SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs145526243 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | YES1 | GRCh38.p7 | 18:738677 | CCTGGGTGACAGAGC[A/G]AGACTCCCATCTCAA | 7525 |
rs145535884 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:790606 | ATGAGAAGGGTACTA[A/G]AGCCACAGATGATTT | 7525 |
rs145544041 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:783185 | GCCCAGGAATTTGAG[C/T]CTGCCTGGGCAAAAT | 7525 |
rs145578463 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | YES1 | GRCh38.p7 | 18:725870 | GCCTGGGTGACAGAG[C/T]GAGACTCCATCTCGC | 7525 |
rs145619809 | snp | C/G/T | 0.000183083 | 0.00956609 | synonymous-codon | YES1 | GRCh38.p7 | 18:742973 | AGAAACAACAGCATA[C/G/T]AGTGGAACAAGTTTA | 7525 |
rs145620413 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | YES1 | GRCh38.p7 | 18:766179 | CCTATCCAGCCCTAC[A/G]TAGTAAATATTGATT | 7525 |
rs145694809 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:727877 | TCTGAGGAAAAGTTA[C/G]CTGTCTGACTGTTGT | 7525 |
rs145694861 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | YES1 | GRCh38.p7 | 18:771304 | CCTAGGAGGCGGAGG[C/T]TGCAGTGAGCCAAGA | 7525 |
rs145760770 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:737105 | GGTATAGTCTAGAAG[A/G]TAACAGGAAAACCAG | 7525 |
rs145836635 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | YES1 | GRCh38.p7 | 18:731760 | ATCACAAGGTCAGGA[A/G]ATCGAGACCATCCTG | 7525 |
rs145855201 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:807178 | GTCTCTACTAAAAGT[A/G]CAAAAATTAGCCGGG | 7525 |
rs145916337 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:735319 | GTATACTACTCAGCC[A/G]TAAAAAGGAATGAAA | 7525 |
rs145919143 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | YES1 | GRCh38.p7 | 18:809448 | GGGATTACAGGGGCG[C/T]GCCACCACACCCAGA | 7525 |
rs145929073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:740745 | ATTCTAAATCTCTCC[C/T]GCCTGGAAATAATTG | 7525 |
rs145947377 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:735699 | AGCCTGGGCTGGGCA[A/G]CAGAGTGAGACTCCG | 7525 |
rs146030357 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:797282 | ATAATTTTAAGATAT[A/C]TTTATTCATATATAT | 7525 |
rs146051750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:759138 | ACTCTCTTAAATTGG[C/T]ATATTCTAAAGATGT | 7525 |
rs146073176 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:800857 | ATCTCTGGAAAAAAT[A/T]AAAACAAAGGCTGGG | 7525 |
rs146110250 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:810273 | TCTAGTCTTTTAGCA[C/T]ATTTATTCTTTTATC | 7525 |
rs146138113 | in-del | -/GCG | | | intron-variant | YES1 | GRCh38.p7 | 18:812017 | CGGGGGCGGGGAACC[-/GCG]GCGGCGGCGGCGGCG | 7525 |
rs146163966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:738716 | AAAAAAAAAAAATTC[A/G]GCATACACTTTAGAT | 7525 |
rs146191790 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:745149 | TTTCAGGTGCATTCA[C/T]ATGCCAAATTGGTAA | 7525 |
rs146226517 | in-del | -/GT | 0.0547245 | 0.156101 | intron-variant | YES1 | GRCh38.p7 | 18:735573 | ACAAAAATTAGCTGG[-/GT]GTGGTGGTACGAGCC | 7525 |
rs146279936 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:764216 | TTGGCTGACTCCAAA[A/G]GTTTCCAGTTTTTTA | 7525 |
rs146292164 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:725515 | CTATTAAAAAAAACT[C/T]TACATGACATTACTT | 7525 |
rs146312589 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722900 | GATCGAGACTATCCT[A/G]GCTAACACGGTGAAA | 7525 |
rs146390244 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776528 | TTCTATAGGGTTGTC[G/T]GTCCTTTTCTTATTG | 7525 |
rs146446429 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | YES1 | GRCh38.p7 | 18:784375 | GCTGGAGACGTTAAA[C/T]AGGTTTTGGTTCTAT | 7525 |
rs146475145 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:793607 | CTCCCAAAGCACTGG[C/G]ATTACAGGTGTGAGC | 7525 |
rs146477038 | snp | A/G | 0.0225045 | 0.103662 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723038 | CAGAGCTTGCAGTGA[A/G]CCGAGATCGCGCCAC | 7525 |
rs146490053 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:789248 | AATATTCATGACCCA[A/G]TACACTTATGTCAAA | 7525 |
rs146494327 | snp | A/C | 0.0178098 | 0.0926698 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:721910 | AACTTCCACATTAAG[A/C]CACTGAAGACGAAAA | 7525 |
rs146572824 | snp | A/C/G | 0.00279242 | 0.0372774 | intron-variant | YES1 | GRCh38.p7 | 18:803727 | AAGGTGGGAAAGGAG[A/C/G]GTGACTGGCAAGGCT | 7525 |
rs146593911 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:736236 | TGGAGGTAACTGTAC[A/G]GAAGTATGGAGGTTG | 7525 |
rs146614101 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:807747 | TTCAGGCAGCCACCA[C/G]GGATATGCAATGTAT | 7525 |
rs146615920 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | YES1 | GRCh38.p7 | 18:734707 | AAAAAAACAATAGAT[A/G]TTGGTGTGGATGTGG | 7525 |
rs146633417 | snp | A/C | 6.80944e-05 | 0.0058346 | missense | YES1 | GRCh38.p7 | 18:739780 | CTTCAAATACTTTCC[A/C]TCTCCTTCCTTAAGG | 7525 |
rs146712255 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | YES1 | GRCh38.p7 | 18:757232 | AGTATCGCTGGGCGC[A/G]GTGGCTCACGCCTGT | 7525 |
rs146730658 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | YES1 | GRCh38.p7 | 18:753071 | AGCCAAACTATTATT[C/T]GCAAACAAAACAAAT | 7525 |
rs146799063 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:734405 | TAAAAATACAAAAAA[A/T]AAAATTAGCCGAGCT | 7525 |
rs146809128 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:810983 | GATTTACCATGCACT[G/T]TTCCTTAAATGCACA | 7525 |
rs146829803 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | YES1 | GRCh38.p7 | 18:808829 | AACTCCAACACCATA[C/T]TGTCATTTGCCTTTT | 7525 |
rs146833025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:773555 | AAGGCTGGTAAGACA[A/G]TGAGGAAAGACAGAC | 7525 |
rs146852101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:771209 | TCGTCTCTACTAAAA[A/G]TACAAAAATAAGCTG | 7525 |
rs146904811 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | YES1 | GRCh38.p7 | 18:757940 | TCATAAGGTTTACTA[C/T]GAGGATTAACTTTAT | 7525 |
rs146943900 | snp | A/G | 0.0337553 | 0.125452 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722816 | AGTGAATGTAGGCTG[A/G]GCGCGGTGGCTCACG | 7525 |
rs146966353 | in-del | -/G | 0.253264 | 0.249979 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722366 | GCATGAAGTCCATCT[-/G]TCACATTTTAAAAAT | 7525 |
rs146976732 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:772556 | TCCTGCCTCAGCCTC[C/T]TGAGTAGCTGGGATT | 7525 |
rs146993103 | snp | A/C | 0.00199481 | 0.0315187 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813121 | TCTATATGATGCTGG[A/C]GGCAGCCCAGTGAGG | 7525 |
rs147032357 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | YES1 | GRCh38.p7 | 18:737962 | TTATAGGAGCCATCT[C/T]GCACAGCCTGGTTTT | 7525 |
rs147081257 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | YES1 | GRCh38.p7 | 18:791884 | ACATGGTGAAACCCC[A/G]CCTCTACTAAAAATA | 7525 |
rs147116037 | snp | A/G | 0.00368486 | 0.0427651 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724385 | ACACAAGTTCTTTAT[A/G]TTTTGGCAGATTTGT | 7525 |
rs147116326 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | YES1 | GRCh38.p7 | 18:795000 | TTTGTATTTTTAGTA[C/T]AGACAAGGTTTCACC | 7525 |
rs147164422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:730448 | TTCCTGGGCTCAAGC[A/G]ATCCACCCACCTTAG | 7525 |
rs147200238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:733441 | TCAAATACTTACTGT[A/G]TATCTTTTTTGTGGA | 7525 |
rs147200848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:805734 | AAAGTATCCTTATCT[A/G]TAAAATATTAATCAC | 7525 |
rs147228514 | snp | A/G | 0.000131791 | 0.00811655 | missense | YES1 | GRCh38.p7 | 18:756584 | CAGGATATGAACTTG[A/G]CACCACTGAAAATGA | 7525 |
rs147232693 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | YES1 | GRCh38.p7 | 18:787642 | TTTAACCTGGGATGC[A/G]GAGGTTGCAGTGAGC | 7525 |
rs147269842 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:792318 | CGAAAAACAAACAAA[A/C]AAATAAATAAAGAAG | 7525 |
rs147269981 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:746167 | GAATAGCTAGAGAAC[A/T]TGGCTCAAAATACAG | 7525 |
rs147339862 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | YES1 | GRCh38.p7 | 18:806399 | TCACCTTCTAGAACA[A/G]AACCTTGAGAGCAAA | 7525 |
rs147376338 | snp | A/G | 0.252983 | 0.249982 | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721309 | TTGGGAGGCCGAAGC[A/G]GACGGATCACGAGGT | 7525 |
rs147378126 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:809586 | GATTACAGGTGTGAG[C/G]CACCGTGCCCAGCCT | 7525 |
rs147414552 | snp | C/T | 0.139564 | 0.224285 | intron-variant | YES1 | GRCh38.p7 | 18:767769 | ACAGGGGCACGATCT[C/T]GGTTCACTGCAACCT | 7525 |
rs147468788 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:751936 | CAGAAACTATTTTTA[A/G]AAGTTGGAACTACTG | 7525 |
rs147482667 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:781639 | TGATGCCCAATGAAT[A/G]TTTTTACAGATCATG | 7525 |
rs147519418 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:786009 | ACCATGAGATAACAC[A/G]GCAAGAAGAAGGCCC | 7525 |
rs147550647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:726440 | AAAAACACAAAAACA[A/G]AAACAACTTCACTCT | 7525 |
rs147566914 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:765014 | GCTGAGATTACAGGC[A/G]TGAGCCACCTCGCCC | 7525 |
rs147567387 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723130 | AATGTAGATTCAAAC[A/G]TGATTTGAAAACTGG | 7525 |
rs147635898 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:778154 | CTGAAATGGAGAGAG[A/G]TTATTACATGCCTTG | 7525 |
rs147655425 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | YES1 | GRCh38.p7 | 18:741789 | GGATAGAGTGAGGCC[C/T]CACCTCACAAAAAAA | 7525 |
rs147671603 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:738217 | GGCTAGGAGGTAAGA[G/T]TCCAAAACCAGCATG | 7525 |
rs147671864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:782163 | TTATCTTAGTCTCTC[C/T]TCATCTTTCATCTTT | 7525 |
rs147739615 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | YES1 | GRCh38.p7 | 18:798617 | TTCTTTGATATGGCT[A/G]ATTAGTATCTGTTCT | 7525 |
rs147774899 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | YES1 | GRCh38.p7 | 18:801805 | GTAATAACTCATCTT[C/T]TGCATGTTTCTTTAT | 7525 |
rs147775423 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | YES1 | GRCh38.p7 | 18:757773 | GTTGCAGTAAGCTGA[C/T]ATCGTGCCAGTGCAC | 7525 |
rs147903919 | in-del | -/G | 0.0520825 | 0.152737 | intron-variant | YES1 | GRCh38.p7 | 18:766483 | CTTTTCTATGTTTTC[-/G]TATTTATGGAAGTAT | 7525 |
rs147961527 | snp | A/G | 0.0107246 | 0.0724382 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724107 | ATTCTGACTTTGGGG[A/G]AAAAAAGAAAGGAAA | 7525 |
rs148015417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:809605 | CGTGCCCAGCCTGAC[A/G]TGTTCAAAGTAGTTA | 7525 |
rs148034301 | snp | A/G | 6.58924e-05 | 0.0057395 | synonymous-codon | YES1 | GRCh38.p7 | 18:747988 | ATTCTTTCCTGTAGC[A/G]ATTGATCTTGCTTCC | 7525 |
rs148037792 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:744597 | GTTTTGCCATGTTGC[C/T]CAGGCTGGTCTCAAA | 7525 |
rs148072218 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | YES1 | GRCh38.p7 | 18:804729 | ACCAGCCTGACCAAC[A/G]TGGAGAAATCCCATT | 7525 |
rs148110254 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:758387 | GAAACACCCCTAACG[C/T]TCACCAAATTTAACC | 7525 |
rs148266489 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | YES1 | GRCh38.p7 | 18:728793 | CCTCCCAAAGTACTG[A/G]GATTACAGGCCTGAG | 7525 |
rs148283132 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:767473 | CAATTTTTTAAAACT[C/T]GATATCTAGTTCTCC | 7525 |
rs148319400 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:725294 | GCAACCTCACCTCAC[A/G]TCCTATCTCCCGCAT | 7525 |
rs148320247 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | YES1 | GRCh38.p7 | 18:796203 | TAGGAATCACAGCCT[C/G]ATGGTTAAGGGTATA | 7525 |
rs148372895 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | YES1 | GRCh38.p7 | 18:791151 | GCTTCTCGGGAGGCT[A/G]AGGCAGGAGAATCGC | 7525 |
rs148415047 | in-del | -/T | 0.134119 | 0.221521 | intron-variant | YES1 | GRCh38.p7 | 18:729458 | ATTTCCATTTGATTC[-/T]TTTTTTTTTTAATAG | 7525 |
rs148422016 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | YES1 | GRCh38.p7 | 18:798116 | TCATGATCATGGTAT[C/G]TCCCCAGCCAGATAA | 7525 |
rs148439667 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | YES1 | GRCh38.p7 | 18:735646 | TTGAATCTGGGAGGC[A/G]GAAGTTGCAGTGAGC | 7525 |
rs148508088 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | YES1 | GRCh38.p7 | 18:751114 | GATGGGAACATGGAT[A/G]GAAGAAAATACGACT | 7525 |
rs148650757 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | YES1 | GRCh38.p7 | 18:773062 | CTCTTTAGCACAATC[C/T]CTTCTTAACATAAGG | 7525 |
rs148664911 | in-del | -/A | 0.00199481 | 0.0315187 | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721149 | TGAATAGCTACACTC[-/A]AAATTACTTAGGTTT | 7525 |
rs148695044 | in-del | -/CAAACAAACAAG | 0.0333695 | 0.124785 | intron-variant | YES1 | GRCh38.p7 | 18:741813 | AAAAAACAAAAACAA[-/CAAACAAACAAG]CAAACAAACAAGCAA | 7525 |
rs148719580 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | YES1 | GRCh38.p7 | 18:788019 | AGCACGTATATGAGA[A/G]AGGCAGGATGCACGC | 7525 |
rs148804968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:769219 | GACACAATGTCAGAA[C/T]ATATTCCTGTCTTTA | 7525 |
rs148810315 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:741142 | ACCTCAAGTGATCTG[C/T]CTGCCTCGGCCTCCC | 7525 |
rs148823914 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:790897 | AGAGCTCCTTCCCAA[C/T]TGTTACCGAGGTTTC | 7525 |
rs148825288 | snp | C/T | 0.00478085 | 0.0486577 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722453 | TCAGGTAAATAATGA[C/T]AGTTAAGAATTATAT | 7525 |
rs148854441 | snp | C/T | 0.000153988 | 0.00877328 | missense | YES1 | GRCh38.p7 | 18:747927 | TGCCATACTCTTCTG[C/T]CTGAATGGAATCTGC | 7525 |
rs148910050 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:743477 | AGGGGCATATAGTGT[A/G]TCAATGTTTTAAGTT | 7525 |
rs148942418 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:799281 | CCCCTTCTATGGTAT[A/G]CAGCCCTCACTGGGA | 7525 |
rs148963347 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | YES1 | GRCh38.p7 | 18:811189 | CCCGTGGAACGTATA[C/T]ACATAATAAATGGAC | 7525 |
rs149030579 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:754204 | AACCTAAACTCGCTA[C/T]CAGAGTCTGTGGGGT | 7525 |
rs149121202 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:778857 | AAAGGGCATACACTT[C/G/T]GTCTTGTAAAAGCAA | 7525 |
rs149131869 | in-del | -/TT | | | intron-variant | YES1 | GRCh38.p7 | 18:778048 | ATGTCTTCAAAGCTC[-/TT]TGTTATTATTATTTA | 7525 |
rs149152590 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:763272 | TCCAGAATTTTTGTT[C/T]TGAGGAATAGCAGAA | 7525 |
rs149171794 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | YES1 | GRCh38.p7 | 18:774216 | CCTTTGCTAACTGTT[C/T]CTCATCTCCCTGACA | 7525 |
rs149275233 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775806 | TGCCTCAAATAAATT[A/T]AAAAAAAAAATAGAA | 7525 |
rs149312331 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:732044 | TTATTAATGGCAGAT[A/G]TATTTATTAAAGTGC | 7525 |
rs149343889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:792778 | TCAGCCTGGGCAACA[C/T]AGAGAGACCTTGTCT | 7525 |
rs149398061 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | YES1 | GRCh38.p7 | 18:785634 | ATGCAACAGTGTTGA[A/G]AGGTGGGATCTTTAA | 7525 |
rs149400716 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:758347 | GGACAAAGTAGATCT[A/G]TACCTTTTCCCTTCC | 7525 |
rs149435542 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | YES1 | GRCh38.p7 | 18:745284 | AATGCATCGTCAGAC[C/G]AAATTTCACTGGATT | 7525 |
rs149489721 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813527 | CAATCATATGTGTCA[A/G]TATTCCGGTATTCTA | 7525 |
rs149492376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:740369 | CCAAATTAAGGCACA[C/T]TTAAAACATAAAAGT | 7525 |
rs149520636 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:801308 | ACTGGAGTCCACCCT[A/G]GGAGACAGAGTGACA | 7525 |
rs149523555 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:767017 | TATGTTTTATGTGTC[C/T]GGAAAATTCTTCACC | 7525 |
rs149540619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:809317 | ATTTGACTTTTTTTT[C/T]TGGAGACAGTCTCAC | 7525 |
rs149612528 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | YES1 | GRCh38.p7 | 18:725050 | TTCTAGTCTTGGTTT[C/T]GCCAAATATACCAAC | 7525 |
rs149634373 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | YES1 | GRCh38.p7 | 18:757099 | CCACAGTATATTGGG[A/G]AAAAACCATGGGCTC | 7525 |
rs149646642 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:780415 | TGGCTTTATAAGAGG[A/C]AGAGAGATCTTAGCT | 7525 |
rs149649622 | in-del | -/AAC | 0.49823 | 0.0296997 | intron-variant | YES1 | GRCh38.p7 | 18:736177 | GACCCTATCTCGAAA[-/AAC]AACAACAACAACAAA | 7525 |
rs149661044 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:730701 | ATGGGCTTCCTTGAT[C/G]CAATGTCCTATCAGT | 7525 |
rs149677138 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:768931 | TGGTCTTGAACTCCT[A/G]ACCTCCAGTGATCCA | 7525 |
rs149799827 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | YES1 | GRCh38.p7 | 18:777738 | CTCTAACCCAGGAGG[C/T]GGAGGTTGCAATGAG | 7525 |
rs149836432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:736493 | TGGCGGTACAGGGCA[A/G]TATCTCCTCTGACTG | 7525 |
rs149925240 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | YES1 | GRCh38.p7 | 18:759603 | TCTGTACTAAATAAC[A/G]TACAGACTTTTTTTC | 7525 |
rs149962387 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | YES1 | GRCh38.p7 | 18:747100 | AGTAATATTCTTTCA[A/T]GGGCATATTACTTTT | 7525 |
rs150045584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:773982 | AATTACATGCGCCCA[C/T]CATCTTGCCCGGCTA | 7525 |
rs150083418 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:757547 | TCTGGGGGGCCAGGC[A/G]CAGTGGCTCACACCT | 7525 |
rs150118620 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722290 | GAGAGTGTCAATACT[A/C]AGCAGGTTACGTAAA | 7525 |
rs150148342 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775672 | CATGGTGGCATACCC[C/G]TGTAGTCCCAGACAC | 7525 |
rs150204854 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:771666 | CTATCCTCCCACCTC[A/G]GCCTCTCTAGTAGCT | 7525 |
rs150235774 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | YES1 | GRCh38.p7 | 18:799107 | CCAATACTGTAACCC[A/G]AATTAAGATACCATC | 7525 |
rs150269292 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | YES1 | GRCh38.p7 | 18:785053 | CCATACTAAGCAACA[C/T]AACTGTTAAATTAGG | 7525 |
rs150361963 | snp | A/G | 1.91653e-05 | 0.00309553 | intron-variant | YES1 | GRCh38.p7 | 18:739828 | TGTAACAGACAGCAA[A/G]ATATTCATAAAAAAT | 7525 |
rs150406339 | in-del | -/CTT | 0.0333695 | 0.124785 | intron-variant | YES1 | GRCh38.p7 | 18:771327 | GCCAAGATTGCACCA[-/CTT]CTACACTACAGCCTG | 7525 |
rs150409550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:808950 | AAGAATAGAAAAACT[A/G]AGGCTGAAATTACTG | 7525 |
rs150415597 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | YES1 | GRCh38.p7 | 18:734904 | GGCTCACGCCTGTAA[A/T]CCCAGCGCTTTGGGA | 7525 |
rs150447619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:761542 | ATTCCTCATCCTCAC[C/T]TCCTTTACCCATAAC | 7525 |
rs150463833 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:803426 | TAAAAAAAGCACAGA[A/G]AAGGTAAAGAAGTTA | 7525 |
rs150497891 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | YES1 | GRCh38.p7 | 18:768912 | TTCCCCATGTTGGCT[A/G]GGCTGGTCTTGAACT | 7525 |
rs150513863 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:809959 | TTTCCCTTCATAGAA[C/G]CACAGGTATTCTATG | 7525 |
rs150532263 | in-del | -/TTTTG | 0.0352966 | 0.128072 | intron-variant | YES1 | GRCh38.p7 | 18:794813 | ATGTGGGTTTTTGGT[-/TTTTG]TTTTGTTTTGTTTTG | 7525 |
rs150554691 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | YES1 | GRCh38.p7 | 18:764377 | ATAGGCATGTGCCAC[C/T]ATGCCCGGCTAATTT | 7525 |
rs150591052 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | YES1 | GRCh38.p7 | 18:725833 | AGGTTGCAGTGAGCC[A/G]AGATTGCGCCATAGC | 7525 |
rs150675462 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:777426 | TTCTAGAAATACTTG[A/T]AGGTTTTCCAACTAT | 7525 |
rs150727563 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:773500 | TCAAAAACTTGAACC[A/G]TGACAGTCATGTTTC | 7525 |
rs150759648 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:801060 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCAAGGAG | 7525 |
rs150764986 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | YES1 | GRCh38.p7 | 18:729658 | TTGAGACAGAGTCTC[A/G]CTCTGTCACCCAGGC | 7525 |
rs150816701 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:796524 | CTGGTAATCTCAGCA[C/T]TTTGGGAGACCGAGG | 7525 |
rs150853039 | snp | A/C/G/T | 0.00199529 | 0.0315338 | intron-variant | YES1 | GRCh38.p7 | 18:755080 | CTATCTTTCCCAAAC[A/C/G/T]TAACTCTAAAAGTAA | 7525 |
rs150887478 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:741397 | ATGTGTGTGCAACCA[C/T]GTCCTGCTAATTTTT | 7525 |
rs150907434 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | YES1 | GRCh38.p7 | 18:749525 | AGCAAAACAAAAAAA[A/C]CCCCTGAATTTCTAG | 7525 |
rs150920374 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | YES1 | GRCh38.p7 | 18:798416 | CTCTTTTCTACTTGA[C/T]ATTTGTTATGAGTTT | 7525 |
rs151115965 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:726922 | GATGAGTAAACAGGC[A/G]CTGTTGCTTTGAAAT | 7525 |
rs151153115 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:745895 | CACTATATCTTTCTC[-/A]AAATACTGCCCCAAG | 7525 |
rs151164477 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:794008 | TACACATTCAGCACA[C/T]GTATCCCAGAACAAC | 7525 |
rs151220504 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:788546 | CCACCCAGAAAGGCA[C/T]TAATATTCTGTGGAA | 7525 |
rs151254312 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:774598 | TCCTCAGTAACCCCC[C/T]GGCCCTATTCTCAAA | 7525 |
rs151256567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:746593 | AAAAGTAAGAAGCAC[C/T]ATAGTAGAACAAAGA | 7525 |
rs151302880 | snp | C/G | 0.000153988 | 0.00877328 | missense, intron-variant | YES1 | GRCh38.p7 | 18:732938 | AGTGCAGCTTCAGGA[C/G]CTGTCCATTTGATTG | 7525 |
rs180686140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:731834 | TAGCTGGGCGTGGTG[A/G]CGGGTGCCTATAGTC | 7525 |
rs180877486 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:811280 | GTATGTTATTCCACG[C/T]CTGTATCAATTAATT | 7525 |
rs180880119 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | YES1 | GRCh38.p7 | 18:763611 | GGGAGGTTGAGGTGG[A/G]AAGATCACCTGAGCC | 7525 |
rs180885391 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:804152 | AACAAGTTGTCCATA[A/C]CTTTGTCAATTAAAA | 7525 |
rs180886012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:782974 | GGCGTGAGCCATCAC[A/G]CTCGGCTAACTTTCT | 7525 |
rs180887743 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:745035 | GCTTGATCAATGTCA[A/G]GATTGCTGGCTGACT | 7525 |
rs180889591 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:793024 | GTCTTAAGGTTCATT[A/G]TAATTATTATTATTA | 7525 |
rs180904553 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | YES1 | GRCh38.p7 | 18:727713 | TTTACCTCTTATTCC[C/T]TGACCCCCTCTACCC | 7525 |
rs180933397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:770969 | ACAGTAGGTACCACC[A/G]CACTCTGCTCTGGGC | 7525 |
rs180951080 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:735477 | AGAGTAATATAATGG[A/C]CTTTGGGGAGTAAGG | 7525 |
rs180973597 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | YES1 | GRCh38.p7 | 18:754725 | TCCAAAAAAAAAAAA[A/C]AAAAATCTCAGCTCA | 7525 |
rs181105211 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | YES1 | GRCh38.p7 | 18:788173 | AATTAATATGGAAAT[A/C]GCATGAATGGTTTTA | 7525 |
rs181108469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:806829 | CTGTACCTCATCCTT[C/T]CTCTGGTTATACAAG | 7525 |
rs181127239 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | YES1 | GRCh38.p7 | 18:766754 | ATCAGTTTTTAAACT[A/G]AAGTGTCTGTTCAAA | 7525 |
rs181218217 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:738676 | GCCTGGGTGACAGAG[C/T]GAGACTCCCATCTCA | 7525 |
rs181219530 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | YES1 | GRCh38.p7 | 18:749017 | AACACAAAAATTAGC[C/T]AGATGCAGCGGCATG | 7525 |
rs181229276 | snp | A/C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722903 | CGAGACTATCCTGGC[A/C/T]AACACGGTGAAACTG | 7525 |
rs181235730 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | YES1 | GRCh38.p7 | 18:732177 | GGCACGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 7525 |
rs181325224 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:804534 | AGAATTGCTTGAACC[C/T]GGGAGGCAGAGGTTG | 7525 |
rs181439385 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:735540 | TGTTGGAGGTGAAAC[A/C]CCGTCTCTACTGAAA | 7525 |
rs181455448 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:794009 | ACACATTCAGCACAC[A/G]TATCCCAGAACAACT | 7525 |
rs181456250 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:755425 | GGCTAATTTTTTTTG[A/T]ATTTTTAGTTGAGAC | 7525 |
rs181574022 | snp | A/G | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812486 | CAGGTCCCCTCCGCG[A/G]GCTCCGGGCCGCTTT | 7525 |
rs181588550 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:771821 | GGTGTGAGCTACCAC[A/T]CCTGGCCTGGAAGAA | 7525 |
rs181630197 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | YES1 | GRCh38.p7 | 18:797674 | TCAAATTGCTTAAAA[A/G]TGATAAACATCTTTT | 7525 |
rs181642363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:758592 | TGCTAAAATCCTATC[C/T]TTTCACTGATGGTCA | 7525 |
rs181650226 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776707 | GATCCTAATCATACC[C/T]GTTTCTACAATTCTG | 7525 |
rs181658567 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:739211 | TAATACTCGTTCTGT[G/T]ACTAACAAGTTTTGT | 7525 |
rs181660148 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723054 | CCGAGATCGCGCCAC[C/T]GCACTCCAGCCTGGG | 7525 |
rs181734350 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:807207 | GGCGTGGTGGTGCAC[A/G]CTTGCAATCCCAGCT | 7525 |
rs181762761 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:767952 | GTGATCCAACCGCCT[C/T]GGCCTCCCAAAGTGA | 7525 |
rs181834401 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:794563 | CTAGGGCTGCTGTAG[A/C]AAAAAAATGGCTTAA | 7525 |
rs181840153 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812930 | ACCATCCTGATCGCC[A/G]TCCAAAAAACGTTCA | 7525 |
rs181854819 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:772307 | GTGCTGGGATTACAG[A/G]CATGAGCCACCGCAC | 7525 |
rs181867048 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:735677 | CGAGATCGTGCCGCT[A/G]CACTCCAGCCTGGGC | 7525 |
rs181867212 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:755700 | CAGCTGTTTTGCCAA[A/G]CCTAAGGATAAAGCA | 7525 |
rs182004191 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | YES1 | GRCh38.p7 | 18:789351 | CTTTGGGAGGCTGAG[A/G]TGGGAGGATGGCTTG | 7525 |
rs182010140 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:782201 | TGCTCATGTGCTTCA[C/T]TCTTCTCTCCTGTGG | 7525 |
rs182012678 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | YES1 | GRCh38.p7 | 18:749649 | TCACAAGGTCAGGAG[A/G]TCGAGACCATCCTGG | 7525 |
rs182034342 | snp | A/G/T | 0.0372196 | 0.131242 | intron-variant | YES1 | GRCh38.p7 | 18:765438 | GAGTCTCGCTCTGTC[A/G/T]CCCAGGCTGGAGTGT | 7525 |
rs182039271 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | YES1 | GRCh38.p7 | 18:787143 | GCTCTGTGGCCCAGG[C/T]TGGAGGAGTGCAGTG | 7525 |
rs182041902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:744825 | CCACATGCCTAACAG[A/G]AGACTGATTTTTTTA | 7525 |
rs182286399 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:803953 | TTATGTTACAGAAAA[A/G]ACTTCCTGGAAAAAC | 7525 |
rs182292307 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | YES1 | GRCh38.p7 | 18:806058 | GCAAAAGTACACCTA[C/T]GAATTATGCATTCCT | 7525 |
rs182299782 | snp | C/T | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813540 | CAGTATTCCGGTATT[C/T]TAGGAACTTAAGGAA | 7525 |
rs182301940 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:764928 | TTTAGTAGAGACCGG[G/T]TTTCACTATGTTGGC | 7525 |
rs182304964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:784863 | AACTCTACCTGCAAC[C/T]GTAACTCCTCTTTAC | 7525 |
rs182308326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:746613 | TAGAACAAAGAGTTA[C/T]TGAGACACATTACAA | 7525 |
rs182313757 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:800796 | CTCATGCCTATAATC[G/T]CAGCACTCTGGGAGG | 7525 |
rs182313865 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:759182 | GCATCAAAATATAAC[C/T]GGGGCTAGGCGCGGT | 7525 |
rs182323293 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:762866 | TGTATGAAACAAATA[C/T]AACACTGTACAATGT | 7525 |
rs182327020 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:729380 | AGATCGTGCCACTGT[A/G]CTCCAGCCTGGGAGA | 7525 |
rs182329411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:727057 | AAAGTATCTCTTTTT[C/T]TTCTTTAAAGATGGG | 7525 |
rs182334214 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723716 | GTTACCTTCATTATT[C/G]TAAGTCAAACTCTTC | 7525 |
rs182448683 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:741644 | TCCCATCTGTAGAAA[A/C]ATACACAAATTATCT | 7525 |
rs182451961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:759798 | ATGTGCCATGTTGGT[A/G]TGCTGCACCCATTAA | 7525 |
rs182461555 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:724698 | GGAAAACATAACAAA[A/C]CCCCTAGCCACTAAC | 7525 |
rs182542061 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:808516 | GTTGTGCCTCGCTAT[A/G]GGACTTATATTATAA | 7525 |
rs182554065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:791599 | CACAAATACAAACCA[C/T]ATATGCAATTTTAAA | 7525 |
rs182566804 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:777170 | GCTGGTGAAGTACAA[A/C]ATAGAAGAACAAGAA | 7525 |
rs182588906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:806740 | TGGGAGCACAAAGAG[A/G]TCATAACACCAATCT | 7525 |
rs182594090 | snp | C/T | 0.000209518 | 0.010233 | intron-variant | YES1 | GRCh38.p7 | 18:739825 | TCCTGTAACAGACAG[C/T]AAGATATTCATAAAA | 7525 |
rs182608896 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:772750 | ATCTCTATTTCTGTA[C/T]TTCTGATGTTTCTGG | 7525 |
rs182611238 | snp | A/G | 0.00189744 | 0.0307437 | intron-variant | YES1 | GRCh38.p7 | 18:736989 | AAAACAAAAAACACA[A/G]GACATACGATACAAA | 7525 |
rs182669529 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:783506 | CTCAATTGAGTTGAA[C/T]TGGAAAAACCAGGAG | 7525 |
rs182677050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:757241 | GGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 7525 |
rs182677249 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:763883 | TCCCAGCACTTTGGG[A/G]GGCCGAGGCGGGCAG | 7525 |
rs182683006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:737732 | TTACATTTTGATTGA[C/T]TGACTGAGACGGGGT | 7525 |
rs182684758 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:721611 | ATAATGTTCTGAATT[G/T]AATAAAGGATTGATT | 7525 |
rs182850069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:751197 | TTGCTAATGAAATTA[C/T]TCGATCTACTTTCTA | 7525 |
rs182868365 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:778163 | AGAGAGGTTATTACA[C/T]GCCTTGCTCAAGGAC | 7525 |
rs182871460 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:795308 | ATTAACTTTCAAATG[G/T]TGGTGGTGGGGACAC | 7525 |
rs182892368 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:801701 | TATATATGTATAGAG[A/T]GTGTGTATGTGTATA | 7525 |
rs182899380 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:760804 | TCCACATTGAGAGGG[A/G]CAGGGGTGGGGACAG | 7525 |
rs182902941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:778470 | AAAAATTTTCAAATG[A/G]TTTAACACATTTCTG | 7525 |
rs182915110 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | YES1 | GRCh38.p7 | 18:742700 | AAACTTAATTTCAAA[A/G]TTAATTCAGCCTGCC | 7525 |
rs183105894 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:796491 | AACAAACAATTAGGC[C/T]GGGTGCAGTGGCTCA | 7525 |
rs183130352 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:774457 | ATTTCCAAGAAACCT[A/C]ATCTTCCTCCCCAAA | 7525 |
rs183130628 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:795977 | GTAAAACAAAAGTTC[A/C]GAGTCTATATAATAA | 7525 |
rs183149261 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:801146 | GCGAGACTCCATCTC[A/C]AAAAAATATAAAAAT | 7525 |
rs183158449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:769249 | AAAGTGACGTGCGAC[C/T]GTAAGTAAATCTGTA | 7525 |
rs183168297 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:734096 | CCAGCCTGGCCAACA[C/T]GGTGAAACCCTGTCT | 7525 |
rs183219723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:728754 | TGGTCTCAAACCCCT[A/G]ACCTCGTGATCCACT | 7525 |
rs183404831 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:773236 | AATGTTTAATGCTGA[G/T]CCAGCTCTACTAAGT | 7525 |
rs183449247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:746118 | TATACAGAAGTGTCA[A/G]TAAGAATGGACTGGG | 7525 |
rs183485494 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:732657 | TTCACTGACTTACCC[A/G]TCCAATGCCACAGTT | 7525 |
rs183523407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:790151 | GAGACCAAGGTGGGC[A/G]GATCACCTGAGGTCA | 7525 |
rs183529486 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:808317 | CTGCCTCTGAGTTTA[C/G]ACAGGAGCTGGATGG | 7525 |
rs183530878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:768861 | GCATCTGCCACCACG[C/T]CTGGCTAATTTTTGT | 7525 |
rs183548201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:750503 | TCACTAGAAGACAGC[A/G]GCAGCACCCCAACTG | 7525 |
rs183552542 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:733080 | AGTCATCAGTGTCAA[C/T]TCTTTAAATGTACAA | 7525 |
rs183586541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:787667 | GTGAGCTGAAATCGC[A/G]CCACTGCACTTCAGC | 7525 |
rs183589696 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:806798 | GTACTTCTTACTGTT[A/C]AAATGCATGGTCTAA | 7525 |
rs183593079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:765714 | ATTTAACACTTTTTA[A/G]TAAGGAGTAAAATAA | 7525 |
rs183611645 | snp | A/G/T | 0.000560093 | 0.0167259 | intron-variant | YES1 | GRCh38.p7 | 18:748045 | AAAACAGCAATCACC[A/G/T]CAAGGTAGACTATTG | 7525 |
rs183717766 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:725524 | AAAACTCTACATGAC[A/G]TTACTTTGAAACTCA | 7525 |
rs183719968 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:784518 | TAAAACAATACAAAC[A/G]TATTTATCTTACAGT | 7525 |
rs183744689 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:746424 | GTAACAGCATCATCA[C/T]CTGCATTCAGTAAGA | 7525 |
rs183914588 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:804989 | AGAACTGCAATTTGC[C/T]TGAGAAAGTTCCGTG | 7525 |
rs183945505 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:764421 | GAGACAGAGTATCAC[C/T]ATGTTTGTCAGGCTG | 7525 |
rs183971282 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:728968 | GTTCACTTAATCTGT[A/G]GGCTAGTATTTTGTT | 7525 |
rs184028814 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:779972 | GGTGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 7525 |
rs184038082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:802287 | TAATTAGAAAGTATT[A/G]CCAGGCGTGGTGGCT | 7525 |
rs184039626 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:762380 | TGGAAACCTACCTGT[G/T]GGATATTACACTGAT | 7525 |
rs184040093 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:744221 | AAATGGTAGAGATGG[A/G]ATTCAAATCTAGGTC | 7525 |
rs184041998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:726695 | CTGAGGCAGGAGAAT[C/T]ACTTGAACCTGGGAG | 7525 |
rs184047706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:761916 | TCATGGCTGGGCATC[A/G]TGGCTCATGCCTGTA | 7525 |
rs184060757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:725809 | GAGAATCACTTGAAC[A/G]GGAGGCGGAGGTTGC | 7525 |
rs184173500 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:779383 | CACTCCAGCCTCGGA[A/G]ACAGAGTGAGACCCT | 7525 |
rs184202276 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:743494 | CAATGTTTTAAGTTT[A/C]AACTGTAGAAAAACA | 7525 |
rs184269710 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776507 | GTTCAAGACACTTAT[A/C]CATTGTTCTATAGGG | 7525 |
rs184280288 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:785891 | TGCAGTGAGCCAGGA[C/T]TGTGCCACTGCACTC | 7525 |
rs184281556 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:738734 | ATACACTTTAGATTA[C/T]TAATATTTTCTTTGG | 7525 |
rs184282897 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | YES1 | GRCh38.p7 | 18:757418 | TGAGGCAGGAGAATG[A/G]CGTGAACCCGGGAGG | 7525 |
rs184283325 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:806283 | AAACCTTACTAGAGA[C/G]TAGTTTAACTTCAAC | 7525 |
rs184292401 | snp | C/T | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722906 | GACTATCCTGGCTAA[C/T]ACGGTGAAACTGCGT | 7525 |
rs184327254 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775573 | AAGCCAAAGCAGGAG[A/G]ATTGTGTGAGCCCAG | 7525 |
rs184351527 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | YES1 | GRCh38.p7 | 18:738506 | CCATCCTGGCGAACA[C/T]GGTGAAACCCCGTCC | 7525 |
rs184458934 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:796856 | CACTAAAAGGTGGCA[C/T]TTTGAACCAGTGTGA | 7525 |
rs184463769 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | YES1 | GRCh38.p7 | 18:757311 | GATTGAGACCATCCT[A/G]GCTAACACGGTGAAA | 7525 |
rs184494406 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722780 | AAGGGAAAAAATGAC[C/T]ACCATTACATAGACT | 7525 |
rs184501243 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:781295 | AAAAAAATAAGAGGG[C/G]CTTGTATGATTTGCT | 7525 |
rs184509760 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:803723 | TGGTAAGGTGGGAAA[A/G]GAGGGTGACTGGCAA | 7525 |
rs184512260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:762709 | AGAATTCACCACTAC[A/G]TAATTCATCCATTTA | 7525 |
rs184576646 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:731097 | AAATTGCTAGGGTTG[A/G]GGTGGAGGGAGTTAT | 7525 |
rs184580137 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | YES1 | GRCh38.p7 | 18:757289 | CGGGCGGATCACGAG[G/T]TCAGGAGATTGAGAC | 7525 |
rs184581649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:793048 | ATTATTATTGGTTTT[C/T]TTTTTTTTTTGAGAC | 7525 |
rs184589031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:755194 | ATTGACTTAACATGC[A/G]TAACTCCCTAAATGA | 7525 |
rs184596570 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:737921 | GATGGGGTTTCACTA[A/T]GTTGCCCAGGCCCCG | 7525 |
rs184699143 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:811339 | ACTGTTAAGTCCTAC[G/T]CATTACAAAACAAAA | 7525 |
rs184723473 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:802874 | GATCGCTTGAGCCCA[A/G]GAGTTCGAGACAGCC | 7525 |
rs184727295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:771196 | ACATGGCGAAACCTC[A/G]TCTCTACTAAAAATA | 7525 |
rs184730459 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:735483 | ATATAATGGACTTTG[C/G]GGAGTAAGGGGGAAA | 7525 |
rs184790444 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:792811 | ATTTTTTAAAAAAAT[G/T]TAAAAAAGAAAGAAA | 7525 |
rs184800857 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:811002 | CTTAAATGCACAGTC[A/G]CGTGTATACATTTAG | 7525 |
rs184809768 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:770731 | GATCACAGTCCTGCA[C/G]TGCTGTTGTCCAAAG | 7525 |
rs184816605 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:735011 | AAAATACAAAAATTA[C/G]CCGGGCCTGGTGGCA | 7525 |
rs184864821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:797085 | GGAACATTATGCACA[A/G]ACATGGAAAAGTCTT | 7525 |
rs184911464 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:765054 | GAATCTTTTAAAGAT[A/C]ACAGAACTCTCAAAT | 7525 |
rs184921838 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:730405 | GCTGGAGTGCAGTGG[C/T]GCAATCATAGCTCAC | 7525 |
rs185029078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:747200 | TTGGGCCAGGCACAA[C/T]GGCTCACGCCTGTGA | 7525 |
rs185071703 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:731896 | GGCGTGAAGCTGGGA[A/G]GTGGAGGCTGCAGTG | 7525 |
rs185151394 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | YES1 | GRCh38.p7 | 18:809104 | TTTGATGACAGAACA[C/G]TATCCATTCGTTCAA | 7525 |
rs185160270 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:744625 | AAACTCCTGACCTCA[A/C]GTGATCTGTCTGTTT | 7525 |
rs185163235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:769688 | ATATAGGTTTTTTTC[C/T]TTTATTCAATTGATG | 7525 |
rs185276363 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:804227 | AATGTTGCAAAGTTT[G/T]TATTCAAATAGCCAC | 7525 |
rs185284191 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:792608 | ATATATACATATATA[C/T]ACATACATATATATA | 7525 |
rs185284488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:763659 | CAGTGAGCTGTGATC[A/G]TGCCACTGCACTCCA | 7525 |
rs185286413 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:753270 | GTAGAGCTAATTAAC[A/G]TATGCATTGCATCAC | 7525 |
rs185288530 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:783192 | AATTTGAGTCTGCCT[A/G]GGCAAAATAGCTAGA | 7525 |
rs185290377 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:726995 | GCTACATGTGGAAAG[G/T]TCTTTCCAAATCCTC | 7525 |
rs185293600 | snp | A/C/T | 0.000380448 | 0.0137871 | missense | YES1 | GRCh38.p7 | 18:745836 | ATCTCATCCCAATCA[A/C/T]GAATAGAAAGGGAAT | 7525 |
rs185308116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:727893 | CTGTCTGACTGTTGT[C/T]CCTGCGTAGATAATA | 7525 |
rs185409734 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:786119 | ACCAAATCTGTGGTA[C/G]TGTTATAGCAACACA | 7525 |
rs185414861 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:747658 | TATGCAAAAGGCTTA[C/T]AGATACATATTTAAG | 7525 |
rs185447950 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722492 | TAGAGGGGCCTAATA[C/T]AAGGCTTAATTTAAA | 7525 |
rs185519250 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:806649 | ACACAGTGAATACTA[A/G]GTCAAGAATAACAGA | 7525 |
rs185528308 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:801169 | ATAAAAATAAAAAAT[A/T]AAAATAAAATAAAAT | 7525 |
rs185536230 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:806937 | AGATAAGTCAAAGGA[A/G]TATCTCCAGATTTTC | 7525 |
rs185544978 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:778286 | GTGTATAGCATTCTT[C/T]GTTCATTGGTAAGTT | 7525 |
rs185546006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:765187 | TTGGGAATACCTCCA[C/T]AGATACGAAAAGATA | 7525 |
rs185554770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:759816 | CTGCACCCATTAACT[C/T]GTCATTTACATTAGG | 7525 |
rs185555180 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:742331 | TTCCATTGAAGGTAG[C/T]GGGGAGGCCAGGCAC | 7525 |
rs185803922 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:804558 | GAGGTTGCAGTGAGC[C/T]GAGATTGCACCACTG | 7525 |
rs185892698 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:777293 | ATATAAAGACATTCA[C/T]TTAATTTTGTTGGAA | 7525 |
rs185922824 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:739905 | ATCACAACACAAAAC[G/T]TCTTAGCTTTTCATT | 7525 |
rs186046090 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:759549 | AGTTCTGCATCCATG[A/G]ATTCAGCCAAGATTC | 7525 |
rs186053629 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723993 | AAACTGGAATGGAAT[C/T]ATTTGGTCCCATGAT | 7525 |
rs186067724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:755450 | TGAGACAGTGTTTTG[C/T]CATGTTGCCCAGGCT | 7525 |
rs186075982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:735588 | GTGTGGTGGTACGAG[C/T]CTGTAATCCCAGCTA | 7525 |
rs186152382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:795508 | TGGAACCAACCCATA[C/T]CCCCATCAATGATAG | 7525 |
rs186267069 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813745 | CTTTTATTAAAATAG[A/G]AAATTCCTTGAGCTG | 7525 |
rs186291521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:750453 | GAGGCTGCTGTGTGC[A/G]TTTTAAGATATTTAC | 7525 |
rs186294648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:798341 | TTTTCCTTTTCTGAA[A/G]CATCGGTCATTGTAA | 7525 |
rs186297285 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:732751 | AGAAATAAAGGCCTT[C/T]TCCCCGCTTACAATT | 7525 |
rs186298779 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:758880 | AATCTGCATTATTCT[A/T]TTCACTGTCTACAGA | 7525 |
rs186300210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776907 | TAACCAGGCATTCCA[A/G]GTTAACTTCCCCAAC | 7525 |
rs186470024 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:767196 | GTCTGGCTACTCTGG[A/C]TGGAGTACAGTGACA | 7525 |
rs186476608 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813053 | CGAAGCTGAGTTCTG[C/T]TTGGCGACTATCCCA | 7525 |
rs186477970 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:732299 | CAAAAAATTAGCTGG[C/G]TGTGGTGGTGGGTGC | 7525 |
rs186490543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:794962 | CTCGAACTACAGGCG[C/T]GTGCCACCATGCCTG | 7525 |
rs186506119 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:772698 | CGGCCTCTCAAAGTG[C/G]TGGGATTACAAGTAT | 7525 |
rs186510986 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:756113 | TTTTAAATCAGCAGC[A/G]TCTGGGAGAAATTCT | 7525 |
rs186513676 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | YES1 | GRCh38.p7 | 18:735979 | AGTTCGAGACCAGCT[G/T]GGGCAACATGGCAAA | 7525 |
rs186645870 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:788435 | ATTGTTTAAAATATG[C/T]ACATAATAACGATGT | 7525 |
rs186657024 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:749518 | AAACAAAAGCAAAAC[A/C]AAAAAACCCCCTGAA | 7525 |
rs186680851 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:783834 | GGCCAGGCTAGTCTT[G/T]AACGCCTGACATCAG | 7525 |
rs186695548 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812513 | CTTTGCTGTGGTCAG[C/G]ATAGGCGACCGGTCC | 7525 |
rs186699321 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:772010 | TACAAGACAGTCTGA[A/T]CGTACACCACAAAAG | 7525 |
rs186704949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:791119 | GCCGGGCGTGGTGGT[A/G]CGCGTTTGTAATCCC | 7525 |
rs186711764 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:746132 | AGTAAGAATGGACTG[C/G]GATAGGTTTGGACGA | 7525 |
rs186721586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:808324 | TGAGTTTAGACAGGA[A/G]CTGGATGGTTAGTAA | 7525 |
rs186723567 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:769101 | GAGCCATAGGCTATA[C/T]CATATAGCCTAGGTA | 7525 |
rs186731271 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:725815 | CACTTGAACGGGAGG[C/T]GGAGGTTGCAGTGAG | 7525 |
rs186739093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:733210 | TGTGGGAACAGAAAA[C/T]AATTTAAGAAAATAG | 7525 |
rs186742300 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:751047 | GTACTGAATATTTTA[A/C]AAGTAGAAGGATATG | 7525 |
rs186914740 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | YES1 | GRCh38.p7 | 18:763896 | GGAGGCCGAGGCGGG[C/T]AGATCATGAGGTCAG | 7525 |
rs186924856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:728791 | GACCTCCCAAAGTAC[C/T]GGGATTACAGGCCTG | 7525 |
rs186926731 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:794201 | ATAGACTAACACAGC[A/G]TGCCTCCTGATGTCT | 7525 |
rs186953730 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:806130 | TTTGTCCTAGGTATA[C/T]ATGAACAAGTCATAA | 7525 |
rs186959900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:765003 | CCTCCCAAAGGGCTG[A/G]GATTACAGGCGTGAG | 7525 |
rs186968064 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:784926 | ATTCACAGAACATGG[A/C]CATCTCTGGGGAGTC | 7525 |
rs186981442 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:746727 | GTAGCGTTTATGAAT[C/T]CCAGATAAACTGGTT | 7525 |
rs186987790 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:729839 | ACCATCTTGGCCAGG[A/C]TGGTCTCAAACTCCT | 7525 |
rs186992016 | snp | C/G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:789816 | TGTAATCCCAGCACT[C/G/T]TGGGAGGCTGAGGCA | 7525 |
rs187007055 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:779239 | AGACCCCCGTCCCGG[A/C]AAAAAATTTTTTAAA | 7525 |
rs187036941 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723201 | AATGAATGTGAAGCC[A/G]TAACTTCATTATTTT | 7525 |
rs187092938 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | YES1 | GRCh38.p7 | 18:725215 | AGCAGTTCACCCCAT[A/C]TTATCACAGGACAGC | 7525 |
rs187164491 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:807925 | TGAAGTATAATGCTT[C/T]AAGGAACCTGCAGTC | 7525 |
rs187193750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:768287 | TACAAATTTTAATCA[C/T]ACAAATTTTAGAATC | 7525 |
rs187231684 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | YES1 | GRCh38.p7 | 18:739487 | CTGTGCCTGCAGTCC[C/T]AGCTACCCAGGAGGC | 7525 |
rs187286701 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:796217 | TCATGGTTAAGGGTA[C/T]AGGCTCTGGAGTCAC | 7525 |
rs187294776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:804084 | CCATTTTCCAATGCC[A/G]TGCTTGTCTTGTTCT | 7525 |
rs187296030 | snp | A/C/G | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:773926 | AACCTCCACCTCCTG[A/C/G]GTTTGAGCAATTCTC | 7525 |
rs187310056 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | YES1 | GRCh38.p7 | 18:737863 | TAGCTGGGACTTAGG[C/T]ATGCGACACCACACC | 7525 |
rs187311991 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | YES1 | GRCh38.p7 | 18:757259 | CTGTAATCCCAGCAC[G/T]TTGGGAGGCCAAGGC | 7525 |
rs187321798 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:763240 | ACTTTTAGACTTTCT[C/T]CAGGGAGCATTAGGA | 7525 |
rs187329722 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:727276 | TTAAAGTCTACTGCT[A/G]TCTAGGCTTTCTTCA | 7525 |
rs187513126 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:769765 | ACCTTTGCATTCTTG[A/G]GATAAAACCCAATTG | 7525 |
rs187521706 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:779413 | TGTCTCAAAAAAAAA[A/G]AAAAAAGAAAGAAAG | 7525 |
rs187523021 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:778595 | AATAGCCCTAGTCTG[C/G]CATTTTGCCCAGATG | 7525 |
rs187525910 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:801855 | TAGGAAAAAAAGAAA[C/G]TTGATTGGGAAAACA | 7525 |
rs187530267 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:753423 | ATCCTTTAGCCAACA[A/T]ATTTTTAATTTGAAT | 7525 |
rs187532222 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | YES1 | GRCh38.p7 | 18:734513 | GTGAGCCAAGATCGC[A/G]CCACTGCACTCCAGC | 7525 |
rs187534230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:743561 | CAAAACAAAAAGGGA[A/G]TTGTCCATAAGCAGC | 7525 |
rs187566684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:782362 | CAGCTTGGATCAGCC[A/G]CCTCCCTCTGGGTCA | 7525 |
rs187579244 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:744894 | AACAGCTTGACTTAT[G/T]AATTCTGCTTATACA | 7525 |
rs187760688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:802646 | TCTCCCTTTCCATCA[C/T]TGCTCCTCATTCCTA | 7525 |
rs187786537 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:757193 | TATGTTGCTTAACCT[C/T]TATGCACTCCAGTTA | 7525 |
rs187789566 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:796645 | GGTGGCAGGCATCTG[A/T]AGTCTCAGTTGCTGA | 7525 |
rs187790223 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:761976 | AGGATCACCTGAGGT[C/T]GGGAGTTTGAGACCA | 7525 |
rs187796473 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | YES1 | GRCh38.p7 | 18:757307 | AGGAGATTGAGACCA[C/T]CCTGGCTAACACGGT | 7525 |
rs187800959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:774899 | CTTCAACTCCTACTA[C/T]TGTGCCCCAACTTGC | 7525 |
rs187968637 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:729253 | TGTTTTACAGTTCTA[A/G]AATTTCCATTTGAGG | 7525 |
rs188010219 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | YES1 | GRCh38.p7 | 18:808929 | CTGAGATTTCATGGC[A/G]TTCTTAAGAATAGAA | 7525 |
rs188015605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:811065 | GAAGTGTAACAGGAT[A/G]GTTTAAATATTTAAA | 7525 |
rs188031497 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:745006 | TTACAAGTGATGCCA[C/T]TGCTTGGTAACATGC | 7525 |
rs188033345 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | YES1 | GRCh38.p7 | 18:792869 | AAGCCAAGGGGGGGG[A/G]AAAAGCTTAAATCAA | 7525 |
rs188036818 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:769312 | ACTGTACTAAACTCT[C/T]ATGATTTCTAGTACT | 7525 |
rs188053123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:727423 | TCTTATCTTTTTTTA[C/T]TGGAATGTTTAGTGT | 7525 |
rs188053264 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:770814 | TTTGTGGAGGTGTGG[A/G]GGTTGACAGATGGTA | 7525 |
rs188053887 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:734119 | CCCTGTCTGTACCAA[A/C]AATACAAAACTTAGC | 7525 |
rs188056499 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:772870 | GGTTCCCTCTATCTT[C/G]CACAGCACTTTAATT | 7525 |
rs188061199 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | YES1 | GRCh38.p7 | 18:754564 | ACAAAAAAAATTAGC[C/T]GGGTGCCGTGGTGTT | 7525 |
rs188078358 | snp | C/G | 0.00137957 | 0.0262275 | intron-variant | YES1 | GRCh38.p7 | 18:737005 | GACATACGATACAAA[C/G]GGAAGCAGAGAGAAG | 7525 |
