATTTCATCAAAATT | 23607 |
rs757639761 | in-del | -/TATATATA | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624722 | GTGTGTGTGTGTGTG[-/TATATATA]TATATATATTTTTAC | 23607 |
rs757653488 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47502204 | CTATAGGTTGGCTTA[C/G]AGCATAGCAGCTTGT | 23607 |
rs757656409 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47550352 | TGAACTCCAACAAAT[A/T]AGCAAGAAAAAAACA | 23607 |
rs757687197 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47515052 | GTGAGAGTCCGTCTT[-/A]AAAAAAAAAAAAAAA | 23607 |
rs757748915 | snp | A/G | 3.29821e-05 | 0.00406078 | missense | CD2AP | GRCh38.p7 | 6:47544662 | CCACAAAATGAGGAT[A/G]AACTGGAGCTGAAAG | 23607 |
rs757758775 | snp | A/G | 1.76381e-05 | 0.00296963 | missense | CD2AP | GRCh38.p7 | 6:47612519 | GAAGAAGAGAAGACA[A/G]TGAGAAGTAATCTAG | 23607 |
rs757780070 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47578506 | AGCATGAACCACTGT[A/G]CCTGGTCAAATCGTG | 23607 |
rs757797991 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47564798 | CAATCTTTTCAGTCA[A/G]TAAAATAATTATGTT | 23607 |
rs757803894 | snp | A/G | 1.66596e-05 | 0.00288609 | intron-variant | CD2AP | GRCh38.p7 | 6:47580823 | TTAACTATATTTGAT[A/G]TGAAACTGGTCAGCC | 23607 |
rs757831426 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47516256 | ATGTGGCGGCACAAC[C/T]TTCTGGGCTGCTTTA | 23607 |
rs757839815 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47495351 | ACGTAAGCAAAGGAA[C/T]ACTAAAAATTGCTGG | 23607 |
rs757851261 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47530101 | CTGAGAAGTCATCCC[A/G]ATTTGCCTTAACACC | 23607 |
rs757853019 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47587433 | AGGTGATTAAACTCT[C/T]ACTTTCTACTTTCTG | 23607 |
rs757878121 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47525415 | ATTTGGTGACTAGGT[A/G]ACCTGCCTGTTTCAT | 23607 |
rs757922915 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47486850 | TAAATGTAGAAGCTC[A/G]TATACTGTATTTGTA | 23607 |
rs757924573 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47586563 | AGAAAATAACTGTCA[A/G]CCTATAGTTTTCTAC | 23607 |
rs757930895 | snp | C/G | 1.69381e-05 | 0.00291011 | missense | CD2AP | GRCh38.p7 | 6:47609129 | CGTTTTCAGCCATCT[C/G]TGTACCTTTCAACAC | 23607 |
rs757935168 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47614245 | GGGCAAAAGGCCAAT[C/T]TCTTGACCTGCTGTG | 23607 |
rs757944083 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47559457 | TTAAGAGATGGGGCC[C/T]CACTATGTTGACCAG | 23607 |
rs757959054 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47622003 | AGCTCACGCTCTTCT[C/T]GGGCGGGTCTTGCTG | 23607 |
rs758024609 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47485020 | CTCACTGTGTTTGTG[A/G]TGATGCTGGTGTCAA | 23607 |
rs758051274 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47524106 | CATTATTATATATAA[A/G]CCATGTTAATGTTTG | 23607 |
rs758072858 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47571667 | CAGTGAAACCCCAGA[A/G]ACTGAACATGAGCAG | 23607 |
rs758094493 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47587454 | CTACTTTCTGTCCCA[A/G]GCCACCACGTGGATT | 23607 |
rs758123465 | snp | A/C | 8.55176e-05 | 0.00653846 | utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47478237 | TTCTCCCCGCGGGAG[A/C]CCCCAGCATGGGTAA | 23607 |
rs758128311 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47537313 | TACCTTTTGAAAAAA[C/T]GAGTGTGTTGGTTCA | 23607 |
rs758164040 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47547287 | TCACCAACCCTCTGC[C/T]GCCTTCAAGAGACTC | 23607 |
rs758166745 | snp | C/T | 0.000149277 | 0.00863807 | missense | CD2AP | GRCh38.p7 | 6:47606257 | AGAAGGTTGCCGGGC[C/T]GTTTCAATGGTGGAC | 23607 |
rs758217944 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47480156 | TGTGTTTTGAAGGTA[A/T]GTTACTGAGGGCATT | 23607 |
rs758245156 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47606082 | CTTTTTAATTTATAG[-/T]TTGTCCAAAAACTGA | 23607 |
rs758258489 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47617356 | ATTTTGAATTCATCT[A/G]TACTCATGAATCTAA | 23607 |
rs758262794 | snp | A/G | | | synonymous-codon | CD2AP | GRCh38.p7 | 6:47503371 | GAATGTGAAAAAGCT[A/G]CAGGAGGAAGGGTGG | 23607 |
rs758277345 | in-del | -/TGTAT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47491268 | CCTGATATGTGTGTG[-/TGTAT]GTGTGTGTGTGTGTG | 23607 |
rs758327850 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47512861 | GCATAAACAAATAGT[A/G]TTTTGTGTGATTTAG | 23607 |
rs758334654 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47568035 | GAGACACGTGTAGAA[G/T]AGGATCTATATAAGT | 23607 |
rs758354988 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47593809 | GTTCCAAACGTCCAA[C/G]AGAATTGACAACAGA | 23607 |
rs758358828 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47496932 | GTATTTGTGGACTTA[A/G]CACTTTGTATGATAA | 23607 |
rs758359789 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47554824 | TATATAGCATCTAGT[A/G]TTTTATTTTGTATTT | 23607 |
rs758371908 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47555222 | ATTTTGTGATGTTAG[C/T]TATTTAGAGACTCAC | 23607 |
rs758386191 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47564485 | TTATGCTATTCAGCT[G/T]GATTTGGATTTTAGT | 23607 |
rs758392131 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47496235 | TATTTTCTTGGGTGT[A/G]GAGAGTTTAAGATTT | 23607 |
rs758392587 | snp | C/T | 1.64779e-05 | 0.00287031 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47574128 | GAGTGAAACTGCATC[C/T]GGATCAGTTACACAG | 23607 |
rs758430664 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47538984 | TTTTCTGAAATTTTT[A/G]AACTCTTGTGTGTCA | 23607 |
rs758432806 | snp | C/T | | | intron-variant, downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47603923 | TAATTTTACTGAAAG[C/T]GTACATGTCTGTCTG | 23607 |
rs758443398 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47595245 | GCTTATTTTCTTCTA[C/T]TTCAAATGGAAATAC | 23607 |
rs758443956 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47489094 | GGTAGTGAGTTATCT[C/T]GATTGCTTAGTCAGT | 23607 |
rs758447553 | snp | A/G | 1.65015e-05 | 0.00287237 | missense | CD2AP | GRCh38.p7 | 6:47595921 | CACAAGTCCCACCCA[A/G]GAAACCTACTCCACC | 23607 |
rs758470407 | in-del | -/AAA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47549461 | TTTTACAATAGCTGC[-/AAA]AAAAAAAAAAAAAAA | 23607 |
rs758475681 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47582384 | AAAAAATTCCTTAGA[A/G]TGTTGAAGACCCAGT | 23607 |
rs758482089 | in-del | -/AAAT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47501855 | TTATTAAAAGAGGTA[-/AAAT]AAATACATATTAATC | 23607 |
rs758497005 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47507659 | ACTATGTTGGCCAGA[C/T]TGGTCTCAAACTCCT | 23607 |
rs758500856 | snp | C/T | 1.67823e-05 | 0.0028967 | intron-variant | CD2AP | GRCh38.p7 | 6:47595824 | AAACCTAAATAATTT[C/T]GATTGTTAATAACTT | 23607 |
rs758523796 | snp | G/T | 3.31576e-05 | 0.00407157 | missense | CD2AP | GRCh38.p7 | 6:47533657 | CCATCAAACGGGAAA[G/T]GCATGGGAATGTAGC | 23607 |
rs758562758 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47568285 | CAACTTTTACTACCA[C/T]GTTGGCTATTCACTT | 23607 |
rs758595406 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47619092 | CTAATTTTTTTCCAT[A/C]CATTATTGGGGTAGA | 23607 |
rs758601330 | snp | A/C | | | intron-variant, downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47604404 | ACAGAAGACATTTTA[A/C]ATGAGCATGGTGTAT | 23607 |
rs758611676 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47611070 | AAACTGAATGGCAGG[-/T]TTTTTTTTTTTTAAT | 23607 |
rs758614765 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47533353 | GTTGGGGTGAGTGGT[A/C]GGGGTGGGGTTTGAG | 23607 |
rs758643904 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47598786 | GAAGGATAAAAGACT[A/G]CACATTGGGTACAGT | 23607 |
rs758645638 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47567557 | GCAGGAGAAATATTT[C/G]TTACAGGAAAGGGTG | 23607 |
rs758663817 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47553432 | GCTCACTGCAACCTC[C/G]GCTTCCCAGGTTCAA | 23607 |
rs758683074 | snp | G/T | 1.70388e-05 | 0.00291875 | intron-variant | CD2AP | GRCh38.p7 | 6:47503485 | TTGCTTCATAGGATT[G/T]AATCTTTAAATGTTA | 23607 |
rs758696839 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47614100 | TTAGATCTGCTATCT[A/G]GACCACTCAAACTTT | 23607 |
rs758701902 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47528970 | TCACTCTCTTGATAC[A/G]TTTGCTTTCTTAGTG | 23607 |
rs758707173 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47505947 | GCTGCCGGGCGGAGA[C/T]GCTCCTCACTTCCCA | 23607 |
rs758717684 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47516084 | AACCAAGATTTTATT[A/G]TACAGTTTAAGGAAA | 23607 |
rs758743814 | snp | A/G | 1.66427e-05 | 0.00288462 | intron-variant | CD2AP | GRCh38.p7 | 6:47576640 | CATATTGGGAATAGT[A/G]GAAACATACTCAAAT | 23607 |
rs758749739 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47500457 | GTTAAAATTTCTTGC[C/T]GGGTCCCTTATCATG | 23607 |
rs758753479 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47525523 | AGTAAATTGCTTTCT[A/T]TTTTCAAATCATGAT | 23607 |
rs758819395 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47499196 | TAAAGAGTCCTGATT[C/G]CTTTTAGTAGTAGGT | 23607 |
rs758827817 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47597945 | GACCCAGTGGTGTCT[C/G]TTCTTACCACATGCA | 23607 |
rs758874272 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47590618 | CAGGCACGTTCCACA[A/G]TGCTCACCATCGGGT | 23607 |
rs758877530 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47489164 | ACTGCACTCAACTAG[-/T]TTTTTTTTTTTTTTT | 23607 |
rs758878057 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47563281 | TATAAAATGACTTGC[A/G]TTACTTTAGGTAGGT | 23607 |
rs758883348 | in-del | -/GAC | | | intron-variant | CD2AP | GRCh38.p7 | 6:47588901 | GCACATTTACCTCTA[-/GAC]CAATGAAACTTATAA | 23607 |
rs758890916 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47502026 | TGCACTGAAGATGGT[G/T]GCCAGGGTTGGGTTC | 23607 |
rs758892279 | snp | A/C/G | 3.35465e-05 | 0.0040954 | synonymous-codon, missense | CD2AP | GRCh38.p7 | 6:47599346 | AAAATTTGAAACTGA[A/C/G]CCAGTATCAAAACTA | 23607 |
rs758894683 | in-del | -/GGG | 3.37501e-05 | 0.00410779 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624252 | CCTGGTGTTCATAAT[-/GGG]GTTCCAGGGATTCAG | 23607 |
rs758904597 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47518823 | CAATAGTTGTGACAG[A/G]CTTTTCAGTTTTATT | 23607 |
rs758905490 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47558030 | GTAGTTCTCCTTGAA[A/G]AGGTCCTTCACATCC | 23607 |
rs758962947 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47618310 | GGGTGACAGAACGAG[A/G]CTGTCTCAAAAAAAA | 23607 |
rs758969642 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47542289 | GATTGTTGGTGATAG[A/G]CTACTGATGGAGTGT | 23607 |
rs758989047 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47601090 | TTCTTTTTTTCGAAA[A/C]TTTTCCTATATAGTG | 23607 |
rs758996589 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47492475 | CTCCCCCGTTAGGCT[C/T]CCAAGTAGCTAGGAC | 23607 |
rs759008154 | snp | C/G | 1.66518e-05 | 0.00288542 | intron-variant | CD2AP | GRCh38.p7 | 6:47582083 | GAGGCTAATTTTCAA[C/G]TTTCAAAAAAGCAAT | 23607 |
rs759051078 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47618031 | TCTGATTAAAAGTAA[C/T]TTAGTGGCCGGGCAC | 23607 |
rs759069304 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47551484 | TTATGGTTGAAGCAT[G/T]GTGCTGAGAGTTTCA | 23607 |
rs759137727 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47526646 | ATGAACACAATGGAA[C/T]CAGGATTTGTATACA | 23607 |
rs759159416 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47529993 | GCCTGCTCATATGCT[A/G]TGCTTTCCTGTTAAG | 23607 |
rs759169325 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47557021 | TGATCGCCATTCTAA[C/G]TGGCATGAGATGGTA | 23607 |
rs759191007 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47575620 | ACACAGTAGTAGGTA[A/G]GTAAGTTAGCAGTGT | 23607 |
rs759192742 | in-del | -/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47525521 | CAAGTAAATTGCTTT[-/C]TATTTTCAAATCATG | 23607 |
rs759211721 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47615463 | CTCAGCTTCTGGGGA[A/G]GCCTCAGGGAGCTTT | 23607 |
rs759217794 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47579735 | TCTTTATTTTATAAT[G/T]TAAGAAGGGCTGTCT | 23607 |
rs759245162 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47530918 | AGAACTTATTTACAA[C/G]GTAATAGCTTTTTTA | 23607 |
rs759274707 | snp | A/C | 3.30316e-05 | 0.00406383 | missense | CD2AP | GRCh38.p7 | 6:47503423 | AGAAGAGGAATGTTC[A/C]CTGACAATTTCGTTA | 23607 |
rs759290520 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47575127 | GGAAAGAGAACTTCC[A/G]CTTTCTATCCTACAT | 23607 |
rs759293486 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47517242 | GAAGAGATGCTGGAG[C/T]CATGCTTGTATAGCT | 23607 |
rs759299287 | in-del | -/TTTTTTTT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47553514 | ACCACACCTAGTGAA[-/TTTTTTTT]TTTTTTTTTTTTTTT | 23607 |
rs759307654 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47526045 | TACTGCAATGTTAAT[A/G]TGTATGCTATTTCCT | 23607 |
rs759309620 | snp | A/T | 0.000496738 | 0.0157519 | missense, intron-variant | CD2AP | GRCh38.p7 | 6:47576596 | GATACCGAAGGTAAA[A/T]TTAAAGGTATGTTTT | 23607 |
rs759313600 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47544945 | CTAAGTAGTTAAGAA[C/T]GTAAACAAGCCTTTT | 23607 |
rs759338149 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47623424 | TAAAAACCATGGGCT[C/T]TAAAGCCCTAAATCT | 23607 |
rs759345666 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47513662 | CCGGCTAAGTATTAC[A/T]TATTTTTTGGATATT | 23607 |
rs759393282 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47487836 | TAACACTTGTATTGA[C/G]TAGCAGAAAATTAGG | 23607 |
rs759432867 | snp | A/T | 0.000155024 | 0.00880273 | intron-variant | CD2AP | GRCh38.p7 | 6:47599294 | GCGTGTTTTTTTCTT[A/T]TTTCAGGATTAATGG | 23607 |
rs759436440 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47573134 | GTAGGGTTGTTTGTG[A/G]ACTCATTGAGCCTAT | 23607 |
rs759439653 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47598204 | CCGCAATGTGATACC[A/G]CCTCACTTCTGCAAG | 23607 |
rs759475634 | snp | A/G | 3.37752e-05 | 0.00410932 | intron-variant | CD2AP | GRCh38.p7 | 6:47544746 | AAAACAGTAATGGTA[A/G]TTGATGCTATGGATT | 23607 |
rs759501591 | in-del | -/AACAAA | 3.30841e-05 | 0.00406706 | cds-indel | CD2AP | GRCh38.p7 | 6:47576571 | TCAGAGTGTGGAGAT[-/AACAAA]AACAGATACCGAAGG | 23607 |
rs759506071 | snp | G/T | 1.68448e-05 | 0.00290209 | missense | CD2AP | GRCh38.p7 | 6:47599409 | AAAATCAGTAGACTT[G/T]GATTCACTTACAGTA | 23607 |
rs759515842 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47552533 | TATATATACACACCA[C/T]ATATTTTTAAATTCA | 23607 |
rs759554468 | in-del | -/TCTAAAATCTAA | 1.64966e-05 | 0.00287194 | cds-indel | CD2AP | GRCh38.p7 | 6:47503419 | GGGAGAAGAGGAATG[-/TCTAAAATCTAA]TTCCCTGACAATTTC | 23607 |
rs759575603 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47538085 | TACGACTGTATGAAT[G/T]GCTGATTGATACATA | 23607 |
rs759589454 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47486616 | ACTTCTGGCAAAGAG[G/T]CTTTAGAATGAAGTA | 23607 |
rs759604029 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47548131 | ACAGACCATTTAAGG[A/G]CACCTCAAGAAACGA | 23607 |
rs759613060 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47498514 | CATGGTTAATTCCCC[A/G]TTTTTTTCTCCTTGA | 23607 |
rs759621262 | snp | A/G | 1.78058e-05 | 0.00298372 | missense | CD2AP | GRCh38.p7 | 6:47612475 | ACTTTGTTTTTAGGA[A/G]AGAACTGGAAAAACT | 23607 |
rs759649903 | in-del | -/GACA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47607127 | ATCCATGTTGCAAAT[-/GACA]GGATCTCATTCTTTT | 23607 |
rs759702616 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47547378 | ACAGCAGGAGTAGCT[A/G]TGCTTATATCAGACA | 23607 |
rs759704116 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47583161 | CAAAAGTACAGAGTT[C/G]CTGTATACTTCCTTT | 23607 |
rs759790957 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497466 | TGGTGCGATCTCTGC[C/T]CATTGCAGCCTCCAC | 23607 |
rs759799770 | snp | C/T | 1.65334e-05 | 0.00287514 | intron-variant | CD2AP | GRCh38.p7 | 6:47544603 | TTATGTTACTTTCTT[C/T]AGAGACCAAGAAGCG | 23607 |
rs759848316 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47556177 | CCGTCATCTACATTA[C/G]GTATTTCTCCTAATG | 23607 |
rs759855730 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47519847 | GAACTTTTCAAATTG[C/T]CCTTTTAAAAGAAGT | 23607 |
rs759885985 | snp | C/T | 1.69677e-05 | 0.00291266 | intron-variant | CD2AP | GRCh38.p7 | 6:47579504 | AGTAAGCTTTTGTTT[C/T]TCAATGATGATAATA | 23607 |
rs759886651 | snp | A/T | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625481 | CTTCAGAGTTACTTA[A/T]GAACAGTTGAATGCT | 23607 |
rs759909168 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47482000 | TCTTGGCCTCAAGCA[A/G]TTCACCTGCTTTGGC | 23607 |
rs759941391 | snp | C/T | 1.67871e-05 | 0.00289711 | intron-variant | CD2AP | GRCh38.p7 | 6:47579377 | AATTATTCTATTTTG[C/T]TTTTTAGGAGACTGG | 23607 |
rs759967318 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47607019 | GTTCTCTATCTCCAT[C/T]AGTTCAGTTGTTTTA | 23607 |
rs759969710 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47510029 | TTCCTGTTTCAGTAT[A/G]ACTAATACTAGAAGT | 23607 |
rs759994758 | snp | A/G | 1.72913e-05 | 0.0029403 | intron-variant | CD2AP | GRCh38.p7 | 6:47606327 | TTTAGCAAATGCAGA[A/G]TCCATTGGAAGATAG | 23607 |
rs760002947 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47605577 | TAATGTCTAAACAAA[A/G]GTGCAGTGAACTATA | 23607 |
rs760034318 | snp | C/T | 8.64043e-05 | 0.00657227 | utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47478228 | GACGTCGGCTTCTCC[C/T]CGCGGGAGCCCCCAG | 23607 |
rs760049178 | in-del | -/T | 5.27412e-05 | 0.00513496 | intron-variant | CD2AP | GRCh38.p7 | 6:47624172 | TTTGCTCAATTTATG[-/T]TTTTTTGTTTTAGAT | 23607 |
rs760050189 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47600235 | AAGCTACAGACACAT[C/T]AAATAAGCACTATCA | 23607 |
rs760077449 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47621033 | ATTTGGATGCCCTTT[A/G]TTTATTTCTCTGCTC | 23607 |
rs760077912 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47568160 | GGAGATGTCATTTGC[A/G]GAGATAGGATATTGG | 23607 |
rs760091472 | in-del | -/TTTTTTTTTT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47489970 | TTCTCTAAAGAGACT[-/TTTTTTTTTT]TTTTTTTTTTTTAAA | 23607 |
rs760104782 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47622952 | GTAGTAGCCTTCACA[C/G]TCCCTACTCCCTCTT | 23607 |
rs760110147 | snp | C/T | 6.59022e-05 | 0.00573993 | missense | CD2AP | GRCh38.p7 | 6:47574100 | CTTCACCTATACCTT[C/T]TCTGGGAAATGTGAG | 23607 |
rs760168200 | snp | C/T | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521770 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCTGAGG | 23607 |
rs760171131 | snp | A/T | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476281 | ATTATTGCCTTCCCC[A/T]AGCTTTCGTTCAACT | 23607 |
rs760189473 | snp | A/G | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47477682 | GGCAGCAGCCGTGGG[A/G]ACCGGGAGAGAGCCC | 23607 |
rs760223406 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47579537 | TGAAAGAACATTTTG[C/T]CACTATTCTTTTGCA | 23607 |
rs760245149 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47598404 | CCCACTACTGGGTAT[C/T]TACCCAGAGGAAAAT | 23607 |
rs760269835 | in-del | -/T | 3.32682e-05 | 0.00407836 | intron-variant | CD2AP | GRCh38.p7 | 6:47503260 | ATTTTAGACATTTCG[-/T]TTTTTTCCCCCTTTT | 23607 |
rs760281402 | snp | C/T | 1.6489e-05 | 0.00287128 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47609278 | TGAATTGTTGTGCAT[C/T]GTAGAAGCACTGAAA | 23607 |
rs760287713 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47541833 | ACTTCCAGTACAGCT[C/G]ATATTTCTATTGTAG | 23607 |
rs760353599 | snp | C/T | | | downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47627742 | ACAAAAAGAGCTAAT[C/T]TCAGCATGGGAGCTC | 23607 |
rs760404986 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47559730 | CTTGACACTTTTGTC[C/T]TCATCCATAATTATG | 23607 |
rs760419274 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47493705 | TTTATACCTCTTGAA[A/G]TTTTTCACAGTTCTT | 23607 |
rs760419409 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47578108 | TGTATGTGAATTTTC[A/G]TATTAATATAATTTG | 23607 |
rs760426418 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47587193 | TTGAAGCGTCTTAAG[A/C]CTTCCACCAAGGAAA | 23607 |
rs760429619 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47528722 | CAAAAAGGGTCACAA[C/G]TTTAGAGGTAAGTCT | 23607 |
rs760439714 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47605078 | TCTTTTTAAAGAAAC[-/A]AAATAACTGAGTTAG | 23607 |
rs760459506 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47548974 | ATCATCTCAATAGAT[A/G]CAGAAAAAACATTAG | 23607 |
rs760472244 | snp | G/T | 1.66316e-05 | 0.00288367 | missense | CD2AP | GRCh38.p7 | 6:47533639 | TCAAGGATGACAGTT[G/T]GCCCATCAAACGGGA | 23607 |
rs760472374 | snp | A/G | 1.6534e-05 | 0.00287519 | missense | CD2AP | GRCh38.p7 | 6:47609171 | TCTAAAGCAAATACA[A/G]CTGCTTTCCTGACTC | 23607 |
rs760490116 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47524907 | TCTATTGACACTTAG[A/G]CGATACGTACTGATT | 23607 |
rs760499417 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47613568 | ATATTCAGTAAATCA[A/T]GCTGTAAACAGATGT | 23607 |
rs760513125 | snp | A/G | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521673 | ATTCAGCAAAAAGCT[A/G]ATAAACGTAGTTGAT | 23607 |
rs760544587 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47484352 | ACTTGATATTACCTC[C/T]TTTTTTTTTTTTTGT | 23607 |
rs760546509 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47486505 | TATTAGAATATAGAT[G/T]CCTGCACTGAAGGAA | 23607 |
rs760557949 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47571405 | AACAAGGGGAAAGGA[C/G]AGCTCTACCATTGTC | 23607 |
rs760564639 | in-del | -/TTTTTTTTG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47489180 | TTTTTTTTTTTTTTT[-/TTTTTTTTG]AGAAGTCTCGCTCTT | 23607 |
rs760602704 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47599883 | TTCCAGTGGAGGAAA[A/C]TATGCTTTTTCTAAC | 23607 |
rs760611351 | in-del | -/A | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626553 | TTTGAGACACACAGT[-/A]ATCATTAATTTCTGA | 23607 |
rs760621552 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47479495 | CAGGTAACTTTCATA[C/T]TCAAAAGTGCTCTTG | 23607 |
rs760637487 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47576130 | TCCAGGCTGGAATGC[A/G]GTGGTACAATCATAG | 23607 |
rs760641662 | in-del | -/ACTC | | | intron-variant | CD2AP | GRCh38.p7 | 6:47571055 | TGGCCTTAATCAAAT[-/ACTC]AAACTGTGAAAATTG | 23607 |
rs760653572 | snp | C/T | 1.65792e-05 | 0.00287912 | intron-variant | CD2AP | GRCh38.p7 | 6:47576608 | AAAATTAAAGGTATG[C/T]TTTTGAATAAAGCTT | 23607 |
rs760655519 | snp | C/T | 1.82274e-05 | 0.00301883 | intron-variant | CD2AP | GRCh38.p7 | 6:47606157 | TAATGTTTATTTTTA[C/T]TTTCTAGATGTTGTA | 23607 |
rs760682604 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47586222 | AAAAACTGGAAAATA[G/T]AAGAAAGACCCAAAT | 23607 |
rs760711476 | in-del | -/TTTCC | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497307 | TGTTCCCGTTCCCTT[-/TTTCC]TTTCCTTTCCTTTCC | 23607 |
rs760732417 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47501419 | TTCAGCTGACCTGAT[C/T]GTACTTAGTGTCTGA | 23607 |
rs760735034 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47550988 | GCTAAGCTATGAGGA[C/T]GCAAAGGCATAAGAA | 23607 |
