SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs12533063 | snp | C/T | 0.29046 | 0.246704 | intron-variant | CADPS2 | GRCh38.p7 | 7:122632488 | atttgctcatgtttt[C/T]tggccacttgtacat | 93664 |
rs12533238 | snp | C/G | 0.476227 | 0.106402 | intron-variant | CADPS2 | GRCh38.p7 | 7:122788014 | CAATAAACATCCCCC[C/G]TGTGAGAATAAGAGC | 93664 |
rs12533577 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | CADPS2 | GRCh38.p7 | 7:122337720 | ACCAGACAGCGGTAA[C/T]TCGAGAGCAGAGGTT | 93664 |
rs12533664 | snp | C/G | 0.104859 | 0.203554 | intron-variant | CADPS2 | GRCh38.p7 | 7:122412185 | ACTTTAAATTTGAAC[C/G]CATCCTAAAAAAAGA | 93664 |
rs12533750 | snp | C/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122753338 | TCACCCTACAGTTTT[C/T]TAAATACATGCAAAG | 93664 |
rs12533870 | snp | C/T | 0.210446 | 0.246851 | intron-variant | CADPS2 | GRCh38.p7 | 7:122723728 | aaagacacatgcaca[C/T]atatgtttattgtgg | 93664 |
rs12534868 | snp | G/T | 0.323908 | 0.238825 | intron-variant | CADPS2 | GRCh38.p7 | 7:122749910 | TTATACATACAGAAT[G/T]CTGCTAATAAGAAAA | 93664 |
rs12535299 | snp | A/G | 0.485596 | 0.0836329 | intron-variant | CADPS2 | GRCh38.p7 | 7:122607753 | ATTTGGCTAATGCTT[A/G]TCTCTTTAGGCTTCA | 93664 |
rs12535500 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122750517 | TGCCTTTGTCTCTTA[A/G]GACTTAATAATGTCT | 93664 |
rs12535792 | snp | A/G | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122583718 | CATATCATATACCTC[A/G]CAATAGCATATATAA | 93664 |
rs12536063 | snp | A/C | 0.282895 | 0.247826 | intron-variant | CADPS2 | GRCh38.p7 | 7:122362432 | TAGGGTGAGGGGGGT[A/C]GGATGTGGAATTCAA | 93664 |
rs12536083 | snp | A/C | 0.283421 | 0.247756 | intron-variant | CADPS2 | GRCh38.p7 | 7:122362502 | TTTCTATGAAATAAA[A/C]AAACACATACACTAT | 93664 |
rs12536618 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | CADPS2 | GRCh38.p7 | 7:122351201 | gtgttactaaacatc[A/G]tctctactaaaaata | 93664 |
rs12537200 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122645477 | tgtgtatatatgtat[A/G]tatatttagcgtata | 93664 |
rs12537488 | snp | C/G | 0.217851 | 0.247924 | intron-variant | CADPS2 | GRCh38.p7 | 7:122728563 | GACCTGAAGATTTGT[C/G]CTGAAAGTAAAGTAT | 93664 |
rs12537637 | snp | A/T | 0.444444 | 0.157135 | intron-variant | CADPS2 | GRCh38.p7 | 7:122625056 | TGATGATTAATTATT[A/T]TTTTTTTTTTTGAGA | 93664 |
rs12537918 | snp | A/C | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122771603 | ATAAATGTAAAGGAT[A/C]CAATGGGAGTAGAAA | 93664 |
rs12538206 | snp | C/T | 0.406468 | 0.194981 | intron-variant | CADPS2 | GRCh38.p7 | 7:122363663 | AAAGGACAGCTATCC[C/T]GCCCACCTTACAAGA | 93664 |
rs12538235 | snp | C/T | 0.346368 | 0.23068 | intron-variant | CADPS2 | GRCh38.p7 | 7:122750573 | TTAATCTTTTCAGTG[C/T]TGTCTGAAAAAGCAG | 93664 |
rs12538303 | snp | C/G | 0.282895 | 0.247826 | intron-variant | CADPS2 | GRCh38.p7 | 7:122364060 | ATGCTCTTTACCCAT[C/G]ATGCTACAGAACTGT | 93664 |
rs12538550 | snp | A/G | 0.200801 | 0.245111 | intron-variant | CADPS2 | GRCh38.p7 | 7:122687687 | CCTCCCTCTATTCCT[A/G]TCACACTTGCCAGCT | 93664 |
rs12538608 | snp | C/G | 0.0498117 | 0.149749 | intron-variant | CADPS2 | GRCh38.p7 | 7:122359209 | GGAGGCATGAAAATT[C/G]TCATTAAATATGCAA | 93664 |
rs12538802 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122550826 | TGAATCATTTAACCA[C/T]TCAAAACATAGCTGG | 93664 |
rs12538945 | snp | A/C | 0.199254 | 0.244796 | intron-variant | CADPS2 | GRCh38.p7 | 7:122642566 | TTTTTTTTTTTTTTT[A/C]CAACTTATTATATTG | 93664 |
rs12539965 | snp | A/G | 0.487871 | 0.076925 | intron-variant | CADPS2 | GRCh38.p7 | 7:122594348 | CAGAAAAATATTGGG[A/G]AATGGGTTGGGGTGG | 93664 |
rs12540444 | snp | C/T | 0.0700422 | 0.173537 | intron-variant | CADPS2 | GRCh38.p7 | 7:122336507 | AAGTCACAGGCTCTA[C/T]ATATAGAGGTCAGAA | 93664 |
rs12540674 | snp | A/T | 0.35809 | 0.225425 | intron-variant | CADPS2 | GRCh38.p7 | 7:122750358 | ATATATACTAAAAAG[A/T]ATCCATTATTTAACT | 93664 |
rs12540906 | snp | G/T | 0 | 0 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122559157 | ATAGAGGAATTACAG[G/T]TTCACTTGGAAGTCT | 93664 |
rs12666284 | snp | C/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122443317 | AGAAGCTTAATTAAT[C/T]TTTACAAAACAAGTT | 93664 |
rs12666307 | snp | C/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122443394 | TGGGTTTTTACCACT[C/T]TGGCAGCTCTATAAC | 93664 |
rs12667210 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122592850 | cagggggatgggggg[A/G]ggggggaggaatagc | 93664 |
rs12667779 | snp | A/G | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122403403 | AATCTGCAAATCACC[A/G]TAAAATAAAAGCCAA | 93664 |
rs12667803 | snp | A/T | 0.440884 | 0.161442 | intron-variant | CADPS2 | GRCh38.p7 | 7:122353017 | CAACAGTGCTTTACA[A/T]TTCAAAGCACATTCA | 93664 |
rs12668535 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122371333 | ttatagttctgcatt[A/G]ctggggaggccttag | 93664 |
rs12668539 | snp | C/T | 0.494315 | 0.0530107 | intron-variant | CADPS2 | GRCh38.p7 | 7:122513916 | CAAATGTTTTAACTA[C/T]AAAATTCTGATAGTA | 93664 |
rs12668581 | snp | C/T | 0.387263 | 0.208947 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122544248 | GTGCAGGAAAGATTA[C/T]ATATATGCACAAATA | 93664 |
rs12668852 | snp | C/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122447497 | caattaaccatcact[C/T]tagggacacctttct | 93664 |
rs12668965 | snp | C/T | 0.27893 | 0.24832 | intron-variant | CADPS2 | GRCh38.p7 | 7:122688696 | AGCAGGGCAATGATA[C/T]CTTTTACAAACAATA | 93664 |
rs12669155 | snp | C/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122443205 | CCCACTGGGTATGTT[C/T]TAAATTAGCATTAGC | 93664 |
rs12669923 | snp | A/T | 0.323197 | 0.239044 | intron-variant | CADPS2 | GRCh38.p7 | 7:122732830 | ATGTATATTATATAT[A/T]ATATACATTATATAT | 93664 |
rs12670456 | snp | A/G | 0.39709 | 0.20215 | intron-variant | CADPS2 | GRCh38.p7 | 7:122462727 | AATCACCTACATATC[A/G]TGCAAAAATCATTAT | 93664 |
rs12670651 | snp | A/T | 0.392325 | 0.205532 | intron-variant | CADPS2 | GRCh38.p7 | 7:122443461 | AAATTCAGCCACATT[A/T]TATACCTAACATGAA | 93664 |
rs12670792 | snp | C/G | 0.157642 | 0.232314 | intron-variant | CADPS2 | GRCh38.p7 | 7:122626956 | GTCTCTTGAAACAGA[C/G]ATTTTGCCCTGTAGT | 93664 |
rs12671364 | snp | C/T | 0.382666 | 0.211895 | intron-variant | CADPS2 | GRCh38.p7 | 7:122347816 | AAAGATTACTACTAT[C/T]AATACTTGAAGGAAA | 93664 |
rs12671420 | snp | A/G | 0.397452 | 0.201886 | intron-variant | CADPS2 | GRCh38.p7 | 7:122452190 | AATAACAGAAATTTA[A/G]AATTTATTCTGTATC | 93664 |
rs12671596 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122592849 | ccagggggatggggg[A/G]aggggggaggaatag | 93664 |
rs12673310 | snp | G/T | 0.437118 | 0.165792 | intron-variant | CADPS2 | GRCh38.p7 | 7:122405414 | ACATGTGTAATCCCA[G/T]CACTTTGGGAGGCTG | 93664 |
rs12674064 | snp | A/T | 0.470327 | 0.118136 | intron-variant | CADPS2 | GRCh38.p7 | 7:122392401 | ACAGTTTTTTTTTTT[A/T]AAATCATCACAAAAA | 93664 |
rs12674113 | snp | A/C | 0.342134 | 0.232404 | intron-variant | CADPS2 | GRCh38.p7 | 7:122732729 | TTATATATTACATAT[A/C]ATTATATATTATATA | 93664 |
rs12674193 | snp | A/C | 0.401037 | 0.199218 | intron-variant | CADPS2 | GRCh38.p7 | 7:122873987 | gtgtctgttcatatc[A/C]ttcacccactttttg | 93664 |
rs12706405 | snp | A/C | 0.326976 | 0.237854 | utr-variant-3-prime | CADPS2 | GRCh38.p7 | 7:122319692 | ACAAAACGAACCTGG[A/C]ACATAAATTATAATT | 93664 |
rs12706408 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | CADPS2 | GRCh38.p7 | 7:122340788 | TTTTTATATTGGGAT[C/T]AGGTTGAAGATGGTT | 93664 |
rs12706409 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | CADPS2 | GRCh38.p7 | 7:122417679 | TTCTAATTTTGTCAG[G/T]AAGAGAAGGCACCTA | 93664 |
rs12706410 | snp | G/T | 0.0448719 | 0.142907 | intron-variant | CADPS2 | GRCh38.p7 | 7:122418416 | CTAAGAATGATGGGT[G/T]ATTATGGGAGACTTT | 93664 |
rs12706411 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | CADPS2 | GRCh38.p7 | 7:122425165 | aagtttctttttata[C/T]agacggggtctcact | 93664 |
rs12706412 | snp | A/C | 0.0952156 | 0.196321 | intron-variant | CADPS2 | GRCh38.p7 | 7:122430360 | ATAATTTTCAGGAAA[A/C]AGTAGGAACTGTTAT | 93664 |
rs12706413 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | CADPS2 | GRCh38.p7 | 7:122435274 | gaaagggttcatatc[C/T]aaactatttaagtaa | 93664 |
rs12706415 | snp | A/G | 0.077417 | 0.180873 | intron-variant | CADPS2 | GRCh38.p7 | 7:122456917 | TCAATCTGGCAGATT[A/G]CTGCATTCTAAAACA | 93664 |
rs12706416 | snp | A/T | 0.119978 | 0.213528 | intron-variant | CADPS2 | GRCh38.p7 | 7:122460718 | aattataaaagatct[A/T]aggaaacaaaaaatg | 93664 |
rs12706419 | snp | C/T | 0.167809 | 0.236103 | intron-variant, upstream-variant-2KB | CADPS2, LOC105375481 | GRCh38.p7 | 7:122529480 | AAGACTAGAAATCTG[C/T]TACATGAACTTGTAG | 93664 |
rs12706420 | snp | C/T | 0.266819 | 0.249434 | intron-variant | CADPS2 | GRCh38.p7 | 7:122570596 | catgtatgtttattg[C/T]ggcactattcacaat | 93664 |
rs12706421 | snp | A/T | 0.163892 | 0.234703 | intron-variant | CADPS2 | GRCh38.p7 | 7:122587588 | catatgcatgcatgt[A/T]tctttgcaacagaat | 93664 |
rs12706422 | snp | C/G | 0.118584 | 0.212673 | intron-variant | CADPS2 | GRCh38.p7 | 7:122608100 | tgcatgtctgtagtc[C/G]cagctactcaagagg | 93664 |
rs12706423 | snp | C/T | 0.247621 | 0.249989 | intron-variant | CADPS2 | GRCh38.p7 | 7:122609411 | TAGAAACAATTCCTC[C/T]GTATCTCATTCATAC | 93664 |
rs12706424 | snp | A/G | 0.248188 | 0.249993 | intron-variant | CADPS2 | GRCh38.p7 | 7:122613020 | aagctggactcttac[A/G]ttacaccatatacaa | 93664 |
rs12706425 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | CADPS2 | GRCh38.p7 | 7:122613277 | gcaaatcacatatat[A/G]atgtgggcctagtat | 93664 |
rs12706426 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | CADPS2 | GRCh38.p7 | 7:122631625 | CACATTTGTCTGAAA[A/G]AAAAGTAAGCAACAA | 93664 |
rs12706427 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | CADPS2 | GRCh38.p7 | 7:122648666 | TCCTGCCAGAAATTC[C/T]GACACTTTTATCTTG | 93664 |
rs12706434 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | CADPS2 | GRCh38.p7 | 7:122666528 | tttatatttttagta[A/G]agacagggtttcacc | 93664 |
rs12706436 | snp | C/T | 0.318896 | 0.240319 | intron-variant | CADPS2 | GRCh38.p7 | 7:122732392 | GACCTACAATCAAGA[C/T]GGAAAAGGCTATTCA | 93664 |
rs12706437 | snp | A/G | 0.319376 | 0.240181 | intron-variant | CADPS2 | GRCh38.p7 | 7:122737507 | TGAGCCACTGCACCC[A/G]GACACTAATGGTTAG | 93664 |
rs12706438 | snp | C/T | 0.337386 | 0.23423 | intron-variant | CADPS2 | GRCh38.p7 | 7:122740670 | aTACTGAAATGTCAT[C/T]AATTTATTTGCATTA | 93664 |
rs12706439 | snp | A/T | 0.356169 | 0.226336 | intron-variant | CADPS2 | GRCh38.p7 | 7:122741145 | GTGGTATACTATTCA[A/T]TGCATTAAAAGAATG | 93664 |
rs12706440 | snp | A/G | 0.34146 | 0.23267 | intron-variant | CADPS2 | GRCh38.p7 | 7:122741519 | CACGGAGACTGGACA[A/G]CACACCAATTTTTTC | 93664 |
rs12706441 | snp | C/T | 0.364609 | 0.222182 | intron-variant | CADPS2 | GRCh38.p7 | 7:122742891 | TTTTAAAAATATTCA[C/T]CAGTTCAGGATTAAG | 93664 |
rs12706442 | snp | C/T | 0.339203 | 0.233544 | intron-variant | CADPS2 | GRCh38.p7 | 7:122761527 | ATGAAAAGTCTCTAA[C/T]ACAAAATCTTTAAAA | 93664 |
rs12706443 | snp | C/T | 0.339203 | 0.233544 | intron-variant | CADPS2 | GRCh38.p7 | 7:122761634 | CTGAAAAATAAAATA[C/T]ACAACAGGAAACAAG | 93664 |
rs12706444 | snp | A/G | 0.356169 | 0.226336 | intron-variant | CADPS2 | GRCh38.p7 | 7:122763072 | GATCAACTTTGTGGA[A/G]GGCTGTGTTAACAGG | 93664 |
rs12706445 | snp | C/T | 0.331642 | 0.236293 | intron-variant | CADPS2 | GRCh38.p7 | 7:122775697 | CTCCCCCTAATAAAA[C/T]ATGACCATAAGCATG | 93664 |
rs12706446 | snp | A/T | 0.330947 | 0.236533 | intron-variant | CADPS2 | GRCh38.p7 | 7:122778283 | agagatgatttaggg[A/T]atctggtggaagaaa | 93664 |
rs12706447 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122784292 | GGTCGTTGGGTACTG[G/T]TTACTTTTAGATTTT | 93664 |
rs12706448 | snp | G/T | 0.392511 | 0.205404 | intron-variant | CADPS2 | GRCh38.p7 | 7:122784551 | ATCTCTCAAGTCCTT[G/T]TCTTAATCTAGGCAG | 93664 |
rs12706451 | snp | A/G | 0.348574 | 0.229746 | intron-variant | CADPS2 | GRCh38.p7 | 7:122807040 | TTAGGGGATACTGTA[A/G]GGACAGAGCAAGAGG | 93664 |
rs12706452 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | CADPS2 | GRCh38.p7 | 7:122813129 | GTACGGAAAAAAAAG[C/T]TTTTAAAAAGTTGGT | 93664 |
rs12706453 | snp | C/T | 0.308661 | 0.24302 | intron-variant | CADPS2 | GRCh38.p7 | 7:122829439 | ACAAGGAGAAATGAG[C/T]CTTATATATAGGTAA | 93664 |
rs12706454 | snp | A/G | 0.323434 | 0.238972 | intron-variant | CADPS2 | GRCh38.p7 | 7:122870987 | TGCTTTTCAGAAATT[A/G]TTTTATGTATCTTCC | 93664 |
rs13221089 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122516317 | aggcaggaggattgc[C/T]tgagaacaggagttc | 93664 |
rs13221540 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | CADPS2 | GRCh38.p7 | 7:122664747 | CCTCCATAAATTATA[C/T]GCTGTTATTGAGCTT | 93664 |
rs13221717 | snp | C/T | 0.312348 | 0.242101 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817662 | gggcaagtaccccaa[C/T]cccttctctccttgt | 93664 |
rs13222194 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122885098 | CAGGTTCAGCATTCT[A/T]TTAAAAAGATTTCCT | 93664 |
rs13222202 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122885137 | TATTGTAAACATTTA[A/T]CCACTTAGGACAATT | 93664 |
rs13222207 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122885155 | ACTTAGGACAATTTG[A/T]GTCATTACTCGTGTC | 93664 |
rs13222266 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | CADPS2 | GRCh38.p7 | 7:122659436 | aaaaacttcccaaac[C/T]gaaatacaaagagaa | 93664 |
rs13222290 | snp | A/G | 0.400325 | 0.199756 | intron-variant | CADPS2 | GRCh38.p7 | 7:122580840 | TTGAACCCAGGGACA[A/G]AAATATGTTACATGA | 93664 |
rs13222302 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122885207 | TGGGGTCTTGTTTTG[A/C]AACTCAAGTTGGCCA | 93664 |
rs13222449 | snp | A/G | 0.400325 | 0.199756 | intron-variant | CADPS2 | GRCh38.p7 | 7:122580727 | CTTTTCATGGGGAAA[A/G]TGGAAAAGATAAGAG | 93664 |
rs13222569 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122885195 | ACATCAGGCCCCTGG[A/G]GTCTTGTTTTGAAAC | 93664 |
rs13222975 | snp | C/G | 0.079617 | 0.182947 | intron-variant | CADPS2 | GRCh38.p7 | 7:122490920 | ATATGAAGGGAGAGA[C/G]AGAAGTACAAGCATG | 93664 |
rs13223497 | snp | A/C | 0.0584853 | 0.160693 | intron-variant | CADPS2 | GRCh38.p7 | 7:122721516 | tctctgaatagacca[A/C]taacaggctctgaaa | 93664 |
rs13224091 | snp | A/G | 0.308166 | 0.243139 | intron-variant | CADPS2 | GRCh38.p7 | 7:122839704 | ccactggtcatcaga[A/G]aaatgcaaatcaaaa | 93664 |
rs13224166 | snp | A/C | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122626975 | TTGCCCTGTAGTTTC[A/C]CTGTTATTATATTGT | 93664 |
rs13224171 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | CADPS2 | GRCh38.p7 | 7:122721993 | acaaaattcaacaac[C/T]cttcatgctaaaaac | 93664 |
rs13224552 | snp | A/C | 0.339203 | 0.233544 | intron-variant | CADPS2 | GRCh38.p7 | 7:122769409 | ACTGAGCCCTCCAGG[A/C]ACAGAATCCCTACAT | 93664 |
rs13225231 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122399657 | TCTCTCAAGGGTGGG[G/T]TTCTTTTTTTTTTTT | 93664 |
rs13225523 | snp | A/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122496996 | GAAATAATCTCATAT[A/T]TATACCTGGGATTGT | 93664 |
rs13225807 | snp | G/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122497034 | TTCTCGGACTGTTCT[G/T]TCTTTCTGGTAACTT | 93664 |
rs13226270 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | CADPS2 | GRCh38.p7 | 7:122660641 | ttgggccaagcgctg[C/T]ggctcacacctgtaa | 93664 |
rs13226382 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | CADPS2 | GRCh38.p7 | 7:122660752 | catctctactaaaaa[C/T]acaaaaattagccag | 93664 |
rs13226441 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | CADPS2 | GRCh38.p7 | 7:122748607 | ATGACATAAAATTAC[C/T]TTCCTCAGAAATGTC | 93664 |
rs13226509 | snp | C/T | 0.181022 | 0.240296 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122542882 | ACATCCATAAACACA[C/T]ACAGTTCTCACAACC | 93664 |
rs13226818 | snp | A/G | 0.311614 | 0.242289 | intron-variant | CADPS2 | GRCh38.p7 | 7:122815921 | TTGTACATATTTAGG[A/G]GTACATGTGAAATTT | 93664 |
rs13227070 | snp | A/T | 0.306679 | 0.24349 | intron-variant | CADPS2 | GRCh38.p7 | 7:122816105 | ATCATGCTACTGAAC[A/T]TTAGATCTTATCCTT | 93664 |
rs13227173 | snp | A/C | 0.310632 | 0.242536 | intron-variant | CADPS2 | GRCh38.p7 | 7:122816099 | CACCTTATCATGCTA[A/C]TGAACATTAGATCTT | 93664 |
rs13227288 | snp | A/G | 0.311369 | 0.242351 | intron-variant | CADPS2 | GRCh38.p7 | 7:122816052 | TGTTTTAGTTATGTT[A/G]AAATATACAATAAAT | 93664 |
rs13227529 | snp | A/C | 0.308908 | 0.242961 | intron-variant | CADPS2 | GRCh38.p7 | 7:122775590 | TTCACCCTCTGTGCC[A/C]TATTTCTTTTGTACT | 93664 |
rs13227854 | snp | C/G | 0.181978 | 0.240568 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539928 | TAATGTGTCCTTAAT[C/G]TTCATAAAACTTCAA | 93664 |
rs13228393 | snp | A/G | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122740304 | gtagcttttttcata[A/G]ttgcaaaattcagta | 93664 |
rs13228884 | snp | A/G | 0.303187 | 0.244277 | intron-variant | CADPS2 | GRCh38.p7 | 7:122645367 | TGTATACATGTACAT[A/G]TATACACACATATGT | 93664 |
rs13229359 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122762029 | atatatatatatata[C/T]acacacacacacaca | 93664 |
rs13229788 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | CADPS2 | GRCh38.p7 | 7:122637161 | cttctgactgcatta[C/T]gaaattttgcttttt | 93664 |
rs13229793 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122637172 | attatgaaattttgc[C/T]ttttttttttttttt | 93664 |
rs13230792 | snp | G/T | 0.0681886 | 0.171594 | intron-variant | CADPS2 | GRCh38.p7 | 7:122662162 | GATTAAAAACAAACA[G/T]GTATATTATAGAAGT | 93664 |
rs13231250 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | CADPS2 | GRCh38.p7 | 7:122475569 | AATTATAGAGTCAGA[C/T]TCATAATAAAACTCA | 93664 |
rs13231659 | snp | A/T | 0.324382 | 0.238678 | intron-variant | CADPS2 | GRCh38.p7 | 7:122862732 | CCATTTTGTTTTTTT[A/T]AAAAAAAAAAGAATA | 93664 |
rs13231771 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122540977 | TGAACACTATAAATA[C/T]ATAGAGAGTACTTAA | 93664 |
rs13231815 | snp | A/C | 0.0391387 | 0.134304 | intron-variant | CADPS2 | GRCh38.p7 | 7:122358142 | aacattttgctgttg[A/C]cagtttgtttttgga | 93664 |
rs13232111 | snp | A/G | 0.317451 | 0.240729 | intron-variant | CADPS2 | GRCh38.p7 | 7:122746913 | GAATTGGCAAGTCTT[A/G]TTGGTCATTATCTTC | 93664 |
rs13232404 | snp | A/C | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122345472 | AGAAGATACAGGATC[A/C]CAAAAAGGAGACTAT | 93664 |
rs13232552 | snp | A/C | 0.00472811 | 0.0483911 | intron-variant | CADPS2 | GRCh38.p7 | 7:122734291 | GATTTTGAAGTGCCC[A/C]CAGTACCTGACATAG | 93664 |
rs13233113 | snp | C/T | 0.365232 | 0.22186 | intron-variant | CADPS2 | GRCh38.p7 | 7:122741929 | TTCTCTTTTCTAGAA[C/T]AAATTTTACCAGTTC | 93664 |
rs13233385 | snp | C/T | 0.331179 | 0.236453 | intron-variant | CADPS2 | GRCh38.p7 | 7:122783527 | cccttgacctggtga[C/T]ggatgaataatgtac | 93664 |
rs13233633 | snp | A/G | 0.317933 | 0.240593 | intron-variant | CADPS2 | GRCh38.p7 | 7:122742189 | TGAGGTCAGGAGTTC[A/G]AGACCAGCGTGGCCA | 93664 |
rs13233848 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122516316 | aaggcaggaggattg[C/T]ttgagaacaggagtt | 93664 |
rs13234082 | snp | A/C | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122516611 | AATAAACACTCAAAA[A/C]CAATCtaaaaatcaa | 93664 |
rs13234402 | snp | G/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122324749 | TTTTCTGCCATAAGG[G/T]GAAATTTCTGTCCCA | 93664 |
rs13235533 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122564853 | cacacacatgcacac[A/G]cacacacacacacac | 93664 |
rs13235728 | snp | C/T | 0.305436 | 0.243776 | intron-variant | CADPS2 | GRCh38.p7 | 7:122768758 | TAAGCAAATATTTTC[C/T]CTTTTATGTCTTGTA | 93664 |
rs13235975 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122835879 | tatccgggagaactt[A/C]cccaatctagcaagg | 93664 |
rs13236195 | snp | A/G | 0.0770498 | 0.180522 | intron-variant | CADPS2 | GRCh38.p7 | 7:122835869 | tgaaggatattatcc[A/G]ggagaacttccccaa | 93664 |
rs13236261 | snp | C/T | 0.317933 | 0.240593 | intron-variant | CADPS2 | GRCh38.p7 | 7:122742311 | gaggcaggagaatcg[C/T]ttgaacccgagaggc | 93664 |
rs13236662 | snp | C/T | 0.391954 | 0.205789 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122559735 | GAGACTGTGCCATTG[C/T]ACTCCAGCCTGGGTG | 93664 |
rs13236730 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122885060 | AAACTGAGGGAACTG[G/T]TACCGATTTCTACAG | 93664 |
rs13237014 | snp | A/T | 0.192088 | 0.2432 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122560059 | GTGACTGGAGACCTG[A/T]GCAGGAAAAAGTTTA | 93664 |
rs13237142 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | CADPS2 | GRCh38.p7 | 7:122713007 | ggttacggcaCACAC[A/G]AAAATAAATCCTGTC | 93664 |
rs13238065 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122399660 | CTCAAGGGTGGGTTT[C/T]TTTTTTTTTTTTTTt | 93664 |
rs13238360 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | CADPS2 | GRCh38.p7 | 7:122481140 | CTCATTCTGATGAGG[C/T]AGAACATTTTCTTTC | 93664 |
rs13239090 | snp | A/C/G | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122778639 | ccagctgctccagcc[A/C/G]cagctaaaggaccaa | 93664 |
rs13239116 | snp | C/T | 0.077417 | 0.180873 | intron-variant | CADPS2 | GRCh38.p7 | 7:122447622 | gcagtcaggcgatct[C/T]ggctcactgcagcct | 93664 |
rs13239193 | snp | A/G | 0.296619 | 0.245615 | intron-variant | CADPS2 | GRCh38.p7 | 7:122778687 | ggcctcacggggtgc[A/G]agccccaagccttgg | 93664 |
rs13239245 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122447733 | taattttgtattttt[C/T]gtagaaacagggttt | 93664 |
rs13239280 | snp | C/G | 0.331411 | 0.236373 | intron-variant | CADPS2 | GRCh38.p7 | 7:122778679 | tgggttgtggcctca[C/G]ggggtgcaagcccca | 93664 |
rs13239569 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | CADPS2 | GRCh38.p7 | 7:122661123 | gaatactacatcacg[A/G]taaaggagtcaattc | 93664 |
rs13239616 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122630824 | ATATGTTTCCAAGTT[A/G/T]ATTTTTAAAAAACCA | 93664 |
rs13240014 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122497039 | GGACTGTTCTGTCTT[A/T]CTGGTAACTTGTTCT | 93664 |
rs13240083 | snp | G/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122497063 | TTGTTCTATTTGTAT[G/T]TATGCAGTGAGTATT | 93664 |
rs13240237 | snp | C/T | 0.32885 | 0.23724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122852286 | GTACCTGAATTCAAC[C/T]GTTCATTCAACTACA | 93664 |
rs13241158 | snp | G/T | 0.325327 | 0.238382 | downstream-variant-500B | CADPS2 | GRCh38.p7 | 7:122318141 | TCCTGGGTGTAGAAG[G/T]GAAGTAGCAGAGAAC | 93664 |
rs13241783 | snp | A/G | 0.0763149 | 0.179815 | intron-variant | CADPS2 | GRCh38.p7 | 7:122453706 | TTTCTATTTTGTTCA[A/G]CTGTCAAATGAGATT | 93664 |
rs13242616 | snp | C/T | 0.487432 | 0.0782705 | intron-variant | CADPS2 | GRCh38.p7 | 7:122381464 | TGTTTTTCTCTGTTT[C/T]CATAACTTCCATTTT | 93664 |
rs13244476 | snp | A/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122552790 | Gtttttttttttttt[A/T]tttattattGTGCCA | 93664 |
rs13244705 | snp | A/C | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122883484 | TACAGAATAAAATAA[A/C]CAACGGATTAGTGAT | 93664 |
rs13244708 | snp | A/C | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122883487 | AGAATAAAATAAACA[A/C]CGGATTAGTGATTTT | 93664 |
rs13245159 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122816943 | tttcctggctcatcc[C/T]ggctcaaaaagcacc | 93664 |
rs13245302 | snp | A/G | 0.312491 | 0.242064 | intron-variant | CADPS2 | GRCh38.p7 | 7:122850362 | GTCAGATCACCACCT[A/G]GGGGGGTGACACCTT | 93664 |
rs13245411 | snp | C/G | 0.298144 | 0.245321 | intron-variant | CADPS2 | GRCh38.p7 | 7:122826126 | gcctagtggagagta[C/G]cgactttcatcatca | 93664 |
rs13246063 | snp | A/C | 0.192401 | 0.243274 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122550087 | GTTTATGTAGGCATG[A/C]TGTCCCAACCTCTGG | 93664 |
rs13246664 | snp | A/G | 0.314057 | 0.241654 | intron-variant | CADPS2 | GRCh38.p7 | 7:122821240 | tgatttattgatggc[A/G]gttccaccaggccta | 93664 |
rs13246934 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122537700 | GAAATAGAAGAAAGG[A/G]AATAATGAAGATTTG | 93664 |
rs13247049 | snp | A/G | 0.482008 | 0.0931261 | intron-variant | CADPS2 | GRCh38.p7 | 7:122419587 | TGGGGGAGAAAGACC[A/G]TATCTTTCATCAGAT | 93664 |
rs13247461 | snp | C/T | 0.455502 | 0.142369 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122538048 | TATTCAAAAATACCT[C/T]CCCTTACCTCCAACC | 93664 |
rs13247691 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122744106 | ACCAGATGCAAGCAA[A/G]TGTATGCCTGACTTC | 93664 |
rs13247906 | snp | A/G | 0.0898077 | 0.191933 | intron-variant | CADPS2 | GRCh38.p7 | 7:122691078 | tactcagcatactcc[A/G]ctgctctaagcaggt | 93664 |
rs13307838 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122705468 | ttatctatattatat[A/T]Ttatatatatttata | 93664 |
rs13307854 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122705544 | ttatctatattatat[A/T]ttatatatatttata | 93664 |
rs13308188 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122705447 | tatgtaatataatat[A/T]atatattatCTATAT | 93664 |
rs13308228 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122705469 | tatctatattatata[A/T]tatatatatttatat | 93664 |
rs13308244 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122705545 | tatctatattatata[A/T]tatatatatttatat | 93664 |
rs13308292 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | CADPS2 | GRCh38.p7 | 7:122705591 | ttatatattatataa[A/T]atattttatatatta | 93664 |
rs13308298 | snp | C/T | 0.300673 | 0.244811 | intron-variant | CADPS2 | GRCh38.p7 | 7:122705618 | attatataacattta[C/T]atatattatatatga | 93664 |
rs13309209 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122822694 | cattccaccacaaaa[A/G]aagtgtaaatggccg | 93664 |
rs13311063 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | CADPS2 | GRCh38.p7 | 7:122816901 | cgatccttgccttaa[A/G]tgatggcattacctt | 93664 |
rs13311160 | snp | A/C/G | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817060 | aaaacggccccaccc[A/C/G]tatctcccttcgcta | 93664 |
rs13311162 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122817075 | atatctcccttcgct[A/G]actctcttttcagac | 93664 |
rs13311167 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817087 | gctaactctcttttc[A/G]gactcagcccgcctg | 93664 |
rs13311168 | snp | C/T | 0.031825 | 0.122064 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817049 | tcaaatcctataaaa[C/T]ggccccacccatatc | 93664 |
rs13311198 | snp | A/C/G | 0.0337553 | 0.125452 | intron-variant | CADPS2 | GRCh38.p7 | 7:122816907 | ttgccttaaatgatg[A/C/G]cattaccttgtgaaa | 93664 |
rs13311222 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122817162 | ttggtggtctcttca[A/C]acggacgcacatgaA | 93664 |
rs13311224 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122817171 | tcttcaaacggacgc[A/G]catgaAAtttggtgc | 93664 |
rs13311291 | snp | A/C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122817094 | ctcttttcagactca[A/C/G]cccgcctgcacccag | 93664 |
rs13311293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817119 | acccaggtgaaataa[A/G]cagccatgttgctca | 93664 |
rs13311506 | snp | C/T | 0.031825 | 0.122064 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817034 | ttttcctttacctac[C/T]caaatcctataaaac | 93664 |
rs13362819 | snp | A/G | 0.421209 | 0.182174 | intron-variant | CADPS2 | GRCh38.p7 | 7:122480476 | AAAACATATCCACTG[A/G]ATATTTTAGATGTAA | 93664 |
rs13438501 | snp | C/T | 0.0289187 | 0.116718 | intron-variant | CADPS2 | GRCh38.p7 | 7:122379319 | TTAAAAAATTCTCCA[C/T]TGACAATTTTTCACT | 93664 |
rs16870811 | snp | C/T | 0.190205 | 0.242744 | intron-variant | CADPS2 | GRCh38.p7 | 7:122363970 | AAACCACTGGGATTC[C/T]GCCTGTTTCAAGGTT | 93664 |
rs16870873 | snp | C/G | 0.311614 | 0.242289 | intron-variant | CADPS2 | GRCh38.p7 | 7:122813164 | TTATCCTAGAGAAAA[C/G]TGCAAGCTAATTATG | 93664 |
rs16870877 | snp | A/G/T | 0.0357623 | 0.129311 | intron-variant | CADPS2 | GRCh38.p7 | 7:122832482 | CCATCTCTGTCCAGC[A/G/T]GTCATTTGGAGATAT | 93664 |
rs16870879 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | CADPS2 | GRCh38.p7 | 7:122878751 | AAATTAATAAACTTA[C/T]AGACATACAACCTGT | 93664 |
rs17132789 | snp | C/T | 0.194902 | 0.243853 | intron-variant | CADPS2 | GRCh38.p7 | 7:122378891 | AGATCATCGCTTTCA[C/T]CAAAGGTATTTTGAG | 93664 |
rs17144227 | snp | C/T | 0.207253 | 0.246318 | intron-variant | CADPS2 | GRCh38.p7 | 7:122328715 | CTTGAGATATCTCTT[C/T]TAAAGCAAAAATAGA | 93664 |
rs17144249 | snp | C/G | 0.0150367 | 0.0853947 | intron-variant | CADPS2 | GRCh38.p7 | 7:122332636 | ACTTTCCTATCTTTG[C/G]CATTCCATACTTCAT | 93664 |
rs17144256 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CADPS2 | GRCh38.p7 | 7:122341715 | CTCTGAGTGGGAGAT[A/G]TTTTAACCTAAAAAT | 93664 |
rs17144272 | snp | A/G | 0.00297493 | 0.0384527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122345728 | TAATATCAGGTCTCA[A/G]TTGTGAAATTATTAT | 93664 |
rs17144296 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | CADPS2 | GRCh38.p7 | 7:122350229 | AGACAATAAATAACA[C/T]GTCTTCGAAATTTGA | 93664 |
rs17144315 | snp | A/G | 0.190205 | 0.242744 | intron-variant | CADPS2 | GRCh38.p7 | 7:122354062 | TGGCTGCTTTCTATA[A/G]GAGGAAGTAAAGTAA | 93664 |
rs17144328 | snp | A/C | 0.20111 | 0.245173 | intron-variant | CADPS2 | GRCh38.p7 | 7:122363795 | AATCACTATCTGTGT[A/C]TAAAAACCTGAATAC | 93664 |
rs17144333 | snp | C/G | 0.201418 | 0.245234 | intron-variant | CADPS2 | GRCh38.p7 | 7:122365128 | CTCATCTTCTTCAGA[C/G]CACGAAGCAGCATTG | 93664 |
rs17144341 | snp | A/G | 0.221141 | 0.248329 | intron-variant | CADPS2 | GRCh38.p7 | 7:122366262 | TATCATGAACTAGGA[A/G]AAAATAGGTTGTCTT | 93664 |
rs17144368 | snp | C/G | 0.18325 | 0.240924 | intron-variant | CADPS2 | GRCh38.p7 | 7:122390222 | TTCAGTGCCTCAAAT[C/G]CACCATTAAATAAGA | 93664 |
rs17144378 | snp | C/T | 0.442385 | 0.15965 | intron-variant | CADPS2 | GRCh38.p7 | 7:122390974 | TACAGATACATATGT[C/T]GATGAGCAATCCTTG | 93664 |
rs17144381 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122391844 | AGTTCTTAAACACAA[C/T]GTTCTATGACAGCAG | 93664 |
rs17144402 | snp | C/T | 0.00358165 | 0.0421663 | intron-variant | CADPS2 | GRCh38.p7 | 7:122416196 | CATAATCATGTTACC[C/T]TGAAAATAAAAAGCC | 93664 |
rs17144415 | snp | A/G | 0.0139853 | 0.0824443 | intron-variant | CADPS2 | GRCh38.p7 | 7:122426386 | TGCCAATCACTGTGA[A/G]TGTGTGTGCATGCAT | 93664 |
rs17144433 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CADPS2 | GRCh38.p7 | 7:122442826 | TATCATTGTATTTAC[C/T]GCTAAAAATGTCCTT | 93664 |
rs17144467 | snp | A/C | 0.408359 | 0.193449 | intron-variant | CADPS2 | GRCh38.p7 | 7:122458728 | TTAGGGTGCTGGTGA[A/C]TAGGCCAAGGACCAA | 93664 |
rs17144472 | snp | A/G | 0.170084 | 0.236883 | intron-variant | CADPS2 | GRCh38.p7 | 7:122461070 | AAAAATAGTTACAAG[A/G]TTTTGTATAGTTACA | 93664 |
rs17144504 | snp | C/T | 0.348794 | 0.229651 | intron-variant | CADPS2 | GRCh38.p7 | 7:122512711 | GCCAGTTAGTACAAA[C/T]ATATTTATATTAAAA | 93664 |
rs17144525 | snp | C/T | 0.182296 | 0.240658 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122533260 | ATTAATATAAAGCAG[C/T]AGTTAAAAAAATAGC | 93664 |
rs17144531 | snp | A/C | 0.167484 | 0.23599 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122534399 | CAGCAAAGTAACTAC[A/C]CAGAGGAGAGCAAAT | 93664 |
rs17144538 | snp | A/G | 0.181659 | 0.240478 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122535545 | ATTTTTATAAAGTCT[A/G]TTAAAGAACCTTTCC | 93664 |
rs17144588 | snp | G/T | 0.27008 | 0.249192 | intron-variant | CADPS2 | GRCh38.p7 | 7:122571454 | ATGCTGTGCATAATA[G/T]GATCAGCCCCTGTAA | 93664 |
rs17144625 | snp | C/T | 0.0113458 | 0.0744591 | missense, upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122621693 | TCTCCATATCTTTTG[C/T]TATAAATTTGGGGAA | 93664 |
rs17144645 | snp | A/G | 0.167158 | 0.235875 | intron-variant | CADPS2 | GRCh38.p7 | 7:122630273 | AACTACAAATTGACC[A/G]GGTTACATTTTTAAA | 93664 |
rs17144729 | snp | A/G | 0.179425 | 0.239831 | intron-variant | CADPS2 | GRCh38.p7 | 7:122693997 | AAGAGATTACTGAAG[A/G]ATTTTTCAACAGAAG | 93664 |
rs17144731 | snp | C/T | 0.173643 | 0.238054 | intron-variant | CADPS2 | GRCh38.p7 | 7:122696361 | GAAGAGCTCTTGTGA[C/T]TAACACAAAAGTCTC | 93664 |
rs17144752 | snp | C/T | 0.202651 | 0.245475 | intron-variant | CADPS2 | GRCh38.p7 | 7:122719638 | TAACTTCTGTCCATG[C/T]TACACCATCAAATGT | 93664 |
rs17144754 | snp | C/T | 0.18325 | 0.240924 | intron-variant | CADPS2 | GRCh38.p7 | 7:122728340 | AATAAACAACTGCAA[C/T]TATTTTTAAGTAAAT | 93664 |
rs17144768 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122738350 | AACTGTACACACAGG[A/G]GCATGTACTTCACTA | 93664 |
rs17144773 | snp | C/T | 0.030278 | 0.119257 | intron-variant | CADPS2 | GRCh38.p7 | 7:122739915 | ATGTACTATAAAACA[C/T]CTATATAGCAACTCA | 93664 |
rs17144793 | snp | C/G | 0.0528381 | 0.153711 | intron-variant | CADPS2 | GRCh38.p7 | 7:122751933 | AGTCCTTATTTACTC[C/G]CATTAGCATTTAGAA | 93664 |
rs17144794 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122752021 | ATCCACTCCATTTTA[C/T]AGGAGAAACTTGAAT | 93664 |
rs17144796 | snp | A/G | 0.102014 | 0.201495 | intron-variant | CADPS2 | GRCh38.p7 | 7:122752361 | CATACTTTCTGGAAG[A/G]GCTTTCTGAAATCCT | 93664 |
rs17144799 | snp | G/T | 0.030278 | 0.119257 | intron-variant | CADPS2 | GRCh38.p7 | 7:122752509 | ATTTAACACTAAAAT[G/T]GTTTGCATATTATAA | 93664 |
rs17144817 | snp | A/G | 0.304688 | 0.243945 | intron-variant | CADPS2 | GRCh38.p7 | 7:122764223 | TGAAGACCCTCTTAC[A/G]TGTTCCTACATCACC | 93664 |
rs17144819 | snp | A/G | 0.030278 | 0.119257 | intron-variant | CADPS2 | GRCh38.p7 | 7:122766790 | TAGCTGACAAGATAA[A/G]GAGTGACAGGTAACT | 93664 |
rs17144833 | snp | C/T | 0.030278 | 0.119257 | intron-variant | CADPS2 | GRCh38.p7 | 7:122770495 | TAACACAGTATCTGC[C/T]GCAACTCACAAGGTT | 93664 |
rs17144848 | snp | A/T | 0.0240643 | 0.107019 | intron-variant | CADPS2 | GRCh38.p7 | 7:122771386 | TACTATAATGAAGAC[A/T]ATGGGTGCTACTATA | 93664 |
rs17144854 | snp | A/G | 0.331179 | 0.236453 | intron-variant | CADPS2 | GRCh38.p7 | 7:122772194 | CCTATAAAAACATCC[A/G]CATTTGGTGATTACA | 93664 |
rs17144859 | snp | C/T | 0.348794 | 0.229651 | intron-variant | CADPS2 | GRCh38.p7 | 7:122780481 | AGACTATACATCTAA[C/T]ATTAATACCTCCAGG | 93664 |
rs17144864 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122784841 | GCCTTTTTACTTTGC[A/G]GGCCAAAATCTTTCT | 93664 |
rs17144867 | snp | G/T | 0.030278 | 0.119257 | intron-variant | CADPS2 | GRCh38.p7 | 7:122786352 | AGACACTGGGATAAA[G/T]GACTGATCAGATAAT | 93664 |
rs17144881 | snp | C/T | 0.297128 | 0.245518 | intron-variant | CADPS2 | GRCh38.p7 | 7:122787659 | AGTAATTAATGTAAG[C/T]GCCTAGTGCAATGCA | 93664 |
rs17144891 | snp | A/T | 0.306679 | 0.24349 | intron-variant | CADPS2 | GRCh38.p7 | 7:122789776 | GAAACCAAAAATAAA[A/T]CATAACACACTGTTT | 93664 |
rs17144897 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | CADPS2 | GRCh38.p7 | 7:122799937 | ACTTGGCCACTTACA[A/G]GCTATGTGACTGTTG | 93664 |
rs17144900 | snp | A/C | 0.030278 | 0.119257 | intron-variant | CADPS2 | GRCh38.p7 | 7:122802176 | CTTCTATTTTGGAGG[A/C]CTCTATACTGTAAAT | 93664 |
rs17144901 | snp | C/T | 0.297128 | 0.245518 | intron-variant | CADPS2 | GRCh38.p7 | 7:122803594 | CTTGTGGCTTGGCAG[C/T]TCATGCCTCTGATCA | 93664 |
rs17144907 | snp | G/T | 0.337158 | 0.234315 | intron-variant | CADPS2 | GRCh38.p7 | 7:122806531 | TAAATATTTTAAGAT[G/T]TCTAAAAAACAAATT | 93664 |
rs17144922 | snp | A/T | 0.311369 | 0.242351 | intron-variant | CADPS2 | GRCh38.p7 | 7:122810628 | AATATAACCATTTAT[A/T]CGCAGGATTTTATCT | 93664 |
rs17144926 | snp | C/T | 0.311123 | 0.242413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122811153 | CATTTTCTGAACATA[C/T]GCTGTCCACAGGCAA | 93664 |
rs17144928 | snp | A/G | 0.331179 | 0.236453 | intron-variant | CADPS2 | GRCh38.p7 | 7:122811369 | TCAGCAAAATAACAC[A/G]GCTATAAAATTATCT | 93664 |
rs17144934 | snp | C/T | 0.311123 | 0.242413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122812224 | AAAAGAGTTTCATGA[C/T]CCATTGATAGAAAAC | 93664 |
rs17144935 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122812297 | AATGTTGTAAAACTT[C/T]GAACAATGCTAAAGC | 93664 |
rs17144937 | snp | A/C | 0.311614 | 0.242289 | intron-variant | CADPS2 | GRCh38.p7 | 7:122812866 | AAGTAACTACAGTGC[A/C]CTAGTACAAACTTAC | 93664 |
rs17144940 | snp | C/G | 0.311123 | 0.242413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122813365 | TATATGAACAACCTA[C/G]AGTAATTATATTTTT | 93664 |
rs17144942 | snp | G/T | 0.304937 | 0.243889 | intron-variant | CADPS2 | GRCh38.p7 | 7:122815271 | TCATCTACTAGAGAT[G/T]CACTCCTAACCAAAA | 93664 |
rs17144945 | snp | G/T | 0.310878 | 0.242475 | intron-variant | CADPS2 | GRCh38.p7 | 7:122815317 | ATTTGCTTCTGGCAA[G/T]AAATGTGCCTAGGTC | 93664 |
rs17144947 | snp | C/T | 0.311123 | 0.242413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122815385 | ATACTGCTTTTATCC[C/T]ACATCTGGAAAAGCC | 93664 |
rs17144949 | snp | C/T | 0.311123 | 0.242413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122815428 | TTTCACAAAGCCTTA[C/T]CTCAGAAAAGTTCAT | 93664 |
rs17144969 | snp | G/T | 0.32955 | 0.237006 | intron-variant | CADPS2 | GRCh38.p7 | 7:122831327 | TGCTGTCATTTGGGT[G/T]TTTTCGCTCAACTGG | 93664 |
rs17144992 | snp | C/T | 0.258565 | 0.249853 | intron-variant | CADPS2 | GRCh38.p7 | 7:122832966 | TGTGAATACATTTCT[C/T]GTCTTTAACTGCAGA | 93664 |
rs17144996 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | CADPS2 | GRCh38.p7 | 7:122833829 | GCACCCTTAAAAAAT[C/T]CACCTCAATAGCATT | 93664 |
rs17145002 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | CADPS2 | GRCh38.p7 | 7:122843044 | ACACAAGGGAAAAAA[C/T]GCTTTAATCTCATAT | 93664 |
rs17145014 | snp | G/T | 0.312593 | 0.242037 | intron-variant | CADPS2 | GRCh38.p7 | 7:122845243 | TCTTTGGGCCCAGGT[G/T]TGTGTGTGCTAAGAT | 93664 |
rs17145022 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122845929 | AGCGTTATGATTGCT[C/T]GCCAACACGGTGGTC | 93664 |
rs17145025 | snp | C/G | 0.0425829 | 0.139564 | intron-variant | CADPS2 | GRCh38.p7 | 7:122852998 | AAAATGTTAATGATA[C/G]AAAGTGCATTAGGGA | 93664 |
rs17145052 | snp | A/C | 0.323197 | 0.239044 | intron-variant | CADPS2 | GRCh38.p7 | 7:122862068 | AGGCTCCAATTCAAA[A/C]GAATTATGAAGAAAT | 93664 |
rs17145065 | snp | A/G | 0.331411 | 0.236373 | intron-variant | CADPS2 | GRCh38.p7 | 7:122873035 | AGCTCCAGGAAAGGA[A/G]TACAGAAATGCCCTT | 93664 |
rs17145068 | snp | C/T | 0.242775 | 0.249896 | intron-variant | CADPS2 | GRCh38.p7 | 7:122875603 | AAGTACCATAAGCAA[C/T]ATTCTCTGTCAACCT | 93664 |
rs17364956 | snp | C/T | 0.154329 | 0.23097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122349303 | GTAATCATAGTTTTC[C/T]TAATATGAGAAAAAT | 93664 |
rs17365158 | snp | A/G | 0.154661 | 0.231107 | intron-variant | CADPS2 | GRCh38.p7 | 7:122350681 | ATAAATATGATGGGA[A/G]GAGAAACAGTTGATA | 93664 |
rs17365759 | snp | A/G | 0.14665 | 0.227637 | intron-variant | CADPS2 | GRCh38.p7 | 7:122367081 | TGCTATTCCTTTTGG[A/G]CACATACTTGGATTT | 93664 |
rs17366412 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122411947 | ATGATGAGCTGAAAA[C/T]GCTCCAAAACATGAG | 93664 |
rs17369598 | snp | A/G | 0.221141 | 0.248329 | intron-variant | CADPS2 | GRCh38.p7 | 7:122325383 | TAAGTGATACTTTTT[A/G]GTTACATCAAATACA | 93664 |
rs17380636 | snp | C/T | 0.0748431 | 0.178382 | intron-variant | CADPS2 | GRCh38.p7 | 7:122506420 | AGGTTTCAGCATCAC[C/T]GCTTTTGATAGGGCA | 93664 |
rs17381160 | snp | G/T | 0.203882 | 0.245709 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122542531 | AACAAATGGGAACTT[G/T]TCTTTCTATAAATAA | 93664 |
rs17381305 | snp | C/T | 0.204803 | 0.245881 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122546502 | CCATGTCCTATCCTT[C/T]GCTATGTTCCATAAA | 93664 |
rs17381596 | snp | G/T | 0.204189 | 0.245767 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122551551 | AAAGATCTATTTGAC[G/T]TCCACATTATTAAAA | 93664 |
rs17381814 | snp | G/T | 0.20511 | 0.245937 | intron-variant | CADPS2 | GRCh38.p7 | 7:122572495 | GTAGAAATGTTTTTA[G/T]AGCAAAATTTCTAAA | 93664 |
rs17381835 | snp | C/T | 0.204803 | 0.245881 | intron-variant | CADPS2 | GRCh38.p7 | 7:122572526 | ATGAAAGAAAAGTTA[C/T]TTTGGCAAACCCTCC | 93664 |
rs17461878 | snp | C/T | 0.134119 | 0.221521 | intron-variant | CADPS2 | GRCh38.p7 | 7:122341867 | TATTATTTTGATAGG[C/T]TGAAAAGATGAAGGA | 93664 |
rs17462032 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | CADPS2 | GRCh38.p7 | 7:122343599 | AGTAAATAGGTCACC[A/G]AGTCAAAAAACTGAA | 93664 |
rs17462307 | snp | A/G | 0.147321 | 0.227941 | intron-variant | CADPS2 | GRCh38.p7 | 7:122348926 | ATAGAAGACATTATC[A/G]CTGGTTCAATGCTCC | 93664 |
rs17462383 | snp | C/T | 0.154329 | 0.23097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122349647 | ACACTGTATAAGTAA[C/T]CAAATACATCAGTGA | 93664 |
rs17462418 | snp | C/T | 0.154329 | 0.23097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122349733 | CACTAGTTAACCTAG[C/T]AAGATGAACACGCTG | 93664 |
rs17462508 | snp | C/T | 0.147321 | 0.227941 | intron-variant | CADPS2 | GRCh38.p7 | 7:122350142 | GTTATGATTATCTGC[C/T]TGCTTTGTAAATGAA | 93664 |
rs17462571 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122351977 | TATTAAAATAAATAC[C/T]GAATGATAGTTTAAG | 93664 |
rs17462732 | snp | A/G | 0.282895 | 0.247826 | intron-variant | CADPS2 | GRCh38.p7 | 7:122355016 | TTCAGGACTACACTG[A/G]AGCATTTTTCTCCTA | 93664 |
rs17463004 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | CADPS2 | GRCh38.p7 | 7:122365785 | CTCATGAAACTCTTG[A/G]AAGTGACTGGTAGAA | 93664 |
rs17463319 | snp | A/G | 0.29278 | 0.246313 | intron-variant | CADPS2 | GRCh38.p7 | 7:122370985 | TAGGAATTCCAGAAT[A/G]AAGGGCCCCAGGACA | 93664 |
rs17463779 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | CADPS2 | GRCh38.p7 | 7:122411591 | GGATGGCTGCCTAAA[C/T]GAGCAAAAACAGTGA | 93664 |
rs17463849 | snp | A/T | 0.0456336 | 0.143994 | intron-variant | CADPS2 | GRCh38.p7 | 7:122412070 | TTTGACAGTCACTGC[A/T]GAAATGGGAATTCTA | 93664 |
rs17465881 | snp | A/C | 0.203882 | 0.245709 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122542486 | TATTAAATGTTCATA[A/C]CTTTCATTTTAAGAT | 93664 |
rs17465937 | snp | C/T | 0.203575 | 0.245652 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122543083 | TTTTTTTTTAATAAT[C/T]TGTGAATTCTGGTAT | 93664 |
rs17610847 | snp | A/G | 0.111928 | 0.208413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122809995 | TCAAATGAGCTGGAA[A/G]ACAGTTCATGGTGTA | 93664 |
rs17611216 | snp | C/T | 0.0821764 | 0.185298 | intron-variant | CADPS2 | GRCh38.p7 | 7:122813570 | TGAGTCTTTCAAATG[C/T]AGAAATGTTCTTAAA | 93664 |
rs17611963 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | CADPS2 | GRCh38.p7 | 7:122880289 | GTGGTGATTTATCTA[C/T]AGTTGTACAATGAAT | 93664 |
rs17682388 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122700313 | TAAATCTACAACATG[A/G]TAATTTGAGACAAGA | 93664 |
rs17682540 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | CADPS2 | GRCh38.p7 | 7:122713839 | TTTATAGTTATAATG[C/T]ACAGGCCAACTTTAA | 93664 |
rs17683699 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | CADPS2 | GRCh38.p7 | 7:122791398 | TTCTAATCTTCCATG[A/G]GTCATTTTCTTTGAT | 93664 |
rs17683741 | snp | G/T | 0.0391387 | 0.134304 | intron-variant | CADPS2 | GRCh38.p7 | 7:122800185 | AAACATCCACGGTTA[G/T]AATACTAGTTTTATT | 93664 |
rs17684127 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | CADPS2 | GRCh38.p7 | 7:122813039 | ACACAGCAGGAAAAG[C/G]CTCAATAACAGGACT | 93664 |
rs17684427 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | CADPS2 | GRCh38.p7 | 7:122842923 | AAATAAGCTAGGGAG[A/C]CTTCAAAGCCTTTCA | 93664 |
rs28379593 | snp | A/G | 0.193028 | 0.243422 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122559965 | AGGTAGTAGGAAGGG[A/G]GCATCAGGGTCACAT | 93664 |
rs28380284 | snp | C/T | 0.118933 | 0.212888 | intron-variant | CADPS2 | GRCh38.p7 | 7:122457698 | GTGCTGACGAGCATC[C/T]GTTCTATTACTTAAT | 93664 |
rs28390321 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122471159 | CTCTCTCTCTCTTTC[A/G]AGTGGCTTTACCAGC | 93664 |
rs28393630 | snp | A/G | 0.0535932 | 0.154675 | intron-variant, upstream-variant-2KB | CADPS2, LOC105375481 | GRCh38.p7 | 7:122528523 | TGTATCTTTATTTAG[A/G]GGAGAATGAATAACT | 93664 |
rs28397617 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122588196 | AGTTTCTTTTGCTGT[A/G]CAGAAGCTCTTTAGT | 93664 |
rs28399134 | snp | A/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122540107 | TTTAGTCTAGAATTT[A/T]AAAAGTCCACTGAAT | 93664 |
rs28399243 | snp | G/T | 0.118584 | 0.212673 | intron-variant | CADPS2 | GRCh38.p7 | 7:122404173 | ACAGGCCCCAGTGTG[G/T]GATGTTCCCCTTCCT | 93664 |
rs28403443 | snp | G/T | 0.0618563 | 0.164627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122712410 | CTACATTATTGATTA[G/T]TTCACTCATTCGAAT | 93664 |
rs28406245 | snp | C/T | 0.0763149 | 0.179815 | intron-variant | CADPS2 | GRCh38.p7 | 7:122453583 | CTGAATATCCCTAGG[C/T]AAATTGATAAAAAGA | 93664 |
rs28408353 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122532064 | ACAAACAAACAAACA[A/G]AATACTGTTAGCCTG | 93664 |
rs28409732 | snp | A/C | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122537572 | AAATAAAAACAAAAA[A/C]AAAAATTTCATATTA | 93664 |
rs28415072 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | CADPS2 | GRCh38.p7 | 7:122517399 | TAGGCATGTCTTCAT[C/T]TCTCCTGGGTAAATA | 93664 |
rs28415980 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | CADPS2 | GRCh38.p7 | 7:122588805 | ACTGTGTTATTTTCA[C/T]TGACTCATATTTGGT | 93664 |
rs28416120 | snp | C/G | 0.029116 | 0.117091 | intron-variant | CADPS2 | GRCh38.p7 | 7:122491910 | TAAAAAAAGATCTCA[C/G]GCCTGTAATCCCAGC | 93664 |
rs28417719 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122443707 | TCCAGTTTCTGCTTT[C/T]TACAAAAAAAAAAAA | 93664 |
rs28421882 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122461519 | AAGAATCTTTTTTTA[A/T]AAAAAGCATCCAGAG | 93664 |
rs28431138 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122714484 | CTATCATCATTTTTT[A/T]AAAAAAACAAACAAT | 93664 |
rs28433750 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | CADPS2 | GRCh38.p7 | 7:122403824 | TCCATTGTAGATGAA[C/T]GGAATATCATCAAAA | 93664 |
rs28434287 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122856037 | GGAGCCCATGGCCCC[C/T]TCCCCCTTCCTTCTG | 93664 |
rs28438469 | snp | A/C/G | 0.0158469 | 0.0875917 | intron-variant | CADPS2 | GRCh38.p7 | 7:122451062 | TTACCTGGTAATACA[A/C/G]AGAGCAGGAGGAACA | 93664 |
rs28449483 | snp | A/G | 0.0711525 | 0.174681 | intron-variant | CADPS2 | GRCh38.p7 | 7:122693161 | AAAATTCCATGTGAC[A/G]CTCAAAGCTCCTTTA | 93664 |
rs28450014 | snp | A/T | 0.0349115 | 0.127424 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122557001 | ATATCTAATTCCCTA[A/T]GTTATGTTCCCTCCA | 93664 |
rs28459977 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | CADPS2 | GRCh38.p7 | 7:122680512 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 93664 |
rs28479518 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122803883 | AATTTCTCTAGGGGA[G/T]GGGTTACTTAATAAA | 93664 |
rs28487917 | snp | A/G | 0.0733688 | 0.176922 | intron-variant | CADPS2 | GRCh38.p7 | 7:122499495 | CACTATATTTTATTC[A/G]GCATTTCTAGGTATT | 93664 |
rs28492775 | snp | C/T | 0.077417 | 0.180873 | intron-variant | CADPS2 | GRCh38.p7 | 7:122456501 | TATATGAAAAAATTA[C/T]AAAACAGATTAAAAT | 93664 |
rs28493239 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122527296 | GGGCTCTTCAACCAC[C/T]GCTGAAAATGGCTTC | 93664 |
rs28514506 | snp | C/T | 0.373799 | 0.217195 | intron-variant | CADPS2 | GRCh38.p7 | 7:122522986 | TTGTTGATAAACAGG[C/T]TGATTTCATATGTTG | 93664 |
rs28517374 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | CADPS2 | GRCh38.p7 | 7:122629639 | CTTGTTTTGTTCTTT[C/T]AAGTTCTCACCATGT | 93664 |
rs28522818 | snp | A/G | 0.0744748 | 0.178019 | intron-variant | CADPS2 | GRCh38.p7 | 7:122496442 | TGCTGGGATTATGGC[A/G]TGAGTCACCACGCCT | 93664 |
rs28538086 | snp | A/T | 0.135143 | 0.222054 | intron-variant | CADPS2 | GRCh38.p7 | 7:122460239 | TTGTCCAGCTCTTAC[A/T]AGAAAGTAAAATAAT | 93664 |
rs28540575 | snp | C/T | 0.318896 | 0.240319 | intron-variant | CADPS2 | GRCh38.p7 | 7:122681693 | AAGACTGAAGACAGG[C/T]TATTCTCTGGAGAAA | 93664 |
rs28541748 | snp | A/T | | | intron-variant | CADPS2, RNF148 | GRCh38.p7 | 7:122701465 | GAAGCGGGGAGGGAT[A/T]GCATTTGGAGATATA | 93664 |
rs28547074 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | CADPS2 | GRCh38.p7 | 7:122709322 | TGCTCATCATCACTG[A/G]CCATCAGAGAAATGC | 93664 |
rs28547519 | snp | C/T | 0.469148 | 0.120308 | intron-variant | CADPS2 | GRCh38.p7 | 7:122324564 | CCCAGGTGATGATGA[C/T]AGTGGTAGGTGAGGA | 93664 |
rs28550991 | snp | C/T | 0.0711525 | 0.174681 | intron-variant | CADPS2 | GRCh38.p7 | 7:122693918 | GCAGTAAGCCAAGAT[C/T]GTGCCACTGCACTCC | 93664 |
rs28555167 | snp | A/C | 0.125528 | 0.21681 | intron-variant | CADPS2 | GRCh38.p7 | 7:122441394 | GTGAGAAACTCATGA[A/C]TTGTGATGGAATCAG | 93664 |
rs28565406 | snp | A/G | 0.282369 | 0.247896 | intron-variant | CADPS2 | GRCh38.p7 | 7:122586238 | CTAGTGTGAGCAACC[A/G]AAGTCCCTATCCCCT | 93664 |
rs28572499 | snp | A/C | 0.0283406 | 0.115616 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122540355 | AAATACTGTGAATTC[A/C]ATTTTTCAAGTTGAA | 93664 |
rs28595282 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122441866 | AAGGGTCATGAGTAA[A/G]GCGATAATATGCATT | 93664 |
rs28625932 | snp | A/C | 0.0689305 | 0.172377 | intron-variant | CADPS2 | GRCh38.p7 | 7:122497578 | ATTATATTAGTTCTA[A/C]CTTATTTTAGTAATG | 93664 |
rs28626173 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | CADPS2 | GRCh38.p7 | 7:122344432 | TGACTGCTCTGTTAG[C/T]CTCCTTTACAGATAC | 93664 |
rs28630520 | snp | A/G | 0.114738 | 0.210248 | intron-variant | CADPS2 | GRCh38.p7 | 7:122394636 | CAAACAAGTTTTGGG[A/G]AGGAATAAGCTTGGG | 93664 |
rs28635203 | snp | C/T | 0.0901694 | 0.192235 | intron-variant | CADPS2 | GRCh38.p7 | 7:122678461 | ATTACTCAAATTAAT[C/T]TCTCAAAGGCTTGGA | 93664 |
rs28636803 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122409348 | AAAGGTTAAAATTAA[A/G]AAAATAACAGTCATG | 93664 |
rs28642148 | snp | C/T | 0.319376 | 0.240181 | intron-variant | CADPS2 | GRCh38.p7 | 7:122681457 | ACATAGTGGAGGCCG[C/T]AGCAGTCAGGGACAT | 93664 |
rs28648607 | snp | A/C | 0.145978 | 0.227331 | intron-variant | CADPS2 | GRCh38.p7 | 7:122462088 | AGGAAAGTCCAAAGA[A/C]CATTCTTCAGAAAAA | 93664 |
rs28648932 | snp | A/G | 0.0818113 | 0.184966 | intron-variant | CADPS2 | GRCh38.p7 | 7:122462301 | GTTAATTAGCATAAG[A/G]CTTTAAAATTTCAGC | 93664 |
rs28651256 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | CADPS2 | GRCh38.p7 | 7:122521608 | AGGCTTGAATTATTA[C/T]GGGAAACAGTAAAAG | 93664 |
rs28655884 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122772443 | CAAAATTTTAAAATG[C/T]CACTTTACTTTTAGA | 93664 |
rs28657411 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122619459 | CTTTACTAAAAAATA[A/C]AAAAAAAAAAAAAAA | 93664 |
rs28671172 | snp | G/T | 0.269809 | 0.249214 | intron-variant | CADPS2 | GRCh38.p7 | 7:122575272 | GATTCTATCCTAGAC[G/T]GGGGGAGAATACCAG | 93664 |
rs28684792 | snp | A/G | 0.0818113 | 0.184966 | intron-variant | CADPS2 | GRCh38.p7 | 7:122461886 | GGTGTGAGCCACCTC[A/G]CCTGGCCTGCCAAGA | 93664 |
rs28700913 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122504036 | GGAAGATAAACCAGG[C/T]TTAACAGATCAATCT | 93664 |
rs28712478 | snp | A/T | 0.134802 | 0.221877 | intron-variant | CADPS2 | GRCh38.p7 | 7:122460593 | TCTTAAGTATAAATG[A/T]TTATTACAAAAAAAT | 93664 |
rs28718556 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122537658 | CAACTCAAGGATTTG[A/G]AAAAAACACAACCCA | 93664 |
rs28722960 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122574160 | AAAAAATGTGTATTT[C/T]TTGGGCTGGGAACAG | 93664 |
rs28729738 | snp | C/T | 0.029116 | 0.117091 | intron-variant | CADPS2 | GRCh38.p7 | 7:122460434 | GCTAAGCCTGAGACA[C/T]CTGCATAAAAATGGG | 93664 |
rs28735372 | snp | G/T | 0.081446 | 0.184634 | intron-variant | CADPS2 | GRCh38.p7 | 7:122462256 | AGGGTAATATTCTAA[G/T]GACTCTGAACTACCT | 93664 |
rs28744527 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | CADPS2 | GRCh38.p7 | 7:122377760 | ATTATTTTTTTCTCT[A/G]TCTATCCACTTGTTG | 93664 |
rs28756115 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122743459 | GCTGCATGGAGCCTG[A/C]CCTGACCTGCAGAAC | 93664 |
rs28848479 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122444510 | GAATTTAACTATACC[A/C]CTAAGTATGCAGTGG | 93664 |
rs28871653 | snp | C/G | 0.202959 | 0.245534 | intron-variant | CADPS2 | GRCh38.p7 | 7:122722552 | AAAAAAGGACACAAA[C/G]AAATGGAAGAACATT | 93664 |
rs28879744 | snp | A/G | 0.21845 | 0.248001 | intron-variant | CADPS2 | GRCh38.p7 | 7:122722425 | AGAGCCAAATCATGA[A/G]TGAACTCCCATTCAC | 93664 |
rs33914995 | in-del | -/A/AT/T/TA | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122756226 | CAAGGACTTAATTAA[-/A/AT/T/TA]ATATATATATTGGTA | 93664 |
rs33958352 | in-del | -/AAAAA | 0.406296 | 0.19512 | intron-variant | CADPS2 | GRCh38.p7 | 7:122437809 | AAAGCCTGAAGAAAG[-/AAAAA]AAAAAAAAGCACAGT | 93664 |
rs33997607 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122652575 | TATTCTTCCTTCACT[-/C]CCTGTTCCTTTTTAT | 93664 |
rs33998785 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122878001 | TACTGCACTATTTTT[-/A]AAAAAGTGGCACTTT | 93664 |
rs34001470 | in-del | -/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122533921 | TCAATTACAAATAAT[-/G]GGGGTGTATGAGAGA | 93664 |
rs34004184 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122614905 | AATTTGCTTTCCTTA[A/G]AAATGACTTATAAAT | 93664 |
rs34005451 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122607165 | AGGGACTAAAGTCCC[-/T]TTTTTCCCACTACAG | 93664 |
rs34006020 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122668402 | AGACAAAGTATGGTT[-/A]AAAAAAAAAAAAAAA | 93664 |
rs34009656 | snp | A/T | 0.241627 | 0.24986 | intron-variant | CADPS2 | GRCh38.p7 | 7:122616650 | AAATCAGGACTTAAC[A/T]GAAAACAGACTAAGA | 93664 |
rs34009703 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122581369 | GTCTCCATAGAAGGC[A/C]AATTAAATACAGAAT | 93664 |
rs34027824 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122822639 | GTAACTGAAGAATCA[C/T]AAAAGAAGTGAATAT | 93664 |
rs34031054 | in-del | -/A | 0.310878 | 0.242475 | intron-variant | CADPS2 | GRCh38.p7 | 7:122815619 | GTAATAATGAAATAC[-/A]AAAAAAATTCAAAAT | 93664 |
rs34052520 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122633920 | TTGGACTTTATTGAA[-/G]GCTTTTTCTGCATCT | 93664 |
rs34074704 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122452284 | TGTTAGTGCAGAGGG[-/A]AAAAAAGTATGAATC | 93664 |
rs34080149 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | CADPS2 | GRCh38.p7 | 7:122859643 | CTTTGTTATCCATGA[A/G]GGATAGGTTCCAGGA | 93664 |
rs34082235 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122710049 | AACTTAAAGTATAAT[-/A]AAAAAAAAAAAAAAA | 93664 |
rs34089631 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | CADPS2 | GRCh38.p7 | 7:122668985 | CAACTTTGTTTTGTT[C/T]GCTAATAAATCCAGT | 93664 |
rs34101178 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122369388 | CGCCTGCCTCAGCCT[-/C]CCAAAGTGCTGGGAT | 93664 |
rs34102364 | snp | C/T | 0.330947 | 0.236533 | intron-variant | CADPS2 | GRCh38.p7 | 7:122842141 | TTTGGCTCAGGAACA[C/T]GGCCCACTTCAGATG | 93664 |
rs34125908 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | CADPS2 | GRCh38.p7 | 7:122662453 | CGATCTCAGCTCACT[A/G]CAACCTCCGCCTCCC | 93664 |
rs34133916 | snp | C/T | 0.0748431 | 0.178382 | intron-variant | CADPS2 | GRCh38.p7 | 7:122472611 | TCCATATTACACTGG[C/T]GGTCAACAACAAAAT | 93664 |
rs34139476 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122330200 | TTAAAATGAAATAAC[-/G]GCCAAGAAAATCTCA | 93664 |
rs34148286 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122670195 | ATATATATATAAACA[C/T]TGATCATTTAAATCC | 93664 |
rs34162803 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122799502 | AGCTACTTGGGAGGC[-/G]TGAGGCGGGAGAATG | 93664 |
rs34176184 | in-del | -/AT | 0.303688 | 0.244167 | intron-variant | CADPS2 | GRCh38.p7 | 7:122684436 | AAGTTTGTAGTAAGC[-/AT]ATATATATATATACA | 93664 |
rs34179141 | in-del | -/A/AA | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122651274 | AGGCTACTAGTTGGA[-/A/AA]AAAAAAAAAAAAAAA | 93664 |
rs34182273 | in-del | -/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122484667 | AAAATTAAGAATTTC[-/T]TTTTTTTTTTTTCTG | 93664 |
rs34182275 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | CADPS2 | GRCh38.p7 | 7:122631092 | ACTGAAATCTCTCAT[C/T]CCAAGCTCCTAAAAA | 93664 |
rs34186344 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122816039 | TTCCAATTCCACTGT[-/G]TTTAGTTATGTTGAA | 93664 |
rs34194021 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122859552 | ACTATTAAGTCACTC[-/A]AAAACAAAATGAAAA | 93664 |
rs34197810 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122377893 | CTTTGTGGTTGTTTT[-/C]CCACTCTAAGACATG | 93664 |
rs34202731 | in-del | -/T | 0.496583 | 0.0411924 | intron-variant | CADPS2 | GRCh38.p7 | 7:122801779 | TTTAATTTTTATTTA[-/T]TTTTTTTTTCTGGAG | 93664 |
rs34208874 | snp | C/T | 0.261056 | 0.249755 | intron-variant | CADPS2 | GRCh38.p7 | 7:122615110 | ATTTATGCACATAAA[C/T]AGAGCATGTTTCTTT | 93664 |
rs34211190 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122415181 | TTAATTCAAAAAAGT[-/G]GAAAAGTTCAATGTT | 93664 |
rs34215804 | in-del | -/C | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122551552 | AGATCTATTTGACGT[-/C]CCACATTATTAAAAC | 93664 |
rs34217280 | in-del | -/T | 0.375 | 0.216506 | intron-variant | CADPS2 | GRCh38.p7 | 7:122669356 | ATATATATATATATA[-/T]TTTTTTTTTTTGAGA | 93664 |
rs34217651 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122390803 | CATTTTAAAATTATT[-/G]TCTAATTGGTGGCCT | 93664 |
rs34221727 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122365363 | CTGAGGTGTACAGTT[-/C]CCTACAGGAAAGTTT | 93664 |
rs34235307 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122337078 | ATGTCAGAGCTGCAA[-/G]GGCTACATCTCCCTA | 93664 |
rs34239286 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122481741 | TACAGGCAGGTGCAG[C/T]GGCTCATGCCTGTAA | 93664 |
rs34249417 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122687776 | GATACTACAAATTCA[-/G]GGGAGCCAAAAATAG | 93664 |
rs34252702 | snp | A/T | 0.0479149 | 0.147179 | intron-variant | CADPS2 | GRCh38.p7 | 7:122408870 | TATGGCCTTAAAATA[A/T]TAGATATAAAATAAT | 93664 |
rs34259254 | in-del | -/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122558110 | TTGAAATGTAACGAC[-/T]TTTCTTGTTATAGCA | 93664 |
rs34264090 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | CADPS2 | GRCh38.p7 | 7:122641328 | TATTTAGTTCAGAAA[A/G]TATGCTTTTATTTTC | 93664 |
rs34279868 | snp | C/T | 0.166506 | 0.235645 | intron-variant | CADPS2 | GRCh38.p7 | 7:122575686 | AGGTGATCTGCCTGC[C/T]TCGGCCTCCCAAAGT | 93664 |
rs34283322 | snp | C/T | 0.182296 | 0.240658 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122534931 | GGAGGGATGTTTCTA[C/T]AAACCAAAAAATAAA | 93664 |
rs34283462 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122599164 | GGACACAGGCCAGGG[-/G]AAGTTCAATAACTCC | 93664 |
rs34283534 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122776305 | TGCCATGTAAGACAT[-/G]GCCTTTGCTCTTCCT | 93664 |
rs34286191 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122871342 | ATTTGCAGGATACTT[-/C]ATGATCTTGATCTCA | 93664 |
rs34288982 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122783939 | TTCCAAGAGGGCTTG[A/C]GGCTATTACTATAAC | 93664 |
rs34290652 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122375819 | TCAACATAATGAAAA[-/G]GGCAACCTACAAAAT | 93664 |
rs34290734 | in-del | -/T/TT/TTT | 0.315758 | 0.241197 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122541362 | CACCACACCCAGCTA[-/T/TT/TTT]TTTTTTTTTTTTTTT | 93664 |
rs34296287 | snp | A/T | 0.311123 | 0.242413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122809372 | CAAGAGTTCAAGACC[A/T]GCCTGGCCAAGATGG | 93664 |
rs34300133 | in-del | -/A | 0.0197687 | 0.0974348 | intron-variant | CADPS2 | GRCh38.p7 | 7:122720921 | TTCATATGGTTTAAC[-/A]AAAAAAGCTATCATT | 93664 |
rs34318072 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122786838 | AAATGCTCACACTGG[-/A]AAAAAAAGATGTGTG | 93664 |
rs34321994 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122439234 | TATTTATAAACACTG[-/T]TTACATTGACTCATA | 93664 |
rs34328604 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122578145 | CTTTTGTATATACTT[-/A]AATATGTGTATATAT | 93664 |
rs34333754 | in-del | -/T | 0.375 | 0.216506 | intron-variant | CADPS2 | GRCh38.p7 | 7:122443591 | TTTTTAAATACAGTA[-/T]TTTTTTTTTTTACCA | 93664 |
rs34334958 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122720696 | TTTTAATATACCCCT[-/A]AAAAGGATATACCTC | 93664 |
rs34336507 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122852092 | TCAAAAATTTAAGTG[-/A]AAAAGTTTTTTTCTA | 93664 |
rs34337259 | in-del | -/AA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122768554 | AAAACCGTATCAGAC[-/AA]AGAGGATTCTGACTT | 93664 |
rs34346263 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122466132 | TATGTCAAGGTGTAA[-/C]CCCTTGTTTCTGTTC | 93664 |
rs34347947 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122765443 | AATTAATGAGTACAT[-/G]GGATAAATGACTGAG | 93664 |
rs34352216 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122431952 | GGGGAGGGAAACAAA[G/T]AAGTAAATTAGTTGA | 93664 |
rs34359450 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122469979 | ACTTTTTAAAACTGG[-/A]AAAAAGAAAAACATG | 93664 |
rs34360995 | in-del | -/AA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122527417 | TCTCACTAATATGCT[-/AA]AAAAAAAAAAAACAC | 93664 |
rs34376614 | snp | A/T | 0.16976 | 0.236773 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122538375 | TTTGTTTTTTTTTTT[A/T]AAAAACACAAGGAGA | 93664 |
rs34377083 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122738215 | GCTACTTAATTTGTA[-/G]GGGCCCAGTGCAAAA | 93664 |
rs34381122 | snp | C/T | 0.299664 | 0.245017 | intron-variant | CADPS2 | GRCh38.p7 | 7:122809561 | CTCCAGCCTGGGCAA[C/T]AGAGAGAGACACTGT | 93664 |
rs34382409 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122440798 | AAATTCATTTTAATT[C/T]TGGTAAGAAATGGGA | 93664 |
rs34388214 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122415528 | TTATGGAATTATGAG[-/A]AGAAATAGAGTGAGA | 93664 |
rs34393979 | snp | A/G | 0.16028 | 0.233346 | intron-variant | CADPS2 | GRCh38.p7 | 7:122640062 | TCAGCTCCGTACCCC[A/G]ATCATTCATGAGTAA | 93664 |
rs34416261 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122527267 | AGCCCCTTTATGCCG[-/A]AAAGGGACTTCCAGG | 93664 |
rs34419881 | multinucleotide-polymorphism | AC/GG | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122718661 | GGGAACTGATCAAAT[AC/GG]GGCCGTGTTAAGGCT | 93664 |
rs34420222 | snp | C/G | 0.0460142 | 0.144533 | intron-variant | CADPS2 | GRCh38.p7 | 7:122641058 | AGGTAAGGCTTCACT[C/G]TACCAAGGCAATTTC | 93664 |
rs34421933 | in-del | -/TA/TATA | 0.369239 | 0.24668 | intron-variant | CADPS2 | GRCh38.p7 | 7:122366685 | ATATATATATATACG[-/TA/TATA]TATATATATATATAC | 93664 |
rs34427116 | snp | G/T | 0.0448719 | 0.142907 | intron-variant | CADPS2 | GRCh38.p7 | 7:122498368 | ATTGTATTTCTTATA[G/T]CTGATAATTCATGAC | 93664 |
rs34433720 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122326976 | GATAAATAAAAGCTT[-/G]CAAGTTTTAAAAATG | 93664 |
rs34434444 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122461438 | ATATATGTCCCAATC[A/C]CAATAAATTAAAAGA | 93664 |
rs34434974 | snp | A/C | 0.375996 | 0.215928 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122532040 | CGTCTCAAAAAAAAA[A/C]AAAACAAAACAAACA | 93664 |
rs34449869 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122832441 | AATGTGGTGACATTC[-/A]AAAAGCCTAAGTTAA | 93664 |
rs34458584 | snp | A/T | 0.0368353 | 0.130617 | intron-variant | CADPS2 | GRCh38.p7 | 7:122620265 | CTATGAATTAAAGTG[A/T]CACATTGTTACTATT | 93664 |
rs34464177 | in-del | -/A | 0.375 | 0.216506 | intron-variant | CADPS2 | GRCh38.p7 | 7:122879254 | GTGATACTCTGCCTC[-/A]AAAAAAAAAAAAAAA | 93664 |
rs34467456 | in-del | -/A | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122547172 | TACTCTACCCACAAG[-/A]AAATGTTGCTAAAAC | 93664 |
rs34472895 | in-del | -/A | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122827633 | CTCAAAAAAAAAAAA[-/A]GAAATGAAAAGAAAA | 93664 |
rs34474462 | snp | A/G | 0.298398 | 0.245271 | intron-variant | CADPS2 | GRCh38.p7 | 7:122776095 | CCAACTATATGGTTT[A/G]GCTGTGTCCCCACCC | 93664 |
rs34489409 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122878262 | AACTCCGTCTCAAGA[-/A]AAAAAAAAAAAAAAA | 93664 |
rs34500152 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122828866 | ATGGGTCAAGAAATG[-/C]TAGGTCAGGGTGGAC | 93664 |
rs34506571 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122800992 | CGAGACTCTGCCTCA[-/A]AAAAAAAAAAAAAAA | 93664 |
rs34508926 | in-del | -/T | 0.450461 | 0.149384 | intron-variant | CADPS2 | GRCh38.p7 | 7:122668245 | AATTGGAAAATTCCA[-/T]TTTTTTTTACTGGGG | 93664 |
rs34509722 | in-del | -/AT | 0.0352501 | 0.127994 | intron-variant | CADPS2 | GRCh38.p7 | 7:122578213 | TGGTAATGTGTGCAC[-/AT]ATATATATACCCACA | 93664 |
rs34509989 | snp | A/G | 0.299411 | 0.245069 | intron-variant | CADPS2 | GRCh38.p7 | 7:122833688 | GACATGAGCCACCAC[A/G]CCTGGCCTTTATGTT | 93664 |
rs34512351 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122473957 | TTCCCCTGCCACTTA[A/G]GTTGTCCTTCTAAGA | 93664 |
rs34518039 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122430713 | ACAGCTGCTTTCTAG[-/A]AAATGTCCAGTTTTC | 93664 |
rs34527853 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122506727 | CTGCTAGAGTTATTT[-/A]AAAAAAAAAAAAAAA | 93664 |
rs34533065 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122603209 | TAACTCTCAAATCTT[-/A]AAAAAAAGATTATAA | 93664 |
rs34544622 | in-del | -/A | 0.424814 | 0.178718 | intron-variant | CADPS2 | GRCh38.p7 | 7:122660606 | TTAAAAAAAAAAAAA[-/A]GAAAACTTGGGCCAA | 93664 |
rs34549745 | in-del | -/A | 0.260504 | 0.249779 | intron-variant | CADPS2 | GRCh38.p7 | 7:122611319 | TGGGCTAAGAAAAAA[-/A]GAAAGGCTATTCAAA | 93664 |
rs34563576 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122633874 | TTTCTTCAATACCTA[-/G]CCTGTTGAAGGTTTT | 93664 |
rs34565849 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | CADPS2 | GRCh38.p7 | 7:122418826 | CCCATATATTTTAGC[A/G]CTAACTACATTGCCA | 93664 |
rs34577854 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122805582 | TTATCAGCTTACAGC[C/T]TAAGTTGTGGTCCTT | 93664 |
rs34581484 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122625414 | ATCAAACATGAATTT[-/A]AAATGTTGCTATCAA | 93664 |
rs34581969 | in-del | -/A | | | frameshift-variant | CADPS2 | GRCh38.p7 | 7:122388707 | GTGCATCAAGCTTCC[-/A]AAAAAGGTCTTCTGA | 93664 |
rs34582081 | snp | A/G | 0.291235 | 0.246576 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817747 | TCCTTCACTCTTAGC[A/G]GCAAGTCCTGCTTTT | 93664 |
rs34582432 | in-del | -/A/AA/AAA/AAAA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122659310 | GGAAATGCTAGACAT[-/A/AA/AAA/AAAA]AAAAAAAAAAAAAAA | 93664 |
rs34583437 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122714121 | CAAATGTTTGTATAA[-/T]TCCACTTAAACAACT | 93664 |
rs34583891 | in-del | -/G | 0.0429648 | 0.14013 | intron-variant | CADPS2 | GRCh38.p7 | 7:122515937 | TTTAAAAATATATTT[-/G]GAAAAAAAACATGCA | 93664 |
rs34584173 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122493197 | AACTATAAATCAACA[-/G]GGGAAAACTCAGAAC | 93664 |
rs34608490 | in-del | -/A | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122549621 | GTGAGACTCTGTCTT[-/A]AAAAAAAAAAGATTA | 93664 |
rs34611389 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122681591 | TCTCGTGAAGCCCGC[-/A]AGGACCGAACACCCC | 93664 |
rs34612573 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122497351 | TCTATTATCTTATCT[-/C]TGCCCTTTGTATTTG | 93664 |
rs34614200 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122540082 | ATTTATTTTAGCTGC[A/G]TATTTGAGATTTAGT | 93664 |
rs34621721 | snp | A/T | 0.0577344 | 0.159793 | intron-variant | CADPS2 | GRCh38.p7 | 7:122492206 | AATAAATAAATTAAT[A/T]AATTAATTAAATTAA | 93664 |
rs34627169 | snp | A/C | 0.311123 | 0.242413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122814650 | ACAACAGCAGAGTTG[A/C]ACTGTCAAGACAGAG | 93664 |
rs34644562 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122634026 | CAACCTTGCATCCCA[-/G]GAATACTGCTTGATT | 93664 |
rs34648595 | snp | C/T | 0.311859 | 0.242226 | intron-variant | CADPS2 | GRCh38.p7 | 7:122809124 | TTTTCTGTATATACA[C/T]TGTATAAATATTGTT | 93664 |
rs34655911 | in-del | -/G | 0.454302 | 0.144085 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122538674 | TTGGGTAAGGAGATA[-/G]GAAAGTACACTGTAA | 93664 |
rs34666095 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122399585 | TTGAGTTAATGTCCC[A/C]CAATACTTGCCCCAT | 93664 |
rs34671566 | in-del | -/GT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122410729 | TAATTACAAATATGT[-/GT]TGACTACCGCAATCA | 93664 |
rs34676461 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122417160 | ATTTGGAGGAGACAC[-/T]TTTCATTTGCTCTGT | 93664 |
rs34698048 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122450405 | TATGTTAGCATATTT[-/A]CTGTTTTTAATTATT | 93664 |
rs34705183 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122845691 | AGGTTCACATGCACA[-/G]GGGGAGAGTCTTCAA | 93664 |
rs34731459 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | CADPS2 | GRCh38.p7 | 7:122632730 | CAATTTTTGTTTTCA[C/T]TGTAATTGCTTTTGT | 93664 |
rs34735700 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122638322 | GAGGGAGGGCGTCCT[-/C]CCCCACCCCCTGCTT | 93664 |
rs34735967 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122726718 | CTCTTAAAAACTTTT[-/A]AAAAAGAACATAAAA | 93664 |
rs34754444 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122678202 | AAAAAGAAAATACAA[-/G]GGACTTCAAAGTCCA | 93664 |
rs34758804 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122491279 | TTCCATGCATACATA[A/C]ATGGCAGGAAAAGTG | 93664 |
rs34758968 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122727341 | ACACTGAAGTAAATT[-/G]GCATGTGCTTCTTTC | 93664 |
rs34761338 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | CADPS2 | GRCh38.p7 | 7:122375338 | AAAAAGTAAACAATG[C/T]TAACTTTTTTAAGTA | 93664 |
rs34763394 | in-del | -/CT | 0.322959 | 0.239117 | intron-variant | CADPS2 | GRCh38.p7 | 7:122864471 | GGCAACAAAGTGAAA[-/CT]CTGTCTCAAAAAACA | 93664 |
rs34775297 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122734828 | CATAATGAGCATCAC[-/A]AAATCTTAACACCAT | 93664 |
rs34788333 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122365486 | TACCTTCCACCTGGC[-/T]TTTTAATTGCATAAA | 93664 |
rs34791066 | in-del | -/T | 0.185155 | 0.241444 | intron-variant | CADPS2 | GRCh38.p7 | 7:122429881 | CCACAAACTGTGCAG[-/T]TTTTTTTTTTAATAA | 93664 |
rs34823105 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122795744 | ATGACATACCCACCA[-/G]CAAACATCATACTGA | 93664 |
rs34824430 | snp | C/G | 0.324145 | 0.238752 | intron-variant | CADPS2 | GRCh38.p7 | 7:122871815 | TGTGACATGGACCAT[C/G]CTAGTTTTCTTCTAA | 93664 |
rs34849650 | in-del | -/A/AA | 0.4862 | 0.0819127 | intron-variant | CADPS2 | GRCh38.p7 | 7:122580452 | AAAAAAAAAAAAAAA[-/A/AA]CCCATTAAAAAATTC | 93664 |
rs34867446 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122469555 | TGTGAGATAGTGGGG[-/A]AAAAACTACTAAAAT | 93664 |
rs34872485 | in-del | -/A | 0.424503 | 0.179021 | intron-variant | CADPS2 | GRCh38.p7 | 7:122809580 | GAGAGACACTGTCTC[-/A]AAAAAAAAAAAAAAA | 93664 |
rs34875458 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122489960 | TACTAATATGAACTA[-/T]TTTTCATTTAATTAG | 93664 |
rs34877809 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122405236 | GTTTACTGTTATACA[-/T]TTTGTCTTAAGATAA | 93664 |
rs34893488 | snp | A/G | 0.312104 | 0.242163 | intron-variant | CADPS2 | GRCh38.p7 | 7:122809061 | TGTTACCAAAACAAG[A/G]ATGTTTGCCTTTAGT | 93664 |
rs34898334 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122641360 | CCTGTTCATTACACA[-/G]GGGATTACTGTTTCC | 93664 |
rs34903434 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122412981 | ATCACTCCTGCAATT[-/C]CTACTTAAATTGCAA | 93664 |
rs34908983 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122761848 | AAAAAAAAAAAAAAA[-/A]TTAGCCGGGTGTGGT | 93664 |
rs34910927 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122749961 | TTCACCTGTGAGGTT[-/A]AAAAAAAAAAAAAAA | 93664 |
rs34912559 | in-del | -/A | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122553216 | ATACAAGTCTGAATT[-/A]CCTGACTAGCCAGTT | 93664 |
rs34921799 | in-del | -/AC | 0.48546 | 0.0840147 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122550764 | ATCTTCATGCTACAG[-/AC]ACACACACACACACA | 93664 |
rs34924150 | in-del | -/G | 0.306679 | 0.24349 | intron-variant | CADPS2 | GRCh38.p7 | 7:122787677 | CTAGTGCAATGCAAA[-/G]CACATTGTAGCCTCC | 93664 |
rs34926002 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122425268 | TTACATTCGTGAGCC[A/C]CCATACTCAGCCATA | 93664 |
rs34927994 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | CADPS2 | GRCh38.p7 | 7:122662620 | ACCTCACTATCTGCC[C/T]GCCTCAGCCTCCCAA | 93664 |
rs34929427 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122679675 | CTCAGGGGGCATCAC[-/G]GGAACCTGCCGACAT | 93664 |
rs34938240 | snp | A/C | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122818519 | GCCTGTCCCCTCAGT[A/C]CCAACCCCAAGCATC | 93664 |
rs34938284 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122830397 | GCTAAAAAAAAAAAA[-/A]TCAAAGGATGCAAAT | 93664 |
rs34950493 | snp | C/T | 0.0788843 | 0.182262 | intron-variant | CADPS2 | GRCh38.p7 | 7:122705200 | AAGTATCATGACAAA[C/T]TGCATATATTTTATC | 93664 |
rs34955892 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | CADPS2 | GRCh38.p7 | 7:122644014 | GGCGGAGATTGCAGT[A/G]AGCCAAGATGGCGCC | 93664 |
rs34959847 | snp | A/G | 0.259951 | 0.249802 | intron-variant | CADPS2 | GRCh38.p7 | 7:122807651 | AGAGGCTGGAAGTCC[A/G]AGATCAAAGTGTTGG | 93664 |
rs34977196 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122479955 | CTACTATTCATATTG[G/T]ATTATGTGACACACA | 93664 |
rs34986947 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122649927 | TTTTTTTTTTTTTTT[G/T]GAGAGAGTCTCACTT | 93664 |
rs34989009 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122339284 | TCACTTTTATCCATG[-/T]TTTTGTTGATTTCAA | 93664 |
rs34996363 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122823873 | TAAGCATCAGACTCA[-/G]GGGGTTGTGCAGGAG | 93664 |
rs35005680 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122359521 | TAAGAACATGAATAA[-/T]TTTTGGTGTCACAGT | 93664 |
rs35010584 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122814069 | TGAGTCTGAGAAAAA[-/T]TTTCAGTAACTTGGC | 93664 |
rs35011683 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122602713 | TCACAGAAACAACTT[-/C]CCTGTATTCTCTTCT | 93664 |
rs35015771 | in-del | -/A | 0.367881 | 0.220463 | intron-variant | CADPS2 | GRCh38.p7 | 7:122731675 | AAAGGTGAAGAGGGG[-/A]AAAAAAAACCCTTCA | 93664 |
rs35021210 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122654344 | GTCAGAAGATGCCAT[-/C]CTAGGGTTTTCATAG | 93664 |
rs35033334 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122411667 | GATTAGTTTGCAATT[-/C]CTGTACTTTGTTGAT | 93664 |
rs35036249 | snp | C/G | 0.330714 | 0.236612 | intron-variant | CADPS2 | GRCh38.p7 | 7:122758265 | AAGAAATGAATTTCT[C/G]ACTCCTTTTGGTATT | 93664 |
rs35044104 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122484780 | TATCCAGAACACACA[-/G]GGGAAACTTCATTTT | 93664 |
rs35047637 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122611969 | AATCCACATGATCAT[-/G]CTCAATAGATGTAGG | 93664 |
rs35050756 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122410726 | CAGTAATTACAAATA[-/T]GTGTTGACTACCGCA | 93664 |
rs35053952 | in-del | -/A/AA | 0.499999 | 0.000798721 | intron-variant | CADPS2 | GRCh38.p7 | 7:122642279 | GTGAGACTCCATCTC[-/A/AA]AAAAAAAAAAAAAAA | 93664 |
rs35065500 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122470551 | CTAGGCTGGAGTGCA[A/G]TGGCATGATCTTGGC | 93664 |
rs35074105 | in-del | -/C | 0.202035 | 0.245356 | intron-variant | CADPS2 | GRCh38.p7 | 7:122679138 | CTTAAAGTCTGGCTG[-/C]CTGTGGGCCGGGCAG | 93664 |
rs35090045 | snp | C/G | 0.0448719 | 0.142907 | intron-variant | CADPS2 | GRCh38.p7 | 7:122418812 | CTTCAATGGACCATC[C/G]CATATATTTTAGCAC | 93664 |
rs35095733 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122461881 | TTAAAGGTGTGAGCC[-/A]CCTCGCCTGGCCTGC | 93664 |
rs35099606 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122365371 | TACAGTTCCTACAGG[-/A]AAAGTTTTCTTTGTA | 93664 |
rs35101326 | in-del | -/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122847598 | TAGATTTTTTTTTTT[-/T]CTTGTCATCATTAAC | 93664 |
rs35103663 | in-del | -/TCA | 0.339203 | 0.233544 | intron-variant | CADPS2 | GRCh38.p7 | 7:122761401 | TGCTCACAAAGTAAT[-/TCA]GCCAGATCACAAATT | 93664 |
rs35112783 | in-del | -/A | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122759002 | GGAAAAAAAAAAAAA[-/A]TTAAAGGTCCTTAAA | 93664 |
rs35127611 | in-del | -/TT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122625066 | TTATTTTTTTTTTTT[-/TT]GAGACAGAGTTTCGC | 93664 |
rs35127684 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | CADPS2 | GRCh38.p7 | 7:122643321 | AATCAAAAATTATTT[A/G]CAATAAAGATAGAGC | 93664 |
rs35131640 | snp | C/T | 0.242201 | 0.249878 | intron-variant | CADPS2 | GRCh38.p7 | 7:122616840 | TTTGTTAGATTCTTA[C/T]ACAAAATGAAACCAG | 93664 |
rs35132220 | snp | A/G | 0.163236 | 0.234461 | intron-variant, nc-transcript-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122531143 | GCAAGCTGTACTGGT[A/G]GTTTATTATATTCTT | 93664 |
rs35145747 | snp | C/T | 0.331642 | 0.236293 | intron-variant | CADPS2 | GRCh38.p7 | 7:122833513 | CAAGTGCCCCCGTCC[C/T]CCCACCACACCCAGC | 93664 |
rs35147547 | snp | C/T | 0.255224 | 0.249945 | intron-variant | CADPS2 | GRCh38.p7 | 7:122579793 | AAGCACATGACTGAA[C/T]GAGCAGTAACACAGC | 93664 |
rs35148799 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122417588 | TGAACATTTCAACAT[-/C]CTCAAAGAAGCATGA | 93664 |
rs35150473 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122786935 | ATGAGAACAGGTCAT[-/G]GGATGTAGCATTTCT | 93664 |
rs35168749 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | CADPS2 | GRCh38.p7 | 7:122406438 | GTGTGAAGAAGTTCC[C/T]TGGAGAGTCAGAGCA | 93664 |
rs35176496 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122628458 | AGAAATAGAGAGGGA[-/G]GACTATCCATCAAAT | 93664 |
rs35186619 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | CADPS2 | GRCh38.p7 | 7:122662722 | AACTGAAGAGAAAAT[A/G]TAATATTCACTCTGT | 93664 |
rs35202510 | in-del | -/GTGT | 0.457271 | 0.139781 | intron-variant | CADPS2 | GRCh38.p7 | 7:122427121 | ATTACATAAATGCCG[-/GTGT]GTGTGTGTGTGTGTG | 93664 |
rs35204401 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122607122 | GTTGTAGACAGATTA[G/T]ACGATCAGGAAAAGC | 93664 |
rs35206399 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122863464 | TGCCCAATCACAGAG[-/A]AAAATTCAAAAACAC | 93664 |
rs35227196 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122731970 | ACTTATAATACTTAA[-/G]GACATCTTATTAAAA | 93664 |
rs35243595 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122470164 | AAAGTTATTCTACAA[-/T]TTTTTTTGACTGATT | 93664 |
rs35248065 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122500231 | ACCATTCTAACCTTG[G/T]TTGTCATTTTTTTGT | 93664 |
rs35248314 | in-del | -/A | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122535699 | ATTTGGATTTTTGAT[-/A]AATAACTCATGCAAA | 93664 |
rs35248522 | snp | G/T | 0.167158 | 0.235875 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122543094 | TAATCTGTGAATTCT[G/T]GTATAAGGATATTTT | 93664 |
rs35251970 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122664039 | CTCCAGAACTGTAAG[-/C]AAATAAATGACCATT | 93664 |
rs35252845 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122689811 | CCCACAGTGACTTTA[-/C]CCCCAGTGCTGCTCT | 93664 |
rs35257634 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122467826 | GTCTCTGAAAGCCTC[-/T]TTTTCTCCTTCCTGT | 93664 |
rs35258384 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122332410 | TTTTTTTTTTTTTTT[-/T]CAATCAGAACAGAGA | 93664 |
rs35276739 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122339206 | CAAATAATATGACTG[-/A]AAAAGTACATTATCA | 93664 |
rs35278478 | in-del | -/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122540643 | GCATATTATTAAGGT[-/G]CCCACAATTCTTCAT | 93664 |
rs35284011 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122789570 | GGACACAAATACAAA[-/T]TTTTCCCCCTACCAC | 93664 |
rs35285118 | snp | C/T | 0.336474 | 0.234568 | intron-variant | CADPS2 | GRCh38.p7 | 7:122330453 | GTCTAAACACTAAAA[C/T]GCAAATGTTATATTA | 93664 |
rs35286197 | snp | A/T | 0.0607341 | 0.163335 | intron-variant | CADPS2 | GRCh38.p7 | 7:122707942 | AACTATAATTCTTAT[A/T]TCTATATATATATTT | 93664 |
rs35287423 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122796574 | GCACACCTACAACTA[-/T]TCAGATCTTCAACAA | 93664 |
rs35290526 | in-del | -/A/AA/AAA | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122726773 | AAAAAAAAAAAAAAA[-/A/AA/AAA]CTATCCACATATAAG | 93664 |
rs35296798 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122501898 | AAAAAAAAAAAAAAA[A/G]GGAAAAAAAAAGTCA | 93664 |
rs35320917 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122671449 | CACAGAGGAAAGGCT[-/G]GGACTGTGGTGGCTC | 93664 |
rs35322616 | in-del | -/C | | | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122704056 | TGTATAGGTTATCTT[-/C]CTATGTGCTCAGCAT | 93664 |
rs35325666 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122720725 | TCCTGTAATATTCCT[-/A]AAAGTGAATCACCTA | 93664 |
rs35331526 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | CADPS2 | GRCh38.p7 | 7:122618839 | ATGCACTGCACCATC[A/G]TCACTTAACACGATT | 93664 |
rs35335008 | snp | C/G | 0.330714 | 0.236612 | intron-variant | CADPS2 | GRCh38.p7 | 7:122766257 | CCACTCCCTACCACA[C/G]AACACTGCAACTTTG | 93664 |
rs35337102 | snp | A/G | 0.118933 | 0.212888 | intron-variant | CADPS2 | GRCh38.p7 | 7:122496317 | CAGGTGTGCGCTACC[A/G]TATCTGGCTAACTGT | 93664 |
rs35343265 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122357875 | TATTTATACATTGAC[-/G]GTACTACAGGACAAT | 93664 |
rs35344551 | in-del | -/AT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122428453 | CATATATATACACAC[-/AT]ATATATATATATATA | 93664 |
rs35345335 | snp | A/G | 0.259951 | 0.249802 | intron-variant | CADPS2 | GRCh38.p7 | 7:122611839 | AAAACCAAATCCAGT[A/G]ACAAATTTTAAAAAT | 93664 |
rs35346695 | in-del | -/A | 0.483923 | 0.0882034 | intron-variant | CADPS2 | GRCh38.p7 | 7:122710082 | ACCTTCTGCCAACCC[-/A]AAAAAAAAAAAAATC | 93664 |
rs35347547 | in-del | -/C | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122534863 | AAGCAAATACAGTTT[-/C]CTGAGTATGTGGCAA | 93664 |
rs35349024 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122446606 | GCCTTTCCTGTGGTT[-/G]CTTTGCCAGACTTTG | 93664 |
rs35352825 | in-del | -/A | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122540885 | CAATTGATTTTATAG[-/A]AAATGTAAGTTATAG | 93664 |
rs35352953 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122481162 | TTTCTTTCTTCATTC[-/T]TTTTTTTTTTTTTTT | 93664 |
rs35353379 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122375975 | TGGCCAACAGGTATA[-/C]CGAAAAGGAGCTTAA | 93664 |
rs35361124 | in-del | -/A | 0.4983 | 0.0291038 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122538147 | TATACAAAGTTCAGT[-/A]AAAAAAAAAAGAGAA | 93664 |
rs35364064 | in-del | -/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122541199 | GGTATTATGAGATGA[-/T]TTTTTTTTTTTTTTT | 93664 |
rs35370048 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122757908 | TATTCACATAGCACA[-/G]GGGAAAAAAAAACTA | 93664 |
rs35372605 | snp | C/G | 0.181978 | 0.240568 | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122704947 | AAGAAATTATGTGGT[C/G]CAAAATATCAATAGT | 93664 |
rs35380309 | snp | A/G | 0.167158 | 0.235875 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122560412 | TACAAACCAGAGAAT[A/G]AAAATCAAATTTTCA | 93664 |
rs35387381 | snp | C/T | 0.348354 | 0.22984 | intron-variant | CADPS2 | GRCh38.p7 | 7:122796912 | ACAGCAAACTATCAA[C/T]AGAGTGAACAGACAA | 93664 |
rs35396872 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122618445 | AATAACTGAACTATA[-/T]TGTTAGTTGGTAAGT | 93664 |
rs35401073 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122793309 | TGAATCTGGGTGCTT[-/C]CCATGCTGGGTGCAT | 93664 |
rs35414927 | in-del | -/A | 0.334182 | 0.235401 | intron-variant | CADPS2 | GRCh38.p7 | 7:122668403 | AGACAAAGTATGGTT[-/A]AAAAAAAAAAAAAAA | 93664 |
rs35415030 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122795742 | TCTATGACATACCCA[-/C]CACAAACATCATACT | 93664 |
rs35444763 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122602102 | TAGGTGGTTTGAGTT[-/A]AAAGTTTCCGTTAAA | 93664 |
rs35449360 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122601982 | TCAGCTTGCCATTAA[-/C]CCTTACTAAATAACT | 93664 |
rs35449906 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122338859 | CAAACTCCTGGACTT[-/G]GGATGATCCTCTCGC | 93664 |
rs35451971 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122417242 | CGGTGCTCATTCATT[-/A]AAATATTCATTATAT | 93664 |
rs35459522 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122876569 | AGTCTCACTGTGTAG[-/C]CTAGGCTGTTCTCCA | 93664 |
rs35462947 | snp | A/C | 0.162581 | 0.234218 | intron-variant | CADPS2 | GRCh38.p7 | 7:122612054 | AGGAATAGAAATGAA[A/C]TTCCTTAAACTGCTA | 93664 |
rs35464136 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122859466 | TCATTTTAGAACCTT[-/G]GGTCATTTAGAACCT | 93664 |
rs35466286 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122462579 | CTAATTAAAGGACAG[-/T]AAATAGTCATATTGA | 93664 |
rs35468775 | in-del | -/AT/TA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122725338 | GAAAACATCTCTTTT[-/AT/TA]ATATATATATGTATA | 93664 |
rs35474147 | snp | C/T | 0.338976 | 0.23363 | intron-variant | CADPS2 | GRCh38.p7 | 7:122763341 | GCAAAGGGGATAGTG[C/T]GATGAGAGTGCTGAA | 93664 |
rs35485863 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122329227 | TCTTGAATTAACAAA[-/C]CCAAAGCAATGAAAG | 93664 |
rs35486160 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122754928 | AAAACATATTCTTAA[-/G]GAACATAGGAGAACT | 93664 |
rs35488792 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122321224 | AGGCTGGAGTACAGC[-/G]GGTGTGATCATTGCT | 93664 |
rs35489038 | in-del | -/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122597925 | ACATTTTTTTTTTTT[-/T]GAAACAAGAATAACA | 93664 |
rs35494780 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122774727 | ATTTCTAGTTTAAAT[-/G]GGATGTAGGAAAGCA | 93664 |
rs35499997 | snp | A/T | 0.0618563 | 0.164627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122492215 | ATTAATTAATTAATT[A/T]AATTAAATTAAAATA | 93664 |
rs35500887 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122500383 | AAATGTACTATTTTT[-/G]GAAAGTATAAGCCAC | 93664 |
rs35500917 | snp | C/T | 0.420892 | 0.182472 | intron-variant | CADPS2 | GRCh38.p7 | 7:122489180 | TAAAGAAATAAAAAG[C/T]TCATGGTTCACATTT | 93664 |
rs35508723 | snp | A/G | 0.312104 | 0.242163 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817994 | TTATTTCCATGCCCC[A/G]ACCCCTTATTTCTGC | 93664 |
rs35510489 | in-del | -/CA | 0.49917 | 0.0203505 | intron-variant | CADPS2 | GRCh38.p7 | 7:122747840 | GTCATTGTGCCTTTG[-/CA]CACAGTTTGCTTCCT | 93664 |
rs35514146 | in-del | -/T/TTTT | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122408180 | AAGGATATACTGTTA[-/T/TTTT]TTTTTTTTTTTTTAC | 93664 |
rs35521156 | snp | C/T | 0.332799 | 0.23589 | intron-variant | CADPS2 | GRCh38.p7 | 7:122819812 | TCCCCCCACCTTAAT[C/T]CACAAGTATAAGATA | 93664 |
rs35528908 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122365483 | ATATACCTTCCACCT[-/G]GGCTTTTAATTGCAT | 93664 |
rs35541004 | snp | A/T | 0.259397 | 0.249823 | intron-variant | CADPS2 | GRCh38.p7 | 7:122815624 | AATGAAATACAAAAA[A/T]AATTCAAAATATATT | 93664 |
rs35546096 | snp | C/T | 0.206419 | 0.246172 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122540003 | ATTTTATATTTAATA[C/T]ATTTACTCTTTTGTG | 93664 |
rs35558114 | in-del | -/TT/TTT/TTTT | 0.475789 | 0.107327 | intron-variant | CADPS2 | GRCh38.p7 | 7:122666360 | TTTTTTTTTTTTTTT[-/TT/TTT/TTTT]GAGATGGAGTCTTGC | 93664 |
rs35560374 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122487094 | ATTTCACTGCAACCT[-/C]CCACCCCTCGGGTTC | 93664 |
rs35566130 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122385473 | GATGAGAATTGTCAG[-/C]CCCAGGAAGAGTCAC | 93664 |
rs35569543 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122679222 | TTCTTTCCCCAGTAA[-/G]GGAATATTAATAATT | 93664 |
rs35572612 | in-del | -/T | 0.31014 | 0.242659 | intron-variant | CADPS2 | GRCh38.p7 | 7:122773652 | TGTTTACACACATCC[-/T]TTATGTTGTGCAGTG | 93664 |
rs35574664 | snp | A/T | 0.0733688 | 0.176922 | intron-variant | CADPS2 | GRCh38.p7 | 7:122501340 | AGATATTACATTTGG[A/T]AATTTAAAACTATGA | 93664 |
rs35577980 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122642468 | AGGGAGAACTGGAAG[C/G]CTGTGCTGGCAGCCA | 93664 |
rs35592866 | in-del | -/C | | | downstream-variant-500B | CADPS2 | GRCh38.p7 | 7:122318262 | GGCCGCAAATACTTT[-/C]CCCCTGCAGCATCTG | 93664 |
rs35598306 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122581580 | TGTAGCTATTGAAAT[-/C]CTATTACTTTATTAA | 93664 |
rs35598681 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122431963 | CAAAGAAGTAAATTA[G/T]TTGATACATCACATA | 93664 |
rs35600638 | in-del | -/A/AA | 0.40086 | 0.199352 | intron-variant | CADPS2 | GRCh38.p7 | 7:122618043 | CAAAAAAAAAAAAAA[-/A/AA]TCAACTATATTCATG | 93664 |
rs35604970 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | CADPS2 | GRCh38.p7 | 7:122614460 | AAAATCCTAAATCCT[A/G]TAAGATATTTAGAAT | 93664 |
rs35614548 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122867006 | TTCTATTCCACCACA[-/G]GGACTTTTTATTCTT | 93664 |
rs35620625 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122389965 | TATGAGCTAGCTTAG[-/A]AAAAAAGGCACCTCT | 93664 |
rs35625301 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122384303 | TTTATCCCAGCGATG[A/C]CAATATAACACATTT | 93664 |
rs35628062 | snp | C/G | 0.0460142 | 0.144533 | intron-variant | CADPS2 | GRCh38.p7 | 7:122647106 | ATCAGTTTACCATGG[C/G]TTTAAGTGACACAGT | 93664 |
rs35635790 | in-del | -/A/CA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122326075 | AAAAAAAAAAAAAAA[-/A/CA]TCTACAACTTAAACA | 93664 |
rs35636140 | snp | C/T | 0.165527 | 0.235296 | intron-variant | CADPS2 | GRCh38.p7 | 7:122408087 | TTCTGTGAATAGAAA[C/T]ATTAAAACATTTGGT | 93664 |
rs35641731 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122412619 | AATTACTGCCAAACA[-/C]ACCTTCTTGCCCACG | 93664 |
rs35644056 | in-del | -/GTA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122764595 | AATGAAGCAAAATAA[-/GTA]GTCAGGGTATAGCAA | 93664 |
rs35653351 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122670348 | TTGGGAGGCCAAAGT[-/G]GGGAGGATCACTTGA | 93664 |
rs35654513 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122321982 | AGTTATTATGACTAA[-/G]GGTAGTACTCTCTTA | 93664 |
rs35656094 | in-del | -/T | | | intron-variant, upstream-variant-2KB | CADPS2, LOC105375481 | GRCh38.p7 | 7:122528784 | TTCAAGTTTTGGATA[-/T]TTTTTTGTTAAAACT | 93664 |
rs35656607 | in-del | -/A | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122416309 | ACAAAAAAAAAAAAA[-/A]CAGTTCACCAGATTG | 93664 |
rs35658742 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122654777 | AGTCTTATTATTTAA[-/G]GAAATACAGTTTGTA | 93664 |
rs35669479 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122793952 | AATGTTGAGTATTGA[-/C]CCCCCAATCTCTTCT | 93664 |
rs35693025 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122486177 | AGGAGTAATTTCAAC[-/T]TTTCAAGTCTTATTA | 93664 |
rs35703572 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122607921 | TGCCTTTGGTTCATT[-/A]AAAATAGGCACAGTT | 93664 |
rs35710414 | in-del | -/T | | | intron-variant, utr-variant-5-prime | CADPS2 | GRCh38.p7 | 7:122885923 | TCGCAGAAGGACGGG[-/T]AGGCGTCCCAGAGCT | 93664 |
rs35710523 | snp | G/T | 0.046775 | 0.145601 | intron-variant | CADPS2 | GRCh38.p7 | 7:122455923 | GGCCAGGCTGGTCTC[G/T]AACTCCTGGCCTCAG | 93664 |
rs35715868 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122876972 | AAAGGTAAAATGTTT[-/C]CTCAGTTAACACCTT | 93664 |
rs35720265 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122830068 | TCACTGTTTCAAGGA[-/G]GAGAAAACTTTGGAC | 93664 |
rs35722950 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122637283 | CTGCAGCCTCGACCT[-/C]CCCTGACTCAAGTGA | 93664 |
rs35723351 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122869615 | TAAAGGAGAAGATCA[-/C]TAAGGAGCAACACAA | 93664 |
rs35724404 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122796528 | GATACATAAACCAAT[-/G]GGAACAGCATACAGA | 93664 |
rs35730008 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122461436 | CATATATGTCCCAAT[-/C]CACAATAAATTAAAA | 93664 |
rs35739381 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122379342 | TTTTCACTTTGATTT[-/A]AAAAGGTGAATAAAT | 93664 |
rs35751114 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122805486 | TTGTTTACTTCCCTT[-/A]ATATTTTAGATAGTT | 93664 |
rs35759423 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122343208 | AAAAATGTGCAATTT[A/T]AAAATATTAGAATGT | 93664 |
rs35760934 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | CADPS2 | GRCh38.p7 | 7:122418789 | GTTGATAAAGTTAGG[C/T]AATGGGTCTTCAATG | 93664 |
rs35778660 | snp | G/T | 0.260504 | 0.249779 | intron-variant | CADPS2 | GRCh38.p7 | 7:122612504 | ATAAAACTTTTACTT[G/T]GAAAACTACAAGACA | 93664 |
rs35781446 | in-del | -/ATC | 0.0766824 | 0.180169 | intron-variant | CADPS2 | GRCh38.p7 | 7:122514252 | ATTTTTCAATATTTT[-/ATC]ATAATCCTTTATTCT | 93664 |
rs35781696 | in-del | -/T | 0.422158 | 0.181278 | intron-variant | CADPS2 | GRCh38.p7 | 7:122882617 | ACCACCAAGGAACCC[-/T]TTTTTTTTTTTTTTT | 93664 |
rs35786663 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122577335 | CCTGTGTACCCCTTT[A/C]TGGCTGACAACCCAC | 93664 |
rs35788531 | in-del | -/A | 0.322245 | 0.239334 | intron-variant | CADPS2 | GRCh38.p7 | 7:122670870 | GTGAAACCCTGTTTC[-/A]AAAAAAAAAAAAAAA | 93664 |
rs35805017 | in-del | -/T | 0.0733688 | 0.176922 | intron-variant | CADPS2 | GRCh38.p7 | 7:122501343 | TATTACATTTGGAAA[-/T]TTAAAACTATGATTT | 93664 |
rs35808900 | snp | C/T | 0.289424 | 0.246872 | intron-variant | CADPS2 | GRCh38.p7 | 7:122842441 | ACCCTGCCCTGAAAT[C/T]CAGTAACAGGACCTT | 93664 |
rs35813925 | in-del | -/T | 0.375 | 0.216506 | intron-variant | CADPS2 | GRCh38.p7 | 7:122463151 | TAAAGAATACATATA[-/T]TTTTTTTTAAGTGAC | 93664 |
rs35816048 | in-del | -/AAA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122422808 | AAAAAAAAAAAAAAA[-/AAA]TAGCCTGGCGTGGTG | 93664 |
rs35817302 | snp | C/T | 0.331179 | 0.236453 | intron-variant | CADPS2 | GRCh38.p7 | 7:122807951 | GACTTCAACAAATGA[C/T]GTAGATATAAAGTTT | 93664 |
rs35825527 | snp | C/T | 0.225893 | 0.248835 | intron-variant | CADPS2 | GRCh38.p7 | 7:122708623 | TTAGCCATACCTTAA[C/T]ACAAAGATAAATGAG | 93664 |
rs35826487 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122351665 | CATTACTGCAGAGTT[-/A]CTTGTCCTGGATCAG | 93664 |
rs35826922 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122458408 | GTATTACTTGGATGG[G/T]CATATATTACACACT | 93664 |
rs35830455 | in-del | -/A | 0.309648 | 0.24278 | intron-variant | CADPS2 | GRCh38.p7 | 7:122848909 | GAAGACTTTACTAAG[-/A]AAAAAAAATGCTCCT | 93664 |
rs35839200 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122663775 | TTAAAATGTGTAGGA[-/G]GACACAGTATACAGT | 93664 |
rs35850048 | in-del | -/T | 0.137527 | 0.223271 | intron-variant | CADPS2 | GRCh38.p7 | 7:122363049 | AATCCACCCACAAAA[-/T]TGCGAATTGCTCACA | 93664 |
rs35850705 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122355287 | TTTATTTATTGCTTT[-/A]AAAAACATTCCAGCC | 93664 |
rs35862887 | in-del | -/A | 0.067446 | 0.170804 | intron-variant | CADPS2 | GRCh38.p7 | 7:122684655 | CTGATAAAATACCTC[-/A]AAAAAACCTTTCACT | 93664 |
rs35866765 | snp | A/G | 0.0755793 | 0.179102 | intron-variant | CADPS2 | GRCh38.p7 | 7:122510059 | GTGTTAAAGGTAACA[A/G]ATTATTTTATAATAA | 93664 |
rs35868108 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122689231 | TAACCTCCTGGGACA[-/C]CCCCTTGTAAAGCTG | 93664 |
rs35868467 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122476361 | TATCTTTTTCCTGTG[-/A]AAAAAGTAAAAAAAT | 93664 |
rs35878180 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122349766 | AAAGAGAAAAAAATT[-/C]CCTTGTTAATTATAT | 93664 |
rs35881192 | in-del | -/AG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122527582 | AAGATAATACTGAAT[-/AG]AGAGAGAGAGAGAGA | 93664 |
rs35888537 | in-del | -/TTT | 0.0260105 | 0.111035 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122545547 | TGGGAAGCAACTGAA[-/TTT]TTTTTTTAGTAGAGA | 93664 |
rs35893323 | in-del | -/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122542444 | ATAACTAAGTGCAAG[-/T]TTTGGGAAGGTATTA | 93664 |
rs35914742 | snp | C/T | 0.421051 | 0.182323 | intron-variant | CADPS2 | GRCh38.p7 | 7:122788701 | TGGCTTTAGGCTGAT[C/T]GCACTATGCCAAGAC | 93664 |
rs35916918 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122461736 | GTAGCTGGGACGACA[-/G]GGTGCGTGGCACCAT | 93664 |
rs35918217 | snp | C/T | 0.311369 | 0.242351 | intron-variant | CADPS2 | GRCh38.p7 | 7:122776307 | GCCATGTAAGACATG[C/T]CTTTGCTCTTCCTTC | 93664 |
rs35925737 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122333378 | AATGGGACACATTCC[-/A]AAATCTTCTTTTAAG | 93664 |
rs35926156 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122639720 | TTTACAAAATACTTC[-/A]AAATAAATTATACTA | 93664 |
rs35928306 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122639076 | ATTTTGTGAAACTGG[-/A]AAAGCATACTTCCAA | 93664 |
rs35931003 | snp | A/C | 0.298651 | 0.24522 | intron-variant | CADPS2 | GRCh38.p7 | 7:122776125 | CAAATCTCATATTGA[A/C]TTGTAGCTCCCATAA | 93664 |
rs35936616 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122596079 | GTCACTGCCAGTTAT[-/A]CCTGCTGCTGCTGGT | 93664 |
rs35944196 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122884659 | GTTTGTGTGTGTTTT[-/A]AAAAGTTGGGTAAGA | 93664 |
rs35967022 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | CADPS2 | GRCh38.p7 | 7:122578358 | AAAGCAGGTATGAGT[A/G]TACAATGTTTGAGGA | 93664 |
rs35971020 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122416309 | GACAAAAAAAAAAAA[-/A]CAGTTCACCAGATTG | 93664 |
rs35982750 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122367235 | AGATTTATCTTCTAT[-/A]CTATCCTATTCTTAA | 93664 |
rs35984016 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122464072 | TAAATACCATTCTCT[-/A]AAAAACAAACAAACA | 93664 |
rs35986281 | snp | A/G | 0.114387 | 0.210022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122658629 | TCTCAGCAAACTATC[A/G]CAAGGACAGAAAACC | 93664 |
rs35994164 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122585854 | TATTTGCTATTAAAT[-/A]AAAGGGTACTGGAAA | 93664 |
rs35998200 | snp | A/G | 0.155656 | 0.231515 | intron-variant | CADPS2 | GRCh38.p7 | 7:122518517 | AGTATGAGTCTACCA[A/G]ATAAACATATAGAAA | 93664 |
rs35999525 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122508062 | ACACTACTTGTGTAG[-/C]AAAATTTTATACACA | 93664 |
rs36005353 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122675949 | CCATGCAACAAACCT[-/G]GCACGTTCTGTACAT | 93664 |
rs36019960 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122331499 | AAAAAATTAGTTGGG[C/T]GCTGTGACGTGTGCC | 93664 |
rs36034308 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122603271 | ACAAACACCCAAGCC[-/A]AAAATCTCAGAAGGG | 93664 |
rs36048476 | in-del | -/T | 0.0733688 | 0.176922 | intron-variant | CADPS2 | GRCh38.p7 | 7:122503419 | TGAATGATTTAGTGG[-/T]TTTTATCTTAGAAAC | 93664 |
rs36048741 | in-del | -/A | 0.202035 | 0.245356 | intron-variant | CADPS2 | GRCh38.p7 | 7:122672582 | CTGGCTTGAGGTCAC[-/A]ACACCTCCTGGGAGA | 93664 |
rs36049064 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122643911 | CTTGGGCAACATGGC[-/A]AAAACCCCTCTCTAC | 93664 |
rs36057959 | snp | C/T | 0.266546 | 0.249452 | intron-variant | CADPS2 | GRCh38.p7 | 7:122570583 | AAAGACACATGCACA[C/T]GTATGTTTATTGTGG | 93664 |
rs36072017 | snp | C/T | 0.311123 | 0.242413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122809118 | ATGTGGTTTTCTGTA[C/T]ATACATTGTATAAAT | 93664 |
rs36090524 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122639474 | CAGGATCCTGACTTT[-/G]GGCTACGTAATCACC | 93664 |
rs36093335 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122376940 | ATTAATTTGCATCAT[-/C]CTTTTTAAAAAACAT | 93664 |
rs36096509 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122775975 | TTCAAGTTCAAAAAT[-/T]TTTTTTCTAGAGAAG | 93664 |
rs36106092 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122564725 | ATGCCTACGTTTATC[A/T]CAGCGTTAGTCACAA | 93664 |
rs36106438 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122595161 | TGTGTTATATGAACC[-/A]AAAAAAAAAAAATCC | 93664 |
rs36108447 | snp | A/C | 0.330947 | 0.236533 | intron-variant | CADPS2 | GRCh38.p7 | 7:122770522 | GGTTCCCTGACCCCA[A/C]TCCCCTGAACTCAGT | 93664 |
rs36109949 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122352013 | GCCTGAACTACTCAA[-/G]GGGGACAAGGTAATT | 93664 |
rs36122169 | snp | A/G | 0.306679 | 0.24349 | intron-variant | CADPS2 | GRCh38.p7 | 7:122844094 | AGCCACAGTGAGTCT[A/G]TAGCCTTCTGCTTCC | 93664 |
rs36122976 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122341928 | AACATCATGGACCTG[-/C]CCATAACTTATTTAT | 93664 |
rs36153084 | snp | G/T | 0.5 | 0 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122541847 | CATATGTTTATATAT[G/T]CATATATATTTATAT | 93664 |
rs36154725 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122717991 | ACCACACTCGGCTAA[-/T]TTTTTTTTTTTTTTT | 93664 |
rs36199206 | snp | A/T | 0.330947 | 0.236533 | intron-variant | CADPS2 | GRCh38.p7 | 7:122838898 | CCATCAAGTTACCAA[A/T]GACTTTCTTCACAGA | 93664 |
rs36199276 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122874397 | AGGACACAAACAAAT[-/G]GGAAAAACATTCCAT | 93664 |
rs41281713 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122490372 | CATGGAAAAGAATGG[C/T]TTTGATATTAGCAGT | 93664 |
rs41281716 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122512985 | CTGATGCAAGAAAAC[A/C]GTTACCTTCTATTAA | 93664 |
rs41281719 | snp | C/T | 0.160938 | 0.233598 | intron-variant | CADPS2 | GRCh38.p7 | 7:122629099 | ACATGCTTTCAGATA[C/T]TTGGGATTAAGAGGT | 93664 |
rs41281722 | snp | C/T | 0.00167716 | 0.0289097 | missense | CADPS2 | GRCh38.p7 | 7:122663482 | GCACACGTTTTTCTA[C/T]GTTTTTCTTAAATAC | 93664 |
rs41513151 | snp | C/T | 0.382279 | 0.212137 | intron-variant | CADPS2 | GRCh38.p7 | 7:122322755 | CATTCATGTTGCACA[C/T]TAAGAAAAAAACAAA | 93664 |
rs45489900 | snp | C/T | 0.327662 | 0.237631 | intron-variant | CADPS2 | GRCh38.p7 | 7:122360846 | AAAGAAAGAGATAAT[C/T]ATGAGAATTATTTTT | 93664 |
rs55638895 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122656119 | TTGTCTAGTAATTTT[A/G]AAAAATTACTATAAG | 93664 |
rs55642101 | in-del | -/ATTTTTTTAG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122816258 | CAATTTATTTTTTAG[-/ATTTTTTTAG]CTCCCAAATATGAGA | 93664 |
rs55648500 | in-del | -/AGGTGGGCGGATCAACTGAGGTTG | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122827423 | CACTTTGGGAGGTTG[-/AGGTGGGCGGATCAACTGAGGTTG]GGAGTTTGCGACCAG | 93664 |
rs55659446 | snp | A/T | 0.195526 | 0.243993 | intron-variant | CADPS2 | GRCh38.p7 | 7:122708488 | TATATATATATATAT[A/T]GGATATGTAGATCCA | 93664 |
rs55664480 | snp | A/T | 0.433818 | 0.169443 | intron-variant | CADPS2 | GRCh38.p7 | 7:122492202 | AATAAATAAATAAAT[A/T]AATTAATTAATTAAA | 93664 |
rs55674037 | snp | A/G | 0.445196 | 0.1562 | intron-variant | CADPS2 | GRCh38.p7 | 7:122398609 | GAAAATTAATAAGTC[A/G]CTCTCCATGTTGACA | 93664 |
rs55689539 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122508241 | CCAGCAATTTCATTT[C/T]TACAAGAATACTCCC | 93664 |
rs55728082 | snp | G/T | 0.378372 | 0.214524 | intron-variant | CADPS2 | GRCh38.p7 | 7:122527582 | AAAGATAATACTGAA[G/T]AGAGAGAGAGAGAGA | 93664 |
rs55768795 | snp | A/G | 0.348354 | 0.22984 | intron-variant | CADPS2 | GRCh38.p7 | 7:122837448 | GTTTTTTGTGTCTCT[A/G]TCGCCTTCAGTTGTG | 93664 |
rs55777455 | in-del | -/AT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122579480 | TATATATATATATAT[-/AT]GTCACTTATGTATCC | 93664 |
rs55789434 | in-del | -/ACAC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122762052 | CACACACACACACAC[-/ACAC]GTATATTTATGTGTG | 93664 |
rs55807328 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122738445 | AGAAAACAACATAGT[C/T]TTGGAGATAAAACAA | 93664 |
rs55823131 | snp | C/T | 0.311123 | 0.242413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122809433 | AAGAAAAAAAAAATT[C/T]AGGCAGGCATGGTGG | 93664 |
rs55830112 | in-del | -/TCTC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122398764 | CTCTCTCTCTCTCTC[-/TCTC]CCGCCGCCCTCCCCA | 93664 |
rs55833580 | snp | C/T | 0.226779 | 0.248919 | intron-variant | CADPS2 | GRCh38.p7 | 7:122660681 | TTTGGGAGGCCGAGG[C/T]GGGCGGATCATGAGG | 93664 |
rs55840083 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122492348 | CTGGTCTGCCTCTTA[-/A]TTCTTCTTGTCTTTT | 93664 |
rs55869009 | snp | G/T | 0.213937 | 0.247385 | intron-variant | CADPS2 | GRCh38.p7 | 7:122568583 | TTGATTTTTCACAAA[G/T]ATGTTAAGTAAATTC | 93664 |
rs55869191 | in-del | -/CAT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122696512 | CCATGACCCCATGGT[-/CAT]GGAAGCAGTTATAGC | 93664 |
rs55883532 | in-del | -/AGT | 0.496905 | 0.0392151 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122538140 | TCCCACTTATACAAA[-/AGT]TTCAGTAAAAAAAAA | 93664 |
rs55899881 | in-del | -/ATTT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122526206 | TTTATTTATTTATTT[-/ATTT]GAGGCAGAGTCTCAC | 93664 |
rs55913030 | snp | C/T | 0.399968 | 0.200024 | intron-variant | CADPS2 | GRCh38.p7 | 7:122591435 | TTTATAGATTCAATG[C/T]CATCCCCATCAAGCT | 93664 |
rs55921314 | snp | A/T | 0.0637235 | 0.166737 | intron-variant | CADPS2 | GRCh38.p7 | 7:122662640 | CAGCCTCCCAAAGCA[A/T]TGGGTTACAGGCGTG | 93664 |
rs55926419 | snp | A/C | 0.427575 | 0.175975 | intron-variant | CADPS2 | GRCh38.p7 | 7:122721524 | TAGACCAATAACAGG[A/C]TCTGAAATTGAGGCA | 93664 |
rs55933077 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122609412 | AGAAACAATTCCTCC[A/G]TATCTCATTCATACA | 93664 |
rs55957650 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122541016 | GAAAATGTTAGTGTT[G/T]GAAATAGAAAATGTC | 93664 |
rs55966925 | snp | A/G | 0.0921849 | 0.193893 | intron-variant | CADPS2 | GRCh38.p7 | 7:122692817 | GCTTTCCCATCCACA[A/G]CTCTCACGCACTGTT | 93664 |
rs55975206 | snp | A/G | 0.406296 | 0.19512 | intron-variant | CADPS2 | GRCh38.p7 | 7:122495740 | CCTAGCTGCTTTCCA[A/G]TTTGTACATACTATA | 93664 |
rs55985792 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122783089 | TGGTGGTGGGCGGGC[A/G]CCTGTGGTCCCAGCT | 93664 |
rs55994025 | in-del | -/A | 0.445196 | 0.1562 | intron-variant | CADPS2 | GRCh38.p7 | 7:122398713 | ACTGCAGTCTAGAAC[-/A]GCATTATGTAAAAGG | 93664 |
rs55997702 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | CADPS2 | GRCh38.p7 | 7:122403521 | AACACAAGATGATAT[A/G]TAGTCAATGTATAGA | 93664 |
rs56003036 | snp | A/C | 0.260227 | 0.249791 | intron-variant | CADPS2 | GRCh38.p7 | 7:122854130 | TTTGGGAGGCTGAGG[A/C]GGGTGGATAACTTGA | 93664 |
rs56003675 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122814367 | ATCAAATGGATTACT[A/C]AGAGAAGCATCTGAA | 93664 |
rs56004723 | snp | G/T | 0.389903 | 0.207189 | intron-variant | CADPS2 | GRCh38.p7 | 7:122492111 | TGGGAGGCTGAGGTT[G/T]TAGTGAGACGAGATC | 93664 |
rs56027633 | in-del | -/AGTT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122713231 | GTCTTAAGTCTCGTT[-/AGTT]TTACCAGGAATAGCA | 93664 |
rs56027681 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122736337 | AGGAATCCATTCCCT[C/G]AAATGACTCTGAATT | 93664 |
rs56029436 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122802101 | ATGTATAAAATCTAT[C/T]TATAAAAGCAAATTA | 93664 |
rs56029822 | snp | C/T | 0.0952156 | 0.196321 | intron-variant | CADPS2 | GRCh38.p7 | 7:122686908 | CAGGCTGGTCTCAAA[C/T]TCCTGGCCTCGGGTC | 93664 |
rs56060136 | snp | A/G | 0.397633 | 0.201754 | intron-variant | CADPS2 | GRCh38.p7 | 7:122459410 | CTAGGTTAAATGCAC[A/G]ATATTTTCAAGTATT | 93664 |
rs56060331 | snp | A/G | | | intron-variant, nc-transcript-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122563610 | AATATAACAAATTTA[A/G]TTTTGTTCTTAATCT | 93664 |
rs56078204 | snp | C/T | 0.0256215 | 0.110247 | intron-variant, upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122621961 | TCGCATATATTTTCA[C/T]ATTAAATTTATTTGT | 93664 |
rs56107717 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122366684 | ATATATATATATATA[C/T]GTATATATATATATA | 93664 |
rs56111341 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122333613 | TTAAGACTCAGCTCA[A/G]TCATTCATTATCTCT | 93664 |
rs56120318 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122809420 | AAAAAAAAAAAAAGA[-/A]AAAAAAAAATTTAGG | 93664 |
rs56122498 | snp | C/T | 0.247053 | 0.249983 | intron-variant | CADPS2 | GRCh38.p7 | 7:122673246 | GAATGGGACCCCAGC[C/T]GGTTGCCGCAGCTGG | 93664 |
rs56136329 | in-del | -/AAG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122696517 | ACCCCATGGTCATGG[-/AAG]CAGTTATAGCTAACT | 93664 |
rs56137420 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122443735 | AAAAAAAAAAAAAAA[-/A]TGCTGTCAACTTTTA | 93664 |
rs56144255 | snp | C/G | 0.409041 | 0.192888 | intron-variant | CADPS2 | GRCh38.p7 | 7:122417968 | TGAGGTCAGGAGTTC[C/G]AAACCAGCCTGGCCA | 93664 |
rs56148137 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122758126 | TATAATTTTTAGATA[C/T]TATCTTGATAAAATG | 93664 |
rs56150634 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122830463 | AAGAAGTGAAATACT[C/T]CTGAATAACATGCAA | 93664 |
rs56151803 | snp | A/C | 0.0267878 | 0.112589 | intron-variant | CADPS2 | GRCh38.p7 | 7:122437966 | GCAGAACAGAAAATA[A/C]AATTACATAATACTA | 93664 |
rs56166405 | snp | A/G | 0.0652144 | 0.168387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122644449 | GACACAGCCTTCATA[A/G]TTGTCTTACTGTGCA | 93664 |
rs56184474 | in-del | -/GTGTTGTT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122808242 | TATTAATGGTGCAGT[-/GTGTTGTT]AAACTGCTTCCCTGG | 93664 |
rs56185713 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122575970 | CCAAGAAACTTACAT[C/T]GGCACATTACTATTA | 93664 |
rs56221432 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122508163 | GTTTTGAAATGGAGT[C/T]TTGTAGAACAATTTT | 93664 |
rs56241532 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | CADPS2 | GRCh38.p7 | 7:122453017 | CAAAGTATCATTTAA[A/G]TATGAGATTTTTTTT | 93664 |
rs56249606 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122481561 | CCTGGCCAACGTGGA[A/G]AAACCCCATCTCTAT | 93664 |
rs56250059 | snp | C/T | 0.0825414 | 0.185628 | intron-variant | CADPS2 | GRCh38.p7 | 7:122459492 | CTGGCCTGCAGTGCA[C/T]GAAATTATTAATTTT | 93664 |
rs56259371 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122443700 | TGTCAGTTCCAGTTT[C/T]TGCTTTCTACAAAAA | 93664 |
rs56265223 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122431149 | ATTTAGTAATTGGTT[G/T]GAAAGACTTTTTGCA | 93664 |
rs56287248 | snp | A/T | 0.399968 | 0.200024 | intron-variant | CADPS2 | GRCh38.p7 | 7:122504672 | CCTGGTCTCAAGTGA[A/T]CCTCCCACCTCAGCC | 93664 |
rs56289619 | in-del | -/AT | 0.308908 | 0.242961 | intron-variant | CADPS2 | GRCh38.p7 | 7:122756225 | AATTAATATATATAT[-/AT]TGGTATGTACCAAGT | 93664 |
rs56295954 | snp | A/C | 0.312593 | 0.242037 | intron-variant | CADPS2 | GRCh38.p7 | 7:122818728 | TGACTAGCCCTCCCC[A/C]TCCTGCCCAGCAATT | 93664 |
rs56322746 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122733538 | AAGAGCCAATCCTTC[A/C]AGATGGATCCCAAGT | 93664 |
rs56326140 | snp | A/C | 0.377977 | 0.21476 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122553560 | CAATACAGTCCTTAG[A/C]ACCATCCCAACTGTA | 93664 |
rs56326447 | snp | A/C | 0.223225 | 0.248562 | intron-variant | CADPS2 | GRCh38.p7 | 7:122656307 | TGTTCAATCTCCCAG[A/C]TCCTTCTCTCTAGCA | 93664 |
rs56330633 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122366685 | TATATATATATATAC[A/G]TATATATATATATAC | 93664 |
rs56346012 | snp | A/T | 0.282895 | 0.247826 | intron-variant | CADPS2 | GRCh38.p7 | 7:122355081 | AGAAGTATATGTTAC[A/T]AAGATACAAAAGACT | 93664 |
rs56352082 | in-del | -/A | 0.0138799 | 0.0821421 | intron-variant | CADPS2 | GRCh38.p7 | 7:122713315 | TTAAATCCTGTACTT[-/A]ACACTAGCTCTACAA | 93664 |
rs56353151 | snp | G/T | 0.460813 | 0.134379 | intron-variant | CADPS2 | GRCh38.p7 | 7:122721525 | AGACCAATAACAGGC[G/T]CTGAAATTGAGGCAA | 93664 |
rs56364465 | in-del | -/T | 0.0162398 | 0.0886349 | intron-variant | CADPS2 | GRCh38.p7 | 7:122635930 | ATAGCAGCTCCCACA[-/T]TTTTTTTTGTTTTCC | 93664 |
rs56380009 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | CADPS2 | GRCh38.p7 | 7:122739641 | GCAGTTACATTTAAG[A/G]CATAAAATGGATCAA | 93664 |
rs56389459 | snp | A/G | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122696502 | CTTTAGTCTTCCATG[A/G]CCCCATGGTCATGGA | 93664 |
rs56409307 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122656118 | CTTGTCTAGTAATTT[G/T]GAAAAATTACTATAA | 93664 |
rs56413347 | snp | C/T | 0.0283406 | 0.115616 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122699539 | AAAAAGTAAAAGTCA[C/T]ACTGCTAATTTTTGA | 93664 |
rs56759350 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122732823 | ATACATAATGTATAT[-/T]ATATATAATATACAT | 93664 |
rs56782351 | snp | A/T | 0.397633 | 0.201754 | intron-variant | CADPS2 | GRCh38.p7 | 7:122474093 | CTTCTATTTTCACTG[A/T]GCGTTCTTTAAAGTG | 93664 |
rs56843003 | in-del | -/ACAC | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122774304 | CACACACACACACAC[-/ACAC]TCTGGAAACAAAAGA | 93664 |
rs56929407 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122732817 | TATTATATACATAAT[A/G]TATATTATATATAAT | 93664 |
rs56964412 | snp | A/T | 0.176861 | 0.239062 | intron-variant | CADPS2 | GRCh38.p7 | 7:122712028 | TACATTTTTAAATTT[A/T]AAAAAAAACACTCTT | 93664 |
rs56966499 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122664085 | AAAAAAAAAAAAAAA[-/A]GATGATTAGGAAAAC | 93664 |
rs56967982 | snp | C/T | 0.171704 | 0.237423 | intron-variant | CADPS2 | GRCh38.p7 | 7:122356520 | GCTTATTGTACTCTT[C/T]GGAAGGAAGTTACTA | 93664 |
rs56993717 | in-del | -/T | 0.388398 | 0.208197 | intron-variant | CADPS2 | GRCh38.p7 | 7:122729697 | GCCCATTTTTAACGG[-/T]TTTTTTTTTTTTTTT | 93664 |
rs57012726 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122441440 | AACGGGGTCTGTCTC[C/T]CTAGTTCAATAACTA | 93664 |
rs57042738 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122809433 | AGAAAAAAAAAATTT[-/C]AGGCAGGCATGGTGG | 93664 |
rs57057655 | snp | C/G | 0.136847 | 0.222927 | intron-variant | CADPS2 | GRCh38.p7 | 7:122430609 | CAAAGGAGAAAACTA[C/G]TTGATTTTTAATAGG | 93664 |
rs57107142 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | CADPS2 | GRCh38.p7 | 7:122356790 | CTCTTTCCATCATCT[C/G]CTGTGTCTCTTTGAA | 93664 |
rs57121578 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554883 | TTTTTTTGACAAATA[C/T]GTGTTTTCACATTAT | 93664 |
rs57152656 | in-del | -/AG | 0.435212 | 0.167919 | intron-variant | CADPS2 | GRCh38.p7 | 7:122688768 | CATGGTTGTGGTAAC[-/AG]GGGGAGTTATACACC | 93664 |
rs57164887 | in-del | -/T | 0.195837 | 0.244062 | intron-variant | CADPS2 | GRCh38.p7 | 7:122724738 | TTCACCTTTTTTTTT[-/T]CCCATGTGTTTAAAT | 93664 |
rs57189783 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122642278 | CAGTGAGACTCCATC[C/T]CAAAAAAAAAAAAAA | 93664 |
rs57217914 | in-del | -/A | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122668418 | AAAAAAAAAAAAAAA[-/A]CAAAAACAAACTGAA | 93664 |
rs57260722 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122535146 | TGGTACTTGAGTATC[A/G]TGAACTGACAGTGAT | 93664 |
rs57267990 | in-del | -/A | 0.0267878 | 0.112589 | intron-variant | CADPS2 | GRCh38.p7 | 7:122732804 | ATATACATTATATAT[-/A]TATATACATAATGTA | 93664 |
rs57294714 | snp | A/G | 0.478768 | 0.100824 | intron-variant | CADPS2 | GRCh38.p7 | 7:122397833 | CGGCCACATCCAAGA[A/G]CACTTCTGACACCAT | 93664 |
rs57309842 | snp | C/T | 0.188946 | 0.24243 | intron-variant | CADPS2 | GRCh38.p7 | 7:122356506 | CCCCATCTTCCTTTG[C/T]TTATTGTACTCTTCG | 93664 |
rs57311950 | in-del | -/A/AAAA | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122432661 | AAAAAAAAAAAAAAA[-/A/AAAA]GAAAAAAAGAAAAGA | 93664 |
rs57376495 | snp | A/T | 0.307919 | 0.243198 | intron-variant | CADPS2 | GRCh38.p7 | 7:122841067 | GAAATCACTCAAATA[A/T]ATGGAGGAAGAACAT | 93664 |
rs57389578 | snp | A/G | 0.177824 | 0.239355 | intron-variant | CADPS2 | GRCh38.p7 | 7:122712224 | CGAGGGCAGGACTTC[A/G]CTATGCTCCTTCATC | 93664 |
rs57454175 | snp | C/T | 0.13446 | 0.221699 | intron-variant | CADPS2 | GRCh38.p7 | 7:122432717 | AGTAGATGACAAAAT[C/T]ATGATGAATTTTGGG | 93664 |
rs57466961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122530260 | ACAAATTTCAATATA[A/G]TTTTCAACAATAAGC | 93664 |
rs57496424 | snp | C/G | 0.0551013 | 0.156571 | intron-variant | CADPS2 | GRCh38.p7 | 7:122844124 | CAGAAGCTCCTCACA[C/G]GGCCCCACTAGGGAC | 93664 |
rs57522086 | in-del | -/ATATATATATATATATATATATATATAT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122708545 | TATATATATATATAT[-/ATATATATATATATATATATATATATAT]CTTCCTTGCTCTTAG | 93664 |
rs57556241 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122565321 | AGGAAGATGGACAGG[C/G]AGTATGAGGTTGAGA | 93664 |
rs57673491 | in-del | -/ATGT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122323835 | GTACAACTGTTATGT[-/ATGT]GTATATATATGCATA | 93664 |
rs57716923 | in-del | -/AA/AAA | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122575188 | AAAGTAAAAAAAAAA[-/AA/AAA]GGTGGTGGGAGCATC | 93664 |
rs57717649 | snp | A/C | 0.0711525 | 0.174681 | intron-variant | CADPS2 | GRCh38.p7 | 7:122657935 | CATTACAGAAGCTGC[A/C]ATCAGAGTGAACAGG | 93664 |
rs57776589 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | CADPS2 | GRCh38.p7 | 7:122836924 | AGCTCTGCACCAAGC[A/G]GACCTAATAGACATC | 93664 |
rs57790964 | in-del | -/TT | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122367737 | TTTTTTTTTTTTTTT[-/TT]GCTTAAAACAATAAA | 93664 |
rs57800342 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122392797 | CCATTCTTCCAAAGG[G/T]TTTCTACTTGCACAA | 93664 |
rs57818732 | snp | C/T | 0.136847 | 0.222927 | intron-variant | CADPS2 | GRCh38.p7 | 7:122430537 | TGCATGCCAGAATTA[C/T]AAGTAAAAAAAAGAT | 93664 |
rs57823101 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122806350 | TATGTCATTTTTTTC[C/T]ACTACTGTACCCACA | 93664 |
rs57852366 | in-del | -/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122662395 | TTTTTTTTTTTTTTT[-/T]AAGACGAGTCTTACT | 93664 |
rs57887153 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122732811 | ATTATATATTATATA[C/T]ATAATGTATATTATA | 93664 |
rs57983669 | in-del | -/TCATAT | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122541831 | CATATGTTTATATAT[-/TCATAT]GTTTATATATTCATA | 93664 |
rs58040162 | in-del | -/A/AAA/AAAA | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122659326 | AAAAAAAAAAAAAAA[-/A/AAA/AAAA]CACCGTGGAAAAAAA | 93664 |
rs58136911 | snp | A/C | | | intron-variant, downstream-variant-500B | CADPS2, RNF133 | GRCh38.p7 | 7:122697323 | ACAATAACCTCACAA[A/C]TAAGACATACTATAA | 93664 |
rs58138081 | snp | A/C | 0.0314385 | 0.121371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122830348 | CATTCATTGACACTG[A/C]AACAAATACAGCATA | 93664 |
rs58174606 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122591036 | ATAAAAGTATCTGAA[A/T]TTCCAAATTGTCCCT | 93664 |
rs58187843 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122799620 | AAAAAAAAAAAAAAA[-/A]GAAAAGAAGTATAGC | 93664 |
rs58199807 | snp | A/C | 0.181978 | 0.240568 | intron-variant | CADPS2 | GRCh38.p7 | 7:122712369 | CCCTCTAGAAGCACA[A/C]TCTAAGAACCATCTA | 93664 |
rs58205450 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122435206 | ATGGAAACAACAAAA[A/T]TAAAAAGGCAATGTA | 93664 |
rs58242329 | snp | C/T | 0.388398 | 0.208197 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122542077 | CAACGTGCCAGGCAA[C/T]GTTTTAGTCACTTTA | 93664 |
rs58250195 | in-del | -/GTTTATATATTCATAT | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122541837 | TTTATATATTCATAT[-/GTTTATATATTCATAT]ATATTTATATATATG | 93664 |
rs58309512 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122521450 | TTCTTTTATTTGACC[C/T]CACAAGATTAAGACT | 93664 |
rs58360879 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122323893 | TATATATATATATAT[A/G]TATATATATATATAT | 93664 |
rs58360988 | in-del | -/T | 0.44755 | 0.153212 | intron-variant | CADPS2 | GRCh38.p7 | 7:122387871 | TATTCTAAAGACAGA[-/T]TTTTTTCTTGGTTTC | 93664 |
rs58389347 | snp | A/C | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122642279 | AGTGAGACTCCATCT[A/C]AAAAAAAAAAAAAAA | 93664 |
rs58415210 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | CADPS2 | GRCh38.p7 | 7:122856859 | ATGCTGCACTGAGGT[A/G]AATATTCTTACAAAC | 93664 |
rs58439886 | in-del | -/AGA/GAA | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122678873 | GAAACCATGGCAGAA[-/AGA/GAA]CATAAATTGTGAAGA | 93664 |
rs58478325 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122560841 | GTAGAACCTTGAGGT[A/G]GCATATATTATGAAA | 93664 |
rs58556590 | in-del | -/AT/TA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122684437 | GCATATATATATATA[-/AT/TA]CACACATATATATAC | 93664 |
rs58586210 | in-del | -/T | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122684605 | TAAAATATTCCACAA[-/T]GGATGAGAAATCAAT | 93664 |
rs58587342 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122323883 | ATATTTTATATATAT[-/A]TATATATATATATAT | 93664 |
rs58596737 | snp | C/T | 0.0908922 | 0.192833 | intron-variant | CADPS2 | GRCh38.p7 | 7:122669675 | AGGCGGCTACATTTC[C/T]CCTGTCCTCAGCCTG | 93664 |
rs58597041 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122732825 | ACATAATGTATATTA[-/T]ATATAATATACATTA | 93664 |
rs58697669 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122437809 | AAAGCCTGAAGAAAG[-/A]AAAAAAAAAAAAGCA | 93664 |
rs58812629 | snp | C/T | 0.0659589 | 0.169201 | intron-variant | CADPS2 | GRCh38.p7 | 7:122374090 | TAGGATCCAAGGATG[C/T]TTGAATATAAGCAAG | 93664 |
rs58839161 | snp | C/T | 0.41441 | 0.188333 | intron-variant | CADPS2 | GRCh38.p7 | 7:122411767 | TACTCACATACACAG[C/T]GACATGATTCTGAGG | 93664 |
rs58860616 | in-del | -/AC/TA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122760002 | ATATATATATATATA[-/AC/TA]CACACACACACACGG | 93664 |
rs58869733 | snp | A/G | 0.377582 | 0.214995 | intron-variant | CADPS2 | GRCh38.p7 | 7:122482198 | ACACAAGTGAAGGAG[A/G]ATGGCGATTAAAAAA | 93664 |
rs58891896 | snp | C/T | 0.104504 | 0.2033 | intron-variant | CADPS2 | GRCh38.p7 | 7:122435024 | TTTGTATCAAAAATA[C/T]TGCTGAATTTTTAGA | 93664 |
rs58899394 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122855674 | TAGAAACAGGAATTT[C/T]TAAGTCCTTTAGACA | 93664 |
rs58911261 | in-del | -/TCCCA | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122860150 | CCCAACTTCCTCCCA[-/TCCCA]AGTTCACAAAAAATA | 93664 |
rs58923447 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122802071 | AGCTATAAGATGTCT[A/G]AACAGTGTCACAGCA | 93664 |
rs59000280 | snp | G/T | 0.0618563 | 0.164627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122360555 | CTCTGCAACTCAGGT[G/T]ATATGTTCTTATGAT | 93664 |
rs59044183 | snp | C/T | 0.405429 | 0.195811 | intron-variant | CADPS2 | GRCh38.p7 | 7:122345208 | TTTGCTCACTGCAAC[C/T]TCTGCCTTCCCGGCT | 93664 |
rs59126779 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122812436 | AAGAGAGAGAGAGAG[A/C]GAGCAAGCAAAGAAA | 93664 |
rs59186299 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122882618 | CCACCAAGGAACCCT[-/T]TTTTTTTTTTTTTTT | 93664 |
rs59190953 | in-del | -/AATAAATAAATAAATA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122878673 | ATAAATAAATAAATA[-/AATAAATAAATAAATA]CAAAGTTGTCATAAG | 93664 |
rs59217839 | in-del | -/TTTATATATT | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122541838 | TTATATATTCATATG[-/TTTATATATT]CATATATATTTATAT | 93664 |
rs59273835 | in-del | -/AA | 0.179425 | 0.239831 | intron-variant | CADPS2 | GRCh38.p7 | 7:122695967 | ACAAGTACCCCACAC[-/AA]GAGTACACAGAGCTG | 93664 |
rs59329850 | in-del | -/A/AA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122608227 | TAAAAAAAAAAAAAA[-/A/AA]GAAGGCACAGTTTTT | 93664 |
rs59410664 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122679277 | TCCTGGGGGGGGGGG[-/G]CTCTAAAATGGCCAC | 93664 |
rs59469931 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122809431 | AAAAGAAAAAAAAAA[A/T]TTAGGCAGGCATGGT | 93664 |
rs59557479 | snp | A/T | 0.194902 | 0.243853 | intron-variant | CADPS2 | GRCh38.p7 | 7:122356507 | CCCATCTTCCTTTGC[A/T]TATTGTACTCTTCGG | 93664 |
rs59563343 | snp | C/T | 0.199564 | 0.24486 | intron-variant | CADPS2 | GRCh38.p7 | 7:122351954 | TTCAAAGAGAAGTTT[C/T]TTTTAAATATTAAAA | 93664 |
rs59594807 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122432661 | AAAAAAAAAAAAAAA[-/A]GAAAAAAAGAAAAGA | 93664 |
rs59616910 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122731683 | GAGGGGAAAAAAAAA[-/A]CCCTTCAATTAACAA | 93664 |
rs59653845 | in-del | -/GT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122527652 | TGTGTGTGTGTGTGT[-/GT]TTCCTGCAAGTGGTG | 93664 |
rs59716073 | snp | C/T | 0.0912534 | 0.193131 | intron-variant | CADPS2 | GRCh38.p7 | 7:122587458 | TCTCATTCCTTTTTA[C/T]GGCTGTATGGTATTC | 93664 |
rs59739895 | in-del | -/G/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122775981 | TTCAAAAATTTTTTT[-/G/T]CTAGAGAAGTTAGAT | 93664 |
rs59830160 | snp | A/T | 0.0314385 | 0.121371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122830346 | TCCATTCATTGACAC[A/T]GCAACAAATACAGCA | 93664 |
rs59838743 | in-del | -/T | 0.314175 | 0.247355 | intron-variant | CADPS2 | GRCh38.p7 | 7:122828248 | TAACCATTTCTACTA[-/T]TTTTTTATCATTTAC | 93664 |
rs59855207 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122575011 | TGATAAGATGCAACG[C/G]GAAGCACAAAACATT | 93664 |
rs59875049 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122820560 | TTTTGTTTTTTGTTT[G/T]TTTTTTTTTTTTTTT | 93664 |
rs59895150 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | CADPS2 | GRCh38.p7 | 7:122663862 | AAATCCTTTAGAGTG[A/G]TGTCCTTATGAATGT | 93664 |
rs59899381 | in-del | -/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122668253 | AATTCCATTTTTTTT[-/T]ACTGGGGTGTCTAGA | 93664 |
rs59910018 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122710816 | TATTATATATAATTA[A/G]AGGCATATATGTCTG | 93664 |
rs59952403 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | CADPS2 | GRCh38.p7 | 7:122827433 | AGGTTGGGAGTTTGC[A/G]ACCAGCCTGACCAAC | 93664 |
rs60038458 | snp | C/T | 0.307671 | 0.243257 | intron-variant | CADPS2 | GRCh38.p7 | 7:122845690 | GCAGGTTCACATGCA[C/T]AGGGGAGAGTCTTCA | 93664 |
rs60052865 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122500257 | TTTGTTTCTGACTCA[A/G]TGTCTTCATAATACG | 93664 |
rs60094398 | in-del | -/ATATATATATATATATAT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122708555 | TATATATATATATAT[-/ATATATATATATATATAT]CTTCCTTGCTCTTAG | 93664 |
rs60107640 | in-del | -/AA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122640950 | AAAAAAAAAAAAAAA[-/AA]TTGTTGACCCACTAG | 93664 |
rs60110967 | snp | C/G | 0.323671 | 0.238899 | intron-variant | CADPS2 | GRCh38.p7 | 7:122868115 | CTGCAGACTCTCCCT[C/G]GAAGTAGTTTCTGCA | 93664 |
rs60253193 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | CADPS2 | GRCh38.p7 | 7:122604459 | TGGACCAGCCCCAGG[C/T]ATATCTCCTGGACTG | 93664 |
rs60343818 | in-del | -/AT | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122556911 | TTCTTTCCCTAGAGT[-/AT]GCAATGGTTTCCTGA | 93664 |
rs60352846 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122809196 | AAATATGGCAAGGGT[C/T]TAAGACAAAAGTGTG | 93664 |
rs60364724 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122858626 | CATCGCTTGCTTTTA[-/A]CCTTCATTCTCTAAA | 93664 |
rs60487995 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122809804 | GTGTCCAGTCCACCC[-/C]TCATAGGGTAAGAGC | 93664 |
rs60519662 | snp | C/G | 0.0337553 | 0.125452 | intron-variant | CADPS2 | GRCh38.p7 | 7:122750314 | CAGAATAAATTTTTA[C/G]TATAAATATGTCCTA | 93664 |
rs60559343 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122812437 | AGAGAGAGAGAGAGA[A/G]AGCAAGCAAAGAAAG | 93664 |
rs60560320 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122576484 | GCACCCTTTTGATGC[C/T]GCTGGTTGATGTGTT | 93664 |
rs60569506 | in-del | -/CACA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122746638 | ACACAGACACACACA[-/CACA]GACACACACACACAC | 93664 |
rs60674414 | snp | C/G | 0.44638 | 0.154709 | intron-variant | CADPS2 | GRCh38.p7 | 7:122390256 | CTAGACAACACCATT[C/G]TGATACTACAGTGAA | 93664 |
rs60730410 | snp | A/T | 0.369346 | 0.219673 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122553035 | GTCATGTAGCTGGAA[A/T]GCCAGTTCTCCCACT | 93664 |
rs60797530 | in-del | -/A | 0.474992 | 0.108989 | intron-variant | CADPS2 | GRCh38.p7 | 7:122472312 | TCATGTAAGAGAAAT[-/A]AAAGAATAATGAGAA | 93664 |
rs60821982 | snp | A/G | 0.137187 | 0.223099 | intron-variant | CADPS2 | GRCh38.p7 | 7:122430367 | TCAGGAAACAGTAGG[A/G]ACTGTTATCAAATGT | 93664 |
rs60844157 | in-del | -/A | 0.262985 | 0.249663 | intron-variant | CADPS2 | GRCh38.p7 | 7:122796034 | TACAAAATCAATGAG[-/A]AAAAAAATCACTAAC | 93664 |
rs60932238 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122407250 | GCCTTTGAAGATTTT[A/C]AGATTCATAAGGTAC | 93664 |
rs60966196 | in-del | -/GATAA | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122490717 | AATTCTTTCACATAA[-/GATAA]TATTTTGCATTTTAA | 93664 |
rs60977505 | snp | A/T | 0.0252325 | 0.109451 | intron-variant | CADPS2 | GRCh38.p7 | 7:122467549 | AGATTATTTTATATA[A/T]AAAACTACAGTCATG | 93664 |
rs60986310 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122732830 | ATGTATATTATATAT[-/A]ATATACATTATATAT | 93664 |
rs60987464 | in-del | -/AATAAATA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122878681 | ATAAATAAATAAATA[-/AATAAATA]CAAAGTTGTCATAAG | 93664 |
rs61030047 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122574290 | GTTCTACCAAAAAAT[C/T]TAAAAATTTGCCCAG | 93664 |
rs61030114 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | CADPS2 | GRCh38.p7 | 7:122666929 | GTGAACTACTCTGCC[A/G]TGCAGTAAGACACAC | 93664 |
rs61064830 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122689375 | ACCACCTTCCTGATC[C/T]GATTAACCTTATCAG | 93664 |
rs61097528 | in-del | -/G | 0.625 | 0.125 | intron-variant | CADPS2 | GRCh38.p7 | 7:122427143 | TGTGTGTGTGTGTGT[-/G]TTTAACTTTTTCTTT | 93664 |
rs61170517 | in-del | -/CTCT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122439670 | ACTTTATCATTCTCT[-/CTCT]ATCAAATTCAATTAT | 93664 |
rs61203849 | in-del | -/T | 0.0670745 | 0.170406 | intron-variant | CADPS2 | GRCh38.p7 | 7:122429273 | ATGCACACACACAGC[-/T]TTTTTTTAAAATATA | 93664 |
rs61292857 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122747929 | CTGCTGCCCCCAAAT[C/T]ATGTCATCTTATCCT | 93664 |
rs61331991 | in-del | -/AA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122812421 | TTTGGAAAAAAAAAA[-/AA]GAGAGAGAGAGAGAG | 93664 |
rs61409877 | in-del | -/TT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122708487 | ATATATATATATATA[-/TT]GGATATGTAGATCCA | 93664 |
rs61417913 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122323899 | TATATATATATATAT[A/T]TATATATATATATAT | 93664 |
rs61418661 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122364299 | GTGTGCCTGTAGCTT[C/T]TCAGGAAGCTGAGGT | 93664 |
rs61517518 | in-del | -/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122552793 | TTTTTTTTTTTTTTT[-/T]ATTATTGTGCCATTC | 93664 |
rs61533752 | in-del | -/C | 0.0123036 | 0.0774623 | intron-variant | CADPS2 | GRCh38.p7 | 7:122874323 | TAGGAATACAACTTA[-/C]AAGGGATGTGAAGGA | 93664 |
rs61588302 | snp | C/T | 0.104504 | 0.2033 | intron-variant | CADPS2 | GRCh38.p7 | 7:122425789 | TCAAATACTGAATCA[C/T]ATAAAGTCTATAGCA | 93664 |
rs61594727 | snp | C/T | 0.391954 | 0.205789 | intron-variant | CADPS2 | GRCh38.p7 | 7:122604944 | CACAGAGTGTACTTA[C/T]ACAAACCTAGGCAGT | 93664 |
rs61656656 | in-del | -/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122631694 | TTTTCTTTTTTTTTT[-/T]AATTTCAGATTTGGA | 93664 |
rs61692498 | snp | C/T | 0.393803 | 0.204501 | intron-variant | CADPS2 | GRCh38.p7 | 7:122596813 | GTCTAGGTTCCTTTA[C/T]AGCAACACAAAACCC | 93664 |
rs61707435 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122354773 | TTTCTTTCTCACTCT[G/T]TTTTCAAATGTCTGT | 93664 |
rs61730957 | snp | C/T | 0.0253123 | 0.109615 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122388702 | TTGCAGTGCATCAAG[C/T]TTCCAAAAAAGGTCT | 93664 |
rs61743033 | snp | A/G | 0.000430863 | 0.0146713 | missense | CADPS2 | GRCh38.p7 | 7:122490227 | TCATCACTGGCAAAG[A/G]TTACAGTATCTCCTT | 93664 |
rs61997179 | snp | C/T | 0.00240068 | 0.0345626 | synonymous-codon, utr-variant-5-prime | CADPS2 | GRCh38.p7 | 7:122621571 | AGAGTTCTGTGAACG[C/T]TTTAATTTTTGTAAT | 93664 |
rs62473063 | snp | A/G | 0.133435 | 0.221162 | intron-variant | CADPS2 | GRCh38.p7 | 7:122325212 | AATTATTGTGAACCT[A/G]CTTCCTTCAGGTAAC | 93664 |
rs62473064 | snp | A/G | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122328161 | CACACACACACACAC[A/G]CACGCACACACCTTA | 93664 |
rs62473065 | snp | A/G | 0.17332 | 0.23795 | intron-variant | CADPS2 | GRCh38.p7 | 7:122333880 | ATTTAAATATTTATA[A/G]ATATAAATTTATATA | 93664 |
rs62473066 | snp | A/G | 0.219349 | 0.248114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122336520 | TACATATAGAGGTCA[A/G]AATTTCTAGACCATC | 93664 |
rs62473067 | snp | A/G | 0.209084 | 0.246629 | intron-variant | CADPS2 | GRCh38.p7 | 7:122337832 | ACAATATAGAAACAG[A/G]CTTGACTATGACTAT | 93664 |
rs62473068 | snp | A/T | 0.209084 | 0.246629 | intron-variant | CADPS2 | GRCh38.p7 | 7:122337835 | ATATAGAAACAGGCT[A/T]GACTATGACTATCTT | 93664 |
rs62473069 | snp | A/G | 0.207864 | 0.246424 | intron-variant | CADPS2 | GRCh38.p7 | 7:122338213 | ACCACCCTGGGCAAC[A/G]TGGTGAAACCCTGTC | 93664 |
rs62473070 | snp | A/C | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122338973 | TCTTGCAATGTTGCT[A/C]AGGCTGTTCTTGAAC | 93664 |
rs62473071 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122340875 | AAAAAAAAAAAAAAG[A/G]ACATTGGTGTAAGAG | 93664 |
rs62473072 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | CADPS2 | GRCh38.p7 | 7:122352434 | TTTTGGCTTAAGTGA[C/T]GACTCAGGGTGCTAG | 93664 |
rs62474589 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122361250 | TTTTTTTTTTTTAAA[A/T]TGAGATGGAGGCTTG | 93664 |
rs62474590 | snp | C/T | 0.282369 | 0.247896 | intron-variant | CADPS2 | GRCh38.p7 | 7:122363573 | AAGTTGCAGCTCTGC[C/T]GCTGTCTGGCTACGA | 93664 |
rs62474591 | snp | A/G | 0.336702 | 0.234484 | intron-variant | CADPS2 | GRCh38.p7 | 7:122366302 | AGAACGTTAATATAT[A/G]ATAATAAAATAATAC | 93664 |
rs62474592 | snp | C/T | 0.281841 | 0.247964 | intron-variant | CADPS2 | GRCh38.p7 | 7:122368098 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 93664 |
rs62474593 | snp | C/T | 0.282105 | 0.24793 | intron-variant | CADPS2 | GRCh38.p7 | 7:122370228 | TGCATTTTATGTTTG[C/T]TAGTGTGTCTCCTCC | 93664 |
rs62474594 | snp | C/T | 0.271162 | 0.249103 | intron-variant | CADPS2 | GRCh38.p7 | 7:122372089 | TAACACTAATAAATG[C/T]TACTATTATATTACT | 93664 |
rs62474595 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122373191 | GCTATTTTTTTTTTA[A/T]TATCCTGAAGTTTAA | 93664 |
rs62474596 | snp | C/T | 0.284733 | 0.247575 | intron-variant | CADPS2 | GRCh38.p7 | 7:122376816 | ATGATTATAAACTTA[C/T]ATGGTTGTATACTTA | 93664 |
rs62474597 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122382598 | ATAGGTTTTTTTTCC[C/T]ATTTAGTATAACAGA | 93664 |
rs62474598 | snp | A/C/T | 0.0532157 | 0.154195 | intron-variant | CADPS2 | GRCh38.p7 | 7:122397008 | TGAGGCCTGTGTATA[A/C/T]GCCTCATACTTTGTA | 93664 |
rs62474599 | snp | C/G/T | 0.00597646 | 0.0543919 | intron-variant | CADPS2 | GRCh38.p7 | 7:122405030 | GAGCTTGCAGTGAGC[C/G/T]GAGATCGCGTCATTG | 93664 |
rs62474600 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122434337 | ATATTGAAAAAGGTA[A/G]GGGAAAAAAAAAAGA | 93664 |
rs62474601 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122455167 | CCTAACTAGTCCTCA[A/G]ACACAGGAAGCAAGC | 93664 |
rs62474602 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122481467 | ATGATAGGGCTGGGC[A/G]CTGTGGCTCATGCCT | 93664 |
rs62474604 | snp | C/T | 0.00637319 | 0.05614 | intron-variant | CADPS2 | GRCh38.p7 | 7:122496522 | TTCATTTTTAATATA[C/T]GCATTTATGTTTATT | 93664 |
rs62474605 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122506725 | GTGCTGCTAGAGTTA[A/T]TTAAAAAAAAAAAAA | 93664 |
rs62474620 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122512094 | GTTACTTTTTAGCCA[A/G]GAAAAAAAAAATAGG | 93664 |
rs62474621 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | CADPS2 | GRCh38.p7 | 7:122514676 | AGGTGCACATAAAGG[C/T]GTATGCTGTAGGGAT | 93664 |
rs62474622 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | CADPS2 | GRCh38.p7 | 7:122520217 | ATAAAATGGTTCTTG[A/G]CAATAGATTTATTGA | 93664 |
rs62474623 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122522437 | ATTAAAAAAAAATTT[A/T]ACTGATATGTATTTT | 93664 |
rs62474624 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122527609 | GAGAGAGAGAGAGAG[A/T]GAGAGAGAGTGTGTG | 93664 |
rs62474625 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122527611 | GAGAGAGAGAGAGAG[A/T]GAGAGAGTGTGTGTG | 93664 |
rs62474626 | snp | A/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122527613 | GAGAGAGAGAGAGAG[A/T]GAGAGTGTGTGTGTG | 93664 |
rs62474627 | snp | C/T | | | intron-variant, upstream-variant-2KB | CADPS2, LOC105375481 | GRCh38.p7 | 7:122529297 | TTAATGGAATCATTT[C/T]ACAGACTCATACATT | 93664 |
rs62474628 | snp | C/T | | | intron-variant, nc-transcript-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122530334 | TTTTTTTTTTTTTCC[C/T]ACTAGCTTTCAAGTT | 93664 |
rs62474629 | snp | C/T | 0.185472 | 0.241529 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122544134 | CATGTACAAGAATGT[C/T]CACAGTAGCAATACA | 93664 |
rs62474630 | snp | A/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122545545 | CTTGGGAAGCAACTG[A/T]ATTTTTTTTTTAGTA | 93664 |
rs62474631 | snp | G/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122547888 | TCTAGAGTAGAGCTG[G/T]CAAAGGTCTTTAGAA | 93664 |
rs62474632 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122567979 | AATAACCCAGTTAAA[A/G]GGCAGAGGTGTGTCA | 93664 |
rs62474633 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122567981 | TAACCCAGTTAAAAG[A/G]CAGAGGTGTGTCAGA | 93664 |
rs62474634 | snp | C/T | 0.25045 | 0.25 | intron-variant | CADPS2 | GRCh38.p7 | 7:122569162 | AAAATCTCCTTAAGC[C/T]GATAAGCAACTTCAG | 93664 |
rs62474635 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122569536 | GAAAAAACTACTTTA[A/G]AGTTCATATGGAACC | 93664 |
rs62474636 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122570437 | TACACTGTTGGTGGG[A/T]CTGTAAACTAGTTCA | 93664 |
rs62474637 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122570546 | GGGTATATACCCAAA[C/G]GACTATAAATCATGC | 93664 |
rs62474638 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122570549 | TATATACCCAAAGGA[C/T]TATAAATCATGCTGC | 93664 |
rs62474639 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122575082 | GTCATGAAAAAAATA[G/T]TCTTATTTTTTTCTT | 93664 |
rs62474640 | snp | A/C | 0.167785 | 0.236095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122595159 | GATGTGTTATATGAA[A/C]CAAAAAAAAAAAAAT | 93664 |
rs62474641 | snp | A/C | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122595161 | TGTGTTATATGAACC[A/C]AAAAAAAAAAAATCC | 93664 |
rs62474642 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122597860 | TATTAAGCATATCTT[A/T]CAATGAGAGCATACA | 93664 |
rs62474643 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122619479 | AAAAAAAAAAAAATT[A/T]AGCCAGGCATTGTGT | 93664 |
rs62474644 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122621071 | TCATCATGACTGGAT[A/T]ATTTTTTTTTTTTAG | 93664 |
rs62474645 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122630450 | GGAGGTAAAACTAGA[C/T]ACACACAGTGGTTCT | 93664 |
rs62476012 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CADPS2 | GRCh38.p7 | 7:122319804 | GAGAAATATGTATCT[C/T]GCTTTACACAGAAAA | 93664 |
rs62476013 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122323892 | ATATATATATATATA[C/T]ATATATATATATATA | 93664 |
rs62476014 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122323897 | TATATATATATATAT[A/G]TATATATATATATAT | 93664 |
rs62476015 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122323903 | TATATATATATATAT[A/T]TATATATATATATAT | 93664 |
rs62482229 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122640510 | ATAGAGAGAGAGAGA[A/G]AGAAAAAAAAAGAAG | 93664 |
rs62482254 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122649355 | TTGGGTTCCCACACT[C/T]CCAAACCAGCTCTAT | 93664 |
rs62482255 | snp | A/G | 0.322007 | 0.239405 | intron-variant | CADPS2 | GRCh38.p7 | 7:122651775 | GGCAGAAAAGAGCAG[A/G]GTCTAGATAGCTATA | 93664 |
rs62482256 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122653068 | ACCAAACGATGGCCA[C/T]CGATGTCATGTGGCA | 93664 |
rs62482257 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122658932 | GTAAAAAAAAAAGTT[A/T]CTCGTACTTATGGCT | 93664 |
rs62482258 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | CADPS2 | GRCh38.p7 | 7:122673873 | GCAGGAGGTGGTGCC[C/T]GTTGGGGAGGCTTGG | 93664 |
rs62482259 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122686204 | GCAAATTATCTAAAA[A/T]CTATTAGTTTACTCA | 93664 |
rs62482466 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122814249 | AAATCTTAACAGAAA[C/T]AACCAAATTAAGGAG | 93664 |
rs62482468 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122818504 | CCTTCTTTCCCTCCC[A/G]CCTGTCCCCTCAGTA | 93664 |
rs62482470 | snp | A/G | 0.357664 | 0.225629 | intron-variant | CADPS2 | GRCh38.p7 | 7:122819238 | GAATGCCCGCAGCCC[A/G]GGATTCCTCCTAAGC | 93664 |
rs62482471 | snp | C/T | 0.311859 | 0.242226 | intron-variant | CADPS2 | GRCh38.p7 | 7:122819413 | ACTGCCCGATCGCCT[C/T]GGAAGCCCCCTAGAC | 93664 |
rs62482475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122820806 | CCTCGTGATCCGCCC[A/G]CCTCGGCCTCCCAAA | 93664 |
rs62482476 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122820811 | TGATCCGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 93664 |
rs62482477 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122820812 | GATCCGCCCGCCTCG[A/G]CCTCCCAAAGTGCTG | 93664 |
rs62482478 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122820836 | AGTGCTGGGATTACA[G/T]GCGTGAGCCACCGCG | 93664 |
rs62482479 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122820838 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC | 93664 |
rs62482480 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122820849 | CAGGCGTGAGCCACC[A/G]CGCCCGGCCGACCTT | 93664 |
rs62482481 | snp | A/G/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122820851 | GGCGTGAGCCACCGC[A/G/T]CCCGGCCGACCTTAC | 93664 |
rs62482482 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122820854 | GTGAGCCACCGCGCC[C/T]GGCCGACCTTACTGT | 93664 |
rs62482484 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122822548 | AATATAAGAAGGCAG[A/G]AATGTCAGGCCTCTG | 93664 |
rs62482485 | snp | C/T | 0.331874 | 0.236213 | intron-variant | CADPS2 | GRCh38.p7 | 7:122828035 | GCCAATAACTGTGGA[C/T]GTCTGATTTTCCTTT | 93664 |
rs62482486 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | CADPS2 | GRCh38.p7 | 7:122829871 | AATAATTTATTTAAG[C/T]CAAGCTAATTCAAAA | 93664 |
rs62482487 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122832320 | AAAAAAAAAAAAACC[A/C]ACCCATGTGTGCACA | 93664 |
rs62482523 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122859851 | TTTGTAATTTTTTCC[C/T]AAGTATCTTCAATCT | 93664 |
rs62482524 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | CADPS2 | GRCh38.p7 | 7:122861975 | TTCCCTGTTAAAATG[A/G]GGAAAATTTTAGACC | 93664 |
rs62483576 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122726480 | CCCCCACTGTGACTG[A/T]GCTAACACAGGTACA | 93664 |
rs62483577 | snp | A/C | 0.493107 | 0.0583 | intron-variant | CADPS2 | GRCh38.p7 | 7:122731594 | CAAAAACGAAGAGCA[A/C]ACACTTGTAGAATTT | 93664 |
rs62483578 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122747806 | TACCTTCAAAACGCC[A/G]TCCCATTCATGTTGT | 93664 |
rs62483579 | snp | A/G/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122753883 | ACACTGCAGGTCACC[A/G/T]AAAACTTTTTTTTTT | 93664 |
rs62483604 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122759388 | TTGAAATGCAAAGGT[C/T]AGGAAAGAAATCAAA | 93664 |
rs62483605 | snp | C/T | 0.410568 | 0.191619 | intron-variant | CADPS2 | GRCh38.p7 | 7:122761156 | GAAAACACTGAAGAC[C/T]TCTTCTCTGGGAAAA | 93664 |
rs62483608 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122769601 | GGAAATGTTATTCAT[C/T]CATTTGCTAAAAGCC | 93664 |
rs62483611 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122777953 | ACTTGACTTTGGAAC[C/T]GGGTAACAGGCAGAG | 93664 |
rs62483612 | snp | G/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122783733 | ATAATTGACATTGTG[G/T]ACTTTCCGAGTAAAA | 93664 |
rs62483614 | snp | A/G | 0.307176 | 0.243374 | intron-variant | CADPS2 | GRCh38.p7 | 7:122794490 | CTGGCTATTTTGTCT[A/G]TCAGACTTCAACTCC | 93664 |
rs62483615 | snp | A/G | 0.296619 | 0.245615 | intron-variant | CADPS2 | GRCh38.p7 | 7:122795334 | ATCATGAACACTTCC[A/G]TGCACATAAACTAGA | 93664 |
rs62483617 | snp | C/T | 0.300169 | 0.244914 | intron-variant | CADPS2 | GRCh38.p7 | 7:122801537 | AATCACCACATGTAA[C/T]AGTGAAGAAATATTA | 93664 |
rs62640526 | snp | C/T | 0.451234 | 0.14834 | intron-variant | CADPS2 | GRCh38.p7 | 7:122706263 | TATATTCAAGGAATA[C/T]ATATATGTTTATATA | 93664 |
rs62640527 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | CADPS2 | GRCh38.p7 | 7:122706271 | AGGAATATATATATG[C/T]TTATATATTCAAGGA | 93664 |
rs62651332 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122706180 | TATATTCAAGGAATA[C/T]ATATATATGCTTATA | 93664 |
rs62651333 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122706209 | TATATTCAAGGAATA[C/T]ATATATGCTTATATA | 93664 |
rs66524549 | snp | G/T | 0.178144 | 0.239451 | intron-variant | CADPS2 | GRCh38.p7 | 7:122675955 | CAACAAACCTGCACG[G/T]TCTGTACATGCATCC | 93664 |
rs66552780 | snp | A/G | 0.179425 | 0.239831 | intron-variant | CADPS2 | GRCh38.p7 | 7:122692901 | AGGGTCAGCAGCTTA[A/G]CTCTCTCTCTCTGGG | 93664 |
rs66554243 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122669357 | ATATATATATATATT[-/A]TTTTTTTTTTGAGAA | 93664 |
rs66587423 | in-del | -/A | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122636483 | GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 93664 |
rs66621319 | in-del | -/AAAA | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122481183 | GAGCAAGACTCCGTC[-/AAAA]AAAAAAAAAAAAAAA | 93664 |
rs66649699 | in-del | -/CA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122747841 | TCATTGTGCCTTTGC[-/CA]ACAGTTTGCTTCCTC | 93664 |
rs66656487 | snp | A/G | 0.473451 | 0.112115 | intron-variant | CADPS2 | GRCh38.p7 | 7:122519637 | TAGGAAACAAAGCAC[A/G]AAGACAACTAAATAT | 93664 |
rs66699011 | snp | A/G | 0.179105 | 0.239737 | intron-variant | CADPS2 | GRCh38.p7 | 7:122691485 | ACCCATAGGTCTTGT[A/G]CCTACTGAAGAGCCT | 93664 |
rs66798940 | snp | G/T | 0.174932 | 0.238463 | intron-variant | CADPS2 | GRCh38.p7 | 7:122728609 | TATTTGTTCTTTACA[G/T]TTTTGGGGGACTGCA | 93664 |
rs66884888 | snp | C/T | 0.176861 | 0.239062 | intron-variant | CADPS2 | GRCh38.p7 | 7:122713845 | GTTATAATGTACAGG[C/T]CAACTTTAAAAAACA | 93664 |
rs66970091 | snp | A/G | 0.179425 | 0.239831 | intron-variant | CADPS2 | GRCh38.p7 | 7:122707885 | ACTTCATAGTTTCAT[A/G]TAACAAAACTAGTTT | 93664 |
rs67003887 | in-del | -/A | 0.410061 | 0.192043 | intron-variant | CADPS2 | GRCh38.p7 | 7:122640934 | GCAAGACTCTATCTC[-/A]AAAAAAAAAAAAAAA | 93664 |
rs67047809 | in-del | -/TAAAGTTTAGA | 0.0341408 | 0.126114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122352364 | TTCATTTTTAGCTTT[-/TAAAGTTTAGA]TGGACTGGGATGGGT | 93664 |
rs67149486 | in-del | -/C/TT | 0.414741 | 0.188044 | intron-variant | CADPS2 | GRCh38.p7 | 7:122801009 | GTTCACTTGAATTTT[-/C/TT]TTTTTTTTTTTTTTT | 93664 |
rs67203312 | in-del | -/ACAATCTCGGC | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122686746 | CTGGTGTGCAGTGGC[-/ACAATCTCGGC]TCACTGCAACCTCCG | 93664 |
rs67210777 | snp | A/T | 0.178785 | 0.239642 | intron-variant | CADPS2 | GRCh38.p7 | 7:122707667 | GAAATTAAATGAATC[A/T]TAACGAGATCTGAGG | 93664 |
rs67232921 | in-del | -/TTT/TTTT | 0.625 | 0.125 | intron-variant | CADPS2 | GRCh38.p7 | 7:122878278 | TCTTTCCCTTCCCAC[-/TTT/TTTT]TTTTTTTTTTTTTTT | 93664 |
rs67253616 | snp | C/T | 0.180064 | 0.240019 | intron-variant | CADPS2 | GRCh38.p7 | 7:122730027 | GAAAATGAGTGAATA[C/T]TGGAGGTAAGAAACT | 93664 |
rs67263105 | snp | C/G | 0.180064 | 0.240019 | intron-variant | CADPS2 | GRCh38.p7 | 7:122707275 | CTAGGCAGAATAAAA[C/G]AGTTACATGCAAGTT | 93664 |
rs67310961 | snp | C/G | 0.148661 | 0.22854 | intron-variant | CADPS2 | GRCh38.p7 | 7:122625693 | AGCCTGCCTACTTGT[C/G]CTATGGATTCTGGAC | 93664 |
rs67327643 | snp | A/G | 0.179425 | 0.239831 | intron-variant | CADPS2 | GRCh38.p7 | 7:122688757 | ATTTTATGGCTACAT[A/G]GTTGTGGTAACGGGG | 93664 |
rs67394622 | in-del | -/A | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122585477 | AAAAAAAAAAAAAAA[-/A]GGCAGGAAAAGAGGA | 93664 |
rs67402535 | multinucleotide-polymorphism | AG/CA | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122795744 | CTATGACATACCCAC[AG/CA]CAAACATCATACTGA | 93664 |
rs67549880 | snp | C/T | 0.184838 | 0.241358 | intron-variant | CADPS2 | GRCh38.p7 | 7:122720761 | AGATTGAAAACTGAA[C/T]GTTCATAAGATTACT | 93664 |
rs67582850 | in-del | -/TG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122427133 | GCCGTGTGTGTGTGT[-/TG]GTGTGTGTGTTTTAA | 93664 |
rs67590838 | snp | A/C | 0.282895 | 0.247826 | intron-variant | CADPS2 | GRCh38.p7 | 7:122863622 | TAAAATTACAAAAAA[A/C]GTTCAAATGAATGAA | 93664 |
rs67645613 | in-del | -/T | 0.5 | 0 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122538141 | ACTTATACAAAAGTT[-/T]CAGTAAAAAAAAAAG | 93664 |
rs67660520 | in-del | -/TATG | 0.469247 | 0.120128 | intron-variant | CADPS2 | GRCh38.p7 | 7:122323830 | ATAAAGTACAACTGT[-/TATG]TATGTGTATATATAT | 93664 |
rs67759336 | snp | C/T | 0.180383 | 0.240111 | intron-variant | CADPS2 | GRCh38.p7 | 7:122685781 | CCAGGGCAATCAATA[C/T]TTGTTGAATGAATCA | 93664 |
rs67765659 | snp | A/G | 0.180383 | 0.240111 | intron-variant | CADPS2 | GRCh38.p7 | 7:122686559 | TCTGCAGTGAGCTTA[A/G]GAATTTGCATTTCTA | 93664 |
rs67776758 | in-del | -/CA | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122640482 | ACACACACACACACA[-/CA]GAGATAGAGAGAGAG | 93664 |
rs67787586 | in-del | -/ATAAG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122490714 | TAAAATTCTTTCACA[-/ATAAG]TAATATTTTGCATTT | 93664 |
rs67803746 | snp | A/G | 0.181978 | 0.240568 | intron-variant | CADPS2 | GRCh38.p7 | 7:122714961 | AAACGTCATACAGCT[A/G]TAAGTGGATGAACCA | 93664 |
rs67817582 | snp | C/T | 0.181978 | 0.240568 | intron-variant | CADPS2 | GRCh38.p7 | 7:122707657 | TTTTTTGCAAGAAAT[C/T]AAATGAATCATAACG | 93664 |
rs67820520 | in-del | -/TCTT | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122546550 | TAGACCTCTGCTGAT[-/TCTT]CTTAAGCTTTTTCCT | 93664 |
rs67843561 | in-del | -/AA | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122664962 | AGACCCCATATCTAC[-/AA]AAAAAAAAAAAAAAA | 93664 |
rs67930883 | in-del | -/ATCTT | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122424786 | ATTCGTCCCTGTGAG[-/ATCTT]AGCTTTTCTTACTTC | 93664 |
rs67938929 | in-del | -/A/AA | 0.625 | 0.125 | intron-variant | CADPS2 | GRCh38.p7 | 7:122447057 | TGGGGGAATGTGGTC[-/A/AA]AAAAAAAAAAAAAAA | 93664 |
rs67969832 | snp | C/T | 0.179744 | 0.239925 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122700455 | CCGATTTTATTTTCA[C/T]ACATCCCTGCACATT | 93664 |
rs68008900 | in-del | -/A | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122762015 | TATATATATATATAT[-/A]TTTTTTTTTTTTTTT | 93664 |
rs68012966 | snp | G/T | 0.331179 | 0.236453 | intron-variant | CADPS2 | GRCh38.p7 | 7:122816350 | TTCCAGTGCCATCTG[G/T]GTTGTTGCAAATGAC | 93664 |
rs68031621 | in-del | -/ATAT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122708462 | TATATATGTGTGTGG[-/ATAT]ATATATATATATATA | 93664 |
rs68122497 | snp | A/T | 0.383246 | 0.211531 | intron-variant | CADPS2 | GRCh38.p7 | 7:122336621 | TTCAACAGTCTCTTA[A/T]AAAATTGGTAGAGAG | 93664 |
rs68130351 | in-del | -/C | 0.48955 | 0.071525 | intron-variant | CADPS2 | GRCh38.p7 | 7:122369128 | GAAGAATTTTTGTTT[-/C]CCCCCCCCCCCCCCT | 93664 |
rs71159788 | in-del | -/ATATATATATATATATATAT | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122323903 | GATAATGTATTTGCC[-/ATATATATATATATATATAT]ATATATATATATATA | 93664 |
rs71159790 | in-del | -/GTGT/GTGTGT/GTGTGTGT | 0.26078 | 0.249767 | intron-variant | CADPS2 | GRCh38.p7 | 7:122328132 | AAGGTGTGTGCGTGC[-/GTGT/GTGTGT/GTGTGTGT]GTGTGTGTGTGTGTG | 93664 |
rs71159791 | in-del | -/AAA/AAAA/AAAAA | 0.441568 | 0.160629 | intron-variant | CADPS2 | GRCh38.p7 | 7:122345918 | AGATAGCCATTTAAC[-/AAA/AAAA/AAAAA]AAAAAAAAAAAAAAG | 93664 |
rs71159797 | in-del | -/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122425451 | ACCATGCCTGGATAA[-/T]TTTTTTTTTTTTTTT | 93664 |
rs71159798 | in-del | -/ACAC/ACACAC | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122426459 | GAAGCTTTTTAAAAG[-/ACAC/ACACAC]ACACACATTTATATT | 93664 |
rs71159801 | in-del | -/GAAG | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122511280 | AGAGAGTTTGGAAAT[-/GAAG]GAAGGAATTGTAAAA | 93664 |
rs71159802 | in-del | -/ACCACCACCACCACC | 0 | 0 | intron-variant, upstream-variant-2KB | CADPS2, LOC105375481 | GRCh38.p7 | 7:122528146 | TTTTCTGTTCTGCTT[-/ACCACCACCACCACC]ACCACCACCACCACC | 93664 |
rs71161304 | in-del | -/AA | 0 | 0 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122541363 | CTCTGCTAAAAATAC[-/AA]AAAAAAAAAAAAAAA | 93664 |
rs71161306 | in-del | -/TTTTTT | 0 | 0 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122559787 | CTCTTTTTCTTTTCC[-/TTTTTT]TTTTTTTTTTTTTTT | 93664 |
rs71161307 | in-del | -/GTGTGC | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122564852 | TGTGTGTGTGTGTGT[-/GTGTGC]GTGTGCATGTGTGTG | 93664 |
rs71161308 | in-del | -/C | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122574376 | TCACTGCAGCCTCCA[-/C]CCTGCTAGGCTCAAG | 93664 |
rs71161311 | in-del | -/T | 0.355505 | 0.226646 | intron-variant | CADPS2 | GRCh38.p7 | 7:122610152 | AAGCCCCCAGTGCTC[-/T]TTTTTTTTTTTTATT | 93664 |
rs71161313 | in-del | -/AAAAAAAAAAAAAA | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122637195 | AGACCCTGTCTCAGG[-/AAAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 93664 |
rs71161314 | in-del | -/ATATATAT | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122645678 | AAAATCCCAAGATAT[-/ATATATAT]ATATATATATATATA | 93664 |
rs71161320 | in-del | -/T | 0.377385 | 0.215112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122669356 | TCTCAAAAAAAAAAA[-/T]ATATATATATATATA | 93664 |
rs71161321 | in-del | -/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122670886 | GAAGAAGTTTGGGAC[-/T]TTTTTTTTTTTTTTT | 93664 |
rs71161322 | in-del | -/CA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122679266 | AGAGCCCCCCCCCCC[-/CA]CAGGAATGCATTCTT | 93664 |
rs71161324 | in-del | -/AGAA | 0 | 0 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122700581 | ATAACAATGAGAGAC[-/AGAA]AGATTTAGGTATTGT | 93664 |
rs71161326 | in-del | -/ATAT/ATATTCCTTGAATATATAAGCATATATATAT | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122706286 | TAAGCATATATATAT[lengthTooLong]TCCTTGAATATATAA | 93664 |
rs71161327 | in-del | -/ATAT | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122708480 | CTACATATCCAATAT[-/ATAT]ATATATATATATATA | 93664 |
rs71161328 | in-del | -/ATATATATATATATATATATATATATAT | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122708521 | TATATATATATATAT[-/ATATATATATATATATATATATATATAT]CTCGAATACAATATG | 93664 |
rs71161329 | in-del | -/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122710065 | GTTGGCAGAAGGTCA[-/T]TTTTTTTTTTTTTTT | 93664 |
rs71161330 | in-del | -/T | 0.249886 | 0.25 | intron-variant | CADPS2 | GRCh38.p7 | 7:122715711 | TTGGCTTTTTTTTTT[-/T]CTTTGCAATGCGTTG | 93664 |
rs71161331 | in-del | -/AATTCTGTGAAGA | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122722667 | AAAGTAGTTTTTTCC[-/AATTCTGTGAAGA]AAGTCATTGGTAGCT | 93664 |
rs71161332 | in-del | -/AT | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122725348 | CATATATACCTATAC[-/AT]ATATATATATAAAAG | 93664 |
rs71161440 | in-del | -/T | 0.339203 | 0.233544 | intron-variant | CADPS2 | GRCh38.p7 | 7:122757911 | CTCTGTTGATGTTAG[-/T]TTTTTTTTTCCCTGT | 93664 |
rs71312898 | in-del | -/T | 0.496314 | 0.0427728 | intron-variant | CADPS2 | GRCh38.p7 | 7:122405667 | TAAGCCGGTTTTTTG[-/T]TTTGTTTTGTTTGAG | 93664 |
rs71324637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122822452 | TGGAGAGAGAATGGG[C/T]GATGTTTCTCAGGGC | 93664 |
rs71529457 | in-del | AAA/GAAT | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122809431 | CCACCATGCCTGCCT[AAA/GAAT]TTTTTTTTTTCTTTT | 93664 |
rs71529458 | multinucleotide-polymorphism | AGG/GGC | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122722972 | CAGCTGTCTACATAT[AGG/GGC]TAGCCAGTTTTCCCA | 93664 |
rs71529460 | multinucleotide-polymorphism | ACACA/TCTCT | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122527625 | CACACACACACACAC[ACACA/TCTCT]CACACACTCTCTCTC | 93664 |
rs71529461 | in-del | ATTT/TTA | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122501340 | AAATCATAGTTTTAA[ATTT/TTA]CCAAATGTAATATCT | 93664 |
rs71530092 | in-del | -/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122408193 | TATTTTTTTTTTTTT[-/T]ACCAATTACCCTATT | 93664 |
rs71530093 | in-del | -/A | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122428471 | TATATATATATATAT[-/A]TTTTTTTTTTTTTGA | 93664 |
rs71530096 | in-del | -/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122447056 | TTTTTTTTTTTTTTT[-/T]TTGACCACATTCCCC | 93664 |
rs71530098 | in-del | -/TTTTAA | 0.482309 | 0.0923707 | intron-variant | CADPS2 | GRCh38.p7 | 7:122480355 | AAAAAATAAGCTTCT[-/TTTTAA]GATTTATACTTCATT | 93664 |
rs71530100 | in-del | -/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122489590 | TTAAGGTACAAGGGG[-/G]AAAAAAGTTGGCTTT | 93664 |
rs71530101 | in-del | -/A | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122506747 | AAAAAAAAAAACAAA[-/A]CAAACTACACCAGAG | 93664 |
rs71530102 | in-del | -/CAT | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122514254 | TTTTCAATATTTTAT[-/CAT]AATCCTTTATTCTGA | 93664 |
rs71531904 | in-del | -/GTCTCT | 0.5 | 0 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539772 | TTTCTCTCTGTCTCT[-/GTCTCT]CTCTTTCTGTTTCTC | 93664 |
rs71531907 | in-del | -/A/AA | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122608213 | AGCGAGACTCCGTCT[-/A/AA]AAAAAAAAAAAAAAG | 93664 |
rs71531908 | in-del | -/AAGG | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122644116 | AGGAAGGAAGGAAGG[-/AAGG]AACAAACGAAGGAAA | 93664 |
rs71531909 | multinucleotide-polymorphism | GA/TT | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122649899 | TCAATGATTTTTTTT[GA/TT]TTTTTTTTTTTTTTT | 93664 |
rs71531912 | in-del | -/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122681146 | GGTGGGGGGAGGGGG[-/G]AGGGATAGCATTGGG | 93664 |
rs71531915 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122749962 | TCACCTGTGAGGTTA[-/A]AAAAAAAAAAAAAAG | 93664 |
rs71531916 | in-del | -/ACC | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122780893 | GACTACAAACAATGC[-/ACC]AAAAATCACTCTTAC | 93664 |
rs71531917 | in-del | -/A | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122790416 | AAAAAAAAAAAAAAA[-/A]GAAAAGAATTAAGTT | 93664 |
rs71546731 | snp | A/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122477031 | AGGAGAGGAGTGGAG[A/T]GGAGAGGAGAGGAGA | 93664 |
rs71571068 | snp | A/C | 0.5 | 0 | utr-variant-3-prime | CADPS2 | GRCh38.p7 | 7:122319969 | CAAACAAACAAACAA[A/C]CAAAAAAAGGAAACA | 93664 |
rs71571069 | snp | C/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122351104 | GGCGTGGTGATTCAT[C/G]CCTGTAATCCCAGCA | 93664 |
rs71571070 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122367783 | TAGTTCTGTAGTTCA[A/G]AAGCCTAACAAAGGC | 93664 |
rs71571071 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122367786 | TTCTGTAGTTCAGAA[A/G]CCTAACAAAGGCTTC | 93664 |
rs71571072 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122367860 | GGAGGCTCTAGGGGA[A/G]AATTTGTTTTCTTCA | 93664 |
rs71571073 | snp | G/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122367912 | ATTCATGGTTCATGG[G/T]CTCTATCCTCCATCT | 93664 |
rs71571074 | snp | C/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122367938 | CATCTTCAAAGCTGG[C/G]AACATAGCATCTCTC | 93664 |
rs71571075 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122367945 | AAAGCTGGCAACATA[A/G]CATCTCTCTAACCCT | 93664 |
rs71571076 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122385610 | CAATCCTTTACGCAT[A/C]AAGGTTTTCTAACCT | 93664 |
rs71571077 | snp | C/T | 0.1652 | 0.235179 | intron-variant | CADPS2 | GRCh38.p7 | 7:122408498 | GGGTTGATCTCAGCT[C/T]ACTGCGACCTCTGCC | 93664 |
rs71573096 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | CADPS2 | GRCh38.p7 | 7:122409790 | GCTGTATAATTCCCT[C/T]CCTAGGGTATTACTT | 93664 |
rs71573097 | snp | C/G | 0.0984431 | 0.198823 | intron-variant | CADPS2 | GRCh38.p7 | 7:122433472 | GCAATGGCACCACCT[C/G]GGCTCACTGTAACTT | 93664 |
rs71573098 | snp | A/G | 0.0988009 | 0.199095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122437812 | GCCTGAAGAAAGAAA[A/G]AAAAAAAAAGCACAG | 93664 |
rs71573099 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122443990 | CAAGTCTTCCCCCCA[A/G]ATCACAGGCAACTAC | 93664 |
rs71573100 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122470055 | TGGGCAGATGGAAGA[A/G]GATGGTAATGGGAAA | 93664 |
rs71573101 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | CADPS2 | GRCh38.p7 | 7:122500148 | GTTTAAAATTCCATT[G/T]CTATATATTTCTCAA | 93664 |
rs71573102 | snp | A/T | 0.156319 | 0.231784 | intron-variant | CADPS2 | GRCh38.p7 | 7:122523030 | ATGCTACGATAAACA[A/T]GGAGGTACAGGTATC | 93664 |
rs71574703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122534188 | AAAAGCGTGATTCTG[A/G]TTTTTATCTAAACTC | 93664 |
rs71574704 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122536048 | CAAGGCATCCTTATA[A/C]AAATTGCCTTTTGTA | 93664 |
rs71574705 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122588988 | GAACTGGGAGCCAGG[A/G]AACTTGCCTGACTGA | 93664 |
rs71574706 | snp | G/T | 0.190833 | 0.242898 | intron-variant | CADPS2 | GRCh38.p7 | 7:122595411 | CTTTGGGGCCAGTCA[G/T]TTGGGGTTATAAAAA | 93664 |
rs71574707 | snp | A/G | 0.164873 | 0.23506 | intron-variant | CADPS2 | GRCh38.p7 | 7:122604008 | TTGATTGTAATAATC[A/G]TTATACAATATATAC | 93664 |
rs71574708 | snp | C/T | 0.0637235 | 0.166737 | intron-variant | CADPS2 | GRCh38.p7 | 7:122624607 | GTTTAAATGTTTTTG[C/T]TACAAATTAGAGCAG | 93664 |
rs71574709 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | CADPS2 | GRCh38.p7 | 7:122630961 | TTGATTAATATGATT[C/T]AAAATCAAACAGAAA | 93664 |
rs71574710 | snp | G/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122632733 | TTTTTGTTTTCATTG[G/T]AATTGCTTTTGTGGA | 93664 |
rs71574711 | snp | G/T | 0.0456336 | 0.143994 | intron-variant | CADPS2 | GRCh38.p7 | 7:122646519 | TGAAGAATGGAGAAG[G/T]AGGAATTCCAAATGA | 93664 |
rs71574712 | snp | A/C | 0.0460142 | 0.144533 | intron-variant | CADPS2 | GRCh38.p7 | 7:122654880 | TCTAGATGCCATTAA[A/C]ACACTTGTGATTCAA | 93664 |
rs71574713 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | CADPS2 | GRCh38.p7 | 7:122665934 | TGCTTTAAATATTCA[C/T]GTATCAAAGACAATG | 93664 |
rs71574714 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | CADPS2 | GRCh38.p7 | 7:122678112 | GTCCTTGTGGTAATG[A/G]ACTTTGGAAAGTTAT | 93664 |
rs71574715 | snp | G/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122681139 | TGTTGTAGGGTGGGG[G/T]GAGGGGGAGGGATAG | 93664 |
rs71574716 | snp | C/T | 0.0795731 | 0.182906 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698916 | AACCTTGAGTAGATG[C/T]ATCTCTCTCTTCTCC | 93664 |
rs71574717 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | CADPS2 | GRCh38.p7 | 7:122711524 | TGCAACCAACTTTTT[C/T]TCCAATCCAGAATGC | 93664 |
rs71574718 | snp | G/T | 0.353371 | 0.227628 | intron-variant | CADPS2 | GRCh38.p7 | 7:122790028 | AAACAAATATTAAGT[G/T]TTTTTTTTTTTTTTT | 93664 |
rs71574719 | snp | A/C | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122800696 | GGAGGAAAAGAGCAA[A/C]CAAAAAATTCAGCTG | 93664 |
rs71574721 | snp | A/G | 0.312593 | 0.242037 | intron-variant | CADPS2 | GRCh38.p7 | 7:122821503 | CATGCCCTGAGTCAG[A/G]TAACTAAAATACCTT | 93664 |
rs71574722 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122855936 | AATACCCCAGTCTTC[C/T]TACAGCTACAGTTTG | 93664 |
rs71574724 | snp | A/G | 0.00835141 | 0.0640778 | upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122887244 | TCCTGCAGACTCAAG[A/G]CAAGAGAGATTTTAT | 93664 |
rs71585570 | snp | C/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122818535 | ATTAGAAAGACTCAG[C/T]GACGCTTGGGGTTGG | 93664 |
rs71726905 | in-del | -/TG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122469824 | AAGCAGGTGTGTGTC[-/TG]TGTGTGTGTGTGTGT | 93664 |
rs71753783 | in-del | -/AGG | 0.0685596 | 0.171987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122504380 | TTTCATGTTGGGTAC[-/AGG]ACACAGGTGTTACTA | 93664 |
rs71755031 | in-del | -/A/AAA/AAAA | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122575179 | CATTATAATAAAAGT[-/A/AAA/AAAA]AAAAAAAAAAGGTGG | 93664 |
rs71790470 | in-del | -/CA | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122550775 | ACAGACACACACACA[-/CA]CACAAACCAGGAAAA | 93664 |
