SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs140203703 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16756992 | ACCTGTCACTGTCTC[A/C]CATCACCCCCAGATG | 284434 |
rs140218429 | snp | A/G | 0.000381132 | 0.0137993 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749417 | AAGAACAAGACTCAC[A/G]CCTGCTACCTGAAGG | 284434 |
rs140300265 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16725738 | CTGTATTTTTAGTAG[A/C]GATGGGGTTTCACCA | 284434 |
rs140336112 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16782687 | ATCTATAGATTCAAC[C/T]GACTGTGGATTGAAA | 284434 |
rs140363806 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16810047 | GGCAAAAGGATTTTT[G/T]TGTGTGTGTGTTTTG | 284434 |
rs140411452 | snp | A/G | 5.24031e-05 | 0.00511848 | missense | NWD1 | GRCh38.p7 | 19:16762134 | CACTGAACTTGGACC[A/G]AAAGGTGAGGTACCT | 284434 |
rs140413936 | in-del | -/ATTTT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16760230 | AACATAAAATTCACC[-/ATTTT]ATTTTATTTTATTTT | 284434 |
rs140495987 | snp | C/T | 0.000115928 | 0.00761251 | missense, utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16799961 | GTGAGCCTGCTGGCC[C/T]GCGGCGGGGCTTTGG | 284434 |
rs140521597 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NWD1 | GRCh38.p7 | 19:16761685 | CTGTTTCTTAATTCT[C/T]GGTATATACCCAGGA | 284434 |
rs140557653 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | NWD1 | GRCh38.p7 | 19:16743057 | AGCTGGGATTACACC[C/T]GCACGCCACCATGCC | 284434 |
rs140602425 | snp | G/T | 1.64738e-05 | 0.00286995 | missense | NWD1 | GRCh38.p7 | 19:16789041 | AACTCTGCTTCAAAG[G/T]ATTACACGCTGCACT | 284434 |
rs140634423 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | NWD1 | GRCh38.p7 | 19:16724660 | TGCCAAGTTCCAGCC[A/T]TGAACTCAACCCAGT | 284434 |
rs140641936 | snp | C/T | 0.000839974 | 0.0204796 | missense | NWD1 | GRCh38.p7 | 19:16797825 | AAGACATGGTGGAGA[C/T]GGCTGTTTTTGGTAC | 284434 |
rs140656017 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16766616 | TTTGAGACAGGATCT[C/T]GCTTCATTACCCAGG | 284434 |
rs140685964 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | NWD1 | GRCh38.p7 | 19:16735367 | AAAAATTAGCCAGGC[A/G]TGGTGGTGCACGCCT | 284434 |
rs140702273 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16813618 | AGTAGCTGGGATTAC[A/G]GGCGCCCACCACCAC | 284434 |
rs140771991 | snp | C/G | 3.32729e-05 | 0.00407864 | stop-gained | NWD1 | GRCh38.p7 | 19:16750109 | GGACCCGGAGGCCTA[C/G]TGGGAGGTGAAGCCC | 284434 |
rs140855164 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | NWD1 | GRCh38.p7 | 19:16741037 | TGGTCGTGGGTGCCT[A/G]TAATCCCAGCTACTT | 284434 |
rs140856164 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NWD1 | GRCh38.p7 | 19:16799256 | CCTGAAGTGCAGTGG[C/T]GCAATCTCAGCTCAC | 284434 |
rs140860635 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NWD1 | GRCh38.p7 | 19:16783152 | TCCTCCCACCTCAGC[C/T]TCCTGAAGAGCTAGG | 284434 |
rs140903726 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16808650 | GGACCCCACTGTCAC[A/G]AGGCTGTAGTACAGT | 284434 |
rs140941028 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16805507 | TTAATTTTTTTAATG[A/T]TTTTGCAGAGGCAGG | 284434 |
rs140945267 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | NWD1 | GRCh38.p7 | 19:16722260 | GCCACAATAGTGCCA[C/T]TGCACTCCAGCCTGG | 284434 |
rs141011766 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NWD1 | GRCh38.p7 | 19:16730040 | TTTTAAAACTATTTA[C/T]GGGCCGGGCGCAGTG | 284434 |
rs141020615 | snp | A/G | 3.3284e-05 | 0.00407932 | utr-variant-3-prime, synonymous-codon | NWD1 | GRCh38.p7 | 19:16815266 | CCAGGACTTGGAGTC[A/G]GAAAGTGCCCAGGGA | 284434 |
rs141041717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16807137 | AGGCTGCAGTGAGCT[C/T]CAGTCTCGCCACTGC | 284434 |
rs141043101 | snp | A/G/T | 6.79025e-05 | 0.00582637 | NWD1 | 19 | allele_origin=G(germline)/T(somatic) | 19:16750304 | CACCGTGCCTGTCCC[A/G/T]CTGGCCACCACCGCA | 284434 |
rs141055598 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | NWD1 | GRCh38.p7 | 19:16770354 | TTCTTCTCTCTCCTC[C/T]CGCCTTGTGAAGAAG | 284434 |
rs141118027 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16786772 | GGCTGGTCTCGATTC[A/G]AACTCCTGAGCTCAG | 284434 |
rs141165642 | snp | A/G | 1.6486e-05 | 0.00287102 | missense | NWD1 | GRCh38.p7 | 19:16807813 | GCCTATGACAACATC[A/G]TCCTGGTGCTGGACA | 284434 |
rs141181382 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NWD1 | GRCh38.p7 | 19:16756331 | ACAAAGGTCTTCATC[C/T]TTGTCATCTTCACAT | 284434 |
rs141186357 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16780165 | CAAGGTTTCTTTTTT[G/T]TTTTTTTTGAGACGG | 284434 |
rs141232322 | snp | A/G | 0.00128807 | 0.0253451 | missense, upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749184 | TGAGCTCAGAGGACC[A/G]GGAACAGGGAGCCAC | 284434 |
rs141235836 | snp | C/G | 0.000486889 | 0.0155951 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749701 | AGCCCTGATGTGCAA[C/G]CTGGCTGAGCAGATG | 284434 |
rs141254224 | snp | G/T | 0.0170251 | 0.090679 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718365 | TTTAGTAGAGATGGG[G/T]TCTCACCATATTGGC | 284434 |
rs141265775 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | NWD1 | GRCh38.p7 | 19:16725269 | TTGGACTCCCAAAGT[G/T]CTGGGATTATAGGCA | 284434 |
rs141270028 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16786227 | TTGCCCGGCTTGTCT[C/T]GGACTCCTGGGCTCA | 284434 |
rs141273708 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16743680 | TTTATTTATTAGTTT[A/G]TTTATTTATTTATTT | 284434 |
rs141279879 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16809565 | TTTCTTTTTCTTTTT[C/T]TTTTTTTGAGATGGA | 284434 |
rs141300843 | snp | C/G/T | 0.0136528 | 0.0814873 | missense | NWD1 | GRCh38.p7 | 19:16750330 | CCGCAGAGGAAGCCA[C/G/T]GCACCAACTCTGCAC | 284434 |
rs141331666 | in-del | -/CACATTCA | 0.0217236 | 0.101931 | intron-variant | NWD1 | GRCh38.p7 | 19:16780529 | GAGTTGGCACCTGGT[-/CACATTCA]CACATTCACATTCTC | 284434 |
rs141340847 | snp | G/T | 0.0448719 | 0.142907 | intron-variant | NWD1 | GRCh38.p7 | 19:16738847 | ACATTATATATTATA[G/T]ATAATACATTATCTA | 284434 |
rs141346114 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16796174 | TTCAGGCCAGGTGCA[C/G]TGGCTCACGCCTGTA | 284434 |
rs141389385 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16790062 | GGCTTCTGAAAACAA[G/T]GTCTGTTCCACTGTG | 284434 |
rs141409055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16736420 | GGGCATCTTGAAGAA[C/T]GCCCTTCCCTCTAGT | 284434 |
rs141414428 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NWD1 | GRCh38.p7 | 19:16794714 | GCAGTCCAGACGAGA[C/T]AACCTCAGTTGCAAA | 284434 |
rs141437037 | snp | C/T | 4.97302e-05 | 0.00498624 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749369 | GTCCTCAAGACCCAC[C/T]GCCTGCCGTGGAGCC | 284434 |
rs141442968 | snp | G/T | 0.000153988 | 0.00877328 | missense, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800045 | GCTCATAGGTCCCGG[G/T]TGCCTGCACCATTTC | 284434 |
rs141485925 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16732078 | AAAAATTAGCCGGGC[A/G]TGGTGGCTCATGCCT | 284434 |
rs141501682 | in-del | -/CCAT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16774145 | CATCCATCTACTGCC[-/CCAT]CCATCCATCCATCCA | 284434 |
rs141519940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16791147 | GCTGAGGCAGGAGGA[C/T]TGCTTGAGCCCAGGA | 284434 |
rs141531770 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16770702 | GCTGGGAAGAGTACG[C/T]GCATCAGTTCACACA | 284434 |
rs141533810 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16806088 | ATGTTGGCCAGACTG[A/G]TCTCAAACTCCTGAC | 284434 |
rs141569227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16804903 | AATGACGGCTCAGTG[C/T]AGCCTCGAACTCCTG | 284434 |
rs141578762 | snp | C/G | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815402 | TTAATCTAGTTAAAG[C/G]AAAAAGAATACGTTT | 284434 |
rs141584843 | snp | C/T | 0.000153988 | 0.00877328 | missense | NWD1 | GRCh38.p7 | 19:16773177 | TCCATTTCTTCGCCA[C/T]CTCACATCCAGCACT | 284434 |
rs141647701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16775782 | AAGCCATTTTCCTGC[C/T]TCAGCCTCCCAAGTA | 284434 |
rs141659198 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NWD1 | GRCh38.p7 | 19:16730799 | TTTGGGAGGCTGAGG[C/T]GGGAAGATGGCTTGA | 284434 |
rs141666135 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | NWD1 | GRCh38.p7 | 19:16808232 | ACCATGGGCCATCGA[C/T]CAGGATGGGACTGGG | 284434 |
rs141750567 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16772071 | CTGATCCTACTTTTA[C/T]TGAAAAGGTTGAGTC | 284434 |
rs141762214 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | NWD1 | GRCh38.p7 | 19:16723913 | GTTGGCCGCGCTGGT[C/G]TCCGACTCCTAACCT | 284434 |
rs141775503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16778945 | GATGGGGTTGTCATG[C/T]GTTGCTGGGTGTTGA | 284434 |
rs141798756 | snp | C/G | 0.0197955 | 0.097702 | intron-variant | NWD1 | GRCh38.p7 | 19:16723423 | AGGCTGGTCTTGAAC[C/G]CTTGGACTCCCAAAG | 284434 |
rs141813029 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | NWD1 | GRCh38.p7 | 19:16775035 | TTATCTGCCCACCCA[A/C]AATCTCTCACACTGA | 284434 |
rs141835953 | snp | G/T | 0.00490113 | 0.0492599 | missense | NWD1 | GRCh38.p7 | 19:16763861 | TGGTTCTCACATACG[G/T]TTGCAAACCTGCGGA | 284434 |
rs141852361 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NWD1 | GRCh38.p7 | 19:16807512 | ACAAAACAAAACAAA[A/G]AAAACCACCAGGGAA | 284434 |
rs141855753 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16797581 | TCGAACTCCTGACCT[C/T]GAGTGATCTGCCCGC | 284434 |
rs141907855 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | NWD1 | GRCh38.p7 | 19:16722251 | CTGCAGTGAGCCACA[A/G]TAGTGCCACTGCACT | 284434 |
rs141939535 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | NWD1 | GRCh38.p7 | 19:16759759 | TAGCACTTTGGGAGG[C/T]TGAGGTGGCGGATCA | 284434 |
rs141950749 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16792539 | TACAAAAAATTAGCC[A/G]GGCGTGGTGGTGAGC | 284434 |
rs142060061 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | NWD1 | GRCh38.p7 | 19:16737954 | TGGGCGACAGAGCAA[A/G]ACTCTATCTCGAAAA | 284434 |
rs142062634 | in-del | -/T | 0.0193772 | 0.0965046 | intron-variant | NWD1 | GRCh38.p7 | 19:16720319 | TGCAGAAAATTAAAA[-/T]AAGGCGATGGCATTG | 284434 |
rs142114542 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | NWD1 | GRCh38.p7 | 19:16742707 | CGGAGTTTCGCTCTT[A/G]TTGCCCAGGCTGGAG | 284434 |
rs142164743 | snp | C/T | 0.00159872 | 0.0282277 | intron-variant | NWD1 | GRCh38.p7 | 19:16731296 | AACTGGAAGTCACTC[C/T]GGGCTCCATGCTTTT | 284434 |
rs142166924 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | NWD1 | GRCh38.p7 | 19:16763231 | ACCTAGCCTCTCAGT[C/G]TCTTGCCCTAGTGCA | 284434 |
rs142207002 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | NWD1 | GRCh38.p7 | 19:16760037 | GTACACACTTGTGGT[C/G]CCAGCTACTTGGGAG | 284434 |
rs142223719 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | NWD1 | GRCh38.p7 | 19:16795537 | TTCTCCTGCCTCAGT[A/C]TCCCAAGTATCTGGG | 284434 |
rs142324562 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | NWD1 | GRCh38.p7 | 19:16809664 | GGTTTATGCCATTCT[C/T]CTGCCTCAGCCTCCC | 284434 |
rs142335143 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | NWD1 | GRCh38.p7 | 19:16743273 | TGGAGTGCAGTGGTG[C/T]GATCACAGCTCACTG | 284434 |
rs142368948 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | NWD1 | GRCh38.p7 | 19:16736431 | AGAACGCCCTTCCCT[C/G]TAGTCTGGGTCTGTC | 284434 |
rs142424031 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | NWD1 | GRCh38.p7 | 19:16773543 | TTCTTCTAATGAGCC[C/T]GATGCTAGGGGGTGC | 284434 |
rs142427139 | snp | A/T | 0.000101343 | 0.00711766 | synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749935 | CAGAAACTTCGAGTC[A/T]CTCGTGCTCCTGCTG | 284434 |
rs142432549 | snp | C/G/T | 0.000216786 | 0.0104091 | missense | NWD1 | GRCh38.p7 | 19:16765165 | GCCCTCCAGCTCTGC[C/G/T]GCCCTGCTGTGGAGC | 284434 |
rs142434370 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NWD1 | GRCh38.p7 | 19:16728837 | TAGCCCCAGCTGCTC[A/G]GGAGGCTGAGGCAAG | 284434 |
rs142439584 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16784712 | AAGGTGGGCAGATCA[C/T]GAGGTCAAGAGATCG | 284434 |
rs142507004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16722013 | AGCTACTTGAGACGC[C/T]GAGGCAGGAGGATGG | 284434 |
rs142521652 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NWD1 | GRCh38.p7 | 19:16723696 | TTGTTTTGTTTTGTT[C/T]TGTTTTGTTTTGTTT | 284434 |
rs142546218 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | NWD1 | GRCh38.p7 | 19:16722591 | ACTGTGCCTGGCCGA[C/T]CCTCACTCTTAAAAA | 284434 |
rs142546956 | snp | A/C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16719812 | ATGCCCGGCTAAGCT[A/C/G]GTGCCCTAGTGCAAA | 284434 |
rs142567637 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | NWD1 | GRCh38.p7 | 19:16769969 | CAGCCTCCCAAGTAG[C/G]TGGGACCACAGGTGC | 284434 |
rs142594359 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | NWD1 | GRCh38.p7 | 19:16803109 | CAGGCAAGAGAGTGT[A/G]TGCAGGGGAATTGCC | 284434 |
rs142599900 | in-del | -/AGG | 0.399611 | 0.200291 | intron-variant, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800439 | TTGCGAGGCTGAGGC[-/AGG]AGAATTGTTTGAACC | 284434 |
rs142623081 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | NWD1 | GRCh38.p7 | 19:16745679 | CAGGAGGCAGAGGCT[A/G]TGGTAAGCCAAGATC | 284434 |
rs142661674 | snp | A/G | 6.62471e-05 | 0.00575492 | missense, upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749201 | GAACAGGGAGCCACC[A/G]TCTTCCTTAGAGAGA | 284434 |
rs142667919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16801903 | TAAAAAGAACCTGAC[C/T]CCAGCTACTCAGGAG | 284434 |
rs142669651 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744983 | TTCCTGGCACAGGGG[A/C]CGTATTAGTCTGTTC | 284434 |
rs142675754 | snp | A/G | 9.88354e-05 | 0.00702908 | missense | NWD1 | GRCh38.p7 | 19:16807933 | CTGACGGACTACCGC[A/G]TGGTCTACAGCATGA | 284434 |
rs142696906 | snp | A/C/T | 0.00279242 | 0.0372774 | intron-variant | NWD1 | GRCh38.p7 | 19:16765629 | AGACATGAGCCATGG[A/C/T]GCCTGGCCTAGAATT | 284434 |
rs142710774 | snp | C/T | 0.125874 | 0.217008 | intron-variant | NWD1 | GRCh38.p7 | 19:16727831 | TTTGGGAGGCTGAGG[C/T]GGGTGGATCACTTGA | 284434 |
rs142734109 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | NWD1 | GRCh38.p7 | 19:16814141 | CTCCAGCCTGGGCAA[A/C]AGAGTGAGACCCTGT | 284434 |
rs142741429 | in-del | -/G | 0.0803491 | 0.183626 | intron-variant | NWD1 | GRCh38.p7 | 19:16750911 | CTTAGCCTAGTAAAA[-/G]TCTCGGAGCTATAAA | 284434 |
rs142753074 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16811274 | TTAAGAAATTGAATC[C/T]CCATCGAAAAAAGAA | 284434 |
rs142802641 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | NWD1 | GRCh38.p7 | 19:16767593 | CACTCCAGCCTGGGT[A/G]ACAGAGTGAGACTGT | 284434 |
rs142852841 | snp | C/G | 0.000248639 | 0.0111471 | missense | NWD1 | GRCh38.p7 | 19:16807751 | CCGAGGCCCGGAAAG[C/G]AATCAACTGCATGTC | 284434 |
rs142853739 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16757787 | GGCCAGGTGCAGTGG[C/T]TCACGCCTAATCCCA | 284434 |
rs142872949 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | NWD1 | GRCh38.p7 | 19:16792276 | CTGGGCGCTGTGTCT[A/C]ACTCCTGTAATCCCA | 284434 |
rs142915346 | snp | A/G/T | 9.99574e-05 | 0.00706893 | missense | NWD1 | GRCh38.p7 | 19:16807717 | AATTCCAGGCAGGAC[A/G/T]TGATATGCATTCCCC | 284434 |
rs142921351 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NWD1 | GRCh38.p7 | 19:16766277 | CATGATGGCTTACAC[C/T]TGTAGTCCCAGCTAC | 284434 |
rs142939007 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | NWD1 | GRCh38.p7 | 19:16726050 | TCACTGCAACCTCTG[C/T]CTCCCAGGTTCAAGT | 284434 |
rs142946514 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NWD1 | GRCh38.p7 | 19:16803076 | AAATGAGGAGCAAAG[C/T]CACGTCTTACATGGT | 284434 |
rs142948538 | in-del | -/TATT/TATTTATT/TATTTATTTATT | 0.407798 | 0.270113 | intron-variant | NWD1 | GRCh38.p7 | 19:16734734 | ACCACTACACCTGGC[-/TATT/TATTTATT/TATTTATTTATT]TATTTATTTATTTAT | 284434 |
rs142960783 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | NWD1 | GRCh38.p7 | 19:16811485 | GCTACTTGGGAGGTT[G/T]AGGCAAGAGAATCGC | 284434 |
rs142983651 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16794141 | GAGGCCAAGGTGGGC[A/G]GATCACCTGAGATCA | 284434 |
rs142997351 | snp | A/G | 1.66815e-05 | 0.00288799 | missense | NWD1 | GRCh38.p7 | 19:16773254 | GCACACCCTGTGCTG[A/G]TGCCCCTCGGAGGAT | 284434 |
rs143011868 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16733614 | GTATATTTATTACTA[A/T]GAAAGAAGCAGTGCT | 284434 |
rs143016604 | snp | A/G | 0.0123036 | 0.0774623 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16717973 | CCACCTCAACCTCCC[A/G]AGTAGTTGGGACTAC | 284434 |
rs143023355 | snp | A/G | 1.65274e-05 | 0.00287462 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16791568 | TACCTGTGCCGTCTC[A/G]GTCCAGAAGCAAGGA | 284434 |
rs143037753 | snp | A/G | 8.26043e-05 | 0.00642615 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16791382 | GGAAACTGCAGAGCC[A/G]GTATTCCATATCCTG | 284434 |
rs143070169 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | NWD1 | GRCh38.p7 | 19:16790472 | AAATTCGGGGGGTAG[C/G]GGGTAAGGGGAGGGA | 284434 |
rs143071264 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NWD1 | GRCh38.p7 | 19:16800644 | AGTGCAAGCAGATCT[C/T]GTGTCTGGTGAGGAC | 284434 |
rs143073470 | snp | A/G | 0.00143071 | 0.0267078 | intron-variant | NWD1 | GRCh38.p7 | 19:16763995 | TGGTGACTGCACCAC[A/G]CTCCAGTCTTCTAGA | 284434 |
rs143111258 | snp | A/G | 0.000115358 | 0.0075938 | missense | NWD1 | GRCh38.p7 | 19:16797780 | ACTCGAGGGGCTTTC[A/G]CCGATTCATGGCCAT | 284434 |
rs143157399 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16774387 | CTACCCACCCTGCTA[A/C]CTTTCCATCCATCTA | 284434 |
rs143203258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16769053 | CTTGAAAGCCCAAAA[C/T]GGCCGGGGTGGCTCA | 284434 |
rs143206524 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16752701 | TGGCTTACACTCTAT[A/T]AGAGTACAAATACGG | 284434 |
rs143259044 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16776717 | GAAGATCTCTTGGGC[C/T]GAGATGTTCAAGACC | 284434 |
rs143278325 | in-del | -/ATGCCTATAGACCTAGC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16752512 | ATTTTTTTTAATTAG[-/ATGCCTATAGACCTAGC]CTGAGCATGGTGGTG | 284434 |
rs143381044 | in-del | -/CCACTGC | 0.0193772 | 0.0965046 | intron-variant | NWD1 | GRCh38.p7 | 19:16730675 | TGAGCTATGATTGCA[-/CCACTGC]CCTCCAGCCTGGGTG | 284434 |
rs143401903 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | NWD1 | GRCh38.p7 | 19:16767219 | GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 284434 |
rs143471757 | snp | A/G | 0.000283709 | 0.0119069 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749586 | AGACCTTCTGCGGAC[A/G]CCAGGAACTCCTGGC | 284434 |
rs143480800 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748015 | TTGAGATGGAGTCTC[A/G]CTCTGTTGCACAGGC | 284434 |
rs143485522 | snp | A/G | 8.26098e-05 | 0.00642636 | stop-gained | NWD1 | GRCh38.p7 | 19:16759302 | ATGTGTACCGAGATT[A/G]GACCCCGCCCAGCAA | 284434 |
rs143493948 | snp | C/T | 0.000116491 | 0.00763098 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750130 | GGTGAAGCCCCTTTC[C/T]GGAAACCAAGGCCAG | 284434 |
rs143504850 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16793799 | CCAGGATAGTCTCAA[A/G]CTCCTGACCTCGAGT | 284434 |
rs143526393 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | NWD1 | GRCh38.p7 | 19:16804182 | AGGCTCAGCTAAAGT[A/C]CCTCTCAGCATCATT | 284434 |
rs143565675 | snp | C/G/T | 0.000202427 | 0.0100586 | missense | NWD1 | GRCh38.p7 | 19:16750245 | TGTGGGAACCCAGGG[C/G/T]GGCTGAGGCTGGCGT | 284434 |
rs143568772 | snp | C/G | 0.0271762 | 0.113356 | intron-variant | NWD1 | GRCh38.p7 | 19:16727252 | GAGGAGCTGGGAAGA[C/G]GACTCCCGTGCCTAG | 284434 |
rs143588989 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16757148 | GCACTTGATCATCCC[A/C]AAACCATCACCCCTA | 284434 |
rs143589588 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NWD1 | GRCh38.p7 | 19:16755292 | GCGATCACAGCTCGC[C/T]GCAGTCTTGACTTCT | 284434 |
rs143623483 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16753936 | CCATCATCTCAATCC[G/T]CCATCCTTCCATCCA | 284434 |
rs143637677 | snp | A/C | 0.000153988 | 0.00877328 | utr-variant-3-prime, missense | NWD1 | GRCh38.p7 | 19:16815055 | CAGTCCAGTTTGTCC[A/C]TGCTGTGGTAAACAG | 284434 |
rs143678357 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16746711 | AAAAAAACAGTCGAT[A/G]AACACATATTTTGCA | 284434 |
rs143682457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16806488 | ACTTTGGGAGGCAAA[A/G]GTGGGAGGATCGTTT | 284434 |
rs143704868 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NWD1 | GRCh38.p7 | 19:16786228 | TGCCCGGCTTGTCTC[A/G]GACTCCTGGGCTCAA | 284434 |
rs143795871 | snp | A/C/G | 0.000162531 | 0.00901338 | missense | NWD1 | GRCh38.p7 | 19:16750386 | CTCCTCGTGGCCCAC[A/C/G]TGCTGGGCTACATTG | 284434 |
rs143820605 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | NWD1 | GRCh38.p7 | 19:16722255 | AGTGAGCCACAATAG[C/T]GCCACTGCACTCCAG | 284434 |
rs143822519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16739599 | GAACCAGGCATCACC[C/T]CTCTACTGCCCAAGA | 284434 |
rs143824559 | snp | A/G | 3.41904e-05 | 0.00413449 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16789187 | TTCAGCATCTGGCTC[A/G]AAGGTAACAAACATA | 284434 |
rs143828678 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | NWD1 | GRCh38.p7 | 19:16797372 | GTCTGGCTCTGTTGC[A/C]CAGGCTGGAGTGTAG | 284434 |
rs143856587 | in-del | -/TGAC | 0.213937 | 0.247385 | intron-variant | NWD1 | GRCh38.p7 | 19:16785585 | AAAGAAAAAAGAGGA[-/TGAC]TGTTTTCTGAGATTA | 284434 |
rs143860252 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16740001 | CCTGAAACTGACTAG[G/T]TATAAAGAGATGAGG | 284434 |
rs143872492 | snp | C/T | 0.000181253 | 0.00951808 | stop-gained, synonymous-codon | NWD1 | GRCh38.p7 | 19:16797782 | TCGAGGGGCTTTCGC[C/T]GATTCATGGCCATGG | 284434 |
rs143890689 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16736867 | CTTTCGTACCTTATC[C/T]CTATGGCCTGCCTGT | 284434 |
rs143893605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16771218 | ATACTTTGAGAAGCC[A/G]AGGCAGGCAGATTGC | 284434 |
rs143901094 | snp | A/G | 0.030278 | 0.119257 | intron-variant | NWD1 | GRCh38.p7 | 19:16725656 | CTCCCAGGTTCAAGC[A/G]ATGCTTCCGCCTCAG | 284434 |
rs143908337 | snp | A/C/T | 0.000609702 | 0.0174507 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807836 | GCTGGACATCACCTC[A/C/T]GGGGACCCCTGCCCG | 284434 |
rs143989460 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | NWD1 | GRCh38.p7 | 19:16784536 | CCTCCCAGGCACAGG[A/G]AGCAGCAAGTGCAAA | 284434 |
rs144006927 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16742511 | GTGACCTTGGACTAA[C/T]TCTGTTCCATCCCCA | 284434 |
rs144013868 | snp | A/G | 0.00267098 | 0.0364466 | missense | NWD1 | GRCh38.p7 | 19:16807738 | TGCATTCCCCCTCCC[A/G]AGGCCCGGAAAGCAA | 284434 |
rs144054207 | snp | A/G | 0.00194575 | 0.0311302 | missense | NWD1 | GRCh38.p7 | 19:16761992 | AGACAGCTGGTCGAG[A/G]TGGTCCGTGAGCGCT | 284434 |
rs144172607 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732617 | TTTTTTTTTTTTTCA[A/G]ATGAGGTCCAGTGGA | 284434 |
rs144216743 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16729644 | GTACTTTAGGGGGCC[A/G]AGGCACCTGAGGTGA | 284434 |
rs144229379 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | NWD1 | GRCh38.p7 | 19:16785930 | AGTGCAATGACATGA[A/T]CTTGGCTCCCTGCAA | 284434 |
rs144260858 | in-del | -/AAGG | 0.0637235 | 0.166737 | intron-variant | NWD1 | GRCh38.p7 | 19:16751983 | AAGAAGAAAAAGTGA[-/AAGG]AAGGAAGGAAGGAAG | 284434 |
rs144261429 | snp | C/G | 1.65258e-05 | 0.00287448 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749288 | CTCGCGGATGGCTGC[C/G]TGGACGCTGATGCCC | 284434 |
rs144266347 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816860 | GTTCTGCAAATGTTA[A/G]TGTCAAATTTCATTT | 284434 |
rs144268436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16782322 | GTGTTTTAAATTAGC[C/T]AGGCATGGTGGTGTG | 284434 |
rs144278148 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16760969 | TGTCTAGTTCCAGAA[A/C/T]GTTTTCATCTCCCCA | 284434 |
rs144292032 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NWD1 | GRCh38.p7 | 19:16720684 | CTCAGCCTCCTGAGT[A/G]GCTGGGACTACAGGT | 284434 |
rs144307501 | in-del | -/TCTT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782871 | TTTTCCTTCTTTCTT[-/TCTT]TCTTTCTTTCTCTTT | 284434 |
rs144308827 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NWD1 | GRCh38.p7 | 19:16813103 | ATACAGCCATCCTTC[C/T]GAGGATAGACTGGGC | 284434 |
rs144364062 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | NWD1 | GRCh38.p7 | 19:16728710 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCGAATCA | 284434 |
rs144404078 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16734216 | ACACGTCCTTGCTTT[C/G]AAAGCAACAGTTTGA | 284434 |
rs144445491 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NWD1 | GRCh38.p7 | 19:16765415 | CGTAGCTCACTGTAG[C/T]CTCAGACTCCTGGGT | 284434 |
rs144449044 | snp | A/G | 0.000153988 | 0.00877328 | missense | NWD1 | GRCh38.p7 | 19:16779449 | GCATGTGATCCACAT[A/G]CTAACTGGACACACA | 284434 |
rs144449795 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16731717 | TCAAGCGATTCTCTC[A/G]CCTCAGCCTCCTGAG | 284434 |
rs144454769 | in-del | -/AGGGA | 0.0271762 | 0.113356 | intron-variant | NWD1 | GRCh38.p7 | 19:16777695 | GGAAGGAGAAAGGGG[-/AGGGA]AGGGAAGGGAAGGGG | 284434 |
rs144463947 | snp | C/T | 0.00024707 | 0.0111119 | missense | NWD1 | GRCh38.p7 | 19:16789048 | CTTCAAAGGATTACA[C/T]GCTGCACTTGTGGAA | 284434 |
rs144467750 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16747793 | TGCCTGTTCTGGACA[C/T]TTCATGTCAATGGAA | 284434 |
rs144581856 | in-del | -/C | 0.161596 | 0.233848 | intron-variant | NWD1 | GRCh38.p7 | 19:16746676 | GACTCTGTCTAAAAA[-/C]AAAAAACAAAAAACA | 284434 |
rs144616905 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16723590 | GTGCCGAGATTACAG[G/T]CATGAGCCACTGTGC | 284434 |
rs144637791 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16798305 | TGAGCTATTTTTTCC[A/C]GTTTTAAAGAAATTG | 284434 |
rs144686652 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16762734 | AGGCTGGAGGCAGGA[C/T]CAGGCTCTATTCTTT | 284434 |
rs144709772 | in-del | -/TCCTTCCTTCCTTCTTTCCTTCCTT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782899 | CTCTTTCTTTTTCCA[-/TCCTTCCTTCCTTCTTTCCTTCCTT]TCCTTCCTTCCTTCC | 284434 |
rs144723529 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | NWD1 | GRCh38.p7 | 19:16761475 | TCCACCTGGGAGGAG[A/T]GATTCTCCTGCCTCA | 284434 |
rs144729143 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | NWD1 | GRCh38.p7 | 19:16792009 | ATGAGCCACCGTGCC[C/T]GGCCACACGCTTGGC | 284434 |
rs144738302 | snp | A/G | 0.111224 | 0.207945 | intron-variant | NWD1 | GRCh38.p7 | 19:16743668 | CATATTTATTTATTT[A/G]TTTATTAGTTTGTTT | 284434 |
rs144760676 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | NWD1 | GRCh38.p7 | 19:16752798 | GCCCAGGAGTTCAAG[A/C]CCAGCCTGGGCAACA | 284434 |
rs144804746 | snp | A/G | 0.000206292 | 0.010154 | missense | NWD1 | GRCh38.p7 | 19:16759386 | GATACTACTTGGCCC[A/G]GCGGCCCGTGGATGG | 284434 |
rs144808399 | snp | A/C/T | 0.000610783 | 0.017465 | synonymous-codon, missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749270 | CTTAGGATGGTGGAC[A/C/T]GGCTCGCGGATGGCT | 284434 |
rs144819630 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16723847 | ATTACAGACGTGCAC[C/T]GTCATGCCCGGCTAA | 284434 |
rs144830696 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NWD1 | GRCh38.p7 | 19:16809891 | TCCAACTGATACTTA[C/T]TGAAAAACCTCTGCC | 284434 |
rs144849244 | snp | A/G | 0.000204394 | 0.0101072 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749637 | GGCACGATGACAGCA[A/G]GCAGCACACCCCCCT | 284434 |
rs144850445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16722093 | ACTCTAATCTGGGCA[A/G]TGGAGTGAGACCCTG | 284434 |
rs144865335 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16808763 | CAGGCATGACCCACC[A/G]GACCTGGCTACAAAG | 284434 |
rs144868602 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | NWD1 | GRCh38.p7 | 19:16807285 | GATCACCTGAGGTTG[A/G]GAGTTAGAGACCAGC | 284434 |
rs144904456 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | NWD1 | GRCh38.p7 | 19:16805901 | TGAGAGGGAGTTTCC[A/G]TCTGTTGCCCGGGCT | 284434 |
rs144906792 | in-del | -/TCCA | 0.461991 | 0.132514 | intron-variant | NWD1 | GRCh38.p7 | 19:16754463 | CCATCATCTCTATTT[-/TCCA]TCCATCCATCCATCC | 284434 |
rs144954606 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | NWD1 | GRCh38.p7 | 19:16721915 | CAAGAGTTCAAGAAC[A/G]GCCTGAGCAACACAG | 284434 |
rs144961672 | snp | C/T | 0.000116199 | 0.00762142 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16773238 | CTGGTTCCAGTTGTG[C/T]GCACACCCTGTGCTG | 284434 |
rs144979257 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | NWD1 | GRCh38.p7 | 19:16730061 | GGGCGCAGTGGCTCA[C/T]GCCTGTGATCCCAGC | 284434 |
rs145011343 | snp | C/T | 3.2975e-05 | 0.00406035 | missense | NWD1 | GRCh38.p7 | 19:16763859 | TGTGGTTCTCACATA[C/T]GGTTGCAAACCTGCG | 284434 |
rs145038286 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749239 | CCTCCACAAACACAT[C/T]CTTGAAGACTGCGCC | 284434 |
rs145039514 | in-del | -/TCTT | 0.144296 | 0.226554 | intron-variant | NWD1 | GRCh38.p7 | 19:16761350 | TGTTCCCTTTCTTTC[-/TCTT]TCTTTCTTTCTTTCT | 284434 |
rs145077526 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | NWD1 | GRCh38.p7 | 19:16737699 | GAGCAGGGGGCCGGG[C/T]GTGGTGGCTCACACC | 284434 |
rs145099830 | in-del | -/TT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782861 | CTTTCTTCCTTTTCC[-/TT]TTCTTTCTTTCTTTC | 284434 |
rs145127193 | snp | A/C | 1.64849e-05 | 0.00287092 | missense | NWD1 | GRCh38.p7 | 19:16791531 | GGAAGCAACATATGT[A/C]CAGCATCAAAGAAGA | 284434 |
rs145131372 | snp | A/G | | | synonymous-codon | NWD1 | GRCh38.p7 | 19:16759309 | CCGAGATTGGACCCC[A/G]CCCAGCAAGGAGCTG | 284434 |
rs145134407 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16796272 | TGATCTGAACTTCTG[A/T]TGATCATGGTGAAAC | 284434 |
rs145151472 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748930 | TGCAAATGCAAACTC[C/T]GGGGCCCCACTCAGA | 284434 |
rs145266010 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NWD1 | GRCh38.p7 | 19:16795318 | CCAGGCTCCATGCAG[A/G]GCCCATGGGCAGACC | 284434 |
rs145279920 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16734774 | TATTTATTGTAGACA[C/T]AATGTCTCCCTATAT | 284434 |
rs145282223 | snp | C/G/T | 0.0135052 | 0.0812326 | intron-variant | NWD1 | GRCh38.p7 | 19:16792479 | GTTGGGAGTTCGAGA[C/G/T]CAGCCTGGCCAACAT | 284434 |
rs145308533 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | NWD1 | GRCh38.p7 | 19:16805330 | TCCCAAAGTGCTAGG[A/G]TTACAGGTGTGCACC | 284434 |
rs145318617 | snp | A/C | 0.126909 | 0.217598 | intron-variant | NWD1 | GRCh38.p7 | 19:16738730 | ACATATATATATAAT[A/C]TATATATAATATATA | 284434 |
rs145420132 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16724040 | CTAAGGAATCATGGA[A/G]CTTGAGGGTGCTCTT | 284434 |
rs145500844 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16782950 | TTCCCTTCCTTCCCC[C/T]CTTCCCCTTCCTCCC | 284434 |
rs145522776 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16744197 | AGTTCAATACCAGCC[C/T]GGGTAATGTAGTGAG | 284434 |
rs145543702 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NWD1 | GRCh38.p7 | 19:16779063 | AACCGATATGTGTCC[A/G]CTGGGTGAGCACTGC | 284434 |
rs145594463 | snp | C/T | 0.000281373 | 0.0118578 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744463 | TGTCTGATTCCCTCG[C/T]GGATCGATGAGAAGG | 284434 |
rs145613435 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16765514 | AATTTTTCTATTTTT[C/T]GTAGAGACAGGGTCT | 284434 |
rs145633327 | snp | A/G | 0.0744748 | 0.178019 | intron-variant | NWD1 | GRCh38.p7 | 19:16776330 | ATCCCAGCGCTTTGG[A/G]AGGTTGAGGCAGGTG | 284434 |
rs145641467 | snp | A/G | 0.000116278 | 0.00762401 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749504 | GAGCTGGATACGGCC[A/G]GACAGGAGTTGGCGT | 284434 |
rs145666110 | snp | A/G | 0.00045129 | 0.0150147 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750169 | CCAACTCCTGCTGGC[A/G]GCTGCAAGGAGGACG | 284434 |
rs145672105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16726589 | GGATTACAGGCCTGC[A/G]CCACCACACCTGGCT | 284434 |
rs145688630 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | NWD1 | GRCh38.p7 | 19:16782084 | GGGCGACAGAGTGAG[A/G]CTCTGTCTCAAAAAA | 284434 |
rs145692852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16724846 | TACAGGCATGTGACA[C/T]CATACCCAGCTAATT | 284434 |
rs145720941 | snp | A/G | 0.000527148 | 0.0162264 | missense | NWD1 | GRCh38.p7 | 19:16789119 | GGCTCAAAAAATCCC[A/G]CTGAACCTCAGATCT | 284434 |
rs145815626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16755976 | ATAGCCTACTGTTGA[C/T]CAGAAGCCTTACCAG | 284434 |
rs145840364 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16766884 | AACCACTGTGCCTGA[A/C]CCCCATCTTAACCAT | 284434 |
rs145845607 | snp | C/T | 8.23676e-05 | 0.00641693 | missense | NWD1 | GRCh38.p7 | 19:16807922 | GCGTGGCCATTCTGA[C/T]GGACTACCGCGTGGT | 284434 |
rs145878461 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | NWD1 | GRCh38.p7 | 19:16763491 | TCCAGACCTTTGCCC[A/G]TGCTGTTCCCTTGCC | 284434 |
rs145927111 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16801953 | TTGAGGCCGGGAGTT[C/G]AAGACCAGCCTGGGC | 284434 |
rs145955690 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16762048 | GAGGCATGGCGTCCT[A/G]GCCGACTTCTTCTCA | 284434 |
rs146011178 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16722613 | TCTTAAAAAAGAATT[A/G]ACTCAGCAGGCCTGA | 284434 |
rs146038099 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16804754 | CTCTTTCTGGGTCAT[A/G]GATGGCCAGATTTTC | 284434 |
rs146047131 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | NWD1 | GRCh38.p7 | 19:16788284 | AATAATAATAATAAT[A/G]AAAGGCCAGGCATGG | 284434 |
rs146091518 | in-del | -/TA | 0.0973687 | 0.197999 | intron-variant | NWD1 | GRCh38.p7 | 19:16785801 | TATATAAATATATAC[-/TA]TATATATATATTTTT | 284434 |
rs146101403 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16730410 | TAAGCATAAGGGGTA[C/G]AATGGCAAACAAGAT | 284434 |
rs146121969 | snp | A/G | 0.00963404 | 0.0687329 | missense | NWD1 | GRCh38.p7 | 19:16773311 | CGGGCAACTCTCAGC[A/G]GCTGTCACAAAGGTG | 284434 |
rs146147636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16756900 | ATTAGATTCTCATAA[A/G]AGCACAAACCTTGTT | 284434 |
rs146179167 | snp | C/G | 0.123452 | 0.215605 | intron-variant | NWD1 | GRCh38.p7 | 19:16758868 | CAAAAATTAGCCAGG[C/G]GTGGTGGCGCCTGTA | 284434 |
rs146259101 | in-del | -/TCTTCTGTCCG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764385 | CCATCCATCCATCCA[-/TCTTCTGTCCG]TCCATCCATCCATCC | 284434 |
rs146267567 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16743684 | TTTATTAGTTTGTTT[A/G]TTTATTTATTTATTT | 284434 |
rs146271791 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800426 | GTATCCCCAGCTACT[C/T]GCGAGGCTGAGGCAG | 284434 |
rs146279608 | snp | G/T | 0.0644693 | 0.167566 | intron-variant | NWD1 | GRCh38.p7 | 19:16742046 | ATTGTACCACTGCAC[G/T]CCAGCCTGGGTGACA | 284434 |
rs146289351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16757252 | CTACAACACACAGGA[C/T]GGTCCCCACCCTAAA | 284434 |
rs146291620 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815457 | CTTCAGATTATGGCT[C/T]CAGACCTTGTCTCTT | 284434 |
rs146432139 | snp | A/C/T | 0.000337851 | 0.0129932 | synonymous-codon, stop-gained | NWD1 | GRCh38.p7 | 19:16765183 | CCTGCTGTGGAGCTC[A/C/T]GAGGCATGGGTGAGT | 284434 |
rs146450477 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | NWD1 | GRCh38.p7 | 19:16742635 | TAGAATGGAGAACCA[A/C]CACAAGATTTAATTT | 284434 |
rs146451489 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | NWD1 | GRCh38.p7 | 19:16743296 | GCTCACTGCAGCCTC[A/G]AACTCCTGAGCTCAA | 284434 |
rs146462547 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | NWD1 | GRCh38.p7 | 19:16738805 | ATAACATATAACATA[C/T]TATTATATGTATAAT | 284434 |
rs146464810 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16795940 | CTAAGCTCTTGTCCC[A/G]TGTCCAAGAAGAATG | 284434 |
rs146522638 | snp | A/G | 0.0260105 | 0.111035 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718808 | GCTGGGATTACTGGC[A/G]TGAGCCACCATGCCT | 284434 |
rs146553378 | snp | G/T | 0.0132985 | 0.0804513 | missense | NWD1 | GRCh38.p7 | 19:16807782 | CCTGAGCAAGTGCGA[G/T]GACCGCCTGGCCATC | 284434 |
rs146575213 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | NWD1 | GRCh38.p7 | 19:16786106 | CTGACCTCAACTGAT[A/T]CACCCACCTTGGCCT | 284434 |
rs146583551 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | NWD1 | GRCh38.p7 | 19:16727078 | GCTGTGGGGCTGGGC[A/G]TGGCTCCCAGCCTCT | 284434 |
rs146587068 | snp | A/G | 0.00636936 | 0.0560724 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817329 | AATGGCAAAAGCCTC[A/G]GTGGCTCACGCCTGT | 284434 |
rs146587590 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16782357 | TGAAGTCCCAGCTAC[A/G]TGAGAGGCTGAGCCA | 284434 |
rs146642041 | in-del | -/AG | 0.0383715 | 0.133092 | intron-variant | NWD1 | GRCh38.p7 | 19:16777904 | GGGAAGGAAAGAGAA[-/AG]GGGAGGGGAAGGAAA | 284434 |
rs146651353 | snp | C/T | 0.000570396 | 0.0168782 | intron-variant | NWD1 | GRCh38.p7 | 19:16738216 | GTATTGACTGTCTGA[C/T]TTTTTCCAGGAGAAA | 284434 |
rs146675556 | in-del | -/C | 0.0236746 | 0.106192 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816685 | TAATGCTAGGATAGT[-/C]TAAATCTTCAAGGTG | 284434 |
rs146692736 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | NWD1 | GRCh38.p7 | 19:16769332 | CCAGGCACGGTAGCA[C/T]GCACCTGTAATCCCA | 284434 |
rs146703380 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16766486 | CTGCAATTTGCTACT[A/C]CCTGCCCTAGAGCTT | 284434 |
rs146716518 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16813156 | CTCAGGAGTAGCCAT[A/G]GGGTGGTATGGATGG | 284434 |
rs146719346 | in-del | -/ATATATAATATATA | 0.39198 | 0.205771 | intron-variant | NWD1 | GRCh38.p7 | 19:16738769 | ATATATAATATAATG[-/ATATATAATATATA]ATATATAATAACATA | 284434 |
rs146771693 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | NWD1 | GRCh38.p7 | 19:16726518 | GATCTTAGTTCACTG[C/T]AACCTCCACCTCCTG | 284434 |
rs146780952 | snp | C/T | 0.00087278 | 0.0208717 | utr-variant-3-prime, synonymous-codon | NWD1 | GRCh38.p7 | 19:16815101 | CAGTGGCTTCATTGC[C/T]CCCACCAGGCATGGT | 284434 |
rs146813620 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16754396 | CATCATCTCTATCTT[C/G]CATCCATCTATCCAT | 284434 |
rs146813753 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16724454 | TCCAACCAGGCTCAC[A/G]GATGCCAAGGTATAC | 284434 |
rs146827871 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | NWD1 | GRCh38.p7 | 19:16809799 | CCTGACCTCGTGATC[C/T]GCCCACCTTGGCCTC | 284434 |
rs146882465 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16729331 | CTGTCATATCCACAC[C/G]AGAATCCATAGATCC | 284434 |
rs146889704 | snp | A/G | 0.00011537 | 0.00759418 | missense | NWD1 | GRCh38.p7 | 19:16807837 | CTGGACATCACCTCC[A/G]GGGACCCCTGCCCGG | 284434 |
rs146905478 | snp | C/T | 0.0112041 | 0.0740036 | intron-variant, missense | NWD1 | GRCh38.p7 | 19:16745064 | GAGGTTTAATGGACT[C/T]ACAATTCCACATGGC | 284434 |
rs146942210 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16730521 | GAGTCTGAGGCCAGC[A/C]TAGAAAACATAGTGA | 284434 |
rs146943338 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | NWD1 | GRCh38.p7 | 19:16787093 | CCTTCCAAATTGTAC[A/G]TTTTGCTTAGCAAAT | 284434 |
rs146963139 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NWD1 | GRCh38.p7 | 19:16814381 | CTCCTATAGAAAAGG[C/T]GCTCATTGTGTATTA | 284434 |
rs147010150 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16732313 | AGTGAGTAGGAGTGA[A/G]TGCTTTTGAACACAG | 284434 |
rs147012763 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NWD1 | GRCh38.p7 | 19:16790100 | ATTACATCAATCATA[A/G]CCCTGTGATTTCATA | 284434 |
rs147047001 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16720066 | TGACACTGCAAAGGG[A/C]CTCTGTCCTTACTGG | 284434 |
rs147048038 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16770733 | GAACCTCCACCCGTG[C/T]TGCCATCGAGGGTCC | 284434 |
rs147054413 | snp | A/G | 5.20648e-05 | 0.00510193 | missense | NWD1 | GRCh38.p7 | 19:16750348 | ACCAACTCTGCACCC[A/G]CCTGGAGCAGACACA | 284434 |
rs147057896 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | NWD1 | GRCh38.p7 | 19:16803672 | CTGTAATCCCAGAAC[A/T]TTGGGAGGCTGAGGT | 284434 |
rs147064227 | snp | A/G | 0.000149094 | 0.00863278 | missense | NWD1 | GRCh38.p7 | 19:16763934 | TGGAGGAGCTGAAAC[A/G]GGAGGTTCTGGGTAA | 284434 |
rs147067929 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NWD1 | GRCh38.p7 | 19:16800900 | AGCACTCTGGGAGGC[C/T]GAGGCAGTAGGATTG | 284434 |
rs147107714 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NWD1 | GRCh38.p7 | 19:16743071 | CTGCACGCCACCATG[C/T]CTGGCTAATTTTTGT | 284434 |
rs147119646 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16735864 | GGAAGGAAGGAAGGA[A/G]GGAGGAAGGAAGGAA | 284434 |
rs147149886 | snp | C/G | 0.000221373 | 0.0105184 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807680 | GGGCCTCGTGTCGGG[C/G]GTCGTCCTTGTGTTC | 284434 |
rs147170721 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748132 | GGGATTACAGGCGTG[C/T]GGCATCACGCTGGGC | 284434 |
rs147217509 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | NWD1 | GRCh38.p7 | 19:16795395 | AAGCCCCAGAGGGGG[A/T]GTTACAGTGTGCTAA | 284434 |
rs147219947 | in-del | -/ATA | 0.0310518 | 0.120672 | intron-variant | NWD1 | GRCh38.p7 | 19:16766162 | GATGAAATTCAAAAT[-/ATA]ATAATAACTGAGTAC | 284434 |
rs147243582 | snp | A/G | 1.86e-05 | 0.00304953 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750403 | GCTGGGCTACATTGT[A/G]TCTTCCCGGTAAGTC | 284434 |
rs147277505 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16736955 | CATTAGCAGTCAAAT[A/G]GAAGCAGCAGGTGGC | 284434 |
rs147278608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16795075 | AGGCGTGAGCCATTG[C/T]GCCCAGCCCTTTCTT | 284434 |
rs147286781 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | NWD1 | GRCh38.p7 | 19:16784657 | AGCAGTCGGCTGGGC[A/G]CGGTGGCTCACGCCT | 284434 |
rs147323422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16780579 | AGAGCAGTCCAGTAG[A/G]GAAATAGGCTAAATA | 284434 |
rs147373236 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16727951 | CCTGTAATCCCAGCT[A/G]CTTGAGAGGCTGAGG | 284434 |
rs147382889 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16726025 | TGGAGTGCAGTGGCA[C/T]GATCTTGGCTCACTG | 284434 |
rs147384882 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16780195 | GAGTCTTGCTCTGTC[A/G]CCCAAGCTAGAGTGC | 284434 |
rs147414453 | in-del | -/A | 0.0733688 | 0.176922 | intron-variant | NWD1 | GRCh38.p7 | 19:16773810 | TCCATCCTTTCATTC[-/A]CCTTCCTACTCTTCC | 284434 |
rs147419023 | snp | A/C | 0.000349066 | 0.0132065 | missense | NWD1 | GRCh38.p7 | 19:16807733 | TGATATGCATTCCCC[A/C]TCCCGAGGCCCGGAA | 284434 |
rs147476006 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718097 | CTGGCCTTGAGTGAT[A/C]CTCCCACCTTGGCTT | 284434 |
rs147478618 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16767474 | ACAAAAATTTGTCAG[A/G]CGTGGTGGCACATGC | 284434 |
rs147489023 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16764768 | TCTGCCCCCCCAGGG[C/G]ACACTTGACAATGTC | 284434 |
rs147535093 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16809047 | GGTGATAGAGCAAGG[A/C]CTGTCTCAAGAAAAC | 284434 |
rs147553604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16790372 | TTACATAAGTAATTG[A/G]TGGTTGTTGACAGTA | 284434 |
rs147639383 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782890 | TCTTTCTTTCTCTTT[C/T]TTTTTCCATCCTTCC | 284434 |
rs147640381 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16758568 | AGGTGTGAGCCACCA[C/T]GCCCAGCCCAATTAT | 284434 |
rs147650019 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | NWD1 | GRCh38.p7 | 19:16792526 | TACTAAAAAAGCATA[C/T]AAAAAATTAGCCGGG | 284434 |
rs147707617 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16746548 | CATGGTGGTGCACAC[C/T]TGTAGTCCCAGCTAC | 284434 |
rs147713373 | in-del | -/GAAAA/GAAAAGAAAA/GAAAAGAAAAGAAAAGCAAA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16737964 | GCAAGACTCTATCTC[lengthTooLong]GAAAAGAAAAGAAAA | 284434 |
rs147723042 | snp | C/T | 0.000315565 | 0.0125572 | synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749527 | GTTGGCGTGGCTCTA[C/T]CAAGAGATCCGCCAC | 284434 |
rs147743532 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744886 | TTTACTGATCCAAGA[A/T]AGTTCAGCCATGTTC | 284434 |
rs147804464 | in-del | -/GCATGCCTATAGACCTA | 0.333261 | 0.235728 | intron-variant | NWD1 | GRCh38.p7 | 19:16752526 | GCTGAGCATGGTGGT[-/GCATGCCTATAGACCTA]GCTACTCCGGAGGCT | 284434 |
rs147828282 | snp | A/G/T | 0.000197724 | 0.00994109 | missense, stop-gained, synonymous-codon | NWD1 | GRCh38.p7 | 19:16797842 | GCTGTTTTTGGTACT[A/G/T]AGAACAACCTGATCA | 284434 |
rs147856994 | snp | C/T | 6.59946e-05 | 0.00574395 | missense | NWD1 | GRCh38.p7 | 19:16761998 | CTGGTCGAGGTGGTC[C/T]GTGAGCGCTACCTGT | 284434 |
rs147869133 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16803193 | TGGGGGAGACTGCCT[C/G]CATGATTCAATTATC | 284434 |
rs147917808 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16723907 | CACCATGTTGGCCGC[A/G]CTGGTCTCCGACTCC | 284434 |
rs147918682 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16776075 | TATGGGGGCACAAAT[C/T]GCACATAGTGCTGTG | 284434 |
rs147945927 | in-del | -/TTCTTTCC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16783009 | TCTCTCTCTCTTTCT[-/TTCTTTCC]TTCTTTCCTTCTTTC | 284434 |
rs147952603 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | NWD1 | GRCh38.p7 | 19:16722205 | TCAGGAGGCTGAGGT[A/G]GGAGGATCACTTGAG | 284434 |
rs147955578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16773705 | CAGCCCTTGGAATCC[C/T]AGAATGTAAGGGAGA | 284434 |
rs147984852 | snp | C/T | 0.00282082 | 0.0374494 | missense | NWD1 | GRCh38.p7 | 19:16808107 | TGGGACCTGCAGGCA[C/T]GCAAGTGGAAATTCG | 284434 |
rs148007496 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | NWD1 | GRCh38.p7 | 19:16730732 | TAAAAAACATTTTTT[A/T]AAAAATATATACAGG | 284434 |
rs148016030 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | NWD1 | GRCh38.p7 | 19:16759758 | TTAGCACTTTGGGAG[G/T]CTGAGGTGGCGGATC | 284434 |
rs148020552 | snp | A/G | 0.000248289 | 0.0111392 | missense | NWD1 | GRCh38.p7 | 19:16807649 | AGGTTGCTGAGCAGC[A/G]CAAGCTCCTATTTAC | 284434 |
rs148025609 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | NWD1 | GRCh38.p7 | 19:16720703 | GGGACTACAGGTGTC[C/T]GCCACATGCCCGGCT | 284434 |
rs148027502 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16771959 | CGCGCCACCATGCTC[A/G]GCTAATTTTTCTTAA | 284434 |
rs148029259 | snp | A/G | 0.00131623 | 0.02562 | missense | NWD1 | GRCh38.p7 | 19:16750273 | CGTTTGAGGAAGCCC[A/G]GAAATGGGCCTCTTT | 284434 |
rs148036796 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16804451 | AAATTTAAAAGGTAT[C/G/T]GGGCTTGGTGGTACA | 284434 |
rs148067405 | snp | C/T | 0.000461422 | 0.0151822 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16808064 | GCAGCTGGTGGTCAG[C/T]GGGTCTGAGGATGCC | 284434 |
rs148074525 | in-del | -/GAGGTTGCAGTGAGCC | 0.100231 | 0.200173 | intron-variant | NWD1 | GRCh38.p7 | 19:16784862 | TGAACCCGGGGGGCG[-/GAGGTTGCAGTGAGCC]GAGATCGCGCCACTG | 284434 |
rs148076364 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | NWD1 | GRCh38.p7 | 19:16722256 | GTGAGCCACAATAGT[A/G]CCACTGCACTCCAGC | 284434 |
rs148080078 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16797497 | CACCACACCTGGCTA[A/C]TTTTTGTATTTTTAG | 284434 |
rs148176553 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | NWD1 | GRCh38.p7 | 19:16763699 | TGGGCACATGGGGGT[A/C]TGTCTGTCTTCCATT | 284434 |
rs148230637 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | NWD1 | GRCh38.p7 | 19:16790794 | AAGTGATACCACTTG[G/T]ACATATTAGGTTGAA | 284434 |
rs148240680 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | NWD1 | GRCh38.p7 | 19:16800901 | GCACTCTGGGAGGCC[A/G]AGGCAGTAGGATTGT | 284434 |
rs148288566 | snp | C/G | 0.0303148 | 0.119325 | intron-variant, missense | NWD1 | GRCh38.p7 | 19:16745081 | CAATTCCACATGGCT[C/G]GGGAGGCCTCACAAT | 284434 |
rs148291568 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | NWD1 | GRCh38.p7 | 19:16767294 | ATGCATGGCAGCAGG[A/C]GAGAGAGAGGGAGCA | 284434 |
rs148295009 | snp | C/T | 0.000297432 | 0.0121913 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16773172 | CAGACTCCATTTCTT[C/T]GCCACCTCACATCCA | 284434 |
rs148328721 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16761542 | TGTATTCTTTTTTTT[-/T]AGTACAGACAGGGTT | 284434 |
rs148385342 | snp | G/T | 0.0494327 | 0.149241 | intron-variant | NWD1 | GRCh38.p7 | 19:16736364 | CCTCCCGAGTAGCTG[G/T]GACTACAGGTGCCCA | 284434 |
rs148394779 | snp | C/T | 4.94238e-05 | 0.00497086 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16789022 | TGCCAAAGGGACCCT[C/T]GCCAACTCTGCTTCA | 284434 |
rs148398303 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | NWD1 | GRCh38.p7 | 19:16798364 | CCTGTAATCCCAGCA[C/T]TTTGGAAGGCCAAGG | 284434 |
rs148404229 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16747882 | GTTCATCCACATTTT[A/C]ACACCTGTGAGTACT | 284434 |
rs148477404 | in-del | -/TTTATTTA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16747346 | GGCTGACATTTTCTT[-/TTTATTTA]TTTATTTATTTATTT | 284434 |
rs148511125 | in-del | -/CATC | 0.298905 | 0.24517 | intron-variant | NWD1 | GRCh38.p7 | 19:16753829 | CTCCATCATCTCTAT[-/CATC]CATCCATCCATCCAT | 284434 |
rs148541287 | snp | C/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718148 | GGAGCATGCCACTGT[C/G]CCTGGCAGCACCTGA | 284434 |
rs148542774 | snp | A/G | 0.000153988 | 0.00877328 | missense | NWD1 | GRCh38.p7 | 19:16807745 | CCCCTCCCGAGGCCC[A/G]GAAAGCAATCAACTG | 284434 |
rs148546939 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16792017 | CCGTGCCCGGCCACA[C/T]GCTTGGCTTCTTAAT | 284434 |
rs148603782 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16745841 | AGGATCGCTGGAGCC[C/T]GGGAGTTGGAGGCTG | 284434 |
rs148604193 | in-del | -/TTCACCATGTTGGCCAGGC | 0.0123036 | 0.0774623 | intron-variant | NWD1 | GRCh38.p7 | 19:16813671 | GAGTAGAGGTAGGGT[-/TTCACCATGTTGGCCAGGC]TGGTCTTGAACTCCT | 284434 |
rs148613755 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NWD1 | GRCh38.p7 | 19:16779780 | TAGCTGGGACTACAA[A/G]CACATACCACTATAC | 284434 |
rs148701796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16737700 | AGCAGGGGGCCGGGC[A/G]TGGTGGCTCACACCT | 284434 |
rs148707101 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NWD1 | GRCh38.p7 | 19:16774299 | CCTTCCATTTATCCA[C/T]CAATTCATCTATCAA | 284434 |
rs148765608 | snp | A/G | 0.000167266 | 0.00914358 | missense | NWD1 | GRCh38.p7 | 19:16773263 | GTGCTGGTGCCCCTC[A/G]GAGGATTCCTCCAGC | 284434 |
rs148770503 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | NWD1 | GRCh38.p7 | 19:16728817 | GGCGTGGTGGCGGGC[A/G]CCTGTAGCCCCAGCT | 284434 |
rs148773230 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NWD1 | GRCh38.p7 | 19:16784679 | CTCACGCCTGTAATC[C/T]CAGCACTTTGGGAGG | 284434 |
rs148810266 | snp | A/C/G | 0.000154754 | 0.00879531 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815353 | AAATAAAAAAACCCT[A/C/G]TGGGGGTATGGGGCT | 284434 |
rs148829180 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | NWD1 | GRCh38.p7 | 19:16758965 | GCCGAGATTGCACCA[C/T]TGCACTCCAACCTGG | 284434 |
rs148848880 | snp | A/C/G/T | 0.00016685 | 0.00913239 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749585 | CAGACCTTCTGCGGA[A/C/G/T]GCCAGGAACTCCTGG | 284434 |
rs148860195 | snp | A/G | 0.00676609 | 0.0577691 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16719254 | AATTCTTGTGCCTCA[A/G]CCTCCCAAGTAGCTG | 284434 |
rs148870608 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16727204 | AGCACTGGGAAACCA[C/T]AGTTGCTATGGTGAC | 284434 |
rs148881171 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | NWD1 | GRCh38.p7 | 19:16755230 | CTCTCTCTTTTTTGG[C/G]GGGGGACAGGGTCTC | 284434 |
rs148883512 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16813181 | GGATGGAGTTTGGGT[A/G]TCTGAGTTGGTTGTG | 284434 |
rs148902093 | snp | A/G/T | 0.000184518 | 0.00960359 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750193 | GAGGACGCTGAGCCC[A/G/T]GTGCACACAGATTTG | 284434 |
rs148917048 | snp | A/G | 1.65075e-05 | 0.00287289 | missense | NWD1 | GRCh38.p7 | 19:16789152 | AACCTTCATGTGGAT[A/G]AGGCACACAAAGTTG | 284434 |
rs148976229 | snp | G/T | 0.0452528 | 0.143452 | intron-variant | NWD1 | GRCh38.p7 | 19:16744316 | CAGGAGGTTGAGGCT[G/T]CAGTGAGCCATGGTT | 284434 |
rs148997408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16796654 | CCTCTTCTTCCTTCC[C/T]TCTTCCCCTTCTCAT | 284434 |
rs149004219 | in-del | -/ATCATCATC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787905 | ATAATAATAATAATA[-/ATCATCATC]ATCATCATCATCATC | 284434 |
rs149016205 | snp | C/T | 8.23703e-05 | 0.00641704 | utr-variant-3-prime, stop-gained | NWD1 | GRCh38.p7 | 19:16815126 | CATGGTTATCTGATC[C/T]GAGAGAATTTCCAGT | 284434 |
rs149037906 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NWD1 | GRCh38.p7 | 19:16733002 | CAAGGCAGGAGGATT[A/G]CTGGAGGCCAGGAGT | 284434 |
rs149038284 | in-del | -/CT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764693 | ATTCTTTCTATCTCC[-/CT]CTCTCTCTCTCTCTA | 284434 |
rs149064153 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807918 | TCCAGCGTGGCCATT[C/T]TGACGGACTACCGCG | 284434 |
rs149071255 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16742693 | TATATATTTTGAGAC[A/G]GAGTTTCGCTCTTGT | 284434 |
rs149133207 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | NWD1 | GRCh38.p7 | 19:16724211 | AGAGCTCACTAATGC[C/T]GGGCATTTTATAGAC | 284434 |
rs149134976 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16776484 | GAGGCAGGAGAATTG[C/T]TTGAAACTGGAAGGC | 284434 |
rs149137114 | snp | A/G/T | 0.000230863 | 0.0107416 | missense, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800067 | CACCATTTCTGGACC[A/G/T]CACCGGCCTCACCGC | 284434 |
rs149207154 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | NWD1 | GRCh38.p7 | 19:16767100 | GAGGTTTAATTGACT[C/T]ATAGTTCTGCATGGC | 284434 |
rs149243331 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16747615 | TGAGCTCAAGTGATC[A/G]TCCAGCCTCTGCCTC | 284434 |
rs149294917 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | NWD1 | GRCh38.p7 | 19:16745358 | AGCCAAACCATATCA[C/G]GGGGAGCAATGCAGG | 284434 |
rs149297280 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NWD1 | GRCh38.p7 | 19:16804040 | CCTGTTTTAATTCAG[A/G]TTACCTAGAAGCTGA | 284434 |
rs149356325 | in-del | -/T | 0.0869089 | 0.189476 | intron-variant | NWD1 | GRCh38.p7 | 19:16746190 | AAAACCTCACCTTTA[-/T]TTAAAAAAAAAAAAT | 284434 |
rs149360296 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NWD1 | GRCh38.p7 | 19:16791945 | TCTCAAACTCCCAAC[C/T]TCAGATGATCTGCCC | 284434 |
rs149364922 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16743564 | TCCAGGCTATAAGGG[C/T]GGTCAACTTCACCTC | 284434 |
rs149392414 | snp | A/G | 1.79361e-05 | 0.00299462 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807626 | CTCCAGTGAGATCAG[A/G]TGTCTGGAGGTTGCT | 284434 |
rs149453346 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | NWD1 | GRCh38.p7 | 19:16725577 | TTTATTTTTGAGATG[A/G]AGTCTCCCTCTGTCA | 284434 |
rs149454937 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16735821 | GAAGGAAGGAAGGAA[A/G]GAAGGAAAGAAGGAA | 284434 |
rs149456131 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | NWD1 | GRCh38.p7 | 19:16779764 | GCCTCAGCCTCCTGA[A/G]TAGCTGGGACTACAA | 284434 |
rs149482929 | in-del | -/ATCC | 0.301615 | 0.244614 | intron-variant | NWD1 | GRCh38.p7 | 19:16754027 | CTCTATCTTCCATCT[-/ATCC]ATCCATCCATCCATC | 284434 |
rs149570312 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | NWD1 | GRCh38.p7 | 19:16760716 | CTGCCTTAGCTTCCT[C/G]AGTAGCTAGGTTTAC | 284434 |
rs149576715 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16720190 | ACTGAGCACCTACTA[A/T]GTGCCAGGCACGCCA | 284434 |
rs149579762 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16795064 | TGGGATTACACAGGC[A/G]TGAGCCATTGCGCCC | 284434 |
rs149592897 | snp | C/T | 0.00323155 | 0.0400666 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749285 | CGGCTCGCGGATGGC[C/T]GCCTGGACGCTGATG | 284434 |
rs149612847 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | NWD1 | GRCh38.p7 | 19:16728220 | CAGAAAATACAAATC[A/G]GATTTAAAAAAATTT | 284434 |
rs149616726 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16735866 | AAGGAAGGAAGGAAG[A/G]AGGAAGGAAGGAAGG | 284434 |
rs149621232 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | NWD1 | GRCh38.p7 | 19:16756862 | ACCACCCGAGCTCCC[C/G]CTCTTGTCAGGTCAG | 284434 |
rs149624192 | snp | C/T | 5.17996e-05 | 0.00508892 | intron-variant | NWD1 | GRCh38.p7 | 19:16814983 | GTAGGATTGGACCTC[C/T]ACACCCCATTTTTCT | 284434 |
rs149693056 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16775977 | CAGCCAGGGAAATGT[A/G]GTCTTTGTGCGGATA | 284434 |
rs149694092 | snp | C/T | 0.000582038 | 0.0170493 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749559 | ACCTTTGGCAGAGCT[C/T]GGAGGTCATTCAGAC | 284434 |
rs149730535 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | NWD1 | GRCh38.p7 | 19:16789855 | CCTGAATAGCTGGGA[C/T]TACAGGCGCACGCCA | 284434 |
rs149734727 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16741953 | CAGTCTCTACTAAAA[A/G]TACAAAAATTAGCCG | 284434 |
rs149737863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16798192 | ATTTAAGTTCAAAGT[C/T]GTCCAAGCTGGAGAG | 284434 |
rs149771893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16726326 | GTGTTGCCCTGGCTG[A/G]CCTTGAACTGCTGGC | 284434 |
rs149779141 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16734049 | CAGGGTCAGCTTTGC[C/T]TACCTGAACTGAGCT | 284434 |
rs149852918 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NWD1 | GRCh38.p7 | 19:16781182 | CTGAAGAGAGATAGA[C/T]GAGGGTCGGGACTAG | 284434 |
rs149893626 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | NWD1 | GRCh38.p7 | 19:16721864 | GCCTCTAATCCCAGC[A/C]CTTTGGGAGGCTGAG | 284434 |
rs149897388 | snp | C/G | 0.000297693 | 0.0121966 | missense | NWD1 | GRCh38.p7 | 19:16773198 | ATCCAGCACTGGTGG[C/G]ACAGCTATGCCAACA | 284434 |
rs149898770 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NWD1 | GRCh38.p7 | 19:16795845 | CCACTGCTTCTATTG[C/T]GTGGAGCAGCTTCCC | 284434 |
rs149930162 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | NWD1 | GRCh38.p7 | 19:16730045 | AAACTATTTATGGGC[C/T]GGGCGCAGTGGCTCA | 284434 |
rs149939113 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16737350 | CTCACTACAGCCTTG[A/G]ACTCCTGGGCTTCTG | 284434 |
rs149940356 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | NWD1 | GRCh38.p7 | 19:16758510 | CTTGAGCTCTGGCCT[C/T]GAGCAGTCCTCCTGC | 284434 |
rs149942222 | snp | C/G/T | 0.000182793 | 0.00955872 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807737 | ATGCATTCCCCCTCC[C/G/T]GAGGCCCGGAAAGCA | 284434 |
rs149943428 | snp | G/T | 0.0189856 | 0.0955633 | downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16818231 | GCCCAGGAGATCAAG[G/T]CTGTAGTTAGCTATG | 284434 |
rs149947650 | snp | C/T | 0.000280535 | 0.0118401 | missense | NWD1 | GRCh38.p7 | 19:16763835 | TCTGCCAGGTGGCCC[C/T]GCAGCCTCTGTGGTT | 284434 |
rs150010420 | snp | C/T | 1.65614e-05 | 0.00287757 | missense, synonymous-codon | NWD1 | GRCh38.p7 | 19:16815032 | CACCCTTACAGGCAC[C/T]CTGCTGACAGTCCAG | 284434 |
rs150053211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16723975 | TCCTGGGATTACAGG[C/T]GTGAGCCATCTCGCC | 284434 |
rs150097438 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NWD1 | GRCh38.p7 | 19:16735501 | ACAGAGCAAGACTCT[A/G]TCCCCCTGACCAAAA | 284434 |
rs150160530 | snp | A/C | 0.021333 | 0.101051 | intron-variant | NWD1 | GRCh38.p7 | 19:16747279 | TGACCTCTTGATCGG[A/C]CCGCCTTGGCCTCCC | 284434 |
rs150212331 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16722325 | AGACGGTCTTGCTCT[A/G]TCACCCAGGATGGAG | 284434 |
rs150223343 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | NWD1 | GRCh38.p7 | 19:16806646 | AGCCTGAGAGGTTGA[A/G]GCTGCAGTGAGCCAT | 284434 |
rs150255378 | snp | A/C | 0.126909 | 0.217598 | intron-variant | NWD1 | GRCh38.p7 | 19:16738860 | TATATAATACATTAT[A/C]TATAATATATAATAC | 284434 |
rs150265309 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16770363 | CTCCTCCCGCCTTGT[A/G]AAGAAGGGCGTGTTT | 284434 |
rs150347244 | snp | A/G | 1.73619e-05 | 0.00294629 | synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749731 | GCCAAGGCTGCTGGG[A/G]CACAAGACAGTGACC | 284434 |
rs150368466 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | NWD1 | GRCh38.p7 | 19:16725386 | GGGAGGCTGAGATGG[A/G]AGGATCACTTGAGCC | 284434 |
rs150379147 | snp | A/G | 0.00105953 | 0.0229923 | missense | NWD1 | GRCh38.p7 | 19:16750396 | CCCACGTGCTGGGCT[A/G]CATTGTGTCTTCCCG | 284434 |
rs150409927 | snp | A/G/T | 9.93291e-05 | 0.00704674 | missense, utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16799962 | TGAGCCTGCTGGCCC[A/G/T]CGGCGGGGCTTTGGT | 284434 |
rs150443455 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16791167 | TGAGCCCAGGAGGTC[A/G]ATGCTGCAGTGAGCC | 284434 |
rs150449559 | in-del | -/A | 0.0444908 | 0.142359 | intron-variant | NWD1 | GRCh38.p7 | 19:16732903 | CTGCTTATGAGAATG[-/A]TTCATTGCACCAAAG | 284434 |
rs150477676 | snp | A/G/T | 0.00529695 | 0.0511913 | missense, utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16799964 | AGCCTGCTGGCCCGC[A/G/T]GCGGGGCTTTGGTGG | 284434 |
rs150530250 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | NWD1 | GRCh38.p7 | 19:16723730 | TTTGAGATGGACTGT[C/T]CCTCTGTTGCCAAGG | 284434 |
rs150533042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16775842 | CTGGCTAATTTTTGT[A/G]TTCTTGGTAGAGACA | 284434 |
rs150537884 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | NWD1 | GRCh38.p7 | 19:16730896 | TATTGCGATTTTTTT[A/T]ATTTTTCTTTCTTTC | 284434 |
rs150543423 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | NWD1 | GRCh38.p7 | 19:16808645 | GACAGGGACCCCACT[A/G]TCACGAGGCTGTAGT | 284434 |
rs150565947 | snp | A/G/T | 0.000165518 | 0.00909578 | missense, stop-gained | NWD1 | GRCh38.p7 | 19:16808122 | CGCAAGTGGAAATTC[A/G/T]AGATGAGCTACACGG | 284434 |
rs150575186 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16741301 | GCTGCTCCCCCTGCC[G/T]GCAAGATACTCTGCC | 284434 |
rs150585037 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16772264 | CAGCTAATATAGAGG[C/T]TGTGGCCGGAAGATC | 284434 |
rs150696874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16733645 | GGAAATTCCACTCTG[C/T]CCACCATTGATCATG | 284434 |
rs150698122 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NWD1 | GRCh38.p7 | 19:16752951 | TGCAGTGAGCTGTGA[C/T]CATGCCACTGCACTC | 284434 |
rs150700806 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16812378 | TTGGAATCAAGATCA[C/T]ATTGTCTGGGTCAGG | 284434 |
rs150730403 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | NWD1 | GRCh38.p7 | 19:16721094 | GCCTCAAGTAATCTG[C/G]CTGTTTTGGCCTCTC | 284434 |
rs150732054 | snp | C/G/T | 0.000163441 | 0.0090386 | synonymous-codon, intron-variant | NWD1 | GRCh38.p7 | 19:16794546 | AGATGAGTCCCTCCT[C/G/T]GCCGCAGGTAGCGTT | 284434 |
rs150741756 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | NWD1 | GRCh38.p7 | 19:16746154 | GAGCCCCGAGTTGGA[G/T]ACCAGTCTGGGCAAC | 284434 |
rs150743080 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | NWD1 | GRCh38.p7 | 19:16804981 | AGGTGCACCACCATG[C/T]CTGACTCCTGGAGAC | 284434 |
rs150759890 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | NWD1 | GRCh38.p7 | 19:16767771 | GAGATTTGGGTAGGG[A/T]CACAGAGCCAACCCA | 284434 |
rs150784065 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718562 | CTCTGTCGCCCAGGC[A/T]GGAGTGCAGTGGCGC | 284434 |
rs150795937 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16801878 | ACTCTGTTAGTTCTC[C/G]CGAGGTTGTTAAAAA | 284434 |
rs150877756 | snp | A/G | 0.00289942 | 0.0379645 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749939 | AACTTCGAGTCTCTC[A/G]TGCTCCTGCTGGATG | 284434 |
rs150921105 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | NWD1 | GRCh38.p7 | 19:16765966 | AGGTTACAGTGAGCC[A/G]AGATCGCACCACTGC | 284434 |
rs151016489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16735163 | CTCTGTGTCTCCTAA[C/T]GTTTTACCTAACCAC | 284434 |
rs151020768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16813479 | AGCCTGTTTTTGTTT[C/T]TTGTTTTTTGTTTTT | 284434 |
rs151069347 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16757841 | CAGATCACCTGAGAT[C/G]AGGAGTTGAACAGCA | 284434 |
rs151080270 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NWD1 | GRCh38.p7 | 19:16770144 | CACATTGATATGGTT[C/T]GGCTGTGTCCCCACC | 284434 |
rs151090114 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | NWD1 | GRCh38.p7 | 19:16803105 | GTGGCAGGCAAGAGA[A/G]TGTGTGCAGGGGAAT | 284434 |
rs151112847 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | NWD1 | GRCh38.p7 | 19:16726081 | GATTCTCCTGCCTCA[A/G]CCTCCGGAGTAGCTA | 284434 |
rs151133930 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | NWD1 | GRCh38.p7 | 19:16795573 | AGGCACCTGCTACCA[C/T]GTCCCGCTAATTTTT | 284434 |
rs151137165 | snp | C/G | 1.73516e-05 | 0.00294542 | missense | NWD1 | GRCh38.p7 | 19:16762132 | ACCACTGAACTTGGA[C/G]CGAAAGGTGAGGTAC | 284434 |
rs151185118 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NWD1 | GRCh38.p7 | 19:16792360 | CAGCCTGGCCAACAT[A/G]GCAAAACCCTGTCTT | 284434 |
rs151264009 | snp | C/G | 0.000182474 | 0.00955007 | missense, utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16799950 | TCGGGGCCCCCGTGA[C/G]CCTGCTGGCCCGCGG | 284434 |
rs151282173 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16789376 | GATTAGACAATCCTG[A/C]TAATTCTTTCTGACC | 284434 |
rs151289059 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | NWD1 | GRCh38.p7 | 19:16742731 | GCTGGAGTGCAATGG[C/T]GCAATCTCGGCTCAC | 284434 |
rs151323679 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748272 | TACAGGCATGAGACC[C/T]CATGTCCAGCCCGTT | 284434 |
rs180714698 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751723 | GGAGAATCACTTGAA[C/T]CCGGGAGGCAGAGGT | 284434 |
rs180742865 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16813689 | ACCATGTTGGCCAGG[A/C]TGGTCTTGAACTCCT | 284434 |
rs180770247 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16776533 | AGATCGTTCCACTGC[A/C]CTCCAGCCTGGGCGA | 284434 |
rs180777938 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16738527 | TGAGCCGAGATTGTG[A/C]CACTGCATTCCAGAC | 284434 |
rs180780072 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16796073 | AGTGTGGCTGAGTCT[A/G]GGCGTTTTTATAGGC | 284434 |
rs180795169 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16728010 | AGGTTGCAGTGAGCC[A/C]AGATCGCGCCATAGC | 284434 |
rs180807053 | snp | A/C/T | 0.00398564 | 0.0444627 | intron-variant | NWD1 | GRCh38.p7 | 19:16755156 | AATCAATCAATAAAT[A/C/T]TCTATATCTATCTCT | 284434 |
rs180810703 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16719720 | AACTGCACCTCCTAG[A/C]CTGTCAGCAAATGGC | 284434 |
rs180840838 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16791675 | CAGCTTGAAAGTGCT[C/T]AGATGTGCTAGAAGT | 284434 |
rs180852490 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16771438 | TTGCACGACAGAGCA[A/G]GACTCTGTCTCAAAA | 284434 |
rs180860044 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16808274 | GAGGCACTTGGTCAG[G/T]CGCAGTGGCTCACGC | 284434 |
rs180867312 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NWD1 | GRCh38.p7 | 19:16750993 | TTGGGAGGCCGAGGC[A/G]GGCGGATCACCCAAG | 284434 |
rs180884542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16734252 | GCCAAGTTCCTTTTT[C/T]AAAAAAGCTTTTCTG | 284434 |
rs180897002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16759074 | TGCCCTAACCGTGCT[C/T]GGTACCTTGTGGGCG | 284434 |
rs180941275 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16722477 | TATTTTTAGTAGAGG[C/T]GGGGTTTCTCCATGT | 284434 |
rs180954297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16781614 | CAGCGAGACCCTATC[C/T]CAAAAAAAAAAGCAA | 284434 |
rs181327136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16775987 | AATGTGGTCTTTGTG[C/T]GGATAACTATGTACT | 284434 |
rs181328346 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16813177 | GTATGGATGGAGTTT[C/G]GGTGTCTGAGTTGGT | 284434 |
rs181345454 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NWD1 | GRCh38.p7 | 19:16754147 | ACCTTTCATCCATCC[A/G]TCCATCATCTCTATC | 284434 |
rs181357591 | snp | C/T | 0.0162398 | 0.0886349 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718893 | GCAGTGGTGCGATCT[C/T]GGCTCACTGCAAGCT | 284434 |
rs181357795 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16738051 | CTATAGCCTGAAAGG[A/C]AAGTGTGGCCTGCTG | 284434 |
rs181408905 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16737836 | TGGGCATGGTGGCAC[A/G]TGCCTGTAATCCCAG | 284434 |
rs181414314 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16787889 | AACAATAATAATAAT[A/G]ATAATAATAATAATA | 284434 |
rs181438461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16746835 | TGCTGTTGATTAAAC[A/G]TAAGTGGATCATCAG | 284434 |
rs181491248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16801195 | GAGGCAGAAGAATAG[C/T]TTGAACCTGGGAGGC | 284434 |
rs181509195 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16783753 | TAAACAAATAAATAC[A/G]ATTTTTACAAAGGAA | 284434 |
rs181519606 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16760317 | GGCTGCAGTACAGTG[G/T]TTGTCATCATGGCTC | 284434 |
rs181524307 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16806572 | AAAAATTAGCTGGGC[G/T]TGGTGGCCCGAGCCT | 284434 |
rs181555941 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16733130 | GGAGGCTGAGGTGGG[A/C]GGATCACTTGAACCC | 284434 |
rs181562420 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16764047 | AACATGGAAATCCTT[C/G]GTTCCTCCTAAGGCA | 284434 |
rs181567599 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16743449 | CTGGGCTCAAGAGAT[A/C]CTCCTGCCTTGGCCT | 284434 |
rs181572232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16729800 | CTTGAATCTGGTAGG[C/T]GGAGGTTGCAGTGAG | 284434 |
rs181606361 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16805413 | TGCCCAGGGTGGTCT[A/T]GACCTCCTGGGCTCA | 284434 |
rs181612059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16755608 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGGCCTCA | 284434 |
rs181618831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16763641 | ACCTCTGGCTTTGAT[C/T]CTCTGAGTCCCAGAT | 284434 |
rs181621417 | snp | C/T | 0.000132771 | 0.00814666 | missense | NWD1 | GRCh38.p7 | 19:16808135 | TCGAGATGAGCTACA[C/T]GGTGGGTGGCCCGCC | 284434 |
rs181626777 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16738855 | TATTATATATAATAC[A/G]TTATCTATAATATAT | 284434 |
rs181631279 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787446 | TTCAACATCTGGGGC[A/G]ACTGATTGACTCCCA | 284434 |
rs181633017 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16720113 | TCAGCTGTCTTCTTC[A/G]GCAACAAACAGAAGT | 284434 |
rs181642592 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16770825 | GAAACCCTATTTTTG[G/T]CATCTGCAAAATGTG | 284434 |
rs181655082 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16733450 | TGCTTGAACCTGGGA[A/G]GTGGTGGTTGCAGTG | 284434 |
rs181694927 | snp | A/G | 6.60786e-05 | 0.0057476 | missense | NWD1 | GRCh38.p7 | 19:16791563 | ACACCTACCTGTGCC[A/G]TCTCAGTCCAGAAGC | 284434 |
rs181708897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16723250 | GTTGTCCAGGCTGGG[A/G]TACAGTGTTGCGATC | 284434 |
rs181734320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16796553 | TGGTTCAAAGGTACA[A/G]TTTCACTGGGGACCC | 284434 |
rs181788165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16729476 | CCTTCTCTGCCCCTC[A/G]ATGTAAAGTAGATTT | 284434 |
rs181963368 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | NWD1 | GRCh38.p7 | 19:16776801 | AAAAAAAAAAGCTGG[A/T]CATGGTGGTATGTGC | 284434 |
rs181991500 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | NWD1 | GRCh38.p7 | 19:16809703 | GGGACTACAGGTGCC[C/T]GCCACCACGCCTGGC | 284434 |
rs182014786 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16746277 | ACGTGGGAGGATTGC[A/G]TCAGCCTAGGAGGCG | 284434 |
rs182043070 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16782526 | TAAAGAGCTGAATCA[A/G]ATTTCTATTAGAGAT | 284434 |
rs182057655 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16759694 | TCAGCCTGGGCAACG[G/T]AGCGAGGCCCCATCT | 284434 |
rs182065510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16722994 | TCACTGGGAGGGGAC[A/G]ACTGAAATCTCACAC | 284434 |
rs182082026 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16743128 | GGCCAGACTGGTCTC[A/G]AACTCCTCTTGACCT | 284434 |
rs182087681 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16788261 | ATAATAATAATAATA[A/T]TAATAATAATAATAA | 284434 |
rs182103096 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NWD1 | GRCh38.p7 | 19:16806740 | CATAAATAGGCTGGG[C/T]GCGATGGCTCATGCC | 284434 |
rs182104388 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16747243 | GGTTTCCCCATGTTG[C/G]TCAGGCTGGTCTCGA | 284434 |
rs182109846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16764524 | GTCCATCCATCCATC[C/T]ATCATTCTATCTATC | 284434 |
rs182112746 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16730194 | AGGTGTGGTGGTGCA[C/T]GCCTGTAATCCCAGC | 284434 |
rs182271021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16791745 | GGAGATGAAGTTTCA[C/T]TTTTGTTGCCCAGGC | 284434 |
rs182302069 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16736156 | GTCACCTTATTTCTC[A/G]TGACCTTGGCAGTCT | 284434 |
rs182379737 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NWD1 | GRCh38.p7 | 19:16814584 | AATCTGATACATAGT[A/G]AACTATAACACTATT | 284434 |
rs182404670 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816401 | TGACTTCAGGACTCA[C/T]GCTGGCAGTAAAACA | 284434 |
rs182430692 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | NWD1 | GRCh38.p7 | 19:16779092 | GCTAGACTAGACAGA[C/G]ACTTATGACCACACT | 284434 |
rs182435415 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | NWD1 | GRCh38.p7 | 19:16740934 | GAGGCCGAGGCAGGC[A/G]GATCACTTGAGGTCA | 284434 |
rs182540486 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16772425 | AGCACTTTAGGAGGC[C/T]GAGGCAGGTGGATCA | 284434 |
rs182566455 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NWD1 | GRCh38.p7 | 19:16800515 | CGGCCTGGGCGACAG[A/G]GTGAGACTCTGTCCC | 284434 |
rs182576363 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16761289 | TTGCATTGTTTCCAC[A/G]TTTTTGCTGTTGTGA | 284434 |
rs182604558 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16724943 | AGGTGGTCCACCCAC[A/C]TCGACCTCCCAAAGT | 284434 |
rs182631720 | snp | C/G/T | 0.00478364 | 0.0487146 | intron-variant | NWD1 | GRCh38.p7 | 19:16811381 | TTGAGGTCAGGAGTT[C/G/T]GAGACCAGCCTGACC | 284434 |
rs182661461 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16756786 | AGGTGAGCAGTGGGC[A/G]AACAAGTGAAGCTTC | 284434 |
rs182663035 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16774554 | ATCCATCCACCCATC[C/T]GTTATTCATCGATTC | 284434 |
rs182671307 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16793452 | ACTATGTTGCCTAGG[C/G]TGGTTTCAAACTTAT | 284434 |
rs182673410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16752590 | AGACTGCAGTAAGCC[A/G]TAATTGTGCCACTGG | 284434 |
rs182702757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16720891 | AGCCTTGCTCTGTTG[C/T]CCAGGCTGGAGCGCA | 284434 |
rs182747641 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16803404 | GGAATTTGGTGGGGG[G/T]GTGGGGACACAAATC | 284434 |
rs182764576 | snp | C/T | 0.00874735 | 0.0655527 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815636 | ACTGGTCCCAATTGG[C/T]CCATACGCCTAGCCC | 284434 |
rs182775852 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16797290 | TTCCCCGTCCTGGAT[C/G]CCTTCTCCTGGCACC | 284434 |
rs182793080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16778349 | TGTTTGCCCAATTCA[C/T]TGGCAAATATATATT | 284434 |
rs182803968 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16756425 | AGAGACAGCACAGGC[A/G]GAAGAAAATCCACAT | 284434 |
rs182814218 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16739486 | AGAGAACCTAGGGGT[A/G]ATCTCTGAGCTTCTC | 284434 |
rs182861750 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16784539 | CCCAGGCACAGGGAG[C/T]AGCAAGTGCAAAGGC | 284434 |
rs182873844 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16744156 | CACTTTGTGAGGCTG[A/C]GATGAGAGGATCCCT | 284434 |
rs182916469 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16751540 | GCATGGTGGCTTACG[C/T]TTTTAATCGCAGCAC | 284434 |
rs182925499 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16735481 | ACTAAGCTCCAGCCT[G/T]GGTGACAGAGCAAGA | 284434 |
rs182977249 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16801946 | AGATTGCTTGAGGCC[A/G]GGAGTTCAAGACCAG | 284434 |
rs183125615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16788804 | TCCTTTATAGCCTGT[C/T]TGCCAGGGTTTTCTT | 284434 |
rs183136065 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748483 | TACAGTGTGACTGCT[C/T]CTCACATGGGACCTC | 284434 |
rs183156919 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16720380 | GATGGTCAGAGACAG[A/C]CTCTCAGGAGGAGGT | 284434 |
rs183214806 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16788327 | GTAATCCCAGCACTT[C/G]GGAGGCTCAGGTGGG | 284434 |
rs183228455 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | NWD1 | GRCh38.p7 | 19:16807325 | ATGGAGAAACCCCAC[A/C]TTTACTAAAAATACA | 284434 |
rs183257217 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16810454 | AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAAAGA | 284434 |
rs183308399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16773544 | TCTTCTAATGAGCCC[A/G]ATGCTAGGGGGTGCC | 284434 |
rs183341663 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16780347 | TTTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT | 284434 |
rs183382303 | snp | C/T | 1.81681e-05 | 0.00301392 | intron-variant | NWD1 | GRCh38.p7 | 19:16807572 | AAGTCATTCTCATTT[C/T]TCTTCCCTGGCAGGC | 284434 |
rs183382648 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16785242 | ATAGGCCAGGCGCGG[C/T]GGCTCACGCATGTAA | 284434 |
rs183385942 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16766580 | ATTATAGCAAAATAC[A/C]TGTCTTAACCATTTT | 284434 |
rs183394088 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16802523 | CTTGCTTCCTCTGGC[C/T]GTATGACCTCTGCAC | 284434 |
rs183411095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16725533 | GAGTTTATTTATTTA[C/T]TTAATTTTATTGTTC | 284434 |
rs183414778 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744827 | CATTTCTTGCAAATG[C/G]CAAACCAGTCAACCT | 284434 |
rs183447127 | snp | C/T | 0.000798403 | 0.0199641 | synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16731242 | GCCTACCCTGAAGTG[C/T]CAGACCTTCTGCCAG | 284434 |
rs183496751 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16762725 | GGACTGGGGAGGCTG[C/G]AGGCAGGACCAGGCT | 284434 |
rs183542651 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16792147 | ATCTCTAAGACATGG[C/T]GTGGAATGAGGTTGA | 284434 |
rs183644965 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NWD1 | GRCh38.p7 | 19:16789757 | GAGTCCTGCTCTGTC[A/G]CCCAGGCTGGAGTAC | 284434 |
rs183646318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748819 | ACAGAGTGAGACCCT[A/G]TCTCAATAATAATAA | 284434 |
rs183651297 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16768333 | GCTAAGAATTTCCTT[C/T]CTTTTAAAGGCTTAA | 284434 |
rs183664510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16731925 | CTTGGGACTATAAAA[A/G]GGCAGGTGGGACTGG | 284434 |
rs183688974 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16747749 | CCCAGCGCAGGCAAC[C/T]ATCAATCTGCTTTCT | 284434 |
rs183859033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16765328 | TGTGAATTTTCCCCC[A/G]GCAGTGCTTCTAGAA | 284434 |
rs183935487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16776437 | GCCGGGCGTTGTAGC[A/G]GACACCTGTAATCCC | 284434 |
rs183935687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16813315 | CAATCTGTTTCCAGG[C/T]GTTTGTGAAGGTTCC | 284434 |
rs183940860 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16795445 | TTTTTGAGACCGAGT[A/C]TCGCTCTATTGCGTA | 284434 |
rs183947291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16754582 | CTCTAAAGTCCATCT[A/G]TCCTTCCATCCATCA | 284434 |
rs184019840 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816663 | CAGTCTTCTCAGGCT[C/T]TTACTTTAATGCTAG | 284434 |
rs184056429 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16751172 | GAGGTTGCCGTGAGC[C/T]GAGATCACGCCATTG | 284434 |
rs184068974 | snp | C/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817666 | AACCTAATAATTTAG[C/G]ATTCTTCTGCCATTT | 284434 |
rs184072686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16781064 | TTGTCGACCTCAGAT[C/T]CTAAGTAAGGTTGTT | 284434 |
rs184078250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16799560 | TGCCCAGGCTTGCGT[A/G]CAATGGCACGATCTT | 284434 |
rs184093981 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16757967 | TGAGGCAGGAGAATC[A/G]CTTGAAGCCAGGAGG | 284434 |
rs184130409 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16782073 | CACTCCAGCCTGGGC[A/G]ACAGAGTGAGACTCT | 284434 |
rs184138128 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16743039 | TGCCTCAGCCTCCCT[A/G]GTAGCTGGGATTACA | 284434 |
rs184163203 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16727272 | CCCGTGCCTAGAGGA[A/G]CCAACATCCAGAGGT | 284434 |
rs184189691 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16753932 | CTATCCATCATCTCA[A/G]TCCTCCATCCTTCCA | 284434 |
rs184200105 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16775662 | GAAATATGTTTTTAT[A/G]TTTTTATTTTTATTT | 284434 |
rs184216162 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718590 | CGCAATCTCGGCTCA[C/T]TGCAAGCTCCACCTC | 284434 |
rs184222212 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16734852 | CAGCCTCCCATAGTG[C/T]TGGGATTATAGGGGT | 284434 |
rs184268008 | snp | A/G | 0.00138868 | 0.0263137 | intron-variant, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800178 | GTTGGTAAGGTATAA[A/G]TATGGTCATTTTTGT | 284434 |
rs184288341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16722817 | ACCTCTGGAGGGGCT[A/G]GGGATTAAGGTCAGC | 284434 |
rs184530905 | snp | A/C | | | downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16818043 | GTTGGCTGGTCAATG[A/C]TTGTAATCCCAGCAC | 284434 |
rs184671429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16779885 | AAGTGATCCTCCCTC[C/T]TTAGCCTACCAAGTA | 284434 |
rs184687278 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16757227 | GCCAAAAAGACTGGG[A/G]ACTGCTGCCCTACAA | 284434 |
rs184699643 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16721587 | GGGCCTCAGTGAGAT[C/T]AGCAGGCTGCAGCTA | 284434 |
rs184702269 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16741452 | TTCACTGAAACCTCC[C/T]TCTCCTGGGTTCAAG | 284434 |
rs184711502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16804252 | TCAATTCCGGCCACT[A/G]TAACAGAATGCCATG | 284434 |
rs184718134 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16763003 | TGGCCAGGCTGGTCT[C/G/T]GAACTCCTGATCTCA | 284434 |
rs184722231 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16738123 | CCACTTGTTTACACA[C/T]TGTTTAGCCCTGCTT | 284434 |
rs184832335 | snp | A/G | 0.000581207 | 0.0170372 | missense | NWD1 | GRCh38.p7 | 19:16791614 | TTTAGCAATGGCTCC[A/G]TCTCTTTGGTAAGCA | 284434 |
rs184839069 | snp | A/G | 9.88354e-05 | 0.00702908 | missense | NWD1 | GRCh38.p7 | 19:16807952 | TCTACAGCATGACCA[A/G]TGGGGACCTCTTTCT | 284434 |
rs184858353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16786260 | TGACCCTCCCACTTC[A/G]GCCCCTGAAAGTGCT | 284434 |
rs184867465 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NWD1 | GRCh38.p7 | 19:16746043 | CCCCAAAACGTAACT[A/G]CTAATAGCCCACCAA | 284434 |
rs184882681 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16750997 | GAGGCCGAGGCGGGC[A/G]GATCACCCAAGGTTG | 284434 |
rs184891087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16722373 | AGCTCACTGCAATGT[C/T]CGTTTCCTGGGTTCA | 284434 |
rs184905554 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16734274 | GCTTTTCTGTCAGGG[C/T]GAGGTGGCTCATGCC | 284434 |
rs184957341 | snp | G/T | 0.000116193 | 0.00762123 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16808136 | CGAGATGAGCTACAC[G/T]GTGGGTGGCCCGCCT | 284434 |
rs184972578 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NWD1 | GRCh38.p7 | 19:16805120 | CTGGAGTGCAGTGGC[A/G]TGATCTCAGTTCACT | 284434 |
rs184986554 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16742815 | AGCTGGGACTACAGG[C/T]ATGTGCCACCATGCC | 284434 |
rs184991355 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16812572 | TACTTGGGAGGCTGA[A/G]GCAGGAGAATCGCTT | 284434 |
rs185001343 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16746100 | TGGCTCATGCCTGTA[A/G]TCCCAGCACTTTGGG | 284434 |
rs185005099 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16786736 | ATTTTTAGTAGAGAC[A/G]GGGTTTTGCCTTGTT | 284434 |
rs185009076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16763355 | CCTGACCTACCCAGC[C/T]TGATATTCAGTGCCT | 284434 |
rs185013795 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16728632 | ATTACATCCTGGTTC[A/G]GGGAATGGACACATA | 284434 |
rs185029736 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | NWD1 | GRCh38.p7 | 19:16745564 | TGACACCTCATCTCT[A/C]CAAAAAAAAAAAAAA | 284434 |
rs185087485 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16795024 | TGACCTCAGGTGATT[C/T]GCCCACCTTAGCCTC | 284434 |
rs185154799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16726848 | ATCCCTGGTCTCCAC[C/T]CACGTGATGCCAGTA | 284434 |
rs185246800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16791693 | ATGTGCTAGAAGTTG[A/G]GAAAAATAATCTTGC | 284434 |
rs185259205 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16772004 | ATAGAACGGTTTTAG[G/T]TTCACAGCAAAATTG | 284434 |
rs185261256 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | NWD1 | GRCh38.p7 | 19:16808613 | AGTTTTTTTTGTTTT[A/C]ATTTTTTTTTTAAAG | 284434 |
rs185414208 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16730063 | GCGCAGTGGCTCACG[C/T]CTGTGATCCCAGCAC | 284434 |
rs185419167 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16746900 | GAGTAGGAAGAGGAG[C/G]GGTTGGTCTTGCTGT | 284434 |
rs185509349 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16798749 | CTCCTGCCTCAGCCT[C/T]GCAAGTAGCTGGGAT | 284434 |
rs185509557 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16769961 | TCTCACCTCAGCCTC[A/C]CAAGTAGCTGGGACC | 284434 |
rs185540547 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16732787 | CTACAGACATGCAGC[A/G]CTATCCCTGGCTAAC | 284434 |
rs185559303 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16733463 | GAGGTGGTGGTTGCA[A/G]TGAGCCGAGATAACG | 284434 |
rs185625143 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16790781 | TGATTACATGTTGAA[A/G]TGATACCACTTGGAC | 284434 |
rs185637677 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16794631 | GTGGGGCTTGGGAAC[A/T]GAGAGAAGTCCTAGG | 284434 |
rs185656975 | snp | A/T | 0.000436467 | 0.0147663 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749097 | GTCAGCTGCTGACCC[A/T]ATAATGACCACACTT | 284434 |
rs185675807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16752989 | GGCAACAGAGCAAGA[C/T]CCTGTCTCCAAAAAC | 284434 |
rs185678285 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16717889 | GTTTTGCTCTGTTGC[C/T]CAGGCTAGAGTGCAG | 284434 |
rs185733291 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16801580 | AATTAGCTCGGTGTA[C/G]TGGCTCACATCTGTA | 284434 |
rs185758848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16784437 | GGCTATATGCAAATA[C/T]GACACTATTTCGTAT | 284434 |
rs185763727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16811768 | TTTTCATTGGATCCA[C/T]CCCCCTGTGGGGCGC | 284434 |
rs185792534 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16775088 | TGTGGTTCAAATGTC[A/G]GAGCTCCTTACTGTG | 284434 |
rs185802910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16737217 | AAATCAATCTCCAGT[C/T]CACAATTAATGGTTT | 284434 |
rs185900663 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16720177 | GTGATGATAATTTAC[C/T]GAGCACCTACTATGT | 284434 |
rs185908504 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | NWD1 | GRCh38.p7 | 19:16738886 | AATACATTATATATT[A/T]TATATATATATATTT | 284434 |
rs186233826 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16799499 | GCACCTGGCCTATTT[A/T]TTTATTTTTATTTTT | 284434 |
rs186236102 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16801983 | CAACATGGACCTTGT[C/T]GCAATAAAAATAAAA | 284434 |
rs186253748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16806644 | AGAGCCTGAGAGGTT[A/G]AGGCTGCAGTGAGCC | 284434 |
rs186263752 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16777225 | GGGGAGGGGAAAGGG[A/G]AGGGGAGGGGAGGGA | 284434 |
rs186264096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16761624 | CGCCTCAGCCTCCCA[A/G]AGTGCTGGGATCACA | 284434 |
rs186267614 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16805776 | GTTTGCCAAATTAAC[A/G]ACTGAATGAAGTTGA | 284434 |
rs186279375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16796988 | GTTTGAGACCAGCTT[A/G]GCCAGCATGGTGAAA | 284434 |
rs186279709 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16756009 | ACATAAATGGTCGAC[A/G]AACATGTATTTCATA | 284434 |
rs186282752 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16764199 | GCTGCTTAATACCCT[A/G]CAGTGCACAGGACAC | 284434 |
rs186284196 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16788270 | ATAATAATAATAATA[A/T]TAATAATAATAATAA | 284434 |
rs186305768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16806907 | CTCTAGTCCCAGCTA[C/T]CCGGGAGACTGAGGT | 284434 |
rs186310431 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16747357 | TCTTTTTATTTATTT[A/G]TTTATTTATTTATTT | 284434 |
rs186327339 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16764731 | CATTCACCAATCCCC[A/G]TGATTCTTAACCAGA | 284434 |
rs186341546 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | NWD1 | GRCh38.p7 | 19:16730353 | AAAAACAAAAAAAAA[A/C]CCCAAAATCTATTTA | 284434 |
rs186382043 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | NWD1 | GRCh38.p7 | 19:16783279 | GTATCAAGCCATCCT[C/G]CCACCTCAGCCTCCT | 284434 |
rs186390762 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16800718 | AGAGAGAGAGAGAAA[G/T]CTCTTGTGTCTCTTC | 284434 |
rs186394148 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16759796 | GTCAGGAGTTTGAGA[C/T]CAGTCTGACCAACAT | 284434 |
rs186402505 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16723089 | GGCAGAGTCTCTCTC[C/T]GTTGCCCAGTGGTGG | 284434 |
rs186407964 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | NWD1 | GRCh38.p7 | 19:16743195 | AGATTACAGGCGTGA[A/G]CCACCTTGCCTGGCC | 284434 |
rs186422613 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787954 | TCATCATAGGCCAGG[C/T]GCGGCGGCTCATGCC | 284434 |
rs186441746 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16760332 | GTTGTCATCATGGCT[C/T]ACTGCAGCCTCAAAC | 284434 |
rs186449826 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16761571 | TTTCACCACGTTGGC[C/T]AGGCTGGTCTTGAAC | 284434 |
rs186458821 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16723261 | TGGGGTACAGTGTTG[C/T]GATCTTGGCTCACTG | 284434 |