rs760735382 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47513538 | TAATAAGTGGTATTT[C/T]AGTGTTTTTTTTTCT | 23607 |
rs760737495 | in-del | -/TTCTC | 1.65002e-05 | 0.00287225 | intron-variant | CD2AP | GRCh38.p7 | 6:47609321 | TAAGTAGCCCTTCTT[-/TTCTC]CTGTGAGTACTACTT | 23607 |
rs760766770 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47496326 | TGTTGCTAAGTCACC[A/C]ATTAGTCTGAATGTT | 23607 |
rs760777753 | in-del | -/TTC | | | utr-variant-3-prime, cds-indel | CD2AP | GRCh38.p7 | 6:47625964 | GTCAAATGAATTATT[-/TTC]TTCTTGTTAAATAAA | 23607 |
rs760778741 | snp | A/C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47588465 | GATTCCAGATTATGA[A/C/T]GTGTTTACATTTGTT | 23607 |
rs760791523 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47561441 | AACCTTCCCTACCCT[A/G]GTCTTGGAATCAGCT | 23607 |
rs760797223 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47608729 | TCCTGGACCTATTAA[A/G]TTGTTCACAATTACT | 23607 |
rs760818669 | snp | A/C | 1.6914e-05 | 0.00290805 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624258 | TGTTCATAATGTTCC[A/C]GGGATTCAGAAGCAA | 23607 |
rs760819944 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47523709 | GTTGGAGAAATACTT[C/T]ATACAGGTAATACTA | 23607 |
rs760855710 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47594825 | ATAGTATTTTGTATT[C/T]ATTGTGAAATAAGAC | 23607 |
rs760856329 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47512227 | TGCGCCTGTAGTCCC[A/T]GCCACCCAGGAGGCT | 23607 |
rs760870001 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47590512 | CTATATGGGGTCCAC[A/G]TATACACAGATTTTT | 23607 |
rs760877207 | snp | C/G | 1.65143e-05 | 0.00287348 | intron-variant | CD2AP | GRCh38.p7 | 6:47580909 | GCTCCAGGTATGTAA[C/G]AAGCATATTATTCAG | 23607 |
rs760878947 | snp | C/T | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520401 | AGTGCCTCACTTGGT[C/T]TCTGTTGACAGTTGT | 23607 |
rs760909944 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47617892 | ACAATTGATAAGTCC[A/G]AATTTTTATTCTTAC | 23607 |
rs760920127 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47481055 | GTATTCTGTGTGAAA[C/G]AATTTGGGAAGAGCT | 23607 |
rs760935840 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47525908 | TTGAAGTATGAAACT[C/G]GAGTTTTTCAGAGTT | 23607 |
rs760951876 | snp | C/T | 1.76188e-05 | 0.00296801 | intron-variant | CD2AP | GRCh38.p7 | 6:47624171 | TGTTTGCTCAATTTA[C/T]GTTTTTTGTTTTAGA | 23607 |
rs760969524 | snp | C/T | 9.30605e-05 | 0.00682067 | missense | CD2AP | GRCh38.p7 | 6:47554764 | AAGCCCAGGACGATT[C/T]AGGTAGACTATTTTT | 23607 |
rs760979990 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47560961 | ATTTTACTCTAAAGA[C/G]AAACTTTTGTCTTTC | 23607 |
rs760984874 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47568080 | CAGGACCTAGTGATA[A/G]TGTTATTTGGGGGAT | 23607 |
rs760996817 | snp | G/T | 6.61146e-05 | 0.00574917 | intron-variant | CD2AP | GRCh38.p7 | 6:47554604 | GTGACGATTTTCACT[G/T]AACAGAAGTTGTTTT | 23607 |
rs760999567 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47610351 | ATGAGAGTGAGGGTG[C/T]TCATCCCTTGTCTTC | 23607 |
rs761012304 | snp | C/T | | | intron-variant, utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47603869 | CAATCAAAATAGTAT[C/T]TTCAATATAAATAGG | 23607 |
rs761043089 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47498233 | ATTTGGCAGAGTATG[C/T]AATTAATTTTCCTTC | 23607 |
rs761064199 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47581867 | TGAGCCTGGTAATTC[C/T]GGTACATTGTTCTTT | 23607 |
rs761081784 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47596310 | AGCATTTTTAAAGAA[C/T]GCGGTACATCACATT | 23607 |
rs761118197 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47619826 | CGATCATTAGTGATG[C/T]TGAGCATTTCTTCAT | 23607 |
rs761164894 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47581453 | GATTTGCTGTTTTTT[A/T]AGAATAATTCAAGTC | 23607 |
rs761165939 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47541461 | TTATTATAAAAACTA[C/T]AATAAAAAATCAGAT | 23607 |
rs761181242 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47582795 | GTTTTTTTTTGTTTT[G/T]TTTTTTTTTTTTTGT | 23607 |
rs761183938 | snp | A/C | 0.000256312 | 0.0113177 | utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47478235 | GCTTCTCCCCGCGGG[A/C]GCCCCCAGCATGGGT | 23607 |
rs761193505 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47537700 | TATTGAGTGTCTTAA[A/G]TAGAACATCTCAGCA | 23607 |
rs761197922 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47479873 | TGATTAGTGTCCCCC[A/G]TCATCTTTCCTTTTC | 23607 |
rs761201804 | in-del | -/TG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47556787 | TGCATTAAACATATG[-/TG]TGTGTGTGTGTCTTT | 23607 |
rs761237518 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47546926 | TATCCAGCAAAACTT[A/G]GCTTCATAAATGAAG | 23607 |
rs761254714 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47547840 | TCTCTCACACCACAG[C/T]GAAATAAAACTGGAA | 23607 |
rs761281468 | snp | A/G | 1.65105e-05 | 0.00287315 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47607998 | CCTGAAGCCATCTGA[A/G]TTAAAAAAAGATACA | 23607 |
rs761292392 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47601308 | TGATTTGTTCTTTTC[C/T]TTCAATAAATAAGGA | 23607 |
rs761352261 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47527309 | TCCCTTCCCACCTCC[C/T]ATGGATCAACTGAAA | 23607 |
rs761363856 | snp | A/C | 1.64982e-05 | 0.00287208 | missense | CD2AP | GRCh38.p7 | 6:47574200 | AGAAGGCTCTGTGAA[A/C]CTTCGGACAAGAACA | 23607 |
rs761394311 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47592557 | GATAAAGGTGAGAGG[-/A]ACATCTTTTGTTATT | 23607 |
rs761433355 | in-del | -/TTTTTTTTTT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47489969 | TTCTCTAAAGAGACT[-/TTTTTTTTTT]TTTTTTTTTTTTAAA | 23607 |
rs761446441 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47522776 | AATTATCTTTTATTT[-/A]AAAATGTTTATTTTC | 23607 |
rs761464567 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47540953 | AACAACTTGCAAAGG[-/T]TATTTAGGGACACTA | 23607 |
rs761500438 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47554620 | AACAGAAGTTGTTTT[A/T]GCTTTTGAATTGTGA | 23607 |
rs761525346 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47501282 | TTGAAAACCATTCAC[C/T]GTGTATGTTTAATTG | 23607 |
rs761529341 | in-del | -/ACCCT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47565690 | TCTTTTTAACCTCGC[-/ACCCT]ACCATGATTCATTAA | 23607 |
rs761535745 | in-del | -/AAAA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47551188 | AACCTATGGAAATAA[-/AAAA]AAGAAAAAAAAATTT | 23607 |
rs761537974 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47599743 | GACTGTACTACCCAA[C/T]GGAGATATGAATACA | 23607 |
rs761556396 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47604902 | ACAAAGAAATTGCTA[G/T]AAAAAATTATCAGCA | 23607 |
rs761581258 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47507634 | GTATTTTCAGTAGAG[A/C]TGGGCTTTCACTATG | 23607 |
rs761596642 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47539781 | TACCTCCTTTATTCT[C/T]TTCCTTGTTAGTAGC | 23607 |
rs761603787 | snp | C/T | 3.2994e-05 | 0.00406152 | missense | CD2AP | GRCh38.p7 | 6:47596011 | AACCAGTTCCTCCAC[C/T]ACCTCCTATAGCCAA | 23607 |
rs761656861 | snp | C/G | 1.65105e-05 | 0.00287315 | missense | CD2AP | GRCh38.p7 | 6:47595914 | GCAGCTCCACAAGTC[C/G]CACCCAAGAAACCTA | 23607 |
rs761663920 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47500186 | TTTTTTGTAGATTAA[C/T]CCTTCAGTTTTTTGC | 23607 |
rs761664108 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47496425 | TACAAACTTAATTAT[A/G]AATAAGTTTAAAAGA | 23607 |
rs761676625 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47487211 | AGCAGATCAAAACAA[-/T]TTTTTTAATGATGAA | 23607 |
rs761713967 | snp | A/G/T | 3.29844e-05 | 0.00406095 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47609290 | CATTGTAGAAGCACT[A/G/T]AAAAAGGATCACGGG | 23607 |
rs761728768 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47613680 | CAGAATGATAAATAA[C/G]TGATGGTTTCCATTA | 23607 |
rs761734055 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47510297 | CTCAGCTCTTATTGC[A/T]GAGAGGGCCTAGAAG | 23607 |
rs761757240 | snp | C/T | 4.97855e-05 | 0.00498902 | missense | CD2AP | GRCh38.p7 | 6:47533650 | AGTTTGCCCATCAAA[C/T]GGGAAAGGCATGGGA | 23607 |
rs761772327 | snp | C/G | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476255 | TCAGTTCTAGGACTC[C/G]TCCAGACTGAATTAT | 23607 |
rs761783895 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47614893 | CATTTAAACTTAAGA[A/G]TTTATCTTAATTCTC | 23607 |
rs761792087 | snp | A/G/T | 5.91726e-05 | 0.00543906 | intron-variant | CD2AP | GRCh38.p7 | 6:47579354 | AAAAAAAAAAGGTCT[A/G/T]TTGTCTTAATTATTC | 23607 |
rs761810631 | snp | A/G | 1.65146e-05 | 0.0028735 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47577028 | AGAATATTGTAGAAC[A/G]TTATTTGCCTATGAA | 23607 |
rs761835131 | snp | A/G | | | intron-variant, downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47604184 | TGATTGCAAAAGCTA[A/G]ATGATTGTCGTGCCT | 23607 |
rs761837706 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47598426 | GAGGAAAATAAGTTA[C/T]TATATGAAAAAGATA | 23607 |
rs761889675 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47515757 | CTTAGCATTATAAAA[C/T]TAAAAGTGCTTTTGA | 23607 |
rs761924278 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47621347 | TGGTATATCACATTT[A/G]TTGACTTGTGTATGT | 23607 |
rs761934194 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47585998 | TTCAAGAGAGTAAAA[A/G]TCACGGCGTCCATTG | 23607 |
rs761977297 | snp | A/T | 1.74011e-05 | 0.00294962 | intron-variant | CD2AP | GRCh38.p7 | 6:47599455 | ACAGGTAAGTCAGCA[A/T]GGACAGCGGTGGTGC | 23607 |
rs761996388 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47535792 | TCTGTGCTGAGGGAG[A/G]ATTTTTAGGCCCACG | 23607 |
rs762020246 | snp | A/C | 3.33745e-05 | 0.00408487 | missense | CD2AP | GRCh38.p7 | 6:47554746 | ATGATGGTGAAACTC[A/C]TGAAGCCCAGGACGA | 23607 |
rs762028392 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47531364 | CACAGAAACTGAAAG[A/T]AAAAACATTTATTCT | 23607 |
rs762034400 | snp | A/G | 1.69663e-05 | 0.00291253 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624266 | ATGTTCCAGGGATTC[A/G]GAAGCAACGCTATGA | 23607 |
rs762041010 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47570242 | CTTTTAAGTCACTTT[A/G]TATGAAGATACAAGC | 23607 |
rs762078976 | snp | A/G | 3.33189e-05 | 0.00408146 | missense | CD2AP | GRCh38.p7 | 6:47606183 | TTGTAAATTTTGATG[A/G]CATAGCTTCCTCAGA | 23607 |
rs762122439 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47565858 | TAGCCAGTAGTGATC[A/G]CCCTCCAGTAGCTTT | 23607 |
rs762126520 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47518353 | CATTCATTATCTGCA[A/G]AAGTTAGTGTTCTAC | 23607 |
rs762133376 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47622335 | CCAGATTTGCCGCCC[G/T]ACCCAGAGTTGTGGC | 23607 |
rs762150438 | in-del | -/ATA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47551905 | GTCGTCGGACTTACT[-/ATA]TGGCAGTTCACGGCT | 23607 |
rs762201290 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47519066 | TTTTATAGGTGGCAA[G/T]AACACAACTGTGAAT | 23607 |
rs762203408 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47581240 | ATTTGTTAATGTCTC[A/G]AATAATAATTTATGT | 23607 |
rs762207582 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47486103 | TCATCAAGCAAAGAA[A/G]CTGCTGGTGAGAGTT | 23607 |
rs762216291 | snp | C/T | 1.65446e-05 | 0.00287612 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47582055 | TTTTTCTTTAAAGCC[C/T]GAAGAAAAGGGTGAG | 23607 |
rs762237115 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47574369 | AGATCACTAATAATT[C/T]GGTTATGAATGAGGA | 23607 |
rs762264070 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47478417 | GCCTTCCACCTTGCT[C/G]TTCTCACGGAGAAAC | 23607 |
rs762265505 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47513350 | TCTTCAGTCATGACT[C/G]CTTGGGCAGTCTAAG | 23607 |
rs762272718 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47532916 | ATGTCTTCCAGTAAA[A/G]TTTTATACTTTTCCA | 23607 |
rs762278119 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47617010 | AGTCACTCTGTCACC[C/T]AGGCTAGAGTACAGT | 23607 |
rs762300203 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47553009 | TTTTTTTATTCTTTC[A/C]AGCCCTTTCTGTTTG | 23607 |
rs762326780 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47616331 | ACTCCTGACCTCAGG[C/T]GATCCACCTGCCATG | 23607 |
rs762348849 | snp | C/T | 1.66322e-05 | 0.00288371 | missense | CD2AP | GRCh38.p7 | 6:47609145 | TGTACCTTTCAACAC[C/T]TTCCAGTGCTTCTAA | 23607 |
rs762372736 | snp | C/T | 1.65206e-05 | 0.00287403 | intron-variant | CD2AP | GRCh38.p7 | 6:47554618 | TTAACAGAAGTTGTT[C/T]TTGCTTTTGAATTGT | 23607 |
rs762402753 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47588345 | ATACCTGTACCTTAC[-/T]TTGCCATTGGTTCTC | 23607 |
rs762405446 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47515404 | AAATGAAGGGGATAG[A/G]TAATAGGCTAATAAC | 23607 |
rs762407927 | snp | A/T | 1.72338e-05 | 0.00293541 | intron-variant | CD2AP | GRCh38.p7 | 6:47608080 | TGGGATTCTTTGTGG[A/T]CATCAAACATAGGGA | 23607 |
rs762449801 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47495534 | CTGCTGTAGGAGACT[A/G]CTAGTGTTCCTGCTA | 23607 |
rs762454933 | in-del | -/TTG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47499737 | GAGTTAAGAGTTTTG[-/TTG]TTGTTGTTGTTGTTG | 23607 |
rs762462715 | in-del | -/TA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47485632 | AAATCTATAGTAGTG[-/TA]TATACTAATGTCCTA | 23607 |
rs762462951 | snp | A/G/T | 3.30563e-05 | 0.00406538 | missense | CD2AP | GRCh38.p7 | 6:47608008 | TCTGAATTAAAAAAA[A/G/T]ATACATGCTACTCTC | 23607 |
rs762501100 | snp | C/G | 4.94776e-05 | 0.00497357 | missense | CD2AP | GRCh38.p7 | 6:47503415 | TAAATGGGAGAAGAG[C/G]AATGTTCCCTGACAA | 23607 |
rs762505120 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47538362 | TTCTCCTGCCCCAAC[A/G]TCCCAAGTAGCTGGG | 23607 |
rs762516903 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47567953 | GACTGAGCTGCTGAC[A/G]CCAGTTGAGAATGTT | 23607 |
rs762574705 | in-del | CACACACACACACAC/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47532406 | ACACACACACACACA[CACACACACACACAC/T]AATACTTGCCATATC | 23607 |
rs762608762 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47581558 | ATTTTTATAGAAGTT[A/G]GTGTTGAAAGCTTTT | 23607 |
rs762624600 | in-del | -/T | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476072 | AATTTACTACCTATG[-/T]TATGTGCTTCCAATA | 23607 |
rs762643913 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47504081 | AGTCGCTTCTGCCAG[A/G]AAACAATCTTTAGGG | 23607 |
rs762646099 | snp | C/T | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520295 | TTATAACAGTCAATA[C/T]TGGTTGAGGACCTTG | 23607 |
rs762652625 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47567176 | CATTTGTTTGCTGCT[A/G]TCTTCATCTAATTTT | 23607 |
rs762661708 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47503266 | AGACATTTCGTTTTT[C/T]CCCCCTTTTTTAGTT | 23607 |
rs762662122 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47579566 | CAAACAAGTTTTTTT[A/G]CATTATTATTGAATA | 23607 |
rs762663715 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47603539 | GCTTAATGCATATTG[A/G]AATTAATACTAATAT | 23607 |
rs762669222 | snp | C/G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47552980 | TTGTCATTTCCTTTT[C/G/T]GGGGGGAGCATTTTT | 23607 |
rs762679795 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47515627 | CTATGGTATGTGCTA[G/T]TTATTAGAGAAATGT | 23607 |
rs762719680 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47503073 | TTGAGGCTCCCACTT[A/G]ATAGCTGTATTGTAC | 23607 |
rs762737431 | in-del | -/TT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47496273 | TTTTCTTTCCACACA[-/TT]TAAGATACTAATCTG | 23607 |
rs762742761 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47514604 | TATTTTGGGGTGTGG[A/T]GAGAAGAATCTTTCC | 23607 |
rs762745837 | snp | C/T | 1.66432e-05 | 0.00288467 | intron-variant | CD2AP | GRCh38.p7 | 6:47576477 | TGTTTAACAGTATTA[C/T]CTTTATTCTATCTTA | 23607 |
rs762767931 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47526405 | ACATCTCAGTTGGCA[A/G]TATGTATTTGGAAGG | 23607 |
rs762773136 | snp | C/T | 1.75816e-05 | 0.00296488 | intron-variant | CD2AP | GRCh38.p7 | 6:47599280 | TACTAGTGATTTTTG[C/T]GTGTTTTTTTCTTAT | 23607 |
rs762774354 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47528289 | AAGTGATTCTCATAC[C/T]TCATCCTCCCAAGGA | 23607 |
rs762774473 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47570522 | CCTCCTTTTTCCTTT[C/T]TCCTTGCTCCTTATC | 23607 |
rs762800934 | snp | A/G | 1.64999e-05 | 0.00287222 | missense | CD2AP | GRCh38.p7 | 6:47574207 | TCTGTGAAACTTCGG[A/G]CAAGAACATCCAGTA | 23607 |
rs762821541 | snp | C/T | 1.65927e-05 | 0.00288029 | intron-variant | CD2AP | GRCh38.p7 | 6:47544591 | TCTAATTTCTTATTA[C/T]GTTACTTTCTTTAGA | 23607 |
rs762851253 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47528128 | ATGCATGTACTGTAG[C/T]TTATTTAAATAGTTC | 23607 |
rs762866445 | snp | A/C | 3.76117e-05 | 0.00433641 | intron-variant | CD2AP | GRCh38.p7 | 6:47612457 | GACTTAACAGTAATA[A/C]GTACTTTGTTTTTAG | 23607 |
rs762872003 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47594909 | ATAATCACCAGTTTC[C/T]GGTTGATATGAAATC | 23607 |
rs762874586 | snp | A/G | 1.66877e-05 | 0.00288852 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47579489 | TGATAAAGACTTTCC[A/G]GTAAGCTTTTGTTTT | 23607 |
rs762889642 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47576426 | CCTAGCTATAAGTAC[C/G]ATTAGGGAAAGCTGG | 23607 |
rs762906886 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47490485 | AGTGGGAAGATGAAG[A/C]ATGATAATATTTAAT | 23607 |
rs762931465 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47539886 | GTTACTTATGATAAG[-/A]AAATACTAATAGCTG | 23607 |
rs762954797 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47539622 | AGCTATGTAGTCTTT[A/G]ATGGATTATTTAACT | 23607 |
rs762969387 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47584954 | GTTTTGTTAAAATTC[A/G]GATAGTGACTTCCCC | 23607 |
rs762969481 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47609863 | TAGAAATCTTCTGGT[C/T]GGATATGATTAGTTT | 23607 |
rs762977929 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47620275 | GTTTCATTCTCCTAC[A/G]TGCGGCTAGCCAATT | 23607 |
rs763034719 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47621133 | TTTCAGTTCTCAGAG[A/G]GAATGCTTTCAACTT | 23607 |
rs763045932 | snp | A/T | 1.67761e-05 | 0.00289617 | missense | CD2AP | GRCh38.p7 | 6:47533746 | CCACAAACCAAAAAC[A/T]TTAAGAAGAGTATGT | 23607 |
rs763046550 | in-del | -/A | 4.73541e-05 | 0.00486568 | intron-variant | CD2AP | GRCh38.p7 | 6:47533554 | TTGAGGATTTAATAT[-/A]AAAAAATATAACTTA | 23607 |
rs763049845 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47569529 | CATTTATCCCTCTAG[A/G]CTTTACCGGGCAACT | 23607 |
rs763090495 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47585717 | TTGCCTGAATATTGA[A/T]CTACACATGCATGAA | 23607 |
rs763112070 | in-del | -/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47572518 | TCACTATACTTGTTA[-/G]CATTATATTTCTTAA | 23607 |
rs763126564 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47499984 | TCCACCCACCTCAGC[C/T]TCCCAAAGTGCTGGG | 23607 |
rs763126675 | snp | A/G | 3.30235e-05 | 0.00406333 | missense | CD2AP | GRCh38.p7 | 6:47577045 | TATTTGCCTATGAAG[A/G]TACTAATGAAGATGA | 23607 |
rs763151144 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47534501 | CACCTGAGGTCAGGA[C/G]TTCGAGACCAGCCTG | 23607 |
rs763158989 | in-del | -/TTT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47532951 | GGTTCACATGTCTTA[-/TTT]TATAGCCATGACTTA | 23607 |
rs763172753 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47544759 | TAATTGATGCTATGG[A/G]TTTTAGAAAAATTAA | 23607 |
rs763227419 | snp | A/T | 1.75231e-05 | 0.00295994 | intron-variant | CD2AP | GRCh38.p7 | 6:47579366 | TCTATTGTCTTAATT[A/T]TTCTATTTTGCTTTT | 23607 |
rs763228294 | snp | A/C | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476507 | CATAATGCTGAACAC[A/C]TATTTGTTACCTAAA | 23607 |
rs763266176 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47598260 | AAATAATAGATGTTA[A/G]CATGGATGCAGTGAA | 23607 |
rs763267844 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47583329 | GTTGTAACTATTATG[G/T]ATTTTGACAAATGTA | 23607 |
rs763268756 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47578364 | GCATCCCATTGCGCC[G/T]GATTAATTCTTTTTT | 23607 |
rs763283524 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47560569 | GTTTGTTTGTTTGTC[-/T]TTTTTCCCCCGATTC | 23607 |
rs763296631 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47541540 | AACTTTCTTATTTGG[A/C]GACTCAATTATTTTA | 23607 |
rs763307283 | snp | A/G | 3.39127e-05 | 0.00411767 | intron-variant | CD2AP | GRCh38.p7 | 6:47606309 | GTCGTAAACTACAGT[A/G]TATTTAGCAAATGCA | 23607 |
rs763308138 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47562868 | AGGTTGATGACAACA[A/G]GCAACTGTAGGGGAA | 23607 |
rs763322043 | in-del | -/TA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47598540 | ATAAAGAAATTGTGG[-/TA]TATATATATACCATG | 23607 |
rs763364546 | snp | A/G | 3.31126e-05 | 0.00406881 | missense | CD2AP | GRCh38.p7 | 6:47606218 | TTGCTTCATCTCACT[A/G]CAAATAGACCAAAGA | 23607 |
rs763372452 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47558492 | ATTATATTGAGATAT[A/G]TTCCATCAATACCTA | 23607 |
rs763406185 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47511804 | TTTGAAAATAAGCTT[C/T]CTATTGGGACATTAA | 23607 |
rs763444448 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47607141 | TGACAGGATCTCATT[C/G]TTTTTTGTGACTGAA | 23607 |
rs763463824 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47600868 | TTTAACTCTGGAAAC[A/G]AAAAAGTTATTGCAA | 23607 |
rs763497318 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47608234 | TTTTAATTGAATAAA[A/C]TAAATATTACATATT | 23607 |
rs763501713 | snp | A/T | 2.78122e-05 | 0.00372898 | intron-variant | CD2AP | GRCh38.p7 | 6:47554776 | ATTCAGGTAGACTAT[A/T]TTTTAAAATTTTTAA | 23607 |
rs763590034 | in-del | -/TT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47489978 | AGACTTTTTTTTTTT[-/TT]TTTTTTTTTTTTAAA | 23607 |
rs763590072 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47598474 | TATAGCAGCACAATT[C/T]GCAATTGCAAAGTAT | 23607 |
rs763594204 | snp | G/T | 4.05605e-05 | 0.00450318 | intron-variant | CD2AP | GRCh38.p7 | 6:47554793 | TTTAAAATTTTTAAT[G/T]GATTTAAATAAACTT | 23607 |
rs763610831 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47488204 | TTTGGCAGAGAGAGA[C/T]ATTTCTGTATGAGTC | 23607 |
rs763617362 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47574550 | GTTTTTTGCCTTTTA[A/G]AGCTAAAATTATATA | 23607 |
rs763639814 | snp | C/T | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625307 | AATTTACCTAATAGA[C/T]CAAACTAACTCATGG | 23607 |
rs763647677 | snp | A/G | 6.62274e-05 | 0.00575407 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47606241 | ACCAAAGATGCCTGG[A/G]AGAAGGTTGCCGGGC | 23607 |
rs763650975 | in-del | -/TG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47565556 | ATCTTAAACCTAAGA[-/TG]CCCAAAATTGATCCT | 23607 |
rs763684589 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47600298 | TTTACTGTGATATTC[C/T]TTTAAGAAATCTTAA | 23607 |
rs763690363 | snp | C/G | 1.6476e-05 | 0.00287014 | missense | CD2AP | GRCh38.p7 | 6:47574102 | TCACCTATACCTTCT[C/G]TGGGAAATGTGAGTG | 23607 |