rs71908581 | in-del | -/A | 0.0513262 | 0.151752 | intron-variant, upstream-variant-2KB | CADPS2, LOC105375481 | GRCh38.p7 | 7:122529232 | GTACCTTCCCACCCC[-/A]AAAAAGCAACACTAA | 93664 |
rs71917807 | in-del | -/ACAC | 0.49889 | 0.0235361 | intron-variant | CADPS2 | GRCh38.p7 | 7:122746629 | AGCTAAAACACACAG[-/ACAC]ACACACACAGACACA | 93664 |
rs71946219 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122331159 | TTCTATTGTCTGTTA[-/T]TTTTTTTTTAACTTA | 93664 |
rs72001976 | in-del | -/ATTATT | 0.351635 | 0.228408 | intron-variant | CADPS2 | GRCh38.p7 | 7:122805155 | AAAGCATTTTCAATC[-/ATTATT]ATTATTATTATTGTT | 93664 |
rs72017363 | in-del | -/ACAT | 0.0569829 | 0.158885 | intron-variant | CADPS2 | GRCh38.p7 | 7:122441037 | TTCATTTAAGGTAAC[-/ACAT]ACACTGGAATAATTG | 93664 |
rs72068486 | in-del | -/TG | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122550064 | TGAATATTTAGTGTG[-/TG]AATGCAGTTTATGTA | 93664 |
rs72073098 | in-del | -/GGA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122504381 | TTCATGTTGGGTACA[-/GGA]CACAGGTGTTACTAT | 93664 |
rs72094544 | in-del | -/ATA | 0.116488 | 0.211364 | intron-variant | CADPS2 | GRCh38.p7 | 7:122594376 | TGGGTAATGACTTTC[-/ATA]ATAAGAAAAATCCTG | 93664 |
rs72108160 | in-del | -/TGG | 0.164128 | 0.234789 | intron-variant | CADPS2 | GRCh38.p7 | 7:122594356 | TATTGGGAAATGGGT[-/TGG]GGTGGGTAATGACTT | 93664 |
rs72162571 | in-del | -/AT | 0.49975 | 0.0111793 | intron-variant | CADPS2 | GRCh38.p7 | 7:122579451 | ATAAAATTGCATCGA[-/AT]ATATATATATATATA | 93664 |
rs72188819 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122338928 | ATCATGCTAGGCTAA[-/T]TTTTTTTTTTTTTTT | 93664 |
rs72212858 | in-del | -/AC | 0.330482 | 0.236691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122774270 | GACATAGATAGATAT[-/AC]ACACACACACACACA | 93664 |
rs72222150 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122447032 | ATAAGTAGCTCCCTC[-/T]TTTTTTTTTTTTTTT | 93664 |
rs72240155 | in-del | -/TA | 0.0170251 | 0.090679 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122556910 | CTTCTTTCCCTAGAG[-/TA]TGCAATGGTTTCCTG | 93664 |
rs72243070 | in-del | -/TA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122645417 | ACATATACACACATG[-/TA]TATATGTGTGTATAT | 93664 |
rs72390156 | in-del | -/A | 0.470424 | 0.117954 | intron-variant | CADPS2 | GRCh38.p7 | 7:122462371 | ATAAACTGTTAAGAG[-/A]AAAAAAAAGAATTAA | 93664 |
rs72404042 | in-del | -/TCT | 0.0482946 | 0.147699 | intron-variant | CADPS2 | GRCh38.p7 | 7:122409407 | AAAAATTCCTAAAGG[-/TCT]TCTTAAAGTTAACTT | 93664 |
rs72427049 | in-del | -/GA | 0.0322114 | 0.122752 | intron-variant | CADPS2 | GRCh38.p7 | 7:122598315 | CTATGTTTTTTAAAT[-/GA]GAGTATTATAATAGC | 93664 |
rs72451273 | in-del | -/TTT | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122518446 | GTCTTAAAAAATTTG[-/TTT]TTTATGTTATTATCA | 93664 |
rs72489712 | in-del | -/TCTT | 0.286042 | 0.247388 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539826 | GTCTTTCTGTCTCTC[-/TCTT]TCTTTCTTTAGTAAA | 93664 |
rs72500216 | in-del | -/TTTTC | 0.029116 | 0.117091 | intron-variant | CADPS2 | GRCh38.p7 | 7:122493842 | GATAAACATTTGAAG[-/TTTTC]TTTTCTGTGAGTTTC | 93664 |
rs72600543 | in-del | -/AG/CA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122747843 | ATTGTGCCTTTRCAC[-/AG/CA]ASTTTGCTTCCTCTG | 93664 |
rs72604206 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122874144 | TTTTCTTTTGCTGTG[-/A]CAAAGCTCTTTAGTT | 93664 |
rs72607711 | snp | A/T | 0.192088 | 0.2432 | intron-variant | CADPS2 | GRCh38.p7 | 7:122486523 | TAAAACTTGAACAGA[A/T]AAGAAGTTGGTTCCT | 93664 |
rs72607712 | snp | G/T | 0.179425 | 0.239831 | intron-variant | CADPS2 | GRCh38.p7 | 7:122497010 | TATATACCTGGGATT[G/T]TTACTTCTTTCTCGG | 93664 |
rs72607713 | snp | A/G | 0.179425 | 0.239831 | intron-variant | CADPS2 | GRCh38.p7 | 7:122693692 | TGGGCGTAGTGGCTC[A/G]TGCCTATAAACCTAG | 93664 |
rs72607714 | snp | A/G | 0.185155 | 0.241444 | intron-variant | CADPS2 | GRCh38.p7 | 7:122725398 | ATATGTGGATGGATG[A/G]ATGGATGGATAGATT | 93664 |
rs72617285 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122818697 | CACACCTGGTCCGAC[G/T]TACAGTTTCGTTCCC | 93664 |
rs73214169 | snp | C/T | 0.228253 | 0.249052 | intron-variant | CADPS2 | GRCh38.p7 | 7:122321481 | CCATGTTTACTTTTT[C/T]CTTTTCTTTTTTTTG | 93664 |
rs73214170 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122321839 | GCAGCTAAACATGAC[C/T]GGTATTTTATTACTA | 93664 |
rs73216104 | snp | C/G | 0.283158 | 0.247791 | intron-variant | CADPS2 | GRCh38.p7 | 7:122364273 | TAAAAAAATTGGCTG[C/G]GCATGGTGGCGTGTG | 93664 |
rs73216113 | snp | A/T | 0.353371 | 0.227628 | intron-variant | CADPS2 | GRCh38.p7 | 7:122386209 | TTTATATAATTTTAA[A/T]TTGAAAAGATGAAAA | 93664 |
rs73216116 | snp | A/G | 0.429837 | 0.173662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122392720 | AGGGCCTGCAATGAT[A/G]CAGTACTGTTTTTTA | 93664 |
rs73216117 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122396264 | TCACTCTGACAACCA[A/G]TTAGTCATCAAGACT | 93664 |
rs73216118 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122397083 | AACCCATATGTACAA[A/G]ATCGGACTGCTAAAA | 93664 |
rs73216119 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122401702 | TAAACTGATTGCCCA[C/T]TAAATTACCTCTTTA | 93664 |
rs73216120 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | CADPS2 | GRCh38.p7 | 7:122408715 | TACTGGTGTAAGCCA[C/T]GGCACCTGGCTTCAA | 93664 |
rs73216125 | snp | C/G | 0.415727 | 0.187175 | intron-variant | CADPS2 | GRCh38.p7 | 7:122433434 | TTGAGATGGAGTTTT[C/G]CTCTTGTTGCCTAGG | 93664 |
rs73216127 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122434408 | ACCCAAGCAAACTTG[C/T]TTATAACATTGCATA | 93664 |
rs73216192 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122442134 | TATTTCTAGTTCTAC[A/G]TATTCCTACTGCACA | 93664 |
rs73216196 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | CADPS2 | GRCh38.p7 | 7:122448175 | TGTAGAATAAATCAA[C/T]GTTGAGAAGTCATTC | 93664 |
rs73216200 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | CADPS2 | GRCh38.p7 | 7:122455457 | TGGCCACTGTACATA[G/T]GGCTGCCATCTAACA | 93664 |
rs73218203 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122476906 | GTATAGTCTTAGTTT[C/T]CATGAATTTATGGAA | 93664 |
rs73218204 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | CADPS2 | GRCh38.p7 | 7:122477961 | TCTTTCACTTTAAAG[C/T]TATCTCATGAACTAA | 93664 |
rs73218205 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122480524 | TTCATCAATTGGGTG[G/T]TTTTTTATGTAGTGA | 93664 |
rs73218208 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122487384 | ATATTCATCTTATTG[C/T]AGTGGTCTGGAACTG | 93664 |
rs73218218 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122548882 | AAAATAAAGTTAGCA[A/G]AAAAATAAACACACA | 93664 |
rs73218224 | snp | A/G | 0.380138 | 0.213458 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122557756 | GAACTATGGCACACC[A/G]GCTGGCTATTTGCCA | 93664 |
rs73218225 | snp | C/T | 0.381891 | 0.212379 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122558434 | TTCTCTTAACCTTTC[C/T]GTATGCATTTCTGCT | 93664 |
rs73218228 | snp | G/T | 0.377385 | 0.215112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122581508 | TCAAAAAATTAGCAT[G/T]TTGGACTATAAAAAA | 93664 |
rs73218230 | snp | A/G | 0.387074 | 0.209071 | intron-variant | CADPS2 | GRCh38.p7 | 7:122586009 | ATTATGTATAACAGT[A/G]AACACTTAAGCAAGA | 93664 |
rs73218231 | snp | A/G | 0.38555 | 0.210062 | intron-variant | CADPS2 | GRCh38.p7 | 7:122590041 | GTTTGCACTATGCAA[A/G]ATGACCAGTGGTTCA | 93664 |
rs73218232 | snp | A/C | 0.39325 | 0.204889 | intron-variant | CADPS2 | GRCh38.p7 | 7:122590056 | AATGACCAGTGGTTC[A/C]ACGTGAATTCCATCA | 93664 |
rs73218233 | snp | A/C | 0.39325 | 0.204889 | intron-variant | CADPS2 | GRCh38.p7 | 7:122590473 | TCTTTTCAAGACTTA[A/C]GACATTCCCCTTGTA | 93664 |
rs73218234 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122593133 | CTAGGCCATGAGGAT[A/T]ACATTCATCCCACAA | 93664 |
rs73218235 | snp | A/G | 0.387642 | 0.208697 | intron-variant | CADPS2 | GRCh38.p7 | 7:122594105 | ATAAAATTTTTTATT[A/G]TGATGGAAAGATAAC | 93664 |
rs73218236 | snp | A/T | 0.417034 | 0.18601 | intron-variant | CADPS2 | GRCh38.p7 | 7:122603078 | TCTTCAATGACATCA[A/T]CTGAGACACAAAACC | 93664 |
rs73218237 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | CADPS2 | GRCh38.p7 | 7:122605480 | ATATGATCCCACCAC[C/T]GATGAAAAATACCTG | 93664 |
rs73218238 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | CADPS2 | GRCh38.p7 | 7:122613625 | AGACAGAAAGTAAAT[C/T]AGTGGTTGGTTAAGG | 93664 |
rs73218240 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122622722 | CCAGTGCACAGAACC[A/G]GCTGGAGGATGAAAG | 93664 |
rs73218247 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122633294 | TGGGCAGTATGATCC[A/G]TTTAATGATACTGAT | 93664 |
rs73218248 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | CADPS2 | GRCh38.p7 | 7:122634870 | TATTTTCCTTAATTT[C/T]AAGGAAGTTTTTGAT | 93664 |
rs73220261 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | CADPS2 | GRCh38.p7 | 7:122636383 | AGGATATGAATTTCA[C/T]GGTTGGAATTTCTTT | 93664 |
rs73220268 | snp | A/G | 0.112631 | 0.208878 | intron-variant | CADPS2 | GRCh38.p7 | 7:122659493 | TCCCAGGACTGTGGG[A/G]TAACATGGGTAACAG | 93664 |
rs73220269 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | CADPS2 | GRCh38.p7 | 7:122659503 | GTGGGATAACATGGG[C/T]AACAGAAACATGGGT | 93664 |
rs73220277 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122671635 | AATGAGCCTCGTCTT[A/G]TGAGAAGCAGCTGAT | 93664 |
rs73220278 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122672409 | GTGTCGAAGCTGTCA[C/T]GGGAATTCCTTACAT | 93664 |
rs73220280 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | CADPS2 | GRCh38.p7 | 7:122677056 | CCCCCATAGCTTAAC[C/T]ATTTGTTCAATAAAT | 93664 |
rs73220282 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122689503 | CAGGAACAGTTATTG[C/T]TAAGGGATAGAACCA | 93664 |
rs73220284 | snp | C/T | 0.209084 | 0.246629 | intron-variant | CADPS2 | GRCh38.p7 | 7:122692008 | GTGGATTGCCAAGTC[C/T]GCATATGGCCTTTGG | 93664 |
rs73220285 | snp | C/T | 0.179425 | 0.239831 | intron-variant | CADPS2 | GRCh38.p7 | 7:122692553 | TTCCACTGGGGCCCA[C/T]CCAGGCAGCACCGCT | 93664 |
rs73220287 | snp | C/T | 0.0209421 | 0.100162 | intron-variant, utr-variant-5-prime | CADPS2, RNF148 | GRCh38.p7 | 7:122702835 | AAGATAGCTTGTTGG[C/T]GGCAGATTACTAAAG | 93664 |
rs73220288 | snp | G/T | 0.221439 | 0.248363 | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122704353 | TCCTTACAGGTAGAC[G/T]TTTTTTTTTTCATGT | 93664 |
rs73220291 | snp | C/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122710004 | ATGGCACATATGTAA[C/G]TAACCTGCACATTGT | 93664 |
rs73220293 | snp | C/T | 0.217851 | 0.247924 | intron-variant | CADPS2 | GRCh38.p7 | 7:122712421 | ATTATTTCACTCATT[C/T]GAATATTTATCAAGA | 93664 |
rs73220294 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | CADPS2 | GRCh38.p7 | 7:122713270 | TGAATTTTGCAAGTT[C/T]AATTAATTTTTAAGC | 93664 |
rs73220296 | snp | A/G | 0.217851 | 0.247924 | intron-variant | CADPS2 | GRCh38.p7 | 7:122718406 | AGGAGAGAAGTAGAA[A/G]GAGGGAGGAAGAAAG | 93664 |
rs73220297 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122718586 | CACAGGTTTTTCTCC[A/G]TTGTTAACAGTCTAG | 93664 |
rs73220302 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122724456 | GTACACATGATAATA[A/T]AAATTAAGTGCTGAA | 93664 |
rs73222407 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122729370 | TTGATTTAATTTCCT[A/T]TGGATAAATACCAAG | 93664 |
rs73222408 | snp | A/C | 0.0681886 | 0.171594 | intron-variant | CADPS2 | GRCh38.p7 | 7:122732303 | TAAACCGAATATCTG[A/C]AGGTACAACCACTAT | 93664 |
rs73222409 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122732326 | ACCACTATAAGAACA[A/G]ACAGAAAACTTTTTT | 93664 |
rs73222410 | snp | C/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122746638 | ACACAGACACACACA[C/G]ACAGACACACACACA | 93664 |
rs73222415 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122804935 | AAGCTCTGGGGATTG[C/G]TAAATAGAATTCTTA | 93664 |
rs73224234 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122846624 | ACTCTTTAAATATAG[A/G]AGCCAATAATTTTAA | 93664 |
rs73224235 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122851924 | TATAGACTATTTAAA[G/T]CATCTTTCATGCATC | 93664 |
rs73224241 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122870498 | GAAAGGAGAGATGTT[A/G]ATCAAAGGGTACAAC | 93664 |
rs73431526 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | CADPS2 | GRCh38.p7 | 7:122416841 | ATTAAGTGCAGTTAC[C/T]TGAAATTCTGCTACA | 93664 |
rs73431531 | snp | A/G | 0.172028 | 0.23753 | intron-variant | CADPS2 | GRCh38.p7 | 7:122420039 | CATTTCCAGAGTCTT[A/G]GAGAGGTTGAAGGTG | 93664 |
rs73431532 | snp | A/C | 0.0678174 | 0.1712 | intron-variant | CADPS2 | GRCh38.p7 | 7:122420324 | ACACTATCTTAAGTA[A/C]AAACTCTGAGAGTAC | 93664 |
rs73431535 | snp | A/G | 0.104859 | 0.203554 | intron-variant | CADPS2 | GRCh38.p7 | 7:122428263 | TACGTAAAAATCACC[A/G]TTGCCTTAGCATGAA | 93664 |
rs73431538 | snp | A/G | 0.136166 | 0.22258 | intron-variant | CADPS2 | GRCh38.p7 | 7:122430847 | TCCTTTTATTCTGCA[A/G]ATTTGTGCTGCCAGT | 93664 |
rs73431539 | snp | C/G | 0.135825 | 0.222405 | intron-variant | CADPS2 | GRCh38.p7 | 7:122431541 | GTGCAAATTTAACTA[C/G]ACAAGCTCGTCAAGG | 93664 |
rs73431544 | snp | C/T | 0.046775 | 0.145601 | intron-variant | CADPS2 | GRCh38.p7 | 7:122435751 | ATTATTCATTGAAAG[C/T]AACCTAAATGTTCAT | 93664 |
rs73431546 | snp | A/T | 0.0652144 | 0.168387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122438769 | TCTTCCAGGGACCCA[A/T]GACACCATTAAAGCA | 93664 |
rs73431553 | snp | C/G | 0.0726307 | 0.176182 | intron-variant | CADPS2 | GRCh38.p7 | 7:122450306 | GTTCCAAATCACATG[C/G]ATGCAACATAGCAGA | 93664 |
rs73431561 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122453428 | TATGCATTGACAATG[A/T]TCACAAAAGCTCAAC | 93664 |
rs73431563 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | CADPS2 | GRCh38.p7 | 7:122453849 | AGTCAGGGGAAGCTC[A/G]CTTGTGTCAACCTTC | 93664 |
rs73431568 | snp | C/G | 0.0463947 | 0.145069 | intron-variant | CADPS2 | GRCh38.p7 | 7:122458674 | AAAGCAATCATCTGA[C/G]TCTATAAAGATCTAA | 93664 |
rs73431574 | snp | C/T | 0.11963 | 0.213316 | intron-variant | CADPS2 | GRCh38.p7 | 7:122460959 | GTCAATATAATTTTG[C/T]TGGGACAAGCCACAC | 93664 |
rs73431579 | snp | C/T | 0.118933 | 0.212888 | intron-variant | CADPS2 | GRCh38.p7 | 7:122461132 | AGCCCTTCACAATAG[C/T]AGCCAATTCCTCAAC | 93664 |
rs73431588 | snp | C/G | 0.0944967 | 0.195752 | intron-variant | CADPS2 | GRCh38.p7 | 7:122468692 | TGATTTGTTGAACAT[C/G]GGTCAGTTTGCAAAT | 93664 |
rs73431590 | snp | C/T | 0.0944967 | 0.195752 | intron-variant | CADPS2 | GRCh38.p7 | 7:122468925 | TATATGACACCTCAA[C/T]GCTGAATCAGAGACT | 93664 |
rs73431595 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | CADPS2 | GRCh38.p7 | 7:122470531 | GACAGAGCCTGTTCT[A/G]TTACCTAGGCTGGAG | 93664 |
rs73431597 | snp | A/G | 0.097727 | 0.198275 | intron-variant | CADPS2 | GRCh38.p7 | 7:122473006 | AAAGTCCCAGACCTG[A/G]GAAGCTCCAAAATCC | 93664 |
rs73431600 | snp | A/G | 0.0973687 | 0.197999 | intron-variant | CADPS2 | GRCh38.p7 | 7:122482024 | CCAGAGGCAGACTCT[A/G]TCTAAAAAAATTCTG | 93664 |
rs73431602 | snp | C/T | 0.0966517 | 0.197444 | intron-variant | CADPS2 | GRCh38.p7 | 7:122484804 | TCATTTTATTGTGCT[C/T]TGCAGATGTGTTTTT | 93664 |
rs73433705 | snp | C/T | 0.0948562 | 0.196037 | intron-variant | CADPS2 | GRCh38.p7 | 7:122486634 | AAATGATTTAGGATA[C/T]TACATAAACTTAGTT | 93664 |
rs73433710 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | CADPS2 | GRCh38.p7 | 7:122498303 | AATCTTTGTCATTTT[G/T]CACTTTCATCATGAA | 93664 |
rs73433711 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122499244 | TCTTTTAAGTTCTTT[A/G/T]TAAGATCTCTGTTCC | 93664 |
rs73433715 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | CADPS2 | GRCh38.p7 | 7:122506868 | TAAAAAGAGTTAGTA[C/T]TCGGTGTACAAATTA | 93664 |
rs73433716 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | CADPS2 | GRCh38.p7 | 7:122507233 | AGGCAACATTTGAAC[A/G]GATATCTAAATGGAC | 93664 |
rs73433721 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | CADPS2 | GRCh38.p7 | 7:122511429 | GAGGTGATCATTTGA[C/T]CTCTTAAGACTGATC | 93664 |
rs73433724 | snp | C/T | 0.0952156 | 0.196321 | intron-variant | CADPS2 | GRCh38.p7 | 7:122513502 | CTTATTCTGGGTTCT[C/T]GAAAGGGAATTGATT | 93664 |
rs73433732 | snp | A/G | 0.0718919 | 0.175435 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122533489 | AATCAACAAACTCAC[A/G]CTGCTTAACGGAAGG | 93664 |
rs73433734 | snp | G/T | 0.0908922 | 0.192833 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122534768 | AAAAAAGTGCATTTT[G/T]AATTCCTTTCATTCT | 93664 |
rs73433735 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122535000 | GCTTTGAAAGCTGAG[C/T]ATTTAAAAATATATT | 93664 |
rs73433737 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122538663 | TAAAACCAATTTTGG[A/G]TAAGGAGATAGGAAA | 93664 |
rs73433738 | snp | A/G | 0.0966517 | 0.197444 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539483 | TATGTGGGCAGGAGC[A/G]AAATAAGAGATGGGA | 93664 |
rs73433740 | snp | A/G | 0.0726307 | 0.176182 | intron-variant, nc-transcript-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122543024 | AACACTATCATGTAT[A/G]GTGTTAATATACATT | 93664 |
rs73433742 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122545242 | GTGGGGACAAGATGG[C/T]TTGCAGTTAGCGGAG | 93664 |
rs73433744 | snp | C/T | 0.0722614 | 0.17581 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122551137 | TCTGGTTTAAAAAAA[C/T]AGTCATATTAAAATG | 93664 |
rs73433748 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122553538 | TGCTGCCTACTAAAC[A/C]AAAAAGCAATACAGT | 93664 |
rs73433750 | snp | G/T | 0.0718919 | 0.175435 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554232 | GTTTCAACTATTATT[G/T]TAATTTGAAGAATGT | 93664 |
rs73433754 | snp | A/C | 0.0722614 | 0.17581 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122556818 | CTCAAGAGCTCAGTT[A/C]CTCTTCAATAGGGCT | 93664 |
rs73433759 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122557554 | GGGAGGGAAGATGTC[A/G]TAGGCAGTTACCATG | 93664 |
rs73433764 | snp | C/T | 0.0722614 | 0.17581 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122561914 | GGCTGGAAAGATGGA[C/T]GGATGAATGAATGGG | 93664 |
rs73433769 | snp | G/T | 0.0715223 | 0.175059 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122562761 | TTGCTTACTTTGTGT[G/T]TGCTTATATCTTGCA | 93664 |
rs73433771 | snp | C/T | 0.0722614 | 0.17581 | intron-variant, nc-transcript-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122563364 | TTATAATAATGCTTG[C/T]CATTTATGGAGAATC | 93664 |
rs73433772 | snp | G/T | 0.0715223 | 0.175059 | intron-variant | CADPS2 | GRCh38.p7 | 7:122565119 | TGAAAAATTACTTAC[G/T]CGATATGATGATCAC | 93664 |
rs73433778 | snp | C/T | 0.0722614 | 0.17581 | intron-variant | CADPS2 | GRCh38.p7 | 7:122571995 | CTTAACTCTCACAGA[C/T]AAAATTTATATTGGG | 93664 |
rs73433780 | snp | C/G | 0.0726307 | 0.176182 | intron-variant | CADPS2 | GRCh38.p7 | 7:122572513 | CAAAATTTCTAAAAT[C/G]AAAGAAAAGTTATTT | 93664 |
rs73433782 | snp | A/C | 0.0722614 | 0.17581 | intron-variant | CADPS2 | GRCh38.p7 | 7:122572844 | AAAATCCTTGTTCTG[A/C]CTCCAGGTATTCCCT | 93664 |
rs73433784 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | CADPS2 | GRCh38.p7 | 7:122573413 | GGCATAGTGGCATAC[A/G]ACAGTAGTCCCAGCA | 93664 |
rs73433787 | snp | A/G | 0.0726307 | 0.176182 | intron-variant | CADPS2 | GRCh38.p7 | 7:122578405 | GTGTAAGGAAAGAAT[A/G]ACAGTAGGCAAGGAG | 93664 |
rs73433791 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | CADPS2 | GRCh38.p7 | 7:122588793 | AAATGAGTAAGGACT[A/G]TGTTATTTTCATTGA | 93664 |
rs73433792 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122589900 | AGGTTTGCAATCATT[C/T]ATTGAGGTATAGTTT | 93664 |
rs73433793 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | CADPS2 | GRCh38.p7 | 7:122590399 | GTTCTATAACATGTT[C/T]TTTTATGTAACACTA | 93664 |
rs73433795 | snp | G/T | 0.117537 | 0.212022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122593019 | AAATAAATAAATAAA[G/T]GTATTTGAAATTCCA | 93664 |
rs73433797 | snp | A/G | 0.0905309 | 0.192535 | intron-variant | CADPS2 | GRCh38.p7 | 7:122593569 | CACAGCACATCTCAT[A/G]GAAAGTGCACAGAGA | 93664 |
rs73433800 | snp | C/T | 0.117886 | 0.21224 | intron-variant | CADPS2 | GRCh38.p7 | 7:122595052 | AGAAATTTACCAATA[C/T]GTTATGTTCATATTG | 93664 |
rs73433802 | snp | A/C | 0.0908922 | 0.192833 | intron-variant | CADPS2 | GRCh38.p7 | 7:122596210 | CAAAAATGCTATACA[A/C]ACAGGCTTTTAAGCT | 93664 |
rs73435706 | snp | A/G | 0.0905309 | 0.192535 | intron-variant | CADPS2 | GRCh38.p7 | 7:122600844 | GCAGACAGAGAACAC[A/G]AGAATGAGGCAACCT | 93664 |
rs73435710 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122604499 | GCTCTAGATTTAAGA[A/G]TTGCAGCATCTTAGA | 93664 |
rs73435725 | snp | A/G | 0.0912534 | 0.193131 | intron-variant | CADPS2 | GRCh38.p7 | 7:122614044 | GCCAAGAAAGCAGCT[A/G]TACAAAGATAAGAGG | 93664 |
rs73435731 | snp | A/C | 0.0916144 | 0.193427 | intron-variant | CADPS2 | GRCh38.p7 | 7:122617199 | AGTACTCTGCTTTTC[A/C]AAACAATACTTCCAA | 93664 |
rs73435763 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122642701 | GTTTAGCATCATTGC[C/T]CTCTCTAATATATCT | 93664 |
rs73435765 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122644423 | TAACAACAAAGCAGG[C/T]ACTATCTGATGACAC | 93664 |
rs73435768 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122653132 | TTCCTTCTTGAGTTG[C/T]CAGAGATTGCCTGGC | 93664 |
rs73435782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122664922 | CCCAAGTAGCTGGGA[C/T]CTGCAAACACACACC | 93664 |
rs73437705 | snp | A/G | 0.0104602 | 0.071559 | intron-variant, synonymous-codon | CADPS2, RNF148 | GRCh38.p7 | 7:122702715 | TCCAGATGAAACAGA[A/G]CTATGCGTCGAAGGG | 93664 |
rs73437752 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | CADPS2 | GRCh38.p7 | 7:122770023 | ATAAGATAGGAAGTA[C/T]TAGCTCTGTTTTACA | 93664 |
rs73439722 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122775088 | TATTCAGTTGCTAGG[C/T]TGTTTTGTGTTATAA | 93664 |
rs73441719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122855262 | TCAAATTGTGGACAC[A/G]AAGAAAGGAAGGGAG | 93664 |
rs73441734 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122868136 | AGTTTCTGCATGCAT[C/T]GAGTGCTCCAACTTT | 93664 |
rs73444452 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122372682 | TCACTGTTATTTTCA[C/T]CTACTTTATGTTGAG | 93664 |
rs73444459 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | CADPS2 | GRCh38.p7 | 7:122386596 | AGATTTTTAAGTCTA[C/T]TTCAACCTAAATTTT | 93664 |
rs73444460 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | CADPS2 | GRCh38.p7 | 7:122386785 | CACAACACTTCAGCT[A/G]TTAAAAGCTATATCT | 93664 |
rs73717641 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | CADPS2 | GRCh38.p7 | 7:122368346 | AAAAGGGACACAAGA[A/G]GACTGGAGGTGAAGC | 93664 |
rs73717642 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | CADPS2 | GRCh38.p7 | 7:122380005 | TTCATCAACAAAGGT[G/T]AATAGATGGTAACAA | 93664 |
rs73717643 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | CADPS2 | GRCh38.p7 | 7:122381130 | CCCTCCACAGACACA[C/T]TTACAAAAAAGGCCC | 93664 |
rs73717644 | snp | A/G | 0.110872 | 0.20771 | intron-variant | CADPS2 | GRCh38.p7 | 7:122381633 | CCCATTTTCTTGAAA[A/G]GCAGTGAAAGTCAGT | 93664 |
rs73717645 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122381647 | AAGCAGTGAAAGTCA[A/G]TGGACACTAGGAACC | 93664 |
rs73717646 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122381740 | TAAGCAGAGACAAAG[A/G]GAAAAAGAGGAAGAG | 93664 |
rs73717648 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122405711 | CAGAATGAATGATTC[A/G]CATATGGATAATTGC | 93664 |
rs73717649 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | CADPS2 | GRCh38.p7 | 7:122416760 | GGAAGGCAGAAGTGT[C/T]CTTTGAAGCTGAAGG | 93664 |
rs73717653 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | CADPS2 | GRCh38.p7 | 7:122456224 | TTAGATATAAATAAA[C/T]ATAATAATCCTGCTT | 93664 |
rs73717654 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | CADPS2 | GRCh38.p7 | 7:122462738 | TATCATGCAAAAATC[A/T]TTATTAGTTATGATG | 93664 |
rs73717655 | snp | C/T | 0.081446 | 0.184634 | intron-variant | CADPS2 | GRCh38.p7 | 7:122489101 | AAATAGTTTTCACTA[C/T]ATATAAAAGATATGC | 93664 |
rs73717657 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | CADPS2 | GRCh38.p7 | 7:122515214 | TCATTCCATTATCTG[C/T]GCTTGTGGATGGAAT | 93664 |
rs73717658 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122515475 | CCTCGGGAGCTAGAT[A/G]CTGTGGACATGACAG | 93664 |
rs73717659 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122515628 | TCACTTTGCAGACTG[C/T]TGGGCAACTGGGTCA | 93664 |
rs73717660 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | CADPS2 | GRCh38.p7 | 7:122515665 | AGTGAAAGTAAATAG[G/T]GATACACAAACCATC | 93664 |
rs73717661 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | CADPS2 | GRCh38.p7 | 7:122515751 | AATAATAATCAGCAT[G/T]GCACATGTATATATA | 93664 |
rs73717662 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122516198 | ATCTAGCTGCTATTT[C/T]ACTGGTATGAAAGCA | 93664 |
rs73717663 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122516267 | GAGCCAGATGCAGTG[A/G]CTCATGCCTGTAGTC | 93664 |
rs73717665 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122516869 | ATTCCACAATGTCTA[C/T]ATTGGCCATGTCTTC | 93664 |
rs73717666 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122516990 | ATGTAACCACCACCA[C/T]AATCAACTTATAGAA | 93664 |
rs73717667 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122518507 | TGCTTCATAAAGTAT[G/T]AGTCTACCAAATAAA | 93664 |
rs73717668 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122520044 | GAGTCAACTATTAAT[A/C]AGGTAGCTGGAAGAT | 93664 |
rs73717670 | snp | C/T | 0.165853 | 0.235413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122523663 | AAGTTAATTAATATA[C/T]GCATTACCTCAATAT | 93664 |
rs73717671 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122525905 | TTTGTGTTTCTAAGC[A/G]TATCTAAACATAGGC | 93664 |
rs73717672 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122525919 | CATATCTAAACATAG[A/G]CTACAGTAAAAAAGG | 93664 |
rs73717673 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant, upstream-variant-2KB | CADPS2, LOC105375481 | GRCh38.p7 | 7:122528357 | AAAAACTAGCTCTTC[C/T]TATTCATTAGATAAA | 93664 |
rs73717676 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122544376 | ATTTTGTAAGACAAG[A/C]GTGCACAGTATCTAA | 93664 |
rs73717677 | snp | A/G | 0.093417 | 0.194889 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122549218 | CCTGGGCAACATAGC[A/G]AAACCCTGTCTCTAC | 93664 |
rs73717679 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554267 | TAGAAGGTATCAGTG[A/C]CCTGGTGCCCTGTAT | 93664 |
rs73717680 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122556044 | GTCCTTCCTATAAAG[C/T]CATAGCTGTGTTGAA | 93664 |
rs73717681 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122558298 | AATTAAAATATTTAA[A/C]AGATATAAAAGCTTA | 93664 |
rs73717682 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122558341 | CTGTATCCTAAATTC[A/G]CATTTAAATTAAACT | 93664 |
rs73717683 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122559129 | AATTCTTGAAAAAAT[C/T]ATGACAGCTTTCATA | 93664 |
rs73717684 | snp | A/T | 0.0170251 | 0.090679 | intron-variant, downstream-variant-500B | CADPS2, LOC105375481 | GRCh38.p7 | 7:122564003 | TATCAAATTTTTGGA[A/T]TAGGGATGATCAACC | 93664 |
rs73717685 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122565703 | TTTTTTCCAGCTTTA[C/T]TGAGGTATACTTGAC | 93664 |
rs73717687 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122567720 | GTATAATATTGTAAG[A/G]TTCTTAAATATACAT | 93664 |
rs73717688 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122572249 | TAATTCAACTCTTCA[G/T]ATATAGGAGACTTTT | 93664 |
rs73717689 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122573872 | AAAAATCTCTGCAAT[A/G]ACTGAACCTGCAATT | 93664 |
rs73717695 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122583179 | TATTCAAAAACTATT[A/C]TACAATATTTATCAC | 93664 |
rs73717698 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122583207 | CACCATAGCACATTT[C/G]TCATTTATGCATTAA | 93664 |
rs73717700 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122584136 | GGTTTTATTGCATAA[A/G]TTGAAAAGTGCTATA | 93664 |
rs73717701 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | CADPS2 | GRCh38.p7 | 7:122584323 | TCTTTCTCCTTGAGT[A/G]AATTTTGATAAGCAC | 93664 |
rs73718003 | snp | C/G/T | 0.0337687 | 0.125554 | intron-variant | CADPS2 | GRCh38.p7 | 7:122784219 | TCACTATCTCATCCT[C/G/T]CTCCCTAAGATCTTT | 93664 |
rs73718004 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122786331 | AGGCAGAATTAAGCA[C/T]AGTCAAGACACTGGG | 93664 |
rs73718005 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | CADPS2 | GRCh38.p7 | 7:122786798 | AGACTTATTTGGTCG[C/T]GCTTTGTTCAAAAGA | 93664 |
rs73718007 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | CADPS2 | GRCh38.p7 | 7:122789596 | ACCACACACACTAAC[A/G]AAATAACCACAATAT | 93664 |
rs73718011 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122799280 | TTTCTAGATTGAGAG[A/G]AGACAGAAGCATATT | 93664 |
rs73718013 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122805920 | ATTAGCTCTTCATGG[A/G]TGTTTTAAATATTTT | 93664 |
rs73718015 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122808491 | TCATTACCTTCTGCT[A/G]GAGTGATAAAACATA | 93664 |
rs73718017 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122809872 | CTCTCGTCTTTCCAC[A/G]TGTCAACCTCTAAGC | 93664 |
rs73718019 | snp | A/C | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122823289 | TTAGGGGGAAAAAAT[A/C]TTCCTTTTGCCTTGG | 93664 |
rs73718020 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122823964 | AGAGCTCCATTTCCA[C/T]ACTCCAATCTTCCAA | 93664 |
rs73718021 | snp | C/G | 0.0333695 | 0.124785 | intron-variant | CADPS2 | GRCh38.p7 | 7:122826273 | CTTCTACCTCCATTT[C/G]GACTTAAGAAGGCAG | 93664 |
rs73718022 | snp | C/G | 0.0314385 | 0.121371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122829436 | TTTACAAGGAGAAAT[C/G]AGTCTTATATATAGG | 93664 |
rs73718023 | snp | A/C/G | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122831885 | TCTGTCTTTAAAAAG[A/C/G]GAAGCACCAATCTAG | 93664 |
rs73718024 | snp | A/G/T | 0.0379877 | 0.132479 | intron-variant | CADPS2 | GRCh38.p7 | 7:122833257 | GTTTGCGCTGTTTTA[A/G/T]GTACTACTAAAATTG | 93664 |
rs73718026 | snp | A/C | 0.0314385 | 0.121371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122842195 | GAATGAACATTTTGA[A/C]TTCTCTTTCCTCCCT | 93664 |
rs73718027 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122844161 | AGCCTCACCTGGAGG[C/T]GAGACTGAAGTTACA | 93664 |
rs73718028 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | CADPS2 | GRCh38.p7 | 7:122850430 | CTCCCAAAGCACTTA[C/T]GGATTCTTCTGAGGT | 93664 |
rs73718030 | snp | A/T | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122852378 | CTCATGCAGCTTACA[A/T]TTATGTGTGTCAAGG | 93664 |
rs73718032 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122854916 | TAAAAGGACATCACT[A/G]TATTTGTGTAAGACC | 93664 |
rs73718044 | snp | G/T | 0.0325976 | 0.123435 | intron-variant | CADPS2 | GRCh38.p7 | 7:122870954 | GAAGATATAGTCCAG[G/T]TCAGACACTGAACTA | 93664 |
rs73718047 | snp | C/G | 0.0279526 | 0.114869 | intron-variant | CADPS2 | GRCh38.p7 | 7:122884829 | ATGTCAATTATACCT[C/G]AAAAAATAAAGGTTA | 93664 |
rs73719703 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122584405 | AGTTGTAAATTTTTT[C/G]ATCTTTGAATCCTTA | 93664 |
rs73719705 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122585477 | AAAAAAAAAAAAAAA[A/G]GGCAGGAAAAGAGGA | 93664 |
rs73719707 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122586204 | AAAAATGGAGTACCT[G/T]TTATGTGGAGATGAC | 93664 |
rs73719708 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122588588 | ATTCTTCTAATAATA[C/G]AATAAAAGTTTTGGT | 93664 |
rs73719709 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | CADPS2 | GRCh38.p7 | 7:122593316 | TTGTGGAAAAAAGAC[C/G]GATTAAATAACAAAA | 93664 |
rs73719711 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122595065 | TATGTTATGTTCATA[A/T]TGCTCCCAAACCCTC | 93664 |
rs73719713 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122595355 | GATATCTTCCCCTAA[C/T]TGATGTCTAATTCGA | 93664 |
rs73719714 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122596714 | ATTCAAGACAGAAGA[C/T]AATGATGTGCAGAAA | 93664 |
rs73719715 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122600965 | ATGTTGACATTTAGC[C/T]ACTGATTTTAACAAA | 93664 |
rs73719716 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122601031 | TGTGGATAATGATAG[A/G]TTAAGTTTTTACATC | 93664 |
rs73719717 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | CADPS2 | GRCh38.p7 | 7:122603143 | CTTTTCCCTTCATAA[C/T]TGACAATTAGGCATT | 93664 |
rs73719718 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122606973 | CTGCTAAGAATTCAT[C/T]GGAGAAGAGTTACAT | 93664 |
rs73719719 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | CADPS2 | GRCh38.p7 | 7:122611509 | CAATTACTTTTGCAC[C/T]AACATAACAGGAAAA | 93664 |
rs73719721 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | CADPS2 | GRCh38.p7 | 7:122616382 | TGATAAGAATTTTGA[A/T]CCAAAAGGGCTCAAA | 93664 |
rs73719723 | snp | A/T | 0.0689305 | 0.172377 | intron-variant, upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122622623 | GCTCTTTCTTTAATG[A/T]TTGCCAACCTGGCAC | 93664 |
rs73719724 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | CADPS2 | GRCh38.p7 | 7:122627545 | GTTCATCACTAACCC[C/T]TTCTTCTGACTCAGC | 93664 |
rs73719726 | snp | A/T | 0.0711525 | 0.174681 | intron-variant | CADPS2 | GRCh38.p7 | 7:122638354 | GGGCTCTGCCCAAGT[A/T]AGGAGCAGGGTGAAG | 93664 |
rs73719728 | snp | A/G | 0.0711525 | 0.174681 | intron-variant | CADPS2 | GRCh38.p7 | 7:122648919 | AGAGATTACCTGAAG[A/G]GCTAATATGTAGTTC | 93664 |
rs73719729 | snp | A/T | 0.0715223 | 0.175059 | intron-variant | CADPS2 | GRCh38.p7 | 7:122650883 | TTTATTTACCAAAAA[A/T]TTAACACATATATAA | 93664 |
rs73719731 | snp | A/C | 0.0696718 | 0.173152 | intron-variant | CADPS2 | GRCh38.p7 | 7:122662103 | ACCAATGCAAAGTAA[A/C]CAATATGGATATAAC | 93664 |
rs73719733 | snp | A/G | 0.0696718 | 0.173152 | intron-variant | CADPS2 | GRCh38.p7 | 7:122663998 | GACACCAAATTGGCT[A/G]ACACCCTGATTTTGG | 93664 |
rs73719738 | snp | C/T | 0.0908922 | 0.192833 | intron-variant | CADPS2 | GRCh38.p7 | 7:122670233 | GCTTAAAATTTTTCA[C/T]TGGTCTTCCACCAAA | 93664 |
rs73719740 | snp | C/T | 0.0861826 | 0.188849 | intron-variant | CADPS2 | GRCh38.p7 | 7:122678482 | AAGGCTTGGAGTTTA[C/T]GTTTTTTGTAAGGAT | 93664 |
rs73719742 | snp | A/G | 0.0970103 | 0.197722 | intron-variant | CADPS2 | GRCh38.p7 | 7:122681724 | AATAAAATGGAAATT[A/G]TAAAAAAATAATAAT | 93664 |
rs73719745 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | CADPS2 | GRCh38.p7 | 7:122696019 | GTGCAGGGACTGCCA[A/G]CACTACAGATGCATT | 93664 |
rs73719746 | snp | C/T | 0.0908922 | 0.192833 | intron-variant | CADPS2 | GRCh38.p7 | 7:122696588 | ACACTGAGCAACTCA[C/T]AAGATTCCTCTTCAC | 93664 |
rs73719749 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122707504 | GCACTGCTCAGATAG[C/T]ATCTTTAAGATGAAA | 93664 |
rs73719750 | snp | A/G | 0.0836354 | 0.186609 | intron-variant | CADPS2 | GRCh38.p7 | 7:122711057 | ACTTTTTTAAAGAAA[A/G]AGAACAGGCAATGAT | 93664 |
rs73719751 | snp | C/T | 0.0948562 | 0.196037 | intron-variant | CADPS2 | GRCh38.p7 | 7:122711114 | TTACATTGACAACAG[C/T]TGTCCAGAAAAAGGC | 93664 |
rs73719752 | snp | C/T | 0.0948562 | 0.196037 | intron-variant | CADPS2 | GRCh38.p7 | 7:122716543 | GTAGGGTCGGGGGAG[C/T]GGGGAGGGATAGCAT | 93664 |
rs73719754 | snp | C/T | 0.0948562 | 0.196037 | intron-variant | CADPS2 | GRCh38.p7 | 7:122720241 | ACAATACCATTTAAT[C/T]ACACTTTTAGTTATA | 93664 |
rs73719756 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | CADPS2 | GRCh38.p7 | 7:122725841 | ATACTCTAATCCATA[C/T]TGAAACAGGAAGTAC | 93664 |
rs73719761 | snp | C/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122746642 | AGACACACACACACA[C/G]ACACACACACACACA | 93664 |
rs73719762 | snp | G/T | 0.0337553 | 0.125452 | intron-variant | CADPS2 | GRCh38.p7 | 7:122746743 | CTGTGGGCCAGACAA[G/T]CTTGCTCTATCACTA | 93664 |
rs73719765 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | CADPS2 | GRCh38.p7 | 7:122755995 | CTTTTATGTGAAAAG[C/T]GGGATCAGAACATCA | 93664 |
rs73719766 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | CADPS2 | GRCh38.p7 | 7:122758932 | ATAATTAAAGCATAC[A/G]TTTGTTTAGAAGAAA | 93664 |
rs73719767 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122759714 | AGGAATCCAAAATTT[C/T]TTCTTGCCCAGACCT | 93664 |
rs73719769 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | CADPS2 | GRCh38.p7 | 7:122767290 | TACAACTGTGAGGTC[A/G]ATGTTATTATTCCTA | 93664 |
rs73719770 | snp | A/C | 0.0349115 | 0.127424 | intron-variant | CADPS2 | GRCh38.p7 | 7:122769438 | ATTCCTTCACTCCAC[A/C]TCTTTGTGTTCATTC | 93664 |
rs73719772 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | CADPS2 | GRCh38.p7 | 7:122772800 | CAGATCCAGTAACTA[C/T]AACAGACTATGCCTA | 93664 |
rs73719773 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122774310 | CACACACACACACAC[A/T]CTCTGGAAACAAAAG | 93664 |
rs73719774 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | CADPS2 | GRCh38.p7 | 7:122775158 | TCTTTTATCCAATGG[C/T]GATATTAAAAACATT | 93664 |
rs74221978 | in-del | -/TA/TATA | 0.252983 | 0.249982 | intron-variant | CADPS2 | GRCh38.p7 | 7:122645592 | ATCTTAGTGTGTGTG[-/TA/TATA]TATATATATATATAA | 93664 |
rs74302567 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122731683 | AGAGGGGRAAAAAAA[A/C]CCCTTCAATTAACAA | 93664 |
rs74327836 | snp | A/T | 0.0100929 | 0.0703178 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698876 | TCATAAGCCAGGAAG[A/T]GGCAGTGTTGTTTCT | 93664 |
rs74331865 | snp | G/T | 0.031825 | 0.122064 | intron-variant | CADPS2 | GRCh38.p7 | 7:122436954 | TGATTCTTACAGGTT[G/T]TTTTGGGTAGAGTAC | 93664 |
rs74332831 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | CADPS2 | GRCh38.p7 | 7:122623931 | AAAAATAATCTATTT[A/G]TATTTAGCTTTAACT | 93664 |
rs74334988 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122608719 | ATGCTTTTAATAAAA[C/T]AGCACTATGGGATGA | 93664 |
rs74362107 | snp | C/T | 0.123105 | 0.215401 | intron-variant | CADPS2 | GRCh38.p7 | 7:122468037 | TTATTTCTGAAACAC[C/T]CAGAGTGCTATTCAG | 93664 |
rs74366932 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122552270 | ATTTTCAGTTCTAAC[A/G]TTGCTTCAATGTATA | 93664 |
rs74367820 | snp | A/G | 0.2462 | 0.249971 | intron-variant | CADPS2 | GRCh38.p7 | 7:122673741 | GGACTCAGGGGCCCA[A/G]CTGGCTTCGCCTAGT | 93664 |
rs74376420 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122383590 | TGTGCCTGCTTTCCC[A/G]CAGGTGATTCTGAAC | 93664 |
rs74384170 | snp | A/T | 0.116138 | 0.211142 | intron-variant | CADPS2 | GRCh38.p7 | 7:122413695 | AATGCAGTCCACCAA[A/T]TCACTCTGGAAGTCA | 93664 |
rs74403681 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | CADPS2 | GRCh38.p7 | 7:122749869 | AAATACATGCTTCAG[A/G]TTTTTAATTCTAAAA | 93664 |
rs74405430 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539200 | ACCTTTAAGATCACA[A/G]AGGACTCTGCCCTCA | 93664 |
rs74408034 | snp | A/T | 0.177824 | 0.239355 | intron-variant | CADPS2 | GRCh38.p7 | 7:122519701 | AAATCCAGCTATCCT[A/T]AGGTCACACTGTATC | 93664 |
rs74410468 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122378515 | CATGTTCATGGGGCA[G/T]CTCTATTTTTTCTTT | 93664 |
rs74423868 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122845790 | GGGGCTACAAGCAAC[A/G]GGAAAACTTGATAAA | 93664 |
rs74426975 | in-del | -/AA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122477555 | CACCAAAAAAAAAAA[-/AA]CAAAAAACAAAAAAC | 93664 |
rs74433894 | snp | A/C | 0.0644693 | 0.167566 | intron-variant | CADPS2 | GRCh38.p7 | 7:122490389 | TTGATATTAGCAGTT[A/C]AATGTTTTAAAGAAT | 93664 |
rs74440070 | snp | C/G | 0.0629771 | 0.165899 | intron-variant | CADPS2 | GRCh38.p7 | 7:122511857 | TATTAAAATTGCTTA[C/G]GAAACACATTTTAAT | 93664 |
rs74442528 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | CADPS2 | GRCh38.p7 | 7:122446693 | CATTTGCAAATAGCT[A/G]TAGCTCTCTCCTCTC | 93664 |
rs74456609 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | CADPS2 | GRCh38.p7 | 7:122724274 | GGACCTTGCCTTGTT[C/T]ATCTTTTTATTTCCA | 93664 |
rs74465475 | snp | A/G | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122749975 | TTAAAAAAAAAAAAA[A/G]AGAAAAAGAGAGAGT | 93664 |
rs74468974 | snp | A/G | 0.219648 | 0.248151 | intron-variant | CADPS2 | GRCh38.p7 | 7:122639698 | TTTTAATAATGATGT[A/G]CCCCATTTTACAAAA | 93664 |
rs74469470 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | CADPS2 | GRCh38.p7 | 7:122395209 | ATATGTTACTTTATG[C/T]GTTTCTGAAATTTCT | 93664 |
rs74477971 | snp | C/T | 0.294064 | 0.246086 | intron-variant | CADPS2 | GRCh38.p7 | 7:122715380 | TTTCTCCTTCCAGAA[C/T]GCAGATGGCAAAGTG | 93664 |
rs74478837 | snp | A/T | 0.195526 | 0.243993 | intron-variant | CADPS2 | GRCh38.p7 | 7:122355655 | ATCCAGAAAATTTTT[A/T]CTAGCTCTTTATCTT | 93664 |
rs74485694 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122710063 | ATAAAAAAAAAAAAA[A/T]AATGACCTTCTGCCA | 93664 |
rs74508717 | snp | A/C | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122800994 | GAGACTCTGCCTCAA[A/C]AAAAAAAAAAAAAAG | 93664 |
rs74511743 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122414562 | CCTAGAAAAGAACCT[C/T]CTGGGAATTCATTTC | 93664 |
rs74522435 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | CADPS2 | GRCh38.p7 | 7:122667214 | CACCTTTGAGAAATT[C/T]AGTAATGTATGTATA | 93664 |
rs74524053 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | CADPS2 | GRCh38.p7 | 7:122734675 | AATGAAAGGCATTTT[A/G]GGAAAAAAATTGAGA | 93664 |
rs74525764 | snp | A/C | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122380113 | GCCTTTAAATAAATA[A/C]CAAAAAAAGATGTAT | 93664 |
rs74535115 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | CADPS2 | GRCh38.p7 | 7:122659724 | CGAATTGCAGAAAAA[C/T]GAAAGAAGGAAAAAC | 93664 |
rs74537592 | snp | A/G | 0.42644 | 0.177113 | intron-variant | CADPS2 | GRCh38.p7 | 7:122822388 | CCTCCCTTCAGCTTA[A/G]TCTCTCCCACTCTAG | 93664 |
rs74538319 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122405575 | GGCTGAGGCATGAGA[A/G]TCGCTTGAACTTCGG | 93664 |
rs74548409 | snp | A/G | 0.000198847 | 0.00996914 | intron-variant | CADPS2 | GRCh38.p7 | 7:122386289 | AGAAAAAAAAATGAG[A/G]CTTACCCATTGACTA | 93664 |
rs74551759 | snp | C/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122332396 | CTTTCTTCATCATCT[C/T]TTTTTTTTTTTTTTC | 93664 |
rs74558095 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | CADPS2 | GRCh38.p7 | 7:122834182 | TGGTAGAAGGTAATA[C/T]GGTAGAAAGTAAGAA | 93664 |
rs74569196 | snp | G/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122560590 | AAATCATGGTTCAAT[G/T]TTTGATTAAAAATCA | 93664 |
rs74569799 | snp | A/T | 0.0535932 | 0.154675 | intron-variant | CADPS2 | GRCh38.p7 | 7:122456688 | GCCACTGAGGCCTGA[A/T]CTTAACGTCTGCCTG | 93664 |
rs74623793 | snp | C/T | 0.040671 | 0.13668 | intron-variant | CADPS2 | GRCh38.p7 | 7:122392665 | GTACCAACTATATAA[C/T]AAAAGAACAAAAGAA | 93664 |
rs74625172 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122523292 | ATGCACTGTCACCTA[G/T]AAATAAAACAACTAG | 93664 |
rs74630632 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | CADPS2 | GRCh38.p7 | 7:122739614 | TCAATATTTTTATGA[A/G]TAGAGGATACTGCAG | 93664 |
rs74633956 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122406172 | TGTGATTTCCCCCCC[-/C]ACCAGTTTTATCACA | 93664 |
rs74641993 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122601588 | TAGGATCATCTTCTC[A/T]TCCTTAAAAAAACAT | 93664 |
rs74651864 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122841711 | ACACCATTAAATAAC[C/T]AAAGAAAACGAAGAG | 93664 |
rs74654778 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122454908 | GCTTATCCCTGAGTA[C/T]GCAGGCAGCCTCTTG | 93664 |
rs74669205 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | CADPS2 | GRCh38.p7 | 7:122486685 | TTAGAGGATTGACTC[C/T]AATTTTCAAAGAAGT | 93664 |
rs74690652 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122735326 | CTACAGGCTAAACAC[C/T]CCCAGCTCCTTCAAC | 93664 |
rs74691758 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122677924 | CTTGATGGTATTTCT[C/T]TATTCTAAGCCATCT | 93664 |
rs74696979 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122854582 | CTAGCTGTGCCAGAA[A/C]AAGGTGTGCTGCACA | 93664 |
rs74698384 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | CADPS2 | GRCh38.p7 | 7:122612690 | ATCTTTACAAAAGTT[A/G]ATAAACTCTTCCTAA | 93664 |
rs74702578 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | CADPS2 | GRCh38.p7 | 7:122488271 | AAAAAAGTTCTACCC[A/G]GGGTTGAGGGAGTCT | 93664 |
rs74713327 | snp | C/T | 0.097727 | 0.198275 | intron-variant | CADPS2 | GRCh38.p7 | 7:122884783 | TGAAACCACCAATAG[C/T]TAGGGTGGAGTGGTA | 93664 |
rs74731972 | snp | C/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122525954 | AATCTTATGGGATCA[C/G]TGTCATATATGCCAT | 93664 |
rs74737271 | snp | G/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122862725 | ATAAGCTCCATTTTG[G/T]TTTTTTTAAAAAAAA | 93664 |
rs74738785 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122595173 | ACCAAAAAAAAAAAA[A/G/T]TCCTTTCAAATGTAA | 93664 |
rs74738804 | snp | C/G | 0.0633504 | 0.166319 | intron-variant | CADPS2 | GRCh38.p7 | 7:122346783 | TACTAGTAAGGGATA[C/G]ATGCCTGCATGGCTG | 93664 |
rs74744590 | snp | C/G | | | missense | CADPS2 | GRCh38.p7 | 7:122320242 | AAACAGAGGCTGTGG[C/G]CTCCTCTACTGTTAA | 93664 |
rs74753588 | snp | A/G | 0.195214 | 0.243923 | intron-variant | CADPS2 | GRCh38.p7 | 7:122357310 | AAACTTTATCAACCA[A/G]AGTACAATGCTTATT | 93664 |
rs74769178 | snp | A/G | 0.089084 | 0.191327 | intron-variant | CADPS2 | GRCh38.p7 | 7:122374161 | AAAATCACCAAGATC[A/G]TCTCCATAGATGCAG | 93664 |
rs74776278 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | CADPS2 | GRCh38.p7 | 7:122725553 | CTCACTTCCCTCCCC[C/T]CACCCTCTCATTTTG | 93664 |
rs74784655 | snp | G/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122575190 | AAGTAAAAAAAAAAG[G/T]TGGTGGGAGCATCTA | 93664 |
rs74795009 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122552739 | AGTACTGGCCATGGG[C/T]AAATTAGGGTCATCT | 93664 |
rs74795683 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122731675 | AAAGGTGAAGAGGGG[A/G]AAAAAAAMCCCTTCA | 93664 |
rs74799007 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122768967 | ATCAGAAAAAAAAAA[A/G]GAAAGAAACGGTCAC | 93664 |
rs74823805 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | CADPS2 | GRCh38.p7 | 7:122507097 | AATAATAATAAACAT[A/G]TAAATGTAAAAAAAA | 93664 |
rs74830437 | snp | C/T | 0.190519 | 0.242821 | intron-variant | CADPS2 | GRCh38.p7 | 7:122616070 | CCAATCTTAAAACAC[C/T]GTAACCTATCATTCT | 93664 |
rs74835685 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | CADPS2 | GRCh38.p7 | 7:122515192 | CAGCATTTATGATAC[C/T]GTTAATTCATTCCAT | 93664 |
rs74847837 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | CADPS2 | GRCh38.p7 | 7:122634585 | CTAGCTAGCAGTCTA[C/T]CAATCCTGTTTATGT | 93664 |
rs74848754 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122373786 | CAAAAGTGAATTCTA[C/T]CAAACATTTAAAGAA | 93664 |
rs74851730 | snp | G/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122448612 | TGTAGTTGTAGTTTT[G/T]GGGTGGTAGTGTGGG | 93664 |
rs74852775 | snp | A/C | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122750893 | CTGGAGATGGTAATT[A/C]TGAGTTAAGAAATCT | 93664 |
rs74861320 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | CADPS2 | GRCh38.p7 | 7:122599635 | TGCCTAGTGTTAATC[C/T]GGATAACTAAAAAGC | 93664 |
rs74890124 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | CADPS2 | GRCh38.p7 | 7:122503768 | ATTTATCATGCATCT[A/G]CAGTGAATTTTTCCA | 93664 |
rs74890846 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | CADPS2 | GRCh38.p7 | 7:122392260 | TATAAATTATAATGA[C/T]GATGCCTGATGATAG | 93664 |
rs74891352 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | CADPS2 | GRCh38.p7 | 7:122693617 | TCTCCAGGTGATTCC[A/G]ATGTGCAGCCAAGGT | 93664 |
rs74915988 | snp | G/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122463337 | AGATTTTTTTTTTTT[G/T]GAGGTGGAGTCTCGC | 93664 |
rs74923167 | snp | A/G/T | 0.0150606 | 0.0854603 | intron-variant | CADPS2 | GRCh38.p7 | 7:122749198 | CACTGAAGAATTGAT[A/G/T]CAAGTGTGCATTCCT | 93664 |
rs74924390 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CADPS2 | GRCh38.p7 | 7:122477726 | GATACATATAGACAG[C/T]AAAATGGTTACAATA | 93664 |
rs74933660 | snp | C/T | 0.0941369 | 0.195465 | intron-variant | CADPS2 | GRCh38.p7 | 7:122342203 | TGGAGATGGGAATGA[C/T]AGCAGCAGTGCAGAA | 93664 |
rs74953678 | snp | C/T | 0.136506 | 0.222754 | intron-variant | CADPS2 | GRCh38.p7 | 7:122355205 | TATGTTCTAGGAACA[C/T]GAATTCCTCCTTTTC | 93664 |
rs74956897 | snp | C/G | 0.441359 | 0.160878 | intron-variant | CADPS2 | GRCh38.p7 | 7:122822463 | CATCGCCCATTCTCT[C/G]TCCATATCACCCCCC | 93664 |
rs75017925 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | CADPS2 | GRCh38.p7 | 7:122636614 | GGGATTACAGGTGCA[C/T]ATCACCATGCCAAGC | 93664 |
rs75018653 | snp | C/G/T | 0.0217236 | 0.101931 | intron-variant | CADPS2 | GRCh38.p7 | 7:122600574 | TTAATGAGTTTGCCA[C/G/T]AGCAGAAATCAAGAC | 93664 |
rs75026306 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122805167 | ATCATTATTATTATT[A/G]TTATTGTTATTGAGA | 93664 |
rs75026593 | snp | A/C | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122580452 | AGCAAGATTCTGTCT[A/C]AAAAAAAAAAAAAAA | 93664 |
rs75047633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122651660 | GGGATAAGTGAACAA[A/G]ATCTCAGTTAACTTT | 93664 |
rs75053906 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122562883 | TACAATAAACTGAAA[A/C]ATTTTTTTAAAGGTT | 93664 |
rs75055928 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122868619 | ACTCCAACAAGACAG[A/G]AAGGGGTGGTTCTCT | 93664 |
rs75060895 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122625726 | GCCAGTGCCCACAGC[C/G]GTGGGAGCCAATTCC | 93664 |
rs75081084 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | CADPS2 | GRCh38.p7 | 7:122848437 | TATCTACAGGCTACC[A/G]TGGCCAGGTCTAGGC | 93664 |
rs75083530 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122801567 | ACACATGTTCCCATT[A/T]GATCAGGAAAAAGAC | 93664 |
rs75087552 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122706714 | ACATATTCCTTGCTC[A/T]TATATATGTATATAT | 93664 |
rs75090884 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | CADPS2 | GRCh38.p7 | 7:122852802 | ACCCACTGGAGGTCA[A/T]GAACAGAGAAGCAAT | 93664 |
rs75121911 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122646804 | TAAAAACAAAAGTAT[A/G]TAGGATTAGAAGGAG | 93664 |
rs75122564 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122847936 | GCCAGTAAAACATCA[C/T]CCTATATGAAAACAG | 93664 |
rs75139000 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122523224 | TTCTCCATATCTTCT[C/T]CAGCATTTTACAATT | 93664 |
rs75141015 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122859434 | CTCCAGTCAATTGTG[C/T]ATTTCATCATATCAA | 93664 |
rs75144481 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | CADPS2 | GRCh38.p7 | 7:122720794 | CACACATAGAAACAA[C/T]GATGAGAGTTAACAA | 93664 |
rs75144980 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122653466 | CCTTTCTATAAAGAA[C/G]AGGCTAGTTTCTGTG | 93664 |
rs75151228 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122493749 | TTTTTGCCAATTTTG[A/T]TGAGTGGGAAATACT | 93664 |
rs75154494 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | CADPS2 | GRCh38.p7 | 7:122465421 | GCTGTGGACTGGTAC[C/T]AATCCATGGCCTGTT | 93664 |
rs75163947 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122522576 | GGGAACATTTCAAAT[A/C]TTCTCTTCTAGCTAT | 93664 |
rs75166043 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122883325 | GTGATTAATTTTCTT[C/G]ATAAAATGAGGACCC | 93664 |
rs75174874 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122366117 | TTTTTTTTTTGTTAA[G/T]ATCAGGACTAACTAG | 93664 |
rs75183110 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122737177 | CATCTAGAATTAACT[G/T]TATAGTAAAGAAAAA | 93664 |
rs75188105 | snp | G/T | 0.45198 | 0.147323 | intron-variant | CADPS2 | GRCh38.p7 | 7:122497206 | TTCAGTCTCAATTAT[G/T]CTGTGTTATATTTTA | 93664 |
rs75192238 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | CADPS2 | GRCh38.p7 | 7:122861739 | TAATTGCTCAGATTC[A/G]ATCATTACGCACTAT | 93664 |
rs75192306 | snp | A/C | 0.277778 | 0.248452 | intron-variant | CADPS2 | GRCh38.p7 | 7:122793435 | GGCTGTTTTGTCTGA[A/C]ATTAGAATAGCAACC | 93664 |
rs75195780 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122839224 | GAAAACTGGCTAGCC[A/T]TATGTAGACAGCTGA | 93664 |
rs75199043 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122585479 | AAAAAAAAAAAAAAG[A/G]CAGGAAAAGAGGAAA | 93664 |
rs75200195 | snp | A/C | 0.0803491 | 0.183626 | intron-variant | CADPS2 | GRCh38.p7 | 7:122624295 | CAAGTCATGTGTTCT[A/C]ATTAGGTCCTCTGTA | 93664 |
rs75210559 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | CADPS2 | GRCh38.p7 | 7:122881605 | AAGGAGCACAAAAAA[A/G]TGAATCACCCTATCT | 93664 |
rs75215932 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122533105 | CTCAAATCTCTTTTA[C/G]CTCTTAAATTCCTAC | 93664 |
rs75216966 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122713584 | AACCATTTTTTTCAA[C/T]CTTAACAATTGTAAG | 93664 |
rs75228373 | snp | G/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122448615 | AGTTGTAGTTTTTGG[G/T]TGGTAGTGTGGGGAA | 93664 |
rs75231173 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | CADPS2 | GRCh38.p7 | 7:122516921 | ATTGGTATAGTTTAC[A/G]TAAAGTAAAATTACC | 93664 |
rs75231275 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122615375 | AACAGCAGCATGAAC[C/T]GTAATAAGGAAGATT | 93664 |
rs75244322 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122835546 | CTTGAAAAAAGATTA[A/G]ACGAACGGATAACTA | 93664 |
rs75248755 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122416295 | GAATACATTATTTAG[A/T]CAAAAAAAAAAAAAC | 93664 |
rs75253466 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122638869 | CCTGAATCCTGACGT[A/G]GTTTCTTAGATGATC | 93664 |
rs75258752 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122775974 | TATTCAAGTTCAAAA[A/T]TTTTTTTCTAGAGAA | 93664 |
rs75299245 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | CADPS2 | GRCh38.p7 | 7:122525655 | TGCATCATGAGGCAA[A/T]TTTGTCTTTGTGAGA | 93664 |
rs75301916 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122579347 | TGCTCAAAACATCAA[C/T]AGTGCTAAGGTTGGG | 93664 |
rs75313853 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | CADPS2 | GRCh38.p7 | 7:122825976 | CGCCAAGTAGCAAGC[G/T]ACAACTATGGTGCAC | 93664 |
rs75322502 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122700981 | TGGAAACTAGATTTC[C/T]TGGGTATTAATAAAA | 93664 |
rs75330139 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122401552 | AATAGTGTGCAAGGG[C/T]AGAATCTATTTGTAC | 93664 |
rs75346679 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122415827 | AATTATACACACACA[A/C]AATTGCTTTGTAATA | 93664 |
rs75356127 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122362191 | ACACAATGGCTGACA[C/T]TAGTTAACAAGCATT | 93664 |
rs75381519 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | CADPS2 | GRCh38.p7 | 7:122750390 | AAATTCAAATATAAT[A/G]GGCAACCTATATTTG | 93664 |
rs75390883 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122804002 | AAAAAAAAAAAACAC[A/T]GCAAAGCACACTCTG | 93664 |
rs75396994 | snp | A/C | 0.0225045 | 0.103662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122864523 | TTATGTCACATGGCC[A/C]CTTGTAGCTCTCAGG | 93664 |
rs75457467 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122834421 | TTCATCTCACTGAGG[C/T]GTGTCAAACAGTGGG | 93664 |
rs75461149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122343345 | TTACTTTTAGACCCA[C/T]AGCCATGTCAGATGC | 93664 |
rs75461294 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant, utr-variant-5-prime | CADPS2, RNF148 | GRCh38.p7 | 7:122702836 | AGATAGCTTGTTGGC[A/G]GCAGATTACTAAAGC | 93664 |
rs75462212 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | CADPS2 | GRCh38.p7 | 7:122616943 | TAATAACTTCTTAAT[A/C]ATAAAAATGTTTGAT | 93664 |
rs75482182 | snp | C/G | 0.16028 | 0.233346 | intron-variant | CADPS2 | GRCh38.p7 | 7:122644157 | ACTATGAATAAGAGA[C/G]AATGACCACCAAACA | 93664 |
rs75486808 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122770743 | CCTGCATTATAGATG[A/G]CGGCACCCACAGGGC | 93664 |
rs75491071 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122533089 | GTGGGGCTAAGTAAC[A/C]CTCAAATCTCTTTTA | 93664 |
rs75492699 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | CADPS2 | GRCh38.p7 | 7:122501330 | AAGGATTTGAAGATA[C/T]TACATTTGGAAATTT | 93664 |
rs75496195 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122349094 | TGTGGGGTTTTTTTT[G/T]GTGTGTACATGAAGA | 93664 |
rs75498466 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | CADPS2 | GRCh38.p7 | 7:122354317 | AGGTGTAATTACATC[C/T]CCATTTTACAGAAGA | 93664 |
rs75520353 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122826299 | GGCAGTGTTCTCCTT[C/T]CTCATGGAAAATGCT | 93664 |
rs75533243 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122725122 | GATATGAAAATATAT[A/G]TGTTTCTTTTGGTGA | 93664 |
rs75539298 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | CADPS2 | GRCh38.p7 | 7:122806916 | CATGTGACAACTATC[A/C]ATCTATTGCCTCTTA | 93664 |
rs75545320 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122348984 | GTGGTAAAATTTACA[A/C]ACCGAAAGTCACTGC | 93664 |
rs75549741 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122530412 | AGTAAAATGAGACTA[C/T]GTTACATTAGGAAAT | 93664 |
rs75550702 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122395102 | ACATTATCTTCTTCA[A/G]AGCAAAAACATCCCA | 93664 |
rs75558169 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122374364 | GCCCACACTTACCAC[C/T]TCTATTCAACATAGT | 93664 |
rs75567480 | snp | A/G | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122337774 | AAAAAAAAAAAAAAA[A/G]GCTGAGGAGCAGCTC | 93664 |
rs75576229 | in-del | -/AA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122630389 | AGTCAAAAAAAAAAA[-/AA]GAGGAAGATGTTCCT | 93664 |
rs75577025 | snp | C/T | 0.204803 | 0.245881 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122559994 | ATGGGGATCAAGAGG[C/T]TGCACATTGTTGGGT | 93664 |
rs75590378 | snp | C/T | 0.235564 | 0.249583 | intron-variant | CADPS2 | GRCh38.p7 | 7:122689233 | AACCTCCTGGGACAC[C/T]CCTTGTAAAGCTGCC | 93664 |
rs75597889 | snp | C/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122688126 | ATTCTTAACTCTTCA[C/G]TCTTCCTCTACTCCC | 93664 |
rs75625328 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | CADPS2 | GRCh38.p7 | 7:122671480 | ATGCCTGAAATCGCA[C/G]CACTTTGGGAGGCCA | 93664 |
rs75628888 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122665153 | TACTCCCAAGTTATG[A/C]TCATACTACTTGCAC | 93664 |
rs75643376 | snp | A/G | 0.0414363 | 0.137845 | utr-variant-3-prime | CADPS2 | GRCh38.p7 | 7:122319877 | TAAAAAAAAAAGTTC[A/G]TGTTCTGATCACAAG | 93664 |
rs75646026 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122520345 | GTTGAATGTGTGTGT[G/T]TTTTTTTTAAGTAGA | 93664 |
rs75647344 | snp | G/T | 0.0626037 | 0.165477 | intron-variant | CADPS2 | GRCh38.p7 | 7:122396399 | CAATAATAACCTAAC[G/T]GGTCTTTAGGATCCT | 93664 |
rs75648327 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122767337 | ACATTTCAGAAGTTA[A/G]AGAAACTGCCCATGC | 93664 |
rs75654129 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122831739 | TTTACTCTGAGTGCT[G/T]TAAGAGGGGACCATA | 93664 |
rs75658445 | snp | A/C | 0.0663309 | 0.169604 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122540831 | ATTTGTGCTCTGTAT[A/C]ACAAAGTTCCAGTTT | 93664 |
rs75683032 | snp | C/T | 0.0108506 | 0.072853 | intron-variant | CADPS2 | GRCh38.p7 | 7:122393334 | TAAAGAAACAAACAA[C/T]GTGGGAAGGGACCAC | 93664 |
rs75689289 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122860586 | TTTTAGAACCCCCAA[A/G]GATAAAGAACATTAA | 93664 |
rs75704010 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122400832 | TTAAGCACTTGAAAG[A/G]GAATAACACGCAGGT | 93664 |
rs75706733 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | CADPS2 | GRCh38.p7 | 7:122828397 | TAAGCTTAGAACTTT[C/T]ATTTTTAAGATAATT | 93664 |
rs75708714 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122580401 | TGGGTTGCAATGAGC[C/T]GAGGTTGTGCCACTG | 93664 |
rs75711061 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122346210 | CATCTCTACAAAAAA[A/T]AAAAAAAAATAGCTG | 93664 |
rs75717637 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | CADPS2 | GRCh38.p7 | 7:122648276 | TCCTTGAGCTCTAGA[A/C]CCTCCCAAAGGGTTC | 93664 |
rs75727981 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122617214 | AAAACAATACTTCCA[A/G]CTGTGCTGGGAACGT | 93664 |
rs75733979 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122827184 | AGCTTACAGAAAAAT[A/G]TACCAATTCCTGAAG | 93664 |
rs75745311 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122590320 | CAGAAACCAACCCTC[A/C]CACATATGGTCAAAT | 93664 |
rs75745823 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | CADPS2 | GRCh38.p7 | 7:122394121 | TATTTGTGGATTTTC[C/T]TTTTAGTCATTCAAT | 93664 |
rs75763766 | snp | G/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122480682 | GTTTCTACTTTTTTT[G/T]TTGCGATAGACATTT | 93664 |
rs75765153 | snp | A/C | 0.00502683 | 0.0498813 | intron-variant | CADPS2 | GRCh38.p7 | 7:122663597 | CAAAACAAAACAAAA[A/C]AAAAAACAATTACAA | 93664 |
rs75774073 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122797418 | TTCACTGCAGCACTA[C/T]TCACAATAACAAACA | 93664 |
rs75778484 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122832317 | GTAAAAAAAAAAAAA[A/C]CCCACCCATGTGTGC | 93664 |
rs75781266 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122728436 | GATAGCTGGTGGTAG[A/G]AAATTGGAGTAGATA | 93664 |
rs75782521 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122663120 | CAAATTCAATTTTGC[A/T]CAACTTTCCAAGTAA | 93664 |
rs75792974 | snp | C/T | 0.000932749 | 0.0215755 | intron-variant | CADPS2 | GRCh38.p7 | 7:122407741 | AAGTAGATTACTTTT[C/T]AGAAACATGCACAAG | 93664 |
rs75809961 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | CADPS2 | GRCh38.p7 | 7:122482849 | AGACTCTCAAGATCT[A/G]CAGAAGGCCTCCCCC | 93664 |
rs75813679 | in-del | -/A | 0.395087 | 0.203592 | intron-variant | CADPS2 | GRCh38.p7 | 7:122474057 | TATAACAGAGGTTTT[-/A]AAAAAATCTTTATTT | 93664 |
rs75831117 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | CADPS2 | GRCh38.p7 | 7:122607575 | AAACTTTCTCCCAAA[C/T]TTTCTCATGCTGTTT | 93664 |
rs75850641 | snp | A/G | 0.147991 | 0.228242 | intron-variant | CADPS2 | GRCh38.p7 | 7:122375611 | CATCAACTAAACACC[A/G]TCAAGTAAAAATGGA | 93664 |
rs75855699 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122462656 | CAAGAATATAGAAAG[C/G]CTAACGATGTGAACA | 93664 |
rs75863711 | snp | C/G | 0.0479149 | 0.147179 | intron-variant | CADPS2 | GRCh38.p7 | 7:122876523 | TGAGTCGCCATGCTT[C/G]ACTAATTTTTTCTAT | 93664 |
rs75873931 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122799762 | ATATTAGTCAAAATA[C/T]ACCTAGCAATTAAAA | 93664 |
rs75879219 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122815623 | TAATGAAATACAAAA[A/T]AAATTCAAAATATAT | 93664 |
rs75880247 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122428718 | TCGTGATCCGCCAGC[C/T]TCGGCCTCCCAAAGT | 93664 |
rs75920560 | snp | A/C | 0.0314385 | 0.121371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122840673 | GTAGTCCCAGGTACT[A/C]CAGAGGCTGAGGCAG | 93664 |
rs75937039 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122867939 | TACCTGAAGGGGAAA[C/G]TGAGCACCCTCTGTG | 93664 |
rs75960578 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122431040 | AGCATTAGTGCTTCC[A/C]CCACTTCTTCCTGCC | 93664 |
rs75962897 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | CADPS2 | GRCh38.p7 | 7:122340158 | TAAGCCTTTATAAAA[C/T]GCTGTTTGGATGAAT | 93664 |
rs75971501 | snp | C/G | 0 | 0 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122562012 | AAGAGAAAAAGTCTT[C/G]ATAACTAAATTACTG | 93664 |
rs75976133 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122358553 | CATATATATTTTATC[C/T]TATATTTTCTTCTTG | 93664 |
rs75983695 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | CADPS2 | GRCh38.p7 | 7:122829365 | AGGATTAGAAATGCT[C/G]TCCCCTTCACACTTT | 93664 |
rs75984157 | snp | C/T | 1.77476e-05 | 0.00297884 | intron-variant | CADPS2 | GRCh38.p7 | 7:122345535 | TCTCTTTGCAGTTTA[C/T]CTATGGTGTCAGCAT | 93664 |
rs75989422 | snp | A/C | 0.0410537 | 0.137264 | utr-variant-3-prime | CADPS2 | GRCh38.p7 | 7:122318683 | CCGGAAGAAGGAAGA[A/C]ATTTCCTTGTTTGTT | 93664 |
rs75997753 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122786146 | CTAGAAGGGATAACA[A/C]GGACTTTTATTTTCT | 93664 |
rs76003428 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | CADPS2 | GRCh38.p7 | 7:122525589 | CCTGCCCTGCTCCCT[C/T]GTGTTTAAATACAGT | 93664 |
rs76021581 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122434160 | TTGCTAAAGAGCATC[A/G]GATTGTTGCTATTAC | 93664 |
rs76024358 | snp | C/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122816945 | AGGGAGCTTTCTGAG[C/T]CAGGATGAGCCAGGA | 93664 |
rs76028229 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122630391 | TCAAAAAAAAAAAAA[A/G]AGGAAGATGTTCCTA | 93664 |
rs76033349 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122719069 | AATCCCTCTACGTTA[C/T]ATAAACACAGCTCCC | 93664 |
rs76045933 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122352225 | TATTATATTCATAAG[A/T]AGCAATCATAATGAT | 93664 |
rs76046537 | in-del | -/ACT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122882635 | TTTTTTTTTTTTTTT[-/ACT]TTCTCCTCCGAGGTC | 93664 |
rs76060204 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122617553 | TAAAAAGAAGAGAGG[C/T]ATGTATAAAATGTGA | 93664 |
rs76062732 | snp | A/C | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122864535 | GCCACTTGTAGCTCT[A/C]AGGAAAGCTAGAAAA | 93664 |
rs76070193 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122527880 | CCCCCAAAACAGAGA[A/G]AGAAGGGTGAAAATA | 93664 |
rs76073848 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CADPS2 | GRCh38.p7 | 7:122852835 | GACTTCTGTTATAAC[A/G]GAATCCCTCTGACTA | 93664 |
rs76081752 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | CADPS2 | GRCh38.p7 | 7:122405270 | TAAAAACCTGACTGT[A/C]ATTTCATAGCAGAAA | 93664 |
rs76083091 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122655614 | GTGAAATAAAAAAAA[A/T]TTGTGTGACCTGCTT | 93664 |
rs76089400 | snp | A/G | 0.110167 | 0.207236 | intron-variant | CADPS2 | GRCh38.p7 | 7:122746350 | AATACCAGATTTCAA[A/G]CATTCAGAACCACAA | 93664 |
rs76089585 | snp | A/G | 0.433437 | 0.169856 | intron-variant | CADPS2 | GRCh38.p7 | 7:122822412 | ACTCTAGGTTCCCAC[A/G]CTGCCCCTAATCCTG | 93664 |
rs76093662 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | CADPS2 | GRCh38.p7 | 7:122407025 | TCAATAGAGAGCTTT[C/T]ACATTCTCCTTAATT | 93664 |
rs76098903 | snp | A/C | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122803999 | AAAAAAAAAAAAAAA[A/C]ACTGCAAAGCACACT | 93664 |
rs76100500 | snp | A/C | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122827633 | GCGAAATTCCATCTC[A/C]AAAAAAAAAAAGAAA | 93664 |
rs76106101 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122336866 | TGCATGTGGAATTTC[C/T]TTTTTTAATTCTGAG | 93664 |
rs76110238 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122773213 | ATGCTAGAAAGGACA[C/T]GGTGATATGGAAACG | 93664 |
rs76126779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122423141 | GAAAGTCTAAATTTT[C/T]ATCTAGATTTTCTGA | 93664 |
rs76136687 | snp | A/T | 0.0232847 | 0.105357 | intron-variant | CADPS2 | GRCh38.p7 | 7:122771121 | GGCAGGGCCTAGATA[A/T]CCTGGAATTTTCAAA | 93664 |
rs76137038 | snp | A/T | | | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122704537 | CTTTTTATTTTGCAG[A/T]TTTTTTGTGGGTGAA | 93664 |
rs76155289 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | CADPS2 | GRCh38.p7 | 7:122596778 | TTGAATCCTGGTTTC[C/T]CTACTGAAGAGCTGG | 93664 |
rs76158888 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | CADPS2 | GRCh38.p7 | 7:122831548 | TTCAATAATTCTTCC[A/T]GGAGGAGGGAAAGAA | 93664 |
rs76168058 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122414798 | TCTATGAATTGGCTT[A/T]AAATGTAGTTCCTGT | 93664 |
rs76168678 | snp | G/T | 0.0325976 | 0.123435 | intron-variant | CADPS2 | GRCh38.p7 | 7:122874143 | TAGTTTCTTTTGCTG[G/T]GCAGAAACTCTTTAG | 93664 |
rs76178932 | snp | C/G | 0.0566069 | 0.158427 | intron-variant | CADPS2 | GRCh38.p7 | 7:122417105 | TTTTTTCCTACAATA[C/G]TTTTCCCTTGATTTA | 93664 |
rs76181557 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122798323 | AAGGTAAAATGCCAC[G/T]CTCCCTAATGAATGT | 93664 |
rs76203417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122728815 | GCATAAGGTAACACT[A/G]ATGATAATTTTCTTA | 93664 |
rs76207177 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | CADPS2 | GRCh38.p7 | 7:122725348 | TCTTTTATATATATA[C/T]GTATAGGTATATATG | 93664 |
rs76208440 | snp | A/G | 0.0696718 | 0.173152 | intron-variant | CADPS2 | GRCh38.p7 | 7:122339222 | AAAAGTACATTATCA[A/G]CTCTAAATACATACA | 93664 |
rs76220744 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | CADPS2 | GRCh38.p7 | 7:122436867 | ATACAAAGATAAAGT[A/G]CACTGCATATATCTT | 93664 |
rs76228708 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | CADPS2 | GRCh38.p7 | 7:122332033 | GTCACTGCAACATAG[A/G]ATTATGCACAAATAG | 93664 |
rs76228973 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | CADPS2 | GRCh38.p7 | 7:122865992 | CATCTTATTTTGATG[C/T]TGGAAGTATTTTCCC | 93664 |
rs76233656 | in-del | -/T | 0.172997 | 0.237846 | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122704537 | TTTTTATTTTGCAGA[-/T]TTTTTTGTGGGTGAA | 93664 |
rs76245249 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122494373 | AGTATTGCATATAAG[C/T]GGTTTGGTTAAAATA | 93664 |
rs76250134 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122512096 | TACTTTTTAGCCAGG[A/G]AAAAAAAAATAGGCT | 93664 |
rs76252061 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | CADPS2 | GRCh38.p7 | 7:122714306 | AAGTAGCAGTCTATA[C/T]CTACAAGAATACAAA | 93664 |
rs76252946 | snp | A/C | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122580455 | AAGATTCTGTCTCAA[A/C]AAAAAAAAAAAACCC | 93664 |
rs76274258 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122646779 | GGAAGGTGCTTCAAT[G/T]ATGTTTATCTAAAAA | 93664 |
rs76304357 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122728415 | GAAATGGAATGATAC[A/C]AATCTGATAGCTGGT | 93664 |
rs76307092 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | CADPS2 | GRCh38.p7 | 7:122444989 | CCGACAGATGCTACC[C/T]GAACTATTGGATATT | 93664 |
rs76307528 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122868582 | ATCCCTGATTGGAAA[G/T]AAAGATCTTTTACGC | 93664 |
rs76309844 | snp | C/T | 0.18989 | 0.242666 | intron-variant | CADPS2 | GRCh38.p7 | 7:122611092 | GGAAATTTATAGCTG[C/T]AATTGCCTATTTTAA | 93664 |
rs76325245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122486755 | TACCAGAAAATCTTT[C/T]GTGAAAGAATCAGTC | 93664 |
rs76333995 | snp | A/C | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122418172 | GAGACTCCATCTCAA[A/C]AAAAAAAAAAAAAGT | 93664 |
rs76343501 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122537290 | AATACAAGCAAAAAA[A/C]AAACAAACAAACAAA | 93664 |
rs76350497 | snp | G/T | 0.126564 | 0.217402 | intron-variant | CADPS2 | GRCh38.p7 | 7:122440525 | CAGGGATAAGACAGG[G/T]ATATAAAAATAAAAT | 93664 |
rs76361970 | snp | C/T | 0.021333 | 0.101051 | intron-variant | CADPS2 | GRCh38.p7 | 7:122351729 | AAAGGCAGAATCCTA[C/T]CTTAATGCTATGAAG | 93664 |
rs76366328 | snp | A/G | 0.204496 | 0.245824 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122544505 | ACCTGAGCTGGGCAG[A/G]CCATGACCAACTCGT | 93664 |
rs76400058 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122716849 | ATGGAGGGAGGCCCA[A/G]AAAGGGAAACACTGA | 93664 |
rs76408887 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122369141 | TTCCCCCCCCCCCCC[C/T]CTTTTTTTTTTTTTG | 93664 |
rs76409460 | snp | A/G | 0.0785177 | 0.181917 | intron-variant | CADPS2 | GRCh38.p7 | 7:122682207 | TCCAATCTGTTTGAC[A/G]CTGTGCAACAAAGAC | 93664 |
rs76409643 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122754409 | AAATTTAATTAAAAT[G/T]ACTTACTAAAAGGCC | 93664 |
rs76415867 | snp | G/T | 0.0263992 | 0.111815 | intron-variant | CADPS2 | GRCh38.p7 | 7:122503875 | AATTGCAATTAGGAG[G/T]TACTGAAAATAATTT | 93664 |
rs76424547 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | CADPS2 | GRCh38.p7 | 7:122861754 | GATCATTACGCACTA[C/T]GCGTATATATTGAAA | 93664 |
rs76429478 | snp | A/C | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122425428 | CCCTATCTCTACCAA[A/C]AAAAAAAAAAAAAAA | 93664 |
rs76432533 | snp | A/C | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122511940 | GTTTTTGAAAAATAG[A/C]TGACCCACAACCCCA | 93664 |
rs76466810 | snp | C/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122882860 | TCACTACTGACATCA[C/G]TTTCAATCACTGTTT | 93664 |
rs76470884 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | CADPS2 | GRCh38.p7 | 7:122384071 | CTGAGGTGGCTTTGT[A/G]ATCTCGACATCTGTC | 93664 |
rs76476248 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122752132 | GTGAATAAATAGAAT[A/G]GAAAAACTTAAATAT | 93664 |
rs76495023 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122678073 | AGTATCATTAGACAC[G/T]CAAATTTTAAAGGAA | 93664 |
rs76528953 | snp | C/T | 0.00507704 | 0.0501273 | missense | CADPS2 | GRCh38.p7 | 7:122387076 | TTTGCTTTTTGGCAT[C/T]GACTAATACATTAAA | 93664 |
rs76534963 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122602384 | TATAACGTGTATATA[C/T]AGAAACACACCATGG | 93664 |
rs76536467 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122399026 | TGTATACATTAACTA[G/T]TATAATAACCCCTAA | 93664 |
rs76543630 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122822488 | CCCCCCAAAAATTTT[C/T]GCCGCCCCAACACTT | 93664 |
rs76550290 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | CADPS2 | GRCh38.p7 | 7:122595591 | TATCAGAGCAGTAAC[A/G]TGGAGGACTTTACAG | 93664 |
rs76565711 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122668725 | ATAAGAGAAATCAGG[A/T]CAAATGAAGAGAGAT | 93664 |
rs76573357 | snp | A/T | 0.021333 | 0.101051 | utr-variant-3-prime | CADPS2 | GRCh38.p7 | 7:122320034 | CTCTACATTCAGGCT[A/T]ACTTTTTAAAGAAAT | 93664 |
rs76606733 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122731360 | CCTTTTGGAAATCTA[C/G]AAGAGAAAGACCATT | 93664 |
rs76610372 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122578220 | GTGTGCACATATATA[C/T]ATACCCACACACACA | 93664 |
rs76617545 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122523532 | ATATTTATACGACTG[C/T]ATAAATATGTTAGGT | 93664 |
rs76626234 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122616891 | TATAACCATATTAAT[A/T]AAAAGGCAACTACAC | 93664 |
rs76633099 | snp | C/T | 0.030665 | 0.119967 | intron-variant | CADPS2 | GRCh38.p7 | 7:122765557 | CCTACTTCATGAACA[C/T]TGTTACAATGTCTAT | 93664 |
rs76636080 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | CADPS2 | GRCh38.p7 | 7:122425224 | GAGCTCAAGTGATCC[A/G]TCTTTATCAGGCTCC | 93664 |
rs76640208 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | CADPS2 | GRCh38.p7 | 7:122864507 | AACAAACCAAAAAAA[C/T]TTATGTCACATGGCC | 93664 |
rs76640820 | in-del | -/GA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122711881 | GGTCTCGAACTCCTG[-/GA]ACCTTGTGATCCACC | 93664 |
rs76641671 | snp | G/T | 0.030278 | 0.119257 | intron-variant | CADPS2 | GRCh38.p7 | 7:122849125 | TACACGGACAACTCA[G/T]AAATTTGCATTTATA | 93664 |
rs76645475 | snp | A/G | 0.15665 | 0.231917 | intron-variant | CADPS2 | GRCh38.p7 | 7:122522776 | ATCATTCTAACTTCT[A/G]TCTCCACAGATCAAC | 93664 |
rs76656268 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122370592 | GGATTCAGAGACACA[C/T]ACATAACCATGAAGA | 93664 |
rs76669089 | snp | A/G | 0.172997 | 0.237846 | intron-variant, upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122622068 | CACTAGTAGCTTTGC[A/G]ATGCTTGGGATAACT | 93664 |
rs76674935 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | CADPS2 | GRCh38.p7 | 7:122607010 | ACCTGATATGACAAA[C/T]GGCATTTGCTAACCA | 93664 |
rs76677037 | in-del | -/TTACT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122729696 | TTTTTTTTTTTTTTT[-/TTACT]GTTGAGTCCTTTGAG | 93664 |
rs76691011 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | CADPS2 | GRCh38.p7 | 7:122344566 | CTGCATATTTTAGCA[C/T]ATATCAGTACTTTAA | 93664 |
rs76696353 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | CADPS2 | GRCh38.p7 | 7:122711339 | ATGTAAATGAATATA[C/T]AGCTATATCTCTCAA | 93664 |
rs76707163 | snp | A/T | 0.0283406 | 0.115616 | intron-variant | CADPS2 | GRCh38.p7 | 7:122368875 | AGGCTGTCAGTTTTT[A/T]AAAAACCCAATACCC | 93664 |
rs76707642 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | CADPS2 | GRCh38.p7 | 7:122705262 | CATGTGACTGGGAGA[C/G]AGAGAGAGAGACTGG | 93664 |
rs76716660 | snp | A/G | 0.000903705 | 0.0212376 | missense | CADPS2 | GRCh38.p7 | 7:122325496 | ACAATCTTGATGAGC[A/G]TCTTCAGCTGGTAAA | 93664 |
rs76719194 | snp | C/T | 0.377187 | 0.215229 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122532633 | CTCAGGTGATGCTGA[C/T]GCTGCTGGCCTGGTA | 93664 |
rs76732945 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122343043 | CTACTTTGCCTTTCA[A/G]CACGTACTTGATAAC | 93664 |
rs76735099 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122520331 | TTACATAGTACCCGG[G/T]TGAATGTGTGTGTTT | 93664 |
rs76738669 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122515830 | TAATAAAAAAATTAA[A/T]TAAAAAATAATAATA | 93664 |
rs76755844 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122557755 | TGAACTATGGCACAC[C/T]GGCTGGCTATTTGCC | 93664 |
rs76761231 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122441139 | TTGGCATGAGGACTA[C/T]GACAGGTAGAAGTAC | 93664 |
rs76775158 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | CADPS2 | GRCh38.p7 | 7:122692376 | GGTTCTTTCTCCCTG[C/T]GCTGCATCCTGCAGG | 93664 |
rs76785466 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | CADPS2 | GRCh38.p7 | 7:122402106 | AATTAGTTCAGTCTC[C/T]AGAAGTCTTGTCACA | 93664 |
rs76789152 | snp | C/T | 0.291235 | 0.246576 | intron-variant | CADPS2 | GRCh38.p7 | 7:122634386 | TTTTCACTTCCTGCC[C/T]GGTTCAATCTTGGGA | 93664 |
rs76814467 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | CADPS2 | GRCh38.p7 | 7:122584429 | ATCCTTATAGCATCT[A/G]TTATGTCCTTCTTCA | 93664 |
rs76818609 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554422 | AGTAAGATAACTTAC[A/G]TATGTCACTTTTTGA | 93664 |
rs76821426 | snp | A/C | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122385573 | ATTCTAACTCACGAC[A/C]AAAAAAAAAGTATAC | 93664 |
rs76824312 | snp | C/T | 0.039522 | 0.134904 | intron-variant | CADPS2 | GRCh38.p7 | 7:122424322 | AGTCACATTAACTAC[C/T]TTACCTAGATTATCT | 93664 |
rs76827904 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122786328 | AGGAGGCAGAATTAA[A/G]CACAGTCAAGACACT | 93664 |
rs76828777 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | CADPS2 | GRCh38.p7 | 7:122491896 | GACTTTTAACAAAGT[A/G]AAAAAAGATCTCACG | 93664 |
rs76832266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122415831 | ATACACACACACAAT[C/T]GCTTTGTAATATATA | 93664 |
rs76874712 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122610444 | AAGCAAAAAAAAAAA[A/T]CCAGATACAAAGACT | 93664 |
rs76886054 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | CADPS2 | GRCh38.p7 | 7:122849116 | ACTAAACTATACACG[G/T]ACAACTCAGAAATTT | 93664 |
rs76893555 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122629153 | AAAATTATGCTGGCT[C/T]TTTTTTTTTTAACCT | 93664 |
rs76904831 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | CADPS2 | GRCh38.p7 | 7:122761198 | AGCCTGGGAAACCCA[C/G]ACATAACTGAAAGTG | 93664 |
rs76919178 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | CADPS2, LOC105375481 | GRCh38.p7 | 7:122528985 | AATTCTACTTAAATA[A/C]GTGCCACTTTTATTA | 93664 |
rs76923714 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122351039 | TGCATTTTAAAAATA[A/G]ATTTTTAAAAACCAT | 93664 |
rs76926603 | snp | C/G | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122673395 | CCTGAGCTAGACACA[C/G]ATTGCTGATTGGTGT | 93664 |
rs76938095 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | CADPS2 | GRCh38.p7 | 7:122415893 | TCTCATGTGTGAATG[C/T]GCAATGGGATGTACA | 93664 |
rs76940452 | snp | A/G | 0.0667028 | 0.170006 | intron-variant | CADPS2 | GRCh38.p7 | 7:122604001 | TAGTAACTTGATTGT[A/G]ATAATCATTATACAA | 93664 |
rs76943240 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122488486 | TGATGTAAGGAATTC[A/G]TAGGTGTCTGGAGTT | 93664 |
rs76948438 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122515785 | AACTAACCTGCACAA[C/T]GTGCACATGTACCCT | 93664 |
rs76958329 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | CADPS2 | GRCh38.p7 | 7:122499741 | TGTGTGAAATGTGTC[C/T]TATGTATCCTTAAGT | 93664 |
rs76962686 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | CADPS2 | GRCh38.p7 | 7:122451092 | AGTCACCAGAGCTAG[A/G]GGGAAGAGACTATGC | 93664 |
rs76965261 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122515068 | AGTTACTAAAAGTCA[A/G]AATAAAAACAAAGTT | 93664 |
rs76975744 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122389649 | TGAAAGTAAAATATT[C/T]CTACATTAAAACATA | 93664 |
rs76983254 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | CADPS2 | GRCh38.p7 | 7:122488471 | AGAATCTGATGAAAA[C/T]GATGTAAGGAATTCA | 93664 |
rs76983342 | snp | C/T | 0.0640965 | 0.167152 | intron-variant | CADPS2 | GRCh38.p7 | 7:122513996 | TCAACTTTGCATTGA[C/T]CTTAGTAAGCTGAAT | 93664 |
rs76990484 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122691135 | GCACCGTCCTTATCC[A/G]GGGAGTCACTACCCA | 93664 |
rs77042132 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | CADPS2 | GRCh38.p7 | 7:122740856 | AAAATGGACAAAATT[G/T]ATATGTTCAGATAAA | 93664 |
rs77045439 | snp | C/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122748828 | TTAGAATGCTTTTCA[C/G]TGAAAGTAATAGAAT | 93664 |
rs77046201 | snp | C/T | 0.030278 | 0.119257 | intron-variant | CADPS2 | GRCh38.p7 | 7:122771846 | AAGCTGGAAATAACA[C/T]AGAAAAAGAGTGTCA | 93664 |
rs77073850 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122628669 | GTACTAGAAAAAACT[C/G]ATGCCTTTTGTCTGA | 93664 |
rs77080552 | snp | G/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122346412 | AACCAAAAAATGTTA[G/T]CTTTCCTTAGGGTGC | 93664 |
rs77082944 | snp | A/C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122686408 | CTATTATACTATTTT[A/C/T]ATTACAGCTGTGATG | 93664 |
rs77096033 | snp | C/T | 0.0327778 | 0.123752 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122551530 | TGTTACAATAGTTCA[C/T]GCAAGAAAGATCTAT | 93664 |
rs77106934 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122788209 | CCTTTCTTTGTCTAC[C/T]AGTAGTTTTCTGACT | 93664 |
rs77110559 | snp | C/T | 0.0770498 | 0.180522 | intron-variant | CADPS2 | GRCh38.p7 | 7:122670862 | GCACAGCAGTGAAAC[C/T]CTGTTTCAAAAAAAA | 93664 |
rs77165101 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122804511 | TCATTTAATTTATTG[G/T]TTTTAATAGAAAATT | 93664 |
rs77172271 | snp | C/G | 0.0368353 | 0.130617 | intron-variant | CADPS2 | GRCh38.p7 | 7:122347078 | AAATAAGCCAGTTAG[C/G]CTTGCATCATTTCGT | 93664 |
rs77177873 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122887808 | TACTGACATTCTCTC[C/T]AGATGGGTAAAAGAC | 93664 |
rs77188325 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122380963 | AGACAGAAAAACAGG[A/T]AGAAGAAAAAGAGCC | 93664 |
rs77192491 | snp | G/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122625066 | TTATTTTTTTTTTTT[G/T]TGAGACAGAGTTTCG | 93664 |
rs77208745 | snp | A/G | 0.030278 | 0.119257 | intron-variant | CADPS2 | GRCh38.p7 | 7:122752892 | CACATAAAAGAGAAA[A/G]GAAAGACAAACAAGA | 93664 |
rs77228644 | snp | A/G | 0.030665 | 0.119967 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122548859 | TCCCTTGGACATAGA[A/G]AGAAGACAAAATAAA | 93664 |
rs77246901 | snp | A/G | 0.219648 | 0.248151 | intron-variant | CADPS2 | GRCh38.p7 | 7:122644884 | AAGAACTCTCTTATA[A/G]CTACCTTCTAAATTA | 93664 |
rs77253076 | snp | C/T | 0.0637235 | 0.166737 | intron-variant | CADPS2 | GRCh38.p7 | 7:122486898 | CTACCAGCAAAAATA[C/T]TATAATCACTGAAGT | 93664 |
rs77256000 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122600497 | CATCAAAAAAGTGAC[G/T]AATCACATTAAGTCC | 93664 |
rs77281169 | snp | A/C | 0.5 | 0 | utr-variant-3-prime | CADPS2 | GRCh38.p7 | 7:122319947 | AGGATGCTCTTCTCC[A/C]AAAAAACAAACAAAC | 93664 |
rs77299929 | snp | C/T | 0.00239473 | 0.03452 | intron-variant | CADPS2 | GRCh38.p7 | 7:122380927 | TGAAGAGAAGGAAAA[C/T]GGGAGAGAAAAGGGG | 93664 |
rs77307810 | snp | A/G | 0.030278 | 0.119257 | intron-variant | CADPS2 | GRCh38.p7 | 7:122725052 | GAGTAATGTAGTTTC[A/G]GTGTAGTTCATGAAC | 93664 |
rs77318989 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122617148 | TACTATAAGCTACTG[G/T]AAACATGACCTCCTA | 93664 |
rs77327717 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122462657 | AAGAATATAGAAAGG[C/T]TAACGATGTGAACAT | 93664 |
rs77333269 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | CADPS2 | GRCh38.p7 | 7:122469740 | TGTAACACACTGTTT[C/T]AGGTACGTGGAGGAT | 93664 |
rs77339747 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | CADPS2 | GRCh38.p7 | 7:122519019 | ATGGAAAAACAAAAG[A/G]ACACAAATATCATCA | 93664 |
rs77342258 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | CADPS2 | GRCh38.p7 | 7:122496567 | GCCTCATCTCACAAG[G/T]AGCATTTTTATGAGT | 93664 |
rs77348496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122818703 | TGGTCCGGCTTACAG[C/T]TTCGTTCCCTGACTA | 93664 |
rs77355890 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | CADPS2 | GRCh38.p7 | 7:122636886 | TTCTTAAATTTGTAC[A/G]TCCAACTCTCTAGTG | 93664 |
rs77360429 | snp | C/T | 0.0984431 | 0.198823 | intron-variant | CADPS2 | GRCh38.p7 | 7:122476487 | TCTATAATTAAATCA[C/T]ATTTTTGTAAATTTA | 93664 |
rs77360816 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | CADPS2 | GRCh38.p7 | 7:122813823 | TTTTAAACCATATAT[G/T]TACTAACTTCCCATT | 93664 |
rs77391624 | in-del | -/GATGGTAAT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122814212 | TCAAGCAGAGGTTTT[-/GATGGTAAT]AACGTGACTAGTAAA | 93664 |
rs77424772 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | CADPS2 | GRCh38.p7 | 7:122522750 | AACACCCTTCCCAGC[C/T]TCTGGTAATTATCAT | 93664 |
rs77454053 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122669898 | GCTTGCCTATCTCAG[C/T]GAGTGACAGATCCCA | 93664 |
rs77455668 | snp | A/C | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122477540 | CGCCACCCCCGACCC[A/C]ACCAAAAAAAAAAAA | 93664 |
rs77462788 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | CADPS2 | GRCh38.p7 | 7:122402924 | GACAATAACTCTAAT[C/T]GGGTCAACATGGTAA | 93664 |
rs77466975 | snp | A/G | 0.257732 | 0.24988 | intron-variant | CADPS2 | GRCh38.p7 | 7:122679472 | TGTGCACAGCAGGAC[A/G]TGGACGTTCATTAGT | 93664 |
rs77468043 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122755447 | AGCTATATATTATCA[A/G]CACTGTATTGTATTT | 93664 |
rs77474569 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | CADPS2 | GRCh38.p7 | 7:122483771 | CTATACATGAAGATA[C/T]ATAATAAATTTAAAG | 93664 |
rs77475926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122658644 | GAACATGCAGTGTTT[A/G]GTTTTCTGCTCCTGT | 93664 |
rs77499420 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122504767 | ATGGGGTCTCACTAC[A/G]TTGTTCAGACTGGTC | 93664 |
rs77500267 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122708698 | ATAAACTAAATTAAA[C/T]TCTCTTCTTCATTCA | 93664 |
rs77500938 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122874146 | TTTCTTTTGCTGTGC[-/A]GAAGCTCTTTAGTTT | 93664 |
rs77505015 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122714471 | TTTTAATGTTTTACT[A/G]TCATCATTTTTTTAA | 93664 |
rs77509582 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122761690 | AGCAAACAAAAAAAA[A/G]GCTCTTGAAAATTAA | 93664 |
rs77512676 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122418637 | ATGATAGTAGGAATA[A/G]AAAAGAAGGGAAAGA | 93664 |
rs77521322 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122750696 | TAAAGAAAGAAGAAC[A/G]AGTGAACAAATCCCA | 93664 |
rs77531465 | snp | C/G | 0.0333695 | 0.124785 | intron-variant | CADPS2 | GRCh38.p7 | 7:122827133 | CAGTAAAATATGAGA[C/G]ACTACTATGAACAAC | 93664 |
rs77551216 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122385597 | AGTATACACTAGTCA[A/G]TCCTTTACGCATAAA | 93664 |
rs77554783 | snp | C/T | 0.0718919 | 0.175435 | intron-variant | CADPS2 | GRCh38.p7 | 7:122640222 | CCACATAGTTGAGAC[C/T]TAGGCAGACCAGTAT | 93664 |
rs77559868 | snp | C/G | 0.0581099 | 0.160244 | upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122887862 | GTCTTACCTATTTTT[C/G]TGCCTAATCCATAAC | 93664 |
rs77574085 | snp | A/T | 0.20111 | 0.245173 | intron-variant | CADPS2 | GRCh38.p7 | 7:122363548 | TGTTGATGAATTTAC[A/T]TCTTGGCTCAAGTTG | 93664 |
rs77575106 | snp | C/G | 0.194902 | 0.243853 | intron-variant | CADPS2 | GRCh38.p7 | 7:122357784 | TATGCATTTAAGATT[C/G]ATCCATGTCTTCATG | 93664 |
rs77605410 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122594760 | TTTTAAAGAGAACAA[A/G]TTGGTCACATCTTGG | 93664 |
rs77627777 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | CADPS2 | GRCh38.p7 | 7:122392584 | TGCAATAGGCAAGCT[C/T]ATCATGATGTGAAGT | 93664 |
rs77633002 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | CADPS2 | GRCh38.p7 | 7:122480550 | AGTGAAAATAATACC[A/G]CATGTATAACTTAGC | 93664 |
rs77687318 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122704364 | AGACTTTTTTTTTTT[C/T]ATGTTCAAATGGAGT | 93664 |
rs77697497 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122580373 | GGCACAAGAATCGCT[C/T]GAATCTAGGAGGTGG | 93664 |
rs77706461 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | CADPS2 | GRCh38.p7 | 7:122720525 | GTATATATACATATG[C/T]GTATGCAGATATGTA | 93664 |
rs77707771 | snp | A/C | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122415604 | CAAATACAGAACCAA[A/C]AAAAAAAAAAAAAAA | 93664 |
rs77711660 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122749227 | CTAAAGAAATCAATG[C/G]GTAAGGGAAATGGAA | 93664 |
rs77715333 | snp | G/T | 0.0287284 | 0.116357 | intron-variant | CADPS2 | GRCh38.p7 | 7:122618558 | AAATTTGAGGAGAGT[G/T]TTTCAAATCTGCACT | 93664 |
rs77737616 | snp | C/T | 0.030278 | 0.119257 | intron-variant | CADPS2 | GRCh38.p7 | 7:122745298 | AACATGTCTGATTAA[C/T]CTTCTTAAAATTCTC | 93664 |
rs77756155 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | CADPS2 | GRCh38.p7 | 7:122518969 | AATATTTTGTTGTCA[C/T]CTTTGTCAAATTCTT | 93664 |
rs77766142 | snp | A/G | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122658928 | ATATGTAAAAAAAAA[A/G]GTTTCTCGTACTTAT | 93664 |
rs77784198 | snp | A/G | 0.204496 | 0.245824 | intron-variant | CADPS2 | GRCh38.p7 | 7:122571718 | TTCGTCACTGGTGTG[A/G]TGACTGAGATATGAT | 93664 |
rs77790568 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | CADPS2 | GRCh38.p7 | 7:122758864 | ATCACCAGAGTTTAG[C/G]GGAGGAAAAAAACAG | 93664 |
rs77800733 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | CADPS2 | GRCh38.p7 | 7:122401043 | TTGCCAGTCACTCTG[A/G]GCTCTATTATGGCTA | 93664 |
rs77803096 | in-del | -/AA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122796752 | AACTCCAAACTCTGG[-/AA]AAAAAAAAAACCGTA | 93664 |
rs77805750 | snp | A/C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122853212 | ATGAGATACTAGCAG[A/C/G]AGATCAGATAAACGA | 93664 |
rs77819717 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122757091 | GGAAGCTCTGAACTG[G/T]TGACCAAAGGGCAAT | 93664 |
rs77828464 | snp | C/G | 0.0614824 | 0.164198 | intron-variant | CADPS2 | GRCh38.p7 | 7:122423444 | AACTTTGTAAGAAGA[C/G]TGCCTCAAAATCTGG | 93664 |
rs77841262 | snp | A/G | 0.0345262 | 0.126772 | intron-variant, nc-transcript-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122530303 | AAAGGTTTCCACTTA[A/G]GCTTAAGTTAGCTTT | 93664 |
rs77852222 | snp | C/T | 0.0722614 | 0.17581 | intron-variant | CADPS2 | GRCh38.p7 | 7:122623836 | GGCGAGCATGTCACG[C/T]ATCTGAAAGTTCTGA | 93664 |
rs77855947 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122823877 | GCATCAGACTCAGGG[C/G]TTGTGCAGGAGGGTG | 93664 |
rs77858997 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122531660 | ATTGCTTCAAAGAAT[C/T]ATCCAGAGGATCAAA | 93664 |
rs77860688 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122443987 | CTGCAAGTCTTCCCC[C/T]CAGATCACAGGCAAC | 93664 |
rs77862225 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122619476 | AAAAAAAAAAAAAAA[A/T]TTTAGCCAGGCATTG | 93664 |
rs77864415 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122739853 | CTGTATACCAAGAGA[C/T]AGACCAGTGGAACAG | 93664 |
rs77871897 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | CADPS2 | GRCh38.p7 | 7:122447626 | TCAGGCGATCTCGGC[C/T]CACTGCAGCCTCTGC | 93664 |
rs77899097 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122841823 | AAAGTTTAGTACTGT[-/C]AYTTTTTTTACCCTA | 93664 |
rs77911738 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122658743 | CCTTTGTGGTGTGGA[C/T]GAGTGGGGAGGGGAT | 93664 |
rs77915212 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122560265 | ATACAAGAAGGTAGG[C/T]TGAAGGAGATACCAG | 93664 |
rs77916743 | snp | A/T | 0.0633504 | 0.166319 | intron-variant | CADPS2 | GRCh38.p7 | 7:122340409 | GTGGGCAGTGCCCAA[A/T]AAATGCACAATGGTT | 93664 |
rs77917683 | snp | A/C | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122790396 | AGCCAGACAGCGTTT[A/C]TAAAAAAAAAAAAAA | 93664 |
rs77924588 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | CADPS2 | GRCh38.p7 | 7:122384945 | AACATTTACTAAAGT[A/G]CCTACTGCATGTCAG | 93664 |
rs77929503 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant, utr-variant-5-prime | CADPS2, RNF148 | GRCh38.p7 | 7:122702807 | ACAACATCAGTTGTA[C/G]AAGAACATAAAGAAG | 93664 |
rs77931572 | snp | G/T | 0.0165278 | 0.0893908 | intron-variant | CADPS2 | GRCh38.p7 | 7:122331070 | AAACCCAGTTGTCAT[G/T]CTGTTTTTATATGTT | 93664 |
rs77937994 | snp | A/G/T | 0.0528381 | 0.153711 | intron-variant | CADPS2 | GRCh38.p7 | 7:122331827 | GACTTAAGTGGTAGG[A/G/T]TAAAGATTTATATCT | 93664 |
rs77938085 | snp | G/T | 0.040671 | 0.13668 | intron-variant | CADPS2 | GRCh38.p7 | 7:122500130 | GAAAAATATCACCTT[G/T]ATGTTTAAAATTCCA | 93664 |
rs77939102 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122837564 | AAAAGAGAGAAGAAT[C/T]AAATAGACGCAATAA | 93664 |
rs77939692 | snp | G/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122729677 | GCCCATTTTTAACGG[G/T]TTTTTTTTTTTTTTT | 93664 |
rs77941650 | snp | A/C | 0.021333 | 0.101051 | intron-variant | CADPS2 | GRCh38.p7 | 7:122667500 | TGTAATGTAATCAAC[A/C]TTTAGTGTCAACAAC | 93664 |
rs77951301 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | CADPS2 | GRCh38.p7 | 7:122718191 | TAGAAGCTTTATATA[G/T]GTAGTTTATGTGATT | 93664 |
rs77952985 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122782704 | AATTATAGCACATCA[A/C]CAGATACTAAGAAAG | 93664 |
rs77977266 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | CADPS2 | GRCh38.p7 | 7:122487669 | GAGCTCTATGGAAAA[C/T]TATTAAAATGTAAAG | 93664 |
rs77992379 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122718050 | GCCCAGACTGGTCTC[A/G]AACTCCTGGACTCAA | 93664 |
rs78003272 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122625465 | AACATTTACAATCAG[A/T]AAATTCAGTAAATCG | 93664 |
rs78019611 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122507011 | CAGATAAAGTAGACT[A/C]AAAGAAAGATAAGAT | 93664 |
rs78019976 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | CADPS2 | GRCh38.p7 | 7:122483412 | TAAATACTTTTTTTC[A/G]TATATAAAGAAGCTA | 93664 |
rs78023372 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122684022 | CCTTAACTAAAATAA[A/G]TGGATAATTGTCTTA | 93664 |
rs78037971 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122814978 | AATTATTCCTAGGTC[A/G]GCCCCAGAACTCTTG | 93664 |
rs78040067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122621864 | CACTAGGCTGTAAAA[C/T]CCTCAGGCTTTGGCA | 93664 |
rs78052063 | snp | G/T | 0.0349115 | 0.127424 | intron-variant | CADPS2 | GRCh38.p7 | 7:122754797 | TTCAAACTTTTAATC[G/T]TATGAATGTAATAAC | 93664 |
rs78062341 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122700980 | TTGGAAACTAGATTT[C/G]CTGGGTATTAATAAA | 93664 |
rs78066721 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | CADPS2 | GRCh38.p7 | 7:122802261 | TAAAAACTGACATGC[A/G]TTTACAATTCATTTT | 93664 |
rs78076710 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122516427 | CTTGTCTTTGCTACT[A/T]GGGAGGAGGCTGAGG | 93664 |
rs78080820 | snp | C/T | 0.0763149 | 0.179815 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122533941 | TGTATGAGAGAACGT[C/T]CAAGATTTCCATTTA | 93664 |
rs78084458 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | CADPS2 | GRCh38.p7 | 7:122742553 | CTCTTAGGATAGTGT[A/G]GCCAACAGAGAGATA | 93664 |
rs78086317 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | CADPS2 | GRCh38.p7 | 7:122715374 | GTAAGGTTTCTCCTT[C/T]CAGAACGCAGATGGC | 93664 |
rs78089888 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122750613 | AATTTCCACAGCAGA[A/G]CTTGACATCCTGTGC | 93664 |
rs78099125 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122629154 | AAATTATGCTGGCTC[C/T]TTTTTTTTTAACCTA | 93664 |
rs78106015 | snp | G/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122625067 | TATTTTTTTTTTTTT[G/T]GAGACAGAGTTTCGC | 93664 |
rs78106222 | snp | A/G | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122630390 | GTCAAAAAAAAAAAA[A/G]GAGGAAGATGTTCCT | 93664 |
rs78111510 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | CADPS2 | GRCh38.p7 | 7:122747390 | AAAATTTCTACCCAA[C/T]GCTTTTCTACAAATA | 93664 |
rs78114414 | snp | A/C | 0.0298908 | 0.118541 | intron-variant | CADPS2 | GRCh38.p7 | 7:122732384 | ACTATATAGACCTAC[A/C]ATCAAGATGGAAAAG | 93664 |
rs78133124 | snp | C/T | 0.000243605 | 0.0110337 | intron-variant | CADPS2 | GRCh38.p7 | 7:122436328 | CCACCACATGAGAAA[C/T]AATGGCTTGTGCATG | 93664 |
rs78133583 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122348658 | CCTATTCTTGAAATT[A/G]TGACATATGGGAATT | 93664 |
rs78136903 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122538569 | AAAACTCCACCAATA[C/T]AAATTACTATATTGA | 93664 |
rs78142049 | snp | C/T | 0.205417 | 0.245993 | intron-variant | CADPS2 | GRCh38.p7 | 7:122575086 | TGAAAAAAATAGTCT[C/T]ATTTTTTTCTTATTC | 93664 |
rs78143432 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122864487 | TCTGTCTCAAAAAAC[A/G]AAAAAACAAACCAAA | 93664 |
rs78146045 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122668826 | TCTCATCTCCTGAGA[C/G]GAAGCCCTGTCTTCC | 93664 |
rs78146910 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | CADPS2 | GRCh38.p7 | 7:122651992 | TACTCCAGTAGTCAA[C/T]GATGTGAAGTTCCCC | 93664 |
rs78171938 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | CADPS2 | GRCh38.p7 | 7:122614052 | AGCAGCTATACAAAG[A/G]TAAGAGGGAAGATGA | 93664 |
rs78172434 | in-del | -/CTTT | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539835 | TCTCTCTCTTTCTTT[-/CTTT]AGTAAAGCATGCTTT | 93664 |
rs78173475 | snp | C/T | 0.021333 | 0.101051 | intron-variant | CADPS2 | GRCh38.p7 | 7:122424725 | GCCCAATTTGAGTTT[C/T]ATTAAAGTTGTCTTT | 93664 |
rs78187320 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122700832 | TTTAAAGAGCTCTGG[C/T]AAACAAAAGTGAATG | 93664 |
rs78201090 | snp | G/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122718009 | TTTTTTTTTTTTTTT[G/T]TGTAGAGACAAAGTC | 93664 |
rs78207738 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122762699 | TTAACCAAGGAGAGA[A/G]GAAAAGGGAATTTTC | 93664 |
rs78220034 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122847911 | TGGTTGAAAGCAATA[C/T]GGTAGCAAAGCCAGT | 93664 |
rs78222799 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122844916 | AGGTAAAAAAAAAAA[-/A]ATCATTTTATTCTAA | 93664 |
rs78228826 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122533542 | CACACCTTTTGGTGG[C/T]ACCAATATAATGGGG | 93664 |
rs78232637 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122358124 | TGCTCTCTTATCCTC[C/G]TCAACATTTTGCTGT | 93664 |
rs78235665 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122522979 | CATTCATTTGTTGAT[A/C]AACAGGCTGATTTCA | 93664 |
rs78260887 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122398778 | TCCCGCCGCCCTCCC[C/T]ACCCCTCACCCCTTC | 93664 |
rs78273783 | snp | C/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122493722 | GGTTATGTTTAATCT[C/T]TTTTTTTTTTTTTTT | 93664 |
rs78291189 | snp | A/T | 0.158962 | 0.232835 | intron-variant | CADPS2 | GRCh38.p7 | 7:122668942 | TTGTCCATTCCTCCA[A/T]CAAAACAGAAGGTAA | 93664 |
rs78302627 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122878772 | TACAACCTGTAATTA[C/T]TGAACATTAGCCCAC | 93664 |
rs78304097 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122747840 | TGTCATTGTGCCTTT[A/G]CACASTTTGCTTCCT | 93664 |
rs78304715 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122610162 | GTAATAAAAAAAAAA[A/G]AGAGCACTGGGGGCT | 93664 |
rs78311517 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122332341 | TGTAATGTGGAAAGA[C/T]GATCCTTGGTTCTTC | 93664 |
rs78323099 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | CADPS2 | GRCh38.p7 | 7:122582232 | ATTCACCATTTTCAC[A/G]GAGCTGTCTACATTT | 93664 |
rs78331593 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122486291 | GGAAAGGATTCATCA[C/T]TCCAAATGCCATTAA | 93664 |
rs78347737 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | CADPS2 | GRCh38.p7 | 7:122364897 | AAGGCAGAAGTGTTA[C/T]GGGCAGTGTAGACAG | 93664 |
rs78369874 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122801787 | TTATTTATTTTTTTT[C/T]TCTGGAGACATGGTC | 93664 |
rs78380347 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | CADPS2 | GRCh38.p7 | 7:122827335 | CCCTAGATGGTTTCA[A/G]AGAAAATTCTAGTAA | 93664 |
rs78388126 | snp | G/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122466389 | AGGCTCCTGCTTTTC[G/T]CTGTCTTTGCCACTC | 93664 |
rs78391111 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | CADPS2 | GRCh38.p7 | 7:122601765 | AAGAAAAAATATTGC[C/T]GTTATCATCCAGGTC | 93664 |
rs78408922 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122584799 | AATTTCTCTCTATAT[A/G]TATCTTTTCCTTTTT | 93664 |
rs78417792 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122740791 | GTTCATTTCTAACCA[C/T]ATAGAGAGTTCCTAG | 93664 |
rs78427312 | snp | G/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122852287 | TACCTGAATTCAACT[G/T]TTCATTCAACTACAA | 93664 |
rs78427700 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CADPS2 | GRCh38.p7 | 7:122377491 | GTAATTGAATGATGC[C/T]GATTATGCAAACTTC | 93664 |
rs78435752 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122520717 | AGATTGTTCAAAGAA[C/T]ACTTCAACACACACA | 93664 |
rs78449978 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122868011 | AATCTCTTCCTGCTA[C/G/T]AAGGGTGTGAGACTT | 93664 |
rs78454820 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | CADPS2 | GRCh38.p7 | 7:122648869 | ACCAGGCCCACAAGC[A/C]AAAGATCTACAGCAG | 93664 |
rs78465230 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122786664 | TACTGTTACGAGTTT[C/T]GTGTTTAAGACAGGA | 93664 |
rs78471487 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122666051 | CTCATCTAATCACTC[A/T]TTGAGCAGTGACATT | 93664 |
rs78473951 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122336407 | AAACATTGCAGTGAT[C/T]AACTGATAGAAATGC | 93664 |
rs78478145 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122621073 | ATCATGACTGGATAA[A/T]TTTTTTTTTTTAGAA | 93664 |
rs78482462 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122450362 | GTGGTGACATTTTAT[A/G]GGCCTAATAATAAGG | 93664 |
rs78485161 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122405671 | CTCAAACAAAACAAA[A/C]AAAAAACCGGCTTAG | 93664 |
rs78492252 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122564662 | TCCAGCAATCCCACT[A/G]CTAAGTACCCAAAGT | 93664 |
rs78492771 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122594908 | GGAAAGAATAAGTAA[C/T]TGATGTATAACTTAA | 93664 |
rs78510147 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122333228 | TATTGCTTTTTAAAT[A/C]CATAATGTAGGATTT | 93664 |
rs78516677 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122355797 | AGCTTATTCACTCAT[C/T]TTATAGATGACTAGA | 93664 |
rs78516916 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122656696 | AAAGAGCTGCAGGAT[A/G]TAGACTTTCCCTGGG | 93664 |
rs78518134 | snp | A/C | 0.0337553 | 0.125452 | intron-variant | CADPS2 | GRCh38.p7 | 7:122833521 | CCCGTCCTCCCACCA[A/C]ACCCAGCTTTGTTTT | 93664 |
rs78521798 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122658643 | AACATGCAGTGTTTG[A/G]TTTTCTGTTCCTGTG | 93664 |
rs78522364 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122415652 | ATTACCCCTTGGTTT[A/G]GGAAATAAAAATATC | 93664 |
rs78542667 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | CADPS2 | GRCh38.p7 | 7:122598919 | GAGCAAACAGTGAGA[A/G]TTCTGGGGACTGAGA | 93664 |
rs78554795 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | CADPS2 | GRCh38.p7 | 7:122670942 | CCTTGCTGGATCTCC[A/G]TGCTCCAGTCCCACA | 93664 |
rs78558191 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122596288 | CAGGAGCTCCATCAA[G/T]AATTTAAAGGGGTGG | 93664 |
rs78565000 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122768245 | TTTCCTACCTTCATT[C/G]CATCTTCATTTCCTA | 93664 |
rs78570909 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122644809 | AGCAACACATTCCCT[C/G]TGTGAAGTTATGTAT | 93664 |
rs78588237 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122558817 | TGAGGCCAAACTACA[C/T]ACATTTGTGCATAAA | 93664 |
rs78593990 | snp | A/C | 0.0788843 | 0.182262 | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122703773 | GAGCTTAGGCAAAAG[A/C]AGATAGTGGCTTGGA | 93664 |
rs78594907 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122612673 | CTGGTAATCTTTGCA[C/T]AATCTTTACAAAAGT | 93664 |
rs78600050 | snp | A/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122790397 | GCCAGACAGCGTTTC[A/T]AAAAAAAAAAAAAAA | 93664 |
rs78610067 | snp | A/T | 0.0232847 | 0.105357 | intron-variant | CADPS2 | GRCh38.p7 | 7:122784188 | TAAGCTCAGTTTTTT[A/T]AAATATTGTTTATTT | 93664 |
rs78633424 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | CADPS2 | GRCh38.p7 | 7:122386092 | GTCATTATTTAAGGT[A/G]TAAGTATTTAGTGTT | 93664 |
rs78634253 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122780927 | TGTATTCTTATTTAA[C/G]GCTGCTTTTATTCTA | 93664 |
rs78635001 | snp | A/T | 0.0236746 | 0.106192 | intron-variant | CADPS2 | GRCh38.p7 | 7:122717023 | AATATCCCAACAAAA[A/T]TTGCCACTTAGAACT | 93664 |
rs78635673 | in-del | -/CC/CCA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122780894 | ACTACAAACAATGCA[-/CC/CCA]AAAATCACTCTTACA | 93664 |
rs78641167 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | CADPS2 | GRCh38.p7 | 7:122744300 | ACTGCAACCCTAGAC[A/C]ACCTACCTCCCAACT | 93664 |
rs78649203 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122575191 | AGTAAAAAAAAAAGG[A/T]GGTGGGAGCATCTAA | 93664 |
rs78657201 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122757696 | CTAGCTGAGTTTTTT[A/T]AAACAACTGACTAAC | 93664 |
rs78661139 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | CADPS2 | GRCh38.p7 | 7:122623824 | AACAAAGAAAAAGGC[A/G]AGCATGTCACGTATC | 93664 |
rs78663048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122855864 | GTGACTTAACTCTCA[C/T]TCCAAATCCCTTCTC | 93664 |
rs78666096 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122378897 | TCGCTTTCATCAAAG[A/G]TATTTTGAGCATCAA | 93664 |
rs78677569 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | CADPS2 | GRCh38.p7 | 7:122488993 | GAAAACATCAGAATG[C/T]GCTCTTTTTATTTTA | 93664 |
rs78695918 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122631705 | TTTTCTTTTTTTTTT[A/T]ATTTCAGATTTGGAG | 93664 |
rs78707934 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | CADPS2 | GRCh38.p7 | 7:122748023 | TAGGATGCAGATTTC[C/T]TCAACGCAGATGCCA | 93664 |
rs78709274 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122800506 | CTTCTTAAAATTGAG[A/T]TTCTAAAGTAGTAGA | 93664 |
rs78719566 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | CADPS2 | GRCh38.p7 | 7:122604700 | TTACCTTCTTCACTC[A/G]TTTTTAAGTGGTCAC | 93664 |
rs78720439 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | CADPS2 | GRCh38.p7 | 7:122446495 | TCTATAGATTATAGT[A/G]CTCTACTGATACCCA | 93664 |
rs78724484 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122668447 | AAAGAGTCAAGACAA[A/T]ATCTTCTGAAATGCC | 93664 |
rs78740606 | snp | G/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122493738 | TTTTTTTTTTTTTTT[G/T]GCCAATTTTGATGAG | 93664 |
rs78742486 | snp | A/C | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122799605 | CCAGATTCCATCTCA[A/C]AAAAAAAAAAAAAAA | 93664 |
rs78743810 | snp | G/T | 0.0722614 | 0.17581 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122538215 | AACTGATTTAATGAG[G/T]TTAATATACCTTTGA | 93664 |
rs78748359 | snp | C/T | 0.368119 | 0.220336 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122552065 | ACTGAGAAAACAGAA[C/T]AGATGCTTAGGTTAA | 93664 |
rs78762429 | snp | A/G | 0.219947 | 0.248187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122639495 | CGTAATCACCCATCT[A/G]ATTCACATTTCCTCA | 93664 |
rs78765967 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | CADPS2 | GRCh38.p7 | 7:122789475 | TTGCAAGGGATATCT[A/G]TTAAGGAATATAAAA | 93664 |
rs78774747 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | CADPS2 | GRCh38.p7 | 7:122723457 | GGCCATCAGAGAAAT[A/G]CAAATCAAAACCACA | 93664 |
rs78789241 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | CADPS2 | GRCh38.p7 | 7:122600018 | TATATCTTAATTCAC[A/G]TAAGTGGTGCTATAA | 93664 |
rs78790792 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | CADPS2 | GRCh38.p7 | 7:122741006 | AATACTACAGATACA[A/C]CTGCACATGTGAGAA | 93664 |
rs78798263 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122744513 | ATTTCATATGAAAAA[C/T]TCCTTATCCAATAAA | 93664 |
rs78832865 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122704363 | TAGACTTTTTTTTTT[C/T]CATGTTCAAATGGAG | 93664 |
rs78851204 | snp | A/G | 0.0644444 | 0.167538 | intron-variant | CADPS2 | GRCh38.p7 | 7:122434241 | ATTTTTCTCTAAAGT[A/G]CACTTAGCAATCATT | 93664 |
rs78853506 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122525509 | AGGCTGGAGGAACTG[A/G]GCAGTAAGATACGCT | 93664 |
rs78865330 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122812284 | TCTGGTTAGCTATAA[A/T]GTTGTAAAACTTTGA | 93664 |
rs78871266 | snp | A/G | 0.0711525 | 0.174681 | intron-variant | CADPS2 | GRCh38.p7 | 7:122429815 | TCAGAGAAAACTGTT[A/G]TATCATCTTAGAAAT | 93664 |
rs78882463 | snp | A/C/T | 0.0142994 | 0.0835679 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122556416 | CACCAACTTTAAAAA[A/C/T]ATTATTTGGCATGAG | 93664 |
rs78891823 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | CADPS2 | GRCh38.p7 | 7:122605700 | AAAAATCACTGAATT[A/G]AGTTTTTATTAGACA | 93664 |
rs78892926 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122414695 | AAAGCAGATGTTTTG[A/T]ATAATCATATTTATA | 93664 |
rs78893623 | snp | G/T | 0.0528381 | 0.153711 | intron-variant | CADPS2 | GRCh38.p7 | 7:122348079 | TGAAGAACAGACAAA[G/T]GGGACGCTTGTCTTT | 93664 |
rs78916281 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122392404 | GTTTTTTTTTTTTAA[A/T]TCATCACAAAAACAT | 93664 |
rs78925489 | snp | C/G | 0.0633504 | 0.166319 | intron-variant | CADPS2 | GRCh38.p7 | 7:122489933 | TGAAAAATTAGATAA[C/G]TGATTATGTGACTAC | 93664 |
rs78944505 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122422811 | AAAAAAAAAAAAAAA[A/T]AGCCTGGCGTGGTGG | 93664 |
rs78944661 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122674174 | ACGCTGTCCTGCAAG[C/T]GCCCCGCACAGCCCC | 93664 |
rs78960414 | snp | A/C | 0.0644693 | 0.167566 | intron-variant | CADPS2 | GRCh38.p7 | 7:122346662 | TTTCCTATGTACAGC[A/C]GAAGATGTGGATTAA | 93664 |
rs78963739 | snp | C/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122882431 | ATAATGAAAAGAGCA[C/G]TGACTAGAAACCTAT | 93664 |
rs78966774 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | CADPS2 | GRCh38.p7 | 7:122677387 | AAGGGGGCCTTAAGG[C/T]AGCTCCCTGGGCTGC | 93664 |
rs78967084 | snp | C/T | 0.378174 | 0.214642 | intron-variant | CADPS2 | GRCh38.p7 | 7:122574786 | ACAGACTATAACACA[C/T]AAATTTTTTTTAAAT | 93664 |
rs78982374 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | CADPS2 | GRCh38.p7 | 7:122606127 | TACATCATCAATCAA[C/T]CACTTCCTCAAAACC | 93664 |
rs78987519 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | CADPS2 | GRCh38.p7 | 7:122792056 | GAACCTCAAAGGCAA[A/G]CTCAGTATTGCCAAT | 93664 |
rs78994566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122664258 | ATATGTAATTTTTAC[C/T]CAAAATTGCCCAACA | 93664 |
rs78996821 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CADPS2 | GRCh38.p7 | 7:122506428 | GCATCACTGCTTTTG[A/G]TAGGGCACCTAAGTT | 93664 |
rs78999004 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | CADPS2 | GRCh38.p7 | 7:122518637 | CTGTATTCTCCCTCA[A/G]TATTTTGTAACCTGC | 93664 |
rs79023629 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122632319 | TAATTTGGATTACCA[A/C]CCACAGAATACAAAC | 93664 |
rs79028065 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122575188 | AAAAGTAAAAAAAAA[A/G]GGTGGTGGGAGCATC | 93664 |
rs79036861 | snp | A/C | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122742391 | CAGAGACTCCATCTC[A/C]AAAAAAAAAATTAAT | 93664 |
rs79044122 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122329682 | CAATTAAATATAACA[C/T]GTATTGCCTGGAAAC | 93664 |
rs79046186 | snp | A/C | 0.00144961 | 0.0268831 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698462 | AGTTACCAATCATAA[A/C]CACAACGACATCTTC | 93664 |
rs79047527 | snp | A/G | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122861351 | TACTCAACATCGTTA[A/G]TTATCAGGGATATGC | 93664 |
rs79056628 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122561332 | CCTTCCTTCTATACA[C/T]TTTTTTTTTTAAACA | 93664 |
rs79060029 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122864383 | TACTTGGGAGGCTGG[A/G]TCAGGAGGATTGTTT | 93664 |
rs79060556 | snp | C/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122822398 | GCTTAATCTCTCCCA[C/G]TCTAGGTTCCCACGC | 93664 |
rs79066769 | snp | A/T | 0.0681886 | 0.171594 | intron-variant | CADPS2 | GRCh38.p7 | 7:122663818 | TAAGATGGTTTACTT[A/T]GACCTGTATGTCTCC | 93664 |
rs79067864 | snp | G/T | 0.0410537 | 0.137264 | intron-variant, upstream-variant-2KB | CADPS2, LOC105375481 | GRCh38.p7 | 7:122529801 | ATTCCTGGGTATGAG[G/T]TTTGATTCAATTGCT | 93664 |
rs79068323 | snp | A/C | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122848769 | CGTCTCTGACTTTTT[A/C]CCCAAGAGTTTCAGA | 93664 |
rs79081910 | snp | C/T | 0.193966 | 0.243639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122359254 | GAAGAGAGATTAGAA[C/T]GAGGATTAATGGGTA | 93664 |
rs79095937 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122550886 | TAGTTTCTATAATTA[A/G]TTTAGATGACATATT | 93664 |
rs79122703 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122373254 | CAGAGCAGTGTTTCT[C/T]AAAGTCTGGCTCATG | 93664 |
rs79149968 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | CADPS2 | GRCh38.p7 | 7:122391018 | TTGGTAGGCAGGGAT[A/G]TATCTTCAAAACCAT | 93664 |
rs79159456 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122654377 | ACTGAGAAGAAGTCA[A/G]TGCCTGGTTTCAAAG | 93664 |
rs79165162 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122372059 | TCTATCTGTATTAAC[A/T]TACTTACTATTCACT | 93664 |
rs79176290 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122545547 | TGGGAAGCAACTGAA[A/T]TTTTTTTTTAGTAGA | 93664 |
rs79176824 | snp | A/C | 0.0275645 | 0.114116 | intron-variant | CADPS2 | GRCh38.p7 | 7:122843815 | TGGGCAGATGAGTCT[A/C]CATGATGAAATGGCA | 93664 |
rs79185122 | snp | C/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122679278 | CCTGGGGGGGGGGGG[C/G]TCTAAAATGGCCACC | 93664 |
rs79193547 | snp | A/C | 0.031825 | 0.122064 | intron-variant | CADPS2 | GRCh38.p7 | 7:122746659 | CACACACACACACAC[A/C]CCCTCATGTTTTAAA | 93664 |
rs79235625 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | CADPS2 | GRCh38.p7 | 7:122322799 | ATAAGTGTCTTTGTT[A/T]AGGGTAAAGTTGGCT | 93664 |
rs79236934 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122335359 | GGATCAAGTGATTCT[A/C]CTGCCTCAGCCTCCC | 93664 |
rs79262084 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122374066 | CCATCACCAAATGAG[A/T]TTGATCCCTAGGATC | 93664 |
rs79265584 | snp | A/C | 0.0535932 | 0.154675 | intron-variant | CADPS2 | GRCh38.p7 | 7:122477572 | CAAAAAACAAAAAAC[A/C]AAAAACTGTAAAGTG | 93664 |
rs79272486 | snp | C/G | 0.0505692 | 0.150756 | intron-variant | CADPS2 | GRCh38.p7 | 7:122494076 | TGACTTTAAGTAAAG[C/G]AGATTATCGTCGATA | 93664 |
rs79283113 | snp | A/C | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122415603 | GCAAATACAGAACCA[A/C]AAAAAAAAAAAAAAA | 93664 |
rs79291503 | in-del | -/AAA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122506741 | TTAAAAAAAAAAAAA[-/AAA]CAAACAAACTACACC | 93664 |
rs79297981 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122448458 | AGGATTGTATAGTAC[A/C]TATTTAGAGAAATTA | 93664 |
rs79305097 | snp | C/G | 0.039522 | 0.134904 | intron-variant | CADPS2 | GRCh38.p7 | 7:122498140 | TTTAATAGAGACGGG[C/G]GTTCACCACGTTGGC | 93664 |
rs79305257 | snp | A/C | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122752657 | CCTACCTTTGCCTAC[A/C]AAAATGCCTAGTGTT | 93664 |
rs79314101 | snp | A/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122793412 | CTTTTGATCTTTGTT[A/T]GTTTAAAGTCTGTTT | 93664 |
rs79329489 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122420508 | GGTTTCACCCATTTG[A/G]CTAAGGCCAAGAAGT | 93664 |
rs79333983 | snp | C/T | 0.20511 | 0.245937 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122546287 | ATAGGGGGCTGTGGC[C/T]GTGATATTATACCCT | 93664 |
rs79358240 | snp | A/C | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122393078 | AATAAAAAAAAAAAA[A/C]CAGTATTCCTCAACC | 93664 |
rs79367622 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | CADPS2 | GRCh38.p7 | 7:122785485 | AGGCATTAGTACTTA[C/T]GTAAATACCCCAGGT | 93664 |
rs79370233 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | CADPS2 | GRCh38.p7 | 7:122859976 | AAGTTGAAATGCAGA[C/T]AAAAACATCCCTTTG | 93664 |
rs79374667 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122616893 | TAACCATATTAATTA[A/G]AAGGCAACTACACTT | 93664 |
rs79375435 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122483168 | TGTGTCTCAGAACAA[G/T]CATTTTTATGAAGAA | 93664 |
rs79377101 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | CADPS2 | GRCh38.p7 | 7:122473004 | CAAAAGTCCCAGACC[C/T]GGGAAGCTCCAAAAT | 93664 |
rs79384673 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122846961 | CTGACCCAGTATGCC[C/G]GGCAGCAGATCCAGG | 93664 |
rs79399015 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | CADPS2 | GRCh38.p7 | 7:122843233 | ACACATCATAAGAGT[C/T]GCTTTTTTTTTTGGC | 93664 |
rs79400731 | snp | C/T | 0.155987 | 0.23165 | intron-variant | CADPS2 | GRCh38.p7 | 7:122642832 | AATCCTAGTTAACTG[C/T]ACTCTTCCTTCTCCT | 93664 |
rs79402294 | snp | A/T | 0.0659589 | 0.169201 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122557615 | AGGGCCACTGCTAGC[A/T]GTGACACAGATATTG | 93664 |
rs79410071 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122371995 | TTAGAGGAACAATAA[C/T]AACAATATCAACTAA | 93664 |
rs79429453 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122348337 | GAAGAGTTTATTTTC[C/T]ACCACCTGAAACTAA | 93664 |
rs79429623 | snp | C/T | 0.0980852 | 0.198549 | intron-variant | CADPS2 | GRCh38.p7 | 7:122679540 | ACCTTGTGATCTCAC[C/T]CTGACCTTCTGCCTT | 93664 |
rs79456163 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | CADPS2 | GRCh38.p7 | 7:122726615 | TTAGCAAACGACATG[C/T]ACGAAACTGACTTAA | 93664 |
rs79459039 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122662396 | TTTTTTTTTTTTTTT[A/T]AGACGAGTCTTACTT | 93664 |
rs79461623 | snp | A/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122610443 | TAAGCAAAAAAAAAA[A/T]TCCAGATACAAAGAC | 93664 |
rs79473972 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122804000 | AAAAAAAAAAAAAAC[A/T]CTGCAAAGCACACTC | 93664 |
rs79485660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122495753 | CAATTTGTACATACT[A/G]TATATACCTGTGGTA | 93664 |
rs79494691 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | CADPS2 | GRCh38.p7 | 7:122641832 | AGTAACTACAAAAGT[C/T]GTGGCTCTCCAGGAG | 93664 |
rs79519010 | snp | A/G | 0.0360663 | 0.129354 | intron-variant, nc-transcript-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122543004 | CCATCTAAGTGACTT[A/G]GGGCAACACTATCAT | 93664 |
rs79529189 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122652252 | CTCTCTCTCTCTCTA[C/T]ATATATATATATGCT | 93664 |
rs79530173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122382595 | TTGATAGGTTTTTTT[C/T]CCCATTTAGTATAAC | 93664 |
rs79562476 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | CADPS2 | GRCh38.p7 | 7:122415107 | CTCTAGATCTTTAGT[A/G]AATGTTAATATGTAA | 93664 |
rs79565496 | snp | C/T | 0.135484 | 0.22223 | intron-variant | CADPS2 | GRCh38.p7 | 7:122350307 | AGTAAAAATTTATAA[C/T]TGATCATAGAACATA | 93664 |
rs79567739 | snp | C/G | 0.111224 | 0.207945 | intron-variant | CADPS2 | GRCh38.p7 | 7:122397658 | AGACACTGTCAAAAG[C/G]CCCTCTTAATATGTA | 93664 |
rs79578012 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122812958 | TTCTCTATGGGCTGT[A/T]TGCCAATTGGGCCTT | 93664 |
rs79599031 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | CADPS2 | GRCh38.p7 | 7:122473523 | TATTCCAAAATCTGA[A/G]GAAAATTCAATATTT | 93664 |
rs79609502 | snp | A/C/G | 0.00875054 | 0.0656008 | intron-variant | CADPS2 | GRCh38.p7 | 7:122333334 | GAATGAGCTGTTAGC[A/C/G]TGTCTTTCTGCTTCA | 93664 |
rs79625128 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122684692 | GATGGGTGATATGCC[A/C]ATGTTAACAAGGAAG | 93664 |
rs79641398 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122785215 | TTTTCAAATGTTCAC[A/G]TCTCCTCCAACATTG | 93664 |
rs79644746 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122369142 | TCCCCCCCCCCCCCC[C/T]TTTTTTTTTTTTTGA | 93664 |
rs79655621 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122661116 | TAAAAAGGAATACTA[C/T]ATCACGATAAAGGAG | 93664 |
rs79659934 | snp | G/T | 0.0433465 | 0.140692 | intron-variant | CADPS2 | GRCh38.p7 | 7:122356356 | TTTAGAGGAAGACCA[G/T]AGAGGTAAAGTGCCA | 93664 |
rs79682191 | in-del | -/TT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122331167 | TCTGTTATTTTTTTT[-/TT]AACTTATTCATCTGG | 93664 |
rs79686025 | snp | G/T | 0.5 | 0 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122552974 | TCACTGAACTTGTCA[G/T]CATCAGCTAAAACTC | 93664 |
rs79705077 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122789007 | AAGAGGAAGCAGTAC[C/T]TGACCTCTGTAACTC | 93664 |
rs79710330 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122655707 | CTTGCATAGCATTCA[A/G]GAAAAAAAAAGTGTC | 93664 |
rs79715242 | snp | A/C | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122380115 | CTTTAAATAAATACC[A/C]AAAAAAGATGTATTT | 93664 |
rs79718053 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122807302 | CCAGTGATCATATCC[C/T]CAGTGCCTGAATCCC | 93664 |
rs79728567 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | CADPS2 | GRCh38.p7 | 7:122643401 | CTCCCTACTCTCTCA[C/G]CCCACAAACACATGA | 93664 |
rs79769016 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | CADPS2 | GRCh38.p7 | 7:122414738 | ATTTATAACCAGATA[C/T]AATAAATCTTAGTTA | 93664 |
rs79777588 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122888517 | GTGGTTATTAAGTCA[A/G]AGATCTCCAAGCCTT | 93664 |
rs79781984 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | CADPS2 | GRCh38.p7 | 7:122660997 | ATGTTAAAAGTAAAC[A/G]GATGGAGAAAGAGAT | 93664 |
rs79784430 | snp | G/T | 0.00597247 | 0.0543191 | utr-variant-3-prime | CADPS2 | GRCh38.p7 | 7:122319684 | AATTAAGTACAAAAC[G/T]AACCTGGCACATAAA | 93664 |
rs79797270 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122705245 | GAGTCTTCCTGGAAC[C/T]GCATGTGACTGGGAG | 93664 |
rs79797983 | snp | A/G | 0.021333 | 0.101051 | intron-variant | CADPS2 | GRCh38.p7 | 7:122712645 | GACCAGAGAAGCACA[A/G]TATCTTAGTCTGTTT | 93664 |
rs79802304 | snp | C/T | 0.430884 | 0.172571 | intron-variant | CADPS2 | GRCh38.p7 | 7:122822414 | TCTAGGTTCCCACGC[C/T]GCCCCTAATCCTGCT | 93664 |
rs79812475 | snp | A/G | 0.134802 | 0.221877 | intron-variant | CADPS2 | GRCh38.p7 | 7:122664229 | TAAGTCTAATATCCA[A/G]GTCAATATTCATCAT | 93664 |
rs79828080 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122771825 | GTGGGTACCTGACAA[C/T]AGTCCAAGCTGGAAA | 93664 |
rs79846825 | snp | A/T | 0.0505692 | 0.150756 | intron-variant | CADPS2 | GRCh38.p7 | 7:122478387 | GTGATGATTAACCTA[A/T]GGACTAACTACAGAT | 93664 |
rs79849585 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | CADPS2 | GRCh38.p7 | 7:122434341 | TGAAAAAGGTAGGGG[A/G]AAAAAAAAAGAAAGA | 93664 |
rs79855284 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122585463 | CCACTCAACAAAGGA[A/G]AAAAAAAAAAAAAAG | 93664 |
rs79861592 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122382026 | TATAGGCACATGAGT[G/T]TGAGAGAAAAGATGG | 93664 |
rs79875316 | snp | A/C | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122670872 | GAAACCCTGTTTCAA[A/C]AAAAAAAAAAAAAAG | 93664 |
rs79917810 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122655709 | TGCATAGCATTCAGG[A/G]AAAAAAAAGTGTCTT | 93664 |
rs79921945 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CADPS2 | GRCh38.p7 | 7:122757469 | GTTTTTTAAAGCATT[C/T]TGTACTACAATAAAT | 93664 |
rs79924252 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | CADPS2 | GRCh38.p7 | 7:122883252 | AGCTCTAATAGTGAA[C/T]GGGCTTTGACTAAAG | 93664 |
rs79928323 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122441868 | GGGTCATGAGTAAAG[C/T]GATAATATGCATTCT | 93664 |
rs79928621 | snp | A/T | 0.0644693 | 0.167566 | intron-variant | CADPS2 | GRCh38.p7 | 7:122345945 | TTTGTTAAATGGCTA[A/T]CTTGAAAGGCCAGTA | 93664 |
rs79940747 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122729084 | CATGTGATCAACTCT[C/T]TTAGATTCTACATAT | 93664 |
rs79949581 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | CADPS2 | GRCh38.p7 | 7:122342842 | AAGTTCGTCATGATG[C/T]CTGAATGAAATTTTT | 93664 |
rs79957936 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122793339 | AGCAAGAAGAGCTAA[C/G/T]TATCCTAAATATATA | 93664 |
rs79972805 | snp | C/G | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122793395 | AATGGCCTTCTTTGT[C/G]TCTTTTGATCTTTGT | 93664 |
rs79976660 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122398774 | TCTCTCCCGCCGCCC[C/T]CCCCACCCCTCACCC | 93664 |
rs80051466 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122590380 | TTAATGGGATATCCA[A/T]ATTGTTCTATAACAT | 93664 |
rs80051566 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122369065 | TGGTAAGATTTAATG[C/T]TCCTATTTTTTTTCC | 93664 |
rs80080582 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122655632 | GTGTGACCTGCTTTA[C/T]TGCAATATTCACTTT | 93664 |
rs80098625 | in-del | -/CC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122328559 | GGTCTACACAGGAAT[-/CC]AAAGCAGTAAGTGTA | 93664 |
rs80104099 | snp | A/C | 0.0663309 | 0.169604 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539850 | CTTTAGTAAAGCATG[A/C]TTTAATTTTATGCAA | 93664 |
rs80104398 | snp | A/G | 0.277778 | 0.248452 | intron-variant | CADPS2 | GRCh38.p7 | 7:122818642 | ATAGGGTGGAGGAGC[A/G]GAGGCTGAGGGAGAA | 93664 |
rs80111806 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | CADPS2 | GRCh38.p7 | 7:122381821 | TACAATGTTAAAAAC[A/G]AAGGAATAAAGAAGT | 93664 |
rs80131835 | snp | A/C | 0.0648419 | 0.167978 | intron-variant | CADPS2 | GRCh38.p7 | 7:122381573 | TTGAATTGATTCTGG[A/C]AAATCTTAAAATCAA | 93664 |
rs80131900 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122583483 | TTTTCAGCATTTTAC[A/C]TTTAAGTGTGATAAC | 93664 |
rs80141549 | in-del | -/ATTT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122757167 | AGTTTTTATTTATTT[-/ATTT]TGAGACAGGGTCTTT | 93664 |
rs80141791 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | CADPS2 | GRCh38.p7 | 7:122731183 | GAACATAAACAAATG[A/G]AAACAGTAAGAAAAC | 93664 |
rs80145894 | snp | A/C | 0.0482946 | 0.147699 | intron-variant | CADPS2 | GRCh38.p7 | 7:122463987 | ACCTAGCTCTGTCCA[A/C]CTGAGAGGGCCTGGA | 93664 |
rs80149952 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122759779 | AAGCAACTTATCATC[A/G]TAATTTGATTTTAAC | 93664 |
rs80151186 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | CADPS2 | GRCh38.p7 | 7:122726041 | TATTCAAGACAGTAA[A/C]TTTTAACTCACCAGC | 93664 |
rs80151793 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | CADPS2 | GRCh38.p7 | 7:122750700 | GAAAGAAGAACAAGT[A/G]AACAAATCCCAAAGC | 93664 |
rs80171020 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122462655 | ACAAGAATATAGAAA[A/G]GCTAACGATGTGAAC | 93664 |
rs80199945 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | CADPS2 | GRCh38.p7 | 7:122494737 | CCTTAATGGGAGAGA[C/T]TGAGGCCAGTATCTT | 93664 |
rs80201768 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | CADPS2 | GRCh38.p7 | 7:122462601 | TCATATTGAAAAATT[A/T]AATCAAAATCTAGTT | 93664 |
rs80206565 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CADPS2 | GRCh38.p7 | 7:122421579 | AAACATTTTATTCCA[C/T]GTAAGGTACTTCGCT | 93664 |
rs80215237 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122341974 | TTTCTGTTTTAAGCA[A/G]AAAGTGTTTTGTAAA | 93664 |
rs80222787 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122847654 | AAGATACTAAGCTTA[C/T]GGCGTGGGAAAACTT | 93664 |
rs80225592 | snp | C/G | 0.0704125 | 0.17392 | intron-variant | CADPS2 | GRCh38.p7 | 7:122870773 | AAAAAGAGATTAAAA[C/G]CGCTATCTTGTCCAT | 93664 |
rs80231141 | snp | G/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122664086 | AAAAAAAAAAAAAAA[G/T]ATGATTAGGAAAACA | 93664 |
rs80233480 | in-del | -/ATTT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122526209 | TTTATTTATTTATTT[-/ATTT]GAGGCAGAGTCTCAC | 93664 |
rs80236211 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122606015 | GATTAATAAGCAAAA[A/G]CTCTTTCAATTATTT | 93664 |
rs80236888 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | CADPS2 | GRCh38.p7 | 7:122687122 | CTAAATACTTTTTAC[A/G]CAAGGGAGCTACTAG | 93664 |
rs80237513 | in-del | -/ACT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122729698 | TTTTTTTTTTTTTTT[-/ACT]GTTGAGTCCTTTGAG | 93664 |
rs80239665 | snp | A/C | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122800991 | AGCGAGACTCTGCCT[A/C]AAAAAAAAAAAAAAA | 93664 |
rs80247140 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122695968 | CAAGTACCCCACACA[A/C]GAGTACACAGAGCTG | 93664 |
rs80248385 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122724420 | TCCTGCTCTGAAGCA[A/G]CTTATAATTATCACA | 93664 |
rs80261602 | snp | C/G | 0.0399052 | 0.1355 | intron-variant | CADPS2 | GRCh38.p7 | 7:122631261 | ATATTTTTCTCACAG[C/G]TTCAACAAAAAATAG | 93664 |
rs80264890 | snp | A/C | 0.0298908 | 0.118541 | intron-variant | CADPS2 | GRCh38.p7 | 7:122691202 | TATGACGACTGTAAC[A/C]CATTCTGCCACACTC | 93664 |
rs80268295 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122395317 | TTTTTCTACCTCTAA[C/T]TGATATGGGTTAGTA | 93664 |
rs80282647 | snp | A/C | 0.0486741 | 0.148216 | intron-variant | CADPS2 | GRCh38.p7 | 7:122360408 | ATTCTTTAACTGGTT[A/C]ATCTTTATCATTATT | 93664 |
rs80295625 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | CADPS2 | GRCh38.p7 | 7:122409076 | GAAAATTGAGCATAC[C/T]GTTTTTTGCATATAT | 93664 |
rs80300884 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122356335 | TTAGACTGCAGTTAC[A/G]AGATTTTTAGAGGAA | 93664 |
rs80318430 | snp | G/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122787867 | CCATCTGATTCTTCA[G/T]CCTCATTAAATAGGC | 93664 |
rs80319677 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122791341 | AAAGATACACACACA[C/T]ACTTCTTAAACCTTG | 93664 |
rs111203896 | snp | A/G | 0.165527 | 0.235296 | intron-variant | CADPS2 | GRCh38.p7 | 7:122645467 | TATGTATATATGTGT[A/G]TATATGTATATATAT | 93664 |
rs111231616 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122388264 | AGACCTTTTTCATAC[A/G]TCTCAGGAGATATTA | 93664 |
rs111236935 | snp | G/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122411399 | CTAATTTTGTATTTT[G/T]AGTAGAGATGGGGTT | 93664 |
rs111237275 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122401798 | GGCCAGAAATGGAGG[C/T]TGACTTTGTTTTCAT | 93664 |
rs111242771 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122349769 | AGAGAAAAAAATTCC[A/T]TGTTAATTATATGCT | 93664 |
rs111246508 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122619354 | TTATAGACTAGGCAC[A/G]GTGTCTCAAGCCTGT | 93664 |
rs111247332 | in-del | -/A | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122594278 | AGTCTCAAAAAGGGG[-/A]AAAAAAAATTACAAG | 93664 |
rs111254901 | in-del | -/A | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122669355 | TATATATATATATAT[-/A]TTTTTTTTTTTTGAG | 93664 |
rs111257126 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122646343 | TGCCGTCAAAGAGGC[A/T]TATGTAAACATCAAT | 93664 |
rs111266160 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122561519 | GAAAAGTAAGATGTG[C/T]CAATCATTCTCCAGT | 93664 |
rs111268020 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122559232 | GAAAAATAAAGATAT[A/G]GGGGCTGTTGAAACC | 93664 |
rs111280461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122645209 | ACATATATGTATATA[C/T]ATAAGTATATATATA | 93664 |
rs111282596 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122705525 | TCTATATTTATATTG[C/T]GTATTATCTATATTA | 93664 |
rs111284250 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | CADPS2 | GRCh38.p7 | 7:122654889 | CATTAACACACTTGT[C/G]ATTCAAGGGAGGAAG | 93664 |
rs111286169 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122471713 | TTCATGAAGAGCTAA[C/T]GTCATCAATTTTGAA | 93664 |
rs111293131 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122553669 | TTTGAATCATCAGTT[C/T]GCTCCACCCTGATGT | 93664 |
rs111296675 | in-del | -/CAAA | 0.0850919 | 0.187897 | intron-variant | CADPS2 | GRCh38.p7 | 7:122619626 | CAGTCTCCAAACAAA[-/CAAA]TAAATAAATAAGATA | 93664 |
rs111297352 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122433008 | AGACAGGGTCTCCTT[C/T]TGTCACCCACGCTGG | 93664 |
rs111337734 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122732910 | TTATATAATATACAT[G/T]ATATATTATGTATAA | 93664 |
rs111346213 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122572968 | CAAACAAAATTTGCA[C/T]GCCAAGTACTTGCCA | 93664 |
rs111376647 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122474220 | AGCAATCAACTGGAA[G/T]CCTTTATCCCTCACT | 93664 |
rs111376674 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122784579 | CAGGAAAATGATATA[A/C]GTTGAAAGTAAGATT | 93664 |
rs111385579 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | CADPS2 | GRCh38.p7 | 7:122833292 | TTTTTCACCATATTG[C/T]TATTGTAAATCAATT | 93664 |
rs111392362 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122412857 | GAAGGAAGAGAATGA[C/T]AGAATGGAAAGGGAC | 93664 |
rs111394163 | snp | A/C | 0.039522 | 0.134904 | intron-variant | CADPS2 | GRCh38.p7 | 7:122423071 | TCTAATTTGAATCTT[A/C]ACTCTGATATCAACA | 93664 |
rs111407754 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122571159 | TTCAAAAATGAGAAA[A/G]CAAGCAACCCAGTTA | 93664 |
rs111408630 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122677844 | GAAGGGCCAATGAGT[A/G]AATGGATTGGTAAGG | 93664 |
rs111409521 | in-del | -/GA | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122516924 | GTATAGTTTACATAA[-/GA]AGTAAAATTACCTGT | 93664 |
rs111465006 | snp | C/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122441335 | CAGAAAGGCTTCAGG[C/G]AGAATGAAGTGCTGT | 93664 |
rs111487418 | in-del | -/AT | 0.124125 | 0.215999 | intron-variant | CADPS2 | GRCh38.p7 | 7:122366669 | TACATACACACATAC[-/AT]ATATATATATATACG | 93664 |
rs111492457 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122742078 | ACAGATGCGCAGAGT[C/T]GCTATTATAGCTTTT | 93664 |
rs111505043 | in-del | -/T | 0.097727 | 0.198275 | intron-variant | CADPS2 | GRCh38.p7 | 7:122625054 | TATGATGATTAATTA[-/T]TTTTTTTTTTTTTGA | 93664 |
rs111509412 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122617361 | TGGCCTTAATAATTA[C/G]TGATAAAGACAGCCA | 93664 |
rs111518246 | snp | G/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122485765 | TGCCATCCAGGACTT[G/T]CGCAGTTAGAGAGAA | 93664 |
rs111558104 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122383098 | GGTGTCCATCAATGG[C/T]AGACCAGATAAAGAA | 93664 |
rs111559108 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122820663 | CTCCCGGGTTCACGC[A/C]ATTCTCCTGCCTCAG | 93664 |
rs111561709 | snp | C/T | 0.312593 | 0.242037 | intron-variant | CADPS2 | GRCh38.p7 | 7:122819919 | GCCAATATCCCATCC[C/T]GCAGCATGCTTTAAA | 93664 |
rs111562428 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122690823 | TTTAGCTCATTAGCT[A/T]CTTTGCCCACACTTG | 93664 |
rs111588386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122873882 | CATGAGATGATATCT[C/T]GTTGTGGTTTTGATT | 93664 |
rs111596787 | snp | C/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122651704 | GGTAAATCTGGGTGA[C/G]TCGCTTTCTTCAGTT | 93664 |
rs111602852 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122587738 | TTTATATTCCTTTGG[A/G]TATATAACCAGTAAT | 93664 |
rs111611954 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122361903 | ACATGGAGAAACCCC[A/G]TCTCTACTAAAAGTA | 93664 |
rs111615060 | snp | A/C | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122723589 | CTGGTGGGATGGGAA[A/C]CTAGTTCAACCATTG | 93664 |
rs111615580 | in-del | -/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122744971 | TACATCTCATTTTTC[-/T]TTTTTTTTTTTACTT | 93664 |
rs111633362 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122467151 | CACATGGCATAAAAC[C/T]TGTCAGATCAGGTAC | 93664 |
rs111640700 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CADPS2 | GRCh38.p7 | 7:122624610 | TAAATGTTTTTGCTA[C/T]AAATTAGAGCAGATT | 93664 |
rs111647064 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122602317 | GTCAATCTTCATCTT[-/A]CGACCATTGCAATTT | 93664 |
rs111649798 | snp | A/T | 0.0543475 | 0.155628 | intron-variant | CADPS2 | GRCh38.p7 | 7:122677446 | GGGAGGTGCCTGAGG[A/T]GGACGGGTGGGCTTT | 93664 |
rs111654027 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | CADPS2 | GRCh38.p7 | 7:122508167 | TGAAATGGAGTCTTG[C/T]AGAACAATTTTCAAA | 93664 |
rs111657638 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122654100 | CACCAAACAGCCAAA[C/T]TGAAGGCTATGAGAA | 93664 |
rs111660026 | snp | A/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122335367 | TGATTCTCCTGCCTC[A/T]GCCTCCCGAGTAGCT | 93664 |
rs111667123 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122749764 | AACAAATTTACATTA[A/G]CAAATTCAAGGATTT | 93664 |
rs111688547 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122501251 | CAGAGTGAACTCTGT[C/T]TCAAAAACAAAACAA | 93664 |
rs111693344 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122793882 | TATTTCCTCTTCACT[C/T]ATGAGGCTTACTTTG | 93664 |
rs111699560 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122850057 | TTGATGATGAAGACC[C/T]GGGGGCCTTGCTTGG | 93664 |
rs111710952 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122774049 | GAAAAATCAGTGTAG[C/T]TCAGAGACACTAAAG | 93664 |
rs111713459 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122654762 | GGAATTTTGACTTTC[A/G]AGTCTTATTATTTAA | 93664 |
rs111719766 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | CADPS2 | GRCh38.p7 | 7:122662628 | ATCTGCCCGCCTCAG[C/G]CTCCCAAAGCATTGG | 93664 |
rs111724131 | snp | C/G | 0.0611083 | 0.163768 | intron-variant | CADPS2 | GRCh38.p7 | 7:122404651 | ACATCCTCTCCAGCA[C/G]CTGTTGTTTCTTGAC | 93664 |
rs111732752 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122709981 | GTTAATGGGTGCAGC[A/G]CACCAGCATGGCACA | 93664 |
rs111737124 | in-del | -/TT | 0.0962929 | 0.197165 | intron-variant | CADPS2 | GRCh38.p7 | 7:122512749 | TTATATGTATTATGC[-/TT]TATATATAAAATATA | 93664 |
rs111746084 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122690763 | ACAGCTGCAGATTAC[A/T]GTAGGTGTCACCTTC | 93664 |
rs111746477 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | CADPS2 | GRCh38.p7 | 7:122658305 | TGGGACTGTAAACTA[C/G]TTCAACCACTGTGAA | 93664 |
rs111762990 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122884470 | CCAATTTGTTTGGGA[C/T]TGGGAAATGCTATTA | 93664 |
rs111768445 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122345218 | GCAACCTCTGCCTTC[C/T]CGGCTCAAGCGATTC | 93664 |
rs111774133 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122478417 | TGTGGGATTGGTAAT[G/T]GAGGATACTGGTGGA | 93664 |
rs111781403 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122432643 | AAGACTCTGTTAAAA[A/T]AAAAAAAAAAAAAAA | 93664 |
rs111822215 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122610376 | AGTTAATTGATCTCA[C/T]GAACCAAATATTTAA | 93664 |
rs111827947 | snp | A/T | 0.0244538 | 0.107838 | intron-variant | CADPS2 | GRCh38.p7 | 7:122768742 | CATATGTTTAGGTTT[A/T]TAAGCAAATATTTTC | 93664 |
rs111829736 | snp | A/T | 0.378174 | 0.214642 | intron-variant | CADPS2 | GRCh38.p7 | 7:122574446 | GTGAGACCCTGTCTT[A/T]AAAAAAAAAAAAAAA | 93664 |
rs111834058 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | CADPS2 | GRCh38.p7 | 7:122789397 | AATTAGTAGTAAGAG[C/T]TGCTATTTAATTCCC | 93664 |
rs111858230 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122378487 | TAAATTATTAATGAG[C/G]ATTAACATTTTTCAT | 93664 |
rs111867689 | snp | A/C | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122422958 | AGTGAGACTCCGTCT[A/C]AAAATAAATAAATAA | 93664 |
rs111876507 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | CADPS2 | GRCh38.p7 | 7:122383354 | AGGGAGGGAGGGAGA[C/T]GTGGATGGAAAAACG | 93664 |
rs111879290 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122568793 | AAGATTTCTTAGATA[C/T]AGCACCAAGAACCTG | 93664 |
rs111898661 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122592130 | TACAAAGAACTCAAA[A/C]AAATTTACAAGAAAA | 93664 |
rs111901548 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | CADPS2 | GRCh38.p7 | 7:122880617 | GTACACTGAAATCAA[C/T]TGGGAAGTTTTAACA | 93664 |
rs111913539 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122635003 | CTTTTATTGCCCTGT[C/T]GTCCAAAAGGATGCT | 93664 |
rs111916762 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122599321 | CCAAACCAGAGAGAG[A/G]CTCCTGAAATAAACC | 93664 |
rs111943235 | in-del | -/C | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122812886 | TACAAACTTACTCTA[-/C]AGAACCAACATTACT | 93664 |
rs111944740 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | CADPS2 | GRCh38.p7 | 7:122327951 | ATAAGAAAAAATTAT[C/T]CTATCAAATAAGAAC | 93664 |
rs111964885 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | CADPS2 | GRCh38.p7 | 7:122646332 | AGTTGTTAAAATGCC[A/G]TCAAAGAGGCATATG | 93664 |
rs111971280 | snp | C/G | 0.0948562 | 0.196037 | intron-variant | CADPS2 | GRCh38.p7 | 7:122681252 | CCTGCACAATGTGCA[C/G]ATGTACCCTAAAACT | 93664 |
rs111993729 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122422792 | AAACCCCGTCTCTAT[A/T]AAAAAAAAAAAAAAA | 93664 |
rs112011234 | snp | A/T | 0.470132 | 0.118498 | intron-variant | CADPS2 | GRCh38.p7 | 7:122527621 | GAGAGAGAGAGAGTG[A/T]GTGTGTGTGTGTGTG | 93664 |
rs112021824 | snp | A/C | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122696505 | TAGTCTTCCATGACC[A/C]CATGGTCATGGAAGC | 93664 |
rs112042201 | snp | A/G | 0.0952156 | 0.196321 | intron-variant | CADPS2 | GRCh38.p7 | 7:122479945 | AAGACAAATGCTACT[A/G]TTCATATTGTATTAT | 93664 |
rs112047381 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122483559 | ATAACATGTACATAA[C/G/T]GGACATGTACAAAAT | 93664 |
rs112048087 | in-del | -/G | 0.229723 | 0.249176 | intron-variant | CADPS2 | GRCh38.p7 | 7:122671648 | TTGTGAGAAGCAGCT[-/G]ATCAACTGCCCGGAG | 93664 |
rs112049664 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122699680 | ACTTCTGCCTCACTT[C/T]CTCTGTCTTACATTG | 93664 |
rs112057965 | snp | A/G | 0.487241 | 0.0788465 | intron-variant | CADPS2 | GRCh38.p7 | 7:122591539 | GCCAAGACAATCCTA[A/G]GCCAAAAGAACAAAG | 93664 |
rs112076339 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122658658 | CCAAACACCACATGT[C/T]CTCACTCATAGGTGG | 93664 |
rs112085042 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122623332 | TAAAAAACATATTTT[-/A]CGTTTTTGGACTAAC | 93664 |
rs112097553 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122563218 | ATAGACAGGAAAGCA[C/T]CACTATTCTTGATCT | 93664 |
rs112105786 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122775140 | CATTCTGGGTACACC[A/G]TGTCTTTTATCCAAT | 93664 |
rs112112751 | in-del | -/A | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122871184 | TGCCACAGTGCTGGG[-/A]AAAAAAAAAAAAATT | 93664 |
rs112118611 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | CADPS2 | GRCh38.p7 | 7:122644099 | GAAGGAAGGAATGAA[G/T]GAAGGAAGGAAGGAA | 93664 |
rs112122647 | snp | G/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122354580 | CAAAACTTTTTTTTT[G/T]GGGGGGAGGGGTTAG | 93664 |
rs112136994 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122360238 | GTTTACCATGTGAAC[A/G]TTCTCATTGTAGCTA | 93664 |
rs112137698 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122879553 | AATAAAAAATAAAAA[A/T]AAAAAAAGAAAAGAA | 93664 |
rs112139602 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122705530 | ATTTATATTGTGTAT[G/T]ATCTATATTATATAT | 93664 |
rs112150609 | in-del | -/GAA | 0.378765 | 0.214288 | intron-variant | CADPS2 | GRCh38.p7 | 7:122582093 | GACTCAGCACAGCAT[-/GAA]GAAGATGCCATTGAG | 93664 |
rs112156879 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122542308 | CTTTAGTAAATTTTA[A/T]TTATGTATTAACATT | 93664 |
rs112162142 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122842941 | TCAAAGCCTTTCAGT[A/G]ACCACAATACTAGGA | 93664 |
rs112164408 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122884409 | GGCTCATAAAAACAC[C/T]GCGGGGCATTCAAAA | 93664 |
rs112193370 | in-del | -/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122524318 | TAGGCCTTCATTTCC[-/T]TTTTTTTTGGAAATG | 93664 |
rs112193765 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122400405 | TCACTCCATTGCACT[A/C]CAGCCTGGGCAATAA | 93664 |
rs112196785 | snp | C/G | 0.0322114 | 0.122752 | intron-variant | CADPS2 | GRCh38.p7 | 7:122401859 | AGTCTGTGAGGGGTG[C/G]GACATTGGGGACAGT | 93664 |
rs112200408 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | CADPS2 | GRCh38.p7 | 7:122477279 | GCACTTTGGGAGGCC[A/G]AGGTGGGTGAATCAC | 93664 |
rs112201903 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, downstream-variant-500B | CADPS2, RNF133 | GRCh38.p7 | 7:122697457 | AGTAATTTTCTTACC[A/G]AAATAGAACCCAATA | 93664 |
rs112210315 | snp | G/T | 0.291493 | 0.246533 | intron-variant | CADPS2 | GRCh38.p7 | 7:122649962 | CAGCGCAGGCTGGAG[G/T]GCAGTGGTGTGATCT | 93664 |
rs112214037 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122638940 | CACGAGAGCAGTACA[C/T]ACTAGCTCCTCTAGT | 93664 |
rs112214892 | in-del | -/C | 0.298398 | 0.245271 | intron-variant | CADPS2 | GRCh38.p7 | 7:122786111 | AACTTCTAGTAGTCT[-/C]CGTCTATTTCATATA | 93664 |
rs112220038 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122683776 | AGATTCCCAGTTGGG[A/G]CTGCTGTCTGTGTGG | 93664 |
rs112246605 | snp | C/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122494838 | ACTTTTTCCCTTGCA[C/T]ATGTCTAAGGTTTAC | 93664 |
rs112250758 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122810135 | GTCTGTCCTTGAAAC[C/T]AGGTTTGGAAAATGT | 93664 |
rs112260653 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122438674 | AATGTAATCCTCCCA[C/T]CTTAGCTCCTCCTAA | 93664 |
rs112267157 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122470789 | GTGTAAGCCACCACA[C/T]GCGGCATGATATGGA | 93664 |
rs112271284 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122501901 | AAAAAAAAAAAAAGG[A/G]AAAAAAAAGTCACCT | 93664 |
rs112287747 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122561138 | ACAGACACAGTGCTC[-/T]TTTTGTATACTGAAA | 93664 |
rs112290645 | in-del | -/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122433407 | TTTGTGTTTTTTTGG[-/T]TTTTTTTTTTTTTGA | 93664 |
rs112294846 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122360722 | TTTGAAATAAACCCA[C/T]GATGAACTGCAATTT | 93664 |
rs112298446 | snp | C/T | 0.0839998 | 0.186933 | intron-variant | CADPS2 | GRCh38.p7 | 7:122673140 | GACCTTCGCTGTGAG[C/T]GTTACAGCTCTTAAA | 93664 |
rs112310189 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | CADPS2 | GRCh38.p7 | 7:122351804 | AGGTAGTCATATTAC[G/T]TTTATTCTTAACAGT | 93664 |
rs112339629 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122721068 | GTGGGCATCATCACA[C/T]TCAAGTCCTCTAGGT | 93664 |
rs112344439 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | CADPS2 | GRCh38.p7 | 7:122507658 | AGCAGCAAATTGTCA[C/T]AATGTGAGTTATGCT | 93664 |
rs112350018 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122805121 | GCTAACCCCCAGCAA[C/G]GTACCCTGATAAATG | 93664 |
rs112353591 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122444280 | ATGAGCAATCATATA[A/G]AAGTCTGTGTGGACA | 93664 |
rs112361478 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122766702 | GCTCAAGCAGTGGCT[A/G]TTTTAAAAACTTTTT | 93664 |
rs112378045 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | CADPS2 | GRCh38.p7 | 7:122378987 | CTCTGTCTCTGAGAA[C/T]AGATCTAGAGCCTTA | 93664 |
rs112388365 | snp | G/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122807527 | CTGAAACCCAGCCTC[G/T]GGAGGCGGCTCCCCT | 93664 |
rs112389932 | snp | A/G | 0.0876345 | 0.190099 | intron-variant, upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122623423 | GATCCTTTCAATGTC[A/G]TATGGAGGTGAAGGC | 93664 |
rs112399631 | in-del | -/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122356306 | TTGAGATATGTCTGA[-/T]TTTTTTTTGATGATT | 93664 |
rs112402311 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122674388 | TGTCACCTTTCACTA[C/T]GTATGTCACATTTGT | 93664 |
rs112403918 | snp | C/G | 0.5 | 0 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122532028 | AGAGCAAGACTCCGT[C/G]TCAAAAAAAAAAAAA | 93664 |
rs112404543 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122732564 | ATATATATTGTTGAA[G/T]AATATAATATAATAT | 93664 |
rs112412602 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122449483 | ACCACACCCAGATAA[C/T]TTTTTAGTTTTTCTT | 93664 |
rs112422482 | snp | A/T | 0.0256215 | 0.110247 | intron-variant | CADPS2 | GRCh38.p7 | 7:122492198 | AATGAATAAATAAAT[A/T]AATTAATTAATTAAT | 93664 |
rs112426728 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122711705 | TCACCCAGGATGGAG[A/T]ACAGTAGCGTGATCT | 93664 |
rs112434947 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122420055 | GAGAGGTTGAAGGTG[A/C/T]CTGAGGTTATACAGT | 93664 |
rs112435936 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122850539 | CAATATCTGTATCTC[A/T]CCCTCTTTTTGGAGG | 93664 |
rs112436223 | snp | A/C | 0.0726307 | 0.176182 | intron-variant | CADPS2 | GRCh38.p7 | 7:122455870 | CACCACCACACCTGG[A/C]TAATTTTGTATTTTT | 93664 |
rs112457742 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122465951 | ATAACACCTATGTAC[A/G]TATAGAGCTTTCTTT | 93664 |
rs112468818 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122356917 | TTTCTCCAATGAGCC[C/T]TGGTTCATTTCATTA | 93664 |
rs112470310 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122612812 | GGTAGAGCAATGGTA[A/G]TCCAGAAAGTGTGGT | 93664 |
rs112472299 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122616473 | TGTAAATATGAATGT[A/G]TATTTGTTTTTTGTT | 93664 |
rs112484154 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122589690 | GGGAAATTCAAGTGC[C/T]TGATTCCAATAGGCT | 93664 |
rs112498545 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122737482 | TCCCAGTGTGCTGGG[A/T]TTACAGGCATGAGCC | 93664 |
rs112513492 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122841617 | CCTCAAGCTTTGCCG[C/T]AAGAGTAGGAGAAAA | 93664 |
rs112526710 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122876073 | TGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCTGA | 93664 |
rs112530002 | in-del | -/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122519864 | AATTGATTTTTTTTT[-/T]AAAGGAAATGGCCAG | 93664 |
rs112531243 | snp | C/T | 0.13446 | 0.221699 | intron-variant | CADPS2 | GRCh38.p7 | 7:122433659 | CCACCCATTTTGGCT[C/T]CCCAAAGTGCTGGAA | 93664 |
rs112532888 | in-del | -/A | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122418170 | GGGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 93664 |
rs112546296 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122566433 | TATATCCAAAGGAAA[C/T]GAAATCTGTATATAG | 93664 |
rs112551175 | snp | A/G/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122650739 | AATAAAGCCTATAAT[A/G/T]TAATTTGTTAGGAAT | 93664 |
rs112562629 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122821238 | CTTGATTTATTGATG[A/G]CGGTTCCACCAGGCC | 93664 |
rs112563119 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122748171 | CAAAGACTCCAGCAC[C/T]GAAGCAAGTGAGTGA | 93664 |
rs112567752 | snp | G/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122568929 | AGCCAATATCATATT[G/T]AATGGGCAAAAACTG | 93664 |
rs112569684 | snp | A/C | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122773034 | AAAGTTAATAACTTT[A/C]TTAGAGTTAGATCTC | 93664 |
rs112571793 | snp | A/G | 0.134802 | 0.221877 | intron-variant | CADPS2 | GRCh38.p7 | 7:122452491 | ACCTCCGCCTCCTGG[A/G]TTCAAGCAATTCTCC | 93664 |
rs112572320 | snp | G/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122679267 | AAGAATGCATTCCTG[G/T]GGGGGGGGGGCTCTA | 93664 |
rs112572747 | in-del | -/AT | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122645248 | TATATATACACACAT[-/AT]GTACATGTGTGTATA | 93664 |
rs112577400 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122682915 | ACTGGCCACTCCTCA[C/T]GAGAGAGAACATGCA | 93664 |
rs112596329 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122656132 | TTGAAAAATTACTAT[A/G]AGCTGGGTGCAGAGA | 93664 |
rs112598883 | snp | A/G | 0.119978 | 0.213528 | intron-variant | CADPS2 | GRCh38.p7 | 7:122452500 | TCCTGGATTCAAGCA[A/G]TTCTCCTGCCTCAGC | 93664 |
rs112632743 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122617351 | AAAACATAGGTGGCC[C/T]TAATAATTAGTGATA | 93664 |
rs112642504 | in-del | -/AT | 0.239202 | 0.256839 | intron-variant | CADPS2 | GRCh38.p7 | 7:122670177 | TTATTGTCAATTGGC[-/AT]ATATATATATATAAA | 93664 |
rs112663366 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122806256 | TGTTCACTTTAGAAT[C/G]AATAAATCAGTATTG | 93664 |
rs112663724 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122760452 | AGAGTCAACAGCAAC[A/T]AAATTTTGGAAACTG | 93664 |
rs112678668 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122801349 | ATATGTATTAAAAAA[A/C]CTCCTAAAGAAATCT | 93664 |
rs112693462 | snp | A/C | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122461845 | GTGATCCACCCGCCT[A/C]GGCCTCCCAGAGTGC | 93664 |
rs112700984 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122468151 | ACAGCACTGTTGTCC[C/T]TCACTTCAGTCAATA | 93664 |
rs112702101 | snp | C/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122434902 | TGGTCCTCTTTTCTT[C/G]TTGTAAGAGCCCTTC | 93664 |
rs112705643 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | CADPS2 | GRCh38.p7 | 7:122495925 | AGAATATTCTCTTCT[G/T]TTTATTAGTCACTTG | 93664 |
rs112706398 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122706797 | GTACATACATATATA[A/T]ATACACACACACACA | 93664 |
rs112707216 | snp | C/G/T | 0.00716521 | 0.0594565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122742704 | ACTTCTAAAACATTC[C/G/T]TACATGTGCCTCAGT | 93664 |
rs112709049 | snp | A/G | 0.040671 | 0.13668 | intron-variant | CADPS2 | GRCh38.p7 | 7:122384558 | GGGAAGGCCTATGCA[A/G]TTATGTGGGTATGTT | 93664 |
rs112710934 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122672104 | ATATCTAATACTTCC[C/T]ATAATCTGTGTTCTT | 93664 |
rs112719762 | snp | C/T | 0.0944967 | 0.195752 | intron-variant | CADPS2 | GRCh38.p7 | 7:122711872 | TGGTCAGGCTGGTCT[C/T]GAACTCCTGACCTTG | 93664 |
rs112727618 | snp | C/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122334585 | AACAGAGAGCAAGAG[C/T]GTGCTCTTATCTCAC | 93664 |
rs112731929 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | CADPS2 | GRCh38.p7 | 7:122343079 | ATTTTCTAACTGTAA[C/T]TGAGGCAAATTCAGT | 93664 |
rs112732946 | in-del | -/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122621072 | ATCATGACTGGATAA[-/T]TTTTTTTTTTTTAGA | 93664 |
rs112743579 | snp | C/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122640492 | ACACACACACACACA[C/G]AGATAGAGAGAGAGA | 93664 |
rs112745275 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122871231 | CCACTTTTTGACTTA[C/T]GTATTCCAGCATTTT | 93664 |
rs112751048 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122576773 | GTCTCAGGAGATCTG[A/T]TTTTTTTTTTTTTTT | 93664 |
rs112755028 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | CADPS2 | GRCh38.p7 | 7:122676917 | TTTGTGCCAGGCTTT[C/T]TATCCATCCAAGTCT | 93664 |
rs112757393 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122730973 | GTTCCCCAAATTTCA[C/T]AATAAACATATTGAA | 93664 |
rs112761573 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122735634 | ACAATGATAGTACAA[A/T]GAACTCCCTCATCCC | 93664 |
rs112787572 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122836810 | ACAGAGAGACTTAGA[C/T]TCTCACACAATAATA | 93664 |
rs112791647 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122394147 | TCAATTTTGCATATC[C/T]GTATTTAAAAACAGC | 93664 |
rs112795995 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | CADPS2 | GRCh38.p7 | 7:122580674 | ATGAAGAGGTGACTA[C/T]AGGAAAAGAATAATG | 93664 |
rs112804288 | snp | C/G | 0.189576 | 0.242588 | intron-variant | CADPS2 | GRCh38.p7 | 7:122587769 | GGATTTCTGGTTCTA[C/G]GTCTTTGAGGAATCG | 93664 |
rs112823319 | snp | G/T | 0.190833 | 0.242898 | intron-variant | CADPS2 | GRCh38.p7 | 7:122569905 | ATTAAAGACTTAAAC[G/T]TTAGACCTAAAACCA | 93664 |
rs112823956 | snp | C/G | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122803778 | TACAAGTCAAATGCA[C/G]ATAGCTATCAAAACA | 93664 |
rs112838947 | snp | A/C | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122442371 | TGAACCAGATTCAGC[A/C]AAGTGCCTCCTCCCA | 93664 |
rs112846533 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122426632 | AGAAACCTGTCAGTT[C/T]TCATCACTCTAGTTT | 93664 |
rs112848871 | in-del | -/AAAA | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122467072 | AGTTTTTGATAAAAT[-/AAAA]AAAAAAACTCCTCCA | 93664 |
rs112861615 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122672308 | AGCTGGTCTCCAGGC[A/G]TCGGTGGTCACCCTC | 93664 |
rs112862926 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122638376 | AGGGTGAAGTTGAAT[C/T]CTGCCCAGTTAGGAG | 93664 |
rs112866749 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | CADPS2 | GRCh38.p7 | 7:122853673 | ACAAATGAATGTACA[C/T]GTATGTAACTGTTTA | 93664 |
rs112868031 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122324707 | TTGTTTAAATAAATA[A/G]GTGATTCTCAATAGC | 93664 |
rs112879394 | snp | C/G | 0.162253 | 0.234095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122670760 | CCTGCCTCAGCCTCC[C/G]AAAGTGCTGGGATTA | 93664 |
rs112889293 | in-del | -/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122635272 | TTAATGTGTGGCTAA[-/T]TTTTTTTTTTAATTA | 93664 |
rs112891927 | in-del | -/GT/GTGT | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122433147 | TTGGCTATTTGAGGC[-/GT/GTGT]GTGTGTGTGTGTGTG | 93664 |
rs112893233 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122585665 | TGTGTTGACTCAAAA[C/T]GTATTGCCTTTCTCC | 93664 |
rs112901687 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122818222 | CCCTTGGCCTCTGTT[C/T]TCAAAAACTTAAAAC | 93664 |
rs112903160 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122823618 | TGATCTTGCCTGTCC[A/G]TAGACTTTCAGTAGC | 93664 |
rs112904720 | snp | G/T | 0.5 | 0 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122542650 | ACTTTCCTGTTTTAT[G/T]GTAGCTCTCTGATTC | 93664 |
rs112907276 | snp | A/C | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122696506 | AGTCTTCCATGACCC[A/C]ATGGTCATGGAAGCA | 93664 |
rs112914659 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122678853 | GGACCTCGAATGGAG[C/G]GACCAGCTGAAACCA | 93664 |
rs112915548 | snp | C/T | 0.0948562 | 0.196037 | intron-variant | CADPS2 | GRCh38.p7 | 7:122487008 | AGTGTAGTATAAACA[C/T]AACTTTTTTTTTTTT | 93664 |
rs112921133 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122706438 | TCAAGGAATATATAT[A/G]TATGCTTATATATTC | 93664 |
rs112939124 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122822976 | AAGCCTGTTTGGTGG[C/T]CTCTTCACATGGACA | 93664 |
rs112947685 | snp | A/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122384568 | ATGCAATTATGTGGG[A/T]ATGTTTACTGGAGAG | 93664 |
rs112960401 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122664958 | GCCTGGGCTAGTTTT[C/T]GTATTTTTTTTTTTT | 93664 |
rs112961046 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122483101 | TTGGTCTTCCCTAAC[A/G]AAACTTGAAAGCAAA | 93664 |
rs112968822 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | CADPS2 | GRCh38.p7 | 7:122658790 | CCTAATGTAAATGAT[A/G]AGTTAATGGGTGCAG | 93664 |
rs112969775 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122329858 | AGGGTTTATATATCA[C/T]GGCTGCTTCAAGCAA | 93664 |
rs112974514 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122587101 | TTTTCATGCTGAATT[G/T]TTTTTTTTTACTTTT | 93664 |
rs112986687 | in-del | -/A | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122323895 | TATATATATATATAT[-/A]TATATATATATATAT | 93664 |
rs112996987 | in-del | -/AA | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122477544 | ACCCCCGACCCCACC[-/AA]AAAAAAAAAAACAAA | 93664 |
rs113001406 | snp | C/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122424032 | CTGAACTGATTGCCA[C/G]ATAGGATAGTGTCCA | 93664 |
rs113010339 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122630579 | TTTGGAGTTAGTTCC[C/T]ACAACAATGGGACTT | 93664 |
rs113016030 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122640761 | ATGGTGAAACCACGT[C/T]TCTACTAAAAAAAAT | 93664 |
rs113021488 | snp | A/T | 0.0391387 | 0.134304 | intron-variant | CADPS2 | GRCh38.p7 | 7:122519934 | GCAAATAGTATATTT[A/T]AAAAATCTTCTATAT | 93664 |
rs113042149 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122669917 | TGACAGATCCCAGTT[G/T]CCATCCTCGAGAGGC | 93664 |
rs113058752 | in-del | -/T | 0.0970103 | 0.197722 | intron-variant | CADPS2 | GRCh38.p7 | 7:122506172 | ATAGACAACAGGTGG[-/T]TTTGACCTATTCTGA | 93664 |
rs113066775 | snp | C/T | 0.0948562 | 0.196037 | intron-variant | CADPS2 | GRCh38.p7 | 7:122711758 | CCAGGGTTCAAGCGA[C/T]TCTCCTGCCTCAGCC | 93664 |
rs113076802 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122550499 | CAGACTTCTCATAGA[A/T]CATGGTCATAATGCT | 93664 |
rs113077130 | snp | G/T | 0.0349115 | 0.127424 | intron-variant | CADPS2 | GRCh38.p7 | 7:122719225 | ACAGAGGGGAAAGGA[G/T]AAGTGAGGAAAGGAA | 93664 |
rs113078322 | in-del | -/CA/CACA | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122564847 | ACATACACACACATG[-/CA/CACA]CACACACACACACAC | 93664 |
rs113088225 | in-del | -/TACA | 0.382279 | 0.212137 | intron-variant | CADPS2 | GRCh38.p7 | 7:122607047 | AACTACAAAAGCACC[-/TACA]TACATAGACATTTCA | 93664 |
rs113101622 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122583623 | CATATGATATATACA[C/T]AATATATAAAAAATA | 93664 |
rs113106758 | in-del | -/CAC | 0.330947 | 0.236533 | intron-variant | CADPS2 | GRCh38.p7 | 7:122780892 | TGACTACAAACAATG[-/CAC]CAAAAATCACTCTTA | 93664 |
rs113108847 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122363389 | TAGTGAGTCTGTGCA[C/T]ACACACATGTGTGTT | 93664 |
rs113114188 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122589552 | CTTATATAACACTAA[C/T]GTACTTCAGCCAAAG | 93664 |
rs113124249 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122624072 | TGAATTTTTTTCTCC[A/G]AAAAAGCTCAAAATT | 93664 |
rs113127267 | snp | A/G | 0.0114905 | 0.0749213 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698017 | ATCCCCAAAACTTTA[A/G]GAATATCACATTTGC | 93664 |
rs113140509 | snp | A/C | 0.00569822 | 0.053072 | intron-variant | CADPS2 | GRCh38.p7 | 7:122663194 | ACTTCATGTTCATTC[A/C]ACGAGTCAGACAGGG | 93664 |
rs113143625 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | CADPS2 | GRCh38.p7 | 7:122637570 | TTGGGCTGTTTTACG[C/G]AATTCCTTGAATACC | 93664 |
rs113151680 | snp | C/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122403402 | AAATCTGCAAATCAC[C/G]ATAAAATAAAAGCCA | 93664 |
rs113152661 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | CADPS2 | GRCh38.p7 | 7:122716693 | CAATTAAAAATAAAT[A/T]AATAAATAAGAAAGG | 93664 |
rs113157386 | in-del | -/A | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122619460 | TTTACTAAAAAATAC[-/A]AAAAAAAAAAAAAAA | 93664 |
rs113167242 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | CADPS2, RNF133 | GRCh38.p7 | 7:122697718 | CACACTTCAAACAGA[C/T]AAACTGCTTGTCAGT | 93664 |
rs113187024 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122760836 | GGGAGGGGGGCGGGA[C/T]AGCATTTGGAGATAT | 93664 |
rs113197000 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CADPS2, RNF148 | GRCh38.p7 | 7:122701296 | TCCTTTGTAGGGACA[C/T]GGATGAAGCTGGAAA | 93664 |
rs113216094 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122432614 | CCAGTGCACTCCAGC[C/G]TGGGCAACAAGGCAA | 93664 |
rs113219901 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122590015 | CACCAAAACATTTCC[C/T]TATTTAAGATGTTTG | 93664 |
rs113223661 | snp | C/T | 0.21845 | 0.248001 | intron-variant | CADPS2 | GRCh38.p7 | 7:122722267 | gtccctgtttgcaga[C/T]gacatgattgtatat | 93664 |
rs113234255 | snp | G/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122524077 | ACTTATGCAATCCTA[G/T]ACATTTTTGTGAGAT | 93664 |
rs113237308 | snp | C/G | 0.392881 | 0.205147 | intron-variant | CADPS2 | GRCh38.p7 | 7:122592180 | AAAGTGGGCGAAGGA[C/G]ATGAACAGACACTTC | 93664 |
rs113247902 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122511082 | GAATAAATTCAAATT[C/T]ATTATAGTTTGGTGG | 93664 |