rs188265819 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | YES1 | GRCh38.p7 | 18:785971 | CTCCCTCACTCTAAC[A/C]CTCTCTCAGCCTCTT | 7525 |
rs188276575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:787762 | TTCCCCATCATCATT[C/T]AGGACCTGACCCAAA | 7525 |
rs188287520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:806820 | ATGGTCTAACTGTAC[C/T]TCATCCTTCCTCTGG | 7525 |
rs188291174 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:766133 | GTTGATCCTTCTTAC[C/G]TTTGCCAAGTCCTTC | 7525 |
rs188309179 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:792498 | GTGAATAGCACTATA[C/G]TCCAGCCTCAGAAAC | 7525 |
rs188310345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:748661 | GGTCTTTTGTAATTG[A/G]CTTCTTTTACTTGGC | 7525 |
rs188317494 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:752328 | TTAGCCAGGTTGGTT[C/T]TGAACTCCTGGCCCC | 7525 |
rs188540586 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | YES1 | GRCh38.p7 | 18:806561 | AACCACATCCCTACA[A/T]ACAATTCAGAATTTA | 7525 |
rs188548275 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:792756 | GCTTGAGGCCAGGAG[C/T]TCAAGATCAGCCTGG | 7525 |
rs188565911 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:761115 | TTTTGACTCAATATA[A/C]TTAAGCCTGAAGGCA | 7525 |
rs188572645 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | YES1 | GRCh38.p7 | 18:765080 | CAAATAATGTACAGC[C/T]TTAGAGGAAATCAAA | 7525 |
rs188593937 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:725567 | AAGTTTTCTGAGCTT[G/T]TCATCTAACTAGGTA | 7525 |
rs188706979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:762631 | ACATACATTATGGGA[C/T]TAAAAAAAACTATAT | 7525 |
rs188708702 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:780700 | GCCCTGTAATCTCTA[A/G]AATTCTTCCATTTCT | 7525 |
rs188725167 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:744223 | ATGGTAGAGATGGGA[C/T]TCAAATCTAGGTCTG | 7525 |
rs188727492 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:726919 | TAAGATGAGTAAACA[A/G]GCGCTGTTGCTTTGA | 7525 |
rs188817367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:805020 | TCAAGTCCATGGGTC[A/G]GTTTTTTATAATCTT | 7525 |
rs188817611 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:809258 | TAGAACTTTATTTAG[A/G]AATTTTTTCCCAAAA | 7525 |
rs188836292 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:738143 | CATATGCCTGTTGCC[C/T]ATGTATAGTTTCTCA | 7525 |
rs188847545 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:764755 | CTCTTTTTTTTGAGA[C/T]GGAGTCTCGTTCTGT | 7525 |
rs188857712 | snp | C/T | 3.30022e-05 | 0.00406202 | missense | YES1 | GRCh38.p7 | 18:743272 | TACCCATCCACACTT[C/T]GCCGAAACATCCTTG | 7525 |
rs188942260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:797241 | GAGAGATGCATAGTA[A/G]CCTTCAATTGAAAAA | 7525 |
rs188958746 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776594 | AGGAGTAGGATTTAG[C/T]GCATTTACTCCTGTA | 7525 |
rs188966962 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:757756 | GAACCCAGGAGGAAG[A/T]GGTTGCAGTAAGCTG | 7525 |
rs188969566 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | YES1 | GRCh38.p7 | 18:739021 | GTAGAGACAGAGTTT[C/T]ACCATGTTGGCCAGG | 7525 |
rs188975592 | snp | A/G | 0.02016 | 0.0983543 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722965 | GGCGTGGTGGTGGGC[A/G]CCTGTAGTCCCAGCT | 7525 |
rs189046472 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:782749 | ACCCAGGTTGGAGTG[C/G]AGCGGCACAATCTCG | 7525 |
rs189114248 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:784549 | TCAGAAGTCTGACGC[C/T]GGTGTCCCTGGACTA | 7525 |
rs189118101 | snp | A/G | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722711 | CCCCTTTTCACCACC[A/G]TTAATATTCAGAATA | 7525 |
rs189120187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:746464 | ATCATACCCAAATTA[C/T]TAGTAACTCTAAATA | 7525 |
rs189215905 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:803816 | AGAGCTCAGCAGTTA[A/C]CAAAAACCAGGCAAA | 7525 |
rs189311929 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:804132 | GTATAAAGACAAATA[C/T]CCAGAACAAGTTGTC | 7525 |
rs189332545 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:796925 | CTGAGGAAAAAAAAA[A/T]TACCTCACAACATAC | 7525 |
rs189339977 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:765363 | GTGTTAAATGTGGAT[A/G]AATTATTTTTGTTTG | 7525 |
rs189341648 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:763245 | TAGACTTTCTCCAGG[A/G]AGCATTAGGAATCCA | 7525 |
rs189347625 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:757364 | AAAAATTAGCCGGGC[A/G]TGGTGGTGGGCGCCT | 7525 |
rs189350265 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:747787 | ATTTTTAAGTAACAT[C/G]TATTAATATGATACA | 7525 |
rs189358268 | snp | A/C/G/T | 0.00557734 | 0.0525397 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722888 | ACAAGGTCAGGAGAT[A/C/G/T]GAGACTATCCTGGCT | 7525 |
rs189363898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:731559 | TTATATGCTTTCACT[C/T]TCAACATTAGGATAC | 7525 |
rs189365072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:735015 | TACAAAAATTAGCCG[A/G]GCCTGGTGGCAGGTG | 7525 |
rs189462564 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:799178 | ACCAAGTGGTATTTT[C/G]CATACAGATGTCTAA | 7525 |
rs189565253 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:811780 | GGGCAAAAATAAACC[G/T]CTCCTCCCCGTCGCC | 7525 |
rs189575591 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:771384 | AAAAAAAAAAAAATT[C/T]ATTTGAGTGCAGAGG | 7525 |
rs189598676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:735523 | GTGGATAAAAGACTA[C/T]ATGTTGGAGGTGAAA | 7525 |
rs189611397 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775916 | GCTGTACTTTGTTTT[C/G]ACTTCTGTGTAGCAT | 7525 |
rs189636712 | snp | A/G | 0.029116 | 0.117091 | intron-variant | YES1 | GRCh38.p7 | 18:738636 | TGGAGCTTGCAGTGA[A/G]CCGAGATTGCACCAC | 7525 |
rs189678205 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813534 | ATGTGTCAGTATTCC[A/G]GTATTCTAGGAACTT | 7525 |
rs189696184 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:795150 | GAACATAACTGAATC[C/T]GCAACTGCAAATTAG | 7525 |
rs189709240 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:772734 | ACCACGCCCGGCCAG[C/T]ATCTCTATTTCTGTA | 7525 |
rs189851847 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:793319 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCT | 7525 |
rs189855220 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:740386 | TAAAACATAAAAGTG[A/G]TCTATTCTCTTCAGA | 7525 |
rs189857797 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:755280 | TGGAGACAGAGTCTC[A/G]CTCTGTCACCTAGGC | 7525 |
rs189907712 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | YES1 | GRCh38.p7 | 18:747294 | GGCCAATAGGCGAAA[C/T]CCCGTCTCTACTAAA | 7525 |
rs189923147 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:808456 | GAACTACCAATAAGA[A/C]AAGACACTTTAATAG | 7525 |
rs189940077 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:791518 | AGGTAACTAGTCTAA[C/G]GTCAAAGACACTCTC | 7525 |
rs190087747 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:804320 | ATTTTATTACGAAAA[A/C]ATCTGGGCTAGGCAC | 7525 |
rs190095670 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | YES1 | GRCh38.p7 | 18:763742 | ACGAGCTGGAACAGT[C/G]TGGGGCCAGTGATAA | 7525 |
rs190100985 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:783469 | TATGAATGCAATGTT[A/G]TAACAAAATTGAATC | 7525 |
rs190102686 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721313 | GAGGCCGAAGCGGAC[A/G]GATCACGAGGTCAGG | 7525 |
rs190121703 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:727993 | TTTTGGAATATTTGC[A/G]TATACATAATGAGAT | 7525 |
rs190139464 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | YES1 | GRCh38.p7 | 18:762714 | TCACCACTACATAAT[G/T]CATCCATTTAACCGA | 7525 |
rs190156750 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:727049 | TGAATGATAAAGTAT[A/C]TCTTTTTCTTCTTTA | 7525 |
rs190163856 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:730466 | CCACCCACCTTAGCC[C/T]CCCAAAGTGCTGGGA | 7525 |
rs190331836 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:801225 | GTGGTCGCAGCTACT[G/T]GGGAGGCTGAGGTGA | 7525 |
rs190345968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:760022 | GCTTCATCCATGTCC[C/T]TACAAAGGACGTGAA | 7525 |
rs190346269 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:778455 | TTAGTAACAGTGACT[A/G]AAAATTTTCAAATGA | 7525 |
rs190360338 | snp | C/T | 0.0126979 | 0.078662 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812621 | AGGAGGAGGTGCTTC[C/T]CTGCCCGGAGAGCAG | 7525 |
rs190361999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:742657 | CTTTCTATTTTTCAC[C/T]TTTCTAGCTTTTCCA | 7525 |
rs190364131 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:725333 | TTCCCTGCCTGCAAG[C/T]CAGGCCATCCCTTGT | 7525 |
rs190380725 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:781784 | TTTTTTGGAGGAATA[A/C]TACCTATCTTGCAAG | 7525 |
rs190388843 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:806674 | AACAGACAAGCATGG[A/C]AAGAAATAATTACAG | 7525 |
rs190393067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:777084 | TATTTCTGAAGCAGA[A/G]GCAGCAGGATGTGCA | 7525 |
rs190403819 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:744732 | AGAGATGAGGTCTTG[C/T]TATGTTGCCCAGGCT | 7525 |
rs190621626 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:784772 | TCCACTCTTAAAAAC[A/C]ATTGTTACTCTATTA | 7525 |
rs190638894 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:759136 | TCACTCTCTTAAATT[C/G]GTATATTCTAAAGAT | 7525 |
rs190639547 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:756213 | AAAGTACTTTACAAT[A/C]CTGAGAAGTTGTCAA | 7525 |
rs190660972 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:786343 | CCTCCCTAGAGTAGG[A/G]GGAAGGGGAGCTTCA | 7525 |
rs190750241 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:794508 | AAATATATGAACTAC[A/T]GTATTACTTTCCTTG | 7525 |
rs190762694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:772012 | CAAGACAGTCTGATC[A/G]TACACCACAAAAGCA | 7525 |
rs190779010 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:735673 | GAGCCGAGATCGTGC[C/T]GCTACACTCCAGCCT | 7525 |
rs190851061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:805799 | AGGAAACAATGTGAA[A/G]TATTAACTTATACAC | 7525 |
rs190881206 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:800997 | CTAAAAATATAAAAA[A/T]TAGCTGGGTGTGGTG | 7525 |
rs190898963 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:733376 | TCCTACTTTTTATAT[A/C]ATTCTGGAAAATTTT | 7525 |
rs190909355 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:736533 | GGCCTTTCTAGGAAA[G/T]AAATTAAAATATATT | 7525 |
rs190914191 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:759765 | CATGTGCACAACGTG[C/T]AGGTTACATATGTAT | 7525 |
rs191016980 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:768524 | TAGACACTATGGTTT[A/C]TGCCATTATAAATGT | 7525 |
rs191021390 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:789994 | ACCAGGGAGGTTGAG[A/G]ATGCAGTGAGCTGAG | 7525 |
rs191035042 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:750455 | GGCTGCTGTGTGCGT[G/T]TTAAGATATTTACCA | 7525 |
rs191039075 | snp | C/T | 6.59022e-05 | 0.00573993 | intron-variant | YES1 | GRCh38.p7 | 18:732805 | AAGCCACTCATGAGA[C/T]AACCAAGAGCTATAA | 7525 |
rs191094566 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:796714 | AGTGAGCCAAGATGG[C/T]ACCACTGCACTGGCC | 7525 |
rs191138448 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:814089 | GTCACCTACAAGTTA[C/T]GGATTACATTGACTT | 7525 |
rs191140932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:777526 | AATTACTTATATCAG[A/G]CCGGGTGCATTGGCT | 7525 |
rs191150279 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:772903 | CTGTTTCTGAGTTTG[C/T]ATTTGCATGGCCAAG | 7525 |
rs191172469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:737165 | AGATTTCAAAAATCT[A/G]ACACTGGCTGGGTGC | 7525 |
rs191256574 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:764764 | TTGAGACGGAGTCTC[A/G]TTCTGTCACCCAGGC | 7525 |
rs191266796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:746513 | TAAGGTTTTGTGAAT[A/G]AAATGACAGTGTCTG | 7525 |
rs191278817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:729276 | ATTTGAGGGCCAGGC[A/G]GGGTGGCTCACGCCT | 7525 |
rs191394306 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:795886 | GTAACAAACCTGCAC[A/G]TTCAGCACATGTATC | 7525 |
rs191398597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:757230 | AAAGTATCGCTGGGC[A/G]CAGTGGCTCACGCCT | 7525 |
rs191439843 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | YES1 | GRCh38.p7 | 18:788771 | CTAAAAATATTTTTT[A/T]AAAAATTAGCCAGAC | 7525 |
rs191521791 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:743834 | TCGCATGAACCCAGG[A/T]GGCAGAGGTTGCAGT | 7525 |
rs191521938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:762247 | ATCGCTTGAACCCAG[A/G]AGGCAGAGGCTGCGG | 7525 |
rs191537520 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:725841 | GTGAGCCGAGATTGC[A/G]CCATAGCACTCCAGC | 7525 |
rs191670394 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:806966 | TCAGTAGATAGTAGT[A/G]GTAAAAGTAAGGACA | 7525 |
rs191679728 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:804957 | AGCATAGTAGTATAA[A/C]TGTTTGCTTAATTAG | 7525 |
rs191702923 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | YES1 | GRCh38.p7 | 18:767498 | TTCTCCTAGTACAAT[C/T]TGTTGAAAAACCTAT | 7525 |
rs191712292 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:764383 | ATGTGCCACCATGCC[C/T]GGCTAATTTTGTATT | 7525 |
rs191720400 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:732640 | TGTCAAGGATCGTGG[A/C]TTTCACTGACTTACC | 7525 |
rs191723180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:728948 | GTTTAATTTTCTTGT[C/T]TGAGGTTCACTTAAT | 7525 |
rs191730332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:785621 | AGCTTAATCCACAAT[A/G]CAACAGTGTTGAGAG | 7525 |
rs191735641 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:806235 | TAACTTGGACTTTCT[G/T]CACTAAAATAGTACA | 7525 |
rs191738975 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | YES1 | GRCh38.p7 | 18:765029 | GTGAGCCACCTCGCC[C/T]GGCTTATCTGAATCT | 7525 |
rs191757634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:747075 | TAACAGTCATATAAA[A/G]CTAACTGAAAGTAAT | 7525 |
rs191940832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:808063 | TACCTCAACAGTACA[C/T]TATTCTATACTCTAA | 7525 |
rs191948874 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:803148 | ACCAAGGTGGGAGGA[C/T]CACTTGAACCTGGGA | 7525 |
rs191957536 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:762700 | CAAAACCTCAGAATT[C/T]ACCACTACATAATTC | 7525 |
rs191962000 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:780813 | TTATTGCAAAAGCCT[A/C]TTTAACTGACTTCCA | 7525 |
rs191966630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:744438 | TCTGTCGCCCAGGAT[A/G]GAGTGCAGTGGTGTG | 7525 |
rs191977013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:739556 | TCTTCAAGCACGGAG[C/T]TATCAGTGCACCACT | 7525 |
rs191980922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:783935 | TTTTTCATGTTATTA[A/G]TATTTGTAACATGCA | 7525 |
rs192014064 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:746275 | TATATTAACTACTCA[A/G]TGTGTCTCTCAAAAC | 7525 |
rs192149816 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | YES1 | GRCh38.p7 | 18:757308 | GGAGATTGAGACCAT[C/T]CTGGCTAACACGGTG | 7525 |
rs192176188 | snp | C/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722736 | AGAATAAGTTTTCCT[C/G]CCCAAATCAACCATT | 7525 |
rs192177480 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:796284 | AATTTAACCTCTTGA[A/G]GCCTATTTCTTTATC | 7525 |
rs192196893 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:774125 | CTTAAGCCACGGCGC[C/T]TGGCCTTCCCATCTG | 7525 |
rs192209586 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | YES1 | GRCh38.p7 | 18:757278 | GGAGGCCAAGGCGGG[C/T]GGATCACGAGGTCAG | 7525 |
rs192209910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:737909 | TTTTTTTGTAGAGAT[A/G]GGGTTTCACTATGTT | 7525 |
rs192224474 | snp | C/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722061 | ATATAAGGAACTGCT[C/G]CATTCAGTTAAAACC | 7525 |
rs192320794 | snp | A/G | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723234 | ACAAATACCCATTTA[A/G]TGTGTAAGAAAAATT | 7525 |
rs192383882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:802829 | GGCTCACACCTATAA[C/T]CCTAGCACTTCGGGA | 7525 |
rs192421984 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:792759 | TGAGGCCAGGAGTTC[A/G]AGATCAGCCTGGGCA | 7525 |
rs192429710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:810074 | ATCACTTAAAAAATT[A/G]TTTTGGCATTAGTCT | 7525 |
rs192435458 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | YES1 | GRCh38.p7 | 18:770149 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 7525 |
rs192453209 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:753901 | CTATCTAAGTAAATG[A/G]CCCTACCATCTAATC | 7525 |
rs192460521 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:734800 | CAGTATGGAAACTCC[C/T]TAAAGAACGAAAAGC | 7525 |
rs192539174 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775453 | TCTTAACCATTACCT[G/T]GACTTCTAACATTAC | 7525 |
rs192543870 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:738185 | TTCTGAATTGTCAGA[G/T]TCTGTGGACATTTGG | 7525 |
rs192646383 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776012 | AATGACAGCAATGAA[C/T]ATTCCCGAGCCCTCC | 7525 |
rs192757969 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:779783 | ATTACAGTAAACAAT[C/T]AGATACCACTTTCAA | 7525 |
rs192813776 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:792590 | GTGTGTGTGTGTATA[C/T]ACATATATACATATA | 7525 |
rs192817876 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:752769 | TCAACAGGGCGAAAC[C/T]CTGTCTGTACTAAAA | 7525 |
rs192818080 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:726979 | CAATGGATCGGTCCA[C/T]GCTACATGTGGAAAG | 7525 |
rs192871230 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:796967 | AGTATAGAGCTAAAT[A/G]ACTTGTAAGACAAAA | 7525 |
rs192887237 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | YES1 | GRCh38.p7 | 18:757371 | AGCCGGGCGTGGTGG[C/T]GGGCGCCTGTAGTCC | 7525 |
rs192898971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:729888 | CCTTGGCTTCCCAAT[A/G]TGTTGGGATTACAGG | 7525 |
rs192928641 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:806597 | TATTTATTGTGCTAA[C/G/T]GGCTGTTCTCAAAGA | 7525 |
rs192943966 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:765183 | AGAGTTGGGAATACC[C/T]CCATAGATACGAAAA | 7525 |
rs192952478 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:731024 | TTGTTTCATGAAGGG[A/G]GTGAGAAGCAGGAAA | 7525 |
rs193014296 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:808986 | AAGAATTACTGTTCT[A/G]GAAAACCGAAAATAG | 7525 |
rs193027735 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:769563 | GCTGTAGGATTTTTG[C/T]ATTATAGCAGAACTT | 7525 |
rs193029850 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:734431 | GAGCTTGGTGGCAGG[C/T]ACCTGTAGTCCCAGC | 7525 |
rs193079845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:779086 | CTGATATAGGATCAG[C/T]CATGAGAAGAGCCTG | 7525 |
rs193091140 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:743475 | TAAGGGGCATATAGT[A/G]TATCAATGTTTTAAG | 7525 |
rs193172593 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:786106 | TTCTTTATAAATTAC[C/T]AAATCTGTGGTACTG | 7525 |
rs193174526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:747325 | AATACAAAAATTAGC[C/T]GGGCGTGGTGGTGCA | 7525 |
rs193244100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:802191 | GAGTTCGAGGCTGTA[A/G]TGAGCTATGATCATG | 7525 |
rs193244440 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:761294 | AAAAGTCGGTACAAG[A/G]AATTTACAAAATTAC | 7525 |
rs193249421 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:725592 | TAGGTACTGTCATCT[C/T]CATAAGTGAAATCTG | 7525 |
rs199503037 | in-del | -/T | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:814132 | TCCCTTTTTTTTTTT[-/T]ATTACTACATTCCCT | 7525 |
rs199522895 | snp | A/G | | | synonymous-codon | YES1 | GRCh38.p7 | 18:756669 | GGAAAGACTGCTGAA[A/G]TTAACTGCTGTTCCC | 7525 |
rs199524663 | in-del | -/A | 0.0107246 | 0.0724382 | intron-variant | YES1 | GRCh38.p7 | 18:797462 | AGGAAAAACAAAACC[-/A]AAAAAAAAACACAGG | 7525 |
rs199529011 | in-del | -/CGTCCCTTTT | | | intron-variant | YES1 | GRCh38.p7 | 18:727228 | TTTATTATTATGAAA[-/CGTCCCTTTT]TGTCCCTAGTACTAT | 7525 |
rs199539110 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:731777 | TCGAGACCATCCTGG[C/T]TAACACGGTGAAACC | 7525 |
rs199568212 | snp | A/C | 9.88631e-05 | 0.00703006 | intron-variant | YES1 | GRCh38.p7 | 18:732790 | AATAAACTCCTGATA[A/C]AGCCACTCATGAGAT | 7525 |
rs199572255 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:764915 | TTTTTTGTGTATTTT[C/T]AGTAGAGACCGGGTT | 7525 |
rs199574072 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:771005 | AGAGATATCCCATCT[A/C]AAAAAAAAAAAAAAA | 7525 |
rs199633079 | in-del | -/T | 0.242775 | 0.249896 | intron-variant | YES1 | GRCh38.p7 | 18:734404 | TAAAAATACAAAAAA[-/T]AAAAATTAGCCGAGC | 7525 |
rs199636390 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon, intron-variant | YES1 | GRCh38.p7 | 18:732919 | TATTGTAAACCGACC[A/G]TACAGTGCAGCTTCA | 7525 |
rs199707539 | snp | G/T | 0.000399281 | 0.0141238 | missense | YES1 | GRCh38.p7 | 18:736830 | TGCTGTGTATTCATT[G/T]TCTTCAATTAACCTT | 7525 |
rs199738990 | snp | A/C | 0.000774191 | 0.0196595 | intron-variant | YES1 | GRCh38.p7 | 18:748065 | GTAGACTATTGCCCA[A/C]GGTACAATATATTGC | 7525 |
rs199777688 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:727600 | TTTTTGTCTTCTCTT[C/G]TTATTTTAGTAGTTA | 7525 |
rs199803701 | snp | C/T | 0.465996 | 0.12588 | intron-variant | YES1 | GRCh38.p7 | 18:783620 | ATCAATTTTTCTCTT[C/T]TTTTTTTTTTTTTGA | 7525 |
rs199816126 | in-del | -/AC | | | intron-variant | YES1 | GRCh38.p7 | 18:783412 | CACACACACACACAC[-/AC]GGAAAAAATAATCAC | 7525 |
rs199822485 | snp | C/T | 0.000148313 | 0.00861014 | missense | YES1 | GRCh38.p7 | 18:743371 | TCTGAGGTTTCACAG[C/T]TGGACACACAGTTGT | 7525 |
rs199902979 | snp | C/T | | | missense | YES1 | GRCh38.p7 | 18:756791 | GTCTGTATTTAATGG[C/T]TGGACTTTTGTTTTC | 7525 |
rs199903309 | snp | C/T | | | missense | YES1 | GRCh38.p7 | 18:743286 | TCGCCGAAACATCCT[C/T]GTCCTAGTTTAACCT | 7525 |
rs199938938 | in-del | -/ATGTTCTG | | | intron-variant | YES1 | GRCh38.p7 | 18:782002 | TAGAACCAGCAACCC[-/ATGTTCTG]GAAATTTGGTTCATT | 7525 |
rs199969306 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:730375 | TTTGAGACAGGGTCT[C/T]GCTCTGTTGCCCAGG | 7525 |
rs200058716 | snp | C/T | 3.29468e-05 | 0.00405861 | missense | YES1 | GRCh38.p7 | 18:756590 | ATGAACTTGGCACCA[C/T]TGAAAATGAGGAAGA | 7525 |
rs200091393 | in-del | -/C | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813658 | ACGATGCTGTATTTT[-/C]CTTAGCTACTAAAAC | 7525 |
rs200128954 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:777317 | GTTGGAAAAATAAAC[C/T]ACTGAATTGTAACTT | 7525 |
rs200135493 | in-del | -/A | 0.130008 | 0.219321 | intron-variant | YES1 | GRCh38.p7 | 18:751859 | AACTTAACAAAACAG[-/A]AAAAAAGAACTATTG | 7525 |
rs200158425 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:733684 | GCTACTCGGGAGGCT[G/T]AGGCAGGAGAATGGT | 7525 |
rs200270227 | snp | C/T | | | synonymous-codon | YES1 | GRCh38.p7 | 18:747940 | TGCCTGAATGGAATC[C/T]GCAGGCGCTACATAA | 7525 |
rs200295029 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:743920 | CGAAAAAAAAAAAAA[-/T]ATATATATATATACA | 7525 |
rs200295967 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:805971 | GGCTGAAAACCAGAC[A/G]ATCTTGAAGTTTCAG | 7525 |
rs200305028 | in-del | -/AA/TA | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722009 | AAATGAATACACATT[-/AA/TA]AAGTTAGTGTTTTAT | 7525 |
rs200323097 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:761243 | TGTTCTTTGCCGTTT[-/A]AAAAAAAAAAAAAAA | 7525 |
rs200430116 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:736335 | TCTGTTGTGGGGGGA[A/G]GGGGGGGTTTGCCTG | 7525 |
rs200469547 | in-del | -/A | 0.0103295 | 0.0711199 | intron-variant | YES1 | GRCh38.p7 | 18:769664 | TTTCTACATGTACTT[-/A]AGATTATCATATAGG | 7525 |
rs200469944 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:803438 | AGAGAAGGTAAAGAA[G/T]TTACAAACTCCATAT | 7525 |
rs200496737 | in-del | -/AGG | 0.0134861 | 0.0810011 | intron-variant | YES1 | GRCh38.p7 | 18:731251 | AAGACAAGATTACAC[-/AGG]AGAAGAGTTCAAGCT | 7525 |
rs200522471 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:744429 | GAGTCTCACTCTGTC[A/G]CCCAGGATGGAGTGC | 7525 |
rs200545548 | snp | C/T | 0.000280013 | 0.0118291 | synonymous-codon, intron-variant | YES1 | GRCh38.p7 | 18:732835 | AAATGCAAGCTTACC[C/T]GGATATGGCACTCGG | 7525 |
rs200573604 | in-del | -/A | 0.307423 | 0.243316 | intron-variant | YES1 | GRCh38.p7 | 18:802545 | GTGAAACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 7525 |
rs200594254 | snp | C/T | 0.000658707 | 0.0181361 | missense | YES1 | GRCh38.p7 | 18:756653 | CTCCAAATGGTGTCA[C/T]GGAAAGACTGCTGAA | 7525 |
rs200601157 | snp | C/T | 0.000131907 | 0.00812009 | intron-variant | YES1 | GRCh38.p7 | 18:732981 | CTAAAATAATGTTGA[C/T]CATCTTGCTTAATTG | 7525 |
rs200613073 | snp | C/T | 3.41413e-05 | 0.00413153 | intron-variant | YES1 | GRCh38.p7 | 18:739724 | ATGGATACATGTATA[C/T]ATACAGATACCTGAG | 7525 |
rs200702832 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:742462 | CCAGTCTCTATTTAA[A/T]AAAAAAAAAAAAAAG | 7525 |
rs200706321 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:791262 | AGAAGAAAAAAAAAA[A/G]AAAAAAAAAAAAGAA | 7525 |
rs200714782 | snp | C/T | | | missense | YES1 | GRCh38.p7 | 18:756713 | ACGGACATGGTGACA[C/T]TGTAGTGGGTTCTGC | 7525 |
rs200760371 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:733280 | ATGTGTAACTTTTAA[G/T]TACAGTCTGGCACCT | 7525 |
rs200762886 | snp | G/T | 0.00199792 | 0.0315431 | synonymous-codon | YES1 | GRCh38.p7 | 18:736815 | AATTTTACCTTGTCT[G/T]GCTGTGTATTCATTG | 7525 |
rs200788821 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:759703 | GGAGACAATTTATTT[A/T]TTTCTTTTTTTCTTT | 7525 |
rs200792698 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:748360 | ACTCAGTATTCTTTT[C/T]TTTTTTTTTTTTTTA | 7525 |
rs200806325 | in-del | -/A | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:792263 | AGCTGAGATTGTGCC[-/A]ACTGTACTCCAGCCT | 7525 |
rs200839210 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:732371 | CTTGAACCCGGGAGA[C/G]AGGTTGCAGTGAGCC | 7525 |
rs200860807 | snp | C/T | | | missense | YES1 | GRCh38.p7 | 18:756623 | CACCTCCAAAAGGCG[C/T]TACCCCTGAGGATCC | 7525 |
rs200885771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:743250 | GAAAACAAAAATTCA[A/G]GCTTCTTACCCATCC | 7525 |
rs200888546 | in-del | -/AAAAAACAAAA | 0.0119091 | 0.0762411 | intron-variant | YES1 | GRCh38.p7 | 18:799904 | CAAACAAACAAAAAC[-/AAAAAACAAAA]AAAAAAGAAGGTATG | 7525 |
rs200917511 | snp | A/T | 0.000532012 | 0.016301 | intron-variant | YES1 | GRCh38.p7 | 18:724650 | AATACACAAGATTAA[A/T]ACATTAAAGAACAAT | 7525 |
rs200955379 | in-del | -/T | 0.120326 | 0.21374 | intron-variant | YES1 | GRCh38.p7 | 18:759611 | AAATAACGTACAGAC[-/T]TTTTTTCCTTGTCAT | 7525 |
rs200975694 | in-del | -/ATG | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:778336 | GAAAATGTAACAAAC[-/ATG]ATAACATTATTTACA | 7525 |
rs200994862 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:742213 | TACCATCTGCACAGG[A/G]AAAAAGAGGAAAGAG | 7525 |
rs201017610 | in-del | -/CTTGAAGAAG | | | intron-variant | YES1 | GRCh38.p7 | 18:791242 | CCAACAAGAGTGAAA[-/CTTGAAGAAG]AAAAAAAAAAGAAAA | 7525 |
rs201031432 | snp | A/T | 0.0479149 | 0.147179 | intron-variant | YES1 | GRCh38.p7 | 18:743920 | CGAAAAAAAAAAAAA[A/T]ATATATATATATACA | 7525 |
rs201035778 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:736211 | ATTACAGATAGGAAG[A/G]CATTCCAGATGGAGG | 7525 |
rs201064218 | in-del | -/G/GG | | | intron-variant | YES1 | GRCh38.p7 | 18:756291 | TACAGTGGGGGGGGG[-/G/GG]CTCAATAACTATTTG | 7525 |
rs201078508 | snp | C/G | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722368 | CATGAAGTCCATCTT[C/G]ACATTTTAAAAATGG | 7525 |
rs201135512 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:779924 | TTTTTTTTTTTTTTT[C/T]TTAAATCTCTTTAAG | 7525 |
rs201205204 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | YES1 | GRCh38.p7 | 18:745964 | TTTAGTTGTTTCACT[C/T]TCTCTTACTAAGAAA | 7525 |
rs201294724 | snp | A/C | 1.64732e-05 | 0.0028699 | synonymous-codon | YES1 | GRCh38.p7 | 18:756603 | CACTGAAAATGAGGA[A/C]GATGCACCTCCAAAA | 7525 |
rs201363426 | in-del | -/GCTTA | | | intron-variant | YES1 | GRCh38.p7 | 18:769421 | TACGTCTTTTTCCCT[-/GCTTA]CCTTATTCACTGACT | 7525 |
rs201413906 | snp | A/G | 0.000330775 | 0.0128561 | synonymous-codon | YES1 | GRCh38.p7 | 18:736899 | TCCTACAAGAATATT[A/G]GCAGCCCGAAGATCT | 7525 |
rs201459970 | in-del | -/G | | | intron-variant | YES1 | GRCh38.p7 | 18:792868 | AAGCCAAGGGGGGGG[-/G]AAAAAGCTTAAATCA | 7525 |
rs201471772 | snp | C/T | 0.000312935 | 0.0125048 | synonymous-codon | YES1 | GRCh38.p7 | 18:756681 | GAAATTAACTGCTGT[C/T]CCCTTTGCTGAAGAT | 7525 |
rs201472161 | snp | A/G | | | missense, intron-variant | YES1 | GRCh38.p7 | 18:732923 | GTAAACCGACCATAC[A/G]GTGCAGCTTCAGGAG | 7525 |
rs201523600 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:730959 | CAGAGAAGGGTGAAA[A/T]CAGCAAAGGAGTGAT | 7525 |
rs201559016 | in-del | -/T | 0.039522 | 0.134904 | intron-variant | YES1 | GRCh38.p7 | 18:751335 | ACTTTCTCCCCCTCC[-/T]TTTTTTTTTAATAGA | 7525 |
rs201651859 | snp | C/T | 1.6795e-05 | 0.0028978 | missense | YES1 | GRCh38.p7 | 18:743068 | GTTTTAGTGTTTTGA[C/T]TGCTACTTTCGTGGT | 7525 |
rs201705322 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:792565 | TCTCTCCCTCTGTAT[A/G]TGTGTGTGTGTGTGT | 7525 |
rs201714713 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:743915 | GACTCGAAAAAAAAA[-/T]AAAATATATATATAT | 7525 |
rs201761609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:785825 | ACCAGTAGTCCCAGC[C/T]ACTTGGGAGGCTGAA | 7525 |
rs201777329 | in-del | -/G | 0.0178098 | 0.0926698 | intron-variant | YES1 | GRCh38.p7 | 18:786377 | AAGAGTGTCAAGTTT[-/G]AGGGACACTGGCAAG | 7525 |
rs201802922 | in-del | -/ATT | 0.0178098 | 0.0926698 | intron-variant | YES1 | GRCh38.p7 | 18:793026 | TTAAGGTTCATTATA[-/ATT]ATTATTATTATTATT | 7525 |
rs201867903 | in-del | -/AGG | 0.243347 | 0.249911 | intron-variant | YES1 | GRCh38.p7 | 18:734464 | TCGGGAGGCTTAGGC[-/AGG]AGAATGGCGAGAACC | 7525 |
rs201882590 | snp | C/T | 0.000399281 | 0.0141238 | missense | YES1 | GRCh38.p7 | 18:739746 | ATACCTGAGCAGCCA[C/T]ATCAACCAGCTGTGG | 7525 |
rs201911630 | snp | A/G | 1.71628e-05 | 0.00292935 | intron-variant | YES1 | GRCh38.p7 | 18:743437 | AAATGAATAAACTAT[A/G]CTGTAATATCAATTA | 7525 |
rs201965280 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:804928 | CAAAAAAAAAAAACA[G/T]AAACCAAAAACCTAG | 7525 |
rs201966473 | snp | C/T | 0.000592846 | 0.0172067 | missense | YES1 | GRCh38.p7 | 18:756629 | CAAAAGGCGTTACCC[C/T]TGAGGATCCTCCAAA | 7525 |
rs201983339 | snp | A/C | | | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721562 | ACAAAACAAAACAAA[A/C]AAAAAAGAAAATTGA | 7525 |
rs201988709 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:742463 | CAGTCTCTATTTAAA[A/T]AAAAAAAAAAAAAGA | 7525 |
rs201997522 | in-del | -/A | 0.0103295 | 0.0711199 | intron-variant | YES1 | GRCh38.p7 | 18:802921 | CCCTGTCTCTATTCT[-/A]AAAAAAAAATAAAAA | 7525 |
rs202041681 | in-del | -/CAAACATTACAGATAGGAAG | | | intron-variant | YES1 | GRCh38.p7 | 18:736191 | AAACAACAACAACAA[-/CAAACATTACAGATAGGAAG]GCATTCCAGATGGAG | 7525 |
rs202050703 | snp | A/G | 4.96553e-05 | 0.00498249 | synonymous-codon | YES1 | GRCh38.p7 | 18:745726 | TGTAGTGTTTCACCA[A/G]TTTCTGCAGAGTATC | 7525 |
rs202056485 | snp | A/G | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723398 | TAAAACTTTCACTTT[A/G]TTTTCTCGTATTTCT | 7525 |
rs202083013 | snp | C/T | 9.88338e-05 | 0.00702902 | missense | YES1 | GRCh38.p7 | 18:747987 | CATTCTTTCCTGTAG[C/T]GATTGATCTTGCTTC | 7525 |
rs202136846 | in-del | -/AAG | 0.00716266 | 0.059414 | cds-indel | YES1 | GRCh38.p7 | 18:724333 | AAAACATGCAGAGTA[-/AAG]AAGATTTTCTTCTTT | 7525 |
rs202142373 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:756857 | AGACAATAAAATATT[C/T]TGAGAGTCAGTTAAC | 7525 |
rs202188142 | snp | C/T | 0.000543456 | 0.0164752 | missense | YES1 | GRCh38.p7 | 18:756733 | GTGGGTTCTGCTCCA[C/T]AATGGCTCACACTTG | 7525 |
rs202188889 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:730370 | TTTTTTTTGAGACAG[A/G]GTCTTGCTCTGTTGC | 7525 |
rs367550558 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:784525 | ATACAAACGTATTTA[A/T]CTTACAGTTCAGAAG | 7525 |
rs367569942 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:772318 | ACAGGCATGAGCCAC[C/T]GCACCCGGCCTGCAT | 7525 |
rs367586890 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:737902 | GTTTGTATTTTTTTG[C/T]AGAGATGGGGTTTCA | 7525 |
rs367596548 | snp | C/T | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723008 | GAGGCAGGAGAATGG[C/T]GTGAACCTGGGAGGC | 7525 |
rs367611992 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:756974 | CAAAAAATAGAAAGC[A/T]GAAAACGAGGTCTCT | 7525 |
rs367703228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:726286 | AAAAATTAGCTGGGC[A/G]TGGTGGTGGGCATCT | 7525 |
rs367724548 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:750772 | TTGAGAAAGGACATA[G/T]TAACTATATTTTGAA | 7525 |
rs367733542 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:740009 | TTTTGAAAACTTCTG[A/G]TAACACATGCAAAAA | 7525 |
rs367771368 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:769116 | CCATATAGCCTAGGT[A/G]TATAGGTATATAGGT | 7525 |
rs367772146 | snp | A/G | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775814 | ATAAATTAAAAAAAA[A/G]AATAGAATCATATAT | 7525 |
rs367776230 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:734935 | AGCCAAGGCGTGTGG[A/G]TCACCTGAGGTCAGG | 7525 |
rs367847824 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | YES1 | GRCh38.p7 | 18:739856 | AATAAGCAAATCTTA[C/T]ATTAGGATTGAAATG | 7525 |
rs367849921 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:811933 | CAGGTAGCGCGGGGA[A/T]CGAGACAAGCCCGCC | 7525 |
rs367901773 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:783153 | TACTCAGGAGGCCAA[C/G]GCAGAGGATCACTTG | 7525 |
rs367948752 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:793122 | TGGGCTCACTGCAAC[A/C]TCCACCTCCCGGGTT | 7525 |
rs367966762 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:738419 | ATTCAGGCCAGGTGC[A/G]GTGGCTCACGCCTGT | 7525 |
rs367974335 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:772117 | CACGGCAACCTCTGC[C/G]TCCTGGGTTCAAGTG | 7525 |
rs367983656 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:782787 | GCAACCTCCACCTCC[A/T]GGGTTCAAGTGATTC | 7525 |
rs368000027 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:747230 | ATCCTAGCACTTTGG[A/G]AGGCTGAGGCGGGTG | 7525 |
rs368034931 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:809454 | ACAGGGGCGCGCCAC[A/C]ACACCCAGATAATTT | 7525 |
rs368045451 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:764339 | GTGATTCTCCTGACT[A/C]AGCCTCCCAAGTAGC | 7525 |
rs368077669 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:733900 | ATATGTGTTTGTAGA[C/T]AGTGTTTTAAAACAG | 7525 |
rs368083653 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:751085 | TTTATGTTCCGGAAC[A/G]ATAACTGGTAGCAGA | 7525 |
rs368097788 | snp | C/T | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776573 | CTTTAATTTTCTGTG[C/T]ATTGGAGGAGTAGGA | 7525 |
rs368099773 | snp | C/T | 1.65375e-05 | 0.0028755 | missense | YES1 | GRCh38.p7 | 18:724632 | TCACGGTTCACCATA[C/T]CTAATACACAAGATT | 7525 |
rs368125075 | snp | C/T | 0.0134861 | 0.0810011 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723016 | AGAATGGTGTGAACC[C/T]GGGAGGCAGAGCTTG | 7525 |
rs368141940 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:759866 | CTTCCCCCCTCCCCC[C/T]ACCCCACGACAAGCC | 7525 |
rs368195770 | in-del | -/GACT | | | intron-variant | YES1 | GRCh38.p7 | 18:773770 | ATCTGATCCAATGCT[-/GACT]AATAAAAGAAAAAAA | 7525 |
rs368233660 | snp | G/T | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776626 | CCCCAGAACCTAGAA[G/T]ACAGTCTGAAACATA | 7525 |
rs368282558 | in-del | -/C | | | intron-variant | YES1 | GRCh38.p7 | 18:737476 | TAAAACCTAACATTA[-/C]TCTGAAGACCAAGAT | 7525 |
rs368354978 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:745321 | TTAGGAAAGCTTATG[C/T]GATCCAGCCCATGCA | 7525 |
rs368359672 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:763928 | AGATCGAGACCATCC[C/T]GGCTAACAGGGCGAA | 7525 |
rs368364814 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | YES1 | GRCh38.p7 | 18:782684 | TAAAAAGGATTATTT[G/T]TTCTTTCTAATTTTA | 7525 |
rs368365271 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:731837 | CTGGGCGTGGTGGCG[G/T]GTGCCTATAGTCCTA | 7525 |
rs368384226 | in-del | -/CAAAAAAAAAA | | | intron-variant | YES1 | GRCh38.p7 | 18:799910 | AACAAAAACAAAAAA[-/CAAAAAAAAAA]GAAGGTATGATTGCT | 7525 |
rs368399903 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:772977 | CTGCTGACCAGTTAT[A/G]GTTTGGCTATAGGCT | 7525 |
rs368404804 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:764803 | AGTGGCGCGATCTCG[A/G]CTCACTGTAACCTCC | 7525 |
rs368410214 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:748449 | CTAGTTTTTAATATA[C/T]TTACAGAGTTGTACA | 7525 |
rs368444834 | snp | C/T | 1.84221e-05 | 0.00303492 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724387 | ACAAGTTCTTTATAT[C/T]TTGGCAGATTTGTGC | 7525 |
rs368508541 | snp | C/T | 1.65548e-05 | 0.002877 | splice-donor-variant | YES1 | GRCh38.p7 | 18:751704 | TATTCATGACACTTA[C/T]GTATTGTTAATTATT | 7525 |
rs368519340 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:757285 | AAGGCGGGCGGATCA[C/T]GAGGTCAGGAGATTG | 7525 |
rs368534424 | snp | C/T | 0.000153988 | 0.00877328 | missense | YES1 | GRCh38.p7 | 18:751757 | ATGAAAGGTCTTCTG[C/T]AGTTCTAGCTTCATA | 7525 |
rs368550202 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | YES1 | GRCh38.p7 | 18:736778 | AAAACACACAACACA[C/T]TACAAGCTTTTATGT | 7525 |
rs368556407 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:773251 | TCCAGCTCTACTAAG[C/T]CACCTGCCATTACCA | 7525 |
rs368561771 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:729214 | TCTATTATGCCCATC[G/T]AGTGAGTACTTAATT | 7525 |
rs368594401 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:777845 | AAAAAAGAATTACCT[A/G]TATCAGAACATACTT | 7525 |
rs368599466 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:762936 | ATGTACAAAATACCA[C/T]GGAAATACAACAAAT | 7525 |
rs368605196 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:743500 | TTTAAGTTTAAACTG[C/T]AGAAAAACAAAAACA | 7525 |
rs368609827 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:727860 | CTTCCCTGGCTTCCA[C/T]ATCTGAGGAAAAGTT | 7525 |
rs368612869 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:741094 | GCAGAGACGGGGTTT[C/T]GCTATGTTGGCCAGG | 7525 |
rs368623922 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:760123 | ACTGAGGGACATCTG[A/G]GTTGGTTCCAAGTCT | 7525 |
rs368625681 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:749817 | GTGAGCCGAGATTGC[A/G]CCACTGCACTCCAGC | 7525 |
rs368674281 | snp | C/T | 0.00031295 | 0.0125051 | synonymous-codon, intron-variant | YES1 | GRCh38.p7 | 18:732940 | TGCAGCTTCAGGAGC[C/T]GTCCATTTGATTGGA | 7525 |
rs368758154 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:791122 | GGGCGTGGTGGTGCG[C/T]GTTTGTAATCCCAGC | 7525 |
rs368793073 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:742473 | TTAAAAAAAAAAAAA[A/G]AAAGAAAGCAGTGGG | 7525 |
rs368803356 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:759002 | TAGGTGAGTGTTGGC[C/T]GCCTCATAAATTCTG | 7525 |
rs368807660 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:787362 | CCTCGGCCTCCCAAA[A/C]TGCTGGGGTACAGGC | 7525 |
rs368812552 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:740600 | TGAAAACAAAGAGCA[A/G]AACAGTGGGTTTATG | 7525 |
rs368845120 | snp | A/G | 4.94931e-05 | 0.00497434 | synonymous-codon | YES1 | GRCh38.p7 | 18:743273 | ACCCATCCACACTTC[A/G]CCGAAACATCCTTGT | 7525 |
rs368910520 | in-del | -/G | 0.0126979 | 0.078662 | intron-variant | YES1 | GRCh38.p7 | 18:743666 | TAATCCCAGCACTTT[-/G]GGAGGTTGAGGCAGA | 7525 |
rs368921388 | snp | G/T | 7.53452e-05 | 0.00613734 | intron-variant | YES1 | GRCh38.p7 | 18:742869 | CATACAAATCAAGAC[G/T]CTTAAAAACATTATC | 7525 |
rs368966522 | snp | A/G | 0.000381524 | 0.0138064 | intron-variant | YES1 | GRCh38.p7 | 18:733017 | TAAAAATCTATTTGT[A/G]TAAACATAGCATATG | 7525 |
rs368980329 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:798711 | ACCAGTGCGCTTCCT[A/C]ACCTTTCATATAAGA | 7525 |
rs368984468 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:757249 | TGGCTCACGCCTGTA[A/G]TCCCAGCACTTTGGG | 7525 |
rs368992803 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:779305 | GCTACTCAGAAGGCT[A/G]AGGTGGGAGGACAGC | 7525 |
rs369049316 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:763520 | GGCGTCATGGCAGAA[C/T]CCCGTCTCTACAAAA | 7525 |
rs369096255 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:774650 | TTCTCTCCACCTCCC[A/T]CTGCTACCCTGGTCT | 7525 |
rs369099687 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:794472 | TTTTTGTTATAAAGA[A/T]TATTATTAGGACAAT | 7525 |
rs369135022 | snp | C/T | 0.000110805 | 0.00744247 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724384 | TACACAAGTTCTTTA[C/T]ATTTTGGCAGATTTG | 7525 |
rs369138745 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:770987 | TCTGCTCTGGGCAAT[-/T]GAAGAGATATCCCAT | 7525 |
rs369174686 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:759495 | ACAAAAACCCATAAC[C/T]GGATCTGGAAACTTA | 7525 |
rs369188135 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:728256 | ACCTGAGCCCAGGGA[A/G]GTAGAGGCTGCAGTG | 7525 |
rs369214671 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:744824 | TCCACATGCCTAACA[A/G]GAGACTGATTTTTTT | 7525 |
rs369259570 | in-del | -/AC | | | intron-variant | YES1 | GRCh38.p7 | 18:786497 | CATTAATAAGTCCAT[-/AC]ACACACACACACACA | 7525 |
rs369352035 | in-del | -/TGTG | | | intron-variant | YES1 | GRCh38.p7 | 18:792566 | CTCTCCCTCTGTATA[-/TGTG]TGTGTGTGTGTGTGT | 7525 |
rs369404569 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:808010 | ATTTGGGGGGGAAAA[A/G]GAGTTGAGGCACAGA | 7525 |
rs369445166 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:764770 | CGGAGTCTCGTTCTG[C/T]CACCCAGGCTGGAGT | 7525 |
rs369460488 | in-del | -/TTAT | 0.0236746 | 0.106192 | intron-variant | YES1 | GRCh38.p7 | 18:768693 | CTATGTTTAGATATG[-/TTAT]TTATTTATTTATTTA | 7525 |
rs369468052 | in-del | -/AAAAAAAAAAGAA | 0.0115144 | 0.0749975 | intron-variant | YES1 | GRCh38.p7 | 18:791252 | TGAAACTTGAAGAAG[-/AAAAAAAAAAGAA]AAAAAAAAAAGAAAG | 7525 |
rs369560561 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:742646 | GTGTACAAACACTTT[C/G]TATTTTTCACCTTTC | 7525 |
rs369598509 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:800495 | GTTGTACTGTAGATA[C/T]TGTGGGATAATAATG | 7525 |
rs369606702 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:763761 | GGCCAGTGATAATGG[A/G]GGAAATGAGAAGTGT | 7525 |
rs369649057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:783678 | CTGGAGTGCAATGGT[A/G]CAATCTCAGCTCAAT | 7525 |
rs369670968 | snp | G/T | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775205 | TAACATAGTGGCTGG[G/T]ATTTGAAGCACGAAT | 7525 |
rs369674153 | snp | A/G | 1.65894e-05 | 0.00288 | intron-variant | YES1 | GRCh38.p7 | 18:756536 | TCAAACAGACAACAT[A/G]ATTGTCCATTTAAAT | 7525 |
rs369678010 | snp | A/G | 3.33639e-05 | 0.00408422 | intron-variant | YES1 | GRCh38.p7 | 18:724663 | AAAACATTAAAGAAC[A/G]ATGGTCCTAACTACC | 7525 |
rs369729502 | in-del | -/C | | | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721558 | AAAAACAAAACAAAA[-/C]AAAAAAAAAAGAAAA | 7525 |
rs369751218 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:729288 | GGCGGGGTGGCTCAC[A/G]CCTGTAATCTCAGCT | 7525 |
rs369751364 | in-del | -/C | 0.00835141 | 0.0640778 | intron-variant | YES1 | GRCh38.p7 | 18:752557 | ATGAATGAACAATTG[-/C]CATCTAATCATTACC | 7525 |
rs369770567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:762046 | ACAAAATTAGCTGGG[C/T]GTGGTGGTGCATGCC | 7525 |
rs369776096 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:780788 | GACTACTAATTATTT[A/T]CGGTCTGGATTATTG | 7525 |
rs369783723 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:801856 | AGGAAAAAAAGAAAC[C/T]TGATTGGGAAAACAT | 7525 |
rs369816057 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon | YES1 | GRCh38.p7 | 18:756630 | AAAAGGCGTTACCCC[C/T]GAGGATCCTCCAAAT | 7525 |
rs369895749 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:752162 | ACCCAGGCTGGAGTG[C/T]AGTGGTGTGATTTTG | 7525 |
rs369920511 | in-del | -/ATGTT | | | intron-variant | YES1 | GRCh38.p7 | 18:809059 | TGAGTTTTAATTGTC[-/ATGTT]ATGTAATTTTCAGAA | 7525 |
rs369941496 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:757319 | CCATCCTGGCTAACA[A/C/T]GGTGAAACCCCGCCT | 7525 |
rs369950289 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:770107 | TGGCAGTACAGGCAC[A/G]CGCCACCACACCCAG | 7525 |
rs369950680 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:774172 | CCTCTTGGTTTCCCC[C/G]CGTCTTACTGGCTGC | 7525 |
rs370073093 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:805451 | GGCAGAGCATGACTA[C/T]ATTGTAACAACTTCA | 7525 |
rs370121244 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812599 | CGGTGCAGGCCGAGG[C/G]GGCGTGAGGAGGAGG | 7525 |
rs370198716 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:748923 | CCCAGCACTTTGGGA[A/G]GCTGAGGCAGGCAGA | 7525 |
rs370206993 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:784517 | TTAAAACAATACAAA[C/T]GTATTTATCTTACAG | 7525 |
rs370226956 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:802227 | GCACTCCAGCCTGGG[A/C]AAACACAGCAAGACC | 7525 |
rs370235737 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:771936 | GAAGAAGGGATTTTA[C/T]TGTAAAGATAAAAAT | 7525 |
rs370316460 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:763035 | TTGAAGAGTTGGAGA[C/G/T]TTGGGGGAAAGAAAA | 7525 |
rs370321782 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:749405 | CAGGAGACTGAGGCA[A/G]GAGAATCGCTTGAAC | 7525 |
rs370382933 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:726852 | ATACTGTCAATAAAT[A/G]TAAGGATTTCATACC | 7525 |
rs370415158 | snp | C/T | 6.59087e-05 | 0.00574021 | intron-variant | YES1 | GRCh38.p7 | 18:748044 | TAAAACAGCAATCAC[C/T]GCAAGGTAGACTATT | 7525 |
rs370424560 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:782628 | TCTATGATTTTAAAT[A/C]TTATATGAATGGGAA | 7525 |
rs370426200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:742841 | AAATTAGAAAACAGT[A/G]TAAGTCTATATGCAT | 7525 |
rs370437151 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:747174 | AGTAAAACCTTAAAG[A/C]ATGTAAGTCTTTGGG | 7525 |
rs370458596 | snp | C/T | 3.29527e-05 | 0.00405898 | intron-variant | YES1 | GRCh38.p7 | 18:732796 | CTCCTGATAAAGCCA[C/T]TCATGAGATAACCAA | 7525 |
rs370471312 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:729684 | CAGGCCAGAGTGCAG[C/T]GGCGCAATCTCAGCT | 7525 |
rs370522608 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775922 | CTTTGTTTTCACTTC[C/T]GTGTAGCATTCTTTT | 7525 |
rs370573556 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:771139 | GGAGGCCCAGGCAGG[C/G]AGATCACTTGAGGTC | 7525 |
rs370573975 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:745206 | AATATTAAATACCTT[C/T]AGAGGTCCTTGAAAG | 7525 |
rs370580389 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:789845 | CAGGCAGATTGCCTG[A/C]GGTCAGAAGTTTGAG | 7525 |
rs370608070 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:740515 | ACTGGATCGGGGAAG[G/T]GTAGTTGGTGGACTG | 7525 |
rs370616801 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:731860 | TAGTCCTAGCTACTC[A/G]GGAGGCTGAGGCAGG | 7525 |
rs370674863 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:731966 | AGCGAGACTCCATTT[A/C]AAAAAAAAAAAAAAA | 7525 |
rs370701863 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:807840 | AAGAACCTATATGCC[A/G]GCAATTCTACTCCCC | 7525 |
rs370733020 | snp | A/T | 1.70258e-05 | 0.00291764 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724411 | TTTGTGCATATAAAA[A/T]AGGCTACTTGAATTA | 7525 |
rs370796909 | snp | C/T | 8.23811e-05 | 0.00641746 | synonymous-codon | YES1 | GRCh38.p7 | 18:724580 | ACAGCCCTGAGGGCA[C/T]GGCATCCTGTATCCT | 7525 |
rs370819737 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:796406 | GTCACACAGTCAATT[A/C]TCAATACACATTAGT | 7525 |
rs370834164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:736996 | AAAACACAAGACATA[C/T]GATACAAAGGGAAGC | 7525 |
rs370860706 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:738487 | CGAGGTCAGGAGATC[A/G]AGACCATCCTGGCGA | 7525 |
rs370895470 | in-del | -/CCTTA | | | intron-variant | YES1 | GRCh38.p7 | 18:769426 | CTTTTTCCCTGCTTA[-/CCTTA]TTCACTGACTAGTAC | 7525 |
rs370915676 | snp | A/G | 5.61488e-05 | 0.00529823 | intron-variant | YES1 | GRCh38.p7 | 18:756847 | AAATCTACAGAGACA[A/G]TAAAATATTTTGAGA | 7525 |
rs370920392 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:737028 | GAGAGAAGACAATTA[C/T]GGTTAATATCAAATT | 7525 |
rs370963250 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722943 | TAAAAATACAAAAAA[C/T]TAGCCAGGCGTGGTG | 7525 |
rs371084167 | in-del | -/A/AA | | | intron-variant | YES1 | GRCh38.p7 | 18:804609 | GTGAGACTGAGTCTC[-/A/AA]AAAAAAAAAAAAAAA | 7525 |
rs371095882 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:734617 | CATCACTAATCATCA[-/G]GGGAAATGCAAATTA | 7525 |
rs371185669 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:781396 | GGCACAACCTCCCTC[C/T]TTCCTTACGCTTGGC | 7525 |
rs371202088 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:746702 | TTAAGTGTTATAACA[C/T]GAAAATAAAGTAGCG | 7525 |
rs371207845 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:730635 | TGCTTTCTGTCTGGG[G/T]TTTACTGCCCTGTGC | 7525 |
rs371228082 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:774878 | TCCAATAACCTATTA[C/T]GCAGCCTTCAACTCC | 7525 |
rs371237554 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:808434 | ATACCCTACCATAGC[C/T]ATACACGAACTACCA | 7525 |
rs371244139 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:767506 | GTACAATTTGTTGAA[A/T]AACCTATCCATTTCC | 7525 |
rs371247254 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:741738 | AGCCCAGGGAGGTCC[A/G]AGCTGCAGAGAAATG | 7525 |
rs371259535 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:725621 | TGGCCGGGCACAGTG[A/G]CTCTCGTCTGTAATC | 7525 |
rs371309832 | in-del | -/C | | | intron-variant | YES1 | GRCh38.p7 | 18:804437 | CATGGTGAAACCCCC[-/C]ATCTCTACTAAAAAT | 7525 |
rs371335812 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:744072 | TAACTTAAAATATAT[A/T]TTTTTTTAAGTTATT | 7525 |
rs371352602 | snp | C/T | | | missense | YES1 | GRCh38.p7 | 18:745986 | ACTAAGAAAATACCT[C/T]GTTGATTTCCAGGAT | 7525 |
rs371384968 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:796942 | ACCTCACAACATACA[G/T]AAAATCCAGAGTATA | 7525 |
rs371390237 | snp | A/C/T | 1.65531e-05 | 0.00287686 | missense | YES1 | GRCh38.p7 | 18:751787 | AATCATATAAGGCCA[A/C/T]AAATATAGTAACACC | 7525 |
rs371392344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:771473 | TTCCTTAAAAATCAC[C/T]TTCAAATAAATTAAC | 7525 |
rs371401226 | in-del | -/CAA | | | intron-variant | YES1 | GRCh38.p7 | 18:736191 | AAACAACAACAACAA[-/CAA]ACATTACAGATAGGA | 7525 |
rs371404494 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:799640 | CCTGGGAGGTGGAGG[C/T]AGCAGTGAGCTGAGA | 7525 |
rs371413228 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | YES1 | GRCh38.p7 | 18:791120 | CCGGGCGTGGTGGTG[C/T]GCGTTTGTAATCCCA | 7525 |
rs371428140 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:757328 | CTAACACGGTGAAAC[C/T]CCGCCTCTACTAAAA | 7525 |
rs371453423 | in-del | -/AA | | | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721537 | GCGAGACTCCGTCTC[-/AA]AAAAAAAAAACAAAA | 7525 |
rs371454340 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:811648 | GAAAGGCTCATCCAC[C/T]CGCCCCACACACCCG | 7525 |
rs371500867 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:786010 | CCATGAGATAACACA[A/G]CAAGAAGAAGGCCCT | 7525 |
rs371608400 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:730283 | GGCTATTTTCTGTTA[C/G]GTCTCCCAGAGACTC | 7525 |
rs371615786 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:786941 | TCCCTCTAGGAGGAA[C/T]GGTTCAGTCTTTGAT | 7525 |
rs371620884 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:761117 | TTGACTCAATATACT[C/T]AAGCCTGAAGGCAAA | 7525 |
rs371657302 | snp | A/C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:757457 | GCAGTGAGCAGAGAT[A/C/T]GCGCCACTGCACTCC | 7525 |
rs371715517 | in-del | -/GTCAACCACT | | | intron-variant | YES1 | GRCh38.p7 | 18:748564 | CTACCTCCAACCACT[-/GTCAACCACT]AATCAGCTTTCTGTC | 7525 |
rs371749610 | in-del | -/AACAAAAC | | | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721546 | CCGTCTCAAAAAAAA[-/AACAAAAC]AAAACAAAAAAAAAA | 7525 |