rs763714608 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47621348 | GGTATATCACATTTA[G/T]TGACTTGTGTATGTT | 23607 |
rs763725659 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47504087 | TTCTGCCAGAAAACA[A/G]TCTTTAGGGCTCTTA | 23607 |
rs763725758 | snp | C/T | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520336 | TAAGCTTTATTTTCC[C/T]AAAGAGGAAATCTAT | 23607 |
rs763742173 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47507282 | CTTCAAAGTCATCCT[G/T]TAGTGTTGTGATCTG | 23607 |
rs763743863 | snp | C/T | 1.65206e-05 | 0.00287403 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47595904 | TTCTAAACCAGCAGC[C/T]CCACAAGTCCCACCC | 23607 |
rs763759389 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47498864 | CTGATATCTTTCATC[C/T]AAGTATTTTAGTGTG | 23607 |
rs763786231 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47596630 | TGGTATTCTTTGTGT[A/G]TATATGCCACATTTT | 23607 |
rs763800473 | snp | C/T | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521875 | ACAAAATTAGCTGGG[C/T]TTGGTGGTGCATGCC | 23607 |
rs763824742 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47532445 | CATATCAAGTTAAAA[C/T]TGTTAATTTTAATAT | 23607 |
rs763826786 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47504265 | TTATGAGCTCTTCTA[C/G]GAAGGTTAGAGTATG | 23607 |
rs763829568 | snp | C/G | 1.66043e-05 | 0.00288129 | missense | CD2AP | GRCh38.p7 | 6:47533646 | TGACAGTTTGCCCAT[C/G]AAACGGGAAAGGCAT | 23607 |
rs763846209 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47547295 | CCTCTGCTGCCTTCA[A/G]GAGACTCACTTAACA | 23607 |
rs763872139 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47538385 | TAGCTGGGATTACAG[A/G]CGTGCACCACCATGC | 23607 |
rs763886646 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47576457 | GTAACTGTAAATGGA[A/G]ACTTTGTTTAACAGT | 23607 |
rs763910220 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47523993 | GCTTTAAAGACTGTT[G/T]CCTATAAAACAAATC | 23607 |
rs763934125 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47548496 | CAATCCTCCTTGATT[A/G]AATCAGGAAGAATTA | 23607 |
rs763969170 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47561797 | TTATTTATGTATTTA[C/T]TGAGACGGAGTCTCG | 23607 |
rs763973953 | snp | G/T | 1.64898e-05 | 0.00287135 | missense | CD2AP | GRCh38.p7 | 6:47609285 | TTGTGCATTGTAGAA[G/T]CACTGAAAAAGGATC | 23607 |
rs764005955 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47547675 | CCCTGGAACAAATGG[A/T]GTTAACAAATACTTA | 23607 |
rs764009495 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47621188 | TGTGGGTTTGTCATA[A/G]ATAGCTTTTATTACA | 23607 |
rs764012977 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47586880 | AGTTTTAGGGTAGAT[A/G]TGAGAATTTTTTTGT | 23607 |
rs764067949 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47610891 | GTCCTGATTTTCATA[G/T]GCATATTGCCTGTAG | 23607 |
rs764073537 | snp | A/G | 1.65203e-05 | 0.002874 | missense | CD2AP | GRCh38.p7 | 6:47577011 | TTCTTTATTTCAGCT[A/G]AAGAATATTGTAGAA | 23607 |
rs764116957 | in-del | -/GCTTAGTA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47511128 | CAGGGAAAAATAGTA[-/GCTTAGTA]GCTTTTAATGGAGAA | 23607 |
rs764118747 | snp | A/T | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626054 | TAGAAATTATCCTCC[A/T]GCTTTCTCACCTGAA | 23607 |
rs764126956 | snp | G/T | 4.97459e-05 | 0.00498703 | intron-variant | CD2AP | GRCh38.p7 | 6:47576610 | AATTAAAGGTATGTT[G/T]TTGAATAAAGCTTTC | 23607 |
rs764127386 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47527200 | TCATCAGAAATCCTA[C/T]GTGTGGTAGGCATAA | 23607 |
rs764138809 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47556449 | TTGCCCAGACTAGGA[A/G]CGATTCTCCTGCCTC | 23607 |
rs764142200 | in-del | -/TTC | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476572 | GTTTAGGTGAGTATA[-/TTC]AACTTTTTTCTTTTA | 23607 |
rs764144193 | snp | A/G | 0.000115738 | 0.00760628 | missense | CD2AP | GRCh38.p7 | 6:47503435 | TTCCCTGACAATTTC[A/G]TTAAGGTAAGTATTT | 23607 |
rs764151220 | snp | A/G | 1.69278e-05 | 0.00290923 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624260 | TTCATAATGTTCCAG[A/G]GATTCAGAAGCAACG | 23607 |
rs764180278 | snp | C/G | 1.69398e-05 | 0.00291026 | missense | CD2AP | GRCh38.p7 | 6:47599426 | ATTCACTTACAGTAA[C/G]GACCTCCAAAGAAAC | 23607 |
rs764213007 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47607173 | AGTAGTCCATTGTCT[A/G]TAGTTACCACATTTT | 23607 |
rs764233188 | snp | G/T | 8.43747e-05 | 0.00649463 | missense | CD2AP | GRCh38.p7 | 6:47599314 | AGGATTAATGGGGAA[G/T]TTTCTAGCATTTCAT | 23607 |
rs764246951 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47535721 | TCTGAAACTGCTTGG[A/G]GACTGGGGGACAAAT | 23607 |
rs764268075 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47481589 | GACCTCATGTGATCT[G/T]CCCGCTTTGGCCTCC | 23607 |
rs764313576 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47509215 | ACAATATTTATTAAA[C/T]TTGCTGTCTGACAAG | 23607 |
rs764348589 | in-del | -/TTTTTTTTTTT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47489968 | TTTCTCTAAAGAGAC[-/TTTTTTTTTTT]TTTTTTTTTTTTAAA | 23607 |
rs764356687 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47500136 | CCAGCATTCATCCAT[A/G]ATAGCTGTACTAGTT | 23607 |
rs764356828 | in-del | -/TTAGTCT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47496328 | TTGCTAAGTCACCCA[-/TTAGTCT]GAATGTTGCTTCTTT | 23607 |
rs764364373 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47568368 | ATATTTGGTAGTCAG[C/T]TGTCTATGGGTCTGA | 23607 |
rs764366415 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47584607 | AGCACTCACTCTCTA[G/T]TCCCTAAATATGTCA | 23607 |
rs764380174 | in-del | -/GGTGAAA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47541045 | TTTACCGTGAGGTCT[-/GGTGAAA]GGTGAAATGTGAAAA | 23607 |
rs764418107 | in-del | -/A | 4.73541e-05 | 0.00486568 | intron-variant | CD2AP | GRCh38.p7 | 6:47533555 | TTGAGGATTTAATAT[-/A]AAAAATATAACTTAA | 23607 |
rs764423475 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47592983 | CAGAAGTACGAGAGG[A/G]CAGGACTTGAGATTG | 23607 |
rs764430418 | snp | A/C/G | 3.29588e-05 | 0.00405938 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47574140 | ATCTGGATCAGTTAC[A/C/G]CAGCCAAAGAAAATT | 23607 |
rs764435277 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47579804 | TGTATTTTTATTTAA[A/T]GTTGTTGAAAAGCTC | 23607 |
rs764441302 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47542295 | TGGTGATAGGCTACT[C/G]ATGGAGTGTAGACAC | 23607 |
rs764477717 | snp | A/C | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476524 | ATTTGTTACCTAAAA[A/C]AGGCACATGTTCCAT | 23607 |
rs764500226 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47578439 | TGGTGTTGCAAACTC[C/G]TGGCGTCAGGCAATC | 23607 |
rs764503916 | snp | A/T | 1.71402e-05 | 0.00292742 | splice-acceptor-variant | CD2AP | GRCh38.p7 | 6:47624184 | TATGTTTTTTGTTTT[A/T]GATGGAAATAGAGAA | 23607 |
rs764505470 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47495395 | CCAGATAGGGGCATG[C/G]AGTGATTCTTCAGAG | 23607 |
rs764528062 | snp | A/T | 1.65291e-05 | 0.00287476 | intron-variant | CD2AP | GRCh38.p7 | 6:47554605 | TGACGATTTTCACTT[A/T]ACAGAAGTTGTTTTT | 23607 |
rs764548832 | snp | C/T | 1.65179e-05 | 0.00287379 | intron-variant | CD2AP | GRCh38.p7 | 6:47580915 | GGTATGTAAGAAGCA[C/T]ATTATTCAGTTTGCT | 23607 |
rs764560504 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47513845 | TCAAGTAATTATACC[A/G]ATTTAAAAACGTCTG | 23607 |
rs764581347 | snp | A/G | 1.64904e-05 | 0.00287139 | missense | CD2AP | GRCh38.p7 | 6:47544644 | GTTCTTTTTGAGTAC[A/G]TTCCACAAAATGAGG | 23607 |
rs764600458 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47484815 | TGATTCAGCGTCCAG[A/T]TAATTCCAAGGGAGT | 23607 |
rs764609532 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47577545 | CTGAAACTCTTTTTA[C/T]TCTGGAAAATGATGT | 23607 |
rs764624662 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47591776 | TTTTGTTAGCATACA[G/T]TTTAGACATTTTTGT | 23607 |
rs764649544 | snp | A/T | 3.30327e-05 | 0.0040639 | missense | CD2AP | GRCh38.p7 | 6:47608001 | GAAGCCATCTGAATT[A/T]AAAAAAGATACATGC | 23607 |
rs764692967 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47543950 | GATCATCTACCCATA[A/G]CTGCTTAATGATTCA | 23607 |
rs764713267 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47586383 | ATAGAAAAAAAGTGA[A/G]CAGAATATTGGTTAC | 23607 |
rs764733310 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47587398 | GTTATTTCATGGGAT[A/G]TTTTCTCAAATGTTT | 23607 |
rs764740952 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47565779 | CGCTATCCTGGTATA[A/T]GTTATCTTTTGCTGT | 23607 |
rs764744388 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47601142 | CTAGTAAAAATAATA[C/T]ATGTAATAATTTCAA | 23607 |
rs764746084 | in-del | -/AAA/AAAA/AAAAAAAAAAAAAAAAAAAAA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47609516 | CCCCATCTTTGCAAA[lengthTooLong]AAAAAAAAAAAAAAA | 23607 |
rs764768643 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47503994 | ACTTTTTGTGTTTCA[A/G]CATTATAGCAGTTAT | 23607 |
rs764782695 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47592950 | ATCATGGGAATCCCC[A/G]ATTTATAGCCAATTG | 23607 |
rs764827249 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47600256 | AGCACTATCACATAA[A/G]TCAAAGGAGAACTCT | 23607 |
rs764844009 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47622580 | TCAGATCCAGGTGAA[A/G]TTGGAAACTTCTGCA | 23607 |
rs764865450 | in-del | -/TTTG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47495794 | TGAGTATTTTAAAAA[-/TTTG]TTTGTTCTTTCTCCC | 23607 |
rs764883315 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47518973 | CCTCTTGGTGTTCCA[A/G]TTCAGTTGTTTTATT | 23607 |
rs764897927 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47552665 | CTCCTAAACCTAACT[C/T]CTCAGTTGTTGCCAG | 23607 |
rs764906767 | snp | C/T | 1.64765e-05 | 0.00287019 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47574116 | TCTGGGAAATGTGAG[C/T]GAAACTGCATCTGGA | 23607 |
rs764910304 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47480027 | TTGGACATTGGAATA[C/T]CTATTTTGATTGTCC | 23607 |
rs764947469 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47496496 | AAGGGAAATAAAATA[A/G]ATTTTCTTTGAGTCA | 23607 |
rs764965131 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47499356 | TCTGTGTATACATAC[A/G]TGTATACATATATCT | 23607 |
rs764972261 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47616961 | TCCTCTTCCTTCTTT[C/T]TTTACTTTTTTAATT | 23607 |
rs764983051 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47513667 | TAAGTATTACATATT[G/T]TTTGGATATTTAGGA | 23607 |
rs765012781 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47505892 | GGGCGGCTGGCCGGG[C/T]GGGGGGCTGACCCCC | 23607 |
rs765021913 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47616128 | ATGAAGTCTTGCTCT[G/T]TTACCCAGGCTGGAG | 23607 |
rs765057469 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47611191 | GTTTCAACATCAATA[C/T]GAATTAATCTAAACA | 23607 |
rs765069980 | in-del | -/CTAAAA/CTAAAATCTAATTCACAAAATACTG | 1.64972e-05 | 0.00287199 | cds-indel, frameshift-variant | CD2AP | GRCh38.p7 | 6:47503420 | GGAGAAGAGGAATGT[lengthTooLong]TCCCTGACAATTTCG | 23607 |
rs765090445 | snp | G/T | 1.6507e-05 | 0.00287284 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47596015 | AGTTCCTCCACCACC[G/T]CCTATAGCCAAGTAA | 23607 |
rs765111506 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47526078 | CTCTTTTGGTAAAAG[C/T]GAATGAAGGGCAGAG | 23607 |
rs765214329 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47525284 | TGATTATGCTTCTGT[A/G]AAGTAGGAGATACTA | 23607 |
rs765258162 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47481408 | TGGAGTGCTGTGGTG[C/T]GATCTCGGCTCACCG | 23607 |
rs765258692 | snp | C/T | 3.30251e-05 | 0.00406343 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47577037 | TAGAACATTATTTGC[C/T]TATGAAGGTACTAAT | 23607 |
rs765259118 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47549547 | AAAACTACAAAAACC[C/T]GCTGAAAGAAATAGA | 23607 |
rs765303993 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47568173 | GCAGAGATAGGATAT[A/T]GGGAGATGATGATGT | 23607 |
rs765312040 | snp | A/T | 0.000232875 | 0.0107881 | missense | CD2AP | GRCh38.p7 | 6:47606186 | TAAATTTTGATGACA[A/T]AGCTTCCTCAGAAAA | 23607 |
rs765350094 | in-del | -/ACAC/ACACAC | | | intron-variant | CD2AP | GRCh38.p7 | 6:47566321 | TATATATATATATAT[-/ACAC/ACACAC]ATACACATACACATA | 23607 |
rs765352087 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47620133 | TTCATGAAATCCTTG[C/T]CTGTGCCAATAACTA | 23607 |
rs765373720 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47514118 | TCTTCCTTCTGCTTA[C/T]GTATTCCTCGTAAAT | 23607 |
rs765430650 | in-del | -/T/TTT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47573484 | TTGACATGCTGTGTG[-/T/TTT]TTTTTTTTTTTTTTT | 23607 |
rs765447278 | snp | A/G | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520621 | GTGGTGGTTGGGGGC[A/G]AAAGTGGGGTCTATG | 23607 |
rs765461264 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47581817 | GAACTGAGACCACAG[A/G]GTAGGGTAATAGTGG | 23607 |
rs765462286 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47607024 | CTATCTCCATTAGTT[A/C]AGTTGTTTTAATTTT | 23607 |
rs765488088 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47514474 | TAACTTTGATTCAGT[A/G]TCAATGTCTTGGCTA | 23607 |
rs765588654 | in-del | -/TC | 2.23481e-05 | 0.00334269 | intron-variant | CD2AP | GRCh38.p7 | 6:47606130 | TTAAAAAGGTACAGT[-/TC]TCTTAGTAAATAATG | 23607 |
rs765627691 | snp | A/G | 3.48329e-05 | 0.00417316 | intron-variant | CD2AP | GRCh38.p7 | 6:47599457 | AGGTAAGTCAGCATG[A/G]ACAGCGGTGGTGCAT | 23607 |
rs765668592 | snp | A/T | 1.67091e-05 | 0.00289038 | missense | CD2AP | GRCh38.p7 | 6:47554747 | TGATGGTGAAACTCA[A/T]GAAGCCCAGGACGAT | 23607 |
rs765677803 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47554874 | TTTTGAACTTTGAGT[C/T]AGCTTCAATTAGTCT | 23607 |
rs765702919 | snp | A/G | 6.60458e-05 | 0.00574618 | missense | CD2AP | GRCh38.p7 | 6:47577039 | GAACATTATTTGCCT[A/G]TGAAGGTACTAATGA | 23607 |
rs765703913 | in-del | -/G | 1.67892e-05 | 0.0028973 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624230 | CCTGTCTTCTTGAGT[-/G]GTGTGGACCTGGTGT | 23607 |
rs765716247 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47582192 | TATGTATTTAACAAT[G/T]CTTGGAGTTTTCTGG | 23607 |
rs765717774 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47569427 | TTCTATAGAAAAGGA[C/G]TAATGTTACGAATAA | 23607 |
rs765761772 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47539937 | TAATCCCAGCACTTT[A/G]GGAGGCTGAGGTGGG | 23607 |
rs765765778 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47556312 | TATGAATGAGAACAT[A/G]TAGTGTTTGCTTTTC | 23607 |
rs765823737 | snp | C/T | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521786 | TTTGGGAGGCTGAGG[C/T]GGGCAGGTCACCTGA | 23607 |
rs765851455 | in-del | -/TTTTTT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47553516 | CACACCTAGTGAATT[-/TTTTTT]TTTTTTTTTTTTTTT | 23607 |
rs765893069 | snp | C/T | 1.66524e-05 | 0.00288547 | intron-variant | CD2AP | GRCh38.p7 | 6:47580824 | TAACTATATTTGATA[C/T]GAAACTGGTCAGCCG | 23607 |
rs765919127 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497554 | TAGTTGGGACTGTAG[A/G]TGCGTTATCATTACT | 23607 |
rs765919738 | in-del | -/GAGGGAGAGGGAGAGGGA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47506795 | GGGGAGAGGGAGACG[-/GAGGGAGAGGGAGAGGGA]GAGGGAGAGGGAGAG | 23607 |
rs765920915 | in-del | -/CAAA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47609513 | AAAACCCCATCTTTG[-/CAAA]AAAAAAAAAAAAAAA | 23607 |
rs765923743 | snp | C/T | 0.000101051 | 0.00710741 | intron-variant | CD2AP | GRCh38.p7 | 6:47609073 | TTAAAATCTTTCGAA[C/T]GTAAATATAATATTA | 23607 |
rs765928457 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47493797 | TGGAAAATTTCTTTT[G/T]ACCTCTCTTCAAGCT | 23607 |
rs765940593 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47549842 | CACCAAAACAGCATG[C/G]TACTGGTATAAAAAT | 23607 |
rs765942625 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47528893 | ATATTTCTTTGTATA[G/T]CTCAAATGACAGTCT | 23607 |
rs765945407 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47500421 | TGGCTTTATCAGCTG[C/T]GCATCCCCTTTCAGA | 23607 |
rs765959704 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47564447 | CATTACTTTTATAAT[C/T]ATAAAATACTTTGCA | 23607 |
rs765970964 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47613894 | AACTTGCTGCAGCTT[C/G]TACATTAGCACTTGC | 23607 |
rs766019387 | in-del | -/TT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47498265 | ATACTTCAGTGACTT[-/TT]AATTTTTCTTTTTCT | 23607 |
rs766048926 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47565673 | GATTTCTCTTGTACT[A/C]TTCTTTTTAACCTCG | 23607 |
rs766063740 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47571511 | TTTTGTTGAGGATTG[A/T]TCAAAATTCAGGGAA | 23607 |
rs766066395 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47529829 | TTCAGATTGCCTACC[C/T]AGACTCAGAGAGCTT | 23607 |
rs766081735 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47578148 | CACCTAATTTTTCAT[A/G]CAAGGGTGGTGGGTA | 23607 |
rs766106568 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47570524 | TCCTTTTTCCTTTCT[C/T]CTTGCTCCTTATCCT | 23607 |
rs766151466 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47558901 | TCAGAAGGAATGGTA[C/G]CAGCTCCTCTTTGTA | 23607 |
rs766165866 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47551092 | TGCAGTGTATACTCC[C/T]CAGGTGATGGGTGCA | 23607 |
rs766189692 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520731 | GGACTGGTGCTACAG[-/TT]TTTTTTTTTTTTTTT | 23607 |
rs766224620 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47503751 | TAATTTATAAAGCAG[G/T]CTTGCTGTATATATT | 23607 |
rs766246750 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47608800 | GAATATGAAAGATCA[A/G]AGTAATACCTTTATA | 23607 |
rs766248270 | snp | A/G | 3.32745e-05 | 0.00407875 | intron-variant | CD2AP | GRCh38.p7 | 6:47576487 | TATTATCTTTATTCT[A/G]TCTTAAAATAGTTTA | 23607 |
rs766263548 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47586306 | ATGTCCAGTAGAGTG[C/G]AAACTGCAGAAGAAA | 23607 |
rs766268810 | snp | C/T | 8.50955e-05 | 0.00652231 | utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47478238 | TCTCCCCGCGGGAGC[C/T]CCCAGCATGGGTAAG | 23607 |
rs766270873 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47535824 | GAGGTTTTTTCATGA[C/T]CTCTGTCCATAGTAA | 23607 |
rs766276730 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47622509 | CAGCAAGCTCCCAGG[A/G]CCTTTCAGCTGCTTC | 23607 |
rs766277158 | snp | A/G | 1.65362e-05 | 0.00287538 | intron-variant | CD2AP | GRCh38.p7 | 6:47596036 | AGCCAAGTAAGTTTT[A/G]CCTAATTTTAAATTA | 23607 |
rs766277860 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47500381 | TCATTTATAGCTCCC[A/T]TAGGTTCTCTAGGCT | 23607 |
rs766301489 | snp | A/G | 1.65051e-05 | 0.00287267 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47574215 | ACTTCGGACAAGAAC[A/G]TCCAGTAGTGAAACA | 23607 |
rs766323424 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47489038 | CTTGTAGTTGTCTAT[A/G]TAACTTAATTATGTT | 23607 |
rs766390153 | in-del | -/G | 1.88653e-05 | 0.0030712 | intron-variant | CD2AP | GRCh38.p7 | 6:47624146 | AAACTACTAAACTAA[-/G]GATATTTTATGTTTG | 23607 |
rs766393140 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47501490 | GCTGAGAGAATCTTC[G/T]CCTGTAAAGTACAGG | 23607 |
rs766411348 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47617105 | AAGTAGCTGAGACTA[C/T]AGGCATGCACTTTCA | 23607 |
rs766433012 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47580245 | TATGTTTGTACATTA[C/T]GGCTTATCAATTATT | 23607 |
rs766436212 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47621608 | TTGTGGAATAGTGTC[A/G]AAAGGATTGGTACCC | 23607 |
rs766456040 | snp | C/G | 5.1079e-05 | 0.00505341 | intron-variant | CD2AP | GRCh38.p7 | 6:47579369 | ATTGTCTTAATTATT[C/G]TATTTTGCTTTTTAG | 23607 |
rs766470799 | snp | A/G | 1.8582e-05 | 0.00304806 | intron-variant | CD2AP | GRCh38.p7 | 6:47612460 | TTAACAGTAATAAGT[A/G]CTTTGTTTTTAGGAA | 23607 |
rs766488911 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47618815 | GCAAAGTGAGCTGTT[-/A]ACTTGGCCTCTCACT | 23607 |
rs766574639 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47525909 | TGAAGTATGAAACTC[A/G]AGTTTTTCAGAGTTT | 23607 |
rs766588935 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47513561 | TTTTTTCTCCCAGAA[C/T]GCATGGTGTTTAAGA | 23607 |
rs766617305 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47546973 | TTCAGACAAACAAAT[A/G]CTGAGAGAATTCACT | 23607 |
rs766661745 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47593550 | TAAGCACTTGACAAG[A/T]TGTTTAATATCATTA | 23607 |
rs766697082 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47568145 | TTGGCTTTGTAAGAT[A/G]GAGATGTCATTTGCA | 23607 |
rs766701858 | in-del | -/CACT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47583659 | CACAGTTTATTAATC[-/CACT]CACTCACTGAGGGAC | 23607 |
rs766704769 | in-del | -/CA/CCCT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47527112 | TAAAAGACTCCCCCC[-/CA/CCCT]CGATTGAAAAATATT | 23607 |
rs766725000 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47507508 | GATCTTGGCTCACTG[C/T]AACCTCTGCCTCCCA | 23607 |
rs766731019 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47553109 | TGATTTTTTCTTTAA[A/G]TGTTTTATTGAAGAA | 23607 |
rs766737753 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47553513 | ACCACACCTAGTGAA[-/T]TTTTTTTTTTTTTTT | 23607 |
rs766743624 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47545794 | TCTCAGGAAGCCACA[A/T]CCCTAGGAAAAGAGG | 23607 |
rs766777357 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47479901 | TTCTAATTTTTTTTT[A/G]GAAGTGTGGAAATCA | 23607 |
rs766777830 | in-del | -/TAGCCATG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47532956 | ACATGTCTTATTTTA[-/TAGCCATG]ACTTAGATCAGGGGC | 23607 |
rs766787969 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47519429 | AGTTTGGCATTGTGA[C/G]AGGAGTACGGCCTTT | 23607 |
rs766800591 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47598898 | TTTCTCAAAAACCTG[C/T]TGAAATAAAAAATAA | 23607 |
rs766850860 | snp | C/T | 1.70717e-05 | 0.00292157 | intron-variant | CD2AP | GRCh38.p7 | 6:47606317 | CTACAGTATATTTAG[C/T]AAATGCAGAGTCCAT | 23607 |
rs766856654 | in-del | -/A | 0.004257 | 0.0459388 | intron-variant | CD2AP | GRCh38.p7 | 6:47599474 | AGCGGTGGTGCATTT[-/A]AAAAAAAAAAATTGT | 23607 |
rs766903995 | snp | A/G | 1.65542e-05 | 0.00287695 | missense | CD2AP | GRCh38.p7 | 6:47606221 | CTTCATCTCACTGCA[A/G]ATAGACCAAAGATGC | 23607 |
rs766906445 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47569411 | TCTGACTTTTGATAT[C/T]TTCTATAGAAAAGGA | 23607 |
rs766910368 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47604941 | TAGTTGTTATAAAAT[G/T]CATATTACCGAACAG | 23607 |
rs766919155 | snp | C/T | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520504 | TGTCCATATGGCCTC[C/T]GCTGACAGCAGGGGG | 23607 |
rs766920131 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47558133 | CCCTCTGTTTGTCTT[C/T]TATTGGTGTATAGGA | 23607 |
rs766938034 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47501220 | AGCCAGACCCCATCT[C/G]TATTTAAAAAATAAA | 23607 |
rs766980577 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47481284 | ATAAGGCGGTGAACT[G/T]TTTAGTTTATTTTAT | 23607 |
rs766983546 | snp | A/T | 2.75168e-05 | 0.00370913 | intron-variant | CD2AP | GRCh38.p7 | 6:47554780 | AGGTAGACTATTTTT[A/T]AAAATTTTTAATTGA | 23607 |