rs113250672 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817884 | ACCTCTTATCTCTGC[A/G]CCCCAATCCCTTATC | 93664 |
rs113279345 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122434394 | TTCAGTTAAAAACAA[C/T]CCAAGCAAACTTGCT | 93664 |
rs113288263 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122565988 | CCTACTCTCTGCTTC[C/T]AAGAGTTTGGCCTTT | 93664 |
rs113296018 | snp | A/G | 0.000115412 | 0.00759556 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698111 | TACAAGTCAGAATAC[A/G]AACTATGTCATTAGG | 93664 |
rs113311271 | in-del | -/TGTCTCAAT | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122469411 | GTCTATTTTTTGATA[-/TGTCTCAAT]TCCCCTAGTCAGAAG | 93664 |
rs113313757 | snp | C/G | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122764559 | CAGTGTGTAAACACA[C/G]TGTAAGATGGTGCTG | 93664 |
rs113320676 | snp | C/T | 0.0640965 | 0.167152 | intron-variant | CADPS2 | GRCh38.p7 | 7:122483096 | ACTGCTTGGTCTTCC[C/T]TAACAAAACTTGAAA | 93664 |
rs113324996 | snp | A/G | 0.000679106 | 0.0184144 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122663396 | TTCACCTCTGTAAAT[A/G]GCATCATATTTGGCT | 93664 |
rs113344243 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122820955 | ACAAACTATGCTCAA[C/T]TCACTCTCTACAGTT | 93664 |
rs113348305 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122491968 | ACGAGGTCAGGAAAT[C/T]GAGACCATCGTGTCT | 93664 |
rs113357730 | in-del | -/CTAA | 0.0119091 | 0.0762411 | intron-variant | CADPS2 | GRCh38.p7 | 7:122731139 | AGATTAAATACCTCT[-/CTAA]CTCTCATTTATTCTT | 93664 |
rs113358668 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122480346 | TTAGTTTTTTAAAAA[A/G]TAAGCTTCTGATTTA | 93664 |
rs113363433 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122372676 | AGAAATTCACTGTTA[C/T]TTTCATCTACTTTAT | 93664 |
rs113387820 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122734112 | AGTCAGCTATGGTGG[C/T]ATGAGGTCCTTAGCT | 93664 |
rs113388353 | snp | A/G | 0.204189 | 0.245767 | intron-variant | CADPS2 | GRCh38.p7 | 7:122564372 | GGAGTGCAGTGGCAT[A/G]ATCTTGGCTCACTGC | 93664 |
rs113389779 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122626591 | ATTTTCTAAGTAACA[A/G]TGATCACCTTCCATA | 93664 |
rs113396081 | in-del | -/A | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122496611 | TTTTTCATTTTTATG[-/A]TTTGTTTTTTATGTT | 93664 |
rs113398207 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | CADPS2 | GRCh38.p7 | 7:122592830 | CATCACACACTGGGG[C/T]CTTCCAGGGGGATGG | 93664 |
rs113422240 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122797658 | ATGAGAACACATGGA[C/T]ACCTAGAGGGGAATG | 93664 |
rs113424675 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122334740 | AATTATTAGTATCTA[C/T]TTTGAAACAGTATTG | 93664 |
rs113428939 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122540764 | TTCTTCTTTCTTCTC[C/T]TTGTCTAGTAATTTT | 93664 |
rs113431210 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122403350 | TACCTCTCTACATGG[A/G]GGAGCTGTTTTTCTC | 93664 |
rs113432594 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122408492 | TGCAGTGGGTTGATC[C/T]CAGCTTACTGCGACC | 93664 |
rs113435165 | snp | G/T | 0.205417 | 0.245993 | intron-variant | CADPS2 | GRCh38.p7 | 7:122564401 | GCAACCTCTGCCTCC[G/T]AGGTTCAAGCAATTC | 93664 |
rs113441629 | snp | A/C | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122468521 | TACTTTTTTCTTCAT[A/C]TCACAATTTACATCC | 93664 |
rs113442701 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CADPS2 | GRCh38.p7 | 7:122728898 | ATTATATTACAAGTC[A/G]CCTCTCTTCTGTTTT | 93664 |
rs113451304 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122734376 | AAAAAAAAAAAAAAA[A/G]AAAAAAAAAAGAAAA | 93664 |
rs113455380 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122565415 | AGGAAGATAGTGGGG[A/G]ATAAGGTCAGGACAT | 93664 |
rs113462759 | in-del | -/TTTTT | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122636463 | TTTCCACAAGAGATG[-/TTTTT]TTTTTTTTTTTTTTT | 93664 |
rs113479671 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122612849 | ATAAGAATAGACATA[C/T]AGATTGGTAAAACAG | 93664 |
rs113480973 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122553074 | GATAAATTTATCCTT[C/T]AAGTTTTATCTCAAA | 93664 |
rs113492888 | snp | A/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122789265 | CTATTCAGGGCTCAG[A/T]GTTTTTATACTCTTC | 93664 |
rs113503860 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122668223 | TGTGGAAATATAAGA[A/G]AGGGAAAATTGGAAA | 93664 |
rs113511258 | in-del | -/C | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122468501 | AGTCCTAACTACATA[-/C]TTTTTACTTTTTTCT | 93664 |
rs113532448 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122818935 | AAAAGGCCGTCTTAT[C/T]CTCAAAATACATTTT | 93664 |
rs113533191 | snp | C/T | 0.153332 | 0.230554 | intron-variant | CADPS2 | GRCh38.p7 | 7:122378544 | TTTCTAAACAGGATG[C/T]CTTTTGTCTGTTTAT | 93664 |
rs113534277 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122815651 | TATTGCAGCGAAACG[C/T]TAGACATCGACAAAG | 93664 |
rs113537893 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122588547 | TCTTAAAATTTAGCC[A/G]TTTTAAGATTAAAAT | 93664 |
rs113541803 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122503715 | ACTTTTTTCCTCCCT[C/T]TCATTCATTCATCCG | 93664 |
rs113579963 | in-del | -/G | 0.49931 | 0.0185575 | intron-variant | CADPS2 | GRCh38.p7 | 7:122601142 | AAGGGCATAAAAGAT[-/G]TATTTTTCATCTCTA | 93664 |
rs113593383 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122455160 | CTGGCCTCCTAACTA[G/T]TCCTCAAACACAGGA | 93664 |
rs113594790 | snp | G/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122760460 | CAGCAACAAAATTTT[G/T]GAAACTGGAAAACAC | 93664 |
rs113600383 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122452891 | CATATAATCATATGT[A/G]TGTGTGTGTGTATAT | 93664 |
rs113611370 | snp | A/C | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122713321 | CCTGTACTTAACACT[A/C]GCTCTACAACTTAGG | 93664 |
rs113614707 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | CADPS2 | GRCh38.p7 | 7:122343547 | AAGGAGAAAAAACTT[C/T]TACCTTTATAATGAA | 93664 |
rs113617206 | snp | G/T | 0.220246 | 0.248223 | intron-variant | CADPS2 | GRCh38.p7 | 7:122636531 | AGTGCAATGGTGCAA[G/T]CTTGGCTCACTGCAA | 93664 |
rs113645708 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122614754 | CTCACTAAGTATTCC[A/C]AGTCATTGTGCAGAA | 93664 |
rs113647822 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122750614 | ATTTCCACAGCAGAA[C/T]TTGACATCCTGTGCA | 93664 |
rs113677290 | snp | G/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122831522 | AATTATATCCCCAAA[G/T]GGGGAAGTACTTCAA | 93664 |
rs113679018 | snp | A/C/T | 0.5 | 0 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122562884 | ACAATAAACTGAAAA[A/C/T]TTTTTTTAAAGGTTT | 93664 |
rs113712607 | snp | A/G | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122461627 | TTAAGATGGAGTCTC[A/G]CTCTGTCACCAGGCT | 93664 |
rs113713395 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122680149 | ACACAAAAAAAGTAC[A/G]ATATCTGACCTCTGT | 93664 |
rs113714775 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122437433 | CTACCTGAATTTTGG[C/T]AAAACTATACTAATA | 93664 |
rs113728942 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122575581 | AGGTGGGATTACAGG[C/T]GTGCACCACCACACC | 93664 |
rs113731920 | in-del | -/A | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122850362 | GTCAGATCACCACCT[-/A]GGGGGGTGACACCTT | 93664 |
rs113738249 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122513018 | CAGAGGGTAAAGAGT[C/T]CAAAAGCATAAAACA | 93664 |
rs113748493 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122362150 | TGAAAGGGAGGTGGT[A/G]TAACATATGAGCTCT | 93664 |
rs113751407 | snp | A/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122586913 | GTGCTTTTAAAAATT[A/T]TTTGTCACCAAATAA | 93664 |
rs113766340 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122812391 | GGTGGAAATCATAAC[C/G]ATTAAAAACACTTGT | 93664 |
rs113767425 | snp | C/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122458593 | CCCCCTTCCTTGTCT[C/G]GATTTTGCACTGCAT | 93664 |
rs113769824 | snp | C/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122471170 | TTTCGAGTGGCTTTA[C/G]CAGCAAAAAGAAACA | 93664 |
rs113773528 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | CADPS2 | GRCh38.p7 | 7:122736871 | TCAGACCAGCAAGCT[C/T]CTTTAAAATGAGAAA | 93664 |
rs113783000 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122682249 | AGTGGAAGAAAAATC[C/T]TGTTGTTCATCATGG | 93664 |
rs113792847 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122533146 | TGTAGGATACTGGCA[A/G]TTGTCTATTTGTGCC | 93664 |
rs113798191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122484406 | GGCAATTCAGGGTAC[A/G]ATAATCTCTTCAACT | 93664 |
rs113806196 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122667597 | AGTCACAGCACCTGA[A/G]AGAGACAGGATACAC | 93664 |
rs113817056 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122825017 | AACAGAGACATTATC[C/T]AATAGCCAAAAACTA | 93664 |
rs113817189 | in-del | -/A | 0.104504 | 0.2033 | intron-variant | CADPS2 | GRCh38.p7 | 7:122425331 | ATGGTTCATGCCTGT[-/A]AATCCCTGCACATTG | 93664 |
rs113829747 | snp | A/C | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122532039 | CCGTCTCAAAAAAAA[A/C]AAAAACAAAACAAAC | 93664 |
rs113831716 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122353852 | GTTCTGCTCCCACTT[A/G]TTTTTAGTCATTGTT | 93664 |
rs113842817 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122738320 | CAGAGCCCTTCTAGG[C/G]ACTAAGCCCTGCACA | 93664 |
rs113847393 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122644361 | TCACTACCTTCATTG[A/T]CCAGGTCAATCTCCA | 93664 |
rs113848634 | in-del | -/A | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122731239 | ACAAAGCCAAGTCAC[-/A]AAATTTTTTTTTTTT | 93664 |
rs113860464 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122365334 | AGCAGCGACAGCACC[C/T]GTGGGATTAACCAGC | 93664 |
rs113862551 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | CADPS2 | GRCh38.p7 | 7:122421850 | TAAATTGCTGTGTAT[A/G]TCATATGGAGTTTTT | 93664 |
rs113866611 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | CADPS2 | GRCh38.p7 | 7:122635551 | TTTTTGTTCTTGCGA[C/T]AGTTTACTGAGAATG | 93664 |
rs113867679 | snp | C/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122369132 | AATTTTTGTTTCCCC[C/G]CCCCCCCCCCTTTTT | 93664 |
rs113871412 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | CADPS2 | GRCh38.p7 | 7:122418075 | CTCAGGAGGCTGAGG[C/T]AGGAGAATCGCTTGA | 93664 |
rs113880080 | snp | A/G | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122509668 | AATGTAATCATAGCA[A/G]TATGGCAGAGGAAAG | 93664 |
rs113910555 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122637568 | TCTTGGGCTGTTTTA[C/T]GGAATTCCTTGAATA | 93664 |
rs113911501 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122726787 | ACAAAAAAAAAAAAA[A/C]AACTATCCACATATA | 93664 |
rs113911847 | snp | A/C | 0.0633504 | 0.166319 | intron-variant | CADPS2 | GRCh38.p7 | 7:122405139 | CAAAAAACAAAAAAA[A/C]AAAACAAAACAAAAA | 93664 |
rs113912029 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122437311 | ATGAGATGGCTTTTT[G/T]GTTAATCACTCAGGA | 93664 |
rs113919666 | snp | A/G | 0.5 | 0 | downstream-variant-500B | CADPS2 | GRCh38.p7 | 7:122318105 | TGTGGGTGAAGAGTA[A/G]GGAACAAGCTTTTAG | 93664 |
rs113946600 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122651982 | CTCCTGCTCATACTC[C/T]AGTAGTCAACGATGT | 93664 |
rs113954411 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122557076 | ATAAAGGTGTGAACA[C/T]TGGCACGTGTAACAA | 93664 |
rs113965764 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | CADPS2 | GRCh38.p7 | 7:122630832 | CCAAGTTGATTTTTA[A/G]AAAACCAAATTCATT | 93664 |
rs113968350 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122746109 | TAAAAATACTTAACA[C/T]ATATTAAATGCTTTA | 93664 |
rs113969612 | in-del | -/T | 0.5 | 0 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122541514 | CCCAGCCAATTTTTG[-/T]TTTTTTTTTTTTATG | 93664 |
rs113971711 | snp | A/C | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122706949 | AACCGGAGTGGAATC[A/C]TCATGATTATCTTAG | 93664 |
rs113972497 | snp | C/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122360521 | TTTTTCTACCCCATC[C/T]TAGAGTGCTATAACT | 93664 |
rs113974925 | snp | A/C | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122335406 | GGCATGTGCCACCAC[A/C]CCCGGCTACTTTTTG | 93664 |
rs113998473 | snp | A/G | 0.030278 | 0.119257 | intron-variant | CADPS2 | GRCh38.p7 | 7:122768766 | TATTTTCTCTTTTAT[A/G]TCTTGTATTTCAGTA | 93664 |
rs114005465 | snp | A/T | 0.030278 | 0.119257 | intron-variant | CADPS2 | GRCh38.p7 | 7:122845588 | ATTCTCCTCGCTACA[A/T]CCCCTCAGGAGTCAC | 93664 |
rs114021581 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122409941 | TCTTTTGGCTTTAAT[A/G]CTAAGCCACTAATTA | 93664 |
rs114057613 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122467766 | CTTACAAAACCAAGA[C/T]GTATAACCACACATA | 93664 |
rs114062075 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122828044 | TGTGGATGTCTGATT[C/T]TCCTTTCAGTTCTAT | 93664 |
rs114069985 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122749959 | TTGTTCACCTGTGAG[A/G]TTAAAAAAAAAAAAA | 93664 |
rs114073916 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122830137 | AGTAACAGGCAGAAC[C/T]GCTATTCAAACCCAG | 93664 |
rs114097630 | snp | A/C/T | 0.0182019 | 0.0936463 | intron-variant | CADPS2 | GRCh38.p7 | 7:122441964 | TTCCTCCTGTGGCTA[A/C/T]TTGTGGTTTAGGGTG | 93664 |
rs114100627 | snp | C/T | 0.0329836 | 0.124112 | utr-variant-5-prime, upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122886666 | CCGACCCAGCGGTTC[C/T]CCAGAGCCCGCCGGC | 93664 |
rs114110848 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122608316 | ATGAATTATACTTCA[A/C]AAATAATTCTGACAT | 93664 |
rs114112837 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122580765 | TGCACTTCGGAGATA[C/T]TCTGTGATTAATCAC | 93664 |
rs114123750 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122395307 | AACAGATTTTTTTTT[C/T]TACCTCTAATTGATA | 93664 |
rs114127770 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | CADPS2 | GRCh38.p7 | 7:122452790 | TATATATAAAATAGG[C/T]AGAAACAGGAATTAT | 93664 |
rs114163074 | snp | C/T | 0.00121224 | 0.0245897 | intron-variant | CADPS2 | GRCh38.p7 | 7:122409619 | CTGTGATGAATGCCT[C/T]TTCTCCTAATGATGG | 93664 |
rs114171061 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | CADPS2 | GRCh38.p7 | 7:122390369 | CCTTCACATCCACAG[C/T]GTACAGCTTGGTAGA | 93664 |
rs114172809 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122549346 | CTAATTAATACAAAA[A/C]AATCAAGGATTGATA | 93664 |
rs114174447 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122557471 | CCTTTTTCCACGTGG[A/C]AAACTTACCCATAGC | 93664 |
rs114177446 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122682019 | TTTCTTCTAATATCA[C/G]CTAATAGCAGATCTT | 93664 |
rs114192049 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122348038 | AATACCAAGGTAGTT[A/G]GGTACAGCCCAGTTG | 93664 |
rs114217397 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122534878 | TCTGAGTATGTGGCA[A/C]TTAGCAGAACCTCTA | 93664 |
rs114238405 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | CADPS2 | GRCh38.p7 | 7:122596302 | AGAATTTAAAGGGGT[A/G]GAAATCACTGCTATG | 93664 |
rs114240171 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant, upstream-variant-2KB | CADPS2, LOC105375481 | GRCh38.p7 | 7:122529467 | AAAACTAGGGATAAA[A/G]ACTAGAAATCTGTTA | 93664 |
rs114247787 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122561982 | AACCTAAAATTAATA[C/T]TTCACTGTGGTGAAA | 93664 |
rs114251024 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122662646 | CCCAAAGCATTGGGT[C/T]ACAGGCGTGAGCCAC | 93664 |
rs114266073 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122719330 | AAGTCCCCAACACAG[C/T]CTTCCTCCCTGCTCT | 93664 |
rs114267036 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122772407 | GTGAAAAATTAATGA[C/T]AGTCCCACTGAAAGC | 93664 |
rs114272279 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | CADPS2 | GRCh38.p7 | 7:122877595 | ATCCATAATGAGATT[A/T]AAAAAGATGTCACAA | 93664 |
rs114278337 | snp | A/G | 0.0263992 | 0.111815 | upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122887362 | GTGGACATTTATTCA[A/G]CAAAGATTTGAGCGC | 93664 |
rs114279409 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | CADPS2 | GRCh38.p7 | 7:122663174 | ATCTTCATAGGCTTG[G/T]AAATACTTCATGTTC | 93664 |
rs114285450 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | CADPS2 | GRCh38.p7 | 7:122775052 | CAAAATTAACCTACT[C/T]CTAGAAGTTTTCATT | 93664 |
rs114288986 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122376980 | TCATCTCTTATAGAA[A/G]CTTGAGATGTTTGGT | 93664 |
rs114291563 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | CADPS2 | GRCh38.p7 | 7:122424988 | GCTTTTTTTAAAAAA[A/G]TTATTTTTTTGGACA | 93664 |
rs114300120 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | CADPS2 | GRCh38.p7 | 7:122502776 | ATCTTAAGTTTCACA[G/T]GTCTGAGATCATACT | 93664 |
rs114309319 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122423922 | AAAACAAAGGTGACC[C/T]ACGTAAACTTTGATT | 93664 |
rs114322349 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122670802 | CATGGTGCCCAGCCA[A/T]GAGCCCAGGAATTCT | 93664 |
rs114354478 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122516508 | ATGCCACTGCACTCC[A/G]GCCTGGGTGACAGAG | 93664 |
rs114368760 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122537253 | TTGTCCTAGGTTGTT[C/T]AGATAAGTATCTATG | 93664 |
rs114376836 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122610112 | ATTTTAAATTAAAGG[C/T]TATTTTAAATCAGAC | 93664 |
rs114384420 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122705324 | AGATCATTTATTCAA[C/T]ACATGGACATTCTTT | 93664 |
rs114386173 | snp | A/C | 0.030278 | 0.119257 | intron-variant | CADPS2 | GRCh38.p7 | 7:122751343 | ATAATGATTTAAAAA[A/C]ATCATGTCGAGGGAA | 93664 |
rs114402998 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | CADPS2 | GRCh38.p7 | 7:122719690 | GTAGAGAATCAGGTC[A/G]GCAATTAAATTCTAT | 93664 |
rs114410175 | snp | C/T | 0.030278 | 0.119257 | intron-variant | CADPS2 | GRCh38.p7 | 7:122807120 | CTCCTGCCACCCTGC[C/T]ACAAGCAGTGCATGC | 93664 |
rs114410435 | snp | C/T | 0.030278 | 0.119257 | intron-variant | CADPS2 | GRCh38.p7 | 7:122777530 | CAGTTTGGCTATGTC[C/T]CCACCCAAATGTCAT | 93664 |
rs114427797 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122359419 | CACTGAGAAGGGAAG[A/T]AAATGAACCATTTTC | 93664 |
rs114434875 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122419923 | TTTCAGTTTAGAATA[G/T]TTAACTTATTTTAAA | 93664 |
rs114436152 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | CADPS2 | GRCh38.p7 | 7:122491723 | TGATACGTTTGGGAT[C/T]ATTAGCCTATTAAGA | 93664 |
rs114438269 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | CADPS2 | GRCh38.p7 | 7:122321176 | TGATTGACTGATTGA[C/T]TGACTGATTGAGACA | 93664 |
rs114438830 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | CADPS2 | GRCh38.p7 | 7:122712232 | GGACTTCGCTATGCT[C/T]CTTCATCTTCCTACA | 93664 |
rs114441024 | snp | C/T | 0.021333 | 0.101051 | intron-variant | CADPS2 | GRCh38.p7 | 7:122382042 | TGAGAGAAAAGATGG[C/T]CCGAGAATTCCCATT | 93664 |
rs114448525 | snp | A/C | 0.0283406 | 0.115616 | intron-variant | CADPS2 | GRCh38.p7 | 7:122476526 | TTTTCTCAGGAAATA[A/C]AATTCCAAACTATAT | 93664 |
rs114452324 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122520132 | TCCATCAGAATGTTC[C/T]GTGACAGCAGGAACA | 93664 |
rs114454810 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122620493 | ATAAGCCCACATACA[C/G]ACATCATCAATGAAG | 93664 |
rs114462051 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | CADPS2 | GRCh38.p7 | 7:122667919 | ACATTCACTATAAGA[A/G]TGGGGGCCACGTGGG | 93664 |
rs114464480 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122557772 | GCTGGCTATTTGCCA[C/T]GATTCATGCTTTCAC | 93664 |
rs114472493 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122615033 | CTAGAAAGGGACACA[C/T]TAGTTCTAACACATT | 93664 |
rs114478937 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122777817 | TGAATCAATTAAACC[G/T]CTCTCCTTTATAAAT | 93664 |
rs114493705 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122795894 | GCAATATAGGGCATC[C/T]AAATAGGAAGAGAGA | 93664 |
rs114506891 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122739188 | GGAATGCCAAGAAGA[A/G]CTTCTCCTTGCAAGC | 93664 |
rs114509612 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122387647 | TACAACAGACAATGT[C/G]TAATTCTTTTATGTC | 93664 |
rs114522017 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | CADPS2 | GRCh38.p7 | 7:122462134 | AAATCTAAGCAAATA[C/T]GAAGTACAAAATAAG | 93664 |
rs114523820 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122488104 | TATGGAGAGGTAAGA[A/G]ACAAATTTATAAAAA | 93664 |
rs114524118 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122559271 | TAACAGCGGCACCCT[A/G]GAAAAAAACACATGA | 93664 |
rs114530574 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | CADPS2 | GRCh38.p7 | 7:122391729 | ATTACTTTGCAAGTT[A/G]TTCTCTTTCTTGGTC | 93664 |
rs114540326 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122354644 | TTAGTATTCCTATCC[A/G]CAAAGCTAATATGAA | 93664 |
rs114545934 | snp | C/G | 0.0626037 | 0.165477 | intron-variant | CADPS2 | GRCh38.p7 | 7:122486361 | ATTTACAGGAGTTTG[C/G]AGGAAGTTGATTCCA | 93664 |
rs114565334 | snp | C/T | 0.00388317 | 0.043892 | missense | CADPS2 | GRCh38.p7 | 7:122416159 | GAGATGCCTGGTTCA[C/T]GGTCTCTATATGAAA | 93664 |
rs114579299 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122537322 | AACAAAAGATTATGC[C/T]CCAGAGAATACAGAA | 93664 |
rs114586543 | snp | G/T | 0.0644693 | 0.167566 | intron-variant | CADPS2 | GRCh38.p7 | 7:122492065 | TAGTCCCAGCAACTC[G/T]GGAGGCTGAGGTAGA | 93664 |
rs114587469 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122666754 | CATGTGGCAGCAACC[C/T]GTGGGCAGCTTTTCT | 93664 |
rs114588921 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122553456 | ATCCAAATCATGGTT[C/T]CATTTCTAAGAGCCC | 93664 |
rs114591536 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | CADPS2 | GRCh38.p7 | 7:122615729 | TGGTAAACATTGATA[A/C]CATCATACTAACTCA | 93664 |
rs114598019 | snp | A/C/T | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122770266 | ACCCACCCTATATCA[A/C/T]GCAAATCATGAAATC | 93664 |
rs114603534 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122777014 | AAATTAGCCAAGCAC[A/G]GCAGTGTGTGCCTGT | 93664 |
rs114611010 | snp | A/C | 0.030278 | 0.119257 | intron-variant | CADPS2 | GRCh38.p7 | 7:122742581 | ATAAGTGAGAGGGCC[A/C]CTTCCCACATTCTAA | 93664 |
rs114616735 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122760447 | TAGTAAGAGTCAACA[G/T]CAACAAAATTTTGGA | 93664 |
rs114618578 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | CADPS2 | GRCh38.p7 | 7:122668498 | AATAACTGGATCCAC[A/G]GCAGGTTGGTGGTGT | 93664 |
rs114641382 | snp | A/G | 0.021333 | 0.101051 | intron-variant | CADPS2 | GRCh38.p7 | 7:122430366 | TTCAGGAAACAGTAG[A/G]AACTGTTATCAAATG | 93664 |
rs114651297 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | CADPS2 | GRCh38.p7 | 7:122464014 | TGGAAGCTATGATTT[C/T]TCCAGCAGAAATAAA | 93664 |
rs114659528 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122377891 | TTTCTTTGTGGTTGT[C/T]TTCCACTCTAAGACA | 93664 |
rs114663787 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | CADPS2 | GRCh38.p7 | 7:122609128 | TGGCACCAAGATCTA[C/T]CTTCACCTTCCATAG | 93664 |
rs114665440 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | CADPS2 | GRCh38.p7 | 7:122399286 | TGTGTATATATGTGC[A/G]TATCCTCCACTAGAT | 93664 |
rs114671856 | snp | C/G | 0.0263992 | 0.111815 | intron-variant | CADPS2 | GRCh38.p7 | 7:122503434 | TTTTTATCTTAGAAA[C/G]TAGTATCTACTGCAA | 93664 |
rs114709786 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122655913 | ACATATAAAGAGCTT[A/G]GAAGTCATCACTCCC | 93664 |
rs114715633 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122485279 | TGTCAAAAGCCAAGA[C/T]AGGCTGAAAGCGAGG | 93664 |
rs114724315 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CADPS2 | GRCh38.p7 | 7:122755894 | TCTTTGCGATGTAGA[C/T]GTTTTCCTGGATTCC | 93664 |
rs114727369 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CADPS2, LOC105375481 | GRCh38.p7 | 7:122528938 | CTTTTCTTTTTACAT[A/T]TTTGAAAAAGAAAAT | 93664 |
rs114732355 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122867659 | CATTCCCAGCAGTTG[C/T]AGCCCCCAGGATCAG | 93664 |
rs114735343 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122876356 | GAATCCAGCAAATCT[A/G]ATTTTATATTTATTT | 93664 |
rs114748152 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | CADPS2 | GRCh38.p7 | 7:122738042 | GTAGGCAGTGAATGC[A/G]TCTTTGAGCACATAG | 93664 |
rs114752619 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122769075 | GTGAGATACAGACCA[A/C]AAGAGTTTCAGAGAA | 93664 |
rs114775681 | snp | C/G | 0.0456336 | 0.143994 | intron-variant | CADPS2 | GRCh38.p7 | 7:122397299 | TTTGCTCAGAATTCA[C/G]CAAAGAGTTATTTTT | 93664 |
rs114776922 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | CADPS2 | GRCh38.p7 | 7:122424496 | GGTGAGCCATAAAAT[G/T]TCAGATACATGTGAG | 93664 |
rs114780392 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122365339 | CGACAGCACCTGTGG[A/G]ATTAACCAGCTGAGG | 93664 |
rs114824257 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122725993 | GAGTTGGTGTCTCCT[A/G]AACAGTTTGAATTTT | 93664 |
rs114832379 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | CADPS2 | GRCh38.p7 | 7:122871715 | AAATCCAATTAACAT[C/T]TTCAATCTCCATCTT | 93664 |
rs114833231 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122860218 | TCTAGATTGTAACCA[A/C]CAAGTACCTGACACA | 93664 |
rs114848581 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | CADPS2 | GRCh38.p7 | 7:122351922 | TTACATTTTATTATA[G/T]CAATGGGGAAAATCC | 93664 |
rs114861359 | snp | C/G | 0.0901694 | 0.192235 | intron-variant | CADPS2 | GRCh38.p7 | 7:122400046 | GTTACAAGAAACACA[C/G]TGGCATTTTAGAATA | 93664 |
rs114868652 | snp | A/C | 0.0356815 | 0.128715 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122544380 | TGTAAGACAAGAGTG[A/C]ACAGTATCTAACCTT | 93664 |
rs114879674 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122617019 | TAGAAATCGTAAGAG[C/T]ATTGCTTCATATTTC | 93664 |
rs114896718 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant, nc-transcript-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122530538 | AAAGATAAATTTTCT[A/G]TATTCTAAGTATTGT | 93664 |
rs114897451 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | CADPS2 | GRCh38.p7 | 7:122490884 | TTAAATATCAGGTGT[C/T]CAATACTCTTTCCAG | 93664 |
rs114899889 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122882326 | CACACACTGAAACAT[A/G]AAAATATAGGTATAT | 93664 |
rs114907371 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | CADPS2 | GRCh38.p7 | 7:122422625 | CTCTATCTTAGGTAA[C/T]TCATCAATGTTAGAT | 93664 |
rs114911548 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122551520 | AGAGAATACATGTTA[C/T]AATAGTTCACGCAAG | 93664 |
rs114927952 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CADPS2 | GRCh38.p7 | 7:122419030 | TCTGAATGAGTTGCT[C/T]CTTTCTCTGAGCTCC | 93664 |
rs114975985 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | CADPS2 | GRCh38.p7 | 7:122382643 | CATTAATGTTTCCAA[C/T]AATAAAAACCTATAA | 93664 |
rs114990384 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122556985 | TCTCCCTATCATATG[A/T]ATATCTAATTCCCTA | 93664 |
rs115007241 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122321417 | AAATGATCCTCACAT[C/G]TCAGCCTCCCAAAGT | 93664 |
rs115016938 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | CADPS2 | GRCh38.p7 | 7:122520317 | TAAAATGCTTGTCTT[C/T]ACATAGTACCCGGTT | 93664 |
rs115027570 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | CADPS2 | GRCh38.p7 | 7:122584738 | CCCCATAAATTTAGA[A/G]AGTGCTATTTTTACT | 93664 |
rs115034622 | snp | A/G/T | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122661739 | AAAATATGTTTTTTC[A/G/T]CTCAACTTGGATTCC | 93664 |
rs115068165 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | CADPS2 | GRCh38.p7 | 7:122364283 | GGCTGGGCATGGTGG[C/T]GTGTGCCTGTAGCTT | 93664 |
rs115072856 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122435218 | AAATTAAAAAGGCAA[C/T]GTACAGAATGGGAGA | 93664 |
rs115082674 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | CADPS2 | GRCh38.p7 | 7:122834631 | AAACAGCATACCAGG[A/G]GATTATATACGGCGC | 93664 |
rs115083718 | snp | C/T | 0.030278 | 0.119257 | intron-variant | CADPS2 | GRCh38.p7 | 7:122384468 | TTTATAAATGAGGTC[C/T]GCTGGCTCACCTGTA | 93664 |
rs115100874 | snp | C/T | 0.021333 | 0.101051 | intron-variant | CADPS2 | GRCh38.p7 | 7:122683141 | GGAAGTGGTTCTTGG[C/T]GGGATGAGAGTTGGA | 93664 |
rs115105299 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122549135 | AGCACAGTGGCTCAC[A/G]TCTGTATTTCCAGCA | 93664 |
rs115108373 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | CADPS2 | GRCh38.p7 | 7:122515763 | CATTGCACATGTATA[C/T]ATATGTAACTAACCT | 93664 |
rs115119177 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554390 | CTATAAAGCCGTCTA[C/T]GGGTATAAAAACATT | 93664 |
rs115128853 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | CADPS2 | GRCh38.p7 | 7:122462141 | AGCAAATACGAAGTA[C/T]AAAATAAGAAAGATA | 93664 |
rs115142039 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | CADPS2 | GRCh38.p7 | 7:122492952 | TTCTGTTTTTAAACA[C/T]AAAATGAAACTAAGG | 93664 |
rs115153675 | snp | A/G | 0.0667028 | 0.170006 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122538498 | TTTTAAAAAATTTTC[A/G]TAACATTTAAATAAA | 93664 |
rs115176024 | snp | A/C | 0.0168055 | 0.0901129 | intron-variant | CADPS2 | GRCh38.p7 | 7:122807165 | GGTGGCCTACCCCAG[A/C]GGTATGCCCCAACCC | 93664 |
rs115177945 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122777651 | TCTCATGATAGTGAG[C/T]GAGTTCTCATGAGAT | 93664 |
rs115181708 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | CADPS2 | GRCh38.p7 | 7:122867895 | CTGCAATCTCACATT[G/T]GAAGGAAGCTGGGGA | 93664 |
rs115204152 | snp | A/T | 0.0310518 | 0.120672 | intron-variant | CADPS2 | GRCh38.p7 | 7:122451581 | AAGTTCACTGTATAC[A/T]TATTAATTGTGTTTA | 93664 |
rs115222540 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | CADPS2 | GRCh38.p7 | 7:122403429 | GCCAAGACCTAGACT[C/T]ACCCTCAAAACTGAG | 93664 |
rs115230174 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | CADPS2 | GRCh38.p7 | 7:122467918 | TCATCCTGCATGAGT[A/G]GGTCTGTTTCTGTCC | 93664 |
rs115232646 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122544443 | ACTTAAAACGACAAC[A/G]ATTTATTATTTCTTA | 93664 |
rs115233970 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122638639 | CTCTGGGTAGCTCTC[C/T]GTATCAGTCTAGAGG | 93664 |
rs115238632 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122391104 | TTAAATATAAATGTT[G/T]CTTTTTATTAATGTT | 93664 |
rs115240945 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | CADPS2 | GRCh38.p7 | 7:122676213 | TGATTAGTCTGTTTA[C/T]GAGAAACACCTACAA | 93664 |
rs115285443 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | CADPS2 | GRCh38.p7 | 7:122375301 | CCTAATTTCAAAATC[C/T]ATTACAAAGCTAAAA | 93664 |
rs115292368 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122385002 | ACAAACGGATAAACC[C/T]AGTATGAATGGAAGA | 93664 |
rs115309478 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122387441 | AGCTTTTTGTTATAT[C/T]TAGAGTACCACATTT | 93664 |
rs115315974 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | CADPS2 | GRCh38.p7 | 7:122486145 | TAACCCAACATCCAT[C/T]CTGCAGCCCACAGAT | 93664 |
rs115352515 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122433307 | AACATTTCTAAAAAA[C/G]CCCTATCTTCTGTTA | 93664 |
rs115377196 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122670628 | TCAGCCTCTGGAGTA[C/T]CTGGGAGTACAGGCA | 93664 |
rs115391586 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122789750 | ACATAAAACTTTAAA[A/G]CTTGTTTACAGAAAC | 93664 |
rs115437532 | snp | A/T | 0.046775 | 0.145601 | intron-variant | CADPS2 | GRCh38.p7 | 7:122389899 | ACTTAAAGTAAAATT[A/T]AAAAAAAATAAATTG | 93664 |
rs115449776 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | CADPS2 | GRCh38.p7 | 7:122594048 | TAAAGTAACTATGTT[A/T]TATCATTCTAGGCTT | 93664 |
rs115452777 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122462756 | ATTAGTTATGATGAT[C/T]ATCACCAAATGATGA | 93664 |
rs115462528 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | CADPS2 | GRCh38.p7 | 7:122386167 | CCTTATATATGCGAA[C/T]ACAGAAGCCAAAAAT | 93664 |
rs115468165 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122867238 | ATCCATCTCCTCTAC[C/T]AGAATATAAGCTTCA | 93664 |
rs115489931 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | CADPS2 | GRCh38.p7 | 7:122674795 | ATGTGTTCAGCAAAA[C/T]GCTGAGAAAAGTACA | 93664 |
rs115490246 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122551574 | TATTAAAACAGAGAA[C/T]AGGTTTTTACTACTG | 93664 |
rs115500452 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122398830 | ATAGCACCCAGCCAA[C/G]AATCTGGCACATTAA | 93664 |
rs115501625 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | CADPS2 | GRCh38.p7 | 7:122392957 | ACCAAATTATTCCTG[C/T]CCCACAGATTATATA | 93664 |
rs115502060 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122825532 | AGAAAGATTGACCAA[A/C]AGTGGTTAATATGAT | 93664 |
rs115512496 | snp | G/T | 0.0283406 | 0.115616 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122557195 | AAATAGTTTTCAGGC[G/T]CCCAAATTGCACAAG | 93664 |
rs115521960 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122453798 | TGCTTGACAGAATGG[A/T]GCCAGGGGGTCAGGT | 93664 |
rs115527420 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | CADPS2 | GRCh38.p7 | 7:122460657 | CATGGCAAAAATGTC[A/G]GCAGAAACAATAGAA | 93664 |
rs115537252 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122777757 | GTTTGTTCCCCTTCC[A/G]CCCTGCTTGTAAGTT | 93664 |
rs115560814 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122840729 | GAGACTAGTCTGAGT[A/G]ACACAAGGAGATGCT | 93664 |
rs115564296 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | CADPS2 | GRCh38.p7 | 7:122791090 | TGTGGGCCATGCTGA[C/G]TACCAGAACAAAATA | 93664 |
rs115565881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122851436 | GCAGTTCAGCTATCA[A/G]TTATGCTTCCCACAG | 93664 |
rs115582096 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122346304 | GCATGGGTGGTTGAG[A/G]TTGCAGTGAGCTGTC | 93664 |
rs115584305 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122455540 | GTGCTAGAACACCAG[A/G]TGGCATATTGTTGAT | 93664 |
rs115586225 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | CADPS2 | GRCh38.p7 | 7:122351902 | AGTTATGTAGCATTA[A/G]TATGTTACATTTTAT | 93664 |
rs115605086 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122809903 | CAGAATTTCCAAAAT[C/T]TCAGTCATTCAAAGG | 93664 |
rs115622760 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | CADPS2 | GRCh38.p7 | 7:122732257 | AAAGAAATATATCTC[A/G]GGTTTCATACCAAGA | 93664 |
rs115627929 | snp | G/T | 0.021333 | 0.101051 | intron-variant | CADPS2 | GRCh38.p7 | 7:122728162 | TAAAATGACAAAAAT[G/T]TTTCATCAAAATATT | 93664 |
rs115640853 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | CADPS2 | GRCh38.p7 | 7:122777925 | GCTGCTATAACGATA[C/T]GCAAAAATGTGAACT | 93664 |
rs115660701 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | CADPS2 | GRCh38.p7 | 7:122503517 | ATTTTAAGGGACACA[C/T]TGGCAAAATAGTTTA | 93664 |
rs115661950 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | CADPS2 | GRCh38.p7 | 7:122527297 | GGCTCTTCAACCACC[G/T]CTGAAAATGGCTTCA | 93664 |
rs115666027 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | CADPS2 | GRCh38.p7 | 7:122567756 | GTTATAATATTACTT[C/G]ACTTAGCCTCTGATG | 93664 |
rs115692844 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | CADPS2 | GRCh38.p7 | 7:122852453 | GTGCAAAACAGGGAA[A/G]GAAAGTAGAAAGCTT | 93664 |
rs115694041 | snp | C/G | 0.0260105 | 0.111035 | intron-variant, utr-variant-5-prime | CADPS2 | GRCh38.p7 | 7:122885788 | CAGCTCCTGCCAGCC[C/G]AGGCGGGGAGGAGGA | 93664 |
rs115699109 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122755224 | TGTTGCATGTAAACA[C/T]TATCAAGTTATGCCA | 93664 |
rs115699379 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | CADPS2 | GRCh38.p7 | 7:122499759 | TGTATCCTTAAGTTA[C/T]AATTATTCAACACCA | 93664 |
rs115707928 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | CADPS2 | GRCh38.p7 | 7:122868785 | TTCAAAAGGACAGTA[A/G]TAAAGATGCTCGCTA | 93664 |
rs115723003 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122373656 | AATGTAAGGCTACAG[A/G]GATCATGAAGAATCA | 93664 |
rs115733214 | snp | A/C | 0.0418186 | 0.138422 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122542763 | ACATCAGTCTAGAAT[A/C]TCTCTGATCACTCCG | 93664 |
rs115740169 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122651637 | CATGAAGAATTTGAG[G/T]GGGAGGAGGGATAAG | 93664 |
rs115746709 | snp | A/G | 0.200492 | 0.245049 | intron-variant | CADPS2 | GRCh38.p7 | 7:122645393 | TATGTACATGTGTGT[A/G]TATATATGTACATAT | 93664 |
rs115748678 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | CADPS2 | GRCh38.p7 | 7:122674790 | CCAGCATGTGTTCAG[C/T]AAAACGCTGAGAAAA | 93664 |
rs115749457 | snp | G/T | 0.0626037 | 0.165477 | intron-variant | CADPS2 | GRCh38.p7 | 7:122395372 | CCCAGCTCAGCTATA[G/T]GCTAAAACATTTCCC | 93664 |
rs115750655 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122879842 | AAAGTAAAAGGCTCC[A/C]AAATGCAAACCAACA | 93664 |
rs115773408 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122680146 | GGCACACAAAAAAAG[G/T]ACAATATCTGACCTC | 93664 |
rs115783573 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122647741 | ACAGCCTTTTCAAAA[C/T]GCTTTAAAAAAAGCT | 93664 |
rs115783715 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122412475 | AGATACTGATATTTA[G/T]GGGAATGCACATATG | 93664 |
rs115783806 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122437899 | CCGAAGGAAGTTCTA[C/T]GAGTTTATTTCAGCC | 93664 |
rs115784847 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | CADPS2 | GRCh38.p7 | 7:122465257 | ATCTACCATTTCCCA[A/G]AAAATCATAACTTGC | 93664 |
rs115791001 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122386076 | GAGAAACATTTCCCT[C/T]GTCATTATTTAAGGT | 93664 |
rs115792787 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | CADPS2 | GRCh38.p7 | 7:122395422 | TCATATTTAATGATA[A/G]GTGTCTTATTTAGGA | 93664 |
rs115811225 | snp | C/T | 0.298144 | 0.245321 | intron-variant | CADPS2 | GRCh38.p7 | 7:122645302 | GTACATATATACACA[C/T]ATGTACATGTGTGTA | 93664 |
rs115826207 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122869781 | TAATTTGCTAACTGA[C/T]ACAAACAGTAAAAGA | 93664 |
rs115849902 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122485336 | GAATGCAAAGGAAAA[A/G]TTGTTGCAGTAAATT | 93664 |
rs115852854 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122340792 | TATATTGGGATCAGG[C/T]TGAAGATGGTTTTGA | 93664 |
rs115860647 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | CADPS2 | GRCh38.p7 | 7:122485407 | AAAACAGCCTTATTG[C/T]TGATATGAAGAAAGT | 93664 |
rs115871712 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122609707 | AATTGCTGGCAGGAA[A/G]TCAGAACTACAGGAA | 93664 |
rs115878668 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122745384 | CCTCGCATCTAGTAA[C/G]AGACAGGGATAGAAT | 93664 |
rs115883651 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122769107 | CAAGTAAGTGAGTAA[G/T]ACAACTGTAAGTAAT | 93664 |
rs115900415 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | CADPS2 | GRCh38.p7 | 7:122411693 | TTGATAATCCTAAAG[G/T]TTCTGGAGACAATCC | 93664 |
rs115900423 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | CADPS2 | GRCh38.p7 | 7:122367602 | CAGGCTGGAGTGCAA[C/T]GGCGTGATCTCAGTT | 93664 |
rs115909133 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | CADPS2 | GRCh38.p7 | 7:122494329 | AAATGGAGAAGTACT[C/T]AAAGATGTATATGCA | 93664 |
rs115915124 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | CADPS2 | GRCh38.p7 | 7:122417645 | GACAACCTACTTAAT[C/T]TGGGGGCCGCTCTAG | 93664 |
rs115922847 | snp | A/C | 0.0337553 | 0.125452 | intron-variant | CADPS2 | GRCh38.p7 | 7:122595989 | ACTGCGGTCCACTGT[A/C]CAGAAGTGACATGTC | 93664 |
rs115925582 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | CADPS2 | GRCh38.p7 | 7:122692742 | GGGAGTGGGTGGATG[C/G]ACAGATAGCTGAAAG | 93664 |
rs115956637 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122815075 | TATGCCAATGCCAAG[A/G]AGGAGTTAAGATCTA | 93664 |
rs115963330 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122490018 | ACTGAATACATTTGC[C/G]TCAATTTTATATCTT | 93664 |
rs115966221 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | CADPS2 | GRCh38.p7 | 7:122496829 | TTCAGTGATTATTCA[C/T]GTCCATTAGGTCAAA | 93664 |
rs115988943 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122551480 | ATTTTTTAGGGGCCA[C/T]AGATAAGTGATAAAT | 93664 |
rs116004220 | snp | C/T | 0.021333 | 0.101051 | intron-variant | CADPS2 | GRCh38.p7 | 7:122726589 | AACTATTGAGTAAAT[C/T]TGACAGAGGATTAGC | 93664 |
rs116019460 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122345933 | CTTTTTTTTTTTTTT[G/T]TTAAATGGCTATCTT | 93664 |
rs116041457 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | CADPS2 | GRCh38.p7 | 7:122399179 | TACTTTTTTGGGCAA[C/T]ACATCCAAATTTAAA | 93664 |
rs116051239 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122531742 | ATGTTTTAAAAAATA[C/T]TGTTAGCAGGCTGGG | 93664 |
rs116062658 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122814358 | TTTTGATACATCAAA[A/T]GGATTACTCAGAGAA | 93664 |
rs116063204 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122771146 | TTCAAAGCTCCCCAG[A/G]GAAACATAACCTGCA | 93664 |
rs116069626 | snp | C/T | 0.030278 | 0.119257 | intron-variant | CADPS2 | GRCh38.p7 | 7:122521826 | TCACATTTTATAGAA[C/T]TGTCCCTCTTCCTTT | 93664 |
rs116072440 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122825794 | ATGTTTTGCAATACT[A/G]CAGTATAATATTACA | 93664 |
rs116084767 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122420170 | ATTCTTTTTCATTTT[C/T]AACTTTCTGAATAAA | 93664 |
rs116094325 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122379247 | TCTGAAAATTCTAAT[A/T]TTTTCCTGCCCTAAT | 93664 |
rs116099484 | snp | C/T | 0.0640965 | 0.167152 | intron-variant | CADPS2 | GRCh38.p7 | 7:122481382 | AAGTAAATTCAGTTC[C/T]CATAGCCTGATCAAT | 93664 |
rs116104910 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122526694 | TTCCCATTTATTACC[A/G]TCTTCTTAGCTCAAC | 93664 |
rs116105687 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | CADPS2 | GRCh38.p7 | 7:122400005 | ATGCCCATGGTTTTC[A/G]GAAGTTACAGGTGTT | 93664 |
rs116110592 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | CADPS2 | GRCh38.p7 | 7:122689401 | ATCAGTTAACAAAAG[G/T]AGGGCAACTCAGATG | 93664 |
rs116112166 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122610668 | AAAAATCATCTAATC[C/T]ACAATAGATGAATTT | 93664 |
rs116125947 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | CADPS2 | GRCh38.p7 | 7:122764271 | ACAGAAGAGCACACA[C/T]AGTAAATTTCCTGTC | 93664 |
rs116127842 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122794089 | CCTAGAGAATCTGAC[A/G]ATTACATGTCTTGTG | 93664 |
rs116129088 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122778383 | TAATAGAAAAGAAAA[A/C]GAAAAGAAAAACTGA | 93664 |
rs116129441 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | CADPS2 | GRCh38.p7 | 7:122728293 | TAAAATTTTAAAAGC[C/T]TGAAAAGGCTCTTAG | 93664 |
rs116130813 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | CADPS2 | GRCh38.p7 | 7:122826357 | TAAAACACAAAGTTT[A/G]AACAACATCCCAAGT | 93664 |
rs116132137 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122833444 | CAACCTTTGCCTCCC[A/G]GGTTCGAGCAATTCT | 93664 |
rs116140154 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | CADPS2 | GRCh38.p7 | 7:122421781 | AGCAGTATGTAAGAA[C/G]AGGGTTATTAGCTTG | 93664 |
rs116149105 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | CADPS2 | GRCh38.p7 | 7:122519781 | ATATTTAATATATGA[C/T]GTAGATGTGTAGAAT | 93664 |
rs116150966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122563227 | AAAGCATCACTATTC[C/T]TGATCTATTGCCCTC | 93664 |
rs116186767 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122735531 | TTCTGTTGAAATGTG[G/T]GCCTTTTTCTAAACT | 93664 |
rs116200855 | snp | A/C | 0.0626037 | 0.165477 | intron-variant | CADPS2 | GRCh38.p7 | 7:122395482 | TAGCACACTGAAAGA[A/C]GCTTTATTTATTCCT | 93664 |
rs116202316 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | CADPS2 | GRCh38.p7 | 7:122487970 | GAATACAAAACCATT[A/T]ATGAGATTGACGCTA | 93664 |
rs116212999 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122665537 | ATACACCTAACTTAC[C/T]TGAAACATGCTCAAA | 93664 |
rs116239319 | snp | A/C | 0.0629771 | 0.165899 | intron-variant | CADPS2 | GRCh38.p7 | 7:122386539 | AAACAAAATATAAAT[A/C]AAATAGAAAGAATAG | 93664 |
rs116286748 | snp | A/C | 0.0225045 | 0.103662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122867019 | ACAGGACTTTTTATT[A/C]TTGCTTTAGTGCTAT | 93664 |
rs116297252 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | CADPS2 | GRCh38.p7 | 7:122495349 | ACTTTTCTGTTTATT[A/T]TATTATTTCCATGAC | 93664 |
rs116297923 | snp | C/G | 0.0383715 | 0.133092 | intron-variant | CADPS2 | GRCh38.p7 | 7:122409707 | ATCTTGAGAATACAG[C/G]GTCTTGTCTACAACC | 93664 |
rs116300922 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | CADPS2 | GRCh38.p7 | 7:122446963 | TTTTTGGGGCCTTTT[A/T]AAATTGTTTTGGGTG | 93664 |
rs116314065 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | CADPS2 | GRCh38.p7 | 7:122726832 | TGAATGAGGTGGATA[A/G]CTAACTATAGGTGTT | 93664 |
rs116316482 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122832173 | ACATTTAAATAAATA[C/T]TGTAATCCCCTCAAA | 93664 |
rs116317352 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122787500 | ATTCAACTTCAAAGG[G/T]AAGTTAGGAATGGTC | 93664 |
rs116325363 | snp | A/G | 0.040671 | 0.13668 | intron-variant | CADPS2 | GRCh38.p7 | 7:122468953 | ACTGATTCAAATTTC[A/G]ATTCTAAAAGACTAC | 93664 |
rs116333853 | snp | A/T | 0.0298908 | 0.118541 | intron-variant | CADPS2 | GRCh38.p7 | 7:122390385 | GTACAGCTTGGTAGA[A/T]TAGAGGAACTGAGTT | 93664 |
rs116340816 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | CADPS2 | GRCh38.p7 | 7:122665270 | CATGCTCAACCACCT[A/G]ACCCCAAGCCTTTTC | 93664 |
rs116359524 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | CADPS2 | GRCh38.p7 | 7:122371243 | TGGCTTCAGGGCTGT[A/G]TTAGTCTGTTCACAC | 93664 |
rs116384589 | snp | G/T | 0.0562307 | 0.157967 | intron-variant | CADPS2 | GRCh38.p7 | 7:122408467 | CCTCACTCTGTCACT[G/T]GGGCTGGAGTGCAGT | 93664 |
rs116401775 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | CADPS2 | GRCh38.p7 | 7:122674208 | TCCCCGCCCGCACCT[C/G]TCCCTTCACACCTCC | 93664 |
rs116408877 | snp | A/C | 0.0402882 | 0.136092 | intron-variant | CADPS2 | GRCh38.p7 | 7:122495408 | AATCGATAAACATCA[A/C]GTACTTTTTGCATGT | 93664 |
rs116429110 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122628958 | ACATTAAAACTCTTC[C/T]AGATCTGGCAGTTTG | 93664 |
rs116437842 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122772647 | ACTAAAATACAAAAA[A/C]AAGGGCTCAAAGATT | 93664 |
rs116441223 | snp | A/G | 0.0170251 | 0.090679 | upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122887450 | GACACTCAGTCGCTG[A/G]TGGTTCTGGCCTCAA | 93664 |
rs116461121 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122555117 | CACAAATATGCCTCA[C/T]GTTTTAATATTATCA | 93664 |
rs116467718 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122759417 | AAGACTGTTTGAATA[A/C]AGTTATGTTTCTTTT | 93664 |
rs116482591 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | CADPS2 | GRCh38.p7 | 7:122362688 | ACAAGGTTTTTTCAA[C/T]AGGAAAAGGGAAATT | 93664 |
rs116514375 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122440486 | TTACAACAATCACAT[A/T]TCTATCACACAATCC | 93664 |
rs116516739 | snp | G/T | 0.0368353 | 0.130617 | intron-variant | CADPS2 | GRCh38.p7 | 7:122398204 | GGCTTTTAGTAGTAA[G/T]ATTTCAACAGAGAAT | 93664 |
rs116529348 | snp | C/T | 0.040671 | 0.13668 | intron-variant | CADPS2 | GRCh38.p7 | 7:122434664 | ATCATAACAGGCACA[C/T]GTAGTTAAATGAATA | 93664 |
rs116550774 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122480308 | TATAATTTTTTTTTT[A/T]TTTTTCCTAGTTATT | 93664 |
rs116558902 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | CADPS2 | GRCh38.p7 | 7:122752273 | TACTCTATAAAGATA[C/T]CTACTTACATTTTAA | 93664 |
rs116575846 | snp | C/G | 0.0263992 | 0.111815 | intron-variant | CADPS2 | GRCh38.p7 | 7:122416666 | AAAACAACTCTGACA[C/G]CTAGCAATTGACTGA | 93664 |
rs116579485 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122513774 | TGGGTGACCCCAAAA[A/T]GTGCCTGCACCAATC | 93664 |
rs116583857 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CADPS2 | GRCh38.p7 | 7:122466067 | AAACTTTGTCCTATA[C/T]CTAACTATTGACGAG | 93664 |
rs116603429 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122362487 | TTCTAAAACTTTATA[C/T]TTCTATGAAATAAAA | 93664 |
rs116610094 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | CADPS2 | GRCh38.p7 | 7:122400380 | AGGCGGAGGTTGTGG[C/T]CAGCCAAGATCACTC | 93664 |
rs116620769 | snp | A/C | 0.0887219 | 0.191022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122673974 | GTCCCCAACCCTGAG[A/C]GGGGAGGCGGCTGAG | 93664 |
rs116631137 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | CADPS2 | GRCh38.p7 | 7:122382774 | GTGAGCTATGAATAT[A/G]CCACTGCACTTCAGC | 93664 |
rs116641208 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | CADPS2 | GRCh38.p7 | 7:122522882 | CTCCAGTTTCACCCA[C/T]GTGGCTGCAAACGAC | 93664 |
rs116647777 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | CADPS2 | GRCh38.p7 | 7:122661057 | GGAGTGGCTGTATTA[C/G]CTTAAGACAATGTAG | 93664 |
rs116650767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122792938 | CCAACTACATATTTG[C/T]ACAAATTAAAGCATT | 93664 |
rs116653053 | snp | C/T | 0.021333 | 0.101051 | intron-variant | CADPS2 | GRCh38.p7 | 7:122710773 | CATTATTTTTGTACC[C/T]ATTTGGCAGTCATTT | 93664 |
rs116653585 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122810624 | AAGCAATATAACCAT[G/T]TATTCGCAGGATTTT | 93664 |
rs116675296 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | CADPS2 | GRCh38.p7 | 7:122515767 | GCACATGTATATATA[C/T]GTAACTAACCTGCAC | 93664 |
rs116686079 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | CADPS2 | GRCh38.p7 | 7:122744814 | ATTGATCTCCCAGTC[C/T]GATTCAAACCTCAGC | 93664 |
rs116686323 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122803927 | TACTTAGGATCCCTA[A/C/G]TTTTGACCTGCTGCT | 93664 |
rs116702506 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | CADPS2 | GRCh38.p7 | 7:122499892 | AAGAATCTTAAAAAC[C/G]TGACTAAAAAAAGTC | 93664 |
rs116727888 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122345060 | CCCCGCCATCCCCCC[A/G]GCCCACACACCAACA | 93664 |
rs116737929 | snp | A/G | 0.02016 | 0.0983543 | intron-variant, upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122622827 | ATCATTCAAAATCTA[A/G]CCTAAGAAATCTGCA | 93664 |
rs116769037 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122605460 | TGTATGACTATTTTA[C/T]AGCAATATGATCCCA | 93664 |
rs116773323 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122559826 | AGATAACCCGAGAAC[A/C]CTCTGGGCACCACCT | 93664 |
rs116810629 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | CADPS2 | GRCh38.p7 | 7:122491792 | CTTTTAATATGCTAA[C/T]GTAGGCTATAAATCT | 93664 |
rs116811116 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122851510 | ACCAGTACTAAAAAT[A/G]ATAGCTAAGACTTAA | 93664 |
rs116819557 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122431714 | AAAGTATTGTCTTAA[G/T]AAGTAAATTGAGTTG | 93664 |
rs116846098 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | CADPS2 | GRCh38.p7 | 7:122359869 | ACTCATTTATAACTA[C/T]AGCAGCAATAAAGCC | 93664 |
rs116882368 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122809940 | TGGCAGGTGCTAATG[A/G]TTATTACACACATAT | 93664 |
rs116907810 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122707503 | TGCACTGCTCAGATA[A/G]CATCTTTAAGATGAA | 93664 |
rs116908038 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant, upstream-variant-2KB | CADPS2, LOC105375481 | GRCh38.p7 | 7:122528483 | TAGACTACTACAAAA[A/C]TTATAACGTTCAGCT | 93664 |
rs116924866 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122371388 | CAAAGGAAAAGCAGG[C/T]ATCTTCTTCACAGGG | 93664 |
rs116930112 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122513370 | ATAATGTTGTGCTTC[C/G]ATGTAATCACATTTC | 93664 |
rs116952379 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122559259 | AACCAAACACTGTAA[C/T]AGCGGCACCCTAGAA | 93664 |
rs116959852 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122411617 | AGTGAGTCTGACTTT[C/G]AAATACATTTTGTGC | 93664 |
rs116961652 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122376042 | CAGTGAGATATTAGC[A/T]CACATCTGTTTGGAT | 93664 |
rs116979086 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | CADPS2 | GRCh38.p7 | 7:122720504 | TGTATATGTATATAC[A/G]TATAAGTATATATAC | 93664 |
rs117009735 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122773390 | TCATTTACTTAATGC[C/T]ATTAATTACAGCACT | 93664 |
rs117023978 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122690618 | TCATCCTCGTAACTG[A/G]TTGGAGAAGGTCATC | 93664 |
rs117033822 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122484430 | TTCAACTCTTTGTGT[C/T]AGAACAACTGGACAT | 93664 |
rs117041621 | snp | A/C | 0.0729998 | 0.176553 | intron-variant | CADPS2 | GRCh38.p7 | 7:122632175 | GACCATATGGGTGCA[A/C]GTGTCCTTTTGATCA | 93664 |
rs117042526 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | CADPS2 | GRCh38.p7 | 7:122372694 | TCATCTACTTTATGT[C/T]GAGTTAATTATTATG | 93664 |
rs117049257 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant, nc-transcript-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122530938 | TTGATTGTGAATGGG[A/T]AAGTGTTCACATGTA | 93664 |
rs117053568 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122643819 | CCATGGACTTGGCAC[A/G]GTAGCTTATGCCTAT | 93664 |
rs117062013 | snp | A/C | 0.0356815 | 0.128715 | intron-variant | CADPS2 | GRCh38.p7 | 7:122638221 | AGACAAGACTATACC[A/C]TTTCTGGAAAGCCCT | 93664 |
rs117063956 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122417548 | GATCCATAGACATGA[A/G]TGATCAAATGTTTCA | 93664 |
rs117066703 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122373948 | AAGCCAGACAAAAGA[C/T]ACTGCCAGAAAAGAA | 93664 |
rs117070046 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122764211 | GATCCCTAAGGCTGA[A/G]GACCCTCTTACGTGT | 93664 |
rs117076838 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122342783 | TGAAGTTAACAAGAT[A/C]CATTTACTTACTTAT | 93664 |
rs117077444 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | CADPS2 | GRCh38.p7 | 7:122685087 | ACTACATGTGGAATA[A/G]CAATGTTATTGCTTT | 93664 |
rs117083436 | snp | A/C | 0.021333 | 0.101051 | intron-variant | CADPS2 | GRCh38.p7 | 7:122797371 | CAAAGGAATATAAAT[A/C]ATTCTATTAAAGACA | 93664 |
rs117084963 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122751821 | GTGTAACTCAGGCTA[C/T]GGTATATGCATTTTG | 93664 |
rs117085212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122359310 | ACTCATAATACTTAA[C/T]AGTAGGCTGCCATAT | 93664 |
rs117092802 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | CADPS2 | GRCh38.p7 | 7:122572867 | TATTCCCTTAGCACC[C/T]GGTGGAGGGTTGGCC | 93664 |
rs117103235 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122799947 | TTACAAGCTATGTGA[C/T]TGTTGAAAGCCTGCC | 93664 |
rs117107007 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | CADPS2 | GRCh38.p7 | 7:122565414 | CAGGAAGATAGTGGG[A/G]AATAAGGTCAGGACA | 93664 |
rs117113250 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | CADPS2 | GRCh38.p7 | 7:122716911 | ATAATGGGGTTTTGT[C/T]CCTACTTGCAATGTG | 93664 |
rs117115924 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122674868 | CCAAATAAAATATTG[C/T]CTCATAATTTCCATA | 93664 |
rs117117583 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | CADPS2 | GRCh38.p7 | 7:122846057 | GCTGTTTATCTGTAA[A/G]ATTTCACAGTTAAAA | 93664 |
rs117137149 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122374778 | ACCTAATGTAGGTGA[C/T]GAGCTGATGGGTGCA | 93664 |
rs117149846 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | CADPS2 | GRCh38.p7 | 7:122522718 | CTTCAGCCCCATCCT[C/T]CCCATCCCCCACCCC | 93664 |
rs117150554 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122607548 | AACAAATACTACTAA[C/T]CATAATTCTATAAAC | 93664 |
rs117152976 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122576850 | ATGAAACCTCTGCCT[C/T]CCGGGTTCAAGTGAT | 93664 |
rs117156132 | snp | C/T | 0.00716266 | 0.059414 | utr-variant-3-prime | CADPS2 | GRCh38.p7 | 7:122319811 | ATGTATCTCGCTTTA[C/T]ACAGAAAACATCATT | 93664 |
rs117158232 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122598557 | TTTAATTATGTAGTG[C/G]GTGGAAATTAGGGTG | 93664 |
rs117171360 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122809140 | TGTATAAATATTGTT[C/T]CATATAACAATGTTT | 93664 |
rs117189513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122468165 | CTTCACTTCAGTCAA[C/T]AACAAAAGGAAATCT | 93664 |
rs117191341 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | CADPS2 | GRCh38.p7 | 7:122333965 | AGATGAATACCAGAG[C/G]CAGATTCACTGTTGA | 93664 |
rs117198955 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122694514 | GGACACAGTAACTTG[A/G]AGGTCTGATAAAGAT | 93664 |
rs117201315 | snp | A/T | 0.0337553 | 0.125452 | intron-variant | CADPS2 | GRCh38.p7 | 7:122683619 | CATAGTGAAATAAAT[A/T]TTAAAATCACTGCTA | 93664 |
rs117209148 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122355969 | GATTTACAGAAACAC[C/T]GTGGAAATATTAGTT | 93664 |
rs117212957 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122332795 | GTTCACTACTACTTT[C/T]AAAATACCCTTCATT | 93664 |
rs117213985 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | CADPS2 | GRCh38.p7 | 7:122650636 | ACATTTTAGCAGAAA[A/C]CTTATTTTAGAATAT | 93664 |
rs117219396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122353849 | TCAGTTCTGCTCCCA[C/T]TTGTTTTTAGTCATT | 93664 |
rs117224926 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | CADPS2 | GRCh38.p7 | 7:122348160 | GCCACTGCTTAGACA[C/T]TCAGTTCAGTCAGTC | 93664 |
rs117231375 | snp | C/T | 0.229723 | 0.249176 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122541772 | ATATATTTATATATT[C/T]ACATATATTCATATA | 93664 |
rs117244296 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | CADPS2 | GRCh38.p7 | 7:122579169 | TTCCAACCTATTGAG[A/G]TCATTAGTATAGATT | 93664 |
rs117245957 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | CADPS2 | GRCh38.p7 | 7:122685404 | AGCCCATTCTTCAAG[C/T]GTTTGATGGCAGCTA | 93664 |
rs117251349 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122384604 | GCGAAGTATAAAATT[A/C]TTTTGCAATGAAATT | 93664 |
rs117258271 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | CADPS2 | GRCh38.p7 | 7:122322121 | TTTGTGTTTATTCCT[A/G]TAACTCTCTTGTAAT | 93664 |
rs117272728 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | CADPS2 | GRCh38.p7 | 7:122594757 | TAATTTTAAAGAGAA[C/T]AAATTGGTCACATCT | 93664 |
rs117316961 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122773881 | CTAGTTTTGTTCCCT[A/G]ATGTTTGGCATTCAC | 93664 |
rs117323238 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122637966 | ATTTGGGCTGTAATC[C/T]AGTAGGTGCTCCTTA | 93664 |
rs117330987 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122637541 | TTTAAAATAGCTATT[C/T]TGTCTTTTAGCTCTT | 93664 |
rs117345509 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122372825 | CAGATTTCCCAGAGA[C/T]GTAGAATCAGTTAAG | 93664 |
rs117349510 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122589601 | AAGATAAGTAAGTTT[C/T]CATGGGAACATGGGT | 93664 |
rs117352546 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | CADPS2 | GRCh38.p7 | 7:122729559 | TTTTAATAATAGCCA[C/T]TCTAACTGAGGTGGG | 93664 |
rs117352662 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122517500 | TCCAAACTGGCTATA[A/C]CATTTTGAGTTACCA | 93664 |
rs117356741 | snp | C/G | 0.0232847 | 0.105357 | intron-variant, nc-transcript-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122530931 | TGCTGGATTGATTGT[C/G]AATGGGAAAGTGTTC | 93664 |
rs117399586 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122802060 | CTATTTAGAAAAGCT[A/G]TAAGATGTCTAAACA | 93664 |
rs117411397 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122328683 | CCTGTAAGGGCATGC[A/G]TTACTCACTGCATTT | 93664 |
rs117416410 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122408141 | GTGATTTCACTTTTA[A/C]TATAATAGCATAATC | 93664 |
rs117448502 | snp | C/T | 0.0279526 | 0.114869 | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122704717 | CCCTCTCTTCTGCCC[C/T]CGTCTTACAACAAAA | 93664 |
rs117459936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122516548 | GTCTCTTAGAGTAAA[C/T]ACATGAAGAAGGAAT | 93664 |
rs117461597 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122481232 | GTGCAGTGGTGCGAA[C/T]GTGGCTCACTGCAAG | 93664 |
rs117461769 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | CADPS2 | GRCh38.p7 | 7:122732296 | ATTAAAGTAAACCGA[A/G]TATCTGAAGGTACAA | 93664 |
rs117462388 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | CADPS2 | GRCh38.p7 | 7:122524002 | TTCCAAAGAAAAGGA[C/T]ATTTTGCATCTCTTG | 93664 |
rs117467796 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122362911 | CCATCACATCATTTG[C/T]GACATGATGTAAGAA | 93664 |
rs117481878 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122632449 | CTTTGATTTGCATTT[C/T]TCTGATGATTAGTGA | 93664 |
rs117491394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122479530 | AAGCAAAGGAGTTTG[C/T]TCACACCTTTATTAT | 93664 |
rs117499731 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122841797 | AGACCATCAGCCTGA[A/G]TCAATACAATAAAAG | 93664 |
rs117509985 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | CADPS2 | GRCh38.p7 | 7:122335450 | GATGGAGTTTCACCA[C/T]GTTGAAAGTTCACAT | 93664 |
rs117525447 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | CADPS2 | GRCh38.p7 | 7:122411213 | TATTAAAACCTGAGG[C/T]CTTTGATTACTTTTT | 93664 |
rs117526743 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | CADPS2 | GRCh38.p7 | 7:122349234 | GATTCAGATTAGTTT[C/T]TATTAAGAATATTGT | 93664 |
rs117541457 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122737952 | ACATACATCAATACC[C/T]GAGTTTAGATAATTG | 93664 |
rs117549095 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122640055 | TCAATTTTCAGCTCC[A/G]TACCCCGATCATTCA | 93664 |
rs117558133 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122546838 | CATCATTAAAACACT[A/G]GTTCCTTGTATATTT | 93664 |
rs117566556 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122619129 | TTTCACTTAAACATT[A/G]ACTCAGCAGCCTAAT | 93664 |
rs117580384 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122372106 | ACTATTATATTACTC[A/C]TACTTTATAGGAGAG | 93664 |
rs117586214 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | CADPS2 | GRCh38.p7 | 7:122868842 | ACTGATAATTTCAAC[A/G]AAGAGATAGAACATA | 93664 |
rs117586487 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-5-prime | CADPS2, RNF148 | GRCh38.p7 | 7:122702945 | TCATAATGAAACAAA[A/G]TAACAAGACTTGTGA | 93664 |
rs117596663 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | CADPS2 | GRCh38.p7 | 7:122470825 | TTTTAAGGCCAGAGA[C/T]AGACAACTGTGGAGG | 93664 |
rs117603384 | snp | A/G | 0.021333 | 0.101051 | intron-variant | CADPS2 | GRCh38.p7 | 7:122829012 | GGACCTCATGTGTGC[A/G]AATGTTTTAAATCAT | 93664 |
rs117604248 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CADPS2 | GRCh38.p7 | 7:122669413 | GAAATCTCCAGAGAT[A/G]AACAGGAGGATTATA | 93664 |
rs117612827 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122418620 | CAGTGAACTATGGAA[A/G]GATGATAGTAGGAAT | 93664 |
rs117613610 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122786797 | CAGACTTATTTGGTC[A/G]TGCTTTGTTCAAAAG | 93664 |
rs117618224 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122696540 | ATAGCTAACTACTGC[C/T]CTTCTACCTGTGTCT | 93664 |
rs117637060 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | CADPS2 | GRCh38.p7 | 7:122824005 | TTACACATGCAAAAG[A/T]CATTGGCTTGTACTT | 93664 |
rs117657596 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122553044 | CTGGAATGCCAGTTC[C/T]CCCACTGTCTACCTG | 93664 |
rs117660016 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122363035 | GCCTAGGGAAAAAAA[A/G]TCCACCCACAAAATT | 93664 |
rs117664793 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122844434 | AGGAGATGAATCACC[C/T]AAACGACATATCTTT | 93664 |
rs117673523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122540329 | TAATTTAAAAGGAAT[A/G]CTAAGTTTTAAAATA | 93664 |
rs117678283 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122815442 | ACCTCAGAAAAGTTC[A/G]TCCACAATTTGTAAC | 93664 |
rs117691391 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122538999 | ATGTTTAATGAAAAA[A/T]ATTAAATATCTATAG | 93664 |
rs117695732 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122562103 | GTCTCTCAAAATCTA[C/T]GAAACTTTCATCCTT | 93664 |
rs117703576 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122860594 | CCCCCAAGGATAAAG[A/G/T]ACATTAAAACATTTA | 93664 |
rs117710969 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | CADPS2 | GRCh38.p7 | 7:122357132 | ACACTGATATTTCCA[A/C]CTCTAATCCATTACA | 93664 |
rs117720180 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122371853 | GATCAGTACTGCCAA[C/T]GGAGACAGCAAATGC | 93664 |
rs117728490 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122483909 | TGACAAAAGATGTGC[G/T]AGATCTGTTCACTGA | 93664 |
rs117741997 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122343576 | AACTGATGGCAAGAA[A/C/T]GGATTGCAGTAAATA | 93664 |
rs117742715 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | CADPS2 | GRCh38.p7 | 7:122773587 | CCAGACCAGAAGTTC[A/T]AAAAAGGCTTCCTAA | 93664 |
rs117748200 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122486817 | AAGAAATTGCCACAT[C/T]CACACCAACCTTCAA | 93664 |
rs117757538 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | CADPS2 | GRCh38.p7 | 7:122321718 | CTCCTGAACTCAGGT[A/G]ATCCGCCCACCCCAG | 93664 |
rs117763610 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122603397 | CCTGTAAATTTCCTG[G/T]ACTTAAAAATAGGAT | 93664 |
rs117771884 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122468047 | AACACTCAGAGTGCT[A/T]TTCAGAGATGTATCT | 93664 |
rs117772415 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122463734 | AAACAGTATTTTGAC[C/T]GGAAACTGAAAGGTT | 93664 |
rs117777423 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | CADPS2 | GRCh38.p7 | 7:122587978 | AGTGATGCTGAGCTT[G/T]TCTCATGTTTGTTGG | 93664 |
rs117784025 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122798498 | AATGTATATAGATGT[C/G]CTATATTATCCCAAA | 93664 |
rs117794979 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | CADPS2 | GRCh38.p7 | 7:122828281 | GGTATAATTATTCTC[C/T]TCTACTTTCAACTTA | 93664 |
rs117811799 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | CADPS2 | GRCh38.p7 | 7:122674175 | CGCTGTCCTGCAAGC[A/G]CCCCGCACAGCCCCG | 93664 |
rs117830557 | snp | C/T | 0.0256215 | 0.110247 | intron-variant, utr-variant-5-prime | CADPS2, RNF148 | GRCh38.p7 | 7:122702831 | AAAGAAGATAGCTTG[C/T]TGGCGGCAGATTACT | 93664 |
rs117841543 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122615023 | ACATCATTATCTAGA[A/C]AGGGACACACTAGTT | 93664 |
rs117885400 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | CADPS2 | GRCh38.p7 | 7:122619226 | ACAATAGAGAAAAGA[C/T]AAAATGTTCTGAACT | 93664 |
rs117891231 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | CADPS2 | GRCh38.p7 | 7:122325773 | AGAAAATCTGTTAAG[C/T]TGACCTAGGCTGTTC | 93664 |
rs117898682 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122766146 | GGAACACCACACTCT[C/T]GCAGTAACCCAGTTC | 93664 |
rs117898692 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122378099 | CTTAATACTATATTA[C/T]GAAACTCTTCATTTA | 93664 |
rs117913846 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122560008 | GCTGCACATTGTTGG[A/G]TCTGAAAGGCTATTG | 93664 |
rs117930215 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | CADPS2 | GRCh38.p7 | 7:122514391 | TTAGACTTTCACAAC[A/T]TTTAAAACTAAAATC | 93664 |
rs117961527 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122496610 | ATTTTTCATTTTTAT[C/G]ATTTGTTTTTTATGT | 93664 |
rs117973196 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122367943 | TCAAAGCTGGCAACA[C/T]AGCATCTCTCTAACC | 93664 |
rs117989618 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122413665 | GAACATCCAGCAAAA[C/T]AAGTATCAGTGCAGA | 93664 |
rs117989706 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122371533 | GCCAATTACCTCCAC[C/G]TGCTCCCACCCTTGA | 93664 |
rs117994153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122550321 | ATTCAACAAAATGTG[C/T]AAATAGCCAAGCATG | 93664 |
rs117994344 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122401845 | GGAGTCAGTGAGTGA[A/G]TCTGTGAGGGGTGGG | 93664 |
rs117998729 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122813990 | AAAAATTACTTCGTC[A/G]ATGTGTATACAAGGA | 93664 |
rs118003563 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122805449 | AGGAGTGAGCCACCA[C/T]ACCCGGTCTTCAATT | 93664 |
rs118005173 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | CADPS2 | GRCh38.p7 | 7:122320660 | ATAAAATATGTACCT[A/G]TGTAAGTTTTTAATA | 93664 |
rs118007213 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122597040 | AGTGAATGCCAGGCT[A/C]ATTTTAACAACCAGC | 93664 |
rs118053525 | snp | C/G/T | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122603437 | AGAGATTTAAAGAAA[C/G/T]TAGAGAAATGAATAC | 93664 |
rs118057702 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122638640 | TCTGGGTAGCTCTCT[G/T]TATCAGTCTAGAGGC | 93664 |
rs118062639 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122322509 | TTTGGTTGGCTCTTG[C/G]TTAAGACAAGTGCCT | 93664 |
rs118066183 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | CADPS2 | GRCh38.p7 | 7:122334130 | TCTAATTTTATTTTA[A/G]GTGATGAATGAAATA | 93664 |
rs118066697 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122704048 | TTTCTATCATGTATA[C/G]GTTATCTTCTATGTG | 93664 |
rs118080968 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122385507 | GAGTTTGATTCCCAA[C/T]TGTCAACTGTAAGAC | 93664 |
rs118081769 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122555081 | ACATGCTTAAAAACC[A/C]AAGTCAATTATTTGA | 93664 |
rs118084179 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | CADPS2 | GRCh38.p7 | 7:122615007 | CAAAATTCCAATTAT[A/G]ACATCATTATCTAGA | 93664 |
rs118089846 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122500041 | TATAGCTACCGCTGT[A/G]TAAAGTACTCCAGAC | 93664 |
rs118090210 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122557420 | AGGATTTCATTATTG[C/T]AATTGGACAATTACT | 93664 |
rs118095105 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122880068 | TTTGGAAAACCTGTA[C/T]GCATTACTACTACAT | 93664 |
rs118097194 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | CADPS2 | GRCh38.p7 | 7:122496418 | TCCACCTGCCTTGGC[C/T]TCCCAAAATGCTGGG | 93664 |
rs118111263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122695361 | ATTATGACAAGATAT[A/G]TTTGCATCACTAGGT | 93664 |
rs118113605 | snp | C/G | 0.00226744 | 0.0335943 | missense | CADPS2 | GRCh38.p7 | 7:122438422 | TGACCACTTTCTTCA[C/G]CTCTTCTGCTGGTAT | 93664 |
rs118114013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122396633 | ATTTCCTGTGATACA[A/G]TCATAATGACTTTCA | 93664 |
rs118123338 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122327042 | CCTGTATCTAATTTT[C/G]CTCCTTCCTAATGAG | 93664 |
rs118125421 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122378447 | AGAGAAAATAGTATA[C/T]TATTGTAGCTTACTT | 93664 |
rs118145553 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122494830 | TCAAATTTACTTTTT[C/T]CCTTGCATATGTCTA | 93664 |
rs118154912 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122756672 | GAGAGGTGGCAGTGG[A/G]TGCATCACCTGAGGT | 93664 |
rs118161134 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | CADPS2 | GRCh38.p7 | 7:122851272 | GCAGTCCCCAGGGAT[A/G]TTCAACTGGGCCACT | 93664 |
rs118180169 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | CADPS2 | GRCh38.p7 | 7:122620824 | ATCTGAAAGGAATTC[C/T]CAAATTACAAAGAAT | 93664 |
rs118181380 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122576539 | ATGTTAGTGTGCATA[C/T]ATTAATGTACATTCT | 93664 |
rs118186770 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122683482 | TTCTGTATCAATATC[A/G]CTTTTAAAAATACTT | 93664 |
rs137870973 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122405949 | TTTCCTTCTTTTATA[C/G]ATATAGCACCTAGAG | 93664 |
rs137872208 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122464352 | GCACATGAATCTATA[C/T]GGATATAAACAAATG | 93664 |
rs137879621 | in-del | -/AAT | 0.455383 | 0.142541 | intron-variant | CADPS2 | GRCh38.p7 | 7:122515836 | AAAAATTAATTAAAA[-/AAT]AATAATAATTATATG | 93664 |
rs137897326 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122677592 | AGGGACTTCATGTAT[A/T]TTAACCCTCACAACT | 93664 |
rs137904021 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | CADPS2 | GRCh38.p7 | 7:122410960 | AGAGATTAAATAACT[A/T]GCCCAAAGTCATACA | 93664 |
rs137916835 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122606898 | GAAAGAGGGCAGCCA[C/T]AGGATGTATAATTTG | 93664 |
rs137917752 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122786770 | CATTTTTTTTTCTAT[A/G]AGAGTGGTTTTCAGA | 93664 |
rs137924027 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122777926 | CTGCTATAACGATAC[A/G]CAAAAATGTGAACTT | 93664 |
rs137924854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122709975 | TGACGAGTTAATGGG[C/T]GCAGCACACCAGCAT | 93664 |
rs137930197 | snp | C/T | 1.65192e-05 | 0.00287391 | intron-variant, synonymous-codon | CADPS2, RNF133 | GRCh38.p7 | 7:122698784 | ATTCCCAACATGAAA[C/T]GATATGTTCATATAA | 93664 |
rs137945584 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122459054 | GAAAATTTCCTATAA[A/G]TATGCCAACCAGAAA | 93664 |
rs137950690 | snp | A/G | 6.59533e-05 | 0.00574215 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698135 | CATTAGGCTTATAGC[A/G]TTCAAAGCAAATTAC | 93664 |
rs137959589 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122515392 | TTGCTCTCTTTCTGT[C/G]TTTCTCTGCAATTTC | 93664 |
rs137972115 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | CADPS2 | GRCh38.p7 | 7:122833038 | TGTGAGAAACAATCA[A/T]CTAGGGAGGAAAAAA | 93664 |
rs137983673 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122643111 | ATAATCAGCACAAAC[C/G]TAATGCTGATTCCAA | 93664 |
rs137989351 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | CADPS2 | GRCh38.p7 | 7:122368833 | CATGCAGATATGTGC[A/G]TAGGACTTTTGTTCT | 93664 |
rs137999417 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122744861 | ATGGCATTGTCTGGC[A/G]TGGGCAGGGAGCTGG | 93664 |
rs138006786 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122668808 | GTGGTGAAGAGGAGA[A/C]GCTCTCATCTCCTGA | 93664 |
rs138010713 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122764215 | CCTAAGGCTGAAGAC[C/G]CTCTTACGTGTTCCT | 93664 |
rs138013777 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122686096 | ATATCAGATCTTTAG[C/T]GAATATAATGGAATT | 93664 |
rs138019603 | snp | A/C/G | 0.02016 | 0.0983543 | intron-variant | CADPS2 | GRCh38.p7 | 7:122432551 | AAAGCTGAGGCAGGA[A/C/G]AACCACTTGAACTCG | 93664 |
rs138025711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122601517 | ACTTCACCACCACTG[C/T]GATTTCTCTGGTGGT | 93664 |
rs138030247 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | CADPS2 | GRCh38.p7 | 7:122566328 | GTAGGAATGTGCATT[A/T]ATATAGCCATTTCAG | 93664 |
rs138035841 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CADPS2 | GRCh38.p7 | 7:122845076 | AAGCCAAATAAATAA[C/T]CTACATTCTCTATCA | 93664 |
rs138056971 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | CADPS2 | GRCh38.p7 | 7:122878474 | TGAAACCCCGTCTCT[A/G]CTAAAAATACAAAAA | 93664 |
rs138059882 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122415963 | GTTAAATGTTCAGAT[A/G]TGTATCAAGACTATG | 93664 |
rs138071457 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122837572 | GAAGAATCAAATAGA[C/T]GCAATAAAAAATGAT | 93664 |
rs138083165 | snp | A/G | 0.000192741 | 0.00981495 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122697823 | CTTCCACTACTGAAT[A/G]AGGCTGGATGTCATT | 93664 |
rs138084674 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122377501 | GATGCCGATTATGCA[A/G]ACTTCTCACAAAAGG | 93664 |
rs138096320 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122470737 | CTGGCCTCAGGTGAT[C/T]CACCCTCCTTGGCCT | 93664 |
rs138105963 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122884907 | TACAGTTATAGTTGA[A/T]GTCAACTCAAAACCT | 93664 |
rs138107344 | in-del | -/TCT | 0.219648 | 0.248151 | intron-variant | CADPS2 | GRCh38.p7 | 7:122644379 | AGGTCAATCTCCAAA[-/TCT]TCTTGGAAGATGACA | 93664 |
rs138113305 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122809129 | TGTATATACATTGTA[C/T]AAATATTGTTTCATA | 93664 |
rs138119809 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | CADPS2 | GRCh38.p7 | 7:122674100 | ACTTCCCGGGGCCAG[C/T]GGTGCTGGCTGGCCG | 93664 |
rs138121685 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122722035 | TTGGTATCGATGGGA[C/G]ATATCTCAAAAGAAT | 93664 |
rs138122294 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122654258 | GTAAGTTATCCAGAA[A/G]ATCTAGCTAAGATCA | 93664 |
rs138127303 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | CADPS2 | GRCh38.p7 | 7:122396037 | CTAGTCTCGAACTCC[C/T]GACCTCAGGTGATCC | 93664 |
rs138129033 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122801065 | AACACTATTTGGGCT[-/A]AAGAGAAAATTAAAA | 93664 |
rs138140176 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, nc-transcript-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122530775 | TTAATTTTGAAGCAA[C/T]GGCTTCCAGCTACCA | 93664 |
rs138143182 | snp | G/T | 0.0130921 | 0.0798413 | utr-variant-3-prime, downstream-variant-500B | CADPS2 | GRCh38.p7 | 7:122319215 | TGTATGTGCCTATTA[G/T]GTACAAAGAACAGTC | 93664 |
rs138143545 | snp | A/C | 0.0441095 | 0.141807 | intron-variant | CADPS2 | GRCh38.p7 | 7:122382898 | TGGAAAGCAGTTTGA[A/C]GATTTCTCAAAGAAC | 93664 |
rs138143577 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122654062 | TGTCATAAGAAGAGA[C/T]GGGTCAAATGCTAGG | 93664 |
rs138147126 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | CADPS2 | GRCh38.p7 | 7:122617766 | AATCAACTATAAGCC[A/G]GGCACAGTGGCTCAC | 93664 |
rs138158664 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122775373 | CTTCATGTTCCCATG[A/G]GCTGTCTTTGCTGCC | 93664 |
rs138161043 | in-del | -/G | 0.0138799 | 0.0821421 | intron-variant | CADPS2 | GRCh38.p7 | 7:122347203 | ACTATTACCATTGCT[-/G]GAAAAAACAACTCAA | 93664 |
rs138166323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122803703 | GTAGTTTGTATGTCT[A/G]TGGGATCGGTGGTGA | 93664 |
rs138169066 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122522014 | CAAACTGCCCAGATA[A/G]GACCATAAAACCCCA | 93664 |
rs138174493 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122613825 | TTGAATTAATAATTC[C/T]GCTTGGATGCTTACT | 93664 |
rs138197674 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122491730 | TTTGGGATCATTAGC[C/T]TATTAAGAAGATAAA | 93664 |
rs138199185 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122428080 | TTTTTAGCTAGTGGA[C/T]TGATGGAGTGGAGCA | 93664 |
rs138204724 | in-del | -/GT | 0.0715223 | 0.175059 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122550059 | ATGTCTGAATATTTA[-/GT]GTGTGAATGCAGTTT | 93664 |
rs138205196 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122583441 | TTTATATTTATCACT[A/C]CCTTGAATTTCTTCT | 93664 |
rs138216060 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | CADPS2, LOC105375481 | GRCh38.p7 | 7:122529873 | TGGAAAGTTAACAAG[A/T]ATTGCACTATAATGT | 93664 |
rs138225280 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122447273 | TTTGTTTTTGATGTC[C/T]TCTCTTTATACACTT | 93664 |
rs138231134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122545215 | TCAATAGTTCTCTCA[A/G]AAATCAAGGGAGTGG | 93664 |
rs138241394 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122696719 | ATTCTGGGCTAAAAT[C/T]ATAATTTAATATTTT | 93664 |
rs138242624 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122761244 | AAGGAAAGAATTAAG[C/T]GAACGTTTCCATACA | 93664 |
rs138248541 | in-del | -/TCTT | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122652845 | AACAATAACAATTTG[-/TCTT]TCTATTATCCCTAAT | 93664 |
rs138250356 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122659813 | GAACTACATTAAACT[A/C]ATCAGAAATCATGCA | 93664 |
rs138250887 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122339955 | GCAAACAAGAGCATG[C/T]AAGTGCAAAATCAGT | 93664 |
rs138265230 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122432886 | ATTGTTACCCACTTT[G/T]AAAAGCATCACCCCA | 93664 |
rs138279456 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122781930 | TTTTGGGTGTCTTGA[C/T]ATTTACATGCTACTG | 93664 |
rs138279886 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122549932 | CAAATACTACCTCGA[C/T]GCAGCTAAGATTTTC | 93664 |
rs138281083 | snp | A/G | 0.0189856 | 0.0955633 | upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122886818 | GCCGCTGCTGCCCGG[A/G]CCCGCCTGGAGCCCT | 93664 |
rs138282411 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122463885 | GTTAAAGATAAGGAA[-/G]AAAAGCATGCTGAAA | 93664 |
rs138283094 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122626127 | AGATCACACAGGACT[A/G]GGGTAACAAAGACCA | 93664 |
rs138284424 | snp | A/C/G | 0.00268409 | 0.0365442 | intron-variant, synonymous-codon, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122701931 | AATGTTTGCAAGTTA[A/C/G]AATGCGTACTACATC | 93664 |
rs138301191 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122506571 | GGATTCTAGAGACCA[C/G]AGCATTCAGGTTTGT | 93664 |
rs138301983 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122816817 | GTAACTGAAGAATCA[C/T]AAAAGAAGTGAATAT | 93664 |
rs138307575 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122863321 | AGGCTCAAATAATTA[A/T]GAACAAGTTTTTGCC | 93664 |
rs138311082 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122726260 | AAAATTATCCTCCCA[A/G]TAAGTACTTTGATAA | 93664 |
rs138318731 | in-del | -/GGGGTG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122661050 | AAAGCTGGAGTGGCT[-/GGGGTG]GTATTAGCTTAAGAC | 93664 |
rs138328993 | snp | A/T | 8.16426e-05 | 0.00638864 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122360788 | ATAAAAAATACTTAC[A/T]GGAACATCAACATAT | 93664 |
rs138329102 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122327548 | GGTAAGTTGTATAAA[C/T]TTGAGGGAAATGAAA | 93664 |
rs138335164 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122453173 | AATATATCGACCACA[A/T]TTATTCCATCTGAAT | 93664 |
rs138341650 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122486397 | CAGGGATAACTTTAA[A/G]GGATTGAAGACTTGA | 93664 |
rs138344648 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122585049 | GGAAATGCTAACGAA[C/T]ACCTCCTGTGAAATG | 93664 |
rs138347661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122578616 | CAGGGCCACACCTGA[A/G]AACACCTGTCGGGCC | 93664 |
rs138372096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122735386 | CTAAATTTGTGCACT[C/T]TTTTTATTCATATAT | 93664 |
rs138385796 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122686586 | TCTAACAAGTTCCCA[C/G]GTGATGCTGAGGCTG | 93664 |
rs138396641 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122669625 | CCGTTCTCTTGGCCC[C/T]ACGTGTAGAGGACAA | 93664 |
rs138415135 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122623505 | TTGATTAAAGATTCC[A/G]GACAATAAAGCTACA | 93664 |
rs138417658 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122465176 | GAAGAATTGTAGATC[C/G]AGCAAAAAATACAAA | 93664 |
rs138422764 | in-del | -/A | 0.0215369 | 0.101512 | intron-variant | CADPS2 | GRCh38.p7 | 7:122416171 | CATGGTCTCTATATG[-/A]AAAAAAAATCATAAT | 93664 |
rs138427287 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122873687 | TTGGGTATATACCCA[A/G]TAATGAGATTGCTGG | 93664 |
rs138428194 | in-del | -/TAAC | 0.266819 | 0.249434 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554185 | CAGTCTATGGAAGTT[-/TAAC]TATTTCTAGGAACCT | 93664 |
rs138462119 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122401387 | TGGTCATTTGCCACT[A/T]GCTAGCATATCCACA | 93664 |
rs138472643 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122741258 | AGTCACCACTCACAT[A/T]GAAAATGGATAAATA | 93664 |
rs138477398 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122411823 | CTCTTGAGGGACAGA[C/T]GAATGAACAGGTGAC | 93664 |
rs138498203 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122673104 | GTCTTGCTGGCTTCC[A/G]GCTTCAGGAGTGAAG | 93664 |
rs138507246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122347413 | ATGATTTTTTGTTAC[A/G]AAGTTATTTCTGTGC | 93664 |
rs138510257 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122501009 | CCTGGAATCCCAGCA[C/T]TTTGGGAGGCTGAGG | 93664 |
rs138516397 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122546384 | AGGACCCTTATACCC[A/G]TATGTTAACATCTAT | 93664 |
rs138517975 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122361590 | GGAATCTAGTCACTA[C/T]ACATATGAGACCACT | 93664 |
rs138521819 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122514609 | AGGATAACATGTCAA[C/T]ACATCGAAATAGTCA | 93664 |
rs138524482 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122858308 | TTTGTCCTGCAATAT[A/G]CCCACAAACTCTCGA | 93664 |
rs138525176 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122606684 | TCTAAATAGTACAAA[A/G]AGTAGTATGATTAGA | 93664 |
rs138531135 | snp | A/G | 0.030665 | 0.119967 | intron-variant | CADPS2 | GRCh38.p7 | 7:122696513 | CATGACCCCATGGTC[A/G]TGGAAGCAGTTATAG | 93664 |
rs138543139 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122643933 | CCTCTCTACTAAAAA[G/T]GAAAAATTAACCAGG | 93664 |
rs138548435 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122368148 | CCTCCCAACGTACTG[A/G]GATTACAAGTGTGAG | 93664 |
rs138553281 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | CADPS2 | GRCh38.p7 | 7:122457940 | AAGACATTAAATTAA[A/G]TTAAATGCTCCCCCA | 93664 |
rs138564466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122551859 | GTTATTGCTTTGGTG[C/T]ATGATGGAATACTTG | 93664 |
rs138565325 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122725471 | ATATACTGCATGGAC[A/C]ATCTGGGCTTTTAGT | 93664 |
rs138566705 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122823802 | GTCTCTCTCCTCCAC[C/T]TGGCACCTGTTCACC | 93664 |
rs138575038 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122390971 | ATATACAGATACATA[G/T]GTCGATGAGCAATCC | 93664 |
rs138577550 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | CADPS2 | GRCh38.p7 | 7:122635268 | ACTATTAATGTGTGG[C/T]TAATTTTTTTTTTTA | 93664 |
rs138585960 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | CADPS2 | GRCh38.p7 | 7:122612258 | GAAGAAGTTAAACTA[C/T]CAGTATTTGCAGATG | 93664 |
rs138600538 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | CADPS2 | GRCh38.p7 | 7:122750279 | TATGTCATTTTTGTG[C/T]AATTATTTCATCATC | 93664 |
rs138600624 | snp | C/T | 1.65674e-05 | 0.00287809 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122702422 | TTATGTGTAAAAGTA[C/T]AGCCTCCACGTTCGA | 93664 |
rs138609116 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122331788 | ATTAAGCAATTTACT[C/T]ATTCAAGTTTATACA | 93664 |
rs138617867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122471591 | AAAGAATAGATATAC[A/G]TGTTTTTTCTTTCTA | 93664 |
rs138630525 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122794349 | CTTATTTCAGAAAGC[A/C]AGACTTCAAGCTCTG | 93664 |
rs138637116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122714894 | GTGAAGTAGACACTA[C/T]CAGAATCTCGTTTTA | 93664 |
rs138641773 | in-del | -/CAAGAAAACT | 0.299411 | 0.245069 | intron-variant | CADPS2 | GRCh38.p7 | 7:122752053 | CACAAAACAGATGTC[-/CAAGAAAACT]CAAGAACACTCAAAA | 93664 |
rs138669077 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122842626 | TGCTTACAGTATTGT[A/G]TAAGAAAAACAAATG | 93664 |
rs138674645 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122745848 | TCAACACACCACAAT[A/G]GATCAGAAAAGTCTA | 93664 |
rs138675663 | snp | C/G/T | 0.00239393 | 0.0345281 | intron-variant | CADPS2 | GRCh38.p7 | 7:122640195 | TAGAGTCATGTAGAG[C/G/T]GAAACCTAGAACCAC | 93664 |
rs138677404 | in-del | -/TA | 0.187685 | 0.242109 | intron-variant | CADPS2 | GRCh38.p7 | 7:122333890 | TTATAAATATAAATT[-/TA]TATATATATATATCA | 93664 |
rs138680644 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122810185 | GCTTCACCTCTAAAA[A/G]TAATTTAGGAAGAAG | 93664 |
rs138695640 | snp | C/T | 0.000424952 | 0.0145704 | intron-variant | CADPS2 | GRCh38.p7 | 7:122345539 | TTTGCAGTTTATCTA[C/T]GGTGTCAGCATACCT | 93664 |
rs138696501 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122526914 | ATCCTCATTGTCCAG[A/C]ACTGTTCCTTCATAT | 93664 |
rs138708037 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122482063 | AGCCACAGTCTTAAA[A/G]TTCTATGCTAGTGGT | 93664 |
rs138717646 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122494026 | ATGTGGCTGGGAAAG[-/T]TACTTCGTAGAAATG | 93664 |
rs138718063 | snp | C/T | 0.029116 | 0.117091 | intron-variant | CADPS2 | GRCh38.p7 | 7:122573663 | CCAAAATGTACTTTG[C/T]ACTCAAGAATACCAT | 93664 |
rs138724713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122376805 | GTGATGGTTTTATGA[C/T]TATAAACTTATATGG | 93664 |
rs138732441 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122734523 | TACTTGCACTGTTTA[C/T]TGCAAGGAGATATTG | 93664 |
rs138750237 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122422013 | CCAGCTAATGACTAT[A/G]TATCAGATGGATAAT | 93664 |
rs138750994 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122759872 | GAAGCAAAATCTAAA[C/T]AGGATTATTCCTAAG | 93664 |
rs138756016 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122681544 | ATTACTGTGTGAGTT[G/T]TGCAATTCACAGCAA | 93664 |
rs138756963 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | CADPS2 | GRCh38.p7 | 7:122345363 | GGCTAGTCTTGAACT[C/T]CTGACCTCAACTGAT | 93664 |
rs138765293 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122439892 | ATAACAAAAATGGCT[-/G]GTTAAAGTTAGAATG | 93664 |
rs138765322 | snp | A/G | 0.031825 | 0.122064 | intron-variant | CADPS2 | GRCh38.p7 | 7:122836347 | ATTGTAAAGACCACC[A/G]AGGCTGGGAAGAAAC | 93664 |
rs138784113 | in-del | -/TAT | 0.0505692 | 0.150756 | intron-variant | CADPS2 | GRCh38.p7 | 7:122493185 | AGAAATATAAAGAAC[-/TAT]TATAAATCAACAGGG | 93664 |
rs138786593 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122756636 | GGGCGCGGTGGCACA[C/T]GCCTGTAATCCCAGC | 93664 |
rs138792023 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122649736 | CATTACATTTCATAC[A/T]TCTATATGATTTATA | 93664 |
rs138802124 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122384959 | TGCCTACTGCATGTC[A/G]GGTACTGCAGTGTAT | 93664 |
rs138802690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122421457 | TCCTTTGCATCTAGG[C/T]CATGATGATCAGCTA | 93664 |
rs138802944 | snp | A/G | 0.000489716 | 0.0156403 | intron-variant | CADPS2 | GRCh38.p7 | 7:122441465 | TAACTAAAATACACA[A/G]CAACTGAGAAAGCAA | 93664 |
rs138805058 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122540408 | GTATCAAATTAAAGA[A/C]ACATTTAAAGTTTTA | 93664 |
rs138814633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122521736 | GAGCAAGAACTTAAA[A/G]TTTATGTGCTATATA | 93664 |
rs138836229 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CADPS2 | GRCh38.p7 | 7:122391093 | AATTCTTTATGTTAA[A/G]TATAAATGTTTCTTT | 93664 |
rs138838771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122622527 | TATTTAGATGGTGCC[A/G]AATCATTCTTAGAGA | 93664 |
rs138846449 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122583980 | CTGTAATTATAGTAG[A/T]TTACTCTATTGTCTT | 93664 |
rs138849025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122810617 | TTTAAGAAAGCAATA[C/T]AACCATTTATTCGCA | 93664 |
rs138852723 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122843138 | AAACAAAAGCCTTCA[C/T]TAAAAGGAGCAATGC | 93664 |
rs138857083 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | CADPS2 | GRCh38.p7 | 7:122690314 | GTGGTTCCCTTGGGT[C/G]CTGCACCCATGCCAA | 93664 |
rs138866337 | in-del | -/A | 0.198324 | 0.244601 | intron-variant | CADPS2 | GRCh38.p7 | 7:122655606 | TATGCAGTGTGAAAT[-/A]AAAAAAAATTGTGTG | 93664 |
rs138867054 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122372788 | CCGCATATTTTAATT[G/T]TTATGGGCTGGTTGC | 93664 |
rs138867071 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122425577 | CACCAGTGCACTCCA[C/G]CCTAGGTGACAGAGT | 93664 |
rs138867812 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122794307 | TTCATTTCCTTCTCA[-/T]TTTTTTCTGTACTCT | 93664 |
rs138880754 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122433683 | GCTGGAATTACAGGC[A/G]TGAGCCATTGTGACT | 93664 |
rs138884460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122536992 | ACATGGGCACATAGA[A/G]GAGAAGACCACATAC | 93664 |
rs138888258 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122588121 | TATTAGACCTTGCTC[A/G]AATGGATGGATTGCA | 93664 |
rs138889437 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122568621 | AAAGCATTTCAACAG[A/G]CTGTGCTAGAACAAC | 93664 |
rs138894170 | snp | A/C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122860666 | CACTCTACTATGCAA[A/C/T]AGAATATCAGGATTT | 93664 |
rs138901276 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CADPS2 | GRCh38.p7 | 7:122879748 | ACTTGAAGGTATAAA[A/G]TGAAAGTACTGAAAC | 93664 |
rs138906131 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | CADPS2 | GRCh38.p7 | 7:122664626 | ATGCTGTCAATATTC[C/G]TAAGAATCCTCCATA | 93664 |
rs138919927 | in-del | -/AC | 0.0252325 | 0.109451 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122700888 | CTATAATAATTTAGA[-/AC]ACTTTTCCTTACATA | 93664 |
rs138920671 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122555265 | TTATAATGACTGAAA[A/C]AAAGTAATTATTTTT | 93664 |
rs138921975 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122697014 | ATTAAACATTTTATT[C/T]AAGAAAACAAATTGG | 93664 |
rs138967459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122828413 | ATTTTTAAGATAATT[A/G]TTGAGATGTTCATAT | 93664 |
rs138968099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122627101 | AGGATGTTAAGAGAG[C/T]GAGCCCAGGCTCTGG | 93664 |
rs138984603 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122770626 | TGTTTCCTCTTCAAA[C/T]TAGTGCCCAGTACAG | 93664 |
rs138985557 | in-del | -/TGATGGTAA | 0.311123 | 0.242413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122814211 | ATCAAGCAGAGGTTT[-/TGATGGTAA]TAACGTGACTAGTAA | 93664 |
rs139005848 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122781206 | TGTCCTTTGAACTAT[A/T]TTTGGTTTTTACCCA | 93664 |
rs139008096 | in-del | -/AT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122720434 | TGTATATATATATAC[-/AT]ATATATGTATACATA | 93664 |
rs139011944 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CADPS2, RNF148 | GRCh38.p7 | 7:122701481 | GCATTTGGAGATATA[C/T]CTAATGTTAAATGAC | 93664 |
rs139012080 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122656244 | AATAGTGAGGATCCA[A/G]AAAAGATCCCTGTAT | 93664 |
rs139017855 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122371628 | ATCAAGGGTGAAGTG[A/G]GGGACCATGGTGGAG | 93664 |
rs139031478 | in-del | -/TT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122636482 | TTTTTTTTTTTTTTT[-/TT]GAGATGGAGTCTCAC | 93664 |
rs139032335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122484524 | GTTGTAAAATGTAAA[C/T]GCCAAAATTGTAAAA | 93664 |
rs139035659 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122851684 | CAAAGGGACAACTTA[C/T]ATGGCAACAGTCAAG | 93664 |
rs139042386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122777041 | CTGTAGTCCCAGCTA[C/T]TCACGAGGTTGAGGC | 93664 |
rs139042832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122824134 | TAAAAGAAATAAAGT[C/T]GAAAAAAATATAGAT | 93664 |
rs139044897 | snp | C/G | 0.181659 | 0.240478 | intron-variant | CADPS2 | GRCh38.p7 | 7:122737278 | CTTCCAGGCTGGAGT[C/G]CAGTGGTGCGATCTC | 93664 |
rs139051358 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122766052 | GGAACCCCTTCTGGT[A/G]AGGGTCTCATGCTGC | 93664 |
rs139100812 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122767841 | GTTTTATAGTAGAAC[A/G]TAGATGATCTGCATT | 93664 |
rs139107607 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122497017 | CTGGGATTGTTACTT[C/T]TTTCTCGGACTGTTC | 93664 |
rs139110856 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122813667 | CATTCTGACAATTTC[A/T]TTGCATAAAAACCGC | 93664 |
rs139116118 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122624267 | CTAGTTGTCTAACTG[C/T]GAGTCACTCTTACAA | 93664 |
rs139120260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122692220 | TACTTGCTTGACTCC[C/T]GCAACATAGCGGGGG | 93664 |
rs139124770 | in-del | -/TA | 0.17654 | 0.238964 | intron-variant | CADPS2 | GRCh38.p7 | 7:122706628 | GTGTATATATATATA[-/TA]GTTACATGCTCTTAA | 93664 |
rs139129648 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122726152 | ATAAGATTCTCCATA[C/G]TGTCTTATAGAAACT | 93664 |
rs139130136 | in-del | -/A | 0.361613 | 0.224595 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554697 | ATATCACCTGTATGG[-/A]AAAAAAAAACCCACA | 93664 |
rs139133692 | in-del | -/G | 0.0150606 | 0.0854603 | intron-variant | CADPS2 | GRCh38.p7 | 7:122735733 | AAATATAAGCCTACT[-/G]TTTCACTAAAAACTT | 93664 |
rs139136753 | in-del | -/GT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122725371 | TATATATGCATATGC[-/GT]GTGTGTGTGTATATG | 93664 |
rs139137625 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | CADPS2 | GRCh38.p7 | 7:122650246 | AAAAGAAAAAATATA[A/T]ATCAAATATATAATT | 93664 |
rs139146798 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122397926 | GAGGGGAAAGCCAGC[A/C]CCTATTTTTCAGATA | 93664 |
rs139150806 | snp | C/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122742765 | GAGCCACTGTTCTAG[C/T]TAAGAATTATTTTGG | 93664 |
rs139151184 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122454568 | GTCTAAGGTGGAGAC[A/G]TTAAAAACCAATGAC | 93664 |
rs139152020 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122400517 | ACAGTACTGTGGAAT[C/T]CAACTGAGGGGAAAA | 93664 |
rs139161123 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122553258 | GCAATAATATCACAT[A/T]AAAGTTTGTCCTAGT | 93664 |
rs139174564 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122727844 | TGCCATCCTTAGAAT[A/G]TAAGAAAATATGAAG | 93664 |
rs139181771 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122857384 | AAAGAAACAAAAAAT[A/T]GTAAAAACTGAAAAA | 93664 |
rs139182334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122557794 | TGCTTTCACCAGTAT[A/G]GAACTGTTGCTAGTA | 93664 |
rs139183081 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122869599 | AATGTGTCATTCAAG[C/G]TAAAGGAGAAGATCA | 93664 |
rs139202073 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122821022 | TGACGCATATACTTT[C/T]TGCTTCCTGGCTCCT | 93664 |
rs139211732 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122408405 | GCTCACATCCATTCT[C/T]CATTCAGCAGCCAGT | 93664 |
rs139214072 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122355465 | ACATGCCTGTTTTCC[C/T]GGCTACTTCGGAAGC | 93664 |
rs139216422 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122504049 | GGTTTAACAGATCAA[C/T]CTGCTATGTCAAATG | 93664 |
rs139221876 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122447943 | AAGGAACATTTTTTT[C/T]AGTGCATGTCTAAAA | 93664 |
rs139223874 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122628898 | TGTATTATATGATTT[A/T]GCGGGGAGGAGTTTT | 93664 |
rs139237006 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | CADPS2 | GRCh38.p7 | 7:122861026 | CATTTAAGTAGATTT[A/C]CATGTCTTGACTATT | 93664 |
rs139240884 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122772870 | AGGTAAAAATCTAAG[C/T]TCTTGACAGAGAAGG | 93664 |
rs139256960 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122670215 | CATTTAAATCCTTCT[C/G]CAGCTTAAAATTTTT | 93664 |
rs139272389 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122713336 | AGCTCTACAACTTAG[A/G]CAACCTATCTAAACT | 93664 |
rs139278915 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122378651 | TTGATGAAGCCTTGT[C/G]AGAGCATGGGATATA | 93664 |
rs139286870 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122517360 | TAAAGCTATTATGAA[C/T]ACTTGTGTACAAGTC | 93664 |
rs139287094 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122834971 | TTTGAGAACTGAGAA[C/T]GGACAGACTGCCTCC | 93664 |
rs139291145 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | CADPS2 | GRCh38.p7 | 7:122452686 | CAGGGGTGAGCCACC[A/G]TGCCCAGCTTAGCTT | 93664 |
rs139297795 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122719469 | TGGCATGTGCAATGA[C/T]GCCAATTTGAAAAAC | 93664 |
rs139298467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122449588 | AAAGTGCTGGGATTA[C/T]AGGTTTGAGCTACCA | 93664 |
rs139300109 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122496061 | CCTTTTTAATGTTTT[C/T]GAGAAATGTTATTGC | 93664 |
rs139303150 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122548562 | TAGACTGGTAGAGCT[A/G]TATGGATCAAATCAT | 93664 |
rs139310355 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122589253 | GTATTATCTCCTTTT[A/G]ATTGAATAATGTAAC | 93664 |
rs139310733 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122638475 | CACAGGGGTTTAGCA[A/G/T]GTTTTCTGTCAAGAG | 93664 |
rs139313435 | snp | A/C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122795647 | TGTAGAAAAAACTTT[A/C/T]GATAAAATTCAACAC | 93664 |
rs139321709 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122715462 | AACTGACACAGGATT[C/T]CCGTGCCTTGTAATT | 93664 |
rs139334347 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122687937 | TCTCATTTAATTAGT[C/T]TAAGTATAGACCTAT | 93664 |
rs139354631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122537234 | GAAGTATATTTACAA[C/T]TATTTGTCCTAGGTT | 93664 |
rs139380540 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122762014 | TGAGACTCTGCCTCA[-/A]AAAAAAAAAAAAAAA | 93664 |
rs139381697 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122385135 | ATGAGGAGGTAAATA[A/G]GAGCCACTGGTATCT | 93664 |
rs139396748 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122753185 | TAAAATCTAGTAGGG[A/T]ATAATTAAGTCAAAG | 93664 |
rs139405042 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122647423 | AGAATCATGAAAATA[C/G]TTTGCACGTAGGCAA | 93664 |
rs139432023 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122766915 | TTTCCTACATATGAG[A/G]TAGGAATAACAATAG | 93664 |
rs139438283 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122657353 | CTGTGAAGAAAGTCA[C/T]TGGTAGCTTGATGGG | 93664 |
rs139448791 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | CADPS2 | GRCh38.p7 | 7:122597289 | CTCACATAATTACTC[A/G]GAAAAAGAAATCAGT | 93664 |
rs139449834 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122542031 | ATAAATTATCTATTG[C/T]GTAATGATAACAGCT | 93664 |
rs139455607 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122397257 | ATTTCCTATGAACTA[C/T]AAAAAATCTTAAATT | 93664 |
rs139460850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122865322 | ATAAATTGCCCAGCC[C/T]CAGGTATTTCTTTAC | 93664 |
rs139461271 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122627295 | AGCAAGGTCAGTCAA[C/T]TGTTATTAGGCTTAA | 93664 |
rs139463795 | snp | A/C | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122533490 | ATCAACAAACTCACA[A/C]TGCTTAACGGAAGGA | 93664 |
rs139466959 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | CADPS2 | GRCh38.p7 | 7:122778167 | TCTCAGATGGAGATA[A/C]GGAACCTGTTGGAAG | 93664 |
rs139467709 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122619281 | AAGATAATGGTAGAT[C/T]TGTAAATTATAAAAG | 93664 |
rs139506128 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122876056 | CCAGGTACAGTGGCT[C/T]ATGCCTGTAATCCCA | 93664 |
rs139518383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122789944 | ATTTTCTTAGAAAAA[C/T]GAACTATAAAGACAG | 93664 |
rs139525710 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122449286 | AAAATACATTTAAAG[G/T]ATTCTATACAACCTA | 93664 |
rs139533088 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122850064 | TGAAGACCTGGGGGC[C/T]TTGCTTGGCAACAGC | 93664 |
rs139533223 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122546742 | CTGAAATCTTTGCAA[A/G]TCTTGGTACTGTCAG | 93664 |
rs139543287 | snp | C/T | 0.0700422 | 0.173537 | intron-variant | CADPS2 | GRCh38.p7 | 7:122660815 | CTTGGGAGGCTGAGG[C/T]AGAAGAATCACCTGA | 93664 |
rs139572561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122482603 | AAAAAGTTTATTAAA[C/T]GCTGCACGTTGGGCA | 93664 |
rs139576419 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122704657 | AGCTCATTCATTCTA[C/T]TTTTCTCATTATAAT | 93664 |
rs139584925 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122574590 | AGTACAAGTTGAGCC[C/T]CTAAAATTTCATGTC | 93664 |
rs139592056 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539199 | GACCTTTAAGATCAC[A/T]AAGGACTCTGCCCTC | 93664 |
rs139601538 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122509759 | GTAAGTTCCATAACC[C/T]CTCTGTATTATTTTC | 93664 |
rs139603503 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122671094 | AGATCCTGTATCGTA[C/T]GCTGTTACAGGACCT | 93664 |
rs139628299 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122320547 | TACAATTACTATGAC[A/T]ACATCAAAATGTTGT | 93664 |
rs139629011 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122327427 | AGTTATTTTGCAAGG[G/T]ATAGTAAATATTTCT | 93664 |
rs139632948 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | CADPS2 | GRCh38.p7 | 7:122422914 | CAGTGAGCCGAGATC[A/G]CGCCACTGCACCCCA | 93664 |
rs139634637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122362497 | TTATATTTCTATGAA[A/G]TAAAAAAACACATAC | 93664 |
rs139638234 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122880683 | TACAACCTGGATAAT[A/G]AGATTGTTTTTAAAG | 93664 |
rs139640572 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122455064 | AAGCCAAAGCCTTTA[C/T]AATGATGTATGAGCC | 93664 |
rs139646700 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122797589 | TCCTTAGCAAACTAA[C/T]GCAGGAATGGAAAAC | 93664 |
rs139661346 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122830483 | ATAACATGCAACAAT[A/T]TTAAAATAAGCAAAC | 93664 |
rs139684901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122473583 | TAAGGGATAGTCAAC[C/T]TGTACTATGCTCAGT | 93664 |
rs139708702 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122731535 | AACTGCAGAGTCAGA[A/T]GATGTTTCCTAAATT | 93664 |
rs139714881 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122325904 | AACAAAGGATCCTAA[A/C]TACATGTTATAGGAC | 93664 |
rs139718044 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122657235 | TATAGTTTGAAATCA[A/G]GTAGCGTGATGCCTC | 93664 |
rs139723771 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122460408 | AGCCATAGACCTAAT[C/T]TGGATGAGCTGCTAA | 93664 |
rs139731373 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122321693 | CTCTATCGGCCAGAC[A/T]GATCTCAAACTCCTG | 93664 |
rs139733108 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122875127 | AGTGTGTATACGTTT[A/G]CAGATGTGTACACGT | 93664 |
rs139737102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122467524 | ATAATCTGGAATCCA[C/T]AGAAAATTGAGATTA | 93664 |
rs139738019 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122784138 | AAATTATTTTTCCCA[C/T]CATGACCCACTATTT | 93664 |
rs139745194 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122788193 | AAGTGTCTTAACAAC[C/T]CCTTTCTTTGTCTAC | 93664 |
rs139748837 | in-del | -/AAAC | | | utr-variant-3-prime | CADPS2 | GRCh38.p7 | 7:122319951 | TGCTCTTCTCCAAAA[-/AAAC]AAACAAACAAACAAA | 93664 |
rs139751883 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122703108 | AATGAGTCAAGATAC[A/G]TAACAATTTGAATAG | 93664 |
rs139774827 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122532272 | CAGTTGCACAATCAC[A/G]GGCAAAAAAATTACC | 93664 |
rs139775715 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122373632 | TGTTTTTCCAAAGGT[A/G]CAGATACCAATGTAA | 93664 |
rs139780316 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122618775 | GCTTGGCTGATGTCA[C/T]AGGTCCTGTGACTAG | 93664 |
rs139782792 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122447869 | GTTTCAGGGATCTTA[A/G]ATCCTCTTTGTTTCC | 93664 |
rs139787495 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122465703 | AACCGGTCGCTGGTG[A/C]CAAAAAGGTTGAGGA | 93664 |
rs139796264 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122413230 | CTTTTAGATGGAGAG[A/T]TGTCAGATCAGTTTG | 93664 |
rs139801803 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122834347 | AGGAACAGCTCCAGT[C/T]TACAGCTCCCAGCGT | 93664 |
rs139812054 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817639 | CAAGTCCTGCTTTTC[C/T]GGGAAAGGGGCAAGT | 93664 |
rs139814825 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122699799 | TTAATCAAACAATAT[G/T]TTGAAAGAGGAGGAG | 93664 |
rs139824889 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122683506 | AATACTTTTTGTTTC[A/G]TAACAATTTTATATA | 93664 |
rs139842821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122503834 | AAAAAAGCCATCTCA[C/T]AGAGTGAGAATGGAG | 93664 |
rs139852087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122767453 | TTATTTCCTCAGAGA[C/T]CATAGTTGTGCCAAC | 93664 |
rs139856083 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122688835 | TGACAAAAGCACAGC[C/T]ATGTTCCTTACACTC | 93664 |
rs139859024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122466176 | TATAGTCTAATATAT[A/G]CTAAAAAATTTCCTT | 93664 |
rs139865296 | in-del | -/T | 0.0532157 | 0.154195 | intron-variant | CADPS2 | GRCh38.p7 | 7:122434849 | TAATAGCATTTATGC[-/T]TTTTTATTCTGTTAT | 93664 |
rs139869727 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122357058 | GCATGCATATACATA[A/T]ATCTAAAAATACTGT | 93664 |
rs139872897 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122562986 | TCCACACAACCTAAC[A/G]ATTAAGAATTATTTC | 93664 |
rs139882955 | snp | C/G | 0.312593 | 0.242037 | intron-variant | CADPS2 | GRCh38.p7 | 7:122820044 | ACCAGACAAGCCTTA[C/G]AAGTTAGTTCAGGAT | 93664 |
rs139887898 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | CADPS2 | GRCh38.p7 | 7:122614645 | AATTTAATTAACTCA[C/T]TGCCAGAACCTGAAA | 93664 |
rs139917331 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122499131 | TTAAAAATTCTGAGG[G/T]TTAATTTTCCTGCAT | 93664 |
rs139917368 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122557094 | GCACGTGTAACAAGG[A/G]GAGGTCCACAGATAC | 93664 |
rs139922125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122334795 | CATTTAAAAAAAAAT[C/T]TGTGGATAGCTATTC | 93664 |
rs139924657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122751183 | AGGGTCTGCCTATGT[C/T]GCCCAGGCTGTTCTC | 93664 |
rs139935534 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122867227 | TCTGTTGCTTAATCC[A/G]TCTCCTCTACTAGAA | 93664 |
rs139943987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122406708 | ACAGAAGACAACTGT[C/T]GCATTGATCAAAGAG | 93664 |
rs139947918 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122609455 | GTTTACTAAGAGACT[A/G]TGAAACAATGACTTA | 93664 |
rs139952661 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122798362 | AGTGTATAAACTTCA[C/T]CACAGTCTAACTAGG | 93664 |
rs139960407 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122634349 | TGATTCAATTTCAGC[A/G]TTTGTTACTGGTCTG | 93664 |
rs139964451 | in-del | -/AT | 0.20511 | 0.245937 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554880 | TTATTTTTTTGACAA[-/AT]ATGTGTTTTCACATT | 93664 |
rs139971621 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122684511 | CTATTTGTTCTTTCA[C/T]GTATCAACCCAATCC | 93664 |
rs139978599 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122871472 | AGTATTCCCCCCCAC[-/A]AAAAAAAAAACAGGA | 93664 |
rs139980482 | snp | A/G | 9.8925e-05 | 0.00703226 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698258 | ATCGCTGCCATCTCC[A/G]GTTCTGAATCCTTGC | 93664 |
rs139986410 | in-del | -/TA | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122651060 | TTTGAGATTTTAAAT[-/TA]TATATATATATGAGA | 93664 |
rs139988182 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122553758 | ACCTCTATGTCTGTT[G/T]CTACTAACTCAGGGT | 93664 |
rs139992540 | in-del | -/A | 0.158632 | 0.232706 | intron-variant | CADPS2 | GRCh38.p7 | 7:122659871 | AGAGCGCTGAAAGAG[-/A]AAAAAAAAATCTAAC | 93664 |
rs139993330 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122636709 | GACCTGATGTGATCC[A/G]CCTGCCTCGGTATCC | 93664 |
rs140006673 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122461174 | ATTGAAAACATTACA[C/G]AGGATGCAGCTGGAA | 93664 |
rs140015772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122843618 | ATGACATTATATGCC[A/G]GATTGTGACATTTGA | 93664 |
rs140016468 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122558269 | AGATTGTGTCTGATG[C/T]TGACAGTCATAATAA | 93664 |
rs140018558 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122614430 | ACAGGTCACATATTG[A/G]TATTATAATAAGGCA | 93664 |
rs140021362 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122835417 | TCCTCGCCAGCAATG[C/G]AACAAAGCTGGATGG | 93664 |
rs140039938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122727373 | GTTATTGGCAGCTAC[C/T]TAGCTTGGGTTAAAT | 93664 |
rs140051658 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122375177 | TAATGGCATTTTTTT[A/T]AAAGTAACAGAAAAA | 93664 |
rs140052401 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122428892 | ACTATCTGCATCCAG[A/G]GCCTCTCTCCTCCCC | 93664 |
rs140054405 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122612457 | AATAGCATAAAAAAG[A/G]ATAAAATAATAGAAA | 93664 |
rs140056297 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122531652 | GTTTCCTAATTGCTT[A/C]AAAGAATTATCCAGA | 93664 |
rs140061581 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122342816 | AGGAAATACTCTAAT[C/T]GGAATAGCAAAAGTT | 93664 |
rs140066464 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | CADPS2 | GRCh38.p7 | 7:122711407 | ATGAGCCCCAAAGAG[A/T]CATTATTAAGAGAAA | 93664 |
rs140078811 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122847728 | ATTGTGAAGATTCAG[C/T]GCAAACCCACATAGT | 93664 |
rs140086805 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122380083 | GTTTTATTACCGCTT[C/T]CTCATGAAAAAGATG | 93664 |
rs140095397 | in-del | -/A | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122516716 | ATAATGTTAGGTTTT[-/A]AAAAAGCAGTCATAC | 93664 |
rs140097289 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122838841 | TCAATATCGTGAAAA[C/T]GGTCATACTGCCCAA | 93664 |
rs140106790 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122651789 | GGGTCTAGATAGCTA[C/T]AAAATTTAGTTACTT | 93664 |
rs140125205 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122423460 | TGCCTCAAAATCTGG[C/G]GGTGAGGTGGTTCCC | 93664 |
rs140129163 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122524544 | GAGGAATACTCAGTT[A/C]AACAAAACTAAGCAA | 93664 |
rs140135343 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122771488 | TATTTAGGAGGCACA[C/T]TGAATAAGATGAATA | 93664 |
rs140139893 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122884700 | TTTTTTTCTAAGAGG[A/G]TAGATCTTAAGCATA | 93664 |
rs140140123 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122691586 | AACCAGAGGTTCGCA[C/T]AACGTCATCAACAAG | 93664 |
rs140140160 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122647821 | AAACAAAGTCTAATG[C/T]TATGAGCCTGACATA | 93664 |
rs140140875 | snp | C/T | 0.00185501 | 0.0303984 | intron-variant | CADPS2 | GRCh38.p7 | 7:122393349 | CGTGGGAAGGGACCA[C/T]CATAAGCGATAACTA | 93664 |
rs140144844 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122488527 | GGACACAGACTACAT[A/G]GACTTCATTGCCAGG | 93664 |
rs140149864 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | CADPS2 | GRCh38.p7 | 7:122878126 | CTGGGCGTGGTGGTA[C/T]GTGCCTGTAATCCCA | 93664 |
rs140160140 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122882379 | GTTCTATTTTAATAC[C/T]CTCTTATTTCTAGTT | 93664 |
rs140160879 | in-del | -/AGA | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122777735 | CTTGCAGCCACCTTG[-/AGA]AGAAGAGCATGTTTG | 93664 |
rs140164727 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | CADPS2 | GRCh38.p7 | 7:122470058 | GCAGATGGAAGAGGA[C/T]GGTAATGGGAAAATG | 93664 |
rs140166569 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122571293 | CCATAATGAAATAAC[A/T]ATATATACCTATTAG | 93664 |
rs140169190 | snp | A/G | 0.210301 | 0.246828 | intron-variant | CADPS2 | GRCh38.p7 | 7:122723729 | aagacacatgcacac[A/G]tatgtttattgtggc | 93664 |
rs140173598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122565792 | GTGTATGTACTGAGA[A/G]CATTTAAGATATATT | 93664 |
rs140173609 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | CADPS2 | GRCh38.p7 | 7:122681248 | TGAACCTGCACAATG[C/T]GCACATGTACCCTAA | 93664 |
rs140174955 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122448929 | AGGTGTGAGATAAAG[-/A]AAAAAAAAATAAAAA | 93664 |
rs140186068 | in-del | -/CAAGGAATGCAAGGTT | 0.0158469 | 0.0875917 | intron-variant | CADPS2 | GRCh38.p7 | 7:122611881 | ATAGTGGGAATTGTG[-/CAAGGAATGCAAGGTT]CATTTAACACCTGAA | 93664 |
rs140199836 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122575009 | TTTGATAAGATGCAA[C/T]GGGAAGCACAAAACA | 93664 |
rs140208467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122397018 | GTATACGCCTCATAC[C/T]TTGTATAAAATATAT | 93664 |
rs140210157 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122335918 | TCCAATGAGAGAAAA[A/C]AGAGAAATGGGTTTA | 93664 |
rs140225701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122853328 | GCCCCCTGTGGGGTA[C/T]ACCCTCCATGGTTCC | 93664 |
rs140231676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122806981 | GCTGAACACTAGAAG[C/T]AAGCATTCCTCCTTT | 93664 |
rs140236573 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | CADPS2 | GRCh38.p7 | 7:122721957 | ACATGATTATCTCAA[C/T]AGATGCAGAAAAGGC | 93664 |
rs140237671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122520377 | TCATATGTAATATTC[C/T]GATTTCTTTTCTTTT | 93664 |
rs140240001 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122720701 | ATATACCCCTAAAAA[A/G]GATATACCTCCTGTA | 93664 |
rs140241486 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122610860 | TACACTAGTGTTCTT[C/T]CAATGGGTTTCAGAA | 93664 |
rs140270721 | in-del | -/CAT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122423764 | ACACAAATTGCTTGG[-/CAT]CATCATTCCGAATTT | 93664 |
rs140283631 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122862152 | TAGGAAGGCTACAGG[A/G]AGGACATATCTGCAG | 93664 |
rs140289910 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122492351 | GTCTGCCTCTTAATT[A/C]TTCTTGTCTTTTGGA | 93664 |
rs140295079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122489973 | CTATTTTCATTTAAT[C/T]AGGAATCAATTAATG | 93664 |
rs140296437 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | CADPS2 | GRCh38.p7 | 7:122585322 | AATCCCAACATTCCA[C/T]GATACAGGCATAAAT | 93664 |
rs140305789 | in-del | -/C | 0.351853 | 0.228311 | intron-variant | CADPS2 | GRCh38.p7 | 7:122658369 | AGAAATACCATTCGA[-/C]CCAGCCATCCCATTA | 93664 |
rs140311276 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122724594 | TAACTGGTTCAATCA[C/T]CAACCATCCTTGGAG | 93664 |
rs140314206 | snp | A/G | 3.29522e-05 | 0.00405894 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698581 | ACTTTAATTTTCTGT[A/G]TGAAGGTACAACCTC | 93664 |
rs140314598 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | CADPS2 | GRCh38.p7 | 7:122606706 | ATGATTAGAGTACTG[A/C]GTGCCTACTGAGCCA | 93664 |
rs140314639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122648173 | TGATGCCTCACTCTC[C/T]AGTTCTTCTCCCACC | 93664 |
rs140315159 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | CADPS2 | GRCh38.p7 | 7:122617158 | TACTGTAAACATGAC[C/G]TCCTAAAACATACAA | 93664 |
rs140329176 | snp | C/T | 4.95127e-05 | 0.00497533 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698699 | CTGGTGGCACTATAA[C/T]TCCTGCCACTCTCTT | 93664 |
rs140337913 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122394723 | GGCAGCCCATGGCAG[A/G]GTCTAGATCCTAGGA | 93664 |
rs140347053 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122343299 | AATACAAAACCTTCA[C/G]AACCAAAACAGAATG | 93664 |
rs140351965 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122345511 | AACATACCATCAAAA[G/T]TCAACTTTTCTCTTT | 93664 |
rs140357959 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122802386 | TCCTGTTCCCTCTGC[A/G]TCACATGCTGTGTAC | 93664 |
rs140373482 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122850269 | CTCCACTGGGGGCCC[C/T]AGGACTCCCCAGCAG | 93664 |
rs140374843 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122627993 | CAAAAATAAGGCATG[A/C]TATCCTTTCAATCAC | 93664 |
rs140377486 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122439804 | GTGATTATTACTAAA[C/T]TTTAAGATTAATTTT | 93664 |
rs140377714 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122763052 | CAGATATGTTTCTTG[G/T]ATATGATCAACTTTG | 93664 |
rs140377786 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122685827 | TGTCTTCCTCCTTGA[A/G]TGTAAGATCTTACCC | 93664 |
rs140430113 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122844659 | ATCTATAGTAATGTA[C/T]CCTAAGTTACATAGT | 93664 |
rs140431235 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122489282 | AGAATAGTTACTTGA[G/T]GCATGAAAAGCAGAA | 93664 |
rs140432159 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122446165 | ATAGTCCTTCTAATA[C/T]ATTTGGTTTACTAAT | 93664 |
rs140438100 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122759893 | TATTCCTAAGTGAGC[A/G]TATAAAATAGAAGCC | 93664 |
rs140440934 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122826682 | ATCAAAATAAAAATG[A/C]ATTGGTTGGACTCAG | 93664 |
rs140441168 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122632639 | ATTTTCTCCCATTCT[A/G]TAGGCTGTTGGTTGA | 93664 |
rs140441174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122581166 | CTGGACACACAGGCT[A/G]ACCACAACTCACCCT | 93664 |
rs140441716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122354489 | AAGTACTCCATATTA[C/T]TGTCAAACATGATCT | 93664 |
rs140442291 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122543364 | TAGCTCTACTGTATC[C/T]AATGCATTACTCTTG | 93664 |
rs140445832 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122446799 | AGTCCACTAGGCTCT[A/G]CCTAGGTTCCTCCTT | 93664 |
rs140460210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122625444 | AGATATTCTTTAGAC[A/G]TGAATAACATTTACA | 93664 |
rs140486577 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122654066 | ATAAGAAGAGACGGG[C/T]CAAATGCTAGGCCTC | 93664 |
rs140488749 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122637636 | GAGCTTTGTTGCTAC[C/T]CAGATTCTGAATTCT | 93664 |
rs140506007 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122369536 | CCTTTTTTCAATTGT[C/T]GAAATCTTATAATCA | 93664 |
rs140510928 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122740494 | ATATGACATTCTGGA[A/C]AAGGCAAAGCTATGG | 93664 |
rs140514039 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122775208 | ATGTTTGTGAAGAGT[C/T]TAAGAGTCTAAGCCT | 93664 |
rs140515369 | in-del | -/A | 0.469346 | 0.119947 | intron-variant | CADPS2 | GRCh38.p7 | 7:122322037 | CAGAACCAGTGAGAT[-/A]AATTCTGAAAGGTAT | 93664 |
rs140517763 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122500408 | AGCCACATATTTATC[A/G]TCTTAAAAAAAAACT | 93664 |
rs140518610 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122544694 | GAGAGGAAGTGAAAA[C/T]GCACATGTGCTTTTT | 93664 |
rs140519883 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122696302 | TAACACTTAGTGTTC[C/T]TGCTAAATCCTCCAG | 93664 |
rs140522084 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | CADPS2 | GRCh38.p7 | 7:122590709 | GATTGATTCATAAAA[A/G]AATTTACCTATCTAG | 93664 |
rs140547536 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122832764 | TAGTGGAGAAATCAC[A/T]GTACAATATGGGAAC | 93664 |
rs140558998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122642532 | CATAAAATAACTACT[A/G]AGTTTCACCCAACAG | 93664 |
rs140564667 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122412870 | GACAGAATGGAAAGG[C/G]ACATCACCAGGTTTG | 93664 |
rs140581870 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122829977 | TGTATAAAATGAGGT[A/G]TACTATATAACTATT | 93664 |
rs140584200 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122424055 | AGTGTCCACATTTGG[A/G]CAATCCTATATATAA | 93664 |
rs140587920 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122694256 | CAATTAAGGGAAACT[G/T]CTTGGAATGAGAACC | 93664 |
rs140590019 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122742586 | TGAGAGGGCCACTTC[C/T]CACATTCTAAGCATT | 93664 |
rs140591547 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122559397 | AGTCCGTTTCCACCG[C/T]TCTCCACGAAAAGAA | 93664 |
rs140598326 | in-del | -/G | 0.0614824 | 0.164198 | intron-variant | CADPS2 | GRCh38.p7 | 7:122424848 | TGAAGGCTTGAGGGA[-/G]AAGAAAGTTTTCTAT | 93664 |
rs140607225 | in-del | -/TTCCC | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122437589 | CATTAACTGCATTTT[-/TTCCC]TCTATTAGTTAATCC | 93664 |
rs140623603 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122417248 | CTCATTCATTAAATA[C/T]TCATTATATACTCAC | 93664 |
rs140628849 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122410637 | CTTGCCCTAACCTCT[C/G]CCAGTGTTGCTGTGA | 93664 |
rs140632347 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122743449 | AGCAACCATGGCTGC[A/G]TGGAGCCTGCCCTGA | 93664 |
rs140633312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122540462 | TAGATCATTTTAACA[A/G]AGTCTGTTGTGGGTA | 93664 |
rs140635741 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122667051 | GAGTTTTCTTTACCC[A/G]TACTAACCAATTTGT | 93664 |
rs140643000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122506479 | CTGCATCTGGTATAC[A/G]AAACCTCCCATTTTG | 93664 |
rs140646216 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122874291 | ACTCACAATTGCTAC[A/G]AAGAGAATAAAACAT | 93664 |
rs140646444 | in-del | -/AGAGAACTATG | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122430908 | AACTATGATGATGGA[-/AGAGAACTATG]AGTCACAATTAAGCA | 93664 |
rs140646964 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122502963 | AGATTTTCAGCCATA[A/G]CACTTATTTCATAAG | 93664 |
rs140648043 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122824420 | TTTGTTTTCTTGAAG[C/T]TCTGCCAGCAACAAA | 93664 |
rs140691736 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122871631 | ATGTCTGAAAACGTG[A/G]CTTGTGTGAAATAGA | 93664 |
rs140696938 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122371785 | TGTGTGATGTGCTTG[A/C]GCAGATTCTATAAAG | 93664 |
rs140697888 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122785224 | GTTCACGTCTCCTCC[A/G]ACATTGCTACTTCAC | 93664 |
rs140699926 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122463681 | TAACCTCACTAAGGA[C/G]GGTGGGAGAAAAAGC | 93664 |
rs140709071 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122517001 | ACCACAATCAACTTA[C/T]AGAACATTTCCACCT | 93664 |
rs140715481 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122608952 | CAGCACTTTGGGAAG[C/G]TGAGGTGGGAGGATT | 93664 |
rs140725417 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122868513 | CTAATTTCCTAGGAG[C/G]CACTAAGAACAAAGA | 93664 |
rs140726835 | snp | A/G/T | 0.0127068 | 0.0787735 | intron-variant | CADPS2 | GRCh38.p7 | 7:122720416 | GATAACTTAATAGAG[A/G/T]TTTGTATATATATAT | 93664 |
rs140730396 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122375519 | AGTGCTGGGAAAAGT[A/G]GATGTACACATACAA | 93664 |
rs140731345 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122781779 | GAAAATCTGATTTGA[G/T]TAACCAATTTATCCC | 93664 |
rs140732855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122467774 | ACCAAGACGTATAAC[C/T]ACACATATCAACCTA | 93664 |
rs140756074 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122390031 | CACCCTGGCCTCAGC[A/G]TCAAAGCTCTATCAC | 93664 |
rs140757848 | in-del | -/TG | 0.0614824 | 0.164198 | intron-variant | CADPS2 | GRCh38.p7 | 7:122425645 | CATATACACAATATA[-/TG]TGTGTATATACACAT | 93664 |
rs140768418 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122611237 | TAGAGAACAGAAAAA[C/T]AGGAGAGAGTCCAAG | 93664 |
rs140776658 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122480298 | AGTTAGATTTTATAA[-/T]TTTTTTTTTATTTTT | 93664 |
rs140808966 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | CADPS2 | GRCh38.p7 | 7:122565180 | GACTTCACCGCTATG[A/C]AGTATAACCATGTAA | 93664 |
rs140810730 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | CADPS2 | GRCh38.p7 | 7:122681359 | TGCCAAAAAGGGCCG[C/T]GGCCACGTGCAACCT | 93664 |
rs140828948 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CADPS2 | GRCh38.p7 | 7:122438162 | CAGAGTCCCAGGAGG[C/T]ATATTAAAGCAATGA | 93664 |
rs140832381 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539396 | CTGAGCTAAATAAAT[G/T]TCTGTTCATTATAAA | 93664 |
rs140851252 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122510631 | CACATTATCAACAGA[C/G]CATCATTCTGCCGAT | 93664 |
rs140857000 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122842383 | TCCTCATGAACGCTT[G/T]CTGCCCAATTTCTGG | 93664 |
rs140859260 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122603973 | CTCTGTACAACATGG[C/G]GGATGATGGATATAG | 93664 |
rs140859573 | snp | C/G | 0.000307953 | 0.0124049 | intron-variant, synonymous-codon | CADPS2, RNF133 | GRCh38.p7 | 7:122698439 | ATGGAAAATTTCCGT[C/G]CCTTTTAAGTTACCA | 93664 |
rs140861967 | snp | C/T | 3.2956e-05 | 0.00405918 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698561 | TGGCTCCCTTCTCAG[C/T]TGCCACTTTAATTTT | 93664 |
rs140872138 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122648860 | AGAGGTAAAACCAGG[C/T]CCACAAGCAAAAGAT | 93664 |
rs140882923 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122797868 | CTGAACTTAAAAGTT[A/C]AATTAAAAAATAAAT | 93664 |
rs140886834 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122645358 | ACATGTGTGTGTATA[C/T]ATGTACATGTATACA | 93664 |
rs140893372 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122575443 | TTTCTCTTCTTTTCC[-/T]TTTTTTTTTTTTGAA | 93664 |
rs140900449 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122768333 | GAAATATGCAACAAA[A/G]TCATATATAAATCTA | 93664 |
rs140930525 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | CADPS2 | GRCh38.p7 | 7:122400413 | TTGCACTCCAGCCTG[A/G]GCAATAAGAGCGAAA | 93664 |
rs140931171 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122867672 | TGTAGCCCCCAGGAT[A/C]AGCCCAACTTCTATA | 93664 |
rs140931285 | in-del | -/C | 0.166832 | 0.235761 | intron-variant | CADPS2 | GRCh38.p7 | 7:122841824 | AAGTTTAGTACTGTA[-/C]TTTTTTTTACCCTAA | 93664 |
rs140935630 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122780530 | GTCCCATCAATAATC[C/T]GATTTAGCCCATTCT | 93664 |
rs140940304 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122762163 | GTACTCAATAGAGGC[A/G]TTGGAAGATAAAGTT | 93664 |
rs140943603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122671810 | AGAGTATTTAGCAGA[A/G]GAGTAGTGAGTAGGA | 93664 |
rs140946422 | snp | A/G | | | intron-variant, upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122622002 | GCTTAAGGAAAAACA[A/G]ACTCTGAAAACATGC | 93664 |
rs140949522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122685388 | AATCAAATTCTTCCC[A/G]AGCCCATTCTTCAAG | 93664 |
rs140972925 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | CADPS2 | GRCh38.p7 | 7:122435619 | TAGTATGGAGGCTTC[C/T]GTAAAAATAAAATAT | 93664 |
rs140989955 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122345258 | AGCCTCTCGAGTAGC[C/T]GGGATTACAGGCATC | 93664 |
rs140999012 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122761330 | GCCAATACTCATCTC[G/T]GAGGAATCAAACTAA | 93664 |
rs140999095 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122718122 | AGGCATGAGCCACCA[C/T]GCCTGGCCCCCTCAT | 93664 |
rs140999648 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122851299 | CACTGAGGAGTCCTT[A/G]AGCTTAAAGTCACTC | 93664 |
rs141009815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122733907 | GATCACATCACTGCA[C/T]TCTAGTCGGGGTGAC | 93664 |
rs141010689 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122550647 | TTAGGAAAATAATTT[C/T]ATTTAATAAAAACAG | 93664 |
rs141013633 | snp | C/T | 0.0711525 | 0.174681 | intron-variant | CADPS2 | GRCh38.p7 | 7:122658677 | ACTCATAGGTGGGAA[C/T]TGAACAATGAGAACA | 93664 |
rs141030677 | in-del | -/AG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122688769 | ATGGTTGTGGTAACG[-/AG]GGGAGTTATACACCT | 93664 |
rs141032738 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122348646 | TTGAGCTGTTTACCT[A/G]TTCTTGAAATTGTGA | 93664 |
rs141038725 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122444440 | CAGCATATAAGAGTT[C/T]CAGTTTCTCCACAAC | 93664 |
rs141042246 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122785974 | GAAATAAACCACATG[A/C]AGATCTTCAAATTAT | 93664 |
rs141044176 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122405405 | CAGTGGCTCACATGT[A/G]TAATCCCAGCACTTT | 93664 |
rs141060022 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122758124 | CTTATAATTTTTAGA[C/T]ACTATCTTGATAAAA | 93664 |
rs141070865 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122395546 | GCTCAAATAATTCAG[C/T]TCCTTTTATCAAATG | 93664 |
rs141072914 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122813954 | TATTGACTATCCATT[A/C]TAGATTCAATTCTTT | 93664 |
rs141079578 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122476873 | ACATTTCATGCAAAA[C/G]TACATTACCATGTGG | 93664 |
rs141095428 | in-del | -/GT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122620420 | AACTAAAGATGTCAG[-/GT]GTGTGTGTGTATGTG | 93664 |
rs141106093 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122322700 | TAAAAACTTTGCAAA[C/T]AATTTCAGTCTTTAA | 93664 |
rs141107663 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122389268 | AATAAAACGGGCTAG[A/G]TAGGGAAGCAATCTT | 93664 |
rs141107774 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122836541 | AGGAGACACATCTCA[C/T]GTGCAGAGACACACA | 93664 |
rs141115140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122457349 | ATCCCTTTTCCAGTA[C/T]AATAAAAAATTTCAG | 93664 |
rs141121302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554829 | CAATTTGACTCCCTA[C/T]TACAATAGCTGATGG | 93664 |
rs141128327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122635948 | TTTTTTGTTTTCCAT[C/T]TGCATGATAGATCTT | 93664 |
rs141134530 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122339707 | GTCTGGCCAACGTGG[A/G]GAAACCCTGTTTCTA | 93664 |
rs141134639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122398377 | TTTTATAGTGCTCAT[C/T]CTCTTCCAATTAGCT | 93664 |
rs141138236 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122869351 | GTGACTTGTTACATA[A/C]AAAGGAACTTCTATA | 93664 |
rs141147427 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122750410 | ACCTATATTTGCATT[C/T]GTATTGTGTCTTCTG | 93664 |
rs141148840 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | CADPS2 | GRCh38.p7 | 7:122493913 | TTCATCATTTGTACC[C/G]TTCTCTATAATCAAT | 93664 |
rs141150798 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122402798 | ACAGACTGATGCCGA[C/T]GTAAGCAAGCACTGT | 93664 |
rs141185788 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122844064 | AAGGTGAGCACAGGA[C/T]CAAACACAAGCCCCA | 93664 |
rs141186109 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122431550 | TAACTAGACAAGCTC[A/G]TCAAGGGCGGGGAGT | 93664 |
rs141188054 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122792677 | TTAGATTTGCTGATC[C/T]TTCCAATAGTGTATT | 93664 |
rs141197562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122534068 | TTATTATCCTCATTA[C/T]ATAATATTCACATCT | 93664 |
rs141197579 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122713489 | CATACACAAACTGAT[A/G]TGTGTTCACTGCCAG | 93664 |
rs141222827 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122701102 | AAGGAAACTTTAAAA[C/T]AGCATGGCTAATTCT | 93664 |
rs141223062 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122415381 | TGTGTTCCGTCTTTG[C/T]CTCTTACCAGTTACA | 93664 |
rs141230795 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122552834 | AAAGGGACTGAGTGA[A/C]AAAGGGTAGAGAAAC | 93664 |
rs141232633 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122557349 | ACACAATACAGCTCT[A/T]ATCAAGAGATCTGGG | 93664 |
rs141248907 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122842048 | GTTACCTCCTAGGCT[A/G]GAAAAGGAGAGATGA | 93664 |
rs141250831 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122382208 | AATGTATTAAATAAT[A/G]TATTTCAGGAAAATG | 93664 |
rs141252132 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122787764 | ATTCCAGGATACTTG[A/G]TATTAGCTGTTAGAG | 93664 |
rs141314879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122384751 | ACACATAATGAACAG[C/T]AGTAGATTACTCTTC | 93664 |
rs141322240 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122583673 | AAGGAGATATTGTAC[A/G]TGTGTATATACGTAT | 93664 |
rs141322503 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122634529 | TGTAAATCCATCTTT[A/G]TCATTTCTGGTTACA | 93664 |
rs141329777 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122425946 | CTTGCTTTAACTCTT[C/T]TTTCCATACTCAAGG | 93664 |
rs141336327 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122774962 | TCCTAAAATTACTTA[C/T]TTTTGCTCATTTTTT | 93664 |
rs141337315 | snp | A/C | 0.0310518 | 0.120672 | intron-variant | CADPS2 | GRCh38.p7 | 7:122608209 | GACAGAGCGAGACTC[A/C]GTCTAAAAAAAAAAA | 93664 |
rs141340387 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122582246 | CGGAGCTGTCTACAT[C/T]TTATTTTATAAATCT | 93664 |
rs141340508 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122873471 | TGATGGTTTTCAGCT[A/T]CATCCATGCCCCTGC | 93664 |
rs141342371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122695170 | GAGGTACTGTATAGA[C/T]GGAGTGAGTCATTTC | 93664 |
rs141346166 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122371190 | ACATATGAAGCATCG[G/T]CAATAAATGGTCAAA | 93664 |
rs141374044 | in-del | -/A | 0.0325976 | 0.123435 | intron-variant | CADPS2 | GRCh38.p7 | 7:122863964 | GAACCCAGAAGGCAG[-/A]GGTTGCAGTGAGCTG | 93664 |
rs141376575 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122325423 | TATGTCAGTATCTTG[C/T]CATTATTCCTTATAG | 93664 |
rs141382192 | snp | A/G | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122831807 | CCACTCTCAAATATA[A/G]CAATGAAAGACTGGT | 93664 |
rs141383523 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122459901 | AAAATTAGACAATAA[A/G]TATACAATTACATTT | 93664 |
rs141384331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122415214 | GAGCGAAAGCCTAGA[A/G]TTATCAACCATACGC | 93664 |
rs141392486 | snp | A/C/T | 0.00874735 | 0.0655527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122743906 | AGGGGGTTCCAGCTA[A/C/T]GTCTCATACATTATA | 93664 |
rs141396393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122513666 | ACATGGTTATCAATG[C/T]TTCAGTTCTCAGATG | 93664 |
rs141423301 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | CADPS2 | GRCh38.p7 | 7:122577470 | TTTGCATTTACATTC[A/G]TCTATGCCACTGCAT | 93664 |
rs141438364 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122887893 | AGGCCCCCTAGTAAT[A/G]AAAGGTCTTCAGTAA | 93664 |
rs141447201 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | CADPS2 | GRCh38.p7 | 7:122877436 | AAACAAAAGAGGTAT[A/G]GCTATTGGACAGGAC | 93664 |
rs141450773 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122342313 | CAAAAACAATGGGCA[C/T]GAATCTAGGCCAATG | 93664 |
rs141451468 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122683056 | CTTGGTTCTTGTCTG[C/G]CGTCCAGGAAGAATC | 93664 |
rs141454837 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122434194 | GTGCTGTCATAAGAG[A/G]TGACAATCAGTCCCA | 93664 |
rs141457160 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122419308 | AAGAGAGCATGCTCA[C/T]GATAAAACGCAGCTG | 93664 |
rs141457305 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122367606 | CTGGAGTGCAACGGC[A/G]TGATCTCAGTTCACT | 93664 |
rs141461155 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122519659 | ACTAAATATATTCCA[G/T]TTTCATTCATCTATG | 93664 |
rs141461455 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | CADPS2 | GRCh38.p7 | 7:122741583 | TGTGTCTATTTTTTT[A/C]AATATTACAATCTTG | 93664 |
rs141481942 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122815757 | CACTGATAGAAGAAG[C/T]TGTTTCCATTTTACT | 93664 |
rs141485817 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122576824 | GTTGCCCAGTGGCGC[A/G]ATCTCGGCTCATGAA | 93664 |
rs141488055 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122653554 | AAAAAATATACAGGC[A/G]TACATCATTTTATTG | 93664 |
rs141497596 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122630986 | CAGAAACAAGTTTCT[C/T]TTCACTGTGTCTAAA | 93664 |
rs141513963 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122864119 | GGATTATAGAACATA[A/G]AACAATCAACCTCCA | 93664 |
rs141515025 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122359838 | TAGAAAAGTCCAGGG[C/T]CTTCTCATTTAAAAT | 93664 |
rs141526496 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122857628 | TTAAGATTTCCTATT[C/G]AAACAAGTTTCCCAA | 93664 |
rs141527816 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122368388 | CCCTCCCTGGTCTTG[A/C]TGAGTTCTGCATGGT | 93664 |
rs141531469 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122584149 | AAGTTGAAAAGTGCT[A/G]TATTTTTATTATCTG | 93664 |
rs141535545 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122618133 | GTTTTTCTAGTATTG[C/T]TTGAACATTTAACAT | 93664 |
rs141536031 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122408716 | ACTGGTGTAAGCCAC[A/G]GCACCTGGCTTCAAA | 93664 |
rs141537122 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122457970 | ACCCCATCTCCAACT[C/T]ATCAGGTAAGTTTGT | 93664 |
rs141556459 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122349212 | CGGTTAAACTTCAAC[A/G]GCTGTGGATTCAGAT | 93664 |
rs141556594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122687274 | ATTATGTTGAGATCA[C/T]GTAAGGTATCATTCA | 93664 |
rs141586300 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122619630 | AGACTCAGTCTCCAA[A/C]CAAATAAATAAATAA | 93664 |
rs141587996 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122819231 | GGCCAAGGAATGCCC[A/G]CAGCCCAGGATTCCT | 93664 |
rs141589516 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122771813 | AAAAGAGAAACTGTG[G/T]GTACCTGACAACAGT | 93664 |
rs141589558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122828742 | AAGTTCTTTGCCTTC[C/T]TTCATCTGAGACTGT | 93664 |
rs141590157 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122731209 | AAAACTATACATCCT[C/T]TCTGAAAAGTTGTGA | 93664 |
rs141595558 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | CADPS2 | GRCh38.p7 | 7:122691590 | AGAGGTTCGCATAAC[A/G]TCATCAACAAGATCA | 93664 |
rs141599691 | snp | C/T | 0.00232311 | 0.0340023 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698050 | ATGGGGCATGTCCCA[C/T]GGGGTAAAATCCAGG | 93664 |
rs141605365 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122594452 | TCCCTTTCCCTTCAA[A/T]GAGCTAGTTCTCATT | 93664 |
rs141610137 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122507853 | GTTTTTGCTATGGAA[C/T]AGCAATCTTTTCTGC | 93664 |
rs141611253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122455991 | TACAGGAAAGAGCCA[C/T]CATGCCCAGCTTGGA | 93664 |
rs141614888 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122729199 | AGATGATAGGATTTC[A/G]TTCTTTTTTTTACGG | 93664 |
rs141621216 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554470 | GCCTGCTATACTGGT[C/T]CTCTCACTAAACTGA | 93664 |
rs141621849 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122829290 | TTATACTACTGGCAC[A/T]AATAAATTCAAACAT | 93664 |
rs141622374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122600882 | TGCTCACATATAAAA[C/T]AAATAACTGGATGTG | 93664 |
rs141627683 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122356895 | GTATATTTTTCAGCA[C/T]CAGCCATTTCTCCAA | 93664 |
rs141633239 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122448721 | GAGGCATCCCGTGCA[A/C]AGAATTTCTCTGGCC | 93664 |
rs141671685 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122862821 | AAATAAATACATGAT[C/G]CTAACTGGAATAGAA | 93664 |
rs141676037 | snp | A/G | 0.0607341 | 0.163335 | intron-variant | CADPS2 | GRCh38.p7 | 7:122404854 | CATATGGCCGGGCGC[A/G]GTGGCTCATGCCTGT | 93664 |
rs141676886 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122361742 | TACTTGCCATCCTTC[A/C]ACTTTTTCTACATCT | 93664 |
rs141677644 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122639913 | ATCTAGTCTCTGATC[C/T]TCCAAGTGTGTATCT | 93664 |
rs141678992 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122453980 | TTGGACTTGCCTTTA[C/T]ACATCCTTATTTTAG | 93664 |
rs141683283 | snp | A/T | 0.00279329 | 0.0372672 | intron-variant | CADPS2 | GRCh38.p7 | 7:122514890 | TTCAAAACTACACAC[A/T]TAGTTAATGATTTGG | 93664 |
rs141693788 | in-del | -/GAGGTTGAGGTGGGCGGATCAACT | 0.206642 | 0.246211 | intron-variant | CADPS2 | GRCh38.p7 | 7:122827416 | ATCCCAGCACTTTGG[-/GAGGTTGAGGTGGGCGGATCAACT]GAGGTTGGGAGTTTG | 93664 |
rs141697772 | snp | A/G | 0.00281599 | 0.0374175 | intron-variant, stop-gained | CADPS2, RNF133 | GRCh38.p7 | 7:122698201 | CCTCTTTTACTACTC[A/G]AAGTTGGAGTTGTCC | 93664 |
rs141700906 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | CADPS2 | GRCh38.p7 | 7:122464373 | TAAACAAATGGTTAA[A/G]TAAATAAATTGGAAA | 93664 |
rs141706978 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122503396 | TTAGATTCTATTGAA[A/C]ACGTTACTGAATGAT | 93664 |
rs141712032 | in-del | -/TTTA | 0.339429 | 0.233457 | intron-variant | CADPS2 | GRCh38.p7 | 7:122757156 | AAGTTAGGTATAGTT[-/TTTA]TTTATTTATTTTGAG | 93664 |
rs141729658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122746981 | CGTCTGCCTCACTCA[C/T]TTCTCTGAGAGTGAA | 93664 |
rs141736994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122756582 | TATGTCATAATCAGC[C/T]ATTATTTTAAAAATG | 93664 |
rs141737919 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122644491 | ATTTATGAGCTTTAT[A/G]TATTTCACCTTACCC | 93664 |
rs141748547 | in-del | -/AG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122719504 | GCATGCTGGGCAGAA[-/AG]AGAGAGAGAAAAGGC | 93664 |
rs141753934 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | CADPS2 | GRCh38.p7 | 7:122452762 | ATCATTCCAATGTAC[C/T]AATTTTAATGGTTAT | 93664 |
rs141755648 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122880267 | ATATATACTTTCTGT[C/T]GCTAATGTGGTGATT | 93664 |
rs141758250 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122718404 | GTAGGAGAGAAGTAG[A/C]AAGAGGGAGGAAGAA | 93664 |
rs141760468 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122605185 | AGGAAATTGCAGGAC[A/G]GGAAGTTGCTCTAGG | 93664 |
rs141761332 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122503920 | TTTGCAGGAAAACAA[A/C]GCAGAGGAAAGAGAC | 93664 |
rs141768713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122755751 | AAAAAAGGGAAACTG[A/G]TAAGATATTTCATAA | 93664 |
rs141768842 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122426600 | TACTTATAAACCCTG[C/T]TGATAAATACAGAGG | 93664 |
rs141773311 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122596511 | TGGCCTTCGTGACTC[A/G]GGCTTGTGTTAAAAG | 93664 |
rs141774146 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, nc-transcript-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122530390 | TAAAAACAAATTTTA[A/G]AAAGTGAGTAAAATG | 93664 |
rs141776674 | in-del | -/AACTT | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122743137 | AAACTAAATTGCAGA[-/AACTT]AACTAAAACATAAAT | 93664 |
rs141779221 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122562546 | TTGAACTTCTGACTT[C/G]AGAACTATAAGATAA | 93664 |
rs141789761 | in-del | -/C | 0.0622301 | 0.165053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122484911 | ATGACGTGCTCATAT[-/C]CATGACTGTTTCATG | 93664 |
rs141793897 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | CADPS2 | GRCh38.p7 | 7:122838461 | AAGAAAGAAAGGGTA[C/T]TCAATTAGGAAAAGG | 93664 |
rs141800604 | in-del | -/AATA/AATAAATA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122592988 | ACTTGAAGTAAAATG[-/AATA/AATAAATA]AATAAATAAATAAAT | 93664 |
rs141802098 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122378109 | TATTACGAAACTCTT[C/T]ATTTATCATTAATAG | 93664 |
rs141810301 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122412779 | TCAGCCCTTCTACTG[A/G]TATTCTCCGCACTCC | 93664 |
rs141814250 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122508942 | TTTTATCCTACACTG[A/G]GTATGTTCTGGGTTT | 93664 |
rs141814915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122719034 | TTTTGAGGAAGTGAG[C/T]AAAGGAAAAGCCACA | 93664 |
rs141846460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122535376 | GAACTAAATAAGAAT[A/G]TTATTTAATGTGATA | 93664 |
rs141873169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122392119 | CTCTCATGATTATTC[C/T]TTCTAGTTGATTTCA | 93664 |
rs141884701 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122714903 | ACACTATCAGAATCT[C/T]GTTTTATCAATTAGA | 93664 |
rs141899307 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122851440 | TTCAGCTATCAATTA[C/T]GCTTCCCACAGCAGG | 93664 |
rs141903942 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122672526 | CTCTCCAATATCATC[A/C/G]TCTTTTAAAGGTTAA | 93664 |
rs141906082 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122600390 | CATGAAACAGTCATA[A/G]ATATGCCCAAGAAAA | 93664 |
rs141919264 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122588842 | GTAGATGGGCACCTC[C/T]CCCAAACTCATTATG | 93664 |
rs141946039 | snp | C/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122444067 | AAGTAAGAGGAAATG[C/T]ACAGTATTTACTTTT | 93664 |
rs141948626 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | CADPS2 | GRCh38.p7 | 7:122338175 | GCTGAAGTGGGCAGA[C/T]TGCCCGAGCTCAGGA | 93664 |
rs141948948 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122430443 | AATTGATTCTTCTTT[C/T]AAAATAATATCTAAT | 93664 |
rs141951997 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122391452 | ATAGTGTTCTTGGCT[A/G]AAATCAAGCGTTAAA | 93664 |
rs141952550 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122541146 | AATAGAAAAAGCAGC[A/C]CTTTTAACTTTCATA | 93664 |
rs141977527 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122726281 | ACTTTGATAATCAAT[A/G]CAAAATTAAATTTTA | 93664 |
rs141984804 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | CADPS2 | GRCh38.p7 | 7:122651706 | TAAATCTGGGTGAGT[C/T]GCTTTCTTCAGTTAA | 93664 |
rs141995407 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122795873 | AGGGCTGTCAGGCAA[A/G]AGAAAGCAATATAGG | 93664 |
rs141997119 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122845140 | TGTCATCAGTCAGAA[A/G]CAGGATAATAAACAT | 93664 |
rs141999584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122716030 | TGTTCTCATCACAAA[A/G]AAAGTATGTGAGGTG | 93664 |
rs142018426 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122859202 | TGAAAGTTTATATTA[G/T]GTTAAAGAAAAATAT | 93664 |
rs142018886 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122536998 | GCACATAGAGGAGAA[C/G]ACCACATACTGAGAC | 93664 |
rs142020493 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122770844 | GCACTCAAGCAGGTT[C/G]CAGACAACTAGGACA | 93664 |
rs142025704 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122807712 | CTGACTTGCAAATGG[A/G]TACCCTCTTGCTATA | 93664 |
rs142029135 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122622710 | TTAAAATGACCACCA[A/G]TGCACAGAACCGGCT | 93664 |
rs142030042 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122749584 | TTCAAGTAAATTAAA[C/T]TATATTGATTAGTTA | 93664 |
rs142036303 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122576126 | GTGACAGTTTCTCAC[C/T]TTTCTTTTTTATGAC | 93664 |
rs142057708 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122843208 | GCTAGACAAAAGCAT[G/T]TACTCAATCACACAT | 93664 |
rs142075016 | in-del | -/AGG | 0.121369 | 0.214369 | intron-variant | CADPS2 | GRCh38.p7 | 7:122853210 | AAATGAGATACTAGC[-/AGG]AGATCAGATAAACGA | 93664 |
rs142076531 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122623849 | CGTATCTGAAAGTTC[C/T]GATATACTAACGCTT | 93664 |
rs142077275 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122384992 | TAAAATAAGAACAAA[C/T]GGATAAACCCAGTAT | 93664 |
rs142082265 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122482203 | AGTGAAGGAGGATGG[C/T]GATTAAAAAAAAATA | 93664 |
rs142088358 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122884367 | GCTGATTAGGAAGTA[C/T]GGGATTCATACAGGA | 93664 |
rs142090464 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122330544 | AACTATCATACCTGG[A/G]TTCCATAAAACCAGA | 93664 |
rs142091007 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | CADPS2 | GRCh38.p7 | 7:122724209 | AAAAATAAAAATAAA[A/G]TAAAAATAAATCTGT | 93664 |
rs142092292 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122424637 | AGAACCCACAAGCAA[A/C]AATTAGTATTTGGTT | 93664 |
rs142098920 | in-del | -/ATAC | 0.0360663 | 0.129354 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122540974 | GTCTGAACACTATAA[-/ATAC]ATAGAGAGTACTTAA | 93664 |
rs142107244 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | CADPS2 | GRCh38.p7 | 7:122489641 | ATCTACAACAAAAAA[A/G]TAGACCTATTATCCT | 93664 |
rs142120344 | snp | A/C | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122855125 | GGTGGGAGAAGAACA[A/C]TGATGGGACAAAAAG | 93664 |
rs142132037 | snp | A/C | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122777221 | TAAAATAGCTTATTT[A/C]TCTCATAAAAGGAAC | 93664 |
rs142136693 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122338347 | TACAGTGAGCTGAGA[C/T]TGCGCCACTGCACTC | 93664 |
rs142167604 | snp | C/G | 0.000350007 | 0.0132243 | missense | CADPS2 | GRCh38.p7 | 7:122407620 | TGAGCCTCTAGTGCA[C/G]TGTCCATATCCACTG | 93664 |
rs142169271 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122479476 | TAGATCAGCCTGAAT[A/G]GTATGTCCATGTTTT | 93664 |
rs142171999 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122732974 | ACAGCTAAAGGATTG[C/T]AAACATAATAAATGA | 93664 |
rs142174263 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122686251 | TGTGATAGTGGTAGC[A/G]GATAGAGAAACCAGT | 93664 |
rs142179620 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122542830 | CATAAGAGGAGTTAA[G/T]CCCTTTCTATTCTTA | 93664 |
rs142180379 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122572537 | GTTATTTTGGCAAAC[A/C]CTCCAAAAATTTTTT | 93664 |
rs142180509 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122624587 | CCTAACTAAATCGTT[G/T]AAGTGTTTAAATGTT | 93664 |
rs142194158 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122728279 | GTAAGGTAATTACAT[A/G]AAATTTTAAAAGCCT | 93664 |
rs142195547 | in-del | -/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122369053 | GTACCCTTTCCTTGG[-/T]AAGATTTAATGCTCC | 93664 |
rs142206327 | in-del | -/GTGTGTGT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122527618 | AGAGAGAGAGAGAGA[-/GTGTGTGT]GTGTGTGTGTGTGTG | 93664 |
rs142221746 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122861716 | CAAGTTTCAGGTGAC[A/G]GATATACTAATTGCT | 93664 |
rs142225798 | in-del | -/TTAAG | 0.0629771 | 0.165899 | intron-variant | CADPS2 | GRCh38.p7 | 7:122383536 | GATTTCAATTCATTC[-/TTAAG]TTAAGTTTCTCCACA | 93664 |
rs142227960 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122774628 | AATTCTGCAGTCTAA[C/T]TTCACATCTGATATG | 93664 |
rs142236879 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122665895 | CAACACAAATTAATT[C/G]TTAAGTGACAGGTAT | 93664 |
rs142258532 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122871593 | GCTAGATTCAGCATA[C/T]AAAATACGGTTTAGG | 93664 |
rs142270601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122674854 | TCTCCTGAATAATGC[C/T]AAATAAAATATTGTC | 93664 |
rs142280585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122404752 | TGAATAATGCCTCAT[C/T]TTAAAATAACCCCCA | 93664 |
rs142284163 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122656866 | GCTTCTGGTGTTTTA[C/G]ACATGAAGTCCTTGC | 93664 |
rs142298513 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122806583 | TATTAACAACAACCC[A/G]AATGATTTTATCTTT | 93664 |
rs142306398 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122694891 | ACAGTAGCAGCATGT[A/C]AAAATTTCTCTGCTT | 93664 |
rs142312084 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122690063 | AGCTGCTGCTGGAAG[A/G]ACAGTGCCGATCCAA | 93664 |
rs142315113 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122620623 | ACACAATTTTAAATG[C/T]ATGACTTTTCTTCTT | 93664 |
rs142333085 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122365162 | TATATACAAGTTAGT[A/C]CTAGGTGTGAACCTG | 93664 |
rs142340390 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | CADPS2 | GRCh38.p7 | 7:122455758 | GTCACCCAGGCTGGA[A/G]TGCAGTGGCACAATT | 93664 |
rs142348044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122410962 | AGATTAAATAACTTG[C/T]CCAAAGTCATACAGT | 93664 |
rs142355131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122825961 | AGGGTGGTGTAAGAA[C/T]GCCAAGTAGCAAGCT | 93664 |
rs142357706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122740257 | AGTTGGAAATTTATG[C/T]CCACACAAATACCTG | 93664 |
rs142383162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122558714 | CACACAGAAATGTTT[A/G]GAGTGATATGGGGTT | 93664 |
rs142384198 | snp | A/C | 0.030665 | 0.119967 | intron-variant | CADPS2 | GRCh38.p7 | 7:122877783 | ATTAACAACTAGAAA[A/C]GATAGCGTCTAATCA | 93664 |
rs142394849 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122770054 | AATAGGGAGCCTGAC[A/C]CATAGAAAGGTTAAG | 93664 |
rs142396827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122825852 | ATCTAACTAATTCAA[A/G]TTTGCCCACGTCCCC | 93664 |
rs142397131 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122506015 | GTAATCTGGAGAAAT[C/T]GTACTCAGACCTGTA | 93664 |
rs142399329 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122680390 | CTAAATCCCTTATGA[C/T]TAATCTAAACCCCTC | 93664 |
rs142403227 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122690524 | ATCTGCAATGAGGGG[C/T]TTGGAGGGTCCATGG | 93664 |
rs142407375 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122599501 | TTACAGCTAGAAATA[C/T]CACATACTGAGTTGA | 93664 |
rs142412243 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122731549 | ATGATGTTTCCTAAA[C/T]TGAAAAATAGACCAA | 93664 |
rs142421143 | in-del | -/GAGT | 0.0225045 | 0.103662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122574429 | CCAGCCTGGGTGATA[-/GAGT]GAGACCCTGTCTTAA | 93664 |
rs142428163 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122813463 | ACTCATCATTTCAAA[C/T]TGTTTATTACCATCA | 93664 |
rs142429516 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122459407 | TTGCTAGGTTAAATG[C/T]ACGATATTTTCAAGT | 93664 |
rs142454421 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122359255 | AAGAGAGATTAGAAC[A/G]AGGATTAATGGGTAA | 93664 |
rs142456914 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122610182 | CACTGGGGGCTTATT[A/G]TAATACTTCCTCTCA | 93664 |
rs142464527 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | CADPS2 | GRCh38.p7 | 7:122822294 | AATTCATCCAAAACC[A/G]TATCCAGGCCATCAC | 93664 |
rs142465282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122864610 | ATAAGGAAAATGACC[A/G]TCAAGTAGGCAATTA | 93664 |
rs142467642 | in-del | -/G | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122584673 | CCTTTCTTCCATTCC[-/G]GGCAAGCATTTGTGA | 93664 |
rs142474246 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122327992 | GCTCCTAAGTCAAAG[C/T]ATTTTCAAGACACAC | 93664 |
rs142487114 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122638220 | TAGACAAGACTATAC[C/G]CTTTCTGGAAAGCCC | 93664 |
rs142491919 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122406080 | ATGCCTCCCTTACTA[C/G]AACAGAGGTTTTTAA | 93664 |
rs142503237 | in-del | -/T | 0.409721 | 0.192325 | intron-variant | CADPS2 | GRCh38.p7 | 7:122367376 | AAATCCTTTTTTTTT[-/T]GGCAATAATTGAGAA | 93664 |
rs142515876 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122602009 | AACTTACTGACAAAA[A/C]ATGTATAAATAAAAG | 93664 |
rs142522774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122580729 | TTTCATGGGGAAAGT[A/G]GAAAAGATAAGAGAG | 93664 |
rs142534338 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122767872 | GAAAATTTGAGCTTC[C/T]AGAATTCTGGGATGC | 93664 |
rs142538989 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | CADPS2 | GRCh38.p7 | 7:122753996 | TTTCATTTTGGCTAA[C/T]AGGATGTGGTGCAGA | 93664 |
rs142541167 | snp | C/G | 0.0263992 | 0.111815 | intron-variant | CADPS2 | GRCh38.p7 | 7:122501047 | ATCACTTGAGGCTAG[C/G]AGTTCAAGACTAGCG | 93664 |
rs142547590 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122344991 | AACTGATGGCAAGAA[C/T]GGATTTCAGTAAATA | 93664 |
rs142549298 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122676533 | ACAATAAGCTTATGT[A/T]CAAGCAGCAGTTGGA | 93664 |
rs142551042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122804153 | AAGTCTAGAGGTGAA[A/G]CTTTAATCCTAGCCC | 93664 |
rs142555103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122437867 | AAATGCATCAGTACA[C/T]TGCAAGCAATTAAAA | 93664 |
rs142560986 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122719419 | TAAAGAAGGCAGGGG[G/T]CCAAGTTCACACCAG | 93664 |
rs142581909 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122553435 | TAAAGATGCATAATG[C/T]TGTTTATCCAAATCA | 93664 |
rs142597737 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122634262 | TTGTACATCTGGTAG[A/T]ATTCAGCTATAAATG | 93664 |
rs142619835 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122362119 | AAACAAACAAACAAA[A/C]AAAATGAACAGATAA | 93664 |
rs142623225 | snp | C/G/T | 0.00478244 | 0.0486902 | intron-variant | CADPS2 | GRCh38.p7 | 7:122333407 | AGAGTGTCCTAAGGA[C/G/T]GGGAGTAGACAGCTA | 93664 |
rs142624375 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | CADPS2 | GRCh38.p7 | 7:122641962 | AGCATCAGGATGGAT[G/T]TGCAAAGATAGAAAT | 93664 |
rs142627863 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122493570 | AAAATGGTTACTAGT[A/G]CACAGTGTGGGTGAC | 93664 |
rs142630831 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122586399 | TAGATATAACTTGTG[A/C]CCACTTTTGACCTGT | 93664 |
rs142637492 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122677673 | AACAATAAAAACCCA[A/G]AAAGCATACAGAAGT | 93664 |
rs142645914 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122689859 | CAATGGGGGCACCAC[A/G]TGTTCTCCCATTAGA | 93664 |
rs142671210 | in-del | -/CAATC | 0.0130921 | 0.0798413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122375194 | AAGTAACAGAAAAAG[-/CAATC]CAATCCTAAAATTCA | 93664 |
rs142674759 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | CADPS2 | GRCh38.p7 | 7:122625353 | CCGCATCTAGCCCAA[C/T]TAATTTTGTTTGTCA | 93664 |
rs142695415 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122702560 | TCCAGAGGAGAATGA[G/T]TCCCGAACACTCCAC | 93664 |
rs142704472 | snp | G/T | 0.0345262 | 0.126772 | intron-variant | CADPS2 | GRCh38.p7 | 7:122821167 | CTCTCTGATCCACCT[G/T]ACATTCACCCCATTT | 93664 |
rs142716487 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122703238 | TTTCTAGCTGTAAGG[C/T]AAAGGCAAAGATAAA | 93664 |
rs142736274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122664648 | TCCTCCATAAGCCAT[A/G]TAAGACTGCTTTTAT | 93664 |
rs142754440 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122340730 | GAAACATCACAGTAG[G/T]CATTAAAAATGGAAT | 93664 |
rs142757635 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122598516 | CCACAGAAAGTGATT[A/C]GTACAATGTCACTTA | 93664 |
rs142765683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122831711 | CAATTTTGCCAAAAA[C/T]TGTAGATCCCTTTTT | 93664 |
rs142768538 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | CADPS2 | GRCh38.p7 | 7:122433018 | TCCTTCTGTCACCCA[C/T]GCTGGATTGCAGTGG | 93664 |
rs142770271 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122660367 | AGAATCACCAAAATT[C/T]TGTTTCGTTTTTTAA | 93664 |
rs142770306 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | CADPS2 | GRCh38.p7 | 7:122709715 | ATATACACCATGGAA[C/G]ACTATGCAGCCATAA | 93664 |
rs142794466 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122874854 | CTGAAACTGGACCCC[C/T]TCCTTATACCTTATA | 93664 |
rs142800889 | in-del | -/GA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122732442 | AGCAATCATAAAGCT[-/GA]GAGAGAAAAATAATA | 93664 |
rs142801882 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122373411 | TAATTTTTTTGTGTA[C/T]GTGTGCTAACATTTA | 93664 |
rs142813569 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122452251 | CTAAAATTTTGAACA[G/T]ATAAATCTTAACTGT | 93664 |
rs142821236 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122751521 | TTGCAGAATGTAAAT[G/T]ATGACCTTTTGTCAA | 93664 |
rs142834864 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | CADPS2 | GRCh38.p7 | 7:122486652 | CATAAACTTAGTTCG[C/T]AAAGCAGAGGTAAAG | 93664 |
rs142839198 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122578808 | ATAGTAAACAGACTC[C/T]TTATGTGAAATGATG | 93664 |
rs142842571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122843421 | CAACTACTTTGACCT[A/G]TGGGGTGTCACTGTC | 93664 |
rs142844108 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | CADPS2 | GRCh38.p7 | 7:122833382 | TTGAGATGGAGTCTC[A/G]CTCTGTTGCCCGGGC | 93664 |
rs142844223 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122574338 | ATGGCCTCAGATACT[C/T]TGGAAGCTGAGGTAG | 93664 |
rs142861196 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122417466 | ATGTTGTTGGCTGTA[A/C/G]GAAGTAGAAGGCAGT | 93664 |
rs142862670 | in-del | -/A | 0.0352966 | 0.128072 | intron-variant | CADPS2 | GRCh38.p7 | 7:122826627 | ACAGAATTTATGAAG[-/A]AAAAAAAAATAAGAA | 93664 |
rs142869791 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122516140 | TTGGAACCAAGGTAA[A/G]CATTTAAATGATGAT | 93664 |
rs142873858 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122573180 | TTGGAAGTGTTTAAA[A/T]TACTCCCTCCTTGGC | 93664 |
rs142877210 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122780071 | TCCATAATTTTAGGA[C/G]AAAAGAGGTATGTAG | 93664 |
rs142882805 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122333737 | GCACAATGTAGTTCA[C/T]GTCTCCCTCAATCAG | 93664 |
rs142885527 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CADPS2 | GRCh38.p7 | 7:122671693 | TACAGTGAGAAAGAA[C/T]CCCTGGATAAGCAAA | 93664 |
