SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs706763 | snp | A/G | 0.110102 | 0.207195 | synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749581 | GAGTTCCTGGCGTCC[A/G]CAGAAGGTCTGAATG | 284434 |
rs706764 | snp | C/T | 0.0115846 | 0.0752203 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749294 | GGTTCTGGGCATCAG[C/T]GTCCAGGCAGCCATC | 284434 |
rs773835 | snp | A/G | 0.160167 | 0.233307 | intron-variant | NWD1 | GRCh38.p7 | 19:16773101 | AGGGATGTAGACTAA[A/G]TTGCCTGGATTGAGC | 284434 |
rs773836 | snp | A/T | 0.316726 | 0.240931 | intron-variant | NWD1 | GRCh38.p7 | 19:16772140 | gggctcaagatatcc[A/T]ccttcctcgacccct | 284434 |
rs773837 | snp | A/C | 0.316 | 0.241131 | intron-variant | NWD1 | GRCh38.p7 | 19:16771610 | TAAATCTTCCTTAAA[A/C]TGGGAAGTCATGCCC | 284434 |
rs773838 | snp | C/T | 0.244205 | 0.249933 | intron-variant | NWD1 | GRCh38.p7 | 19:16771321 | ctgggattacaggca[C/T]gcaccaccacacccg | 284434 |
rs773839 | snp | C/G | 0.495291 | 0.0482933 | intron-variant | NWD1 | GRCh38.p7 | 19:16770553 | cgccaagatttcaat[C/G]gacacggtggggctc | 284434 |
rs773840 | snp | C/T | 0.315758 | 0.241197 | intron-variant | NWD1 | GRCh38.p7 | 19:16770162 | aattcaagatgatag[C/T]tgggtggggacacag | 284434 |
rs773841 | snp | C/T | 0.495483 | 0.0473088 | intron-variant | NWD1 | GRCh38.p7 | 19:16768895 | AAGAGAAGCAGATAG[C/T]TCAAGGATGGTTTGC | 284434 |
rs773842 | snp | A/G | 0.171704 | 0.237423 | intron-variant | NWD1 | GRCh38.p7 | 19:16759115 | CGCGGTGTCCAGCAC[A/G]TCACCTGGGATCAGC | 284434 |
rs773843 | snp | C/T | 0.16976 | 0.236773 | intron-variant | NWD1 | GRCh38.p7 | 19:16758849 | ggctaatttttgcat[C/T]tttagtagagacggg | 284434 |
rs773844 | snp | C/T | 0.462034 | 0.132445 | intron-variant | NWD1 | GRCh38.p7 | 19:16758449 | ctctacaaaaaaatt[C/T]aaaaattagctgggc | 284434 |
rs773845 | snp | A/G | 0.495927 | 0.0449436 | intron-variant | NWD1 | GRCh38.p7 | 19:16758152 | tgagttgtgtgaagc[A/G]cctttcaagtgttcc | 284434 |
rs773846 | snp | C/G | 0.495927 | 0.0449436 | intron-variant | NWD1 | GRCh38.p7 | 19:16758073 | AACACTGTACTCTTT[C/G]CAAAAttcttttttt | 284434 |
rs773847 | snp | C/G | 0.495445 | 0.0475058 | intron-variant | NWD1 | GRCh38.p7 | 19:16757744 | TGATATGGTATCAGA[C/G]AGAGCCTAGGAGATG | 284434 |
rs773848 | snp | A/T | 0.17138 | 0.237316 | intron-variant | NWD1 | GRCh38.p7 | 19:16757671 | TCATCCCTGAAGACA[A/T]CCCCTAAGCAATGCG | 284434 |
rs773849 | snp | A/G | 0.495521 | 0.0471118 | intron-variant | NWD1 | GRCh38.p7 | 19:16757162 | cccgcggaccagggt[A/G]ggggtgatggttttg | 284434 |
rs773850 | snp | C/G | 0.166506 | 0.235645 | intron-variant | NWD1 | GRCh38.p7 | 19:16755971 | aaggcttctggtcaa[C/G]agtaggctattagta | 284434 |
rs773851 | snp | C/T | 0.164546 | 0.234942 | intron-variant | NWD1 | GRCh38.p7 | 19:16762925 | gcagtggcacacacc[C/T]gtagtcccaggtact | 284434 |
rs773852 | snp | C/T | 0.472718 | 0.113564 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16762129 | CCTCACCTTTCGGTC[C/T]AAGTTCAGTGGTTTC | 284434 |
rs773889 | snp | C/T | 0.136166 | 0.22258 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815856 | GATCAGATGACAGCA[C/T]CTACAGCTTTATAAA | 284434 |
rs773890 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | NWD1 | GRCh38.p7 | 19:16814862 | CCTTTATCTGCACAA[C/T]GGGAATGATAACAGA | 284434 |
rs773891 | snp | G/T | 0.0599851 | 0.162463 | intron-variant | NWD1 | GRCh38.p7 | 19:16814118 | ggctggagtgcaatg[G/T]tgctatcatggctca | 284434 |
rs773892 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | NWD1 | GRCh38.p7 | 19:16814030 | gctgggactacaagc[A/G]tgtaccaccatgcct | 284434 |
rs773893 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | NWD1 | GRCh38.p7 | 19:16813714 | cgaggtgggtggatc[A/G]cccaaggtcaggagt | 284434 |
rs773894 | snp | C/G | 0.496778 | 0.0400063 | intron-variant | NWD1 | GRCh38.p7 | 19:16812683 | tttgtttgtttgttt[C/G]tttgtttgtttttga | 284434 |
rs773913 | snp | C/T | 0.168135 | 0.236216 | intron-variant | NWD1 | GRCh38.p7 | 19:16751093 | gggattacaggcatg[C/T]accaccacgcctggc | 284434 |
rs773914 | snp | A/C | 0.204496 | 0.245824 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748841 | ACTCTTAttcttctt[A/C]ttattattattatta | 284434 |
rs773915 | snp | A/G | 0.16618 | 0.23553 | intron-variant | NWD1 | GRCh38.p7 | 19:16747448 | tggaggccacactga[A/G]ccgtgatcgtgccac | 284434 |
rs773916 | snp | A/G | 0.215144 | 0.247558 | intron-variant | NWD1 | GRCh38.p7 | 19:16746053 | atttatgtgattggt[A/G]ggctattagtagtta | 284434 |
rs773917 | snp | G/T | 0.460252 | 0.135255 | intron-variant | NWD1 | GRCh38.p7 | 19:16745481 | tcggccttccaaaat[G/T]ctgggattacaggta | 284434 |
rs773918 | snp | A/G | 0.383053 | 0.211653 | intron-variant | NWD1 | GRCh38.p7 | 19:16743775 | gaattgcttgaaccc[A/G]ggagagggaggtttc | 284434 |
rs773919 | snp | A/T | 0.4776 | 0.103433 | intron-variant | NWD1 | GRCh38.p7 | 19:16743675 | aataaataaacaaac[A/T]aataaataaataaat | 284434 |
rs773925 | snp | C/T | 0.1652 | 0.235179 | intron-variant | NWD1 | GRCh38.p7 | 19:16781351 | tgggataagccacca[C/T]gcccagccAACTGTA | 284434 |
rs773926 | snp | A/G | 0.1652 | 0.235179 | intron-variant | NWD1 | GRCh38.p7 | 19:16781189 | TTCCATCCTAGTCCC[A/G]ACCCTCGTCTGTCTC | 284434 |
rs773927 | snp | A/G | 0.1652 | 0.235179 | intron-variant | NWD1 | GRCh38.p7 | 19:16781178 | TCCCAACCCTCGTCT[A/G]TCTCTCTTCAGCATC | 284434 |
rs773928 | snp | A/G | 0.362523 | 0.223246 | intron-variant | NWD1 | GRCh38.p7 | 19:16780662 | agaaaaaaagaatga[A/G]aaaaagaaaaggaaa | 284434 |
rs773929 | snp | A/G | 0.16618 | 0.23553 | intron-variant | NWD1 | GRCh38.p7 | 19:16779946 | CAATGCACAGGAAGT[A/G]AGCTAAAGAAATAGC | 284434 |
rs773930 | snp | C/G | 0.15522 | 0.231337 | missense | NWD1 | GRCh38.p7 | 19:16779432 | TGTGGATCACATGCT[C/G]CTCTTCCATGTCCCA | 284434 |
rs773931 | snp | A/C | 0.365853 | 0.221536 | intron-variant | NWD1 | GRCh38.p7 | 19:16778509 | caacaacaacaacaa[A/C]aaaaaaaaaaaaaaa | 284434 |
rs796480 | snp | C/G | 0.318896 | 0.240319 | intron-variant | NWD1 | GRCh38.p7 | 19:16772507 | aggtgcccgccacca[C/G]gcccaactaattttt | 284434 |
rs796482 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16778791 | gcactttgggaggcc[A/G]atactttgggaggCC | 284434 |
rs810149 | snp | G/T | 0.304188 | 0.244057 | intron-variant | NWD1 | GRCh38.p7 | 19:16778801 | atgccacccagcact[G/T]tgggaggccgatact | 284434 |
rs811791 | snp | C/T | 0.487995 | 0.0765403 | intron-variant | NWD1 | GRCh38.p7 | 19:16764365 | ggatggatggatgga[C/T]ggacagaagatgggt | 284434 |
rs812847 | snp | C/T | 0.493726 | 0.0556554 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744454 | CGATCCGCGAGGGAA[C/T]CAGACAGGGGCCGTA | 284434 |
rs878506 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | NWD1 | GRCh38.p7 | 19:16739724 | TGGTAAATAAGTCAT[C/T]AGGCAGCACCGAGGC | 284434 |
rs878507 | snp | A/G | 0.486725 | 0.0803809 | intron-variant | NWD1 | GRCh38.p7 | 19:16739922 | CCACCTGTTTCCTTC[A/G]TATAACCTCTGGTCT | 284434 |
rs1082126 | snp | C/G | 0.495483 | 0.0473088 | intron-variant | NWD1 | GRCh38.p7 | 19:16768740 | TCCTTTGTGAATTCA[C/G]CTCACAATTTATTGC | 284434 |
rs2248743 | snp | C/T | 0.172028 | 0.23753 | intron-variant | NWD1 | GRCh38.p7 | 19:16798431 | gtagagattgggtct[C/T]gctatgttgcccagg | 284434 |
rs2313249 | snp | A/C | 0.208169 | 0.246476 | intron-variant | NWD1 | GRCh38.p7 | 19:16752218 | GAGAAAAAAAAAAAA[A/C]AACCCTAAAACTGAG | 284434 |
rs2361631 | snp | C/T | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16799184 | aaataaataagaaaa[C/T]AAGAAATACACTTCA | 284434 |
rs2431801 | snp | A/T | 0.355525 | 0.226637 | intron-variant | NWD1 | GRCh38.p7 | 19:16794716 | TCTTTGCAACTGAGG[A/T]TGTCTCGTCTGGACT | 284434 |
rs2431802 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | NWD1 | GRCh38.p7 | 19:16794663 | CCATTTGGCAGAAAA[A/C]GTTGCTAACCTCTGG | 284434 |
rs2446148 | snp | A/G | 0.494442 | 0.0524218 | intron-variant | NWD1 | GRCh38.p7 | 19:16790067 | CTGAAAACAATGTCT[A/G]TTCCACTGTGTTATT | 284434 |
rs2446149 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764422 | atcatagatggatgg[A/G]tggataaatggatag | 284434 |
rs2446150 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764416 | gatggatgggtggat[A/G]aatggatagttagat | 284434 |
rs2446151 | snp | A/G | 0.152334 | 0.230133 | intron-variant | NWD1 | GRCh38.p7 | 19:16764415 | atggatgggtggata[A/G]atggatagttagatg | 284434 |
rs2547088 | snp | A/G | 0.317933 | 0.240593 | | | GRCh38.p7 | 19:16775389 | CAAAAGCAGAGGCAA[A/G]AGGGAGTCTTTAGGG | 284434 |
rs2547102 | snp | C/T | 0.00279162 | 0.0372561 | | | GRCh38.p7 | 19:16818327 | GATTGCTGAGCTTTT[C/T]GGCATCCCTTAATTT | 284434 |
rs2547103 | snp | A/G | 0.0287284 | 0.116357 | | | GRCh38.p7 | 19:16809647 | gaatggcataaaccc[A/G]ggaggcagagcttgt | 284434 |
rs2547104 | snp | A/G | 0.223225 | 0.248562 | | | GRCh38.p7 | 19:16804554 | aggctggagtgcagt[A/G]gcattatcatagctc | 284434 |
rs2547105 | snp | A/C | 0.494429 | 0.052484 | | | GRCh38.p7 | 19:16794800 | AGCAAGACCCTATTT[A/C]AAAAAAAAAGAAAAA | 284434 |
rs2547106 | snp | A/G | 0.225005 | 0.248747 | | | GRCh38.p7 | 19:16786854 | accctgcccagcctg[A/G]gattacttttataag | 284434 |
rs2547107 | snp | A/G | 0.213937 | 0.247385 | | | GRCh38.p7 | 19:16786894 | cccattccccagagc[A/G]ccatcctcataacct | 284434 |
rs2547108 | snp | A/G | 0.367297 | 0.220775 | | | GRCh38.p7 | 19:16788920 | GCTGACAAGCATTTT[A/G]ATAGTTGCAAGGCCA | 284434 |
rs2547109 | snp | A/T | 0.00716266 | 0.059414 | | | GRCh38.p7 | 19:16791844 | CTCAGCCTTCCGAGT[A/T]GCTGGGATTACAGGC | 284434 |
rs2547113 | snp | C/T | 0.313082 | 0.241911 | | | GRCh38.p7 | 19:16765704 | AAGAAAAGTCCAGGG[C/T]AACAGGATGGGCCCT | 284434 |
rs2608723 | snp | C/T | 0.319616 | 0.240112 | | | GRCh38.p7 | 19:16806084 | GGAGTTTGAGACCAG[C/T]CTGGCCAACATGGCA | 284434 |
rs2608724 | snp | A/G | 0.260227 | 0.249791 | | | GRCh38.p7 | 19:16805876 | ctctcaaaaaaaaaa[A/G]aagaaaagaaagaaa | 284434 |
rs2608725 | snp | A/G | 0.223522 | 0.248594 | | | GRCh38.p7 | 19:16804141 | TCAACCCTTTCCCCC[A/G]CCAGCCCCATTTTCT | 284434 |
rs2608726 | snp | A/T | 0.493703 | 0.0557558 | | | GRCh38.p7 | 19:16801862 | gagaactaacagagt[A/T]agaacttactcacca | 284434 |
rs2608727 | snp | C/T | 0.356597 | 0.226135 | | | GRCh38.p7 | 19:16801589 | agcttggactacaga[C/T]gtgagccactacacc | 284434 |
rs2608729 | snp | A/G | 0.180383 | 0.240111 | | | GRCh38.p7 | 19:16794290 | caacctccgcctccc[A/G]ggttcaagcaattcc | 284434 |
rs2608730 | snp | A/G | 0.313082 | 0.241911 | | | GRCh38.p7 | 19:16766522 | ATGGCCAGAGCGTCT[A/G]AAGACTTGGAGAGAT | 284434 |
rs2608731 | snp | C/T | 0.166506 | 0.235645 | | | GRCh38.p7 | 19:16765690 | GCAACAGGATGGGCC[C/T]TGCTTTGGTAGTATT | 284434 |
rs2608736 | snp | C/T | 0.225005 | 0.248747 | | | GRCh38.p7 | 19:16786635 | cactgcaacctctgc[C/T]tcccaggttcaagcg | 284434 |
rs2608737 | snp | A/T | 0.000708081 | 0.0188026 | | | GRCh38.p7 | 19:16789027 | AAGGGACCCTCGCCA[A/T]CTCTGCTTCAAAGGA | 284434 |
rs2608738 | snp | A/G | 0.168574 | 0.236368 | | | GRCh38.p7 | 19:16789054 | AGGATTACACGCTGC[A/G]CTTGTGGAACTTACT | 284434 |
rs2608739 | snp | C/T | 0.228547 | 0.249078 | | | GRCh38.p7 | 19:16809585 | TTTGAGATGGAGTCT[C/T]GCTCTGTCACCCAGG | 284434 |
rs2608741 | snp | C/G | 0.0399052 | 0.1355 | | | GRCh38.p7 | 19:16810332 | AATCCCGGCTACCCG[C/G]GAGGCCGAGGCAGGA | 284434 |
rs2608742 | snp | A/G | 0.0225045 | 0.103662 | | | GRCh38.p7 | 19:16741565 | CCTGGCCAACATAGC[A/G]AAACCCCATATCTAT | 284434 |
rs2885321 | snp | A/G | 0.172028 | 0.23753 | intron-variant | NWD1 | GRCh38.p7 | 19:16796560 | ataggaatgggtccc[A/G]gtgaaactgtacctt | 284434 |
rs3033488 | in-del | -/TC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751863 | tatctcttctttcct[-/TC]tttttttttctttct | 284434 |
rs3745320 | snp | A/G | | | missense | NWD1 | GRCh38.p7 | 19:16807726 | CAGGACGTGATATGC[A/G]TTCCCCCTCCCGAGG | 284434 |
rs3745321 | snp | A/G | 0.0139748 | 0.0824142 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807851 | CGGGGACCCCTGCCC[A/G]GTCATCGATGGGCCA | 284434 |
rs3848654 | snp | A/G | 0.483563 | 0.0891524 | intron-variant | NWD1 | GRCh38.p7 | 19:16745204 | tgaataagtctcaca[A/G]gatctgatggtttta | 284434 |
rs3848655 | snp | C/T | 0.0980852 | 0.198549 | intron-variant | NWD1 | GRCh38.p7 | 19:16745225 | cccatactgttctcg[C/T]ggtagtgaataagtc | 284434 |
rs3888834 | snp | A/G | 1.7159e-05 | 0.00292903 | missense, upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749162 | TGGGAGATAGAGCGG[A/G]GCCTGCTGAGCTCAG | 284434 |
rs4490105 | snp | A/G | 0.391954 | 0.205789 | intron-variant | NWD1 | GRCh38.p7 | 19:16803151 | catcagatctcatga[A/G]acttattcgctacca | 284434 |
rs4563153 | snp | C/T | 0.39214 | 0.205661 | intron-variant | NWD1 | GRCh38.p7 | 19:16802374 | tggaggcaggatgat[C/T]gcttgagcccaggaa | 284434 |
rs4808055 | snp | C/T | 0.286042 | 0.247388 | intron-variant | NWD1 | GRCh38.p7 | 19:16802410 | ggctgcagtgaactg[C/T]gattgcaccactgca | 284434 |
rs4808524 | snp | A/T | 0.483852 | 0.0883933 | intron-variant | NWD1 | GRCh38.p7 | 19:16720567 | tctagggagactttt[A/T]tttttttgagacgga | 284434 |
rs4808525 | snp | C/G | 0.467845 | 0.122652 | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16721395 | TCCTGCGATCATCAG[C/G]AGGCAGTAACCAAGG | 284434 |
rs4808526 | snp | C/T | 0.202035 | 0.245356 | intron-variant | NWD1 | GRCh38.p7 | 19:16765288 | CTGGATTTTCATCAA[C/T]TCTCATACCTTTCCT | 284434 |
rs5827343 | in-del | -/AAG | 0.0930568 | 0.194599 | intron-variant | NWD1 | GRCh38.p7 | 19:16751864 | GAAAGAAAAAAAAAG[-/AAG]GAAAGAAGAGATAAA | 284434 |
rs6512135 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | NWD1 | GRCh38.p7 | 19:16789368 | CATAGTTGGATTAGA[C/T]AATCCTGATAATTCT | 284434 |
rs7245422 | snp | C/T | 0.104504 | 0.2033 | intron-variant | NWD1 | GRCh38.p7 | 19:16804518 | gaggattgcttgagc[C/T]gtggagttcaaggct | 284434 |
rs7246439 | snp | C/T | 0.139225 | 0.224118 | intron-variant | NWD1 | GRCh38.p7 | 19:16725834 | gtgggattacaggca[C/T]gTgattgtagctcac | 284434 |
rs7246714 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NWD1 | GRCh38.p7 | 19:16726086 | tcctgcctcagcctc[C/T]ggagtagctaggatt | 284434 |
rs7246962 | snp | A/C | 0.163564 | 0.234582 | intron-variant | NWD1 | GRCh38.p7 | 19:16746676 | gactctgtctaaaaa[A/C]aaaaaacaaaaaaca | 284434 |
rs7247028 | snp | A/G | 0.478411 | 0.101628 | intron-variant | NWD1 | GRCh38.p7 | 19:16745179 | gccaagcgaaagggg[A/G]aattccttataaaac | 284434 |
rs7247204 | snp | C/T | 0.497558 | 0.0348586 | intron-variant | NWD1 | GRCh38.p7 | 19:16732433 | CTTCCTGGCCCTCTT[C/T]GTACTGGGCTTCAGG | 284434 |
rs7248270 | snp | C/T | 0.089084 | 0.191327 | intron-variant | NWD1 | GRCh38.p7 | 19:16801904 | aaaaagaacctgacC[C/T]CAGCTACTCAggagg | 284434 |
rs7249312 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | NWD1 | GRCh38.p7 | 19:16760110 | cactgagccgtgact[A/G]taccactgcactcca | 284434 |
rs7249526 | snp | C/T | 0.156319 | 0.231784 | intron-variant | NWD1 | GRCh38.p7 | 19:16811323 | GCACAGTGGCTCATG[C/T]CTGTAATCCTAGCAC | 284434 |
rs7250172 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | NWD1 | GRCh38.p7 | 19:16760128 | ccactgcactccagt[C/T]tgggtgacagagtga | 284434 |
rs7250251 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NWD1 | GRCh38.p7 | 19:16798708 | ctcagctcactgcaa[C/T]ctcgacctcctgggt | 284434 |
rs7250382 | snp | C/T | 0.0193772 | 0.0965046 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16719426 | acaggcatgagccac[C/T]gtgcccggtcTTGGA | 284434 |
rs7250854 | snp | C/T | 0.0193772 | 0.0965046 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16719193 | caggctgcagtgcag[C/T]ggcaggatctcggct | 284434 |
rs7251510 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | NWD1 | GRCh38.p7 | 19:16754800 | ctctatcatccatcc[A/G]tccatccatccatcc | 284434 |
rs7253335 | snp | A/G | 0.0952156 | 0.196321 | intron-variant | NWD1 | GRCh38.p7 | 19:16760911 | ttaaagttgacaatt[A/G]agtggtattttagta | 284434 |
rs7255230 | snp | C/T | 0.0818113 | 0.184966 | intron-variant | NWD1 | GRCh38.p7 | 19:16755124 | tcatctctatttcta[C/T]ccatctagtcattta | 284434 |
rs7257012 | snp | A/G | 0.0973687 | 0.197999 | intron-variant | NWD1 | GRCh38.p7 | 19:16752892 | tagtcccagctactc[A/G]ggaggctgaggcagg | 284434 |
rs7257182 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16803770 | taaaaaaaaaaaaaa[A/G]aaaaattatctgggc | 284434 |
rs7258021 | snp | C/T | 0.0948562 | 0.196037 | intron-variant | NWD1 | GRCh38.p7 | 19:16760896 | tgcccagtcAGAatt[C/T]taaagttgacaattg | 284434 |
rs7258145 | snp | C/T | 0.0973687 | 0.197999 | intron-variant | NWD1 | GRCh38.p7 | 19:16753120 | TCATAAAAATCAGAG[C/T]AGCTTCTCCTTCCTT | 284434 |
rs7351052 | snp | C/T | 0.0901694 | 0.192235 | intron-variant | NWD1 | GRCh38.p7 | 19:16797555 | ggttcaccatgttgg[C/T]caggctgatctcgaa | 284434 |
rs8100178 | snp | A/G | 0.0930568 | 0.194599 | intron-variant | NWD1 | GRCh38.p7 | 19:16758628 | AGGGTGGAGTGGGGT[A/G]GGTGCAGTTGGTTTC | 284434 |
rs8100417 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16725014 | tttttatttattttt[A/T]atttttttatttttt | 284434 |
rs8100421 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16725022 | tattttttatttttt[A/T]attttttgagacggg | 284434 |
rs8100492 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | NWD1 | GRCh38.p7 | 19:16737054 | ACCCCCTCCACTTTA[G/T]GTCTATAGAACTTTG | 284434 |
rs8100890 | snp | C/T | 0.49607 | 0.0441545 | intron-variant | NWD1 | GRCh38.p7 | 19:16768068 | acgatctcagctcac[C/T]gcaacctccacctcc | 284434 |
rs8101218 | snp | C/T | 0.499987 | 0.00259581 | intron-variant | NWD1 | GRCh38.p7 | 19:16731689 | agctcactgcaacct[C/T]ggcctccagggttca | 284434 |
rs8101228 | snp | C/T | 0.49999 | 0.00219646 | intron-variant | NWD1 | GRCh38.p7 | 19:16731715 | gttcaagcgattctc[C/T]cgcctcagcctcctg | 284434 |
rs8101256 | snp | G/T | 0.499984 | 0.00279548 | intron-variant | NWD1 | GRCh38.p7 | 19:16731767 | ccgccaccacgcccc[G/T]ctaTCCATACTCTTT | 284434 |
rs8102441 | snp | C/T | 0.496968 | 0.0388195 | intron-variant | NWD1 | GRCh38.p7 | 19:16733291 | tttgggaggccaagg[C/T]gggtagatcacctga | 284434 |
rs8103361 | snp | A/G | 0.486266 | 0.0817214 | intron-variant | NWD1 | GRCh38.p7 | 19:16738448 | gtggcacatgcctgt[A/G]atcccagctacttgg | 284434 |