rs371801369 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:749362 | AATTAGGTGGGAGTG[A/G]TGGCGTGTGCCTGTA | 7525 |
rs371847499 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:735645 | CTTGAATCTGGGAGG[C/T]GGAAGTTGCAGTGAG | 7525 |
rs371854059 | snp | C/T | 0.000153988 | 0.00877328 | missense | YES1 | GRCh38.p7 | 18:736810 | AAAGTAATTTTACCT[C/T]GTCTTGCTGTGTATT | 7525 |
rs371858197 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:727465 | ATTTAATTATGGATG[C/T]AGTTGGGTTTAATTC | 7525 |
rs371888565 | snp | A/T | 0.000131781 | 0.00811621 | intron-variant | YES1 | GRCh38.p7 | 18:732826 | AGAGCTATAAAATGC[A/T]AGCTTACCTGGATAT | 7525 |
rs371937696 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:740773 | TTGTACCCAGTGGTC[C/T]GACAACACAGAATTT | 7525 |
rs371941410 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:755359 | GTTCAAGCACTACTC[A/G]TGCCTCAGCCTCCCG | 7525 |
rs371944352 | in-del | -/TTTTG | | | intron-variant | YES1 | GRCh38.p7 | 18:796871 | TTTGAACCAGTGTGA[-/TTTTG]AAATAGATTTAATAA | 7525 |
rs371949378 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776656 | AAAAAGCATTAATAT[A/T]TTTTACATGAATGAA | 7525 |
rs371999406 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:742203 | TTCCTCTAAGTACCA[C/T]CTGCACAGGGAAAAA | 7525 |
rs372002514 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:762110 | CGGATCACCTGAGAT[A/T]GGGAGTTTGAGACCA | 7525 |
rs372020371 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:768183 | GGCAATGTTAAAAAA[-/A]CCATTTCCAAAAGCA | 7525 |
rs372059648 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:731695 | TTTTGAGGCCAGGCA[C/T]GGTGGCTCACGCCTG | 7525 |
rs372059847 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:772496 | AGAGTGCAATGGTGC[G/T]ATCTCGGCTCACTGC | 7525 |
rs372068018 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:792215 | AGGCTGAGGCAGGAG[A/C]ATTGTTTCAACCCAG | 7525 |
rs372070407 | in-del | -/TA | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:814172 | TGATTTCTTTTTTAG[-/TA]TATTCATCAATGTCA | 7525 |
rs372104845 | in-del | -/CTGA | 0.00835141 | 0.0640778 | intron-variant | YES1 | GRCh38.p7 | 18:773768 | CAATCTGATCCAATG[-/CTGA]CTAATAAAAGAAAAA | 7525 |
rs372116654 | snp | C/T | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723935 | TACTGACTGTTTAAC[C/T]TAGAAAAAACTTTTG | 7525 |
rs372117189 | in-del | -/ATGATTTAACA | | | intron-variant | YES1 | GRCh38.p7 | 18:778467 | ACTAAAAATTTTCAA[-/ATGATTTAACA]CATTTCTGAACCTCT | 7525 |
rs372129987 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:782840 | CCTGGGATTACTGGT[A/G]TGCACCACCATGCCC | 7525 |
rs372131608 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | YES1 | GRCh38.p7 | 18:764825 | GTAACCTCCGCCTCC[C/T]GGGTTCATGCGATTC | 7525 |
rs372157622 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:793290 | GTGATCCACCCACCT[C/T]GGCCTCCCAAAGTGC | 7525 |
rs372166794 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:810760 | ATGTCAATTGTGGCA[A/G]GGGTCTCACACTTAT | 7525 |
rs372189095 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:773365 | CAAGAGAAGGCAGAG[G/T]GGAACCAAAAGGGCT | 7525 |
rs372200608 | snp | C/T | | | utr-variant-5-prime | YES1 | GRCh38.p7 | 18:812146 | TCTCATGAGTCGCTG[C/T]TACCGCAGCTCGAGG | 7525 |
rs372227610 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:738948 | CCTGCCTCAGCCTCC[G/T]GAGTAGCTGGGATTA | 7525 |
rs372238764 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:777613 | GAAGTTCAAGACCGG[C/T]CTGGCCAACATGCTG | 7525 |
rs372247497 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:798884 | TTTTAATATAAACCC[A/G]AGATGACATGACTCC | 7525 |
rs372329492 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:743630 | TTTATTTTTAAGGCC[A/G]GGCAAGGTGTCTCAC | 7525 |
rs372333387 | snp | C/T | 3.29473e-05 | 0.00405864 | missense | YES1 | GRCh38.p7 | 18:756587 | GATATGAACTTGGCA[C/T]CACTGAAAATGAGGA | 7525 |
rs372344495 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:751457 | ATGTACTCCCCTCAG[C/T]AACTCTTCATTCTTA | 7525 |
rs372350553 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:769727 | TTTACTAATTGATTA[C/T]TGACTGTTAAGTAAA | 7525 |
rs372354800 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:787634 | AGAATCACTTTAACC[C/T]GGGATGCGGAGGTTG | 7525 |
rs372370674 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:727976 | TTTTGGATTTTTTTG[A/G]ATTTTGGAATATTTG | 7525 |
rs372374459 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:770108 | GGCAGTACAGGCACG[C/T]GCCACCACACCCAGT | 7525 |
rs372439808 | snp | A/G | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:777062 | TTCATTCTTTTGCTC[A/G]AGAAATTATTTCTGA | 7525 |
rs372494733 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:757320 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGCCTC | 7525 |
rs372505188 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:774252 | ACACTGGACTGTTGC[C/T]GAAAAGACTTCTCCA | 7525 |
rs372510491 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:725565 | GGAAGTTTTCTGAGC[C/T]TTTCATCTAACTAGG | 7525 |
rs372522434 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812457 | CCCCAGCCTTCCGGC[A/G]CCTACGCCCCCGTCA | 7525 |
rs372606376 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:770823 | GTGTGGGGGTTGACA[A/G]ATGGTAAACTCCATC | 7525 |
rs372681732 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:808884 | GGTGCTGTGAATCTT[A/C]ATAAACTTTAAACAA | 7525 |
rs372706941 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:799712 | CATTTCAAAAAAAAT[G/T]TTAATTTAAAAATAA | 7525 |
rs372763250 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:745276 | ATAAGAAAAATGCAT[C/T]GTCAGACCAAATTTC | 7525 |
rs372816989 | in-del | -/AA | | | intron-variant | YES1 | GRCh38.p7 | 18:752980 | GGTATGGATGATATG[-/AA]TTATAAAGTATAAAT | 7525 |
rs372882192 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:794949 | GCCTCCCAAGTTGCT[C/T]GAACTACAGGCGCGT | 7525 |
rs372882230 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:807077 | GAATTTGAGACCAGC[C/G]TGGACAACACGGTGA | 7525 |
rs372883470 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:749510 | TCTCAAAAAAACAAA[A/T]GCAAAACAAAAAAAC | 7525 |
rs372886586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:766552 | TACTTCCATAAATAC[A/G]AAAACATAGAAAAGA | 7525 |
rs372888278 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:738159 | ATGTATAGTTTCTCA[A/G]TATAAAGCTTTTCTG | 7525 |
rs372892392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:784634 | AGTTCTTGCCCTTTC[C/T]AGCTTGTGGGGGCTG | 7525 |
rs372903982 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:796298 | AAGCCTATTTCTTTA[A/T]CTGTAAAAATAAAGA | 7525 |
rs372906108 | snp | C/T | 3.44822e-05 | 0.00415209 | missense | YES1 | GRCh38.p7 | 18:745992 | AAAATACCTCGTTGA[C/T]TTCCAGGATTCAAAA | 7525 |
rs372938876 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812724 | ATTCTGCCCCTCTGC[C/T]TTTCTCTGTTCCTTG | 7525 |
rs372952890 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:807846 | CTATATGCCAGCAAT[G/T]CTACTCCCCTCCCCT | 7525 |
rs372956183 | in-del | -/TTAAT | 0.00318978 | 0.0398085 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722498 | GGCCTAATATAAGGC[-/TTAAT]TTAAAGTGTGACTAT | 7525 |
rs373049030 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:731844 | TGGTGGCGGGTGCCT[A/G]TAGTCCTAGCTACTC | 7525 |
rs373122756 | snp | C/T | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722897 | GGAGATCGAGACTAT[C/T]CTGGCTAACACGGTG | 7525 |
rs373124143 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:811366 | AAAAACTAAAGTCCC[G/T]ACACCAGACTTGATT | 7525 |
rs373126797 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:771154 | CAGATCACTTGAGGT[A/C/G]TCAGGAGTTCAAGAC | 7525 |
rs373162455 | in-del | -/A | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723664 | TATTGCCTTAAAAAA[-/A]TCAATGCAACCTCAT | 7525 |
rs373167378 | snp | A/C | 0.000153988 | 0.00877328 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724415 | TGCATATAAAATAGG[A/C]TACTTGAATTATAAA | 7525 |
rs373368928 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:725299 | CTCACCTCACGTCCT[A/G]TCTCCCGCATCACCT | 7525 |
rs373374353 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:735161 | GACTGTGTCTCAAAG[A/C]AAAAAAAAAAAAATC | 7525 |
rs373425458 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:741631 | AAACAGGGTGAAATC[C/T]CATCTGTAGAAAAAT | 7525 |
rs373478419 | snp | G/T | 3.53457e-05 | 0.00420376 | intron-variant | YES1 | GRCh38.p7 | 18:736964 | TACCATCAGCAATCT[G/T]GGAAAGAGAAAAACA | 7525 |
rs373491730 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:789911 | TTAAATACAAAAAAT[C/T]AGCTAGGCATGGTGG | 7525 |
rs373500163 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:757229 | AAAAGTATCGCTGGG[C/T]GCAGTGGCTCACGCC | 7525 |
rs373556410 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:750588 | CCAGGTTGAGAACCA[C/T]TGGTCTAAAAGAATA | 7525 |
rs373561285 | snp | C/T | 1.65949e-05 | 0.00288048 | missense | YES1 | GRCh38.p7 | 18:751804 | AATATAGTAACACCA[C/T]CTATCAGAGGGAAAA | 7525 |
rs373618579 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:761474 | ATACCATGTCAATTC[A/G]CAACAGAGGCTCCTA | 7525 |
rs373648229 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | YES1 | GRCh38.p7 | 18:745757 | AAATTGTGCTCTGGT[C/T]GTGATATAGTATCCA | 7525 |
rs373762915 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:729916 | AGGCGTGAGCCACAG[C/T]GCCCAGCCAGATTTT | 7525 |
rs373779801 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:763141 | AAAATTTCTCTGTTC[C/G]AAGAGTGTGAGGGGC | 7525 |
rs373784871 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:760288 | CAGCCTGGCCAACAT[A/G]GTGAAACCCTGCCTC | 7525 |
rs373788961 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:802524 | ACCCCAGCCTGGGCA[A/G]CAAGAGTGAAACTCC | 7525 |
rs373827705 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:782669 | TCAATATAAAACATG[C/T]AAAAAGGATTATTTT | 7525 |
rs373843588 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:747224 | CCTGTGATCCTAGCA[C/T]TTTGGAAGGCTGAGG | 7525 |
rs373903318 | in-del | -/GTTTT | | | intron-variant | YES1 | GRCh38.p7 | 18:794832 | GTTTTGTTTTGTTTT[-/GTTTT]TTGAGACGGAGTCTC | 7525 |
rs373908303 | in-del | -/C | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:768307 | ATTTTAGAATCTCCA[-/C]AAAAATGCCTGCTGG | 7525 |
rs373908907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:749837 | TGCACTCCAGCCTGG[C/T]GACAGAGCAAGACTC | 7525 |
rs373931083 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:752635 | ACTTAAAGATAAAAA[A/T]GTCATGTTTTGTCTT | 7525 |
rs374034118 | snp | A/G | 0.00517822 | 0.0506191 | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721222 | AATACTTGTAAAAAT[A/G]ATGTCACTCACTTGA | 7525 |
rs374035894 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:740637 | TGCATGGGACAATGA[A/G]TTTGGACAGATTATA | 7525 |
rs374048976 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:731946 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCC | 7525 |
rs374146935 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:782193 | TGCTACTATGCTCAT[A/G]TGCTTCATTCTTCTC | 7525 |
rs374163689 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:792993 | CATCACAGCTTAATG[A/G]CAAACAATAGAAAGA | 7525 |
rs374164158 | in-del | -/TCTC/TCTCTCTC | 0.105924 | 0.204309 | intron-variant | YES1 | GRCh38.p7 | 18:792527 | CACACTGAGACTCCA[-/TCTC/TCTCTCTC]TCTCTCTCTCTCTCT | 7525 |
rs374175295 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | YES1 | GRCh38.p7 | 18:739692 | ATTCCACATTTTAAT[C/T]TACACTTTTAATTCA | 7525 |
rs374204484 | snp | C/G | 3.29457e-05 | 0.00405854 | missense | YES1 | GRCh38.p7 | 18:756674 | GACTGCTGAAATTAA[C/G]TGCTGTTCCCTTTGC | 7525 |
rs374244076 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:771860 | AAAAAGTATTTCCTT[A/G]TGTATCTGCTTGGTA | 7525 |
rs374280156 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:730834 | ATACATTTAAAGTGA[C/T]ACTATGTTGCATGGC | 7525 |
rs374303694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:808568 | AGGTGACCTAAGCCA[C/T]GTAGGGTTCTAAACA | 7525 |
rs374316300 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:766797 | TTGGGCTGTCTTCTT[C/T]CTGTTATGTTCTGGA | 7525 |
rs374329726 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:804913 | AGTGAGACTCTGACT[A/C]AAAAAAAAAAAACAC | 7525 |
rs374360898 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:732311 | TGGGTGTGGTGGTGG[A/G]TGCCTGTAATCCCAG | 7525 |
rs374394553 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:760052 | ACTCATCCTTTTTTA[C/T]GGCTGCATAGTATTC | 7525 |
rs374449758 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:744593 | TAGGGTTTTGCCATG[C/T]TGCCCAGGCTGGTCT | 7525 |
rs374510164 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:743774 | AGCCGGGCATGGTGG[C/T]GCATGCCTGTAGTCT | 7525 |
rs374515886 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:762268 | GAGGCTGCGGTGAGC[C/T]GAGATTGCGTCATTG | 7525 |
rs374523184 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:781033 | CAGCACTTTGGGGCC[C/T]GAGGTGGGTGGATCA | 7525 |
rs374527622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:801908 | AAACACCTTATTTTA[C/T]AAAAAGATGAGGAAT | 7525 |
rs374537561 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:802173 | AGGATTACTTGTGCC[A/G]AGGAGTTCGAGGCTG | 7525 |
rs374537803 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:781455 | CTTAAACGTTCAAGG[A/T]ATCTTCCTTGATCTC | 7525 |
rs374547232 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:764037 | AGGCAGGAGAATGGC[A/G]TGAACCCGGGAGGCG | 7525 |
rs374568780 | in-del | -/CT | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:769381 | GTGTACAAATAAACA[-/CT]GTCTTGCTCTTTACT | 7525 |
rs374581633 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:764044 | AGAATGGCATGAACC[C/T]GGGAGGCGGAGCTTG | 7525 |
rs374585307 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:782893 | AGAGACAGGGTTTCG[A/C]CATATTAGCCACTCC | 7525 |
rs374613149 | snp | A/G | 6.61715e-05 | 0.00575164 | missense | YES1 | GRCh38.p7 | 18:751705 | ATTCATGACACTTAC[A/G]TATTGTTAATTATTT | 7525 |
rs374635951 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:791442 | TCCTTACAACCACCC[G/T]TTCAGTTAAGGACTA | 7525 |
rs374650269 | snp | A/T | 4.94189e-05 | 0.00497062 | missense | YES1 | GRCh38.p7 | 18:747989 | TTCTTTCCTGTAGCG[A/T]TTGATCTTGCTTCCC | 7525 |
rs374656248 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:742070 | GACACACCACTGGAG[A/G]GGGTGACATAATTAG | 7525 |
rs374657147 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:760340 | CCACGTGTGGTGGTG[C/G]GCACCTGTAGTCCCC | 7525 |
rs374658628 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:771592 | TTCACTTTGTCACAC[A/C]GGCTGGAGTGCAGTG | 7525 |
rs374659284 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:734528 | GCCACTGCACTCCAG[C/T]CTGGGTGACAGAGTG | 7525 |
rs374663980 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:778103 | TATGTTACCAGGACA[A/G]GTAGGCATAATCTCT | 7525 |
rs374667982 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:799093 | CAGTTTGCTTTATAC[C/T]AATACTGTAACCCGA | 7525 |
rs374671937 | snp | G/T | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775754 | GTGAGCCGTGATTGT[G/T]CCACTGCACTCCAGC | 7525 |
rs374692424 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:763507 | TGAGAGCAGCCTGGG[C/T]GTCATGGCAGAACCC | 7525 |
rs374764966 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:726575 | ACCTGAGGTCAGGAG[C/T]TTGAGACCAGCCTGG | 7525 |
rs374777072 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:728190 | AAATTAGCTAGGTGG[A/T]TGGCACACACCTGTG | 7525 |
rs374778182 | snp | A/G | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812571 | GGCGGGGTCCGGGGC[A/G]GATTCCCGGGGGCGG | 7525 |
rs374796604 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:760911 | TGTGGAATCTGGTTG[A/G]CACTCTTAATACAGA | 7525 |
rs374807541 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:811217 | GACATAAAATTGTGC[A/T]TCCACCAAAGACTTT | 7525 |
rs374813646 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:752786 | TGTCTGTACTAAAAA[C/T]ACAAAAATTAGCCAG | 7525 |
rs374823505 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:805671 | CTTTCCTTATAACAC[C/T]ATATTGCCTTCTCTG | 7525 |
rs374841402 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:759762 | GTACATGTGCACAAC[C/G]TGCAGGTTACATATG | 7525 |
rs374845820 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:739203 | GCTGGTTCTAATACT[C/T]GTTCTGTTACTAACA | 7525 |
rs374930395 | in-del | -/AT | | | intron-variant | YES1 | GRCh38.p7 | 18:745599 | ATTTATTGGGCATGT[-/AT]TATGTGTAAATAAGT | 7525 |
rs374973870 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:735439 | TTAAAAGTGGGGCTA[A/C]GCTATGAGGACACAA | 7525 |
rs375013403 | in-del | -/GGAGGT | | | intron-variant | YES1 | GRCh38.p7 | 18:801078 | TTGAACCAAGGAGGT[-/GGAGGT]TGCAGTGAGCTGAGA | 7525 |
rs375041374 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:738309 | AACAGTTTTCACTAT[A/G]TATTTAAAACAAAAA | 7525 |
rs375077929 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:764628 | GTTTTAGGTTCATGC[A/T]GTGAAGTCTGGTGGG | 7525 |
rs375193463 | snp | C/G | 1.65767e-05 | 0.00287891 | intron-variant | YES1 | GRCh38.p7 | 18:751696 | TCACAAAATATTCAT[C/G]ACACTTACGTATTGT | 7525 |
rs375237296 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | YES1 | GRCh38.p7 | 18:756512 | TATATATTACCCAAG[A/G]TGATGTTCTCAAACA | 7525 |
rs375263371 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:799830 | CACTTGAACCCAGGA[A/G]GCAGAGATCATGCCA | 7525 |
rs375264645 | snp | A/G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:762671 | AACGTACACTACTCC[A/G/T]GTGACGGGTGCACCA | 7525 |
rs375279994 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:763678 | CACTGCACTCCATCC[C/T]GGATGACAGAGGAGA | 7525 |
rs375302786 | snp | A/G | | | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721427 | CCTGTAGTCCCAGCT[A/G]CTCGGGTGGCCGAGG | 7525 |
rs375329243 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:749730 | CCAGACGTGGTGGCG[A/G]GCGCCTGTAGTCCCA | 7525 |
rs375415998 | snp | A/G | 0.000153988 | 0.00877328 | missense | YES1 | GRCh38.p7 | 18:743322 | CGCAAAGATTCTCGA[A/G]GGATTTCCCAAGCAT | 7525 |
rs375437397 | snp | C/T | 1.64906e-05 | 0.00287142 | missense | YES1 | GRCh38.p7 | 18:745789 | CATTGTCAAGTTTCC[C/T]AATTTTGTAGTGTTT | 7525 |
rs375452426 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:740342 | ATAATCAAGAGAAAA[C/T]ATCACACAAAACCAA | 7525 |
rs375491643 | in-del | -/CA | | | intron-variant | YES1 | GRCh38.p7 | 18:785625 | TAATCCACAATGCAA[-/CA]GTGTTGAGAGGTGGG | 7525 |
rs375554246 | in-del | -/T | 0.00835141 | 0.0640778 | intron-variant | YES1 | GRCh38.p7 | 18:806947 | AGGAATATCTCCAGA[-/T]TTTTCAGTAGATAGT | 7525 |
rs375560602 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:809644 | GCTGGTATATGACAA[G/T]TATGATTTAATAAAT | 7525 |
rs375578373 | snp | C/G/T | 1.64768e-05 | 0.00287021 | synonymous-codon | YES1 | GRCh38.p7 | 18:756576 | TAAACCAGCAGGATA[C/G/T]GAACTTGGCACCACT | 7525 |
rs375587978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:791107 | ATACAAAAATTAGCC[A/G]GGCGTGGTGGTGCGC | 7525 |
rs375615658 | snp | C/T | 0.000132523 | 0.00813903 | intron-variant | YES1 | GRCh38.p7 | 18:724637 | GTTCACCATACCTAA[C/T]ACACAAGATTAAAAC | 7525 |
rs375635277 | in-del | -/AAAAAA/AAAAAAA/AAAAAAAAAAA/AAAAAAAAAAAA/AAAAAAAAAAAAA | 0.0479149 | 0.147179 | intron-variant | YES1 | GRCh38.p7 | 18:804913 | GTGAGACTCTGACTC[lengthTooLong]AAAAAAAAAAAACAC | 7525 |
rs375637353 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:735909 | GGCATGGTGTCTCAC[A/G]CCTGCCATTTTAGCA | 7525 |
rs375791817 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:774067 | CAAACTCCTGACCTT[A/G]TGATCCACCCGCCTT | 7525 |
rs375843651 | snp | C/T | 0.000155988 | 0.00883003 | intron-variant | YES1 | GRCh38.p7 | 18:746077 | ATTAAGTGTTTTGAA[C/T]TGAAAAGTATGAGGT | 7525 |
rs375926543 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:741777 | CTCCACCCTGGGGGA[C/T]AGAGTGAGGCCCCAC | 7525 |
rs375936062 | in-del | -/GAT | | | intron-variant | YES1 | GRCh38.p7 | 18:778338 | AAATGTAACAAACAT[-/GAT]AACATTATTTACAGC | 7525 |
rs375957267 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | YES1 | GRCh38.p7 | 18:746346 | GCAAAATAACAGACC[C/T]TTTCTGTCAGTGACA | 7525 |
rs375966690 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:783151 | GCTACTCAGGAGGCC[A/G]AGGCAGAGGATCACT | 7525 |
rs376052979 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:754712 | AGAGACTCCAACTCC[-/A]AAAAAAAAAAAAAAA | 7525 |
rs376134911 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:767733 | TTGAGTCAGAGTCTC[A/G]CTCTGTGCCTAGGCT | 7525 |
rs376138854 | snp | A/G | | | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721330 | ATCACGAGGTCAGGA[A/G]ATCGAGACCATCCTG | 7525 |
rs376152211 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:749671 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT | 7525 |
rs376156434 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:766618 | AATTTCTCATTCTAA[C/T]TGGTATGTAGTGATA | 7525 |
rs376163194 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:785117 | GACTATTTTGCTTAT[C/G]TGTGGTGGCGGATAT | 7525 |
rs376315446 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon | YES1 | GRCh38.p7 | 18:724550 | CAGATTCATCAATTC[A/G]TGGAGGGATTCTGGA | 7525 |
rs376333205 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:731884 | AGGCAGGAGAATGGC[A/G]TGAAGCTGGGAGGTG | 7525 |
rs376355783 | snp | A/G | 0.0111196 | 0.0737302 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722889 | CAAGGTCAGGAGATC[A/G]AGACTATCCTGGCTA | 7525 |
rs376388785 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | YES1 | GRCh38.p7 | 18:726310 | GGCATCTGTAGTCCC[A/G]GCTACTTGGGAGGCT | 7525 |
rs376454637 | in-del | -/CC | | | intron-variant | YES1 | GRCh38.p7 | 18:793750 | TAGTTTTGTAATATA[-/CC]AAAAATAGTTATAAA | 7525 |
rs376474227 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | YES1 | GRCh38.p7 | 18:739697 | ACATTTTAATTTACA[A/C]TTTTAATTCAAATGG | 7525 |
rs376478804 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:781741 | TTGATCAAATTACTT[C/T]ATCTTTCCTAAGACT | 7525 |
rs376482776 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:802724 | AATCCCAGTTCTGCC[A/G]GTTGTGTGACCTTAG | 7525 |
rs376585848 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:770258 | GAGCCACTGCGCCCG[A/G]CCCTTTTATCTTTTT | 7525 |
rs376619663 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:733256 | TAAGCCAAAGATACA[G/T]GTTATAATATGTGTA | 7525 |
rs376669018 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | YES1 | GRCh38.p7 | 18:757310 | AGATTGAGACCATCC[C/T]GGCTAACACGGTGAA | 7525 |
rs376671687 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:757451 | GAGCTTGCAGTGAGC[A/C]GAGATCGCGCCACTG | 7525 |
rs376671777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:774641 | TCTGACAACTTCTCT[C/T]CACCTCCCACTGCTA | 7525 |
rs376680336 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:795033 | TTAGCCAGGATGGTC[A/T]CAATCTACTGATCTC | 7525 |
rs376683059 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:765395 | AGTATTTTATAATTT[A/G]ACACTTTTTTTTTTT | 7525 |
rs376745038 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:734965 | GAGTTTGAGACCAGC[A/G]TGGCCAACATGGTGA | 7525 |
rs376750098 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:801597 | CACCTAGAAATAAAT[G/T]ATATAATTAGTAGAA | 7525 |
rs376765363 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:809392 | GCAATCTCTGTCTCC[C/T]GGGTTCAAGCGATTC | 7525 |
rs376807937 | snp | C/T | 4.9498e-05 | 0.00497459 | intron-variant | YES1 | GRCh38.p7 | 18:732985 | AATAATGTTGACCAT[C/T]TTGCTTAATTGTTTT | 7525 |
rs376884071 | snp | A/T | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722398 | GTTTGAATTTGAACA[A/T]ATATGCCATGGCACA | 7525 |
rs376897153 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:733836 | CATGAAGTTTATAAA[C/T]TTATTGCAGAAATAA | 7525 |
rs376912930 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:757242 | GGCGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 7525 |
rs376960673 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722864 | TTGGGAGGCCGAGGC[A/G]GGCAGATCACAAGGT | 7525 |
rs376992899 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:764851 | GATTCTCCTGCCTCA[A/G]CCTCCCGAGTAGCTG | 7525 |
rs376993102 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:784559 | GACGCCGGTGTCCCT[C/G]GACTAAAATCAAGGT | 7525 |
rs377045484 | snp | A/C | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724329 | ATTAAAAACATGCAG[A/C]GTAAAGAAGATTTTC | 7525 |
rs377061735 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:767564 | AAAAGCAATTAACCA[C/T]GTATGTGTGTAGGTC | 7525 |
rs377090901 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:792579 | TATGTGTGTGTGTGT[A/G]TGTGTGTATATACAT | 7525 |
rs377093673 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:749193 | AAACAAAACAAAAAC[A/C]CAAAAAAACTGCATT | 7525 |
rs377139130 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:787080 | TGTGATACATACTGT[C/T]TTTTTTTTTTTTTTT | 7525 |
rs377157573 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:763173 | GTTTGTGAGCTGGGT[A/C]GGACAGGCAGCTAGA | 7525 |
rs377164774 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:802758 | ATTATATATACTTTC[C/T]GATTCTCAGTTTCTT | 7525 |
rs377206011 | snp | A/G | 4.94319e-05 | 0.00497127 | intron-variant | YES1 | GRCh38.p7 | 18:748050 | AGCAATCACCGCAAG[A/G]TAGACTATTGCCCAA | 7525 |
rs377278308 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | YES1 | GRCh38.p7 | 18:738167 | TTTCTCAGTATAAAG[C/G]TTTTCTGAATTGTCA | 7525 |
rs377286629 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:775048 | TGCAAAGTCTGAGTC[C/T]GTCACTTACTAGCTG | 7525 |
rs377351610 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:781218 | AGGTTGCAGTGAGCC[A/G]AGATCGCGCCATTGC | 7525 |
rs377355700 | snp | A/G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:802183 | GTGCCGAGGAGTTCG[A/G/T]GGCTGTAATGAGCTA | 7525 |
rs377411245 | snp | A/T | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775840 | TATATAATGCATTAT[A/T]TTGTATTTGACCTCT | 7525 |
rs377415667 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:738064 | TTTTTTTTTAAAAAA[A/C]AAAAATGGATTGCCA | 7525 |
rs377417798 | snp | A/G | 0.0126979 | 0.078662 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722909 | TATCCTGGCTAACAC[A/G]GTGAAACTGCGTCTC | 7525 |
rs377461319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:731801 | TGAAACCCCGTCTCT[A/G]CTAAAAATACAAAAA | 7525 |
rs377467123 | in-del | -/AC | 0.471164 | 0.116561 | intron-variant | YES1 | GRCh38.p7 | 18:786496 | CATTAATAAGTCCAT[-/AC]ACACACACACACACA | 7525 |
rs377472218 | in-del | -/AG | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:765141 | ATACAAGCATAAGAC[-/AG]GGAGAGAAATTAGGA | 7525 |
rs377483043 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:796630 | AAATTAGCCGGGCGT[A/G]GTGGCAGGCATCTGT | 7525 |
rs377488075 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:811868 | CCTCAGGTCGGACTT[A/G]GGCGGGACCCGGCAG | 7525 |
rs377532925 | snp | C/T | 3.32094e-05 | 0.00407475 | missense | YES1 | GRCh38.p7 | 18:743044 | AAGCTTCTGGCATCA[C/T]TGTACCTGGTTTTAG | 7525 |
rs377546453 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:731739 | CTGGGAGGCCGAGGC[A/G]GGCAGATCACAAGGT | 7525 |
rs377606734 | in-del | -/GAG | | | intron-variant | YES1 | GRCh38.p7 | 18:731253 | GACAAGATTACACAG[-/GAG]AAGAGTTCAAGCTAC | 7525 |
rs377621960 | in-del | -/G | | | intron-variant | YES1 | GRCh38.p7 | 18:727948 | AAATGTTTGGGACCA[-/G]AAGTGTTTCCGATTT | 7525 |
rs377650974 | in-del | -/CCCA | | | intron-variant | YES1 | GRCh38.p7 | 18:811714 | ATACACAGACCCCCA[-/CCCA]GCCTTTAGGACCCAA | 7525 |
rs377709565 | snp | C/G | 3.295e-05 | 0.00405881 | intron-variant | YES1 | GRCh38.p7 | 18:748027 | TCCTTCCCTGCAACA[C/G]ATAAAACAGCAATCA | 7525 |
rs377717384 | snp | C/T | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775702 | CTTGGGAGGCTGAGG[C/T]TGGAGGATCGCTTGA | 7525 |
rs386386825 | in-del | -/TT | | | intron-variant | YES1 | GRCh38.p7 | 18:748361 | TCAGTATTCTTTTCT[-/TT]TTTTTTTTTTTTTAA | 7525 |
rs386386826 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:748367 | TTCTTTTCTTTTTTT[-/T]TTTTTTTAAAGCTTT | 7525 |
rs386386827 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:748368 | TCTTTTCTTTTTTTT[-/T]TTTTTTAAAGCTTTA | 7525 |
rs386386828 | in-del | -/TT | | | intron-variant | YES1 | GRCh38.p7 | 18:759704 | AGACAATTTATTTAT[-/TT]TTCTTTTTTTCTTTT | 7525 |
rs386386829 | in-del | -/TT | | | intron-variant | YES1 | GRCh38.p7 | 18:759705 | GACAATTTATTTATT[-/TT]TCTTTTTTTCTTTTA | 7525 |
rs386800142 | multinucleotide-polymorphism | CC/TG | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722917 | CTAACACGGTGAAAC[CC/TG]CGTCTCTACTAAAAA | 7525 |
rs386800143 | multinucleotide-polymorphism | CCT/TGC | | | cds-indel | YES1 | GRCh38.p7 | 18:722917 | CTAACACGGTGAAAC[CCT/TGC]GTCTCTACTAAAAAT | 7525 |
rs386800144 | multinucleotide-polymorphism | AT/GC | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723069 | TGCACTCCAGCCTGG[AT/GC]GACAGAGCGAGACTC | 7525 |
rs386800145 | in-del | ATCA/GGGCAAGGTAACT | | | intron-variant | YES1 | GRCh38.p7 | 18:730958 | TCAGAGAAGGGTGAA[ATCA/GGGCAAGGTAACT]GCAAAGGAGTGATTA | 7525 |
rs386800146 | multinucleotide-polymorphism | CA/TG | | | intron-variant | YES1 | GRCh38.p7 | 18:731693 | AATTTTGAGGCCAGG[CA/TG]CGGTGGCTCACGCCT | 7525 |
rs386800147 | in-del | A/CAAACATTACAGATAGGAAGG | | | intron-variant | YES1 | GRCh38.p7 | 18:736191 | AAACAACAACAACAA[A/CAAACATTACAGATAGGAAGG]CATTCCAGATGGAGG | 7525 |
rs386800148 | multinucleotide-polymorphism | AG/GA | | | intron-variant | YES1 | GRCh38.p7 | 18:807819 | CCTAGGAGAAAGTAG[AG/GA]TCCAAAGAACCTATA | 7525 |
rs386800149 | multinucleotide-polymorphism | ATTAAAGAT/GTTAAAGAG | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813621 | AAGGTAGGCGTAGGC[ATTAAAGAT/GTTAAAGAG]ACACATAATGTGGAA | 7525 |
rs397694456 | in-del | -/T | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813661 | ATGCTGTATTTTCTT[-/T]AGCTACTAAAACTTC | 7525 |
rs397723072 | in-del | -/T | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:744407 | TCTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCAC | 7525 |
rs397728408 | in-del | -/A | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:749875 | AAAAAAAAAAAAAAA[-/A]GTTATCTAGAAATAT | 7525 |
rs397732104 | in-del | -/A | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:751892 | GCCAAAAAAAAAAAA[-/A]GCTTAAGGATAGTTT | 7525 |
rs397741992 | in-del | -/T | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:791084 | TGAAACCCCATCTCT[-/T]ATTAAAAATACAAAA | 7525 |
rs397744513 | in-del | -/A | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:754730 | AAAAAAAAAAAAAAA[-/A]TCTCAGCTCAAATGA | 7525 |
rs397762724 | in-del | -/TT | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:759706 | ACAATTTATTTATTT[-/TT]CTTTTTTTCTTTTAT | 7525 |
rs397766475 | in-del | -/A | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:748808 | TAGATAAAAAAAAAA[-/A]TCACAATGCTCTAAC | 7525 |
rs397771030 | in-del | -/TT | | | intron-variant | YES1 | GRCh38.p7 | 18:769970 | TCTTTTTTTTTTTTT[-/TT]GAGACGGAGTCTTGC | 7525 |
rs397774549 | in-del | -/A | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:807349 | AAAAAAAAAAAAAAA[-/A]TTAGCCAGGCATGGT | 7525 |
rs397786794 | in-del | -/G | | | intron-variant | YES1 | GRCh38.p7 | 18:736342 | GGGGGGAAGGGGGGG[-/G]TTTGCCTGCACATTT | 7525 |
rs397796350 | in-del | -/A | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:728335 | TCAAAAAAAAAAAAA[-/A]TTCATTTATGTTTCA | 7525 |
rs397812896 | in-del | -/T | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:739926 | GCTTTTCATTTTTTT[-/T]AAATTTTGTGCAGTT | 7525 |
rs397830708 | in-del | -/T | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813660 | GATGCTGTATTTTCT[-/T]TAGCTACTAAAACTT | 7525 |
rs397858164 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:773849 | TTCCCTTTTTTTTTT[-/T]GAGACGGAATCTTGC | 7525 |
rs397858464 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:785791 | GGAAAAAAAAAAAAA[-/A]AGCCAGGCGCTGTTG | 7525 |
rs397858676 | in-del | -/T | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776211 | TCTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCCC | 7525 |
rs397858824 | in-del | -/AC | | | intron-variant | YES1 | GRCh38.p7 | 18:783411 | CACACACACACACAC[-/AC]GGAAAAAATAATCAC | 7525 |
rs397858908 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:770285 | TTTTTTTTTTTTTTT[-/T]AAGAGTTTTTAAGAT | 7525 |
rs397859075 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:769041 | CTTACCATTGTGTTA[-/A]CAACTGCCTACAGCA | 7525 |
rs397944203 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:749875 | AAAAAAAAAAAAAAA[-/A]GTTATCTAGAAATAT | 7525 |
rs398031821 | in-del | -/T | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:785166 | ACCTTTTTTTTTTTT[-/T]AACCTCATCAGCTAT | 7525 |
rs398031822 | in-del | -/G | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:792868 | AAAGCCAAGGGGGGG[-/G]AAAAAGCTTAAATCA | 7525 |
rs398031823 | in-del | -/T | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:810024 | TTTTTTTTTTTTTTT[-/T]AATTACCCAAGTTTG | 7525 |
rs398058972 | in-del | -/AA | | | intron-variant | YES1 | GRCh38.p7 | 18:751891 | CAGCCAAAAAAAAAA[-/AA]GCTTAAGGATAGTTT | 7525 |
rs398120089 | in-del | -/A | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723111 | AGAAAACAAAAAAAA[-/A]GTGAATGTAGATTCA | 7525 |
rs527275747 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:790204 | AACATGGTGAAATCC[C/T]GTCTCTACTAAAAAT | 7525 |
rs527283157 | snp | C/T | | | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721095 | CCCCTTAATTTATAA[C/T]AAAACTGGTCATTCT | 7525 |
rs527298812 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:782406 | AAGAGGCAGGGTCAC[G/T]GATGGAACATGGCAG | 7525 |
rs527381395 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:757755 | TGAACCCAGGAGGAA[G/T]AGGTTGCAGTAAGCT | 7525 |
rs527387814 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:753473 | CATAATCCCACTGAC[G/T]TGTCAGATCAAAAAA | 7525 |
rs527390066 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:752850 | TGGGAGGTTGAGACA[G/T]GAGAATCGCTTGAAA | 7525 |
rs527408931 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:796669 | TTGCTGAGGCAGGAG[A/G]ATCACTTGAACCCGG | 7525 |
rs527524135 | snp | C/G | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813244 | ATACACGCACCTTTC[C/G]TATGAGCCTTGTAAA | 7525 |
rs527530038 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:770023 | CAGTGGCGTGATCCC[A/G]GCTCACTGCAACTGC | 7525 |
rs527554846 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:783100 | TTTAAAAATTATATA[G/T]CCACTAGGTTTGGTG | 7525 |
rs527571793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:747208 | GGCACAATGGCTCAC[A/G]CCTGTGATCCTAGCA | 7525 |
rs527577276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:740304 | AAGTCTGATTACGGC[C/T]TCACTATTATTTGTT | 7525 |
rs527615144 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:734719 | GATGTTGGTGTGGAT[A/G]TGGTGAAAAGGGAAC | 7525 |
rs527616943 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:740956 | AGGCTGGAGTGCAGC[A/G]GTGTCATCTTGGCTC | 7525 |
rs527623986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:740894 | CAATATCTTTTTTAA[C/T]TGTTAAAGTCTTTAT | 7525 |
rs527632689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:804236 | AAGTTTTTATTCAAA[C/T]AGCCACGATTACTTG | 7525 |
rs527704359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:798245 | TGTTCTGTGTCACCT[A/G]TTATTTCAAGTTTCC | 7525 |
rs527717575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:759205 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAACA | 7525 |
rs527746584 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:770855 | TGGTCACTTGAAAAT[G/T]CTGAAAAGTTGCCAG | 7525 |
rs527807220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:758621 | CATCACAAATGTTAC[C/T]TTTCCATTCAGGCTT | 7525 |
rs527822107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:803740 | AGGGTGACTGGCAAG[A/G]CTACAGGTTCACCCA | 7525 |
rs527828610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:730747 | ATTTAACTTTTGTAG[C/T]TGTTTACAGTGCTAT | 7525 |
rs527831486 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723355 | CATGACATCAACATT[A/G]AACATTACCTTCCAT | 7525 |
rs527851173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:748497 | TTTTAGAATATTTTC[A/G]TCACCCCCAAAAGAA | 7525 |
rs527885552 | snp | C/T | 0.0126979 | 0.078662 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722863 | TTTGGGAGGCCGAGG[C/T]GGGCAGATCACAAGG | 7525 |
rs527890601 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:772244 | ATGTTGGTCAGGCTG[G/T]TCTCAAACTCCCAAC | 7525 |
rs527951347 | in-del | -/AG | 0.00398564 | 0.0444627 | intron-variant | YES1 | GRCh38.p7 | 18:801719 | TGTATGTGTATATAC[-/AG]AGAGAGAGAGAGAAT | 7525 |
rs527986830 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:754709 | AGAGAGAGACTCCAA[C/T]TCCAAAAAAAAAAAA | 7525 |
rs528000744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:755241 | TGTATGGCAGTCCTC[C/T]GGCCATTGCCTTTTT | 7525 |
rs528007865 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:798776 | GGGGGTACACTGTCC[A/G]TTAGAATTTTAAGCC | 7525 |
rs528018709 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:791997 | CTCAATTTGGACTAG[A/C]CACATTTCAAGTGCT | 7525 |
rs528029856 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:807121 | CAAAAAATTCAAAAA[G/T]TAGCCAGGCATGCTC | 7525 |
rs528044236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:800358 | GATCCCTACCCTCAC[A/G]GAGCTTACATTCCAG | 7525 |
rs528058385 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:721921 | TAAGACACTGAAGAC[A/G]AAAAGCTGTTGGAAA | 7525 |
rs528069027 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | YES1 | GRCh38.p7 | 18:729359 | GGCGGAGGCTGCAGT[A/G]AACCAAGATCGTGCC | 7525 |
rs528089325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:800886 | GGTGTGGTGGCTCAC[A/G]ACTGTAATCCCAGCA | 7525 |
rs528135114 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:766427 | AATGTAAGTTAAAAC[C/T]GCAAAGGGATAGCAC | 7525 |
rs528154381 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812468 | CGGCGCCTACGCCCC[C/G]GTCAGGTCCCCTCCG | 7525 |
rs528160469 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:749808 | GAGCTTGCAGTGAGC[C/T]GAGATTGCGCCACTG | 7525 |
rs528165536 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:779444 | AAATGTATAGAATAA[-/T]TTTTTTTGTTATAGA | 7525 |
rs528202769 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:741879 | CAGTAGACATTCCTT[C/T]CAAAGAGCGCCAGGT | 7525 |
rs528214830 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:806448 | CGAGCTATGAAAAAG[C/T]ATTAAGCTAGTTTTA | 7525 |
rs528215102 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812956 | GTTCACGTCTTGCCT[C/T]CTTCCGAGGCAGGGA | 7525 |
rs528257099 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:751621 | TACCTCTCTCATCTC[C/T]GGATCATCAACCAGC | 7525 |
rs528273335 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:783445 | AACCTATAGCTCTAA[A/G]GGAATTAATATGAAT | 7525 |
rs528278086 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:795294 | ACATGCCATTTGCAA[C/T]TAACTTTCAAATGGT | 7525 |
rs528292620 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:787350 | GTGGTCCGCCCGCCT[C/T]GGCCTCCCAAAATGC | 7525 |
rs528305088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:780408 | CAACTGGTGGCTTTA[C/T]AAGAGGAAGAGAGAT | 7525 |
rs528332692 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | YES1 | GRCh38.p7 | 18:759183 | CATCAAAATATAACC[A/G]GGGCTAGGCGCGGTG | 7525 |
rs528403136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:794798 | GGGTGTCTGTCTTCA[C/T]ATGTGGGTTTTTGGT | 7525 |
rs528476068 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:734177 | CCAGCTACTCGGGAG[C/G]CTGAGGCAGGAGAAT | 7525 |
rs528485926 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:728420 | TTTCTGCACAAAACA[A/C]AATTTTGATGGTATT | 7525 |
rs528546278 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:810449 | CAGGTCAAAGCTGTA[A/G]TTTCACTTTCAGATG | 7525 |
rs528548521 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:773462 | TGTCTTGTCACCCCC[-/T]AAAAGAAGGTAAATC | 7525 |
rs528559082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:738383 | ATCTTAATTCTTGTG[C/T]TGGACTATAGTAAAT | 7525 |
rs528566145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:745319 | CTTTAGGAAAGCTTA[C/T]GCGATCCAGCCCATG | 7525 |
rs528569498 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:781175 | TCAGGAGGCTGAGGC[A/T]GAAGAATTGCTTGAA | 7525 |
rs528587448 | in-del | -/AAAAAAA | 0.194278 | 0.243711 | intron-variant | YES1 | GRCh38.p7 | 18:777807 | GTGAGACTCTGGCTT[-/AAAAAAA]AAAAAAAAAAAAATT | 7525 |
rs528666059 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:754288 | CTCTGTTTATACTAG[G/T]CTCCACACTAATACT | 7525 |
rs528694738 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:757431 | TGGCGTGAACCCGGG[A/G]GGCGGAGCTTGCAGT | 7525 |
rs528694771 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | YES1 | GRCh38.p7 | 18:763830 | AGAGGAGACATTAAG[A/G]AAAAGTCGAGGCCAG | 7525 |
rs528698337 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722997 | CTCGGGAGGCTGAGG[C/T]AGGAGAATGGTGTGA | 7525 |
rs528717529 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:762887 | TGTACAATGTGAAAA[A/C]TGCTAGAGTGTGACA | 7525 |
rs528738995 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:797366 | AGAAAGAGCTTTAAA[A/C]CTGCTAACATCCCTG | 7525 |
rs528744278 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:768451 | TACAGACTTTTCCCA[A/G]CAGTGTTTTATAGTT | 7525 |
rs528780627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:763491 | CTTGAGCCTAGAAAT[C/T]TGAGAGCAGCCTGGG | 7525 |
rs528824368 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:728929 | TTTGCTTGAATTTCA[A/C]TGAGTTTAATTTTCT | 7525 |
rs528837109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:808427 | ATAATACATACCCTA[C/T]CATAGCCATACACGA | 7525 |
rs528868362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:735758 | ATATTGGGTACAGTG[C/T]AAGATGCTTGGGTGA | 7525 |
rs528893264 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:730865 | TGTGTGGTTTTTTTC[C/T]AGCCCTGTCTGCAAG | 7525 |
rs528922384 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:771003 | GAAGAGATATCCCAT[C/T]TCAAAAAAAAAAAAA | 7525 |
rs528934225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:747699 | AAAGAGAGAGACTAG[A/G]CATAAGGAAATATGA | 7525 |
rs528952404 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:741117 | TGGCCAGGCTGGGAT[C/T]GAACTCCTGACCTCA | 7525 |
rs528960204 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:783892 | GTGCTGGGATTACAG[A/G]TGTGAACCACCGCAC | 7525 |
rs528989968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:741717 | CTGAGATGAGAGGAT[C/T]GCTTGAGCCCAGGGA | 7525 |
rs529049893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:804979 | CTTAATTAGTAGAAC[C/T]GCAATTTGCTTGAGA | 7525 |
rs529087575 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:733383 | TTTTATATCATTCTG[A/G]AAAATTTTATTGTAC | 7525 |
rs529101524 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:799024 | AAATTAAATTAGTCA[C/G]ATGCTCTGCTTTAAG | 7525 |
rs529121959 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:758138 | GGTAAAATTAACTTT[A/G]GTATTTTATTTAACC | 7525 |
rs529178188 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:810642 | AAGGCAATTGTCTTT[G/T]TCAAATGTAGGACCC | 7525 |
rs529238527 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:749529 | AAACAAAAAAACCCC[A/C]TGAATTTCTAGAATA | 7525 |
rs529243583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:811335 | CCGAACTGTTAAGTC[C/T]TACTCATTACAAAAC | 7525 |
rs529253888 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:724821 | TGCTAATCTATGTTT[G/T]AACATGTCTAATTTT | 7525 |
rs529261425 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:785417 | AATACTGAGTGTTAG[C/G/T]GGGGAGAAAGAGAAA | 7525 |
rs529285604 | snp | C/T | | | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721438 | AGCTACTCGGGTGGC[C/T]GAGGCAGGAGAATGG | 7525 |
rs529312795 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:741149 | GTGATCTGCCTGCCT[C/T]GGCCTCCCAAAGCGC | 7525 |
rs529336627 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:738606 | GAGGCGGGAGAATTG[C/T]GTGAACCTGGGAGAT | 7525 |
rs529373952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:792826 | GTAAAAAAGAAAGAA[A/G]AAGAAGAAAAGTTAT | 7525 |
rs529375362 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:756151 | CGCTACTCTACTGTC[A/C]TTTAATTAACATCTA | 7525 |
rs529376826 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:766760 | TTTTAAACTAAAGTG[C/T]CTGTTCAAATCAAAT | 7525 |
rs529380484 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:755393 | AGCTGGGACTACAGG[C/T]GCGCAACACCACACC | 7525 |
rs529394917 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:748687 | TTGGCATAATTTTTT[A/G]AAGGTTCATCTAGGT | 7525 |
rs529447516 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:795862 | ACACCATGGCACATG[C/T]GTACCCATGTAACAA | 7525 |
rs529472623 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:732566 | ACAGTAAGAGGCCCC[G/T]TTGGAAAATGTCCTG | 7525 |
rs529475157 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:772104 | CACGATCTCGGCTCA[C/T]GGCAACCTCTGCCTC | 7525 |
rs529519090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:778533 | TATAAATGAACTCTA[A/G]TAAGTTAACTAATTG | 7525 |
rs529555799 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:792371 | GGGTTAAAAAAATAA[A/C]ATAAAAAATAAAGAA | 7525 |
rs529591262 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:743598 | TGAAATATACATAAG[G/T]GAAACATTTTGTAAA | 7525 |
rs529623326 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:772582 | GGATTACAGGCACAC[A/G]CCACCATGCCCAGCT | 7525 |
rs529640813 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:796064 | TACATTACAAAGATG[C/T]CCATCCTTCCTACAT | 7525 |
rs529647749 | snp | A/T | 1.71041e-05 | 0.00292434 | missense | YES1 | GRCh38.p7 | 18:736949 | TTTCAATATATGCCA[A/T]ACCATCAGCAATCTT | 7525 |
rs529657424 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:752762 | AGCCTGGTCAACAGG[C/G]CGAAACCCTGTCTGT | 7525 |
rs529699266 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:802880 | TTGAGCCCAGGAGTT[C/T]GAGACAGCCTGGGCA | 7525 |
rs529722892 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:735000 | GTGTCTCTACTAAAA[C/T]ACAAAAATTAGCCGG | 7525 |
rs529728871 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:763473 | GCTGAGGTGGAAAGA[C/T]TGCTTGAGCCTAGAA | 7525 |
rs529748629 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:800397 | ATTCCAGTCATTTGG[A/T]GTTGGTACAACAGCA | 7525 |
rs529754493 | snp | A/G | 1.65247e-05 | 0.00287438 | missense | YES1 | GRCh38.p7 | 18:751765 | TCTTCTGTAGTTCTA[A/G]CTTCATAATCATATA | 7525 |
rs529760463 | in-del | -/TC | 0.00557542 | 0.0525036 | intron-variant | YES1 | GRCh38.p7 | 18:743898 | GTGACACAGTGAGAT[-/TC]TGACTCGAAAAAAAA | 7525 |
rs529775772 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:795594 | AAAGAAATGAGTTCA[A/T]GTCCTTTGCAAGGAC | 7525 |
rs529798373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:757411 | GGGAGGCTGAGGCAG[A/G]AGAATGGCGTGAACC | 7525 |
rs529822246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:734214 | AACCTGGGGGGCAGA[A/G]GTTGCAGTGAGCCAA | 7525 |
rs529827145 | snp | C/T | 0.084364 | 0.187256 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722917 | CTAACACGGTGAAAC[C/T]GCGTCTCTACTAAAA | 7525 |
rs529828179 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:774637 | AGTATCTGACAACTT[C/G]TCTCCACCTCCCACT | 7525 |
rs529833434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:802054 | TCTGACCTTAATTAA[C/T]AGCTGATATCTATTA | 7525 |
rs529834876 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:769648 | AATTTTGTCAAAAGC[-/T]TTTTCTACATGTACT | 7525 |
rs529875098 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:782344 | TCCTAAAGGACCCTG[A/G]CCCAGCTTGGATCAG | 7525 |
rs529888103 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:740208 | GGTAGCTAAATGAGT[C/T]GCTGTGGAACTACTG | 7525 |
rs529894305 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:783412 | ACACACACACACACA[C/T]GGAAAAAATAATCAC | 7525 |
rs529903142 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:790168 | ATCACCTGAGGTCAG[A/G]AGTTTGAGATGAGCC | 7525 |
rs529909160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:781894 | ACTTATGGCTTCAAG[A/G]ACAGAATCTGACTAG | 7525 |
rs529909897 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:734626 | ATCATCAGGGAAATG[C/G]AAATTAAAACTACAG | 7525 |
rs529940533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775332 | AAAATAAATGTACAA[A/G]TGAATGAATTACATA | 7525 |
rs529994112 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:746168 | AATAGCTAGAGAACA[C/T]GGCTCAAAATACAGG | 7525 |
rs530168097 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:769243 | GTCTTTAAAGTGACG[A/T]GCGACCGTAAGTAAA | 7525 |
rs530200397 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:754592 | GTTTGTTTCTTGTTA[C/T]CTCAGCTACTCGGGA | 7525 |
rs530221977 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:725850 | GATTGCGCCATAGCA[C/T]TCCAGCCTGGGTGAC | 7525 |
rs530231122 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:769917 | TTGGTATCAGGATGT[G/T]GGCCTCACAAAATGA | 7525 |
rs530261393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:729517 | TTTCATTATTTTGCA[A/G]AACTTTTCTTCTATT | 7525 |
rs530329535 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:783358 | ATCTTGTTCCAAACT[A/G]AACAGAAAACTCTTC | 7525 |
rs530385984 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812431 | GGGCCACGCCGGCCC[A/G]GCTCCGGGGCCCCCA | 7525 |
rs530392098 | in-del | -/TTTC | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:782684 | TAAAAAGGATTATTT[-/TTTC]TTTCTAATTTTAACT | 7525 |
rs530415267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:758571 | TATTCTCCCCACCTC[C/T]CTACCTGCTAAAATC | 7525 |
rs530427142 | in-del | -/GT | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:791956 | GCTACTCGAAATCGG[-/GT]GTGTATTTTACACTT | 7525 |
rs530446364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:806420 | TGAGAGCAAAAATCT[A/G]AAGAATTAACTTCGA | 7525 |
rs530451435 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:797406 | ATCACCAAAAGAAAA[A/G]GCAACACCTATCATG | 7525 |
rs530464794 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:791883 | AACATGGTGAAACCC[C/T]GCCTCTACTAAAAAT | 7525 |
rs530485080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:805997 | TTCAGGGGTCAGTAC[C/T]TTTCCTCCTAGCACT | 7525 |
rs530488842 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:732452 | AAAAAAAAAAAAAAA[A/C]AAAAACAAAACACCA | 7525 |
rs530509859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:736707 | CTATGACTCTTCTGA[A/G]GGAAGCTAAAACAAT | 7525 |
rs530515665 | in-del | -/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:738081 | AAAATGGATTGCCAA[-/C]CTCCCCTACCATAGA | 7525 |
rs530550486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:766244 | CCAGTTGGCTAGTTG[A/G]GCCATGAGCATGGGC | 7525 |
rs530552541 | in-del | -/TT | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:751408 | GAGCATCAAACTCTC[-/TT]TATAAAGTTTTTTAA | 7525 |
rs530554693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:760392 | GAAGAATCGCTTGAA[C/T]CTGGGAGGCGGAGGT | 7525 |
rs530584488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:750089 | AAAACTGAAAAGGCA[C/T]TGTCTAAATTAAAAT | 7525 |
rs530587098 | snp | C/T | | | synonymous-codon | YES1 | GRCh38.p7 | 18:756705 | TGAAGATGACGGACA[C/T]GGTGACACTGTAGTG | 7525 |
rs530641159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:772514 | CTCGGCTCACTGCAA[C/T]CTCCGCCTCCTGGGT | 7525 |
rs530693565 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:770270 | CCGGCCCTTTTATCT[-/T]TTTTTTTTTTTTTTT | 7525 |
rs530724052 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:794027 | TCCCAGAACAACTCT[G/T]ACTGCAATAATTAAT | 7525 |
rs530727915 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:786138 | TATAGCAACACAAAA[C/T]AAACTAAGAAACCCT | 7525 |
rs530750153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:800227 | CTTTCTCTCATGCCC[A/G]TGATAGGCAGAACAT | 7525 |
rs530753498 | snp | G/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:721848 | TATTCATTTAAAAAA[G/T]TGTGCTAGAAGGCTG | 7525 |
rs530758363 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:789360 | GCTGAGGTGGGAGGA[C/T]GGCTTGAGCCCAGGA | 7525 |
rs530786204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:738275 | CAAATACCTACCACA[C/T]ATCTGAAGAGAAACT | 7525 |
rs530790295 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:780210 | GCACTCCAGCTTGGG[C/T]GACAGAATGAGACTT | 7525 |
rs530790969 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:760892 | TATATAATAAATGTA[A/C]ACATGTGGAATCTGG | 7525 |
rs530799828 | snp | A/G | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813466 | TTGGTTTCCTTTGCG[A/G]TTTTTAGTGAAATTC | 7525 |
rs530822137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:733138 | TTTAAAATTCATATT[A/G]AAATAAATCACATTT | 7525 |
rs530848317 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:773320 | TTCCCTCCTCATACC[C/T]GAACTACTTTCATCT | 7525 |