rs142892736 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122374137 | ACCACATTAATAGAA[C/T]GAAGGATAAAAATCA | 93664 |
rs142893720 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | CADPS2 | GRCh38.p7 | 7:122466441 | TCCAGCAACATGGGG[G/T]TGGTAGGCGGGGAGG | 93664 |
rs142896103 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122428084 | TAGCTAGTGGATTGA[C/T]GGAGTGGAGCAGTGG | 93664 |
rs142906274 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122605198 | ACGGGAAGTTGCTCT[A/G]GGTGAGTCAGTGAGT | 93664 |
rs142913995 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122623706 | TCTGGTTTTAACACC[C/T]AACTTGTTTGCTTAT | 93664 |
rs142927164 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122421514 | TATGCATTCATTTCT[C/T]CTTTGGTTTTTAAAC | 93664 |
rs142930079 | in-del | -/CACCT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122725903 | AGGACGCCTGGATGA[-/CACCT]CACAGATAGCAGATA | 93664 |
rs142942403 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122884314 | AGAATTGAGAAGAGG[A/C]CACGGGTGACTGCCT | 93664 |
rs142948275 | snp | A/T | 0.030278 | 0.119257 | intron-variant | CADPS2 | GRCh38.p7 | 7:122761721 | AAATGTAGGCCAGGC[A/T]TGGTGGCTCACACCT | 93664 |
rs142952062 | snp | A/G | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122735931 | TACAAGGTGAAATCT[A/G]AGGTCCTATAGATGT | 93664 |
rs142957986 | in-del | -/CCTGACTAATATAC | 0.0119091 | 0.0762411 | intron-variant | CADPS2 | GRCh38.p7 | 7:122853628 | TTTTTCTGACTAGAT[-/CCTGACTAATATAC]CCTTACATCAAGAGT | 93664 |
rs142962531 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122429798 | GCCACATAAAACTTT[C/T]ATCAGAGAAAACTGT | 93664 |
rs142977640 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122574912 | ATCTTTACGATGGAG[A/G]GAACTGGCAGATGCC | 93664 |
rs142979446 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122626725 | ATGTATCCCAAGTAG[C/G]TAAGACTGCACCTGG | 93664 |
rs142990180 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122770725 | GCTCAGGATCTAAAG[A/G]TGCCTGCATTATAGA | 93664 |
rs142994356 | snp | C/T | 0.211516 | 0.24702 | intron-variant | CADPS2 | GRCh38.p7 | 7:122723555 | gaggatgtggagaaa[C/T]aggaacactttcaca | 93664 |
rs142995736 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122381657 | AGTCAGTGGACACTA[C/G]GAACCATTAAATTCT | 93664 |
rs143005562 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122469171 | TGCCTCCCAGGCAGC[A/C]GCAGTAGCTCCTTGT | 93664 |
rs143005851 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | CADPS2 | GRCh38.p7 | 7:122819439 | TAGACCATCACGGAC[A/G]CCAAGCTTCGGGTAA | 93664 |
rs143005909 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122868861 | AGATAGAACATATTA[A/C]AAACTACTAAACAGA | 93664 |
rs143010788 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122801507 | TCCTTCATTTAATAA[A/T]AAATATCTAGCACAA | 93664 |
rs143013289 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122600589 | CAGCAGAAATCAAGA[A/C]CCCTGCTCTAAGCAA | 93664 |
rs143016464 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122718780 | AGAGGACCAAGTTGT[C/G]AGCTCAAGACTCTAA | 93664 |
rs143017876 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122361088 | ACAAACAATTCCTGA[A/G]TCAATTTCTTCCATC | 93664 |
rs143024482 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122614316 | TTCTGTTACACATAA[A/C]CCTCTGTATCTCCCT | 93664 |
rs143024731 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122520344 | GGTTGAATGTGTGTG[-/T]TTTTTTTTTAAGTAG | 93664 |
rs143029781 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122696779 | AAATTTTCTGTTATT[C/T]TGTATAATTGGGAAA | 93664 |
rs143047291 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122844375 | ATACTCAATGTTATG[A/T]TAAAAATCAGGATTC | 93664 |
rs143048186 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122852173 | AAATTATTGCTGTCA[C/T]ATTAAATATAATTAA | 93664 |
rs143073583 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122400841 | TGAAAGAGAATAACA[C/T]GCAGGTGTCAGCCTT | 93664 |
rs143076994 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122526848 | TACTCCCCACACAAG[A/T]CTGCAAACTCCATGA | 93664 |
rs143081032 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122616642 | ATGAATCAAAATCAG[G/T]ACTTAACTGAAAACA | 93664 |
rs143088395 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122673146 | CGCTGTGAGTGTTAC[A/C]GCTCTTAAAGGCGGT | 93664 |
rs143094724 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122691433 | ACTATTTGTGGTCAC[A/G]TGCACATTCAGTTTA | 93664 |
rs143102522 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122376060 | CATCTGTTTGGATGG[C/T]TATTATCAACAACCC | 93664 |
rs143107580 | snp | C/T | 1.65081e-05 | 0.00287293 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122697979 | CTTGCAAAGGTTCTG[C/T]TCCATTTTCAACAAC | 93664 |
rs143139841 | snp | C/T | 0.312837 | 0.241974 | intron-variant | CADPS2 | GRCh38.p7 | 7:122820174 | GTTCTAGATCTCAAA[C/T]ATGCTTTCTTTACTA | 93664 |
rs143141168 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122726185 | CAATGACAAAAATGA[A/G]TATTCTTGACAACTG | 93664 |
rs143142006 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122762255 | AAATAAATCAGAGAA[C/G]AAGCTGGGCGGCAGT | 93664 |
rs143146389 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122851342 | GAATGGGTCTAGCTG[A/T]CCCTTCTGTGCCCAA | 93664 |
rs143151492 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122337847 | GCTTGACTATGACTA[-/T]CTTAAAAGAGGTCAA | 93664 |
rs143151574 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122764645 | GAGTGCTACTTTAGA[C/T]AGAATGGTGAAAAAG | 93664 |
rs143151970 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122650657 | TTTAGAATATTCTTA[C/T]GTAACTCTTCCACAT | 93664 |
rs143153092 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122685492 | CACTTACTATCCTAC[C/T]GGCTCTCCTTAACAC | 93664 |
rs143158585 | in-del | -/AAC | 0.331179 | 0.236453 | intron-variant | CADPS2 | GRCh38.p7 | 7:122782364 | CCTGCTCATTACTGA[-/AAC]AACACCAGTAGCAAA | 93664 |
rs143167320 | in-del | -/TC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122625756 | CTTGAACGCAATCAA[-/TC]TCTCTCTCTCTCTCT | 93664 |
rs143173758 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | CADPS2 | GRCh38.p7 | 7:122398949 | AGACTAGGAAACACA[C/T]TGGATTCTATTGTCC | 93664 |
rs143180532 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122432801 | TCAAGAGACTACAAG[A/G]GACTACAGTGTCAAA | 93664 |
rs143184505 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122534695 | AGATTAACAGTAATG[C/T]ACATCAATGGAAATG | 93664 |
rs143197313 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122571524 | GTGAAGACTCAGGCC[A/T]ACTTCTCAGAGAATG | 93664 |
rs143215592 | snp | A/T | 0.0248432 | 0.108648 | intron-variant | CADPS2 | GRCh38.p7 | 7:122396755 | TCTACCCTGGACAGG[A/T]TTCCACTGTGGTTCT | 93664 |
rs143226085 | in-del | -/TTAT | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122760313 | TGTATATTTAGGTAA[-/TTAT]TTATAGATATAGTCA | 93664 |
rs143230116 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122647913 | AATATATAATGTTCT[C/T]TGTTACTGGCTGATT | 93664 |
rs143231772 | in-del | -/T | 0.117886 | 0.21224 | intron-variant | CADPS2 | GRCh38.p7 | 7:122451713 | AGATTATAATAAATA[-/T]TTTCCAGATCTACCG | 93664 |
rs143233919 | in-del | -/ACACACAC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122774270 | GACATAGATAGATAT[-/ACACACAC]ACACACACACACACA | 93664 |
rs143241999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122357060 | ATGCATATACATATA[C/T]CTAAAAATACTGTTA | 93664 |
rs143244171 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | CADPS2 | GRCh38.p7 | 7:122449537 | ACGTTGCCTAGGCTG[G/T]TCTTGAACTCCTGGG | 93664 |
rs143259986 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122729909 | GTATGATGTAAATCA[C/T]TGTTATCAGTGATTT | 93664 |
rs143264305 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122695379 | TGCATCACTAGGTAC[A/C]AGAGAAAATGGTATA | 93664 |
rs143273880 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122766427 | GAAATATTTTATACC[A/G]ATAAGAATATTTCTA | 93664 |
rs143281453 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122396578 | TCCAAGACCTGTCTA[C/G]AAGTTACTTCTCCAG | 93664 |
rs143287336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122767546 | TAAAATGAAAAGTCA[A/G]TAGTTGAGAGGCATT | 93664 |
rs143287377 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122857208 | AACGATAATGATAAG[C/G]ATGAACTGCTCAGCA | 93664 |
rs143288048 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122444591 | GCATCTTTCCATATG[A/C]CTTTTTGTATAATAT | 93664 |
rs143297335 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122689577 | CTCTAGTCATGTAGG[C/T]GACCAGGCAATGTGG | 93664 |
rs143319129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122462433 | CCAATAAAAAGTTTA[C/T]AGAACATGAGCCAAA | 93664 |
rs143323656 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122499470 | TGACCTACGTATTTA[A/C]AAACATGGGCACTAT | 93664 |
rs143325834 | in-del | -/T | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122779901 | CTAGGTAGCCATTCC[-/T]TGCCTGTGTTGAATC | 93664 |
rs143327251 | snp | C/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122792029 | GCTTTCCCCTGAATA[C/T]AGTAATGGAAGGAAC | 93664 |
rs143333315 | snp | A/C/G | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122590106 | AATATGAAAATCTAC[A/C/G]CTAAAATTCATAAGG | 93664 |
rs143333580 | in-del | -/GT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122433148 | TTGGCTATTTGAGGC[-/GT]GTGTGTGTGTGTGTG | 93664 |
rs143342224 | in-del | -/TCA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122761399 | GATGCTCACAAAGTA[-/TCA]ATGCCAGATCACAAA | 93664 |
rs143348471 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122409752 | TCTTGCCATCCCACC[C/G]TGGGTTGGTAGGAAG | 93664 |
rs143357953 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122448385 | CCCACCCTTGACAAA[C/T]GGGGATTATTACAAT | 93664 |
rs143358625 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122545615 | AAATGGGAACATCGT[A/G]GAAAAGTCCTTGAAC | 93664 |
rs143362101 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122546162 | TAAAATTGTGGTGAT[A/G]TTTCTTTTTATAATC | 93664 |
rs143363782 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122630877 | AAAAACAGGCAAGAT[G/T]TTCTTAAAGTAAATC | 93664 |
rs143367575 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | CADPS2 | GRCh38.p7 | 7:122710456 | AGTTTCTGCTACATG[C/G]TAGCCATTTAAGCTG | 93664 |
rs143377603 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122352304 | GTGTCAATTAGAAAA[C/T]ACTACATGAGGACTT | 93664 |
rs143391455 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122445742 | ATCGCTTGAGCCTGG[C/G]AAGTTGAGGCTGCAG | 93664 |
rs143392624 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122863691 | AGTTGATCTTGATCA[C/T]GTAAACACCATTAGG | 93664 |
rs143396896 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122777013 | AAAATTAGCCAAGCA[C/T]GGCAGTGTGTGCCTG | 93664 |
rs143399185 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122744063 | ACTTGATAGGTATAG[A/C]CATGGTCAAATGACC | 93664 |
rs143404177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122668232 | ATAAGAGAGGGAAAA[C/T]TGGAAAATTCCATTT | 93664 |
rs143411687 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122794281 | TAATCCCATATTTCT[C/T]GGAGGTTTTGTTCAT | 93664 |
rs143411779 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122742463 | AACACTTTGAAAACT[A/G]TAAGATTAAGCAAAT | 93664 |
rs143418147 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122665166 | TGATCATACTACTTG[C/T]ACCACACTTCCACGC | 93664 |
rs143422443 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122419884 | AACTCTGCATGTTTG[C/T]ACATTTTACAATGCA | 93664 |
rs143425601 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122873879 | TGGCATGAGATGATA[A/T]CTCGTTGTGGTTTTG | 93664 |
rs143425734 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | CADPS2 | GRCh38.p7 | 7:122520613 | TAATATTCTCTATGC[C/T]AGATTTTATATAGAA | 93664 |
rs143429900 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122555763 | TCAAGTTGTTAGGGA[C/T]AGTCTTTACCAATTT | 93664 |
rs143433925 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122638963 | CCTCTAGTCTGCCAC[C/T]TTGAACCCTAAGTCC | 93664 |
rs143436439 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122546524 | TTCCATAAACACTCA[C/T]TTTCTCCTCTTTAGA | 93664 |
rs143437775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122677436 | ACAGTGGAATGGGAG[A/G]TGCCTGAGGAGGACG | 93664 |
rs143441880 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122648803 | ATGCAAAAACAGTCT[C/T]GTAGATGAAGTCCAG | 93664 |
rs143444496 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122631525 | CTCAAGTGATCTTCC[C/T]GCCTCTGCCTTCCTA | 93664 |
rs143444984 | in-del | -/AGAA | 0.0295035 | 0.117819 | intron-variant | CADPS2 | GRCh38.p7 | 7:122398410 | CTTTAGTGGATTACT[-/AGAA]AGAATGATTTTTCTC | 93664 |
rs143455305 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122371796 | CTTGAGCAGATTCTA[C/T]AAAGACAGGGACACT | 93664 |
rs143466544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122808673 | AGAGGTATAGTACCC[C/T]TATGGCTTTTTCTGA | 93664 |
rs143470916 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | CADPS2 | GRCh38.p7 | 7:122874108 | CTCCCATTCTGTAGG[C/T]TGCCTGTTCACTCTG | 93664 |
rs143472172 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122494221 | GTTCCAGCCTGCTGG[A/C/G]CTTTCTGGAGAACTC | 93664 |
rs143482029 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122636784 | CCTTTTTAAGATTTT[G/T]TTGTTGTTGTTGAAC | 93664 |
rs143482658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122325032 | AAAGGATTTGGGCAA[C/T]GACAATGTATTACTT | 93664 |
rs143489100 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122421016 | TATCTCCTGGCACAC[C/T]GGACTGGGCTGCCTC | 93664 |
rs143496641 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | CADPS2 | GRCh38.p7 | 7:122572202 | ATATGCTGCAAGATG[A/G]AATGGAAATTCTTTT | 93664 |
rs143497708 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122828761 | ATCTGAGACTGTTTT[C/T]TCCCCTTTTACTTTC | 93664 |
rs143500261 | in-del | -/T | 0.079617 | 0.182947 | intron-variant | CADPS2 | GRCh38.p7 | 7:122360734 | CATGATGAACTGCAA[-/T]TTTTTTTTTAAAGAA | 93664 |
rs143525347 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122425959 | TTTTTTCCATACTCA[A/T]GGAGAATGTTTGCCT | 93664 |
rs143541997 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | CADPS2 | GRCh38.p7 | 7:122682318 | GAAAAGCTTCTACAC[A/G]TAGCCACAAAGTCAA | 93664 |
rs143555920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122745060 | GTTTTGATATGTTAC[A/G]CTGTTAAATAATTAA | 93664 |
rs143561063 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122784940 | TTTCACCTTGTTGAA[C/T]ATCAATTATTTTCAT | 93664 |
rs143564214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122668845 | GCCCTGTCTTCCCCA[C/T]CACCACTTTATTCAT | 93664 |
rs143569966 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122815444 | CTCAGAAAAGTTCAT[C/T]CACAATTTGTAACAA | 93664 |
rs143572788 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122706974 | TCTTAGGTTAATCAT[A/G]ATTTATCCTGTTGTA | 93664 |
rs143575096 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122726078 | ACTCTAAATAAAACT[C/T]CCATTCACCCATCTG | 93664 |
rs143576684 | in-del | -/AAC | 0.0681886 | 0.171594 | intron-variant | CADPS2 | GRCh38.p7 | 7:122664431 | ATAAAATAAAATAAA[-/AAC]AACAATAGAGACAAC | 93664 |
rs143592565 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122353594 | ATGTTAATAAGACCA[C/T]TTTAAATAGGGATTT | 93664 |
rs143599076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122485527 | TGACAGCTGAGAGAG[A/G]TGAAGAAGCCTCTGC | 93664 |
rs143603388 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122577013 | TGATCCCCCTGCCTC[A/G]GCCTCCCATAATGCT | 93664 |
rs143608339 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CADPS2 | GRCh38.p7 | 7:122613766 | ACTAATATATTACCC[C/T]CAAATATATACTGTG | 93664 |
rs143616363 | snp | A/C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CADPS2 | GRCh38.p7 | 7:122319624 | GACCAATTCAAAGTA[A/C/T]TAAGAACCAAGATTA | 93664 |
rs143621312 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122590489 | GACATTCCCCTTGTA[C/T]GGCTGCGCTATAATT | 93664 |
rs143635520 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122835513 | GAAGTTCGAACCCAA[A/C/T]GCAAAGAAGCTAAAA | 93664 |
rs143647344 | in-del | -/AGA | 0.0178098 | 0.0926698 | intron-variant | CADPS2 | GRCh38.p7 | 7:122678872 | AGCTGAAACCATGGC[-/AGA]AGAACATAAATTGTG | 93664 |
rs143669355 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122380584 | TCCCCAAGGGTTCTG[A/G]CAGTTACAAGTGGTT | 93664 |
rs143673060 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122473456 | AAAGCTCAAAGGAAA[C/T]TGATTTTGGATTTTT | 93664 |
rs143675207 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122770746 | GCATTATAGATGGCG[G/T]CACCCACAGGGCAGA | 93664 |
rs143675458 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | CADPS2 | GRCh38.p7 | 7:122583263 | TAAGTGTCCATAAAA[C/T]GAGATTCAGTTAAAG | 93664 |
rs143686109 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122787036 | CCTTGTAACAGTATG[A/C]AGGACTGTTTGGAAA | 93664 |
rs143686809 | snp | C/T | 0.161924 | 0.233971 | intron-variant | CADPS2 | GRCh38.p7 | 7:122658591 | TCCTTTGTAGGGACA[C/T]GGATGAAGCTGGAAA | 93664 |
rs143703316 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122442479 | GAAATCTGCAAACTA[A/G]TAACTTGGAAAGAAG | 93664 |
rs143710594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122788823 | CACTTTGTTCCTTGC[A/G]TTCATTTGGGCCTAA | 93664 |
rs143717789 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122617719 | TCATGGGATCTGCTA[G/T]CCTAATATCAATGAA | 93664 |
rs143720485 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122700573 | TCAATACAACAATAC[C/T]TAAATCTTTCTGTCT | 93664 |
rs143727865 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122859328 | TCCTTCTAATTTTTT[-/T]ATTCCTGTCTTAATG | 93664 |
rs143734551 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122321433 | TCAGCCTCCCAAAGT[A/G]CCGGGACTACAGGCC | 93664 |
rs143740538 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122512233 | GATGGATGGCTGTAC[A/G]TACTCACTGGAAGAC | 93664 |
rs143741750 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122869839 | GTGAATGGGAAAAGA[G/T]TAAAAGTATAGAGTT | 93664 |
rs143749435 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | CADPS2 | GRCh38.p7 | 7:122835868 | CTGAAGGATATTATC[C/T]GGGAGAACTTCCCCA | 93664 |
rs143750446 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122635018 | CGTCCAAAAGGATGC[C/T]TGGTAGTATTTCAAT | 93664 |
rs143753569 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122749443 | ACCTGAACTAGCAAA[C/G]TGTACATAAAAGACT | 93664 |
rs143754257 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122524666 | AATATTTTCCATAGA[A/C/G]TATCTGTAACAGTCA | 93664 |
rs143768208 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122367288 | CTAAGTTATGAGAGA[C/G]AGAAAGCGAGAGAGA | 93664 |
rs143770923 | snp | C/T | 0.000127815 | 0.00799321 | intron-variant | CADPS2 | GRCh38.p7 | 7:122471359 | CATTTCACTTTGTAT[C/T]TGCAAGTAAAAATAC | 93664 |
rs143774689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122456935 | GCATTCTAAAACAAA[C/T]GCAAAAACTCTTTTA | 93664 |
rs143780711 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | CADPS2 | GRCh38.p7 | 7:122495697 | CTAGGTTGTTGGGTG[A/C]ACAGATCTTCATCTT | 93664 |
rs143782551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122566561 | GTGGATATTCTAAAG[C/T]GACTTTGAATAGCTC | 93664 |
rs143797238 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122651817 | CTTAATCATTTTAAG[A/C]GACAAATATAGAAGT | 93664 |
rs143810731 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122375253 | TAACCAAAACAATTC[C/T]GAGCAAAAGAATAAA | 93664 |
rs143816627 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122822995 | TTCACATGGACACGC[A/G]TGAAAATTTTCACTA | 93664 |
rs143822294 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122761299 | CTCCACTCATTCCTG[C/G]AACATGGGCAGCCAG | 93664 |
rs143824083 | in-del | -/CT | 0.0325976 | 0.123435 | intron-variant | CADPS2 | GRCh38.p7 | 7:122865156 | ATCTCCTCTCTCACA[-/CT]CTCTCGTTTCTTCTC | 93664 |
rs143827611 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122707327 | CTATAACTTCCAGGC[A/G]CCAATTAAATTTTTT | 93664 |
rs143832456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122683542 | GGGTACAACGTGATG[C/T]TTTGATATGTGCTTA | 93664 |
rs143852130 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122568633 | CAGACTGTGCTAGAA[A/C]AACATGTTCAAATAA | 93664 |
rs143886158 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122453372 | TCAATTCCCATTGAG[C/T]GAATGTTAATACAAA | 93664 |
rs143891926 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122575033 | CAAAACATTATGTAG[G/T]TGGATGCTTGGCAAA | 93664 |
rs143893591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122354941 | TCTAGATCAGAAAGA[C/T]ATCAAGGAGAATCCT | 93664 |
rs143893969 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122519790 | ATATGATGTAGATGT[A/G]TAGAATATATTTTAT | 93664 |
rs143899651 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122646527 | GGAGAAGTAGGAATT[C/T]CAAATGAAGAGAATA | 93664 |
rs143905258 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122665180 | GCACCACACTTCCAC[A/G]CCTGTCTGCATGTGG | 93664 |
rs143927524 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122765102 | TCTGACACTTCCATG[G/T]ATTATACCAATTGGG | 93664 |
rs143931943 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122686845 | ATGTGTCACTACGCC[C/T]GGCTAACTTTTGTAT | 93664 |
rs143932775 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122644958 | TCTTGTAGAACAGTT[A/G]TAAGGGTCTTAAAAA | 93664 |
rs143951812 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | CADPS2 | GRCh38.p7 | 7:122423712 | TCTCCATTTCTTGGC[G/T]TAAGCATGCATCAGA | 93664 |
rs143952546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122782468 | CAACAAAAATTAGCA[C/T]GGTGTAGTGATGCAT | 93664 |
rs143958199 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122542325 | TATGTATTAACATTT[A/C/T]ATTATTCATATATAT | 93664 |
rs143962367 | in-del | -/TG | 0.134119 | 0.221521 | intron-variant | CADPS2 | GRCh38.p7 | 7:122449868 | CCAGCACTAAATGAC[-/TG]TCCCTACCCCTGGTT | 93664 |
rs143977417 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122813701 | ATTCTAAGGAAAAGC[C/G]TTATCCCAATTATTT | 93664 |
rs143979714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122724677 | GGTTACATAAACTCC[A/G]TCAGTCACACAGATC | 93664 |
rs143985667 | in-del | -/CT | 0.0715223 | 0.175059 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122558833 | ACATTTGTGCATAAA[-/CT]CTGTGATCTGTGAAA | 93664 |
rs143992141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122347566 | TAACTATATAAATGT[C/T]TTTACTGGTCTCTCC | 93664 |
rs143993545 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | CADPS2 | GRCh38.p7 | 7:122838109 | CTTCATCCCTGGGAT[A/G]CAAGGCTGGTTCAAC | 93664 |
rs144006123 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | CADPS2 | GRCh38.p7 | 7:122615667 | CAGTGCAGATGATAA[C/T]AGCAGTACATGATAA | 93664 |
rs144006271 | in-del | -/TG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122745124 | GTTACCTTTTGTGTC[-/TG]TGTGTGTGTGTGCAT | 93664 |
rs144010977 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122855979 | AAAAAGAAGTTGAGG[A/T]GGGGAGGGGTGCTCC | 93664 |
rs144020432 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122685073 | TTTAACAGATGGCAA[C/G]TACATGTGGAATAGC | 93664 |
rs144026326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122403451 | AAAACTGAGTGCTCA[A/G]AAGAGATTAGTACTA | 93664 |
rs144047089 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817390 | TCAACCACTTTCTCC[C/T]TTCCACTCTTCAATC | 93664 |
rs144052838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122727932 | TGCAAATTTAGAATA[C/T]CACTTCTCATTACTG | 93664 |
rs144072026 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122552242 | CTATCTTAGCATAAC[A/G]TCATCACAGATAATT | 93664 |
rs144073385 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122548577 | ATATGGATCAAATCA[C/T]ACTTATTTAATGATT | 93664 |
rs144074284 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122492259 | GTTGAGAATTTAGTG[G/T]CCACATAATGAAAAC | 93664 |
rs144091241 | in-del | -/GAA | 0.00636936 | 0.0560724 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122537395 | GTGTAATGCTATGAT[-/GAA]GAAGATTCTTTCTTA | 93664 |
rs144100345 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CADPS2 | GRCh38.p7 | 7:122397928 | GGGGAAAGCCAGCAC[C/T]TATTTTTCAGATAAA | 93664 |
rs144103139 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122454635 | CAGTTAAAGAAGACC[A/G]TAAGAAAGGAAGTCC | 93664 |
rs144135171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122401597 | CTCAGTATCATTGAA[C/T]CATCGTGCCAATTAC | 93664 |
rs144136213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122824181 | TGTTTGCTTATATCA[C/T]TTGATTCTCACAGCA | 93664 |
rs144142404 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | CADPS2 | GRCh38.p7 | 7:122787162 | TCAGCTGAATGATTT[C/G]AGCGTAGATATCTAA | 93664 |
rs144145115 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122543996 | TACTGGTAGAACTAT[C/G]TAGTAAAACTTGAAA | 93664 |
rs144150414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122710325 | AATCCCTCCCGTGAA[A/G]GAGCAGAGAAAAACG | 93664 |
rs144153623 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | CADPS2 | GRCh38.p7 | 7:122646677 | GCAGATGGGGCCACA[C/T]TGAACACCACAACTG | 93664 |
rs144175639 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122449720 | ATCATTTCAGGCAGA[C/G]AATTCAATCTTAACT | 93664 |
rs144186051 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122881857 | ACATGTTTAGGAACA[C/T]TAGTTCCCACTTTCC | 93664 |
rs144193356 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122743846 | CATCAGTGTCTTCCA[A/T]GTTTTTGAAATAACA | 93664 |
rs144198049 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | CADPS2 | GRCh38.p7 | 7:122667404 | AATCACATTTTTGAA[A/G]CAAGGACACCAAGAA | 93664 |
rs144202363 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122784716 | AAGGTAACTTTAGTA[-/T]TTTTTTTTTTCTGGA | 93664 |
rs144208697 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122804927 | CAATGAATAAGCTCT[C/G]GGGATTGGTAAATAG | 93664 |
rs144217098 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122472612 | CCATATTACACTGGC[G/T]GTCAACAACAAAATC | 93664 |
rs144218979 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122719711 | TAAATTCTATGTGAT[A/G]TAATAATTTTTAGAA | 93664 |
rs144219835 | in-del | -/A | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122351060 | TAAAAACCATGAATG[-/A]AAAAAAATCTCATTG | 93664 |
rs144224450 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122603647 | TCAAACAGATATAAA[C/T]AGCCATAGTAACACA | 93664 |
rs144235570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122791132 | GATTGTATCAACGGC[A/G]CGAGGAAAAGTACAA | 93664 |
rs144247154 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122321153 | CCCTTATGTTTACAT[C/T]GATTGATTGATTGAC | 93664 |
rs144247509 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122417574 | TTTCATCTGTTTCAT[C/G]AACATTTCAACATCC | 93664 |
rs144255966 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122327457 | TTTCTTGTTGAAGGA[C/G]AGAAACTATATATAT | 93664 |
rs144270263 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122422954 | ACAGAGTGAGACTCC[A/G]TCTCAAAATAAATAA | 93664 |
rs144290999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122674654 | AGCCCTTATTGTTCA[C/T]ACATTGCTGTTGATT | 93664 |
rs144301359 | snp | C/T | 0.000101411 | 0.00712007 | intron-variant | CADPS2 | GRCh38.p7 | 7:122581325 | ATGTTTCTTAAAATG[C/T]AGCATTATTTTTTTC | 93664 |
rs144309961 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | CADPS2 | GRCh38.p7 | 7:122341372 | GTCATCATTGCTAAC[A/G]TTAAAACTAAAAAAA | 93664 |
rs144316782 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122747947 | GTCATCTTATCCTCT[C/T]TGTGCCACTTCTGTA | 93664 |
rs144320269 | snp | A/G | 0.185788 | 0.241613 | intron-variant | CADPS2 | GRCh38.p7 | 7:122723915 | CCATCATTCTCAGCA[A/G]ACTGTCACAAGGACA | 93664 |
rs144323272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122483042 | AGTATTAAGAAAGAT[A/G]TTGGTCCAGAAATGG | 93664 |
rs144338281 | in-del | -/AAATAAAATA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122374409 | CCAAAGTAAGTAGAC[-/AAATAAAATA]AAATAAAATAAAATA | 93664 |
rs144344682 | in-del | -/A | 0.0368353 | 0.130617 | intron-variant | CADPS2 | GRCh38.p7 | 7:122344538 | GACCTTAGTGCTGAT[-/A]AAAACTGTAATACTG | 93664 |
rs144350881 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122853805 | AAGAGAGGGGAAGCA[A/G]GAGCGAAAAGCGGAT | 93664 |
rs144353079 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122767289 | TTACAACTGTGAGGT[C/T]GATGTTATTATTCCT | 93664 |
rs144354382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122431289 | TCTTGGCACTGTGGA[C/T]AAGAAGTTGTTAAAA | 93664 |
rs144357660 | snp | A/C/T | 0.0236965 | 0.106392 | intron-variant | CADPS2 | GRCh38.p7 | 7:122570863 | ACAGGAAGGGGAACA[A/C/T]CACACTCTGGAGACT | 93664 |
rs144362482 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122659887 | AAAAAAAAATCTAAC[A/C]GATAATTCTATATCC | 93664 |
rs144386637 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122401693 | GATACCATTTAAACT[G/T]ATTGCCCATTAAATT | 93664 |
rs144387811 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122825659 | AACATTTTTCCTTAA[A/T]TTTTATCTTTACATT | 93664 |
rs144395659 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122537880 | AATAATTTTAAAAAA[G/T]GATAAAAACGCAAGA | 93664 |
rs144401316 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122322309 | CAGAGCAGATTTGAA[C/T]TGTGGATCTGCAGTC | 93664 |
rs144409437 | snp | A/G/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122418838 | AGCACTAACTACATT[A/G/T]CCACATAAGTGTGAT | 93664 |
rs144415599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122482620 | CTGCACGTTGGGCAA[C/T]GTGATTCCTGAGGGA | 93664 |
rs144445560 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122628280 | ATTTTCTTTGCAGAA[G/T]TAAAAAAATAATTGT | 93664 |
rs144452351 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122820298 | CACAAAGCTTCACAG[A/T]TAGCCCCCATTACTT | 93664 |
rs144453030 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122405838 | ATTGGATAGGAGAAT[C/G]AATAAGACTAACAAA | 93664 |
rs144457621 | snp | C/T | 0.030278 | 0.119257 | intron-variant | CADPS2 | GRCh38.p7 | 7:122821666 | GATAACAGGTGAGCC[C/T]TTATTAGTCAAATCA | 93664 |
rs144468325 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122627286 | AAATAATTCAGCAAG[G/T]TCAGTCAATTGTTAT | 93664 |
rs144469640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122634040 | AGGAATACTGCTTGA[C/T]TGCTGTGAATTAACT | 93664 |
rs144489815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122364872 | ACATGAACATAACTG[C/T]ACATGACACAAGGCA | 93664 |
rs144491195 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122468446 | AAATTAGGAATATAA[G/T]TACATACACATTGAA | 93664 |
rs144497571 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CADPS2 | GRCh38.p7 | 7:122492500 | GAATGTTTCATTAGC[C/T]CAGTTTGGGTCAAGA | 93664 |
rs144501076 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122564636 | GAACTAAAAATAGAA[A/G]TATCATTAGATCCAG | 93664 |
rs144501444 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122618795 | CCTGTGACTAGAGGC[A/G]TATCTATTCTCTCTG | 93664 |
rs144522583 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122879946 | CATAGCAGAACTTAA[A/C]CAAGTCATTTTAATT | 93664 |
rs144528590 | snp | C/T | 0.030665 | 0.119967 | intron-variant | CADPS2 | GRCh38.p7 | 7:122795390 | CTGGACACATACACC[C/T]TCCCAAGACTCAACC | 93664 |
rs144534219 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122561415 | TATCCTAAGTGGATA[C/T]ATTTTCCTTGACATT | 93664 |
rs144540189 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122694423 | TGGACATGTGTAGAA[A/G]AGTTTTGAAATCAGA | 93664 |
rs144541897 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122742673 | CTGACTTACATTGTG[C/T]TTATAATCAACAAAA | 93664 |
rs144559314 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122474038 | CTTAAAATGTCTGTA[A/C]GTCCTATAACAGAGG | 93664 |
rs144563955 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122412282 | TGTAATCTAGTTGGT[C/T]GACAGGAAATCGATT | 93664 |
rs144570247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122548037 | TGTAGACAGTAAGTA[C/T]TGAGTCAGCTGTTTA | 93664 |
rs144572603 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122517036 | AAAAGTTCCCTTATG[C/T]CCTTTATGATCAATC | 93664 |
rs144575997 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122565198 | TATAACCATGTAACA[C/T]GACTGCACTTATACC | 93664 |
rs144579074 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122608993 | AGGAATTTGAGACAA[A/G]CCTGGGTAACATAGT | 93664 |
rs144595413 | in-del | -/TTAT | 0.492877 | 0.0592508 | intron-variant | CADPS2 | GRCh38.p7 | 7:122526180 | TATCCTTTGATACAC[-/TTAT]TTATTTATTTATTTA | 93664 |
rs144598894 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122643927 | AAAACCCCTCTCTAC[C/T]AAAAATGAAAAATTA | 93664 |
rs144616316 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122415318 | TCTAAACCAAAGCAA[G/T]CATGGCATAGGGGGA | 93664 |
rs144618340 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122514177 | ACACTCCCTACAAAA[C/G]TGGAAAATATTGCTA | 93664 |
rs144620834 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122369284 | TACATGTGCCCGCCA[A/C]CATGCCCGGCTAATT | 93664 |
rs144626840 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122759870 | AAGAAGCAAAATCTA[A/C]ATAGGATTATTCCTA | 93664 |
rs144630018 | in-del | -/GGGGGGGG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122777345 | AGATCCAGTATGGCT[-/GGGGGGGG]GTTGGAGCTCCAGCT | 93664 |
rs144632664 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122460806 | AATCAAACAGAATAA[C/T]AGAATTTCCAGGACT | 93664 |
rs144641181 | in-del | -/GTGGTGGTGGTGGTGGTGGTG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122528111 | TAGATGAAGGCATTA[-/GTGGTGGTGGTGGTGGTGGTG]GTGGTGGTGGTGGTG | 93664 |
rs144656220 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122422578 | CTTTGGGCACATAAA[C/T]AAATTGTTCTAATTA | 93664 |
rs144657282 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122843229 | AATCACACATCATAA[A/G]AGTTGCTTTTTTTTT | 93664 |
rs144661109 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122757333 | TTTGTATTTTTTGTA[A/G]AGACGGGGTTTCGCC | 93664 |
rs144661828 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122868934 | AACAGACAGGTTGAA[C/T]AGCAGCCTAAGTCAA | 93664 |
rs144661968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122523158 | TCCAAGCTGTTTTCC[A/G]TAATGGCTGTACTAG | 93664 |
rs144677363 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122560695 | AAGTAGAGCCTATCT[C/G]TACAAGAAACCTTGA | 93664 |
rs144689450 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | CADPS2 | GRCh38.p7 | 7:122373866 | ACACTACCAAAAAAA[A/C]CCCCAAAAAACAGAA | 93664 |
rs144704009 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122690996 | TGTACCTCCGGCCCC[A/G]TGGCCTTATCTTGCA | 93664 |
rs144709799 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122510680 | AGGGGTATACTGTCC[C/T]CCCTGTGAAAACGAT | 93664 |
rs144717804 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122604330 | TCCATTTGCTCTCTA[C/T]AGCAACACTCTCAAG | 93664 |
rs144724878 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122346265 | CCCAGCTAGCCAGGA[C/G]GGTGAGGCAGGAGAA | 93664 |
rs144735234 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122716571 | CATTAGGAGATATAC[C/G]TAAGGTAAATGATGA | 93664 |
rs144738126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122574204 | GAATCCAAGCAATCT[A/G]GGGGGCTGAGGTGGG | 93664 |
rs144740955 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122809677 | TTTATAATGGTCCAA[C/G]GAAAGACTAATTATA | 93664 |
rs144757791 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122875482 | CAAAAATAAGATAGG[A/G]ATGATTACTATAATA | 93664 |
rs144760388 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122365231 | ATTTCAAAAGTAGTG[C/G]AGAGTCTTTCCTCAG | 93664 |
rs144765712 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122335764 | ATTAAAGGGCTAGAA[A/T]AAAAGGCCTACAAAG | 93664 |
rs144767113 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | CADPS2 | GRCh38.p7 | 7:122761425 | ACAAATTAATAAGCC[C/T]CACCTATATCCTGAG | 93664 |
rs144769152 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122429286 | GCTTTTTTTTAAAAT[A/C]TATATCACAAAACTA | 93664 |
rs144769224 | snp | A/G | 1.64879e-05 | 0.00287118 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698392 | CTCCCCACCTCAACC[A/G]CGGCTGTAATGAGAA | 93664 |
rs144770992 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122684837 | TAAGGATAGCACGTT[A/G]TTTACTCTTGATAAT | 93664 |
rs144781646 | in-del | -/A | 0.220037 | 0.254694 | intron-variant | CADPS2 | GRCh38.p7 | 7:122610323 | ACTTTTACTATTTGT[-/A]AAAAAAAAAGTGTTA | 93664 |
rs144786700 | in-del | -/TATA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122708473 | GTGGATATATATATA[-/TATA]TATATATATATTGGA | 93664 |
rs144794886 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122843856 | AACAGGAGGCAAAAG[C/T]GTAAAGTGAAGAAAG | 93664 |
rs144804429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122758418 | GCGTATGTATTATAA[C/T]GACCACAGGGGTAAA | 93664 |
rs144815638 | in-del | -/AATTT | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122479783 | CCCTATGAAGTGTGA[-/AATTT]AATATATTAGATCAA | 93664 |
rs144824684 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122591138 | GCAACTTCAGCAAAC[A/T]CTCAGGATACAAAAT | 93664 |
rs144830260 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122355758 | GACAGAACATTACAG[C/T]TAAAAGAACTAATGC | 93664 |
rs144834693 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | CADPS2 | GRCh38.p7 | 7:122681432 | GCCATTAAGAAATTC[A/G]TCATTCGAAACATAG | 93664 |
rs144846425 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122580374 | GCACAAGAATCGCTC[A/G]AATCTAGGAGGTGGG | 93664 |
rs144854391 | in-del | -/TGTTAG | 0.0626037 | 0.165477 | intron-variant | CADPS2 | GRCh38.p7 | 7:122486923 | GAAGTCTCAGGTGAT[-/TGTTAG]TATTTTTAGCAATAA | 93664 |
rs144857492 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122339951 | AGAGGCAAACAAGAG[C/G]ATGTAAGTGCAAAAT | 93664 |
rs144858210 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | CADPS2 | GRCh38.p7 | 7:122840196 | AGAAAACCAAATACC[A/G]CATGTTCTCACTCAT | 93664 |
rs144865971 | in-del | -/GAGGTTGAGGTGGGCGGATCAACT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122827417 | TCCCAGCACTTTGGG[-/GAGGTTGAGGTGGGCGGATCAACT]AGGTTGGGAGTTTGC | 93664 |
rs144869009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122759420 | ACTGTTTGAATAAAG[C/T]TATGTTTCTTTTCTA | 93664 |
rs144875445 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122394061 | TTCACTAGGAGGGTG[C/T]CTGTGGGTTTGGGAA | 93664 |
rs144876518 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122424620 | ACAGAGAATAGATTA[C/T]TAGAACCCACAAGCA | 93664 |
rs144879203 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122652251 | TCTCTCTCTCTCTCT[A/G]CATATATATATATGC | 93664 |
rs144882104 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122720503 | ATGTATATGTATATA[C/T]GTATAAGTATATATA | 93664 |
rs144882262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122526485 | GGCATGAGCCATCCC[A/G]CCTGGTCTTCTTTGA | 93664 |
rs144887119 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122755900 | CGATGTAGACGTTTT[C/G]CTGGATTCCACATTA | 93664 |
rs144892177 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122645276 | ATACATGTACATATA[C/T]ACACACATATGTACA | 93664 |
rs144897395 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122677912 | AGCATTCCGCAGCTT[C/G]ATGGTATTTCTCTAT | 93664 |
rs144898246 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | CADPS2 | GRCh38.p7 | 7:122387332 | GGGTGGGATGCTTTT[C/G]TTTTCAAGTGTCTCA | 93664 |
rs144906894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122772929 | GTCAACAATTTTAAA[C/T]AGACAAAATTTCTGT | 93664 |
rs144909991 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122375685 | ACATAGGGAAAAAGT[G/T]TCTTGACATTGGCCG | 93664 |
rs144911166 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122694196 | TTACAATTGCTTCTA[G/T]GCTGAAGCTGGAAAA | 93664 |
rs144923746 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122345335 | TAGAGACGGGGTTTC[A/G]CCATGTTGGCCAGGC | 93664 |
rs144929090 | in-del | -/T | 0.0433465 | 0.140692 | intron-variant | CADPS2 | GRCh38.p7 | 7:122326201 | TCTTAGGAAGAAACA[-/T]TATCAAGATTGAATT | 93664 |
rs144943212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122718695 | TATAATCCAAGCATT[A/G]CAACACAACACTTAA | 93664 |
rs144944693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122718302 | ATATCTGGAAATTTC[C/T]TGACATGGAAAAATG | 93664 |
rs144946971 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | CADPS2 | GRCh38.p7 | 7:122761417 | GCCAGATCACAAATT[A/G]ATAAGCCTCACCTAT | 93664 |
rs144948341 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122445526 | ATATATTAATATTTA[C/T]ATATTTATCACAGGG | 93664 |
rs144954222 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122587827 | TAATTTACATTCCCA[C/T]CAACAGTGTAAAAGT | 93664 |
rs144955861 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122536933 | GCTGATATCTGAAAA[C/T]ACCACATGTTTTCAC | 93664 |
rs144956520 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122576099 | TCATGTCTCCTTAGT[C/T]TCCTCTGATTTGTGA | 93664 |
rs144959141 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122392863 | AGAATCCTCAAAATG[C/T]TTTGTATACATAAGG | 93664 |
rs144971633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122844266 | TGGATTTCACATTTG[C/T]ATGAAACTTTATCCT | 93664 |
rs144976340 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122484580 | ATGTTTGCAATTTGG[A/G]TTAGGCAAAGATCCT | 93664 |
rs144980667 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122542114 | CTAGTTCATTTAATC[A/C]TTACAGCATCATTTT | 93664 |
rs144988581 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122627493 | TCAACATCTCTGATG[A/G]AACCATTAGGGTTCT | 93664 |
rs145007541 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817867 | CTTATTTCCATGCCC[C/T]GACCTCTTATCTCTG | 93664 |
rs145013533 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122440822 | AATGGGAGTTGGCCA[C/T]ATTATTTAACTGTTA | 93664 |
rs145024199 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122780785 | AGTGTTAGCCGTTCT[C/T]TTAAGGGCTGTATAA | 93664 |
rs145027837 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | CADPS2, RNF148 | GRCh38.p7 | 7:122701477 | GATAGCATTTGGAGA[C/T]ATACCTAATGTTAAA | 93664 |
rs145037903 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | CADPS2 | GRCh38.p7 | 7:122393996 | CACAGAGGAGCTAAA[C/T]CTTCTCAATTCTAAG | 93664 |
rs145040739 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122597958 | AACATGGGACATTAT[C/T]CTAATAAAATATTAT | 93664 |
rs145047241 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122629077 | AATAATATGCTTCAT[G/T]TAGATAACATGCTTT | 93664 |
rs145047838 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122489046 | GCTACTAATTTTAAA[A/G]AAGAAATTTTAAATC | 93664 |
rs145056672 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122583684 | GTACGTGTGTATATA[C/T]GTATATACATATGTC | 93664 |
rs145084591 | in-del | -/TG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122384825 | ACAATGTTCATCATT[-/TG]TGTGTGTGTGTGCCT | 93664 |
rs145089442 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122827735 | TAACTCATTTTATGA[A/C]GGTGGCATTATCCTG | 93664 |
rs145091854 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122358542 | AAATCCAAGGCCATA[A/T]ATATTTTATCTTATA | 93664 |
rs145097840 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122450039 | CACAGAGTCTAAGAC[A/C]TTTATATTATCAGGA | 93664 |
rs145101205 | in-del | -/TG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122645386 | ACACACATATGTACA[-/TG]TGTGTGTATATATGT | 93664 |
rs145102172 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | CADPS2 | GRCh38.p7 | 7:122490464 | AACAATAACAAAAAG[C/G]GTTAAGCTCCCATAT | 93664 |
rs145114480 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122582808 | AAATAAAAGATTTTT[G/T]ATAGTCATATAGAAA | 93664 |
rs145119465 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539256 | GCAGTGAGATCCTGA[C/T]GAAATGATGAATTCA | 93664 |
rs145129994 | snp | A/T | 0.0248432 | 0.108648 | intron-variant | CADPS2 | GRCh38.p7 | 7:122624413 | AGTCACTTTTTCTTA[A/T]GCGCTCTTAACCTTC | 93664 |
rs145154794 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122419616 | ATTCTCAAAGTTGTC[C/T]ATAAACCAAACAGAT | 93664 |
rs145162767 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122832365 | TAAAACTTTTAAAAA[C/G/T]TGTGAGCTTAGAGAC | 93664 |
rs145169985 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CADPS2 | GRCh38.p7 | 7:122696809 | AAACAGTCAAGTTTT[C/T]CAAATTAACACATAA | 93664 |
rs145181115 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122389338 | AACTTAGTGCAAGGT[A/G]TTGTCTGACAGAGAA | 93664 |
rs145188162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122371592 | AAGATGAGATTTTGG[A/G]TGGGAACACAGCCAA | 93664 |
rs145201332 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122459018 | TATGAGAAGAGAAAT[C/T]TGAAAAATAAAGACC | 93664 |
rs145209126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122610863 | ACTAGTGTTCTTCCA[A/G]TGGGTTTCAGAACTG | 93664 |
rs145212120 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122779179 | TTTTATAAATTATCC[A/C]GTCTTGGGTATTTCC | 93664 |
rs145212687 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122667650 | GCAGCAATGGAAACC[A/C]ACACAGAGGGAGAAA | 93664 |
rs145213427 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122455219 | AGTGCTGCTGCTTCT[A/G]CCTGAGAGTGCTTTC | 93664 |
rs145219655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122553878 | CATAGTAAGTCCAAA[A/G]TGTTATTCTGAGGAA | 93664 |
rs145239443 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122871240 | GACTTATGTATTCCA[G/T]CATTTTCACATGTTG | 93664 |
rs145243721 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122585409 | GAAAAATCATAAATT[C/T]TAGAATGAATAAATT | 93664 |
rs145243846 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122784840 | AGCCTTTTTACTTTG[C/T]GGGCCAAAATCTTTC | 93664 |
rs145262890 | snp | A/C/T | 0.00199529 | 0.0315338 | intron-variant | CADPS2 | GRCh38.p7 | 7:122862203 | ATTACTGCTGTACTT[A/C/T]GGAATAGTGATTCTC | 93664 |
rs145264090 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122619589 | CAGAGATAGTGCCAC[G/T]GTACTCCAGTTTGGG | 93664 |
rs145270089 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | CADPS2 | GRCh38.p7 | 7:122463907 | ATGCTGAAATGAATG[C/T]TGATGTCCTAGATTC | 93664 |
rs145271836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122737854 | TTAATAGGAAGAAAG[A/G]CTGAAAAGACAGAAC | 93664 |
rs145305888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122784394 | CTTTCTAAATACATA[C/T]GCACTCATGTGTTAA | 93664 |
rs145323831 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122518852 | TTTCTAATGAGTACT[A/G]TGAATTTTTTTCACG | 93664 |
rs145325486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122505803 | TCTGTTTCCATAAAA[C/T]GTTGCCATATTTCAT | 93664 |
rs145326495 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122563311 | TATTAGAGGATACTG[C/T]TTGAGTAGCTTTATC | 93664 |
rs145335148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122609770 | GTGTATTGGAAATAC[A/G]GACTAAATAAGGCAC | 93664 |
rs145349839 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122641330 | TTTAGTTCAGAAAAT[A/G]TGCTTTTATTTTCCT | 93664 |
rs145354418 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122606767 | AGAAGGTATAATACA[C/T]AGCCCTTGTCTTCAA | 93664 |
rs145357976 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122412938 | GTGATGCTGTGGTTC[A/G]AATCTGTCAGCAGAA | 93664 |
rs145362100 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122509815 | AATACCTACCTTCAC[A/G]GGCTTATTCTGATAA | 93664 |
rs145364052 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122327744 | TAATACAATGCCAAA[A/C]TAATAATTTTAGAGA | 93664 |
rs145371834 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122370561 | CAAGCAGTGTACAAA[C/G]AATAATAGATAAAGA | 93664 |
rs145373135 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122461576 | CTAGCATTTGTACTG[A/C]CAAGAGCCTTTTTTG | 93664 |
rs145401866 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122791133 | ATTGTATCAACGGCG[C/T]GAGGAAAAGTACAAT | 93664 |
rs145404912 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122712670 | CTGTTTGGGCTGTTA[C/T]AACAAATTACCATAA | 93664 |
rs145417558 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122845029 | GACTTAAAACTTCAA[A/C]TAAGGCTTCCTAGTC | 93664 |
rs145425542 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122760057 | TTATAGTACAATGAA[C/T]AATTTTACACACAGT | 93664 |
rs145435611 | in-del | -/A | 0.0379877 | 0.132479 | intron-variant | CADPS2 | GRCh38.p7 | 7:122801342 | GGTCCAATATGTATT[-/A]AAAAAAACTCCTAAA | 93664 |
rs145435640 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | CADPS2 | GRCh38.p7 | 7:122808314 | ATTTCTGCAGTTCGT[A/G]CCCTTGTGATTTAGA | 93664 |
rs145439395 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122721892 | CTGGTTCAATATACG[C/T]GAATCAATAAATGTA | 93664 |
rs145440246 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122344016 | AGGCAATACTTTTTA[A/T]TGTATGATAGCCTGA | 93664 |
rs145442061 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122558428 | ATTCGTTTCTCTTAA[A/C]CTTTCCGTATGCATT | 93664 |
rs145444617 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122689742 | GCCGCTTATTCCACA[A/G]CACCCTTGGTGTAGT | 93664 |
rs145452821 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122571857 | AAGTAGTTATCATGG[A/G]ACTTCTAAAAAACTT | 93664 |
rs145456138 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122867445 | CACTAACTCCACCCT[A/G]AGCACCCAAGAAGGA | 93664 |
rs145470498 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122850227 | GCCAAGTGACAGGGA[C/G]CCAGAGGCCCCCTGA | 93664 |
rs145474556 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122323344 | TATTTATTGGTCAAA[C/T]ATTGATCATTAGGAA | 93664 |
rs145481933 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122419644 | GATGCTAAGAAGCAC[C/T]GAACCAGATAATTTC | 93664 |
rs145490506 | snp | A/G | 0.00138484 | 0.0262774 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698716 | CCTGCCACTCTCTTC[A/G]AAGTGGAGCTTCTTC | 93664 |
rs145501567 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122408904 | CAGTAACTAAAAAGA[C/T]TGCCATGTAATTAAT | 93664 |
rs145505873 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122472316 | TGTAAGAGAAATAAA[A/G]AATAATGAGAAAAAG | 93664 |
rs145511563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122676889 | CAGTCAATGGATTCT[C/T]TGTTGGCACTGTTTT | 93664 |
rs145512411 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CADPS2 | GRCh38.p7 | 7:122397907 | CAAAAAGTGATTACC[A/G]CCTGAGGGGAAAGCC | 93664 |
rs145524562 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122619389 | CTAGCACTTTGGGTG[G/T]ATTGTCTGAGCTCAG | 93664 |
rs145534453 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122807074 | GGGCTTTCTTTCCTC[A/G]TTCCAGCACATTTGT | 93664 |
rs145539802 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122446184 | TGGTTTACTAATTCT[A/G]TATTTTGTGTCTTCT | 93664 |
rs145545751 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122391068 | TTATTTAATCAGCAG[C/T]TGTATTTTTAATTCT | 93664 |
rs145550177 | snp | A/G | 3.2969e-05 | 0.00405998 | intron-variant, stop-gained | CADPS2, RNF133 | GRCh38.p7 | 7:122698639 | CTGAGTACTTTGATC[A/G]GCTGAAAATGGTATT | 93664 |
rs145560887 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122484253 | TTGGAGGACTTGGAC[C/T]ACCTAACTGTAAGAT | 93664 |
rs145569273 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122857027 | TAAGGTTTTTGCAGA[C/T]ATTCATCATGGCACA | 93664 |
rs145569378 | in-del | -/TT | 0.0314385 | 0.121371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122642926 | GAGTGAATTGCACTC[-/TT]TTGTTTTCTTATAAT | 93664 |
rs145572891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122763360 | GAGAGTGCTGAATCC[C/T]ACTCCACGACAATAA | 93664 |
rs145574210 | in-del | -/T | 0.122411 | 0.214991 | intron-variant | CADPS2 | GRCh38.p7 | 7:122452083 | CCTGTGAAATCAATG[-/T]TGAGTTTCATCAGAA | 93664 |
rs145580617 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122739232 | GGCAATGGAAATGTA[G/T]GCAAAGAATGACAAT | 93664 |
rs145587897 | snp | A/G | 0.00578766 | 0.0534854 | intron-variant, synonymous-codon | CADPS2, RNF133 | GRCh38.p7 | 7:122698394 | CCCCACCTCAACCAC[A/G]GCTGTAATGAGAACT | 93664 |
rs145596231 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122637827 | TAAGTTGAGTATAGT[C/T]AGTTGGCTCCATTTC | 93664 |
rs145600504 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122801039 | CTTCTTACCTTGGGG[C/T]AATTAAGAAAAACAC | 93664 |
rs145606158 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122394956 | GGTGAAGAGGTAGAA[G/T]CTGGGGAAAAGTTAG | 93664 |
rs145610877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122757590 | GTCATAATTTTAGGC[A/G]GCCCTGACACCCATG | 93664 |
rs145620054 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | CADPS2 | GRCh38.p7 | 7:122404286 | GCTGAGAATGATGGT[C/T]TCCAGCTTCATCCAT | 93664 |
rs145620175 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122545032 | TAAAAAGTAAAGAGA[C/T]GGAATAGGGAACACA | 93664 |
rs145621057 | snp | C/T | 0.179425 | 0.239831 | intron-variant | CADPS2 | GRCh38.p7 | 7:122679581 | GTTGCCCTTAAAGCA[C/T]GTGATCTCTGTGACC | 93664 |
rs145621982 | in-del | -/TACCCTAATCAGAG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122648575 | GTGTTAAAACAAAAA[-/TACCCTAATCAGAG]AAGCCACATCATACT | 93664 |
rs145623486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122629133 | TGTGTAGAGGAGAAA[A/G]TGTTAAAATTATGCT | 93664 |
rs145633213 | in-del | -/TTTA | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122476705 | AAACCCATTAAAATT[-/TTTA]TTTAAGAAAATCAAC | 93664 |
rs145635022 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122336470 | ACAAGGCACTAGAGA[C/G]CAGTTGAAATGCAAG | 93664 |
rs145644254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539579 | TAACAGTATTCAATG[C/T]TCTGTGCTCCAAATC | 93664 |
rs145645652 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122396030 | GGTCGGGCTAGTCTC[A/G]AACTCCCGACCTCAG | 93664 |
rs145651847 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122624616 | TTTTTGCTACAAATT[A/T]GAGCAGATTCAGTTA | 93664 |
rs145653607 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122491583 | AGCTCAGAGATTCAA[G/T]CACCTTTCGTTTGTC | 93664 |
rs145663581 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122740966 | CATATCCTTGGAATC[A/T]GCAATTCCACTTTGA | 93664 |
rs145671569 | in-del | -/A | 0.0410537 | 0.137264 | intron-variant | CADPS2 | GRCh38.p7 | 7:122486257 | TATGAGACATCTGGG[-/A]AAAGTAAATTGAAAA | 93664 |
rs145687754 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122675210 | TGTGGGACCTGTCTG[C/T]GACTCACACAAAACG | 93664 |
rs145690748 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122540932 | GAAATAATTTTTAAC[C/T]CATTTATTCATAATA | 93664 |
rs145697438 | in-del | -/ATTCC | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122403781 | CATTGTAGATAAGTA[-/ATTCC]ATTCATTGTAGATGA | 93664 |
rs145698138 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122343020 | ATCTGTTGCTTAAGA[C/T]ACACATTCTACTTTG | 93664 |
rs145701128 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122625876 | TATTATATCTACCTA[C/G]ATATTGGTCTAGATA | 93664 |
rs145732114 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122505328 | TGCTATAAGTATTGT[A/G]TCTCTAGCTAGCTTT | 93664 |
rs145736125 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122551126 | GCATTTTACCTTCTG[C/G]TTTAAAAAAATAGTC | 93664 |
rs145741337 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122634657 | ACTTTTACATGTCAA[C/T]TTCATTCAGTTCTTT | 93664 |
rs145752719 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122831395 | AAACATTCTAGTCTT[A/C]AAAAACCATCAGTAT | 93664 |
rs145758618 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122365654 | TGAGGGTGTCGGGTT[G/T]GAATGAAACACTGTA | 93664 |
rs145764643 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122781874 | TTCAAAAATAACCAC[A/G]GTGAAATATGAAATA | 93664 |
rs145770796 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122659880 | AAAGAGAAAAAAAAA[-/A]TCTAACAGATAATTC | 93664 |
rs145789671 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122800655 | ATAATAGAGCTAGTA[C/T]AGTAAAATAAGAATT | 93664 |
rs145798008 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122879675 | ATTGACAAAGACAGG[C/T]TTTAAATTTTCAGGC | 93664 |
rs145809915 | in-del | -/AGT | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122538138 | AATCCCACTTATACA[-/AGT]AATTCAGTAAAAAAA | 93664 |
rs145813612 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | CADPS2 | GRCh38.p7 | 7:122635603 | GTCCTTACAAAGGAC[A/G]TGAACTCATCATTTT | 93664 |
rs145831347 | snp | A/G | 0.00463315 | 0.0479073 | intron-variant | CADPS2 | GRCh38.p7 | 7:122414111 | TGGAAGCATTGCAGA[A/G]TAGAACAATTGCCAT | 93664 |
rs145831752 | in-del | -/TCTCTCTCCCTGTCTGTT | 0.487871 | 0.076925 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539753 | CCCTCTCTCTCTGTC[-/TCTCTCTCCCTGTCTGTT]TCTCTCTGTCTCTGT | 93664 |
rs145838115 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122510932 | AAACTTGTCAGAATA[C/G]TCGCATGGATTCTCA | 93664 |
rs145851807 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122330568 | AACCAGACCCCCAGG[C/T]ACAAGCATTTTGCAA | 93664 |
rs145851991 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122439670 | ACTTTATCATTCTCT[A/C]TCTATCAAATTCAAT | 93664 |
rs145853657 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122425138 | GGAGTGCACCACCAC[A/G]CCCAACTAATTAAGT | 93664 |
rs145855264 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122867878 | GCTTTTGAGATATAG[A/T]CCTGCAATCTCACAT | 93664 |
rs145861426 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122748648 | GCTTTCTTTCTTGAC[C/T]AGGTATTACATGGAT | 93664 |
rs145870733 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | CADPS2 | GRCh38.p7 | 7:122645312 | ACACATATGTACATG[C/T]GTGTATACATGTACA | 93664 |
rs145873496 | snp | C/G | 0.0314385 | 0.121371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122836269 | TGCCCTAAAAGAGCT[C/G]CTGAAGGAAGCACTA | 93664 |
rs145883288 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122410910 | ATTATTTCAGGTAGA[C/T]TGTACAATTATCCTT | 93664 |
rs145885025 | in-del | -/AGAA | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122826573 | AAATGAATATAAAAT[-/AGAA]AGCCTCAGCAAAGGA | 93664 |
rs145893954 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122872372 | TTAAAAACAATGAGA[C/T]TCATTATAGGAACCT | 93664 |
rs145899620 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122735358 | TACATATGGCATGTT[A/T]CAAACCTGATCACTA | 93664 |
rs145899999 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122785589 | CCTTCAGAAATAGCA[A/G]TGGAAAGCCTTTTTG | 93664 |
rs145904153 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122659747 | GGAAAAACTCTTGAA[C/G]GAAGCCATAAGGGGG | 93664 |
rs145914251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122480371 | GATTTATACTTCATT[C/T]TAAAGCACTGGGTTT | 93664 |
rs145917241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122572608 | AGGAGTATATACTAC[C/T]CAATATTTCACTGTG | 93664 |
rs145919812 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122414548 | AGCTGTGTTACCAGC[C/T]TAGAAAAGAACCTCC | 93664 |
rs145923714 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122411354 | GCCTCCCAAGTATCT[C/G]GGATTACAGGTGCCC | 93664 |
rs145923724 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122356910 | CCAGCCATTTCTCCA[A/T]TGAGCCCTGGTTCAT | 93664 |
rs145923809 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122865246 | GCCTGAGACTCTCAC[C/T]AGTTGCCAGCGCCTT | 93664 |
rs145926375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122690079 | ACAGTGCCGATCCAA[C/T]AGTTAGAGACATTGG | 93664 |
rs145944105 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122361573 | AAAGATAATGTGTCA[C/T]AGGAATCTAGTCACT | 93664 |
rs145944394 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122861363 | TAATTAGTGATATTG[A/G]GCATTTTTTCATATA | 93664 |
rs145965939 | snp | C/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122406132 | TGTCCATGGAAAGTA[C/T]AATATTACAAATGAT | 93664 |
rs145969989 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CADPS2 | GRCh38.p7 | 7:122503536 | CAAAATAGTTTAATA[C/T]TAATATGATTGCTCT | 93664 |
rs145970611 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122731713 | AAAAAGATGAAAGTG[C/T]AGCAGAATCAAACAA | 93664 |
rs145991031 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122750777 | ACGAAAGACCTACCC[C/T]ACACCTACTATTTCA | 93664 |
rs145992267 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122553688 | CCACCCTGATGTTAG[C/T]GATTGGGCCCTAATG | 93664 |
rs145992789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122674369 | GCAAGGGCTGCTAGC[A/G]CTTTGTCACCTTTCA | 93664 |
rs145993346 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122325144 | TGATCCTAATAAATA[C/T]GAAGTAATTGTATTA | 93664 |
rs145993526 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122421118 | GATGTGGGAAGAAGA[C/T]CAGTGAGATACCTTC | 93664 |
rs145995080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122636664 | AAAGACAAGGTTTCA[C/T]CATGTTGACCAGACT | 93664 |
rs146005316 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, utr-variant-5-prime | CADPS2 | GRCh38.p7 | 7:122885724 | CCTGCCGGGTGCAAC[C/T]GCGGCGCGGCCGGCG | 93664 |
rs146006837 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | CADPS2 | GRCh38.p7 | 7:122484977 | TTATTAGTAGATCTA[C/T]CACGGTCATCTGTGG | 93664 |
rs146010105 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122804187 | TAGTTTCCTTTCCCC[A/G]CATCAGTGCCAAGGC | 93664 |
rs146011839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122498460 | TTATTTAATGCCTTT[A/G]TTCAAATCCTATCAG | 93664 |
rs146014296 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122640169 | CCCTCACAGTCCACA[C/T]CCAATCCACCTAGAG | 93664 |
rs146018541 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122576412 | CCTTTCAGTGGAGCT[A/T]TGTCATACCTGTAGA | 93664 |
rs146046566 | snp | C/G | 0.00993419 | 0.0697739 | upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122887468 | GTTCTGGCCTCAAGT[C/G]GGCGTCTTGTAGCTG | 93664 |
rs146048433 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122379636 | GGTTTGAAAATTTTC[C/T]CATGTGCACTGTTGA | 93664 |
rs146057378 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122686517 | TGGTGAACCAGATTG[C/T]TGCCCCCTCCTCAAG | 93664 |
rs146057450 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122733564 | CAAGTAGCTAACTAG[A/G]TTTACATTCAAATTG | 93664 |
rs146061920 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122699200 | CAAGACCCAGCAGCC[-/A]ATTAGATAAGAGCTT | 93664 |
rs146064329 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122882145 | TCCCCAAATGTTCTT[C/T]TCCAGATCAATTTTA | 93664 |
rs146090923 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | CADPS2 | GRCh38.p7 | 7:122428331 | TCTTTAACACCATGC[A/C]CTCAAGTAAAAGAAA | 93664 |
rs146093331 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122531599 | TCTCAGTTGAGTCTC[A/G]ATCAGTTTTTTCTAA | 93664 |
rs146114687 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122691523 | TGTGTAAGCCTCACC[A/G]TGCAACCCCAGGCAA | 93664 |
rs146115437 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122574979 | AATATTAGAAAAAAC[G/T]GTCACTCTGTAACTT | 93664 |
rs146131201 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122823664 | ACTATGAATGGAGAA[C/T]GGATGCAATTAGAAG | 93664 |
rs146134044 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122423189 | GCCATAGCAACCTGT[A/G]GTAAGTTACATGGTG | 93664 |
rs146134828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122688679 | AGTCCCTATATAGTG[C/T]CAGCAGGGCAATGAT | 93664 |
rs146135256 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122736531 | ATTTCTTTAGGAAGC[A/G]AAGAGAATTCAATTC | 93664 |
rs146135921 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122579315 | ACAAAAAAGCACCTG[A/C]CAACAAAGAATTACC | 93664 |
rs146174044 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122620724 | ATGATACCTAATAAT[A/G]TGCATTAGAACTGGC | 93664 |
rs146210679 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | CADPS2 | GRCh38.p7 | 7:122860780 | ACTATTATACTCTCT[A/T]CTTCTATGAGATCAA | 93664 |
rs146210855 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122361783 | TTGAATATAAAAGAA[C/G]AGATAATGGGCCAGG | 93664 |
rs146212895 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122771868 | AGAGTGTCAACTGAA[A/C]AGTGAGGTAAGGTGA | 93664 |
rs146213030 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122454045 | TAAGAAGCAGCCTTC[C/T]ATATCTAAATTATTG | 93664 |
rs146234501 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122504003 | AACCATATTAAGGTA[C/T]TTCAACTGGAAGTGA | 93664 |
rs146235787 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122715065 | TCCACAACTGTGAGA[G/T]AATAAGTTTCTGTTG | 93664 |
rs146237437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122596917 | GAGCTGGCTGGAAGA[C/T]TGGGTGTCCAGTGAG | 93664 |
rs146252225 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122449566 | GGCTCAAGCAACCTT[C/T]CCTCCTAAAGTGCTG | 93664 |
rs146253616 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122756625 | TCCCAAGGGTTGGGC[A/G]CGGTGGCACACGCCT | 93664 |
rs146254152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122710965 | TCCCTGACAAAATGT[C/T]GATTTTCAAGTACTT | 93664 |
rs146259360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122636885 | TTTCTTAAATTTGTA[C/T]GTCCAACTCTCTAGT | 93664 |
rs146278617 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | CADPS2 | GRCh38.p7 | 7:122640639 | AAATAAAAATAAAAA[A/T]AAATATTGTTGGCTG | 93664 |
rs146288511 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122326467 | TAAGGGACACAGTGA[G/T]TCAGAGCTAGGTTTA | 93664 |
rs146307033 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122333408 | GAGTGTCCTAAGGAC[A/C/G]GGAGTAGACAGCTAC | 93664 |
rs146309939 | snp | C/T | 0.117886 | 0.21224 | intron-variant | CADPS2 | GRCh38.p7 | 7:122839059 | GTCACCAAAACAGCA[C/T]GGTGCTGGTACCAAA | 93664 |
rs146313340 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122765437 | AAATAAAAATTAATG[A/C]GTACATGGATAAATG | 93664 |
rs146329610 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122385005 | AACGGATAAACCCAG[A/T]ATGAATGGAAGATGA | 93664 |
rs146331885 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122482473 | CAAAATGTCAATAGT[A/G]TTGAAATTGAGAAAC | 93664 |
rs146343444 | in-del | -/TTTATATATATATATATATATATATATATATATATA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122323872 | TATACATATGTATAT[lengthTooLong]TATATATATATATAT | 93664 |
rs146355483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122532074 | AAACAAAATACTGTT[A/G]GCCTGTTAGCATTAT | 93664 |
rs146356897 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122361223 | GGCTGGAAATAATAC[-/A]CTTTTTTTTTTTTTT | 93664 |
rs146358537 | snp | C/G | 0.0729998 | 0.176553 | intron-variant | CADPS2 | GRCh38.p7 | 7:122657090 | CCATTTCTTGTTTTT[C/G]TCAGGTTTGTCAAAG | 93664 |
rs146359121 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122618153 | ACATTTAACATTATT[A/G]AACAGCTTAGCGTTT | 93664 |
rs146373335 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122864317 | CATACACCAAAAATA[C/T]AAAAAAAATAAAATT | 93664 |
rs146373964 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | CADPS2 | GRCh38.p7 | 7:122777546 | CCACCCAAATGTCAT[C/G]TTGAACTGTAGTTCT | 93664 |
rs146375051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122537202 | TTCAAGAAGCATGTA[C/T]ACAACTATTTATCAA | 93664 |
rs146375140 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122473571 | AAGCATTTTGGATAA[A/G]GGATAGTCAACCTGT | 93664 |
rs146375186 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122727836 | ATTTAAAATGCCATC[C/G]TTAGAATATAAGAAA | 93664 |
rs146377532 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122651943 | GCTTACCTACCTCTG[G/T]TAATATCTCAAATAC | 93664 |
rs146378130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122623491 | CTTATTATTTATTAT[C/T]GATTAAAGATTCCAG | 93664 |
rs146409113 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817450 | ATTTTCTGGGAGAGA[C/T]AAAGGCGACACGTTT | 93664 |
rs146411575 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122728072 | TTTTCCAGGGCATTA[C/T]TGCAAAGTTTAAAAG | 93664 |
rs146412398 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122681303 | AAGAGCTCTCCGGTC[C/T]GTGCCTCCAAGATGA | 93664 |
rs146419608 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122615807 | AGATTACTATTATTG[C/T]CTGTAAAAGAGTTTA | 93664 |
rs146430822 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122725112 | AATGTAATGTGATAT[A/G]AAAATATATGTGTTT | 93664 |
rs146435283 | snp | G/T | 0.000211812 | 0.0102889 | intron-variant, synonymous-codon | CADPS2, RNF133 | GRCh38.p7 | 7:122697815 | ATGAACATCTTCCAC[G/T]ACTGAATGAGGCTGG | 93664 |
rs146435415 | snp | C/G | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122818674 | ATCTTTTTATCACCT[C/G]CCCTCCTCACACCTG | 93664 |
rs146436265 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | CADPS2 | GRCh38.p7 | 7:122468449 | TTAGGAATATAATTA[C/T]ATACACATTGAAATA | 93664 |
rs146454498 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122685245 | TTAAGGAAGAGAAAC[C/T]AGGCTCTCTGAAGGC | 93664 |
rs146461676 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122610906 | TTCTCTCGGCCACTG[A/G]AGTGACATGGTAGGA | 93664 |
rs146475768 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122397940 | CACCTATTTTTCAGA[C/T]AAAAAAATAACTTTT | 93664 |
rs146479996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122493588 | CAGTGTGGGTGACAG[A/G]ATGAAAACTGGTGTG | 93664 |
rs146493548 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122345008 | GATTTCAGTAAATAG[C/G]TCACCAAGACAAAAA | 93664 |
rs146494033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122403971 | TCTTACCTAATTGCT[C/T]GATGGTGAACATTAA | 93664 |
rs146504351 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122359647 | AACATAAAATCTCCC[C/G]TTAATTCTCCCTTTC | 93664 |
rs146512970 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122856181 | CCAACATCCCACTCC[C/T]TGTGTTCTTGTGAAG | 93664 |
rs146517470 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122395291 | ACACAGAAGGAAATA[C/T]AACAGATTTTTTTTT | 93664 |
rs146521200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122549929 | GAGCAAATACTACCT[C/T]GACGCAGCTAAGATT | 93664 |
rs146523603 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122634343 | AATTACTGATTCAAT[G/T]TCAGCATTTGTTACT | 93664 |
rs146531356 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122851266 | TACAGTGCAGTCCCC[A/T]GGGATGTTCAACTGG | 93664 |
rs146532818 | snp | C/T | 0.030278 | 0.119257 | intron-variant | CADPS2 | GRCh38.p7 | 7:122835412 | GCAGCTCCTCGCCAG[C/T]AATGGAACAAAGCTG | 93664 |
rs146535275 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122748022 | CTAGGATGCAGATTT[A/C]TTCAACGCAGATGCC | 93664 |
rs146536276 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122700901 | GAACACTTTTCCTTA[A/C]ATATCCAAAGTACTA | 93664 |
rs146544447 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122634524 | TATTCTGTAAATCCA[C/T]CTTTGTCATTTCTGG | 93664 |
rs146554847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122743897 | CAGAAAAATAGGGGG[C/T]TCCAGCTACGTCTCA | 93664 |
rs146560327 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122494312 | ACGTATCTCAAGGAA[A/G]CAAATGGAGAAGTAC | 93664 |
rs146566929 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122770537 | CTCCCCTGAACTCAG[C/T]ACTTATGGGAGAATA | 93664 |
rs146571999 | in-del | -/AT | 0.348134 | 0.229934 | intron-variant | CADPS2 | GRCh38.p7 | 7:122797681 | GGGAATGATGGACAC[-/AT]AGACGGGAACAACAG | 93664 |
rs146586114 | snp | C/T | 0.000399281 | 0.0141238 | missense | CADPS2 | GRCh38.p7 | 7:122629253 | AATAATTTACCTTTG[C/T]CATTTTATCTGCCAA | 93664 |
rs146594579 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122322469 | GTTATTGACACTTGG[A/G]TGTTCCCTGTGGCTT | 93664 |
rs146598562 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122418896 | AAAAAAATTGTGCAT[A/T]GTAAAATCTACAAAC | 93664 |
rs146622377 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | CADPS2 | GRCh38.p7 | 7:122618883 | GGACACATAACTCCT[A/G]CTTAAAATACTGTGG | 93664 |
rs146628658 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | CADPS2 | GRCh38.p7 | 7:122876371 | AATTTTATATTTATT[C/T]TTTCTTTTGAGACAG | 93664 |
rs146639832 | snp | C/G | 0.021333 | 0.101051 | intron-variant | CADPS2 | GRCh38.p7 | 7:122571292 | ACCATAATGAAATAA[C/G]AATATATACCTATTA | 93664 |
rs146643868 | in-del | -/AATA | 0.0984431 | 0.198823 | intron-variant | CADPS2 | GRCh38.p7 | 7:122884617 | TAAGGATTCCCAGAG[-/AATA]AATGATTCCAAAATA | 93664 |
rs146647373 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122872972 | ATAGTAAGCACAAAC[A/G]TAAGGAAGGCGAAGG | 93664 |
rs146651510 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122855731 | ACTGCTTCTACATCT[A/G]TCTCGAGCCCTGACA | 93664 |
rs146653718 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122767591 | TAGACCAACAAAGGC[C/G]CTAATTCTGCTCAGC | 93664 |
rs146654434 | in-del | -/ACA | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122710344 | CAGAGAAAAACGATG[-/ACA]ACAACATGAGCATAG | 93664 |
rs146656120 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122645432 | GTATATGTGTGTATA[C/T]ATGTATATATACACA | 93664 |
rs146672807 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122762260 | AATCAGAGAACAAGC[C/T]GGGCGGCAGTCCAAC | 93664 |
rs146680247 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122519842 | GAGAAAACATTTTTT[A/T]AAATGGTATTTGCCT | 93664 |
rs146684063 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122501317 | TTGATTATGTAGCAA[G/T]GATTTGAAGATATTA | 93664 |
rs146695120 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122724437 | TTATAATTATCACAA[A/C]GCAGTACACATGATA | 93664 |
rs146697039 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122648029 | AAGGAGTCTGCCCTT[A/G]TCAAAGTCAATAGTG | 93664 |
rs146698763 | in-del | -/T | 0.211819 | 0.247067 | intron-variant | CADPS2 | GRCh38.p7 | 7:122647216 | TCTTTTTTACTACAG[-/T]TTTTTTTTCCAGTGG | 93664 |
rs146713138 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122353010 | TTTATTGCAACAGTG[C/T]TTTACAATTCAAAGC | 93664 |
rs146716673 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122446019 | GTGACAATTTTGAAC[A/G]TAAGAAGTGAGAGCA | 93664 |
rs146732579 | in-del | -/TTTA | 0.273049 | 0.248935 | intron-variant | CADPS2 | GRCh38.p7 | 7:122637047 | TATTTTTTTAAATTG[-/TTTA]TTTATTTTTTTCTTT | 93664 |
rs146734990 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122357074 | ATCTAAAAATACTGT[C/T]AAATGTAACCAGCTC | 93664 |
rs146758499 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | CADPS2 | GRCh38.p7 | 7:122499494 | GCACTATATTTTATT[C/T]GGCATTTCTAGGTAT | 93664 |
rs146759758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122439598 | TTTTTAAAGGCTACT[C/T]TTTGATGACATTTTA | 93664 |
rs146761580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122590274 | TGGCAAAAAGACAGA[C/T]ATACAAACCAATGGA | 93664 |
rs146770990 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122814518 | AAAGAAAAAAGATAA[C/T]TATTCATGACATGTC | 93664 |
rs146773984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122789515 | ATTCACTATAAGCAT[C/T]ACACTCTAACCTCAA | 93664 |
rs146776406 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122711782 | CTCAGCCCCCTGAAT[A/G]GCTGGGATTACAGGC | 93664 |
rs146776498 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122662702 | GTATGTATAACTAGA[A/G]TAACAACTGAAGAGA | 93664 |
rs146793432 | in-del | -/AA | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122516900 | TTTTATTGTTTGAGT[-/AA]AGTTTATTGGTATAG | 93664 |
rs146796142 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122707035 | CAGAGGAAGGGTGAA[G/T]ATTTGAATGCTGTGT | 93664 |
rs146799724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122355281 | GAATCAATTTATTTA[C/T]TGCTTTAAAAACATT | 93664 |
rs146801713 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122544601 | CCTGAAACCCAGGTC[A/T]GCACAACTAGGCTGA | 93664 |
rs146813210 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | CADPS2 | GRCh38.p7 | 7:122321612 | TCCCACCTCAGCCTC[C/T]CGAGTAGCTGGGATT | 93664 |
rs146817595 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122666660 | TAACACAATTTTAAG[C/G]AACATCGGTAGAGGC | 93664 |
rs146817950 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122447846 | GTGTGAGCCACTGCA[C/T]CCAGCCAGTTTCAGG | 93664 |
rs146817959 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | CADPS2 | GRCh38.p7 | 7:122506209 | ATTTGTTTTCATTTA[C/T]GAGCCTACTTGTGTA | 93664 |
rs146837037 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122600262 | GGAGTCAAAGCAACA[A/C]AGCTAAGCTGAGATT | 93664 |
rs146837854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122375492 | GAGAAAAGGATGGTT[C/T]CTTCAATAAATAGTG | 93664 |
rs146839204 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122467729 | TTGTGTTGCTGCTTC[A/C]GTTTCTCCACCCTCA | 93664 |
rs146856904 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122381245 | CCACTCTTGTTTCAC[A/G]TCCTTCTTGCTCCAG | 93664 |
rs146863034 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122708783 | CTTATTCAGTCTACC[G/T]ATTTAGAAGATAGAA | 93664 |
rs146875244 | in-del | -/ACTA | 0.124144 | 0.21601 | intron-variant | CADPS2 | GRCh38.p7 | 7:122791635 | TTGCTATTTAATAAC[-/ACTA]ACCATGGCAACACAG | 93664 |
rs146882046 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122462729 | TCACCTACATATCAT[G/T]CAAAAATCATTATTA | 93664 |
rs146882125 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122525170 | CTTTAAAAAGTTTTC[C/T]TTAAAATTTTGATCA | 93664 |
rs146886943 | in-del | -/TC | 0.0158469 | 0.0875917 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122545208 | AAAAGACTCAATAGT[-/TC]TCTCAAAAATCAAGG | 93664 |
rs146901939 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122832708 | TGCTGGTTACAAATA[C/T]AAACTGAAGTAATTC | 93664 |
rs146906158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122589061 | AATGAGCTGTAGTAT[C/T]CTTTAGTTTCATTAA | 93664 |
rs146921647 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122842148 | CAGGAACACGGCCCA[C/G]TTCAGATGCCCCTGC | 93664 |
rs146922328 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122786657 | TTTTTACTACTGTTA[A/C/T]GAGTTTCGTGTTTAA | 93664 |
rs146933913 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122329410 | CTCTGCTCTTGGGGC[C/T]GGGGAGCACTAACAA | 93664 |
rs146944432 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122668780 | TCACTTTTGACAGAC[A/C]AGATTTACTGGAGTG | 93664 |
rs146944439 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122718599 | CCGTTGTTAACAGTC[C/T]AGTGAGTGTAACAAA | 93664 |
rs146951206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122382882 | ATTAATTCAGCCACT[A/G]TGGAAAGCAGTTTGA | 93664 |
rs146958640 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122793324 | TCCATGCTGGGTGCA[C/T]ATACATTTAAGATAG | 93664 |
rs146960797 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122714303 | TGTAAGTAGCAGTCT[A/G]TACCTACAAGAATAC | 93664 |
rs146967562 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CADPS2 | GRCh38.p7 | 7:122324488 | TACTGGGTTCCACCC[C/T]CGGAATTTCTGATTC | 93664 |
rs146981093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122653582 | TTGAGTTTCTCTTTA[C/T]TGCACTTTGCAGATA | 93664 |
rs146987746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122377369 | ATGCAGAGATGACAT[A/G]CAGCCCCATCTGCCT | 93664 |
rs146990455 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122534130 | ATTTAGGAGTCTGAA[C/T]ATTTGCTGATCTGAA | 93664 |
rs146990834 | in-del | -/T/TT | 0.069206 | 0.173816 | intron-variant | CADPS2 | GRCh38.p7 | 7:122385295 | GGTAATATAAATACA[-/T/TT]TTTTTTTTTCTGCTG | 93664 |
rs147026441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122816123 | AGATCTTATCCTTTC[C/T]TCCTATTTTTTTAAC | 93664 |
rs147027715 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122863224 | AATTTACCTGGGTGT[C/T]TTCTACATATCTGCG | 93664 |
rs147039302 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122358860 | GGTATAGTATGTTCT[A/G/T]CTCCAGGGGGCAACT | 93664 |
rs147042985 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122858010 | TCGTGAAGAGCGAAA[C/G]AACAAAGCTTCCACA | 93664 |
rs147047273 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122617741 | ATCAATGAAAGAATT[C/G]AGTCTAAAAAATCAA | 93664 |
rs147060558 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122500559 | AGTAAACATCCCCTC[A/G]TGCAAGTAGGCACCC | 93664 |
rs147063729 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817924 | CAATCCCTTATTTCC[A/G]TGCCCCAACCCCTTA | 93664 |
rs147064835 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122729290 | ACACTTAGGTTGATT[C/T]CACATCTTTGCTATT | 93664 |
rs147079671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122551403 | GAGAATTCAAATAGG[C/T]CTAAGAAACTTAGAG | 93664 |
rs147083618 | in-del | -/ATAAG | 0.487995 | 0.0765403 | intron-variant | CADPS2 | GRCh38.p7 | 7:122490713 | ATAAAATTCTTTCAC[-/ATAAG]ATAATATTTTGCATT | 93664 |
rs147085183 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122672738 | CACCTGTGGAATTAT[C/G]GACCAGTGACTTTCT | 93664 |
rs147094273 | snp | C/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122401051 | CACTCTGGGCTCTAT[C/T]ATGGCTAATTTGACT | 93664 |
rs147095223 | in-del | -/ATAAT | 0.0410537 | 0.137264 | intron-variant | CADPS2 | GRCh38.p7 | 7:122454448 | ATATTTTGATAGAAA[-/ATAAT]AACGAGCAATAGAAA | 93664 |
rs147095667 | snp | A/C | 0.000127337 | 0.00797824 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554712 | GAAAAAAAAACCCAC[A/C]TTTAAACGCATGATA | 93664 |
rs147133364 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | CADPS2 | GRCh38.p7 | 7:122745358 | TCAAAGAAGTTAAGG[A/T]TCTTACTTAACCTCG | 93664 |
rs147135397 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122632457 | TGCATTTCTCTGATG[A/C]TTAGTGATGTTGAGC | 93664 |
rs147139068 | in-del | -/ATC | 0.0437281 | 0.141251 | intron-variant | CADPS2 | GRCh38.p7 | 7:122344355 | TGTCACAAGCAAAGT[-/ATC]ATTTCCTTTGAACTG | 93664 |
rs147149730 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122492323 | CAGCCAGTGACAACA[C/T]TGCCAAGATCTGGTC | 93664 |
rs147152030 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122585234 | ATATTTATCCTTGTA[A/T]CCTGGAAAGTTGGGA | 93664 |
rs147169344 | snp | C/G/T | 9.9373e-05 | 0.00704824 | intron-variant, synonymous-codon | CADPS2, RNF148 | GRCh38.p7 | 7:122702295 | GTTGCTTATCATCAC[C/G/T]GCGACTATATTTTCC | 93664 |
rs147171378 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122627792 | CATCTCTCCAGGTTC[C/T]TTATTAGCTTTAGGT | 93664 |
rs147181280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122869922 | AAATGTTTTATGGTA[A/G]CCTCATGGTAACCAC | 93664 |
rs147182912 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122417091 | CTTAAAGGGCATTTT[C/T]TTTTCCTACAATAGT | 93664 |
rs147217313 | snp | A/G | 0.000767571 | 0.0195754 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122471383 | AAAATACCTGTTGCC[A/G]TGCACATGAGAGGCA | 93664 |
rs147218813 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122737870 | CTGAAAAGACAGAAC[A/G]TACCCTAAGAAAGAT | 93664 |
rs147220439 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122567683 | TAACAATAACTCAAA[G/T]GATGGGAGGGAAGAA | 93664 |
rs147239936 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122645226 | TAAGTATATATATAC[G/T]CTAAGTATATATATA | 93664 |
rs147239954 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | CADPS2 | GRCh38.p7 | 7:122686874 | ATTTTTAGTAGAGAC[A/G]GGGTTTTACCATGTT | 93664 |
rs147241900 | in-del | -/TA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122706580 | TTAACAGCGAATATG[-/TA]TATATATATATATCA | 93664 |
rs147253900 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122761326 | CCAGGCCAATACTCA[C/T]CTCTGAGGAATCAAA | 93664 |
rs147256079 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122516567 | TGAAGAAGGAATGAA[A/G]ATAAAAATGTTCATC | 93664 |
rs147256443 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122684215 | CCTGTGGTTAAATTG[A/C]TATCATTATATGTCG | 93664 |
rs147287270 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122347953 | GAACAATTTTCAATA[C/T]ACAATAGCAAGTTAA | 93664 |
rs147287689 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122813038 | GACACAGCAGGAAAA[G/T]CCTCAATAACAGGAC | 93664 |
rs147287975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122444097 | TGTGGGTCTGATTTC[C/T]TTCACTTAGCATAGT | 93664 |
rs147313201 | in-del | -/AG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122688767 | ACATGGTTGTGGTAA[-/AG]CGGGGAGTTATACAC | 93664 |
rs147324121 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122343128 | TTTAGTATCCCCTCA[A/T]ACATGTTATTCCTGA | 93664 |
rs147324526 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122435472 | ATCATCTCACACCTG[C/T]TGGGACGACTATTAT | 93664 |
rs147324569 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122757891 | TGGATGTTTTTCTGC[A/G]TATATTCACATAGCA | 93664 |
rs147325194 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122496020 | TATACCATTTTCCAC[A/G]ATCAATTTTGCCAGA | 93664 |
rs147345913 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122709914 | GACTGTTGTGGGGTT[A/G]GGGGAGAGGGAAGGG | 93664 |
rs147346247 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122660508 | AAGTGGTAAAAGCTA[A/C]AAAGATTTTAAAATT | 93664 |
rs147346629 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122589640 | ACACGTCGTTTACTA[C/T]GATCCAAACTATAAG | 93664 |
rs147347293 | in-del | -/GAAA | 0.0189856 | 0.0955633 | intron-variant | CADPS2 | GRCh38.p7 | 7:122494858 | CTAAGGTTTACAAAT[-/GAAA]GTCAGTTGCTCCCAT | 93664 |
rs147359770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122444911 | GTTTTCTAGGTCTAC[C/T]TATTTTGAGTTAACT | 93664 |
rs147359939 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122783901 | ACCATATCTATTACC[A/G]ATGTTATGCAAACTC | 93664 |
rs147362816 | snp | C/T | 0.00275622 | 0.0370204 | intron-variant, synonymous-codon | CADPS2, RNF148 | GRCh38.p7 | 7:122702724 | AACAGAACTATGCGT[C/T]GAAGGGGTAATTCTA | 93664 |
rs147366485 | in-del | -/TCAACTCAATT | 0.0693013 | 0.172766 | intron-variant | CADPS2 | GRCh38.p7 | 7:122343745 | ATAATGGGAATAACA[-/TCAACTCAATT]TCCCTCTTCTGTTCA | 93664 |
rs147372111 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | CADPS2 | GRCh38.p7 | 7:122318526 | TTGGGGATGGTGCCA[C/T]TGGAGAGTTTGGGAT | 93664 |
rs147382125 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122664785 | AAAAATTCAAGTCAA[A/C]TTTTTTTTCTTTTTT | 93664 |
rs147382543 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122585572 | ATATTTAAACCCTGT[C/G]GGTAATTAATACCAG | 93664 |
rs147391780 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122373595 | CTGCTGAAGTCAATC[A/G]GTAAATAGTGGAAAA | 93664 |
rs147394134 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122830305 | GGATTCTATTTTAAG[A/G]GAAATAAGGACAAAA | 93664 |
rs147395440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122465631 | GGAACAGTTTCATCC[C/T]AAAACCATCCCCATC | 93664 |
rs147410748 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122574443 | AGAGTGAGACCCTGT[C/T]TTAAAAAAAAAAAAA | 93664 |
rs147428696 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122833647 | GTGATCTGCCCACCT[C/T]GGCCTCCGAAAGTGC | 93664 |
rs147430140 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122778600 | CTTTGCTGTGTGCCA[C/G]CTAGGGACTTGGTGC | 93664 |
rs147431896 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122521880 | TAGTTTCATCTCAGT[C/T]AAATCCAAGTTAAGC | 93664 |
rs147443586 | in-del | -/TT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122367711 | ACCATGCCCAGCTAA[-/TT]TTTTTTTTTTTTTTT | 93664 |
rs147450205 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122726199 | AATATTCTTGACAAC[C/T]GTAAGGGGGACTATG | 93664 |
rs147450545 | snp | A/G | 0.180383 | 0.240111 | intron-variant | CADPS2 | GRCh38.p7 | 7:122679148 | GGCTGCCTGTGGGCC[A/G]GGCAGGACAGAGCCA | 93664 |
rs147451741 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122557995 | CCAATACCTAGGAAA[C/G/T]GAAAGAAATCAGAGC | 93664 |
rs147451874 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122614332 | CCTCTGTATCTCCCT[A/C]TCCTGCCTGCTCTAA | 93664 |
rs147459527 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122808480 | AGATAACAGTTTCAT[C/T]ACCTTCTGCTGGAGT | 93664 |
rs147465328 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122811771 | ATAGTTACCTAAGTA[C/T]GTCAACATATTTCTT | 93664 |
rs147465697 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122466099 | AGAAGGCTCTAAAGG[C/T]ATGAAGTTTAAGAAA | 93664 |
rs147486322 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122683142 | GAAGTGGTTCTTGGC[A/G]GGATGAGAGTTGGAA | 93664 |
rs147496707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122847658 | TACTAAGCTTATGGC[A/G]TGGGAAAACTTAGAT | 93664 |
rs147504290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122714375 | TTTCAGATTGTTTCT[A/G]GCTGTCTTTAGTATT | 93664 |
rs147515855 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122637370 | GGCTAATTTCTTGTA[A/G]AGAACAGGAGGCTGA | 93664 |
rs147533640 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122392965 | ATTCCTGTCCCACAG[A/C]TTATATATGAACTAC | 93664 |
rs147534423 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122806943 | CTTAGCACCAAATCC[A/G]CTGTTTATTTTCTAA | 93664 |
rs147535319 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122448489 | TCCAAAGATGATGTG[A/C]GTATAAGAGAAATAG | 93664 |
rs147536675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122546302 | CGTGATATTATACCC[C/T]ATTAACAACGCCCCA | 93664 |
rs147553888 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122329892 | ATTTTTGTCAGAATG[C/T]GGCTTCTGATGATGA | 93664 |
rs147570514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122337585 | GGCCTCTCTGAACCA[C/T]GTCTGGACTTGCCAA | 93664 |
rs147570806 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122429998 | TAAAACACCACCCAG[A/G]TGACACACACATCCT | 93664 |
rs147577096 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122624585 | AACCTAACTAAATCG[C/T]TGAAGTGTTTAAATG | 93664 |
rs147583138 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122884344 | TCAGAACAGACTCAA[C/T]TAGAGCAGCTGATTA | 93664 |
rs147585257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122801182 | ATATAGGGAGAGATA[A/G]AGACCAAAACAGAAT | 93664 |
rs147590465 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122484713 | AGATGTGAAAAGACA[A/G]GCCATAGATTAGGAG | 93664 |
rs147600252 | in-del | -/AG | 0.0166325 | 0.0896639 | intron-variant, upstream-variant-2KB | CADPS2, LOC105375481 | GRCh38.p7 | 7:122529331 | AGGCATACAAATGAA[-/AG]AGGCATAAAAACACA | 93664 |
rs147604371 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122732929 | TATTATGTATAATAC[A/G]TATTATATACAGATT | 93664 |
rs147607062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122658546 | ACACCATGGAAATAC[C/T]ATGCAGCCGTAAAAA | 93664 |
rs147610248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122534230 | AATATGAGGGATTTT[A/G]TTTCCTAATCTTACA | 93664 |
rs147619631 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122867133 | AGAGGCTTGCCCTGA[A/C]CACCCTATCTAAAAT | 93664 |
rs147621054 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122728950 | TATAGGCACCCTACT[C/G]TGCTATCAAACATTA | 93664 |
rs147621186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122779236 | ACACCAACCAACCAC[A/G]GAATCTCAGTGCACA | 93664 |
rs147626908 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539390 | CTAAAACTGAGCTAA[A/C]TAAATTTCTGTTCAT | 93664 |
rs147657898 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122413032 | GAAAATGTCCAGGTC[C/T]GGAGCCTGGCCTGAG | 93664 |
rs147658954 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122359037 | AGGGCAAGAAATGTA[C/T]GTCTCATCATGTATG | 93664 |
rs147660521 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122510181 | TAAGTAACAAACATA[A/T]ACAAGTTTAATTCTG | 93664 |
rs147674315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122365014 | AGCTGAGCCAAAGGA[C/T]AGCAGAGATAGAGTG | 93664 |
rs147678502 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122641691 | CAGAGATTTTCTAAA[C/T]TCTTTGTAAAGGAAC | 93664 |
rs147690048 | snp | A/G | 0.000296736 | 0.012177 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698437 | AAATGGAAAATTTCC[A/G]TGCCTTTTAAGTTAC | 93664 |
rs147695041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122409417 | AAAGGTCTTCTTAAA[A/G]TTAACTTGGAAGACA | 93664 |
rs147696077 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122505966 | GTACTAACACCTGTA[C/G]CTGCTGGTTTACTAG | 93664 |
rs147696897 | in-del | -/AG | 0.0722614 | 0.17581 | intron-variant | CADPS2 | GRCh38.p7 | 7:122516923 | GGTATAGTTTACATA[-/AG]AAGTAAAATTACCTG | 93664 |
rs147708433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122753772 | ATACATATAAACACA[C/T]GAACGCTTGCATGCT | 93664 |
rs147710677 | in-del | -/TTGT | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122619194 | AGTTAATTATTACAA[-/TTGT]TTAAGATTTTTGAAC | 93664 |
rs147711450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122675953 | TGCAACAAACCTGCA[C/T]GTTCTGTACATGCAT | 93664 |
rs147715468 | snp | A/G | 0.00713621 | 0.0593058 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554729 | TTAAACGCATGATAC[A/G]GAGTGTCTATGGGTT | 93664 |
rs147718072 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122638178 | GTTCTGGGCTATAGA[A/G]CTCCCTAAGGCAGAG | 93664 |
rs147724353 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122807523 | AGGTCTGAAACCCAG[C/G]CTCGGGAGGCGGCTC | 93664 |
rs147725565 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122749525 | AATTCTGCTCAGTAC[A/C]TAAAACAGAAACATT | 93664 |
rs147732289 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122558447 | TCCGTATGCATTTCT[C/G]CTTCTTCTCATTTAT | 93664 |
rs147746847 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122679675 | GCTCAGGGGGCATCA[C/T]GGAACCTGCCGACAT | 93664 |
rs147754814 | in-del | -/TCC | 0.0138799 | 0.0821421 | intron-variant | CADPS2 | GRCh38.p7 | 7:122332702 | TCCAGATGAATTAGA[-/TCC]TCTTCAGTTACATAA | 93664 |
rs147778547 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122388448 | TTTAATCAAGATAAC[A/C]TAATACTCATTAAAT | 93664 |
rs147784737 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122582133 | CCAGAGAAAAAAATG[A/G]GATTTAACAAAATAC | 93664 |
rs147792009 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122842044 | AGTTGTTACCTCCTA[A/G]GCTGGAAAAGGAGAG | 93664 |
rs147794716 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122754677 | AAACGGGTTTCACCA[A/T]GTTGGCCAGGTTGGT | 93664 |
rs147798394 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122431484 | TCAACACCTGACATC[A/G]TGAGGAATGTGGGGA | 93664 |
rs147801982 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122533853 | GTGTATCCATATGCA[C/T]AAAAGACAGATCCAG | 93664 |
rs147813067 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122774883 | TATGTGTCTGTGTGC[A/C]TATCTATATCCACAA | 93664 |
rs147815601 | in-del | -/TT | 0.0479149 | 0.147179 | intron-variant | CADPS2 | GRCh38.p7 | 7:122519565 | GTATTAATCCCTCTC[-/TT]GGGTTATTTCAAACG | 93664 |
rs147821244 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122576610 | AGTATGCATCTGATA[C/T]GGTTAGGCTTTGTGT | 93664 |
rs147829612 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122769727 | GGGGCAATACGGGAT[C/T]GCACAAAAGGCATGG | 93664 |
rs147834125 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122383588 | ACTGTGCCTGCTTTC[C/T]CGCAGGTGATTCTGA | 93664 |
rs147850706 | snp | C/G | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122699568 | GATTCATCACATAAA[C/G]CATTATATTGCATTT | 93664 |
rs147851225 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122653212 | TGACTCTTAAGCAAG[C/T]AACATCTTTGAGATT | 93664 |
rs147869546 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122404847 | TATCTTACATATGGC[C/T]GGGCGCGGTGGCTCA | 93664 |
rs147886899 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122674943 | ACTTTTCAGGTGTTA[C/T]CAATTCATGAAGCTT | 93664 |
rs147891217 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122605019 | CTGGGCTACAAACCT[A/G]TATAGCATGTATTGT | 93664 |
rs147897064 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | CADPS2 | GRCh38.p7 | 7:122862278 | GTCCTCAAATTCACC[A/G]TCTATTCTCTGCTCT | 93664 |
rs147907913 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554327 | ATCAAGTTCCAATAT[C/G]GTGGTAGCTCGCATA | 93664 |
rs147920248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122718393 | GGGAAAAGGAGGTAG[A/G]AGAGAAGTAGAAAGA | 93664 |
rs147927517 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122600367 | GACCTTCTCTGAAAA[A/G]ACTGAGCCATGAAAC | 93664 |
rs147934189 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122844005 | GCAGAGACAGGATCA[C/T]AGACGAGTTAGTTAG | 93664 |
rs147957180 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122720667 | AGTGAGAGCCCGTGC[A/G]AAACTTTGGGATCTT | 93664 |
rs147974115 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122372660 | AAATATCTGGGATAC[A/G]AGAAATTCACTGTTA | 93664 |
rs147980875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122594180 | CAGCACACATCTGTA[A/G]TCCTAGCTATTCAGG | 93664 |
rs147983252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122842213 | CTCTTTCCTCCCTCT[A/G]CTTCTGTCAGGCTCT | 93664 |
rs147986745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122754746 | TCCCAAAGTGCTGGG[A/G]TTACTGGCATAAGCC | 93664 |
rs148010784 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122420844 | TTTTCTGTAACACTC[C/T]TTGGCTCATTGAAAC | 93664 |
rs148011994 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122521248 | TGTGAAAATGATTTT[C/T]GGTTCATTCTCAAAC | 93664 |
rs148016854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122638965 | TCTAGTCTGCCACCT[C/T]GAACCCTAAGTCCTA | 93664 |
rs148019001 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122828986 | TGGTTATCTCTTATA[C/G]CATCTTTTCTGGACC | 93664 |
rs148024187 | snp | C/G | 0.0718919 | 0.175435 | intron-variant | CADPS2 | GRCh38.p7 | 7:122644441 | TATCTGATGACACAG[C/G]CTTCATAGTTGTCTT | 93664 |
rs148033023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122880216 | CCAGTTCATTCTGGA[A/G]TGGAAAGCAACACTC | 93664 |
rs148038715 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122760550 | TAGAGAGTTCAGTAC[C/T]ATCCCTAGTTAATAC | 93664 |
rs148040989 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122682971 | AAACGATTGCTGGAA[C/T]GGCCAGTTGCTCCTC | 93664 |
rs148045339 | in-del | -/GA | 0.178465 | 0.239547 | intron-variant | CADPS2 | GRCh38.p7 | 7:122711880 | TGGTCTCGAACTCCT[-/GA]GACCTTGTGATCCAC | 93664 |
rs148062708 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122426228 | TATGTCTTTGTTTCC[A/T]TTGATACATAATCAA | 93664 |
rs148093846 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122651688 | TTTGCTTTGACACTC[A/G]GGTAAATCTGGGTGA | 93664 |
rs148102420 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122541047 | TAAAATTACTGTAAA[C/T]TGAGTATGTTAATAT | 93664 |
rs148106053 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122851391 | CCACAGAAACCATGG[C/T]CTCAGAGTGAAGGTG | 93664 |
rs148108938 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | CADPS2 | GRCh38.p7 | 7:122765032 | ACTTTCTGAAACACA[G/T]GGAGTCACACCCTGA | 93664 |
rs148115308 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122392030 | TGAGGTTGTTATAAA[G/T]ATTAAATGAGATAAA | 93664 |
rs148129652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122707418 | TATTCTTTGATCTCT[A/G]TGGGTAAGAGTGCTC | 93664 |
rs148130873 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122367429 | ATATTACAGAAATGA[C/T]CTTTTAATTCATACC | 93664 |
rs148152146 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122443166 | GATCCCCAGATTACA[G/T]TTAGCATTTCAGGGC | 93664 |
rs148154099 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122448687 | TATAGCAATCCCATG[C/T]CCATGTCAGTGACTG | 93664 |
rs148161397 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122770810 | AAGCATCAGCAGGTG[A/C]AGCAGGAGCTGCTGC | 93664 |
rs148163751 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122691181 | TGCTATCAGGTAAGT[C/T]GTCCATATGACGACT | 93664 |
rs148166304 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | CADPS2 | GRCh38.p7 | 7:122664163 | GCTGGTTTTTCAGCA[A/G]GGAAAGAATCATGTA | 93664 |
rs148177674 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122823138 | TCTATTCAGATCTTT[C/T]GTACATTTTAAATCT | 93664 |
rs148183451 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122673363 | TTGACAGGGTGCTCA[C/T]TGGTGCATTTACAAT | 93664 |
rs148185064 | in-del | -/CT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122652235 | AATGCCTAGTGAAAA[-/CT]CTCTCTCTCTCTCTA | 93664 |
rs148188008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122415361 | GCAGCATTGTAAGAC[A/G]GGTTTGTGTTCCGTC | 93664 |
rs148188816 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122453848 | AAGTCAGGGGAAGCT[C/G]GCTTGTGTCAACCTT | 93664 |
rs148191838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122552550 | ACCCCCAAATCAAGC[C/T]TTGTAAGGGGTCTGG | 93664 |
rs148197102 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122802061 | TATTTAGAAAAGCTA[C/T]AAGATGTCTAAACAG | 93664 |
rs148200244 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122718910 | CCTGCTTTCTCCTCC[A/C]ACTTGGCTTCTCTAG | 93664 |
rs148224330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122469957 | AAGATGAGTTTTGTG[A/G]TATTTGACTTTTTAA | 93664 |
rs148226374 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122565345 | GTTGAGAAATCTCTG[C/T]GATACATTTTCATAT | 93664 |
rs148228127 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122600760 | TTTACTAAAAGTTTC[A/G]TTTAATAAAGAACTA | 93664 |
rs148228502 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122868998 | ATCATTGGAAATCAT[C/G/T]GAATCTGAGGAGCTA | 93664 |
rs148235831 | in-del | -/A | 0.32153 | 0.239548 | intron-variant | CADPS2 | GRCh38.p7 | 7:122738846 | TGTCCTATTGTACCC[-/A]GGGGGGGAAAAAAAA | 93664 |
rs148239938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122325336 | ATTAATCTAACTAAA[C/T]GTGGAAGTAAACAGT | 93664 |
rs148251643 | snp | A/C | 0.21845 | 0.248001 | intron-variant | CADPS2 | GRCh38.p7 | 7:122722903 | AGTCTGATCTTTGAC[A/C]AACCTGACAAAAACA | 93664 |
rs148252315 | in-del | -/A | 0.209084 | 0.246629 | intron-variant | CADPS2 | GRCh38.p7 | 7:122337834 | ATATAGAAACAGGCT[-/A]TGACTATGACTATCT | 93664 |
rs148254402 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122646358 | ATATGTAAACATCAA[C/T]GCAAAGTACAATATG | 93664 |
rs148261283 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122534902 | ACCTCTAAATTATTC[A/G]AAAGTAGTAATGGGG | 93664 |
rs148266415 | in-del | -/AA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122814196 | AGGGAAAAAAAAAAA[-/AA]TCAAGCAGAGGTTTT | 93664 |
rs148267987 | in-del | -/A | 0.0379877 | 0.132479 | intron-variant | CADPS2 | GRCh38.p7 | 7:122375225 | TTCATCTGGAACCAC[-/A]AAAAGCTTCAAATAA | 93664 |
rs148279015 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122516047 | AGACAGAAAGCAGGG[A/G]GACAGATGGATACAT | 93664 |
rs148311248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122485686 | GCTAAGATCATTGAT[A/G]AAGTTAGCTATGCTA | 93664 |
rs148319918 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122815644 | CAAAATATATTGCAG[C/T]GAAACGTTAGACATC | 93664 |
rs148325396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122342094 | TTTCAAGATTTGATG[C/T]AAAAAAATTAAAGAT | 93664 |
rs148331962 | in-del | -/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122416569 | TAGCAAAACCCATGC[-/T]TTTTTTGTTGCTGTT | 93664 |
rs148338857 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122744066 | TGATAGGTATAGACA[C/T]GGTCAAATGACCAAG | 93664 |
rs148341774 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122668234 | AAGAGAGGGAAAATT[G/T]GAAAATTCCATTTTT | 93664 |
rs148343149 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122410330 | GCCTGGGTGACAGAG[C/T]GAGACACTGTCTTAA | 93664 |
rs148347859 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122545642 | GAACAAGTTTTGTTT[G/T]TTAGGATGGAGACTG | 93664 |
rs148359078 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122359787 | GAAACATTTGTAAAA[C/T]AAAAAGTCCAGTTCC | 93664 |
rs148361264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122396637 | CCTGTGATACAGTCA[C/T]AATGACTTTCACGAT | 93664 |
rs148373192 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122729964 | GGAAATAAAATGAAG[C/T]GTAGTCTCTACCTGA | 93664 |
rs148387300 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | CADPS2 | GRCh38.p7 | 7:122863970 | AGAAGGCAGAGGTTG[C/T]AGTGAGCTGAAATCA | 93664 |
rs148393804 | in-del | -/TATA/TATATG/TATC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122366699 | GTATATATATATATA[-/TATA/TATATG/TATC]CGTATACATATATAT | 93664 |
rs148412863 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122356165 | TCATTCAGGATACCA[C/T]GTTACATTTAGTAAT | 93664 |
rs148418627 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122492896 | TAGAGAAAAGGTCTC[C/T]GTCTGTTACCTGGGC | 93664 |
rs148421701 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | CADPS2 | GRCh38.p7 | 7:122585977 | AAAAGAGTCTAAGCA[A/G]AAACATTCATGACAG | 93664 |
rs148421720 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817200 | GCTGTGACTCGGATG[C/G]GGGGACCTCCCTTGG | 93664 |
rs148425809 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122697909 | GGAGAAACTTCATTA[A/T]TTGTCTCCTCTTCAC | 93664 |
rs148434868 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CADPS2 | GRCh38.p7 | 7:122437553 | CAGGTAAGAAACTTT[C/T]ATTTTCAGATAAGTA | 93664 |
rs148451605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122412657 | GGATTTGGTGGATGA[C/T]ATCGTATTTAAAATA | 93664 |
rs148453448 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122508734 | GAAATGATTCCATTA[A/G]GAATGAATGGATGTG | 93664 |
rs148457667 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | CADPS2 | GRCh38.p7 | 7:122634180 | TATCAGGATAATGCT[A/G]GCTTTGTAGGATGAG | 93664 |
rs148488703 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122866626 | GAATTGCTTGAACCC[A/C/G]GCAGGTAGAGGTTGC | 93664 |
rs148493488 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122746603 | CACACTAACACTAAC[A/G]ACAGCTGATGAGCTA | 93664 |
rs148496470 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122641319 | CTTGACAAATATTTA[A/G]TTCAGAAAATATGCT | 93664 |
rs148499282 | in-del | -/AGAG | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122472271 | AAAAGAAGGGAGTAT[-/AGAG]AGTTTTAAAAGGGGG | 93664 |
rs148502006 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122373952 | CAGACAAAAGATACT[G/T]CCAGAAAAGAAAACT | 93664 |
rs148507913 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122505648 | GTAATAAAATACCAA[C/T]AACTAACAGAGCTGT | 93664 |
rs148508908 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122843232 | CACACATCATAAGAG[C/T]TGCTTTTTTTTTTGG | 93664 |
rs148510070 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122598011 | TCATATATGTTTACA[A/C]AACAGATGACATTTT | 93664 |
rs148511056 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122757478 | AGCATTCTGTACTAC[A/G]ATAAATTTAGCACCC | 93664 |
rs148534998 | in-del | -/TGTATATACATACACATGTATA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122720565 | ATATATGCATGTGTC[-/TGTATATACATACACATGTATA]TGTATATACATACAT | 93664 |
rs148541013 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122831653 | CATCTCAGCACAGGC[C/G]AAAGCCTGTACTTGT | 93664 |
rs148546585 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | CADPS2 | GRCh38.p7 | 7:122716847 | GAATGGAGGGAGGCC[C/T]AGAAAGGGAAACACT | 93664 |
rs148547441 | in-del | -/AATT | 0.0217236 | 0.101931 | intron-variant | CADPS2 | GRCh38.p7 | 7:122504092 | TCATTTTCTCCCCTC[-/AATT]ACTTACTTATCCTTA | 93664 |
rs148547763 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122645318 | ATGTACATGTGTGTA[C/T]ACATGTACATATATA | 93664 |
rs148549043 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122442785 | ATCTAGTCACTCAAG[-/T]TTTTTTTTTAACAGA | 93664 |
rs148556554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122381446 | AACATGCCTTATCCC[C/T]AATGTTTTTCTCTGT | 93664 |
rs148562196 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122761450 | CCTGAGAGCTTTCAA[A/G]CATTTTTTAATCCCC | 93664 |
rs148563691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122685021 | TAAATATTTGTTGAA[C/T]AGATTTTATAGTTTA | 93664 |
rs148566425 | snp | C/T | 0.00153221 | 0.0276362 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698393 | TCCCCACCTCAACCA[C/T]GGCTGTAATGAGAAC | 93664 |
rs148578961 | in-del | -/A/AAAC/AAG/G | 0.0383715 | 0.133092 | intron-variant | CADPS2 | GRCh38.p7 | 7:122659311 | AAAAAAAAAAAAAAA[-/A/AAAC/AAG/G]CACCGTGGAAAAAAA | 93664 |
rs148592268 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122429507 | AACAATTTGTCCCTC[A/C]TCAACAGGTGACTTA | 93664 |
rs148614186 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | CADPS2 | GRCh38.p7 | 7:122728187 | AATATTTAAATGCCA[A/G]TCTTCCCAGCTCCTC | 93664 |
rs148623223 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122608221 | TCCGTCTAAAAAAAA[-/A]AAAAAAGAAGGCACA | 93664 |
rs148624768 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122402650 | AACTAATGTCTCCAT[C/T]AGTTTGAAAGGTCTT | 93664 |
rs148626976 | snp | A/C/T | 0.0158469 | 0.0875917 | intron-variant | CADPS2 | GRCh38.p7 | 7:122445673 | AGAAAATATTATCTG[A/C/T]GCATGGTGGCATGTG | 93664 |
rs148629430 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122854040 | GCCATAGTAACTGCT[A/G]GAGCGATGTCCTCGG | 93664 |
rs148629644 | snp | C/T | 0 | 0 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122542609 | ACTTTATCTATATTC[C/T]TTGCAGTATTTTCAA | 93664 |
rs148633563 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122736566 | TCTTGAAATTAGTTA[A/C]TAGCTTTAATTATTA | 93664 |
rs148635421 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122659938 | GCAAAGAAGAAACAA[C/G]GACTTTCTCAAACAA | 93664 |
rs148650605 | in-del | -/C | 0.0193772 | 0.0965046 | intron-variant | CADPS2 | GRCh38.p7 | 7:122667086 | TTTATATTAAGCGTT[-/C]CCCTGTTCAATTATT | 93664 |
rs148660525 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | CADPS2 | GRCh38.p7 | 7:122459585 | AAAAAGGGGATCTAT[C/T]TTAATATATTAATTT | 93664 |
rs148679935 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122861390 | TATATCTGTTGACCA[C/T]TTGTATATCTTCTTT | 93664 |
rs148682651 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122774547 | TAAAAGCATAGGTTA[C/T]AAATGTTCTACCAAT | 93664 |
rs148687270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122665402 | CGGCTGACAGACTTC[C/T]GTACTGAAACACTGG | 93664 |
rs148690030 | in-del | -/C | 0.0178098 | 0.0926698 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122557985 | CAGAGAACACCAATA[-/C]CCTAGGAAACGAAAG | 93664 |
rs148702141 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122787165 | GCTGAATGATTTGAG[C/T]GTAGATATCTAAACA | 93664 |
rs148703621 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122710418 | ACCAGGCCGTGTGAC[A/T]GATGTGTCATGTAGT | 93664 |
rs148708883 | in-del | -/G | 0.0494327 | 0.149241 | intron-variant | CADPS2 | GRCh38.p7 | 7:122484045 | AATTTTCCAAGGACT[-/G]ACCTATAGATTGAAG | 93664 |
rs148711545 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122321156 | TTATGTTTACATTGA[C/T]TGATTGATTGACTGA | 93664 |
rs148712708 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122417660 | TTGGGGGCCGCTCTA[C/G]CTGTTCTAATTTTGT | 93664 |
rs148717776 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554025 | CAGGAGACAGTCCCT[A/G]CATTTCTTCCCCAGG | 93664 |
rs148720203 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122636889 | TTAAATTTGTACGTC[C/T]AACTCTCTAGTGAGA | 93664 |
rs148725453 | in-del | -/AAAAAC | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122830936 | CACCACTCAGAACTT[-/AAAAAC]AAATAGAAAAACTAG | 93664 |
rs148735466 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122617974 | TGTTAACCTGGGAGG[C/T]GGAGGTTGGCAGTGA | 93664 |
rs148750000 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | CADPS2 | GRCh38.p7 | 7:122473344 | ACGTGGCTGCGCCAG[A/C]GTCTCCGAGCCTACT | 93664 |
rs148751556 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122871250 | TTCCAGCATTTTCAC[A/C]TGTTGAGTTTTCTCT | 93664 |
rs148754729 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122751994 | ATACTCCCATTAGCA[C/T]TTAGAAGCATTATCC | 93664 |
rs148770807 | snp | A/C/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122813226 | TGCAAGAAGTAAGTC[A/C/G]ATACCTACATTTTAC | 93664 |
rs148773774 | snp | A/G | 0.185472 | 0.241529 | intron-variant | CADPS2 | GRCh38.p7 | 7:122724036 | CCTGTTGTGGGGTGG[A/G]GGGAGGGGGGAGGGA | 93664 |
rs148787842 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122537920 | AAATAATATTAATAG[A/C]TAAATCTAATAATAA | 93664 |
rs148789727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122623726 | TGTTTGCTTATTAAT[C/T]ATGCGTTGAATAAAA | 93664 |
rs148801270 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122386856 | ATCAAAAAGGAGAAA[C/T]TGACATGAGCAAAGG | 93664 |
rs148804346 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122484165 | TAAAAGTGAATAAAC[G/T]TATTTTAAAAATTCA | 93664 |
rs148810009 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122679732 | TTAAAATTTCTCTCT[C/T]TTGTACTCTTTCCCT | 93664 |
rs148819175 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | CADPS2 | GRCh38.p7 | 7:122324076 | GTAAAATAAATAACA[A/C]CATATAAGAAGTGTT | 93664 |
rs148827035 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122689830 | CAGTGCTGCTCTATA[C/T]ATGGTGGTGTCCGCA | 93664 |
rs148829588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122638491 | GTTTTCTGTCAAGAG[A/G]GAGTAGAGCAATCTG | 93664 |
rs148845114 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122619554 | ATCACTTGAACCCAG[G/T]AAGTGGAGGTTGTGG | 93664 |
rs148854077 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122344466 | ATAAATGAAACATGA[C/T]GATCACAGTATACAA | 93664 |
rs148858852 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | CADPS2 | GRCh38.p7 | 7:122477624 | TCAAAGCTAGGAGGA[C/G]AGAAACAGATGTAAT | 93664 |
rs148861014 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122677207 | GCTTGATAAATACTA[A/C/G]TGAGAATTTCTGGTG | 93664 |
rs148874625 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122814977 | GAATTATTCCTAGGT[C/T]GGCCCCAGAACTCTT | 93664 |
rs148877343 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122725628 | GTCAGAATGGCTTAT[A/T]ACTAAAAAGTCAAAA | 93664 |
rs148896399 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539735 | TATAACTCTGCCTGT[C/G]TGTCCCTCTCTCTCT | 93664 |
rs148898005 | in-del | -/CC | 0.021333 | 0.101051 | intron-variant | CADPS2 | GRCh38.p7 | 7:122328560 | GTCTACACAGGAATA[-/CC]AAGCAGTAAGTGTAT | 93664 |
rs148898353 | snp | A/G | 0.0839998 | 0.186933 | intron-variant | CADPS2 | GRCh38.p7 | 7:122625120 | CAATGGCACAATCTC[A/G]GCTCACCACAACCTC | 93664 |
rs148909028 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | CADPS2 | GRCh38.p7 | 7:122353471 | CTTCTTCCTTCCTCA[C/T]TGTTTTGGTCTTTTC | 93664 |
rs148911083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122391033 | GTATCTTCAAAACCA[C/T]GGTTGCTTTTATATT | 93664 |
rs148912495 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122485437 | TTTGAATGGTCTGGA[C/T]AGATCAAACCAGCCA | 93664 |
rs148946384 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122779622 | CCATAATATAGAACT[G/T]AGTATAGACTTCTTG | 93664 |
rs148948394 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122495505 | TTCTGATGCTTAACC[A/G]TCTTGATATAAATAT | 93664 |
rs148948750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122700369 | GGGCCAACAAAAACT[A/G]GTATAAAAAGAATAC | 93664 |
rs148978409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122414413 | ACTGCAATTGAATAT[C/T]CAATTATTAATAGAT | 93664 |
rs148979442 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122883802 | TGCTCAATGCTCTAA[A/G]CATTTAGAATGTGGA | 93664 |
rs148981672 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122512052 | ATTAAAGTTGACCAA[C/T]TATTAGTTCTAATCA | 93664 |
rs148999860 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122707157 | ATACTTAACCATTAA[C/T]CGCAACAAACATGTA | 93664 |
rs149014731 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | CADPS2 | GRCh38.p7 | 7:122835828 | TGAAAGTGACGGGGA[A/G]AATGGAACCAAGTTG | 93664 |
rs149016557 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122748712 | CAGCAGAAGGCAAGG[A/G]ACTTTCAGCTCATCA | 93664 |
rs149030130 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122844337 | TTAAAAAAACATCCC[A/G]CTTGCCCTTGACTCC | 93664 |
rs149030324 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122375976 | TGGCCAACAGGTATA[C/T]GAAAAGGAGCTTAAC | 93664 |
rs149032506 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122468717 | GCAAATTTCAGAGCC[A/G]GGATTCAAGTGAAGA | 93664 |
rs149037521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122600576 | AATGAGTTTGCCACA[A/G]CAGAAATCAAGACCC | 93664 |
rs149037522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122652710 | TTTGTTCTATGAATG[C/T]GCACCACTGCAGATA | 93664 |
rs149067574 | in-del | -/TTTTTTAGAT | 0.311123 | 0.242413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122816250 | CACGAGATCAATTTA[-/TTTTTTAGAT]TTTTTTAGCTCCCAA | 93664 |
rs149069042 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122718740 | GCTGTGGTCAAGCTG[A/C]AGCGCTGACCACTGA | 93664 |
rs149071465 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122643229 | AACACGGCCTCAAAA[C/T]AATGGTCAAAAGTTT | 93664 |
rs149076826 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122480309 | ATAATTTTTTTTTTA[A/T]TTTTCCTAGTTATTG | 93664 |
rs149084260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122764350 | GTCCTATTTATAACT[A/G]TATCCTCAGCAACCA | 93664 |
rs149085189 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | CADPS2 | GRCh38.p7 | 7:122383044 | CTTGTATGTTCATTG[C/T]CATGCTATTCACAGT | 93664 |
rs149089234 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122658579 | GATGAGTTAATGTCC[C/T]TTGTAGGGACATGGA | 93664 |
rs149100193 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122358682 | AGAGACAGCTTCAGA[C/G]AGGCATACTTGCTGG | 93664 |
rs149105725 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122582954 | ATGTTCATTTTTAAT[A/T]CCCAAACCTCCTGCA | 93664 |
rs149122206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122534626 | TTTGTAAATTATTGA[A/G]TAAATATAGGCCAGG | 93664 |
rs149124427 | snp | A/C | 1.64985e-05 | 0.0028721 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122697955 | CAGGCAGTTCATTTG[A/C]CATTAGAACTTGCAA | 93664 |
rs149152208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122857175 | ATGGCATCATTAACC[A/G]AGGAAAATAGGCATG | 93664 |
rs149153356 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122409723 | GTCTTGTCTACAACC[C/T]GTCCCCTTCTCTTTC | 93664 |
rs149156960 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122739574 | TCACAAAATAAGCCA[C/G]AGTCACCTGGCTAAA | 93664 |
rs149169852 | in-del | -/ATATATAT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122579451 | ATAAAATTGCATCGA[-/ATATATAT]ATATATATATATATA | 93664 |
rs149179103 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122707101 | GCAGGCACAATGGCA[-/G]GTTACAGGCTCTAAA | 93664 |
rs149189997 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122461899 | TCGCCTGGCCTGCCA[A/G]GAGCCTTCTTAATGG | 93664 |
rs149190898 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122839966 | AATCATACCTCTATA[A/C]AGAGACATGCACACA | 93664 |
rs149193063 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122558649 | ATCAAATTTAATATA[C/G]AGGAGGAAAAACTAA | 93664 |
rs149206522 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122863377 | GATGTGATGTAGGAT[A/G]AAGAACAATTATTCA | 93664 |
rs149207979 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CADPS2 | GRCh38.p7 | 7:122776100 | TATATGGTTTGGCTG[C/T]GTCCCCACCCAAATC | 93664 |
rs149212470 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122667863 | AGAATAACACTGCAA[A/G]GCCATTTGAGGGAAA | 93664 |
rs149227520 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122791210 | AGACATCACAGTCTT[A/G]TATAATAAATTATTC | 93664 |
rs149230088 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122609818 | AGAAGGATGAATTTA[C/T]CTCCAACAAAGCACA | 93664 |
rs149247942 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122555318 | GTGATTATTTCACAA[A/C]CCTCACTTCACAGAA | 93664 |
rs149260881 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122742122 | CAAACTGGGCGCAGC[A/G]GCTCATGCCTGTAAT | 93664 |
rs149263934 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122411824 | TCTTGAGGGACAGAC[A/G]AATGAACAGGTGACA | 93664 |
rs149270011 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122633430 | TGGTTAGATGTATTC[C/T]TGGGTTTTTTGTTTG | 93664 |
rs149274923 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122873805 | GTATAAAAGCATTCC[C/T]GTTTCTCCACATCCT | 93664 |
rs149285149 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122612545 | GGAAATTGAAGGTCT[A/G]AATACATAGAAAGAC | 93664 |
rs149299988 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | CADPS2 | GRCh38.p7 | 7:122465314 | AGCCTGAGAATTTCT[G/T]TAGCTACAACATAAA | 93664 |
rs149301478 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122560902 | TTTATTTAGCAGATG[C/T]TAATAACCACATATA | 93664 |
rs149311044 | in-del | -/TTTTC | 0.00914312 | 0.0669923 | intron-variant | CADPS2 | GRCh38.p7 | 7:122824537 | GCCATTTGTATTTAG[-/TTTTC]TTTTAACTGTCTGTT | 93664 |
rs149312837 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122746013 | AGCAGGTCCCTTAAC[C/T]TCAGTGCCTCAAGTT | 93664 |
rs149315437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122669725 | TCCACATCACACATA[C/T]TCTGAAGGCCATCAC | 93664 |
rs149321531 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122526544 | GAACTCCTCTGTACA[A/C]ATACTCTCTGGGTTC | 93664 |
rs149324926 | in-del | -/TAAT | 0.0524604 | 0.153226 | intron-variant | CADPS2 | GRCh38.p7 | 7:122447334 | GTAGTACAATCTAAT[-/TAAT]ACAACTCCAAGCTCT | 93664 |
rs149328477 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122879940 | TTTGGACATAGCAGA[A/C]CTTAAACAAGTCATT | 93664 |
rs149329230 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122795382 | ATAAATTCCTGGACA[C/T]ATACACCCTCCCAAG | 93664 |
rs149337396 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122573732 | TAATTCATTCACAAA[G/T]AAAAGTGCACTGGCA | 93664 |
rs149346974 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122810638 | TTTATTCGCAGGATT[G/T]TATCTATATTGTTAG | 93664 |
rs149351044 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122422398 | TTGTGGACTGCTTGC[G/T]GGCAAAACTTATCTA | 93664 |
rs149353974 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122522627 | ATTATTAACTATAGT[C/T]ACCCTATTGTGCTAT | 93664 |
rs149354792 | in-del | -/T | 0.0256215 | 0.110247 | intron-variant | CADPS2 | GRCh38.p7 | 7:122595215 | ATTACCTTTTAAAGA[-/T]TAAAAAGTACTAGAG | 93664 |
rs149383812 | snp | C/G | 0.030278 | 0.119257 | intron-variant | CADPS2 | GRCh38.p7 | 7:122756823 | GAGAATTGCTTGAAC[C/G]TGGGAGGCAGAGGTT | 93664 |
rs149384835 | snp | A/G | 0.00232057 | 0.0339838 | intron-variant | CADPS2 | GRCh38.p7 | 7:122345722 | ACAAAATAATATCAG[A/G]TCTCAATTGTGAAAT | 93664 |
rs149385551 | snp | A/C | 0.000202204 | 0.0100529 | intron-variant | CADPS2 | GRCh38.p7 | 7:122441584 | ACAGTATCTTTAAAA[A/C]CAAAAGAAAGAACAA | 93664 |
rs149391497 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122580369 | CTGAGGCACAAGAAT[C/T]GCTCGAATCTAGGAG | 93664 |
rs149403570 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122697077 | GCCATGACTAAGTAT[C/T]AAAGTCGTTCTATGT | 93664 |
rs149416909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122860671 | TACTATGCAATAGAA[C/T]ATCAGGATTTCTCTT | 93664 |
rs149420856 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122405594 | CTTGAACTTCGGAGG[C/T]CACTGGAAGTGCCAC | 93664 |
rs149424840 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | CADPS2 | GRCh38.p7 | 7:122501767 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 93664 |
rs149428816 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122627261 | CAAGGTTTGTAGGAT[A/T]ATTGTCAGAAAATAA | 93664 |
rs149437898 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122355731 | AGAGAACTGGACAAG[A/T]ACTCACATGGTGACA | 93664 |
rs149443023 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | CADPS2 | GRCh38.p7 | 7:122488391 | GCTGCAAGAGAAACG[C/G]CTGAGTGAGCACCCC | 93664 |
rs149473082 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122782136 | TGAGAATAAAGAAAA[A/G]CTATTGATATTGTGT | 93664 |
rs149475218 | snp | C/T | 0.00250196 | 0.0352806 | intron-variant, synonymous-codon | CADPS2, RNF148 | GRCh38.p7 | 7:122701947 | AATGCGTACTACATC[C/T]TGGGGTTTGTATGTG | 93664 |
rs149475468 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | CADPS2 | GRCh38.p7 | 7:122368959 | TAAGAAAATGGGACT[A/G]GAATCCAACTTTTCT | 93664 |
rs149479497 | in-del | -/TAG | 0.0626037 | 0.165477 | intron-variant | CADPS2 | GRCh38.p7 | 7:122484969 | CTTTTTCATTATTAG[-/TAG]ATCTATCACGGTCAT | 93664 |
rs149481270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122589821 | AGTAGGGACTTCTAC[C/T]TTACAAGTATGGGCT | 93664 |
rs149490025 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122833061 | GGAAAAAAGATAGAT[G/T]CACTATCCATGCACA | 93664 |
rs149498398 | in-del | -/AGAA | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122527917 | GAGACAGACAAACAG[-/AGAA]AGAGAGAGAACCTAA | 93664 |
rs149503698 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122885025 | GACTACAATCTCTCT[C/G]GATCTCTAGGTCTTG | 93664 |
rs149527409 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122373652 | TACCAATGTAAGGCT[A/C]CAGGGATCATGAAGA | 93664 |
rs149527666 | in-del | -/T | 0.0154538 | 0.0865337 | intron-variant | CADPS2 | GRCh38.p7 | 7:122736891 | AAAATGAGAAACCCA[-/T]AAAAATAATAAAACT | 93664 |
rs149540086 | snp | A/C | 0.0314385 | 0.121371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122837720 | TACACTCTCCCAACA[A/C]TAAACCAGGAAGAAG | 93664 |
rs149543835 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122750745 | CCCCTGAAGAGCTTT[A/T]TTTAAAAAATGCAGG | 93664 |
rs149547700 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CADPS2 | GRCh38.p7 | 7:122646096 | AGCAGATTTGAACTC[A/G]AGTTTCAACATAATA | 93664 |
rs149551007 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | CADPS2 | GRCh38.p7 | 7:122617815 | TTGGGAGGCCAAGGC[A/G]GGCATATCATGAGCT | 93664 |
rs149556680 | snp | C/G | 0.0364509 | 0.129988 | intron-variant | CADPS2 | GRCh38.p7 | 7:122846698 | AAGAGTGAATAGGCT[C/G]AGCACACAAAAATGA | 93664 |
rs149562495 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122729850 | AGAGGTACTAATACA[C/T]GAGGGGTGGTAACTG | 93664 |
rs149563591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122378867 | CTTCATCTCTACTTA[C/T]ACAGTGAAAGATCAT | 93664 |
rs149564455 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122655154 | AAGTGAAATCTAATC[C/T]TAGTGAAGATGCTGT | 93664 |
rs149565690 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122472281 | AGTATAGAGAGTTTT[A/G]AAAGGGGGCAGGGTA | 93664 |
rs149592693 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122804526 | TTTTTAATAGAAAAT[G/T]TCTTAAATGACATTT | 93664 |
rs149595604 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122396484 | AAATATGAAACTAAG[A/C]ATGTCACTCCTAAAG | 93664 |
rs149595855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122719636 | AATAACTTCTGTCCA[C/T]GCTACACCATCAAAT | 93664 |
rs149601265 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122530885 | CAAGACCATTCCTTG[C/T]ATTCTGGGGAGAGGG | 93664 |
rs149602118 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122537874 | ATAAAAAATAATTTT[A/G]AAAAAGGATAAAAAC | 93664 |
rs149609657 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122853706 | TCTTGAAGATATGCA[C/T]ACATTGTTCTGTATG | 93664 |
rs149611025 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122767229 | CAGGATCCTTCCTGG[A/G]TTTTAGACACTAAAC | 93664 |
rs149615509 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122659836 | ATCATGCAAACAAAA[A/C]GACAGTGTGGTGAAA | 93664 |
rs149618458 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122369124 | GCTAGAAGAATTTTT[-/G]TTTCCCCCCCCCCCC | 93664 |
rs149632717 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122453293 | TTACAAAGCAGTGCA[C/T]CATGAGCTAATACTA | 93664 |
rs149637487 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | CADPS2 | GRCh38.p7 | 7:122585082 | GAAGGCTTAAATAAC[A/G]TGTTCTCAGGCAAAG | 93664 |
rs149650497 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122435004 | CTCAGGTTTTTTGCT[A/T]TAAATTTGTATCAAA | 93664 |
rs149655821 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122533714 | GACCTAAGTAGAAGA[A/G]CTAATTACATGGAGT | 93664 |
rs149657715 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122619323 | ACAAATTATTTTTTT[A/C]ATCAATAAATTTAAA | 93664 |
rs149659976 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122850124 | ATCCATCAACAACTC[C/T]GAGTTTTAGCAACTG | 93664 |
rs149663950 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122732345 | GAAAACTTTTTTTTT[C/T]TGAGATGGAGTAATT | 93664 |
rs149672007 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122477006 | GGGAGGGGAGAGGAG[A/G]GGAGAGGAGAGGAGA | 93664 |
rs149676414 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122865546 | AGAAGTATCAGCAGT[A/C]TCTGGCTTGTATCTG | 93664 |
rs149694610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122807726 | GATACCCTCTTGCTA[C/T]ATCCTCACATGGCCT | 93664 |
rs149694989 | in-del | -/G | 0.030665 | 0.119967 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122550635 | GTAACCTTTGAATTA[-/G]GAAAATAATTTTATT | 93664 |
rs149697703 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122721665 | ATCAACAGAAAAAGA[C/G]GGAATCCTCCCTAAC | 93664 |
rs149701521 | in-del | -/AAGAT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122424782 | TTATGAAGTAAGAAA[-/AAGAT]AGCTCTCACAGGGAC | 93664 |
rs149704350 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122397861 | CATACTCAAGTATGA[C/G]AGAGTGAAAAGGGCT | 93664 |
rs149705544 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122492481 | ACAAAATACTGTAAA[G/T]GGGGAATGTTTCATT | 93664 |
rs149709120 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539543 | AGAGGGGCTGGTGAT[A/G]GTGAGTCATTAAAAG | 93664 |
rs149710081 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122856517 | CAAACTCCTCTTCCT[C/G]CCACTAATCTTCCTG | 93664 |
rs149732174 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122784744 | GGAGCCATCTGTATA[C/T]ATCATTAGAGAATTT | 93664 |
rs149737015 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122320894 | ACATCTAAATGTCTG[C/G]ATGAATTTTGCCCTT | 93664 |
rs149739783 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122455173 | TAGTCCTCAAACACA[A/G]GAAGCAAGCTCCAGG | 93664 |
rs149742864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122553816 | ATAGTAAGAAAAATG[A/G]CCCCTTTTCTTTCCT | 93664 |
rs149744978 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | CADPS2 | GRCh38.p7 | 7:122587476 | CTGTATGGTATTCCA[C/T]GGTGTATATATACCA | 93664 |
rs149771559 | in-del | -/T | 0.0498117 | 0.149749 | intron-variant | CADPS2 | GRCh38.p7 | 7:122514373 | TTTAGGGGCTTAAGA[-/T]TTTTAGACTTTCACA | 93664 |
rs149784446 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122748401 | ATTTCATGGCACAGA[C/T]CCATATGCTGAAGCC | 93664 |
rs149785239 | snp | A/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122743224 | AACTAAATTTTATAA[A/T]TCTGACCTGGCTGTG | 93664 |
rs149792187 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122413325 | GGAAAGGAACTTAAA[C/T]TATCTTTCTAAGGAG | 93664 |
rs149798964 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122875251 | TGATAAACTCCACCA[A/G]AAGAAAGTAAAATCA | 93664 |
rs149815322 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122614666 | GAACCTGAAACATCA[A/T]ACTGTTGGCAAAAAG | 93664 |
rs149823104 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122727781 | ACAATAGGAATCTCA[C/G]ACATGAAAACACATT | 93664 |
rs149823701 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122335098 | AGTTTTAATCTCAAC[A/G]TTTCCCACCATTTTT | 93664 |
rs149829843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122467607 | GCAAGCACATCTGAG[C/T]TGGCGTTTGTCAGGC | 93664 |
rs149832113 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | CADPS2, LOC105375481 | GRCh38.p7 | 7:122563864 | ATTAAAAACCAACTA[C/T]AGGTTGTGCATTCCT | 93664 |
rs149840257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122671919 | AATGAACCAGTAAGG[C/T]TTACTGATTCCTATT | 93664 |
rs149851951 | snp | C/T | 0.000230768 | 0.0107392 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698269 | CTCCGGTTCTGAATC[C/T]TTGCTAAACAAAGTC | 93664 |
rs149853241 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | CADPS2 | GRCh38.p7 | 7:122882423 | AAACTCAAATAATGA[A/G]AAGAGCAGTGACTAG | 93664 |
rs149859579 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122684707 | AATGTTAACAAGGAA[G/T]TTGGGAGGAAAGAGA | 93664 |
rs149868392 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122576072 | TCCAGGGCAGCATAT[A/T]GCATTTCGTTGTCAT | 93664 |
rs149873321 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122772881 | TAAGCTCTTGACAGA[A/G]AAGGACTTTCCAGGC | 93664 |
rs149883271 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122424599 | AGAGATGATAGTGAT[A/G]GAATTACAGAGAATA | 93664 |
rs149884311 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122526118 | TTGACGTGTTAGTTG[G/T]TCAGAGACATTTCTG | 93664 |
rs149891428 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122824163 | ATAATACAGTAAACT[C/G]AGTGTTTGCTTATAT | 93664 |
rs149900358 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122497844 | AATGGTTTAGTTACT[C/T]ACATAGTGTTTTAGC | 93664 |
rs149908578 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | CADPS2 | GRCh38.p7 | 7:122759343 | TCAGCCAGCAAAAGG[C/G]AGAGTTAAAGACACA | 93664 |
rs149912701 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122652109 | CCTCTTCATGATGTA[A/T]CCAGAACCAGAGATT | 93664 |
rs149913138 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122351665 | CCATTACTGCAGAGT[C/T]CTTGTCCTGGATCAG | 93664 |
rs149916933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122445298 | TCAATTTAGAGAGAA[C/T]TGACAACAATATTGA | 93664 |
rs149921842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122582500 | ACAGCTTAATTTCTA[C/T]TTTAGACTTCCAGAA | 93664 |
rs149928421 | snp | A/G | 0.0441095 | 0.141807 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122700140 | GTACACTTTCTTGGC[A/G]GTGAATCTCAGTGGG | 93664 |
rs149941639 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122830612 | ATTTGTAACAAATGC[A/G]AAAACATTGGATTTC | 93664 |
rs149952155 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122408672 | CCTCAAGTGATCTGC[C/T]GGCCTTGGCCTCTCA | 93664 |
rs149953925 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122504856 | AGGTATCATCACCAT[A/G]CCCAGTCCGTTTTCA | 93664 |
rs149957884 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122629006 | TTTAAGAGAAGTCTA[C/T]AAAAGTTATCATTAA | 93664 |
rs149967991 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122358474 | TTAAGTTCAATTTAT[C/T]AATTTTTTTTCTTTC | 93664 |
rs149990504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122603102 | CAAAACCAATGTTGA[C/T]AGAGAATATATGACA | 93664 |
rs149998523 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122705025 | TCCCAAAACTCTCCC[A/G]ACCCCGATGGGTGGT | 93664 |
rs150000251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122674427 | CAGTAAATTTTAACT[C/T]ACATACAGCCTTCAA | 93664 |
rs150002018 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122370054 | GTTTCTGCAGTTTCT[C/T]TTACTTAAATGGTCC | 93664 |
rs150005022 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | CADPS2 | GRCh38.p7 | 7:122461279 | GAGCTTCAGATGAGA[A/G]GAAAAAGATTGTAGA | 93664 |
rs150011555 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122834991 | AGACTGCCTCCTCAA[C/G]TGGGTCCCTGACGCC | 93664 |
rs150035878 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122385614 | CCTTTACGCATAAAG[A/G]TTTTCTAACCTTGTA | 93664 |
rs150040796 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122518089 | TATTATGCTCCACTA[C/G]GCAATAGATTTTGTT | 93664 |
rs150043732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122609679 | GTACCAACCTCACAC[A/G]CTGTTTCCTCCTAAT | 93664 |
rs150049985 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122712553 | ACCCAGGGATTCAAA[C/G]ATGAGGTCATGGTTA | 93664 |
rs150052078 | in-del | -/TC | 0.030665 | 0.119967 | intron-variant | CADPS2 | GRCh38.p7 | 7:122696511 | TCCATGACCCCATGG[-/TC]CATGGAAGCAGTTAT | 93664 |
rs150057062 | snp | A/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122538156 | TTCAGTAAAAAAAAA[A/T]AGAGAAACAAAGTGA | 93664 |
rs150066348 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122753760 | AAGCTCAGTTGTATA[C/T]ATATAAACACACGAA | 93664 |
rs150067591 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | CADPS2 | GRCh38.p7 | 7:122723910 | GGAAACCATCATTCT[C/G]AGCAAACTGTCACAA | 93664 |
rs150070222 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122647484 | ATAGAAGTCTTTCTG[A/C]CAGTTTGTAACAAAA | 93664 |
rs150089612 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122381949 | TAGATATGACTTACA[A/C]TAATATTACAACTGC | 93664 |
rs150094320 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122761828 | GGCGAAACCACATCT[C/T]TACTGAAAAAAAAAA | 93664 |
rs150097469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122606488 | GACCATGGAACTAGG[A/G]CCTAAATTGAACACA | 93664 |
rs150097833 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122794294 | CTCGGAGGTTTTGTT[A/C]ATTTCCTTCTCATTT | 93664 |
rs150099173 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122714691 | ACTCATAGGAATAAG[A/T]CTATTTACTCACAAG | 93664 |
rs150102592 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122676809 | CATGGGACAAGATTC[A/C]GAACTCACTGTAAGT | 93664 |
rs150109567 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CADPS2 | GRCh38.p7 | 7:122372774 | AGTTAATATAGAAAC[C/T]GCATATTTTAATTTT | 93664 |
rs150111819 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | CADPS2 | GRCh38.p7 | 7:122464545 | AAATAAAAATGACAT[A/C]TTTACAGTAGAGAAA | 93664 |
rs150125624 | in-del | -/ACACAC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122762030 | TATATATATATATAT[-/ACACAC]ACACACACACACACA | 93664 |
rs150128519 | snp | C/T | 0.000249374 | 0.0111636 | intron-variant | CADPS2 | GRCh38.p7 | 7:122438296 | TTCAGTTACTAGGCA[C/T]TGTTGGCTCTCACTG | 93664 |
rs150134157 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122769538 | GCACAGAGCTTAAAA[C/T]GGAGAATTCCTCCTC | 93664 |
rs150144850 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122390491 | TATTTGGAATGTATA[C/T]ATTCTTTAACAACAC | 93664 |
rs150148351 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122521706 | ACTAAAGAAAAACCA[A/G]TAACTCCTATTGTTG | 93664 |
rs150150930 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122611559 | AAGACAATGAATAGA[A/T]CTATAACATGAGATC | 93664 |
rs150165372 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | CADPS2 | GRCh38.p7 | 7:122842517 | ACTTTGATGCTTAAT[A/G]TCAAAAACCAAAAAT | 93664 |
rs150170316 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122725337 | GTGAAAACATCTCTT[A/T]TATATATATATGTAT | 93664 |
rs150170822 | snp | A/G/T | 3.29654e-05 | 0.00405978 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698636 | TCTCTGAGTACTTTG[A/G/T]TCGGCTGAAAATGGT | 93664 |
rs150172966 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122649593 | TTCTATTCATTCTAA[C/T]GTGCATACAAAGTTG | 93664 |
rs150181774 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122494912 | TTTTGGTAATCACTT[A/C]AAGGTTTCAGTTTCC | 93664 |
rs150182261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122851651 | GCCACACAATCATGG[C/T]GGAAGAGGAAGAAAG | 93664 |
rs150186715 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122622173 | TTACCACAGATATGC[A/G]TTGTTGGAAGAGTAT | 93664 |
rs150197608 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122345514 | ATACCATCAAAATTC[A/G]ACTTTTCTCTTTGCA | 93664 |
rs150202474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122867723 | AATAAACTTATCTGA[A/G]CCTAAATGGGAAACA | 93664 |
rs150203156 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122573373 | TTGTGAGACTCCATC[G/T]CTATACAAAACAAAA | 93664 |
rs150217817 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122551079 | TAGTCGTGGACTGAT[A/T]AGTTATCAGAAACAT | 93664 |
rs150220448 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122634570 | TCCTTCTTTGTTAAT[A/C]TAGCTAGCAGTCTAT | 93664 |
rs150223054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122690629 | ACTGGTTGGAGAAGG[C/T]CATCCTTCCTCTCAT | 93664 |
rs150239275 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | CADPS2 | GRCh38.p7 | 7:122741661 | ACATATTAATCTGTA[C/G]AAAATCTACAAAAGT | 93664 |
rs150241184 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122664280 | TGCCCAACAGCTGGG[A/G]GGCTAGAATATACCT | 93664 |
rs150251777 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | CADPS2 | GRCh38.p7 | 7:122873572 | ATCCAGTCTATGATT[C/G]ATGGGCATTTTTGGT | 93664 |
rs150255604 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122786100 | TCTTCTAACTATAAC[G/T]TCTAGTAGTCTCGTC | 93664 |
rs150262989 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122323059 | GGGAAATGATCATTA[A/T]AAGCAAAACCATGTA | 93664 |
rs150267840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122457500 | ATGACCCTCAGGGAT[A/G]CCCAAATATTTTGTA | 93664 |
rs150270932 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554945 | ATAACGAATTAATAG[C/T]ACAACAAGCCACAGT | 93664 |
rs150307112 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | CADPS2 | GRCh38.p7 | 7:122750589 | TGTCTGAAAAAGCAG[C/T]TCAAAGGAAATTTCC | 93664 |
rs150312699 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122642783 | AAAGGGGGATTAATA[A/G]CTGTTTTTCCATAAT | 93664 |
rs150323480 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122514943 | AATAATTCCAAAATA[C/T]TACTAATAGTATCTT | 93664 |
rs150323511 | snp | G/T | 0.0349115 | 0.127424 | intron-variant | CADPS2 | GRCh38.p7 | 7:122878283 | AAAAAAAAAAAGTGG[G/T]AAGGGAAAGACGAAT | 93664 |
rs150338084 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122439668 | AAACTTTATCATTCT[C/T]TCTCTATCAAATTCA | 93664 |
rs150341970 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817748 | CCTTCACTCTTAGCG[A/G]CAAGTCCTGCTTTTC | 93664 |
rs150351969 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122339248 | ATACAAAGAAGTGTA[C/T]TGTGAAAGTTCTATT | 93664 |
rs150359170 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122566305 | AAGGGAACCCTTGCA[C/T]ATTGTTGGTAGGAAT | 93664 |
rs150373738 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122884734 | TAGTGTTAACTATAG[G/T]TGTGTACTTATCCCC | 93664 |
rs150381087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122685835 | TCTTACAATCAAGGA[A/G]GAAGACAGTAATTCA | 93664 |
rs150390817 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122446913 | GAATCACTTTCATTG[C/T]TTTATGTTTAATGTC | 93664 |
rs150394884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122578262 | AGTAGCTCTACCATC[C/T]AGAGACGAACACCAA | 93664 |
rs150395498 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122775279 | TCTGCCATAGCGTCA[C/T]AGACGCTGACACAAT | 93664 |
rs150397935 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122696317 | CTGCTAAATCCTCCA[C/G]TAGTCCAGTGCTATG | 93664 |
rs150410767 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122734387 | AAAAAAAAAAAAAAA[A/G]AAAAAAAAAAAAGAA | 93664 |
rs150411579 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122826937 | AATAAACATAAGAAC[A/G]TAAATCAATGAAATT | 93664 |
rs150415636 | in-del | -/T | 0.291493 | 0.246533 | intron-variant | CADPS2 | GRCh38.p7 | 7:122626181 | TTTTAGGAACTTTTC[-/T]TTTTTTTCTCAGCAA | 93664 |
rs150428377 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122845796 | ACAAGCAACAGGAAA[A/T]CTTGATAAATTGTCC | 93664 |
rs150429581 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122591240 | TCCCACTCACAATTG[C/T]TTCAAAGCGAATAAA | 93664 |
rs150450224 | snp | A/C/T | 4.97701e-05 | 0.00498828 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122701909 | TCAATGCATGCCTTA[A/C/T]GGAAAAAATGTTTGC | 93664 |
rs150465939 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122832866 | ATACTGAGAATGAGA[C/G]ACTGCTGGCTTTTTT | 93664 |
rs150467717 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122744630 | ACAGTGTTGACAGGA[C/T]GATTTAAAAGCCCAA | 93664 |
rs150477708 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122375647 | TAACTTAAGACCTCA[A/G]ACCATAAAACTTCTA | 93664 |
rs150482038 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122506502 | CCATTTTGTCCTCAA[C/T]TGCCAACCTGTGCAA | 93664 |
rs150486136 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122631063 | AATATGCAGTAAGTA[C/T]GGGTTCCAGGTTAAC | 93664 |
rs150495463 | snp | A/T | 0.0126879 | 0.0786318 | intron-variant | CADPS2 | GRCh38.p7 | 7:122360741 | GAACTGCAATTTTTT[A/T]TTAAAGAATTCCATA | 93664 |
rs150500040 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122449109 | CAAATTTATTTATTG[A/T]TTAAAACAGTTGGAG | 93664 |
rs150500202 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122778160 | GAGGTGGTCTCAGAT[A/G]GAGATAAGGAACCTG | 93664 |
rs150502188 | snp | C/T | 1.64906e-05 | 0.00287142 | intron-variant, synonymous-codon | CADPS2, RNF133 | GRCh38.p7 | 7:122698205 | TTTTACTACTCGAAG[C/T]TGGAGTTGTCCAAAT | 93664 |
rs150502790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122546564 | ATCTTAAGCTTTTTC[C/T]TTCCTTTTTTCAGGG | 93664 |
rs150504387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122581128 | CTTAATCATGAATCC[A/G]AAGAAGTTAAAACTG | 93664 |
rs150517445 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122829766 | ATAAAACCTCTATGT[C/T]ATAATATTTATTTTT | 93664 |
rs150517682 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122397205 | GACAGCAAATGATTA[C/T]ATCCTGCAGAATTTA | 93664 |
rs150520039 | snp | A/G | 0.000148379 | 0.00861205 | intron-variant, stop-gained | CADPS2, RNF133 | GRCh38.p7 | 7:122698246 | GATCTGTTGTTAATC[A/G]CTGCCATCTCCGGTT | 93664 |
rs150530195 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122477083 | GAGAGAGAGAGAGAG[A/G]GAGAGAGAGAGGTAG | 93664 |
rs150538683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122595394 | TAAGTGGGGGTTATG[C/T]TCTTTGGGGCCAGTC | 93664 |
rs150553617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122454919 | AGTACGCAGGCAGCC[C/T]CTTGGTCTTTCTCCT | 93664 |
rs150554227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122703502 | CAGTGTAAACTCTTA[C/T]TGTTAGCCTAATACA | 93664 |
rs150563342 | in-del | -/GC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122325009 | ACATATAAGAGGCAT[-/GC]GCTTCCAAAAGGATT | 93664 |
rs150567944 | snp | A/C | 0.030278 | 0.119257 | intron-variant | CADPS2 | GRCh38.p7 | 7:122834874 | GCAGGGCATAGCTGA[A/C]CAAAGGCAGCAGAAA | 93664 |
rs150572879 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | CADPS2 | GRCh38.p7 | 7:122719449 | GAGCTGCCACCTTAG[C/T]GCACTGGCATGTGCA | 93664 |
rs150575524 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122644599 | ACCTGTATTTGAAAG[A/G]TTCTTGGACTCCAAT | 93664 |
rs150590491 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | CADPS2 | GRCh38.p7 | 7:122509403 | GCAGAAACTTCAAGT[C/G]ATGATTCTGACACAT | 93664 |
rs150592592 | snp | A/C/G | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122602319 | CAATCTTCATCTTAC[A/C/G]ACCATTGCAATTTTA | 93664 |
rs150616172 | in-del | -/GAG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122812423 | TGGAAAAAAAAAAAA[-/GAG]AGAGAGAGAGAGAGC | 93664 |
rs150622967 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122482021 | TCTCCAGAGGCAGAC[A/T]CTGTCTAAAAAAATT | 93664 |
rs150627217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122608857 | CACTTATATTTTATT[A/G]TGGTACTGCACTGGA | 93664 |
rs150630757 | in-del | -/TT | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122402268 | AGTTCAAGGACTCTC[-/TT]GTCTTCCTTAAAAAG | 93664 |
rs150636247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122334317 | CCTCTCTAGCATATG[C/T]TCAGGTCTATTGGTA | 93664 |
rs150640523 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122810268 | GGTAAGTAAGGAGGT[A/T]AATAAGGAAGCTTGT | 93664 |
rs150657084 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | CADPS2 | GRCh38.p7 | 7:122859726 | ATAGTATTTACATAC[A/G]GTATTCTCCTGTATA | 93664 |
rs150658746 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | CADPS2 | GRCh38.p7 | 7:122771271 | TTTATAATGCTTTGT[A/G]AAAGGATTAGACTAA | 93664 |
rs150659781 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122541222 | TTTTTTTTTTGAGAC[A/G]GAGTCTCACTGTTGC | 93664 |
rs150661614 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122626820 | AAAGTGTTAAGTAAC[A/G]TGCCTACTATTATGT | 93664 |
rs150672638 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122392785 | ATATTCTTGAAACCA[C/T]TCTTCCAAAGGTTTT | 93664 |
rs150675704 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122487325 | AAACATAACTTTTAT[A/G]CACACTGGGAAACCA | 93664 |
rs150678081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122524261 | TCAAATGTTATTTAA[C/T]ATTACATGTAATACA | 93664 |
rs150679967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122614517 | TTTTCTAAAGGTAAT[A/G]CACAAATGAAGGCCA | 93664 |
rs150688660 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122843434 | CTATGGGGTGTCACT[C/G]TCTGTCAAAAAGCTA | 93664 |
rs150696257 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122651739 | GAATGAGATTATAAA[A/G]GATTAATGAAAGCTG | 93664 |
rs150707303 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122368594 | TTCTTAATCAGACTG[A/G]CATCAATGCTTTGAT | 93664 |
rs150707425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122824115 | AAAATTATCACCCAA[C/T]ATTTAAAAGAAATAA | 93664 |
rs150707482 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122403258 | GGTAAAAGTCACTGC[A/G]TTTTATTTCAGTTCC | 93664 |
rs150710135 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122737160 | CTGTATATTAGATTT[C/T]ACATCTAGAATTAAC | 93664 |
rs150713550 | in-del | -/GAA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122678874 | CTGAAACCATGGCAG[-/GAA]AACATAAATTGTGAA | 93664 |
rs150724057 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122350446 | ATTTGAATAAAAATC[G/T]CCTGAAATTTTTCAA | 93664 |
rs150724066 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122869509 | AAAATGTAGGGGAGA[C/T]AAAACTTTCTCAGAC | 93664 |
rs150731470 | snp | G/T | 0.0356815 | 0.128715 | intron-variant | CADPS2 | GRCh38.p7 | 7:122674099 | TACTTCCCGGGGCCA[G/T]CGGTGCTGGCTGGCC | 93664 |
rs150731953 | in-del | -/AC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122719013 | CTATGCCATAAATGT[-/AC]ACAATTTTGAGGAAG | 93664 |
rs150746419 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122692025 | CATATGGCCTTTGGT[C/T]GTCTGGTGCCACCCA | 93664 |
rs150746485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122553182 | GTCTTACAGCACTTA[C/T]CACTATCATAATTAT | 93664 |
rs150749103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122636131 | ATGTGAGATTTTGAT[C/T]CTGTTATTTCGTTAG | 93664 |
rs150762734 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122408107 | AAACATTTGGTATTA[C/T]ACTTTATAAGATTTT | 93664 |
rs150763303 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122869567 | CTAGACCTGCTTTAC[-/A]AAAAAAAAAATGCTA | 93664 |
rs150777694 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122875115 | TCCAGAAATGTGAGT[A/G]TGTATACGTTTGCAG | 93664 |
rs150778275 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | CADPS2 | GRCh38.p7 | 7:122788137 | CCAGCTTCAGGGTTA[A/G]TAGGAAACAATACTT | 93664 |
rs150783468 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122678701 | AAAGGCCGATCTTAG[A/G]TTCTACATAGTGATG | 93664 |
rs150794074 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122325804 | TTTAAATGAATTAAC[A/G]TTACAGTCTTTCAGC | 93664 |
rs150798920 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | CADPS2 | GRCh38.p7 | 7:122460209 | GCATAAGCCACAACA[A/G]TTATATATTAAATGT | 93664 |
rs150800193 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122557402 | TCACAGTGCCTGCCA[C/G]ATAGGATTTCATTAT | 93664 |
rs150810922 | snp | C/T | | | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122697916 | CTTCATTATTTGTCT[C/T]CTCTTCACTAGGTGA | 93664 |
rs150825653 | in-del | -/GGCACAATCTC | 0.0670745 | 0.170406 | intron-variant | CADPS2 | GRCh38.p7 | 7:122686743 | AGGCTGGTGTGCAGT[-/GGCACAATCTC]GGCTCACTGCAACCT | 93664 |
rs150832146 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122427651 | AGGCTCTCATTTATA[C/G]ATGGATCTGACCCTA | 93664 |
rs150846857 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122880359 | ATATCACCTAGACAC[C/G]TTTTATAAGTCTAAA | 93664 |
rs150851460 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | CADPS2 | GRCh38.p7 | 7:122760815 | TGGGGCCTGTTGTGG[A/G]GTGGGGGGAGGGGGG | 93664 |
rs150853588 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122517224 | GCTGTACGTAGTTAA[C/T]ATCAGAAGCCCACTC | 93664 |
rs150884107 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122342336 | GGCCAATGTCATGTT[A/T]TTGGTCTTAAGCAAT | 93664 |
rs150889744 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122569435 | TAGGAAGAATCAATA[C/T]CGTGAAAATGGCCAT | 93664 |
rs150901370 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122888598 | GTTTTCTCCATGAAG[A/T]TGAAGATGACTTAAG | 93664 |
rs150906876 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122687922 | AATTTTTTACATTTA[C/T]CTCATTTAATTAGTC | 93664 |
rs150940804 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122648804 | TGCAAAAACAGTCTC[A/G]TAGATGAAGTCCAGC | 93664 |
rs150942322 | snp | C/G | 0.021333 | 0.101051 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122532972 | AGAATGCCCAACCTA[C/G]TGCTTTGCCCATAAC | 93664 |
rs150946018 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122572305 | AATCACAGAAAAGTT[A/G]TCCTTCCTCCTTAAA | 93664 |
rs150952771 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122849781 | CTGTCCCCAAGCCAG[C/T]CCCCAGCCCTCTCCC | 93664 |
rs150955406 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | CADPS2 | GRCh38.p7 | 7:122761855 | AAAAAAAAATTAGCC[A/G]GGTGTGGTGGCATGC | 93664 |
rs150958672 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122389883 | GCACATGTATCCCAG[A/C]ACTTAAAGTAAAATT | 93664 |
rs150979455 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122586649 | TTTCATCTTATTTCT[A/G]TTCAACAAAAAGGGA | 93664 |
rs150988163 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122408187 | TACTGTTATTTTTTT[-/T]TTTTTTACCAATTAC | 93664 |
rs150992298 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122443591 | TTTTTAAATACAGTA[A/T]TTTTTTTTTTTACCA | 93664 |
rs150994640 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122437875 | CAGTACATTGCAAGC[A/T]ATTAAAAACCGAAGG | 93664 |
rs151006842 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122768087 | ACAAAGTAAAATGTG[G/T]TGATGAAAGCCAAAC | 93664 |
rs151010074 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122690009 | CAGTGTGCAGTTCTG[A/C]ACAGAAGCTGGATGC | 93664 |
rs151024603 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122780527 | CCTGTCCCATCAATA[A/T]TCCGATTTAGCCCAT | 93664 |
rs151028675 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122671758 | AGGCAATGGAAAACA[C/T]GAAAGAAGGAAGTGA | 93664 |
rs151029285 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122452312 | ATCTCATATTCACTT[C/T]AAAACCTGTTTATAT | 93664 |
rs151031509 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122550555 | TCTCTTTTTCAGTTA[C/T]AGATTTAATTGTCAT | 93664 |
rs151045282 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122400309 | GGGTGTGGTGGTGCA[G/T]GCCTGTAATCCCAGC | 93664 |
rs151045502 | snp | C/G/T | 0.00637247 | 0.0561273 | intron-variant | CADPS2 | GRCh38.p7 | 7:122717645 | TTATACAACCTGCAG[C/G/T]AACCGAAATCTTTCC | 93664 |
rs151061374 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122733824 | ACTGGGAACCTAGTG[C/T]AAAATCTTTCACTAT | 93664 |
rs151062435 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122375113 | ATAGTCAAAATGTCC[A/C]TACTACTTAAAGTGA | 93664 |
rs151068343 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122598827 | ATACTGAGGATACGA[C/T]GTTGAATAAGACCTG | 93664 |
rs151076314 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122867565 | GCTCTTAAATCACCA[C/T]GCCTGAGGAATGGCA | 93664 |
rs151076952 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122785816 | TCTCACTAGGGCTCA[A/G]ACCATTTAGAGGAAG | 93664 |
rs151077207 | in-del | -/C | 0.0410537 | 0.137264 | intron-variant | CADPS2 | GRCh38.p7 | 7:122790500 | AAATGTTTCTAATCA[-/C]CACCTACCCCTGGCC | 93664 |
rs151083402 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122456949 | ACGCAAAAACTCTTT[C/T]ATATACATTGAACAT | 93664 |
rs151100373 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | CADPS2 | GRCh38.p7 | 7:122645353 | CATGTACATGTGTGT[A/G]TATACATGTACATGT | 93664 |
rs151119926 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122512609 | AGTTGACTTAAAAAC[A/G]TATTTATGTGAACAG | 93664 |
rs151143684 | in-del | -/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122543068 | GAATAAAGTAAGTTA[-/T]TTTTTTTTAATAATC | 93664 |
rs151151865 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122685564 | ATTCATTCTTTTCAG[A/G]TCTTTGTTCAGCTCA | 93664 |
rs151153315 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122484327 | GATAGATAAACTGAC[A/C]AAAGAAAGGATAGCC | 93664 |
rs151155694 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122575286 | CTGGGGGAGAATACC[A/G]GCTTTTATTGACATG | 93664 |
rs151166620 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122813530 | AAAACTACTGTCACT[C/T]GTAAATTACCTCACT | 93664 |
rs151169136 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122338893 | AGCCTCCGAAGTAGC[C/T]AGGACTACAGGAACA | 93664 |
rs151171430 | in-del | -/TCA | 0.0715223 | 0.175059 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122562693 | CTTTTAAATTTCTCC[-/TCA]TAAGTGTGTGATTTA | 93664 |
rs151189877 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, nc-transcript-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122543042 | GTTAATATACATTAA[C/T]ACTCAAGGAAGAATA | 93664 |
rs151192524 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122628847 | AATGTTAGTCAGAAC[C/T]ACTATGTGCCAATAA | 93664 |
rs151205513 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122394506 | GTGGCCCTCAAAGTG[A/C]AAATGTGCTGATTTA | 93664 |
rs151206576 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122489725 | TGAAATCCTATCAAA[A/G]CAAATTTGATTTTGC | 93664 |
rs151217155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122844402 | ATTCTTTGTTCACTA[C/T]TACAACTCTCATTTC | 93664 |
rs151218412 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817703 | TCTCTGCTTTTCTGC[A/G]GGAGGGGCAAGTACC | 93664 |
rs151221016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122728364 | AGTAAATATGAAGAG[C/T]TGAGGTATAATGTTA | 93664 |
rs151233598 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | CADPS2 | GRCh38.p7 | 7:122861927 | AGTTCTGAGGGAGAA[C/T]GATTTCAACCTGGAA | 93664 |
rs151236798 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | CADPS2 | GRCh38.p7 | 7:122740267 | TTATGTCCACACAAA[C/T]ACCTGTACACAAATG | 93664 |
rs151237410 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | CADPS2 | GRCh38.p7 | 7:122369420 | ACAGGCGTGAGCCAC[C/T]GCGCCCAGTCTTCCC | 93664 |
rs151242879 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122500286 | CGTATAAAATGGCTT[A/C]CACAGTGTGTGGCAC | 93664 |
rs151244540 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | CADPS2 | GRCh38.p7 | 7:122590505 | GGCTGCGCTATAATT[C/T]AGTCAATCACTCTTC | 93664 |
rs151248984 | snp | A/G | 0.000148377 | 0.00861198 | intron-variant, synonymous-codon | CADPS2, RNF133 | GRCh38.p7 | 7:122698469 | AATCATAACCACAAC[A/G]ACATCTTCAAATGCC | 93664 |
rs151250283 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122871627 | GTCAATGTCTGAAAA[C/T]GTGGCTTGTGTGAAA | 93664 |
rs151257190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122353750 | GCAGAAATCTTCAGT[A/G]CCACACCTGGCAAAC | 93664 |
rs151259454 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122446684 | CCAGGGAATCATTTG[C/T]AAATAGCTGTAGCTC | 93664 |
rs151273422 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122696149 | CAGTGGCCAAAGAAT[A/G]ACAATTTATCCTGAT | 93664 |
rs151286444 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122826241 | CATGCCAACTAGGGC[G/T]GAGTGAGGAACCTGC | 93664 |
rs151293157 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122642324 | ACCTAATGTAACAGT[C/G]TATTAGTCTTGCCTT | 93664 |
rs151296043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122506416 | AATCAGGTTTCAGCA[C/T]CACTGCTTTTGATAG | 93664 |
rs151301947 | in-del | -/AAAAC | 0.208474 | 0.246527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122331641 | GAGACTCTGTCTCAA[-/AAAAC]AAAACAAAACAAAAA | 93664 |
rs151303233 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | CADPS2 | GRCh38.p7 | 7:122877813 | AGGAGCATGTACTTT[A/G]TAGGCATCTCATTTC | 93664 |
rs151307381 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122758830 | GCTGCAAACCATTAA[C/T]GTTTTTAAACTAATC | 93664 |
rs151327353 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CADPS2 | GRCh38.p7 | 7:122423873 | TAGGGAATGCACTTC[A/G]AGAACTACCAGTAGT | 93664 |
rs151331354 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122559387 | ACTTAGCCTCAGTCC[A/G]TTTCCACCGCTCTCC | 93664 |
rs180670871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122667810 | AAAGGATACTTCAAG[A/G]AAAAGAAAATAAAAG | 93664 |
rs180675628 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122628778 | ACTTCATCTGCCAGA[C/T]TGCATACTAGATACT | 93664 |
rs180684525 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122651849 | AAAGGAAAATTATAG[C/G]AGTAGATATGGTACT | 93664 |
rs180693778 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122636854 | CTTGTATACTATCTT[A/G]CCAGAATTCTCTGTA | 93664 |
rs180695204 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122595439 | AAATGTTTTGCTTTA[C/T]ATTTTCTTAATTTGA | 93664 |
rs180696974 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122695719 | ATCAAACAAGCACAC[A/T]GTGTTAAATGTTAAA | 93664 |
rs180698534 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122707150 | AGGAATAATACTTAA[C/T]CATTAACCGCAACAA | 93664 |
rs180700692 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122610425 | ATTCTGTAGAAACTA[C/T]GATAAGCAAAAAAAA | 93664 |
rs180703980 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122675355 | AAAGAACAATGGTCA[C/T]GTACCGGAAAAGGCC | 93664 |
rs180711043 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122645438 | GTGTGTATATATGTA[C/T]ATATACACACACATA | 93664 |
rs180711462 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122681299 | AAGAAAGAGCTCTCC[A/G]GTCCGTGCCTCCAAG | 93664 |
rs180717290 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539152 | TCATGTGTCAGACAC[G/T]TAAAACCTAATGCAA | 93664 |
rs180719067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122556448 | CACTTACAGACTTTA[C/T]TGTTTTTTAATTCTT | 93664 |
rs180719719 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122659910 | CTATATCCAGTGAAA[G/T]TATACTTTAAATGCA | 93664 |
rs180723055 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122575857 | TTTAGAATAATTTAA[G/T]ACTTACAGAAAAGTT | 93664 |
rs180729398 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122586835 | CTGACTGTTGCACAT[A/C]TGTAAGAAAGTTATG | 93664 |
rs180735936 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122601113 | ACATCTACCATACTT[A/G]AAAGTGAAGTAATAA | 93664 |
rs180746146 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122619470 | AATACAAAAAAAAAA[A/T]AAAAAATTTAGCCAG | 93664 |
rs180750383 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122519032 | AGAACACAAATATCA[A/T]CAGTTTTCATGGCCA | 93664 |
rs180754902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122546919 | GAGCCTATCTAAATG[C/T]GAAAAAAAAGTGTAC | 93664 |
rs180757211 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CADPS2, LOC105375481 | GRCh38.p7 | 7:122529398 | ACTGAAAAAAGTATA[A/C/T]CCATCCCTAATTTTA | 93664 |
rs180763537 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122565747 | TTTACACTATACAAC[A/G]TGTTTTAATATCCAT | 93664 |
rs180773993 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122401770 | AGAGCGAAGTGAGAG[C/T]TTGGTCTTTTTTGGC | 93664 |
rs180779165 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122784687 | AGGTTGGTTCTCACA[C/T]TTCATCCTTTTCTTA | 93664 |
rs180779314 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122374466 | AAGAAAAGAAATACA[A/C]GGCATGCAAATCAGG | 93664 |
rs180780878 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122354398 | GGATTCAACCGCCAG[C/G]AGTTCGGTTCCTCAG | 93664 |
rs180786811 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122382309 | AAATGTAATTAATGA[C/T]TATCTGTAAAAGTAA | 93664 |
rs180787027 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122332767 | AAATTGGGAGCTGCA[A/C]AAGCTCTTTCCAGTT | 93664 |
rs180788125 | snp | A/G | 0.0810805 | 0.184299 | intron-variant | CADPS2 | GRCh38.p7 | 7:122822584 | AAGCCAAGCCATCGC[A/G]TCCCCTGTGACTTGC | 93664 |
rs180789936 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122806313 | AAAAGTGTTTAGAAC[A/T]GGTAATAATCATAAT | 93664 |
rs180796356 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122838012 | TATGCCTGATGAATA[C/T]TGATGCAAAAATCCT | 93664 |
rs180805046 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122342820 | AATACTCTAATTGGA[A/G]TAGCAAAAGTTCGTC | 93664 |
rs180805696 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122858447 | TAAGGATTTAGAGGC[A/C]CAAAAGCCTCAGTTC | 93664 |
rs180808910 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122722522 | GGAGAACTACAAACC[A/G]CTGCTCAACGAAATA | 93664 |
rs180824274 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122363095 | AGCACTTTCTTCCTG[A/C]CTGTTAGGATTTCTT | 93664 |
rs180824617 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122718185 | CTAAGCTAGAAGCTT[G/T]ATATATGTAGTTTAT | 93664 |
rs180833973 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122689769 | TAGTGATCGTGTTAT[A/G]TTTGCACAAACCTCA | 93664 |
rs180835087 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122746228 | GTGAATAATTAACAA[G/T]AGATGGATCCACAGT | 93664 |
rs180835727 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122835008 | GGGTCCCTGACGCCC[A/G]AGTAGCCTAATGGGG | 93664 |
rs180842590 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122560696 | AGTAGAGCCTATCTC[C/T]ACAAGAAACCTTGAC | 93664 |
rs180849511 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122703186 | TTTCTTCCTTAGTTC[G/T]GGAGAGACTGAAAAT | 93664 |