rs8104526 | snp | A/C | 0.495521 | 0.0471118 | intron-variant | NWD1 | GRCh38.p7 | 19:16768462 | cactagatcacatgg[A/C]aattttgtgtttaac | 284434 |
rs8106023 | snp | C/T | 0.0883596 | 0.190715 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816984 | agtaactgtggtttt[C/T]gccattaaaaatatt | 284434 |
rs8107776 | snp | G/T | 0.496542 | 0.041439 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16731241 | TGCCTACCCTGAAGT[G/T]CCAGACCTTCTGCCA | 284434 |
rs8107871 | snp | C/G | 0.00835701 | 0.0640989 | intron-variant | NWD1 | GRCh38.p7 | 19:16731299 | TGGAAGTCACTCCGG[C/G]CTCCATGCttttttt | 284434 |
rs8108084 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790638 | aagtaacattaaaaa[A/T]aaataaataaataaa | 284434 |
rs8108201 | snp | C/T | 0.14933 | 0.228835 | intron-variant | NWD1 | GRCh38.p7 | 19:16799528 | ttattttttttgaga[C/T]ggagtttcattcttg | 284434 |
rs8108763 | snp | A/G | 0.388775 | 0.207946 | intron-variant | NWD1 | GRCh38.p7 | 19:16731020 | aggcagaggagagag[A/G]atctcttgaggccag | 284434 |
rs8109413 | snp | A/G | 0.491051 | 0.0662916 | intron-variant | NWD1 | GRCh38.p7 | 19:16720845 | ggcgtgagccaccgc[A/G]cctggccgagacttt | 284434 |
rs8109655 | snp | A/G | 0.084728 | 0.187577 | intron-variant | NWD1 | GRCh38.p7 | 19:16796765 | ATCatagttatcaaa[A/G]gcctgctgtgtgccc | 284434 |
rs8110046 | snp | A/G | 0.203882 | 0.245709 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749008 | cgagacccccaggtc[A/G]gactctggtgcacgt | 284434 |
rs8110060 | snp | C/G | 0.246485 | 0.249975 | intron-variant | NWD1 | GRCh38.p7 | 19:16744089 | atatattgaattgga[C/G]aaagaatagtaaatt | 284434 |
rs8110650 | snp | C/T | 0.246769 | 0.249979 | intron-variant | NWD1 | GRCh38.p7 | 19:16743929 | ctcaggtaatccacc[C/T]gccttggcctcccaa | 284434 |
rs8110657 | snp | A/G | 0.0948562 | 0.196037 | intron-variant | NWD1 | GRCh38.p7 | 19:16761514 | agagcacaccaccac[A/G]cccagctaatttttg | 284434 |
rs8110726 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16812628 | gagctgagatcacac[C/G]actgcactccagcct | 284434 |
rs8110906 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16812221 | gttgaggcaggagga[C/T]agcttgaaaccagga | 284434 |
rs8111063 | snp | A/G | 0.499982 | 0.00299515 | intron-variant | NWD1 | GRCh38.p7 | 19:16731754 | ggattacaggtgccc[A/G]ccaccacgcccCTCT | 284434 |
rs8111360 | snp | A/T | 0.245916 | 0.249967 | intron-variant | NWD1 | GRCh38.p7 | 19:16744130 | acagtggctcacgac[A/T]gtaatcccagcactt | 284434 |
rs8111480 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16725015 | ttttatttatttttt[A/T]tttttttattttttg | 284434 |
rs8111484 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16725023 | attttttattttttt[A/T]ttttttgagacgggg | 284434 |
rs8111486 | snp | C/T | 0.336474 | 0.234568 | intron-variant | NWD1 | GRCh38.p7 | 19:16760894 | tgtgcccagtcAGAa[C/T]tttaaagttgacaat | 284434 |
rs8111579 | snp | C/T | 0.499923 | 0.00618962 | intron-variant | NWD1 | GRCh38.p7 | 19:16731451 | agctgggactacagg[C/T]gtgcgccaccacgcc | 284434 |
rs8112025 | snp | C/T | 0.49995 | 0.00499176 | intron-variant | NWD1 | GRCh38.p7 | 19:16731854 | ATGTTCTTTTTGCAC[C/T]GAGCCCCGTAGATTC | 284434 |
rs8112102 | snp | A/G | 0.499928 | 0.00598999 | intron-variant | NWD1 | GRCh38.p7 | 19:16731568 | cctcggcctcccaaa[A/G]tgctgggattacagg | 284434 |
rs8112199 | snp | A/G | 0.499992 | 0.00199679 | intron-variant | NWD1 | GRCh38.p7 | 19:16731601 | tgagccactgagccc[A/G]gccCCATGCtttttt | 284434 |
rs8112399 | snp | C/T | 0.490997 | 0.0664859 | intron-variant | NWD1 | GRCh38.p7 | 19:16720848 | gtgagccaccgcacc[C/T]ggccgagactttttc | 284434 |
rs8112538 | snp | G/T | 0.497776 | 0.0332724 | intron-variant | NWD1 | GRCh38.p7 | 19:16810049 | caaaaggattttttt[G/T]tgtgtgtgttttgct | 284434 |
rs8113759 | snp | C/T | 0.144296 | 0.226554 | intron-variant | NWD1 | GRCh38.p7 | 19:16796588 | ctatctgcctaggca[C/T]ttgcctgcctcctgc | 284434 |
rs9797686 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16777940 | agggagggaagggaa[A/G]gggaaggaaaggaaa | 284434 |
rs9797687 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16777948 | aagggaaagggaagg[A/G]aaggaaagggaggga | 284434 |
rs9797695 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16778005 | ggggagggaagggaa[A/G]gggaaggaaggggag | 284434 |
rs9797887 | snp | G/T | 0.338976 | 0.23363 | intron-variant | NWD1 | GRCh38.p7 | 19:16778506 | CTTCTTTTTTTTTTT[G/T]TTGTTGTTGTTGTTG | 284434 |
rs10401301 | snp | G/T | 0.0792508 | 0.182605 | intron-variant | NWD1 | GRCh38.p7 | 19:16783591 | gtgagccgagatcgc[G/T]ccactgcactccagc | 284434 |
rs10401409 | snp | A/G | 0.104504 | 0.2033 | intron-variant | NWD1 | GRCh38.p7 | 19:16805328 | cctcccaaagtgcta[A/G]gattacaggtgtgca | 284434 |
rs10402802 | snp | C/T | 0.21303 | 0.247251 | intron-variant | NWD1 | GRCh38.p7 | 19:16783590 | agtgagccgagatcg[C/T]gccactgcactccag | 284434 |
rs10403241 | snp | C/T | 0.0737376 | 0.17729 | intron-variant | NWD1 | GRCh38.p7 | 19:16768135 | gagtagctgggatta[C/T]aggtgtgtgccacca | 284434 |
rs10405874 | snp | C/T | 0.0766824 | 0.180169 | intron-variant | NWD1 | GRCh38.p7 | 19:16779648 | CAAGCCATTTCTTTT[C/T]CTTTTTAAATATGGG | 284434 |
rs10407544 | snp | A/G | 0.0733688 | 0.176922 | intron-variant | NWD1 | GRCh38.p7 | 19:16768389 | acattttgtttatcc[A/G]ttcatctgtctgtgg | 284434 |
rs10408027 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16758957 | tgcagtgagccgaga[C/T]tgcaccactgcactc | 284434 |
rs10409653 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | NWD1 | GRCh38.p7 | 19:16739284 | atcacttgagcccag[A/G]agttcaagaccagct | 284434 |
rs10410132 | snp | C/T | 0.0729998 | 0.176553 | intron-variant | NWD1 | GRCh38.p7 | 19:16768858 | CCTGTGATTCCTATG[C/T]AGAGCTTCTAATCCT | 284434 |
rs10410571 | snp | A/G | 0.0652144 | 0.168387 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816720 | TCCCTTCTCCCCTCC[A/G]TGGAATTCCTGATAG | 284434 |
rs10412190 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16739355 | aaaaaaaaaaaaaaa[A/T]ttatttttttaaGGA | 284434 |
rs10413402 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | NWD1 | GRCh38.p7 | 19:16764349 | atccatccatccatc[C/T]acccatcttctgtcc | 284434 |
rs10414525 | snp | A/C | 0.484138 | 0.0876334 | intron-variant | NWD1 | GRCh38.p7 | 19:16723626 | cCCTTGGCTGATTTT[A/C]ATTTATATCCATTCA | 284434 |
rs10415430 | snp | C/T | 0.0763149 | 0.179815 | intron-variant | NWD1 | GRCh38.p7 | 19:16790009 | AGGCCTGAGCCATCA[C/T]GCCTAGCTTGTTTTA | 284434 |
rs10416226 | snp | A/T | 0.0744748 | 0.178019 | intron-variant | NWD1 | GRCh38.p7 | 19:16782100 | ctctgtctcaaaaaa[A/T]aaaaaaagaaaaaaa | 284434 |
rs10416579 | snp | A/G | 0.490398 | 0.0686206 | intron-variant | NWD1 | GRCh38.p7 | 19:16730568 | aaaatttaaaaaaat[A/G]tatatggctgtggtg | 284434 |
rs10418109 | snp | C/T | | | intron-variant, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800202 | TTTTTGTGGGTAAGG[C/T]TTGGAGCCATCtgtc | 284434 |
rs10418543 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | NWD1 | GRCh38.p7 | 19:16727698 | AGGGTATGGATGGGG[A/G]CTCAGAGGCAGGTTG | 284434 |
rs10420437 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16735159 | cacactctgtgtctc[C/T]taACGTTTTACCTAA | 284434 |
rs10423697 | snp | C/G | | | intron-variant, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800428 | atccccagctacttg[C/G]gaggctgaggcagaa | 284434 |
rs10425680 | snp | C/T | 0.375598 | 0.21616 | intron-variant | NWD1 | GRCh38.p7 | 19:16734612 | aacagggtgtcgctc[C/T]gtcacccaggctgga | 284434 |
rs10427037 | snp | G/T | 0.111928 | 0.208413 | intron-variant | NWD1 | GRCh38.p7 | 19:16725755 | atggggtttcaccat[G/T]ttggccaggctggtc | 284434 |
rs10439170 | snp | C/G | 0.151001 | 0.229563 | intron-variant | NWD1 | GRCh38.p7 | 19:16803623 | TCAATCAGGTGGAAA[C/G]TAGCTAGTCATggcc | 284434 |
rs10439171 | snp | A/G | 0.16846 | 0.236329 | intron-variant | NWD1 | GRCh38.p7 | 19:16803639 | TAGCTAGTCATggcc[A/G]ggtgtggtggctcac | 284434 |
rs10451502 | snp | A/G | 0.499872 | 0.0079862 | intron-variant | NWD1 | GRCh38.p7 | 19:16733026 | CAGGAGTTTGATACC[A/G]GTCTGGGTAATATAA | 284434 |
rs10451503 | snp | A/G | 0.343924 | 0.231686 | intron-variant | NWD1 | GRCh38.p7 | 19:16733046 | gggtaatataacaag[A/G]tcccgtctctataaa | 284434 |
rs10451504 | snp | A/C | 0.343924 | 0.231686 | intron-variant | NWD1 | GRCh38.p7 | 19:16733146 | ggatcacttgaaccc[A/C]ggagtttgaggctgc | 284434 |
rs10451505 | snp | A/G | 0.372189 | 0.218105 | intron-variant | NWD1 | GRCh38.p7 | 19:16733156 | aacccaggagtttga[A/G]gctgcagtgagctgt | 284434 |
rs10451506 | snp | A/C | 0.49949 | 0.0159663 | intron-variant | NWD1 | GRCh38.p7 | 19:16733191 | gagccactgcactct[A/C]gcctgggtgccagat | 284434 |
rs10451507 | snp | A/G | 0.499502 | 0.0157669 | intron-variant | NWD1 | GRCh38.p7 | 19:16733192 | agccactgcactcta[A/G]cctgggtgccagatt | 284434 |
rs10451508 | snp | A/G | 0.343924 | 0.231686 | intron-variant | NWD1 | GRCh38.p7 | 19:16733280 | aatcccagcactttg[A/G]gaggccaaggcgggt | 284434 |
rs10591492 | in-del | -/AAG | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748839 | AATAATAATAATAAT[-/AAG]AAGAAGAATAAGAGT | 284434 |
rs10854153 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | NWD1 | GRCh38.p7 | 19:16721673 | ATGGGGGCGGGGTCC[C/G]TGGAGGAGAGGGGGT | 284434 |
rs11086036 | snp | C/G | 0.0352966 | 0.128072 | intron-variant | NWD1 | GRCh38.p7 | 19:16727592 | CCGAGTACCCGCCGG[C/G]GGCTTCTGCGGGGTG | 284434 |
rs11086037 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16731917 | TAAAAATCCTTGGGA[C/T]TATAAAAAGGCAGGT | 284434 |
rs11291157 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787907 | aataataataataat[A/C]atcatcatcatcatc | 284434 |
rs11292982 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16741369 | TGTTTTGTTTTTGTG[-/T]TTTTTTTTTTTTTTT | 284434 |
rs11307357 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751225 | GCAAAACTCGATCTC[-/A]AAAAAAAAAAAAAAA | 284434 |
rs11307621 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16778495 | TTCTTCTTCTTCTTC[-/T]TTTTTTTTTTTTTGT | 284434 |
rs11334873 | in-del | -/A | 0.103794 | 0.20279 | intron-variant | NWD1 | GRCh38.p7 | 19:16761814 | GTAAGGAAAAAAAAA[-/A]CACGGACCAATTTAG | 284434 |
rs11355024 | in-del | -/T | 0.487305 | 0.0786545 | intron-variant | NWD1 | GRCh38.p7 | 19:16766592 | TACATGTCTTAACCA[-/T]TTTTTTTTTTTGAGA | 284434 |
rs11383216 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16789716 | TCTCTCCTCTCTCTC[-/T]TTTTTTTTTTTTTTT | 284434 |
rs11436280 | in-del | -/A | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16733536 | AAAAAAAAAAAAAAA[-/A]TCAAGTGGCTCTTTG | 284434 |
rs11445714 | in-del | -/T | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16730928 | TTTTTTTTTTTTTTT[-/T]GAGATGGTGGCAGCA | 284434 |
rs11667216 | snp | A/C | 0.151668 | 0.229849 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16747739 | tctcccctctcccag[A/C]gcaggcaaccatcaa | 284434 |
rs11667769 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16730797 | actttgggaggctga[G/T]gtgggaagatggctt | 284434 |
rs11668502 | snp | C/T | 0.087381 | 0.189882 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749273 | AGGATGGTGGACCGG[C/T]TCGCGGATGGCTGCC | 284434 |
rs11669644 | snp | C/T | 0.0763149 | 0.179815 | intron-variant | NWD1 | GRCh38.p7 | 19:16780357 | gagacggggtttcac[C/T]gtgttagccaggatg | 284434 |
rs11670033 | snp | C/G | 0.488485 | 0.0749998 | intron-variant | NWD1 | GRCh38.p7 | 19:16732876 | CAGCTTAACTTGAGG[C/G]CTGCCTCCTTGCTGC | 284434 |
rs11670068 | snp | A/G | 0.499575 | 0.0145705 | intron-variant | NWD1 | GRCh38.p7 | 19:16732890 | GGCTGCCTCCTTGCT[A/G]CTTATGAGAATGATT | 284434 |
rs11670108 | snp | A/G | 0.350764 | 0.228794 | intron-variant | NWD1 | GRCh38.p7 | 19:16733051 | ATATAACAAGATCCC[A/G]TCTCTATAAAATTAA | 284434 |
rs11670247 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16792944 | cagctacttgagagg[C/T]tgatgtgggaggatc | 284434 |
rs11671361 | snp | A/T | 0.347848 | 0.230056 | utr-variant-3-prime, missense | NWD1 | GRCh38.p7 | 19:16815256 | CAGGAGCTCCCCAGG[A/T]CTTGGAGTCAGAAAG | 284434 |
rs11672141 | snp | A/T | 0.352287 | 0.228117 | intron-variant | NWD1 | GRCh38.p7 | 19:16730733 | aaaaaaCATTTTTTT[A/T]AAAATATATACAGGg | 284434 |
rs11672245 | snp | A/C | 0.0861826 | 0.188849 | intron-variant | NWD1 | GRCh38.p7 | 19:16761174 | tcagggctcatccac[A/C]ttgtagcagggatca | 284434 |
rs11672434 | snp | A/G | 0.386123 | 0.209692 | intron-variant | NWD1 | GRCh38.p7 | 19:16735164 | tctgtgtctcctaac[A/G]ttttacCTAACCACA | 284434 |
rs11878376 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | NWD1 | GRCh38.p7 | 19:16746449 | gaaggctgaggcaga[C/T]ggatcacgaggtcag | 284434 |
rs11879175 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | NWD1 | GRCh38.p7 | 19:16746296 | gcctaggaggcggag[A/G]ttgcagtgaaccaag | 284434 |
rs11879655 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | NWD1 | GRCh38.p7 | 19:16752270 | TTGTCGGTTACCACA[A/G]ATTCATCTAGAGGGT | 284434 |
rs11881796 | snp | C/G | 0.0592355 | 0.161582 | intron-variant | NWD1 | GRCh38.p7 | 19:16746263 | tactcaggagagtga[C/G]gtgggaggattgcgt | 284434 |
rs11882037 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NWD1 | GRCh38.p7 | 19:16802234 | ttgcattgagcacca[C/T]tgcactccagcctgg | 284434 |
rs11882301 | snp | C/T | 0.046775 | 0.145601 | intron-variant | NWD1 | GRCh38.p7 | 19:16752252 | CTGTGCCATTTCAGA[C/T]CTTTGTCGGTTACCA | 284434 |
rs11882503 | snp | C/T | 0.497776 | 0.0332724 | intron-variant | NWD1 | GRCh38.p7 | 19:16785261 | tcacgcatgtaatcc[C/T]agcagtttgggaggt | 284434 |
rs11883226 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16756014 | aatggtcgacgaaca[C/T]gtatttcatatgttc | 284434 |
rs11883276 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749046 | gagaaccaatgCACA[C/T]CCCCCAACAACAGGT | 284434 |
rs12327628 | snp | A/C | 0.147656 | 0.228091 | intron-variant | NWD1 | GRCh38.p7 | 19:16802451 | ggtgacagagcaaga[A/C]cctatctcaattaaa | 284434 |
rs12460949 | snp | C/T | 1.78717e-05 | 0.00298923 | intron-variant | NWD1 | GRCh38.p7 | 19:16762148 | CGAAAGGTGAGGTAC[C/T]TGGGACCCCCATTCC | 284434 |
rs12973121 | snp | C/T | 0.487746 | 0.0773096 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718029 | attttttgttattgt[C/T]gttgttgtagagatg | 284434 |
rs12973255 | snp | A/C | 0.48435 | 0.0870631 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718624 | ggttcatgccattct[A/C]ctgcctcagcttcct | 284434 |
rs12973836 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16791781 | tgcaatggtgtaatc[G/T]cagctcactgcaacc | 284434 |
rs12974313 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | NWD1 | GRCh38.p7 | 19:16769011 | TCTTACCCTTTGGTT[A/T]ATTTTCCATACAGCA | 284434 |
rs12974330 | snp | G/T | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16754602 | tccatccatcatctg[G/T]cttccttttatccat | 284434 |
rs12974841 | snp | A/G | 0.459687 | 0.136129 | intron-variant | NWD1 | GRCh38.p7 | 19:16776634 | ATGAGTGCATAAGAA[A/G]AAAAGTAAAAGGggc | 284434 |
rs12975018 | snp | C/G | 0.499824 | 0.00938333 | intron-variant | NWD1 | GRCh38.p7 | 19:16732568 | TAGGAGCCCCTAATG[C/G]TGTCTCCTTGTACCA | 284434 |
rs12976099 | snp | A/T | 0.454182 | 0.144256 | intron-variant | NWD1 | GRCh38.p7 | 19:16732599 | ATCCCTGGCTAGGGA[A/T]TTTTTTTTTTTTTTT | 284434 |
rs12976285 | snp | C/T | 0.420574 | 0.182769 | intron-variant | NWD1 | GRCh38.p7 | 19:16721069 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGGCCTCA | 284434 |
rs12976772 | snp | C/T | 0.332568 | 0.235971 | intron-variant | NWD1 | GRCh38.p7 | 19:16763320 | ACCTTCCATAGCTCC[C/T]CAGTGCCCTCAGTCT | 284434 |
rs12976969 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16734571 | TTTCTTTTTtttttt[C/T]ttttttctttttctg | 284434 |
rs12977898 | snp | A/C | 0.347694 | 0.230122 | intron-variant | NWD1 | GRCh38.p7 | 19:16734522 | CCTGGGTGATAGAGC[A/C]AGACTCCATCTCAAA | 284434 |
rs12980053 | snp | C/G | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16774260 | tcatacatcagttgt[C/G]cattcatccaatcat | 284434 |
rs12981111 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16725008 | caaaaatttttattt[A/T]ttttttattttttta | 284434 |
rs12982532 | snp | A/G | 0.0150014 | 0.0852976 | intron-variant | NWD1 | GRCh38.p7 | 19:16763977 | ATCTCAGAGGACCGA[A/G]CCTGGTGACTGCACC | 284434 |
rs12983375 | snp | C/T | 0.484066 | 0.0878235 | utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16720249 | TGGAATTCACTTTCT[C/T]GTGGGACAGACAAAC | 284434 |
rs12983498 | snp | A/G | 0.354881 | 0.226936 | intron-variant | NWD1 | GRCh38.p7 | 19:16731929 | GGACTATAAAAAGGC[A/G]GGTGGgactgggcgc | 284434 |
rs12984087 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732182 | agatcaagccactgt[A/C]ctccagcctgggtga | 284434 |
rs12984347 | snp | C/T | 0.336474 | 0.234568 | intron-variant | NWD1 | GRCh38.p7 | 19:16722490 | ggcggggtttctcca[C/T]gttggccaggctggt | 284434 |
rs12984426 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16734570 | CTTTCTTTTTttttt[C/T]cttttttctttttct | 284434 |
rs12984435 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16734577 | TTTttttttcttttt[C/T]ctttttctgtttttc | 284434 |
rs12984437 | snp | C/T | 0.334642 | 0.235236 | intron-variant | NWD1 | GRCh38.p7 | 19:16726588 | gggattacaggcctg[C/T]gccaccacacctggc | 284434 |
rs12984676 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16794148 | aggtgggcggatcac[C/T]tgagatcaagagttt | 284434 |
rs12984790 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NWD1 | GRCh38.p7 | 19:16766006 | tgggcaacagagtga[A/G]actccgtctcaaaaa | 284434 |
rs12986400 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718568 | cgcccaggctggagt[A/G]cagtggcgcaatctc | 284434 |
rs13343512 | snp | A/C | 0.274661 | 0.248781 | intron-variant | NWD1 | GRCh38.p7 | 19:16746693 | aaaaacaaaaaacaa[A/C]aaaaaaaaacagtcg | 284434 |
rs16981402 | snp | A/G | 0.0285073 | 0.115935 | synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749737 | GCTGCTGGGGCACAA[A/G]ACAGTGACCGTCCTG | 284434 |
rs16981403 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | NWD1 | GRCh38.p7 | 19:16753205 | CCCCTCTGGAACTTC[A/G]GCTTGCCTTGAGCCA | 284434 |