rs530861788 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:786530 | ACACACACACACACA[A/C]ACACACAGAGTTGCT | 7525 |
rs530918962 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:801503 | GGGCAAATTAGAAAA[C/T]GGCTATCTTTCTGCA | 7525 |
rs530952013 | snp | C/T | 0.00010022 | 0.00707815 | missense | YES1 | GRCh38.p7 | 18:745711 | ATATTCACATACCTG[C/T]GTAGTGTTTCACCAA | 7525 |
rs530959322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:807871 | TCCCCTAAACAACAA[C/T]AAAAGAAGCAATTCT | 7525 |
rs531112012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:728348 | AAATTCATTTATGTT[C/T]CATATACACCTTATA | 7525 |
rs531122724 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:767682 | CTTGAAATTATATAA[C/T]ATAAAGCCTCCAGTT | 7525 |
rs531249421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776126 | TCCAGAGTAGCTATA[A/G]CAGTTTATACTCTCA | 7525 |
rs531250887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:783796 | ATTTTTGTATTTTTA[A/G]TAGAAACGGGTTTCA | 7525 |
rs531286483 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:733522 | GGCGCGGTGGCTCAA[C/G]CCTGTAATCCCAGCA | 7525 |
rs531288663 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:741055 | GGCACAAGCCACCAC[A/G]CCCAGCTGTTTTTTG | 7525 |
rs531305870 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:746783 | AGGTGAATTTTTACT[G/T]TTTAAAAGTTGCAAA | 7525 |
rs531305879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:753979 | AAATACTATTTACTT[C/T]CCATTTCCACTGCTG | 7525 |
rs531312227 | in-del | -/TCCCTT | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:802633 | AAAAGACAAGAAATC[-/TCCCTT]TCCATCATTGCTCCT | 7525 |
rs531316443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:747257 | GGTGGATCACTTGAG[A/G]TCAGGAGTTTGAGAC | 7525 |
rs531408247 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:737192 | GTGCGGTGGCCCACA[A/C]CTATAATCCCATTAA | 7525 |
rs531430366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:811143 | AAGATACTATAATCA[C/T]ATCATGTGAAATCGA | 7525 |
rs531495951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:810556 | AGTGGTTACAACAGA[A/G]TATATATTTTAAGAG | 7525 |
rs531517642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:770963 | GCAGTGACAGTAGGT[A/G]CCACCGCACTCTGCT | 7525 |
rs531557228 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:804272 | TGACATCATAACTAT[A/C]CACTTCAACAGAATA | 7525 |
rs531579935 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:729175 | GATACTTTGTTAATG[G/T]GTCTGAATCCACTAA | 7525 |
rs531589789 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:777982 | TGTTGTACAGTGTTA[C/T]ACTGTTAAAGTATTT | 7525 |
rs531595656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:798838 | AGTCTAGTGCACACA[C/T]CTTAAAATCCAGAAC | 7525 |
rs531665714 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:730447 | ATTCCTGGGCTCAAG[C/T]GATCCACCCACCTTA | 7525 |
rs531748654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:804855 | GGAGGCTGAGGTTGT[A/G]GTGAGCTGAGATCAA | 7525 |
rs531784422 | in-del | -/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813576 | ATAAGGGTTTGAACA[-/T]TTTTTTTCTTCAGCT | 7525 |
rs531821981 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:759299 | TGGTGAAACTCCGTC[A/T]CTATTAAAAATACAA | 7525 |
rs531851513 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:778453 | TATTAGTAACAGTGA[C/T]TAAAAATTTTCAAAT | 7525 |
rs531856282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:793283 | AGACCTCGTGATCCA[C/T]CCACCTCGGCCTCCC | 7525 |
rs531879831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:725399 | TATTTAAAATAGTCT[A/G]TGATTCTCTAAAGAA | 7525 |
rs531910191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:777682 | CATGGTGGTGTGCGC[C/T]TGTAATCCCAGCTAC | 7525 |
rs531917119 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:741650 | TGTAGAAAAATACAC[-/A]AAATTATCTATGTGT | 7525 |
rs531987968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:795426 | CTTTGTGCTACTCTT[A/G]CAACTTTTCTGAACT | 7525 |
rs531990153 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:749738 | GGTGGCGGGCGCCTG[C/T]AGTCCCAGCTACTCG | 7525 |
rs532019380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:748655 | TTATGTGGTCTTTTG[C/T]AATTGACTTCTTTTA | 7525 |
rs532048110 | snp | A/G | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775780 | CCAGCCTGGGTGACA[A/G]AGTGAGAACTTGCCT | 7525 |
rs532055230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:749454 | AGTCAGCCAAGATCA[C/T]GCCATTGCACTCCAG | 7525 |
rs532070128 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:762062 | GTGGTGGTGCATGCC[C/T]GTAATCCCAGCACTT | 7525 |
rs532113838 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722833 | CGCGGTGGCTCACGC[C/T]TGTAATCCCAGCACT | 7525 |
rs532149856 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722585 | TTCCTTTGCTAGACA[C/T]TCAAACCACTAATGC | 7525 |
rs532156117 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | YES1 | GRCh38.p7 | 18:757358 | AATGCAAAAAATTAG[A/C]CGGGCGTGGTGGTGG | 7525 |
rs532188666 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | YES1 | GRCh38.p7 | 18:781224 | CAGTGAGCCGAGATC[A/G]CGCCATTGCACTGCA | 7525 |
rs532219831 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:804859 | GCTGAGGTTGTAGTG[A/G]GCTGAGATCAAGCCA | 7525 |
rs532243297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:795969 | ATGAGTAAGTAAAAC[A/G]AAAGTTCAGAGTCTA | 7525 |
rs532250935 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:786602 | GCCAAAATTAATACC[A/G]TATCAGTTCAGGGTG | 7525 |
rs532274739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:788272 | CCTTTCTATTTTCAT[A/G]TTACATGGGGAGCCT | 7525 |
rs532285861 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:728194 | TAGCTAGGTGGATGG[C/G]ACACACCTGTGGTCT | 7525 |
rs532306216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:746145 | TGGGATAGGTTTGGA[C/T]GACAAAGAATAGCTA | 7525 |
rs532315037 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:745355 | GAAGGTAATCCTTCT[C/G]ACATAGCTTTTTCTG | 7525 |
rs532316250 | in-del | -/AAATA | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:752951 | CTGTATCAAAAAAAT[-/AAATA]AAATAAAATGGTATG | 7525 |
rs532333709 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:803253 | AACAAAAAATAAATA[A/C]CCATCTCATTCCTAA | 7525 |
rs532339709 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:734481 | GAATGGCGAGAACCC[A/G]GGAGGCAGAGCTTGC | 7525 |
rs532345979 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:738457 | GCACTTTGGGAGGCC[A/G]AGGCGGGCAGATCAC | 7525 |
rs532376510 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:729425 | GTCCCAAAAGAAAAT[A/C]AATAAATAAATAAAT | 7525 |
rs532397164 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:808239 | CATGTGAAAACGATA[C/T]TGGCGGCAGCACTGG | 7525 |
rs532428797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:763592 | CCTATAGTTCTAGCT[A/G]CTTGGGAGGTTGAGG | 7525 |
rs532459249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:752497 | TTGACAGAAAAAGGA[C/T]TGATGACTACTACAA | 7525 |
rs532497487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:734201 | GGAGAATTGCTTGAA[C/T]CTGGGGGGCAGAGGT | 7525 |
rs532601356 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:790312 | ACCCGAGAGGCGGAA[G/T]TTGCAATGAGCCGAG | 7525 |
rs532604207 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:753535 | TCTGTTGCCCAGGCT[A/G]GAGTGCAGTGGTACG | 7525 |
rs532629976 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:739483 | TGGCCTGTGCCTGCA[C/G]TCCTAGCTACCCAGG | 7525 |
rs532631501 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:726406 | CTCCAGCCTGGGTGA[C/T]AGAGTGGGACTCCAT | 7525 |
rs532670273 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:768658 | TAAGATTATAATACT[C/G]TATTTTTACCATACC | 7525 |
rs532713271 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:792922 | ACTCTCATGAACTAA[A/G]AATAGAGGAATCCTT | 7525 |
rs532750126 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:796748 | GTGACAGAGGAAGAC[C/T]CTGTCTCATAAAATA | 7525 |
rs532762817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:797302 | TTCATATATATAACA[A/G]AAATAAAACAATGTT | 7525 |
rs532803300 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:752811 | AGCCAGGCATGGTGG[C/T]GCATGCCTGTAATCT | 7525 |
rs532869565 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:742548 | TTAAAATGAGAAAAC[G/T]AATTCATTTTAACTT | 7525 |
rs532923732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:771379 | TCTCAAAAAAAAAAA[A/G]AATTCATTTGAGTGC | 7525 |
rs532946333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:725594 | GGTACTGTCATCTTC[A/G]TAAGTGAAATCTGGC | 7525 |
rs532996047 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:756260 | TATATGTTTTTAATC[A/T]TTATGTTCCCGGTGC | 7525 |
rs533011883 | in-del | -/C | 0.00597247 | 0.0543191 | intron-variant | YES1 | GRCh38.p7 | 18:729943 | TTTGAACTCTTGATA[-/C]ATCAGTCATCTCTTC | 7525 |
rs533034529 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:765590 | TTTTTAGTAGAGACA[C/T]GGTTTCACCTTATTG | 7525 |
rs533100696 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:760363 | TAGTCCCCGCTACTC[A/G]GGAGGCTGAGGCAGA | 7525 |
rs533114590 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:806331 | TCATATTAGAAATAT[A/C]AAAATGACCTTTAAA | 7525 |
rs533117143 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:726280 | AATACAAAAAATTAG[C/G]TGGGCGTGGTGGTGG | 7525 |
rs533144835 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:744193 | AACTTTCCCCTAAGG[C/T]CCTGCAGTTAGTAAA | 7525 |
rs533149367 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:757682 | CAAAAATTAGCTGGG[C/T]GTGGTGGTGCACACC | 7525 |
rs533157967 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:793342 | CCGCGCCTGGCCATT[A/G]TAATTATTACCTGAA | 7525 |
rs533164056 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:785528 | TGGTAGTAGGGCTGT[C/G]GTTGGCATTACATCC | 7525 |
rs533179510 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:800107 | GAAATTCATCCTGAG[C/T]GTTAATGATACTAGT | 7525 |
rs533246934 | snp | A/C/T | 0.000115305 | 0.00759217 | synonymous-codon | YES1 | GRCh38.p7 | 18:756699 | CTTTGCTGAAGATGA[A/C/T]GGACATGGTGACACT | 7525 |
rs533370323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:786952 | GGAATGGTTCAGTCT[C/T]TGATTAGGTAGTTAT | 7525 |
rs533374652 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:764051 | CATGAACCCGGGAGG[C/T]GGAGCTTGCAGTGAG | 7525 |
rs533406141 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:767103 | CTTCTGTAAGTCAGG[C/T]CTATCAAGCCATTTT | 7525 |
rs533416575 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:772728 | TGAGGCACCACGCCC[A/G]GCCAGCATCTCTATT | 7525 |
rs533437963 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:794126 | TGTTCATTTTGTGGT[A/G]ATGAAACCTGACAGA | 7525 |
rs533464184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:749616 | ATCCCAGCACTTTGG[A/G]AGACCGAGGCAGGCG | 7525 |
rs533537550 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:767668 | TAGCTTTACTGTGTC[C/T]TGAAATTATATAATA | 7525 |
rs533540246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:781951 | TTTATAAACATTATC[A/G]GAGTGCCTCATGGAA | 7525 |
rs533555561 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:726253 | ACATGGTGAAGCCCC[A/G]TCTCTACTAAAAATA | 7525 |
rs533572639 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:727786 | TCGGTAAGATTTTTT[A/T]TTGTTGGTGTTTTAG | 7525 |
rs533593516 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813676 | TAGCTACTAAAACTT[A/C]ATTTGTCATTGACTG | 7525 |
rs533672533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:781404 | CTCCCTCTTTCCTTA[C/T]GCTTGGCTTGTGACT | 7525 |
rs533696717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:802490 | CAGAGGTTGCAGTGA[A/G]CGGAGACCACACTAT | 7525 |
rs533697395 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:732636 | ACCCTGTCAAGGATC[A/G]TGGCTTTCACTGACT | 7525 |
rs533698578 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:809260 | GAACTTTATTTAGAA[A/T]TTTTTTCCCAAAAAT | 7525 |
rs533710206 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:738173 | AGTATAAAGCTTTTC[C/T]GAATTGTCAGATTCT | 7525 |
rs533724351 | snp | A/G | 5.18309e-05 | 0.00509046 | intron-variant | YES1 | GRCh38.p7 | 18:739711 | ACTTTTAATTCAAAT[A/G]GATACATGTATATAT | 7525 |
rs533757571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:803229 | GTCAGAGTGAGACTC[C/T]GTCTCAAAAACAAAA | 7525 |
rs533796541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:763954 | GCGAAAACCCGTTTC[C/T]ACAAAAAATAGAAAA | 7525 |
rs533880560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:808631 | TTCACACAACAAAGC[A/G]TGCACCACAAACATC | 7525 |
rs533958470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:791347 | TTGCAATCTTATTAA[A/G]AATAGTAACAGATAA | 7525 |
rs534027824 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:757516 | TCAAAAAAAAAAAAA[A/T]AAGAAAGAAAAAGTA | 7525 |
rs534030920 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:769308 | TGTGACTGTACTAAA[C/T]TCTTATGATTTCTAG | 7525 |
rs534073731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:734300 | TGGCTCACGCCTGTA[C/T]TCCCAGCACTTTGGG | 7525 |
rs534080953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:735179 | AAAAAAAAAAATCAT[C/T]ATATGAAAAAGATAC | 7525 |
rs534203675 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:782783 | CACTGCAACCTCCAC[C/G]TCCTGGGTTCAAGTG | 7525 |
rs534218359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:754263 | CAATCCCATATAATA[C/T]AATTCTCCCCTCTGT | 7525 |
rs534221922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:747406 | CCTGGGAGGTAGAGG[C/T]TGCAGTGAGCCGAGA | 7525 |
rs534222696 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:780965 | TAAAGTCCAAACTCC[A/T]TAACATAAAATAGAA | 7525 |
rs534233972 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:746994 | TCAAATACTTCAGTG[A/T]GTACTTGCTAAAAGA | 7525 |
rs534241658 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:741162 | CTCGGCCTCCCAAAG[C/T]GCTGGGATTGGAGGC | 7525 |
rs534298834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:735838 | AAAAAAAAAGTGGCA[A/G]CTAAATTAGGCCCTA | 7525 |
rs534312545 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:753721 | AAACTCCTGACCTCA[A/G]GTGATCTACCTGAGT | 7525 |
rs534353459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:749682 | AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAA | 7525 |
rs534388439 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776251 | CAGGCTGGAGTGCAG[A/C/T]GATGCAATCTTGGCT | 7525 |
rs534391068 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724293 | GGTTTTGTGCAACCA[C/T]ATCTGGGATTCCAGT | 7525 |
rs534398844 | snp | A/G | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:721739 | AATAGCAACTAAAAC[A/G]ATTAATAGGTGCATT | 7525 |
rs534440692 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:756366 | ATCACCATCAGGTTA[A/C]TACCAATTTTCCAGA | 7525 |
rs534460466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:799766 | ATTAGCTGGGCATGG[C/T]GGCATACACCTGTAA | 7525 |
rs534530434 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775746 | AGGCTACAGTGAGCC[A/G]TGATTGTGCCACTGC | 7525 |
rs534628844 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:739536 | AGAGCCCAAGAATTC[A/G]AGGCTCTTCAAGCAC | 7525 |
rs534663314 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:760458 | CTGGGTGAAAGAGTG[A/C]GATTCTGTCTAAAAA | 7525 |
rs534670942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:755822 | TCTACCTTTTTAAGC[C/T]AGCTATACTTTGTTA | 7525 |
rs534685710 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | YES1 | GRCh38.p7 | 18:761784 | ATAGGACCCATCATT[A/G]CTGCTCATCTCATTT | 7525 |
rs534688818 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:730507 | GAGTCACCACGCCCA[A/C/G]CTGGAATTTTAAAGC | 7525 |
rs534689962 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:728144 | ATTTTGAGACCATCC[C/T]GGGCAACATGGTGAG | 7525 |
rs534739203 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:762207 | TGCCTGTAATCTCAG[A/C]TACTCAGGAGGCTGA | 7525 |
rs534751129 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:781155 | GCACCTATAATCCCA[C/G]CTACTCAGGAGGCTG | 7525 |
rs534778280 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:766652 | CTTTGTGGTTTTTAC[A/G]TTTCCCTAATGACTA | 7525 |
rs534806094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:779850 | CGTACTCTTCTTTAA[C/T]TGGGGTTTTAAACTT | 7525 |
rs534809727 | in-del | -/AGTAAC | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:778442 | TGTTGCCTTATTATT[-/AGTAAC]AGTGACTAAAAATTT | 7525 |
rs534823854 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:733229 | TTAAGAAAATAGAGG[C/T]TGAAGCTCTAGTAAG | 7525 |
rs534836033 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:727172 | AGCTATGTAGTTACA[C/T]AGCTCATTTTGGATT | 7525 |
rs534846439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:787666 | AGTGAGCTGAAATCG[C/T]GCCACTGCACTTCAG | 7525 |
rs534858196 | in-del | -/ATA | | | intron-variant | YES1 | GRCh38.p7 | 18:773657 | AATCCTGTCCATTGT[-/ATA]ATAACTTTCCTGCTT | 7525 |
rs534863824 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:745422 | AAATATTTGCTTTTA[G/T]GTTTATTTTCATAAG | 7525 |
rs534911910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:750223 | TATACTAAGCACTTT[C/T]AGATACACAAACCAA | 7525 |
rs534938907 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:745118 | TCCCCTCTCCTAGTA[C/T]TAATCATGTAAAGAC | 7525 |
rs534943440 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:757304 | GTCAGGAGATTGAGA[C/T]CATCCTGGCTAACAC | 7525 |
rs534950468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:786303 | GTCACAATATCAAAC[A/G]TGGAGACTTTTTCCC | 7525 |
rs534951082 | in-del | -/C | | | intron-variant | YES1 | GRCh38.p7 | 18:806554 | TGCCCAGAACCACAT[-/C]CCTACATACAATTCA | 7525 |
rs534981890 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722286 | GGTAGAGAGTGTCAA[C/T]ACTAAGCAGGTTACG | 7525 |
rs534983728 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:807462 | TGTGACTGCACCACT[A/G]CACTCCAGTCTGGGC | 7525 |
rs534986996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:727970 | TTCCGATTTTGGATT[C/T]TTTTGGATTTTGGAA | 7525 |
rs535005543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:767324 | CTGGCTCATTTTTGT[A/G]TTTTTTTGTAAGGAC | 7525 |
rs535025235 | snp | C/T | 0.00517822 | 0.0506191 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722809 | CTTTAGAAGTGAATG[C/T]AGGCTGGGCGCGGTG | 7525 |
rs535027783 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:751382 | ACACCATCTGGTACT[C/T]AGAAAAATAGGAGCA | 7525 |
rs535046622 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:759312 | CTCTATTAAAAATAC[-/A]AAAAATTAGCTGGGC | 7525 |
rs535065731 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:764045 | GAATGGCATGAACCC[A/G]GGAGGCGGAGCTTGC | 7525 |
rs535092129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:773401 | GATGGGGCAAGTTCT[C/T]AGGAGCAGAGAAGTA | 7525 |
rs535126613 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:808738 | AATGCAAAGCCACAA[C/T]ATCAACCACTAAAAT | 7525 |
rs535129205 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:793407 | AGTGGCATGATCATC[A/G]CTCACTACAGCTTCG | 7525 |
rs535152775 | in-del | -/T | 0.00755907 | 0.0610114 | intron-variant | YES1 | GRCh38.p7 | 18:725594 | GTACTGTCATCTTCA[-/T]TAAGTGAAATCTGGC | 7525 |
rs535175179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776180 | TGCTTTACATCATCA[A/G]TACTTGGTATACTCG | 7525 |
rs535175889 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:795687 | GTATGTTCTCACTTA[A/T]AAGTGGGAGATGAAC | 7525 |
rs535184443 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:811200 | TATATACATAATAAA[C/T]GGACATAAAATTGTG | 7525 |
rs535226045 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:791686 | TATTTAACCTACTAT[A/G/T]TCAAAAATGTTATCA | 7525 |
rs535241596 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:788534 | GTATGGAAGTTTCCA[C/T]CCAGAAAGGCACTAA | 7525 |
rs535282350 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:792279 | ACTGTACTCCAGCCT[A/G]GATGACAGAGTGAGA | 7525 |
rs535319917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:754910 | CCATCAGAACAGAAA[C/T]TTTGTCTTGCTCACC | 7525 |
rs535324446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:758949 | AAGGTCATTCTTATT[C/T]GTATAGTTTTTCCCT | 7525 |
rs535366420 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:759963 | GAACATGCAGTGTTT[G/T]GTTTTCTGTCCTTGT | 7525 |
rs535377495 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:759351 | GGGCGCCTGTAATTC[A/C]AGCTACTTGGGAGGC | 7525 |
rs535422360 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:804331 | AAAAAATCTGGGCTA[C/G]GCACAGTGGCTCACG | 7525 |
rs535469595 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:783619 | TATCAATTTTTCTCT[-/T]TTTTTTTTTTTTTTG | 7525 |
rs535478591 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812781 | TTTGGGGCTTGCTTT[C/T]GTGGGGGAGGACGGG | 7525 |
rs535491549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:777751 | GGCGGAGGTTGCAAT[A/G]AGCTGAGATCACGCC | 7525 |
rs535507509 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:769504 | CCTTGGTTCTCAATC[C/T]TAAGAGGAAAGTATT | 7525 |
rs535521777 | snp | C/T | | | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721115 | CTGGTCATTCTATTT[C/T]ATATTCTTCACATAG | 7525 |
rs535621802 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:811877 | GGACTTGGGCGGGAC[A/C]CGGCAGGTCTGGACA | 7525 |
rs535644600 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:725831 | GGAGGTTGCAGTGAG[C/G/T]CGAGATTGCGCCATA | 7525 |
rs535750647 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:811546 | TCCGTAAAAGTGGAC[G/T]CTGAATGGTAAATTT | 7525 |
rs535761144 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:754445 | GGTGCGGTGGCTCAC[G/T]CATGTAATCCCAGCA | 7525 |
rs535783343 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:797829 | TCTCTTACTGGTAGG[A/G]CCCTGGAAGTATCAG | 7525 |
rs535803955 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:731724 | TGTAATCCCAGCATT[C/T]TGGGAGGCCGAGGCG | 7525 |
rs535827173 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:744806 | TTGGGATTAAAGGCA[C/T]AATCCACATGCCTAA | 7525 |
rs535832277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:738603 | GCTGAGGCGGGAGAA[C/T]TGTGTGAACCTGGGA | 7525 |
rs535839727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:777030 | CCACAAAAATCAGGG[A/G]GCAATTATTAATTTT | 7525 |
rs535879700 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:773541 | CCTGTACGAATTAAA[A/C]GGCTGGTAAGACAGT | 7525 |
rs535897454 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:767812 | TTCAAGTGATTCTCC[C/T]GCCTCAGCTTCCCAA | 7525 |
rs535972644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:742166 | AAAATCAGGCCTGTC[A/G]GCTTATCTGCTGACT | 7525 |
rs535979109 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:787531 | CCTGGCCAACATGGC[A/G]AAATCCCATCTCTAC | 7525 |
rs535980382 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:797783 | ATCATCTAATCATTC[C/T]TCTAAGATATCTACC | 7525 |
rs536012832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:728732 | GGTTTCACTACATTG[A/G]CCAGGATGGTCTCAA | 7525 |
rs536049547 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | YES1 | GRCh38.p7 | 18:798305 | AGCTATAAATTTATC[G/T]CTAAGAATCATCAAT | 7525 |
rs536069586 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:729077 | TGGGACTCCACAAAT[A/T]AGACCTTTTCACTAT | 7525 |
rs536098838 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:762113 | ATCACCTGAGATTGG[C/G]AGTTTGAGACCAGCC | 7525 |
rs536100746 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:760001 | TGCTCAGAATGATGC[C/T]TTCCAGCTTCATCCA | 7525 |
rs536104736 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:765777 | GCTAATAGTGTTAAA[C/G]ACAAAATCAAGTCAA | 7525 |
rs536109054 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | YES1 | GRCh38.p7 | 18:767010 | TATGGTTTATGTTTT[A/G]TGTGTCCGGAAAATT | 7525 |
rs536142014 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:814132 | TCTCTTCGCCCTCCC[C/T]TTTTTTTTTTATTAC | 7525 |
rs536150096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:736057 | TGCACCTGTAGTTCC[A/G]GCTACTCAGGAGGCT | 7525 |
rs536219771 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:745467 | ATGAACTCCAATGTA[A/C]ATACTATGCCAGTAA | 7525 |
rs536224428 | in-del | -/T | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722019 | CACATTAAGTTAGTG[-/T]TTTATCCCTACTATA | 7525 |
rs536225874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:770210 | TGATCTGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 7525 |
rs536245002 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:781376 | TACTGTTTTCATAAA[C/T]GCTTGGCACAACCTC | 7525 |
rs536304498 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:757363 | AAAAAATTAGCCGGG[C/T]GTGGTGGTGGGCGCC | 7525 |
rs536322169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:808595 | AACAATGGAAGATCT[C/T]ACTAAAACTTCCTGT | 7525 |
rs536345846 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:751317 | TAGATGGGTTCCTTA[C/T]CCAACTTTCTCCCCC | 7525 |
rs536356425 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:773932 | CACCTCCTGGGTTTG[A/G]GCAATTCTCCTGCCT | 7525 |
rs536356430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:745079 | TTGCAGCTAGCTGTC[A/G]TTGAAGACATTACCA | 7525 |
rs536407216 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:740604 | AACAAAGAGCAGAAC[A/C]GTGGGTTTATGCTGG | 7525 |
rs536490521 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:768772 | CAGTGGTGTGATCTC[G/T]GCTCACTGCAACCTC | 7525 |
rs536492632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:763186 | GTAGGACAGGCAGCT[A/G]GAGGAGATTTAATAT | 7525 |
rs536552055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:746903 | CTCTCTACATATGTA[C/T]GTGTGTGCATGTATA | 7525 |
rs536568819 | snp | C/T | 2.26657e-05 | 0.00336635 | intron-variant | YES1 | GRCh38.p7 | 18:739859 | AAGCAAATCTTATAT[C/T]AGGATTGAAATGAAT | 7525 |
rs536584307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:733989 | GTTTTATTTAAAAAG[C/T]GGCAGGTGGTTGGGC | 7525 |
rs536600695 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:796431 | ATTAGTTGCTGTTAT[A/C]ATGGTTATAATCAAC | 7525 |
rs536681256 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:752989 | GATATGAATTATAAA[C/G]TATAAATTCAAAAAC | 7525 |
rs536698698 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:763652 | AAGGCTGCAGTGAGC[A/T]GTGATCGTGCCACTG | 7525 |
rs536732440 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:811421 | CTGCCCCATGCCCAA[G/T]AAAGTGAAAGCTGGA | 7525 |
rs536737932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:731705 | AGGCACGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 7525 |
rs536760374 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | YES1 | GRCh38.p7 | 18:759875 | TCCCCCCACCCCACG[A/C]CAAGCCCCGGTGTAT | 7525 |
rs536766312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:757478 | ACTGCACTCCAGCCT[A/G]GGCGACAGAGCGAGA | 7525 |
rs536776062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:725731 | CGACTCTACAAACTA[C/T]AAAAATGAGCCAGGC | 7525 |
rs536794210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:805192 | ACTTACACAAACCTA[C/T]GTGGTATAGCTGACT | 7525 |
rs536842751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:785571 | TGATACTCTATGCTA[C/T]GGTTTGAATATGCAC | 7525 |
rs536936955 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:748919 | TAATCCCAGCACTTT[C/G]GGAGGCTGAGGCAGG | 7525 |
rs536950970 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:743228 | AATCCACAGCTAAAC[A/C]ATGACAGAAAACAAA | 7525 |
rs536981413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:790444 | AGATTTCTGTTTCTC[A/G]TTTCTAATTCATTAC | 7525 |
rs537007187 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:799183 | GTGGTATTTTCCATA[C/G]AGATGTCTAACTTGT | 7525 |
rs537032488 | in-del | -/TTTTTTTT | 0.193966 | 0.243639 | intron-variant | YES1 | GRCh38.p7 | 18:744690 | CCACCACGCCTGGCC[-/TTTTTTTT]TTTTTTTTTTTTTTT | 7525 |
rs537067836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:799696 | CAACAGAGCGAGACT[C/T]CATTTCAAAAAAAAT | 7525 |
rs537069423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:792992 | GCATCACAGCTTAAT[A/G]GCAAACAATAGAAAG | 7525 |
rs537085656 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:766492 | GTTTTCGTATTTATG[C/G]AAGTATTCCCAACTC | 7525 |
rs537105118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:759453 | GCCTGGGCGACAAGA[A/G]CGAAACTCCGTCTCA | 7525 |
rs537112777 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:772259 | GTCTCAAACTCCCAA[A/C]CTCAAGTGATCCTCC | 7525 |
rs537119525 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:746494 | ATGTGTGGGTTTAAT[A/T]TAATAAGGTTTTGTG | 7525 |
rs537120602 | in-del | -/ACAC | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:754940 | CTCTCCATACCTGAT[-/ACAC]AGACACTGAGTGTAC | 7525 |
rs537147744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:737062 | TCACTGAAAATCATA[C/T]TATTTTAGAAGGAGA | 7525 |
rs537161533 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:755489 | ACTCCTGAGCTCAGG[C/G]AATCTGCCTGCCTCA | 7525 |
rs537184426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:732094 | AGAAATAAAACAAGA[A/G]AAGAATCTCAAAATA | 7525 |
rs537259465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:794961 | GCTCGAACTACAGGC[A/G]CGTGCCACCATGCCT | 7525 |
rs537293139 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:747740 | TTCGTTTATGATCCT[A/C]CTCTAAGTGAATAGT | 7525 |
rs537302117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:761758 | TTCCACCAGCACCCC[A/G]GTATCAATGCATAGG | 7525 |
rs537303767 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:777228 | AACAGAGCCTATGAC[A/T]CAAGGATCTTCTATT | 7525 |
rs537322857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:806572 | TACATACAATTCAGA[A/G]TTTATTTAGTATTTA | 7525 |
rs537340846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:756339 | ATAATTAATGACATG[A/G]TCCAGTACATAATCA | 7525 |
rs537350853 | in-del | -/AGGGC | 0.46885 | 0.12085 | intron-variant | YES1 | GRCh38.p7 | 18:730956 | ATCAGAGAAGGGTGA[-/AGGGC]AATCAGCAAAGGAGT | 7525 |
rs537366578 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:762136 | GACCAGCCTGACCAA[C/T]GTGGAGAAACCCTGT | 7525 |
rs537379402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:793465 | TCTCAGCCTCCTGAG[C/T]AGCTAGGGCTACAGG | 7525 |
rs537382341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:800523 | ATGCTACAAAAATTA[A/G]GCTAGTATTCCCGCT | 7525 |
rs537394515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:734764 | GGTGGGAATGTAAAT[C/T]AGTACAACCACTATG | 7525 |
rs537421902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:798038 | CAAATTCTGCATTTG[A/G]GGAAATCACAGGGGT | 7525 |
rs537427787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:732658 | TCACTGACTTACCCG[C/T]CCAATGCCACAGTTA | 7525 |
rs537490569 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:769461 | CTCCAGTGCAATGTC[C/G]AACACAAGTGAGGAG | 7525 |
rs537505963 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:788657 | GGTGCAGTGGCTCAC[A/G]CCTGTAATCCCCGGC | 7525 |
rs537511922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:782640 | AATCTTATATGAATG[A/G]GAAATGTGTGACATC | 7525 |
rs537518608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:779746 | TTACTTCCAGTCTTT[C/T]GTCAAGATTTTTGAC | 7525 |
rs537543627 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | YES1 | GRCh38.p7 | 18:812118 | CGGGTCCTTACCTGT[C/T]CTCCGGCCGCGCTCT | 7525 |
rs537672504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:797734 | CAAAGGCAACTTTCA[A/G]TGTCTGCATTTATTA | 7525 |
rs537672892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:758829 | TCATCGCTTACCTAC[C/T]GTATTATCTATCATA | 7525 |
rs537764995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:764311 | CACTACAACCTCTGC[C/T]TCCTGGATTCAAGTG | 7525 |
rs537789231 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722180 | GAAAAATTACAATAT[A/C]ATAGTTCACATAAAG | 7525 |
rs537793114 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:729195 | GAATCCACTAATCTT[C/G]TCTTCTATTATGCCC | 7525 |
rs537798067 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:809930 | TATCACAATCTCCTC[C/T]CTCTTCCCATATATT | 7525 |
rs537872491 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:790592 | ACACAGTATTAGGTA[C/T]GAGAAGGGTACTAGA | 7525 |
rs537960122 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:734329 | GGAGGCCGAGGTGGG[C/T]GGATCATGAGGTCAG | 7525 |
rs537985120 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:791593 | GTGAACCACAAATAC[A/T]AACCACATATGCAAT | 7525 |
rs538022948 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:730980 | AAGGAGTGATTATAC[A/T]GCTTCACTAGGGAAT | 7525 |
rs538059790 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:725180 | TCCTTTGTAATCCCC[C/G]CTTCCTCAACCCCCT | 7525 |
rs538065696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:753756 | CTCCCAAAGTGCTAG[A/G]ATTAAAGGTGTGAGC | 7525 |
rs538075418 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:806581 | TTCAGAATTTATTTA[G/T]TATTTATTGTGCTAA | 7525 |
rs538095488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:763990 | GCGGGGTGTGGTGGC[A/G]GGCACTGTAGTCCCA | 7525 |
rs538128375 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:809377 | CTATCTTAGCTCACC[G/T]CAATCTCTGTCTCCC | 7525 |
rs538128741 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:729752 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 7525 |
rs538155606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:742111 | ATATTATTGGTTCAA[A/G]AGTAAAAATAATAAT | 7525 |
rs538188832 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:803400 | CCAAAGTGAGGTGAA[C/T]GGGTGGGAAATAAAA | 7525 |
rs538192723 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:735633 | GCAGGAGAATCGCTT[C/G]AATCTGGGAGGCGGA | 7525 |
rs538205512 | snp | A/T | 1.65575e-05 | 0.00287724 | intron-variant | YES1 | GRCh38.p7 | 18:747903 | AATAATTAATAAAAT[A/T]TGAAGTAGTGCCATA | 7525 |
rs538227283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:783613 | TACATGTATCAATTT[C/T]TCTCTTTTTTTTTTT | 7525 |
rs538344348 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:747427 | TGAGCCGAGATCACG[A/C]CACTGCACTCTAGCC | 7525 |
rs538388536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:794301 | TGAGGAAACATCAAA[C/T]AAAAACTCATCGATG | 7525 |
rs538400712 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:810927 | CATTCAAAATGCTTC[C/T]TGTCCACCGTGTGCC | 7525 |
rs538418099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:771137 | TGGGAGGCCCAGGCA[A/G]GCAGATCACTTGAGG | 7525 |
rs538442119 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:771151 | AGGCAGATCACTTGA[C/G]GTCTCAGGAGTTCAA | 7525 |
rs538478864 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:764858 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 7525 |
rs538480959 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:738875 | GTTGCTCAGGCTGGA[A/G]TGCAATGGCGAGATC | 7525 |
rs538528261 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:725610 | TAAGTGAAATCTGGC[C/T]GGGCACAGTGGCTCT | 7525 |
rs538534034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:737978 | GCACAGCCTGGTTTT[C/T]ACATTTTTAAAGGGT | 7525 |
rs538544075 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:762340 | AAAAGAAAAAAGAAA[C/T]GTAACATCATTTAAA | 7525 |
rs538633180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:787407 | CCAGCTGATACATAC[C/T]GTATTTAAAAAAATT | 7525 |
rs538642792 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:779971 | GGGTGCAGTGGCTCA[A/C]GCCTGTAATCCCAGC | 7525 |
rs538667897 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:747008 | GTGTACTTGCTAAAA[A/G]AGAAGGATACTTTCC | 7525 |
rs538705910 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:777519 | CTATCAGAATTACTT[A/C]TATCAGGCCGGGTGC | 7525 |
rs538709899 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:762308 | CTGGGCAACAAGAGC[A/G]AAACTCCATCTCAAA | 7525 |
rs538737508 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:733919 | GTTTTAAAACAGAGT[C/T]CTTTAGATATTTAGA | 7525 |
rs538744189 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:807647 | TAGCTGATAACGTAT[G/T]TGCAACTGTTGATGT | 7525 |
rs538772878 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:728507 | GTCAATGCTCAAAAA[C/G]TTTTGGATTTTGGAG | 7525 |
rs538876857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:768642 | TATGACGGTGGTCCC[A/G]TAAGATTATAATACT | 7525 |
rs538882409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:746345 | AGCAAAATAACAGAC[C/T]CTTTCTGTCAGTGAC | 7525 |
rs538894297 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:780527 | AAGAAAGCCCTTCTC[A/G]TATGCCACCCCATGA | 7525 |
rs538935737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:752047 | TAAACTCTCCGAAGA[C/T]CTTCCATAAAACTAC | 7525 |
rs538938436 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:738507 | CATCCTGGCGAACAC[A/G]GTGAAACCCCGTCCC | 7525 |
rs538953249 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:757444 | GGAGGCGGAGCTTGC[A/G]GTGAGCAGAGATCGC | 7525 |
rs538970581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:752869 | AATCGCTTGAAACCC[A/G]GAAGTGGAGGTTGCC | 7525 |
rs538987264 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722872 | CCGAGGCGGGCAGAT[C/G]ACAAGGTCAGGAGAT | 7525 |
rs538991783 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:788714 | CACTTGAAGCCAGGA[A/G]TTTGAGACCGGCCTG | 7525 |
rs539045407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:764835 | CCTCCTGGGTTCATG[C/T]GATTCTCCTGCCTCA | 7525 |
rs539057864 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:795747 | ACATCACACACTGGG[A/G]CCTGTTAGGGGGTGG | 7525 |
rs539058121 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:802256 | CCATCTCTCTTAAAA[A/C]AGAAAGAAAATAAAA | 7525 |
rs539089333 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:767920 | TGGCCAGGCTGGTCT[C/T]AAACTCCTGACCTCA | 7525 |
rs539132360 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:771059 | AACATTTCATTCCCC[A/G]GTGTTAATAATCATT | 7525 |
rs539171894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:808030 | TGAGGCACAGAGGCT[C/T]GTAACTCAGTCCATT | 7525 |
rs539178815 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:730968 | GTGAAATCAGCAAAG[G/T]AGTGATTATACTGCT | 7525 |
rs539203448 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:810822 | ATATTATTTGCTAAA[C/G]TAAAACTTTCTTACT | 7525 |
rs539251641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:792947 | ATCCTTCCATGATAT[C/T]ATATATCTATAAAGT | 7525 |
rs539261848 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:784907 | ATATTCAAAGGTTCC[A/G]AGAATTCACAGAACA | 7525 |
rs539289492 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | YES1 | GRCh38.p7 | 18:748798 | TTACTCATTTTAGAT[A/T]AAAAAAAAAATCACA | 7525 |
rs539311277 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:754996 | CCTAATAGAATATTT[C/T]ATATAAGTAAATTGC | 7525 |
rs539427951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:778663 | TCCTAGAAAAATAAA[C/T]TTAGAGACTTAACTT | 7525 |
rs539459135 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:798430 | ACATTTGTTATGAGT[C/T]TCTCCTTCTGACTTA | 7525 |
rs539461100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:805094 | CCTTAAAATTTTATC[A/G]ATACGGTCATGCATC | 7525 |
rs539462168 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:735177 | AAAAAAAAAAAAATC[A/G]TTATATGAAAAAGAT | 7525 |
rs539489413 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:772215 | TGTATTTTCAGTACA[C/G]ACAGCGTTTCTCCAT | 7525 |
rs539492402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:764502 | GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCCT | 7525 |
rs539515699 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:777816 | TGGCTTAAAAAAAAA[A/G]AAAAAAAAAATTAAA | 7525 |
rs539550495 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724157 | AGCCTCACTGTCCTT[C/T]ATTACCATGCTGTCA | 7525 |
rs539590860 | in-del | -/AATA | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:744014 | TAGTATGTATATACT[-/AATA]TATAGTAGATATGTT | 7525 |
rs539603068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:799884 | AACGAGACTCTGTCT[C/T]AAAACAAACAAACAA | 7525 |
rs539629302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:760566 | AATACATGCCATTTT[A/G]TATCATGGACTTGAG | 7525 |
rs539665163 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:800488 | TGAAGGAGTTGTACT[A/G]TAGATATTGTGGGAT | 7525 |
rs539727165 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:811959 | CCGCCGGGCGATCCG[C/G]GGGAGGGGAGAAGTT | 7525 |
rs539753474 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:792324 | ACAAACAAACAAATA[A/C]ATAAAGAAGTCATAT | 7525 |
rs539775755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:726447 | CAAAAACAAAAACAA[C/T]TTCACTCTTCAGAAT | 7525 |
rs539795811 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:811608 | TTAAACATGTTGCGG[G/T]TTTCAATCAAACCAA | 7525 |
rs539877648 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:758189 | TTTCAACATGTAACC[A/G]ATATAAACATTTTAA | 7525 |
rs539889856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:785514 | AAAGGTCTGAATTCT[A/G]GTAGTAGGGCTGTGG | 7525 |
rs539895895 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:733840 | AAGTTTATAAACTTA[C/T]TGCAGAAATAATATT | 7525 |
rs539931697 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:743703 | ACGAGGTCAGGAGTT[A/C]GAGACTAGCCTGGCC | 7525 |
rs539975023 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | YES1 | GRCh38.p7 | 18:765134 | CACCTACATACAAGC[A/G]TAAGACAGGGAGAGA | 7525 |
rs539990944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:726986 | TCGGTCCACGCTACA[C/T]GTGGAAAGTTCTTTC | 7525 |
rs540009308 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:759343 | GAGGTGGCGGGCGCC[A/T]GTAATTCCAGCTACT | 7525 |
rs540011698 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | YES1 | GRCh38.p7 | 18:751295 | CTTAATTTCATCAAT[C/T]GGAAAGTAGATGGGT | 7525 |
rs540042040 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:751629 | TCATCTCTGGATCAT[C/T]AACCAGCTCAGTGGT | 7525 |
rs540086231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:756499 | GACAAGCCTTAAGTA[C/T]ATATTACCCAAGGTG | 7525 |
rs540087431 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:758019 | TGTATTCTGTCTATA[C/G]CAGGACTATGTCAAC | 7525 |
rs540098095 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:784210 | TTATTGTTTTCATTA[A/C]AAGTTTTCTATATGC | 7525 |
rs540155101 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:786602 | CCAAAATTAATACCA[-/T]TATCAGTTCAGGGTG | 7525 |
rs540182925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:728146 | TTTGAGACCATCCTG[A/G]GCAACATGGTGAGAC | 7525 |
rs540188109 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722891 | AGGTCAGGAGATCGA[C/G]ACTATCCTGGCTAAC | 7525 |
rs540207608 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:795362 | GAAACATAAAGGAAA[C/T]GTGACAAAATGTTAA | 7525 |
rs540220225 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:767573 | TAACCATGTATGTGT[A/G]TAGGTCTGCTTTCAT | 7525 |
rs540243914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:762645 | ATTAAAAAAAACTAT[A/G]TACTGGGTACAACGT | 7525 |
rs540270210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:740013 | GAAAACTTCTGATAA[C/T]ACATGCAAAAAAAGA | 7525 |
rs540271890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:734187 | GGGAGGCTGAGGCAG[A/G]AGAATTGCTTGAACC | 7525 |
rs540309626 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:738641 | CTTGCAGTGAGCCGA[G/T]ATTGCACCACTGCAT | 7525 |
rs540331089 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:739439 | CTGTGTCTACAAAAA[A/T]AATAATTTTTTAAAT | 7525 |
rs540342544 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:759981 | TTTCTGTCCTTGTGA[C/T]AGTTTGCTCAGAATG | 7525 |
rs540381212 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | YES1 | GRCh38.p7 | 18:795944 | ACACACACACACACA[C/T]ATAAGACCTATGAGT | 7525 |
rs540402423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:790092 | ATAAACAAAAGATTC[C/T]CGGCTGAGTGCAGTG | 7525 |
rs540467471 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:752390 | GCTGGGATTACAGAC[A/G]TGAGCCACTGTGCCC | 7525 |
rs540505197 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:757317 | GACCATCCTGGCTAA[C/T]ACGGTGAAACCCCGC | 7525 |
rs540623082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:774516 | CGATAAATGTTAACG[C/T]CATTCTTCTAGTTTT | 7525 |
rs540623391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:782214 | CATTCTTCTCTCCTG[C/T]GGCACAATGGCCTTT | 7525 |
rs540661244 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:765993 | ATTATCAAGATGTTT[C/G]CTATCATTTCTTTGT | 7525 |
rs540729224 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:748326 | AATAAAACAATTTGG[G/T]AGGTAAATCTTTCAA | 7525 |
rs540761236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:781710 | TGGTTCTGTCACTTA[C/T]TAGCTACTGTGATCC | 7525 |
rs540765900 | in-del | -/TTTTTTTTTTTTTTTTTTTT | 0.422 | 0.181428 | intron-variant | YES1 | GRCh38.p7 | 18:787081 | GTGATACATACTGTC[-/TTTTTTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTG | 7525 |
rs540771883 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723005 | GCTGAGGCAGGAGAA[G/T]GGTGTGAACCTGGGA | 7525 |
rs540838338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:760314 | GCCTCTACTAAAAAT[A/G]CAAAAGTTAGCCACG | 7525 |
rs540864112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:765544 | GCTGGGATTACAGGC[A/G]TGTACCACCACACCC | 7525 |
rs540907693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:736428 | GCAGTAGCCCCCAGG[C/T]TGTAACCACCAAAAA | 7525 |
rs540939076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:808930 | TGAGATTTCATGGCA[C/T]TCTTAAGAATAGAAA | 7525 |
rs540983978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:777401 | TCCAAAAAGCCAAGC[C/T]TAACAAAAATTCTAG | 7525 |
rs541008178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:734911 | GCCTGTAATCCCAGC[A/G]CTTTGGGAAGCCAAG | 7525 |
rs541013973 | snp | A/G | 3.29457e-05 | 0.00405854 | missense | YES1 | GRCh38.p7 | 18:756656 | CAAATGGTGTCATGG[A/G]AAGACTGCTGAAATT | 7525 |
rs541023797 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:793983 | ACTACTAAACTTGGA[G/T]TAAGAGAGCTACACA | 7525 |
rs541049266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:778185 | CTCAAGGACAGGGGG[C/T]TAAAAGTAGGCAAAA | 7525 |
rs541101787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:761063 | CAAGAAATGCACATT[A/G]TAAGAAGATACCTTT | 7525 |
rs541123058 | in-del | -/C | | | intron-variant | YES1 | GRCh38.p7 | 18:804939 | AACACAAACCAAAAA[-/C]CTAGCATAGTAGTAT | 7525 |
rs541163650 | in-del | -/AAAT | | | intron-variant | YES1 | GRCh38.p7 | 18:733183 | AGCTGATGATATAAA[-/AAAT]AAGTTGGCTGTGGGA | 7525 |
rs541198694 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | YES1 | GRCh38.p7 | 18:812256 | ACGGCAGAGCCGGCC[C/T]GGGACGCGTTACTTC | 7525 |
rs541203119 | snp | A/T | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722954 | AAAACTAGCCAGGCG[A/T]GGTGGTGGGCACCTG | 7525 |
rs541212215 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:800067 | ACCTTAGTTTCTCCA[A/T]CAGACTCAAGTAGAA | 7525 |
rs541216304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:772319 | CAGGCATGAGCCACC[A/G]CACCCGGCCTGCATG | 7525 |
rs541245905 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:780809 | TGGATTATTGCAAAA[C/G]CCTCTTTAACTGACT | 7525 |
rs541257451 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:775007 | GAACAGTTAAGAGCA[C/T]AGAGGTCAGAGACAG | 7525 |
rs541286798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:773198 | TTTCTTTAATAGAGA[C/T]GAAGTCAAAAATCTG | 7525 |
rs541317054 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:772502 | CAATGGTGCGATCTC[C/G]GCTCACTGCAACCTC | 7525 |
rs541323522 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:744126 | CCACTATTGTGCTAA[A/T]TTAGCACTTCACAAG | 7525 |
rs541329525 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:802726 | TCCCAGTTCTGCCGG[C/T]TGTGTGACCTTAGCA | 7525 |
rs541334916 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:740954 | CCAGGCTGGAGTGCA[A/G]CGGTGTCATCTTGGC | 7525 |
rs541369591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:786840 | ATTTACATTTTAATA[C/T]ATATACGGCATCTTT | 7525 |
rs541384377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:800647 | TAAGATGGTGAAGAA[A/G]ATTATTGTTAATGTA | 7525 |
rs541457934 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:728683 | GGTGTGTGCCACCAT[A/G]CCCAGCTAATTTTTG | 7525 |
rs541467221 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:786268 | AGATGGGGTGGGGGT[A/G]GGGGTTGACTTCCTT | 7525 |
rs541494557 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:763814 | TCAGTTAAATATGGA[A/C]AGAGGAGACATTAAG | 7525 |
rs541507204 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:726607 | CAACATGGCGAAACC[C/G]CCTCTCTACTAAAAA | 7525 |
rs541520675 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:806253 | CTAAAATAGTACAAC[G/T]TATTTATTTAAAATA | 7525 |
rs541520959 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:795604 | GTTCATGTCCTTTGC[A/G]AGGACATGGATGAAG | 7525 |
rs541567352 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:721592 | ACCACAAAGAATGAG[C/T]TCAATAATGTTCTGA | 7525 |
rs541582354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:782990 | CTCGGCTAACTTTCT[A/G]AATTTCTGATCTCAA | 7525 |
rs541590679 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:756093 | TGAGCTTTAGGATTT[C/T]TCTTTTTTAAATCAG | 7525 |
rs541620048 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:807794 | TATCCCTCTTGAAGG[A/C]CTTCCACTTCCTAGG | 7525 |
rs541643634 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:783661 | CACTCCTGTTGCCCA[C/G]GCTGGAGTGCAATGG | 7525 |
rs541668671 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:750680 | GGTGCTATGTAAACA[C/G]CTAAGAGAGATACTT | 7525 |
rs541680124 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:786197 | TAAATGAGAATTTGG[A/C]AGGAAGCTGGTCTCC | 7525 |
rs541704037 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:790179 | TCAGAAGTTTGAGAT[A/G]AGCCTGGCCAACATG | 7525 |
rs541709374 | in-del | -/A | 0.283421 | 0.247756 | intron-variant | YES1 | GRCh38.p7 | 18:785778 | TGTCTCTACAAAAGG[-/A]AAAAAAAAAAAAAAG | 7525 |
rs541715667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:753814 | GAATGTCTAATAAGC[A/G]TTTAAAATTTATTAC | 7525 |
rs541732806 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:744642 | TGATCTGTCTGTTTC[G/T]GCCTCCCAAAGTGGT | 7525 |
rs541767474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:790968 | TTTTTTTAAAGTCTA[A/G]GCTGGGTGCAGTGGC | 7525 |
rs541794110 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:757721 | CAGCTACTAGGGAGG[C/G]TGAGGCATGAGAATC | 7525 |
rs541850847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:810234 | CACCATCGGTTGGTA[A/G]TATTTCACTTATACA | 7525 |
rs541856853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:770758 | AAAGTCTAAAACCCA[C/T]TGTTTCATTATTTTG | 7525 |
rs541937794 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:782192 | TTGCTACTATGCTCA[C/T]GTGCTTCATTCTTCT | 7525 |
rs541937837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:808864 | CAAAACATATTCATC[C/T]TTCAGGTGCTGTGAA | 7525 |
rs541978776 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722988 | TCCCAGCTACTCGGG[A/G]GGCTGAGGCAGGAGA | 7525 |
rs541991487 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776394 | TTTTGGTGGGTGTGT[A/C]GGAGTCTCTCACTGT | 7525 |
rs542003017 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:811312 | TGCAGAAAATGATTC[A/G]ACCAAATCCGAACTG | 7525 |
rs542060072 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:749691 | AACCCCGTCTCTACT[-/A]AAAAAAAAAACAAAA | 7525 |
rs542088993 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:740918 | TCTTTATTTATTTGA[A/C]ACGGAGTCTCACTCA | 7525 |
rs542108810 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:804200 | TGATGATAGTGGCTA[A/T]TTTTCTCATATAATG | 7525 |
rs542120981 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:804700 | GGCGGATCACCTGAG[A/C]TAGGGAGTTGGAGAC | 7525 |
rs542176116 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:731780 | AGACCATCCTGGTTA[A/G]CACGGTGAAACCCCG | 7525 |
rs542250287 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:764672 | GTTTAAAGCTCAGAA[A/T]AAGATGGAAGCCAGA | 7525 |
rs542326582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:730251 | CTGAACTCTGCTCGA[C/T]TCCCCAGCCTCCTAG | 7525 |
rs542341078 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:769976 | TTTTTTTTTTGAGAC[A/G]GAGTCTTGCTCTATC | 7525 |
rs542341605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:737331 | GGTGGCACATACCTG[C/T]AGTCCCAGCTACTTG | 7525 |
rs542392749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:772518 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 7525 |
rs542425696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:759541 | TATCTATGAGTTCTG[C/T]ATCCATGGATTCAGC | 7525 |
rs542465716 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:732742 | ACTATGAGAAGAAAT[A/G]AAGGCCTTTTCCCCG | 7525 |
rs542503976 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:760738 | AAAAAATTAAAGGTA[A/C]GTAGTTTCATAATCT | 7525 |
rs542511581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:759192 | ATAACCGGGGCTAGG[C/T]GCGGTGGCTCACGCC | 7525 |