rs186466246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16725050 | GGGGTCTCACTCTGT[C/T]GCCCAGGCTGGAGTG | 284434 |
rs186502211 | snp | C/T | 0.00953873 | 0.0683987 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718915 | CTGCAAGCTCCACCT[C/T]CCGGGTTCATGCCAT | 284434 |
rs186547064 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | NWD1 | GRCh38.p7 | 19:16787626 | GCACTTTGGAAGGCC[A/G]AGGCGGGTGGATCAC | 284434 |
rs186548559 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16746399 | TAAACAGTTGGCCGG[G/T]TGCGGTGGCTCATGC | 284434 |
rs186624850 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16743538 | TATTGACCCTCGTGA[C/T]TTCTGGTGGCTCCAG | 284434 |
rs186649501 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | NWD1 | GRCh38.p7 | 19:16771415 | AGATCACGCCACCGC[A/G]CTCCAACTTGCACGA | 284434 |
rs186771431 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16763642 | CCTCTGGCTTTGATT[A/C]TCTGAGTCCCAGATG | 284434 |
rs186775916 | snp | C/G | 0.000115394 | 0.00759499 | missense | NWD1 | GRCh38.p7 | 19:16807816 | TATGACAACATCGTC[C/G]TGGTGCTGGACATCA | 284434 |
rs186809929 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16729549 | GACCAGCCTGAGCAA[C/T]ATGGCGAGGCCCCAT | 284434 |
rs186918316 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16811447 | AAATTAGCCGGGCAT[C/G]GTGGTGCATGCCTGT | 284434 |
rs186940511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16774602 | CCTTTTCATTAATCT[A/G]TCCATCCATCCATTC | 284434 |
rs186949037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16793813 | AACTCCTGACCTCGA[A/G]TGATCCACCCACTTC | 284434 |
rs186955639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16752739 | TGGTGGCTCACACCC[A/G]TAATCCCAGCACTTT | 284434 |
rs187031695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16803471 | GAAAGTAGCTAGTCA[A/G]AAACAGGTTTTCATT | 284434 |
rs187055463 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815966 | TAGTTATAATTTGAT[A/T]CAGGTCACAAGTCCA | 284434 |
rs187060892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16797297 | TCCTGGATCCCTTCT[C/T]CTGGCACCTAGCAGG | 284434 |
rs187065833 | snp | A/G | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748765 | GGAGGCGGAGGTTGC[A/G]GTGAGCTAAGATCGC | 284434 |
rs187069702 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | NWD1 | GRCh38.p7 | 19:16767164 | GAAGGGAAAGAGGTG[C/T]GTCTTTTTTTTTTTT | 284434 |
rs187073745 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | NWD1 | GRCh38.p7 | 19:16731686 | CTCAGCTCACTGCAA[A/C]CTTGGCCTCCAGGGT | 284434 |
rs187076870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16778682 | CCTGGCTAATTTTTA[C/T]ATTTTTAGTAGAGAC | 284434 |
rs187111178 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NWD1 | GRCh38.p7 | 19:16809711 | AGGTGCCCGCCACCA[C/T]GCCTGGCTAATTTTT | 284434 |
rs187115150 | snp | A/T | 6.60862e-05 | 0.00574793 | stop-gained | NWD1 | GRCh38.p7 | 19:16773158 | ACAGAACTGCTGGCC[A/T]GACTCCATTTCTTCG | 284434 |
rs187124768 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | NWD1 | GRCh38.p7 | 19:16734892 | TGCCCTGCCTCTGTT[C/T]TAATTTTTTTATTTT | 284434 |
rs187205813 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16751800 | AGGAAGACTCCATCT[C/G]AAAAAGAAAGAGAAA | 284434 |
rs187222026 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16773555 | GCCCGATGCTAGGGG[A/G]TGCCTCCAAGCTTCC | 284434 |
rs187231926 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16735837 | GAAGGAAAGAAGGAA[A/G]GAAGGAAGGAAGGAA | 284434 |
rs187270533 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | NWD1 | GRCh38.p7 | 19:16755251 | ACAGGGTCTCACTCT[C/G]TTGACCCAGACTGGA | 284434 |
rs187273726 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16796095 | TTTATAGGCACAGGA[C/T]GGGGGAGGGGCAGGT | 284434 |
rs187289165 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16791839 | ACTGCCTCAGCCTTC[C/T]GAGTAGCTGGGATTA | 284434 |
rs187312507 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16719802 | TCTGGGCTGAATGCC[C/T]GGCTAAGCTGGTGCC | 284434 |
rs187328631 | snp | A/G | 0.123105 | 0.215401 | intron-variant | NWD1 | GRCh38.p7 | 19:16751246 | AAAAAAAAAAATGCA[A/G]TAAACTTGGGTCATG | 284434 |
rs187426943 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16814019 | AAAAATTATCCAGGC[A/G]TGGTGGTACATGCTT | 284434 |
rs187491435 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817556 | GCAGTGAGCCGAGAT[C/T]GCACCACTGCACTCC | 284434 |
rs187498339 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16776546 | GCACTCCAGCCTGGG[C/T]GAAAGAGTAAAACTC | 284434 |
rs187508762 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16757507 | GCTTTTGGCAGATGA[A/G]GAAACTGAGGCAAAG | 284434 |
rs187516816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16721836 | TTAACTCTGGCTGCC[C/T]GTGGTGGCTCATGCC | 284434 |
rs187520194 | snp | A/C/G | 0.00438332 | 0.0466095 | intron-variant | NWD1 | GRCh38.p7 | 19:16741968 | ATACAAAAATTAGCC[A/C/G]GGTGTGGTGGTGGGC | 284434 |
rs187633757 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | NWD1 | GRCh38.p7 | 19:16785259 | GCTCACGCATGTAAT[A/C]CTAGCAGTTTGGGAG | 284434 |
rs187645730 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NWD1 | GRCh38.p7 | 19:16802557 | CCAACCCCCTTCACC[C/T]TTTGTATTAAGAAGA | 284434 |
rs187650121 | snp | C/G | | | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744917 | CTGATCAATCTTGGT[C/G]TCAGGATCTTCCTCT | 284434 |
rs187679795 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16762480 | TTTTGTATTTTTAGT[A/G]GAGACGGGGTTTCAC | 284434 |
rs187680883 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16725861 | TCACAGCAGCCTTGA[A/G]CTCTTGGGCTCATGC | 284434 |
rs187778489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16744186 | TTGAGTACAGGAGTT[C/T]AATACCAGCCCGGGT | 284434 |
rs187812748 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16721414 | CAGTAACCAAGGGAG[C/T]GTGGCCAGGCGCTGA | 284434 |
rs187843138 | snp | A/T | | | missense | NWD1 | GRCh38.p7 | 19:16807661 | AGCGCAAGCTCCTAT[A/T]TACGGGCCTCGTGTC | 284434 |
rs187897485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16739846 | TTCCTGGTGGGAACT[A/G]TTCCTATTTCCCTTG | 284434 |
rs187995981 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | NWD1 | GRCh38.p7 | 19:16762917 | GCCTCCCTAGTACCT[C/G]GGACTACAGGTGTGT | 284434 |
rs188023687 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16792404 | AAAATTGACCAGGCA[C/T]GGTGGCTCACACCTG | 284434 |
rs188028769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16726920 | GCAAGTGTCCCCTGG[A/G]GGCTGAATGGTCCCC | 284434 |
rs188048122 | snp | C/T | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16736658 | CTGAGGTGGGGTATT[C/T]GGAACATTGAAGCCA | 284434 |
rs188159141 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16788859 | CTGATGACTTTCACA[A/G]TTCAATTCCATCCAT | 284434 |
rs188188220 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16756727 | CCCATCCCCCAGTAC[C/T]GGTACTGCTCCGTGG | 284434 |
rs188192227 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NWD1 | GRCh38.p7 | 19:16720734 | AATTTTTTGTATTTT[C/T]AGTAGAGACGGGGTT | 284434 |
rs188263487 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16813617 | GAGTAGCTGGGATTA[C/T]GGGCGCCCACCACCA | 284434 |
rs188266162 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | NWD1 | GRCh38.p7 | 19:16785988 | TCCTGCCTCAGCCTC[C/T]CAAGTAGCTGAGATT | 284434 |
rs188269520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16776466 | CCAGCTACTCTGGAG[A/G]CTGAGGCAGGAGAAT | 284434 |
rs188270606 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16810492 | GTAAGTCTAGATTAG[G/T]CACAGCAACTCATGC | 284434 |
rs188273553 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16795519 | CCTCCCGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 284434 |
rs188291105 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | NWD1 | GRCh38.p7 | 19:16745930 | TCTAAATAAATAAAT[A/T]AATTAATTAAATAAA | 284434 |
rs188379479 | snp | C/T | 3.33985e-05 | 0.00408633 | intron-variant | NWD1 | GRCh38.p7 | 19:16791652 | TGACTATGATGTGAA[C/T]ATTAACTCAGCTTGA | 284434 |
rs188383572 | snp | A/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817786 | ATCAAGGGCTTACCC[A/T]ATGCAGAAATAAAGT | 284434 |
rs188411250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16771421 | CGCCACCGCACTCCA[A/G]CTTGCACGACAGAGC | 284434 |
rs188413516 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16734169 | AAACTAAACACCCTC[C/G]TTTGCAAGGAAAGCT | 284434 |
rs188420844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16799582 | CACGATCTTGGCTCA[C/T]TGCAAACTCCACCTC | 284434 |
rs188435673 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NWD1 | GRCh38.p7 | 19:16727649 | CCCAGCGGTGTGACC[A/G]TCTTCATCAGTTCCA | 284434 |
rs188441126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16746068 | CACCAATCACATAAA[C/T]TGTTGACCAGGTGTG | 284434 |
rs188550434 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16788726 | CCTTTGTGCAAGGTT[A/G]TGATTTTTGTAGTTT | 284434 |
rs188551583 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16754010 | TTCCTTTTATCCATC[A/T]TCTCTATCTTCCATC | 284434 |
rs188556791 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16747769 | ATCTGCTTTCTGTCT[C/G]TATTAATTTGCCTGT | 284434 |
rs188569420 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | NWD1 | GRCh38.p7 | 19:16737943 | GTACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 284434 |
rs188577632 | snp | A/C | 0.0162398 | 0.0886349 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718769 | TCCTGACCTCGTGAT[A/C]TGCCTGCCTTGGCCT | 284434 |
rs188649094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16812182 | GTGTGGTGGCACACA[C/T]TTGTAATCCCTGCTA | 284434 |
rs188659876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16775467 | GTAGGGCTGTCCTCG[C/T]TGGCCCAATATAGCT | 284434 |
rs188780792 | snp | C/T | 0.000131963 | 0.00812183 | synonymous-codon, utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16797859 | GAACAACCTGATCAT[C/T]ACGGGGTCCCTTGAT | 284434 |
rs188800950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16756861 | TACCACCCGAGCTCC[C/T]CCTCTTGTCAGGTCA | 284434 |
rs188823266 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16766187 | CTGAGTACAAAACTT[C/T]AGGTTCAGAGTTGGT | 284434 |
rs188825171 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16807388 | ATCCCAGCTACTCGG[C/G]AGGCTGCGGCAGGAG | 284434 |
rs188852090 | snp | A/T | 0.000311915 | 0.0124844 | intron-variant | NWD1 | GRCh38.p7 | 19:16731314 | GCTCCATGCTTTTTT[A/T]ATTTTTTTTTGACAC | 284434 |
rs188912329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16794693 | GCCTCATAGTAAACA[C/T]TTTTTGCAGTCCAGA | 284434 |
rs188915428 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16795155 | GGGGCACCCCATTTA[C/T]TCAGCCTGTGGGGTC | 284434 |
rs188925512 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16775734 | AGTGCAGTGGCGCAA[A/T]CTCGGCTCACTGCAC | 284434 |
rs188931846 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16812954 | TCTGGCCACCTCTAG[C/G]TGCATCCCTTAGCTT | 284434 |
rs188954042 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16753405 | TTTATAAAGCATGAT[A/G]ATAAGGTGGATGATT | 284434 |
rs189074371 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816472 | CCAAACTTTTGGGAT[A/G]AAGATGTGGGTTTTT | 284434 |
rs189090180 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16779550 | CACAGATTCACTTCT[C/G]TGTATTGAAACCCTG | 284434 |
rs189094423 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16741231 | GCCAGTGCCTTAGTC[A/G]CTGTGCCCTTCCTAC | 284434 |
rs189158451 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | NWD1 | GRCh38.p7 | 19:16801067 | CAGATCACTTGAGGT[C/T]GGGAGTTCGAGACCA | 284434 |
rs189164688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16800501 | CTGACTCTGCACTCC[A/G]GCCTGGGCGACAGAG | 284434 |
rs189166544 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16759607 | TGAGGCTGGAAGCAG[G/T]GGCTCATGCCTATAA | 284434 |
rs189174752 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | NWD1 | GRCh38.p7 | 19:16783539 | CTCGGGAGGCTGAGG[A/C]AGGAGAATCACTTGA | 284434 |
rs189301751 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16805386 | TTTTGTAGAGATAAG[G/T]TCTCTCTATCTTGCC | 284434 |
rs189309128 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16754902 | CATCCGTCATATCTA[C/T]CTATCTATGTCTATC | 284434 |
rs189314258 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16719527 | CACTCTCTATATAAA[C/T]GCTTTTCATTGTCTC | 284434 |
rs189320490 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16786314 | GGCCCAGTCATATCC[C/T]TGTTCTGTTATTGTA | 284434 |
rs189331281 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16746180 | GCAACATGGCAAAAC[C/T]TCACCTTTATTTAAA | 284434 |
rs189335012 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16786807 | TCTGCCCGCCTCAGC[C/T]TCCCAACGTGCTGGG | 284434 |
rs189342356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16763419 | ATTTCCCACCCGCAT[C/T]CCCTAACCTGACTTG | 284434 |
rs189353718 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16729021 | CTGCAATCCCAGCAC[A/C]TTGGGAGGCCGAGGT | 284434 |
rs189415064 | snp | A/C | 0.0103295 | 0.0711199 | downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16818106 | CCCAGGAGTTTGAGA[A/C]CCTGTCTCTCCAAAA | 284434 |
rs189416131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16808237 | GGGCCATCGACCAGG[A/G]TGGGACTGGGGTGAT | 284434 |
rs189431622 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782320 | AAGTGTTTTAAATTA[A/G]CCAGGCATGGTGGTG | 284434 |
rs189440871 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NWD1 | GRCh38.p7 | 19:16781363 | GGCGTGGTGGCTTAT[C/T]CCAGCACTTTAGGAG | 284434 |
rs189446629 | snp | A/T | 0.0341408 | 0.126114 | intron-variant | NWD1 | GRCh38.p7 | 19:16742847 | GGCTATTTTTAAAAA[A/T]ATTTTTTGTAGAGAC | 284434 |
rs189466937 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16768569 | TATCTTTTTCTCTAC[C/G]CTTTTATGTTCAGTG | 284434 |
rs189474380 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16743127 | TGGCCAGACTGGTCT[C/G]GAACTCCTCTTGACC | 284434 |
rs189482362 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16790146 | ACACACAATAACTTC[A/G]TGGGTGATAGCTTAC | 284434 |
rs189488453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16722993 | TTCACTGGGAGGGGA[C/T]GACTGAAATCTCACA | 284434 |
rs189579799 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16729627 | TCACACCTGTAATCC[C/T]GGTACTTTAGGGGGC | 284434 |
rs189584348 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | NWD1 | GRCh38.p7 | 19:16738429 | CACAAATTAGCCAGA[C/T]GTGGTGGCACATGCC | 284434 |
rs189593813 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16804775 | CCAGATTTTCTTTGT[C/T]CTCACATGGTAGAAA | 284434 |
rs189600132 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16763114 | TGACCCTTCTCTTCT[C/T]CCCCCGAGACCCATT | 284434 |
rs189666569 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16791696 | TGCTAGAAGTTGGGA[A/C]AAATAATCTTGCCTT | 284434 |
rs189670770 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16761657 | CATGAGCCACTGCAC[C/T]CAGCCTGAACACCTG | 284434 |
rs189682329 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16725066 | GCCCAGGCTGGAGTG[C/T]AGTGGTATGATCTTG | 284434 |
rs189682365 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16772221 | AAATAAAAAACTAAC[A/G]AGGCGTGGTGACGTG | 284434 |
rs189684954 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16809307 | CAGGCTGAACTCCTG[C/G]CCTCAAGTGACCTGC | 284434 |
rs189689886 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744631 | CCAGAGGAGGCCACC[C/T]TAACTTCTGTCCTAC | 284434 |
rs189731891 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16758872 | AATTAGCCAGGCGTG[C/G]TGGCGCCTGTAGTCC | 284434 |
rs189744182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16722443 | TACAGGCATGAACCA[C/T]CACGCCCAGCTAATT | 284434 |
rs189794168 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16787957 | TCATAGGCCAGGCGC[A/G]GCGGCTCATGCCTGT | 284434 |
rs189821180 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16764278 | AACCCCTGCCTTATC[A/C]TGAGAGACCCTATCT | 284434 |
rs189825885 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | NWD1 | GRCh38.p7 | 19:16730138 | ACCATCCTGGCCAAC[A/G]TGATGAAACCCCATC | 284434 |
rs189919149 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816323 | GTTCTGACTTTTAAA[A/G]TTGGCGATTGGTTGA | 284434 |
rs189941139 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16806203 | TATACCTCTATCCTC[C/G]CAGCAGGACTGTGCC | 284434 |
rs189966073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16763710 | GGGTATGTCTGTCTT[C/T]CATTGCATTCTCGTC | 284434 |
rs190046351 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16774284 | CAATCATCTACCCAC[C/T]CTTCCATTTATCCAT | 284434 |
rs190062475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16793326 | GCAGCCTCGACCTCC[C/T]GGGCTCAAGACGTCC | 284434 |
rs190098045 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16791105 | CAGGCATGGTGGTGC[A/G]TGTCTGTGGTCCCAG | 284434 |
rs190135809 | snp | A/G | 8.68259e-05 | 0.00658828 | missense, upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749153 | GTCATTGAGTGGGAG[A/G]TAGAGCGGAGCCTGC | 284434 |
rs190197754 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NWD1 | GRCh38.p7 | 19:16737714 | CGTGGTGGCTCACAC[C/T]TGTAATCCCAGCACT | 284434 |
rs190228564 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16787722 | AAAATTAGCCAGGCG[C/T]GGTGGCACATGCCTG | 284434 |
rs190236691 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NWD1 | GRCh38.p7 | 19:16746576 | TACTCGGGAGGCTGA[A/G]GCAGGAGAATCACTT | 284434 |
rs190275465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16737414 | CTACAGGTGTGTGCC[A/G]CCACAGTTGGCTAGT | 284434 |
rs190339086 | snp | G/T | 6.58935e-05 | 0.00573955 | missense | NWD1 | GRCh38.p7 | 19:16807957 | AGCATGACCAATGGG[G/T]ACCTCTTTCTTTACG | 284434 |
rs190367981 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16770701 | TGCTGGGAAGAGTAC[A/G]CGCATCAGTTCACAC | 284434 |
rs190379036 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732926 | CACCAAAGTCCCATT[A/T]GGTTAAAAGATGAGG | 284434 |
rs190424113 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16732397 | GTTGTTGTTGCTGCT[C/G]TTTTTGTCTTGCCTT | 284434 |
rs190428646 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16811047 | ATTTTTTAATTTTTT[C/G]TAGAGACAGGGTTTC | 284434 |
rs190549338 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718213 | GTAGTGTGGCTCTGT[C/T]GTCCAGGCTGGAGTG | 284434 |
rs190567880 | snp | A/C | 0.00557542 | 0.0525036 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815530 | CAGACTTGCCACCCC[A/C]AGGTTAGCAACATGG | 284434 |
rs190589193 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16778100 | CTCTGTCCCGATGAG[G/T]TGGAAACAAAATTCT | 284434 |
rs190600407 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16797232 | AGGCCCTCCCCCAAC[C/T]AGCTGTGGGCTATGT | 284434 |
rs190606897 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | NWD1 | GRCh38.p7 | 19:16756155 | CTACTTGGGAGGCTG[A/T]GTACGAGAATTGCTT | 284434 |
rs190618252 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | NWD1 | GRCh38.p7 | 19:16720324 | AAAATTAAAATAAGG[C/T]GATGGCATTGGGAGT | 284434 |
rs190618554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16739402 | GGAGACAAAGAACTC[C/T]AGGAGGAATCTGATT | 284434 |
rs190701009 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | NWD1 | GRCh38.p7 | 19:16788272 | AATAATAATAATAAT[A/G]ATAATAATAATAAAA | 284434 |
rs190709494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16764849 | GGTGGGTGGAGGCCA[A/G]GGTTGCTGCTTTACA | 284434 |
rs190717555 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | NWD1 | GRCh38.p7 | 19:16807016 | AGCCAGACTCTGTCT[A/T]AAAAAAACAAAAAAT | 284434 |
rs190727653 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16747538 | CACGCCATCACAGGT[A/G]GCTAACTTATTTTTT | 284434 |
rs190750414 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16743400 | TTTTTATAGATATGG[G/T]GTCTCACTATGTTGC | 284434 |
rs190756300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16759833 | ACCCTGTCTCTATTA[A/G]AAATACAAAAATTAG | 284434 |
rs190760588 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NWD1 | GRCh38.p7 | 19:16723181 | TAGGACCGCAGACAC[A/G]AATCACCATGTCCAG | 284434 |
rs190776531 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16734460 | GAATGGCGTGAACCC[A/G]GGAGGCGGAGCTTGC | 284434 |
rs190838295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16797526 | AGTAGAGAATAAAAT[A/G]CATGAAACATCGGGG | 284434 |
rs190876916 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NWD1 | GRCh38.p7 | 19:16756738 | GTACCGGTACTGCTC[C/T]GTGGCCTGTTAGGAA | 284434 |
rs190889385 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NWD1 | GRCh38.p7 | 19:16720844 | AGGCGTGAGCCACCG[C/T]ACCTGGCCGAGACTT | 284434 |
rs190906410 | snp | A/G | 0.00517822 | 0.0506191 | upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16719936 | TGTCTTCCGGGTGGC[A/G]CCGAGGCCAGGAAAC | 284434 |
rs190971119 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | NWD1 | GRCh38.p7 | 19:16785128 | CAGGGTCTCCTTCTG[C/G]GGGGTTGCGAATGTT | 284434 |
rs191014257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16751042 | GCCTGACAAAACATG[A/G]AGAAACTCTGTCTCC | 284434 |
rs191015616 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16784501 | GCAGGGGTGAAGGAA[A/G]GGCAGGGGAGAGGAA | 284434 |
rs191021782 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16743894 | CACTATGTTGGCCAG[G/T]CCAGTCTTGAACTCC | 284434 |
rs191111513 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16778750 | CTGACCTCAAGTGAT[C/G]CGCCCACCTCGGCCT | 284434 |
rs191122387 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16740706 | CTAACTCCTAAGCTC[A/G]AGTGATCTGCCCACC | 284434 |
rs191126464 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16806662 | GCTGCAGTGAGCCAT[A/G]TTCGTGCCACTGCAC | 284434 |
rs191231685 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16801679 | TGAGATTGTGCCACT[G/T]CACTCCAGCCTGGAC | 284434 |
rs191251042 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16760895 | GTGCCCAGTCAGAAT[C/T]TTAAAGTTGACAATT | 284434 |
rs191286067 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16724535 | GGGCAGGATTCAGGT[C/T]GCCAGGGCATTTTCA | 284434 |
rs191327481 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16811672 | TTCCTTTCAGTGCAA[A/T]ATGTATCTAAACCTT | 284434 |
rs191339575 | snp | A/G | 8.50449e-05 | 0.00652037 | missense, intron-variant | NWD1 | GRCh38.p7 | 19:16794547 | GATGAGTCCCTCCTC[A/G]CCGCAGGTAGCGTTT | 284434 |
rs191347875 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16786552 | CTTTATGTTGGGGAC[A/C]CTTTTTTTTTTTGAG | 284434 |
rs191349669 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16763183 | TCAGCTTCATCCTGC[C/T]TCTCCAGGACATGGT | 284434 |
rs191362966 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16746080 | AAATTGTTGACCAGG[G/T]GTGGTGGCTCATGCC | 284434 |
rs191463357 | snp | A/C/T | 6.66815e-05 | 0.00577382 | synonymous-codon, missense | NWD1 | GRCh38.p7 | 19:16807716 | GAATTCCAGGCAGGA[A/C/T]GTGATATGCATTCCC | 284434 |
rs191489935 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748781 | GTGAGCTAAGATCGC[A/G]CCACTCCACTCCAGC | 284434 |
rs191499194 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16768216 | AGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAT | 284434 |
rs191504100 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16731688 | CAGCTCACTGCAACC[C/T]TGGCCTCCAGGGTTC | 284434 |
rs191629424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16752534 | ATGGTGGTGCTACTC[C/T]GGAGGCTGAGATGGG | 284434 |
rs191642984 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16735841 | GAAAGAAGGAAGGAA[A/G]GAAGGAAGGAAGGAA | 284434 |
rs191687368 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | NWD1 | GRCh38.p7 | 19:16791954 | CCCAACCTCAGATGA[C/T]CTGCCCACCTCGGCC | 284434 |
rs191700312 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751538 | TGGCATGGTGGCTTA[C/T]GCTTTTAATCGCAGC | 284434 |
rs191798860 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NWD1 | GRCh38.p7 | 19:16814276 | GAGGCTGGCAGACTT[A/G]CCTAAGGTCACACAG | 284434 |
rs191836488 | snp | A/T | 0.0678174 | 0.1712 | intron-variant | NWD1 | GRCh38.p7 | 19:16738843 | GTATACATTATATAT[A/T]ATATATAATACATTA | 284434 |
rs191937710 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | NWD1 | GRCh38.p7 | 19:16810302 | AATTAGCCCTGCATG[G/T]TGGTATGTGCCTGTA | 284434 |
rs191976059 | snp | C/G | 0.000481988 | 0.0155165 | missense | NWD1 | GRCh38.p7 | 19:16773244 | CCAGTTGTGCGCACA[C/G]CCTGTGCTGGTGCCC | 284434 |
rs191980766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16735053 | ATAGGCACATGCCAC[C/T]GTGCCCGACTAAATG | 284434 |
rs192001589 | snp | A/C | 0.00557542 | 0.0525036 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817653 | TTAATTTTGCATCAA[A/C]CTAATAATTTAGGAT | 284434 |
rs192013727 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | NWD1 | GRCh38.p7 | 19:16798903 | AGTGCTGGGATTACA[A/G]GCGTGAGCCACCATG | 284434 |
rs192022152 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16757917 | ATTAGCCGGGCGTGG[A/T]GGTGCACACCTGTAG | 284434 |
rs192028850 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16721845 | GCTGCCCGTGGTGGC[A/T]CATGCCTCTAATCCC | 284434 |
rs192038104 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16742700 | TTTGAGACGGAGTTT[C/T]GCTCTTGTTGCCCAG | 284434 |
rs192123482 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16755278 | TGGAGTGCACTGAAG[C/T]GATCACAGCTCGCCG | 284434 |
rs192129262 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16796182 | AGGTGCAGTGGCTCA[C/T]GCCTGTAATTCCAGC | 284434 |
rs192135658 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16730853 | AGGAAACATAAGGAG[A/G]CTCCACAAAATAAAT | 284434 |
rs192151908 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16785657 | ATACATATTTTAATC[A/T]ATATTTTTGTGTATG | 284434 |
rs192167371 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NWD1 | GRCh38.p7 | 19:16803317 | TCAGGTAGTCCTTCA[C/T]AGCAACACCAACAGA | 284434 |
rs192173264 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, missense | NWD1 | GRCh38.p7 | 19:16745072 | ATGGACTCACAATTC[A/C]ACATGGCTGGGGAGG | 284434 |
rs192182742 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718462 | ACAGGCATGAGCCAC[C/T]GCGCCTGACCAAGTA | 284434 |
rs192185777 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16762695 | TGATGTTTCTTTTTC[G/T]CTGTCTTCCCTGCTG | 284434 |
rs192211866 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16805083 | CTTTTGTTTGAGATG[C/G]AGTCTCGCTCTGTCA | 284434 |
rs192248075 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | NWD1 | GRCh38.p7 | 19:16774659 | CCGTCCATCCACCCA[C/T]CCTTCCATCCACTCA | 284434 |
rs192257932 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16737119 | ACAGGGTCTTGGGAT[A/C]TTTTTTTTCCTCCAT | 284434 |
rs192302892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16756876 | CCCTCTTGTCAGGTC[A/G]GCAGCATCATTAGAT | 284434 |
rs192321649 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16741299 | ATGCTGCTCCCCCTG[A/C]CTGCAAGATACTCTG | 284434 |
rs192333017 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16721472 | GGGACCCAGGAAAAC[A/G]AGAGAAGGAACAGAA | 284434 |
rs192368116 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16799596 | ATTGCAAACTCCACC[A/T]CCCGGGTTCAAGCGA | 284434 |
rs192533471 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NWD1 | GRCh38.p7 | 19:16746036 | TTGACTCCCCCAAAA[C/T]GTAACTACTAATAGC | 284434 |
rs192688932 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16790469 | TTGAAATTCGGGGGG[C/T]AGGGGGTAAGGGGAG | 284434 |
rs192718949 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16818032 | AAAGTTTGACAGTTG[G/T]CTGGTCAATGCTTGT | 284434 |
rs192792193 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16786027 | CTGCCACCACACCCA[A/G]CTAATTTTTGTATTT | 284434 |
rs192824438 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | NWD1 | GRCh38.p7 | 19:16727112 | CTGCACACCTGGGCT[C/T]AGGCTCAACTTACAC | 284434 |
rs192872551 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16807395 | CTACTCGGGAGGCTG[C/T]GGCAGGAGGATTGCT | 284434 |
rs192874711 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16766361 | AAACTGTGATTGCTC[C/T]GCTGCATTCCAGCCT | 284434 |
rs192879909 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NWD1 | GRCh38.p7 | 19:16731367 | GCTGGAGTGCAGTGG[C/T]GCGATCTCGGCTCAC | 284434 |
rs192918399 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16794857 | CTCAATCATAATTCA[A/T]TGCAGCCTTGAATTT | 284434 |
rs192928986 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16753571 | CGCCCCCCATCCCCC[A/C]ACAGGGGACACTAGA | 284434 |
rs192947394 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | NWD1 | GRCh38.p7 | 19:16726691 | TGATCCACCCACCTC[C/G]GCCTCCCAAAGTGCT | 284434 |
rs193007136 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | NWD1 | GRCh38.p7 | 19:16803637 | ACTAGCTAGTCATGG[C/G]CAGGTGTGGTGGCTC | 284434 |
rs193007865 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NWD1 | GRCh38.p7 | 19:16762957 | CCTGGCTAATTTTTG[C/T]ATTTTTAGTAGAGAC | 284434 |
rs193083487 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16788764 | TATTAGGCATACAAG[A/C/T]GTGAGAACTCTTTCT | 284434 |
rs193089999 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748176 | TTTAGTAGTGACAAG[A/G/T]TTTCACCATGTTGGC | 284434 |
rs193149632 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16779835 | GAAATGGGGTCTTGC[C/T]ATGTTGCCCAGGCTG | 284434 |
rs193151590 | snp | C/T | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816600 | ACTGTTTTCATTCCA[C/T]TTAAGTGGATCTTTC | 284434 |
rs193169564 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16775640 | CTCCAACTGTAAGGA[A/G]GCCTGGGAAATATGT | 284434 |
rs193206073 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732713 | TCTCACAGCTCACTG[C/T]AACCTTGAGCTTCTG | 284434 |
rs193297791 | snp | C/G/T | 0.00637319 | 0.05614 | intron-variant | NWD1 | GRCh38.p7 | 19:16798467 | AACACAAAAATTAGC[C/G/T]GGGCGTCATGGCATG | 284434 |
rs193920843 | snp | A/G | 1.65053e-05 | 0.0028727 | NWD1 | 19 | allele_origin=G(somatic)/A(germline) | 19:16800094 | CCGCAGTGTCCCACA[A/G]TGGAAGCTACGTCTA | 284434 |
rs199535319 | in-del | -/TTC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16778477 | TTTCTTTTCTTTTCT[-/TTC]TTCTTCTTCTTCTTC | 284434 |
rs199576385 | snp | A/G | 0.00199792 | 0.0315431 | synonymous-codon, missense | NWD1 | GRCh38.p7 | 19:16797826 | AGACATGGTGGAGAC[A/G]GCTGTTTTTGGTACT | 284434 |
rs199586141 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815413 | AAAGCAAAAAGAATA[C/T]GTTTGCTGGTGTATA | 284434 |
rs199631115 | snp | A/G/T | 3.31429e-05 | 0.0040707 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749406 | TGGTGAACCCCAAGA[A/G/T]CAAGACTCACGCCTG | 284434 |
rs199634191 | in-del | -/A | 0.125528 | 0.21681 | intron-variant | NWD1 | GRCh38.p7 | 19:16738628 | TATTTTCTGAGATCT[-/A]TTTTCTGAGACCTAA | 284434 |
rs199638880 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16768601 | TAGGGGCCTGTGAAT[A/T]AAGACAGCTTAACAG | 284434 |
rs199649604 | in-del | -/ATCT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754023 | TCATCTCTATCTTCC[-/ATCT]ATCCATCCATCCATC | 284434 |
rs199652995 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764369 | ATCTTCTGTCCATCC[A/G]TCCATCCATCCATCC | 284434 |
rs199657864 | snp | C/G | | | intron-variant, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800439 | CTTGCGAGGCTGAGG[C/G]AGAATTGTTTGAACC | 284434 |
rs199666059 | in-del | -/T | 0.0603597 | 0.1629 | intron-variant | NWD1 | GRCh38.p7 | 19:16797195 | AAAAAAAAAAAAAAA[-/T]TGATGAGTGATTACA | 284434 |
rs199667260 | in-del | -/ATC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787905 | ATAATAATAATAATA[-/ATC]ATCATCATCATCATC | 284434 |
rs199679446 | in-del | -/CATC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754508 | ATCCATCCATCCATC[-/CATC]ATCTCTATCTTCCAT | 284434 |
rs199690393 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787916 | AATAATCATCATCAT[A/C]ATCATCATCATCATC | 284434 |
rs199698658 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790646 | TTAAAAAAAAATAAA[-/T]AAATAAATAAATAAA | 284434 |
rs199704149 | snp | G/T | 0.153997 | 0.230832 | intron-variant | NWD1 | GRCh38.p7 | 19:16766558 | TGTTCTGTTTGGTTT[G/T]GTTTTAATTATAGCA | 284434 |
rs199711287 | in-del | -/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16733802 | CACATCGGGAGACGG[-/C]GGTCCCTCCAGAAGC | 284434 |
rs199715274 | snp | A/C | 0.000104686 | 0.0072341 | intron-variant, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800170 | GGCAGAAGGTTGGTA[A/C]GGTATAAGTATGGTC | 284434 |
rs199751769 | in-del | -/A | 0.0759472 | 0.179459 | intron-variant | NWD1 | GRCh38.p7 | 19:16782109 | AAAAAAAAAAAAAAG[-/A]AAAAAAAAAAGAATC | 284434 |
rs199771656 | snp | A/G | 8.2633e-05 | 0.00642726 | missense, utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16799967 | CTGCTGGCCCGCGGC[A/G]GGGCTTTGGTGGCAT | 284434 |
rs199787462 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16730907 | TTTTTATTTTTCTTT[C/T]TTTCTTTTTTTTTTT | 284434 |
rs199821486 | snp | C/T | 0.000247829 | 0.0111289 | missense | NWD1 | GRCh38.p7 | 19:16791381 | TGGAAACTGCAGAGC[C/T]GGTATTCCATATCCT | 284434 |
rs199881002 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790642 | AACATTAAAAAAAAA[A/T]AAATAAATAAATAAA | 284434 |
rs199889372 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732598 | AATCCCTGGCTAGGG[-/A]ATTTTTTTTTTTTTT | 284434 |
rs199892003 | in-del | -/AAGG | 0.0524604 | 0.153226 | intron-variant | NWD1 | GRCh38.p7 | 19:16751498 | AGGAAGGAAGGAAGG[-/AAGG]GAGGAAGGAAGGAAA | 284434 |
rs199908020 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16785771 | ACATATATACAAAAA[A/C]AAATATATACATAAA | 284434 |
rs199917181 | in-del | -/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16737565 | CTGGTCTAGTTTTAA[-/G]GTTTTTTTTTTTTTT | 284434 |
rs199932301 | in-del | -/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16805876 | TTTCTTTCTTTTCTT[-/C]TTTTTTTTTTGAGAG | 284434 |
rs199936999 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16794790 | TTTCTATTATTTTTC[-/T]TTTTTTTTTTAAATA | 284434 |
rs199988216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16782533 | CTGAATCAAATTTCT[A/G]TTAGAGATGACATAT | 284434 |
rs199994070 | in-del | -/ATTTTATTTT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16760230 | AACATAAAATTCACC[-/ATTTTATTTT]ATTTTATTTTATTTT | 284434 |
rs199995129 | snp | C/T | 0.000164756 | 0.00907472 | stop-gained | NWD1 | GRCh38.p7 | 19:16808017 | GAGACCCACAGGAGC[C/T]GAGTTGCCTGTGTGG | 284434 |
rs200044167 | in-del | -/G | 0.0513262 | 0.151752 | intron-variant | NWD1 | GRCh38.p7 | 19:16742569 | GGAGAGCTGGACTTA[-/G]GGTCCTCTTAGCCCT | 284434 |
rs200127031 | snp | A/G | 0.000148291 | 0.0086095 | missense | NWD1 | GRCh38.p7 | 19:16807858 | CCCTGCCCGGTCATC[A/G]ATGGGCCAAGATACA | 284434 |
rs200135465 | in-del | -/GGACCACAGGG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16794028 | CCTCCTGAGTAGCTG[-/GGACCACAGGG]GTGTACCACCATGCC | 284434 |
rs200226720 | in-del | -/ATCC | 0.373196 | 0.217538 | intron-variant | NWD1 | GRCh38.p7 | 19:16773940 | TTCATCCATCCATCT[-/ATCC]ATCCATCCATCCATC | 284434 |
rs200246636 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16728300 | TTTTTTTTTTTTTTT[C/T]CTGAGATGGAGTCTC | 284434 |
rs200259485 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NWD1 | GRCh38.p7 | 19:16737817 | TATCTACTAAAAAAT[C/T]AGCTGGGCATGGTGG | 284434 |
rs200282926 | snp | A/G | 3.29663e-05 | 0.00405981 | missense | NWD1 | GRCh38.p7 | 19:16808065 | CAGCTGGTGGTCAGC[A/G]GGTCTGAGGATGCCC | 284434 |
rs200324504 | snp | C/T | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748215 | TCTCAAACTCCTGAC[C/T]TCAGGTGATCTGCCC | 284434 |
rs200342520 | in-del | -/TG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16752217 | TCTCAGTTTTAGGGT[-/TG]TTTTTTTTTTTTCTC | 284434 |
rs200357203 | in-del | -/GAAG | 0.0861826 | 0.188849 | intron-variant | NWD1 | GRCh38.p7 | 19:16751838 | AAAGAAAGAGAAAGA[-/GAAG]GAAGGAAGGAAGGAA | 284434 |
rs200366855 | snp | A/T | 0.00199792 | 0.0315431 | missense | NWD1 | GRCh38.p7 | 19:16797786 | GGGGCTTTCGCCGAT[A/T]CATGGCCATGGATCT | 284434 |
rs200373638 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787882 | TAATAATAACAATAA[C/T]AATAATAATAATAAT | 284434 |
rs200410922 | in-del | -/C/CTTTTTTTTTTT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16778496 | CTTCTTCTTCTTCTT[-/C/CTTTTTTTTTTT]TTTTTTTTTTTTGTT | 284434 |
rs200453193 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16735844 | AGAAGGAAGGAAGGA[A/C]GGAAGGAAGGAAGGA | 284434 |
rs200501347 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16760272 | TTTATTTTATTTTAT[G/T]TTATGTATTTTGAGA | 284434 |
rs200505308 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16801076 | TGAGGTCGGGAGTTC[A/G]AGACCAGCCTGACCA | 284434 |
rs200511332 | in-del | -/AAT | 0.40386 | 0.197046 | intron-variant | NWD1 | GRCh38.p7 | 19:16788233 | AAAACTTCATCTCAA[-/AAT]AATAATAATAATAAT | 284434 |
rs200522149 | snp | C/T | 0.0029954 | 0.038584 | intron-variant | NWD1 | GRCh38.p7 | 19:16759197 | AGACATGAGATGTGC[C/T]TCAAAGCCCCACTGG | 284434 |
rs200555574 | in-del | -/AT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16775305 | CAGATGTTGTAAAAA[-/AT]AAAATGGCCAAAATA | 284434 |
rs200588792 | in-del | -/CCATCCAC | 0.0494327 | 0.149241 | intron-variant | NWD1 | GRCh38.p7 | 19:16774467 | GTTCCACTGTTCCAT[-/CCATCCAC]CCATCCACCCATCCA | 284434 |
rs200592263 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16783121 | ACTACAATCTTGACA[A/T]CCCAGGTTCAAGCAA | 284434 |
rs200598722 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16808544 | ACAGACACTCCGTTT[-/A]AAAAAAAAAGAAAAG | 284434 |
rs200643172 | snp | A/G | 0.000116189 | 0.0076211 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749487 | TCCTCACACGCCTCC[A/G]TGAGCTGGATACGGC | 284434 |
rs200659024 | in-del | -/CCAT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754874 | CTTCCATCCATCCAT[-/CCAT]TCATCCACCCATCCG | 284434 |
rs200667323 | in-del | -/TC | 0.0810805 | 0.184299 | intron-variant | NWD1 | GRCh38.p7 | 19:16797325 | AGGGGTTCCAAAACA[-/TC]TCTTTTTTTTTTTTT | 284434 |
rs200698221 | in-del | -/AT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751241 | AAAAAAAAAAAAAAA[-/AT]GCAATAAACTTGGGT | 284434 |
rs200716676 | in-del | -/TCCATCCA | 0.172351 | 0.237636 | intron-variant | NWD1 | GRCh38.p7 | 19:16754463 | CCATCATCTCTATTT[-/TCCATCCA]TCCATCCATCCATCC | 284434 |
rs200720324 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782108 | CAAAAAAAAAAAAAA[A/G]AAAAAAAAAAAGAAT | 284434 |
rs200735264 | snp | C/T | 0.00384688 | 0.043688 | missense | NWD1 | GRCh38.p7 | 19:16750057 | CAGCTTGCTCGGGGG[C/T]ACTGGGGGTTTTGGA | 284434 |
rs200750479 | in-del | -/AAA | 0.0410537 | 0.137264 | intron-variant | NWD1 | GRCh38.p7 | 19:16738001 | AAAAGAAAAGAAAAG[-/AAA]AGAAAAGAAATTCTA | 284434 |
rs200758864 | in-del | -/AC/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16746692 | AAAAACAAAAAACAA[-/AC/C]CAAAAAAAAACAGTC | 284434 |
rs200763762 | snp | A/G | 0.00299555 | 0.038585 | missense | NWD1 | GRCh38.p7 | 19:16807642 | TGTCTGGAGGTTGCT[A/G]AGCAGCGCAAGCTCC | 284434 |
rs200792163 | snp | A/G | 0.00032987 | 0.0128385 | missense | NWD1 | GRCh38.p7 | 19:16779457 | TCCACATGCTAACTG[A/G]ACACACAGGTGAGAC | 284434 |
rs200835395 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790643 | ACATTAAAAAAAAAT[A/T]AATAAATAAATAAAT | 284434 |
rs200849201 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16736193 | TTCCTTCTTTCCTTC[C/T]TTCCTTCCTTCCTTC | 284434 |
rs200852831 | in-del | -/CAAA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16812702 | AAACAAACAAACAAA[-/CAAA]AAACCCAAGAAAAAG | 284434 |
rs200870236 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16735759 | CGCTTGAACCCATTA[C/G]GCAAAATTTACAATG | 284434 |
rs200876173 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16739190 | TTAATGAGTTTCCAA[A/G]AAAAAAAAAAAGGAG | 284434 |
rs200896265 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16730911 | TATTTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 284434 |
rs200901631 | in-del | -/CCT | 0.00597247 | 0.0543191 | intron-variant | NWD1 | GRCh38.p7 | 19:16793658 | CTCGGCTCACTGAAA[-/CCT]CCACCTCCCAGCTTC | 284434 |
rs200918930 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16725970 | TGTTTGTTTTTTTTT[G/T]CTTTTTTTTTAGACA | 284434 |
rs201105182 | snp | C/T | 6.83819e-05 | 0.0058469 | missense | NWD1 | GRCh38.p7 | 19:16789186 | ATTCAGCATCTGGCT[C/T]AAAGGTAACAAACAT | 284434 |
rs201110661 | in-del | -/G | 0.0115144 | 0.0749975 | intron-variant | NWD1 | GRCh38.p7 | 19:16750819 | CTAAATACAGTTTTT[-/G]TTTGTCAACTATACC | 284434 |
rs201116385 | snp | A/G | 0.000149282 | 0.00863822 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749370 | TCCTCAAGACCCACC[A/G]CCTGCCGTGGAGCCG | 284434 |
rs201125560 | in-del | -/TCCA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764362 | TCCACCCATCTTCTG[-/TCCA]TCCATCCATCCATCC | 284434 |
rs201180088 | snp | C/T | 0.00199791 | 0.031543 | intron-variant | NWD1 | GRCh38.p7 | 19:16789205 | GGTAACAAACATATG[C/T]CCTGTTTGTAAAGGA | 284434 |
rs201191025 | in-del | -/AC | 0.0744748 | 0.178019 | intron-variant | NWD1 | GRCh38.p7 | 19:16785770 | TACATATATACAAAA[-/AC]AAATATATACATAAA | 284434 |
rs201205274 | snp | A/G | 0.00199805 | 0.0315441 | missense | NWD1 | GRCh38.p7 | 19:16789092 | CAGGAGAAATTTACC[A/G]TTTGGGATGGAGGCT | 284434 |
rs201219354 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16785904 | GAGTCCCACTCTGTC[A/G]CCCAGGCTGGAGTGC | 284434 |
rs201229655 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16810041 | GTCTGGGCAAAAGGA[-/T]TTTTTTTGTGTGTGT | 284434 |
rs201268907 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16804992 | CATGCCTGACTCCTG[C/G]AGACTTTAAAATTTT | 284434 |
rs201290991 | snp | C/G | 0.000100112 | 0.00707431 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16762123 | TGTGGGGAAACCACT[C/G]AACTTGGACCGAAAG | 284434 |
rs201309637 | snp | A/G/T | 0.000531433 | 0.0162923 | synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749518 | CGGACAGGAGTTGGC[A/G/T]TGGCTCTACCAAGAG | 284434 |
rs201334354 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787904 | AATAATAATAATAAT[A/C]ATCATCATCATCATC | 284434 |
rs201371479 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16772357 | GTGACAGAGTAAGAC[C/T]CTGTCTCTAAAAAAA | 284434 |
rs201376808 | in-del | -/CATC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754703 | ATCCATCATCTCTAG[-/CATC]CATCCATCCATCCAT | 284434 |
rs201390129 | in-del | -/AAAAAAAAAAAAAA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782094 | GTGAGACTCTGTCTC[-/AAAAAAAAAAAAAA]GAAAAAAAAAAAGAA | 284434 |
rs201427361 | snp | C/G/T | 0.00199803 | 0.031544 | missense | NWD1 | GRCh38.p7 | 19:16759242 | ACGGTCTCTCGGAGG[C/G/T]GGAGCTGAAGGATGT | 284434 |
rs201479203 | snp | C/T | 0.000292099 | 0.0120816 | stop-gained, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744538 | CTGGAGCTGGTGGCA[C/T]GATACTTCCAGAGGG | 284434 |
rs201479345 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16767381 | GCACTTTGGGAGGCC[A/G]AGGCAGGCAGATCAC | 284434 |
rs201532369 | in-del | -/GGAAG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16777147 | GAGGGGAAAGGGGAG[-/GGAAG]GGAAGGGGAAGGGAA | 284434 |
rs201533207 | in-del | -/ATTTTATTTTATTTT | 0.42666 | 0.176893 | intron-variant | NWD1 | GRCh38.p7 | 19:16760230 | AACATAAAATTCACC[-/ATTTTATTTTATTTT]ATTTTATTTTATTTT | 284434 |
rs201556939 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782109 | AAAAAAAAAAAAAAG[A/G]AAAAAAAAAAGAATC | 284434 |
rs201567758 | in-del | -/C | 0.0221141 | 0.102801 | intron-variant | NWD1 | GRCh38.p7 | 19:16798950 | AATTAAAAAAAAAAA[-/C]AACATTAAAAGTTTT | 284434 |
rs201592521 | in-del | -/A | 0.0115144 | 0.0749975 | intron-variant | NWD1 | GRCh38.p7 | 19:16794371 | CTCCATCTCAAAAAC[-/A]AAAAAAAATAAAAAT | 284434 |
rs201594879 | snp | C/T | 1.67897e-05 | 0.00289733 | synonymous-codon, utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16799933 | GGACATCCTGGAAGG[C/T]GTCGGGGCCCCCGTG | 284434 |
rs201596843 | snp | G/T | | | downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16818008 | TTGAAAAAGAGTTTG[G/T]TTGCTAAGAAAGTTT | 284434 |
rs201607833 | in-del | -/AATAATAATAAT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16788233 | AAAACTTCATCTCAA[-/AATAATAATAAT]AATAATAATAATAAT | 284434 |
rs201623864 | in-del | -/TCC | 0.0611083 | 0.163768 | intron-variant | NWD1 | GRCh38.p7 | 19:16761358 | TTCTTTCTCTTTCTT[-/TCC]TCTTTCTTTCCTTCT | 284434 |
rs201665040 | snp | C/G | 1.65094e-05 | 0.00287305 | utr-variant-3-prime, missense | NWD1 | GRCh38.p7 | 19:16815238 | AGGAGCTAGTTGCAG[C/G]TGCAGGAGCTCCCCA | 284434 |
rs201716593 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16736197 | TTCTTTCCTTCTTTC[C/T]TTCCTTCCTTCTTTC | 284434 |
rs201791536 | in-del | -/AGG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751865 | AAAGAAAAAAAAAGA[-/AGG]AAAGAAGAGATAAAG | 284434 |
rs201801544 | snp | A/G | 4.9476e-05 | 0.00497348 | missense | NWD1 | GRCh38.p7 | 19:16765070 | GCCGGGGCATCTCTG[A/G]GGGCATTGAAGACCT | 284434 |
rs201834118 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16725431 | TACAGTGAGCTATGA[A/T]CACACCACTGCACTC | 284434 |
rs201834613 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16768600 | ATAGGGGCCTGTGAA[A/T]TAAGACAGCTTAACA | 284434 |
rs201835251 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16753869 | CATCCATCCATCCAT[C/T]CATCAATTCGACCTT | 284434 |
rs201853862 | in-del | -/AAGG | 0.0170251 | 0.090679 | intron-variant | NWD1 | GRCh38.p7 | 19:16751433 | AGAGTGAAAGAAGGA[-/AAGG]AAGGAAGGAAGGAGA | 284434 |
rs201863745 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16733805 | ATCGGGAGACGGCGG[-/T]CCCTCCAGAAGCACA | 284434 |
rs201898485 | snp | C/T | 0.000286098 | 0.0119569 | synonymous-codon, intron-variant | NWD1 | GRCh38.p7 | 19:16794549 | TGAGTCCCTCCTCGC[C/T]GCAGGTAGCGTTTAG | 284434 |
rs201955025 | in-del | -/T/TT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16805873 | TTTTTCTTTCTTTTC[-/T/TT]TTCTTTTTTTTTTGA | 284434 |
rs202035631 | in-del | -/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16741370 | TTTTGTTTTTGTGTT[-/G]TTTTTTTTTTTTTTT | 284434 |
rs202038795 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | NWD1 | GRCh38.p7 | 19:16735825 | GAAGGAAGGAAGGAA[A/G]GAAAGAAGGAAGGAA | 284434 |
rs202056350 | snp | A/G | 0.00013501 | 0.00821502 | missense | NWD1 | GRCh38.p7 | 19:16750246 | GTGGGAACCCAGGGC[A/G]GCTGAGGCTGGCGTT | 284434 |
rs202142885 | snp | A/G | 0.000397601 | 0.0140941 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749387 | CTGCCGTGGAGCCGC[A/G]ACTTGGTGAACCCCA | 284434 |
rs202221737 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16777810 | GAGGGAAGGGAAGGG[-/A]AAGGGGAGGGAAGGG | 284434 |
rs202225653 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16747039 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTTGC | 284434 |
rs202236781 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16793061 | AAAAAATTAAAAAAT[A/T]AAAAAAAAAAGAAAA | 284434 |
rs267605334 | snp | C/T | | | missense | NWD1 | GRCh38.p7 | 19:16750125 | TGGGAGGTGAAGCCC[C/T]TTTCCGGAAACCAAG | 284434 |
rs267605335 | snp | C/T | | | synonymous-codon | NWD1 | GRCh38.p7 | 19:16765053 | CATGAGCTGGATTTC[C/T]TGCCGGGGCATCTCT | 284434 |
rs267605336 | snp | C/T | | | missense | NWD1 | GRCh38.p7 | 19:16807697 | TCGTCCTTGTGTTCC[C/T]CCTGAATTCCAGGCA | 284434 |
rs267605337 | snp | A/G | | | utr-variant-3-prime, stop-gained | NWD1 | GRCh38.p7 | 19:16815200 | CAAGAAGGCAATGTG[A/G]ATGGTCAAATCCAGG | 284434 |
rs267605338 | snp | C/G/T | 1.64806e-05 | 0.00287054 | NWD1 | 19 | allele_origin=T(somatic)/C(germline) | 19:16815206 | GGCAATGTGGATGGT[C/G/T]AAATCCAGGCAGAGA | 284434 |
rs367553720 | snp | A/G | 8.43277e-05 | 0.00649282 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750259 | GCGGCTGAGGCTGGC[A/G]TTTGAGGAAGCCCGG | 284434 |
rs367554820 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16746844 | TTAAACATAAGTGGA[C/T]CATCAGTCACAAAGG | 284434 |
rs367589031 | in-del | -/AAAG | 0.00598558 | 0.054378 | intron-variant | NWD1 | GRCh38.p7 | 19:16735521 | CCTGACCAAAAAAAA[-/AAAG]AAAGAAAGAAAGAAA | 284434 |
rs367619006 | snp | A/G/T | 4.97363e-05 | 0.00498659 | missense | NWD1 | GRCh38.p7 | 19:16791596 | GGAAAGCTTGTTACC[A/G/T]GGTTTAGCAATGGCT | 284434 |
rs367623956 | snp | C/G | 1.71555e-05 | 0.00292873 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749646 | ACAGCAAGCAGCACA[C/G]CCCCCTGGTACTCTT | 284434 |
rs367624158 | in-del | -/TGTTTTGTTT | 0.0988009 | 0.199095 | intron-variant | NWD1 | GRCh38.p7 | 19:16723677 | TTTTACAGCTTTTTC[-/TGTTTTGTTT]TGTTTTGTTTTGTTT | 284434 |
rs367669456 | snp | C/T | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817237 | CCCGGGAGGCGGAGG[C/T]TGCAGTGAGCTGAGA | 284434 |
rs367694328 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16734629 | TCACCCAGGCTGGAG[A/T]GCAGGCATGCAATCA | 284434 |
rs367735604 | in-del | -/TTCT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16736206 | TCTTTCCTTCCTTCC[-/TTCT]TTCCTTCCTTCCTTC | 284434 |
rs367752961 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16810677 | CTGAGGTGGGAGGAT[C/T]GATTGAGCCCTGGAG | 284434 |
rs367757045 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16784217 | TAAAAAGAAAAAAAA[A/G/T]AAAAGAAAAATTAAG | 284434 |
rs367763510 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16784656 | GAGCAGTCGGCTGGG[C/T]GCGGTGGCTCACGCC | 284434 |
rs367772619 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16773974 | CATCCATCCATCCAT[C/T]CATTAATTCACCTTC | 284434 |
rs367876330 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16801882 | TGTTAGTTCTCGCGA[A/G]GTTGTTAAAAAGAAC | 284434 |
rs367891564 | in-del | -/GGA | 0.00636936 | 0.0560724 | intron-variant | NWD1 | GRCh38.p7 | 19:16798146 | TTGTGCCTTCAGAGT[-/GGA]GCAGGGTTGTGGGGG | 284434 |
rs367915299 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | NWD1 | GRCh38.p7 | 19:16763820 | CAGTCTCCCTTCTCC[C/T]CTGCCAGGTGGCCCC | 284434 |
rs367939338 | snp | A/C | 1.64754e-05 | 0.00287009 | missense | NWD1 | GRCh38.p7 | 19:16791447 | TGCTGGCCTCCCAGG[A/C]CACACTGCTGACAGT | 284434 |
rs367979080 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16762237 | CTCGAAATGTCCTCC[C/T]GACCTACTTCTCCTT | 284434 |
rs368043372 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16728258 | AGAACAGAGTATTAT[A/G]GAACATTTGCTGGGT | 284434 |
rs368064624 | snp | A/C | 6.68494e-05 | 0.00578102 | missense | NWD1 | GRCh38.p7 | 19:16750164 | ATGATCCAACTCCTG[A/C]TGGCAGCTGCAAGGA | 284434 |
rs368074108 | in-del | C/TT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16737576 | TTTAAGTTTTTTTTT[C/TT]TTTTGAGATGGGTCT | 284434 |
rs368114098 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16808325 | GAGGCTGAGGCAGGC[A/G]GATCACCTGAGATCG | 284434 |
rs368145213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16773342 | AGTCTCCCCAGCATA[A/G]CAAAAATCCCAGCAG | 284434 |
rs368145504 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16742236 | AAAAATTAGCCAGGC[A/G]TGGTGGCTCACGCCT | 284434 |
rs368177197 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16752211 | GCCTCTTCTCAGTTT[A/T]AGGGTTGTTTTTTTT | 284434 |
rs368195388 | snp | A/G | 3.29924e-05 | 0.00406142 | missense | NWD1 | GRCh38.p7 | 19:16765058 | GCTGGATTTCCTGCC[A/G]GGGCATCTCTGGGGG | 284434 |
rs368196501 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16722425 | TCCCTGAGTAGCTGG[G/T]ATTACAGGCATGAAC | 284434 |
rs368201346 | snp | C/T | 3.29794e-05 | 0.00406061 | missense, upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749249 | CACATCCTTGAAGAC[C/T]GCGCCCTTAGGATGG | 284434 |
rs368378937 | snp | C/T | | | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16719292 | AGGCATGCGTCACCA[C/T]GCCCAGCTAATTTTT | 284434 |
rs368401489 | snp | A/C | | | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16738269 | AGTAAAGAGGGAAAA[A/C]GTAAAGAAAAGTACC | 284434 |
rs368491608 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16809033 | TGCTCTCTAGCCTGG[A/G]TGATAGAGCAAGGCC | 284434 |
rs368516100 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16784242 | ATTAAGTATACAGGA[G/T]CACCTGTAGTCCCAG | 284434 |
rs368521595 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16772067 | TCCTCTGATCCTACT[C/T]TTATTGAAAAGGTTG | 284434 |
rs368529299 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16723128 | AGCCTCAACCTCCTG[C/T]GCTCAAGTGATTCTC | 284434 |
rs368537202 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16802207 | GAATCGCTTGAGCCC[A/G]GCAGGCAGAGGTTGC | 284434 |
rs368538247 | snp | A/G | 0.0001001 | 0.0070739 | synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749584 | TCAGACCTTCTGCGG[A/G]CGCCAGGAACTCCTG | 284434 |
rs368551155 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16808834 | TGCAGTGGCTCACCC[A/G]GCACTTTGGGAGGCC | 284434 |
rs368570683 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16758555 | GTGCAGGGATTACAG[A/G]TGTGAGCCACCACGC | 284434 |
rs368571834 | snp | A/G | 6.78933e-05 | 0.00582598 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750307 | CGTGCCTGTCCCGCT[A/G]GCCACCACCGCAGAG | 284434 |
rs368592850 | in-del | -/TGAGGCAGAGTCTCTCTCTGTT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16723071 | TCTTATTTTATTTTT[-/TGAGGCAGAGTCTCTCTCTGTT]GCCCAGTGGTGGCTC | 284434 |
rs368603365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16742989 | GCCATCTTGGCTCAC[C/T]GCAACCTTCGCCTCC | 284434 |
rs368633239 | snp | A/C | 3.29554e-05 | 0.00405914 | missense | NWD1 | GRCh38.p7 | 19:16779352 | CTGCAGGCATCACCG[A/C]CATGGCATGGGGTGT | 284434 |
rs368639253 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16775988 | ATGTGGTCTTTGTGC[A/G]GATAACTATGTACTC | 284434 |
rs368646576 | in-del | -/AAATAAAAATAA | 0.296873 | 0.245566 | intron-variant | NWD1 | GRCh38.p7 | 19:16802286 | CAAAAATAAATAAAT[-/AAATAAAAATAA]AAATAAAAATAAAAA | 284434 |
rs368669899 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750034 | CCCGAGGGTGCACCT[C/T]ATCCTCTCAGCTTGC | 284434 |
rs368694270 | snp | G/T | 1.64738e-05 | 0.00286995 | utr-variant-3-prime, stop-gained | NWD1 | GRCh38.p7 | 19:16815129 | GGTTATCTGATCCGA[G/T]AGAATTTCCAGTGCC | 284434 |
rs368774906 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16767943 | AGCAGAATGTCCTCA[A/G]GTTTCATCCACATTG | 284434 |
rs368799777 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16780760 | CCTCCTGGGCTCAAG[A/C]AATCCTCCCATCTCA | 284434 |
rs368830699 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | NWD1 | GRCh38.p7 | 19:16734491 | AGTGAGCCAAGATTG[C/T]GCCACTGCACTCCAG | 284434 |
rs368856625 | in-del | -/CCATCCATCCATCCAT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16773962 | CATCCATCCATCCAT[-/CCATCCATCCATCCAT]TAATTCACCTTCCTA | 284434 |
rs368859469 | snp | C/T | 0.00010284 | 0.00717004 | missense | NWD1 | GRCh38.p7 | 19:16807676 | TTACGGGCCTCGTGT[C/T]GGGGGTCGTCCTTGT | 284434 |
rs368888574 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16798988 | CAGACCCTCTAAAAA[A/G]GGTTTACAGGGCACC | 284434 |
rs368908194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16789866 | GGGACTACAGGCGCA[C/T]GCCACCACGCCCAGC | 284434 |
rs368939428 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16811389 | AGGAGTTCGAGACCA[C/G]CCTGACCAACATGGT | 284434 |
rs368980533 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16752301 | GGTGGTCAACCCAAC[A/G]AGGAGGTCTTTCTGC | 284434 |
rs368993993 | in-del | -/TTCT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16738014 | AGAAAAGAAAAGAAA[-/TTCT]AGAGCAGAGGCCAAC | 284434 |
rs369009279 | in-del | -/TTATTTATTTAT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16755687 | CCACCACATCCAGCC[-/TTATTTATTTAT]TTATTTATTTATTTA | 284434 |
rs369139939 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NWD1 | GRCh38.p7 | 19:16728851 | CGGGAGGCTGAGGCA[A/G]GAGAATGGCGTGAAC | 284434 |
rs369146666 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16803344 | CAGACTTAGACAGGC[C/G]CCAGCTCCTAATACC | 284434 |
rs369163419 | snp | C/T | 0.0010202 | 0.0225623 | intron-variant | NWD1 | GRCh38.p7 | 19:16763994 | CTGGTGACTGCACCA[C/T]GCTCCAGTCTTCTAG | 284434 |
rs369215847 | in-del | -/CC | 0.00143697 | 0.026766 | intron-variant | NWD1 | GRCh38.p7 | 19:16762165 | GGACCCCCATTCCCC[-/CC]ACCTGCAACCTCCAC | 284434 |
rs369248613 | snp | C/T | 0.000312213 | 0.0124904 | synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749779 | GACGTCACAAATGAG[C/T]TCAGATGCCCGTGGC | 284434 |
rs369322052 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16781183 | TGAAGAGAGATAGAC[A/G]AGGGTCGGGACTAGG | 284434 |
rs369331492 | in-del | -/GGCTAAGAATTTCCTTCCTTTTCAA | 0.0962929 | 0.197165 | intron-variant | NWD1 | GRCh38.p7 | 19:16768292 | TGAGCTACCATGCCT[-/GGCTAAGAATTTCCTTCCTTTTCAA]GGCTAAGAATTTCCT | 284434 |
rs369331787 | snp | A/C/G | 0.00676944 | 0.0578265 | intron-variant | NWD1 | GRCh38.p7 | 19:16762292 | TTCTACTGTCCCCCC[A/C/G]ACTCCTTTTTTTTTT | 284434 |
rs369335593 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16723262 | GGGGTACAGTGTTGC[A/G]ATCTTGGCTCACTGC | 284434 |
rs369352623 | snp | A/G | 1.64882e-05 | 0.00287121 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16759237 | CAGACACGGTCTCTC[A/G]GAGGCGGAGCTGAAG | 284434 |
rs369384040 | snp | A/G | 1.65086e-05 | 0.00287298 | intron-variant | NWD1 | GRCh38.p7 | 19:16788938 | AGTTGCAAGGCCAAA[A/G]TGTTCCCAGCTAATA | 284434 |
rs369400102 | snp | G/T | 1.71252e-05 | 0.00292614 | intron-variant | NWD1 | GRCh38.p7 | 19:16797704 | CCTCTGGACATGAGA[G/T]GTGTAACCCCAGTTC | 284434 |
rs369408879 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16765438 | TCCTGGGTTCAAATG[A/C]TCCTCCCACCTCAGC | 284434 |
rs369413529 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16810394 | AGTGAGCCGAGAACA[C/T]GCCACTACACTCCAG | 284434 |
rs369418381 | in-del | -/ATCATCATCATC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787905 | ATAATAATAATAATA[-/ATCATCATCATC]ATCATCATCATCATC | 284434 |
rs369427420 | in-del | -/TCTA | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16764530 | CCATCCATCCATCAT[-/TCTA]TCTATCTATCCATGC | 284434 |
rs369572391 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16799776 | GCCTCCCAAAGTGTT[C/G]GGATTACAGGCGTGA | 284434 |
rs369581735 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16808624 | TTTCATTTTTTTTTT[-/T]AAAGAGACAGGGACC | 284434 |
rs369618174 | in-del | -/TTTGTTTA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16743680 | TTATTTATTAGTTTG[-/TTTGTTTA]TTTATTTATTTATTT | 284434 |
rs369622682 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16768588 | TTATGTTCAGTGATA[A/G]GGGCCTGTGAATTAA | 284434 |
rs369631370 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16724275 | AAGGTGGATATTTTC[A/G]GCATTAATTTTGATC | 284434 |
rs369645531 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16746628 | TAGTGAGCTGAGATC[A/G]CACCACTGCACTCCA | 284434 |
rs369653343 | snp | C/G | 6.59098e-05 | 0.00574026 | intron-variant | NWD1 | GRCh38.p7 | 19:16812721 | CCCAAGAAAAAGAGA[C/G]ATCATATTGTCTGTT | 284434 |
rs369683569 | snp | A/G | 6.60589e-05 | 0.00574675 | intron-variant | NWD1 | GRCh38.p7 | 19:16759193 | CAGAAGACATGAGAT[A/G]TGCCTCAAAGCCCCA | 284434 |
rs369799191 | snp | A/G | 8.29208e-05 | 0.00643844 | missense | NWD1 | GRCh38.p7 | 19:16765145 | AGGTTGGCCTGGTCC[A/G]TGAAGCCCTCCAGCT | 284434 |
rs369806073 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16724491 | TCTCTCTGCCTCCAG[C/T]GGTGGTTTGCTACTG | 284434 |
rs369840737 | snp | A/G | 1.93631e-05 | 0.00311146 | intron-variant | NWD1 | GRCh38.p7 | 19:16762179 | CCACCTGCAACCTCC[A/G]CCCTGCCTGGCATTG | 284434 |
rs369850508 | snp | A/C | 0.000115457 | 0.00759706 | missense, upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749230 | GATCCAAGACCTCCA[A/C]AAACACATCCTTGAA | 284434 |
rs369938966 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16729585 | CAAAAAGTAAAAAAA[A/G]AAAAAAAATAGGCTG | 284434 |
rs369945542 | in-del | -/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16753239 | TTGGCATCAGGAGCC[-/C]ATATTTCTGTGACCA | 284434 |
rs369960762 | snp | A/G | 0.00015792 | 0.00888455 | intron-variant | NWD1 | GRCh38.p7 | 19:16794559 | CTCGCCGCAGGTAGC[A/G]TTTAGCTCTCATTTG | 284434 |
rs369969017 | snp | C/T | 0.000153988 | 0.00877328 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749727 | AGATGCCAAGGCTGC[C/T]GGGGCACAAGACAGT | 284434 |
rs369971209 | snp | C/T | | | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16717972 | CCCACCTCAACCTCC[C/T]GAGTAGTTGGGACTA | 284434 |
rs370000328 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16803159 | CTCATGAGACTTATT[C/T]GCTACCACAAGAACA | 284434 |
rs370130883 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16763275 | GCTTCTGACCATCCA[A/T]TCTGATTATGATTAT | 284434 |
rs370139689 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787406 | AGATGCTGAATCTTT[A/G]TAAAACTCAATTATC | 284434 |
rs370142566 | snp | A/C | 0.081446 | 0.184634 | intron-variant | NWD1 | GRCh38.p7 | 19:16722123 | GTCTCTTGAAAAAAA[A/C]AACAACAACAACAAC | 284434 |
rs370163821 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744984 | TCCTGGCACAGGGGC[C/G]GTATTAGTCTGTTCT | 284434 |
rs370214988 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16793638 | CTGGAATGCAGTGGC[A/G]CAATCTCGGCTCACT | 284434 |
rs370224393 | snp | C/T | 3.32364e-05 | 0.00407641 | missense | NWD1 | GRCh38.p7 | 19:16807736 | TATGCATTCCCCCTC[C/T]CGAGGCCCGGAAAGC | 284434 |
rs370261916 | snp | C/T | 8.24355e-05 | 0.00641957 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16763857 | TCTGTGGTTCTCACA[C/T]ACGGTTGCAAACCTG | 284434 |
rs370315881 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16721756 | CACTCTAAGCTGCAG[A/T]TTTCTCATCTGTTGA | 284434 |
rs370344246 | snp | A/G | 0.000418099 | 0.0144525 | intron-variant | NWD1 | GRCh38.p7 | 19:16791308 | AAACTTGTAGTCTAG[A/G]TCTCCTGCCAAGATG | 284434 |
rs370395393 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16797328 | GGTTCCAAAACATCT[C/T]TTTTTTTTTTTTTTT | 284434 |
rs370412217 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16763228 | TTCACCTAGCCTCTC[A/G]GTCTCTTGCCCTAGT | 284434 |
rs370470502 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16812584 | TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG | 284434 |
rs370525441 | snp | C/T | 0.000132404 | 0.00813539 | synonymous-codon, utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16799963 | GAGCCTGCTGGCCCG[C/T]GGCGGGGCTTTGGTG | 284434 |
rs370527271 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16771120 | TCCTGGGCAACATAG[A/C]GAGACCCTATCTCTG | 284434 |
rs370537897 | snp | C/T | 8.4912e-05 | 0.00651527 | intron-variant | NWD1 | GRCh38.p7 | 19:16815008 | TTTTCTCATTTGTGT[C/T]CTTCTCTTCACCCTT | 284434 |
rs370552099 | in-del | -/TCCATCCATCCATCCA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16773953 | CTATCCATCCATCCA[-/TCCATCCATCCATCCA]TCCATCCATTAATTC | 284434 |
rs370567653 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16745247 | CAGTATGGGGGAAAC[C/T]ATCCCCCATGATTCA | 284434 |
rs370569933 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732786 | ACTACAGACATGCAG[C/T]GCTATCCCTGGCTAA | 284434 |
rs370580609 | snp | A/G | | | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16719175 | AAGTCTTGCTCTGTC[A/G]CCCAGGCTGCAGTGC | 284434 |
rs370602439 | in-del | -/TATTTATT | 0.0581099 | 0.160244 | intron-variant | NWD1 | GRCh38.p7 | 19:16734735 | ACCACTACACCTGGC[-/TATTTATT]TATTTATTTATTTAT | 284434 |
rs370651242 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16742000 | CCTGTAGTCCCAGCT[A/T]CTGGGGAGGTAGAGG | 284434 |
rs370661839 | snp | G/T | 3.38816e-05 | 0.00411578 | missense, intron-variant | NWD1 | GRCh38.p7 | 19:16749896 | GGTCCAGTTTTTCCA[G/T]ACCCTCCTCCACACT | 284434 |
rs370676815 | snp | C/T | 1.64762e-05 | 0.00287016 | synonymous-codon, missense | NWD1 | GRCh38.p7 | 19:16797793 | TCGCCGATTCATGGC[C/T]ATGGATCTGGAACAT | 284434 |
rs370677494 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16742282 | CAGGAGGCTGAGGCC[A/G]GAGAATCACTTGAAC | 284434 |
rs370733277 | snp | C/G | | | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807770 | CAACTGCATGTCCCT[C/G]AGCAAGTGCGAGGAC | 284434 |
rs370743416 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16729381 | GGGCCCATATCAGGA[C/T]TATCACTCTCACGGT | 284434 |
rs370745466 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16784130 | AGATCACTTGAACCT[C/G]GGAGGTGGAGGTTGC | 284434 |
rs370747842 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748904 | CCCTGGACCAGCAAG[C/G]CTTGGCTTGTTGCAA | 284434 |
rs370864354 | snp | A/G | 1.64836e-05 | 0.0028708 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807824 | CATCGTCCTGGTGCT[A/G]GACATCACCTCCGGG | 284434 |
rs370896915 | in-del | -/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16801102 | ACCAACATGGAAAAA[-/C]CCCCACCTCCACTAA | 284434 |
rs370922918 | snp | A/G | 0.000116155 | 0.00761996 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749459 | CAGTTTGTGGTGAGG[A/G]CCAATCACCAGGTCC | 284434 |
rs370930324 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16813336 | TGAAGGTTCCTTCAT[C/T]AATATAAGAGGACAC | 284434 |
rs370933889 | snp | A/T | 1.78258e-05 | 0.00298539 | intron-variant | NWD1 | GRCh38.p7 | 19:16789202 | AAAGGTAACAAACAT[A/T]TGCCCTGTTTGTAAA | 284434 |
rs370951450 | snp | A/T | 1.6476e-05 | 0.00287014 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807980 | TCTTTACGAGTGTGC[A/T]ACTTCCAAAGCGTTT | 284434 |
rs370954307 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant | NWD1 | GRCh38.p7 | 19:16791345 | CCTCTTCATTATTCT[A/T]TTAGATCAATGCTTG | 284434 |
rs370979723 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | NWD1 | GRCh38.p7 | 19:16762169 | CCCCCATTCCCCACC[C/T]GCAACCTCCACCCTG | 284434 |
rs371000381 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16736909 | CTAATCAATCACAGA[A/C]CTCTTTCTGCAGAGC | 284434 |
rs371002480 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16757424 | GGACCAATGAGATCA[C/T]ACTCGCCAGAATAAG | 284434 |
rs371006476 | snp | C/T | 0.000281171 | 0.0118535 | intron-variant | NWD1 | GRCh38.p7 | 19:16763819 | GCAGTCTCCCTTCTC[C/T]TCTGCCAGGTGGCCC | 284434 |
rs371010210 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16800617 | TCTGGAGGCTGGGAA[G/T]TTCCAGATCAAAGTG | 284434 |
rs371111829 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16734117 | GAACTGCAAGCGTGC[A/G]GTTGCCAAGGAGACC | 284434 |
rs371131626 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16771368 | GGCACGAAAATTGCT[C/T]GAACCCGGGAGGCAG | 284434 |
rs371202996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16762499 | ACGGGGTTTCACCAC[A/G]TTGGCCATACTGGTC | 284434 |
rs371234235 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16810323 | TGTGCCTGTAATCCC[A/G]GCTACCCGGGAGGCC | 284434 |
rs371260908 | in-del | -/CTTCTTTC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16783024 | TTCTTTCCTTCTTTC[-/CTTCTTTC]TTTCTTTTCTTTCTT | 284434 |
rs371284842 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16802788 | GGCGCATCATTTGAG[A/G]TCAGGTGTTCGAGAC | 284434 |
rs371297297 | snp | A/C/T | 8.37997e-05 | 0.00647253 | missense | NWD1 | GRCh38.p7 | 19:16750183 | CAGCTGCAAGGAGGA[A/C/T]GCTGAGCCCGGTGCA | 284434 |
rs371321948 | snp | A/G | 1.64866e-05 | 0.00287106 | missense | NWD1 | GRCh38.p7 | 19:16808074 | GTCAGCGGGTCTGAG[A/G]ATGCCCTGCTGTGTC | 284434 |
rs371330107 | snp | A/G | 1.66416e-05 | 0.00288453 | intron-variant | NWD1 | GRCh38.p7 | 19:16791627 | CCATCTCTTTGGTAA[A/G]CACCTTTACTGACTA | 284434 |
rs371338220 | snp | A/C | 8.70224e-05 | 0.00659573 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749688 | GCATTGGAAAGACAG[A/C]CCTGATGTGCAAGCT | 284434 |
rs371339485 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16736177 | TTGGCAGTCTTTTTC[C/T]TTCCTTCTTTCCTTC | 284434 |
rs371348268 | snp | A/G | 6.65015e-05 | 0.00576596 | intron-variant | NWD1 | GRCh38.p7 | 19:16763948 | CAGGAGGTTCTGGGT[A/G]AGGGCTGCCCCCCAT | 284434 |
rs371383273 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16789875 | GGCGCACGCCACCAC[A/G]CCCAGCTAATTTTTG | 284434 |
rs371393507 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16729673 | GAGGAGTTTGAGACC[A/C]GCGTGGCCAACATGG | 284434 |
rs371397045 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16762357 | GCTGGAGTGCAATGG[C/T]GTGATCTCAGCTCAC | 284434 |
rs371438099 | snp | A/G | 0.000189552 | 0.00973346 | missense | NWD1 | GRCh38.p7 | 19:16773297 | CGGGAGGACCCCTCC[A/G]GGCAACTCTCAGCGG | 284434 |
rs371490507 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790639 | AGTAACATTAAAAAA[A/T]AATAAATAAATAAAT | 284434 |
rs371529896 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16753949 | CCTCCATCCTTCCAT[C/T]CATTCTCTCTAAATT | 284434 |
rs371530364 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16795160 | ACCCCATTTATTCAG[C/T]CTGTGGGGTCACATC | 284434 |
rs371538054 | snp | C/T | 0.0011702 | 0.0241605 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749251 | CATCCTTGAAGACTG[C/T]GCCCTTAGGATGGTG | 284434 |
rs371556775 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16793764 | GTATTTTTAGTAGAG[A/G]TGGGGTTTCACCATG | 284434 |
rs371569530 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16801945 | AAGATTGCTTGAGGC[C/T]GGGAGTTCAAGACCA | 284434 |
rs371577301 | in-del | -/TTT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782913 | ATCCTTCCTTCCTTC[-/TTT]CCTTCCTTTCCTTCC | 284434 |
rs371595131 | snp | C/G | 1.81912e-05 | 0.00301584 | intron-variant | NWD1 | GRCh38.p7 | 19:16799856 | GTCCACAGAAGATGT[C/G]AGATCTGCCCTCCTG | 284434 |
rs371634026 | snp | A/G | 3.33806e-05 | 0.00408524 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750055 | CTCAGCTTGCTCGGG[A/G]GCACTGGGGGTTTTG | 284434 |
rs371674563 | snp | G/T | 1.6894e-05 | 0.00290633 | missense | NWD1 | GRCh38.p7 | 19:16750281 | GAAGCCCGGAAATGG[G/T]CCTCTTTCACCGTGC | 284434 |
rs371725904 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | NWD1 | GRCh38.p7 | 19:16780184 | TTTTTGAGACGGAGT[C/T]TTGCTCTGTCGCCCA | 284434 |
rs371742233 | snp | A/G | | | downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16818320 | TAAAATAAAATTAAG[A/G]GATGCCGAAAAGCTC | 284434 |
rs371771832 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16814790 | AAAAACCTACACTAA[A/G]CACATGACCTGCATG | 284434 |
rs371786545 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16795981 | GACAATTGAAAAGTG[A/G]TAAGGACAGAGAATT | 284434 |
rs371795378 | snp | C/T | 0.000153988 | 0.00877328 | missense | NWD1 | GRCh38.p7 | 19:16765088 | GCATTGAAGACCTGC[C/T]GGATGACTTTGACCT | 284434 |
rs371809468 | snp | A/G | 4.94393e-05 | 0.00497164 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16791502 | GTGGAGCTCAGCTAC[A/G]GGAAAACTTCAGGGG | 284434 |
rs371883014 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16742452 | CGCTTTCATACTGAG[C/T]TCTGATCTCTCCCTT | 284434 |
rs371894240 | snp | C/T | 1.64762e-05 | 0.00287016 | missense | NWD1 | GRCh38.p7 | 19:16807982 | TTTACGAGTGTGCAA[C/T]TTCCAAAGCGTTTCC | 284434 |
rs371900926 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16811537 | TGCAGTGAGCCAAGA[C/T]CGTGATATTGCACTT | 284434 |
rs371904761 | snp | A/G | 3.35447e-05 | 0.00409527 | intron-variant | NWD1 | GRCh38.p7 | 19:16763975 | CCATCTCAGAGGACC[A/G]AGCCTGGTGACTGCA | 284434 |
rs371938960 | snp | C/T | 0.000168873 | 0.00918739 | missense | NWD1 | GRCh38.p7 | 19:16750272 | GCGTTTGAGGAAGCC[C/T]GGAAATGGGCCTCTT | 284434 |
rs371988369 | snp | C/T | 5.20702e-05 | 0.0051022 | synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749746 | GCACAAGACAGTGAC[C/T]GTCCTGCGGCTGCTG | 284434 |
rs372030240 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16780371 | CCGTGTTAGCCAGGA[C/T]GGTCTCAATCTCCTG | 284434 |
rs372039634 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16758279 | TATTTGTTCATGTAT[A/T]TATGTATTTATTTTA | 284434 |
rs372042757 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16735866 | AGGAAGGAAGGAAGG[-/A]AGGAAGGAAGGAAGG | 284434 |
rs372061937 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16790473 | AATTCGGGGGGTAGG[A/G]GGTAAGGGGAGGGAG | 284434 |
rs372072893 | in-del | -/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16733328 | AGTTCGAGACCAGCC[-/C]TGGCCAACATGGTGA | 284434 |
rs372127925 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16729473 | AGCCCTTCTCTGCCC[C/T]TCGATGTAAAGTAGA | 284434 |
rs372133402 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16758217 | GCAACCAAGAAACCG[C/T]ATTTTGAATTTTATT | 284434 |
rs372134481 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815414 | AAGCAAAAAGAATAC[A/G]TTTGCTGGTGTATAT | 284434 |
rs372161493 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16773975 | ATCCATCCATCCATC[A/C]ATTAATTCACCTTCC | 284434 |
rs372236718 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16735817 | GAAGGAAGGAAGGAA[A/G]GAAGGAAGGAAAGAA | 284434 |
rs372236959 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NWD1 | GRCh38.p7 | 19:16728323 | GGAGTCTCACTCTGT[C/T]GCCCAGGCTGGAGTG | 284434 |
rs372242399 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16784339 | TTACTATGCTCCAGC[A/C]GGGGTAACACAGCCA | 284434 |
rs372245046 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16724670 | CAGCCTTGAACTCAA[C/T]CCAGTGAGACCCCAT | 284434 |
rs372313482 | snp | C/G | 1.648e-05 | 0.0028705 | missense | NWD1 | GRCh38.p7 | 19:16779431 | GTGGGACATGGAAGA[C/G]CAGCATGTGATCCAC | 284434 |
rs372408350 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | NWD1 | GRCh38.p7 | 19:16763986 | GACCGAGCCTGGTGA[C/T]TGCACCACGCTCCAG | 284434 |
rs372430316 | snp | A/G | 3.36933e-05 | 0.00410433 | intron-variant | NWD1 | GRCh38.p7 | 19:16794564 | CGCAGGTAGCGTTTA[A/G]CTCTCATTTGGAGTA | 284434 |
rs372432096 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16775142 | TGCACTCCCCAGGCA[C/G]ATTATTTTCAAAATA | 284434 |
rs372452196 | in-del | -/CTC | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16814733 | CAACCTCTCTTCCTT[-/CTC]CTCCTTCAACAATAA | 284434 |
rs372464599 | snp | A/G/T | 4.94738e-05 | 0.00497341 | missense, upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749252 | ATCCTTGAAGACTGC[A/G/T]CCCTTAGGATGGTGG | 284434 |
rs372480386 | snp | A/G | 0.000153988 | 0.00877328 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749481 | ACCAGGTCCTCACAC[A/G]CCTCCGTGAGCTGGA | 284434 |
rs372493966 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NWD1 | GRCh38.p7 | 19:16793806 | AGTCTCAAACTCCTG[A/G]CCTCGAGTGATCCAC | 284434 |
rs372496965 | snp | C/G | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815995 | CAAGGTGCAAGAGCT[C/G]TGAGAGTGAGCCTTC | 284434 |
rs372506809 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16721684 | GTCCGTGGAGGAGAG[C/G]GGGTCTGACCCGCAC | 284434 |
rs372537753 | in-del | -/GAAG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16752002 | AAGGAAGGAAGGAAG[-/GAAG]CAAAAGCAAAAATAA | 284434 |
rs372544628 | snp | C/T | 4.98029e-05 | 0.00498988 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749480 | CACCAGGTCCTCACA[C/T]GCCTCCGTGAGCTGG | 284434 |
rs372571278 | snp | C/G/T | 1.64825e-05 | 0.00287071 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807833 | GGTGCTGGACATCAC[C/G/T]TCCGGGGACCCCTGC | 284434 |
rs372571415 | in-del | -/CAAA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16762574 | AAACAAACAAACAAA[-/CAAA]GTACAGAGTTATTGT | 284434 |
rs372596047 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16799257 | CTGAAGTGCAGTGGC[A/G]CAATCTCAGCTCACT | 284434 |
rs372617672 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16752420 | CAGCGTTTTGGGAGG[A/C]TGAGGTGGGAGGATC | 284434 |
rs372617867 | snp | C/T | | | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718834 | TGCCTGGGTGACTTG[C/T]GAGTTTTTGAGACAA | 284434 |
rs372632977 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16791799 | GCTCACTGCAACCTC[C/T]GCCTCTCGGGTTCAA | 284434 |
rs372645545 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16753150 | TCTCCCTCTGGGGTC[C/T]TCTCTGCACATCAAC | 284434 |
rs372677856 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16766760 | CTGGCTAATTTTTGT[A/G]TATTTTGTAGAGACG | 284434 |
rs372687783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16735920 | AGTGAGACAAGATTG[C/T]GCCACTGCACTCTAG | 284434 |
rs372698493 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16728931 | CCTGGGCAACAGAGC[A/G]TGACTCCATCTCAAA | 284434 |
rs372708412 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16812179 | CAGGTGTGGTGGCAC[A/C]CACTTGTAATCCCTG | 284434 |
rs372730827 | in-del | -/ATCCATCCATCCATCC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16773940 | TTCATCCATCCATCT[-/ATCCATCCATCCATCC]ATCCATCCATCCATC | 284434 |
rs372759931 | snp | A/C | 1.68812e-05 | 0.00290522 | intron-variant | NWD1 | GRCh38.p7 | 19:16797723 | TAACCCCAGTTCCTG[A/C]CGTTTCAGGCTTTGG | 284434 |
rs372770895 | in-del | -/CCAT | 0.0475351 | 0.146656 | intron-variant | NWD1 | GRCh38.p7 | 19:16764466 | ATGAGCTGGTTATAA[-/CCAT]CCATCCATCCATCCA | 284434 |
rs372805638 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764293 | ATGAGAGACCCTATC[A/T]GTCTGTCTGTCTATT | 284434 |
rs372811409 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16811412 | AACATGGTGAAACCT[C/T]ATCTCTCATAAAAAT | 284434 |
rs372894087 | snp | A/C/T | 5.07261e-05 | 0.00503596 | missense, synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749929 | CTCTTGCAGAAACTT[A/C/T]GAGTCTCTCGTGCTC | 284434 |
rs372955775 | snp | A/C | 0.0158469 | 0.0875917 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817338 | AGCCTCGGTGGCTCA[A/C]GCCTGTAATCCCAGC | 284434 |
rs373006092 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16789151 | GAACCTTCATGTGGA[C/T]GAGGCACACAAAGTT | 284434 |
rs373034774 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782336 | CCAGGCATGGTGGTG[A/T]GCACCTGAAGTCCCA | 284434 |
rs373037089 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16755534 | GCTGGGATTACAGGC[A/G]TGCACCACCATGCCT | 284434 |
rs373041986 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16769354 | GTAATCCCAGTTACT[C/T]GGGAGGCTGAGGCAG | 284434 |
rs373061251 | snp | A/C | 1.65701e-05 | 0.00287833 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807752 | CGAGGCCCGGAAAGC[A/C]ATCAACTGCATGTCC | 284434 |
rs373090685 | in-del | -/TTC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16730909 | TTTATTTTTCTTTCT[-/TTC]TTTTTTTTTTTTTTT | 284434 |
rs373115678 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16726673 | TGAACTCCTAACCTC[A/T]AGTGATCCACCCACC | 284434 |
rs373140451 | snp | A/C | 2.88913e-05 | 0.00380063 | intron-variant | NWD1 | GRCh38.p7 | 19:16794418 | TCCAGACTTGTAACC[A/C]TTAACCCGTGGAAGT | 284434 |
rs373147117 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16771958 | GCGCGCCACCATGCT[C/T]GGCTAATTTTTCTTA | 284434 |
rs373158027 | snp | A/G | 3.29587e-05 | 0.00405934 | missense | NWD1 | GRCh38.p7 | 19:16788991 | CTGCAGGAGAGGTGA[A/G]GTGTGTGAAAATATT | 284434 |
rs373199598 | in-del | -/ATGCCTATAGACCTAGC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16752528 | TGAGCATGGTGGTGC[-/ATGCCTATAGACCTAGC]TACTCCGGAGGCTGA | 284434 |
rs373209900 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787743 | CACATGCCTGTAATC[C/T]CAGCTACTCAGGAAG | 284434 |
rs373222022 | in-del | -/TTCCTT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782851 | GTTTCTTTTTCTTTC[-/TTCCTT]TTCCTTTTCCTTCTT | 284434 |
rs373258516 | snp | C/T | 8.40202e-05 | 0.00648098 | missense | NWD1 | GRCh38.p7 | 19:16749987 | TCTGTCCGCCATGCT[C/T]GGAGGGTTCCCTGGC | 284434 |
rs373274342 | snp | C/T | 1.68675e-05 | 0.00290405 | missense | NWD1 | GRCh38.p7 | 19:16750258 | GGCGGCTGAGGCTGG[C/T]GTTTGAGGAAGCCCG | 284434 |
rs373276532 | snp | C/T | 9.88598e-05 | 0.00702995 | intron-variant | NWD1 | GRCh38.p7 | 19:16812868 | GAGTCATTTTGCTTT[C/T]AGGGCAGGATTGAGC | 284434 |
rs373313438 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16733761 | GCCCGTCCTCTGACG[C/T]GGATGCTGTCAACAT | 284434 |
rs373324211 | snp | C/T | 3.3243e-05 | 0.00407681 | missense | NWD1 | GRCh38.p7 | 19:16765153 | CTGGTCCGTGAAGCC[C/T]TCCAGCTCTGCCGCC | 284434 |
rs373334984 | snp | G/T | 4.97368e-05 | 0.00498657 | stop-gained, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749432 | GCCTGCTACCTGAAG[G/T]AGCTGGGTGAGCAGT | 284434 |
rs373361485 | in-del | -/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16807188 | AAAAAAAAAAAAAAA[-/G]AAAGAAAGAAAATAT | 284434 |
rs373372872 | in-del | -/ATTTT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16760229 | AACATAAAATTCACC[-/ATTTT]ATTTTATTTTATTTT | 284434 |
rs373405532 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16810327 | CCTGTAATCCCGGCT[A/G]CCCGGGAGGCCGAGG | 284434 |
rs373406895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16803348 | CTTAGACAGGCCCCA[A/G]CTCCTAATACCATCC | 284434 |
rs373431741 | snp | C/T | 0.00478085 | 0.0486577 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718028 | AATTTTTTGTTATTG[C/T]TGTTGTTGTAGAGAT | 284434 |
rs373482038 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751539 | GGCATGGTGGCTTAC[A/G]CTTTTAATCGCAGCA | 284434 |
rs373489588 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16738947 | TATGTTGCCCAGGCT[A/G]GTTTTGAACTCCCGG | 284434 |
rs373497345 | snp | A/G | 1.73742e-05 | 0.00294734 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750352 | ACTCTGCACCCGCCT[A/G]GAGCAGACACACGGG | 284434 |
rs373604184 | snp | A/G | 3.45728e-05 | 0.00415755 | missense, intron-variant | NWD1 | GRCh38.p7 | 19:16749828 | TTCCAGGTGTGCCTG[A/G]CCTATGGGCTGCCCT | 284434 |
rs373629121 | in-del | -/TCT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16767166 | AGGGAAAGAGGTGCG[-/TCT]TTTTTTTTTTTTTTT | 284434 |
rs373636322 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16773939 | ATTCATCCATCCATC[C/T]ATCCATCCATCCATC | 284434 |
rs373662367 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16731027 | GGAGAGAGAATCTCT[C/T]GAGGCCAGGAACTCG | 284434 |
rs373782906 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16757706 | AGGCTCTCAACCTAG[C/T]GGTTCACCCATGACC | 284434 |
rs373800351 | snp | C/T | 0.000230791 | 0.0107397 | missense | NWD1 | GRCh38.p7 | 19:16763873 | ACGGTTGCAAACCTG[C/T]GGAAGCTGAAGGAGT | 284434 |
rs373811297 | snp | G/T | | | missense, upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749158 | TGAGTGGGAGATAGA[G/T]CGGAGCCTGCTGAGC | 284434 |
rs373828318 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16810609 | CCCATCTCTAGAAAA[A/C]AAAATTAGCCAGGTG | 284434 |
rs373829175 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16736845 | AGGGAAGTAGGTACC[A/G]TTTCTGCTTTCGTAC | 284434 |
rs373838164 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | NWD1 | GRCh38.p7 | 19:16763784 | TGCGTGGAGTGAATG[A/G]ATGGGTTTGTGTCCA | 284434 |
rs373858739 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16739734 | GTCATTAGGCAGCAC[C/T]GAGGCCGGGGACAGC | 284434 |
rs373869121 | snp | C/T | 8.38947e-05 | 0.00647613 | missense | NWD1 | GRCh38.p7 | 19:16750192 | GGAGGACGCTGAGCC[C/T]GGTGCACACAGATTT | 284434 |
rs373873680 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16810170 | AGGCTGGGCACCATG[A/G/T]CTCACACCTGTAATC | 284434 |
rs373890312 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750085 | GGACACCTTGCAGCG[A/G]GTGCTCCTGGACCCG | 284434 |
rs373914212 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732098 | GGCTCATGCCTGTAG[C/T]CCCAGCTACTCAGGA | 284434 |
rs373981805 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16736185 | CTTTTTCTTTCCTTC[C/T]TTCCTTCTTTCCTTC | 284434 |
rs373981941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16814705 | CCTTAAAAGCCCATC[C/T]TGGGCCAGTTCACAA | 284434 |
rs374012637 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16810617 | TAGAAAAAAAAATTA[G/T]CCAGGTGTGGAGGTG | 284434 |
rs374019741 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16810772 | TGTCTCTCGAGCAAA[A/T]CTAACTAATAAACAA | 284434 |
rs374029844 | snp | C/T | 0.000280892 | 0.0118477 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16773169 | GGCCAGACTCCATTT[C/T]TTCGCCACCTCACAT | 284434 |
rs374057081 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16731424 | CGATTCTCCTGCCTC[A/G]GCCTCCTGAGTAGCT | 284434 |
rs374085775 | in-del | -/TAT | 0.462363 | 0.131916 | intron-variant | NWD1 | GRCh38.p7 | 19:16742882 | TCTCACTATGTTGCC[-/TAT]TATTATTATTATTAT | 284434 |
rs374157106 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16728747 | CAGGAGATTGAGACC[A/C]TCCTGGCTAACACAG | 284434 |
rs374195694 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16771770 | TCCGTACATCCAAGC[A/C]CGCTGGCGAATGGGG | 284434 |
rs374207879 | snp | A/G | 1.66891e-05 | 0.00288864 | missense | NWD1 | GRCh38.p7 | 19:16750056 | TCAGCTTGCTCGGGG[A/G]CACTGGGGGTTTTGG | 284434 |
rs374216329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16781677 | TACTATTGTTTGAGG[A/G]CAAGGGTTATGTTTT | 284434 |
rs374284829 | in-del | -/TTTC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16761368 | TTCTTTCTTTCTTTC[-/TTTC]CTTCTTTCTCTTTTT | 284434 |
rs374296512 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16769648 | AACATCCAAGCTTGC[A/G]TGCCGGGGGCCCTGG | 284434 |
rs374332636 | in-del | -/GTTGCAGTGAGCCGAG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16784865 | ACCCGGGGGGCGGAG[-/GTTGCAGTGAGCCGAG]ATCGCGCCACTGCAC | 284434 |
rs374353773 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16734208 | AAGTGTGGACACGTC[C/T]TTGCTTTCAAAGCAA | 284434 |
rs374392647 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16808340 | GGATCACCTGAGATC[G/T]GGAGTTCAAGACCAG | 284434 |
rs374407485 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16784135 | ACTTGAACCTGGGAG[A/G]TGGAGGTTGCTGTGA | 284434 |
rs374420379 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16771315 | ATTAGCCGGGTGTGG[C/T]GGTGCATGCCTGTAA | 284434 |
rs374502216 | snp | A/G | 1.64784e-05 | 0.00287035 | missense | NWD1 | GRCh38.p7 | 19:16779351 | GCTGCAGGCATCACC[A/G]CCATGGCATGGGGTG | 284434 |
rs374522747 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16811384 | AGGTCAGGAGTTCGA[A/G]ACCAGCCTGACCAAC | 284434 |
rs374529462 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16757874 | CTGGCCAACATAGTG[A/C]AACCCCATCTCTACT | 284434 |
rs374530936 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16789676 | AAAACCTTTCAAATT[A/C]ATTGAGACTTCTTTT | 284434 |
rs374583971 | snp | C/T | 3.31862e-05 | 0.00407333 | synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749467 | GGTGAGGGCCAATCA[C/T]CAGGTCCTCACACGC | 284434 |
rs374594106 | in-del | -/TA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16775306 | AGATGTTGTAAAAAA[-/TA]AAATGGCCAAAATAT | 284434 |
rs374653249 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16719791 | TAACCACTAAGTCTG[G/T]GCTGAATGCCCGGCT | 284434 |
rs374676545 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16798906 | GCTGGGATTACAGGC[A/G/T]TGAGCCACCATGTCT | 284434 |
rs374678328 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751864 | GAAAGAAAAAAAAAG[A/G]AGGAAAGAAGAGATA | 284434 |
rs374684286 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16809416 | TTAAAAATCTAAAAT[A/G]AATACCAAAATTCCA | 284434 |
rs374691203 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16725091 | ATCTTGGCTCACTGC[A/G]ACCTCTCTGCCTCCC | 284434 |
rs374691740 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16807012 | ACGAAGCCAGACTCT[A/G]TCTAAAAAAAACAAA | 284434 |
rs374691800 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16734999 | GAACTCCTGGGTTCA[A/G]GCAATCCTCATGCTT | 284434 |
rs374700146 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16723180 | CTAGGACCGCAGACA[C/T]GAATCACCATGTCCA | 284434 |
rs374712988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16724334 | TGCTGCAGAGACAAG[C/T]GCCCTGAATGGCTCT | 284434 |
rs374823612 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16763313 | GTCTAAAACCTTCCA[C/T]AGCTCCCCAGTGCCC | 284434 |
rs374823996 | snp | A/G | 0.000281678 | 0.0118642 | missense | NWD1 | GRCh38.p7 | 19:16791593 | CAAGGAAAGCTTGTT[A/G]CCGGGTTTAGCAATG | 284434 |
rs374876983 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16811586 | GAGACTCTGTCTCAG[-/A]AAAAAAAAAAAAAAG | 284434 |
rs375040257 | snp | A/C | 3.31543e-05 | 0.00407137 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16765143 | TGAGGTTGGCCTGGT[A/C]CGTGAAGCCCTCCAG | 284434 |
rs375054081 | snp | A/C | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815774 | TGGAGTTCTGGTACC[A/C]GATGAAGGGGGAACG | 284434 |
rs375074899 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16780300 | AGCTGGGACTACAGG[C/T]GCCCGCCACCATGCC | 284434 |
rs375075463 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16739810 | TCAGCAGCCCCAGTG[A/T]CTCCAGAGCTCTGAG | 284434 |
rs375113440 | snp | C/T | 1.656e-05 | 0.00287745 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749349 | TCACTGACATGCACC[C/T]AGGGGTCCTCAAGAC | 284434 |
rs375121120 | in-del | -/AGG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16735864 | GGAAGGAAGGAAGGA[-/AGG]AGGAAGGAAGGAAGG | 284434 |
rs375193946 | in-del | A/CAAAC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16730347 | TAACAAAAAAACAAA[A/CAAAC]AAAAAACCCAAAATC | 284434 |
rs375200188 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817376 | GAGGCTGAGGCGGGT[A/G]GATCACTTGAGGCCA | 284434 |
rs375234481 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | NWD1 | GRCh38.p7 | 19:16728324 | GAGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTGC | 284434 |
rs375256551 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16741458 | GAAACCTCCCTCTCC[C/T]GGGTTCAAGCAATTC | 284434 |
rs375260890 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16735851 | AGGAAGGAAGGAAGG[-/A]AGGAAGGAAGGAAGG | 284434 |
rs375265853 | snp | C/T | 3.30857e-05 | 0.00406716 | intron-variant | NWD1 | GRCh38.p7 | 19:16779488 | TTGGGAAGTGGGCTT[C/T]GTGGTCAGCTTCCAT | 284434 |
rs375269352 | snp | A/C/T | 5.08991e-05 | 0.00504454 | intron-variant | NWD1 | GRCh38.p7 | 19:16763989 | CGAGCCTGGTGACTG[A/C/T]ACCACGCTCCAGTCT | 284434 |
rs375293723 | snp | A/G | 4.95683e-05 | 0.00497812 | missense | NWD1 | GRCh38.p7 | 19:16808108 | GGGACCTGCAGGCAC[A/G]CAAGTGGAAATTCGA | 284434 |
rs375297656 | snp | C/T | 2.66926e-05 | 0.00365316 | missense, intron-variant | NWD1 | GRCh38.p7 | 19:16794544 | GAAGATGAGTCCCTC[C/T]TCGCCGCAGGTAGCG | 284434 |
rs375298387 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16722829 | GCTGGGGATTAAGGT[C/T]AGCTATGCTGGTGGT | 284434 |
rs375318200 | in-del | -/TTTA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16747345 | GGCTGACATTTTCTT[-/TTTA]TTTATTTATTTATTT | 284434 |
rs375325443 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16738779 | AATGATATATAATAT[-/A]ATAATATATAATAAC | 284434 |
rs375351364 | snp | C/T | | | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718885 | GCTGGAGTGCAGTGG[C/T]GCGATCTCGGCTCAC | 284434 |
rs375367929 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16758813 | AGGAGTTGGAGACCA[A/G]CTTGACTAACATGGT | 284434 |
rs375374646 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16738741 | TAATCTATATATAAT[A/C]TATATATTATATATA | 284434 |
rs375377678 | snp | G/T | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748906 | CTGGACCAGCAAGCC[G/T]TGGCTTGTTGCAAAT | 284434 |
rs375383225 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16729481 | TCTGCCCCTCGATGT[A/T]AAGTAGATTTGTCCC | 284434 |
rs375413796 | in-del | -/GAAAAAGT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732670 | AAAAAAAAAAAAAAA[-/GAAAAAGT]GAAAAAGTGCAGTGG | 284434 |
rs375481125 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16767752 | GGGGATTACAATTCA[A/T]GATGAGATTTGGGTA | 284434 |
rs375494759 | snp | A/T | 4.97352e-05 | 0.00498649 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749433 | CCTGCTACCTGAAGG[A/T]GCTGGGTGAGCAGTT | 284434 |