rs180849952 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122542363 | AACACACCTAACACT[C/G]TCGTTCTCTCAGATA | 93664 |
rs180861488 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122580129 | TGGAAAATATCTCTG[A/C]ATACAGTCTTCAGGT | 93664 |
rs180871867 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122764169 | CTGACTCAGCTTAGA[C/T]ATCACATTCTCCAGA | 93664 |
rs180888611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122729070 | TCGTTTGCTACCTCC[A/G]TGTGATCAACTCTCT | 93664 |
rs180892564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122484066 | TAGATTGAAGGCATT[C/T]CCAGTAAAATCTCCA | 93664 |
rs180895824 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122523280 | ATATAGATGTCAATG[C/T]ACTGTCACCTAGAAA | 93664 |
rs180921912 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122850062 | GATGAAGACCTGGGG[A/G]CCTTGCTTGGCAACA | 93664 |
rs180922676 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122879632 | ACAAGCAATCAGAAA[G/T]AAGCAAATTAAATAT | 93664 |
rs180927121 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122503840 | GCCATCTCATAGAGT[A/G/T]AGAATGGAGGAGATA | 93664 |
rs180927659 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122476081 | CAGAATATTAAAACT[G/T]CAAATCACACATTTT | 93664 |
rs180933740 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122449944 | TGCTACTAGCCCCAG[C/T]TGAAAAATCACTAAT | 93664 |
rs180941407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122413083 | AGCTGTGCATCTGTG[A/G]TGAGTTGCTCAACTT | 93664 |
rs180944626 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122459497 | CTGCAGTGCATGAAA[G/T]TATTAATTTTCCTGC | 93664 |
rs180951876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122423552 | GTGACATCGCTAAGA[C/T]GTGGCACTGCCAACT | 93664 |
rs180958201 | snp | A/G | 0.00202359 | 0.0317443 | intron-variant | CADPS2 | GRCh38.p7 | 7:122438495 | GTGGAAGGGTGAGGG[A/G]CAGGGTTGGGGATAG | 93664 |
rs180959398 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122392862 | AAGAATCCTCAAAAT[G/T]CTTTGTATACATAAG | 93664 |
rs180961152 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122685722 | TCCCACTAGCAAGTA[A/T]GCTCCATGATGGCAG | 93664 |
rs180968702 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122672130 | TTCTTACAGAAATAA[C/T]AATAGAGTTTAAGAC | 93664 |
rs180972475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122432501 | AAAAAATTAGCCAGG[C/T]GTGGTGGCAGATGCC | 93664 |
rs180973669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122705276 | ACAGAGAGAGAGACT[A/G]GATGATTGAGGCTAC | 93664 |
rs180974702 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122871433 | AGCACAACAAATACA[G/T]GCATATGTACATTTA | 93664 |
rs180976759 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122470040 | TTGTGGAGACAAGAA[G/T]GGGCAGATGGAAGAG | 93664 |
rs180980065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122632608 | TAGATCTTTGTCAGA[C/T]GCATAGTTTGCAAAT | 93664 |
rs180987343 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122534371 | CTCCCAACATAGTCT[C/G]TAAGTGATATTTCAG | 93664 |
rs180989622 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122713355 | CCTATCTAAACTCAT[A/G]TGCCTTAGTTCCCTT | 93664 |
rs180990388 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122657150 | TTCTGAGGACTCTGC[G/T]CTGTTCCATAGGTCT | 93664 |
rs180994619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122726112 | TCAGAGGCAAAAGAA[C/T]GCTTTTCCCAATGAT | 93664 |
rs180996213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122700075 | AAAGCTAAAGGATGG[C/T]ATGTGGACTCACAAG | 93664 |
rs181005181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122720495 | ATGTATATATGTATA[C/T]GTATATACGTATAAG | 93664 |
rs181009788 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122692446 | CATGTGACTCTGCCA[C/G]CGAAGGTATGCTTTT | 93664 |
rs181013587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122597675 | AAAGTCCATTTGTAC[A/G]TATTTTAAAATCAAA | 93664 |
rs181017994 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122614482 | ATTTAGAATAAAGAT[G/T]AAATAGAAGAAAAAA | 93664 |
rs181022840 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122751625 | AAAAGGGTCTCACAA[C/T]ACACACGGCACATAC | 93664 |
rs181023413 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122732797 | TATAATATATATACA[G/T]TATATATTATATACA | 93664 |
rs181023930 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122648151 | AAATGGCTTCTCTTG[C/G]ATTCCCTGATGCCTC | 93664 |
rs181034905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122625137 | CTCACCACAACCTCC[A/G]CCTCCCAGTTTCAAG | 93664 |
rs181040364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122607188 | CACTACAGGTTTCTG[A/G]GTGATTTAGAAGGAA | 93664 |
rs181051712 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122677151 | CTTCCTAGAGCTTAC[A/G]GTGGGGCAAACAAAT | 93664 |
rs181064710 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122776506 | GATACCCAAAAATGT[A/G]GAAGTGACTTTGAAA | 93664 |
rs181067409 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122640882 | GAGTTTGCAGTGAGC[C/T]GAGATCACGCCACTG | 93664 |
rs181070130 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122663728 | TACATGGTAACTAAT[A/G]TCATAATGTTGGCCC | 93664 |
rs181077670 | snp | C/T | 0.117188 | 0.211804 | intron-variant | CADPS2 | GRCh38.p7 | 7:122592125 | GAATCTACAAAGAAC[C/T]CAAACAAATTTACAA | 93664 |
rs181078109 | snp | A/G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | CADPS2 | GRCh38.p7 | 7:122318031 | CTCCGATTTTCTCAT[A/G/T]AGGATGCAAGTAGCT | 93664 |
rs181079399 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122754702 | GTTGGTCTCAAACTC[C/T]TGACTCAGGGGATCT | 93664 |
rs181079852 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122797338 | TTGACTCAGCAATCC[C/T]ATTACCAGGTATATA | 93664 |
rs181082734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122439006 | AATACCACGGCAGTG[C/T]ATTCAAAGAGGGAGA | 93664 |
rs181083746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122870311 | CAGGGGTAGCTATAC[A/G]TATCAGGCAAAATAG | 93664 |
rs181084854 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122353054 | TGTGCTCATCGAATT[C/G]TGAATTCTCATAATG | 93664 |
rs181090261 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122332084 | TTCCAAAAAAGCCCA[C/T]TCAATTTTTTTTGCA | 93664 |
rs181090820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122838394 | TGCCCTCTCTCACCA[C/T]TCCTATTCAACATAG | 93664 |
rs181093780 | snp | A/C/T | 0.0107286 | 0.0724924 | intron-variant | CADPS2 | GRCh38.p7 | 7:122815876 | AGGTTAATTTAAAAA[A/C/T]AAATTAAAAGTTTTA | 93664 |
rs181097623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122834671 | AGGGTCCCACACCCA[C/T]GGAGCCTTGCTCACT | 93664 |
rs181099242 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122848712 | TATTTCCATGTTAAT[A/G]GACTGTATTAGTATC | 93664 |
rs181101481 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122460711 | ATGAAATAATTATAA[A/G]AGATCTAAGGAAACA | 93664 |
rs181101753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122823389 | TATACAGTGTTTAAC[A/G]TAAGTGAATCTCTCT | 93664 |
rs181104806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122423848 | CCAGGTGATGCTCAT[A/G]ATGCTGGTGTAGGGA | 93664 |
rs181108788 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122880385 | CTAAATAAATATGCA[C/T]TAGCCTCTCCACTGT | 93664 |
rs181110706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122858892 | TGAGAAAAAAAATAA[A/G]TTGCCAGTAAAATGT | 93664 |
rs181115581 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122382996 | ACTAAACCAAACAAA[C/T]GAAAACAAAAACAAA | 93664 |
rs181124025 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122402516 | CTATTTTTAAACATC[A/G]AAGCATACAAATTTT | 93664 |
rs181136983 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122344046 | AGTAAAGGGTAGAAA[A/C]ATAAAGCATGAAAGA | 93664 |
rs181138351 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122363850 | TGCCTTAGAATTACT[C/T]AGTGACAAAGAGGAA | 93664 |
rs181141640 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122747207 | AGAAAGCCATTCCCC[A/C/G]CAACACCCAGCCACC | 93664 |
rs181164485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122729861 | TACACGAGGGGTGGT[A/G]ACTGGAATGAAGAGG | 93664 |
rs181166249 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122785045 | ATATTTATGCTCTGG[A/G]ATTTGAGATGTGTTT | 93664 |
rs181176543 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122764794 | AAGGAAATGTACTGC[A/G]TGCATCGAAGGCAGA | 93664 |
rs181179747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122807835 | GAAGGATACCAGTAA[A/G]ACCAGATTAGGGATC | 93664 |
rs181193622 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122623855 | TGAAAGTTCTGATAT[A/G]CTAACGCTTTGCTTT | 93664 |
rs181197744 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122571047 | ATAATAATAAAAAAA[A/T]TTAAAAAAGAGAATA | 93664 |
rs181200504 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122590182 | AAACAAACAAACAAA[A/C]AAACAAAGTGGAATG | 93664 |
rs181204757 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122616183 | TCAAAATTTAATTTA[C/T]AAAATAGATTAAAAT | 93664 |
rs181205342 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122347039 | ATCCATCGACCTAAT[C/G]ATAGGTAGGTAGAAC | 93664 |
rs181206958 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122598123 | ATTGTTTTGTGAGTC[C/T]TTATTTCCATAGGCA | 93664 |
rs181207552 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122606416 | TGTCTTGCTTATCCA[G/T]GTAGCCTCATAGTTT | 93664 |
rs181210927 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122543151 | AATAGATTCTGTGAA[A/C]CCCTTATTTATGGTA | 93664 |
rs181212181 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122323001 | TGGTTATGGGCCTTC[A/G]CAATTCTCTACATGT | 93664 |
rs181213295 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122720620 | TACGTATACATACAT[A/G]TATGTACGTATGTGT | 93664 |
rs181216509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122532260 | CTTATATGGACACAG[C/T]TGCACAATCACGGGC | 93664 |
rs181217942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122484521 | ATGGTTGTAAAATGT[A/G]AACGCCAAAATTGTA | 93664 |
rs181221985 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122733442 | ACATACATTCTAGAA[G/T]TTATAAGGTCTGCAT | 93664 |
rs181224479 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122640595 | CATTACAATTTAAAA[C/T]GTTTCCATGCTGTTC | 93664 |
rs181230091 | snp | G/T | 4.98484e-05 | 0.00499216 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122581181 | GACCACAACTCACCC[G/T]TCCCAGTTCTTTATC | 93664 |
rs181232533 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122656563 | GAAACACTTATGAAG[G/T]TTACAGGTCCACTAA | 93664 |
rs181241152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122561488 | GATGGGAGGATTAAG[A/G]ATAAAGCAAGGAAAA | 93664 |
rs181243347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122551998 | TGTTTGCCAATACAT[A/G]TTTACACACAGGTGT | 93664 |
rs181246844 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122664539 | AAGAGACACCAGAGA[C/T]TTGGCCTTAAATCTC | 93664 |
rs181249824 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122648769 | TCCAAAGGACAATAC[A/T]GAGTGCAGACCCAAG | 93664 |
rs181253391 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122504097 | TTCTCCCCTCAATTA[C/T]TTACTTATCCTTATT | 93664 |
rs181257582 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122633091 | CGATGCTGTTTTGGT[G/T]ACTTTAGCCTTATAG | 93664 |
rs181258122 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122476979 | ATGGGGTGGCGGGAA[A/G]GGGGGCGGGAGGGGA | 93664 |
rs181270801 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122692587 | ACTGGGTACCACAGC[C/T]CATGCTGCGGCCACA | 93664 |
rs181272718 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122677657 | AAACAACAACAACAA[C/T]AACAATAAAAACCCA | 93664 |
rs181274240 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122470909 | AAAGTGTGGATTAGG[A/G]AAGTGGCTAAGAAGA | 93664 |
rs181274520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122513941 | ATAGTAACGAAGATG[C/T]CATTGGGTAGTTTTA | 93664 |
rs181276896 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122494199 | GGCAGCACCAGCTTC[C/T]GCAGGAGTTCCAGCC | 93664 |
rs181286067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122752256 | TATTAAGAAACCCTG[C/T]TTACTCTATAAAGAT | 93664 |
rs181289546 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122523602 | GTATATATTTATGGT[A/G]TGCAACATGTTTTGA | 93664 |
rs181320403 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122790835 | TAAAATCCAAGCTGC[C/T]GTACAGCCAAGCTCT | 93664 |
rs181341913 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122671173 | GTAAAAAATTTAATT[A/C]TTATCTCTTTTCCTC | 93664 |
rs181359858 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122488752 | AAGAATCTTGAATTA[A/C]TTGAATTATAATCTG | 93664 |
rs181380109 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122454391 | GAACCTAGGTCTCTT[A/G]CCCTCCAAAGACGAT | 93664 |
rs181384808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122474262 | TATTAAATGAGTCAG[A/G]AATAAAATGCTGGTT | 93664 |
rs181389967 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122435982 | GAAGAGAACATGAAG[C/T]GGTATTATTCACAGG | 93664 |
rs181395019 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122398369 | TAATCCAATTTTATA[A/G]TGCTCATCCTCTTCC | 93664 |
rs181399978 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122769792 | CCAATTGTTGACTGT[A/G]TAACCTTGGACATGT | 93664 |
rs181403611 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122418619 | ACAGTGAACTATGGA[A/C]AGATGATAGTAGGAA | 93664 |
rs181403714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122781873 | TTTCAAAAATAACCA[C/T]GGTGAAATATGAAAT | 93664 |
rs181407944 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122819024 | AACCCCACAACAGGA[C/T]TTAATTAACCTCGCC | 93664 |
rs181408456 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122810630 | TATAACCATTTATTC[A/G]CAGGATTTTATCTAT | 93664 |
rs181416194 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122803458 | TTGGAGTCTGAAAGA[A/T]CGCTACATTGCTGCC | 93664 |
rs181417914 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122379149 | AAAATGACAACAATT[A/G]TAGGAAAAGCCAAAA | 93664 |
rs181425672 | snp | A/C | 0.0260105 | 0.111035 | intron-variant, utr-variant-5-prime | CADPS2 | GRCh38.p7 | 7:122885738 | CCGCGGCGCGGCCGG[A/C]GCTGTCGGTCTCTGT | 93664 |
rs181425791 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122836798 | CCTTAGAGATCTACA[A/G]AGAGACTTAGACTCT | 93664 |
rs181431634 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122854759 | GTGATAGTCTTCCAA[A/C]AGTGTTTGGTATAAA | 93664 |
rs181431827 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122875699 | TGATTAAATATGTAA[A/C]TACTGGTTCAAGGAA | 93664 |
rs181432370 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122828105 | TTTGATACATATCCA[C/T]TTAGGATCATCATGT | 93664 |
rs181438098 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122656905 | ATGTCCTGAATGGTA[A/T]TGCCTAGGTTTTCTT | 93664 |
rs181438318 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122863000 | CAACACTATTCTCTT[C/T]TTTTGACATTTTGAA | 93664 |
rs181440385 | snp | G/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122560139 | AGAATAAGACTTCAT[G/T]TAAGGTTTAAGTTGG | 93664 |
rs181442567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122640803 | GCCGGACTTGGCGGC[A/G]GGCGCCTGTAGTCCC | 93664 |
rs181444145 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122386930 | GCTAGAGAACTTGGT[A/C]TTTTCAATCCAATCA | 93664 |
rs181450856 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122359339 | ATGGTCATCCTGTAA[C/G]CACTGAAATAATTAA | 93664 |
rs181454603 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122770376 | ATTATTATTATTATT[A/T]ATTTTTTATTTTTGG | 93664 |
rs181455751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122684229 | GATATCATTATATGT[C/T]GTTTCACTTAAAAAT | 93664 |
rs181462771 | snp | C/T | 0.000127951 | 0.00799744 | missense | CADPS2 | GRCh38.p7 | 7:122387117 | ACGGAAGCTGGAATG[C/T]GCAAGTCAGTTGTTT | 93664 |
rs181463682 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122624458 | TGGGGTTCATATCAC[A/G]GGATTGTTTCTCTAA | 93664 |
rs181464544 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122752557 | TGAAGAAAATGTCAA[C/T]ACATAGGGCAAATTT | 93664 |
rs181464670 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122836417 | ATGACAGGATCAAAT[A/T]CACACATAACAATAT | 93664 |
rs181466464 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122685067 | TATTTTTTTAACAGA[C/T]GGCAACTACATGTGG | 93664 |
rs181466892 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122369218 | CTCACTGCAAGCTCC[A/G]TCTCCCGGGTTCACG | 93664 |
rs181471340 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122792364 | GGCTCTAGGCCCCAG[A/C]GAGACCCCATCCCTC | 93664 |
rs181474780 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122348176 | TCAGTTCAGTCAGTC[A/G]CTAGACCTATCAGTC | 93664 |
rs181477643 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122853072 | AACCACAGTTAAGGA[A/C]AAGGCCTTGGCCTCA | 93664 |
rs181477745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122324447 | CATGTATTAGAACCA[C/T]CTGGAGGACTTGTTA | 93664 |
rs181477795 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122829469 | ATTATAAGACCAACT[C/T]CTCAGATTCCTACTC | 93664 |
rs181481342 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122812067 | TTTCATAGAACTTAG[A/C]AGATAGAAGTCCCAA | 93664 |
rs181490341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122874564 | GAACCAAAAGAGCTC[A/G]TATAGCCAAGACAAC | 93664 |
rs181494535 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122591003 | CTAACTTATCACCAT[C/T]ATTGTTGTTGACATA | 93664 |
rs181502808 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122606518 | ACACAAGAAAAAGAA[C/T]TGGCCCTTTATGGTG | 93664 |
rs181513042 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122571361 | TACCCGAGACAGAGG[A/G]AAACCTCTATTATTC | 93664 |
rs181522710 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122508064 | CACTACTTGTGTAGA[A/T]AATTTTATACACATA | 93664 |
rs181542291 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122733903 | CTATGATCACATCAC[C/T]GCACTCTAGTCGGGG | 93664 |
rs181553440 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122721383 | TCCCACAGAAATACA[A/G]ACTACCATCAGAGAT | 93664 |
rs181572173 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122841700 | AAAATCTCCACACAC[C/T]ATTAAATAACTAAAG | 93664 |
rs181575984 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122699757 | ATCTAGGGAAGCTAA[C/T]TTCTCTGCAGACTTT | 93664 |
rs181590150 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122405914 | ATGCTCACTGACAAT[G/T]ACACTGTTGGTGCTA | 93664 |
rs181591726 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | CADPS2 | GRCh38.p7 | 7:122338423 | AAACAAACAAACAAA[C/T]AAATAAATAAGTAAC | 93664 |
rs181593790 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122368935 | TGTGAGGACACCCAG[C/T]TGGTAACATAAGAAA | 93664 |
rs181600860 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122427714 | GGTGATGGCTTTGTA[A/G]CTTGTCTTAGATAAC | 93664 |
rs181607011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122445275 | TGAAATAGCCTTGGA[C/T]CCATAGGTCAATTTA | 93664 |
rs181607547 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CADPS2, LOC105375481 | GRCh38.p7 | 7:122529666 | CTTTTGGATGGCACC[A/G]TCTAAACAGCAGAAT | 93664 |
rs181608426 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122406170 | CTATGTGATTTCCCC[C/T]CCACCAGTTTTATCA | 93664 |
rs181613516 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122566458 | ATATAGAAGAGATAT[C/T]TGCACTCCAATGTTC | 93664 |
rs181615069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122547214 | GTTCAACCACAGGGA[C/T]GGTCTAAGAATAAAT | 93664 |
rs181619680 | snp | A/C | 0 | 0 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122532817 | ATTTTAATGGAAATA[A/C]ACCAAAATAACATTT | 93664 |
rs181623510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122474551 | ATGTACAGTATATTT[A/G]CTTTTCAGGCTTAAT | 93664 |
rs181627584 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122818114 | AAGGTAAGAACCCCC[A/G]AACCCCTTCCCTCCA | 93664 |
rs181632981 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122508739 | GATTCCATTAGGAAT[C/G]AATGGATGTGTGTTT | 93664 |
rs181634830 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122489302 | GAAAAGCAGAAGAAA[A/T]TAATGCATGTCAAGA | 93664 |
rs181646936 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122736239 | CCCATTGTATCTCCA[A/C/T]ATTTTCCCTTGTTTA | 93664 |
rs181657371 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122723013 | TCCCTTCCTTACACC[C/T]TATACAAAAATTAAT | 93664 |
rs181685157 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122842501 | TTTAACCACCACAAA[G/T]ACTTTGATGCTTAAT | 93664 |
rs181692894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122693041 | ACAGGTGGAGTTATA[C/T]GCCTGCACTCTAAAC | 93664 |
rs181697774 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122515137 | TTATATATTTTCTTT[C/T]AGCACATCAGCTAAC | 93664 |
rs181702583 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122579389 | TAGATAGAAAAGTTG[C/T]CTTTCTAGTATGAAG | 93664 |
rs181703551 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122712766 | TTAAGTAGATTTGGT[G/T]TCTCATGAGGGCTTG | 93664 |
rs181705395 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122552543 | ATACCCTACCCCCAA[A/C]TCAAGCCTTGTAAGG | 93664 |
rs181716258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122740167 | ACTTTGTAAAACAGG[C/T]TGATGGTTTCTTACA | 93664 |
rs181717338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122780909 | AAAAATCACTCTTAC[A/G]CATGTATTCTTATTT | 93664 |
rs181724422 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122427834 | TTTGATGGATACTGC[A/G]ATGAATTTATACATT | 93664 |
rs181725424 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122645117 | AGGCAAGAACATAAG[A/T]AGTTTAACCTCATAC | 93664 |
rs181731621 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122627159 | TCAGCCACTTATTTG[C/T]TATGTAATCATGGTG | 93664 |
rs181737246 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122594093 | TAAAAACACTGAATA[A/C]AATTTTTTATTATGA | 93664 |
rs181737898 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122801354 | TATTAAAAAAACTCC[A/T]AAAGAAATCTGTTAC | 93664 |
rs181741885 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122609489 | ATCCATAAATAACAG[C/G]AATTTTCTCCATAAC | 93664 |
rs181744134 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122518468 | TGTTATTATCATTTG[C/T]ATTCTGGACAATTGG | 93664 |
rs181748777 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122587886 | ATCTGTTGTTTCTTG[A/C]CTTTTTAATAATCAC | 93664 |
rs181757808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122601742 | CCCAGGAAAACAAAA[C/T]AAAACTTAAGAAAAA | 93664 |
rs181761188 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122555034 | CCTCAGGGCAAAGCC[A/G]TTCAGAAAGATATTC | 93664 |
rs181784888 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122886882 | GCGCGATGGCCCGTG[C/T]AAGCGTCCACCGGGG | 93664 |
rs181784944 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122455241 | AGTGCTTTCTCTACA[G/T]GTACACAAAATCATA | 93664 |
rs181786295 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122725855 | ACTGAAACAGGAAGT[A/T]CTTAAGAGCAAGGTA | 93664 |
rs181788312 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122419128 | ATATAGTTATCTTGT[G/T]CAGGCTTTGGACCAT | 93664 |
rs181789442 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122705795 | AATATATATCATATA[C/T]AATATAATATATATG | 93664 |
rs181794722 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122480014 | GAGACAGTGAAAACC[A/C]GGGTGTGTGCACTGC | 93664 |
rs181804921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122378389 | AGTGTCTTGCCTCAC[C/T]TGAAACTGAATGTTA | 93664 |
rs181805062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122678439 | GGCCACACAGAAGAT[A/G]GGAGTTATTACTCAA | 93664 |
rs181815016 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | CADPS2 | GRCh38.p7 | 7:122790120 | AATAGAAAAAGGCCA[A/G]GAGCAATGGCTCATG | 93664 |
rs181819332 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122358746 | GACCTTACAGCTTTT[A/G]AAGTTAATATTCACA | 93664 |
rs181820605 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122781427 | TTGTGTTTCTACTAG[C/G]CCCTAAATCCAAGAT | 93664 |
rs181823186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122555541 | TTTTAAGCCATAAAC[C/T]TGAAGTTTAGATATG | 93664 |
rs181823724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122740898 | ATGAAAACAAGCCTA[C/T]ATTCATAAAAAGAAT | 93664 |
rs181825335 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122759454 | TTTCAAAAGTACAAA[G/T]AGAAAACAATTGCCA | 93664 |
rs181841469 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122518765 | GGAACACACATTTAA[A/C]TGGGTTTTATGTGAC | 93664 |
rs181845212 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122681625 | CCAGATTTAGACCTG[C/T]GGGTGCTGCCCCACG | 93664 |
rs181847212 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122498394 | ATGACTATATCAATT[A/T]AAAAATCTTCCCATT | 93664 |
rs181863746 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122445859 | CAACTTAAATATTGG[A/C]GTGGAATTTTTTAGA | 93664 |
rs181864413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122707994 | ATTTAATGTGTATAA[C/T]ATGATGCTGTAAGGT | 93664 |
rs181868105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122480651 | TTGTGCCTGTATGAA[C/T]GGTAGATATTAGGTT | 93664 |
rs181871395 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122466262 | GATCCAGGAGTTGCA[A/C]AGTTTGAATGGAAGG | 93664 |
rs181880718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122759223 | TGACATCTTTCAGCA[C/T]CCACCTGAAAGTCAG | 93664 |
rs181894889 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122652517 | ATTTGAAATTAACTG[C/T]ATTTCCTTAAAATAT | 93664 |
rs181917101 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122619631 | GACTCAGTCTCCAAA[C/T]AAATAAATAAATAAG | 93664 |
rs181921501 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122836476 | TCCAATTAAATGACA[C/T]AGACTGGCAAATTGG | 93664 |
rs181927100 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122435595 | ATTAGGTGCAGCCAC[C/T]ATGAAAAATAGTATG | 93664 |
rs181929794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122875151 | TACACGTTTGCAGAT[A/G]TGTACATACGTGTTT | 93664 |
rs181931386 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122473440 | AGGTTTTTCTTTTAA[C/T]AAAGCTCAAAGGAAA | 93664 |
rs181932709 | snp | A/C/T | 0.0234234 | 0.105655 | intron-variant | CADPS2 | GRCh38.p7 | 7:122575178 | TCATTATAATAAAAG[A/C/T]AAAAAAAAAAGGTGG | 93664 |
rs181933673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122728887 | CCCAAGTATTTATTA[C/T]ATTACAAGTCGCCTC | 93664 |
rs181935919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122406574 | CTCCAGAAGAACACT[A/G]AGAAATGGAGTGAGG | 93664 |
rs181937908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122763351 | TAGTGTGATGAGAGT[A/G]CTGAATCCTACTCCA | 93664 |
rs181938216 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122744860 | CATGGCATTGTCTGG[C/T]GTGGGCAGGGAGCTG | 93664 |
rs181944180 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122370176 | CTAAATGAGTTACTC[A/G]GTCACAGATTATCCT | 93664 |
rs181960494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122325833 | GCTGTAACATATTCA[C/T]GGAAACAGTGTTTTT | 93664 |
rs181960939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122653059 | AAGGATATTACCAAA[C/T]GATGGCCATCGATGT | 93664 |
rs181963967 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122689507 | AACAGTTATTGCTAA[C/G]GGATAGAACCACAAG | 93664 |
rs181967252 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122768922 | AAATGTAGATAACCT[A/G]AAAGACAGCATATGC | 93664 |
rs181967948 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122638107 | AGGTTTGCTCCTAGG[A/C]CTTGGAGGAGCCCCT | 93664 |
rs181968114 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122503248 | GCCATGCTGGCCAGG[C/G]TGGTCTTGAACTCCT | 93664 |
rs181975794 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122541887 | TATATTTATATATAT[G/T]CATATATATTTATAT | 93664 |
rs181977341 | snp | A/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122522797 | ACAGATCAACTTTTT[A/T]AGCTTTTACATGTGA | 93664 |
rs181978105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122716915 | TGGGGTTTTGTCCCT[A/G]CTTGCAATGTGAACA | 93664 |
rs181981418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122803315 | GTTCTGTAAAGGGAA[A/G]TCACAATTCAGAAAG | 93664 |
rs181985456 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122682258 | AAAATCTTGTTGTTC[A/T]TCATGGAAAAGGGAG | 93664 |
rs181988005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122440437 | CTGAGTTATGTGCAG[C/T]TTTCAGTATTATAAA | 93664 |
rs181992999 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122403098 | ATTCACTAAATAACT[A/C]AGTATCTAAGGAATG | 93664 |
rs181993074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122449429 | CAAGTGATCCTCCCA[C/T]ATCAGCCTCTGGAGT | 93664 |
rs181993220 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122483657 | ATAATAGCAATGTAT[A/T]GTGGGATTTACCACA | 93664 |
rs181995007 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122424511 | GTCAGATACATGTGA[A/G]GTAAAAGTCAGTGAC | 93664 |
rs181995257 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122668699 | AGAGAAATAGAGAAT[C/T]ATCAAGTACCATAAG | 93664 |
rs181995389 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CADPS2, RNF148 | GRCh38.p7 | 7:122702871 | AAATGGAAAAGGTCT[A/C]CCTGGATCAAAGCTA | 93664 |
rs182000267 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122469450 | ACAGAGTCAGGAGAC[A/G]AGACAGTTTTAGTAA | 93664 |
rs182000447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122384717 | GAACTAATTGTCTCT[A/G]GTGTGAATGTACAGG | 93664 |
rs182001067 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122609996 | AGCATTCATGAGATA[A/C]CTTTTTAAGGTAATC | 93664 |
rs182013161 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122364073 | ATCATGCTACAGAAC[A/T]GTAAGAATTAAGTGA | 93664 |
rs182017705 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122344105 | CAGTGAACACTGACA[C/T]GAGAGACCACGGCAG | 93664 |
rs182019388 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122834684 | CACGGAGCCTTGCTC[A/G]CTGCTAGCACAGCAG | 93664 |
rs182021344 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122537030 | TTTTTGAGGGTGGAG[A/G]ATGGGAGGAGGGAAG | 93664 |
rs182023849 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122849291 | AAAATATCTGGAGGA[A/G]ACTATTTTTTCACTT | 93664 |
rs182024857 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122645359 | CATGTGTGTGTATAC[A/G]TGTACATGTATACAC | 93664 |
rs182025672 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122864314 | TGTCATACACCAAAA[A/C]TACAAAAAAAATAAA | 93664 |
rs182025934 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122871144 | CAAACAAAGGAAGAC[A/C]GGGGACAACGGAGGA | 93664 |
rs182039721 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122575727 | CAAGCATGAGCTACT[A/G]CACCTGGACAGAAAT | 93664 |
rs182042467 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122497994 | GACATCTCACTTGGT[A/G]GCCCAGGTTGGAAGG | 93664 |
rs182048299 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122465872 | GAAAGTAAAATAACA[A/G]GCCAATTTTGTACGT | 93664 |
rs182052970 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122436230 | CACAGCTATTTACCT[C/T]CAAATTCATCAAGTT | 93664 |
rs182076557 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122696560 | TACCTGTGTCTGAAT[C/T]GCAGTATTGTTAACA | 93664 |
rs182084300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122511409 | CCTTACCTGGCAAAA[A/G]GCATGAGGTGATCAT | 93664 |
rs182099564 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122667932 | GAGTGGGGGCCACGT[G/T]GGGGGAGGGAGGACT | 93664 |
rs182102400 | snp | C/T | 0.0948562 | 0.196037 | intron-variant, nc-transcript-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122530331 | TTTTTTTTTTTTTTT[C/T]CCCACTAGCTTTCAA | 93664 |
rs182103819 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122507687 | CTTTAAATAGATTAT[A/C]CCACAATGTGAAGAA | 93664 |
rs182111174 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122613033 | ACATTACACCATATA[C/T]AAAAATCAACCTAAA | 93664 |
rs182111733 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122491479 | TACCAAATTTAACTT[C/T]CGTTTTTTTATCAAA | 93664 |
rs182114037 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122457193 | ATCTAAGAGAAAAAG[A/G]GTACAAAACTGGGCT | 93664 |
rs182116615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122474945 | AACACACATGCTTCA[A/G]CTGGATCACTTCCAG | 93664 |
rs182123541 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | CADPS2 | GRCh38.p7 | 7:122723905 | AAGCTGGAAACCATC[A/G]TTCTCAGCAAACTGT | 93664 |
rs182153747 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122786078 | TTTTATTGTTACCAC[A/T]TTCAGATCTTCTAAC | 93664 |
rs182162839 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122821641 | TAGCCTTCCCACCTC[A/T]ATACAGTCTGATAAC | 93664 |
rs182168940 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122755263 | AGCAAACCATGCTGA[C/T]GTCTTTCCTTAATAA | 93664 |
rs182176328 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122755601 | TACATAAAATGAATC[A/C]CCAGATGTTAAAAAT | 93664 |
rs182178618 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122674744 | CTGCTTGCCAAATCA[C/T]TGTGGCTATGAGATG | 93664 |
rs182185364 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122637375 | ATTTCTTGTAGAGAA[A/C]AGGAGGCTGACCTCA | 93664 |
rs182195021 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122737746 | AATTAACTAATAGTT[A/C]ATATTAATAATATTA | 93664 |
rs182205230 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122516416 | AGTGGTACACACTTG[A/T]CTTTGCTACTTGGGA | 93664 |
rs182206047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122853700 | TTTAAATCTTGAAGA[C/T]ATGCATACATTGTTC | 93664 |
rs182207291 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122697054 | AGAAACACATGGGAA[G/T]TAAATTTGCCATGAC | 93664 |
rs182211495 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122495577 | GTCCTTCACTTTTTT[C/T]CACTTGTCCTTACAA | 93664 |
rs182212692 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122387468 | ATTTAATGGAAAAAA[A/C]ACTCATAATTTCACT | 93664 |
rs182217273 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122454173 | CATCTTGTCACTGTA[A/T]TTATTAAAACAAACA | 93664 |
rs182222768 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122533315 | ACAAATCTCTTTAAC[A/G]ATTAATAATTGTCTT | 93664 |
rs182224932 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122418129 | GAGCCAATATCACAC[C/T]ATTGCGCTCCAGCCT | 93664 |
rs182231330 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122460886 | AGATGTCAGAGCTGA[A/C]GAGAGAACTGAAGAA | 93664 |
rs182234859 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122415532 | TGGAATTATGAGAGA[A/C]ATAGAGTGAGATTTC | 93664 |
rs182235988 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122494987 | GTTAAGGGGTTGGAG[A/G]TGGGGGTGTTGAGAG | 93664 |
rs182240994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122461597 | GCCTTTTTTGTTGTT[A/G]TTTTGTTTTGTTTTT | 93664 |
rs182241080 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122477960 | ATCTTTCACTTTAAA[A/G]TTATCTCATGAACTA | 93664 |
rs182249567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122424721 | TTCGGCCCAATTTGA[A/G]TTTTATTAAAGTTGT | 93664 |
rs182250479 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122376934 | TATGGAGATTAATTT[A/G]CATCATCTTTTTAAA | 93664 |
rs182251633 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122395574 | ATGCCACCTAAATAA[G/T]CATGCTAAACTTTAA | 93664 |
rs182252260 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122682964 | CTGGAACAAACGATT[G/T]CTGGAACGGCCAGTT | 93664 |
rs182253669 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122441045 | AGGTAACACATACAC[C/T]GGAATAATTGAAAGA | 93664 |
rs182253883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122808598 | ACTGTCTACTTCTTA[C/T]ACATAAATTGAAGTT | 93664 |
rs182257075 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122839477 | CAAAAGAAACTACCA[A/T]CAGAGTGAACAGACA | 93664 |
rs182260316 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122647446 | GTAGGCAATGAAGTA[A/G]TTTTAGACATTTAAT | 93664 |
rs182261598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122356203 | CCTTGGACTCCTCTT[A/G]GTTGTGTCACTTTCT | 93664 |
rs182264524 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122860590 | AGAACCCCCAAGGAT[A/G]AAGAACATTAAAACA | 93664 |
rs182266760 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122630902 | TAAATCCTTGTTATA[C/T]AGGAGTTTCTATGTC | 93664 |
rs182267126 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122335416 | ACCACACCCGGCTAC[A/T]TTTTGTATTTTTAAT | 93664 |
rs182269567 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122668899 | CTGTTTTTTGTTTCC[A/G]CATATAACATCATCT | 93664 |
rs182275844 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122881170 | TACTTTGTAAAAGTA[C/T]GAATGAAGAGAGCTG | 93664 |
rs182282431 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122724189 | TAATAATAATTGAAA[A/C]ATTAAAAAATAAAAA | 93664 |
rs182283786 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122818677 | TTTTTATCACCTCCC[C/G]TCCTCACACCTGGTC | 93664 |
rs182292335 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122709683 | CAATGATAGACTGGA[G/T]TAAGAAAATATGGCA | 93664 |
rs182293570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122430897 | CAATGGAAGAGAACT[A/G]TGATGATGGAAGAGA | 93664 |
rs182294841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122661769 | CCTAATACCTACAGA[A/G]GTTTTGGACTTGAAT | 93664 |
rs182296646 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122797597 | AAACTAATGCAGGAA[G/T]GGAAAACTAAATACC | 93664 |
rs182304444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122391580 | GCAATTTTCTGAGCA[C/T]ACACAGACACCACTT | 93664 |
rs182321898 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122628409 | ACTGTAAAATGAAGA[C/T]GTGTGCAGTTTATTG | 93664 |
rs182327933 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122594469 | AGCTAGTTCTCATTT[G/T]GTTGCTCTAAGGATT | 93664 |
rs182331706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122353507 | CACAGTAATCTTTAT[C/T]GTATCCTCCAAGTCT | 93664 |
rs182348229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122604248 | CCTTTCCTAACTTAT[A/G]TATATCACCATTGTT | 93664 |
rs182379813 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122488030 | AAATGAAAAACACAG[A/G]AAATTCACATTAAAT | 93664 |
rs182381815 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122638328 | AGGGCGTCCTCCCCA[C/T]CCCCTGCTTGGGGCT | 93664 |
rs182383835 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122568466 | ACAAAACTATAGCAA[C/G]ATATTTCAATACCTA | 93664 |
rs182384945 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122649733 | TACCATTACATTTCA[C/T]ACATCTATATGATTT | 93664 |
rs182389775 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122528044 | TGGGGTCATTACAAA[A/T]ATCTGCTGCAATGAT | 93664 |
rs182402042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122634457 | TTCTATGTAGCATAT[A/G]CAGAGGTTTTCAAAA | 93664 |
rs182405648 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122736895 | TGAGAAACCCATAAA[A/G]ATAATAAAACTCCTT | 93664 |
rs182411924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122617810 | GCACTTTGGGAGGCC[A/G]AGGCGGGCATATCAT | 93664 |
rs182417235 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122718623 | TAACAAAGCTTAGTG[A/T]AATGAGGATACAAGA | 93664 |
rs182417850 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122708372 | TGATCATTTCAGTAA[A/G]AGTATAGGATAGTTA | 93664 |
rs182422283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122805981 | GTTAAGTAGGAGGTA[C/T]GGATTTTTATATGTA | 93664 |
rs182423249 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122679194 | CGAAAACAGGTAAGA[A/T]AAATATCACTGAATT | 93664 |
rs182429641 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122665978 | TAACAATATGTTTTG[C/T]CTAAGAATGACAAGA | 93664 |
rs182435918 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122776676 | GGAAGATGTGGGAAA[C/G]TTTAGAATTTCCTAA | 93664 |
rs182441848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122561889 | CCAAGTATTTGTTGG[C/T]TGGATGATTGGCTGG | 93664 |
rs182442078 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122583685 | TACGTGTGTATATAC[A/G]TATATACATATGTCC | 93664 |
rs182449431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122499256 | TTTATAAGATCTCTG[C/T]TCCAAATACCCACTT | 93664 |
rs182452524 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122659725 | GAATTGCAGAAAAAT[C/G]AAAGAAGGAAAAACT | 93664 |
rs182453817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122553708 | GGGCCCTAATGCCAG[C/T]AGACTCTGCTTGTTA | 93664 |
rs182454741 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122599704 | TTCTTTCTAAACTTG[A/C]AAGCTATTTCTTTGT | 93664 |
rs182457747 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122571979 | TCACTTTAGGCCTTT[C/T]CTTAACTCTCACAGA | 93664 |
rs182477944 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122533637 | GAAATATCCAGAAGT[C/G]TCATGTTATTTTATG | 93664 |
rs182480371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122516920 | TATTGGTATAGTTTA[C/T]ATAAAGTAAAATTAC | 93664 |
rs182487846 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122477459 | AGGCGAAGGTTGCAG[C/T]AAGCTGAGATTGCGC | 93664 |
rs182491283 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122777396 | AACAAGAGAAAAAGG[C/T]GACACCTTGTAACTT | 93664 |
rs182494158 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122719391 | CTATCTGACTATCCC[A/C]CTATCCTTCTGTTAA | 93664 |
rs182495465 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122799273 | TCTTTTCTTTCTAGA[C/T]TGAGAGAAGACAGAA | 93664 |
rs182498593 | snp | A/G | 1.65638e-05 | 0.00287778 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122393518 | CATGAGATCCACATA[A/G]CGGACAACCAAGGGT | 93664 |
rs182502271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122778111 | TGGCTTTGACCAAAA[C/T]GCTGATAGTGATATG | 93664 |
rs182503668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122414501 | ACAAAACATACATAT[A/G]TTTTATCACATAATC | 93664 |
rs182507596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817535 | CTTGGTGTTTAATCA[C/T]TGCAGGGACGCCTCT | 93664 |
rs182511823 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122345738 | TCTCAATTGTGAAAT[A/T]ATTATTTAATCATAC | 93664 |
rs182515555 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122375357 | CTTTTTTAAGTAAAC[A/T]TTTTAATGTAAACAA | 93664 |
rs182517082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122320930 | TTGAAATTCCCTTGG[A/G]ATGTGAAGTGCCAAA | 93664 |
rs182517555 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122748384 | CCTCAGTACCATCTG[A/G]CATTTCATGGCACAG | 93664 |
rs182521034 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122355130 | TGGTTTGATTTGGGT[A/C]ATTTTCTGTTAACTC | 93664 |
rs182521791 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817069 | CCACCCATATCTCCC[C/T]TCGCTAACTCTCTTT | 93664 |
rs182524790 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122851212 | AAGGTGCAGGTGTGA[G/T]GTCTACAGAAGGAAA | 93664 |
rs182524941 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122835425 | AGCAATGGAACAAAG[A/C]TGGATGGAGAATGAC | 93664 |
rs182537154 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122872635 | TGTAAGCCTTTTTAA[C/G]TAAGCAGTATTTTTA | 93664 |
rs182558822 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122837765 | AGACCAATAACAGGC[G/T]CTGAAATTGAGGCAA | 93664 |
rs182560506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122691630 | ATGAGGCTATGCATA[C/T]AGTCCTGCAGTGACA | 93664 |
rs182566250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122756251 | TGGTATGTACCAAGT[C/T]TATGAATTCAAAACA | 93664 |
rs182572091 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122412590 | AACTGAGAGCTGTCT[C/G]CATTGCAAATACCAA | 93664 |
rs182575554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122374368 | ACACTTACCACTTCT[A/G]TTCAACATAGTACTG | 93664 |
rs182579079 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122738240 | GCAAAATAAAAATAA[A/G]GAGCTTCTTAGTAAA | 93664 |
rs182594591 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122486536 | GATAAGAAGTTGGTT[A/C]CTTTGGGTGAAGCAA | 93664 |
rs182601795 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122332443 | CATGTGATTCATGCT[G/T]CTTTTTTCCATGTTG | 93664 |
rs182602517 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122607418 | CCTTCCAAATTTAGA[A/C]CACTCACTAATTTGT | 93664 |
rs182610643 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122625340 | TAGGCATGAGCCACC[A/G]CATCTAGCCCAATTA | 93664 |
rs182611080 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122452188 | CAAATAACAGAAATT[A/T]AGAATTTATTCTGTA | 93664 |
rs182613984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122620288 | TTACTATTTACTCAC[A/G]GAATAAAAATCATGG | 93664 |
rs182623337 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122421616 | TGAGGGGATACAATG[A/T]TTAAAAAGATATTAT | 93664 |
rs182631975 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122436966 | GTTTTTTTGGGTAGA[A/G]TACATAACATTTACA | 93664 |
rs182634993 | snp | C/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122400091 | AGCCACTAAACCCTA[C/T]GAAAATATAAAAAGC | 93664 |
rs182647384 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122588739 | TGTCCTATGAGAGAT[G/T]TGCTGAAGAAACTGA | 93664 |
rs182649763 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122877725 | CGTATGCTCCTAGAA[A/G]GCTGAATATAGTAAA | 93664 |
rs182651025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122385148 | TAGGAGCCACTGGTA[C/T]CTAAGCTAGCTGCCT | 93664 |
rs182660515 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122450230 | AGAGCATATTCACTA[A/C/T]GTTTATTTTTTAAAT | 93664 |
rs182666684 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122345054 | AAGGCACCCCGCCAT[C/T]CCCCCGGCCCACACA | 93664 |
rs182673285 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122433244 | CCTCAGCCTCCCAAA[G/T]TTCTGGGATCACAGG | 93664 |
rs182682021 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122549305 | CTTACTGTCTACATG[A/G]CATTTATTTTGTAGT | 93664 |
rs182686946 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122680079 | AGATTTCTCTGTCAT[A/G]ATCTTTGCAAAGGCA | 93664 |
rs182691597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122666615 | CCAAAGTGCTGGGAT[C/T]ACAGGTATGAGTCAC | 93664 |
rs182702182 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | CADPS2 | GRCh38.p7 | 7:122721637 | TGGTACCATTCCTTC[C/T]GAAACTATTCCAATC | 93664 |
rs182714951 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122760077 | TTACACACAGTCTAT[A/G]CTAGAATCAATATGT | 93664 |
rs182716129 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122694483 | ATATGCATGGCAGCA[A/T]CTAAAAATCATCACG | 93664 |
rs182717769 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | CADPS2 | GRCh38.p7 | 7:122706300 | GAATATATATATGCT[C/T]ATATATTCAAGGAAT | 93664 |
rs182723092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122607763 | TGCTTATCTCTTTAG[A/G]CTTCATTTTGTTCTG | 93664 |
rs182728626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122626043 | AGGCAAGGAGGCCAC[C/T]ATCGCCAAAGTGGAT | 93664 |
rs182731698 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | CADPS2 | GRCh38.p7 | 7:122320014 | TCTTGGCATTTCCCC[C/T]TTTACTCTACATTCA | 93664 |
rs182740894 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122731095 | GGCAACAACAAAGCT[G/T]ATTTTAATACTTTTT | 93664 |
rs182743878 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122525285 | AGCAGAGCTCTGAAA[A/T]TTAGTAAACAAACTA | 93664 |
rs182744369 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122650062 | TACATGCGCGTGCCA[C/G]CACACCTGGCTAATT | 93664 |
rs182748737 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122704636 | AAGGACCAATTTGAG[G/T]AACTTAGCTCATTCA | 93664 |
rs182749414 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122552756 | AATTAGGGTCATCTC[G/T]GCACTATGATAGGTT | 93664 |
rs182758775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122766437 | ATACCGATAAGAATA[C/T]TTCTACATTTCTAAT | 93664 |
rs182766491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122797780 | CTAGGAATAATACCC[A/G]GTTTGACAAAATAAT | 93664 |
rs182773565 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122365547 | TGTTGGGTTTAGTTG[C/T]TGCATCTTTAACTGC | 93664 |
rs182809198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122334221 | ACACACACACACTCA[C/T]TCACAAAGCTATGCT | 93664 |
rs182809979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122371058 | AACTACAAGGAATAC[A/G]GTGTTCCCCAAATGG | 93664 |
rs182815272 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122350620 | GATGGAAATACACAG[A/C]GATTACAGAGCCTTC | 93664 |
rs182818369 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122734571 | ACTGTTCTGGTAAAC[A/T]ATAAAAATTACTACA | 93664 |
rs182819621 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122710692 | TAAAATTCCCATCAT[A/C]TTTACAGACCCATTT | 93664 |
rs182822621 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122326822 | ACAAGAAATGGTATT[C/T]TAAGTATAAATTAAA | 93664 |
rs182824820 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122753470 | CTCAGCAAATATTTA[C/T]TGAGAACCTACTACA | 93664 |
rs182828072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122654181 | TGAGGAAAAAGGCAA[C/T]AAGCCATCTCCATAA | 93664 |
rs182844283 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122676197 | TGAATAGGTTCCTGA[A/C]TGATTAGTCTGTTTA | 93664 |
rs182847436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122673123 | TCAGGAGTGAAGTTG[C/T]AGACCTTCGCTGTGA | 93664 |
rs182854890 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122657490 | TTTATTTCGTTGAGC[A/T]GTGGTTTGTAGTTCT | 93664 |
rs182856559 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122472065 | TCTTCCTATGAACAA[C/T]ATAACAGAGTTAATG | 93664 |
rs182862225 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122642464 | TCCTAGGGAGAACTG[A/G]AAGCCTGTGCTGGCA | 93664 |
rs182867883 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CADPS2, RNF148 | GRCh38.p7 | 7:122701334 | TCTCAGCGAACTATC[A/G]CAAGGACAAAAAACC | 93664 |
rs182869558 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122505364 | AGACAATTATTTTTT[A/T]AAAAATGCTAGAGAT | 93664 |
rs182870071 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122354392 | GAGCAAGGATTCAAC[C/T]GCCAGCAGTTCGGTT | 93664 |
rs182872963 | snp | C/G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122714526 | TGGGTAAAACAGTTA[C/G/T]AAAAAGAATCCATAG | 93664 |
rs182876968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122687359 | TGCATTTCTTTAAGC[C/T]CTTAAAGCTGGACTC | 93664 |
rs182877248 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122581842 | AAGAATCTGAATGTT[C/T]TGTAGTTAATTTCCC | 93664 |
rs182879217 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122434422 | GCTTATAACATTGCA[A/T]ACAAAATTTGACCAA | 93664 |
rs182894434 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122821584 | GTCTGAGATGGCCAC[C/T]GCAGTCATTTCTTCC | 93664 |
rs182903410 | snp | A/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122544021 | TTGAAAAAGTTTTGT[A/T]TTATCTTGTAAAGAT | 93664 |
rs182912890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122523801 | TAAAGAAAATTAGTA[A/G]GCTTTCCAAGCTGAT | 93664 |
rs182921754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122561594 | GGCAAGCCGTTAGTA[A/G]TCTACGCTCCTTGAG | 93664 |
rs182926284 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122404014 | TTTTTTATTATACTT[A/G]AAGTTTTAGGGTACA | 93664 |
rs182927303 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122484663 | CATCAAAATTAAGAA[C/T]TTCTTTTTTTTTTTT | 93664 |
rs182929421 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122463591 | GGGAAGTTACAGCCC[C/T]AAACTCTTAGAAAAG | 93664 |
rs182933106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122471631 | TTGCTTTCCTGAACG[C/T]ACTTTTAGGCCTTAT | 93664 |
rs182933901 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122364808 | CATACAAAAACACAA[C/T]AGTCTTAGATCTTTC | 93664 |
rs182938901 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122504419 | AGTATAGTCAGCACC[C/T]GATTGACTTGGGGAT | 93664 |
rs182941249 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122443309 | AACTACATAGAAGCT[A/T]AATTAATCTTTACAA | 93664 |
rs182952866 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122839664 | CATTTATGCAGCCAA[A/C]AGACACATGAGAAAA | 93664 |
rs182963150 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122478324 | AACTATCAAAACAAA[C/T]CAACAAGCTATGAGC | 93664 |
rs182966087 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122442948 | TGGTGCTTTTAAGAG[C/T]ATTAGCAAATTAGCA | 93664 |
rs182969191 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122881745 | TGCTAGAAACATCAG[G/T]AAAGTGTTACTTTGA | 93664 |
rs182972152 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122753829 | TACTCACCCACTGGG[G/T]TGTTGCATATTTCAC | 93664 |
rs182974580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122694191 | ATGACTTACAATTGC[C/T]TCTAGGCTGAAGCTG | 93664 |
rs182976456 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122660573 | AATGGCCTAAACATA[C/T]CCATTAAAAGACCAA | 93664 |
rs182979714 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122774169 | TTAATCTCTAAAAGT[A/C]TAAATTATTGAAAGT | 93664 |
rs182985283 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122645679 | TATATATATATATAT[A/C]TATCTTGGGATTTTG | 93664 |
rs182993272 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122703389 | GATGGTTCAACACTA[A/C/T]CCAGTATGGCATTCT | 93664 |
rs182995031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122605035 | TATAGCATGTATTGT[C/T]CTAAATACTGTAGAC | 93664 |
rs182995499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122404151 | TCCCCCCTCTCCCCA[C/T]CCCATAACAGGCCCC | 93664 |
rs183004656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122858614 | CCATATGTGTTTCAT[C/T]GCTTGCTTTTAACCT | 93664 |
rs183005983 | snp | C/T | 0.00140666 | 0.0264831 | missense, upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122621710 | ATAAATTTGGGGAAT[C/T]TTCTTTCCTTGAAAA | 93664 |
rs183006183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122690534 | AGGGGCTTGGAGGGT[C/T]CATGGCTGACACCAG | 93664 |
rs183011041 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122675666 | GAGTTCATGTCCTCT[A/G]CAGGAATGTGGACGA | 93664 |
rs183015227 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122550152 | GGCCACAAAGCAGCC[A/G]GTGTGGGGCTTGTCT | 93664 |
rs183021436 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122700810 | TAGCTGAGTCACTAT[G/T]CTAGGATTTAAAGAG | 93664 |
rs183028948 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122571812 | ACTGGACCACGGAAT[A/T]AAAATTTTTTCTCTA | 93664 |
rs183038314 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122589232 | TCCCACCTTTACTAA[A/T]AAACAGTATTATCTC | 93664 |
rs183039691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122629510 | TAGATTGGCAGACCA[A/G]ATAAATTTCTTGGGT | 93664 |
rs183041255 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122511965 | ACCCCAAACAGGTAA[A/C]CTTTTTCAAAGCAAA | 93664 |
rs183043526 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122726297 | CAAAATTAAATTTTA[A/T]AAACAAAACCAATAG | 93664 |
rs183052406 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122544339 | GCATTTGATGTATAA[C/T]AGAAAAAATAAATTG | 93664 |
rs183054903 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122530953 | AAAGTGTTCACATGT[A/G]TAGAATGCCATCCCT | 93664 |
rs183061302 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122618165 | ATTGAACAGCTTAGC[A/G]TTTTGTGGATTGGCT | 93664 |
rs183063587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122812352 | GTAGAAAACAAATAT[A/G]AAAAAATTTAAATGT | 93664 |
rs183063709 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122467201 | GCTTATGACCTTTCA[C/T]CTGGTTGCTCACCTG | 93664 |
rs183067118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122428688 | TGGTCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 93664 |
rs183067926 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122399523 | AATATTAAAGGCAAA[C/T]AGAAAAGTCTGTAAT | 93664 |
rs183069859 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122381295 | GGAAATTAAATGCCA[A/C/T]GTGATACACCTCTTT | 93664 |
rs183077500 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122446674 | ACAGGAGACTCCAGG[A/G]AATCATTTGCAAATA | 93664 |
rs183080005 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122843337 | GACTTAATTACACTT[A/G]TATCTGCCACAGTGG | 93664 |
rs183082033 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122795736 | GAGCCATCTATGACA[C/T]ACCCACCACAAACAT | 93664 |
rs183082773 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122782917 | TATATTGACTCTATT[G/T]AATGACTCATTTTGC | 93664 |
rs183082987 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122830181 | AAGGTCTCTGGATCT[A/T]AACCAAACACCACAA | 93664 |
rs183087363 | snp | A/C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122408999 | GGGGACATTTTAATG[A/C/T]CTGGCTCAATGCTGT | 93664 |
rs183089237 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122339883 | AGAGTGAAACTCCAT[A/C]CAAAAAAAATAAAGT | 93664 |
rs183091796 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122672398 | GCACCATGCTGGTGT[C/T]GAAGCTGTCATGGGA | 93664 |
rs183093535 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122372175 | CTAAGATCAGACAGC[G/T]AGTGGAGGAGTTGAA | 93664 |
rs183094027 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122865124 | CCGTGAGGGATGGTT[A/G]TTAAAATGAGTCTGG | 93664 |
rs183094805 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122389152 | CGTTATTCATGCATA[A/T]GTGCCTCTGTCACCA | 93664 |
rs183095473 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122887327 | TTGGGATGCAGTTGA[C/T]TCAAAACAGGTTGTG | 93664 |
rs183096565 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122814153 | CAAGCTATTCTGGTT[C/T]CTATATGATAACATG | 93664 |
rs183096635 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122855307 | GAGAGGTACTATACA[C/T]ACATTAATTTATTTA | 93664 |
rs183099925 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122585507 | AAAGAAGACAATAGG[C/G]CTACCTTCAATATTC | 93664 |
rs183103970 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122875891 | GAACCACTCTCTCAC[A/G]TCTCTCTCCCATTCC | 93664 |
rs183105414 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | CADPS2 | GRCh38.p7 | 7:122832883 | CTGCTGGCTTTTTTT[A/T]AAAAAAGACAGCTTA | 93664 |
rs183106032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122641794 | TATACCTACAGTACA[A/G]CATACCCTGTTGCAG | 93664 |
rs183106867 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122846631 | AAATATAGGAGCCAA[C/T]AATTTTAAGGAAGAG | 93664 |
rs183106904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122351658 | GGCTGTTCCATTACT[A/G]CAGAGTTCTTGTCCT | 93664 |
rs183110174 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122466640 | AGCTCATTTAACTAA[C/T]ACACTGCATAAAAAA | 93664 |
rs183114321 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2, RNF148 | GRCh38.p7 | 7:122701428 | GGGAACGTCACACAC[C/T]GGGGCCTGTTGTGGG | 93664 |
rs183121103 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122825202 | ATTGTGGCAAAGTTA[C/T]AAATATGTTTACTGT | 93664 |
rs183121825 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122865312 | TCTTACCTTTATAAA[C/T]TGCCCAGCCTCAGGT | 93664 |
rs183138450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122428323 | CACTGTATTCTTTAA[C/T]ACCATGCACTCAAGT | 93664 |
rs183139085 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122742198 | GAGTTCGAGACCAGC[A/G]TGGCCAACGTGGTGA | 93664 |
rs183140549 | snp | A/G | 0.00101091 | 0.0224596 | intron-variant | CADPS2 | GRCh38.p7 | 7:122388573 | CAGCAATTTGAAAAT[A/G]CATGTCTACCTTTTG | 93664 |
rs183142745 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122361490 | ACCCGCCTTGGCCTC[C/T]CAAAGTACTGGGATT | 93664 |
rs183147071 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122715142 | AGCTAATAGAGCTTA[C/T]TGGTCATTTAAGTTT | 93664 |
rs183153299 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | CADPS2 | GRCh38.p7 | 7:122726815 | ATAAGATAGAGTTTG[C/T]TTGAATGAGGTGGAT | 93664 |
rs183162489 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122724446 | TCACAAAGCAGTACA[C/T]ATGATAATATAAATT | 93664 |
rs183203227 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | CADPS2 | GRCh38.p7 | 7:122495846 | ATTTTTTGCCAACTT[G/T]GATGGGTGGGAAGTG | 93664 |
rs183214200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122795079 | AGAACCAAGAGCAAA[C/T]AAATCCCAAAGCTAG | 93664 |
rs183217547 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122831339 | GGTGTTTTCGCTCAA[A/C]TGGAAATGTAACCCT | 93664 |
rs183225792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122462485 | GGTAGAAATGGATTT[A/G]CTTTTATTAACATGT | 93664 |
rs183234644 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122860690 | AGGATTTCTCTTATA[A/T]AACTGTAATTTTATA | 93664 |
rs183234981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122419937 | ATTTAACTTATTTTA[A/G]ATCACTGAAGTATAT | 93664 |
rs183241405 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122704060 | ATAGGTTATCTTCTA[C/T]GTGCTCAGCATGCCA | 93664 |
rs183252293 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122665330 | ACTCACACAAACTGT[C/T]TTTCTTGTTTCCTAT | 93664 |
rs183254159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122534606 | CAAGACCCTAATATT[C/T]AGAGTTTGTAAATTA | 93664 |
rs183260039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122598531 | CGTACAATGTCACTT[A/G]GCAGATTGTATTTAA | 93664 |
rs183261733 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122425261 | GCTGGGATTACATTC[G/T]TGAGCCACCATACTC | 93664 |
rs183267450 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122730034 | AGTGAATATTGGAGG[A/T]AAGAAACTTACAAAA | 93664 |
rs183274548 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122747413 | TACAAATAATTCCAG[C/T]GGACTATGTCAAATT | 93664 |
rs183274861 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122633525 | TGTATAGAAGTTCTA[C/T]TGATTTTTGTACTTT | 93664 |
rs183277442 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122718973 | CACCTACTGTTTTGA[A/T]AATAAAACTTTTAGG | 93664 |
rs183285059 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122713956 | GCTCTGCTGGCACAA[C/T]ATTTTTCAATATGTT | 93664 |
rs183287784 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122572362 | GACTTTATAGTTTTA[C/T]CTATGCTTTCCCCAT | 93664 |
rs183290932 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122496306 | AGCTGGGATCACAGG[A/T]GTGCGCTACCGTATC | 93664 |
rs183291974 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122687130 | TTTTTACACAAGGGA[A/G]CTACTAGCTCCAATA | 93664 |
rs183294271 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122540482 | TGTTGTGGGTATGCT[C/T]CTCAATTTGGAACTA | 93664 |
rs183297600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122588467 | GTAATCCTTTCCCCA[C/T]TGCTTGTTGTCAGGT | 93664 |
rs183301756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122558108 | TTATTGAAATGTAAC[A/G]ACTTTCTTGTTATAG | 93664 |
rs183304089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122603414 | CTTAAAAATAGGATG[C/T]TAAAAGAAGAGATTT | 93664 |
rs183311302 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122482922 | AGGGAAAGAAGCAAT[C/G/T]TAAAGGATTCGAGAG | 93664 |
rs183315137 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122740948 | GAAGCCATTTTAAAG[C/G]TACATATCCTTGGAA | 93664 |
rs183323031 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122501256 | TGAACTCTGTCTCAA[A/C]AACAAAACAAAAAAA | 93664 |
rs183330219 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122448004 | AAACTATTGCTGGTA[C/T]AGAATTCTAGGTTGG | 93664 |
rs183330367 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122741620 | TCAAAAAGCTTAAAC[A/C]AAGATCCTATTCAAC | 93664 |
rs183334346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122339383 | TAATGGTCACCCTTA[C/T]CCATGTTTTGTTGAT | 93664 |
rs183336897 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122468045 | GAAACACTCAGAGTG[C/T]TATTCAGAGATGTAT | 93664 |
rs183345168 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122562485 | GAGCATCTAGAAAGG[A/G]ACAGAACCCTGCTGA | 93664 |
rs183351737 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122634822 | TTAACACTGCTTTAG[A/C/T]GGCATCCCAAAGATT | 93664 |
rs183356561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122782542 | TTTGAACCAGGGATG[C/T]TGAGGCTGCAGTGAG | 93664 |
rs183363731 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122657363 | AGTCATTGGTAGCTT[C/G]ATGGGGATGGCATTG | 93664 |
rs183369956 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122599805 | ATACATACATATAGG[A/T]TACAGTATATACTAT | 93664 |
rs183370985 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122844009 | AGACAGGATCATAGA[C/T]GAGTTAGTTAGGAAT | 93664 |
rs183380917 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122482035 | CTCTGTCTAAAAAAA[A/T]TCTGTATTATTCAGC | 93664 |
rs183387774 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122446377 | TGCTCTTAAATTACC[G/T]GGAAACAGTTTGGCC | 93664 |
rs183395651 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122381512 | AAATGTCATCAGAAA[C/G]CTATTGTATATAAAA | 93664 |
rs183398617 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122408632 | GGGTTTTGCTATGTT[A/G]GCCAGGCTGGTCTCC | 93664 |
rs183419135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122341281 | ACACCTTGTTTTCAC[A/G]TGGCTATCACAAAAT | 93664 |
rs183420158 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122766080 | TGCTTCAACTCATGG[C/T]AGGGAAACGGAAGGG | 93664 |
rs183429025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122808461 | GGTATAACATTAATA[C/T]ACAAGATAACAGTTT | 93664 |
rs183430959 | snp | A/C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122785511 | CAGGTGAATTTTGAA[A/C/T]TAGAGCCCTAAAGGG | 93664 |
rs183433101 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122773470 | AAACTTTAAAGATAC[C/T]TTCGGAAAAGATAGA | 93664 |
rs183436962 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122824147 | GTTGAAAAAAATATA[A/G]ATAATACAGTAAACT | 93664 |
rs183437331 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122482405 | ACATTACATAACGCA[C/T]AGGAAAAGTTCCTTA | 93664 |
rs183440060 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | CADPS2 | GRCh38.p7 | 7:122318788 | GCTAGTCTAGGTACC[C/T]AACGACCACTTATTA | 93664 |
rs183441967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122812928 | ACTGAAAACACATCG[A/G]ATGTTTTTAGTTCAT | 93664 |
rs183442376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122520039 | TAAAAGAGTCAACTA[C/T]TAATAAGGTAGCTGG | 93664 |
rs183460688 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122619928 | CAGAAGAAAGACTCA[C/T]AGTTCTAATCTGACA | 93664 |
rs183460849 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122578428 | GCAAGGAGGTTATAA[C/G]AGAAGATGAATTTGG | 93664 |
rs183469172 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122592962 | CTGCACGTTGTACAC[A/G]TGTACCCTAGAACTT | 93664 |
rs183492203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122553976 | CAAAGAACCTTGGCA[A/G]AGATGAAGGCTGACT | 93664 |
rs183494381 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122819449 | CGGACGCCAAGCTTC[A/G]GGTAACTCTCACAAT | 93664 |
rs183495314 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122649067 | TTGCTTATACCCCAA[C/T]AGTGTTCTCTACCAC | 93664 |
rs183504970 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122851996 | ACCCCTATATACAAA[C/T]CAGGAAACTGAGGCA | 93664 |
rs183506728 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122616860 | AATGAAACCAGAAGC[A/T]GAGATAAATCAAATA | 93664 |
rs183515595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122872884 | CCAGAGGAATGTCCA[C/T]GGACTCACAACCCAA | 93664 |
rs183531792 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122380799 | GCATGTCTGTCTCAC[G/T]TAAAGCCTTTATTGA | 93664 |
rs183537216 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122478566 | TTAAGAAGTTATAGA[C/G]GCTTTATGTAAGTCA | 93664 |
rs183540126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122516972 | ATAAGTATTGACACA[A/G]TCATGTAACCACCAC | 93664 |
rs183543074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122699234 | CATACTGTGAATTTA[C/T]TGGCTTAAATGCTGT | 93664 |
rs183560673 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122684136 | GTTTTTGTTTAGAAG[A/T]TTGGTGATATTTTTG | 93664 |
rs183571907 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122683058 | TGGTTCTTGTCTGGC[A/G]TCCAGGAAGAATCAG | 93664 |
rs183574419 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122739230 | ATGGCAATGGAAATG[A/T]ATGCAAAGAATGACA | 93664 |
rs183580017 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122654647 | GCTCATTGACAATGC[A/G]CTTAGTAACCCAAGG | 93664 |
rs183584095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122725190 | TGTCTAAGTCATAAT[A/G]TAAGTAAATGCTATA | 93664 |
rs183585957 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122726470 | GTGAAGCCAGCCCCC[A/C]CTGTGACTGTGCTAA | 93664 |
rs183597697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122596239 | CTCAAGAACATTTAA[A/G]CTCATTTTGTTAGAA | 93664 |
rs183600745 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122761068 | TAGTCTTGTTGAAAA[A/C]TTATCATGAAACATA | 93664 |
rs183607394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122578979 | TATTTAATAACTGCC[C/T]CTATGGAAGGCTTTA | 93664 |
rs183607889 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122804700 | AATGCATCATAAAGG[C/G]TCAGTGTTCCTATAT | 93664 |
rs183610507 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122532146 | TTTGGGAAATTCTAT[A/C]AATTGGCTGATTTTT | 93664 |
rs183616527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122551552 | AAGATCTATTTGACG[C/T]CCACATTATTAAAAC | 93664 |
rs183616674 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122596691 | GACATAAAAGGCACA[A/C]ATTACATATTCAAGA | 93664 |
rs183632603 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122556877 | TTAGCTCTGATAATA[A/T]CACTTCTTCCTATTG | 93664 |
rs183633923 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122476561 | GCTAAGGTAACAAGT[A/C]TTTCCAAATGACACA | 93664 |
rs183637262 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122513730 | CAGCTGCAGAGCCAA[A/G]AATCCAGGGTGAAGG | 93664 |
rs183646609 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122559396 | CAGTCCGTTTCCACC[A/G]CTCTCCACGAAAAGA | 93664 |
rs183649466 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122494002 | GTTATTTAATCAAAC[G/T]CTAATTTAAATGTGG | 93664 |
rs183659608 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122779282 | GTTCCCACACTTTAG[C/G]TGGGACAGCTCTACT | 93664 |
rs183660489 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122459807 | GGACCACTTGGTCAG[C/G]TCATGGGACACAATG | 93664 |
rs183670397 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122423636 | CCAAATGATATTATG[A/G]TTCCACAAGTGTTGG | 93664 |
rs183670940 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122758962 | AAATTTTTACTTAGC[A/G]CAAACCAAAAATAGC | 93664 |
rs183672899 | snp | A/G | 0.00173179 | 0.0293751 | intron-variant | CADPS2 | GRCh38.p7 | 7:122438504 | TGAGGGGCAGGGTTG[A/G]GGATAGACAGATGGA | 93664 |
rs183673364 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122800528 | AGTAGTAGATGTAGG[C/T]TGGGGGCTGAGAATT | 93664 |
rs183682641 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | CADPS2 | GRCh38.p7 | 7:122837086 | AAACTGTCTCTCAGA[A/C]CACAGTGCAATCAAA | 93664 |
rs183701478 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122500672 | CATAGTTATAAGAAA[C/G/T]CCATCAAAATACCAA | 93664 |
rs183703164 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122734270 | TGATGTCTGAGATTG[C/T]TAATAGATTTTGAAG | 93664 |
rs183711269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122688559 | TCTCTTAGAGTGTCC[A/G]CTCTGTCTCAGCTGT | 93664 |
rs183719061 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122601012 | AGAAACACAATTTTT[A/T]AAATGTGGATAATGA | 93664 |
rs183727388 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | CADPS2 | GRCh38.p7 | 7:122836932 | ACCAAGCGGACCTAA[C/T]AGACATCTACAGAAC | 93664 |
rs183728202 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122618494 | CTTGGTAAGGGAATA[C/G]GGTATGGTGGGAGAA | 93664 |
rs183750195 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122586594 | ATTGCAGCTTTGCAA[C/G]ATGTTATGTTATCTG | 93664 |
rs183752394 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122772129 | CAGTGGGAATGTTAA[C/T]GTAATACTGCTTAGA | 93664 |
rs183758914 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122398723 | AGAACAGCATTATGT[A/G]AAAGGAAAACACTCT | 93664 |
rs183760577 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122866317 | ATTGCTATAGTCTCC[A/G]AATTGGTCTTTCTTC | 93664 |
rs183763513 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122327603 | TGCATCTTTATGTTC[C/T]TGAAAATCCTTATAT | 93664 |
rs183764735 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122361065 | TATGCATACAAACTA[A/G]TAGCAGGACAAACAA | 93664 |
rs183770961 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122639199 | GGGGATAAATTAGTT[C/G]GTTAACGTTCTTTTT | 93664 |
rs183778215 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122444269 | ATAATGTTGGTATGA[G/T]CAATCATATAAAAGT | 93664 |
rs183781360 | snp | A/C/G | 0.00239393 | 0.0345281 | intron-variant | CADPS2 | GRCh38.p7 | 7:122841616 | TCCTCAAGCTTTGCC[A/C/G]CAAGAGTAGGAGAAA | 93664 |
rs183783007 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122464844 | GGAGCAGAAAAAAGG[A/T]CATTAATTTAAAAAA | 93664 |
rs183792708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122862277 | TGTCCTCAAATTCAC[C/T]GTCTATTCTCTGCTC | 93664 |
rs183798315 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122884767 | GATACTTATACACCT[A/T]TGAAACCACCAATAG | 93664 |
rs183798439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122669564 | GAAGGAAATGGGCTT[C/T]CACATGAGGGAGGAA | 93664 |
rs183802495 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122510628 | ATTCACATTATCAAC[A/C]GAGCATCATTCTGCC | 93664 |
rs183815324 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122548006 | GAGTGTGATGGTAAC[G/T]ACAAAATAAAAGTCA | 93664 |
rs183817257 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122474700 | AAGCCTAAGTAAAAA[C/T]AACAGCAAAAAATCT | 93664 |
rs183823506 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122611788 | GGACAATATCTCTTA[C/T]GAATATAGAGGCCAA | 93664 |
rs183825320 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122876601 | CTCCTGGGCTTAAGT[A/G]ATCCTTCTACCCCAG | 93664 |
rs183836942 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122801017 | AAAAAAAGAAAATTC[A/T]AGTGAACTTCTTACC | 93664 |
rs183842125 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122759124 | TTTGCCATTTTCCCT[C/G]TAAGTGGAGAATCAC | 93664 |
rs183843419 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122780780 | CCCAAAGTGTTAGCC[A/G]TTCTTTTAAGGGCTG | 93664 |
rs183845105 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122436891 | ATATCTTTTCTGTAT[A/C]CGTGGACAAGTTAAT | 93664 |
rs183846649 | snp | C/T | 0.250168 | 0.25 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539829 | TTTCTGTCTCTCTCT[C/T]TCTTTCTTTAGTAAA | 93664 |
rs183847404 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122409848 | ATCAAGGTCTCCACC[A/G]GGGAGGAGAAAACCT | 93664 |
rs183854524 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122577250 | ATTTCTTCACAGCAG[C/T]GTGAGAATGGGCTAA | 93664 |
rs183894575 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122819735 | CTATTCCTGGACTAC[A/C]GCTATATCTCATCGC | 93664 |
rs183899852 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122506014 | GGTAATCTGGAGAAA[C/T]TGTACTCAGACCTGT | 93664 |
rs183900805 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122856200 | GTTCTTGTGAAGTAA[G/T]CCCAGTGGTTTAAGT | 93664 |
rs183908459 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122675964 | TGCACGTTCTGTACA[C/T]GCATCCCAGAACCCA | 93664 |
rs183908930 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122721520 | TGAATAGACCAATAA[C/G]AGGCTCTGAAATTGA | 93664 |
rs183911138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122473059 | ATGCTTTTAAATCAA[A/G]TTTAGCCTAAAGCTG | 93664 |
rs183926041 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122673254 | CCCCAGCCGGTTGCC[A/G]CAGCTGGCTCTGGCA | 93664 |
rs183929975 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122535760 | GTTGTAGATTGATGG[A/G]ATGATATACTGAGCC | 93664 |
rs183935448 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122453367 | TAGAATCAATTCCCA[C/T]TGAGCGAATGTTAAT | 93664 |
rs183935792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122487716 | AATGAAAGGATATTT[C/T]ATAGTCATGGCTGGG | 93664 |
rs183941316 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122794158 | GCCACTCTAGGTAGA[C/T]TGGGGAAGTTCTCAT | 93664 |
rs183942698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817883 | GACCTCTTATCTCTG[C/T]GCCCCAATCCCTTAT | 93664 |
rs183942971 | snp | A/G | 0.0018478 | 0.0303395 | intron-variant | CADPS2 | GRCh38.p7 | 7:122386969 | CCTTGTGGAAAGGGC[A/G]TTTCCCATGCCAAGG | 93664 |
rs183944876 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554134 | AATGTATATAGCCTC[A/G]TTGGGTTACATCTAC | 93664 |
rs183945142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122752940 | TGTAGAAAGGAAGGA[A/G]ACAAGAAGAAGATGG | 93664 |
rs183947620 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122434739 | ATTCAGCGACTCAGC[A/G]AACTCTTTCCTAGCA | 93664 |
rs183954822 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122368945 | CCCAGCTGGTAACAT[A/C]AGAAAATGGGACTAG | 93664 |
rs183955240 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122396106 | TGAGCTACTGCGCCT[A/G]GCTAGAACTATTTTT | 93664 |
rs183955340 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122566952 | ATAATATGTCCATGG[C/G]CTTACCCTCAAAAGG | 93664 |
rs183957204 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122478752 | GTAGGCACTGACCGC[C/T]ACCTGCCCCTTAAGT | 93664 |
rs183960775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122416658 | AGTCACCTAAAACAA[C/T]TCTGACAGCTAGCAA | 93664 |
rs183964491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122517149 | TGGAATTATTCAGTA[C/T]GTAGCCTTTCTGTCT | 93664 |
rs183966386 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122435844 | AAAAAACAAATTTCT[A/G]GCTTAATAGTAAAAT | 93664 |
rs183967005 | snp | C/G | 0.0271762 | 0.113356 | intron-variant | CADPS2 | GRCh38.p7 | 7:122836168 | CCCAGAATTTCATAT[C/G]CAGCCAAACTAAGCT | 93664 |
rs183970018 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122646371 | AATGCAAAGTACAAT[A/G]TGACAGGCTTTTGGG | 93664 |
rs183971698 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122496838 | TATTCACGTCCATTA[G/T]GTCAAATTTACTAAT | 93664 |
rs183972757 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122347092 | GCCTTGCATCATTTC[A/G]TATTCACAGAAAGCA | 93664 |
rs183973064 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122852819 | AACAGAGAAGCAATC[C/T]GACTTCTGTTATAAC | 93664 |
rs183975742 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122874007 | CCCACTTTTTGATGG[G/T]TTTTTTTTTTCTTGT | 93664 |
rs183975761 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122323466 | CACTAGTGAGAATAC[G/T]TAAGATCTACTCTCT | 93664 |
rs183978464 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122612353 | TCAGTAAGGTTGATT[G/T]ATGCATATAAAATCT | 93664 |
rs183984338 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | CADPS2, LOC105375481 | GRCh38.p7 | 7:122530022 | ATATTTTGGAATTAG[A/T]GCTATTTGACTCACT | 93664 |
rs183993867 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122835696 | TCAGTGATGGAAGAT[C/G]AAATAAATGAAATGA | 93664 |
rs183999090 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122859575 | AATGAAAAACATAAG[A/C]AAAATAGAGAATATT | 93664 |
rs184016884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122455926 | CAGGCTGGTCTCGAA[C/T]TCCTGGCCTCAGGTG | 93664 |
rs184020930 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122692104 | TTCCACCTGACTGCA[A/G]CAGGCAATCTGTGAA | 93664 |
rs184022746 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122433788 | AGTTGACCAGTGGTA[C/T]GGATTGCTAAGTCAC | 93664 |
rs184022913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122489789 | CAAAAATCACAATAA[A/G]CTAAATTAAATTTTC | 93664 |
rs184022934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122429365 | TAGCTCAAGCAATGA[A/G]TTTTTACAAATCATA | 93664 |
rs184024099 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122676569 | ATGCTGTTAGCCCCA[A/G]TTAAATATCCACTTC | 93664 |
rs184025453 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122394700 | CAATAGACTGAGGGA[C/G]GGGGAGGGGCAGCCC | 93664 |
rs184029481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122390179 | ACTCCCGTAGCACTT[C/T]ACTCACTTAAATCTC | 93664 |
rs184031880 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122640659 | ATTGTTGGCTGGGCG[C/T]GGTGGCTCACGCCTC | 93664 |
rs184040659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122662621 | CCTCACTATCTGCCC[A/G]CCTCAGCCTCCCAAA | 93664 |
rs184041960 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122719816 | AATCATGACTGAAAA[A/T]AAGGAAAAAATATCA | 93664 |
rs184044807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122623860 | GTTCTGATATACTAA[C/T]GCTTTGCTTTCAAAT | 93664 |
rs184050100 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122731249 | AGTCACAAATTTTTT[G/T]TTTTTTTAAGAAGCT | 93664 |
rs184053025 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122355413 | GGTGAAACCCCATCT[C/G]TATTAAAAATACAAA | 93664 |
rs184063213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122758407 | TTATAAACATCGCGT[A/G]TGTATTATAATGACC | 93664 |
rs184065081 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122704831 | TGCTTCTGCAGACAT[A/T]TTTTGATTGTCACAA | 93664 |
rs184070927 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122724767 | TGTGTTTAAATTCTA[C/T]TTCCTCTGTGCTGAA | 93664 |
rs184085264 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122820101 | GCCTATCCACCCTGT[A/G]GTGCCAAACCCATAT | 93664 |
rs184085578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122776249 | CATGAGATCTGATGG[C/T]TTTATAAAGGGCAGA | 93664 |
rs184090314 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122711011 | AAGACATATCTGGAG[C/G]TTTTATAATCTATGC | 93664 |
rs184093835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122390601 | TACATGGCAATCTTC[A/G]TAGAGAATATGGTTA | 93664 |
rs184093926 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122805141 | CCTGATAAATGCTGA[A/C]AGCATTTTCAATCAT | 93664 |
rs184095317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122754459 | TAATTTTGAAACTTT[C/T]GTTTTCATGAAATGT | 93664 |
rs184095445 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122837507 | TGGTTTTTTGAAGAG[A/T]TCAACAAAATTGATA | 93664 |
rs184098531 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122799647 | TAGCTATCTAGAATG[C/T]AATTAACCTAAATAA | 93664 |
rs184099651 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122373424 | TATGTGTGCTAACAT[G/T]TAAGAATCATTGCCT | 93664 |
rs184101198 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122352445 | GTGACGACTCAGGGT[A/G]CTAGAATTCCAGTGT | 93664 |
rs184105456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122856491 | AGTTCCCTACACTAC[C/T]AAAATGTCACCAAAC | 93664 |
rs184110672 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122330812 | CAGGGAAGAACACAA[A/C]TGCAGACCCCGTGAG | 93664 |
rs184124701 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122660984 | AAAATAAAGACTTAT[G/T]TTAAAAGTAAACAGA | 93664 |
rs184125271 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122695751 | GTCCACATTAACAAA[A/G]GTTATATCATAGAAG | 93664 |
rs184127350 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122570897 | GTGAGGTCGGGGGAG[C/T]GGGGAGGGATAGCAT | 93664 |
rs184127901 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122596555 | TGTAAACAAATACTA[C/T]AGCAGTGAGAAAAGC | 93664 |
rs184129634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122707643 | CAACTATGTATGTTT[C/T]TTTTGCAAGAAATTA | 93664 |
rs184133916 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122681343 | GAAGGAACAATGGTC[A/G]TGCCAAAAAGGGCCG | 93664 |
rs184146654 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122735648 | AAGAACTCCCTCATC[C/T]CCCTGCTGATCCAAT | 93664 |
rs184147085 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122540631 | TTAAAACGGCAAGGC[A/T]TATTATTAAGGTCCC | 93664 |
rs184157876 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122450878 | TGCTAGGTGCTGTGA[C/T]CTGTGTTCTCAGAGA | 93664 |
rs184159350 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122880636 | GAAGTTTTAACACTA[C/T]ACCCCCTGAGACTGA | 93664 |
rs184162205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122869628 | CACTAAGGAGCAACA[C/T]AAAAATATCAAACTC | 93664 |
rs184164234 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122783110 | GGTCCCAGCTACTCG[C/G]GAGGCTGAGGCAGGA | 93664 |
rs184164829 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122468882 | AATTTCCCTCAACCC[C/T]ATATTTCTTCCTTTC | 93664 |
rs184166190 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122415068 | TTAAGTCTCAGAATG[A/G]GCAGTTTGCTTGGTG | 93664 |
rs184166963 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122722899 | CAACAGTCTGATCTT[A/T]GACAAACCTGACAAA | 93664 |
rs184168180 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | CADPS2 | GRCh38.p7 | 7:122502049 | TTACCTCTTAATTTC[C/T]GGCAAAGTTATTATT | 93664 |
rs184175030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122545936 | TATTAATATTGATAC[A/G]TAAAATAACCAGAGG | 93664 |
rs184175338 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122563153 | ATTTCATCCTTCTTA[A/G]ATAGAGCAATATACT | 93664 |
rs184185594 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122644497 | GAGCTTTATATATTT[C/T]ACCTTACCCTAATGA | 93664 |
rs184186160 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122586157 | AAAAGAGGGAGGATA[C/T]AAAACTGAACGTGCA | 93664 |
rs184188009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122376025 | AATGCAAATCAAAAT[C/T]ACAGTGAGATATTAG | 93664 |
rs184189477 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122506933 | GAGAATGATTTGCAT[A/C]TATTTATTTACTTAA | 93664 |
rs184195938 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122401999 | TAATCATGGCTAACT[C/G]TAAGGAAAGGCACAC | 93664 |
rs184197629 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122487802 | GAGGAGTGAATAGAA[A/G]TAAAATGTGCAGTAG | 93664 |
rs184199818 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122738462 | TGGAGATAAAACAAC[A/G]AATTCCAAAATACAT | 93664 |
rs184203033 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122626936 | TGAAGTACTAAAGTC[A/G]ACATGTCTCTTGAAA | 93664 |
rs184204877 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | CADPS2 | GRCh38.p7 | 7:122334631 | TGCAGGTGCTAGAAC[C/T]GGATACAAACTTTGT | 93664 |
rs184205970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122363144 | ACTCAACTTGATGTA[A/G]TTTGCAAGGACCCAG | 93664 |
rs184208304 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122527999 | TTTGTAAAACAAGAA[C/T]AGCAATATTAGCTCC | 93664 |
rs184209299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122430044 | GCCACAGTACAACTT[C/T]TCCTCTCAAAGACAG | 93664 |
rs184224167 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122574328 | GCATACACCTATGGC[C/T]TCAGATACTCTGGAA | 93664 |
rs184224681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122874738 | TGCCACACATCTACA[A/G]CCATCTGATCTTTGA | 93664 |
rs184229923 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122778792 | TGAAATGAGTTAAGA[C/T]TCTGGGGACTGTTGG | 93664 |
rs184235282 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122593973 | TCCTTTAAAACATAA[C/T]TTACAGTCTATAATA | 93664 |
rs184239314 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817594 | TCAGACCACCCAGGG[A/G]TGCCTGCCTTGGTCC | 93664 |
rs184240842 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122670252 | TCTTCCACCAAAATC[G/T]TCACCATGGCCTCTG | 93664 |
rs184242410 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122608731 | AAACAGCACTATGGG[A/G]TGAAGGAGAGACAGA | 93664 |
rs184246828 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122838800 | AAACAAATGGAAGAA[A/C]ATTCCATGCTCATGG | 93664 |
rs184251922 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122536921 | AGATTAAGGGAAGCT[A/G]ATATCTGAAAATACC | 93664 |
rs184262569 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122692495 | CCTGGTGCTTCAGTA[A/C/T]CTTCTCCACACTCAT | 93664 |
rs184264736 | snp | A/C | 0.00113986 | 0.023846 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554706 | TGTATGGAAAAAAAA[A/C]CCCACATTTAAACGC | 93664 |
rs184282404 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | CADPS2 | GRCh38.p7 | 7:122521481 | TTTTTGCGGGGGGGT[G/T]AGGTGGGGGGGCTTG | 93664 |
rs184310958 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122600852 | AGAACACGAGAATGA[A/G]GCAACCTGAAACACT | 93664 |
rs184326383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122483313 | GCAGCACATTTCTCA[C/T]TGGAAAAACAAATGC | 93664 |
rs184334775 | snp | A/G/T | 0.00159649 | 0.0282165 | intron-variant | CADPS2 | GRCh38.p7 | 7:122448909 | TTCTGTAGGCTTAAC[A/G/T]GCTAAGGTGTGAGAT | 93664 |
rs184339135 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122430522 | CTTCAGTGTTATCTC[A/T]GCATGCCAGAATTAC | 93664 |
rs184339678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122605986 | CCTATTTAAATGTCC[C/T]CAAACCACACAGTGA | 93664 |
rs184342864 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122640070 | GTACCCCGATCATTC[A/G]TGAGTAATGCCGTGT | 93664 |
rs184345815 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122410470 | TTTTTGTAGTAAATA[C/T]AGTTTACAACAGTGG | 93664 |
rs184347263 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122878154 | CCAGCTAGCTACTCG[C/G]GGGGCTGAGACAGGA | 93664 |
rs184347949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122382339 | ATATTTGTGTGTGCA[C/T]GCATTTAAAATAAGG | 93664 |
rs184354459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122848798 | GACACCTAAGTAACC[A/G]GCAGCTTCAAGCAAC | 93664 |
rs184357254 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122412232 | TCCAGATATCAACAA[G/T]GTGTAATTGAGGTCA | 93664 |
rs184364031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122427045 | TTCTAGCAAGAGCTG[C/T]TCAGAGTGTTACAGA | 93664 |
rs184365163 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | CADPS2 | GRCh38.p7 | 7:122391265 | TAAATTTCCCCAGAA[A/T]GGTGAAAGCACAATC | 93664 |
rs184367973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122373594 | CCTGCTGAAGTCAAT[C/T]GGTAAATAGTGGAAA | 93664 |
rs184368029 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122871033 | GCAAATATTAATCAC[A/T]TTATTGATGAAGATA | 93664 |
rs184380378 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122386795 | CAGCTGTTAAAAGCT[A/G]TATCTAAAATTCATG | 93664 |
rs184396203 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | CADPS2 | GRCh38.p7 | 7:122705476 | ATTATATATTATATA[C/T]ATTTATATTATATAT | 93664 |
rs184399266 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122346267 | CAGCTAGCCAGGAGG[G/T]TGAGGCAGGAGAATT | 93664 |
rs184402008 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122751792 | TTAACAAGGCTGCTA[C/T]GCAGTGAAATGCTGT | 93664 |
rs184412522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122720560 | TATGTATATATGCAT[A/G]TGTCTGTATATACAT | 93664 |
rs184423448 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122790185 | GAGGATTGCTTGAAG[A/G]CAGGAGTTTGAGGCC | 93664 |
rs184429600 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122426389 | CAATCACTGTGAATG[C/T]GTGTGCATGCATTGA | 93664 |
rs184434906 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817788 | AATTACCCCAACCTC[A/G]TATCTCTGCGCCCCA | 93664 |
rs184443688 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122852478 | AAGCTTACAGATGGG[C/T]AGAAGTGTATGTGGG | 93664 |
rs184448840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122626258 | TGTTAATGAGGACAG[A/G]GGTAGAATCCAGGAG | 93664 |
rs184453914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122655693 | ATCTCCAAGGTATGC[C/T]TGCATAGCATTCAGG | 93664 |
rs184454273 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122674127 | GCCGCTCCAAGTGTG[C/G]GGCCCACTGAGCCCA | 93664 |
rs184456360 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122659544 | TATCTAGAATACCAG[A/G]AAAAGAATAAAGAGG | 93664 |
rs184457237 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122589991 | ATCACGTATACAGAA[C/T]TTATCCGTCACCAAA | 93664 |
rs184462801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122716171 | TTTTTTAAAAAACTG[A/G]TCTGAAGTAATGGAA | 93664 |
rs184472104 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122727768 | GATATTGTATACAAC[A/C]ATAGGAATCTCAGAC | 93664 |
rs184474405 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, utr-variant-5-prime | CADPS2, RNF148 | GRCh38.p7 | 7:122702829 | ATAAAGAAGATAGCT[C/T]GTTGGCGGCAGATTA | 93664 |
rs184475684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122623699 | TCTTTGGTCTGGTTT[C/T]AACACCTAACTTGTT | 93664 |
rs184478435 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122873608 | CAAGTCTTTGCTATT[A/G]TAAATAGTGCTACAG | 93664 |
rs184482051 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122734660 | ATATACTTCTAAAAA[A/C]ATGAAAGGCATTTTG | 93664 |
rs184482849 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122593644 | TTTACTAAATAATAT[C/G]TACCTGAAAAAATTG | 93664 |
rs184485479 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122657612 | TTGGCTCTCTGTTTG[G/T]CTGTTATTGGTGTAT | 93664 |
rs184492043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122469228 | AGTCTCAAACACATA[C/T]ATTTTGGGGGCACAT | 93664 |
rs184493615 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant, downstream-variant-500B | CADPS2, LOC105375481 | GRCh38.p7 | 7:122564124 | TACCACCTTAAACTG[G/T]GAAGGTGAGCTCTTG | 93664 |
rs184500772 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122492210 | AATAAATTAATTAAT[A/T]AATTAAATTAAATTA | 93664 |
rs184503716 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122449261 | CACTGATTTTCATTG[A/G]AAGATACATAAAATA | 93664 |
rs184508994 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122488111 | AGGTAAGAAACAAAT[G/T]TATAAAAACTTGGTT | 93664 |
rs184509540 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122483417 | ACTTTTTTTCGTATA[C/T]AAAGAAGCTAAAAGT | 93664 |
rs184512433 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122404998 | CAGGTGTGTGGTGGC[A/G]GGCGCCTGTGGAGGC | 93664 |
rs184515019 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122645154 | ACCGTGGGACTTCTA[C/T]AACCTAGAGAATATG | 93664 |
rs184517496 | snp | A/G | | | intron-variant, upstream-variant-2KB | CADPS2, LOC105375481 | GRCh38.p7 | 7:122528256 | TGTCCCATTTAAGGA[A/G]AAAAGCTTTCCAAGA | 93664 |
rs184522446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122368574 | GGCCCCAGGCCTCCT[C/T]TCCCTTCTTAATCAG | 93664 |
rs184523288 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122628333 | TTCTTGAATGCTGGA[A/G]GAGTTCATTATCTTG | 93664 |
rs184525567 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122454317 | AAGGCTGCTGAGGCT[C/T]AGGGCAGTTAGGTTA | 93664 |
rs184539950 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122322573 | CAAAAGAAGCAGGTG[A/C]TTTATGTTAACTGCA | 93664 |
rs184544190 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122733173 | ATATATATCTAGCAT[C/T]TTCAAGGAAACACAA | 93664 |
rs184553986 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122835856 | TTGGAAAACACTCTG[A/C]AGGATATTATCCGGG | 93664 |
rs184560609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122740059 | CCATTAGAAAGAACA[A/G]AATCCAGAACACAGA | 93664 |
rs184563163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122712450 | GACCCTACTATGTGC[A/G]TAGTACTTAATAGTA | 93664 |
rs184564863 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122768977 | AAAAAAGAAAGAAAC[G/T]GTCACAGCTGTCAGA | 93664 |
rs184569920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122767372 | AAGTGATAGAGCTGG[A/G]ATTCAAAACCCAGGT | 93664 |
rs184570782 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122810593 | AGGCTATGTAATAAT[A/G]TAATAATGTTTAAGA | 93664 |
rs184573758 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122667533 | TTCAGGGATTCTGCT[A/C]AGTGTTGGGGGCACA | 93664 |
rs184579000 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122809538 | TGCGCTGAGATCGTG[C/T]CATTGCACTCCAGCC | 93664 |
rs184580154 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122651443 | GCAACTGCCTATTTA[C/T]TGATTTCTTTAAACT | 93664 |
rs184587918 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122636436 | GCCCCCATCCTCTTC[C/T]GGCTCGTAAGGTTTC | 93664 |
rs184595849 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122341657 | GAAACTTGAGAAATA[C/T]GATTTCAAAGTTTGA | 93664 |
rs184603560 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122656845 | ATTTTGGCTTTTGAC[A/G]CCATTGCTTCTGGTG | 93664 |
rs184606502 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122695442 | TGAATAAATTTGATA[C/T]AGTAGTGCTATTTCC | 93664 |
rs184606638 | snp | C/G/T | 0.00716713 | 0.0594884 | intron-variant | CADPS2 | GRCh38.p7 | 7:122680662 | GAGGTTGCAGTGGGT[C/G/T]GGGATAATGCCACTG | 93664 |
rs184606967 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122546627 | GCTGTACTTTTGCTG[A/C]TATTGCCCTTCACTA | 93664 |
rs184610928 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122573854 | AATAATATTTGATTT[C/G]TGAAAAATCTCTGCA | 93664 |
rs184618555 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122642921 | TTTTTGAGTGAATTG[C/T]ACTCTTTTGTTTTCT | 93664 |
rs184622620 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122608364 | AACTAATATGCTTTT[A/T]AAAAGCACGGTTAGA | 93664 |
rs184625146 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122483772 | TATACATGAAGATAT[A/G]TAATAAATTTAAAGG | 93664 |
rs184630244 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122684493 | TACAATTAACATTTT[A/G]TTCTATTTGTTCTTT | 93664 |
rs184646666 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122479281 | ATGTTTAGGAGTTCA[C/G]CTGTAGCTGCATTTA | 93664 |
rs184651248 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122507752 | AGAACAGCTAGGATG[C/T]TATTGTAGGAATCCA | 93664 |
rs184652069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122606426 | ATCCAGGTAGCCTCA[C/T]AGTTTGAAAAACATC | 93664 |
rs184656337 | snp | A/G/T | 0.0103333 | 0.0711729 | intron-variant | CADPS2 | GRCh38.p7 | 7:122647748 | TTTCAAAATGCTTTA[A/G/T]AAAAAGCTTTATATG | 93664 |
rs184663198 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122544554 | ACGCTGGCTAGCTGG[C/T]TTTGTTCATTTCATC | 93664 |
rs184673837 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122473548 | ATATTTGAAACAGTT[A/C]TGGTCCCAAGCATTT | 93664 |
rs184677289 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122444845 | ATGAATTATGATTAT[A/G]TTTTATTTAAGAATC | 93664 |
rs184681812 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122725850 | TCCATACTGAAACAG[A/G]AAGTACTTAAGAGCA | 93664 |
rs184688782 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122405934 | TGTTGGTGCTATTAT[C/T]TTCCTTCTTTTATAG | 93664 |
rs184703906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122749744 | AACTTCAATACATCA[C/T]TGTTAACAAATTTAC | 93664 |
rs184710453 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122669991 | CCCAACATACAACTT[A/G]TCCCTGAACCCTGCT | 93664 |
rs184717586 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122787593 | TCCATATCCATCTCC[A/G]CCAATAGACAGCTGG | 93664 |
rs184724193 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122655471 | TTGCTGAAGGCTCAA[A/G]TGCTTGGTAGCATTT | 93664 |
rs184729850 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122639785 | AAACTGGAGATGTGG[G/T]CCCTTGAGCGCTCAT | 93664 |
rs184733668 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122597522 | CCCTGTGTCAGTAGA[A/G]AATAATTATAGAATA | 93664 |
rs184748327 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122377613 | CAAAGTTAACTTTAT[C/T]TCACTGTAGTGCGTT | 93664 |
rs184749624 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122683868 | ATCCCAAAGACATGT[A/G]TATGAGGTTCACTGT | 93664 |
rs184758558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122337117 | ATAATAATTTAGCCT[C/T]CTGGGAGGGCCCCAA | 93664 |
rs184760807 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122763525 | ATACTGTCAGTAATG[A/C]CATCATATCCATCGT | 93664 |
rs184761486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122605442 | TGAAACATCATTATG[C/T]AGTGTATGACTATTT | 93664 |
rs184762371 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122579775 | ACAAATGCACAAATA[C/T]GTAAGCACATGACTG | 93664 |
rs184762904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122745447 | TCTTTCCGATTACCA[C/T]ATTATTCCGTTTCCC | 93664 |
rs184765317 | snp | A/G | | | intron-variant, upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122622039 | GATATTTTAGCGTAT[A/G]GATGAACCTTAGCCA | 93664 |
rs184770179 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122503275 | TCCTGACCTTGTGAT[C/T]TGCTCGCCTCGGCCT | 93664 |
rs184776593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122699496 | TGTGAGGCAAAAGTG[A/G]TGAGCTTAGTGACAT | 93664 |
rs184783549 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122541894 | ATATATATTCATATA[C/T]ATTTATATATTCATA | 93664 |
rs184788941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122522818 | TTACATGTGAGAACA[C/T]GTGCCATCTGTCTTT | 93664 |
rs184790997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122671191 | ATCTCTTTTCCTCAC[C/T]GGACAGTAAGTTCCA | 93664 |
rs184801351 | snp | C/G/T | 0.000198733 | 0.00996641 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122702270 | AGTGCAAAATTTCCA[C/G/T]GCCTTTCAGGTTGCT | 93664 |
rs184804578 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122652264 | CTACATATATATATA[C/T]GCTCTGCATGATTAT | 93664 |
rs184806533 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122465403 | GGGGTCCCCAATACC[C/T]GGGCTGTGGACTGGT | 93664 |
rs184808051 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122497546 | ATTACCCATTCCCAT[C/G]TGTTAACTCAGTCCT | 93664 |
rs184811060 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122525526 | CAGTAAGATACGCTT[A/G]CTGTTAATCCAGCTC | 93664 |
rs184814075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122673768 | TAGTGGATCCCACAC[C/T]AGGGCTGCAGGCAGA | 93664 |
rs184838080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122427335 | GGGCACGCTATGTTT[C/T]ATAAGAAAGTTAAAA | 93664 |
rs184862299 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122437908 | GTTCTATGAGTTTAT[G/T]TCAGCCCTCAATAAT | 93664 |
rs184863601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122518092 | TATGCTCCACTAGGC[A/G]ATAGATTTTGTTCAT | 93664 |
rs184869218 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122401653 | CTCAATTTGAATACA[A/T]CTCTCTTTCAAAAGT | 93664 |
rs184869321 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122806095 | GATTTCTTGAGGCTT[C/T]TGGATTTTCTTAATG | 93664 |
rs184872753 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122422344 | TCTTCTACGTGGAAC[C/T]CCAAATGTCAGCCAG | 93664 |
rs184872866 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122784370 | AAAACAGCTATCTCC[A/C]TCCATGTACTTTCTA | 93664 |
rs184877601 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122833538 | CCCAGCTTTGTTTTT[G/T]TTTGTTTGTTTGTTT | 93664 |
rs184877795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122357397 | GATCAGCACTTTCCT[C/T]GCTCCTCTTTCAGTG | 93664 |
rs184879207 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | CADPS2 | GRCh38.p7 | 7:122822082 | GGTTTACACTGTTTT[A/T]CCAAGCCATCACAGC | 93664 |
rs184883973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122847148 | CTGGAGTGCAGTGGC[A/G]CAATCTCAGCTCACT | 93664 |
rs184885913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122868453 | CTACATCTCAAGAGG[C/T]TGTCTTCTCTCACCT | 93664 |
rs184890176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122382177 | CTTCTTCTGTGTTTT[C/T]TAATCCTTGCTAAAA | 93664 |
rs184892422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122362823 | TGCATAGGAGATAAT[C/T]TTTTCTTTATGGCTG | 93664 |
rs184896612 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122796568 | TAAGGCTGCACACCT[A/G]CAACTATCAGATCTT | 93664 |
rs184900244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122342588 | TTTGCAGACTAATTG[C/T]TTTATATAAAAATAG | 93664 |
rs184901185 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122478091 | ATGTTACTCTTGAGA[A/G]ACACAGCCATCATCT | 93664 |
rs184903495 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122461601 | TTTTTGTTGTTGTTT[C/T]GTTTTGTTTTTTAAG | 93664 |
rs184904904 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122834032 | GGGTGGAAAAAAAGA[C/T]GGACATACAGAAACC | 93664 |
rs184914157 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122667828 | AAGAAAATAAAAGAA[C/T]AACAGCAATAAAGCA | 93664 |
rs184918861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122688922 | TTTGGTACATAGGCT[C/T]GATATATATACACAC | 93664 |
rs184930466 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122726949 | TAAAGAGCATTTCCC[C/T]GATTAATGAAGGAGT | 93664 |
rs184952160 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122762641 | TTTCTCCCATGCACC[A/T]CTCTCAAGAAAGAGG | 93664 |
rs184985678 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122677360 | AGTGGGTAGAGGGAA[A/C]ACAGCCTATCTAAGG | 93664 |
rs184987802 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122664013 | AACACCCTGATTTTG[G/T]ACTTCCCAAGCCTCC | 93664 |
rs184997241 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122537209 | AGCATGTATACAACT[A/C]TTTATCAAAGAAGTA | 93664 |
rs184998599 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122648254 | ACTCTGTCCTGGGCT[C/T]CTTTTCTCCTTGAGC | 93664 |
rs185011318 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122404676 | CTTGACTTTTTAATG[A/G]TTACTATTCTAACTG | 93664 |
rs185017372 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122815645 | AAAATATATTGCAGC[A/G]AAACGTTAGACATCG | 93664 |
rs185019825 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122789566 | CTAGAGGACACAAAT[A/G]CAAATTTTCCCCCTA | 93664 |
rs185027911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122826600 | CAAAGGAAAAGAACA[C/T]CTCAGCAAGGCAACA | 93664 |
rs185031999 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122810049 | GAGATCTCAGCTATA[A/C]CTTGCAGTAGAGGAC | 93664 |
rs185033138 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122848188 | CTCTGATAAAAGCAA[C/T]GCTCTTACTCTCAAG | 93664 |
rs185033896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122386656 | TATTTCACACTTTTT[C/T]GTGTGTCTTACTTTT | 93664 |
rs185034673 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122553330 | ACTGGTGAGCAGGTA[A/G]ATGGATGCATGAATT | 93664 |
rs185034718 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122597822 | ACTGTGGATTTTTGT[C/T]CCAATTTACTCAGGT | 93664 |
rs185039045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122571888 | ATGAAGTAACAGATG[A/G]GGAGTAGATTAAAGA | 93664 |
rs185041729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122367041 | ACTTTGCATTCTCTC[C/T]CTGCTAAAGGCTCCT | 93664 |
rs185042019 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122346059 | TGCATCATCTCTGGC[G/T]GGCTTATCAATAATA | 93664 |
rs185043622 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122473236 | GTTCAAATAAGGCAA[A/C]TGCTGAACTGTAATC | 93664 |
rs185046918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122614628 | TAAAGCGAACACTTA[C/T]TAATTTAATTAACTC | 93664 |
rs185048416 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122840221 | ACTCATAGGTGGGAA[C/T]TGAACAGTGAGAACA | 93664 |
rs185053620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122321410 | TGGCCTCAAATGATC[C/T]TCACATCTCAGCCTC | 93664 |
rs185055856 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122632700 | ATCTCTTTAGATTAA[C/G/T]TAGGTCCCACTTGTC | 93664 |
rs185057209 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122435502 | TTTAAAATGAACAAA[C/T]AAACAAAACAAGAGA | 93664 |
rs185058777 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122715401 | TGGCAAAGTGGTGAC[C/T]TGAGCTTGTGAATAA | 93664 |
rs185059805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122516502 | ATGACCATGCCACTG[C/T]ACTCCGGCCTGGGTG | 93664 |
rs185065273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122495603 | TACAAACAATGCCAT[A/G]ATGGACATTCTTGTA | 93664 |
rs185067254 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122533422 | TTAATTTCAGAAAAT[A/T]CTCTTCTATTTTAAA | 93664 |
rs185070452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122396472 | AGGGGCTTGCTGAAA[C/T]ATGAAACTAAGAATG | 93664 |
rs185072237 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122742819 | ACTAGAGAGCTCTCT[G/T]AGCTTTGTTATAATC | 93664 |
rs185074934 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122720482 | GATATATGTATGTAT[G/T]TATATATGTATATGT | 93664 |
rs185078275 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122580567 | GACCTTTCACACAGA[C/T]TTACCTAATGTTAAT | 93664 |
rs185078598 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122721890 | GGCTGGTTCAATATA[C/T]GCGAATCAATAAATG | 93664 |
rs185084745 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122694977 | TTCAAAACCCGTTAA[A/C]TGTGGTGAAGGGGTT | 93664 |
rs185090826 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122750774 | GGTACGAAAGACCTA[C/T]CCCACACCTACTATT | 93664 |
rs185105739 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122768483 | AAGGTCTAGAAATCT[A/G]AAGGCTTTAGAAATG | 93664 |
rs185107756 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122732142 | CACCACATAGAAATA[A/C]CCAAAAAGATCTAAT | 93664 |
rs185122071 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122609581 | CTTTCACAAATTACA[C/T]TGCCTCACCGTTACT | 93664 |
rs185124094 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122635271 | ATTAATGTGTGGCTA[A/T]TTTTTTTTTTTAATT | 93664 |
rs185133708 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122853154 | ATGACTGAACCCTAT[A/C]AACTACAGTCCTAGA | 93664 |
rs185151288 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122575261 | GTATGATCCTGGATT[C/G]TATCCTAGACTGGGG | 93664 |
rs185153001 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122453593 | CTAGGCAAATTGATA[A/G]AAAGAGCAAATAACT | 93664 |
rs185153201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122666827 | GCAGATTCCCAGTGA[A/G]TTCTGCAGTGTGGCA | 93664 |
rs185157736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122417556 | GACATGAATGATCAA[A/G]TGTTTCATCTGTTTC | 93664 |
rs185165872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122413458 | ATGAAACCTGCTTAA[C/T]TGAGAAATTGTTGAA | 93664 |
rs185166188 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122838032 | GCAAAAATCCTCAAT[A/T]AAATACTGGCAAACT | 93664 |
rs185168154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122798895 | AATCTTCCTTTGTAG[A/G]AGGCTCTCATTAACA | 93664 |
rs185172209 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | CADPS2 | GRCh38.p7 | 7:122822837 | AACCCCCCTTTGACT[A/G]TAATTTTCCTTTACC | 93664 |
rs185174211 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122556057 | AGCCATAGCTGTGTT[G/T]AATCCAGCATATCTA | 93664 |
rs185176406 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122858686 | TTAATATTTGAAACA[C/T]GTTATATATAGTTGA | 93664 |
rs185179946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122857470 | AGATCCAATGTTACT[C/T]TGGGGAAAGGAGTGG | 93664 |
rs185182575 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122374722 | ATACTGGGGCCTGTC[A/G]GGGGCTGTGGGGATA | 93664 |
rs185186672 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122393043 | ATATGCTAAGCTTAG[C/T]TTACTAGCTTAAAAA | 93664 |
rs185187134 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122706455 | ATGCTTATATATTCA[A/T]GGAATATATATATGT | 93664 |
rs185190497 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122575839 | ACTATAGACGTTTTA[C/T]GTTTTAGAATAATTT | 93664 |
rs185194571 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122458332 | GATGAGGAAGAAAAC[A/T]ATAATCCCTTCTTTT | 93664 |
rs185195758 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122879726 | TCATTATAAAAATCC[A/G]TCACTAACTTGAAGG | 93664 |
rs185198763 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122422063 | GGAGATGGCTGAGGT[A/G]AGAAACACAAAAATC | 93664 |
rs185201490 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122498455 | TTCCTTTATTTAATG[C/G]CTTTATTCAAATCCT | 93664 |
rs185202042 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122354425 | TCAGCCTGTAAGTAA[A/C]CCCCCTGTTATGCAG | 93664 |
rs185207398 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122333245 | ATAATGTAGGATTTA[C/T]ATAAAAGTATATTGG | 93664 |
rs185210660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122353290 | GGTAAGAACCACCTT[C/T]TGGGGATTTTGAAAT | 93664 |
rs185211900 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122538979 | ATGTAGGTCTTAAAT[A/T]CTGGATGTTTAATGA | 93664 |
rs185214628 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122381806 | ACAAAAACAAACACA[C/T]ACAATGTTAAAAACA | 93664 |
rs185215775 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122518815 | TAAAATAAGTATCTA[C/T]CACACAGCATGAGAG | 93664 |
rs185225038 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122865181 | TCTTCTCTCACCATG[C/T]AATCTCTGCATACAC | 93664 |
rs185234209 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122887469 | TTCTGGCCTCAAGTC[G/T]GCGTCTTGTAGCTGC | 93664 |
rs185235916 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122481571 | GTGGAGAAACCCCAT[C/T]TCTATTAAAAAGACA | 93664 |
rs185236555 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122744138 | AGGAAACTGTAACAG[G/T]TGGCTAAAGTAAACA | 93664 |
rs185244128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122466266 | CAGGAGTTGCACAGT[C/T]TGAATGGAAGGTGTG | 93664 |
rs185264629 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122555400 | AACACAAGGTATTCT[C/T]CCCCTTTTAAAATCA | 93664 |
rs185267328 | snp | G/T | 0.0479149 | 0.147179 | intron-variant | CADPS2 | GRCh38.p7 | 7:122820563 | TGTTTTTTGTTTTTT[G/T]TTTTTTTTTTTTTTG | 93664 |
rs185271107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122618311 | GAGTCAATTGTGTGC[C/T]AGGCACTGTTTAGGC | 93664 |
rs185274043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122692824 | CATCCACAGCTCTCA[C/T]GCACTGTTCTCTCTG | 93664 |
rs185279845 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122650863 | CCAATTTACATTATG[A/T]TACATTTATTTACCA | 93664 |
rs185295639 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122733672 | TTGGGACTTCAGGAA[C/T]TCACCTGAACCCACC | 93664 |
rs185296361 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122559834 | CGAGAACCCTCTGGG[C/T]ACCACCTTTCTAGAG | 93664 |
rs185297462 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122437605 | TCCCTCTATTAGTTA[A/G]TCCTGCATGTATTAT | 93664 |
rs185302286 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122475174 | GCCTGTAGACCCTGC[A/G]GGTTTATCAAAAGGC | 93664 |
rs185303758 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122631372 | AACAGCTCTTACTTA[A/G]GTGTAAGTGAAATTG | 93664 |
rs185304302 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122752346 | TAAACAAAACATTCT[A/C]ATACTTTCTGGAAGA | 93664 |
rs185308171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122720956 | ATATATGTGCCAGGC[A/G]TTGTGTTAATTATGT | 93664 |
rs185313192 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122803440 | CTGTGATGGAATCTC[A/G]TTTTGGAGTCTGAAA | 93664 |
rs185313539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122597288 | CCTCACATAATTACT[C/T]GGAAAAAGAAATCAG | 93664 |
rs185323599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122781498 | ACTGTATTGTAATAC[A/G]TAAGAGATTTCACAT | 93664 |
rs185323608 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122418217 | AGCCAATTATGTGTC[A/G]GGCACAAGCCAGGGC | 93664 |
rs185323945 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122522409 | TGTGAGCCACTGCAT[C/T]TGGCCCCTTTTTATT | 93664 |
rs185332624 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122400467 | AAACAAAAACAAAAC[A/T]AAACTAAACAAAAAA | 93664 |
rs185332980 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122397419 | GGAGTGGGGGAGAAA[C/T]GGGGGAGACAAAGAG | 93664 |
rs185333352 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122378904 | CATCAAAGGTATTTT[A/G]AGCATCAAATTGGAA | 93664 |
rs185335374 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122818745 | CCTGCCCAGCAATTT[A/C]CTCTTAAAAAGGTGG | 93664 |
rs185336538 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122332090 | AAAAGCCCATTCAAT[G/T]TTTTTTGCAGGTTGA | 93664 |
rs185339929 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122358811 | AAGAAGGAATTCATC[A/T]CTTTGTAATCTGCCA | 93664 |
rs185343629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122362471 | CAAAAGTGGTTTACA[C/T]TTCTAAAACTTTATA | 93664 |
rs185345077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122664702 | GTCAAAAGACTCTCC[C/T]AGAAAAGCCTGCAGG | 93664 |
rs185352398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122338143 | GGCTCATGCCTGTAA[C/T]CCCAGCATTTTGAGA | 93664 |
rs185357547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122763147 | TGAGCACACAAATAA[C/T]CAAGTCATCATTTGA | 93664 |
rs185363611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122713629 | GACATAAAATATTGG[C/T]AAAGAAAAAAAAAAG | 93664 |
rs185363684 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122805316 | AGGCACTTGCCACCA[C/T]GCCTAGCTAATTTTT | 93664 |
rs185373511 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122726182 | TGTCAATGACAAAAA[C/T]GAATATTCTTGACAA | 93664 |
rs185376359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122837681 | CTAGAAAATCTACAA[A/G]AAATGGATAAATTCC | 93664 |
rs185376649 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122328903 | CACGGAAAACAGAAC[A/T]TCAGTCTAATCTAGT | 93664 |
rs185385885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122700206 | TTCTGACCTTGAACA[C/T]GAATGTCTCTGGTCT | 93664 |
rs185388314 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122613213 | ATTTTGTGTTTCAAA[A/G]TACAAATCAAGAAAG | 93664 |
rs185388832 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122735384 | CACTAAATTTGTGCA[C/T]TTTTTTTATTCATAT | 93664 |
rs185400446 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122775440 | TGCTGCATCTAAAGT[A/G]CATCTGTGTCACACC | 93664 |
rs185402869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122814946 | TCAGGCTCTGTTTAC[C/T]ATAACAAGCTGTGTG | 93664 |
rs185407153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122759527 | GATATGGTAGAGGTA[A/G]TGTTTCTGAGTTCTC | 93664 |
rs185407385 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122740916 | TCATAAAAAGAATAC[A/C]AATTAAAACTGTATG | 93664 |
rs185420551 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122579367 | CTAAGGTTGGGAAAC[A/C]CTGTAATAGATAGAA | 93664 |
rs185443856 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122706959 | GAATCATCATGATTA[A/T]CTTAGGTTAATCATG | 93664 |
rs185449537 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122502808 | ATTTATCTCTCAAAT[A/G]TCAGGAATTCTCCTT | 93664 |
rs185451611 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122541342 | GCTAGGATTACAGGC[A/G]CCCACCACCACACCC | 93664 |
rs185471124 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122595970 | TATCCAGAGGAATAC[C/T]AGCACTGCGGTCCAC | 93664 |
rs185480619 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122512585 | TCGTAAGCAAATACA[A/C]ACCAGTCAAGTTGAC | 93664 |
rs185481484 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122611358 | ACTAGAATCGGAAAC[A/G]GAAAAGAGGACATTA | 93664 |
rs185493935 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122352364 | TTCATTTTTAGCTTT[C/T]AAAGTTTAGATGGAC | 93664 |
rs185496654 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122475907 | TTACCTGAATGATTA[A/G]ATACATTACATGTGA | 93664 |
rs185497098 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122753934 | AAAGTTTAAAACAGT[A/T]GAATTTTAACATTAT | 93664 |
rs185498765 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122628901 | ATTATATGATTTTGC[A/G]GGGAGGAGTTTTTTC | 93664 |
rs185504294 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122556496 | AAAATTGGTATTGTA[C/G]CAAACTCTGAACTCT | 93664 |
rs185506012 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122722047 | GGACATATCTCAAAA[C/G]AATAAGAGCTATCTA | 93664 |
rs185519789 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122575866 | ATTTAAGACTTACAG[A/G]AAAGTTGCAAAGATA | 93664 |
rs185535545 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122796408 | GCCCAAATAGCCAAG[A/G/T]CAACCTTAAGCAAAA | 93664 |
rs185541983 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122837959 | CCTGATACCAAAGCC[A/T]GGCAGAGACACAACA | 93664 |
rs185544144 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122372606 | CAGATGTAGCAAATA[C/T]ATTTGTGAATATGCA | 93664 |
rs185554539 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122878791 | ACATTAGCCCACAAG[G/T]GGATTATTTGCTTGT | 93664 |
rs185582913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122676818 | AGATTCCGAACTCAC[C/T]GTAAGTGCTTGGTGA | 93664 |
rs185587939 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122613664 | GTTGGGGGTTGATAG[A/C]TAAAGGGTACAGTTT | 93664 |
rs185593313 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122493551 | GATTAGATAAGCAAA[A/G]ATGAAAATGGTTACT | 93664 |
rs185603789 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122647975 | ACCTTGTTAGTTCTT[C/G]TCTAAACCCACCTCA | 93664 |
rs185605763 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122836830 | ACACAATAATAATGG[A/G]AGACTTTAACACCCC | 93664 |
rs185607074 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122408948 | AGGCTGACTTAAGGA[A/T]GAACAGTGTAGTATA | 93664 |
rs185609037 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122589780 | GAAAATGAATGAGCT[A/T]ATGAAGGGTGCCCAC | 93664 |
rs185610848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122454634 | TCAGTTAAAGAAGAC[C/T]GTAAGAAAGGAAGTC | 93664 |
rs185616656 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122458741 | GAATAGGCCAAGGAC[C/G]AAAACATAATTGATA | 93664 |
rs185621207 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122675510 | AAAATTATCCAGTCT[A/G]TCACTGATGGGCATT | 93664 |
rs185621918 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122418628 | TATGGAAAGATGATA[C/G]TAGGAATAGAAAAGA | 93664 |
rs185622015 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122855167 | AAAAGAGGGTTGCTA[C/T]TTTCCTGGAGGGATC | 93664 |
rs185625902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122435983 | AAGAGAACATGAAGC[A/G]GTATTATTCACAGGG | 93664 |
rs185626054 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122875788 | AGGCCAAACTGCACT[A/T]AGAGATAAATTCATA | 93664 |
rs185629501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122659948 | AACAAGGACTTTCTC[A/G]AACAAAAACTGAGAG | 93664 |
rs185637906 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122550967 | ATGCCCAGTTTGGTT[C/T]TAAAAGGATGGAATC | 93664 |
rs185641093 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122645579 | TATATGCATATTCTC[C/T]AGGCTATAGAGATTA | 93664 |
rs185659632 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122358214 | ATTTGCATTTTCCTA[A/G]TGACAAATGATATTG | 93664 |
rs185680662 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122858025 | GAACAAAGCTTCCAC[A/G]GTGTGGAAGGGGACC | 93664 |
rs185684439 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122802739 | TAAAGCACGTGTCTA[C/T]TTTCACCATTAGCAG | 93664 |
rs185693899 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122632445 | GTGGCTTTGATTTGC[A/G]TTTCTCTGATGATTA | 93664 |
rs185694775 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122836433 | CACACATAACAATAT[G/T]AACCTTAAATGTAAA | 93664 |
rs185695030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122861810 | TACCATTATCTGTCC[A/G]TTCAAAACAAAATAA | 93664 |
rs185697389 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122819345 | AACTCTGGCCCAAGG[C/T]TCTCTGTCTGACTCC | 93664 |
rs185701113 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122803711 | TATGTCTGTGGGATC[A/G]GTGGTGATAAAAATT | 93664 |
rs185713073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122465894 | TTTGTACGTCAACAT[A/G]GATCTACAAATATCA | 93664 |
rs185714798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122480043 | GCATTTTGGTTGGAG[A/G]GAACAAAGTACAGTT | 93664 |
rs185718695 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122427736 | TTAGATAACACTTTT[C/T]TTTTTCTAAGTTGAC | 93664 |
rs185722809 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122705239 | GTCTAAGAGTCTTCC[C/T]GGAACCGCATGTGAC | 93664 |
rs185725900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122445384 | TTCTCAGCAATACTT[C/T]ATACTATTCAGTGTA | 93664 |
rs185729269 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122662830 | ATTTAATTACTTCCA[A/T]ACAACTCAGAAGACC | 93664 |
rs185730150 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122812225 | AAAGAGTTTCATGAC[C/G]CATTGATAGAAAACT | 93664 |
rs185732144 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122406330 | AGATATAGCAGTGGC[C/T]TTCTGGGATGAGAGC | 93664 |
rs185738299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122829922 | TTCCAAACATTGTGA[C/T]GTCCAGTAAGAAGAG | 93664 |
rs185740524 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122842784 | AAAATATAGCTAGAA[A/G]GTGTAAAGGAGGGAG | 93664 |
rs185742511 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122361104 | TCAATTTCTTCCATC[A/G]CACAAAAATTCACAA | 93664 |
rs185744670 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122339522 | ATTAAGAATAGCAGT[A/G]TTAATCTTACCAAGA | 93664 |
rs185746457 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122864355 | GGTGGTGGCATGTGC[C/T]CATGGTTCCAGCTAC | 93664 |
rs185748845 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122369423 | GGCGTGAGCCACTGC[A/G]CCCAGTCTTCCCCTT | 93664 |
rs185750941 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122387385 | TTTTATATTAAGCCT[A/T]GCTTCATGCAGTCAC | 93664 |
rs185756013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122503895 | GAAAATAATTTGGGT[A/G]ATGAATTGTTTTGCA | 93664 |
rs185758775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2, LOC105375481 | GRCh38.p7 | 7:122529605 | GAATGGGAGGAAAAT[C/T]AGCCTTTGGAAGAAA | 93664 |
rs185768819 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122531497 | TAAGAATGGGGCAAC[A/C]AAATTACCTACTTAT | 93664 |
rs185774349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122488927 | CTCTATGTGTATTAC[C/T]CAGAGGGTGAGAGGA | 93664 |
rs185776760 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122569093 | AGGAAGTCAAATTGT[C/G]CCTGTTTGCAGACGA | 93664 |
rs185785732 | snp | C/G | 0.000182408 | 0.00954833 | missense | CADPS2 | GRCh38.p7 | 7:122474418 | AGTCTGTGATCCAAA[C/G]TCTGCCTCTGGAGTA | 93664 |
rs185789800 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122508277 | TATATGAAGATTAAT[A/G]TACAAGAATTATACA | 93664 |
rs185790436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122377786 | TGTTGGTGAGTGTGT[A/G]AGGTATCTGTATCTG | 93664 |
rs185792870 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122432927 | TTACAAGGTAACCCT[C/G]CTAGGTTACCTTGCT | 93664 |
rs185797146 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122470273 | TTAGGATAAACAATG[G/T]AAATGTAAAAAAGAG | 93664 |
rs185802014 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122660710 | GGTCAGGAGATCGAG[A/C]CCATCCCTGCCAACA | 93664 |
rs185807495 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122337387 | GTGTTCCACGATCAC[A/G]TTTCAAGAATCTAAG | 93664 |
rs185810452 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122724334 | AAAAAAATTCACTTA[A/C]TTAATTATTTACTCA | 93664 |
rs185823143 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122835314 | AAGACCAAAGGTAGA[C/T]AAAACCACAAAGATG | 93664 |
rs185824440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122755885 | TCCAAAGAATCTTTG[C/T]GATGTAGACGTTTTC | 93664 |
rs185832054 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122883001 | TTTCTGTAAAACCAT[C/T]AGTGGTCAATCAGAG | 93664 |
rs185832136 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122818117 | GTAAGAACCCCCGAA[A/C]CCCTTCCCTCCATTT | 93664 |
rs185838370 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122777515 | ACAAGGTGACTGATA[C/G]AGTTTGGCTATGTCC | 93664 |
rs185838804 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122737813 | AGAGGAGCTTAGAGA[C/T]GAGGGAGGGATGCCT | 93664 |
rs185843501 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122871844 | AATACATCTGGCTAC[G/T]TCTTCTCCATTTCCT | 93664 |
rs185846084 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122806364 | CTACTACTGTACCCA[C/T]AGAACTAAAAACAAA | 93664 |
rs185856154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122641171 | TCCTTTCCTGGCAGA[C/T]AACATTTTACAGGTC | 93664 |
rs185857235 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122692226 | CTTGACTCCCGCAAC[A/G]TAGCGGGGGTGCAGG | 93664 |
rs185876824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122816567 | AGTGGAATTGCTGGA[C/T]CATACAGTAGTTCTA | 93664 |
rs185880876 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122363971 | AACCACTGGGATTCC[A/G]CCTGTTTCAAGGTTA | 93664 |
rs185884827 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122607368 | AGAGTACCTAAGGAT[A/T]GTGCTGTGGTAAGAA | 93664 |
rs185886459 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122672147 | ATAGAGTTTAAGACA[A/C]TCTTTCAGGCTTATC | 93664 |
rs185887144 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122834672 | GGGTCCCACACCCAC[A/G]GAGCCTTGCTCACTG | 93664 |
rs185897420 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122344057 | GAAACATAAAGCATG[A/G]AAGATAAAATTCATT | 93664 |
rs185898032 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122523297 | CTGTCACCTAGAAAT[A/G]AAACAACTAGAAAAA | 93664 |
rs185902007 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | CADPS2 | GRCh38.p7 | 7:122318201 | CTGACCAGCCAAGGA[A/G]GCCAATGGGCAGGTT | 93664 |
rs185913321 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122508927 | ATTGCATGGTTTGAT[A/T]TTTATCCTACACTGA | 93664 |
rs185927409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122703683 | AAGCCAGGGAGGTGA[C/T]AAATGTGTTTCAAAA | 93664 |
rs185931736 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122690573 | TCCCTACTTTTAGGG[A/G]TATTGGGGCAGGTAA | 93664 |
rs185932003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122449988 | TTTATAGTATATACT[A/G]TGAGATTTTCTCCTT | 93664 |
rs185933731 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122675776 | CTAAACAATGAGAAC[A/C]CATGCACGCAGGGAG | 93664 |
rs185940748 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122542387 | TCAGATATGATAGTA[A/C]GTCAAATGGCTAAAT | 93664 |
rs185947009 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122747372 | GCCTGTCATAAGCCA[C/G]AGAAAATTTCTACCC | 93664 |
rs185951087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122797396 | AAGACACACATGCAC[A/G]TGTGTGTTCACTGCA | 93664 |
rs185954779 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122754935 | TATTCTTAAGAACAT[A/G]GGAGAACTTAATTTT | 93664 |
rs185956522 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122718666 | CTGATCAAATGGGGC[C/T]GTGTTAAGGCTTTTA | 93664 |
rs185959157 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122817444 | CCTTTCATTTTCTGG[G/T]AGAGACAAAGGCGAC | 93664 |
rs185960844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122729872 | TGGTAACTGGAATGA[A/G]GAGGAGCAGCAGCAG | 93664 |
rs185962646 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122776529 | CTTTGAAACTGAGGA[A/T]CAGGCAGATTGGAAC | 93664 |
rs185970349 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122794478 | TTCTTTTCTATACTG[G/T]CTATTTTGTCTATCA | 93664 |
rs185970752 | snp | A/G/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122850345 | CTTCTCAGCCCTGCT[A/G/T]TGTCAGATCACCACC | 93664 |
rs185972709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122349241 | ATTAGTTTTTATTAA[A/G]AATATTGTATTCTAG | 93664 |
rs185989394 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122853974 | GAAAACGCCAGCCCT[C/G]TCCTTCCTTCAAAGA | 93664 |
rs186005068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122830465 | GAAGTGAAATACTCC[C/T]GAATAACATGCAACA | 93664 |
rs186012490 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122686076 | TCCACTTTTTTAGTA[C/T]ATTGATATCAGATCT | 93664 |
rs186022644 | snp | A/C | 0.0225045 | 0.103662 | intron-variant | CADPS2 | GRCh38.p7 | 7:122625217 | CACCACGCCCGGCTA[A/C]TTTTGTATTTTTAGT | 93664 |
rs186022983 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122619650 | TAAATAAATAAGATA[A/C]ACTCTTGTTGGAAAA | 93664 |
rs186031274 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122657162 | TGCTCTGTTCCATAG[A/G]TCTATATCTCTGTTT | 93664 |
rs186050918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122566672 | TATTTCAGGTAGAAG[A/G]CTAAACATACTAGAA | 93664 |
rs186053831 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122592174 | CATCACAAAGTGGGC[A/G]AAGGAGATGAACAGA | 93664 |
rs186057230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122588224 | AGTTTAATTAGATGC[C/T]ATTTGTCAATTTTTA | 93664 |
rs186058532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122530206 | TTAGTAATCTAAAAA[C/T]AAAATATATTTGTGA | 93664 |
rs186061386 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122602424 | AATGAACATCTTTTG[C/T]TCTGAAGCTATACAT | 93664 |
rs186069640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2, LOC105375481 | GRCh38.p7 | 7:122529865 | TAAATAATTGGAAAG[C/T]TAACAAGAATTGCAC | 93664 |
rs186075942 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122594816 | AATTGTAATCCAAGA[A/T]GTGACAAACAAATAA | 93664 |
rs186076718 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122560943 | CCCCAATATCAGAAC[C/G]CTTATAGTATGTGAA | 93664 |
rs186092487 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122547494 | GAGCATAATTTCTGC[A/G]TTCTATTCTTTTCTA | 93664 |
rs186096785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122370836 | GCTAGAGTTTAAGAT[A/G]TGGGGGAGAGTGTTA | 93664 |
rs186107834 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122325841 | ATATTCACGGAAACA[C/G]TGTTTTTGCACTTTG | 93664 |
rs186109886 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122812727 | ACTCTCTCCACCGTG[C/T]TCCCAACACATGATG | 93664 |
rs186118441 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122836482 | TAAATGACACAGACT[A/G]GCAAATTGGATTAAG | 93664 |
rs186132957 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122875368 | ATACTCATGAATCTT[C/T]ACACAACTAAGAGAC | 93664 |
rs186136182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122427892 | ATTATTAAGTCATCC[C/T]TCCTAGGTCATGGAA | 93664 |
rs186145958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122387666 | TTCTTTTATGTCACT[C/T]ACATTCTCTTTCAAA | 93664 |
rs186160976 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122849693 | TTTGATTGGGTCTTT[G/T]CATTCAAGGAGCTTT | 93664 |
rs186165202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122440589 | CAGTTGTAGTCCTCA[C/T]CTCCCAAGTTCTTAA | 93664 |
rs186165315 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122871210 | AAATTACACCCTGGT[C/T]TCATCCCACTTTTTG | 93664 |
rs186171045 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122838833 | AGGAAGAATCAATAT[A/C]GTGAAAACGGTCATA | 93664 |
rs186173096 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122403232 | TTTTGGATGGAAACT[C/T]GTGAGTTTGGGGTAA | 93664 |
rs186180457 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122424571 | GAGGCATAATCTTCT[C/G]TAAAGATCTTAAAGA | 93664 |
rs186182307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122469845 | TGTGTGTGTGTGCAC[A/G]TACACACATCTAGCA | 93664 |
rs186190219 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122713965 | GCACAATATTTTTCA[A/G]TATGTTGACAAAGAG | 93664 |
rs186194895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122384733 | GTGTGAATGTACAGG[C/T]GCACACATAATGAAC | 93664 |
rs186197392 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122523672 | AATATATGCATTACC[C/T]CAATATATTCTACCA | 93664 |
rs186197413 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122590444 | TCAAGTGTCAGAACA[C/T]GGATTTATGTAATTC | 93664 |
rs186197656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122510883 | TTGCCTTCCCATTAC[A/G]TTTGGAATTGAATGT | 93664 |
rs186200522 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122687155 | CCAATATCAGTACTT[C/T]CTAAATGGAAACATC | 93664 |
rs186202849 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122364527 | GTCAGGAGATCGAGA[C/G]CATCCTGGCTAACAC | 93664 |
rs186202977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122344201 | TTGCTGTTACGAAAA[C/T]ATTTGCCGTAACTTG | 93664 |
rs186207467 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122548168 | AGTCCAGGAGTTCAA[G/T]AACAGCCTGGGCAAT | 93664 |
rs186219000 | snp | A/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122532282 | ATCACGGGCAAAAAA[A/T]TTACCTTAAGTCTTC | 93664 |
rs186220980 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122484559 | TAGAAGAAAGCAAAG[A/G]AGAAAATGTTTGCAA | 93664 |
rs186227695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122552360 | AGATAATTGGGCTAT[A/G]AGGCATTTCTGGTCC | 93664 |
rs186235599 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122504258 | ATGTGGGAGTACCTA[C/G]CACAATGCATGCCTG | 93664 |
rs186239145 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122598340 | TAATAGCTTTAGAAA[C/T]GTTCAAATTCTAGCT | 93664 |
rs186241906 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122450393 | GAGAAAAAGAAAATA[C/T]GTTAGCATATTTCTG | 93664 |
rs186250703 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122445894 | GTAAGATTTTCTACT[C/T]AGATAATCATGTTAC | 93664 |
rs186254016 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122470940 | GACTCTACATAAAAC[A/C]CATTTTCTATCTTGT | 93664 |
rs186261209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122433562 | GCATGCACCCCCACT[C/T]CAAGCTAATTTTGTA | 93664 |
rs186264985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CADPS2 | GRCh38.p7 | 7:122885834 | GCAGCCGCATACCCG[A/G]CGGGTGAAAGCACCG | 93664 |
rs186267583 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122393692 | GACACAGAAGAACTG[A/T]TAAAATGCAGATGAG | 93664 |
rs186269814 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122414907 | TCTTGCTCATTTCAT[A/G]TGCTTCCTCAAGAAT | 93664 |
rs186281249 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122406691 | GCAGAAGAAAATACA[C/T]GACAGAAGACAACTG | 93664 |
rs186286564 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122717189 | TTTCACTTGTTATAA[A/T]TGTGAGTTAATTTTT | 93664 |
rs186288752 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122697191 | TTAAAATTTCACTAT[A/G]CAGATGCATATCACA | 93664 |
rs186290371 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122682291 | ACGGAATGGCAAATA[A/T]GAATTTCTAGAGAAA | 93664 |
rs186292238 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122668730 | AGAAATCAGGTCAAA[C/T]GAAGAGAGATTTGCT | 93664 |
rs186295847 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122672587 | CTTGAGGTCACACAC[C/G]TCCTGGGAGAATAGA | 93664 |
rs186296706 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122379206 | TGTTGACATAGTGTT[C/G]CTAACCTTTTTTTGC | 93664 |
rs186303253 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122728893 | TATTTATTATATTAC[A/C]AGTCGCCTCTCTTCT | 93664 |
rs186307774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122741305 | GCTTCCATATATAGA[C/T]AGAAACTAGGGAAGA | 93664 |
rs186310978 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122770134 | GGTCTCACTGAAGAA[A/C]TCAACCCTCAGCACA | 93664 |
rs186314125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122709191 | CTTCTGGGACTCCAT[C/T]ATTTCAAGATTGTCC | 93664 |
rs186316664 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122338872 | CTTGGATGATCCTCT[C/T]GCCTTAGCCTCCGAA | 93664 |
rs186319262 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122620200 | CACTGGGAACCAGCA[A/G]AGAGGATAAAAAGAA | 93664 |
rs186320425 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122811287 | GTCCTTTAGATAGTA[A/T]GTAGCATATGGCTGC | 93664 |
rs186331807 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122782142 | TAAAGAAAAGCTATT[G/T]ATATTGTGTATTTAC | 93664 |
rs186336208 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122653281 | GGGTAAACACATACA[C/G]AAGTGACACTGTTAC | 93664 |
rs186338801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122841721 | ATAACTAAAGAAAAC[A/G]AAGAGTTGCCTTAAA | 93664 |
rs186344988 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122638290 | AGCCCAGGGATCTCA[C/G]CCTTTTCAGTATTCT | 93664 |
rs186346176 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122700973 | AGTAGCTTTGGAAAC[C/T]AGATTTCCTGGGTAT | 93664 |
rs186356326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122603547 | ATAACGATTGGGTGT[C/T]CCTACCTATATTACC | 93664 |
rs186362194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122461196 | CAGCTGGAAAAATAC[A/G]TAGATAGAATACATT | 93664 |
rs186372266 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122587270 | TTTTCCTCCTCCCAT[A/C]CCACCCCATGACAGG | 93664 |
rs186379869 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122734053 | CCCCATTCTCAGAAA[G/T]TCTTATTCAACAGGT | 93664 |
rs186389592 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122619478 | AAAAAAAAAAAAAAT[C/T]TAGCCAGGCATTGTG | 93664 |
rs186391942 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122581351 | TTTTCCCCAAGGAGA[A/T]GTGTCTCCATAGAAG | 93664 |
rs186396506 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122770413 | TCACTTTAAAGAATA[C/T]AGTGAGAAGGATCAC | 93664 |
rs186398338 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122547075 | CTCAAATCTAGGGTG[G/T]TTTTTTTTTGCCTTT | 93664 |
rs186403944 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122482178 | TGTTAAGAAAAAATA[C/T]GGGAACACAAGTGAA | 93664 |
rs186408687 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122648830 | CCAGCAGCCTAAGAA[C/T]TTCATAGGCAACACA | 93664 |
rs186409809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122752723 | TTCAGAACTCTTTCC[C/T]TGTGAAACTTCCTAC | 93664 |
rs186409999 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122793265 | GTGTGGGAGTCTAAG[A/T]CTCTTGAGAAATTCT | 93664 |
rs186411901 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122616188 | ATTTAATTTATAAAA[G/T]AGATTAAAATGCATT | 93664 |
rs186419477 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122863922 | GTAATCCTAGCTACT[A/C]GGGAGGCTGAGGCAG | 93664 |
rs186422775 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122428471 | TATATATATATATAT[A/T]TTTTTTTTTTTTTGA | 93664 |
rs186436927 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122398497 | AAACAAACAGACAAT[A/C]CAAATCACAATAAAA | 93664 |
rs186441597 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122519614 | CAAAGAAACACACAA[C/G]TGATTGCTAGGAAAC | 93664 |
rs186445297 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122624665 | TCTCTCTTCCTTTCA[A/G]TTCAAATATGCCTTT | 93664 |
rs186446758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122582414 | GACTGAAGAAACTGG[C/T]ATCTAGATGCAGTCT | 93664 |
rs186449670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122599119 | CAGGAATGGGACCTG[C/T]TCCTAGTAGGGACAA | 93664 |
rs186455964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122617195 | AAACAGTACTCTGCT[C/T]TTCAAAACAATACTT | 93664 |
rs186461260 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122640851 | AGGCAGAAGAATGGC[A/G]TGAACCCGGGAGGTG | 93664 |
rs186462721 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122434579 | GGTGGGTGCTGGGAA[C/T]ACAACAGTGAACAAG | 93664 |
rs186467307 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122446398 | CAGTTTGGCCTATTT[A/G]AATCTTGATTTTAAT | 93664 |
rs186467826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122359596 | GTCCAATGTGATATA[C/T]ACAAGATTATTTGTG | 93664 |
rs186468758 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817868 | TTATTTCCATGCCCC[A/G]ACCTCTTATCTCTGC | 93664 |
rs186470956 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122860667 | ACTCTACTATGCAAT[A/G]GAATATCAGGATTTC | 93664 |
rs186471148 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122881195 | GAGCTGTTTCCATTA[A/C]AGGCAAACAAAACGA | 93664 |
rs186477520 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122415688 | GCAGAATAGCTCTGA[A/C]AGTTGCCTTAGGGTC | 93664 |
rs186479038 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122764422 | TTAATTTGAAAAATA[G/T]TTAGTTCCTACAATG | 93664 |
rs186485227 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122729469 | GTAGAGGTTGTACTA[A/G]TTTACATTCCCACCA | 93664 |
rs186489483 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122395664 | ACTGATATCTGAATT[C/T]ATTGGGTCTCTACTT | 93664 |
rs186492190 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122377023 | GTAAACTTATTTTAT[A/G]CTTTTCAACCAAAGA | 93664 |
rs186496465 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122356385 | CATTTTCATCACATC[C/G]TGTCAAAGGCTGATA | 93664 |
rs186498314 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122760616 | GCACATATACACCAT[A/G]GAATACTATGCAGCC | 93664 |
rs186502292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122726308 | TTTATAAACAAAACC[A/G]ATAGTGTACTAGGAA | 93664 |
rs186511517 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122790945 | AGGTACATAAAGAAA[C/T]GGTAGCACCCAAAAT | 93664 |
rs186514507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122828536 | CTTGAGTATTATATG[A/G]CACTACAATTTTTGT | 93664 |
rs186520177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122335571 | ATATAGGGAATATAT[A/G]GAACTATAGAGGTCA | 93664 |
rs186520802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122703351 | TGGGATGGTTCAACA[C/T]TACCGAATATGGCAT | 93664 |
rs186541269 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122474601 | AAGAATACAAAATGC[A/G]TGACTCAAGCAGAAG | 93664 |
rs186563288 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122685104 | AATGTTATTGCTTTT[C/T]AATCCCAGAATCTGA | 93664 |
rs186564049 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122436253 | ATCAAGTTGTGTACA[G/T]TAAATATGTACAGCT | 93664 |
rs186565788 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122839503 | AGACAACCTACAGAA[C/T]GGGAGAACATTTTTG | 93664 |
rs186567871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122671748 | TTGATACAGGAGGCA[A/G]TGGAAAACACGAAAG | 93664 |
rs186568714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122825030 | TCCAATAGCCAAAAA[C/T]TAAAAACAATCCACA | 93664 |
rs186571850 | snp | G/T | 0.0733688 | 0.176922 | intron-variant | CADPS2 | GRCh38.p7 | 7:122657080 | AATCCTTTCCCCATT[G/T]CTTGTTTTTGTCAGG | 93664 |
rs186581874 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122498150 | ACGGGGGTTCACCAC[A/G]TTGGCTAGGCTGGTC | 93664 |
rs186592265 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122699880 | TCATTTTTTAAAAAA[C/G]AGCTATTAAGAAAAA | 93664 |
rs186593148 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539307 | CATGTGACGCCTTTC[A/G]CCATATTTTAATACA | 93664 |
rs186595443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122712940 | CCCACCTCCTAATAC[C/T]ATCACCTTGGGGGTC | 93664 |
rs186598852 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | CADPS2 | GRCh38.p7 | 7:122398792 | CCACCCCTCACCCCT[C/T]CCTCCCTCCCTGAGA | 93664 |
rs186599346 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122601213 | ACACTCAAATATTAA[A/G]ATTTTTGAAGATTCT | 93664 |
rs186602675 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122636882 | GTATTTCTTAAATTT[A/G]TACGTCCAACTCTCT | 93664 |
rs186609135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122499958 | GCTGGGAGAGAGATG[A/G]AGGGCATGGGAAGGT | 93664 |
rs186643749 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122566215 | ACACCTGAATGGCTA[C/T]TACCAACAAGATAAA | 93664 |
rs186645902 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122466700 | ATCGTTTAAAAAGTA[C/G]TTACAGAATTTTATT | 93664 |
rs186657726 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122726848 | CTAACTATAGGTGTT[A/C]AAAGAAACATTACTT | 93664 |
rs186663278 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122746901 | GTAACTAAGAGAGAA[C/T]TGGCAAGTCTTGTTG | 93664 |
rs186663744 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122742528 | TGTACTAGATAGACT[C/G]ATCACCATTCTCTTA | 93664 |
rs186667130 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122715221 | ATTGTCTGAGTTTTC[A/T]TACCGATATACAGGA | 93664 |
rs186668138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122637718 | TAATGTGTTTGTTTC[A/G]GCATAAAGAGACACT | 93664 |
rs186675533 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122343356 | CCCATAGCCATGTCA[C/G]ATGCTTAGGCATTGA | 93664 |
rs186683668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122762126 | ATATATGTATATGTA[C/T]ATATAAAACAACAGA | 93664 |
rs186686276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122696830 | TAACACATAATAGTT[A/G]CATTACAACAAAGAT | 93664 |
rs186688985 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122617988 | GCGGAGGTTGGCAGT[G/T]AGCCGAGATCGTGCC | 93664 |
rs186689354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122805070 | TACAAGTTTCTTAAG[A/G]ACAAGAGCCACATGA | 93664 |
rs186693407 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122574021 | AATCAAATGGCAAAA[A/C]AAATGTTTATCTTTA | 93664 |
rs186693949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122668192 | TAGAATGAATGTGTC[C/T]TGGTAATTTACAAAA | 93664 |
rs186696220 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122783088 | GTGGTGGTGGGCGGG[C/T]GCCTGTGGTCCCAGC | 93664 |
rs186702614 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122784725 | TTTAGTATTTTTTTT[C/T]TCTGGAGCCATCTGT | 93664 |
rs186704506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122593746 | AAAGAGAGAGAGCAA[C/T]AGAGACGTCAACTAA | 93664 |
rs186725880 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122649967 | CAGGCTGGAGTGCAG[C/T]GGTGTGATCTCGGCT | 93664 |
rs186733017 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122634463 | GTAGCATATACAGAG[G/T]TTTTCAAAATAATCT | 93664 |
rs186734733 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554255 | AAGAATGTTTCTTAG[A/G]AGGTATCAGTGCCCT | 93664 |
rs186741203 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122599734 | TATTCTTTCACAGGT[G/T]TAGGCCCTTTGTAAA | 93664 |
rs186746509 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122718255 | TGACTACTCAAAGAA[A/C]TGCCTGTCAGCATTC | 93664 |
rs186757564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122355346 | AGGACTTTGGGATGC[C/T]GAGGCAGGCGGATCA | 93664 |
rs186761274 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122383591 | GTGCCTGCTTTCCCG[C/T]AGGTGATTCTGAACT | 93664 |
rs186766573 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122689990 | ACTGTCCACGAGGCC[C/T]GGACAGTGTGCAGTT | 93664 |
rs186766671 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122518534 | TAAACATATAGAAAA[A/G]TATTATCTAAGAAAT | 93664 |
rs186775178 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122456000 | GAGCCACCATGCCCA[C/G]CTTGGAACATTTTTA | 93664 |
rs186778867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122785307 | AGATTGTATGATTTT[A/G]TATACTTATGTAGAT | 93664 |
rs186787221 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122819784 | AAAGCCTCCTTTGCA[C/T]CCTCCTCTTGTATCC | 93664 |
rs186789543 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122436892 | TATCTTTTCTGTATC[C/T]GTGGACAAGTTAATA | 93664 |
rs186790933 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122489576 | AAAAGTGACATGTCT[C/T]TAAGGTACAAGGGGA | 93664 |
rs186791995 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122823513 | TGTGCATAGAAGTCT[C/T]TTGGAGAGCGTGCTT | 93664 |
rs186800904 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122858969 | AGAATTACATATTGA[A/T]TTGGTCAGGGAACAG | 93664 |
rs186803364 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122399871 | TTTTGTATTTTTAGT[A/T]GAGACGGGGTTTCAC | 93664 |
rs186803452 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122420302 | TCAAAATCAGCTATT[A/G]CATGTGACACTATCT | 93664 |
rs186806541 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122837437 | TAAGATCAGAGCACA[A/G]CTGAAGGCGACAGAG | 93664 |
rs186812258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122455332 | TCAGCATTAGTGAGG[C/T]TATCTCCAACCATCC | 93664 |
rs186815640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122419169 | TAATGAATGTTTACT[A/G]AGAATGCAGCAGAAT | 93664 |
rs186817346 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122381380 | TCTTACATGGAAAGT[A/G]CTCCAAAGCATGCAG | 93664 |
rs186819034 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122329647 | CTTTTTACCTAATTT[A/G]TAACATTTTGAGGAT | 93664 |
rs186819436 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122361261 | TAAAATGAGATGGAG[G/T]CTTGCTCTGTCACCC | 93664 |
rs186826610 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122340254 | ATCTTGTGGAGATGA[A/G]ACTCCTCCACAATTA | 93664 |
rs186831715 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122381116 | ATGGGTAGGGTAATC[C/T]CTCCACAGACACACT | 93664 |
rs186837800 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122657435 | ATTGATTCTTCTATC[C/T]ATGAGCATGGAATGT | 93664 |
rs186839433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122723330 | AACTCAAACAAATTT[A/G]CAAGAAAAAAAACAA | 93664 |
rs186840315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122694350 | AAGATGCTGTGAGTT[A/G]TTAAGTTTTCAAAGA | 93664 |
rs186848670 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122679395 | AAATTCCAGCCTGGC[A/G]AATTCTAGTCAGACC | 93664 |
rs186860401 | snp | A/C | 0.0023933 | 0.0345097 | upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122886890 | GCCCGTGTAAGCGTC[A/C]ACCGGGGCTGCTCCG | 93664 |
rs186863860 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122348381 | AAGCCTGAAAGAAAA[C/T]GAAATGCTTTTCCTA | 93664 |
rs186864558 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122666504 | ACGTGCCACCATGGC[C/T]GGCTAATTTTTATAT | 93664 |
rs186872542 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122592831 | ATCACACACTGGGGC[C/T]TTCCAGGGGGATGGG | 93664 |
rs186872624 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122652795 | AATCTAGGTGCTACT[G/T]ACATTGTTTTTATTC | 93664 |
rs186881226 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122607655 | CATCATATTTTCTTA[C/T]TAATTCAGATGCCTC | 93664 |
rs186883319 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122561528 | GATGTGTCAATCATT[C/G]TCCAGTTTTTCCTGA | 93664 |
rs186887111 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122625860 | ATATTATATACATAT[A/T]TATTATATCTACCTA | 93664 |
rs186893157 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122483095 | CACTGCTTGGTCTTC[C/T]CTAACAAAACTTGAA | 93664 |
rs186899788 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122506080 | AAGATTAGCAGGGTC[A/G]CCCTGCTCCCTGTGC | 93664 |
rs186900122 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122553860 | CCTATGCTGGGATTT[A/G]GCCATAGTAAGTCCA | 93664 |
rs186902083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122571988 | GCCTTTCCTTAACTC[C/T]CACAGACAAAATTTA | 93664 |
rs186905127 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122501577 | CACCTTGGCCAGGCA[C/T]GGTGGTACATGCCTG | 93664 |
rs186907391 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122544886 | CAAATAACTTTGTAA[C/T]TCACTTATCTCCCCC | 93664 |
rs186909940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122526752 | TTGCTAATTAGGTCA[C/T]ATTCCTTTATTATAC | 93664 |
rs186910962 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122682029 | TATCAGCTAATAGCA[A/G]ATCTTTGAGTCTTTC | 93664 |
rs186914946 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122629579 | CAAGAAATTAGATTT[A/C]TTGATCATTAAGTCA | 93664 |
rs186941715 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122460743 | AAAATGGAATCAAAC[C/G]AAGAAAGGAAAAAGA | 93664 |
rs186950920 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122494837 | TACTTTTTCCCTTGC[A/G]TATGTCTAAGGTTTA | 93664 |
rs186951713 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122837521 | GATCAACAAAATTGA[G/T]AGACCACTAGCAAGA | 93664 |
rs186958208 | snp | A/C | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122820205 | TTCCTTTGCACCCTT[A/C]ATCCCAGCCTCTCTT | 93664 |
rs186976077 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122402679 | TTAGTAATTTTAAAT[C/T]TTGGGAAAGCAAACA | 93664 |
rs186977446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122764939 | GTAGCCCAGGTATTT[C/T]ACTAAATAACTTTGC | 93664 |
rs186978596 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122868737 | TGAAGCTTATGCTAA[C/T]GAATGGAGATATGTT | 93664 |
rs186980527 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122334360 | CCATGGGGTGTATTA[A/G]GAGGCATGGCTGGAT | 93664 |
rs186981056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122424105 | GATGGTATAGCCTCC[C/T]GATAGGTATTTAAAA | 93664 |
rs186982205 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122807994 | TAAAACAAATCCAGT[A/T]CAGATAGCTCTAAAC | 93664 |
rs186996011 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122836584 | AAAGGGATGGAGGAA[C/G]ATCTACCAAGCAAAT | 93664 |
rs186998324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122689710 | TACAAAGTCCACTGG[A/G]GCCCAGCCTTGGTAA | 93664 |
rs187014646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122680085 | CTCTGTCATAATCTT[C/T]GCAAAGGCAGTTTTA | 93664 |
rs187015252 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122838586 | TCAGCAAAGTCTCAG[A/G]ATACAAAATCAATGT | 93664 |
rs187021450 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122549421 | TTTTGTAGTTACCAT[A/C]GCACTCAAGACATTC | 93664 |
rs187025913 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122736762 | ATTTCGATTCTGTTT[A/C]TCTCTCAAAACCAGG | 93664 |
rs187029969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122708129 | CCCATTTAGAAAAAA[C/T]CCTGATATAATTCCC | 93664 |
rs187037914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122511619 | AAGTTAGCTGGGTTT[A/G]TTCCCAAACTAGTTT | 93664 |
rs187043603 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122628437 | TTGTATACATGTTAC[A/G]AGAGAGAGAAATAGA | 93664 |
rs187059588 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, nc-transcript-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122530522 | AACAACTTACCTTTC[A/G]AAAGATAAATTTTCT | 93664 |
rs187061350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122857124 | AAATATTCAGGATAC[A/G]ATGCTAAGGGAAAAG | 93664 |
rs187061856 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122567949 | ATATCAATATTCATA[A/T]TAAAATATAATTGAA | 93664 |
rs187074032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122491694 | ATAGAAGCACCATAA[A/G]TAAGTATTCATGTTG | 93664 |
rs187074495 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122543467 | CAATAAATTTACTCA[A/T]TTATTGAGTCTGACA | 93664 |
rs187075559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122877868 | TTAAATTATCAACAT[C/T]TTACTGAAGGAGTAG | 93664 |
rs187077395 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122458153 | TAGGGAAAGTGAGAA[A/G]GGGAGAGACACCTAG | 93664 |
rs187078812 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122475016 | TGTAAAAATGGCAAT[A/G]AGCGCTCTCAAGCTT | 93664 |
rs187082120 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122795277 | ACAACAAGGGGGATA[C/T]TACCACTGACCCCAT | 93664 |
rs187084077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122659772 | AGGGGGAAAATAACA[C/T]CTTACCTCTAAAGAG | 93664 |
rs187089789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122437281 | TCTCGTGATATAATG[C/T]TGGTTGTTATGGTGA | 93664 |
rs187092775 | snp | C/T | 0.00260775 | 0.0360149 | missense | CADPS2 | GRCh38.p7 | 7:122388719 | TCCAAAAAAGGTCTT[C/T]TGATGTTGCTGAGCC | 93664 |
rs187095788 | snp | A/C/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122371073 | AGTGTTCCCCAAATG[A/C/G]GTTAGTAACCTCATC | 93664 |
rs187099826 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CADPS2 | GRCh38.p7 | 7:122350816 | CATGGCAAGACCCTG[C/T]CTGTATAAAAAAGTA | 93664 |
rs187107577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122513944 | GTAACGAAGATGCCA[C/T]TGGGTAGTTTTACAT | 93664 |
rs187113463 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122327148 | AAAAAAGTAAACTTC[C/T]AGTAAATTCAATACT | 93664 |
rs187114833 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122449769 | TATGCTATCTACAAC[A/G]GTGTTTCCTAATGTA | 93664 |
rs187124029 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122721844 | AAAGCTTATCCACCA[C/T]GATCAAGTGGGCTTC | 93664 |
rs187124821 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122412673 | ATCGTATTTAAAATA[C/T]TTTAAGGATCTTAAG | 93664 |
rs187127585 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122477001 | GGGAGGGGAGGGGAG[A/G]GGAGAGGAGAGGAGA | 93664 |
rs187127617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122694635 | TAGGAAAGAGACCAT[C/T]TGTTTTTCTAAAGTA | 93664 |
rs187128185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122880737 | AGTTAAGATAAGAAT[C/T]GCACTTCTTTTTCCT | 93664 |
rs187129237 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | CADPS2 | GRCh38.p7 | 7:122706329 | ATATATATATATGCT[C/T]ATATATTCAAGGAAT | 93664 |
rs187131482 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122880580 | TATCTTCTCTTTAGA[A/G]CAGCGGTTCTCAACC | 93664 |
rs187145349 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122773619 | AGAGCTGTAGGATTC[A/G]TACAAACTATTTTTA | 93664 |
rs187145648 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122374369 | CACTTACCACTTCTA[C/T]TCAACATAGTACTGG | 93664 |
rs187153784 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122439861 | ACTATTATACTTCCC[A/G]TGGCAACAAACTTTA | 93664 |
rs187155107 | snp | C/T | 1.6985e-05 | 0.00291414 | missense, utr-variant-5-prime | CADPS2 | GRCh38.p7 | 7:122736968 | ACCTCATAATAACTC[C/T]GAACTGCGTTGCAAA | 93664 |
rs187157677 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122332532 | TAAGAGTATCATGTC[C/T]ATTAAGGAATGAAAA | 93664 |
rs187158782 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122776871 | ATAATAACAAGAAGG[C/T]CAGGTGCAGTAGCTC | 93664 |
rs187165599 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817058 | ATAAAACGGCCCCAC[A/C]CATATCTCCCTTCGC | 93664 |
rs187169133 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122375418 | CAATAGAACAAAACA[C/G]AGAGCTCAGAAATAA | 93664 |
rs187170906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122734573 | TGTTCTGGTAAACTA[C/T]AAAAATTACTACATA | 93664 |
rs187175570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122753739 | ATTAGATGACAAATC[C/T]AAAGCAAGCTCAGTT | 93664 |
rs187208331 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122702968 | ACTTGTGATTGGTAC[A/C]ATGTGATTTCAAGAA | 93664 |
rs187212371 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122723919 | CATTCTCAGCAAACT[A/G]TCACAAGGACAGAAA | 93664 |
rs187219390 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122591276 | TAGGAATCCAACTTA[C/T]AAGGAATGTGAAGGA | 93664 |
rs187234631 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122645395 | TGTACATGTGTGTGT[A/G]TATATGTACATATAC | 93664 |
rs187251608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122515360 | TCTTCTCTGTGGTTC[C/T]AGTGACAGGTATTTA | 93664 |
rs187258209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122610093 | GGGGAAACACAGAAA[A/G]GCTATTTTAAATTAA | 93664 |
rs187262083 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122674796 | TGTGTTCAGCAAAAC[A/G]CTGAGAAAAGTACAA | 93664 |
rs187262583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122691644 | ATAGTCCTGCAGTGA[C/T]ACTATGAAAGTCCAT | 93664 |
rs187264209 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122710410 | ATTAAAGCACCAGGC[C/T]GTGTGACAGATGTGT | 93664 |
rs187265153 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122588489 | TTGTCAGGTTTGTCA[C/T]GATGAAATTTTTAAA | 93664 |
rs187275003 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122552583 | TGTCTCACCTATCCT[A/G]GAGTATGCTAAACCA | 93664 |
rs187281637 | snp | C/T | | | intron-variant, synonymous-codon | CADPS2, RNF133 | GRCh38.p7 | 7:122698007 | AACCACTTGAATCCC[C/T]AAAACTTTAAGAATA | 93664 |
rs187282995 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122676405 | ATGAGAAAACAAGAG[C/T]CAAATGTTTGTCTTT | 93664 |
rs187288734 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122661899 | AAATACAAAGTTCCA[G/T]TTGAAGTTATCTTTC | 93664 |
rs187292711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122605176 | TACCATGAAAGGAAA[C/T]TGCAGGACGGGAAGT | 93664 |
rs187293355 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122860322 | CAGATTCCAACTTCC[A/G]GTTCAAGTGATCACC | 93664 |
rs187297539 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122621793 | AAATTGTATGATATA[A/T]ATACTTCACTGTCTT | 93664 |
rs187305172 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122639480 | TCCTGACTTTGGCTA[C/T]GTAATCACCCATCTA | 93664 |
rs187311503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122613045 | ATACAAAAATCAACC[C/T]AAAATGGATCAGTGA | 93664 |
rs187312478 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122477571 | ACAAAAAACAAAAAA[C/G]CAAAAACTGTAAAGT | 93664 |
rs187316496 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122568881 | TTGAAATATGATTAA[A/G]AGAATAACGAGAGCT | 93664 |
rs187317279 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122324607 | AAACTACTGTGTATA[C/T]TCATATATACACACA | 93664 |
rs187319533 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122589255 | ATTATCTCCTTTTAA[C/T]TGAATAATGTAACAA | 93664 |
rs187326845 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122706076 | AGGAATATATATATG[C/T]TTATATATTCAAGGA | 93664 |
rs187328516 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122431375 | TGCACTATACATTGT[G/T]TTGGATTATAATAAG | 93664 |
rs187330233 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122392273 | GATGATGCCTGATGA[C/T]AGTAATAATAACAAA | 93664 |
rs187331405 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122759387 | ATTGAAATGCAAAGG[C/T]TAGGAAAGAAATCAA | 93664 |
rs187332465 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122647630 | AGTTTAAAGCAAAGA[C/T]AATTTAAGATATTTT | 93664 |
rs187338175 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122579072 | GGAAATACTGAGTAC[A/G]GAAGTTGGATACACA | 93664 |
rs187340167 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122631005 | ACTGTGTCTAAAATC[A/G]AAATGATTAAAATTA | 93664 |
rs187340653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122596938 | GTCCAGTGAGGGCAT[C/T]AGGCTGCTTCCACAC | 93664 |
rs187342226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122531072 | AAAGTCAGCAATCTT[A/G]AGAGAGTACAGTGTC | 93664 |
rs187344576 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | CADPS2 | GRCh38.p7 | 7:122319403 | CAGAAGTAGTTATGA[A/G]CAAATAGATTTTTAT | 93664 |
rs187348986 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122447580 | TTTTTTTGAGACACA[A/G]TGTCACTCCATCACC | 93664 |