rs542515787 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:764890 | GGTGCACACCACCAC[A/G]CCCGGCTAATTTTTT | 7525 |
rs542558222 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | YES1 | GRCh38.p7 | 18:754142 | AAGAAAATTCAATCA[A/T]ATCCTTTACTTAATC | 7525 |
rs542561097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:800871 | TAAAAACAAAGGCTG[A/G]GTGTGGTGGCTCACG | 7525 |
rs542568142 | snp | A/G | 3.29462e-05 | 0.00405857 | missense, intron-variant | YES1 | GRCh38.p7 | 18:732915 | ACTTTATTGTAAACC[A/G]ACCATACAGTGCAGC | 7525 |
rs542616081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:781143 | GAGTGGTGGCAGGCA[C/T]CTATAATCCCAGCTA | 7525 |
rs542656088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:738719 | AAAAAAAAATTCAGC[A/G]TACACTTTAGATTAC | 7525 |
rs542657377 | in-del | -/ATCA | 0.00068047 | 0.0184329 | intron-variant | YES1 | GRCh38.p7 | 18:751807 | ATAGTAACACCACCT[-/ATCA]GAGGGAAAAAAGACC | 7525 |
rs542677799 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:765510 | TTCAAGCGATTCTCC[C/T]GCCTCACCCTCCCCA | 7525 |
rs542696113 | in-del | -/A | 0.00874735 | 0.0655527 | intron-variant | YES1 | GRCh38.p7 | 18:762502 | ATAAAAGATGGAAAG[-/A]AAAAAACAAACAATA | 7525 |
rs542706885 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776329 | CTCCCATGTAGCTGG[A/G]ATTACAGGCTCATGC | 7525 |
rs542727876 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:738093 | CAACCTCCCCTACCA[C/T]AGAGTGTCTAACTCA | 7525 |
rs542731487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:745259 | TAGGTTAATTTTCTA[A/G]GATAAGAAAAATGCA | 7525 |
rs542744293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:779992 | TAATCCCAGCACTTT[A/G]GGAGGCTGAGGAGGG | 7525 |
rs542756899 | in-del | -/TAAACCCGAGAT | | | intron-variant | YES1 | GRCh38.p7 | 18:798877 | CTGCTACTTTTAATA[-/TAAACCCGAGAT]GACATGACTCCTATC | 7525 |
rs542774788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:801222 | CCTGTGGTCGCAGCT[A/G]CTGGGGAGGCTGAGG | 7525 |
rs542811371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:768420 | ATGAATGTGGTATTT[C/T]ATTTATTTGGGCATT | 7525 |
rs542819587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:763477 | AGGTGGAAAGATTGC[C/T]TGAGCCTAGAAATTT | 7525 |
rs542823741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:768979 | AAGTGCTGGGATACA[A/G]GCATGAGCCACTGTG | 7525 |
rs542827334 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:762396 | GGATATTACACTGAT[A/T]ACCTGGGTAACAAAA | 7525 |
rs542852728 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:757312 | ATTGAGACCATCCTG[A/G]CTAACACGGTGAAAC | 7525 |
rs542895132 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:739327 | AGTTCTAAAATTCCA[A/T]TATTGGCCAGGTAAT | 7525 |
rs542909748 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:789575 | GCAAGAGAGCAAGAC[A/T]CTGTCTCAAAACAAA | 7525 |
rs542913729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:807741 | GCAAAATTCAGGCAG[C/T]CACCACGGATATGCA | 7525 |
rs543003016 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:788919 | TGACAGAGTTAAAGA[C/T]TGTCTCAAACAAACA | 7525 |
rs543030645 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:781599 | AATTTCTCTCTTGTA[A/G]CTTAGCCTAGTGTTG | 7525 |
rs543044066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:748243 | AATAAAGCCTCAAAA[C/T]CCTACACACTTAGTT | 7525 |
rs543063097 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:751570 | TGCATCTATAGAAGC[A/C]AATGCATCGTTAAAC | 7525 |
rs543072194 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:771525 | TCTGTTAAACCACTC[C/T]GTGGCATTTTTCTTT | 7525 |
rs543112763 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | YES1 | GRCh38.p7 | 18:756082 | TTTAAACTGTCTGAG[C/T]TTTAGGATTTTTCTT | 7525 |
rs543121058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:795221 | AACTGTACTGCAGTT[A/G]TATAAGAAAACGTCC | 7525 |
rs543165044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:728866 | CTCAATCTGCACCAC[C/T]TCCTTATGGCTGTTT | 7525 |
rs543183826 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:795806 | AATACCTAATGCATG[A/C]GGGGCTTAAGACTAG | 7525 |
rs543190120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:788009 | ACAGGAAAACAGCAC[A/G]TATATGAGAAAGGCA | 7525 |
rs543214815 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:786466 | ACTTTGCAACATTCA[C/T]TACTATAAACATCAT | 7525 |
rs543216070 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:764946 | TCACTATGTTGGCCA[C/G]ACTAGTCTCAAACTC | 7525 |
rs543367515 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:783815 | AAACGGGTTTCACCA[C/T]GTTGGCCAGGCTAGT | 7525 |
rs543372500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:735742 | AAACAAAAAAACCTA[C/T]ATATTGGGTACAGTG | 7525 |
rs543388548 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:777234 | GCCTATGACTCAAGG[A/T]TCTTCTATTTCCTTC | 7525 |
rs543393623 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | YES1 | GRCh38.p7 | 18:792587 | TGTGTGTGTGTGTGT[A/G]TATACATATATACAT | 7525 |
rs543404590 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | YES1 | GRCh38.p7 | 18:771055 | GAAAAACATTTCATT[C/T]CCCGGTGTTAATAAT | 7525 |
rs543417190 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:799457 | GCTCACGCCTGTAAT[C/G]CCAGCACTCTGGGAG | 7525 |
rs543431388 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:760206 | TGGGCACAGTGGCTC[A/G]CACCTGTCATCCCAG | 7525 |
rs543451502 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:741655 | GAAAAATACACAAAT[A/T]ATCTATGTGTGGTGG | 7525 |
rs543476887 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:765378 | AAATTATTTTTGTTT[G/T]AAGTATTTTATAATT | 7525 |
rs543518133 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:798091 | ATGAGCCTCACTCTG[A/G]GAACCACCTTCATGA | 7525 |
rs543563382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:736265 | TGAAAGAAAGCACTA[C/T]GTCTAAAGCAGGGTT | 7525 |
rs543627154 | in-del | -/TTGGCTTTT | 0.00597247 | 0.0543191 | intron-variant | YES1 | GRCh38.p7 | 18:727580 | TTTTTCTCTCCTCTG[-/TTGGCTTTT]TGTCTTCTCTTGTTA | 7525 |
rs543635747 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:752681 | GTCACAGTGGTTCAC[A/G]TCTGTAATCTCAGCA | 7525 |
rs543745446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:793785 | GTACTCAACAAATGA[C/T]AGGGATCTATCAAAA | 7525 |
rs543835699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:808733 | ACAACAATGCAAAGC[C/T]ACAATATCAACCACT | 7525 |
rs543840819 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:760801 | ACTTCCACATTGAGA[C/G]GGGCAGGGGTGGGGA | 7525 |
rs543867735 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:768337 | GGATTCTGACTGGGA[G/T]TATTCTTAATCTATA | 7525 |
rs543903506 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:757059 | TCTCCAACTCAATCA[C/T]CTTTAATAGTCCAAT | 7525 |
rs543909145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:763769 | ATAATGGGGGAAATG[A/G]GAAGTGTATAAGTAT | 7525 |
rs543930586 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:729561 | TATTGCTATTTTGAA[A/G]TCTTTTGCTAACTCC | 7525 |
rs543932608 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:725464 | TTTAGTTATTTTTTT[G/T]AGGAATAAGTGATTT | 7525 |
rs543969333 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:726000 | TGAGGGCTTACTATA[A/C]TTGAACTTCTTTTCC | 7525 |
rs543976964 | snp | C/T | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:721621 | GAATTTAATAAAGGA[C/T]TGATTAAATTCTGCT | 7525 |
rs544016471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:790871 | TCCAACAGATATCTG[A/G]GGTTATCAAAAGAGC | 7525 |
rs544072187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:799983 | ACAGAACTCCTATAT[C/T]GTAAGTGGGTGAATA | 7525 |
rs544082474 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:779151 | GGCAGTGGCTGATCC[C/T]AGCAGTTTGGGAGGC | 7525 |
rs544130074 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:757592 | TTGGGATGCCTAGGC[A/G]GACCGATCACTTGAG | 7525 |
rs544145657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:749777 | AGGCAGGAGAATGGC[A/G]TGAACCCAGGGGGCA | 7525 |
rs544150012 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:796541 | TTGGGAGACCGAGGC[A/G]GGCAGATCACAAGGT | 7525 |
rs544166989 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722896 | AGGAGATCGAGACTA[C/T]CCTGGCTAACACGGT | 7525 |
rs544177057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:763433 | GGTGTGGCGGCTCAT[A/G]TCTGTAATCTCAGCA | 7525 |
rs544202106 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:814235 | TCAATCTTACATTTA[A/G]TGGCTCACTTGTTTC | 7525 |
rs544212393 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:734440 | GGCAGGCACCTGTAG[C/T]CCCAGCTACTCGGGA | 7525 |
rs544239929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:734845 | ATCCAGCAAACCCAC[C/T]ACTGGGTATCTTCCC | 7525 |
rs544271106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775828 | AAAATAGAATCATAT[A/G]TAATGCATTATTTTG | 7525 |
rs544272110 | snp | A/C/T | 1.65721e-05 | 0.0028785 | intron-variant | YES1 | GRCh38.p7 | 18:733016 | TTAAAAATCTATTTG[A/C/T]GTAAACATAGCATAT | 7525 |
rs544285927 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:814270 | AATATTTTTTAAAAA[A/T]TTTTTTAATGAGGAA | 7525 |
rs544297996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:808283 | CCCTCTACTGTTACT[A/G]TAGCTCCTTTTGCTA | 7525 |
rs544321332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:728205 | ATGGCACACACCTGT[A/G]GTCTCAGCTACTTGG | 7525 |
rs544344674 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:790121 | TGGCTCATGCCTGTA[A/C]TCTCAGCACTTTGGG | 7525 |
rs544359474 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:728815 | AGGCCTGAGCCACTG[C/T]GCCCAGCTGCATTTC | 7525 |
rs544372861 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724268 | GTTTAATACTTGGGG[A/G]AAAAAAAGTGGTTTT | 7525 |
rs544402099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:740865 | GCCTTACCTTCATTA[C/T]ATTTCTTATGTTCCA | 7525 |
rs544445203 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:804168 | CTTTGTCAATTAAAA[A/C]AATTAAATGTAAATT | 7525 |
rs544446597 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:746569 | GAAGAAAGACAAAAG[C/G]ACAAAACAAAAAGTA | 7525 |
rs544472995 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:752525 | CAAACTAGTGGGGCA[C/G]TGTTCTTCATATAAA | 7525 |
rs544538998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:730554 | TTCCCTATGGTTCCT[C/T]CTCTGGGACCCTGTC | 7525 |
rs544580306 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:810201 | ATGCAAATTTCAACT[C/T]TGAATAAGTAAGTCT | 7525 |
rs544677142 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:740173 | TAGGAATATCTTGGG[G/T]GTGGTTAAAACTAAA | 7525 |
rs544677380 | in-del | -/TTAT | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:797929 | GCCTCTATTTTCTTA[-/TTAT]TTATTTGTTTTTAAT | 7525 |
rs544677828 | snp | G/T | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722224 | TCATGTCACAAGTTG[G/T]TGATAAGAGGAAATA | 7525 |
rs544744874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775296 | AAATTTAAAAAAAGT[C/T]ATTGAAATATAGTAC | 7525 |
rs544790356 | snp | A/G/T | | | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721260 | AATTGACCACAGGCC[A/G/T]GGCGCGGTGGCTCAC | 7525 |
rs544800096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:764623 | GGTTCGTTTTAGGTT[C/T]ATGCTGTGAAGTCTG | 7525 |
rs544851276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:761179 | TGTAAAAACTGGGAG[A/G]GGGAAAGGTCTACTG | 7525 |
rs544865923 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:737244 | GATCATTTGAGGTCA[C/T]GAGTTCGAGATCAGC | 7525 |
rs544883384 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:770634 | CCTGTCCCAGATCTA[A/C]AATTTAGAATGTGCC | 7525 |
rs544985177 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:806364 | CATATTTGAAGGACT[G/T]CTTAAGCTATTTTGT | 7525 |
rs544999102 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:794253 | GCCTTTAAGTGGTAC[C/T]CCTGCCTCAAATTCA | 7525 |
rs545026425 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:751503 | TGGCAGAACCACAGC[A/T]GCACAAATTGTAGAA | 7525 |
rs545026961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:772401 | AGAACTTATCGCTTC[C/T]CTACCATAATGTGGA | 7525 |
rs545050770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:757243 | GCGCAGTGGCTCACG[C/T]CTGTAATCCCAGCAC | 7525 |
rs545098638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:744781 | TCAAGTGATCCTCCT[A/G]CATCAGTAGTTGGGA | 7525 |
rs545113287 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:743914 | CTGACTCGAAAAAAA[A/T]AAAAATATATATATA | 7525 |
rs545113730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:750928 | AAGTAATTCAGTATG[C/T]CTGGGTATTAGAGTT | 7525 |
rs545117414 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:785779 | TGTCTCTACAAAAGG[A/G]AAAAAAAAAAAAAGC | 7525 |
rs545133255 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:746292 | GTGTCTCTCAAAACT[A/C]CACCTGACAGTCACA | 7525 |
rs545151173 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:778409 | TTGGAAACAGCACCC[G/T]GCCTGTCAGCATGAC | 7525 |
rs545185315 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:773715 | TTTTAGCAAACTTTG[C/T]TCCAACTTTCCTATG | 7525 |
rs545233421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:739239 | TGTGAATTTTAGATA[C/T]CTCTCATCTTTTGAT | 7525 |
rs545297472 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812899 | GTGAGCCGGGGGCGT[A/T]ACTCACACCCTCATC | 7525 |
rs545299033 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813679 | CTACTAAAACTTCAT[G/T]TGTCATTGACTGTCT | 7525 |
rs545380127 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:753952 | TTACTAGTGCTATCA[A/G]TTTTACCTCTAAAAT | 7525 |
rs545408473 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:725258 | TTTCCAAATTCTTCC[C/T]GATAGTGTCTCACTA | 7525 |
rs545411798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:783107 | ATTATATAGCCACTA[A/G]GTTTGGTGGCACATG | 7525 |
rs545442339 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:754497 | ACATCCCCTAAATCA[G/T]GAGTTTAAGACCAGC | 7525 |
rs545442479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:806065 | TACACCTATGAATTA[C/T]GCATTCCTTCACACA | 7525 |
rs545468322 | snp | A/C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723047 | CAGTGAGCCGAGATC[A/C/G]CGCCACTGCACTCCA | 7525 |
rs545502265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:791803 | CTCACGTCTGTAATC[C/T]CAGCACTTTGGGAGG | 7525 |
rs545506868 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:780077 | TGTCTCTACTAAAAA[A/T]ACAAAAATTAGCCAG | 7525 |
rs545514481 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:779344 | GGGAGGTCAAGGCTG[A/C]GGTAAGTTATGATCG | 7525 |
rs545568414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:794575 | TAGAAAAAAAATGGC[C/T]TAAAATAACAAATTT | 7525 |
rs545580807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:733509 | TGGCTTTCGGCCGGG[C/T]GCGGTGGCTCAAGCC | 7525 |
rs545584485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776467 | TTACATATGTTTACC[A/G]GACATTATCTTTTGT | 7525 |
rs545616123 | in-del | -/TGAG | | | intron-variant | YES1 | GRCh38.p7 | 18:769628 | AGTTTTTATCATAAA[-/TGAG]TGAATTTTGTCAAAA | 7525 |
rs545712098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:780984 | CATAAAATAGAAGAC[C/T]TTGGCCAGGGGCGGT | 7525 |
rs545741183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:747566 | CCTCATATATAAGCT[A/G]TAAGTTAAAAAATAA | 7525 |
rs545766475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:804771 | ACACAAAAATTAGCC[A/G]GGTGTGGTGGCACAC | 7525 |
rs545780212 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:741539 | CTGGGTGTGGTGGCT[C/G]ACACCTGTAATCCCA | 7525 |
rs545808653 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:783761 | GCTGGGATTACAGGC[A/G]CTGCCACCATGCCCA | 7525 |
rs545829440 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:725334 | TCCCTGCCTGCAAGT[C/T]AGGCCATCCCTTGTA | 7525 |
rs545858890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:771265 | CCAGCTACCTGGGAA[A/G]CTGAGGCATGAGACT | 7525 |
rs545894957 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:807245 | AGGCTGAGGCAGGAG[A/G]ATCACTTGAACCTGG | 7525 |
rs545897187 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:803658 | TTATTGGGAGAATCT[C/G]AGTCTCCTAACAGGG | 7525 |
rs545917060 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:759555 | GCATCCATGGATTCA[A/G]CCAAGATTCAAAAGT | 7525 |
rs545985337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:770873 | GAAAAGTTGCCAGAG[C/T]GGTGGCTCATGCCTT | 7525 |
rs545992785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:811086 | AATATTTAAAATTAT[C/T]AAGGTATCTTTGGCA | 7525 |
rs546018297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:742295 | CATCTTGTGGTCTAG[A/G]GTTAAGGAAAATGAA | 7525 |
rs546039917 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:793190 | GACTACAGGCGCATG[A/C]CACCATGCCCGGATG | 7525 |
rs546040993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:740957 | GGCTGGAGTGCAGCG[A/G]TGTCATCTTGGCTCA | 7525 |
rs546045181 | in-del | -/GCG | 0.496045 | 0.0442933 | intron-variant | YES1 | GRCh38.p7 | 18:812023 | CGGGGAACCGCGGCG[-/GCG]GCGGCGGCGGCGGCT | 7525 |
rs546058594 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:735505 | AGGGGGAAAGGTTGG[G/T]GGGTGGATAAAAGAC | 7525 |
rs546062377 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:732569 | GTAAGAGGCCCCTTT[A/G]GAAAATGTCCTGAGA | 7525 |
rs546073764 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:798777 | GGGGTACACTGTCCA[A/T]TAGAATTTTAAGCCT | 7525 |
rs546095528 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:785170 | TTTTTTTTTTTTAAC[A/C]TCATCAGCTATTGTT | 7525 |
rs546095687 | in-del | -/ACAAC | | | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721559 | AAACAAAACAAAACA[-/ACAAC]AAAAAAAAAGAAAAT | 7525 |
rs546131992 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:731706 | GGCACGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 7525 |
rs546136052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:799340 | TCCAGCTCTCCTTAC[A/G]CTCAGATAAATCCAT | 7525 |
rs546160181 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:800919 | TTGGGAGGCCAAGGC[A/G]GGTGGATCACGAGGT | 7525 |
rs546201637 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:753195 | TCTTTTAAAAAACTG[C/T]ATATATTTATTGCAT | 7525 |
rs546246612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:764757 | CTTTTTTTTGAGACG[A/G]AGTCTCGTTCTGTCA | 7525 |
rs546250307 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:794214 | GCGTGCCTCCTGATG[G/T]CTTGTACTCTGAAGA | 7525 |
rs546288157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:806464 | ATTAAGCTAGTTTTA[C/T]AACATTTTAGTAGAG | 7525 |
rs546290951 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:750281 | TTCATTGATTCACTC[C/T]AACATTTACTGAATA | 7525 |
rs546293592 | snp | C/T | 1.73168e-05 | 0.00294246 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724406 | GCAGATTTGTGCATA[C/T]AAAATAGGCTACTTG | 7525 |
rs546296473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:807144 | GCATGCTCCAGTCTG[A/G]CCAACATGGTGAAAC | 7525 |
rs546296879 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:730765 | TTTACAGTGCTATAA[G/T]AAGTTGGATATTAGC | 7525 |
rs546300226 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:800393 | AGCCATTCCAGTCAT[C/T]TGGAGTTGGTACAAC | 7525 |
rs546302259 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:721938 | AAAGCTGTTGGAAAA[C/T]ATCTCCAAATTTACA | 7525 |
rs546399391 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:733200 | ATAAGTTGGCTGTGG[A/G]AACAGAAAACAATTT | 7525 |
rs546430446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:760091 | ATATGTGCCACATTT[C/T]CTTAATCCAGTCTAT | 7525 |
rs546432342 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:788158 | ATAATGAAGTAAAAA[A/C]ATTAATATGGAAATA | 7525 |
rs546472498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:755242 | GTATGGCAGTCCTCT[A/G]GCCATTGCCTTTTTT | 7525 |
rs546488108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:748522 | AAAGAAACTCTGTAC[C/T]CATTAGCAGTCACTC | 7525 |
rs546496350 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:783251 | AACATTATACTGCAT[A/T]TTTTAGCTACAGACC | 7525 |
rs546502104 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721186 | TAACTGTATTTGCTG[G/T]TATAATTTTAAGAAG | 7525 |
rs546522825 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:792624 | ACATACATATATATA[C/T]GCACACACATTCATA | 7525 |
rs546533986 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:755910 | TTTTAAAATTGTTTG[A/C]ATCTATTTTTTTAAG | 7525 |
rs546583513 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:755098 | ACTCTAAAAGTAAAC[G/T]TTTGCTAAAGACTTA | 7525 |
rs546615691 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:762013 | CCAATGTGGAGAAAC[C/G]CTGTCTCTACTAAAA | 7525 |
rs546629699 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:757277 | GGGAGGCCAAGGCGG[A/G]CGGATCACGAGGTCA | 7525 |
rs546651984 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:733285 | TAACTTTTAAGTACA[C/G]TCTGGCACCTAATAG | 7525 |
rs546652094 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:738909 | GCTCACTCCAACCTC[C/T]GCCTCCCGGGTTCAA | 7525 |
rs546688907 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:733644 | AAAAATTAGCTGGGC[A/G]AGGTGGCAGGAGCCT | 7525 |
rs546738253 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:781764 | TAAGACTGAATTTCC[-/T]TTTTTTTTTTGGAGG | 7525 |
rs546768087 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:757435 | GTGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 7525 |
rs546833663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:781182 | GCTGAGGCAGAAGAA[C/T]TGCTTGAACCTGGGA | 7525 |
rs546835687 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:773430 | TAAAACAGCCCCTTT[A/C]CTATTTCTTATATGG | 7525 |
rs546942997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:763497 | CCTAGAAATTTGAGA[A/G]CAGCCTGGGCGTCAT | 7525 |
rs546953831 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:767739 | CAGAGTCTCGCTCTG[C/T]GCCTAGGCTGGAGTA | 7525 |
rs546955732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:800270 | CTGCATGTTCCTACA[A/G]TCAAAAATATTTAAT | 7525 |
rs546975272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:762914 | GACAAAATGTTAGAG[C/T]GGAGGTATGTACAAA | 7525 |
rs547010953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:764818 | ACTCACTGTAACCTC[C/T]GCCTCCTGGGTTCAT | 7525 |
rs547012513 | in-del | -/AT | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:768578 | CTCTTCATCACTAAC[-/AT]ATACCATCATGTGCA | 7525 |
rs547053171 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:807956 | TCACAGCTTACTGTA[A/C]ATTTGAACAAGAGAA | 7525 |
rs547074494 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:761824 | ACTAATGTCATACGT[C/G]ATTCACATTTTTAAG | 7525 |
rs547094113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:735607 | TAATCCCAGCTACTC[A/G]GGAGGCTGGGGCAGG | 7525 |
rs547094848 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813906 | GATCACTTGAGTCTA[A/G]GAGTTGGAGACCAGC | 7525 |
rs547109727 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | YES1 | GRCh38.p7 | 18:764077 | GTGAGCCGAGATCAC[A/G]CCACTGCACTCCAGC | 7525 |
rs547119840 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | YES1 | GRCh38.p7 | 18:794721 | CTGGCAATCCTTCGT[A/G]CTCCTGGCTTACAGG | 7525 |
rs547120164 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:792262 | TGAGCTGAGATTGTG[C/T]CACTGTACTCCAGCC | 7525 |
rs547120793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:730950 | TGATGAAATCAGAGA[A/G]GGGTGAAATCAGCAA | 7525 |
rs547183103 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:790269 | TAACTCCAGCTACTT[C/G]GGAGGCTGAGGCAGG | 7525 |
rs547187822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:759793 | TATACATGTGCCATG[C/T]TGGTGTGCTGCACCC | 7525 |
rs547246402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:799045 | CTGCTTTAAGAAACA[C/T]ATTTCTTAAATGTGT | 7525 |
rs547247955 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722867 | GGAGGCCGAGGCGGG[C/T]AGATCACAAGGTCAG | 7525 |
rs547284397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:755398 | GGACTACAGGTGCGC[A/G]ACACCACACCTGGCT | 7525 |
rs547308963 | snp | A/G | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:814223 | CCTGGAAAGTTTTCA[A/G]TCTTACATTTAGTGG | 7525 |
rs547321618 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:765019 | GATTACAGGCGTGAG[C/T]CACCTCGCCCGGCTT | 7525 |
rs547321967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:759370 | TACTTGGGAGGCTGG[C/T]GCAGGAGAATTGCTT | 7525 |
rs547355725 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:724894 | AAGCCAACCCCATTT[C/G]ATTAATAAGAATTTA | 7525 |
rs547391749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:771341 | CACTACACTACAGCC[C/T]GGGGAATAAGAGCAA | 7525 |
rs547405664 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:778593 | GGAATAGCCCTAGTC[G/T]GGCATTTTGCCCAGA | 7525 |
rs547460372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:756176 | CATCTATTAAGTAAC[C/T]ACTATAAGACTTTAA | 7525 |
rs547473460 | snp | A/G | 0.00835141 | 0.0640778 | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721261 | ATTGACCACAGGCCG[A/G]GCGCGGTGGCTCACG | 7525 |
rs547500172 | snp | A/C | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813406 | AGAGTAACTTCCTCT[A/C]TTTATTTCCTCTTTG | 7525 |
rs547527137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:784868 | TACCTGCAACTGTAA[C/T]TCCTCTTTACCATGT | 7525 |
rs547623875 | snp | C/G | 0.000798403 | 0.0199641 | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721432 | AGTCCCAGCTACTCG[C/G]GTGGCCGAGGCAGGA | 7525 |
rs547667209 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:784569 | TCCCTGGACTAAAAT[C/T]AAGGTGTCAGCAGGG | 7525 |
rs547667738 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:765800 | CAAGTCAAGTGGCAC[G/T]TAAAATGATTTTTTT | 7525 |
rs547709094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:804389 | AAGGCAGGCAGATCA[C/T]CTGAGGTCAGGAGTT | 7525 |
rs547713764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:779345 | GGAGGTCAAGGCTGC[A/G]GTAAGTTATGATCGC | 7525 |
rs547714541 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:726428 | GGACTCCATCTCAAA[A/G]ACACAAAAACAAAAA | 7525 |
rs547765901 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:744678 | TACAGGAGTGAGCCA[C/T]CACGCCTGGCCTTTT | 7525 |
rs547798212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:742864 | ATATGCATACAAATC[A/G]AGACTCTTAAAAACA | 7525 |
rs547803191 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:772202 | ATCCAGCTAATTTTG[C/T]ATTTTCAGTACAGAC | 7525 |
rs547851548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:799517 | GAGTTTGAGGCCAGC[C/T]TGACCAACATGGTGA | 7525 |
rs547860244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:743646 | GGCAAGGTGTCTCAC[A/G]TCTGTAATCCCAGCA | 7525 |
rs547877203 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:746413 | GTGGTTCCCTGGTAA[A/C]AGCATCATCATCTGC | 7525 |
rs547886723 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723058 | GATCGCGCCACTGCA[C/G]TCCAGCCTGGGCGAC | 7525 |
rs547964659 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:727360 | ATACCTTAAAGTATG[C/T]ATCTTATAAATACCA | 7525 |
rs547972558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:766446 | AAGGGATAGCACTAC[A/G]TGATTAGTGAAAGAT | 7525 |
rs547972720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:802111 | CATTAAAAAGAAAAG[C/T]CTAGGGTGGGTGTAG | 7525 |
rs548000892 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:746602 | AAGCACCATAGTAGA[A/T]CAAAGAGTTATTGAG | 7525 |
rs548062340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:781905 | CAAGGACAGAATCTG[A/G]CTAGAGGTAGCTTAA | 7525 |
rs548097666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:759185 | TCAAAATATAACCGG[A/G]GCTAGGCGCGGTGGC | 7525 |
rs548112722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:737527 | TGTGTCTGTGGTTAG[A/G]AGAAGAGGTAAATCA | 7525 |
rs548124321 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:782361 | CCAGCTTGGATCAGC[C/T]GCCTCCCTCTGGGTC | 7525 |
rs548132166 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723264 | TAGTTTTATAGTTAT[A/G]CTTTATAACTCTTCA | 7525 |
rs548142418 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:786145 | ACACAAAATAAACTA[A/C]GAAACCCTAAGATGC | 7525 |
rs548161768 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | YES1 | GRCh38.p7 | 18:744547 | GGTGCATGCCACCAC[A/G]CCTGGCTAAATTTTT | 7525 |
rs548192866 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:745477 | ATGTAAATACTATGC[A/C]AGTAAGATATAAGGA | 7525 |
rs548226378 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:803671 | CTGAGTCTCCTAACA[A/G]GGAACTCAAAACAGT | 7525 |
rs548238679 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | YES1 | GRCh38.p7 | 18:751785 | ATAATCATATAAGGC[C/T]ACAAATATAGTAACA | 7525 |
rs548253335 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:783653 | CAGAGTTTCACTCCT[A/G]TTGCCCAGGCTGGAG | 7525 |
rs548260385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:803737 | AGGAGGGTGACTGGC[A/G]AGGCTACAGGTTCAC | 7525 |
rs548261100 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:795622 | GACATGGATGAAGCT[C/G]GAAATCATCATCCTC | 7525 |
rs548273254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:809165 | TTACAACATACAAGC[C/T]GAAGCGGATTTTAAT | 7525 |
rs548285627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:809696 | AGCCTAGGTAGTGTT[C/T]GAAAGTCAGCCACCA | 7525 |
rs548308142 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:749813 | TGCAGTGAGCCGAGA[C/T]TGCGCCACTGCACTC | 7525 |
rs548308206 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:779493 | CTTACAAATTAAAGC[C/T]TCAAGATTTTTAAAA | 7525 |
rs548324675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:768789 | CTCACTGCAACCTCC[A/G]CTTCCCAGGTTCAAG | 7525 |
rs548372002 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:729554 | TTCCATATATTGCTA[G/T]TTTGAAGTCTTTTGC | 7525 |
rs548402917 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:741124 | GCTGGGATCGAACTC[C/T]TGACCTCAAGTGATC | 7525 |
rs548463241 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:805342 | TGTAGAAGAGATACA[A/G]TAATTACACAGTATA | 7525 |
rs548469390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:734270 | GGCAAAAAAGCAAAA[C/T]TTGGCCAGGCGCGGT | 7525 |
rs548508417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:740221 | GTCGCTGTGGAACTA[C/T]TGCTGTGACCAAGCT | 7525 |
rs548573458 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:754149 | TTCAATCAAATCCTT[C/T]ACTTAATCTCTTCAG | 7525 |
rs548583422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:797562 | ACAAGAAAGTACCAC[C/T]GACAATGACCTATAT | 7525 |
rs548683206 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:797370 | AGAGCTTTAAACCTG[C/T]TAACATCCCTGGCTC | 7525 |
rs548689945 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:726348 | GAGAATCGCTTGAAC[C/T]TGGGAGGTGGAGGTT | 7525 |
rs548708573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:756347 | TGACATGATCCAGTA[C/T]ATAATCACCATCAGG | 7525 |
rs548733985 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:799728 | TTAATTTAAAAATAA[A/G]AAACACAAATACAAA | 7525 |
rs548737117 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:763947 | TAACAGGGCGAAAAC[A/C]CGTTTCTACAAAAAA | 7525 |
rs548755624 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:783398 | TAGGGGAAACACACA[C/T]ACACACACACACACG | 7525 |
rs548768084 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:791979 | TTTACACTTACAGTA[A/C]ATCTCAATTTGGACT | 7525 |
rs548781268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776195 | ATACTTGGTATACTC[A/G]ATCTTTTTTTTTTTT | 7525 |
rs548810007 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:747728 | GACTGATGCAGATTC[A/G]TTTATGATCCTACTC | 7525 |
rs548810675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:744377 | AAGTTCATTTAGGAT[C/T]ATTTAGGAGATTTTT | 7525 |
rs548820655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:806056 | CAGCAAAAGTACACC[C/T]ATGAATTATGCATTC | 7525 |
rs548860115 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:721869 | TAGAAGGCTGTTTTT[C/G]CCAACTTCCTTTTTT | 7525 |
rs548930971 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:734848 | CAGCAAACCCACTAC[G/T]GGGTATCTTCCCAAA | 7525 |
rs548943747 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:791261 | AAGAAGAAAAAAAAA[A/G]GAAAAAAAAAAAAGA | 7525 |
rs548984980 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:767216 | GTACAGTGACATGAT[A/C]ATGGGTCACTGAAAC | 7525 |
rs548993881 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:806437 | AGAATTAACTTCGAG[C/T]TATGAAAAAGTATTA | 7525 |
rs548997073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:766348 | TCATCGATGATGCCT[A/G]GATCAAATGACTTGC | 7525 |
rs549007328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:761341 | AATATCAAGAAAACA[A/G]CATTAATTATTACAT | 7525 |
rs549044833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:731851 | GGGTGCCTATAGTCC[C/T]AGCTACTCGGGAGGC | 7525 |
rs549060842 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:729044 | GTTACTGTTTCATTT[C/T]TTTCTCTCTTCTGCT | 7525 |
rs549132833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:773855 | TTTTTTTTTTGAGAC[A/G]GAATCTTGCTCTGTC | 7525 |
rs549143491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:750097 | AAAGGCACTGTCTAA[A/G]TTAAAATGTTATAAA | 7525 |
rs549159053 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:762855 | AAGGTCACAAATGTA[A/T]GAAACAAATACAACA | 7525 |
rs549164676 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:794719 | AGCTGGCAATCCTTC[C/G]TGCTCCTGGCTTACA | 7525 |
rs549303377 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:794046 | GCAATAATTAATTCA[A/G]CCAAGGAATCATCAA | 7525 |
rs549303827 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:767687 | AATTATATAATATAA[A/T]GCCTCCAGTTTTTTC | 7525 |
rs549303855 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:762169 | CTACTAAAAATACAA[A/C]ATTAGCTGGGCGTGG | 7525 |
rs549317213 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:773321 | TCCCTCCTCATACCT[C/G]AACTACTTTCATCTT | 7525 |
rs549325912 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:741407 | ACCACGTCCTGCTAA[-/T]TTTTTTTAGTTTTTG | 7525 |
rs549365568 | in-del | -/G | 0.0220376 | 0.102631 | intron-variant | YES1 | GRCh38.p7 | 18:792861 | TCAATAAAAGCCAAG[-/G]GGGGGGGAAAAAGCT | 7525 |
rs549394480 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:733548 | CAGCATTTTGGGAGG[C/T]CGAGGTGAGTGGATC | 7525 |
rs549419947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:747262 | ATCACTTGAGGTCAG[A/G]AGTTTGAGACCAGCC | 7525 |
rs549432702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:728371 | ACCTTATACATATAG[C/T]CTGAAGGTAATTTTA | 7525 |
rs549471521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776166 | ATGAGAATTACCATT[A/G]CTTTACATCATCAAT | 7525 |
rs549482380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:787261 | CCCACCACCAAGCCC[A/G]GCTAATTTTTGTATT | 7525 |
rs549489703 | in-del | -/AT | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:725147 | TTCAAGATATTACAC[-/AT]AGTTCCTTTCTTGTA | 7525 |
rs549558075 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722859 | GCACTTTGGGAGGCC[A/G]AGGCGGGCAGATCAC | 7525 |
rs549563059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:764768 | GACGGAGTCTCGTTC[C/T]GTCACCCAGGCTGGA | 7525 |
rs549610546 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:771028 | AAAAAAAATCTGAAA[A/T]GTTAAAACCTAGAAA | 7525 |
rs549618730 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:741087 | ATTTTTAGCAGAGAC[A/G]GGGTTTCGCTATGTT | 7525 |
rs549622651 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:800421 | AACAGCAGTTCGAAA[C/G]CTATCTGCCAACCTT | 7525 |
rs549651883 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813841 | TAAAATAGGCCGGGC[A/G]CAGTGGCTCACACGT | 7525 |
rs549662930 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:790448 | TTCTGTTTCTCGTTT[C/T]TAATTCATTACCTTT | 7525 |
rs549694866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:807405 | TCAGGAGGCTAAAGT[A/G]GGAGGATCCCTTGGG | 7525 |
rs549696578 | snp | A/G | 0.0123036 | 0.0774623 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722956 | AACTAGCCAGGCGTG[A/G]TGGTGGGCACCTGTA | 7525 |
rs549715294 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:807876 | TAAACAACAATAAAA[C/G]AAGCAATTCTAAGAA | 7525 |
rs549718932 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:759339 | GGGCGAGGTGGCGGG[C/T]GCCTGTAATTCCAGC | 7525 |
rs549772935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776561 | TTGTAAGGCATTCTT[C/T]AATTTTCTGTGTATT | 7525 |
rs549855685 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:798327 | ATCATCAATATTGTT[G/T]TTCCTTTTCTGAAAC | 7525 |
rs549860367 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:805759 | AATCACATCAGAACA[A/G]AAGTTAGAAGTCAAT | 7525 |
rs549873202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:735893 | TAAAGATTACAGGCC[A/G]GGCATGGTGTCTCAC | 7525 |
rs549976997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:754799 | CCTTCACCATCATTC[C/T]AGTTAGTTCCTTCAT | 7525 |
rs550031795 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:735533 | GACTACATGTTGGAG[A/G]TGAAACCCCGTCTCT | 7525 |
rs550108857 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:785363 | AACAAGTCAATAAGA[C/G]ATATCATCTTCCCCT | 7525 |
rs550123270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:795506 | CTTGGAACCAACCCA[C/T]ATCCCCATCAATGAT | 7525 |
rs550127922 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:755321 | TGGCGCAATCTTGGC[C/T]CACTGCAATCTCTGC | 7525 |
rs550214420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:736000 | ACATGGCAAAACTTC[A/G]TCTCTACAAAAAATA | 7525 |
rs550215449 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:759663 | CAATAACTATTTACA[C/T]TGTATTAGGTATTAT | 7525 |
rs550237963 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:804877 | TGAGATCAAGCCACT[A/G]CACTCCAGCCTGGGC | 7525 |
rs550249725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:800975 | ACTTGGTGAAACTCC[A/G]TCTCTACTAAAAATA | 7525 |
rs550255522 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:777720 | GCTGAGGCAGGAGCA[C/T]TGCTCTAACCCAGGA | 7525 |
rs550262247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:794950 | CCTCCCAAGTTGCTC[A/G]AACTACAGGCGCGTG | 7525 |
rs550280162 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:787414 | ATACATACTGTATTT[A/T]AAAAAATTTGTTGGG | 7525 |
rs550347012 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:745053 | TTGCTGGCTGACTTG[A/G]TAGACTCAGTTTGCA | 7525 |
rs550358752 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:771450 | TATTATAACAGATAA[A/C]ATATTTATTCCTTAA | 7525 |
rs550394545 | snp | G/T | 5.18247e-05 | 0.00509015 | intron-variant | YES1 | GRCh38.p7 | 18:736757 | GTATAGTCAAGAGAG[G/T]TAAGCAAAACACACA | 7525 |
rs550438943 | snp | A/G | 0.00478085 | 0.0486577 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722838 | TGGCTCACGCCTGTA[A/G]TCCCAGCACTTTGGG | 7525 |
rs550453477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:781814 | GGTTGTAAGAATTAA[C/T]TGATATCATATGCAA | 7525 |
rs550513084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:743527 | AACAGAAGTCCTTTC[A/G]AGTTTTACTCTAAAA | 7525 |
rs550522453 | snp | C/T | 0.00597247 | 0.0543191 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722919 | AACACGGTGAAACTG[C/T]GTCTCTACTAAAAAT | 7525 |
rs550524023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:729450 | ATAAATACAATTTCC[A/G]TTTGATTCTTTTTTT | 7525 |
rs550574296 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:751293 | AACTTAATTTCATCA[A/G]TTGGAAAGTAGATGG | 7525 |
rs550593689 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:733550 | GCATTTTGGGAGGCC[A/G]AGGTGAGTGGATCAT | 7525 |
rs550610678 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:777261 | CTTCTATTTAGCACT[A/G]ATTGTTTTATATATG | 7525 |
rs550648165 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722606 | CCACTAATGCTGCTA[C/T]TCAAATCTGTATTTT | 7525 |
rs550651382 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:789299 | TATAAAAGAACAACT[C/G/T]TGCGAGGCATGGTGA | 7525 |
rs550656438 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | YES1 | GRCh38.p7 | 18:731827 | AAAAAATTAGCTGGG[C/T]GTGGTGGCGGGTGCC | 7525 |
rs550684824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:729021 | AGCCATTACTTTTTA[A/G]AAATGTTGTTACTGT | 7525 |
rs550719602 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:729760 | GCCTCCCGAGTAGCT[A/G]GGATTACAGGCGCCC | 7525 |
rs550719664 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:757094 | ACATGCCACAGTATA[C/T]TGGGAAAAAACCATG | 7525 |
rs550724036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:809043 | TGCCGTAATTGAGTT[C/T]TGAGTTTTAATTGTC | 7525 |
rs550738309 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:760402 | TTGAATCTGGGAGGC[A/G]GAGGTTGCAGTAAGT | 7525 |
rs550783116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:734207 | TTGCTTGAACCTGGG[A/G]GGCAGAGGTTGCAGT | 7525 |
rs550798469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:733962 | CAATTTTCCTTGGCA[C/T]CATTACAAAATGTTT | 7525 |
rs550802453 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:754029 | TGTCATTTCTCACAG[G/T]GACTGGGTGGACTAC | 7525 |
rs550809389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:774599 | CCTCAGTAACCCCCC[A/G]GCCCTATTCTCAAAA | 7525 |
rs550829331 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:754521 | GACCAGCCTGGCCAA[C/T]GTGGTGAAACCCCGT | 7525 |
rs550839866 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:788291 | CATGGGGAGCCTTTT[A/G]GCGTGGGCTATAAAA | 7525 |
rs550847716 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:745417 | CCCATAAATATTTGC[A/T]TTTAGGTTTATTTTC | 7525 |
rs550861448 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723028 | ACCTGGGAGGCAGAG[C/T]TTGCAGTGAGCCGAG | 7525 |
rs550905685 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:801899 | TGGCGGAACAAACAC[C/T]TTATTTTATAAAAAG | 7525 |
rs550910856 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:746165 | AAGAATAGCTAGAGA[A/C]CATGGCTCAAAATAC | 7525 |
rs550922125 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:763053 | GGGGGAAAGAAAAGG[A/C]TATTCCAGGAAGAAT | 7525 |
rs550938269 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:790201 | GCCAACATGGTGAAA[C/T]CCTGTCTCTACTAAA | 7525 |
rs550956613 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:757465 | CAGAGATCGCGCCAC[C/T]GCACTCCAGCCTGGG | 7525 |
rs550958971 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:757869 | GATAAAATTATCTGT[C/T]AAAAAAAAAAGAAAA | 7525 |
rs550982827 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:769209 | ATCGCCTGATGACAC[A/T]ATGTCAGAACATATT | 7525 |
rs551045737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:730971 | AAATCAGCAAAGGAG[C/T]GATTATACTGCTTCA | 7525 |
rs551047583 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:735908 | GGGCATGGTGTCTCA[C/G]GCCTGCCATTTTAGC | 7525 |
rs551049228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:725597 | ACTGTCATCTTCATA[A/G]GTGAAATCTGGCCGG | 7525 |
rs551077889 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:765055 | AATCTTTTAAAGATA[A/C]CAGAACTCTCAAATA | 7525 |
rs551096124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:759840 | CATTAGGTATATCTC[C/T]TAATGCTATCCTTCC | 7525 |
rs551123438 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:768770 | TGCAGTGGTGTGATC[C/T]CGGCTCACTGCAACC | 7525 |
rs551137598 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:756270 | TAATCTTTATGTTCC[C/T]GGTGCCTACAGTGGG | 7525 |
rs551148421 | snp | C/T | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812436 | ACGCCGGCCCGGCTC[C/T]GGGGCCCCCAGCCTT | 7525 |
rs551158490 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:797354 | CTGGGAAAATATAGA[A/T]AGAGCTTTAAACCTG | 7525 |
rs551201469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:749630 | GGAGACCGAGGCAGG[C/T]GGATCACAAGGTCAG | 7525 |
rs551202564 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:811374 | AAGTCCCTACACCAG[A/C]CTTGATTTTCAAAGA | 7525 |
rs551229901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:755484 | CTCAAACTCCTGAGC[C/T]CAGGCAATCTGCCTG | 7525 |
rs551250342 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:727223 | ACCCTTTTATTATTA[C/T]GAAACGTCCCTTTTT | 7525 |
rs551261686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:793384 | CTCTGTCACCCAGGC[C/T]ACAGTGCAGTGGCAT | 7525 |
rs551287694 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:810966 | TGATAGTTAAGATAT[C/T]AGATTTACCATGCAC | 7525 |
rs551294091 | in-del | -/TT/TTT | 0.442113 | 0.159977 | intron-variant | YES1 | GRCh38.p7 | 18:769957 | ATTCTCTTCCTGTTC[-/TT/TTT]TTTTTTTTTTTTTGA | 7525 |
rs551332657 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:778842 | AAGCAGCAGACTACT[-/A]AAGGGCATACACTTT | 7525 |
rs551356387 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:765634 | CGAACGCCTGACCTT[A/G]TGACCCACCCACCCT | 7525 |
rs551374275 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:772362 | TGCAGGTCTTGATAC[C/T]AGGTAAACATTGCTT | 7525 |
rs551384722 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:811755 | TCCCTCGCCCCTACT[G/T]CGGCCGTAGGGGCAA | 7525 |
rs551387184 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:729223 | CCCATCTAGTGAGTA[C/T]TTAATTTGATATAAT | 7525 |
rs551496420 | in-del | -/ATATTA | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:753170 | TAAAAACTCCATAAT[-/ATATTA]ATATTCTTTTAAAAA | 7525 |
rs551537574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:743736 | TACAGTGAAACACTG[C/T]CTCTACTAAAAATAC | 7525 |
rs551548060 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:767165 | TACATTCAAAAAAAA[A/C/T]TTTTTTTGAGACAAG | 7525 |
rs551621757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:760384 | CTGAGGCAGAAGAAT[C/T]GCTTGAATCTGGGAG | 7525 |
rs551644008 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722077 | CATTCAGTTAAAACC[C/T]AATGAATACCATCAA | 7525 |
rs551650638 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:726285 | AAAAAATTAGCTGGG[C/T]GTGGTGGTGGGCATC | 7525 |
rs551669877 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721319 | GAAGCGGACGGATCA[C/T]GAGGTCAGGAGATCG | 7525 |
rs551674595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:761626 | AGTCTTCCATTACTA[C/T]GCTTAACCTGTCCTC | 7525 |
rs551685650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:773274 | CATTACCAGAGGGAG[A/G]AGTCAGGTCAGTACA | 7525 |
rs551709073 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:782424 | TGGAACATGGCAGAT[C/G]CCACCTGAACCATGA | 7525 |
rs551710556 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:799628 | CAGGAGAATCCACCT[C/G]GGAGGTGGAGGTAGC | 7525 |
rs551799812 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:806555 | GCCCAGAACCACATC[C/G]CTACATACAATTCAG | 7525 |
rs551806960 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:753491 | TCAGATCAAAAAAAA[A/T]TTTTTTCTTTTTTGA | 7525 |
rs551814184 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:766480 | TATCTTTTCTATGTT[C/T]TCGTATTTATGGAAG | 7525 |
rs551867320 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:744231 | GATGGGATTCAAATC[C/T]AGGTCTGTCTGCTTC | 7525 |
rs551872214 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:744151 | CACAAGTATCTCATA[C/T]ATAAATGAAGCTTTG | 7525 |
rs551889673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:786017 | ATAACACAGCAAGAA[A/G]AAGGCCCTTGCCAGA | 7525 |
rs551892230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:781980 | AATTCAGGGTCATAA[A/G]AGAAACTAGAACCAG | 7525 |
rs551936026 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:740335 | AAGGCTTATAATCAA[C/G]AGAAAACATCACACA | 7525 |
rs551956902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:762095 | GGAGGCCAGGGTGGG[C/T]GGATCACCTGAGATT | 7525 |
rs551970961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:796682 | AGAATCACTTGAACC[C/T]GGGAGGTGGAGGTTA | 7525 |
rs551977727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:807195 | AAAAATTAGCCGGGC[A/G]TGGTGGTGCACGCTT | 7525 |
rs551981343 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:747265 | ACTTGAGGTCAGGAG[C/T]TTGAGACCAGCCTGG | 7525 |
rs551993444 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:773262 | TAAGTCACCTGCCAT[C/T]ACCAGAGGGAGGAGT | 7525 |
rs551994584 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:738771 | CCTCATCCATTTTAA[C/T]TTTCTTAAAATTATC | 7525 |
rs552026221 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:790308 | TTGAACCCGAGAGGC[G/T]GAAGTTGCAATGAGC | 7525 |
rs552065429 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813073 | CGACTATCCCAGTCA[C/T]GGTGGCTTTGGCTTA | 7525 |
rs552087485 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:764291 | ACAATGGTACAATCC[C/T]GGCACACTACAACCT | 7525 |
rs552105932 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:771006 | AGATATCCCATCTCA[-/A]AAAAAAAAAAAAAAT | 7525 |
rs552110304 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:809988 | TGCTTCTATTTTTAC[G/T]TTCACAGAATTTCCT | 7525 |
rs552120537 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:781127 | ACAAAAAATTAACTG[A/G]GAGTGGTGGCAGGCA | 7525 |
rs552122089 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:809843 | GGCTTAATGAATTAC[A/T]CTAAGACCAATACCC | 7525 |
rs552125597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:733075 | ACTGTAGTCATCAGT[A/G]TCAATTCTTTAAATG | 7525 |
rs552126965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:798265 | TTCAAGTTTCCTGAA[C/T]TACAGATTCATGACT | 7525 |
rs552184480 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:749773 | GCTTAGGCAGGAGAA[C/T]GGCATGAACCCAGGG | 7525 |
rs552227399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:789564 | CTTCAGCCTAGGCAA[A/G]AGAGCAAGACTCTGT | 7525 |
rs552237768 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:786846 | ATTTTAATATATATA[C/T]GGCATCTTTGAACAG | 7525 |
rs552244026 | snp | C/T | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775805 | TTGCCTCAAATAAAT[C/T]AAAAAAAAAAATAGA | 7525 |
rs552263512 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:804251 | TAGCCACGATTACTT[G/T]TTAACTGACATCATA | 7525 |
rs552282599 | in-del | -/TGTG | 0.154456 | 0.231022 | intron-variant | YES1 | GRCh38.p7 | 18:792570 | CCCTCTGTATATGTG[-/TGTG]TGTGTGTGTGTGTAT | 7525 |
rs552389307 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723046 | GCAGTGAGCCGAGAT[C/T]GCGCCACTGCACTCC | 7525 |
rs552440743 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:730371 | TTTTTTTGAGACAGG[C/G]TCTTGCTCTGTTGCC | 7525 |
rs552463644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:734721 | TGTTGGTGTGGATGT[A/G]GTGAAAAGGGAACAT | 7525 |
rs552467236 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:809287 | AAATTCTCTAATTAT[C/T]GTACATTTCGGAGTA | 7525 |
rs552472642 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:726880 | ACCTGTTAGCATTTA[C/T]CAAGGTTTATTACTA | 7525 |
rs552475327 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:769288 | ATATTTGTATATTAC[G/T]TTCTTGTGACTGTAC | 7525 |
rs552481732 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:800706 | CAAATAAAATTTCCA[C/T]TGGTAGCTTCTGATG | 7525 |
rs552502215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:734929 | TTGGGAAGCCAAGGC[A/G]TGTGGATCACCTGAG | 7525 |
rs552502280 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:729688 | CCAGAGTGCAGCGGC[A/G]CAATCTCAGCTCACT | 7525 |
rs552518210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:791393 | ATGTGCTAAATACTA[C/T]CCTAAGTACTCTTGT | 7525 |
rs552545782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:747863 | TGGCTAAGTAGAATG[C/T]GCATTAAAACATTTC | 7525 |
rs552580087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:747417 | GAGGTTGCAGTGAGC[C/T]GAGATCACGCCACTG | 7525 |
rs552580687 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:792021 | AAGTGCTCATCTATT[A/T]TACTGGAGAGTGTTC | 7525 |
rs552583373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:754268 | CCATATAATACAATT[C/T]TCCCCTCTGTTTATA | 7525 |
rs552635058 | snp | A/G | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:784005 | AAAATCCATTTCCTT[A/G]CATTAAGCAAAACAG | 7525 |
rs552659282 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:806702 | CAGTGCAAGGAGAGG[A/T]GTGTTTTGACATAAG | 7525 |
rs552666388 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:758634 | ACTTTTCCATTCAGG[C/G]TTTCCTTATAATCAG | 7525 |
rs552755897 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:749195 | ACAAAACAAAAACCC[A/C]AAAAAACTGCATTTC | 7525 |
rs552757025 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | YES1 | GRCh38.p7 | 18:794718 | TAGCTGGCAATCCTT[C/T]GTGCTCCTGGCTTAC | 7525 |
rs552758135 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776731 | AATTCTGCCTCATAA[C/T]CTGACAATATATGGT | 7525 |
rs552790758 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:793132 | GCAACCTCCACCTCC[C/T]GGGTTCAAGCGATAC | 7525 |
rs552817563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:771070 | CCCCGGTGTTAATAA[C/T]CATTCAAGTGATGGC | 7525 |
rs552819549 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:777578 | TTGGGAGGCTGAGGC[A/G]GGCGGATCACTTGAG | 7525 |
rs552859249 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:732195 | TGTAATCCCAGCACT[G/T]TGGGAGGCCTAGGCA | 7525 |
rs552910046 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:749712 | AAAAACAAAAAAAAT[C/T]AGCCAGACGTGGTGG | 7525 |