rs375539059 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16807061 | GGCACAGTGGCAGGC[A/G]CCTGTAGTCTCAGCT | 284434 |
rs375547878 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16736990 | AGAGTAGAATGTTGA[A/C]GCCAGAAGGAATCTT | 284434 |
rs375565329 | snp | A/G | | | downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16818290 | AGAGAGTGAGACCAT[A/G]TCTCAGAAAAAAAAT | 284434 |
rs375572318 | in-del | -/C | | | frameshift-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749274 | GATGGTGGACCGGCT[-/C]CGCGGATGGCTGCCT | 284434 |
rs375588027 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16760113 | TGAGCCGTGACTGTA[C/T]CACTGCACTCCAGTC | 284434 |
rs375594148 | snp | C/T | 0.000318645 | 0.0126183 | intron-variant | NWD1 | GRCh38.p7 | 19:16763974 | CCCATCTCAGAGGAC[C/T]GAGCCTGGTGACTGC | 284434 |
rs375602441 | snp | A/G | 6.87853e-05 | 0.00586412 | missense, upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749160 | AGTGGGAGATAGAGC[A/G]GAGCCTGCTGAGCTC | 284434 |
rs375618349 | in-del | -/AACAAA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16762557 | AAACTCTGTCTCAAA[-/AACAAA]CAAACAAACAAAGTA | 284434 |
rs375635964 | snp | G/T | 5.476e-05 | 0.0052323 | intron-variant | NWD1 | GRCh38.p7 | 19:16794603 | GCTAATCAGGATCAG[G/T]TTGGAGAAGGGGGTG | 284434 |
rs375644805 | in-del | -/CAAGGCTAAGAATTTCCTTCCTTTT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16768314 | AATTTCCTTCCTTTT[-/CAAGGCTAAGAATTTCCTTCCTTTT]AAAGGCTTAATAATA | 284434 |
rs375674809 | snp | C/T | 0.00016608 | 0.00911111 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749499 | TCCGTGAGCTGGATA[C/T]GGCCGGACAGGAGTT | 284434 |
rs375683296 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | NWD1 | GRCh38.p7 | 19:16735388 | GTGCACGCCTGTAAT[A/C]CCAGCTACTCGGGAG | 284434 |
rs375702849 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16743236 | TTTCTTTAGAGACAG[G/T]GTCTCACTCTGTCCC | 284434 |
rs375706116 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16769596 | ACTCTCCTGGGAGAT[A/G]CTTGTCTCCATCCTT | 284434 |
rs375805813 | snp | C/T | | | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16721438 | GCGCTGAAGTGAATT[C/T]GGGTCCAAGGAGCCT | 284434 |
rs375842850 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16737437 | GGCTAGTATTTTTTT[-/T]GGAAATATGGGGTCT | 284434 |
rs375858553 | snp | A/G/T | 4.94298e-05 | 0.0049712 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807992 | TGCAACTTCCAAAGC[A/G/T]TTTCCCTTGGAGACC | 284434 |
rs375902245 | snp | A/G/T | 8.25929e-05 | 0.0064258 | intron-variant | NWD1 | GRCh38.p7 | 19:16759186 | CCAAATGCAGAAGAC[A/G/T]TGAGATGTGCCTCAA | 284434 |
rs375906944 | snp | C/T | 0.000148254 | 0.00860844 | missense | NWD1 | GRCh38.p7 | 19:16807930 | ATTCTGACGGACTAC[C/T]GCGTGGTCTACAGCA | 284434 |
rs375920280 | snp | A/C | 5.01886e-05 | 0.00500917 | intron-variant | NWD1 | GRCh38.p7 | 19:16791310 | ACTTGTAGTCTAGGT[A/C]TCCTGCCAAGATGCT | 284434 |
rs375923677 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16723617 | GTGCCTGGCCCCTTG[A/G]CTGATTTTAATTTAT | 284434 |
rs375958432 | snp | A/G | 1.65921e-05 | 0.00288024 | missense, utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16799949 | GTCGGGGCCCCCGTG[A/G]GCCTGCTGGCCCGCG | 284434 |
rs375959020 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16730019 | TCTTCACAAACTGCA[A/T]GTACTTTTTAAAACT | 284434 |
rs375960342 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16767210 | GGTGAGACAGAGTCT[C/T]GCTCTGTCGCCCAGG | 284434 |
rs375965910 | snp | A/G | 1.65712e-05 | 0.00287843 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749409 | TGAACCCCAAGAACA[A/G]GACTCACGCCTGCTA | 284434 |
rs376005618 | snp | A/C | 0.000199392 | 0.00998279 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749545 | AGAGATCCGCCACCA[A/C]CTTTGGCAGAGCTCG | 284434 |
rs376049867 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787901 | AATAATAATAATAAT[A/C]ATAATCATCATCATC | 284434 |
rs376053349 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16766329 | ATCAATTGAGCCTGG[A/G]AGGTCGAGGCTGCAG | 284434 |
rs376057700 | in-del | -/CAAAC | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16730346 | TAACAAAAAAACAAA[-/CAAAC]AAAAAAACCCAAAAT | 284434 |
rs376063372 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16794645 | CAGAGAGAAGTCCTA[A/G]GGCCAGAGGTTAGCA | 284434 |
rs376081430 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16773942 | CATCCATCCATCTAT[C/T]CATCCATCCATCCAT | 284434 |
rs376175973 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817470 | AGCCTGGTGTGGTGA[C/T]GTACACCTGTAATTC | 284434 |
rs376179114 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16801026 | GTCACACCTCTAATA[C/T]CAGCACTTTGGGAGG | 284434 |
rs376197344 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16736511 | TTTTAATCCAGACAT[A/C]CCCCTACAGGAAGAG | 284434 |
rs376233568 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732615 | TTTTTTTTTTTTTTT[C/T]AGATGAGGTCCAGTG | 284434 |
rs376247839 | in-del | -/TCCA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764493 | CCATCCATCCATCCA[-/TCCA]CTCATCCTTCTGTCT | 284434 |
rs376271090 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16811651 | AGAAATTGAGTCCTA[C/T]AATTGTTCCTTTCAG | 284434 |
rs376294522 | snp | A/G | 1.65132e-05 | 0.00287339 | missense | NWD1 | GRCh38.p7 | 19:16807780 | TCCCTGAGCAAGTGC[A/G]AGGACCGCCTGGCCA | 284434 |
rs376301633 | in-del | -/AAGCCAGACTGAGAACCCAACTTGATAGAGTTGCTGTGAG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16729125 | TGTTTCCTCCTCGAG[lengthTooLong]TGGCATACGATGTTA | 284434 |
rs376343624 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16781242 | ATCTCAAGGGTCCTC[C/T]CTTTGGGAGAGATGA | 284434 |
rs376425455 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NWD1 | GRCh38.p7 | 19:16765401 | TTCAGTGGTGCAATC[A/G]TAGCTCACTGTAGCC | 284434 |
rs376435260 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16725914 | AAGTAGCTGGGACAA[C/T]AGGCAGGCACCATCA | 284434 |
rs376448028 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16756123 | CTGGGCATGGTGGCT[C/T]ATGCTTTTAATTCCA | 284434 |
rs376481084 | snp | A/G | 4.97459e-05 | 0.00498703 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749438 | TACCTGAAGGAGCTG[A/G]GTGAGCAGTTTGTGG | 284434 |
rs376518628 | snp | G/T | 1.64754e-05 | 0.00287009 | utr-variant-3-prime, missense | NWD1 | GRCh38.p7 | 19:16815110 | CATTGCCCCCACCAG[G/T]CATGGTTATCTGATC | 284434 |
rs376565041 | in-del | -/A/AA | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16769471 | ATTAAAAAAAAAAAA[-/A/AA]GAGCCCAAATCTCAC | 284434 |
rs376566352 | snp | C/T | 0.000138679 | 0.00832589 | synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749749 | CAAGACAGTGACCGT[C/T]CTGCGGCTGCTGGGG | 284434 |
rs376583163 | snp | C/T | 8.38624e-05 | 0.00647489 | intron-variant | NWD1 | GRCh38.p7 | 19:16808165 | CTCCCCATGTTCATG[C/T]TAGACCCAGGCATTG | 284434 |
rs376596843 | snp | A/G | | | utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16724422 | GTCCTCCAGGAGGGC[A/G]ATGGAGGAGCCGGCA | 284434 |
rs376641733 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16810244 | GGGGTTCGAGACCAG[C/G]CTAGCCAACATGGTG | 284434 |
rs376659710 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782922 | TCCTTCTTTCCTTCC[-/T]TTCCTTCCTTCCTTC | 284434 |
rs376665471 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16734116 | TGAACTGCAAGCGTG[C/T]GGTTGCCAAGGAGAC | 284434 |
rs376668461 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16761260 | TTTGTTTATCTTCGT[C/T]TATGGATGGACACTT | 284434 |
rs376690404 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16746275 | TGACGTGGGAGGATT[A/G]CGTCAGCCTAGGAGG | 284434 |
rs376698524 | in-del | -/TTTTTT | 0.198944 | 0.244731 | intron-variant | NWD1 | GRCh38.p7 | 19:16809560 | TTCTTTTTCTTTTTC[-/TTTTTT]TTTTTTTGAGATGGA | 284434 |
rs376702966 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16720616 | GCTGGAGTGCAGTGG[C/T]GTGATCTCAGTTACT | 284434 |
rs376717883 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16735833 | GAAGGAAGGAAAGAA[A/G]GAAGGAAGGAAGGAA | 284434 |
rs376731145 | snp | C/G/T | 4.94697e-05 | 0.00497321 | missense | NWD1 | GRCh38.p7 | 19:16759232 | CCCTTCAGACACGGT[C/G/T]TCTCGGAGGCGGAGC | 284434 |
rs376756589 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16736255 | TCTTTCTTTTGACAG[A/C]GCCTGGCTCTGCTGT | 284434 |
rs376800039 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16731812 | TGAGTTTTAAAATTC[A/G]CAGTGATTTTTAAAC | 284434 |
rs376806286 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16809759 | AGATGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 284434 |
rs376841816 | snp | C/T | 3.38977e-05 | 0.00411676 | missense, intron-variant | NWD1 | GRCh38.p7 | 19:16749889 | CCAGGGTGGTCCAGT[C/T]TTTCCATACCCTCCT | 284434 |
rs376899915 | snp | C/T | 0.00140706 | 0.0264868 | synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744468 | GATTCCCTCGCGGAT[C/T]GATGAGAAGGAGTGG | 284434 |
rs376901172 | snp | G/T | 0.000307571 | 0.0123972 | intron-variant | NWD1 | GRCh38.p7 | 19:16763997 | GTGACTGCACCACGC[G/T]CCAGTCTTCTAGAGC | 284434 |
rs376901559 | snp | C/G | 0.000235885 | 0.0108576 | intron-variant | NWD1 | GRCh38.p7 | 19:16807579 | TCTCATTTTTCTTCC[C/G]TGGCAGGCGAGGAAC | 284434 |
rs376902807 | snp | C/T | 8.23866e-05 | 0.00641767 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807857 | CCCCTGCCCGGTCAT[C/T]GATGGGCCAAGATAC | 284434 |
rs376921925 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16813055 | AGAACTCCCTCCCTT[A/G]AGTTTTCATTAGGGC | 284434 |
rs376924320 | snp | A/G | | | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718888 | GGAGTGCAGTGGTGC[A/G]ATCTCGGCTCACTGC | 284434 |
rs376972770 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | NWD1 | GRCh38.p7 | 19:16763801 | TGGGTTTGTGTCCAA[A/G]CTGCAGTCTCCCTTC | 284434 |
rs377005112 | snp | C/G | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815599 | AGAGCTTCTCTTTCC[C/G]AACAGTCCTAGCCTC | 284434 |
rs377014055 | snp | A/C/G | 1.65616e-05 | 0.00287759 | synonymous-codon, missense | NWD1 | GRCh38.p7 | 19:16791586 | CCAGAAGCAAGGAAA[A/C/G]CTTGTTACCGGGTTT | 284434 |
rs377129066 | snp | G/T | 3.2975e-05 | 0.00406035 | missense, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800059 | GGTGCCTGCACCATT[G/T]CTGGACCGCACCGGC | 284434 |
rs377139098 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16736070 | TTCTGGTGAAGAACC[C/T]CATCCAGGGTACCCC | 284434 |
rs377141345 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16731988 | TTGGGAGGCAAAGGC[A/G]GGCAGATCGCTTGAG | 284434 |
rs377158506 | snp | A/G | 3.29522e-05 | 0.00405894 | missense | NWD1 | GRCh38.p7 | 19:16789012 | TGAAAATATTTGCCA[A/G]AGGGACCCTCGCCAA | 284434 |
rs377186225 | snp | C/T | 0.00019883 | 0.00996873 | synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749386 | CCTGCCGTGGAGCCG[C/T]GACTTGGTGAACCCC | 284434 |
rs377206904 | snp | A/G | 3.36202e-05 | 0.00409988 | intron-variant | NWD1 | GRCh38.p7 | 19:16797725 | ACCCCAGTTCCTGCC[A/G]TTTCAGGCTTTGGAA | 284434 |
rs377278485 | snp | G/T | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748850 | TAATAAGAAGAAGAA[G/T]AAGAGTAATGGCTTA | 284434 |
rs377284795 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16722244 | ATGGAGGCTGCAGTG[A/C]GCCACAATAGTGCCA | 284434 |
rs377341838 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16800505 | CTCTGCACTCCGGCC[G/T]GGGCGACAGAGTGAG | 284434 |
rs377346009 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16755889 | CAAACTGGGAGTTAG[A/G]GGAACCAGCTGTCTC | 284434 |
rs377353431 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16731452 | GCTGGGACTACAGGC[A/G]TGCGCCACCACGCCC | 284434 |
rs377363971 | in-del | -/TTTTTTG | | | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718681 | ACCACGCCCAGCTAA[-/TTTTTTG]TTTTTTGTTTTTTGT | 284434 |
rs377377022 | snp | A/G | 0.000149421 | 0.00864223 | intron-variant | NWD1 | GRCh38.p7 | 19:16731304 | GTCACTCCGGGCTCC[A/G]TGCTTTTTTTATTTT | 284434 |
rs377387235 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | NWD1 | GRCh38.p7 | 19:16794452 | TGACAGGCATCCCTG[G/T]TTCTGCACAGGTTTC | 284434 |
rs377438799 | snp | A/C/T | 0.000148899 | 0.00862723 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16762084 | CTGGAGCCAGGGTAC[A/C/T]AAGAAGCTCATCACT | 284434 |
rs377472991 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16759856 | AAAATTAGCCAGACG[C/T]GGTGGCACGTGCCTG | 284434 |
rs377513422 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16743364 | TACAGATGCACACCC[C/T]CACACCCTGATAATT | 284434 |
rs377542902 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16722711 | TTGGAATGGGATAAG[A/G]GTGTCTTTGTTTACC | 284434 |
rs377584244 | snp | A/G | 1.6727e-05 | 0.00289193 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750028 | CTGCCCCCCGAGGGT[A/G]CACCTCATCCTCTCA | 284434 |
rs377642593 | snp | A/C/T | 3.29957e-05 | 0.00406162 | missense | NWD1 | GRCh38.p7 | 19:16779459 | CACATGCTAACTGGA[A/C/T]ACACAGGTGAGACTT | 284434 |
rs377667652 | snp | A/G | 1.66167e-05 | 0.00288237 | intron-variant | NWD1 | GRCh38.p7 | 19:16773082 | GGCAGGGAGGGTAGA[A/G]GGGGCTCAATCCAGG | 284434 |
rs377676951 | snp | A/G | 4.94629e-05 | 0.00497283 | intron-variant | NWD1 | GRCh38.p7 | 19:16812887 | GCAGGATTGAGCTTC[A/G]ATCTGGAGAGAAAAG | 284434 |
rs377707846 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16730958 | AGATGAGGCTTTAGC[C/T]GCAGGCCAGGCGCAG | 284434 |
rs377718201 | snp | C/T | 3.34046e-05 | 0.00408671 | missense | NWD1 | GRCh38.p7 | 19:16750051 | TCCTCTCAGCTTGCT[C/T]GGGGGCACTGGGGGT | 284434 |
rs377724731 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16781961 | TAGCTGGGCGTGATG[A/G]TGGGTGCCTGTAGTC | 284434 |
rs377735797 | snp | A/G | 0.000115313 | 0.0075923 | missense | NWD1 | GRCh38.p7 | 19:16807931 | TTCTGACGGACTACC[A/G]CGTGGTCTACAGCAT | 284434 |
rs377756498 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16736605 | CTGTCATGCCACCTC[C/T]CTGACAAACTTGTGT | 284434 |
rs386388643 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16769465 | AATTCCATTAAAAAA[-/A]AAAAAAGAGCCCAAA | 284434 |
rs386807351 | multinucleotide-polymorphism | CA/TG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16720844 | AGGCGTGAGCCACCG[CA/TG]CCTGGCCGAGACTTT | 284434 |
rs386807352 | multinucleotide-polymorphism | AT/GC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16728899 | CAGCGAGCCGAGATC[AT/GC]GCCACTGCACTCCAG | 284434 |
rs386807354 | in-del | ATT/GC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16738628 | TATTTTCTGAGATCT[ATT/GC]TTCTGAGACCTAAAG | 284434 |
rs386807355 | multinucleotide-polymorphism | CGTGGGAGGATTGCGTCAGCCTAGGAGGCGGAGA/GGTGGGAGGATTGCGTCAGCCTAGGAGGCGGAGG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16746263 | TACTCAGGAGAGTGA[lengthTooLong]TTGCAGTGAACCAAG | 284434 |
rs386807356 | multinucleotide-polymorphism | GC/TT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16759758 | TTAGCACTTTGGGAG[GC/TT]TGAGGTGGCGGATCA | 284434 |
rs386807357 | multinucleotide-polymorphism | CTT/TTC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16761348 | ACCTGTTCCCTTTCT[CTT/TTC]TCTTTCTTTCTTTCT | 284434 |
rs386807358 | in-del | ATCCATCCATCCATCCATCCA/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764365 | ACCCATCTTCTGTCC[ATCCATCCATCCATCCATCCA/G]TCCATCCATCCATCC | 284434 |
rs386807359 | multinucleotide-polymorphism | CA/TG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16778915 | GCTGACTTCTGGGGC[CA/TG]AATCTTTCTCTGGGA | 284434 |
rs386807360 | in-del | CT/TTCC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782864 | TTCTTCCTTTTCCTT[CT/TTCC]TTCTTTCTTTCTTTC | 284434 |
rs386807361 | multinucleotide-polymorphism | AG/CA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16799663 | AGGCATGCACCACCA[AG/CA]CCTGGCTAATTTTTT | 284434 |
rs386807362 | multinucleotide-polymorphism | AGCCTGGCTAATT/CACCCAACTAATA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16799663 | AGGCATGCACCACCA[AGCCTGGCTAATT/CACCCAACTAATA]TTTTGTATTTTTATT | 284434 |
rs386807363 | multinucleotide-polymorphism | CAA/TGG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16799667 | ATGCACCACCAAGCC[CAA/TGG]CTAATTTTTTGTATT | 284434 |
rs397780041 | in-del | -/T | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16793594 | GGTTGTTTTTTTTTT[-/T]GAGACTGAGTCTTGC | 284434 |
rs397796367 | in-del | -/AA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16775309 | TGTTGTAAAAAAAAA[-/AA]TGGCCAAAATATCAG | 284434 |
rs397859573 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16728282 | GCTGGGTCACTGCTC[-/T]TTTTTTTTTTTTTTT | 284434 |
rs397859685 | in-del | -/TTCT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782882 | TCTTTCTTTCTTTCT[-/TTCT]CTTTCTTTTTCCATC | 284434 |
rs397964268 | in-del | -/AGAAA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16738013 | AGAAAAGAAAAGAAA[-/AGAAA]TTCTAGAGCAGAGGC | 284434 |
rs397973642 | in-del | -/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16755730 | TTAGTAGAGATGGGG[-/G]TCTCACTATGTTGCC | 284434 |
rs398034094 | in-del | -/A | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16728964 | AAAAAAAAAAAAAAA[-/A]TAAGTAATTGCAGCT | 284434 |
rs398034095 | in-del | -/T | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16766603 | ACCATTTTTTTTTTT[-/T]GAGACAGGATCTCGC | 284434 |
rs398034097 | in-del | -/A | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16793071 | AAAATAAAAAAAAAA[-/A]GAAAAGAAAAGAAGA | 284434 |
rs398059599 | in-del | -/AAA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16722120 | CCTGTCTCTTGAAAA[-/AAA]CAACAACAACAACAA | 284434 |
rs398059600 | in-del | -/TTTA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16747382 | TTATTTATTTATTTA[-/TTTA]ATTTTTTTTGAGACA | 284434 |
rs398079761 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16769470 | CCATTAAAAAAAAAA[-/A]AGAGCCCAAATCTCA | 284434 |
rs527259733 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16746506 | AGTGAAACTCTGTCT[C/G]TACTAAAATTACAAA | 284434 |
rs527337404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16774646 | CCCATCCTTTCATCC[A/G]TCCATCCACCCACCC | 284434 |
rs527393387 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16757510 | TTTGGCAGATGAGGA[A/G]ACTGAGGCAAAGAGA | 284434 |
rs527397943 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16750567 | TCAAGTGATCCTCAC[A/G]CCTCACCTGCTGAGT | 284434 |
rs527475181 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | NWD1 | GRCh38.p7 | 19:16734652 | TGCAATCACAGCTCA[A/C]TGCAGCTTTCTGGGC | 284434 |
rs527508301 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16780593 | GGGAAATAGGCTAAA[C/T]AGGCTTTCTGCCTTC | 284434 |
rs527539413 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16742227 | TAAAAATATAAAAAT[A/T]AGCCAGGCGTGGTGG | 284434 |
rs527566334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16783516 | ATATATACCTGTAAT[C/T]CCAGCTACTCGGGAG | 284434 |
rs527624275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16789994 | AAGTGCTGGGATTAC[A/G]GGCCTGAGCCATCAT | 284434 |
rs527626330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16782750 | CCTGTAGTCCCAGCT[A/G]CAAGGAGGAGGATGC | 284434 |
rs527633033 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16795846 | CACTGCTTCTATTGC[A/G]TGGAGCAGCTTCCCT | 284434 |
rs527646932 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16774735 | TCATCCATTCATTCA[C/T]CCTTCAACCCTTTCT | 284434 |
rs527649177 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16768126 | CAGCCTCCAGAGTAG[C/G]TGGGATTACAGGTGT | 284434 |
rs527670769 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16740474 | CTGAGTAGCTGGGAT[A/T]ACAGGTGCCCACTAC | 284434 |
rs527677097 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16728715 | TTTGGGAGGCCGAGG[C/T]GGGCGAATCACGAGG | 284434 |
rs527680560 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16812587 | GGCAGGAGAATCGCT[A/T]GAACCTGGGAGGTGG | 284434 |
rs527696514 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16725960 | TTTTTTTTTTGTTTG[-/T]TTTTTTTTTGCTTTT | 284434 |
rs527831615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16787639 | CCGAGGCGGGTGGAT[C/T]ACCTGAGGTCAGGAG | 284434 |
rs527849728 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16763285 | ATCCAATCTGATTAT[G/T]ATTATGCCTCTTGTC | 284434 |
rs527915241 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16762880 | GCCTCTGCCTCCCAG[C/G]TTCAAGCGATTCTCC | 284434 |
rs527939152 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16772293 | TCGCTTGAGCCCAGG[A/T]GTTTGAGGCTGCAGT | 284434 |
rs528003554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16727668 | TCATCAGTTCCACAG[C/T]CTCAGGTAAGGTGCA | 284434 |
rs528035162 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16772229 | AACTAACGAGGCGTG[A/G]TGACGTGCATCTGCA | 284434 |
rs528069067 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817152 | TAAAAATACAAAAAT[C/G]AGCCAGGCATGGTGG | 284434 |
rs528075446 | snp | A/G | | | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16717879 | AAGAGACAGGGTTTT[A/G]CTCTGTTGCCCAGGC | 284434 |
rs528090864 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16809745 | TATTTTTTTGGTAGA[G/T]ATGGGGTTTCACCGT | 284434 |
rs528104530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16771514 | ACTGGAATTTAAGGC[A/G]ACTGGAAAGAAAAAT | 284434 |
rs528237169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16784787 | TACAAAAATTAGCCA[A/G]GTGTGATGGCACACA | 284434 |
rs528245754 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16754542 | TCTATCCATCATCTC[A/G]ATCTTCCATCCTTCC | 284434 |
rs528245875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16760944 | CTCATAATGTTGCAC[C/T]CCTCACCTCTGTCTA | 284434 |
rs528278448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16805060 | TTTATTTTATTTTTG[C/T]TGTTGTTCTTTTGTT | 284434 |
rs528279974 | snp | C/G/T | 3.38604e-05 | 0.00411449 | intron-variant | NWD1 | GRCh38.p7 | 19:16797933 | CCTCCACCTCGGGAA[C/G/T]AGACACTGATTCTTT | 284434 |
rs528289315 | in-del | -/AAAAAAAAAA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16759022 | AAAAAAAAAAAAAAA[-/AAAAAAAAAA]TCGGAAAAGGTCTTC | 284434 |
rs528301680 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16811644 | AGAAAAAAGAAATTG[A/G]GTCCTACAATTGTTC | 284434 |
rs528306101 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16760485 | GGCTGGTCTCGAGCT[C/G]CTGGGCTCAAGAGAC | 284434 |
rs528332104 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16762358 | CTGGAGTGCAATGGC[A/G]TGATCTCAGCTCACT | 284434 |
rs528343404 | snp | A/C | 0.195526 | 0.243993 | intron-variant | NWD1 | GRCh38.p7 | 19:16787876 | AAATAGTAATAATAA[A/C]AATAATAATAATAAT | 284434 |
rs528354951 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16726438 | TTAAACTGTTTTCTT[C/T]CTTTTTTTCTTTTTT | 284434 |
rs528374751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16765635 | GAGCCATGGCGCCTG[A/G]CCTAGAATTTTAAAT | 284434 |
rs528385711 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16814324 | TAGGTTTGAGGCTGA[C/G]CTTCCTGATTTCAGT | 284434 |
rs528393361 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16785855 | CTTTTGTGTCCATTG[A/C/G]CTCTTTTTTTTAAAT | 284434 |
rs528416297 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16723111 | CAGTGGTGGCTCACT[G/T]CAGCCTCAACCTCCT | 284434 |
rs528417379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16725229 | GGCTGATCCTAGACT[C/T]CTAGGCTCAAATGAT | 284434 |
rs528450272 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16802572 | TTTTGTATTAAGAAG[A/C]AGCAGCCTGGGGCCC | 284434 |
rs528467053 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16759077 | CCTAACCGTGCTTGG[G/T]ACCTTGTGGGCGCTG | 284434 |
rs528470027 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718542 | TTCTTTGAGATGGAG[A/G]CTTGCTCTGTCGCCC | 284434 |
rs528479532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16724469 | GGATGCCAAGGTATA[C/T]GCGTGTTCTCTCTGC | 284434 |
rs528531486 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16758541 | CTCAGCCTCCCAAAG[G/T]GCAGGGATTACAGGT | 284434 |
rs528549185 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16723897 | GACGGGGTTTCACCA[C/T]GTTGGCCGCGCTGGT | 284434 |
rs528586857 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815460 | CAGATTATGGCTTCA[A/G]ACCTTGTCTCTTCTC | 284434 |
rs528612584 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16729405 | TCACGGTTCCCTCTT[C/G]TCCTTCTTATTCTGA | 284434 |
rs528613035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16806689 | GCACTCCAGCCCGGG[C/T]AACAGAGTGAGACTC | 284434 |
rs528640490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16743061 | GGGATTACACCTGCA[C/T]GCCACCATGCCTGGC | 284434 |
rs528676304 | in-del | -/ACTAA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16760171 | ACTAAACTAAACTAG[-/ACTAA]ACTAAACTAAACTAA | 284434 |
rs528723797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16747754 | CGCAGGCAACCATCA[A/G]TCTGCTTTCTGTCTC | 284434 |
rs528725858 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16781616 | GCGAGACCCTATCTC[-/A]AAAAAAAAAGCAAGA | 284434 |
rs528750766 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16790900 | ATGTGAGGCCTGGCC[A/C]ACCTCTCCTTTTTTT | 284434 |
rs528811876 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16796898 | GATGAGTGATTACTG[G/T]CTGGGTACGGTGGCT | 284434 |
rs528848337 | snp | C/T | 4.98873e-05 | 0.00499411 | synonymous-codon, utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16799945 | AGGCGTCGGGGCCCC[C/T]GTGAGCCTGCTGGCC | 284434 |
rs528886575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16722062 | AGGCTGCAGTGAGCT[A/G]TGATCATGTCACTGC | 284434 |
rs528907569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16799595 | CATTGCAAACTCCAC[C/T]TCCCGGGTTCAAGCG | 284434 |
rs528938624 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16769274 | TGAGACCAGCCTGGC[C/T]AACAGGGTGAAACCC | 284434 |
rs528950011 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16721471 | TGGGACCCAGGAAAA[C/T]GAGAGAAGGAACAGA | 284434 |
rs528951042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16727601 | CGCCGGCGGCTTCTG[C/T]GGGGTGAAGCCGGCC | 284434 |
rs528966709 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16805972 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 284434 |
rs528985213 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16761746 | TTTATGTGTAAATTT[G/T]GGAGGAGCTCAAATG | 284434 |
rs528995188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16812402 | GGTCAGGCACGTTGG[C/T]TCACACCTGTAATCC | 284434 |
rs529021124 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16727494 | CTGCCTGGCTGCTGG[C/T]GTGAGGTCTCTGAGC | 284434 |
rs529036309 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16726323 | ACTGTGTTGCCCTGG[C/T]TGGCCTTGAACTGCT | 284434 |
rs529090879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16788406 | AAACCCGTCTCCACT[A/G]AAAATAGAAAAAATT | 284434 |
rs529124723 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16745705 | AGATCATGCCACTGC[A/G]CTCCAGCCGGGGTTA | 284434 |
rs529139112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16787731 | CAGGCGCGGTGGCAC[A/G]TGCCTGTAATCCCAG | 284434 |
rs529166500 | snp | A/G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16722352 | GGAGTGCAATGGTGC[A/G/T]ATCTCAGCTCACTGC | 284434 |
rs529181065 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16730560 | CTCTACAAAAAATTT[A/T]AAAAAATATATATGG | 284434 |
rs529201209 | snp | A/C | 8.80844e-05 | 0.00663584 | missense, intron-variant | NWD1 | GRCh38.p7 | 19:16794472 | GCACAGGTTTCCTCC[A/C]AAGGGGACAGATTGC | 284434 |
rs529246893 | snp | A/G | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744464 | GTCTGATTCCCTCGC[A/G]GATCGATGAGAAGGA | 284434 |
rs529255982 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16786180 | ATTTTTATTATTTTT[A/G]CTTTTTTTTTTAGAG | 284434 |
rs529288303 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16743062 | GGATTACACCTGCAC[A/G]CCACCATGCCTGGCT | 284434 |
rs529375132 | in-del | -/CT | 0.00636936 | 0.0560724 | intron-variant | NWD1 | GRCh38.p7 | 19:16721371 | AGGCAAGGTCAAAGA[-/CT]CTTATCCTCCTGCGA | 284434 |
rs529418010 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16792314 | GGGAGGCTGAGGGGG[C/G]GTGGATCATTTGAGG | 284434 |
rs529419644 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16767352 | AGGTGTGGTGGCTCA[C/T]GCCTATAATCCCAGC | 284434 |
rs529436050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16798482 | CGGGCGTCATGGCAT[A/G]TGCCTGTAGTCCTAG | 284434 |
rs529446452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16720743 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 284434 |
rs529460061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16773592 | CAAGGGATTGGTGCC[C/T]ATCTGACAGTTTCAG | 284434 |
rs529499484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16732382 | GTCATTTAACTGTCT[A/G]TTGTTGTTGCTGCTG | 284434 |
rs529500682 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16818410 | AAGACAAATAATATT[C/T]TGTTATCTTTTTTTT | 284434 |
rs529522642 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16780280 | CCTGCCTCAGCCTCC[A/C]GAGTAGCTGGGACTA | 284434 |
rs529607339 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744985 | CCTGGCACAGGGGCC[A/G]TATTAGTCTGTTCTC | 284434 |
rs529629285 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16737981 | AAAAGAAAAGAAAAG[A/C]AAAGAAAAGAAAAGA | 284434 |
rs529633115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16786691 | AGCTGGGATTACAGG[C/T]GCACACCACCACACC | 284434 |
rs529639400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16763408 | TCCCTACTCTCATTT[C/T]CCACCCGCATCCCCT | 284434 |
rs529692487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16783578 | GGTGGAGGTTGCAGT[A/G]AGCCGAGATCGCGCC | 284434 |
rs529711853 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16771831 | CGCGATCACGAGTCC[-/T]TTTTTTTTTTTTTTT | 284434 |
rs529732982 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16797195 | AAAAAAAAAAAAAAA[A/C/T]TGATGAGTGATTACA | 284434 |
rs529762699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16746566 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 284434 |
rs529795257 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16722213 | CTGAGGTGGGAGGAT[C/T]ACTTGAGGACAGGAG | 284434 |
rs529839686 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16783725 | AATTTAAGACCCTGT[C/T]TCTTAAAACAAATAA | 284434 |
rs529841524 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16810437 | GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 284434 |
rs529842836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16796077 | TGGCTGAGTCTGGGC[A/G]TTTTTATAGGCACAG | 284434 |
rs529851877 | snp | A/G | 0.021333 | 0.101051 | intron-variant | NWD1 | GRCh38.p7 | 19:16764373 | TCTGTCCATCCATCC[A/G]TCCATCCATCCATCC | 284434 |
rs529912369 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16730050 | ATTTATGGGCCGGGC[A/G]CAGTGGCTCACGCCT | 284434 |
rs529913640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16776895 | TGCAGTGAGCTGTGA[C/T]TGTGGCACTGCACTC | 284434 |
rs529982937 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16784225 | AAAAAAAAAAAAGAA[A/T]AATTAAGTATACAGG | 284434 |
rs529995416 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16762941 | GGTGTGTGCCACTGC[A/G]CCTGGCTAATTTTTG | 284434 |
rs530026594 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16734110 | CACAAATGAACTGCA[A/G]GCGTGCGGTTGCCAA | 284434 |
rs530028471 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16728015 | GCAGTGAGCCAAGAT[C/G]GCGCCATAGCACTCC | 284434 |
rs530041330 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16807459 | GATCGTGCTATTGCA[C/G]TACAGCCTGGGCAAC | 284434 |
rs530057607 | snp | A/G | 3.31741e-05 | 0.00407259 | synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749455 | TGAGCAGTTTGTGGT[A/G]AGGGCCAATCACCAG | 284434 |
rs530075747 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16813242 | CAAGTCACTAGTAGT[G/T]GGGGGCTGGTTACAT | 284434 |
rs530089235 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16733544 | AAAAAAAATCAAGTG[G/T]CTCTTTGGGTAAAAA | 284434 |
rs530103218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16813973 | TCTGGACAACATAGC[A/G]AGACTCTGTCTCTAC | 284434 |
rs530158158 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16797680 | GATGGAAGGAATGAC[C/G]CTCAATCTCCTCTGG | 284434 |
rs530193974 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16757001 | TGTCTCCCATCACCC[C/T]CAGATGGGACTGTCT | 284434 |
rs530196956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16758197 | AACTTTGAAAGATGG[C/T]TCATGCAACCAAGAA | 284434 |
rs530273582 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16801235 | AGTGAGCCGAGATCA[C/T]GCCATTGCACTCCAG | 284434 |
rs530298228 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16774880 | ATCCACACACTTAGC[A/C]ATTCATCAACTTTCT | 284434 |
rs530355320 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16728673 | TTGCAGGCCGGGTGC[A/G]GTGGCTCACACCTGT | 284434 |
rs530386101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16723230 | TTGAGATAGGGTCTC[A/G]CTCTGTTGTCCAGGC | 284434 |
rs530401181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16810744 | CTCCACCCTGGATGA[C/T]GATACAAGATTCTGT | 284434 |
rs530410830 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16763372 | GATATTCAGTGCCTT[C/T]GTGATCTGCTGCTTA | 284434 |
rs530421899 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16725915 | AGTAGCTGGGACAAC[A/T]GGCAGGCACCATCAT | 284434 |
rs530434388 | snp | C/T | 3.32e-05 | 0.00407417 | missense | NWD1 | GRCh38.p7 | 19:16807744 | CCCCCTCCCGAGGCC[C/T]GGAAAGCAATCAACT | 284434 |
rs530446734 | in-del | -/AATG | 0.000119126 | 0.00771677 | utr-variant-3-prime, frameshift-variant | NWD1 | GRCh38.p7 | 19:16815290 | CAGGGAAATGAAACC[-/AATG]AAATCAAACAAATGC | 284434 |
rs530451726 | in-del | -/ATT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16741535 | CATGCCCGGCTAATT[-/ATT]TTTATATTTTTAATA | 284434 |
rs530478391 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16760683 | GCAACCTCTGCCTCC[C/G]AGGTTTCAGCGATTC | 284434 |
rs530483947 | snp | A/C | 0.000281849 | 0.0118678 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16731277 | ACGGCTTGATGTTTG[A/C]GGTAACTGGAAGTCA | 284434 |
rs530537635 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16773072 | AGACTCAATTGGCAG[A/G]GAGGGTAGAGGGGGC | 284434 |
rs530542976 | in-del | -/A | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16812297 | TGGGTCAGACCTGTT[-/A]AAAAAAAAACAAAAA | 284434 |
rs530544966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16737345 | CATGGCTCACTACAG[C/T]CTTGAACTCCTGGGC | 284434 |
rs530546708 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16765710 | CATCCTGTTGCCCTG[G/T]ACTTTTCTTTAGAAA | 284434 |
rs530589530 | snp | G/T | 8.98271e-05 | 0.00670115 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815355 | ATAAAAAAACCCTGT[G/T]GGGGTATGGGGCTCC | 284434 |
rs530601709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16772303 | CCAGGAGTTTGAGGC[C/T]GCAGTGAGCTGCGAT | 284434 |
rs530602872 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16791148 | CTGAGGCAGGAGGAT[C/T]GCTTGAGCCCAGGAG | 284434 |
rs530662365 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16779227 | GGGCAAGGGACCAAA[G/T]CTCTCTGTGCCTCAG | 284434 |
rs530665008 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16788349 | TCAGGTGGGTGGATC[A/G]CTTGAGGCCAGGAGT | 284434 |
rs530697459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16755645 | CTGCCACCTTGGCCT[C/T]CCAAAGTGCTAGGAT | 284434 |
rs530706562 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16761097 | TCTGGGCATTTCAGA[C/T]CAACGAAATCTCACA | 284434 |
rs530736359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16792825 | GAGGTTGCAGTGAGC[C/T]GAGATCATGCCATTG | 284434 |
rs530738173 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16799515 | TTTATTTTTATTTTT[A/T]TTTTTTTTGAGACGG | 284434 |
rs530752122 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16805258 | GAGATGGGGTTTCAC[C/T]GTGTTGGCCAGGCTA | 284434 |
rs530800036 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16798652 | TTTTTTGAGACCAAG[A/T]CTCACTCAGTCGCCC | 284434 |
rs530815808 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16719625 | ACCTTTCTGCATCTT[A/G]TTTTCTTCATCTGTG | 284434 |
rs530820630 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751870 | AAAAAAAAGAAGGAA[A/G]GAAGAGATAAAGGAA | 284434 |
rs530860435 | in-del | -/T/TT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16780158 | CAAAGGCAAGGTTTC[-/T/TT]TTTTTTTTTTTTTTT | 284434 |
rs530868740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16720325 | AAATTAAAATAAGGC[A/G]ATGGCATTGGGAGTG | 284434 |
rs530878086 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16795624 | GTTTCATCATGTTGG[A/C]CAGGCTGGTCTTGAA | 284434 |
rs530887513 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16803397 | TGACATAGGAATTTG[G/T]TGGGGGGGTGGGGAC | 284434 |
rs530911013 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782210 | ACCTGTAATCCCAGC[A/G]CTTTGAAGATGGGAG | 284434 |
rs530949330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16802943 | CAAGAGTCAGACTCT[A/G]TCTCAAAAAAAAAAA | 284434 |
rs530956525 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16752889 | CTGTAGTCCCAGCTA[A/C]TCGGGAGGCTGAGGC | 284434 |
rs530972883 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16808482 | TTGAAATTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 284434 |
rs530995579 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16784817 | ACCTGTAGTCCCAGC[C/T]ACTCAGGAGGCTGAG | 284434 |
rs530996055 | snp | A/G | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16743980 | GAGCCACCGCGCCTG[A/G]CCGATATACATTTAT | 284434 |
rs531005037 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718995 | ACGCCCAGCTAATTT[C/T]TTGTTTTGTTTTGTT | 284434 |
rs531014335 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16785542 | ATAAAATAAAATAAA[C/T]AAACAAAATTTAAAA | 284434 |
rs531016156 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16737774 | GTCAGGAGATTGAGA[A/C]CAGCCTGGGCAACAT | 284434 |
rs531025584 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16759117 | TGATCCCAGGTGATG[C/T]GCTGGACACCGCGCG | 284434 |
rs531126426 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16739949 | GTCTGTGGTTGGCTT[A/G]TGTCTTAGTCTATTT | 284434 |
rs531183371 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16743673 | TTATTTATTTATTTA[A/T]TAGTTTGTTTATTTA | 284434 |
rs531200223 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16784865 | ACCCGGGGGGCGGAG[C/G]TTGCAGTGAGCCGAG | 284434 |
rs531217447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16794896 | AAACGATCCTCCCAC[A/G]TCAGCTTCCTGAATA | 284434 |
rs531241094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748266 | TGGGATTACAGGCAT[A/G]AGACCCCATGTCCAG | 284434 |
rs531291046 | in-del | -/T | 0.149665 | 0.228982 | intron-variant | NWD1 | GRCh38.p7 | 19:16780159 | CAAAGGCAAGGTTTC[-/T]TTTTTTTTTTTTTTG | 284434 |
rs531291501 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16742680 | GAGATAAATTGTATA[C/T]ATATTTTGAGACGGA | 284434 |
rs531299411 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16756640 | TCTATACATCTGCCT[A/G]TCTATCATGCTACCA | 284434 |
rs531304336 | snp | C/T | 0.000500175 | 0.0158062 | intron-variant | NWD1 | GRCh38.p7 | 19:16750463 | TTATGTTTTCTTTTT[C/T]TATTTTTAGAGATGG | 284434 |
rs531318756 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16772054 | TCCAATATATCCCTC[C/T]TCTGATCCTACTTTT | 284434 |
rs531341804 | snp | C/T | 0.000396845 | 0.0140807 | synonymous-codon, utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16799966 | CCTGCTGGCCCGCGG[C/T]GGGGCTTTGGTGGCA | 284434 |
rs531367180 | snp | C/G | 6.6538e-05 | 0.00576755 | missense | NWD1 | GRCh38.p7 | 19:16750122 | TACTGGGAGGTGAAG[C/G]CCCTTTCCGGAAACC | 284434 |
rs531382209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16797280 | TGAATCCACCTTCCC[C/T]GTCCTGGATCCCTTC | 284434 |
rs531382907 | in-del | -/GT | 0.000810768 | 0.0201178 | intron-variant | NWD1 | GRCh38.p7 | 19:16773105 | AATCCAGGCAACTTA[-/GT]CTACATCCCTTTGTT | 284434 |
rs531429518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16762774 | TGCCTTTTCTTTTTC[C/T]CTCCCTCGCTTCCTT | 284434 |
rs531450183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16740881 | TTGTGCAGGGGGGCC[A/G]GGTGCAGTGGCTTAC | 284434 |
rs531473864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16807385 | GTAATCCCAGCTACT[C/T]GGGAGGCTGCGGCAG | 284434 |
rs531491304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16781982 | GCCTGTAGTCCCAGC[C/T]ACTCGGGAGGCTGAG | 284434 |
rs531535601 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16729032 | GCACATTGGGAGGCC[A/G]AGGTGGGAGAATTGG | 284434 |
rs531546736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16788463 | AATCCCAGCTACATG[A/G]GAGGCTGAGGCACGA | 284434 |
rs531557010 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16782559 | CATATTCAAATTTTT[A/T]AAAAATTTAAAGGGG | 284434 |
rs531610843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16780346 | ATTTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 284434 |
rs531618773 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16779261 | TCTTATCTGTGAAGT[A/G]GGGGGCTCATTAGAG | 284434 |
rs531684261 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16752388 | ATGCTGGGTGCAGTA[C/G]CTCACTCCTGTAATG | 284434 |
rs531697989 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16786722 | CAGCTAACTTTCGTA[G/T]TTTTAGTAGAGACGG | 284434 |
rs531723124 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16723885 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 284434 |
rs531841943 | snp | A/G | 0.000304275 | 0.0123307 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744556 | TACTTCCAGAGGGAC[A/G]AGAATGCGTTTCCTC | 284434 |
rs531890183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16793615 | TGAGTCTTGCTCTGT[C/T]GCCCAGACTGGAATG | 284434 |
rs531906094 | snp | C/T | | | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744945 | TCTCCTCGCTGGCTC[C/T]TTCTTCTTGTCTCCC | 284434 |
rs531936113 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16727624 | AGCCGGCCCCCTCCC[A/C]GCACCTCCACCCAGC | 284434 |
rs531973839 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16778275 | CCAATATATCTTGGC[C/G]CTTCTCTCTCTGCAG | 284434 |
rs531991331 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | NWD1 | GRCh38.p7 | 19:16801140 | CAAAATTAGCTGGGC[A/G]TGGTGGTGCATGCCT | 284434 |
rs532008468 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16812570 | GCTACTTGGGAGGCT[A/G]AGGCAGGAGAATCGC | 284434 |
rs532072407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16780861 | ACAGGGTCTCACTAT[A/G]TTGCTGAGGCTGGTC | 284434 |
rs532085014 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16747720 | ACCCATTAAACACTC[C/T]CCATCTCCCCTCTCC | 284434 |
rs532085072 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | NWD1 | GRCh38.p7 | 19:16742390 | AAAAAAATAAAATAA[A/T]TAATAAATAAATAAA | 284434 |
rs532116154 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16735403 | CCCAGCTACTCGGGA[G/T]GCTGAGGCAGGAGAA | 284434 |
rs532121501 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16818249 | GTAGTTAGCTATGAT[C/T]GCACCACTGCACTCT | 284434 |
rs532136843 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815802 | ACGGATGAATGTGAG[A/G]TACAGCAAATCACTG | 284434 |
rs532157053 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NWD1 | GRCh38.p7 | 19:16777235 | AAGGGAAGGGGAGGG[A/G]AGGGAAGGGGAGGGA | 284434 |
rs532157735 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16783618 | CAGCCTGGGCAAAAA[C/G]AGCAAAACTCCATCT | 284434 |
rs532194171 | in-del | -/C | 0.00517822 | 0.0506191 | intron-variant | NWD1 | GRCh38.p7 | 19:16805815 | TTGAAAATCAGGATT[-/C]CTTTCTCCTATTATT | 284434 |
rs532221372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16784359 | TAACACAGCCAGACC[C/T]GTATCTCTAAAAATA | 284434 |
rs532258837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16782444 | GTATTCCATCCTGGG[C/T]GACAGAGTGAGACCT | 284434 |
rs532267893 | snp | A/G | 0.155325 | 0.23138 | intron-variant | NWD1 | GRCh38.p7 | 19:16764385 | TCCATCCATCCATCC[A/G]TCCATCCATCCATCC | 284434 |
rs532304008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16759729 | AAAAAAAATAAGAAA[A/G]TTAGCTAGGTGTGTT | 284434 |
rs532325204 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NWD1 | GRCh38.p7 | 19:16736331 | GCCTTGTGGGCTCAA[C/T]TGATCCTCCTACCTC | 284434 |
rs532346838 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16725133 | ATTCCCATGCCTCAG[C/T]CTCTCGAATAGCTGG | 284434 |
rs532370822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16723355 | AGGTGTGCACCACCA[C/T]ATCTGGCTAATTTTT | 284434 |
rs532371072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16729347 | AGAATCCATAGATCC[A/G]GGAACCCACAAGGCC | 284434 |
rs532380418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16801544 | GAGTTTGAGACCAGA[C/T]GTCTCTACATAAAAG | 284434 |
rs532407797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16724628 | TCAGGTGGGAGGATC[A/G]TTTGTTGGCAGGAGC | 284434 |
rs532431474 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NWD1 | GRCh38.p7 | 19:16728726 | GAGGCGGGCGAATCA[C/T]GAGGTCAGGAGATTG | 284434 |
rs532437398 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16814866 | TTATCATTCCCATTG[C/T]GCAGATAAAGGAAGA | 284434 |
rs532455097 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816306 | GACTTTTATGCAAAA[A/G]TGTTCTGACTTTTAA | 284434 |
rs532462810 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16803378 | CTATGGGGAGTGAGG[A/G]TTTTGACATAGGAAT | 284434 |
rs532519715 | snp | C/G | 1.66241e-05 | 0.00288302 | intron-variant | NWD1 | GRCh38.p7 | 19:16763793 | TGAATGAATGGGTTT[C/G]TGTCCAAGCTGCAGT | 284434 |
rs532543299 | in-del | -/TCCATCCATCCATCCATCATCTCT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754706 | CCATCATCTCTAGCA[-/TCCATCCATCCATCCATCATCTCT]ATCTTCCTTCCATCC | 284434 |
rs532582689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16763414 | CTCTCATTTCCCACC[C/T]GCATCCCCTAACCTG | 284434 |
rs532605649 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718817 | ACTGGCGTGAGCCAC[A/C]ATGCCTGGGTGACTT | 284434 |
rs532631437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16757172 | ACCCCTACCCTGGTC[C/T]GCGGGAAAAAAATTG | 284434 |
rs532658446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16734144 | GACCTTGGTACGTCC[A/G]GTGCTGGCCAAACTA | 284434 |
rs532699881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16723840 | AGCTGGGATTACAGA[C/T]GTGCACCGTCATGCC | 284434 |
rs532704486 | in-del | -/A/AA | 0.624019 | 0.109895 | intron-variant | NWD1 | GRCh38.p7 | 19:16769460 | AGCAAAATTCCATTA[-/A/AA]AAAAAAAAAAAGAGC | 284434 |
rs532707038 | snp | A/G | | | missense | NWD1 | GRCh38.p7 | 19:16765060 | TGGATTTCCTGCCGG[A/G]GCATCTCTGGGGGCA | 284434 |
rs532747087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16805879 | CTTTCTTTTCTTCTT[C/T]TTTTTTTGAGAGGGA | 284434 |
rs532764788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16790103 | ACATCAATCATAACC[C/T]TGTGATTTCATAGTT | 284434 |
rs532811238 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718464 | AGGCATGAGCCACCG[C/T]GCCTGACCAAGTATC | 284434 |
rs532824145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16726670 | GTTTGAACTCCTAAC[C/T]TCAAGTGATCCACCC | 284434 |
rs532869037 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16810812 | AATTAACATGTGAAC[A/T]GTACTATTAATTAAA | 284434 |
rs532880622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16801929 | AGGAGGCAGAAACAG[A/G]AAGATTGCTTGAGGC | 284434 |
rs532940168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16727016 | GAGGGGGTGGGAAGG[A/G]CAGAATGGGGTGGGA | 284434 |
rs532988841 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16767318 | GGGAGCAACTGCCTT[A/T]TAAAACCATCGGACG | 284434 |
rs532999871 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16767368 | GCCTATAATCCCAGC[A/C]CTTTGGGAGGCCGAG | 284434 |
rs533084831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16755796 | TCCCACCTTGGCCTC[C/T]CAAAGTGCTGGGATT | 284434 |
rs533091630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, splice-acceptor-variant | NWD1 | GRCh38.p7 | 19:16721396 | CCTGCGATCATCAGC[A/G]GGCAGTAACCAAGGG | 284434 |
rs533107078 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16799558 | GTTGCCCAGGCTTGC[A/G]TGCAATGGCACGATC | 284434 |
rs533163601 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16792267 | ATAGACTGGCTGGGC[A/G]CTGTGTCTCACTCCT | 284434 |
rs533171068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16786790 | CTCCTGAGCTCAGGC[A/G]ATCTGCCCGCCTCAG | 284434 |
rs533198024 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16756324 | GGATATCACAAAGGT[C/T]TTCATCCTTGTCATC | 284434 |
rs533224464 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | NWD1 | GRCh38.p7 | 19:16799831 | TGAAGCGTATTTCTG[A/T]ACTATAGTTGTCCAC | 284434 |
rs533354678 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817790 | AGGGCTTACCCAATG[C/T]AGAAATAAAGTAGAT | 284434 |
rs533372152 | snp | C/T | | | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16719097 | GCCTGCCTTGGCCTC[C/T]CAAAGTGCTGGGATT | 284434 |
rs533386312 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16779785 | GGGACTACAAGCACA[G/T]ACCACTATACCCAGC | 284434 |
rs533401758 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16785106 | GGGGAGTGACTGCTG[A/G]TGGGGACAGGGTCTC | 284434 |
rs533409142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748433 | GGCGTGATAGTAACT[C/T]CATGTTTCACTTTTT | 284434 |
rs533439908 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16740192 | TAGTCCTAGCTGCTC[C/T]GGAGGCTGAGATGGG | 284434 |
rs533439927 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16720185 | AATTTACTGAGCACC[C/T]ACTATGTGCCAGGCA | 284434 |
rs533474280 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16753777 | TTAGCCTGAGAGACC[C/G]TATCCATTCATCCAT | 284434 |
rs533483802 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16770216 | TTGAGGGAGGGACCA[G/T]GTGGAGATAATCGAA | 284434 |
rs533490205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16785646 | TACACTTATATATAC[A/G]TATTTTAATCTATAT | 284434 |
rs533491901 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16792633 | GATGCAGTGAGCCAA[C/G]ATTGCACCACTGCAC | 284434 |
rs533500888 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16797643 | ATGAACCACCACATC[C/T]GGCCTCCAAAACACC | 284434 |
rs533506209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16812967 | AGCTGCATCCCTTAG[C/T]TTTTAGGAAGGTGTC | 284434 |
rs533561922 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16720975 | CCTGCCTCAGGCTTC[C/T]GAGTAGCTGGGATTA | 284434 |
rs533566930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16742362 | CCTGGGCGACAGAGG[A/G]AGATTCCATCTCAAA | 284434 |
rs533592552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16746179 | GGCAACATGGCAAAA[C/T]CTCACCTTTATTTAA | 284434 |
rs533610441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16788550 | TTCCAGCCTGGGTGA[C/T]AGAGAGAGTCCGTCA | 284434 |
rs533629929 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16737413 | ACTACAGGTGTGTGC[C/T]GCCACAGTTGGCTAG | 284434 |
rs533670822 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16787995 | GCACTGTGGGAGGCC[A/G]AGGTGGGTAGATCAC | 284434 |
rs533685291 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16744080 | CATTTACTTATATAT[C/T]GAATTGGAGAAAGAA | 284434 |
rs533688030 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16730924 | TTCTTTTTTTTTTTT[C/T]TTTTGAGATGGTGGC | 284434 |
rs533727635 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16722860 | CAATCATGTCTACGT[G/T]ACCAACTCCCAATAA | 284434 |
rs533733383 | snp | A/C | 0.000399281 | 0.0141238 | missense | NWD1 | GRCh38.p7 | 19:16807874 | ATGGGCCAAGATACA[A/C]CTTTTACACTCAGCT | 284434 |
rs533736686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16728773 | CACAGTGAAACCCTG[C/T]CTCTACTAAAAATAC | 284434 |
rs533746400 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16740980 | CCTGGCCAACATGGC[A/G]AAACCCTGTCTCTAC | 284434 |
rs533755915 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16730342 | CAAACTAACAAAAAA[A/C]CAAAAAAAAAACCCA | 284434 |
rs533771052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16769689 | GCCTCCCCCAGCCCT[C/T]CTGTGGCAACTTTGG | 284434 |
rs533773529 | snp | A/G | 3.59712e-05 | 0.00424079 | missense | NWD1 | GRCh38.p7 | 19:16807616 | CCCTGGACACCTCCA[A/G]TGAGATCAGGTGTCT | 284434 |
rs533809774 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16740145 | CTAAAAAAAAAAAAA[C/G]AACAGTTAGCTGGGG | 284434 |
rs533860277 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16755497 | AGGTTCAAATGATTC[G/T]CATGTCTCAGCCTCT | 284434 |
rs533876074 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16745890 | CCACTGCACTCCAGC[A/C/G]TGGGTGACAGAGTGA | 284434 |
rs533987283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16726851 | CCTGGTCTCCACCCA[C/T]GTGATGCCAGTAGCA | 284434 |
rs534001097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16763076 | TGTAATTACAGGTGG[A/G]ATTACCACACCTAGC | 284434 |
rs534049548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16728321 | ATGGAGTCTCACTCT[A/G]TCGCCCAGGCTGGAG | 284434 |
rs534052143 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16731862 | TTTGCACCGAGCCCC[A/G]TAGATTCTGTAGTTG | 284434 |
rs534080341 | snp | A/C/G | 0.000679942 | 0.018426 | missense | NWD1 | GRCh38.p7 | 19:16773285 | TCCTCCAGCCCCCGG[A/C/G]AGGACCCCTCCGGGC | 284434 |
rs534107837 | in-del | -/T | 0.0267878 | 0.112589 | intron-variant | NWD1 | GRCh38.p7 | 19:16737567 | TGGTCTAGTTTTAAG[-/T]TTTTTTTTTTTTTTG | 284434 |
rs534118414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16813533 | CCAGGCTGGAGTGCA[A/G]TGGTGCAATCTCAGC | 284434 |
rs534144451 | in-del | -/TAA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16788283 | TAATAATAATAATAA[-/TAA]AAGGCCAGGCATGGT | 284434 |
rs534156745 | snp | A/G | 5.1202e-05 | 0.00505948 | missense, intron-variant | NWD1 | GRCh38.p7 | 19:16749865 | CTGCCCAGGTTCTGG[A/G]CGCCCACACCAGGGT | 284434 |
rs534186276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16727240 | CGCTCTGAGGACGAG[A/G]AGCTGGGAAGAGGAC | 284434 |
rs534218279 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16805542 | TCACTCTTTTGCCCA[C/G]ACTGGTCTTGAACTC | 284434 |
rs534218864 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NWD1 | GRCh38.p7 | 19:16762335 | AGAGTCTTACTCTGT[C/T]GCCCAGGCTGGAGTG | 284434 |
rs534220148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16812019 | AGATTCCATCAAAAA[C/T]AAAAACAAAAAACAG | 284434 |
rs534241775 | snp | A/G | 0.139225 | 0.224118 | intron-variant | NWD1 | GRCh38.p7 | 19:16799668 | TGCACCACCAAGCCT[A/G]GCTAATTTTTTGTAT | 284434 |
rs534253214 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16732556 | GTCCCAAAACAGTAG[A/G]AGCCCCTAATGCTGT | 284434 |
rs534272877 | snp | C/T | 0.000164875 | 0.00907801 | missense | NWD1 | GRCh38.p7 | 19:16759236 | TCAGACACGGTCTCT[C/T]GGAGGCGGAGCTGAA | 284434 |
rs534285390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16773886 | CCACCCTTCCATTCA[C/T]CTATCCATCCATCCA | 284434 |
rs534291330 | snp | A/C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16792920 | CATGGTGGTGCATAC[A/C/T]TGTACTCCCAGCTAC | 284434 |
rs534337636 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16764605 | TGGTCATCCATCCAT[C/G]CATCCACCCATCATT | 284434 |
rs534349013 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16780404 | CTTGTGATCCACCCA[C/T]CTCGTCCTCCCAAAG | 284434 |
rs534367849 | snp | A/G | 0.000216705 | 0.010407 | missense | NWD1 | GRCh38.p7 | 19:16750149 | AACCAAGGCCAGCAG[A/G]TGATCCAACTCCTGC | 284434 |
rs534376953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16730195 | GGTGTGGTGGTGCAC[A/G]CCTGTAATCCCAGCT | 284434 |
rs534405424 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16808989 | CTTGGAGGGCTGAGG[C/T]GGAAGGATTGATTGA | 284434 |
rs534444547 | snp | G/T | 0.00676609 | 0.0577691 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815936 | TACAGATGAGGAAAC[G/T]GAGCCTTGCGGAAGT | 284434 |
rs534453798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16747022 | CTGTCTAGTTCCAAG[A/G]TATTTTCTTTTTCTT | 284434 |
rs534460001 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16722126 | TCTTGAAAAAAACAA[A/C]AACAACAACAACAAC | 284434 |
rs534503108 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16806790 | GAGGCCGAGGCGGGC[A/G]GATCACTTGAGGTCA | 284434 |
rs534507964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16791816 | CCTCTCGGGTTCAAG[C/T]GATTCTCACTGCCTC | 284434 |
rs534522340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16721696 | GAGGGGGTCTGACCC[A/G]CACTCGCTCCCTGAC | 284434 |
rs534533995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16753935 | TCCATCATCTCAATC[C/T]TCCATCCTTCCATCC | 284434 |
rs534559409 | snp | A/G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16758511 | TTGAGCTCTGGCCTC[A/G/T]AGCAGTCCTCCTGCC | 284434 |
rs534593690 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16753021 | GTGCAAATAACAACT[C/G]GGGCATGTTCCAGAA | 284434 |
rs534639673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16809202 | AACTCTCCCGCCTCG[A/G]CCTCCCAAGTAGCTG | 284434 |
rs534700212 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16796232 | GGCCATCACCTGAGA[A/T]CAGAAGTTCAGATCA | 284434 |
rs534731133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16808649 | GGGACCCCACTGTCA[C/T]GAGGCTGTAGTACAG | 284434 |
rs534732841 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16729698 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 284434 |
rs534738178 | in-del | -/A/AA/AAAAAA/AAAAAAA/AAAAAAT | 0.331317 | 0.275459 | intron-variant | NWD1 | GRCh38.p7 | 19:16775300 | AGGCTCAGATGTTGT[-/A/AA/AAAAAA/AAAAAAA/AAAAAAT]AAAAAAAAATGGCCA | 284434 |
rs534750795 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | NWD1 | GRCh38.p7 | 19:16777635 | GAAGTGGAGGGGAAG[G/T]GGGAGGGAAGGGGAA | 284434 |
rs534751327 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732238 | AAAAAAAAAAAAGGC[A/G]GATGGAGGGGTTACA | 284434 |
rs534755715 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16770531 | ACACACAGAGACCAC[A/C]AATTTTGAGCCCCAC | 284434 |
rs534758994 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16717949 | ACTTTCTGGGCTCAA[A/G]TAATCCTCCCACCTC | 284434 |
rs534777742 | in-del | -/A/AA/AAA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16735963 | GCAGGACTCCAACTC[-/A/AA/AAA]AAAAAAAAAAAAAAA | 284434 |
rs534797256 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16778508 | TCTTTTTTTTTTTTT[-/T]GTTGTTGTTGTTGTT | 284434 |
rs534802154 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16801598 | GCTCACATCTGTAGT[A/C]CAAGCTACTTGGGAG | 284434 |
rs534816872 | in-del | -/AAT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787877 | AATAGTAATAATAAC[-/AAT]AATAATAATAATAAT | 284434 |
rs534834276 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16723407 | TTTCACCATGTTGCC[C/T]AGGCTGGTCTTGAAC | 284434 |
rs534855564 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748087 | CTCCCGGGTTCAAGT[G/T]ATTCTCCTGTCTTAG | 284434 |
rs534864404 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16735077 | CTAAATGTTTATAAA[G/T]AAACTTCTGAATTTG | 284434 |
rs534869965 | snp | C/T | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16791281 | AGAAGGCATCTTGCA[C/T]TTGACTCCGGGAAAC | 284434 |
rs534873265 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16738662 | GTCCCAACATTATAA[C/T]GAAAGACTGTAACAA | 284434 |
rs534897099 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16792734 | GCCCAAAAATTAGCC[A/G]GGTGTGGTGGTGGGT | 284434 |
rs534908397 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790465 | ACACTTGAAATTCGG[A/G]GGGTAGGGGGTAAGG | 284434 |
rs534936672 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16761076 | TGTCTCTGTGGATTT[A/G]CCTGTTCTGGGCATT | 284434 |
rs534980504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16746639 | GATCGCACCACTGCA[C/T]TCCAGCCTGGCAGCA | 284434 |
rs534988350 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16742029 | GGTTGCAGTGAGCTG[A/C]GATTGTACCACTGCA | 284434 |
rs535009633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16789666 | TTGATGATGTAAAAC[C/T]TTTCAAATTCATTGA | 284434 |
rs535035408 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16790160 | CGTGGGTGATAGCTT[A/G]CTAATTGATGCCAGG | 284434 |
rs535043530 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NWD1 | GRCh38.p7 | 19:16751588 | GGTGGATCACTTGAA[A/G]TCAGGAATTTGAGAC | 284434 |
rs535080534 | snp | A/G | 0.000822165 | 0.0202585 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744655 | GTCCTACGCTCTGGA[A/G]CCCAGGAGGCCCGGA | 284434 |
rs535087297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16767544 | TGCTTGAACACGGGC[A/G]GCAGAGGTTGCAGTG | 284434 |
rs535122661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16757791 | AGGTGCAGTGGCTCA[C/T]GCCTAATCCCAACAC | 284434 |
rs535157256 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16793135 | TTCTGAACCTCATGA[A/C]CTGTGGTCTTCATGA | 284434 |
rs535169891 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16745342 | ATTTGGGTGAAGACA[C/T]AGCCAAACCATATCA | 284434 |
rs535181124 | snp | G/T | 1.64928e-05 | 0.00287161 | utr-variant-3-prime, stop-gained | NWD1 | GRCh38.p7 | 19:16815225 | TCCAGGCAGAGAGAG[G/T]AGCTAGTTGCAGCTG | 284434 |
rs535189759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16798892 | TGGCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 284434 |
rs535210300 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16793345 | CTCAAGACGTCCTCT[A/C]GCCTCAGCCTCCTGA | 284434 |
rs535227776 | in-del | -/G | 0.00933717 | 0.0676861 | frameshift-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744600 | CAGGCACCAGGTACT[-/G]GGGGAGGCCTGTGAA | 284434 |
rs535236137 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16776621 | CCAAGGTCACACAAT[A/G]AGTGCATAAGAAAAA | 284434 |
rs535273695 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16724596 | CTCACACCTGTAATA[G/T]CAGCACTTTGGGAGG | 284434 |
rs535312086 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16747042 | TCTTTTTCTTTCTTT[-/C]TTTTTTTTTTTTGAG | 284434 |
rs535368875 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16805008 | AGACTTTAAAATTTT[A/T]AAAAATATTTATTTA | 284434 |
rs535372407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16738480 | AAGCTGAGGCAGGAT[A/G]ATCATTTGAAACTGG | 284434 |
rs535403809 | snp | C/T | 3.45161e-05 | 0.00415414 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749661 | CCCCCCTGGTACTCT[C/T]TGGGCCCCCAGGCAT | 284434 |
rs535441290 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817494 | GTAATTCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 284434 |
rs535524206 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16785783 | AAACAAATATATACA[C/T]AAATATATAAATATA | 284434 |
rs535524446 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16778818 | GTGCTGGGTGGCATG[A/G]GCCACCGTGCCCGGC | 284434 |
rs535565692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16720943 | GCAACCTCTGCTTCC[C/T]GGGTTCAAGCGATTC | 284434 |
rs535575082 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16793542 | AATTTGTTTTTTACC[-/T]TTTTTTTTTTAACTG | 284434 |
rs535579128 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16743776 | AAACCTCCCTCTCCC[C/G]GGTTCAAGCAATTCT | 284434 |
rs535583718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16785047 | ACAGAGACAGGAGAG[A/G]CAAGAGGCAGATTAG | 284434 |
rs535630019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16798274 | TGAAGTTCTCTTTTT[C/T]TCCCCCTCCTTCTTA | 284434 |
rs535651338 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16773934 | CATCCATTCATCCAT[A/C]CATCTATCCATCCAT | 284434 |
rs535663377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16720543 | TGCCCCCTAGGGGAC[A/G]TTGCAATGTCTAGGG | 284434 |
rs535710056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16780436 | GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCCC | 284434 |
rs535749720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16765989 | ACCACTGCACTCCAG[C/T]CTGGGCAACAGAGTG | 284434 |
rs535811885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16772593 | GCAGGTTGCAGTGAG[C/T]CAAGATCGCACCATT | 284434 |
rs535820295 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16731636 | TTGAGACAGAGTCTC[A/G]CTCTGCCACCCAGGC | 284434 |
rs535874294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16769185 | ACCATCAGATGGCCA[A/G]GTGTGGTGGCTCATG | 284434 |
rs535875831 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16759854 | CAAAAATTAGCCAGA[C/T]GCGGTGGCACGTGCC | 284434 |
rs535881979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16744127 | GGGACAGTGGCTCAC[A/G]ACAGTAATCCCAGCA | 284434 |
rs535890918 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16736773 | TCTTGGGAGGAATGG[C/G]TTAGCTCTTACTCCT | 284434 |
rs535892080 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816864 | TGCAAATGTTAGTGT[C/G]AAATTTCATTTAAAA | 284434 |
rs535915567 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16741733 | GCTACGTACGACCCA[G/T]GTTTTACCCTTTCTT | 284434 |
rs535930237 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16782866 | CTTCCTTTTCCTTCT[C/T]TCTTTCTTTCTTTCT | 284434 |
rs536009087 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16754871 | TATCTTCCATCCATC[C/T]ATCCATTCATCCACC | 284434 |
rs536009208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16761309 | TGCTGTTGTGAACAT[A/G]CATGTGTAAGGTTTT | 284434 |
rs536037112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16795579 | CTGCTACCACGTCCC[A/G]CTAATTTTTGTATTT | 284434 |
rs536038639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16726690 | GTGATCCACCCACCT[C/T]GGCCTCCCAAAGTGC | 284434 |
rs536071927 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16760820 | GTCTCAAACTCCTGA[A/C]CTCAGGTGATCTGCC | 284434 |
rs536079638 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16772086 | TTGAAAAGGTTGAGT[C/T]TGAGCACAGTGGCTC | 284434 |
rs536086726 | snp | A/G | | | intron-variant, missense | NWD1 | GRCh38.p7 | 19:16812841 | ATACTTGTTTGGAGT[A/G]TGCTGGATGGTGAGT | 284434 |
rs536105844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16801639 | TAGGATCACTTGAGC[C/T]CAGGAGGCAGAAGTT | 284434 |
rs536120770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16808339 | CGGATCACCTGAGAT[C/T]GGGAGTTCAAGACCA | 284434 |
rs536170402 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16731407 | TGCCTCCCGGGTTCA[A/C]GCGATTCTCCTGCCT | 284434 |
rs536176613 | snp | C/T | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816825 | TTTTCCAAACCAGTT[C/T]TCCAAGGCAGGTTTT | 284434 |
rs536189571 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16769782 | CTATGTCTCCCCGAT[A/C]CTTGCCTCTGAATTT | 284434 |
rs536234780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16814372 | TTACACTGTCTCCTA[C/T]AGAAAAGGCGCTCAT | 284434 |
rs536236252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16728347 | TGGAGTGCAGTGGTG[C/T]GATCTGGACTCACTA | 284434 |
rs536305657 | snp | A/G | 0.000512486 | 0.0159994 | missense | NWD1 | GRCh38.p7 | 19:16797750 | TTGGAAGATCGGTGC[A/G]GATATTCTTGGCGGA | 284434 |
rs536327337 | snp | C/T | 1.64912e-05 | 0.00287147 | missense | NWD1 | GRCh38.p7 | 19:16762020 | GCTACCTGTCAGGAT[C/T]CGAGAGAGCCAAGAG | 284434 |
rs536357917 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16741089 | CACTTGAATCTGGGA[A/G]GCAGAGGTTGCAGTG | 284434 |
rs536367182 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16796396 | AAACCCAGGAGGTGA[A/G]GATTGCAGTGAGCCA | 284434 |
rs536393370 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16753556 | CAGGATAGTTCTCCA[C/T]GCCCCCCATCCCCCC | 284434 |
rs536405015 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16775755 | CTCACTGCACCTCTG[C/T]TTCCCAGATTCAAGC | 284434 |
rs536410385 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16751718 | AGGCAGGAGAATCAC[G/T]TGAACCCGGGAGGCA | 284434 |
rs536481041 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16745926 | TGTCTCTAAATAAAT[A/T]AATTAATTAATTAAA | 284434 |
rs536484005 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16750668 | GAGATAGGGGTCTGG[C/T]TCTGTCACCCAGGCT | 284434 |
rs536486366 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16802152 | AGCCGGACGTGGTGG[C/T]GGGCACCTGTAATCC | 284434 |
rs536506013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16723426 | CTGGTCTTGAACCCT[C/T]GGACTCCCAAAGTGC | 284434 |
rs536510994 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16776908 | GATTGTGGCACTGCA[A/C]TCCAGCCTGGGTGAT | 284434 |
rs536526246 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16763600 | CCTTCAGGAAACATT[A/C]CCTATTCCTCCCAGA | 284434 |
rs536537642 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16757173 | CCCCTACCCTGGTCC[A/G]CGGGAAAAAAATTGT | 284434 |
rs536572124 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16775566 | TTCATTTTAAGGGCA[C/T]GACCTGGAAGCAGAA | 284434 |
rs536573949 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16804412 | CCAGCCTGGGCAACA[C/T]AGTGAGACCCCACCT | 284434 |
rs536604571 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16754013 | CTTTTATCCATCATC[A/T]CTATCTTCCATCTAT | 284434 |
rs536623553 | snp | C/T | 0.00050776 | 0.0159255 | missense, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800142 | ACAAAAACAAAGTCA[C/T]TATTTGGGACTTGGC | 284434 |
rs536641901 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NWD1 | GRCh38.p7 | 19:16722170 | AGGCATGGTGGTGTG[C/T]GCCTGTTAATCCCAG | 284434 |
rs536682163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16806966 | AGGTTACAGTGAGCC[A/G]AGATTGTGCCACTGC | 284434 |
rs536699213 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16761469 | GCAACCTCCACCTGG[C/G]AGGAGTGATTCTCCT | 284434 |
rs536726278 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16765285 | GAGCTGGATTTTCAT[A/C]AATTCTCATACCTTT | 284434 |
rs536744916 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16806410 | TGATGTGGGAATACA[A/G]AAGTCTGGCCCCCTT | 284434 |
rs536750226 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16809835 | GTGCTGGGATTACAG[G/T]CATGAGCCACCGTGC | 284434 |
rs536769667 | snp | A/G | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16724810 | TAATTCTCCTGCCTC[A/G]GCCTCCCAAGTAGCT | 284434 |
rs536773797 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16783777 | AAAGGAAAATATTTG[A/G]GAAAAAAATAGTTAA | 284434 |
rs536774966 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16812663 | AACAAGAGTGAAACT[C/G]CATCTCAAAAACAAA | 284434 |
rs536817989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16744144 | CAGTAATCCCAGCAC[C/T]TTGTGAGGCTGAGAT | 284434 |
rs536827497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16746264 | ACTCAGGAGAGTGAC[A/G]TGGGAGGATTGCGTC | 284434 |
rs536879123 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748994 | CATGTGGGTCTTTTC[A/G]AGACCCCCAGGTCAG | 284434 |
rs536891048 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16747589 | TTTTGCACAGGCTGG[G/T]CTCGAACTCCTGAGC | 284434 |
rs536896122 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16795047 | TTAGCCTCCCAAAGT[G/T]CTGGGATTACACAGG | 284434 |
rs536921441 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16731464 | GGCGTGCGCCACCAC[A/G]CCCAGCTAATTTTTG | 284434 |
rs536940618 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16754668 | ATTCTTCCTTGCATC[C/G]ATCATCTCTATCTTC | 284434 |
rs536943094 | snp | C/T | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749102 | CTGCTGACCCAATAA[C/T]GACCACACTTCCTTC | 284434 |
rs536958836 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16800587 | GCATAAGCAAGAAAC[A/G]TTATTCCTCAACATT | 284434 |
rs537029871 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16733588 | AAAAAGATGCATGAT[C/T]GTTATGGTTTGTATA | 284434 |
rs537039936 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16790999 | CACTTTGAGAGGCTG[A/G]GCAGGGAGGATAGTT | 284434 |
rs537086686 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16809270 | TGTGTTTTTAGTAGA[A/G]AAGGGGTTTTGCCAT | 284434 |
rs537185499 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16771618 | CTTCCCATTTTAAGG[A/G]AGATTTAAAAGCCCA | 284434 |
rs537186056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16796321 | ACAAAAATTAACTGG[A/G]CATGGTGGCAGGCGC | 284434 |
rs537191403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16764760 | GAAGAGATTCTGCCC[C/T]CCCAGGGGACACTTG | 284434 |
rs537212136 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16745524 | ACTTGAGTTCAGGAG[A/T]TCGAGACCAGCCTGG | 284434 |
rs537228987 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16740925 | GCACTTTGAGAGGCC[A/G]AGGCAGGCGGATCAC | 284434 |
rs537234781 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16730298 | CTGCACTCCAGCCTG[A/G]TGACAGAGTAAGACT | 284434 |
rs537236503 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816620 | GTGGATCTTTCTTCT[C/T]TGCCCACAGCCTTCT | 284434 |
rs537292410 | in-del | -/ATTTT | 0.0150606 | 0.0854603 | intron-variant | NWD1 | GRCh38.p7 | 19:16760570 | TGGCCAATTCACCAC[-/ATTTT]ATTTTATTTATTTAA | 284434 |
rs537295908 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16735767 | CCCATTAGGCAAAAT[G/T]TACAATGAGCCAAGA | 284434 |
rs537326682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16785238 | TGTGATAGGCCAGGC[A/G]CGGTGGCTCACGCAT | 284434 |
rs537329853 | in-del | -/A | 0.286042 | 0.247388 | intron-variant | NWD1 | GRCh38.p7 | 19:16729578 | ATCTTTACAAAAAGT[-/A]AAAAAAAAAAAAAAA | 284434 |
rs537354520 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16735114 | AGGCTTACAGGAAAC[A/G]CATGGACAGTACGGA | 284434 |
rs537371993 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16784486 | TGGATTTTGGTATCC[A/G]CAGGGGTGAAGGAAG | 284434 |
rs537377366 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16791872 | GGCAAGTGCCACCAC[A/G]CCTGGCTAATTTTGT | 284434 |
rs537379439 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16798126 | CTCAAACCTTGGGGG[A/C]AGATTTGTGCCTTCA | 284434 |
rs537389860 | snp | C/T | | | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718575 | GCTGGAGTGCAGTGG[C/T]GCAATCTCGGCTCAC | 284434 |
rs537421900 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16742623 | AAGGACCAGAACTAG[A/C]ATGGAGAACCACCAC | 284434 |
rs537455144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16780471 | AAAGGCAGGGTTTCA[A/G]GAAAACAAGTAGGCA | 284434 |
rs537460392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16787955 | CATCATAGGCCAGGC[A/G]CGGCGGCTCATGCCT | 284434 |
rs537463696 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16783943 | GTGGCCGGGCACAGT[A/G]GATCACGTCTGTAAT | 284434 |
rs537511795 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16806364 | GGGGATGTGGCCACC[A/G]CCCCTGAAATGGCCC | 284434 |
rs537518255 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16787214 | TCACTCCAGCCTCAA[A/C]CTCCTGCGCTCAAAT | 284434 |
rs537645590 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16771146 | CTCTGTAAAAAAAAA[A/T]TAATTAGTTAAAAAT | 284434 |
rs537705408 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16778045 | AGGGAGGGAAGGGGA[G/T]GAGAAGAAAGGAAAA | 284434 |
rs537771096 | in-del | -/AAAAG/AAAAGAAAAG/AAAAGAAAAGAAAAG | 0.0443703 | 0.143259 | intron-variant | NWD1 | GRCh38.p7 | 19:16808554 | GTTTAAAAAAAAAAG[lengthTooLong]AAAAGAAAAGAAAAG | 284434 |
rs537806590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16766785 | GAGACGGGATTTTGC[C/T]ATGTTTCACAGGCAG | 284434 |
rs537809758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16745810 | TAGCCCCAGCTACTC[A/G]GGAGGCTGAGATGAG | 284434 |
rs537870741 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16766080 | AACTATTTCGAGAAA[A/C]CTCGAGGAAATTATG | 284434 |
rs537886565 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16745721 | CTCCAGCCGGGGTTA[C/G]AGAGAGAGACCTGTC | 284434 |
rs537890096 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16769479 | AAAAAAAAGAGCCCA[A/T]ATCTCACTAAGTATC | 284434 |
rs537932089 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16772704 | GCTGAGTGTGGTGGC[A/G]CATGCCTGTAGTCCC | 284434 |
rs537998047 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16768960 | CTGTCTCTCCTCCAG[A/C]CAGCATCCTCGGAGG | 284434 |
rs538045595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16793223 | TTCTTTTTCTCAAGC[C/T]TCTTTGCAGATATTT | 284434 |
rs538046972 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16724765 | ATGGCGCCATCTTGG[C/T]TCATGCAACCTCTGC | 284434 |
rs538057508 | snp | A/C | 0.0894459 | 0.191631 | intron-variant | NWD1 | GRCh38.p7 | 19:16768314 | AATTTCCTTCCTTTT[A/C]AAGGCTAAGAATTTC | 284434 |
rs538089706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16733186 | TGATGGAGCCACTGC[A/G]CTCTAGCCTGGGTGC | 284434 |
rs538109389 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16798940 | TAGAATAAAATAATT[A/T]AAAAAAAAAAAACAT | 284434 |
rs538117272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16721058 | TTTCGCCATGTTGGC[C/T]AGGCTGGTCTCGAAC | 284434 |
rs538151037 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16740036 | CCACCTTGGATCACA[C/G/T]TTGTAATCCCAGCGC | 284434 |
rs538151876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16761403 | TTTTTTCTTTTTGGA[A/G]TCTCTCTCTGTTGCC | 284434 |
rs538161397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16805467 | CCAAAGTGCTGGGAT[C/T]AGAGGCGCACACCAC | 284434 |
rs538187221 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16774072 | TCTATCCATCCATCC[A/G]TCCACCGTCCTCCCA | 284434 |
rs538204210 | snp | A/T | 1.67323e-05 | 0.00289239 | intron-variant | NWD1 | GRCh38.p7 | 19:16763967 | GCTGCCCCCCATCTC[A/T]GAGGACCGAGCCTGG | 284434 |
rs538224210 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16731782 | TCTATCCATACTCTT[C/T]TAATGCTTTACTGTT | 284434 |
rs538229928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16726264 | ACAGCTCCTGGCCCA[C/T]GGCTCTATTTTTAAA | 284434 |
rs538241268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16729643 | GGTACTTTAGGGGGC[C/T]GAGGCACCTGAGGTG | 284434 |
rs538265620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16770393 | TGCTTCCCCTTCCAC[C/T]GTGATTGTAAGTTTC | 284434 |
rs538282816 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16738061 | AAAGGCAAGTGTGGC[C/T]TGCTGCCTGTCTTTG | 284434 |
rs538332941 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16769818 | CACTGCACCCTGTTT[G/T]CCATCTGTCTTGGCT | 284434 |
rs538335822 | snp | A/G | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817225 | GAATCACTTGAACCC[A/G]GGAGGCGGAGGTTGC | 284434 |
rs538343327 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16776529 | GCGGAGATCGTTCCA[C/G]TGCACTCCAGCCTGG | 284434 |
rs538360951 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817533 | CTTGAACCCGGGAGG[C/T]GGAGGTTGCAGTGAG | 284434 |
rs538425945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16752928 | TTGTTGAGCCAGGAG[A/G]TCATGGCTGCAGTGA | 284434 |
rs538429345 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16721505 | TGTGGTGGAGGCAAA[C/T]TCAAGATCAGAAGAT | 284434 |
rs538441228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16790471 | GAAATTCGGGGGGTA[A/G]GGGGTAAGGGGAGGG | 284434 |
rs538450036 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16761890 | TTTAGGATGGCTTGG[A/G]ATTTGGGAACTGCCT | 284434 |
rs538450354 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NWD1 | GRCh38.p7 | 19:16797125 | GCAGAGGTTGCAGTG[A/G]GCCAAGATCATGCCA | 284434 |
rs538477005 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16789420 | CCTTTCATCTTTTTT[A/G]AATATCAGCATTTTA | 284434 |
rs538490809 | snp | A/C | 8.25389e-05 | 0.0064236 | intron-variant | NWD1 | GRCh38.p7 | 19:16759199 | ACATGAGATGTGCCT[A/C]AAAGCCCCACTGGTC | 284434 |
rs538501619 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16767674 | ATGAGAACAGCATGG[A/G]GGAACCACCCCCATG | 284434 |
rs538524185 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16803038 | CACATGGCTGGGAAG[G/T]CCTCACAATCATGGC | 284434 |
rs538563409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16726711 | CCCAAAGTGCTGGGA[C/T]TATAGGTGTGAGCCA | 284434 |
rs538628554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16723567 | AATCCCCACCTCAGC[C/T]TCTCAAAGTGCCGAG | 284434 |
rs538653474 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16740996 | AAACCCTGTCTCTAC[C/T]AAAAATACAAAAAAT | 284434 |
rs538667480 | snp | C/T | 1.64735e-05 | 0.00286993 | utr-variant-3-prime, missense | NWD1 | GRCh38.p7 | 19:16815144 | GAGAATTTCCAGTGC[C/T]TTTCAGCAAAAGCCT | 284434 |
rs538708983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16722811 | TGGTTGACCTCTGGA[A/G]GGGCTGGGGATTAAG | 284434 |
rs538760594 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16772991 | GAAGGAGACAGGAGC[A/G]GACAGCAGAGGCCAG | 284434 |
rs538776602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800240 | AGGCTACTGTAACAA[A/G]TCATCCCCACAGGCT | 284434 |
rs538804753 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16747403 | TTTTTTTGAGACAAG[A/G]TCTTACTCTGTTGCC | 284434 |
rs538834437 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16731945 | GGTGGGACTGGGCGC[A/G]GTGGCTGACACCTGT | 284434 |
rs538835794 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16719134 | GTGAGCCACCATGCC[C/T]GGGTGATTTGTGAGT | 284434 |
rs538882587 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16796464 | AATCAATCAGGAAAG[C/G]GTGGGCAAACAGGAA | 284434 |
rs538884184 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751854 | AAGATAGTAAGAAAG[-/A]AAAAAAAAGAAGGAA | 284434 |
rs538897360 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718648 | GCTTCCTGAGTAGCT[A/G]GGACTACAGGTGCAA | 284434 |
rs538903215 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16741230 | TGCCAGTGCCTTAGT[A/C]GCTGTGCCCTTCCTA | 284434 |
rs538918909 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787400 | ACTCTTAGATGCTGA[A/T]TCTTTATAAAACTCA | 284434 |
rs538930175 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16802252 | CACTCCAGCCTGGGT[G/T]ACAGAGCAAGACTCT | 284434 |
rs538934574 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16782409 | AGTTGGAGGCTGCAG[A/T]GAGCCATGTTTGCAC | 284434 |
rs538957778 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16724090 | GAGTCTGTCCTGGGT[C/G]GACAAGGCAGGGAAG | 284434 |
rs538969528 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | NWD1 | GRCh38.p7 | 19:16751408 | ACAGGAAGGAAGGAG[A/T]CAGAAAGGAAGAGTG | 284434 |
rs538980975 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16764761 | AAGAGATTCTGCCCC[C/G]CCAGGGGACACTTGA | 284434 |
rs539016243 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16779858 | CCAGGCTGGTCTGAA[A/C]CTCTTGGGCTCAAGT | 284434 |
rs539056686 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16757178 | ACCCTGGTCCGCGGG[A/G]AAAAAATTGTCTTCC | 284434 |
rs539081413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16800800 | ACTTCCCTGTCACTC[C/T]GCTACAGTTCGGAGG | 284434 |
rs539096337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16754812 | TCCATCCATCCATCC[A/G]TCCATCCACACATCA | 284434 |
rs539098776 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16765971 | ACAGTGAGCCGAGAT[C/T]GCACCACTGCACTCC | 284434 |
rs539129356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16762969 | TTGTATTTTTAGTAG[A/G]GACGGGGTTTTGCCA | 284434 |
rs539137125 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16801681 | AGATTGTGCCACTGC[A/C]CTCCAGCCTGGACGA | 284434 |
rs539165411 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NWD1 | GRCh38.p7 | 19:16804575 | ACTCCAGCCTGGGCA[A/G]CAGAGACCCTGTCTC | 284434 |
rs539168861 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16763403 | CAAGCTCCCTACTCT[C/T]ATTTCCCACCCGCAT | 284434 |
rs539174819 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16719998 | CTAAATTGGTCGTTC[A/G]ACTACCAGCAAAGGC | 284434 |
rs539175371 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16788533 | AAGATTGAGCCACTG[C/G]ATTCCAGCCTGGGTG | 284434 |
rs539265957 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16780099 | CTCAACTTTGCTCCA[C/T]GTGGTCTGTCATCAT | 284434 |
rs539289114 | snp | C/T | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744638 | AGGCCACCTTAACTT[C/T]TGTCCTACGCTCTGG | 284434 |
rs539297320 | in-del | -/AATA | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16783656 | TAAAAATAATAAAAT[-/AATA]AATAAATAAAATAAA | 284434 |
rs539308893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16789616 | ATTTCTGGATAGGGT[C/T]CTGTTCTGTATTTTT | 284434 |
rs539333187 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16743893 | TCACTATGTTGGCCA[-/G]GCCAGTCTTGAACTC | 284434 |
rs539375210 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16795493 | ATGATCTCAGCTCAC[G/T]GCAACCTCCACCTCC | 284434 |
rs539405730 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815980 | TTCAGGTCACAAGTC[C/T]AAGGTGCAAGAGCTC | 284434 |
rs539454461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16784977 | AACAGCAGTCACCAG[A/G]GGCCACATGGTGTGC | 284434 |
rs539498805 | snp | A/G | 0.00439646 | 0.0466787 | intron-variant | NWD1 | GRCh38.p7 | 19:16735520 | CCCTGACCAAAAAAA[A/G]AAAGAAAGAAAGAAA | 284434 |
rs539518033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16784547 | CAGGGAGCAGCAAGT[A/G]CAAAGGCCCTGAGAG | 284434 |
rs539518238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16754151 | TTCATCCATCCGTCC[A/G]TCATCTCTATCTTCC | 284434 |
rs539537559 | snp | A/G | 3.29533e-05 | 0.00405901 | missense, synonymous-codon | NWD1 | GRCh38.p7 | 19:16797788 | GGCTTTCGCCGATTC[A/G]TGGCCATGGATCTGG | 284434 |
rs539604773 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16722311 | TTTTTTTTTTTTTGA[A/G]ACGGTCTTGCTCTGT | 284434 |
rs539731280 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16771859 | TTTTTTGAGAAGGAG[A/C]CTCGCTCTGTCACCC | 284434 |
rs539776506 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16792984 | TAGGAGGTGGAGGCT[A/G]CAGTGAGCCAAGATT | 284434 |
rs539790005 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16778788 | TTTGGCCTCCCAAAG[A/T]ATTGGCCTCCCACAG | 284434 |
rs539803033 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16806499 | CAAAGGTGGGAGGAT[C/T]GTTTGAGCCCTGGAG | 284434 |
rs539824255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16743737 | GCCCAGGCTGGACTG[C/T]GGTGGCACCATGTCG | 284434 |
rs539840352 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | NWD1 | GRCh38.p7 | 19:16808614 | GTTTTTTTTGTTTTC[A/T]TTTTTTTTTTAAAGA | 284434 |
rs539888379 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16812366 | GTGTCTTTCAGTTTG[G/T]AATCAAGATCATATT | 284434 |
rs539890708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16727037 | TGGGGTGGGACTTTC[A/G]TCAAGCGGTTGTCTT | 284434 |
rs539891262 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16760742 | TTTACAAGCATGAGC[C/T]ACCACACCCAGCTAA | 284434 |
rs539911912 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16767319 | GGAGCAACTGCCTTA[C/T]AAAACCATCGGACGG | 284434 |
rs539928453 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16811571 | CCAGGGCAACAAGAG[C/T]GAGACTCTGTCTCAG | 284434 |
rs539953777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16732330 | GCTTTTGAACACAGA[C/T]TCATCGCTGTGTCCC | 284434 |
rs539997897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16759958 | AAGATCGCACCACTG[C/T]ACTCCAGCCTGGCAA | 284434 |
rs539999809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16765965 | GAGGTTACAGTGAGC[C/T]GAGATCGCACCACTG | 284434 |
rs540019398 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16803785 | AAAAAATTATCTGGG[C/T]GTGGTGGTGTGTGCC | 284434 |
rs540063086 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16765305 | CTCATACCTTTCCTG[C/T]CTAAACATGTGAATT | 284434 |
rs540085810 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16796745 | CTCCTTCCTCCCTTC[C/T]TTCCATCATAGTTAT | 284434 |
rs540095557 | snp | C/G | 0.00358031 | 0.0421585 | intron-variant | NWD1 | GRCh38.p7 | 19:16794442 | TGGAAGTGCCTGACA[C/G]GCATCCCTGGTTCTG | 284434 |
rs540156756 | in-del | -/A | 0.339429 | 0.233457 | intron-variant | NWD1 | GRCh38.p7 | 19:16798939 | TAGAATAAAATAATT[-/A]AAAAAAAAAAAAACA | 284434 |
rs540175748 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16771391 | GGAGGCAGATGTTGC[A/G]GTGAGCCGAGATCAC | 284434 |
rs540192365 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16758836 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 284434 |
rs540198771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16768406 | TCATCTGTCTGTGGA[C/T]ATTTGTGTGTTTCTA | 284434 |
rs540200234 | snp | C/T | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817341 | CTCGGTGGCTCACGC[C/T]TGTAATCCCAGCACT | 284434 |
rs540205310 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16727562 | TGGGCGGCAATGAGC[A/G]TGGGCCCTCTCAGCC | 284434 |
rs540226493 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16767816 | CTCCCTTCACCCCAG[A/T]CCCTGGCAACCACCA | 284434 |
rs540279699 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16806812 | TTGAGGTCAGGAGTT[A/C]AAGACCAGCCTGGCC | 284434 |
rs540287452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16774184 | CTTCCCACTCTCCCA[C/T]CCATCTATCCTCCCA | 284434 |
rs540292757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16755031 | CATCTGTCTATACCT[A/G]TCTAACTCTATATCT | 284434 |
rs540316438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16760926 | GAGTGGTATTTTAGT[A/G]CACTCATAATGTTGC | 284434 |
rs540385375 | snp | C/T | 8.51057e-05 | 0.0065227 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750316 | CCCGCTGGCCACCAC[C/T]GCAGAGGAAGCCACG | 284434 |
rs540435819 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16808615 | TTTTTTTTGTTTTCA[-/T]TTTTTTTTTAAAGAG | 284434 |
rs540461169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800273 | GCCCCATGGCTCACG[C/T]CTGTAATCCCAGGAC | 284434 |
rs540509330 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16762516 | TGGCCATACTGGTCT[C/T]GAACTCCTGCCTGGG | 284434 |
rs540542329 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16786128 | CCTTGGCCTTCCAAA[C/G]TGTTGGGTTTACAGG | 284434 |
rs540588366 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787272 | GCTAGGACCACAGGT[A/G]CATGCCACCCCACCT | 284434 |
rs540601086 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16799102 | CCTGAGTAAGTTAAA[C/G]GAATGGGAAGATGTG | 284434 |
rs540620772 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16752674 | CAGGGGACATATCCC[A/T]GATTTCCCGACTGGC | 284434 |
rs540681981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16720715 | GTCCGCCACATGCCC[A/G]GCTAATTTTTTGTAT | 284434 |
rs540702025 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16775799 | CAGCCTCCCAAGTAG[C/T]TGGGATTACAGGCAC | 284434 |
rs540734863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16726352 | CTGGCTCAAGAGATC[C/T]TCCTGCCCTGGCCTC | 284434 |
rs540736483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16764841 | TGGTATCTGGTGGGT[A/G]GAGGCCAGGGTTGCT | 284434 |
rs540755272 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16769907 | CAATGGCATGATCAT[A/G]GCGCACAGCACCTTC | 284434 |
rs540795667 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16745351 | AAGACACAGCCAAAC[C/G]ATATCAGGGGGAGCA | 284434 |
rs540795748 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16738726 | CAAAACATATATATA[A/T]AATCTATATATAATA | 284434 |
rs540861274 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16744050 | GAAATAAGGACCCAC[A/G]AAAGCAGCTAGAGTC | 284434 |
rs540862130 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16796167 | AGCATTATTCAGGCC[A/G]GGTGCAGTGGCTCAC | 284434 |
rs540881471 | in-del | -/AAA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16739330 | GACCCTATCTCTACC[-/AAA]AAAAAAAAAAAAAAA | 284434 |
rs540916512 | snp | C/T | 0.000140696 | 0.0083862 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744461 | CCTGTCTGATTCCCT[C/T]GCGGATCGATGAGAA | 284434 |
rs540939643 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16723457 | TGGGATTACAGGCGT[A/G]AGCCACCAAGTCTGG | 284434 |
rs540966708 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16747471 | GGCCTCCAGCTCCTG[C/G]GGTCAAGCAATCCTC | 284434 |