rs16981414 | snp | C/T | 0.0955749 | 0.196603 | intron-variant | NWD1 | GRCh38.p7 | 19:16771746 | GCGCTGCTGGACAAC[C/T]ATGTGCTCTCCGTAC | 284434 |
rs16995436 | snp | A/T | 0.177824 | 0.239355 | upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16719613 | GCAAGGGACTTCACC[A/T]TTCTGCATCTTGTTT | 284434 |
rs17195267 | snp | C/T | 0.338976 | 0.23363 | intron-variant | NWD1 | GRCh38.p7 | 19:16758655 | TTTCTGCATTATTTT[C/T]CTTGAGTTACCACTT | 284434 |
rs17523708 | snp | C/T | 0.361474 | 0.223771 | intron-variant | NWD1 | GRCh38.p7 | 19:16745375 | GGGAGCAATGCAGGG[C/T]GACTACCATCCCAGT | 284434 |
rs28378317 | snp | A/G | 0.106987 | 0.205054 | intron-variant | NWD1 | GRCh38.p7 | 19:16740193 | AGTCCTAGCTGCTCC[A/G]GAGGCTGAGATGGGA | 284434 |
rs28428860 | snp | C/G | 0.0681886 | 0.171594 | intron-variant | NWD1 | GRCh38.p7 | 19:16733752 | AATGCCCATGCCCGT[C/G]CTCTGACGCGGATGC | 284434 |
rs28431450 | snp | A/G | 0.407845 | 0.193868 | intron-variant | NWD1 | GRCh38.p7 | 19:16733931 | TGCTGGCCTCTCACC[A/G]CTTGTCTTAAGAATC | 284434 |
rs28461175 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16725016 | TTTATTTATTTTTTA[A/T]TTTTTTATTTTTTGA | 284434 |
rs28463833 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16792812 | AACCCGGGAGGTGGA[G/T]GTTGCAGTGAGCCGA | 284434 |
rs28473481 | snp | G/T | 0.106987 | 0.205054 | intron-variant | NWD1 | GRCh38.p7 | 19:16740026 | ATGAGGCTGGCCACC[G/T]TGGATCACACTTGTA | 284434 |
rs28504268 | snp | A/G | 0.413582 | 0.189052 | intron-variant | NWD1 | GRCh38.p7 | 19:16734033 | TCACCCCAGCCTTCC[A/G]CAGGGTCAGCTTTGC | 284434 |
rs28510720 | snp | A/C | 0.459118 | 0.137002 | intron-variant | NWD1 | GRCh38.p7 | 19:16740398 | TGGGGTGCAGTGGGA[A/C]CATGTTGGCTCACTG | 284434 |
rs28542302 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16725004 | TAGCCAAAAATTTTT[A/T]TTTATTTTTTATTTT | 284434 |
rs28570419 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787396 | AGACACTCTTAGATG[C/G]TGAATCTTTATAAAA | 284434 |
rs28650403 | snp | C/G | 0.0678174 | 0.1712 | intron-variant | NWD1 | GRCh38.p7 | 19:16733921 | CATTGAGTACTGCTG[C/G]CCTCTCACCACTTGT | 284434 |
rs28668077 | snp | C/G | 0.0681886 | 0.171594 | intron-variant | NWD1 | GRCh38.p7 | 19:16733749 | TTTAATGCCCATGCC[C/G]GTCCTCTGACGCGGA | 284434 |
rs28713378 | snp | C/T | 0.306927 | 0.243432 | intron-variant | NWD1 | GRCh38.p7 | 19:16784358 | GTAACACAGCCAGAC[C/T]CGTATCTCTAAAAAT | 284434 |
rs28759980 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782935 | CCTTTCCTTCCTTCC[C/T]TCCCTTCCTTCCCCC | 284434 |
rs28775275 | snp | C/T | | | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718289 | AAGTGATCCTCCTGC[C/T]TCAGCCTCCCAAGTA | 284434 |
rs28790729 | snp | C/T | 0.309894 | 0.242719 | intron-variant | NWD1 | GRCh38.p7 | 19:16786131 | TGGCCTTCCAAAGTG[C/T]TGGGTTTACAGGCGT | 284434 |
rs28792721 | snp | C/T | 0.309648 | 0.24278 | intron-variant | NWD1 | GRCh38.p7 | 19:16786266 | TCCCACTTCGGCCCC[C/T]GAAAGTGCTGGGATT | 284434 |
rs28794302 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782909 | TTCCATCCTTCCTTC[C/T]TTCTTTCCTTCCTTT | 284434 |
rs28800882 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782884 | TTTCTTTCTTTCTTT[C/T]TCTTTCTTTTTCCAT | 284434 |
rs28804697 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782937 | TTTCCTTCCTTCCTT[C/T]CCTTCCTTCCCCCCT | 284434 |
rs28805911 | snp | A/T | 0.323197 | 0.239044 | intron-variant | NWD1 | GRCh38.p7 | 19:16786202 | TTTTTAGAGACAGGG[A/T]CTCACTATGTTGCCC | 284434 |
rs28808942 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782920 | CTTCCTTCTTTCCTT[C/T]CTTTCCTTCCTTCCT | 284434 |
rs28820936 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782913 | ATCCTTCCTTCCTTC[C/T]TTCCTTCCTTTCCTT | 284434 |
rs28833609 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782922 | TCCTTCTTTCCTTCC[C/T]TTCCTTCCTTCCTTC | 284434 |
rs28845907 | snp | A/C | 0.31014 | 0.242659 | intron-variant | NWD1 | GRCh38.p7 | 19:16783360 | AATTTAAAGGTGGGG[A/C]ACGGTGGCTCATGCC | 284434 |
rs28887015 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782882 | TCTTTCTTTCTTTCT[C/T]TCTCTTTCTTTTTCC | 284434 |
rs34081360 | snp | C/T | 0.499846 | 0.00878459 | intron-variant | NWD1 | GRCh38.p7 | 19:16753876 | CCATCCATTCATCAA[C/T]TCGACCTTTCATCCA | 284434 |
rs34083740 | in-del | -/A | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817618 | AAAAAAAAAAAAAAA[-/A]GTAATGGCAAAAACC | 284434 |
rs34111220 | in-del | -/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16775027 | CATCTATTTATCTGC[-/G]CCACCCACAATCTCT | 284434 |
rs34165234 | in-del | -/T | 0.491834 | 0.0633738 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718170 | AGCACCTGAAACTTC[-/T]TTTTTTTTTTTTTTT | 284434 |
rs34166109 | in-del | -/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16779477 | CAGGTGAGACTTGGG[-/G]AAGTGGGCTTTGTGG | 284434 |
rs34219187 | in-del | -/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16773048 | TCTGGAGCCCCTGCA[-/G]GGGAGCAGAGACTCA | 284434 |
rs34231229 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16750627 | CCCAGCAAAATATAA[A/T]TTTTTTATTTTTATT | 284434 |
rs34274760 | in-del | -/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782951 | CCCTTCCTTCCCCCC[-/C]TTCCCCTTCCTCCCT | 284434 |
rs34349415 | snp | A/G | 0.360421 | 0.224293 | intron-variant | NWD1 | GRCh38.p7 | 19:16730254 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 284434 |
rs34509028 | in-del | -/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16779889 | GATCCTCCCTCCTTA[-/G]CCTACCAAGTAGCTG | 284434 |
rs34560566 | snp | C/T | 0.0973687 | 0.197999 | intron-variant | NWD1 | GRCh38.p7 | 19:16755663 | AAAGTGCTAGGATTA[C/T]AGGAATGAGCCACCA | 284434 |
rs34576758 | in-del | -/A | 0.492679 | 0.0600586 | intron-variant | NWD1 | GRCh38.p7 | 19:16739190 | CAAGAAAAAAAAAAA[-/A]GGAGAGAGAGGCTGA | 284434 |
rs34577966 | in-del | -/TTCT | 0.472803 | 0.113397 | intron-variant | NWD1 | GRCh38.p7 | 19:16782862 | CTTTCTTCCTTTTCC[-/TTCT]TTCTTTCTTTCTTTC | 284434 |
rs34588910 | in-del | -/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16779882 | TCAAGTGATCCTCCC[-/C]TCCTTAGCCTACCAA | 284434 |
rs34602280 | in-del | -/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16771315 | TTAGCCGGGTGTGGT[-/G]GGTGCATGCCTGTAA | 284434 |
rs34646876 | in-del | -/TAT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16742881 | TCTCACTATGTTGCC[-/TAT]TATTATTATTATTAT | 284434 |
rs34655556 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | NWD1 | GRCh38.p7 | 19:16733792 | CCTCCACACGCACAT[C/T]GGGAGACGGCGGTCC | 284434 |
rs34680514 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16723882 | GTATTTTTAGTAGAG[-/T]ACGGGGTTTCACCAT | 284434 |
rs34685366 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16721227 | GTGGGTGGGGGCCGG[-/A]AAATGCTTTGCAACA | 284434 |
rs34741739 | snp | C/T | 0.343477 | 0.231866 | intron-variant | NWD1 | GRCh38.p7 | 19:16769673 | CCCTGGGCTGGGACT[C/T]GCCTCCCCCAGCCCT | 284434 |
rs34743321 | in-del | -/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16720815 | CCTCGGCTTCCCAAA[-/G]GTGCTGGGATTACAG | 284434 |
rs34790258 | snp | C/G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16741083 | GAGAATCACTTGAAT[C/G/T]TGGGAGGCAGAGGTT | 284434 |
rs34920569 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16768438 | CTTTTGGATATTGTG[-/A]AAAGGAATCACTAGA | 284434 |
rs34938716 | in-del | -/A | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748661 | AGACCCCATCTCTAC[-/A]AAAAATACAAAAATT | 284434 |
rs35083498 | in-del | -/TTT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16731611 | AGCCCAGCCCCATGC[-/TTT]TTTTTTTTTTTTGAG | 284434 |
rs35160691 | snp | C/T | 0.396182 | 0.202807 | intron-variant | NWD1 | GRCh38.p7 | 19:16764777 | CCAGGGGACACTTGA[C/T]AATGTCTGCAGACAT | 284434 |
rs35176413 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16731921 | AATCCTTGGGACTAT[-/A]AAAAGGCAGGTGGGA | 284434 |
rs35212400 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16734768 | TTTATTTATTTATTG[G/T]AGACACAATGTCTCC | 284434 |
rs35265751 | in-del | -/A | 0.375 | 0.216506 | intron-variant | NWD1 | GRCh38.p7 | 19:16766035 | GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 284434 |
rs35267253 | snp | C/G | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749125 | CTTCCTTCCCACCTT[C/G]CCCACTTTGGCAGTC | 284434 |
rs35275095 | in-del | -/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16794241 | CATGGTGGCAGGTGC[-/C]TGTAATCCCAGCTAC | 284434 |
rs35287094 | in-del | -/C | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816124 | AATCTAGACACTTCC[-/C]ATGCACCTGGGTGAG | 284434 |
rs35290595 | in-del | -/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16812721 | CCAAGAAAAAGAGAG[-/C]ATCATATTGTCTGTT | 284434 |
rs35304287 | in-del | -/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16736997 | ATGTTGAAGCCAGAA[-/G]GGAATCTTGGAATTT | 284434 |
rs35363823 | in-del | -/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16750729 | AGTCTCCAACTCCCA[-/G]GGCTCAAGTGATCCT | 284434 |
rs35369808 | snp | A/G | 0.350982 | 0.228698 | intron-variant | NWD1 | GRCh38.p7 | 19:16731440 | GCCTCCTGAGTAGCT[A/G]GGACTACAGGTGTGC | 284434 |
rs35398561 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16788210 | ACTCCAGCCTGGGCA[-/A]CAAGAGCAAAACTTC | 284434 |
rs35414691 | in-del | -/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16807267 | GGAGGCCAAGGTGGG[-/G]TGGATCACCTGAGGT | 284434 |
rs35489695 | in-del | -/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16801506 | CTTTGGGTGGCTGAG[-/G]TGGGCGGATCACTTG | 284434 |
rs35500586 | in-del | -/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16726706 | GCCTCCCAAAGTGCT[-/G]GGGATTATAGGTGTG | 284434 |
rs35605941 | in-del | -/T | 0.421684 | 0.181726 | intron-variant | NWD1 | GRCh38.p7 | 19:16793584 | TTTGGTTTTTGGTTG[-/T]TTTTTTTTTTGAGAC | 284434 |
rs35612445 | in-del | -/A | 0.123105 | 0.215401 | intron-variant | NWD1 | GRCh38.p7 | 19:16746193 | ACCTCACCTTTATTT[-/A]AAAAAAAAAAATTAA | 284434 |
rs35642054 | in-del | -/A | 0.401037 | 0.199218 | intron-variant | NWD1 | GRCh38.p7 | 19:16734535 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAGA | 284434 |
rs35652578 | snp | C/T | 0.346368 | 0.23068 | intron-variant | NWD1 | GRCh38.p7 | 19:16751658 | ATACAAAAATTAGCC[C/T]GGCATGGTGGCGGTC | 284434 |
rs35677685 | in-del | -/C | | | frameshift-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749305 | GACACTGATGCCCAG[-/C]AACCTTCTCAGCAGC | 284434 |
rs35693034 | in-del | -/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16725505 | CCTCCTGCAGGCAAA[-/G]GATAACTAGCTAGAG | 284434 |
rs35736408 | in-del | -/A | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16798952 | TTAAAAAAAAAAAAA[-/A]CATTAAAAGTTTTGA | 284434 |
rs35797219 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16736531 | TACAGGAAGAGGCTG[G/T]CAAAAATTTTTGAAA | 284434 |
rs35799956 | in-del | -/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16743716 | AGACAGAGTCTTACT[-/C]CTGTTGCCCAGGCTG | 284434 |
rs35810105 | in-del | -/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16750782 | GTAGCTGGGACTACA[-/G]GGCATGCACCACTGT | 284434 |
rs35838598 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782306 | AAAAAAAAAAAAAAA[-/A]GTGTTTTAAATTAGC | 284434 |
rs35862513 | snp | A/C | 0.0532157 | 0.154195 | intron-variant | NWD1 | GRCh38.p7 | 19:16735557 | AATCAGTCTGGGGGC[A/C]GTGGCTCATGCCTGT | 284434 |
rs35901830 | in-del | -/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16750544 | CTGCAGTCTCCAACT[-/C]CCCAGGCTCAAGTGA | 284434 |
rs35935429 | snp | C/G | 0.495559 | 0.0469148 | intron-variant | NWD1 | GRCh38.p7 | 19:16767561 | CAGAGGTTGCAGTGA[C/G]CAGAAATCCCACCAT | 284434 |
rs35974335 | in-del | -/A | 0.359998 | 0.2245 | intron-variant | NWD1 | GRCh38.p7 | 19:16758051 | TCAAAAAAAAAAAAA[-/A]GAATTTTGGAAAGAG | 284434 |
rs35986056 | in-del | -/A/AA | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16769459 | GAGCAAAATTCCATT[-/A/AA]AAAAAAAAAAAAGAG | 284434 |
rs36024340 | in-del | -/A | 0.341685 | 0.232581 | intron-variant | NWD1 | GRCh38.p7 | 19:16733520 | ATGAGATTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 284434 |
rs36039144 | in-del | -/C | | | frameshift-variant | NWD1 | GRCh38.p7 | 19:16773290 | CAGCCCCCGGGAGGA[-/C]CCCTCCGGGCAACTC | 284434 |
rs36067398 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16756528 | ATTTATCTATCATCT[-/A]GTCTATTTATCTTTA | 284434 |
rs36081090 | snp | A/G | 0.338069 | 0.233974 | intron-variant | NWD1 | GRCh38.p7 | 19:16723943 | TCAAGTGATCGGCCC[A/G]CCTTGGCCTCCCAAA | 284434 |
rs36094175 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16762224 | CCCCTTTTTGCACTC[-/A]GAAATGTCCTCCCGA | 284434 |
rs36111644 | in-del | -/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16795541 | CTGCCTCAGTCTCCC[-/C]AAGTATCTGGGATTA | 284434 |
rs55652146 | snp | A/G | 0.100231 | 0.200173 | intron-variant | NWD1 | GRCh38.p7 | 19:16792443 | GCACTTTGGGAGGCC[A/G]GGGCAGGTGGATCAC | 284434 |
rs55663422 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16803406 | AATTTGGTGGGGGGG[G/T]GGGGACACAAATCTT | 284434 |
rs55774128 | in-del | -/TTTTTT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16809567 | TCTTTTTCTTTTTTT[-/TTTTTT]GAGATGGAGTCTTGC | 284434 |
rs55794491 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16725444 | GATCACACCACTGCA[C/T]TCCAGCCTGGGTGGC | 284434 |
rs55851814 | snp | A/G | 0.296619 | 0.245615 | intron-variant | NWD1 | GRCh38.p7 | 19:16766032 | AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 284434 |
rs55976634 | snp | A/G | 0.000899415 | 0.0211872 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744551 | CACGATACTTCCAGA[A/G]GGACGAGAATGCGTT | 284434 |
rs55989823 | snp | C/T | 0.0948562 | 0.196037 | intron-variant | NWD1 | GRCh38.p7 | 19:16761440 | GGAGTGCAGTGGCAC[C/T]ACCTCAGCTCACTGC | 284434 |
rs56162704 | snp | C/T | 0.0948562 | 0.196037 | intron-variant | NWD1 | GRCh38.p7 | 19:16761135 | GCCTTTTGTGTCTGG[C/T]TTCTTTCACTCAGCA | 284434 |
rs56175120 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16725435 | GTGAGCTATGATCAC[A/G]CCACTGCACTCCAGC | 284434 |
rs56181769 | in-del | -/AA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16810457 | AAAAAAAAAAAAAAA[-/AA]GAAAGAAAAAGAAGG | 284434 |
rs56324724 | in-del | -/T | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16767194 | TTTTTTTTTTTTTTT[-/T]GGTGAGACAGAGTCT | 284434 |
rs56683037 | in-del | -/CC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764763 | AGATTCTGCCCCCCC[-/CC]AGGGGACACTTGACA | 284434 |
rs56990164 | in-del | -/T | 0.0178098 | 0.0926698 | intron-variant | NWD1 | GRCh38.p7 | 19:16747386 | TATTTATTTATTTAA[-/T]TTTTTTTTGAGACAA | 284434 |
rs57075970 | in-del | -/AAA/AAAT/T/TAAT | 0.231775 | 0.249335 | intron-variant | NWD1 | GRCh38.p7 | 19:16790639 | GTAACATTAAAAAAA[-/AAA/AAAT/T/TAAT]AATAAATAAATAAAT | 284434 |
rs57228062 | snp | C/T | 0.203575 | 0.245652 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748006 | GTTTTGTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 284434 |
rs57256154 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16761541 | TTGTATTCTTTTTTT[-/T]TAGTACAGACAGGGT | 284434 |
rs57431091 | snp | A/G | 0.170408 | 0.236992 | intron-variant | NWD1 | GRCh38.p7 | 19:16781190 | AGATAGACGAGGGTC[A/G]GGACTAGGATGGAAA | 284434 |
rs57510672 | in-del | -/CTCTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16761347 | ACCTGTTCCCTTTCT[lengthTooLong]TTCTCTTTCTTTCTT | 284434 |
rs57643593 | in-del | -/TCCA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754052 | CCATCCATCCATCCA[-/TCCA]CCCATCATCTCGATC | 284434 |
rs57652194 | in-del | -/T | 0.317692 | 0.240661 | intron-variant | NWD1 | GRCh38.p7 | 19:16775434 | CTCTTTCAGTCTGGC[-/T]GCTCTGCCATTTTCA | 284434 |
rs57776772 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | NWD1 | GRCh38.p7 | 19:16747252 | ATGTTGCTCAGGCTG[A/G]TCTCGAACTCCTGAC | 284434 |
rs57820084 | snp | A/G | 0.132066 | 0.220435 | intron-variant | NWD1 | GRCh38.p7 | 19:16731410 | CTCCCGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 284434 |
rs57830125 | snp | C/T | 0.0941369 | 0.195465 | intron-variant | NWD1 | GRCh38.p7 | 19:16759155 | GTATCCCTCCCTCTC[C/T]TGGATTCTGCATCCT | 284434 |
rs58003040 | snp | A/G | 0.145978 | 0.227331 | intron-variant | NWD1 | GRCh38.p7 | 19:16745904 | CATGGGTGACAGAGT[A/G]AGACCCTGTCTCTAA | 284434 |
rs58025516 | in-del | -/GTTTT | 0.31357 | 0.241783 | intron-variant | NWD1 | GRCh38.p7 | 19:16766554 | AGGATGTTCTGTTTG[-/GTTTT]GTTTTAATTATAGCA | 284434 |
rs58061957 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16734570 | TTTCTTTTTTTTTTT[-/T]CTTTTTTCTTTTTCT | 284434 |
rs58224547 | snp | A/T | 0.147656 | 0.228091 | intron-variant | NWD1 | GRCh38.p7 | 19:16799675 | CCAAGCCTGGCTAAT[A/T]TTTTGTATTTTTATT | 284434 |
rs58283462 | in-del | -/AAAAA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16759027 | AAAAAAAAAAAAAAA[-/AAAAA]TCGGAAAAGGTCTTC | 284434 |
rs58317694 | snp | C/T | 0.115088 | 0.210473 | intron-variant | NWD1 | GRCh38.p7 | 19:16790743 | AAAAATAATATAAAC[C/T]ATCTCAATAATAATT | 284434 |
rs58317867 | in-del | -/TT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16778507 | TTCTTTTTTTTTTTT[-/TT]GTTGTTGTTGTTGTT | 284434 |
rs58390102 | snp | A/G | | | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16719389 | TGATCCGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 284434 |
rs58493421 | in-del | -/CTTTCTTTCCT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16761370 | CTTTCTTTCTTTCCT[-/CTTTCTTTCCT]TCTTTCTCTTTTTTT | 284434 |
rs58532395 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16781375 | TATCCCAGCACTTTA[A/G]GAGGCTGAGGCAGGC | 284434 |
rs58706713 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16741514 | GGGATTACAGGCACC[C/T]ACCACCATGCCCGGC | 284434 |
rs58756047 | in-del | -/TATTTATT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16734766 | ATTTATTTATTTATT[-/TATTTATT]GTAGACACAATGTCT | 284434 |