rs552937321 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:757240 | TGGGCGCAGTGGCTC[A/T]CGCCTGTAATCCCAG | 7525 |
rs552949657 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:757306 | CAGGAGATTGAGACC[A/G]TCCTGGCTAACACGG | 7525 |
rs552956826 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:782003 | AGAACCAGCAACCCA[C/T]GTTCTGGAAATTTGG | 7525 |
rs552966547 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:744507 | TGATTCTCCTGCCTC[A/T]GCCTCCCAAGTAGCT | 7525 |
rs552971300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:743836 | GCATGAACCCAGGAG[A/G]CAGAGGTTGCAGTGA | 7525 |
rs552976880 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:811048 | TGCGTAATTTAACTT[C/T]AGAAGTGTAACAGGA | 7525 |
rs553029919 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:772324 | ATGAGCCACCGCACC[C/T]GGCCTGCATGTTCAA | 7525 |
rs553069061 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:756427 | TTTATGTTAGAGACT[A/G]ATTTTCACATACAAT | 7525 |
rs553076252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:761804 | TCATCTCATTTTGAA[A/G]TATTACTAATGTCAT | 7525 |
rs553087905 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:773001 | ATAGGCTGGTCCTAT[A/G]GTTTCCTTAAGAGGC | 7525 |
rs553127063 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:751988 | CATGACCATATTTTA[C/T]GTTCTGGGACAATAA | 7525 |
rs553151315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:766734 | TTGGTGACGTGACTG[C/T]TCAAATCAGTTTTTA | 7525 |
rs553221709 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:767336 | TGTATTTTTTTGTAA[C/G]GACAGAGTTTCACTA | 7525 |
rs553281562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:779094 | GGATCAGCCATGAGA[A/G]GAGCCTGATGTAAAG | 7525 |
rs553308075 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:728103 | CACTTTGGGAGGACA[C/G]GGCAGGCAAATCGCT | 7525 |
rs553345240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:779872 | TTTAAACTTTAAAAA[C/T]ATCATCCACTTGTTT | 7525 |
rs553374639 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:758990 | TTCAAAAGGAAGTAG[C/G]TGAGTGTTGGCCGCC | 7525 |
rs553401981 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:795697 | ACTTATAAGTGGGAG[A/T]TGAACAATGAGAACA | 7525 |
rs553427887 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:764963 | CTAGTCTCAAACTCC[C/T]GACCTTGTGATCCGT | 7525 |
rs553440550 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:801061 | TGAGGCAGGAGAATC[A/G]CTTGAACCAAGGAGG | 7525 |
rs553478831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:764052 | ATGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 7525 |
rs553491157 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:793225 | TTTGTATTTTTAGTA[C/G]AGACAGGGTTTCACC | 7525 |
rs553500605 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:732656 | TTTCACTGACTTACC[A/C]GTCCAATGCCACAGT | 7525 |
rs553517543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:783668 | GTTGCCCAGGCTGGA[A/G]TGCAATGGTGCAATC | 7525 |
rs553526339 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:807477 | GCACTCCAGTCTGGG[A/C]AACAGAGCAAGATCC | 7525 |
rs553528380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:800747 | TCCAGTGATGTTCAT[A/G]TAACAGTAATAGTTA | 7525 |
rs553571272 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:766372 | GACTTGCTCCACATC[C/G]TTAAGACTTGTTATT | 7525 |
rs553596763 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:751422 | CTTTATAAAGTTTTT[A/T]AAAAAAATAATACAC | 7525 |
rs553610991 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | YES1 | GRCh38.p7 | 18:757322 | TCCTGGCTAACACGG[A/T]GAAACCCCGCCTCTA | 7525 |
rs553625053 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:759467 | ACGAAACTCCGTCTC[-/A]AAAAAACAAACAACA | 7525 |
rs553627288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:795037 | CCAGGATGGTCTCAA[C/T]CTACTGATCTCGTGA | 7525 |
rs553633531 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:751584 | CCAATGCATCGTTAA[A/G]CACAGTGGGCAGCCC | 7525 |
rs553637961 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:738656 | GATTGCACCACTGCA[C/T]TCCAGCCTGGGTGAC | 7525 |
rs553744043 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:784494 | CAAATTACCACAAAT[G/T]TAGTGGCTTAAAACA | 7525 |
rs553774006 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724087 | TAAATAATTTTCTTT[A/G]AGCAATTCTGACTTT | 7525 |
rs553777312 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:793860 | AATCTGAGCATCAAG[-/A]AAAAAAAAATGGTGA | 7525 |
rs553791530 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:791688 | TTTAACCTACTATAT[C/G]AAAAATGTTATCAAC | 7525 |
rs553805130 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:736570 | CATGTCAAAAGAAGT[A/G]TAAAGAGGCTACTAC | 7525 |
rs553813768 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:807483 | CAGTCTGGGCAACAG[A/C]GCAAGATCCTGTCTC | 7525 |
rs553818012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:754456 | TCACGCATGTAATCC[C/T]AGCACTTTGGGAGGC | 7525 |
rs553828923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:784223 | TACAAGTTTTCTATA[C/T]GCTCACCATATTAAA | 7525 |
rs553836729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:771204 | AAACCTCGTCTCTAC[C/T]AAAAATACAAAAATA | 7525 |
rs553860255 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:770235 | AGTGCTGGGATTACA[G/T]GTGCTGTGAGCCACT | 7525 |
rs553897257 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:764893 | GCACACCACCACACC[A/C]GGCTAATTTTTTGTG | 7525 |
rs553902660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:792300 | CAGAGTGAGACTTCA[C/T]CTCGAAAAACAAACA | 7525 |
rs553906852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:731296 | GGTAATAGAAGAATC[A/G]TCACCATGTGTATTA | 7525 |
rs553924071 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:810007 | ACAGAATTTCCTTGC[A/G]GGTTTTTTTTTTTTT | 7525 |
rs553930456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:754959 | AGACACTGAGTGTAC[A/G]CTGAGTTAATAAATG | 7525 |
rs553932088 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:803539 | TTCTATACCTCATAC[A/T]GTCCTATAGGGTTAG | 7525 |
rs554022108 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:741499 | CTGGTTCATCTAATA[G/T]ACTCTTTGAAAGGGC | 7525 |
rs554069410 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:805532 | CATGAGGCCCAACTA[A/C]CTTTTGTTTCAAATT | 7525 |
rs554105945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:799321 | CCTGCTAGAAACTAT[C/T]TTTTCCAGCTCTCCT | 7525 |
rs554195546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:735669 | CAGTGAGCCGAGATC[A/G]TGCCGCTACACTCCA | 7525 |
rs554258796 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:742172 | AGGCCTGTCAGCTTA[C/T]CTGCTGACTTACTAG | 7525 |
rs554432782 | snp | A/C/T | 0.00358938 | 0.0422398 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722960 | AGCCAGGCGTGGTGG[A/C/T]GGGCACCTGTAGTCC | 7525 |
rs554440149 | snp | C/T | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:721815 | TACTTTATAAAAATA[C/T]TAAGTTTAGGCTACC | 7525 |
rs554452351 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:742338 | GAAGGTAGTGGGGAG[A/G]CCAGGCACAGTGGCT | 7525 |
rs554462036 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:808145 | AAACCCAACGCAGAC[A/C]AGGATATATTGCCAT | 7525 |
rs554497964 | in-del | -/AGGAAGGCATTCCAGAT | | | intron-variant | YES1 | GRCh38.p7 | 18:736205 | ACAAACATTACAGAT[-/AGGAAGGCATTCCAGAT]GGAGGTAACTGTACA | 7525 |
rs554534971 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:733990 | TTTTATTTAAAAAGT[A/G]GCAGGTGGTTGGGCA | 7525 |
rs554545308 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:745424 | ATATTTGCTTTTAGG[C/T]TTATTTTCATAAGGT | 7525 |
rs554588849 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:728529 | ATTTTGGAGCATTTC[A/G]GTTTTTTTTCTCTTT | 7525 |
rs554619567 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:755309 | GCTGGAATGCAGTGG[C/T]GCAATCTTGGCTCAC | 7525 |
rs554623590 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722949 | TACAAAAAACTAGCC[A/G]GGCGTGGTGGTGGGC | 7525 |
rs554635015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:739104 | TGCTCAGATTACAAG[C/T]GTGAGCCACCGCACC | 7525 |
rs554650504 | snp | C/T | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724305 | CCATATCTGGGATTC[C/T]AGTTTACCATTAAAA | 7525 |
rs554654316 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:751973 | TTTAAAGTAGAGAGA[C/T]ATGACCATATTTTAT | 7525 |
rs554656721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:780606 | TTATAAATTAGCCAG[C/T]TTCAAGTATTCTGAA | 7525 |
rs554663304 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:752999 | ATAAAGTATAAATTC[A/T]AAAACTGTCATATTT | 7525 |
rs554678014 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:745108 | CATGGAAACATCCCC[G/T]CTCCTAGTATTAATC | 7525 |
rs554733658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:740670 | GGGACAAGTGCTAAG[C/T]GAATACCAAAATGAG | 7525 |
rs554763345 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:802357 | TGGATCACCTGAGGT[C/T]GGGAGTTCCAGACCA | 7525 |
rs554765983 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:763204 | GGAGATTTAATATAG[A/T]AGATTATTTGTTATG | 7525 |
rs554768027 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:747598 | TCAAGGCAGGGAATG[A/T]GGATAATCAGAAGGC | 7525 |
rs554768826 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:734804 | ATGGAAACTCCTTAA[A/C]GAACGAAAAGCAGAA | 7525 |
rs554783756 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:801753 | TAGACTTCACAAACC[C/G]AAACCTATAAAAGGG | 7525 |
rs554793420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:739911 | ACACAAAACTTCTTA[A/G]CTTTTCATTTTTTTT | 7525 |
rs554818761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775694 | CCCAGACACTTGGGA[A/G]GCTGAGGTTGGAGGA | 7525 |
rs554839312 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:808768 | TAGCAAGCCATTACA[C/T]AAAGCAAATAAAATA | 7525 |
rs554880108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:769512 | CTCAATCTTAAGAGG[A/G]AAGTATTTAGTCCAT | 7525 |
rs554882352 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:773782 | GCTGACTAATAAAAG[-/A]AAAAAATAAGAAAAA | 7525 |
rs554888509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:767519 | AAAAACCTATCCATT[C/T]CCCACTGAATTACCT | 7525 |
rs554913882 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:731244 | AGAGTGAAAGACAAG[A/T]TTACACAGGAGAAGA | 7525 |
rs554940836 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:771298 | TTTGAACCTAGGAGG[C/G/T]GGAGGTTGCAGTGAG | 7525 |
rs555017489 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:799033 | TAGTCAGATGCTCTG[C/T]TTTAAGAAACACATT | 7525 |
rs555037126 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:787874 | CCATAGATCGACATA[C/T]ATCAAATTAATTTAC | 7525 |
rs555082814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:752210 | CCTCCTAGGTTCAAG[C/T]GATTCTCATGCCTCA | 7525 |
rs555125020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:743821 | TGAGGCAGATGGATC[A/G]CATGAACCCAGGAGG | 7525 |
rs555136322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:757489 | GCCTGGGCGACAGAG[C/T]GAGACTCCGTCTCAA | 7525 |
rs555153172 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:756115 | TTAAATCAGCAGCAT[C/G]TGGGAGAAATTCTGT | 7525 |
rs555212897 | snp | C/G | 1.65792e-05 | 0.00287912 | intron-variant | YES1 | GRCh38.p7 | 18:743240 | AACAATGACAGAAAA[C/G]AAAAATTCAGGCTTC | 7525 |
rs555281826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:790459 | GTTTCTAATTCATTA[C/T]CTTTTCTTTTAATTT | 7525 |
rs555281830 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:782200 | ATGCTCATGTGCTTC[A/T]TTCTTCTCTCCTGTG | 7525 |
rs555285076 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:775025 | AGGTCAGAGACAGAG[C/T]GTCTGGGTGCAAAGT | 7525 |
rs555299211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:766511 | TATTCCCAACTCTAA[C/T]AGGAAGCAACCATTA | 7525 |
rs555303282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:761017 | AAAGGCCAATTAACA[C/T]ATGAAAATGCATCCA | 7525 |
rs555307370 | in-del | -/TA | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:746914 | GTATGTGTGTGCATG[-/TA]TATATATATACACAT | 7525 |
rs555344863 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:782753 | AGGTTGGAGTGCAGC[A/G]GCACAATCTCGGCTC | 7525 |
rs555346096 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:756089 | GTCTGAGCTTTAGGA[-/T]TTTTTCTTTTTTAAA | 7525 |
rs555456553 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:799187 | TATTTTCCATACAGA[C/T]GTCTAACTTGTGTAA | 7525 |
rs555464874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:811361 | AAAACAAAAACTAAA[A/G]TCCCTACACCAGACT | 7525 |
rs555485641 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | YES1 | GRCh38.p7 | 18:766075 | CCACTTGGTTAGTCA[A/C]CAGCCATTCTTCCTC | 7525 |
rs555507492 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:778959 | GTCGGTAATGGTACC[A/C]ATTTTTTACCATCTT | 7525 |
rs555509870 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:786600 | TTGCCAAAATTAATA[C/T]CATATCAGTTCAGGG | 7525 |
rs555625333 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:772832 | ACTTACTCATAATTT[G/T]TATTCATTTGTGGTC | 7525 |
rs555647452 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:794487 | ATATTATTAGGACAA[C/T]TGGAAAAATATATGA | 7525 |
rs555691717 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:793538 | GATGGGGTCTCACTA[A/C]ATTGCTCAGGCTGGT | 7525 |
rs555701326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:769480 | ACAAGTGAGGAGAGA[A/G]TATCTATGCCTTGGT | 7525 |
rs555707650 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:785584 | TATGGTTTGAATATG[A/C]ACCCAAAGTTCACGT | 7525 |
rs555733351 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:799367 | CCATATGACTTGCTT[A/G]TATCAATGTAATATA | 7525 |
rs555763838 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:811483 | GACAATTTTCTTTAA[C/T]ACATGTGGACAGGGA | 7525 |
rs555792782 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:800993 | TCTACTAAAAATATA[A/T]AAATTAGCTGGGTGT | 7525 |
rs555800190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:732128 | TACTGAAGAAAACAA[A/G]GCAAGTACATATTTA | 7525 |
rs555814671 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:772281 | TGATCCTCCCACTTC[A/G]GCCTCCCAAAGTGCT | 7525 |
rs555850421 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:768150 | CAGGCTCAGACAATA[C/T]GCACAACACACTAAG | 7525 |
rs555891091 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:768962 | CCTGCCTCAGCCTCC[C/G]GAAGTGCTGGGATAC | 7525 |
rs555901894 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:726567 | GGCGGATCACCTGAG[A/G]TCAGGAGTTTGAGAC | 7525 |
rs555913700 | in-del | -/ATC | | | intron-variant | YES1 | GRCh38.p7 | 18:765203 | AGATACGAAAAGATA[-/ATC]ATCAACTTCAAGACA | 7525 |
rs555955777 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:734330 | GAGGCCGAGGTGGGC[A/G]GATCATGAGGTCAGG | 7525 |
rs555968905 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:797741 | AACTTTCAGTGTCTG[C/T]ATTTATTAACGTTCA | 7525 |
rs556017800 | in-del | -/T | 0.00637571 | 0.0560999 | intron-variant | YES1 | GRCh38.p7 | 18:773180 | AATTTCCACATTAGA[-/T]TTTTTCTTTAATAGA | 7525 |
rs556037803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:767409 | GCCTGCCTCAGCCTC[C/T]CAAAGTGATGGGATT | 7525 |
rs556056485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:797083 | AAGGAACATTATGCA[C/T]AGACATGGAAAAGTC | 7525 |
rs556061150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:757222 | TACTTGAAAAAGTAT[C/T]GCTGGGCGCAGTGGC | 7525 |
rs556075568 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722229 | TCACAAGTTGTTGAT[A/G]AGAGGAAATAATGAC | 7525 |
rs556081461 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:763777 | GGAAATGAGAAGTGT[A/G]TAAGTATAATAATCA | 7525 |
rs556082240 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:753776 | AAGGTGTGAGCCACC[C/G]TGCCCGGCTGACATC | 7525 |
rs556094323 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:762188 | AGCTGGGCGTGGTGG[C/T]CCATGCCTGTAATCT | 7525 |
rs556103952 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:808740 | TGCAAAGCCACAATA[C/T]CAACCACTAAAATAG | 7525 |
rs556108248 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:759612 | AATAACGTACAGACT[A/T]TTTTTCCTTGTCATT | 7525 |
rs556139864 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:803354 | CATAGCACCTATCAT[A/C]GGACAGGCTTTCTTC | 7525 |
rs556142883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:757613 | ATCACTTGAGGTCAG[A/G]AGTTCAAGACCAACC | 7525 |
rs556217139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:758316 | AGAGTTGTATATGGC[C/T]AGTGGCTATCATACA | 7525 |
rs556240937 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:729771 | AGCTGGGATTACAGG[C/T]GCCCGCCACCATGGC | 7525 |
rs556255977 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776351 | GGCTCATGCCACCAC[A/G]CCTGGCCAATCTTTT | 7525 |
rs556274000 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775622 | AGCAACATAATGAGA[A/C]CTCATCTCTACAAAA | 7525 |
rs556296526 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:797857 | CAGAAATACCTTTCA[A/G]AACCTTGAGATATAA | 7525 |
rs556366579 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:771641 | GAAGCCTAGACCTCC[C/T]GGTCTCAAACTATCC | 7525 |
rs556379919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:811496 | AACACATGTGGACAG[A/G]GAACCGAACGCAACG | 7525 |
rs556398440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:810202 | TGCAAATTTCAACTT[C/T]GAATAAGTAAGTCTT | 7525 |
rs556399895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:747105 | TATTCTTTCATGGGC[A/G]TATTACTTTTATAAT | 7525 |
rs556427979 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:801714 | AGAGTGTGTATGTGT[A/T]TATACAGAGAGAGAG | 7525 |
rs556439639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:803928 | CTGCCTAGAAATCAG[A/G]CCAAAAGGCTTATGT | 7525 |
rs556460522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:810978 | TATTAGATTTACCAT[A/G]CACTTTTCCTTAAAT | 7525 |
rs556492636 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:774508 | CCCCAACTCGATAAA[C/T]GTTAACGCCATTCTT | 7525 |
rs556492739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:784080 | ATATTCATTTTAACA[C/T]ACATGTTGTCATACA | 7525 |
rs556500267 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:759455 | CTGGGCGACAAGAAC[A/G]AAACTCCGTCTCAAA | 7525 |
rs556545597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:730555 | TCCCTATGGTTCCTT[C/T]TCTGGGACCCTGTCC | 7525 |
rs556589943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:741348 | TCCTGGGCTCAAGCA[A/G]TCCTCATGCCTCAGC | 7525 |
rs556616249 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:782951 | CCTCCCGAAGTGCTG[C/T]GATTACAGGCGTGAG | 7525 |
rs556626089 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:742141 | TAAAGCAGATGAAAT[A/C]AAACACATAAAAATC | 7525 |
rs556627205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:794335 | ACTATACAAAACCAG[C/T]AGTCTAACTTTTAAA | 7525 |
rs556651275 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:807191 | GTACAAAAATTAGCC[A/G]GGCGTGGTGGTGCAC | 7525 |
rs556712478 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:774657 | CACCTCCCACTGCTA[C/G]CCTGGTCTAGGTCAC | 7525 |
rs556799407 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776989 | ATTTGTGGTTATGAA[A/T]AACAAAAAGGCCAAT | 7525 |
rs556845951 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:733381 | CTTTTTATATCATTC[G/T]GGAAAATTTTATTGT | 7525 |
rs556879255 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:804014 | AACTTTCAGAACACT[A/G/T]TAATTTTAGTTTCTT | 7525 |
rs556889110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:779985 | ACGCCTGTAATCCCA[A/G]CACTTTGGGAGGCTG | 7525 |
rs556895656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:744573 | TTTTTTTATATTTTA[A/G]TAGATAGGGTTTTGC | 7525 |
rs556931457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:751514 | CAGCAGCACAAATTG[C/T]AGAAGTAATAACTTC | 7525 |
rs556941017 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:771147 | AGGCAGGCAGATCAC[G/T]TGAGGTCTCAGGAGT | 7525 |
rs556943305 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812909 | GGCGTTACTCACACC[C/G/T]TCATCACCATCCTGA | 7525 |
rs556943929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:752060 | GACCTTCCATAAAAC[C/T]ACTGTATTCTACAAA | 7525 |
rs556945747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:738517 | AACACGGTGAAACCC[C/T]GTCCCTACTAAAAAT | 7525 |
rs556948727 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | YES1 | GRCh38.p7 | 18:738058 | TTTTTTTTTTTTTTT[A/T]AAAAACAAAAATGGA | 7525 |
rs556963775 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:780569 | TCTGCCTCCAGATCT[G/T]TAAGAAATAAATTCC | 7525 |
rs557028947 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:786424 | AAAATAGAATCTTTG[C/T]CTATTGTTGTGGTTA | 7525 |
rs557061164 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:750508 | AGAAGACAGCGGCAG[C/T]ACCCCAACTGTGACA | 7525 |
rs557073829 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:757359 | ATGCAAAAAATTAGC[C/T]GGGCGTGGTGGTGGG | 7525 |
rs557098963 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813510 | ACGGATAGGAAATAG[C/T]GCAATCATATGTGTC | 7525 |
rs557107325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:774460 | TCCAAGAAACCTAAT[C/T]TTCCTCCCCAAAGCA | 7525 |
rs557141468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:762382 | GAAACCTACCTGTTG[A/G]ATATTACACTGATTA | 7525 |
rs557164071 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:807676 | GTCCATCTTCTCAAA[C/T]GCCAGGGATAAAGAA | 7525 |
rs557192210 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:801614 | TATAATTAGTAGAAA[A/T]AAAGGCAATATTGTA | 7525 |
rs557196946 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:793874 | AGAAAAAAAAATGGT[A/G]ACACTAACAGATTAC | 7525 |
rs557199593 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:752903 | AGCCGAGATTATGCC[A/G]CTGCACTGTAGCCTG | 7525 |
rs557201481 | snp | C/T | 0.000181355 | 0.00952075 | missense | YES1 | GRCh38.p7 | 18:745776 | ATATAGTATCCACCA[C/T]TGTCAAGTTTCCTAA | 7525 |
rs557208610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:763136 | AACAGAAAATTTCTC[C/T]GTTCCAAGAGTGTGA | 7525 |
rs557239206 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:729825 | AGAGATGGGGTTTTA[C/T]CATCTTGGCCAGGCT | 7525 |
rs557243445 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:784029 | AAAACAGGCATAATA[C/T]GACGGAATTTCCCCA | 7525 |
rs557245667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:782136 | ATCTCTCCTTCACCA[C/T]CTCCATGTGTTTTAT | 7525 |
rs557291758 | in-del | -/TA | | | intron-variant | YES1 | GRCh38.p7 | 18:750923 | TTGCAAGTAATTCAG[-/TA]TATGTCTGGGTATTA | 7525 |
rs557341127 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:766789 | ATTTTTAATTGGGCT[G/T]TCTTCTTTCTGTTAT | 7525 |
rs557404004 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:749753 | TAGTCCCAGCTACTC[A/G]GGAGGCTTAGGCAGG | 7525 |
rs557409541 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722818 | TGAATGTAGGCTGGG[C/T]GCGGTGGCTCACGCC | 7525 |
rs557420232 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:795756 | ACTGGGGCCTGTTAG[C/G]GGGTGGGGGGAAGGG | 7525 |
rs557427987 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | YES1 | GRCh38.p7 | 18:747238 | ACTTTGGAAGGCTGA[A/G]GCGGGTGGATCACTT | 7525 |
rs557439457 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:762670 | CAACGTACACTACTC[C/T]GGTGACGGGTGCACC | 7525 |
rs557504482 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:777172 | TGGTGAAGTACAACA[C/T]AGAAGAACAAGAAGG | 7525 |
rs557508801 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:748851 | AGACAATTAACAATG[A/T]GCAACAAAGTTAAAA | 7525 |
rs557524087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:739298 | CACATTGGATTATCT[C/T]TGACGTTCCTGCCAG | 7525 |
rs557549411 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:806730 | AAGTGTTTTGTGGGA[A/G]CACAAAGAGGTCATA | 7525 |
rs557549595 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:790677 | GTTTTCAGAACTAGA[G/T]AAAATGGCTAACTAG | 7525 |
rs557552611 | in-del | -/TTA | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:759718 | ATTTCTTTTTTTCTT[-/TTA]TTATTATTATACTCT | 7525 |
rs557553749 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724223 | TTGGACCCTGAAATA[C/T]GCTGATAAATTCATC | 7525 |
rs557596573 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | YES1 | GRCh38.p7 | 18:759139 | CTCTCTTAAATTGGT[A/G]TATTCTAAAGATGTG | 7525 |
rs557597837 | snp | A/C | 0.000115339 | 0.00759318 | intron-variant | YES1 | GRCh38.p7 | 18:748054 | ATCACCGCAAGGTAG[A/C]CTATTGCCCAAGGTA | 7525 |
rs557598927 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:785155 | GTTATGCACAGACCT[-/T]TTTTTTTTTTTAACC | 7525 |
rs557682043 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:772221 | TTCAGTACAGACAGC[G/T]TTTCTCCATGTTGGT | 7525 |
rs557756458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:792488 | AGTCACACCTGTGAA[C/T]AGCACTATACTCCAG | 7525 |
rs557764832 | in-del | -/AAAA | 0.460702 | 0.134554 | intron-variant | YES1 | GRCh38.p7 | 18:726781 | CAAGACTCTTGTCTC[-/AAAA]AAAAAAAAAAAAAAA | 7525 |
rs557786508 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:810838 | TAAAACTTTCTTACT[A/G]TACAATATATGAACA | 7525 |
rs557816683 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:777847 | AAAAGAATTACCTAT[A/G]TCAGAACATACTTTA | 7525 |
rs557826107 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:765202 | TAGATACGAAAAGAT[A/T]ATCATCAACTTCAAG | 7525 |
rs557848306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:811632 | AAACCAAGTAAAGCC[A/G]GAAAGGCTCATCCAC | 7525 |
rs557860312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:764836 | CTCCTGGGTTCATGC[A/G]ATTCTCCTGCCTCAG | 7525 |
rs557878211 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:771610 | CTGGAGTGCAGTGGC[A/G]CGATCACGACTCACT | 7525 |
rs557878593 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:788780 | TTTTTTTAAAAATTA[A/G]CCAGACATGGTGGTG | 7525 |
rs557887490 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:760142 | GGTTCCAAGTCTTTG[C/T]TATTGTGAATAGTGC | 7525 |
rs557902047 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:798051 | TGGGGAAATCACAGG[A/G]GTCAGCACAACCAAA | 7525 |
rs557902148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:804504 | ATCCCAGCTACTGAG[A/G]AGGCTGAGGCAGGGA | 7525 |
rs557973186 | snp | C/T | 6.77209e-05 | 0.00581858 | synonymous-codon | YES1 | GRCh38.p7 | 18:743078 | TTTGATTGCTACTTT[C/T]GTGGTTCCATTCCAT | 7525 |
rs557993879 | in-del | -/TTAG | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:806578 | CAATTCAGAATTTAT[-/TTAG]TATTTATTGTGCTAA | 7525 |
rs558033017 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:792959 | TATTATATATCTATA[A/C]AGTTCAAGTCAACTT | 7525 |
rs558044150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:799912 | CAAAAACAAAAAACA[A/G]AAAAAAAAGAAGGTA | 7525 |
rs558054816 | in-del | -/CTGA | | | intron-variant | YES1 | GRCh38.p7 | 18:798438 | TATGAGTTTCTCCTT[-/CTGA]CTTACAGTGCATGCA | 7525 |
rs558081016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:774836 | CACTTAAAGTCAAAG[C/T]CAAAGTTCCTACTAT | 7525 |
rs558147418 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:765921 | AGTTGAAGAATAATA[A/T]GTGAGCCATGAAATG | 7525 |
rs558169850 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:811967 | CGATCCGGGGGAGGG[G/T]AGAAGTTTCTTCCCA | 7525 |
rs558170855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:808194 | GACAACAGTAGTGCT[A/G]CTGCAGCCAACGATT | 7525 |
rs558207753 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:781446 | AGGTCTTAGCTTAAA[C/G]GTTCAAGGAATCTTC | 7525 |
rs558231390 | in-del | -/TAAA | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:744044 | TGTTAGTATATTTAC[-/TAAA]TACTTAGTATAACTT | 7525 |
rs558234085 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722359 | GCCAACTTGCATGAA[A/G]TCCATCTTCACATTT | 7525 |
rs558268880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:774405 | ACTGTCTACGCAATA[C/T]CTTCACTTGGACGTC | 7525 |
rs558279954 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:768904 | GACAGGGTTTCCCCA[C/T]GTTGGCTGGGCTGGT | 7525 |
rs558291056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:731764 | CAAGGTCAGGAGATC[A/G]AGACCATCCTGGTTA | 7525 |
rs558356662 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:796519 | TCACGCTGGTAATCT[A/C]AGCACTTTGGGAGAC | 7525 |
rs558388349 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:757171 | TAGTAGTGGAGTGAT[C/T]TCAGGGTATGTTGCT | 7525 |
rs558433290 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | YES1 | GRCh38.p7 | 18:726146 | AACTTCACTCAAAGG[C/T]CGGGTGCGGTGGCTC | 7525 |
rs558434523 | snp | C/T | 1.65269e-05 | 0.00287457 | missense | YES1 | GRCh38.p7 | 18:743404 | ACTTGTGGCATAAAC[C/T]ATCAGCATGTTCTAG | 7525 |
rs558441423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:802492 | GAGGTTGCAGTGAGC[A/G]GAGACCACACTATTG | 7525 |
rs558449222 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721500 | CCAAGATCGCGCCAC[C/T]GCACTCCAGCCTGGG | 7525 |
rs558475935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:726468 | TCTTCAGAATTTTCT[A/G]ATAATTAGAACTATT | 7525 |
rs558541023 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:763370 | AGCAGTTAGACAAGT[G/T]ATAAAACTATTCCAA | 7525 |
rs558551758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:768771 | GCAGTGGTGTGATCT[C/T]GGCTCACTGCAACCT | 7525 |
rs558600964 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722958 | CTAGCCAGGCGTGGT[A/G]GTGGGCACCTGTAGT | 7525 |
rs558609324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:763728 | AAAAAAAAAAAAAGA[C/T]GAGCTGGAACAGTGT | 7525 |
rs558624929 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:745235 | AGACAAAAATGTCTA[C/T]AATTGCTATAGGTTA | 7525 |
rs558634327 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:734309 | CCTGTATTCCCAGCA[A/C]TTTGGGAGGCCGAGG | 7525 |
rs558643982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:782855 | GTGCACCACCATGCC[C/T]GGCTAATTTTTGTAT | 7525 |
rs558658177 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:747057 | GTGCTTAAATGAAGA[C/T]ATTAACAGTCATATA | 7525 |
rs558658983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:739209 | TCTAATACTCGTTCT[A/G]TTACTAACAAGTTTT | 7525 |
rs558659299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:806246 | TTCTTCACTAAAATA[A/G]TACAACGTATTTATT | 7525 |
rs558697606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:734048 | ATTTGAGAGGCCGAG[A/G]TGGGCAGATCACCTA | 7525 |
rs558716934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:740798 | GAATTTTACCATGTT[C/T]TCCCAATTAAATAAT | 7525 |
rs558762081 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:737838 | AATTTTCCCACCTCA[A/G]CCTAGTGAGTAGCTG | 7525 |
rs558763939 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:748398 | AAGGTGTAATTTGCA[C/T]GCCATAAAATTCCCC | 7525 |
rs558775117 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:730522 | ACTGGAATTTTAAAG[C/G]AGAATTTTAGAGTTC | 7525 |
rs558777544 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:757540 | AAAAGTATCTGGGGG[G/T]CCAGGCGCAGTGGCT | 7525 |
rs558782748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:790604 | GTATGAGAAGGGTAC[C/T]AGAGCCACAGATGAT | 7525 |
rs558785776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:758187 | TATTTCAACATGTAA[C/T]CGATATAAACATTTT | 7525 |
rs558789688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:753236 | GCTTTGAAATATATA[C/T]ACATTGTGGAATGGC | 7525 |
rs558799317 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:734834 | ACTACCATTCAATCC[A/C]GCAAACCCACTACTG | 7525 |
rs558825456 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:774974 | CAAGCATACTCCCAG[C/G]TTATTGTATGTATGG | 7525 |
rs558833379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:735219 | TGTTTATAGCAGCAC[A/G]ATTCGCAATTGCAGA | 7525 |
rs558834846 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:729910 | GATTACAGGCGTGAG[A/C/T]CACAGCGCCCAGCCA | 7525 |
rs558902912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:764546 | AGTTTTAACCAAGTG[A/G]AGAGTAACACCATAA | 7525 |
rs558923816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:810086 | ATTGTTTTGGCATTA[A/G]TCTTCTTTCTTACTA | 7525 |
rs558936250 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:798316 | TATCTCTAAGAATCA[C/T]CAATATTGTTTTTCC | 7525 |
rs558959061 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:736467 | GACATTGTCAGATGT[C/G]CCCTGGTGAGTGGCG | 7525 |
rs558976614 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:746543 | GCTATGGAAGAGCTC[A/C]CAGAAAATGAGAAGA | 7525 |
rs558988048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:742508 | AAAGTTCCTAGAAGT[C/T]CTGAATATAGGAATT | 7525 |
rs558988876 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:788777 | ATATTTTTTTAAAAA[C/T]TAGCCAGACATGGTG | 7525 |
rs559009340 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:790094 | AAACAAAAGATTCCC[A/G]GCTGAGTGCAGTGGC | 7525 |
rs559048998 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:771343 | CTACACTACAGCCTG[C/G]GGAATAAGAGCAAAA | 7525 |
rs559057970 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:753739 | GATCTACCTGAGTCG[C/G]CCTCCCAAAGTGCTA | 7525 |
rs559090798 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | YES1 | GRCh38.p7 | 18:782752 | CAGGTTGGAGTGCAG[C/T]GGCACAATCTCGGCT | 7525 |
rs559140230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:756222 | TACAATCCTGAGAAG[C/T]TGTCAAATTCTTGAG | 7525 |
rs559153376 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:741775 | CACTCCACCCTGGGG[A/G]ATAGAGTGAGGCCCC | 7525 |
rs559154568 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:758543 | CCCCTTCTAAAATTG[C/T]CTCTGTTCCAAGTAT | 7525 |
rs559168052 | in-del | -/TGA | 0.00597247 | 0.0543191 | intron-variant | YES1 | GRCh38.p7 | 18:729939 | CAGATTTTGAACTCT[-/TGA]TAATCAGTCATCTCT | 7525 |
rs559176707 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:741191 | GCATGAACCACTGTG[A/C/G]CTGGCCTGCTTCCAA | 7525 |
rs559195677 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | YES1 | GRCh38.p7 | 18:731823 | ATACAAAAAATTAGC[C/T]GGGCGTGGTGGCGGG | 7525 |
rs559254312 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:753243 | AATATATATACATTG[C/T]GGAATGGCTAAGTAG | 7525 |
rs559260714 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812385 | GGGGCTGCGGGTACC[A/T]GCGCGCGCCGCCGTC | 7525 |
rs559271876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775784 | CCTGGGTGACAGAGT[A/G]AGAACTTGCCTCAAA | 7525 |
rs559322185 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:810048 | AAGTTTGGGTGACCC[C/T]AGCGCTTAGCATCAC | 7525 |
rs559332025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:726610 | CATGGCGAAACCCCC[C/T]CTCTACTAAAAATAT | 7525 |
rs559332955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:769658 | AAAAGCTTTTCTACA[C/T]GTACTTAGATTATCA | 7525 |
rs559380772 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:741242 | CCTGTCCTTTTCTCC[-/T]TTTTTTTTTTTTTCT | 7525 |
rs559484402 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:773224 | ATCTGGAAGATTAAT[A/G]TTTAATGCTGATCCA | 7525 |
rs559488955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:750718 | CAGGGGATAAGGACT[A/G]GGCCAGGCAGGGGAG | 7525 |
rs559515965 | snp | A/C | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775898 | TCTCTATTATCAGGA[A/C]CAGCTGTACTTTGTT | 7525 |
rs559565527 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:805857 | CCAATTTCTACTTAA[A/T]GCTAAGAAACTGAAA | 7525 |
rs559606976 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:779358 | GCGGTAAGTTATGAT[C/G]GCACCACTGCACTCC | 7525 |
rs559619769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:780096 | AAAATTAGCCAGGCG[C/T]TGTGGCACGCACCTG | 7525 |
rs559637150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:765558 | CGTGTACCACCACAC[C/T]CAGCTAATTTTTTGT | 7525 |
rs559700796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:744131 | ATTGTGCTAAATTAG[C/T]ACTTCACAAGTATCT | 7525 |
rs559735874 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:785982 | TAACCCTCTCTCAGC[C/T]TCTTGCCTTCCACCA | 7525 |
rs559761532 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:744735 | GATGAGGTCTTGCTA[A/T]GTTGCCCAGGCTGTT | 7525 |
rs559784130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:786893 | AGGTTACATGATTTA[C/T]TTAAAAAAGCTCATA | 7525 |
rs559809352 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:793996 | GAGTAAGAGAGCTAC[A/C]CATTCAGCACACGTA | 7525 |
rs559843421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:757722 | AGCTACTAGGGAGGC[C/T]GAGGCATGAGAATCA | 7525 |
rs559880885 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:753436 | CATATTTTTAATTTG[A/C]ATATGTATATACTCT | 7525 |
rs559894806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:746683 | TCATATACAAGGTAC[A/G]GTGTTAAGTGTTATA | 7525 |
rs560017791 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:783088 | CCTAAGAATATTTTT[A/T]AAAATTATATAGCCA | 7525 |
rs560024215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:733065 | CAATATCTCTACTGT[A/G]GTCATCAGTGTCAAT | 7525 |
rs560031666 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:729275 | CATTTGAGGGCCAGG[A/C]GGGGTGGCTCACGCC | 7525 |
rs560059420 | in-del | -/T | 0.454784 | 0.1434 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776198 | TTGGTATACTCGATC[-/T]TTTTTTTTTTTTTGA | 7525 |
rs560062292 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:804110 | GTTCTAAATATTAAC[C/T]GTATGTGTATAAAGA | 7525 |
rs560095557 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:731932 | AGATCGTGCCACTGC[A/C]CTCCAGCCTGGGCGA | 7525 |
rs560095568 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:753890 | CCAAGTCTTTCCTAT[C/G]TAAGTAAATGGCCCT | 7525 |
rs560193452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776432 | ATTTTATGTTCATAA[C/T]TACTAATGAAGTGGC | 7525 |
rs560246527 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:733238 | TAGAGGTTGAAGCTC[C/T]AGTAAGCCAAAGATA | 7525 |
rs560253740 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722995 | TACTCGGGAGGCTGA[C/G]GCAGGAGAATGGTGT | 7525 |
rs560260809 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:740959 | CTGGAGTGCAGCGGT[A/G]TCATCTTGGCTCACT | 7525 |
rs560358839 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:747207 | AGGCACAATGGCTCA[A/C]GCCTGTGATCCTAGC | 7525 |
rs560373857 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:804703 | GGATCACCTGAGATA[G/T]GGAGTTGGAGACCAG | 7525 |
rs560385698 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:791035 | CGGGTGGATCATCTG[A/G]GGTCAAGAGTTCGAT | 7525 |
rs560393090 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723269 | TTATAGTTATACTTT[A/G]TAACTCTTCAAAGTC | 7525 |
rs560448718 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:764705 | TAGATTAAACAAAAA[G/T]AGTTTCATAATTTAT | 7525 |
rs560449945 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:740234 | TACTGCTGTGACCAA[C/G]CTCTCTCTCTGAAAA | 7525 |
rs560483269 | in-del | -/A | 0.0023933 | 0.0345097 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724107 | ATTCTGACTTTGGGG[-/A]AAAAAAGAAAGGAAA | 7525 |
rs560493885 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:759194 | AACCGGGGCTAGGCG[A/C]GGTGGCTCACGCCTG | 7525 |
rs560509705 | in-del | -/AATA | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:811194 | GGAACGTATATACAT[-/AATA]AATGGACATAAAATT | 7525 |
rs560528207 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:730728 | CAGTTCTTTTACATA[A/T]TTTATTTAACTTTTG | 7525 |
rs560533399 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812946 | TCCAAAAAACGTTCA[C/T]GTCTTGCCTCCTTCC | 7525 |
rs560555151 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:766185 | CAGCCCTACGTAGTA[A/G]ATATTGATTTATTTA | 7525 |
rs560584816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:798236 | TAAACTATGTGTTCT[A/G]TGTCACCTATTATTT | 7525 |
rs560599445 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:807051 | CAGGCAGGTGGACTG[A/C]TGGAGCCTAAGAATT | 7525 |
rs560605518 | in-del | -/GGAGGT | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:801072 | AATCGCTTGAACCAA[-/GGAGGT]GGAGGTTGCAGTGAG | 7525 |
rs560612815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:764254 | TGAGACTGAGTCTCA[C/T]TCTTGTTGCCTAGGC | 7525 |
rs560617076 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:764106 | GCCTGGGCGACAGAG[C/T]GAGACTCCCTCTCAA | 7525 |
rs560618834 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:795821 | CGGGGCTTAAGACTA[A/G]ATGACGGGTTGATAG | 7525 |
rs560624133 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812465 | TTCCGGCGCCTACGC[C/T]CCCGTCAGGTCCCCT | 7525 |
rs560629923 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:792319 | GAAAAACAAACAAAC[A/G]AATAAATAAAGAAGT | 7525 |
rs560649561 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:754621 | GAGGCTAAGGCAAGA[A/G]AATGGCTTGAACCTG | 7525 |
rs560677962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:770811 | GTGTTTGTGGAGGTG[C/T]GGGGGTTGACAGATG | 7525 |
rs560739398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:748469 | AGAGTTGTACAACCA[C/T]TATCACAATCAATTT | 7525 |
rs560744213 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:800310 | TGTGTCATTGTTCTA[C/T]GTGCTTGGAACAACT | 7525 |
rs560749131 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:727625 | TAGTTATCATTGAGA[C/G]TACAATATGCTTCCT | 7525 |
rs560773557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:792616 | ATATATATACATACA[C/T]ATATATACGCACACA | 7525 |
rs560792970 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:759547 | TGAGTTCTGCATCCA[C/T]GGATTCAGCCAAGAT | 7525 |
rs560801333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:780016 | AGGAGGGTAGATTAC[C/T]TGAGGTCAGGAGTTC | 7525 |
rs560821852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:766929 | TCATAGGTTGCCTTT[A/G]CATTTCCATAACAGT | 7525 |
rs560842429 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:755395 | CTGGGACTACAGGTG[C/T]GCAACACCACACCTG | 7525 |
rs560862171 | snp | A/G | 0.0020012 | 0.0315689 | intron-variant | YES1 | GRCh38.p7 | 18:773180 | AAATTTCCACATTAG[A/G]TTTTTCTTTAATAGA | 7525 |
rs560902838 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:734983 | GCCAACATGGTGAAA[C/T]CGTGTCTCTACTAAA | 7525 |
rs560918128 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:738123 | AGAAGCATGAACTGG[A/C]GTGGCATATGCCTGT | 7525 |
rs560926817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:726893 | TACCAAGGTTTATTA[C/T]TATCCCCAAATAAGA | 7525 |
rs560949965 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:751593 | CGTTAAACACAGTGG[A/G]CAGCCCATGCCCTAC | 7525 |
rs560960017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:739353 | GTAATCCCAATACTT[C/T]GGGAGGCTGAGGTGG | 7525 |
rs561007754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:766373 | ACTTGCTCCACATCC[C/T]TAAGACTTGTTATTA | 7525 |
rs561016644 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:772519 | CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAG | 7525 |
rs561068616 | snp | A/T | | | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721434 | TCCCAGCTACTCGGG[A/T]GGCCGAGGCAGGAGA | 7525 |
rs561096578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:763483 | AAAGATTGCTTGAGC[C/T]TAGAAATTTGAGAGC | 7525 |
rs561159580 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | YES1 | GRCh38.p7 | 18:757420 | AGGCAGGAGAATGGC[A/G]TGAACCCGGGAGGCG | 7525 |
rs561161544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:763819 | TAAATATGGAAAGAG[A/G]AGACATTAAGAAAAA | 7525 |
rs561197120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:800876 | ACAAAGGCTGGGTGT[A/G]GTGGCTCACGACTGT | 7525 |
rs561213106 | snp | C/G | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722594 | TAGACACTCAAACCA[C/G]TAATGCTGCTATTCA | 7525 |
rs561224368 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:728750 | AGGATGGTCTCAAAC[C/T]CCTGACCTCGTGATC | 7525 |
rs561233844 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:775009 | ACAGTTAAGAGCATA[C/G]AGGTCAGAGACAGAG | 7525 |
rs561262141 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:757272 | ACTTTGGGAGGCCAA[A/G]GCGGGCGGATCACGA | 7525 |
rs561302533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:773859 | TTTTTTGAGACGGAA[C/T]CTTGCTCTGTCGCCC | 7525 |
rs561348611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:733627 | TCTCTACCAAAAATA[C/T]AAAAAATTAGCTGGG | 7525 |
rs561349343 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:791793 | GGCGTGGTGGCTCAC[A/G]TCTGTAATCCCAGCA | 7525 |
rs561355568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:742435 | ACCAGCCTGGGCAAC[A/G]TAGTTGAGACCCCAG | 7525 |
rs561374159 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:734172 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 7525 |
rs561405258 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:774503 | ATCTTCCCCAACTCG[A/G]TAAATGTTAACGCCA | 7525 |
rs561451571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:808361 | AGCAGCTGCAGCTGA[A/G]CAATACTCAGCCTAA | 7525 |
rs561463700 | in-del | -/T | 0.185788 | 0.241613 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:814131 | TCTCTTCGCCCTCCC[-/T]TTTTTTTTTTTATTA | 7525 |
rs561468322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:768432 | TTTTATTTATTTGGG[C/T]ATTTACAGACTTTTC | 7525 |
rs561481957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:747684 | TTAAGTGAAAACATA[A/G]AAGAGAGAGACTAGG | 7525 |
rs561493837 | snp | C/T | 0.00478085 | 0.0486577 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722908 | CTATCCTGGCTAACA[C/T]GGTGAAACTGCGTCT | 7525 |
rs561554882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:729369 | GCAGTGAACCAAGAT[C/T]GTGCCACTGTACTCC | 7525 |
rs561577902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:802184 | TGCCGAGGAGTTCGA[A/G]GCTGTAATGAGCTAT | 7525 |
rs561627839 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | YES1 | GRCh38.p7 | 18:770984 | GCACTCTGCTCTGGG[A/C]AATGAAGAGATATCC | 7525 |
rs561640476 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:757366 | AAATTAGCCGGGCGT[A/G]GTGGTGGGCGCCTGT | 7525 |
rs561696917 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:809593 | GTGTGAGCCACCGTG[-/C]CCCAGCCTGACGTGT | 7525 |
rs561699077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:784474 | ATTAATTATTGCTGC[C/T]ACAACAAATTACCAC | 7525 |
rs561699864 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:731783 | CCATCCTGGTTAACA[C/T]GGTGAAACCCCGTCT | 7525 |
rs561760298 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:791916 | AAAAATCAGCTGGGG[A/G]TGTTGGCGTGCACCT | 7525 |
rs561760645 | snp | A/T | | | utr-variant-5-prime | YES1 | GRCh38.p7 | 18:812136 | CCGGCCGCGCTCTCA[A/T]GAGTCGCTGCTACCG | 7525 |
rs561762691 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:731791 | GTTAACACGGTGAAA[A/C]CCCGTCTCTACTAAA | 7525 |
rs561779956 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:793318 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC | 7525 |
rs561784802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:792588 | GTGTGTGTGTGTGTA[C/T]ATACATATATACATA | 7525 |
rs561910144 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:811675 | CCCGCTCCTCTCCCC[A/G]CACAGCTGCTACCGG | 7525 |
rs561971400 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:735743 | AACAAAAAAACCTAC[A/G]TATTGGGTACAGTGC | 7525 |
rs561972515 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:800045 | ACAAGCTATTAAACT[A/G]CATCAAACCTTAGTT | 7525 |
rs561988203 | in-del | -/C | 0.00557542 | 0.0525036 | intron-variant | YES1 | GRCh38.p7 | 18:727717 | CCTCTTATTCCCTGA[-/C]CCCCTCTACCCTTTG | 7525 |
rs561999661 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:798947 | TCACTAGCTTTTTTT[C/T]CTACTGATCCTAATT | 7525 |
rs562005531 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:787288 | TATTTTTAGTAGAGA[C/T]AGGTTTCACCATATT | 7525 |
rs562011411 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:777260 | CCTTCTATTTAGCAC[G/T]AATTGTTTTATATAT | 7525 |
rs562036855 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:785415 | ATAATACTGAGTGTT[A/C]GGGGGGAGAAAGAGA | 7525 |
rs562039292 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:793870 | ATCAAGAAAAAAAAA[C/T]GGTGACACTAACAGA | 7525 |
rs562049465 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:785955 | AAGTGAGTTTCTCTC[C/T]CTCCCTCACTCTAAC | 7525 |
rs562132250 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:726085 | CAATCCAAATAAGCC[A/G]GAACCTATGAAAATA | 7525 |
rs562147122 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:804523 | CTGAGGCAGGGAGAA[C/T]TGCTTGAACCCGGGA | 7525 |
rs562168924 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721265 | ACCACAGGCCGGGCG[C/T]GGTGGCTCACGCCTG | 7525 |
rs562231731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:768358 | TTAATCTATAGATCA[A/G]TCTGGGGAGAAATGA | 7525 |
rs562233237 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:799460 | CACGCCTGTAATCCC[A/T]GCACTCTGGGAGGCC | 7525 |
rs562280202 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:749796 | ACCCAGGGGGCAGAG[A/C]TTGCAGTGAGCCGAG | 7525 |
rs562302266 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:757405 | CTACTCGGGAGGCTG[A/C]GGCAGGAGAATGGCG | 7525 |
rs562324919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:802003 | CAGTTGTTAGTGTAA[C/T]AACACATCTTTTTCA | 7525 |
rs562398645 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:796568 | AGGTCAGGAGCTCAA[A/G]ACCAGCCTGCCCAAC | 7525 |
rs562399060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:789302 | AAAAGAACAACTTTG[C/T]GAGGCATGGTGACTC | 7525 |
rs562408403 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:762185 | ATTAGCTGGGCGTGG[A/T]GGCCCATGCCTGTAA | 7525 |
rs562487921 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:752682 | TCACAGTGGTTCACG[A/T]CTGTAATCTCAGCAC | 7525 |
rs562488282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:763460 | AGCATTTTGGGAAGC[C/T]GAGGTGGAAAGATTG | 7525 |
rs562488732 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:760813 | AGAGGGGCAGGGGTG[A/G]GGACAGAAGTTTAAG | 7525 |
rs562535993 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:729468 | TGATTCTTTTTTTTT[A/T]AATAGATTCCAATTC | 7525 |
rs562536640 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722855 | CCCAGCACTTTGGGA[A/G]GCCGAGGCGGGCAGA | 7525 |
rs562540758 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:728831 | GCCCAGCTGCATTTC[A/G]GATTTTTGAATTAGG | 7525 |
rs562557495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:740197 | AACTAAATATAGGTA[A/G]CTAAATGAGTCGCTG | 7525 |
rs562561797 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:801432 | TAGAAGTATAGCCTT[G/T]AATGGCTGATGAGTC | 7525 |
rs562570692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:730133 | TCAGTTTTGCCCTTT[C/T]TCCTAGGGTATGGAC | 7525 |
rs562572795 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723032 | GGGAGGCAGAGCTTG[C/G]AGTGAGCCGAGATCG | 7525 |
rs562573614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:782335 | ATTCCTAATTCCTAA[A/G]GGACCCTGGCCCAGC | 7525 |
rs562653145 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | YES1 | GRCh38.p7 | 18:757325 | TGGCTAACACGGTGA[A/C]ACCCCGCCTCTACTA | 7525 |
rs562681950 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:739551 | AAGGCTCTTCAAGCA[C/G]GGAGCTATCAGTGCA | 7525 |
rs562765698 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:747275 | AGGAGTTTGAGACCA[C/G]CCTGGCCAATAGGCG | 7525 |
rs562805084 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:753282 | AACGTATGCATTGCA[C/T]CACATATCATTTTTG | 7525 |
rs562808703 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723244 | ATTTAGTGTGTAAGA[A/C]AAATTAGTTTTATAG | 7525 |
rs562821891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:781884 | CTTGGTTAAGACTTA[C/T]GGCTTCAAGGACAGA | 7525 |
rs562838663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775325 | ACAAAGAAAAATAAA[C/T]GTACAAGTGAATGAA | 7525 |
rs562840071 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:745887 | AATACTTTCACTATA[A/T]CTTTCTCAAAATACT | 7525 |
rs562840098 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:769785 | AAACCCAATTGGTCA[C/T]GGTATATTACCCTTT | 7525 |
rs562843504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:763902 | CGAGGCGGGCAGATC[A/G]TGAGGTCAGGAGATC | 7525 |
rs562845983 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724288 | AAAGTGGTTTTGTGC[A/C]ACCATATCTGGGATT | 7525 |
rs562848420 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:791912 | ATACAAAAATCAGCT[C/G]GGGGTGTTGGCGTGC | 7525 |
rs562893688 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:734870 | CTTCCCAAAGGAAAT[A/G]AAATCAGCCAGGTGT | 7525 |
rs562901062 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:754110 | CCCACACAGATGTCA[C/G]AGTCAGTTTTTCTCA | 7525 |
rs562951469 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:744030 | ATATATAGTAGATAT[C/G]TTAGTATATTTACTA | 7525 |
rs562960359 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:796254 | AGGTTACAGTCCTAG[C/T]GTGTAATTTGAGTAA | 7525 |
rs562976333 | snp | A/C | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:732448 | TTTAAAAAAAAAAAA[A/C]AAAAAAAAACAAAAC | 7525 |
rs563005617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775865 | ACCTCTTTCACTTAA[C/T]GATGCTTCTGAGACT | 7525 |