rs540982217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16747014 | TTCCACCTCTGTCTA[A/G]TTCCAAGATATTTTC | 284434 |
rs540982894 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16790491 | TAAGGGGAGGGAGAG[A/C]ATTAGGACAAATACC | 284434 |
rs541018631 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718743 | CCATGTTAGCCAGGA[A/T]GGTCTTGATCTCCTG | 284434 |
rs541043841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16751901 | AGAAAGAAAGAGAAA[A/G]AGAGAAAAAGGGAAA | 284434 |
rs541059145 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16728812 | AGCTAGGCGTGGTGG[C/T]GGGCGCCTGTAGCCC | 284434 |
rs541076561 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16756465 | CTCATGCAGTTCAAA[C/T]CTGTGTTCTTCAAGG | 284434 |
rs541083975 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718214 | TAGTGTGGCTCTGTC[G/T]TCCAGGCTGGAGTGC | 284434 |
rs541141566 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16778946 | ATGGGGTTGTCATGC[A/G]TTGCTGGGTGTTGAA | 284434 |
rs541147031 | in-del | -/T | 0.0228336 | 0.104381 | intron-variant | NWD1 | GRCh38.p7 | 19:16731316 | TCCATGCTTTTTTTA[-/T]TTTTTTTTGACACGT | 284434 |
rs541172574 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815495 | TTCCATTATTCTTTC[C/G]TCTTTTTCATTTTCA | 284434 |
rs541183191 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16795117 | CAGGATTTTTCTTGG[C/G]CTCTTTGCCAAGCTG | 284434 |
rs541194832 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16743355 | ACCTGAGACTACAGA[G/T]GCACACCCCCACACC | 284434 |
rs541195817 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16747069 | TGAGATGGAGTCTTG[C/T]TCTATTGTCCAGGCT | 284434 |
rs541200631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16735335 | ATAGCAAAACTTTAT[C/T]TCTAATAAAGATACA | 284434 |
rs541266294 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16769899 | CTGGAGTGCAATGGC[A/G]TGATCATAGCGCACA | 284434 |
rs541348164 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16813816 | CCACTTTGGAAACAC[C/T]GTGTCTCTTGGTCTG | 284434 |
rs541400152 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16737792 | GCCTGGGCAACATAG[C/T]GAAGTCCCATATCTA | 284434 |
rs541430447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16782469 | AGACCTTGTTTCCAA[A/G]AAACCAAACAAACAG | 284434 |
rs541459848 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16737246 | TTTGGCTATTAAAAT[G/T]GAATGATATTCCTGA | 284434 |
rs541467752 | in-del | -/TGT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16741366 | TTTGTTTTGTTTTTG[-/TGT]TGTTTTTTTTTTTTT | 284434 |
rs541482619 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16769622 | TCCTTACTGCCCCAG[A/G]CAGTGATGGAAACAT | 284434 |
rs541536282 | in-del | -/AAAC | 0.0019992 | 0.0315532 | intron-variant | NWD1 | GRCh38.p7 | 19:16812672 | GAAACTCCATCTCAA[-/AAAC]AAACAAACAAACAAA | 284434 |
rs541551263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16788363 | CGCTTGAGGCCAGGA[A/G]TTCAAGGCCAGCCTC | 284434 |
rs541558726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16743972 | ACAGGTGTGAGCCAC[C/T]GCGCCTGGCCGATAT | 284434 |
rs541564928 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16792308 | ACTTTGGGAGGCTGA[-/G]GGGGGGGTGGATCAT | 284434 |
rs541574593 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | NWD1 | GRCh38.p7 | 19:16752215 | TTCTCAGTTTTAGGG[-/T]TTGTTTTTTTTTTTT | 284434 |
rs541574924 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16785447 | ATCCTGGAGTGGGAG[G/T]TTGCAGTGAGCCGAG | 284434 |
rs541602040 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16801200 | AGAAGAATAGCTTGA[A/T]CCTGGGAGGCAGAGG | 284434 |
rs541640963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16720804 | ATGATCTGCCCTCCT[C/T]GGCTTCCCAAAGTGC | 284434 |
rs541652163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16728667 | AAGTAATTGCAGGCC[A/G]GGTGCAGTGGCTCAC | 284434 |
rs541694637 | snp | C/T | 0.000349049 | 0.0132062 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807734 | GATATGCATTCCCCC[C/T]CCCGAGGCCCGGAAA | 284434 |
rs541696315 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16813900 | CTCAAGCCTGCAATC[C/T]CAGCACTTTGGGAGG | 284434 |
rs541703406 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16726522 | TTAGTTCACTGCAAC[C/T]TCCACCTCCTGAGTT | 284434 |
rs541720124 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790468 | CTTGAAATTCGGGGG[A/G]TAGGGGGTAAGGGGA | 284434 |
rs541845272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16744306 | CACTTAAACCCAGGA[A/G]GTTGAGGCTGCAGTG | 284434 |
rs541906899 | snp | A/G | 9.09479e-05 | 0.00674283 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749098 | TCAGCTGCTGACCCA[A/G]TAATGACCACACTTC | 284434 |
rs541922888 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16792503 | CCAACATGAAGAAAC[C/T]TCATCTCTACTAAAA | 284434 |
rs541926436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16771306 | AATACAAAAATTAGC[C/T]GGGTGTGGTGGTGCA | 284434 |
rs541945236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16778134 | TTCTCAGAGCTTGAC[A/G]GGCTCTGATTCAGCA | 284434 |
rs541973218 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816056 | TTCAGTCTGCAGAGC[A/G]CAACCATCTCTTCCA | 284434 |
rs541990640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16726865 | ACGTGATGCCAGTAG[C/T]ATCCTCCAGTCGTGG | 284434 |
rs542071781 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16739855 | GGAACTGTTCCTATT[G/T]CCCTTGCTCTGATCC | 284434 |
rs542112341 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764045 | CAAACATGGAAATCC[A/T]TCGTTCCTCCTAAGG | 284434 |
rs542113502 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16773396 | GAAGGCCAGGTGTTT[C/G]AGGTTGTCCTCTGGG | 284434 |
rs542123183 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16818205 | GGGGCCAAGGTGGGA[A/G]GATCACTTGAGCCCA | 284434 |
rs542136926 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16719589 | GTGCAGAGTAGTGAA[C/G/T]CGTCACAGGCAAGGG | 284434 |
rs542142624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16804045 | TTTAATTCAGGTTAC[C/T]TAGAAGCTGAATCTG | 284434 |
rs542168450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16809862 | GTGCCTGGCTGCTCC[A/G]TGCTATTTCTTTATC | 284434 |
rs542174856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16773041 | TCTTTTGTTCTGGAG[C/T]CCCTGCAGGGAGCAG | 284434 |
rs542339161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16770703 | CTGGGAAGAGTACGC[A/G]CATCAGTTCACACAG | 284434 |
rs542350499 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16808230 | ACACCATGGGCCATC[A/G]ACCAGGATGGGACTG | 284434 |
rs542354281 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NWD1 | GRCh38.p7 | 19:16736011 | ACATGACTGTTAACC[C/T]CCTGACTTTATTCAA | 284434 |
rs542404756 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16767976 | GCATATGTCAGAATT[C/T]CCTTCCTTTTTTTTT | 284434 |
rs542456749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16754235 | CCATCTATCCATCCA[C/T]CCATCATCTCCATCT | 284434 |
rs542463713 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16720067 | GACACTGCAAAGGGC[C/T]TCTGTCCTTACTGGG | 284434 |
rs542519847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16753470 | TTACACATCAGATCC[A/G]TGTGGCAGGATGGTG | 284434 |
rs542536739 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16794827 | TGCTGTGTCACCCAG[A/G]CTGGAGTGGAGTGGC | 284434 |
rs542565606 | snp | C/T | | | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16719336 | AGATAGGGGTCTCAC[C/T]ATATTGGCCAGTCTG | 284434 |
rs542586046 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16759641 | CAGCACTTTGTGGGG[C/T]CAGGGCAGGAGGATT | 284434 |
rs542614199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16745011 | TTCTCATGCCACTAA[C/T]AAAGGCATACTTGAG | 284434 |
rs542627427 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16756217 | AGATCACGCCATTGC[A/T]CTTGAGCCTGGGTGA | 284434 |
rs542633232 | snp | A/G | 1.66349e-05 | 0.00288395 | synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749560 | CCTTTGGCAGAGCTC[A/G]GAGGTCATTCAGACC | 284434 |
rs542645682 | in-del | -/G | 0.00557542 | 0.0525036 | intron-variant | NWD1 | GRCh38.p7 | 19:16793111 | ATCCCAAATCCCAAA[-/G]CTCCACATTTCTGAA | 284434 |
rs542674697 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16768453 | AAAAGGAATCACTAG[A/C]TCACATGGAAATTTT | 284434 |
rs542689903 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16727837 | AGGCTGAGGCGGGTG[A/G]ATCACTTGAGGTCAA | 284434 |
rs542690847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16755544 | CAGGCGTGCACCACC[A/G]TGCCTGGCTAATTTT | 284434 |
rs542709854 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16746109 | CCTGTAATCCCAGCA[A/C]TTTGGGAGTCTGAGG | 284434 |
rs542716813 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817694 | TTTTCATTTAACTGA[C/T]TTAACTGAAGAGCCC | 284434 |
rs542718094 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16793467 | CTGGTTTCAAACTTA[C/T]GGGCTCATTCAGCCT | 284434 |
rs542721784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16813039 | CATGCTCTGGAGTTC[A/G]AGAACTCCCTCCCTT | 284434 |
rs542741345 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16799727 | TGGTCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 284434 |
rs542743147 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16771913 | CGATTCTCCTGTCTC[A/G]GCCTCCCGAGTAGCT | 284434 |
rs542757359 | snp | A/C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16796953 | GAAGTCCGAGGTGGG[A/C/T]GGATCACTTGAGATC | 284434 |
rs542757384 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16733326 | AGGAGTTCGAGACCA[C/G]CCTGGCCAACATGGT | 284434 |
rs542764637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16746402 | ACAGTTGGCCGGGTG[C/T]GGTGGCTCATGCCTG | 284434 |
rs542775710 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16768292 | TGAGCTACCATGCCT[A/G]GCTAAGAATTTCCTT | 284434 |
rs542803146 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16781442 | GCAACATGGTGAACC[C/T]ACATCTCTACAAAAA | 284434 |
rs542807546 | snp | A/G | 1.64732e-05 | 0.0028699 | missense | NWD1 | GRCh38.p7 | 19:16789038 | GCCAACTCTGCTTCA[A/G]AGGATTACACGCTGC | 284434 |
rs542808304 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16812496 | CAACATGGTGAAACC[C/G]CATTTCTACTCAAAA | 284434 |
rs542821529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16774246 | ATCCACCCACCCATT[C/T]ATACATCAGTTGTCC | 284434 |
rs542828388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16740221 | GGAAAATCCCTTGAG[C/T]CCAGAAGTCTGAGGT | 284434 |
rs542879983 | in-del | -/TC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16773855 | CCATCCATTCATTCA[-/TC]TCTCTATCTACCTCC | 284434 |
rs542886691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16780699 | GTGTTGCTCTGTTGC[C/T]CAAGCTGGAGTGCAG | 284434 |
rs543007759 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16794257 | TGTAATCCCAGCTAC[G/T]TGGGAGGCTGAGGCA | 284434 |
rs543032150 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16753140 | TCTCCTTCCTTCTCC[A/C]TCTGGGGTCCTCTCT | 284434 |
rs543042799 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16766844 | TCCTGCCTCAGACTC[C/T]CAAAGTGCTGGGATG | 284434 |
rs543050344 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16781263 | GGAGAGATGATTCCC[A/G]CAGTAGAGTTCATAA | 284434 |
rs543074782 | snp | C/T | 0.000846396 | 0.0205544 | utr-variant-3-prime, synonymous-codon | NWD1 | GRCh38.p7 | 19:16815258 | GGAGCTCCCCAGGAC[C/T]TGGAGTCAGAAAGTG | 284434 |
rs543105295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16799714 | GGTTTCTCCATGTTG[A/G]TCAGGCTGGTCTCGA | 284434 |
rs543107654 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16752714 | ATAAGAGTACAAATA[A/C]GGCGTGGTGTGGTGG | 284434 |
rs543128593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16721104 | ATCTGCCTGTTTTGG[C/T]CTCTCAAAGTGCTGG | 284434 |
rs543148811 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16761544 | GTATTCTTTTTTTTA[A/G]TACAGACAGGGTTTC | 284434 |
rs543167669 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16733994 | GGGAGGCAGGGACTG[C/T]TCCGAGTTGTCTTTG | 284434 |
rs543220278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16771379 | TGCTTGAACCCGGGA[A/G]GCAGATGTTGCGGTG | 284434 |
rs543222540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16727612 | TCTGCGGGGTGAAGC[C/T]GGCCCCCTCCCAGCA | 284434 |
rs543238022 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16739670 | GCGCCTTCCACAAAA[A/G]TCAGAGATGTGCTGG | 284434 |
rs543284665 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16736267 | CAGAGCCTGGCTCTG[C/G]TGTCCAGGCTGGCAT | 284434 |
rs543285885 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16725485 | TCTGTATCACCTAAC[A/C]ACAAACCTCCTGCAG | 284434 |
rs543287120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16778252 | TAGTGTCTAGGCCCA[C/T]GTTTTCTCCAATATA | 284434 |
rs543342424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16787501 | GCTTTGCCACATTTC[A/G]TTATTTTCCATTTGG | 284434 |
rs543382853 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16734549 | CAAAAAAAAAAAAAA[G/T]ATTTTCTTTCTTTTT | 284434 |
rs543404629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16784279 | GCTGAGGCAGAAGGA[C/T]CGCTTGAGCCTGGGA | 284434 |
rs543444237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16734123 | CAAGCGTGCGGTTGC[C/T]AAGGAGACCTTGGTA | 284434 |
rs543449765 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16771690 | CCTGTGGCTCCCCCA[G/T]CACAAGGAGGAGGTG | 284434 |
rs543484133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16742129 | CCTGTAATCCCAACA[C/T]TTTGGGAGGCTGAAG | 284434 |
rs543549481 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16746682 | GTCTAAAAACAAAAA[A/C]CAAAAAACAACAAAA | 284434 |
rs543590393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16789851 | GGCTCCTGAATAGCT[A/G]GGACTACAGGCGCAC | 284434 |
rs543595337 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817011 | TATTAAAAATAATGG[C/T]AAAAACTGGCTGGGC | 284434 |
rs543609102 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16758961 | GTGAGCCGAGATTGC[A/C]CCACTGCACTCCAAC | 284434 |
rs543658502 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16729792 | GAGAATCCCTTGAAT[C/G]TGGTAGGCGGAGGTT | 284434 |
rs543682662 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816186 | AAGGCAGAGATTGTG[C/T]CTAGGGTGGGTATGA | 284434 |
rs543716968 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16805724 | TGCTCCCTGCCAACC[C/G]CCAGAGCTTTGCCTA | 284434 |
rs543718627 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16729175 | GTGAGTGGCATACGA[G/T]GTTACAACTAATATT | 284434 |
rs543755904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16814831 | ATCTTAAAAATCGCC[C/T]TGAGCAGGTGTAGGT | 284434 |
rs543761008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16811498 | TTGAGGCAAGAGAAT[C/T]GCTTGAACCCAGGAG | 284434 |
rs543850126 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16818252 | GTTAGCTATGATCGC[A/G]CCACTGCACTCTAGC | 284434 |
rs543886558 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817711 | TAACTGAAGAGCCCA[A/C]TTAAATTGTGAAGGG | 284434 |
rs543894616 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16741439 | GGCACCATGTCGGTT[C/T]ACTGAAACCTCCCTC | 284434 |
rs543909434 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16723047 | TTGGATGCCTCTTCC[A/T]GTGCCTGATCTTATT | 284434 |
rs543966797 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16791190 | AGTGAGCCATGATTG[C/T]ACCACTGCACTCCAG | 284434 |
rs543967317 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16792078 | GAAACATCTGTTGGC[A/G]TCTCTTGGGGACTGA | 284434 |
rs543976350 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16737914 | AGGTTGCAGTGAGCC[A/G]AGATCATGCCACTGT | 284434 |
rs543981823 | snp | A/C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718425 | TGATTTGCCCACCTC[A/C/G]GCCTCCCAAAGTGCT | 284434 |
rs543989009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16721892 | GAGGCAGGAGGATGG[C/T]TTGAGGCCAAGAGTT | 284434 |
rs544006187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16779779 | GTAGCTGGGACTACA[A/G]GCACATACCACTATA | 284434 |
rs544013603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16758215 | ATGCAACCAAGAAAC[C/T]GCATTTTGAATTTTA | 284434 |
rs544049506 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16721357 | AGCCTAGAGGTGAAA[G/T]GCAAGGTCAAAGACT | 284434 |
rs544074252 | snp | C/T | | | synonymous-codon | NWD1 | GRCh38.p7 | 19:16762021 | CTACCTGTCAGGATC[C/T]GAGAGAGCCAAGAGG | 284434 |
rs544076417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16763730 | GCATTCTCGTCCACT[C/T]CAGCACTGTCTGGAG | 284434 |
rs544089935 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16768633 | AGAAAGGGCTCACAC[A/G]TTTTAATTTTACATG | 284434 |
rs544109908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16727005 | TTGCCTCGTGGGAGG[A/G]GGTGGGAAGGGCAGA | 284434 |
rs544117478 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16812338 | GCCTGGTTCCTTGGG[C/G]CTGGTTTCCTGGGTG | 284434 |
rs544173239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16732284 | CTTGGTTAGCATGGC[A/G]GGTGGTGTAGAAAAG | 284434 |
rs544174186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16769971 | GCCTCCCAAGTAGCT[A/G]GGACCACAGGTGCAC | 284434 |
rs544183011 | snp | C/T | 8.27465e-05 | 0.00643167 | missense, utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16797876 | CGGGGTCCCTTGATG[C/T]GCTCATTCAGGTGAG | 284434 |
rs544188833 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16772703 | AGCTGAGTGTGGTGG[C/T]GCATGCCTGTAGTCC | 284434 |
rs544197959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16805847 | CATCATTAACAAGGA[A/G]TTTCTTTTTTCTTTT | 284434 |
rs544237003 | snp | G/T | 0.125528 | 0.21681 | intron-variant | NWD1 | GRCh38.p7 | 19:16738629 | ATTTTCTGAGATCTA[G/T]TTTCTGAGACCTAAA | 284434 |
rs544238521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16773455 | AGCTTGCCATCAGAG[C/T]CTGCCCCTGCTGTCT | 284434 |
rs544281046 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16765533 | GAGACAGGGTCTCAC[G/T]GTGTTGCCCAGGCTA | 284434 |
rs544298936 | snp | G/T | 5.01702e-05 | 0.00500825 | intron-variant | NWD1 | GRCh38.p7 | 19:16773078 | AATTGGCAGGGAGGG[G/T]AGAGGGGGCTCAATC | 284434 |
rs544301733 | snp | A/G | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16760081 | GATCACTTGAGCCCA[A/G]GAGTTTGAGGCCACA | 284434 |
rs544326518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16786509 | CTCCTTCCCCATTCC[A/G]GTAGTCCCCAGTATC | 284434 |
rs544329395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744780 | ACGTGTTCAGAATAT[C/T]CATCCCCTGTTGGCA | 284434 |
rs544378282 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16799764 | CCACCTGCCTCAGCC[A/T]CCCAAAGTGTTGGGA | 284434 |
rs544415980 | snp | C/T | 0.000313503 | 0.0125161 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16762051 | GCATGGCGTCCTGGC[C/T]GACTTCTTCTCAGGG | 284434 |
rs544425710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16806432 | GGCCCCCTTGCTTCA[A/G]GATGGGACAATTCAT | 284434 |
rs544463100 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16792573 | TGTAATCCCAACTAC[C/T]TGGGAGGCTGAGGCA | 284434 |
rs544474081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16786087 | CCAGGCTAGTCTCGA[A/G]CCCCTGACCTCAACT | 284434 |
rs544501430 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16767704 | GATCCAATCACCTCC[C/G]ACCTGGTCCCTCCCT | 284434 |
rs544529334 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16743930 | TCAGGTAATCCACCC[A/G]CCTTGGCCTCCCAAA | 284434 |
rs544562862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16767265 | GCTCACTGCAAGCTC[C/T]GCCTCCTGGGTTCAT | 284434 |
rs544665191 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16725651 | TCCGCCTCCCAGGTT[C/G]AAGCGATGCTTCCGC | 284434 |
rs544672316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16801807 | AAGGACACATCCCTC[A/G]TGGATAGATTAATGC | 284434 |
rs544689988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16763268 | CAAGGATGCTTCTGA[C/T]CATCCAATCTGATTA | 284434 |
rs544720106 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16784908 | CACTCCAGCCTGGGC[A/G]ATGACAGAGTGAGAC | 284434 |
rs544728680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16725114 | TGCCTCCCAGGTTCA[C/T]GCAATTCCCATGCCT | 284434 |
rs544736210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16764894 | GTTCAGCCCCTTACC[A/G]CAGAGAATGATCCTG | 284434 |
rs544856503 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16803360 | CCAGCTCCTAATACC[-/A]TCCTATGGGGAGTGA | 284434 |
rs544856799 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764445 | TCTATGATCTCCTTA[C/T]TGAGCCATGAGCTGG | 284434 |
rs544884708 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16754921 | TCTATGTCTATCTCT[A/G]TATATCTATATATTT | 284434 |
rs544913851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16742132 | GTAATCCCAACACTT[C/T]GGGAGGCTGAAGCAG | 284434 |
rs544913966 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16720581 | TTTTTTTTTGAGACG[C/G]AGTCTCGCTCTGTCA | 284434 |
rs544942490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16751085 | AAAAATTAGCCAGGC[A/G]TGGTGGTGCATGCCT | 284434 |
rs544966413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16751828 | AAAGAGAAGGAAGGA[A/G]GGAAGGAAGGAAGAT | 284434 |
rs544998233 | in-del | -/CC | 0.000474634 | 0.0153978 | intron-variant | NWD1 | GRCh38.p7 | 19:16762161 | CCTGGGACCCCCATT[-/CC]CCCCACCTGCAACCT | 284434 |
rs544998324 | in-del | -/C | 0.00517822 | 0.0506191 | intron-variant | NWD1 | GRCh38.p7 | 19:16801864 | GTGAGTAAGTTCTAA[-/C]TCTGTTAGTTCTCGC | 284434 |
rs545026558 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16770680 | AGTGACCATCCCACC[C/T]AGGGCTGCTGGGAAG | 284434 |
rs545031903 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16801141 | AAAATTAGCTGGGCG[C/T]GGTGGTGCATGCCTG | 284434 |
rs545069260 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16780978 | CTTCATTTTTTGATG[C/G]GAGGAGCTGCAAAGT | 284434 |
rs545091256 | snp | C/T | 0.000100546 | 0.00708964 | missense | NWD1 | GRCh38.p7 | 19:16750021 | CTCTCAACTGCCCCC[C/T]GAGGGTGCACCTCAT | 284434 |
rs545116159 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16775707 | GAGTTTTGTTCTTGT[C/T]GCCCAGGCTGGAGTG | 284434 |
rs545140714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16722446 | AGGCATGAACCATCA[C/T]GCCCAGCTAATTTTG | 284434 |
rs545184694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16783490 | AAATACAAAATTAGC[C/T]GGGCGTGGTGATATA | 284434 |
rs545191851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16742183 | AATTCGAGACCAGCC[C/T]GGCCAACATGGCGAA | 284434 |
rs545197405 | snp | A/C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16740259 | AACTATGATTGTACC[A/C/G]TGGCACTCTGGCCTG | 284434 |
rs545259205 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16753147 | CCTTCTCCCTCTGGG[G/T]TCCTCTCTGCACATC | 284434 |
rs545264819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16773403 | AGGTGTTTGAGGTTG[C/T]CCTCTGGGACTCCCC | 284434 |
rs545287877 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16793694 | CGATTCTCCTGCCTC[C/T]GCCTCCCCAGTAGCT | 284434 |
rs545312169 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16746464 | CGGATCACGAGGTCA[C/G]GAGTTCAAGACCAGC | 284434 |
rs545345606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16756310 | CATGAAGTGGAAGTG[A/G]ATATCACAAAGGTCT | 284434 |
rs545347859 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16779850 | TATGTTGCCCAGGCT[G/T]GTCTGAAACTCTTGG | 284434 |
rs545474819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16794667 | AGGTTAGCAACGTTT[C/T]CTGCCAAATGGCCTC | 284434 |
rs545476866 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16787598 | GGCACAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 284434 |
rs545537872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16794298 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC | 284434 |
rs545632505 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16731101 | AAGGGGAAAAAAGAC[-/A]AAAGTAAATCAATAA | 284434 |
rs545660707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16813128 | CTGGGCTCCTGGTGT[A/G]TGCACTTCTGGGCTC | 284434 |
rs545687553 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16740382 | ACTCTGTCACCCAGG[C/T]TGGGGTGCAGTGGGA | 284434 |
rs545716277 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16781547 | CTTGAGCTCAGGAGA[C/T]TGGGGCTACAGTGAG | 284434 |
rs545716947 | snp | G/T | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16731235 | GAGCACTGCCTACCC[G/T]GAAGTGCCAGACCTT | 284434 |
rs545728902 | snp | A/C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16720201 | ACTATGTGCCAGGCA[A/C/T]GCCAGCCTTACCAGA | 284434 |
rs545745353 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16772108 | CAGTGGCTCACGCCT[A/G]TAATTCCAGAGCTTT | 284434 |
rs545746866 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16736349 | ATCCTCCTACCTCAG[A/C]CTCCCGAGTAGCTGG | 284434 |
rs545751829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16808965 | TGATGTGCACCTGTG[A/G]TCCAGCTACTTGGAG | 284434 |
rs545765890 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817067 | GCTCTTTGGAAGGCC[A/G]AGGCAGGTGGATCAC | 284434 |
rs545812237 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748585 | TAATCCCAGCACTTT[G/T]GGAGGCCGAGGTTGA | 284434 |
rs545853781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16729959 | AAAGAAAGATTTGTC[C/T]CTGTTATTCTCTAGC | 284434 |
rs545868511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16784713 | AGGTGGGCAGATCAC[A/G]AGGTCAAGAGATCGA | 284434 |
rs545875237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16814874 | CCCATTGTGCAGATA[A/G]AGGAAGAGGGACTCT | 284434 |
rs545952529 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16776751 | CTGGGCAACATAAGG[A/T]GACCTTGCCTCTACA | 284434 |
rs545959166 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16731470 | CGCCACCACGCCCAG[A/C]TAATTTTTGTATTTT | 284434 |
rs545978903 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16810549 | GAGGCAGGGGGATTG[C/T]TTGAGCTCAGGATTT | 284434 |
rs545980796 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16804316 | CCAGGTGTGGTGGCT[C/T]ATGCCTGTAATCCCA | 284434 |
rs545989481 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16772936 | GACTGGAAACAGCTG[C/G]GTGCCTCTGAAGCAA | 284434 |
rs546041080 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16724880 | TGTATTTTTAGTAGA[G/T]ATGGGGTTTCACCAT | 284434 |
rs546041779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16753299 | TCCTAATTCCAAAGT[A/G]CAGGGAGACAGAAAT | 284434 |
rs546057276 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16814054 | TCCCAGCTACTCAGG[A/C]GGATAAAGTGATCAT | 284434 |
rs546068342 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16810024 | GAAGACACAGTGAGC[A/T]CTGTCTGGGCAAAAG | 284434 |
rs546084249 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16758871 | AAATTAGCCAGGCGT[G/T]GTGGCGCCTGTAGTC | 284434 |
rs546158991 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16747040 | TTTCTTTTTCTTTCT[-/T]TTTTTTTTTTTTTTG | 284434 |
rs546171059 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16784456 | ACTATTTCGTATAAG[A/G]CACTGGAGCATCTGT | 284434 |
rs546216084 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16729386 | CATATCAGGACTATC[A/T]CTCTCACGGTTCCCT | 284434 |
rs546229528 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16770654 | TTCCCATCTGCAGAA[C/T]AGGGATGCTGAGTGA | 284434 |
rs546280951 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16755261 | ACTCTCTTGACCCAG[A/C]CTGGAGTGCACTGAA | 284434 |
rs546305315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16798721 | AACCTCGACCTCCTG[A/G]GTTCAAGCAATTCTC | 284434 |
rs546372971 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16767416 | GGTCAGGAGTTTGAG[A/T]CCAGCCTGGCCAACA | 284434 |
rs546401905 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16752769 | TGGGAGGCCAAGGTG[A/C/G]GAGAATTACTTGAGC | 284434 |
rs546413357 | in-del | -/A | 0.00636936 | 0.0560724 | intron-variant | NWD1 | GRCh38.p7 | 19:16777862 | GAAAGGGAAGGGAAG[-/A]GGGGGGAAGGGGAGG | 284434 |
rs546441999 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16759496 | GAGGACTCACTGGCC[G/T]GGGGTCTTCTCAGTA | 284434 |
rs546481591 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16781433 | CCAGCTTGGGCAACA[G/T]GGTGAACCCACATCT | 284434 |
rs546507289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16764763 | GAGATTCTGCCCCCC[C/T]AGGGGACACTTGACA | 284434 |
rs546566758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16764264 | GTGCATAGAGTGAAA[A/G]CCCCTGCCTTATCAT | 284434 |
rs546626324 | snp | G/T | 0 | 0 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749344 | TCACATCACTGACAT[G/T]CACCCAGGGGTCCTC | 284434 |
rs546627623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16785015 | ATGGATATGAAATGT[C/T]CAGAACAGACTAATC | 284434 |
rs546678101 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16726687 | CAAGTGATCCACCCA[A/C]CTCGGCCTCCCAAAG | 284434 |
rs546683063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16761192 | GTAGCAGGGATCAGT[A/G]CTTCCTTCCTTTTCA | 284434 |
rs546688028 | in-del | -/CAAAAA | 0.00438332 | 0.0466095 | intron-variant | NWD1 | GRCh38.p7 | 19:16762553 | AGAGAAACTCTGTCT[-/CAAAAA]CAAACAAACAAACAA | 284434 |
rs546692567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16791767 | TGCCCAGGCTGGAGT[A/G]CAATGGTGTAATCTC | 284434 |
rs546743946 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16766554 | AGGATGTTCTGTTTG[A/G]TTTTGTTTTAATTAT | 284434 |
rs546765153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748436 | GTGATAGTAACTCCA[C/T]GTTTCACTTTTTGAG | 284434 |
rs546793008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16780408 | TGATCCACCCACCTC[A/G]TCCTCCCAAAGTGCT | 284434 |
rs546802405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16810316 | GGTGGTATGTGCCTG[C/T]AATCCCGGCTACCCG | 284434 |
rs546912252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16755803 | TTGGCCTCCCAAAGT[A/G]CTGGGATTACAGGCG | 284434 |
rs546966044 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16782804 | AGCCTGGGCAACAGA[C/G]TGAGATCCTGTCTTT | 284434 |
rs546985143 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16762228 | CTTTTTGCACTCGAA[A/C]TGTCCTCCCGACCTA | 284434 |
rs546995511 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748844 | TAATAATAATAAGAA[G/T]AAGAATAAGAGTAAT | 284434 |
rs547014319 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16733025 | CCAGGAGTTTGATAC[C/T]GGTCTGGGTAATATA | 284434 |
rs547029977 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16782124 | AAAAAAAAAAAGAAT[C/G]TAATCTAACCCTTTT | 284434 |
rs547046047 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16754513 | ATCCATCCATCATCT[C/G]TATCTTCCATTCATC | 284434 |
rs547074267 | snp | C/T | 6.72201e-05 | 0.00579703 | intron-variant | NWD1 | GRCh38.p7 | 19:16797922 | CTTCATCCTCACCTC[C/T]ACCTCGGGAACAGAC | 284434 |
rs547136071 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16731707 | CCTCCAGGGTTCAAG[C/T]GATTCTCTCGCCTCA | 284434 |
rs547182829 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817822 | TTGAGACCAATTAAG[A/G]TTTCACCTACAAATT | 284434 |
rs547196404 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16755524 | CTCTCAAGTAGCTGG[A/G]ATTACAGGCGTGCAC | 284434 |
rs547241094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16776442 | GCGTTGTAGCGGACA[C/T]CTGTAATCCCAGCTA | 284434 |
rs547242496 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NWD1 | GRCh38.p7 | 19:16737965 | GCAAGACTCTATCTC[A/G]AAAAGAAAAGAAAAG | 284434 |
rs547246069 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16729460 | CCCGTCTTCAGGGAG[A/C]CCTTCTCTGCCCCTC | 284434 |
rs547261719 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16774404 | TTTCCATCCATCTAT[-/C]CCCCATCTCTAAATC | 284434 |
rs547266705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16770266 | CATGCTGTTCTCCTG[A/G]TACTGAGTAAGCTCT | 284434 |
rs547304848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16783526 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 284434 |
rs547313811 | snp | G/T | 3.32143e-05 | 0.00407505 | missense | NWD1 | GRCh38.p7 | 19:16815028 | TCTTCACCCTTACAG[G/T]CACCCTGCTGACAGT | 284434 |
rs547378696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16741622 | GATCCACCTGCCTCG[A/G]CCTCCCAAAGTGCTG | 284434 |
rs547424504 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NWD1 | GRCh38.p7 | 19:16781806 | TTTAGAAAGAATCTA[A/G]TCTAGGCCAGGTGCA | 284434 |
rs547439401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16741027 | TAGCCAGCTGTGGTC[A/G]TGGGTGCCTATAATC | 284434 |
rs547482953 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16739921 | ACCACCTGTTTCCTT[C/T]ATATAACCTCTGGTC | 284434 |
rs547516223 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16750594 | GAGTAGCTGGGACTA[C/T]GGGCATGCACCACTG | 284434 |
rs547562627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16763436 | CCTAACCTGACTTGT[A/G]TAATTCAGTCCTCCC | 284434 |
rs547572895 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16732567 | GTAGGAGCCCCTAAT[G/T]CTGTCTCCTTGTACC | 284434 |
rs547592950 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16773893 | TCCATTCATCTATCC[A/C]TCCATCCACCAGCCT | 284434 |
rs547601507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16728775 | CAGTGAAACCCTGTC[C/T]CTACTAAAAATACAA | 284434 |
rs547645737 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16814282 | GGCAGACTTGCCTAA[G/T]GTCACACAGTGAGTA | 284434 |
rs547646681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16797594 | CTCGAGTGATCTGCC[C/T]GCCTTGGCGTCCCAA | 284434 |
rs547651333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16756742 | CGGTACTGCTCCGTG[A/G]CCTGTTAGGAACCAG | 284434 |
rs547713105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16734177 | CACCCTCCTTTGCAA[A/G]GAAAGCTTTGTGAAC | 284434 |
rs547720746 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16722531 | TGACCTCAGGCGATC[C/T]GCCCACCTTGGCCTC | 284434 |
rs547758581 | snp | A/G | 0.000138591 | 0.00832322 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16731256 | GCCAGACCTTCTGCC[A/G]GAGGCACGGCTTGAT | 284434 |
rs547784549 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16772315 | GGCTGCAGTGAGCTG[C/T]GATCGTGCCACTGCA | 284434 |
rs547784677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16728002 | GGAGGCAGAGGTTGC[A/G]GTGAGCCAAGATCGC | 284434 |
rs547805856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16733118 | CCCAGCTACTGGGGA[A/G]GCTGAGGTGGGAGGA | 284434 |
rs547809134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16812629 | AGCTGAGATCACACC[A/G]CTGCACTCCAGCCTG | 284434 |
rs547825566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16774474 | TGTTCCATCCATCCA[C/T]CCATCCACCCATCCA | 284434 |
rs547869039 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16811781 | CATCCCCCTGTGGGG[C/T]GCTTCAAAGCCTGGT | 284434 |
rs547916636 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16809796 | TCTCCTGACCTCGTG[A/T]TCCGCCCACCTTGGC | 284434 |
rs547930883 | snp | G/T | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16771517 | GGAATTTAAGGCAAC[G/T]GGAAAGAAAAATAAC | 284434 |
rs547933723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16794980 | ACAGACGGAGTTTCA[C/T]CATGTTGGCCAGGCT | 284434 |
rs547954214 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816419 | TGGCAGTAAAACAAT[A/C]AACATGTTATAGTTC | 284434 |
rs547955659 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16786062 | TAGAAACAAGGTTTT[G/T]CCATGTTGGCCAGGC | 284434 |
rs548049856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16760649 | AGGCTAGAGTGCAGC[A/G]GCACAATCTTGGCTC | 284434 |
rs548065403 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16774811 | CCTCTACCCACTTAT[C/T]CTTCCATTTTCTTCA | 284434 |
rs548065944 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16792339 | TTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 284434 |
rs548101014 | snp | A/G | 6.7769e-05 | 0.00582065 | missense, upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749172 | AGCGGAGCCTGCTGA[A/G]CTCAGAGGACCGGGA | 284434 |
rs548117164 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16722148 | AACAACAACTAAAAA[A/T]CTAGCTAGGCATGGT | 284434 |
rs548123092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16807433 | AGGAGGTGGAGGTTA[C/T]GGTGACCTGAGATCG | 284434 |
rs548159806 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16772263 | CCAGCTAATATAGAG[A/G]CTGTGGCCGGAAGAT | 284434 |
rs548160345 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718917 | GCAAGCTCCACCTCC[C/T]GGGTTCATGCCATTC | 284434 |
rs548195666 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16719928 | CAGGGGCTTGTCTTC[C/T]GGGTGGCGCCGAGGC | 284434 |
rs548202957 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16802605 | ACCAGAAGCAGAAGC[G/T]GGCACCATGCTTCCT | 284434 |
rs548206511 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817244 | GGCGGAGGTTGCAGT[A/G]AGCTGAGATTGTGCC | 284434 |
rs548289044 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16808995 | GGGCTGAGGCGGAAG[C/G]ATTGATTGAGCCCGG | 284434 |
rs548290955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16802009 | TAAAAATAATGGCCG[A/G]GCATGGTGGCTCACG | 284434 |
rs548333403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16735594 | AGCATTTTGGGAAGC[C/T]GAGGTGGGTGGATCA | 284434 |
rs548391201 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16798519 | AGGAATCTGAGGTGG[A/G]AGGATCACATGAGCC | 284434 |
rs548401189 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16734975 | TGCTACATTGCCCAA[C/T]CTGGTCTTGAACTCC | 284434 |
rs548421170 | snp | A/T | 1.64863e-05 | 0.00287104 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16763866 | CTCACATACGGTTGC[A/T]AACCTGCGGAAGCTG | 284434 |
rs548452765 | snp | C/G/T | 0.00358891 | 0.0422285 | intron-variant | NWD1 | GRCh38.p7 | 19:16798014 | AAATAGGTGAGTTCA[C/G/T]TGGGAGGATATGGGG | 284434 |
rs548465709 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16762445 | GGGATTACAGGCACC[C/T]GCCACCATGCCTGGC | 284434 |
rs548489252 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16737322 | AGGCTAGAGTGCAGT[G/T]GCAAGATCATGGCTC | 284434 |
rs548514304 | snp | C/T | 6.59511e-05 | 0.00574206 | missense, stop-gained | NWD1 | GRCh38.p7 | 19:16797768 | TATTCTTGGCGGACT[C/T]GAGGGGCTTTCGCCG | 284434 |
rs548526933 | snp | C/G | | | missense | NWD1 | GRCh38.p7 | 19:16759226 | GGTCCTCCCTTCAGA[C/G]ACGGTCTCTCGGAGG | 284434 |
rs548554592 | snp | C/T | 0.000161837 | 0.008994 | synonymous-codon, intron-variant | NWD1 | GRCh38.p7 | 19:16794525 | GAGGTTCCTGGTGGT[C/T]TCTGAAGATGAGTCC | 284434 |
rs548574992 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16806933 | GAGGTGGGAGAATTG[C/T]TGGAATCTGGGAGGC | 284434 |
rs548605546 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16759078 | CTAACCGTGCTTGGT[A/C]CCTTGTGGGCGCTGT | 284434 |
rs548609808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16752300 | TGGTGGTCAACCCAA[C/T]GAGGAGGTCTTTCTG | 284434 |
rs548610991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16724470 | GATGCCAAGGTATAC[A/G]CGTGTTCTCTCTGCC | 284434 |
rs548642372 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787207 | TCATAGCTCACTCCA[C/G]CCTCAACCTCCTGCG | 284434 |
rs548654037 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16757909 | ATACAAAAATTAGCC[A/G]GGCGTGGTGGTGCAC | 284434 |
rs548668824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16758546 | CCTCCCAAAGTGCAG[A/G]GATTACAGGTGTGAG | 284434 |
rs548672126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16779884 | CAAGTGATCCTCCCT[C/T]CTTAGCCTACCAAGT | 284434 |
rs548731607 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815940 | GATGAGGAAACTGAG[C/T]CTTGCGGAAGTAGTT | 284434 |
rs548749046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16793847 | CTCCCAAAGTGCTGG[A/G]ATTACAAGCATGAGC | 284434 |
rs548771516 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16762255 | CCTACTTCTCCTTTC[C/T]GCACAGAGGGCAAGA | 284434 |
rs548785377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748258 | CAAAGTGCTGGGATT[A/G]CAGGCATGAGACCCC | 284434 |
rs548797303 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16777661 | GGGAAGGGAAAGGGG[A/C]GAGCAGGGGAAAAAG | 284434 |
rs548816678 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16769355 | TAATCCCAGTTACTC[A/G/T]GGAGGCTGAGGCAGG | 284434 |
rs548878275 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16728865 | AAGAGAATGGCGTGA[A/T]CCCAGGAGGCGGAGC | 284434 |
rs548904238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16781831 | GGTGCAGTGGCTCAC[A/G]CTTGTAATCTCAGCA | 284434 |
rs548941533 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16752880 | GGCTCACACCTGTAG[A/T]CCCAGCTACTCGGGA | 284434 |
rs548967938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16788421 | AAAAATAGAAAAAAT[C/T]AGCCAGGCATGGCGG | 284434 |
rs549030906 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NWD1 | GRCh38.p7 | 19:16723172 | CCAAGTAGCTAGGAC[C/T]GCAGACACGAATCAC | 284434 |
rs549075680 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817936 | AATGCCTTTTTACTA[A/T]TAAAATGCTACAACA | 284434 |
rs549080762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16756006 | GTAACATAAATGGTC[A/G]ACGAACATGTATTTC | 284434 |
rs549106650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16761817 | AGGAAAAAAAAAACA[C/T]GGACCAATTTAGAGA | 284434 |
rs549107994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16755174 | TATATCTATCTCTCT[A/G]TTTCTCATCTATATC | 284434 |
rs549186443 | in-del | -/AAT | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748824 | GTGAGACCCTGTCTC[-/AAT]AATAATAATAATAAG | 284434 |
rs549212608 | in-del | -/TGTTTTGTTTTGTTT | 0.0150606 | 0.0854603 | intron-variant | NWD1 | GRCh38.p7 | 19:16723677 | TTTTACAGCTTTTTC[-/TGTTTTGTTTTGTTT]TGTTTTGTTTTGTTT | 284434 |
rs549219039 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16751180 | CGTGAGCCGAGATCA[C/T]GCCATTGCACTCCAG | 284434 |
rs549236729 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16773658 | AGGAACTGATGCCTG[A/G]CAGTCCTCTGAGAAG | 284434 |
rs549241745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16745714 | CACTGCACTCCAGCC[A/G]GGGTTACAGAGAGAG | 284434 |
rs549310537 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16742626 | GACCAGAACTAGAAT[A/G]GAGAACCACCACAAG | 284434 |
rs549342239 | snp | A/G | 3.32867e-05 | 0.00407949 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750100 | GGTGCTCCTGGACCC[A/G]GAGGCCTACTGGGAG | 284434 |
rs549353145 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16784485 | GTGGATTTTGGTATC[C/T]GCAGGGGTGAAGGAA | 284434 |
rs549354626 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16737991 | AAAAGAAAAGAAAAG[A/C]AAAGAAAAGAAAAGA | 284434 |
rs549360993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16776522 | GCAGTGAGCGGAGAT[C/T]GTTCCACTGCACTCC | 284434 |
rs549380452 | snp | A/C | 0.000140875 | 0.00839152 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744479 | GGATCGATGAGAAGG[A/C]GTGGGAGGTATTGAG | 284434 |
rs549457028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16747115 | GATCTCAGCTCACTC[C/T]AACCTCTGCTTCCCA | 284434 |
rs549480821 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16792791 | CTGAGGCAGGAGAAT[A/C]ACTTGAACCCGGGAG | 284434 |
rs549487570 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16797228 | AGTCAGGCCCTCCCC[C/T]AACCAGCTGTGGGCT | 284434 |
rs549509288 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16805991 | CTCCTGCCTCAGCCT[C/G]CCTTCCAAGTAGCTG | 284434 |
rs549541011 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16742353 | GCACTCCAGCCTGGG[C/T]GACAGAGGGAGATTC | 284434 |
rs549595313 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16811714 | TCTATGGAGGTGTGC[C/T]TGGGTTGGGGTAGTA | 284434 |
rs549629639 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16732391 | CTGTCTGTTGTTGTT[C/G]CTGCTGTTTTTGTCT | 284434 |
rs549631220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16790084 | TCCACTGTGTTATTC[C/T]ATTACATCAATCATA | 284434 |
rs549634461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16770839 | GTCATCTGCAAAATG[C/T]GCAATTGAACTAAAA | 284434 |
rs549665841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16802970 | AAAAAAAAAAAGACA[C/T]ACCTGAGACTGGGTA | 284434 |
rs549674442 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16792229 | GGTGGTTGGTGGACG[A/G]CTGCTTTCATGGACA | 284434 |
rs549702020 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16777027 | AGGGAAGGAACTGGA[A/G]GGAAGGGAAAGGGAA | 284434 |
rs549717058 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | NWD1 | GRCh38.p7 | 19:16764377 | TCCATCCATCCATCC[A/G]TCCATCCATCCATCC | 284434 |
rs549784985 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16808540 | GACTACAGACACTCC[A/G]TTTAAAAAAAAAAGA | 284434 |
rs549798583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16728075 | CAAGAAACAAAATAA[A/G]CCAAAAACTCAAAAA | 284434 |
rs549838664 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16741849 | GGCCCGGTGGCTCCT[G/T]CCTGTAATCCCAGAA | 284434 |
rs549839333 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16801379 | GGGAAGTTGAGGCTA[C/T]AGTGAGTCATGATCG | 284434 |
rs549843076 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16771375 | AAATTGCTTGAACCC[A/G]GGAGGCAGATGTTGC | 284434 |
rs549867357 | snp | C/T | 0.0640965 | 0.167152 | intron-variant | NWD1 | GRCh38.p7 | 19:16782869 | CCTTTTCCTTCTTTC[C/T]TTCTTTCTTTCTTTC | 284434 |
rs549925503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16774941 | CCATCTACCCATCTA[C/T]CTGCCCATCCATTCA | 284434 |
rs549980342 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16751272 | TCATGATAGTCTGGG[A/G]CCATTGCTCAGAGAT | 284434 |
rs550023419 | snp | A/G | 1.65767e-05 | 0.00287891 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16763935 | GGAGGAGCTGAAACA[A/G]GAGGTTCTGGGTAAG | 284434 |
rs550031651 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16808378 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 284434 |
rs550045947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16735398 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 284434 |
rs550088950 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16807216 | TATGAACACCAGGCC[A/G]GGTGTGGTGGCTCAC | 284434 |
rs550121442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16722647 | GTCCATACCCCACAC[A/G]TTAAAGCTGTAGCTC | 284434 |
rs550139383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16726596 | AGGCCTGCGCCACCA[C/T]ACCTGGCTAATTTTT | 284434 |
rs550191152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16807466 | CTATTGCACTACAGC[C/T]TGGGCAACAGAGTGA | 284434 |
rs550200743 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16725919 | GCTGGGACAACAGGC[A/T]GGCACCATCATGCCA | 284434 |
rs550207914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16769647 | AAACATCCAAGCTTG[C/T]GTGCCGGGGGCCCTG | 284434 |
rs550218845 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751676 | CATGGTGGCGGTCAC[C/T]TGTAATCCCAGCTGC | 284434 |
rs550229831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16813299 | GGAGCCCAAGAATTC[C/T]CAATCTGTTTCCAGG | 284434 |
rs550239426 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16788364 | GCTTGAGGCCAGGAG[C/T]TCAAGGCCAGCCTCG | 284434 |
rs550267245 | in-del | -/ATCC | 0.0019579 | 0.0312269 | intron-variant | NWD1 | GRCh38.p7 | 19:16754030 | ATCTTCCATCTATCC[-/ATCC]ATCCATCCATCCATC | 284434 |
rs550267371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16768953 | AGTGCTGCTGTCTCT[C/T]CTCCAGACAGCATCC | 284434 |
rs550284272 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16720358 | TTAAGGGGTCACTAC[C/G]CAATGGGATGGTCAG | 284434 |
rs550316042 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16760694 | CTCCCAGGTTTCAGC[G/T]ATTCTCCTGCCTTAG | 284434 |
rs550330150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16775004 | CCCACTCATTTACCT[C/T]CATTCACCCATCTAT | 284434 |
rs550349173 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16804519 | AGGATTGCTTGAGCC[A/G]TGGAGTTCAAGGCTG | 284434 |
rs550376464 | snp | A/C/G | 0.00181808 | 0.030098 | synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749278 | GGTGGACCGGCTCGC[A/C/G]GATGGCTGCCTGGAC | 284434 |
rs550385733 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16810269 | ATGGTGAAACCCTGT[C/T]TCTACTAAAAATACA | 284434 |
rs550444323 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16795467 | TATTGCGTAGGCTGT[A/G]GTGCAGTGGTATGAT | 284434 |
rs550445197 | snp | C/T | 0.00081042 | 0.0201135 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815367 | TGTGGGGGTATGGGG[C/T]TCCAGTGAGTTAGCC | 284434 |
rs550449578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16754601 | TTCCATCCATCATCT[A/G]TCTTCCTTTTATCCA | 284434 |
rs550496952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16757174 | CCCTACCCTGGTCCG[C/T]GGGAAAAAAATTGTC | 284434 |
rs550507236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16805314 | TCCACCTGCCTCGGC[C/T]TCCCAAAGTGCTAGG | 284434 |
rs550512845 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16801446 | CCTGTCTCTAAAAAC[A/C]AACAAAAAAGCCAGG | 284434 |
rs550607034 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16766388 | GCCTGGGTGACAGAG[C/T]GAGACCCTGTCTCAA | 284434 |
rs550649322 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16754706 | CCATCATCTCTAGCA[A/T]CCATCCATCCATCCA | 284434 |
rs550667329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16796992 | GAGACCAGCTTGGCC[A/G]GCATGGTGAAACCTG | 284434 |
rs550670756 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16765745 | CAGGTAGGGCTGGGC[A/G]CAGTGGCTCACACCT | 284434 |
rs550673859 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16757918 | TTAGCCGGGCGTGGT[C/G]GTGCACACCTGTAGT | 284434 |
rs550730487 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16730863 | AGGAGACTCCACAAA[A/G]TAAATAAAATAACTG | 284434 |
rs550731770 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16772377 | CTCTAAAAAAATAAA[C/T]AGCCAGGCGCGGTGG | 284434 |
rs550767745 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816660 | TCTCAGTCTTCTCAG[A/G]CTTTTACTTTAATGC | 284434 |
rs550776831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16793618 | GTCTTGCTCTGTCGC[C/T]CAGACTGGAATGCAG | 284434 |
rs550837459 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16792912 | AAAGGAATCATGGTG[G/T]TGCATACTTGTACTC | 284434 |
rs550862389 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16743361 | GACTACAGATGCACA[C/G]CCCCACACCCTGATA | 284434 |
rs550899050 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16798664 | AAGTCTCACTCAGTC[A/G]CCCAGGCTGGAGGGC | 284434 |
rs550901212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16761101 | GGCATTTCAGATCAA[C/T]GAAATCTCACACTAT | 284434 |
rs550959226 | in-del | -/TTTC | 0.0189856 | 0.0955633 | intron-variant | NWD1 | GRCh38.p7 | 19:16762298 | GTCCCCCCCACTCCT[-/TTTC]TTTTTTTTTTTTTTT | 284434 |
rs551006405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16794903 | CCTCCCACGTCAGCT[C/T]CCTGAATAGCTGGGA | 284434 |
rs551006467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16787956 | ATCATAGGCCAGGCG[C/T]GGCGGCTCATGCCTG | 284434 |
rs551012377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16784884 | CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA | 284434 |
rs551038278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16759698 | CCTGGGCAACGTAGC[A/G]AGGCCCCATCTCTAC | 284434 |
rs551052722 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16738050 | GCTATAGCCTGAAAG[G/T]CAAGTGTGGCCTGCT | 284434 |
rs551065697 | snp | A/C/G | 8.8849e-05 | 0.00666468 | missense, intron-variant | NWD1 | GRCh38.p7 | 19:16794553 | TCCCTCCTCGCCGCA[A/C/G]GTAGCGTTTAGCTCT | 284434 |
rs551104474 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16750487 | GAGATGGAGGTCTGG[C/G]TATGTCACCCAGGCT | 284434 |
rs551105400 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16759879 | CGTGCCTGTAATCCC[A/G]GCTGCTCGGGAGGCT | 284434 |
rs551129242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16728248 | TTTGTTTTGGAGAAC[A/G]GAGTATTATGGAACA | 284434 |
rs551213033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16785564 | AATTTAAAAAATTAA[C/T]GTGATAAAGAAAAAA | 284434 |
rs551277783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16775737 | GCAGTGGCGCAATCT[C/T]GGCTCACTGCACCTC | 284434 |
rs551339514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16782591 | GCCCTAAAAGGCTCA[A/G]TTGACAAGATACATA | 284434 |
rs551358885 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16773764 | TGTCATTCATTTTTT[G/T]CTTCCTTCCATTCAT | 284434 |
rs551449101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16726717 | GTGCTGGGATTATAG[A/G]TGTGAGCCACTGCAC | 284434 |
rs551452951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | NWD1 | GRCh38.p7 | 19:16745067 | GTTTAATGGACTCAC[A/G]ATTCCACATGGCTGG | 284434 |
rs551578646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16733750 | TTAATGCCCATGCCC[A/G]TCCTCTGACGCGGAT | 284434 |
rs551588187 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16731585 | GCTGGGATTACAGGC[A/G]TGAGCCACTGAGCCC | 284434 |
rs551591458 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754345 | ACCCATTGTTTCTAT[C/G]TTCTTTCCATCCATC | 284434 |
rs551593064 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16768971 | CCAGACAGCATCCTC[A/G]GAGGTCTGCCTACTT | 284434 |
rs551600056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16780036 | TCTGCAGTCAGTCAG[C/T]GGATTATCTAGGAGC | 284434 |
rs551604489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16775074 | CCACTGAGTTCACTT[A/G]TGGTTCAAATGTCAG | 284434 |
rs551628474 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16741473 | TGGGTTCAAGCAATT[C/G]TCCTTCCTCAGCCTC | 284434 |
rs551630922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16768070 | GATCTCAGCTCACCG[C/T]AACCTCCACCTCCTG | 284434 |
rs551689415 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16740924 | AGCACTTTGAGAGGC[C/T]GAGGCAGGCGGATCA | 284434 |
rs551693800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16767506 | TGTAGTTCCAGCTAC[C/T]TGAGAGGCTGAGGTG | 284434 |
rs551719710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16732469 | TATAAGAGGGCTTTG[C/T]GATATGGGGGATGGG | 284434 |
rs551761058 | snp | C/G | 0.00123083 | 0.024777 | intron-variant | NWD1 | GRCh38.p7 | 19:16761947 | GCTTGATGGGTCACC[C/G]AGGTCTATCAGTCTG | 284434 |
rs551771477 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16811811 | TTCTGAGGTCAGGAG[G/T]TTGGGACCAGCCTGG | 284434 |
rs551828328 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16795666 | AGGTTATCTGCCTGC[A/G]TCTGCCTCCCAAAGT | 284434 |
rs551854415 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16730171 | TACTAAAACACAAAA[A/C]ATTAGCCAGGTGTGG | 284434 |
rs551874683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16771022 | GAGGGAGATGGGGCC[A/G]AGTGCGGGGGTTCAC | 284434 |
rs551918275 | snp | C/T | 3.29669e-05 | 0.00405984 | synonymous-codon, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800035 | TCTCAGCGATGCTCA[C/T]AGGTCCCGGGTGCCT | 284434 |
rs551925370 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16786738 | TTTTAGTAGAGACGG[C/G]GTTTTGCCTTGTTGG | 284434 |
rs551940434 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | NWD1 | GRCh38.p7 | 19:16777594 | GGGGAGGGGAGGGGA[A/T]AGTGGAGGGGAGGGG | 284434 |
rs552018804 | snp | A/C | 1.6519e-05 | 0.00287388 | missense | NWD1 | GRCh38.p7 | 19:16765114 | GACCTGTGTGCCCCT[A/C]ACCTGGACTCCCCTG | 284434 |
rs552082838 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16769515 | TGAATCTTCTAGATG[G/T]TTCTCCCATTGTCCT | 284434 |
rs552103239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16727224 | GCTATGGTGACTACT[A/G]CGCTCTGAGGACGAG | 284434 |
rs552136223 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16803568 | ACATAGGAATTTGTC[A/T]GGGGGACACAAATCT | 284434 |
rs552158278 | in-del | -/A | 0.0166325 | 0.0896639 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817522 | CAGGAGAATGGCTTG[-/A]ACCCGGGAGGCGGAG | 284434 |
rs552176960 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16809196 | TCAAGCAACTCTCCC[A/G]CCTCGGCCTCCCAAG | 284434 |
rs552196107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16723380 | ATTTTTAAATTTTTT[A/G]TAGAAATGGGGTTTC | 284434 |
rs552211661 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815829 | ACTGATGTGGACCAC[A/G]GAACCTCACAGTTTA | 284434 |
rs552242981 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16801822 | GTGGATAGATTAATG[C/T]CCTCTCCTGGCAAGG | 284434 |
rs552296282 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16775228 | ACTAGAATGCTGTGT[C/T]GAGGATTCTAAGACT | 284434 |
rs552304803 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | NWD1 | GRCh38.p7 | 19:16742391 | AAAAAATAAAATAAA[A/T]AATAAATAAATAAAT | 284434 |
rs552318138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16808973 | ACCTGTGATCCAGCT[A/G]CTTGGAGGGCTGAGG | 284434 |
rs552322913 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754728 | ATCCATCCATCATCT[C/G]TATCTTCCTTCCATC | 284434 |
rs552367859 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16747237 | AGACGGGGTTTCCCC[A/G]TGTTGCTCAGGCTGG | 284434 |
rs552396258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16728740 | ACGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 284434 |
rs552406545 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16801393 | ACAGTGAGTCATGAT[C/T]GCACTACTGCACTCC | 284434 |
rs552443957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16725139 | ATGCCTCAGCCTCTC[A/G]AATAGCTGGGACTAC | 284434 |
rs552446677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16730612 | ATCCCAGCTACTCAG[A/G]AGGCTGAGGTGGGAG | 284434 |
rs552452590 | in-del | -/TCTT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16783003 | CCTCCTTTCTCTCTC[-/TCTT]TCTTTCTTTCCTTCT | 284434 |
rs552462030 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16779654 | ATTTCTTTTTCTTTT[C/T]AAATATGGGATCTCA | 284434 |
rs552466467 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718465 | GGCATGAGCCACCGC[A/G]CCTGACCAAGTATCT | 284434 |
rs552494025 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16760835 | CCTCAGGTGATCTGC[A/C]CGCCTTGGCCTCCCA | 284434 |
rs552504255 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16724635 | GGAGGATCGTTTGTT[G/T]GCAGGAGCCTGCCAA | 284434 |
rs552516881 | in-del | -/CTTTC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16780619 | CTTCTTTTCTTTTCT[-/CTTTC]CTTTCCTTTCCTTTC | 284434 |
rs552588122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16801545 | AGTTTGAGACCAGAC[A/G]TCTCTACATAAAAGA | 284434 |
rs552620100 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16776436 | AGCCGGGCGTTGTAG[C/T]GGACACCTGTAATCC | 284434 |
rs552655108 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16720458 | CACTAAAGTACAGGA[C/G]GTGCAAAGGCCCTGA | 284434 |
rs552659980 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16763499 | TTTGCCCATGCTGTT[C/G]CCTTGCCCTGGAATG | 284434 |
rs552668204 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16763415 | TCTCATTTCCCACCC[A/G]CATCCCCTAACCTGA | 284434 |
rs552755579 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16788758 | TTCTGTTATTAGGCA[C/T]ACAAGCGTGAGAACT | 284434 |
rs552764137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748592 | AGCACTTTGGGAGGC[C/T]GAGGTTGAATTGCTT | 284434 |
rs552773383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16738442 | GACGTGGTGGCACAT[A/G]CCTGTGATCCCAGCT | 284434 |
rs552784801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16783626 | GCAAAAAGAGCAAAA[C/T]TCCATCTCAAAAAAT | 284434 |
rs552804719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16791968 | ATCTGCCCACCTCGG[C/T]CTCCCAGAGTACTGG | 284434 |
rs552832669 | snp | C/T | 0.000330961 | 0.0128597 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744644 | CCTTAACTTCTGTCC[C/T]ACGCTCTGGAGCCCA | 284434 |
rs552834516 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16737726 | CACCTGTAATCCCAG[A/C]ACTTTGGGAGGCCAA | 284434 |
rs552898214 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16744198 | GTTCAATACCAGCCC[A/G]GGTAATGTAGTGAGA | 284434 |
rs552912547 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16809407 | GCAATATTTTTAAAA[A/G]TCTAAAATGAATACC | 284434 |
rs552933469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16772957 | TCTGAAGCAAGGGTA[A/G]GTGTGTCTGGAGAGC | 284434 |
rs552943029 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749048 | GAACCAATGCACATC[C/G]CCCAACAACAGGTCT | 284434 |
rs552980851 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817593 | AGTGACAGAGACTCT[A/G]TCTCCAAAAAAAAAA | 284434 |
rs552998098 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16754824 | TCCATCCATCCACAC[A/T]TCATCTCTATCTTCC | 284434 |
rs553040901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16765972 | CAGTGAGCCGAGATC[A/G]CACCACTGCACTCCA | 284434 |
rs553051457 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16784572 | TGAGAGGGGAATGAG[G/T]TTGGCGGGTCTACAG | 284434 |
rs553052382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16730372 | AAAATCTATTTATGT[A/G]TTTATTTATTGTGCC | 284434 |
rs553072631 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | NWD1 | GRCh38.p7 | 19:16771232 | CGAGGCAGGCAGATT[G/T]CTTGAGGCCAGGAGT | 284434 |
rs553095237 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815993 | TCCAAGGTGCAAGAG[C/T]TCTGAGAGTGAGCCT | 284434 |
rs553096890 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16810267 | ACATGGTGAAACCCT[-/G]TCTCTACTAAAAATA | 284434 |
rs553121396 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16720033 | GAGAGGCTGGAGCCC[C/T]CAGGACAGCCAGAAC | 284434 |
rs553130536 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16760763 | ACCCAGCTAATTTTT[C/G]TATTTTTAGTAGAGA | 284434 |
rs553131764 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | NWD1 | GRCh38.p7 | 19:16778113 | AGGTGGAAACAAAAT[G/T]CTGTATTCTCAGAGC | 284434 |
rs553166945 | in-del | -/ATC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787908 | ATAATAATAATAATC[-/ATC]ATCATCATCATCATC | 284434 |
rs553227620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16809851 | CATGAGCCACCGTGC[C/T]TGGCTGCTCCGTGCT | 284434 |
rs553229565 | in-del | -/GGA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16761630 | GCCTCCCAAAGTGCT[-/GGA]GGGATCACAGGCATG | 284434 |
rs553242919 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16780107 | TGCTCCACGTGGTCT[A/G]TCATCATTCAGCGTC | 284434 |
rs553266612 | snp | C/T | 0.00125134 | 0.0249821 | missense | NWD1 | GRCh38.p7 | 19:16797816 | TGGAACATGAAGACA[C/T]GGTGGAGACGGCTGT | 284434 |
rs553296465 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816739 | AATTCCTGATAGAGT[C/G]TCAATAAAAGCAACC | 284434 |
rs553306239 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16779664 | CTTTTTAAATATGGG[A/C]TCTCACTGTATTGCC | 284434 |
rs553374329 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16808720 | TCCAGTGATCCTCCC[A/G]CCTCAGCCTCCCAAA | 284434 |
rs553426146 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16735932 | TTGCGCCACTGCACT[C/T]TAGCCTGGGTGACAT | 284434 |
rs553434270 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16738541 | GCCACTGCATTCCAG[A/G]CTGCGCAACAGACGG | 284434 |
rs553453518 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16813609 | AGCCTCCTGAGTAGC[C/T]GGGATTACGGGCGCC | 284434 |
rs553503360 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16801607 | TGTAGTCCAAGCTAC[G/T]TGGGAGGCTGTGGTG | 284434 |
rs553528272 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16737566 | TGGTCTAGTTTTAAG[-/T]TTTTTTTTTTTTTTT | 284434 |
rs553566017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16725503 | AAACCTCCTGCAGGC[A/G]AAGATAACTAGCTAG | 284434 |
rs553627072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16730982 | GGCGCAGTGGCTCAC[A/G]CCTGTAATCCCAACA | 284434 |
rs553647504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16771927 | CAGCCTCCCGAGTAG[C/G]TGGGATTACAGGCCT | 284434 |
rs553710670 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | NWD1 | GRCh38.p7 | 19:16730981 | AGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAAC | 284434 |
rs553725172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16768422 | ATTTGTGTGTTTCTA[C/T]CTTTTGGATATTGTG | 284434 |
rs553733489 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16813013 | AGGGCCCACAATCCC[A/T]CTTCTAGACCCATGC | 284434 |
rs553742907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16755523 | CCTCTCAAGTAGCTG[A/G]GATTACAGGCGTGCA | 284434 |
rs553790390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16774624 | CATCCATTCATCAAA[C/T]CACCTTCCCATCCTT | 284434 |
rs553798426 | snp | A/C | | | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744536 | ACCTGGAGCTGGTGG[A/C]ACGATACTTCCAGAG | 284434 |
rs553820905 | snp | A/G | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748198 | CATGTTGGCCAGGCT[A/G]GTCTCAAACTCCTGA | 284434 |
rs553832126 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16730343 | AACTAACAAAAAAAC[-/A]AAAAAAAAAACCCAA | 284434 |
rs553913442 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NWD1 | GRCh38.p7 | 19:16799111 | GTTAAAGGAATGGGA[A/G]GATGTGAAGGCCCTT | 284434 |
rs553931209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16787998 | CTGTGGGAGGCCGAG[A/G]TGGGTAGATCACCTG | 284434 |
rs553954420 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16739610 | CACCCCTCTACTGCC[C/G]AAGAGCCACAGCATC | 284434 |
rs553971158 | snp | A/C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16799609 | CCTCCCGGGTTCAAG[A/C/T]GATTCTCCTGCCTCA | 284434 |
rs553991949 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16787436 | CTGTTTAGTATTCAA[A/C]ATCTGGGGCAACTGA | 284434 |
rs554003475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16757335 | AGCATGCCCTGTGCC[C/T]TCTGGGAGCCTCACT | 284434 |
rs554021338 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16792982 | CTTAGGAGGTGGAGG[A/C]TGCAGTGAGCCAAGA | 284434 |
rs554033422 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16722271 | GCCACTGCACTCCAG[C/G]CTGGGCGACAGAGCA | 284434 |
rs554047365 | in-del | -/ATATATA | 0.0776332 | 0.181079 | intron-variant | NWD1 | GRCh38.p7 | 19:16738776 | ATATAATGATATATA[-/ATATATA]ATATATAATAACATA | 284434 |
rs554081215 | snp | A/G/T | 6.67049e-05 | 0.00577483 | missense | NWD1 | GRCh38.p7 | 19:16750151 | CCAAGGCCAGCAGAT[A/G/T]ATCCAACTCCTGCTG | 284434 |
rs554096517 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790325 | TTAGCACACTGTAAG[A/C]ACCAAATAATTGATA | 284434 |
rs554104547 | snp | C/T | 1.66385e-05 | 0.00288426 | missense | NWD1 | GRCh38.p7 | 19:16807727 | AGGACGTGATATGCA[C/T]TCCCCCTCCCGAGGC | 284434 |
rs554110730 | snp | A/G | 0.139225 | 0.224118 | intron-variant | NWD1 | GRCh38.p7 | 19:16799669 | GCACCACCAAGCCTG[A/G]CTAATTTTTTGTATT | 284434 |
rs554151225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16752685 | TCCCAGATTTCCCGA[C/T]TGGCTTACACTCTAT | 284434 |
rs554157353 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16805389 | TGTAGAGATAAGGTC[C/T]CTCTATCTTGCCCAG | 284434 |
rs554212771 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16758912 | AGGAGACTGAGGCAG[A/G]AGAATCGCTTGAACC | 284434 |
rs554225321 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16796013 | TATTGAGCAACAAAA[C/T]AGCTCTCAGGGGAGA | 284434 |
rs554233850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16726852 | CTGGTCTCCACCCAC[A/G]TGATGCCAGTAGCAT | 284434 |
rs554240091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16721095 | CCTCAAGTAATCTGC[C/T]TGTTTTGGCCTCTCA | 284434 |
rs554243398 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | NWD1 | GRCh38.p7 | 19:16730253 | CTTGAACCCAGGAGG[A/C]AGAGGTTGCAGTGAG | 284434 |
rs554257978 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NWD1 | GRCh38.p7 | 19:16767024 | ACATTCACTCCCTGT[A/G]CTAGTCTGTTTTCAC | 284434 |
rs554283344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16812057 | GGCTCATGCCTGTAA[C/T]CTCAGCACTTCGGGA | 284434 |
rs554285332 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16805565 | TTGAACTCCTGGTCT[C/G]AAGCCATCCTCTCAC | 284434 |
rs554324954 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16778184 | GGAAGAGGCACACAG[A/C]AGGAAAAGGACTTCC | 284434 |
rs554367539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16724302 | GATCTGCTAACACAT[C/T]GCACTACCTCATATA | 284434 |
rs554373026 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16746030 | TAACTTTTGACTCCC[C/T]CAAAACGTAACTACT | 284434 |
rs554460460 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16794191 | GCCCACATGGTGAAA[C/T]CCCATCTCTACTAAA | 284434 |
rs554497792 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16727597 | TACCCGCCGGCGGCT[C/T]CTGCGGGGTGAAGCC | 284434 |
rs554504669 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16775910 | TGACCTCAGGTGATC[C/G]CCTACCTTGGCCTCC | 284434 |
rs554508072 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16747256 | TGCTCAGGCTGGTCT[C/T]GAACTCCTGACCTCT | 284434 |
rs554518644 | in-del | -/CTTC | 0.00438332 | 0.0466095 | intron-variant | NWD1 | GRCh38.p7 | 19:16762782 | TTTTTCCCTCCCTCG[-/CTTC]CTTCCTTCCTTCCTT | 284434 |
rs554575728 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16797227 | AAGTCAGGCCCTCCC[C/T]CAACCAGCTGTGGGC | 284434 |
rs554585413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16724727 | AGACGAAGTTTCGCT[C/T]CTATTGCCCAGGCTG | 284434 |
rs554617294 | in-del | -/AGGGCCTTT | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16741271 | GCTTCTTCCTGCCAC[-/AGGGCCTTT]GCACATGCTGCTCCC | 284434 |
rs554624115 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16758622 | TGGGCCAGGGTGGAG[C/T]GGGGTAGGTGCAGTT | 284434 |
rs554628311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16809234 | GATTACAGATAAGCA[C/T]CACCATGCCCAGCTA | 284434 |
rs554633763 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16733391 | CCAGATGTGGTGACA[C/T]GCACCTGTAATCCCA | 284434 |
rs554641207 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718746 | TGTTAGCCAGGATGG[C/T]CTTGATCTCCTGACC | 284434 |
rs554646140 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732241 | AAAAAAAAAGGCAGA[G/T]GGAGGGGTTACAGCC | 284434 |
rs554653148 | in-del | -/A | 0.0876345 | 0.190099 | intron-variant | NWD1 | GRCh38.p7 | 19:16776774 | CCTCTACAAAAAGTT[-/A]AAAAAAAAAAAAAAA | 284434 |
rs554712627 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16789722 | CCTCTCTCTCTTTTT[A/T]TTTTTTTTTTTTTGA | 284434 |
rs554755075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748517 | GTTGCCTACCCTGAG[A/G]GGTCTTTGATTAATA | 284434 |
rs554762485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16735085 | TTATAAATAAACTTC[C/T]GAATTTGGAATTTAG | 284434 |
rs554767664 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16755209 | CTGTCTATCATTAAT[A/C]TCTCTCTCTCTCTTT | 284434 |
rs554773742 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16770373 | CTTGTGAAGAAGGGC[A/G]TGTTTGCTTCCCCTT | 284434 |
rs554825925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16734506 | CGCCACTGCACTCCA[A/G]CCTGGGTGATAGAGC | 284434 |
rs554826744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16729741 | CAGTGTGGTGGTGTG[C/T]GCCTGTAATCCCAGC | 284434 |
rs554849291 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16805952 | TGACACACTGCAACC[G/T]CCACCTCCTGGGTTC | 284434 |
rs554859707 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16770552 | TGAGCCCCACCGTGT[C/T]CATTGAAATCTTGGC | 284434 |
rs554989375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16783227 | TTTTGTAGAGACTGG[A/G]TCTCACCGTGTTTCC | 284434 |
rs555017127 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16746367 | CCCGTATCAAACAAA[A/C]AAACAAAGAAACAAC | 284434 |
rs555033788 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16724845 | CTACAGGCATGTGAC[A/G]CCATACCCAGCTAAT | 284434 |
rs555055205 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16723009 | GACTGAAATCTCACA[C/G]CTGGTCTCTTCTGGA | 284434 |
rs555076941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16750987 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCGGATCA | 284434 |
rs555108407 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16727464 | TGGCCCTGCCCGGCT[A/G]GCCTACCAGGAAGGC | 284434 |
rs555168633 | snp | A/T | 0.111224 | 0.207945 | intron-variant | NWD1 | GRCh38.p7 | 19:16728960 | AAAAAAAAAAAAAAA[A/T]AAAATAAGTAATTGC | 284434 |
rs555191024 | snp | A/T | 0.0622301 | 0.165053 | intron-variant | NWD1 | GRCh38.p7 | 19:16790646 | TTAAAAAAAAATAAA[A/T]AAATAAATAAATAAA | 284434 |
rs555234311 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16814785 | GGGCCAAAAACCTAC[A/T]CTAAGCACATGACCT | 284434 |
rs555309532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16804053 | AGGTTACCTAGAAGC[C/T]GAATCTGTGATGAGG | 284434 |
rs555324480 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16783830 | CAGACCTTTATTGTC[A/G]TTGTCCCCCAAACAA | 284434 |
rs555335988 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16772627 | CTCCAACCTAGGTGA[C/T]AGGCTAAAATTCCAT | 284434 |
rs555360685 | snp | A/G | 0.000656168 | 0.0181012 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744661 | CGCTCTGGAGCCCAG[A/G]AGGCCCGGAGGCTGG | 284434 |
rs555365878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16739371 | TTATTTTTTTAAGGA[A/G]GAAAGGGAAAAGAAG | 284434 |
rs555368226 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16811463 | GTGGTGCATGCCTGT[A/T]ATCCCAGCTACTTGG | 284434 |
rs555390311 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16800480 | AGACTGCAGTGAGCC[A/G]GGATCCTGACTCTGC | 284434 |
rs555448976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16793163 | TGAGTTCTCAAGGTA[C/T]CAAATACAACAACGA | 284434 |
rs555481976 | snp | C/T | 1.65682e-05 | 0.00287817 | synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749383 | CCGCCTGCCGTGGAG[C/T]CGCGACTTGGTGAAC | 284434 |
rs555482477 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16809885 | TCTTTATCCAACTGA[A/T]ACTTATTGAAAAACC | 284434 |
rs555572193 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816918 | ATGTATGCTTGGATG[C/T]ATTGGGCAGCAGCTT | 284434 |
rs555656151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16721000 | GGATTACAGGTACAT[A/G]CCACCGCGCCAGCTA | 284434 |
rs555718289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16780445 | ACAGGCGTGAGCCAC[C/T]GTGCCCAGCCAAAGG | 284434 |
rs555736819 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817495 | TAATTCCAGCTACTT[A/G]GGAGGCTGAGGCAGG | 284434 |
rs555739993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16769789 | TCCCCGATCCTTGCC[C/T]CTGAATTTTCTATCA | 284434 |
rs555789267 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16761251 | GGACCAGGTTTTGTT[C/T]ATCTTCGTCTATGGA | 284434 |
rs555799519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16769235 | GGGAGGCTGAGGCAG[A/G]CAGATCACTTGAGGT | 284434 |
rs555819266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16760046 | TGTGGTCCCAGCTAC[C/T]TGGGAGGCTGAGGTG | 284434 |
rs555820024 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16731093 | CCACAAAAAAGGGGA[A/C]AAAAGACAAAAGTAA | 284434 |
rs555820123 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | NWD1 | GRCh38.p7 | 19:16737568 | GGTCTAGTTTTAAGT[G/T]TTTTTTTTTTTTTGA | 284434 |
rs555822516 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16719388 | GTGATCCGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 284434 |
rs555874430 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16743792 | GGTTCAAGCAATTCT[C/T]CTGCCTCAGCCTCCC | 284434 |
rs555881453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16736800 | TCCTCCAGGATATGC[C/T]CCCTGCTTTCTAGAC | 284434 |
rs555962218 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16720564 | ATGTCTAGGGAGACT[G/T]TTTTTTTTTTGAGAC | 284434 |
rs555971154 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16795610 | TTAGTAGAGATGGGG[A/T]TTCATCATGTTGGCC | 284434 |
rs555997087 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16760827 | ACTCCTGACCTCAGG[A/T]GATCTGCCCGCCTTG | 284434 |
rs556004407 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16754892 | TTCATCCACCCATCC[A/G]TCATATCTATCTATC | 284434 |
rs556012275 | snp | C/T | 0.000477976 | 0.0154518 | intron-variant | NWD1 | GRCh38.p7 | 19:16812886 | GGCAGGATTGAGCTT[C/T]GATCTGGAGAGAAAA | 284434 |
rs556073343 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764294 | TGAGAGACCCTATCT[G/T]TCTGTCTGTCTATTT | 284434 |
rs556148189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16756803 | ACAAGTGAAGCTTCA[C/T]CTGTATCTACAGCCA | 284434 |
rs556152618 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16793295 | CGGGAGTGCAGTGGC[A/G]CGATCATGGCTCCCT | 284434 |
rs556159798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16728816 | AGGCGTGGTGGCGGG[C/T]GCCTGTAGCCCCAGC | 284434 |
rs556188459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16723454 | TGCTGGGATTACAGG[C/T]GTGAGCCACCAAGTC | 284434 |
rs556211742 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16756235 | TGAGCCTGGGTGACA[C/G]AGCAAGACTCTGCCT | 284434 |
rs556215786 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16772890 | GAGGAAGGAAAGGGA[A/G]GCATTCTAGGCAACC | 284434 |
rs556219419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16763603 | TCAGGAAACATTCCC[C/T]ATTCCTCCCAGAAAG | 284434 |
rs556220464 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16813622 | GCTGGGATTACGGGC[A/G]CCCACCACCACACTC | 284434 |
rs556221019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16728362 | CGATCTGGACTCACT[A/G]TTACCTCTGTCTCCC | 284434 |
rs556231546 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16752869 | CTGGGCGTGGTGGCT[C/T]ACACCTGTAGTCCCA | 284434 |
rs556236323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16727717 | AGAGGCAGGTTGGCA[C/T]GCTCAGGCGGTGTCA | 284434 |
rs556279053 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16770548 | ATTTTGAGCCCCACC[A/G]TGTCCATTGAAATCT | 284434 |
rs556292272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16789854 | TCCTGAATAGCTGGG[A/G]CTACAGGCGCACGCC | 284434 |
rs556300469 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718620 | CCCAGGTTCATGCCA[C/T]TCTCCTGCCTCAGCT | 284434 |
rs556333393 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16758623 | GGGCCAGGGTGGAGT[C/G]GGGTAGGTGCAGTTG | 284434 |
rs556346923 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16804474 | GTGGTACATGCCTGT[A/G]GTCCTAGTTACTCCA | 284434 |
rs556354137 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NWD1 | GRCh38.p7 | 19:16762361 | GAGTGCAATGGCGTG[A/G]TCTCAGCTCACTGCA | 284434 |
rs556368512 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16747662 | ACAGGCATGAACTAC[A/T]CCTGGCCCTCCAAGA | 284434 |
rs556398157 | snp | A/T | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817008 | AAATATTAAAAATAA[A/T]GGCAAAAACTGGCTG | 284434 |
rs556407059 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16755833 | GTGAGCCACCGTACC[C/T]GGCCTATAATCTATC | 284434 |
rs556418892 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16750699 | GGAGTGCAGTGGCAT[A/G]ATCATAGCTCACTGC | 284434 |
rs556480866 | snp | G/T | 0.00063509 | 0.0178085 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750172 | ACTCCTGCTGGCAGC[G/T]GCAAGGAGGACGCTG | 284434 |
rs556536902 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16777499 | AAGGGAAAGGGGAGG[A/G]AAGGGAAGGGGAGGG | 284434 |
rs556567410 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16794654 | GTCCTAGGGCCAGAG[C/G]TTAGCAACGTTTTCT | 284434 |
rs556577640 | in-del | -/GAA | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16751961 | AAGAAAAGAAGAAGG[-/GAA]GAAGAAGAAGAAAAA | 284434 |
rs556589288 | in-del | -/TCCATCCATCCA | 0.00438332 | 0.0466095 | intron-variant | NWD1 | GRCh38.p7 | 19:16754463 | CCATCATCTCTATTT[-/TCCATCCATCCA]TCCATCCATCCATCC | 284434 |
rs556590438 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16731701 | CCTTGGCCTCCAGGG[G/T]TCAAGCGATTCTCTC | 284434 |
rs556622816 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16762998 | CATGTTGGCCAGGCT[C/G]GTCTCGAACTCCTGA | 284434 |
rs556655855 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16793378 | AGCTGGGACTACAGG[C/T]GCATGCCCCCATGCC | 284434 |
rs556689233 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16799722 | CATGTTGGTCAGGCT[G/T]GTCTCGAACTCCTGA | 284434 |
rs556698324 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16809480 | CTGGATCAAATCCTG[C/T]ACTGGCTTAGTGCTG | 284434 |
rs556735788 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16740280 | CTCTGGCCTGGGTGC[C/T]AGAGGAAGAGTCTGT | 284434 |
rs556747373 | snp | C/G/T | 0.000322342 | 0.0126914 | missense | NWD1 | GRCh38.p7 | 19:16773282 | GATTCCTCCAGCCCC[C/G/T]GGGAGGACCCCTCCG | 284434 |
rs556769083 | in-del | -/AT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16725008 | CAAAAATTTTTATTT[-/AT]TTTTTATTTTTTTAT | 284434 |
rs556782193 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16719427 | CAGGCATGAGCCACC[A/G]TGCCCGGTCTTGGAG | 284434 |
rs556810160 | in-del | -/GAG | 1.64874e-05 | 0.00287113 | cds-indel | NWD1 | GRCh38.p7 | 19:16788984 | TGGCCTGCTGCAGGA[-/GAG]GTGAGGTGTGTGAAA | 284434 |
rs556816698 | snp | A/C/T | 6.8421e-05 | 0.00584863 | missense | NWD1 | GRCh38.p7 | 19:16759335 | AGCTGCTGCGCTTCC[A/C/T]GCCCCTGCTGTGGGT | 284434 |
rs556824082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16788187 | ATAAGCCAGGGCCAC[A/G]CCACTGCACTCCAGC | 284434 |
rs556876535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748564 | GGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 284434 |
rs556918817 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16778982 | TCCCTGGCCTGCACC[A/C]ACCAGATGGCAGTAC | 284434 |
rs556928013 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16754146 | GACCTTTCATCCATC[C/T]GTCCATCATCTCTAT | 284434 |
rs556965378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16791915 | GACAGGGTTTCTCCA[C/T]GTTGGTCAGGCTGGT | 284434 |
rs556978414 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16785239 | GTGATAGGCCAGGCG[C/T]GGTGGCTCACGCATG | 284434 |
rs556982405 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16719733 | AGACTGTCAGCAAAT[A/G]GCATCTTTTACGAGG | 284434 |
rs557002108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16803683 | GAACTTTGGGAGGCT[A/G]AGGTGGGCGGATCAT | 284434 |
rs557029258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16735128 | CGCATGGACAGTACG[A/G]AGTTCCCATACACCC | 284434 |
rs557085290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16797281 | GAATCCACCTTCCCC[A/G]TCCTGGATCCCTTCT | 284434 |
rs557095264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16724841 | GGGACTACAGGCATG[C/T]GACACCATACCCAGC | 284434 |
rs557098665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16779590 | CCTGCATCACTTAGC[C/T]ATAGTTGCATAATGA | 284434 |
rs557116936 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16783945 | GGCCGGGCACAGTGG[A/T]TCACGTCTGTAATCC | 284434 |
rs557160360 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16785869 | GACTCTTTTTTTTAA[A/T]TTTTTTTGTTTTTGA | 284434 |
rs557162779 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16730305 | CCAGCCTGGTGACAG[A/C]GTAAGACTTCGTCTC | 284434 |
rs557195351 | in-del | -/AAC | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16730345 | CTAACAAAAAAACAA[-/AAC]AAAAAAAACCCAAAA | 284434 |
rs557219879 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16729796 | ATCCCTTGAATCTGG[G/T]AGGCGGAGGTTGCAG | 284434 |
rs557280248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16809321 | GGCCTCAAGTGACCT[A/G]CCTTGGCCTCCCAAA | 284434 |
rs557297081 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16733733 | TGGTCAAGCTTTTCT[C/G]TTTAATGCCCATGCC | 284434 |
rs557313447 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16730193 | CAGGTGTGGTGGTGC[A/G]CGCCTGTAATCCCAG | 284434 |
rs557367622 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16792308 | CACTTTGGGAGGCTG[A/T]GGGGGGGTGGATCAT | 284434 |
rs557421377 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16740064 | CGCTTTGAGAGGCTA[A/C]AGCCGGAGGATCGTG | 284434 |
rs557437100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16787251 | CCCACCTCAGCTTCC[C/T]GAGTAGCTAGGACCA | 284434 |
rs557501486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16809836 | TGCTGGGATTACAGT[C/T]ATGAGCCACCGTGCC | 284434 |
rs557504105 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16807256 | CCCAGCACTTTGGGA[G/T]GCCAAGGTGGGTGGA | 284434 |
rs557530635 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16752436 | TGAGGTGGGAGGATC[A/G]CTTGAATCCAGGAGT | 284434 |
rs557561275 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16727779 | AGAGACCTAGACGTG[A/G]ACCAAGTACTGTGTT | 284434 |
rs557612551 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16770730 | ACAGAACCTCCACCC[A/G]TGTTGCCATCGAGGG | 284434 |
rs557622605 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | NWD1 | GRCh38.p7 | 19:16727547 | GGTCATCTTGGTGGG[C/T]GGGCGGCAATGAGCG | 284434 |
rs557626904 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16812932 | CCTGGGCATTAGAGG[G/T]CCCTGCTCTGGCCAC | 284434 |
rs557646770 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NWD1 | GRCh38.p7 | 19:16771189 | GGGCACAGTGGCTCA[C/T]GCCTGTAACCCCAAT | 284434 |
rs557667518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16812352 | GGCTGGTTTCCTGGG[C/T]GTCTTTCAGTTTGGA | 284434 |
rs557709824 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16770596 | GGCAGTGTGACCTTG[A/C]AAACCCTTTACCATC | 284434 |
rs557711587 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16774078 | CATCCATCCATCCAC[C/T]GTCCTCCCACCCACC | 284434 |
rs557720513 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16766809 | CAGGCAGGTCTTGAA[C/T]TCCTGGACTCAAGCA | 284434 |
rs557782123 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16766103 | AAATTATGTAGGTAC[A/G]TATATGATAAGAGAG | 284434 |
rs557811607 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16796683 | ATTTCTCTCCTTCCT[C/T]CCTTCCTCTTTACTT | 284434 |
rs557843810 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16727183 | GGTCCCCGGGCCCCA[A/G]TGCCCAGCACTGGGA | 284434 |
rs557845377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16772732 | CCCTAGTATTTGGGA[A/G]GCTGAGATGGGAGGA | 284434 |
rs557861385 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16745294 | TCCCTCCCACAGCAC[A/G]TGTGAATTATGGGAG | 284434 |
rs557886664 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800252 | CAAATCATCCCCACA[G/T]GCTGGGCCCCATGGC | 284434 |
rs557893153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16731804 | TTTACTGTTGAGTTT[C/T]AAAATTCACAGTGAT | 284434 |
rs557898346 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16794101 | CTAGGCATGGTGGCT[C/G]ACGCCTGTAATCCCA | 284434 |
rs557942479 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16807145 | GTGAGCTTCAGTCTC[A/G]CCACTGCACTCCAGA | 284434 |
rs558000463 | snp | A/G | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817232 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC | 284434 |
rs558014578 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16798588 | TGCACTTCAGCCTGG[A/G]TGACAAAACAAGAAC | 284434 |
rs558050418 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16803927 | AGACTCCACCACCCG[-/A]AAAAAAAAAAGAAAA | 284434 |
rs558090248 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16813216 | GGAGCTGAGAAGAGT[G/T]AGAAGAGGGTCAAGT | 284434 |
rs558097650 | snp | A/G | 0.139225 | 0.224118 | intron-variant | NWD1 | GRCh38.p7 | 19:16799664 | GGCATGCACCACCAA[A/G]CCTGGCTAATTTTTT | 284434 |
rs558104379 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16805502 | CCTGGTTAATTTTTT[A/T]AATGTTTTTGCAGAG | 284434 |
rs558194700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16811352 | ACTTTGGGAGGCTGA[A/G]GCGGGTGGATCACTT | 284434 |
rs558215117 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16726297 | ACTTTTTTTTGCAGA[C/G]ATGAGGGCTCACTGT | 284434 |
rs558242698 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16802292 | ATAAATAAATAAATA[A/T]AAATAAAAATAAAAA | 284434 |
rs558244333 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16769827 | CTGTTTTCCATCTGT[A/C]TTGGCTCTTTTTCTT | 284434 |
rs558280875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16810495 | AGTCTAGATTAGGCA[C/T]AGCAACTCATGCCTG | 284434 |
rs558282628 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16818077 | GAAAGGCCAAGGTAG[A/G]AGGATCACTTGAGCC | 284434 |
rs558295751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16791251 | AAAGAAAAGAAAATG[C/T]ATAAAGTATACAAGA | 284434 |
rs558319674 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817550 | GAGGTTGCAGTGAGC[C/T]GAGATCGCACCACTG | 284434 |
rs558339368 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16766386 | CAGCCTGGGTGACAG[A/C/G]GCGAGACCCTGTCTC | 284434 |
rs558359681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16728838 | AGCCCCAGCTGCTCG[A/G]GAGGCTGAGGCAAGA | 284434 |
rs558405345 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16755468 | ATCTCAGCTCACTGC[A/C]ACCTCCGCCTCCTAG | 284434 |
rs558419520 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16799015 | CACCCTCTAAAAAAG[A/G]TTTACAGGGCACCCT | 284434 |
rs558438466 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16780665 | CCTTTTCTTTTTCTC[A/G]TTCTTTTTTTCTGAC | 284434 |
rs558471915 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16745806 | CCTGTAGCCCCAGCT[A/G]CTCAGGAGGCTGAGA | 284434 |
rs558472896 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16743973 | CAGGTGTGAGCCACC[A/G]CGCCTGGCCGATATA | 284434 |
rs558505148 | in-del | -/C | 0.0154538 | 0.0865337 | intron-variant | NWD1 | GRCh38.p7 | 19:16730914 | TTTCTTTCTTTCTTT[-/C]TTTTTTTTTTTTTTG | 284434 |
rs558562223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16796519 | GATTTCATTTGGAAA[C/T]AGCAGCCCAGGCTGT | 284434 |
rs558574850 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16770421 | TTCCTGAGGCCTCCC[A/C]AGCCCTGCAGAACTG | 284434 |
rs558604512 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16778803 | TATTGGCCTCCCACA[A/G]TGCTGGGTGGCATGA | 284434 |
rs558608259 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16752247 | TCAGCCTGTGCCATT[G/T]CAGACCTTTGTCGGT | 284434 |
rs558669705 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16737665 | CCAAGAACGATCACA[-/T]TTTTCCTTAGAAATT | 284434 |
rs558683385 | snp | C/G | 1.64741e-05 | 0.00286998 | utr-variant-3-prime, missense | NWD1 | GRCh38.p7 | 19:16815162 | TCAGCAAAAGCCTCA[C/G]CGCAGGACCCTCTTA | 284434 |
rs558685317 | snp | A/G | 6.59011e-05 | 0.00573988 | missense | NWD1 | GRCh38.p7 | 19:16807976 | TCTTTCTTTACGAGT[A/G]TGCAACTTCCAAAGC | 284434 |
rs558692552 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16750916 | CCTAGTAAAAGTCTC[A/G]GAGCTATAAATTGCA | 284434 |
rs558696655 | in-del | -/AAAC | 0.00438769 | 0.0466326 | intron-variant | NWD1 | GRCh38.p7 | 19:16812675 | CTCCATCTCAAAAAC[-/AAAC]AAACAAACAAACAAA | 284434 |
rs558705401 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | NWD1 | GRCh38.p7 | 19:16766305 | TACTTGGGAAGGTGA[G/T]GTGGGAGGATCAATT | 284434 |
rs558745527 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16757192 | GAAAAAAATTGTCTT[A/C]CAAGAAACCGGTCCC | 284434 |
rs558832639 | in-del | -/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16728281 | TGCTGGGTCACTGCT[-/C]TTTTTTTTTTTTTTT | 284434 |
rs558840173 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16788135 | CTCGAGAGGCTGAAA[C/G]AGGAGAATTGCTTGA | 284434 |
rs558858916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16776161 | CATTTTTCTCATCTC[C/T]GGGGCAGGGAAATGT | 284434 |
rs558870639 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16746285 | GGATTGCGTCAGCCT[A/G]GGAGGCGGAGATTGC | 284434 |
rs558896238 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718704 | TTTTTTGTTTTTTGT[C/T]TTTTATGTAGAGACA | 284434 |
rs558897779 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16733773 | ACGCGGATGCTGTCA[A/G]CATCCTCCACACGCA | 284434 |