rs58803714 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16741557 | TATTTTTAATAGATA[C/T]GGGGTTTCGCTATGT | 284434 |
rs58821970 | in-del | -/A | 0.449473 | 0.150701 | intron-variant | NWD1 | GRCh38.p7 | 19:16725008 | CAAAAATTTTTATTT[-/A]TTTTTTATTTTTTTA | 284434 |
rs59088099 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16785869 | GACTCTTTTTTTTAA[-/A]TTTTTTTGTTTTTGA | 284434 |
rs59127289 | snp | A/G | 0.168135 | 0.236216 | intron-variant | NWD1 | GRCh38.p7 | 19:16754506 | TCCATCCATCCATCC[A/G]TCATCTCTATCTTCC | 284434 |
rs59153702 | in-del | -/AAA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16802965 | AAAAAAAAAAAAAAA[-/AAA]GACATACCTGAGACT | 284434 |
rs59213967 | snp | A/T | 0.093417 | 0.194889 | intron-variant | NWD1 | GRCh38.p7 | 19:16756145 | TTAATTCCAGCTACT[A/T]GGGAGGCTGAGTACG | 284434 |
rs59388758 | snp | A/G | 0.316968 | 0.240864 | intron-variant | NWD1 | GRCh38.p7 | 19:16770498 | ATGTCTTTATTAGCA[A/G]CATGAGAACAGACAA | 284434 |
rs59426107 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16791770 | CCAGGCTGGAGTGCA[A/G]TGGTGTAATCTCAGC | 284434 |
rs59527287 | in-del | -/TTTAT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16760276 | TTTATTTTATTTTAT[-/TTTAT]GTATTTTGAGACAGG | 284434 |
rs59759513 | snp | C/T | 0.422158 | 0.181278 | intron-variant | NWD1 | GRCh38.p7 | 19:16746145 | GGATTACTTGAGCCC[C/T]GAGTTGGAGACCAGT | 284434 |
rs59776692 | in-del | -/ATCC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754502 | TCCATCCATCCATCC[-/ATCC]ATCATCTCTATCTTC | 284434 |
rs59783116 | in-del | -/A/AA | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16775301 | AGGCTCAGATGTTGT[-/A/AA]AAAAAAAAATGGCCA | 284434 |
rs59881448 | in-del | -/AA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16728963 | AAAAAAAAAAAAAAA[-/AA]TAAGTAATTGCAGCT | 284434 |
rs59934633 | in-del | -/AAA | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16732232 | AAAAAAAAAAAAAAA[-/AAA]GGCAGATGGAGGGGT | 284434 |
rs60100694 | snp | C/T | 0.313082 | 0.241911 | intron-variant | NWD1 | GRCh38.p7 | 19:16767650 | CAGATCTCGTGAAAA[C/T]TCACTGTCATGAGAA | 284434 |
rs60100795 | in-del | -/TTTTGTTTTG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16723709 | TTTTGTTTTGTTTTG[-/TTTTGTTTTG]AGATGGACTGTCCCT | 284434 |
rs60125591 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16730293 | CGCCACTGCACTCCA[A/G]CCTGGTGACAGAGTA | 284434 |
rs60227513 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | NWD1 | GRCh38.p7 | 19:16747333 | AGCACCCGCGCCTGG[C/T]TGACATTTTCTTTTT | 284434 |
rs60291508 | in-del | -/TTTA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16755715 | TTATTTATTTATTTA[-/TTTA]GTAGAGATGGGGTCT | 284434 |
rs60410383 | in-del | -/AAGAA/AGAAA | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16737983 | AGAAAAGAAAAGAAA[-/AAGAA/AGAAA]TTCTAGAGCAGAGGC | 284434 |
rs60426474 | in-del | -/G | 0.0799831 | 0.183287 | intron-variant | NWD1 | GRCh38.p7 | 19:16755726 | TTAGTAGAGATGGGG[-/G]TCTCACTATGTTGCC | 284434 |
rs60446722 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16733521 | ATGAGATTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 284434 |
rs60536133 | snp | C/T | 0.313082 | 0.241911 | intron-variant | NWD1 | GRCh38.p7 | 19:16767543 | TTGCTTGAACACGGG[C/T]GGCAGAGGTTGCAGT | 284434 |
rs60550338 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | NWD1 | GRCh38.p7 | 19:16756251 | AGCAAGACTCTGCCT[A/C]AAAAAAATAGAAAAT | 284434 |
rs60571325 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16780714 | CCAAGCTGGAGTGCA[G/T]TGGCACAATCTCAGC | 284434 |
rs60581811 | snp | A/G | 0.0980852 | 0.198549 | intron-variant | NWD1 | GRCh38.p7 | 19:16786692 | GCTGGGATTACAGGC[A/G]CACACCACCACACCC | 284434 |
rs60597477 | in-del | -/TT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16761351 | GTTCCCTTTCTTTCT[-/TT]CTTTCTTTCTTTCTT | 284434 |
rs60646446 | in-del | -/G | 0.401747 | 0.198678 | intron-variant | NWD1 | GRCh38.p7 | 19:16733803 | ACATCGGGAGACGGC[-/G]GTCCCTCCAGAAGCA | 284434 |
rs60667961 | snp | A/G | 0.093417 | 0.194889 | intron-variant | NWD1 | GRCh38.p7 | 19:16757360 | CTCACTTCCTCCTCC[A/G]CATGGAGGGGCTGGT | 284434 |
rs60785637 | in-del | -/A | 0.0876345 | 0.190099 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816408 | AGGACTCACGCTGGC[-/A]GTAAAACAATCAACA | 284434 |
rs60849827 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16728300 | TTTTTTTTTTTTTTT[-/T]CTGAGATGGAGTCTC | 284434 |
rs60870735 | snp | C/T | 0.154993 | 0.231244 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16719287 | ATTACAGGCATGCGT[C/T]ACCACGCCCAGCTAA | 284434 |
rs61104300 | in-del | -/TTT/TTTA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16747385 | TTATTTATTTATTTA[-/TTT/TTTA]ATTTTTTTTGAGACA | 284434 |
rs61129678 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16783646 | CTCAAAAAATAAAAA[-/A]TAATAAAATAATAAA | 284434 |
rs61235274 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16741550 | ATTTTTATATTTTTA[A/G]TAGATATGGGGTTTC | 284434 |
rs61419843 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16741541 | CGGCTAATTATTTTT[A/G]TATTTTTAATAGATA | 284434 |
rs61449829 | snp | C/T | 0.49168 | 0.063958 | intron-variant | NWD1 | GRCh38.p7 | 19:16722114 | TGAGACCCTGTCTCT[C/T]GAAAAAAACAACAAC | 284434 |
rs61674251 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790645 | ATTAAAAAAAAATAA[-/A]TAAATAAATAAATAA | 284434 |
rs61675065 | in-del | -/ACTAACAAAA | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16768603 | GGGCCTGTGAATTAA[-/ACTAACAAAA]GACAGCTTAACAGGA | 284434 |
rs61731252 | snp | C/T | 0.089768 | 0.1919 | synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749791 | GAGCTCAGATGCCCG[C/T]GGCCTGCTGAAGAGC | 284434 |
rs61733271 | snp | A/G | 0.0896751 | 0.191823 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749747 | CACAAGACAGTGACC[A/G]TCCTGCGGCTGCTGG | 284434 |
rs61735363 | snp | C/T | 0.00190934 | 0.0308387 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807893 | TTACACTCAGCTGCC[C/T]GAGACCCTCTCCAGC | 284434 |
rs61735364 | snp | C/T | 0.00352545 | 0.0418365 | intron-variant | NWD1 | GRCh38.p7 | 19:16808147 | ACACGGTGGGTGGCC[C/T]GCCTCCCCATGTTCA | 284434 |
rs61736006 | snp | C/T | 0.00960081 | 0.0686165 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16759333 | GGAGCTGCTGCGCTT[C/T]CCGCCCCTGCTGTGG | 284434 |
rs61737596 | snp | A/G | 4.98467e-05 | 0.00499208 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749538 | TCTACCAAGAGATCC[A/G]CCACCACCTTTGGCA | 284434 |
rs61746179 | snp | A/G | 0.0289336 | 0.116746 | missense | NWD1 | GRCh38.p7 | 19:16750071 | GCACTGGGGGTTTTG[A/G]ACACCTTGCAGCGGG | 284434 |
rs61747578 | snp | C/T | 0.00494142 | 0.04946 | synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749372 | CTCAAGACCCACCGC[C/T]TGCCGTGGAGCCGCG | 284434 |
rs61750949 | snp | A/C/G | 0.0839546 | 0.190013 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749276 | ATGGTGGACCGGCTC[A/C/G]CGGATGGCTGCCTGG | 284434 |
rs61750950 | snp | A/G/T | 0.000924413 | 0.0214803 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749280 | TGGACCGGCTCGCGG[A/G/T]TGGCTGCCTGGACGC | 284434 |
rs61995711 | snp | C/T | 0.0327005 | 0.123616 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16761983 | CCTCTCTGTAGACAG[C/T]TGGTCGAGGTGGTCC | 284434 |
rs61998161 | snp | C/T | 0.0159636 | 0.0879031 | missense, intron-variant | NWD1 | GRCh38.p7 | 19:16749874 | TTCTGGACGCCCACA[C/T]CAGGGTGGTCCAGTT | 284434 |
rs62118202 | snp | A/G | 0.334642 | 0.235236 | intron-variant | NWD1 | GRCh38.p7 | 19:16727132 | TCAACTTACACGGGT[A/G]GGCCCCAGGGGACCC | 284434 |
rs62118244 | snp | C/G | 0.496348 | 0.0425753 | intron-variant | NWD1 | GRCh38.p7 | 19:16732722 | TCACTGCAACCTTGA[C/G]CTTCTGGGCTCAAGG | 284434 |
rs62118245 | snp | A/G | 0.489024 | 0.0732638 | intron-variant | NWD1 | GRCh38.p7 | 19:16735829 | GAAGGAAGGAAGGAA[A/G]GAAGGAAGGAAGGAA | 284434 |
rs62118246 | snp | C/T | 0.357877 | 0.225527 | intron-variant | NWD1 | GRCh38.p7 | 19:16746565 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 284434 |
rs62118247 | snp | C/T | | | missense | NWD1 | GRCh38.p7 | 19:16750297 | CCTCTTTCACCGTGC[C/T]TGTCCCGCTGGCCAC | 284434 |
rs62118249 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | NWD1 | GRCh38.p7 | 19:16759858 | AATTAGCCAGACGCG[A/G]TGGCACGTGCCTGTA | 284434 |
rs62118250 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16760262 | TTTATTTTATTTTAT[G/T]TTATTTTATTTTATG | 284434 |
rs62118251 | snp | A/G | 0.342806 | 0.232136 | intron-variant | NWD1 | GRCh38.p7 | 19:16761610 | TCAGGTGATGCACCC[A/G]CCTCAGCCTCCCAAA | 284434 |
rs62118252 | snp | A/G | 0.334182 | 0.235401 | intron-variant | NWD1 | GRCh38.p7 | 19:16761701 | GGTATATACCCAGGA[A/G]TGGATTTGCTGGGTC | 284434 |
rs62118254 | snp | C/T | 0.332568 | 0.235971 | intron-variant | NWD1 | GRCh38.p7 | 19:16765550 | TGTTGCCCAGGCTAG[C/T]CTCAAACTCCTGGGC | 284434 |
rs62118255 | snp | A/C | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16766414 | CTCAAAACGAACAAA[A/C]CAAAAAAAAACTTAT | 284434 |
rs62118259 | snp | A/T | 0.495056 | 0.049474 | intron-variant | NWD1 | GRCh38.p7 | 19:16776276 | TTTGTTCATTTTTAA[A/T]ATGAAAAGTATGGCC | 284434 |
rs62119260 | snp | A/G | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16778956 | CATGCGTTGCTGGGT[A/G]TTGAACAGCATCCCT | 284434 |
rs62119292 | snp | A/G | 0.320814 | 0.239761 | intron-variant | NWD1 | GRCh38.p7 | 19:16794049 | CAGGGGTGTACCACC[A/G]TGCCCAGCTAAAATT | 284434 |
rs62119293 | snp | C/T | 0.331179 | 0.236453 | intron-variant | NWD1 | GRCh38.p7 | 19:16796677 | CTTCTCATTTCTCTC[C/T]TTCCTCCCTTCCTCT | 284434 |
rs62119294 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | NWD1 | GRCh38.p7 | 19:16810386 | GAGGCTGCAGTGAGC[C/T]GAGAACACGCCACTA | 284434 |
rs66554819 | snp | C/T | 0.284471 | 0.247612 | intron-variant | NWD1 | GRCh38.p7 | 19:16810951 | GTTCACTGTAGCCTC[C/T]GCCTCCTGGGTTCAG | 284434 |
rs66660949 | in-del | -/GCATGCCTATAGACCTA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16752527 | CTGAGCATGGTGGTG[-/GCATGCCTATAGACCTA]CTACTCCGGAGGCTG | 284434 |
rs67106916 | in-del | -/A | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16739353 | AAAAAAAAAAAAAAA[-/A]TTATTTTTTTAAGGA | 284434 |
rs67150664 | in-del | -/AGG/G | | | intron-variant, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800440 | TGCGAGGCTGAGGCA[-/AGG/G]GAATTGTTTGAACCT | 284434 |
rs67232978 | in-del | -/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16752218 | CTCAGTTTTAGGGTT[-/G]TTTTTTTTTTTTCTC | 284434 |
rs67953014 | in-del | -/T | 0.315758 | 0.241197 | intron-variant | NWD1 | GRCh38.p7 | 19:16786182 | TTTTATTATTTTTAC[-/T]TTTTTTTTTAGAGAC | 284434 |
rs70950304 | multinucleotide-polymorphism | AG/CA | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16733191 | GAGCCACTGCACTCT[AG/CA]CCTGGGTGCCAGATT | 284434 |
rs71180317 | in-del | -/TTTTG | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16723714 | TTTTGTTTTGTTTTG[-/TTTTG]AGATGGACTGTCCCT | 284434 |
rs71180318 | in-del | -/T | 0.440609 | 0.161766 | intron-variant | NWD1 | GRCh38.p7 | 19:16725946 | GCCATAGCTACATTG[-/T]TTTTTTTTTGTTTGT | 284434 |
rs71180319 | in-del | -/T | 0.440609 | 0.161766 | intron-variant | NWD1 | GRCh38.p7 | 19:16725972 | TTTGTTTTTTTTTGC[-/T]TTTTTTTTAGACAGA | 284434 |
rs71180322 | in-del | -/TTTT | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16732614 | TTTTTTTTTTTTTTT[-/TTTT]CAGATGAGGTCCAGT | 284434 |
rs71180323 | in-del | -/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732670 | AAAAAAAAAAAAAAA[-/G]AAAAAGTGAAAAAGT | 284434 |
rs71180325 | in-del | -/A | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16737790 | AGCCTGGGCAACATA[-/A]GTGAAGTCCCATATC | 284434 |
rs71180326 | in-del | -/ATT | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16742924 | ATTATTATTATTATT[-/ATT]TTATTTGAGACAGAG | 284434 |
rs71180327 | in-del | -/A | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16751241 | AAAAAAAAAAAAAAA[-/A]TGCAATAAACTTGGG | 284434 |
rs71180328 | in-del | -/TTTATTTATTTA | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16755718 | TTATTTATTTATTTA[-/TTTATTTATTTA]GTAGAGATGGGGTCT | 284434 |
rs71180330 | in-del | -/AAAAAA | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16759026 | AAAAAAAAAAAAAAA[-/AAAAAA]TCGGAAAAGGTCTTC | 284434 |
rs71180331 | in-del | -/NTTTTT/TTTTT | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16762314 | TTTTTTTTTTTTTTT[-/NTTTTT/TTTTT]GAGACAGAGTCTTAC | 284434 |
rs71180332 | in-del | -/CATC | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16764403 | ATCCATCCATCCATC[-/CATC]TAACTATCCATTTAT | 284434 |
rs71180338 | in-del | -/A | 0.466824 | 0.124448 | intron-variant | NWD1 | GRCh38.p7 | 19:16793061 | AAAAAATTAAAAAAT[-/A]AAAAAAAAAAGAAAA | 284434 |
rs71180339 | in-del | -/GAG | 0 | 0 | intron-variant, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800441 | GCGAGGCTGAGGCAG[-/GAG]AATTGTTTGAACCTG | 284434 |
rs71334631 | in-del | -/T | 0.372794 | 0.217765 | intron-variant | NWD1 | GRCh38.p7 | 19:16734559 | AAAAGATTTTCTTTC[-/T]TTTTTTTTTTTCTTT | 284434 |
rs71334633 | in-del | -/TT/TTTT/TTTTT | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16762297 | TGTCCCCCCCACTCC[-/TT/TTTT/TTTTT]TTTTTTTTTTTTTTT | 284434 |
rs71334635 | in-del | -/G | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16785297 | GGGCACATCATTTGA[-/G]GGTCAGAAGTTCGAG | 284434 |
rs71334636 | in-del | -/A | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16790482 | GTAGGGGGTAAGGGG[-/A]AGGGAGAGCATTAGG | 284434 |
rs71336788 | snp | A/G | 0.277778 | 0.248452 | intron-variant | NWD1 | GRCh38.p7 | 19:16732670 | AAAAAAAAAAAAAAA[A/G]AAAAAGTGAAAAAGT | 284434 |
rs71336789 | snp | A/T | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16782953 | CCTTCCTTCCCCCCT[A/T]CCCCTTCCTCCCTTC | 284434 |
rs71336790 | snp | A/C | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16787910 | AATAATAATAATCAT[A/C]ATCATCATCATCATC | 284434 |
rs71336791 | snp | A/C/T | 0.161267 | 0.233723 | intron-variant | NWD1 | GRCh38.p7 | 19:16799663 | AGGCATGCACCACCA[A/C/T]GCCTGGCTAATTTTT | 284434 |
rs72099733 | in-del | -/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16789717 | CTCTCCTCTCTCTCT[-/C]TTTTTTTTTTTTTTT | 284434 |
rs72100675 | in-del | -/AAA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16802948 | TCAGACTCTGTCTCA[-/AAA]AAAAAAAAAAAAAAA | 284434 |
rs72109645 | in-del | -/AAAT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790640 | TAACATTAAAAAAAA[-/AAAT]ATAAATAAATAAATA | 284434 |
rs72483537 | in-del | -/TAT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16742900 | ATTATTATTATTATT[-/TAT]ATTATTATTATTATT | 284434 |
rs73008524 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | NWD1 | GRCh38.p7 | 19:16727689 | GTAAGGTGCAGGGTA[G/T]GGATGGGGGCTCAGA | 284434 |
rs73008544 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | NWD1 | GRCh38.p7 | 19:16735256 | TGCCTGTAATCCTAA[C/T]ATTTTGGGAGGCTGA | 284434 |
rs73008546 | snp | C/T | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16736209 | TTCCTTCCTTCCTTC[C/T]TTCCTTCCTTCCTTC | 284434 |
rs73008586 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | NWD1 | GRCh38.p7 | 19:16772103 | GAGCACAGTGGCTCA[C/T]GCCTATAATTCCAGA | 284434 |
rs73008597 | snp | C/T | 0.00282964 | 0.0375075 | missense, synonymous-codon | NWD1 | GRCh38.p7 | 19:16797828 | ACATGGTGGAGACGG[C/T]TGTTTTTGGTACTGA | 284434 |
rs73518999 | snp | G/T | 0.0376037 | 0.131863 | intron-variant | NWD1 | GRCh38.p7 | 19:16725964 | TTTTTTTGTTTGTTT[G/T]TTTTTGCTTTTTTTT | 284434 |
rs73521203 | snp | C/T | 0.0637235 | 0.166737 | intron-variant | NWD1 | GRCh38.p7 | 19:16728106 | GGAGATATTAGATAA[C/T]AGCATGCAGCTACAC | 284434 |
rs73521205 | snp | A/G | 0.114387 | 0.210022 | intron-variant | NWD1 | GRCh38.p7 | 19:16730515 | GCCTAGGAGTCTGAG[A/G]CCAGCCTAGAAAACA | 284434 |
rs73521211 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | NWD1 | GRCh38.p7 | 19:16732847 | GTGGAAACTGATGAA[C/T]ATCTTTGGAGTCTCA | 284434 |
rs73521230 | snp | A/G | 0.203882 | 0.245709 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748264 | GCTGGGATTACAGGC[A/G]TGAGACCCCATGTCC | 284434 |
rs73521233 | snp | C/T | 0.0973687 | 0.197999 | intron-variant | NWD1 | GRCh38.p7 | 19:16753553 | CCTCAGGATAGTTCT[C/T]CACGCCCCCCATCCC | 284434 |
rs73521237 | snp | C/T | 0.0952156 | 0.196321 | intron-variant | NWD1 | GRCh38.p7 | 19:16756853 | ACTCCCATTACCACC[C/T]GAGCTCCCCCTCTTG | 284434 |
rs73521241 | snp | A/G | 0.0930568 | 0.194599 | intron-variant | NWD1 | GRCh38.p7 | 19:16757447 | AGAATAAGAGTTCAG[A/G]AAAAGAGGAACTAGT | 284434 |
rs73521255 | snp | C/T | 0.0998734 | 0.199905 | intron-variant | NWD1 | GRCh38.p7 | 19:16762287 | GTCCCTTCTACTGTC[C/T]CCCCCACTCCTTTTT | 284434 |
rs73521259 | snp | C/T | 0.0998734 | 0.199905 | intron-variant | NWD1 | GRCh38.p7 | 19:16763713 | TATGTCTGTCTTCCA[C/T]TGCATTCTCGTCCAC | 284434 |
rs73521262 | snp | C/T | 0.0998734 | 0.199905 | intron-variant | NWD1 | GRCh38.p7 | 19:16764324 | TGTCAGTCTGTTCAT[C/T]CACCTATCCATCCAT | 284434 |
rs73521273 | snp | C/G | 0.0973687 | 0.197999 | intron-variant | NWD1 | GRCh38.p7 | 19:16774050 | TACACTCCCACCCTT[C/G]CATTCATCTATCCAT | 284434 |
rs73521274 | snp | C/T | 0.317692 | 0.240661 | intron-variant | NWD1 | GRCh38.p7 | 19:16775700 | TTATATGGAGTTTTG[C/T]TCTTGTCGCCCAGGC | 284434 |
rs73521275 | snp | A/G | 0.317451 | 0.240729 | intron-variant | NWD1 | GRCh38.p7 | 19:16776203 | GATCCACTGTGCCCC[A/G]CTGTACATCCTCTAG | 284434 |
rs73521279 | snp | C/T | 0.0970103 | 0.197722 | intron-variant | NWD1 | GRCh38.p7 | 19:16779777 | GAGTAGCTGGGACTA[C/T]AAGCACATACCACTA | 284434 |
rs73521283 | snp | A/G | 0.126909 | 0.217598 | intron-variant | NWD1 | GRCh38.p7 | 19:16783970 | TAATCCCAACACTTC[A/G]GGAGGCCGCGGATCA | 284434 |
rs73521285 | snp | A/G | 0.128632 | 0.218563 | intron-variant | NWD1 | GRCh38.p7 | 19:16784449 | ATACGACACTATTTC[A/G]TATAAGGCACTGGAG | 284434 |
rs73521286 | snp | C/T | 0.0980852 | 0.198549 | intron-variant | NWD1 | GRCh38.p7 | 19:16786217 | ACTCACTATGTTGCC[C/T]GGCTTGTCTCGGACT | 284434 |