rs563056216 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:799305 | ACTGGGAGGTGGCTG[A/T]CCTGCTAGAAACTAT | 7525 |
rs563105196 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:791211 | GCCAAGATTGTGCCA[C/T]TGCACTCCAGCCTGG | 7525 |
rs563164448 | snp | A/C | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:750039 | ATGGGATTTGTTACT[A/C]AAGATTAAATTCATG | 7525 |
rs563193736 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:797358 | GAAAATATAGAAAGA[A/G]CTTTAAACCTGCTAA | 7525 |
rs563214713 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:726718 | CCTGGGAGGCGGAGG[C/T]TGCAGTGAGCAGAGA | 7525 |
rs563218316 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:804182 | AAAATTAAATGTAAA[A/T]TTTGATGATAGTGGC | 7525 |
rs563223872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:764629 | TTTTAGGTTCATGCT[A/G]TGAAGTCTGGTGGGG | 7525 |
rs563248747 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:779206 | CAGCAGTTCAGGACC[A/T]GCCTGGGCAACAAAA | 7525 |
rs563249156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:765687 | ACAGGCGTGAGCCAC[C/T]GCACCCGGCCAATTT | 7525 |
rs563249161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:772495 | TAGAGTGCAATGGTG[C/T]GATCTCGGCTCACTG | 7525 |
rs563293493 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:737218 | ATTAATTTGGGAGGC[C/T]GAGGCAGGTGGATCA | 7525 |
rs563297703 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:761891 | ATGGGTTGTCTTAGA[A/C]ACGTTAACATCATGG | 7525 |
rs563300196 | snp | G/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812426 | AACTCGGGCCACGCC[G/T]GCCCGGCTCCGGGGC | 7525 |
rs563348483 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:745167 | GCCAAATTGGTAATG[A/G]AAAATTTTGAGACAG | 7525 |
rs563353349 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:736625 | TACCTAGTCAAGTTC[G/T]TTCTTGGAGGAAATA | 7525 |
rs563381178 | snp | C/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722346 | TACCAGAACCACTGC[C/G]AACTTGCATGAAGTC | 7525 |
rs563384478 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:771864 | AGTATTTCCTTATGT[A/G]TCTGCTTGGTAAGTC | 7525 |
rs563390055 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | YES1 | GRCh38.p7 | 18:757274 | TTTGGGAGGCCAAGG[C/T]GGGCGGATCACGAGG | 7525 |
rs563444033 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:760183 | CAATTTAAAGCATAC[-/A]GGGGGACTGGGCACA | 7525 |
rs563453845 | snp | A/C/G | 0.00046114 | 0.0151779 | missense | YES1 | GRCh38.p7 | 18:756721 | GGTGACACTGTAGTG[A/C/G]GTTCTGCTCCATAAT | 7525 |
rs563454492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:800141 | GCACAAGTCTGCCAC[C/T]TCAAAGAGTCTTGAG | 7525 |
rs563515939 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:800836 | GGGAGGATCATGCTC[A/G]GCCCCATCTCTGGAA | 7525 |
rs563560889 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:766233 | TATCTCTATTGCCAG[C/T]TGGCTAGTTGAGCCA | 7525 |
rs563566139 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:787871 | AATCCATAGATCGAC[A/G]TATATCAAATTAATT | 7525 |
rs563617481 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:740508 | ACCATAAACTGGATC[A/G]GGGAAGTGTAGTTGG | 7525 |
rs563622131 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:752764 | CCTGGTCAACAGGGC[A/G]AAACCCTGTCTGTAC | 7525 |
rs563634404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:773305 | GACAGCTTTACTTTG[C/T]TCCCTCCTCATACCT | 7525 |
rs563645300 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:761197 | GAAAGGTCTACTGTT[C/G]CCCACCCCACTTTCT | 7525 |
rs563646233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:773720 | GCAAACTTTGTTCCA[A/G]CTTTCCTATGTTTCT | 7525 |
rs563723100 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:733510 | GGCTTTCGGCCGGGC[A/G]CGGTGGCTCAAGCCT | 7525 |
rs563727309 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:794590 | TTAAAATAACAAATT[G/T]ATTATGTCATAGTTC | 7525 |
rs563734852 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:780194 | CATGCCACTGCCCTC[G/T]GCACTCCAGCTTGGG | 7525 |
rs563744391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:747582 | TAAGTTAAAAAATAA[A/G]TCAAGGCAGGGAATG | 7525 |
rs563823851 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:781001 | TGGCCAGGGGCGGTG[C/G]CTCACGCCTTCAATC | 7525 |
rs563868712 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:753957 | AGTGCTATCAGTTTT[A/C]CCTCTAAAATACTAT | 7525 |
rs563876093 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:814272 | TATTTTTTAAAAAAT[G/T]TTTTAATGAGGAAGA | 7525 |
rs563902579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:728300 | CCACTGCACTCCAGC[C/T]TGGGTGACAGAGACC | 7525 |
rs563911902 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:770930 | GTGGGAGAACAGCTT[A/G]AGGGCAGTGACTGTT | 7525 |
rs563917802 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:747254 | GCGGGTGGATCACTT[G/T]AGGTCAGGAGTTTGA | 7525 |
rs563945977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:741008 | GCTCAAGCCATTCTC[A/G]TGCCTCAGCCTCCCG | 7525 |
rs563946534 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:811593 | AAACAAAGGAAAACT[C/T]TAAACATGTTGCGGT | 7525 |
rs564039147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776124 | TTTCCAGAGTAGCTA[C/T]AGCAGTTTATACTCT | 7525 |
rs564068954 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:757376 | GGCGTGGTGGTGGGC[A/G]CCTGTAGTCCCAGCT | 7525 |
rs564121652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:797284 | AATTTTAAGATATCT[C/T]TATTCATATATATAA | 7525 |
rs564150037 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:733052 | GCTAATGTTCTGTCA[A/G]TATCTCTACTGTAGT | 7525 |
rs564182210 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:798821 | TTTCCAATGTTTCCT[A/C]AAGTCTAGTGCACAC | 7525 |
rs564270008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:735512 | AAGGTTGGGGGGTGG[A/G]TAAAAGACTACATGT | 7525 |
rs564277756 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:763922 | GTCAGGAGATCGAGA[A/C]CATCCTGGCTAACAG | 7525 |
rs564304866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:730813 | AACTGAAAGTTCCTC[A/G]TGGTTATACATTTAA | 7525 |
rs564363338 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:741552 | CTCACACCTGTAATC[C/T]CAGCACTTTGGGAGG | 7525 |
rs564378270 | in-del | -/CCCC | 0.0298908 | 0.118541 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812328 | TCTCCACCTCCTCCG[-/CCCC]CCCCCCCCGGCCCCG | 7525 |
rs564392348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:792683 | GCAGCAGCAGCAGCC[A/G]TGTGCAGTGGCTCAA | 7525 |
rs564403980 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | YES1 | GRCh38.p7 | 18:783786 | TGCCCAGCTAATTTT[C/T]GTATTTTTAGTAGAA | 7525 |
rs564455958 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:793200 | GCATGCCACCATGCC[C/T]GGATGATTTTTTGTA | 7525 |
rs564485944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:804790 | GTGGTGGCACACGCC[C/T]GTAATCCCAGCTACT | 7525 |
rs564488803 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:792168 | GTTTAGCCAAGTGTG[A/G]TGGTGCATGCCTGTA | 7525 |
rs564519404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:742682 | TTTCCATTTGTTTTA[A/G]TCAAACTTAATTTCA | 7525 |
rs564541493 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:731369 | GGACAATGGTGAGTC[A/C]TTAAATGAGAATAAC | 7525 |
rs564579703 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:801333 | GTGACACCCTGTCTC[A/G]AAAAAATGATTTACA | 7525 |
rs564616492 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:773645 | CTAGACTTTCATAAT[C/T]CTGTCCATTGTATAA | 7525 |
rs564632092 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:789892 | TGGTGAAACCCCGTC[C/T]CTATTAAATACAAAA | 7525 |
rs564681284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:762658 | ATATACTGGGTACAA[C/T]GTACACTACTCCGGT | 7525 |
rs564736715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:785196 | TTGTTAGTTTTATTG[C/T]ATTTTATGTGTGGCC | 7525 |
rs564788389 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:801860 | AAAAAAGAAACTTGA[G/T]TGGGAAAACATGCTC | 7525 |
rs564803542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:755951 | CTCCACGAAAGGTTG[C/T]CAACAATCACTTCTT | 7525 |
rs564840172 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:728161 | GGCAACATGGTGAGA[A/C]CCTGTCTCTACAAAA | 7525 |
rs564932454 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:734189 | GAGGCTGAGGCAGGA[C/G]AATTGCTTGAACCTG | 7525 |
rs564946181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:733500 | TAAAAAGCATGGCTT[C/T]CGGCCGGGCGCGGTG | 7525 |
rs564967401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:727772 | TATACATTATAAATT[C/T]GGTAAGATTTTTTAT | 7525 |
rs564971016 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:767032 | CGGAAAATTCTTCAC[C/G]AGAAGATTTTCTACA | 7525 |
rs565047349 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | YES1 | GRCh38.p7 | 18:795946 | ACACACACACACACA[C/T]AAGACCTATGAGTAA | 7525 |
rs565064453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:752408 | AGCCACTGTGCCCAG[C/T]CAACAAATTTAATTT | 7525 |
rs565137960 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:795397 | TGGTAAATCTGGGTG[C/G/T]AGGGTATCCAGTTCT | 7525 |
rs565152807 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:802358 | GGATCACCTGAGGTC[A/G]GGAGTTCCAGACCAG | 7525 |
rs565154630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:753510 | TTTCTTTTTTGAGAC[A/G]GAGTCTTGCTCTGTT | 7525 |
rs565172301 | in-del | -/TC | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:764737 | TGAATCTTTCTTTTT[-/TC]TCTCTTTTTTTTGAG | 7525 |
rs565192702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:739473 | CTGGGAATGGTGGCC[C/T]GTGCCTGCAGTCCTA | 7525 |
rs565207580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:729401 | GCCTGGGAGACAGAG[C/T]GAGACTCTGTCCCAA | 7525 |
rs565207617 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:751635 | CTGGATCATCAACCA[C/G]CTCAGTGGTTCCTGT | 7525 |
rs565209765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:757367 | AATTAGCCGGGCGTG[A/G]TGGTGGGCGCCTGTA | 7525 |
rs565221226 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:789608 | AAAAACCCCCAAAAC[-/A]AAAAAAACCCAACAA | 7525 |
rs565252457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775231 | CGAATGTTTGCAACT[A/G]TGATCATTTTGATAA | 7525 |
rs565255009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:768650 | TGGTCCCGTAAGATT[A/G]TAATACTGTATTTTT | 7525 |
rs565264300 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:799899 | CAAAACAAACAAACA[A/G]AAACAAAAAACAAAA | 7525 |
rs565279210 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:740040 | AAGAAAATGCATTAA[C/T]TTTACCTGACAAGAG | 7525 |
rs565351672 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:769716 | ATGTAGTGAATTTTA[C/T]TAATTGATTATTGAC | 7525 |
rs565389594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:774525 | TTAACGCCATTCTTC[C/T]AGTTTTTCAGGCCCA | 7525 |
rs565389883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:782231 | GCACAATGGCCTTTT[C/T]GGCTCTTCATAAGGT | 7525 |
rs565396817 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:735611 | CCCAGCTACTCGGGA[C/G]GCTGGGGCAGGAGAA | 7525 |
rs565431637 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:764101 | CTCCAGCCTGGGCGA[C/G]AGAGCGAGACTCCCT | 7525 |
rs565452089 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:809567 | CTGCCTCCTAAAGTG[C/T]TGGGATTACAGGTGT | 7525 |
rs565455658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:802881 | TGAGCCCAGGAGTTC[A/G]AGACAGCCTGGGCAA | 7525 |
rs565481196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:763867 | TGGCTCACATCTGTA[A/G]TCCCAGCACTTTGGG | 7525 |
rs565501026 | in-del | -/TTAA | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:726048 | TTTATGCTTATTATT[-/TTAA]TTGACTGTTAGGATT | 7525 |
rs565522812 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723079 | CCTGGGCGACAGAGC[A/G]AGACTCCGTCTCAAA | 7525 |
rs565554930 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | YES1 | GRCh38.p7 | 18:749802 | GGGGCAGAGCTTGCA[A/G]TGAGCCGAGATTGCG | 7525 |
rs565599403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:730501 | AGGAGTGAGTCACCA[C/T]GCCCAACTGGAATTT | 7525 |
rs565629278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:770267 | CGCCCGGCCCTTTTA[C/T]CTTTTTTTTTTTTTT | 7525 |
rs565636877 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:738981 | GGCGCCCGCCACCAC[A/G]CCTGGCTAATTTTCA | 7525 |
rs565669065 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:810804 | AAAACCAAAAAACCA[C/T]ATATATTATTTGCTA | 7525 |
rs565678522 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:754990 | AATACCCCTAATAGA[A/G]TATTTCATATAAGTA | 7525 |
rs565679700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:804424 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCCAT | 7525 |
rs565684907 | snp | C/T | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724290 | AGTGGTTTTGTGCAA[C/T]CATATCTGGGATTCC | 7525 |
rs565697035 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:727959 | ACCAGAAGTGTTTCC[A/G]ATTTTGGATTTTTTT | 7525 |
rs565705597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:724899 | AACCCCATTTGATTA[A/G]TAAGAATTTAGGGTG | 7525 |
rs565725360 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:783297 | GAAAATATCTCAAAT[A/G]TACATTTAAAAACTC | 7525 |
rs565738546 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:771219 | TAAAAATACAAAAAT[A/C]AGCTGGGCATGGTGG | 7525 |
rs565762069 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:781137 | AACTGGGAGTGGTGG[C/T]AGGCACCTATAATCC | 7525 |
rs565768971 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776703 | TTCAGATCCTAATCA[C/T]ACCCGTTTCTACAAT | 7525 |
rs565794716 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:747298 | AATAGGCGAAACCCC[A/G]TCTCTACTAAAAATA | 7525 |
rs565797220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:784906 | TATATTCAAAGGTTC[C/T]GAGAATTCACAGAAC | 7525 |
rs565800585 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:735617 | TACTCGGGAGGCTGG[A/G]GCAGGAGAATCGCTT | 7525 |
rs565843582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:799077 | AGTCCGTTGGACTAA[C/T]CAGTTTGCTTTATAC | 7525 |
rs565859735 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:804432 | GCCAACATGGTGAAA[-/C]CCCCCATCTCTACTA | 7525 |
rs565860886 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | YES1 | GRCh38.p7 | 18:777803 | CAGAGTGAGACTCTG[A/G]CTTAAAAAAAAAAAA | 7525 |
rs565905802 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | YES1 | GRCh38.p7 | 18:792870 | AGCCAAGGGGGGGGA[A/G]AAAGCTTAAATCAAC | 7525 |
rs565927254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:743692 | GCAGATGAATCACGA[A/G]GTCAGGAGTTCGAGA | 7525 |
rs565927731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:806117 | ACTTCTTTTTCTTTT[C/T]GTCCTAGGTATATAT | 7525 |
rs565934525 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | YES1 | GRCh38.p7 | 18:806504 | AAAGATTTGTTTTGT[C/T]TGCGAAAAGTCCATA | 7525 |
rs565943610 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:800982 | GAAACTCCGTCTCTA[C/T]TAAAAATATAAAAAT | 7525 |
rs565945756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:805033 | TCAGTTTTTTATAAT[C/T]TTTACTTATATCTAA | 7525 |
rs565991105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:793329 | CAGGCGTGAGCCACC[A/G]CGCCTGGCCATTATA | 7525 |
rs566025705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:755159 | GTATTCAGAATTAGG[A/G]GGCTGGAATTAAGAC | 7525 |
rs566071306 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:749577 | TGTTATCTAGAAGGC[C/T]GGGCGCGGTGGCTCA | 7525 |
rs566106260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:766453 | AGCACTACATGATTA[A/G]TGAAAGATGATTATC | 7525 |
rs566140434 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:793377 | GGTTTCACTCTGTCA[C/T]CCAGGCTACAGTGCA | 7525 |
rs566157548 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:781927 | GTAGCTTAAGCAAAA[A/G]GGGGATTTTTTATAA | 7525 |
rs566201648 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:789047 | ACATTATTAGTTTGA[A/G]AATGGATATTTTAAA | 7525 |
rs566241341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:781402 | ACCTCCCTCTTTCCT[C/T]ACGCTTGGCTTGTGA | 7525 |
rs566243282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:789447 | AATTAGCCAAGTGTG[A/G]TAGTACAGGCCTGTA | 7525 |
rs566248283 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:760556 | GTTATATACAAATAC[A/G]TGCCATTTTATATCA | 7525 |
rs566263419 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:748135 | TTCATTTTTTATTTA[C/T]GCATTCATTGGATGA | 7525 |
rs566274956 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:732571 | AAGAGGCCCCTTTGG[A/C]AAATGTCCTGAGAAA | 7525 |
rs566293987 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721470 | GTGACCCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 7525 |
rs566320999 | snp | C/T | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812773 | GCCAGGGCTTTGGGG[C/T]TTGCTTTTGTGGGGG | 7525 |
rs566321130 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:808605 | GATCTTACTAAAACT[G/T]CCTGTAAATATTCAC | 7525 |
rs566335962 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:732001 | AAGTCTCTTAATTTT[G/T]AAAGGGAAACACTTT | 7525 |
rs566361231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:772204 | CCAGCTAATTTTGTA[C/T]TTTCAGTACAGACAG | 7525 |
rs566393994 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:811935 | GGTAGCGCGGGGAAC[C/G]AGACAAGCCCGCCGG | 7525 |
rs566460872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:739150 | TATTTTCTAAGAAAC[C/T]GTATGATACAGGACA | 7525 |
rs566471693 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:745539 | CTGAGTAGCACAATG[A/C]AAGTACTAAGTATTA | 7525 |
rs566497994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:739659 | TCACTACACATACTA[C/T]AATATTCTGGTAAGA | 7525 |
rs566523303 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:796181 | GAAAACAGGAAATTT[G/T]TCCTTCTAGGAATCA | 7525 |
rs566525412 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:763666 | CTGTGATCGTGCCAC[G/T]GCACTCCATCCTGGA | 7525 |
rs566546180 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:729097 | CTTTTCACTATGCCC[A/C]ACTGGTTTCATACAT | 7525 |
rs566564379 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:731954 | CCTGGGCGACAGAGC[C/G]AGACTCCATTTCAAA | 7525 |
rs566585837 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722952 | AAAAAACTAGCCAGG[C/T]GTGGTGGTGGGCACC | 7525 |
rs566589728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:803213 | TCATTCCAGCCTGGG[C/T]GTCAGAGTGAGACTC | 7525 |
rs566622519 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:769250 | AAGTGACGTGCGACC[C/G]TAAGTAAATCTGTAT | 7525 |
rs566641394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:774662 | CCCACTGCTACCCTG[A/G]TCTAGGTCACATCAC | 7525 |
rs566707951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:753715 | GGTCTCAAACTCCTG[A/G]CCTCAAGTGATCTAC | 7525 |
rs566734408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:734285 | CTTGGCCAGGCGCGG[C/T]GGCTCACGCCTGTAT | 7525 |
rs566745597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:741842 | AAACAAACAAAAAAA[C/T]GTCATATTTGGCAAC | 7525 |
rs566767624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:746948 | TTTTTTCTTAACTAA[C/T]TGTAAGTTGCAAACA | 7525 |
rs566802564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:790576 | AACACAAAGGGAGAG[C/T]ACACAGTATTAGGTA | 7525 |
rs566806270 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:730502 | GGAGTGAGTCACCAC[A/G]CCCAACTGGAATTTT | 7525 |
rs566823959 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:758614 | TGATGGTCATCACAA[A/T]TGTTACTTTTCCATT | 7525 |
rs566906446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:797614 | GACAAGGTAGTTCAA[C/T]AAAGCACTTCTAAAC | 7525 |
rs566912826 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721430 | GTAGTCCCAGCTACT[C/T]GGGTGGCCGAGGCAG | 7525 |
rs566929055 | snp | A/C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723040 | GAGCTTGCAGTGAGC[A/C/T]GAGATCGCGCCACTG | 7525 |
rs566952232 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:763953 | GGCGAAAACCCGTTT[C/G]TACAAAAAATAGAAA | 7525 |
rs566976238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:726381 | AGTGAGCTGAGATCG[C/T]ACCACTGCACTCCAG | 7525 |
rs567032364 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:794963 | TCGAACTACAGGCGC[A/G]TGCCACCATGCCTGG | 7525 |
rs567096912 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:783904 | CAGGTGTGAACCACC[A/G]CACCTAGCTCATTAA | 7525 |
rs567097012 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776225 | TTGAGATGGAGTCTC[C/T]CTCTGTCGCCCAGGC | 7525 |
rs567112269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:744431 | GTCTCACTCTGTCGC[C/T]CAGGATGGAGTGCAG | 7525 |
rs567124556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:744872 | AGTCAGGGAACCCTA[A/G]ATTCATAACAGCTTG | 7525 |
rs567166361 | snp | A/G | 0.000217824 | 0.0104338 | intron-variant | YES1 | GRCh38.p7 | 18:756863 | TAAAATATTTTGAGA[A/G]TCAGTTAACACACAG | 7525 |
rs567180506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:747399 | GCTTGAGCCTGGGAG[A/G]TAGAGGTTGCAGTGA | 7525 |
rs567197238 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:800353 | ACTAAGATCCCTACC[C/T]TCACGGAGCTTACAT | 7525 |
rs567206836 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:756349 | ACATGATCCAGTACA[A/T]AATCACCATCAGGTT | 7525 |
rs567222808 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:761342 | ATATCAAGAAAACAG[A/C]ATTAATTATTACATA | 7525 |
rs567239384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:799738 | AATAAAAAACACAAA[C/T]ACAAATACAAAAATT | 7525 |
rs567266410 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:749679 | GCTAACACGGTGAAA[A/C]CCCGTCTCTACTAAA | 7525 |
rs567349077 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:765754 | AACAGACTTTCAGGA[A/C]GAAAATGGCTAATAG | 7525 |
rs567350217 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:730249 | CTCTGAACTCTGCTC[A/G]ACTCCCCAGCCTCCT | 7525 |
rs567367481 | snp | A/C | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722781 | AGGGAAAAAATGACC[A/C]CCATTACATAGACTT | 7525 |
rs567384254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:738378 | ATACCATCTTAATTC[C/T]TGTGTTGGACTATAG | 7525 |
rs567408339 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:760431 | GTCAAGATTATGCCA[C/T]TGCACTCCAGCCTGG | 7525 |
rs567409199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:794136 | GTGGTGATGAAACCT[A/G]ACAGATATCACTTAA | 7525 |
rs567471495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:757331 | ACACGGTGAAACCCC[A/G]CCTCTACTAAAAATG | 7525 |
rs567475232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:750171 | TTAATAATTCAAATA[C/T]TTAGAAACTCATACA | 7525 |
rs567480739 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:779800 | GATACCACTTTCAAG[C/T]CCTTATGTCAATTAA | 7525 |
rs567513111 | in-del | -/AA | 0.46885 | 0.12085 | intron-variant | YES1 | GRCh38.p7 | 18:730959 | AGAGAAGGGTGAAAT[-/AA]CAGCAAAGGAGTGAT | 7525 |
rs567519218 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:785585 | ATGGTTTGAATATGC[A/C]CCCAAAGTTCACGTG | 7525 |
rs567521595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:767295 | GCTGGGACTATAGGC[A/G]AGCACCACCACGCCT | 7525 |
rs567566182 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:727931 | TGAGTATCCCTTATC[G/T]GAAATGTTTGGGACC | 7525 |
rs567594829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:762197 | TGGTGGCCCATGCCT[A/G]TAATCTCAGCTACTC | 7525 |
rs567598394 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | YES1 | GRCh38.p7 | 18:768177 | AAGTGTGGCAATGTT[-/A]AAAAAACCATTTCCA | 7525 |
rs567660436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:773349 | CTTCCTGGATAACGG[A/G]CAAGAGAAGGCAGAG | 7525 |
rs567662097 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813154 | AGTGCAACAAGTATG[G/T]TTCTCCTGCTTGTCA | 7525 |
rs567673925 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813869 | CGTGTAACCCCAGCA[C/T]TCTGGGAGTCCAAGA | 7525 |
rs567674084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:807440 | AGAGGTCAAGGCTGC[A/G]GTGAGCTGTGACTGC | 7525 |
rs567674650 | in-del | -/A | 0.00914312 | 0.0669923 | intron-variant | YES1 | GRCh38.p7 | 18:792869 | AAGCCAAGGGGGGGG[-/A]AAAAGCTTAAATCAA | 7525 |
rs567686481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:770194 | TGATCTCCTGACGTC[A/G]TGATCTGCCTGCCTC | 7525 |
rs567746765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:801515 | AAATGGCTATCTTTC[C/T]GCAACACGTCTGAAA | 7525 |
rs567777835 | snp | A/C | 3.33011e-05 | 0.00408038 | intron-variant | YES1 | GRCh38.p7 | 18:751824 | CAGAGGGAAAAAAGA[A/C]CAAGGTAAATTATGT | 7525 |
rs567812319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:795672 | AGAAAACCAAACACC[A/G]TATGTTCTCACTTAT | 7525 |
rs567819509 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:769489 | GAGAGAATATCTATG[C/T]CTTGGTTCTCAATCT | 7525 |
rs567901639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:728373 | CTTATACATATAGCC[C/T]GAAGGTAATTTTACA | 7525 |
rs567932722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:807914 | TTAAAGTGAAATGAA[A/G]TATAATGCTTCAAGG | 7525 |
rs567939117 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:729815 | TATTTTTAGCAGAGA[A/T]GGGGTTTTACCATCT | 7525 |
rs567988979 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:757302 | AGGTCAGGAGATTGA[A/G]ACCATCCTGGCTAAC | 7525 |
rs567990970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:764379 | AGGCATGTGCCACCA[C/T]GCCCGGCTAATTTTG | 7525 |
rs568026173 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:735013 | AATACAAAAATTAGC[C/T]GGGCCTGGTGGCAGG | 7525 |
rs568055002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:764795 | TGGAGTGCAGTGGCG[C/T]GATCTCGACTCACTG | 7525 |
rs568069312 | in-del | -/AC | | | intron-variant | YES1 | GRCh38.p7 | 18:783393 | TTATGTAGGGGAAAC[-/AC]ACACACACACACACA | 7525 |
rs568133526 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | YES1 | GRCh38.p7 | 18:757288 | GCGGGCGGATCACGA[G/T]GTCAGGAGATTGAGA | 7525 |
rs568148089 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:797765 | ACGTTCACCTTTTAA[A/G]ACATCATCTAATCAT | 7525 |
rs568151270 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776175 | ACCATTGCTTTACAT[C/T]ATCAATACTTGGTAT | 7525 |
rs568200201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:759341 | GCGAGGTGGCGGGCG[C/T]CTGTAATTCCAGCTA | 7525 |
rs568218851 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:750250 | CCAAAAACCTTGTAT[C/T]TGATCCTGCTAAGCA | 7525 |
rs568231498 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:784082 | ATTCATTTTAACACA[C/T]ATGTTGTCATACATA | 7525 |
rs568231944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:804326 | TTACGAAAAAATCTG[A/G]GCTAGGCACAGTGGC | 7525 |
rs568235743 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:792803 | TTGTCTTTATTTTTT[A/T]AAAAAATGTAAAAAA | 7525 |
rs568249458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:724714 | CCCCTAGCCACTAAC[C/T]CATTCAAAGTATATT | 7525 |
rs568260423 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:754902 | TGTAAGCTCCATCAG[A/G]ACAGAAACTTTGTCT | 7525 |
rs568281858 | in-del | -/AG | | | intron-variant | YES1 | GRCh38.p7 | 18:747686 | AAGTGAAAACATAAA[-/AG]AGAGAGACTAGGCAT | 7525 |
rs568283900 | snp | C/T | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:777001 | GAAAAACAAAAAGGC[C/T]AATTAGACATTAACC | 7525 |
rs568315983 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | YES1 | GRCh38.p7 | 18:759422 | CAGTGAGCCAAGATT[A/G]TGCCATTGCACTCCA | 7525 |
rs568326536 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:811808 | GCCGGGCGGTCCACA[C/G]GACCCCAAAGACAAG | 7525 |
rs568398912 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:774477 | TCCTCCCCAAAGCAG[C/G]TCCTCCTGCAATCTT | 7525 |
rs568425654 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:748684 | TACTTGGCATAATTT[C/T]TTAAAGGTTCATCTA | 7525 |
rs568457621 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | YES1 | GRCh38.p7 | 18:744792 | TCCTGCATCAGTAGT[C/T]GGGATTAAAGGCACA | 7525 |
rs568493487 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:783858 | ACATCAGGTGATCCA[C/T]CTGGCTCAGCCTCCC | 7525 |
rs568509777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:755384 | CTCCCGAGTAGCTGG[A/G]ACTACAGGTGCGCAA | 7525 |
rs568543358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:788294 | GGGGAGCCTTTTAGC[A/G]TGGGCTATAAAATGA | 7525 |
rs568569838 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:794960 | TGCTCGAACTACAGG[C/T]GCGTGCCACCATGCC | 7525 |
rs568614794 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:731722 | CCTGTAATCCCAGCA[C/T]TCTGGGAGGCCGAGG | 7525 |
rs568618515 | snp | C/T | 0.000922069 | 0.0214519 | synonymous-codon | YES1 | GRCh38.p7 | 18:747982 | ATAACCATTCTTTCC[C/T]GTAGCGATTGATCTT | 7525 |
rs568628692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:787507 | TGAAGGTCAGGAGTT[C/T]GAGACCAACCTGGCC | 7525 |
rs568633081 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:781364 | TCAAATGTACCATAC[C/T]GTTTTCATAAACGCT | 7525 |
rs568638148 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:765121 | CAATGTTGGAGGACA[A/C]CTACATACAAGCATA | 7525 |
rs568670963 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:758911 | AGCACTAATATAGAA[C/T]TCATTAATTCACTTA | 7525 |
rs568729155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:728707 | ATTTTTGTATTTTTA[A/G]TAGAGATGGGGTTTC | 7525 |
rs568742372 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:771468 | ATTTATTCCTTAAAA[A/C]TCACCTTCAAATAAA | 7525 |
rs568753268 | in-del | -/TTA | | | intron-variant | YES1 | GRCh38.p7 | 18:790479 | TCTTTTAATTTCCTC[-/TTA]TTATAACAAAAAATC | 7525 |
rs568831791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:745054 | TGCTGGCTGACTTGA[C/T]AGACTCAGTTTGCAG | 7525 |
rs568838399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:738543 | AAAATACAAAAGATT[A/G]GCTGGGGGTGGTGGT | 7525 |
rs568865046 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:780594 | AATTCCTTTTCTTTA[C/T]AAATTAGCCAGTTTC | 7525 |
rs568891821 | in-del | -/AT | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813517 | GGAAATAGTGCAATC[-/AT]ATGTGTCAGTATTCC | 7525 |
rs568893255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:745439 | TTTATTTTCATAAGG[C/T]ACATGTGGTGAAATG | 7525 |
rs568904944 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722929 | AACTGCGTCTCTACT[A/G]AAAATACAAAAAACT | 7525 |
rs568913076 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:727182 | TTACATAGCTCATTT[C/T]GGATTTTTGTTTCCC | 7525 |
rs568936373 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:733973 | GGCACCATTACAAAA[G/T]GTTTTATTTAAAAAG | 7525 |
rs568965933 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722878 | CGGGCAGATCACAAG[G/T]TCAGGAGATCGAGAC | 7525 |
rs569038954 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:767978 | AGTGATGGAATTACA[C/G]GCATGAGCCACTGTG | 7525 |
rs569040072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:808128 | TTTCAGATCTTAAAG[A/G]TAAACCCAACGCAGA | 7525 |
rs569050204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:734211 | TTGAACCTGGGGGGC[A/G]GAGGTTGCAGTGAGC | 7525 |
rs569050360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:781361 | TCCTCAAATGTACCA[C/T]ACTGTTTTCATAAAC | 7525 |
rs569061008 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:774150 | CATCTGCTTTGTAAG[A/T]CATTACCCTCTTGGT | 7525 |
rs569066635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:774629 | ATACATTCAGTATCT[A/G]ACAACTTCTCTCCAC | 7525 |
rs569071351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:746855 | CAACTAGGTTCCCCA[A/G]TGGCTAACATTTTGC | 7525 |
rs569097485 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:739083 | ACCCACCTCGGCCTC[C/T]CAAAGTGCTCAGATT | 7525 |
rs569110252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:740540 | GGACTGGTCCAGAGC[C/T]AGGGAGACCAAATTC | 7525 |
rs569130367 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:757469 | GATCGCGCCACTGCA[C/G]TCCAGCCTGGGCGAC | 7525 |
rs569140679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:802294 | AAAGTATTGCCAGGC[A/G]TGGTGGCTCATGCCT | 7525 |
rs569223343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:808585 | TAGGGTTCTAAACAA[C/T]GGAAGATCTTACTAA | 7525 |
rs569258243 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:746393 | CTATGACAGGAAGAA[C/T]AGAAGTGGTTCCCTG | 7525 |
rs569264257 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722899 | AGATCGAGACTATCC[C/T]GGCTAACACGGTGAA | 7525 |
rs569280255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:802998 | TTTGGGAGGCCGAGG[C/T]GGGAGGATCCCTTGA | 7525 |
rs569318655 | snp | A/G | | | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721463 | GAATGGCGTGACCCC[A/G]GGAGGCGGAGCTTGC | 7525 |
rs569319353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:796400 | GGGACTGTCACACAG[C/T]CAATTATCAATACAC | 7525 |
rs569367657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:731699 | GAGGCCAGGCACGGT[A/G]GCTCACGCCTGTAAT | 7525 |
rs569371016 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:763181 | GCTGGGTAGGACAGG[A/C]AGCTAGAGGAGATTT | 7525 |
rs569383359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:763648 | GGTCAAGGCTGCAGT[A/G]AGCTGTGATCGTGCC | 7525 |
rs569420932 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:741350 | CTGGGCTCAAGCAAT[A/C]CTCATGCCTCAGCCT | 7525 |
rs569437728 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:752937 | GACACAGCAAGACTC[C/T]GTATCAAAAAAATAA | 7525 |
rs569470958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:749631 | GAGACCGAGGCAGGC[A/G]GATCACAAGGTCAGG | 7525 |
rs569513228 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:802154 | GTAGTCTTAGCTGCT[C/T]AGGAGGATTACTTGT | 7525 |
rs569519036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:757919 | AAAAAAAGAGAAAAA[C/T]CTACCTCATAAGGTT | 7525 |
rs569526237 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:789881 | TCTGATCAACGTGGT[A/G]AAACCCCGTCTCTAT | 7525 |
rs569530420 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:796852 | CAAACACTAAAAGGT[A/G]GCATTTTGAACCAGT | 7525 |
rs569554560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:805985 | CAATCTTGAAGTTTC[A/G]GGGGTCAGTACTTTT | 7525 |
rs569584543 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:753619 | GCGTCCTGAGTAGCT[C/G]GGATTACAGGCGTGC | 7525 |
rs569586639 | in-del | -/T | 0.391024 | 0.206427 | intron-variant | YES1 | GRCh38.p7 | 18:730344 | AAGGACCCAAGAGGA[-/T]TTTTTTTTTTTTTTT | 7525 |
rs569587877 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:790436 | TCATACTGAGATTTC[C/T]GTTTCTCGTTTCTAA | 7525 |
rs569589625 | in-del | -/ACTC | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:781419 | GCTTGGCTTGTGACT[-/ACTC]ACTCAACCTTCAGGT | 7525 |
rs569600981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:755620 | AGTCTATGCTTGTAG[C/T]GGGGATTTATCTTTT | 7525 |
rs569601764 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:762261 | GGAGGCAGAGGCTGC[A/G]GTGAGCCGAGATTGC | 7525 |
rs569608492 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:759851 | TCTCCTAATGCTATC[A/C]TTCCCCCCTCCCCCC | 7525 |
rs569616670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:805184 | TAGAGTGTACTTACA[C/T]AAACCTACGTGGTAT | 7525 |
rs569644610 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:764837 | TCCTGGGTTCATGCG[A/G]TTCTCCTGCCTCAGC | 7525 |
rs569660497 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:756283 | CCCGGTGCCTACAGT[A/G]GGGGGGGGCTCAATA | 7525 |
rs569662762 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:748887 | ATTTCTGGGCCAGGC[A/G]TAGTGGCTCAAGCCT | 7525 |
rs569697667 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:808076 | CATTATTCTATACTC[C/T]AAAATTACAGGATTC | 7525 |
rs569704151 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:811376 | GTCCCTACACCAGAC[A/T]TGATTTTCAAAGAGC | 7525 |
rs569736307 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:805859 | AATTTCTACTTAATG[C/T]TAAGAAACTGAAAAG | 7525 |
rs569746386 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:744073 | AACTTAAAATATATA[-/T]TTTTTTAAGTTATTA | 7525 |
rs569762088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:771392 | AAAAATTCATTTGAG[C/T]GCAGAGGGTATTATT | 7525 |
rs569821771 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721353 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT | 7525 |
rs569824972 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:800471 | CTGTTAGAGTTAACA[C/T]GTGAAGGAGTTGTAC | 7525 |
rs569831960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:760385 | TGAGGCAGAAGAATC[A/G]CTTGAATCTGGGAGG | 7525 |
rs569836306 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:772257 | TGGTCTCAAACTCCC[A/C]ACCTCAAGTGATCCT | 7525 |
rs569847198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:793421 | CGCTCACTACAGCTT[C/T]GAACTCCTGGTCTGA | 7525 |
rs569848110 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:744271 | GCCTTTGTACACTGG[A/G]TTTTATTAATTCTCA | 7525 |
rs569851260 | snp | A/C/G | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723052 | AGCCGAGATCGCGCC[A/C/G]CTGCACTCCAGCCTG | 7525 |
rs569853486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:743783 | TGGTGGTGCATGCCT[A/G]TAGTCTCAGCTACTA | 7525 |
rs569899645 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:800500 | ACTGTAGATATTGTG[G/T]GATAATAATGCTACA | 7525 |
rs569923145 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:792978 | TCAAGTCAACTTTGG[C/T]ATCACAGCTTAATGG | 7525 |
rs569929152 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:737785 | CGTGCAGTGGTGCAA[C/T]CGTGGCTCACTGCAA | 7525 |
rs569933538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:799680 | TGCATTCCAGCCTGG[A/G]CAACAGAGCGAGACT | 7525 |
rs570009904 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:786033 | AAGGCCCTTGCCAGA[A/T]GTCAGCACTTTGGTA | 7525 |
rs570010122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:766483 | CTTTTCTATGTTTTC[A/G]TATTTATGGAAGTAT | 7525 |
rs570070967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:779652 | TATGTATCATTCCCT[C/T]TACAAATCCAGTCAA | 7525 |
rs570205636 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:757182 | TGATTTCAGGGTATG[C/T]TGCTTAACCTCTATG | 7525 |
rs570227021 | in-del | -/TG | 0.144605 | 0.226698 | intron-variant | YES1 | GRCh38.p7 | 18:792573 | CTGTATATGTGTGTG[-/TG]TGTGTGTGTGTGTAT | 7525 |
rs570291622 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722617 | GCTATTCAAATCTGT[A/G]TTTTGAAATTACTGA | 7525 |
rs570318876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:727038 | AAGAAAGACAATGAA[C/T]GATAAAGTATCTCTT | 7525 |
rs570336096 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813090 | GTGGCTTTGGCTTAT[G/T]TTGGGACAGCGTTTT | 7525 |
rs570337901 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:772440 | TCTATTTCTTTTTTC[-/T]TTTTTTTTTGAGATA | 7525 |
rs570339218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:761639 | TATGCTTAACCTGTC[C/T]TCCAGCCTCATTTTC | 7525 |
rs570410752 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:782042 | TTCTCTGTTTCTCCT[C/G]GTCTTTCCATCACTT | 7525 |
rs570425610 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:770106 | CTGGCAGTACAGGCA[C/G/T]GCGCCACCACACCCA | 7525 |
rs570442547 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:734312 | GTATTCCCAGCACTT[C/T]GGGAGGCCGAGGTGG | 7525 |
rs570496446 | snp | A/G/T | 3.41217e-05 | 0.00413036 | missense | YES1 | GRCh38.p7 | 18:739781 | TTCAAATACTTTCCA[A/G/T]CTCCTTCCTTAAGGA | 7525 |
rs570525589 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:758213 | ATTTTAATGACATTT[G/T]ATTTTTTCATACTGA | 7525 |
rs570570626 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:754533 | CAACGTGGTGAAACC[C/G]CGTCTCTACTAAAGT | 7525 |
rs570580429 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:797696 | ACATCTTTTTAACAA[A/T]CTTTAAAAATTTTGT | 7525 |
rs570595824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:764292 | CAATGGTACAATCCC[A/G]GCACACTACAACCTC | 7525 |
rs570601621 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:731838 | TGGGCGTGGTGGCGG[A/G]TGCCTATAGTCCTAG | 7525 |
rs570659122 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723487 | GTCCCTGATCTGGTC[A/G]TATTTTCTATTTGTG | 7525 |
rs570662629 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:763989 | AGCGGGGTGTGGTGG[C/T]GGGCACTGTAGTCCC | 7525 |
rs570718367 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:729730 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 7525 |
rs570727601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:730974 | TCAGCAAAGGAGTGA[C/T]TATACTGCTTCACTA | 7525 |
rs570762441 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:741283 | AGTCTCATTTTTTCA[C/G]CCCAGATGGGAGTGC | 7525 |
rs570774088 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:793291 | TGATCCACCCACCTC[A/G]GCCTCCCAAAGTGCT | 7525 |
rs570816542 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:754775 | AGCTTTCCCTGATTA[A/T]CTGCAGGGCCTTCAC | 7525 |
rs570818530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:747425 | AGTGAGCCGAGATCA[C/T]GCCACTGCACTCTAG | 7525 |
rs570879298 | snp | C/T | 0.000166276 | 0.00911649 | intron-variant | YES1 | GRCh38.p7 | 18:747890 | TTTCAAAAATCAAAA[C/T]AATTAATAAAATATG | 7525 |
rs570888142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:800939 | GATCACGAGGTCAGG[A/G]GATCGAGACCATCCT | 7525 |
rs570912620 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:793143 | CTCCCGGGTTCAAGC[A/G]ATACTCCTGCCTCAG | 7525 |
rs570919806 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:763064 | AAGGATATTCCAGGA[A/C]GAATGAAAAGTGTAC | 7525 |
rs570947718 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:786742 | GATTTGCTGCACATC[A/G]AGTTTTTATATGGTC | 7525 |
rs570964382 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:810842 | ACTTTCTTACTGTAC[A/T]ATATATGAACATCGT | 7525 |
rs570974686 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:735969 | TGAGCCCAGAAGTTC[A/G]AGACCAGCTTGGGCA | 7525 |
rs571006234 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:735629 | TGGGGCAGGAGAATC[G/T]CTTGAATCTGGGAGG | 7525 |
rs571063508 | in-del | -/AA | 0.00438332 | 0.0466095 | intron-variant | YES1 | GRCh38.p7 | 18:725096 | TGAATTACTTCTGTG[-/AA]AGTTTCCTTATCTAA | 7525 |
rs571083799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:784032 | ACAGGCATAATACGA[C/T]GGAATTTCCCCAAAT | 7525 |
rs571087076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:771090 | CAAGTGATGGCTGGG[C/T]ATGGTGGCTCATGCC | 7525 |
rs571126992 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:733364 | GTTTATGGGTTTTCC[A/T]ACTTTTTATATCATT | 7525 |
rs571146563 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:764870 | CCCGAGTAGCTGGGA[C/T]TACAGGTGCACACCA | 7525 |
rs571165239 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:742002 | TTCCTACAGCAAATA[C/T]GTAACTTGTAGTTGT | 7525 |
rs571194606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:794936 | TTCTCCTGCCTCAGC[C/T]TCCCAAGTTGCTCGA | 7525 |
rs571240064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:744513 | TCCTGCCTCAGCCTC[C/T]CAAGTAGCTGAGCCT | 7525 |
rs571268611 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:786366 | GAGCTTCACATAAGA[C/G]TGTCAAGTTTGAGGG | 7525 |
rs571282508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:751165 | TATTTTGAGAAGTTA[C/T]AAAGTGGTCATTATG | 7525 |
rs571331504 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:743123 | AACACATTTTAGGAA[C/T]TTATATTTTAAAGGA | 7525 |
rs571343967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:761405 | AGGAGGAAAAATTAT[A/G]GGGGAAACCCAGTAA | 7525 |
rs571365645 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:733726 | AGGCGGAGCTTGCAG[A/T]GAGCTGAGATTGCGC | 7525 |
rs571389467 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:806977 | TAGTGGTAAAAGTAA[C/G]GACAAGACGCTGCTG | 7525 |
rs571401481 | in-del | -/AACACTTA | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:752616 | AATTATTACATATTT[-/AACACTTA]AACACTTAAAGATAA | 7525 |
rs571408701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:757037 | AGCCCTACTCCAATC[A/G]CTTCATTCTCCAACT | 7525 |
rs571437346 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813332 | AGGTTAATCAAGGTC[A/C]TCATGGACTGAACCT | 7525 |
rs571441303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:738918 | AACCTCCGCCTCCCG[A/G]GTTCAAGCGATTCTC | 7525 |
rs571465431 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:752868 | GAATCGCTTGAAACC[C/T]GGAAGTGGAGGTTGC | 7525 |
rs571501432 | in-del | -/GTT | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:769679 | TAGATTATCATATAG[-/GTT]TTTTTCCTTTATTCA | 7525 |
rs571504339 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:781188 | GCAGAAGAATTGCTT[G/T]AACCTGGGAGATGGA | 7525 |
rs571504499 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:773493 | AGTGTATTCAAAAAC[C/T]TGAACCATGACAGTC | 7525 |
rs571521904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:762951 | TGGAAATACAACAAA[C/T]GTTATCAGCTCTGCT | 7525 |
rs571587262 | snp | C/T | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:780439 | CTTAGCTTAGCACAA[C/T]AGCACACTCAGCCCC | 7525 |
rs571620073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:808507 | AGAAAAGCAGTTGTG[C/T]CTCGCTATAGGACTT | 7525 |
rs571653151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:757440 | CCCGGGAGGCGGAGC[C/T]TGCAGTGAGCAGAGA | 7525 |
rs571660344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:767869 | CAACAACTGGCTAAT[C/T]TTTGTATTTTTAGTA | 7525 |
rs571713804 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:767363 | ACTATGTTGTCCAGG[A/C]TGTTCTGGAACTCGT | 7525 |
rs571765760 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:774092 | CGCCTTGGCCTCCCA[A/G]AGTGCTGGGATTACG | 7525 |
rs571767119 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:746344 | CAGCAAAATAACAGA[C/T]CCTTTCTGTCAGTGA | 7525 |
rs571808218 | snp | A/C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722858 | AGCACTTTGGGAGGC[A/C/T]GAGGCGGGCAGATCA | 7525 |
rs571817040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:758386 | GGAAACACCCCTAAC[A/G]CTCACCAAATTTAAC | 7525 |
rs571835660 | snp | A/G | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722937 | CTCTACTAAAAATAC[A/G]AAAAACTAGCCAGGC | 7525 |
rs571847488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:796228 | GGTATAGGCTCTGGA[A/G]TCACAAAGTTAGGTT | 7525 |
rs571892874 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:763523 | GTCATGGCAGAACCC[C/T]GTCTCTACAAAAAAT | 7525 |
rs571917606 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:753920 | TACCATCTAATCAGG[A/T]ACTCAAGCCGAGTCC | 7525 |
rs571936836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:795715 | AACAATGAGAACACA[C/T]GGACACAGGGAGGGG | 7525 |
rs571957710 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:784322 | CCACTGAAGATATGT[A/G]TTGTTATTATCTCTG | 7525 |
rs572009728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:798001 | TGACAGGGGAAAGCA[C/T]GAACACAGTCCCTCA | 7525 |
rs572050563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:764441 | TTGTCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 7525 |
rs572059357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:804069 | ACCTTAAAAGGCTAA[C/T]CATTTTCCAATGCCA | 7525 |
rs572103851 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | YES1 | GRCh38.p7 | 18:764075 | CAGTGAGCCGAGATC[A/C]CACCACTGCACTCCA | 7525 |
rs572167157 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:777109 | TGTGCAAAAGCTCAT[A/C]AACAAGAGGGAACAA | 7525 |
rs572174563 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:741528 | GCATATTTGGGCTGG[G/T]TGTGGTGGCTCACAC | 7525 |
rs572296450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:799323 | TGCTAGAAACTATTT[C/T]TTCCAGCTCTCCTTA | 7525 |
rs572302694 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:775002 | TGGCAGAACAGTTAA[C/G]AGCATAGAGGTCAGA | 7525 |
rs572328895 | in-del | -/A | 0.00358779 | 0.0422022 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722473 | AAGAATTATATCCTG[-/A]AAATAGAGGGGCCTA | 7525 |
rs572341051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:768837 | CCTCCCGAGTAGCTC[A/G]GATTACAGGCATCTG | 7525 |
rs572349453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:747550 | ATCCCTATCAACACA[C/T]CCTCATATATAAGCT | 7525 |
rs572384169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:771575 | CTTTTTTGTGATGGG[A/G]TTTCACTTTGTCACA | 7525 |
rs572427906 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:725358 | CCTTGTATCTCTTGG[A/T]AACTTTATCAACCAA | 7525 |
rs572439535 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:764895 | ACACCACCACACCCG[A/G]CTAATTTTTTGTGTA | 7525 |
rs572519213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:807758 | ACCACGGATATGCAA[C/T]GTATAGCTAATTCTA | 7525 |
rs572540486 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:748420 | AAATTCCCCCACTTA[A/C]GATGTACAATTCACT | 7525 |
rs572556056 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:794880 | GGAGAGCAGTGGTGC[A/C]ATCTCGGCTCACTGC | 7525 |
rs572642202 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:809835 | AAACGTAGGGCTTAA[C/T]GAATTACACTAAGAC | 7525 |
rs572701238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:802364 | CCTGAGGTCGGGAGT[C/T]CCAGACCAGCCTGAC | 7525 |
rs572735083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:733462 | TTTTTGTGGAGGGCA[C/T]TATGCTAATCACTAT | 7525 |
rs572763063 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722829 | TGGGCGCGGTGGCTC[A/G]CGCCTGTAATCCCAG | 7525 |
rs572795973 | in-del | -/AA | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:764136 | AAAAAAAAAAAAAAG[-/AA]AAAGTCATTCATTCT | 7525 |
rs572804775 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:809446 | CTGGGATTACAGGGG[C/G]GCGCCACCACACCCA | 7525 |
rs572826508 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:808186 | AGTTCCAAGACAACA[C/G]TAGTGCTGCTGCAGC | 7525 |
rs572855605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:773181 | AATTTCCACATTAGA[C/T]TTTTCTTTAATAGAG | 7525 |
rs572866283 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:773561 | GGTAAGACAGTGAGG[A/T]AAGACAGACACCAAG | 7525 |
rs572885133 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:782102 | CCAACTACCTGGTCC[A/C]TCTCTCCACCCCACT | 7525 |
rs573021213 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:738638 | GAGCTTGCAGTGAGC[A/C]GAGATTGCACCACTG | 7525 |
rs573041368 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:757365 | AAAATTAGCCGGGCG[C/T]GGTGGTGGGCGCCTG | 7525 |
rs573081571 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:768222 | GCTTGCTAAGACCTG[C/T]CAAACCATGCATGAG | 7525 |
rs573119435 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:801286 | TGCAGTTAGCAGTGA[G/T]TGTGCAACTGGAGTC | 7525 |
rs573147268 | snp | C/G | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813783 | TCTTCACTAAATAGA[C/G]ATAATTTCGTCTTCC | 7525 |
rs573179425 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:763225 | ATTTGTTATGCAATA[A/G]CTTTTAGACTTTCTC | 7525 |
rs573253654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:742436 | CCAGCCTGGGCAACA[C/T]AGTTGAGACCCCAGT | 7525 |
rs573347725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:789138 | GTTGTTTGGCATTCA[C/T]TGAGTACTGATAACA | 7525 |
rs573355699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:757512 | CGTCTCAAAAAAAAA[A/G]AAAAAAGAAAGAAAA | 7525 |
rs573381620 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:732732 | AGGCAGGGGGACTAT[A/G]AGAAGAAATAAAGGC | 7525 |
rs573418521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | YES1 | GRCh38.p7 | 18:775058 | GAGTCCGTCACTTAC[C/T]AGCTGGGTGAACTTC | 7525 |
rs573481457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:769052 | TGTTACAACTGCCTA[C/T]AGCATTCAGTATAGT | 7525 |
rs573487997 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:737084 | AGAAGGAGATGATGG[G/T]AACAGGGTATAGTCT | 7525 |
rs573494822 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:809490 | CTTTTTAGTAGAGAT[G/T]GGGTTTCACCACGTT | 7525 |
rs573498081 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | YES1 | GRCh38.p7 | 18:763531 | GAACCCCGTCTCTAC[-/A]AAAAAATACAAAAAA | 7525 |
rs573498971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:766470 | GAAAGATGATTATCT[C/T]TTCTATGTTTTCGTA | 7525 |
rs573509810 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:749030 | GCTAGATGCAGCGGC[A/G]TGCACCTGTAGTCCC | 7525 |
rs573516522 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:799910 | ACAAAAACAAAAAAC[-/A]AAAAAAAAAAGAAGG | 7525 |
rs573532132 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:807514 | AAAAACAAAGCAAAA[C/T]ACAAAAACACAAAAG | 7525 |
rs573539985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:782764 | CAGCGGCACAATCTC[A/G]GCTCACTGCAACCTC | 7525 |
rs573564589 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:753606 | TTCTCCTGCCTCAGC[A/G]TCCTGAGTAGCTGGG | 7525 |
rs573600767 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:739303 | TGGATTATCTCTGAC[A/G]TTCCTGCCAGTTCTA | 7525 |
rs573615271 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | YES1 | GRCh38.p7 | 18:757330 | AACACGGTGAAACCC[C/T]GCCTCTACTAAAAAT | 7525 |
rs573617633 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:734790 | CTATGGAAAACAGTA[C/T]GGAAACTCCTTAAAG | 7525 |