rs558956115 | snp | A/G | 0.000495074 | 0.0157255 | intron-variant | NWD1 | GRCh38.p7 | 19:16788946 | GGCCAAAATGTTCCC[A/G]GCTAATATACTCTCC | 284434 |
rs559019073 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16795096 | GCCCTTTCTTTCCTT[A/T]TGATGCAGGATTTTT | 284434 |
rs559026309 | in-del | -/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16766032 | AAAAAAAAAAAAAAA[-/G]AAAGAAAGAAAGAAA | 284434 |
rs559077833 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732031 | AGACTAGCCTAGGCA[A/G]CATGATGAAACTCTG | 284434 |
rs559083235 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16794687 | CAAATGGCCTCATAG[G/T]AAACATTTTTTGCAG | 284434 |
rs559103963 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816324 | TTCTGACTTTTAAAG[C/T]TGGCGATTGGTTGAA | 284434 |
rs559120178 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16762976 | TTTAGTAGAGACGGG[G/T]TTTTGCCATGTTGGC | 284434 |
rs559128852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16733963 | ATGTGTCTTTCTCTC[A/G]GTGCTAAAGAATTCA | 284434 |
rs559131794 | snp | C/T | 0.133777 | 0.221342 | intron-variant | NWD1 | GRCh38.p7 | 19:16778491 | TTTCTTCTTCTTCTT[C/T]TTCTTTTTTTTTTTT | 284434 |
rs559187904 | snp | A/G | | | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16717858 | TCTTTTTCTTTTTTT[A/G]TTTTAAAGAGACAGG | 284434 |
rs559203222 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16782420 | GCAGTGAGCCATGTT[C/T]GCACCACTGTATTCC | 284434 |
rs559237464 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16782951 | TCCCTTCCTTCCCCC[A/C]TTCCCCTTCCTCCCT | 284434 |
rs559240240 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16726505 | AGTGCAGTGGTGTGA[A/T]CTTAGTTCACTGCAA | 284434 |
rs559257338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16814121 | GCCATGATAGCACCA[C/T]TGCACTCCAGCCTGG | 284434 |
rs559262641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16766215 | GGTTTTCACTATTAT[C/T]TGGTCCATTGCAAAC | 284434 |
rs559263750 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16755279 | GGAGTGCACTGAAGC[A/G]ATCACAGCTCGCCGC | 284434 |
rs559298104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16789619 | TCTGGATAGGGTCCT[A/G]TTCTGTATTTTTTTT | 284434 |
rs559304335 | snp | A/G | | | intron-variant, synonymous-codon | NWD1 | GRCh38.p7 | 19:16812846 | TGTTTGGAGTGTGCT[A/G]GATGGTGAGTCATTT | 284434 |
rs559340194 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16723857 | TGCACCGTCATGCCC[A/G]GCTAATTTTTGTATT | 284434 |
rs559432416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748175 | TTTTAGTAGTGACAA[A/G]GTTTCACCATGTTGG | 284434 |
rs559433361 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16730685 | TTGCACCACTGCCCT[C/G]CAGCCTGGGTGATGG | 284434 |
rs559433564 | in-del | -/TCCA | 0.175587 | 0.238669 | intron-variant | NWD1 | GRCh38.p7 | 19:16754466 | CATCTCTATTTTCCA[-/TCCA]TCCATCCATCCATCC | 284434 |
rs559447219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16814896 | AGGGACTCTTTGGCA[C/T]AATAAATGTCATGCC | 284434 |
rs559499680 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16784756 | CAACATGGTGAACCC[C/T]TGTCTCTACTAAAAA | 284434 |
rs559554276 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16805027 | AATATTTATTTATTT[A/T]TTTATTTTTATTTTT | 284434 |
rs559575463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16729393 | GGACTATCACTCTCA[C/T]GGTTCCCTCTTCTCC | 284434 |
rs559590488 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16810651 | GCCTGTAGTCCCAGC[C/T]AGTTAGGAGGCTGAG | 284434 |
rs559590630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16804319 | GGTGTGGTGGCTCAT[A/G]CCTGTAATCCCAGCA | 284434 |
rs559594039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16803336 | AACACCAACAGACTT[A/G]GACAGGCCCCAGCTC | 284434 |
rs559594262 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16736857 | ACCGTTTCTGCTTTC[A/G]TACCTTATCCCTATG | 284434 |
rs559615668 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718894 | CAGTGGTGCGATCTC[A/G]GCTCACTGCAAGCTC | 284434 |
rs559628939 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817127 | ACAACATGGTGAAAC[C/T]CTTCTCTACTAAAAA | 284434 |
rs559635485 | in-del | -/GCTCACT | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16732704 | TGGTGTGATCTCACA[-/GCTCACT]GCTCACTGCAACCTT | 284434 |
rs559641372 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16734626 | CTGTCACCCAGGCTG[G/T]AGTGCAGGCATGCAA | 284434 |
rs559651517 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16781545 | CGCTTGAGCTCAGGA[G/T]ATTGGGGCTACAGTG | 284434 |
rs559716783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16729974 | CCTGTTATTCTCTAG[C/T]CCAGCCCACCCGTGT | 284434 |
rs559740072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16770695 | TAGGGCTGCTGGGAA[A/G]AGTACGCGCATCAGT | 284434 |
rs559741593 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16721424 | GGGAGCGTGGCCAGG[C/T]GCTGAAGTGAATTCG | 284434 |
rs559783842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16735206 | TATGTTGTTACAACT[A/G]TGAAATGAACTTTGA | 284434 |
rs559793729 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16796809 | TTTCTGAGATACCAT[G/T]ATGAGCCAAATAGGC | 284434 |
rs559806759 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16805911 | TTTCCATCTGTTGCC[C/T]GGGCTGGAGTGCAGT | 284434 |
rs559832161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16806421 | TACAAAAGTCTGGCC[C/T]CCTTGCTTCAAGATG | 284434 |
rs559856464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16722014 | GCTACTTGAGACGCC[A/G]AGGCAGGAGGATGGT | 284434 |
rs559877928 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16746457 | AGGCAGACGGATCAC[A/G]AGGTCAGGAGTTCAA | 284434 |
rs559920401 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16779741 | CTCCTGGGCCAAGTG[A/T]TCCTCCTGCCTCAGC | 284434 |
rs559952031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16767885 | ATTTCATATAAGTGG[C/T]ATTTTACAGTATTTG | 284434 |
rs559991836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16728813 | GCTAGGCGTGGTGGC[A/G]GGCGCCTGTAGCCCC | 284434 |
rs560011150 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16774191 | CTCTCCCATCCATCT[A/G]TCCTCCCACCCTTCC | 284434 |
rs560012383 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800344 | TTCAAGACCAGCCTG[A/G]CCAACATGGCAAAAC | 284434 |
rs560040873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16759589 | TTATTTTTAAAATTG[A/G]GTTGAGGCTGGAAGC | 284434 |
rs560063122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16788397 | AACATAGTCAAACCC[A/G]TCTCCACTAAAAATA | 284434 |
rs560096144 | snp | A/G | 5.11261e-05 | 0.00505573 | missense | NWD1 | GRCh38.p7 | 19:16750317 | CCGCTGGCCACCACC[A/G]CAGAGGAAGCCACGC | 284434 |
rs560214388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16767328 | GCCTTATAAAACCAT[C/T]GGACGGCCAGGTGTG | 284434 |
rs560222360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16811597 | CTCAGAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 284434 |
rs560231020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16760932 | TATTTTAGTACACTC[A/G]TAATGTTGCACCCCT | 284434 |
rs560248721 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764939 | CTGCTGAGCCTGAGA[A/T]GCCCTGGAGGAAATG | 284434 |
rs560260621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16793333 | CGACCTCCCGGGCTC[A/G]AGACGTCCTCTCGCC | 284434 |
rs560282521 | in-del | -/TTTATT | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16805028 | ATATTTATTTATTTA[-/TTTATT]TTTATTTTTATTTTA | 284434 |
rs560321172 | in-del | -/A | 0.160938 | 0.233598 | downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16818118 | AGACCCTGTCTCTCC[-/A]AAAAAAAAAAAAAAA | 284434 |
rs560327017 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16787723 | AAATTAGCCAGGCGC[A/G]GTGGCACATGCCTGT | 284434 |
rs560363206 | snp | C/G/T | 3.33224e-05 | 0.0040817 | missense | NWD1 | GRCh38.p7 | 19:16750083 | TTGGACACCTTGCAG[C/G/T]GGGTGCTCCTGGACC | 284434 |
rs560363599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16780256 | TGCCTCCCAGGTTCA[C/T]GCCATTCTCCTGCCT | 284434 |
rs560376042 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16742472 | ATCTCTCCCTTTCTC[C/T]GTGGTCAGCCCTTAA | 284434 |
rs560391687 | snp | A/C/G | 0.000160377 | 0.00895351 | splice-acceptor-variant, intron-variant | NWD1 | GRCh38.p7 | 19:16794461 | TCCCTGGTTCTGCAC[A/C/G]GGTTTCCTCCAAAGG | 284434 |
rs560401340 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16754525 | TCTCTATCTTCCATT[C/T]ATCTATCCATCATCT | 284434 |
rs560426703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16786658 | TTCAAGCGAGTTTCC[C/T]GCCTCAGCTTCCCGA | 284434 |
rs560434654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748549 | TGGCTAAATCAGGCC[A/G]GGCGCAGTGGCTCAC | 284434 |
rs560546934 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16721329 | AGGAAGTCTGGGAGA[A/G]AGACTAGGAAAAAGC | 284434 |
rs560570514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16792648 | GATTGCACCACTGCA[C/T]TCCAGCCTGGACATT | 284434 |
rs560606741 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16742796 | TTGCCTCAGGCTCCC[A/G]AGCAGCTGGGACTAC | 284434 |
rs560633967 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16723555 | CTGGGCTCAAGCAAT[C/T]CCCACCTCAGCCTCT | 284434 |
rs560645702 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16773770 | TCATTTTTTTCTTCC[G/T]TCCATTCATCCAACC | 284434 |
rs560672593 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16779244 | TCTCTGTGCCTCAGT[A/T]GTCTTATCTGTGAAG | 284434 |
rs560679366 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NWD1 | GRCh38.p7 | 19:16751181 | GTGAGCCGAGATCAC[A/G]CCATTGCACTCCAGC | 284434 |
rs560681575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16758181 | CAGAAACTGAATTTA[A/G]AACTTTGAAAGATGG | 284434 |
rs560684032 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16766549 | CCATGAGGATGTTCT[A/G]TTTGGTTTTGTTTTA | 284434 |
rs560725283 | in-del | -/GA | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16777180 | AAGGGGAGGGAAGGG[-/GA]AAGGGGAGGGGAAAG | 284434 |
rs560739536 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16737976 | TCTCGAAAAGAAAAG[A/C]AAAGAAAAGAAAAGA | 284434 |
rs560793198 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16776880 | CCAAGAGTTCGAGGC[C/T]GCAGTGAGCTGTGAT | 284434 |
rs560892756 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16814295 | AAGGTCACACAGTGA[A/G]TAACTAGTAGGCTTA | 284434 |
rs560901780 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16754182 | ATCCATCTATCCATC[A/G]TCTCGATCTTCCATC | 284434 |
rs560910379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16790526 | GCATGTGGGGCTTAA[A/G]ACCTAGATGACGGGT | 284434 |
rs560913403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16770755 | CGAGGGTCCTGTTAC[C/T]GTCATATGATAGCAT | 284434 |
rs560953210 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16776202 | AGATCCACTGTGCCC[C/T]GCTGTACATCCTCTA | 284434 |
rs560955688 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16741375 | GTTTTTGTGTTTTTT[G/T]TTTTTTTTTTGAGAC | 284434 |
rs560962820 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718360 | TTGTTTTTAGTAGAG[A/T]TGGGGTCTCACCATA | 284434 |
rs560971143 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16818311 | GAAAAAAAATAAAAT[A/T]AAATTAAGGGATGCC | 284434 |
rs561017699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16740761 | ACAGGTGTGAGCCAC[C/T]GCACTGGCCCAGGTT | 284434 |
rs561068819 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16742272 | CCCAGCTACTCAGGA[A/G]GCTGAGGCCGGAGAA | 284434 |
rs561119774 | in-del | -/AAA | 0.485664 | 0.0834419 | intron-variant | NWD1 | GRCh38.p7 | 19:16732217 | GTGAGACTCCGTCTC[-/AAA]AAAAAAAAAAAAAAA | 284434 |
rs561141484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16757601 | CAGCCCTGTTTTGCA[A/G]TTCAGGCTAGGCGGG | 284434 |
rs561146349 | snp | A/G | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16734788 | ACAATGTCTCCCTAT[A/G]TTGTTCAGGCTGGTC | 284434 |
rs561174445 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16796335 | GGCATGGTGGCAGGC[A/G]CCTGTAATCCCAGCT | 284434 |
rs561214945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16742773 | CCTCCAGGGTTCAAG[C/T]GATTCTCTTGCCTCA | 284434 |
rs561272526 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16802865 | ACTTAGCCAGAAATC[A/G]CTTGAACCCAGGAGG | 284434 |
rs561280168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16747512 | CTTCCCAGTAGCTGG[A/G]ACCGCAGTCACACGC | 284434 |
rs561308549 | snp | C/T | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748180 | GTAGTGACAAGGTTT[C/T]ACCATGTTGGCCAGG | 284434 |
rs561309528 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16774855 | CATTCATTCACTTAC[A/G]CCTCCACCCATCCAC | 284434 |
rs561315698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16782496 | ACAGAAAAATGGGTG[A/G]GGGTGGAGAAGGTCT | 284434 |
rs561345788 | in-del | -/TT/TTTTT | 0.0646061 | 0.168308 | intron-variant | NWD1 | GRCh38.p7 | 19:16804594 | GACCCTGTCTCTCTG[-/TT/TTTTT]TTTTTTTTTTTAATT | 284434 |
rs561352648 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16813223 | AGAAGAGTGAGAAGA[G/T]GGTCAAGTCACTAGT | 284434 |
rs561379147 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16781713 | ACATACTCCATGCTT[A/C]TTTGTTGAATAAATA | 284434 |
rs561409413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16728670 | TAATTGCAGGCCGGG[C/T]GCAGTGGCTCACACC | 284434 |
rs561427120 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16737263 | AATGATATTCCTGAG[G/T]CTTTTTTCTTTTTCT | 284434 |
rs561439620 | snp | C/T | | | synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744681 | CCGGAGGCTGGGGCT[C/T]ATCACCCAGGAGCAG | 284434 |
rs561452049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16813917 | AGCACTTTGGGAGGC[C/T]GATGTAGGAGGACTG | 284434 |
rs561471557 | snp | C/T | 1.64768e-05 | 0.00287021 | missense | NWD1 | GRCh38.p7 | 19:16808021 | CCCACAGGAGCCGAG[C/T]TGCCTGTGTGGAGGT | 284434 |
rs561485899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16801351 | GGCTAAGGTGGGAGG[A/G]TCGCTTGAGCCTGGG | 284434 |
rs561492885 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16723644 | TTATATCCATTCATC[A/T]TAACCTATGAGTACC | 284434 |
rs561551403 | in-del | -/TTA | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16781658 | TGTTGACCTGAGATC[-/TTA]TTACTATTGTTTGAG | 284434 |
rs561551744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16810102 | AGGAGAACTCCTGAC[A/G]TTTCCTTGATGCTCA | 284434 |
rs561586237 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817328 | TAATGGCAAAAGCCT[C/T]GGTGGCTCACGCCTG | 284434 |
rs561654797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16773065 | GGAGCAGAGACTCAA[C/T]TGGCAGGGAGGGTAG | 284434 |
rs561676002 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16790600 | ACAAACCTGCACGTT[C/T]GGCACATGTATCCCA | 284434 |
rs561688527 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16792811 | GAACCCGGGAGGTGG[A/C]GGTTGCAGTGAGCCG | 284434 |
rs561696818 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16721210 | GTGTGCTGTTGAAAT[C/G]TAGTGGGTGGGGGCC | 284434 |
rs561711089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16779765 | CCTCAGCCTCCTGAG[C/T]AGCTGGGACTACAAG | 284434 |
rs561731904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16761565 | ACAGGGTTTCACCAC[A/G]TTGGCCAGGCTGGTC | 284434 |
rs561740152 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16805723 | TTGCTCCCTGCCAAC[C/T]CCCAGAGCTTTGCCT | 284434 |
rs561821036 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NWD1 | GRCh38.p7 | 19:16799415 | TGGCCAGGATGGTCT[C/T]GATCTCCTGACCTCA | 284434 |
rs561862043 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16743975 | GGTGTGAGCCACCGC[A/G]CCTGGCCGATATACA | 284434 |
rs561881759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16798546 | AGCCTGGGAGGTAGA[A/G]GCTGCAGTGAGCTGT | 284434 |
rs561947173 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16720842 | ACAGGCGTGAGCCAC[C/G]GCACCTGGCCGAGAC | 284434 |
rs561966485 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718945 | TTCTCCTGCCTCAGC[C/T]TCCTGAGTAGCTGGG | 284434 |
rs561977423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16761026 | TCACTCCTCATTCCC[C/T]TTCCCTAACCCCTGG | 284434 |
rs561993679 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16737995 | GAAAAGAAAAGAAAA[C/G]AAAAGAAAAGAAAAG | 284434 |
rs562030598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16724489 | GTTCTCTCTGCCTCC[A/G]GCGGTGGTTTGCTAC | 284434 |
rs562040187 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16766337 | AGCCTGGGAGGTCGA[C/G]GCTGCAGTAAACTGT | 284434 |
rs562053034 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16808417 | TAGCCAGGTGTGGTG[G/T]TGCATGCTTGTAATC | 284434 |
rs562059227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16759645 | ACTTTGTGGGGCCAG[A/G]GCAGGAGGATTGCTG | 284434 |
rs562073380 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16809031 | ACTGCTCTCTAGCCT[A/G]GGTGATAGAGCAAGG | 284434 |
rs562098613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16801139 | ACAAAATTAGCTGGG[C/T]GTGGTGGTGCATGCC | 284434 |
rs562147137 | snp | A/G | 0.127254 | 0.217792 | intron-variant | NWD1 | GRCh38.p7 | 19:16743672 | TTTATTTATTTATTT[A/G]TTAGTTTGTTTATTT | 284434 |
rs562148454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16730463 | TCACTCCTGTAATCC[C/T]AGTGCTTTGAGAGGC | 284434 |
rs562160488 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800462 | TTTGAACCTGGGAGG[C/T]GAAGACTGCAGTGAG | 284434 |
rs562204711 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NWD1 | GRCh38.p7 | 19:16809541 | GTGCTATTTCTTTTT[C/T]TTTTTCTTTTTCTTT | 284434 |
rs562242672 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816125 | AATCTAGACACTTCC[A/T]TGCACCTGGGTGAGC | 284434 |
rs562281143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16785507 | CAGAGTGAGACTCTG[C/T]CTCAAAAAAATAAAA | 284434 |
rs562311745 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748756 | TTGAGCCTAGGAGGC[A/G]GAGGTTGCAGTGAGC | 284434 |
rs562338315 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16792071 | AGTTCAGGAAACATC[A/T]GTTGGCGTCTCTTGG | 284434 |
rs562339697 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16754245 | ATCCATCCATCATCT[A/C]CATCTTCCATCCATC | 284434 |
rs562342829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16756970 | TATGAGAATCTAATG[C/T]CTGATGACCTGTCAC | 284434 |
rs562393268 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16741865 | CCTGTAATCCCAGAA[C/T]GTTGGGAGGCTGAGG | 284434 |
rs562401925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16753534 | TCTAGGCTAGAGGTC[A/G]TCACCTCAGGATAGT | 284434 |
rs562405165 | in-del | -/TAATAA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16788280 | TAATAATAATAATAA[-/TAATAA]AAGGCCAGGCATGGT | 284434 |
rs562405976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16762766 | TTTGGTGCTGCCTTT[C/T]CTTTTTCCCTCCCTC | 284434 |
rs562435711 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16795245 | GCCCCTAGCAGGAGG[C/G]AGCATGTGAGCAAGT | 284434 |
rs562546617 | snp | A/G | 5.0452e-05 | 0.00502229 | missense | NWD1 | GRCh38.p7 | 19:16749979 | ACCTGGACTCTGTCC[A/G]CCATGCTCGGAGGGT | 284434 |
rs562558697 | in-del | -/T | 0.0912534 | 0.193131 | intron-variant | NWD1 | GRCh38.p7 | 19:16771832 | CGCGATCACGAGTCC[-/T]TTTTTTTTTTTTTTT | 284434 |
rs562569748 | snp | A/G | 6.58913e-05 | 0.00573945 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16789049 | TTCAAAGGATTACAC[A/G]CTGCACTTGTGGAAC | 284434 |
rs562592477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16722098 | AATCTGGGCAATGGA[A/G]TGAGACCCTGTCTCT | 284434 |
rs562600394 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16771981 | TTTTCTTAATAGCCC[A/G]TTTTTTAATAGAACG | 284434 |
rs562623831 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732600 | TCCCTGGCTAGGGAA[C/T]TTTTTTTTTTTTTTC | 284434 |
rs562626820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16762266 | TTTCCGCACAGAGGG[C/T]AAGATGTCCCTTCTA | 284434 |
rs562675322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16746423 | CTCATGCCTGTAATC[C/T]CAGCACTTTGGAAGG | 284434 |
rs562689568 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16774276 | CATTCATCCAATCAT[C/T]TACCCACCCTTCCAT | 284434 |
rs562727572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16774649 | ATCCTTTCATCCGTC[C/T]ATCCACCCACCCTTC | 284434 |
rs562727576 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16768045 | CACCCAGGCTGGAGT[G/T]CAGTGGCACGATCTC | 284434 |
rs562734799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16746116 | TCCCAGCACTTTGGG[A/G]GTCTGAGGTGGGTGG | 284434 |
rs562736655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16750999 | GGCCGAGGCGGGCGG[A/G]TCACCCAAGGTTGGG | 284434 |
rs562755799 | in-del | -/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16766883 | AACCACTGTGCCTGA[-/C]CCCCCATCTTAACCA | 284434 |
rs562772587 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751255 | AATGCAATAAACTTG[G/T]GTCATGATAGTCTGG | 284434 |
rs562795341 | snp | C/T | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16788437 | AGCCAGGCATGGCGG[C/T]AGGTGCCTGTAATCC | 284434 |
rs562796972 | snp | A/G/T | 3.81914e-05 | 0.00436973 | missense | NWD1 | GRCh38.p7 | 19:16750411 | ACATTGTGTCTTCCC[A/G/T]GTAAGTCTCTGTGTT | 284434 |
rs562845977 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16773684 | AGAAGCTGAAGGAAC[C/T]GTAAGCAGCCCTTGG | 284434 |
rs562866996 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16780312 | AGGCGCCCGCCACCA[C/T]GCCTGGCTAATTTTT | 284434 |
rs562902313 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16794276 | GAGGCTGAGGCAGGG[A/G]AATTGCTTGAACCCG | 284434 |
rs562903674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16745048 | TAATTTACAAAGGAA[A/G]GAGGTTTAATGGACT | 284434 |
rs562930197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16786717 | ACACCCAGCTAACTT[C/T]CGTATTTTTAGTAGA | 284434 |
rs562944881 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16738518 | AGGTTGGAGTGAGCC[A/G]AGATTGTGCCACTGC | 284434 |
rs562945765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748133 | GGATTACAGGCGTGC[A/G]GCATCACGCTGGGCT | 284434 |
rs562963384 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16793558 | TTTTTTTTTTAACTG[G/T]TTTTTTGTTTTTTGG | 284434 |
rs563007163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16747633 | CAGCCTCTGCCTCCC[A/G]AAGTGCTGAGATTAC | 284434 |
rs563048889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16780830 | ACCTGGCTGATTTTT[A/G]TATTTTTTGGTAGAG | 284434 |
rs563049264 | snp | C/T | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816814 | TTATTCATCCATTTT[C/T]CAAACCAGTTTTCCA | 284434 |
rs563080475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16745388 | GGCGACTACCATCCC[A/G]GTTTGCCTGGGACGG | 284434 |
rs563081333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16752738 | GTGGTGGCTCACACC[C/T]GTAATCCCAGCACTT | 284434 |
rs563093027 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16732944 | TTAAAAGATGAGGCC[A/G]GGCACAGTGGCTAAC | 284434 |
rs563106520 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16777111 | AGGGGAAAGGGGAAG[A/C]AAGGGAAGGGGAGGG | 284434 |
rs563119578 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16772095 | TTGAGTCTGAGCACA[C/G]TGGCTCACGCCTATA | 284434 |
rs563180954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16771394 | GGCAGATGTTGCGGT[A/G]AGCCGAGATCACGCC | 284434 |
rs563263471 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16784704 | GGGAGGCCAAGGTGG[G/T]CAGATCACGAGGTCA | 284434 |
rs563283081 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16736290 | GCTGGCATGCAGTAG[G/T]ACAATAAGAGCTCAC | 284434 |
rs563299138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16729223 | GTGTCAGGCTTAAAA[A/G]CTGCCAGAACCTTGC | 284434 |
rs563300977 | snp | A/T | 1.66247e-05 | 0.00288307 | intron-variant | NWD1 | GRCh38.p7 | 19:16791340 | TGCTTCCTCTTCATT[A/T]TTCTATTAGATCAAT | 284434 |
rs563328787 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16813988 | AGACTCTGTCTCTAC[-/A]AAAAAAAAAAAAATT | 284434 |
rs563360422 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16728719 | GGAGGCCGAGGCGGG[A/C]GAATCACGAGGTCAG | 284434 |
rs563364204 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16790719 | TGAAATTCAAAGACC[A/T]AGTATAGTAAAAATA | 284434 |
rs563427915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16725128 | ACGCAATTCCCATGC[C/T]TCAGCCTCTCGAATA | 284434 |
rs563474751 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16735399 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 284434 |
rs563498167 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817043 | CAGTGGCTCACACCT[A/G]TGGTCCCAGCTCTTT | 284434 |
rs563513700 | in-del | -/ATTATT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16742919 | ATTATTATTATTATT[-/ATTATT]TTATTTGAGACAGAG | 284434 |
rs563539984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16752227 | AGGGTTGTTTTTTTT[C/T]TTTCTCAGCCTGTGC | 284434 |
rs563632397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16723755 | CCAAGGCTGGGTGTG[A/G]TGTGATCTCAGCTCA | 284434 |
rs563670521 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16779591 | CTGCATCACTTAGCT[A/G]TAGTTGCATAATGAA | 284434 |
rs563713250 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16775722 | CGCCCAGGCTGGAGT[G/T]CAGTGGCGCAATCTC | 284434 |
rs563714206 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16734562 | AAGATTTTCTTTCTT[A/T]TTTTTTTTCTTTTTT | 284434 |
rs563723068 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16805876 | TTCTTTCTTTTCTTC[-/T]TTTTTTTTTTGAGAG | 284434 |
rs563733413 | in-del | -/CATC | 0.00955202 | 0.0684454 | intron-variant | NWD1 | GRCh38.p7 | 19:16754707 | ATCATCTCTAGCATC[-/CATC]CATCCATCCATCCAT | 284434 |
rs563760678 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16726642 | ACAGGGTTTCACCAT[A/G]TTGGCCAGGCTGGTT | 284434 |
rs563762873 | snp | A/C/G | 0.00199529 | 0.0315338 | intron-variant | NWD1 | GRCh38.p7 | 19:16811499 | TGAGGCAAGAGAATC[A/C/G]CTTGAACCCAGGAGA | 284434 |
rs563780091 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16758257 | CCAGTTTAACTTTAT[G/T]TGTATTTATTTGTTC | 284434 |
rs563799057 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16818285 | GGGCAAGAGAGTGAG[A/T]CCATGTCTCAGAAAA | 284434 |
rs563824268 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16801916 | ACCCCAGCTACTCAG[C/G]AGGCAGAAACAGGAA | 284434 |
rs563840540 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16763759 | AGCATGAGGTGAATG[A/G]ATGGGCTTGTGCGTG | 284434 |
rs563888203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16796131 | GTAGTATTGGAAAAC[A/G]TAACATTCAATTGGT | 284434 |
rs563912349 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16803217 | AATTATCTCCAGCTG[A/G]CCTCGGCCTTGACCT | 284434 |
rs563940203 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16732285 | TTGGTTAGCATGGCA[A/G]GTGGTGTAGAAAAGT | 284434 |
rs563962729 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16773530 | TGTCTCATATAAATT[A/C]TTCTAATGAGCCCGA | 284434 |
rs563969018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16764197 | ATGCTGCTTAATACC[C/T]TACAGTGCACAGGAC | 284434 |
rs563969459 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16721902 | GATGGCTTGAGGCCA[A/C]GAGTTCAAGAACAGC | 284434 |
rs564003372 | snp | C/T | 0.125528 | 0.21681 | intron-variant | NWD1 | GRCh38.p7 | 19:16738630 | TTTTCTGAGATCTAT[C/T]TTCTGAGACCTAAAG | 284434 |
rs564004153 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16808828 | GCCAGGTGCAGTGGC[A/T]CACCCGGCACTTTGG | 284434 |
rs564092325 | snp | A/G | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16792192 | AGGGACTAGGAGTTG[A/G]GCTCTATCCACCTGC | 284434 |
rs564140727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16799793 | GATTACAGGCGTGAG[C/T]CACCGCGCCTGGCCC | 284434 |
rs564147231 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16791290 | CTTGCATTTGACTCC[A/G]GGAAACTTGTAGTCT | 284434 |
rs564222512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16806483 | CCAGTACTTTGGGAG[A/G]CAAAGGTGGGAGGAT | 284434 |
rs564224999 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16794380 | CAAAAACAAAAAAAA[A/T]AAAAATTAAAAAATT | 284434 |
rs564286644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16793637 | ACTGGAATGCAGTGG[C/T]GCAATCTCGGCTCAC | 284434 |
rs564343207 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16811023 | GGCATGTGCCACTGC[A/G]CCTGGCTAATTTTTT | 284434 |
rs564358961 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16755792 | ATCCTCCCACCTTGG[A/C]CTCCCAAAGTGCTGG | 284434 |
rs564366535 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16786095 | GTCTCGAACCCCTGA[C/T]CTCAACTGATTCACC | 284434 |
rs564374611 | in-del | -/CATC | 0.00280504 | 0.0373451 | intron-variant | NWD1 | GRCh38.p7 | 19:16754704 | ATCCATCATCTCTAG[-/CATC]CATCCATCCATCCAT | 284434 |
rs564381545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16799529 | TATTTTTTTTGAGAC[A/G]GAGTTTCATTCTTGT | 284434 |
rs564386374 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16761649 | ATCACAGGCATGAGC[A/C]ACTGCACCCAGCCTG | 284434 |
rs564428631 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16789390 | GATAATTCTTTCTGA[C/T]CCCAAGATTTGAAAC | 284434 |
rs564429665 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16792597 | TGAGGCAGGAGAATT[G/T]CTTGAACCTAGGAGG | 284434 |
rs564429992 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16785023 | GAAATGTCCAGAACA[C/G]ACTAATCCACAGAGA | 284434 |
rs564439087 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16759721 | ATCTCTACAAAAAAA[A/T]TAAGAAAATTAGCTA | 284434 |
rs564459593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16803409 | TTGGTGGGGGGGTGG[A/G]GACACAAATCTTCAG | 284434 |
rs564480109 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16742211 | GAAACCCTGTCTCTA[C/T]TAAAAATATAAAAAT | 284434 |
rs564494072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16754414 | TCCATCTATCCATCC[A/G]TCTATCCGCCCATCA | 284434 |
rs564513398 | snp | A/G | 1.64765e-05 | 0.00287019 | missense | NWD1 | GRCh38.p7 | 19:16789098 | AAATTTACCATTTGG[A/G]ATGGAGGCTCAAAAA | 284434 |
rs564519901 | snp | A/G | 3.31087e-05 | 0.00406857 | synonymous-codon, utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16797877 | GGGGTCCCTTGATGC[A/G]CTCATTCAGGTGAGG | 284434 |
rs564564172 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16725652 | CCGCCTCCCAGGTTC[A/C]AGCGATGCTTCCGCC | 284434 |
rs564584843 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16740112 | GACCAGCCTGGGCAA[C/T]GTAACAAGGCCCCAT | 284434 |
rs564603303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16804183 | GGCTCAGCTAAAGTC[C/T]CTCTCAGCATCATTC | 284434 |
rs564605734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16809957 | CACCCCTTTCTATCT[A/G]CCTGGTCACAGGGAG | 284434 |
rs564612937 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16785638 | TATATATATACACTT[A/T]TATATACATATTTTA | 284434 |
rs564613896 | snp | A/G/T | 6.60168e-05 | 0.00574497 | missense | NWD1 | GRCh38.p7 | 19:16762052 | CATGGCGTCCTGGCC[A/G/T]ACTTCTTCTCAGGGA | 284434 |
rs564650609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16754950 | TTCTCTATGTCCCAT[C/T]GATAAATATGTATAG | 284434 |
rs564655862 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16763283 | CCATCCAATCTGATT[A/G]TGATTATGCCTCTTG | 284434 |
rs564671904 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16720900 | CTGTTGCCCAGGCTG[G/T]AGCGCAGTGGCACGA | 284434 |
rs564680976 | snp | C/T | 0.000140756 | 0.00838797 | synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744441 | CATCGGTGATCAGTA[C/T]GGCCCCTGTCTGATT | 284434 |
rs564689012 | in-del | -/TCCA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764509 | TCATCCTTCTGTCTG[-/TCCA]TCCATCCATCCATCC | 284434 |
rs564764390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16795388 | GACCCTGAAGCCCCA[C/G]AGGGGGTGTTACAGT | 284434 |
rs564830006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16801159 | TGGTGCATGCCTGTA[A/G]TCCCAGCTACTCAGG | 284434 |
rs564858092 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16774642 | CCTTCCCATCCTTTC[A/G]TCCGTCCATCCACCC | 284434 |
rs564875769 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16775720 | GTCGCCCAGGCTGGA[C/G]TGCAGTGGCGCAATC | 284434 |
rs564896120 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16776425 | ATACAAAAATTAGCC[A/G]GGCGTTGTAGCGGAC | 284434 |
rs564916960 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16800655 | ATCTCGTGTCTGGTG[A/G]GGACCCGTTTCCTGG | 284434 |
rs564933736 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16745196 | ATTCCTTATAAAACC[A/G]TCAGATCTTGTGAGA | 284434 |
rs565009358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16757083 | TTGTAGAATTATTTC[A/G]TTATATATTGCAATG | 284434 |
rs565014643 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16750988 | GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAC | 284434 |
rs565043666 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16780286 | TCAGCCTCCCGAGTA[A/G]CTGGGACTACAGGCG | 284434 |
rs565085918 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16742210 | CGAAACCCTGTCTCT[A/T]CTAAAAATATAAAAA | 284434 |
rs565098380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16781564 | GGGGCTACAGTGAGC[C/T]GTGATTACACCACTG | 284434 |
rs565102651 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16725878 | TCTTGGGCTCATGCA[A/G]TCCTCCCATCTCAGC | 284434 |
rs565147082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16741554 | TTATATTTTTAATAG[A/G]TATGGGGTTTCGCTA | 284434 |
rs565150933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16746846 | AAACATAAGTGGATC[A/G]TCAGTCACAAAGGTC | 284434 |
rs565180976 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16740762 | CAGGTGTGAGCCACC[A/G]CACTGGCCCAGGTTA | 284434 |
rs565182663 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16768708 | ACCTGGGGCCTTAAA[A/T]ACCATGTTAACAAAG | 284434 |
rs565185514 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16793737 | ATGTGCCACCACGCC[C/T]GGCTAATTTTTGTAT | 284434 |
rs565211908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16746472 | GAGGTCAGGAGTTCA[A/G]GACCAGCCTGGCCAA | 284434 |
rs565218754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16751829 | AAGAGAAGGAAGGAA[A/G]GAAGGAAGGAAGATA | 284434 |
rs565250654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16774327 | CAAACCACTTTCCTC[C/T]CCATCCATCCATCCA | 284434 |
rs565307637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16780982 | ATTTTTTGATGGGAG[A/G]AGCTGCAAAGTCACA | 284434 |
rs565316687 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16719738 | GTCAGCAAATGGCAT[C/T]TTTTACGAGGAGCCG | 284434 |
rs565359413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16727958 | TCCCAGCTACTTGAG[A/G]GGCTGAGGCAGGAGA | 284434 |
rs565384985 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16727867 | AGAGTTGAAGACCAA[A/C/G]CTGGGCAACATGGCG | 284434 |
rs565424654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16733437 | GGGGCAGGAGAATTG[C/T]TTGAACCTGGGAGGT | 284434 |
rs565441516 | snp | A/G | 1.66551e-05 | 0.00288571 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807719 | TTCCAGGCAGGACGT[A/G]ATATGCATTCCCCCT | 284434 |
rs565475262 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16797558 | TCACCATGTTGGCCA[A/G]GCTGATCTCGAACTC | 284434 |
rs565480641 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16807392 | CAGCTACTCGGGAGG[C/G]TGCGGCAGGAGGATT | 284434 |
rs565480764 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16813740 | CCTCGGCCTCCCAAA[G/T]TGCTGGGATTAGAGA | 284434 |
rs565539680 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16808975 | CTGTGATCCAGCTAC[G/T]TGGAGGGCTGAGGCG | 284434 |
rs565611763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16729665 | CCTGAGGTGAGGAGT[C/T]TGAGACCAGCGTGGC | 284434 |
rs565659374 | snp | C/T | 1.65718e-05 | 0.00287848 | missense | NWD1 | GRCh38.p7 | 19:16765142 | CTGAGGTTGGCCTGG[C/T]CCGTGAAGCCCTCCA | 284434 |
rs565695089 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718491 | TATCTGAAACTTCTA[C/T]CCCTGAAAATATAGT | 284434 |
rs565695830 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16809200 | GCAACTCTCCCGCCT[C/T]GGCCTCCCAAGTAGC | 284434 |
rs565705889 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16745308 | CGTGTGAATTATGGG[A/C]GCTACAATTCAAGAT | 284434 |
rs565715635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16771032 | GGGCCGAGTGCGGGG[A/G]TTCACGCTTCTAATC | 284434 |
rs565778109 | snp | G/T | 0.093777 | 0.195178 | intron-variant | NWD1 | GRCh38.p7 | 19:16777597 | GAGGGGAGGGGAAAG[G/T]GGAGGGGAGGGGAAA | 284434 |
rs565817609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16723388 | ATTTTTTGTAGAAAT[A/G]GGGTTTCACCATGTT | 284434 |
rs565872748 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751242 | AAAAAAAAAAAAAAA[-/T]GCAATAAACTTGGGT | 284434 |
rs565889851 | snp | A/C/G/T | 0.000169843 | 0.009214 | intron-variant | NWD1 | GRCh38.p7 | 19:16797716 | AGAGGTGTAACCCCA[A/C/G/T]TTCCTGCCGTTTCAG | 284434 |
rs565902720 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16784177 | GCCACTGCACTCCAG[C/G]CTTGGTGACAGTGAG | 284434 |
rs565906344 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16719820 | CTAAGCTGGTGCCCT[A/G]GTGCAAACAATCGCT | 284434 |
rs565931347 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16742393 | AAAATAAAATAAATA[A/C]TAAATAAATAAATAT | 284434 |
rs565962648 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16795520 | CTCCCGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 284434 |
rs565968449 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16743420 | CACTATGTTGCCCAG[C/G]TAGTCTCTAACTCCT | 284434 |
rs565972073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16803618 | TAACTTCAATCAGGT[A/G]GAAACTAGCTAGTCA | 284434 |
rs566008788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16803079 | TGAGGAGCAAAGTCA[C/T]GTCTTACATGGTGGC | 284434 |
rs566009880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16809722 | ACCACGCCTGGCTAA[C/T]TTTTTTGTATTTTTT | 284434 |
rs566040389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16789646 | TTTTCTAATTAAATT[C/T]CATTTTGATGATGTA | 284434 |
rs566114556 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16776562 | GAAAGAGTAAAACTC[C/T]GTCTCACAAAAAAAA | 284434 |
rs566183340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16763418 | CATTTCCCACCCGCA[C/T]CCCCTAACCTGACTT | 284434 |
rs566225659 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16790329 | CACACTGTAAGCACC[A/G]AATAATTGATATCTA | 284434 |
rs566238785 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16802776 | GAGGCCAAGGCAGGC[A/G]CATCATTTGAGGTCA | 284434 |
rs566250199 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16784398 | GGTAACAATAGTAAT[A/C]AAGTATACAGGAGGA | 284434 |
rs566260095 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16805357 | CACCACTGTGCCCAG[A/C]CAAATTTTGTGTGTT | 284434 |
rs566266369 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16743738 | CCCAGGCTGGACTGC[A/C/G]GTGGCACCATGTCGG | 284434 |
rs566313781 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16783693 | AAAATAATAAAATAA[A/T]AAATAAATAAAAATA | 284434 |
rs566333564 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16739272 | TGAGATGAGAGGATC[A/T]CTTGAGCCCAGGAGT | 284434 |
rs566353757 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16745322 | GAGCTACAATTCAAG[A/G]TGAGATTTGGGTGAA | 284434 |
rs566383431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16752265 | GACCTTTGTCGGTTA[C/T]CACAAATTCATCTAG | 284434 |
rs566434431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16786309 | CACCTGGCCCAGTCA[C/T]ATCCTTGTTCTGTTA | 284434 |
rs566446139 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16808231 | CACCATGGGCCATCG[A/G]CCAGGATGGGACTGG | 284434 |
rs566483091 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16793106 | GAATCATCCCAAATC[C/G]CAAAGCTCCACATTT | 284434 |
rs566496451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16726689 | AGTGATCCACCCACC[C/T]CGGCCTCCCAAAGTG | 284434 |
rs566530468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16755271 | CCCAGACTGGAGTGC[A/G]CTGAAGCGATCACAG | 284434 |
rs566563600 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16785710 | GTAAAACATAATATA[C/T]ATGTGTGAATAAAAC | 284434 |
rs566569407 | in-del | -/AAAA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16739352 | AAAAAAAAAAAAAAA[-/AAAA]TTATTTTTTTAAGGA | 284434 |
rs566623162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16745160 | CAGGTAAGACAGAGT[A/G]AGAGCCAAGCGAAAG | 284434 |
rs566640744 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NWD1 | GRCh38.p7 | 19:16781107 | GTCCCTTAACAGATA[C/T]GGCTTATTTCTGTAA | 284434 |
rs566705662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16780409 | GATCCACCCACCTCG[C/T]CCTCCCAAAGTGCTG | 284434 |
rs566778813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16810330 | GTAATCCCGGCTACC[C/T]GGGAGGCCGAGGCAG | 284434 |
rs566808910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748856 | GAAGAAGAATAAGAG[C/T]AATGGCTTAACTAGT | 284434 |
rs566824124 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16740285 | GCCTGGGTGCCAGAG[A/G]AAGAGTCTGTCTCTT | 284434 |
rs566849918 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16792277 | TGGGCGCTGTGTCTC[A/C]CTCCTGTAATCCCAG | 284434 |
rs566867059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16744126 | GGGGACAGTGGCTCA[C/T]GACAGTAATCCCAGC | 284434 |
rs566885511 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16738612 | GGCCAGAGAGATATT[C/T]TATTTTCTGAGATCT | 284434 |
rs566896092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16775869 | GACAGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 284434 |
rs566956185 | snp | C/T | 0.376592 | 0.215579 | intron-variant | NWD1 | GRCh38.p7 | 19:16782865 | TCTTCCTTTTCCTTC[C/T]TTCTTTCTTTCTTTC | 284434 |
rs566958175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16775242 | TTGAGGATTCTAAGA[C/T]TGAAGCTAGCTTAGT | 284434 |
rs566986451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748455 | TCACTTTTTGAGGAT[A/G]ACAGCATTGTTTTAC | 284434 |
rs567006611 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817826 | GACCAATTAAGATTT[C/T]ACCTACAAATTCTGA | 284434 |
rs567011467 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16719261 | GTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 284434 |
rs567018572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16782141 | AATCTAACCCTTTTA[C/T]GTAATTAAGAAAACA | 284434 |
rs567048449 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16812687 | AAACAAACAAACAAA[C/G]AAACAAACAAACAAA | 284434 |
rs567052768 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16760779 | TATTTTTAGTAGAGA[C/T]GGGTTTCACCATGTT | 284434 |
rs567144994 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16801610 | AGTCCAAGCTACTTG[G/T]GAGGCTGTGGTGGTA | 284434 |
rs567159956 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16772575 | CGCTTGAACCTGGGA[C/G]GTGCAGGTTGCAGTG | 284434 |
rs567204486 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16737532 | AAAGTTCTGGGATTA[C/T]AGGCATAAGCCAATG | 284434 |
rs567214993 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16756292 | AAAAATACATGTACT[A/G]TTCATGAAGTGGAAG | 284434 |
rs567248418 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16783045 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTCAGGATC | 284434 |
rs567308022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16762344 | CTCTGTCGCCCAGGC[C/T]GGAGTGCAATGGCGT | 284434 |
rs567350719 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16789235 | AAAGCTGAGACCAGA[C/G]CATTCAAAGACAGAA | 284434 |
rs567400458 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16733129 | GGGAGGCTGAGGTGG[C/G]AGGATCACTTGAACC | 284434 |
rs567440214 | snp | A/G | 3.29761e-05 | 0.00406041 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16763890 | GAAGCTGAAGGAGTT[A/G]CCCTATCACCTGCTT | 284434 |
rs567458376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16769746 | GAAGCCTTGTCTGGC[C/T]ACCACTGAAGCTTAA | 284434 |
rs567472602 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16808321 | TTTGGAGGCTGAGGC[A/G]GGCGGATCACCTGAG | 284434 |
rs567484142 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16729475 | CCCTTCTCTGCCCCT[C/T]GATGTAAAGTAGATT | 284434 |
rs567493910 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16814292 | CCTAAGGTCACACAG[C/T]GAGTAACTAGTAGGC | 284434 |
rs567503043 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16770341 | TGCTCAGCTCTCATT[A/C]TTCTCTCTCCTCCCG | 284434 |
rs567511702 | snp | C/T | 0.00018185 | 0.00953372 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16815036 | CTTACAGGCACCCTG[C/T]TGACAGTCCAGTTTG | 284434 |
rs567512263 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16750667 | AGAGATAGGGGTCTG[C/G]CTCTGTCACCCAGGC | 284434 |
rs567522712 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16797603 | TCTGCCCGCCTTGGC[A/G]TCCCAAAGTGCTGGG | 284434 |
rs567533563 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16804245 | GTCTTAGTCAATTCC[A/G]GCCACTATAACAGAA | 284434 |
rs567602382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16768146 | ATTACAGGTGTGTGC[C/T]ACCACATGCAGCTAA | 284434 |
rs567612179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16812638 | CACACCACTGCACTC[C/T]AGCCTGGGCAACAAG | 284434 |
rs567641269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16756785 | GAGGTGAGCAGTGGG[C/T]GAACAAGTGAAGCTT | 284434 |
rs567683494 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16806915 | CCAGCTACCCGGGAG[A/C]CTGAGGTGGGAGAAT | 284434 |
rs567712926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16788757 | TTTCTGTTATTAGGC[A/G]TACAAGCGTGAGAAC | 284434 |
rs567773387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16774502 | CCATCCATCTATCCA[C/T]CTACCCTACCACTGT | 284434 |
rs567782568 | in-del | -/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16811982 | GATCAGGCTACTGCA[-/C]CTCAGCCTCAGGAAC | 284434 |
rs567858223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16736478 | ATTATACTGAGGTTA[C/T]GAATTTGGTTCAAGT | 284434 |
rs567877958 | in-del | -/AA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751240 | AAAAAAAAAAAAAAA[-/AA]TGCAATAAACTTGGG | 284434 |
rs567891184 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16774854 | CCATTCATTCACTTA[C/T]GCCTCCACCCATCCA | 284434 |
rs567940923 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16800568 | TATCCCCATAGACTG[C/G]GTGGCATAAGCAAGA | 284434 |
rs567949647 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16723357 | GTGTGCACCACCACA[A/T]CTGGCTAATTTTTAA | 284434 |
rs567966112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748548 | ATGGCTAAATCAGGC[C/T]GGGCGCAGTGGCTCA | 284434 |
rs567999572 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16719935 | TTGTCTTCCGGGTGG[C/T]GCCGAGGCCAGGAAA | 284434 |
rs568003801 | snp | A/C/G/T | 0.000362899 | 0.0134661 | missense, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800081 | CGCACCGGCCTCACC[A/C/G/T]CAGTGTCCCACAATG | 284434 |
rs568059986 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16725296 | GGCATGATCCACTGG[G/T]CCCAGACTCTACACA | 284434 |
rs568064774 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16764744 | CCGTGATTCTTAACC[A/G]GAAGAGATTCTGCCC | 284434 |
rs568096338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16765259 | GAAACATGCTCTCCT[C/T]ATTGAGTCATGAGCT | 284434 |
rs568133304 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16796970 | GATCACTTGAGATCA[G/T]GAGTTTGAGACCAGC | 284434 |
rs568195328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16796280 | ACTTCTGATGATCAT[A/G]GTGAAACCCTGTCTC | 284434 |
rs568202572 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16785866 | ATTGACTCTTTTTTT[A/T]AAATTTTTTTGTTTT | 284434 |
rs568247779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16802146 | AAAATTAGCCGGACG[C/T]GGTGGCGGGCACCTG | 284434 |
rs568262429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16792353 | TCGAGACCAGCCTGG[C/T]CAACATGGCAAAACC | 284434 |
rs568287852 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | NWD1 | GRCh38.p7 | 19:16760682 | TGCAACCTCTGCCTC[A/C]CAGGTTTCAGCGATT | 284434 |
rs568297896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16740792 | AACTCTTTTGGATTC[C/T]GGTTTGCACCTACTC | 284434 |
rs568316454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16735733 | TACTCAGGAGACTGA[A/G]GCATAAGAATCGCTT | 284434 |
rs568317572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16783933 | ATATACAGGAGTGGC[C/T]GGGCACAGTGGATCA | 284434 |
rs568380661 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16790332 | ACTGTAAGCACCAAA[G/T]AATTGATATCTATTT | 284434 |
rs568397934 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16790990 | TAATCCCAGCACTTT[A/G]AGAGGCTGAGCAGGG | 284434 |
rs568405169 | snp | C/T | 9.88826e-05 | 0.00703076 | missense, synonymous-codon | NWD1 | GRCh38.p7 | 19:16797779 | GACTCGAGGGGCTTT[C/T]GCCGATTCATGGCCA | 284434 |
rs568462419 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16752883 | TCACACCTGTAGTCC[C/T]AGCTACTCGGGAGGC | 284434 |
rs568470364 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16806982 | AGATTGTGCCACTGC[A/G]CTCCAGCCTGGACAA | 284434 |
rs568495674 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16757912 | CAAAAATTAGCCGGG[C/T]GTGGTGGTGCACACC | 284434 |
rs568519505 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16752346 | GAAATAGAAACACAT[G/T]CATGCTAGTGTAGGA | 284434 |
rs568529026 | snp | C/T | 0.000608651 | 0.0174343 | synonymous-codon, intron-variant | NWD1 | GRCh38.p7 | 19:16794543 | TGAAGATGAGTCCCT[C/T]CTCGCCGCAGGTAGC | 284434 |
rs568546885 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815945 | GGAAACTGAGCCTTG[C/T]GGAAGTAGTTATAAT | 284434 |
rs568582258 | in-del | -/AAT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16788236 | ACTTCATCTCAAAAT[-/AAT]AATAATAATAATAAT | 284434 |
rs568583115 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16735072 | CCCGACTAAATGTTT[A/G]TAAATAAACTTCTGA | 284434 |
rs568651155 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16799610 | CTCCCGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 284434 |
rs568663710 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16806198 | GTTTCTATACCTCTA[C/T]CCTCCCAGCAGGACT | 284434 |
rs568686494 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16742586 | GTCCTCTTAGCCCTG[C/G]TTCACCTCTGATTCT | 284434 |
rs568712950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16733183 | CTGTGATGGAGCCAC[C/T]GCACTCTAGCCTGGG | 284434 |
rs568740192 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16760593 | TTATTTATTTAATTT[A/T]ATTTTATTATTTTTT | 284434 |
rs568791465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16780459 | CCGTGCCCAGCCAAA[A/G]GCAGGGTTTCAAGAA | 284434 |
rs568797757 | in-del | -/AAAAG | 0.00244848 | 0.0349033 | intron-variant | NWD1 | GRCh38.p7 | 19:16808550 | ACTCCGTTTAAAAAA[-/AAAAG]AAAAGAAAAGAAAAG | 284434 |
rs568852745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16787121 | AATAGCTCTCTAAGA[C/T]TATTATATTTATTTA | 284434 |
rs568858133 | snp | A/G | 4.99039e-05 | 0.00499495 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750121 | CTACTGGGAGGTGAA[A/G]CCCCTTTCCGGAAAC | 284434 |
rs568863868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16769406 | GGCAGAGGTTGCAGT[A/G]AGCCGGGATCACACC | 284434 |
rs568871989 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | NWD1 | GRCh38.p7 | 19:16766364 | CTGTGATTGCTCCGC[-/T]GCATTCCAGCCTGGG | 284434 |
rs568876281 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16795195 | TTTTGGCCCAGCCCG[C/G/T]GGCTCCCATGGCCAC | 284434 |
rs568897141 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16756624 | ATAATCTATATGCCT[A/C]TCTATACATCTGCCT | 284434 |
rs568918132 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16728879 | AACCCAGGAGGCGGA[A/G]CTTGCAGCGAGCCGA | 284434 |
rs568937326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16772686 | AAACAAACAAATAAA[C/T]TAGCTGAGTGTGGTG | 284434 |
rs568939349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16779912 | AGTAGCTGGGATTAC[A/G]AATTTGAGCCACAAA | 284434 |
rs569001780 | in-del | -/TA | 0.0479149 | 0.147179 | intron-variant | NWD1 | GRCh38.p7 | 19:16738749 | ATATAATATATATAT[-/TA]TATATATATAATATA | 284434 |
rs569021231 | snp | A/G | 1.64741e-05 | 0.00286998 | intron-variant, splice-acceptor-variant | NWD1 | GRCh38.p7 | 19:16812744 | TGTCTGTTTTCAACA[A/G]AGTTCTTACTGCAGA | 284434 |
rs569036622 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16768251 | TCTGCCCACCTTGGC[C/T]TCCCAAAGTGCTGGG | 284434 |
rs569036915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16775031 | CTATTTATCTGCCCA[C/T]CCACAATCTCTCACA | 284434 |
rs569037553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16740856 | ATGGCCTCCCATGCC[C/T]TACAGAATCTTGTGC | 284434 |
rs569052285 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16726996 | GGAAGGACTTTGCCT[C/T]GTGGGAGGGGGTGGG | 284434 |
rs569064241 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16781955 | AAAAATTAGCTGGGC[C/G]TGATGGTGGGTGCCT | 284434 |
rs569083325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16745776 | AACAAAATTAGCTAG[A/G]TATAGTGGTGCATGC | 284434 |
rs569098541 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16774525 | ACCACTGTTTCATTT[A/T]TCTAGCCCCATTCAT | 284434 |
rs569255596 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16743258 | CTCTGTCCCCCAGGC[C/T]GGAGTGCAGTGGTGC | 284434 |
rs569276287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16731414 | CGGGTTCAAGCGATT[C/T]TCCTGCCTCAGCCTC | 284434 |
rs569276978 | snp | C/T | 0.0023264 | 0.0340263 | intron-variant | NWD1 | GRCh38.p7 | 19:16797927 | TCCTCACCTCCACCT[C/T]GGGAACAGACACTGA | 284434 |
rs569292949 | snp | A/T | | | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16719457 | GTTTTAATGGTAATT[A/T]ATCATGGCTAACATC | 284434 |
rs569298666 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | NWD1 | GRCh38.p7 | 19:16737577 | TTAAGTTTTTTTTTT[C/T]TTTTGAGATGGGTCT | 284434 |
rs569328621 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16761869 | CACAGGTGGTCAACA[C/G]AGTGGTTTAGGATGG | 284434 |
rs569338415 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16784862 | TGAACCCGGGGGGCG[A/G]AGGTTGCAGTGAGCC | 284434 |
rs569348517 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817526 | AGAATGGCTTGAACC[C/T]GGGAGGCGGAGGTTG | 284434 |
rs569359152 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16744138 | TCACGACAGTAATCC[A/C]AGCACTTTGTGAGGC | 284434 |
rs569360085 | snp | C/T | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817071 | TTTGGAAGGCCGAGG[C/T]AGGTGGATCACCTGA | 284434 |
rs569369668 | in-del | -/AAAAT | 0.0182019 | 0.0936463 | intron-variant | NWD1 | GRCh38.p7 | 19:16785514 | AGACTCTGTCTCAAA[-/AAAAT]AAAATAAAATAAAAT | 284434 |
rs569374306 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16805993 | CCTGCCTCAGCCTCC[C/G]TTCCAAGTAGCTGGG | 284434 |
rs569448665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16747183 | CTGGGATTACAGGCA[C/T]GCGCCACCTCGCCTG | 284434 |
rs569451403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16721046 | GTAGAGATGGGGTTT[C/T]GCCATGTTGGCCAGG | 284434 |
rs569491840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16727174 | AGGTTGGCTGGTCCC[C/T]GGGCCCCAATGCCCA | 284434 |
rs569537312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16766671 | GCTCACTGCAACCTC[C/T]GCCTATCAGGCTCAA | 284434 |
rs569540420 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16792407 | ATTGACCAGGCACGG[A/T]GGCTCACACCTGTAA | 284434 |
rs569546036 | in-del | -/AAAG | 0.00953873 | 0.0683987 | intron-variant | NWD1 | GRCh38.p7 | 19:16776950 | CTATCTGAAAAAAAA[-/AAAG]AAGAAGAAAAGGAAG | 284434 |
rs569551042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16726692 | GATCCACCCACCTCG[A/G]CCTCCCAAAGTGCTG | 284434 |
rs569553376 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16764383 | CATCCATCCATCCAT[C/G]CATCCATCCATCCAT | 284434 |
rs569582317 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16811279 | AAATTGAATCCCCAT[C/T]GAAAAAAGAAATTGA | 284434 |
rs569615160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16771017 | TAAGAGAGGGAGATG[A/G]GGCCGAGTGCGGGGG | 284434 |
rs569617029 | snp | G/T | 1.67192e-05 | 0.00289125 | intron-variant | NWD1 | GRCh38.p7 | 19:16763965 | GGGCTGCCCCCCATC[G/T]CAGAGGACCGAGCCT | 284434 |
rs569622057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16734357 | ATTGAGACCATCCTG[A/G]CTAACACGGTGAAAC | 284434 |
rs569643403 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16734899 | CCTCTGTTCTAATTT[G/T]TTTATTTTAATTAAC | 284434 |
rs569644254 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16776066 | TAGAATGACTATGGG[A/G]GCACAAATCGCACAT | 284434 |
rs569654279 | snp | A/C | 1.64741e-05 | 0.00286998 | utr-variant-3-prime, missense | NWD1 | GRCh38.p7 | 19:16815132 | TATCTGATCCGAGAG[A/C]ATTTCCAGTGCCTTT | 284434 |
rs569657860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16776523 | CAGTGAGCGGAGATC[A/G]TTCCACTGCACTCCA | 284434 |
rs569720812 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16814499 | AGGAGACTTGCCCAA[A/G]GTCACAAAACAAGTA | 284434 |
rs569747496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16807353 | ACAAAATTAGCTGGG[C/T]GTGGTGGCACACACT | 284434 |
rs569775111 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16794754 | CTGCAGTTGTGGTAC[-/A]TAAACTAGCATAGAC | 284434 |
rs569787947 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16719029 | TTTTTTTTGTAGAGA[C/T]GGGGTTTCACCGTGT | 284434 |
rs569846381 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NWD1 | GRCh38.p7 | 19:16772990 | AGAAGGAGACAGGAG[C/T]GGACAGCAGAGGCCA | 284434 |
rs569856927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16727774 | CTTTAAGAGACCTAG[A/G]CGTGAACCAAGTACT | 284434 |
rs569857319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16803004 | TGTAAAGGAAAGAGG[C/T]TTAATGGACTCACAT | 284434 |
rs569894070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16809142 | TCACCCAGGCTGGAA[C/T]GCAGTGGCGCCATCT | 284434 |
rs569900338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16808596 | ATTTGTCTCAGAAGC[A/G]AAGTTTTTTTTGTTT | 284434 |
rs569916029 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16746597 | AGAATCACTTGAACC[C/T]GGGAGGCAGCGGTTG | 284434 |
rs569926904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16757176 | CTACCCTGGTCCGCG[A/G]GAAAAAAATTGTCTT | 284434 |
rs569951696 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16800798 | TCACTTCCCTGTCAC[C/T]CTGCTACAGTTCGGA | 284434 |
rs569965996 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16722788 | GGGAGCTTTAAGTCA[C/T]GTGATATTGGTTGAC | 284434 |
rs569976540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16751324 | AGTCAAAAGTAACAA[A/G]CATATATTGCTTTTT | 284434 |
rs569991476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16762964 | AATTTTTGTATTTTT[A/G]GTAGAGACGGGGTTT | 284434 |
rs569999112 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16780440 | GGATTACAGGCGTGA[A/G]CCACCGTGCCCAGCC | 284434 |
rs570012960 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815692 | ATGCAGAGCTCTAAT[A/C]GGCTAGACTGATCCA | 284434 |
rs570037005 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16750736 | CAACTCCCAGGCTCA[A/G]GTGATCCTCCCATCT | 284434 |
rs570045035 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754693 | ATCTTCCATCCATCC[A/C]TCATCTCTAGCATCC | 284434 |
rs570100668 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16782925 | TTCTTTCCTTCCTTT[C/T]CTTCCTTCCTTCCCT | 284434 |
rs570113853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16722240 | GGAGATGGAGGCTGC[A/G]GTGAGCCACAATAGT | 284434 |
rs570180850 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16807109 | AGGAGAATCACTTGA[A/G]TCCAAAAGTTGGAGG | 284434 |
rs570196419 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16725961 | TTTTTTTTTTGTTTG[G/T]TTTTTTTTGCTTTTT | 284434 |
rs570276510 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16789425 | CATCTTTTTTGAATA[G/T]CAGCATTTTAGGGCT | 284434 |
rs570314449 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16798682 | CAGGCTGGAGGGCAG[G/T]GTGGCATGATCTCAG | 284434 |
rs570342398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16795470 | TGCGTAGGCTGTAGT[A/G]CAGTGGTATGATCTC | 284434 |
rs570343205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16757656 | GCCCGCTCTGAGGTT[C/T]GCATTGCTTAGGGGA | 284434 |
rs570353622 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16805321 | GCCTCGGCCTCCCAA[A/C]GTGCTAGGATTACAG | 284434 |
rs570360367 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787221 | AGCCTCAACCTCCTG[C/T]GCTCAAATGATCCTC | 284434 |
rs570362813 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16801459 | ACAAACAAAAAAGCC[A/T]GGCGTGATGGCTCAC | 284434 |
rs570363743 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16812429 | ATCCCAGCACTTTGC[A/G]AGACCAAGGCTAGTG | 284434 |
rs570422230 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815587 | TCAATAGAAAAGAGA[A/G]CTTCTCTTTCCCAAC | 284434 |
rs570424539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16792433 | TGTAATGCCAGCACT[C/T]TGGGAGGCCGGGGCA | 284434 |
rs570435320 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749030 | GGTGCACGTTAATCT[G/T]GAGAACCAATGCACA | 284434 |
rs570468802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16760715 | CCTGCCTTAGCTTCC[C/T]GAGTAGCTAGGTTTA | 284434 |
rs570567239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16765929 | GGCTGAGGCAGGAGA[A/G]TTGCTGGAACCTGGG | 284434 |
rs570572988 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16779513 | TTCCATAGTGAAAAG[C/T]TGGTTCTCAGAGCCC | 284434 |
rs570579766 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16780067 | TGGCTGAATCTGAAT[A/G]TTTTCAAATGAGGCA | 284434 |
rs570613501 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16786747 | AGACGGGGTTTTGCC[G/T]TGTTGGCCAGGCTGG | 284434 |
rs570651315 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16797093 | GCTGAGGCAGGAGAA[A/T]CGCTTGAACCCAGGA | 284434 |
rs570670856 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16755241 | TTGGGGGGGGACAGG[G/T]TCTCACTCTCTTGAC | 284434 |
rs570674091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16786239 | TCTCGGACTCCTGGG[C/T]TCAAGTGACCCTCCC | 284434 |
rs570696906 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16722234 | AGGACAGGAGATGGA[A/G]GCTGCAGTGAGCCAC | 284434 |
rs570723746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16809837 | GCTGGGATTACAGTC[A/G]TGAGCCACCGTGCCT | 284434 |
rs570732837 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16784209 | CTCAGTCTTAAAAAG[-/A]AAAAAAAAAAAAGAA | 284434 |
rs570735022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16792923 | GGTGGTGCATACTTG[C/T]ACTCCCAGCTACTTG | 284434 |
rs570775266 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NWD1 | GRCh38.p7 | 19:16784907 | GCACTCCAGCCTGGG[C/T]GATGACAGAGTGAGA | 284434 |
rs570779086 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16735489 | CCAGCCTGGGTGACA[A/G]AGCAAGACTCTGTCC | 284434 |
rs570856971 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748300 | GTTGATGGATGTTTG[G/T]ATTGTTTCTGTCTTT | 284434 |
rs570879247 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782356 | CTGAAGTCCCAGCTA[C/T]GTGAGAGGCTGAGCC | 284434 |
rs570900696 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16738312 | GGTGGCTCACTCCTG[C/T]AATCTCTGCATTTTG | 284434 |
rs570921187 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16788096 | TTTGCCAAGTGTGGT[C/G]GTGGGCACCTGTAAT | 284434 |
rs570938462 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16752904 | CTCGGGAGGCTGAGG[C/T]AGGAGGATTTGTTGA | 284434 |
rs570966338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16737375 | CTTCTGATCTCCCTG[C/T]CTTGTTCTCCCAAGT | 284434 |
rs570982799 | snp | C/T | 3.29658e-05 | 0.00405978 | intron-variant | NWD1 | GRCh38.p7 | 19:16779340 | GCCTCTGTGTGGCTG[C/T]AGGCATCACCGCCAT | 284434 |
rs571098200 | snp | A/G | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16736637 | TCTATTTCCCAGGTC[A/G]TTGATCTGAGGTGGG | 284434 |
rs571108533 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16727219 | TAGTTGCTATGGTGA[C/G]TACTGCGCTCTGAGG | 284434 |
rs571113974 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16778751 | TGACCTCAAGTGATC[C/T]GCCCACCTCGGCCTC | 284434 |
rs571163425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16813504 | GTTTTTGAGATGGAG[C/T]CTAGCTCTGTCACCC | 284434 |
rs571199738 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16743676 | TTTATTTATTTATTA[A/G]TTTGTTTATTTATTT | 284434 |
rs571214178 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748903 | TCCCTGGACCAGCAA[C/G]CCTTGGCTTGTTGCA | 284434 |
rs571256285 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16740069 | TGAGAGGCTAAAGCC[A/G]GAGGATCGTGTGATC | 284434 |
rs571256598 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16781275 | CCCACAGTAGAGTTC[A/G]TAACTAGCTACCTTG | 284434 |
rs571258255 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16746166 | GGAGACCAGTCTGGG[C/G]AACATGGCAAAACCT | 284434 |
rs571273348 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16767533 | GGTGGGAAAATTGCT[G/T]GAACACGGGCGGCAG | 284434 |
rs571275303 | snp | A/G | 0.000183082 | 0.00956594 | missense | NWD1 | GRCh38.p7 | 19:16750131 | GTGAAGCCCCTTTCC[A/G]GAAACCAAGGCCAGC | 284434 |
rs571278356 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16746743 | GTTCTATCTATCATA[C/T]CCTGTTTTCTTACAA | 284434 |
rs571318720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16794931 | GGATTACAGGCACAC[A/G]CCACCACACCCAGCT | 284434 |
rs571360991 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16728893 | AGCTTGCAGCGAGCC[A/G]AGATCATGCCACTGC | 284434 |
rs571386938 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16769680 | CTGGGACTCGCCTCC[C/G]CCAGCCCTTCTGTGG | 284434 |
rs571404302 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16783950 | GGCACAGTGGATCAC[A/G]TCTGTAATCCCAACA | 284434 |
rs571420369 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16779794 | AGCACATACCACTAT[A/G]CCCAGCTAATTTTTT | 284434 |
rs571431378 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16734166 | GCCAAACTAAACACC[C/T]TCCTTTGCAAGGAAA | 284434 |
rs571442860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16810293 | AAATACAAAAATTAG[C/T]CCTGCATGGTGGTAT | 284434 |
rs571462721 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16814382 | TCCTATAGAAAAGGC[A/G]CTCATTGTGTATTAT | 284434 |
rs571499565 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754374 | TCATCTCTATCATCC[A/T]TCCACCCATCATCTC | 284434 |
rs571581420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16773785 | TTCCATTCATCCAAC[C/T]ATCTATGCATCCATC | 284434 |
rs571612406 | snp | C/T | 6.66789e-05 | 0.00577365 | intron-variant | NWD1 | GRCh38.p7 | 19:16761965 | GTCTATCAGTCTGTA[C/T]ACCCTCTCTGTAGAC | 284434 |
rs571684084 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16811964 | GAGGTTGCAGTGAGC[A/C]GAGATCAGGCTACTG | 284434 |
rs571705748 | snp | C/T | 0.000627464 | 0.0177014 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16773280 | AGGATTCCTCCAGCC[C/T]CCGGGAGGACCCCTC | 284434 |
rs571711020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16794604 | CTAATCAGGATCAGG[C/T]TGGAGAAGGGGGTGG | 284434 |
rs571728096 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16756728 | CCATCCCCCAGTACC[A/G]GTACTGCTCCGTGGC | 284434 |
rs571755673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16758098 | AGTGTTGGGTATGAC[A/G]TTATTACCAATATGG | 284434 |
rs571771231 | snp | A/G | 3.29717e-05 | 0.00406015 | synonymous-codon, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800056 | CCGGGTGCCTGCACC[A/G]TTTCTGGACCGCACC | 284434 |
rs571808302 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16818093 | AGGATCACTTGAGCC[C/T]AGGAGTTTGAGACCC | 284434 |
rs571852089 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16756103 | AAGAAAATCATAAAG[C/G]GGGGCTGGGCATGGT | 284434 |
rs571872969 | in-del | -/G | 0.00517822 | 0.0506191 | intron-variant | NWD1 | GRCh38.p7 | 19:16726891 | CGTGGCAACTGGAAA[-/G]GTCTCCAGACATTGC | 284434 |
rs571892773 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16727662 | CCATCTTCATCAGTT[C/T]CACAGTCTCAGGTAA | 284434 |
rs571894777 | snp | C/T | 0.139225 | 0.224118 | intron-variant | NWD1 | GRCh38.p7 | 19:16799667 | ATGCACCACCAAGCC[C/T]GGCTAATTTTTTGTA | 284434 |
rs571921909 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16805217 | GTGTGCAGCACAATG[C/T]CTGGCTTATTTTTGT | 284434 |
rs571925934 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16751833 | GAAGGAAGGAAGGAA[A/G]GAAGGAAGATAGTAA | 284434 |
rs571929094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16783977 | AACACTTCGGGAGGC[C/T]GCGGATCACCTGAGG | 284434 |
rs571935504 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16806170 | GAGTCACCACGCCCT[G/T]CCATTAACAGGAGTT | 284434 |
rs571954503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16795871 | TTCCCTCTGCCATCA[A/G]GGACAGAGGGCCACA | 284434 |
rs571959050 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16806783 | ATTTTGGGAGGCCGA[A/G]GCGGGCGGATCACTT | 284434 |
rs571984725 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16775750 | CTCGGCTCACTGCAC[A/C]TCTGCTTCCCAGATT | 284434 |
rs572001664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16801877 | AACTCTGTTAGTTCT[C/T]GCGAGGTTGTTAAAA | 284434 |
rs572009255 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16778830 | ATGAGCCACCGTGCC[C/T]GGCCATGGCCAATGT | 284434 |
rs572016278 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16727226 | TATGGTGACTACTGC[A/G]CTCTGAGGACGAGGA | 284434 |
rs572048045 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16802518 | TCTCTCTTGCTTCCT[C/T]TGGCCGTATGACCTC | 284434 |
rs572080392 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16724274 | CAAGGTGGATATTTT[C/T]GGCATTAATTTTGAT | 284434 |
rs572100385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16746292 | GTCAGCCTAGGAGGC[A/G]GAGATTGCAGTGAAC | 284434 |
rs572103355 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16776810 | AGCTGGTCATGGTGG[C/T]ATGTGCCTATAGTCT | 284434 |
rs572140036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748032 | TCTGTTGCACAGGCT[A/G]AAGTGCAGTGACATG | 284434 |
rs572163017 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16746045 | CCAAAACGTAACTAC[G/T]AATAGCCCACCAATC | 284434 |
rs572168737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16791280 | GAGAAGGCATCTTGC[A/G]TTTGACTCCGGGAAA | 284434 |
rs572191866 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16741723 | GACTCCCCAGGCTAC[A/G]TACGACCCATGTTTT | 284434 |
rs572212780 | snp | C/T | 3.29533e-05 | 0.00405901 | missense | NWD1 | GRCh38.p7 | 19:16807991 | GTGCAACTTCCAAAG[C/T]GTTTCCCTTGGAGAC | 284434 |
rs572234066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16809377 | CTGCACCTGGCCAAG[A/G]AGTAATATTTTAATG | 284434 |
rs572234449 | snp | C/T | 0.000278862 | 0.0118048 | synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16731263 | CTTCTGCCAGAGGCA[C/T]GGCTTGATGTTTGAG | 284434 |
rs572237187 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16737603 | GGTCTTGCTATGTTG[C/T]CCAGGCTGGCCTGAG | 284434 |
rs572260207 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16742730 | GGCTGGAGTGCAATG[A/G]CGCAATCTCGGCTCA | 284434 |
rs572319273 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732101 | CATGCCTGTAGTCCC[-/A]AGCTACTCAGGAGGC | 284434 |
rs572322463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16752593 | CTGCAGTAAGCCATA[A/G]TTGTGCCACTGGGCT | 284434 |
rs572329426 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16769057 | AAAGCCCAAAACGGC[C/T]GGGGTGGCTCAAGCC | 284434 |
rs572361560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16741996 | GGCGCCTGTAGTCCC[A/G]GCTACTGGGGAGGTA | 284434 |
rs572373171 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16741068 | GGGAGGCTGAGGCAG[A/G]AGAATCACTTGAATC | 284434 |
rs572419188 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718708 | TTGTTTTTTGTTTTT[C/T]ATGTAGAGACAGGGT | 284434 |
rs572459423 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16750952 | CTAGGCCAGGCGTGG[C/T]GGCTCACACCTGTAA | 284434 |
rs572465277 | snp | C/G/T | 0.000253926 | 0.0112653 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750292 | ATGGGCCTCTTTCAC[C/G/T]GTGCCTGTCCCGCTG | 284434 |
rs572485558 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16795100 | TTTCTTTCCTTTTGA[G/T]GCAGGATTTTTCTTG | 284434 |
rs572516950 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16739784 | TAGAGAGGCTCCTGT[C/G]TCTTGGGCTATCAGC | 284434 |
rs572544021 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16728665 | TTAAGTAATTGCAGG[A/C]CGGGTGCAGTGGCTC | 284434 |
rs572547827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16800885 | TAAACCTATAATCAC[A/G]GCACTCTGGGAGGCC | 284434 |
rs572552623 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16788333 | CCAGCACTTGGGAGG[C/T]TCAGGTGGGTGGATC | 284434 |
rs572558157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16743966 | GGGATTACAGGTGTG[A/G]GCCACCGCGCCTGGC | 284434 |
rs572571126 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16769841 | TCTTGGCTCTTTTTC[C/T]TTTTTCTTTTTTTAG | 284434 |
rs572579479 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16814607 | ACACTATTATACATT[A/G]TAGTATAATATGCTG | 284434 |
rs572584964 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16769368 | TCGGGAGGCTGAGGC[A/C]GGAGAATTGCTTGAA | 284434 |
rs572596096 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16734466 | CGTGAACCCGGGAGG[C/T]GGAGCTTGCAGTGAG | 284434 |
rs572618132 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16733998 | GGCAGGGACTGTTCC[A/G]AGTTGTCTTTGTCTC | 284434 |
rs572633069 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16776191 | TTCTGTGTTTCAGAT[A/C]CACTGTGCCCCGCTG | 284434 |
rs572638458 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16720542 | CTGCCCCCTAGGGGA[C/T]ATTGCAATGTCTAGG | 284434 |
rs572649610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16775476 | TCCTCGTTGGCCCAA[C/T]ATAGCTGCTCCAACT | 284434 |
rs572742836 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16744218 | ATGTAGTGAGACCCT[A/T]TCTGTACCGAAAATA | 284434 |
rs572744117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16813831 | CGTGTCTCTTGGTCT[A/G]TTCAGTATTATGCTA | 284434 |
rs572769122 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NWD1 | GRCh38.p7 | 19:16731557 | TGATCTGCCCGCCTC[A/G]GCCTCCCAAAATGCT | 284434 |
rs572776739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16783091 | TGCTGGAGCACAATG[A/G]TGCAATCATAGTACA | 284434 |
rs572832467 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16737744 | TTTGGGAGGCCAAGG[C/T]GGGTGGATCATGAAG | 284434 |
rs572834260 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16779738 | AAACTCCTGGGCCAA[C/G]TGATCCTCCTGCCTC | 284434 |
rs572883827 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16809445 | CATGAAGAACAAAAT[C/G]TCAACATTATAGGTA | 284434 |
rs572896643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16798227 | GTAGATGGTGAAATA[A/G]CAGATCTTCAGTGTT | 284434 |
rs572911108 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748678 | AAAATACAAAAATTA[G/T]CCAGGCGTGCTAGTG | 284434 |
rs572958228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16785380 | GTTGGGCATGGTGGC[A/G]CATGTCTGTAATCCC | 284434 |
rs572995154 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16778133 | ATTCTCAGAGCTTGA[C/T]GGGCTCTGATTCAGC | 284434 |
rs572996367 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16754833 | CCACACATCATCTCT[A/G]TCTTCCCTGCATCCA | 284434 |
rs573022803 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16818149 | ATTTTTTTTTAATTA[G/T]CTGGGCATGGTGGTG | 284434 |
rs573028908 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16799599 | GCAAACTCCACCTCC[C/T]GGGTTCAAGCGATTC | 284434 |
rs573064762 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16810652 | CCTGTAGTCCCAGCT[A/T]GTTAGGAGGCTGAGG | 284434 |
rs573129045 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16771949 | TACAGGCCTGCGCGC[A/C]ACCATGCTCGGCTAA | 284434 |
rs573153884 | in-del | -/AAAAG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16808549 | ACTCCGTTTAAAAAA[-/AAAAG]AAAAGAAAAGAAAAG | 284434 |
rs573176046 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16719561 | AACACAGGAAGTTAG[C/T]GAGAAAATTCAAGTG | 284434 |
rs573225845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16771258 | GGAGTTTGAGACCAG[C/T]CTTGGTGACAGTGAA | 284434 |
rs573245450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16803339 | ACCAACAGACTTAGA[C/T]AGGCCCCAGCTCCTA | 284434 |
rs573248844 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16764776 | CCCAGGGGACACTTG[A/G]CAATGTCTGCAGACA | 284434 |
rs573298671 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16810689 | GATCGATTGAGCCCT[A/G]GAGTTCGAGGCTGTA | 284434 |
rs573334633 | in-del | -/ATCCATCC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754498 | TCCATCCATCCATCC[-/ATCCATCC]ATCATCTCTATCTTC | 284434 |
rs573398769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16774645 | TCCCATCCTTTCATC[C/T]GTCCATCCACCCACC | 284434 |
rs573405314 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16743346 | CTCCTGAGTACCTGA[A/G]ACTACAGATGCACAC | 284434 |
rs573430816 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16761689 | TTCTTAATTCTCGGT[A/G]TATACCCAGGAGTGG | 284434 |
rs573458718 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16754186 | ATCTATCCATCATCT[C/T]GATCTTCCATCCTTC | 284434 |
rs573516543 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16810157 | AGAAAGCCATGTAAG[A/G]CTGGGCACCATGGCT | 284434 |
rs573522132 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16725041 | TTTTGAGACGGGGTC[A/T]CACTCTGTCGCCCAG | 284434 |
rs573525479 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | NWD1 | GRCh38.p7 | 19:16733338 | CCAGCCTGGCCAACA[A/T]GGTGAAACCCCCTCT | 284434 |
rs573525831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16760006 | TCAAAAAAAAGAAAA[C/T]TAGCTGGGTGTGATG | 284434 |
rs573555306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16769054 | TTGAAAGCCCAAAAC[A/G]GCCGGGGTGGCTCAA | 284434 |
rs573582184 | snp | G/T | 0.0014043 | 0.0264608 | splice-acceptor-variant | NWD1 | GRCh38.p7 | 19:16731191 | ATGCCCTTCCTTGCA[G/T]ATATGGATGCAGAGA | 284434 |
rs573626281 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800390 | AATACAAAAGTTAGC[C/T]GGGCATGGTGGCACA | 284434 |
rs573675904 | in-del | -/TATC | 0.00478085 | 0.0486577 | intron-variant | NWD1 | GRCh38.p7 | 19:16754896 | TCCACCCATCCGTCA[-/TATC]TATCTATCTATGTCT | 284434 |
rs573733874 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16796805 | CTAGTTTCTGAGATA[A/C]CATGATGAGCCAAAT | 284434 |
rs573747488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16733297 | AGGCCAAGGCGGGTA[A/G]ATCACCTGAGGCCAG | 284434 |
rs573759926 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16773824 | CACCTTCCTACTCTT[C/T]CATCCAATTACCCTC | 284434 |
rs573806035 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16761516 | AGCACACCACCACGC[A/C]CAGCTAATTTTTGTA | 284434 |
rs573810543 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | NWD1 | GRCh38.p7 | 19:16740220 | GGGAAAATCCCTTGA[A/G]CCCAGAAGTCTGAGG | 284434 |
rs573848867 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | NWD1 | GRCh38.p7 | 19:16774198 | ATCCATCTATCCTCC[C/T]ACCCTTCCATCCATC | 284434 |
rs573850740 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16781420 | CAGGATTTTGAGACC[A/G]GCTTGGGCAACATGG | 284434 |
rs573854717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16722983 | GCCATACAACTTCAC[C/T]GGGAGGGGACGACTG | 284434 |
rs573891257 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16763124 | CTTCTCCCCCCGAGA[A/C]CCATTCACAAATCCT | 284434 |
rs573930653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16757359 | CCTCACTTCCTCCTC[C/T]GCATGGAGGGGCTGG | 284434 |
rs574029014 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16721101 | GTAATCTGCCTGTTT[A/T]GGCCTCTCAAAGTGC | 284434 |
rs574090465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16726853 | TGGTCTCCACCCACG[C/T]GATGCCAGTAGCATC | 284434 |
rs574140184 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16806311 | TACTCCTGGGAATTG[C/T]CCACTGATGAAAGAA | 284434 |
rs574150158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16799219 | TTATTTTTATTTTGA[C/T]GGAGTCTCACTCTGT | 284434 |
rs574194289 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16788125 | ATCCCAGCTACTCGA[C/G]AGGCTGAAACAGGAG | 284434 |
rs574204056 | snp | A/G | 0 | 0 | intron-variant | NWD1 | GRCh38.p7 | 19:16745359 | GCCAAACCATATCAG[A/G]GGGAGCAATGCAGGG | 284434 |
rs574229818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16787463 | CTGATTGACTCCCAA[C/T]CAGTTGTGGCCCTCT | 284434 |
rs574230087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16805577 | TCTCAAGCCATCCTC[C/T]CACTTCAGCCTCCTG | 284434 |
rs574243005 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16771358 | GGGAGGCTGAGGCAC[C/G]AAAATTGCTTGAACC | 284434 |
rs574266944 | snp | C/T | 8.47077e-05 | 0.00650743 | missense, intron-variant | NWD1 | GRCh38.p7 | 19:16749894 | GTGGTCCAGTTTTTC[C/T]ATACCCTCCTCCACA | 284434 |
rs574272670 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16739656 | TCTGATTTGTGGGGG[C/T]GCCTTCCACAAAAAT | 284434 |
rs574280526 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16725473 | GCAGAGCAAGACTCT[C/G]TATCACCTAACAACA | 284434 |
rs574295741 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16794223 | ATACAAAAATTAGCC[C/G]GGCATGGTGGCAGGT | 284434 |
rs574310031 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16778199 | AAGGAAAAGGACTTC[C/T]TTTCTTTACTCCAGG | 284434 |
rs574404547 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748129 | GTTGGGATTACAGGC[A/G]TGCGGCATCACGCTG | 284434 |
rs574418991 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16758644 | GGTGCAGTTGGTTTC[C/T]GCATTATTTTCCTTG | 284434 |
rs574421970 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16727602 | GCCGGCGGCTTCTGC[A/G]GGGTGAAGCCGGCCC | 284434 |
rs574454195 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718763 | TTGATCTCCTGACCT[C/T]GTGATCTGCCTGCCT | 284434 |
rs574488680 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732316 | GAGTAGGAGTGAATG[C/T]TTTTGAACACAGATT | 284434 |
rs574518158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16724314 | CATTGCACTACCTCA[C/T]ATATTGCTGCAGAGA | 284434 |
rs574553654 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16735921 | GTGAGACAAGATTGC[A/G]CCACTGCACTCTAGC | 284434 |
rs574591326 | snp | C/T | | | utr-variant-3-prime, synonymous-codon | NWD1 | GRCh38.p7 | 19:16815125 | GCATGGTTATCTGAT[C/T]CGAGAGAATTTCCAG | 284434 |
rs574625503 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16733477 | AGTGAGCCGAGATAA[C/T]GCCACTGCACTCCAG | 284434 |
rs574633795 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16795574 | GGCACCTGCTACCAC[A/G]TCCCGCTAATTTTTG | 284434 |
rs574655907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16784668 | GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 284434 |
rs574674993 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16736219 | CCTTCTTTCCTTCCT[A/T]CCTTCCTACCTTCCT | 284434 |
rs574683133 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816183 | TGGAAGGCAGAGATT[A/G]TGTCTAGGGTGGGTA | 284434 |
rs574697358 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16729790 | AGGAGAATCCCTTGA[A/G]TCTGGTAGGCGGAGG | 284434 |
rs574718998 | snp | A/G | 8.34509e-05 | 0.00645898 | intron-variant | NWD1 | GRCh38.p7 | 19:16791321 | AGGTCTCCTGCCAAG[A/G]TGCTGCTTCCTCTTC | 284434 |
rs574728653 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16770463 | AACCTCTTTCCTTTA[A/T]AAATTACCCAGTTTC | 284434 |
rs574754450 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16735109 | AATTTAGGCTTACAG[A/G]AAACGCATGGACAGT | 284434 |
rs574762455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16805692 | AAGCACCTCGAGAAT[C/T]GTAACCTCACTTGAT | 284434 |
rs574763602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16742100 | AGTAAATAGGCCAGG[C/T]GCAGTGGCTCATGCC | 284434 |
rs574827018 | snp | A/G | 0.000872895 | 0.0208731 | missense | NWD1 | GRCh38.p7 | 19:16791431 | TGGATGTGCATGGCC[A/G]TGCTGGCCTCCCAGG | 284434 |
rs574828163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16746680 | CTGTCTAAAAACAAA[A/G]AACAAAAAACAACAA | 284434 |
rs574836771 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16776290 | ATATGAAAAGTATGG[A/C]CAGGCATGGTGGCTC | 284434 |
rs574848050 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16723045 | CCTTGGATGCCTCTT[C/T]CTGTGCCTGATCTTA | 284434 |
rs574942833 | in-del | -/T/TGT/TGTT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16741369 | GTTTTGTTTTTGTGT[-/T/TGT/TGTT]TTTTTTTTTTTTTTT | 284434 |
rs574999803 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16751690 | CCTGTAATCCCAGCT[C/G]CTTGGGAGGCTGAGG | 284434 |
rs575043260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16814829 | CAATCTTAAAAATCG[C/T]CCTGAGCAGGTGTAG | 284434 |
rs575167641 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16726960 | CTGCTGGTTGAAATA[C/G]TATGTGCGGTGCCTG | 284434 |
rs575167769 | in-del | -/AG | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16793915 | AAATTTTTTAGAGAC[-/AG]AGTCTCAGTCTGTCA | 284434 |
rs575189714 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16732100 | CTCATGCCTGTAGTC[C/G]CAGCTACTCAGGAGG | 284434 |
rs575211683 | snp | C/T | 0.000164704 | 0.0090733 | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744779 | CACGTGTTCAGAATA[C/T]CCATCCCCTGTTGGC | 284434 |
rs575215285 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16729376 | CCCTGGGGCCCATAT[C/T]AGGACTATCACTCTC | 284434 |
rs575225927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16786441 | AATGATCCCATCACT[A/G]AGGTAGTGAGCATGG | 284434 |
rs575243416 | in-del | -/TTTTTTTTTTTTT | 0.459914 | 0.13578 | intron-variant | NWD1 | GRCh38.p7 | 19:16767168 | GGAAAGAGGTGCGTC[-/TTTTTTTTTTTTT]TTTTTTTTTTTTTTG | 284434 |
rs575258658 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16737832 | TAGCTGGGCATGGTG[G/T]CACGTGCCTGTAATC | 284434 |
rs575266519 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16773434 | TGTGCTAGTTGGGAG[C/G]CCCCAAGCTTGCCAT | 284434 |
rs575294671 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16730196 | GTGTGGTGGTGCACG[C/T]CTGTAATCCCAGCTA | 284434 |
rs575310279 | snp | A/G/T | 8.24877e-05 | 0.00642167 | missense | NWD1 | GRCh38.p7 | 19:16762043 | GCCAAGAGGCATGGC[A/G/T]TCCTGGCCGACTTCT | 284434 |
rs575322875 | snp | C/G | 0.000141213 | 0.00840158 | intron-variant | NWD1 | GRCh38.p7 | 19:16744418 | TGACTTCCTCTCTGC[C/G]AGGCCCTCATCGGTG | 284434 |
rs575332863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16806422 | ACAAAAGTCTGGCCC[C/T]CTTGCTTCAAGATGG | 284434 |
rs575335262 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NWD1 | GRCh38.p7 | 19:16786085 | GGCCAGGCTAGTCTC[A/G]AACCCCTGACCTCAA | 284434 |
rs575403847 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16721225 | CTAGTGGGTGGGGGC[C/T]GGAAATGCTTTGCAA | 284434 |
rs575421957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16812238 | GCTTGAAACCAGGAG[A/G]TGGAGGTTGCAGTCA | 284434 |
rs575435644 | snp | C/T | 6.62767e-05 | 0.00575621 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749384 | CGCCTGCCGTGGAGC[C/T]GCGACTTGGTGAACC | 284434 |
rs575446680 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16805744 | AGCTTTGCCTAGTGG[G/T]CTGTTACTCTAAAAA | 284434 |
rs575497528 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16798321 | GTTTTAAAGAAATTG[A/T]TAAATAGACTGTGCA | 284434 |
rs575535194 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16801279 | GCAAAACTCTGTCTC[-/A]AAAAAAAAAATTAGC | 284434 |
rs575536505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16767673 | CATGAGAACAGCATG[A/G]GGGAACCACCCCCAT | 284434 |
rs575558256 | snp | A/G | 0.00271965 | 0.0367754 | synonymous-codon, utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16797862 | CAACCTGATCATCAC[A/G]GGGTCCCTTGATGCG | 284434 |
rs575560562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16760058 | TACTTGGGAGGCTGA[A/G]GTGGGAGGATCACTT | 284434 |
rs575608235 | in-del | -/T | 0.0952156 | 0.196321 | intron-variant | NWD1 | GRCh38.p7 | 19:16761534 | CTAATTTTTGTATTC[-/T]TTTTTTTTAGTACAG | 284434 |
rs575662363 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16769812 | TTCTATCACTGCACC[C/G]TGTTTTCCATCTGTC | 284434 |
rs575772891 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16731130 | AAAATAAAAGCAGAG[C/G]TATGAGGCTGGGAAG | 284434 |
rs575780720 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16812930 | GTCCTGGGCATTAGA[G/T]GGCCCTGCTCTGGCC | 284434 |
rs575833371 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16796355 | TAATCCCAGCTACTC[A/G]GGAGGATGAGGTGGG | 284434 |
rs575896025 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16804928 | CTCCTGGGCTCAAGC[A/G]ATCTTCCTGCCTCAG | 284434 |
rs575915168 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16757458 | TCAGAAAAAGAGGAA[C/G]TAGTGCATTTTCTTC | 284434 |
rs575917737 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16786672 | CTGCCTCAGCTTCCC[A/G]AGGAGCTGGGATTAC | 284434 |
rs575940399 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | NWD1 | GRCh38.p7 | 19:16745565 | ACACCTCATCTCTAC[-/A]AAAAAAAAAAAAAAA | 284434 |
rs576075443 | snp | C/G | 0.00013428 | 0.0081928 | missense | NWD1 | GRCh38.p7 | 19:16749992 | CCGCCATGCTCGGAG[C/G]GTTCCCTGGCTGCCT | 284434 |
rs576117964 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16783469 | ATGAAACTCTGTCTC[C/T]ACTAAAAATACAAAA | 284434 |
rs576142526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16752489 | AGTGAGGCCCCTGTC[C/T]ATACAACAATTTTTT | 284434 |
rs576177022 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16728611 | TGTATATGTGCTCTC[A/G]TAGAAATTACATCCT | 284434 |
rs576182794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16768489 | TAACTTTTTGAGGAA[C/T]GACCACTTCATTTTC | 284434 |
rs576184573 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16733759 | ATGCCCGTCCTCTGA[C/T]GCGGATGCTGTCAAC | 284434 |
rs576237351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16727923 | AAAAATTAGCTGGGC[A/G]TAGTGGTGGGTGCCT | 284434 |
rs576243227 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16813711 | TGAACTCCTGACCTT[C/G]GGTGATCCACCCACC | 284434 |
rs576246062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16774652 | CTTTCATCCGTCCAT[C/T]CACCCACCCTTCCAT | 284434 |
rs576269273 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718030 | TTTTTTGTTATTGTT[A/G]TTGTTGTAGAGATGA | 284434 |
rs576286589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16746727 | AACACATATTTTGCA[C/T]GTTCTATCTATCATA | 284434 |
rs576312168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16801773 | TGGAGGGAGGCCTCA[C/T]GGGAGGTGTTTGAGT | 284434 |
rs576322915 | snp | A/G | 0.000936106 | 0.0216143 | intron-variant | NWD1 | GRCh38.p7 | 19:16762142 | TTGGACCGAAAGGTG[A/G]GGTACCTGGGACCCC | 284434 |
rs576349875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16745970 | ACCCTTGAACAACAT[A/G]GTGTTTAGGGACTCT | 284434 |
rs576412800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748566 | GCGCAGTGGCTCACG[C/T]CTGTAATCCCAGCAC | 284434 |
rs576420653 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16761609 | CTCAGGTGATGCACC[C/T]GCCTCAGCCTCCCAA | 284434 |
rs576421856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16756809 | GAAGCTTCATCTGTA[C/T]CTACAGCCACTTCTT | 284434 |
rs576560206 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16733413 | GTAATCCCAGCTACT[C/T]GGGAGGCTGGGGCAG | 284434 |
rs576569787 | snp | A/G | 3.64697e-05 | 0.00427007 | intron-variant, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800211 | GTAAGGCTTGGAGCC[A/G]TCTGTCTTAGTTTAG | 284434 |