rs73521295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16793250 | ATTTTGTTTTGTTTT[C/T]TGAGACAGGGTCTTA | 284434 |
rs73521299 | snp | A/G | 0.0865458 | 0.189163 | intron-variant | NWD1 | GRCh38.p7 | 19:16796605 | TGCCTGCCTCCTGCC[A/G]CTATCCCTTCCTTTC | 284434 |
rs73521300 | snp | C/T | 0.0887219 | 0.191022 | intron-variant | NWD1 | GRCh38.p7 | 19:16800500 | CCTGACTCTGCACTC[C/T]GGCCTGGGCGACAGA | 284434 |
rs73523404 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16800863 | TATCCGGCTGGCCAT[G/T]GTGGCTTAAACCTAT | 284434 |
rs73523407 | snp | A/G | 0.0872718 | 0.189788 | intron-variant | NWD1 | GRCh38.p7 | 19:16802323 | TAATGAGCTGGGCAT[A/G]GTGATATTCACCTGT | 284434 |
rs73928628 | snp | A/G | 0.00914312 | 0.0669923 | utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16720250 | GGAATTCACTTTCTC[A/G]TGGGACAGACAAACA | 284434 |
rs73928631 | snp | C/T | 0.00343046 | 0.041273 | missense, upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749159 | GAGTGGGAGATAGAG[C/T]GGAGCCTGCTGAGCT | 284434 |
rs73928646 | snp | C/G | 0.051871 | 0.152463 | intron-variant | NWD1 | GRCh38.p7 | 19:16779500 | CTTTGTGGTCAGCTT[C/G]CATAGTGAAAAGTTG | 284434 |
rs73928647 | snp | A/G | 0.0518799 | 0.152474 | intron-variant | NWD1 | GRCh38.p7 | 19:16779510 | AGCTTCCATAGTGAA[A/G]AGTTGGTTCTCAGAG | 284434 |
rs74260267 | snp | A/G | 0.182614 | 0.240747 | intron-variant | NWD1 | GRCh38.p7 | 19:16727776 | TTAAGAGACCTAGAC[A/G]TGAACCAAGTACTGT | 284434 |
rs74443045 | snp | G/T | 0.0295035 | 0.117819 | intron-variant | NWD1 | GRCh38.p7 | 19:16727681 | AGTCTCAGGTAAGGT[G/T]CAGGGTATGGATGGG | 284434 |
rs74495182 | snp | A/C | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16810438 | GTGAGACTCCATCTC[A/C]AAAAAAAAAAAAAAA | 284434 |
rs74575575 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16756825 | CTACAGCCACTTCTT[G/T]CTGCTCCTCATCACT | 284434 |
rs74579564 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NWD1 | GRCh38.p7 | 19:16770064 | TCTGTCTGCCACATC[A/G]GACTCTGAGCTCCAT | 284434 |
rs74595336 | snp | A/T | 0.499587 | 0.0143711 | intron-variant | NWD1 | GRCh38.p7 | 19:16732677 | AAAAAAAAGAAAAAG[A/T]GAAAAAGTGCAGTGG | 284434 |
rs74623654 | snp | A/C | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16766416 | CAAAACGAACAAACC[A/C]AAAAAAAACTTATTT | 284434 |
rs74671932 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NWD1 | GRCh38.p7 | 19:16737176 | ACTTCTCCCCTCTCT[C/T]TTCCAATTGCACCCC | 284434 |
rs74695110 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | NWD1 | GRCh38.p7 | 19:16775264 | TAGCTTAGTGGGAAA[G/T]AGTGTGTATTTGTTA | 284434 |
rs74706248 | snp | C/G | 0.0603597 | 0.1629 | intron-variant | NWD1 | GRCh38.p7 | 19:16778094 | CTCACTCTCTGTCCC[C/G]ATGAGGTGGAAACAA | 284434 |
rs74721035 | in-del | -/CATC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764400 | ATCCATCCATCCATC[-/CATC]TAACTATCCATTTAT | 284434 |
rs74880940 | snp | C/T | 0.444444 | 0.157135 | intron-variant | NWD1 | GRCh38.p7 | 19:16773955 | ATCCATCCATCCATC[C/T]ATCCATCCATCCATC | 284434 |
rs74887093 | snp | A/C | 0.0715223 | 0.175059 | intron-variant | NWD1 | GRCh38.p7 | 19:16736495 | AATTTGGTTCAAGTT[A/C]TTTTAATCCAGACAT | 284434 |
rs74887865 | snp | A/G | 0.000131924 | 0.00812063 | missense | NWD1 | GRCh38.p7 | 19:16762022 | TACCTGTCAGGATCC[A/G]AGAGAGCCAAGAGGC | 284434 |
rs75020273 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | NWD1 | GRCh38.p7 | 19:16762798 | CTTCCTTCCTTCCTT[C/T]CTTCCTGACAGAGTC | 284434 |
rs75092269 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816006 | AGCTCTGAGAGTGAG[A/C]CTTCTGTCCCATTCC | 284434 |
rs75216091 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16768450 | GTGAAAAGGAATCAC[C/T]AGATCACATGGAAAT | 284434 |
rs75226566 | snp | C/T | 0.00659841 | 0.0570584 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744646 | TTAACTTCTGTCCTA[C/T]GCTCTGGAGCCCAGG | 284434 |
rs75370704 | snp | G/T | 0.126564 | 0.217402 | intron-variant | NWD1 | GRCh38.p7 | 19:16727526 | CCACGCCCTTTCCAG[G/T]GGAAGGGTCATCTTG | 284434 |
rs75425433 | snp | A/C | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16735513 | TCTGTCCCCCTGACC[A/C]AAAAAAAAAAGAAAG | 284434 |
rs75466454 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | NWD1 | GRCh38.p7 | 19:16720444 | GATGCAGCATAGAGC[A/C]CTAAAGTACAGGACG | 284434 |
rs75509214 | snp | C/G | 0.0479149 | 0.147179 | intron-variant | NWD1 | GRCh38.p7 | 19:16804370 | AGGATCACTTGAGGC[C/G]AGAAGTTCGAGACCA | 284434 |
rs75624080 | snp | C/T | 0.0193772 | 0.0965046 | utr-variant-5-prime, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16719993 | GGAGTCTAAATTGGT[C/T]GTTCAACTACCAGCA | 284434 |
rs75626076 | in-del | -/TTTATTTTATTTTAT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16760262 | TTTATTTTATTTTAT[-/TTTATTTTATTTTAT]GTATTTTGAGACAGG | 284434 |
rs75649430 | snp | A/C | 0.215446 | 0.2476 | intron-variant | NWD1 | GRCh38.p7 | 19:16794644 | ACAGAGAGAAGTCCT[A/C]GGGCCAGAGGTTAGC | 284434 |
rs75813323 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16750864 | AATAAATACACACAT[G/T]TAAAAGAAAGAAAGG | 284434 |
rs75814754 | snp | G/T | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16795430 | CTTTTTTTTTTTTTT[G/T]TTTTGAGACCGAGTC | 284434 |
rs75815759 | snp | A/G | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16732234 | AAAAAAAAAAAAAAA[A/G]GGCAGATGGAGGGGT | 284434 |
rs75837617 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | NWD1 | GRCh38.p7 | 19:16793176 | TACCAAATACAACAA[C/T]GAAAGATACTCCCAA | 284434 |
rs75852123 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | NWD1 | GRCh38.p7 | 19:16730472 | TAATCCCAGTGCTTT[C/G]AGAGGCCAAAGCAAT | 284434 |
rs75873352 | snp | C/T | 0.0126979 | 0.078662 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815974 | ATTTGATTCAGGTCA[C/T]AAGTCCAAGGTGCAA | 284434 |
rs75898412 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16727784 | CCTAGACGTGAACCA[A/C]GTACTGTGTTTCACG | 284434 |
rs75900614 | snp | G/T | 0.0858192 | 0.188533 | intron-variant | NWD1 | GRCh38.p7 | 19:16752215 | CTTCTCAGTTTTAGG[G/T]TTGTTTTTTTTTTTT | 284434 |
rs75912350 | snp | A/G | 0.00152596 | 0.0275799 | splice-donor-variant | NWD1 | GRCh38.p7 | 19:16797887 | GATGCGCTCATTCAG[A/G]TGAGGGGAGATCTGG | 284434 |
rs75948938 | snp | A/G | 0.000236 | 0.0108602 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749616 | CCCGGCTTGGGCAGC[A/G]GCTCAGGCACGATGA | 284434 |
rs75960030 | snp | A/T | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16765812 | ACCTGAGGTCAGGAG[A/T]TTGAGACCAGCCTGG | 284434 |
rs75960571 | snp | C/T | 0.126909 | 0.217598 | intron-variant | NWD1 | GRCh38.p7 | 19:16738913 | ATTTCACTCCTTTTT[C/T]TTTGAGACAAGGTCT | 284434 |
rs75965205 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | NWD1 | GRCh38.p7 | 19:16768991 | TCTGCCTACTTTGGA[C/T]TCATTCTTACCCTTT | 284434 |
rs76006763 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16730180 | ACAAAAAATTAGCCA[A/G]GTGTGGTGGTGCACG | 284434 |
rs76086440 | snp | C/G | 0.0532157 | 0.154195 | intron-variant | NWD1 | GRCh38.p7 | 19:16784856 | ATCACTTGAACCCGG[C/G]GGGCGGAGGTTGCAG | 284434 |
rs76126579 | snp | G/T | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16741386 | TTTTTTTTTTTTTTT[G/T]AGACAGTCTTACTCT | 284434 |
rs76128655 | snp | C/T | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16767170 | AAAGAGGTGCGTCTT[C/T]TTTTTTTTTTTTTTT | 284434 |
rs76140937 | snp | A/C | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16802950 | CAGACTCTGTCTCAA[A/C]AAAAAAAAAAAAAAA | 284434 |
rs76144946 | snp | C/T | 0.046775 | 0.145601 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16747872 | TATTTTTGAGGTTCA[C/T]CCACATTTTAACACC | 284434 |
rs76151884 | snp | A/C | 0.021333 | 0.101051 | intron-variant | NWD1 | GRCh38.p7 | 19:16771054 | CTTCTAATCCCAGCA[A/C]TTTGGGAGGCCCAGA | 284434 |
rs76186997 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | NWD1 | GRCh38.p7 | 19:16778916 | CTGACTTCTGGGGCT[A/G]AATCTTTCTCTGGGA | 284434 |
rs76195106 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16781530 | CTGGGGCATGAGAAT[C/T]GCTTGAGCTCAGGAG | 284434 |
rs76217691 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | NWD1 | GRCh38.p7 | 19:16810774 | TCTCTCGAGCAAAAC[C/T]AACTAATAAACAAAA | 284434 |
rs76274528 | snp | G/T | 0.0103295 | 0.0711199 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817701 | TTAACTGATTTAACT[G/T]AAGAGCCCAATTAAA | 284434 |
rs76356534 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | NWD1 | GRCh38.p7 | 19:16755314 | TTGACTTCTTGGGCT[C/T]AAGCGATCCTCCCAT | 284434 |
rs76402660 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | NWD1 | GRCh38.p7 | 19:16755211 | GTCTATCATTAATAT[A/C]TCTCTCTCTCTTTTT | 284434 |
rs76406113 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | NWD1 | GRCh38.p7 | 19:16774511 | TATCCATCTACCCTA[C/T]CACTGTTTCATTTAT | 284434 |
rs76406460 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | NWD1 | GRCh38.p7 | 19:16763165 | CCCAGAGTCCCTGCA[A/G]ACTCAGCTTCATCCT | 284434 |
rs76518767 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16730174 | TAAAACACAAAAAAT[A/T]AGCCAGGTGTGGTGG | 284434 |
rs76552071 | snp | A/C | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16802947 | AGTCAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 284434 |
rs76563274 | snp | A/G | 0.00501708 | 0.0498334 | missense | NWD1 | GRCh38.p7 | 19:16750084 | TGGACACCTTGCAGC[A/G]GGTGCTCCTGGACCC | 284434 |
rs76565972 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16768604 | GGGCCTGTGAATTAA[A/G]ACAGCTTAACAGGAG | 284434 |
rs76567260 | snp | A/T | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16803775 | AAAAAAAAAAAAAAA[A/T]TTATCTGGGCGTGGT | 284434 |
rs76579211 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | NWD1 | GRCh38.p7 | 19:16765293 | TTTTCATCAATTCTC[A/G]TACCTTTCCTGTCTA | 284434 |
rs76739123 | snp | A/T | 0.0161645 | 0.0884361 | missense, upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749190 | CAGAGGACCGGGAAC[A/T]GGGAGCCACCGTCTT | 284434 |
rs76847362 | snp | A/C | 0.0479149 | 0.147179 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817953 | AAAATGCTACAACAA[A/C]TTATTGCTTATATTG | 284434 |
rs76883598 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | NWD1 | GRCh38.p7 | 19:16766172 | AAAATATAATAATAA[C/T]TGAGTACAAAACTTC | 284434 |
rs76935346 | snp | A/C | 0.0225045 | 0.103662 | intron-variant | NWD1 | GRCh38.p7 | 19:16807516 | AACAAAACAAAAAAA[A/C]CCACCAGGGAAGCAG | 284434 |
rs76961091 | snp | A/T | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16803777 | AAAAAAAAAAAAAAT[A/T]ATCTGGGCGTGGTGG | 284434 |
rs77025590 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | NWD1 | GRCh38.p7 | 19:16725326 | AAATTTTTTTTTTTT[A/T]AATTAACCAGACGTG | 284434 |
rs77031525 | snp | A/G | 0.0707826 | 0.174302 | intron-variant | NWD1 | GRCh38.p7 | 19:16774306 | TTTATCCATCAATTC[A/G]TCTATCAAACCACTT | 284434 |
rs77119467 | snp | G/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16719833 | CTAGTGCAAACAATC[G/T]CTTTCATTATCCCAG | 284434 |
rs77122896 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | NWD1 | GRCh38.p7 | 19:16774509 | TCTATCCATCTACCC[C/T]ACCACTGTTTCATTT | 284434 |
rs77129228 | snp | G/T | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16767189 | TTTTTTTTTTTTTTT[G/T]TTTTTGGTGAGACAG | 284434 |
rs77143763 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16806603 | GTAGTCCCAGTTACT[A/T]GGGGGGCTGAGGTGG | 284434 |
rs77155976 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | NWD1 | GRCh38.p7 | 19:16771021 | AGAGGGAGATGGGGC[C/T]GAGTGCGGGGGTTCA | 284434 |
rs77254566 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | NWD1 | GRCh38.p7 | 19:16768795 | GTCTCTGTATCCAAA[A/G]TGCTTCCCCATGGAT | 284434 |
rs77315388 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | NWD1 | GRCh38.p7 | 19:16722120 | CCTGTCTCTTGAAAA[A/C]AACAACAACAACAAC | 284434 |
rs77337042 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | NWD1 | GRCh38.p7 | 19:16810745 | TCCACCCTGGATGAC[G/T]ATACAAGATTCTGTC | 284434 |
rs77371695 | snp | A/C | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16735511 | ACTCTGTCCCCCTGA[A/C]CAAAAAAAAAAAGAA | 284434 |
rs77411763 | snp | G/T | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16780173 | CTTTTTTTTTTTTTT[G/T]GAGACGGAGTCTTGC | 284434 |
rs77478805 | snp | C/T | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16783043 | CTTTTCTTTCTTTCT[C/T]TTTTTTTTTTCAGGA | 284434 |
rs77488746 | snp | A/C | 0.021333 | 0.101051 | intron-variant | NWD1 | GRCh38.p7 | 19:16774769 | TTCCTTCCTTCCTCT[A/C]TTCTATCCACCCATC | 284434 |
rs77539249 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | NWD1 | GRCh38.p7 | 19:16773968 | TCCATCCATCCATCC[A/T]TCCATCCATTAATTC | 284434 |
rs77604477 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | NWD1 | GRCh38.p7 | 19:16743833 | GATTACAGGCACCTA[C/T]CACTACGCCCAGCTA | 284434 |
rs77628823 | snp | A/G/T | 0.00755907 | 0.0610114 | intron-variant | NWD1 | GRCh38.p7 | 19:16780172 | TCTTTTTTTTTTTTT[A/G/T]TGAGACGGAGTCTTG | 284434 |
rs77648787 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | NWD1 | GRCh38.p7 | 19:16733869 | TCCTTTCCTGCTCCT[C/T]TAACTCATTGTTCCT | 284434 |
rs77659325 | snp | C/G/T | 0.0611083 | 0.163768 | intron-variant | NWD1 | GRCh38.p7 | 19:16755228 | CTCTCTCTCTTTTTT[C/G/T]GGGGGGGACAGGGTC | 284434 |
rs77662171 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | NWD1 | GRCh38.p7 | 19:16778253 | AGTGTCTAGGCCCAC[A/G]TTTTCTCCAATATAT | 284434 |
rs77714951 | snp | A/T | 0.0663309 | 0.169604 | downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16818135 | AAAAAAAAAAAAAAA[A/T]TTTTTTTTAATTAGC | 284434 |
rs77751543 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | NWD1 | GRCh38.p7 | 19:16810719 | AGTGAGCTATGATCT[C/T]GCCACTGCACTCCAC | 284434 |
rs77769806 | snp | A/C | 0.00177462 | 0.0297349 | intron-variant | NWD1 | GRCh38.p7 | 19:16738178 | TCGTTCTGACAGAGA[A/C]CATCTGGCCTGTAAA | 284434 |
rs77771742 | snp | C/T | 0.350982 | 0.228698 | intron-variant | NWD1 | GRCh38.p7 | 19:16731556 | GTGATCTGCCCGCCT[C/T]GGCCTCCCAAAATGC | 284434 |
rs77784582 | snp | C/G | 0.5 | 0 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749439 | ACCTGAAGGAGCTGG[C/G]TGAGCAGTTTGTGGT | 284434 |
rs77806610 | snp | A/G | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16811586 | CGAGACTCTGTCTCA[A/G]AAAAAAAAAAAAAAG | 284434 |
rs77824997 | snp | C/T | 0.0210966 | 0.100515 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749110 | CCAATAATGACCACA[C/T]TTCCTTCCCACCTTC | 284434 |
rs77826648 | snp | C/G/T | 0.00534041 | 0.0514027 | missense, synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744429 | CTGCCAGGCCCTCAT[C/G/T]GGTGATCAGTACGGC | 284434 |
rs77837865 | snp | C/T | 0.0803491 | 0.183626 | intron-variant | NWD1 | GRCh38.p7 | 19:16752259 | ATTTCAGACCTTTGT[C/T]GGTTACCACAAATTC | 284434 |
rs77902670 | snp | G/T | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16737582 | TTTTTTTTTTTTTTT[G/T]AGATGGGTCTTGCTA | 284434 |
rs77906409 | snp | A/G | 0.0759472 | 0.179459 | intron-variant | NWD1 | GRCh38.p7 | 19:16781012 | ATTGCCAAGGATGTG[A/G]ATCAGTAAGGGTAAA | 284434 |
rs77939959 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | NWD1 | GRCh38.p7 | 19:16727441 | TGAAACTGGCTCCCC[A/G]TTCCTGATGGCCCTG | 284434 |
rs77977020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16739377 | TTTTAAGGAAGAAAG[A/G]GAAAAGAAGGGAGAC | 284434 |
rs77994493 | snp | C/T | 0.246625 | 0.249977 | intron-variant | NWD1 | GRCh38.p7 | 19:16761369 | TTCTTTCTTTCTTTC[C/T]TTCTTTCTCTTTTTT | 284434 |
rs78126258 | snp | C/G | 0.0667028 | 0.170006 | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16721480 | GGAAAACGAGAGAAG[C/G]AACAGAAATTGTGGT | 284434 |
rs78147868 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | NWD1 | GRCh38.p7 | 19:16751779 | GTGCTCCAGCCTGGG[C/T]GACAAAGGAAGACTC | 284434 |
rs78203300 | snp | A/G | 0.0193772 | 0.0965046 | utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16720144 | CCAGAAAGAGAAACA[A/G]TTGTGGAGGAAGCTG | 284434 |
rs78277164 | snp | A/T | 0.129664 | 0.219133 | intron-variant | NWD1 | GRCh38.p7 | 19:16735960 | CATAGCAGGACTCCA[A/T]CTCAAAAAAAAAAAA | 284434 |
rs78311337 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | NWD1 | GRCh38.p7 | 19:16743515 | GCCTAGCCTAGGGGA[A/C]AATTCTTTATTGACC | 284434 |
rs78421646 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NWD1 | GRCh38.p7 | 19:16727789 | ACGTGAACCAAGTAC[C/T]GTGTTTCACGCCTGT | 284434 |
rs78424294 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | NWD1 | GRCh38.p7 | 19:16770090 | TCCATAAGGCCAATG[A/G]CATCATCTGTTTTCT | 284434 |
rs78570914 | snp | C/T | 0.00172146 | 0.0292876 | missense | NWD1 | GRCh38.p7 | 19:16807648 | GAGGTTGCTGAGCAG[C/T]GCAAGCTCCTATTTA | 284434 |
rs78668156 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16756889 | TCAGCAGCATCATTA[A/G]ATTCTCATAAGAGCA | 284434 |
rs78696419 | snp | A/G | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16798727 | GACCTCCTGGGTTCA[A/G]GCAATTCTCCTGCCT | 284434 |
rs78732370 | snp | A/G | 0.0744748 | 0.178019 | intron-variant | NWD1 | GRCh38.p7 | 19:16775210 | GTTGATTTAGGGGCA[A/G]CCACTAGAATGCTGT | 284434 |
rs78748620 | snp | A/G | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16725399 | GGGAGGATCACTTGA[A/G]CCCAGGAGATCGAGG | 284434 |
rs78805740 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | NWD1 | GRCh38.p7 | 19:16774730 | TCCATTCATCCATTC[A/G]TTCATCCTTCAACCC | 284434 |
rs78846824 | snp | C/T | 0.0193772 | 0.0965046 | upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16719767 | CGTATCAGCCTGGCA[C/T]ACAATAGTTAACCAC | 284434 |
rs78870777 | snp | G/T | 0.0452528 | 0.143452 | intron-variant | NWD1 | GRCh38.p7 | 19:16737567 | TGGTCTAGTTTTAAG[G/T]TTTTTTTTTTTTTTG | 284434 |
rs78875967 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | NWD1 | GRCh38.p7 | 19:16732351 | GCTGTGTCCCTTGCA[C/G]TGTGACCTTGGACAT | 284434 |
rs78948826 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16793060 | AAAAAAATTAAAAAA[A/T]AAAAAAAAAAAGAAA | 284434 |