rs767002807 | snp | A/G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47504102 | ATCTTTAGGGCTCTT[A/G/T]TCAATTACAAACTTA | 23607 |
rs767008547 | snp | G/T | 1.70988e-05 | 0.00292389 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624275 | GGATTCAGAAGCAAC[G/T]CTATGAACTTCAGCT | 23607 |
rs767011905 | snp | G/T | | | downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47627473 | GCATTTTACAGTGAT[G/T]GATATGATAAAAATT | 23607 |
rs767033792 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47575487 | GTCAGGCTTGCTTTG[A/G]TCACTGATCCAGGAA | 23607 |
rs767046879 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47595198 | TTGTCTTTATTGACA[C/T]AGTATAAAATTGTCA | 23607 |
rs767065306 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47613729 | ACCTAACAAGAGTCA[A/G]CCTGTCCTTTGAAGC | 23607 |
rs767092732 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47528422 | TCAAGTGATCTGCCA[A/G]CCTCAGCCTCCCAAA | 23607 |
rs767098117 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47618150 | ATGGCAAAACCTTGT[C/T]TCTACTAAAAAATAT | 23607 |
rs767106979 | in-del | -/TATT | | | intron-variant, downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47603941 | ACATGTCTGTCTGTC[-/TATT]TATTCTAACCCTTTT | 23607 |
rs767117378 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47562982 | CAAAGAATCTTACGC[C/T]CAGTATGTCATCGAA | 23607 |
rs767135554 | snp | C/T | 1.65403e-05 | 0.00287574 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47609167 | TGCTTCTAAAGCAAA[C/T]ACAACTGCTTTCCTG | 23607 |
rs767173291 | snp | C/G | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626088 | CTATTGAAGTGATCC[C/G]TGGTCATCCTAATAA | 23607 |
rs767174046 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47514923 | CAGGAGTGGTGGCAC[A/G]CACCTGCAATCCCAG | 23607 |
rs767203625 | snp | C/G/T | 3.30138e-05 | 0.00406276 | missense, synonymous-codon | CD2AP | GRCh38.p7 | 6:47503428 | AGGAATGTTCCCTGA[C/G/T]AATTTCGTTAAGGTA | 23607 |
rs767219776 | in-del | -/AAAA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47504845 | CAATCGCATTATATT[-/AAAA]AAAGCAATGTGGATA | 23607 |
rs767222363 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47491804 | CAGATATCCTTTTTG[A/T]TTAAATACTGATTTT | 23607 |
rs767222807 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47616810 | CCCTTGCATCTTAGG[C/T]TAGGTTTACTGATGC | 23607 |
rs767232232 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47545218 | ATGTGGAGGCTCACA[C/T]TGTGAACTTTTGCTC | 23607 |
rs767246659 | snp | G/T | 1.65699e-05 | 0.00287831 | missense, intron-variant | CD2AP | GRCh38.p7 | 6:47576602 | GAAGGTAAAATTAAA[G/T]GTATGTTTTTGAATA | 23607 |
rs767268117 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47526689 | CCTGAACCTGTCCTC[G/T]ATCACATTTGGTCAG | 23607 |
rs767287076 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47599831 | TTATATTTCATAGGA[A/C]TTTAAATTTCTCCTC | 23607 |
rs767294971 | in-del | -/GTGATG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47519361 | CAAAGTAGGCTGCAT[-/GTGATG]GTGATGGTTTGGGTT | 23607 |
rs767323060 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47553591 | GGCTGGTCTCAAACT[C/G]CTGACCTCAGGTGAT | 23607 |
rs767353229 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47535795 | GTGCTGAGGGAGAAT[A/T]TTTAGGCCCACGGGA | 23607 |
rs767366553 | in-del | -/GGGA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47500170 | TAAGCTATTTTTTAT[-/GGGA]TTTTTTGTAGATTAA | 23607 |
rs767370373 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47501378 | CTGGCACCTGCTCAA[A/C]TGTAGTTGGCATTTA | 23607 |
rs767378264 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47519905 | AAAGAGGAAAACAGT[A/T]AAAATGAGAAAATGT | 23607 |
rs767386348 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47606074 | TGGTACTCTTTTTAA[-/T]TTTATAGTTTGTCCA | 23607 |
rs767391772 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47598518 | ATGCCCATGAATCAA[C/T]GAGTGAATAAAGAAA | 23607 |
rs767423467 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47569791 | TCTGCAGGCTAGTCA[C/T]CAGGAGTCAAGGTAT | 23607 |
rs767423641 | snp | A/G | 1.6534e-05 | 0.00287519 | missense | CD2AP | GRCh38.p7 | 6:47503286 | CTTTTTTAGTTGACT[A/G]TATTGTGGAGTATGA | 23607 |
rs767431919 | snp | A/G | 1.66114e-05 | 0.00288192 | intron-variant | CD2AP | GRCh38.p7 | 6:47576502 | ATCTTAAAATAGTTT[A/G]TGCCATTTTTTTCTA | 23607 |
rs767476189 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47534652 | GAGCCGAGATCTGCC[A/T]TTGCACTCCAGTCTC | 23607 |
rs767494418 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47598314 | GTGGGAATGTAAACT[A/G]GTAGAACCACTATGG | 23607 |
rs767543228 | snp | A/G | 1.80185e-05 | 0.00300149 | intron-variant | CD2AP | GRCh38.p7 | 6:47599251 | ATCACAATTTAAAAA[A/G]AAGTCGTGTTTCATA | 23607 |
rs767549155 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47544198 | TGCTTCTTTCTATAG[C/T]CGTAAAAGTACTAAT | 23607 |
rs767564558 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47500241 | TTAGCATTTTATCTC[A/G]TTGAATTACTGTGGT | 23607 |
rs767576034 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47591862 | AGACAGGGTCTCACT[C/T]TGTTGCCCAGGCTGG | 23607 |
rs767590894 | in-del | -/TTTTTTT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47489167 | TGCACTCAACTAGTT[-/TTTTTTT]TTTTTTTTTTTTTTG | 23607 |
rs767594523 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47593155 | ATCCCCACACATTTG[A/G]TGTCTCAGAGTGTTA | 23607 |
rs767664805 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47494202 | AGGATTTATATTTAT[C/T]TGCCTAGGAGTTGGA | 23607 |
rs767670681 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47558735 | TTGCCAGTATTTTAT[G/T]GAGGATTTTCGCATT | 23607 |
rs767710155 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47586603 | ATACCTTTTGGGAAT[A/G]GGTCAAAATTAAAAC | 23607 |
rs767758079 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47599284 | AGTGATTTTTGCGTG[-/T]TTTTTTCTTATTTCA | 23607 |
rs767758810 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47560514 | TGACATTGACATTTT[C/T]GAAGAGTTTAGGCTG | 23607 |
rs767759266 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47484193 | GTAGAGACATTTATT[A/T]TGTCTCTTAAACAGA | 23607 |
rs767777599 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47523363 | GACTGTAGTAATCAT[C/T]TCACTATCTACACAT | 23607 |
rs767823886 | snp | A/G | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521419 | TAGCTGGGCGTGGTG[A/G]CGGGCGCCTGTAATT | 23607 |
rs767835978 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47567182 | TTTGCTGCTATCTTC[A/G]TCTAATTTTCTTTTA | 23607 |
rs767848102 | snp | A/C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47530144 | TTAGCTACACTTCCT[A/C/G]TGTTAGGCATTTGGT | 23607 |
rs767908402 | snp | A/G | 1.65124e-05 | 0.00287331 | missense | CD2AP | GRCh38.p7 | 6:47544611 | CTTTCTTTAGAGACC[A/G]AGAAGCGTCAGTGTA | 23607 |
rs767943739 | snp | C/G | 1.65015e-05 | 0.00287237 | missense | CD2AP | GRCh38.p7 | 6:47607984 | GAAGACAGTGCCAAC[C/G]TGAAGCCATCTGAAT | 23607 |
rs767969354 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47579965 | AGTCATTCATCAGTG[A/G]TCTTTTGCCTTCCTA | 23607 |
rs767992435 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47551699 | GAATTCAGATGGGGT[A/G]TAGCCCAAATGGCTT | 23607 |
rs767998598 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47545569 | ATAGTGCATTAAACA[A/G]CCAGAGCTAAGGACC | 23607 |
rs768001955 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47535496 | TCTACTTTTGGATTA[C/T]ATCATCCTTTGATTA | 23607 |
rs768009858 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47548373 | AAAGCAGGAGATATT[-/A]ACAGTTGACACCACA | 23607 |
rs768016875 | snp | C/T | 1.65685e-05 | 0.00287819 | intron-variant | CD2AP | GRCh38.p7 | 6:47579382 | TTCTATTTTGCTTTT[C/T]AGGAGACTGGAGAAG | 23607 |
rs768055057 | snp | A/C/T | 0.00017282 | 0.00929439 | utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47478229 | ACGTCGGCTTCTCCC[A/C/T]GCGGGAGCCCCCAGC | 23607 |
rs768081024 | in-del | -/AAGT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47575577 | AGTTGGGGAAAACTA[-/AAGT]AAGTATTTTAGAAGA | 23607 |
rs768081296 | snp | C/G | 1.64988e-05 | 0.00287213 | missense | CD2AP | GRCh38.p7 | 6:47595980 | TCTGGAACAGTGTAC[C/G]CAAAGCGACCTGAAA | 23607 |
rs768095607 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47555817 | TAATTTTTTTTTTAA[C/T]GTGAAAGGGCTGTTT | 23607 |
rs768104092 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47508459 | GAGAATTAGGGCCTT[A/G]CTCTAGATGAGGCTT | 23607 |
rs768186886 | snp | C/G | 0.000214381 | 0.0103511 | intron-variant | CD2AP | GRCh38.p7 | 6:47599267 | AAGTCGTGTTTCATA[C/G]TAGTGATTTTTGCGT | 23607 |
rs768196661 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47478424 | ACCTTGCTCTTCTCA[A/C]GGAGAAACTGGTGGG | 23607 |
rs768227130 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47620685 | CCATCCACGAGCGTG[A/G]GATGTGTTTTCATTT | 23607 |
rs768227169 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47604867 | TAATGAATCAGCTTA[G/T]TTGATACAAGTGAGA | 23607 |
rs768239224 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47583839 | GTAGGCGCAACTGCC[A/G]AACTTCTTCCAATGT | 23607 |
rs768264877 | snp | C/G | 1.7949e-05 | 0.00299569 | intron-variant | CD2AP | GRCh38.p7 | 6:47533787 | TTTCCTGCATAATTA[C/G]ATCAAAATAGAAGGA | 23607 |
rs768291148 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47622460 | TCCCTATGGATCCCT[C/G]TGGTGCCAGGCAGGA | 23607 |
rs768293057 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47568020 | TGCTATGGGGATGGA[A/G]AGACACGTGTAGAAT | 23607 |
rs768341965 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47562196 | TATTAGGCTTGAAAG[A/G]ATGAATGCTTAGAAA | 23607 |
rs768383094 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47554592 | TTTTCCCATAGGGTG[A/G]CGATTTTCACTTAAC | 23607 |
rs768393579 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47578954 | GAGCCACCGTACCCG[A/G]CCTCATTTTATCTTT | 23607 |
rs768396110 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47614808 | CTGTGCAGTTAAGCT[A/G]TTTTCATTCTTTCTT | 23607 |
rs768441101 | snp | A/T | 2.62367e-05 | 0.00362183 | intron-variant | CD2AP | GRCh38.p7 | 6:47579351 | AAAAAAAAAAAAAGG[A/T]CTATTGTCTTAATTA | 23607 |
rs768444308 | snp | C/T | 6.64198e-05 | 0.00576242 | missense | CD2AP | GRCh38.p7 | 6:47533728 | GGAGGAATTCAGCCA[C/T]ATCCACAAACCAAAA | 23607 |
rs768446712 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47490738 | GAAGAATATAATACT[A/G]TGTAAAAATTTCCTT | 23607 |
rs768462724 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47577642 | CCCAGTACTACTTGT[A/G]TGTGGGCAGAATCCT | 23607 |
rs768466426 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47481742 | CTTTGTTGTACTGTT[G/T]GGAGAAAATATTTTA | 23607 |
rs768496169 | in-del | -/A | 4.37474e-05 | 0.00467673 | intron-variant | CD2AP | GRCh38.p7 | 6:47609092 | AATATAATATTAAAT[-/A]AAATCAGAAATTTTT | 23607 |
rs768518396 | in-del | -/AA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47549463 | TACAATAGCTGCAAA[-/AA]AAAAAAAAAAAAAAA | 23607 |
rs768558688 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47481651 | GCACCTGGCCTCGTG[C/G]TGGTTTTAATAGACA | 23607 |
rs768585659 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47591205 | TAAAAATATTCATAA[A/G]TAATCTGTGGTGTTA | 23607 |
rs768635862 | snp | A/G | 1.66363e-05 | 0.00288407 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47606271 | CCGTTTCAATGGTGG[A/G]CATTCTGTGAGTTCA | 23607 |
rs768636117 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47493058 | AATTTCATCTATTCA[C/T]ATGCTATAATCATGC | 23607 |
rs768687173 | snp | A/G | 1.72101e-05 | 0.00293338 | splice-acceptor-variant | CD2AP | GRCh38.p7 | 6:47606164 | TATTTTTATTTTCTA[A/G]ATGTTGTAAATTTTG | 23607 |
rs768687953 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47498855 | TTTTCCTGACTGATA[A/T]CTTTCATCCAAGTAT | 23607 |
rs768724203 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47502619 | CTACCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 23607 |
rs768731414 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47528291 | GTGATTCTCATACCT[C/T]ATCCTCCCAAGGAGC | 23607 |
rs768731802 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47543389 | AAGATTGAGAACCAC[C/G]TAGGGATCTTGTTAA | 23607 |
rs768744620 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47570191 | GTGGTTTCTTGTTTC[C/T]GTTTTTCTCCAAACA | 23607 |
rs768797259 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47565199 | TAGGAATGTGGTGAA[C/T]TAATCATCTATTCTG | 23607 |
rs768824467 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47536355 | TATTAATATTAATTT[A/T]AAAAAACCCAAAACC | 23607 |
rs768829951 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47585854 | ATAATATATAGCACA[C/T]TGGATAGAGTTCATA | 23607 |
rs768872740 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47593538 | TAATCATGTCAGTAA[A/G]CACTTGACAAGATGT | 23607 |
rs768878089 | snp | C/T | 1.65296e-05 | 0.00287481 | missense | CD2AP | GRCh38.p7 | 6:47582027 | CTGAACTGATAGCTG[C/T]AGAGAAGAAATATTT | 23607 |
rs768885574 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47550745 | CACATGTTTATAGCA[G/T]CACAGTTCACAATTG | 23607 |
rs768921584 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47570805 | GAATCAAGAAAATTC[A/G]ACCCTAGAGTTCATA | 23607 |
rs768923117 | snp | A/C | 2.22373e-05 | 0.00333439 | intron-variant | CD2AP | GRCh38.p7 | 6:47533570 | AAAAAATATAACTTA[A/C]CTTGCCTCTTTATTT | 23607 |
rs768956910 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47609983 | TTCTGTGAGGTTGAG[G/T]TGGACATTTATAAAA | 23607 |
rs768982225 | snp | C/T | 1.67181e-05 | 0.00289115 | intron-variant | CD2AP | GRCh38.p7 | 6:47595838 | TTGATTGTTAATAAC[C/T]TGTGAAATATTTTAA | 23607 |
rs768999239 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47617673 | ATCCCCACTGTATCT[A/G]TCTTGTTCTGATGCT | 23607 |
rs769052415 | in-del | -/CT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47615755 | GTAACAGCAATGGAG[-/CT]GAAATTTAATTTTAA | 23607 |
rs769062684 | snp | A/G | 3.31098e-05 | 0.00406864 | missense | CD2AP | GRCh38.p7 | 6:47554727 | AAAGAATTAGAGGTA[A/G]CAGATGATGGTGAAA | 23607 |
rs769063268 | in-del | -/TT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47489967 | TTTCTCTAAAGAGAC[-/TT]TTTTTTTTTTTTTTT | 23607 |
rs769125380 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47617657 | TAATCTTTATGTCTT[C/T]ATCCCCACTGTATCT | 23607 |
rs769147718 | snp | C/G/T | 3.43863e-05 | 0.00414634 | intron-variant | CD2AP | GRCh38.p7 | 6:47608079 | CTGGGATTCTTTGTG[C/G/T]ACATCAAACATAGGG | 23607 |
rs769152362 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47582248 | GATAACAATTTACAT[G/T]CATTAAAAAATTAAA | 23607 |
rs769170284 | snp | C/T | 1.66233e-05 | 0.00288295 | intron-variant | CD2AP | GRCh38.p7 | 6:47503261 | ATTTTAGACATTTCG[C/T]TTTTTCCCCCTTTTT | 23607 |
rs769211242 | in-del | -/C | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625207 | ATGGTAATAGGAAAA[-/C]AAAACCCAAAGCTTT | 23607 |
rs769243431 | snp | G/T | 1.64855e-05 | 0.00287097 | missense | CD2AP | GRCh38.p7 | 6:47503404 | GGAAGGAGAACTAAA[G/T]GGGAGAAGAGGAATG | 23607 |
rs769252314 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47603126 | ATACTATAAAAAGTG[A/G]GCCTATATCTAAACT | 23607 |
rs769257536 | snp | A/G | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520197 | ACTGAGACTGGGGAT[A/G]AAGCAGACATCTCTG | 23607 |
rs769257597 | snp | A/G | | | synonymous-codon | CD2AP | GRCh38.p7 | 6:47533727 | TGGAGGAATTCAGCC[A/G]CATCCACAAACCAAA | 23607 |
rs769258633 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47539628 | GTAGTCTTTGATGGA[C/T]TATTTAACTTTTTAT | 23607 |
rs769274818 | snp | C/T | 1.67829e-05 | 0.00289675 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47624224 | AGCTGTCCTGTCTTC[C/T]TGAGTGGTGTGGACC | 23607 |
rs769301839 | in-del | -/ATTT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47615793 | TTTTAATTTAATTTA[-/ATTT]ATTTATTTATTTATT | 23607 |
rs769314023 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47574448 | TTGAATCTAATAAAA[G/T]TAGAATGCTTATTTC | 23607 |
rs769409950 | snp | A/T | 1.65471e-05 | 0.00287633 | missense | CD2AP | GRCh38.p7 | 6:47576582 | AGATAACAAAAACAG[A/T]TACCGAAGGTAAAAT | 23607 |
rs769462235 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47537328 | TGAGTGTGTTGGTTC[A/G]TGGTGGCTCTTTGAC | 23607 |
rs769463446 | snp | G/T | 6.65225e-05 | 0.00576687 | intron-variant | CD2AP | GRCh38.p7 | 6:47574289 | ATTAACTCCACTCAT[G/T]CTCTCATTAAGCATT | 23607 |
rs769463474 | snp | G/T | 1.67668e-05 | 0.00289537 | missense | CD2AP | GRCh38.p7 | 6:47599350 | TTTGAAACTGAGCCA[G/T]TATCAAAACTAAAGC | 23607 |
rs769480805 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47546415 | AGAAATCTAAAAGTT[C/T]AAAAAAAAAATTGGG | 23607 |
rs769502031 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47601413 | TTCCACTTAATTATA[A/C]TACCTTTGGTGTACT | 23607 |
rs769516289 | snp | G/T | 1.7802e-05 | 0.0029834 | intron-variant | CD2AP | GRCh38.p7 | 6:47599270 | TCGTGTTTCATACTA[G/T]TGATTTTTGCGTGTT | 23607 |
rs769519553 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47567023 | CAAGAAGTGGAAACT[C/G]CTGAGATTATTTAAC | 23607 |
rs769534524 | snp | A/G | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626838 | AATCAGAAATGAGAA[A/G]TATTATAATGTAAAG | 23607 |
rs769540401 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47591069 | GCACAAATGTTCAAC[A/C]GCAAAAGAATGGGTA | 23607 |
rs769541044 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47496594 | GAACAAACCACTTTA[A/G]TATTTACTGCTTAAA | 23607 |
rs769564467 | snp | A/G | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625065 | AACTTGTGCCTAGAA[A/G]CTACAGCACATATAA | 23607 |
rs769579179 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47526264 | TGTATGTGTGTGTTT[C/G]TAGTAGTAAGGGATT | 23607 |
rs769583566 | snp | A/G | 1.69235e-05 | 0.00290886 | intron-variant | CD2AP | GRCh38.p7 | 6:47544558 | AAATATACTGTTTTT[A/G]AAAATGATCATTCTT | 23607 |
rs769586575 | snp | A/G | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625096 | AATATGTAAACACCA[A/G]CCTGTTGCTGTACTT | 23607 |
rs769602121 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47552307 | GCCACCCCCATTCTT[C/T]CCCCCCAAGTCCCCA | 23607 |
rs769605207 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47589809 | AAGCTCATGAAAGAG[A/G]AGGTATCCTAGTGAA | 23607 |
rs769616819 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47515214 | ATATGGGGGAGTAAT[A/G]GGATTTAAGACTAAA | 23607 |
rs769627529 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497714 | CTGCAACTGCACCCG[A/G]ACAATTATATTTTGA | 23607 |
rs769628039 | snp | A/G | 3.2987e-05 | 0.00406108 | intron-variant | CD2AP | GRCh38.p7 | 6:47612585 | GAGCATAAACTGGAC[A/G]TGTTTTTCCCAACCC | 23607 |
rs769633907 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47556493 | GTTGGGATTACAGGC[A/G]TGTGCCACCACGCCC | 23607 |
rs769681987 | snp | A/G | 3.31235e-05 | 0.00406948 | missense | CD2AP | GRCh38.p7 | 6:47579478 | ATAAATGAACTTGAT[A/G]AAGACTTTCCAGTAA | 23607 |
rs769731546 | snp | A/C | 1.65941e-05 | 0.00288041 | intron-variant | CD2AP | GRCh38.p7 | 6:47607920 | TGACTTCTAAAAAAT[A/C]ATTTAGCCAACTCAC | 23607 |
rs769745343 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47604599 | TGTGGGTTGTTAATG[C/T]ACACATCAGTGTAAA | 23607 |
rs769755750 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47583133 | CAGTTTTAGGTTCAC[A/G]GCAAAATTGAGCCAA | 23607 |
rs769787808 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47554200 | ACAGACCTGAGCCAC[C/T]GTGCCTGGCCAGGAA | 23607 |
rs769819851 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47499783 | AGTCTTGCTCTGTCG[C/T]AGTGGCACGACCTCG | 23607 |
rs769873567 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47555721 | CAAGATCATACTAAG[A/G]TGTTAGTCTTCCGTG | 23607 |
rs769883915 | in-del | -/GGTAT | 1.65679e-05 | 0.00287814 | intron-variant | CD2AP | GRCh38.p7 | 6:47576602 | GAAGGTAAAATTAAA[-/GGTAT]GTTTTTGAATAAAGC | 23607 |
rs769895259 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47528249 | CTGTGATCTTGGCTC[A/T]CTGCAACCTCCGCCT | 23607 |
rs769899460 | in-del | -/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47597598 | CCAGGAGCAGATGTG[-/C]CCAGGAACTTGACTT | 23607 |
rs769917538 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47515428 | TAATAACACTTTATA[A/T]CTGTATGAATACTTT | 23607 |
rs769932245 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47548398 | ACCACAGAAATACAA[A/G]AGGTCATTCAAGGCT | 23607 |
rs769942368 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47577453 | TTTCTCCTGTCTGTC[A/G]TTTGGAGTGTTGTTT | 23607 |
rs769973989 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47598210 | TGTGATACCACCTCA[A/C]TTCTGCAAGAATGGC | 23607 |
rs770001293 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47598267 | AGATGTTAGCATGGA[-/T]GCAGTGAAAAGGGAA | 23607 |
rs770006770 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47572189 | TGTAAAATTTAACAT[A/T]CAACAACATCAAAAT | 23607 |
rs770034676 | snp | A/G | 1.64953e-05 | 0.00287182 | intron-variant | CD2AP | GRCh38.p7 | 6:47574031 | GTTTTGTGATTCTAG[A/G]TGTCATTCTTCAAAA | 23607 |
rs770102561 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47549458 | GCCTTTTACAATAGC[A/T]GCAAAAAAAAAAAAA | 23607 |
rs770107926 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47613267 | ATTTTTTCCAAATGG[G/T]TTTCAGTTTATTTGC | 23607 |
rs770123305 | snp | A/G | 1.64836e-05 | 0.0028708 | missense | CD2AP | GRCh38.p7 | 6:47574160 | CAAAGAAAATTCGAG[A/G]AATTGGATTTGGAGA | 23607 |
rs770126997 | snp | A/G | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521074 | TTTTTACATATGTAA[A/G]GTCCAGAGCTTTAAA | 23607 |
rs770163493 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47612721 | TGCAACAACATGGAT[G/T]GAACTGGAGGTCATT | 23607 |
rs770175851 | snp | C/T | 9.98801e-05 | 0.00706612 | intron-variant | CD2AP | GRCh38.p7 | 6:47595858 | AAATATTTTAAATCT[C/T]AGATGAAAAATCAAC | 23607 |
rs770181349 | snp | C/T | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476069 | CTTGAATTTACTACC[C/T]ATGTATGTGCTTCCA | 23607 |
rs770217253 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47536304 | AAAGTGGCTCATTGT[A/G]TTGTTACATAGTAGC | 23607 |
rs770237722 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47570673 | ATAGACACTGAGCCA[C/G]GCACTGTTTAAAGCA | 23607 |
rs770244652 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47524241 | AGGTAAACCAGGTAT[C/T]AGGAAAGTTGAGTGC | 23607 |
rs770246041 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47572017 | TTCAGGGGCTCTCTG[C/G]CACATACAGGATGTT | 23607 |
rs770257262 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47500935 | TATATTTTTAGTAGA[A/G]ATGGGGTTTCACCAT | 23607 |
rs770258436 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47608122 | TCTTTAGGACGAATT[A/G]TTTTTTCTGCCAAGA | 23607 |
rs770278392 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47487935 | CAACCTAACAATACA[A/T]AATTTAAATATATTG | 23607 |
rs770290719 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47496394 | TCTTTGTCTTTCACT[G/T]TTTGCAGTTTAATAT | 23607 |
rs770319224 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47594065 | TGCATGATTCCATGT[A/G]TATGAAGTATCCAAA | 23607 |
rs770368250 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47479265 | AGTTGGTACTGCTTC[A/G]TATCAACAAACGATC | 23607 |
rs770383303 | in-del | -/TTTTA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47615778 | AATTTTAATTTTAAT[-/TTTTA]TTTAATTTAATTTAA | 23607 |
rs770404893 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47616804 | TGTAACCCCTTGCAT[C/T]TTAGGTTAGGTTTAC | 23607 |
rs770411520 | in-del | -/T | 0.00029878 | 0.0122189 | intron-variant | CD2AP | GRCh38.p7 | 6:47576507 | AAATAGTTTATGCCA[-/T]TTTTTTTCTATTCTA | 23607 |