rs576570685 | in-del | -/ACCCTCTAAAAAAGGTTTACAGGGC | 0.0134861 | 0.0810011 | intron-variant | NWD1 | GRCh38.p7 | 19:16798976 | GTTTTGAGCTTCCAG[-/ACCCTCTAAAAAAGGTTTACAGGGC]ACCCTCTAAAAAAGG | 284434 |
rs576622254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16740313 | CTTAAGAAAAAAAGA[A/G]GAAAAAAGAATAGAA | 284434 |
rs576639333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16781546 | GCTTGAGCTCAGGAG[A/G]TTGGGGCTACAGTGA | 284434 |
rs576655275 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16719590 | TGCAGAGTAGTGAAG[C/T]GTCACAGGCAAGGGA | 284434 |
rs576749209 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16743913 | GTCTTGAACTCCTGA[C/T]CTCAGGTAATCCACC | 284434 |
rs576850705 | snp | A/G/T | 3.29572e-05 | 0.00405928 | missense | NWD1 | GRCh38.p7 | 19:16797783 | CGAGGGGCTTTCGCC[A/G/T]ATTCATGGCCATGGA | 284434 |
rs576856479 | snp | A/G | | | missense | NWD1 | GRCh38.p7 | 19:16759304 | GTGTACCGAGATTGG[A/G]CCCCGCCCAGCAAGG | 284434 |
rs576869248 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16759864 | CCAGACGCGGTGGCA[C/T]GTGCCTGTAATCCCA | 284434 |
rs576876615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16753256 | TATTTCTGTGACCAG[A/G]TGCCATCTTACTGAC | 284434 |
rs576891808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16803692 | GAGGCTGAGGTGGGC[A/G]GATCATTTGAGGTCA | 284434 |
rs576918705 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16719464 | TGGTAATTAATCATG[A/G]CTAACATCTCACGGG | 284434 |
rs576923725 | snp | C/T | | | utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16720148 | AAAGAGAAACAGTTG[C/T]GGAGGAAGCTGTTGT | 284434 |
rs576934088 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16772783 | GAGGCTGCAGTTAGC[G/T]TTGATCATGCCACTG | 284434 |
rs576950895 | snp | C/T | 0.00013419 | 0.00819005 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749603 | CAGGAACTCCTGGCC[C/T]GGCTTGGGCAGCAGC | 284434 |
rs576962774 | snp | C/G | 0.000399281 | 0.0141238 | synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16731233 | CAGAGCACTGCCTAC[C/G]CTGAAGTGCCAGACC | 284434 |
rs576997869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16779609 | GTTGCATAATGAACC[A/G]TCCCCAAACACAGTA | 284434 |
rs577024011 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16736966 | AAATGGAAGCAGCAG[G/T]TGGCTTGGAGAGTAG | 284434 |
rs577074964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16809354 | GCTGGGATTACAGGT[C/T]TGAGCCACTGCACCT | 284434 |
rs577087503 | in-del | -/TTTTTT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16767189 | TTTTTTTTTTTTTTT[-/TTTTTT]GGTGAGACAGAGTCT | 284434 |
rs577091426 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16809959 | CCCCTTTCTATCTGC[A/C]TGGTCACAGGGAGAC | 284434 |
rs577091922 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817551 | AGGTTGCAGTGAGCC[A/G]AGATCGCACCACTGC | 284434 |
rs577093068 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16724394 | TGCCCTGGGAGGGAG[A/G]CCACTTGCTTAAGTC | 284434 |
rs577178886 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817066 | AGCTCTTTGGAAGGC[C/T]GAGGCAGGTGGATCA | 284434 |
rs577182851 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16776720 | GATCTCTTGGGCCGA[A/G]ATGTTCAAGACCAGC | 284434 |
rs577207852 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16785923 | AGGCTGGAGTGCAAT[G/T]ACATGATCTTGGCTC | 284434 |
rs577224644 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NWD1 | GRCh38.p7 | 19:16734608 | TTGCAACAGGGTGTC[A/G]CTCTGTCACCCAGGC | 284434 |
rs577229025 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16742641 | GGAGAACCACCACAA[A/G]ATTTAATTTAAATCT | 284434 |
rs577244694 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16783965 | GTCTGTAATCCCAAC[A/G]CTTCGGGAGGCCGCG | 284434 |
rs577263378 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16770636 | GCCCCACAGCCCTCA[G/T]TTTTCCCATCTGCAG | 284434 |
rs577263810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16776383 | GACCAGCCTGGCCTA[C/T]ATGGTGAAACCCTGT | 284434 |
rs577267544 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16807380 | CACTTGTAATCCCAG[A/C]TACTCGGGAGGCTGC | 284434 |
rs577286512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16742148 | GGGAGGCTGAAGCAG[A/G]CGGATCACCTGAGAT | 284434 |
rs577328938 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16793682 | CCCAGCTTCAAGCGA[G/T]TCTCCTGCCTCCGCC | 284434 |
rs577336005 | snp | C/T | 1.98785e-05 | 0.0031526 | missense | NWD1 | GRCh38.p7 | 19:16759352 | CCCCTGCTGTGGGTG[C/T]GGCTTCGTCGGGATC | 284434 |
rs577395811 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16759068 | GGGTATTGCCCTAAC[C/G]GTGCTTGGTACCTTG | 284434 |
rs577436847 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | NWD1 | GRCh38.p7 | 19:16747382 | TTATTTATTTATTTA[A/T]TTAATTTTTTTTGAG | 284434 |
rs577442476 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NWD1 | GRCh38.p7 | 19:16730332 | TCTCAAAAAACAAAC[C/T]AACAAAAAAACAAAA | 284434 |
rs577469767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16807215 | ATATGAACACCAGGC[C/T]GGGTGTGGTGGCTCA | 284434 |
rs577505767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16808935 | CAAACAAATGCAAAA[A/G]TTAGCTGGGCATGGT | 284434 |
rs577537244 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16774565 | CATCCGTTATTCATC[A/G]ATTCATCAAATCATT | 284434 |
rs577542652 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16764762 | AGAGATTCTGCCCCC[A/C]CAGGGGACACTTGAC | 284434 |
rs577591267 | in-del | -/A | 0.00716266 | 0.059414 | intron-variant | NWD1 | GRCh38.p7 | 19:16787292 | CCACCCCACCTGGCT[-/A]ATTATTTTTTTGCAA | 284434 |
rs577598290 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16774079 | ATCCATCCATCCACC[A/G]TCCTCCCACCCACCC | 284434 |
rs577605010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16771190 | GGCACAGTGGCTCAC[A/G]CCTGTAACCCCAATA | 284434 |
rs577611509 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16724240 | ACCTATCTCCCAACC[A/G]CCTTGTTGATGTTTT | 284434 |
rs577663206 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NWD1 | GRCh38.p7 | 19:16780650 | CTTTCTCTTCTCTTT[C/T]CTTTTCTTTTTCTCA | 284434 |
rs577681053 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NWD1 | GRCh38.p7 | 19:16767797 | ACCCATATCTCTCCC[A/C]ATTCTCCCTTCACCC | 284434 |
rs577770710 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800271 | GGGCCCCATGGCTCA[C/T]GCCTGTAATCCCAGG | 284434 |
rs577771738 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16739528 | CAACCGGCCCTGGGA[A/C]CTTCCAGAAAGGCCC | 284434 |
rs577833790 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16798823 | GTAGAGACGGGGTTC[C/T]GCCATGTTGGCCAGG | 284434 |
rs577838264 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NWD1 | GRCh38.p7 | 19:16794140 | GGAGGCCAAGGTGGG[C/T]GGATCACCTGAGATC | 284434 |
rs577840298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16786622 | TCCAGTCTTGGCTCA[C/T]TGCAACCTCTGCTTC | 284434 |
rs577894970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16727551 | ATCTTGGTGGGTGGG[C/T]GGCAATGAGCGTGGG | 284434 |
rs577902242 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NWD1 | GRCh38.p7 | 19:16793300 | GTGCAGTGGCACGAT[C/G]ATGGCTCCCTGCAGC | 284434 |
rs577944219 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787013 | ATGTGCCTTCCAACT[A/G]CAGTTTATCCTCCTG | 284434 |
rs577950900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16754971 | ATATGTATAGTCTCA[A/G]TCTATCTCTATCACT | 284434 |
rs577957086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16762512 | ACGTTGGCCATACTG[A/G]TCTCGAACTCCTGCC | 284434 |
rs577996049 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16813729 | TGATCCACCCACCTC[A/G]GCCTCCCAAAGTGCT | 284434 |
rs578006080 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16769324 | AAAATTAGCCAGGCA[C/T]GGTAGCACGCACCTG | 284434 |
rs578095112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16780232 | GCAATCTCGGCTCAC[C/T]GTAAGCTCTGCCTCC | 284434 |
rs578109150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16811354 | TTTGGGAGGCTGAGG[C/T]GGGTGGATCACTTGA | 284434 |
rs578142025 | snp | C/G/T | 1.66081e-05 | 0.00288163 | synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749503 | TGAGCTGGATACGGC[C/G/T]GGACAGGAGTTGGCG | 284434 |
rs578191244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16755474 | GCTCACTGCAACCTC[C/T]GCCTCCTAGGTTCAA | 284434 |
rs578216252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16768076 | AGCTCACCGCAACCT[C/T]CACCTCCTGGGTTGC | 284434 |
rs578221721 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16799027 | AAGGTTTACAGGGCA[A/C]CCTCCAGGAGTTCCC | 284434 |
rs578225144 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16766438 | AACTTATTTCTAGCT[C/G]CCAGATGACTTGGGC | 284434 |
rs578261116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NWD1 | GRCh38.p7 | 19:16721085 | GAACTCCTGGCCTCA[A/G]GTAATCTGCCTGTTT | 284434 |
rs745306543 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16756229 | TGCACTTGAGCCTGG[A/G]TGACAGAGCAAGACT | 284434 |
rs745309606 | snp | C/T | 1.65425e-05 | 0.00287593 | intron-variant | NWD1 | GRCh38.p7 | 19:16765030 | CCCCCCTTCTCTCCC[C/T]CAGGCAGCATGAGCT | 284434 |
rs745325239 | snp | C/T | 1.78864e-05 | 0.00299046 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750376 | ACACGGGCAGCTCCT[C/T]GTGGCCCACGTGCTG | 284434 |
rs745370637 | snp | C/T | 1.66228e-05 | 0.0028829 | missense | NWD1 | GRCh38.p7 | 19:16807735 | ATATGCATTCCCCCT[C/T]CCGAGGCCCGGAAAG | 284434 |
rs745399114 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16784885 | AGTGAGCCGAGATCG[C/T]GCCACTGCACTCCAG | 284434 |
rs745407245 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16798663 | CAAGTCTCACTCAGT[C/T]GCCCAGGCTGGAGGG | 284434 |
rs745437156 | snp | A/G | 2.25594e-05 | 0.00335845 | intron-variant | NWD1 | GRCh38.p7 | 19:16750430 | AGTCTCTGTGTTTTG[A/G]AACTCTTATTTATTT | 284434 |
rs745455946 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16811482 | CCAGCTACTTGGGAG[A/G]TTGAGGCAAGAGAAT | 284434 |
rs745477786 | in-del | -/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16808442 | TAATCTCAGCTACTT[-/G]GGGGGGCTGAGGCAG | 284434 |
rs745488114 | snp | A/G | 1.73048e-05 | 0.00294144 | synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749665 | CCTGGTACTCTTTGG[A/G]CCCCCAGGCATTGGA | 284434 |
rs745495090 | snp | C/T | 0.000140637 | 0.00838444 | intron-variant | NWD1 | GRCh38.p7 | 19:16736620 | TCTGACAAACTTGTG[C/T]TTCTATTTCCCAGGT | 284434 |
rs745500082 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16726123 | ATGCACCACCAAACC[C/T]GGCTAATTTTGTATT | 284434 |
rs745543001 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16721666 | TGGGTTTATGGGGGC[A/G]GGGTCCGTGGAGGAG | 284434 |
rs745549948 | snp | C/T | | | missense | NWD1 | GRCh38.p7 | 19:16797744 | CAGGCTTTGGAAGAT[C/T]GGTGCGGATATTCTT | 284434 |
rs745554199 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16745731 | GGTTACAGAGAGAGA[A/C]CTGTCTCAAAAAACA | 284434 |
rs745610229 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16762807 | TTCCTTCCTTCCTGA[C/G]AGAGTCTTGCTCTGT | 284434 |
rs745611487 | snp | C/T | 8.40838e-05 | 0.00648343 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16749977 | TGACCTGGACTCTGT[C/T]CGCCATGCTCGGAGG | 284434 |
rs745614490 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16793956 | CAATGCAGTGGCACA[A/G]TCATAGCTCACTGCA | 284434 |
rs745620126 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16750478 | TTATTTTTAGAGATG[C/G]AGGTCTGGCTATGTC | 284434 |
rs745650745 | snp | C/T | 1.64749e-05 | 0.00287005 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16789019 | ATTTGCCAAAGGGAC[C/T]CTCGCCAACTCTGCT | 284434 |
rs745655453 | snp | A/G | 6.85483e-05 | 0.00585401 | missense, upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749163 | GGGAGATAGAGCGGA[A/G]CCTGCTGAGCTCAGA | 284434 |
rs745659555 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16774831 | CATTTTCTTCATCTG[A/T]TCATCTTCCATTCAT | 284434 |
rs745665071 | in-del | -/G | 1.66012e-05 | 0.00288103 | frameshift-variant | NWD1 | GRCh38.p7 | 19:16763944 | GAAACAGGAGGTTCT[-/G]GGTAAGGGCTGCCCC | 284434 |
rs745669518 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16806734 | TAAATACATAAATAG[A/G]CTGGGCGCGATGGCT | 284434 |
rs745703708 | snp | C/T | 9.91457e-05 | 0.0070401 | missense | NWD1 | GRCh38.p7 | 19:16763915 | CTGCTTCACTCGGGC[C/T]GCCTGGAGGAGCTGA | 284434 |
rs745744489 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16766775 | ATATTTTGTAGAGAC[A/G]GGATTTTGCCATGTT | 284434 |
rs745828642 | snp | A/G | 5.08634e-05 | 0.00504273 | intron-variant | NWD1 | GRCh38.p7 | 19:16763990 | GAGCCTGGTGACTGC[A/G]CCACGCTCCAGTCTT | 284434 |
rs745835973 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16746193 | ACCTCACCTTTATTT[A/T]AAAAAAAAAAATTAA | 284434 |
rs745863168 | in-del | -/CCCACA | 0.000306984 | 0.0123854 | cds-indel, intron-variant | NWD1 | GRCh38.p7 | 19:16749867 | CCCAGGTTCTGGACG[-/CCCACA]CCCACACCAGGGTGG | 284434 |
rs745864956 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787045 | AGTTTTACATTTCTA[C/T]ATAATCCAGTTGGTC | 284434 |
rs745876162 | snp | A/G | 1.65658e-05 | 0.00287795 | intron-variant | NWD1 | GRCh38.p7 | 19:16773105 | AATCCAGGCAACTTA[A/G]TCTACATCCCTTTGT | 284434 |
rs745880715 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16773780 | CTTCCTTCCATTCAT[C/T]CAACCATCTATGCAT | 284434 |
rs745888923 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16791131 | CCCAGCTTCTTGGGA[A/G]GCTGAGGCAGGAGGA | 284434 |
rs745891356 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16769411 | AGGTTGCAGTGAGCC[A/G]GGATCACACCACTGC | 284434 |
rs745902258 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16743751 | GCGGTGGCACCATGT[C/T]GGTTCACTGAAACCT | 284434 |
rs745912469 | snp | A/G | 1.66037e-05 | 0.00288125 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749498 | CTCCGTGAGCTGGAT[A/G]CGGCCGGACAGGAGT | 284434 |
rs745960102 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16781910 | ATCCTGGCTAACACG[G/T]TGAAACCCTGTCTCT | 284434 |
rs746011876 | snp | C/T | 3.19392e-05 | 0.00399607 | missense | NWD1 | GRCh38.p7 | 19:16759385 | GGATACTACTTGGCC[C/T]GGCGGCCCGTGGATG | 284434 |
rs746027154 | snp | C/T | 1.65625e-05 | 0.00287766 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16773217 | GCTATGCCAACAGGC[C/T]CAGAGCTGGTTCCAG | 284434 |
rs746049236 | in-del | -/AAG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751425 | AGAAAGGAAGAGTGA[-/AAG]AAGGAAAGGAAGGAA | 284434 |
rs746057769 | snp | A/G | 1.64751e-05 | 0.00287007 | missense | NWD1 | GRCh38.p7 | 19:16807972 | GACCTCTTTCTTTAC[A/G]AGTGTGCAACTTCCA | 284434 |
rs746062382 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16742825 | ACAGGCATGTGCCAC[C/T]ATGCCTGGCTATTTT | 284434 |
rs746083204 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16752976 | GCACTCCAGTCTGGG[A/C]AACAGAGCAAGACCC | 284434 |
rs746085341 | in-del | -/GAAG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751821 | AAAGAGAAAGAGAAG[-/GAAG]GAAGGAAGGAAGGAA | 284434 |
rs746146063 | snp | A/G | | | missense, utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16799922 | GGGACCCTTCTGGAC[A/G]TCCTGGAAGGCGTCG | 284434 |
rs746154776 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16770530 | TACACACAGAGACCA[C/T]AAATTTTGAGCCCCA | 284434 |
rs746175020 | snp | C/T | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748420 | AGTGGAATTGCTGGG[C/T]GTGATAGTAACTCCA | 284434 |
rs746224130 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16775834 | CACCATGCCTGGCTA[A/G]TTTTTGTATTCTTGG | 284434 |
rs746259440 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16802668 | CTCTTATTCATAATT[A/G]TGCATTACTGTATTA | 284434 |
rs746265706 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16789313 | GGTGTAAATGGAGTA[C/T]ACAACCACTTGAGAG | 284434 |
rs746295724 | snp | C/G | 1.64781e-05 | 0.00287033 | missense | NWD1 | GRCh38.p7 | 19:16791492 | TGGTCAGTCTGTGGA[C/G]CTCAGCTACGGGAAA | 284434 |
rs746347563 | snp | G/T | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16747782 | CTCTATTAATTTGCC[G/T]GTTCTGGACATTTCA | 284434 |
rs746353201 | snp | A/C | 1.65737e-05 | 0.00287864 | synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749419 | GAACAAGACTCACGC[A/C]TGCTACCTGAAGGAG | 284434 |
rs746368248 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16730003 | GTGTTTTCAATAGCA[C/T]TCTTCACAAACTGCA | 284434 |
rs746413757 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16770675 | TGCTGAGTGACCATC[C/T]CACCTAGGGCTGCTG | 284434 |
rs746425352 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16758147 | ACTATGGAACACTTG[A/C]AAGGTGCTTCACACA | 284434 |
rs746443295 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16776305 | CAGGCATGGTGGCTC[-/A]ACGCCTGTAATCCCA | 284434 |
rs746473346 | snp | C/T | 3.30289e-05 | 0.00406366 | missense | NWD1 | GRCh38.p7 | 19:16763910 | ATCACCTGCTTCACT[C/T]GGGCCGCCTGGAGGA | 284434 |
rs746476992 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754402 | CTCTATCTTCCATCC[A/G]TCTATCCATCCGTCT | 284434 |
rs746494106 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16797580 | CTCGAACTCCTGACC[C/T]CGAGTGATCTGCCCG | 284434 |
rs746521507 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16796334 | GGGCATGGTGGCAGG[C/T]GCCTGTAATCCCAGC | 284434 |
rs746536392 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16810322 | ATGTGCCTGTAATCC[C/G]GGCTACCCGGGAGGC | 284434 |
rs746569078 | in-del | -/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16750910 | CTTAGCCTAGTAAAA[-/G]GTCTCGGAGCTATAA | 284434 |
rs746573085 | snp | A/C/G/T | 0.000101796 | 0.0071337 | missense | NWD1 | GRCh38.p7 | 19:16750303 | TCACCGTGCCTGTCC[A/C/G/T]GCTGGCCACCACCGC | 284434 |
rs746574203 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16724792 | CTGCCTCCCAGGTTC[A/G]AGTAATTCTCCTGCC | 284434 |
rs746594838 | snp | C/T | 5.17773e-05 | 0.00508782 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807671 | CCTATTTACGGGCCT[C/T]GTGTCGGGGGTCGTC | 284434 |
rs746626131 | snp | C/T | 3.32314e-05 | 0.0040761 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749517 | CCGGACAGGAGTTGG[C/T]GTGGCTCTACCAAGA | 284434 |
rs746626487 | snp | C/T | 7.04325e-05 | 0.00593391 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750364 | CCTGGAGCAGACACA[C/T]GGGCAGCTCCTCGTG | 284434 |
rs746630673 | in-del | -/C | 1.73447e-05 | 0.00294483 | frameshift-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749787 | AAATGAGCTCAGATG[-/C]CCGTGGCCTGCTGAA | 284434 |
rs746641269 | in-del | -/CCAT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764467 | ATGAGCTGGTTATAA[-/CCAT]CCATCCATCCATCCA | 284434 |
rs746648153 | snp | G/T | 2.15348e-05 | 0.0032813 | missense, intron-variant | NWD1 | GRCh38.p7 | 19:16794486 | CAAAGGGGACAGATT[G/T]CTGGAGAAGCTTCCA | 284434 |
rs746678087 | snp | C/T | 3.32751e-05 | 0.00407878 | missense | NWD1 | GRCh38.p7 | 19:16807729 | GACGTGATATGCATT[C/T]CCCCTCCCGAGGCCC | 284434 |
rs746703385 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16778357 | CAATTCATTGGCAAA[C/T]ATATATTTTTTTTCT | 284434 |
rs746734816 | snp | A/T | 4.78126e-05 | 0.00488917 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16759372 | TCGTCGGGATCTGGG[A/T]TACTACTTGGCCCGG | 284434 |
rs746758620 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16809034 | GCTCTCTAGCCTGGG[C/T]GATAGAGCAAGGCCT | 284434 |
rs746786353 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16784208 | CTCAGTCTTAAAAAG[-/A]AAAAAAAAAAAAAGA | 284434 |
rs746815336 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16772208 | CCGTCTCTACAAAAA[A/G]TAAAAAACTAACGAG | 284434 |
rs746832189 | snp | A/G | 1.65132e-05 | 0.00287339 | intron-variant | NWD1 | GRCh38.p7 | 19:16779471 | GGACACACAGGTGAG[A/G]CTTGGGAAGTGGGCT | 284434 |
rs746957344 | snp | C/T | 6.59576e-05 | 0.00574234 | utr-variant-3-prime, synonymous-codon | NWD1 | GRCh38.p7 | 19:16815050 | GCTGACAGTCCAGTT[C/T]GTCCATGCTGTGGTA | 284434 |
rs747025814 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16768414 | CTGTGGACATTTGTG[C/T]GTTTCTACCTTTTGG | 284434 |
rs747041548 | snp | A/C | 4.96709e-05 | 0.00498327 | synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749350 | CACTGACATGCACCC[A/C]GGGGTCCTCAAGACC | 284434 |
rs747043480 | snp | G/T | 1.67618e-05 | 0.00289493 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750184 | AGCTGCAAGGAGGAC[G/T]CTGAGCCCGGTGCAC | 284434 |
rs747066741 | in-del | -/AAAAG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16737970 | CTCTATCTCGAAAAG[-/AAAAG]AAAAGAAAAGAAAAG | 284434 |
rs747070861 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16741512 | CTGGGATTACAGGCA[C/T]CTACCACCATGCCCG | 284434 |
rs747072077 | snp | G/T | 1.64754e-05 | 0.00287009 | missense | NWD1 | GRCh38.p7 | 19:16791479 | TCCAGGGATGGTGTG[G/T]TCAGTCTGTGGAGCT | 284434 |
rs747088842 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16811969 | TGCAGTGAGCCGAGA[C/T]CAGGCTACTGCACCT | 284434 |
rs747114733 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16793680 | CTCCCAGCTTCAAGC[A/G]ATTCTCCTGCCTCCG | 284434 |
rs747161487 | snp | A/C | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816713 | GTGGCTATCCCTTCT[A/C]CCCTCCGTGGAATTC | 284434 |
rs747169719 | snp | A/G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16792310 | CTTTGGGAGGCTGAG[A/G/T]GGGGGTGGATCATTT | 284434 |
rs747193259 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16806657 | TTGAGGCTGCAGTGA[G/T]CCATGTTCGTGCCAC | 284434 |
rs747198769 | in-del | -/GA | 1.6656e-05 | 0.00288578 | frameshift-variant, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800125 | TTCCCCAAAATTGGG[-/GA]GACAAAAACAAAGTC | 284434 |
rs747239630 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16733896 | TCCTCCCCCTTTCTT[C/T]CTCCAGTCACATTGA | 284434 |
rs747246183 | snp | A/G | 1.64768e-05 | 0.00287021 | missense | NWD1 | GRCh38.p7 | 19:16807873 | GATGGGCCAAGATAC[A/G]CCTTTTACACTCAGC | 284434 |
rs747257632 | snp | C/T | 8.30089e-05 | 0.00644186 | intron-variant | NWD1 | GRCh38.p7 | 19:16773089 | AGGGTAGAGGGGGCT[C/T]AATCCAGGCAACTTA | 284434 |
rs747274562 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16761195 | GCAGGGATCAGTGCT[C/T]CCTTCCTTTTCATGG | 284434 |
rs747279362 | snp | A/G | 1.64972e-05 | 0.00287199 | missense | NWD1 | GRCh38.p7 | 19:16759286 | GACGAGGTCCTGCAG[A/G]ATGTGTACCGAGATT | 284434 |
rs747342502 | snp | C/T | 6.59185e-05 | 0.00574064 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16779350 | GGCTGCAGGCATCAC[C/T]GCCATGGCATGGGGT | 284434 |
rs747349100 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16756524 | TATCTATTTATCTAT[C/T]ATCTGTCTATTTATC | 284434 |
rs747361062 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16757626 | GGCGGGTCCTCTGGG[A/C]GTGCCAAGTGAGGTG | 284434 |
rs747367075 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16740333 | AAAGAATAGAAAAGA[A/C]ATTATTATTATTATT | 284434 |
rs747367214 | snp | A/C | 6.60289e-05 | 0.00574544 | intron-variant | NWD1 | GRCh38.p7 | 19:16812699 | AAACAAACAAACAAA[A/C]AAAAAACCCAAGAAA | 284434 |
rs747371238 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16774400 | TACCTTTCCATCCAT[C/T]TATCCCCCATCTCTA | 284434 |
rs747392538 | snp | A/C | 0.000156678 | 0.00884956 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744569 | ACGAGAATGCGTTTC[A/C]TCCCACCTACGTCCT | 284434 |
rs747397168 | snp | C/T | 9.91555e-05 | 0.00704045 | synonymous-codon, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800104 | CCACAATGGAAGCTA[C/T]GTCTACTTCCCCAAA | 284434 |
rs747448339 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16812921 | CTGACCTGGGTCCTG[A/G]GCATTAGAGGGCCCT | 284434 |
rs747463381 | snp | C/T | 1.6473e-05 | 0.00286988 | intron-variant, missense | NWD1 | GRCh38.p7 | 19:16812827 | TAAAGGATCGCTCTA[C/T]ACTTGTTTGGAGTGT | 284434 |
rs747474265 | snp | C/G | | | synonymous-codon, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800014 | CTCATCTTTCAAGGT[C/G]TGGGATCTCAGCGAT | 284434 |
rs747476193 | snp | A/C/G | 3.30105e-05 | 0.00406256 | missense, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800093 | ACCGCAGTGTCCCAC[A/C/G]ATGGAAGCTACGTCT | 284434 |
rs747481835 | snp | A/G | 3.32646e-05 | 0.00407814 | stop-gained | NWD1 | GRCh38.p7 | 19:16750112 | CCCGGAGGCCTACTG[A/G]GAGGTGAAGCCCCTT | 284434 |
rs747502296 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16742235 | TAAAAATTAGCCAGG[A/C]GTGGTGGCTCACGCC | 284434 |
rs747529859 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16726543 | CTCCTGAGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 284434 |
rs747608531 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16736979 | AGGTGGCTTGGAGAG[C/T]AGAATGTTGAAGCCA | 284434 |
rs747617391 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16763683 | CTCCAGCCCTGACCA[A/G]TGGGCACATGGGGGT | 284434 |
rs747635658 | snp | A/C/G | 0.000148539 | 0.0086168 | missense | NWD1 | GRCh38.p7 | 19:16807787 | GCAAGTGCGAGGACC[A/C/G]CCTGGCCATCGCCTA | 284434 |
rs747657483 | snp | A/G | 0.000439271 | 0.0148136 | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16745047 | GTAATTTACAAAGGA[A/G]AGAGGTTTAATGGAC | 284434 |
rs747667046 | snp | A/G | 1.64792e-05 | 0.00287042 | intron-variant | NWD1 | GRCh38.p7 | 19:16812872 | CATTTTGCTTTTAGG[A/G]CAGGATTGAGCTTCG | 284434 |
rs747676821 | snp | C/T | 3.29924e-05 | 0.00406142 | intron-variant | NWD1 | GRCh38.p7 | 19:16788966 | ATATACTCTCCCCTA[C/T]CCTGGCCTGCTGCAG | 284434 |
rs747688865 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16808871 | GGAGGATCACTTGAG[A/G]CCAGGAGCTGGAGAC | 284434 |
rs747723357 | snp | C/T | 1.65743e-05 | 0.00287869 | intron-variant | NWD1 | GRCh38.p7 | 19:16763810 | GTCCAAGCTGCAGTC[C/T]CCCTTCTCCTCTGCC | 284434 |
rs747757480 | snp | C/T | 0.000126166 | 0.00794148 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807608 | ACAAGATTCCCTGGA[C/T]ACCTCCAGTGAGATC | 284434 |
rs747774584 | snp | A/C | 3.35649e-05 | 0.0040965 | missense | NWD1 | GRCh38.p7 | 19:16750200 | CTGAGCCCGGTGCAC[A/C]CAGATTTGCTCTGGG | 284434 |
rs747793939 | snp | C/G | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748199 | ATGTTGGCCAGGCTG[C/G]TCTCAAACTCCTGAC | 284434 |
rs747814937 | snp | A/G | | | missense | NWD1 | GRCh38.p7 | 19:16789114 | ATGGAGGCTCAAAAA[A/G]TCCCGCTGAACCTCA | 284434 |
rs747829447 | snp | A/G | 3.29723e-05 | 0.00406018 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16763884 | CCTGCGGAAGCTGAA[A/G]GAGTTGCCCTATCAC | 284434 |
rs747848859 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16747652 | TGCTGAGATTACAGG[C/T]ATGAACTACACCTGG | 284434 |
rs747895324 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16774937 | TCCTCCATCTACCCA[A/T]CTACCTGCCCATCCA | 284434 |
rs747918339 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16784665 | GCTGGGCGCGGTGGC[C/T]CACGCCTGTAATCCC | 284434 |
rs747925060 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16797444 | CAAGCAATTCTCCTG[C/T]CTCGGCCTCCTGAGT | 284434 |
rs747931175 | snp | A/G | 3.29766e-05 | 0.00406045 | missense | NWD1 | GRCh38.p7 | 19:16807808 | CCATCGCCTATGACA[A/G]CATCGTCCTGGTGCT | 284434 |
rs747941945 | snp | C/T | 0.000148511 | 0.00861589 | missense | NWD1 | GRCh38.p7 | 19:16797762 | TGCGGATATTCTTGG[C/T]GGACTCGAGGGGCTT | 284434 |
rs747964422 | snp | A/G | 1.64912e-05 | 0.00287147 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16759276 | GTCCCTGGACGACGA[A/G]GTCCTGCAGGATGTG | 284434 |
rs748043520 | snp | C/T | 8.6737e-05 | 0.00658491 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749766 | TGCGGCTGCTGGGGA[C/T]GTCACAAATGAGCTC | 284434 |
rs748045584 | in-del | -/TCCA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754310 | CCATCATGTCTATCT[-/TCCA]TCCATCCATCCATCC | 284434 |
rs748048706 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16811346 | CCTAGCACTTTGGGA[A/G]GCTGAGGCGGGTGGA | 284434 |
rs748059825 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16796135 | TATTGGAAAACGTAA[C/T]ATTCAATTGGTTAAA | 284434 |
rs748084052 | in-del | -/A | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815341 | TAAAAAAATAAAAAT[-/A]AAAAAAACCCTGTGG | 284434 |
rs748102258 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16809367 | GTTTGAGCCACTGCA[C/T]CTGGCCAAGAAGTAA | 284434 |
rs748138106 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16761010 | CTGTCCCCATCAGCC[A/G]TCACTCCTCATTCCC | 284434 |
rs748139032 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16753350 | ATATCTGGTCCAATT[A/G]GTAAAGCCAGATCTC | 284434 |
rs748139726 | in-del | -/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16755196 | ATCTATATCGATCCT[-/G]TCTATCATTAATATC | 284434 |
rs748146542 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16766887 | CACTGTGCCTGACCC[C/T]CATCTTAACCATTTT | 284434 |
rs748147258 | snp | A/G | 1.64751e-05 | 0.00287007 | synonymous-codon, missense | NWD1 | GRCh38.p7 | 19:16797823 | TGAAGACATGGTGGA[A/G]ACGGCTGTTTTTGGT | 284434 |
rs748159853 | snp | A/G | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16747737 | CATCTCCCCTCTCCC[A/G]GCGCAGGCAACCATC | 284434 |
rs748224720 | snp | C/G | 3.29674e-05 | 0.00405988 | synonymous-codon, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800044 | TGCTCATAGGTCCCG[C/G]GTGCCTGCACCATTT | 284434 |
rs748266190 | in-del | -/AGA | 1.82327e-05 | 0.00301927 | intron-variant | NWD1 | GRCh38.p7 | 19:16799847 | ACTATAGTTGTCCAC[-/AGA]AGATGTCAGATCTGC | 284434 |
rs748275987 | snp | A/G | 4.96471e-05 | 0.00498208 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16791370 | TGCTTGGAATCTGGA[A/G]ACTGCAGAGCCGGTA | 284434 |
rs748276341 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16759882 | GCCTGTAATCCCAGC[C/T]GCTCGGGAGGCTGAG | 284434 |
rs748292481 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790848 | TTCACTTGTTTCTTT[A/G]TACCTTTTGTAAGGT | 284434 |
rs748322848 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16803155 | AGATCTCATGAGACT[C/T]ATTCGCTACCACAAG | 284434 |
rs748323464 | snp | A/G | 1.66446e-05 | 0.00288479 | missense | NWD1 | GRCh38.p7 | 19:16750101 | GTGCTCCTGGACCCG[A/G]AGGCCTACTGGGAGG | 284434 |
rs748362483 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16719865 | TGCTGGGAGAATTGG[G/T]CAAGGAGAGACCCAT | 284434 |
rs748378703 | snp | A/G | 1.65529e-05 | 0.00287683 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749342 | AGTCACATCACTGAC[A/G]TGCACCCAGGGGTCC | 284434 |
rs748414583 | snp | C/T | 1.64762e-05 | 0.00287016 | missense | NWD1 | GRCh38.p7 | 19:16791465 | CACTGCTGACAGTGT[C/T]CAGGGATGGTGTGGT | 284434 |
rs748466812 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16755357 | TGAGTAGCTGAGACT[A/G]CAGGTGCATGCCACC | 284434 |
rs748471944 | in-del | -/TCTT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16778493 | TCTTCTTCTTCTTCT[-/TCTT]TTTTTTTTTTTTGTT | 284434 |
rs748473946 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16726358 | CAAGAGATCCTCCTG[A/C]CCTGGCCTCTGGAAT | 284434 |
rs748515537 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16798741 | AAGCAATTCTCCTGC[C/T]TCAGCCTCGCAAGTA | 284434 |
rs748524020 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16766423 | AACAAACCAAAAAAA[A/C]ACTTATTTCTAGCTC | 284434 |
rs748554817 | snp | A/C/G/T | 0.0001236 | 0.00786052 | missense, synonymous-codon | NWD1 | GRCh38.p7 | 19:16773310 | CCGGGCAACTCTCAG[A/C/G/T]GGCTGTCACAAAGGT | 284434 |
rs748568440 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16811782 | ATCCCCCTGTGGGGC[A/G]CTTCAAAGCCTGGTT | 284434 |
rs748638152 | snp | C/T | 1.64974e-05 | 0.00287201 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16808091 | TGCCCTGCTGTGTCT[C/T]TGGGACCTGCAGGCA | 284434 |
rs748638935 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754578 | TTCTCTCTAAAGTCC[A/G]TCTATCCTTCCATCC | 284434 |
rs748669628 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16779762 | CTGCCTCAGCCTCCT[G/T]AGTAGCTGGGACTAC | 284434 |
rs748679433 | snp | A/G | 3.30551e-05 | 0.00406528 | missense | NWD1 | GRCh38.p7 | 19:16762074 | TCTCAGGGACCTGGA[A/G]CCAGGGTACCAAGAA | 284434 |
rs748704492 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16734112 | CAAATGAACTGCAAG[C/T]GTGCGGTTGCCAAGG | 284434 |
rs748732405 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16747525 | GGGACCGCAGTCACA[C/T]GCCATCACAGGTGGC | 284434 |
rs748753039 | snp | A/G | 3.29772e-05 | 0.00406048 | missense | NWD1 | GRCh38.p7 | 19:16759256 | GCGGAGCTGAAGGAT[A/G]TTTTGTCCCTGGACG | 284434 |
rs748757446 | snp | A/C/T | 0.000104086 | 0.00721341 | synonymous-codon, missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749753 | ACAGTGACCGTCCTG[A/C/T]GGCTGCTGGGGACGT | 284434 |
rs748811217 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787180 | TGCTGAGGCTGGAGT[A/G]CAGAGGAGTGATCAT | 284434 |
rs748846098 | snp | C/T | 1.64787e-05 | 0.00287038 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16779353 | TGCAGGCATCACCGC[C/T]ATGGCATGGGGTGTG | 284434 |
rs748882362 | snp | C/T | 0.000161251 | 0.00897773 | synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744583 | CCTCCCACCTACGTC[C/T]TGCAGGCACCAGGTA | 284434 |
rs748922046 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16803325 | TCCTTCATAGCAACA[A/C]CAACAGACTTAGACA | 284434 |
rs748949210 | snp | A/G | 3.29506e-05 | 0.00405884 | intron-variant | NWD1 | GRCh38.p7 | 19:16812855 | TGTGCTGGATGGTGA[A/G]TCATTTTGCTTTTAG | 284434 |
rs748951744 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16799822 | CCAATGGGCTGAAGC[A/G]TATTTCTGAACTATA | 284434 |
rs748952065 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16727225 | CTATGGTGACTACTG[C/T]GCTCTGAGGACGAGG | 284434 |
rs748970752 | snp | A/T | 1.64827e-05 | 0.00287073 | missense | NWD1 | GRCh38.p7 | 19:16779439 | TGGAAGAGCAGCATG[A/T]GATCCACATGCTAAC | 284434 |
rs748978317 | snp | C/T | 1.66217e-05 | 0.0028828 | intron-variant | NWD1 | GRCh38.p7 | 19:16791341 | GCTTCCTCTTCATTA[C/T]TCTATTAGATCAATG | 284434 |
rs748981972 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16756405 | GGACTTGGTCTTGCT[A/G]TCTCAGAGACAGCAC | 284434 |
rs749002654 | snp | A/G | 1.68573e-05 | 0.00290316 | utr-variant-3-prime, missense | NWD1 | GRCh38.p7 | 19:16815285 | AGTGCCCAGGGAAAT[A/G]AAACCAAATCAAACA | 284434 |
rs749046207 | in-del | -/TATT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16756532 | TATCTATCATCTGTC[-/TATT]TATCTTTATGTTTAT | 284434 |
rs749047949 | in-del | -/ATC | | | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16717911 | GAGTGCAGTGAGGCA[-/ATC]ATCATATCTCACTGC | 284434 |
rs749054403 | snp | G/T | 1.64917e-05 | 0.00287151 | missense, upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749256 | TTGAAGACTGCGCCC[G/T]TAGGATGGTGGACCG | 284434 |
rs749083783 | in-del | -/ATAATC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787901 | ATAATAATAATAATA[-/ATAATC]ATAATCATCATCATC | 284434 |
rs749085477 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16723855 | CGTGCACCGTCATGC[C/G]CGGCTAATTTTTGTA | 284434 |
rs749115704 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16795306 | ACTGACACAGGGCCA[A/G]GCTCCATGCAGGGCC | 284434 |
rs749123056 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790953 | ATAAAATGCATAGGC[C/T]GGGTGCAGTGGCTCA | 284434 |
rs749173668 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16766106 | TTATGTAGGTACATA[C/T]ATGATAAGAGAGAAA | 284434 |
rs749210683 | in-del | -/GGTTGAGGTTGG | 1.65302e-05 | 0.00287486 | cds-indel | NWD1 | GRCh38.p7 | 19:16765123 | CCCCTCACCTGGACT[-/GGTTGAGGTTGG]CCCCTGAGGTTGGCC | 284434 |
rs749234086 | in-del | -/G | 1.65971e-05 | 0.00288067 | frameshift-variant | NWD1 | GRCh38.p7 | 19:16797745 | AGGCTTTGGAAGATC[-/G]GTGCGGATATTCTTG | 284434 |
rs749245087 | snp | C/T | 3.4443e-05 | 0.00414973 | intron-variant | NWD1 | GRCh38.p7 | 19:16797687 | GGAATGACCCTCAAT[C/T]TCCTCTGGACATGAG | 284434 |
rs749249652 | snp | C/T | 0.000164935 | 0.00907966 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807797 | GGACCGCCTGGCCAT[C/T]GCCTATGACAACATC | 284434 |
rs749256547 | snp | C/T | 1.6519e-05 | 0.00287388 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16761988 | CTGTAGACAGCTGGT[C/T]GAGGTGGTCCGTGAG | 284434 |
rs749258094 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16735658 | ATATGGTGAAACCTT[A/G]TCTCTACTAAAAATA | 284434 |
rs749286276 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16762929 | CCTGGGACTACAGGT[G/T]TGTGCCACTGCACCT | 284434 |
rs749286836 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16771736 | TCACCAGAGGGCGCT[C/G]CTGGACAACCATGTG | 284434 |
rs749301246 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16803091 | TCACGTCTTACATGG[C/T]GGCAGGCAAGAGAGT | 284434 |
rs749337340 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16758659 | TGCATTATTTTCCTT[C/G]AGTTACCACTTCCCT | 284434 |
rs749340145 | in-del | -/C | 3.35289e-05 | 0.0040943 | frameshift-variant | NWD1 | GRCh38.p7 | 19:16750015 | GCTGCCTCTCAACTG[-/C]CCCCCCGAGGGTGCA | 284434 |
rs749372142 | snp | G/T | 1.6489e-05 | 0.00287128 | missense | NWD1 | GRCh38.p7 | 19:16808081 | GGTCTGAGGATGCCC[G/T]GCTGTGTCTCTGGGA | 284434 |
rs749398259 | snp | C/T | 8.40131e-05 | 0.0064807 | missense | NWD1 | GRCh38.p7 | 19:16749985 | ACTCTGTCCGCCATG[C/T]TCGGAGGGTTCCCTG | 284434 |
rs749399264 | in-del | -/CTTCCCC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16770315 | TTTTAAAATAAGGGG[-/CTTCCCC]CTTCCCCCTTTGCTC | 284434 |
rs749399712 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16770725 | TTCACACAGAACCTC[C/T]ACCCGTGTTGCCATC | 284434 |
rs749402886 | snp | C/T | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816249 | CAAACAAGCCCACTG[C/T]TGTCAGTGCTTCCAG | 284434 |
rs749430523 | snp | C/G | 1.65844e-05 | 0.00287957 | missense, utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16799952 | GGGGCCCCCGTGAGC[C/G]TGCTGGCCCGCGGCG | 284434 |
rs749479017 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16730125 | TCAGGAGATTGAAAC[C/G]ATCCTGGCCAACATG | 284434 |
rs749503123 | snp | C/T | 5.0363e-05 | 0.00501787 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749182 | GCTGAGCTCAGAGGA[C/T]CGGGAACAGGGAGCC | 284434 |
rs749508047 | snp | A/G | 0.000133576 | 0.0081713 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750052 | CCTCTCAGCTTGCTC[A/G]GGGGCACTGGGGGTT | 284434 |
rs749589901 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16783878 | TTACATAGCACGTAT[A/G]CCATATTAGGTATTG | 284434 |
rs749603191 | snp | C/T | 1.6894e-05 | 0.00290633 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750283 | AGCCCGGAAATGGGC[C/T]TCTTTCACCGTGCCT | 284434 |
rs749619319 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16739733 | AGTCATTAGGCAGCA[A/C]CGAGGCCGGGGACAG | 284434 |
rs749636336 | snp | C/T | 1.66252e-05 | 0.00288311 | missense | NWD1 | GRCh38.p7 | 19:16791621 | ATGGCTCCATCTCTT[C/T]GGTAAGCACCTTTAC | 284434 |
rs749650303 | snp | A/G | 1.74756e-05 | 0.00295593 | missense | NWD1 | GRCh38.p7 | 19:16807663 | CGCAAGCTCCTATTT[A/G]CGGGCCTCGTGTCGG | 284434 |
rs749662023 | in-del | -/AAAC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16762559 | CTCTGTCTCAAAAAC[-/AAAC]AAACAAACAAACAAA | 284434 |
rs749662550 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16810374 | ACCTGGAAGGCAGAG[G/T]CTGCAGTGAGCCGAG | 284434 |
rs749663333 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16770890 | ATGTGAAGATGCTGG[-/T]GCCTGCAATCATTTA | 284434 |
rs749670568 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16792018 | CGTGCCCGGCCACAC[A/G]CTTGGCTTCTTAATC | 284434 |
rs749701483 | snp | A/C | 0.000115705 | 0.00760521 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16773128 | CCCTTTGTTGCAGAG[A/C]GGAGCCTCCTGTACA | 284434 |
rs749757739 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16753665 | CTGAGTGGAGTCCAG[A/G]GATGCTGTTTAACAC | 284434 |
rs749762437 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16719803 | CTGGGCTGAATGCCC[A/G]GCTAAGCTGGTGCCC | 284434 |
rs749857588 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16759785 | GATCACCTGAGGTCA[A/G]GAGTTTGAGACCAGT | 284434 |
rs749865035 | snp | C/G | 1.64762e-05 | 0.00287016 | missense | NWD1 | GRCh38.p7 | 19:16791434 | ATGTGCATGGCCGTG[C/G]TGGCCTCCCAGGCCA | 284434 |
rs749879651 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16814146 | GCCTGGGCAACAGAG[C/T]GAGACCCTGTCAAAA | 284434 |
rs749974742 | snp | G/T | 1.65674e-05 | 0.00287809 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749378 | ACCCACCGCCTGCCG[G/T]GGAGCCGCGACTTGG | 284434 |
rs749984963 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16812519 | ACTCAAAATACAAAA[A/C]TTAGCCAGGCATGGT | 284434 |
rs749993476 | snp | A/G | 1.65542e-05 | 0.00287695 | missense | NWD1 | GRCh38.p7 | 19:16765136 | ACTCCCCTGAGGTTG[A/G]CCTGGTCCGTGAAGC | 284434 |
rs749995237 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16727171 | AAGAGGTTGGCTGGT[C/T]CCCGGGCCCCAATGC | 284434 |
rs750000811 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16743511 | CCATGCCTAGCCTAG[C/G]GGACAATTCTTTATT | 284434 |
rs750028410 | in-del | -/C | 3.29565e-05 | 0.00405921 | frameshift-variant | NWD1 | GRCh38.p7 | 19:16791423 | TGATCCTTGGATGTG[-/C]CATGGCCGTGCTGGC | 284434 |
rs750039473 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16813621 | AGCTGGGATTACGGG[C/T]GCCCACCACCACACT | 284434 |
rs750042903 | snp | A/G | 3.55461e-05 | 0.00421566 | intron-variant | NWD1 | GRCh38.p7 | 19:16765215 | CAGATGGCCTGGATA[A/G]GAGTGACCAGGACGG | 284434 |
rs750059393 | snp | A/G | 1.64882e-05 | 0.00287121 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16759243 | CGGTCTCTCGGAGGC[A/G]GAGCTGAAGGATGTT | 284434 |
rs750062320 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16781468 | AAAAAATGCAAAAAT[A/T]AGCCAGGCATGGTGG | 284434 |
rs750086770 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16746814 | ACAAGGAAGAGAAAA[C/T]ATGTTTGCTGTTGAT | 284434 |
rs750116922 | in-del | -/A | 1.68289e-05 | 0.00290072 | intron-variant | NWD1 | GRCh38.p7 | 19:16808173 | GTTCATGCTAGACCC[-/A]GGCATTGGAAAACTG | 284434 |
rs750135719 | snp | A/G | 0.000131843 | 0.00811815 | missense | NWD1 | GRCh38.p7 | 19:16807840 | GACATCACCTCCGGG[A/G]ACCCCTGCCCGGTCA | 284434 |
rs750189428 | snp | C/G | 2.06337e-05 | 0.00321192 | intron-variant | NWD1 | GRCh38.p7 | 19:16773350 | CAGCATAGCAAAAAT[C/G]CCAGCAGGCACCTGC | 284434 |
rs750191697 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16775427 | GACCCATACTCTTTC[A/T]GTCTGGCGCTCTGCC | 284434 |
rs750224003 | snp | C/T | 3.32723e-05 | 0.00407861 | intron-variant | NWD1 | GRCh38.p7 | 19:16808142 | GAGCTACACGGTGGG[C/T]GGCCCGCCTCCCCAT | 284434 |
rs750228780 | snp | C/T | 4.94173e-05 | 0.00497053 | intron-variant, missense | NWD1 | GRCh38.p7 | 19:16812782 | AATGTGCTTGCTTCT[C/T]CAAGGATGACAAGTA | 284434 |
rs750250361 | snp | C/G | 1.67133e-05 | 0.00289074 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750040 | GGTGCACCTCATCCT[C/G]TCAGCTTGCTCGGGG | 284434 |
rs750256153 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16788895 | CTTTGGTAAATGAGG[A/G]TATTTCCAAGCTGAC | 284434 |
rs750269027 | snp | C/T | 1.64838e-05 | 0.00287083 | synonymous-codon, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800026 | GGTCTGGGATCTCAG[C/T]GATGCTCATAGGTCC | 284434 |
rs750271601 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16793696 | ATTCTCCTGCCTCCG[C/T]CTCCCCAGTAGCTGG | 284434 |
rs750282765 | in-del | -/GAAG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16729909 | AAAGAGAGAGAGAAG[-/GAAG]GAAGGAAGGAAGGAA | 284434 |
rs750347429 | snp | A/G | 4.94792e-05 | 0.00497365 | missense, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800072 | TTTCTGGACCGCACC[A/G]GCCTCACCGCAGTGT | 284434 |
rs750357687 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16727917 | AATACAAAAAATTAG[C/T]TGGGCGTAGTGGTGG | 284434 |
rs750357938 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16735242 | GGTGCAGTAGCTCGT[G/T]CCTGTAATCCTAACA | 284434 |
rs750371778 | snp | A/G | 1.67756e-05 | 0.00289612 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749282 | GACCGGCTCGCGGAT[A/G]GCTGCCTGGACGCTG | 284434 |
rs750373298 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16758151 | TGGAACACTTGAAAG[A/G]TGCTTCACACAACTC | 284434 |
rs750375059 | snp | A/T | 1.66479e-05 | 0.00288508 | missense | NWD1 | GRCh38.p7 | 19:16750087 | ACACCTTGCAGCGGG[A/T]GCTCCTGGACCCGGA | 284434 |
rs750425937 | in-del | -/T/TT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16730911 | ATTTTTCTTTCTTTC[-/T/TT]TTTTTTTTTTTTTTT | 284434 |
rs750454565 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16800810 | CACTCTGCTACAGTT[C/T]GGAGGTTTGGCCCTA | 284434 |
rs750470383 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16796744 | TCTCCTTCCTCCCTT[C/G]CTTCCATCATAGTTA | 284434 |
rs750477435 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16795986 | TTGAAAAGTGATAAG[A/G]ACAGAGAATTTTATT | 284434 |
rs750480534 | snp | A/G | 5.13809e-05 | 0.00506831 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750331 | CGCAGAGGAAGCCAC[A/G]CACCAACTCTGCACC | 284434 |
rs750504231 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16804163 | AAGGGTTGAGCAAGA[A/G]TGCAGGCTCAGCTAA | 284434 |
rs750510819 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16809847 | CAGTCATGAGCCACC[A/G]TGCCTGGCTGCTCCG | 284434 |
rs750540750 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16720620 | GAGTGCAGTGGCGTG[A/G]TCTCAGTTACTGCAA | 284434 |
rs750588008 | snp | C/T | 0.000428093 | 0.0146241 | missense | NWD1 | GRCh38.p7 | 19:16773290 | CAGCCCCCGGGAGGA[C/T]CCCTCCGGGCAACTC | 284434 |
rs750602579 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764027 | CCTGGGGAGGGTGAA[C/G]GGCAAACATGGAAAT | 284434 |
rs750657013 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16723722 | TGTTTTGTTTTGAGA[C/T]GGACTGTCCCTCTGT | 284434 |
rs750682081 | snp | C/T | 0.000131865 | 0.00811882 | splice-donor-variant | NWD1 | GRCh38.p7 | 19:16736752 | GGCCAGCTTTTGTTG[C/T]GAGTGTCTTGGGAGG | 284434 |
rs750685087 | snp | A/G | 1.81658e-05 | 0.00301373 | intron-variant | NWD1 | GRCh38.p7 | 19:16799858 | CCACAGAAGATGTCA[A/G]ATCTGCCCTCCTGTT | 284434 |
rs750702971 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16763373 | ATATTCAGTGCCTTC[A/G]TGATCTGCTGCTTAC | 284434 |
rs750704377 | in-del | -/AC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16811053 | TAATTTTTTGTAGAG[-/AC]AGGGTTTCACCCACC | 284434 |
rs750705263 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16765343 | GCAGTGCTTCTAGAA[-/T]TTTTTTTTGACATGT | 284434 |
rs750706465 | snp | A/G | 0.000167836 | 0.00915914 | intron-variant | NWD1 | GRCh38.p7 | 19:16808167 | CCCCATGTTCATGCT[A/G]GACCCAGGCATTGGA | 284434 |
rs750746935 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16759697 | GCCTGGGCAACGTAG[C/T]GAGGCCCCATCTCTA | 284434 |
rs750749214 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16772850 | AAGGAAGAAAGGAAG[A/G]GAGAGAGGGAGAGAA | 284434 |
rs750762939 | snp | A/C | 3.55486e-05 | 0.00421581 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749130 | TTCCCACCTTCCCCA[A/C]TTTGGCAGTCATTGA | 284434 |
rs750864122 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787959 | ATAGGCCAGGCGCGG[C/T]GGCTCATGCCTGTAA | 284434 |
rs750875351 | snp | A/T | 1.68935e-05 | 0.00290628 | missense | NWD1 | GRCh38.p7 | 19:16750278 | GAGGAAGCCCGGAAA[A/T]GGGCCTCTTTCACCG | 284434 |
rs750924778 | snp | C/T | 1.66801e-05 | 0.00288787 | intron-variant | NWD1 | GRCh38.p7 | 19:16763958 | TGGGTAAGGGCTGCC[C/T]CCCATCTCAGAGGAC | 284434 |
rs750953815 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754701 | TCCATCCATCATCTC[C/T]AGCATCCATCCATCC | 284434 |
rs750989988 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16785686 | TGTATATATTTATGC[C/T]TTATGTATGTAAAAC | 284434 |
rs750993806 | snp | A/G | 8.3736e-05 | 0.00647001 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750022 | TCTCAACTGCCCCCC[A/G]AGGGTGCACCTCATC | 284434 |
rs751007669 | in-del | -/C | 1.6601e-05 | 0.00288101 | frameshift-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749467 | GGTGAGGGCCAATCA[-/C]CAGGTCCTCACACGC | 284434 |
rs751016845 | snp | C/T | 1.65002e-05 | 0.00287225 | missense, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16799986 | CTTTGGTGGCATCTG[C/T]TTCCCCACAGTCCTC | 284434 |
rs751026608 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16780463 | GCCCAGCCAAAGGCA[C/G]GGTTTCAAGAAAACA | 284434 |
rs751132985 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16740760 | TACAGGTGTGAGCCA[C/T]CGCACTGGCCCAGGT | 284434 |
rs751161561 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16721051 | GATGGGGTTTCGCCA[C/T]GTTGGCCAGGCTGGT | 284434 |
rs751190666 | snp | C/G | | | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749170 | AGAGCGGAGCCTGCT[C/G]AGCTCAGAGGACCGG | 284434 |
rs751200738 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16720432 | ACAACATGAACAGAT[A/G]CAGCATAGAGCACTA | 284434 |
rs751217041 | in-del | -/AGGGACCTGGAGGGACCTGG | 1.65605e-05 | 0.0028775 | frameshift-variant | NWD1 | GRCh38.p7 | 19:16762093 | GGTACCAAGAAGCTC[-/AGGGACCTGGAGGGACCTGG]ATCACTCTGCCACTT | 284434 |
rs751260273 | snp | G/T | 1.7345e-05 | 0.00294486 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815358 | AAAAAACCCTGTGGG[G/T]GTATGGGGCTCCAGT | 284434 |
rs751283494 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16791802 | CACTGCAACCTCCGC[C/T]TCTCGGGTTCAAGCG | 284434 |
rs751296376 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16805442 | CAAGCAATCTGCCTG[C/T]CTCAGCCTCCCAAAG | 284434 |
rs751334113 | snp | A/C | 1.65326e-05 | 0.00287507 | missense | NWD1 | GRCh38.p7 | 19:16773185 | TTCGCCACCTCACAT[A/C]CAGCACTGGTGGGAC | 284434 |
rs751374504 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751173 | AGGTTGCCGTGAGCC[A/G]AGATCACGCCATTGC | 284434 |
rs751392104 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16772183 | CCAGCCTGGGCAACA[G/T]AACGAGACCCCGTCT | 284434 |
rs751401180 | in-del | -/AG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16778941 | TGGGATGGGGTTGTC[-/AG]ATGCGTTGCTGGGTG | 284434 |
rs751421197 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16808040 | CTGTGTGGAGGTCAG[C/T]CACAAGGAGCAGCTG | 284434 |
rs751446071 | snp | A/C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16756088 | AAAGAAAATGATAGT[A/C/G]AGAAAATCATAAAGG | 284434 |
rs751456769 | snp | A/G | 8.48486e-05 | 0.00651284 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16773283 | ATTCCTCCAGCCCCC[A/G]GGAGGACCCCTCCGG | 284434 |
rs751458673 | snp | A/G | 1.67649e-05 | 0.0028952 | intron-variant | NWD1 | GRCh38.p7 | 19:16761957 | TCACCCAGGTCTATC[A/G]GTCTGTATACCCTCT | 284434 |
rs751481943 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16726911 | CCAGACATTGCAAGT[A/G]TCCCCTGGGGGCTGA | 284434 |
rs751486901 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16742052 | CCACTGCACGCCAGC[C/T]TGGGTGACAGAGTGA | 284434 |
rs751532845 | snp | A/G | 0.00020084 | 0.010019 | missense, utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16799934 | GACATCCTGGAAGGC[A/G]TCGGGGCCCCCGTGA | 284434 |
rs751555185 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16796906 | ATTACTGGCTGGGTA[C/T]GGTGGCTCAGGCCTG | 284434 |
rs751600150 | in-del | -/AAAAGAAAAT/AAAAT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16738010 | AAAAGAAAAGAAAAG[-/AAAAGAAAAT/AAAAT]AAATTCTAGAGCAGA | 284434 |
rs751621465 | snp | C/T | 3.295e-05 | 0.00405881 | utr-variant-3-prime, missense | NWD1 | GRCh38.p7 | 19:16815102 | AGTGGCTTCATTGCC[C/T]CCACCAGGCATGGTT | 284434 |
rs751633850 | snp | A/C | 1.64741e-05 | 0.00286998 | missense | NWD1 | GRCh38.p7 | 19:16807926 | GGCCATTCTGACGGA[A/C]TACCGCGTGGTCTAC | 284434 |
rs751634485 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16722855 | GTGGTCAATCATGTC[C/T]ACGTGACCAACTCCC | 284434 |
rs751634711 | snp | A/G | 1.64852e-05 | 0.00287094 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807635 | GATCAGGTGTCTGGA[A/G]GTTGCTGAGCAGCGC | 284434 |
rs751691371 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16752529 | TGAGCATGGTGGTGC[A/T]ACTCCGGAGGCTGAG | 284434 |
rs751735339 | in-del | -/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16810458 | AAAAAAAAAAAAAAA[-/G]AAAGAAAAAGAAGGC | 284434 |
rs751748187 | in-del | -/C | | | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718169 | CAGCACCTGAAACTT[-/C]TTTTTTTTTTTTTTT | 284434 |
rs751748465 | in-del | -/C | 3.30699e-05 | 0.00406618 | frameshift-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749301 | GCCTGGACGCTGATG[-/C]CCAGAACCTTCTCAG | 284434 |
rs751766162 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16762222 | CTTCCCCTTTTTGCA[C/T]TCGAAATGTCCTCCC | 284434 |
rs751768291 | snp | C/T | 1.66004e-05 | 0.00288096 | synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749482 | CCAGGTCCTCACACG[C/T]CTCCGTGAGCTGGAT | 284434 |
rs751817266 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16774726 | CCCATCCATTCATCC[A/T]TTCATTCATCCTTCA | 284434 |
rs751827657 | in-del | -/T/TTTTATTTTC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16760275 | TTTTATTTTATTTTA[-/T/TTTTATTTTC]TGTATTTTGAGACAG | 284434 |
rs751838537 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16735859 | AGGAAGGAAGGAAGG[-/A]AGGAAGGAGGAAGGA | 284434 |
rs751859293 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16746922 | TCTTGCTGTCTCAGG[A/G]GTGGCAGAGGCAGAA | 284434 |
rs751886416 | snp | A/G/T | 6.92489e-05 | 0.00588391 | synonymous-codon, missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749818 | GAGCATCTGCTTCCA[A/G/T]GTGTGCCTGGCCTAT | 284434 |
rs751890862 | snp | C/T | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815838 | GACCACAGAACCTCA[C/T]AGTTTATAAAGCTGT | 284434 |
rs751928945 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16784423 | GGAGGATATATATAG[A/G]CTATATGCAAATACG | 284434 |
rs751942327 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16814637 | GTAGCAAAGATATAT[A/G]CAACTGGTATAAAGT | 284434 |
rs751986842 | snp | C/G | 1.6651e-05 | 0.00288535 | intron-variant | NWD1 | GRCh38.p7 | 19:16763779 | GCTTGTGCGTGGAGT[C/G]AATGAATGGGTTTGT | 284434 |
rs752026663 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16753814 | ATCCCTCCCTCCCTC[A/C]CTCCATCATCTCTAT | 284434 |
rs752035008 | snp | C/G | 1.6507e-05 | 0.00287284 | missense, utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16797864 | ACCTGATCATCACGG[C/G]GTCCCTTGATGCGCT | 284434 |
rs752088956 | snp | A/G | 1.65974e-05 | 0.0028807 | synonymous-codon, utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16797886 | TGATGCGCTCATTCA[A/G]GTGAGGGGAGATCTG | 284434 |
rs752100312 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16763120 | TTCTCTTCTCCCCCC[A/G]AGACCCATTCACAAA | 284434 |
rs752111178 | snp | G/T | 3.36717e-05 | 0.00410302 | intron-variant | NWD1 | GRCh38.p7 | 19:16761950 | TGATGGGTCACCCAG[G/T]TCTATCAGTCTGTAT | 284434 |
rs752112623 | snp | C/T | 0.000163894 | 0.00905098 | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744766 | ACAAGAAACTGACCA[C/T]GTGTTCAGAATATCC | 284434 |
rs752164086 | snp | A/G | 3.63379e-05 | 0.00426235 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749104 | GCTGACCCAATAATG[A/G]CCACACTTCCTTCCC | 284434 |
rs752180002 | in-del | -/AAATAAATAAATA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790643 | ACATTAAAAAAAAAT[-/AAATAAATAAATA]AATAAATAAATAAAT | 284434 |
rs752181564 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16739329 | GACCCTATCTCTACC[-/A]AAAAAAAAAAAAAAA | 284434 |
rs752190172 | snp | A/G | 3.29533e-05 | 0.00405901 | missense | NWD1 | GRCh38.p7 | 19:16808018 | AGACCCACAGGAGCC[A/G]AGTTGCCTGTGTGGA | 284434 |
rs752205972 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16778175 | TACACATGTGGAAGA[A/G]GCACACAGAAGGAAA | 284434 |
rs752206202 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16803562 | ATTTTAACATAGGAA[C/T]TTGTCAGGGGGACAC | 284434 |
rs752206353 | snp | A/C | 1.68915e-05 | 0.00290611 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749934 | GCAGAAACTTCGAGT[A/C]TCTCGTGCTCCTGCT | 284434 |
rs752253737 | in-del | -/CCTCC | 1.66012e-05 | 0.00288103 | frameshift-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749482 | CCAGGTCCTCACACG[-/CCTCC]GTGAGCTGGATACGG | 284434 |
rs752259004 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790376 | ATAAGTAATTGGTGG[C/T]TGTTGACAGTAATAT | 284434 |
rs752293658 | snp | C/T | 1.79897e-05 | 0.00299908 | intron-variant | NWD1 | GRCh38.p7 | 19:16799875 | TCTGCCCTCCTGTTC[C/T]GCTTCCTCAGGTGTG | 284434 |
rs752327746 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16730771 | TGGTGGCTCATGTCT[A/G]TAATCCCAACACTTT | 284434 |
rs752331132 | snp | A/G | 1.67562e-05 | 0.00289444 | missense | NWD1 | GRCh38.p7 | 19:16750012 | CCTGGCTGCCTCTCA[A/G]CTGCCCCCCGAGGGT | 284434 |
rs752332980 | snp | A/G | 1.74418e-05 | 0.00295307 | stop-gained, upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749148 | TGGCAGTCATTGAGT[A/G]GGAGATAGAGCGGAG | 284434 |
rs752339892 | snp | C/T | | | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16719256 | TTCTTGTGCCTCAGC[C/T]TCCCAAGTAGCTGGG | 284434 |
rs752386089 | snp | G/T | 3.3012e-05 | 0.00406262 | missense, upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749215 | CGTCTTCCTTAGAGA[G/T]ATCCAAGACCTCCAC | 284434 |
rs752387877 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16759536 | TCACTTACCATTCCC[A/G]GGGAATCAAGTCCAG | 284434 |
rs752392209 | in-del | -/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16752213 | CTCTTCTCAGTTTTA[-/G]GGTTGTTTTTTTTTT | 284434 |
rs752393605 | snp | A/G | 6.62789e-05 | 0.00575631 | synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749395 | GAGCCGCGACTTGGT[A/G]AACCCCAAGAACAAG | 284434 |
rs752440689 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16771373 | GAAAATTGCTTGAAC[C/G]CGGGAGGCAGATGTT | 284434 |
rs752474837 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754983 | TCAATCTATCTCTAT[C/T]ACTTCTAGTAATCTA | 284434 |
rs752483053 | snp | A/G | 1.65482e-05 | 0.00287643 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16791580 | CTCAGTCCAGAAGCA[A/G]GGAAAGCTTGTTACC | 284434 |
rs752496128 | snp | C/T | 1.68667e-05 | 0.00290397 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750248 | GGGAACCCAGGGCGG[C/T]TGAGGCTGGCGTTTG | 284434 |
rs752517971 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16810034 | TGAGCTCTGTCTGGG[A/C]AAAAGGATTTTTTTG | 284434 |
rs752545076 | snp | G/T | | | missense | NWD1 | GRCh38.p7 | 19:16750207 | CGGTGCACACAGATT[G/T]GCTCTGGGCCAGCCT | 284434 |
rs752549089 | snp | C/T | 1.65938e-05 | 0.00288039 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749465 | GTGGTGAGGGCCAAT[C/T]ACCAGGTCCTCACAC | 284434 |
rs752565165 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16724611 | TCAGCACTTTGGGAG[A/G]CTCAGGTGGGAGGAT | 284434 |
rs752567832 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16811128 | CACATCCAGCCTTTA[C/T]TGGAATCTTACCAGC | 284434 |
rs752620481 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16779134 | CCCTTCCCTACCTAA[A/G]AGCGAAGTGAATGTC | 284434 |
rs752635761 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16739243 | CATGCCTGTAATCCC[A/G]CACTTCAGGAGGCTG | 284434 |
rs752661454 | snp | A/G | 3.99752e-05 | 0.00447057 | missense | NWD1 | GRCh38.p7 | 19:16759353 | CCCTGCTGTGGGTGC[A/G]GCTTCGTCGGGATCT | 284434 |
rs752662123 | snp | G/T | 1.64732e-05 | 0.0028699 | missense | NWD1 | GRCh38.p7 | 19:16807936 | ACGGACTACCGCGTG[G/T]TCTACAGCATGACCA | 284434 |
rs752667845 | in-del | -/ATTTT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16760240 | TCACCATTTTATTTT[-/ATTTT]ATTTTATTTTATTTT | 284434 |
rs752675198 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16738447 | GGTGGCACATGCCTG[C/T]GATCCCAGCTACTTG | 284434 |
rs752708944 | snp | A/G | 1.64787e-05 | 0.00287038 | stop-gained | NWD1 | GRCh38.p7 | 19:16779419 | CATCATGGCTGTGTG[A/G]GACATGGAAGAGCAG | 284434 |
rs752721073 | in-del | -/GC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16738630 | TTTCTGAGATCTATT[-/GC]TTCTGAGACCTAAAG | 284434 |
rs752737821 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16774528 | ACTGTTTCATTTATC[C/T]AGCCCCATTCATCCA | 284434 |
rs752769430 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16733785 | TCAACATCCTCCACA[C/T]GCACATCGGGAGACG | 284434 |
rs752817167 | snp | C/T | 1.64727e-05 | 0.00286986 | intron-variant, missense | NWD1 | GRCh38.p7 | 19:16812812 | ATGTGTACGTGGGCT[C/T]AAAGGATCGCTCTAT | 284434 |
rs752834055 | snp | C/T | 3.97875e-05 | 0.00446007 | intron-variant | NWD1 | GRCh38.p7 | 19:16762185 | GCAACCTCCACCCTG[C/T]CTGGCATTGCTCACC | 284434 |
rs752839067 | snp | C/T | 1.67318e-05 | 0.00289234 | missense | NWD1 | GRCh38.p7 | 19:16750174 | TCCTGCTGGCAGCTG[C/T]AAGGAGGACGCTGAG | 284434 |
rs752846876 | snp | C/T | 0.000162509 | 0.00901267 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744712 | TGGCAGCACTACCAC[C/T]GGTCAGGTGAGGCCG | 284434 |
rs752873444 | snp | A/T | 0.000131967 | 0.00812197 | synonymous-codon, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800083 | CACCGGCCTCACCGC[A/T]GTGTCCCACAATGGA | 284434 |
rs752910920 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16769058 | AAGCCCAAAACGGCC[A/G]GGGTGGCTCAAGCCT | 284434 |
rs752916673 | snp | A/C/T | | | intron-variant, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800304 | TTTGGGAGGCCTTGG[A/C/T]GGGTGGATCACCTGA | 284434 |
rs752926820 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16799367 | CGCTTGGCTGATTTT[C/T]GTATTTTTAGTAGAG | 284434 |
rs752949337 | in-del | -/AA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16807171 | CCAGAATACTGTCTC[-/AA]AAAAAAAAAAAAAAA | 284434 |
rs752957552 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16781578 | CTGTGATTACACCAC[C/T]GTACTCTAGCCTGTG | 284434 |
rs752961025 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16784839 | GAGGCTGAGGCAAGA[A/G]AATCACTTGAACCCG | 284434 |
rs752965700 | snp | C/G | 1.65037e-05 | 0.00287256 | missense | NWD1 | GRCh38.p7 | 19:16765101 | GCTGGATGACTTTGA[C/G]CTGTGTGCCCCTCAC | 284434 |
rs752985268 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16785950 | GCTCCCTGCAACCTC[C/T]GCCTCCCAGGTTCAA | 284434 |
rs752986608 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16745326 | TACAATTCAAGATGA[A/G]ATTTGGGTGAAGACA | 284434 |
rs753001812 | snp | C/T | 1.76999e-05 | 0.00297483 | intron-variant, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800181 | GGTAAGGTATAAGTA[C/T]GGTCATTTTTGTGGG | 284434 |
rs753043575 | snp | C/T | 6.7432e-05 | 0.00580616 | intron-variant | NWD1 | GRCh38.p7 | 19:16797724 | AACCCCAGTTCCTGC[C/T]GTTTCAGGCTTTGGA | 284434 |
rs753056090 | snp | A/G | 0.000136154 | 0.00824974 | intron-variant | NWD1 | GRCh38.p7 | 19:16750415 | TGTGTCTTCCCGGTA[A/G]GTCTCTGTGTTTTGA | 284434 |
rs753061393 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16742445 | AATGTGGCGCTTTCA[C/T]ACTGAGCTCTGATCT | 284434 |
rs753114396 | snp | A/G | 3.44542e-05 | 0.00415041 | synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749656 | GCACACCCCCCTGGT[A/G]CTCTTTGGGCCCCCA | 284434 |
rs753114586 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16794718 | TCCAGACGAGACAAC[C/T]TCAGTTGCAAAGACT | 284434 |
rs753146369 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16722702 | TCTAAGCCCTTGGAA[A/T]GGGATAAGGGTGTCT | 284434 |
rs753183197 | in-del | -/TGTTT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16723681 | CAGCTTTTTCTGTTT[-/TGTTT]TGTTTTGTTTTGTTT | 284434 |
rs753198049 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782093 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAG | 284434 |
rs753210716 | in-del | -/TTTTTTG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16793558 | TTTTTTTTTAACTGT[-/TTTTTTG]TTTTTTGTTTTTTGG | 284434 |
rs753230216 | snp | A/T | 1.64857e-05 | 0.00287099 | intron-variant | NWD1 | GRCh38.p7 | 19:16779332 | TTGCTGTTGCCTCTG[A/T]GTGGCTGCAGGCATC | 284434 |
rs753236371 | snp | A/G | | | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16721474 | GACCCAGGAAAACGA[A/G]AGAAGGAACAGAAAT | 284434 |
rs753243906 | snp | A/G | 0.000113398 | 0.00752902 | intron-variant | NWD1 | GRCh38.p7 | 19:16765236 | ACCAGGACGGGCACT[A/G]ACTTCTAGAAACATG | 284434 |
rs753246029 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751379 | AGAGAGAGAGAAAGA[A/G]GGAAGAAAGGCAGAC | 284434 |
rs753279421 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16758285 | TTCATGTATTTATGT[A/G]TTTATTTTAGAGACA | 284434 |
rs753284831 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16767791 | GAGCCAACCCATATC[A/T]CTCCCCATTCTCCCT | 284434 |
rs753313970 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16793571 | TGTTTTTTTGTTTTT[C/T]GGTTTTTGGTTGTTT | 284434 |
rs753314039 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16807327 | GGAGAAACCCCACCT[A/T]TACTAAAAATACAAA | 284434 |
rs753374133 | snp | A/G | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815672 | CAATTATTATATCTG[A/G]GAGAATGCAGAGCTC | 284434 |
rs753393601 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16801038 | ATACCAGCACTTTGG[A/G]AGGCCAAGGCAGGCA | 284434 |
rs753424516 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16769225 | CCAGCACTTCGGGAG[C/G]CTGAGGCAGGCAGAT | 284434 |
rs753449568 | in-del | -/AAA/AAAA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790632 | ACTGAAAGTAACATT[-/AAA/AAAA]AAAAAAAAATAAATA | 284434 |
rs753461782 | snp | G/T | 3.38175e-05 | 0.00411189 | intron-variant | NWD1 | GRCh38.p7 | 19:16761940 | CCTTTGAGCTTGATG[G/T]GTCACCCAGGTCTAT | 284434 |
rs753480061 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16757429 | AATGAGATCATACTC[A/G]CCAGAATAAGAGTTC | 284434 |
rs753480089 | snp | C/T | 1.73174e-05 | 0.00294251 | synonymous-codon, intron-variant | NWD1 | GRCh38.p7 | 19:16749824 | CTGCTTCCAGGTGTG[C/T]CTGGCCTATGGGCTG | 284434 |
rs753520020 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16770427 | AGGCCTCCCCAGCCC[G/T]GCAGAACTGTAGGTC | 284434 |
rs753523820 | snp | A/G | 3.32917e-05 | 0.0040798 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750094 | GCAGCGGGTGCTCCT[A/G]GACCCGGAGGCCTAC | 284434 |
rs753545227 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16743565 | CCAGGCTATAAGGGC[C/G]GTCAACTTCACCTCC | 284434 |
rs753570115 | snp | G/T | 0.000331126 | 0.0128629 | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744789 | GAATATCCATCCCCT[G/T]TTGGCAAAAATGCAA | 284434 |
rs753570240 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16783022 | TCTTTCTTTCCTTCT[C/T]TCTTTCTTTTCTTTC | 284434 |
rs753586666 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16814393 | AGGCGCTCATTGTGT[A/G]TTATCTCTTTGAACC | 284434 |
rs753607240 | in-del | -/TTTA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16747350 | GACATTTTCTTTTTA[-/TTTA]TTTATTTATTTATTT | 284434 |
rs753609515 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16809882 | ATTTCTTTATCCAAC[A/T]GATACTTATTGAAAA | 284434 |
rs753631547 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16762175 | TTCCCCACCTGCAAC[C/T]TCCACCCTGCCTGGC | 284434 |
rs753648158 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16778926 | GGGCTGAATCTTTCT[C/G]TGGGATGGGGTTGTC | 284434 |
rs753665483 | in-del | -/T | 1.64749e-05 | 0.00287005 | intron-variant | NWD1 | GRCh38.p7 | 19:16812735 | AGATCATATTGTCTG[-/T]TTTCAACAGAGTTCT | 284434 |
rs753673424 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16767625 | TCTCCAATAAAACCC[-/A]AAAAACCATCAGATC | 284434 |
rs753689045 | snp | A/G | 3.30502e-05 | 0.00406497 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749291 | GCGGATGGCTGCCTG[A/G]ACGCTGATGCCCAGA | 284434 |
rs753694891 | snp | C/T | 1.65217e-05 | 0.00287412 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16791565 | ACCTACCTGTGCCGT[C/T]TCAGTCCAGAAGCAA | 284434 |
rs753730091 | in-del | AGT/GGCACCATGTCG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16741424 | AGGCTGGAGTGCAGT[AGT/GGCACCATGTCG]GTTCACTGAAACCTC | 284434 |
rs753752543 | snp | A/G | 1.75715e-05 | 0.00296402 | intron-variant, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800176 | AGGTTGGTAAGGTAT[A/G]AGTATGGTCATTTTT | 284434 |
rs753770748 | in-del | -/TTT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16778488 | TCTTTCTTCTTCTTC[-/TTT]TTCTTCTTTTTTTTT | 284434 |
rs753780597 | in-del | -/CAT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764376 | GTCCATCCATCCATC[-/CAT]CCATCCATCCATCCA | 284434 |
rs753785552 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790231 | GGGAACTCAGTGACC[C/T]TGGTTGTGTCATTCA | 284434 |
rs753796796 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16759124 | AGGTGATGTGCTGGA[C/T]ACCGCGCGGGTGGCT | 284434 |
rs753810178 | snp | A/G | 4.97063e-05 | 0.00498505 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749385 | GCCTGCCGTGGAGCC[A/G]CGACTTGGTGAACCC | 284434 |
rs753875281 | snp | A/C | 1.73884e-05 | 0.00294854 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749717 | CTGGCTGAGCAGATG[A/C]CAAGGCTGCTGGGGC | 284434 |
rs753877228 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16784505 | GGGTGAAGGAAGGGC[A/T]GGGGAGAGGAAAGAG | 284434 |
rs753905579 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16785494 | CCAGCCTGGGAGACA[C/G]AGTGAGACTCTGTCT | 284434 |
rs753911477 | snp | C/G | 1.70828e-05 | 0.00292252 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749642 | GATGACAGCAAGCAG[C/G]ACACCCCCCTGGTAC | 284434 |
rs753946273 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16799473 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCACC | 284434 |
rs753951190 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16725507 | CTCCTGCAGGCAAAG[A/G]TAACTAGCTAGAGTT | 284434 |
rs753987400 | snp | A/G | 1.64895e-05 | 0.00287132 | intron-variant | NWD1 | GRCh38.p7 | 19:16779313 | GACACAGGAACTGAG[A/G]TCATTGCTGTTGCCT | 284434 |
rs754022128 | snp | A/G | 1.67105e-05 | 0.0028905 | intron-variant | NWD1 | GRCh38.p7 | 19:16808156 | GTGGCCCGCCTCCCC[A/G]TGTTCATGCTAGACC | 284434 |
rs754049505 | in-del | -/AAA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16728944 | GCATGACTCCATCTC[-/AAA]AAAAAAAAAAAAAAA | 284434 |
rs754074143 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16762535 | CTCCTGCCTGGGCAA[C/T]AGAGAGAAACTCTGT | 284434 |
rs754088747 | snp | A/G | 2.08971e-05 | 0.00323236 | intron-variant | NWD1 | GRCh38.p7 | 19:16789237 | AGCTGAGACCAGAGC[A/G]TTCAAAGACAGAATA | 284434 |
rs754120864 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16724522 | TTGTGAAGAGGTTGG[C/G]CAGGATTCAGGTCGC | 284434 |
rs754141440 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754202 | GATCTTCCATCCTTC[C/T]GTCCATTCTCTCTAA | 284434 |
rs754166663 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16727127 | CAGGCTCAACTTACA[C/T]GGGTAGGCCCCAGGG | 284434 |
rs754191734 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16761779 | CCTCTTTGAAATGTA[G/T]GTAAGGAAAGTAAAT | 284434 |
rs754193428 | snp | A/C/T | 0.000119483 | 0.00772852 | missense, synonymous-codon, intron-variant | NWD1 | GRCh38.p7 | 19:16749866 | TGCCCAGGTTCTGGA[A/C/T]GCCCACACCAGGGTG | 284434 |
rs754193455 | snp | A/G | 1.67407e-05 | 0.00289311 | intron-variant | NWD1 | GRCh38.p7 | 19:16763970 | GCCCCCCATCTCAGA[A/G]GACCGAGCCTGGTGA | 284434 |
rs754240972 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16721106 | CTGCCTGTTTTGGCC[A/T]CTCAAAGTGCTGGGA | 284434 |
rs754261388 | in-del | -/TA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16785620 | AAAATGTTCTGAACT[-/TA]TATATATATATACAC | 284434 |
rs754287266 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16774310 | TCCATCAATTCATCT[A/G]TCAAACCACTTTCCT | 284434 |
rs754316022 | snp | C/T | 3.35025e-05 | 0.00409269 | intron-variant | NWD1 | GRCh38.p7 | 19:16765007 | GAGGTAGGCACTTCC[C/T]ACATCCTCCCCCCTT | 284434 |
rs754318208 | snp | C/T | 0.000104029 | 0.00721137 | missense | NWD1 | GRCh38.p7 | 19:16750347 | CACCAACTCTGCACC[C/T]GCCTGGAGCAGACAC | 284434 |
rs754342687 | in-del | -/T | 1.65351e-05 | 0.00287528 | frameshift-variant | NWD1 | GRCh38.p7 | 19:16762081 | GACCTGGAGCCAGGG[-/T]ACCAAGAAGCTCATC | 284434 |
rs754347215 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732794 | CATGCAGCGCTATCC[C/G]TGGCTAACCGGGGAT | 284434 |
rs754361138 | in-del | -/AGC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16752852 | AAAAGTAAAAATATT[-/AGC]TGGGCGTGGTGGCTC | 284434 |
rs754362021 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16724992 | AGCCACTATGCCTAG[C/T]CAAAAATTTTTATTT | 284434 |
rs754371654 | snp | C/T | 1.9062e-05 | 0.00308717 | stop-gained | NWD1 | GRCh38.p7 | 19:16750410 | TACATTGTGTCTTCC[C/T]GGTAAGTCTCTGTGT | 284434 |
rs754401013 | snp | A/C | 1.65411e-05 | 0.00287581 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807767 | AATCAACTGCATGTC[A/C]CTGAGCAAGTGCGAG | 284434 |
rs754401215 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16745842 | GGATCGCTGGAGCCC[A/G]GGAGTTGGAGGCTGC | 284434 |
rs754409523 | snp | A/G | 3.32171e-05 | 0.00407522 | intron-variant | NWD1 | GRCh38.p7 | 19:16773085 | AGGGAGGGTAGAGGG[A/G]GCTCAATCCAGGCAA | 284434 |
rs754432398 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790239 | AGTGACCTTGGTTGT[A/G]TCATTCACCATTCTG | 284434 |
rs754484342 | snp | A/G | 3.42583e-05 | 0.0041386 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16759336 | GCTGCTGCGCTTCCC[A/G]CCCCTGCTGTGGGTG | 284434 |
rs754488841 | snp | G/T | 0.000329451 | 0.0128303 | missense | NWD1 | GRCh38.p7 | 19:16797817 | GGAACATGAAGACAT[G/T]GTGGAGACGGCTGTT | 284434 |
rs754499195 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790253 | TGTCATTCACCATTC[A/T]GAGTCTTATTGCTGC | 284434 |
rs754502117 | snp | A/G | | | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16719205 | CAGTGGCAGGATCTC[A/G]GCTCATTGCAACCTC | 284434 |
rs754515619 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16747561 | TATTTTTTGTAGAGA[C/T]GGGGTTTTGCCGTTT | 284434 |
rs754537258 | in-del | -/GTTG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16778508 | CTTTTTTTTTTTTTT[-/GTTG]GTTGTTGTTGTTGTT | 284434 |
rs754555935 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16788426 | TAGAAAAAATTAGCC[A/G]GGCATGGCGGCAGGT | 284434 |
rs754567343 | snp | C/T | | | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16717921 | GAGGCAATCATATCT[C/T]ACTGCAGCCTTGACT | 284434 |
rs754568520 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16757553 | CACCAAGGTCTCCCA[C/G]CTAGGCTCAAACGCA | 284434 |
rs754579223 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790642 | AACATTAAAAAAAAA[-/T]AAATAAATAAATAAA | 284434 |
rs754606138 | snp | A/G | 0.000214615 | 0.0103567 | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16745031 | GCATACTTGAGGCTG[A/G]GTAATTTACAAAGGA | 284434 |
rs754630479 | snp | C/T | 3.30251e-05 | 0.00406343 | utr-variant-3-prime, missense | NWD1 | GRCh38.p7 | 19:16815040 | CAGGCACCCTGCTGA[C/T]AGTCCAGTTTGTCCA | 284434 |
rs754633090 | snp | A/C | 6.5962e-05 | 0.00574253 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16779452 | TGTGATCCACATGCT[A/C]ACTGGACACACAGGT | 284434 |
rs754646171 | snp | A/G | 3.38043e-05 | 0.00411109 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749930 | TCTTGCAGAAACTTC[A/G]AGTCTCTCGTGCTCC | 284434 |
rs754653910 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16769585 | GTGTATGACTCACTC[-/T]CCTGGGAGATGCTTG | 284434 |
rs754661134 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16724574 | AGATCATGGCTGGAC[A/G]TGGGGCCTCACACCT | 284434 |
rs754665299 | in-del | -/T | 3.29788e-05 | 0.00406058 | intron-variant | NWD1 | GRCh38.p7 | 19:16812891 | GATTGAGCTTCGATC[-/T]GGAGAGAAAAGGCTC | 284434 |
rs754688171 | snp | C/T | 1.6504e-05 | 0.00287258 | intron-variant | NWD1 | GRCh38.p7 | 19:16788954 | TGTTCCCAGCTAATA[C/T]ACTCTCCCCTACCCT | 284434 |
rs754696189 | snp | C/T | 1.64757e-05 | 0.00287012 | missense | NWD1 | GRCh38.p7 | 19:16791450 | TGGCCTCCCAGGCCA[C/T]ACTGCTGACAGTGTC | 284434 |
rs754701906 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754203 | ATCTTCCATCCTTCC[A/G]TCCATTCTCTCTAAA | 284434 |
rs754719710 | in-del | -/CTCCTC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16814741 | TTCCTTCTCCTCCTT[-/CTCCTC]CAACAATAATATTTA | 284434 |
rs754774433 | in-del | -/TTATTTATTTAT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16755691 | CACATCCAGCCTTAT[-/TTATTTATTTAT]TTATTTATTTATTTA | 284434 |
rs754805983 | in-del | -/TATC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16755161 | ATCAATAAATCTCTA[-/TATC]TATCTCTCTATTTCT | 284434 |
rs754821899 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16723868 | GCCCGGCTAATTTTT[A/G]TATTTTTAGTAGAGA | 284434 |
rs754845893 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764330 | TCTGTTCATCCACCT[A/G]TCCATCCATCCATCC | 284434 |
rs754910128 | snp | C/T | 3.29772e-05 | 0.00406048 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16759265 | AAGGATGTTTTGTCC[C/T]TGGACGACGAGGTCC | 284434 |
rs754921300 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16799167 | TAGGTTTATGAATGG[C/G]CTGAAGTGTATTTCT | 284434 |
rs754931018 | in-del | -/C | 1.64909e-05 | 0.00287144 | frameshift-variant, utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16797855 | TGAGAACAACCTGAT[-/C]CATCACGGGGTCCCT | 284434 |
rs754959785 | snp | C/G | 1.96728e-05 | 0.00313625 | intron-variant | NWD1 | GRCh38.p7 | 19:16765244 | GGGCACTGACTTCTA[C/G]AAACATGCTCTCCTC | 284434 |
rs754983174 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16733213 | GTGCCAGATTGGGAT[A/G]CTGTCTTTAAAAAAA | 284434 |
rs754996345 | in-del | -/TCACCATGTTGGCCAGGC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16813672 | AGTAGAGGTAGGGTT[-/TCACCATGTTGGCCAGGC]TGGTCTTGAACTCCT | 284434 |
rs755006819 | snp | C/T | 1.64792e-05 | 0.00287042 | missense | NWD1 | GRCh38.p7 | 19:16807853 | GGGACCCCTGCCCGG[C/T]CATCGATGGGCCAAG | 284434 |
rs755023343 | snp | C/T | 1.6489e-05 | 0.00287128 | intron-variant | NWD1 | GRCh38.p7 | 19:16779320 | GAACTGAGATCATTG[C/T]TGTTGCCTCTGTGTG | 284434 |
rs755085286 | in-del | -/CCAT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16774148 | CATCTACTGCCCCAT[-/CCAT]CCATCCATCCATCCA | 284434 |
rs755132934 | snp | A/C | 1.67433e-05 | 0.00289333 | intron-variant | NWD1 | GRCh38.p7 | 19:16808162 | CGCCTCCCCATGTTC[A/C]TGCTAGACCCAGGCA | 284434 |
rs755182156 | snp | C/T | 3.29696e-05 | 0.00406001 | missense, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800042 | GATGCTCATAGGTCC[C/T]GGGTGCCTGCACCAT | 284434 |
rs755182529 | snp | A/G | 3.32668e-05 | 0.00407827 | missense | NWD1 | GRCh38.p7 | 19:16762115 | CTGCCACTTGTGGGG[A/G]AACCACTGAACTTGG | 284434 |
rs755185898 | snp | C/G | 1.64727e-05 | 0.00286986 | intron-variant, synonymous-codon | NWD1 | GRCh38.p7 | 19:16812807 | CAAGTATGTGTACGT[C/G]GGCTTAAAGGATCGC | 284434 |
rs755226327 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16722278 | CACTCCAGCCTGGGC[C/G]ACAGAGCAAGACTTG | 284434 |
rs755237671 | snp | C/T | 3.32978e-05 | 0.00408017 | missense | NWD1 | GRCh38.p7 | 19:16750099 | GGGTGCTCCTGGACC[C/T]GGAGGCCTACTGGGA | 284434 |
rs755286612 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754927 | TCTATCTCTATATAT[C/T]TATATATTTCTCTAT | 284434 |
rs755347777 | snp | A/C | 1.66435e-05 | 0.0028847 | stop-gained | NWD1 | GRCh38.p7 | 19:16807725 | GCAGGACGTGATATG[A/C]ATTCCCCCTCCCGAG | 284434 |
rs755366503 | snp | C/T | 1.66969e-05 | 0.00288932 | intron-variant | NWD1 | GRCh38.p7 | 19:16765012 | AGGCACTTCCCACAT[C/T]CTCCCCCCTTCTCTC | 284434 |
rs755392237 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16804971 | CTGGAACCACAGGTG[C/T]ACCACCATGCCTGAC | 284434 |
rs755401918 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16792039 | CTTCTTAATCGTAGG[C/G]ATTTGCAGTTCAGCA | 284434 |
rs755419674 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16793516 | CAGGCGTGACCCACT[G/T]TACCTGGCCAGAATT | 284434 |
rs755454648 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16721117 | GGCCTCTCAAAGTGC[A/T]GGGATTAGAGGTGTG | 284434 |
rs755485664 | snp | A/C/G | 5.21983e-05 | 0.00510851 | missense | NWD1 | GRCh38.p7 | 19:16773302 | GGACCCCTCCGGGCA[A/C/G]CTCTCAGCGGCTGTC | 284434 |
rs755542219 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16720549 | CTAGGGGACATTGCA[A/G]TGTCTAGGGAGACTT | 284434 |
rs755556770 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16804170 | GAGCAAGAATGCAGG[C/G]TCAGCTAAAGTCCCT | 284434 |
rs755600947 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16727172 | AGAGGTTGGCTGGTC[C/T]CCGGGCCCCAATGCC | 284434 |
rs755615732 | snp | A/C | 3.31197e-05 | 0.00406925 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16765137 | CTCCCCTGAGGTTGG[A/C]CTGGTCCGTGAAGCC | 284434 |
rs755638592 | snp | A/C | 2.36616e-05 | 0.00343951 | intron-variant | NWD1 | GRCh38.p7 | 19:16750433 | CTCTGTGTTTTGAAA[A/C]TCTTATTTATTTATT | 284434 |
rs755646205 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16768980 | ATCCTCGGAGGTCTG[C/T]CTACTTTGGATTCAT | 284434 |
rs755648675 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16756307 | ATTCATGAAGTGGAA[G/T]TGGATATCACAAAGG | 284434 |
rs755667098 | snp | A/G | 1.64879e-05 | 0.00287118 | missense | NWD1 | GRCh38.p7 | 19:16759253 | GAGGCGGAGCTGAAG[A/G]ATGTTTTGTCCCTGG | 284434 |
rs755670452 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787092 | GCCTTCCAAATTGTA[C/T]GTTTTGCTTAGCAAA | 284434 |
rs755673954 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16812555 | ATGCCTGTAATCCTA[G/T]CTACTTGGGAGGCTG | 284434 |
rs755725829 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16799805 | GAGCCACCGCGCCTG[A/G]CCCAATGGGCTGAAG | 284434 |
rs755756403 | snp | C/G/T | 0.000131839 | 0.0081182 | missense | NWD1 | GRCh38.p7 | 19:16807850 | CCGGGGACCCCTGCC[C/G/T]GGTCATCGATGGGCC | 284434 |
rs755764453 | snp | A/G | 1.65712e-05 | 0.00287843 | synonymous-codon, missense | NWD1 | GRCh38.p7 | 19:16797745 | AGGCTTTGGAAGATC[A/G]GTGCGGATATTCTTG | 284434 |
rs755798410 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16811697 | AACCTTTCTATCCAA[A/T]CTCTATGGAGGTGTG | 284434 |
rs755826807 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16726227 | TCGGCCTCCCAAAGT[C/G]CTGGGATTACAGGCG | 284434 |
rs755839382 | snp | A/G | 4.94572e-05 | 0.00497254 | missense, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800027 | GTCTGGGATCTCAGC[A/G]ATGCTCATAGGTCCC | 284434 |
rs755844911 | snp | A/G | 9.95867e-05 | 0.00705574 | missense | NWD1 | GRCh38.p7 | 19:16762109 | ATCACTCTGCCACTT[A/G]TGGGGAAACCACTGA | 284434 |
rs755845600 | in-del | -/C | 3.33728e-05 | 0.00408476 | intron-variant | NWD1 | GRCh38.p7 | 19:16765015 | CACTTCCCACATCCT[-/C]CCCCCTTCTCTCCCT | 284434 |
rs755869213 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16742173 | TGAGATCAAGAATTC[A/G]AGACCAGCCTGGCCA | 284434 |
rs755870000 | snp | C/T | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748128 | AGTTGGGATTACAGG[C/T]GTGCGGCATCACGCT | 284434 |
rs755876939 | in-del | -/TCTT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16761351 | TGTTCCCTTTCTTTC[-/TCTT]TCTTTCTTTCTTTCC | 284434 |
rs755885608 | snp | A/G | 1.64765e-05 | 0.00287019 | missense, stop-gained | NWD1 | GRCh38.p7 | 19:16797790 | CTTTCGCCGATTCAT[A/G]GCCATGGATCTGGAA | 284434 |
rs755935157 | in-del | -/A | 2.17394e-05 | 0.00329685 | frameshift-variant, intron-variant | NWD1 | GRCh38.p7 | 19:16794479 | TTTCCTCCAAAGGGG[-/A]CAGATTGCTGGAGAA | 284434 |
rs755964182 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16735413 | CGGGAGGCTGAGGCA[A/G]GAGAATTGCTTGAAC | 284434 |
rs755971373 | snp | G/T | 1.67027e-05 | 0.00288982 | missense | NWD1 | GRCh38.p7 | 19:16750048 | TCATCCTCTCAGCTT[G/T]CTCGGGGGCACTGGG | 284434 |
rs756011508 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16774849 | ATCTTCCATTCATTC[A/G]CTTACGCCTCCACCC | 284434 |
rs756016333 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16803756 | ACCCCAACTCTACTT[-/A]AAAAAAAAAAAAAAA | 284434 |
rs756026611 | snp | C/T | 1.66499e-05 | 0.00288525 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750091 | CTTGCAGCGGGTGCT[C/T]CTGGACCCGGAGGCC | 284434 |
rs756038608 | in-del | -/AAA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16746691 | AAAAAACAAAAAACA[-/AAA]ACAAAAAAAAACAGT | 284434 |
rs756057540 | snp | A/G | 1.65304e-05 | 0.00287488 | splice-acceptor-variant | NWD1 | GRCh38.p7 | 19:16765033 | CCCTTCTCTCCCTCA[A/G]GCAGCATGAGCTGGA | 284434 |
rs756087708 | snp | A/G | 1.6476e-05 | 0.00287014 | missense | NWD1 | GRCh38.p7 | 19:16791437 | TGCATGGCCGTGCTG[A/G]CCTCCCAGGCCACAC | 284434 |
rs756218108 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16799060 | GAACACACTTTGGGA[A/G]CTGCTCTGGAAGCTG | 284434 |
rs756304107 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764065 | TCCTCCTAAGGCAGA[A/G]GTTCTCACAAGGGGC | 284434 |
rs756307957 | snp | A/C | 1.71402e-05 | 0.00292742 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16773292 | GCCCCCGGGAGGACC[A/C]CTCCGGGCAACTCTC | 284434 |
rs756345904 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16808288 | GGCGCAGTGGCTCAC[A/G]CCTGTAATCCCAGTA | 284434 |
rs756358334 | snp | A/G | 0.00013164 | 0.00811187 | intron-variant | NWD1 | GRCh38.p7 | 19:16736767 | TGAGTGTCTTGGGAG[A/G]AATGGGTTAGCTCTT | 284434 |
rs756358468 | in-del | -/TCTT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16761354 | CCCTTTCTTTCTCTT[-/TCTT]TCTTTCTTTCTTTCC | 284434 |
rs756420229 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16757627 | GCGGGTCCTCTGGGA[A/G]TGCCAAGTGAGGTGC | 284434 |
rs756430741 | snp | C/T | 1.77436e-05 | 0.0029785 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749131 | TCCCACCTTCCCCAC[C/T]TTGGCAGTCATTGAG | 284434 |
rs756432984 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16720459 | ACTAAAGTACAGGAC[A/G]TGCAAAGGCCCTGAG | 284434 |
rs756467114 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16723754 | GCCAAGGCTGGGTGT[A/G]GTGTGATCTCAGCTC | 284434 |
rs756526921 | snp | A/C/G | 3.29485e-05 | 0.00405874 | utr-variant-3-prime, missense | NWD1 | GRCh38.p7 | 19:16815127 | ATGGTTATCTGATCC[A/C/G]AGAGAATTTCCAGTG | 284434 |
rs756533259 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16802775 | GGAGGCCAAGGCAGG[C/T]GCATCATTTGAGGTC | 284434 |
rs756540559 | snp | G/T | 1.64863e-05 | 0.00287104 | missense | NWD1 | GRCh38.p7 | 19:16763874 | CGGTTGCAAACCTGC[G/T]GAAGCTGAAGGAGTT | 284434 |
rs756545476 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16804013 | GTTGGCAATCTGGTT[A/G]TTTCCGTTTGGCCTG | 284434 |
rs756548539 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16722789 | GGAGCTTTAAGTCAC[A/G]TGATATTGGTTGACC | 284434 |
rs756580912 | in-del | -/TTCCTTCCTTCC/TTCCTTCCTTCCTTCCTTCCTTCCTTCC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16736209 | TCCTTCCTTCCTTCT[lengthTooLong]TTCCTTCCTTCCTTC | 284434 |
rs756596307 | snp | C/G | | | downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16818332 | AAGGGATGCCGAAAA[C/G]CTCAGCAATCATGAC | 284434 |
rs756600818 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16805685 | AGCAAACAAGCACCT[C/T]GAGAATTGTAACCTC | 284434 |
rs756605287 | snp | A/G | 5.14073e-05 | 0.00506961 | missense | NWD1 | GRCh38.p7 | 19:16750333 | CAGAGGAAGCCACGC[A/G]CCAACTCTGCACCCG | 284434 |
rs756630809 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16771668 | TGCAAAGCCCCTTGA[G/T]TGACAACCTGTGGCT | 284434 |
rs756653578 | in-del | -/A | 1.65051e-05 | 0.00287267 | frameshift-variant | NWD1 | GRCh38.p7 | 19:16789054 | AGGATTACACGCTGC[-/A]CTTGTGGAACTTACT | 284434 |
rs756667011 | snp | G/T | 2.39375e-05 | 0.0034595 | intron-variant | NWD1 | GRCh38.p7 | 19:16794453 | GACAGGCATCCCTGG[G/T]TCTGCACAGGTTTCC | 284434 |
rs756671245 | in-del | -/TCCTC | 1.65954e-05 | 0.00288053 | frameshift-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749472 | GGGCCAATCACCAGG[-/TCCTC]ACACGCCTCCGTGAG | 284434 |
rs756780862 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16780575 | CACAAGAGCAGTCCA[A/G]TAGGGAAATAGGCTA | 284434 |
rs756874132 | snp | G/T | 1.99162e-05 | 0.00315558 | intron-variant | NWD1 | GRCh38.p7 | 19:16750417 | TGTCTTCCCGGTAAG[G/T]CTCTGTGTTTTGAAA | 284434 |
rs756882383 | in-del | -/AA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16728945 | CATGACTCCATCTCA[-/AA]AAAAAAAAAAAAAAA | 284434 |
rs756927590 | snp | G/T | 3.52032e-05 | 0.00419528 | intron-variant | NWD1 | GRCh38.p7 | 19:16794568 | GGTAGCGTTTAGCTC[G/T]CATTTGGAGTAGTGA | 284434 |
rs756944083 | snp | A/G | 0.000832755 | 0.0203883 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16731220 | GAGGGAAGCCCTGCA[A/G]AGCACTGCCTACCCT | 284434 |
rs757004574 | in-del | -/TT/TTT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16731610 | AGCCCAGCCCCATGC[-/TT/TTT]TTTTTTTTTTTTGAG | 284434 |
rs757027729 | snp | A/G | 1.64789e-05 | 0.0028704 | missense | NWD1 | GRCh38.p7 | 19:16808048 | AGGTCAGCCACAAGG[A/G]GCAGCTGGTGGTCAG | 284434 |
rs757039549 | snp | C/T | 4.95127e-05 | 0.00497533 | missense | NWD1 | GRCh38.p7 | 19:16807786 | AGCAAGTGCGAGGAC[C/T]GCCTGGCCATCGCCT | 284434 |
rs757043963 | snp | A/G | 1.68414e-05 | 0.0029018 | missense | NWD1 | GRCh38.p7 | 19:16749961 | TGCTGGATGCTATGG[A/G]TGACCTGGACTCTGT | 284434 |
rs757112691 | snp | A/C/G | 5.01026e-05 | 0.00500492 | intron-variant | NWD1 | GRCh38.p7 | 19:16761962 | CAGGTCTATCAGTCT[A/C/G]TATACCCTCTCTGTA | 284434 |
rs757118465 | in-del | -/ATT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16793399 | CCCCATGCCTGGCTA[-/ATT]ATTATTATTATTATT | 284434 |
rs757169841 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790964 | AGGCCGGGTGCAGTG[C/G]CTCACACTCATAATC | 284434 |
rs757224904 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16799569 | TTGCGTGCAATGGCA[C/T]GATCTTGGCTCATTG | 284434 |
rs757244606 | snp | A/C | 1.64841e-05 | 0.00287085 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16789133 | CGCTGAACCTCAGAT[A/C]TGGAACCTTCATGTG | 284434 |
rs757246652 | snp | C/T | 1.64844e-05 | 0.00287087 | synonymous-codon, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800023 | CAAGGTCTGGGATCT[C/T]AGCGATGCTCATAGG | 284434 |
rs757264930 | snp | C/T | 4.97253e-05 | 0.004986 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16791595 | AGGAAAGCTTGTTAC[C/T]GGGTTTAGCAATGGC | 284434 |
rs757270022 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16798468 | ACACAAAAATTAGCC[A/G]GGCGTCATGGCATGT | 284434 |
rs757272634 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16756184 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 284434 |
rs757275009 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16795945 | CTCTTGTCCCGTGTC[C/G]AAGAAGAATGAGGTC | 284434 |
rs757277796 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16812449 | CAAGGCTAGTGGATC[A/G]CCTGAGGTGAGGAGT | 284434 |
rs757308221 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751226 | CAAAACTCGATCTCA[-/A]AAAAAAAAAAAAAAA | 284434 |
rs757312418 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16773475 | CCCTGCTGTCTCATG[C/G]TGAATCAGCTCTCTC | 284434 |
rs757341864 | snp | C/T | 1.78745e-05 | 0.00298947 | missense | NWD1 | GRCh38.p7 | 19:16807637 | TCAGGTGTCTGGAGG[C/T]TGCTGAGCAGCGCAA | 284434 |
rs757356017 | in-del | -/TCCC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16753800 | TCATCCATCCATCAA[-/TCCC]TCCCTCCCTCCCTCC | 284434 |
rs757377319 | snp | C/T | 1.65996e-05 | 0.00288089 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749486 | GTCCTCACACGCCTC[C/T]GTGAGCTGGATACGG | 284434 |
rs757394915 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16795136 | TTTGCCAAGCTGGGA[A/G]CAGGGGGCACCCCAT | 284434 |
rs757411822 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16762559 | ACTCTGTCTCAAAAA[C/T]AAACAAACAAACAAA | 284434 |
rs757421097 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16806685 | CACTGCACTCCAGCC[C/T]GGGCAACAGAGTGAG | 284434 |
rs757439787 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16775267 | CTTAGTGGGAAAGAG[G/T]GTGTATTTGTTAGAA | 284434 |