rs187353855 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122847052 | GCTCTAATCACCTCA[A/G]TTGTCTCCCTTCTCC | 93664 |
rs187355153 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122467326 | TTTGATGATCCTACG[G/T]GATGCAATTATCTAC | 93664 |
rs187355188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122833096 | CTACTAACATCTTCA[C/T]ATTTCCTTCCAGCCT | 93664 |
rs187358477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122353568 | AGAGTTGGTATGCAG[C/T]GTGTGTGATAATGTT | 93664 |
rs187363413 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122755313 | GGCTATGAAGTTTAA[C/G]ATCTTCAAAATTATT | 93664 |
rs187370079 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122428880 | AGCATTTGTGTGACT[A/G]TCTGCATCCAGGGCC | 93664 |
rs187372911 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | CADPS2 | GRCh38.p7 | 7:122381836 | AAAGGAATAAAGAAG[C/T]ATACATCTGAAATTT | 93664 |
rs187373337 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122866959 | ATGCTAGCCACCCTG[C/T]ACAACTTTGCTGCTT | 93664 |
rs187374918 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122797615 | AAAACTAAATACCAC[A/G]TTATCATTTATAAGT | 93664 |
rs187375335 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122834821 | GCCCACCGCAGCTCA[A/T]GGAGGCCTGCCTGCC | 93664 |
rs187379344 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122649594 | TCTATTCATTCTAAT[A/G]TGCATACAAAGTTGG | 93664 |
rs187382486 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122409029 | TGACCAATATATGAA[A/T]GTGAAAACTGGTTGG | 93664 |
rs187389239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122389480 | ACAGGAGTGCTATCA[C/T]CCCATGTATGAAGAT | 93664 |
rs187407219 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122725978 | CCGTGTCCCTAAAAA[G/T]AGTTGGTGTCTCCTA | 93664 |
rs187410403 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122796031 | AGGATACAAAATCAA[C/T]GAGAAAAAAATCACT | 93664 |
rs187412854 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122678763 | AATCTTGTGACCTCT[G/T]GCCATAGGACTACTG | 93664 |
rs187426815 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122571471 | ATCAGCCCCTGTAAG[A/T]GGTGATAAGGAAAGA | 93664 |
rs187428863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122814454 | GGTCAGCAAACTGGT[C/T]TTGTGTGTCCTGAAA | 93664 |
rs187435583 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122654896 | ACACTTGTGATTCAA[A/G]GGAGGAAGTTAAAAT | 93664 |
rs187436721 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122606646 | TCATAGTCTGAGACC[C/G]ACTGAGAGGCTTTTT | 93664 |
rs187458800 | snp | A/G | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122873637 | AGTAAACGTACGTGT[A/G]CATGTGTCCTTATAG | 93664 |
rs187472615 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122404133 | ATCTCCTAATGCTAT[A/C]CCTCCCCCCTCTCCC | 93664 |
rs187475524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122487763 | CAGGTATGGATCTGG[A/G]GGCATTCTATGTTTC | 93664 |
rs187480781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122473085 | AGCTGCCTCCTTACA[C/T]ATTTTAAGTTCAGCC | 93664 |
rs187484569 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122365089 | GCAGAATTTTCTCCA[C/T]GTGGCATCTGGCAGC | 93664 |
rs187485132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122435112 | GCATTTTCAGAATTC[C/T]TAATCAAAATGATCT | 93664 |
rs187498269 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122533071 | CTCTTGCCCTCTAGA[A/G]ATGTGGGGCTAAGTA | 93664 |
rs187499103 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122766639 | TGAAACGCCATCTTG[C/T]TCACAACTAAGAAAA | 93664 |
rs187500964 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CADPS2 | GRCh38.p7 | 7:122320058 | AAGAAATACAAGCAT[C/T]TTTATTTGGCCAAAA | 93664 |
rs187503546 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122482611 | TATTAAACGCTGCAC[A/G]TTGGGCAACGTGATT | 93664 |
rs187507817 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122808654 | AGTTCAGATATCTCT[A/G]AACAGAGGTATAGTA | 93664 |
rs187515279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122500810 | AAAATATCTGACTTA[C/T]GTAAGTGGCAAGATA | 93664 |
rs187517617 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122719980 | CTCAATAAAGAGTTA[C/T]TGGAATGGAAACTCT | 93664 |
rs187532993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122705040 | AACCCCGATGGGTGG[C/T]CAGGTATAAATTCTC | 93664 |
rs187535502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122608662 | CTTCTTGTCTTTTTA[C/T]TACTTTCAGGTGGTG | 93664 |
rs187536267 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122799314 | AAGAAGTATAGCTAT[G/T]TAGGGCTGGGCGCGG | 93664 |
rs187540553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122778371 | TGCCTGATGATATAA[C/T]AGAAAAGAAAAAGAA | 93664 |
rs187543821 | snp | C/G/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817536 | TTGGTGTTTAATCAT[C/G/T]GCAGGGACGCCTCTC | 93664 |
rs187544939 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122584670 | AAGCCTTTCTTCCAT[G/T]CCGGGCAAGCATTTG | 93664 |
rs187545395 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122731970 | TACTTATAATACTTA[A/G]GACATCTTATTAAAA | 93664 |
rs187548400 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122767847 | TAGTAGAACGTAGAT[G/T]ATCTGCATTGAAAAT | 93664 |
rs187551404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122750183 | AGTCTCAACAGTATG[C/T]CATGGCCCTTCTTTC | 93664 |
rs187558044 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122670080 | CTCTCCCTGGGGCTC[A/C]AGGGATGACAGCAAA | 93664 |
rs187563240 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122505566 | TATCTAAAATATCAT[A/C]CAACAGACCTAGACT | 93664 |
rs187564365 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122655496 | GCATTTTTTAAAACA[A/G]GAAAGTATTTTTAAA | 93664 |
rs187565336 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122495043 | TTGTTCTAAAAAGAA[A/G]TCCTTTCTCTTACTC | 93664 |
rs187566489 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122544487 | TATTAAGCAGTTCTA[C/T]TGACCTGAGCTGGGC | 93664 |
rs187573420 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122639794 | ATGTGGTCCCTTGAG[A/C]GCTCATAAACATTGG | 93664 |
rs187578586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122472174 | GCAGGCAGTTGATGC[A/G]GCTAAAACTGGAGGA | 93664 |
rs187591598 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122781062 | TTTCTTACCACACTC[A/G]TGATTATTAATTAAT | 93664 |
rs187591733 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122740323 | CAAAATTCAGTAGAT[C/G]AATGGATAAACTCGG | 93664 |
rs187593299 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | CADPS2 | GRCh38.p7 | 7:122721416 | CTACAAACACCTCTA[C/T]GCAAATAAACTAGAA | 93664 |
rs187610224 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122753187 | AAATCTAGTAGGGTA[A/T]AATTAAGTCAAAGAT | 93664 |
rs187649695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122633721 | CTCTGGCTGGGCTTC[C/T]AGTACTACGTTGAAC | 93664 |
rs187650460 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122643673 | GGTGAAAATTTCTGA[A/G]GGGGCAGAGGGAAGA | 93664 |
rs187651479 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122824343 | GCTTTTAACCATTAC[C/T]GCCAACACAACTCTC | 93664 |
rs187654532 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122835447 | GAGAATGACTTTGAC[A/C/G]AGTTGAGAGAAGAAG | 93664 |
rs187657645 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122386125 | CATGAATCTTTGGAC[G/T]ATTGCTATGTTATTG | 93664 |
rs187660288 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122851223 | GTGATGTCTACAGAA[A/G]GAAAGAGGGAAGATA | 93664 |
rs187661584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122872737 | AATATGTTAAACTAG[C/T]AAGAATACAAGTTTC | 93664 |
rs187664043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122721538 | GCTCTGAAATTGAGG[C/T]AATAATTAATAGCCT | 93664 |
rs187664557 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122693189 | TTATAAAAATACTGT[A/T]AACACTGTTCTCTCC | 93664 |
rs187666539 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122365610 | GTATATAAACACTTA[C/T]GGGTTTGCCTTTGTG | 93664 |
rs187667058 | snp | A/G | 0.00142988 | 0.0267001 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122702036 | GAACTCGCAGTTGAA[A/G]CTGGTCAATAGCTTT | 93664 |
rs187672676 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122665400 | TTCGGCTGACAGACT[A/T]CCGTACTGAAACACT | 93664 |
rs187673914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122808487 | AGTTTCATTACCTTC[C/T]GCTGGAGTGATAAAA | 93664 |
rs187675901 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122345802 | CAAGGAGCTTAAAAC[G/T]AAACCAAAAGTGAGC | 93664 |
rs187678992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122321102 | AAATCCAACAATATT[C/T]TTCTGTGGCACTTAA | 93664 |
rs187679985 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122673645 | GATTGGTGCAGCCAT[A/G]AATCCCGAGCTAGAC | 93664 |
rs187690178 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122468490 | GCATGAGGTACAGTC[C/T]TAACTACATACTTTT | 93664 |
rs187695876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122852641 | GAATGAAGGCAAAGG[C/T]AGGAACATGCTGGCA | 93664 |
rs187699680 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | CADPS2 | GRCh38.p7 | 7:122334785 | AGAGTACTTCCATTT[A/T]AAAAAAAATCTGTGG | 93664 |
rs187702564 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122424982 | GTAATAGCTTTTTTT[A/T]AAAAAATTATTTTTT | 93664 |
rs187717854 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122490531 | CATGACAGAGTATCA[C/T]TCTACAAGACATATA | 93664 |
rs187718955 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122429901 | TTTTTTAATAAACAC[A/G]TGGCCTCTAGACACA | 93664 |
rs187720314 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122730043 | TGGAGGTAAGAAACT[A/T]ACAAAAAATTAATGC | 93664 |
rs187723282 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122711108 | TAAGAATTACATTGA[A/C]AACAGTTGTCCAGAA | 93664 |
rs187727078 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122390201 | TTAAATCTCTTCACC[C/G]TAATATTCAGTGCCT | 93664 |
rs187734977 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122385383 | GCTAATGTCTATACC[G/T]GGGGCAATAGGTATA | 93664 |
rs187736981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122578905 | TCACAGAAGTTGCAA[A/G]TGGATCTGGTGCTAG | 93664 |
rs187737334 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122683929 | GGGGTGTGTGTGAGC[A/G]TGCCCTGTGATGAGA | 93664 |
rs187739223 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122787094 | TATTATCTAGAGAAG[C/T]CACTCCAGAAGGAAT | 93664 |
rs187740460 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122766304 | ATGAGTTTTGGAGAG[C/G]ACAAATCACATCCAA | 93664 |
rs187740980 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122345310 | CTTTTATTTTTTCTT[G/T]TATTTTTAGTAGAGA | 93664 |
rs187743996 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122748628 | CAGAAATGTCTGAAG[C/T]TTTTGCTTTCTTTCT | 93664 |
rs187749077 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122747996 | CACTTGCTTATGTGG[A/C]CTTTTCCTTACTAGG | 93664 |
rs187755097 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122785629 | CTCCCTGCCCTCCTC[C/T]TGGGCTCAAGGACAT | 93664 |
rs187755172 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122724931 | CGATTACAGAGAAAA[G/T]CAATTATAATGAAAT | 93664 |
rs187756532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122596583 | AGCTTCACGATGACC[C/T]TCATTTTAAGACAGA | 93664 |
rs187761165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122352383 | GTTTAGATGGACTGG[A/G]ATGGGTTTACTCAGC | 93664 |
rs187765833 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122856241 | CATGCTTTCTGTTCA[C/G]AGCCAACATAAGCCT | 93664 |
rs187775016 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122540575 | ACTTTAATTAGTAAT[C/G]TATCTCCTGGCAATT | 93664 |
rs187778675 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122520664 | AACTCGCTTACCCAA[A/G]CACTTTAAAAGCACT | 93664 |
rs187790779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122635008 | ATTGCCCTGTCGTCC[A/G]AAAGGATGCTTGGTA | 93664 |
rs187795159 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122558246 | AATAGGACTCAGTTC[A/C]TGTTTAGAGATTGTG | 93664 |
rs187795935 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122562213 | TTTTACCTTAAATGG[C/T]AAAGGAGAATTAAGG | 93664 |
rs187823228 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122525286 | GCAGAGCTCTGAAAT[A/T]TAGTAAACAAACTAT | 93664 |
rs187826744 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122666637 | ATGAGTCACCACGCC[C/T]AGCCAGCTAACACAA | 93664 |
rs187845184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122562976 | AAGTTCAAGTTCCAC[A/G]CAACCTAACGATTAA | 93664 |
rs187855474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122452761 | TATCATTCCAATGTA[C/T]TAATTTTAATGGTTA | 93664 |
rs187856060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122600153 | TCATCCAGGCCGTCA[A/G]AAGCTACATGATGGA | 93664 |
rs187856840 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2, RNF148 | GRCh38.p7 | 7:122701355 | ACAAAAAACCAAACA[C/T]CGCATGTTCTCACTC | 93664 |
rs187863094 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122487104 | CAACCTCCACCCCTC[A/G]GGTTCAAGCAGTTCT | 93664 |
rs187869700 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122687457 | CATGAGCTGTGGAAC[C/T]AGAACAAGTTCAAAT | 93664 |
rs187886605 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122381618 | AAGAGGTCATTGATA[A/C]CCATTTTCTTGAAAA | 93664 |
rs187895454 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122743859 | CATGTTTTTGAAATA[A/G]CAATGCATCCCAAGC | 93664 |
rs187896888 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122714858 | CTCTGTCTTATCTCA[C/T]TTAAAATTCACAACA | 93664 |
rs187897277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122783306 | GTTTGTATTTAATAT[A/G]ATAACTATTGTGGTT | 93664 |
rs187898969 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122726608 | CAGAGGATTAGCAAA[C/T]GACATGCACGAAACT | 93664 |
rs187901508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122813471 | TTTCAAATTGTTTAT[C/T]ACCATCAACGGAGTG | 93664 |
rs187903727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122341421 | GAAGAGTTTCAGAAA[C/T]CATCTGGAGTTCCAG | 93664 |
rs187905687 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122845581 | TTTCTCCATTCTCCT[C/T]GCTACATCCCCTCAG | 93664 |
rs187922483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122496560 | CATATTAGCCTCATC[C/T]CACAAGTAGCATTTT | 93664 |
rs187928236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122524309 | ACAAATATGTTAGGC[C/T]TTCATTTCCTTTTTT | 93664 |
rs187929910 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122478718 | AATGATGTGAGGACT[A/T]TCAGTGAGGGGCTTT | 93664 |
rs187933173 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122673191 | TGAACAGCAGCAAGA[C/T]TCATTGCAAAGAGCG | 93664 |
rs187937916 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122544164 | ATGAAATAGCAAGAA[G/T]CTTGAATGATTCAAA | 93664 |
rs187939294 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122561775 | CTGATCACTACAGTC[A/G]AGCTAATTAACATAT | 93664 |
rs187942175 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122657532 | TCCTTCACATCCCTT[A/G]TAAGTTGGATTCCTA | 93664 |
rs187944925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122626678 | AGCTCCACCAGGGCC[C/T]GGCAGAAATATTTTT | 93664 |
rs187947725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122873241 | AATGTGCAGGTTACA[C/T]AGGCATACACATGCC | 93664 |
rs187948955 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122688571 | TCCGCTCTGTCTCAG[C/T]TGTTTGAGCTGGCAG | 93664 |
rs187949511 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122463799 | CCAAAACTGCTTTGC[A/G]TGAAGTTCAGGGGTT | 93664 |
rs187951292 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122734321 | GGTATATTCAAAATG[A/G]CAACTGTGAAATAAC | 93664 |
rs187955314 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122706254 | ATATGCTTATATATT[C/G]AAGGAATATATATAT | 93664 |
rs187960347 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122426424 | TCATGGATATTTTAA[A/G]GGGCTCCTCTTTGAA | 93664 |
rs187962065 | snp | A/C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122504936 | TTTGGTGGAAGAATA[A/C/T]GTAAATTTATAAGAA | 93664 |
rs187968300 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122443978 | ACTCATGGCCTGCAA[A/G]TCTTCCCCCCAGATC | 93664 |
rs187970431 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122404842 | AAAAATATCTTACAT[A/C]TGGCCGGGCGCGGTG | 93664 |
rs187983171 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122521562 | GGGCATTAAGAAACT[G/T]AGAAGTAAATACTTT | 93664 |
rs187986996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122367990 | ATCTTTCTCTCTGAC[C/T]CTTTTCTTTTGCCAT | 93664 |
rs187988997 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122386672 | GTGTGTCTTACTTTT[A/G]TAGATGCAAACTCTG | 93664 |
rs187991630 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122474798 | AATCTTATTTTCCAA[C/G]TCTGAGAAAAGCTGT | 93664 |
rs187996053 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122588828 | TATTTGGTGAGAAGG[C/T]AGATGGGCACCTCCC | 93664 |
rs187997326 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122448801 | TAGGATCTTCTAAGG[A/C]AACTTTTTATGATCT | 93664 |
rs188007693 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CADPS2 | GRCh38.p7 | 7:122410359 | AAAAAAAACAAAAAA[C/T]AAAAACAAAAACAAA | 93664 |
rs188011500 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122739309 | GATAAATAAAATACA[C/T]ACTCTTCAAAAACTA | 93664 |
rs188018774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122692565 | CCACCCAGGCAGCAC[C/T]GCTGCCACTGGGTAC | 93664 |
rs188019213 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122711813 | ACGTGCCACCACACC[C/T]GGCTAATTTTTGTAT | 93664 |
rs188023286 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122677591 | TAGGGACTTCATGTA[C/T]ATTAACCCTCACAAC | 93664 |
rs188025290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122725362 | ATGTATAGGTATATA[C/T]GCATATGCGTGTGTG | 93664 |
rs188030365 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122372659 | GAAATATCTGGGATA[C/T]GAGAAATTCACTGTT | 93664 |
rs188044791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122758999 | GGATTTTCTTATTTC[A/G]GGAAAAAAAAAAAAA | 93664 |
rs188046663 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122800833 | CTGTCTCTACTAAAA[A/T]TACAAAAATTAGCCG | 93664 |
rs188052227 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122876708 | AAGAATATAATCTAA[A/G]ATAAGACTTATAGCT | 93664 |
rs188053086 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122779467 | ATATCATACCCACAG[A/T]CATTTCATTGGATAA | 93664 |
rs188060479 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122421870 | ATGGAGTTTTTCAGA[A/T]TGAAATTATTGTGGT | 93664 |
rs188090895 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122358945 | GATGAAGAGTCTGGA[A/T]ATGATTGCCATAGAA | 93664 |
rs188098052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122618175 | TTAGCGTTTTGTGGA[C/T]TGGCTCATCTCTTGC | 93664 |
rs188105211 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122338319 | GAATTGCTTGAGCCC[A/C/G]GGAGGCAGAGGTTAC | 93664 |
rs188110904 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122650255 | AATATATATCAAATA[A/T]ATAATTTTAAATTTG | 93664 |
rs188112291 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122731173 | AACCAAAGTAGAACA[C/T]AAACAAATGAAAACA | 93664 |
rs188118563 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122704763 | CAATCATCTATCTCT[C/T]AAAAAGTGGTTTTCA | 93664 |
rs188126064 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122586023 | TAAACACTTAAGCAA[A/G/T]ATAAATATAAAATAT | 93664 |
rs188135337 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122862398 | TAATCCAAGGAAAGA[A/G]GAGAAAGAAGACAGG | 93664 |
rs188152625 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122683027 | GCCCTGGAGCAGCTC[C/T]CAGCCCCTGTCCTCT | 93664 |
rs188156293 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122559640 | GTCAGGCATGGTGGC[A/G]GGTGCCTGTAATCCC | 93664 |
rs188162400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122620874 | CTATTTCTACCCACG[C/T]GCGTTTTGATGCTTA | 93664 |
rs188165285 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122707134 | CCTGAAGTATCCCCA[A/G]AGGAATAATACTTAA | 93664 |
rs188165669 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122762844 | ACTTCATCACCCTAC[C/T]TTCCTTTCAATGATG | 93664 |
rs188170605 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122654444 | ATGAAGCTGGTGAGT[C/T]TAGGTTGAAGCTAAT | 93664 |
rs188173754 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122361592 | AATCTAGTCACTATA[C/T]ATATGAGACCACTGA | 93664 |
rs188175355 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122695570 | AAACAGCTATGTAAA[C/G]TGCTTAGTCCTCTAC | 93664 |
rs188177364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122876091 | TTTGGGAGGCTGAGG[C/T]GGGTGGATCACTTGA | 93664 |
rs188179007 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122681293 | TAATAAAAGAAAGAG[C/T]TCTCCGGTCCGTGCC | 93664 |
rs188180169 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122831967 | TCCTGGTTATATGAA[G/T]GCAACATAAATTATG | 93664 |
rs188196053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122401251 | AGAGATGCTGTGACA[C/T]TGATTATATAAGCAC | 93664 |
rs188196272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122805229 | CAGTGGCACTATCTC[A/G]GCTCACTGCAACCTC | 93664 |
rs188206177 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122865385 | GACTGAACTTAAGTC[A/T]TGGCTATAGCTGCAA | 93664 |
rs188216085 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122535776 | ATGATATACTGAGCC[C/G]CACATCAGTGAAAGT | 93664 |
rs188221529 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122372469 | ACTGTTTAGTACTGT[G/T]TGTGATTGAGAACTT | 93664 |
rs188221749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122517478 | ACAAGAAACTGCCAA[A/G]TTGTTTTCCAAACTG | 93664 |
rs188230667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122667700 | ATTAACTCTGCTGGG[A/G]GGCCAGAGTAAGAGA | 93664 |
rs188235939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122761252 | AATTAAGTGAACGTT[C/T]CCATACACAATGTTA | 93664 |
rs188239631 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122327899 | CAATAAATTGTTCTA[A/T]CAGCAAAAGCTTCTA | 93664 |
rs188240295 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | CADPS2 | GRCh38.p7 | 7:122885704 | CTAATCCGGCCAGAG[C/G]TGCGCCTGCCGGGTG | 93664 |
rs188240408 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122454349 | TTCCCAAGGTCACAC[C/T]GCTGGGAAATGCAGG | 93664 |
rs188240959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122651826 | TTTAAGAGACAAATA[C/T]AGAAGTTAAAGGAAA | 93664 |
rs188241863 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122804856 | CCTCATTTGTTTGCT[A/C]TTTCTAATACCATAT | 93664 |
rs188242164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122479164 | AGGACTAAAAGGGTG[C/T]TGCCAGCCAAGACTG | 93664 |
rs188246361 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122618933 | ATTATGCTATGGTAG[A/G]AAAATATCTGCCTTA | 93664 |
rs188246679 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122734760 | TGTTGCATACCAAGT[A/G]TGTATTACCTGGAAA | 93664 |
rs188250077 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122636554 | CACTGCAATCTCCGC[A/G]TCCCAGGTTCAAGCA | 93664 |
rs188252506 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122474233 | AATCCTTTATCCCTC[A/T]CTCTCACTACCCTTA | 93664 |
rs188254405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122435880 | AGTCACAGTACATAA[C/T]AACACATGATACCAC | 93664 |
rs188256890 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122497227 | TTATATTTTAGATCT[A/C]TATGAACAACAACTG | 93664 |
rs188268745 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122397906 | TCAAAAAGTGATTAC[C/T]GCCTGAGGGGAAAGC | 93664 |
rs188268919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122418452 | AGATAATAAGTAGAC[C/T]AGATGACTATATCCT | 93664 |
rs188272271 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122568489 | AATACCTAATAGCTA[C/T]ATAATATAATATTTA | 93664 |
rs188284746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122378914 | ATTTTGAGCATCAAA[C/T]TGGAAATCCTGGGAA | 93664 |
rs188303044 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | CADPS2 | GRCh38.p7 | 7:122502290 | AAATTTCACTAACTA[G/T]GTCTGAAATTAATAT | 93664 |
rs188318010 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122611873 | ATATTATGATAGTGG[C/G]AATTGTGCAAGGAAT | 93664 |
rs188327911 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122540052 | CTCATTTCAAGTACA[C/T]GTCATTTTCAGTTAA | 93664 |
rs188332880 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122369131 | GAATTTTTGTTTCCC[C/G]CCCCCCCCCCCTTTT | 93664 |
rs188348820 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122512022 | AATCTGTGTGTGCAC[A/G]TGTATGTATCTTTTA | 93664 |
rs188350620 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122577509 | AGCTTGTTTCTATTA[C/T]TGAATAGTATTCCAT | 93664 |
rs188350964 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122400195 | AATCCCAGCACTTTG[C/G]GAGGCCGAGGCGGGT | 93664 |
rs188369921 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122475415 | CTCCATTGTTCCCTA[A/C]AATTCACAGATAGAT | 93664 |
rs188370154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122437680 | CTGTTACTTTTAATT[A/G]CATAAATTAATGTGT | 93664 |
rs188383840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122757223 | ATAATCATGGCTCAC[C/T]ACAGCTTCTACCTAC | 93664 |
rs188386882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122459477 | TTATCAGCTTACACT[C/T]TGGCCTGCAGTGCAT | 93664 |
rs188392482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122719470 | GGCATGTGCAATGAC[A/G]CCAATTTGAAAAACA | 93664 |
rs188395038 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122837977 | CAGAGACACAACAAA[A/G]AAAGAGAATTTTAGA | 93664 |
rs188397385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122858136 | ATTTTACAGAGTGCC[A/G]ATTGGTCCATTTTAC | 93664 |
rs188401140 | snp | C/G | 0.00365642 | 0.0426009 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122438420 | TCTGACCACTTTCTT[C/G]ACCTCTTCTGCTGGT | 93664 |
rs188409197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122401695 | TACCATTTAAACTGA[C/T]TGCCCATTAAATTAC | 93664 |
rs188415435 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122423139 | TGGAAAGTCTAAATT[C/T]TTATCTAGATTTTCT | 93664 |
rs188415575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122353984 | TTTCCCTCTTTCTAG[A/G]AACAGTCAGATTTCT | 93664 |
rs188419124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122382292 | AATTGAAATATGTCA[A/G]TAAATGTAATTAATG | 93664 |
rs188419712 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122638867 | ATCCTGAATCCTGAC[A/G]TGGTTTCTTAGATGA | 93664 |
rs188433553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122362850 | GCTGATCAATTACTA[C/T]AAAATAGTTTATGCA | 93664 |
rs188436092 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122669664 | CCACAATCATAAGGC[A/G]GCTACATTTCCCCTG | 93664 |
rs188439805 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122604394 | TTTGTACTTTAATGC[C/T]CCCTTAGGAACCCTG | 93664 |
rs188447135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122764051 | TGCTCGAGCTTTTTG[A/G]TCCCCTAGGCACCTC | 93664 |
rs188452345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122330881 | GGATTGAGTCTGTTA[C/T]GCACCTTCTCTATGC | 93664 |
rs188452356 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122736007 | GTCCAGTTGGACATA[A/C]CCACTCTTGACATTA | 93664 |
rs188453558 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | CADPS2 | GRCh38.p7 | 7:122745575 | CCATTAGAACAAAAG[C/T]GGCTTTAGGATAAGA | 93664 |
rs188455395 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | CADPS2 | GRCh38.p7 | 7:122669279 | GAGGTTGTAGTGAGC[C/T]ATGATCACACCACTG | 93664 |
rs188463742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122784557 | CAAGTCCTTTTCTTA[A/G]TCTAGGCAGGAAAAT | 93664 |
rs188464601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122707968 | TATTTTAAGTAAATT[C/T]TGTTGTGTATATTTA | 93664 |
rs188471752 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122722933 | AAGCAATGGGTAAAC[A/G]ATTCCCTATTTAATA | 93664 |
rs188472384 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122822404 | TCTCTCCCACTCTAG[G/T]TTCCCACACCGCCCC | 93664 |
rs188472847 | snp | C/T | 0.000115415 | 0.00759568 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698072 | AAATCCAGGGGTCAA[C/T]GCAATTCTTGTGGAA | 93664 |
rs188473419 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122422144 | AAAAAGGGAGAAAAT[A/G]GGAAAATATCTACTA | 93664 |
rs188474070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122776428 | TAGGTGATTTCTTCA[C/T]AGTGGTATGAAAATG | 93664 |
rs188476294 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122806216 | CTAAATGTTTCCTTA[C/T]ATCTCTGAGGATGTG | 93664 |
rs188479139 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122496062 | CTTTTTAATGTTTTC[A/G]AGAAATGTTATTGCA | 93664 |
rs188486189 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | CADPS2 | GRCh38.p7 | 7:122754637 | GCCCACCATCACGCC[A/C]GGCGAATTTTTGTAT | 93664 |
rs188488069 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122796576 | CACACCTACAACTAT[C/T]AGATCTTCAACAAAC | 93664 |
rs188488444 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122627154 | CTGCCTCAGCCACTT[A/G]TTTGTTATGTAATCA | 93664 |
rs188493799 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122533702 | AAAAAAGCAATTGAC[A/C]TAAGTAGAAGAGCTA | 93664 |
rs188503729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122463231 | AACAAGTGATAAAGA[A/G]TTGGTATCACACAGA | 93664 |
rs188513294 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122644692 | GTCCTTTTTCTTAAT[A/C]ATTGAGAATTAGCTA | 93664 |
rs188513893 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122351919 | ATGTTACATTTTATT[A/G]TATCAATGGGGAAAA | 93664 |
rs188515060 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | CADPS2, LOC105375481 | GRCh38.p7 | 7:122529649 | ATATTTTTCCTCCCT[G/T]TCTTTTGGATGGCAC | 93664 |
rs188515229 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122574824 | TCTTTAGCTAAAACA[A/C]TGAGTGAAAGGTGGT | 93664 |
rs188515641 | snp | A/G/T | 0.00199529 | 0.0315338 | intron-variant | CADPS2 | GRCh38.p7 | 7:122782596 | ACCCTGGGTGACAGA[A/G/T]TGAGACCCTGTCTCA | 93664 |
rs188517363 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122594016 | AAATTTTAATAGAAG[A/T]ACTAGACAATACCTT | 93664 |
rs188517555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122753832 | TCACCCACTGGGGTG[C/T]TGCATATTTCACAGA | 93664 |
rs188523038 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122696347 | GCAGTTCTTTCAAAG[A/T]AGAGCTCTTGTGATT | 93664 |
rs188523516 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122547169 | GGTATACTCTACCCA[C/T]AAGAAATGTTGCTAA | 93664 |
rs188529402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122609208 | CTTGGAGGGAATAAA[A/G]GACTAGTACATATAA | 93664 |
rs188531983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122425660 | ATGTGTATATACACA[C/T]ATACACATTCAGTAG | 93664 |
rs188538030 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122788040 | AGAGCACACTATGGG[A/G]GACTGAGAAAGTAGA | 93664 |
rs188538217 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122825874 | CACGTCCCCTCCAGG[C/T]CAGCCAAGGTCAAGT | 93664 |
rs188544994 | snp | C/T | 0.311614 | 0.242289 | intron-variant | CADPS2 | GRCh38.p7 | 7:122819667 | AGTTATCCCCACCTG[C/T]CCAGTTCCCTTATTA | 93664 |
rs188556852 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122861099 | GACATATGAATTTCA[C/T]TTCCTTTGAATAGAT | 93664 |
rs188558884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122855443 | CAAACACAAATAAAG[C/T]GTCCTTCCATTCACA | 93664 |
rs188577257 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122661077 | AGACAATGTAGATTT[C/T]AGAAAAAGGAAAATA | 93664 |
rs188577692 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122635357 | CTATGTATACATGTG[A/C]CATGCTGGTGTGCTG | 93664 |
rs188592516 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122596495 | GAAGGCAAACAGACT[C/T]TGGCCTTCGTGACTC | 93664 |
rs188595673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122430057 | TTCTCCTCTCAAAGA[C/T]AGTAGGCAGTCTGGG | 93664 |
rs188597782 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122630587 | TAGTTCCTACAACAA[C/T]GGGACTTCCTTGAGA | 93664 |
rs188609748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122411453 | TTGAACTCCTGACTT[C/T]AGGTAATCCACCCGC | 93664 |
rs188610396 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122691348 | GGAGCTCAGCTCCCT[C/T]CCACAGCTAGGACTA | 93664 |
rs188612392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122605887 | GCATTAATTTTAATC[C/T]AGGATTTTTTTTTCT | 93664 |
rs188626159 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122373521 | TCACGCCTGCCCAAA[A/G]GCCCTAACAGCTGGC | 93664 |
rs188626881 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122557754 | GTGAACTATGGCACA[C/G]CGGCTGGCTATTTGC | 93664 |
rs188628255 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122391115 | TGTTTCTTTTTATTA[A/C]TGTTTCAAACTTCAA | 93664 |
rs188643728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122352963 | TAATGCATGGGAGCC[A/G]GAAGCATCATTCCAG | 93664 |
rs188643784 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122632844 | GTCTTACATTTAAGT[C/T]GTTAATCCACCCTGA | 93664 |
rs188650080 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122658986 | ACAGCTCAACTCCTA[C/G]TCAGATTAACATAAA | 93664 |
rs188660169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122458482 | AATTAATTGTGTCTT[C/T]ATATGATCATTGAGA | 93664 |
rs188678539 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122880319 | TAAAAGACAGTACTG[G/T]GAATATAATTTAAAA | 93664 |
rs188679221 | snp | A/C/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122778857 | AAACTTGGGAGGGAC[A/C/G]AGGGGTGGAATGATA | 93664 |
rs188680257 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122664125 | TATGAACCCAACATC[C/T]ATACCTGTGTCTGAG | 93664 |
rs188684277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122738275 | TTAACAATTTCAAGA[C/T]GGCAGGAACAGAGAG | 93664 |
rs188684897 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | CADPS2 | GRCh38.p7 | 7:122476801 | TATTTTTAAAACACA[A/G]GCTGTGAAGACCAAA | 93664 |
rs188685706 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122616093 | ATCATTCTTATTGGA[C/T]GTATGTATCAAATAT | 93664 |
rs188686006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122648415 | ACCTGCAATCTCGAC[A/G]TGGACAATCAATATT | 93664 |
rs188687440 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122346094 | AAAATGCGCTGAGTG[C/T]CATGGCTCATGCCTG | 93664 |
rs188693331 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122376628 | GTTATGCATGATGAA[A/T]AAGTCCTGGAGAGCT | 93664 |
rs188694924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122513848 | CTGATTTCTAAGGTC[C/T]CTGCTAGCTCCATCA | 93664 |
rs188700789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122494151 | AACTAAGGTTTTCTG[A/G]AAAAGAAGACATTTT | 93664 |
rs188708093 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817724 | GGCAAGTACCCCTCA[A/T]CCCCTTCTCCTTCAC | 93664 |
rs188710781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122459929 | TTTAAGAAGGGCAAA[A/G]GTATAAACATCTGAT | 93664 |
rs188713823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122852038 | CAAACAGCTAGTAAG[C/T]GGCAGAACTGTAATT | 93664 |
rs188736099 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122710941 | TAGCACAATAAAACT[G/T]GCTCAAGGTCCCTGA | 93664 |
rs188748990 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122718985 | TGATAATAAAACTTT[A/T]AGGACTGACATCCTA | 93664 |
rs188751473 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122738652 | ATGACTTGGCTCAAA[A/G]AGAAGGCTGATGTGA | 93664 |
rs188754280 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122683505 | AAATACTTTTTGTTT[C/T]GTAACAATTTTATAT | 93664 |
rs188755676 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122838308 | GCTATTTATGACAAA[C/T]CCACAGCCAATATTA | 93664 |
rs188757176 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122797496 | ATGTGGTACATATAC[C/T]CCATGGAACAGTATG | 93664 |
rs188769801 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122816886 | AGAAGTGTAAATGGC[C/T]GATCCTTGCCTTAAA | 93664 |
rs188773444 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122858687 | TAATATTTGAAACAC[A/G]TTATATATAGTTGAC | 93664 |
rs188790536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122834682 | CCCACGGAGCCTTGC[C/T]CACTGCTAGCACAGC | 93664 |
rs188794121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554041 | CATTTCTTCCCCAGG[C/T]AACAGTAGCAGTTTT | 93664 |
rs188799474 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122442969 | CAAATTAGCAAAGTA[A/C]CTTTAATCATTTTGT | 93664 |
rs188811786 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122404326 | AAGGACATGAACTCA[C/T]CATTTTTTAAGGCTG | 93664 |
rs188813297 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122516979 | TTGACACAGTCATGT[A/T]ACCACCACCACAATC | 93664 |
rs188813390 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122809555 | ATTGCACTCCAGCCT[A/G]GGCAATAGAGAGAGA | 93664 |
rs188841826 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | CADPS2 | GRCh38.p7 | 7:122839714 | TCAGAGAAATGCAAA[A/T]CAAAACCACAATGAG | 93664 |
rs188849070 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122532213 | CCTTTTTGAGGAGGA[A/G]ATAAAAATGACCATT | 93664 |
rs188849475 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122484980 | TTAGTAGATCTATCA[C/T]GGTCATCTGTGGAAA | 93664 |
rs188855493 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122882705 | AATTAGTACCTGATT[C/T]GTATTATTGTTTTTC | 93664 |
rs188858253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122451132 | AAATGCAAAAGGCAA[A/G]TAAGAGGTGCAGTGG | 93664 |
rs188864532 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122551767 | TCCATCTGTTAATTA[C/T]TGATTATAGGAGAAA | 93664 |
rs188866325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122646602 | AGGAACAGCGAGTAA[C/T]TCACTTTATCTAGAA | 93664 |
rs188868588 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122415073 | TCTCAGAATGAGCAG[C/T]TTGCTTGGTGAAAAG | 93664 |
rs188869367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122570937 | TACCTAATGCTAAGT[A/G]ACGAGTTAATGGGTG | 93664 |
rs188871669 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122522549 | CACCTCAAACATTTA[A/T]TTCTTTGTAGTGGGA | 93664 |
rs188873770 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122502968 | TTCAGCCATAACACT[G/T]ATTTCATAAGAATAT | 93664 |
rs188879408 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122680531 | CCAGCCTGGCCAACA[A/T]GGCAAAAGCCTGTCT | 93664 |
rs188887592 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122704403 | GGCTGATTCTATTAA[C/T]AGTGACAAATTGAAG | 93664 |
rs188890836 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122469272 | CACCTTAGGTTCCCA[A/G]TTTAATTTTACCTTT | 93664 |
rs188894081 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122675994 | AAAGTAAAAAAAACA[A/G]CAACAAAAAAAGAAA | 93664 |
rs188894964 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122849056 | TGATTCTAAAGTTTC[C/T]ATTTGAAGACTAAGG | 93664 |
rs188900894 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122871129 | TGAAAATGGAAAAGT[C/G]AAACAAAGGAAGACA | 93664 |
rs188901923 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122622361 | AGCAAAAGGAAATTT[A/G]TGATAAAAACTATTA | 93664 |
rs188902534 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122706681 | GTAGAACATACATAT[A/G]TATATTCTTTTATAT | 93664 |
rs188903263 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122449419 | TTCCCAGGCTCAAGT[A/G]ATCCTCCCACATCAG | 93664 |
rs188909713 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122362620 | CTCTCCTCCTTAGAA[C/T]TAAAATAATATGAAC | 93664 |
rs188922311 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122430685 | GGTAGCATTTTATAA[C/T]CCCAAGATTAAAAAC | 93664 |
rs188926874 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122612406 | CTAATAACTTGAATG[A/T]TTTAAAGATAAAATT | 93664 |
rs188928614 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122716459 | CAGCCTAAAAGAGCA[C/G]GGGTAAGGGAGCTCC | 93664 |
rs188931665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122412499 | ACATATGCACAAATA[C/T]GTGTGTTCACACTGA | 93664 |
rs188934489 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122728685 | ACATTCAGACACTTG[G/T]GCAACTGGAGGGAGC | 93664 |
rs188936781 | snp | A/T | | | intron-variant, utr-variant-5-prime | CADPS2, RNF148 | GRCh38.p7 | 7:122702868 | CATAAATGGAAAAGG[A/T]CTCCCTGGATCAAAG | 93664 |
rs188953187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122593074 | CACAGAGTTTAATAA[C/T]ATACTGCATGCAATA | 93664 |
rs188966083 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122394827 | CATGATATGATCTCT[C/G/T]TGGCTGCTGTGTGGA | 93664 |
rs188967120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122744792 | AATGACGCCTACCCA[C/T]ATTCTCATTGATCTC | 93664 |
rs188969556 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122763302 | CTATGAAACTAAGGG[A/G]TTCCTCCCCAGAAAG | 93664 |
rs188970709 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122626192 | TTTTCTTTTTTTCTC[A/C]GCAACATAGGGAATC | 93664 |
rs188973849 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122321769 | ACAGGCGTGAGCCAC[A/T]GCACTCAGCCATGTT | 93664 |
rs188975885 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122799737 | GATTAAAATGTTAAC[A/C]CTGGCACTCATATTA | 93664 |
rs188976187 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122355649 | CTTCTTATCCAGAAA[A/T]TTTTTTCTAGCTCTT | 93664 |
rs188981002 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122405641 | CTCCAGCCTGGGCGA[C/T]GGAACAAGCTCTGTC | 93664 |
rs188981805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122835797 | AAAGACCAAACCTAT[A/G]TCTGATTGGTGCACC | 93664 |
rs188983090 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122769478 | ACCTACATCCCCAAC[A/T]CTTCACCTCATAACA | 93664 |
rs188987323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122810629 | ATATAACCATTTATT[C/T]GCAGGATTTTATCTA | 93664 |
rs188997164 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122552443 | ATATCCTCTTTAGTC[C/T]TTTCCTTCACCTTTA | 93664 |
rs188997598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122368711 | AAACTATAAAAATGT[C/T]TGAAAAGTCCCTAGT | 93664 |
rs189010683 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122322696 | AAGGTAAAAACTTTG[A/C]AAATAATTTCAGTCT | 93664 |
rs189038084 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122852933 | CTGCAGAATCCTACA[G/T]GCAGACTGCTTTGCA | 93664 |
rs189043432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122758537 | CTGTATTCAAAATAC[C/T]ATACCTTTAAAAAAT | 93664 |
rs189044096 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122874092 | AGATTGCAAAATTTT[C/T]CTCCCATTCTGTAGG | 93664 |
rs189052235 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122406014 | AGTAAGTGACAGAGA[C/G]ACGTGAATCTGTCTA | 93664 |
rs189065951 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122535530 | TAATAAATATGTTTT[A/G]TTTTTATAAAGTCTG | 93664 |
rs189070876 | snp | A/G | 0.000399281 | 0.0141238 | missense | CADPS2 | GRCh38.p7 | 7:122387057 | AGGGCACAGAGTTTG[A/G]TGCTTTGCTTTTTGG | 93664 |
rs189071347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122733349 | AATACCCATTCACTC[A/G]GTCATCAAGTATTCA | 93664 |
rs189073449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122546794 | TCCATTCCTCTCCGT[A/G]TACAGTCTAGGACTC | 93664 |
rs189078580 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122573221 | CCAACTAAAGGAAAT[G/T]CTTGGACCTAGAAAC | 93664 |
rs189078777 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122347765 | TAGCAAGATTATACA[C/T]TGGCTCTTCCAGTGA | 93664 |
rs189081173 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122416756 | GGGAGGAAGGCAGAA[C/G]TGTTCTTTGAAGCTG | 93664 |
rs189085218 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122671560 | ACAGAGTAAGACCAT[C/T]GCTTAAAAAAAAAAC | 93664 |
rs189093084 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122324034 | AAGCCAATTATGAAC[C/T]TATCATATTGTCCTT | 93664 |
rs189112158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122471805 | GTAACTTGTGCCTCT[C/T]CAATGTCATTCAAAA | 93664 |
rs189113795 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122818069 | CAACCTCTTATCTCT[A/G]CACCCCAACCCCTTT | 93664 |
rs189121704 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122836249 | GATTTTGTCACCACC[A/T]GGCCTGCCCTAAAAG | 93664 |
rs189122664 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122507859 | GCTATGGAACAGCAA[C/T]CTTTTCTGCCATGAG | 93664 |
rs189126563 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122623918 | TTAGCACAAGAACAA[A/C]AATAATCTATTTGTA | 93664 |
rs189127301 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122791296 | GAAATACTAAGGAAA[C/G]CACGGATGGTATGAG | 93664 |
rs189133564 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122597616 | AATCTCTTATCATTT[G/T]TTTATTCTCTAAAAA | 93664 |
rs189143900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122613694 | TTTTTTTTTTCTTGA[A/G]ATGATGAGCATATTC | 93664 |
rs189146375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122571350 | AACATTTGTTCTACC[C/T]GAGACAGAGGAAAAC | 93664 |
rs189148113 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122656888 | AGTCCTTGCCCATGC[C/T]TATGTCCTGAATGGT | 93664 |
rs189149158 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122444589 | GAGCATCTTTCCATA[G/T]GCCTTTTTGTATAAT | 93664 |
rs189152273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122692140 | ATACTCGGGCAGGAC[C/T]AGGTTGTACACCAAC | 93664 |
rs189154783 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122434115 | AGGAATGTTGTAGGG[A/G]AGAAAATGCCTTAAG | 93664 |
rs189156689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122676810 | ATGGGACAAGATTCC[A/G]AACTCACTGTAAGTG | 93664 |
rs189158388 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122640701 | CTTTGGGAGGCCGAG[G/T]CAGGCGGATCACAAG | 93664 |
rs189161409 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122590583 | TGCTGCAACAGACAC[A/C]TTCATATATATTCAT | 93664 |
rs189162249 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122632555 | TTTGAGTTGGATTGA[C/T]TTTGCTTGATTTAAG | 93664 |
rs189163612 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122667383 | CTAGATTCCACCAAG[A/T]AACCAAATCACATTT | 93664 |
rs189164321 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122541904 | ATATATATTTATATA[G/T]TCATATATATTTATA | 93664 |
rs189164409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122560390 | TAACATTTAGTAAAA[C/T]AATGTTTACAAACCA | 93664 |
rs189165017 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122606479 | TCTGGAAGTGACCAT[A/G]GAACTAGGGCCTAAA | 93664 |
rs189171800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122579893 | CAAAATCTCTGGAGT[A/G]TAGATACAGACTTAC | 93664 |
rs189184115 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122674888 | TAATTTCCATAACCT[A/G]TGCTGTCCTTGGAGA | 93664 |
rs189185206 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122503548 | ATACTAATATGATTG[A/C]TCTTTCCTATGTTGT | 93664 |
rs189186822 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122741781 | CAAGTATAAAAATTG[A/T]AATCAGTGTCCCTAT | 93664 |
rs189190634 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122721974 | GATGCAGAAAAGGCC[A/G]TTAACAAAATTCAAC | 93664 |
rs189198276 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122645398 | ACATGTGTGTGTATA[C/T]ATGTACATATACACA | 93664 |
rs189202646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122522894 | CCATGTGGCTGCAAA[C/T]GACAGGATTTCATTC | 93664 |
rs189205693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122694980 | AAAACCCGTTAAATG[C/T]GGTGAAGGGGTTTAA | 93664 |
rs189206928 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122754040 | GGTAGGAGCTGTGCA[A/G]TGTTACACAAAACTG | 93664 |
rs189215473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122703116 | AAGATACATAACAAT[C/T]TGAATAGGCTGTAAA | 93664 |
rs189248513 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122607996 | GGGCGAGGTGGGTGG[A/G]TCACGAGGTCAAGAG | 93664 |
rs189249986 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122586787 | AGTATTTAATATATC[A/G]GGATCCTAAAGAATC | 93664 |
rs189260552 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122790702 | CCTCAGTCATTCTTC[A/T]AATTATAGCTCATGA | 93664 |
rs189262823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122386827 | CCACTAATGCAATTT[C/T]AGACCATATTTATAT | 93664 |
rs189282307 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122431483 | TTCAACACCTGACAT[C/T]GTGAGGAATGTGGGG | 93664 |
rs189283797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122346724 | TCTTCTAATAGTAGA[A/G]GAGGTAATACAATTT | 93664 |
rs189284473 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122392690 | AAAGAAGAACTTCCT[A/G]GTTTTGGCAATGAAA | 93664 |
rs189292113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122828020 | AATGCTTAAGTCCCT[A/G]CCAATAACTGTGGAT | 93664 |
rs189337954 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122445481 | TGATATTATTTAATT[C/T]CAATTTCTGATTGTT | 93664 |
rs189338141 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122528019 | ATATTAGCTCCCTTG[C/T]TATAATAGATGGGGT | 93664 |
rs189339386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122751914 | CAGATATAGGGCCAG[A/G]TCAAGTCCTTATTTA | 93664 |
rs189341102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122729057 | TGGTATTTATCATTC[A/G]TTTGCTACCTCCATG | 93664 |
rs189344269 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122465896 | TGTACGTCAACATAG[A/T]TCTACAAATATCAAA | 93664 |
rs189347566 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122796457 | TCACACTACCCAACT[C/T]CAAACTATACTACAG | 93664 |
rs189348722 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122720607 | ATACATACATATATA[C/T]GTATACATACATATA | 93664 |
rs189349675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122833678 | TGGGGTTACAGACAT[A/G]AGCCACCACGCCTGG | 93664 |
rs189353216 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122427826 | ACTAGAATTTTGATG[G/T]ATACTGCAATGAATT | 93664 |
rs189355783 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122475988 | TGAACTTCTTTTGCA[C/T]TTTATTCTTCTGAGT | 93664 |
rs189370872 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122751367 | GAGGGAATGGGTAAT[A/G]AAATAAGGGCCCCCT | 93664 |
rs189371162 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122564767 | TAGAATCAACCAAAA[A/T]GTCTATCAACAGATA | 93664 |
rs189372709 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122712943 | ACCTCCTAATACCAT[C/T]ACCTTGGGGGTCAAG | 93664 |
rs189374921 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122726048 | GACAGTAAATTTTAA[C/T]TCACCAGCTTAACCA | 93664 |
rs189382916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122768628 | TGTTTTCAATATTGT[A/G]GAGATATAAAATTCA | 93664 |
rs189383071 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122699935 | ACCATTAGCAGCAAT[A/C]AGTAGATGCTTTTAT | 93664 |
rs189385277 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122488309 | TGATGCCCAATGCAG[G/T]CACAGTCCAGGGATA | 93664 |
rs189385832 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122601231 | TTTTGAAGATTCTTA[C/T]GAGAATTTGCCAAAT | 93664 |
rs189396561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122789950 | TTAGAAAAACGAACT[A/G]TAAAGACAGAGTACT | 93664 |
rs189397952 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CADPS2, LOC105375481 | GRCh38.p7 | 7:122528534 | TTAGGGGAGAATGAA[A/T]AACTAAGTAAAGCCA | 93664 |
rs189410298 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122826727 | GGACAGGGGAAAAGA[C/T]CACTGAAATGGAAAA | 93664 |
rs189410555 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122740595 | AATTTCTGTACCATC[C/T]ACTCAAGCTCAATTT | 93664 |
rs189417169 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122810062 | TACCTTGCAGTAGAG[C/G]ACCTGATTAAATTTG | 93664 |
rs189440660 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122537014 | ACCACATACTGAGAC[C/T]TTTTTGAGGGTGGAG | 93664 |
rs189441307 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122685409 | ATTCTTCAAGCGTTT[A/G]ATGGCAGCTAACACT | 93664 |
rs189443528 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122464960 | AACATTAAGGGAAAC[A/G]GAAATACGAAAACTC | 93664 |
rs189453375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122427113 | TGAAGAAGACATTAC[A/G]TAAATGCCGTGTGTG | 93664 |
rs189458703 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122452507 | TTCAAGCAATTCTCC[C/T]GCCTCAGCCTCCTGA | 93664 |
rs189463069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122465844 | ATACCCAATCCTGAT[A/G]AAACCAGTATGAGAA | 93664 |
rs189464932 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122497889 | AGTAATTTTGAAGAT[A/T]TTCCATTGTCAGAAG | 93664 |
rs189470065 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122659787 | CCTTACCTCTAAAGA[A/G]TAAAGGATAAGAACT | 93664 |
rs189476086 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122600925 | TTTCAGAGGGAACAG[A/C]TAAAGTTATTTAACA | 93664 |
rs189483217 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122735424 | AGAAGAGAACATAAT[C/G]CTCATGTAGAACACA | 93664 |
rs189484275 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122618382 | ATATAACCTTCCTGC[A/G]ACTTATATTCTAGTA | 93664 |
rs189491217 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122717470 | TAAGACACTTACTTA[C/T]GACACAACTTACATA | 93664 |
rs189498362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122635574 | TGAGAATGATGATTT[C/T]CATTTTCATCTATGT | 93664 |
rs189500432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122518678 | CTACCTTCCTCATGA[C/T]TGTGTGATTAACTCA | 93664 |
rs189501572 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122689730 | AGCCTTGGTAAGGCC[A/G]CTTATTCCACAACAC | 93664 |
rs189502683 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122563222 | ACAGGAAAGCATCAC[C/T]ATTCTTGATCTATTG | 93664 |
rs189504663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122546013 | TTTAAATCATGAGAA[C/T]AAGATGTGCTTTTCT | 93664 |
rs189506352 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122498313 | ATTTTGCACTTTCAT[C/T]ATGAAATTTCTAGGA | 93664 |
rs189519412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122586179 | GAACGTGCACATTTT[A/G]TTCATTTAAAAAAAT | 93664 |
rs189524663 | snp | A/C | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122840637 | TGTAGCCAGGAGAGG[A/C]AGGCATGGTGGTATG | 93664 |
rs189524738 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122667838 | AAGAACAACAGCAAT[A/G]AAGCACAAAAGAATA | 93664 |
rs189530009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122861950 | ACCTGGAATTCTATG[C/T]GCAGCCAATTTCCCT | 93664 |
rs189531759 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122689237 | TCCTGGGACACCCCT[C/T]GTAAAGCTGCCATTA | 93664 |
rs189539215 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122637109 | TGTCTTTAAGCTCTG[A/C]AATTCCTTCCTCAGT | 93664 |
rs189542734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122601061 | CATTAGAATCATATT[C/T]ATAGTGCATAAATAT | 93664 |
rs189550051 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122358529 | AAAACTCATCACCAA[A/G]TCCAAGGCCATATAT | 93664 |
rs189555890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122337727 | AGCGGTAATTCGAGA[A/G]CAGAGGTTTTAAAGA | 93664 |
rs189561671 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122412788 | CTACTGATATTCTCC[A/G]CACTCCATCCATCCC | 93664 |
rs189567244 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122715464 | CTGACACAGGATTTC[C/T]GTGCCTTGTAATTTA | 93664 |
rs189576780 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122878879 | GGACTCAATAAATAG[C/T]TTACCAAGGAAATAA | 93664 |
rs189591056 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122689483 | TACAGTAATGACACC[C/T]GCTCCAGGAACAGTT | 93664 |
rs189596936 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122674508 | ACCAAAGAAGTCACT[A/G]AATATCTTAACAAAG | 93664 |
rs189609520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122659602 | AATAACAGCAGTGAA[C/T]TTTCCAAAATTAATA | 93664 |
rs189610773 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | CADPS2 | GRCh38.p7 | 7:122423767 | ACAAATTGCTTGGCA[C/T]CATTCCGAATTTCTG | 93664 |
rs189613805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122342742 | ATTCAGTATAATGTG[C/T]GTGTAACCATGTTTT | 93664 |
rs189613991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122775667 | ACCATCCAGAATTAA[C/T]ACTATAAATGATATC | 93664 |
rs189624133 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122815157 | TACAATAAAGAAAGT[A/G]GTTTGAGCGTGTTAC | 93664 |
rs189625175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122498737 | GTTCACTTTGCATAC[C/T]GTTATTTTCTTTTTT | 93664 |
rs189628794 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122483353 | GAAAGTGGAGCAACA[A/C]CTTAAAGTACTAAAA | 93664 |
rs189631964 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122456113 | TCTCTAAAGTTAGTA[C/T]GTATTCACACTTAGC | 93664 |
rs189633997 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539149 | AGTTCATGTGTCAGA[C/T]ACTTAAAACCTAATG | 93664 |
rs189635581 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122490957 | TGGGGAGAAAATTAG[C/T]AGTTATAATATAATA | 93664 |
rs189637655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122518866 | TGTGAATTTTTTTCA[C/T]GTGATTTTAAAGAGG | 93664 |
rs189641486 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122449094 | AGGCAAGTGAGCATG[A/C]AAATTTATTTATTGT | 93664 |
rs189641786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122474893 | AGCAATGATGCCTAG[A/G]AGTCTGCTTTCCAAA | 93664 |
rs189646759 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122847308 | GCCAGGCTGGTCTAG[A/G]ACTCCTGAGCTCAAG | 93664 |
rs189648215 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122436901 | TGTATCCGTGGACAA[C/G]TTAATAGTCAAAAAT | 93664 |
rs189650136 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122382700 | GGCTCATGTCTGTAA[A/T]CCCAGCACTTTAGGA | 93664 |
rs189651300 | snp | A/C | 0.185472 | 0.241529 | intron-variant | CADPS2 | GRCh38.p7 | 7:122721604 | CAGCCGAATTCTACC[A/C]GAGGTACAAGGAGGA | 93664 |
rs189654943 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122848639 | TCAAATGCCTGTTTT[A/T]TCCCCATTATACTGT | 93664 |
rs189657906 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122400024 | GTTACAGGTGTTCCT[A/G]TGATCTGTTACAAGA | 93664 |
rs189658345 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122587557 | TCTTTGCTGTTGTGA[A/G]CAGTGCTGCAATGAA | 93664 |
rs189660679 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122343703 | TTTCAACATAGAAGA[C/T]GTGCTTTAGCTATTC | 93664 |
rs189662354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122420588 | GCCCCATTAAAAAGC[C/T]GAACATTGGGAATAT | 93664 |
rs189665978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122726272 | CCAATAAGTACTTTG[A/G]TAATCAATACAAAAT | 93664 |
rs189670060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122759670 | ATGATTTTAATGGAT[C/T]ACTGAGTAGTATTCA | 93664 |
rs189674160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122740931 | AAATTAAAACTGTAT[A/G]AGAAGCCATTTTAAA | 93664 |
rs189676131 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122706290 | TATATTCAAGGAATA[C/T]ATATATGCTTATATA | 93664 |
rs189677561 | snp | A/G/T | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122619533 | TCAGGAGGCTGAAGC[A/G/T]GGAGAATCACTTGAA | 93664 |
rs189678134 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122803451 | TCTCATTTTGGAGTC[G/T]GAAAGAACGCTACAT | 93664 |
rs189685808 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122781509 | ATACATAAGAGATTT[C/T]ACATTTATTTCCTTC | 93664 |
rs189690659 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122819019 | CCTCAAACCCCACAA[C/T]AGGATTTAATTAACC | 93664 |
rs189697776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122656231 | CCCACAAAGTTCTAA[C/T]AGTGAGGATCCAAAA | 93664 |
rs189705039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122518394 | ACATATAATGGAAAT[A/G]GCATTAATTTAACAG | 93664 |
rs189710609 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122887470 | TCTGGCCTCAAGTCG[G/T]CGTCTTGTAGCTGCG | 93664 |
rs189718030 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122623817 | AGAGTTTAACAAAGA[A/C]AAAGGCGAGCATGTC | 93664 |
rs189724366 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122597954 | CACAAACATGGGACA[C/T]TATTCTAATAAAATA | 93664 |
rs189731167 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122694451 | AGAGTCACCCTGGTC[A/T]TCAACAGTGATGAAA | 93664 |
rs189732554 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122684173 | GAAATAGGCTGTAGG[A/C]ACTTGACTCTTACTT | 93664 |
rs189732873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122679503 | GATTCTAGTTTCACC[C/T]TGACCTTGTGATCTC | 93664 |
rs189746495 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122480007 | TAACTGAGAGACAGT[C/G]AAAACCAGGGTGTGT | 93664 |
rs189753346 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122590026 | TTCCTTATTTAAGAT[A/G]TTTGCACTATGCAAA | 93664 |
rs189769847 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122610404 | TAAGTATCAATTAAA[G/T]ATAAGATTCTGTAGA | 93664 |
rs189798142 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122805392 | CTCAATCTCCTGACC[G/T]AGTGATCCGCCTGCC | 93664 |
rs189798663 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122556318 | AAAAGACTAAGATAG[A/T]TCTCTATATCCTCTG | 93664 |
rs189800897 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122575840 | CTATAGACGTTTTAC[A/G]TTTTAGAATAATTTA | 93664 |
rs189802611 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122374315 | GTGGTGAAAAAATAA[A/C]TTTTTTCTCTAAGAT | 93664 |
rs189807417 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122836619 | CAAAAAAAGGAAGGG[A/G]TTGCAATCCTAGTCT | 93664 |
rs189808006 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122652347 | TTTAAAAATAACTTT[A/T]CATAAACACATTTGT | 93664 |
rs189809022 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122595416 | GGGCCAGTCATTTGG[A/G]GTTATAAAAATGTTT | 93664 |
rs189813206 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122766385 | CATAAATGCAATATA[C/G]AGTGACTATTAGCCA | 93664 |
rs189814490 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122332314 | AATATTTGTTCTACT[A/G]TAGTAAAACAATGTA | 93664 |
rs189814605 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122776538 | TGAGGAACAGGCAGA[C/T]TGGAACAGTTTGGAG | 93664 |
rs189821336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122384919 | CAACAAATCTGTTCA[C/T]CCACTCAGCAAACAT | 93664 |
rs189823043 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122837764 | TAGACCAATAACAGG[A/C]TCTGAAATTGAGGCA | 93664 |
rs189828142 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | CADPS2 | GRCh38.p7 | 7:122785946 | AGATGCAGGTAATGT[A/G]GTTCTAAAAGAAGAA | 93664 |
rs189829344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122727458 | CACCTATATAGATGT[A/G]CTATCCTTTTTTAAG | 93664 |
rs189831071 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122878246 | GCCTGGCGACAGAGC[A/G]AAACTCCGTCTCAAG | 93664 |
rs189835527 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122681574 | AAGTAGTCAGGAATC[A/G]ATCTCGTGAAGCCCG | 93664 |
rs189837730 | snp | C/T | 0.000480287 | 0.0154891 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122702399 | CCTTCTCTGCTGCCA[C/T]GTTGATTTTATGTGT | 93664 |
rs189842801 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | CADPS2 | GRCh38.p7 | 7:122824997 | GCCAAGGAAACGAAA[A/G]AAGTAACAGAGACAT | 93664 |
rs189843028 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122808520 | TAAACCACTTGCTTG[G/T]TCTAAGACAGCCCAC | 93664 |
rs189846491 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122326617 | TATACACAAACATAA[C/T]GACAGTCCAGATCAC | 93664 |
rs189851033 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122839102 | ACCAATGGAACAGAA[A/C]AGAGCCCTCAGAAAT | 93664 |
rs189856503 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122638317 | TTCTGAGAGGGAGGG[C/T]GTCCTCCCCACCCCC | 93664 |
rs189870066 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122438654 | CAATGCACTTCCCAA[A/C]TGAGAATGTAATCCT | 93664 |
rs189876261 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122469058 | TGCATGAACATATAA[A/G]CATACCTTGAATTAC | 93664 |
rs189877458 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122736854 | AATTCACAGCCTTCC[G/T]GTCAGACCAGCAAGC | 93664 |
rs189883365 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122682472 | TAAAGAAAATGTTTT[A/T]CTTGTTTTGCCCTCA | 93664 |
rs189884973 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122668774 | ACCAGGTCACTTTTG[A/G]CAGACAAGATTTACT | 93664 |
rs189895177 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122654129 | AAAGGTAAGGAAGGT[A/G]TAGAAGAAAAGTTTG | 93664 |
rs189897250 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122514575 | GGGAGTGTAACATCT[C/T]GGGAGATGATCTTCT | 93664 |
rs189900796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122834233 | AATAACTAAAATTCA[A/G]AGCCTAACCTTTGGG | 93664 |
rs189903231 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122402418 | CCCCCCGCCCGAGTT[C/G]CTGCCTCTAGGCATT | 93664 |
rs189905458 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122579376 | GGAAACCCTGTAATA[G/T]ATAGAAAAGTTGTCT | 93664 |
rs189920551 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122869903 | ACAGCCTGTTATTAG[C/T]ATAAAATGTTTTATG | 93664 |
rs189927840 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122541399 | TTAGCAGAGATGGGG[A/T]TTTACCATGTTGGTC | 93664 |
rs189961316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122640156 | TCGACTTCTCTCTCC[C/T]TCACAGTCCACATCC | 93664 |
rs189981747 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122699348 | ATTAAATCTAAAATT[C/T]ATACAATGTGTGCTC | 93664 |
rs189988116 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122670442 | CAGGGGTGGTGACAC[A/T]TGCCTGTAGTCCCAG | 93664 |
rs189992514 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122332722 | TTCAGTTACATAACA[C/T]AATAAGTTCGAAAAC | 93664 |
rs189995142 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122699668 | CCTGCTCAGTTTACT[G/T]CTGCCTCACTTTCTC | 93664 |
rs190006592 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122724171 | ACCCTATAACTTAAA[A/G]TATAATAATAATTGA | 93664 |
rs190012260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122606263 | TTTCCTTTGTAAAGC[A/G]GGAGAAGGATGACTG | 93664 |
rs190013191 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CADPS2, RNF133 | GRCh38.p7 | 7:122697319 | CAGCACAATAACCTC[A/C]CAACTAAGACATACT | 93664 |
rs190015162 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122709500 | GGAAGCCAGTGCAGC[A/G]ATTCCTCAGGGATCT | 93664 |
rs190017508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122725853 | ATACTGAAACAGGAA[A/G]TACTTAAGAGCAAGG | 93664 |
rs190024003 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122690193 | ACTAACCAGGGTAAA[G/T]CACGTCCCTCAGGCA | 93664 |
rs190035785 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122737156 | TTTGCTGTATATTAG[A/G]TTTCACATCTAGAAT | 93664 |
rs190057303 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122353467 | GTTTCTTCTTCCTTC[C/T]TCATTGTTTTGGTCT | 93664 |
rs190058612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122629054 | ATTAAGGATGAGTAC[A/G]TAAAATGAATAATAT | 93664 |
rs190061660 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122755136 | GCAGTATGATGACAA[C/T]TACACCAAATCTAGA | 93664 |
rs190065531 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122821546 | GATACTTTCACTGGA[C/T]AGGTAGAGGCCTTTC | 93664 |
rs190068174 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122613385 | GATACTGGCATTGCA[C/T]GTCAGGCAAGAAAAT | 93664 |
rs190075808 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122857631 | AGATTTCCTATTCAA[A/T]CAAGTTTCCCAAACA | 93664 |
rs190085550 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122596221 | TACACACAGGCTTTT[A/C]AGCTCAAGAACATTT | 93664 |
rs190087479 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122675569 | AAATAATGCTGCAAT[A/C]AACATATGTGTGCAT | 93664 |
rs190089988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122829070 | TCATCTCTAAATGAA[C/T]ATTCTAAAATACAAA | 93664 |
rs190093500 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122659972 | CTGAGAGACTGCATC[A/T]CCACTAGTCTTGGCC | 93664 |
rs190093816 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122611513 | TACTTTTGCACCAAC[A/T]TAACAGGAAAACACA | 93664 |
rs190097921 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122489020 | TTTATTTTACCTTTT[A/C]AGATGACAATGCTAC | 93664 |
rs190099748 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122875789 | GGCCAAACTGCACTT[A/C]GAGATAAATTCATAG | 93664 |
rs190100685 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122645605 | GATTATATATATATA[C/T]ACACACACACTAAGA | 93664 |
rs190105735 | snp | A/C | 1.72591e-05 | 0.00293756 | missense | CADPS2 | GRCh38.p7 | 7:122474489 | AGAAATAAACTCATC[A/C]ATACCATGTTTCTGA | 93664 |
rs190110025 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122508555 | CTGCAGCCTTGAACT[A/C]CTGGCCTCAAGTGAT | 93664 |
rs190110158 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122428608 | GAGTAGCTGGGACTA[C/T]AGCCATGCACCACTA | 93664 |
rs190110497 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122427678 | CCTATGCTTGTAGTC[A/G]TCTGCCGGATCATGG | 93664 |
rs190116454 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122864024 | GACAGGGCGAGATTC[C/T]GTCTCAAAAAAAATA | 93664 |
rs190118367 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122446665 | CAATACTTAACAGGA[A/G]ACTCCAGGGAATCAT | 93664 |
rs190124201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122408986 | AGATTTGAGAGTTGG[A/G]GACATTTTAATGCCT | 93664 |
rs190126871 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122396134 | TTTTTAAACTTATCA[A/G]TAAGGTAACTGAGGC | 93664 |
rs190128466 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122455017 | GACAGTATTCCTTGA[A/C]TCAATTCCTGTAATG | 93664 |
rs190132203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122784154 | CATGACCCACTATTT[A/G]TCATCTCACATCCCC | 93664 |
rs190143670 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122559870 | AAAAGGGACAAGACT[A/C]TATAACTGAGACCAG | 93664 |
rs190145096 | snp | C/T | 0.000703628 | 0.0187435 | intron-variant | CADPS2 | GRCh38.p7 | 7:122388776 | ACATCATGAACTCCC[C/T]GTTAATTAGGTATAC | 93664 |
rs190145428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122436043 | AGTTCTAGGGACCTA[C/T]TATACAGCAGAATGC | 93664 |
rs190147973 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122532785 | TACAGTTATATTTCC[C/G/T]GAGAGTACGATAAAC | 93664 |
rs190154398 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122357582 | TGTATCTACCATTAC[A/C]ATATCATACAGAATA | 93664 |
rs190158762 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122759129 | CATTTTCCCTCTAAG[A/T]GGAGAATCACAGTCC | 93664 |
rs190165913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122597400 | CTGCTATGGTCTGAA[C/T]GTATGTGTCCCCCTA | 93664 |
rs190176603 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122710625 | ATTCAATAAATGGGC[C/G]TTCCTTCCTCTTCTC | 93664 |
rs190182454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122724421 | CCTGCTCTGAAGCAG[C/T]TTATAATTATCACAA | 93664 |
rs190184009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122494869 | AAATGAAAGTCAGTT[A/G]CTCCCATAAGGGTTT | 93664 |
rs190208487 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122607387 | CTGTGGTAAGAATTA[A/C]GCTTCCTACTTAAGC | 93664 |
rs190229203 | snp | C/G | 0 | 0 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122553678 | TCAGTTCGCTCCACC[C/G]TGATGTTAGTGATTG | 93664 |
rs190232822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122391276 | AGAATGGTGAAAGCA[C/T]AATCACTTTACTTAC | 93664 |
rs190243960 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122571956 | AATAATTACAAAAAA[A/T]TTAATAATCACTTTA | 93664 |
rs190246335 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122531694 | CCCAATATATGTATT[A/G]TCCCTTGTAATAAGT | 93664 |
rs190248902 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122684595 | TTATATTTTATAAAA[C/T]ATTCCACAATGGATG | 93664 |
rs190251567 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122835406 | AGGAACGCAGCTCCT[A/C]GCCAGCAATGGAACA | 93664 |
rs190252245 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | CADPS2 | GRCh38.p7 | 7:122592779 | ACTCATAGGTGGGAA[C/T]TGAACAATAAGAATA | 93664 |
rs190258833 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122570336 | AACCACAATGAGATA[C/T]CATCTCACACCAGTT | 93664 |
rs190260100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122495832 | TTTTAAATCTTTTTA[C/T]TTTTTGCCAACTTTG | 93664 |
rs190262013 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122432981 | AACTAATATATATAA[C/T]ATATTTTTTGGAGAC | 93664 |
rs190262644 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122493590 | GTGTGGGTGACAGAA[C/T]GAAAACTGGTGTGGA | 93664 |
rs190267930 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122450168 | GTTAAATAAAATATT[C/T]TTGTGAACATATTCA | 93664 |
rs190268719 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122533454 | GTACACCCATGGTCT[A/T]AAATTTTTGTAACCA | 93664 |
rs190274990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122516891 | CATGTCTTCCTTTTA[C/T]TGTTTGAGTAGTTTA | 93664 |
rs190278313 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122414003 | CAATCAGAGTAGATT[A/G]TATTTTAAATTCACA | 93664 |
rs190283055 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122469930 | GTCTGAATGAGTTAA[C/T]TGAAGTCTTCTAAGA | 93664 |
rs190286638 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122712570 | TGAGGTCATGGTTAT[A/T]TTTTTTCCAAGGAAC | 93664 |
rs190288452 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122393131 | TCTAAACACATCTGC[A/G]CAGAACACAGCCCAG | 93664 |
rs190290180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122375083 | ATCCCATGTTCATGA[A/G]TTACAATAATTATTA | 93664 |
rs190297858 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122478287 | AAATTTTAGTTCAAT[C/G]TGTCTTCTGAAACAA | 93664 |
rs190298351 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122755906 | AGACGTTTTCCTGGA[C/T]TCCACATTAAATTAT | 93664 |
rs190298962 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122631587 | CCTGGTCTGTTTTTT[A/T]AAAAAATAATTAATG | 93664 |
rs190304558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122354525 | ACAACTTTTTACATA[C/T]ATTTGCTATCAGCTA | 93664 |
rs190306388 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122729873 | GGTAACTGGAATGAA[A/G]AGGAGCAGCAGCAGA | 93664 |
rs190307169 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122333272 | TTGGACTCTTGGAAC[C/T]GCTATTAAATGGTAC | 93664 |
rs190307430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122777716 | CTCTGCACTTCTCCT[C/T]GCAGCCACCTTGAGA | 93664 |
rs190308196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122344097 | CAAACTGACAGTGAA[C/T]ACTGACACGAGAGAC | 93664 |
rs190314394 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122747391 | AAATTTCTACCCAAC[A/G]CTTTTCTACAAATAA | 93664 |
rs190314655 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CADPS2 | GRCh38.p7 | 7:122318549 | TTTGGGATAGCATGA[C/T]TGGACATTTGAGGGT | 93664 |
rs190315557 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122738077 | AAATGCTCTGAACTG[C/G]GGAAGTTTACAACCA | 93664 |
rs190316212 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122718946 | GCTGGATTTATGATA[A/C]TAATTACTTGCCACC | 93664 |
rs190326051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122799180 | CTCACATTTGGCCAA[C/T]TGCCTTGGCAATAAT | 93664 |
rs190326474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122781107 | CTCATGACTAAAATA[C/T]TATTAATCTGATGGA | 93664 |
rs190327202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122662666 | GCGTGAGCCACCATG[C/T]CTGGCCTTTATCCCA | 93664 |
rs190333861 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122765201 | GAAGGCTCACAGTTA[C/T]ATTTTACTCCAGCAA | 93664 |
rs190342363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817492 | CCAAAACTCTGGCGC[C/T]GGTCACAGACTGGGA | 93664 |
rs190345319 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122811311 | TGGCTGCCTTCCAAG[A/T]TAATCTGGAGGGGTG | 93664 |
rs190345328 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122445003 | CCGGTAGCATCTGTC[A/G]GAAAAAAGTATACTT | 93664 |
rs190349363 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | CADPS2 | GRCh38.p7 | 7:122841822 | TAAAAGTTTAGTACT[C/G]TATTTTTTTTACCCT | 93664 |
rs190351333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122663129 | TTTTGCTCAACTTTC[C/T]AAGTAAAGTGATTAT | 93664 |
rs190351706 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122785507 | ACCCCAGGTGAATTT[G/T]GAACTAGAGCCCTAA | 93664 |
rs190367092 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122720484 | TATATGTATGTATGT[A/C]TATATGTATATGTAT | 93664 |
rs190369974 | snp | A/G | | | upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122886835 | CCGCCTGGAGCCCTA[A/G]CACACAGTTTGCAAA | 93664 |
rs190383971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122692428 | AGCACAGTTACAAAC[A/G]CCCATGTGACTCTGC | 93664 |
rs190386268 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122703934 | TTACAGAATCTTTAC[A/G]GCTTTAAAGATGCCT | 93664 |
rs190389376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122377732 | GTTCACCCCTTCCCC[C/T]CATGGTTTTCCTATT | 93664 |
rs190394615 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122690581 | TTTAGGGGTATTGGG[G/T]CAGGTAATAACAGAT | 93664 |
rs190395426 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122487981 | CATTTATGAGATTGA[C/T]GCTAAATGCACACAT | 93664 |
rs190397426 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122675922 | GCAGCAAACCACCAC[A/G]GCACATGCACGCCCA | 93664 |
rs190401753 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122740069 | GAACAAAATCCAGAA[C/G]ACAGAAAACACTTGA | 93664 |
rs190407272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122780877 | TGGTTTTGGTTTTAT[A/G]TGACTACAAACAATG | 93664 |
rs190411548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122337280 | CTGTTTAAGCCTCTG[C/T]TGTTAATTAGCTGAT | 93664 |
rs190435909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122453864 | GCTTGTGTCAACCTT[C/T]GCTAAGAAAAGAATG | 93664 |
rs190436488 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122843767 | AATGAAGAGATGGTA[A/G]AGAGGGCCATGGGTC | 93664 |
rs190440597 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122418099 | CGCTTGAACCTGGGA[A/G]GCAGAGGTTGCAGTG | 93664 |
rs190456724 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122818169 | GGCTTGCTTCCTTCA[C/T]TATGGGCAACCTTCC | 93664 |
rs190459825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122589946 | TAATCATCTCAAGTA[C/T]AGAGCACTGAATTTT | 93664 |
rs190466654 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122883489 | AATAAAATAAACAAC[A/G]GATTAGTGATTTTGC | 93664 |
rs190468560 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122378173 | CCATAATTTGCTTTA[C/T]CTTTTCCCTCATTAG | 93664 |
rs190473204 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122853278 | CCTCTACTCCATGTG[C/G]CATTTGCAGAGTGGC | 93664 |
rs190477039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122384497 | TATATGTAATGTATA[C/T]ACTAATTTTCAACAA | 93664 |
rs190491643 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122364055 | AGCCCATGCTCTTTA[C/T]CCATCATGCTACAGA | 93664 |
rs190493505 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122551112 | GCTTTAGATTGGATG[A/C]ATTTTACCTTCTGGT | 93664 |
rs190498355 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122628379 | ACACAGGATGTATGC[A/G]TAAACATTCATTAAA | 93664 |
rs190523108 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122483995 | CATGGTATTCACAGA[C/T]TGGAAGACTCAATAT | 93664 |
rs190524697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122673096 | GGTTCGTGGTCTTGC[C/T]GGCTTCCGGCTTCAG | 93664 |
rs190526431 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | CADPS2 | GRCh38.p7 | 7:122592871 | GAGGAATAGCATTAG[A/G]AGATATACCTAATGT | 93664 |
rs190530059 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122449780 | CAACAGTGTTTCCTA[A/G]TGTAAATTTACTGGC | 93664 |
rs190532264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122513180 | AAATTTTGATAGATA[C/T]AACCCACATAAACAA | 93664 |
rs190532768 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122693013 | CCCATGTTATGGCCA[A/C]ATGGCTGTGATAACA | 93664 |
rs190535109 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122705713 | ATAATATATCATATA[A/T]TATATAATATATCAT | 93664 |
rs190535191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122607674 | TTCAGATGCCTCTCA[C/T]TTTAAAGATCCCCAG | 93664 |
rs190538817 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122484599 | GGCAAAGATCCTTTA[C/G]TTATAACATCAAAAG | 93664 |
rs190539657 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122555456 | ACATCTAAGCCTTAA[C/T]ATTTTTAAATGGGAG | 93664 |
rs190540618 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122657468 | TTCCATTTGTTTGTG[C/T]CCTCTTTTTATTTCG | 93664 |
rs190543881 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122625882 | ATCTACCTAGATATT[G/T]GTCTAGATATATGAA | 93664 |
rs190545202 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122642397 | TGTTGCATGGGAGCA[G/T]CTCTGGGAAATAGGA | 93664 |
rs190550577 | snp | C/T | 0.000258331 | 0.0113622 | intron-variant | CADPS2 | GRCh38.p7 | 7:122471612 | TTTCTTTCTATACTA[C/T]GATTTGCTTTCCTGA | 93664 |
rs190553514 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122732294 | GTATTAAAGTAAACC[A/G]AATATCTGAAGGTAC | 93664 |
rs190556094 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122594394 | ATAAGAAAAATCCTG[C/G]AAGCTTTATCTGCCT | 93664 |
rs190560556 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122504289 | TTACACAGTGGTCTC[C/T]CCGTGAATCTAATTC | 93664 |
rs190564073 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122572017 | TATATTGGGGATTTA[A/G]GAATGCCAGCATTAT | 93664 |
rs190565854 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122450748 | CCATTTTGCCCTGTC[C/T]GGTCTTGAACTCCTG | 93664 |
rs190581277 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122433601 | AGAGACAGGGTTTCA[A/C]CATGTTGGTCAGGCT | 93664 |
rs190586386 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122677009 | TAAAAGGACACACTT[C/G]TGTAGCCCTCCACAC | 93664 |
rs190607604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122648102 | TACCAGACTTGGTAA[A/G]CAGGTGGCATAGAGA | 93664 |
rs190618849 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122705264 | TGTGACTGGGAGACA[A/G]AGAGAGAGACTGGAT | 93664 |
rs190622654 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122835606 | GACCTGATGGAACTG[A/C]AAACCATGGCATGAG | 93664 |
rs190623793 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122734514 | AGGTAATAATACTTG[C/G]ACTGTTTATTGCAAG | 93664 |
rs190627411 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | CADPS2 | GRCh38.p7 | 7:122773084 | AACACGAACAATTCA[C/T]GAATTGCTAAATTAT | 93664 |
rs190629618 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122851281 | AGGGATGTTCAACTG[A/G]GCCACTGAGGAGTCC | 93664 |
rs190633759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122872751 | GTAAGAATACAAGTT[C/T]CATGGCAGCAGAATT | 93664 |
rs190639469 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122686156 | AAACTGTTCATACTT[C/T]TCAGTTTTTTTCTAT | 93664 |
rs190641138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122507441 | GGTGCCTTTGGTGGG[A/G]GTATCTGGTGACTTG | 93664 |
rs190646808 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122733865 | CCCATTGCTTGAGTC[A/T]AGGATTTCTAGGCCA | 93664 |
rs190649694 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122657166 | CTGTTCCATAGGTCT[A/G]TATCTCTGTTTTGGT | 93664 |
rs190659334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122752405 | CTCTGAAATGTACCT[A/G]GATAACACTGTGAAA | 93664 |
rs190661720 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122713865 | TTTAAAAAACAAAAA[G/T]GTCTTTTTTGTTCCC | 93664 |
rs190669393 | snp | A/C/G | 0.0283406 | 0.115616 | intron-variant | CADPS2 | GRCh38.p7 | 7:122721366 | GGGGATATCCCCACC[A/C/G]ATCCCACAGAAATAC | 93664 |
rs190671432 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122687310 | CCTCCAGCTAGCACT[C/T]CCAATGCCTTTAGCT | 93664 |
rs190674745 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122435591 | TGTAATTAGGTGCAG[C/T]CACTATGAAAAATAG | 93664 |
rs190676255 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122770156 | CTCAGCACACCTTAC[A/C]TCACTTAAATAAGAA | 93664 |
rs190680581 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122473305 | CGTCACTTTCCTTTT[C/T]CTGTCTATAAAGCTT | 93664 |
rs190688961 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122802856 | ATTAGGGACAGGAAT[G/T]AAAGCAAATGGAACG | 93664 |
rs190704225 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122836465 | GGGCTAAATCCTCCA[A/C/G]TTAAATGACACAGAC | 93664 |
rs190708392 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122396663 | ACGATTCAATATACA[C/T]CTGCTCCTCAAATCC | 93664 |
rs190715031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122543892 | CTATAAACAAAAACA[C/T]GTGAAAAGTATCAAA | 93664 |
rs190717138 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122523719 | TAAAGCATGGTTTCA[C/T]GTTTTTCCTCAATTT | 93664 |
rs190723017 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122481641 | GCTACTTGGGAGGCT[G/T]AGGCATGGGAATCCC | 93664 |
rs190723316 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122446278 | CTTAAAATTTTTTCA[C/T]CAGATGCTGGAGATA | 93664 |
rs190724833 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122875140 | TTGCAGATGTGTACA[A/C]GTTTGCAGATGTGTA | 93664 |
rs190737645 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122812926 | ACACTGAAAACACAT[A/C]GGATGTTTTTAGTTC | 93664 |
rs190739307 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122371285 | GAAACACCCAAGACT[C/T]GGTAATTTATAAAGG | 93664 |
rs190746954 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CADPS2 | GRCh38.p7 | 7:122860496 | TGTCATCCTCCCAAA[A/G]TGCTGTGATTACCAG | 93664 |
rs190748110 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122351177 | AGAGACCATCCTGGC[C/T]AACACGGTGTGTTAC | 93664 |
rs190752345 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | CADPS2 | GRCh38.p7 | 7:122327354 | TTCTACCACACCACA[C/T]TCTAGATAATTTGAA | 93664 |
rs190752382 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122819407 | ACTGACACTGCCCGA[C/T]CGCCTTGGAAGCCCC | 93664 |
rs190753699 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122408547 | CTCATCCCTCAGCCA[C/T]CCAAGTAGCTGGGAC | 93664 |
rs190757825 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122875668 | TTTTTCAACTGCAAT[C/T]TCTAAATTACTCTTC | 93664 |
rs190758005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122370885 | TACTGTGAAGGGACT[C/T]GTAGGTGATGCTAAA | 93664 |
rs190760888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122495196 | ATATATTCATCATTC[A/G]GCTTTGTTGAATGGT | 93664 |
rs190760976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122880897 | TTGTCCCACTGATAT[A/G]TCCACTATTTAATTA | 93664 |
rs190761847 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122843685 | CTGACAAGAGAGACT[A/G]GGGAATGCTTGACTT | 93664 |
rs190763807 | snp | A/G | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122609914 | ATGAATCTCTTTCCT[A/G]TCATGCAAGATGAGT | 93664 |
rs190764978 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122461208 | TACGTAGATAGAATA[C/T]ATTTTAGAGACATTA | 93664 |
rs190767416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122477841 | AACAGTACGATTGTA[C/T]GGATTCTAGTTGTCA | 93664 |
rs190774886 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122855192 | GGGATCATTTCTTTA[A/G]TATAGTAGTAGTATT | 93664 |
rs190781590 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122440603 | ATCTCCCAAGTTCTT[A/T]AATCAATGAAATGGA | 93664 |
rs190794120 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122575513 | ACGATCTCGGCTCAC[C/T]GCAACCTCCCCCTCC | 93664 |
rs190812251 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122620226 | AAGAATGAGCTATAA[A/G]CCTCAATATAATTTT | 93664 |
rs190823949 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122538319 | TGAAATTTGGCAGTG[C/G]AGGTGAATATAAACA | 93664 |
rs190837156 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122524635 | AATAGTGTATGTGGT[A/G]TCTCCAAAAGTGCAG | 93664 |
rs190845913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122738276 | TAACAATTTCAAGAC[A/G]GCAGGAACAGAGAGC | 93664 |
rs190855353 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122561874 | TATTGTAAACACTCA[C/T]CAAGTATTTGTTGGT | 93664 |
rs190855740 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122544190 | TCAAATGTCCATTTT[C/G]ATGAAATGGATAAAG | 93664 |
rs190864710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122511383 | GATAAGGGGCAAAAG[A/G]TTACTTGGAACCTTA | 93664 |
rs190874971 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122549118 | AGAATATCATAAGGC[C/T]GAGCACAGTGGCTCA | 93664 |
rs190882687 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122753332 | CTACATTCACCCTAC[A/C]GTTTTCTAAATACAT | 93664 |
rs190885207 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122797633 | ATCATTTATAAGTGG[A/G]AGCTAAATGATGAGA | 93664 |
rs190887111 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122364635 | AGGAGACTGAGGCAG[G/T]AGAATGGTGTGAACC | 93664 |
rs190893402 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122835001 | CTCAAGTGGGTCCCT[G/T]ACGCCCGAGTAGCCT | 93664 |
rs190896475 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122672316 | TCCAGGCGTCGGTGG[C/T]CACCCTCCAACTTTC | 93664 |
rs190903446 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122864461 | CTCGAGCCTGGGCAA[C/T]AAAGTGAAACTCTGT | 93664 |
rs190907574 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | CADPS2 | GRCh38.p7 | 7:122319404 | AGAAGTAGTTATGAG[A/C]AAATAGATTTTTATT | 93664 |
rs190908949 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122887111 | TGCGACAAGACTTTG[A/G]AAAGTCTCACTCTGC | 93664 |
rs190919817 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122871405 | TGACAATTTTTAATT[A/G]TTATAAAACAAAAGC | 93664 |
rs190923242 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122381290 | CAAGAGGAAATTAAA[C/T]GCCACGTGATACACC | 93664 |
rs190930385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122700357 | AAAGGGCCCTATGGG[C/T]CAACAAAAACTAGTA | 93664 |
rs190935444 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122406474 | GGGCTGCAGGAAGAC[A/C]GGGAAGAAGGAAGGA | 93664 |
rs190936104 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122361153 | AGGTCAGACTAACTT[A/G]TGATGTTTACTCTTT | 93664 |
rs190937707 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122339600 | TAGCTCAAAAGTTCC[A/G]GGCAGGCCGGGCATG | 93664 |
rs190947653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122387462 | TACCACATTTAATGG[A/G]AAAAAAACTCATAAT | 93664 |
rs190955583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122730768 | GTACTATTTTTAGAG[C/T]AGTTTTAGGATGACA | 93664 |
rs190960418 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122793913 | CCTGAAAACAAACTC[C/T]AGGTTGGAATTTCTT | 93664 |
rs190961179 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122466388 | TAGGCTCCTGCTTTT[C/T]GCTGTCTTTGCCACT | 93664 |
rs190965742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122771936 | CAGATTTGTGTTAGG[A/G]AGAGAAAAATCAGGT | 93664 |
rs190973230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122761873 | TGTGGTGGCATGCAC[C/T]GGTAATCCTAGCTAC | 93664 |
rs190974554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122812250 | AAAACTGAAGTAAAA[A/G]AAAATAAGTAGCACT | 93664 |
rs190978599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122755577 | TTATTAAAACAAAAG[A/G]ACTTCCAGTACATAA | 93664 |
rs190983862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122617784 | CACAGTGGCTCACGC[C/T]TGTAATCTCAGCACT | 93664 |
rs190986275 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122843126 | CCGAAGCTGGAAAAA[C/G]AAAAGCCTTCATTAA | 93664 |
rs190986477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122829961 | ATGAGATACCTATTT[A/G]TGTATAAAATGAGGT | 93664 |
rs190988603 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122427973 | TTTCTTCATAGAGGT[C/G]TATAAAGTTTCGCAT | 93664 |
rs190988641 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122854235 | AGTGGTGGGTGACTC[A/G]TGCCTGTAGTCCCAG | 93664 |
rs190988911 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539586 | ATTCAATGCTCTGTG[C/T]TCCAAATCCTAAGGA | 93664 |
rs190990895 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122794824 | AAGAAATTCACTCAA[A/G]ACCATACAATTAGAT | 93664 |
rs190994460 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122831082 | AGAGAAGTTTAGAAG[C/T]TGTGCTAGAAGAAGC | 93664 |
rs190996399 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122388430 | TTACATGGGTCCCCA[G/T]AATTTAATCAAGATA | 93664 |
rs191005407 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122577005 | ACCTCAGGTGATCCC[A/C]CTGCCTCGGCCTCCC | 93664 |
rs191007485 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122500426 | TTAAAAAAAAACTAA[C/G]AGTTTAACAGCACAC | 93664 |
rs191012601 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122865276 | TGCCAGCACCATGCT[G/T]CTTGTATGGTCTGCA | 93664 |
rs191019341 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122649673 | TGCCACCCATGTGCT[C/T]CTGCTGTACAGTATA | 93664 |
rs191020725 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122350236 | AAATAACATGTCTTC[A/G]AAATTTGAAATTGTA | 93664 |
rs191023230 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122582724 | TCTCATGACATACCC[G/T]TTTAAATTCAGTGTC | 93664 |
rs191026875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122671908 | TTTAAATAATTAATG[A/G]ACCAGTAAGGTTTAC | 93664 |
rs191026910 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122634388 | TTCACTTCCTGCCTG[G/T]TTCAATCTTGGGAGG | 93664 |
rs191029034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122599664 | GCAGATTTTGTCAAC[C/T]GTAGAATTTATTTTA | 93664 |
rs191036525 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122466749 | TATTGAGTAGGTAGC[A/G]TTAATGTTATTACTC | 93664 |
rs191036763 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122657110 | GTTTGTCAAAGATCA[C/G]ATGGTTGTTTATGTG | 93664 |
rs191087765 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122669483 | TGTGGGAAAAGAACC[A/T]GGGGATGGATAAATA | 93664 |
rs191089464 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122718270 | CTGCCTGTCAGCATT[A/C]TCCATCATATTCCTA | 93664 |
rs191090966 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122568267 | ACAACAATAACAACA[A/G]AAAGAAAGCTGAGGC | 93664 |
rs191101294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122604041 | ATATCAAATAATCAT[A/G]TTGGATACCTTGAAT | 93664 |
rs191108094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122746966 | CTTATTCATTGACAG[C/T]GTCTGCCTCACTCAC | 93664 |
rs191111556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122628475 | ACTATCCATCAAATA[C/T]TGGAAGTTTTTGCTA | 93664 |
rs191122540 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, nc-transcript-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122530292 | TTGAAATAAGAAAAG[A/G]TTTCCACTTAGGCTT | 93664 |
rs191123395 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122742787 | TTATTTTGGAATTCT[C/G]ATTCCTTCACCTGAT | 93664 |
rs191135169 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122619843 | CAAAAGGCTGAAAAG[C/G]CTAAGAAGAAACCCA | 93664 |
rs191142099 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122748019 | TTACTAGGATGCAGA[A/T]TTCTTCAACGCAGAT | 93664 |
rs191149932 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122344856 | TATAGAAAAGGAAGC[G/T]AATTAAGGCCTCCAG | 93664 |
rs191152082 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122849712 | TCAAGGAGCTTTCAA[C/T]TTAAAAAGCCAATAC | 93664 |
rs191161601 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122540330 | AATTTAAAAGGAATA[C/T]TAAGTTTTAAAATAC | 93664 |
rs191161949 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122639183 | TAATGTTAGAATTGA[A/C]GGGGATAAATTAGTT | 93664 |
rs191163470 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122566783 | ATCCAAACAAAAGTA[A/C]CTAATTCTGCTTTCT | 93664 |
rs191165618 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122653035 | TGCTAATCCTGAAGC[C/T]CTGGAACAAAGGATA | 93664 |
rs191165987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122588285 | TCATGAAATCTTTGC[C/T]TAAATGGTATTGCCT | 93664 |
rs191171383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122637762 | TTGCCAGCGTTTCTT[A/G]CACTGATTCTTTTTC | 93664 |
rs191179964 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122602472 | ATAAAAATGGAAATA[C/T]AATACATTGTATTGA | 93664 |
rs191185231 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122856299 | TCTCATGTGCTTCAC[A/T]TCTTGGTAGTGGTAT | 93664 |
rs191189178 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122877112 | AGAAATGCAAATATG[C/T]TTTAATAACAGGAAA | 93664 |
rs191190855 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122424984 | AATAGCTTTTTTTAA[A/G]AAAATTATTTTTTTG | 93664 |
rs191197954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122385608 | GTCAATCCTTTACGC[A/G]TAAAGGTTTTCTAAC | 93664 |
rs191200105 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122520288 | GCTGCAATGCTTATA[C/T]GACAAAACTATTTTA | 93664 |
rs191204910 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122547936 | CTAGTCTCTCTCACT[A/G]ATTCTTTCCACAAAA | 93664 |
rs191219629 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122777045 | AGTCCCAGCTACTCA[A/C]GAGGTTGAGGCAGAA | 93664 |
rs191222311 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122345460 | ACTTTTTAGTATAGA[A/C]GATACAGGATCACAA | 93664 |
rs191227195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122352419 | TTGGAATGATTCAGA[C/T]TTTGGCTTAAGTGAC | 93664 |
rs191232989 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122381493 | TTTTGAATTCAAAGT[A/G]ATCAAATGTCATCAG | 93664 |
rs191233043 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122735622 | TACACAAAAGTTACA[A/G]TGATAGTACAAAGAA | 93664 |
rs191233697 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122556749 | TTAAATAAACACTGA[C/G]TTCTTACTATGTGAG | 93664 |
rs191234958 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122784822 | TGAGTCTAGACCTTA[A/T]TAAGCCTTTTTACTT | 93664 |
rs191237085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122762289 | ACAGCAGATTCAGTG[A/G]AATTCCAGAAAGAGA | 93664 |
rs191238876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122330196 | TTGTGTTAAAATGAA[A/G]TAACGCCAAGAAAAT | 93664 |
rs191250247 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122361423 | ATTTTTAGTAGAGAC[A/G]GGGTTTTACCATATT | 93664 |
rs191251475 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122783095 | TGGGCGGGCGCCTGT[A/G]GTCCCAGCTACTCGG | 93664 |
rs191257849 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122819891 | AAACCTAATCACCCT[C/T]ACCCCACTCAACGCC | 93664 |
rs191259506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122482353 | CCAGGTGGGAGACTA[C/T]TGATACCTAGTGGGT | 93664 |
rs191265489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122519706 | CAGCTATCCTTAGGT[C/T]ACACTGTATCATCAA | 93664 |
rs191266452 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122822900 | TCTCCCTTCGCTGAC[A/T]CTCTTTTCGGACTCA | 93664 |
rs191277155 | snp | A/G/T | 0.00597598 | 0.0543831 | intron-variant | CADPS2 | GRCh38.p7 | 7:122650034 | CTGCCTCAGCCTCCC[A/G/T]AGTAGCTGGGATTAC | 93664 |
rs191280780 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122626847 | ATGTTTAGAAAATAG[C/G]TATCATGAATTTGGT | 93664 |
rs191282545 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122837446 | AGCACAACTGAAGGC[A/G]ACAGAGACACAAAAA | 93664 |
rs191286855 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122634738 | GTTCCTCTAGGTATA[C/T]TGTTAGATCGTTAAT | 93664 |
rs191299173 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122625293 | GACCTCAGGTAATCC[A/G]CCCGCCTCAGCCTCC | 93664 |
rs191304399 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122574142 | GTAAACTCATGTTTT[A/T]AAAAAAAATGTGTAT | 93664 |
rs191313172 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122593899 | TACAATAGGCAAAGT[A/G]TTACAAACTGAGATT | 93664 |
rs191316222 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122418691 | ATTTGTGAGCCATTG[G/T]TGAGTGGCTAGAATT | 93664 |
rs191319083 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122666517 | GCCGGCTAATTTTTA[C/T]ATTTTTAGTAGAGAC | 93664 |
rs191325094 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122608729 | TAAAACAGCACTATG[A/G]GATGAAGGAGAGACA | 93664 |
rs191326240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122703355 | ATGGTTCAACACTAC[C/T]GAATATGGCATTCTG | 93664 |
rs191328354 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | CADPS2 | GRCh38.p7 | 7:122683057 | TTGGTTCTTGTCTGG[A/C]GTCCAGGAAGAATCA | 93664 |
rs191344808 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122654589 | ATGGTATACTGAATA[G/T]TGAGACTTCTAAGAA | 93664 |
rs191350002 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122561038 | TAATACACTTGAGGT[G/T]GCTAAATCTAAATTA | 93664 |
rs191363565 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122484512 | TAACTGAAAATGGTT[G/T]TAAAATGTAAACGCC | 93664 |
rs191368473 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122729851 | GAGGTACTAATACAC[A/G]AGGGGTGGTAACTGG | 93664 |
rs191373933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122523527 | TGCTGATATTTATAC[A/G]ACTGTATAAATATGT | 93664 |
rs191381745 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122461664 | TAGTGGCGCCATCTC[A/G]GCTCACTGCAACCTC | 93664 |
rs191384690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122621190 | TACAGGTGTGAGCCC[C/T]AATGCTCATCTTATT | 93664 |
rs191384739 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122335032 | TCACTAGATTCCTAT[G/T]GAGTAATTGTGACAT | 93664 |
rs191386930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122738958 | GAAGCTTAACCAAGC[C/T]GAGGTGCAGGAACAT | 93664 |
rs191399359 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122725016 | TGACAACTCATTAAC[A/G]AAGTTTAAAAAGGGA | 93664 |
rs191418773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122758744 | ACCTTTCAGAATTAG[A/G]AAGTACTGGGTTCAT | 93664 |
rs191423636 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122808407 | TTATTAATCTTAACT[A/C]CTGTGACAACTTTGT | 93664 |
rs191433895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122670183 | GTCAATTGGCATATA[C/T]ATATATAAACACTGA | 93664 |
rs191434708 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122872594 | TTGTTATATTTCAGA[A/C]TTTTTTCTTATGATA | 93664 |
rs191435422 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122660835 | GAATCACCTGAACCC[G/T]GGAGGTGGAGGTTGC | 93664 |
rs191436702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122470524 | TTTTTAAGACAGAGC[C/T]TGTTCTGTTACCTAG | 93664 |
rs191439606 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122682119 | CTCCTTAACCTTGTA[A/C/T]TTATGAGACTGAAAG | 93664 |
rs191440299 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122655683 | GACCCACAATATCTC[C/T]AAGGTATGCTTGCAT | 93664 |
rs191440900 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122404141 | ATGCTATCCCTCCCC[C/T]CTCTCCCCACCCCAT | 93664 |
rs191454046 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122629732 | TGCTTTAATAATAAG[A/T]TTGTATTAGTGCTAA | 93664 |
rs191455405 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122578922 | GGATCTGGTGCTAGG[C/G]TGAGAAAAGGGGAAA | 93664 |
rs191456637 | snp | A/G | 0.00164639 | 0.0286441 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698605 | CAACCTCCCCGTTCA[A/G]TAAGTGCAAGCCAGG | 93664 |
rs191457057 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122365532 | AGAAACCCAGTTAAA[C/T]GTTGGGTTTAGTTGC | 93664 |
rs191462095 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122711364 | TCTCAAGATATTTAA[A/T]TATAGATCTACAACT | 93664 |
rs191465448 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122596661 | CATCCCCACTGTAAA[A/C]AACATTGTGCTCTGG | 93664 |
rs191466367 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122684072 | TTATCTTTATTAAAT[A/G]TATAGAGAGCTCACA | 93664 |
rs191471029 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122708256 | CATCATAGGTTCTCA[A/G]TAAAAGTTGAATTAA | 93664 |
rs191471215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122630716 | TATTTTGTTTTCTTT[A/G]AAGATATACACAAAA | 93664 |
rs191473604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122613031 | TTACATTACACCATA[C/T]ACAAAAATCAACCTA | 93664 |
rs191479531 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122493665 | GTTTTACGTACATCA[C/T]AGTACATAGGTACAA | 93664 |
rs191481977 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122764446 | TACAATGTGCCAAGC[A/G]TTTTCCTAGGCATTG | 93664 |
rs191482733 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122469084 | ATTACACATTACAGA[A/G]TATCGTTATAAAGAA | 93664 |
rs191484617 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122511663 | TAGCCATTGAAATCA[C/T]GTAGTTAAATGAGAT | 93664 |
rs191488709 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122491820 | TCTCTAAGAGTAAGA[A/C/T]TAGGAGTAGTCCTAG | 93664 |
rs191489551 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122521364 | GGGACCAAATGCCCT[C/G]AGGCACTTTCAGTCA | 93664 |
rs191491636 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122513427 | AGCCTGCTAAAGGCA[A/C]AGTTTAGCTCATTTG | 93664 |
rs191492353 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122807803 | AGGTGGTCTGTTTCC[A/C]AAGTTTCCTTTTCTT | 93664 |
rs191492744 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122530778 | ATTTTGAAGCAATGG[C/T]TTCCAGCTACCATAT | 93664 |
rs191495790 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122540623 | CTCAGCAATTAAAAC[A/G]GCAAGGCATATTATT | 93664 |
rs191497328 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122558286 | GACAGTCATAATAAT[G/T]AAAATATTTAACAGA | 93664 |
rs191503239 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122430329 | CCCTTTTATATCTTA[A/C]ATCACAATATGCTAT | 93664 |
rs191515180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122449102 | GAGCATGCAAATTTA[C/T]TTATTGTTTAAAACA | 93664 |
rs191522383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122475167 | TTTCAACGCCTGTAG[A/G]CCCTGCGGGTTTATC | 93664 |
rs191526330 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122411553 | AAATATAATAAAAAT[G/T]TATAACTTAAAACAA | 93664 |
rs191533046 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122440339 | ACCCACGATGGGATG[C/T]TGTTCCAAAAAATAA | 93664 |
rs191534937 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122391257 | CACATTTTTAAATTT[C/T]CCCAGAATGGTGAAA | 93664 |
rs191536608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122373542 | AACAGCTGGCCCACA[C/T]AACATTTCTAGCTGG | 93664 |
rs191537391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122415009 | GTCAGAAAACTCTTT[C/T]ATTTTTGTTAACAAA | 93664 |
rs191543464 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122375820 | TCAACATAATGAAAA[A/G]GCAACCTACAAAATG | 93664 |
rs191544700 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122837532 | TTGATAGACCACTAG[C/T]AAGACTAATAAAGAA | 93664 |
rs191548306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122641469 | AATTTTGTAGAGATG[C/T]ATATTTTTTTCCCTT | 93664 |
rs191552094 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | CADPS2 | GRCh38.p7 | 7:122838682 | TCCCATTCACAATTG[A/C]TTCAAAGAGAATAAA | 93664 |
rs191564289 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122857211 | GATAATGATAAGGAT[G/T]AACTGCTCAGCACTC | 93664 |
rs191566375 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122334495 | CTGTGGAAATAGTGA[G/T]TTCTGTCTGTAGGGA | 93664 |
rs191566404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122880584 | TTCTCTTTAGAACAG[C/T]GGTTCTCAACCTTGA | 93664 |
rs191569658 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122877919 | GTGCCTTGTTCACAC[A/G]GTGAGTGAGTGAGAA | 93664 |
rs191583887 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122542856 | TCTTAAATGCATTCC[A/T]TGTTTAATAAACATC | 93664 |
rs191591960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122580784 | GTGATTAATCACAAT[A/G]AACATGAAGAGCAGA | 93664 |
rs191612469 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122442001 | TATACCACAGCAAGA[C/T]TCCAGCTCTTTCCTT | 93664 |
rs191624981 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122503939 | GAGGAAAGAGACATT[A/G]AAAGCATTCTATTTT | 93664 |
rs191631347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122678381 | ACCAACTCACTGAGA[C/T]TGTGCTATAACAATA | 93664 |
rs191633274 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122581459 | GAAGGAAAAGAACAA[C/T]AAGCTTTACAGCTTG | 93664 |
rs191658297 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122616282 | CTCATGTTATGCAGC[A/G]ACCAAAACATCTATC | 93664 |
rs191658625 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122549541 | TGGGAGGACTGCTTA[A/G]GCCTAGGAGGTGGAG | 93664 |
rs191661425 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122568508 | ATATAATATTTACAC[C/G]AAAGAGCTCAATGGG | 93664 |
rs191678328 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122589187 | GTGTATGTTTAATAG[A/T]TGTGTAAAATGTACC | 93664 |
rs191691321 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122697047 | AGTGGGGAGAAACAC[A/G]TGGGAAGTAAATTTG | 93664 |
rs191692626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122377389 | CCCATCTGCCTTCTC[C/T]GTACTCTTCCTTCCC | 93664 |
rs191692915 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122398707 | AGCAGAACTGCAGTC[C/T]AGAACAGCATTATGT | 93664 |
rs191694659 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122357134 | ACTGATATTTCCAAC[C/T]CTAATCCATTACAGG | 93664 |
rs191694827 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122800868 | TGGTGGCACATGCCT[A/G]TAATCCCAGCTACTT | 93664 |
rs191695706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122646200 | TCAGAGCCATGTCTC[A/G]TCCTCATCTTTCATT | 93664 |
rs191696322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122647675 | TTAATCAGATAAAAC[A/G]CATTAAATATCACTG | 93664 |
rs191699608 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122759050 | AATAATGAGCCAAAA[A/T]AATCTTCAGTTTCAG | 93664 |
rs191703735 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122780240 | TTCTGCTTGATTCCA[C/T]TGAAGGTCCTTTACT | 93664 |
rs191704719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122631041 | TAACGTAATTATGAA[A/G]AAAAATAATATGCAG | 93664 |
rs191708374 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817870 | ATTTCCATGCCCCGA[A/C]CTCTTATCTCTGCGC | 93664 |
rs191708893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122804561 | GAAATGTCAAGAATG[C/T]TGGTAGAACTAGAGT | 93664 |
rs191710989 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122360081 | CTCTAATTCTAATTC[C/T]TTGAAAATTGACATA | 93664 |
rs191714219 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122723572 | GGAACACTTTCACAC[C/T]GCTGGTGGGATGGGA | 93664 |
rs191715282 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122613084 | TAAAACTATGAAAGT[C/T]TCAGGAGAAAGCACA | 93664 |
rs191716543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122691821 | TGTCAAGCTGTGCAA[A/G]ACATCCACCCCCAGA | 93664 |
rs191717282 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122860676 | TGCAATAGAATATCA[A/G]GATTTCTCTTATAAA | 93664 |
rs191721290 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122881415 | GAAGGTTAAAAGAAT[A/C]AGCTGAAGCAACAAG | 93664 |
rs191722527 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122676526 | TTGCAATACAATAAG[C/G]TTATGTTCAAGCAGC | 93664 |
rs191726380 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122852700 | TAGCTGGAGCAGAGA[C/G]AGCAAGGGGGAGAGG | 93664 |
rs191731943 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122662469 | CAACCTCCGCCTCCC[A/G]GGTTCAAGCAATTCT | 93664 |
rs191732461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122836127 | GGGGGCCAATATTCA[A/G]CATTCTTAAAGAAAA | 93664 |
rs191742297 | snp | C/G | | | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122701118 | AGCATGGCTAATTCT[C/G]TATGGCAATGTCACA | 93664 |
rs191769897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122739885 | TCGAAGAAACAGACC[A/G]AAATACAATCAGAAA | 93664 |
rs191775266 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122760849 | GATAGCATTTGGAGA[C/T]ATACCTAATGTTAAA | 93664 |
rs191777015 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122460747 | TGGAATCAAACCAAG[A/G]AAGGAAAAAGATATT | 93664 |
rs191777766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122726421 | TCTATCCATTTTTAT[A/G]ACACTGAAAGAGAAA | 93664 |
rs191790895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122393839 | CTGGCAGGTGGTATG[C/T]TTTTATTTTCTAAGA | 93664 |
rs191790913 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122823907 | GTTCCTTGTTTTTTT[A/T]AAAAAAAGCTCACTG | 93664 |
rs191798768 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122571557 | CAAGGCAGACACACC[A/G]AGCAACAACTTTCAA | 93664 |
rs191809003 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122859138 | CTTGGTTTCTTGTTT[C/T]GCTCCTAAAACTGCT | 93664 |
rs191812833 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122424186 | CTCCTAATTCCATGG[C/T]TTCCTTTGGGACCAA | 93664 |
rs191818598 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122472037 | ATCTGGGATATTCTT[A/C]TCATTCTGTTTGTCT | 93664 |
rs191819869 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122355355 | GGATGCCGAGGCAGG[C/T]GGATCACCTGAAGTC | 93664 |
rs191823811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122320556 | TATGACTACATCAAA[A/G]TGTTGTTACTATCAG | 93664 |
rs191824867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122505067 | TCTTTTAAAAATTAT[C/T]GCTTTCTTAAAAACC | 93664 |
rs191831083 | snp | A/C | 0 | 0 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122533080 | TCTAGAGATGTGGGG[A/C]TAAGTAACCCTCAAA | 93664 |
rs191831372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122719757 | TGAAGCTAAAATCTC[A/G]GCAGTATATAAAGAA | 93664 |
rs191835775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122704808 | TTGCCTCTCAGGGGA[C/T]ATCTGGCTGCTTCTG | 93664 |
rs191839404 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122472978 | AAGTTTCAGGTTGAG[A/C]ATCCCAAATCCAAAA | 93664 |
rs191852833 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122453278 | AGTCTAACGCATAAA[C/T]TACAAAGCAGTGCAC | 93664 |
rs191862508 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122434584 | GTGCTGGGAATACAA[C/T]AGTGAACAAGTCAGT | 93664 |
rs191866512 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122517620 | AAATATGTATTTCTG[C/G]TACAACCAAGTTGAA | 93664 |
rs191866996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122664832 | CTCTGTGGCCCAGGC[C/T]GGAGCCCAGTGACAC | 93664 |
rs191872857 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122396055 | CCTCAGGTGATCCAC[C/T]CGCCTCGGCTTCCCA | 93664 |
rs191877572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122415860 | TAGGAGTTATGTTTT[C/T]AGAAAATTCACATAT | 93664 |
rs191881011 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122693589 | CATCCTGAACACTGA[C/G]ACTTGGAAAAGCTCT | 93664 |
rs191881667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554276 | TCAGTGCCCTGGTGC[C/T]CTGTATCAATATGAC | 93664 |
rs191893717 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122633309 | GTTTAATGATACTGA[G/T]TTTTCCATTCCATGA | 93664 |
rs191898898 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122497429 | AATCTCCCTATTTCC[G/T]CAACAGTATAGAAAC | 93664 |
rs191900099 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122665912 | TAAGTGACAGGTATA[C/T]GCATAGTGCTTTAAA | 93664 |
rs191920856 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122721511 | TTGAATCTCTGAATA[A/G]ACCAATAACAGGCTC | 93664 |
rs191928829 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122640858 | AGAATGGCGTGAACC[C/T]GGGAGGTGGAGTTTG | 93664 |
rs191935916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122598369 | CTTACATTTAAAAAG[C/T]AGTTTCTCCAAGAAA | 93664 |
rs191947172 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122607011 | CCTGATATGACAAAC[A/G]GCATTTGCTAACCAA | 93664 |
rs191964942 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122605264 | TGCACACTACTACAG[A/T]CTTTATAAAAACTGA | 93664 |
rs191967694 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122669959 | TCCTGACTCCTCACA[A/T]CCTCCACGTTATATT | 93664 |
rs191972446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122655164 | TAATCCTAGTGAAGA[C/T]GCTGTGAACACTGTT | 93664 |
rs191974219 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122455549 | CACCAGATGGCATAT[A/T]GTTGATATTTAATGC | 93664 |
rs191975038 | snp | A/C | 0.311614 | 0.242289 | intron-variant | CADPS2 | GRCh38.p7 | 7:122819668 | GTTATCCCCACCTGC[A/C]CAGTTCCCTTATTAG | 93664 |
rs191976776 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122621927 | TTATTGAGGATCACT[A/G]CAGTACAAAATGAAA | 93664 |
rs191978803 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122561586 | GGGCATTAGGCAAGC[C/T]GTTAGTAGTCTACGC | 93664 |
rs191981292 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122855485 | CCCAAGAAAATTCTA[A/C]GGGCAATTTAAAAAA | 93664 |
rs191981531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122419279 | CATCTGTATCTAATA[C/T]ATCAAGGGTGGATAA | 93664 |
rs191984515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122782497 | ATGTCTGCGGTCCCA[A/G]CTACTCAGGATGCTA | 93664 |
rs191985620 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122639737 | AATAAATTATACTAA[C/G]CCAAATATGATTTTC | 93664 |
rs191992354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122720474 | TATATGTAGATATAT[A/G]TATGTATGTATATAT | 93664 |
rs191999470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122379953 | CAGCAGTTTATACAA[C/T]TCTTACAATATGCTC | 93664 |
rs192000420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122692155 | CAGGTTGTACACCAA[C/T]GTCCTTCTCCTGAAT | 93664 |
rs192002295 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122705055 | TCAGGTATAAATTCT[C/T]GACACAAAATAAGCT | 93664 |
rs192014223 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122338885 | CTCGCCTTAGCCTCC[A/G]AAGTAGCTAGGACTA | 93664 |
rs192017156 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122348525 | AGTGTTTCCTTTTTT[A/T]AAAAAAATTGCATTT | 93664 |
rs192018156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122752739 | TGTGAAACTTCCTAC[A/G]ACAGGTTAATATATA | 93664 |
rs192026035 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122782631 | CAACAACAACAACAA[A/C]AAAAAATTGAGTTTT | 93664 |
rs192041256 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122714381 | ATTGTTTCTAGCTGT[C/T]TTTAGTATTTAGCTT | 93664 |
rs192052764 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122596547 | GCGTGAAATGTAAAC[A/C]AATACTATAGCAGTG | 93664 |
rs192064204 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | CADPS2 | GRCh38.p7 | 7:122741387 | TCAACATTAGCACTT[C/T]ATTCATTTTGAGTTT | 93664 |
rs192073960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122557980 | CAAGTTCAGAGAACA[C/T]CAATACCTAGGAAAC | 93664 |
rs192087344 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122404505 | TTCTTTGGGTATATA[C/T]CCAGTAATGCGATTG | 93664 |
rs192088649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2, LOC105375481 | GRCh38.p7 | 7:122530012 | TCTATAAGACATATT[C/T]TGGAATTAGTGCTAT | 93664 |
rs192091061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122426203 | GTCAAAAGATCTCAA[C/T]GTCTGCATGTATGTC | 93664 |
rs192094720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122552600 | AGTATGCTAAACCAA[A/G]GAACTGCCAGGTAAG | 93664 |
rs192095214 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122386613 | TCAACCTAAATTTTT[A/T]AAAATGGAAGCTACT | 93664 |
rs192103050 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122591281 | ATCCAACTTATAAGG[A/G]ATGTGAAGGAACTCT | 93664 |
rs192112503 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | CADPS2 | GRCh38.p7 | 7:122366474 | CCCGGCCATGGTGGC[A/G]GGCGCCTGAAATCCC | 93664 |
rs192113267 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122516035 | TGGTTTCTTTGAAGA[C/G]AGAAAGCAGGGGGAC | 93664 |
rs192116678 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122346049 | CAATTTACTTTGCAT[A/C]ATCTCTGGCTGGCTT | 93664 |
rs192121007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122731982 | TTAAGACATCTTATT[A/G]AAAATATGATATAAA | 93664 |
rs192124995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817545 | AATCATTGCAGGGAC[A/G]CCTCTCTGATTATTC | 93664 |
rs192125039 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122768070 | TTGTCAATCACAAAA[C/T]AACAAAGTAAAATGT | 93664 |
rs192126618 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122545560 | AATTTTTTTTTTAGT[A/G]GAGATATAATTGTAT | 93664 |
rs192128206 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122489591 | TTAAGGTACAAGGGG[A/G]AAAAAGTTGGCTTTA | 93664 |
rs192128966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122321367 | GAGACAAGGTCTTGC[C/T]ATGTAGCATAGGCTT | 93664 |
rs192130143 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122562981 | CAAGTTCCACACAAC[C/G]TAACGATTAAGAATT | 93664 |
rs192132845 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122750486 | TGGATTGTCCTGTTT[C/T]TATGCCCAGTTATAA | 93664 |
rs192134681 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122586088 | ATGAACTATTTTGCT[A/T]CTTTATAATGATGGC | 93664 |
rs192135613 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122486401 | GATAACTTTAAGGGA[C/T]TGAAGACTTGAGTGG | 93664 |
rs192139173 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122788422 | TTAACTTTGTAGTTT[G/T]CAAGCAAACAGGACC | 93664 |
rs192142535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122688697 | GCAGGGCAATGATAC[C/T]TTTTACAAACAATAG | 93664 |
rs192143868 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122452168 | ATTAAAAATGTAAAA[C/T]ATATCAAATAACAGA | 93664 |
rs192146921 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122506390 | CAGACTTTAATCTGG[A/G]GACAGAATTAAATCA | 93664 |
rs192153049 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122809705 | ATAAGAAGTCAAATA[C/T]TAACAACTCCTGTGG | 93664 |
rs192181460 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122715226 | CTGAGTTTTCATACC[A/G]ATATACAGGAGTTAT | 93664 |
rs192188461 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122487792 | TCCATCTCTGGAGGA[C/G]TGAATAGAAATAAAA | 93664 |
rs192194730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122453518 | TAAATTACATTATCA[C/T]GTAGACAACAATGAA | 93664 |
rs192196853 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122473118 | AAGGTTTCTCTATAC[A/T]TTGTGAATTATAAAC | 93664 |
rs192201541 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122679180 | ATTTCTCTTATTACC[A/G]AAAACAGGTAAGATA | 93664 |
rs192202463 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122658572 | AAAAAAGGATGAGTT[A/C]ATGTCCTTTGTAGGG | 93664 |
rs192217185 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122734067 | ATTCTTATTCAACAG[G/T]TCTTGTATGGAACCT | 93664 |
rs192229676 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122448815 | GAAACTTTTTATGAT[A/C]TTAAGAGAAGACTAT | 93664 |
rs192234862 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122847387 | CCACCGTGCCCAGCC[A/G]GTATTCATCTCTTCT | 93664 |
rs192240712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122410375 | AAAAACAAAAACAAA[A/G]CTTATACAGGATTAA | 93664 |
rs192259713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122372690 | ATTTTCATCTACTTT[A/G]TGTTGAGTTAATTAT | 93664 |
rs192260998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122753776 | ATATAAACACACGAA[C/T]GCTTGCATGCTCTTG | 93664 |
rs192274524 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122773825 | AAGCTTTCCTTAAAT[A/T]ACCTTTCACATTTTA | 93664 |
rs192274882 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122734619 | AAATAAAACATAAAG[A/G]TCATGATCACAGGAA | 93664 |
rs192275281 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122624935 | AAAGTCTAGAAGGAG[C/G]AACACAGAGTGAGTG | 93664 |
rs192276120 | snp | C/T | 0.00599571 | 0.0544234 | intron-variant, synonymous-codon | CADPS2, RNF148 | GRCh38.p7 | 7:122702589 | ACTCTCTCCTAATTC[C/T]GATGTGATCTCATTT | 93664 |
rs192287248 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122341051 | ATGTGCCTCAGTGGT[C/T]ACGTGAGAGGCAGAG | 93664 |
rs192288298 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122795289 | ATATTACCACTGACC[A/C]CATAGAAATACAAAC | 93664 |
rs192293036 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122436483 | TTTGATTTGGTTCTT[A/T]GTCTAGTCCTGAGGA | 93664 |
rs192297555 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122776178 | CCTGGAGCAAGGTAA[A/T]AAAATCATGTGGGGC | 93664 |
rs192300649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122813934 | GAGTGAAAGTTTTAA[A/G]GTAATATTGACTATC | 93664 |
rs192306690 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122815464 | ATTTGTAACAAAAGA[A/C/T]CAAAACATTAACCCT | 93664 |
rs192313319 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122837060 | AAATGTAAAAGAACA[C/G/T]AAATTATAACAAACT | 93664 |
rs192320648 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122876360 | CCAGCAAATCTAATT[A/T]TATATTTATTTTTTC | 93664 |
rs192322086 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122589980 | AAATGCATGCAATCA[C/T]GTATACAGAACTTAT | 93664 |
rs192326440 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122689348 | ATGTCTAAGGCCATC[C/T]GGTTTTGTAGCACCA | 93664 |
rs192327352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122399275 | ATCAAGTTATTTGTG[C/T]ATATATGTGCGTATC | 93664 |
rs192329537 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122706348 | TATTCAAGGAATATA[C/T]ATATATGCTTATATA | 93664 |
rs192336415 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122721872 | TTCATCCCTGGGATA[C/G]AAGGCTGGTTCAATA | 93664 |
rs192343635 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122623453 | CCATCCAATGATCAT[C/T]TGGGGAAAAGTTCTT | 93664 |
rs192345969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122659217 | ATTAATAGGCTAAGG[A/G]CCCTAATGTAAAAAG | 93664 |
rs192351845 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122883528 | TGTTACTTCTTTTAG[A/T]TAATCTAACTGTATA | 93664 |
rs192353039 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122551386 | ACACTGTGGGAGGCA[C/T]TGAGAATTCAAATAG | 93664 |
rs192353621 | snp | G/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122478722 | ATGTGAGGACTATCA[G/T]TGAGGGGCTTTTTGG | 93664 |
rs192355661 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122370060 | GCAGTTTCTCTTACT[C/T]AAATGGTCCTTTCAT | 93664 |
rs192359730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122646871 | GAGATAATGAAGTCT[C/T]CAGCTATGGCAATTG | 93664 |
rs192362679 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122517025 | TCCACCTCCCCAAAA[A/G]TTCCCTTATGCCCTT | 93664 |
rs192370031 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122496698 | TAAATTAATTTCATT[C/G]TTATCAGAATAATTC | 93664 |
rs192374581 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122324689 | AATGAAAGTAAAGGT[C/G]TTTTGTTTAAATAAA | 93664 |
rs192380686 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122464436 | GAATAACGTATGCAG[A/C]TAGTTCTCCTTCTAG | 93664 |
rs192384780 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122426623 | TACAGAGGTAGAAAC[A/C]TGTCAGTTTTCATCA | 93664 |
rs192389823 | snp | A/C/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122804866 | TTGCTATTTCTAATA[A/C/T]CATATACTTAAAAAT | 93664 |
rs192390634 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122376849 | TACAAACTCATCTTG[C/T]ATATATTAAGCATGT | 93664 |
rs192395153 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122483224 | AAATTGCTCAAAAAC[A/T]GTGTTAAAGAGAAAA | 93664 |
rs192396075 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122355658 | CAGAAAATTTTTTCT[A/G]GCTCTTTATCTTCTC | 93664 |
rs192398180 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122636275 | TCTTTTAAGGACCTC[C/T]TGTAAGGGTAGTCTA | 93664 |
rs192404019 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122404921 | AGGAGGTCAGGAGAT[C/T]GAGACCATCCCTGGC | 93664 |
rs192405718 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122577603 | TTTAGTGATTAAGAA[A/T]AAAGCTGTTTAAACA | 93664 |
rs192415495 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122810162 | ATGTTGTACCAAGTA[A/G]TGGCTTTGCTTCACC | 93664 |
rs192419960 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | CADPS2, RNF148 | GRCh38.p7 | 7:122701382 | ACTCATAGGTGGGAA[G/T]TGAACAATGAGAACA | 93664 |
rs192420581 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122611958 | AATAAAAGACAAAAT[A/C]CACATGATCATCTCA | 93664 |
rs192423108 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122827314 | TCCAAAAAAGAAAAT[C/G]TCCAGCCCTAGATGG | 93664 |
rs192426740 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122841533 | GATAAATTTTAAAAC[C/G]AACTTATCAAAGTAG | 93664 |
rs192429227 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122600945 | GTTATTTAACATTAA[C/T]GTAGATGTTGACATT | 93664 |
rs192431057 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122861951 | CCTGGAATTCTATGC[A/G]CAGCCAATTTCCCTG | 93664 |
rs192432069 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122667524 | CAACAACATTTCAGG[A/G]ATTCTGCTAAGTGTT | 93664 |
rs192435568 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122618395 | GCAACTTATATTCTA[A/G]TAGAGAAAGCCAGCT | 93664 |
rs192435731 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122688308 | CAAAGAACATATTAT[C/T]TTGTAGGCGACCCAC | 93664 |
rs192435756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122651418 | GGGGAAGACACCCAC[A/G]GTGACCACAGCAACT | 93664 |
rs192441166 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122673193 | AACAGCAGCAAGATT[C/T]ATTGCAAAGAGCGAA | 93664 |
rs192454324 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122546498 | TAGGCCATGTCCTAT[C/G]CTTTGCTATGTTCCA | 93664 |
rs192460717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122563321 | TACTGCTTGAGTAGC[C/T]TTATCATTTTTCTTT | 93664 |
rs192460816 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122586508 | TATTTATAAAATTAT[A/C]TAAACTTGGGTTTGG | 93664 |
rs192465399 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122510573 | ATGGTTGGATTTCCA[A/G]TGATATCACTCATAA | 93664 |
rs192466540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122799864 | TCAGTCAACACATCT[A/G]TCGGCATTGAGGAAA | 93664 |
rs192483849 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122676005 | AACAACAACAAAAAA[A/C]GAAATTATAACCTCT | 93664 |
rs192489872 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122474640 | TTATCACATGAAATA[G/T]GATGCCAAGAGTTCA | 93664 |
rs192515188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122704455 | ACATCATCATATTAG[A/G]GGTAATTTGTTAAAT | 93664 |
rs192518880 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122362714 | AAATTAACGAAGACT[G/T]GTTTTTGTTCACATA | 93664 |
rs192520472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122796264 | AGGAAGACTCAATAT[C/T]GTTAAATTGGCCATA | 93664 |
rs192523053 | snp | A/G | 3.31241e-05 | 0.00406952 | intron-variant, synonymous-codon | CADPS2, RNF148 | GRCh38.p7 | 7:122702256 | TCCTTTCTGAATCGA[A/G]TGCAAAATTTCCATG | 93664 |
rs192525293 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122409120 | TTTTTGGTTAAATAT[A/G]TGATAAAATGGGTAT | 93664 |
rs192530005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122814593 | TATTGGAACACAGCC[A/G]TACTCATTCATTTGT | 93664 |
rs192531689 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122342380 | AACCAAATCCTGGGG[C/T]ATTTCATCACAAAAA | 93664 |
rs192541167 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122673765 | GCCTAGTGGATCCCA[A/C]ACCAGGGCTGCAGGC | 93664 |
rs192544446 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122847147 | GCTGGAGTGCAGTGG[C/T]GCAATCTCAGCTCAC | 93664 |
rs192547607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122833266 | GTTTTAAGTACTACT[A/G]AAATTGACCATTTTT | 93664 |
rs192549622 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122726885 | AAGCTGACAAGATAA[A/G]GTAAAATGAATAAAA | 93664 |
rs192556936 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122868081 | TCTTCTCTGACTTGC[G/T]TCAGCAATAAATCTA | 93664 |
rs192558666 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122741805 | TCCCTATGGCTTCCA[C/T]ACAACTCTAGTACTA | 93664 |
rs192562159 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122437338 | AGGAGGTTGGTTATC[C/G]TATGCTTGTTAGAAA | 93664 |
rs192571792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122714949 | GTGTAATTGGTTAAA[C/T]GTCATACAGCTATAA | 93664 |
rs192575665 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122726718 | CTCTTAAAAACTTTT[A/T]AAAAAGAACATAAAA | 93664 |
rs192579570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122805288 | CCTCAGCCTCCCTAG[C/T]AGCTGGGACTACAGG | 93664 |
rs192583766 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122865577 | ACTTCTGTACAAACA[C/T]TGCCTCTGCAATTCC | 93664 |
rs192596310 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122400347 | GAGGCTGAGGCAGGA[A/G]AATTGCTTGAATCTG | 93664 |
rs192604338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122362085 | AAAAGAAAAACAAAA[A/G]CAAAAACAAAAAACC | 93664 |
rs192610000 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122618068 | AAAAATCAACTATAT[G/T]CATGCCACTGATAAC | 93664 |
rs192620992 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122568934 | ATATCATATTGAATG[C/G]GCAAAAACTGGAAGC | 93664 |
rs192626352 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122589405 | TGTACAAATGTTTTT[A/T]AAAATAGCTTTCTTC | 93664 |
rs192633831 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122833744 | AGTGGTTAAGTAACA[A/T]AATATTCTTAAAAGG | 93664 |
rs192644548 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122482836 | GCTGCCCAGCAAGAG[A/C]CTCTCAAGATCTACA | 93664 |
rs192654176 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122429963 | TACTTATTGCTATCG[G/T]GTACAATGGAGTGTT | 93664 |
rs192655600 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122390244 | TAAATAAGAGAACTA[C/G]ACAACACCATTCTGA | 93664 |
rs192657460 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122869559 | TCATCACCACTAGAC[A/C]TGCTTTACAAAAAAA | 93664 |
rs192661699 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122456434 | TGGGGCCTGTAGTTA[C/T]TGAAGTTACATGATT | 93664 |
rs192667223 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122501151 | TCCCAGCTACTTGGG[A/T]GGATAAGGTGGGAGG | 93664 |
rs192671902 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122604520 | GCATCTTAGAATAAA[C/G]GCATTTCTTCTGACT | 93664 |
rs192673277 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122579210 | AGGCAGGGTTGATTT[G/T]GCACTACCCTCCAGG | 93664 |
rs192676503 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122447962 | GCATGTCTAAAAATA[C/T]CATTATTCTACCATC | 93664 |
rs192680141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122401540 | AACAACTATGGAAAT[A/G]GTGTGCAAGGGTAGA | 93664 |
rs192684675 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122467762 | CTGACTTACAAAACC[A/C]AGACGTATAACCACA | 93664 |
rs192687573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122422153 | GAAAATGGGAAAATA[C/T]CTACTATCTAGTGAA | 93664 |
rs192688119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122754349 | CTTGAAGGAATTTGA[C/T]AAATAAGTTAGAAAA | 93664 |
rs192692498 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122429120 | CTGTTATAAACTTGA[C/T]AGCTTCTCAATACTT | 93664 |
rs192696131 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122502729 | AAAATAAACCATATG[C/T]GTTTATTTCATTATT | 93664 |
rs192699313 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122381919 | TGGGATTCTGCTATT[A/G]TAAATGTATCTGGTT | 93664 |
rs192705857 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122541134 | GGTTCAGAATGAAAT[A/G]GAAAAAGCAGCACTT | 93664 |
rs192711669 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122796477 | CTATACTACAGGGCT[A/C]CAGTAACCAAAACAG | 93664 |
rs192719217 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122825147 | GGAGGTTGTCTAGCC[A/C]TAACAGATATTAAAT | 93664 |
rs192720372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122605960 | AGCAATGTCCATCAA[C/T]TTAATTCCTGCCTAT | 93664 |
rs192723466 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122661611 | GACATATAAAGAGCT[C/T]GAAAGTCATCACTCC | 93664 |
rs192726385 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122531985 | GCAGTGAGCCAAGAT[C/G]GTGCCATTGCACTCC | 93664 |
rs192735350 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122699425 | GTGAAGGAGATATTT[C/G]CAACAAAATGGCAAG | 93664 |
rs192740583 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | CADPS2 | GRCh38.p7 | 7:122570777 | TCTCAGTAAACTATC[A/G]CAAGGACAAAAAACC | 93664 |
rs192743504 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122725799 | ACCATGGTCTTGCCT[A/C]ACATGTAGGTTACAA | 93664 |
rs192749649 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122787116 | AGAAGGAATACAAAC[A/T]TTAAGCAATGAGGAA | 93664 |
rs192752341 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122749038 | TCTAGTTTACTGCCT[C/T]CAAAGAAATCCACAT | 93664 |
rs192756403 | snp | A/G | 0 | 0 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122562292 | GGTGGGCCCAATACA[A/G]TCACAAGGGTTCTGA | 93664 |
rs192761003 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122468815 | AAACGTCACAGGAAA[C/T]GTCATAACTTTCAGC | 93664 |
rs192761389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122501964 | GGATATTCTTTCCAA[C/T]ATATCATATTATTTT | 93664 |
rs192764656 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122599795 | AATATGAAATATACA[C/T]ACATATAGGATACAG | 93664 |
rs192768882 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122525287 | CAGAGCTCTGAAATT[G/T]AGTAAACAAACTATG | 93664 |
rs192773906 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122465141 | GAAGGTAAAAATGAA[C/G/T]AATATTAGACTGAGG | 93664 |
rs192778585 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122778947 | GGAGGGACCTGGTAG[A/G]AAGTAATTGAATCAT | 93664 |
rs192787425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122487615 | CAATAGCAAGGAAAG[C/T]ATGAAAGGCTTAGAA | 93664 |
rs192791267 | snp | G/T | 0.0659589 | 0.169201 | intron-variant | CADPS2 | GRCh38.p7 | 7:122427146 | TGTGTGTGTGTGTTT[G/T]AACTTTTTCTTTTTT | 93664 |
rs192795729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122691436 | ATTTGTGGTCACATG[C/T]ACATTCAGTTTAAAT | 93664 |
rs192799905 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122640027 | TTGAAATTAACAAGC[C/T]CAGAATAGAATCTCA | 93664 |
rs192808915 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122710960 | CAAGGTCCCTGACAA[A/G]ATGTTGATTTTCAAG | 93664 |
rs192810702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122662762 | AAATTACATAGTTCA[A/G]CTATCATCCTCAATT | 93664 |
rs192814615 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122683815 | TGTTCTCCCCAAGTC[C/T]ACATGGGTTTCCTCC | 93664 |
rs192825454 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122483369 | CTTAAAGTACTAAAA[G/T]AAAAATATCTTCAAA | 93664 |
rs192828046 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122738325 | CCCTTCTAGGCACTA[A/G]GCCCTGCACAACTGT | 93664 |
rs192837832 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122458285 | GGAAAGGAGAGGATG[A/T]CACAGCACGAGAATA | 93664 |
rs192839957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122421879 | TTCAGAATGAAATTA[C/T]TGTGGTGGGTATGTG | 93664 |
rs192844411 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122846368 | ACTGTAAATACTTTA[C/G]AAATTTTGCAAGTTT | 93664 |
rs192845942 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122632110 | CAACCCACCATTAAT[A/G]GGCACCTATGTTAAT | 93664 |
rs192848449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122820326 | CTTCAATCAAGCCCA[A/G]ATTTCTTCCTCATCT | 93664 |
rs192853163 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122597413 | AATGTATGTGTCCCC[A/C]TACAGTGTACATGTT | 93664 |
rs192853754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122381688 | CCTATAATACACTCC[C/T]GTAGATTGTTGCTTG | 93664 |
rs192856086 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122416775 | TCTTTGAAGCTGAAG[G/T]TTCTTTCTGCAGTAA | 93664 |
rs192858854 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122341457 | CATCTTTAGTTTACA[A/C/T]GTACTAAGTAAACTG | 93664 |
rs192859418 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122839741 | TGAGATACCATCTCA[A/C]ACCAGTTAGAATGGC | 93664 |
rs192860450 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122478429 | AATTGAGGATACTGG[C/T]GGAGTTTCTATGGCA | 93664 |
rs192863364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122882825 | ATCAGGGTAAATCAG[C/T]ATTAGAGGCTCAAGC | 93664 |
rs192864411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122443254 | AATTCAACACATTTA[C/T]GGAGTACAAGTAATC | 93664 |
rs192867457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122377779 | ATCCACTTGTTGGTG[A/G]GTGTGTGAGGTATCT | 93664 |
rs192875776 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122337366 | GGAATGTGCCAAATG[A/T]CAATTGTGTTCCACG | 93664 |
rs192881761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122778615 | CCTAGGGACTTGGTG[C/T]CCTGTGTCCCAGCTG | 93664 |
rs192890320 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122559684 | GCTGAGACAGGAGAA[C/T]AGCTTGAACCCAGGA | 93664 |
rs192899351 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122597146 | CATTTGGCCCCACCT[A/C]CAACACTGGAGATTA | 93664 |
rs192901455 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122522225 | ATTCAAGAGATTCTC[A/G]TGCTTCAGCCTCTTG | 93664 |
rs192908151 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122618243 | CCTAAAAGTAATCCT[C/G]AACGGCTGTTTTTTT | 93664 |
rs192913789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122809098 | TTATGCTTCATATCT[A/G]CTTCATGTGGTTTTC | 93664 |
rs192926401 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122336221 | AGCCAACACTGGTGA[A/C]CTGGCTGCCACTGCT | 93664 |
rs192928433 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122839607 | AAACAACCCCATCAA[A/C]AAGTGGGCAAAGGAT | 93664 |
rs192932724 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122553919 | TTTGGCAATTCATTT[C/T]ATTCAAGAGTTCAGA | 93664 |
rs192943681 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | CADPS2 | GRCh38.p7 | 7:122731244 | AGCCAAGTCACAAAT[A/T]TTTTTTTTTTTTAAG | 93664 |
rs192951426 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122516925 | GTATAGTTTACATAA[A/C]GTAAAATTACCTGTT | 93664 |
rs192956110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122712148 | CTAGTGTTGAAAACA[A/G]TGTTACTTTTTCCCC | 93664 |
rs192956387 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122727740 | GAACACACTCACAGG[A/C]AGCAGAAACCCAGAT | 93664 |
rs192961105 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122767047 | TACAAAAATCATTGT[A/G]TCCTAAAACAATAGT | 93664 |
rs192970247 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122584795 | TTAGAATTTCTCTCT[A/C]TATATATCTTTTCCT | 93664 |
rs192973843 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122832267 | TTAGGTAAAACAGAG[A/G]AAAAAAACTGGAGAT | 93664 |
rs192975507 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122479175 | GGTGCTGCCAGCCAA[C/G]ACTGCTCTCTGCAAA | 93664 |
rs192976953 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122762925 | AAAGATAGGAGGTCA[C/T]TGGGAACAGGGAAAA | 93664 |
rs192977585 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122505963 | ATAGTACTAACACCT[A/G]TAGCTGCTGGTTTAC | 93664 |
rs192981537 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122544541 | TGTGGTCAGTTTCAC[A/G/T]CTGGCTAGCTGGCTT | 93664 |
rs192989053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122650861 | ATCCAATTTACATTA[C/T]GATACATTTATTTAC | 93664 |
rs192989817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122444782 | TGTCTTTGGAAGATC[A/G]AAAGTTCTCAATTTT | 93664 |
rs193016372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122676817 | AAGATTCCGAACTCA[C/T]TGTAAGTGCTTGGTG | 93664 |
rs193023179 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122647893 | TGTATAGAAGGAATT[C/T]ATTGAATATATAATG | 93664 |
rs193027761 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122757456 | ACCAGCCAGGAATGT[G/T]TTTTAAAGCATTCTG | 93664 |
rs193028486 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122434417 | AACTTGCTTATAACA[C/T]TGCATACAAAATTTG | 93664 |
rs193029305 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122835843 | GAATGGAACCAAGTT[G/T]GAAAACACTCTGAAG | 93664 |
rs193032218 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122724727 | GAACAAAACTCGCAA[C/T]GTTTTTTCACCTTTT | 93664 |
rs193037704 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122368490 | CTTGGGCCTCTGTTT[C/G]CTCATCTGTGAACAG | 93664 |
rs193039138 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122613456 | ATATATATGGAAGAT[A/G]TTTATACCATATCAG | 93664 |
rs193039873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122873530 | GCTGCATAGTATTCC[A/G]TGGTGTATATGTGCC | 93664 |
rs193044592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122394918 | CAATAGACTAGGTAA[A/G]GGATGATAATGGCTT | 93664 |
rs193046624 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122321850 | TGACTGGTATTTTAT[C/T]ACTACTGATTTTTAA | 93664 |
rs193061242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122463551 | ATAAGACATTTCTAT[A/G]TGTAGTAAAAACAGA | 93664 |
rs193065156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122435418 | GGTGCTCAACATCAC[C/T]AATCTTCAGGGAAAT | 93664 |
rs193066051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122396393 | TTAATGCAATAATAA[C/T]CTAACTGGTCTTTAG | 93664 |
rs193069122 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122861419 | TTTGAGAAATGTCTA[C/T]TCAGATTGCTTGCCC | 93664 |
rs193075706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122357583 | GTATCTACCATTACA[A/G]TATCATACAGAATAG | 93664 |
rs193085286 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | CADPS2 | GRCh38.p7 | 7:122608036 | ATCCTGGCCAACACA[A/G]TGAAACCCTGACTCT | 93664 |
rs193093662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122535729 | ATAGATCTTGTTTTA[A/G]AGCCTAATGGCAAGA | 93664 |
rs193095561 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122573698 | CAAACTAAATAGTTA[A/C]CAGGAATATATTACA | 93664 |
rs193098247 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122389498 | CATGTATGAAGATAA[A/C/T]TTATAGAAGAGTTAC | 93664 |
rs193103732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122351935 | TATCAATGGGGAAAA[C/T]CCTTTCAAAGAGAAG | 93664 |
rs193108719 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122799463 | ACAAAATTAGCCGGG[C/T]GTGGTGGTGGGCGCC | 93664 |
rs193117011 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122695342 | ACATTATTAGTCCCA[A/T]GTCATTATGACAAGA | 93664 |
rs193119550 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122753887 | TGCAGGTCACCAAAA[A/C]CTTTTTTTTTTCCCT | 93664 |
rs193122863 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122721989 | GTTAACAAAATTCAA[C/T]AACCCTTCATGCTAA | 93664 |
rs193134127 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122492973 | GAAACTAAGGAAACA[C/T]AGTACCTTTCAATAG | 93664 |
rs193136696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122531427 | TAAAACCAGAGGTTT[A/G]AAGTTCTTCTCTTAA | 93664 |
rs193138518 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122458646 | TTTAAAAAGGGTAGA[C/T]ACCACTATGGTGAAA | 93664 |
rs193139822 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122857763 | TTCTTCCTTCTGGTG[A/G]GTTCGTGGTCTCGCT | 93664 |
rs193148464 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122825978 | CCAAGTAGCAAGCTA[A/C]AACTATGGTGCACAC | 93664 |
rs193155170 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122600703 | ATGACATGAGTTTGT[G/T]CAGAGCTGAACTTAA | 93664 |
rs193162390 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122635224 | TGCCTGGATGATCTA[A/G]TGCTGTCAGTGGGGT | 93664 |
rs193168809 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122534061 | AACTCCTTTATTATC[A/C]TCATTATATAATATT | 93664 |
rs193174856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122496144 | CTTATCTCTTCATTT[A/G]GGATATTTATCTCTT | 93664 |
rs193184567 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122715919 | ATTCAATATGAAAAC[A/T]CTAAAGGTATTTTTT | 93664 |
rs193189761 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122744124 | TATGCCTGACTTCCA[G/T]GAAACTGTAACAGGT | 93664 |
rs193190011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122783466 | CAACTGTGGTAGCAC[C/T]CCTCTCACAGGAGCA | 93664 |
rs193195951 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122666680 | TCGGTAGAGGCTGCC[A/G]GAGGACGTACACTGG | 93664 |
rs193201759 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122694955 | CCAGTTGATACCTAC[A/G]TGCTGCTTCAAAACC | 93664 |
rs193218134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817746 | CTCCTTCACTCTTAG[C/T]GGCAAGTCCTGCTTT | 93664 |
rs193219672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122415373 | GACGGGTTTGTGTTC[C/T]GTCTTTGCCTCTTAC | 93664 |
rs193221433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122386786 | ACAACACTTCAGCTG[C/T]TAAAAGCTATATCTA | 93664 |
rs193225183 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122346146 | CTGAGGCAGGTGGAT[C/T]GCTTGGGCCCAGGAG | 93664 |
rs193230689 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122657540 | ATCCCTTGTAAGTTG[C/G]ATTCCTAGGTATTTT | 93664 |
rs193236230 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122680532 | CAGCCTGGCCAACAT[A/G]GCAAAAGCCTGTCTC | 93664 |
rs193243220 | snp | A/C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122593085 | ATAATATACTGCATG[A/C/T]AATACAGTGAGGACA | 93664 |
rs193247232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122626199 | TTTTTCTCAGCAACA[C/T]AGGGAATCATCACAG | 93664 |
rs193251521 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554080 | TTGATTCAATTCTCA[C/T]TCACATGTTTGGATC | 93664 |
rs193256174 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122775049 | ATACAAAATTAACCT[A/T]CTTCTAGAAGTTTTC | 93664 |
rs193259053 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122372546 | GATCTAAAGGTAGCC[C/T]TGAAGAGGAGAGGTA | 93664 |
rs193263385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122327966 | TCTATCAAATAAGAA[C/T]GTATATTTTGGCTCC | 93664 |
rs193265884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122706938 | AAATCCTTGGAAACC[A/G]GAGTGGAATCATCAT | 93664 |
rs193277951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122735303 | ACAACACCATAAACC[A/G]AATCTGTCTACAGGC | 93664 |
rs193280973 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122550701 | TAATACTGTTACTTA[C/G]CCACTAGGCTATGCT | 93664 |
rs193289074 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122512431 | GGATTTATCATGGAC[G/T]GGAATGACTATTACT | 93664 |
rs193294374 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122475451 | TCTGGTCATCATAAG[A/T]AAAGCAGAGTCCTAA | 93664 |
rs193294553 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122437684 | TACTTTTAATTACAT[A/G]AATTAATGTGTTGAA | 93664 |
rs193296173 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122878375 | GCAATGTTGTCGGCC[A/G]GGCGCGGTGGCTCAC | 93664 |
rs199505684 | in-del | -/AA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122361247 | TTTTTTTTTTTTTTT[-/AA]AATGAGATGGAGGCT | 93664 |
rs199514313 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122477054 | AGAGGAGAGAGAGAA[-/G]AGAGAGAGAGAGAGA | 93664 |
rs199521819 | in-del | -/AT | 0.0150606 | 0.0854603 | intron-variant | CADPS2 | GRCh38.p7 | 7:122617694 | CATATAGCACCAAAC[-/AT]AGAGAAAGTCATGGG | 93664 |
rs199522407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122649380 | CTCTATTTCCTGGCA[C/T]CCAACTAGACTGTTC | 93664 |
rs199525196 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122373859 | TCTTTAAACACTACC[-/A]AAAAAAACCCCAAAA | 93664 |
rs199528848 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122709363 | CACAATGAGATACCA[C/T]CTTACACCAGTTAGA | 93664 |
rs199530589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122860060 | TTCTGGGATTTATAA[A/G]TGCACTAATAAAAAC | 93664 |
rs199542036 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122762015 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 93664 |
rs199555538 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122723143 | TTCATGTCTAAAACA[A/C]CAAAAGCAATGGCAA | 93664 |
rs199561782 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122421783 | CAGTATGTAAGAACA[-/G]GGTTATTAGCTTGCA | 93664 |
rs199564848 | in-del | -/TC | 0.181022 | 0.240296 | intron-variant | CADPS2 | GRCh38.p7 | 7:122679725 | TCCAGCTTTAAAATT[-/TC]TCTCTTTTGTACTCT | 93664 |
rs199579125 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122437337 | CAGGAGGTTGGTTAT[C/T]GTATGCTTGTTAGAA | 93664 |
rs199582659 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122619635 | CAGTCTCCAAACAAA[C/G/T]AAATAAATAAGATAA | 93664 |
rs199606062 | in-del | -/TTT | 0.139564 | 0.224285 | intron-variant | CADPS2 | GRCh38.p7 | 7:122642549 | GTTTCACCCAACAGC[-/TTT]TTTTTTTTTTTTTTA | 93664 |
rs199626946 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122645414 | ATGTACATATACACA[C/T]ATGTATATGTGTGTA | 93664 |
rs199627947 | in-del | -/AG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122645524 | ATACTTATATATATA[-/AG]TAAGTATATATATAT | 93664 |
rs199641488 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122726362 | GCTAATCACAGGCTT[G/T]CGTACGTTACTTGTT | 93664 |
rs199643111 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122820711 | ACTACAGGCGCCCGC[C/T]ACCACGCCCGGCTAA | 93664 |
rs199643380 | snp | C/G | 0.00229963 | 0.0338308 | missense | CADPS2 | GRCh38.p7 | 7:122393451 | CCTACTTGACAGGCT[C/G]CCATGTCTCCTGCTC | 93664 |
rs199648653 | in-del | -/TATTATC | 0.173965 | 0.238157 | intron-variant | CADPS2 | GRCh38.p7 | 7:122705505 | ATTATCTATATTATA[-/TATTATC]TATATTTATATTGTG | 93664 |
rs199652045 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122726004 | CCTAAACAGTTTGAA[-/T]TTTTTTTTTTCAAAT | 93664 |
rs199652391 | in-del | -/GAC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122451519 | TATTGATCGAACATT[-/GAC]TACTTTTATATATTT | 93664 |
rs199662352 | in-del | -/AC/ACAC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122645240 | GCTAAGTATATATAT[-/AC/ACAC]ACACACATGTACATG | 93664 |
rs199663080 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122746042 | TTCTTCATCTATATA[-/A]TAAGGCAGTAAAAAT | 93664 |
rs199674903 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122346550 | ATGAAATGTAAAATA[C/T]CTTGTGGATTATCCA | 93664 |
rs199682929 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122668245 | AATTGGAAAATTCCA[A/T]TTTTTTTTACTGGGG | 93664 |
rs199683423 | in-del | -/AT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122706181 | ATATTCAAGGAATAC[-/AT]ATATATGCTTATATA | 93664 |
rs199685799 | in-del | -/A/AA | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122603470 | AGCAGAAAAAAAAAA[-/A/AA]CACTCAAAGCAAAGG | 93664 |
rs199686494 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122722716 | AAAAAGAGCCTGCAT[C/T]GCCAAGACAATCCTA | 93664 |
rs199691234 | snp | A/G | | | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122704045 | TATTTTCTATCATGT[A/G]TAGGTTATCTTCTAT | 93664 |
rs199695203 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122484508 | AAATTAACTGAAAAT[G/T]GTTGTAAAATGTAAA | 93664 |
rs199698902 | snp | A/C | 0.00478085 | 0.0486577 | utr-variant-3-prime | CADPS2 | GRCh38.p7 | 7:122319950 | ATGCTCTTCTCCAAA[A/C]AAACAAACAAACAAA | 93664 |
rs199711943 | in-del | -/AA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122658919 | TATGTAAAAAAAAAA[-/AA]GTTTCTCGTACTTAT | 93664 |
rs199713510 | snp | A/G | 0.00133109 | 0.0257638 | missense | CADPS2 | GRCh38.p7 | 7:122474490 | GAAATAAACTCATCC[A/G]TACCATGTTTCTGAA | 93664 |
rs199716788 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122645525 | ATACTTATATATATA[A/T]AAGTATATATATATA | 93664 |
rs199716984 | in-del | -/ATATA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122428467 | CATATATATATATAT[-/ATATA]TTTTTTTTTTTTTGA | 93664 |
rs199720123 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122696514 | ATGACCCCATGGTCA[G/T]GGAAGCAGTTATAGC | 93664 |
rs199722643 | in-del | -/TTT | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122812449 | GAGAGCAAGCAAAGA[-/TTT]AAGAAAGAAAAAAAG | 93664 |
rs199730957 | snp | C/G | 2.23541e-05 | 0.00334314 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554724 | CACATTTAAACGCAT[C/G]ATACGGAGTGTCTAT | 93664 |
rs199732801 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122819867 | CATGCACCCCTTACC[A/G]TCTCATTAAAACCTA | 93664 |
rs199738288 | in-del | -/T | 0.0376037 | 0.131863 | intron-variant | CADPS2 | GRCh38.p7 | 7:122355038 | GTATGATTTTTTTTT[-/T]CATTCATAAAGTGTC | 93664 |
rs199745333 | in-del | -/C | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122715805 | CCTAGTAAGGTACTA[-/C]CCAAAGCTTAAAGTC | 93664 |
rs199748399 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122512750 | TATATGTATTATGCT[A/T]TATATATAAAATATA | 93664 |
rs199752073 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122463325 | CTTCATATTCTTAGA[A/T]TTTTTTTTTTTTGAG | 93664 |
rs199763839 | in-del | -/AA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122640934 | GCAAGACTCTATCTC[-/AA]AAAAAAAAAAAAAAA | 93664 |
rs199764715 | snp | C/T | 3.31246e-05 | 0.00406955 | intron-variant, synonymous-codon | CADPS2, RNF148 | GRCh38.p7 | 7:122702253 | GACTCCTTTCTGAAT[C/T]GAGTGCAAAATTTCC | 93664 |
rs199768783 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122405662 | AGCTCTGTCTCAAAC[-/A]AAAACAAACAAAAAA | 93664 |
rs199769696 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122457457 | ATTAATGGCTGTCAA[C/G]ATTTTCCAAAACACA | 93664 |
rs199770360 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122783109 | TGGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 93664 |
rs199773704 | in-del | -/T | 0.0123036 | 0.0774623 | intron-variant | CADPS2 | GRCh38.p7 | 7:122424975 | TAATTGTGTAATAGC[-/T]TTTTTTAAAAAAATT | 93664 |
rs199780654 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554188 | TCTATGGAAGTTTAA[A/G]TATTTCTAGGAACCT | 93664 |
rs199802800 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122601391 | AAGACTTCACATCTT[C/T]GCCAACCAGATCCAT | 93664 |
rs199806229 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122838162 | TCCAGCATATAAACA[G/T]AACCAAAGACAAAAA | 93664 |
rs199811577 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122427144 | TGTGTGTGTGTGTGT[G/T]TTAACTTTTTCTTTT | 93664 |
rs199812030 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122713315 | TTAAATCCTGTACTT[A/T]ACACTAGCTCTACAA | 93664 |
rs199812944 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122469823 | GAAGCAGGTGTGTGT[C/G]TGTGTGTGTGTGTGT | 93664 |
rs199818209 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122682592 | TATGTTTACTATCTG[-/A]AAAAAAATATGTGTT | 93664 |
rs199819452 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122458253 | ATTTCCCACCAATAT[-/C]CATTTGTGAACAGAA | 93664 |
rs199829329 | in-del | -/A | 0.0130921 | 0.0798413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122476436 | ATACAAACTTTAAAT[-/A]AAAAAATGTTTCTGA | 93664 |
rs199834650 | snp | C/T | 0.00299544 | 0.0385843 | synonymous-codon, utr-variant-5-prime | CADPS2 | GRCh38.p7 | 7:122621664 | TGAAGACCGCAACTC[C/T]TCTATATACATATTC | 93664 |
rs199845113 | in-del | -/AACAGACA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122722397 | TTCTTCTACACCAAT[-/AACAGACA]AACAGAGAGCCAAAT | 93664 |
rs199845810 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122668839 | GAGGAAGCCCTGTCT[C/T]CCCCACCACCACTTT | 93664 |
rs199846222 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122637206 | TTTTTTTTTTTTTTT[C/T]TTCCTGAGACAGGGT | 93664 |
rs199850827 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122678879 | AACCATGGCAGAACA[A/T]AAATTGTGAAGATTT | 93664 |
rs199864996 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122585400 | ACACAGTTAGAAAAA[C/T]CATAAATTCTAGAAT | 93664 |
rs199872471 | in-del | -/TG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122696518 | CCCATGGTCATGGAA[-/TG]GCAGTTATAGCTAAC | 93664 |
rs199897572 | snp | A/G | 0.000447231 | 0.0149471 | intron-variant, synonymous-codon | CADPS2, RNF148 | GRCh38.p7 | 7:122702400 | CTTCTCTGCTGCCAC[A/G]TTGATTTTATGTGTA | 93664 |
rs199900394 | in-del | -/CCC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122611467 | ATTGAAAAATTAATG[-/CCC]GCATTAACTTTTAAT | 93664 |
rs199905088 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122478682 | ATAGGTAATACAGAC[C/T]TGAAAATAGGTGGCA | 93664 |
rs199905513 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122876020 | TAACAGATATAACTT[-/A]AAAAAAAAAATGGAA | 93664 |
rs199913558 | snp | C/T | 0.000430784 | 0.0146699 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122629269 | CATTTTATCTGCCAA[C/T]TGCAGCCGGCCATCA | 93664 |
rs199923791 | snp | A/C | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122544222 | ACAGTATGTTTGTAG[A/C]AAGCCATATTGTGCA | 93664 |
rs199925802 | in-del | -/AA | 0.0240643 | 0.107019 | intron-variant | CADPS2 | GRCh38.p7 | 7:122837973 | TGGCAGAGACACAAC[-/AA]AAAAAAAGAGAATTT | 93664 |
rs199945859 | in-del | -/TTC | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122499436 | TGGTCTCTAAAGTTT[-/TTC]TTTTTTTTCCTTCAC | 93664 |
rs199949211 | in-del | -/AT | 0.0490535 | 0.14873 | intron-variant | CADPS2 | GRCh38.p7 | 7:122645345 | TATACACACATGTAC[-/AT]GTGTGTGTATACATG | 93664 |
rs199950021 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122839582 | TCAAACAAATTTACA[A/G]GAAAAAAACAAACAA | 93664 |
rs199951444 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122812423 | TGGAAAAAAAAAAAA[A/G]AGAGAGAGAGAGAGA | 93664 |
rs199956224 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122410460 | TTTTTTTTTTTTTTT[G/T]TAGTAAATATAGTTT | 93664 |
rs199957749 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122492016 | CTCTATTAAAAATAC[-/A]AAAAAATTAGCCAGG | 93664 |
rs199982377 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122817798 | ACCTCGTATCTCTGC[A/G]CCCCAATCCCTTATT | 93664 |
rs199995159 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122762035 | ATATATATATACACA[C/T]ACACACACACACACA | 93664 |
rs200019128 | in-del | -/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122833560 | GTTTGTTTTGTTTTG[-/T]TTTTTTTGTAATTTT | 93664 |
rs200025832 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122521814 | TTATATTAGGTATCA[-/C]ATTTTATAGAATTGT | 93664 |
rs200036624 | in-del | -/AT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122774242 | TCTCTTCAACAACAA[-/AT]ATATATATATAGACA | 93664 |
rs200038957 | in-del | -/AT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122645327 | TGTGTATACATGTAC[-/AT]ATATACACACATGTA | 93664 |
rs200043459 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122801778 | TTTTAATTTTTATTT[-/A]TTTTTTTTTTCTGGA | 93664 |
rs200060962 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122668253 | ATTCCATTTTTTTTT[-/T]ACTGGGGTGTCTAGA | 93664 |
rs200062547 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122607480 | TATAAAAGACTTTTC[C/T]GAAAAAACTGTCACA | 93664 |
rs200067009 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122798001 | GTTTTTTTGTGCAGG[-/T]TTTTTTTTTCAATGT | 93664 |
rs200069605 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122794767 | AAAAAAAAAAAAAAA[-/A]CCCTTTCTGACAACA | 93664 |
rs200074600 | snp | A/T | 2.65234e-05 | 0.00364157 | missense | CADPS2 | GRCh38.p7 | 7:122471542 | ATCTAACACAAAGAC[A/T]TGGCCAGGGCTAAAC | 93664 |
rs200075482 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122323839 | AACTGTTATGTATGT[A/G]TATATATATGCATAT | 93664 |
rs200075872 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122460965 | ATAATTTTGTTGGGA[A/C]AAGCCACACTAATTC | 93664 |
rs200087198 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122369125 | CTAGAAGAATTTTTG[-/T]TTCCCCCCCCCCCCC | 93664 |
rs200092083 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122423928 | AAGGTGACCTACGTA[A/G]ACTTTGATTATTTCC | 93664 |
rs200103936 | in-del | -/T | 0.0217236 | 0.101931 | intron-variant | CADPS2 | GRCh38.p7 | 7:122359695 | GCTCTACATATGTGA[-/T]TTTTTTTCTACTTAT | 93664 |
rs200107736 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122820113 | TGTGGTGCCAAACCC[A/G]TATACTCTCCTATCC | 93664 |
rs200113037 | snp | A/C/G | 0.000149779 | 0.00865273 | intron-variant, missense, stop-gained | CADPS2, RNF148 | GRCh38.p7 | 7:122702027 | CTTCTTTGAGAACTC[A/C/G]CAGTTGAAGCTGGTC | 93664 |
rs200119221 | in-del | -/T | 0.0349115 | 0.127424 | intron-variant | CADPS2 | GRCh38.p7 | 7:122514329 | TACAATTCTGAGTGA[-/T]TTTTTTAAAGGAGCA | 93664 |
rs200120580 | in-del | -/GGCTT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122337831 | GACAATATAGAAACA[-/GGCTT]GACTATGACTATCTT | 93664 |
rs200131174 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122584946 | TGAGTGCTCACAAAG[-/A]AAAAAAAAATTCTCC | 93664 |
rs200133219 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122720486 | TATGTATGTATGTAT[A/G]TATGTATATGTATAT | 93664 |
rs200136303 | in-del | -/A | 0.0103295 | 0.0711199 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122537940 | CTAATAATAATCTGG[-/A]AAAAAAATACTTTCC | 93664 |
rs200145673 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122878032 | GGGAGGCCGAGGCGG[G/T]GGATCATGAGGTCAA | 93664 |
rs200171193 | snp | C/T | 0.000231873 | 0.0107649 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122702356 | CTGCCCGTACCTTGA[C/T]AGTTGTAGATGATCA | 93664 |
rs200175110 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122404630 | GAAAGGTGTTCCTAT[C/T]TCTCCACATCCTCTC | 93664 |
rs200178541 | in-del | -/AT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122645338 | TACATATATACACAC[-/AT]ATGTACATGTGTGTG | 93664 |
rs200190743 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122625068 | ATTTTTTTTTTTTTT[A/G]AGACAGAGTTTCGCT | 93664 |
rs200191024 | in-del | -/TATATATATATATATATATA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122323874 | TACATATGTATATTT[-/TATATATATATATATATATA]TATATATATATATAT | 93664 |
rs200195320 | snp | C/G | 0.00146115 | 0.0269896 | missense, utr-variant-5-prime | CADPS2 | GRCh38.p7 | 7:122663544 | CTCTGTACCATTCTG[C/G]CCACTCGGTCACTCT | 93664 |
rs200200154 | snp | A/T | 2.43786e-05 | 0.00349124 | intron-variant | CADPS2 | GRCh38.p7 | 7:122474539 | ATTCAGGAAAGCATG[A/T]ACAGTATATTTACTT | 93664 |
rs200210311 | in-del | -/TTATG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122876757 | AAAATAAGTGAAAAA[-/TTATG]TTATATCTGAAAATA | 93664 |
rs200230327 | in-del | -/TATG | 0.172028 | 0.23753 | intron-variant | CADPS2 | GRCh38.p7 | 7:122720471 | ATGTATATGTAGATA[-/TATG]TATGTATGTATATAT | 93664 |
rs200231189 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122655655 | TTCACTTTGTGGCAG[G/T]GGTCTGGAACTGGAC | 93664 |