rs770424942 | snp | A/C | 3.31994e-05 | 0.00407414 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47609149 | CCTTTCAACACCTTC[A/C]AGTGCTTCTAAAGCA | 23607 |
rs770438884 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47522725 | AATTTTTTTCTCTTC[A/G]TTTAGAATACAGGTT | 23607 |
rs770508119 | snp | A/T | 1.96489e-05 | 0.00313433 | intron-variant | CD2AP | GRCh38.p7 | 6:47533582 | TTAACTTGCCTCTTT[A/T]TTTATTTTCCCTTTT | 23607 |
rs770515578 | in-del | -/A | 1.65704e-05 | 0.00287836 | intron-variant | CD2AP | GRCh38.p7 | 6:47581975 | TAAAACTGTCTTCTT[-/A]AAAAAGTATTAATGT | 23607 |
rs770532132 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47485278 | TGACAGCCCTATGCA[C/T]GTTTTTCACCAGTGG | 23607 |
rs770534966 | snp | A/G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47579664 | TAATGTTTCAGTTCC[A/G/T]TACTTTATTCTTCCT | 23607 |
rs770548365 | snp | G/T | 0.000271941 | 0.0116575 | intron-variant | CD2AP | GRCh38.p7 | 6:47599488 | TTAAAAAAAAAAATT[G/T]TCAAAGAAACTCTTT | 23607 |
rs770565875 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47543759 | GCACTATTGCCAGAC[A/G]CATTGGGTGTTAGGG | 23607 |
rs770569798 | snp | A/G | 0.000115786 | 0.00760785 | intron-variant | CD2AP | GRCh38.p7 | 6:47576986 | ATTTGTGTGAGCCAC[A/G]TTATTTACATTCTTT | 23607 |
rs770584350 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47544817 | ACTGTTGTCACTTTT[C/T]AAAAAAAATGGTATA | 23607 |
rs770585307 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47514918 | TTAGCCAGGAGTGGT[A/G]GCACGCACCTGCAAT | 23607 |
rs770594307 | snp | A/T | 1.64942e-05 | 0.00287173 | missense | CD2AP | GRCh38.p7 | 6:47503417 | AATGGGAGAAGAGGA[A/T]TGTTCCCTGACAATT | 23607 |
rs770631239 | in-del | -/AT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47528059 | AATAGTGTGATTCAG[-/AT]ATCATTTCTAATACA | 23607 |
rs770651909 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47506868 | GCGGCTGTGGCAGTT[C/T]CTAAGATGAGACAAC | 23607 |
rs770651976 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47577617 | ATCCTAATGCAAAAT[-/A]AAGAGAAAACCCAGT | 23607 |
rs770672771 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47554022 | AGTCCAGTGCCACAA[C/T]TGGGCTCAGCCTCCC | 23607 |
rs770687599 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47495325 | TCAAGATGGAGGTAG[A/G]GGTTGGAGTTACGTA | 23607 |
rs770690051 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47511595 | ACTGAATTAAGAGTG[C/T]GGGAACTTTCTACTT | 23607 |
rs770707668 | snp | C/T | 1.85699e-05 | 0.00304707 | intron-variant | CD2AP | GRCh38.p7 | 6:47624154 | AAACTAAGGATATTT[C/T]ATGTTTGCTCAATTT | 23607 |
rs770728754 | snp | C/G | 1.67849e-05 | 0.00289692 | missense | CD2AP | GRCh38.p7 | 6:47599372 | AACTAAAGCTAGATT[C/G]TGAACAGCTGCCCCT | 23607 |
rs770735512 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47622420 | TCTCCCTGTGGAGTT[C/T]TACCCCCTGCTTCTC | 23607 |
rs770750324 | in-del | -/CC | 1.66101e-05 | 0.0028818 | intron-variant | CD2AP | GRCh38.p7 | 6:47503267 | GACATTTCGTTTTTT[-/CC]CCCTTTTTTAGTTGA | 23607 |
rs770754810 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47528331 | AGGAGTGTGCCACTA[C/T]GCCTGGCTAATTTTT | 23607 |
rs770762824 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47518718 | GTATTCTGAAGTGAT[G/T]GTCCCATTTCACATT | 23607 |
rs770767773 | snp | A/G | 1.65559e-05 | 0.00287709 | missense, splice-donor-variant | CD2AP | GRCh38.p7 | 6:47576591 | AAACAGATACCGAAG[A/G]TAAAATTAAAGGTAT | 23607 |
rs770774139 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47513075 | AAGAAGAGCTGTAAT[A/G]AAGATTGTAGGATTA | 23607 |
rs770785971 | snp | C/G/T | 3.36243e-05 | 0.00410015 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624234 | TCTTCTTGAGTGGTG[C/G/T]GGACCTGGTGTTCAT | 23607 |
rs770823744 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47600968 | TTTGGGAATTGAAGG[A/C]GTAAAATCTGGAATC | 23607 |
rs770828694 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47531325 | TGTTTATATTTTAAC[A/T]ATTTAACCATTTAAA | 23607 |
rs770840458 | snp | C/T | 1.67214e-05 | 0.00289144 | intron-variant | CD2AP | GRCh38.p7 | 6:47544735 | GTGTTACAGGTAAAA[C/T]AGTAATGGTAATTGA | 23607 |
rs770842137 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47532189 | TAAAGGTTAAGAAAA[G/T]TATACTTGGTTGGCC | 23607 |
rs770869456 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47617493 | GATTTAGCATGTCCC[C/T]AGTTAAATTTATCAT | 23607 |
rs770883676 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47559097 | TTTCTTCTATATTTT[C/G]TAGTTTATTTGCGTA | 23607 |
rs770895414 | snp | C/T | 1.64999e-05 | 0.00287222 | missense | CD2AP | GRCh38.p7 | 6:47580879 | AAACCAAAGAAACCA[C/T]CACCTCCTGCTAAGG | 23607 |
rs770924980 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47552394 | GAGTGAGAACATACG[A/G]TGATTGGTTTTCCAT | 23607 |
rs770925411 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47566921 | ATAGTGCTGTAAATA[C/T]TGTAAACATATGCAT | 23607 |
rs770958766 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47528046 | GTTTGTTTTATTCAA[C/T]AGTGTGATTCAGATA | 23607 |
rs771001887 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47575080 | CTAACTTGCTACGTA[A/T]TTTCTTATGTAGCAG | 23607 |
rs771015496 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47567644 | CCTAGAAGAAGTCAT[A/T]GATTGAGATCCCAAA | 23607 |
rs771022660 | snp | C/G | 1.65869e-05 | 0.00287979 | intron-variant | CD2AP | GRCh38.p7 | 6:47544592 | CTAATTTCTTATTAT[C/G]TTACTTTCTTTAGAG | 23607 |
rs771044785 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47539066 | GGCAATTAATTAAAT[C/T]TGCCACATAAAGCTG | 23607 |
rs771046571 | snp | A/G | | | utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47478103 | CGGGCGGATGGAGGC[A/G]ACTCTTCGCCCCGCC | 23607 |
rs771047336 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47596409 | CTTGACCACATCTTC[C/T]CACTCCCCTCCAACT | 23607 |
rs771076145 | snp | G/T | 1.6734e-05 | 0.00289253 | splice-donor-variant | CD2AP | GRCh38.p7 | 6:47579491 | ATAAAGACTTTCCAG[G/T]AAGCTTTTGTTTTTC | 23607 |
rs771076731 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47612034 | GATTTTAATGTGTTA[C/T]TTAATTTTTAAAAAT | 23607 |
rs771082504 | snp | A/G | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521252 | TAAAAGTTCTTTTCT[A/G]TTAGAAGTGGCATAG | 23607 |
rs771088700 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47548567 | TGGTAATTAAAAAAT[G/T]ACCAACAACAACAAA | 23607 |
rs771130681 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47481849 | AGTGGCATGATCATA[C/G]CTCACTGCAGCCTCA | 23607 |
rs771134883 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47619957 | TTTGTTGTAGATTCT[A/G]GATATTAGTCCTTTG | 23607 |
rs771143770 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47546990 | TGAGAGAATTCACTA[C/T]TACGAAGCCAGTACT | 23607 |
rs771144563 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47526963 | CTGTGAGGTTGATGG[A/G]TGTTATTAATAGCAA | 23607 |
rs771159446 | snp | C/T | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521546 | TGCAGAGTGAGACTC[C/T]GTCTCAAAAAAGAAA | 23607 |
rs771162349 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47539297 | GTGATAATTTAGATG[-/A]AAAGGTAATTTTGTA | 23607 |
rs771171402 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47584017 | GTAATGATATATGAT[G/T]TTGAATATCTTCTCA | 23607 |
rs771172979 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47509309 | CACCATAACAGATAT[A/C]ATGAAGAAGTTTGAA | 23607 |
rs771201197 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47613179 | CTGGGAGTTGGAATC[A/G]TCTTCCAAAATATTG | 23607 |
rs771216980 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47576081 | ATTGTATTTGTTTTA[C/T]TGTAGTTTTTAGAGA | 23607 |
rs771223661 | snp | A/C | 1.65162e-05 | 0.00287365 | missense | CD2AP | GRCh38.p7 | 6:47607955 | CCGAAAAAATCTTGA[A/C]GTTACCAAAAGAAGA | 23607 |
rs771234513 | snp | C/G | 1.65567e-05 | 0.00287716 | intron-variant | CD2AP | GRCh38.p7 | 6:47574260 | AGAAAAGGTGGTAAT[C/G]ATGGACTTGTTAGAT | 23607 |
rs771242715 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47565255 | TCCAAGATAAATTTC[-/T]TTTAGTATTCAGTCT | 23607 |
rs771250445 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47487771 | CTTACTTGATCTGAG[C/G]TCATTGATGCTGGAG | 23607 |
rs771289707 | snp | C/T | 1.64874e-05 | 0.00287113 | missense | CD2AP | GRCh38.p7 | 6:47574168 | ATTCGAGGAATTGGA[C/T]TTGGAGACATTTTTA | 23607 |
rs771290790 | in-del | -/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47505902 | CGGGCGGGGGGCTGA[-/C]CCCCCCCCACCTCCC | 23607 |
rs771345940 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47483142 | CTGCTTAGTTGTAGC[A/G]TTTGATATCTGACTG | 23607 |
rs771384910 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47620868 | TGTTGTTGGTGTATA[A/G]AAGAGCTACTGATTT | 23607 |
rs771412595 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47499615 | CCCTTTCTCCTGGTA[G/T]TTTTCCAGTTTATGA | 23607 |
rs771422617 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47588163 | TTTTCTCATCTTTTA[A/G]ATTCCAGCTTAAAAT | 23607 |
rs771435593 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47493414 | TTGCCTTCATGTTTT[C/G]TGATGAGAAGCCTGC | 23607 |
rs771506855 | snp | C/G | 1.65542e-05 | 0.00287695 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47533697 | ACAACGAATAAGCAC[C/G]TATGGACTTCCAGCT | 23607 |
rs771523764 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47563690 | AGTTAATTTACTCTT[-/A]ACATTAGTTTTTAGC | 23607 |
rs771532329 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47619398 | ACTGCAGATGCTGTT[-/A]AATTCATTCCTTTTT | 23607 |
rs771541056 | snp | A/T | 1.65971e-05 | 0.00288067 | missense | CD2AP | GRCh38.p7 | 6:47595868 | AATCTTAGATGAAAA[A/T]TCAACACTGGAACAG | 23607 |
rs771562831 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47548013 | TCAAAACCTCTGGGA[C/T]AGCAAAGGCAGTGCT | 23607 |
rs771577240 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47534120 | ATAGTGCTTTTTCTT[C/G]AGTTGTTAAACATCT | 23607 |
rs771596486 | snp | A/G | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476261 | CTAGGACTCCTCCAG[A/G]CTGAATTATTGCCTT | 23607 |
rs771598149 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47494887 | AGTTGGCTGGGCATG[A/G]TGGCTCACGCCTGTT | 23607 |
rs771628933 | in-del | -/TAC | | | intron-variant | CD2AP | GRCh38.p7 | 6:47491480 | TAACACTCAATAGTA[-/TAC]TACTGTGATCAGTGA | 23607 |
rs771647164 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47570346 | CTGTTTGTTTTATGA[C/G]TGATAGCAACATACA | 23607 |
rs771661037 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47561884 | CTCCCGGGTTCACGT[A/C]ATTCTCCTGCGTCAA | 23607 |
rs771683983 | snp | A/G | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520718 | GCTACCATGGGCAGG[A/G]CTGGTGCTACAGTTT | 23607 |
rs771686932 | snp | A/T | 1.66665e-05 | 0.00288669 | intron-variant | CD2AP | GRCh38.p7 | 6:47577136 | TTCAGTGAATTGCTT[A/T]ATTTATTTATAGAAA | 23607 |
rs771725813 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47606959 | CCCCCCATCCCTACC[A/G]CCACCACACTAACAC | 23607 |
rs771773577 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47577912 | TTGTTATAAGATGTC[A/G]TAGTGTATATAATTT | 23607 |
rs771797788 | snp | A/G | 1.66676e-05 | 0.00288679 | missense | CD2AP | GRCh38.p7 | 6:47533630 | AGACGGAATTCAAGG[A/G]TGACAGTTTGCCCAT | 23607 |
rs771830000 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47600809 | TATAGCTAGAAATGT[A/G]TTTCATAGGTTATAG | 23607 |
rs771835262 | in-del | -/TTGCTGAAG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47558190 | TTGTATCCTGAGACT[-/TTGCTGAAG]TTGCTTATCAGCTTA | 23607 |
rs771863187 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47547423 | TCAACAGCAGTTTAA[A/T]AAGACAAAGAGGGAC | 23607 |
rs771871958 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47601143 | TAGTAAAAATAATAT[A/G]TGTAATAATTTCAAA | 23607 |
rs771887040 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47529560 | AGGTGCATAAATAGT[C/T]ATCTTACTGGTTTTT | 23607 |
rs771937457 | snp | A/C | 1.69072e-05 | 0.00290746 | missense | CD2AP | GRCh38.p7 | 6:47599419 | GACTTTGATTCACTT[A/C]CAGTAAGGACCTCCA | 23607 |
rs771943357 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47518360 | TATCTGCAAAAGTTA[A/G]TGTTCTACTGCATTT | 23607 |
rs771969506 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47509490 | TGAAGCGAAGTGCAG[C/T]AAAACGAGGTAGGCC | 23607 |
rs772031805 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47614897 | TAAACTTAAGAGTTT[A/G]TCTTAATTCTCCACT | 23607 |
rs772034760 | snp | C/T | 3.30246e-05 | 0.0040634 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47544694 | GGGAGATATTATTGA[C/T]ATTAATGAAGAGGTA | 23607 |
rs772049210 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47530572 | TTGTTTATTCATTTA[C/T]TTGATGGATGTTTGG | 23607 |
rs772060279 | snp | C/T | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47477457 | CAGAAAGTAACTCCG[C/T]GTCGCCGCCGCGGAA | 23607 |
rs772078303 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47579229 | GGTCCCAGCCACTTG[A/G]GAGGCTGAGTTGGGA | 23607 |
rs772081970 | in-del | -/CTCCTTCCCT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497307 | GTTCCCGTTCCCTTT[-/CTCCTTCCCT]TTCCTTTCCTTTCCT | 23607 |
rs772095099 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47525819 | TTCTTATCTATATGG[A/T]GATTATCCATATTGT | 23607 |
rs772109612 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47523407 | TTGTATACCTTAAGT[A/G]TATGCAATTTTTATT | 23607 |
rs772139570 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47516875 | ATAGCATATGATTTT[A/G]TATTTAGTGCAGCAC | 23607 |
rs772159529 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47588099 | TTTTTTAGGGGACAT[A/C]CTTCTTTCTCTGGAA | 23607 |
rs772183451 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47552241 | GAGATTTTGGTGCAC[A/C]CATCACCTGAGCAGT | 23607 |
rs772216145 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47481211 | AATATTTGTGAATTT[G/T]TATTTTTGGAAGAGT | 23607 |
rs772216829 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47615319 | AAAAAGTAGGGTTTG[G/T]AATGATAGTATTAGG | 23607 |
rs772227398 | snp | A/T | 1.65023e-05 | 0.00287244 | missense | CD2AP | GRCh38.p7 | 6:47554696 | CAAGTTGGGACTGTT[A/T]CCCTCAAATTTTGTG | 23607 |
rs772238434 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47486348 | GAATGTCATGAATGT[A/G]TTGGGATGGCTTATG | 23607 |
rs772249505 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47574877 | GTGGTAAAATAGCTA[C/T]AGTCTGTAGAACATT | 23607 |
rs772263462 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47551145 | TAAAGAACTTACTTA[A/T]GTAACCTAACACCAC | 23607 |
rs772264955 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497925 | GACTGTTTGTTCCTT[A/G]GATTTGTTGCGCAGC | 23607 |
rs772280634 | snp | C/T | 3.37747e-05 | 0.00410928 | intron-variant | CD2AP | GRCh38.p7 | 6:47544747 | AAACAGTAATGGTAA[C/T]TGATGCTATGGATTT | 23607 |
rs772289650 | snp | C/G | 1.70171e-05 | 0.00291689 | intron-variant | CD2AP | GRCh38.p7 | 6:47608068 | TTGTTGACTTTCTGG[C/G]ATTCTTTGTGGACAT | 23607 |
rs772298762 | in-del | -/AA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47586924 | AAGAGAAGGCATAAC[-/AA]AGGAAATGATTCTAA | 23607 |
rs772360705 | snp | A/G | 1.64792e-05 | 0.00287042 | missense | CD2AP | GRCh38.p7 | 6:47503382 | AGCTACAGGAGGAAG[A/G]GTGGCTGGAAGGAGA | 23607 |
rs772365482 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47532930 | AATTTTATACTTTTC[C/T]ATGATGGTTCACATG | 23607 |
rs772380215 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47540056 | AGTATGGTGGTGAGC[A/G]CCTGTGGTCCCAGCT | 23607 |
rs772388478 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47502876 | TTACGCCCTGCCATC[A/T]TATTCTGTTGGTTAG | 23607 |
rs772396255 | snp | C/G | 1.70321e-05 | 0.00291818 | missense | CD2AP | GRCh38.p7 | 6:47609127 | TACGTTTTCAGCCAT[C/G]TGTGTACCTTTCAAC | 23607 |
rs772401230 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47596207 | TGTTTTAAAGCGTAT[A/G]TATAATTCATTGTGG | 23607 |
rs772446333 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47592724 | AGAGTTTAGAGAGCT[C/T]ATGGGTTTGTGAACA | 23607 |
rs772451959 | snp | C/G | 0.000133721 | 0.00817574 | intron-variant | CD2AP | GRCh38.p7 | 6:47503245 | GTATTTTGTGAATTA[C/G]ATTTTAGACATTTCG | 23607 |
rs772453931 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47509611 | AGCAAGGTCACTTCA[-/T]TTTTTTGTTTTATGA | 23607 |
rs772477442 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47504445 | GTATCCAGGAAACAC[C/T]GTGGATACCAAAATA | 23607 |
rs772479408 | snp | C/G | 3.30082e-05 | 0.00406239 | missense | CD2AP | GRCh38.p7 | 6:47580894 | CCACCTCCTGCTAAG[C/G]CTCCAGGTATGTAAG | 23607 |
rs772490697 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47582409 | CCCAGTTCCTACTTA[A/G]GCATGAAAATAATTA | 23607 |
rs772518474 | in-del | -/CAA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47557560 | GCTAGCCAGTTTTTC[-/CAA]CAACATTTATTAAAT | 23607 |
rs772525144 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47594685 | GTATAATTATATATA[A/G]TACATTGTTACATCT | 23607 |
rs772541761 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47526729 | ACTTTCAAGAGGAAC[A/C]GGATTTGAATAGTAA | 23607 |
rs772554140 | in-del | -/GGAG | 9.07153e-05 | 0.0067342 | utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47478194 | CGAGCCACCACTGGA[-/GGAG]GGAGGAGGAGGAGGA | 23607 |
rs772558028 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47566277 | TTGCTTATTAAGCTT[A/T]TTGTCTGTCTACCTG | 23607 |
rs772572598 | snp | A/G | 1.6492e-05 | 0.00287154 | missense | CD2AP | GRCh38.p7 | 6:47503414 | CTAAATGGGAGAAGA[A/G]GAATGTTCCCTGACA | 23607 |
rs772589770 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47480757 | AATCTCAATTTTTGA[C/T]CTTTGTTAGAAGTAG | 23607 |
rs772670792 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47509972 | TATTTCTACTATTAG[C/G]AATGATTTATCATGG | 23607 |
rs772699707 | in-del | -/T | 6.76407e-05 | 0.00581513 | intron-variant | CD2AP | GRCh38.p7 | 6:47579501 | TCCAGTAAGCTTTTG[-/T]TTTTCAATGATGATA | 23607 |
rs772700438 | snp | A/G | 1.65723e-05 | 0.00287852 | intron-variant | CD2AP | GRCh38.p7 | 6:47574272 | AATGATGGACTTGTT[A/G]GATTAACTCCACTCA | 23607 |
rs772700606 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497161 | TGTTTTTTTTTTACT[C/G]TGAAGCCAAGTAGTA | 23607 |
rs772798526 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47564089 | ATTTATTTGAGAGTA[C/T]TCGATAACAATTCTG | 23607 |
rs772801670 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47537368 | TTCTGACTGGTAAGG[A/G]GAAAAAGACTCACTC | 23607 |
rs772831578 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47494987 | CAGTATAATGAGACC[A/T]TGTCTCTACAAAAAA | 23607 |
rs772843395 | snp | G/T | 1.66181e-05 | 0.00288249 | intron-variant | CD2AP | GRCh38.p7 | 6:47503262 | TTTTAGACATTTCGT[G/T]TTTTCCCCCTTTTTT | 23607 |
rs772845425 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47529562 | GTGCATAAATAGTTA[C/T]CTTACTGGTTTTTAT | 23607 |
rs772846141 | in-del | -/TTTTTTT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47553515 | CCACACCTAGTGAAT[-/TTTTTTT]TTTTTTTTTTTTTTT | 23607 |
rs772868791 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47493614 | TGTACCTTATTATTT[C/T]TGGAAAATTCTTAGC | 23607 |
rs772873365 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47550953 | AACCAAACATCATAT[A/G]TTCTCACTTGTAAGT | 23607 |
rs772917724 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47617949 | CTCATCTTCTAATGC[A/C]CACGTTCTACAGATT | 23607 |
rs772957948 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47603375 | TTCTATCATGGGCTA[A/G]AGACTAAAACTTGAC | 23607 |
rs772962778 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47530605 | TGTTTTGAGTTTTTG[A/G]ATATTTATTACACTG | 23607 |
rs772979402 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47510603 | ATTTGATTTTTATGT[A/C]AAATACAGCATAAGT | 23607 |
rs772992331 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47536884 | TGTTTCAGCATCAGA[A/C]TATTAGCAGTCAGCG | 23607 |
rs773006934 | snp | G/T | 3.53188e-05 | 0.00420216 | intron-variant | CD2AP | GRCh38.p7 | 6:47599276 | TTCATACTAGTGATT[G/T]TTGCGTGTTTTTTTC | 23607 |
rs773039196 | in-del | -/GTAT | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624721 | TGTGTGTGTGTGTGT[-/GTAT]ATATATATATATATT | 23607 |
rs773044847 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47619370 | GAATAATAGTCTCCA[A/G]TTTCATGCAGGTCAC | 23607 |
rs773053686 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47577406 | ACTTCCCAGGTTTTT[-/A]ATTCTTACTTCTCTT | 23607 |
rs773066834 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47565453 | TTTTATGAAACCAGT[A/G]ACTGTATATACTTGT | 23607 |
rs773067251 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47552288 | GTGTAGTCTTTTATC[A/C]CTTGCCACCCCCATT | 23607 |
rs773067830 | in-del | -/AA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47511074 | GAGACTCTGTGTCTC[-/AA]AAAAAAAAAAAAAAA | 23607 |
rs773086195 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47615052 | TTAGAGACTCTTCCC[A/G]TTGTTTAAGTATTTC | 23607 |
rs773094755 | snp | C/G | 1.66632e-05 | 0.0028864 | intron-variant | CD2AP | GRCh38.p7 | 6:47544584 | TTCTTAATCTAATTT[C/G]TTATTATGTTACTTT | 23607 |
rs773114636 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47509176 | GGTAGGAAATGACCA[A/G]TTGGTGGAACAGTTA | 23607 |
rs773116742 | snp | C/G | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47477508 | CAGCAGAAACCTTTT[C/G]ATCCATCTGAGGCGA | 23607 |
rs773124622 | in-del | -/TT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47508535 | AACTTTCTTTCTTTC[-/TT]TTTTTTTTTGTTTTT | 23607 |
rs773139261 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47616658 | CCCATTTAGGTCTAG[C/T]TGCCTTCTTGATGTA | 23607 |
rs773153532 | snp | A/C | 1.67452e-05 | 0.0028935 | missense | CD2AP | GRCh38.p7 | 6:47533743 | CATCCACAAACCAAA[A/C]ACATTAAGAAGAGTA | 23607 |
rs773175274 | snp | A/T | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476005 | CTTTAAATATTAAGG[A/T]TTCTAGAGACCTAGA | 23607 |
rs773177781 | snp | C/G | 0.000318035 | 0.0126062 | intron-variant | CD2AP | GRCh38.p7 | 6:47612442 | ATTATTTAATCGAAA[C/G]ACTTAACAGTAATAA | 23607 |
rs773187230 | snp | A/C/T | 6.65325e-05 | 0.00576731 | intron-variant | CD2AP | GRCh38.p7 | 6:47503259 | AGATTTTAGACATTT[A/C/T]GTTTTTTCCCCCTTT | 23607 |
rs773216411 | snp | A/C | 1.6582e-05 | 0.00287936 | missense | CD2AP | GRCh38.p7 | 6:47579479 | TAAATGAACTTGATA[A/C]AGACTTTCCAGTAAG | 23607 |
rs773221743 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47516988 | TGAAATGTGATTCCT[A/G]ATATGGGAGGTGGGG | 23607 |
rs773222320 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47513401 | TTCTAGTTATTATTT[A/G]TTTTCGTTTATAGTG | 23607 |
rs773234554 | snp | A/G | 1.8052e-05 | 0.00300428 | intron-variant | CD2AP | GRCh38.p7 | 6:47579357 | AAAAAAAGGTCTATT[A/G]TCTTAATTATTCTAT | 23607 |
rs773241556 | in-del | -/GAA | 0.00103135 | 0.0226851 | cds-indel | CD2AP | GRCh38.p7 | 6:47599310 | TTCAGGATTAATGGG[-/GAA]GAAGTTTCTAGCATT | 23607 |
rs773241638 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47525838 | TATCCATATTGTATT[C/T]TTTCTTGGCAAGTTT | 23607 |
rs773262751 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47552869 | GCTTGTATTCTAGCA[C/T]CCATTTTTATTTTAG | 23607 |
rs773265101 | in-del | -/CT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47489402 | GCTGGTTTCGAACTC[-/CT]GACCTCAGGTGATCT | 23607 |
rs773265672 | snp | G/T | 5.15823e-05 | 0.00507824 | utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47478196 | GAGCCACCACTGGAG[G/T]AGGAGGAGGAGGAGC | 23607 |
rs773314952 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47487419 | TTCTTGGCCAGGCGC[A/G]GTGGCTCACGCCTGT | 23607 |