rs757450072 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16807531 | ACCACCAGGGAAGCA[A/G]GGCTGCTGTGATTCA | 284434 |
rs757464304 | snp | A/G | 2.83178e-05 | 0.00376272 | intron-variant | NWD1 | GRCh38.p7 | 19:16794426 | TGTAACCCTTAACCC[A/G]TGGAAGTGCCTGACA | 284434 |
rs757482769 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16722857 | GGTCAATCATGTCTA[C/T]GTGACCAACTCCCAA | 284434 |
rs757510617 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16741186 | AAGGGGGAGGGGACA[A/G]CCTTATCCCCCTTCG | 284434 |
rs757519091 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16797472 | AGTAGCTGGGATTAC[A/G]TGCATGTGCCACCAC | 284434 |
rs757542502 | snp | C/T | 4.94205e-05 | 0.0049707 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807959 | CATGACCAATGGGGA[C/T]CTCTTTCTTTACGAG | 284434 |
rs757566024 | snp | G/T | 1.65408e-05 | 0.00287578 | stop-gained | NWD1 | GRCh38.p7 | 19:16773197 | CATCCAGCACTGGTG[G/T]GACAGCTATGCCAAC | 284434 |
rs757579478 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16730831 | TCCAGGAGTTCAAGA[C/T]CAGCCTAGGAAACAT | 284434 |
rs757585274 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16729958 | GAAAGAAAGATTTGT[A/C]CCTGTTATTCTCTAG | 284434 |
rs757609952 | snp | A/G | 8.24069e-05 | 0.00641846 | missense | NWD1 | GRCh38.p7 | 19:16779436 | ACATGGAAGAGCAGC[A/G]TGTGATCCACATGCT | 284434 |
rs757625266 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16735261 | GTAATCCTAACATTT[C/T]GGGAGGCTGAGGCAG | 284434 |
rs757633612 | snp | C/T | 0.000160167 | 0.00894749 | synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744579 | GTTTCCTCCCACCTA[C/T]GTCCTGCAGGCACCA | 284434 |
rs757647445 | snp | C/G | 1.64735e-05 | 0.00286993 | intron-variant, missense | NWD1 | GRCh38.p7 | 19:16812837 | CTCTATACTTGTTTG[C/G]AGTGTGCTGGATGGT | 284434 |
rs757654810 | snp | A/G | 3.31846e-05 | 0.00407323 | intron-variant | NWD1 | GRCh38.p7 | 19:16779512 | CTTCCATAGTGAAAA[A/G]TTGGTTCTCAGAGCC | 284434 |
rs757660714 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16757771 | ATCATAGAATTTTGC[A/C]GGCCAGGTGCAGTGG | 284434 |
rs757682269 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16801319 | TGGCATGTGCTTGTT[G/T]TTCTAGCTATTTTGG | 284434 |
rs757700506 | snp | A/C | 1.65732e-05 | 0.00287859 | missense | NWD1 | GRCh38.p7 | 19:16815031 | TCACCCTTACAGGCA[A/C]CCTGCTGACAGTCCA | 284434 |
rs757702074 | snp | A/G | 0.000163975 | 0.0090532 | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744767 | CAAGAAACTGACCAC[A/G]TGTTCAGAATATCCA | 284434 |
rs757707682 | snp | A/G | 1.64866e-05 | 0.00287106 | missense | NWD1 | GRCh38.p7 | 19:16763868 | CACATACGGTTGCAA[A/G]CCTGCGGAAGCTGAA | 284434 |
rs757714077 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782283 | AGCAAGACGTCACCT[A/C]TAAAAAAAAAAAAAA | 284434 |
rs757715696 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16770627 | CCTCCCCCTGCCCCA[C/T]AGCCCTCAGTTTTCC | 284434 |
rs757733064 | snp | G/T | 1.6631e-05 | 0.00288362 | intron-variant | NWD1 | GRCh38.p7 | 19:16763789 | GGAGTGAATGAATGG[G/T]TTTGTGTCCAAGCTG | 284434 |
rs757739414 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16814827 | TTCAATCTTAAAAAT[C/T]GCCCTGAGCAGGTGT | 284434 |
rs757768559 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16783254 | TTCCCAGGCTGGTCT[C/T]GAATTCCTGGTATCA | 284434 |
rs757775309 | snp | A/C | 1.81955e-05 | 0.0030162 | intron-variant | NWD1 | GRCh38.p7 | 19:16807549 | CTGCTGTGATTCACT[A/C]TCAGTGTAAGTCATT | 284434 |
rs757776142 | snp | C/T | 1.6759e-05 | 0.00289469 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750185 | GCTGCAAGGAGGACG[C/T]TGAGCCCGGTGCACA | 284434 |
rs757849020 | snp | A/G | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749022 | CAGACTCTGGTGCAC[A/G]TTAATCTTGAGAACC | 284434 |
rs757861496 | in-del | -/C | 5.14134e-05 | 0.00506992 | frameshift-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749646 | ACAGCAAGCAGCACA[-/C]CCCCCTGGTACTCTT | 284434 |
rs757875237 | in-del | -/TGGGTCCTG | 1.65464e-05 | 0.00287627 | cds-indel | NWD1 | GRCh38.p7 | 19:16762084 | TGGAGCCAGGGTACC[-/TGGGTCCTG]AAGAAGCTCATCACT | 284434 |
rs757882385 | snp | A/G | 1.68077e-05 | 0.00289889 | missense, utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16799931 | CTGGACATCCTGGAA[A/G]GCGTCGGGGCCCCCG | 284434 |
rs757897803 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16778247 | TTTCTTAGTGTCTAG[A/G]CCCACGTTTTCTCCA | 284434 |
rs757906436 | snp | A/G | 3.29794e-05 | 0.00406061 | intron-variant | NWD1 | GRCh38.p7 | 19:16788975 | CCCCTACCCTGGCCT[A/G]CTGCAGGAGAGGTGA | 284434 |
rs757924985 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16779219 | GCAGCTTTGGGCAAG[C/G]GACCAAATCTCTCTG | 284434 |
rs757951041 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790400 | GTAATATCAGTGCAT[A/G]TAAATCATGCTGCCC | 284434 |
rs757951080 | snp | C/T | 0.000378916 | 0.0137592 | missense | NWD1 | GRCh38.p7 | 19:16789117 | GAGGCTCAAAAAATC[C/T]CGCTGAACCTCAGAT | 284434 |
rs757951904 | snp | G/T | 6.95169e-05 | 0.00589522 | missense, upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749152 | AGTCATTGAGTGGGA[G/T]ATAGAGCGGAGCCTG | 284434 |
rs757960963 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16727682 | GTCTCAGGTAAGGTG[C/G]AGGGTATGGATGGGG | 284434 |
rs757979036 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764589 | CATTCATCTACCTTT[C/T]TGGTCATCCATCCAT | 284434 |
rs758021820 | in-del | -/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16769268 | GGAGTTTGAGACCAG[-/C]CTGGCCAACAGGGTG | 284434 |
rs758043234 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16759592 | TTTTTAAAATTGAGT[A/T]GAGGCTGGAAGCAGT | 284434 |
rs758051323 | snp | C/T | 6.98361e-05 | 0.00590874 | missense | NWD1 | GRCh38.p7 | 19:16807664 | GCAAGCTCCTATTTA[C/T]GGGCCTCGTGTCGGG | 284434 |
rs758076539 | snp | C/T | 8.24804e-05 | 0.00642132 | missense, upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749225 | AGAGAGATCCAAGAC[C/T]TCCACAAACACATCC | 284434 |
rs758085338 | snp | A/G | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748721 | CCCAGCTACTCGGGA[A/G]GCTGAGGTGGAAGGA | 284434 |
rs758106322 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16745334 | AAGATGAGATTTGGG[G/T]GAAGACACAGCCAAA | 284434 |
rs758114759 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16769719 | GAGCTCAGCTAAATG[C/T]GATTCCTCAGAGAAG | 284434 |
rs758137418 | snp | C/T | 3.30562e-05 | 0.00406534 | utr-variant-3-prime, missense | NWD1 | GRCh38.p7 | 19:16815247 | TTGCAGCTGCAGGAG[C/T]TCCCCAGGACTTGGA | 284434 |
rs758163771 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16798332 | ATTGATAAATAGACT[C/G]TGCACAGTGGCTCAT | 284434 |
rs758178850 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16785984 | ATCTTCCTGCCTCAG[A/C]CTCCCAAGTAGCTGA | 284434 |
rs758211491 | snp | A/G | 1.64773e-05 | 0.00287026 | missense | NWD1 | GRCh38.p7 | 19:16807861 | TGCCCGGTCATCGAT[A/G]GGCCAAGATACACCT | 284434 |
rs758216594 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16811229 | TTAATTAAATACAAT[C/T]ATAGCTAACATCCGT | 284434 |
rs758222699 | snp | C/G | 2.00182e-05 | 0.00316365 | missense | NWD1 | GRCh38.p7 | 19:16759355 | CTGCTGTGGGTGCGG[C/G]TTCGTCGGGATCTGG | 284434 |
rs758240550 | snp | A/G | 1.66134e-05 | 0.00288208 | intron-variant | NWD1 | GRCh38.p7 | 19:16773083 | GCAGGGAGGGTAGAG[A/G]GGGCTCAATCCAGGC | 284434 |
rs758244616 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16756045 | TATGTATTACAGACT[A/G]TATTCCTACAACAAA | 284434 |
rs758274808 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807944 | CCGCGTGGTCTACAG[C/T]ATGACCAATGGGGAC | 284434 |
rs758362306 | snp | A/G | 3.36005e-05 | 0.00409867 | intron-variant | NWD1 | GRCh38.p7 | 19:16761954 | GGGTCACCCAGGTCT[A/G]TCAGTCTGTATACCC | 284434 |
rs758398148 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16724620 | TGGGAGGCTCAGGTG[A/G]GAGGATCGTTTGTTG | 284434 |
rs758400100 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16740349 | ATTATTATTATTATT[A/G]TTTTGAGATGGAGTC | 284434 |
rs758429944 | snp | C/T | 1.64985e-05 | 0.0028721 | missense, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800085 | CCGGCCTCACCGCAG[C/T]GTCCCACAATGGAAG | 284434 |
rs758437985 | in-del | -/TTTT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16760261 | TTTTATTTTATTTTA[-/TTTT]ATTTTATTTTATGTA | 284434 |
rs758446696 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754924 | TGTCTATCTCTATAT[-/A]ATCTATATATTTCTC | 284434 |
rs758457446 | snp | A/C | 1.66388e-05 | 0.00288429 | missense | NWD1 | GRCh38.p7 | 19:16750105 | TCCTGGACCCGGAGG[A/C]CTACTGGGAGGTGAA | 284434 |
rs758469567 | snp | A/G | 8.06565e-05 | 0.00634994 | intron-variant | NWD1 | GRCh38.p7 | 19:16762188 | ACCTCCACCCTGCCT[A/G]GCATTGCTCACCTCC | 284434 |
rs758480936 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16720633 | TGATCTCAGTTACTG[C/T]AAGCTCTGCCTCCCA | 284434 |
rs758526375 | snp | A/C | 1.67753e-05 | 0.00289609 | intron-variant | NWD1 | GRCh38.p7 | 19:16815017 | TTGTGTCCTTCTCTT[A/C]ACCCTTACAGGCACC | 284434 |
rs758553493 | snp | A/G | 4.04408e-05 | 0.00449653 | intron-variant | NWD1 | GRCh38.p7 | 19:16773345 | CTCCCCAGCATAGCA[A/G]AAATCCCAGCAGGCA | 284434 |
rs758581857 | snp | C/T | 1.77307e-05 | 0.00297742 | intron-variant, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800184 | AAGGTATAAGTATGG[C/T]CATTTTTGTGGGTAA | 284434 |
rs758587677 | in-del | -/C | 6.41612e-05 | 0.00566361 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815332 | CTGATAGTGTAAAAA[-/C]AATAAAAATAAAAAA | 284434 |
rs758616242 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16806581 | CTGGGCGTGGTGGCC[C/T]GAGCCTGTAGTCCCA | 284434 |
rs758628488 | snp | G/T | 3.29511e-05 | 0.00405887 | missense | NWD1 | GRCh38.p7 | 19:16791473 | ACAGTGTCCAGGGAT[G/T]GTGTGGTCAGTCTGT | 284434 |
rs758642170 | snp | C/G | 1.68624e-05 | 0.0029036 | missense | NWD1 | GRCh38.p7 | 19:16750252 | ACCCAGGGCGGCTGA[C/G]GCTGGCGTTTGAGGA | 284434 |
rs758751443 | snp | A/G | 1.65537e-05 | 0.0028769 | missense | NWD1 | GRCh38.p7 | 19:16791582 | CAGTCCAGAAGCAAG[A/G]AAAGCTTGTTACCGG | 284434 |
rs758759426 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16746001 | AACTCCTTGCACAGT[C/T]GAAAATCTGTGTATA | 284434 |
rs758777606 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16727236 | ACTGCGCTCTGAGGA[C/T]GAGGAGCTGGGAAGA | 284434 |
rs758777976 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16743567 | AGGCTATAAGGGCGG[C/T]CAACTTCACCTCCAT | 284434 |
rs758782698 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16739591 | TCCATCTTGAACCAG[A/G]CATCACCCCTCTACT | 284434 |
rs758790460 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16769219 | ATAATCCCAGCACTT[C/T]GGGAGGCTGAGGCAG | 284434 |
rs758793239 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16781056 | TTTTGCATTTGTCGA[C/T]CTCAGATCCTAAGTA | 284434 |
rs758829812 | snp | C/G | 8.62478e-05 | 0.00656631 | synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749659 | CACCCCCCTGGTACT[C/G]TTTGGGCCCCCAGGC | 284434 |
rs758844189 | snp | A/G | 1.64792e-05 | 0.00287042 | missense | NWD1 | GRCh38.p7 | 19:16779429 | GTGTGGGACATGGAA[A/G]AGCAGCATGTGATCC | 284434 |
rs758847860 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16781627 | TCTCAAAAAAAAAAG[C/G]AAGACTACATTTATT | 284434 |
rs758865519 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16742477 | TCCCTTTCTCCGTGG[C/T]CAGCCCTTAAGCCAT | 284434 |
rs758868707 | snp | C/T | 8.23608e-05 | 0.00641667 | intron-variant, missense | NWD1 | GRCh38.p7 | 19:16812820 | GTGGGCTTAAAGGAT[C/T]GCTCTATACTTGTTT | 284434 |
rs758887166 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16722715 | AATGGGATAAGGGTG[C/T]CTTTGTTTACCTGGA | 284434 |
rs758887196 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751518 | AGGAAGGAAGGAAAG[A/C]GGCCTGGCATGGTGG | 284434 |
rs758899223 | snp | A/G | 1.64841e-05 | 0.00287085 | intron-variant | NWD1 | GRCh38.p7 | 19:16779335 | CTGTTGCCTCTGTGT[A/G]GCTGCAGGCATCACC | 284434 |
rs758910754 | snp | C/T | 1.66095e-05 | 0.00288175 | synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749524 | GGAGTTGGCGTGGCT[C/T]TACCAAGAGATCCGC | 284434 |
rs758943904 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16772271 | TATAGAGGCTGTGGC[C/T]GGAAGATCGCTTGAG | 284434 |
rs758985517 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16793641 | GAATGCAGTGGCGCA[A/G]TCTCGGCTCACTGAA | 284434 |
rs758993188 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732934 | TCCCATTTGGTTAAA[A/C]GATGAGGCCGGGCAC | 284434 |
rs759026561 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16759126 | GTGATGTGCTGGACA[A/C]CGCGCGGGTGGCTGT | 284434 |
rs759082077 | snp | A/T | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817740 | GGAGCCCTGAAAAAA[A/T]TAGCTACTCTTTGCC | 284434 |
rs759082341 | snp | G/T | 2.22299e-05 | 0.00333383 | missense, intron-variant | NWD1 | GRCh38.p7 | 19:16794514 | CCAGATGCTGTGAGG[G/T]TCCTGGTGGTCTCTG | 284434 |
rs759098401 | snp | C/T | 0.000101247 | 0.0071143 | intron-variant | NWD1 | GRCh38.p7 | 19:16761946 | AGCTTGATGGGTCAC[C/T]CAGGTCTATCAGTCT | 284434 |
rs759119230 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16771316 | TTAGCCGGGTGTGGT[A/G]GTGCATGCCTGTAAT | 284434 |
rs759136923 | snp | A/G | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815684 | CTGGGAGAATGCAGA[A/G]CTCTAATCGGCTAGA | 284434 |
rs759139370 | snp | C/T | 1.68995e-05 | 0.00290679 | missense | NWD1 | GRCh38.p7 | 19:16773278 | GGAGGATTCCTCCAG[C/T]CCCCGGGAGGACCCC | 284434 |
rs759168956 | snp | C/T | 1.65162e-05 | 0.00287365 | missense | NWD1 | GRCh38.p7 | 19:16808105 | TCTGGGACCTGCAGG[C/T]ACGCAAGTGGAAATT | 284434 |
rs759173240 | in-del | -/TAT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16738627 | CTATTTTCTGAGATC[-/TAT]TTTCTGAGACCTAAA | 284434 |
rs759179068 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16744114 | TAAATTGTGGCTGGG[G/T]ACAGTGGCTCACGAC | 284434 |
rs759188419 | snp | C/T | 1.6477e-05 | 0.00287024 | missense | NWD1 | GRCh38.p7 | 19:16808008 | TTTCCCTTGGAGACC[C/T]ACAGGAGCCGAGTTG | 284434 |
rs759207349 | snp | C/T | | | synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744648 | AACTTCTGTCCTACG[C/T]TCTGGAGCCCAGGAG | 284434 |
rs759220842 | snp | A/G | 4.94792e-05 | 0.00497365 | missense | NWD1 | GRCh38.p7 | 19:16762005 | AGGTGGTCCGTGAGC[A/G]CTACCTGTCAGGATC | 284434 |
rs759231989 | in-del | -/TT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782863 | TTCTTCCTTTTCCTT[-/TT]CTTTCTTTCTTTCTT | 284434 |
rs759238338 | snp | C/T | 1.80445e-05 | 0.00300365 | intron-variant | NWD1 | GRCh38.p7 | 19:16799870 | TCAGATCTGCCCTCC[C/T]GTTCTGCTTCCTCAG | 284434 |
rs759241873 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16730587 | ATGGCTGTGGTGGTG[A/C]CCCTCTATAATCCCA | 284434 |
rs759271171 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754566 | TCCTTCCACCCATTC[C/T]CTCTAAAGTCCATCT | 284434 |
rs759302358 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16803737 | GCCTGGCCAACATGG[C/T]GAAACCCCAACTCTA | 284434 |
rs759322511 | snp | C/G | | | missense | NWD1 | GRCh38.p7 | 19:16791490 | TGTGGTCAGTCTGTG[C/G]AGCTCAGCTACGGGA | 284434 |
rs759350506 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16775195 | ACAATGCATGGAGGA[A/G]TTGATTTAGGGGCAG | 284434 |
rs759376632 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16780017 | AGCTGGGCTTGCTCA[A/T]GTATCTGCAGTCAGT | 284434 |
rs759382643 | snp | C/T | 4.94482e-05 | 0.00497209 | utr-variant-3-prime, synonymous-codon | NWD1 | GRCh38.p7 | 19:16815059 | CCAGTTTGTCCATGC[C/T]GTGGTAAACAGAATC | 284434 |
rs759384631 | snp | A/G | 1.75705e-05 | 0.00296394 | intron-variant, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800177 | GGTTGGTAAGGTATA[A/G]GTATGGTCATTTTTG | 284434 |
rs759395387 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16792405 | AAATTGACCAGGCAC[A/G]GTGGCTCACACCTGT | 284434 |
rs759406447 | snp | C/T | 3.35999e-05 | 0.00409864 | intron-variant | NWD1 | GRCh38.p7 | 19:16791674 | TCAGCTTGAAAGTGC[C/T]CAGATGTGCTAGAAG | 284434 |
rs759429845 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16778974 | GAACAGCATCCCTGG[C/G]CTGCACCCACCAGAT | 284434 |
rs759446834 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16805121 | TGGAGTGCAGTGGCG[C/T]GATCTCAGTTCACTG | 284434 |
rs759471981 | in-del | -/AAAAAA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732654 | GCAAGACTTCATCTC[-/AAAAAA]AAAAAAAAAAAAAAA | 284434 |
rs759507440 | snp | C/G | 1.79393e-05 | 0.00299488 | missense | NWD1 | GRCh38.p7 | 19:16807625 | CCTCCAGTGAGATCA[C/G]GTGTCTGGAGGTTGC | 284434 |
rs759533828 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16760197 | ACTAAACTAAACTAA[A/G]CTAGGTGAAGTTCAT | 284434 |
rs759548962 | snp | C/T | 3.31857e-05 | 0.00407329 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749460 | AGTTTGTGGTGAGGG[C/T]CAATCACCAGGTCCT | 284434 |
rs759560513 | snp | A/G | | | utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16720202 | CTATGTGCCAGGCAC[A/G]CCAGCCTTACCAGAC | 284434 |
rs759605098 | snp | G/T | | | intron-variant, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800326 | ATCACCTGAGGTCAG[G/T]AGTTCAAGACCAGCC | 284434 |
rs759609414 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16786488 | TGTTAGCCCTTGACC[C/G]TCTTCCTCCTTCCCC | 284434 |
rs759622167 | snp | C/G | 1.73691e-05 | 0.00294691 | synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749725 | GCAGATGCCAAGGCT[C/G]CTGGGGCACAAGACA | 284434 |
rs759632082 | snp | C/T | 1.65195e-05 | 0.00287393 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16759300 | GGATGTGTACCGAGA[C/T]TGGACCCCGCCCAGC | 284434 |
rs759637150 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16812285 | CTGCACTCCAGCCTG[A/G]GTCAGACCTGTTAAA | 284434 |
rs759643635 | snp | A/G | 0.000163039 | 0.00902734 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744682 | CGGAGGCTGGGGCTC[A/G]TCACCCAGGAGCAGT | 284434 |
rs759709330 | snp | C/G | 6.59087e-05 | 0.00574021 | missense | NWD1 | GRCh38.p7 | 19:16779414 | GATGGCATCATGGCT[C/G]TGTGGGACATGGAAG | 284434 |
rs759713624 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16798193 | TTTAAGTTCAAAGTT[G/T]TCCAAGCTGGAGAGA | 284434 |
rs759747477 | snp | A/G | 1.73543e-05 | 0.00294565 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749790 | TGAGCTCAGATGCCC[A/G]TGGCCTGCTGAAGAG | 284434 |
rs759790863 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16810029 | CACAGTGAGCTCTGT[C/G]TGGGCAAAAGGATTT | 284434 |
rs759798259 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16763059 | CACTGAGATTACAGG[C/T]GTGTAATTACAGGTG | 284434 |
rs759816296 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16810993 | ACCTCAGCCTCCTAA[C/G]TAGCTGGGACTACAG | 284434 |
rs759818736 | snp | A/T | 1.65026e-05 | 0.00287246 | missense | NWD1 | GRCh38.p7 | 19:16791393 | AGCCGGTATTCCATA[A/T]CCTGGGAGATGCCTC | 284434 |
rs759854499 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16736277 | CTCTGCTGTCCAGGC[C/T]GGCATGCAGTAGTAC | 284434 |
rs759856482 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16722657 | CACACATTAAAGCTG[C/T]AGCTCTTGACCTGCT | 284434 |
rs759856542 | in-del | -/TTTTTTG | | | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718688 | CCAGCTAATTTTTTG[-/TTTTTTG]TTTTTTGTTTTTTGT | 284434 |
rs759868052 | snp | G/T | 1.64985e-05 | 0.0028721 | missense | NWD1 | GRCh38.p7 | 19:16765096 | GACCTGCTGGATGAC[G/T]TTGACCTGTGTGCCC | 284434 |
rs759894842 | snp | C/T | 0.000132186 | 0.00812867 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807779 | GTCCCTGAGCAAGTG[C/T]GAGGACCGCCTGGCC | 284434 |
rs759896281 | snp | A/G | 1.72707e-05 | 0.00293855 | intron-variant | NWD1 | GRCh38.p7 | 19:16814984 | TAGGATTGGACCTCT[A/G]CACCCCATTTTTCTC | 284434 |
rs759898508 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16767295 | TGCATGGCAGCAGGC[A/G]AGAGAGAGGGAGCAA | 284434 |
rs759979878 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16761798 | AGGAAAGTAAATTGA[C/T]GTAAGGAAAAAAAAA | 284434 |
rs759985288 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16767575 | ACCAGAAATCCCACC[A/G]TGCACTCCAGCCTGG | 284434 |
rs760015785 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16734930 | TTGCTTTTTTATTTC[G/T]TAATTTTTATTTTTT | 284434 |
rs760063591 | in-del | -/CA | 1.6477e-05 | 0.00287024 | frameshift-variant | NWD1 | GRCh38.p7 | 19:16779381 | TGGAGGAGAAGCTGC[-/CA]TGGTGATTGGCACCC | 284434 |
rs760074613 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16784082 | TGGTGGTGCACACCT[A/G]TAGTCCTAGCTACTT | 284434 |
rs760092881 | snp | G/T | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815496 | TCCATTATTCTTTCC[G/T]CTTTTTCATTTTCAT | 284434 |
rs760122543 | snp | C/G | 1.68052e-05 | 0.00289867 | missense | NWD1 | GRCh38.p7 | 19:16765177 | TGCCGCCCTGCTGTG[C/G]AGCTCCGAGGCATGG | 284434 |
rs760124266 | in-del | -/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787304 | GCTAATTATTTTTTT[-/G]CAAGATTATAAAAAT | 284434 |
rs760148607 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16770230 | AGGTGGAGATAATCG[A/C]ATCATGGAGGTGTTT | 284434 |
rs760192740 | snp | A/G | 1.68218e-05 | 0.00290011 | missense | NWD1 | GRCh38.p7 | 19:16750228 | GGGCCAGCCTCCCAG[A/G]GTGTGGGAACCCAGG | 284434 |
rs760210161 | in-del | -/ATA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790816 | TAGGTTGAATAAAAT[-/ATA]ATACTAAAATTGATT | 284434 |
rs760224202 | snp | C/T | 5.50716e-05 | 0.00524717 | intron-variant | NWD1 | GRCh38.p7 | 19:16765228 | TAGGAGTGACCAGGA[C/T]GGGCACTGACTTCTA | 284434 |
rs760227295 | in-del | -/GCAT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764378 | CATCCATCCATCCAT[-/GCAT]CCATCCATCCATCCA | 284434 |
rs760255405 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16737074 | ATAGAACTTTGGGAT[C/T]CTGGAAAGCCATGGA | 284434 |
rs760257470 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782775 | GGATGCCTTGAGCCC[A/G]GGTGTTTGAGTTCAG | 284434 |
rs760273866 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16814243 | CTCCCATTTACAGAG[C/T]AAAAACTGAGGCTCT | 284434 |
rs760300236 | in-del | -/GATA | 3.41146e-05 | 0.0041299 | intron-variant | NWD1 | GRCh38.p7 | 19:16808188 | AGGCATTGGAAAACT[-/GATA]GATAGCCATCATTTA | 284434 |
rs760317350 | snp | G/T | 1.65872e-05 | 0.00287981 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749453 | GGTGAGCAGTTTGTG[G/T]TGAGGGCCAATCACC | 284434 |
rs760334940 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16723410 | CACCATGTTGCCCAG[G/T]CTGGTCTTGAACCCT | 284434 |
rs760349128 | snp | C/T | 1.6525e-05 | 0.00287441 | missense | NWD1 | GRCh38.p7 | 19:16773140 | GAGAGGAGCCTCCTG[C/T]ACACAGAACTGCTGG | 284434 |
rs760404247 | snp | A/G | 0.00172438 | 0.0293124 | synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744528 | GCCAAGTGACCTGGA[A/G]CTGGTGGCACGATAC | 284434 |
rs760463280 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16802005 | AAAATAAAAATAATG[A/G]CCGGGCATGGTGGCT | 284434 |
rs760472146 | snp | G/T | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748835 | TCTCAATAATAATAA[G/T]AATAAGAAGAAGAAT | 284434 |
rs760472411 | snp | A/G | | | utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16720180 | ATGATAATTTACTGA[A/G]CACCTACTATGTGCC | 284434 |
rs760502887 | snp | C/T | 1.64773e-05 | 0.00287026 | missense | NWD1 | GRCh38.p7 | 19:16779382 | TGGAGGAGAAGCTGC[C/T]GGTGATTGGCACCCA | 284434 |
rs760506784 | in-del | -/TTCCTTCCTTCT/TTCT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16736197 | TCTTTCCTTCTTTCC[-/TTCCTTCCTTCT/TTCT]TTCCTTCCTTCTTTC | 284434 |
rs760513839 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16776627 | TCACACAATGAGTGC[A/G]TAAGAAAAAAAGTAA | 284434 |
rs760526165 | snp | C/T | 0.000494063 | 0.0157095 | intron-variant, synonymous-codon | NWD1 | GRCh38.p7 | 19:16812798 | CAAGGATGACAAGTA[C/T]GTGTACGTGGGCTTA | 284434 |
rs760546694 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16803991 | TATACATTTTCTGCA[G/T]GAGGTAGTTGGCAAT | 284434 |
rs760570640 | snp | A/C/T | 5.42464e-05 | 0.00520776 | intron-variant | NWD1 | GRCh38.p7 | 19:16762154 | GTGAGGTACCTGGGA[A/C/T]CCCCATTCCCCACCT | 284434 |
rs760617643 | snp | C/T | 0.000214431 | 0.0103523 | synonymous-codon, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800080 | CCGCACCGGCCTCAC[C/T]GCAGTGTCCCACAAT | 284434 |
rs760631692 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732054 | AAACTCTGTCTCTAC[C/T]AAAAATATAAAAATT | 284434 |
rs760650836 | snp | C/G | 3.30006e-05 | 0.00406192 | intron-variant | NWD1 | GRCh38.p7 | 19:16812897 | GCTTCGATCTGGAGA[C/G]AAAAGGCTCTGACCT | 284434 |
rs760667879 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16771040 | TGCGGGGGTTCACGC[C/T]TCTAATCCCAGCACT | 284434 |
rs760712988 | snp | A/C | 1.65597e-05 | 0.00287743 | missense | NWD1 | GRCh38.p7 | 19:16807756 | GCCCGGAAAGCAATC[A/C]ACTGCATGTCCCTGA | 284434 |
rs760794744 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16810830 | ACTATTAATTAAACT[A/G]TCAACCTTATGGGAA | 284434 |
rs760800433 | snp | A/G | 3.66905e-05 | 0.00428298 | missense | NWD1 | GRCh38.p7 | 19:16750398 | CACGTGCTGGGCTAC[A/G]TTGTGTCTTCCCGGT | 284434 |
rs760804581 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16797906 | GGGGAGATCTGGGAC[C/T]CTTCATCCTCACCTC | 284434 |
rs760809412 | snp | C/T | 2.13769e-05 | 0.00326925 | intron-variant | NWD1 | GRCh38.p7 | 19:16773355 | TAGCAAAAATCCCAG[C/T]AGGCACCTGCTTGCC | 284434 |
rs760828435 | snp | C/G | 1.64928e-05 | 0.00287161 | missense | NWD1 | GRCh38.p7 | 19:16765083 | TGGGGGCATTGAAGA[C/G]CTGCTGGATGACTTT | 284434 |
rs760834194 | snp | A/G | 1.7386e-05 | 0.00294834 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749708 | ATGTGCAAGCTGGCT[A/G]AGCAGATGCCAAGGC | 284434 |
rs760835738 | snp | A/G | 3.39916e-05 | 0.00412246 | intron-variant | NWD1 | GRCh38.p7 | 19:16797715 | GAGAGGTGTAACCCC[A/G]GTTCCTGCCGTTTCA | 284434 |
rs760847660 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16809852 | ATGAGCCACCGTGCC[A/T]GGCTGCTCCGTGCTA | 284434 |
rs760855501 | snp | A/G | 1.69487e-05 | 0.00291103 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749627 | CAGCAGCTCAGGCAC[A/G]ATGACAGCAAGCAGC | 284434 |
rs760871205 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16779813 | AGCTAATTTTTTAAT[G/T]TTTTTAGAAATGGGG | 284434 |
rs760930370 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16810091 | CCTTGTTCCTAGGAG[-/A]AACTCCTGACATTTC | 284434 |
rs760960238 | snp | A/C/G | 3.35167e-05 | 0.00409358 | missense | NWD1 | GRCh38.p7 | 19:16750011 | CCCTGGCTGCCTCTC[A/C/G]ACTGCCCCCCGAGGG | 284434 |
rs761023980 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16738203 | TGTAAAGCCAAAAGT[A/G]TTGACTGTCTGACTT | 284434 |
rs761041065 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16770734 | AACCTCCACCCGTGT[C/T]GCCATCGAGGGTCCT | 284434 |
rs761083141 | snp | C/T | 1.6681e-05 | 0.00288794 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750059 | GCTTGCTCGGGGGCA[C/T]TGGGGGTTTTGGACA | 284434 |
rs761103233 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16798959 | AAAAAAAAACATTAA[A/C]AGTTTTGAGCTTCCA | 284434 |
rs761113256 | snp | A/G | 1.64751e-05 | 0.00287007 | missense | NWD1 | GRCh38.p7 | 19:16789089 | GGCCAGGAGAAATTT[A/G]CCATTTGGGATGGAG | 284434 |
rs761137837 | in-del | -/TT | 1.64781e-05 | 0.00287033 | frameshift-variant | NWD1 | GRCh38.p7 | 19:16779370 | GGCATGGGGTGTGGA[-/TT]GGAGAAGCTGCTGGT | 284434 |
rs761146492 | in-del | -/AAAAC/AAAAGAAAAC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16737980 | AAAAGAAAAGAAAAG[-/AAAAC/AAAAGAAAAC]AAAAGAAAAGAAAAG | 284434 |
rs761150008 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16772930 | GCTGGAGACTGGAAA[C/G]AGCTGGGTGCCTCTG | 284434 |
rs761156096 | in-del | -/TCCA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754628 | CCATCATCTCTATCT[-/TCCA]TCCATCCATCCATCC | 284434 |
rs761217379 | snp | C/G | 5.49083e-05 | 0.00523939 | intron-variant | NWD1 | GRCh38.p7 | 19:16789209 | ACAAACATATGCCCT[C/G]TTTGTAAAGGAAAGC | 284434 |
rs761272591 | snp | C/G | 1.67964e-05 | 0.00289792 | intron-variant | NWD1 | GRCh38.p7 | 19:16765002 | GGAGGGAGGTAGGCA[C/G]TTCCCACATCCTCCC | 284434 |
rs761277348 | snp | C/T | 1.64928e-05 | 0.00287161 | missense, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800070 | CATTTCTGGACCGCA[C/T]CGGCCTCACCGCAGT | 284434 |
rs761279336 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16781449 | GGTGAACCCACATCT[C/T]TACAAAAAATGCAAA | 284434 |
rs761304192 | snp | A/T | 1.68055e-05 | 0.0028987 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815341 | GTAAAAAAATAAAAA[A/T]AAAAAAACCCTGTGG | 284434 |
rs761314570 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16755775 | ACTCCTGGGCTCAAG[C/T]GATCCTCCCACCTTG | 284434 |
rs761318548 | in-del | -/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16798275 | AAGTTCTCTTTTTTT[-/C]CCCCCTCCTTCTTAT | 284434 |
rs761324687 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16742087 | GTGTCTCAAAAAAAG[C/T]AAATAGGCCAGGCGC | 284434 |
rs761334419 | in-del | -/GAGTACTTTG | 1.64768e-05 | 0.00287021 | frameshift-variant | NWD1 | GRCh38.p7 | 19:16808030 | CCGAGTTGCCTGTGT[-/GAGTACTTTG]GGAGGTCAGCCACAA | 284434 |
rs761335866 | in-del | -/CTT | 4.9516e-05 | 0.00497549 | cds-indel | NWD1 | GRCh38.p7 | 19:16762054 | TGGCGTCCTGGCCGA[-/CTT]CTTCTCAGGGACCTG | 284434 |
rs761336469 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16794328 | CCAAGATCATACCAC[C/T]GCACTCCTGCCTGGG | 284434 |
rs761346051 | snp | C/T | 1.78583e-05 | 0.00298811 | intron-variant | NWD1 | GRCh38.p7 | 19:16762147 | CCGAAAGGTGAGGTA[C/T]CTGGGACCCCCATTC | 284434 |
rs761386610 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16721050 | GATGGGGTTTCGCCA[-/T]TGTTGGCCAGGCTGG | 284434 |
rs761394264 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751039 | CCAGCCTGACAAAAC[A/G]TGGAGAAACTCTGTC | 284434 |
rs761403351 | snp | C/T | 4.94303e-05 | 0.00497119 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16791430 | TTGGATGTGCATGGC[C/T]GTGCTGGCCTCCCAG | 284434 |
rs761456386 | snp | A/G | 1.64798e-05 | 0.00287047 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16791508 | CTCAGCTACGGGAAA[A/G]CTTCAGGGGAAGCAA | 284434 |
rs761500318 | snp | C/T | 8.28562e-05 | 0.00643593 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749376 | AGACCCACCGCCTGC[C/T]GTGGAGCCGCGACTT | 284434 |
rs761517752 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16797981 | AAATACAGACACCCA[C/G]AAAAATGAGTGCAGG | 284434 |
rs761529285 | snp | C/T | 0.000115574 | 0.00760088 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16765110 | CTTTGACCTGTGTGC[C/T]CCTCACCTGGACTCC | 284434 |
rs761617069 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16757966 | CTGAGGCAGGAGAAT[C/T]GCTTGAAGCCAGGAG | 284434 |
rs761628946 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16730316 | ACAGAGTAAGACTTC[A/G]TCTCAAAAAACAAAC | 284434 |
rs761629685 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16727814 | GCCTGTAATCCCAGC[A/G]CTTTGGGAGGCTGAG | 284434 |
rs761661878 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16788765 | ATTAGGCATACAAGC[A/G]TGAGAACTCTTTCTC | 284434 |
rs761665270 | snp | A/G | 0.000133147 | 0.00815817 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16736716 | TGGAGGAGGTTGACC[A/G]GTGTTGGAAAACATC | 284434 |
rs761682934 | snp | A/G | 1.64784e-05 | 0.00287035 | missense | NWD1 | GRCh38.p7 | 19:16779375 | TGGGGTGTGGAGGAG[A/G]AGCTGCTGGTGATTG | 284434 |
rs761697644 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16801934 | GCAGAAACAGGAAGA[C/T]TGCTTGAGGCCGGGA | 284434 |
rs761719874 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16743471 | CCTTGGCCTCCCAAA[G/T]TGTTGGGATTACAGG | 284434 |
rs761748904 | snp | A/G | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815408 | TAGTTAAAGCAAAAA[A/G]AATACGTTTGCTGGT | 284434 |
rs761751065 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16800662 | GTCTGGTGAGGACCC[A/G]TTTCCTGGTTCACAG | 284434 |
rs761762025 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16784200 | ACAGTGAGACTCAGT[C/G]TTAAAAAGAAAAAAA | 284434 |
rs761796201 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782644 | AAAATCAAAAGTTTA[A/G]TTGGCCCTCCATATC | 284434 |
rs761836311 | snp | A/T | 1.68917e-05 | 0.00290613 | intron-variant | NWD1 | GRCh38.p7 | 19:16764989 | CCCAGGATGAACTGG[A/T]GGGAGGTAGGCACTT | 284434 |
rs761840107 | in-del | -/TTTTTG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16809568 | CTTTTTCTTTTTTTT[-/TTTTTG]AGATGGAGTCTTGCT | 284434 |
rs761863491 | snp | G/T | 1.64746e-05 | 0.00287002 | utr-variant-3-prime, missense | NWD1 | GRCh38.p7 | 19:16815188 | TCTTAAGAACTTCAA[G/T]AAGGCAATGTGGATG | 284434 |
rs761871402 | snp | C/G | 3.3112e-05 | 0.00406877 | missense | NWD1 | GRCh38.p7 | 19:16762091 | CAGGGTACCAAGAAG[C/G]TCATCACTCTGCCAC | 284434 |
rs761881195 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16789997 | TGCTGGGATTACAGG[C/G]CTGAGCCATCATGCC | 284434 |
rs761897363 | snp | C/T | 3.36214e-05 | 0.00409995 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807695 | GGTCGTCCTTGTGTT[C/T]CCCCTGAATTCCAGG | 284434 |
rs761967495 | snp | C/T | 1.76312e-05 | 0.00296906 | intron-variant | NWD1 | GRCh38.p7 | 19:16789199 | CTCAAAGGTAACAAA[C/T]ATATGCCCTGTTTGT | 284434 |
rs761986164 | snp | C/T | 1.97276e-05 | 0.0031406 | utr-variant-3-prime, missense | NWD1 | GRCh38.p7 | 19:16815315 | AAATGCTCACAAGTG[C/T]GCCTGATAGTGTAAA | 284434 |
rs762002039 | snp | C/T | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748654 | CATAGTAAGACCCCA[C/T]CTCTACAAAAAATAC | 284434 |
rs762009990 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16758762 | AGAGGAAAAGATTGG[C/G]ACTTTGGGAGACCGA | 284434 |
rs762020297 | snp | G/T | | | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744963 | CTTCTTGTCTCCCAG[G/T]GAGGTTCCTGGCACA | 284434 |
rs762064582 | in-del | -/G | 1.89712e-05 | 0.00307981 | frameshift-variant | NWD1 | GRCh38.p7 | 19:16759350 | GCCCCTGCTGTGGGT[-/G]GCGGCTTCGTCGGGA | 284434 |
rs762100853 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16789489 | TCCTGTAAATTTTGA[C/T]GTGTGTTTTCATTTA | 284434 |
rs762103487 | snp | A/G | 0.000106752 | 0.00730511 | intron-variant | NWD1 | GRCh38.p7 | 19:16759459 | AGTGGCAGCGACACT[A/G]TCTGGGTGGGACCCC | 284434 |
rs762104324 | in-del | -/TTCTT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16778492 | TTCTTCTTCTTCTTC[-/TTCTT]TTTTTTTTTTTTGTT | 284434 |
rs762108204 | in-del | -/T | 1.654e-05 | 0.00287571 | frameshift-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749313 | ATGCCCAGAACCTTC[-/T]CAGCAGCCTCAAAAG | 284434 |
rs762110086 | snp | C/G/T | 3.29527e-05 | 0.00405898 | missense | NWD1 | GRCh38.p7 | 19:16797789 | GCTTTCGCCGATTCA[C/G/T]GGCCATGGATCTGGA | 284434 |
rs762146683 | snp | C/T | 1.692e-05 | 0.00290856 | missense, intron-variant | NWD1 | GRCh38.p7 | 19:16749918 | CTCCACACTGTCTCT[C/T]GCAGAAACTTCGAGT | 284434 |
rs762161862 | snp | C/T | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748014 | TTTGAGATGGAGTCT[C/T]GCTCTGTTGCACAGG | 284434 |
rs762165038 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16810598 | CACAGCAAGATCCCA[C/T]CTCTAGAAAAAAAAA | 284434 |
rs762174953 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754612 | ATCTGTCTTCCTTTT[A/T]TCCATCATCTCTATC | 284434 |
rs762226680 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16797179 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 284434 |
rs762233189 | snp | C/T | 1.65181e-05 | 0.00287381 | missense, utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16797867 | TGATCATCACGGGGT[C/T]CCTTGATGCGCTCAT | 284434 |
rs762235126 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16785060 | AGACAAGAGGCAGAT[C/T]AGTGGTGGCCAGGGG | 284434 |
rs762324791 | snp | C/T | 0.000135547 | 0.00823136 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16736694 | CACTTGACCACAGAA[C/T]TCTGCTTGGAGGAGG | 284434 |
rs762354302 | in-del | -/GGA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16798145 | TTGTGCCTTCAGAGT[-/GGA]GGAGCAGGGTTGTGG | 284434 |
rs762357400 | snp | A/T | 0.000263848 | 0.0114828 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16762018 | GCGCTACCTGTCAGG[A/T]TCCGAGAGAGCCAAG | 284434 |
rs762359976 | snp | C/T | 7.30313e-05 | 0.00604238 | intron-variant | NWD1 | GRCh38.p7 | 19:16799836 | CGTATTTCTGAACTA[C/T]AGTTGTCCACAGAAG | 284434 |
rs762365765 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16813638 | CCCACCACCACACTC[A/T]GCTAATTTTTGTATT | 284434 |
rs762374318 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16725164 | GACTACAGGCGTGCA[C/T]CACCATGGCCAGCTA | 284434 |
rs762418805 | snp | C/T | 6.70264e-05 | 0.00578867 | missense | NWD1 | GRCh38.p7 | 19:16750017 | CTGCCTCTCAACTGC[C/T]CCCCGAGGGTGCACC | 284434 |
rs762430334 | snp | A/G | 4.95765e-05 | 0.00497853 | missense | NWD1 | GRCh38.p7 | 19:16808110 | GACCTGCAGGCACGC[A/G]AGTGGAAATTCGAGA | 284434 |
rs762478359 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16774558 | ATCCACCCATCCGTT[A/G]TTCATCGATTCATCA | 284434 |
rs762509381 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16720920 | CAGTGGCACGATCTC[A/G]GCTCACTGCAACCTC | 284434 |
rs762528247 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16760366 | TGGACTCAAGCAACC[C/G]TCCCACCTCAGCCTC | 284434 |
rs762537699 | snp | A/G | 1.81618e-05 | 0.0030134 | missense | NWD1 | GRCh38.p7 | 19:16773321 | TCAGCGGCTGTCACA[A/G]AGGTGAGTCTCCCCA | 284434 |
rs762556352 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16774136 | CCACCCTTCCATCCA[C/T]CTACTGCCCCATCCA | 284434 |
rs762564679 | snp | A/C/G | 3.30968e-05 | 0.00406786 | missense | NWD1 | GRCh38.p7 | 19:16762088 | AGCCAGGGTACCAAG[A/C/G]AGCTCATCACTCTGC | 284434 |
rs762609492 | snp | C/T | 4.94735e-05 | 0.00497336 | missense, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800066 | GCACCATTTCTGGAC[C/T]GCACCGGCCTCACCG | 284434 |
rs762640582 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16733372 | CTAAAAATACAAAAA[C/T]TACCCAGATGTGGTG | 284434 |
rs762665877 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16720319 | TGCAGAAAATTAAAA[C/T]AAGGCGATGGCATTG | 284434 |
rs762670129 | in-del | -/ACC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16807516 | AACAAAACAAAAAAA[-/ACC]ACCAGGGAAGCAGGG | 284434 |
rs762670499 | snp | A/C | 5.09567e-05 | 0.00504735 | missense | NWD1 | GRCh38.p7 | 19:16750309 | TGCCTGTCCCGCTGG[A/C]CACCACCGCAGAGGA | 284434 |
rs762685284 | snp | A/G | 2.12999e-05 | 0.00326336 | intron-variant | NWD1 | GRCh38.p7 | 19:16789241 | GAGACCAGAGCATTC[A/G]AAGACAGAATAGGCC | 284434 |
rs762685705 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16767539 | AAAATTGCTTGAACA[C/T]GGGCGGCAGAGGTTG | 284434 |
rs762699241 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16726816 | GGCTTCCTGGGCATT[C/G]TTAGATGTTGAGCAG | 284434 |
rs762733094 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16738125 | ACTTGTTTACACATT[C/G]TTTAGCCCTGCTTTC | 284434 |
rs762781688 | snp | A/G | 1.70171e-05 | 0.00291689 | missense | NWD1 | GRCh38.p7 | 19:16807681 | GGCCTCGTGTCGGGG[A/G]TCGTCCTTGTGTTCC | 284434 |
rs762783489 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16768474 | TGGAAATTTTGTGTT[C/T]AACTTTTTGAGGAAC | 284434 |
rs762791656 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16799384 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 284434 |
rs762795550 | snp | C/T | 1.79712e-05 | 0.00299755 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750382 | GCAGCTCCTCGTGGC[C/T]CACGTGCTGGGCTAC | 284434 |
rs762814388 | snp | A/T | 2.85784e-05 | 0.00378 | intron-variant | NWD1 | GRCh38.p7 | 19:16794422 | GACTTGTAACCCTTA[A/T]CCCGTGGAAGTGCCT | 284434 |
rs762821990 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16794103 | AGGCATGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 284434 |
rs762824998 | in-del | -/CT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16784756 | CAACATGGTGAACCC[-/CT]GTCTCTACTAAAAAT | 284434 |
rs762826355 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16813443 | TTCATTCTTTGCCCC[C/T]GCCTTATAGATGTTA | 284434 |
rs762835725 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16750915 | GCCTAGTAAAAGTCT[C/T]GGAGCTATAAATTGC | 284434 |
rs762858548 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16742045 | GATTGTACCACTGCA[C/T]GCCAGCCTGGGTGAC | 284434 |
rs762876450 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16735195 | GCACAACCAACTATG[C/T]TGTTACAACTATGAA | 284434 |
rs762878889 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16812406 | AGGCACGTTGGCTCA[C/T]ACCTGTAATCCCAGC | 284434 |
rs762891924 | in-del | -/CCAT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764470 | GCTGGTTATAACCAT[-/CCAT]CCATCCATCCATCCA | 284434 |
rs762938287 | snp | C/T | 2.58535e-05 | 0.00359529 | missense, intron-variant | NWD1 | GRCh38.p7 | 19:16794539 | TCTCTGAAGATGAGT[C/T]CCTCCTCGCCGCAGG | 284434 |
rs762966540 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16746093 | GGTGTGGTGGCTCAT[A/G]CCTGTAATCCCAGCA | 284434 |
rs763016140 | snp | C/T | 4.94262e-05 | 0.00497098 | utr-variant-3-prime, missense | NWD1 | GRCh38.p7 | 19:16815097 | CCACCAGTGGCTTCA[C/T]TGCCCCCACCAGGCA | 284434 |
rs763053865 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16789493 | GTAAATTTTGACGTG[G/T]GTTTTCATTTACATT | 284434 |
rs763068932 | snp | C/T | 0.000162959 | 0.00902514 | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744748 | ACTCCCCTCTGGAGA[C/T]CCACAAGAAACTGAC | 284434 |
rs763086350 | snp | A/G | 1.65647e-05 | 0.00287786 | intron-variant | NWD1 | GRCh38.p7 | 19:16779502 | TTGTGGTCAGCTTCC[A/G]TAGTGAAAAGTTGGT | 284434 |
rs763135893 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16757775 | TAGAATTTTGCAGGC[C/T]AGGTGCAGTGGCTCA | 284434 |
rs763146697 | snp | A/G | 5.36956e-05 | 0.00518121 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807632 | TGAGATCAGGTGTCT[A/G]GAGGTTGCTGAGCAG | 284434 |
rs763177291 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16753766 | GAAACCTTGCCTTAG[C/T]CTGAGAGACCCTATC | 284434 |
rs763181661 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16724217 | CACTAATGCTGGGCA[C/T]TTTATAGACCTATCT | 284434 |
rs763214334 | snp | A/G | 3.38203e-05 | 0.00411206 | missense | NWD1 | GRCh38.p7 | 19:16765184 | CTGCTGTGGAGCTCC[A/G]AGGCATGGGTGAGTC | 284434 |
rs763225891 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16783170 | CTGAAGAGCTAGGAG[C/T]ACAGGTGCATGCCAC | 284434 |
rs763228474 | in-del | -/CCTTCCCA | 5.42059e-05 | 0.00520577 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749113 | ATAATGACCACACTT[-/CCTTCCCA]CCTTCCCCACTTTGG | 284434 |
rs763260961 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16809559 | TTCTTTTTCTTTTTC[-/T]TTTTTTTTTTTTTGA | 284434 |
rs763266746 | snp | C/G | 1.65644e-05 | 0.00287783 | missense | NWD1 | GRCh38.p7 | 19:16759311 | GAGATTGGACCCCGC[C/G]CAGCAAGGAGCTGCT | 284434 |
rs763290772 | snp | A/G | 9.88386e-05 | 0.00702919 | utr-variant-3-prime, synonymous-codon | NWD1 | GRCh38.p7 | 19:16815164 | AGCAAAAGCCTCACC[A/G]CAGGACCCTCTTAAG | 284434 |
rs763311682 | snp | C/T | 3.29766e-05 | 0.00406045 | missense | NWD1 | GRCh38.p7 | 19:16763855 | CCTCTGTGGTTCTCA[C/T]ATACGGTTGCAAACC | 284434 |
rs763433638 | in-del | -/GA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764955 | GCCCTGGAGGAAATG[-/GA]GAGATGATTCTCCAC | 284434 |
rs763456988 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16795730 | CCTAATTTGCTCTTT[C/T]AGTTCCACCATCTGC | 284434 |
rs763488972 | in-del | -/TATTATTATTAT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16742882 | TCTCACTATGTTGCC[-/TATTATTATTAT]TATTATTATTATTAT | 284434 |
rs763496114 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732596 | CCAATCCCTGGCTAG[A/G]GAATTTTTTTTTTTT | 284434 |
rs763509072 | in-del | -/GTTT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16723713 | GTTTTGTTTTGTTTT[-/GTTT]TGAGATGGACTGTCC | 284434 |
rs763513364 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16721008 | GGTACATGCCACCGC[A/G]CCAGCTAATTTTTGT | 284434 |
rs763537081 | snp | C/T | 4.88866e-05 | 0.00494378 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16759402 | GCGGCCCGTGGATGG[C/T]TTCACCCTCCTGGCC | 284434 |
rs763566625 | in-del | -/TG | 6.59114e-05 | 0.00574033 | frameshift-variant | NWD1 | GRCh38.p7 | 19:16779409 | CCCAGGATGGCATCA[-/TG]GCTGTGTGGGACATG | 284434 |
rs763587449 | snp | C/T | | | synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749809 | CCTGCTGAAGAGCAT[C/T]TGCTTCCAGGTGTGC | 284434 |
rs763600229 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16733392 | CAGATGTGGTGACAC[A/G]CACCTGTAATCCCAG | 284434 |
rs763603072 | snp | A/G | 3.30033e-05 | 0.00406209 | synonymous-codon, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16799981 | CGGGGCTTTGGTGGC[A/G]TCTGCTTCCCCACAG | 284434 |
rs763604438 | snp | A/G | 0.0001 | 0.00707036 | missense | NWD1 | GRCh38.p7 | 19:16750074 | CTGGGGGTTTTGGAC[A/G]CCTTGCAGCGGGTGC | 284434 |
rs763610092 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16760537 | AGTGCTGGGATTACA[G/T]GTGTGAGCTACCATG | 284434 |
rs763622229 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16728888 | GGCGGAGCTTGCAGC[G/T]AGCCGAGATCATGCC | 284434 |
rs763627022 | in-del | -/G | 1.65499e-05 | 0.00287657 | frameshift-variant | NWD1 | GRCh38.p7 | 19:16762090 | CCAGGGTACCAAGAA[-/G]CTCATCACTCTGCCA | 284434 |
rs763641040 | snp | C/T | 1.6736e-05 | 0.0028927 | intron-variant | NWD1 | GRCh38.p7 | 19:16791304 | CGGGAAACTTGTAGT[C/T]TAGGTCTCCTGCCAA | 284434 |
rs763651617 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16750922 | AAAAGTCTCGGAGCT[A/G]TAAATTGCAATAAAC | 284434 |
rs763679331 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16728943 | GCATGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 284434 |
rs763689190 | snp | C/T | 4.94866e-05 | 0.00497402 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749227 | AGAGATCCAAGACCT[C/T]CACAAACACATCCTT | 284434 |
rs763696152 | snp | A/C | 5.00279e-05 | 0.00500115 | intron-variant | NWD1 | GRCh38.p7 | 19:16765015 | CACTTCCCACATCCT[A/C]CCCCCTTCTCTCCCT | 284434 |
rs763707450 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16805441 | TCAAGCAATCTGCCT[A/G]CCTCAGCCTCCCAAA | 284434 |
rs763709491 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16791730 | TCTTTGTTTTGTTTT[C/G]GAGATGAAGTTTCAC | 284434 |
rs763734983 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16799488 | TGTGAGCCACTGCAC[C/T]TGGCCTATTTATTTA | 284434 |
rs763766726 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16734184 | CTTTGCAAGGAAAGC[G/T]TTGTGAACAAGTGTG | 284434 |
rs763817572 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16756303 | TACTATTCATGAAGT[A/G]GAAGTGGATATCACA | 284434 |
rs763818975 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16793023 | GCACTCCAGCCTGAG[C/T]GACAGAGCCAGGCCC | 284434 |
rs763850980 | snp | C/T | 1.64909e-05 | 0.00287144 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16791403 | CCATATCCTGGGAGA[C/T]GCCTCTGATCCTTGG | 284434 |
rs763851471 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16772564 | GGCAGGAGAATCGCT[C/T]GAACCTGGGAGGTGC | 284434 |
rs763885045 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16726905 | AGGTCTCCAGACATT[C/G]CAAGTGTCCCCTGGG | 284434 |
rs763927023 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16813572 | GTCTCTGCCTCCCAG[A/G]TTCAAGTGATTCTCC | 284434 |
rs763934879 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751175 | GTTGCCGTGAGCCGA[A/G]ATCACGCCATTGCAC | 284434 |
rs763964096 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16757067 | TCTACATGATGGGGA[A/G]TTGTAGAATTATTTC | 284434 |
rs763983237 | snp | C/G | 3.35751e-05 | 0.00409712 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749604 | AGGAACTCCTGGCCC[C/G]GCTTGGGCAGCAGCT | 284434 |
rs763989600 | snp | G/T | 1.64765e-05 | 0.00287019 | missense | NWD1 | GRCh38.p7 | 19:16808026 | AGGAGCCGAGTTGCC[G/T]GTGTGGAGGTCAGCC | 284434 |
rs764013265 | snp | A/T | 1.65282e-05 | 0.00287469 | missense | NWD1 | GRCh38.p7 | 19:16773179 | CATTTCTTCGCCACC[A/T]CACATCCAGCACTGG | 284434 |
rs764021102 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16756084 | GAGAAAAGAAAATGA[C/T]AGTAAGAAAATCATA | 284434 |
rs764038027 | snp | C/T | 1.66413e-05 | 0.0028845 | intron-variant | NWD1 | GRCh38.p7 | 19:16815025 | TTCTCTTCACCCTTA[C/T]AGGCACCCTGCTGAC | 284434 |
rs764040948 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16767540 | AAATTGCTTGAACAC[A/G]GGCGGCAGAGGTTGC | 284434 |
rs764065279 | in-del | -/TTTTTTTT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16783003 | CTCCTTTCTCTCTCT[-/TTTTTTTT]CTTTCTTTCTTTCCT | 284434 |
rs764106454 | snp | A/G | 0.000403741 | 0.0142024 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16736703 | ACAGAACTCTGCTTG[A/G]AGGAGGTTGACCGGT | 284434 |
rs764121136 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16812421 | CACCTGTAATCCCAG[A/C]ACTTTGCGAGACCAA | 284434 |
rs764129661 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16722010 | TCCAGCTACTTGAGA[C/T]GCCGAGGCAGGAGGA | 284434 |
rs764158829 | snp | A/T | 1.64917e-05 | 0.00287151 | missense | NWD1 | GRCh38.p7 | 19:16762019 | CGCTACCTGTCAGGA[A/T]CCGAGAGAGCCAAGA | 284434 |
rs764164715 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16807383 | TTGTAATCCCAGCTA[C/T]TCGGGAGGCTGCGGC | 284434 |
rs764224678 | in-del | -/ACC | 1.68103e-05 | 0.00289911 | cds-indel, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749181 | TGCTGAGCTCAGAGG[-/ACC]GGGAACAGGGAGCCA | 284434 |
rs764234229 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16722716 | ATGGGATAAGGGTGT[A/C]TTTGTTTACCTGGAG | 284434 |
rs764250635 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16735215 | ACAACTATGAAATGA[A/G]CTTTGAGGACAGGTG | 284434 |
rs764259138 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16786730 | TTTCGTATTTTTAGT[A/G]GAGACGGGGTTTTGC | 284434 |
rs764320404 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16812925 | CCTGGGTCCTGGGCA[C/T]TAGAGGGCCCTGCTC | 284434 |
rs764342241 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16746845 | TAAACATAAGTGGAT[C/T]ATCAGTCACAAAGGT | 284434 |
rs764375391 | snp | A/G | 1.78921e-05 | 0.00299094 | missense | NWD1 | GRCh38.p7 | 19:16807634 | AGATCAGGTGTCTGG[A/G]GGTTGCTGAGCAGCG | 284434 |
rs764412072 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16800561 | AATAAATTATCCCCA[C/T]AGACTGGGTGGCATA | 284434 |
rs764425278 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16726719 | CTGGGATTATAGGTG[-/T]TGAGCCACTGCACCT | 284434 |
rs764462891 | snp | C/T | 2.8562e-05 | 0.00377892 | intron-variant | NWD1 | GRCh38.p7 | 19:16794423 | ACTTGTAACCCTTAA[C/T]CCGTGGAAGTGCCTG | 284434 |
rs764467941 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16752886 | CACCTGTAGTCCCAG[C/G]TACTCGGGAGGCTGA | 284434 |
rs764495804 | snp | A/G/T | 3.38199e-05 | 0.00411206 | missense | NWD1 | GRCh38.p7 | 19:16759329 | GCAAGGAGCTGCTGC[A/G/T]CTTCCCGCCCCTGCT | 284434 |
rs764529017 | snp | A/G | | | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807923 | CGTGGCCATTCTGAC[A/G]GACTACCGCGTGGTC | 284434 |
rs764535317 | in-del | -/C | 1.81566e-05 | 0.00301296 | intron-variant | NWD1 | GRCh38.p7 | 19:16807577 | ATTCTCATTTTTCTT[-/C]CCTGGCAGGCGAGGA | 284434 |
rs764547393 | snp | C/T | 1.65776e-05 | 0.00287898 | intron-variant | NWD1 | GRCh38.p7 | 19:16779506 | GGTCAGCTTCCATAG[C/T]GAAAAGTTGGTTCTC | 284434 |
rs764561704 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16723541 | CTGGTCTTGAACTCC[C/T]GGGCTCAAGCAATCC | 284434 |
rs764567397 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16753788 | GACCCTATCCATTCA[C/T]CCATCCATCAATCCC | 284434 |
rs764583758 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16810106 | GAACTCCTGACATTT[C/T]CTTGATGCTCAATAA | 284434 |
rs764596993 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16763196 | GCCTCTCCAGGACAT[A/G]GTCTGAGCCCCTTTC | 284434 |
rs764614448 | snp | C/T | 1.73243e-05 | 0.0029431 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749813 | CTGAAGAGCATCTGC[C/T]TCCAGGTGTGCCTGG | 284434 |
rs764615795 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16783174 | AGAGCTAGGAGCACA[A/G]GTGCATGCCACCATG | 284434 |
rs764632379 | in-del | -/AACA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16802282 | GTCTCAAAAATAAAT[-/AACA]AAATAAATAAAAATA | 284434 |
rs764654095 | in-del | -/AG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16765523 | ATTTTTCGTAGAGAC[-/AG]GGTCTCACTGTGTTG | 284434 |
rs764666356 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16803521 | GACAGGCCCAAGCTC[C/T]TGATACCATTCCACA | 284434 |
rs764692191 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16759179 | GCATCCTCCAAATGC[A/G]GAAGACATGAGATGT | 284434 |
rs764702085 | snp | C/G | 0.000163519 | 0.00904062 | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744759 | GAGACCCACAAGAAA[C/G]TGACCACGTGTTCAG | 284434 |
rs764711190 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16739358 | AAAAAAAAAAAAATT[A/T]TTTTTTTAAGGAAGA | 284434 |
rs764713175 | snp | C/T | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748928 | GTTGCAAATGCAAAC[C/T]CCGGGGCCCCACTCA | 284434 |
rs764732783 | snp | C/T | 1.64914e-05 | 0.00287149 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16762009 | GGTCCGTGAGCGCTA[C/T]CTGTCAGGATCCGAG | 284434 |
rs764751170 | snp | C/T | | | synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744708 | GCAGTGGCAGCACTA[C/T]CACCGGTCAGGTGAG | 284434 |
rs764794307 | snp | C/G | 5.41023e-05 | 0.00520079 | intron-variant | NWD1 | GRCh38.p7 | 19:16799871 | CAGATCTGCCCTCCT[C/G]TTCTGCTTCCTCAGG | 284434 |
rs764803317 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16733875 | CCTGCTCCTCTAACT[A/C]ATTGTTCCTCCCCCT | 284434 |
rs764809637 | snp | G/T | 1.6896e-05 | 0.0029065 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749933 | TGCAGAAACTTCGAG[G/T]CTCTCGTGCTCCTGC | 284434 |
rs764826773 | snp | A/G | | | utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16720205 | TGTGCCAGGCACGCC[A/G]GCCTTACCAGACAAG | 284434 |
rs764836395 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16797329 | GTTCCAAAACATCTC[-/T]TTTTTTTTTTTTTTT | 284434 |
rs764847216 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732457 | CTTCAGGAGGAGTAT[A/G]AGAGGGCTTTGCGAT | 284434 |
rs764849466 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16789091 | CCAGGAGAAATTTAC[C/T]ATTTGGGATGGAGGC | 284434 |
rs764864876 | snp | A/G | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817746 | CTGAAAAAATTAGCT[A/G]CTCTTTGCCACTGCT | 284434 |
rs764890433 | snp | C/G | 1.64779e-05 | 0.00287031 | utr-variant-3-prime, missense | NWD1 | GRCh38.p7 | 19:16815077 | GGTAAACAGAATCAT[C/G]CCAACCACCAGTGGC | 284434 |
rs764892546 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16796681 | TCATTTCTCTCCTTC[C/T]TCCCTTCCTCTTTAC | 284434 |
rs764914103 | snp | A/G | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815756 | TACTCCTGAGATGCA[A/G]ACTGGAGTTCTGGTA | 284434 |
rs764990072 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16784413 | AAAGTATACAGGAGG[A/T]TATATATAGGCTATA | 284434 |
rs765011725 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16780020 | TGGGCTTGCTCATGT[A/G]TCTGCAGTCAGTCAG | 284434 |
rs765016088 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16781799 | AATTAGCTTTAGAAA[G/T]AATCTAATCTAGGCC | 284434 |
rs765034013 | snp | A/G | 1.65883e-05 | 0.00287991 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749462 | TTTGTGGTGAGGGCC[A/G]ATCACCAGGTCCTCA | 284434 |
rs765077624 | in-del | -/CTCC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764400 | TCCATCCATCCATCC[-/CTCC]ATCTAACTATCCATT | 284434 |
rs765090731 | snp | C/T | | | stop-gained, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749570 | AGCTCGGAGGTCATT[C/T]AGACCTTCTGCGGAC | 284434 |
rs765130872 | snp | A/G | 1.65285e-05 | 0.00287471 | missense | NWD1 | GRCh38.p7 | 19:16791569 | ACCTGTGCCGTCTCA[A/G]TCCAGAAGCAAGGAA | 284434 |
rs765201936 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16779061 | GAAACCGATATGTGT[C/T]CGCTGGGTGAGCACT | 284434 |
rs765205938 | snp | A/T | 0.000148115 | 0.0086044 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744545 | TGGTGGCACGATACT[A/T]CCAGAGGGACGAGAA | 284434 |
rs765246509 | snp | A/G | 8.23608e-05 | 0.00641667 | intron-variant, missense | NWD1 | GRCh38.p7 | 19:16812808 | AAGTATGTGTACGTG[A/G]GCTTAAAGGATCGCT | 284434 |
rs765303589 | in-del | -/TTT/TTTTTTTTTT | | | downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16818417 | TAATATTTTGTTATC[-/TTT/TTTTTTTTTT]TTTTTTTTTTTTTTT | 284434 |
rs765331759 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16752117 | CAGAGACGCCAAGGA[A/G]CAAAACTTTGCCTTT | 284434 |
rs765336006 | snp | C/T | 1.64776e-05 | 0.00287028 | missense | NWD1 | GRCh38.p7 | 19:16779415 | ATGGCATCATGGCTG[C/T]GTGGGACATGGAAGA | 284434 |
rs765386877 | snp | A/T | 1.65641e-05 | 0.00287781 | intron-variant | NWD1 | GRCh38.p7 | 19:16779499 | GCTTTGTGGTCAGCT[A/T]CCATAGTGAAAAGTT | 284434 |
rs765387132 | snp | A/G | 2.00074e-05 | 0.0031628 | intron-variant | NWD1 | GRCh38.p7 | 19:16762184 | TGCAACCTCCACCCT[A/G]CCTGGCATTGCTCAC | 284434 |
rs765415711 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16785906 | GTCCCACTCTGTCGC[A/C]CAGGCTGGAGTGCAA | 284434 |
rs765461214 | snp | C/G | 0.000162853 | 0.0090222 | synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744687 | GCTGGGGCTCATCAC[C/G]CAGGAGCAGTGGCAG | 284434 |
rs765464961 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16798204 | AGTTGTCCAAGCTGG[A/C]GAGAAAAGTAGATGG | 284434 |
rs765465315 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16799309 | CAAGTGAGTCTCCTG[C/T]CTCAGCCTCCCGAGT | 284434 |
rs765466981 | snp | C/T | 1.72516e-05 | 0.00293692 | intron-variant | NWD1 | GRCh38.p7 | 19:16814987 | GATTGGACCTCTACA[C/T]CCCATTTTTCTCATT | 284434 |
rs765510846 | in-del | -/GAAAAGAAAT/GAAAT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16737994 | GAAAAGAAAAGAAAA[-/GAAAAGAAAT/GAAAT]GAAAAGAAAAGAAAA | 284434 |
rs765517104 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16741200 | AGCCTTATCCCCCTT[C/T]GCTGTCCCTCTTCTT | 284434 |
rs765517823 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16755913 | CTGTCTCCCAACGTA[C/T]CTCAAAATTGATGTA | 284434 |
rs765518823 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16812317 | AAAAACAAAAACAAA[A/T]AAAAGGCCTGGTTCC | 284434 |
rs765545501 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16726777 | AACACTGCTGACAAC[C/T]GGGAACAGATCATTC | 284434 |
rs765568205 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16762718 | CCCTGCTGGACTGGG[A/G]AGGCTGGAGGCAGGA | 284434 |
rs765592001 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16722687 | TCCTGGGAAGTGACC[G/T]CTAAGCCCTTGGAAT | 284434 |
rs765633905 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16773809 | TCCATCCTTTCATTC[-/A]ACCTTCCTACTCTTC | 284434 |
rs765658420 | snp | C/G | 1.65007e-05 | 0.00287229 | missense | NWD1 | GRCh38.p7 | 19:16765099 | CTGCTGGATGACTTT[C/G]ACCTGTGTGCCCCTC | 284434 |
rs765674939 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16763060 | ACTGAGATTACAGGC[A/G]TGTAATTACAGGTGG | 284434 |
rs765737824 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751310 | AGGTATGGATGAGGA[A/G]TCAAAAGTAACAAGC | 284434 |
rs765748988 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16801029 | ACACCTCTAATACCA[A/G]CACTTTGGGAGGCCA | 284434 |
rs765818323 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16728035 | CATAGCACTCCAGCC[C/T]GAGCAACAGAGCAAG | 284434 |
rs765827034 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16788026 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 284434 |
rs765894847 | snp | A/G | 1.83569e-05 | 0.00302954 | intron-variant | NWD1 | GRCh38.p7 | 19:16765229 | AGGAGTGACCAGGAC[A/G]GGCACTGACTTCTAG | 284434 |
rs765910940 | snp | A/G | 1.73598e-05 | 0.00294611 | synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749728 | GATGCCAAGGCTGCT[A/G]GGGCACAAGACAGTG | 284434 |
rs765940201 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16770281 | ATACTGAGTAAGCTC[G/T]CAAGAGATCTGATGG | 284434 |
rs765944711 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16814341 | TTCCTGATTTCAGTA[C/T]GCCTTTGTCACTTTC | 284434 |
rs765946181 | snp | C/T | 1.65206e-05 | 0.00287403 | missense | NWD1 | GRCh38.p7 | 19:16773153 | TGTACACAGAACTGC[C/T]GGCCAGACTCCATTT | 284434 |
rs765948496 | in-del | -/TC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754598 | TCCTTCCATCCATCA[-/TC]TGTCTTCCTTTTATC | 284434 |
rs765974319 | in-del | -/TTGT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16730107 | GTGGGCAGATCACAA[-/TTGT]GGTCAGGAGATTGAA | 284434 |
rs765977109 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16795665 | CAGGTTATCTGCCTG[A/C]GTCTGCCTCCCAAAG | 284434 |
rs765984383 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16730538 | AGAAAACATAGTGAG[A/G]CTCCTTCTCTACAAA | 284434 |
rs766016710 | snp | G/T | 1.73087e-05 | 0.00294177 | missense, intron-variant | NWD1 | GRCh38.p7 | 19:16749822 | ATCTGCTTCCAGGTG[G/T]GCCTGGCCTATGGGC | 284434 |
rs766028372 | snp | C/T | | | synonymous-codon, intron-variant | NWD1 | GRCh38.p7 | 19:16749884 | CCACACCAGGGTGGT[C/T]CAGTTTTTCCATACC | 284434 |
rs766083666 | in-del | -/CATC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754794 | ATCATCTCTATCATC[-/CATC]CATCCATCCATCCAT | 284434 |
rs766084637 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16775175 | AATGCTAAGAGACAC[G/T]AAGTACAATGCATGG | 284434 |
rs766086878 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16781541 | GAATCGCTTGAGCTC[A/G]GGAGATTGGGGCTAC | 284434 |
rs766091256 | snp | C/T | 3.38553e-05 | 0.00411418 | intron-variant | NWD1 | GRCh38.p7 | 19:16761929 | ACAAGCAGCCACCTT[C/T]GAGCTTGATGGGTCA | 284434 |
rs766141176 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16740727 | TCTGCCCACCCTATT[C/T]TCCCAAAGTGCTGGG | 284434 |
rs766180608 | snp | C/G/T | 6.61052e-05 | 0.00574881 | synonymous-codon, utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16797871 | CATCACGGGGTCCCT[C/G/T]GATGCGCTCATTCAG | 284434 |
rs766213010 | snp | A/C | 1.64757e-05 | 0.00287012 | missense | NWD1 | GRCh38.p7 | 19:16791438 | GCATGGCCGTGCTGG[A/C]CTCCCAGGCCACACT | 284434 |
rs766220747 | in-del | -/A | 0.000544478 | 0.0164907 | intron-variant | NWD1 | GRCh38.p7 | 19:16812699 | AACAAACAAACAAAC[-/A]AAAAAACCCAAGAAA | 284434 |
rs766229748 | snp | C/T | 4.94173e-05 | 0.00497053 | intron-variant, synonymous-codon | NWD1 | GRCh38.p7 | 19:16812804 | TGACAAGTATGTGTA[C/T]GTGGGCTTAAAGGAT | 284434 |
rs766282847 | snp | C/T | 5.18919e-05 | 0.00509345 | intron-variant | NWD1 | GRCh38.p7 | 19:16814980 | TGTGTAGGATTGGAC[C/T]TCTACACCCCATTTT | 284434 |
rs766320660 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16771170 | TAAAAATAGATAGAT[A/G]GCTGGGCACAGTGGC | 284434 |
rs766320802 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16758216 | TGCAACCAAGAAACC[A/G]CATTTTGAATTTTAT | 284434 |
rs766321913 | in-del | -/TGT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16741367 | TTTGTTTTGTTTTTG[-/TGT]TTTTTTTTTTTTTTT | 284434 |
rs766333892 | snp | C/T | 1.66192e-05 | 0.00288259 | intron-variant | NWD1 | GRCh38.p7 | 19:16791342 | CTTCCTCTTCATTAT[C/T]CTATTAGATCAATGC | 284434 |
rs766358315 | snp | C/T | 3.34024e-05 | 0.00408657 | missense | NWD1 | GRCh38.p7 | 19:16750159 | AGCAGATGATCCAAC[C/T]CCTGCTGGCAGCTGC | 284434 |
rs766361122 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16802156 | GGACGTGGTGGCGGG[C/T]ACCTGTAATCCCAGC | 284434 |
rs766375295 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16738126 | CTTGTTTACACATTG[A/T]TTAGCCCTGCTTTCA | 284434 |
rs766391586 | snp | C/T | | | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718978 | TACAGGTGCAAACCA[C/T]CACGCCCAGCTAATT | 284434 |
rs766403838 | snp | A/G | 1.68269e-05 | 0.00290055 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750229 | GGCCAGCCTCCCAGA[A/G]TGTGGGAACCCAGGG | 284434 |
rs766420999 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16745188 | AAGGGGAAATTCCTT[A/T]TAAAACCATCAGATC | 284434 |
rs766462201 | snp | A/G | 0.00158186 | 0.028079 | intron-variant | NWD1 | GRCh38.p7 | 19:16736796 | TTACTCCTCCAGGAT[A/G]TGCCCCCTGCTTTCT | 284434 |
rs766504997 | snp | C/G | 1.67156e-05 | 0.00289093 | intron-variant | NWD1 | GRCh38.p7 | 19:16797910 | AGATCTGGGACCCTT[C/G]ATCCTCACCTCCACC | 284434 |
rs766517809 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764208 | TACCCTACAGTGCAC[A/G]GGACACCCTACCACA | 284434 |
rs766524629 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754891 | ATTCATCCACCCATC[C/T]GTCATATCTATCTAT | 284434 |
rs766547486 | snp | C/T | 3.29962e-05 | 0.00406165 | intron-variant | NWD1 | GRCh38.p7 | 19:16759216 | AAGCCCCACTGGTCC[C/T]CCCTTCAGACACGGT | 284434 |
rs766558401 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16796822 | ATGATGAGCCAAATA[C/G]GCAGTCCCTGCCCTC | 284434 |
rs766558513 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16810882 | TTCATTTATTTATTT[C/T]TGAGGCAGGGTCTTA | 284434 |
rs766563299 | snp | C/T | 3.2987e-05 | 0.00406108 | intron-variant | NWD1 | GRCh38.p7 | 19:16779302 | CTGAATACTTGGACA[C/T]AGGAACTGAGATCAT | 284434 |
rs766571456 | snp | C/T | 0.000208576 | 0.01021 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749715 | AGCTGGCTGAGCAGA[C/T]GCCAAGGCTGCTGGG | 284434 |
rs766573843 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16740068 | TTGAGAGGCTAAAGC[C/T]GGAGGATCGTGTGAT | 284434 |
rs766575590 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16765307 | CATACCTTTCCTGTC[C/T]AAACATGTGAATTTT | 284434 |
rs766576547 | snp | A/G | 1.64863e-05 | 0.00287104 | synonymous-codon, missense | NWD1 | GRCh38.p7 | 19:16797769 | ATTCTTGGCGGACTC[A/G]AGGGGCTTTCGCCGA | 284434 |
rs766611413 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16809867 | TGGCTGCTCCGTGCT[A/G]TTTCTTTATCCAACT | 284434 |
rs766624563 | snp | C/T | 0.00172861 | 0.0293482 | synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744529 | CCAAGTGACCTGGAG[C/T]TGGTGGCACGATACT | 284434 |
rs766630044 | snp | C/T | 1.6477e-05 | 0.00287024 | missense | NWD1 | GRCh38.p7 | 19:16779385 | AGGAGAAGCTGCTGG[C/T]GATTGGCACCCAGGA | 284434 |
rs766657548 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16720704 | GGACTACAGGTGTCC[A/G]CCACATGCCCGGCTA | 284434 |
rs766659785 | snp | A/G | | | utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16724434 | GGCGATGGAGGAGCC[A/G]GCATTCCAACCAGGC | 284434 |
rs766686156 | snp | C/G/T | 3.32029e-05 | 0.00407438 | missense | NWD1 | GRCh38.p7 | 19:16762110 | TCACTCTGCCACTTG[C/G/T]GGGGAAACCACTGAA | 284434 |
rs766742177 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16733610 | GTTTGTATATTTATT[A/G]CTAAGAAAGAAGCAG | 284434 |
rs766781920 | snp | A/G | 1.64963e-05 | 0.00287192 | utr-variant-3-prime, missense | NWD1 | GRCh38.p7 | 19:16815226 | CCAGGCAGAGAGAGG[A/G]GCTAGTTGCAGCTGC | 284434 |
rs766791847 | snp | A/C | 1.71331e-05 | 0.00292682 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815350 | TAAAAATAAAAAAAC[A/C]CTGTGGGGGTATGGG | 284434 |
rs766800152 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16785267 | ATGTAATCCTAGCAG[A/T]TTGGGAGGTTGAGGC | 284434 |
rs766800606 | snp | A/G | 1.93265e-05 | 0.00310851 | intron-variant | NWD1 | GRCh38.p7 | 19:16789226 | TTGTAAAGGAAAGCT[A/G]AGACCAGAGCATTCA | 284434 |
rs766806955 | in-del | -/CACCC | 1.64776e-05 | 0.00287028 | frameshift-variant | NWD1 | GRCh38.p7 | 19:16779372 | CATGGGGTGTGGAGG[-/CACCC]AGAAGCTGCTGGTGA | 284434 |
rs766838542 | snp | C/G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790229 | TTGGGAACTCAGTGA[C/G/T]CTTGGTTGTGTCATT | 284434 |
rs766919970 | snp | C/T | 8.27274e-05 | 0.00643093 | missense | NWD1 | GRCh38.p7 | 19:16807763 | AAGCAATCAACTGCA[C/T]GTCCCTGAGCAAGTG | 284434 |
rs766937039 | snp | C/T | 1.67764e-05 | 0.00289619 | intron-variant | NWD1 | GRCh38.p7 | 19:16765005 | GGGAGGTAGGCACTT[C/T]CCACATCCTCCCCCC | 284434 |
rs766973283 | in-del | -/CAAAGGTGGGAGGATCGTTTGAGCCCTGGAGT | 1.64773e-05 | 0.00287026 | frameshift-variant | NWD1 | GRCh38.p7 | 19:16808035 | TTGCCTGTGTGGAGG[lengthTooLong]TCAGCCACAAGGAGC | 284434 |
rs766990913 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16742101 | GTAAATAGGCCAGGC[A/G]CAGTGGCTCATGCCT | 284434 |
rs767000359 | in-del | -/ACT | 1.65296e-05 | 0.00287481 | cds-indel | NWD1 | GRCh38.p7 | 19:16762075 | TCAGGGACCTGGAGC[-/ACT]CAGGGTACCAAGAAG | 284434 |
rs767023525 | snp | A/C | | | missense | NWD1 | GRCh38.p7 | 19:16765102 | CTGGATGACTTTGAC[A/C]TGTGTGCCCCTCACC | 284434 |
rs767035716 | snp | G/T | 1.68179e-05 | 0.00289977 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749281 | GGACCGGCTCGCGGA[G/T]GGCTGCCTGGACGCT | 284434 |
rs767040114 | snp | C/G | 1.65718e-05 | 0.00287848 | synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749377 | GACCCACCGCCTGCC[C/G]TGGAGCCGCGACTTG | 284434 |
rs767043072 | snp | C/T | | | downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16818335 | GGATGCCGAAAAGCT[C/T]AGCAATCATGACAAA | 284434 |
rs767056392 | snp | C/T | 0.000114009 | 0.00754927 | intron-variant | NWD1 | GRCh38.p7 | 19:16794425 | TTGTAACCCTTAACC[C/T]GTGGAAGTGCCTGAC | 284434 |
rs767072070 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16812508 | ACCCCATTTCTACTC[A/C]AAATACAAAAATTAG | 284434 |
rs767081433 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16781460 | ATCTCTACAAAAAAT[A/G]CAAAAATTAGCCAGG | 284434 |
rs767092579 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732943 | GTTAAAAGATGAGGC[C/T]GGGCACAGTGGCTAA | 284434 |
rs767109450 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16806998 | CTCCAGCCTGGACAA[C/T]GAAGCCAGACTCTGT | 284434 |
rs767121326 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790245 | CTTGGTTGTGTCATT[C/T]ACCATTCTGAGTCTT | 284434 |
rs767123864 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16722588 | GCCACTGTGCCTGGC[C/T]GACCCTCACTCTTAA | 284434 |
rs767138410 | in-del | -/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16739577 | ACTTCCTTCCTGCTT[-/C]CATCTTGAACCAGGC | 284434 |
rs767140544 | snp | A/G | 1.64874e-05 | 0.00287113 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16759240 | ACACGGTCTCTCGGA[A/G]GCGGAGCTGAAGGAT | 284434 |
rs767151932 | in-del | -/AA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732217 | GTGAGACTCCGTCTC[-/AA]AAAAAAAAAAAAAAA | 284434 |
rs767169613 | in-del | -/G | 1.64838e-05 | 0.00287083 | frameshift-variant | NWD1 | GRCh38.p7 | 19:16789135 | CTGAACCTCAGATCT[-/G]GAACCTTCATGTGGA | 284434 |
rs767207692 | snp | G/T | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748108 | CCTGTCTTAGCCTCT[G/T]GAGTAGTTGGGATTA | 284434 |
rs767222855 | snp | G/T | 1.71849e-05 | 0.00293124 | intron-variant | NWD1 | GRCh38.p7 | 19:16765197 | CCGAGGCATGGGTGA[G/T]TCCAGATGGCCTGGA | 284434 |
rs767233975 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751773 | GCCACTGTGCTCCAG[C/T]CTGGGCGACAAAGGA | 284434 |
rs767282131 | snp | C/T | | | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718671 | AGGTGCAAACCACCA[C/T]GCCCAGCTAATTTTT | 284434 |
rs767288209 | snp | C/T | 0.000132214 | 0.00812954 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16736734 | GTTGGAAAACATCCA[C/T]AGGGCCAGCTTTTGT | 284434 |
rs767317655 | snp | A/C | | | downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16818220 | GGATCACTTGAGCCC[A/C]GGAGATCAAGGCTGT | 284434 |
rs767325563 | in-del | -/TAT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16742884 | CACTATGTTGCCTAT[-/TAT]TATTATTATTATTAT | 284434 |
rs767355009 | snp | A/G | 3.29669e-05 | 0.00405984 | missense, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800024 | AAGGTCTGGGATCTC[A/G]GCGATGCTCATAGGT | 284434 |
rs767391096 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16747213 | GGCTAATTTTTGTAT[C/T]TTTAGTAGAGACGGG | 284434 |
rs767400559 | snp | C/T | 0.000141034 | 0.00839625 | synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744490 | AAGGAGTGGGAGGTA[C/T]TGAGGGACCATCTGA | 284434 |
rs767441760 | snp | C/T | 1.64923e-05 | 0.00287156 | missense | NWD1 | GRCh38.p7 | 19:16762029 | CAGGATCCGAGAGAG[C/T]CAAGAGGCATGGCGT | 284434 |
rs767455419 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16768881 | CTAATCCTGGCCCTG[C/T]AAACCATCCTTGAAC | 284434 |
rs767479697 | snp | C/T | 4.94866e-05 | 0.00497402 | missense | NWD1 | GRCh38.p7 | 19:16765057 | AGCTGGATTTCCTGC[C/T]GGGGCATCTCTGGGG | 284434 |
rs767489367 | snp | C/G | 1.64735e-05 | 0.00286993 | intron-variant, missense | NWD1 | GRCh38.p7 | 19:16812749 | GTTTTCAACAGAGTT[C/G]TTACTGCAGAGGGGT | 284434 |
rs767493015 | snp | C/G/T | 4.97709e-05 | 0.00498833 | missense | NWD1 | GRCh38.p7 | 19:16762106 | CTCATCACTCTGCCA[C/G/T]TTGTGGGGAAACCAC | 284434 |
rs767533171 | snp | A/G | 1.77659e-05 | 0.00298038 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807647 | GGAGGTTGCTGAGCA[A/G]CGCAAGCTCCTATTT | 284434 |
rs767533905 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16800763 | ATCCTATTCAGGAAC[A/G]CCCCACATTCATGAT | 284434 |
rs767536136 | snp | C/T | 0.000131935 | 0.00812096 | synonymous-codon, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800071 | ATTTCTGGACCGCAC[C/T]GGCCTCACCGCAGTG | 284434 |
rs767539396 | snp | A/G | 6.59022e-05 | 0.00573993 | utr-variant-3-prime, missense | NWD1 | GRCh38.p7 | 19:16815192 | AAGAACTTCAAGAAG[A/G]CAATGTGGATGGTCA | 284434 |
rs767579404 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16795964 | AAGAATGAGGTCATG[A/C]TGACAATTGAAAAGT | 284434 |
rs767589232 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16743123 | ATGTTGGCCAGACTG[C/G]TCTCGAACTCCTCTT | 284434 |
rs767608030 | snp | G/T | 1.68746e-05 | 0.00290466 | intron-variant | NWD1 | GRCh38.p7 | 19:16764992 | AGGATGAACTGGAGG[G/T]AGGTAGGCACTTCCC | 284434 |
rs767620276 | in-del | -/GTG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732675 | AAAAAAAAAGAAAAA[-/GTG]GTGAAAAAGTGCAGT | 284434 |
rs767645903 | in-del | -/TTTGTTTTGA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16723710 | TTTGTTTTGTTTTGT[-/TTTGTTTTGA]GATGGACTGTCCCTC | 284434 |
rs767671893 | snp | A/G | 3.42372e-05 | 0.00413732 | intron-variant | NWD1 | GRCh38.p7 | 19:16797705 | CTCTGGACATGAGAG[A/G]TGTAACCCCAGTTCC | 284434 |
rs767682389 | snp | C/T | 1.66269e-05 | 0.00288326 | stop-gained, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749552 | CGCCACCACCTTTGG[C/T]AGAGCTCGGAGGTCA | 284434 |
rs767697332 | snp | A/T | | | utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16724400 | GGGAGGGAGACCACT[A/T]GCTTAAGTCCTCCAG | 284434 |
rs767715901 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16738141 | TTTAGCCCTGCTTTC[A/G]AGCTATAATGGCAGA | 284434 |
rs767716021 | snp | G/T | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748739 | TGAGGTGGAAGGATC[G/T]CTTGAGCCTAGGAGG | 284434 |
rs767733729 | snp | C/T | 1.69301e-05 | 0.00290942 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749624 | GGGCAGCAGCTCAGG[C/T]ACGATGACAGCAAGC | 284434 |
rs767734483 | snp | G/T | 1.82244e-05 | 0.00301859 | missense | NWD1 | GRCh38.p7 | 19:16750393 | TGGCCCACGTGCTGG[G/T]CTACATTGTGTCTTC | 284434 |
rs767735644 | in-del | -/GTCC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764361 | ATCCACCCATCTTCT[-/GTCC]ATCCATCCATCCATC | 284434 |
rs767784198 | in-del | -/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787907 | AATAATAATAATAAT[-/C]ATCATCATCATCATC | 284434 |
rs767803667 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16736543 | CTGTCAAAAATTTTT[G/T]AAAGAAACTTTCTGC | 284434 |
rs767821226 | in-del | -/T | 2.24258e-05 | 0.00334849 | frameshift-variant | NWD1 | GRCh38.p7 | 19:16759368 | GGCTTCGTCGGGATC[-/T]GGGATACTACTTGGC | 284434 |
rs767857897 | snp | A/C | | | downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16818217 | GGAGGATCACTTGAG[A/C]CCAGGAGATCAAGGC | 284434 |
rs767858877 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16746397 | CATAAACAGTTGGCC[A/G]GGTGCGGTGGCTCAT | 284434 |
rs767874720 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16744259 | AATTAGCTGGGTATG[A/G]TGGCATGTGATTGTG | 284434 |
rs767884159 | in-del | -/C | 3.32403e-05 | 0.00407664 | frameshift-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749368 | GGTCCTCAAGACCCA[-/C]CGCCTGCCGTGGAGC | 284434 |
rs767911271 | snp | C/G | 1.66007e-05 | 0.00288098 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749197 | CCGGGAACAGGGAGC[C/G]ACCGTCTTCCTTAGA | 284434 |
rs767950781 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16738846 | TACATTATATATTAT[A/C]TATAATACATTATCT | 284434 |
rs767972886 | snp | C/T | 3.3365e-05 | 0.00408429 | intron-variant | NWD1 | GRCh38.p7 | 19:16763956 | TCTGGGTAAGGGCTG[C/T]CCCCCATCTCAGAGG | 284434 |
rs767985500 | snp | C/G | 6.58968e-05 | 0.00573969 | utr-variant-3-prime, synonymous-codon | NWD1 | GRCh38.p7 | 19:16815122 | CAGGCATGGTTATCT[C/G]ATCCGAGAGAATTTC | 284434 |
rs768017213 | snp | C/T | 1.79432e-05 | 0.00299521 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749121 | CACACTTCCTTCCCA[C/T]CTTCCCCACTTTGGC | 284434 |
rs768036247 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16735727 | TCCAGCTACTCAGGA[G/T]ACTGAGGCATAAGAA | 284434 |
rs768155349 | snp | C/T | 3.29544e-05 | 0.00405908 | intron-variant | NWD1 | GRCh38.p7 | 19:16812724 | AAGAAAAAGAGAGAT[C/T]ATATTGTCTGTTTTC | 284434 |
rs768216558 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16806877 | AACAAATTAGCTGGG[C/T]GTGGTGGTGCGCACC | 284434 |
rs768257960 | snp | C/T | 1.64781e-05 | 0.00287033 | missense | NWD1 | GRCh38.p7 | 19:16779355 | CAGGCATCACCGCCA[C/T]GGCATGGGGTGTGGA | 284434 |
rs768264428 | snp | C/T | 0.000487052 | 0.0155977 | stop-gained, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744586 | CCCACCTACGTCCTG[C/T]AGGCACCAGGTACTG | 284434 |
rs768279885 | snp | A/G | 3.29516e-05 | 0.00405891 | intron-variant | NWD1 | GRCh38.p7 | 19:16812858 | GCTGGATGGTGAGTC[A/G]TTTTGCTTTTAGGGC | 284434 |
rs768313807 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787365 | GTTGCCCCTTTTTTA[A/C]GTGGTTATTAATTTT | 284434 |
rs768329436 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16774918 | ATTTCATCGAGAAAC[C/T]GATTCCTCCATCTAC | 284434 |
rs768341227 | snp | A/G | 0.000115675 | 0.00760421 | missense, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800105 | CACAATGGAAGCTAC[A/G]TCTACTTCCCCAAAA | 284434 |
rs768362430 | snp | C/G | 1.66416e-05 | 0.00288453 | missense | NWD1 | GRCh38.p7 | 19:16750129 | AGGTGAAGCCCCTTT[C/G]CGGAAACCAAGGCCA | 284434 |
rs768380698 | snp | C/G | 1.77153e-05 | 0.00297612 | intron-variant | NWD1 | GRCh38.p7 | 19:16762143 | TGGACCGAAAGGTGA[C/G]GTACCTGGGACCCCC | 284434 |
rs768382357 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16774142 | TTCCATCCATCTACT[G/T]CCCCATCCATCCATC | 284434 |
rs768410149 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16797328 | GTTCCAAAACATCTC[-/T]TTTTTTTTTTTTTTT | 284434 |
rs768416508 | snp | A/G | 6.59739e-05 | 0.00574305 | missense | NWD1 | GRCh38.p7 | 19:16807798 | GACCGCCTGGCCATC[A/G]CCTATGACAACATCG | 284434 |
rs768420700 | snp | C/T | 5.41492e-05 | 0.00520304 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750385 | GCTCCTCGTGGCCCA[C/T]GTGCTGGGCTACATT | 284434 |
rs768426901 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16783963 | ACGTCTGTAATCCCA[A/C]CACTTCGGGAGGCCG | 284434 |
rs768433688 | snp | C/T | 4.98244e-05 | 0.00499096 | intron-variant | NWD1 | GRCh38.p7 | 19:16763802 | GGGTTTGTGTCCAAG[C/T]TGCAGTCTCCCTTCT | 284434 |
rs768483329 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16769910 | TGGCATGATCATAGC[A/G]CACAGCACCTTCAAA | 284434 |
rs768522236 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16753210 | CTGGAACTTCAGCTT[G/T]CCTTGAGCCACAGTT | 284434 |
rs768533949 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16795352 | CCATGTGTCACCCCA[A/C]AGGAAACACAAGGGG | 284434 |
rs768544050 | snp | A/G | 1.65277e-05 | 0.00287464 | intron-variant | NWD1 | GRCh38.p7 | 19:16759177 | CTGCATCCTCCAAAT[A/G]CAGAAGACATGAGAT | 284434 |
rs768568923 | in-del | -/AA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732219 | GAGACTCCGTCTCAA[-/AA]AAAAAAAAAAAAAAG | 284434 |
rs768579123 | snp | C/T | 1.71932e-05 | 0.00293195 | intron-variant | NWD1 | GRCh38.p7 | 19:16797691 | TGACCCTCAATCTCC[C/T]CTGGACATGAGAGGT | 284434 |
rs768584702 | in-del | -/ATT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16805836 | TCCTATTATTTCATC[-/ATT]AACAAGGAGTTTCTT | 284434 |
rs768637166 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16758715 | TTCGAGGTTGAGGAG[C/T]GGGCCATTTATGGTT | 284434 |
rs768651669 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16763574 | TCTGAGGCTCAGTTC[C/T]GATGCCTCTGCCTTC | 284434 |
rs768661329 | in-del | -/TCAA | 1.6534e-05 | 0.00287519 | frameshift-variant | NWD1 | GRCh38.p7 | 19:16765125 | CCTCACCTGGACTCC[-/TCAA]CCTGAGGTTGGCCTG | 284434 |
rs768692395 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16770729 | CACAGAACCTCCACC[C/T]GTGTTGCCATCGAGG | 284434 |
rs768716824 | snp | A/G | 1.66955e-05 | 0.0028892 | missense | NWD1 | GRCh38.p7 | 19:16750053 | CTCTCAGCTTGCTCG[A/G]GGGCACTGGGGGTTT | 284434 |
rs768734526 | in-del | -/T | 4.93888e-05 | 0.0049691 | intron-variant | NWD1 | GRCh38.p7 | 19:16750435 | TGTGTTTTGAAACTC[-/T]TTATTTATTTATTTA | 284434 |
rs768751641 | snp | G/T | 1.64743e-05 | 0.00287 | utr-variant-3-prime, missense | NWD1 | GRCh38.p7 | 19:16815183 | GACCCTCTTAAGAAC[G/T]TCAAGAAGGCAATGT | 284434 |
rs768754363 | snp | C/T | | | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718476 | CCGCGCCTGACCAAG[C/T]ATCTGAAACTTCTAT | 284434 |
rs768756296 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16725007 | CAAAAATTTTTATTT[-/A]ATTTTTTATTTTTTT | 284434 |
rs768778616 | snp | C/T | 0.000173811 | 0.00932068 | intron-variant | NWD1 | GRCh38.p7 | 19:16773333 | ACAAAGGTGAGTCTC[C/T]CCAGCATAGCAAAAA | 284434 |
rs768821481 | snp | A/G | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748635 | TGGAGACCAGCTTGG[A/G]CAACATAGTAAGACC | 284434 |
rs768828706 | in-del | -/TC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782995 | CCTCCCTCCCTCCTT[-/TC]TCTCTCTCTTTCTTT | 284434 |
rs768876499 | snp | C/T | 1.65663e-05 | 0.002878 | missense, utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16799959 | CCGTGAGCCTGCTGG[C/T]CCGCGGCGGGGCTTT | 284434 |
rs768886382 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16725121 | CAGGTTCACGCAATT[C/T]CCATGCCTCAGCCTC | 284434 |
rs768894771 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754569 | TTCCACCCATTCTCT[C/T]TAAAGTCCATCTATC | 284434 |
rs768918294 | snp | A/C | 1.71281e-05 | 0.00292639 | utr-variant-3-prime, missense | NWD1 | GRCh38.p7 | 19:16815297 | AATGAAACCAAATCA[A/C]ACAAATGCTCACAAG | 284434 |
rs768926934 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16750994 | TGGGAGGCCGAGGCG[A/G]GCGGATCACCCAAGG | 284434 |
rs768929616 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16757861 | GTTGAACAGCAGCCT[A/G]GCCAACATAGTGAAA | 284434 |
rs768978674 | snp | C/T | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816442 | TATAGTTCATCCCTC[C/T]CTATTCCTTGGCTCC | 284434 |
rs768983348 | snp | A/G | 1.65285e-05 | 0.00287471 | missense | NWD1 | GRCh38.p7 | 19:16773132 | TTGTTGCAGAGAGGA[A/G]CCTCCTGTACACAGA | 284434 |
rs769000946 | snp | C/T | 5.4745e-05 | 0.00523159 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16759408 | CGTGGATGGCTTCAC[C/T]CTCCTGGCCATTGCC | 284434 |
rs769003798 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16766384 | TCCAGCCTGGGTGAC[A/C]GAGCGAGACCCTGTC | 284434 |
rs769011361 | snp | A/G | 1.64909e-05 | 0.00287144 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749260 | AGACTGCGCCCTTAG[A/G]ATGGTGGACCGGCTC | 284434 |
rs769034213 | snp | A/C | | | utr-variant-3-prime, stop-lost | NWD1 | GRCh38.p7 | 19:16815329 | GTGCCTGATAGTGTA[A/C]AAAAATAAAAATAAA | 284434 |
rs769082423 | in-del | -/CATC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16753833 | ATCATCTCTATCATC[-/CATC]CATCCATCCATCCAT | 284434 |
rs769160367 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16746261 | GCTACTCAGGAGAGT[A/G]ACGTGGGAGGATTGC | 284434 |
rs769170420 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16773943 | ATCCATCCATCTATC[C/T]ATCCATCCATCCATC | 284434 |
rs769172258 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16809481 | TGGATCAAATCCTGC[A/G]CTGGCTTAGTGCTGC | 284434 |
rs769216804 | snp | A/G | 1.65094e-05 | 0.00287305 | missense | NWD1 | GRCh38.p7 | 19:16761989 | TGTAGACAGCTGGTC[A/G]AGGTGGTCCGTGAGC | 284434 |
rs769232322 | snp | C/T | 1.65457e-05 | 0.00287621 | missense, upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749202 | AACAGGGAGCCACCG[C/T]CTTCCTTAGAGAGAT | 284434 |
rs769239460 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16770871 | GTGTCCAGAACTCCA[C/T]CCAATGTGAAGATGC | 284434 |
rs769248028 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16800699 | ATCTTCTTGATGTGT[A/C]CCCAGAGAGAGAGAG | 284434 |
rs769263477 | in-del | -/ATTAC | | | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16719408 | TCCCAAAGTGCTGGG[-/ATTAC]AGGCATGAGCCACCG | 284434 |
rs769324349 | snp | C/T | 1.64923e-05 | 0.00287156 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16808083 | TCTGAGGATGCCCTG[C/T]TGTGTCTCTGGGACC | 284434 |
rs769324398 | snp | A/G | 5.0779e-05 | 0.00503855 | intron-variant | NWD1 | GRCh38.p7 | 19:16797934 | CTCCACCTCGGGAAC[A/G]GACACTGATTCTTTA | 284434 |
rs769350927 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16761266 | TATCTTCGTCTATGG[A/G]TGGACACTTGCATTG | 284434 |
rs769384392 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16772280 | TGTGGCCGGAAGATC[G/T]CTTGAGCCCAGGAGT | 284434 |
rs769386699 | snp | C/T | 5.19764e-05 | 0.0050976 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749669 | GTACTCTTTGGGCCC[C/T]CAGGCATTGGAAAGA | 284434 |
rs769392066 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16742705 | GACGGAGTTTCGCTC[C/T]TGTTGCCCAGGCTGG | 284434 |
rs769423399 | snp | G/T | 1.78973e-05 | 0.00299137 | missense | NWD1 | GRCh38.p7 | 19:16773315 | CAACTCTCAGCGGCT[G/T]TCACAAAGGTGAGTC | 284434 |
rs769461169 | in-del | -/AAA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16746690 | CAAAAAACAAAAAAC[-/AAA]AACAAAAAAAAACAG | 284434 |
rs769467216 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16786192 | TTTACTTTTTTTTTT[A/G]GAGACAGGGACTCAC | 284434 |
rs769471592 | snp | A/T | 0.000280741 | 0.0118445 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16736641 | TTTCCCAGGTCGTTG[A/T]TCTGAGGTGGGGTAT | 284434 |
rs769484141 | snp | A/G | 3.29864e-05 | 0.00406105 | intron-variant | NWD1 | GRCh38.p7 | 19:16812702 | CAAACAAACAAACAA[A/G]AAACCCAAGAAAAAG | 284434 |
rs769518496 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16784886 | GTGAGCCGAGATCGC[A/G]CCACTGCACTCCAGC | 284434 |
rs769545360 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751842 | AAGGAAGGAAGGAAG[A/G]TAGTAAGAAAGAAAA | 284434 |
rs769551282 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16761513 | AAGAGCACACCACCA[C/T]GCCCAGCTAATTTTT | 284434 |
rs769552848 | snp | C/G | 1.67798e-05 | 0.00289648 | missense | NWD1 | GRCh38.p7 | 19:16789180 | TTGTGTATTCAGCAT[C/G]TGGCTCAAAGGTAAC | 284434 |
rs769555044 | snp | A/G | 8.26453e-05 | 0.00642774 | missense | NWD1 | GRCh38.p7 | 19:16763916 | TGCTTCACTCGGGCC[A/G]CCTGGAGGAGCTGAA | 284434 |
rs769597727 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16750483 | TTTAGAGATGGAGGT[C/G]TGGCTATGTCACCCA | 284434 |
rs769602461 | snp | A/T | 1.66554e-05 | 0.00288573 | utr-variant-3-prime, missense | NWD1 | GRCh38.p7 | 19:16815268 | AGGACTTGGAGTCAG[A/T]AAGTGCCCAGGGAAA | 284434 |
rs769648563 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16762840 | CCCAGGCTGGAGTTC[A/G]CTGGCATGATCTCAG | 284434 |
rs769679299 | snp | C/G | 1.69576e-05 | 0.00291179 | intron-variant | NWD1 | GRCh38.p7 | 19:16763991 | AGCCTGGTGACTGCA[C/G]CACGCTCCAGTCTTC | 284434 |
rs769686117 | in-del | -/TGAC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16785584 | AAAGAAAAAAGAGGA[-/TGAC]TGACTGTTTTCTGAG | 284434 |
rs769699990 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16806742 | TAAATAGGCTGGGCG[C/T]GATGGCTCATGCCTG | 284434 |
rs769701370 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16794047 | CACAGGGGTGTACCA[A/C]CATGCCCAGCTAAAA | 284434 |
rs769717910 | in-del | -/T | 1.69795e-05 | 0.00291367 | frameshift-variant, intron-variant | NWD1 | GRCh38.p7 | 19:16749879 | ACGCCCACACCAGGG[-/T]TGGTCCAGTTTTTCC | 284434 |
rs769722720 | snp | C/T | 3.39334e-05 | 0.00411892 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750305 | ACCGTGCCTGTCCCG[C/T]TGGCCACCACCGCAG | 284434 |
rs769740730 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16721934 | TGAGCAACACAGTGA[A/G]ACTCCCGTCCCTACA | 284434 |
rs769799189 | snp | C/T | 1.64756e-05 | 0.00287011 | missense | NWD1 | GRCh38.p7 | 19:16807975 | CTCTTTCTTTACGAG[C/T]GTGCAACTTCCAAAG | 284434 |
rs769799201 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16727650 | CCAGCGGTGTGACCA[A/T]CTTCATCAGTTCCAC | 284434 |
rs769843259 | snp | A/G | 6.83691e-05 | 0.00584635 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807677 | TACGGGCCTCGTGTC[A/G]GGGGTCGTCCTTGTG | 284434 |
rs769857719 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16730042 | TTAAAACTATTTATG[A/G]GCCGGGCGCAGTGGC | 284434 |
rs769858128 | snp | A/G | 3.3162e-05 | 0.00407184 | intron-variant | NWD1 | GRCh38.p7 | 19:16761975 | CTGTATACCCTCTCT[A/G]TAGACAGCTGGTCGA | 284434 |
rs769865412 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16781987 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 284434 |
rs769872543 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16813190 | TTGGGTGTCTGAGTT[G/T]GTTGTGAGATGGAGC | 284434 |
rs769896278 | snp | A/T | 2.27095e-05 | 0.0033696 | missense, intron-variant | NWD1 | GRCh38.p7 | 19:16794521 | CTGTGAGGTTCCTGG[A/T]GGTCTCTGAAGATGA | 284434 |
rs769923569 | snp | C/T | 0.000144498 | 0.00849872 | intron-variant | NWD1 | GRCh38.p7 | 19:16745197 | TTCCTTATAAAACCA[C/T]CAGATCTTGTGAGAC | 284434 |
rs769925750 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16795193 | GCTTTTGGCCCAGCC[C/T]GCGGCTCCCATGGCC | 284434 |
rs769952019 | snp | A/T | 1.64825e-05 | 0.00287071 | missense | NWD1 | GRCh38.p7 | 19:16797849 | TTGGTACTGAGAACA[A/T]CCTGATCATCACGGG | 284434 |
rs769955665 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16740304 | AGTCTGTCTCTTAAG[-/A]AAAAAAGAAGAAAAA | 284434 |
rs770031086 | in-del | -/G | 0.000713012 | 0.0188679 | intron-variant | NWD1 | GRCh38.p7 | 19:16745174 | GAGAGCCAAGCGAAA[-/G]GGGGAAATTCCTTAT | 284434 |
rs770036168 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16791807 | CAACCTCCGCCTCTC[A/G]GGTTCAAGCGATTCT | 284434 |
rs770044694 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16763723 | TTCCATTGCATTCTC[A/G]TCCACTCCAGCACTG | 284434 |
rs770044869 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16737453 | GGAAATATGGGGTCT[C/T]ACTATGTTGCCCAGG | 284434 |
rs770051881 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16796048 | ATGTGAAGGTTGGGT[A/C]ATCTCTCTCAGTGTG | 284434 |
rs770053239 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16742952 | GAGTCTTGCTCTGTC[A/G]CCCAGGCTGGAGTGT | 284434 |
rs770074174 | snp | C/T | 6.59141e-05 | 0.00574045 | missense | NWD1 | GRCh38.p7 | 19:16791501 | TGTGGAGCTCAGCTA[C/T]GGGAAAACTTCAGGG | 284434 |
rs770084041 | snp | A/T | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748540 | GATTAATAATGGCTA[A/T]ATCAGGCCGGGCGCA | 284434 |
rs770098715 | snp | A/G/T | 3.31489e-05 | 0.00407107 | synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749428 | TCACGCCTGCTACCT[A/G/T]AAGGAGCTGGGTGAG | 284434 |