rs78977506 | in-del | -/TTTA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16747346 | GGCTGACATTTTCTT[-/TTTA]TTTATTTATTTATTT | 284434 |
rs79060014 | in-del | -/CCAT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16753868 | CATCCATCCATCCAT[-/CCAT]TCATCAATTCGACCT | 284434 |
rs79123183 | in-del | -/TATAATATATAATA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16738779 | TAATGATATATAATA[-/TATAATATATAATA]ACATATAACATACTA | 284434 |
rs79307399 | snp | C/T | 0.00686245 | 0.058174 | utr-variant-3-prime, missense | NWD1 | GRCh38.p7 | 19:16815163 | CAGCAAAAGCCTCAC[C/T]GCAGGACCCTCTTAA | 284434 |
rs79337417 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | NWD1 | GRCh38.p7 | 19:16732516 | GCCTTTTTCTAGAAC[A/G]CTGATGGTGTACCTG | 284434 |
rs79338519 | snp | A/G | 0.103794 | 0.20279 | intron-variant | NWD1 | GRCh38.p7 | 19:16775466 | TGTAGGGCTGTCCTC[A/G]TTGGCCCAATATAGC | 284434 |
rs79375839 | in-del | -/AT/ATAA/ATAC/ATCA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790641 | AACATTAAAAAAAAA[-/AT/ATAA/ATAC/ATCA]TAAATAAATAAATAA | 284434 |
rs79490426 | snp | A/C | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16728948 | GACTCCATCTCAAAA[A/C]AAAAAAAAAAAAAAA | 284434 |
rs79538829 | snp | C/T | 0.0944967 | 0.195752 | intron-variant | NWD1 | GRCh38.p7 | 19:16761348 | ACCTGTTCCCTTTCT[C/T]TCTCTTTCTTTCTTT | 284434 |
rs79559269 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16795397 | GCCCCAGAGGGGGTG[C/T]TACAGTGTGCTAATT | 284434 |
rs79605065 | snp | A/G | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16808627 | TCATTTTTTTTTTAA[A/G]GAGACAGGGACCCCA | 284434 |
rs79712669 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751399 | GAAAGGCAGACAGGA[A/C]GGAAGGAGACAGAAA | 284434 |
rs79793193 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16795451 | AGACCGAGTCTCGCT[C/T]TATTGCGTAGGCTGT | 284434 |
rs79902980 | snp | C/T | 0.0872718 | 0.189788 | intron-variant | NWD1 | GRCh38.p7 | 19:16808827 | GGCCAGGTGCAGTGG[C/T]TCACCCGGCACTTTG | 284434 |
rs79965240 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | NWD1 | GRCh38.p7 | 19:16804649 | ATCATATTTCTGGAG[A/G]AGGCTGGGGAGTCCA | 284434 |
rs79983092 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16727514 | GGTCTCTGAGCCCCA[C/T]GCCCTTTCCAGGGGA | 284434 |
rs80023464 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16723229 | GTTGAGATAGGGTCT[C/T]GCTCTGTTGTCCAGG | 284434 |
rs80040095 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | NWD1 | GRCh38.p7 | 19:16740680 | GAGATGGAGTTGCTC[C/T]GTTACCCAGGCTAAC | 284434 |
rs80044616 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | NWD1 | GRCh38.p7 | 19:16761312 | TGTTGTGAACATGCA[C/T]GTGTAAGGTTTTGTT | 284434 |
rs80269479 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | NWD1 | GRCh38.p7 | 19:16778915 | GCTGACTTCTGGGGC[C/T]GAATCTTTCTCTGGG | 284434 |
rs80272707 | snp | C/T | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16778496 | TCTTCTTCTTCTTCT[C/T]TTTTTTTTTTTTGTT | 284434 |
rs80327701 | in-del | -/A | 0.486846 | 0.0800249 | intron-variant | NWD1 | GRCh38.p7 | 19:16769460 | GAGCAAAATTCCATT[-/A]AAAAAAAAAAAGAGC | 284434 |
rs80332905 | snp | G/T | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16808628 | CATTTTTTTTTTAAA[G/T]AGACAGGGACCCCAC | 284434 |
rs111277754 | snp | A/T | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16736227 | CCTTCCTTCCTTCCT[A/T]CCTTCCTCTCTCTCT | 284434 |
rs111332125 | snp | A/G | 0.5 | 0 | missense | NWD1 | GRCh38.p7 | 19:16763907 | CCTATCACCTGCTTC[A/G]CTCGGGCCGCCTGGA | 284434 |
rs111348830 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16798870 | GACCTCAGGTGATCA[A/G]CTGCCTTGGCCTCCC | 284434 |
rs111356910 | in-del | -/T | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16796050 | GTGAAGGTTGGGTCA[-/T]CTCTCTCAGTGTGGC | 284434 |
rs111378531 | snp | A/T | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16790641 | TAACATTAAAAAAAA[A/T]TAAATAAATAAATAA | 284434 |
rs111395303 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817417 | AGCAGCCTGGTCAAC[A/G]TGGTGAAACTCTGTC | 284434 |
rs111397018 | snp | A/G | 0.146314 | 0.227484 | intron-variant | NWD1 | GRCh38.p7 | 19:16746614 | GGAGGCAGCGGTTGT[A/G]GTGAGCTGAGATCGC | 284434 |
rs111423166 | in-del | -/GAAG | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16729906 | AAAGAAAGAGAGAGA[-/GAAG]GAAGGAAGGAAGGAA | 284434 |
rs111428282 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | NWD1 | GRCh38.p7 | 19:16785237 | ATGTGATAGGCCAGG[C/T]GCGGTGGCTCACGCA | 284434 |
rs111484119 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | NWD1 | GRCh38.p7 | 19:16780175 | TTTTTTTTTTTTTTG[A/G]GACGGAGTCTTGCTC | 284434 |
rs111502996 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NWD1 | GRCh38.p7 | 19:16802793 | ATCATTTGAGGTCAG[A/G]TGTTCGAGACTAGCC | 284434 |
rs111519885 | in-del | -/T | 0.299916 | 0.244966 | intron-variant | NWD1 | GRCh38.p7 | 19:16786553 | TTATGTTGGGGACAC[-/T]TTTTTTTTTTTGAGA | 284434 |
rs111520121 | snp | A/G | 0.100944 | 0.200705 | intron-variant | NWD1 | GRCh38.p7 | 19:16762336 | GAGTCTTACTCTGTC[A/G]CCCAGGCTGGAGTGC | 284434 |
rs111535870 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | NWD1 | GRCh38.p7 | 19:16768149 | ACAGGTGTGTGCCAC[A/C]ACATGCAGCTAATTT | 284434 |
rs111538296 | in-del | -/AAAC | 0.154329 | 0.23097 | intron-variant | NWD1 | GRCh38.p7 | 19:16762555 | GAAACTCTGTCTCAA[-/AAAC]AAACAAACAAACAAA | 284434 |
rs111553841 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16802286 | TCAAAAATAAATAAA[A/T]AAATAAAAATAAAAA | 284434 |
rs111558341 | snp | A/G | 0.203575 | 0.245652 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748173 | ATTTTTAGTAGTGAC[A/G]AGGTTTCACCATGTT | 284434 |
rs111592008 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16808376 | CCAACATGGTGAAAC[C/T]CCGTCTCTACTAAAA | 284434 |
rs111616718 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16724921 | CTGGTCTGGAACTCC[C/T]GACCTCAGGTGGTCC | 284434 |
rs111618299 | snp | A/G | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16728176 | ACTTGATATTAACCA[A/G]GGTGGAGCATTTAAA | 284434 |
rs111618636 | in-del | -/T | 0.0126979 | 0.078662 | intron-variant | NWD1 | GRCh38.p7 | 19:16783042 | TCTTTTCTTTCTTTC[-/T]TTTTTTTTTTTCAGG | 284434 |
rs111623091 | in-del | -/A | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16733222 | TGGGATGCTGTCTTT[-/A]AAAAAAAAAAAATCT | 284434 |
rs111636698 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16786916 | TCATAACCTAATCAC[A/T]GCCTGATGAACTTTT | 284434 |
rs111664141 | snp | A/C | 0.5 | 0 | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16721536 | TGGGGAGGAGGTGCT[A/C]AGAGAGGTCTGGAGA | 284434 |
rs111676200 | snp | A/G/T | 3.29451e-05 | 0.00405851 | intron-variant, missense | NWD1 | GRCh38.p7 | 19:16812805 | GACAAGTATGTGTAC[A/G/T]TGGGCTTAAAGGATC | 284434 |
rs111687474 | in-del | -/A | 0.293294 | 0.246223 | intron-variant | NWD1 | GRCh38.p7 | 19:16807171 | CCAGAATACTGTCTC[-/A]AAAAAAAAAAAAAAA | 284434 |
rs111688584 | snp | A/C | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16781777 | TTAACAGAATCAAGT[A/C]ATCGAAAATTAGCTT | 284434 |
rs111723624 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16807434 | GGAGGTGGAGGTTAC[A/G]GTGACCTGAGATCGT | 284434 |
rs111740604 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NWD1 | GRCh38.p7 | 19:16734364 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCATCT | 284434 |
rs111744118 | snp | A/C | 0.0310518 | 0.120672 | intron-variant | NWD1 | GRCh38.p7 | 19:16770027 | CTTTAATTATGATTT[A/C]TCTTGGTTTTCTTTT | 284434 |
rs111744279 | snp | A/T | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16790640 | GTAACATTAAAAAAA[A/T]ATAAATAAATAAATA | 284434 |
rs111789529 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NWD1 | GRCh38.p7 | 19:16797595 | TCGAGTGATCTGCCC[A/G]CCTTGGCGTCCCAAA | 284434 |
rs111831936 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16776677 | TTTATGCCTATAATC[C/T]CAGCTCTTTGGGAGG | 284434 |
rs111850406 | snp | A/G | 0.0970103 | 0.197722 | intron-variant | NWD1 | GRCh38.p7 | 19:16775730 | CTGGAGTGCAGTGGC[A/G]CAATCTCGGCTCACT | 284434 |
rs111859871 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, missense | NWD1 | GRCh38.p7 | 19:16745099 | GAGGCCTCACAATCA[C/T]GGCTGAAGGCAAAGG | 284434 |
rs111880494 | snp | A/T | 0.5 | 0 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815831 | TGATGTGGACCACAG[A/T]ACCTCACAGTTTATA | 284434 |
rs111900530 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16738614 | CCAGAGAGATATTCT[A/G]TTTTCTGAGATCTAT | 284434 |
rs111952181 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NWD1 | GRCh38.p7 | 19:16734140 | AGGAGACCTTGGTAC[A/G]TCCAGTGCTGGCCAA | 284434 |
rs111956607 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | NWD1 | GRCh38.p7 | 19:16809838 | CTGGGATTACAGTCA[C/T]GAGCCACCGTGCCTG | 284434 |
rs111965214 | in-del | -/G | 0.00432119 | 0.0462809 | intron-variant | NWD1 | GRCh38.p7 | 19:16794800 | TTTTCTTTTTTTTTT[-/G]AAATAGGGTCTTGCT | 284434 |
rs112003509 | snp | A/G | 0.0948562 | 0.196037 | intron-variant | NWD1 | GRCh38.p7 | 19:16767894 | AAGTGGTATTTTACA[A/G]TATTTGTCCTTTATT | 284434 |
rs112057770 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NWD1 | GRCh38.p7 | 19:16745832 | TGAGATGAGAGGATC[A/G]CTGGAGCCCGGGAGT | 284434 |
rs112114116 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816917 | GATGTATGCTTGGAT[A/G]TATTGGGCAGCAGCT | 284434 |
rs112114398 | snp | C/T | 0.0869089 | 0.189476 | intron-variant | NWD1 | GRCh38.p7 | 19:16745508 | CCGAGGCAGGAGAAT[C/T]ACTTGAGTTCAGGAG | 284434 |
rs112170186 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | NWD1 | GRCh38.p7 | 19:16809861 | CGTGCCTGGCTGCTC[C/T]GTGCTATTTCTTTAT | 284434 |
rs112172635 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16778505 | TCTTCTTTTTTTTTT[G/T]TTTGTTGTTGTTGTT | 284434 |
rs112180762 | snp | A/G | 0.0998734 | 0.199905 | intron-variant | NWD1 | GRCh38.p7 | 19:16762442 | GCTGGGATTACAGGC[A/G]CCCGCCACCATGCCT | 284434 |
rs112183486 | snp | C/G | 0.029116 | 0.117091 | intron-variant | NWD1 | GRCh38.p7 | 19:16759976 | TCCAGCCTGGCAACA[C/G]AGCGAGACTCCATTT | 284434 |
rs112199207 | in-del | -/ACTAA | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16760172 | ACTAAACTAAACTAG[-/ACTAA]ACTAAACTAAACTAA | 284434 |
rs112223594 | in-del | -/CATC | 0.238488 | 0.270194 | intron-variant | NWD1 | GRCh38.p7 | 19:16754790 | ACCTATCATCTCTAT[-/CATC]CATCCATCCATCCAT | 284434 |
rs112247725 | snp | C/G | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16791772 | AGGCTGGAGTGCAAT[C/G]GTGTAATCTCAGCTC | 284434 |
rs112257879 | snp | C/G | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16744222 | AGTGAGACCCTATCT[C/G]TACCGAAAATAAAAA | 284434 |
rs112260115 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16752860 | AAATATTAGCTGGGC[A/G]TGGTGGCTCACACCT | 284434 |
rs112265523 | snp | A/G | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16747277 | CCTGACCTCTTGATC[A/G]GCCCGCCTTGGCCTC | 284434 |
rs112271932 | snp | A/G | 0.181022 | 0.240296 | intron-variant | NWD1 | GRCh38.p7 | 19:16776875 | TGAGCCCAAGAGTTC[A/G]AGGCTGCAGTGAGCT | 284434 |
rs112273150 | snp | A/T | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16794721 | AGACGAGACAACCTC[A/T]GTTGCAAAGACTCAA | 284434 |
rs112284735 | in-del | -/A | 0.338976 | 0.23363 | intron-variant | NWD1 | GRCh38.p7 | 19:16776942 | GTGAGACCCTATCTG[-/A]AAAAAAAAAAGAAGA | 284434 |
rs112289241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16813038 | CCATGCTCTGGAGTT[C/T]GAGAACTCCCTCCCT | 284434 |
rs112294686 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | NWD1 | GRCh38.p7 | 19:16776322 | CGCCTGTAATCCCAG[C/T]GCTTTGGGAGGTTGA | 284434 |
rs112298174 | snp | A/G | 0.00284602 | 0.0376153 | missense | NWD1 | GRCh38.p7 | 19:16789023 | GCCAAAGGGACCCTC[A/G]CCAACTCTGCTTCAA | 284434 |
rs112320677 | snp | C/T | 0.0219415 | 0.102417 | synonymous-codon, utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16799936 | CATCCTGGAAGGCGT[C/T]GGGGCCCCCGTGAGC | 284434 |
rs112320738 | in-del | -/T | 0.327445 | 0.237702 | intron-variant | NWD1 | GRCh38.p7 | 19:16804817 | GCTCCCTGGGGCCTC[-/T]TTTTTTTGTTGTTCT | 284434 |
rs112340131 | snp | G/T | 0.0930568 | 0.194599 | intron-variant | NWD1 | GRCh38.p7 | 19:16758948 | GGCGGAGGTTGCAGT[G/T]AGCCGAGATTGCACC | 284434 |
rs112393287 | snp | C/G | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16756512 | TCTGCCTATTTATAT[C/G]TATTTATCTATCATC | 284434 |
rs112423820 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16746608 | AACCCGGGAGGCAGC[A/G]GTTGTAGTGAGCTGA | 284434 |
rs112424038 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718004 | AGGCACACACCACCA[C/T]GCCCAGCTAATTTTT | 284434 |
rs112474337 | snp | C/G | 4.95143e-05 | 0.00497541 | intron-variant | NWD1 | GRCh38.p7 | 19:16759205 | GATGTGCCTCAAAGC[C/G]CCACTGGTCCTCCCT | 284434 |
rs112475128 | snp | C/T | 0.00081327 | 0.0201488 | synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749626 | GCAGCAGCTCAGGCA[C/T]GATGACAGCAAGCAG | 284434 |
rs112481140 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | NWD1 | GRCh38.p7 | 19:16786325 | ATCCTTGTTCTGTTA[C/T]TGTATTTTATTTCAT | 284434 |
rs112484749 | snp | A/G | 0.000782665 | 0.0197666 | intron-variant | NWD1 | GRCh38.p7 | 19:16794412 | AAAAATTCCAGACTT[A/G]TAACCCTTAACCCGT | 284434 |
rs112510145 | snp | A/T | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16728965 | AAAAAAAAAAAAAAA[A/T]AAGTAATTGCAGCTT | 284434 |
rs112528954 | snp | C/T | 0.0930568 | 0.194599 | intron-variant | NWD1 | GRCh38.p7 | 19:16757933 | GGTGCACACCTGTAG[C/T]CCCAGCTACATGGGA | 284434 |
rs112549465 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16784934 | GAGACTCCGTCTCCA[A/C]AAAAAAAAACAACAA | 284434 |
rs112569721 | snp | C/G | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16753557 | AGGATAGTTCTCCAC[C/G]CCCCCCATCCCCCCA | 284434 |
rs112573511 | in-del | -/A | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16776569 | AAAACTCCGTCTCAC[-/A]AAAAAAAAAAAAAAT | 284434 |
rs112578262 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16786355 | TTTATAATTTCCACC[A/G]TCAATTTCACAGGGT | 284434 |
rs112593544 | in-del | -/TTT | 0.171704 | 0.237423 | intron-variant | NWD1 | GRCh38.p7 | 19:16796696 | TCCCTTCCTCTTTAC[-/TTT]TTTTCTTCCTCTCTA | 284434 |
rs112627235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16779051 | GATGTCTCCAGAAAC[C/T]GATATGTGTCCGCTG | 284434 |
rs112670267 | in-del | -/TCCA | 0.259674 | 0.249813 | intron-variant | NWD1 | GRCh38.p7 | 19:16774326 | CAAACCACTTTCCTC[-/TCCA]TCCATCCATCCATCC | 284434 |
rs112742394 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | NWD1 | GRCh38.p7 | 19:16741104 | GGCAGAGGTTGCAGT[A/G]AGCCAAGATTGCACT | 284434 |
rs112743538 | snp | A/C | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16724069 | TTGGGGAATCCCTCA[A/C]TGGCAGAGTCTGTCC | 284434 |
rs112747257 | snp | A/C | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16764227 | CACCCTACCACAGAA[A/C]ATAATCTAGCTCCAA | 284434 |
rs112789312 | snp | C/T | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16736201 | TTCCTTCTTTCCTTC[C/T]TTCCTTCTTTCCTTC | 284434 |
rs112791293 | snp | C/T | 0.227959 | 0.249026 | intron-variant | NWD1 | GRCh38.p7 | 19:16809195 | TTCAAGCAACTCTCC[C/T]GCCTCGGCCTCCCAA | 284434 |
rs112843350 | snp | C/T | 5.0171e-05 | 0.00500829 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16773262 | TGTGCTGGTGCCCCT[C/T]GGAGGATTCCTCCAG | 284434 |
rs112844097 | snp | A/G | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16752660 | CTTATAGCTGACTCC[A/G]GGGGACATATCCCAG | 284434 |
rs112894669 | snp | C/G | 0.5 | 0 | missense, utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16799906 | GAGTCTGTCAGAACA[C/G]GGGACCCTTCTGGAC | 284434 |
rs112914774 | snp | A/G | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16812913 | AAAAGGCTCTGACCT[A/G]GGTCCTGGGCATTAG | 284434 |
rs112941036 | in-del | -/G | 0.021333 | 0.101051 | intron-variant | NWD1 | GRCh38.p7 | 19:16801928 | CAGGAGGCAGAAACA[-/G]GAAGATTGCTTGAGG | 284434 |
rs112951204 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16745909 | GTGACAGAGTGAGAC[A/C/T]CTGTCTCTAAATAAA | 284434 |
rs113004962 | snp | A/T | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16773952 | TCTATCCATCCATCC[A/T]TCCATCCATCCATCC | 284434 |
rs113024218 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16735420 | CTGAGGCAGGAGAAT[C/T]GCTTGAACTCGGGAG | 284434 |
rs113048297 | snp | A/G | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16733762 | CCCGTCCTCTGACGC[A/G]GATGCTGTCAACATC | 284434 |
rs113060599 | snp | G/T | 0.156319 | 0.231784 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748838 | CAATAATAATAATAA[G/T]AAGAAGAAGAATAAG | 284434 |
rs113063696 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NWD1 | GRCh38.p7 | 19:16802526 | GCTTCCTCTGGCCGT[A/G]TGACCTCTGCACACC | 284434 |
rs113106202 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | NWD1 | GRCh38.p7 | 19:16789861 | TAGCTGGGACTACAG[A/G]CGCACGCCACCACGC | 284434 |
rs113135145 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NWD1 | GRCh38.p7 | 19:16747100 | GGAGTGTAGTGGTGC[A/G]ATCTCAGCTCACTCC | 284434 |
rs113147867 | snp | C/T | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16739228 | CTGACCATGGTGGCT[C/T]ATGCCTGTAATCCCG | 284434 |
rs113153460 | snp | A/C | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16764772 | CCCCCCCAGGGGACA[A/C]TTGACAATGTCTGCA | 284434 |
rs113156279 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | NWD1 | GRCh38.p7 | 19:16809477 | AAACTGGATCAAATC[C/T]TGCACTGGCTTAGTG | 284434 |
rs113183734 | in-del | -/AAACTAACAA | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16768601 | AGGGGCCTGTGAATT[-/AAACTAACAA]AAGACAGCTTAACAG | 284434 |
rs113187519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16756148 | ATTCCAGCTACTTGG[A/G]AGGCTGAGTACGAGA | 284434 |