rs773353818 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47588141 | TCAGAATCTTTCATG[A/G]CCAGGTTTTTCTCAT | 23607 |
rs773371148 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47537898 | GGAATTACAGGAACA[A/C]GCCACTGCACCTGGC | 23607 |
rs773391885 | snp | A/G | | | synonymous-codon | CD2AP | GRCh38.p7 | 6:47544706 | TGATATTAATGAAGA[A/G]GTAAGGAAAAAATGT | 23607 |
rs773413172 | snp | C/T | 1.65384e-05 | 0.00287557 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47607941 | GCCAACTCACAGCCC[C/T]GAAAAAATCTTGAAG | 23607 |
rs773475335 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47502949 | ACATAAGGACATGAA[C/T]ACGAGGAAGTGGGGA | 23607 |
rs773479372 | in-del | -/A | 1.64985e-05 | 0.0028721 | frameshift-variant | CD2AP | GRCh38.p7 | 6:47609224 | GAAACAGATGATGTG[-/A]AAAAAAAATTCCCTG | 23607 |
rs773487090 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47597734 | CCTGTGGCTTTTGCA[A/G]AAGTATGGTGGAATT | 23607 |
rs773497919 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47582627 | AGAAACTTGAATACT[A/G]TTTTAGAATGCTTTT | 23607 |
rs773513133 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47533905 | AGTTATTGCCCTGTG[C/T]AGTCAATCTTAATTT | 23607 |
rs773514692 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47572331 | TCTTGTTGTATTTAC[A/G]TGGTGCGACATTTGT | 23607 |
rs773518439 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47541514 | AAGGGGAAAAAACCT[C/T]ACACAGATGTAACTT | 23607 |
rs773530119 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47572938 | TTTAACAGACTACCT[C/T]AGTTCAGTGAACTGT | 23607 |
rs773558187 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47594769 | ACTAAGCTATATTTT[C/G]ATATGATTCAAAGTA | 23607 |
rs773600809 | snp | C/T | 1.64882e-05 | 0.00287121 | missense | CD2AP | GRCh38.p7 | 6:47609262 | TTAGAGCCCAGATTA[C/T]TGAATTGTTGTGCAT | 23607 |
rs773639381 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47623260 | TTTAATAATGTGCTG[C/T]TTGTCGAAGCTAGCC | 23607 |
rs773650599 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47493248 | CCTTTAACATGTCTT[C/T]TGTGTTGGGTCTGTT | 23607 |
rs773684137 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47617884 | TGCCTCTTACAATTG[A/G]TAAGTCCGAATTTTT | 23607 |
rs773691167 | snp | A/G | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520382 | ATGAATTGTGCCAAA[A/G]TCCAGTGCCTCACTT | 23607 |
rs773705722 | snp | A/G | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521198 | TTGCTTATCTTGCTC[A/G]TAAGTAAGGTTTTTA | 23607 |
rs773716494 | snp | C/G | 1.65861e-05 | 0.00287972 | intron-variant | CD2AP | GRCh38.p7 | 6:47582072 | AAGAAAAGGGTGAGG[C/G]TAATTTTCAACTTTC | 23607 |
rs773723623 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47539697 | TAATGCTTTGTTGTG[C/T]GGGAGATGTGAAGAA | 23607 |
rs773730382 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47611954 | ATTAGAAGGGAACAC[A/G]GGAAGGTGAAAAGAT | 23607 |
rs773789313 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497973 | TTTTATTCTGAGGTT[A/G]GTGCCACTATTTCTT | 23607 |
rs773850919 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47590216 | CTTTAAAGTAACTGT[A/G]CTTAATAAATGTTAG | 23607 |
rs773888673 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47479746 | TGACCTGGGGATGCA[C/G]TCTTGTTTTGCATAT | 23607 |
rs773889150 | snp | A/G | 9.93394e-05 | 0.00704697 | missense, intron-variant | CD2AP | GRCh38.p7 | 6:47576593 | ACAGATACCGAAGGT[A/G]AAATTAAAGGTATGT | 23607 |
rs773896291 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47509762 | TTAGACAAATCACAT[A/G]ATTTCCCTGTTTTCT | 23607 |
rs773898361 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47491482 | AACACTCAATAGTAT[A/G]CTGTGATCAGTGATA | 23607 |
rs773908718 | snp | G/T | 1.65853e-05 | 0.00287964 | missense | CD2AP | GRCh38.p7 | 6:47609151 | TTTCAACACCTTCCA[G/T]TGCTTCTAAAGCAAA | 23607 |
rs773972224 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47557020 | ATGATCGCCATTCTA[A/T]CTGGCATGAGATGGT | 23607 |
rs773986777 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47606778 | TATCAGGGTAAATGC[A/G]GTATCCATCACGTCA | 23607 |
rs774015514 | snp | A/C | 1.65381e-05 | 0.00287555 | intron-variant | CD2AP | GRCh38.p7 | 6:47576989 | TGTGTGAGCCACATT[A/C]TTTACATTCTTTATT | 23607 |
rs774027296 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47591249 | GTGGAAGCAGGTGGG[G/T]TAGTGATTGGGAAGA | 23607 |
rs774028312 | in-del | -/G | 0.000216185 | 0.0103945 | intron-variant | CD2AP | GRCh38.p7 | 6:47599254 | ACAATTTAAAAAAAA[-/G]TCGTGTTTCATACTA | 23607 |
rs774030509 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47568986 | AGGGAGGCAGGGCAA[A/T]AGTGTCAGATATTAC | 23607 |
rs774039149 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47514919 | TAGCCAGGAGTGGTG[A/G]CACGCACCTGCAATC | 23607 |
rs774063659 | snp | G/T | 3.51327e-05 | 0.00419108 | intron-variant | CD2AP | GRCh38.p7 | 6:47533598 | TTTATTTTCCCTTTT[G/T]TAGGAAATTAAAAGA | 23607 |
rs774081495 | snp | C/G | 0.000151328 | 0.00869719 | missense | CD2AP | GRCh38.p7 | 6:47599401 | CTTAGACCAAAATCA[C/G]TAGACTTTGATTCAC | 23607 |
rs774091424 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47531486 | ACAGGAGGATTGTTT[A/G]TTTAAGGTATGTACT | 23607 |
rs774100710 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47553399 | TTGCCCAGGATGGAG[A/G]GCAGTGGCGCCATCT | 23607 |
rs774152199 | in-del | -/T | 0.0186581 | 0.0947676 | intron-variant | CD2AP | GRCh38.p7 | 6:47609103 | AAATAAAATCAGAAA[-/T]TTTTTTTTTACGTTT | 23607 |
rs774186224 | in-del | -/TAA | | | utr-variant-3-prime, cds-indel | CD2AP | GRCh38.p7 | 6:47626420 | TCACAAAATGATATT[-/TAA]TAATAACCTTGGGGT | 23607 |
rs774203901 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47577664 | CAGAATCCTATAATA[A/T]CTAGTATTATGGGAA | 23607 |
rs774207236 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47565293 | AGCATTGCTTTGCTA[A/G]GAAAGTGTTATGTTT | 23607 |
rs774222398 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47627159 | TCAGTCTTTATTGGT[A/T]ATTTTTTGTTAACTT | 23607 |
rs774258657 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47515740 | CAGCATAGTTGAAAG[A/C]TCTTAGCATTATAAA | 23607 |
rs774275105 | in-del | -/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47483811 | TTTTTTTTTTTTTTT[-/G]CTCCTGTCTCTTTTT | 23607 |
rs774293179 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47504480 | ATGCTCAGATCTGTT[-/A]ATATAAAATGGCATA | 23607 |
rs774306719 | snp | G/T | 1.82597e-05 | 0.00302151 | intron-variant | CD2AP | GRCh38.p7 | 6:47624160 | AGGATATTTTATGTT[G/T]GCTCAATTTATGTTT | 23607 |
rs774316513 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47558504 | TATGTTCCATCAATA[C/T]CTAGTTTGTTGAGTT | 23607 |
rs774323414 | snp | C/T | 0.000173316 | 0.00930742 | intron-variant | CD2AP | GRCh38.p7 | 6:47599291 | TTTGCGTGTTTTTTT[C/T]TTATTTCAGGATTAA | 23607 |
rs774334765 | snp | G/T | 1.65512e-05 | 0.00287669 | intron-variant | CD2AP | GRCh38.p7 | 6:47544598 | TCTTATTATGTTACT[G/T]TCTTTAGAGACCAAG | 23607 |
rs774340839 | in-del | -/TTTTTTTT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47489166 | CTGCACTCAACTAGT[-/TTTTTTTT]TTTTTTTTTTTTTTG | 23607 |
rs774345050 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47485951 | CTCTATGATGTTCAC[A/G]CATGGACCAAATTGC | 23607 |
rs774396379 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47536396 | CATAAGGTTAATAGT[C/G]TAAACACTGCAGTGT | 23607 |
rs774442728 | in-del | -/AT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47539273 | AACTGTATGAGAGAC[-/AT]ATGTGTAGTGATAAT | 23607 |
rs774474931 | snp | A/G | 1.67393e-05 | 0.00289299 | intron-variant | CD2AP | GRCh38.p7 | 6:47544737 | GTTACAGGTAAAACA[A/G]TAATGGTAATTGATG | 23607 |
rs774503674 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47587038 | AGTGACCTTTGGACA[C/T]ATGCATTCAGAGAGG | 23607 |
rs774529187 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47609995 | GAGTTGGACATTTAT[A/G]AAATGAATGTGTTGG | 23607 |
rs774566131 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47501275 | TGCTTATTTGAAAAC[C/T]ATTCACTGTGTATGT | 23607 |
rs774591639 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47572531 | TAGCATTATATTTCT[G/T]AAGTTAATAACTTGT | 23607 |
rs774596171 | snp | C/T | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476219 | TCAGAAATACTCTGT[C/T]TGCATATCCACTTCC | 23607 |
rs774607411 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47581225 | TTTCAAATGAAATCC[A/G]TTTGTTAATGTCTCA | 23607 |
rs774612078 | snp | A/C | 1.65012e-05 | 0.00287234 | missense | CD2AP | GRCh38.p7 | 6:47580886 | AGAAACCACCACCTC[A/C]TGCTAAGGCTCCAGG | 23607 |
rs774666291 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47483645 | CTACATTAGTAGTCT[A/G]CATTAGTAGCTGAAT | 23607 |
rs774669667 | snp | A/G | 1.67891e-05 | 0.00289729 | intron-variant | CD2AP | GRCh38.p7 | 6:47503229 | ATTAATATAGTTTAC[A/G]GTATTTTGTGAATTA | 23607 |
rs774669883 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47565323 | TCGGTTTTGTAATGT[C/G]TCCTTTTTAATTTTG | 23607 |
rs774676097 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47547944 | GGGTCAGAAATGAAA[-/T]CAAGATGGAAATTAA | 23607 |
rs774722436 | snp | A/C | 1.65081e-05 | 0.00287293 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47607962 | AATCTTGAAGTTACC[A/C]AAAGAAGAAGACAGT | 23607 |
rs774732241 | snp | C/T | 1.64837e-05 | 0.00287081 | missense | CD2AP | GRCh38.p7 | 6:47595977 | TCTTCTGGAACAGTG[C/T]ACCCAAAGCGACCTG | 23607 |
rs774767075 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47493515 | GCCTTTGATTTTCTT[C/T]CATTAAATGTGATAC | 23607 |
rs774767620 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47585922 | TCTATCTTGGAAATA[C/T]GGCCAACAAATTCCA | 23607 |
rs774792083 | snp | A/C | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625245 | TTCAGTGTGAGGTTT[A/C]CTATTTTGACAAGTT | 23607 |
rs774796426 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47608542 | GTTTCCTCCCAAATT[A/G]TTTCTTGATTTCATT | 23607 |
rs774798567 | snp | C/T | 1.64914e-05 | 0.00287149 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47574179 | TGGATTTGGAGACAT[C/T]TTTAAAGAAGGCTCT | 23607 |
rs774852008 | snp | C/T | 1.64762e-05 | 0.00287016 | missense | CD2AP | GRCh38.p7 | 6:47574091 | CTGGGCCTACTTCAC[C/T]TATACCTTCTCTGGG | 23607 |
rs774860601 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47525721 | TTTAACTTCCCCCAC[C/T]ATTTGCATATGTATT | 23607 |
rs774874934 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47623030 | CTTTAATAACAGATC[A/G]GGCTGACAATGAAAG | 23607 |
rs774898073 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47604727 | ATATATTTAAATTCA[A/G]CCGCCTTCAGATTAT | 23607 |
rs774904163 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47620818 | TGCAGATACTGTAAA[A/T]GGGGTTGAGTTCTTG | 23607 |
rs774904411 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47496626 | ATCTTGTCAAAGTAA[C/T]TCCTGCACGTGATAT | 23607 |
rs774916936 | snp | A/G | 0.000120997 | 0.00777715 | intron-variant | CD2AP | GRCh38.p7 | 6:47606326 | ATTTAGCAAATGCAG[A/G]GTCCATTGGAAGATA | 23607 |
rs774926642 | snp | C/T | 1.66048e-05 | 0.00288134 | intron-variant | CD2AP | GRCh38.p7 | 6:47609338 | CTCCTGTGAGTACTA[C/T]TTAACCCATGCATAA | 23607 |
rs774952340 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47513333 | AATAGCTACTGAAGA[A/G]TTCTTCAGTCATGAC | 23607 |
rs774956823 | in-del | -/ATGAC | | | intron-variant | CD2AP | GRCh38.p7 | 6:47602235 | GATTTTCTTTTTTTA[-/ATGAC]ATGACATAACTTTTT | 23607 |
rs774962467 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47560244 | TATCTTTATTCTTTA[C/G]TATTTCAATGTGTAT | 23607 |
rs774996552 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47590764 | GGAGGGAGAAAAAAA[C/T]GGAGCAGAAACTGTA | 23607 |
rs775037020 | in-del | -/CCTGTCCGCCATGATGATC | | | intron-variant | CD2AP | GRCh38.p7 | 6:47622848 | AATCTAGTCTTGCCT[-/CCTGTCCGCCATGATGATC]CCTGTCCAGTGATAA | 23607 |
rs775040657 | snp | A/G | 1.6537e-05 | 0.00287545 | missense | CD2AP | GRCh38.p7 | 6:47609168 | GCTTCTAAAGCAAAT[A/G]CAACTGCTTTCCTGA | 23607 |
rs775045314 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47523080 | TTTAGTTTTAAAAAT[C/G]TTTTGCTTTATGAAA | 23607 |
rs775052955 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47567174 | TCCATTTGTTTGCTG[C/G]TATCTTCATCTAATT | 23607 |
rs775054666 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47622436 | TACCCCCTGCTTCTC[G/T]GGCTGCCCTCCCTAT | 23607 |
rs775119406 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47600593 | TATTTACTACTAATT[-/T]CTGGGAATTGAAATG | 23607 |
rs775126668 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47527051 | TTTCATGTTTTGTAC[C/T]TAGTAATTTTTCAAA | 23607 |
rs775151838 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47554408 | ATTGCGATTGATTAC[A/G]AATTGTCATTGTAAA | 23607 |
rs775171218 | snp | C/G | 1.65573e-05 | 0.00287721 | missense | CD2AP | GRCh38.p7 | 6:47533711 | CCTATGGACTTCCAG[C/G]TGGAGGAATTCAGCC | 23607 |
rs775183449 | snp | A/G | 0.000181364 | 0.00952098 | missense | CD2AP | GRCh38.p7 | 6:47609276 | ATTGAATTGTTGTGC[A/G]TTGTAGAAGCACTGA | 23607 |
rs775209266 | in-del | -/TGTC/TT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47499313 | GTATGTGCATGTGTG[-/TGTC/TT]TGTGTGTGTGTGTTG | 23607 |
rs775227205 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47559662 | CATTAAGATTATTAC[C/T]AAAGTTAATGTGCTC | 23607 |
rs775231339 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47616995 | TTTTTAGAGACAGGG[A/T]GTCACTCTGTCACCC | 23607 |
rs775236012 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47578344 | TAGCTGAGACTACTA[C/T]AGTTGCATCCCATTG | 23607 |
rs775253003 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47582352 | GCTTTTATTATTTTT[A/T]TAGTGTTTCAGTTTT | 23607 |
rs775263467 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47576330 | ACAAGGAATCTTTAA[A/G]TTGGTAGCTCTGAGC | 23607 |
rs775279393 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47562751 | GCCAAGCCTTAGACA[A/G]GTGGCAAGCTCATGT | 23607 |
rs775282919 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47617827 | GAGGTGTTTTTATAA[A/T]TTGGTCCTAGCTATC | 23607 |
rs775306683 | in-del | -/ATTT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47531371 | ACTGAAAGAAAAAAC[-/ATTT]ATTCTTAATCAGAAT | 23607 |
rs775320573 | in-del | -/TG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47582793 | TGTTTTTTTTTGTTT[-/TG]TGTTTTTTTTTTTTT | 23607 |
rs775329134 | snp | A/G | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626932 | TTAAAAGTTGCTGCT[A/G]TGAATATTTTTGGCT | 23607 |
rs775340984 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47508310 | TTGCAGCTTCTCTGT[C/T]AGCACTAGCTGCTTC | 23607 |
rs775342019 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47589856 | TTCCTAAAGGGATTT[A/G]CTGTTGGAGGAAGTA | 23607 |
rs775355439 | in-del | ACAGGATCTC/GAACTCTAGTTCCATCCATGT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47607128 | TCCATGTTGCAAATG[lengthTooLong]ATTCTTTTTTGTGAC | 23607 |
rs775356238 | snp | G/T | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625158 | CATTATCTTGTCACT[G/T]AGTTCTTCATGTTTC | 23607 |
rs775408503 | snp | A/G | 1.6908e-05 | 0.00290753 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47599421 | CTTTGATTCACTTAC[A/G]GTAAGGACCTCCAAA | 23607 |
rs775425376 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47528275 | CGCCTCCTGGGTTCA[A/T]GTGATTCTCATACCT | 23607 |
rs775449594 | snp | G/T | 0.000215476 | 0.0103775 | intron-variant | CD2AP | GRCh38.p7 | 6:47576606 | GTAAAATTAAAGGTA[G/T]GTTTTTGAATAAAGC | 23607 |
rs775456090 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47569486 | AGGAGATGAAGAGGT[C/T]CCAGCAGGGATTCTT | 23607 |
rs775492407 | snp | A/G | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476391 | TCATACTGTTAATTA[A/G]CTTTGTGTTCGTATC | 23607 |
rs775530325 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47539592 | ATGGATATAATTTTA[A/G]TTTTGCCTCATTTTA | 23607 |
rs775596297 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47501045 | AGCCACTGAGCCTGG[C/T]CTGTGTTTTGTTTTT | 23607 |
rs775602375 | snp | A/G | 1.68658e-05 | 0.0029039 | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624248 | GTGGACCTGGTGTTC[A/G]TAATGTTCCAGGGAT | 23607 |
rs775628489 | in-del | -/TGATTTTTC/TGATTTTTCATCTAAG/TGATTTTTCATCTAAGATTTAA | 8.2414e-05 | 0.00641885 | cds-indel, frameshift-variant | CD2AP | GRCh38.p7 | 6:47595977 | CTTCTGGAACAGTGT[lengthTooLong]ACCCAAAGCGACCTG | 23607 |
rs775704123 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47599511 | AACTCTTTAAGAGAT[A/G]TATTTATGCAATTTG | 23607 |
rs775709162 | in-del | GGGAGTAGGTA/TTTTTTTTTTTT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47616084 | CCACTGCGCCTGGCC[GGGAGTAGGTA/TTTTTTTTTTTT]TTTTTTTTTTTTTTT | 23607 |
rs775723720 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47515538 | GTCTTGCTGGTAATA[C/T]GGGCTAAAAACTTGA | 23607 |
rs775727317 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47563753 | AAAGTAATGAAAAAA[C/G]CGTGAGCTCCCTGGC | 23607 |
rs775730089 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47559803 | AATTCTTGTATGGAG[C/T]CTGCAGAAGAGTCAG | 23607 |
rs775738066 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47613334 | ATAGCCTTCCAAAAT[C/G]TGTATCTTAAATAAT | 23607 |
rs775738806 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47585682 | AGTACTCAGATCTGT[A/C]GACAGCTTACTGTGA | 23607 |
rs775759148 | snp | C/G | 1.65026e-05 | 0.00287246 | missense | CD2AP | GRCh38.p7 | 6:47554697 | AAGTTGGGACTGTTT[C/G]CCTCAAATTTTGTGA | 23607 |
rs775812493 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47554595 | TCCCATAGGGTGACG[A/G]TTTTCACTTAACAGA | 23607 |
rs775816689 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47615605 | TTACTCATCATGAAG[C/G]GGATGATCCAAACAT | 23607 |
rs775817246 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47608131 | CGAATTATTTTTTCT[A/G]CCAAGAAATGAAATA | 23607 |
rs775821650 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47548479 | GAATTCCTGTAAAGA[C/T]ACAATCCTCCTTGAT | 23607 |
rs775834580 | snp | A/G | 1.65037e-05 | 0.00287256 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47607992 | TGCCAACCTGAAGCC[A/G]TCTGAATTAAAAAAA | 23607 |
rs775865477 | snp | A/G | 1.65094e-05 | 0.00287305 | intron-variant | CD2AP | GRCh38.p7 | 6:47580903 | GCTAAGGCTCCAGGT[A/G]TGTAAGAAGCATATT | 23607 |
rs775866111 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47540485 | TTTTTCTTTTTAAAA[G/T]AAATGACTCATAATT | 23607 |
rs775867953 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47613562 | CTTAAAATATTCAGT[A/G]AATCATGCTGTAAAC | 23607 |
rs775910345 | snp | A/T | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47625943 | TAGAATAGGTTTAAA[A/T]GACTAGTCAAATGAA | 23607 |
rs775911444 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47603676 | TATTCATTCTACAGC[C/T]GTTCTTTTTTCCTGT | 23607 |
rs775911715 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47558329 | TTCTTTCTCTTGCCT[C/G]ATTGCCCTGGCCAGA | 23607 |
rs775922130 | in-del | -/TAGTTCCATCCATGT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47607137 | AAATGACAGGATCTC[-/TAGTTCCATCCATGT]ATTCTTTTTTGTGAC | 23607 |
rs775978776 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47607118 | TCTAGTTCCATCCAT[A/G]TTGCAAATGACAGGA | 23607 |
rs775985372 | snp | A/G/T | 0.000393701 | 0.014025 | intron-variant | CD2AP | GRCh38.p7 | 6:47608076 | TTTCTGGGATTCTTT[A/G/T]TGGACATCAAACATA | 23607 |
rs775987563 | snp | A/G | 1.65858e-05 | 0.00287969 | intron-variant | CD2AP | GRCh38.p7 | 6:47574278 | GGACTTGTTAGATTA[A/G]CTCCACTCATTCTCT | 23607 |
rs776007901 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47569575 | ACAAAACATTTAAGA[A/C]ACCCTGATGGATTGT | 23607 |
rs776063896 | snp | A/C | 0.000157946 | 0.00888527 | intron-variant | CD2AP | GRCh38.p7 | 6:47579530 | TAATACTTGAAAGAA[A/C]ATTTTGCCACTATTC | 23607 |
rs776092446 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47522811 | TATTTGCAGATTTCC[A/G]TAGTAAATATAATGT | 23607 |
rs776097283 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47530900 | TTGTGGACATATATT[G/T]CCAGAACTTATTTAC | 23607 |
rs776107871 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47570771 | AGATTGGGCAAATAT[A/G]ATGGAGGGGGCAAGA | 23607 |
rs776187598 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47601275 | TTTGTGGAACAGGGT[A/G]TGAAAACATCTTATT | 23607 |
rs776230881 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47541966 | CTCTCCTTAGAGTCC[-/T]TGTATCACCAAATCC | 23607 |
rs776242797 | snp | A/G | 1.64963e-05 | 0.00287192 | missense | CD2AP | GRCh38.p7 | 6:47574195 | TTTAAAGAAGGCTCT[A/G]TGAAACTTCGGACAA | 23607 |
rs776273427 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47518743 | CACATTTCACATTTC[C/T]ATCAGCAATGTATGA | 23607 |
rs776277036 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47565731 | TTGTCAAAAAATGTT[C/T]AGAATCTATTTTCTT | 23607 |
rs776297606 | in-del | -/A | 4.96151e-05 | 0.00498047 | frameshift-variant | CD2AP | GRCh38.p7 | 6:47576557 | TGGGACCCAAAACTC[-/A]AGAGTGTGGAGATAA | 23607 |
rs776343674 | in-del | -/TTTTTTTTTTT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47505012 | GGCTGTGGCAGTTTC[-/TTTTTTTTTTT]TTTTTTTTTTTTTTA | 23607 |
rs776344039 | in-del | -/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47558770 | TTCATCAGGGATATT[-/G]GCCTGAAATTTTCTT | 23607 |
rs776345948 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47588261 | TTACATATTAGTTTA[G/T]ATGTTTGTTTTGGGA | 23607 |
rs776355105 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47526014 | AGGAAAGGAAGTGAT[A/G]TTGGTAGGAAATAAA | 23607 |
rs776375579 | snp | C/G | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520079 | TGTTTAGAAAAATGA[C/G]CTGTGGAAATGATTT | 23607 |
rs776409563 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47532626 | TCAGTACTGTCTTTA[C/T]GCCAGTAGCACATTG | 23607 |
rs776427081 | snp | G/T | 1.67528e-05 | 0.00289415 | intron-variant | CD2AP | GRCh38.p7 | 6:47609355 | TAACCCATGCATAAA[G/T]AATTTTTTTCAAACC | 23607 |
rs776439752 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47622641 | GTGTGTTCGGGAGAG[A/G]AGGGTCTCCCTTTCT | 23607 |
rs776473074 | snp | A/T | 1.66065e-05 | 0.00288149 | missense | CD2AP | GRCh38.p7 | 6:47533729 | GAGGAATTCAGCCAC[A/T]TCCACAAACCAAAAA | 23607 |
rs776480336 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47526592 | TTCTAGATCTTGAGC[-/A]ATGAATTCATATATC | 23607 |
rs776488418 | snp | A/G | 1.65976e-05 | 0.00288072 | missense | CD2AP | GRCh38.p7 | 6:47533648 | ACAGTTTGCCCATCA[A/G]ACGGGAAAGGCATGG | 23607 |
rs776507914 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47575111 | TGAAGAGTTGGGTTC[A/C]GGAAAGAGAACTTCC | 23607 |
rs776508783 | snp | C/T | 1.64819e-05 | 0.00287066 | intron-variant | CD2AP | GRCh38.p7 | 6:47579352 | AAAAAAAAAAAAGGT[C/T]TATTGTCTTAATTAT | 23607 |
rs776516012 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47596415 | CACATCTTCCCACTC[C/T]CCTCCAACTCACAAC | 23607 |
rs776537571 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47623348 | AGGCCTATATATTTC[C/T]TCATGCAGGGAAAGG | 23607 |
rs776548986 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47570205 | CCGTTTTTCTCCAAA[C/G]AAGTAATTGCATTTT | 23607 |
rs776558624 | snp | A/G | 1.65141e-05 | 0.00287346 | missense | CD2AP | GRCh38.p7 | 6:47577026 | AAAGAATATTGTAGA[A/G]CATTATTTGCCTATG | 23607 |
rs776561104 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47562411 | ATCTAATGATGAGAG[C/T]TAGGAATAATGAGAT | 23607 |
rs776576072 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47503804 | TTGTGAAATAGTTAT[A/G]ACAGATAGTAGCCCC | 23607 |