rs770103468 | snp | A/G | 3.39974e-05 | 0.00412281 | missense, intron-variant | NWD1 | GRCh38.p7 | 19:16749876 | CTGGACGCCCACACC[A/G]GGGTGGTCCAGTTTT | 284434 |
rs770128484 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16778364 | TTGGCAAATATATAT[C/T]TTTTTTCTTTAGGAC | 284434 |
rs770132611 | in-del | -/AA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16739332 | CCCTATCTCTACCAA[-/AA]AAAAAAAAAAAAAAA | 284434 |
rs770154919 | snp | C/T | 1.68202e-05 | 0.00289996 | missense | NWD1 | GRCh38.p7 | 19:16749978 | GACCTGGACTCTGTC[C/T]GCCATGCTCGGAGGG | 284434 |
rs770161494 | snp | A/G | 1.81112e-05 | 0.0030092 | splice-acceptor-variant | NWD1 | GRCh38.p7 | 19:16807585 | TTTTCTTCCCTGGCA[A/G]GCGAGGAACAAGATT | 284434 |
rs770201238 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16736282 | CTGTCCAGGCTGGCA[G/T]GCAGTAGTACAATAA | 284434 |
rs770205065 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16743005 | GCAACCTTCGCCTCC[C/T]GGCTTCAAGCAAGTC | 284434 |
rs770216491 | snp | A/G | 1.65987e-05 | 0.00288082 | missense | NWD1 | GRCh38.p7 | 19:16791609 | CCGGGTTTAGCAATG[A/G]CTCCATCTCTTTGGT | 284434 |
rs770241136 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16789342 | AGGGTGCTATAAGAG[A/G]TTTCAGACTTCATAG | 284434 |
rs770257962 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16733555 | AGTGGCTCTTTGGGT[-/A]AAAAAGAAAAGAAAA | 284434 |
rs770276832 | snp | A/G | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16747818 | ATGGAATCTCACACT[A/G]CATGGCCTTTTGTGT | 284434 |
rs770283952 | in-del | -/AGGA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16735867 | AGGAAGGAAGGAAGG[-/AGGA]AGGAAGGAAGGAAGG | 284434 |
rs770337959 | in-del | -/GACTACCGCGTGGTCTACAGCAT | 1.64745e-05 | 0.00287001 | frameshift-variant | NWD1 | GRCh38.p7 | 19:16807924 | GTGGCCATTCTGACG[-/GACTACCGCGTGGTCTACAGCAT]GACCAATGGGGACCT | 284434 |
rs770368333 | snp | C/G/T | 3.36294e-05 | 0.00410046 | intron-variant | NWD1 | GRCh38.p7 | 19:16791673 | CTCAGCTTGAAAGTG[C/G/T]TCAGATGTGCTAGAA | 284434 |
rs770385137 | snp | A/G | 3.295e-05 | 0.00405881 | missense | NWD1 | GRCh38.p7 | 19:16807894 | TACACTCAGCTGCCC[A/G]AGACCCTCTCCAGCG | 284434 |
rs770389070 | snp | C/T | 1.65364e-05 | 0.0028754 | intron-variant | NWD1 | GRCh38.p7 | 19:16773121 | TCTACATCCCTTTGT[C/T]GCAGAGAGGAGCCTC | 284434 |
rs770423720 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16753680 | GGATGCTGTTTAACA[A/C]CCTACAGTGCAAAGG | 284434 |
rs770466830 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16779692 | GCCCAGGCTGGAGTG[A/C]AGTGGTGTGTTTATA | 284434 |
rs770474026 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16805974 | CCTGGGTTCAAGCGA[G/T]TCTCCTGCCTCAGCC | 284434 |
rs770498066 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16738567 | GACGGAGACTCTGTC[-/A]AAAAAAAAAAAAAAA | 284434 |
rs770544668 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16784263 | GTAGTCCCAGGCTGC[A/G]GCTGAGGCAGAAGGA | 284434 |
rs770548765 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764819 | ACACTTGGGGTGGGA[A/G]TGCTACTGGTATCTG | 284434 |
rs770560809 | snp | C/T | 6.44919e-05 | 0.00567818 | synonymous-codon, intron-variant | NWD1 | GRCh38.p7 | 19:16794487 | AAAGGGGACAGATTG[C/T]TGGAGAAGCTTCCAG | 284434 |
rs770561579 | snp | A/G | | | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744628 | GAACCAGAGGAGGCC[A/G]CCTTAACTTCTGTCC | 284434 |
rs770575519 | snp | A/G/T | 5.28112e-05 | 0.00513841 | missense | NWD1 | GRCh38.p7 | 19:16750365 | CTGGAGCAGACACAC[A/G/T]GGCAGCTCCTCGTGG | 284434 |
rs770639641 | snp | A/G | 3.35031e-05 | 0.00409273 | missense | NWD1 | GRCh38.p7 | 19:16773266 | CTGGTGCCCCTCGGA[A/G]GATTCCTCCAGCCCC | 284434 |
rs770666983 | in-del | -/T | 1.73433e-05 | 0.00294472 | frameshift-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749810 | CTGCTGAAGAGCATC[-/T]GCTTCCAGGTGTGCC | 284434 |
rs770682172 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16810356 | GGCAGGAGAATCACT[A/G]GAACCTGGAAGGCAG | 284434 |
rs770682282 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16796445 | AAAAGTCTTATTCAG[A/C]AAGAATCAATCAGGA | 284434 |
rs770707986 | in-del | -/T | 0.000905797 | 0.0212621 | intron-variant | NWD1 | GRCh38.p7 | 19:16731307 | CTCCGGGCTCCATGC[-/T]TTTTTTTATTTTTTT | 284434 |
rs770724829 | in-del | -/AAG | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817301 | AAGACTCCATCTCAT[-/AAG]AATAATAATAATAAT | 284434 |
rs770735784 | snp | A/T | 1.6722e-05 | 0.00289149 | intron-variant | NWD1 | GRCh38.p7 | 19:16797912 | ATCTGGGACCCTTCA[A/T]CCTCACCTCCACCTC | 284434 |
rs770736270 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16772236 | GAGGCGTGGTGACGT[A/G]CATCTGCAGTCCCAG | 284434 |
rs770739595 | snp | A/G | 1.65321e-05 | 0.00287502 | intron-variant | NWD1 | GRCh38.p7 | 19:16779480 | GGTGAGACTTGGGAA[A/G]TGGGCTTTGTGGTCA | 284434 |
rs770742476 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16803343 | ACAGACTTAGACAGG[C/T]CCCAGCTCCTAATAC | 284434 |
rs770745124 | snp | A/G | 6.82349e-05 | 0.00584062 | missense, intron-variant | NWD1 | GRCh38.p7 | 19:16749867 | GCCCAGGTTCTGGAC[A/G]CCCACACCAGGGTGG | 284434 |
rs770759143 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16742795 | CTTGCCTCAGGCTCC[C/T]GAGCAGCTGGGACTA | 284434 |
rs770764090 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16760156 | TGAGATCCTGTTTCA[A/G]ACTAAACTAAACTAG | 284434 |
rs770791257 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16784767 | ACCCCTGTCTCTACT[A/G]AAAATACAAAAATTA | 284434 |
rs770792857 | snp | A/G | 6.59131e-05 | 0.0057404 | missense | NWD1 | GRCh38.p7 | 19:16788994 | CAGGAGAGGTGAGGT[A/G]TGTGAAAATATTTGC | 284434 |
rs770793296 | snp | C/T | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817365 | CAGCACTTTGGGAGG[C/T]TGAGGCGGGTGGATC | 284434 |
rs770798076 | snp | A/G | 0.000134057 | 0.008186 | intron-variant, synonymous-codon | NWD1 | GRCh38.p7 | 19:16745116 | GCTGAAGGCAAAGGA[A/G]AAGCAAAGAGGCACA | 284434 |
rs770806078 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16773536 | ATATAAATTCTTCTA[A/G]TGAGCCCGATGCTAG | 284434 |
rs770813803 | snp | A/T | 1.79809e-05 | 0.00299836 | missense | NWD1 | GRCh38.p7 | 19:16807617 | CCTGGACACCTCCAG[A/T]GAGATCAGGTGTCTG | 284434 |
rs770816440 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16804545 | GGCTGCAGTGAGCTA[C/T]GATAATGCCACTGCA | 284434 |
rs770832438 | snp | A/G | 3.30371e-05 | 0.00406417 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16763911 | TCACCTGCTTCACTC[A/G]GGCCGCCTGGAGGAG | 284434 |
rs770837045 | snp | A/T | 1.64969e-05 | 0.00287196 | missense | NWD1 | GRCh38.p7 | 19:16763838 | GCCAGGTGGCCCCGC[A/T]GCCTCTGTGGTTCTC | 284434 |
rs770902850 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764451 | ATCTCCTTATTGAGC[C/T]ATGAGCTGGTTATAA | 284434 |
rs770920307 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16741803 | TCTAGATTGATGCCT[A/G]CCTCTTTGGCTAAGA | 284434 |
rs770938104 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16811972 | AGTGAGCCGAGATCA[A/G]GCTACTGCACCTCAG | 284434 |
rs770978643 | snp | A/C/T | 9.89277e-05 | 0.00703248 | utr-variant-3-prime, missense | NWD1 | GRCh38.p7 | 19:16815052 | TGACAGTCCAGTTTG[A/C/T]CCATGCTGTGGTAAA | 284434 |
rs770995497 | snp | C/T | 3.31488e-05 | 0.00407103 | synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749416 | CAAGAACAAGACTCA[C/T]GCCTGCTACCTGAAG | 284434 |
rs771031141 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16742765 | AACCTCCGCCTCCAG[G/T]GTTCAAGCGATTCTC | 284434 |
rs771041627 | snp | C/T | 1.64735e-05 | 0.00286993 | utr-variant-3-prime, missense | NWD1 | GRCh38.p7 | 19:16815148 | ATTTCCAGTGCCTTT[C/T]AGCAAAAGCCTCACC | 284434 |
rs771043750 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732099 | GCTCATGCCTGTAGT[C/T]CCAGCTACTCAGGAG | 284434 |
rs771046932 | snp | C/T | 1.64768e-05 | 0.00287021 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807875 | TGGGCCAAGATACAC[C/T]TTTTACACTCAGCTG | 284434 |
rs771048060 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16745444 | TATTACTAAAATCTG[A/G]CAGGCTGAGCCCAGT | 284434 |
rs771061212 | snp | C/G/T | 3.47362e-05 | 0.00416739 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749789 | ATGAGCTCAGATGCC[C/G/T]GTGGCCTGCTGAAGA | 284434 |
rs771090617 | in-del | -/AA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751225 | GCAAAACTCGATCTC[-/AA]AAAAAAAAAAAAAAA | 284434 |
rs771113312 | snp | A/G | 5.00513e-05 | 0.00500231 | missense | NWD1 | GRCh38.p7 | 19:16765166 | CCCTCCAGCTCTGCC[A/G]CCCTGCTGTGGAGCT | 284434 |
rs771162778 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16768749 | TGTGAGCTGAATTCA[C/T]AAAGGAAGGGGGAGT | 284434 |
rs771183303 | snp | C/G | 1.64781e-05 | 0.00287033 | missense | NWD1 | GRCh38.p7 | 19:16797840 | CGGCTGTTTTTGGTA[C/G]TGAGAACAACCTGAT | 284434 |
rs771222903 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16757628 | CGGGTCCTCTGGGAG[C/T]GCCAAGTGAGGTGCC | 284434 |
rs771239999 | snp | A/G | 1.64974e-05 | 0.00287201 | missense | NWD1 | GRCh38.p7 | 19:16759289 | GAGGTCCTGCAGGAT[A/G]TGTACCGAGATTGGA | 284434 |
rs771253076 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16746370 | GTATCAAACAAACAA[A/C]CAAAGAAACAACATA | 284434 |
rs771263113 | snp | A/G | 3.33511e-05 | 0.00408344 | missense | NWD1 | GRCh38.p7 | 19:16750062 | TGCTCGGGGGCACTG[A/G]GGGTTTTGGACACCT | 284434 |
rs771267844 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787795 | AACCCATGAGACACA[G/T]GTTGCAGTGAGCCAA | 284434 |
rs771268940 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16746691 | CAAAAAACAAAAAAC[-/A]ACAAAAAAAAACAGT | 284434 |
rs771293066 | snp | A/G | 3.15313e-05 | 0.00397047 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16759381 | TCTGGGATACTACTT[A/G]GCCCGGCGGCCCGTG | 284434 |
rs771333989 | in-del | -/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16792896 | AAAAAAAAAAAAAAA[-/G]AAAGGAATCATGGTG | 284434 |
rs771387563 | snp | C/T | 1.66322e-05 | 0.00288371 | missense | NWD1 | GRCh38.p7 | 19:16750117 | AGGCCTACTGGGAGG[C/T]GAAGCCCCTTTCCGG | 284434 |
rs771403023 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16756661 | CATGCTACCAGCATC[C/T]AGTGGGTGGAGGCTT | 284434 |
rs771404065 | snp | C/T | | | intron-variant, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800267 | GGCTGGGCCCCATGG[C/T]TCACGCCTGTAATCC | 284434 |
rs771414077 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16736448 | AGTCTGGGTCTGTCT[A/G]TTATTTTTCTCATGA | 284434 |
rs771442973 | snp | C/T | 1.65864e-05 | 0.00287974 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749364 | CAGGGGTCCTCAAGA[C/T]CCACCGCCTGCCGTG | 284434 |
rs771459063 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16812966 | TAGCTGCATCCCTTA[C/G]CTTTTAGGAAGGTGT | 284434 |
rs771467090 | in-del | -/ACAACTATA | 1.80474e-05 | 0.0030039 | intron-variant, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800195 | TGGTCATTTTTGTGG[-/ACAACTATA]GTAAGGCTTGGAGCC | 284434 |
rs771510921 | snp | A/C | 1.66854e-05 | 0.00288833 | missense, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800128 | CCCCAAAATTGGGGA[A/C]AAAAACAAAGTCACT | 284434 |
rs771514396 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16723916 | GGCCGCGCTGGTCTC[C/T]GACTCCTAACCTCAA | 284434 |
rs771539822 | snp | A/G | 3.29511e-05 | 0.00405887 | missense | NWD1 | GRCh38.p7 | 19:16791482 | AGGGATGGTGTGGTC[A/G]GTCTGTGGAGCTCAG | 284434 |
rs771602253 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16737057 | CCCTCCACTTTATGT[C/T]TATAGAACTTTGGGA | 284434 |
rs771622639 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782493 | CAAACAGAAAAATGG[G/T]TGGGGGTGGAGAAGG | 284434 |
rs771636545 | snp | A/C | 1.64925e-05 | 0.00287158 | missense | NWD1 | GRCh38.p7 | 19:16765084 | GGGGGCATTGAAGAC[A/C]TGCTGGATGACTTTG | 284434 |
rs771660929 | in-del | -/TCC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764398 | CCATCCATCCATCCA[-/TCC]ATCTAACTATCCATT | 284434 |
rs771670646 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16795527 | GTTCAAGCGATTCTC[C/G]TGCCTCAGTCTCCCA | 284434 |
rs771673520 | snp | C/T | 1.65669e-05 | 0.00287805 | intron-variant | NWD1 | GRCh38.p7 | 19:16763812 | CCAAGCTGCAGTCTC[C/T]CTTCTCCTCTGCCAG | 284434 |
rs771695581 | snp | A/C | 1.80136e-05 | 0.00300108 | missense | NWD1 | GRCh38.p7 | 19:16807610 | AAGATTCCCTGGACA[A/C]CTCCAGTGAGATCAG | 284434 |
rs771706025 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16753363 | TTAGTAAAGCCAGAT[A/C]TCTCACAGGGGTGGC | 284434 |
rs771736009 | snp | C/T | 1.65026e-05 | 0.00287246 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807788 | CAAGTGCGAGGACCG[C/T]CTGGCCATCGCCTAT | 284434 |
rs771757180 | in-del | -/TTTTG | | | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718994 | CACGCCCAGCTAATT[-/TTTTG]TTTTGTTTTGTTTTG | 284434 |
rs771759901 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16736160 | CCTTATTTCTCATGA[C/G]CTTGGCAGTCTTTTT | 284434 |
rs771768368 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16730404 | CTTGGTTAAGCATAA[A/G]GGGTACAATGGCAAA | 284434 |
rs771814409 | snp | C/G | 3.35869e-05 | 0.00409784 | missense | NWD1 | GRCh38.p7 | 19:16750201 | TGAGCCCGGTGCACA[C/G]AGATTTGCTCTGGGC | 284434 |
rs771829279 | snp | A/G | 1.7396e-05 | 0.00294919 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749700 | CAGCCCTGATGTGCA[A/G]GCTGGCTGAGCAGAT | 284434 |
rs771854281 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16743982 | GCCACCGCGCCTGGC[C/T]GATATACATTTATTA | 284434 |
rs771873115 | snp | C/G | 8.24531e-05 | 0.00642026 | missense | NWD1 | GRCh38.p7 | 19:16759277 | TCCCTGGACGACGAG[C/G]TCCTGCAGGATGTGT | 284434 |
rs771896586 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16770877 | AGAACTCCACCCAAT[A/G]TGAAGATGCTGGTGC | 284434 |
rs771904053 | snp | A/G | 0.000293298 | 0.0121063 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744539 | TGGAGCTGGTGGCAC[A/G]ATACTTCCAGAGGGA | 284434 |
rs771907483 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16796248 | CAGAAGTTCAGATCA[C/G]TGAACTTCTGATCTG | 284434 |
rs771910813 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16803776 | AAAAAAAAAAAAAAA[-/T]TATCTGGGCGTGGTG | 284434 |
rs771922493 | snp | A/G | 1.64961e-05 | 0.00287189 | synonymous-codon, missense | NWD1 | GRCh38.p7 | 19:16797763 | GCGGATATTCTTGGC[A/G]GACTCGAGGGGCTTT | 284434 |
rs771954204 | snp | A/G | 3.46867e-05 | 0.00416439 | synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749767 | GCGGCTGCTGGGGAC[A/G]TCACAAATGAGCTCA | 284434 |
rs771963199 | snp | A/G | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816997 | TTCGCCATTAAAAAT[A/G]TTAAAAATAATGGCA | 284434 |
rs771975278 | snp | A/G | 1.64779e-05 | 0.00287031 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16779377 | GGGTGTGGAGGAGAA[A/G]CTGCTGGTGATTGGC | 284434 |
rs772007080 | snp | A/C | 0.000166959 | 0.00913518 | synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744630 | ACCAGAGGAGGCCAC[A/C]TTAACTTCTGTCCTA | 284434 |
rs772041169 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16744324 | TGAGGCTGCAGTGAG[C/T]CATGGTTGTACCACC | 284434 |
rs772070773 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16780684 | TTTTTTTCTGACAGG[A/G]TGTTGCTCTGTTGCC | 284434 |
rs772077963 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754328 | CATCCATCCATCCAT[C/T]CACCCATTGTTTCTA | 284434 |
rs772083264 | snp | C/G | 1.65578e-05 | 0.00287726 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749345 | CACATCACTGACATG[C/G]ACCCAGGGGTCCTCA | 284434 |
rs772083358 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16778825 | GTGGCATGAGCCACC[A/G]TGCCCGGCCATGGCC | 284434 |
rs772122055 | snp | C/T | 1.64923e-05 | 0.00287156 | missense | NWD1 | GRCh38.p7 | 19:16765076 | GCATCTCTGGGGGCA[C/T]TGAAGACCTGCTGGA | 284434 |
rs772122290 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16759948 | GCAGTGAGCCAAGAT[A/C]GCACCACTGTACTCC | 284434 |
rs772146277 | snp | C/G | 2.12073e-05 | 0.00325626 | utr-variant-3-prime, synonymous-codon | NWD1 | GRCh38.p7 | 19:16815320 | CTCACAAGTGTGCCT[C/G]ATAGTGTAAAAAAAT | 284434 |
rs772164358 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16720636 | TCTCAGTTACTGCAA[G/T]CTCTGCCTCCCAGGT | 284434 |
rs772181124 | in-del | -/CATC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16753830 | CTCCATCATCTCTAT[-/CATC]CATCCATCCATCCAT | 284434 |
rs772201438 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16772521 | CTGGTGGCGGGCACC[-/T]TGTAGTCCCAGCTAT | 284434 |
rs772206832 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16741026 | TTAGCCAGCTGTGGT[C/T]GTGGGTGCCTATAAT | 284434 |
rs772213788 | snp | C/T | 1.64868e-05 | 0.00287109 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807812 | CGCCTATGACAACAT[C/T]GTCCTGGTGCTGGAC | 284434 |
rs772225248 | in-del | -/TTGAGA | 1.64855e-05 | 0.00287097 | cds-indel, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800014 | TCATCTTTCAAGGTC[-/TTGAGA]TGGGATCTCAGCGAT | 284434 |
rs772302956 | snp | C/G | 1.65329e-05 | 0.0028751 | missense | NWD1 | GRCh38.p7 | 19:16791377 | AATCTGGAAACTGCA[C/G]AGCCGGTATTCCATA | 284434 |
rs772317853 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16719905 | AAGACGAAAGTTACT[A/G]GGATAGCCAGGGGCT | 284434 |
rs772319757 | snp | C/T | 1.64879e-05 | 0.00287118 | missense | NWD1 | GRCh38.p7 | 19:16807811 | TCGCCTATGACAACA[C/T]CGTCCTGGTGCTGGA | 284434 |
rs772353153 | snp | C/T | 0.000181586 | 0.00952679 | stop-gained | NWD1 | GRCh38.p7 | 19:16808101 | TGTCTCTGGGACCTG[C/T]AGGCACGCAAGTGGA | 284434 |
rs772371623 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16767896 | GTGGTATTTTACAGT[A/G]TTTGTCCTTTATTCT | 284434 |
rs772372349 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790915 | CACCTCTCCTTTTTT[C/T]CTCTGAATTGGGAGT | 284434 |
rs772384471 | in-del | -/GAAAAG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16737965 | GCAAGACTCTATCTC[-/GAAAAG]AAAAGAAAAGAAAAG | 284434 |
rs772405740 | snp | A/G | 1.67905e-05 | 0.00289741 | missense | NWD1 | GRCh38.p7 | 19:16749991 | TCCGCCATGCTCGGA[A/G]GGTTCCCTGGCTGCC | 284434 |
rs772407281 | snp | A/G | 4.94923e-05 | 0.0049743 | missense | NWD1 | GRCh38.p7 | 19:16761999 | TGGTCGAGGTGGTCC[A/G]TGAGCGCTACCTGTC | 284434 |
rs772422351 | in-del | -/G | 1.69704e-05 | 0.00291289 | frameshift-variant | NWD1 | GRCh38.p7 | 19:16773282 | ATTCCTCCAGCCCCC[-/G]GGGAGGACCCCTCCG | 284434 |
rs772476395 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16755609 | GGCCAGGCTGGTCTC[A/G]AACTCCTGGCCTCAA | 284434 |
rs772531165 | snp | C/T | 1.65304e-05 | 0.00287488 | stop-gained | NWD1 | GRCh38.p7 | 19:16762076 | TCAGGGACCTGGAGC[C/T]AGGGTACCAAGAAGC | 284434 |
rs772545909 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16811947 | CTTAAACCCAGGAGA[C/T]GGAGGTTGCAGTGAG | 284434 |
rs772573623 | snp | C/T | 5.04308e-05 | 0.00502124 | intron-variant | NWD1 | GRCh38.p7 | 19:16808170 | CATGTTCATGCTAGA[C/T]CCAGGCATTGGAAAA | 284434 |
rs772595761 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16726425 | ACTAGAATTGATTTT[A/C]AACTGTTTTCTTTCT | 284434 |
rs772598908 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16810747 | CACCCTGGATGACGA[C/T]ACAAGATTCTGTCTC | 284434 |
rs772645016 | in-del | -/TCCA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764365 | CCCATCTTCTGTCCA[-/TCCA]TCCATCCATCCATCC | 284434 |
rs772654304 | snp | C/T | 1.8002e-05 | 0.00300011 | missense | NWD1 | GRCh38.p7 | 19:16807612 | GATTCCCTGGACACC[C/T]CCAGTGAGATCAGGT | 284434 |
rs772668546 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782735 | ATGCAGTGGTGTGTG[C/T]CTGTAGTCCCAGCTA | 284434 |
rs772708758 | snp | A/C | 1.67309e-05 | 0.00289226 | missense, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800132 | AAAATTGGGGACAAA[A/C]ACAAAGTCACTATTT | 284434 |
rs772737263 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16796288 | TGATCATGGTGAAAC[C/G]CTGTCTCTACTAAAA | 284434 |
rs772755053 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16725247 | AGGCTCAAATGATTC[A/G]CCTGTCTTGGACTCC | 284434 |
rs772766542 | snp | C/T | 1.65116e-05 | 0.00287324 | missense | NWD1 | GRCh38.p7 | 19:16791557 | GAAGAAACACCTACC[C/T]GTGCCGTCTCAGTCC | 284434 |
rs772776726 | in-del | -/TACA | | | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16719410 | CCAAAGTGCTGGGAT[-/TACA]GGCATGAGCCACCGT | 284434 |
rs772777556 | in-del | -/TCCA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754467 | CATCTCTATTTTCCA[-/TCCA]TCCATCCATCCATCC | 284434 |
rs772779346 | in-del | -/CTTC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16761193 | TAGCAGGGATCAGTG[-/CTTC]CTTCCTTTTCATGGC | 284434 |
rs772805734 | snp | C/T | 3.29658e-05 | 0.00405978 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807830 | CCTGGTGCTGGACAT[C/T]ACCTCCGGGGACCCC | 284434 |
rs772819638 | snp | A/G | 1.66746e-05 | 0.00288739 | intron-variant | NWD1 | GRCh38.p7 | 19:16791642 | GCACCTTTACTGACT[A/G]TGATGTGAACATTAA | 284434 |
rs772857517 | snp | C/G | 1.6808e-05 | 0.00289892 | missense | NWD1 | GRCh38.p7 | 19:16750214 | CACAGATTTGCTCTG[C/G]GCCAGCCTCCCAGAG | 284434 |
rs772872054 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16799835 | GCGTATTTCTGAACT[-/A]TAGTTGTCCACAGAA | 284434 |
rs772874754 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16736273 | CTGGCTCTGCTGTCC[A/T]GGCTGGCATGCAGTA | 284434 |
rs772893531 | snp | A/C | 1.64773e-05 | 0.00287026 | missense | NWD1 | GRCh38.p7 | 19:16779378 | GGTGTGGAGGAGAAG[A/C]TGCTGGTGATTGGCA | 284434 |
rs772901986 | snp | A/G | 1.73285e-05 | 0.00294346 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749778 | GGACGTCACAAATGA[A/G]CTCAGATGCCCGTGG | 284434 |
rs772912154 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16800817 | CTACAGTTCGGAGGT[G/T]TGGCCCTACAAACCA | 284434 |
rs772917267 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16753548 | CGTCACCTCAGGATA[C/G]TTCTCCACGCCCCCC | 284434 |
rs772940528 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16763054 | CAAAGCACTGAGATT[A/T]CAGGCGTGTAATTAC | 284434 |
rs772946250 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732015 | TGAGGTCAGAAACTC[A/G]AGACTAGCCTAGGCA | 284434 |
rs772949434 | snp | A/G | 1.64936e-05 | 0.00287168 | missense | NWD1 | GRCh38.p7 | 19:16797765 | GGATATTCTTGGCGG[A/G]CTCGAGGGGCTTTCG | 284434 |
rs772986377 | in-del | -/TTCT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16778492 | TTCTTCTTCTTCTTC[-/TTCT]TTTTTTTTTTTTTGT | 284434 |
rs773012636 | snp | C/G | 0.000142399 | 0.00843679 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744518 | TGACTGCCAGGCCAA[C/G]TGACCTGGAGCTGGT | 284434 |
rs773015742 | snp | G/T | 1.7979e-05 | 0.00299819 | intron-variant | NWD1 | GRCh38.p7 | 19:16762152 | AGGTGAGGTACCTGG[G/T]ACCCCCATTCCCCAC | 284434 |
rs773043988 | snp | G/T | 1.66084e-05 | 0.00288165 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749513 | ACGGCCGGACAGGAG[G/T]TGGCGTGGCTCTACC | 284434 |
rs773103147 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16803169 | TTATTCGCTACCACA[A/G]GAACAGTATGGGGGA | 284434 |
rs773109765 | snp | A/C | 3.20816e-05 | 0.00400497 | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815332 | CCTGATAGTGTAAAA[A/C]AATAAAAATAAAAAA | 284434 |
rs773129278 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16770895 | AAGATGCTGGTGCCT[A/G]CAATCATTTATGCCT | 284434 |
rs773135704 | in-del | -/TTTT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16778495 | TTCTTCTTCTTCTTC[-/TTTT]TTTTTTTTTTGTTGT | 284434 |
rs773179323 | snp | A/G | | | synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744669 | AGCCCAGGAGGCCCG[A/G]AGGCTGGGGCTCATC | 284434 |
rs773198262 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16758996 | GCGACAGAGTGAAAC[G/T]CTGTCTCAAAAAAAA | 284434 |
rs773225871 | snp | A/G | | | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744560 | TCCAGAGGGACGAGA[A/G]TGCGTTTCCTCCCAC | 284434 |
rs773253280 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16784065 | TAAAAATTAGCTGGG[C/T]GTGGTGGTGCACACC | 284434 |
rs773284353 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16768566 | TAATATCTTTTTCTC[C/T]ACCCTTTTATGTTCA | 284434 |
rs773292497 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16767350 | CCAGGTGTGGTGGCT[C/G]ACGCCTATAATCCCA | 284434 |
rs773303389 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16746088 | GACCAGGTGTGGTGG[A/C]TCATGCCTGTAATCC | 284434 |
rs773312310 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16743983 | CCACCGCGCCTGGCC[A/G]ATATACATTTATTAA | 284434 |
rs773344565 | snp | C/T | 1.65663e-05 | 0.002878 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807755 | GGCCCGGAAAGCAAT[C/T]AACTGCATGTCCCTG | 284434 |
rs773357780 | snp | G/T | 8.24776e-05 | 0.00642122 | missense | NWD1 | GRCh38.p7 | 19:16759285 | CGACGAGGTCCTGCA[G/T]GATGTGTACCGAGAT | 284434 |
rs773373492 | snp | A/G | 1.68482e-05 | 0.00290238 | intron-variant | NWD1 | GRCh38.p7 | 19:16764997 | GAACTGGAGGGAGGT[A/G]GGCACTTCCCACATC | 284434 |
rs773441169 | snp | A/G | 1.6492e-05 | 0.00287154 | missense | NWD1 | GRCh38.p7 | 19:16765079 | TCTCTGGGGGCATTG[A/G]AGACCTGCTGGATGA | 284434 |
rs773454649 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16760103 | GAGGCCACACTGAGC[C/T]GTGACTGTACCACTG | 284434 |
rs773462179 | snp | A/G | 0.000564204 | 0.0167864 | intron-variant | NWD1 | GRCh38.p7 | 19:16797707 | CTGGACATGAGAGGT[A/G]TAACCCCAGTTCCTG | 284434 |
rs773506220 | in-del | -/GGA | 3.29552e-05 | 0.00405913 | cds-indel | NWD1 | GRCh38.p7 | 19:16779368 | CATGGCATGGGGTGT[-/GGA]GGAGAAGCTGCTGGT | 284434 |
rs773520131 | snp | C/T | 1.64958e-05 | 0.00287187 | missense | NWD1 | GRCh38.p7 | 19:16762004 | GAGGTGGTCCGTGAG[C/T]GCTACCTGTCAGGAT | 284434 |
rs773558577 | snp | C/G | 0.000165104 | 0.0090843 | missense | NWD1 | GRCh38.p7 | 19:16808103 | TCTCTGGGACCTGCA[C/G]GCACGCAAGTGGAAA | 284434 |
rs773570393 | snp | C/T | 1.64863e-05 | 0.00287104 | missense, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800057 | CGGGTGCCTGCACCA[C/T]TTCTGGACCGCACCG | 284434 |
rs773573154 | snp | A/G | 1.65343e-05 | 0.00287521 | missense | NWD1 | GRCh38.p7 | 19:16762079 | GGGACCTGGAGCCAG[A/G]GTACCAAGAAGCTCA | 284434 |
rs773578230 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16785249 | AGGCGCGGTGGCTCA[C/T]GCATGTAATCCTAGC | 284434 |
rs773615294 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16766617 | TTGAGACAGGATCTC[A/G]CTTCATTACCCAGGC | 284434 |
rs773628283 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16745802 | CATGCCTGTAGCCCC[A/G]GCTACTCAGGAGGCT | 284434 |
rs773631705 | in-del | -/AAAC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16762556 | GAAACTCTGTCTCAA[-/AAAC]AAACAAACAAACAAA | 284434 |
rs773633792 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16797898 | TCAGGTGAGGGGAGA[C/T]CTGGGACCCTTCATC | 284434 |
rs773641549 | snp | C/T | 0.000170834 | 0.00924055 | synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749275 | GATGGTGGACCGGCT[C/T]GCGGATGGCTGCCTG | 284434 |
rs773702289 | snp | A/G | 5.00421e-05 | 0.00500186 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750058 | AGCTTGCTCGGGGGC[A/G]CTGGGGGTTTTGGAC | 284434 |
rs773702556 | in-del | -/GATGGGTCACCCAG | 1.69132e-05 | 0.00290797 | intron-variant | NWD1 | GRCh38.p7 | 19:16761936 | GCCACCTTTGAGCTT[-/GATGGGTCACCCAG]GTCTATCAGTCTGTA | 284434 |
rs773735618 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16779796 | CACATACCACTATAC[C/G]CAGCTAATTTTTTAA | 284434 |
rs773748021 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16806909 | CTAGTCCCAGCTACC[C/T]GGGAGACTGAGGTGG | 284434 |
rs773749307 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16811948 | TTAAACCCAGGAGAC[A/G]GAGGTTGCAGTGAGC | 284434 |
rs773756671 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16798785 | GCACCCACCACCATG[C/G]CTGGTTAATTTTTGT | 284434 |
rs773760804 | snp | C/T | 9.94365e-05 | 0.00705042 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749200 | GGAACAGGGAGCCAC[C/T]GTCTTCCTTAGAGAG | 284434 |
rs773771970 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732278 | ACCGTGCTTGGTTAG[C/T]ATGGCAGGTGGTGTA | 284434 |
rs773786396 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16726434 | GATTTTAAACTGTTT[G/T]CTTTCTTTTTTTCTT | 284434 |
rs773815707 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16734316 | CACTCTGGGAGGCCG[A/G]GACAGGCAGATCACG | 284434 |
rs773821348 | snp | C/G | 1.80994e-05 | 0.00300822 | intron-variant | NWD1 | GRCh38.p7 | 19:16789206 | GTAACAAACATATGC[C/G]CTGTTTGTAAAGGAA | 284434 |
rs773827069 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751335 | ACAAGCATATATTGC[C/T]TTTTGGATATAGCAA | 284434 |
rs773850596 | snp | A/G | 1.6476e-05 | 0.00287014 | intron-variant | NWD1 | GRCh38.p7 | 19:16812730 | AAGAGAGATCATATT[A/G]TCTGTTTTCAACAGA | 284434 |
rs773928435 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751618 | CCAGTCTGGTCAACA[C/T]GGTGAAACCTCATCT | 284434 |
rs773947998 | snp | A/G | 1.65504e-05 | 0.00287662 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16762090 | CCAGGGTACCAAGAA[A/G]CTCATCACTCTGCCA | 284434 |
rs773949805 | snp | C/G | 3.29544e-05 | 0.00405908 | missense | NWD1 | GRCh38.p7 | 19:16779366 | GCCATGGCATGGGGT[C/G]TGGAGGAGAAGCTGC | 284434 |
rs773958477 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16769972 | CCTCCCAAGTAGCTG[G/T]GACCACAGGTGCACA | 284434 |
rs773967592 | snp | A/G | 1.65411e-05 | 0.00287581 | missense, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800109 | ATGGAAGCTACGTCT[A/G]CTTCCCCAAAATTGG | 284434 |
rs773973753 | snp | G/T | 1.64811e-05 | 0.00287059 | missense | NWD1 | GRCh38.p7 | 19:16791417 | ATGCCTCTGATCCTT[G/T]GATGTGCATGGCCGT | 284434 |
rs773999814 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16746291 | CGTCAGCCTAGGAGG[C/T]GGAGATTGCAGTGAA | 284434 |
rs774000646 | snp | A/G | 1.77382e-05 | 0.00297805 | intron-variant | NWD1 | GRCh38.p7 | 19:16762144 | GGACCGAAAGGTGAG[A/G]TACCTGGGACCCCCA | 284434 |
rs774050825 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16743932 | AGGTAATCCACCCGC[C/T]TTGGCCTCCCAAAGT | 284434 |
rs774068775 | snp | A/G | 1.71493e-05 | 0.0029282 | intron-variant | NWD1 | GRCh38.p7 | 19:16797700 | ATCTCCTCTGGACAT[A/G]AGAGGTGTAACCCCA | 284434 |
rs774105212 | snp | C/T | 1.67739e-05 | 0.00289597 | missense | NWD1 | GRCh38.p7 | 19:16750195 | GGACGCTGAGCCCGG[C/T]GCACACAGATTTGCT | 284434 |
rs774143669 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16774929 | AAACTGATTCCTCCA[A/T]CTACCCATCTACCTG | 284434 |
rs774157498 | snp | A/C | 1.68448e-05 | 0.00290209 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749612 | CTGGCCCGGCTTGGG[A/C]AGCAGCTCAGGCACG | 284434 |
rs774168133 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16774262 | ATACATCAGTTGTCC[A/G]TTCATCCAATCATCT | 284434 |
rs774210428 | snp | C/T | 1.73896e-05 | 0.00294865 | synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749690 | ATTGGAAAGACAGCC[C/T]TGATGTGCAAGCTGG | 284434 |
rs774230455 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790830 | TATAATACTAAAATT[G/T]ATTTCACTTGTTTCT | 284434 |
rs774306265 | snp | C/T | 1.65883e-05 | 0.00287991 | missense | NWD1 | GRCh38.p7 | 19:16763940 | AGCTGAAACAGGAGG[C/T]TCTGGGTAAGGGCTG | 284434 |
rs774310950 | snp | A/T | 3.30284e-05 | 0.00406363 | missense | NWD1 | GRCh38.p7 | 19:16797756 | GATCGGTGCGGATAT[A/T]CTTGGCGGACTCGAG | 284434 |
rs774355381 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16724249 | CCAACCGCCTTGTTG[A/G]TGTTTTGTTCAAGGT | 284434 |
rs774399530 | snp | A/C/G | 0.000156367 | 0.00884089 | intron-variant | NWD1 | GRCh38.p7 | 19:16773337 | AGGTGAGTCTCCCCA[A/C/G]CATAGCAAAAATCCC | 284434 |
rs774419413 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16776405 | AAACCCTGTCTCTAC[C/T]AAAAATACAAAAATT | 284434 |
rs774422039 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764669 | CATCCATGCACCAAT[A/C]CACCCAACATTCTTT | 284434 |
rs774424043 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16759004 | GTGAAACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 284434 |
rs774425626 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16725939 | CCATCATGCCATAGC[G/T]ACATTGTTTTTTTTT | 284434 |
rs774459640 | snp | C/G | 1.64743e-05 | 0.00287 | utr-variant-3-prime, missense | NWD1 | GRCh38.p7 | 19:16815185 | CCCTCTTAAGAACTT[C/G]AAGAAGGCAATGTGG | 284434 |
rs774467712 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16719832 | CCTAGTGCAAACAAT[C/T]GCTTTCATTATCCCA | 284434 |
rs774468750 | in-del | -/T | 1.67435e-05 | 0.00289335 | frameshift-variant | NWD1 | GRCh38.p7 | 19:16765173 | GCTCTGCCGCCCTGC[-/T]GTGGAGCTCCGAGGC | 284434 |
rs774470171 | in-del | -/G | 4.94833e-05 | 0.00497385 | frameshift-variant | NWD1 | GRCh38.p7 | 19:16759285 | CGACGAGGTCCTGCA[-/G]GATGTGTACCGAGAT | 284434 |
rs774475795 | snp | A/G | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16747774 | CTTTCTGTCTCTATT[A/G]ATTTGCCTGTTCTGG | 284434 |
rs774498722 | snp | G/T | 1.71956e-05 | 0.00293215 | splice-donor-variant | NWD1 | GRCh38.p7 | 19:16789191 | GCATCTGGCTCAAAG[G/T]TAACAAACATATGCC | 284434 |
rs774575662 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16730279 | GTGAGCTGAGATCAC[A/G]CCACTGCACTCCAGC | 284434 |
rs774582164 | snp | A/C | 1.77015e-05 | 0.00297497 | utr-variant-3-prime, synonymous-codon | NWD1 | GRCh38.p7 | 19:16815308 | ATCAAACAAATGCTC[A/C]CAAGTGTGCCTGATA | 284434 |
rs774604838 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16758744 | TTCTGTAGGTGTGCA[C/T]GCAGAGGAAAAGATT | 284434 |
rs774617232 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16789916 | AGAGACAGGGTTTCA[A/C]CATGTTGGCCAGGCT | 284434 |
rs774625523 | snp | A/C | 1.6902e-05 | 0.00290701 | intron-variant | NWD1 | GRCh38.p7 | 19:16764985 | ACCTCCCAGGATGAA[A/C]TGGAGGGAGGTAGGC | 284434 |
rs774634741 | snp | A/G | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748653 | ACATAGTAAGACCCC[A/G]TCTCTACAAAAAATA | 284434 |
rs774645348 | snp | A/G | 4.95765e-05 | 0.00497853 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16773139 | AGAGAGGAGCCTCCT[A/G]TACACAGAACTGCTG | 284434 |
rs774652029 | snp | A/G | 1.69502e-05 | 0.00291115 | missense | NWD1 | GRCh38.p7 | 19:16807684 | CTCGTGTCGGGGGTC[A/G]TCCTTGTGTTCCCCC | 284434 |
rs774660746 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16724251 | AACCGCCTTGTTGAT[A/G]TTTTGTTCAAGGTGG | 284434 |
rs774735164 | snp | C/G | 5.21599e-05 | 0.00510658 | synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749692 | TGGAAAGACAGCCCT[C/G]ATGTGCAAGCTGGCT | 284434 |
rs774750362 | in-del | -/AAAA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732217 | GTGAGACTCCGTCTC[-/AAAA]AAAAAAAAAAAAAAG | 284434 |
rs774753747 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16766406 | GACCCTGTCTCAAAA[C/T]GAACAAACCAAAAAA | 284434 |
rs774778849 | snp | C/T | 2.04748e-05 | 0.00319953 | intron-variant | NWD1 | GRCh38.p7 | 19:16759452 | AGGCAGCAGTGGCAG[C/T]GACACTGTCTGGGTG | 284434 |
rs774783590 | in-del | -/GTCC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764364 | ACCCATCTTCTGTCC[-/GTCC]ATCCATCCATCCATC | 284434 |
rs774795279 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16810533 | AGCACTTTGGGAGGC[C/T]GAGGCAGGGGGATTG | 284434 |
rs774803857 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16760347 | CACTGCAGCCTCAAA[C/T]TCCTGGACTCAAGCA | 284434 |
rs774804919 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16765018 | TTCCCACATCCTCCC[C/G]CCTTCTCTCCCTCAG | 284434 |
rs774866258 | in-del | -/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16771660 | AAGTTCCCTGCAAAG[-/C]CCCTTGATTGACAAC | 284434 |
rs774873619 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16796604 | TTGCCTGCCTCCTGC[C/T]GCTATCCCTTCCTTT | 284434 |
rs774921895 | snp | G/T | 1.69241e-05 | 0.00290891 | synonymous-codon, intron-variant | NWD1 | GRCh38.p7 | 19:16749917 | CCTCCACACTGTCTC[G/T]TGCAGAAACTTCGAG | 284434 |
rs774939020 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16739869 | TTCCCTTGCTCTGAT[C/T]CCACAGATTGGAGCA | 284434 |
rs774952944 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16745677 | CCCAGGAGGCAGAGG[A/C]TGTGGTAAGCCAAGA | 284434 |
rs774972132 | snp | A/G | 1.69683e-05 | 0.00291271 | intron-variant | NWD1 | GRCh38.p7 | 19:16797938 | ACCTCGGGAACAGAC[A/G]CTGATTCTTTAGGGA | 284434 |
rs775001902 | snp | A/G | 1.65425e-05 | 0.00287593 | missense | NWD1 | GRCh38.p7 | 19:16762085 | TGGAGCCAGGGTACC[A/G]AGAAGCTCATCACTC | 284434 |
rs775026034 | snp | C/G | 1.69666e-05 | 0.00291256 | missense | NWD1 | GRCh38.p7 | 19:16773281 | GGATTCCTCCAGCCC[C/G]CGGGAGGACCCCTCC | 284434 |
rs775075815 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16781314 | TGCAGCTTGATATAC[A/G]TAGGACCACATTGGC | 284434 |
rs775081121 | snp | C/G | 1.64923e-05 | 0.00287156 | stop-gained | NWD1 | GRCh38.p7 | 19:16762014 | GTGAGCGCTACCTGT[C/G]AGGATCCGAGAGAGC | 284434 |
rs775144052 | snp | A/G | 1.64841e-05 | 0.00287085 | intron-variant | NWD1 | GRCh38.p7 | 19:16812712 | AACAAAAAACCCAAG[A/G]AAAAGAGAGATCATA | 284434 |
rs775155663 | snp | C/T | 1.7959e-05 | 0.00299652 | missense | NWD1 | GRCh38.p7 | 19:16773317 | ACTCTCAGCGGCTGT[C/T]ACAAAGGTGAGTCTC | 284434 |
rs775162552 | snp | A/G | 5.00213e-05 | 0.00500081 | missense | NWD1 | GRCh38.p7 | 19:16750063 | GCTCGGGGGCACTGG[A/G]GGTTTTGGACACCTT | 284434 |
rs775173932 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16807169 | CTCCAGAATACTGTC[A/T]CAAAAAAAAAAAAAA | 284434 |
rs775210750 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751943 | GAAAGAAGAAAGGAA[A/G]GAAAGAAAAGAAGAA | 284434 |
rs775215662 | snp | A/G | 1.6534e-05 | 0.00287519 | missense | NWD1 | GRCh38.p7 | 19:16763921 | CACTCGGGCCGCCTG[A/G]AGGAGCTGAAACAGG | 284434 |
rs775242708 | snp | C/T | | | synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744711 | GTGGCAGCACTACCA[C/T]CGGTCAGGTGAGGCC | 284434 |
rs775256892 | snp | A/G | 1.75499e-05 | 0.0029622 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16762138 | GAACTTGGACCGAAA[A/G]GTGAGGTACCTGGGA | 284434 |
rs775286731 | snp | C/T | 1.66194e-05 | 0.00288261 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749537 | CTCTACCAAGAGATC[C/T]GCCACCACCTTTGGC | 284434 |
rs775287717 | in-del | -/CCTC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782979 | CTTCTTTCCTTCCTC[-/CCTC]CCTCCCTCCCTCCTT | 284434 |
rs775289766 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16778168 | CCCATTTTACACATG[C/T]GGAAGAGGCACACAG | 284434 |
rs775306241 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16741983 | GGGTGTGGTGGTGGG[C/T]GCCTGTAGTCCCAGC | 284434 |
rs775336975 | in-del | -/TC | 5.06855e-05 | 0.0050339 | frameshift-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749933 | TGCAGAAACTTCGAG[-/TC]TCTCGTGCTCCTGCT | 284434 |
rs775368397 | snp | A/C | 1.64838e-05 | 0.00287083 | missense | NWD1 | GRCh38.p7 | 19:16797850 | TGGTACTGAGAACAA[A/C]CTGATCATCACGGGG | 284434 |
rs775368938 | snp | C/T | 1.79155e-05 | 0.0029929 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807629 | CAGTGAGATCAGGTG[C/T]CTGGAGGTTGCTGAG | 284434 |
rs775395262 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16801715 | AACAAGACCCTGTTT[C/G]AAAACAAAACAACAA | 284434 |
rs775402357 | snp | A/G | 1.78854e-05 | 0.00299038 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750379 | CGGGCAGCTCCTCGT[A/G]GCCCACGTGCTGGGC | 284434 |
rs775407522 | snp | C/T | | | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718398 | AGCTGGTCTCAAATT[C/T]CTGACCTCAGGTGAT | 284434 |
rs775433466 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16803776 | AAAAAAAAAAAAAAA[A/T]TATCTGGGCGTGGTG | 284434 |
rs775447122 | in-del | -/AT | 3.44258e-05 | 0.0041487 | intron-variant | NWD1 | GRCh38.p7 | 19:16797684 | AAGGAATGACCCTCA[-/AT]ATCTCCTCTGGACAT | 284434 |
rs775449114 | snp | A/C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16806754 | GCGCGATGGCTCATG[A/C/T]CTGTAATCCCAGCAT | 284434 |
rs775472332 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16750761 | CCATCTCAGCCTGCC[A/G]AGTAGGGTAGCTGGG | 284434 |
rs775480611 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16780133 | GCGTCCTTCAGGTCT[C/G]TCATCCCCAGCAAAG | 284434 |
rs775499597 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16721948 | AGACTCCCGTCCCTA[C/T]AAAAAATAAAAAACT | 284434 |
rs775512364 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16788476 | TGGGAGGCTGAGGCA[C/T]GAGAATCACTTGAAC | 284434 |
rs775533529 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16792475 | TGAGGTTGGGAGTTC[A/G]AGACCAGCCTGGCCA | 284434 |
rs775547674 | snp | A/G | 1.67033e-05 | 0.00288987 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749591 | TTCTGCGGACGCCAG[A/G]AACTCCTGGCCCGGC | 284434 |
rs775601515 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16726811 | GTGGGGGCTTCCTGG[A/G]CATTGTTAGATGTTG | 284434 |
rs775655708 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16726533 | CAACCTCCACCTCCT[G/T]AGTTCAAGCGATTCT | 284434 |
rs775696297 | in-del | -/AT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790655 | ATAAATAAATAAATA[-/AT]AATAAATAAATAAAT | 284434 |
rs775700946 | snp | A/G | 6.75003e-05 | 0.0058091 | intron-variant | NWD1 | GRCh38.p7 | 19:16797928 | CCTCACCTCCACCTC[A/G]GGAACAGACACTGAT | 284434 |
rs775715115 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16743002 | ACTGCAACCTTCGCC[C/T]CCCGGCTTCAAGCAA | 284434 |
rs775722346 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16786836 | GGATTACAGGCATGA[G/T]CCACCCTGCCCAGCC | 284434 |
rs775738569 | in-del | -/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16752218 | TCAGTTTTAGGGTTG[-/G]TTTTTTTTTTTTCTC | 284434 |
rs775769590 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16757765 | TACCATATCATAGAA[G/T]TTTGCAGGCCAGGTG | 284434 |
rs775775545 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16786315 | GCCCAGTCATATCCT[C/T]GTTCTGTTATTGTAT | 284434 |
rs775788154 | snp | C/T | 3.64611e-05 | 0.00426957 | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749088 | CCCATTTAGGTCAGC[C/T]GCTGACCCAATAATG | 284434 |
rs775801576 | in-del | -/G | 6.58924e-05 | 0.0057395 | frameshift-variant | NWD1 | GRCh38.p7 | 19:16807954 | TACAGCATGACCAAT[-/G]GGGACCTCTTTCTTT | 284434 |
rs775803941 | in-del | -/AAG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16776951 | TATCTGAAAAAAAAA[-/AAG]AAGAAGAAAAGGAAG | 284434 |
rs775811280 | snp | A/G | 1.64757e-05 | 0.00287012 | utr-variant-3-prime, missense | NWD1 | GRCh38.p7 | 19:16815096 | ACCACCAGTGGCTTC[A/G]TTGCCCCCACCAGGC | 284434 |
rs775842851 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16768975 | ACAGCATCCTCGGAG[G/T]TCTGCCTACTTTGGA | 284434 |
rs775846081 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16813279 | ATTCCAGCATAGAAC[C/G]CTGAGGAGCCCAAGA | 284434 |
rs775856811 | snp | A/G | 1.65312e-05 | 0.00287495 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16773127 | TCCCTTTGTTGCAGA[A/G]AGGAGCCTCCTGTAC | 284434 |
rs775863320 | snp | A/G | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16747830 | ACTACATGGCCTTTT[A/G]TGTCTGGCTTCTCTC | 284434 |
rs775908322 | snp | A/G | 4.3336e-05 | 0.00465469 | missense | NWD1 | GRCh38.p7 | 19:16759398 | CCCGGCGGCCCGTGG[A/G]TGGCTTCACCCTCCT | 284434 |
rs775916798 | snp | A/C | 1.68635e-05 | 0.0029037 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749176 | GAGCCTGCTGAGCTC[A/C]GAGGACCGGGAACAG | 284434 |
rs775940545 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16771307 | ATACAAAAATTAGCC[A/G]GGTGTGGTGGTGCAT | 284434 |
rs775991595 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16737693 | ATTCTAGAGCAGGGG[G/T]CCGGGCGTGGTGGCT | 284434 |
rs776004692 | in-del | -/T | 0.000599624 | 0.0173047 | intron-variant | NWD1 | GRCh38.p7 | 19:16807569 | TGTAAGTCATTCTCA[-/T]TTTTCTTCCCTGGCA | 284434 |
rs776060633 | snp | C/T | 3.30961e-05 | 0.0040678 | missense | NWD1 | GRCh38.p7 | 19:16759308 | ACCGAGATTGGACCC[C/T]GCCCAGCAAGGAGCT | 284434 |
rs776063380 | snp | C/G | 2.17697e-05 | 0.00329914 | missense, intron-variant | NWD1 | GRCh38.p7 | 19:16794506 | AGAAGCTTCCAGATG[C/G]TGTGAGGTTCCTGGT | 284434 |
rs776120610 | snp | C/T | 1.68581e-05 | 0.00290324 | missense | NWD1 | GRCh38.p7 | 19:16773272 | CCCCTCGGAGGATTC[C/T]TCCAGCCCCCGGGAG | 284434 |
rs776122889 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754509 | ATCCATCCATCCATC[A/G]TCTCTATCTTCCATT | 284434 |
rs776144612 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16784853 | AGAATCACTTGAACC[C/T]GGGGGGCGGAGGTTG | 284434 |
rs776166331 | snp | C/T | 3.29478e-05 | 0.00405867 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807908 | CGAGACCCTCTCCAG[C/T]GTGGCCATTCTGACG | 284434 |
rs776169591 | snp | C/G | 3.29533e-05 | 0.00405901 | missense | NWD1 | GRCh38.p7 | 19:16808006 | CGTTTCCCTTGGAGA[C/G]CCACAGGAGCCGAGT | 284434 |
rs776177980 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764838 | TACTGGTATCTGGTG[A/G]GTGGAGGCCAGGGTT | 284434 |
rs776180574 | snp | A/C | 3.47102e-05 | 0.0041658 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749795 | TCAGATGCCCGTGGC[A/C]TGCTGAAGAGCATCT | 284434 |
rs776233272 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16737564 | ACCTGGTCTAGTTTT[A/C]AGTTTTTTTTTTTTT | 284434 |
rs776247698 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16792387 | TCTTTACTAAAAGTA[C/T]AAAAATTGACCAGGC | 284434 |
rs776265398 | snp | G/T | 1.65209e-05 | 0.00287405 | missense | NWD1 | GRCh38.p7 | 19:16773155 | TACACAGAACTGCTG[G/T]CCAGACTCCATTTCT | 284434 |
rs776307020 | snp | A/G | 1.64882e-05 | 0.00287121 | stop-gained | NWD1 | GRCh38.p7 | 19:16763848 | CCCGCAGCCTCTGTG[A/G]TTCTCACATACGGTT | 284434 |
rs776323627 | snp | A/T | 0.00141143 | 0.0265278 | intron-variant | NWD1 | GRCh38.p7 | 19:16745159 | GCAGGTAAGACAGAG[A/T]GAGAGCCAAGCGAAA | 284434 |
rs776326808 | in-del | -/CTCC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764388 | TCCATCCATCCATCC[-/CTCC]ATCCATCCATCCATC | 284434 |
rs776351279 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16720774 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCA | 284434 |
rs776374720 | snp | A/T | 0.000148875 | 0.00862643 | intron-variant | NWD1 | GRCh38.p7 | 19:16779486 | ACTTGGGAAGTGGGC[A/T]TTGTGGTCAGCTTCC | 284434 |
rs776377029 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16753723 | TAGAGAATGATCCAG[A/C]CCCAGATGTTGATAG | 284434 |
rs776396869 | in-del | -/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16791902 | TGTTTTTAGTAGAGA[-/C]AGGGTTTCTCCATGT | 284434 |
rs776413881 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16756488 | CTTCAAGGGTCAACT[A/G]TATGTCTATCTGCCT | 284434 |
rs776460075 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16796547 | TGTTTTTGGTTCAAA[A/G]GTACAGTTTCACTGG | 284434 |
rs776461654 | in-del | -/T | 0.0228336 | 0.104381 | intron-variant | NWD1 | GRCh38.p7 | 19:16731315 | TCCATGCTTTTTTTA[-/T]TTTTTTTTTGACACG | 284434 |
rs776481826 | snp | A/G | 0.000140776 | 0.00838856 | intron-variant | NWD1 | GRCh38.p7 | 19:16736611 | TGCCACCTCTCTGAC[A/G]AACTTGTGTTTCTAT | 284434 |
rs776519967 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16760176 | AACTAAACTAGACTA[A/G]ACTAAACTAAACTAA | 284434 |
rs776524274 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16813002 | GGCAAAGGCAAAGGG[A/C]CCACAATCCCTCTTC | 284434 |
rs776628961 | snp | C/T | 1.65231e-05 | 0.00287424 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16763914 | CCTGCTTCACTCGGG[C/T]CGCCTGGAGGAGCTG | 284434 |
rs776642145 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16799132 | GAAGGCCCTTGAACT[C/T]ACAGCCTGAAAATTC | 284434 |
rs776669708 | in-del | -/TCTC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16773855 | CCATCCATTCATTCA[-/TCTC]TCTATCTACCTCCCA | 284434 |
rs776680690 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16807447 | ACGGTGACCTGAGAT[C/T]GTGCTATTGCACTAC | 284434 |
rs776697074 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16803401 | ATAGGAATTTGGTGG[G/T]GGGGTGGGGACACAA | 284434 |
rs776715461 | snp | A/C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16755850 | GCCTATAATCTATCT[A/C/T]TGTATATACAGTTGG | 284434 |
rs776716542 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16789422 | TTTCATCTTTTTTGA[A/G]TATCAGCATTTTAGG | 284434 |
rs776733167 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732411 | TGTTTTTGTCTTGCC[G/T]TCAGAGCTTCCTGGC | 284434 |
rs776733321 | snp | A/G | 7.18597e-05 | 0.00599372 | missense | NWD1 | GRCh38.p7 | 19:16807621 | GACACCTCCAGTGAG[A/G]TCAGGTGTCTGGAGG | 284434 |
rs776767700 | snp | A/T | 1.7013e-05 | 0.00291654 | missense, intron-variant | NWD1 | GRCh38.p7 | 19:16749873 | GTTCTGGACGCCCAC[A/T]CCAGGGTGGTCCAGT | 284434 |
rs776774941 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16812058 | GCTCATGCCTGTAAT[C/T]TCAGCACTTCGGGAA | 284434 |
rs776805006 | snp | A/G | 1.64912e-05 | 0.00287147 | missense | NWD1 | GRCh38.p7 | 19:16759229 | CCTCCCTTCAGACAC[A/G]GTCTCTCGGAGGCGG | 284434 |
rs776805099 | snp | C/T | 8.34899e-05 | 0.00646049 | missense | NWD1 | GRCh38.p7 | 19:16765169 | TCCAGCTCTGCCGCC[C/T]TGCTGTGGAGCTCCG | 284434 |
rs776806009 | in-del | -/AAA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16739331 | ACCCTATCTCTACCA[-/AAA]AAAAAAAAAAAAAAA | 284434 |
rs776814173 | snp | A/G | 1.64765e-05 | 0.00287019 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16779398 | GGTGATTGGCACCCA[A/G]GATGGCATCATGGCT | 284434 |
rs776838719 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16726655 | ATGTTGGCCAGGCTG[A/G]TTTGAACTCCTAACC | 284434 |
rs776838776 | snp | C/T | 1.64754e-05 | 0.00287009 | missense | NWD1 | GRCh38.p7 | 19:16807892 | TTTACACTCAGCTGC[C/T]CGAGACCCTCTCCAG | 284434 |
rs776843065 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16750475 | TTTTTATTTTTAGAG[A/T]TGGAGGTCTGGCTAT | 284434 |
rs776855185 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16741818 | GCCTCTTTGGCTAAG[A/T]CTCCAAGGTTGGCTG | 284434 |
rs776856455 | snp | A/C | 1.65083e-05 | 0.00287296 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16759295 | CTGCAGGATGTGTAC[A/C]GAGATTGGACCCCGC | 284434 |
rs776892089 | in-del | -/G | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817119 | CAGCCTGGACAACAT[-/G]GTGAAACCCTTCTCT | 284434 |
rs776945967 | in-del | -/AAAA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16739330 | GACCCTATCTCTACC[-/AAAA]AAAAAAAAAAAAAAA | 284434 |
rs776965279 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16786969 | TTTGTCTGTTATATG[C/T]TGCAAATATTTCCTC | 284434 |
rs776976497 | snp | A/C | 1.64762e-05 | 0.00287016 | missense | NWD1 | GRCh38.p7 | 19:16791485 | GATGGTGTGGTCAGT[A/C]TGTGGAGCTCAGCTA | 284434 |
rs776987990 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16774957 | CTGCCCATCCATTCA[C/T]CCACTCACTCATCCA | 284434 |
rs776990098 | snp | A/G | 1.64909e-05 | 0.00287144 | synonymous-codon, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800062 | GCCTGCACCATTTCT[A/G]GACCGCACCGGCCTC | 284434 |
rs776993301 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16767001 | AAGTGAAACTCTGTT[C/T]TCATTAAACATTCAC | 284434 |
rs777000586 | snp | C/T | 5.03242e-05 | 0.00501593 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749277 | TGGTGGACCGGCTCG[C/T]GGATGGCTGCCTGGA | 284434 |
rs777012404 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16728771 | AACACAGTGAAACCC[C/T]GTCTCTACTAAAAAT | 284434 |
rs777037793 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16756698 | AGACTGCTACACATC[C/T]TACAATAGGGGTCCC | 284434 |
rs777054338 | in-del | -/C | | | downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16818335 | GGATGCCGAAAAGCT[-/C]AGCAATCATGACAAA | 284434 |
rs777057909 | snp | C/T | 3.31532e-05 | 0.0040713 | synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749368 | GGTCCTCAAGACCCA[C/T]CGCCTGCCGTGGAGC | 284434 |
rs777101402 | snp | C/G | 1.64814e-05 | 0.00287061 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16788989 | TGCTGCAGGAGAGGT[C/G]AGGTGTGTGAAAATA | 284434 |
rs777111159 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787821 | GCCAAGATTATGCCA[C/G]TGAACTCCAGCCTGG | 284434 |
rs777116424 | snp | A/G | 0.000165068 | 0.00908333 | missense | NWD1 | GRCh38.p7 | 19:16791390 | CAGAGCCGGTATTCC[A/G]TATCCTGGGAGATGC | 284434 |
rs777132410 | in-del | -/TAG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16758680 | CCACTTCCCTCCCTA[-/TAG]TGTCTGTCTCAGACC | 284434 |
rs777154627 | snp | C/G | 0.00029676 | 0.0121775 | missense | NWD1 | GRCh38.p7 | 19:16763891 | AAGCTGAAGGAGTTG[C/G]CCTATCACCTGCTTC | 284434 |
rs777161938 | snp | A/G | | | intron-variant, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800272 | GGCCCCATGGCTCAC[A/G]CCTGTAATCCCAGGA | 284434 |
rs777164184 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16786308 | CCACCTGGCCCAGTC[A/G]TATCCTTGTTCTGTT | 284434 |
rs777203271 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16779258 | TTGTCTTATCTGTGA[A/T]GTGGGGGGCTCATTA | 284434 |
rs777219683 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16744097 | AATTGGAGAAAGAAT[A/T]GTAAATTGTGGCTGG | 284434 |
rs777247010 | snp | A/G | 1.6495e-05 | 0.0028718 | missense | NWD1 | GRCh38.p7 | 19:16765091 | TTGAAGACCTGCTGG[A/G]TGACTTTGACCTGTG | 284434 |
rs777296561 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16805795 | GAATGAAGTTGAGAA[A/T]CAGCTTGAAAATCAG | 284434 |
rs777303397 | snp | G/T | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748392 | TTTCAGGTATTTTCA[G/T]CAGATACCTGGGAGT | 284434 |
rs777309846 | in-del | -/G | 1.73655e-05 | 0.0029466 | frameshift-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749728 | GATGCCAAGGCTGCT[-/G]GGGCACAAGACAGTG | 284434 |
rs777314228 | in-del | -/AA | 1.64781e-05 | 0.00287033 | frameshift-variant | NWD1 | GRCh38.p7 | 19:16779375 | TGGGGTGTGGAGGAG[-/AA]GCTGCTGGTGATTGG | 284434 |
rs777320309 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16771052 | CGCTTCTAATCCCAG[C/T]ACTTTGGGAGGCCCA | 284434 |
rs777323479 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16723937 | CTAACCTCAAGTGAT[C/T]GGCCCGCCTTGGCCT | 284434 |
rs777341948 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16737296 | TTTGAGACAGAGTCT[C/T]AAAAAAGCCCAGGCT | 284434 |
rs777401293 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764727 | CATCCATTCACCAAT[A/C]CCCGTGATTCTTAAC | 284434 |
rs777430112 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790438 | GAGTCACCAACCAGA[G/T]GTACCTATTAAACAC | 284434 |
rs777432255 | in-del | -/GG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16738494 | TAATCATTTGAAACT[-/GG]GAGGCAGAGGTTGGA | 284434 |
rs777438959 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16809008 | AGGATTGATTGAGCC[C/T]GGATGCCACTGCTCT | 284434 |
rs777450574 | snp | A/G | 1.74075e-05 | 0.00295016 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807665 | CAAGCTCCTATTTAC[A/G]GGCCTCGTGTCGGGG | 284434 |
rs777465018 | in-del | -/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16741386 | TTTTTTTTTTTTTTT[-/G]AGACAGTCTTACTCT | 284434 |
rs777484146 | snp | C/T | 1.64743e-05 | 0.00287 | utr-variant-3-prime, stop-gained | NWD1 | GRCh38.p7 | 19:16815138 | ATCCGAGAGAATTTC[C/T]AGTGCCTTTCAGCAA | 284434 |
rs777504707 | snp | C/T | 1.64768e-05 | 0.00287021 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807872 | CGATGGGCCAAGATA[C/T]ACCTTTTACACTCAG | 284434 |
rs777513869 | snp | C/T | 1.67843e-05 | 0.00289687 | intron-variant | NWD1 | GRCh38.p7 | 19:16761956 | GTCACCCAGGTCTAT[C/T]AGTCTGTATACCCTC | 284434 |
rs777545288 | snp | A/G | 3.30825e-05 | 0.00406696 | utr-variant-3-prime, synonymous-codon | NWD1 | GRCh38.p7 | 19:16815254 | TGCAGGAGCTCCCCA[A/G]GACTTGGAGTCAGAA | 284434 |
rs777573130 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16765646 | CCTGGCCTAGAATTT[G/T]AAATTGAGCCTGGGA | 284434 |
rs777617904 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16797563 | ATGTTGGCCAGGCTG[A/T]TCTCGAACTCCTGAC | 284434 |
rs777657124 | snp | A/C | 6.35613e-05 | 0.00563708 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16759361 | TGGGTGCGGCTTCGT[A/C]GGGATCTGGGATACT | 284434 |
rs777658318 | snp | G/T | 3.32618e-05 | 0.00407797 | intron-variant | NWD1 | GRCh38.p7 | 19:16797891 | CGCTCATTCAGGTGA[G/T]GGGAGATCTGGGACC | 284434 |
rs777660512 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16750429 | AAGTCTCTGTGTTTT[C/G]AAACTCTTATTTATT | 284434 |
rs777668760 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16809151 | CTGGAATGCAGTGGC[A/G]CCATCTCAGCTCACT | 284434 |
rs777679036 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16771136 | AGACCCTATCTCTGT[-/A]AAAAAAAAATTAATT | 284434 |
rs777712812 | in-del | -/AGAG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16788551 | TCCAGCCTGGGTGAC[-/AGAG]AGAGTCCGTCAAAAA | 284434 |
rs777728404 | snp | A/G | | | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16721519 | ATTCAAGATCAGAAG[A/G]TTGGGGAGGAGGTGC | 284434 |
rs777732181 | snp | A/G | 7.19011e-05 | 0.00599544 | intron-variant, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800194 | TATGGTCATTTTTGT[A/G]GGTAAGGCTTGGAGC | 284434 |
rs777744298 | snp | A/G | 0.00418254 | 0.0455387 | intron-variant, missense | NWD1 | GRCh38.p7 | 19:16745075 | GACTCACAATTCCAC[A/G]TGGCTGGGGAGGCCT | 284434 |
rs777844522 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16806639 | TCACTAGAGCCTGAG[A/C]GGTTGAGGCTGCAGT | 284434 |
rs777858132 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754331 | CCATCCATCCATCCA[A/C]CCATTGTTTCTATCT | 284434 |
rs777871733 | snp | C/T | 1.65012e-05 | 0.00287234 | missense, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800090 | CTCACCGCAGTGTCC[C/T]ACAATGGAAGCTACG | 284434 |
rs777897918 | snp | C/T | 0.000260885 | 0.0114182 | stop-gained | NWD1 | GRCh38.p7 | 19:16762133 | CCACTGAACTTGGAC[C/T]GAAAGGTGAGGTACC | 284434 |
rs777931641 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16793679 | CCTCCCAGCTTCAAG[C/T]GATTCTCCTGCCTCC | 284434 |
rs777955571 | snp | A/G | 1.66468e-05 | 0.00288498 | missense, synonymous-codon | NWD1 | GRCh38.p7 | 19:16797737 | GCCGTTTCAGGCTTT[A/G]GAAGATCGGTGCGGA | 284434 |
rs777971744 | snp | A/G | 1.73375e-05 | 0.00294422 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749738 | CTGCTGGGGCACAAG[A/G]CAGTGACCGTCCTGC | 284434 |
rs778004347 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16773417 | GTCCTCTGGGACTCC[C/T]CTGTGCTAGTTGGGA | 284434 |
rs778014209 | snp | C/T | 1.64757e-05 | 0.00287012 | missense | NWD1 | GRCh38.p7 | 19:16791477 | TGTCCAGGGATGGTG[C/T]GGTCAGTCTGTGGAG | 284434 |
rs778019841 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16720637 | CTCAGTTACTGCAAG[C/T]TCTGCCTCCCAGGTT | 284434 |
rs778060523 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16769286 | GGCCAACAGGGTGAA[A/C]CCCCATCTCTACTAA | 284434 |
rs778066287 | snp | A/G | 1.69795e-05 | 0.00291367 | intron-variant | NWD1 | GRCh38.p7 | 19:16808184 | ACCCAGGCATTGGAA[A/G]ACTGATAGATAGCCA | 284434 |
rs778070241 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16814581 | TGTAATCTGATACAT[A/G]GTAAACTATAACACT | 284434 |
rs778130022 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16772396 | CAGGCGCGGTGGCTC[A/G]TGCCTGTAATCCCAG | 284434 |
rs778164613 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16741478 | TCAAGCAATTCTCCT[G/T]CCTCAGCCTCCCAAG | 284434 |
rs778167505 | in-del | -/AGTTTCATTCTTGTTGCCCAGGCTTGCGTGCAATGGCAC | 1.64846e-05 | 0.0028709 | cds-indel, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800017 | TCTTTCAAGGTCTGG[lengthTooLong]GATCTCAGCGATGCT | 284434 |
rs778179787 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16804475 | TGGTACATGCCTGTA[A/G]TCCTAGTTACTCCAG | 284434 |
rs778237979 | snp | C/T | 1.64754e-05 | 0.00287009 | missense | NWD1 | GRCh38.p7 | 19:16797819 | AACATGAAGACATGG[C/T]GGAGACGGCTGTTTT | 284434 |
rs778253647 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16729251 | TGCCACAGCTGCATG[A/G]CCCTGTGTGACCGGA | 284434 |
rs778255360 | snp | A/G | 0.000140795 | 0.00838916 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744440 | TCATCGGTGATCAGT[A/G]CGGCCCCTGTCTGAT | 284434 |
rs778293043 | snp | A/G | 2.04021e-05 | 0.00319385 | intron-variant | NWD1 | GRCh38.p7 | 19:16762189 | CCTCCACCCTGCCTG[A/G]CATTGCTCACCTCCT | 284434 |
rs778312265 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16768055 | GGAGTGCAGTGGCAC[A/G]ATCTCAGCTCACCGC | 284434 |
rs778315696 | snp | A/T | 0.000161512 | 0.00898498 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744587 | CCACCTACGTCCTGC[A/T]GGCACCAGGTACTGG | 284434 |
rs778348843 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16723176 | GTAGCTAGGACCGCA[A/G]ACACGAATCACCATG | 284434 |
rs778367704 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16781062 | ATTTGTCGACCTCAG[A/G]TCCTAAGTAAGGTTG | 284434 |
rs778376303 | snp | C/T | 0.000773934 | 0.0196562 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744563 | AGAGGGACGAGAATG[C/T]GTTTCCTCCCACCTA | 284434 |
rs778396510 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16778498 | TTCTTCTTCTTCTTT[-/T]TTTTTTTTTTGTTGT | 284434 |
rs778396637 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16781651 | ATTTATTTGTTGACC[G/T]GAGATCTTATTACTA | 284434 |
rs778421704 | snp | A/C/T | 3.4458e-05 | 0.00415066 | missense, intron-variant | NWD1 | GRCh38.p7 | 19:16749846 | TATGGGCTGCCCTTG[A/C/T]CCCCTGCCCAGGTTC | 284434 |
rs778443869 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16794933 | ATTACAGGCACACAC[C/T]ACCACACCCAGCTAA | 284434 |
rs778476669 | snp | A/G | 0.00043262 | 0.0147011 | intron-variant, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16745039 | GAGGCTGGGTAATTT[A/G]CAAAGGAAAGAGGTT | 284434 |
rs778549596 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16736071 | TCTGGTGAAGAACCC[C/T]ATCCAGGGTACCCCA | 284434 |
rs778568082 | snp | A/G | 1.64953e-05 | 0.00287182 | missense | NWD1 | GRCh38.p7 | 19:16779456 | ATCCACATGCTAACT[A/G]GACACACAGGTGAGA | 284434 |
rs778599464 | snp | A/G | 1.74711e-05 | 0.00295554 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749146 | TTTGGCAGTCATTGA[A/G]TGGGAGATAGAGCGG | 284434 |
rs778608744 | snp | A/C | 3.30131e-05 | 0.00406269 | utr-variant-3-prime, synonymous-codon | NWD1 | GRCh38.p7 | 19:16815041 | AGGCACCCTGCTGAC[A/C]GTCCAGTTTGTCCAT | 284434 |
rs778611993 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16797329 | GTTCCAAAACATCTC[C/T]TTTTTTTTTTTTTTT | 284434 |
rs778627689 | in-del | -/CAC | 1.66059e-05 | 0.00288144 | cds-indel, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749478 | ATCACCAGGTCCTCA[-/CAC]GCCTCCGTGAGCTGG | 284434 |
rs778664202 | snp | C/T | | | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16717932 | ATCTCACTGCAGCCT[C/T]GACTTTCTGGGCTCA | 284434 |
rs778673621 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16723884 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 284434 |
rs778692848 | snp | C/T | 3.30044e-05 | 0.00406216 | intron-variant | NWD1 | GRCh38.p7 | 19:16788957 | TCCCAGCTAATATAC[C/T]CTCCCCTACCCTGGC | 284434 |
rs778693010 | snp | C/T | 1.65817e-05 | 0.00287933 | intron-variant | NWD1 | GRCh38.p7 | 19:16763809 | TGTCCAAGCTGCAGT[C/T]TCCCTTCTCCTCTGC | 284434 |
rs778696136 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16753300 | CCTAATTCCAAAGTA[C/T]AGGGAGACAGAAATC | 284434 |
rs778744141 | snp | G/T | 9.8912e-05 | 0.0070318 | | | GRCh38.p7 | 19:16763880 | CAAACCTGCGGAAGC[G/T]GAAGGAGTTGCCCTA | 284434 |
rs778745387 | in-del | -/TTTTTTG | | | | | GRCh38.p7 | 19:16718682 | ACCACGCCCAGCTAA[-/TTTTTTG]TTTTTTGTTTTTTGT | 284434 |
rs778757672 | snp | C/T | | | | | GRCh38.p7 | 19:16807985 | ACGAGTGTGCAACTT[C/T]CAAAGCGTTTCCCTT | 284434 |
rs778765790 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16808833 | GTGCAGTGGCTCACC[C/T]GGCACTTTGGGAGGC | 284434 |
rs778784510 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16724583 | CTGGACGTGGGGCCT[C/T]ACACCTGTAATATCA | 284434 |
rs778823432 | snp | A/G | 0.000181373 | 0.00952122 | missense | NWD1 | GRCh38.p7 | 19:16807804 | CTGGCCATCGCCTAT[A/G]ACAACATCGTCCTGG | 284434 |
rs778835753 | snp | A/G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754258 | CTCCATCTTCCATCC[A/G/T]TCTATCCATCATCTC | 284434 |
rs778838945 | in-del | -/TCCA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16753815 | CCCTCCCTCCCTCCC[-/TCCA]TCCATCATCTCTATC | 284434 |
rs778867325 | snp | A/G | 3.46669e-05 | 0.0041632 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749754 | CAGTGACCGTCCTGC[A/G]GCTGCTGGGGACGTC | 284434 |
rs778874354 | in-del | -/AAT | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748826 | AGACCCTGTCTCAAT[-/AAT]AATAATAATAATAAG | 284434 |
rs778927554 | in-del | -/ATGCTGTGGTAA | 1.64866e-05 | 0.00287106 | cds-indel | NWD1 | GRCh38.p7 | 19:16815055 | CAGTCCAGTTTGTCC[-/ATGCTGTGGTAA]ACAGAATCATCCCAA | 284434 |
rs778928217 | in-del | -/TCC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16764386 | CCATCCATCCATCCA[-/TCC]ATCCATCCATCCATC | 284434 |
rs778929268 | in-del | -/G | 1.64992e-05 | 0.00287216 | frameshift-variant, utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16797862 | CAACCTGATCATCAC[-/G]GGGTCCCTTGATGCG | 284434 |
rs778973967 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16771754 | GGACAACCATGTGCT[C/T]TCCGTACATCCAAGC | 284434 |
rs778996786 | snp | C/G | 1.65655e-05 | 0.00287793 | missense | NWD1 | GRCh38.p7 | 19:16791361 | TTAGATCAATGCTTG[C/G]AATCTGGAAACTGCA | 284434 |
rs779026196 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16778147 | ACGGGCTCTGATTCA[A/G]CACCACCCATTTTAC | 284434 |
rs779026868 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16773500 | TCTCTCTGCCCCACC[C/T]CAAGGGACTGTAGAT | 284434 |
rs779028401 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16763580 | GCTCAGTTCCGATGC[C/T]TCTGCCTTCAGGAAA | 284434 |
rs779049529 | snp | C/T | 1.64947e-05 | 0.00287177 | missense | NWD1 | GRCh38.p7 | 19:16765064 | TTTCCTGCCGGGGCA[C/T]CTCTGGGGGCATTGA | 284434 |
rs779057858 | snp | A/G | 1.65446e-05 | 0.00287612 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749325 | TTCTCAGCAGCCTCA[A/G]AAGTCACATCACTGA | 284434 |
rs779071199 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16804334 | GCCTGTAATCCCAGC[A/G]CTTTAGGAGGCTGAG | 284434 |
rs779090515 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16780776 | AATCCTCCCATCTCA[A/G]CCTCTTGAGTAGCTG | 284434 |
rs779104852 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16797538 | AATACATGAAACATC[A/G]GGGTTCACCATGTTG | 284434 |
rs779121246 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16726320 | CTCACTGTGTTGCCC[C/T]GGCTGGCCTTGAACT | 284434 |
rs779146966 | snp | A/G | 0.00024727 | 0.0111164 | missense, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800043 | ATGCTCATAGGTCCC[A/G]GGTGCCTGCACCATT | 284434 |
rs779216711 | snp | A/G | 0.000140696 | 0.0083862 | synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744462 | CTGTCTGATTCCCTC[A/G]CGGATCGATGAGAAG | 284434 |
rs779271725 | snp | C/T | 0.000164959 | 0.00908033 | missense, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800082 | GCACCGGCCTCACCG[C/T]AGTGTCCCACAATGG | 284434 |
rs779283291 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16793566 | TTAACTGTTTTTTTG[G/T]TTTTTGGTTTTTGGT | 284434 |
rs779286249 | snp | C/T | 2.14742e-05 | 0.00327668 | missense, intron-variant | NWD1 | GRCh38.p7 | 19:16794485 | CCAAAGGGGACAGAT[C/T]GCTGGAGAAGCTTCC | 284434 |
rs779324661 | snp | A/C | 1.64762e-05 | 0.00287016 | missense | NWD1 | GRCh38.p7 | 19:16791459 | AGGCCACACTGCTGA[A/C]AGTGTCCAGGGATGG | 284434 |
rs779372713 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16785670 | TCTATATTTTTGTGT[A/G]TGTATATATTTATGC | 284434 |
rs779387445 | snp | C/T | 3.30022e-05 | 0.00406202 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807789 | AAGTGCGAGGACCGC[C/T]TGGCCATCGCCTATG | 284434 |
rs779444495 | snp | A/G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16779691 | TGCCCAGGCTGGAGT[A/G/T]CAGTGGTGTGTTTAT | 284434 |
rs779448254 | snp | A/G | 3.336e-05 | 0.00408398 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749582 | ATTCAGACCTTCTGC[A/G]GACGCCAGGAACTCC | 284434 |
rs779449587 | snp | A/G | 4.95569e-05 | 0.00497755 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16762066 | CGACTTCTTCTCAGG[A/G]ACCTGGAGCCAGGGT | 284434 |
rs779449634 | snp | C/T | 1.64874e-05 | 0.00287113 | intron-variant | NWD1 | GRCh38.p7 | 19:16779326 | AGATCATTGCTGTTG[C/T]CTCTGTGTGGCTGCA | 284434 |
rs779463393 | snp | A/G | 1.73643e-05 | 0.0029465 | synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749680 | GCCCCCAGGCATTGG[A/G]AAGACAGCCCTGATG | 284434 |
rs779483530 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16761009 | CCTGTCCCCATCAGC[C/T]GTCACTCCTCATTCC | 284434 |
rs779505296 | snp | C/T | 1.7213e-05 | 0.00293364 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749655 | AGCACACCCCCCTGG[C/T]ACTCTTTGGGCCCCC | 284434 |
rs779515951 | snp | C/T | 6.75459e-05 | 0.00581106 | synonymous-codon, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749938 | AAACTTCGAGTCTCT[C/T]GTGCTCCTGCTGGAT | 284434 |
rs779538269 | snp | A/T | 1.64947e-05 | 0.00287177 | stop-gained | NWD1 | GRCh38.p7 | 19:16808088 | GGATGCCCTGCTGTG[A/T]CTCTGGGACCTGCAG | 284434 |
rs779545915 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16785831 | TATCAATGTTTTGCC[A/G]TAAACATTCTTTTGT | 284434 |
rs779559959 | snp | A/G | 1.64882e-05 | 0.00287121 | missense | NWD1 | GRCh38.p7 | 19:16759254 | AGGCGGAGCTGAAGG[A/G]TGTTTTGTCCCTGGA | 284434 |
rs779625065 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16798734 | TGGGTTCAAGCAATT[A/C]TCCTGCCTCAGCCTC | 284434 |
rs779651374 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16787128 | CTCTAAGATTATTAT[A/G]TTTATTTATTTATTT | 284434 |
rs779664264 | snp | A/C | 5.07361e-05 | 0.00503641 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16789184 | GTATTCAGCATCTGG[A/C]TCAAAGGTAACAAAC | 284434 |
rs779714233 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16767736 | AACATGTGGGGATTA[A/T]GGGGATTACAATTCA | 284434 |
rs779717052 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16727186 | CCCCGGGCCCCAATG[A/C]CCAGCACTGGGAAAC | 284434 |
rs779720780 | snp | C/T | 3.3095e-05 | 0.00406773 | missense, synonymous-codon | NWD1 | GRCh38.p7 | 19:16797749 | TTTGGAAGATCGGTG[C/T]GGATATTCTTGGCGG | 284434 |
rs779753939 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16799821 | CCCAATGGGCTGAAG[C/T]GTATTTCTGAACTAT | 284434 |
rs779800778 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16808764 | AGGCATGACCCACCG[C/G]ACCTGGCTACAAAGT | 284434 |
rs779827293 | snp | A/G | 0.000639386 | 0.0178685 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16744580 | TTTCCTCCCACCTAC[A/G]TCCTGCAGGCACCAG | 284434 |
rs779834170 | snp | A/G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16768393 | TTTGTTTATCCGTTC[A/G/T]TCTGTCTGTGGACAT | 284434 |
rs779847692 | snp | A/C | 1.64833e-05 | 0.00287078 | missense, downstream-variant-500B | NWD1 | GRCh38.p7 | 19:16800033 | GATCTCAGCGATGCT[A/C]ATAGGTCCCGGGTGC | 284434 |
rs779865059 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751520 | GAAGGAAGGAAAGAG[G/T]CCTGGCATGGTGGCT | 284434 |
rs779877857 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16725188 | CCAGCTAATTTTTGT[A/G]TTTTTAGTAGAAGCA | 284434 |
rs779900638 | snp | C/T | 1.64822e-05 | 0.00287068 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16779437 | CATGGAAGAGCAGCA[C/T]GTGATCCACATGCTA | 284434 |
rs779934306 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16798821 | TAGTAGAGACGGGGT[C/T]CCGCCATGTTGGCCA | 284434 |
rs779952892 | snp | A/G | 1.65102e-05 | 0.00287312 | missense | NWD1 | GRCh38.p7 | 19:16765039 | TCTCCCTCAGGCAGC[A/G]TGAGCTGGATTTCCT | 284434 |
rs779956067 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16736844 | GAGGGAAGTAGGTAC[C/T]GTTTCTGCTTTCGTA | 284434 |
rs779962217 | snp | A/G | 1.67916e-05 | 0.0028975 | utr-variant-3-prime, missense | NWD1 | GRCh38.p7 | 19:16815280 | CAGAAAGTGCCCAGG[A/G]AAATGAAACCAAATC | 284434 |
rs779963790 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16723807 | TTCAAGCGATTCTCG[G/T]GTCTGAGCCCCCCAC | 284434 |
rs779967735 | snp | A/C | 1.64912e-05 | 0.00287147 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16749254 | CCTTGAAGACTGCGC[A/C]CTTAGGATGGTGGAC | 284434 |
rs779967968 | snp | A/T | 1.66474e-05 | 0.00288503 | missense | NWD1 | GRCh38.p7 | 19:16750093 | TGCAGCGGGTGCTCC[A/T]GGACCCGGAGGCCTA | 284434 |
rs779987903 | in-del | -/T | 6.64628e-05 | 0.00576429 | intron-variant | NWD1 | GRCh38.p7 | 19:16765021 | CCACATCCTCCCCCC[-/T]TCTCTCCCTCAGGCA | 284434 |
rs780003997 | snp | A/G | 1.65707e-05 | 0.00287838 | missense | NWD1 | GRCh38.p7 | 19:16765141 | CCTGAGGTTGGCCTG[A/G]TCCGTGAAGCCCTCC | 284434 |
rs780018372 | snp | A/T | 1.7219e-05 | 0.00293414 | intron-variant | NWD1 | GRCh38.p7 | 19:16750451 | TTATTTATTTATTTA[A/T]GTTTTCTTTTTTTAT | 284434 |
rs780024373 | snp | C/T | 6.88018e-05 | 0.00586483 | missense | NWD1 | GRCh38.p7 | 19:16773296 | CCGGGAGGACCCCTC[C/T]GGGCAACTCTCAGCG | 284434 |
rs780025068 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16779564 | TCTGTATTGAAACCC[C/T]GGCCTTTGTTCCTGC | 284434 |
rs780041256 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16731580 | AAAATGCTGGGATTA[C/T]AGGCGTGAGCCACTG | 284434 |
rs780075830 | snp | A/G | 0.000139616 | 0.00835395 | missense, utr-variant-5-prime | NWD1 | GRCh38.p7 | 19:16731264 | TTCTGCCAGAGGCAC[A/G]GCTTGATGTTTGAGG | 284434 |
rs780094612 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754187 | TCTATCCATCATCTC[A/G]ATCTTCCATCCTTCC | 284434 |
rs780106918 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16783631 | AAGAGCAAAACTCCA[C/T]CTCAAAAAATAAAAA | 284434 |
rs780143274 | snp | A/T | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816019 | AGCCTTCTGTCCCAT[A/T]CCTGTTAGACCTCAC | 284434 |
rs780170961 | snp | A/T | | | missense | NWD1 | GRCh38.p7 | 19:16788997 | GAGAGGTGAGGTGTG[A/T]GAAAATATTTGCCAA | 284434 |
rs780171267 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16744396 | AAAAAAGTGAGATTT[C/G]AATCTGTGACTTCCT | 284434 |
rs780187684 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16743783 | CCTCTCCCGGGTTCA[A/G]GCAATTCTCCTGCCT | 284434 |
rs780194164 | snp | A/T | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16816370 | CATTTGGCATGTGCG[A/T]CTTTGGTTAATGAGC | 284434 |
rs780196666 | in-del | -/AAA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732218 | TGAGACTCCGTCTCA[-/AAA]AAAAAAAAAAAAAAG | 284434 |
rs780197985 | in-del | -/TC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16773857 | ATCCATTCATTCATC[-/TC]TCTATCTACCTCCCA | 284434 |
rs780263554 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16739729 | AATAAGTCATTAGGC[A/C]GCACCGAGGCCGGGG | 284434 |
rs780278786 | snp | G/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16796046 | GGATGTGAAGGTTGG[G/T]TCATCTCTCTCAGTG | 284434 |
rs780295828 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16720513 | GACTAGGGGGTTCTC[A/G]AGTAAGGGGAATTCT | 284434 |
rs780302686 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16775435 | CTCTTTCAGTCTGGC[A/G]CTCTGCCATTTTCAG | 284434 |
rs780318414 | snp | C/T | 1.68969e-05 | 0.00290657 | missense | NWD1 | GRCh38.p7 | 19:16750282 | AAGCCCGGAAATGGG[C/T]CTCTTTCACCGTGCC | 284434 |
rs780334014 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16778681 | GCCTGGCTAATTTTT[A/G]TATTTTTAGTAGAGA | 284434 |
rs780371424 | snp | A/G | 3.32121e-05 | 0.00407492 | synonymous-codon, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749500 | CCGTGAGCTGGATAC[A/G]GCCGGACAGGAGTTG | 284434 |
rs780381926 | in-del | -/TATT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16743654 | AAAAGAAACCATACA[-/TATT]TATTTATTTATTTAT | 284434 |
rs780395558 | snp | A/G | 5.00238e-05 | 0.00500094 | intron-variant | NWD1 | GRCh38.p7 | 19:16808148 | CACGGTGGGTGGCCC[A/G]CCTCCCCATGTTCAT | 284434 |
rs780404767 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16761065 | CATCTGCTTCCTGTC[A/T]CTGTGGATTTGCCTG | 284434 |
rs780407394 | snp | A/T | 1.76924e-05 | 0.0029742 | stop-gained | NWD1 | GRCh38.p7 | 19:16807651 | GTTGCTGAGCAGCGC[A/T]AGCTCCTATTTACGG | 284434 |
rs780539784 | snp | C/T | 1.71469e-05 | 0.002928 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16750334 | AGAGGAAGCCACGCA[C/T]CAACTCTGCACCCGC | 284434 |
rs780587163 | snp | A/G | 8.68923e-05 | 0.0065908 | missense, intron-variant | NWD1 | GRCh38.p7 | 19:16794550 | GAGTCCCTCCTCGCC[A/G]CAGGTAGCGTTTAGC | 284434 |
rs780613434 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16771715 | GAGGTGTAGGAACAA[A/G]TGTTATCACCAGAGG | 284434 |
rs780644137 | in-del | -/CCTC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782976 | CTCCCTTCTTTCCTT[-/CCTC]CCTCCCTCCCTCCTT | 284434 |
rs780656197 | snp | A/G | 0.000215841 | 0.0103862 | missense | NWD1 | GRCh38.p7 | 19:16773239 | TGGTTCCAGTTGTGC[A/G]CACACCCTGTGCTGG | 284434 |
rs780657067 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16759769 | GGAGGCTGAGGTGGC[A/G]GATCACCTGAGGTCA | 284434 |
rs780666332 | snp | C/T | 1.66518e-05 | 0.00288542 | missense, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16749574 | CGGAGGTCATTCAGA[C/T]CTTCTGCGGACGCCA | 284434 |
rs780746726 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16767610 | CAGAGTGAGACTGTG[C/T]CTCCAATAAAACCCA | 284434 |
rs780757117 | in-del | -/TTTTTTTTTTT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16767174 | GAGGTGCGTCTTTTT[-/TTTTTTTTTTT]TTTTTTTTTTTGGTG | 284434 |
rs780780047 | snp | A/G | 1.66236e-05 | 0.00288297 | utr-variant-3-prime, missense | NWD1 | GRCh38.p7 | 19:16815261 | GCTCCCCAGGACTTG[A/G]AGTCAGAAAGTGCCC | 284434 |
rs780786033 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16798529 | GGTGGGAGGATCACA[C/T]GAGCCTGGGAGGTAG | 284434 |
rs780830235 | snp | C/T | 4.06868e-05 | 0.00451018 | intron-variant | NWD1 | GRCh38.p7 | 19:16750420 | CTTCCCGGTAAGTCT[C/T]TGTGTTTTGAAACTC | 284434 |
rs780866855 | snp | A/T | 5.52776e-05 | 0.00525697 | intron-variant | NWD1 | GRCh38.p7 | 19:16794601 | AAGCTAATCAGGATC[A/T]GGTTGGAGAAGGGGG | 284434 |
rs780915526 | in-del | -/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16725487 | TGTATCACCTAACAA[-/C]AAACCTCCTGCAGGC | 284434 |
rs780928741 | snp | A/C | 1.67739e-05 | 0.00289597 | intron-variant | NWD1 | GRCh38.p7 | 19:16797919 | ACCCTTCATCCTCAC[A/C]TCCACCTCGGGAACA | 284434 |
rs780939014 | in-del | -/C | 1.73057e-05 | 0.00294152 | frameshift-variant, intron-variant | NWD1 | GRCh38.p7 | 19:16749824 | CTGCTTCCAGGTGTG[-/C]CTGGCCTATGGGCTG | 284434 |
rs780980424 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16811457 | GGCATGGTGGTGCAT[A/G]CCTGTAATCCCAGCT | 284434 |
rs780981698 | snp | A/G | 1.66916e-05 | 0.00288886 | missense, utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16799937 | ATCCTGGAAGGCGTC[A/G]GGGCCCCCGTGAGCC | 284434 |
rs781001126 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16756193 | GGAGGCGGAGGTTGC[A/G]GTGAGCCTAGATCAC | 284434 |
rs781003819 | snp | C/T | 1.64808e-05 | 0.00287057 | missense | NWD1 | GRCh38.p7 | 19:16808057 | ACAAGGAGCAGCTGG[C/T]GGTCAGCGGGTCTGA | 284434 |
rs781008894 | snp | A/G | | | synonymous-codon, intron-variant | NWD1 | GRCh38.p7 | 19:16749836 | GTGCCTGGCCTATGG[A/G]CTGCCCTTGCCCCCT | 284434 |
rs781029383 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16810373 | AACCTGGAAGGCAGA[A/G]GCTGCAGTGAGCCGA | 284434 |
rs781030743 | in-del | -/T | 1.88697e-05 | 0.00307156 | intron-variant | NWD1 | GRCh38.p7 | 19:16762176 | TCCCCACCTGCAACC[-/T]CCACCCTGCCTGGCA | 284434 |
rs781093948 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16774755 | CAACCCTTTCTTTCT[C/T]CCTTCCTTCCTCTCT | 284434 |
rs781095051 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16793951 | GGCTGCAATGCAGTG[A/G]CACAATCATAGCTCA | 284434 |
rs781104485 | snp | A/G | 1.64841e-05 | 0.00287085 | stop-gained | NWD1 | GRCh38.p7 | 19:16789135 | CTGAACCTCAGATCT[A/G]GAACCTTCATGTGGA | 284434 |
rs781111941 | snp | A/C | | | intron-variant, upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16748854 | AAGAAGAAGAATAAG[A/C]GTAATGGCTTAACTA | 284434 |
rs781133880 | snp | C/T | 2.75024e-05 | 0.00370816 | intron-variant | NWD1 | GRCh38.p7 | 19:16794433 | CTTAACCCGTGGAAG[C/T]GCCTGACAGGCATCC | 284434 |
rs781155293 | snp | C/T | 1.67189e-05 | 0.00289122 | intron-variant | NWD1 | GRCh38.p7 | 19:16791313 | TGTAGTCTAGGTCTC[C/T]TGCCAAGATGCTGCT | 284434 |
rs781164746 | snp | C/T | 1.68369e-05 | 0.0029014 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16749965 | GGATGCTATGGATGA[C/T]CTGGACTCTGTCCGC | 284434 |
rs781219768 | snp | C/G | 1.67122e-05 | 0.00289064 | missense | NWD1 | GRCh38.p7 | 19:16750038 | AGGGTGCACCTCATC[C/G]TCTCAGCTTGCTCGG | 284434 |
rs781251160 | snp | C/T | 0.000148267 | 0.00860879 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16807971 | GGACCTCTTTCTTTA[C/T]GAGTGTGCAACTTCC | 284434 |
rs781254177 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16760264 | TATTTTATTTTATTT[-/T]ATTTTATTTTATGTA | 284434 |
rs781263109 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16795142 | AAGCTGGGAGCAGGG[A/G]GCACCCCATTTATTC | 284434 |
rs781285548 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16745478 | GCCTACCTGTAATCC[C/T]AGAATTTTGGAAGGC | 284434 |
rs781299366 | snp | C/T | 6.58924e-05 | 0.0057395 | utr-variant-3-prime, missense | NWD1 | GRCh38.p7 | 19:16815157 | GCCTTTCAGCAAAAG[C/T]CTCACCGCAGGACCC | 284434 |
rs781315143 | snp | A/G | | | missense | NWD1 | GRCh38.p7 | 19:16807588 | TCTTCCCTGGCAGGC[A/G]AGGAACAAGATTCCC | 284434 |
rs781338802 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16763348 | TCTTGAGCCTGACCT[A/C]CCCAGCCTGATATTC | 284434 |
rs781360236 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16781864 | TTGGGAGGCCTAGGC[A/G]GGTGGATCACAAGGT | 284434 |
rs781370278 | in-del | -/CT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751048 | CAAAACATGGAGAAA[-/CT]CTGTCTCCACTAAAA | 284434 |
rs781377023 | in-del | -/A | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16817598 | AGAGACTCTGTCTCC[-/A]AAAAAAAAAAAAAAA | 284434 |
rs781396239 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16762739 | GGAGGCAGGACCAGG[C/T]TCTATTCTTTTTTTG | 284434 |
rs781412874 | in-del | -/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732599 | TCCCTGGCTAGGGAA[-/T]TTTTTTTTTTTTTTT | 284434 |
rs781439671 | snp | A/T | 3.32618e-05 | 0.00407797 | intron-variant | NWD1 | GRCh38.p7 | 19:16763790 | GAGTGAATGAATGGG[A/T]TTGTGTCCAAGCTGC | 284434 |
rs781465762 | snp | C/G | 1.64754e-05 | 0.00287009 | intron-variant | NWD1 | GRCh38.p7 | 19:16812853 | AGTGTGCTGGATGGT[C/G]AGTCATTTTGCTTTT | 284434 |
rs781474473 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16758597 | ATCCTAATTTAAAGA[C/T]AAGCCTTGGTGGGCC | 284434 |
rs781517913 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16722980 | CTGGCCATACAACTT[C/T]ACTGGGAGGGGACGA | 284434 |
rs781522475 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16793903 | TTTTAATTTAAAAAA[A/T]TTTTTAGAGACAGAG | 284434 |
rs781535797 | snp | C/T | | | utr-variant-3-prime | NWD1 | GRCh38.p7 | 19:16815914 | GCAGGAGTTTCTGTA[C/T]CTATTTTACAGATGA | 284434 |
rs781552364 | snp | C/G | 9.49803e-05 | 0.00689066 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16759384 | GGGATACTACTTGGC[C/G]CGGCGGCCCGTGGAT | 284434 |
rs781652922 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16801378 | TGGGAAGTTGAGGCT[A/G]CAGTGAGTCATGATC | 284434 |
rs781681267 | snp | C/T | 1.64863e-05 | 0.00287104 | synonymous-codon | NWD1 | GRCh38.p7 | 19:16763869 | ACATACGGTTGCAAA[C/T]CTGCGGAAGCTGAAG | 284434 |
rs781698174 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16729986 | TAGCCCAGCCCACCC[A/G]TGTGTTTTCAATAGC | 284434 |
rs781700846 | snp | C/T | | | upstream-variant-2KB | NWD1 | GRCh38.p7 | 19:16718057 | ATGAGGGTCTCACTA[C/T]GTTGCCCAGGCTGGT | 284434 |
rs781740345 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16814907 | GGCATAATAAATGTC[A/G]TGCCAAAATTAGTAG | 284434 |
rs781761745 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16802811 | TTCGAGACTAGCCTG[A/G]CCAACATGGTAAAAC | 284434 |
rs796093683 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16802555 | CCCCAACCCCCTTCA[C/T]CTTTTGTATTAAGAA | 284434 |
rs796103930 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16802663 | TAAACCTCTTATTCA[C/T]AATTATGCATTACTG | 284434 |
rs796108989 | in-del | -/AA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16733521 | ATGAGATTCTGTCTC[-/AA]AAAAAAAAAAAAAAT | 284434 |
rs796116538 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16779108 | ACTTATGACCACACT[A/G]TGATGCAGTCCCCTT | 284434 |
rs796126962 | in-del | -/AT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790641 | TAACATTAAAAAAAA[-/AT]AAATAAATAAATAAA | 284434 |
rs796132875 | in-del | -/TTTTTCTTTTTT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16809554 | TTTTTTTTCTTTTTC[-/TTTTTCTTTTTT]TTTTTTTGAGATGGA | 284434 |
rs796135143 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16723798 | CCTCCTTGGTTCAAG[C/G]GATTCTCGTGTCTGA | 284434 |
rs796147074 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16778500 | CTTCTTCTTCTTTTT[C/T]TTTTTTTTGTTGTTG | 284434 |
rs796162567 | multinucleotide-polymorphism | CA/TG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16778791 | GCCTCCCAAAGTATT[CA/TG]CCTCCCACAGTGCTG | 284434 |
rs796164179 | in-del | -/AAGG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751482 | AGAGAAAGAAAGAGA[-/AAGG]AAGGAAGGAAGGAAG | 284434 |
rs796176119 | in-del | AAAA/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16728957 | CAAAAAAAAAAAAAA[AAAA/T]AAATAAGTAATTGCA | 284434 |
rs796231918 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16731675 | AATGGTGCAATCTCA[A/G]CTCACTGCAACCTTG | 284434 |
rs796246638 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16733536 | AAAAAAAAAAAAAAA[-/A]TCAAGTGGCTCTTTG | 284434 |
rs796255727 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16747289 | ATCGGCCCGCCTTGG[A/C]CTCCCAAAGTGCTGG | 284434 |
rs796344291 | in-del | -/CCTA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16736224 | TTTCCTTCCTTCCTT[-/CCTA]CCTTCCTCTCTCTCT | 284434 |
rs796370105 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16793998 | CTAGGGGCACAAGTG[A/T]TCCTCCTGCTTGAGC | 284434 |
rs796370392 | in-del | AAA/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16728958 | AAAAAAAAAAAAAAA[AAA/T]AAATAAGTAATTGCA | 284434 |
rs796403989 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16806705 | AACAGAGTGAGACTC[C/T]GTCTCTTAATAAATA | 284434 |
rs796404888 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16776774 | CCTCTACAAAAAGTT[A/T]AAAAAAAAAAAAAAA | 284434 |
rs796406733 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16799479 | GATTACAGGTGTGAG[C/G]CACTGCACCTGGCCT | 284434 |
rs796441427 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16796701 | TTCCTCTTTACTTTT[C/T]TTCCTCTCTACCTCC | 284434 |
rs796475761 | in-del | -/GTTTT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16766559 | GTTCTGTTTGGTTTT[-/GTTTT]AATTATAGCAAAATA | 284434 |
rs796477784 | in-del | -/GAAG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751818 | AAAGAAAGAGAAAGA[-/GAAG]GAAGGAAGGAAGGAA | 284434 |
rs796499787 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16758791 | GAGGCAGGTGGATCA[C/G]GAGGTCAGGAGTTGG | 284434 |
rs796507541 | multinucleotide-polymorphism | CA/TG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16722255 | GTGAGCCACAATAGT[CA/TG]CACTGCACTCCAGCC | 284434 |
rs796518952 | in-del | -/AAAAGT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732672 | AAAAAAAAAAAAAGA[-/AAAAGT]GAAAAAGTGCAGTGG | 284434 |
rs796521415 | in-del | CG/TGAAA | | | intron-variant | NWD1 | GRCh38.p7 | 19:16722114 | GAGACCCTGTCTCTT[CG/TGAAA]AAACAACAACAACAA | 284434 |
rs796528092 | snp | A/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790874 | AAGGTAGCTAATGAG[A/T]TTAAAATCACATGTG | 284434 |
rs796532520 | snp | C/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16727607 | CGGCTTCTGCGGGGT[C/G]AAGCCGGCCCCCTCC | 284434 |
rs796540481 | in-del | -/AC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16746692 | AAAAAACAAAAAACA[-/AC]AAAAAAAAACAGTCG | 284434 |
rs796554678 | in-del | G/TTTCCTTCC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16736193 | TCCTTCTTTCCTTCT[G/TTTCCTTCC]TCCTTCTTTCCTTCC | 284434 |
rs796560835 | in-del | AAA/GT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732676 | AAAAAAAAGAAAAAG[AAA/GT]AAAAAGTGCAGTGGT | 284434 |
rs796576987 | in-del | -/AAG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16751861 | TAAGAAAGAAAAAAA[-/AAG]AAGGAAAGAAGAGAT | 284434 |
rs796592823 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16805184 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGAGATTAC | 284434 |
rs796623732 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16759940 | CAGAGGTGGCAGTGA[A/G]CCAAGATCGCACCAC | 284434 |
rs796636657 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16756024 | GAACATGTATTTCAT[A/G]TGTTCTATGTATTAC | 284434 |
rs796644791 | in-del | -/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16733804 | CATCGGGAGACGGCG[-/G]TCCCTCCAGAAGCAC | 284434 |
rs796666641 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16729883 | AAAAAATAAAAAAAG[A/G]GAAAAGAAAAGAAAG | 284434 |
rs796688183 | multinucleotide-polymorphism | AA/TT | | | intron-variant | NWD1 | GRCh38.p7 | 19:16742847 | GCTATTTTTAAAAAA[AA/TT]TTTTTGTAGAGACAG | 284434 |
rs796692944 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16738554 | AGACTGCGCAACAGA[C/T]GGAGACTCTGTCAAA | 284434 |
rs796702725 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16761805 | TAAATTGATGTAAGG[-/A]AAAAAAAAACACGGA | 284434 |
rs796723218 | in-del | -/TTCC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16783021 | TCTTTCTTTCCTTCT[-/TTCC]TTCTTTCTTTTCTTT | 284434 |
rs796729484 | in-del | -/AAAAAAAAAAAAG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16732658 | GACTTCATCTCAAAA[-/AAAAAAAAAAAAG]AAAAAAAAAAAGAAA | 284434 |
rs796737263 | in-del | -/AG | | | intron-variant | NWD1 | GRCh38.p7 | 19:16738003 | AGAAAAGAAAAGAAA[-/AG]AGAAAAGAAATTCTA | 284434 |
rs796770819 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16789494 | TAAATTTTGACGTGT[A/G]TTTTCATTTACATTC | 284434 |
rs796787737 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16755839 | CACCGTACCTGGCCT[A/G]TAATCTATCTCTGTA | 284434 |
rs796790561 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16761553 | TTTTTAGTACAGACA[A/G]GGTTTCACCACGTTG | 284434 |
rs796797607 | snp | C/T | | | intron-variant | NWD1 | GRCh38.p7 | 19:16730915 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTTGA | 284434 |
rs796836357 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16790378 | AAGTAATTGGTGGTT[A/G]TTGACAGTAATATCA | 284434 |
rs796837879 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16810224 | GGGTGGATCACCTGA[A/G]GTTAGGGGTTCGAGA | 284434 |
rs796841379 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16811572 | CAGGGCAACAAGAGC[A/G]AGACTCTGTCTCAGA | 284434 |
rs796842807 | snp | A/C | | | intron-variant | NWD1 | GRCh38.p7 | 19:16809066 | TCTCAAGAAAACAAA[A/C]AACAAAAACTCAGCA | 284434 |
rs796915845 | in-del | -/A | | | intron-variant | NWD1 | GRCh38.p7 | 19:16797180 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAT | 284434 |
rs796925609 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16782688 | TCTATAGATTCAACC[A/G]ACTGTGGATTGAAAA | 284434 |
rs796939375 | in-del | -/CATC | | | intron-variant | NWD1 | GRCh38.p7 | 19:16754791 | ACCTATCATCTCTAT[-/CATC]CATCCATCCATCCAT | 284434 |
rs796949285 | in-del | -/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16737965 | GCAAGACTCTATCTC[-/G]AAAAGAAAAGAAAAG | 284434 |
rs796971315 | snp | A/G | | | intron-variant | NWD1 | GRCh38.p7 | 19:16767828 | CAGTCCCTGGCAACC[A/G]CCATGCTATTTTCTG | 284434 |