rs113192277 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NWD1 | GRCh38.p7 | 19:16783494 | ACAAAATTAGCCGGG[C/T]GTGGTGATATATACC | 284434 |
rs113195808 | snp | C/T | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16778497 | CTTCTTCTTCTTCTT[C/T]TTTTTTTTTTTGTTG | 284434 |
rs113245603 | snp | C/T | 5.43237e-05 | 0.00521142 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807587 | TTCTTCCCTGGCAGG[C/T]GAGGAACAAGATTCC | 284434 |
rs113247054 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NWD1 | GRCh38.p7 | 19:16780246 | CTGTAAGCTCTGCCT[C/T]CCAGGTTCACGCCAT | 284434 |
rs113254658 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16790462 | TAAACACTTGAAATT[C/T]GGGGGGTAGGGGGTA | 284434 |
rs113268293 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16803223 | CTCCAGCTGGCCTCG[A/G]CCTTGACCTGTGGGA | 284434 |
rs113269311 | snp | C/T | 0.165527 | 0.235296 | intron-variant | NWD1 | GRCh38.p7 | 19:16776424 | AATACAAAAATTAGC[C/T]GGGCGTTGTAGCGGA | 284434 |
rs113329073 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NWD1 | GRCh38.p7 | 19:16750961 | GCGTGGTGGCTCACA[C/T]CTGTAATTCCAGCAC | 284434 |
rs113345219 | snp | A/G | 0.0883596 | 0.190715 | intron-variant | NWD1 | GRCh38.p7 | 19:16793738 | TGTGCCACCACGCCC[A/G]GCTAATTTTTGTATT | 284434 |
rs113345639 | in-del | -/T | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16755221 | ATATCTCTCTCTCTC[-/T]TTTTTTGGGGGGGGA | 284434 |
rs113352869 | snp | A/G | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16728149 | CTCCACATTCAGTGA[A/G]GTCAGTTGGCAACTT | 284434 |
rs113371648 | snp | A/G | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16788588 | AAAAAAAAAAAGAGG[A/G]TTACATAATTGTTTT | 284434 |
rs113373075 | snp | A/G | 0.0879971 | 0.190408 | intron-variant | NWD1 | GRCh38.p7 | 19:16791813 | CCGCCTCTCGGGTTC[A/G]AGCGATTCTCACTGC | 284434 |
rs113429819 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | NWD1 | GRCh38.p7 | 19:16773923 | TCCCACCCACCCATC[C/T]ATTCATCCATCCATC | 284434 |
rs113457415 | snp | C/G | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16737107 | AGGTGGAAACCCACA[C/G]GGTCTTGGGATATTT | 284434 |
rs113460479 | snp | A/C | 0.0130921 | 0.0798413 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817835 | AGATTTCACCTACAA[A/C]TTCTGATTTTAAATG | 284434 |
rs113479099 | snp | A/G | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16808549 | CACTCCGTTTAAAAA[A/G]AAAAGAAAAGAAAAG | 284434 |
rs113483252 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NWD1 | GRCh38.p7 | 19:16767364 | TCACGCCTATAATCC[C/T]AGCACTTTGGGAGGC | 284434 |
rs113513619 | snp | C/G/T | 0.00183048 | 0.0302003 | utr-variant-3-prime, synonymous-codon | NWD1 | GRCh38.p7 | 19:16815044 | CACCCTGCTGACAGT[C/G/T]CAGTTTGTCCATGCT | 284434 |
rs113537476 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | NWD1 | GRCh38.p7 | 19:16784578 | GGGAATGAGGTTGGC[G/T]GGTCTACAGAACAGC | 284434 |
rs113546526 | snp | C/G | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16760123 | CTGTACCACTGCACT[C/G]CAGTCTGGGTGACAG | 284434 |
rs113547052 | snp | C/T | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16739517 | TGGGGCCTGACCAAC[C/T]GGCCCTGGGACCTTC | 284434 |
rs113613781 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | NWD1 | GRCh38.p7 | 19:16731666 | CTGGAGTGCAATGGT[A/G]CAATCTCAGCTCACT | 284434 |
rs113626421 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16791941 | CTGGTCTCAAACTCC[C/T]AACCTCAGATGATCT | 284434 |
rs113637010 | snp | A/T | 0.039522 | 0.134904 | intron-variant | NWD1 | GRCh38.p7 | 19:16742848 | GCTATTTTTAAAAAA[A/T]TTTTTTGTAGAGACA | 284434 |
rs113637856 | snp | C/T | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16770104 | GGCATCATCTGTTTT[C/T]TCCCTGCCAAATTTT | 284434 |
rs113639169 | snp | A/G | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16773382 | TGCCTGGGGGCAGTG[A/G]AGGCCAGGTGTTTGA | 284434 |
rs113654029 | snp | G/T | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16755715 | TTATTTATTTATTTA[G/T]TTAGTAGAGATGGGG | 284434 |
rs113659526 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16780215 | AGCTAGAGTGCAGTG[A/G]TGCAATCTCGGCTCA | 284434 |
rs113678805 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | NWD1 | GRCh38.p7 | 19:16813444 | TCATTCTTTGCCCCC[A/G]CCTTATAGATGTTAG | 284434 |
rs113725595 | in-del | -/GT | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16732676 | AAAAAAAAAGAAAAA[-/GT]GAAAAAGTGCAGTGG | 284434 |
rs113728633 | snp | G/T | 0.00613746 | 0.0550551 | stop-gained, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744622 | GCCTGTGAACCAGAG[G/T]AGGCCACCTTAACTT | 284434 |
rs113732139 | snp | A/G | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16808140 | ATGAGCTACACGGTG[A/G]GTGGCCCGCCTCCCC | 284434 |
rs113761046 | snp | C/G | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16766640 | ACCCAGGCTAGAGTA[C/G]AGTGGCATGATCTCA | 284434 |
rs113802325 | snp | C/T | 0.145978 | 0.227331 | intron-variant | NWD1 | GRCh38.p7 | 19:16746627 | GTAGTGAGCTGAGAT[C/T]GCACCACTGCACTCC | 284434 |
rs113819113 | snp | G/T | 0.0360663 | 0.129354 | intron-variant | NWD1 | GRCh38.p7 | 19:16745485 | TGTAATCCCAGAATT[G/T]TGGAAGGCCGAGGCA | 284434 |
rs113820920 | in-del | -/TAT | 0.493386 | 0.0571263 | intron-variant | NWD1 | GRCh38.p7 | 19:16755688 | CCACCACATCCAGCC[-/TAT]TTATTTATTTATTTA | 284434 |
rs113822321 | in-del | -/A | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16783641 | TCCATCTCAAAAAAT[-/A]AAAAATAATAAAATA | 284434 |
rs113837227 | snp | A/C/G/T | 0.000747631 | 0.0193205 | intron-variant | NWD1 | GRCh38.p7 | 19:16765019 | TCCCACATCCTCCCC[A/C/G/T]CTTCTCTCCCTCAGG | 284434 |
rs113837833 | snp | A/T | 0.0240643 | 0.107019 | intron-variant | NWD1 | GRCh38.p7 | 19:16785867 | TTGACTCTTTTTTTT[A/T]AATTTTTTTGTTTTT | 284434 |
rs113848257 | snp | A/G | 0.101301 | 0.200969 | intron-variant | NWD1 | GRCh38.p7 | 19:16741123 | CAAGATTGCACTATT[A/G]CACTCCAGCCTGGGT | 284434 |
rs113849685 | in-del | -/T | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16731715 | GTTCAAGCGATTCTC[-/T]CGCCTCAGCCTCCTG | 284434 |
rs113851935 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16737635 | CCTAATTTATTACAT[C/T]GAGTTCCAGATACAT | 284434 |
rs113853828 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | NWD1 | GRCh38.p7 | 19:16793008 | CAAGATTGCACCACT[A/G]CACTCCAGCCTGAGT | 284434 |
rs113858615 | snp | A/T | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16746192 | AACCTCACCTTTATT[A/T]AAAAAAAAAAAATTA | 284434 |
rs113874288 | snp | C/T | 0.10237 | 0.201756 | intron-variant | NWD1 | GRCh38.p7 | 19:16783234 | GAGACTGGGTCTCAC[C/T]GTGTTTCCCAGGCTG | 284434 |
rs113887087 | snp | A/G | 0.0898077 | 0.191933 | intron-variant | NWD1 | GRCh38.p7 | 19:16810395 | GTGAGCCGAGAACAC[A/G]CCACTACACTCCAGC | 284434 |
rs113926338 | snp | A/C | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16760077 | GGAGGATCACTTGAG[A/C]CCAGGAGTTTGAGGC | 284434 |
rs113955159 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16776691 | CCCAGCTCTTTGGGA[A/G]GCCAAGGCAAGAAGA | 284434 |
rs113955334 | snp | C/T | 0.5 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16756551 | TATCTTTATGTTTAT[C/T]TATCTCTGTATCTAT | 284434 |
rs113956515 | snp | C/G | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16780187 | TTGAGACGGAGTCTT[C/G]CTCTGTCGCCCAAGC | 284434 |
rs114007828 | snp | A/G | 0.0626037 | 0.165477 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748127 | TAGTTGGGATTACAG[A/G]CGTGCGGCATCACGC | 284434 |
rs114017892 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16722157 | TAAAAAACTAGCTAG[C/G]CATGGTGGTGTGTGC | 284434 |
rs114032231 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | NWD1 | GRCh38.p7 | 19:16757632 | TCCTCTGGGAGTGCC[A/G]AGTGAGGTGCCCGCT | 284434 |
rs114130570 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | NWD1 | GRCh38.p7 | 19:16765592 | TCTTGCCTCAGCCTC[C/T]CAGAGTGCTAGGATT | 284434 |
rs114348241 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | NWD1 | GRCh38.p7 | 19:16812360 | TCCTGGGTGTCTTTC[A/T]GTTTGGAATCAAGAT | 284434 |
rs114363592 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | NWD1 | GRCh38.p7 | 19:16797197 | AAAAAAAAAAAAATT[C/G]ATGAGTGATTACAGA | 284434 |
rs114371613 | snp | A/C | 0.0150606 | 0.0854603 | missense | NWD1 | GRCh38.p7 | 19:16789053 | AAGGATTACACGCTG[A/C]ACTTGTGGAACTTAC | 284434 |
rs114440251 | snp | C/T | 0.103082 | 0.202275 | intron-variant | NWD1 | GRCh38.p7 | 19:16783979 | CACTTCGGGAGGCCG[C/T]GGATCACCTGAGGTC | 284434 |
rs114446435 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | NWD1 | GRCh38.p7 | 19:16736082 | ACCCCATCCAGGGTA[C/T]CCCATTGCATTTCGT | 284434 |
rs114475281 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | NWD1 | GRCh38.p7 | 19:16741436 | AGTGGCACCATGTCG[A/G]TTCACTGAAACCTCC | 284434 |
rs114532922 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | NWD1 | GRCh38.p7 | 19:16777741 | TGGGAGGGAAAGGAA[A/G]GAGAGGGGAGGGAAT | 284434 |
rs114545667 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | NWD1 | GRCh38.p7 | 19:16795076 | GGCGTGAGCCATTGC[A/G]CCCAGCCCTTTCTTT | 284434 |
rs114665871 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16719476 | ATGGCTAACATCTCA[C/T]GGGCCCTTCCTGTGA | 284434 |
rs114668608 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | NWD1 | GRCh38.p7 | 19:16732743 | GGGCTCAAGGGATCC[C/T]CCTGTCTCAGCCTTC | 284434 |
rs114684735 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | NWD1 | GRCh38.p7 | 19:16787552 | CAACAGAGAGAGGCT[A/C]TCAAAACAAAACAAA | 284434 |
rs114706531 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16757590 | ATGACCATGCACAGC[C/G]CTGTTTTGCAATTCA | 284434 |
rs114791192 | snp | A/G/T | 0.0479149 | 0.147179 | intron-variant | NWD1 | GRCh38.p7 | 19:16769653 | CCAAGCTTGCGTGCC[A/G/T]GGGGCCCTGGGCTGG | 284434 |
rs114897614 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | NWD1 | GRCh38.p7 | 19:16798156 | AGAGTGGAGCAGGGT[G/T]GTGGGGGAGGAAAAT | 284434 |
rs115069890 | snp | A/G/T | 0.0614824 | 0.164198 | intron-variant | NWD1 | GRCh38.p7 | 19:16723129 | GCCTCAACCTCCTGC[A/G/T]CTCAAGTGATTCTCC | 284434 |
rs115103736 | snp | A/G | 0.000280632 | 0.0118422 | intron-variant | NWD1 | GRCh38.p7 | 19:16779468 | ACTGGACACACAGGT[A/G]AGACTTGGGAAGTGG | 284434 |
rs115108193 | snp | C/T | 0.039522 | 0.134904 | intron-variant | NWD1 | GRCh38.p7 | 19:16724751 | CAGGCTGGAGTGTAA[C/T]GGCGCCATCTTGGCT | 284434 |
rs115169744 | snp | A/G | 0.039522 | 0.134904 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748141 | GGCGTGCGGCATCAC[A/G]CTGGGCTAATTTTTG | 284434 |
rs115188313 | snp | A/G | 0.0295035 | 0.117819 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16717948 | GACTTTCTGGGCTCA[A/G]GTAATCCTCCCACCT | 284434 |
rs115264807 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | NWD1 | GRCh38.p7 | 19:16757612 | TGCAATTCAGGCTAG[A/G]CGGGTCCTCTGGGAG | 284434 |
rs115265594 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | NWD1 | GRCh38.p7 | 19:16775442 | AGTCTGGCGCTCTGC[C/T]ATTTTCAGTGTAGGG | 284434 |
rs115363537 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | NWD1 | GRCh38.p7 | 19:16787360 | TAGAAGTTGCCCCTT[A/T]TTTACGTGGTTATTA | 284434 |
rs115374796 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16753415 | ATGATGATAAGGTGG[A/T]TGATTTTGGTTGCTC | 284434 |
rs115380018 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | NWD1 | GRCh38.p7 | 19:16797187 | TCCATCTCAAAAAAA[A/C]AAAAAAATTGATGAG | 284434 |
rs115415759 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | NWD1 | GRCh38.p7 | 19:16778062 | AGAAGAAAGGAAAAG[A/G]AAACAAATCCCATCT | 284434 |
rs115420786 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | NWD1 | GRCh38.p7 | 19:16779031 | TCCCCATTGTGGCAC[C/T]TCAAGATGTCTCCAG | 284434 |
rs115451980 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | NWD1 | GRCh38.p7 | 19:16790950 | AAAATAAAATGCATA[A/G]GCCGGGTGCAGTGGC | 284434 |
rs115460904 | snp | A/C/G | 0.00993945 | 0.0698483 | intron-variant | NWD1 | GRCh38.p7 | 19:16798159 | GTGGAGCAGGGTTGT[A/C/G]GGGGAGGAAAATTCT | 284434 |
rs115471495 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | NWD1 | GRCh38.p7 | 19:16720490 | GTTGAAATAAGCTAA[A/G]TGCATTAGACTAGGG | 284434 |
rs115545495 | snp | C/T | 0.00532497 | 0.0513238 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16789118 | AGGCTCAAAAAATCC[C/T]GCTGAACCTCAGATC | 284434 |
rs115573216 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | NWD1 | GRCh38.p7 | 19:16733962 | TATGTGTCTTTCTCT[C/G]GGTGCTAAAGAATTC | 284434 |
rs115668014 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | NWD1 | GRCh38.p7 | 19:16730461 | GCTCACTCCTGTAAT[C/T]CCAGTGCTTTGAGAG | 284434 |
rs115698605 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | NWD1 | GRCh38.p7 | 19:16750564 | GGCTCAAGTGATCCT[C/G]ACGCCTCACCTGCTG | 284434 |
rs115700067 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NWD1 | GRCh38.p7 | 19:16756346 | CTTGTCATCTTCACA[C/T]TGAGTAGGCAGAGGA | 284434 |
rs115700185 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | NWD1 | GRCh38.p7 | 19:16722310 | CTTTTTTTTTTTTTG[A/G]GACGGTCTTGCTCTG | 284434 |
rs115760264 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NWD1 | GRCh38.p7 | 19:16732804 | TATCCCTGGCTAACC[A/G]GGGATGTTTCTGCCT | 284434 |
rs115764952 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | NWD1 | GRCh38.p7 | 19:16747447 | AGTGGCACGATCACG[A/G]CTCAGTGTGGCCTCC | 284434 |
rs115788362 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | NWD1 | GRCh38.p7 | 19:16776718 | AAGATCTCTTGGGCC[A/G]AGATGTTCAAGACCA | 284434 |
rs115823171 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | NWD1 | GRCh38.p7 | 19:16780678 | TCATTCTTTTTTTCT[A/G]ACAGGGTGTTGCTCT | 284434 |
rs115824654 | snp | A/C | 0.00358779 | 0.0422022 | downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16818350 | CAGCAATCATGACAA[A/C]TAATGTTTTCTCTCT | 284434 |
rs115828661 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | NWD1 | GRCh38.p7 | 19:16725536 | TTTATTTATTTATTT[A/G]ATTTTATTGTTCATT | 284434 |
rs115901417 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | NWD1 | GRCh38.p7 | 19:16727008 | CCTCGTGGGAGGGGG[C/T]GGGAAGGGCAGAATG | 284434 |
rs115959069 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16790134 | TTATAAATGGAGACA[C/T]ACAATAACTTCGTGG | 284434 |
rs115977548 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NWD1 | GRCh38.p7 | 19:16756237 | AGCCTGGGTGACAGA[A/G]CAAGACTCTGCCTCA | 284434 |
rs116006821 | snp | C/G | 0.0711525 | 0.174681 | intron-variant | NWD1 | GRCh38.p7 | 19:16759072 | ATTGCCCTAACCGTG[C/G]TTGGTACCTTGTGGG | 284434 |
rs116131382 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | NWD1 | GRCh38.p7 | 19:16769734 | CGATTCCTCAGAGAA[A/G]CCTTGTCTGGCCACC | 284434 |
rs116136661 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16764929 | AGTGTCACTACTGCT[A/G]AGCCTGAGATGCCCT | 284434 |
rs116152307 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NWD1 | GRCh38.p7 | 19:16722818 | CCTCTGGAGGGGCTG[A/G]GGATTAAGGTCAGCT | 284434 |
rs116292069 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | NWD1 | GRCh38.p7 | 19:16782333 | TAGCCAGGCATGGTG[A/G]TGTGCACCTGAAGTC | 284434 |
rs116294530 | snp | A/C/T | 0.0980852 | 0.198549 | intron-variant | NWD1 | GRCh38.p7 | 19:16788186 | AATAAGCCAGGGCCA[A/C/T]GCCACTGCACTCCAG | 284434 |
rs116344657 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | NWD1 | GRCh38.p7 | 19:16729545 | TCAAGACCAGCCTGA[A/G]CAACATGGCGAGGCC | 284434 |
rs116352943 | snp | C/T | 0.039522 | 0.134904 | intron-variant | NWD1 | GRCh38.p7 | 19:16728631 | AATTACATCCTGGTT[C/T]GGGGAATGGACACAT | 284434 |
rs116536095 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NWD1 | GRCh38.p7 | 19:16771083 | GACAGAAGGATTGCT[A/G]GAGGGCAGGAGTTCA | 284434 |
rs116603225 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NWD1 | GRCh38.p7 | 19:16795217 | CATGGCCACTGCCAC[A/G]ACTGAGCACTCAGCC | 284434 |
rs116672365 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | NWD1 | GRCh38.p7 | 19:16810040 | CTGTCTGGGCAAAAG[G/T]ATTTTTTTGTGTGTG | 284434 |
rs116685346 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | NWD1 | GRCh38.p7 | 19:16798479 | AGCCGGGCGTCATGG[C/T]ATGTGCCTGTAGTCC | 284434 |
rs116688395 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | NWD1 | GRCh38.p7 | 19:16754303 | CCATCCACCCATCAT[A/G]TCTATCTTCCATCCA | 284434 |
rs116747763 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | NWD1 | GRCh38.p7 | 19:16723521 | GTCTCCCTGTGTTGC[C/T]CAGGCTGGTCTTGAA | 284434 |
rs116872534 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | NWD1 | GRCh38.p7 | 19:16763697 | AATGGGCACATGGGG[G/T]TATGTCTGTCTTCCA | 284434 |
rs116900656 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | NWD1 | GRCh38.p7 | 19:16723634 | TGATTTTAATTTATA[A/T]CCATTCATCATAACC | 284434 |
rs116913409 | snp | A/C | 0.106278 | 0.204558 | intron-variant | NWD1 | GRCh38.p7 | 19:16734929 | CTTGCTTTTTTATTT[A/C]TTAATTTTTATTTTT | 284434 |
rs116943803 | snp | C/T | 0.00636936 | 0.0560724 | utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16724433 | GGGCGATGGAGGAGC[C/T]GGCATTCCAACCAGG | 284434 |
rs116945343 | snp | A/T | 0.0232847 | 0.105357 | intron-variant | NWD1 | GRCh38.p7 | 19:16809903 | TTATTGAAAAACCTC[A/T]GCCAGGACCCCTTTC | 284434 |
rs117111241 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NWD1 | GRCh38.p7 | 19:16782497 | CAGAAAAATGGGTGG[A/G]GGTGGAGAAGGTCTA | 284434 |
rs117203650 | snp | C/T | 0.0759472 | 0.179459 | intron-variant | NWD1 | GRCh38.p7 | 19:16786084 | TGGCCAGGCTAGTCT[C/T]GAACCCCTGACCTCA | 284434 |
rs117207794 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | NWD1 | GRCh38.p7 | 19:16796904 | TGATTACTGGCTGGG[C/T]ACGGTGGCTCAGGCC | 284434 |
rs117235935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16757297 | CAAACATCAACCATG[C/T]GAGCCCAAGAAACGC | 284434 |
rs117271259 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16724715 | TATTTTTTTTTGAGA[C/T]GAAGTTTCGCTCCTA | 284434 |