rs200231597 | in-del | -/ATT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122760312 | ATGTATATTTAGGTA[-/ATT]ATTTATAGATATAGT | 93664 |
rs200233722 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122645246 | GTATATATATACACA[C/T]ATGTACATGTGTGTA | 93664 |
rs200238478 | snp | A/C/T | 0.00478364 | 0.0487146 | intron-variant | CADPS2 | GRCh38.p7 | 7:122871153 | GAAGACAGGGGACAA[A/C/T]GGAGGAGGGGAGAGA | 93664 |
rs200253044 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122368505 | CCTCATCTGTGAACA[A/G]GGAGACTGGACTGGT | 93664 |
rs200261046 | in-del | -/CACACG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122328156 | ACACACACACACACA[-/CACACG]CACGCACACACCTTA | 93664 |
rs200261179 | in-del | -/A | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122707369 | CTATTATTAAGAGAG[-/A]AAAAAATCAACTAAC | 93664 |
rs200261263 | snp | C/T | 3.69754e-05 | 0.00429957 | missense, intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554684 | AGAAGTTGGGTATAA[C/T]ATCACCTGTATGGAA | 93664 |
rs200268245 | in-del | -/CTTTCTGTTTCTCTCCATCTCTCTTT | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539775 | TGTCTCTGTCTCTCT[-/CTTTCTGTTTCTCTCCATCTCTCTTT]GTCCATCTCTGTCTT | 93664 |
rs200268756 | snp | C/G | 0.000510974 | 0.0159758 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698228 | GTCCAAATGTGTTCT[C/G]AAGATCTGTTGTTAA | 93664 |
rs200270434 | in-del | -/AAATAAAT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122878640 | GCAAGACTCTGTCTC[-/AAATAAAT]AAATAAATAAATAAA | 93664 |
rs200287126 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122519679 | ATTCATCTATGACTT[-/A]AAAAAAAAATCCAGC | 93664 |
rs200310765 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539747 | TGTCTGTCCCTCTCT[C/G]TCTGTCTCTCTCTGT | 93664 |
rs200310936 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122416297 | ATACATTATTTAGAC[-/A]AAAAAAAAAAAACAG | 93664 |
rs200322814 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122591137 | AGCAACTTCAGCAAA[C/G]TCTCAGGATACAAAA | 93664 |
rs200334358 | snp | A/G | 0.000102999 | 0.00717558 | synonymous-codon, utr-variant-5-prime | CADPS2 | GRCh38.p7 | 7:122737063 | CTGCAACTGTTGTTT[A/G]TTAAGCTACAAGAAA | 93664 |
rs200334796 | in-del | -/AT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122706812 | TATACACACACACAC[-/AT]ATATATATATGTATG | 93664 |
rs200334965 | in-del | -/TTTTC | 0.0174175 | 0.0916809 | intron-variant | CADPS2 | GRCh38.p7 | 7:122575417 | GAAATGTTCAATTCT[-/TTTTC]TTTTCTTTTCTCTTC | 93664 |
rs200337204 | snp | G/T | | | stop-gained | CADPS2 | GRCh38.p7 | 7:122416100 | CTGTAAGACTTCTAT[G/T]CAGAGCTCTGCCAGA | 93664 |
rs200358605 | in-del | -/A | 0.0912534 | 0.193131 | intron-variant | CADPS2 | GRCh38.p7 | 7:122584176 | CTGAAAGAGTTTGTC[-/A]AAAAAATGATAATTA | 93664 |
rs200360514 | snp | A/T | 0.000215602 | 0.0103805 | missense | CADPS2 | GRCh38.p7 | 7:122388696 | AAACATTTGCAGTGC[A/T]TCAAGCTTCCAAAAA | 93664 |
rs200371879 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122818515 | TCCCGCCTGTCCCCT[C/T]AGTACCAACCCCAAG | 93664 |
rs200372150 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122618043 | TGCAAGATTCCATCT[A/C]AAAAAAAAAAAAAAT | 93664 |
rs200378689 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122744982 | TTTCTTTTTTTTTTT[A/T]CTTTATTGAACTATA | 93664 |
rs200386702 | snp | A/G | 0.000675561 | 0.0183664 | intron-variant | CADPS2 | GRCh38.p7 | 7:122615171 | AATACACTTTTTTCA[A/G]CTGGCTTACTGTGGC | 93664 |
rs200386723 | in-del | -/ACTTAG | 0.312593 | 0.242037 | intron-variant | CADPS2 | GRCh38.p7 | 7:122819619 | CCAACTCTGGTGCCA[-/ACTTAG]ACAGTACTCTTTTAA | 93664 |
rs200391817 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122448929 | TAAAGAAAAAAAAAA[-/A]TAAAAAAATTATGTT | 93664 |
rs200400661 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122757092 | GAAGCTCTGAACTGT[G/T]GACCAAAGGGCAATG | 93664 |
rs200430516 | in-del | -/T | 0.0372196 | 0.131242 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539895 | AAACATTTTTTCACC[-/T]TTTTTTTTCCATTTT | 93664 |
rs200431591 | in-del | -/G | 0.0119091 | 0.0762411 | intron-variant | CADPS2 | GRCh38.p7 | 7:122384462 | TTGCTTTTTATAAAT[-/G]AGGTCCGCTGGCTCA | 93664 |
rs200432571 | snp | A/G | 0.347694 | 0.230122 | intron-variant | CADPS2 | GRCh38.p7 | 7:122801067 | CACTATTTGGGCTAA[A/G]GAGAAAATTAAAATG | 93664 |
rs200436034 | snp | C/T | 0.332799 | 0.23589 | intron-variant | CADPS2 | GRCh38.p7 | 7:122569563 | AACCAAAAAAGAGCC[C/T]GCATTGCCAAGACAA | 93664 |
rs200436780 | snp | A/G | 0.000231888 | 0.0107652 | missense | CADPS2 | GRCh38.p7 | 7:122393520 | TGAGATCCACATAGC[A/G]GACAACCAAGGGTAC | 93664 |
rs200447537 | in-del | -/A | 0.0376037 | 0.131863 | intron-variant | CADPS2 | GRCh38.p7 | 7:122515939 | TAAAAATATATTTGG[-/A]AAAAAAACATGCAAA | 93664 |
rs200463069 | in-del | -/TTTATATATTCATATG | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122541806 | ATATATTCATATATA[-/TTTATATATTCATATG]TTTATATATTCATAT | 93664 |
rs200478414 | in-del | -/TT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122493721 | TGGTTATGTTTAATC[-/TT]TTTTTTTTTTTTTTT | 93664 |
rs200484938 | in-del | -/AC | 0.0490535 | 0.14873 | intron-variant | CADPS2 | GRCh38.p7 | 7:122405138 | ACAAAAAACAAAAAA[-/AC]AAAACAAAACAAAAA | 93664 |
rs200486960 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122361103 | ATCAATTTCTTCCAT[C/T]GCACAAAAATTCACA | 93664 |
rs200488419 | in-del | -/TAT | 0.0726307 | 0.176182 | intron-variant | CADPS2 | GRCh38.p7 | 7:122650900 | TAACACATATATAAA[-/TAT]TATGGCCACTCCAAT | 93664 |
rs200489350 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122527749 | TAAGAGGACAGGCTG[A/C]TCCATGAGAAGATCT | 93664 |
rs200493226 | in-del | -/TTG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122486922 | TGAAGTCTCAGGTGA[-/TTG]TTATTTTTAGCAATA | 93664 |
rs200494389 | in-del | -/TTTT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122642549 | GTTTCACCCAACAGC[-/TTTT]TTTTTTTTTTTTTAC | 93664 |
rs200498336 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539762 | CTCTGTCTCTCTCTG[C/T]CTCTGTCTCTCTCTT | 93664 |
rs200507016 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122594358 | TTGGGAAATGGGTTG[A/C]GGTGGGTAATGACTT | 93664 |
rs200522504 | snp | C/T | 0.000522284 | 0.0161514 | synonymous-codon, utr-variant-5-prime | CADPS2 | GRCh38.p7 | 7:122663561 | CACTCGGTCACTCTT[C/T]AGAAAAACCTGAAAA | 93664 |
rs200528100 | snp | A/G | | | stop-gained | CADPS2 | GRCh38.p7 | 7:122345618 | CATTGACCTTTTCTC[A/G]AAGAATATCTTGGTT | 93664 |
rs200528356 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122679730 | CTTTAAAATTTCTCT[C/T]TTTTGTACTCTTTCC | 93664 |
rs200534497 | snp | A/C | | | utr-variant-3-prime | CADPS2 | GRCh38.p7 | 7:122319954 | TCTTCTCCAAAAAAA[A/C]AAACAAACAAACAAA | 93664 |
rs200555155 | snp | A/C/G | 0.00335897 | 0.0408441 | intron-variant | CADPS2 | GRCh38.p7 | 7:122393419 | AGGCAGGTGCTCTAC[A/C/G]GACACTAGGTAAGAT | 93664 |
rs200568308 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122611326 | TGGGCTAAGAAAAAA[A/G]AAAGGCTATTCAAAT | 93664 |
rs200570930 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122770639 | AATTAGTGCCCAGTA[A/C]AGCTTGCTTGGAGCA | 93664 |
rs200575940 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122660620 | TTAAAAAAAAAAAAA[A/G]AAAACTTGGGCCAAG | 93664 |
rs200576958 | in-del | -/T | 0.0189856 | 0.0955633 | intron-variant | CADPS2 | GRCh38.p7 | 7:122477175 | CTGGCCCTCTGGCCC[-/T]TGTTTTAAACAAAAT | 93664 |
rs200590801 | snp | A/G | 0.000403592 | 0.0141998 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122471536 | GTACTCATCTAACAC[A/G]AAGACTTGGCCAGGG | 93664 |
rs200593889 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122323835 | GTACAACTGTTATGT[A/G]TGTGTATATATATGC | 93664 |
rs200620103 | in-del | -/AG | 0.266689 | 0.249442 | intron-variant | CADPS2 | GRCh38.p7 | 7:122640491 | CACACACACACACAC[-/AG]AGATAGAGAGAGAGA | 93664 |
rs200625068 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122355602 | AAAAAAAAAAAATTC[C/T]GACAAGTGACGGTAT | 93664 |
rs200626659 | snp | C/T | 0.0039921 | 0.0444985 | missense, utr-variant-5-prime | CADPS2 | GRCh38.p7 | 7:122736977 | TAACTCCGAACTGCG[C/T]TGCAAAATGCTTCGT | 93664 |
rs200629961 | in-del | -/GGA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122580013 | AAAAATTTCTAGTAT[-/GGA]ACAGAATGATCCTAG | 93664 |
rs200631630 | snp | A/T | 0.0039921 | 0.0444985 | intron-variant | CADPS2 | GRCh38.p7 | 7:122345534 | TTCTCTTTGCAGTTT[A/T]TCTATGGTGTCAGCA | 93664 |
rs200636100 | snp | A/G | 1.64882e-05 | 0.00287121 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698338 | GTTGTGACAATCACA[A/G]AAGAGACCAAATAGT | 93664 |
rs200637139 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122428467 | CATATATATATATAT[A/T]TATATTTTTTTTTTT | 93664 |
rs200645297 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122428473 | TATATATATATATAT[A/T]TTTTTTTTTTTGAGA | 93664 |
rs200651726 | snp | C/T | 0.000357577 | 0.0133664 | missense | CADPS2 | GRCh38.p7 | 7:122451392 | AAATGGCTTATCTGA[C/T]TTTCTAAAAGGGAAG | 93664 |
rs200654344 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122846812 | TCTTCAAGCTGGCAC[A/C]ACTCCCTTATAGAAG | 93664 |
rs200660901 | in-del | -/A | 0.00557542 | 0.0525036 | intron-variant | CADPS2 | GRCh38.p7 | 7:122730378 | TGAGGGCAATTTAAT[-/A]AATCTGTATAAATAA | 93664 |
rs200661784 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122797013 | TACAAGAAAAAAAAA[-/A]CATTAAAAAGCAGGC | 93664 |
rs200667006 | snp | A/G | 1.65723e-05 | 0.00287852 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122702152 | AAGTAGGCAATTGTG[A/G]CAGCCAGGAAGGTAA | 93664 |
rs200673307 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122696517 | ACCCCATGGTCATGG[A/T]AGCAGTTATAGCTAA | 93664 |
rs200679861 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122484898 | CACGTGCTCATATCA[A/T]GACGTGCTCATATCA | 93664 |
rs200688578 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122437705 | ATGTGTTGAATAAAA[C/T]TGTTGAATAAAAGCT | 93664 |
rs200695685 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122875210 | AGTGTAGGTGTATAC[A/G]TATTATGGATACTTT | 93664 |
rs200698139 | in-del | -/TTAA | 0.0123036 | 0.0774623 | intron-variant | CADPS2 | GRCh38.p7 | 7:122879956 | CTTAAACAAGTCATT[-/TTAA]TTAATAAACAAGTCA | 93664 |
rs200730793 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122774265 | ATATAGACATAGATA[G/T]ATATACACACACACA | 93664 |
rs200739500 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122820893 | AGCCCTCATGTCTGC[A/G]TGCAGTGGCTGCCAC | 93664 |
rs200747929 | in-del | -/C | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122856447 | TCTCTTCTTGTTCAT[-/C]TTTACCTTCACCACC | 93664 |
rs200765883 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122637054 | TTAAATTGTTTATTT[-/A]TTTTTTTCTTTTTGT | 93664 |
rs200777400 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122511284 | TACAATTCCTTCATT[A/G]CCAAACTCTCTTATG | 93664 |
rs200782140 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122469825 | AGCAGGTGTGTGTCT[C/G]TGTGTGTGTGTGTGT | 93664 |
rs200787161 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122787677 | GGAGGCTACAATGTG[C/T]TTTGCATTGCACTAG | 93664 |
rs200787426 | snp | A/C | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122558082 | TCTTACAAACCTGAT[A/C]TTATTTTGAATTATT | 93664 |
rs200787557 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122364726 | AGTGAGACTCCATCT[A/C]AAAAAAAAAAAAAGA | 93664 |
rs200787901 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122828250 | ACCATTTCTACTATT[-/C]TTTTATCATTTACAT | 93664 |
rs200789691 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122527429 | GCTAAAAAAAAAAAA[A/C]ACACAAAACTGTCTG | 93664 |
rs200799885 | in-del | -/T | 0.0722614 | 0.17581 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554868 | TACAGACTCAATTTA[-/T]TTTTTTGACAAATAT | 93664 |
rs200811716 | in-del | -/ATCT | | | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122700577 | TACAACAATACCTAA[-/ATCT]TTCTGTCTCTCATTG | 93664 |
rs200819852 | snp | A/G | 0.312593 | 0.242037 | intron-variant | CADPS2 | GRCh38.p7 | 7:122820398 | CTCCCTGCCAATTGC[A/G]TCCGACTGATCTCTC | 93664 |
rs200832096 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122664099 | AAGATGATTAGGAAA[C/T]CAACTGGAGATATGA | 93664 |
rs200836860 | in-del | -/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122558201 | AATAATGAAGAATTG[-/T]TTTTTTTTTATTAGA | 93664 |
rs200839111 | in-del | -/TTT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122521816 | ATATTAGGTATCACA[-/TTT]TATAGAATTGTCCCT | 93664 |
rs200845599 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122484509 | AATTAACTGAAAATG[G/T]TTGTAAAATGTAAAC | 93664 |
rs200849620 | in-del | -/GTTA | 0.0244538 | 0.107838 | intron-variant | CADPS2 | GRCh38.p7 | 7:122713228 | ACAGTCTTAAGTCTC[-/GTTA]GTTTTACCAGGAATA | 93664 |
rs200855821 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122821044 | CTGGCTCCTTCAGCT[A/G]TACTCACTCTTTGTT | 93664 |
rs200856747 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122805160 | ATTTTCAATCATTAT[C/T]ATTATTATTATTGTT | 93664 |
rs200860090 | snp | C/T | 0.000162744 | 0.00901918 | intron-variant | CADPS2 | GRCh38.p7 | 7:122438508 | GGGCAGGGTTGGGGA[C/T]AGACAGATGGAAGAA | 93664 |
rs200861055 | snp | C/T | 1.6571e-05 | 0.0028784 | missense, utr-variant-5-prime | CADPS2 | GRCh38.p7 | 7:122621531 | ACAGCTGAATCTCAT[C/T]CTCATCTCCTATGTC | 93664 |
rs200865337 | snp | C/T | 8.28164e-05 | 0.00643439 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122702297 | TGCTTATCATCACCG[C/T]GACTATATTTTCCGT | 93664 |
rs200870044 | in-del | -/AT | 0.354019 | 0.227333 | intron-variant | CADPS2 | GRCh38.p7 | 7:122706313 | TTATATATTCAAGGA[-/AT]ATATATATATATGCT | 93664 |
rs200875460 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122729698 | TTTTTTTTTTTTTTT[A/T]CTGTTGAGTCCTTTG | 93664 |
rs200885946 | snp | A/C | 0.000399281 | 0.0141238 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122474456 | AAGGAAGGCATGATC[A/C]AGCTTGCAGGGGTTT | 93664 |
rs200914703 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122688769 | CATGGTTGTGGTAAC[A/G]GGGAGTTATACACCT | 93664 |
rs200914736 | in-del | -/ATA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122428469 | TATATATATATATAT[-/ATA]TTTTTTTTTTTTTGA | 93664 |
rs200925452 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122618259 | AACGGCTGTTTTTTT[G/T]ATACCATAAAAATCC | 93664 |
rs200926726 | in-del | -/ACACACACACACAC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122366611 | CTCCATCTCAAAAAT[-/ACACACACACACAC]ACACACACACACACA | 93664 |
rs200940863 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122518699 | ATTAACTCAAAGAAG[-/T]TTTTTTTTTAAGGGT | 93664 |
rs200952388 | in-del | -/ACGTGCTCATATCATG | 0.0603597 | 0.1629 | intron-variant | CADPS2 | GRCh38.p7 | 7:122484884 | CACTTTTTTAACAAC[-/ACGTGCTCATATCATG]ACGTGCTCATATCAT | 93664 |
rs200955483 | in-del | -/AT | 0.358515 | 0.225221 | intron-variant | CADPS2 | GRCh38.p7 | 7:122645414 | TACATATACACACAT[-/AT]GTATATGTGTGTATA | 93664 |
rs200971990 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122560990 | TGTCTAAGGGAAATC[C/T]ATATTATTCCTTAGT | 93664 |
rs200981819 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122380478 | CTATTTTTTTTTTTT[-/T]GTGCTGAAAACATGT | 93664 |
rs200984050 | snp | C/T | 0.000676613 | 0.0183807 | missense | CADPS2 | GRCh38.p7 | 7:122360992 | ACAGCTTAGACAACA[C/T]GCCTTCCAACACTGA | 93664 |
rs200986900 | in-del | -/A | 0.419776 | 0.18351 | intron-variant | CADPS2 | GRCh38.p7 | 7:122710050 | AACTTAAAGTATAAT[-/A]AAAAAAAAAAAAAAA | 93664 |
rs200988359 | snp | A/G | 0.000461513 | 0.0151837 | intron-variant, synonymous-codon | CADPS2, RNF133 | GRCh38.p7 | 7:122698307 | GTGATAAAAGATGAA[A/G]TATGCTAAGGTAGCA | 93664 |
rs201009223 | in-del | -/AAAT | 0.0111196 | 0.0737302 | intron-variant | CADPS2 | GRCh38.p7 | 7:122338420 | AACAAACAAACAAAC[-/AAAT]AAATAAATAAGTAAC | 93664 |
rs201010556 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122330546 | CTATCATACCTGGGT[A/T]CCATAAAACCAGACC | 93664 |
rs201018789 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122798106 | TGCAGTTGTTGCATT[-/A]AAAAAAAAACTCTAT | 93664 |
rs201028629 | in-del | -/ATA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122645496 | ATTTAGCGTATATAT[-/ATA]TAAGTATATATATAC | 93664 |
rs201034244 | in-del | -/TG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122583580 | ATATATCAGAATATA[-/TG]TGTGTGTGTATATAT | 93664 |
rs201036877 | in-del | -/AT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122652252 | TCTCTCTCTCTCTAC[-/AT]ATATATATATATGCT | 93664 |
rs201047624 | in-del | -/AAAT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122593019 | AATAAATAAATAAAT[-/AAAT]GTATTTGAAATTCCA | 93664 |
rs201065976 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122451713 | AGATTATAATAAATA[A/T]TTTCCAGATCTACCG | 93664 |
rs201068162 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122538675 | TGGGTAAGGAGATAG[A/G]AAAGTACACTGTAAG | 93664 |
rs201089082 | in-del | -/CAATT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122612429 | ATAAAATTAAGAAAA[-/CAATT]CAACTCAAAATAGCA | 93664 |
rs201098995 | snp | A/G | 0.000149282 | 0.00863822 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122701937 | TGCAAGTTAAAATGC[A/G]TACTACATCTTGGGG | 93664 |
rs201104778 | snp | A/T | 5.0213e-05 | 0.00501039 | missense | CADPS2 | GRCh38.p7 | 7:122345579 | AGCTACTTACATCAA[A/T]TAACTTTTCTATATA | 93664 |
rs201108842 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122776350 | GATTGTGAGGGCTCC[A/C]CAGCCATGAGGAACT | 93664 |
rs201109477 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122877560 | TGACCAGTTAATTAC[-/A]AAAAAAAAGCTTCCC | 93664 |
rs201111180 | in-del | -/AAGA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122437802 | AATGAATAAAGCCTG[-/AAGA]AAGAAAAAAAAAAAA | 93664 |
rs201121469 | in-del | -/A | 0.0125725 | 0.0782826 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122540004 | TTTTATATTTAATAT[-/A]TTTACTCTTTTGTGT | 93664 |
rs201126719 | in-del | -/TATATATATATATATATATATATATATA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122323874 | TACATATGTATATTT[-/TATATATATATATATATATATATATATA]TATATATATATATAT | 93664 |
rs201127108 | in-del | -/TTAT | 0.0345262 | 0.126772 | intron-variant | CADPS2 | GRCh38.p7 | 7:122514351 | AAAGGAGCATTATGA[-/TTAT]TTATTTAGGGGCTTA | 93664 |
rs201141220 | snp | C/G | 0.00012055 | 0.00776277 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122702720 | ATGAAACAGAACTAT[C/G]CGTCGAAGGGGTAAT | 93664 |
rs201160437 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122757689 | TCAATCCCTAGCTGA[G/T]TTTTTTAAAACAACT | 93664 |
rs201165990 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122405139 | CAAAAAACAAAAAAA[-/C]AAAACAAAACAAAAA | 93664 |
rs201169308 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122869864 | AGAGTTTGTGCAAGC[A/G]ATCAAAGTTATTATC | 93664 |
rs201171221 | in-del | -/ATAG | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122774258 | TATATATATATAGAC[-/ATAG]ATAGATATACACACA | 93664 |
rs201174338 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122761682 | ACGTATTAAGCAAAC[-/A]AAAAAAAAGCTCTTG | 93664 |
rs201174725 | snp | A/G | 5.35547e-05 | 0.00517441 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122388681 | GTGCAGATCAAAGAC[A/G]AACATTTGCAGTGCA | 93664 |
rs201194842 | snp | A/G | 0.0718919 | 0.175435 | intron-variant | CADPS2 | GRCh38.p7 | 7:122570680 | AAATGTGGCACATAT[A/G]CACCATAGAATACTA | 93664 |
rs201196398 | in-del | -/GTGGTGGTGGTG | 0.499587 | 0.0143711 | intron-variant | CADPS2 | GRCh38.p7 | 7:122528111 | TAGATGAAGGCATTA[-/GTGGTGGTGGTG]GTGGTGGTGGTGGTG | 93664 |
rs201199241 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122501745 | CCAGGCGTGGTGGCA[A/C]ACGCCTGTAGTCCCA | 93664 |
rs201202910 | in-del | -/CA | 0.0329836 | 0.124112 | intron-variant | CADPS2 | GRCh38.p7 | 7:122820500 | CACAAGAGCCAGGAC[-/CA]CACACCCTGTAGCCT | 93664 |
rs201203152 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122637208 | TTTTTTTTTTTTTTT[C/T]CCTGAGACAGGGTCT | 93664 |
rs201207816 | in-del | -/AAC | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122328080 | CACTAAGAATAGCCT[-/AAC]AACAACAAAAATCCC | 93664 |
rs201210175 | in-del | -/TT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122759981 | GTGTATATAGGTGTA[-/TT]TTTTATATATATATA | 93664 |
rs201215032 | snp | A/G | 4.98409e-05 | 0.00499179 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122702590 | CTCTCTCCTAATTCC[A/G]ATGTGATCTCATTTC | 93664 |
rs201224741 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122363644 | CTTCTCAGTAAAGTG[A/G]GGAAAAGGACAGCTA | 93664 |
rs201225252 | in-del | -/T | 0.0130921 | 0.0798413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122379275 | ATCTTTTAAACTACA[-/T]TTTTTTCTCAATTAG | 93664 |
rs201237790 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122481282 | GTCAGCAGAGGTCTG[G/T]CCTGATTTAAAACTT | 93664 |
rs201248348 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122637054 | TTAAATTGTTTATTT[A/T]TTTTTTTCTTTTTGT | 93664 |
rs201249579 | snp | A/T | 0.00264158 | 0.0362466 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554521 | GAAATTCAATAATTC[A/T]GGAAAAAAATCCTCA | 93664 |
rs201252710 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122879057 | CCTGGCCAACATGGA[A/G]AAACCCCATCTCTAC | 93664 |
rs201255578 | snp | A/G | 0.000131807 | 0.00811701 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698600 | AGGTACAACCTCCCC[A/G]TTCAATAAGTGCAAG | 93664 |
rs201256882 | in-del | -/A | 0.0166325 | 0.0896639 | intron-variant | CADPS2 | GRCh38.p7 | 7:122515951 | GGAAAAAAAACATGC[-/A]AAAAAAAGAATAATA | 93664 |
rs201266932 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122645296 | ACATATGTACATATA[C/T]ACACATATGTACATG | 93664 |
rs201268475 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122775022 | TCTCAACTATGTGTG[-/T]TTTTTTTTAAAATAC | 93664 |
rs201271355 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122742211 | GCGTGGCCAACGTGG[A/T]GAAACCCCGTCTCTA | 93664 |
rs201275319 | in-del | -/AAAAG | 0.0360663 | 0.129354 | intron-variant | CADPS2 | GRCh38.p7 | 7:122879557 | AAAAATAAAAATAAA[-/AAAAG]AAAAGAAAAGAAAAG | 93664 |
rs201284471 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122838161 | ATCCAGCATATAAAC[A/C]GAACCAAAGACAAAA | 93664 |
rs201294686 | snp | C/T | 0.000149337 | 0.00863979 | missense | CADPS2 | GRCh38.p7 | 7:122393555 | ATTTCTTGCAAGTGT[C/T]TGTGAAATTTTCCAT | 93664 |
rs201294958 | in-del | -/AT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122371994 | ATTAGAGGAACAATA[-/AT]AACAATATCAACTAA | 93664 |
rs201297535 | in-del | -/A | 0.0236746 | 0.106192 | intron-variant | CADPS2, RNF148 | GRCh38.p7 | 7:122701621 | AAATAAAATTCACCT[-/A]AAAAAAACAATTAAA | 93664 |
rs201297740 | in-del | -/TTTT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122427143 | GTGTGTGTGTGTGTG[-/TTTT]AACTTTTTCTTTTTT | 93664 |
rs201299372 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539753 | TCCCTCTCTCTCTGT[C/T]TCTCTCTGTCTCTGT | 93664 |
rs201301272 | in-del | -/TA | 0.0607341 | 0.163335 | intron-variant | CADPS2 | GRCh38.p7 | 7:122645231 | TATATATACGCTAAG[-/TA]TATATATATACACAC | 93664 |
rs201305195 | in-del | -/ATT | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122635284 | TAATTTTTTTTTTTA[-/ATT]ATTATTATTATACTT | 93664 |
rs201311280 | in-del | -/C | 0.0189856 | 0.0955633 | intron-variant | CADPS2 | GRCh38.p7 | 7:122428072 | GTTAATATTTTTTAG[-/C]TAGTGGATTGATGGA | 93664 |
rs201316078 | in-del | -/AAAAC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122405135 | AAAACAAAAAACAAA[-/AAAAC]AAAACAAAACAAAAA | 93664 |
rs201341069 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122484510 | ATTAACTGAAAATGG[G/T]TGTAAAATGTAAACG | 93664 |
rs201355361 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122323895 | TATATATATATATAT[A/T]TATATATATATATAT | 93664 |
rs201364559 | in-del | -/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122552776 | TATGATAGGTTCCTG[-/T]TTTTTTTTTTTTTTT | 93664 |
rs201366088 | snp | A/C | 0.0029954 | 0.038584 | intron-variant | CADPS2 | GRCh38.p7 | 7:122621434 | CAGAAATTATTGTGC[A/C]TCATCATTTATGCTG | 93664 |
rs201370115 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122659327 | AAAAAAAAAAAAAAA[A/C]ACCGTGGAAAAAAAT | 93664 |
rs201371629 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122713316 | TAAATCCTGTACTTA[A/C]CACTAGCTCTACAAC | 93664 |
rs201371757 | in-del | -/T | 0.0271762 | 0.113356 | intron-variant | CADPS2 | GRCh38.p7 | 7:122813129 | GTACGGAAAAAAAAG[-/T]TTTTAAAAAGTTGGT | 93664 |
rs201372995 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122497177 | GCATCTGGTAAATTT[-/A]AAAAAAAAATCTCTT | 93664 |
rs201376204 | in-del | -/GAT | 0.00504972 | 0.0499936 | intron-variant | CADPS2 | GRCh38.p7 | 7:122386339 | GGGTGGAAAAAAAAA[-/GAT]GATGAAAGAGAACAG | 93664 |
rs201395313 | snp | A/G | 6.62493e-05 | 0.00575502 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122702296 | TTGCTTATCATCACC[A/G]CGACTATATTTTCCG | 93664 |
rs201401442 | snp | C/G | 0.184838 | 0.241358 | intron-variant | CADPS2 | GRCh38.p7 | 7:122722134 | TGAAAACTGGCACAA[C/G]ACAGGGATGCCCTCT | 93664 |
rs201415473 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122322899 | GGACAAGACTACTAA[-/C]AGCAAGTAGTTTGGG | 93664 |
rs201437168 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122822030 | CTATTCACCGTTCTC[A/G]ACTACTCATACACGC | 93664 |
rs201449744 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122660682 | TTGGGAGGCCGAGGC[A/G]GGCGGATCATGAGGT | 93664 |
rs201459075 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122870641 | TAACAACCTCACCAC[-/A]AAAAAGAAGATAAGT | 93664 |
rs201473530 | snp | C/T | 0.000140692 | 0.00838609 | intron-variant | CADPS2 | GRCh38.p7 | 7:122663232 | AAATATCAGAGACCA[C/T]TTACCTGACATGCAT | 93664 |
rs201474886 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122484505 | TAAAAATTAACTGAA[A/C]ATGGTTGTAAAATGT | 93664 |
rs201477505 | snp | A/G | 3.31873e-05 | 0.0040734 | missense | CADPS2 | GRCh38.p7 | 7:122581229 | CAGTGCTTTCTGTGA[A/G]GAGTTTCACTTTGAC | 93664 |
rs201480389 | snp | C/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539765 | TGTCTCTCTCTGTCT[C/G]TGTCTCTCTCTTTCT | 93664 |
rs201484787 | snp | C/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122549427 | AGTTACCATCGCACT[C/G]AAGACATTCGTGTGA | 93664 |
rs201484977 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122611327 | GGGCTAAGAAAAAAG[A/G]AAGGCTATTCAAATT | 93664 |
rs201498806 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | CADPS2 | GRCh38.p7 | 7:122837161 | ATGGAAACTGAACAA[A/C]CTGCTCCTGAATGAC | 93664 |
rs201508512 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122619930 | GAAGAAAGACTCATA[G/T]TTCTAATCTGACACT | 93664 |
rs201527881 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122408873 | GGCCTTAAAATAATA[G/T]ATATAAAATAATAAT | 93664 |
rs201529378 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122484899 | ACGTGCTCATATCAT[C/G]ACGTGCTCATATCAT | 93664 |
rs201536376 | snp | A/C | 0.0010627 | 0.0230265 | missense | CADPS2 | GRCh38.p7 | 7:122474446 | GTATTCTAAAAAGGA[A/C]GGCATGATCAAGCTT | 93664 |
rs201537224 | in-del | -/GCTCTGGATA | 0.039522 | 0.134904 | intron-variant | CADPS2 | GRCh38.p7 | 7:122424879 | CTGTCTACTTACTTT[-/GCTCTGGATA]GCTCTGGATAGCTCT | 93664 |
rs201538143 | snp | A/G | 0.000150705 | 0.00867926 | intron-variant, utr-variant-5-prime | CADPS2, RNF133 | GRCh38.p7 | 7:122698932 | ATCTCTCTCTTCTCC[A/G]AGTGACTTAAGAACC | 93664 |
rs201538526 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122670190 | GCATATATATATATA[-/T]AACACTGATCATTTA | 93664 |
rs201540773 | snp | A/C/T | 0.000199659 | 0.00998958 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122702026 | CCTTCTTTGAGAACT[A/C/T]GCAGTTGAAGCTGGT | 93664 |
rs201543398 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122762033 | ATATATATATATACA[C/T]ACACACACACACACA | 93664 |
rs201546521 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122565232 | TGAATTTATAGAATT[A/T]AAAAAAAAAAAACTT | 93664 |
rs201549696 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122393065 | GCTTAAAAACTCAAA[A/T]AAAAAAAAAAAAACA | 93664 |
rs201553729 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122668413 | GGTTAAAAAAAAAAA[-/C]AAAAACAAAAACAAA | 93664 |
rs201564513 | in-del | -/CATATATATTTATATATATG | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122541848 | ATATGTTTATATATT[-/CATATATATTTATATATATG]CATATATATTTATAT | 93664 |
rs201571666 | in-del | -/GT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122521808 | CTTCACTTATATTAG[-/GT]ATCACATTTTATAGA | 93664 |
rs201580999 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122323837 | ACAACTGTTATGTAT[A/G]TGTATATATATGCAT | 93664 |
rs201584595 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122506744 | AAAAAAAAAAAAAAA[G/T]AAACAAACTACACCA | 93664 |
rs201588839 | in-del | -/C | 0.0372196 | 0.131242 | intron-variant | CADPS2 | GRCh38.p7 | 7:122852105 | TGAAAAAGTTTTTTT[-/C]TATTAAAAATGAAGT | 93664 |
rs201591469 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122847609 | TAGATTTTTTTTTTT[C/T]TTGTCATCATTAACA | 93664 |
rs201594009 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122545356 | TACTAGAGTGGCAGG[A/G]TTTGGTAAAAGAGTG | 93664 |
rs201595081 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122424785 | ATGAAGTAAGAAAAG[G/T]TCTCACAGGGACGAA | 93664 |
rs201600144 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122658555 | AAATACTATGCAGCC[A/G]TAAAAAAGGATGAGT | 93664 |
rs201602983 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122827632 | AGCGAAATTCCATCT[A/C]AAAAAAAAAAAAGAA | 93664 |
rs201603130 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122513291 | CCATCTTTTCCAAAC[C/T]TTCTGTCCAAGGGCA | 93664 |
rs201604072 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122719888 | ATTAGGGAAAGAAAA[A/C]CTACCTCTCTGCAGT | 93664 |
rs201604739 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122626240 | GAACATCACTGGCTG[G/T]TGTGTTAATGAGGAC | 93664 |
rs201619071 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122427180 | TTCTTTTTTAGAAGA[C/T]ACATATCCACCAGAC | 93664 |
rs201627596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122429900 | TTTTTTTAATAAACA[C/T]GTGGCCTCTAGACAC | 93664 |
rs201630707 | snp | A/C | 0.000166061 | 0.00911058 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122701900 | AGCCAGGGGTCAATG[A/C]ATGCCTTATGGAAAA | 93664 |
rs201631195 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122821077 | GTCTCCCACAATTAC[C/T]GTTGTTCCTGGCCCA | 93664 |
rs201650038 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122405667 | CTGTCTCAAACAAAA[A/C]AAACAAAAAACCGGC | 93664 |
rs201650811 | snp | A/C | 0.000236696 | 0.0108762 | intron-variant | CADPS2 | GRCh38.p7 | 7:122387222 | TTCTGCTATACAGCT[A/C]ACCTGTTTTGTAAAA | 93664 |
rs201668378 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122744539 | ATAAACTTGCCCCAG[A/C]GAACAGTGAACACCT | 93664 |
rs201670657 | in-del | -/T | 0.0256215 | 0.110247 | intron-variant | CADPS2 | GRCh38.p7 | 7:122448121 | TCTTTTAAAGTTTTG[-/T]TTCACTGTCTGACAC | 93664 |
rs201685005 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122821045 | TGGCTCCTTCAGCTA[C/T]ACTCACTCTTTGTTG | 93664 |
rs201686419 | in-del | -/GA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122367296 | TGAGAGAGAGAAAGC[-/GA]GAGAGAGAGAGAATG | 93664 |
rs201688189 | in-del | -/CT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122356506 | CCCCATCTTCCTTTG[-/CT]TATTGTACTCTTCGG | 93664 |
rs201689558 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122678877 | GAAACCATGGCAGAA[C/G]ATAAATTGTGAAGAT | 93664 |
rs201690760 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122729699 | TTTTTTTTTTTTTTA[C/T]TGTTGAGTCCTTTGA | 93664 |
rs201703729 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122588911 | AGTGAGTTGATCAGA[A/C]AGGCCTGATGGTATT | 93664 |
rs201706153 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122817330 | TTTAAATCAGGTAAG[C/T]GGCCTCTTCTTATTC | 93664 |
rs201706404 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122621115 | CTATGTTGCCTAGGC[G/T]GGTCTTAAACTTCTT | 93664 |
rs201725527 | in-del | -/ACAC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122366611 | CTCCATCTCAAAAAT[-/ACAC]ACACACACACACACA | 93664 |
rs201728403 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122666347 | TGTGTCTGCTAACAC[-/T]TTTTTTTTTTTTTTG | 93664 |
rs201752069 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122614131 | GTGTATGAGGGACTG[C/T]ATGAAGTCCAGGGTG | 93664 |
rs201752293 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122433407 | GTTTTTTTTTTTTTT[-/T]GAGATGGAGTTTTGC | 93664 |
rs201755681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122468597 | AATCAATACTGATAG[C/T]ATTTTATAATGATGT | 93664 |
rs201760067 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122520344 | GTTGAATGTGTGTGT[-/G]TTTTTTTTTAAGTAG | 93664 |
rs201768126 | in-del | -/TATTT | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122697167 | CTTAAAGAGTGCTAG[-/TATTT]TATTTTAAAATTTCA | 93664 |
rs201796821 | in-del | -/TATA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122645489 | TATATATATTTAGCG[-/TATA]TATATATAAGTATAT | 93664 |
rs201815806 | in-del | -/CATTTA | 0.030278 | 0.119257 | intron-variant | CADPS2 | GRCh38.p7 | 7:122577458 | GACTTCTTCCATTTG[-/CATTTA]CATTTACATTCGTCT | 93664 |
rs201820529 | in-del | -/T | 0.0368353 | 0.130617 | intron-variant | CADPS2 | GRCh38.p7 | 7:122801757 | AAAGCCAAGAGAATC[-/T]TTTTTTTTTAATTTT | 93664 |
rs201823931 | in-del | -/G | 0.0142736 | 0.0832652 | intron-variant | CADPS2 | GRCh38.p7 | 7:122667432 | GAAACTTACATTTTT[-/G]AACTCATTTCCCCTA | 93664 |
rs201827445 | in-del | -/A | 0.0123036 | 0.0774623 | intron-variant | CADPS2 | GRCh38.p7 | 7:122749714 | CCAAATTTTAGTGGC[-/A]AAAAATGCCATGCTA | 93664 |
rs201832092 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122635938 | TCCCACATTTTTTTT[G/T]GTTTTCCATTTGCAT | 93664 |
rs201842473 | in-del | -/TC | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122828369 | TTTTTATCCACTCTA[-/TC]TCTGTTTTTTGTAAG | 93664 |
rs201845842 | in-del | -/TA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122662395 | TTTTTTTTTTTTTTT[-/TA]AGACGAGTCTTACTT | 93664 |
rs201850059 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122679069 | TGAACAATATGAAAT[A/C]TGGGCACCTTAAGAA | 93664 |
rs201855753 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122713317 | AAATCCTGTACTTAA[A/C]ACTAGCTCTACAACT | 93664 |
rs201863739 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122428469 | TATATATATATATAT[A/T]TATTTTTTTTTTTTT | 93664 |
rs201867666 | in-del | -/AT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122706789 | TGTGTGTGTACATAC[-/AT]ATATATATATACACA | 93664 |
rs201869950 | snp | A/G | 3.47192e-05 | 0.00416634 | intron-variant | CADPS2 | GRCh38.p7 | 7:122438477 | AACCTACAGAGAGAG[A/G]AAGTGGAAGGGTGAG | 93664 |
rs201882161 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122656109 | GAATATTTACTTGTC[C/T]AGTAATTTTGAAAAA | 93664 |
rs201882662 | snp | A/G | 1.66065e-05 | 0.00288149 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122474444 | GAGTATTCTAAAAAG[A/G]AAGGCATGATCAAGC | 93664 |
rs201882927 | in-del | -/ATATAT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122708462 | TATATATGTGTGTGG[-/ATATAT]ATATATATATATATA | 93664 |
rs201885600 | in-del | -/TT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122642549 | GTTTCACCCAACAGC[-/TT]TTTTTTTTTTTTTTT | 93664 |
rs201915652 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | CADPS2 | GRCh38.p7 | 7:122319933 | AAACTACACAAAAGA[A/G]GATGCTCTTCTCCAA | 93664 |
rs201918522 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122596240 | TCAAGAACATTTAAG[C/G]TCATTTTGTTAGAAA | 93664 |
rs201924211 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122463320 | AAAATCTTCATATTC[A/T]TAGATTTTTTTTTTT | 93664 |
rs201947423 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122869567 | ACTAGACCTGCTTTA[G/T]AAAAAAAAAATGCTA | 93664 |
rs201959382 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122721755 | AAAGAGAATTTTACA[C/T]CAATATCCCTGATGA | 93664 |
rs201966263 | in-del | -/T | | | intron-variant, nc-transcript-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122531164 | TTATATTCTTTGTGA[-/T]TACTTTCTCATTTGT | 93664 |
rs201973741 | snp | A/G | 0.000132503 | 0.00813842 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122702311 | GCGACTATATTTTCC[A/G]TCCCCTGGTGAGACA | 93664 |
rs202000609 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | CADPS2 | GRCh38.p7 | 7:122681045 | CAAAAAACCAAACAC[C/T]GCATATTCTCACTCA | 93664 |
rs202008854 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122645240 | CGCTAAGTATATATA[C/T]ACACACATGTACATG | 93664 |
rs202010822 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122501899 | AAAAAAAAAAAAAAA[A/G]GAAAAAAAAAGTCAC | 93664 |
rs202011469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122820621 | CTGGAGTGCAGTGGC[A/G]CGATCTCGGCTCACT | 93664 |
rs202022394 | snp | C/T | 2.17224e-05 | 0.00329556 | missense | CADPS2 | GRCh38.p7 | 7:122491402 | TATAACTGCACATAG[C/T]AAAGGTATATTGGCT | 93664 |
rs202023339 | in-del | -/T | 0.00795532 | 0.062565 | intron-variant | CADPS2 | GRCh38.p7 | 7:122860540 | CCCAGCCATAATATA[-/T]TTTTTTTTAAAGATA | 93664 |
rs202028705 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122696518 | CCCCATGGTCATGGA[A/G]GCAGTTATAGCTAAC | 93664 |
rs202039633 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122564836 | ACACAGACACACACA[C/T]ACACACACATGCACA | 93664 |
rs202040015 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122347286 | AGAGAGTTCTTGCCA[-/T]TTTTTTTTTGGAGGG | 93664 |
rs202044024 | in-del | -/TCTT | 0.0356815 | 0.128715 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122700578 | ACAACAATACCTAAA[-/TCTT]TCTGTCTCTCATTGT | 93664 |
rs202050897 | snp | A/G | 4.97146e-05 | 0.00498546 | intron-variant, synonymous-codon | CADPS2, RNF148 | GRCh38.p7 | 7:122702436 | ACAGCCTCCACGTTC[A/G]ATGAGGGCCAGCCAT | 93664 |
rs202051694 | snp | A/C | | | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122325546 | TCTATCAGTCAACCA[A/C]ACGCAAATGACTTTC | 93664 |
rs202056065 | in-del | -/T/TT | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122744981 | TTTCTTTTTTTTTTT[-/T/TT]ACTTTATTGAACTAT | 93664 |
rs202059753 | snp | A/G | 0.000169986 | 0.00921759 | intron-variant | CADPS2 | GRCh38.p7 | 7:122615161 | CAACAACAATAATAC[A/G]CTTTTTTCAACTGGC | 93664 |
rs202081303 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122411472 | TAATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT | 93664 |
rs202082907 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122410727 | AGTAATTACAAATAT[A/G]TGTTGACTACCGCAA | 93664 |
rs202085929 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122671646 | TCTTGTGAGAAGCAG[-/C]TGATCAACTGCCCGG | 93664 |
rs202086373 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122625055 | TGATGATTAATTATT[-/A]TTTTTTTTTTTTGAG | 93664 |
rs202089315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122725512 | CCCAAATAGTGTACA[C/T]GTACCCAATAGGTAG | 93664 |
rs202096344 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539744 | GCCTGTCTGTCCCTC[C/T]CTCTCTGTCTCTCTC | 93664 |
rs202107182 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122666046 | TCAACCTCATCTAAT[C/G]ACTCATTGAGCAGTG | 93664 |
rs202130097 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122583819 | ACATCATATACATAT[-/G]CATATGTATATTCAT | 93664 |
rs202133457 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122794749 | AAAGAACTGAAATCA[-/T]TTTAAAAAAAAAAAA | 93664 |
rs202134947 | in-del | -/AT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122645385 | TACACACATATGTAC[-/AT]GTGTGTGTATATATG | 93664 |
rs202140194 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122726773 | AAGAGCTTCCTGATA[A/C]AAAAAAAAAAAAAAA | 93664 |
rs202141735 | snp | C/T | 0.00013287 | 0.0081497 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122701981 | AAGCAAACAACACAG[C/T]TGTCTTCATTTAGGT | 93664 |
rs202142579 | in-del | -/AG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122725905 | ACGCCTGGATGACAC[-/AG]CTCACAGATAGCAGA | 93664 |
rs202143400 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122869169 | AAAACTGCCCAAGTC[A/T]AGGGAAGAAATTAGA | 93664 |
rs202153493 | snp | C/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539761 | TCTCTGTCTCTCTCT[C/G]TCTCTGTCTCTCTCT | 93664 |
rs202155427 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122367539 | TAAACCTTCCCCCAG[-/C]TTTTTTTTTTTTTTT | 93664 |
rs202173368 | in-del | -/T | 4.26903e-05 | 0.00461989 | intron-variant | CADPS2 | GRCh38.p7 | 7:122360856 | TAATCATGAGAATTA[-/T]TTTTTTTAACTGCCA | 93664 |
rs202200728 | snp | C/T | 0.000399062 | 0.0141199 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122702077 | GTCTTTATTTGACTT[C/T]GCCTCCTGGTGAAAG | 93664 |
rs202206889 | in-del | -/AAAT | 0.442113 | 0.159977 | intron-variant | CADPS2 | GRCh38.p7 | 7:122878640 | GCAAGACTCTGTCTC[-/AAAT]AAATAAATAAATAAA | 93664 |
rs202215835 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122756689 | GCATCACCTGAGGTC[A/G]GGAGTTCGAGACCAG | 93664 |
rs202232252 | in-del | -/AAAG | 0.00676609 | 0.0577691 | intron-variant | CADPS2 | GRCh38.p7 | 7:122768965 | TTATCAGAAAAAAAA[-/AAAG]AAAGAAACGGTCACA | 93664 |
rs202233674 | in-del | -/ATAC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122760000 | TATATATATATATAT[-/ATAC]ACACACACACACGGC | 93664 |
rs202233764 | in-del | -/TTT | 0.480302 | 0.0972668 | intron-variant | CADPS2 | GRCh38.p7 | 7:122493721 | TGGTTATGTTTAATC[-/TTT]TTTTTTTTTTTTTTT | 93664 |
rs202238707 | snp | A/C | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122562694 | TTTTAAATTTCTCCT[A/C]ATAAGTGTGTGATTT | 93664 |
rs202240049 | in-del | -/ACTG | 0.0260105 | 0.111035 | intron-variant | CADPS2 | GRCh38.p7 | 7:122757702 | GAGTTTTTTAAAACA[-/ACTG]ACTAACAGCTACTAG | 93664 |
rs202241255 | snp | A/T | 0.151334 | 0.229706 | intron-variant | CADPS2 | GRCh38.p7 | 7:122669357 | TATATATATATATAT[A/T]TTTTTTTTTTGAGAA | 93664 |
rs207468520 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122384487 | GGCTCACCTGTATAT[A/G]TAATGTATATACTAA | 93664 |
rs207468521 | snp | C/G | | | missense | CADPS2 | GRCh38.p7 | 7:122471472 | GTTCCATCAGTTCTG[C/G]AAGGTAGCAGAGATG | 93664 |
rs207468522 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122665302 | CACCACTTTAGTTCT[A/C]CCTCTTAAGGTCACT | 93664 |
rs207468523 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122783211 | AAAAAAAAAAAACAA[A/C]AACAAAAAAACCAGC | 93664 |
rs207468524 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122783935 | GGCCTTCCAAGAGGG[C/G]TTGCGGCTATTACTA | 93664 |
rs207468525 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122858584 | TCAGTTAATCACACT[C/T]ACTTCTTTTAAAAGC | 93664 |
rs207468526 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122866349 | TCTACTCTTGCCCCT[A/T]CAATCTATTCTCAAG | 93664 |
rs267601255 | snp | C/T | | | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698474 | TAACCACAACGACAT[C/T]TTCAAATGCCTGATG | 93664 |
rs367546556 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122692168 | AACGTCCTTCTCCTG[A/G]ATGACTTGCACTAAG | 93664 |
rs367547405 | snp | A/C | 0.000167986 | 0.00916322 | missense | CADPS2 | GRCh38.p7 | 7:122416133 | AAGAATCTCTTCCAG[A/C]TTTCTAGCAGGAGAT | 93664 |
rs367553493 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122734387 | AAAAAAAAAAAAAAA[-/G]AAAAAAAAAAAAGAA | 93664 |
rs367561271 | snp | A/G | 2.01051e-05 | 0.00317052 | intron-variant | CADPS2 | GRCh38.p7 | 7:122490037 | ATTTTATATCTTATT[A/G]AGGCTATTAATTGAT | 93664 |
rs367565266 | snp | A/G | 0.000118416 | 0.00769377 | intron-variant | CADPS2 | GRCh38.p7 | 7:122621466 | CAGAGGTGAGCATGA[A/G]ATAAAGCTACTTACC | 93664 |
rs367567195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122422383 | ACTGTCAGCCTACTC[C/T]TGTGGACTGCTTGCT | 93664 |
rs367569835 | snp | A/G/T | 0.000231851 | 0.0107645 | intron-variant, stop-gained, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122702254 | ACTCCTTTCTGAATC[A/G/T]AGTGCAAAATTTCCA | 93664 |
rs367588502 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122814036 | AGTCATGTTATCCCC[A/G]TTTTATAGCTAAGTA | 93664 |
rs367591903 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122831359 | AATGTAACCCTATGT[A/C]ATTTGTACCATAAAA | 93664 |
rs367608032 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | CADPS2 | GRCh38.p7 | 7:122839873 | GGAAGACAGTGTGGC[A/G]ATTCCTCAAGGATCT | 93664 |
rs367617404 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122821445 | CTACACATCAAGCTC[A/G]AGGATTTGCCCCACC | 93664 |
rs367631717 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122469889 | GACAAAGGTAATGAG[A/G]TAAGTACAGACAAAA | 93664 |
rs367641321 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122829687 | CATGTATTAAGTGTG[C/T]TTTAGAACCACTGTA | 93664 |
rs367647400 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122397250 | TACCTATATTTCCTA[C/T]GAACTACAAAAAATC | 93664 |
rs367651679 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122482456 | CAAATAATTATCTAG[C/G]CCAAAATGTCAATAG | 93664 |
rs367671935 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122828358 | GTTCCTTTTTTTTTT[-/T]ATCCACTCTATCTCT | 93664 |
rs367672170 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122879340 | CAGGAGTTCGAGACC[A/T]GCCTGGCCAATATGG | 93664 |
rs367676340 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122578570 | CTCAGCAGATCTAGA[A/G]TGGGGTCTGAGAATT | 93664 |
rs367677226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122640890 | AGTGAGCCGAGATCA[C/T]GCCACTGCACTCCAG | 93664 |
rs367680248 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122354319 | GTGTAATTACATCTC[C/T]ATTTTACAGAAGAAG | 93664 |
rs367680702 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122549488 | TAGCCAGGTGTGGTG[A/G]TGCATGCCTGTAGTC | 93664 |
rs367686702 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122645458 | ACACACACATATGTA[C/T]ATATGTGTATATATG | 93664 |
rs367701027 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122622127 | AGCTTTCCAAGTTAG[A/G]AAACAAACATTTTAA | 93664 |
rs367731443 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122783559 | CTGACACACAGATAT[C/T]CTGTTTTGCCAGTCC | 93664 |
rs367737874 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122870445 | GAAACAGAGTAGAAA[C/G]ATAGCCACCAGAGGC | 93664 |
rs367755841 | in-del | -/AT | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122844442 | AATCACCTAAACGAC[-/AT]ATCTTTTCAATCACT | 93664 |
rs367777074 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122325327 | TATTCATTTATTAAT[C/T]TAACTAAACGTGGAA | 93664 |
rs367782207 | in-del | -/AAC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122881319 | AAAGAAGCAAATGAC[-/AAC]GTCACTTAATCTGTC | 93664 |
rs367784930 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122474709 | TAAAAACAACAGCAA[A/C]AAATCTACAAATCAT | 93664 |
rs367787132 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122342192 | TGACTTATTATTGGA[A/G]ATGGGAATGATAGCA | 93664 |
rs367799601 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122673195 | CAGCAGCAAGATTCA[C/T]TGCAAAGAGCGAAAG | 93664 |
rs367812049 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122656857 | GACGCCATTGCTTCT[A/G]GTGTTTTAGACATGA | 93664 |
rs367823491 | in-del | -/GTGCTCATATCATGAC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122484902 | TGCTCATATCATGAC[-/GTGCTCATATCATGAC]TGTTTCATGTTATGG | 93664 |
rs367828313 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122720163 | AAAAGTGTCAATCAG[A/G]CCTAACGAGTCATTC | 93664 |
rs367839214 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122356828 | AGTTTTGTGTTTTTT[-/T]GTGAACATCTCCTTT | 93664 |
rs367852004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817493 | CAAAACTCTGGCGCC[A/G]GTCACAGACTGGGAA | 93664 |
rs367852174 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122756419 | CATTATCAAAAGAAA[C/T]GTATACAACCACATT | 93664 |
rs367858417 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122352162 | TGCTAATACAGTAGC[A/G]CCAAACACAAAATGT | 93664 |
rs367867153 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122422920 | GCCGAGATCGCGCCA[C/T]TGCACCCCAGTCTGG | 93664 |
rs367883569 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122719968 | GGAAAGAACTTGCTC[A/G]ATAAAGAGTTATTGG | 93664 |
rs367899406 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122366648 | ACACACACACACACA[C/T]ATATATACATACACA | 93664 |
rs367909968 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122637058 | ATTGTTTATTTATTT[C/T]TTTCTTTTTGTCTGA | 93664 |
rs367911556 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122747563 | CAGCACAATTCTAAC[C/T]TCTTTACATAGATTA | 93664 |
rs367912699 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122394130 | ATTTTCTTTTTAGTC[A/G]TTCAATTTTGCATAT | 93664 |
rs367912862 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122551795 | AAATGATTGACAAAA[C/T]ACGATCCAGGCCCAA | 93664 |
rs367915933 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122569632 | CCTGACTTCAAACTA[C/T]ACTACAAGGCTACAG | 93664 |
rs367916870 | in-del | -/AAATAAATAAAT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122878640 | GCAAGACTCTGTCTC[-/AAATAAATAAAT]AAATAAATAAATAAA | 93664 |
rs367920635 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122547386 | TTCTGGGGCAATAAT[A/G]TTTTGAAACACACTC | 93664 |
rs367928494 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122476875 | ATTTCATGCAAAACT[A/G]CATTACCATGTGGCA | 93664 |
rs367931611 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122783174 | TGAGCCGAGAGGCGA[C/T]AAAGCGAGACTCCAT | 93664 |
rs367931777 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122453193 | TCCATCTGAATGCAT[C/T]TTGAATGTTAACTAT | 93664 |
rs367953991 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122869795 | ACACAAACAGTAAAA[G/T]ATACAAAATATGTCA | 93664 |
rs367959371 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122359642 | TATCAAACATAAAAT[C/T]TCCCCTTAATTCTCC | 93664 |
rs367961996 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122495165 | TAAAGAAAAGTACAA[C/T]AATACACTAACATGT | 93664 |
rs367971310 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122333703 | CCTAGAACTCTATAC[A/G]GGTGTCTATAAAAAT | 93664 |
rs367971931 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122817546 | ATCATTGCAGGGACG[A/C]CTCTCTGATTATTCA | 93664 |
rs367982294 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122544071 | AGCTCAGCAGTTCCA[C/T]TCCTACGTGTCCACT | 93664 |
rs367987900 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122753768 | TTGTATACATATAAA[C/G]ACACGAACGCTTGCA | 93664 |
rs367993861 | snp | C/T | 0.000169985 | 0.00921758 | synonymous-codon, utr-variant-5-prime | CADPS2 | GRCh38.p7 | 7:122621655 | CAAATTCACTGAAGA[C/T]CGCAACTCTTCTATA | 93664 |
rs367996976 | snp | C/T | 0.000181984 | 0.00953723 | intron-variant | CADPS2 | GRCh38.p7 | 7:122480847 | AAAATCATGAAAATA[C/T]TTACCTTTACCAGCT | 93664 |
rs368001118 | in-del | -/ATTA | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122737128 | GAAAAAATAATGACT[-/ATTA]AAAATCATATTTGCT | 93664 |
rs368001145 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122532534 | CCGACCTCTCCCCAC[A/C]CCCACCCCCCTACCC | 93664 |
rs368023665 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122858368 | AATAGAGCTTTTATA[C/T]AAGAAACAAAGTTCT | 93664 |
rs368037775 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122351145 | CTGAGGTGGGCAGAT[C/T]ACGAAGTCAGGAGAT | 93664 |
rs368038140 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122705959 | TAATATATAATATAT[-/A]ATATAATATAATATA | 93664 |
rs368043420 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122561223 | TATTTTCAAAGCTGG[A/G]AAGAATTTTGGAATT | 93664 |
rs368045673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122636985 | CAGGAATGCCAATGA[A/G]TTGTAGATTTGGTGT | 93664 |
rs368047421 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122887892 | CAGGCCCCCTAGTAA[C/T]AAAAGGTCTTCAGTA | 93664 |
rs368049014 | snp | A/C | 0.000161987 | 0.00899818 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122702372 | AGTTGTAGATGATCA[A/C]CCCATTTGCTCCCTT | 93664 |
rs368054434 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122490636 | TTGCCATTCTATACA[C/G/T]GGGAAAAATATATAA | 93664 |
rs368060010 | in-del | -/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122552775 | TATGATAGGTTCCTG[-/T]TTTTTTTTTTTTTTT | 93664 |
rs368064094 | in-del | -/GGAA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122644118 | GAAGGAAGGAAGGAA[-/GGAA]CAAACGAAGGAAAAG | 93664 |
rs368064829 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122518509 | CTTCATAAAGTATGA[A/G]TCTACCAAATAAACA | 93664 |
rs368066059 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122847983 | CAAAAGAAAACTAAT[C/T]TTCTAGAGCAACTGC | 93664 |
rs368069768 | in-del | -/TTTT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122442791 | TCACTCAAGTTTTTT[-/TTTT]AACAGAATATCACAT | 93664 |
rs368074922 | snp | A/G | 3.31511e-05 | 0.0040712 | intron-variant | CADPS2 | GRCh38.p7 | 7:122393335 | AAAGAAACAAACAAC[A/G]TGGGAAGGGACCACC | 93664 |
rs368078375 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122672599 | CACCTCCTGGGAGAA[A/T]AGAGACAGAATACTG | 93664 |
rs368078936 | snp | C/T | 3.56818e-05 | 0.0042237 | intron-variant, utr-variant-3-prime | CADPS2, RNF148 | GRCh38.p7 | 7:122701830 | GAAAATTCTCCAGAT[C/T]TCTTAAGTTTTCAGG | 93664 |
rs368087636 | snp | A/C | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554761 | GAACTAAAATATTTT[A/C]TATGTTTTCCTGTTT | 93664 |
rs368091427 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122656413 | AGCCCTCTTGACTCA[C/T]GTACTGAAAAGCAAA | 93664 |
rs368095522 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122738804 | TGTAGCTGGGAGTAA[C/T]AGACTGATTTAAAAA | 93664 |
rs368102277 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122664409 | AATTGTCCATTACTA[C/T]TGGAAAATAAAATAA | 93664 |
rs368102356 | snp | C/T | 1.85033e-05 | 0.00304159 | intron-variant | CADPS2 | GRCh38.p7 | 7:122471354 | CCATACATTTCACTT[C/T]GTATTTGCAAGTAAA | 93664 |
rs368103158 | snp | A/T | 0.158302 | 0.232576 | intron-variant | CADPS2 | GRCh38.p7 | 7:122705904 | ATATAATATAATATA[A/T]AATATATTATATAAT | 93664 |
rs368108992 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122589228 | AATATCCCACCTTTA[C/G]TAATAAACAGTATTA | 93664 |
rs368114197 | snp | C/T | 6.9389e-05 | 0.0058898 | missense, utr-variant-5-prime | CADPS2 | GRCh38.p7 | 7:122663550 | ACCATTCTGGCCACT[C/T]GGTCACTCTTTAGAA | 93664 |
rs368118247 | snp | A/C | 0.000167986 | 0.00916323 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122702740 | GAAGGGGTAATTCTA[A/C]GGAAGCTCATGCCTC | 93664 |
rs368124248 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122453756 | TAAGTTGTCCTATCA[A/T]ATTAGATTTCACTGA | 93664 |
rs368124428 | snp | C/T | 1.68258e-05 | 0.00290045 | missense, intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554587 | GTTTATCCATTCGCA[C/T]TGCCAGTTTGATTTT | 93664 |
rs368135986 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122428594 | TGCTTCAGCCTCCCG[A/G]GTAGCTGGGACTACA | 93664 |
rs368144489 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122697928 | TCTCCTCTTCACTAG[A/G]TGATAAGGTTTCAGG | 93664 |
rs368150182 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122403887 | CAAAACTTCCAAGAA[A/T]TCCACAACATATTTT | 93664 |
rs368173738 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122638332 | CGTCCTCCCCACCCC[C/G]TGCTTGGGGCTCTGC | 93664 |
rs368175774 | snp | A/G | 6.62482e-05 | 0.00575497 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122393491 | GTGAATTGACTGGGC[A/G]ATGGAAGACTCCATG | 93664 |
rs368178948 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122476456 | AATGTTTCTGAAAAA[C/T]GATCTATAGTTCATT | 93664 |
rs368184707 | snp | A/C/G | 3.65987e-05 | 0.00427765 | intron-variant | CADPS2 | GRCh38.p7 | 7:122451497 | AAAAAATCAGAATCA[A/C/G]TAATTCATATTGATC | 93664 |
rs368198500 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122739931 | CTATATAGCAACTCA[A/T]ATCAGTAGTAATGGA | 93664 |
rs368198874 | snp | A/G | 7.38798e-05 | 0.00607737 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122702722 | GAAACAGAACTATGC[A/G]TCGAAGGGGTAATTC | 93664 |
rs368211686 | in-del | -/CACA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122564848 | ACATACACACACATG[-/CACA]CACACACACACACAC | 93664 |
rs368213630 | snp | C/G | 0.295599 | 0.245806 | intron-variant | CADPS2 | GRCh38.p7 | 7:122822601 | CCCCTGTGACTTGCA[C/G]GTATATGCCCAGATG | 93664 |
rs368216153 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122797963 | ATTTTGAGTTATACA[A/T]GTTTATTTAATATTT | 93664 |
rs368217399 | snp | A/G/T | 0.000179252 | 0.00946539 | intron-variant | CADPS2 | GRCh38.p7 | 7:122325624 | AGGAGAACAAAAAAA[A/G/T]AAAACAACCTCTGCA | 93664 |
rs368228928 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122684077 | TTTATTAAATGTATA[A/G]AGAGCTCACATTTAT | 93664 |
rs368234721 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122534046 | AGGCACATCACATTC[A/G]ACTCCTTTATTATCC | 93664 |
rs368235743 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122560080 | AAAAAGTTTAGTTGC[A/G]GCCAGATAGCAATGG | 93664 |
rs368240415 | snp | A/C | 0.000165986 | 0.00910853 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122663471 | TGGCAAACTCCGCAC[A/C]CGTTTTTCTATGTTT | 93664 |
rs368252649 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122860231 | CAACAAGTACCTGAC[A/G]CAACATTTTTTTTTT | 93664 |
rs368258128 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122769931 | TTCATTACAGCTAAT[A/G]TTTACTGAGCACTTT | 93664 |
rs368274150 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122768986 | AGAAACGGTCACAGC[C/T]GTCAGATCTATATTT | 93664 |
rs368275718 | in-del | -/ACAC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122774270 | GACATAGATAGATAT[-/ACAC]ACACACACACACACA | 93664 |
rs368276745 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122836882 | AACGAGACAGAAAGT[C/T]AACAAGGATATCCAG | 93664 |
rs368277516 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122857045 | TCATCATGGCACAAA[C/T]TATGATTTGTATGTA | 93664 |
rs368285604 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122496949 | TCTGTGGATTCTTCA[C/T]GCAATTCTCTTAAAT | 93664 |
rs368286311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122320785 | GTGTGGAGGAAGAAG[A/G]TTAATCCTATTATCG | 93664 |
rs368294829 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122464051 | TGTCACCTAGATCTT[A/C/G]GTTTCTAAATACCAT | 93664 |
rs368298318 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122565588 | GAATCCTGCTCTTCT[A/G]ATCTAAGGAGTTCTT | 93664 |
rs368306778 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122543356 | CAAGTAATTAGCTCT[A/G]CTGTATCTAATGCAT | 93664 |
rs368308978 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122546792 | AGTCCATTCCTCTCC[A/G]TATACAGTCTAGGAC | 93664 |
rs368311665 | snp | C/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539771 | TCTCTGTCTCTGTCT[C/G]TCTCTTTCTGTTTCT | 93664 |
rs368316478 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122846357 | ACAAGAAAATCACTG[C/T]AAATACTTTACAAAT | 93664 |
rs368343965 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122705549 | TATATTATATATTAT[A/C]TATATTTATATTATA | 93664 |
rs368351432 | in-del | -/TAAC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122791637 | GCTATTTAATAACAC[-/TAAC]CATGGCAACACAGGA | 93664 |
rs368372675 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122588281 | TTTATCATGAAATCT[C/T]TGCCTAAATGGTATT | 93664 |
rs368373179 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122679023 | TAATGACTGCGTTAA[C/T]TGCACAAATTGTTCG | 93664 |
rs368373800 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122503707 | TTATAAGTACTTTTT[C/T]CCTCCCTCTCATTCA | 93664 |
rs368376881 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122526489 | TGAGCCATCCCGCCT[A/G]GTCTTCTTTGATATT | 93664 |
rs368381865 | snp | A/G | | | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122701120 | CATGGCTAATTCTCT[A/G]TGGCAATGTCACAAT | 93664 |
rs368385359 | in-del | -/A | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122549348 | AATTAATACAAAAAA[-/A]TCAAGGATTGATAAA | 93664 |
rs368389417 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122363887 | TGGTCCTTAAGCTAA[C/T]GGGTCTAATTCAATT | 93664 |
rs368390474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122806607 | TATCTTTCTCTCACA[A/G]CTTAACATTAATGCA | 93664 |
rs368393725 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122434733 | TAAAAAATTCAGCGA[C/T]TCAGCGAACTCTTTC | 93664 |
rs368398356 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122411478 | ACCCGCCTCAGCCTC[C/T]CAAAGTGCTGGGATT | 93664 |
rs368411305 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122430218 | CCATGCTACCTTTTG[A/T]TCAGGGCACCTCCAC | 93664 |
rs368414253 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122427733 | GTCTTAGATAACACT[A/T]TTTTTTTTCTAAGTT | 93664 |
rs368426331 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122373757 | TCAAAAACCTCTCAA[C/T]AAAGAAATGGCTTCA | 93664 |
rs368434379 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122705760 | AATATATATAATATA[A/T]AATATATGATATATT | 93664 |
rs368437683 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122533487 | CAAATCAACAAACTC[A/G]CACTGCTTAACGGAA | 93664 |
rs368441756 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122583574 | CACATAAATATATCA[A/G]AATATATGTGTGTGT | 93664 |
rs368445964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122573817 | TGTCTAAAATGACTA[C/T]GTATAAAAATACTTT | 93664 |
rs368455926 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122501608 | TAATCCCAGCACTTT[A/G]GGAGGCCGAGGCAGG | 93664 |
rs368458971 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122455282 | TGCACACCTGGCTTG[C/T]TTGCTCACTTTCTTC | 93664 |
rs368466186 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122694665 | CACTCCCTTCCCCCC[-/C]ACTTATAAAACCAAG | 93664 |
rs368466216 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122691655 | GTGACACTATGAAAG[C/T]CCATTGTCACCCTCC | 93664 |
rs368482034 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122470750 | ATCCACCCTCCTTGG[C/T]CTCTCAAAGTGCTAA | 93664 |
rs368506136 | in-del | -/TACATT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122577468 | ATTTGCATTTACATT[-/TACATT]CGTCTATGCCACTGC | 93664 |
rs368507294 | in-del | -/TCT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122663046 | AAGTACTGATATTCT[-/TCT]CCTTCTACCAAATAC | 93664 |
rs368511706 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122363758 | AAATGTAAAGAATTA[A/G]TATTATCCATATGAT | 93664 |
rs368513084 | snp | C/T | 0.000131245 | 0.00809971 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554719 | AAACCCACATTTAAA[C/T]GCATGATACGGAGTG | 93664 |
rs368514594 | snp | A/G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122404319 | CCCTACAAAGGACAT[A/G/T]AACTCATCATTTTTT | 93664 |
rs368528830 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122441067 | ATTGAAAGAAATTCT[A/G]AGATGAATATTGAAT | 93664 |
rs368533164 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122357085 | CTGTTAAATGTAACC[A/C]GCTCTATCTGTACTA | 93664 |
rs368540236 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122580257 | GTCAGGAGTTCAAGA[C/G]AAGCCTGGCCAAGAT | 93664 |
rs368543202 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122601916 | AGTCTCCCTTTTAAA[C/T]GGGAAGGCTTAGAAA | 93664 |
rs368577585 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122492948 | CTTTTTCTGTTTTTA[A/C]ACATAAAATGAAACT | 93664 |
rs368581599 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122815101 | ATCTAAAGAAAAGAG[A/G]TTTAACAAAACAGAG | 93664 |
rs368588577 | snp | A/G | | | intron-variant | CADPS2, RNF148 | GRCh38.p7 | 7:122701226 | TACGATTAAGAAAAT[A/G]TGGCACATATACACC | 93664 |
rs368591458 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122806123 | ATGTGGCAGTCACAA[C/T]AGATGAGACTCACAT | 93664 |
rs368592516 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122762166 | CTCAATAGAGGCGTT[A/G]GAAGATAAAGTTCAA | 93664 |
rs368592864 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122790907 | TCTCAACACTAATGG[A/T]TGTAGGAATATTAAC | 93664 |
rs368597229 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122745728 | ATATCAGTTGGTTGC[C/T]ATGAAACTATTCCCT | 93664 |
rs368612323 | snp | A/C | 9.5288e-05 | 0.00690181 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122441527 | CCTTTCAAGTAATGA[A/C]AGTGTAGCTTTTAGA | 93664 |
rs368612600 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122839120 | AGCCCTCAGAAATAA[C/T]ACCACACATCTATAA | 93664 |
rs368630763 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122612671 | AGCTGGTAATCTTTG[A/C]ATAATCTTTACAAAA | 93664 |
rs368632624 | snp | A/G | 4.98824e-05 | 0.00499387 | intron-variant, synonymous-codon | CADPS2, RNF148 | GRCh38.p7 | 7:122701893 | GGCTAAAAGCCAGGG[A/G]TCAATGCATGCCTTA | 93664 |
rs368634874 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122579720 | GTCTCCAAAGCTCTT[C/G]TATTAGATTATGCTA | 93664 |
rs368636743 | snp | A/G | 1.9054e-05 | 0.00308652 | missense | CADPS2 | GRCh38.p7 | 7:122451381 | ATATATACCTGAAAT[A/G]GCTTATCTGATTTTC | 93664 |
rs368653836 | snp | C/G | | | intron-variant, upstream-variant-2KB | CADPS2, LOC105375481 | GRCh38.p7 | 7:122528659 | TCCATTTATTTATTT[C/G]CTGACAAAACTATAT | 93664 |
rs368667467 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122727479 | CTTTTTTAAGAATAT[A/C]CAAGCAGAAGAAAAG | 93664 |
rs368685078 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122813499 | GTGTTTATAGTTCTC[C/T]AGTCAAAAACCATTC | 93664 |
rs368690671 | in-del | -/AG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122877688 | TTCAAAAAGTTACAG[-/AG]TCTTGACTAATTGAA | 93664 |
rs368719335 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122669816 | TCACATCTCTCCTTA[A/G]GTGTCCCACTGGCAC | 93664 |
rs368728397 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122424791 | TAAGAAAAGCTCTCA[A/C]AGGGACGAATATATC | 93664 |
rs368728520 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122838380 | GGCACAAACAGGGAT[G/T]CCCTCTCTCACCATT | 93664 |
rs368731435 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122735934 | AAGGTGAAATCTAAG[G/T]TCCTATAGATGTTAA | 93664 |
rs368734507 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122399817 | TCAGCCTCCCGAGTA[C/G]CTGGGACTACAGGCG | 93664 |
rs368742639 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122886675 | CGGTTCCCCAGAGCC[A/C]GCCGGCAGAGGCGGA | 93664 |
rs368742944 | snp | C/T | 1.65625e-05 | 0.00287766 | missense | CADPS2 | GRCh38.p7 | 7:122393490 | TGTGAATTGACTGGG[C/T]GATGGAAGACTCCAT | 93664 |
rs368744018 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122807141 | CAGTGCATGCAGGGG[-/G]CATGTGCTGGTGGCC | 93664 |
rs368763416 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122597772 | TAACCAATCAAGTAA[C/T]GTATCTGATATGCTT | 93664 |
rs368781985 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122580075 | CCATTAATACCAGAC[-/T]AGAAATTTTCAAGTA | 93664 |
rs368782631 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122446808 | GGCTCTACCTAGGTT[C/T]CTCCTTTCTGGATCA | 93664 |
rs368785223 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122470375 | TGAATAAAAAGTTAA[C/T]GGGCCATTAATGGAG | 93664 |
rs368793188 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122422051 | TCCTGACGTTCAGGA[A/G]ATGGCTGAGGTGAGA | 93664 |
rs368800593 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122511814 | GAATGAAATATATCC[A/G]TAAGATATAAATGTG | 93664 |
rs368802907 | in-del | -/GAA | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122562491 | TAGAAAGGAACAGAA[-/GAA]CCCTGCTGAGAGCTT | 93664 |
rs368804195 | in-del | -/GTTAGT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122486924 | AAGTCTCAGGTGATT[-/GTTAGT]ATTTTTAGCAATAAA | 93664 |
rs368808446 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122522283 | CCATACCCAGCTAAT[A/T]TTTGTACTTTTGGTA | 93664 |
rs368809035 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122746763 | CTCTATCACTACATT[C/T]CCCTTACCCACTGTT | 93664 |
rs368822759 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122445623 | AGAATTTAAGAGTAG[C/T]CCTGGGCAACATAGG | 93664 |
rs368825669 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122837272 | TCTCTGGGACACATT[C/T]AAAGCAGTGGGTAGA | 93664 |
rs368829878 | snp | A/G | 8.30806e-05 | 0.00644464 | intron-variant | CADPS2 | GRCh38.p7 | 7:122438319 | TCTCACTGCCACTTC[A/G]ACAATTGCTCACTGC | 93664 |
rs368833999 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122411416 | GTAGAGATGGGGTTT[C/T]GCCATGTTCGCCAGG | 93664 |
rs368841515 | snp | C/T | | | upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122888276 | GACTCAAAACAGTTT[C/T]CTAGTTCCAAATAGT | 93664 |
rs368845403 | snp | C/G/T | 6.62706e-05 | 0.005756 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122702431 | AAAGTACAGCCTCCA[C/G/T]GTTCGATGAGGGCCA | 93664 |
rs368852857 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122369195 | GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACTGC | 93664 |
rs368856080 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122646454 | AACAAAAGTGAACAG[A/G]CACAGGGGCAGGAAG | 93664 |
rs368865755 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122334519 | GTAGGGATATAAGAG[C/T]TTGTTTGGGAGCTGA | 93664 |
rs368869240 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122572130 | AAAATTTAATGGCTA[A/C]TTTTATTGAAACAGC | 93664 |
rs368871112 | in-del | -/A | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122618282 | AAAAATCCTTAATCC[-/A]GTAAGTATTTATTGA | 93664 |
rs368883067 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122643434 | TCTGTCCTCAGCTGT[G/T]CTAGGCTTCAGAGTG | 93664 |
rs368892311 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122645408 | GTATATATGTACATA[C/T]ACACACATGTATATG | 93664 |
rs368897228 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122722630 | GCCCAAGGTAATTTA[C/T]AGATTCAATGCCATC | 93664 |
rs368899543 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122776681 | ATGTGGGAAAGTTTA[C/G]AATTTCCTAAAGACT | 93664 |
rs368903940 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122561475 | TTGTTATTTGCATGA[C/T]GGGAGGATTAAGGAT | 93664 |
rs368904950 | snp | A/G | 1.8448e-05 | 0.00303705 | intron-variant | CADPS2 | GRCh38.p7 | 7:122393172 | AGCTAACACACCACC[A/G]GGAAATAAGTGAGGA | 93664 |
rs368907972 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122415526 | TATTTATGGAATTAT[A/G]AGAGAAATAGAGTGA | 93664 |
rs368915676 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122581415 | AGCTTTTTATCTTTG[C/T]TTTTGTTTCTAGCAG | 93664 |
rs368923379 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122438190 | TGAATAGGAAAAAGC[A/T]CTTCAGTTCACCAGC | 93664 |
rs368934179 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122541099 | AAACAAAAATATGTG[C/T]ACCAAATAGGTGATA | 93664 |
rs368944991 | snp | A/G | 4.97863e-05 | 0.00498906 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122701960 | TCTTGGGGTTTGTAT[A/G]TGTCAAAGCAAACAA | 93664 |
rs368970399 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122380383 | ACAAAATGCATAGAG[G/T]AAAAGTACTCAGGTC | 93664 |
rs368977031 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122660085 | CATCAGAGGAGGAAT[A/C]AATGAAGGTAAAATA | 93664 |
rs368978993 | snp | A/T | | | intron-variant, upstream-variant-2KB | CADPS2, LOC105375481 | GRCh38.p7 | 7:122529470 | ACTAGGGATAAAGAC[A/T]AGAAATCTGTTACAT | 93664 |
rs368990088 | snp | G/T | 0.000155219 | 0.00880826 | intron-variant | CADPS2 | GRCh38.p7 | 7:122388787 | TCCCCGTTAATTAGG[G/T]ATACCATTAATACAT | 93664 |
rs369010555 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122591521 | CAAAAAAGAGCCTGC[A/T]TTGCCAAGACAATCC | 93664 |
rs369022148 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122871440 | CAAATACATGCATAT[A/G]TACATTTATATTTAT | 93664 |
rs369022234 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122344110 | AACACTGACACGAGA[C/G]ACCACGGCAGAGAGG | 93664 |
rs369023498 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122776566 | AGGGCTCAGAAAAAA[-/A]GAAAAAAAAAAACTA | 93664 |
rs369026252 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122815400 | CACATCTGGAAAAGC[C/T]GATAACAGCTAATTT | 93664 |
rs369027971 | snp | A/C | 2.44382e-05 | 0.0034955 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122491418 | AAAGGTATATTGGCT[A/C]ACCTGCTCGAGAAAA | 93664 |
rs369028561 | in-del | -/TTTCTTCACAGAA | 0.0193772 | 0.0965046 | intron-variant | CADPS2 | GRCh38.p7 | 7:122722665 | CAAGCTACCAATGAC[-/TTTCTTCACAGAA]TTGGAAAAAACTACT | 93664 |
rs369030471 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122575779 | TGCTGAGGCATTTCA[C/T]AAAATATTTAAAAGC | 93664 |
rs369031889 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122439193 | CAAGGGGAAAATGCA[A/G]TTACATCCAGAATTC | 93664 |
rs369032733 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122648637 | CCAGCAGGTAAACAC[C/T]GACAATCCCTAGATC | 93664 |
rs369055214 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122687257 | CTCCTTTTTCTTTCC[A/T]AATTATGTTGAGATC | 93664 |
rs369066868 | snp | G/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122538142 | CCCACTTATACAAAT[G/T]CAGTAAAAAAAAAAA | 93664 |
rs369072693 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122618709 | TAGGCTGAAATATGG[A/G]GTCTGAGGAGCAAGG | 93664 |
rs369077674 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122413178 | ATGGCTTTTTCAGCA[A/G]GCATCTGACACCTCC | 93664 |
rs369083990 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122353754 | AAATCTTCAGTACCA[C/T]ACCTGGCAAACAGTG | 93664 |
rs369086855 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122335455 | AGTTTCACCATGTTG[A/G]AAGTTCACATGTTGG | 93664 |
rs369089075 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122544394 | GCACAGTATCTAACC[C/T]TTGCTGTATAGCATA | 93664 |
rs369096443 | snp | A/G | | | downstream-variant-500B | CADPS2 | GRCh38.p7 | 7:122318397 | TTACACTTCAGGACA[A/G]AAGGGATGCATTATT | 93664 |
rs369098495 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122362395 | CCTTACTTCTCAGGC[C/T]TCCTCCATCAGTTAA | 93664 |
rs369103251 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122618992 | ACAATTTTATAAATA[C/T]GCAAACTTCTCAGAC | 93664 |
rs369124530 | snp | A/G/T | 3.29529e-05 | 0.00405901 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698585 | TAATTTTCTGTGTGA[A/G/T]GGTACAACCTCCCCG | 93664 |
rs369125924 | snp | A/G | | | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698320 | AAATATGCTAAGGTA[A/G]CAGTTGTGACAATCA | 93664 |
rs369135479 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122630249 | AGTTTACTTGTCACT[C/T]TCCCAAAGAACTACA | 93664 |
rs369136385 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122658217 | ACCAGTTAGAATGGC[A/G]ATCATTAAAAAGTCA | 93664 |
rs369140530 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122353033 | TTCAAAGCACATTCA[C/T]GTTAATGTGCTCATC | 93664 |
rs369141158 | in-del | -/GGGGTAACAAAGACCAGATCACACAGGACT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122626127 | AGATCACACAGGACT[lengthTooLong]TTGCAGGCCATTTTA | 93664 |
rs369141677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122650475 | TCTTATTTTTAAAAA[A/G]TGGAAAGTTGGGATA | 93664 |
rs369162837 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122327337 | ACAGTCAATTGAGGC[C/T]CTTCTACCACACCAC | 93664 |
rs369170034 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122721267 | CTGCTTGTTTGAAAA[C/G]ATCAACAAAATTGAT | 93664 |
rs369172887 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122498948 | ATCCTACAAAGCCTA[G/T]CTTAAGGGCTCACCT | 93664 |
rs369179326 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122705567 | TATTTATATTATATA[-/T]TATCTATATTATATA | 93664 |
rs369179605 | snp | A/G/T | 3.95275e-05 | 0.0044455 | intron-variant | CADPS2 | GRCh38.p7 | 7:122388759 | AGAAAAAGGAAAAAT[A/G/T]AACATCATGAACTCC | 93664 |
rs369191411 | snp | A/G | 0.140581 | 0.224783 | intron-variant | CADPS2 | GRCh38.p7 | 7:122645475 | TATGTGTATATATGT[A/G]TATATATTTAGCGTA | 93664 |
rs369200697 | snp | A/G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122754563 | CTCACTGCAACGTCC[A/G/T]CCTCCCAGGTTCAGT | 93664 |
rs369205831 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122500905 | GAACTGAAAACTAGT[A/C]AGGAAAAAGTGGTGT | 93664 |
rs369225521 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122409295 | GCAAAGAGACATTTT[C/T]AAAATCTCACTTCCA | 93664 |
rs369244978 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122874348 | GAAGGACCTCTTCAA[G/T]GAGAACTACAAACCA | 93664 |
rs369248727 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122709915 | ACTGTTGTGGGGTTG[C/G]GGGAGAGGGAAGGGA | 93664 |
rs369249992 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122609197 | GATACTTAACACTTG[A/G]AGGGAATAAAAGACT | 93664 |
rs369253740 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122826661 | TTAGAAATGCAGTAT[A/T]CAATAATCAAAATAA | 93664 |
rs369268544 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122430850 | TTTTATTCTGCAAAT[G/T]TGTGCTGCCAGTGGA | 93664 |
rs369285126 | snp | A/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122534904 | CTCTAAATTATTCAA[A/T]AGTAGTAATGGGGAG | 93664 |
rs369285395 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122408250 | ATTCTCAATGATAGC[A/G]TAGTAAATATTTTTA | 93664 |
rs369292726 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122489105 | AGTTTTCACTACATA[C/T]AAAAGATATGCCCCA | 93664 |
rs369298019 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122503903 | TTTGGGTGATGAATT[C/G]TTTTGCAGGAAAACA | 93664 |
rs369331950 | snp | C/T | 8.42922e-05 | 0.00649145 | missense | CADPS2 | GRCh38.p7 | 7:122360968 | AGAAAGTGCCTTCAT[C/T]ATACCTTGACAGCTT | 93664 |
rs369344568 | snp | A/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122541857 | TATATTCATATATAT[A/T]TATATATATGCATAT | 93664 |
rs369344819 | snp | A/C | 0.000165986 | 0.00910854 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122474402 | AGAATAGGAATCATT[A/C]AGTCTGTGATCCAAA | 93664 |
rs369345208 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122376088 | CCCAAAAGATAACAG[C/G]TATTAGTGAGAATGT | 93664 |
rs369347476 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122406174 | GTGATTTCCCCCCCA[C/T]CAGTTTTATCACAGA | 93664 |
rs369355149 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122692227 | TTGACTCCCGCAACA[C/T]AGCGGGGGTGCAGGC | 93664 |
rs369356977 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122597328 | TAACTATCATTATAT[C/G]TGGCAAATCAGAAGG | 93664 |
rs369357728 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122472704 | ATTGATGTTCACTCT[A/T]TGTGTTTGTCCATGA | 93664 |
rs369359467 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122357575 | AGTGTCATGTATCTA[C/T]CATTACAATATCATA | 93664 |
rs369367744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122331743 | GCATATCTGGAAACC[A/G]AGTTTACAGAGGCAC | 93664 |
rs369367968 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122853994 | TCCTTCAAAGAGCCT[A/G]CAGCAATTCGTTAAC | 93664 |
rs369371164 | in-del | -/TG | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122615399 | GAAGATTGACAAAAC[-/TG]AAAAAAAATTTGTTT | 93664 |
rs369372704 | snp | C/T | 1.76291e-05 | 0.00296888 | intron-variant | CADPS2 | GRCh38.p7 | 7:122737072 | TTGTTTGTTAAGCTA[C/T]AAGAAAAAGAGAAAA | 93664 |
rs369378490 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122369908 | TATAATGCAAATCTG[A/T]TTAATTCCCTACCCA | 93664 |
rs369393609 | in-del | -/T | 0.416055 | 0.186885 | intron-variant | CADPS2 | GRCh38.p7 | 7:122428472 | ATATATATATATATA[-/T]TTTTTTTTTTTTGAG | 93664 |
rs369396974 | snp | A/G | 0.158962 | 0.232835 | intron-variant | CADPS2 | GRCh38.p7 | 7:122665002 | TGGGGTCTCATTTAT[A/G]TGACTCAGGCTGGTC | 93664 |
rs369412508 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122689319 | CACAAGTGCCACCTT[C/G]GGCAGCTGTGGCTAT | 93664 |
rs369422269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122857776 | TGGGTTCGTGGTCTC[A/G]CTGACTTCAAGAATG | 93664 |
rs369426513 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122553898 | ATTCTGAGGAAGTCC[C/T]GGATTTTTGGCAATT | 93664 |
rs369428775 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122786888 | GACCCATCCTCCCAG[A/C]CCTAAGCATCTTCCC | 93664 |
rs369439812 | in-del | -/AG | 0.00874735 | 0.0655527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122856593 | GAAGTCTTGGCTCCC[-/AG]AGCTTGCTTCACAAG | 93664 |
rs369439856 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122600307 | TCTCTTTCTAAAGAT[-/C]CCACCAACTGTGGGA | 93664 |
rs369460980 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122688623 | CTGGCTCTCCCTTGC[A/C]TTCAGGGTCAGCAGC | 93664 |
rs369463911 | snp | C/G/T | 6.81691e-05 | 0.00583785 | missense | CADPS2 | GRCh38.p7 | 7:122360944 | CAGTGAATGACAGAA[C/G/T]GGATGAAAAGAAAGT | 93664 |
rs369466864 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122608480 | AGCTGCAATGTTCTT[C/T]CAATAGTTTGACAGA | 93664 |
rs369471685 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122860995 | TATTTGCTTTATCCA[A/G]TCATCCAATGATAGA | 93664 |
rs369486711 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122499695 | AAGAAGAAACTATGA[C/T]GATGGGGTTAGGGTA | 93664 |
rs369493135 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122335051 | TAATTGTGACATAGA[C/T]AGCCATCTCTATGGG | 93664 |
rs369502593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122419541 | CCCTTAAATTATGTA[C/T]TAATTTTTGTATGTA | 93664 |
rs369504121 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122369133 | ATTTTTGTTTCCCCC[C/G]CCCCCCCCCTTTTTT | 93664 |
rs369506226 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122771794 | AGCAATGCAGTAAGG[C/T]TAAAAAAGAGAAACT | 93664 |
rs369510012 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122609031 | ATCTCTACAAAAAAA[-/A]TGACAAAATTAAAAA | 93664 |
rs369511974 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122575550 | CAAGCGATTCTCCTG[C/T]CTCAGCCTCCCAAGT | 93664 |
rs369535003 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122749956 | CATTTGTTCACCTGT[A/G]AGGTTAAAAAAAAAA | 93664 |
rs369535079 | snp | C/T | | | intron-variant, upstream-variant-2KB | CADPS2, LOC105375481 | GRCh38.p7 | 7:122529072 | GCCATCTACTGGACA[C/T]ATACATATTATTACT | 93664 |
rs369554616 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122485360 | GTAAATTAAAGTTGC[C/T]ACTCCAGTGAACACA | 93664 |
rs369561450 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122753791 | CGCTTGCATGCTCTT[A/G]GGGACATACACACTT | 93664 |
rs369569096 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122556494 | TAAAAATTGGTATTG[C/T]ACCAAACTCTGAACT | 93664 |
rs369571087 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122445635 | TAGCCCTGGGCAACA[C/T]AGGGAGATCCCATCT | 93664 |
rs369576004 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122465886 | AAGCCAATTTTGTAC[A/G]TCAACATAGATCTAC | 93664 |
rs369584868 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122705919 | TAATATATTATATAA[C/T]ATAATATATAATATA | 93664 |
rs369585808 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122842031 | TTAGCAGCAGCTGAG[C/T]TGTTACCTCCTAGGC | 93664 |
rs369587111 | in-del | -/AG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122386057 | ATTCTGCAGACTAAC[-/AG]GGGAGAAACATTTCC | 93664 |
rs369588158 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122716937 | ATGTGAACATGACTT[G/T]TTCTACTAGAACACA | 93664 |
rs369591821 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122593045 | TTCCAACTTGAGATA[C/T]CTAAATTGAATTACA | 93664 |
rs369602341 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122323456 | CTAAAATATTCACTA[C/G]TGAGAATACTTAAGA | 93664 |
rs369604656 | snp | C/T | 1.64855e-05 | 0.00287097 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698318 | TGAAATATGCTAAGG[C/T]AGCAGTTGTGACAAT | 93664 |
rs369622273 | in-del | -/GTGTGT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122527618 | AGAGAGAGAGAGAGA[-/GTGTGT]GTGTGTGTGTGTGTG | 93664 |
rs369635789 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122566464 | AAGAGATATCTGCAC[-/T]CCAATGTTCATTGCA | 93664 |
rs369650567 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122629810 | AGTCTTCATATACTC[C/T]TCATTCTAATACCAG | 93664 |
rs369655649 | snp | C/T | 1.66532e-05 | 0.00288554 | intron-variant | CADPS2 | GRCh38.p7 | 7:122474344 | ATCTAAAATCTTTTA[C/T]TCCAACTTATAGGGG | 93664 |
rs369664900 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122519181 | CATTGTACATGACAT[C/T]TTCACAAGCACATAT | 93664 |
rs369672194 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122709625 | ATGTTTATTGCGGCA[C/T]TATTCACAATAGCAA | 93664 |
rs369676271 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122819092 | TTGCCTCCACTGTGA[A/G]ACAAACCCCAGCCAC | 93664 |
rs369676388 | in-del | -/AACTCAATTTC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122343747 | AATGGGAATAACATC[-/AACTCAATTTC]CCTCTTCTGTTCAAC | 93664 |
rs369681357 | snp | C/T | 0.000100469 | 0.00708691 | synonymous-codon, utr-variant-5-prime | CADPS2 | GRCh38.p7 | 7:122736988 | TGCGTTGCAAAATGC[C/T]TCGTCAGCTACAATT | 93664 |
rs369683873 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122612828 | TCCAGAAAGTGTGGT[A/G]GTGGCATAAGAATAG | 93664 |
rs369700799 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122497011 | ATATACCTGGGATTG[C/T]TACTTCTTTCTCGGA | 93664 |
rs369702188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122881526 | CAAGGTATTCCCTAT[A/G]ATTAAAAGCAGCAAA | 93664 |
rs369720354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122405535 | GGGTGTGGTGGTGCA[C/T]GCCTGTAATCCCAGC | 93664 |
rs369729215 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122717891 | CATAGGTCACTGCAG[A/C/G]CTTAACTAGCTGAGT | 93664 |
rs369730701 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122735380 | TGATCACTAAATTTG[C/T]GCACTTTTTTTATTC | 93664 |
rs369730927 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122457142 | AAATTTAGTTTCTAT[A/T]AAGGTAAAGAACAAC | 93664 |
rs369739482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122769781 | GTTTGAACCTACCAA[C/T]TGTTGACTGTGTAAC | 93664 |
rs369766667 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122503446 | AAACTAGTATCTACT[G/T]CAACTATTTAAACTC | 93664 |
rs369768951 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539783 | TCTCTCTCTTTCTGT[C/T]TCTCTCCATCTCTCT | 93664 |
rs369777214 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122461245 | ATAGAAGATAAAATG[C/T]CTAGTACATGGGTAA | 93664 |
rs369778350 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122495614 | CCATGATGGACATTC[C/T]TGTACGTCTTGTCTT | 93664 |
rs369786401 | in-del | -/ACTA | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554187 | GTCTATGGAAGTTTA[-/ACTA]TTTCTAGGAACCTCA | 93664 |
rs369798683 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122763304 | ATGAAACTAAGGGAT[A/T]CCTCCCCAGAAAGAA | 93664 |
rs369798781 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554882 | ATTTTTTTGACAAAT[A/G]TGTGTTTTCACATTA | 93664 |
rs369801255 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122853668 | GAGTCACAAATGAAT[A/G]TACATGTATGTAACT | 93664 |
rs369805228 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122443780 | TATTTAAACTTTATA[G/T]CCTTCAATTGTACAT | 93664 |
rs369824126 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122449016 | CAATGTGAGAATCAC[A/T]AAGAAAGAGAGCTGT | 93664 |
rs369833260 | snp | C/T | 6.71254e-05 | 0.00579294 | intron-variant | CADPS2 | GRCh38.p7 | 7:122407527 | ACATATGAAAGAAAA[C/T]GCAAATGCTCACTGT | 93664 |
rs369839045 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122650055 | CTGGGATTACATGCG[C/T]GTGCCACCACACCTG | 93664 |
rs369852993 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant, synonymous-codon | CADPS2, RNF133 | GRCh38.p7 | 7:122698079 | GGGGTCAATGCAATT[C/T]TTGTGGAAAAAATGT | 93664 |
rs369860621 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122525140 | GTGAGACCCTGTCTC[A/C]AAAAAAAAAAAATTC | 93664 |
rs369879996 | snp | G/T | | | utr-variant-3-prime | CADPS2 | GRCh38.p7 | 7:122319782 | ACTTCTCACAATGCT[G/T]CATTATGAGAAATAT | 93664 |
rs369880393 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122793849 | CTCCCTTAGCATTTG[C/T]CTTTCTGAAAAAGAT | 93664 |
rs369885775 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122605183 | AAAGGAAATTGCAGG[A/G]CGGGAAGTTGCTCTA | 93664 |
rs369887546 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122495350 | CTTTTCTGTTTATTA[C/T]ATTATTTCCATGACG | 93664 |
rs369889182 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122447943 | AAGGAACATTTTTTT[-/T]AGTGCATGTCTAAAA | 93664 |
rs369889267 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122845168 | CATAAAAGATCTGAA[A/G]TAATAAATACTTTTC | 93664 |
rs369889750 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122841620 | CAAGCTTTGCCGCAA[G/T]AGTAGGAGAAAACAC | 93664 |
rs369895784 | snp | G/T | 0.000167986 | 0.00916322 | missense, utr-variant-5-prime | CADPS2 | GRCh38.p7 | 7:122736956 | CTCTTCAAACTTACC[G/T]CATAATAACTCCGAA | 93664 |
rs369898767 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122834721 | ATCAAACTGCAAGGC[A/G]GCAGCGAGGCTGGGG | 93664 |
rs369910170 | snp | C/G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122511798 | TTGTCAAATTAGATA[C/G/T]GAATGAAATATATCC | 93664 |
rs369918462 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122829664 | CCAGCCATCAGCTTC[C/T]ATCATTTCATGTATT | 93664 |
rs369922773 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122526612 | ACCCCATTTGTCCCA[C/T]ACATTGTACAATTTC | 93664 |
rs369924862 | in-del | -/ACCCCAT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122696502 | CTTTAGTCTTCCATG[-/ACCCCAT]GGTCATGGAAGCAGT | 93664 |
rs369927226 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122366668 | ATACATACACACATA[C/T]ATATATATATATATA | 93664 |
rs369936048 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122871678 | CTGGGTCACCAATGT[A/T]AAGGGTAATCTCCAT | 93664 |
rs369956136 | snp | C/T | 0.000159987 | 0.00894248 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122702465 | ATGAGTCTGCCTGTT[C/T]GGGCCTGCTGAAATT | 93664 |
rs369958575 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122382760 | AGTTCAAGGTTGCAG[C/T]GAGCTATGAATATGC | 93664 |
rs369960316 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122635883 | CCTTCCTGATTGTTA[C/T]TGGTTTCAAATCTAT | 93664 |
rs369970175 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122634258 | TTCTTTGTACATCTG[G/T]TAGAATTCAGCTATA | 93664 |
rs369974553 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122819641 | CAGTACTCTTTTAAG[C/T]ACTCCTTTTTAGTTA | 93664 |
rs369989638 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122519092 | ATGGCCCTGGGTTGG[C/G]GCGGGGGAGGGAATC | 93664 |
rs369994717 | snp | A/G | 2.16237e-05 | 0.00328807 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122629268 | CCATTTTATCTGCCA[A/G]TTGCAGCCGGCCATC | 93664 |
rs369996084 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122431627 | TACTAGCTATGGGAC[C/T]GTAGACACACTACAT | 93664 |
rs370020075 | snp | A/G | 0.000147422 | 0.00858424 | intron-variant | CADPS2 | GRCh38.p7 | 7:122491272 | ATAAGAATTCCATGC[A/G]TACATACATGGCAGG | 93664 |
rs370021822 | snp | C/G | 0.000106022 | 0.0072801 | missense | CADPS2 | GRCh38.p7 | 7:122388635 | GTTTAAGTCTTTGCT[C/G]TAAGTGGTGGGCAAA | 93664 |
rs370023900 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122575112 | TATTCTGGATTTTTC[C/T]AATCCAGAATAAAGA | 93664 |
rs370028127 | in-del | -/AT | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122541817 | TATATTTATATATTC[-/AT]ATGTTTATATATTCA | 93664 |
rs370044781 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122334667 | CTCTAAACCTTTAGC[A/G]AGTTTACAGTCATCC | 93664 |
rs370059051 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122821828 | AAAAAGGACTGGACA[A/T]TACTTTTACCACTTT | 93664 |
rs370065567 | snp | A/G | 0.000253872 | 0.0112637 | intron-variant | CADPS2 | GRCh38.p7 | 7:122360832 | TCACCTTAAGTGTGA[A/G]AGAAAGAGATAATCA | 93664 |
rs370066287 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122425409 | CCTGGGCAACGTGGC[A/G]AAACCCTATCTCTAC | 93664 |
rs370068885 | in-del | -/GTCTCAATT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122469412 | TCTATTTTTTGATAT[-/GTCTCAATT]CCCCTAGTCAGAAGG | 93664 |
rs370075170 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122376197 | TGAAAAATAGAACTA[C/T]CATATGATTTAGCGA | 93664 |
rs370088115 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122682228 | CAACAAAGACTGAGA[C/G]CCTAAAGTGGAAGAA | 93664 |
rs370090192 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122865438 | GTGAGACCCTGACTG[C/T]TCCACAGCCAGCTAC | 93664 |
rs370093842 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122773690 | ATTGCTTTTTCAGGC[A/T]TTGCTTTAATCACAG | 93664 |
rs370097321 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122610816 | AAAATAATCTAAGGA[A/C]CATGAAAGAGCTTCC | 93664 |
rs370097607 | snp | C/T | | | utr-variant-3-prime | CADPS2 | GRCh38.p7 | 7:122318581 | TGGAGAAAATAGTAT[C/T]TGGTGTGTGAATAGA | 93664 |
rs370102836 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122639179 | TATGTAATGTTAGAA[C/T]TGAAGGGGATAAATT | 93664 |
rs370116680 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122724916 | AAAAATAAGTCCATA[C/T]GATTACAGAGAAAAG | 93664 |
rs370125415 | in-del | -/A | 0.493925 | 0.054776 | intron-variant | CADPS2 | GRCh38.p7 | 7:122705743 | TATATTATATAATAT[-/A]TAATATATATAATAT | 93664 |
rs370141461 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122514574 | TGGGAGTGTAACATC[G/T]TGGGAGATGATCTTC | 93664 |
rs370147382 | snp | C/G | 1.72779e-05 | 0.00293916 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122701852 | GTTTTCAGGATGTCA[C/G]ACTTGCACATGGGAC | 93664 |
rs370151044 | snp | A/C | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122562974 | CAAAGTTCAAGTTCC[A/C]CACAACCTAACGATT | 93664 |
rs370153339 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122542591 | TAGATATTGTGGAGG[A/G]TAACTTTATCTATAT | 93664 |
rs370156575 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122666363 | TTTTTTTTTTTTTTG[A/T]GATGGAGTCTTGCTC | 93664 |
rs370160688 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122581757 | TTTTTAAAGTAAGCA[C/T]AATTATCTCAGATCT | 93664 |
rs370163159 | in-del | -/TTTTTTT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122367540 | TAAACCTTCCCCCAG[-/TTTTTTT]TTTTTTTTTTTTTTT | 93664 |
rs370170873 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122837678 | AAACTAGAAAATCTA[C/G]AAGAAATGGATAAAT | 93664 |
rs370180972 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122487755 | ACATTACACAGGTAT[A/G]GATCTGGAGGCATTC | 93664 |
rs370185604 | snp | G/T | 4.98616e-05 | 0.00499283 | intron-variant | CADPS2 | GRCh38.p7 | 7:122325436 | TGCCATTATTCCTTA[G/T]AGCTTAGTGGGCAAT | 93664 |
rs370186551 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122659310 | AGGAAATGCTAGACA[A/T]AAAAAAAAAAAAAAA | 93664 |
rs370187543 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122645558 | TATATATATACTTAG[A/G]GAATATATATGCATA | 93664 |
rs370187989 | snp | A/G | 1.66852e-05 | 0.0028883 | missense | CADPS2 | GRCh38.p7 | 7:122438398 | AGGCAGCTTTCTCGA[A/G]ACATTTTCTGACCAC | 93664 |
rs370189157 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122587702 | GAATATATGTGTGCA[C/T]GTATCTTTGTAACAG | 93664 |
rs370192555 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122820021 | TCCCCCATTTTACCT[C/G]TCCTAAAACCAGACA | 93664 |
rs370204079 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122385732 | TCTGATGATGGTCAC[A/C]TCCTAGGCCATGAGT | 93664 |
rs370207701 | in-del | -/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122538593 | ATATTGATAGTTCAA[-/G]GAGAAAAATATCATT | 93664 |
rs370209216 | snp | C/G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122469547 | GGGTTGAGTGTGAGA[C/G/T]AGTGGGGAAAAAACT | 93664 |
rs370211791 | snp | C/G/T | 0.000328779 | 0.0128178 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122702651 | TCCAAATGGCTTTTC[C/G/T]GTTTGAGTCAGGAAA | 93664 |
rs370224462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122352627 | GTGCATCCCTCTCTC[C/T]AGGTGAATATGCCCC | 93664 |
rs370226489 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122320497 | GTATTTCTGGGGAGT[A/T]AATGGAATGACAGAC | 93664 |
rs370234391 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122658893 | TATAATAAAAAAATT[A/C]AAAATAAGGAGATTT | 93664 |
rs370238800 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2, RNF148 | GRCh38.p7 | 7:122701214 | GGCAAAAAGGGATAC[A/G]ATTAAGAAAATGTGG | 93664 |
rs370243605 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122804643 | TTATCTTATGAATGG[C/T]AATTATACTCAATAT | 93664 |
rs370252936 | snp | C/G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122420683 | TGGCTCTACATCCTT[C/G/T]AAGCTTCACACCAAA | 93664 |
rs370259678 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122446406 | CCTATTTGAATCTTG[A/T]TTTTAATCCCCATTA | 93664 |
rs370297573 | in-del | -/CTC | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122350445 | TATTTGAATAAAAAT[-/CTC]CTGAAATTTTTCAAA | 93664 |
rs370298247 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122724877 | GATTGTGATCTCTTC[A/T]CAGGATTATGCTTTT | 93664 |
rs370306205 | in-del | -/A | 0.00485759 | 0.0490428 | intron-variant | CADPS2 | GRCh38.p7 | 7:122393175 | TAACACACCACCAGG[-/A]AATAAGTGAGGAATA | 93664 |
rs370306243 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122605475 | TAGCAATATGATCCC[A/C]CCACCGATGAAAAAT | 93664 |
rs370311745 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122838457 | GAGGAAGAAAGAAAG[C/G]GTACTCAATTAGGAA | 93664 |
rs370314521 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122781605 | AATATGCAACACTCA[C/T]AAATAATGTATCCTT | 93664 |
rs370320143 | snp | C/G | 1.71725e-05 | 0.00293018 | missense, intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554635 | TATTTTTTGGAACTA[C/G]CATTCGGTGTAATTC | 93664 |
rs370321008 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122631013 | TAAAATCAAAATGAT[G/T]AAAATTAAAAACTAA | 93664 |
rs370333922 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122760558 | TCAGTACCATCCCTA[C/G]TTAATACCAAAGAAT | 93664 |
rs370340465 | snp | C/T | 3.31719e-05 | 0.00407245 | missense, utr-variant-5-prime | CADPS2 | GRCh38.p7 | 7:122621507 | ATGACAGTACCACGT[C/T]GGACTTTGACAGCTG | 93664 |
rs370364586 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122497959 | CTGCAGTTCTCCTCT[C/T]GTAATTTGCTTTTTT | 93664 |
rs370385052 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122852266 | ATCTAGGAACTCATT[C/T]AATGGTACCTGAATT | 93664 |
rs370386849 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122746552 | CTTCCCTGGGCCATA[C/T]TGGAAGAAGCAGATT | 93664 |
rs370389120 | in-del | -/TAAA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122647795 | GCTAATCAGAACAAA[-/TAAA]CAATTAAAAACAAAG | 93664 |
rs370391043 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122771522 | CATATGATTTTTCCT[C/T]TCAAGAAATTTCCAG | 93664 |
rs370397056 | in-del | -/AA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122393077 | AAATAAAAAAAAAAA[-/AA]CAGTATTCCTCAACC | 93664 |
rs370402886 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122679007 | GTTGCCCAGGACCCT[A/G]TAATGACTGCGTTAA | 93664 |
rs370404963 | snp | C/T | 7.18107e-05 | 0.00599168 | intron-variant | CADPS2 | GRCh38.p7 | 7:122361035 | TACAGTTATAGTGAG[C/T]ATTTAGAATGTTACT | 93664 |
rs370413712 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122693261 | AATATCATTTCCTTC[C/T]TTAAGTGTTCCCTAA | 93664 |
rs370426775 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122722432 | AATCATGAGTGAACT[C/G]CCATTCACAATTGCT | 93664 |
rs370430049 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122329051 | ACTTGTGCATTTTTA[A/G]TAACAAGAGGGTCAA | 93664 |
rs370433409 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539740 | CTCTGCCTGTCTGTC[C/T]CTCTCTCTCTGTCTC | 93664 |
rs370434103 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122601274 | AAATGCTGCCATCTG[C/T]CAGCAAAGCTATATT | 93664 |
rs370444669 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122774140 | TTCAATTTCAATCAC[C/T]ATTGCCATATATATT | 93664 |
rs370446962 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122877172 | AACAAAACTAGGCAT[C/T]CACCTCTATTAATAC | 93664 |
rs370447154 | snp | C/T | | | intron-variant, upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122622224 | TAAAAACTCACATTA[C/T]TGAAGAGTGATATGG | 93664 |
rs370449308 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122667514 | CATTTAGTGTCAACA[A/G]CATTTCAGGGATTCT | 93664 |
rs370457641 | in-del | AA/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122794752 | GAACTGAAATCATTT[AA/T]AAAAAAAAAAAAAAA | 93664 |
rs370463218 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122775415 | GGTGATTCAAGGTAG[C/T]CCAGGGGGATGCTGC | 93664 |
rs370474828 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122565616 | CTTGACTCATACAAC[A/C/G]CATATAATACAAACC | 93664 |
rs370480151 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122491013 | TTCTGCTATAACTTT[C/T]GCTTTCCCGCAAAGA | 93664 |
rs370481175 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122740751 | AACTAGAAAAAAAAA[-/A]TACTTGCAACTCATT | 93664 |
rs370481286 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122642542 | CTACTAAGTTTCACC[C/T]AACAGCTTTTTTTTT | 93664 |
rs370489771 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122361965 | GTAATCTTAGCTACT[C/T]GGGAGGCTGAGGCAG | 93664 |
rs370495489 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122875956 | CCCTAAGGGAAACAC[A/G]AAGAAAGGATACAAA | 93664 |
rs370520696 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122415747 | TTCCCCCTTCTTCAA[C/T]AACTGATGAGCTAAT | 93664 |
rs370525070 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122767637 | GCCTTTCTCTCACTC[C/T]CCGGGACCTACCCAT | 93664 |
rs370527418 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122738893 | CCATGGGCAGCGAAG[A/C]AAGAAGACCATTCCA | 93664 |
rs370544274 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122363516 | TGAGGGACAAAGCAA[A/G]ATAGAGGCAGGGAGC | 93664 |
rs370563302 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122833541 | GCTTTGTTTTTTTTT[-/T]GTTTGTTTGTTTTGT | 93664 |
rs370565841 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122637046 | TTATTTTTTTAAATT[A/G]TTTATTTATTTTTTT | 93664 |
rs370571468 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122610220 | AAGTATTTTAGTTCA[C/T]TTATATTGTTCATGC | 93664 |
rs370574330 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122354840 | TGGGGCCATAAACTG[C/T]ATAACTGCCACAGAA | 93664 |
rs370579547 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122830555 | CATATATAGCGCATT[A/G]GCAAAGGATAATGAA | 93664 |
rs370583138 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122507992 | CTAAATTAAAAGGGG[A/C]ATATTCATTTATATA | 93664 |
rs370593727 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122778812 | GGGACTGTTGGGAAG[A/G]CATGATTAGTTTTAA | 93664 |
rs370602630 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122547059 | GATAATATGAACGAA[A/G]CTCAAATCTAGGGTG | 93664 |
rs370616836 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122494697 | GAATAAAGTTATTTC[G/T]ATTTTGAAGAATAAA | 93664 |
rs370621755 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122626017 | CAGGGCCAAGACCCT[A/G]TGGCAAGGAAAGGCA | 93664 |
rs370627372 | snp | C/G | 1.71108e-05 | 0.00292491 | intron-variant | CADPS2 | GRCh38.p7 | 7:122621447 | GCATCATCATTTATG[C/G]TGTCAGAGGTGAGCA | 93664 |
rs370629007 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122855391 | AAAAATGTGGTTATT[A/G]TCATACTTCTAATAA | 93664 |
rs370629341 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122522471 | TGTTTATGGGATACA[G/T]GTGACATTTTGATAC | 93664 |
rs370637070 | snp | G/T | | | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122699868 | GTTTGGCACAATTCA[G/T]TTTTTAAAAAACAGC | 93664 |
rs370643719 | snp | C/T | 5.14152e-05 | 0.00507001 | intron-variant | CADPS2 | GRCh38.p7 | 7:122320369 | AAAATTTGCTTAGCT[C/T]ACTTAGATTATATGC | 93664 |
rs370645255 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122345048 | ATTCAGAAGGCACCC[C/T]GCCATCCCCCCGGCC | 93664 |
rs370650170 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122582423 | AACTGGCATCTAGAT[C/G]CAGTCTTTTTTTTTG | 93664 |
rs370653073 | snp | C/T | 0.000167986 | 0.00916323 | missense | CADPS2 | GRCh38.p7 | 7:122615263 | CAATTCGATTGGGAG[C/T]AACTGACTTCAGGCC | 93664 |
rs370654451 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122852419 | TGAATGTGTTGTATA[A/G]TATATTAAGAGGTAA | 93664 |
rs370654967 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122658433 | TGCTATAAAGATACA[A/G]GCACAGTATGTTTAT | 93664 |
rs370665581 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122371012 | GACAGGTTAAGTGTA[C/G]GAACACTGCACTCTC | 93664 |
rs370666906 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122410746 | TGACTACCGCAATCA[A/G]TAATTACAAATATGT | 93664 |
rs370668131 | snp | C/T | 0.000875616 | 0.0209055 | intron-variant | CADPS2 | GRCh38.p7 | 7:122480054 | GGAGAGAACAAAGTA[C/T]AGTTTAACCAAAGAA | 93664 |
rs370668325 | snp | C/T | 6.64975e-05 | 0.00576579 | missense | CADPS2 | GRCh38.p7 | 7:122379409 | CTTTTACACTGTTGT[C/T]GATCAGATCATCTAT | 93664 |
rs370693639 | snp | A/G | | | intron-variant, upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122621794 | AATTGTATGATATAT[A/G]TACTTCACTGTCTTA | 93664 |
rs370698529 | snp | A/C | 8.26344e-05 | 0.00642731 | missense | CADPS2 | GRCh38.p7 | 7:122407624 | CCTCTAGTGCAGTGT[A/C]CATATCCACTGTAAA | 93664 |
rs370717469 | in-del | -/TTTA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122514358 | CATTATGATTATTTA[-/TTTA]GGGGCTTAAGATTTT | 93664 |
rs370719565 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122757193 | TCTTTATTGCCCAGG[A/C]TGGAATGCAGTGGCA | 93664 |
rs370719855 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122652269 | TATATATATATGCTC[C/T]GCATGATTATAGATA | 93664 |
rs370725203 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122422616 | CAGAAAATACTCTAT[C/T]TTAGGTAACTCATCA | 93664 |
rs370735514 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122731829 | CTTCCTATTCTGGTC[C/T]GTCCCTCTACCATCA | 93664 |
rs370739196 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122664295 | GGGCTAGAATATACC[G/T]GTCCCCATCCCTGAT | 93664 |
rs370744214 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122710545 | GGGCCTTGATGAGTA[C/T]TGGATGACATATTTC | 93664 |
rs370745967 | in-del | -/TCGAG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122708550 | TATATATATATATAT[-/TCGAG]ATATATATATATATA | 93664 |
rs370747989 | in-del | A/TT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122578657 | TAATGAGGAGTCTGA[A/TT]TTTATTCCAAATAAA | 93664 |
rs370764018 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122481215 | CTGTTGCCCAGGCTG[C/G]AGTGCAGTGGTGCGA | 93664 |
rs370769353 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122681046 | AAAAAACCAAACACC[G/T]CATATTCTCACTCAT | 93664 |
rs370779825 | snp | C/T | 1.90369e-05 | 0.00308514 | intron-variant, utr-variant-5-prime | CADPS2, RNF133 | GRCh38.p7 | 7:122698955 | TAAGAACCAACCTAA[C/T]AGTTGCACATCTGTT | 93664 |
rs370785130 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122433641 | CTCCTGACCTCAAGT[A/G]ATCCACCCATTTTGG | 93664 |
rs370785550 | snp | C/T | 8.28397e-05 | 0.00643529 | missense | CADPS2 | GRCh38.p7 | 7:122393535 | GGACAACCAAGGGTA[C/T]AAAGATTTCTTGCAA | 93664 |
rs370789406 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122718569 | ATGGCATATTCAGTA[C/T]CCACAGGTTTTTCTC | 93664 |
rs370794040 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122617169 | TGACCTCCTAAAACA[C/T]ACAACTTGTGAAACA | 93664 |
rs370799953 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122661577 | TCTCAGAACTGAAAG[A/G]AATTATAGCTTTAAC | 93664 |
rs370800653 | snp | A/G | 6.77794e-05 | 0.00582109 | missense | CADPS2 | GRCh38.p7 | 7:122438436 | ACCTCTTCTGCTGGT[A/G]TGGGAGTGGCAATAT | 93664 |
rs370806796 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122440112 | ATCAGTAAGTAAAGA[A/G]AAATAAAAATGAAGA | 93664 |
rs370807562 | in-del | -/TT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122471232 | TTGATGCACACTTTT[-/TT]CTCTGTCGTTTTTTT | 93664 |
rs370826241 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122337835 | TATAGAAACAGGCTT[-/A]GACTATGACTATCTT | 93664 |
rs370844646 | snp | C/G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122835450 | AATGACTTTGACGAG[C/G/T]TGAGAGAAGAAGGCT | 93664 |
rs370849267 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122593175 | ATTTAAGACATCAAA[A/C]TATACTACTCTATAT | 93664 |
rs370850752 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122794591 | AGATATTCAGGACCT[A/G]AGCTCAGTACTGGAT | 93664 |
rs370853340 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122884569 | TTACCTGAAGGATCT[A/G]TTATTAATCTCCAGC | 93664 |
rs370857475 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122857784 | TGGTCTCGCTGACTT[C/T]AAGAATGAAGCCGCT | 93664 |
rs370866893 | in-del | -/C | | | frameshift-variant | CADPS2 | GRCh38.p7 | 7:122393502 | GGGCGATGGAAGACT[-/C]CATGAGATCCACATA | 93664 |
rs370877468 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122883245 | ACTCACCAGCTCTAA[C/T]AGTGAACGGGCTTTG | 93664 |
rs370883806 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122572890 | GGTTGGCCATCAATT[C/T]GGATGAAAAATCTCC | 93664 |
rs370887928 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122582844 | TAATAGGTTTCCATA[A/G]AATTTGCTTTTTAAA | 93664 |
rs370904681 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122884466 | TGTGCCAATTTGTTT[G/T]GGATTGGGAAATGCT | 93664 |
rs370904877 | snp | C/T | 1.65748e-05 | 0.00287874 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122702140 | CAATCTAAGTAAAAG[C/T]AGGCAATTGTGGCAG | 93664 |
rs370908711 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122403539 | GTCAATGTATAGAAA[C/T]AGTTAAATCAGGAGA | 93664 |
rs370930913 | snp | A/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122533305 | CTTGATAACGACAAA[A/T]CTCTTTAACAATTAA | 93664 |
rs370939696 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122582923 | TTTCAAAATCCTTTG[A/C]AACTATTTACACTAC | 93664 |
rs370940998 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122827662 | AATGAAAAGAAAAAA[G/T]AATTAGCTACAATTC | 93664 |
rs370948214 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122589927 | GTTTACATGCAGTAA[A/C]ATGTAATCATCTCAA | 93664 |
rs370959860 | in-del | -/AAA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122581814 | CTGCCAAAAAGAAAG[-/AAA]TATGCATCATAAGAA | 93664 |
rs370976128 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122333888 | ATTTATAAATATAAA[A/T]TTATATATATATATA | 93664 |
rs370978478 | in-del | -/T/TT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122729676 | GCCCATTTTTAACGG[-/T/TT]TTTTTTTTTTTTTTT | 93664 |
rs370998344 | snp | C/T | 9.89985e-05 | 0.00703487 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698702 | GTGGCACTATAACTC[C/T]TGCCACTCTCTTCAA | 93664 |
rs371015369 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122579475 | TATATATATATATAT[A/G]TATATGTCACTTATG | 93664 |
rs371017970 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122532111 | ATCTAGGCTATGCCC[C/T]GACATTGCAAAAAGT | 93664 |
rs371042841 | snp | C/T | 0.295854 | 0.245759 | intron-variant | CADPS2 | GRCh38.p7 | 7:122822607 | TGACTTGCACGTATA[C/T]GCCCAGATGGCCTGA | 93664 |
rs371052408 | in-del | -/AAGAA | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122472357 | ATAAAGGAAAGGAGG[-/AAGAA]AAGAAAAGAAAAGGA | 93664 |
rs371056968 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122606951 | GAGGTCCCTGGCAGT[A/G]GGAGAACTGCTAAGA | 93664 |
rs371059134 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122689945 | TTTGTGACGCCTCCT[A/C/G]TTCAAAGCTTGATGT | 93664 |
rs371061620 | snp | A/C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122640007 | TTATGTGAAGACAAG[A/C/G]CACATTGAAATTAAC | 93664 |
rs371064793 | snp | A/G | | | intron-variant, nc-transcript-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122531130 | TCCATCAGTGACAGC[A/G]AGCTGTACTGGTAGT | 93664 |
rs371073552 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122513843 | ATTTGCTGATTTCTA[A/C]GGTCTCTGCTAGCTC | 93664 |
rs371086478 | snp | C/T | | | intron-variant, nc-transcript-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122531049 | GAAGCCTCACTGAGG[C/T]GCCATTTAAAGTCAG | 93664 |
rs371106932 | in-del | AA/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122337835 | ATATAGAAACAGGCT[AA/T]GACTATGACTATCTT | 93664 |
rs371108978 | snp | C/T | | | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122700617 | AGGTGTTTATTCATC[C/T]ACTAGAAAAAAGGAA | 93664 |
rs371112653 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122427541 | GAGTTCATCTGTATA[C/T]ATTAAATAAGCCCAT | 93664 |
rs371127285 | snp | A/G | 6.65724e-05 | 0.00576903 | intron-variant, missense | CADPS2 | GRCh38.p7 | 7:122393223 | AAAGAAGGCATCCAC[A/G]AAGCAGTAGAAATGT | 93664 |
rs371133946 | snp | C/T | 0.000169986 | 0.00921758 | missense | CADPS2 | GRCh38.p7 | 7:122513292 | CATCTTTTCCAAACC[C/T]TCTGTCCAAGGGCAT | 93664 |
rs371142744 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122776567 | GGGCTCAGAAAAAAG[-/A]AAAAAAAAAAACTAA | 93664 |
rs371167381 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122505724 | GCAATCTGGCGTTTC[A/G]AATACATCAACTCCA | 93664 |
rs371183610 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122743621 | TTTACCTCATGTCAA[A/T]GAGTAATAAAAATGA | 93664 |
rs371184149 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122627305 | GTCAATTGTTATTAG[G/T]CTTAAAAATATTTCA | 93664 |
rs371189474 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122731465 | AACAGAAGCAGATAT[C/G]TGAGGGGAAGAATAG | 93664 |
rs371190154 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122408816 | TTCTTAAGAACTTTC[A/C]ATGTTTATAAAAATT | 93664 |
rs371198783 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122354304 | ATAAGCCTATAAGAG[A/G]TGTAATTACATCTCC | 93664 |
rs371200552 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122662587 | CACCATGTTGCCCAC[A/G]ATGGTCTCAATCTCC | 93664 |
rs371201731 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122368724 | GTTTGAAAAGTCCCT[A/C]GTAGATGACCTCAGG | 93664 |
rs371204184 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | CADPS2 | GRCh38.p7 | 7:122607902 | TTGTGTGGTTTGAGT[A/G]TTTTGCCTTTGGTTC | 93664 |
rs371207080 | snp | A/G | 2.3193e-05 | 0.00340528 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122325570 | GACTTTCATGGAACT[A/G]CTGTACCATTGCTAG | 93664 |
rs371219858 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122644105 | AGGAATGAAGGAAGG[A/G]AGGAAGGAAGGAACA | 93664 |
rs371219887 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122766490 | GTTCACTCCCCACAC[A/G/T]CAAACCTGTTACCCA | 93664 |
rs371223748 | snp | C/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539729 | AAATCTTATAACTCT[C/G]CCTGTCTGTCCCTCT | 93664 |
rs371224130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122506899 | GAGAAAGAAAAGTCA[A/G]TCTTTTCAGAACAAT | 93664 |
rs371225546 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122764688 | AAAGGATGTAAGACT[A/G]GAGACCTAAGTGAAA | 93664 |
rs371225828 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122631548 | CCTTCCTAAGTGCTG[C/G]AATTACAGGCATAAG | 93664 |
rs371233725 | snp | A/G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122588134 | TCGAATGGATGGATT[A/G/T]CAACGATTTTCTCCC | 93664 |
rs371235834 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122683238 | ATCTGTAGTTTCTGA[G/T]GCTCAGTTGCTGCTT | 93664 |
rs371242602 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122586644 | GACATTTTCATCTTA[C/T]TTCTATTCAACAAAA | 93664 |
rs371246134 | in-del | -/T | 0.5 | 0 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122549630 | TAATTAATACTAATC[-/T]TTTTTTTTTTAAGAC | 93664 |
rs371266885 | in-del | -/AAAT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122884620 | GGATTCCCAGAGAAT[-/AAAT]GATTCCAAAATAGTT | 93664 |
rs371274680 | snp | C/G/T | 4.50879e-05 | 0.00474788 | intron-variant | CADPS2 | GRCh38.p7 | 7:122736905 | ATAAAAATAATAAAA[C/G/T]TCCTTTTAAAATGCA | 93664 |
rs371276214 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122705957 | TATAATATATAATAT[-/A]ATATATAATATAATA | 93664 |
rs371279926 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122389926 | ATTGTTTAAAGCACC[A/G]CATTGTTTCGCTAAA | 93664 |
rs371286808 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122475714 | ACATAATTCAAGCTG[A/G]AGGGTCTTCAGAATC | 93664 |
rs371294412 | snp | A/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122552794 | TTTTTTTTTTTTTTT[A/T]TTATTGTGCCATTCA | 93664 |
rs371304932 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122427975 | TCTTCATAGAGGTCT[A/G]TAAAGTTTCGCATGT | 93664 |
rs371325777 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122385617 | TTACGCATAAAGGTT[A/T]TCTAACCTTGTACCT | 93664 |
rs371362226 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122761668 | ATGAAGCACTAAAAA[C/T]GTATTAAGCAAACAA | 93664 |
rs371380344 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122660153 | AAAAGATAACTGTTC[A/G]AAGCAATAATAGAAA | 93664 |
rs371382537 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122813227 | GCAAGAAGTAAGTCA[A/T]TACCTACATTTTACA | 93664 |
rs371386193 | snp | C/T | 0.000799535 | 0.0199782 | intron-variant | CADPS2 | GRCh38.p7 | 7:122491277 | AATTCCATGCATACA[C/T]ACATGGCAGGAAAAG | 93664 |
rs371390195 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122790391 | GGGACAGCCAGACAG[C/T]GTTTCTAAAAAAAAA | 93664 |
rs371390372 | snp | A/T | 1.65696e-05 | 0.00287828 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122702434 | GTACAGCCTCCACGT[A/T]CGATGAGGGCCAGCC | 93664 |
rs371392647 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122847608 | TTAGATTTTTTTTTT[-/T]CTTGTCATCATTAAC | 93664 |
rs371400150 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122321968 | TCATTCTAAGTCATA[A/G]GTTATTATGACTAAG | 93664 |
rs371403948 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122709172 | CAAAAGGTTCTGCAG[C/G]CTGCTTCTGGGACTC | 93664 |
rs371424866 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122661306 | TACTTGCAATTCAGA[C/T]CTCCAACTGTAGCAG | 93664 |
rs371441389 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122705646 | TGATATATAATATAT[G/T]ATATAATATATCTCA | 93664 |
rs371443642 | snp | C/T | 1.66112e-05 | 0.00288189 | missense | CADPS2 | GRCh38.p7 | 7:122490110 | GCATGGAGAGTTCCT[C/T]CTTTAGGATTCAGTT | 93664 |
rs371445644 | snp | A/G | | | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122703325 | TCAACACTACCCAAT[A/G]TGGCATTCTGTGGGA | 93664 |
rs371446904 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122484739 | AGGAGAAAATATTTG[C/T]AAATCACGTATCTGA | 93664 |
rs371448225 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122614900 | GATAAAATTTGCTTT[C/T]CTTAGAAATGACTTA | 93664 |
rs371452728 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122583677 | AGATATTGTACGTGT[C/G]TATATACGTATATAC | 93664 |
rs371466744 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122645461 | CACACATATGTATAT[A/G]TGTGTATATATGTAT | 93664 |
rs371477561 | in-del | -/AG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122645527 | ACTTATATATATATA[-/AG]TATATATATATACTT | 93664 |
rs371489710 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122733370 | CAAGTATTCATTGAA[C/T]ATATTTGTGTGCTAA | 93664 |
rs371501286 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122411098 | TCATCTCTCTCTCTC[C/T]CCATCCATCCATCCA | 93664 |
rs371501905 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122678845 | GAAGTCAGGGACCTC[A/G]AATGGAGGGACCAGC | 93664 |
rs371532428 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122354262 | ATTCCATTCTAGGAA[A/C]TGTGAAAACTGCTTA | 93664 |
rs371540289 | in-del | -/AAG | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122501420 | CCAAGCTTCACTGAA[-/AAG]AAAATGAAATATTAT | 93664 |
rs371542669 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122558102 | TTTGAATTATTGAAA[C/T]GTAACGACTTTCTTG | 93664 |
rs371545177 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122785038 | TATTTTCATATTTAT[A/G]CTCTGGGATTTGAGA | 93664 |
rs371548339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122580930 | GCACATGTGTGAGAA[C/T]GACTGAGTTGGTGAC | 93664 |
rs371559545 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122612477 | AATAATAGAAATACA[C/T]GTAACAAAAAAATAA | 93664 |
rs371565965 | in-del | -/ATA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122705979 | AATATAATATAATAT[-/ATA]ATATTATATATTATA | 93664 |
rs371571057 | snp | A/C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122653616 | TGGTTTTTTTACACA[A/C/T]TGAAGGTCTGTGGCA | 93664 |
rs371576535 | snp | G/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122547759 | GAAGCCAGTTAAAAG[G/T]AGAATTGGAAGCAGA | 93664 |
rs371580885 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122540506 | GGAACTAAATTTATA[A/T]CTCGGCTCTTACAAA | 93664 |
rs371593653 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122429882 | CACAAACTGTGCAGT[G/T]TTTTTTTTTAATAAA | 93664 |
rs371601471 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122668545 | TAAAAAATATGGATT[C/T]ACTAGCAGTCAAGAG | 93664 |
rs371627647 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122619415 | CTCAGGAGTTTGAGA[C/T]CAACCTGGACAACAT | 93664 |
rs371634006 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122565173 | AAGCCCAGACTTCAC[C/T]GCTATGCAGTATAAC | 93664 |
rs371639699 | in-del | -/GA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122441073 | GAAATTCTGAGATGA[-/GA]ATATTGAATGAATGA | 93664 |
rs371655819 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554942 | TTCATAACGAATTAA[C/T]AGCACAACAAGCCAC | 93664 |
rs371660738 | snp | A/T | 0.159622 | 0.233092 | intron-variant | CADPS2 | GRCh38.p7 | 7:122705905 | TATAATATAATATAT[A/T]ATATATTATATAATA | 93664 |
rs371673169 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122747772 | GCTTGAAGAGGTAAA[A/C]GCTCCTCTCCTCCCC | 93664 |
rs371685730 | snp | C/T | 1.65132e-05 | 0.00287339 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698003 | CAACAACCACTTGAA[C/T]CCCCAAAACTTTAAG | 93664 |
rs371686773 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122418643 | GTAGGAATAGAAAAG[A/G]AGGGAAAGATGCACA | 93664 |
rs371698040 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122679872 | AATCTTGTGGCCTTT[C/G]ATTAGTTTTACAAAG | 93664 |
rs371701022 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122758171 | ACATGTATTACCATC[C/T]CATGCCCATGAAATT | 93664 |
rs371702734 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122705874 | ATACATATTATATAT[A/T]ATATAATATAATAAA | 93664 |
rs371706166 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122593818 | AAGCCATGTGAGAAT[C/G]TGAGGAGAGGAAGAG | 93664 |
rs371728806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122416987 | AAGATAAATGTTGTC[A/G]GGGATTCATAGGCTC | 93664 |
rs371743806 | snp | A/C | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122548021 | TACAAAATAAAAGTC[A/C]TGTAGACAGTAAGTA | 93664 |
rs371749186 | snp | A/C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122423924 | AACAAAGGTGACCTA[A/C/T]GTAAACTTTGATTAT | 93664 |
rs371752139 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122469373 | CATCCTCTTGCATTT[C/T]AGAGGTCTGCCTAGT | 93664 |
rs371753070 | snp | A/G | 9.27687e-05 | 0.00680997 | intron-variant | CADPS2 | GRCh38.p7 | 7:122386991 | ATGCCAAGGCACCCT[A/G]TGCTGCCTTTCCCCA | 93664 |
rs371765172 | in-del | -/AGAG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122527583 | AAGATAATACTGAAT[-/AGAG]AGAGAGAGAGAGAGA | 93664 |
rs371766524 | snp | A/G | 0.000179984 | 0.00948469 | intron-variant | CADPS2 | GRCh38.p7 | 7:122480908 | ATATTTAAATGGGTT[A/G]GGAACTATATACTTA | 93664 |
rs371766757 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122482879 | CAAGAATTCAGCTGA[C/T]TACCCATCAGCTCAT | 93664 |
rs371769432 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122397357 | TTGAAAATTTTAGAA[A/G]ATTGGCAGTATTATT | 93664 |
rs371770285 | snp | C/T | 1.66219e-05 | 0.00288283 | intron-variant | CADPS2 | GRCh38.p7 | 7:122438312 | TGTTGGCTCTCACTG[C/T]CACTTCGACAATTGC | 93664 |
rs371775244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122422953 | GACAGAGTGAGACTC[C/T]GTCTCAAAATAAATA | 93664 |
rs371778725 | snp | A/T | 0.158962 | 0.232835 | intron-variant | CADPS2 | GRCh38.p7 | 7:122665003 | GGGGTCTCATTTATA[A/T]GACTCAGGCTGGTCT | 93664 |
rs371784535 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122334601 | GTGCTCTTATCTCAC[A/G]GTCACGTCATTTGAT | 93664 |
rs371784594 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122705935 | ATAATATATAATATA[A/T]TATATAATATAATAT | 93664 |
rs371802142 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122783433 | TTTTCCTGCCGCAGC[A/G]TTCCTCACATGGGGC | 93664 |
rs371814285 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122343921 | AGCTGGATGGATGAT[A/C]ATTTTTCTACCCCTG | 93664 |
rs371818314 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122822723 | CGATCCTTGCCTTAA[C/G]TGATGACATTACCTT | 93664 |
rs371818527 | in-del | -/CCA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122674454 | TCAATCTGAGCACCA[-/CCA]ACTGCCACTCTTCCC | 93664 |
rs371823597 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122611834 | ACTAGAAAACCAAAT[C/T]CAGTGACAAATTTTA | 93664 |
rs371836914 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122448716 | TGATTGAGGCATCCC[A/G]TGCACAGAATTTCTC | 93664 |
rs371838424 | snp | A/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122541362 | CCACCACACCCAGCT[A/T]TTTTTTTTTTTTTTT | 93664 |
rs371842463 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122504502 | TGACACTCCATGTTT[A/C]TGACTTCTGTCTCCT | 93664 |
rs371851256 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122361381 | TGGAACTACAGGCGT[C/T]CGCCACCACACCTGG | 93664 |
rs371860461 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122776929 | ACAGAGGCAGGACGA[C/T]TGCTTGAGCCCAGGA | 93664 |
rs371869301 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122723614 | CCATTGTGGAAGACA[A/G]TGTGGCGATTCCTCA | 93664 |
rs371869589 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539921 | ATTTTCCTAATGTGT[C/T]CTTAATCTTCATAAA | 93664 |
rs371877711 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122711642 | CTATGAACTGTCACA[A/G]TATATGTTTTACATT | 93664 |
rs371883239 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122839757 | ACCAGTTAGAATGGC[A/G]ATCATTAAAAAGTCA | 93664 |
rs371900828 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122483128 | CAAAGCTTGAGAGGA[C/T]TGAATTGTTTCCAAG | 93664 |
rs371902477 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122378974 | ACCCTGCAGCTTTCT[C/G]TGTCTCTGAGAACAG | 93664 |
rs371904992 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122361295 | CTGGAGTGCAGTGGC[A/G]TGATCTTGGCTCACT | 93664 |
rs371908864 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122637874 | GCCAAGGCTCTGTAC[A/G]TAATCTTTATTTATG | 93664 |
rs371911426 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122580556 | AGTCTGAAGATGACC[C/T]TTCACACAGATTTAC | 93664 |
rs371911928 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122809292 | TAGACTGCCTCAGCC[A/G/T]GGCGCAGTGGCTCAC | 93664 |
rs371937717 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122836893 | AAGTTAACAAGGATA[C/T]CCAGGAATTGAACTC | 93664 |
rs371940890 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122517045 | CTTATGCCCTTTATG[A/G]TCAATCCCCTCCTTA | 93664 |
rs371951938 | snp | A/T | 0.000171985 | 0.00927162 | intron-variant | CADPS2 | GRCh38.p7 | 7:122451505 | AGAATCAATAATTCA[A/T]ATTGATCGAACATTT | 93664 |
rs371963779 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122675532 | ATGGGCATTCGGGTT[G/T]GTTCCAAGTCTTTGC | 93664 |
rs371971487 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122366656 | ACACACATATATATA[C/T]ATACACACATACATA | 93664 |
rs371976310 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122565231 | TGAATTTATAGAATT[-/A]AAAAAAAAAAAAACT | 93664 |
rs371987006 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122603035 | TAGAGATCCTTTGAC[A/G]GCTACACTTTAGCAC | 93664 |
rs371988246 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122790417 | AAAAAAAAAAAAAAA[-/G]AAAAGAATTAAGTTT | 93664 |
rs371996213 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122350405 | ATCTTTAATGCTCTG[C/G]CATTTATCAATTTCT | 93664 |
rs371998760 | snp | A/C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122725554 | TCACTTCCCTCCCCC[A/C/G]ACCCTCTCATTTTGA | 93664 |
rs372005134 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122464218 | GCTCAAAAACCAAAT[A/G]AGTGGGGCATATCAA | 93664 |
rs372005140 | snp | A/G | 1.80442e-05 | 0.00300363 | intron-variant, utr-variant-3-prime | CADPS2, RNF133 | GRCh38.p7 | 7:122697775 | TTAATACACTTCCTC[A/G]AAAGTCATGCCATCA | 93664 |
rs372005670 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122879728 | ATTATAAAAATCCAT[C/T]ACTAACTTGAAGGTA | 93664 |
rs372016803 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122398414 | AGTGGATTACTAGAA[A/T]GAATGATTTTTCTCC | 93664 |
rs372022587 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122679092 | CTTAAGAACAGGGTA[A/G]CAGTGATTTTCAGGG | 93664 |
rs372037719 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122723313 | ATCCAGAGTCTACAA[A/G]GAACTCAAACAAATT | 93664 |
rs372039624 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122565730 | TGACAAAATTATACA[C/T]ATTTACACTATACAA | 93664 |
rs372044967 | snp | A/C/T | 4.70248e-05 | 0.00484877 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554733 | ACGCATGATACGGAG[A/C/T]GTCTATGGGTTGGAA | 93664 |
rs372049171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122770020 | CCCATAAGATAGGAA[A/G]TACTAGCTCTGTTTT | 93664 |
rs372063244 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122490335 | GGATTGGCAGATTTT[C/T]GTCTCATTCACTAAC | 93664 |
rs372066757 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122740085 | ACAGAAAACACTTGA[G/T]GCTGGCAAGGATATA | 93664 |
rs372070330 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122351147 | GAGGTGGGCAGATCA[C/T]GAAGTCAGGAGATAA | 93664 |
rs372075308 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122518030 | ATCTAAGGCCAAAAT[G/T]ATTTCTATTTCAGAA | 93664 |
rs372077223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122757356 | GTTTCGCCAAGTTGT[C/T]CAGGCTGGTCTCAAA | 93664 |
rs372080489 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122533875 | CAGATCCAGTGCAGA[C/T]GTTAATTTGTTGCAT | 93664 |
rs372086455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122508972 | TGTAAATTTTAATCC[C/T]ATTTAAAGCATAAAG | 93664 |
rs372107276 | snp | C/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122884989 | TAATAAATGTCTGTG[C/T]ATGTAGGTATGCCTT | 93664 |
rs372108610 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122835970 | GCAACTCCAAGACAC[A/G]TAATTGTCAGATTCA | 93664 |
rs372121073 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122585894 | GGAGCCAAAATACAT[A/G]TTCATATCTTTTAAC | 93664 |
rs372146944 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122870844 | ATCTGTTCAAATATT[G/T]CCTCAATATTTGTTG | 93664 |
rs372147013 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122456152 | TTTAGTGTTTAATTT[A/T]ATTTTAATTAATAAT | 93664 |
rs372159687 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122720934 | AACAAAAAAGCTATC[A/C]TTTGAAATATATGTG | 93664 |
rs372173005 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122448306 | AGCTCTCATGAGACT[C/G/T]GCTCATCATCATGAG | 93664 |
rs372181487 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122394879 | TGAAAACAGAGAAAA[A/T]GGTTAATACTCAGTT | 93664 |
rs372196877 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122740804 | CATATAGAGAGTTCC[C/T]AGAAATTGATAAGAA | 93664 |
rs372200835 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122869863 | TAGAGTTTGTGCAAG[C/T]GATCAAAGTTATTAT | 93664 |
rs372204211 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122407362 | CCACTGGAGTGTGGG[A/T]GTCTCCCCGGGCTCC | 93664 |
rs372216834 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122754172 | ATTGCAATTAATTTG[C/T]TTTTGCTTTTCAAAA | 93664 |
rs372217285 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122572980 | GCATGCCAAGTACTT[A/G]CCAAATAATATAACC | 93664 |
rs372231180 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122786347 | AGTCAAGACACTGGG[A/G]TAAAGGACTGATCAG | 93664 |
rs372242558 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122360191 | TTTGGTATGATGATT[A/T]GCTTAAAAATGCTGC | 93664 |
rs372245609 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122809493 | GGCTGAGGCAGAGAA[C/T]TGCTTGAACCCGGGA | 93664 |
rs372247624 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122842257 | TCGACTACAGCCATC[C/T]ACAGGGGAAAGCCTC | 93664 |
rs372248816 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122345844 | ATTCCATAATTAAAG[A/C]AAATAAAAGTTTATT | 93664 |
rs372254449 | snp | C/T | | | upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122887121 | CTTTGAAAAGTCTCA[C/T]TCTGCTCTGCTGCCG | 93664 |
rs372271959 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122641833 | GTAACTACAAAAGTT[G/T]TGGCTCTCCAGGAGT | 93664 |
rs372274219 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122590996 | AAACTGCCTAACTTA[C/T]CACCATCATTGTTGT | 93664 |
rs372279130 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122638016 | AGCCTCTAACTCAGC[A/C]ATGTAGCTCTGTTGT | 93664 |
rs372290953 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122527801 | GAATGAACAGAGAAC[A/T]TTCATTACGGTAATG | 93664 |
rs372297376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122441299 | GCCATAATATGAGGA[C/T]AGGATTTCAGTGTGA | 93664 |
rs372298247 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122715710 | ACAACGCATTGCAAA[A/G]AAAAAAAAAAAGCCA | 93664 |
rs372298845 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122460128 | TTCATGTGACTTCTG[C/T]TTGCAGTATGGTGGA | 93664 |
rs372299800 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122571104 | AAGTATTTATATCAC[A/T]CTCTCATAAAGAAGG | 93664 |
rs372300012 | in-del | -/TC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122411086 | GCACACTGCCTATCA[-/TC]TCTCTCTCTCTCCAT | 93664 |
rs372306361 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122338579 | TTGGACATACTGGTA[C/T]AACAGTTAATTATTT | 93664 |
rs372309545 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122413329 | AGGAACTTAAACTAT[C/G]TTTCTAAGGAGAAAA | 93664 |
rs372321666 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122880624 | GAAATCAATTGGGAA[G/T]TTTTAACACTATACC | 93664 |
rs372342096 | snp | C/T | 3.67924e-05 | 0.00428892 | intron-variant | CADPS2 | GRCh38.p7 | 7:122491273 | TAAGAATTCCATGCA[C/T]ACATACATGGCAGGA | 93664 |
rs372353064 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122602909 | AATTTCATAACTCCA[G/T]AACAGGTAATAACAA | 93664 |
rs372355312 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122791212 | ACATCACAGTCTTAT[A/G]TAATAAATTATTCTC | 93664 |
rs372356272 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122753485 | TTGAGAACCTACTAC[A/G]TACCTGTACTCCTAC | 93664 |
rs372365106 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122430313 | CCTAAGGCGCAGTCT[C/G]CCCTTTTATATCTTA | 93664 |
rs372366344 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122386712 | GATTTGTATAAACAA[A/G]ACAGGTAGCTTTCCA | 93664 |
rs372367245 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122375061 | CAGACAACAAATAAA[C/T]AAAAAAATCCCATGT | 93664 |
rs372368460 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122485160 | TTAAAATTAGGCTAA[C/T]TAACAACCTGAAATG | 93664 |
rs372372682 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122878619 | CACTCCAGCCTGGGC[A/G]ACAGAGCAAGACTCT | 93664 |
rs372372999 | snp | A/C/G | 0.000364918 | 0.013503 | missense, utr-variant-5-prime | CADPS2 | GRCh38.p7 | 7:122621608 | TCCGGACCACCTTTC[A/C/G]AAACTGGAAGACTTT | 93664 |
rs372373866 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122832345 | TGCACACACACAATA[C/G]TAAGTAAAACTTTTA | 93664 |
rs372375318 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122362546 | TGTGAAGCATTTTAC[-/T]TTATTTAGCATGAAA | 93664 |
rs372378163 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122853313 | TCCTCCATTATTCCA[G/T]CCCCCTGTGGGGTAC | 93664 |
rs372379837 | in-del | -/CT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122679730 | CTTTAAAATTTCTCT[-/CT]TTTGTACTCTTTCCC | 93664 |
rs372382167 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122456951 | GCAAAAACTCTTTTA[C/T]ATACATTGAACATCC | 93664 |
rs372406566 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122407514 | CCCTCCCCATTTCAC[A/C]TATGAAAGAAAACGC | 93664 |
rs372408510 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122675408 | GTGAAAACTCTAAAG[A/T]GATGTTCTCTCCTTT | 93664 |
rs372410029 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122692308 | CACCCTTGGTGCCCA[A/G]CAGCTACTCATGCTA | 93664 |
rs372425497 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122348791 | CCAATTAGAATTGTA[A/G]TTCTTTAAAACACTT | 93664 |
rs372427305 | snp | C/T | | | intron-variant, utr-variant-5-prime | CADPS2 | GRCh38.p7 | 7:122617530 | ATAAAATAAAGTTGT[C/T]CTAGAAGTAAAAAGA | 93664 |
rs372429008 | in-del | -/ATAA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122619642 | CAAACAAATAAATAA[-/ATAA]GATAAACTCTTGTTG | 93664 |
rs372432926 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122503909 | TGATGAATTGTTTTG[C/G]AGGAAAACAAAGCAG | 93664 |
rs372442559 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539773 | TCTGTCTCTGTCTCT[C/T]TCTTTCTGTTTCTCT | 93664 |
rs372450803 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122322931 | CCTGGGTAGAATACA[C/T]TACTCTGCTGAACCA | 93664 |
rs372451757 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122447533 | CCATGTTGATTTCTT[G/T]TTTCGGGGAATTTTT | 93664 |
rs372454170 | snp | A/G | | | intron-variant, downstream-variant-500B | CADPS2, RNF133 | GRCh38.p7 | 7:122697689 | ACTGAAGTAACAAAA[A/G]AGGACACAAAAACCA | 93664 |
rs372454320 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122726461 | TATGTCAAGGTGAAG[C/T]CAGCCCCCACTGTGA | 93664 |
rs372480372 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122326076 | TAAAGTAGCGATGGC[-/A]AAAAAAAAAAAAAAA | 93664 |
rs372484743 | snp | C/T | 1.70269e-05 | 0.00291773 | missense | CADPS2 | GRCh38.p7 | 7:122663472 | GGCAAACTCCGCACA[C/T]GTTTTTCTATGTTTT | 93664 |
rs372487457 | snp | G/T | 0.000165986 | 0.00910854 | missense | CADPS2 | GRCh38.p7 | 7:122393531 | TAGCGGACAACCAAG[G/T]GTACAAAGATTTCTT | 93664 |
rs372491811 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122642041 | TCCCAGCACTTTGGG[A/G]AGCTGAGGCAGGTGG | 93664 |
rs372498485 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122575598 | TGCACCACCACACCC[A/C]GATAATTTTTGTATT | 93664 |
rs372499634 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122605804 | TTTATTAGATATGCA[C/T]CTCAATGAAATGGAT | 93664 |
rs372520381 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122335992 | TTTTTTCCCCTCCAG[A/T]GAAATATTTTGTCCA | 93664 |
rs372523851 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122493427 | TACAAAGTAAAAGGC[G/T]CAGGTCATTGTGAAA | 93664 |
rs372524069 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122769393 | ACAATTCTGAGGACT[C/T]ACTGAGCCCTCCAGG | 93664 |
rs372544073 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122716349 | GTCCACACTGCATAG[A/G]GCAGGCCCACCCCCT | 93664 |
rs372555114 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122387715 | GGTTTTTGAAAGGAA[C/T]TGCATCATGAGCAAT | 93664 |
rs372569644 | snp | C/T | 1.66095e-05 | 0.00288175 | missense | CADPS2 | GRCh38.p7 | 7:122438345 | ACTGCACTGACCTTC[C/T]ATTTTGGCATATTCT | 93664 |
rs372572074 | in-del | -/A/AA/AAA | 0.490727 | 0.0674567 | intron-variant | CADPS2 | GRCh38.p7 | 7:122337758 | AAACAAACTTTAAGG[-/A/AA/AAA]AAAAAAAAAAAAAAA | 93664 |
rs372572354 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122873629 | AGTGCTACAGTAAAC[A/G]TACGTGTGCATGTGT | 93664 |
rs372575809 | snp | A/G | 3.33689e-05 | 0.00408453 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122393577 | ATTTTCCATTACACA[A/G]AAGTGCTGAAATAGC | 93664 |
rs372576796 | snp | A/G | 0.00460326 | 0.0477539 | intron-variant, upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122621750 | AAATAATAGTGTTAC[A/G]TAAGTCATATTTCAA | 93664 |
rs372583702 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122746632 | TAAAACACACAGACA[C/G]ACACACACAGACACA | 93664 |
rs372584162 | snp | C/G/T | 1.65927e-05 | 0.00288029 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122701952 | GTACTACATCTTGGG[C/G/T]TTTGTATGTGTCAAA | 93664 |
rs372593185 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122328132 | ATACAGTAAAATGCA[C/G]ACACACACACACACA | 93664 |
rs372594960 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122568592 | CACAAAGATGTTAAG[G/T]AAATTCAGTGGAGAA | 93664 |
rs372608055 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122597773 | AACCAATCAAGTAAC[A/G/T]TATCTGATATGCTTT | 93664 |
rs372617298 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122797551 | ATTCTTTGCAGAGAC[A/G]TAGATGGAGCTGGAG | 93664 |
rs372617471 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122552470 | TTTAGTCTTGGGCAG[A/G]AGGCAATTGCAGGCC | 93664 |
rs372626483 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122479297 | CTGTAGCTGCATTTA[C/T]CACTACTCACATCTG | 93664 |
rs372630760 | snp | C/T | 0.000167986 | 0.00916323 | missense, utr-variant-5-prime | CADPS2 | GRCh38.p7 | 7:122736975 | AATAACTCCGAACTG[C/T]GTTGCAAAATGCTTC | 93664 |
rs372635119 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122562074 | TAATTCTACAGTGTG[G/T]TGTTTACTTAACAGT | 93664 |
rs372637509 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122883238 | CATAGAAACTCACCA[C/G]CTCTAATAGTGAACG | 93664 |
rs372645100 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122473976 | GTCCTTCTAAGAACA[A/G]AAGAGAGAAATGTGA | 93664 |
rs372655512 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122573870 | TGAAAAATCTCTGCA[A/G]TGACTGAACCTGCAA | 93664 |
rs372662595 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122399893 | GGGTTTCACCGTGGT[A/C]TCGATCTCCTGACCT | 93664 |
rs372665120 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122668174 | TAAAGAGGATTTGGG[A/C]AATAGAATGAATGTG | 93664 |
rs372667699 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122636289 | CTTGTAAGGGTAGTC[A/T]AGTGTTAATGAATTC | 93664 |
rs372668997 | snp | A/C/G | 0.000109353 | 0.00739368 | intron-variant | CADPS2 | GRCh38.p7 | 7:122491427 | TTGGCTAACCTGCTC[A/C/G]AGAAAAAAAAAGTTT | 93664 |
rs372672516 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122669989 | TCCCCAACATACAAC[C/T]TGTCCCTGAACCCTG | 93664 |
rs372673876 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122798390 | AGGCCATCTAAAGTC[C/T]GAAGTATTAACTGAA | 93664 |
rs372682041 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122696497 | TCCTCCTTTAGTCTT[C/T]CATGACCCCATGGTC | 93664 |
rs372695430 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122522513 | GTGTAATGGTAAAAT[A/C]GGGATATTTGGGATC | 93664 |
rs372706155 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122787025 | TAAGAAACGAACCTT[G/T]TAACAGTATGCAGGA | 93664 |
rs372734431 | snp | A/C/G/T | 0.000329683 | 0.0128357 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698468 | CAATCATAACCACAA[A/C/G/T]GACATCTTCAAATGC | 93664 |
rs372734597 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122822111 | GCTGATATCTCCTGG[C/T]GCTATCCCCAAACTG | 93664 |
rs372735375 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122366680 | ATACATATATATATA[C/T]ATACGTATATATATA | 93664 |
rs372746767 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122724360 | ACTCAGATTAATTGA[G/T]TGCTTAGTGTCTAGT | 93664 |
rs372747816 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122866866 | CCGAACATCTTACCA[C/T]GGCCTAAAAAATTCA | 93664 |
rs372748896 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122375845 | AAAATGGGAGGAAAT[A/G]TTTACAAACTATTTG | 93664 |
rs372774291 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122739411 | ACTACAATATTTGCA[A/G]TTTCTACATCATTAG | 93664 |
rs372785373 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122629608 | CAGTCCTAAATAGTT[C/T]CAGAAAGATGAAGCT | 93664 |
rs372787501 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122696938 | CAAAAGAAACATGAC[C/G]ATATCATAATAATAA | 93664 |
rs372795365 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122357304 | GGAGAAAAACTTTAT[C/T]AACCAGAGTACAATG | 93664 |
rs372803482 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122501688 | AATGTACCGTAGAGA[C/T]GGTAGTGAAACCCCA | 93664 |
rs372828732 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122472710 | GTTCACTCTATGTGT[C/T]TGTCCATGAAAAGAT | 93664 |
rs372841268 | in-del | -/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122720927 | ATTTCAAATGATAGC[-/T]TTTTTTGTTAAACCA | 93664 |
rs372848221 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122455729 | TTTTTATTTTTCAGA[A/T]GGAGTCTCCCTCTGT | 93664 |
rs372863094 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122524425 | ATACACTCTAAAAAA[A/G]TAATTAAGATGACAG | 93664 |
rs372865500 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122734388 | AAAAAAAAAAAAAAG[A/G]AAAAAAAAAAAGAAA | 93664 |
rs372878035 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122872631 | ATTTTGTAAGCCTTT[C/T]TAACTAAGCAGTATT | 93664 |
rs372899187 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122390932 | CATTCATTTCTAGAG[-/A]AAAAAAAAACAGAAT | 93664 |
rs372903848 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122335645 | TAGAAGGCTTGAAAG[A/C]ATCTTGTTCAGCCAC | 93664 |
rs372904731 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CADPS2 | GRCh38.p7 | 7:122355576 | CACAGAGTGAGGCTG[C/T]CTTATTAAAAAAAAA | 93664 |
rs372908613 | snp | A/G | | | utr-variant-3-prime | CADPS2 | GRCh38.p7 | 7:122318439 | TGTATCAAGGAAATG[A/G]ACATTTTATTGAAAG | 93664 |
rs372916725 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122762915 | CAAGAAAGAGAAAGA[C/T]AGGAGGTCATTGGGA | 93664 |
rs372922706 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122630618 | GGTTTAAAGTGTAGG[A/T]GTGATATGATCAGAT | 93664 |
rs372931344 | in-del | -/AAAAAA | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122559771 | GCGAGACTCCACCTC[-/AAAAAA]AAAAAAAAAAAAAAA | 93664 |
rs372957613 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122626101 | ATAAAGTCAGAGGGG[C/T]AAAAAAGACCAGATC | 93664 |
rs372957885 | in-del | AA/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122815623 | TAATGAAATACAAAA[AA/T]AATTCAAAATATATT | 93664 |
rs372958180 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122752059 | ACAGATGTCCAAGAA[A/C]ACTCAAGAACACTCA | 93664 |
rs372962096 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122662767 | ACATAGTTCAACTAT[C/T]ATCCTCAATTTATTT | 93664 |
rs372978327 | snp | C/T | 3.32204e-05 | 0.00407542 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122701898 | AAAGCCAGGGGTCAA[C/T]GCATGCCTTATGGAA | 93664 |
rs372983907 | snp | A/G | 0.000169986 | 0.00921759 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554720 | AACCCACATTTAAAC[A/G]CATGATACGGAGTGT | 93664 |
rs372985326 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122597768 | AAGCTAACCAATCAA[A/G]TAACGTATCTGATAT | 93664 |
rs372988473 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122467164 | ACCTGTCAGATCAGG[C/T]ACATTACCTAAGGAT | 93664 |
rs372988809 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122467656 | AGCCCTAGAAAACTG[C/T]AGAGGAGTCAGTGAA | 93664 |
rs372991972 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122787262 | CTGAAAATTTTATCA[C/T]TTGTGTTTTATGTCA | 93664 |
rs373030743 | snp | G/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554886 | TTTTGACAAATATGT[G/T]TTTTCACATTATCAC | 93664 |
rs373035998 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122397960 | AAATAACTTTTTTCC[C/T]GAAAAGATTCCATGT | 93664 |
rs373041659 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122339999 | GCACATTCACTTATA[A/G]TATTTTCATTATTTT | 93664 |
rs373041847 | snp | G/T | 1.65946e-05 | 0.00288046 | missense | CADPS2 | GRCh38.p7 | 7:122581226 | CTCCAGTGCTTTCTG[G/T]GAAGAGTTTCACTTT | 93664 |
rs373042621 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817797 | AACCTCGTATCTCTG[C/T]GCCCCAATCCCTTAT | 93664 |
rs373046038 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122574025 | AAATGGCAAAAAAAA[-/T]GTTTATCTTTACTAT | 93664 |
rs373046177 | snp | A/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122541859 | TATTCATATATATTT[A/T]TATATATGCATATAT | 93664 |
rs373049163 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122822489 | CCCCCAAAAATTTTC[A/G]CCACCCCAACACTTC | 93664 |
rs373061220 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122771881 | AACAGTGAGGTAAGG[C/T]GACACCATCATTTAA | 93664 |
rs373061385 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122742731 | CAGTAAGCCATGTTC[C/T]ATCTTGCTAGATGTA | 93664 |
rs373079366 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122490753 | CAATTAGTTAATATA[A/G]TCATAAATTTCTATT | 93664 |
rs373083760 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122480795 | GATATTCCTCAAACA[C/T]AGTATCATTAAAAAT | 93664 |
rs373085482 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122824608 | CTAATTTTTTGAAGT[C/T]CTTTACAAATAAATA | 93664 |
rs373093952 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122846156 | CATATTAAAATTAAA[A/G]TGCTAAGGATGTTCA | 93664 |
rs373099289 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122851813 | TTCAATTACCTCCCA[C/T]TAGATCCCTCCCACA | 93664 |
rs373105737 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122803673 | CATTTTAAAAATTTA[G/T]AGTATTCTTTGATGG | 93664 |
rs373109021 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122663610 | AACAAAAAACAATTA[C/T]AATTAGGTGTAGATG | 93664 |
rs373111282 | in-del | -/CA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122405139 | CAAAAAACAAAAAAA[-/CA]AAACAAAACAAAAAT | 93664 |
rs373111426 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122826812 | TACTGAAAGGAAAAT[C/T]TGTAGCATTAAATGC | 93664 |
rs373114112 | snp | C/T | 0.000165986 | 0.00910855 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122438411 | GAGACATTTTCTGAC[C/T]ACTTTCTTCACCTCT | 93664 |
rs373117383 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122838322 | ACCCACAGCCAATAT[C/T]ATACTGAATGGGCAA | 93664 |
rs373117979 | in-del | -/CTT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122644383 | CAATCTCCAAATCTT[-/CTT]GGAAGATGACAAACC | 93664 |
rs373118781 | snp | C/T | 1.87975e-05 | 0.00306568 | intron-variant, utr-variant-5-prime | CADPS2, RNF133 | GRCh38.p7 | 7:122698929 | TGCATCTCTCTCTTC[C/T]CCGAGTGACTTAAGA | 93664 |
rs373122777 | snp | A/C | 1.65737e-05 | 0.00287864 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122702473 | GCCTGTTTGGGCCTG[A/C]TGAAATTGGTCAAAG | 93664 |
rs373124975 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122614576 | AACCTGGTTGTTTCT[A/G]CTAGAGACCATGATG | 93664 |
rs373127517 | in-del | -/TA | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122541858 | ATATTCATATATATT[-/TA]TATATATGCATATAT | 93664 |
rs373133885 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122655260 | GGACTAATTCCAATT[C/T]TGAAAAATGTTCTTC | 93664 |
rs373134214 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122838382 | CACAAACAGGGATGC[C/T]CTCTCTCACCATTCC | 93664 |
rs373135821 | snp | A/C | 1.82257e-05 | 0.0030187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122393177 | ACACACCACCAGGAA[A/C]TAAGTGAGGAATACA | 93664 |
rs373138998 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122608653 | TTCTTATTGCTTCTT[C/G]TCTTTTTATTACTTT | 93664 |
rs373143022 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122873628 | TAGTGCTACAGTAAA[C/T]GTACGTGTGCATGTG | 93664 |
rs373155363 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122736042 | TATGTTATATACATA[C/T]TTAGTCAGCAAAACT | 93664 |
rs373156372 | in-del | -/AACTCAAGAA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122752059 | ACAGATGTCCAAGAA[-/AACTCAAGAA]CACTCAAAACGAATT | 93664 |
rs373158593 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122834361 | TCTACAGCTCCCAGC[A/C/G]TGAGCGACACGGGTA | 93664 |
rs373158677 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122630039 | TTACTCATGATACCT[C/T]TTCACCCATTCACTC | 93664 |
rs373164764 | in-del | -/AAGTT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122383543 | ATTCATTCTTAAGTT[-/AAGTT]TCTCCACATCTGCCC | 93664 |
rs373171401 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122658554 | GAAATACTATGCAGC[C/T]GTAAAAAAGGATGAG | 93664 |
rs373177332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122564718 | CACCTGCATGCCTAC[A/G]TTTATCACAGCGTTA | 93664 |
rs373181814 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122486230 | GCTATAGCTGCCATA[A/C]ATAGTAATTCCTATG | 93664 |
rs373184579 | snp | C/T | | | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122699998 | TATTAGAAGATTCCA[C/T]AGGCTCTGTCCACTC | 93664 |
rs373196944 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122599822 | ACAGTATATACTATA[C/T]TCTGTGTTACTTTAA | 93664 |
rs373200204 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122758317 | AAAGAAAAGTTCAGG[A/C]TGAAAATAAAGCAAA | 93664 |
rs373207009 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122709763 | TCCTTTGTAGGGACA[G/T]GGATGAAATTGGAAA | 93664 |
rs373213538 | snp | C/T | 1.6736e-05 | 0.0028927 | missense, utr-variant-5-prime | CADPS2 | GRCh38.p7 | 7:122736990 | CGTTGCAAAATGCTT[C/T]GTCAGCTACAATTTG | 93664 |
rs373215466 | snp | C/T | 9.02649e-05 | 0.00671746 | intron-variant | CADPS2 | GRCh38.p7 | 7:122615318 | AAGATAAAATGATTT[C/T]AAAATAATGCATCAA | 93664 |
rs373219693 | snp | C/T | 8.14332e-05 | 0.00638044 | intron-variant, utr-variant-5-prime | CADPS2 | GRCh38.p7 | 7:122885979 | AGTGGTGGTAGGAGG[C/T]GCCCGGTCCCGCAAC | 93664 |
rs373230461 | in-del | -/G | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122432662 | AAAAAAAAAAAAAAA[-/G]AAAAAAAGAAAAGAA | 93664 |
rs373232950 | snp | A/G | 9.89462e-05 | 0.00703302 | intron-variant | CADPS2 | GRCh38.p7 | 7:122491292 | TACATGGCAGGAAAA[A/G]TGATTCAATTAAGAT | 93664 |
rs373235184 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122792523 | TTCTGTTGTTTATAA[A/G]CTACCCAGTTTATGG | 93664 |
rs373254243 | snp | A/G/T | 1.67913e-05 | 0.00289748 | intron-variant, missense, synonymous-codon | CADPS2, RNF148 | GRCh38.p7 | 7:122702628 | AAATGTTATATTCAG[A/G/T]TGAGCTGTCCAAATG | 93664 |
rs373258762 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122387669 | TTTTATGTCACTTAC[A/T]TTCTCTTTCAAAAAC | 93664 |
rs373271067 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122639166 | GTAATCCTCATTTTA[C/T]GTAATGTTAGAATTG | 93664 |
rs373288423 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122389260 | GAACTGGAAATAAAA[C/T]GGGCTAGGTAGGGAA | 93664 |
rs373288610 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122497188 | AATTTAAAAAAAAAT[C/T]TCTTCAGTCTCAATT | 93664 |
rs373289206 | snp | C/T | 2.05501e-05 | 0.00320541 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122407616 | CGGTTGAGCCTCTAG[C/T]GCAGTGTCCATATCC | 93664 |
rs373309915 | snp | C/T | 0.000165986 | 0.00910855 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122701963 | TGGGGTTTGTATGTG[C/T]CAAAGCAAACAACAC | 93664 |
rs373310582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122759778 | AAAGCAACTTATCAT[C/T]GTAATTTGATTTTAA | 93664 |
rs373315669 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122451672 | TGGAATGGAATTATT[A/C]TCTTTTAGACAGCCT | 93664 |
rs373319465 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122425040 | GCTGGGGTGCAGTGG[C/T]GTGATCATGTCTCAC | 93664 |
rs373325116 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122329381 | CCGGGCGGGATCCAC[A/G]CAGCTGTAAAGGGCT | 93664 |
rs373345383 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122694062 | TTACAACTTGAGTAA[C/T]AGCTGACTGTTTAGA | 93664 |
rs373360370 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122480506 | ATTCTACCTATATTT[C/T]GCTTCATCAATTGGG | 93664 |
rs373370029 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122536094 | ACCTAAATTTTATAA[C/T]GTAAATTTATCTCCA | 93664 |
rs373372031 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122325101 | ATTCTTCTGGCAAAT[A/G]TAGTACAAAAGCCCT | 93664 |
rs373385294 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122519396 | CAACAACAACAACAA[C/T]TGCCTGCTTAACTTT | 93664 |
rs373388802 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122398662 | ATCACAGAAACAGAA[A/G]ATATGAATATGGGCT | 93664 |
rs373389567 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122360429 | TATCATTATTCTACC[A/T]TCTATAAGAAACCCA | 93664 |
rs373393424 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122688452 | GAGGTCTGGAGGGAG[C/T]GGGTGGATGAGTGGC | 93664 |
rs373395567 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122770091 | CCAAGAACATCAACT[A/G]TAACTGAGGGAACAA | 93664 |
rs373405685 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122798010 | GCAGGTTTTTTTTTT[-/T]CAATGTTATATATCA | 93664 |
rs373405973 | in-del | -/GTC | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122847612 | ATTTTTTTTTTTCTT[-/GTC]ATCATTAACAACAGT | 93664 |
rs373436405 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122576333 | ATCACTTGGTTATCA[A/G]GAGAGTATTGGCAGC | 93664 |
rs373466142 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122709963 | CCTAATGCTAAATGA[C/T]GAGTTAATGGGTGCA | 93664 |
rs373476432 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122409322 | TCCAGTTCACAGCCA[A/T]TATCTTTGCAAAAGG | 93664 |
rs373478363 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122326565 | TTAGAAAATGACAAA[A/G]GAGTTTTGAAAGACA | 93664 |
rs373485616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122716544 | TAGGGTCGGGGGAGC[A/G]GGGAGGGATAGCATT | 93664 |
rs373490886 | in-del | -/TAGT | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122388146 | GATGTGGACAGAAAA[-/TAGT]TAGTAATCCCAGAAC | 93664 |
rs373506457 | in-del | -/TC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122666049 | CCTCATCTAATCACT[-/TC]CWTTGAGCAGTGACA | 93664 |
rs373510427 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122656256 | CCAAAAAAGATCCCT[C/G]TATGGCCATGGCAGA | 93664 |
rs373515332 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | CADPS2 | GRCh38.p7 | 7:122369410 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCGCC | 93664 |
rs373522900 | in-del | -/CT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122828372 | TTATCCACTCTATCT[-/CT]GTTTTTTGTAAGCTT | 93664 |
rs373524375 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122625129 | AATCTCGGCTCACCA[C/G]AACCTCCGCCTCCCA | 93664 |
rs373535147 | snp | A/G | 0.000163239 | 0.00903287 | intron-variant | CADPS2 | GRCh38.p7 | 7:122663206 | TTCCACGAGTCAGAC[A/G]GGGGAAGGGAAAATA | 93664 |
rs373542690 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122821912 | AAGCTCCTGTATAGA[C/T]GCTCCTTTTTATTAG | 93664 |
rs373549854 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122374791 | GACGAGCTGATGGGT[A/G]CAACAACCACTATGG | 93664 |
rs373551722 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122644447 | ATGACACAGCCTTCA[C/T]AGTTGTCTTACTGTG | 93664 |
rs373562637 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122724084 | CCTAATGTAAATGAC[A/G]AGTTGATGGGTGCAG | 93664 |
rs373586029 | snp | A/G | 0.311614 | 0.242289 | intron-variant | CADPS2 | GRCh38.p7 | 7:122819666 | TAGTTATCCCCACCT[A/G]CCCAGTTCCCTTATT | 93664 |
rs373596363 | snp | C/T | 1.65952e-05 | 0.00288051 | missense | CADPS2 | GRCh38.p7 | 7:122320197 | CGTCACTGTCTTTCA[C/T]AGTAATGCCCTGAAG | 93664 |
rs373604366 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122816872 | CATTCCACCACAAAA[A/G]AAGTGTAAATGGCCG | 93664 |
rs373615148 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122775871 | TCAAATTTAATCATA[A/G]GTTCTGCTAGTTTCA | 93664 |
rs373617470 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122859644 | TTTGTTATCCATGAG[G/T]GATAGGTTCCAGGAC | 93664 |
rs373622878 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122684965 | AAAGCAAAATGAACC[C/T]AAAACTTAACTAAAT | 93664 |
rs373630400 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122672954 | CCTTCAGATGTTCAG[A/C]TGTGTCCGGAGTTTC | 93664 |
rs373637688 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122715721 | AAAGAAAAAAAAAAA[-/A]GCCAATTGTACAAGT | 93664 |
rs373643348 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122756904 | GACTCCCTCTCAAGG[-/A]AAAAAAAAAAAAAAT | 93664 |
rs373644916 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122577036 | ATAATGCTGGGATTA[C/T]AGGCATGAGCCACCA | 93664 |
rs373646395 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122608823 | ACTGATATTTAATTG[C/T]CTACTGTGATTATCA | 93664 |
rs373648936 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122472889 | CTCTCTGAAGTATCC[C/T]CATTTTGATTTCAGA | 93664 |
rs373653402 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122771048 | AGTTAGAATCATGGG[C/T]TTTTTGAAAAATGCC | 93664 |
rs373655488 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122750763 | TAAAAAATGCAGGTA[C/T]GAAAGACCTACCCCA | 93664 |
rs373661891 | snp | A/G | | | utr-variant-3-prime | CADPS2 | GRCh38.p7 | 7:122319890 | TCATGTTCTGATCAC[A/G]AGCAGAGCCAAGGTT | 93664 |
rs373664210 | snp | C/G/T | 6.59113e-05 | 0.00574038 | intron-variant, synonymous-codon | CADPS2, RNF133 | GRCh38.p7 | 7:122698610 | TCCCCGTTCAATAAG[C/G/T]GCAAGCCAGGTCTCT | 93664 |
rs373664903 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122721286 | AACAAAATTGATAGA[C/T]TGCTAGCAAGACTAA | 93664 |
rs373672780 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122451211 | GAATGATACGCTGAG[A/C]AGCAGACCACAGACT | 93664 |
rs373685681 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122739182 | GCTCTGGGAATGCCA[A/C]GAAGAGCTTCTCCTT | 93664 |
rs373685887 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122720154 | CGTCATACTAAAAGT[A/G]TCAATCAGACCTAAC | 93664 |
rs373686268 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122884514 | TTCTCCAACATGAGG[A/G]GTCTCCCTACCATTC | 93664 |
rs373686482 | snp | A/T | 1.65737e-05 | 0.00287864 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122702141 | AATCTAAGTAAAAGT[A/T]GGCAATTGTGGCAGC | 93664 |
rs373688254 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122649972 | TGGAGTGCAGTGGTG[A/T]GATCTCGGCTCACTG | 93664 |
rs373692074 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122728702 | CAACTGGAGGGAGCT[A/T]TGTTTTTATTTTTTT | 93664 |
rs373696377 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122635521 | ACCTATGAGTGAGAA[C/T]ATGTGGTGTTTGGTT | 93664 |
rs373702464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817489 | GACCCAAAACTCTGG[C/T]GCCGGTCACAGACTG | 93664 |
rs373707445 | snp | A/G | 0.00033172 | 0.0128744 | intron-variant | CADPS2 | GRCh38.p7 | 7:122407699 | ACCAGGCAAATGCCT[A/G]CAAAAGGATAAAAAC | 93664 |
rs373709705 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122767887 | TAGAATTCTGGGATG[C/T]TAACTGTGACACGGA | 93664 |
rs373710547 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122349583 | CCATGAGCACAAAGG[A/G]ATCAAGAACTATGGG | 93664 |
rs373711740 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122750792 | CACACCTACTATTTC[A/G]GAATTTTGAAAAGAG | 93664 |
rs373713155 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122582540 | CAAAGAGACTTTTTG[A/C]AATTTCATATAATTA | 93664 |
rs373715380 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122321780 | CCACAGCACTCAGCC[A/G]TGTTCACTTTTTAAA | 93664 |
rs373717674 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122391205 | CCTAATGTTGATAAC[C/T]TTGGTAGGTAAAGAT | 93664 |
rs373720022 | snp | G/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122552775 | CTATGATAGGTTCCT[G/T]TTTTTTTTTTTTTTT | 93664 |
rs373727641 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122519983 | ATTAGCATATCTCAG[C/T]ACCTACAATCTTTTT | 93664 |
rs373729393 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122669455 | CTCACAGGTGTCCTA[G/T]GATGCTGATAACTGT | 93664 |
rs373730065 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122855632 | ATTTGGAAAACAAGA[C/G]ATGCCATGGAAACAG | 93664 |
rs373733220 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122605046 | TTGTCCTAAATACTG[C/T]AGACAACTGTAACAC | 93664 |
rs373734880 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122591249 | CAATTGCTTCAAAGC[A/G]AATAAAATACTTAGG | 93664 |
rs373744353 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122718659 | CAGGGAACTGATCAA[A/C]TGGGGCCGTGTTAAG | 93664 |
rs373750217 | in-del | -/CA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122625784 | CTCTCCCTGCCCTCC[-/CA]CACACACACACATAT | 93664 |
rs373764661 | snp | A/C/T | 4.17319e-05 | 0.00456773 | intron-variant | CADPS2 | GRCh38.p7 | 7:122325463 | CAATTCATATCTAAA[A/C/T]ACATTTTGTTTACCT | 93664 |
rs373779783 | snp | C/T | 1.72415e-05 | 0.00293606 | missense, intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554643 | GGAACTACCATTCGG[C/T]GTAATTCAGCTGATT | 93664 |
rs373788415 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122658228 | TGGCAATCATTAAAA[A/T]GTCAGGAAACAACAG | 93664 |
rs373789014 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122354315 | AGAGGTGTAATTACA[C/T]CTCCATTTTACAGAA | 93664 |
rs373817343 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122803019 | TTTCTAAAAAAATAT[G/T]AATTATATTTAAAGG | 93664 |
rs373818219 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122579422 | AGTAAGGGAGCATAA[C/G]CGGTTTCTCAGATAT | 93664 |
rs373820869 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539769 | TCTCTCTGTCTCTGT[C/T]TCTCTCTTTCTGTTT | 93664 |
rs373823504 | snp | A/G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122395034 | TTACTAAATCTAATT[A/G/T]CTAGCAACTCCAATA | 93664 |
rs373831705 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122831682 | GTGAAAAATTCATCA[C/T]TCTCCCAATAAAGCA | 93664 |
rs373838665 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122711818 | CCACCACACCCGGCT[-/A]ATTTTTGTATTTTTA | 93664 |
rs373849392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122660053 | GAAATTTGAATCTAC[A/G]TAAAGAAATGAAAGA | 93664 |
rs373858945 | snp | G/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122538363 | TTAATTAGGTTTTTT[G/T]TTTTTTTTTTTTAAA | 93664 |