rs776597780 | in-del | -/T | 1.78688e-05 | 0.00298899 | intron-variant | CD2AP | GRCh38.p7 | 6:47624166 | TTTATGTTTGCTCAA[-/T]TTTATGTTTTTTGTT | 23607 |
rs776607846 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47587338 | AGCTACTTAGAAACC[A/G]TGAAACTGATCACCC | 23607 |
rs776619472 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47487788 | CATTGATGCTGGAGA[C/T]CATATCACTTATTTT | 23607 |
rs776638684 | snp | A/C | 1.68332e-05 | 0.00290109 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47606172 | TTTTCTAGATGTTGT[A/C]AATTTTGATGACATA | 23607 |
rs776641440 | snp | C/T | 3.33067e-05 | 0.00408072 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47606274 | TTTCAATGGTGGACA[C/T]TCTGTGAGTTCATCT | 23607 |
rs776664622 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47514438 | AGACTAAAGTAGAGA[A/G]TAAAGATTTATTTGT | 23607 |
rs776670564 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47552395 | AGTGAGAACATACGA[C/T]GATTGGTTTTCCATT | 23607 |
rs776679863 | snp | C/T | 1.64955e-05 | 0.00287184 | intron-variant | CD2AP | GRCh38.p7 | 6:47574025 | TCAAGCGTTTTGTGA[C/T]TCTAGGTGTCATTCT | 23607 |
rs776773184 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47513614 | GAGACACCTTTACTA[C/T]TACTTTCTAATCTCT | 23607 |
rs776778555 | in-del | -/TA | 1.65094e-05 | 0.00287305 | frameshift-variant | CD2AP | GRCh38.p7 | 6:47503303 | ATTGTGGAGTATGAC[-/TA]TGATGCTGTACATGA | 23607 |
rs776805168 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47598151 | AGCATATGGAAAAAT[C/G]CTCAAAGTCACTAGT | 23607 |
rs776834111 | in-del | -/CT | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476213 | AAAGGCTCAGAAATA[-/CT]CTGTTTGCATATCCA | 23607 |
rs776839470 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47621007 | GTGACAGTTTGACTT[C/T]CTCTTTATTGATTTG | 23607 |
rs776841731 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47609357 | ACCCATGCATAAAGA[A/G]TTTTTTTCAAACCAT | 23607 |
rs776865224 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47567268 | TAGTAATATGTGCGT[A/G]TACTAGCATTTCTCA | 23607 |
rs776894469 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47525933 | AGAGTTTGCTTTGAC[C/T]ATACATGATTGCTTT | 23607 |
rs776917467 | in-del | -/AC | | | intron-variant | CD2AP | GRCh38.p7 | 6:47587819 | TTCCTATACACACAT[-/AC]ACAGTCATACCCACA | 23607 |
rs776930343 | snp | A/G | 1.65729e-05 | 0.00287857 | missense | CD2AP | GRCh38.p7 | 6:47554731 | AATTAGAGGTAACAG[A/G]TGATGGTGAAACTCA | 23607 |
rs776941589 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47481288 | GGCGGTGAACTTTTT[A/T]GTTTATTTTATAGGC | 23607 |
rs776946466 | snp | A/G | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624789 | TGTGCCTGTTTGTCT[A/G]CAATGCTGTTTATAT | 23607 |
rs776946658 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47593802 | CCCAGCAGTTCCAAA[C/T]GTCCAAGAGAATTGA | 23607 |
rs776951885 | snp | C/T | 3.30453e-05 | 0.00406467 | intron-variant | CD2AP | GRCh38.p7 | 6:47580920 | GTAAGAAGCATATTA[C/T]TCAGTTTGCTATTTT | 23607 |
rs776955329 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47561612 | ACATACAATCCCATA[C/T]CTCTACCCATATGTC | 23607 |
rs776978354 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47569214 | CTTGACATACTAATG[A/G]CTGACAAGTAGGAGA | 23607 |
rs776996395 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47556165 | GCACCTATCAACCCG[A/T]CATCTACATTAGGTA | 23607 |
rs777032933 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47605514 | TCTTTTTTTTTTGGT[A/G]TCTGATTTGCCTTAG | 23607 |
rs777059979 | snp | C/G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47499781 | AGAGTCTTGCTCTGT[C/G/T]GCAGTGGCACGACCT | 23607 |
rs777080236 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47585302 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAGG | 23607 |
rs777086130 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47518072 | GTTGGGGGAGGTTCT[G/T]AGTGTGTGTCTTTAA | 23607 |
rs777102694 | snp | C/T | 1.66394e-05 | 0.00288434 | missense | CD2AP | GRCh38.p7 | 6:47609144 | GTGTACCTTTCAACA[C/T]CTTCCAGTGCTTCTA | 23607 |
rs777108206 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47508691 | CTGGGATTACAGGGG[C/T]GTGCCACCACGCCCA | 23607 |
rs777122961 | snp | A/C | 1.65318e-05 | 0.002875 | missense | CD2AP | GRCh38.p7 | 6:47582037 | AGCTGCAGAGAAGAA[A/C]TATTTTTCTTTAAAG | 23607 |
rs777127972 | snp | A/G | 4.95013e-05 | 0.00497475 | intron-variant | CD2AP | GRCh38.p7 | 6:47574016 | GACAGGATGTCAAGC[A/G]TTTTGTGATTCTAGG | 23607 |
rs777174289 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47568148 | GCTTTGTAAGATGGA[A/G]ATGTCATTTGCAGAG | 23607 |
rs777215970 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47544771 | TGGATTTTAGAAAAA[A/T]TAATTGTAAGAATAT | 23607 |
rs777222983 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47481853 | GCATGATCATAGCTC[A/G]CTGCAGCCTCAAACT | 23607 |
rs777223356 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47516076 | TTGCTGAAAACCAAG[A/G]TTTTATTATACAGTT | 23607 |
rs777226576 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47534162 | TTTCCAAGGTGGTTG[G/T]CCTTGCAAATTACCT | 23607 |
rs777243678 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47559476 | TATGTTGACCAGACA[G/T]GTTTTGGACTCTTGG | 23607 |
rs777261794 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47620036 | TTTACTCTGTTGACT[C/G]TTCCATTTGCCATGC | 23607 |
rs777333648 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47561044 | ATCAGGTATCAGTCT[A/G]TTACCAGTATTATTT | 23607 |
rs777342185 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47539755 | AATGCAGTATGTCCC[C/T]GCCTTTGCTGTACCT | 23607 |
rs777344178 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47571368 | ACTGCACAGGACTGG[C/T]ATTCCTGAGAAAAGG | 23607 |
rs777410748 | snp | A/G | 3.31038e-05 | 0.00406827 | intron-variant | CD2AP | GRCh38.p7 | 6:47576977 | AATGAATCCATTTGT[A/G]TGAGCCACATTATTT | 23607 |
rs777434963 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47567564 | AAATATTTGTTACAG[A/G]AAAGGGTGCAATAAA | 23607 |
rs777440553 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47622092 | GGAATATGGCTGCCT[A/G]TGCTGAATCATGCTG | 23607 |
rs777463857 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47568844 | CTGGGATGGAATCCT[C/G]TGTAGTGACATTTAA | 23607 |
rs777465765 | snp | A/T | 4.87009e-05 | 0.00493438 | intron-variant | CD2AP | GRCh38.p7 | 6:47599475 | AGCGGTGGTGCATTT[A/T]AAAAAAAAAATTGTC | 23607 |
rs777466357 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47537797 | TGCTAAGGATGAGAA[-/T]TTTTTTTTTTTTTGG | 23607 |
rs777475480 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47485073 | TAAAAGTATAGCATG[C/T]ACATACATTTATATG | 23607 |
rs777487362 | snp | C/T | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624229 | TCCTGTCTTCTTGAG[C/T]GGTGTGGACCTGGTG | 23607 |
rs777493828 | snp | A/T | | | missense | CD2AP | GRCh38.p7 | 6:47607949 | ACAGCCCCGAAAAAA[A/T]CTTGAAGTTACCAAA | 23607 |
rs777510538 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47537410 | TCATCTTGGGGTTAG[A/C]ACACCCTACCCTCTT | 23607 |
rs777512458 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47524119 | AAACCATGTTAATGT[C/T]TGCCTTGGACTTAAT | 23607 |
rs777516106 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47511414 | AGGAGACATAATAAC[C/T]AAATACATTTTGGTT | 23607 |
rs777528378 | in-del | -/TGGGAC | 1.64969e-05 | 0.00287196 | cds-indel | CD2AP | GRCh38.p7 | 6:47554686 | CCCTGAATAACAAGT[-/TGGGAC]TGTTTCCCTCAAATT | 23607 |
rs777540735 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47595436 | TAAATTTGAATGTTA[C/T]ATAGGACTTGAGTTT | 23607 |
rs777582601 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47619191 | GAGCAGTATATACTG[C/T]ACCACGTTCGTAGTC | 23607 |
rs777594823 | snp | A/G | 1.66366e-05 | 0.0028841 | intron-variant | CD2AP | GRCh38.p7 | 6:47544720 | AGGTAAGGAAAAAAT[A/G]TGTTACAGGTAAAAC | 23607 |
rs777609568 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47517345 | GGGAGTGCAGTGGTG[C/T]GGTGCGATCACAGCT | 23607 |
rs777614355 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47566795 | CAGAGGATATGATCT[C/T]ATTCCTTTTTATGGC | 23607 |
rs777620356 | snp | A/G | 3.29804e-05 | 0.00406068 | missense | CD2AP | GRCh38.p7 | 6:47554664 | GAAGAAGGCTGGTGG[A/G]GTGGAACCCTGAATA | 23607 |
rs777629761 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47546033 | ACCTGAAAAAGAATT[C/G]AGAAGGTAAGTTATT | 23607 |
rs777636337 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47583541 | CCTTTTCAAATTGGC[A/G]TCTTTCACTTAATTA | 23607 |
rs777657427 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47558936 | TGGTAGAGTTCGGCT[A/G]TGAATCCATCTAGAG | 23607 |
rs777670375 | snp | C/T | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476424 | ACCCCCCTAGAAGAA[C/T]GCAAAATCTCTGAGG | 23607 |
rs777671290 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47519838 | AAAAAGGCAGAACTT[C/T]TCAAATTGCCCTTTT | 23607 |
rs777673676 | snp | C/T | 1.65762e-05 | 0.00287886 | intron-variant | CD2AP | GRCh38.p7 | 6:47581972 | CTTTAAAACTGTCTT[C/T]TTAAAAAAGTATTAA | 23607 |
rs777711947 | snp | A/G | 1.65083e-05 | 0.00287296 | missense | CD2AP | GRCh38.p7 | 6:47503304 | TTGTGGAGTATGACT[A/G]TGATGCTGTACATGA | 23607 |
rs777763877 | in-del | -/GTATTTCGCA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47494588 | GTTGTATTTCGCAGT[-/GTATTTCGCA]GGTTACTTTTCTTTT | 23607 |
rs777815288 | snp | A/T | 2.1679e-05 | 0.00329227 | intron-variant | CD2AP | GRCh38.p7 | 6:47609109 | AATCAGAAATTTTTT[A/T]TTTACGTTTTCAGCC | 23607 |
rs777861120 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47622416 | TCCTTCTCCCTGTGG[A/C]GTTTTACCCCCTGCT | 23607 |
rs777870212 | snp | A/T | 1.68074e-05 | 0.00289887 | intron-variant | CD2AP | GRCh38.p7 | 6:47608047 | AGGTGCATTGTGGTC[A/T]AAGGTTTGTTGACTT | 23607 |
rs777878128 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47555277 | ACCATTTAAGAGTAT[A/G]ATTGACAAAATTTTA | 23607 |
rs777886865 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47526864 | ATGAGCAAGTACTCT[C/T]TGGCATGTTGAGGTT | 23607 |
rs777886880 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47540066 | TGAGCGCCTGTGGTC[C/T]CAGCTACTTGAGAGG | 23607 |
rs777889581 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47560503 | TTTTGTTTTCTTGAC[A/G]TTGACATTTTTGAAG | 23607 |
rs777893903 | in-del | -/ACTGA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47534916 | TTCCCATTTCAGGCT[-/ACTGA]ACTGAGTAGCTGTGA | 23607 |
rs777897093 | snp | G/T | | | synonymous-codon | CD2AP | GRCh38.p7 | 6:47580896 | ACCTCCTGCTAAGGC[G/T]CCAGGTATGTAAGAA | 23607 |
rs777903768 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47589264 | AAGTTAGGTATTAAA[C/T]TTACAGGTATGGGTA | 23607 |
rs777904060 | snp | G/T | 1.65389e-05 | 0.00287562 | missense | CD2AP | GRCh38.p7 | 6:47574251 | GAAAAAACCAGAAAA[G/T]GTGGTAATGATGGAC | 23607 |
rs777904165 | in-del | -/TGTATATATA | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624720 | GTGTGTGTGTGTGTG[-/TGTATATATA]TATATATATTTTTAC | 23607 |
rs777910584 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47561520 | GGCATCAAGATCTGG[G/T]TAGAGGTGTGGTCAT | 23607 |
rs777922110 | snp | C/T | 1.71773e-05 | 0.00293059 | intron-variant | CD2AP | GRCh38.p7 | 6:47478277 | GCGCTTCCCGCCGCC[C/T]GTCCGGACCTTCCAG | 23607 |
rs777932991 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47597967 | CCACATGCAGCAGTA[A/G]TCAAGGAATGGCAGC | 23607 |
rs778035707 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47499365 | ACATACATGTATACA[C/T]ATATCTGTTTATTTC | 23607 |
rs778036028 | snp | C/G | 1.74342e-05 | 0.00295242 | missense | CD2AP | GRCh38.p7 | 6:47612507 | CGAAAAGATTTGGAA[C/G]AAGAGAAGACAATGA | 23607 |
rs778096477 | snp | A/T | 3.58327e-05 | 0.00423262 | intron-variant | CD2AP | GRCh38.p7 | 6:47599261 | AAAAAAAAGTCGTGT[A/T]TCATACTAGTGATTT | 23607 |
rs778101485 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47577273 | TAATAAGTGCTCAGA[A/G]CGTTCTCTTTTTGAG | 23607 |
rs778131415 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47584002 | TTCAGTTGCAATTCC[A/G]TAATGATATATGATG | 23607 |
rs778136445 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47506500 | ACGCCACTGCACTCC[A/G]GCCTGGGCACCATTG | 23607 |
rs778150733 | in-del | -/TG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47619309 | GCTCCCACATGTCCA[-/TG]AGAACATACAATGTT | 23607 |
rs778162633 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47515168 | ATAAAAAGATAATTA[A/G]GCAGACTACTTTGGC | 23607 |
rs778165812 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47507697 | TGATCTGCCCGCCTT[A/G]GCCTCAGAAAATGCA | 23607 |
rs778167014 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47508536 | ACTTTCTTTCTTTCT[-/T]TTTTTTTTTGTTTTT | 23607 |
rs778196015 | in-del | -/GT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47533228 | TGGTTGCAACAGAAA[-/GT]GTATGGTCTGCAAAT | 23607 |
rs778236695 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47563444 | CTTGAAGAGGCAGGG[-/A]AAAAGAAGGATGGCT | 23607 |
rs778263929 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47563393 | TCAGAAATGTCACAG[A/G]AAACATTAGAAAATA | 23607 |
rs778296103 | snp | G/T | 1.65754e-05 | 0.00287879 | intron-variant | CD2AP | GRCh38.p7 | 6:47609329 | CCTTCTTTTCTCCTG[G/T]GAGTACTACTTAACC | 23607 |
rs778306814 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47550577 | ACAGGGAACAGTTCT[A/G]TACTTCTGGTGGGAA | 23607 |
rs778326186 | in-del | -/AAG/AG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47579339 | ACTTTATCTTAAAAA[-/AAG/AG]AAAAAAAAAGGTCTA | 23607 |
rs778334448 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47523866 | TTTTAAATCACAGAC[A/G]TAGTATATGTTGAAA | 23607 |
rs778353969 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47548281 | TGGTTCTTTGAAAAG[A/G]TAAATAAGATTGATA | 23607 |
rs778386276 | snp | A/T | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626503 | AGCATGGAATCTCAT[A/T]GCCAAATTATTAGTG | 23607 |
rs778386630 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47562132 | TAAACATCGCAAGCT[A/G]CAATTGTGTTGCCTT | 23607 |
rs778401042 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47571587 | ACTATATGTAGAGAG[C/T]GCACCAGAACTGTTC | 23607 |
rs778414858 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47492492 | CAAGTAGCTAGGACT[A/G]TAGGTGCTGCCCCAC | 23607 |
rs778470483 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47545868 | TGAACAGCCTTGAGC[C/G]CTACACTTCCCTCTG | 23607 |
rs778481750 | snp | G/T | 1.65168e-05 | 0.00287369 | missense | CD2AP | GRCh38.p7 | 6:47579406 | GGAGAAGCTGGCTGG[G/T]GGAGGGGCGAACTTA | 23607 |
rs778525256 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | CD2AP | GRCh38.p7 | 6:47627161 | AGTCTTTATTGGTTA[C/T]TTTTTGTTAACTTTA | 23607 |
rs778567682 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47535210 | CTGCTGTTCAAGGTC[A/G]TTGCCAAGGTCTGAT | 23607 |
rs778585390 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47543740 | ATTTACCACCCCCAC[A/G]AAGGCACTATTGCCA | 23607 |
rs778585546 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47580669 | TTTGACCAATGAGGC[A/T]GTTTTTTCTAATGAA | 23607 |
rs778609069 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47607844 | GAAAATCCATAAAAG[G/T]TATTTGCTTTATTAT | 23607 |
rs778619135 | in-del | -/TGTGTGTAT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47491264 | TCTTCCTGATATGTG[-/TGTGTGTAT]GTGTGTGTGTGTGTG | 23607 |
rs778655483 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47522483 | ATATGTTAACAGAAG[C/G]TGTCTCAGGTGCTGG | 23607 |
rs778682478 | in-del | -/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47574827 | TATAAGAACTAAAAA[-/G]AGGCTTTAAAATAAA | 23607 |
rs778709158 | snp | A/G | | | | | GRCh38.p7 | 6:47483007 | GTAAACTGATGAAGC[A/G]AGTTGTGAAAGATCT | 23607 |
rs778741477 | snp | A/G | | | | | GRCh38.p7 | 6:47544505 | ATACGTTCTGTTTTT[A/G]TTTATTTATATAAGT | 23607 |
rs778764132 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47579043 | TTTTTAAAACTAAAC[A/G]CAATTTTGTAACTGC | 23607 |
rs778781978 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47602728 | ACCGTGTCTCTACAG[-/A]AAAAAAAAAAAAAAG | 23607 |
rs778783275 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47622421 | CTCCCTGTGGAGTTT[A/T]ACCCCCTGCTTCTCT | 23607 |
rs778813991 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47511241 | CCCTTCACCTTTGTG[G/T]TATTCTTCCCCAAAG | 23607 |
rs778831179 | in-del | -/GTC | | | intron-variant | CD2AP | GRCh38.p7 | 6:47597788 | AAGGCAGGTACTGGT[-/GTC]GTCGTGGAGTTTGGG | 23607 |
rs778874856 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47564424 | CTAATTTATATTTGA[A/C]TTTAGTTCATTACTT | 23607 |
rs778875298 | in-del | -/AAG | | | cds-indel | CD2AP | GRCh38.p7 | 6:47579428 | GCGAACTTAATGGTA[-/AAG]AAGGAGTATTTCCAG | 23607 |
rs778896932 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47494836 | ATGTCTGAGTCTTAG[A/C]CCTTCATACGTGTAA | 23607 |
rs778926482 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47483772 | TTCTGTTTATTTGGT[C/T]CCAGGGATTTGATGT | 23607 |
rs778949333 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47577814 | AACTCTTGAGCTCAA[G/T]CATTCCTCTCGCTTT | 23607 |
rs778959881 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47566590 | TTCCTGCACCTATCG[A/G]CCCATCCTCTCAATT | 23607 |
rs778963265 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47605501 | ATGTAGCTTTTTCTC[-/T]TTTTTTTTTGGTATC | 23607 |
rs778967263 | in-del | -/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47481033 | AATGCCTATTGAGAA[-/G]TTTGAGGTATTCTGT | 23607 |
rs778976053 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47478912 | TTTGGAGTTAGACTT[C/T]CTTGCCGGAGGAGAG | 23607 |
rs779007301 | in-del | -/AT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47491282 | TGTATGTGTGTGTGT[-/AT]GTGTGTGTGTGTGTG | 23607 |
rs779026902 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47537636 | AATACATTACCTCTG[A/T]TCACATTATCTTTTT | 23607 |
rs779036699 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47553282 | GAAATAAATCTTTTT[C/G]TAGCTATATTGTGTG | 23607 |
rs779040688 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47592707 | TAAAAACCCTAAACA[A/G]CAGAGTTTAGAGAGC | 23607 |
rs779043720 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47536006 | AACACTGGATGTAAA[C/T]TCTTTTCTCTTGTAA | 23607 |
rs779054962 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47587324 | GGGGCGCAGAAAAGA[A/G]CTACTTAGAAACCAT | 23607 |
rs779061496 | snp | C/T | 3.29598e-05 | 0.00405941 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47503353 | AGTTGGAGAAATCAT[C/T]AGGAATGTGAAAAAG | 23607 |
rs779070731 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47587997 | TCTGATTCCCAGTCA[C/G]TGGATGGATTTATTT | 23607 |
rs779120976 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47617327 | ATCCTTGGCTTTTCT[C/G]TTTGAGCATTCACAT | 23607 |
rs779122248 | snp | C/G | 4.96192e-05 | 0.00498067 | intron-variant | CD2AP | GRCh38.p7 | 6:47581996 | GTATTAATGTTTTTT[C/G]CCATAGCTCCAAAGC | 23607 |
rs779152482 | in-del | -/TGAAAGAACA | 1.72786e-05 | 0.00293922 | intron-variant | CD2AP | GRCh38.p7 | 6:47579522 | AATGATGATAATACT[-/TGAAAGAACA]TTTTGCCACTATTCT | 23607 |
rs779174200 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47600910 | ATTTTCACAAATTTG[A/G]GGGATCTTTATCACA | 23607 |
rs779193266 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47514286 | ATTGATCTTTTTTAA[C/G]TCATTTCATTTTTAT | 23607 |
rs779206166 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47518046 | TTTGTAAAACTTTTG[G/T]GTCAGGTGTTGTTGG | 23607 |
rs779226333 | snp | A/G | 1.68618e-05 | 0.00290356 | intron-variant | CD2AP | GRCh38.p7 | 6:47608055 | TGTGGTCTAAGGTTT[A/G]TTGACTTTCTGGGAT | 23607 |
rs779240259 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47617023 | CCCAGGCTAGAGTAC[A/G]GTGACACAATCATAG | 23607 |
rs779242012 | snp | A/G | 3.31055e-05 | 0.00406837 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47576535 | CTAGCCCTTAATCCT[A/G]CAGTCACTGGGACCC | 23607 |
rs779273145 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47524803 | GGAGAGCAATTGTGT[-/A]ACAAAAAGCATAGTA | 23607 |
rs779289327 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47488626 | ACATTTCAAGTGCTC[A/G]ATATTTTTTGATTAT | 23607 |
rs779295575 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47624092 | AAAAAGTCTGAAGGC[C/T]TGAAAGTATGATCAC | 23607 |
rs779327097 | snp | A/G | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47626176 | TTTTCTCAATAGTAC[A/G]TGAAATCAAGATGCT | 23607 |
rs779329962 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47538741 | ATTTGATGGAAACAT[A/T]AAAAACAGTCTTCAG | 23607 |
rs779379965 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47501518 | AGGGTCTCAAAATAC[C/T]GAACAGAATTAAGGT | 23607 |
rs779380266 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47527578 | TGGACACAGTGCACC[A/G]TAATGAATGAATTGA | 23607 |
rs779398744 | in-del | -/AA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47614889 | CTCCCATTTAAACTT[-/AA]GAGTTTATCTTAATT | 23607 |
rs779403986 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47549070 | AGTGTAATAAAAGCC[A/G]TCTATGCAAAACCAC | 23607 |
rs779404116 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47561241 | GTACAGAACATTTCC[A/G]TCACCCCCAAAATAT | 23607 |
rs779406395 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47575753 | TCCTTTACAGATTAC[A/G]ATGGAAAAATGTCTA | 23607 |
rs779431948 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47497776 | TCTAATCATCTTTAG[-/T]TTTTTTGTCCTTAAC | 23607 |
rs779459053 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47487266 | TGCGTGTCAAATGGA[A/G]ATAAAAGGCTGTGTT | 23607 |
rs779479526 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47614986 | CTAATGTTTATGTTC[A/G]TTTGCATTATTCTTT | 23607 |
rs779485362 | snp | A/G | 1.76965e-05 | 0.00297454 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47612524 | AGAGAAGACAATGAG[A/G]AGTAATCTAGAGGTA | 23607 |
rs779504309 | snp | G/T | 3.29707e-05 | 0.00406008 | missense | CD2AP | GRCh38.p7 | 6:47579424 | AGGGGCGAACTTAAT[G/T]GTAAAGAAGGAGTAT | 23607 |
rs779559642 | in-del | -/GCT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47482972 | TGAGAATTGGGTGGA[-/GCT]GCAGACCTGTTTCTT | 23607 |
rs779581496 | snp | C/T | 1.6492e-05 | 0.00287154 | missense | CD2AP | GRCh38.p7 | 6:47544666 | AAAATGAGGATGAAC[C/T]GGAGCTGAAAGTGGG | 23607 |
rs779599186 | snp | A/G | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521239 | ATACTCATAATTATA[A/G]AAGTTCTTTTCTATT | 23607 |
rs779629644 | in-del | -/AAGG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47614419 | TCTATCTCAGATAAT[-/AAGG]AAGGCCAAGTAGAGG | 23607 |
rs779663550 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47481698 | AGATGATATATGCAC[G/T]TCTATAATAGAGTGA | 23607 |
rs779677962 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47561987 | TGTTAGCCAAGATGG[G/T]CTCAATGACCTCGTG | 23607 |
rs779683099 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47612309 | AACTGTTATATTGAA[A/C]CATTCTAACTAGAGA | 23607 |
rs779704748 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47547852 | CAGCGAAATAAAACT[A/G]GAAATCAACTCCAAA | 23607 |
rs779705017 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47587611 | GCTTTTTGAGATGTC[C/T]TTTTTTGTATTTATC | 23607 |
rs779712608 | in-del | -/A | 3.30327e-05 | 0.0040639 | frameshift-variant | CD2AP | GRCh38.p7 | 6:47608000 | GAAGCCATCTGAATT[-/A]AAAAAAAGATACATG | 23607 |
rs779741663 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47543759 | GCACTATTGCCAGAC[-/A]CATTGGGTGTTAGGG | 23607 |
rs779751864 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47515105 | GGTAGAAAGTTATAG[G/T]AGTACTGAGTGCATT | 23607 |