rs117325587 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | NWD1 | GRCh38.p7 | 19:16778983 | CCCTGGCCTGCACCC[A/G]CCAGATGGCAGTACT | 284434 |
rs117342820 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16753052 | TAGAGGGGTGGCCCA[C/T]TGGGCCATTCTGTTG | 284434 |
rs117353506 | snp | C/T | 0.0284184 | 0.115765 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16736665 | GGGGTATTCGGAACA[C/T]TGAAGCCACTGACCA | 284434 |
rs117451765 | snp | G/T | 0.0232847 | 0.105357 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815947 | AAACTGAGCCTTGCG[G/T]AAGTAGTTATAATTT | 284434 |
rs117464788 | snp | A/G | 0.0799831 | 0.183287 | intron-variant | NWD1 | GRCh38.p7 | 19:16758344 | TGCAGTGATGTAATC[A/G]CAGCTCACTGCAGCC | 284434 |
rs117503613 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | NWD1 | GRCh38.p7 | 19:16763694 | ACCAATGGGCACATG[A/G]GGGTATGTCTGTCTT | 284434 |
rs117575909 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | NWD1 | GRCh38.p7 | 19:16744026 | ACATGGCATAAGAAC[C/G]CTCATAAGGAAATAA | 284434 |
rs117608902 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16747910 | ACTTCATCCATTTCA[A/G]TGGCCGAATAGTATC | 284434 |
rs117690411 | snp | A/G | 0.0240405 | 0.106972 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807674 | ATTTACGGGCCTCGT[A/G]TCGGGGGTCGTCCTT | 284434 |
rs117696912 | snp | A/G | 0.00676609 | 0.0577691 | utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16724377 | ACAGACCATGCGGCC[A/G]ATGCCCTGGGAGGGA | 284434 |
rs117772843 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | NWD1 | GRCh38.p7 | 19:16783969 | GTAATCCCAACACTT[C/T]GGGAGGCCGCGGATC | 284434 |
rs117929456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16743416 | GTCTCACTATGTTGC[C/T]CAGCTAGTCTCTAAC | 284434 |
rs117941268 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | NWD1 | GRCh38.p7 | 19:16743881 | AGATATGGGATTTCA[C/T]TATGTTGGCCAGGCC | 284434 |
rs117965437 | snp | A/G | 0.000379147 | 0.0137633 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16763860 | GTGGTTCTCACATAC[A/G]GTTGCAAACCTGCGG | 284434 |
rs117998858 | snp | A/T | 0.0232847 | 0.105357 | intron-variant | NWD1 | GRCh38.p7 | 19:16811252 | ACATCCGTATAACCA[A/T]AGTAATTTAAGAAAT | 284434 |
rs118046896 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | NWD1 | GRCh38.p7 | 19:16775180 | TAAGAGACACTAAGT[A/T]CAATGCATGGAGGAG | 284434 |
rs118107491 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | NWD1 | GRCh38.p7 | 19:16802547 | TCTGCACACCCCAAC[C/T]CCCTTCACCTTTTGT | 284434 |
rs137866844 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | NWD1 | GRCh38.p7 | 19:16732716 | CACAGCTCACTGCAA[A/C]CTTGAGCTTCTGGGC | 284434 |
rs137911487 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16787355 | TTTTCTAGAAGTTGC[C/T]CCTTTTTTACGTGGT | 284434 |
rs137985867 | snp | A/G | 0.046775 | 0.145601 | intron-variant | NWD1 | GRCh38.p7 | 19:16747186 | GGATTACAGGCATGC[A/G]CCACCTCGCCTGGCT | 284434 |
rs137994009 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16725009 | AAAAATTTTTATTTA[-/T]TTTTTATTTTTTTAT | 284434 |
rs138020864 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NWD1 | GRCh38.p7 | 19:16806779 | CAGCATTTTGGGAGG[C/T]CGAGGCGGGCGGATC | 284434 |
rs138025801 | snp | A/T | 0.0364509 | 0.129988 | intron-variant | NWD1 | GRCh38.p7 | 19:16745573 | ATCTCTACAAAAAAA[A/T]AAAAAAACTTTTAAA | 284434 |
rs138057083 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16784360 | AACACAGCCAGACCC[A/G]TATCTCTAAAAATAA | 284434 |
rs138102085 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | NWD1 | GRCh38.p7 | 19:16725561 | TTCATTTATTTATTT[A/G]TTTATTTTTGAGATG | 284434 |
rs138153903 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16794970 | TATTTTTAGTACAGA[C/T]GGAGTTTCACCATGT | 284434 |
rs138160757 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16779087 | GCACTGCTAGACTAG[A/T]CAGACACTTATGACC | 284434 |
rs138176395 | in-del | -/TCTG | 0.0205511 | 0.0992634 | intron-variant | NWD1 | GRCh38.p7 | 19:16764291 | TCATGAGAGACCCTA[-/TCTG]TCTGTCTGTCTATTT | 284434 |
rs138213410 | snp | A/T | 0.00438332 | 0.0466095 | utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16720175 | TTGTGATGATAATTT[A/T]CTGAGCACCTACTAT | 284434 |
rs138221689 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | NWD1 | GRCh38.p7 | 19:16755293 | CGATCACAGCTCGCC[A/G]CAGTCTTGACTTCTT | 284434 |
rs138240084 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | NWD1 | GRCh38.p7 | 19:16804019 | AATCTGGTTGTTTCC[A/G]TTTGGCCTGTTTTAA | 284434 |
rs138255440 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16756831 | CCACTTCTTGCTGCT[A/C]CTCATCACTCCCATT | 284434 |
rs138260307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16814548 | AGGTGGAGCCTACTA[C/T]ATTGTAGTTGAATAC | 284434 |
rs138264504 | snp | A/G | 0.00565106 | 0.0528545 | missense | NWD1 | GRCh38.p7 | 19:16807909 | GAGACCCTCTCCAGC[A/G]TGGCCATTCTGACGG | 284434 |
rs138297452 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NWD1 | GRCh38.p7 | 19:16771125 | GGCAACATAGCGAGA[C/T]CCTATCTCTGTAAAA | 284434 |
rs138297508 | snp | A/G | 0.000321963 | 0.0126838 | missense | NWD1 | GRCh38.p7 | 19:16750377 | CACGGGCAGCTCCTC[A/G]TGGCCCACGTGCTGG | 284434 |
rs138326746 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16766886 | CCACTGTGCCTGACC[A/C]CCATCTTAACCATTT | 284434 |
rs138347233 | snp | C/G | 0.00539372 | 0.0516504 | missense, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800060 | GTGCCTGCACCATTT[C/G]TGGACCGCACCGGCC | 284434 |
rs138390417 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NWD1 | GRCh38.p7 | 19:16793975 | TAGCTCACTGCAGCC[C/T]CCAACTCCTAGGGGC | 284434 |
rs138418866 | snp | A/T | 0.00100077 | 0.0223469 | intron-variant | NWD1 | GRCh38.p7 | 19:16791322 | GGTCTCCTGCCAAGA[A/T]GCTGCTTCCTCTTCA | 284434 |
rs138429962 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16767501 | ATGCCTGTAGTTCCA[A/G]CTACTTGAGAGGCTG | 284434 |
rs138432345 | snp | C/T | 6.63306e-05 | 0.00575855 | missense | NWD1 | GRCh38.p7 | 19:16765144 | GAGGTTGGCCTGGTC[C/T]GTGAAGCCCTCCAGC | 284434 |
rs138478614 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16733414 | TAATCCCAGCTACTC[G/T]GGAGGCTGGGGCAGG | 284434 |
rs138501905 | snp | A/G | 0.000396661 | 0.0140774 | missense | NWD1 | GRCh38.p7 | 19:16791378 | ATCTGGAAACTGCAG[A/G]GCCGGTATTCCATAT | 284434 |
rs138566461 | in-del | -/AAT | 0.0368353 | 0.130617 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748823 | GTGAGACCCTGTCTC[-/AAT]AATAATAATAATAAT | 284434 |
rs138574216 | snp | C/T | 0.0718919 | 0.175435 | intron-variant | NWD1 | GRCh38.p7 | 19:16743109 | GTAGGGGTTTCACCA[C/T]GTTGGCCAGACTGGT | 284434 |
rs138621423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16727806 | TGTTTCACGCCTGTA[A/G]TCCCAGCACTTTGGG | 284434 |
rs138623478 | snp | C/T | 0.000814968 | 0.0201698 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807683 | CCTCGTGTCGGGGGT[C/T]GTCCTTGTGTTCCCC | 284434 |
rs138635706 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NWD1 | GRCh38.p7 | 19:16725158 | AGCTGGGACTACAGG[C/T]GTGCACCACCATGGC | 284434 |
rs138638593 | in-del | -/TGTTT | 0.419936 | 0.183362 | intron-variant | NWD1 | GRCh38.p7 | 19:16723677 | TTTTACAGCTTTTTC[-/TGTTT]TGTTTTGTTTTGTTT | 284434 |
rs138647780 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16778560 | CTCACCCAGGTTGGA[C/G]TGCAGTGGTGTGATC | 284434 |
rs138663362 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16756031 | TATTTCATATGTTCT[A/G]TGTATTACAGACTGT | 284434 |
rs138665378 | snp | A/C/T | 6.58935e-05 | 0.00573955 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807932 | TCTGACGGACTACCG[A/C/T]GTGGTCTACAGCATG | 284434 |
rs138668261 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | NWD1 | GRCh38.p7 | 19:16747282 | CCTCTTGATCGGCCC[A/G]CCTTGGCCTCCCAAA | 284434 |
rs138674028 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16774555 | TCCATCCACCCATCC[A/G]TTATTCATCGATTCA | 284434 |
rs138694867 | snp | A/T | 0.000312701 | 0.0125001 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749684 | CCAGGCATTGGAAAG[A/T]CAGCCCTGATGTGCA | 284434 |
rs138756053 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | NWD1 | GRCh38.p7 | 19:16722935 | CAAACTGTTCATGTT[C/G]TCACACATCACTGCT | 284434 |
rs138765211 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16751550 | TTACGCTTTTAATCG[C/T]AGCACTTTGGGAGGC | 284434 |
rs138771230 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NWD1 | GRCh38.p7 | 19:16810504 | TAGGCACAGCAACTC[A/G]TGCCTGTAATCCCAG | 284434 |
rs138787149 | in-del | -/CATA | 0.00874735 | 0.0655527 | intron-variant | NWD1 | GRCh38.p7 | 19:16743648 | AACAGGAAAAGAAAC[-/CATA]CATACATATTTATTT | 284434 |
rs138821864 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | NWD1 | GRCh38.p7 | 19:16792635 | TGCAGTGAGCCAAGA[C/T]TGCACCACTGCACTC | 284434 |
rs138872938 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16731171 | CCTTTCCACTAATAC[A/C]CTCCATGCCCTTCCT | 284434 |
rs138879381 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16787579 | CAAAAGTAAAAAGAG[A/G]CTGGGCACAGTGGCT | 284434 |
rs138932353 | snp | C/T | 0.00046242 | 0.0151986 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16791562 | AACACCTACCTGTGC[C/T]GTCTCAGTCCAGAAG | 284434 |
rs138934598 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NWD1 | GRCh38.p7 | 19:16762778 | TTTTCTTTTTCCCTC[C/T]CTCGCTTCCTTCCTT | 284434 |
rs138941301 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | NWD1 | GRCh38.p7 | 19:16739189 | TTTAATGAGTTTCCA[A/G]GAAAAAAAAAAAGGA | 284434 |
rs138959060 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NWD1 | GRCh38.p7 | 19:16730469 | CTGTAATCCCAGTGC[C/T]TTGAGAGGCCAAAGC | 284434 |
rs138963732 | snp | C/T | 8.30944e-05 | 0.00644518 | missense, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800121 | TCTACTTCCCCAAAA[C/T]TGGGGACAAAAACAA | 284434 |
rs138964138 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NWD1 | GRCh38.p7 | 19:16770568 | CATTGAAATCTTGGC[A/G]CTGCCACTTCTTGGC | 284434 |
rs138965567 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NWD1 | GRCh38.p7 | 19:16796570 | TTCACTGGGGACCCA[C/T]TCCTATCTGCCTAGG | 284434 |
rs138983442 | snp | A/G | 0.000412164 | 0.0143496 | missense | NWD1 | GRCh38.p7 | 19:16759271 | GTTTTGTCCCTGGAC[A/G]ACGAGGTCCTGCAGG | 284434 |
rs138995280 | snp | A/G | | | stop-gained | NWD1 | GRCh38.p7 | 19:16789096 | AGAAATTTACCATTT[A/G]GGATGGAGGCTCAAA | 284434 |
rs139038538 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | NWD1 | GRCh38.p7 | 19:16721705 | TGACCCGCACTCGCT[C/G]CCTGACTCTGCCCTT | 284434 |
rs139039123 | snp | C/G/T | 0.00517822 | 0.0506191 | intron-variant | NWD1 | GRCh38.p7 | 19:16794613 | ATCAGGTTGGAGAAG[C/G/T]GGGTGGGGCTTGGGA | 284434 |
rs139041820 | snp | C/T | 0.029116 | 0.117091 | intron-variant | NWD1 | GRCh38.p7 | 19:16800479 | AAGACTGCAGTGAGC[C/T]GGGATCCTGACTCTG | 284434 |
rs139043759 | snp | A/G | 0.000165158 | 0.0090858 | missense | NWD1 | GRCh38.p7 | 19:16797754 | AAGATCGGTGCGGAT[A/G]TTCTTGGCGGACTCG | 284434 |
rs139067191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16805020 | TTTTAAAAATATTTA[C/T]TTATTTATTTATTTT | 284434 |
rs139070797 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16742250 | CGTGGTGGCTCACGC[C/T]TGTAATCCCAGCTAC | 284434 |
rs139108504 | snp | A/G/T | 8.39742e-05 | 0.00647927 | missense | NWD1 | GRCh38.p7 | 19:16749988 | CTGTCCGCCATGCTC[A/G/T]GAGGGTTCCCTGGCT | 284434 |
rs139109286 | snp | A/G | 4.95782e-05 | 0.00497862 | missense | NWD1 | GRCh38.p7 | 19:16773173 | AGACTCCATTTCTTC[A/G]CCACCTCACATCCAG | 284434 |
rs139113141 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | NWD1 | GRCh38.p7 | 19:16727994 | TGAACCTGGGAGGCA[A/G]AGGTTGCAGTGAGCC | 284434 |
rs139116271 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | NWD1 | GRCh38.p7 | 19:16746278 | CGTGGGAGGATTGCG[C/T]CAGCCTAGGAGGCGG | 284434 |
rs139139762 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | NWD1 | GRCh38.p7 | 19:16743478 | CTCCCAAAGTGTTGG[C/G]ATTACAGGCGTGAGC | 284434 |
rs139142162 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817334 | CAAAAGCCTCGGTGG[C/T]TCACGCCTGTAATCC | 284434 |
rs139167785 | in-del | -/T | 0.0225045 | 0.103662 | intron-variant | NWD1 | GRCh38.p7 | 19:16798269 | CCTCTTGAAGTTCTC[-/T]TTTTTTCCCCCTCCT | 284434 |
rs139187881 | snp | C/T | 1.72231e-05 | 0.0029345 | intron-variant | NWD1 | GRCh38.p7 | 19:16797681 | ATGGAAGGAATGACC[C/T]TCAATCTCCTCTGGA | 284434 |
rs139225696 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16801879 | CTCTGTTAGTTCTCG[A/C/T]GAGGTTGTTAAAAAG | 284434 |
rs139244656 | snp | A/G | 0.0998734 | 0.199905 | intron-variant | NWD1 | GRCh38.p7 | 19:16785317 | AGAAGTTCGAGACCA[A/G]CCTGGACAACATGGT | 284434 |
rs139371046 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16719967 | TGTCCTCTCTAACCT[A/G]TTTCCCCAGAGGAGT | 284434 |
rs139434213 | snp | C/T | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748716 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGTGG | 284434 |
rs139466091 | in-del | -/AGGGG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16777362 | GGGAAAGAGGAGAGA[-/AGGGG]AGGGGAGGGGAAGGG | 284434 |
rs139466836 | snp | A/T | 0.0372196 | 0.131242 | intron-variant | NWD1 | GRCh38.p7 | 19:16743945 | GCCTTGGCCTCCCAA[A/T]GTGCTGGGATTACAG | 284434 |
rs139528625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16757492 | GCCCTCAACAGTTTT[A/G]CTTTTGGCAGATGAG | 284434 |
rs139536058 | snp | C/T | 0.00993419 | 0.0697739 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816217 | GCAGCCTGACTGTAG[C/T]CCAGAATCACCATGG | 284434 |
rs139539640 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16775865 | TAGAGACAGGGTTTC[A/G]CCATGTTGGCCAGGC | 284434 |
rs139552917 | snp | A/G | 0.000477598 | 0.0154457 | intron-variant, missense | NWD1 | GRCh38.p7 | 19:16812821 | TGGGCTTAAAGGATC[A/G]CTCTATACTTGTTTG | 284434 |
rs139562154 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16789490 | CCTGTAAATTTTGAC[A/G]TGTGTTTTCATTTAC | 284434 |
rs139614659 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787913 | AATAATAATCATCAT[A/C]ATCATCATCATCATC | 284434 |
rs139643617 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16795261 | AGCATGTGAGCAAGT[A/G]AATGTAGGGTCCAGC | 284434 |
rs139677330 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16733897 | CCTCCCCCTTTCTTC[C/T]TCCAGTCACATTGAG | 284434 |
rs139685734 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | NWD1 | GRCh38.p7 | 19:16812538 | GCCAGGCATGGTGGC[C/T]CATGCCTGTAATCCT | 284434 |
rs139799050 | snp | G/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16719018 | GTTTTGTTTTGTTTT[G/T]TTTGTAGAGACGGGG | 284434 |
rs139801960 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16768959 | GCTGTCTCTCCTCCA[C/G]ACAGCATCCTCGGAG | 284434 |
rs139803032 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16804894 | AAGAGGTACAATGAC[A/G]GCTCAGTGCAGCCTC | 284434 |
rs139822628 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NWD1 | GRCh38.p7 | 19:16802196 | GGGAGGCAGGAGAAT[C/T]GCTTGAGCCCGGCAG | 284434 |
rs139831363 | snp | C/G | 0.000153988 | 0.00877328 | missense, intron-variant | NWD1 | GRCh38.p7 | 19:16749835 | TGTGCCTGGCCTATG[C/G]GCTGCCCTTGCCCCC | 284434 |
rs139849705 | snp | A/C/T | 0.000431969 | 0.0146902 | missense, synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749542 | CCAAGAGATCCGCCA[A/C/T]CACCTTTGGCAGAGC | 284434 |
rs139860160 | snp | A/G | 0.000400741 | 0.0141496 | missense | NWD1 | GRCh38.p7 | 19:16762125 | TGGGGAAACCACTGA[A/G]CTTGGACCGAAAGGT | 284434 |
rs139873139 | snp | C/T | 0.00106695 | 0.0230724 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16736715 | TTGGAGGAGGTTGAC[C/T]GGTGTTGGAAAACAT | 284434 |
rs139880000 | snp | A/G | 0.000615811 | 0.0175364 | missense | NWD1 | GRCh38.p7 | 19:16779408 | ACCCAGGATGGCATC[A/G]TGGCTGTGTGGGACA | 284434 |
rs139987064 | in-del | -/TTT/TTTTT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732598 | ATCCCTGGCTAGGGA[-/TTT/TTTTT]ATTTTTTTTTTTTTT | 284434 |
rs139991241 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NWD1 | GRCh38.p7 | 19:16720903 | TTGCCCAGGCTGGAG[C/T]GCAGTGGCACGATCT | 284434 |
rs139993199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16772386 | AATAAATAGCCAGGC[A/G]CGGTGGCTCATGCCT | 284434 |
rs140011864 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16753610 | CTGGAAGCATTTTTG[G/T]TTGTCATGACTGAGC | 284434 |
rs140020603 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NWD1 | GRCh38.p7 | 19:16734147 | CTTGGTACGTCCAGT[A/G]CTGGCCAAACTAAAC | 284434 |
rs140031541 | snp | C/G | 0.031825 | 0.122064 | intron-variant | NWD1 | GRCh38.p7 | 19:16788467 | CCAGCTACATGGGAG[C/G]CTGAGGCACGAGAAT | 284434 |
rs140037890 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16780688 | TTTCTGACAGGGTGT[C/T]GCTCTGTTGCCCAAG | 284434 |
rs140045971 | snp | C/T | 0.00389947 | 0.0439833 | missense, upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749183 | CTGAGCTCAGAGGAC[C/T]GGGAACAGGGAGCCA | 284434 |
rs140055464 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | NWD1 | GRCh38.p7 | 19:16726036 | GGCACGATCTTGGCT[C/G]ACTGCAACCTCTGCC | 284434 |
rs140072242 | snp | A/G | 1.64963e-05 | 0.00287192 | utr-variant-3-prime, missense | NWD1 | GRCh38.p7 | 19:16815046 | CCCTGCTGACAGTCC[A/G]GTTTGTCCATGCTGT | 284434 |
rs140075881 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16762195 | CCCTGCCTGGCATTG[C/G]TCACCTCCTTCCTTC | 284434 |
rs140099076 | snp | A/G | 0.123452 | 0.215605 | intron-variant | NWD1 | GRCh38.p7 | 19:16811441 | ATACAAAAATTAGCC[A/G]GGCATGGTGGTGCAT | 284434 |
rs140113489 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16795792 | AGTCAGCCCCTTTCC[C/T]CATTCTGGCCTGCAG | 284434 |
rs140169812 | in-del | -/AAAT | 0.0577344 | 0.159793 | downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16818400 | TTTCTTTTGGAAGAC[-/AAAT]AATATTTTGTTATCT | 284434 |
rs140197342 | in-del | -/CCCG | | | frameshift-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749275 | ATGGTGGACCGGCTC[-/CCCG]GCGGATGGCTGCCTG | 284434 |