rs373862801 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122457690 | ATTATTTAGTGCTGA[C/T]GAGCATCCGTTCTAT | 93664 |
rs373868606 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122767239 | CCTGGGTTTTAGACA[C/T]TAAACTAAAAAGCAT | 93664 |
rs373869050 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122330372 | AACATTAATGCACTA[C/T]AATTTCACCAGTATA | 93664 |
rs373873525 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122492085 | GCTGAGGTAGAAGAA[C/T]TGCTTGAACCTGGGA | 93664 |
rs373878671 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122684614 | CCACAATGGATGAGA[A/C]ATCAATAAATACCAG | 93664 |
rs373878733 | snp | C/G | 0.000183123 | 0.00956703 | intron-variant, utr-variant-3-prime | CADPS2, RNF148 | GRCh38.p7 | 7:122701800 | TGTATTTGGAAAGAT[C/G]TGGTTACATCTTCAG | 93664 |
rs373896948 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122587463 | TTCCTTTTTATGGCT[A/G]TATGGTATTCCATGG | 93664 |
rs373901124 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | CADPS2 | GRCh38.p7 | 7:122727287 | TGTGTTAGCTCTAAA[A/C]TGAGCAGCCTTTCCT | 93664 |
rs373904819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122714182 | ATTGTTCTAGTAGTT[C/T]CTATTTATTTGGTAA | 93664 |
rs373915267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122738382 | AAATAAGGCGTCTTA[A/G]ATCTTAGGTAATGCA | 93664 |
rs373921969 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122841622 | AGCTTTGCCGCAAGA[A/G]TAGGAGAAAACACAA | 93664 |
rs373924229 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122569168 | TCCTTAAGCTGATAA[G/T]CAACTTCAGCAAAGT | 93664 |
rs373940033 | snp | A/C/G | 0.000125603 | 0.00792385 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122702725 | ACAGAACTATGCGTC[A/C/G]AAGGGGTAATTCTAA | 93664 |
rs373943472 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122385361 | AAATATAAATTATGG[C/G]CAAATAGCTAATGTC | 93664 |
rs373955103 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122533046 | CCCCCATTTTTAGAA[A/G]GGCCTATCACTCTTG | 93664 |
rs373970321 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122476110 | TTATAAAATTGGAAG[A/G]TTCTTTTGTATTTTA | 93664 |
rs373970338 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122847912 | GGTTGAAAGCAATAC[A/G]GTAGCAAAGCCAGTA | 93664 |
rs373975209 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122393776 | TATAATTAGCCTTCT[A/G]TATATGGCTGTCAAA | 93664 |
rs373976405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122692609 | GCGGCCACATAGCCG[A/G]CCCAAGACCCCTCAG | 93664 |
rs373980449 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122324370 | AGAAAATATTTTAAT[G/T]TGGCTAGAAACATCT | 93664 |
rs373995629 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122415341 | TAGGGGGAAAAGCAC[A/G]TGATGCAGCATTGTA | 93664 |
rs373995792 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122480924 | GGAACTATATACTTA[C/T]ACAACTAGACATTTA | 93664 |
rs373997742 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122513787 | AATGTGCCTGCACCA[A/G]TCTCAGTCTCCATGT | 93664 |
rs374007279 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122639284 | ATTTATTTTCGACAT[A/T]ATTTATTTAATTGGA | 93664 |
rs374015148 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122343918 | GCCAGCTGGATGGAT[A/G]ATAATTTTTCTACCC | 93664 |
rs374017442 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122789996 | AAGAAATTCTACATG[A/T]TCACATAAGAATAGG | 93664 |
rs374018454 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122328524 | GTATGGGAATGGCAT[C/T]ACTGCTTTATTCTTT | 93664 |
rs374026812 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122732038 | TCATTCCTCAGTATA[C/T]GCTTTTATGTAACAT | 93664 |
rs374045153 | in-del | -/CT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122862501 | CTTCCATCAGAAGGC[-/CT]CTCTCTCTCATGGCT | 93664 |
rs374046476 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122718517 | AAGGGTAGCCATGGC[C/T]TTCTAAACAGGGAAC | 93664 |
rs374056936 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122548073 | ATCAATCCCTCTTCA[A/G]ATAAAGCAATTTAGC | 93664 |
rs374087775 | in-del | -/AATTACACTGA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122449241 | AGCAAAAAAGAGGGA[-/AATTACACTGA]TTTTCATTGAAAGAT | 93664 |
rs374089555 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122765478 | TGGGAACTAATGAAT[C/T]ACAAGTGCCTATCTA | 93664 |
rs374093006 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122442350 | TTTTGGAGCTCCTTG[C/T]TTTGCTGAACCAGAT | 93664 |
rs374104804 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122653896 | CATTTCTTTCCCTCC[A/G]CTCAGCCCTGCCTAT | 93664 |
rs374116074 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122599999 | CAGATTATATTCCTC[A/G]TAATATATCTTAATT | 93664 |
rs374120928 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122744701 | TAAACTAAGTGATAA[C/G]TACAGAACAGCAAAC | 93664 |
rs374124308 | in-del | -/AC | 0.0193772 | 0.0965046 | intron-variant | CADPS2 | GRCh38.p7 | 7:122763023 | CAATAGTAGATGGAA[-/AC]ACACACACACACACA | 93664 |
rs374127914 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122611445 | AATAAATTAGAGAAC[A/T]TGGATGAATTGAAAA | 93664 |
rs374135705 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122555934 | AGCAAGACTCCCCTT[C/T]TCTCTAGGAAAGACA | 93664 |
rs374140217 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122346374 | CCCTGTCTCAAACAA[A/G]CAAATGAAACAAAAT | 93664 |
rs374147366 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122587591 | ATGCATGCATGTATC[G/T]TTGCAACAGAATGAT | 93664 |
rs374150060 | in-del | -/CATA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122607053 | AAAAGCACCTACATA[-/CATA]GACATTTCACGCCTT | 93664 |
rs374166513 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122602986 | GGCTGCAAAATTACT[A/G]TCAACAACTGCAGGC | 93664 |
rs374173314 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122645364 | GTGTGTATACATGTA[C/T]ATGTATACACACATA | 93664 |
rs374173470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122725520 | GTGTACACGTACCCA[A/G]TAGGTAGTATTTCAT | 93664 |
rs374176638 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122499178 | CAAACACAAGATTAA[C/T]TGCCCAAGGGCAGAT | 93664 |
rs374178378 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122463934 | ATTCCAGTTGGAGAC[A/G]TCAGTATGAACTCAT | 93664 |
rs374180635 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122474625 | GCAGAAGACTACCTT[A/T]TATCACATGAAATAT | 93664 |
rs374181164 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122705958 | ATAATATATAATATA[-/T]TATATAATATAATAT | 93664 |
rs374199999 | snp | C/T | 0.000464291 | 0.0152292 | missense | CADPS2 | GRCh38.p7 | 7:122474391 | CTCACCAAGCAAGAA[C/T]AGGAATCATTCAGTC | 93664 |
rs374201307 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122538143 | CCACTTATACAAATT[C/T]AGTAAAAAAAAAAAG | 93664 |
rs374203344 | snp | G/T | 1.69902e-05 | 0.00291458 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122360948 | GAATGACAGAATGGA[G/T]GAAAAGAAAGTGCCT | 93664 |
rs374207763 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122713344 | AACTTAGGCAACCTA[C/T]CTAAACTCATGTGCC | 93664 |
rs374211810 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122363860 | TTACTTAGTGACAAA[G/T]AGGAATGAGTTTGGT | 93664 |
rs374230817 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122761314 | GAACATGGGCAGCCA[A/G]GCCAATACTCATCTC | 93664 |
rs374240743 | snp | C/T | 3.29832e-05 | 0.00406085 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122697910 | GAGAAACTTCATTAT[C/T]TGTCTCCTCTTCACT | 93664 |
rs374249322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539909 | CCTTTTTTTTCCATT[C/T]TCCTAATGTGTCCTT | 93664 |
rs374258729 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122839380 | ATGGGCAAGGACTTC[A/G]TGTCTAAAACACCAA | 93664 |
rs374260315 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122445674 | GAAAATATTATCTGC[A/G]CATGGTGGCATGTGC | 93664 |
rs374262402 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122492455 | TGCTTGGATCACAAG[A/G]CCATATTTGAACAAA | 93664 |
rs374265410 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122465893 | TTTTGTACGTCAACA[C/T]AGATCTACAAATATC | 93664 |
rs374265963 | snp | A/G | 8.31594e-05 | 0.0064477 | intron-variant, synonymous-codon | CADPS2 | GRCh38.p7 | 7:122393225 | AGAAGGCATCCACGA[A/G]GCAGTAGAAATGTTA | 93664 |
rs374270715 | in-del | -/GT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122449869 | CAGCACTAAATGACT[-/GT]CCCTACCCCTGGTTA | 93664 |
rs374275718 | snp | C/G | 1.72243e-05 | 0.0029346 | missense | CADPS2 | GRCh38.p7 | 7:122451404 | TGATTTTCTAAAAGG[C/G]AAGAGAGTCTCTCTT | 93664 |
rs374277912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122727439 | GATTTACTTACCCAC[A/G]GCCCACCTATATAGA | 93664 |
rs374295936 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122552105 | AACTGTCCCTGTCCA[C/T]AGGGAGCAATTACTA | 93664 |
rs374303898 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122458102 | CACCTGCTTCTGCTA[C/T]GAGGAATGAGGAATG | 93664 |
rs374304218 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122506027 | AATTGTACTCAGACC[G/T]GTATCAGTTGGCACT | 93664 |
rs374310640 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122354185 | ACAATGTAGATACTA[G/T]ATTTTATTGTAATCA | 93664 |
rs374315887 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122757794 | AGTCATTATTCACAC[A/G]ATACTGCTTGTGCAT | 93664 |
rs374321046 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122610938 | CTGGGGCTTGTATTC[C/T]CTGCAGCTAAGAATC | 93664 |
rs374329379 | snp | A/C/G | 0.000161987 | 0.00899817 | synonymous-codon, missense | CADPS2 | GRCh38.p7 | 7:122387038 | TACCTCTTGTCCTCC[A/C/G]TCCAGGGCACAGAGT | 93664 |
rs374331556 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122788297 | ACTCAGAATGAAGCA[G/T]TTCATTTTTGTCTGG | 93664 |
rs374337152 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122837282 | ACATTTAAAGCAGTG[A/G/T]GTAGAGGGAAATTTA | 93664 |
rs374338544 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122569627 | CACTACCTGACTTCA[A/G]ACTATACTACAAGGC | 93664 |
rs374338750 | snp | A/G | 1.70067e-05 | 0.002916 | intron-variant | CADPS2 | GRCh38.p7 | 7:122621458 | TATGCTGTCAGAGGT[A/G]AGCATGAGATAAAGC | 93664 |
rs374346775 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122760649 | AAAAAATGATGAGTT[A/C]ATGTCCTTTGTAGGG | 93664 |
rs374346990 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122536888 | CATTGATGATAGTAA[G/T]GAAATGCCTGATGAA | 93664 |
rs374350855 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122730174 | AATGAACATGTAAAT[A/G]GGACATAGGACATGA | 93664 |
rs374355729 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122543662 | AGATTATCTGGGAAC[A/G]CAATTTGGGATTCCC | 93664 |
rs374355995 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122590032 | ATTTAAGATGTTTGC[A/G]CTATGCAAAATGACC | 93664 |
rs374359479 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122855115 | CTGTAGTCAGGGTGG[A/G]AGAAGAACACTGATG | 93664 |
rs374368310 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122858676 | GATAAAAGCATTAAT[A/G]TTTGAAACACGTTAT | 93664 |
rs374373037 | snp | C/T | 4.52008e-05 | 0.00475377 | intron-variant | CADPS2 | GRCh38.p7 | 7:122379493 | TGGACACAAAACTTT[C/T]GTCATCAGTCATAAA | 93664 |
rs374376030 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122487880 | AGAAGAATGAGATTA[A/G]ATGTATTCATAAAAA | 93664 |
rs374378861 | snp | G/T | 0.000437904 | 0.0147905 | intron-variant | CADPS2 | GRCh38.p7 | 7:122480185 | TTTTATATATCCAGA[G/T]AGTCAAAGAAAAAAA | 93664 |
rs374380569 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539764 | CTGTCTCTCTCTGTC[C/T]CTGTCTCTCTCTTTC | 93664 |
rs374389061 | in-del | -/A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122393078 | ATAAAAAAAAAAAAA[-/A/G]CAGTATTCCTCAACC | 93664 |
rs374411337 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122465724 | AGGTTGAGGACCACT[A/G]GTTTAAAAGATGAGA | 93664 |
rs374420443 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122627580 | GAGTTTATGAACACA[C/T]CTTCTTCTCAGTCAT | 93664 |
rs374444906 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | CADPS2 | GRCh38.p7 | 7:122318946 | TTAATAAATGCAGTA[A/G]CACAATCTGCCAATA | 93664 |
rs374459325 | in-del | -/AGAA | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122432341 | TGAAGCAGTATAAAT[-/AGAA]AGCCTTTGGGACAGG | 93664 |
rs374466187 | in-del | -/TA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122759985 | TATATAGGTGTATTT[-/TA]TATATATATATATAT | 93664 |
rs374472751 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122877655 | ATTATAAATGCAAGA[A/G]ATCTATATGATGAAA | 93664 |
rs374475184 | snp | C/T | 0.000167986 | 0.00916323 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122701860 | GATGTCACACTTGCA[C/T]ATGGGACATGTCCTA | 93664 |
rs374477892 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122502106 | AAATCACTAAAGGTG[A/T]TGGAGAAAGAGAAAA | 93664 |
rs374485850 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122581656 | TTGCTCAGGGTTTGT[C/T]TACGTAAGAGAGAGT | 93664 |
rs374491909 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122457968 | CCACCCCATCTCCAA[A/C]TCATCAGGTAAGTTT | 93664 |
rs374493268 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122816106 | TCATGCTACTGAACA[C/T]TAGATCTTATCCTTT | 93664 |
rs374495851 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122882680 | ATAAGTCTAACAAAT[C/T]GCCTTTATTAATTAG | 93664 |
rs374498678 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122386032 | TTAAAATTCTAAGAG[A/G]AGTTTATAAATTCTG | 93664 |
rs374500771 | snp | A/G | 4.96899e-05 | 0.00498422 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122393446 | AGATACCTACTTGAC[A/G]GGCTGCCATGTCTCC | 93664 |
rs374504784 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CADPS2 | GRCh38.p7 | 7:122368130 | GTGATCTGCCTACCT[C/T]GACCTCCCAACGTAC | 93664 |
rs374509729 | in-del | -/GCATCCCAAA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122705007 | AGCCTGAGGAGAGAA[-/GCATCCCAAA]ACTCTCCCAACCCCG | 93664 |
rs374510459 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122674274 | GCCCAGAGAGTGGCT[A/C]CCACAGCGCAGCGGT | 93664 |
rs374513409 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122639920 | CTCTGATCTTCCAAG[C/T]GTGTATCTATAGCAC | 93664 |
rs374526407 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122493524 | AGATAACATTTCATT[A/T]GAAAAAATGCTGATT | 93664 |
rs374537959 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122670869 | GTGAAACCCTGTTTC[-/A]AAAAAAAAAAAAAAA | 93664 |
rs374547662 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122852371 | CTCTGCCCTCATGCA[C/G]CTTACATTTATGTGT | 93664 |
rs374557120 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122569316 | ATACTTAGGAATCCA[A/G]CTTACAAGGGATGTG | 93664 |
rs374564632 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122593428 | CCAAGAGACAGATTC[G/T]GGGCTTGGAAACCAC | 93664 |
rs374566818 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122606745 | TGGCTGGTGCTAATG[C/G]GGAAAAAGAAGGTAT | 93664 |
rs374569753 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122573299 | GTAATCCCTACACTT[C/T]GGGAGGTTGGGATGG | 93664 |
rs374571560 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122642594 | TTGCTCTTCTAGTAC[A/T]TTAAAAACTATGAAC | 93664 |
rs374580767 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122436251 | TCATCAAGTTGTGTA[A/C]ATTAAATATGTACAG | 93664 |
rs374585601 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122483057 | GTTGGTCCAGAAATG[A/G]GGAAAATGCATCCTG | 93664 |
rs374588052 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122437443 | TTTGGTAAAACTATA[-/C]TAATATCAACTGCTT | 93664 |
rs374588491 | snp | A/G | 3.39784e-05 | 0.00412165 | synonymous-codon, intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554555 | TTATACTCACCCACT[A/G]TGCTTCATATGTGCT | 93664 |
rs374592911 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122590185 | AAACAAACAAAAAAA[-/A]CAAAGTGGAATGCAT | 93664 |
rs374601386 | in-del | -/C | 0.311123 | 0.242413 | intron-variant | CADPS2 | GRCh38.p7 | 7:122820929 | TAATACTTTTAGAGG[-/C]CCTCAAAATCACAAA | 93664 |
rs374607731 | in-del | -/CAA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122664436 | ATAAAATAAAAACAA[-/CAA]TAGAGACAACCATAG | 93664 |
rs374610259 | in-del | -/AA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122705887 | ATAATATAATATAAT[-/AA]ATATAATATAATATA | 93664 |
rs374613109 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122592396 | CTGTTGGTGGGACTG[C/T]AAACTAGTTCAACCA | 93664 |
rs374616311 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122476289 | GTTAAAAATAATGCC[C/T]ATTAATGGTTAATCT | 93664 |
rs374621775 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122835505 | TAAAGGCAGAAGTTC[A/G]AACCCAACGCAAAGA | 93664 |
rs374621925 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122794931 | ACTAATGAGAACAAA[G/T]ATACAACATACCAGA | 93664 |
rs374628282 | in-del | -/TGA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122386344 | GAAAAAAAAAGATGA[-/TGA]AAGAGAACAGAAGGG | 93664 |
rs374645259 | in-del | -/GTAA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122669376 | TTTTTTTGAGAAAAA[-/GTAA]TTACTACCCCCACAC | 93664 |
rs374655477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122597360 | TTAGTAAATAAATGC[C/T]TGTTCTTAATTTACC | 93664 |
rs374656947 | in-del | -/TACA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122441040 | ATTTAAGGTAACACA[-/TACA]CTGGAATAATTGAAA | 93664 |
rs374673556 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122636762 | GTAAGCCACCAAACT[C/T]GGTCTGCCTTTTTAA | 93664 |
rs374677954 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122696244 | TCAGTGTGGTCCCTC[A/G]TCCCTCAGGAAATGA | 93664 |
rs374678864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122349790 | ATTATATGCTGCAAA[C/T]GCTCTTGCTTCCTGC | 93664 |
rs374682900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122585045 | GGGAGGAAATGCTAA[C/T]GAACACCTCCTGTGA | 93664 |
rs374694331 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122664923 | CCAAGTAGCTGGGAC[A/C]TGCAAACACACACCA | 93664 |
rs374705758 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122489154 | ATGAGTATGGTCTGT[A/G]GTTTCTAAAATAAAG | 93664 |
rs374716260 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122648553 | GTGCCCGAGTAGAAC[A/G]GGCACTGTGTTAAAA | 93664 |
rs374717481 | in-del | -/CA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122652797 | TCTAGGTGCTACTTA[-/CA]TTGTTTTTATTCTTT | 93664 |
rs374725326 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122458983 | TATATTGTAACTAAA[A/G]GACTTCATATATATC | 93664 |
rs374747275 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122500311 | TGGCACAGAGTCACT[A/G]CTTCTGTATTTTGGC | 93664 |
rs374747948 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122627591 | CACACCTTCTTCTCA[C/G]TCATGAACCTGAGAA | 93664 |
rs374753602 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122761607 | AAAACCACCACCCTA[G/T]TCTTACTTTATCTGA | 93664 |
rs374765268 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122366329 | ATACGAGGCGGCCAG[G/T]TGTGGTGGCTCACAC | 93664 |
rs374770355 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122824606 | TCCTAATTTTTTGAA[G/T]TTCTTTACAAATAAA | 93664 |
rs374777887 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122586905 | TACAGTGAGTGCTTT[C/T]AAAAATTATTTGTCA | 93664 |
rs374782185 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122871180 | GAGATTGCCACAGTG[C/T]TGGGAAAAAAAAAAA | 93664 |
rs374787317 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122769650 | GATAAAATAAAAACT[A/T]AAAATGTCCTAATTA | 93664 |
rs374790937 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122790523 | CCCTGGCCAATTTAA[C/T]TGTTGCAAATAAAGA | 93664 |
rs374803362 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122790625 | CTCTTATGAATAAAA[C/T]ATCCAACTTAATCCA | 93664 |
rs374825003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122362272 | GCTTACGTAGCAGTT[A/G]TGGAGAGAAAACAGA | 93664 |
rs374828266 | snp | C/T | 0.000475234 | 0.0154075 | intron-variant | CADPS2 | GRCh38.p7 | 7:122736922 | CCTTTTAAAATGCAT[C/T]GGAAAGCCAAAAACA | 93664 |
rs374828462 | snp | C/G | 0.000172703 | 0.00929094 | intron-variant | CADPS2 | GRCh38.p7 | 7:122393629 | AGAGGGATAATATCA[C/G]ACATTTGGAAAATAT | 93664 |
rs374834556 | snp | A/C/G | 0.000434619 | 0.0147352 | intron-variant | CADPS2 | GRCh38.p7 | 7:122581301 | CCCATCTGTAATGAA[A/C/G]TAAAAAAAATGTTTC | 93664 |
rs374839557 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122643916 | GGCAACATGGCAAAA[A/C]CCCTCTCTACTAAAA | 93664 |
rs374840873 | snp | A/C | 7.71635e-05 | 0.00621094 | missense | CADPS2 | GRCh38.p7 | 7:122416121 | CTCTGCCAGATGAAG[A/C]ATCTCTTCCAGCTTT | 93664 |
rs374842234 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122327497 | CCTAACATAACATAC[G/T]GGTTACTCTGTTAGA | 93664 |
rs374844853 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122607164 | AAAGGGACTAAAGTC[C/T]CTTTTTCCCACTACA | 93664 |
rs374845453 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122705879 | TATTATATATAATAT[A/T]ATATAATAAATATAA | 93664 |
rs374866808 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122639422 | CCCAGTTTTCCCTAA[C/T]GATAGCACCTTATAA | 93664 |
rs374880538 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122840272 | CATCACACACCAGGG[A/C]CTGTTGTGGGGTGGG | 93664 |
rs374881938 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122691296 | CCATGAATGCACCCA[C/T]CTGCTATTACTAACT | 93664 |
rs374888620 | snp | C/T | 0.130008 | 0.219321 | intron-variant | CADPS2 | GRCh38.p7 | 7:122570017 | CAATGGCAACAAAAG[C/T]CAAAATTGACAAATG | 93664 |
rs374896288 | in-del | -/ATATAT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122579451 | ATAAAATTGCATCGA[-/ATATAT]ATATATATATATATA | 93664 |
rs374900313 | in-del | -/AAAG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122826575 | ATGAATATAAAATAG[-/AAAG]CCTCAGCAAAGGAAA | 93664 |
rs374902142 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122614441 | ATTGGTATTATAATA[A/C]GGCAAAATCCTAAAT | 93664 |
rs374911817 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122593789 | GCAAAGGAGAAAGAG[A/T]GAGGAAGAAAAAGAA | 93664 |
rs374914513 | in-del | -/CAT | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122562694 | TTTTAAATTTCTCCT[-/CAT]AAGTGTGTGATTTAA | 93664 |
rs374915680 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122550636 | TAACCTTTGAATTAG[A/G]AAAATAATTTTATTT | 93664 |
rs374920940 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122454219 | ATAGAATTTTAAATA[C/T]GTGTCTGGTATTTTG | 93664 |
rs374926038 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122490576 | AAATGCATAGCACAA[A/T]CTGATATTTCATGCC | 93664 |
rs374930183 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122583227 | TTATGCATTAAAATA[C/T]TTTTATACAATGATA | 93664 |
rs374935544 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122442810 | AACAGAATATCACAT[C/T]TATCATTGTATTTAC | 93664 |
rs374936779 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122678066 | AGTGTCTAGTATCAT[C/T]AGACACTCAAATTTT | 93664 |
rs374939312 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122555195 | AGCACATTTTCTGCT[A/G]TAGATCAATACCAAA | 93664 |
rs374941404 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122406150 | TATTACAAATGATTT[C/T]ATGTCTATGTGATTT | 93664 |
rs374955101 | snp | C/T | 8.30862e-05 | 0.00644486 | intron-variant | CADPS2 | GRCh38.p7 | 7:122438318 | CTCTCACTGCCACTT[C/T]GACAATTGCTCACTG | 93664 |
rs374955906 | snp | A/G | 3.31554e-05 | 0.00407144 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122663342 | AAGTTCAGACACTGC[A/G]CTTAGGGCCATTCTA | 93664 |
rs374966675 | snp | A/C | 0.000167986 | 0.00916323 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122702660 | CTTTTCCGTTTGAGT[A/C]AGGAAAGCTAAGTAG | 93664 |
rs374969271 | in-del | -/TTTG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122526207 | TTATTTATTTATTTA[-/TTTG]AGGCAGAGTCTCACT | 93664 |
rs374972832 | in-del | -/CAA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122782366 | TGCTCATTACTGAAA[-/CAA]CACCAGTAGCAAATC | 93664 |
rs374975382 | snp | C/G/T | 0.0093653 | 0.0677938 | intron-variant | CADPS2 | GRCh38.p7 | 7:122393411 | GGTTGAAGAGGCAGG[C/G/T]GCTCTACGGACACTA | 93664 |
rs374980807 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122722387 | ATCACAAGCATTCTT[A/C]TACACCAATAACAGA | 93664 |
rs374992114 | in-del | -/TAA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122371995 | TTAGAGGAACAATAA[-/TAA]CAATATCAACTAATA | 93664 |
rs374992568 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122668764 | TTTTATCATCACCAG[A/G]TCACTTTTGACAGAC | 93664 |
rs375004933 | in-del | -/TC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122865161 | CTCTCTCACACTCTC[-/TC]GTTTCTTCTCTCACC | 93664 |
rs375007141 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122485869 | TGAAGCCAATGTTTA[C/T]TAACCATTTTGAAAA | 93664 |
rs375008840 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122415621 | AAAAAAAAAAAAAAA[-/G]AAAAGCCCAGTGGAA | 93664 |
rs375015916 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122465467 | CAGCAGGAGGTGAGC[A/G]GCAGGCAAGCGAGTA | 93664 |
rs375016709 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122337506 | CTTTTAGGCAATTGG[A/G]CATGCTTATCTCAAG | 93664 |
rs375018324 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122518857 | AATGAGTACTGTGAA[C/T]TTTTTTCACGTGATT | 93664 |
rs375021611 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122747912 | AAGAAATCTCCTTCT[C/T]TCTGCTGCCCCCAAA | 93664 |
rs375050557 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122580946 | GACTGAGTTGGTGAC[A/G]AGGAATTTGTATTTA | 93664 |
rs375050997 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122821659 | ACAGTCTGATAACAG[A/G]TGAGCCTTTATTAGT | 93664 |
rs375053945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122853469 | CCCTTTGTTGCTTTA[A/G]CCCAAAGGGTGGTAA | 93664 |
rs375057872 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122822039 | GTTCTCAACTACTCA[C/T]ACACGCCCTGCTCTT | 93664 |
rs375061455 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122879119 | GTGCACACCTGTAAT[C/T]CCAGCTACTCGAGAG | 93664 |
rs375072040 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122549240 | TGTCTCTACCCTGTC[C/T]CTAATACAAAAAAAT | 93664 |
rs375074086 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122366681 | TACATATATATATAT[A/G]TACGTATATATATAT | 93664 |
rs375081297 | snp | C/T | | | intron-variant, upstream-variant-2KB | CADPS2, LOC105375481 | GRCh38.p7 | 7:122529007 | CTTTTATTATTAATA[C/T]CAAGTTTTGTACTTT | 93664 |
rs375081598 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122624884 | TAAACAAGGAAATAA[C/T]TTCTTCTGATAGAAA | 93664 |
rs375081835 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122864293 | CAAGGCTAAAAATGT[C/G]TTATCTGTCATACAC | 93664 |
rs375089203 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122691607 | CATCAACAAGATCAT[G/T]ACATATGATGAGGCT | 93664 |
rs375111256 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122366658 | ACACATATATATACA[C/T]ACACACATACATATA | 93664 |
rs375125664 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122617727 | TCTGCTAGCCTAATA[C/T]CAATGAAAGAATTCA | 93664 |
rs375127026 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122346480 | TAAATTTTTTATTAA[C/G]CTGAGTAAAATATTT | 93664 |
rs375133730 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122588160 | CTCCCACTCTGTAGG[C/T]TGTCTGTTCACTCTG | 93664 |
rs375137637 | in-del | -/A | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122740145 | GGAAAGCAAAATGGT[-/A]ATAGCTACTTTGTAA | 93664 |
rs375142528 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122485286 | AGCCAAGATAGGCTG[A/C]AAGCGAGGCCTTTTG | 93664 |
rs375149994 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122461634 | GGAGTCTCGCTCTGT[C/T]ACCAGGCTGGAGTGT | 93664 |
rs375152888 | snp | A/G | 4.35e-05 | 0.00466349 | intron-variant | CADPS2 | GRCh38.p7 | 7:122325622 | GGAGGAGAACAAAAA[A/G]AGAAAACAACCTCTG | 93664 |
rs375162034 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122820875 | ACCTTACTGTTTTAG[C/T]CTAGCCCTCATGTCT | 93664 |
rs375171615 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | CADPS2 | GRCh38.p7 | 7:122398770 | TCTCTCTCTCCCGCC[A/G]CCCTCCCCACCCCTC | 93664 |
rs375175333 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122537619 | GGGATATAAGAAATA[C/T]TGGGAAAAATAAGCT | 93664 |
rs375176420 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122403729 | AATATTAATTCATTG[A/G]AATTAATGATATTCC | 93664 |
rs375183393 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122380902 | TGATATTTTTGCTTT[C/T]GAGATAGCTTGAAGA | 93664 |
rs375186524 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122675656 | AAAAAAGAATGAGTT[C/T]ATGTCCTCTGCAGGA | 93664 |
rs375192300 | snp | A/G/T | 3.3144e-05 | 0.00407076 | missense | CADPS2 | GRCh38.p7 | 7:122393542 | CAAGGGTACAAAGAT[A/G/T]TCTTGCAAGTGTTTG | 93664 |
rs375192592 | snp | A/C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122361383 | GAACTACAGGCGTCC[A/C/G]CCACCACACCTGGCT | 93664 |
rs375193068 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122481899 | ACCTGTAATCCCGGC[G/T]GCTGAGATTACTTGG | 93664 |
rs375195926 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CADPS2 | GRCh38.p7 | 7:122373964 | ACTGCCAGAAAAGAA[A/G]ACTATAAGCCAAGAT | 93664 |
rs375203024 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122880112 | AGTTTGCCCACTAAC[A/G]GTTTTGTAGGACCTT | 93664 |
rs375215728 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122603059 | TTAGCACAGCAGATA[C/T]AAATCTTCAATGACA | 93664 |
rs375227046 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122768803 | AGCCCAAAGACCCCA[C/T]GTGTAGAAAGCCACA | 93664 |
rs375239223 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122811863 | AAGGACATTTTATTA[C/T]ATGACACTGTGCTAA | 93664 |
rs375255331 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122825895 | AAGGTCAAGTGGGAG[C/T]GTAGAATTCTGCTCT | 93664 |
rs375257836 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122871818 | GACATGGACCATCCT[A/G]GTTTTCTTCTAATAC | 93664 |
rs375261369 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122637913 | TTTGCCTTAGGTTTC[A/C]CAGGTGCTGTATGCT | 93664 |
rs375263959 | snp | G/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122545453 | AGGAGTTCGTGTTGG[G/T]TATAAAATCTAGACG | 93664 |
rs375274601 | snp | C/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122562094 | TACTTAACAGTCTCT[C/G]AAAATCTATGAAACT | 93664 |
rs375281164 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122705540 | TGTATTATCTATATT[A/G]TATATTATATATATT | 93664 |
rs375290968 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122773522 | ATACTGTGCATTAAA[C/T]ACTATGAAACAATGA | 93664 |
rs375295041 | snp | C/T | 1.65663e-05 | 0.002878 | intron-variant, synonymous-codon | CADPS2, RNF148 | GRCh38.p7 | 7:122702412 | CACGTTGATTTTATG[C/T]GTAAAAGTACAGCCT | 93664 |
rs375300593 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122792960 | TAAAGCATTCATATT[A/G]GATCTTTGTTCAAAG | 93664 |
rs375308215 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122436601 | ATGAGCAAGCATTTT[A/G]TTGTTGCTATTTTTT | 93664 |
rs375327403 | snp | A/G | | | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122703704 | TGTTTCAAAATGTTC[A/G]CTTTGGTTGCTTTAT | 93664 |
rs375327971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122565828 | AGCAAATTTTCAAGC[A/G]TATAATTCATGATTA | 93664 |
rs375330366 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122761936 | CCAGGAGGCAGATGT[C/T]GCAGTTAGCCATGAT | 93664 |
rs375336639 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122681140 | GTTGTAGGGTGGGGG[A/G]AGGGGGAGGGATAGC | 93664 |
rs375339419 | in-del | -/TAA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122594380 | TAATGACTTTCATAA[-/TAA]GAAAAATCCTGCAAG | 93664 |
rs375342406 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122644247 | ACCTTTCTAGCCTCT[C/T]GGATAATTGCATTAT | 93664 |
rs375348715 | snp | C/T | 0.000167986 | 0.00916322 | missense | CADPS2 | GRCh38.p7 | 7:122629254 | ATAATTTACCTTTGC[C/T]ATTTTATCTGCCAAT | 93664 |
rs375349065 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122394024 | AAGAGGTAAGCTTGA[G/T]GACTTGTAAAAGCTA | 93664 |
rs375376829 | in-del | -/AAGAGGTGTAATTACATCT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122354299 | TCACAATAAGCCTAT[-/AAGAGGTGTAATTACATCT]CCATTTTACAGAAGA | 93664 |
rs375378309 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122624135 | TTTCATTAACTCTAT[G/T]CAGCCTGCTTGTGTT | 93664 |
rs375412692 | in-del | -/GT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122620129 | AAAAAATTGAAAACT[-/GT]TCTTCGTAAGACTGT | 93664 |
rs375416961 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122706845 | ACACACACACACACA[-/T]TTTTTTTTTCCAGAA | 93664 |
rs375420213 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122567174 | AGATAAAATATCACA[C/T]GAATTATGTAAAAAC | 93664 |
rs375421338 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122688341 | AATTCACTTGCCACT[A/G]CCTTCATTTATATTT | 93664 |
rs375427143 | snp | C/T | | | intron-variant | CADPS2, RNF148 | GRCh38.p7 | 7:122701225 | ATACGATTAAGAAAA[C/T]GTGGCACATATACAC | 93664 |
rs375436996 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122442841 | TGCTAAAAATGTCCT[A/T]TCTTAATCTTGCTGC | 93664 |
rs375437393 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122841915 | CAATAGGAAAGAGAT[A/G]GGATACTCAAAATGG | 93664 |
rs375437989 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122815393 | TTTATCCCACATCTG[A/G]AAAAGCCGATAACAG | 93664 |
rs375450033 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122705947 | ATATTATATAATATA[A/T]TATATAATATATATA | 93664 |
rs375454306 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122411289 | GCAGCGGCACAATCT[C/T]GGCTCACTGCAACCT | 93664 |
rs375462512 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122811573 | AAGATTAAGATAATA[C/T]ACCTGCCAGCAGAAA | 93664 |
rs375466106 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122824010 | CATGCAAAAGACATT[G/T]GCTTGTACTTTCCCA | 93664 |
rs375482220 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122655427 | ATCCACATCAAGGCG[A/C]GACCCTCTACCAGCA | 93664 |
rs375487279 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122508716 | CACAGAATAAAAATA[A/T]ATGAAATGATTCCAT | 93664 |
rs375487586 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122552615 | GGAACTGCCAGGTAA[A/G]AGCAAGGGTTTCTTC | 93664 |
rs375488164 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122333889 | TTTATAAATATAAAT[A/T]TATATATATATATAT | 93664 |
rs375490584 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122645526 | TACTTATATATATAT[A/G]AGTATATATATATAC | 93664 |
rs375496320 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122589629 | GGTGGCTGCTGACAC[A/G]TCGTTTACTATGATC | 93664 |
rs375522714 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122716451 | AAAGCTAACAGCCTA[A/C]AAGAGCAGGGGTAAG | 93664 |
rs375523459 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539730 | AATCTTATAACTCTG[C/T]CTGTCTGTCCCTCTC | 93664 |
rs375529507 | snp | C/T | 1.66807e-05 | 0.00288792 | missense | CADPS2 | GRCh38.p7 | 7:122663463 | TCTATTTCTGGCAAA[C/T]TCCGCACACGTTTTT | 93664 |
rs375538673 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122447074 | ACCACATTCCCCCAC[C/T]ATAAACAAAATTCCT | 93664 |
rs375554189 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122425690 | GCTGAAACTGATGAA[C/T]AGTCCCCTCCCTGGT | 93664 |
rs375556792 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122369616 | GTTAATATCCTCCTT[A/G]ACATCTCCTCCCTCA | 93664 |
rs375562105 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122796536 | AAACCAATGGAACAG[C/G]ATACAGAGCCCAGAA | 93664 |
rs375572733 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122332732 | TAACACAATAAGTTC[A/G]AAAACAGGACAAGTT | 93664 |
rs375574512 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122618247 | AAAGTAATCCTGAAC[A/G]GCTGTTTTTTTGATA | 93664 |
rs375595966 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122819987 | GGCCTTTATAAAGCC[C/T]ATAAACTCTCCTTAC | 93664 |
rs375600598 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122846243 | CTCCAAGGAATAAAA[A/G]GATATAAAACTGATT | 93664 |
rs375603217 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122509266 | GACATCCCACTAACA[A/G]AGTGCCTCTCATACA | 93664 |
rs375603251 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122881286 | TATCAAAATCGCAGC[C/T]GATTTCATTTTTGAA | 93664 |
rs375610541 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122679686 | ATCACGGAACCTGCC[A/G]ACATATTATGTCTCC | 93664 |
rs375611868 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CADPS2 | GRCh38.p7 | 7:122860596 | CCCAAGGATAAAGAA[C/T]ATTAAAACATTTAAG | 93664 |
rs375613781 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122630780 | TTGGGAGAAAAACTA[A/T]ACAAAAGGCCTGAGA | 93664 |
rs375615861 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122802412 | TGTACCTCCACTCTT[A/C]GGTAATCGCTGGTCA | 93664 |
rs375621818 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122851752 | CAGATCTCATGAGAC[G/T]TATTCACTATCATGA | 93664 |
rs375624206 | snp | C/T | | | utr-variant-3-prime | CADPS2 | GRCh38.p7 | 7:122318495 | GTACAGAGCAATGTG[C/T]CGTGGAACAGCAAGC | 93664 |
rs375625167 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122838726 | CAACTTACAAGGGAT[A/G]TGAAGGACCTCTTCA | 93664 |
rs375627532 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122728886 | ACCCAAGTATTTATT[A/C]TATTACAAGTCGCCT | 93664 |
rs375630670 | in-del | -/TC/TCTC | 0.418974 | 0.184249 | intron-variant | CADPS2 | GRCh38.p7 | 7:122398738 | AAAGGAAAACACTCT[-/TC/TCTC]TCTCTCTCTCTCTCT | 93664 |
rs375631522 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122514484 | ATACTGTTTGCCCCC[-/C]TCCCCCCTTTAGAAA | 93664 |
rs375638340 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122564639 | CTAAAAATAGAAATA[A/T]CATTAGATCCAGCAA | 93664 |
rs375643293 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122526146 | CTGCAGTTGCTCACA[A/T]GGATAAACACTGTGT | 93664 |
rs375655013 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122637045 | TTTATTTTTTTAAAT[A/T]GTTTATTTATTTTTT | 93664 |
rs375655737 | snp | A/G | 1.66032e-05 | 0.0028812 | synonymous-codon, utr-variant-5-prime | CADPS2 | GRCh38.p7 | 7:122621639 | CCAAATTGGCCATTA[A/G]CAAATTCACTGAAGA | 93664 |
rs375656346 | snp | G/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122557380 | ACACTTCCTTGGCAG[G/T]GTGTCTTCACAGTGC | 93664 |
rs375700390 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122332579 | CATTGGGAAGGTTGG[C/T]ATAAAATAGGCACCT | 93664 |
rs375702706 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122870185 | AAAAAGAAGATGCAA[A/C]TACCCAACTATATGC | 93664 |
rs375710544 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122541223 | TTTTTTTTTGAGACG[A/G]AGTCTCACTGTTGCC | 93664 |
rs375711040 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122582791 | GCATTCTCTTATAAC[C/T]GAAATAAAAGATTTT | 93664 |
rs375715669 | snp | C/T | | | utr-variant-3-prime | CADPS2 | GRCh38.p7 | 7:122320028 | CTTTTACTCTACATT[C/T]AGGCTTACTTTTTAA | 93664 |
rs375719114 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554286 | GGTGCCCTGTATCAA[C/T]ATGACTGATGAGTAA | 93664 |
rs375727026 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122511601 | TTAAGACCTATGCTT[C/G]CTAAGTTAGCTGGGT | 93664 |
rs375739348 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122392935 | GATTTACTTAGGGTA[C/G]AATGCCACCAAATTA | 93664 |
rs375748246 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122423154 | TTTATCTAGATTTTC[C/T]GACCCTTCCTCCAGC | 93664 |
rs375750162 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122368069 | AATTGTTATCTCACA[G/T]GGTTTTGCCATGTTG | 93664 |
rs375751091 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122865162 | TCTCTCACACTCTCT[C/T]GTTTCTTCTCTCACC | 93664 |
rs375768300 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122809830 | AGAGCTTGTTGCCTA[A/T]ATATACAACTCTAAA | 93664 |
rs375769413 | in-del | -/AACT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122731141 | ATTAAATACCTCTCT[-/AACT]CTCATTTATTCTTTG | 93664 |
rs375772729 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122598907 | GAGAGACAACTAGAG[C/G]AAACAGTGAGAGTTC | 93664 |
rs375783744 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122618583 | TGCACTTTATTCCTT[C/T]GACTCAGTATAGTTC | 93664 |
rs375791498 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122609413 | AAACAATTCCTCCGT[-/T]ATCTCATTCATACAA | 93664 |
rs375794714 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122572083 | CTCCTCGTGAAATCA[G/T]AATCACAGGTATTTT | 93664 |
rs375798841 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122658114 | CAAAAGAAGACATTT[A/G]TGCAGCCAACAGACA | 93664 |
rs375812025 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122476649 | GATAGCACTTTGAGT[C/G]ACAAATACAGACTCT | 93664 |
rs375827339 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122720913 | ATTGGCAGTTTCATA[C/G/T]GGTTTAACAAAAAAG | 93664 |
rs375832317 | in-del | -/T | 0.0205511 | 0.0992634 | intron-variant | CADPS2 | GRCh38.p7 | 7:122587000 | CAAATGCATCACTAA[-/T]TTTTATAACAGAAAA | 93664 |
rs375843762 | in-del | -/AGAAA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122879575 | AGAAAAGAAAAGAAA[-/AGAAA]TGGGGAAAAGGACAC | 93664 |
rs375844465 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122409881 | CTCAGAAATGCATCC[A/C]TCTACAGGGTACTAA | 93664 |
rs375850370 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122654418 | CAGGCTGACTCTCTT[A/G]TTAGTGGCTAATGAA | 93664 |
rs375851709 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122378378 | TAGGAAAGGTGAGTG[C/T]CTTGCCTCACCTGAA | 93664 |
rs375854893 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698038 | TCACATTTGCAAATG[A/G]GGCATGTCCCATGGG | 93664 |
rs375872047 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122361247 | TTTTTTTTTTTTTTT[-/A]AAATGAGATGGAGGC | 93664 |
rs375872678 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122697146 | CACTAAAATAGTTGC[C/T]GTTCACTTAAAGAGT | 93664 |
rs375874525 | snp | A/G | 0.000367242 | 0.0135457 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122471554 | GACTTGGCCAGGGCT[A/G]AACCATCCCTGCAAA | 93664 |
rs375882337 | in-del | -/GAGACG/TGAGACG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122369155 | CCTTTTTTTTTTTTT[-/GAGACG/TGAGACG]GAGTCTCGCTCTGTC | 93664 |
rs375891367 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122641538 | CAAAAGGGTGATTAA[C/T]TGAAAAGAGATAAAG | 93664 |
rs375896798 | snp | A/T | 6.71141e-05 | 0.00579246 | missense, utr-variant-5-prime | CADPS2 | GRCh38.p7 | 7:122736981 | TCCGAACTGCGTTGC[A/T]AAATGCTTCGTCAGC | 93664 |
rs375904629 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122795158 | GACATAAAAAAAAAA[-/A]TTCAAAAGATCAACA | 93664 |
rs375916828 | in-del | -/CAAAA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122331655 | AAAAACAAAACAAAA[-/CAAAA]AAACAAACAAATAAT | 93664 |
rs375917250 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122480532 | TTGGGTGTTTTTTTA[C/G/T]GTAGTGAAAATAATA | 93664 |
rs375938953 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122841510 | TGTATAAAATATGCT[A/G]TAGTAGTGATAAATT | 93664 |
rs375944288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122601674 | TTTTAATTTGGAAGA[C/T]GTGTAAGTGCAAAAA | 93664 |
rs375954936 | snp | A/G | 0.000263632 | 0.0114781 | intron-variant | CADPS2 | GRCh38.p7 | 7:122416188 | AAAAAAATCATAATC[A/G]TGTTACCTTGAAAAT | 93664 |
rs375964322 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122322106 | TTATTACCACAAAGA[A/T]TTGTGTTTATTCCTA | 93664 |
rs375968902 | snp | C/T | 1.65952e-05 | 0.00288051 | intron-variant, synonymous-codon | CADPS2, RNF148 | GRCh38.p7 | 7:122701959 | ATCTTGGGGTTTGTA[C/T]GTGTCAAAGCAAACA | 93664 |
rs375972871 | snp | A/T | 1.65721e-05 | 0.0028785 | missense, utr-variant-5-prime | CADPS2 | GRCh38.p7 | 7:122621558 | TGTCCAAAAATGCAG[A/T]GTTCTGTGAACGTTT | 93664 |
rs375983647 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122597269 | GAAACACTAATAAGT[C/T]CTGCCTCACATAATT | 93664 |
rs375999090 | snp | A/C | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122556622 | ATTTTGGCTGATCCA[A/C]AAATTAAAGGCTATC | 93664 |
rs376022156 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122812685 | TTGCTTTCTTTATGA[C/T]AGGACCAATGTCTTA | 93664 |
rs376022213 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122722396 | ATTCTTCTACACCAA[C/T]AACAGACAAACAGAG | 93664 |
rs376025552 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122767557 | GTCAATAGTTGAGAG[A/G]CATTCAAACGCATAC | 93664 |
rs376026055 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122760546 | AATGTAGAGAGTTCA[C/G]TACCATCCCTAGTTA | 93664 |
rs376036183 | snp | C/T | 2.38444e-05 | 0.00345277 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554735 | GCATGATACGGAGTG[C/T]CTATGGGTTGGAACT | 93664 |
rs376038466 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122849532 | CGGTCCCCAGCTGTC[C/T]GCAACATCTTTATCA | 93664 |
rs376040672 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122457071 | GAGTAAACAGCATTA[C/G]TCATCCTAATCCATT | 93664 |
rs376050628 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122425953 | TAACTCTTTTTTCCA[C/T]ACTCAAGGAGAATGT | 93664 |
rs376064003 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122620872 | TGCTATTTCTACCCA[C/T]GTGCGTTTTGATGCT | 93664 |
rs376067953 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122399014 | TGGTAATATTAATGT[A/G]TACATTAACTAGTAT | 93664 |
rs376096783 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122569314 | AAATACTTAGGAATC[A/C]AGCTTACAAGGGATG | 93664 |
rs376100885 | in-del | -/CTTTTC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122713671 | CTTTTCCATATATAA[-/CTTTTC]CATATATTCTTGAAG | 93664 |
rs376102679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122771528 | ATTTTTCCTCTCAAG[A/G]AATTTCCAGTGGAGA | 93664 |
rs376112510 | snp | A/G | 8.91162e-05 | 0.00667459 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554514 | CTGAAATGAAATTCA[A/G]TAATTCAGGAAAAAA | 93664 |
rs376116430 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122692196 | AAGTCTGTACATGAC[C/T]GCCGACATTACTTGC | 93664 |
rs376117431 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122780521 | CACCACCCTGTCCCA[C/T]CAATAATCCGATTTA | 93664 |
rs376123272 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122418209 | TTCTTGAGAGCCAAT[C/T]ATGTGTCAGGCACAA | 93664 |
rs376128381 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122751216 | ACTCCTGAGCTCAAG[A/G]GTTCCTCGAGCCTTG | 93664 |
rs376128597 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122847747 | ACCCACATAGTCTTA[-/A]CTGGTTACTGCTCCG | 93664 |
rs376136201 | snp | A/C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122705745 | TATTATATAATATAT[A/C/T]ATATATATAATATAT | 93664 |
rs376144676 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122680294 | TGTTTTATCTAAAAA[A/G]TAAATTTTGTTAAGA | 93664 |
rs376170031 | snp | A/T | 0.021333 | 0.101051 | intron-variant | CADPS2 | GRCh38.p7 | 7:122723441 | AATGCTCATCATCAC[A/T]GGCCATCAGAGAAAT | 93664 |
rs376170857 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122553628 | TTTGTTTCCCCTAAT[A/G]GTCATCTAAAGAATC | 93664 |
rs376175054 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122592581 | TAGCAAAGACTTGGA[A/G]CCAACCCAAATGTCC | 93664 |
rs376198038 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122853965 | TCCCTGATAGAAAAC[A/G]CCAGCCCTGTCCTTC | 93664 |
rs376212651 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122660638 | AACTTGGGCCAAGCG[C/G]TGTGGCTCACACCTG | 93664 |
rs376216179 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122467946 | TCCTTGACTCACTTT[C/T]TCTTTCTTCCTTTCT | 93664 |
rs376223248 | in-del | -/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122364739 | ACACTTATTGGGCTC[-/T]TTTTTTTTTTTTTGA | 93664 |
rs376224872 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122420555 | TCATAATTCTATTAG[A/G]TAACAAGGTTATCAA | 93664 |
rs376231152 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122514310 | GTTCAAACGAAATTT[-/T]ATATACAATTCTGAG | 93664 |
rs376246476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122708944 | ATATTTGGCCGTAGT[A/G]TAATTATTATCTTTG | 93664 |
rs376274796 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122810551 | AAGTCCTATTTAAAA[C/T]GTAGATTCCAGGAGC | 93664 |
rs376279707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122678001 | TCTTATACCACATCA[C/T]TGTATGTCTCTCTTG | 93664 |
rs376302097 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122779186 | AATTATCCAGTCTTG[G/T]GTATTTCCTCTTAGC | 93664 |
rs376309301 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122354242 | CTAGCATTTATTGTG[C/T]ACTAATTCCATTCTA | 93664 |
rs376315200 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122803677 | TTAAAAATTTATAGT[A/G]TTCTTTGATGGTAGT | 93664 |
rs376320877 | snp | C/T | 1.76911e-05 | 0.0029741 | intron-variant | CADPS2 | GRCh38.p7 | 7:122361025 | CAAACTATAATACAG[C/T]TATAGTGAGTATTTA | 93664 |
rs376322077 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122866048 | AAAGAATTTCTTCTG[C/G]GAATGTGACTGGGAA | 93664 |
rs376322343 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122474615 | CGTGACTCAAGCAGA[A/T]GACTACCTTTTATCA | 93664 |
rs376323191 | snp | C/G | 0.000163987 | 0.00905353 | intron-variant, missense | CADPS2 | GRCh38.p7 | 7:122393237 | CGAAGCAGTAGAAAT[C/G]TTAGGAATCTGTGGA | 93664 |
rs376325610 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122500328 | TTCTGTATTTTGGCA[C/T]GAAATTTATTTCAAT | 93664 |
rs376331464 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122867509 | TAGTCTTGTACAACA[C/T]ATACCCTGCCCAACT | 93664 |
rs376331657 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122498427 | CTGTTTAAATGTTGC[C/T]TCTGTCACATTTTTC | 93664 |
rs376339292 | multinucleotide-polymorphism | AC/GG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122718661 | GGGAACTGATCAAAT[AC/GG]GGCCGTGTTAAGGCT | 93664 |
rs376340609 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122706780 | AATGTATGTGTGTGT[C/G]TGTACATACATATAT | 93664 |
rs376347539 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | CADPS2 | GRCh38.p7 | 7:122738848 | TCCTATTGTACCCAG[C/G]GGGGGAAAAAAAAAA | 93664 |
rs376363533 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122837192 | TACTGGGTACATAAC[A/G]AAATGAAGGCAGAAA | 93664 |
rs376364788 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122718932 | CTTCTCTAGAACCTG[C/T]TGGATTTATGATAAT | 93664 |
rs376384484 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | CADPS2 | GRCh38.p7 | 7:122818969 | ACCCAATCTGCTCCC[A/G]ACATTAAATAAAACT | 93664 |
rs376387581 | snp | A/C | 0.00636936 | 0.0560724 | upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122888210 | AATAAGGAACCTGAG[A/C]GTTGAAGAATCCTTT | 93664 |
rs376389061 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122862509 | AGAAGGCCTCTCTCT[C/T]TCATGGCTATAGTTC | 93664 |
rs376393843 | in-del | -/AA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122705935 | TAATATATAATATAT[-/AA]TATATAATATAATAT | 93664 |
rs376397626 | snp | C/T | 8.32383e-05 | 0.00645075 | intron-variant, synonymous-codon | CADPS2 | GRCh38.p7 | 7:122393222 | TAAAGAAGGCATCCA[C/T]GAAGCAGTAGAAATG | 93664 |
rs376399491 | in-del | -/AT | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122541816 | TATATTTATATATTC[-/AT]ATATGTTTATATATT | 93664 |
rs376408356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122858006 | TTTATCGTGAAGAGC[A/G]AAAGAACAAAGCTTC | 93664 |
rs376408857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122537889 | AAAAAAGGATAAAAA[C/T]GCAAGAGAAGATTTT | 93664 |
rs376412349 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122577375 | ATTCTTGGCAAACTC[A/G]CAACTGTTGTCTACC | 93664 |
rs376419340 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122689701 | CCCAGGGGGTACAAA[C/G]TCCACTGGGGCCCAG | 93664 |
rs376420305 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122712437 | GAATATTTATCAAGA[C/G]CCTACTATGTGCATA | 93664 |
rs376434122 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122361224 | CTGGAAATAATACAC[-/T]TTTTTTTTTTTTTTT | 93664 |
rs376434868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122734738 | TTTATTTATTCATTC[A/G]AGAGTTTGTTGCATA | 93664 |
rs376437141 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122658429 | ATGCTGCTATAAAGA[G/T]ACAGGCACAGTATGT | 93664 |
rs376440849 | in-del | -/T | | | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122699442 | AACAAAATGGCAAGC[-/T]AAAAAAAAGGATAAT | 93664 |
rs376450164 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122483341 | TGCAAGCTAGAAGAA[-/A]GTGGAGCAACACCTT | 93664 |
rs376450985 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122541821 | TTTATATATTCATAT[A/G]TTTATATATTCATAT | 93664 |
rs376454425 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122369174 | TCTCGCTCTGTCGCC[C/T]AGGCTGGAGTGCAGT | 93664 |
rs376463521 | snp | A/C/G/T | 0.000149251 | 0.0086376 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122702123 | GTGTAAGTCTCCAGA[A/C/G/T]GCAATCTAAGTAAAA | 93664 |
rs376468377 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122334211 | GAGAATACACACACA[C/T]ACACACTCACTCACA | 93664 |
rs376470262 | snp | C/G | 2.28637e-05 | 0.00338102 | missense | CADPS2 | GRCh38.p7 | 7:122379389 | AACTAACAGTGAAAT[C/G]ATTTCTTTTACACTG | 93664 |
rs376474019 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122348825 | CTTTCATTTGGTGTA[C/T]GAAGGGTAATTATCT | 93664 |
rs376492617 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122641846 | TTGTGGCTCTCCAGG[A/G]GTTCATATGTTACGT | 93664 |
rs376501615 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122710480 | TAAGCTGAGCCACAT[C/G/T]GAGCCTCAGCTTTCT | 93664 |
rs376502675 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122770404 | TGGAAAACCTCACTT[C/T]AAAGAATACAGTGAG | 93664 |
rs376509948 | snp | G/T | 9.89642e-05 | 0.00703365 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698672 | GATTACATGCATTTT[G/T]GATTTTTCCCTCTGG | 93664 |
rs376518734 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122660909 | AGGAAGACTTCGTCT[C/T]GGAAAAAAAAGAAAA | 93664 |
rs376522444 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122835290 | CCCACCTGTACATCA[C/T]CATCATCAAAGACCA | 93664 |
rs376523760 | in-del | -/TA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122645515 | AAGTATATATATACT[-/TA]TATATATATAAGTAT | 93664 |
rs376531388 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122580571 | TTTCACACAGATTTA[C/T]CTAATGTTAATGCTT | 93664 |
rs376534119 | in-del | -/TCCCA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122860146 | ACCTCCCAACTTCCT[-/TCCCA]CCCAAGTTCACAAAA | 93664 |
rs376534855 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122576823 | TGTTGCCCAGTGGCG[C/T]GATCTCGGCTCATGA | 93664 |
rs376538305 | snp | A/G | 8.71555e-05 | 0.00660077 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122491331 | GTGGGGATCGGTATA[A/G]TCCACAGTATAGCCT | 93664 |
rs376557136 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122705409 | ACAGAGAATTGAAAT[A/C]TATTAGTAGAGATAA | 93664 |
rs376560816 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122802211 | GAAATATCCCCCTGA[A/T]TACCCTACAAATGCA | 93664 |
rs376568174 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122709906 | ACTCTGGGGACTGTT[A/G]TGGGGTTGGGGGAGA | 93664 |
rs376570359 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122388381 | AGGCAATAGTTGGGA[C/G]ACCTGAAAAAAAGTA | 93664 |
rs376573524 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122438877 | TCTTTTGAGCAATAT[A/T]TTTGAGAACAATAAC | 93664 |
rs376577722 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122444036 | AATTTTGATTAGTTT[A/G]TATGTCTAGAATTTT | 93664 |
rs376578607 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122416279 | AATAAGAAATACAAA[C/T]GAATACATTATTTAG | 93664 |
rs376580642 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122759164 | TTTTAGCAGCCATTG[C/T]CAAAATACTGTGGAG | 93664 |
rs376582905 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | CADPS2 | GRCh38.p7 | 7:122436432 | AACTCTACCCTTGTC[A/G]TTCATATAATGTAAA | 93664 |
rs376584932 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122454130 | AATAATTCTTCCCGA[C/T]AAGTGCAAATACTTT | 93664 |
rs376587645 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122705917 | TATAATATATTATAT[A/T]ATATAATATATAATA | 93664 |
rs376603909 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122374673 | TAAATGGGAGTTGAA[C/T]GAGAAAACATGGACA | 93664 |
rs376625299 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122830167 | GGTAGTCTGTCTCCA[A/G]GGTCTCTGGATCTTA | 93664 |
rs376627044 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122550202 | TAACTATTGTCTCTC[C/T]TTGCAACAAGAGATG | 93664 |
rs376644416 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122718809 | AATCATAAGCTGGTA[C/T]GGGATAACAGAGAAC | 93664 |
rs376647213 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122669088 | GTAATCCCAGCACTT[A/T]GGGAGGCCAAGGTAA | 93664 |
rs376650256 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122494097 | ATCGTCGATATGTGG[G/T]TGGGTCTCATATAAG | 93664 |
rs376655551 | in-del | -/A | 0.0596104 | 0.162024 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122537283 | AATGGTAATACAAGC[-/A]AAAAAAAAAACAAAC | 93664 |
rs376659412 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122471654 | GGCCTTATAAGCAGA[A/C]GCTGCATGAAAGTAT | 93664 |
rs376662464 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122616425 | TTAAAAGTGTTCTTC[C/T]TTTCAGCTCTGTTAC | 93664 |
rs376679282 | in-del | -/T | 0.398894 | 0.200825 | intron-variant | CADPS2 | GRCh38.p7 | 7:122332395 | ACTTTCTTCATCATC[-/T]TTTTTTTTTTTTTTT | 93664 |
rs376679409 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122843113 | TTAGCTTAGGATACC[A/G]AAGCTGGAAAAACAA | 93664 |
rs376679631 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122603407 | TCCTGGACTTAAAAA[C/T]AGGATGCTAAAAGAA | 93664 |
rs376690199 | snp | C/T | 0.161596 | 0.233848 | intron-variant | CADPS2 | GRCh38.p7 | 7:122645444 | ATATATGTATATATA[C/T]ACACACATATGTATA | 93664 |
rs376692762 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122585626 | TATTTTATGACAAAA[A/G]AATACATTATCTTGC | 93664 |
rs376698939 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122845043 | AATAAGGCTTCCTAG[A/T]CACTATTCCCTGCTG | 93664 |
rs376702325 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122786230 | GCAAATTAGCATCAT[C/T]GGGAAAATGGATGAG | 93664 |
rs376709011 | snp | A/C | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122541988 | TGTAATAGTAGCATA[A/C]AATCAAATCATCATT | 93664 |
rs376728409 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539777 | TCTCTGTCTCTCTCT[C/T]TCTGTTTCTCTCCAT | 93664 |
rs376738661 | snp | A/C | 1.83232e-05 | 0.00302676 | intron-variant | CADPS2 | GRCh38.p7 | 7:122360903 | ACAGTTAAAAGACCA[A/C]AGAAGAGAACTCATT | 93664 |
rs376760307 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122335348 | TCCACCTCCCGGGAT[C/T]AAGTGATTCTCCTGC | 93664 |
rs376769794 | snp | C/T | 0.0002143 | 0.0103491 | intron-variant, synonymous-codon | CADPS2, RNF133 | GRCh38.p7 | 7:122698247 | ATCTGTTGTTAATCG[C/T]TGCCATCTCCGGTTC | 93664 |
rs376771360 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122713475 | AGCACTACTTGGCTC[A/C]TACACAAACTGATGT | 93664 |
rs376787881 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122799738 | ATTAAAATGTTAACA[C/T]TGGCACTCATATTAG | 93664 |
rs376817060 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122477472 | AGTAAGCTGAGATTG[C/T]GCCACTGCACTCCAG | 93664 |
rs376818723 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122753770 | GTATACATATAAACA[C/T]ACGAACGCTTGCATG | 93664 |
rs376824526 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122608292 | CTAGTCTATAAGAGT[A/T]TCTGACTAATGAATT | 93664 |
rs376837128 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122673594 | AGACATAAAAGTTCT[A/C]CAAGTCCCCACCAGA | 93664 |
rs376841262 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122669546 | TGAAAGGCATGAGCT[C/T]CAGAAGGAAATGGGC | 93664 |
rs376843643 | in-del | -/AC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122774269 | GACATAGATAGATAT[-/AC]ACACACACACACACA | 93664 |
rs376848919 | snp | A/C/G | 6.29602e-05 | 0.00561042 | missense | CADPS2 | GRCh38.p7 | 7:122629277 | CTGCCAATTGCAGCC[A/C/G]GCCATCAAGTTCCCT | 93664 |
rs376850591 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122859946 | CAAACTTCATACCTC[C/T]GTATATCTCCAGTAA | 93664 |
rs376851859 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122568008 | CAGAATGGATAATAA[A/G]GACACAATTATATGT | 93664 |
rs376855150 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122744815 | TTGATCTCCCAGTCC[A/G]ATTCAAACCTCAGCA | 93664 |
rs376856192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122776510 | CCCAAAAATGTGGAA[A/G]TGACTTTGAAACTGA | 93664 |
rs376858296 | snp | C/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539737 | TAACTCTGCCTGTCT[C/G]TCCCTCTCTCTCTGT | 93664 |
rs376859181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122735564 | GGCCACATCATACTA[C/T]GCTTACTTTTAAAAA | 93664 |
rs376863135 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122716925 | TCCCTACTTGCAATG[G/T]GAACATGACTTTTTC | 93664 |
rs376864007 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122486249 | GTAATTCCTATGAGA[C/T]ATCTGGGAAAAGTAA | 93664 |
rs376865639 | in-del | -/ATAT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122645659 | ACATATATCTCTAAG[-/ATAT]ATATATATATATATA | 93664 |
rs376871762 | snp | A/G | 0.140581 | 0.224783 | intron-variant | CADPS2 | GRCh38.p7 | 7:122645473 | TATATGTGTATATAT[A/G]TATATATATTTAGCG | 93664 |
rs376878097 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122614896 | TGGTGATAAAATTTG[A/C]TTTCCTTAGAAATGA | 93664 |
rs376878865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122356743 | TTTACATATTTGCTC[A/G]CTCAAATTACTCTAG | 93664 |
rs376903037 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CADPS2 | GRCh38.p7 | 7:122601019 | CAATTTTTTAAATGT[A/G]GATAATGATAGGTTA | 93664 |
rs376909016 | in-del | -/AGA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122516088 | TTAGGGGTTAGTAGA[-/AGA]TGTTATAAGGAACAG | 93664 |
rs376933238 | snp | A/C/G | 1.66721e-05 | 0.00288717 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122438396 | CAAGGCAGCTTTCTC[A/C/G]AGACATTTTCTGACC | 93664 |
rs376945039 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122493466 | GTTAGAGACTGCTAA[A/G]TTGCATGACAAATTG | 93664 |
rs376972864 | in-del | -/ACA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122844886 | ATGTGGCTTAAAACA[-/ACA]TCAAAATGAAAAAAG | 93664 |
rs376983371 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122589877 | GTGTACTTAAACGTA[C/T]ATTTTAAAGGTTTGC | 93664 |
rs376991796 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122358618 | GTCTGTTTTCAGTTA[A/G]TTTTTGTGAAAGGTG | 93664 |
rs376998268 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | CADPS2 | GRCh38.p7 | 7:122480052 | TTGGAGAGAACAAAG[C/T]ACAGTTTAACCAAAG | 93664 |
rs377002793 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122667934 | GTGGGGGCCACGTGG[C/G/T]GGGAGGGAGGACTCT | 93664 |
rs377007290 | snp | C/T | 4.94539e-05 | 0.00497238 | intron-variant, synonymous-codon | CADPS2, RNF133 | GRCh38.p7 | 7:122698481 | AACGACATCTTCAAA[C/T]GCCTGATGAAACATG | 93664 |
rs377007409 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122354022 | TCCTTCATAAGCCAC[C/T]ATTTCCAGATCCCAT | 93664 |
rs377010700 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122803547 | GTGACAAAGCCATAA[A/T]TCACAGGAAACTTTC | 93664 |
rs377026929 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122408615 | TATTTTTAGGAGAAA[C/T]GGGGTTTTGCTATGT | 93664 |
rs377034930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122681598 | AAGCCCGCAAGGACC[A/G]AACACCCCCACCCAG | 93664 |
rs377043900 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122591066 | TGTTTGCAGATGACA[C/T]GATTGTATATTTAGA | 93664 |
rs377049939 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122659639 | ACTGACCCACAGATA[C/T]AGGAAGCTCAGAAAA | 93664 |
rs377053630 | in-del | -/ATAT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122579451 | ATAAAATTGCATCGA[-/ATAT]ATATATATATATATA | 93664 |
rs377072400 | snp | G/T | 1.6661e-05 | 0.00288621 | intron-variant | CADPS2 | GRCh38.p7 | 7:122345688 | TCCTGGTTTCTGTTG[G/T]GAAGGAAAAGCAGGG | 93664 |
rs377074253 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122571069 | AAGAGAATAACAGGA[C/T]AAGCCAAAGACTGAG | 93664 |
rs377076396 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122505637 | CAGATGGAAGAGTAA[A/T]AAAATACCAACAACT | 93664 |
rs377077869 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122783314 | TTAATATAATAACTA[C/T]TGTGGTTGATTTTAT | 93664 |
rs377085959 | in-del | -/AT | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122564811 | TTTAATTGCATAAAC[-/AT]ATGTGTGTACACAGA | 93664 |
rs377090910 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122735988 | TAAGATATTCTGAGA[A/C]AAGGTCCAGTTGGAC | 93664 |
rs377092660 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122849785 | CCCCAAGCCAGCCCC[-/C]AGCCCTCTCCCTTTA | 93664 |
rs377095346 | snp | A/G | 0.000333944 | 0.0129175 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122474474 | CTTGCAGGGGTTTGC[A/G]GAAATAAACTCATCC | 93664 |
rs377103969 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122886641 | AATTGCTCCGCCAGC[C/T]CCGGGCGCGCCGACC | 93664 |
rs377114701 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122361469 | AAACTCCTGACCTTG[C/T]GATCCACCCGCCTTG | 93664 |
rs377115606 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122854181 | CCTAGGTAACGTGGC[A/G]AAACCTGGTCTCCAC | 93664 |
rs377133942 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122559173 | TTCACTTGGAAGTCT[A/G]AAAGAACACCTAAGA | 93664 |
rs377136065 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817202 | TGTGACTCGGATGGG[A/G]GGACCTCCCTTGGGA | 93664 |
rs377144826 | snp | A/G | 1.84429e-05 | 0.00303663 | missense | CADPS2 | GRCh38.p7 | 7:122388724 | AAAAGGTCTTCTGAT[A/G]TTGCTGAGCCATTGC | 93664 |
rs377148125 | snp | G/T | 0.000342977 | 0.0130909 | intron-variant | CADPS2 | GRCh38.p7 | 7:122621431 | CAACAGAAATTATTG[G/T]GCATCATCATTTATG | 93664 |
rs377148931 | snp | C/T | 3.68141e-05 | 0.00429019 | intron-variant | CADPS2 | GRCh38.p7 | 7:122491275 | AGAATTCCATGCATA[C/T]ATACATGGCAGGAAA | 93664 |
rs377152096 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122692764 | AGCTGAAAGAACACT[-/C]GGGGCCGTAAGCAGG | 93664 |
rs377161208 | in-del | -/GAA | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122853786 | GTGACAGGAGAGATG[-/GAA]GAAGAGAGGGGAAGC | 93664 |
rs377162408 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122367034 | CTATTTTACTTTGCA[C/T]TCTCTCTCTGCTAAA | 93664 |
rs377169767 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122625880 | ATATCTACCTAGATA[C/T]TGGTCTAGATATATG | 93664 |
rs377175356 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122525642 | GCCTTCTGAAAAATG[A/C]ATCATGAGGCAATTT | 93664 |
rs377175580 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122662653 | CATTGGGTTACAGGC[G/T]TGAGCCACCATGCCT | 93664 |
rs377176905 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122414895 | GGTCATTTTTATTCT[C/T]GCTCATTTCATGTGC | 93664 |
rs377187148 | snp | A/C | 5.56158e-05 | 0.00527303 | intron-variant | CADPS2 | GRCh38.p7 | 7:122393170 | CCAGCTAACACACCA[A/C]CAGGAAATAAGTGAG | 93664 |
rs377196172 | snp | A/C | 0.118235 | 0.212457 | intron-variant | CADPS2 | GRCh38.p7 | 7:122680952 | TACTATGCAGCCATA[A/C]AAAATGATGAGTTCA | 93664 |
rs377198363 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122724656 | GAATAAACTCAAGTA[C/T]GGGAAGGTTACATAA | 93664 |
rs377206949 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122705555 | TATATTATATATATT[-/A]TATATTATATATTAT | 93664 |
rs377220056 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122470791 | GTAAGCCACCACACG[C/T]GGCATGATATGGACA | 93664 |
rs377221491 | in-del | -/GAA | 0.030665 | 0.119967 | intron-variant | CADPS2 | GRCh38.p7 | 7:122696516 | GACCCCATGGTCATG[-/GAA]GCAGTTATAGCTAAC | 93664 |
rs377223661 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122472725 | TTGTCCATGAAAAGA[C/T]AGAATAGGATTTTGA | 93664 |
rs377226252 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122385678 | ACTGTTGTGGAGGAG[G/T]GCAGAAGTCTCATGA | 93664 |
rs377238949 | snp | A/G | 3.31241e-05 | 0.00406952 | missense | CADPS2 | GRCh38.p7 | 7:122393483 | AAACCTCTGTGAATT[A/G]ACTGGGCGATGGAAG | 93664 |
rs377248325 | snp | C/T | 4.52919e-05 | 0.00475856 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554728 | TTTAAACGCATGATA[C/T]GGAGTGTCTATGGGT | 93664 |
rs377251944 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122440224 | TGCCACCTGTCAATG[C/G]AGGGCAGGAGGGCAT | 93664 |
rs377255824 | snp | C/T | | | intron-variant, upstream-variant-2KB | CADPS2, LOC105375481 | GRCh38.p7 | 7:122528873 | AATTTGATACTTTCT[C/T]GACAAGTTTGATATG | 93664 |
rs377260233 | snp | A/C | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122559008 | TGTCTCTTAGCTTAG[A/C]GAAAGGAAAAAAGAC | 93664 |
rs377263393 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122737771 | ATATTATACAAAATC[A/G]CCAGCTGTTCTAAAC | 93664 |
rs377263934 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122518820 | TAAGTATCTATCACA[C/T]AGCATGAGAGAAGCA | 93664 |
rs377270429 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122834972 | TTGAGAACTGAGAAC[A/G]GACAGACTGCCTCCT | 93664 |
rs377293044 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122445340 | CATGAGTACAGTATC[C/T]CTCCTTCTATTTAGG | 93664 |
rs377293435 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122834547 | CTAGCCAAGGAAAGC[A/C]GTGACAGACAGCACC | 93664 |
rs377296137 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122726800 | AAAAACTATCCACAT[A/G]TAAGATAGAGTTTGC | 93664 |
rs377300078 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122868173 | CTTCACTTGAGTGAC[C/T]GGCTCCTAAATCACC | 93664 |
rs377300513 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122638277 | CCAACATCCTGAGAG[C/T]CCAGGGATCTCACCC | 93664 |
rs377312547 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122519580 | TTGGGTTATTTCAAA[C/T]GGAGAGCACTATTTG | 93664 |
rs377317793 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122616854 | ATACAAAATGAAACC[A/G]GAAGCTGAGATAAAT | 93664 |
rs377321754 | snp | C/T | 5.26163e-05 | 0.00512888 | missense, upstream-variant-2KB, utr-variant-5-prime | CADPS2 | GRCh38.p7 | 7:122886093 | AGCTGCAGGCGGATC[C/T]TCCGCTCCTGCTCAT | 93664 |
rs377329543 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122695848 | GAAAAGGAGGAGAAA[A/G]AAGAAAAGGAAAAAT | 93664 |
rs377362229 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122851816 | AATTACCTCCCACTA[C/G]ATCCCTCCCACAACA | 93664 |
rs377367998 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122817952 | TTATTTCTGTGCCCC[A/G]ACCCTTTATTTCCGT | 93664 |
rs377374156 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122720960 | ATGTGCCAGGCGTTG[C/T]GTTAATTATGTTAAC | 93664 |
rs377390055 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122630913 | TATATAGGAGTTTCT[A/G]TGTCATCTCATAAAA | 93664 |
rs377391654 | snp | A/C/T | 4.97668e-05 | 0.00498812 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122701936 | TTGCAAGTTAAAATG[A/C/T]GTACTACATCTTGGG | 93664 |
rs377392074 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122710371 | GCATAGAGACATCAC[A/G]CTAGCAGAAACAGTG | 93664 |
rs377443514 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122884085 | GTATAAATCAACTCA[A/T]AGTAAATTTGCAAAA | 93664 |
rs377445478 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122415721 | TGCAAGCCCTCTTGT[C/G]GTCATTAACTTTCCC | 93664 |
rs377447594 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122627212 | CTCAATTTCCTCTTC[C/T]ATAAAATTGACTTCA | 93664 |
rs377449791 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122764256 | ATTCATATCCCTGTC[A/C]CAGAAGAGCACACAC | 93664 |
rs377454655 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122662470 | AACCTCCGCCTCCCA[A/G]GTTCAAGCAATTCTC | 93664 |
rs377455979 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122682468 | TCTATAAAGAAAATG[C/T]TTTTCTTGTTTTGCC | 93664 |
rs377461313 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122588076 | CGTAAATTTTTTTCT[G/T]GTAAATTTGAGTTCC | 93664 |
rs377462003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122367198 | ACAAGAAACTTTAAT[C/T]ACATAATCTAGGCAG | 93664 |
rs377465284 | snp | A/T | 0.000171985 | 0.00927163 | intron-variant | CADPS2 | GRCh38.p7 | 7:122491454 | GTTTACAGATTAGTC[A/T]CATTAAATTTACCAA | 93664 |
rs377468272 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122619674 | TGGAAAAAGTTATAC[C/T]ATAATTAAGGGACGA | 93664 |
rs377468609 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | CADPS2 | GRCh38.p7 | 7:122881654 | TTTGGACTATCATCA[C/G]ATCTGCTGGAAAACT | 93664 |
rs377471393 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122351443 | AAGCAGCCAGTTAAC[-/T]TTTTTTTTTGTTAAA | 93664 |
rs377476434 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122503063 | TTGAGACGGGGTCTC[A/G]CTCTGTCGCCCAGGC | 93664 |
rs377480602 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122371819 | GGGACACTAGGATGA[C/T]GAGATTTTACAATGG | 93664 |
rs377486391 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122466365 | ACTTATCCTGGATGA[C/T]GGGGTTCTAGGCTCC | 93664 |
rs377488308 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122754337 | CAAAGTGTGACTCTT[A/G]AAGGAATTTGATAAA | 93664 |
rs377488472 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122692910 | AGCTTAACTCTCTCT[C/G]TCTGGGCACAAGTGT | 93664 |
rs377488845 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122413937 | ACATTCAAAGAAAAA[C/G]AGACATTCTGTAATT | 93664 |
rs377489463 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122434054 | AAAGCCACGAACAAC[C/G]CTGAACTTCTTGTTT | 93664 |
rs377491340 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122779288 | ACACTTTAGGTGGGA[A/C]AGCTCTACTTCAGGC | 93664 |
rs377494428 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122410200 | AATACAAAAATTAGC[C/T]GGCGGTGGTGGTGTG | 93664 |
rs377506422 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122651985 | CTGCTCATACTCCAG[G/T]AGTCAACGATGTGAA | 93664 |
rs377509432 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122569430 | GTGGATAGGAAGAAT[A/C]AATACCGTGAAAATG | 93664 |
rs377513180 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122609139 | TCTATCTTCACCTTC[C/T]ATAGGGTATTACTAG | 93664 |
rs377515214 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122630139 | TTTCTCCTTTTGCAC[G/T]CTCATCACGAAGAAG | 93664 |
rs377517378 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122610796 | ATTAGTAGAGTAGAA[A/T]TAATAAAATAATCTA | 93664 |
rs377524580 | snp | G/T | 6.63372e-05 | 0.00575884 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122474393 | CACCAAGCAAGAATA[G/T]GAATCATTCAGTCTG | 93664 |
rs377529560 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122819478 | ATGGAAGGTAAGCCC[C/G]GTCCCCTTCTTAATC | 93664 |
rs377531054 | in-del | -/CAA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122581057 | GCTTGTGGGAAATAA[-/CAA]ATTATTTTATGTAAT | 93664 |
rs377551249 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122377906 | TTTCCACTCTAAGAC[A/G]TGCCATGAGATAATT | 93664 |
rs377555188 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122617030 | AGAGCATTGCTTCAT[A/G]TTTCAGAATATTATT | 93664 |
rs377555868 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122672697 | TGCACCTTTGGCAGC[A/C]AGATGTCCTGCTGGT | 93664 |
rs377560103 | in-del | -/A | 0.0973687 | 0.197999 | intron-variant | CADPS2 | GRCh38.p7 | 7:122501901 | AAAAAAAAAAAAAGG[-/A]AAAAAAAAGTCACCT | 93664 |
rs377566915 | snp | A/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122538141 | TCCCACTTATACAAA[A/T]TCAGTAAAAAAAAAA | 93664 |
rs377569810 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122636007 | TTACACGTGAGATGC[C/G]TCTCTTGAAGACAAC | 93664 |
rs377572952 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122606599 | ATGAGGACTGGACTT[A/T]CTACCAATCTGGGCA | 93664 |
rs377574360 | snp | A/C | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122537132 | ATGACAAAAGTTTAC[A/C]TATGTAACAAACCTA | 93664 |
rs377578010 | snp | C/G/T | 3.55475e-05 | 0.00421577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122438501 | GGGTGAGGGGCAGGG[C/G/T]TGGGGATAGACAGAT | 93664 |
rs377578834 | snp | A/G | 1.74912e-05 | 0.00295725 | intron-variant | CADPS2 | GRCh38.p7 | 7:122320387 | TTAGATTATATGCGT[A/G]TACATAGATATATAC | 93664 |
rs377579773 | snp | C/G | 0.00014284 | 0.00844983 | missense | CADPS2 | GRCh38.p7 | 7:122663241 | AGACCACTTACCTGA[C/G]ATGCATTATAAAGGA | 93664 |
rs377581158 | in-del | -/AAGT | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122646257 | AACAATAGGAAACAC[-/AAGT]AACATTACTGTACAT | 93664 |
rs377583045 | snp | C/T | 1.6804e-05 | 0.00289858 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122702629 | AATGTTATATTCAGG[C/T]GAGCTGTCCAAATGG | 93664 |
rs377589504 | snp | A/C | | | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122699973 | TTTTGCAGAACTTAA[A/C]AAATATCCCTATTAG | 93664 |
rs377600435 | snp | A/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122562970 | CTAACAAAGTTCAAG[A/T]TCCACACAACCTAAC | 93664 |
rs377604588 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122775985 | AAAAATTTTTTTCTA[A/G]AGAAGTTAGATGGGC | 93664 |
rs377605925 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122487306 | TTGAGCCACTGCGCC[A/G]GCCAAACATAACTTT | 93664 |
rs377607152 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122822573 | CCTCTGAGCCCAAGC[C/T]AAGCCATCGCATCCC | 93664 |
rs377613852 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122439864 | ATTATACTTCCCATG[C/G]CAACAAACTTTACAT | 93664 |
rs377619061 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122349275 | GCTATATTTAGAAAT[A/C]TCTTCTAAATTGGTA | 93664 |
rs377620531 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122854321 | GGCTGTAGTGAGCCA[C/T]GATCATGCCGCTGCG | 93664 |
rs377636025 | snp | A/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122538144 | CACTTATACAAATTC[A/T]GTAAAAAAAAAAAGA | 93664 |
rs377642170 | snp | A/G | 1.64863e-05 | 0.00287104 | intron-variant, missense | CADPS2, RNF133 | GRCh38.p7 | 7:122698299 | CTATGAATGTGATAA[A/G]AGATGAAATATGCTA | 93664 |
rs377647832 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122875703 | TAAATATGTAAATAC[C/T]GGTTCAAGGAAAAAA | 93664 |
rs377649910 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122852070 | GAATCCAGAAGTCTT[C/T]ACTGACTCAAAAATT | 93664 |
rs377650095 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122676961 | TTCTAGCCTTCTCTT[A/C]CATTTCTTTCAAGAA | 93664 |
rs377650885 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122344713 | ATCCATTAGAACATG[A/G]TTCTGTTTATGGAAT | 93664 |
rs377660940 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122462252 | CTGGAGGGTAATATT[C/T]TAAGGACTCTGAACT | 93664 |
rs377682494 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122333886 | ATATTTATAAATATA[A/T]ATTTATATATATATA | 93664 |
rs377686883 | snp | A/C | 4.19498e-05 | 0.00457965 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554707 | GTATGGAAAAAAAAA[A/C]CCACATTTAAACGCA | 93664 |
rs377711901 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122828616 | TATTGTATGTACTCA[C/T]ATTTAAGTTATCTGT | 93664 |
rs377713898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122875325 | GTAAGTGGATCAAAC[A/G]AAGTTAATTTTCAGT | 93664 |
rs377715457 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122390009 | TGAAAAGCTTATTCC[-/T]GCCCTCCACCCTGGC | 93664 |
rs377715881 | snp | A/G | 6.62932e-05 | 0.00575693 | synonymous-codon | CADPS2 | GRCh38.p7 | 7:122663357 | ACTTAGGGCCATTCT[A/G]TTTGGCTGTTTGCAC | 93664 |
rs377719800 | snp | C/T | 9.13467e-05 | 0.00675759 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122702669 | TTGAGTCAGGAAAGC[C/T]AAGTAGTAGAAAGAT | 93664 |
rs377724213 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122362463 | ATTAGTCTCAAAAGT[A/G]GTTTACATTTCTAAA | 93664 |
rs377724931 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122343745 | ATAATGGGAATAACA[C/T]CAACTCAATTTCCCT | 93664 |
rs377738414 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122345918 | TAGATCCGTAGATAT[C/T]TTTTTTTTTTTTTTG | 93664 |
rs377739349 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122512572 | GTTCAGAATCCAATC[A/G]TAAGCAAATACACAC | 93664 |
rs377752358 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122419204 | ATGGGAGGAAAAGAA[C/T]GTTAAAAAATTCAAT | 93664 |
rs377766974 | in-del | -/CA | 0.0685596 | 0.171987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122625783 | CTCTCCCTGCCCTCC[-/CA]CACACACACACACAT | 93664 |
rs386360115 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122672583 | TGGCTTGAGGTCACA[-/A]CACCTCCTGGGAGAA | 93664 |
rs386411171 | in-del | -/TTTTT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122345928 | ATATCTTTTTTTTTT[-/TTTTT]TTTTGTTAAATGGCT | 93664 |
rs386411172 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122364733 | TCCATCTCAAAAAAA[-/A]AAAAAAGAGCCCAAT | 93664 |
rs386411173 | in-del | -/GTGT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122426456 | TAAAATATAAATGTG[-/GTGT]TGTCTTTTAAAAAGC | 93664 |
rs386411174 | in-del | -/CTTC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122511277 | AAGTTTTACAATTCC[-/CTTC]TTCATTTCCAAACTC | 93664 |
rs386717353 | multinucleotide-polymorphism | AG/CA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122322899 | GGACAAGACTACTAA[AG/CA]GCAAGTAGTTTGGGT | 93664 |
rs386717354 | multinucleotide-polymorphism | CT/TA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122356506 | CCCCATCTTCCTTTG[CT/TA]TATTGTACTCTTCGG | 93664 |
rs386717355 | in-del | CCCCG/TCCCCC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122369127 | AGAAGAATTTTTGTT[CCCCG/TCCCCC]CCCCCCCCCCTTTTT | 93664 |
rs386717356 | multinucleotide-polymorphism | CGT/TGC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122369217 | GCTCACTGCAAGCTC[CGT/TGC]CTCCCGGGTTCACGC | 93664 |
rs386717357 | multinucleotide-polymorphism | CAA/GTT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122475176 | CTGTAGACCCTGCGG[CAA/GTT]TATCAAAAGGCAAGC | 93664 |
rs386717358 | multinucleotide-polymorphism | AAC/TAA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122485871 | AAGCCAATGTTTATT[AAC/TAA]CATTTTGAAAATCCC | 93664 |
rs386717359 | multinucleotide-polymorphism | CT/TC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122492702 | TTAGTGTATTTTTTT[CT/TC]TTTTTTTCTTTTTTG | 93664 |
rs386717360 | in-del | CCCTG/GTC | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539761 | TCTCTGTCTCTCTCT[CCCTG/GTC]TCTGTCTCTCTCTTT | 93664 |
rs386717361 | multinucleotide-polymorphism | AT/GA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122665002 | TGGGGTCTCATTTAT[AT/GA]GACTCAGGCTGGTCT | 93664 |
rs386717362 | in-del | GTG/TT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122672846 | CTGTGTCCGGAATTG[GTG/TT]GGTTCTTTGTCTTGC | 93664 |
rs386717363 | multinucleotide-polymorphism | GC/TT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122674099 | TACTTCCCGGGGCCA[GC/TT]GGTGCTGGCTGGCCG | 93664 |
rs386717364 | in-del | ACCCCATGGTCATGGAA/GGGTG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122696502 | CTTTAGTCTTCCATG[ACCCCATGGTCATGGAA/GGGTG]GCAGTTATAGCTAAC | 93664 |
rs386717365 | multinucleotide-polymorphism | AT/TC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122707579 | TAATATCATGAGAGC[AT/TC]TCTAGGAATTCAAAA | 93664 |
rs386717366 | in-del | CAA/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122719016 | TGCCATAAATGTACA[CAA/G]TTTTGAGGAAGTGAG | 93664 |
rs386717367 | multinucleotide-polymorphism | AG/CA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122795743 | CTATGACATACCCAC[AG/CA]CAAACATCATACTGA | 93664 |
rs386717368 | in-del | CAG/TAAA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122801064 | AAACACTATTTGGGC[CAG/TAAA]GAGAAAATTAAAATG | 93664 |
rs386717369 | in-del | AA/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122801066 | ACACTATTTGGGCTA[AA/G]GAGAAAATTAAAATG | 93664 |
rs386717370 | in-del | C/GTGTTGTTA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122808242 | TATTAATGGTGCAGT[C/GTGTTGTTA]AACTGCTTCCCTGGC | 93664 |
rs386717371 | multinucleotide-polymorphism | CATACAC/TATACAT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122809118 | ATGTGGTTTTCTGTA[CATACAC/TATACAT]TGTATAAATATTGTT | 93664 |
rs386717372 | multinucleotide-polymorphism | AGA/TGC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122830346 | TCCATTCATTGACAC[AGA/TGC]AACAAATACAGCATA | 93664 |
rs386717373 | multinucleotide-polymorphism | CA/TG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122860191 | CAAAGGTTGGAAGGA[CA/TG]TGCTCCTATCTCTAG | 93664 |
rs397686472 | in-del | -/GAA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122678876 | GAAACCATGGCAGAA[-/GAA]CATAAATTGTGAAGA | 93664 |
rs397687230 | in-del | -/AT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122756235 | AATTAATATATATAT[-/AT]TGGTATGTACCAAGT | 93664 |
rs397732537 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122738871 | AAAAAAAAAAAAAAA[-/A]CTTTTGCCATGGGCA | 93664 |
rs397757928 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122724747 | TTCACCTTTTTTTTT[-/T]CCCATGTGTTTAAAT | 93664 |
rs397766237 | in-del | -/ACA | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122782368 | CTCATTACTGAAACA[-/ACA]CCAGTAGCAAATCTT | 93664 |
rs397768266 | in-del | -/T | 0.375 | 0.216506 | intron-variant | CADPS2 | GRCh38.p7 | 7:122630390 | AGGAACATCTTCCTC[-/T]TTTTTTTTTTTTGAC | 93664 |
rs397774230 | in-del | -/A | 0.375 | 0.216506 | intron-variant | CADPS2 | GRCh38.p7 | 7:122503049 | GCGAGACCCCGTCTC[-/A]AAAAAAAAAAAAAAA | 93664 |
rs397782659 | in-del | -/C | 0.375 | 0.216506 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122538675 | CTTACAGTGTACTTT[-/C]CTATCTCCTTACCCA | 93664 |
rs397782805 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122435000 | AGCCTCAGGTTTTTT[-/T]GCTTTAAATTTGTAT | 93664 |
rs397788828 | in-del | -/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122799235 | TGTATCTGTGTTCTG[-/T]TTTTTTCTGGCATTA | 93664 |
rs397791285 | in-del | -/A | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122848917 | TACTAAGAAAAAAAA[-/A]TGCTCCTGAAGTATT | 93664 |
rs397792836 | in-del | -/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122757920 | CTCTGTTGATGTTAG[-/T]TTTTTTTTTCCCTGT | 93664 |
rs397795779 | in-del | -/TCTT | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122546553 | ACCTCTGCTGATCTT[-/TCTT]AAGCTTTTTCCTTCC | 93664 |
rs397809336 | in-del | -/A | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122847608 | GTTAATGATGACAAG[-/A]AAAAAAAAAAATCTA | 93664 |
rs397820389 | in-del | -/AA | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122443735 | AAAAAAAAAAAAAAA[-/AA]TGCTGTCAACTTTTA | 93664 |
rs397826041 | in-del | -/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122349093 | TGTGGGGTTTTTTTT[-/T]GGTGTGTACATGAAG | 93664 |
rs397830586 | in-del | -/TC | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122666050 | CTCATCTAATCACTC[-/TC]ATTGAGCAGTGACAT | 93664 |
rs397838210 | in-del | -/TG | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122410728 | GTAATTACAAATATG[-/TG]TTGACTACCGCAATC | 93664 |
rs397888941 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122340856 | GATGCCTTATGTGTT[-/A]AAAAAAAAAAAAAAA | 93664 |
rs397889801 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122669367 | TATATTTTTTTTTTT[-/T]GAGAAAAAGTAATTA | 93664 |
rs397935658 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122809430 | AAAAGAAAAAAAAAA[-/A]TTTAGGCAGGCATGG | 93664 |
rs397939976 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122611325 | TGGGCTAAGAAAAAA[-/A]GAAAGGCTATTCAAA | 93664 |
rs397947462 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122454338 | GTTAGGTTAATTCCC[-/C]AAGGTCACACCGCTG | 93664 |
rs397950814 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122796041 | TCAATGAGAAAAAAA[-/A]TCACTAACATTCCTA | 93664 |
rs397951095 | in-del | -/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122878031 | GGGAGGCCGAGGCGG[-/G]TGGATCATGAGGTCA | 93664 |
rs397953383 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122410459 | TTTTTTTTTTTTTTT[-/T]GTAGTAAATATAGTT | 93664 |
rs397965856 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122472315 | TGTAAGAGAAATAAA[-/A]GAATAATGAGAAAAA | 93664 |
rs397965981 | in-del | -/TA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122684449 | GCATATATATATATA[-/TA]CACACATATATATAC | 93664 |
rs397968798 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122882634 | TTTTTTTTTTTTTTT[-/T]ACTTTCTCCTCCGAG | 93664 |
rs397970454 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122828254 | TTTCTACTATTTTTT[-/T]ATCATTTACATGGTA | 93664 |
rs397973243 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122474063 | AGAGGTTTTAAAAAA[-/A]TCTTTATTTAAAGCC | 93664 |
rs397973386 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122631704 | TTTTCTTTTTTTTTT[-/T]AATTTCAGATTTGGA | 93664 |
rs398006074 | in-del | -/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122326091 | TGTTTAAGTTGTAGA[-/T]TTTTTTTTTTTTTTT | 93664 |
rs398006075 | in-del | -/GTGTGGGT/GTGTGTGT | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122328160 | AAGGTGTGTGCGTGC[-/GTGTGGGT/GTGTGTGT]GTGTGTGTGTGTGTG | 93664 |
rs398006076 | in-del | -/AAAAA | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122345932 | AGATAGCCATTTAAC[-/AAAAA]AAAAAAAAAAAAAAG | 93664 |
rs398006078 | in-del | -/A | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122463337 | GCGAGACTCCACCTC[-/A]AAAAAAAAAAAATCT | 93664 |
rs398006079 | in-del | -/A | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122484679 | AATAGTGACTTTCAG[-/A]AAAAAAAAAAAAGAA | 93664 |
rs398006081 | in-del | -/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122525152 | AAACTTTTTAAAGAA[-/T]TTTTTTTTTTTTGAG | 93664 |
rs398006083 | in-del | -/A | 0 | 0 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122547084 | ATAAAAATTAAAGGC[-/A]AAAAAAAAAACACCC | 93664 |
rs398006084 | in-del | -/TT | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122580467 | GAATTTTTTAATGGG[-/TT]TTTTTTTTTTTTTTT | 93664 |
rs398006085 | in-del | -/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122602207 | ATGAAAAAAATAAAC[-/T]TTTTTTTTTTCCTTA | 93664 |
rs398006086 | in-del | -/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122610163 | AAGCCCCCAGTGCTC[-/T]TTTTTTTTTTTTATT | 93664 |
rs398006087 | in-del | -/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122683755 | CTGGGAATCTGTTTG[-/T]TTTTTTTTTTCTTCA | 93664 |
rs398006088 | in-del | -/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122713316 | GTTGTAGAGCTAGTG[-/T]TAAGTACAGGATTTA | 93664 |
rs398006090 | in-del | -/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122731683 | TTGTTAATTGAAGGG[-/T]TTTTTTTTCCCCTCT | 93664 |
rs398006092 | in-del | -/TG | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122747844 | GCAGAGGAAGCAAAC[-/TG]TGTGCAAAGGCACAA | 93664 |
rs398006093 | in-del | -/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122840568 | ATTTGATGGCTTTTC[-/T]TTTTTTTTTTTTTTG | 93664 |
rs398040103 | in-del | -/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122759014 | TTTAAGGACCTTTAA[-/T]TTTTTTTTTTTTTCC | 93664 |
rs398040104 | in-del | -/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122405670 | TAAGCCGGTTTTTTG[-/T]TTTGTTTTGTTTGAG | 93664 |
rs398047559 | snp | C/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122366642 | ACACACACACACACA[C/T]ATATATATACATACA | 93664 |
rs398048049 | in-del | -/AAAAAAAA | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122351403 | AAAAAAAAAAAAAAA[-/AAAAAAAA]TTCCAAACTATTATT | 93664 |
rs398048050 | in-del | -/T | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122429891 | TGCAGTTTTTTTTTT[-/T]AATAAACACGTGGCC | 93664 |
rs398048051 | in-del | -/A | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122438943 | TCTGAAAAAAAAAAA[-/A]TCAAGACCTCTAATC | 93664 |
rs398048052 | in-del | -/A | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122595173 | ACCAAAAAAAAAAAA[-/A]TCCTTTCAAATGTAA | 93664 |
rs398048054 | in-del | -/A | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122684661 | AAATACCTCAAAAAA[-/A]CCTTTCACTTGAGAA | 93664 |
rs398048055 | in-del | -/A | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122749976 | AAAAAAAAAAAAAAA[-/A]GAAAAAGAGAGAGTA | 93664 |
rs398048056 | in-del | -/A | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122809595 | AAAAAAAAAAAAAAA[-/A]GACTGCCTCATACTA | 93664 |
rs398048057 | in-del | -/A | 0.5 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122830408 | GCTAAAAAAAAAAAA[-/A]TCAAAGGATGCAAAT | 93664 |
rs398067232 | in-del | -/AA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122710064 | TAAAAAAAAAAAAAA[-/AA]TGACCTTCTGCCAAC | 93664 |
rs398067233 | in-del | -/AGT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122764597 | TGAAGCAAAATAAGT[-/AGT]CAGGGTATAGCAACA | 93664 |
rs398086128 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122527429 | GCTAAAAAAAAAAAA[-/A]ACACAAAACTGTCTG | 93664 |
rs398086129 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122715720 | GCAAAGAAAAAAAAA[-/A]AGCCAATTGTACAAG | 93664 |
rs398086130 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122724746 | TTTCACCTTTTTTTT[-/T]TCCCATGTGTTTAAA | 93664 |
rs398111801 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122322039 | GAACCAGTGAGATAA[-/A]TTCTGAAAGGTATGT | 93664 |
rs398111804 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122367385 | AAATCCTTTTTTTTT[-/T]GGCAATAATTGAGAA | 93664 |
rs398111805 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122452084 | CTGTGAAATCAATGT[-/T]GAGTTTCATCAGAAT | 93664 |
rs398111806 | in-del | -/A/C | 4.14951e-05 | 0.00455476 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554706 | GTATGGAAAAAAAAA[-/A/C]CCCACATTTAAACGC | 93664 |
rs398111807 | in-del | -/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122658371 | AAATACCATTCGACC[-/C]AGCCATCCCATTACT | 93664 |
rs398111808 | in-del | -/T | | | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122704543 | TTTTGCAGATTTTTT[-/T]GTGGGTGAAGTGTTT | 93664 |
rs527237270 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122502615 | AAATCTAGAGGTTAG[G/T]ATTCACATTTTGTAA | 93664 |
rs527244881 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122584721 | ACACTTTAACTACAG[C/T]ACCCCATAAATTTAG | 93664 |
rs527247392 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122668312 | GTGGAAGCCCATGTG[C/T]GTGCATTTGTATATG | 93664 |
rs527265472 | in-del | -/TA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122676490 | TTATATACCAGGCTG[-/TA]TATCTCGACTGCTCA | 93664 |
rs527267850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122844309 | GTAATCACGCCCTTT[C/T]ATAGTTTTAAAGTTA | 93664 |
rs527275439 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122751053 | AACCGATTTTTAAAT[C/T]AGGCTTTCACTCATG | 93664 |
rs527279877 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122324124 | TCTCCATTGACATGT[A/G]ATGTGTAGCTATAGT | 93664 |
rs527296416 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122668836 | TGAGAGGAAGCCCTG[A/T]CTTCCCCACCACCAC | 93664 |
rs527300319 | snp | G/T | 6.68349e-05 | 0.0057804 | intron-variant | CADPS2 | GRCh38.p7 | 7:122490300 | TGGAGGAAACAAAAA[G/T]ACATCATTAAAAATT | 93664 |
rs527308272 | snp | C/T | 0 | 0 | intron-variant | CADPS2 | GRCh38.p7 | 7:122661761 | TTGGATTCCCTAATA[C/T]CTACAGAGGTTTTGG | 93664 |
rs527309660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122326351 | AAACTGAAATTCTTC[C/T]TTAATGCAATTTTCT | 93664 |
rs527315220 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122332157 | AATCCAATAACGTAA[A/T]ATACAATGTAAATAA | 93664 |
rs527317296 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122751205 | GCTGTTCTCAAACTC[C/T]TGAGCTCAAGGGTTC | 93664 |
rs527324595 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122799840 | CAATGTCTCATATTC[A/G]TACTTCTTTCAGTCA | 93664 |
rs527336933 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122630107 | GTTAAGTGTTAATTT[A/T]CTCTTGACTTTAGTT | 93664 |
rs527349219 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122860394 | ACCACACCTGGCTAA[A/T]TTTTTTACTTTTTAT | 93664 |
rs527351475 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122400282 | CTCTACCAAAAATAC[A/T]AAAAATTAGCTGGGT | 93664 |
rs527353515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122392348 | AGGATATGCCAATAG[C/T]ACTAATAATTTACTG | 93664 |
rs527354070 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122700072 | ATCAAAGCTAAAGGA[C/T]GGCATGTGGACTCAC | 93664 |
rs527358030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122766799 | AGATAAGGAGTGACA[A/G]GTAACTGTCACTCTG | 93664 |
rs527359516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122637312 | GATCCTCTTACCTCA[A/G]CCTCCCAAGTAGTTG | 93664 |
rs527360395 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122673682 | TGCTGATTGTTGCAT[A/T]TACAATCCTCCAGCT | 93664 |
rs527369517 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122341142 | CATATTGCAACTTTT[A/T]AAAAAAATTTGGGTT | 93664 |
rs527371214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122591160 | ATACAAAATCAATGT[A/G]CAAAAATCACAAGCA | 93664 |
rs527376677 | snp | A/C | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122537555 | GAGTAATAAAATAAA[A/C]CAAATAAAAACAAAA | 93664 |
rs527377470 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122444768 | TTTTATTCTAACAAT[A/G]TCTTTGGAAGATCGA | 93664 |
rs527383791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122544078 | CAGTTCCACTCCTAC[A/G]TGTCCACTCAAGAGA | 93664 |
rs527384315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122348682 | GGGAATTTCACACCT[A/G]GTGAATACATTTTCA | 93664 |
rs527398892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122813773 | ATAAAAGACAGTGGA[C/T]ATTGGAAAATACTTA | 93664 |
rs527410985 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122591606 | ACAAGGCTACAGTAA[A/C]CAAAACAGCATGGTG | 93664 |
rs527411892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122852502 | ATGTGGGTGGGGCAG[A/G]GTGTGGTAGCAACTT | 93664 |
rs527417125 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122451794 | TACCAAACATTTGAC[A/C]AACTAAGTGAAATCC | 93664 |
rs527417168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122443934 | TTAAGTTTTGACATA[C/T]GCATATACTTGTGAC | 93664 |
rs527425585 | in-del | -/AT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122366646 | CACACACACACACAC[-/AT]ATATATATACATACA | 93664 |
rs527428012 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122851918 | TTACTGTATAGACTA[C/T]TTAAAGCATCTTTCA | 93664 |
rs527429642 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122758823 | AGTGATAGCTGCAAA[C/T]CATTAACGTTTTTAA | 93664 |
rs527433031 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122604280 | TTCACTCACAGATTG[C/T]TGAAGATCTTGACAA | 93664 |
rs527436622 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122674038 | CTGGCAGTACTGGGG[G/T]ATCCGGCACACCCTC | 93664 |
rs527446811 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122597185 | CATGAGGCTTGGGGG[C/G]TCAAATATCCAAACT | 93664 |
rs527448612 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122679526 | GTGATCTCGCCCTAA[A/C]CTTGTGATCTCACCC | 93664 |
rs527452721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122686826 | AGTAGCTGGTATTAC[A/G]GGAATGTGTCACTAC | 93664 |
rs527463689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122399588 | AGTTAATGTCCCACA[A/G]TACTTGCCCCATCAA | 93664 |
rs527472625 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122818419 | GTCTGAGGTGCCTGA[A/C]GTCCAGGCATTCTTT | 93664 |
rs527473294 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122556878 | TAGCTCTGATAATAT[A/C]ACTTCTTCCTATTGC | 93664 |
rs527478177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122727977 | CTATGAATGTGTTGA[C/T]ATTTTTTATCTCCTC | 93664 |
rs527478742 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122648833 | GCAGCCTAAGAACTT[A/C]ATAGGCAACACAGAG | 93664 |
rs527482300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122505066 | GTCTTTTAAAAATTA[C/T]TGCTTTCTTAAAAAC | 93664 |
rs527483901 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122825910 | CGTAGAATTCTGCTC[C/T]GGAGAGAATTTCAAA | 93664 |
rs527489128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122717964 | TATAGGTGCATTCCA[C/T]CACACTCGGCTAATT | 93664 |
rs527490438 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CADPS2 | GRCh38.p7 | 7:122722928 | AAAACAAGCAATGGG[G/T]AAACGATTCCCTATT | 93664 |
rs527493151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122643341 | AAAGATAGAGCATAG[C/T]TCTACCCAACTGACT | 93664 |
rs527493779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122642538 | ATAACTACTAAGTTT[C/T]ACCCAACAGCTTTTT | 93664 |
rs527494705 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122636874 | AATTCTCTGTATTTC[C/T]TAAATTTGTACGTCC | 93664 |
rs527495908 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122868561 | ACAAAGAGCTTAGAA[A/T]ATAGAATCCCTGATT | 93664 |
rs527507666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122774572 | ACCAATTATGGTTTG[C/T]CCAATTACCATAATC | 93664 |
rs527509729 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122557331 | GGGAGTTCTTTTCAG[A/G]ACACACAATACAGCT | 93664 |
rs527521816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122406193 | TTTTATCACAGACTC[A/G]AAGAGGTGAACAACC | 93664 |
rs527522810 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122818754 | CAATTTACTCTTAAA[A/C]AGGTGGCTGGAGCTA | 93664 |
rs527535275 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122329805 | GCCTTTAGACCCTCC[A/G]AGGCTGATATTCCTA | 93664 |
rs527535425 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122563010 | TTATTTCTGCTATTT[C/G]AAAGCCTTTCTTGAA | 93664 |
rs527545693 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122459155 | TGATTCATAATTTGA[C/T]TGTTTTAACGAACTG | 93664 |
rs527547114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122832462 | CCTAAGTTAATCTTA[C/T]GCAGCCATCTCTGTC | 93664 |
rs527553369 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122413643 | TGGAGCAAAGGAACT[A/C]TAGCTTGAACATCCA | 93664 |
rs527555717 | snp | A/G | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122531382 | CCAGCCTCACAGTCT[A/G]GTCATCTACACCTGC | 93664 |
rs527556679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122513369 | AATAATGTTGTGCTT[C/T]CATGTAATCACATTT | 93664 |
rs527563921 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122602968 | TGCCAACATGGAAGA[C/T]ATGGCTGCAAAATTA | 93664 |
rs527565071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122883578 | TTTTGGCATTACTTA[C/T]TAGCTTGTGCATCAA | 93664 |
rs527566793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122362754 | TCAACAAAGTGATAA[C/T]AGTTCTAGGGACACA | 93664 |
rs527567401 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122354784 | CTCTTTTTTCAAATG[G/T]CTGTTGTCTTTGCCA | 93664 |
rs527578684 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122779657 | ACAAACTTTGTTTCC[C/T]CCCTTTCTAATAGTA | 93664 |
rs527580556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122832940 | TCACTTTTGTTTCCC[C/T]TCCCAGATTATGTGA | 93664 |
rs527582928 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122499281 | CCACTTTAAGAATAC[C/T]TCATGGTACATCTTC | 93664 |
rs527583640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122794019 | TCTGACGGGCTTCTC[C/T]TTGTAGGCGTCCTGA | 93664 |
rs527588517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122512397 | ATACTCTTTTCATAT[A/G]TTGGGAACAAAATAG | 93664 |
rs527591648 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122420528 | GGCCAAGAAGTTTAA[G/T]GCATTCTACAGTCAT | 93664 |
rs527595060 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | CADPS2 | GRCh38.p7 | 7:122500743 | CAATAACTTAGGAAA[C/T]AACTAATTAGGGAGT | 93664 |
rs527598666 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122535092 | CATGACTTTTAACCT[-/A]ATCACTTTACACAAG | 93664 |
rs527600381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122412999 | ACTTAAATTGCAAAA[C/T]AGCAATGTGGTTTAT | 93664 |
rs527604221 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122603575 | ACCCCAATTAACTCA[C/G]AAAATAGTCCTTGAA | 93664 |
rs527627382 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122362421 | GTTAAATGGACTAGG[G/T]TGAGGGGGGTAGGAT | 93664 |
rs527628368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122369575 | TTTTGACCCCATATC[C/T]CTCCTCTGAGCTCCA | 93664 |
rs527628714 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122466402 | TCGCTGTCTTTGCCA[C/T]TCCCCTCTGGGGCCA | 93664 |
rs527634479 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122445803 | CCTGAGACAGGGCGA[A/C]AGAGTAAGAACCTGT | 93664 |
rs527643750 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122800370 | GAGAGAAAATTTTAC[C/G]TCATAAACAGATAAG | 93664 |
rs527659687 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122349847 | GTCTTCGCTTTCCCT[A/G]TTCATGGGTAGATGG | 93664 |
rs527661780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122644676 | ACAAAAATAAAAACT[A/G]GTCCTTTTTCTTAAT | 93664 |
rs527662123 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122393939 | GACACATGTAAATAC[A/G]GCAATTAAGCAGAGT | 93664 |
rs527668706 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122454761 | ACTCAGAGTATTCGA[G/T]ATTTAAAAATTATCA | 93664 |
rs527674040 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122425293 | GCCATACATTTTTTT[A/G]AAGATTGATCTTTGC | 93664 |
rs527676738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122558647 | CCATCAAATTTAATA[C/T]ACAGGAGGAAAAACT | 93664 |
rs527680583 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122499025 | CACCAATCCAGGATT[G/T]CTTTTTATGTTAATT | 93664 |
rs527681424 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122552051 | GTTACCACATGGGTA[C/G]TGAGAAAACAGAACA | 93664 |
rs527690871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122719549 | CCTTCCTAACATGCA[C/T]GAGCAGAGGTTAAGT | 93664 |
rs527691802 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122769991 | TACATATATTAACTC[A/T]ATCCACACAACCACC | 93664 |
rs527702352 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122671077 | GTTACCCAGGCTTGG[C/T]TAGATCCTGTATCGT | 93664 |
rs527703756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122768565 | AGACAAAGAGGATTC[C/T]GACTTTCTAAATTGA | 93664 |
rs527712713 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122820652 | GCAAGCTCCGCCTCC[C/T]GGGTTCACGCCATTC | 93664 |
rs527718806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122552694 | TGTTCTTGAGACAAG[C/T]TGAAGGTCCAGGAGT | 93664 |
rs527720797 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122347018 | TAGATCTATTAAATT[A/G]GATAGATCCATCGAC | 93664 |
rs527729388 | in-del | -/T | 0.410905 | 0.191336 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122547074 | CTCAAATCTAGGGTG[-/T]TTTTTTTTTTGCCTT | 93664 |
rs527740187 | in-del | -/T/TT | 0.419109 | 0.20387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122519863 | TATTTGCCTAATTGA[-/T/TT]TTTTTTTTTAAAGGA | 93664 |
rs527744823 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122617948 | CTAGGGAGGCTGAGG[C/T]AGGAGAATGGTGTTA | 93664 |
rs527744934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122650487 | AAAGTGGAAAGTTGG[A/G]ATAACTTTCTAATTT | 93664 |
rs527755567 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122506135 | CCTCTACTCTGCCTC[A/G]TCACCACTTGCCAGG | 93664 |
rs527757975 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122326423 | CCTGTTTTCAAAAAA[A/G]GACAATCTGCCATTA | 93664 |
rs527760018 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122877788 | CAACTAGAAACGATA[C/G]CGTCTAATCAGGAGC | 93664 |
rs527765986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122605141 | TAAACAATACAAATG[A/G]TAAACATGTATAGGG | 93664 |
rs527771000 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122452920 | ATATGTTTGATGCTT[C/G/T]TTAACTAGTCAATTA | 93664 |
rs527774914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122775619 | CTTGTGGTTACCTTT[A/G]ATTTAGCATATCTGA | 93664 |
rs527786126 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122586810 | AAAGAATCTATTTCC[A/T]TTATATTGTCTGACT | 93664 |
rs527800352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122598640 | ATGTATTAATACTAG[C/T]AGGCCAGTCAGTGAA | 93664 |
rs527805143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122605650 | CTATGCCAAATCTAT[A/G]TATATTTTTTCTCTG | 93664 |
rs527807928 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122481498 | GTAATCCCAGCACTT[C/T]GGGAGCTGAGGTGGG | 93664 |
rs527809485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122827342 | TGGTTTCAAAGAAAA[C/T]TCTAGTAAATATTTA | 93664 |
rs527816900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122729097 | CTCTTAGATTCTACA[C/T]ATGAGGGAAATCATG | 93664 |
rs527816936 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122461071 | AAAATAGTTACAAGA[C/T]TTTGTATAGTTACAA | 93664 |
rs527817613 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122723510 | TTAGAATGGCAATCA[C/T]TAAAAAGTCAGGAAA | 93664 |
rs527829214 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122767360 | GCCCATGCAGATAAG[G/T]GATAGAGCTGGGATT | 93664 |
rs527840493 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122363826 | ATTAAGTCACAAGTT[A/G]ATGGGGGCTGCCTTA | 93664 |
rs527840522 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122371453 | CCAGATGCTTATAAA[A/C]CCATCAGATCTTGTG | 93664 |
rs527848968 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122792435 | TAAACCAGGAAGCAC[A/G]GCCTCACGAGAGGTG | 93664 |
rs527869862 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122656983 | CTGGAATTAATTTTT[C/G]TATAAGGTGTAAGGA | 93664 |
rs527876530 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122735658 | TCATCCCCCTGCTGA[A/T]CCAATTTCAGTTTCC | 93664 |
rs527881833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122742852 | TAACATAATAACATA[C/T]TATCCATAGTCTCCT | 93664 |
rs527883309 | snp | C/T | | | intron-variant, downstream-variant-500B | CADPS2, RNF133 | GRCh38.p7 | 7:122697419 | TTAATTGATACTTTC[C/T]GTATTAGAACATATT | 93664 |
rs527883990 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122720728 | TGTAATATTCCTAAA[A/T]GTGAATCACCTAGTT | 93664 |
rs527884972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122467545 | ATTGAGATTATTTTA[C/T]ATATAAAACTACAGT | 93664 |
rs527885590 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122401514 | TCACTTGCCTTATCT[A/G]TTATTGACAGAACAA | 93664 |
rs527885643 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122838854 | AACGGTCATACTGCC[A/C]AAGGTAATTTATAGA | 93664 |
rs527887859 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122833662 | CGGCCTCCGAAAGTG[C/G]TGGGGTTACAGACAT | 93664 |
rs527888689 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122783258 | TTTTGTAACCCAGTC[C/T]GATATCTGGCTTGTA | 93664 |
rs527892792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CADPS2 | GRCh38.p7 | 7:122885493 | TTTAACTTTTTTATT[C/T]ACTGAGGAAAATTTC | 93664 |
rs527915380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122693183 | GCTCCTTTATAAAAA[C/T]ACTGTTAACACTGTT | 93664 |
rs527919301 | snp | C/G/T | 0.00398731 | 0.0445001 | intron-variant | CADPS2 | GRCh38.p7 | 7:122841720 | AATAACTAAAGAAAA[C/G/T]GAAGAGTTGCCTTAA | 93664 |
rs527919456 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122325138 | GATATATGATCCTAA[A/T]AAATATGAAGTAATT | 93664 |
rs527924710 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122700749 | ATTTGGAGAGGAAAA[A/G]AGAAGCATTTACTAA | 93664 |
rs527926318 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | CADPS2 | GRCh38.p7 | 7:122566176 | CATCGCTAATCATCA[C/G]GGAAACGCAAATAAA | 93664 |
rs527926830 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122611429 | TGATCAAATGTGTAA[C/T]AATAAATTAGAGAAC | 93664 |
rs527927463 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122422386 | GTCAGCCTACTCTTG[G/T]GGACTGCTTGCTGGC | 93664 |
rs527929387 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122415029 | TTGTTAACAAACTCA[G/T]GGCTATTAGAAAGAG | 93664 |
rs527943802 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122617770 | AACTATAAGCCGGGC[A/G]CAGTGGCTCACGCCT | 93664 |
rs527950870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122751920 | TAGGGCCAGGTCAAG[C/T]CCTTATTTACTCCCA | 93664 |
rs527951558 | in-del | -/TTTATTAAGTGTGAAACTCCTCCTTAAAGACACTCAATCG | 0.031064 | 0.120694 | intron-variant | CADPS2 | GRCh38.p7 | 7:122603360 | AAAGACACTCAATCG[lengthTooLong]TTTATTAAGTGTGAA | 93664 |
rs527952067 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122427206 | CAGACAGAAGTATTT[G/T]GAAGTATATAATTTT | 93664 |
rs527953708 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122878099 | CGTCTTTACTAAAAA[C/T]ACAAAAATTAGCTGG | 93664 |
rs527956420 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122820704 | AGCTGGGACTACAGG[C/T]GCCCGCTACCACGCC | 93664 |
rs527957837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122800530 | TAGTAGATGTAGGTT[A/G]GGGGCTGAGAATTTG | 93664 |
rs527958293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122538082 | GTTTCCAATCCAGAT[A/G]TTATTGAAAATACAT | 93664 |
rs527960274 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | CADPS2 | GRCh38.p7 | 7:122521812 | ACTTATATTAGGTAT[C/T]ACATTTTATAGAATT | 93664 |
rs527966101 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122429004 | TGAGAAAACAAATGA[A/G]TAAAGTAAACATGTC | 93664 |
rs527970584 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122584809 | TATATATATCTTTTC[C/T]TTTTTCTTATTAAGT | 93664 |
rs527987634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122618104 | CCCACTTTCCACTTC[C/T]TAAGTGAACGTTTGT | 93664 |
rs528007323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122332774 | GAGCTGCACAAGCTC[C/T]TTCCAGTTCACTACT | 93664 |
rs528036495 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122483602 | AACATTTTTCTTTCA[C/T]TTTTAATTTATTTAA | 93664 |
rs528043570 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122784935 | TCCTTTTTCACCTTG[A/T]TGAACATCAATTATT | 93664 |
rs528047950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122470852 | GAGGCCAACATTAGG[A/G]AATTTTTATGGCATC | 93664 |
rs528048250 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122786113 | ACTTCTAGTAGTCTC[A/G]TCTATTTCATATAAC | 93664 |
rs528049634 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122597732 | TACCTTCAATTTCCC[C/G]TGTAATAACTCACAA | 93664 |
rs528059931 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122573252 | TGAATCTTTTTACAA[A/C]CTTCTCTGACCAGGC | 93664 |
rs528063464 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122624212 | TACATTTTAAATTTG[G/T]TGTTTTAAACTAGAA | 93664 |
rs528065584 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122601949 | ATGATTTTAAAAAAC[C/T]GTATTAATTTAAAAA | 93664 |
rs528066100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122443453 | ATCAAATAAAATTCA[A/G]CCACATTATATACCT | 93664 |
rs528073399 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122835483 | AGATAATCAAACTTC[G/T]CTGAGCTAAAGGCAG | 93664 |
rs528083896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122470015 | TAAACAGATTTTTTG[C/T]GGTAAAATTTTGTGG | 93664 |
rs528086222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122738395 | TAGATCTTAGGTAAT[A/G]CAGAAGCTTTTTTTT | 93664 |
rs528089234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122372922 | TGATGCTCATCAGTT[C/T]AATAAAGGACTTTGA | 93664 |
rs528093542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122652082 | ACCTTAGCATCTACT[C/T]ATTTTGGAGAACCTC | 93664 |
rs528094073 | in-del | -/CAA | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122782612 | GAGACCCTGTCTCAG[-/CAA]CAACAACAACAACAA | 93664 |
rs528094262 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122757828 | AGAACTCATTTTAAA[A/G]TAAAGACAAAGTGAT | 93664 |
rs528099116 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122567351 | AGCTTTTAATTTATA[C/T]GAAAAAAGGCACTGA | 93664 |
rs528099290 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122458581 | TTGCAAACACTCCCC[C/G]CTTCCTTGTCTGGAT | 93664 |
rs528105482 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122598127 | TTTTGTGAGTCCTTA[C/T]TTCCATAGGCAAAAG | 93664 |
rs528114736 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122613650 | TTAAGGCTGGATTGG[C/T]TGGGGGTTGATAGCT | 93664 |
rs528115062 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | CADPS2 | GRCh38.p7 | 7:122318864 | AAGTTTCAGAATAAA[C/T]GTTTTCATAAATGCA | 93664 |
rs528121538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122730454 | AAATTTATCCAAGAT[A/G]ATAAACTTATGACTA | 93664 |
rs528126066 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122599783 | AATGTTACATATAAT[A/G]TGAAATATACATACA | 93664 |
rs528136650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, RNF148 | GRCh38.p7 | 7:122701505 | AAATGACGAGTTACT[A/G]GGTGCAGCACACCAA | 93664 |
rs528142795 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | CADPS2 | GRCh38.p7 | 7:122318163 | GCAGAGAACATAAAA[A/C]TCTGGAAAGAACCTC | 93664 |
rs528154821 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122794369 | TTCAAGCTCTGAGAT[G/T]CTTTCCTCCACCTGG | 93664 |
rs528164884 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122440029 | CGATTTCCTGCTGCA[A/T]CCCATGTTCTTCCGA | 93664 |
rs528171601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122523875 | GAATTTACTGAGTAG[C/T]CCCCTCTACCCCAAC | 93664 |
rs528177958 | snp | C/T | | | intron-variant, upstream-variant-2KB | CADPS2, LOC105375481 | GRCh38.p7 | 7:122529776 | GCTTGAAGATCCACG[C/T]CAAAATTACATTCCT | 93664 |
rs528180662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122423866 | GCTGGTGTAGGGAAT[A/G]CACTTCGAGAACTAC | 93664 |
rs528182236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122737942 | CCATGAACAAACATA[C/T]ATCAATACCTGAGTT | 93664 |
rs528184717 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | CADPS2 | GRCh38.p7 | 7:122886611 | AGCGTTGGGGGTGAG[C/T]TTGGGCGCCTCAGGA | 93664 |
rs528187398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122335409 | ATGTGCCACCACACC[C/T]GGCTACTTTTTGTAT | 93664 |
rs528190061 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122720139 | GTAAAACCAATAGAA[C/T]GTCATACTAAAAGTG | 93664 |
rs528196172 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122431056 | CCACTTCTTCCTGCC[A/G]TGATAAGAGCAAGAA | 93664 |
rs528197495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122694889 | TCACAGTAGCAGCAT[A/G]TAAAAATTTCTCTGC | 93664 |
rs528199522 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122440668 | TTTTTAATAGAGATG[C/T]TAATAAACAATATAG | 93664 |
rs528199603 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122469319 | AATATTCTGATTATA[C/G]AGTTTGCTTTGGGTT | 93664 |
rs528200062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122379887 | GTGCTCTAGAAATAA[A/G]ATGAGCTCCCAATTG | 93664 |
rs528201686 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122746847 | CAAGGTAAGTGCTGA[G/T]GAGTTATTTAACAGG | 93664 |
rs528204321 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122664644 | AGAATCCTCCATAAG[C/G]CATATAAGACTGCTT | 93664 |
rs528211712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122326026 | GAAGATGTGTTATGC[C/T]ATAAGTCATGTAGTC | 93664 |
rs528216325 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122754984 | TTCATAATGGCTCAT[A/G]GTCTCCTTTAGAACT | 93664 |
rs528217200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122478077 | TATAACATACCTATA[C/T]GTTACTCTTGAGAGA | 93664 |
rs528225394 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122809201 | TGGCAAGGGTCTAAG[A/T]CAAAAGTGTGCTCCC | 93664 |
rs528238361 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122572604 | ACCCAGGAGTATATA[C/T]TACCCAATATTTCAC | 93664 |
rs528244759 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122669846 | CTCTAAATAAGTCTC[A/C]GAATTCATGACTTTT | 93664 |
rs528250227 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122389569 | AAGAGTACATATAAT[A/G]TTTTGGCAAATGGTT | 93664 |
rs528256372 | in-del | -/TTT | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122367736 | TTTTTTTTTTTTTTT[-/TTT]GCTTAAAACAATAAA | 93664 |
rs528266535 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122686296 | GGATTTCTTTGCACA[A/G]TCATGCAGAAGTCAG | 93664 |
rs528276535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122753211 | CAAAGATTACTTTTC[C/T]AGGAAAAAGAGATGC | 93664 |
rs528281245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122579372 | GTTGGGAAACCCTGT[A/G]ATAGATAGAAAAGTT | 93664 |
rs528284291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122632951 | CATTTATTGAAGAGG[A/G]AGTGCTTTCCCCATT | 93664 |
rs528288641 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122387224 | CTGCTATACAGCTCA[A/C]CTGTTTTGTAAAAAG | 93664 |
rs528305027 | in-del | -/C | 0.00478085 | 0.0486577 | intron-variant | CADPS2 | GRCh38.p7 | 7:122692824 | CATCCACAGCTCTCA[-/C]GCACTGTTCTCTCTG | 93664 |
rs528308318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122664127 | TGAACCCAACATCCA[C/T]ACCTGTGTCTGAGAG | 93664 |
rs528313455 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122692535 | GTCTACTGCCTCCCA[C/T]GTTTCCACTGGGGCC | 93664 |
rs528321377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122626234 | AGTGCAGAACATCAC[C/T]GGCTGTTGTGTTAAT | 93664 |
rs528328828 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122430341 | TTAAATCACAATATG[C/G]TATATAATTTTCAGG | 93664 |
rs528335287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122707158 | TACTTAACCATTAAC[C/T]GCAACAAACATGTAA | 93664 |
rs528342064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122713180 | CTTTAAATTTTTATA[C/T]TTAAAAACAAAGCTT | 93664 |
rs528346885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122675378 | AAAAGGCCAGTGTGC[C/T]TCCTCTGATTTCAAG | 93664 |
rs528349408 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122769251 | AGCTAAAAATTAGAG[A/T]CAAATCTCACCCTCC | 93664 |
rs528350213 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122639206 | AATTAGTTGGTTAAC[A/G]TTCTTTTTTACATGT | 93664 |
rs528352980 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122808688 | TTATGGCTTTTTCTG[A/G]AATCCCAGCAGTTGC | 93664 |
rs528357837 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122545666 | GAGACTGAATTAGGG[C/T]TGGCAGAAGGAATAA | 93664 |
rs528358213 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122862695 | TTTTGCTGGACCCTA[A/T]CTCAATAATGATCAA | 93664 |
rs528358312 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122394707 | CTGAGGGAGGGGGAG[C/G]GGCAGCCCATGGCAG | 93664 |
rs528361578 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122866696 | AAAGGGCAAGACTGT[C/T]TCAAACCAAAACAAA | 93664 |
rs528362092 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122854029 | ACAGACTCCAGGCCA[C/T]AGTAACTGCTGGAGC | 93664 |
rs528365749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122437886 | AAGCAATTAAAAACC[A/G]AAGGAAGTTCTATGA | 93664 |
rs528366193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122720134 | TAGAAGTAAAACCAA[C/T]AGAACGTCATACTAA | 93664 |
rs528370294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122632455 | TTTGCATTTCTCTGA[C/T]GATTAGTGATGTTGA | 93664 |
rs528379233 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122546468 | AGAGATTCCTTTTCA[A/T]CATTCCTGTATTTTT | 93664 |
rs528381251 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122375252 | ATAACCAAAACAATT[A/C]CGAGCAAAAGAATAA | 93664 |
rs528385841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122446582 | TTAGCATTAGAGATT[C/T]CCCCCATAAGCCTTT | 93664 |
rs528387227 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122625583 | ATTTTGCCTCAAGAC[A/T]AAAACACAGAAACCC | 93664 |
rs528390034 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122859856 | AATTTTTTCCCAAGT[A/T]TCTTCAATCTGCAGT | 93664 |
rs528402514 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122815844 | AAAGAAAAGACAAGG[A/C]AGTTCTGCTTTCTCG | 93664 |
rs528403087 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122593211 | ACAAAACAAAAAAAA[A/T]TCTGCATGGCAATAT | 93664 |
rs528403399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122538841 | GAACACTATTTATAA[C/T]GATGGGAGTTGGAGA | 93664 |
rs528414686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122669528 | GTCTAGGAAGTGATG[C/T]ATTGAAAGGCATGAG | 93664 |
rs528422029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122854602 | TGTGCTGCACACATG[C/T]AAGGACAAGAGAGGC | 93664 |
rs528426136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122731268 | TTTTAAGAAGCTCTA[A/G]CATCCATATTTTGTA | 93664 |
rs528426177 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122709753 | TGAGTTCACGTCCTT[C/T]GTAGGGACATGGATG | 93664 |
rs528436252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122761224 | AAGTGGGATGCAATA[C/T]TGAAAAGGAAAGAAT | 93664 |
rs528438470 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122521440 | ACTACATTCTTTCTT[C/T]TATTTGACCCCACAA | 93664 |
rs528444444 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122752698 | AAACCCTTTCAGTTA[C/T]GGTATTGTCTTCAGA | 93664 |
rs528446627 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122672182 | ATGAAACTAACAATG[A/G]TGGGTTTACTCTCAC | 93664 |
rs528452445 | in-del | -/A | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122630377 | TTTATATGAAGAGTC[-/A]AAAAAAAAAAAAAGA | 93664 |
rs528455082 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122716240 | GCTGAAGGAATATTT[G/T]TTTTATGAAAAAAAG | 93664 |
rs528459663 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122730981 | AATTTCATAATAAAC[A/G]TATTGAAAAATTTTT | 93664 |
rs528463251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122755796 | TGTGTTCTATACTGA[C/T]AGGAATATGTAAAGG | 93664 |
rs528464734 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122803742 | TAATGAAGAAAACAA[C/G]TACTTTGCAACTAAG | 93664 |
rs528466381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122708781 | TCCTTATTCAGTCTA[C/T]CGATTTAGAAGATAG | 93664 |
rs528467902 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122389314 | GCTTTTTCTGGCTTA[A/T]TAAAACCCAACTTAG | 93664 |
rs528485960 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | CADPS2 | GRCh38.p7 | 7:122705435 | GATAATATATAATAT[-/G]TAATATAATATTATA | 93664 |
rs528490115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122666413 | CAATGGCACCATGTC[A/G]GTTCACTGCAAACTC | 93664 |
rs528499244 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122659233 | CCCTAATGTAAAAAG[G/T]TGAAAACATGCAAAA | 93664 |
rs528503698 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122582008 | TGATTTACAAACTTA[A/C]CTGGCACACACCTGA | 93664 |
rs528503742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122573999 | ACTGGAATACATTCT[A/G]AAGACAAATCAAATG | 93664 |
rs528508461 | snp | A/C | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122542756 | ATAGTCTACATCAGT[A/C]TAGAATCTCTCTGAT | 93664 |
rs528514145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122628441 | ATACATGTTACGAGA[A/G]AGAGAAATAGAGAGG | 93664 |
rs528517456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122709414 | AGGAAACAACAGGTG[C/T]TGGAGAGGATGTGGA | 93664 |
rs528533462 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122774565 | ATGTTCTACCAATTA[C/T]GGTTTGCCCAATTAC | 93664 |
rs528534276 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122722313 | GTCTCAGCCCAAAAT[C/T]TCCTTAAGCTGATAA | 93664 |
rs528534324 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122750990 | ATTTTTTTTGGACCA[A/G]CATAAAAACGAAAAG | 93664 |
rs528537001 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122437219 | ACAACATGATATCAT[-/A]AATTAATGAAGTTAA | 93664 |
rs528552525 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122856259 | CCAACATAAGCCTCA[C/T]TGGAATATCCCCAAA | 93664 |
rs528555238 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122540081 | AATTTATTTTAGCTG[C/T]GTATTTGAGATTTAG | 93664 |
rs528561550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122817456 | TGGGAGAGACAAAGG[C/T]GACACGTTTTATCCG | 93664 |
rs528563865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122432256 | CCTTGTGCAAGTTAA[C/T]GCTTTTTTTCAGAAG | 93664 |
rs528573595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122448732 | TGCACAGAATTTCTC[C/T]GGCCACTGGTTTTGG | 93664 |
rs528580071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122810597 | TATGTAATAATGTAA[C/T]AATGTTTAAGAAAGC | 93664 |
rs528585432 | snp | A/G | 4.99896e-05 | 0.00499923 | missense | CADPS2 | GRCh38.p7 | 7:122345590 | TCAAATAACTTTTCT[A/G]TATACATTTCCTCAT | 93664 |
rs528587143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122345229 | CTTCCCGGCTCAAGC[A/G]ATTCTTGTGCTGCAG | 93664 |
rs528592745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122857361 | AGGTCTGGAGATGTA[C/T]GAGTAATAAAGAAAC | 93664 |
rs528612912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122448783 | ATATAAAAAATACTT[C/T]GCTAGGATCTTCTAA | 93664 |
rs528613336 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122439836 | TTTCATATGCGGAAC[C/G]ACGAACGTTACTATT | 93664 |
rs528635283 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122816619 | TCCATACTGTTTTCC[A/C]TAATAGCTTTGTGAA | 93664 |
rs528641770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122594238 | TCAGATGATCAAGAC[C/T]AGCTTGGGCAAAATA | 93664 |
rs528645958 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122822451 | AACCCTGAGAAACAT[C/G]GCCCATTCTCTCTCC | 93664 |
rs528651302 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122683616 | TGACATAGTGAAATA[A/C]ATTTTAAAATCACTG | 93664 |
rs528651431 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122352380 | AAAGTTTAGATGGAC[G/T]GGGATGGGTTTACTC | 93664 |
rs528652415 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122448335 | AGAACAGCATGGGGG[A/C]AACCTCCCCTACCAT | 93664 |
rs528653500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122646073 | TCACTTTTCCAAAAC[C/T]TTCCCAGAGCAGATT | 93664 |
rs528654933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122725787 | ATACAGAGAGACACC[A/G]TGGTCTTGCCTCACA | 93664 |
rs528660450 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122676676 | ACCTGGAGGCCTGCT[G/T]TCAGCTGCTCAGCCA | 93664 |
rs528662234 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122639944 | ATAGCACGAAACTCT[A/T]GCAGGAGTTCCAGAC | 93664 |
rs528672448 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122830404 | ACACTGCTAAAAAAA[A/G]AAAATCAAAGGATGC | 93664 |
rs528681693 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122660740 | ATGGTGAAACCCCAT[C/G]TCTACTAAAAATACA | 93664 |
rs528683106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122493123 | AGGCAAAGCAACAGA[C/T]TAAGAGAAGATGCAT | 93664 |
rs528687488 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122341089 | CTGTTTAAAACATCC[C/T]GGTCAGCTGGAAACA | 93664 |
rs528691187 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122864720 | ATTACAAAGAGATAT[G/T]TATACTATTTAAATT | 93664 |
rs528691219 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122492811 | ATCCAGTGATCCTCC[C/T]ACTCAGCCTCCTGAA | 93664 |
rs528691398 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122859898 | TTGGACCCCATGGAT[A/G]TGGAGGGCCAACTGT | 93664 |
rs528696859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122634287 | TAAATGCTGAGCTAA[A/G]AAGCTGCTATTTCAG | 93664 |
rs528698602 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122761984 | GCCTGGGTGAAAAGT[C/G]AGACTCTGCCTCAAA | 93664 |
rs528714531 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122770992 | TGGAGGCTGCCAGAA[A/G]TTCTGAAGCTGTGGA | 93664 |
rs528715808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122547237 | GAATAAATGTTGACA[A/G]GCAACAAGCCTCCCT | 93664 |
rs528718777 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122640470 | GTGTGCACACACATA[C/T]ACACACACACACACA | 93664 |
rs528728826 | snp | A/G | 1.70997e-05 | 0.00292396 | missense, intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554629 | CCTGGCTATTTTTTG[A/G]AACTACCATTCGGTG | 93664 |
rs528744725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122642402 | CATGGGAGCAGCTCT[A/G]GGAAATAGGAAGGTC | 93664 |
rs528753782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122410471 | TTTTGTAGTAAATAT[A/G]GTTTACAACAGTGGC | 93664 |
rs528759808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122871854 | GCTACTTCTTCTCCA[C/T]TTCCTTCTCCAGCTC | 93664 |
rs528781292 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122690001 | GGCCTGGACAGTGTG[C/G]AGTTCTGCACAGAAG | 93664 |
rs528789666 | in-del | -/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122449178 | AATAATGGGGACTTA[-/T]TCAGTTACTAATATA | 93664 |
rs528809975 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122454897 | AGCCACTATCTGCTT[A/G]TCCCTGAGTACGCAG | 93664 |
rs528811089 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122463481 | ATAAATAACCTTGTG[C/T]CAATAAATTATGAAA | 93664 |
rs528821464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122372399 | GGGCACAGAGAGGGA[A/G]GGCCAAGACCTTTTC | 93664 |
rs528824116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122872595 | TGTTATATTTCAGAA[C/T]TTTTTCTTATGATAT | 93664 |
rs528827088 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122491100 | ACATTTCAATCCTGC[G/T]CTAAAATAATAACAA | 93664 |
rs528845503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122657376 | TTGATGGGGATGGCA[C/T]TGAATCTATAAATTA | 93664 |
rs528849139 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122780808 | CTGTATAATAGTATA[C/T]GGTATGTGGCTGCAC | 93664 |
rs528851090 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122664050 | GTAAGAAATAAATGA[C/G]CATTGTTTATAAGCA | 93664 |
rs528872007 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | CADPS2 | GRCh38.p7 | 7:122318088 | TTTGCTTTGGAAGCC[A/G]CTGTGGGTGAAGAGT | 93664 |
rs528880363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122371694 | AGGGCCTGAAGACTA[C/T]AGTACTGCCAGTGAG | 93664 |
rs528881660 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122786677 | TTCGTGTTTAAGACA[G/T]GAATACAACTACTAC | 93664 |
rs528887012 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122605987 | CTATTTAAATGTCCC[C/T]AAACCACACAGTGAT | 93664 |
rs528895845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122794282 | AATCCCATATTTCTC[A/G]GAGGTTTTGTTCATT | 93664 |
rs528898596 | snp | C/T | 0.000399281 | 0.0141238 | missense, upstream-variant-2KB, utr-variant-5-prime | CADPS2 | GRCh38.p7 | 7:122886193 | CCGCGCCGCCGCCGC[C/T]CGCGCGCCCCGGCGC | 93664 |
rs528899019 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122612278 | ATTTGCAGATGACAT[C/G]GTCTTGTACATAGAA | 93664 |
rs528901620 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122833018 | ATCTATTTCCTATGA[A/C]AAATTGTGAGAAACA | 93664 |
rs528908671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122565805 | GAACATTTAAGATAT[A/G]TTCTCTTAGCAAATT | 93664 |
rs528913642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122706607 | TATCACACACACTTA[A/G]GAGATAGGTTGTGTG | 93664 |
rs528919149 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122781585 | CTCATAATTCCAGAG[A/G]TACAAATATGCAACA | 93664 |
rs528920866 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CADPS2 | GRCh38.p7 | 7:122657818 | CTTTCTCCTGCCTGA[C/T]TGCCCTGGCCAGAAC | 93664 |
rs528927674 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122492762 | TGGAGGACAGTGGCA[C/G]GATTATGGCTCATTG | 93664 |
rs528932326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122523057 | TATCTCTTTGATTCA[C/T]TGATTTCTGTTTCTT | 93664 |
rs528935438 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122334484 | AAATATTGTTGCTGT[A/G]GAAATAGTGAGTTCT | 93664 |
rs528942102 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122490844 | CTTAGATATTAATGT[C/T]ATTAATATTCATTCA | 93664 |
rs528955833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122845942 | CTCGCCAACACGGTG[A/G]TCCCTCATTCAACAC | 93664 |
rs528956779 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122854397 | AAATGAAGGTCTTGC[A/G]TTCACTGCCTTCTAC | 93664 |
rs528958246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122530899 | GTATTCTGGGGAGAG[A/G]GACCTCCTGTGCTAG | 93664 |
rs528958673 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122618845 | TGCACCATCGTCACT[G/T]AACACGATTTTACTT | 93664 |
rs528963864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122669447 | GCATCTAGCTCACAG[A/G]TGTCCTATGATGCTG | 93664 |
rs528964523 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122461138 | TCACAATAGCAGCCA[A/G]TTCCTCAACTGGAAG | 93664 |
rs528979283 | in-del | -/A | 0.0810805 | 0.184299 | intron-variant | CADPS2 | GRCh38.p7 | 7:122658918 | GATTTAATAATATGT[-/A]AAAAAAAAAAGTTTC | 93664 |
rs528980355 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122494961 | TTGTGTGGGTGTTTT[G/T]GGGGGTAAGGGTTAA | 93664 |
rs528985866 | in-del | -/GTGTACATTACA | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122640325 | TTTCTTTGGGTGTGT[-/GTGTACATTACA]GTGTTTCTCTAGCCA | 93664 |
rs528991937 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122468029 | TATTCTTTTATTTCT[-/G]GAAACACTCAGAGTG | 93664 |
rs528994223 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122839026 | CTACCTCACTTCAAA[A/C]CATACTACAAGGCTA | 93664 |
rs528997567 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122531268 | CACAATGGAAGAGAA[A/G]GAAGAAGAGGTGAAG | 93664 |
rs528999104 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122437841 | AGTTCTCTCAAGAGA[G/T]CTAATCTTTCAAATG | 93664 |
rs529003355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122333789 | TAACTGAATCTTACT[C/T]GTATTGCTATCTCCA | 93664 |
rs529004102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122753076 | GTTATTCAATGGCCC[C/T]GGGGTAAAATGATTA | 93664 |
rs529004198 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122483339 | AATGCAAGCTAGAAG[-/A]AAGTGGAGCAACACC | 93664 |
rs529006169 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122660636 | AAAACTTGGGCCAAG[A/C]GCTGTGGCTCACACC | 93664 |
rs529016507 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122429484 | TTTAAAGCAAACAAT[G/T]TGTATCTAACAATTT | 93664 |
rs529023999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122578751 | TCATAGTGACTGAGG[C/T]ATGAAGGTCAAATCA | 93664 |
rs529027076 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122592687 | TTCATGTCCTTTATG[C/G]GGACATGGATGAAGG | 93664 |
rs529038309 | in-del | -/T | 0.00756961 | 0.0610533 | intron-variant | CADPS2 | GRCh38.p7 | 7:122649910 | TGATTTTTTTTTTTT[-/T]TTTTTTTTTTTTTTT | 93664 |
rs529044588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122483773 | ATACATGAAGATATA[C/T]AATAAATTTAAAGGG | 93664 |
rs529046580 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122491769 | TTTCACTTCATGGTT[C/T]CTTACAGCTTTTAAT | 93664 |
rs529063969 | in-del | -/AA | 0.011519 | 0.075012 | intron-variant | CADPS2 | GRCh38.p7 | 7:122790398 | CCAGACAGCGTTTCT[-/AA]AAAAAAAAAAAAAAA | 93664 |
rs529065608 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122632841 | GAAGTCTTACATTTA[A/G]GTCGTTAATCCACCC | 93664 |
rs529069478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122631688 | TGGGACACTACATTG[C/T]CTTTTCTTTTTTTTT | 93664 |
rs529071099 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122668949 | TTCCTCCATCAAAAC[A/G]GAAGGTAAGCACCTC | 93664 |
rs529071587 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122394628 | ACAGCTAGCAAACAA[A/G]TTTTGGGAAGGAATA | 93664 |
rs529071798 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122572903 | TTCGGATGAAAAATC[G/T]CCATATGCCACCTCT | 93664 |
rs529080835 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122728372 | TGAAGAGTTGAGGTA[C/T]AATGTTAGGGGAAGA | 93664 |
rs529082341 | snp | A/C | 2.62092e-05 | 0.00361993 | intron-variant | CADPS2 | GRCh38.p7 | 7:122491424 | ATATTGGCTAACCTG[A/C]TCGAGAAAAAAAAAG | 93664 |
rs529094564 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122750595 | AAAAAGCAGCTCAAA[A/G]GAAATTTCCACAGCA | 93664 |
rs529095336 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122393723 | AGTAGATCATACCCC[C/T]CATATTGAATATCAT | 93664 |
rs529097415 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122586568 | CTGAGCCGAGTTACC[A/C]TGTTTTAATTATTGC | 93664 |
rs529100238 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122713006 | AGGTTACGGCACACA[A/C]AAAAATAAATCCTGT | 93664 |
rs529104754 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122624909 | TAGAAAGTCATAAGT[A/G]GCATGGAGAAAAAGT | 93664 |
rs529116959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122808648 | AAATCCAGTTCAGAT[A/G]TCTCTGAACAGAGGT | 93664 |
rs529131719 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | CADPS2 | GRCh38.p7 | 7:122722294 | ATATCTAGAAAACCC[C/T]ATCGTCTCAGCCCAA | 93664 |
rs529139307 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122863841 | TTGAGAACAGCCTGG[C/T]CAACATGGCAAAACC | 93664 |
rs529139983 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122776263 | GCTTTATAAAGGGCA[C/G]ATCCCCTACACATGC | 93664 |
rs529149388 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122719011 | TCCTATGCCATAAAT[A/G]TACACAATTTTGAGG | 93664 |
rs529153833 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122348935 | ATTATCGCTGGTTCA[A/G]TGCTCCCATGTGCTA | 93664 |
rs529158430 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122351232 | CAAAAAATTAGCTGG[G/T]CATGGTGGCGGGTGC | 93664 |
rs529159679 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122681399 | ACTAACTGTGCCCGA[A/T]GCGTGCCCAAGGACA | 93664 |
rs529160133 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122440329 | TGTATTAGGTACCCA[C/T]GATGGGATGTTGTTC | 93664 |
rs529160608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122723876 | AGTTCATGTCCTTTG[C/T]AGGGACATGGATGAA | 93664 |
rs529164134 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122814779 | TTGTTTTCATTACAT[A/G]GAATTGAAAATAAAC | 93664 |
rs529166923 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122341939 | ACCTGCCATAACTTA[C/T]TTATACTTTTAAAAA | 93664 |
rs529169272 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122680829 | AAAGACACAGGCACA[C/T]GTATGTTTATTGCGG | 93664 |
rs529172021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122400889 | AAGATTAACCTAATA[C/T]ACAATATGGTGACCT | 93664 |
rs529173952 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122754559 | TCGGCTCACTGCAAC[A/G]TCCGCCTCCCAGGTT | 93664 |
rs529174080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122638214 | GGCTGGTAGACAAGA[C/T]TATACCCTTTCTGGA | 93664 |
rs529175400 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122823231 | AAGAAACATCTAATG[A/G]TCATCTCATAGTAAT | 93664 |
rs529178557 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122497381 | GCCATGCCTCTTTTT[C/G]TTTCATTCCCTGTCT | 93664 |
rs529180789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122674712 | AAAGGATTTTATAAT[A/G]ACGAGAAAAACATTA | 93664 |
rs529182748 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122357046 | GAGCACATTAACGCA[A/T]GCATATACATATATC | 93664 |
rs529186639 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122861346 | GATTTGCATTTCCCC[A/G]ATAATTAGTGATATT | 93664 |
rs529187577 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122592202 | AGACACTTCTCAAAA[C/G]AAGACATTTATGCAG | 93664 |
rs529206817 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122725893 | CACGCCCTGCAGGAC[A/G]CCTGGATGACACCTC | 93664 |
rs529224494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122768413 | TTGTTTCAAAACTGA[C/T]TTAGGACATTTCTAA | 93664 |
rs529227688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122762592 | GAGTTGGATAAGAAA[A/G]AAACATTTTTCAAAA | 93664 |
rs529227996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122754160 | TATTTAGTTTTCATT[A/G]CAATTAATTTGCTTT | 93664 |
rs529234524 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | CADPS2 | GRCh38.p7 | 7:122329001 | GAAGGTGGTATTGAC[-/A]AATGAAAGAGTGTTG | 93664 |
rs529240052 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CADPS2, RNF133 | GRCh38.p7 | 7:122700441 | CAAAGGCCATTAATC[C/G/T]GATTTTATTTTCATA | 93664 |
rs529240338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122634184 | AGGATAATGCTGGCT[C/T]TGTAGGATGAGTTAG | 93664 |
rs529246353 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122405556 | TAATCCCAGCTACTT[G/T]GGAGGCTGAGGCATG | 93664 |
rs529256274 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122809799 | ATGCAAGTGTCCAGT[A/C]CACCCTCATAGGGTA | 93664 |
rs529256792 | in-del | -/AATA | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122840837 | ATATTTTGCAGAAAT[-/AATA]AATATCTACAGAAAA | 93664 |
rs529257640 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122670675 | GCTAATTTTTTTTGT[A/C]TTTTTAGTAGAGACG | 93664 |
rs529257851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122396061 | GTGATCCACCCGCCT[C/T]GGCTTCCCAAAATGC | 93664 |
rs529267356 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122388453 | TCAAGATAACCTAAT[A/T]CTCATTAAATGTTGG | 93664 |
rs529269391 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CADPS2 | GRCh38.p7 | 7:122722225 | AGAAAGAAAGGGTAT[C/T]CAATTAGGAAAAGAG | 93664 |
rs529275155 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122590956 | ATTAAATTAGTTTAA[A/C]TTGGGTGATCAATAA | 93664 |
rs529279433 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122588041 | TTTATGTCCTTTGCC[A/C]ACTTTTAAATTTTTT | 93664 |
rs529282728 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122848110 | GCCTATAGCTAATGT[A/C]TTAATCTTATTAGAA | 93664 |
rs529287338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122539943 | CTTCATAAAACTTCA[A/G]CTGATGATTTTAGGT | 93664 |
rs529289571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122580388 | CGAATCTAGGAGGTG[A/G]GTTGCAATGAGCCGA | 93664 |
rs529298121 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122486166 | GCCCACAGATCAAGG[A/G]GTAATTTCAACTTTC | 93664 |
rs529299172 | snp | A/G | | | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122704019 | AAATTGGCAACACCC[A/G]CTCAAAAATTTATTT | 93664 |
rs529299959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122856472 | ACCACCTCATTCATG[C/T]TGTAGTTCCCTACAC | 93664 |
rs529309270 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122803239 | ACCCACTTAATCCCT[C/G]TCCTGCTGCTTTAAA | 93664 |
rs529315485 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122395504 | TTTATTCCTGGAGAT[C/T]CAATCATCGAGCTAG | 93664 |
rs529316133 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122734945 | GGTCACCAAGTCAAA[C/T]CACCTCTTCAATGCT | 93664 |
rs529318068 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122626962 | TGAAACAGAGATTTT[C/G]CCCTGTAGTTTCACT | 93664 |
rs529325666 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122485495 | CCAGAGCAAGGCCCT[G/T]CCTTTCTTCGATTCT | 93664 |
rs529332320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122863825 | ACCTGAGGTCAGGCA[C/T]TTGAGAACAGCCTGG | 93664 |
rs529334740 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122500435 | AACTAACAGTTTAAC[A/C]GCACACATAACTCAA | 93664 |
rs529341604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122770391 | TATTTTTTATTTTTG[A/G]AAAACCTCACTTTAA | 93664 |
rs529342793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122432502 | AAAAATTAGCCAGGC[A/G]TGGTGGCAGATGCCT | 93664 |
rs529344314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122810292 | AGCTTGTGGCTCCTA[C/T]TGACCTACTTCCACC | 93664 |
rs529347776 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122492425 | CTGCTCTGAAGTCAC[C/G]TCCCTGAGTGTGTCT | 93664 |
rs529349046 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122675946 | ACGCCCATGCAACAA[A/T]CCTGCACGTTCTGTA | 93664 |
rs529350254 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122533298 | TTAAAGGCTTGATAA[A/C]GACAAATCTCTTTAA | 93664 |
rs529350307 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122812505 | TAGCCCAGGACCTGT[C/G]ATGAATTAGGTGGGA | 93664 |
rs529362086 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122720601 | ATGTATATACATACA[C/T]ATATACGTATACATA | 93664 |
rs529366040 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | CADPS2, LOC105375481 | GRCh38.p7 | 7:122529386 | GCATTTATTTCACTG[-/A]AAAAAAGTATACCCA | 93664 |
rs529367177 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122600767 | AAAGTTTCGTTTAAT[A/G]AAGAACTAATGAGCC | 93664 |
rs529367480 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122448233 | CTTTCTGGAAGATCT[G/T]AGGATTTTTTAATCC | 93664 |
rs529380242 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122402562 | AGAAACCAATTAGGA[C/T]GACTGAATTATTCAT | 93664 |
rs529381983 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122749159 | AATCAGCATCCTCCT[C/T]CTGTCATATTTTCTC | 93664 |
rs529382711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122438711 | TTTATGCATATCAAA[A/G]CCTCCCCTAGACCAG | 93664 |
rs529387125 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122798107 | TGCAGTTGTTGCATT[A/T]AAAAAAAACTCTATA | 93664 |
rs529391447 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122416986 | AAAGATAAATGTTGT[C/T]GGGGATTCATAGGCT | 93664 |
rs529395447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122593466 | TGAAAAGACCCGGGG[C/T]GAGCAACTTTACCAC | 93664 |
rs529395574 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122344209 | ACGAAAACATTTGCC[G/T]TAACTTGCATAATTA | 93664 |
rs529399658 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122588713 | TTTAACTAGGTCTAA[A/G]GTCTTTCTGCTGTCC | 93664 |
rs529400426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122730127 | CATCTTCTTAGTGTA[C/T]AAACAATGCCTATAT | 93664 |
rs529410089 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122351368 | ACAGAGCGAGACTCC[A/G]TCTCAAAAAAAAAAA | 93664 |
rs529412463 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122615855 | TATTAAATAGAAAAT[C/T]ATAATTTGTCACTGA | 93664 |
rs529413879 | snp | C/T | 1.68698e-05 | 0.00290424 | missense, intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122554565 | CCACTATGCTTCATA[C/T]GTGCTGGTTTATCCA | 93664 |
rs529417171 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122855857 | ATTTTTGGTGACTTA[A/C]CTCTCATTCCAAATC | 93664 |
rs529420371 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122816535 | TATTATGATCTCCTT[G/T]CTTTTGGACATACAG | 93664 |
rs529421844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122447480 | TGTCACTTTGAGGGT[C/T]TCAATTAACCATCAC | 93664 |
rs529435476 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | CADPS2 | GRCh38.p7 | 7:122411677 | GCAATTCTGTACTTT[-/G]TTGATAATCCTAAAG | 93664 |
rs529441040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122600199 | ACAACACATGCAGTA[A/G]CTAAGTCAAGGAATT | 93664 |
rs529450265 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122852764 | ACTATAAACACTTAC[A/G]CTTTTACTGGGAGTG | 93664 |
rs529455683 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122725248 | TAATGTTTTCCCATC[A/C]TAGTTCACAGACCCC | 93664 |
rs529455740 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122639390 | AAAAAGTAGAAAAAC[A/G]TCCATTATATGCTCT | 93664 |
rs529472515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122720339 | GTATTAATGCTGTAA[C/T]TGTATATTCTTAAAT | 93664 |
rs529487276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122500056 | GTAAAGTACTCCAGA[C/T]GGACCATCCAGCAAG | 93664 |
rs529495855 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122679286 | GGGGGGGCTCTAAAA[G/T]GGCCACCCTGGGAGT | 93664 |
rs529518677 | in-del | -/ACA | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122668052 | CAGCACCAAGGGTAG[-/ACA]ACAAGTGACCAGAGC | 93664 |
rs529519828 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122345384 | CTCAACTGATCCACC[A/G]GTCTCAGCCTCCCAA | 93664 |
rs529521824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122821568 | AGGCCTTTCCTACAG[A/G]GTCTGAGATGGCCAC | 93664 |
rs529522291 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CADPS2, RNF148 | GRCh38.p7 | 7:122703356 | TGGTTCAACACTACC[A/G]AATATGGCATTCTGT | 93664 |
rs529538121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122605836 | GTGCTATTTCTTCCA[A/G]TTAGTTCATGTATCC | 93664 |
rs529540029 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CADPS2 | GRCh38.p7 | 7:122878567 | ATGGCGTGAACCCAG[A/G]AGGTGGAGCTTGCAG | 93664 |
rs529546872 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122835446 | GGAGAATGACTTTGA[C/G/T]GAGTTGAGAGAAGAA | 93664 |
rs529551217 | in-del | -/AT | 0.00181241 | 0.0300487 | intron-variant | CADPS2 | GRCh38.p7 | 7:122723729 | AAGACACATGCACAC[-/AT]ATGTTTATTGTGGCA | 93664 |
rs529554890 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | CADPS2 | GRCh38.p7 | 7:122515912 | TTTTGTTAATTTCTT[C/T]ATTAAAAAGTTTAAA | 93664 |
rs529556022 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122659342 | CACCGTGGAAAAAAA[C/T]GAAGAATGCCTTTGA | 93664 |
rs529556524 | snp | C/T | | | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122540314 | AACTTAGTATTATAG[C/T]AATTTAAAAGGAATA | 93664 |
rs529558979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122729798 | AATGGCATGAGTTGC[A/G]CCAACATAATCAGCT | 93664 |
rs529572396 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122523755 | CCCTTCAAAATTTTT[A/G]TCTACACATGCTTCA | 93664 |
rs529576972 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | CADPS2 | GRCh38.p7 | 7:122318780 | TTTTTAAGGCTAGTC[C/T]AGGTACCTAACGACC | 93664 |
rs529578145 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122357954 | TTTGTGCATAGATTT[C/T]GGGGTGGACATATGT | 93664 |
rs529585394 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122855032 | CTTAAAAGCCTTTCT[A/C]CCTGGAGAGGAAGTA | 93664 |
rs529586345 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122567386 | TCTGGCTAGGTTGTT[C/T]GTTTTATTTGTCCTA | 93664 |
rs529586517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122694734 | AATTTATAATCTTTA[C/T]TTTTCATCATTAAGA | 93664 |
rs529591703 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122372832 | CCCAGAGACGTAGAA[A/T]CAGTTAAGTGCATTG | 93664 |
rs529594339 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122521897 | AATCCAAGTTAAGCC[A/T]CAGCTCATATCAGCA | 93664 |
rs529595889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122595149 | TAAAGAGTTAGATGT[A/G]TTATATGAACCAAAA | 93664 |
rs529596122 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122777346 | AGATCCAGTATGGCT[G/T]TTGGAGCTCCAGCTC | 93664 |
rs529605112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122606292 | TGTGAAAGGCAGGCT[A/G]AGAATGAGACTGAGC | 93664 |
rs529612448 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122601990 | GCCATTAACCTTACT[A/G]AATAACTTACTGACA | 93664 |
rs529614921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122457255 | TATCAATGAGGAAGA[C/T]TGCTTAAATATTCAG | 93664 |
rs529620568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122689461 | AAGGGCTGTAACTTG[C/T]ATTTCCTACAGTAAT | 93664 |
rs529622596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122423773 | TGCTTGGCATCATTC[C/T]GAATTTCTGATTCAG | 93664 |
rs529628392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122651623 | GTGTAGTCTTCAGAC[A/G]TGAAGAATTTGAGTG | 93664 |
rs529631957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122353015 | TGCAACAGTGCTTTA[C/T]AATTCAAAGCACATT | 93664 |
rs529637804 | snp | C/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122677190 | AAACCAATATGCCTG[C/T]GGCTTGATAAATACT | 93664 |
rs529639303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122365406 | TTTTGTTGAGGCACA[C/T]CTAGTAGAAGAGCTA | 93664 |
rs529640505 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122392317 | AGTAGTAGTAATTAT[A/C]ATTTACTGGGTGCCT | 93664 |
rs529646998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122456558 | AAGTCAAAAAAGTTA[C/T]GACATAAAACTTCTA | 93664 |
rs529656704 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122646655 | CATGAGAAGGAACAG[C/T]TGAAATGCAGATGGG | 93664 |
rs529660050 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122461841 | CCTGGTGATCCACCC[A/G]CCTCGGCCTCCCAGA | 93664 |
rs529663971 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122361206 | GTCCTTTTCTTTCCC[A/T]TGGCTGGAAATAATA | 93664 |
rs529668296 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122579242 | GACATTTAGCAATGT[A/C]TGGAGACATTTTTTA | 93664 |
rs529681955 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122823259 | AATTTCTCAATTGCA[A/C]AATGCCATTCTATTT | 93664 |
rs529682906 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CADPS2 | GRCh38.p7 | 7:122823768 | GAATAGACCTAACTC[C/T]GAAACCAAGTATCTG | 93664 |
rs529687088 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122555166 | GGAAATCAACTCAAT[G/T]AGAGATGGAAAACAG | 93664 |
rs529691746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122568927 | ACAGCCAATATCATA[C/T]TGAATGGGCAAAAAC | 93664 |
rs529693746 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122560917 | TTAATAACCACATAT[A/C]TTAATATTTGCCCCA | 93664 |
rs529694764 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122404754 | AATAATGCCTCATTT[A/T]AAAATAACCCCCAAA | 93664 |
rs529700693 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122465029 | ATCGTAAAATAAAAA[G/T]TATATCTAAAAAAGA | 93664 |
rs529700756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122721605 | AGCCGAATTCTACCA[A/G]AGGTACAAGGAGGAG | 93664 |
rs529709346 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122726127 | TGCTTTTCCCAATGA[C/T]CTTATGAAAATAAGA | 93664 |
rs529711295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122502680 | GGAATAATTTTTCAT[A/G]TTTAATTGAGCCGCC | 93664 |
rs529715008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122771714 | GGAAGGTGTGGTCAC[A/G]AAGAAAACAAGGCAG | 93664 |
rs529717136 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122865491 | TTCTAAGCCAATTCT[C/T]GCTCCTATTGCAGCA | 93664 |
rs529721137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122548483 | CCTGGTATGTAAATC[C/T]AATGAGATCAACAAT | 93664 |
rs529724013 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122641036 | TGGGGATTGTAATAG[A/G]GATCAGAGGTAAGGC | 93664 |
rs529725001 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122411549 | CTCAAAATATAATAA[A/C]AATTTATAACTTAAA | 93664 |
rs529725775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122411987 | TATTATCCTCATTCA[C/T]ATATATTATAAATCA | 93664 |
rs529737629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122778710 | AGCCTTGGCAGCTTC[C/T]GTGTGGTGTTGAGCC | 93664 |
rs529743744 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122411862 | TCTAACTAATCATAA[C/G]TTTTTTACAACTTCC | 93664 |
rs529749107 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122696629 | TCCAAGGCTGCGCAG[A/C]AATTCAAATCCCAGT | 93664 |
rs529756213 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122655612 | GTGTGAAATAAAAAA[A/T]AATTGTGTGACCTGC | 93664 |
rs529756434 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122404221 | TTGTTCAATTCCCAC[C/G]TATCAGTGAGAATAT | 93664 |
rs529760935 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122371583 | TTATAATTCAAGATG[A/G]GATTTTGGGTGGGAA | 93664 |
rs529760953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122418470 | ATGACTATATCCTAT[A/G]AATAACTTGGGGCAA | 93664 |
rs529775677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122779338 | CTATTCTACTGGTCT[C/T]ATTTTGGATCAGGTG | 93664 |
rs529787603 | snp | G/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122422019 | AATGACTATATATCA[G/T]ATGGATAATGAAAAA | 93664 |
rs529789031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122509757 | GAGTAAGTTCCATAA[C/T]CCCTCTGTATTATTT | 93664 |
rs529795793 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | CADPS2 | GRCh38.p7 | 7:122872372 | TTAAAAACAATGAGA[-/T]TCATTATAGGAACCT | 93664 |
rs529796575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122830853 | TGCAAATCTCTGGTA[C/T]AAAACCATGAAACTA | 93664 |
rs529797913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122659156 | AACTAGATTCAGATA[C/T]GAGACAGATGTTAGA | 93664 |
rs529803021 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122852271 | GGAACTCATTCAATG[C/G]TACCTGAATTCAACT | 93664 |
rs529816608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122567719 | GGTATAATATTGTAA[A/G]GTTCTTAAATATACA | 93664 |
rs529823898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122518094 | TGCTCCACTAGGCAA[C/T]AGATTTTGTTCATTA | 93664 |
rs529826038 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122573947 | TCTTCTATTGCACTG[C/G]GTTACTTTTGAACAG | 93664 |
rs529831594 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122874999 | CAAAACAGAAAATAA[A/G/T]ATTAAACATATCAGT | 93664 |
rs529831842 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122732127 | CCCCACCCAAGAAAA[A/C]ACCACATAGAAATAC | 93664 |
rs529833591 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122646276 | AACATTACTGTACAT[A/T]TGGTACAACAGTACA | 93664 |
rs529835507 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122624847 | ACCATGAAGATAATG[A/G]ACAAAGTCCTGATAG | 93664 |
rs529839888 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122344514 | TTAGGCATTGTCATG[A/C]CTAAATGAAGACCTT | 93664 |
rs529840833 | snp | A/C | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122854256 | GTAGTCCCAGCTTCC[A/C]AGCTACTTGGGAAGC | 93664 |
rs529848574 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122840990 | AAATGCTTAAACTGA[A/G]CAAGAGTTTATGTAA | 93664 |
rs529856582 | snp | C/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122871940 | TCTCCTTGCTAGACT[C/G]TCTTTTCTTGGGCTT | 93664 |
rs529863307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122368074 | TTATCTCACAGGGTT[C/T]TGCCATGTTGGCCAG | 93664 |
rs529876383 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122740413 | AAGACATGGAGGAAC[C/G]TTAAATGCATATTAC | 93664 |
rs529894824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122525882 | GAATTGTAACACAAT[A/G]GCAAGTATTTGTGTT | 93664 |
rs529904302 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122726096 | ATTCACCCATCTGGA[A/T]TCAGAGGCAAAAGAA | 93664 |
rs529905471 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122754697 | GCCAGGTTGGTCTCA[A/C]ACTCCTGACTCAGGG | 93664 |
rs529913009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122627662 | AAATCACTTAAACTT[C/T]ATTCTAAAGCATTAC | 93664 |
rs529913215 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122747078 | ACCAATTATCACAAA[C/G/T]AGCAGCCTGAGTGAT | 93664 |
rs529923912 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122444892 | ACACAGATTTTTCAC[C/T]CAAGTTTTCTAGGTC | 93664 |
rs529930668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122696142 | ACATTAACAGTGGCC[A/G]AAGAATGACAATTTA | 93664 |
rs529933066 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122480008 | AACTGAGAGACAGTG[A/C]AAACCAGGGTGTGTG | 93664 |
rs529937051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122373938 | CCTGATACCAAAGCC[A/G]GACAAAAGATACTGC | 93664 |
rs529939378 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CADPS2 | GRCh38.p7 | 7:122722027 | CAATAAATTTGGTAT[C/T]GATGGGACATATCTC | 93664 |
rs529953525 | in-del | -/TTTT | 0.0244538 | 0.107838 | intron-variant | CADPS2 | GRCh38.p7 | 7:122442785 | ATCTAGTCACTCAAG[-/TTTT]TTTTTTAACAGAATA | 93664 |
rs529956224 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CADPS2 | GRCh38.p7 | 7:122432149 | GTCTTGGAGGCATGG[C/T]AGCCAGTGAAAAGAA | 93664 |
rs529964619 | snp | A/G | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122693494 | CTGGCAGTGGTTCTC[A/G]GTCTTGTGTGCACAC | 93664 |
rs529965103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122650815 | CTTAATTCTACCAGA[A/G]ACTCAAATTCATTTT | 93664 |
rs529967873 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122620383 | TTTATCTTAATGCCT[C/G]ACATAAGTTCTTTCT | 93664 |
rs529969436 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122486678 | TAAAGTTTTAGAGGA[C/T]TGACTCCAATTTTCA | 93664 |
rs529971237 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122479141 | GGGAGTGGGACTCTA[G/T]TATCAAAAGGACTAA | 93664 |
rs529973684 | snp | C/T | 1.65627e-05 | 0.00287769 | intron-variant, missense | CADPS2, RNF148 | GRCh38.p7 | 7:122702284 | ATGCCTTTCAGGTTG[C/T]TTATCATCACCGCGA | 93664 |
rs529974538 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122848739 | TATCTTGCATCTGTG[G/T]GTAAAATGCCATGAC | 93664 |
rs529977987 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122708746 | TACATAACTTTAACA[A/G]TAAATTGAAAACAAT | 93664 |
rs529978759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122380743 | ATTAACCACACTGAT[A/G]TGAATGTGGAATTTT | 93664 |
rs529980461 | snp | C/T | | | intron-variant, nc-transcript-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122530599 | AACAATCTTATAAGG[C/T]TTCAATTATCACTAC | 93664 |
rs529982902 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122581069 | TAACAAATTATTTTA[C/T]GTAATTTATGAACAT | 93664 |
rs529985089 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CADPS2, LOC105375481 | GRCh38.p7 | 7:122532794 | ATTTCCCGAGAGTAC[A/G]ATAAACAATTTTAAT | 93664 |
rs529986479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122525190 | AATTTTGATCATAAT[C/T]TCCATGGACTATACT | 93664 |
rs530005210 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122747871 | CTGCCTAGAATACCA[C/T]AGAACCTAATTAAGA | 93664 |
rs530007752 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122798222 | CAAGAGAGGAAAAGG[G/T]GCTGTGATCGTCCCT | 93664 |
rs530012465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122837318 | CTAAATGCCCACAAG[A/G]GAAAGCAGGAAAGAT | 93664 |
rs530018458 | snp | A/T | | | intron-variant | CADPS2 | GRCh38.p7 | 7:122662441 | AGTGCAGTGGCACGA[A/T]CTCAGCTCACTGCAA | 93664 |
rs530022746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122613788 | TATACTGTGACTAGG[C/T]CACAAAAGTAAGTTT | 93664 |
rs530028155 | snp | C/T | 0.332799 | 0.23589 | intron-variant | CADPS2 | GRCh38.p7 | 7:122569565 | CCAAAAAAGAGCCTG[C/T]ATTGCCAAGACAATC | 93664 |
rs530033799 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CADPS2 | GRCh38.p7 | 7:122742252 | ATACAAAAATTAGCC[G/T]GGTGTGGTGGCATGT | 93664 |
rs530037531 | snp | C/T | 1.66037e-05 | 0.00288125 | intron-variant, synonymous-codon | CADPS2, RNF148 | GRCh38.p7 | 7:122702577 | CCCGAACACTCCACT[C/T]TCTCCTAATTCCGAT | 93664 |
rs530043005 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CADPS2 | GRCh38.p7 | 7:122473735 | TCCCCATATTCTGAG[A/G]TGTCAAGCATTCCTT | 93664 |
rs530055986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CADPS2 | GRCh38.p7 | 7:122841574 | GAAAACTGAGCATTT[C/T]TTAGGTTTCTGTAAA | 93664 |