rs779827500 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47591070 | CACAAATGTTCAACA[G/T]CAAAAGAATGGGTAA | 23607 |
rs779842975 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47577506 | AGGGAAACAAGCTAA[A/G]CATCCATGAGTATGG | 23607 |
rs779860972 | snp | A/G | 4.97806e-05 | 0.00498877 | missense | CD2AP | GRCh38.p7 | 6:47606258 | GAAGGTTGCCGGGCC[A/G]TTTCAATGGTGGACA | 23607 |
rs779882646 | snp | A/T | 1.67494e-05 | 0.00289386 | intron-variant | CD2AP | GRCh38.p7 | 6:47577141 | TGAATTGCTTAATTT[A/T]TTTATAGAAATATTT | 23607 |
rs779897846 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47522333 | GACAGTATTTGTTGA[C/T]AAGGGGATTCAATCT | 23607 |
rs779919838 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47623928 | TACAGCTTTAATTTT[A/T]AATGCTCACATGACT | 23607 |
rs779938021 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47492971 | CAGCTTTAAATAACA[C/T]TGCAACACTTCATGT | 23607 |
rs779950349 | in-del | -/ACTT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47551136 | AATCACCACTAAAGA[-/ACTT]ACTTATGTAACCTAA | 23607 |
rs779987473 | snp | A/C | 1.64936e-05 | 0.00287168 | missense | CD2AP | GRCh38.p7 | 6:47595927 | TCCCACCCAAGAAAC[A/C]TACTCCACCTACCAA | 23607 |
rs779998902 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47569866 | CTTATACTCCTCCTG[C/G]TGAGCAGCTTTGCAA | 23607 |
rs780007682 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47575855 | TTTTTTTTTCTCCTC[-/T]TTTCATTTTAAGGTT | 23607 |
rs780015226 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47538923 | ACTGAGTCTGAAATT[C/T]CACACAATTTGGTTT | 23607 |
rs780020065 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47525734 | ACCATTTGCATATGT[A/T]TTTCAGTTTTTATCC | 23607 |
rs780031526 | in-del | -/CAT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47593517 | TGAAAAGATGTTTAA[-/CAT]CATTAATCATGTCAG | 23607 |
rs780068287 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47536929 | ATGTTTCACTTTACA[C/T]TTGGAAGAAACTGAT | 23607 |
rs780075183 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47551252 | ATTTGAAGGAGTATT[A/G]AAGTTTAATTTCACA | 23607 |
rs780094912 | snp | A/T | 1.65293e-05 | 0.00287479 | missense | CD2AP | GRCh38.p7 | 6:47582015 | TAGCTCCAAAGCCTG[A/T]ACTGATAGCTGCAGA | 23607 |
rs780097102 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47555734 | AGGTGTTAGTCTTCC[A/G]TGATGGCAGAAAACT | 23607 |
rs780107960 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47566048 | GGAACATTCCTCTCT[C/T]ACAGCCTTTGTGCTT | 23607 |
rs780111596 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47482935 | TAGGTAGAGAAAGAA[A/G]TATAATGATTATTCA | 23607 |
rs780125183 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47494551 | CCCTTGGAGTGTAGG[C/G]CTTTGTTACAGAGAA | 23607 |
rs780129555 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47484258 | ATGCTGTACTCATTT[G/T]TGAATCATAACCTTG | 23607 |
rs780145207 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47478749 | TTCCTGCTGAAACTC[G/T]CAAGGGGTGCCTCAA | 23607 |
rs780155889 | snp | A/G | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476909 | GTGCTGGATGACTGA[A/G]AATTACAAAATTTCT | 23607 |
rs780172298 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47516442 | GTGTACTATCAAAGG[A/G]GCAGAAAAATATGAT | 23607 |
rs780174128 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47616217 | CTGCCTCAGCCTCCC[A/G]GGTAGCTAGGACTGT | 23607 |
rs780186024 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47550679 | TGATCCAGCAATCCC[A/C]CTACAATCCCAGAGG | 23607 |
rs780189676 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47582489 | GGAAAGTTATTCCAG[A/G]GTACCACATGTATTT | 23607 |
rs780228475 | snp | A/G | 1.67716e-05 | 0.00289578 | intron-variant | CD2AP | GRCh38.p7 | 6:47595826 | ACCTAAATAATTTTG[A/G]TTGTTAATAACTTGT | 23607 |
rs780231869 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47517982 | GATAGGAGTGAAGTT[A/G]AATAGAAAATGTCAG | 23607 |
rs780246981 | snp | A/C | 2.36169e-05 | 0.00343626 | intron-variant | CD2AP | GRCh38.p7 | 6:47533555 | TTGAGGATTTAATAT[A/C]AAAAATATAACTTAA | 23607 |
rs780252546 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47570542 | TGCTCCTTATCCTCT[-/T]TTCTTCTTTCCAGTG | 23607 |
rs780272900 | snp | C/T | 7.30807e-05 | 0.00604442 | intron-variant | CD2AP | GRCh38.p7 | 6:47554818 | AAACTTTATATAGCA[C/T]CTAGTGTTTTATTTT | 23607 |
rs780275518 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47572063 | TTTCTGCTAACTAGA[A/T]GTCAGTAACACTCCC | 23607 |
rs780282108 | snp | A/T | 1.64996e-05 | 0.0028722 | missense | CD2AP | GRCh38.p7 | 6:47609220 | AAGTGGAAACAGATG[A/T]TGTGAAAAAAAATTC | 23607 |
rs780290842 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47578749 | GCAGCCTCTGCCTCC[C/T]GAGTTCAAGCAATTC | 23607 |
rs780326084 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47600589 | GCTATATTTACTACT[A/G]ATTTCTGGGAATTGA | 23607 |
rs780336709 | snp | C/T | 1.66629e-05 | 0.00288638 | intron-variant | CD2AP | GRCh38.p7 | 6:47576645 | TGGGAATAGTAGAAA[C/T]ATACTCAAATGTATT | 23607 |
rs780342498 | in-del | -/AA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47549459 | CTTTTACAATAGCTG[-/AA]CAAAAAAAAAAAAAA | 23607 |
rs780361053 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47544365 | TTTGGATATTTTGCT[C/T]TTGTGTAAATGGTGG | 23607 |
rs780369760 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47596183 | GTGTATTTATTGTAT[A/G]CAACATGATGTTTTA | 23607 |
rs780373548 | snp | C/G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47551884 | TTACAGTGTAGGCAT[C/G/T]TCAAGGTCGTCGGAC | 23607 |
rs780380685 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47622855 | TCTTGCCTCCTGTCC[G/T]CCATGATGATCCCTG | 23607 |
rs780433962 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47623825 | TTTACTGTTGTTTAT[A/G]TATCCTTTGTTTAAT | 23607 |
rs780434088 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47609415 | GGTGTGGTAGTTCGC[A/G]CCTGTAATCCCAGCA | 23607 |
rs780437002 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47504202 | AATTGTCTTGTTTTC[C/T]GTGTATTAGTTTTCT | 23607 |
rs780521436 | snp | C/T | 3.29674e-05 | 0.00405988 | missense | CD2AP | GRCh38.p7 | 6:47503400 | GGCTGGAAGGAGAAC[C/T]AAATGGGAGAAGAGG | 23607 |
rs780529533 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47538586 | GACTAATTAAATAAA[G/T]TTTAATGCTTTAATA | 23607 |
rs780544226 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47485323 | ATGGAAGACAGTGAT[A/G]TTGATGATCCTGATC | 23607 |
rs780545300 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47561841 | GCTGGAGTGCAGTGG[C/T]GCGATCTTGGCTCAC | 23607 |
rs780574436 | snp | C/G | 1.65411e-05 | 0.00287581 | missense | CD2AP | GRCh38.p7 | 6:47576548 | CTACAGTCACTGGGA[C/G]CCAAAACTCAGAGTG | 23607 |
rs780584177 | snp | A/G | 0.00030036 | 0.0122511 | intron-variant | CD2AP | GRCh38.p7 | 6:47582090 | ATTTTCAACTTTCAA[A/G]AAAGCAATTATTTCT | 23607 |
rs780642261 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47536791 | AGGTTGCAAGTCACA[-/T]TTACTTCTGACACCC | 23607 |
rs780656933 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47546099 | CCAGTTTAAGGAAAT[A/C]AAAAAAATGATACAA | 23607 |
rs780664723 | in-del | -/CTAT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47507441 | TGAGCAGAAGAATCA[-/CTAT]CTATGGCAGTGATAG | 23607 |
rs780669773 | snp | A/G | 1.77458e-05 | 0.00297868 | intron-variant | CD2AP | GRCh38.p7 | 6:47599463 | GTCAGCATGGACAGC[A/G]GTGGTGCATTTAAAA | 23607 |
rs780680934 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47592857 | AGCTGTATCCTTTAT[A/T]ATAAACTGTTAACAG | 23607 |
rs780705647 | snp | C/T | 1.64939e-05 | 0.0028717 | missense | CD2AP | GRCh38.p7 | 6:47554647 | GTGAACTTTTTCAGG[C/T]AGAAGAAGGCTGGTG | 23607 |
rs780732823 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47601732 | TCAAATACAGCCTCA[A/C]ATATAATGTGTGAAA | 23607 |
rs780744910 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47547592 | GTGGGGGACTTCAAT[A/G]CTCCACTGACAGCAT | 23607 |
rs780745527 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47495826 | CCCACAATTTTTGGC[A/G]TTTTTATGCTTTTTC | 23607 |
rs780748974 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47532543 | ATTTTAAGATTCCAT[A/C]TTTCCTCATTTTTTT | 23607 |
rs780759079 | snp | C/T | 1.65067e-05 | 0.00287282 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47544685 | GCTGAAAGTGGGAGA[C/T]ATTATTGATATTAAT | 23607 |
rs780772668 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47597171 | ATAGTACAAATCCAG[C/T]CAGGGTTGGAACCAT | 23607 |
rs780772741 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47559258 | CTCTGTTTCGTGCAA[-/T]TTTTTTTTTTTTTTT | 23607 |
rs780777654 | in-del | -/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47618327 | TGTCTCAAAAAAAAA[-/C]GAGTAGTCTTCCAAA | 23607 |
rs780812889 | in-del | -/TTGATTTTTCATC/TTGATTTTTCATCTAAGA/TTGATTTTTCATCTAAGATTTAAAA | 6.59341e-05 | 0.00574137 | frameshift-variant, cds-indel | CD2AP | GRCh38.p7 | 6:47595976 | TCTTCTGGAACAGTG[lengthTooLong]TACCCAAAGCGACCT | 23607 |
rs780841533 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47620495 | TGATGCCTCCAGATT[C/T]GTTCTTTTTCCTTAG | 23607 |
rs780856757 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47561132 | TTTTTAAAAAAGTCA[A/G]CTTTATTGGAGGTAC | 23607 |
rs780895089 | snp | A/G | 3.31417e-05 | 0.00407059 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47606250 | GCCTGGAAGAAGGTT[A/G]CCGGGCCGTTTCAAT | 23607 |
rs780902935 | snp | C/T | | | intron-variant, utr-variant-5-prime | CD2AP | GRCh38.p7 | 6:47522217 | GCAAGCGCCAGAGCA[C/T]AGAGAGTCATGGAAA | 23607 |
rs780941458 | snp | C/T | 1.86215e-05 | 0.00305129 | intron-variant | CD2AP | GRCh38.p7 | 6:47612552 | GTAATTAATTTCTTC[C/T]AGCATTGAGAGTTTA | 23607 |
rs780955376 | snp | A/G | 5.64382e-05 | 0.00531186 | intron-variant | CD2AP | GRCh38.p7 | 6:47533801 | ACATCAAAATAGAAG[A/G]ATATTTTATAACTGT | 23607 |
rs780986956 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47480480 | TAGGTGGTACAGCTA[C/G]AGAGTTAAAAGCATG | 23607 |
rs780993253 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47603011 | TATTTGATATTTGGT[A/G]GTTGATCTATTTTTT | 23607 |
rs781009773 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47583051 | GCCTTCCAAAGTGCT[A/G]GGATTACAGGTGTGA | 23607 |
rs781015116 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47514207 | TTTAGTATGTCATCA[A/G]TCTTTTTTTGTGTTT | 23607 |
rs781034305 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47604563 | AAAATGATTGGATTG[C/T]ACTTGTTAAGGTTTT | 23607 |
rs781043799 | in-del | -/A | 1.65556e-05 | 0.00287707 | frameshift-variant | CD2AP | GRCh38.p7 | 6:47607933 | TCATTTAGCCAACTC[-/A]ACAGCCCCGAAAAAA | 23607 |
rs781051303 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47533576 | TATAACTTAACTTGC[C/T]TCTTTATTTATTTTC | 23607 |
rs781090766 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47486900 | TTGGTTAGAGTGTTT[C/T]TGGGGGACATTTAAA | 23607 |
rs781103349 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47528192 | ACTTCTTTTGGGGGA[C/T]GAGACAGAGTCTCTT | 23607 |
rs781113188 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47554056 | TAGCTGGGACTACAG[A/G]CGCGAACCACCATGC | 23607 |
rs781129940 | snp | A/G | 6.60644e-05 | 0.00574698 | synonymous-codon | CD2AP | GRCh38.p7 | 6:47574227 | AACATCCAGTAGTGA[A/G]ACAGAAGAGAAAAAA | 23607 |
rs781175714 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47499027 | TGCTCAAAATGTCCT[C/G]ATTTGGCCAGTAAGA | 23607 |
rs781198577 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47619217 | TAGTCTTTCATCCCT[C/T]GCCCCCTTCCCACTC | 23607 |
rs781202667 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47481630 | GGATTACAGGCGTGA[A/G]CCACTGCACCTGGCC | 23607 |
rs781222671 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47540653 | AAATAAAGCTCTTGG[A/G]TAAAATATAACTAGG | 23607 |
rs781225141 | snp | A/G | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47520906 | TGCATTGGCATTTCT[A/G]TGTTGCAGACTTCTC | 23607 |
rs781225870 | snp | C/G | 0.000176819 | 0.00940097 | intron-variant | CD2AP | GRCh38.p7 | 6:47478269 | AGACTCGGGCGCTTC[C/G]CGCCGCCCGTCCGGA | 23607 |
rs781227070 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47583576 | CCTTTAAAATTTCTC[C/T]GTATGTTTTCATGGC | 23607 |
rs781228348 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47618745 | TTGCCATAAAAATTA[A/T]GACAAGAGTCAAATT | 23607 |
rs781238030 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47577396 | AATTAACCTCAACTT[A/C]CCAGGTTTTTATTCT | 23607 |
rs781238071 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47567773 | TATATAATTAGATGT[C/G]AATGTTGAGCCTGGA | 23607 |
rs781256344 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47578575 | AGTATATAAAGTGTT[A/G]AAAGTGTTAAGAAGG | 23607 |
rs781268447 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47530408 | AAACCATTTATCTGC[-/T]TTTTAATCTATACAT | 23607 |
rs781275179 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47514441 | CTAAAGTAGAGAATA[A/C]AGATTTATTTGTGGG | 23607 |
rs781287524 | snp | C/T | 8.34021e-05 | 0.0064571 | intron-variant | CD2AP | GRCh38.p7 | 6:47595848 | ATAACTTGTGAAATA[C/T]TTTAAATCTTAGATG | 23607 |
rs781303500 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47542745 | AATAAACCATATCAG[A/T]TACCTAGAATAAGCC | 23607 |
rs781320687 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47558745 | TTTATTGAGGATTTT[C/T]GCATTGATGTTCATC | 23607 |
rs781322618 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47527272 | GAAGAAGTATACCTG[A/T]TGTTGCTGCTCTTGG | 23607 |
rs781327060 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47585079 | TGGGCGGATCATGAG[G/T]TCAGGACATTGAGAC | 23607 |
rs781406571 | snp | G/T | 1.65004e-05 | 0.00287227 | intron-variant | CD2AP | GRCh38.p7 | 6:47609316 | ACGGGTAAGTAGCCC[G/T]TCTTTTCTCCTGTGA | 23607 |
rs781407068 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47585575 | GACCTCGATGTCCTA[C/T]AGAGTTGAGGATGCA | 23607 |
rs781417185 | in-del | -/GCCCAAGCT | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47477543 | CCAGACCAAACGCCC[-/GCCCAAGCT]GTTCCGAGCCTCCGG | 23607 |
rs781437065 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47590958 | ATTGGAAGAATCAAT[A/T]TTGTTAAAACTTCCA | 23607 |
rs781456166 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47483149 | GTTGTAGCATTTGAT[A/G]TCTGACTGCTATTCA | 23607 |
rs781460785 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47614459 | GAGTCAGAAGAAAGG[C/T]TGATCAGTGTAGCAG | 23607 |
rs781513806 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47556600 | GTGATCCACACGCCT[C/T]GGCCTCCCAAAGTGC | 23607 |
rs781541666 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47508609 | GGAGTGCAATAGCAC[C/G]ATTTTGGCTCACTGC | 23607 |
rs781544021 | in-del | -/T | 0.000266464 | 0.0115395 | intron-variant | CD2AP | GRCh38.p7 | 6:47533804 | CAAAATAGAAGGATA[-/T]TTTTATAACTGTGTC | 23607 |
rs781562635 | snp | A/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47489744 | AAGTCAGAGGTAAGA[A/T]GTGGAGGAGACAGAA | 23607 |
rs781632317 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47586705 | TTGGTAGAAGGAAAA[C/T]GATACTAGATTGGCA | 23607 |
rs781651664 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47568342 | AGGGATGTGAGAGCA[-/T]CCAAATGAAGATATT | 23607 |
rs781652294 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47504475 | ATGCAGATGCTCAGA[-/T]CTGTTATATAAAATG | 23607 |
rs781673980 | in-del | -/TGTGTGTGT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47491262 | TTTCTTCCTGATATG[-/TGTGTGTGT]ATGTGTGTGTGTGTG | 23607 |
rs781680398 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47517563 | CCAAAGTGCTGAGAT[G/T]GCAGGCCTAAGCCAC | 23607 |
rs781689187 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47549334 | GAAAGCTCCTAGAAC[G/T]GAGAAAAGAATTCAG | 23607 |
rs781689221 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47617735 | TAATTCTTATCTCAG[-/A]ATTAACCTTTCCTTC | 23607 |
rs781717540 | in-del | -/C | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47475810 | ATTCAATTGATAAAA[-/C]CTTTAATCTGAATTT | 23607 |
rs781732674 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47536037 | GAAGGAAAAATCATT[A/G]TGCAGTTGGTGCCAG | 23607 |
rs781755112 | snp | C/T | | | upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47476622 | TTGTGAGTTTGATCA[C/T]TCTTGTTATAAAATT | 23607 |
rs781780388 | snp | A/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47599052 | TATTTTTAATATTTT[A/C]TGTATACTAATATCT | 23607 |
rs781780992 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47571898 | ATGTGCAAATAACTT[-/A]ACCTGCTTGCCAGAA | 23607 |
rs796082455 | in-del | -/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47585750 | GAAATTTCCATAATG[-/G]AGAAATAACCATTGG | 23607 |
rs796101162 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47609522 | TCTTTGCAAAAAAAA[A/G]AAAAAAAAAGAAAAG | 23607 |
rs796108577 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47508548 | TCTTTTTTTTTTTGT[G/T]TTTTTTTTTTTTTTT | 23607 |
rs796159539 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47490808 | TAAGAGTGTATTGTA[C/T]TATGCAAACCTTTGT | 23607 |
rs796189533 | in-del | -/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47610969 | TATATATATATATAT[-/G]TATTTTTTTTTTTTT | 23607 |
rs796208648 | in-del | -/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47502452 | CGTTTTTGTAGAGAC[-/G]GGGTTTTGTTGTGTT | 23607 |
rs796229262 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47573580 | TGCAAGCTCCACCTC[C/T]CAGGTTCACGCCATT | 23607 |
rs796230087 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47511927 | ACTTTGGGAGGCCGA[A/G]GTGGGCGGATCACGA | 23607 |
rs796295425 | in-del | C/TT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47513156 | CCTTTTTTTTTTTTT[C/TT]TCTTCTTTTAAAGTA | 23607 |
rs796306397 | in-del | -/CCCCCC | | | intron-variant | CD2AP | GRCh38.p7 | 6:47529184 | TTAACTCTAGTACTG[-/CCCCCC]CCCCCCCCCCCAACT | 23607 |
rs796309674 | in-del | -/TTG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47508542 | TTCTTTCTTTTTTTT[-/TTG]TTTGTTTTTTTTTTT | 23607 |
rs796347283 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47543168 | AAAAAAAAAAAAAAA[A/G]AAAAGAAAAAGAAAA | 23607 |
rs796374240 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47613960 | TTAAACCACATGAAC[C/T]AGCCTCTGCTACCTT | 23607 |
rs796375827 | in-del | A/GTT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47619734 | TGCCAACATCTACTG[A/GTT]TTTGATTTTTTGATT | 23607 |
rs796379051 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47529945 | AGTGTTGTCTTCATT[C/T]CTCAGAAGCTCTGTG | 23607 |
rs796382195 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47609527 | GCAAAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAG | 23607 |
rs796452255 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47505921 | CCCCCACCTCCCTCC[C/T]GGACGGGGTGGCTGC | 23607 |
rs796462729 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47484365 | TCTTTTTTTTTTTTT[-/T]GTTATGTTTTGGTTT | 23607 |
rs796488171 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47488017 | GTTTCAAGATAATGG[A/G]TGAGATCCTTTTTTT | 23607 |
rs796505017 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47506778 | CATGAGAGGGAGACC[G/T]TGGGGAGAGGGAGAC | 23607 |
rs796524727 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47575840 | ATGAAGTATAAAGAG[-/T]TTTTTTTTTCTCCTC | 23607 |
rs796557196 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47543179 | AAAAAAAAAGAAAAA[A/G]AAAAAAGAAAAAAAA | 23607 |
rs796596542 | in-del | -/A | | | intron-variant | CD2AP | GRCh38.p7 | 6:47602729 | ACCGTGTCTCTACAG[-/A]AAAAAAAAAAAAAGC | 23607 |
rs796621681 | in-del | -/AC | | | intron-variant | CD2AP | GRCh38.p7 | 6:47589549 | TATGTACACATATAT[-/AC]ATACACACACACACA | 23607 |
rs796626610 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47609641 | GAAGTCAAGGCTGCA[A/G]TGAGCCGTGAACATG | 23607 |
rs796651064 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47493947 | TGCTTACCATATCCA[-/T]TTTTTTTCTTACATG | 23607 |
rs796662171 | in-del | -/AAA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47609514 | AAACCCCATCTTTGC[-/AAA]AAAAAAAAAAAAAAA | 23607 |
rs796664774 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47585945 | AAATTCCAGAATAAA[A/G]TTTGGTACAACTTAA | 23607 |
rs796676006 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47506674 | CGCGTGCCTGCAATC[C/G]CAGGCATTCGGCAGA | 23607 |
rs796676110 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47513157 | CCTTTTTTTTTTTTT[C/T]TTCTTCTTTTAAAGT | 23607 |
rs796688437 | in-del | -/TA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47547487 | AAAGTATCACAATTC[-/TA]TATATATATATGCAC | 23607 |
rs796689242 | in-del | -/TT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47536227 | GTTTATTAAACTTGA[-/TT]TTTTTTTTTTTGTTA | 23607 |
rs796692065 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47559712 | TTAGACTTTATTAAG[C/T]TCCTTGACACTTTTG | 23607 |
rs796748692 | in-del | -/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47556400 | CATTCTTTTTTTTTT[-/T]AATTTTGTTTTTTGA | 23607 |
rs796769791 | snp | A/G | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521651 | TAAAAAAGAAGAATA[A/G]ATTTGCATTCAGCAA | 23607 |
rs796829949 | in-del | -/TTTAA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47615779 | AATTTTAATTTTAAT[-/TTTAA]TTTAATTTAATTTAT | 23607 |
rs796830583 | in-del | -/C | | | intron-variant | CD2AP | GRCh38.p7 | 6:47500121 | CATTGCTCTGAGAAA[-/C]CAGCATTCATCCATA | 23607 |
rs796864568 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47482580 | AGATGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 23607 |
rs796870916 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47551711 | GGTATAGCCCAAATG[A/G]CTTGTGTGGGGCCCT | 23607 |
rs796879490 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47536650 | CATGGTAGCTCATTT[A/G]GTAAAACAAAGAAGT | 23607 |
rs796879563 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47506777 | GCATGAGAGGGAGAC[C/G]GTGGGGAGAGGGAGA | 23607 |
rs796888083 | in-del | -/AAAAAAAA | | | intron-variant | CD2AP | GRCh38.p7 | 6:47609514 | AAACCCCATCTTTGC[-/AAAAAAAA]AAAAAAAAAAGAAAA | 23607 |
rs796898532 | snp | A/G | | | intron-variant, upstream-variant-2KB | CD2AP | GRCh38.p7 | 6:47521964 | AGGTTGCAGTGAGCC[A/G]AGATCATGCCATTGC | 23607 |
rs796908802 | snp | C/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47606685 | TTTTAAAATTAACTT[C/G]AGCAGGTACATAATA | 23607 |
rs796939934 | in-del | -/TTTCT | | | intron-variant | CD2AP | GRCh38.p7 | 6:47508531 | CTCAAACTTTCTTTC[-/TTTCT]TTTTTTTTTTGTTTT | 23607 |
rs796968940 | snp | A/G | | | intron-variant | CD2AP | GRCh38.p7 | 6:47609536 | AAAAAAAAAAAGAAA[A/G]GAAAAGAAAAGAAAA | 23607 |
rs796978855 | snp | G/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47503508 | AAATGTTAAGAAATA[G/T]ATATACTTTTAAAAT | 23607 |
rs796990870 | in-del | -/TG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47610986 | ATTTTTTTTTTTTTT[-/TG]AATATAAAACATTTT | 23607 |
rs797004904 | in-del | -/T | | | utr-variant-3-prime | CD2AP | GRCh38.p7 | 6:47624594 | TTACAAGTAATCTGT[-/T]AAGATATACTATTTG | 23607 |
rs797007470 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47505614 | GGGCGGCTGGCCGGG[C/T]GGGGGGGGCTGACCC | 23607 |
rs797007825 | multinucleotide-polymorphism | GT/TG | | | intron-variant | CD2AP | GRCh38.p7 | 6:47508545 | TTTCTTTTTTTTTTT[GT/TG]TTTTTTTTTTTTTTT | 23607 |
rs797011534 | snp | C/T | | | intron-variant | CD2AP | GRCh38.p7 | 6:47566690 | TCATTGTTCAACTCC[C/T]ACTAATGAGTGAGAA | 23607 |
rs864622037 | snp | C/T | | | missense | CD2AP | GRCh38.p7 | 6:47574082 | CTGTTTTGGCTGGGC[C/T]TACTTCACCTATACC | 23607 |