rs573624182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:743823 | AGGCAGATGGATCGC[A/G]TGAACCCAGGAGGCA | 7525 |
rs573630501 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:799198 | CAGATGTCTAACTTG[G/T]GTAACTACCATACTT | 7525 |
rs573646854 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:736376 | TACACTGTAGGAGGT[G/T]CAGCAGTATACCTGG | 7525 |
rs573654258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:784489 | TACAACAAATTACCA[C/T]AAATTTAGTGGCTTA | 7525 |
rs573657519 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:755167 | AATTAGGGGGCTGGA[A/G]TTAAGACTGTAATTG | 7525 |
rs573666381 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:793047 | TATTATTATTGGTTT[G/T]TTTTTTTTTTTGAGA | 7525 |
rs573667468 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:761773 | AGTATCAATGCATAG[G/T]ACCCATCATTGCTGC | 7525 |
rs573693339 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:755759 | TAAAGAAATCTGAGT[A/C]CTTGATGACACCATG | 7525 |
rs573717648 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:785048 | TGCTTCCATACTAAG[A/C]AACATAACTGTTAAA | 7525 |
rs573719231 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:748304 | CAACCTAAGACAGAC[A/G/T]ATAGTGAATAAAACA | 7525 |
rs573868315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:779052 | AATTCCTGGAACCTC[A/G]TAGTTTCTTTAATGA | 7525 |
rs573883464 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:786724 | GAACGTATGGGAAAA[C/T]AGGATTTGCTGCACA | 7525 |
rs573894911 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime | YES1 | GRCh38.p7 | 18:812253 | ACGACGGCAGAGCCG[A/G]CCCGGGACGCGTTAC | 7525 |
rs573931126 | in-del | -/C | 0.0295035 | 0.117819 | intron-variant | YES1 | GRCh38.p7 | 18:734699 | AGTAAAAAAAAAAAA[-/C]AATAGATGTTGGTGT | 7525 |
rs573933362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:787644 | TAACCTGGGATGCGG[A/G]GGTTGCAGTGAGCTG | 7525 |
rs573945344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:780031 | CTGAGGTCAGGAGTT[C/T]GAAACCAGCCTGGCC | 7525 |
rs573952225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:800591 | GTACATTCTTAGATA[C/T]AATTGGAGAAATAAA | 7525 |
rs573965909 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:800063 | TCAAACCTTAGTTTC[C/T]CCATCAGACTCAAGT | 7525 |
rs573980012 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:793916 | TAAGATAATCCATAA[A/G]TCACTCTGATAAATA | 7525 |
rs574010685 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:726582 | GTCAGGAGTTTGAGA[A/C]CAGCCTGGCCAACAT | 7525 |
rs574017865 | in-del | -/ATG | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:747127 | TTTTATAATCATAAA[-/ATG]ATAATAAATCTCTGA | 7525 |
rs574081264 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721591 | GACCACAAAGAATGA[A/G]TTCAATAATGTTCTG | 7525 |
rs574089545 | in-del | -/TAGGTATA | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:769111 | CTATACCATATAGCC[-/TAGGTATA]TAGGTATATAGGTAT | 7525 |
rs574106379 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:796636 | GCCGGGCGTGGTGGC[A/G]GGCATCTGTAGTCTC | 7525 |
rs574163768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:794964 | CGAACTACAGGCGCG[C/T]GCCACCATGCCTGGC | 7525 |
rs574187314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:768972 | CCTCCCGAAGTGCTG[A/G]GATACAGGCATGAGC | 7525 |
rs574195031 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:763788 | GTGTATAAGTATAAT[A/T]ATCAAGGTTGTCAGT | 7525 |
rs574238350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:744627 | ACTCCTGACCTCAAG[C/T]GATCTGTCTGTTTCG | 7525 |
rs574269579 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:790952 | TTAATTCAAAAAAAT[A/T]TTTTTTTAAAGTCTA | 7525 |
rs574293074 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:738128 | CATGAACTGGCGTGG[A/C]ATATGCCTGTTGCCT | 7525 |
rs574293939 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:750665 | TTGAGGTTTGCATAG[A/G]GTGCTATGTAAACAC | 7525 |
rs574299163 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:745113 | AAACATCCCCTCTCC[C/T]AGTATTAATCATGTA | 7525 |
rs574314543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:757683 | AAAAATTAGCTGGGC[A/G]TGGTGGTGCACACCT | 7525 |
rs574354783 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:804306 | AAGTCATTTTTCTAA[C/T]TTTATTACGAAAAAA | 7525 |
rs574377415 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:756049 | CTCCTACTTACTATC[C/T]GTGACTTGGGGGAAA | 7525 |
rs574463045 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722985 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 7525 |
rs574484952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:809433 | GCCTCCCAGGTAGCT[A/G]GGATTACAGGGGCGC | 7525 |
rs574499187 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723055 | CGAGATCGCGCCACT[A/G]CACTCCAGCCTGGGC | 7525 |
rs574507201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:810228 | GTCTTACACCATCGG[C/T]TGGTAATATTTCACT | 7525 |
rs574570696 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | YES1 | GRCh38.p7 | 18:729093 | AGACCTTTTCACTAT[A/G]CCCCACTGGTTTCAT | 7525 |
rs574624290 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:729338 | GAGAATCGCTGGAAC[C/T]TGGGAGGCGGAGGCT | 7525 |
rs574636443 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:747139 | AAAATGATAATAAAT[C/G]TCTGAAATATTTCAA | 7525 |
rs574697540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:747465 | CAGAGCCAAGACCCT[A/G]TCTCAAAAAAAAGAA | 7525 |
rs574714783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:753781 | GTGAGCCACCCTGCC[C/T]GGCTGACATCTTTAC | 7525 |
rs574738762 | in-del | -/CT | 0.00517822 | 0.0506191 | intron-variant | YES1 | GRCh38.p7 | 18:799876 | GGCTAAAGAACGAGA[-/CT]CTGTCTCAAAACAAA | 7525 |
rs574760276 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775184 | TACATATATAAAAAA[C/T]ACACCTAACATAGTG | 7525 |
rs574800202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:730634 | ATGCTTTCTGTCTGG[A/G]TTTTACTGCCCTGTG | 7525 |
rs574802308 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:770725 | TTTAGGGATCACAGT[A/C]CTGCACTGCTGTTGT | 7525 |
rs574820142 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:745441 | TATTTTCATAAGGTA[C/T]ATGTGGTGAAATGAA | 7525 |
rs574891181 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776361 | ACCACGCCTGGCCAA[A/T]CTTTTAAAATGTATC | 7525 |
rs574917321 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812914 | TACTCACACCCTCAT[C/T]ACCATCCTGATCGCC | 7525 |
rs575012032 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:749236 | CGGTGGCTTACGCCT[A/G]CAATCCCAGTACTTT | 7525 |
rs575048901 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:759496 | CAAAAACCCATAACC[A/G]GATCTGGAAACTTAA | 7525 |
rs575069637 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:731033 | GAAGGGGGTGAGAAG[C/G]AGGAAAAGGTGGCAG | 7525 |
rs575072988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:728079 | GGTGGCTCGCACCTG[C/T]AATCCCGGCACTTTG | 7525 |
rs575087753 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:760461 | GGTGAAAGAGTGAGA[C/T]TCTGTCTAAAAAAAA | 7525 |
rs575096986 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:738086 | GGATTGCCAACCTCC[A/C]CTACCATAGAGTGTC | 7525 |
rs575134173 | snp | C/T | 0.000399281 | 0.0141238 | missense, intron-variant | YES1 | GRCh38.p7 | 18:732861 | CTCGGCCCTTTGTTA[C/T]TAGTTCTGTTTGCAG | 7525 |
rs575201800 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:788144 | CTTTTTGGAGTGAAA[C/T]AATGAAGTAAAAAAA | 7525 |
rs575204353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:764664 | AATAATATGTTTAAA[A/G]CTCAGAAAAAGATGG | 7525 |
rs575205444 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | YES1 | GRCh38.p7 | 18:786496 | TCATTAATAAGTCCA[C/T]ACACACACACACACA | 7525 |
rs575208946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:752095 | AAAACTCTGTAGACT[C/T]GGAGAAACAAATTTA | 7525 |
rs575217131 | snp | A/C/G | 0.00398564 | 0.0444627 | intron-variant | YES1 | GRCh38.p7 | 18:764880 | TGGGATTACAGGTGC[A/C/G]CACCACCACACCCGG | 7525 |
rs575253095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:779228 | GCAACAAAAGGAGAC[C/T]CCCGTCCCGGCAAAA | 7525 |
rs575303116 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:732757 | AAAGGCCTTTTCCCC[A/G]CTTACAATTCTGTTC | 7525 |
rs575310492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:762383 | AAACCTACCTGTTGG[A/G]TATTACACTGATTAC | 7525 |
rs575317574 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:757369 | TTAGCCGGGCGTGGT[A/G]GTGGGCGCCTGTAGT | 7525 |
rs575323288 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:737250 | TTGAGGTCATGAGTT[C/T]GAGATCAGCCTGGCC | 7525 |
rs575340110 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:773119 | GCTAGTAGAAATACA[C/G]ATTTTAGCAAAATGC | 7525 |
rs575344882 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:807683 | TTCTCAAACGCCAGG[C/G]ATAAAGAAAGAACAA | 7525 |
rs575372127 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:751563 | TGCAACATGCATCTA[C/T]AGAAGCCAATGCATC | 7525 |
rs575396824 | snp | A/G | 4.10029e-05 | 0.00452767 | intron-variant | YES1 | GRCh38.p7 | 18:739845 | TATTCATAAAAAATA[A/G]GCAAATCTTATATTA | 7525 |
rs575429585 | in-del | -/AAC | 0.00438332 | 0.0466095 | intron-variant | YES1 | GRCh38.p7 | 18:760482 | TAAAAAAAACAAACA[-/AAC]AACAACAACAACAAC | 7525 |
rs575464208 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:768414 | TGATCCATGAATGTG[A/G]TATTTTATTTATTTG | 7525 |
rs575527734 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:792062 | TTCTATGCTTTTCTA[C/T]TAAAAAAAATAGTGT | 7525 |
rs575534264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:733391 | CATTCTGGAAAATTT[C/T]ATTGTACTACTTTTA | 7525 |
rs575605269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:747596 | AGTCAAGGCAGGGAA[C/T]GAGGATAATCAGAAG | 7525 |
rs575687834 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:787920 | GTTTTTAAGCTGTGA[A/C]GACTTGATAATGCTC | 7525 |
rs575692291 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:795761 | GGCCTGTTAGGGGGT[C/G]GGGGGAAGGGGAGGG | 7525 |
rs575703329 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:757360 | TGCAAAAAATTAGCC[A/G]GGCGTGGTGGTGGGC | 7525 |
rs575713116 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:734124 | TCTGTACCAAAAATA[A/C]AAAACTTAGCCAGGT | 7525 |
rs575748984 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:788885 | GAACCAAGATCTCTC[C/T]ACTGCACTCCAGCCT | 7525 |
rs575761294 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:743106 | CATGTTCCTAAAGAA[A/G]TAACACATTTTAGGA | 7525 |
rs575780888 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:795217 | CAGTAACTGTACTGC[A/C]GTTGTATAAGAAAAC | 7525 |
rs575794445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:734381 | AATACGGTAAAACCC[C/T]GTCACTACTAAAAAT | 7525 |
rs575801948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:781516 | GCCCCCACACCATTT[A/G]TGACACTGAATTGTC | 7525 |
rs575825468 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:740597 | TCATGAAAACAAAGA[A/G]CAGAACAGTGGGTTT | 7525 |
rs575873447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:739302 | TTGGATTATCTCTGA[C/T]GTTCCTGCCAGTTCT | 7525 |
rs575891759 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:769604 | AGCAAAGTTCCCTTG[C/T]TTGCTGACAGTTTTT | 7525 |
rs575911737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:728845 | CGGATTTTTGAATTA[A/G]GAATGCTCAATCTGC | 7525 |
rs575926678 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:735663 | AAGTTGCAGTGAGCC[A/G]AGATCGTGCCGCTAC | 7525 |
rs576026933 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:804505 | TCCCAGCTACTGAGG[A/C]GGCTGAGGCAGGGAG | 7525 |
rs576036541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:799448 | GGCATGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 7525 |
rs576061174 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:765940 | AGCCATGAAATGAGG[C/T]AATCTTTGGAATATC | 7525 |
rs576086642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:759163 | AGATGTGAGTTAACT[A/G]TAAGCATCAAAATAT | 7525 |
rs576090893 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:791909 | AAAATACAAAAATCA[C/G]CTGGGGGTGTTGGCG | 7525 |
rs576090953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:798502 | CCAAGTTGGAGTGAC[C/T]GATGGGGTAGGGTGG | 7525 |
rs576150623 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | YES1 | GRCh38.p7 | 18:792552 | CTCTCTCTCTCTCTC[C/T]CTCCCTCTGTATATG | 7525 |
rs576151239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:735702 | CTGGGCTGGGCAACA[A/G]AGTGAGACTCCGTCT | 7525 |
rs576188441 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:765461 | TGGAGTGTAGTGGCG[C/T]GATCTTGGCTCAGTG | 7525 |
rs576202196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:777865 | AGAACATACTTTATA[A/G]CAGCATGTTTAGTAA | 7525 |
rs576253192 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:793893 | CTAACAGATTACAAC[C/T]AGTTGACTAAGATAA | 7525 |
rs576300543 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | YES1 | GRCh38.p7 | 18:799930 | AAAAAAGAAGGTATG[A/T]TTGCTGGACATATAT | 7525 |
rs576354174 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | YES1 | GRCh38.p7 | 18:812116 | ACCGGGTCCTTACCT[A/G]TCCTCCGGCCGCGCT | 7525 |
rs576362698 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:774846 | CAAAGCCAAAGTTCC[C/T]ACTATGGCCTTCAAG | 7525 |
rs576366417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:806234 | ATAACTTGGACTTTC[C/T]TCACTAAAATAGTAC | 7525 |
rs576418244 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:760164 | GAATAGTGCAATCTG[G/T]AGACAATTTAAAGCA | 7525 |
rs576425264 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:803808 | TTGTTCAAAGAGCTC[A/G]GCAGTTAACAAAAAC | 7525 |
rs576446348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:771642 | AAGCCTAGACCTCCC[A/G]GTCTCAAACTATCCT | 7525 |
rs576449509 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:804990 | GAACTGCAATTTGCT[G/T]GAGAAAGTTCCGTGT | 7525 |
rs576486079 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:725936 | CAGTGGAAATACAAC[C/T]AGAAGTTGTTGGGTG | 7525 |
rs576487486 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:774447 | CAAATTTAACATTTC[A/C]AAGAAACCTAATCTT | 7525 |
rs576498243 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:748058 | CCGCAAGGTAGACTA[C/T]TGCCCAAGGTACAAT | 7525 |
rs576513511 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:811670 | ACACACCCGCTCCTC[G/T]CCCCGCACAGCTGCT | 7525 |
rs576524307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:726496 | ATTAAATTATTTGAT[A/G]CCAGCTGGGCATGGT | 7525 |
rs576556789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:801888 | CTCTGTTAATCTGGC[A/G]GAACAAACACCTTAT | 7525 |
rs576615326 | snp | A/C | 0.00517822 | 0.0506191 | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721543 | ACTCCGTCTCAAAAA[A/C]AAAACAAAACAAAAC | 7525 |
rs576619049 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:785842 | CTTGGGAGGCTGAAG[A/T]AGGGAGGAACACTTG | 7525 |
rs576651284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:731770 | CAGGAGATCGAGACC[A/G]TCCTGGTTAACACGG | 7525 |
rs576661616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:760717 | AGTTGCTTCTAAAAG[C/T]ATTAGAAAAAATTAA | 7525 |
rs576673688 | snp | C/T | 0.000197723 | 0.00994094 | missense | YES1 | GRCh38.p7 | 18:756569 | CACCTGTTAAACCAG[C/T]AGGATATGAACTTGG | 7525 |
rs576684555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:749752 | GTAGTCCCAGCTACT[C/T]GGGAGGCTTAGGCAG | 7525 |
rs576755020 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | YES1 | GRCh38.p7 | 18:772454 | CTTTTTTTTTGAGAT[-/A]AGAGTCTCACTCTTG | 7525 |
rs576779903 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722895 | CAGGAGATCGAGACT[A/G]TCCTGGCTAACACGG | 7525 |
rs576854204 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:774971 | GACCAAGCATACTCC[A/C]AGCTTATTGTATGTA | 7525 |
rs576883813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:768319 | CCACAAAAATGCCTG[C/T]TGGGATTCTGACTGG | 7525 |
rs576887314 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:728806 | TGGGATTACAGGCCT[C/G]AGCCACTGCGCCCAG | 7525 |
rs576905731 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:809309 | TTCGGAGTATTTGAC[-/T]TTTTTTTTTGGAGAC | 7525 |
rs576971456 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:790118 | CAGTGGCTCATGCCT[A/G]TAATCTCAGCACTTT | 7525 |
rs577000968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:730543 | TTTAGAGTTCTTTCC[C/T]TATGGTTCCTTCTCT | 7525 |
rs577083361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:753269 | AGTAGAGCTAATTAA[C/T]GTATGCATTGCATCA | 7525 |
rs577086159 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:745617 | ATGTGTAAATAAGTG[C/T]GTTAAATCTTAAGAG | 7525 |
rs577136951 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:740803 | TTACCATGTTCTCCC[A/G]ATTAAATAATTCTTA | 7525 |
rs577225305 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:737183 | ACTGGCTGGGTGCGG[G/T]GGCCCACACCTATAA | 7525 |
rs577237096 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:782277 | ATAGTCCCAGAGTTA[C/G]TATTTTCATTTTAGA | 7525 |
rs577238202 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:790843 | CAGGATGCTTTCTTG[G/T]TTGTAGTATCCTTCC | 7525 |
rs577240965 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:725099 | ATTACTTCTGTGAAA[C/G]TTTCCTTATCTAATA | 7525 |
rs577251381 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:746561 | GAAAATGAGAAGAAA[A/G]ACAAAAGGACAAAAC | 7525 |
rs577294607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:740082 | TCGCTTTGATCAATA[C/T]CCCAATTCTGATTCA | 7525 |
rs577323333 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:749355 | ATACAAAAATTAGGT[A/G]GGAGTGGTGGCGTGT | 7525 |
rs577364583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:810113 | ACTATAATGCTAATA[A/G]AATAAACGATGTCTA | 7525 |
rs577369114 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:755810 | CCTGAAACTCACTCT[A/G]CCTTTTTAAGCCAGC | 7525 |
rs577387204 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:731566 | CTTTCACTCTCAACA[A/T]TAGGATACTTCAGTA | 7525 |
rs577391745 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:788806 | TGGTGTGCGCCTGTA[C/G]TGCCAGCTAGTTGGG | 7525 |
rs577399525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:753750 | GTCGGCCTCCCAAAG[C/T]GCTAGAATTAAAGGT | 7525 |
rs577420987 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:797770 | CACCTTTTAAGACAT[-/C]ATCTAATCATTCTTC | 7525 |
rs577430484 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:781590 | GACAAGAAAAATTTC[C/T]CTCTTGTAGCTTAGC | 7525 |
rs577523778 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | YES1 | GRCh38.p7 | 18:743906 | GTGAGATTCTGACTC[A/G]AAAAAAAAAAAAATA | 7525 |
rs577573330 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776318 | CGTGCCTCAGCCTCC[C/T]ATGTAGCTGGGATTA | 7525 |
rs577631795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:770602 | TATCTCTTCATCTTG[C/T]TCTTTGCTCAAGATT | 7525 |
rs577649768 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:749365 | TAGGTGGGAGTGGTG[G/T]CGTGTGCCTGTAATC | 7525 |
rs577712424 | snp | A/G | 1.72895e-05 | 0.00294015 | intron-variant | YES1 | GRCh38.p7 | 18:743443 | ATAAACTATACTGTA[A/G]TATCAATTACAAAAA | 7525 |
rs577718482 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812816 | AGTTTTTTTGGTTGG[C/G]TGTTTGCTTCTCAGC | 7525 |
rs577758809 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:779177 | GAGGCTGAGGTGGGA[C/G]AATCACTTGAGTCCA | 7525 |
rs577796234 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:756469 | TCCTCAAGTAAGATA[A/T]CTTTCTTAAAGGCAG | 7525 |
rs577798707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:766742 | GTGACTGTTCAAATC[A/G]GTTTTTAAACTAAAG | 7525 |
rs577799592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:780828 | CTTTAACTGACTTCC[A/G]TCCTTCTACAGTGTT | 7525 |
rs577860695 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:773654 | CATAATCCTGTCCAT[C/T]GTATAATAACTTTCC | 7525 |
rs577893431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:766178 | GCCTATCCAGCCCTA[C/T]GTAGTAAATATTGAT | 7525 |
rs577900293 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:751466 | CCTCAGTAACTCTTC[A/C]TTCTTAAATCTCTAC | 7525 |
rs577909794 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812396 | TACCTGCGCGCGCCG[C/T]CGTCCGCTCACCGGA | 7525 |
rs577962672 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:795122 | AGGTACTGAGGGTTA[C/G]GACCCTTTTGGGGAA | 7525 |
rs577963487 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:794571 | GCTGTAGAAAAAAAA[C/T]GGCTTAAAATAACAA | 7525 |
rs577967374 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722815 | AAGTGAATGTAGGCT[A/G]GGCGCGGTGGCTCAC | 7525 |
rs578003656 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722324 | AAAAAACAACCACAA[G/T]TTTTAGTACCAGAAC | 7525 |
rs578030196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:761814 | TTGAAATATTACTAA[C/T]GTCATACGTGATTCA | 7525 |
rs578055149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:762276 | GGTGAGCCGAGATTG[C/T]GTCATTGCACTCCAG | 7525 |
rs578064909 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:801132 | GCCTGGGCAACAGAG[A/C]GAGACTCCATCTCAA | 7525 |
rs578078741 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:794366 | AATATCAATGTCATG[A/G]AAGATAAAGCCTGAA | 7525 |
rs578086788 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:738668 | GCATTCCAGCCTGGG[C/T]GACAGAGCGAGACTC | 7525 |
rs578091859 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:745639 | TCTTAAGAGAAATGA[C/G]GATATGGATTTTGTC | 7525 |
rs578115175 | in-del | -/GGCTACA | 0.00717158 | 0.0594505 | intron-variant | YES1 | GRCh38.p7 | 18:749137 | CTGGACTCCAGCCTG[-/GGCTACA]GAGCGAGACTCCATC | 7525 |
rs578164099 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:807482 | CCAGTCTGGGCAACA[C/G]AGCAAGATCCTGTCT | 7525 |
rs578165675 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:800788 | GGTGGTGGCTCATGC[C/T]TATAATCTCAGCACT | 7525 |
rs745332365 | snp | C/T | 1.97027e-05 | 0.00313862 | intron-variant | YES1 | GRCh38.p7 | 18:739836 | ACAGCAAGATATTCA[C/T]AAAAAATAAGCAAAT | 7525 |
rs745358195 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:726230 | AGAGATTGAGACCAT[A/C]CTGGCCAACATGGTG | 7525 |
rs745371231 | snp | C/G | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:814030 | TAAGGTGGCTTTGAA[C/G]ATGTTCTATATGGAG | 7525 |
rs745416021 | snp | C/T | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776071 | GATGTAACCTTGCAA[C/T]AGATTGCTGGGTCAA | 7525 |
rs745418909 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:726148 | CTTCACTCAAAGGCC[A/G]GGTGCGGTGGCTCAT | 7525 |
rs745465383 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:755120 | AAAGACTTAGAAATG[C/T]CCTCATGGCCATCTA | 7525 |
rs745546227 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:747695 | CATAAAAGAGAGAGA[A/C]TAGGCATAAGGAAAT | 7525 |
rs745577797 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:801863 | AAAGAAACTTGATTG[A/G]GAAAACATGCTCTGT | 7525 |
rs745604838 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:788724 | CAGGAGTTTGAGACC[A/G]GCCTGGCCAATTTGG | 7525 |
rs745627222 | in-del | -/AAAAA | | | intron-variant | YES1 | GRCh38.p7 | 18:742460 | CCCCAGTCTCTATTT[-/AAAAA]AAAAAAAAAAAAGAA | 7525 |
rs745629985 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:797026 | TAACATCATCTTCAA[C/G]TGGAGAAAATATTCT | 7525 |
rs745654368 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:771862 | AAAGTATTTCCTTAT[A/G]TATCTGCTTGGTAAG | 7525 |
rs745674133 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:801464 | GTACCAAGATGTATG[C/T]AGGAAACTGCTATTC | 7525 |
rs745748861 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:763455 | ATCTCAGCATTTTGG[A/G]AAGCTGAGGTGGAAA | 7525 |
rs745757580 | snp | G/T | 1.69654e-05 | 0.00291246 | missense | YES1 | GRCh38.p7 | 18:739736 | ATATATACAGATACC[G/T]GAGCAGCCATATCAA | 7525 |
rs745764663 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:727898 | TGACTGTTGTTCCTG[C/T]GTAGATAATATATAG | 7525 |
rs745882647 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:808154 | GCAGACCAGGATATA[C/T]TGCCATCAAGTCTGC | 7525 |
rs745920676 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:792893 | AAATCAACACCCACC[C/T]CTACTTTTTAATAAC | 7525 |
rs745928234 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:760401 | CTTGAATCTGGGAGG[C/T]GGAGGTTGCAGTAAG | 7525 |
rs745941501 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:807331 | GAGTGATACTTCATC[-/A]AAAAAAAAAAAAAAA | 7525 |
rs745956050 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:781977 | TGGAATTCAGGGTCA[C/T]AAGAGAAACTAGAAC | 7525 |
rs745992838 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | YES1 | GRCh38.p7 | 18:756751 | TGGCTCACACTTGTA[C/T]TGACAGGCTCTGGAG | 7525 |
rs746020174 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:759328 | AAAAATTAGCTGGGC[A/G]AGGTGGCGGGCGCCT | 7525 |
rs746020360 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:773030 | GCTGTGGACTAGAAG[A/G]TACTATGATGACTGG | 7525 |
rs746065182 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon | YES1 | GRCh38.p7 | 18:724546 | AACACAGATTCATCA[A/G]TTCATGGAGGGATTC | 7525 |
rs746080500 | snp | A/G | 1.65091e-05 | 0.00287303 | missense | YES1 | GRCh38.p7 | 18:745737 | ACCAATTTCTGCAGA[A/G]TATCAAATTGTGCTC | 7525 |
rs746141725 | snp | C/T | 1.64898e-05 | 0.00287135 | missense | YES1 | GRCh38.p7 | 18:743383 | CAGTTGGACACACAG[C/T]TGTCAACTTGTGGCA | 7525 |
rs746152853 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:804439 | ATGGTGAAACCCCCA[A/T]CTCTACTAAAAATAA | 7525 |
rs746168302 | snp | C/T | 5.1729e-05 | 0.00508545 | intron-variant | YES1 | GRCh38.p7 | 18:736769 | GAGTTAAGCAAAACA[C/T]ACAACACATTACAAG | 7525 |
rs746184572 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:811614 | ATGTTGCGGTTTTCA[A/G]TCAAACCAAGTAAAG | 7525 |
rs746186632 | snp | C/T | 8.23798e-05 | 0.00641741 | intron-variant | YES1 | GRCh38.p7 | 18:748037 | CAACACATAAAACAG[C/T]AATCACCGCAAGGTA | 7525 |
rs746194506 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:768272 | AAATTTTAAAATCTC[C/T]ACAAATTTTAATCAT | 7525 |
rs746215771 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:738794 | AAATTATCTGTTGAA[A/C]TATAAATACATATAG | 7525 |
rs746260786 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:800911 | CCAGCACTTTGGGAG[A/G]CCAAGGCGGGTGGAT | 7525 |
rs746275160 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:769234 | CATATTCCTGTCTTT[A/C]AAGTGACGTGCGACC | 7525 |
rs746306731 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:744394 | TTAGGAGATTTTTTC[-/T]TTTTTTTTTTTTTGA | 7525 |
rs746370293 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:732141 | AAGGCAAGTACATAT[C/T]TAAAAAAATATACCA | 7525 |
rs746389614 | snp | A/G | 1.69818e-05 | 0.00291387 | missense | YES1 | GRCh38.p7 | 18:736943 | TCATTCTTTCAATAT[A/G]TGCCATACCATCAGC | 7525 |
rs746412325 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:763762 | GCCAGTGATAATGGG[A/G]GAAATGAGAAGTGTA | 7525 |
rs746427225 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:781034 | AGCACTTTGGGGCCC[A/G]AGGTGGGTGGATCAC | 7525 |
rs746473585 | snp | G/T | 1.65356e-05 | 0.00287533 | missense | YES1 | GRCh38.p7 | 18:751777 | CTAGCTTCATAATCA[G/T]ATAAGGCCACAAATA | 7525 |
rs746474568 | snp | A/C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:777633 | CCAACATGCTGAAAC[A/C/G]CTGTTTCTACTAAAA | 7525 |
rs746504153 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:763821 | AATATGGAAAGAGGA[A/G]ACATTAAGAAAAAGT | 7525 |
rs746539304 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:809135 | TAAACATTTTGATTA[C/T]CTTCTATTGGTTATT | 7525 |
rs746555356 | in-del | -/TCTCT | | | intron-variant | YES1 | GRCh38.p7 | 18:792550 | CTCTCTCTCTCTCTC[-/TCTCT]CCCTCTGTATATGTG | 7525 |
rs746573126 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:729184 | TTAATGTGTCTGAAT[A/C]CACTAATCTTGTCTT | 7525 |
rs746617543 | snp | C/T | 1.87345e-05 | 0.00306054 | intron-variant | YES1 | GRCh38.p7 | 18:739822 | GCTTCCTGTAACAGA[C/T]AGCAAGATATTCATA | 7525 |
rs746626928 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:741073 | CAGCTGTTTTTTGTA[C/T]TTTTAGCAGAGACGG | 7525 |
rs746722267 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:790905 | TTCCCAACTGTTACC[A/G]AGGTTTCTCAGAAAT | 7525 |
rs746748992 | snp | C/T | 3.295e-05 | 0.00405881 | synonymous-codon | YES1 | GRCh38.p7 | 18:743342 | TTCCCAAGCATCTTT[C/T]GCTAGACCTTGAGTC | 7525 |
rs746750223 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:748532 | TGTACCCATTAGCAG[G/T]CACTCTGCACCCCCA | 7525 |
rs746760274 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:738797 | TATCTGTTGAAATAT[-/A]AAATACATATAGACT | 7525 |
rs746767586 | snp | A/G | 3.69959e-05 | 0.00430077 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724383 | CTACACAAGTTCTTT[A/G]TATTTTGGCAGATTT | 7525 |
rs746784197 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:779209 | CAGTTCAGGACCAGC[C/T]TGGGCAACAAAAGGA | 7525 |
rs746784334 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:785725 | TGGGTTTGTTATAAA[A/G]GCCAGTCTGTCAAGA | 7525 |
rs746805246 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:751118 | GGAACATGGATGGAA[A/G]AAAATACGACTGGAA | 7525 |
rs746858112 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:735411 | TGGAAAACCAAATAT[C/T]GTATGGTCTCACTTA | 7525 |
rs746878404 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:751390 | TGGTACTTAGAAAAA[C/T]AGGAGCATCAAACTC | 7525 |
rs746922028 | snp | C/G | 1.64789e-05 | 0.0028704 | missense | YES1 | GRCh38.p7 | 18:724489 | CTTCCAAGAAGGACT[C/G]AATATATTCAAATGT | 7525 |
rs746940608 | snp | C/G | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775949 | TTTTATATGAATATA[C/G]CATAGGTAAGGGATA | 7525 |
rs747014698 | snp | C/G | 9.88338e-05 | 0.00702902 | missense | YES1 | GRCh38.p7 | 18:756655 | CCAAATGGTGTCATG[C/G]AAAGACTGCTGAAAT | 7525 |
rs747077803 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:746330 | TAGAGAGGGAAAGGC[A/C]GCAAAATAACAGACC | 7525 |
rs747113229 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:783095 | ATATTTTTAAAAATT[A/C]TATAGCCACTAGGTT | 7525 |
rs747158831 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:732255 | ACCAGCTTAGCCAAC[A/G]TGGCAAAACCCCATC | 7525 |
rs747165691 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:782407 | AGAGGCAGGGTCACT[A/G]ATGGAACATGGCAGA | 7525 |
rs747200359 | snp | C/T | 1.65097e-05 | 0.00287308 | missense | YES1 | GRCh38.p7 | 18:743263 | CAGGCTTCTTACCCA[C/T]CCACACTTCGCCGAA | 7525 |
rs747218451 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:755611 | TGTATAGTCAGTCTA[C/T]GCTTGTAGTGGGGAT | 7525 |
rs747227284 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:757502 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 7525 |
rs747250955 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:794601 | AATTTATTATGTCAT[A/G]GTTCTGGAGGCAGGA | 7525 |
rs747275534 | snp | A/C | 1.84449e-05 | 0.00303679 | intron-variant | YES1 | GRCh38.p7 | 18:745943 | TAATATAACAATATT[A/C]ATACCTTTAGTTGTT | 7525 |
rs747324459 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:807097 | CAACACGGTGAGACC[C/T]CATCTCTCCAAAAAA | 7525 |
rs747335282 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:801991 | CAGCATTTGCTACAG[C/T]TGTTAGTGTAATAAC | 7525 |
rs747350395 | in-del | -/AAAC | | | intron-variant | YES1 | GRCh38.p7 | 18:743505 | GTTTAAACTGTAGAA[-/AAAC]AAAAACAGAAGTCCT | 7525 |
rs747431184 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:733430 | TGTTAATTAACTCAA[A/G]TACTTACTGTATATC | 7525 |
rs747436806 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:756181 | ATTAAGTAACCACTA[C/T]AAGACTTTAATACTG | 7525 |
rs747446238 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:769310 | TGACTGTACTAAACT[C/G]TTATGATTTCTAGTA | 7525 |
rs747522313 | in-del | -/CAAA | 3.33622e-05 | 0.00408412 | intron-variant | YES1 | GRCh38.p7 | 18:756522 | CCAAGGTGATGTTCT[-/CAAA]CAGACAACATAATTG | 7525 |
rs747544867 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:768518 | TATCTCTAGACACTA[C/T]GGTTTATGCCATTAT | 7525 |
rs747552847 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:764614 | GTTTCAGATGGTTCG[-/T]TTTAGGTTCATGCTG | 7525 |
rs747579580 | snp | A/T | 1.64732e-05 | 0.0028699 | synonymous-codon, intron-variant | YES1 | GRCh38.p7 | 18:732916 | CTTTATTGTAAACCG[A/T]CCATACAGTGCAGCT | 7525 |
rs747602616 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:767061 | CATGTTCATCTGTAA[C/G]TCTGAACTCTTCTGT | 7525 |
rs747616089 | snp | A/C | 1.65597e-05 | 0.00287743 | intron-variant | YES1 | GRCh38.p7 | 18:746089 | GAATTGAAAAGTATG[A/C]GGTTCAGAAAAATTA | 7525 |
rs747625158 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:785925 | CCTGGGCAAAAGAGT[C/G]ACACTGTCTTTTTAA | 7525 |
rs747647794 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:751294 | ACTTAATTTCATCAA[C/T]TGGAAAGTAGATGGG | 7525 |
rs747669580 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:799949 | CTGGACATATATTTA[C/T]GGAATATGATATAAA | 7525 |
rs747712152 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:743979 | TACTAATATATAGTA[A/G]ATATATTGTATTTAC | 7525 |
rs747726944 | snp | A/C/G | 0.000115588 | 0.00760143 | missense | YES1 | GRCh38.p7 | 18:751748 | CCTTCTTAAATGAAA[A/C/G]GTCTTCTGTAGTTCT | 7525 |
rs747772462 | snp | A/G | 1.69911e-05 | 0.00291466 | missense | YES1 | GRCh38.p7 | 18:736945 | ATTCTTTCAATATAT[A/G]CCATACCATCAGCAA | 7525 |
rs747796962 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:807648 | AGCTGATAACGTATT[G/T]GCAACTGTTGATGTC | 7525 |
rs747838528 | in-del | -/GA | 1.99148e-05 | 0.00315547 | intron-variant | YES1 | GRCh38.p7 | 18:736997 | AAACACAAGACATAC[-/GA]TACAAAGGGAAGCAG | 7525 |
rs747840679 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:809269 | TTAGAAATTTTTTCC[C/G]AAAAATTCTCTAATT | 7525 |
rs747858795 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:766377 | GCTCCACATCCTTAA[C/G]ACTTGTTATTAACAC | 7525 |
rs747870034 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:729344 | CGCTGGAACCTGGGA[A/G]GCGGAGGCTGCAGTG | 7525 |
rs747890953 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | YES1 | GRCh38.p7 | 18:756719 | ATGGTGACACTGTAG[C/T]GGGTTCTGCTCCATA | 7525 |
rs747911072 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:806129 | TTTTGTCCTAGGTAT[A/T]TATGAACAAGTCATA | 7525 |
rs747922199 | snp | C/T | 1.65315e-05 | 0.00287498 | missense | YES1 | GRCh38.p7 | 18:743017 | TTTTCATTATCTGAG[C/T]TTCTTGAAGGAAAGC | 7525 |
rs747979757 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:770073 | CAAGGGATTCTCCTG[C/T]CTCAGCCTCCCAAGT | 7525 |
rs747985513 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | YES1 | GRCh38.p7 | 18:756640 | ACCCCTGAGGATCCT[C/T]CAAATGGTGTCATGG | 7525 |
rs748017548 | snp | A/C | 9.28514e-05 | 0.00681301 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724375 | TAGAAAATCTACACA[A/C]GTTCTTTATATTTTG | 7525 |
rs748052452 | in-del | -/G | | | intron-variant | YES1 | GRCh38.p7 | 18:737640 | TAACCACAAGGTATA[-/G]GTTCCCAAACTACAG | 7525 |
rs748072109 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:752700 | GTAATCTCAGCACTT[C/T]GGGAGGCCGAGGTGG | 7525 |
rs748180592 | snp | C/T | 0.000444675 | 0.0149044 | synonymous-codon, intron-variant | YES1 | GRCh38.p7 | 18:732871 | TGTTACTAGTTCTGT[C/T]TGCAGAATTCCAAAT | 7525 |
rs748182450 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:786937 | GTATTCCCTCTAGGA[C/G]GAATGGTTCAGTCTT | 7525 |
rs748267139 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:747626 | GGCAAATTTTTGAAG[G/T]GAGACAGTCTGAAAA | 7525 |
rs748318798 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:786408 | AGAGCTAAGGAAACC[C/T]AAAATAGAATCTTTG | 7525 |
rs748370938 | snp | A/G | 1.65433e-05 | 0.002876 | intron-variant | YES1 | GRCh38.p7 | 18:733011 | GTTTTTTAAAAATCT[A/G]TTTGTGTAAACATAG | 7525 |
rs748385866 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:733611 | ACATGGTGAAACCCC[A/G]TCTCTACCAAAAATA | 7525 |
rs748387629 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:783200 | TCTGCCTGGGCAAAA[C/T]AGCTAGACCCCATCT | 7525 |
rs748458497 | snp | A/G | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723021 | GGTGTGAACCTGGGA[A/G]GCAGAGCTTGCAGTG | 7525 |
rs748509962 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:758836 | TTACCTACCGTATTA[C/T]CTATCATATAGGTTT | 7525 |
rs748514959 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:784649 | TAGCTTGTGGGGGCT[G/T]CCCACATTCCTTGGC | 7525 |
rs748543357 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:777694 | CGCCTGTAATCCCAG[C/G]TACTTGGGAGGCTGA | 7525 |
rs748559394 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:808016 | GGGGGAAAAGGAGTT[G/T]AGGCACAGAGGCTTG | 7525 |
rs748599712 | snp | A/G | | | missense | YES1 | GRCh38.p7 | 18:756649 | GATCCTCCAAATGGT[A/G]TCATGGAAAGACTGC | 7525 |
rs748626402 | snp | A/G | 3.34024e-05 | 0.00408657 | intron-variant | YES1 | GRCh38.p7 | 18:724666 | ACATTAAAGAACAAT[A/G]GTCCTAACTACCACT | 7525 |
rs748628113 | snp | A/G | 1.86745e-05 | 0.00305563 | intron-variant | YES1 | GRCh38.p7 | 18:745932 | TATACTTATACTAAT[A/G]TAACAATATTCATAC | 7525 |
rs748661316 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:803455 | TACAAACTCCATATT[A/G]TAACACTCCTCATTT | 7525 |
rs748672426 | in-del | -/TGAATTAAAGGAAG | | | intron-variant | YES1 | GRCh38.p7 | 18:748191 | AAAAAATAGGTTACA[-/TGAATTAAAGGAAG]CACAATTGCATACTT | 7525 |
rs748689240 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:746109 | CAGAAAAATTATACA[C/G]AAGTGTCAGTAAGAA | 7525 |
rs748715989 | snp | C/T | 0.000115467 | 0.00759737 | synonymous-codon | YES1 | GRCh38.p7 | 18:745802 | CCTAATTTTGTAGTG[C/T]TTCACATTGTCACCC | 7525 |
rs748718591 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:800873 | AAAACAAAGGCTGGG[C/T]GTGGTGGCTCACGAC | 7525 |
rs748736105 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:810402 | AATATTATACTTCGA[C/T]CACAAGACAAATTCC | 7525 |
rs748767422 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:787435 | ATTTGTTGGGCTGGG[C/T]GCGGTGGCTCACACC | 7525 |
rs748787911 | in-del | -/ATATTTTAAA | 1.76064e-05 | 0.00296697 | intron-variant | YES1 | GRCh38.p7 | 18:743126 | ACATTTTAGGAATTT[-/ATATTTTAAA]GGATTTTAGACCAAA | 7525 |
rs748796323 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:737251 | TGAGGTCATGAGTTC[A/G]AGATCAGCCTGGCCA | 7525 |
rs748804933 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:752859 | GAGACAGGAGAATCG[C/T]TTGAAACCCGGAAGT | 7525 |
rs748818575 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:788456 | ATAACGATGTGTATA[C/T]ATTTAAAATTTTGTT | 7525 |
rs748842735 | in-del | -/TAACT | 1.67473e-05 | 0.00289368 | intron-variant | YES1 | GRCh38.p7 | 18:751843 | GGTAAATTATGTAGC[-/TAACT]TAACAAAACAGAAAA | 7525 |
rs748885017 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:769171 | TATGTAAGCACACTG[A/C]ATGATGTTCACACAA | 7525 |
rs748889148 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:751501 | TATGGCAGAACCACA[A/G]CAGCACAAATTGTAG | 7525 |
rs748892826 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:768092 | TTTGTGGACCATATG[G/T]TGTCTGTAACAACTA | 7525 |
rs749028233 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:800108 | AAATTCATCCTGAGC[A/G]TTAATGATACTAGTT | 7525 |
rs749053147 | snp | C/T | 1.64798e-05 | 0.00287047 | missense | YES1 | GRCh38.p7 | 18:756566 | TCTCACCTGTTAAAC[C/T]AGCAGGATATGAACT | 7525 |
rs749063474 | in-del | -/AC | | | intron-variant | YES1 | GRCh38.p7 | 18:733282 | GTGTAACTTTTAAGT[-/AC]AGTCTGGCACCTAAT | 7525 |
rs749090036 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:796489 | GAAACAAACAATTAG[A/G]CCGGGTGCAGTGGCT | 7525 |
rs749098848 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:762629 | TAACATACATTATGG[G/T]ATTAAAAAAAACTAT | 7525 |
rs749138916 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:724787 | TTAAACATGAGAATA[C/T]CAAGAAGAGCTTAGA | 7525 |
rs749160772 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:774724 | TAATAGCCTAACTGG[C/T]CTCCCAGTTCCTGCC | 7525 |
rs749256631 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:757296 | ATCACGAGGTCAGGA[A/G]ATTGAGACCATCCTG | 7525 |
rs749259911 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:725893 | CATCTCGCGGGGTGG[C/G]GAAGTGAAATCCAGT | 7525 |
rs749289407 | snp | A/G | 2.24631e-05 | 0.00335127 | intron-variant | YES1 | GRCh38.p7 | 18:739857 | ATAAGCAAATCTTAT[A/G]TTAGGATTGAAATGA | 7525 |
rs749362388 | snp | G/T | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776327 | GCCTCCCATGTAGCT[G/T]GGATTACAGGCTCAT | 7525 |
rs749375553 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:771998 | AAAATCAGAAATTAC[A/C]AGACAGTCTGATCGT | 7525 |
rs749424791 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:734606 | TACAACATACAACAT[C/G]ACTAATCATCAGGGA | 7525 |
rs749518116 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:771131 | CACTTTGGGAGGCCC[-/A]AGGCAGGCAGATCAC | 7525 |
rs749541286 | snp | A/T | 4.98219e-05 | 0.00499084 | intron-variant | YES1 | GRCh38.p7 | 18:724645 | TACCTAATACACAAG[A/T]TTAAAACATTAAAGA | 7525 |
rs749556561 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:738548 | ACAAAAGATTGGCTG[C/G]GGGTGGTGGTGGGCG | 7525 |
rs749594495 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:779620 | TTGTTGGCAGAAAGG[C/G]ACCTATCAAGTACTA | 7525 |
rs749667147 | in-del | -/AAAA | | | intron-variant | YES1 | GRCh38.p7 | 18:742461 | CCCAGTCTCTATTTA[-/AAAA]AAAAAAAAAAAAGAA | 7525 |
rs749697441 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:780810 | GGATTATTGCAAAAG[A/C]CTCTTTAACTGACTT | 7525 |
rs749728499 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:812013 | CCCGCGGGGGCGGGG[A/G]ACCGCGGCGGCGGCG | 7525 |
rs749798069 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:729500 | GCTCAAATTCTCCAG[C/T]TTTTCATTATTTTGC | 7525 |
rs749885349 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | YES1 | GRCh38.p7 | 18:756622 | GCACCTCCAAAAGGC[A/G]TTACCCCTGAGGATC | 7525 |
rs749887231 | in-del | -/CCC | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812329 | CTCCACCTCCTCCGC[-/CCC]CCCCCCCCGGCCCCG | 7525 |
rs749894325 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:756038 | AAATCTGAGCTCTCC[C/T]ACTTACTATCTGTGA | 7525 |
rs749923760 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:780540 | TCATATGCCACCCCA[C/T]GACCTTGGACTTCTC | 7525 |
rs749931620 | in-del | -/TTG | | | intron-variant | YES1 | GRCh38.p7 | 18:750984 | ATTCTCAATGAATGA[-/TTG]TTGTTATCATTGTCG | 7525 |
rs749943750 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:744689 | CCACCACGCCTGGCC[-/T]TTTTTTTTTTTTTTT | 7525 |
rs749995362 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:758441 | CAACTTTATTTCCTA[C/T]TGTCCTCATACTTAC | 7525 |
rs750010373 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:734283 | AACTTGGCCAGGCGC[A/G]GTGGCTCACGCCTGT | 7525 |
rs750062336 | snp | A/G | 1.77988e-05 | 0.00298313 | intron-variant | YES1 | GRCh38.p7 | 18:743136 | AATTTATATTTTAAA[A/G]GATTTTAGACCAAAC | 7525 |
rs750068733 | in-del | -/TATTA | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722042 | CTACTATACAATTGT[-/TATTA]TATAAGGAACTGCTC | 7525 |
rs750080195 | snp | C/T | 1.72662e-05 | 0.00293817 | missense | YES1 | GRCh38.p7 | 18:742944 | AATTCAGTGACAATG[C/T]AAATTGGTTCTTCAG | 7525 |
rs750093491 | in-del | -/ACC | | | intron-variant | YES1 | GRCh38.p7 | 18:812014 | CCGCGGGGGCGGGGA[-/ACC]GCGGCGGCGGCGGCG | 7525 |
rs750117897 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:806434 | TAAAGAATTAACTTC[A/G]AGCTATGAAAAAGTA | 7525 |
rs750136957 | snp | C/T | 1.75496e-05 | 0.00296217 | intron-variant | YES1 | GRCh38.p7 | 18:745885 | TAAATACTTTCACTA[C/T]ATCTTTCTCAAAATA | 7525 |
rs750159470 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:809022 | AGTCAAAACTTAGGA[C/T]CTTGATGCCGTAATT | 7525 |
rs750170606 | snp | A/T | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813750 | ATTAAAATAGAAAAT[A/T]CCTTGAGCTGTTGCC | 7525 |
rs750222637 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:739392 | TTTGAGCCAAGGACT[C/T]TGAGACTAGCCTAAG | 7525 |
rs750257270 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:791999 | CAATTTGGACTAGCC[A/C]CATTTCAAGTGCTCA | 7525 |
rs750257679 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:766363 | AGATCAAATGACTTG[C/T]TCCACATCCTTAAGA | 7525 |
rs750348437 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:742149 | ATGAAATCAAACACA[C/T]AAAAATCAGGCCTGT | 7525 |
rs750379285 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:761691 | AATGCCTCACACATC[A/T]ACGCACTTATCTTTC | 7525 |
rs750379503 | snp | A/C | 1.7263e-05 | 0.00293789 | missense | YES1 | GRCh38.p7 | 18:746004 | TGATTTCCAGGATTC[A/C]AAAGTAATCTTTCAG | 7525 |
rs750393181 | snp | A/G | 3.29457e-05 | 0.00405854 | synonymous-codon, intron-variant | YES1 | GRCh38.p7 | 18:732838 | TGCAAGCTTACCTGG[A/G]TATGGCACTCGGCCC | 7525 |
rs750403509 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:728965 | GAGGTTCACTTAATC[C/T]GTGGGCTAGTATTTT | 7525 |
rs750432856 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:761158 | TCAATATATATCCAC[-/A]AAATATGTAAAAACT | 7525 |
rs750466108 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:809669 | ATAAATCTAATCCTA[C/T]TTGCAAAGGATAGCC | 7525 |
rs750468448 | in-del | -/ATTATT | | | intron-variant | YES1 | GRCh38.p7 | 18:793027 | TTAAGGTTCATTATA[-/ATTATT]ATTATTATTGGTTTT | 7525 |
rs750474995 | in-del | -/AT | 1.64768e-05 | 0.00287021 | intron-variant | YES1 | GRCh38.p7 | 18:732799 | CTGATAAAGCCACTC[-/AT]GAGATAACCAAGAGC | 7525 |
rs750476648 | snp | C/T | 1.70965e-05 | 0.00292369 | missense | YES1 | GRCh38.p7 | 18:739784 | AAATACTTTCCATCT[C/T]CTTCCTTAAGGAAAT | 7525 |
rs750535040 | snp | A/G | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722886 | TCACAAGGTCAGGAG[A/G]TCGAGACTATCCTGG | 7525 |
rs750568895 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:761716 | TCTTTCCAATAACTC[C/T]AGGATAGCCCATTAA | 7525 |
rs750597845 | in-del | -/GTT | 3.45545e-05 | 0.00415645 | cds-indel | YES1 | GRCh38.p7 | 18:745987 | CTAAGAAAATACCTC[-/GTT]GATTTCCAGGATTCA | 7525 |
rs750607137 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:754157 | AATCCTTTACTTAAT[C/G]TCTTCAGCAGTTTCT | 7525 |
rs750644702 | in-del | -/C | | | intron-variant | YES1 | GRCh38.p7 | 18:736738 | TCTTATTCTGGAAAA[-/C]CCTGTATAGTCAAGA | 7525 |
rs750645464 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:771029 | AAAAAAATCTGAAAA[A/G]TTAAAACCTAGAAAA | 7525 |
rs750761587 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:782892 | TAGAGACAGGGTTTC[A/G]CCATATTAGCCACTC | 7525 |
rs750807618 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:748609 | GGATATGCCCACTGC[A/T]TGCACCTTATATAAA | 7525 |
rs750812978 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:783877 | GCTCAGCCTCCCAAA[G/T]TGCTGGGATTACAGG | 7525 |
rs750831029 | snp | A/G/T | 4.94314e-05 | 0.00497128 | missense | YES1 | GRCh38.p7 | 18:724581 | CAGCCCTGAGGGCAC[A/G/T]GCATCCTGTATCCTC | 7525 |
rs750875128 | snp | A/C | 1.74772e-05 | 0.00295606 | intron-variant | YES1 | GRCh38.p7 | 18:739695 | CCACATTTTAATTTA[A/C]ACTTTTAATTCAAAT | 7525 |
rs750915746 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:726590 | TTTGAGACCAGCCTG[C/G]CCAACATGGCGAAAC | 7525 |
rs750944866 | snp | A/G | 1.69335e-05 | 0.00290972 | intron-variant | YES1 | GRCh38.p7 | 18:751849 | TTATGTAGCTAACTT[A/G]ACAAAACAGAAAAAA | 7525 |
rs750948220 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:747297 | CAATAGGCGAAACCC[A/C]GTCTCTACTAAAAAT | 7525 |
rs750979165 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:730620 | GCTTAATAAGACTTA[G/T]GCTTTCTGTCTGGGT | 7525 |
rs750991971 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:795319 | AATGGTGGTGGTGGG[C/G]ACACGTATACACACA | 7525 |
rs751039554 | snp | C/T | 3.30415e-05 | 0.00406444 | synonymous-codon | YES1 | GRCh38.p7 | 18:751719 | CGTATTGTTAATTAT[C/T]TGAAATCTTTCACCC | 7525 |
rs751108175 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:779103 | ATGAGAAGAGCCTGA[C/T]GTAAAGAATATGTAA | 7525 |
rs751127277 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:758581 | ACCTCTCTACCTGCT[A/G]AAATCCTATCCTTTC | 7525 |
rs751136666 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:744511 | TCTCCTGCCTCAGCC[C/T]CCCAAGTAGCTGAGC | 7525 |
rs751145666 | snp | A/C | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722316 | GTAAACAGAAAAAAC[A/C]ACCACAATTTTTAGT | 7525 |
rs751172198 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:754522 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCGTC | 7525 |
rs751172245 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:742296 | ATCTTGTGGTCTAGA[C/G]TTAAGGAAAATGAAG | 7525 |
rs751198391 | snp | A/C | 4.94189e-05 | 0.00497062 | missense | YES1 | GRCh38.p7 | 18:756610 | AATGAGGAAGATGCA[A/C]CTCCAAAAGGCGTTA | 7525 |
rs751233510 | snp | C/T | 1.66882e-05 | 0.00288857 | intron-variant | YES1 | GRCh38.p7 | 18:756518 | TTACCCAAGGTGATG[C/T]TCTCAAACAGACAAC | 7525 |
rs751278344 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:799586 | AAGGTGGTGCATGCC[C/T]GTAATGAGCAACTCA | 7525 |
rs751304977 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:767740 | AGAGTCTCGCTCTGT[A/G]CCTAGGCTGGAGTAC | 7525 |
rs751334693 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:811050 | CGTAATTTAACTTTA[A/G]AAGTGTAACAGGATG | 7525 |
rs751354505 | in-del | -/AGG | | | intron-variant | YES1 | GRCh38.p7 | 18:742409 | GGACTGCCTGAGGCC[-/AGG]AGTTCAAGACCAGCC | 7525 |
rs751368444 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:781169 | AGCTACTCAGGAGGC[G/T]GAGGCAGAAGAATTG | 7525 |
rs751390392 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:800548 | CCCGCTAGAAAACAA[C/T]GTTCCAGCTTATTAG | 7525 |
rs751392942 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:780526 | CAAGAAAGCCCTTCT[C/T]ATATGCCACCCCATG | 7525 |
rs751400232 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:752266 | GCATGTGCCGCCACA[C/T]CTAGTTAATTTTTTT | 7525 |
rs751440542 | in-del | -/TTAA | 6.60273e-05 | 0.00574537 | intron-variant | YES1 | GRCh38.p7 | 18:732990 | TGTTGACCATCTTGC[-/TTAA]TTGTTTTTTAAAAAT | 7525 |
rs751453705 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:766720 | TTCCCATCTCTACTT[C/T]GGTGACGTGACTGTT | 7525 |
rs751526421 | snp | A/G | 1.72788e-05 | 0.00293923 | intron-variant | YES1 | GRCh38.p7 | 18:745881 | AAAATAAATACTTTC[A/G]CTATATCTTTCTCAA | 7525 |
rs751529841 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:724989 | ACTGAGGAATGGTGG[A/C]AAGATCCTGTCTGAA | 7525 |
rs751544565 | snp | A/C | 1.65726e-05 | 0.00287855 | missense | YES1 | GRCh38.p7 | 18:745724 | TGTGTAGTGTTTCAC[A/C]AATTTCTGCAGAGTA | 7525 |
rs751552293 | snp | A/C | 1.65556e-05 | 0.00287707 | missense | YES1 | GRCh38.p7 | 18:736904 | CAAGAATATTAGCAG[A/C]CCGAAGATCTCGGTG | 7525 |
rs751552816 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:740209 | GTAGCTAAATGAGTC[A/G]CTGTGGAACTACTGC | 7525 |
rs751567011 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:809852 | AATTACACTAAGACC[A/G]ATACCCTTGGTAACT | 7525 |
rs751577972 | in-del | -/AT | 1.66217e-05 | 0.0028828 | intron-variant | YES1 | GRCh38.p7 | 18:751687 | TATTTCTCTCACAAA[-/AT]ATATTCATGACACTT | 7525 |
rs751589789 | snp | G/T | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776998 | TATGAAAAACAAAAA[G/T]GCCAATTAGACATTA | 7525 |
rs751642626 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:764357 | CCTCCCAAGTAGCTG[C/G]GATTATAGGCATGTG | 7525 |
rs751691473 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:808606 | ATCTTACTAAAACTT[C/T]CTGTAAATATTCACA | 7525 |
rs751743445 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:788745 | GCCAATTTGGTGAAA[A/C]CCTGTCTCTACTAAA | 7525 |
rs751750413 | snp | C/T | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775734 | CCTGGGAGATAGAGG[C/T]TACAGTGAGCCGTGA | 7525 |
rs751762584 | in-del | -/CAGATAGGAAGGCATTC | | | intron-variant | YES1 | GRCh38.p7 | 18:736199 | CAACAACAAACATTA[-/CAGATAGGAAGGCATTC]CAGATAGGAAGGCAT | 7525 |
rs751882704 | snp | C/T | 6.59087e-05 | 0.00574021 | missense | YES1 | GRCh38.p7 | 18:743299 | CTTGTCCTAGTTTAA[C/T]CTCTAGTCGCAAAGA | 7525 |
rs751909567 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:785306 | AACCAAGTGATTGAG[A/T]CAATGGAGTTAACTC | 7525 |
rs751964488 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:771783 | ACAGGGATCCCCACA[A/C]TTCGGCCTTCCCTGG | 7525 |
rs751986438 | snp | C/T | 1.64743e-05 | 0.00287 | missense | YES1 | GRCh38.p7 | 18:748014 | CTTCCCACCAATCTC[C/T]TTCCCTGCAACACAT | 7525 |
rs752021580 | snp | C/T | 1.6775e-05 | 0.00289607 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724418 | ATATAAAATAGGCTA[C/T]TTGAATTATAAATTT | 7525 |
rs752033801 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:798203 | TCTTGTTTCAGAAAT[C/G]AGAAGATAAAAAGGA | 7525 |
rs752036417 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:798207 | GTTTCAGAAATGAGA[A/C]GATAAAAAGGAGATA | 7525 |
rs752044321 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:793750 | TAGTTTTGTAATATA[C/T]CAAAAATAGTTATAA | 7525 |
rs752105163 | snp | A/C | 1.69263e-05 | 0.0029091 | intron-variant | YES1 | GRCh38.p7 | 18:745702 | ACCTTTGAAATATTC[A/C]CATACCTGTGTAGTG | 7525 |
rs752208525 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:811157 | ATATCATGTGAAATC[C/G]ACTGTGAAAACACAC | 7525 |
rs752214006 | snp | A/G | 1.64901e-05 | 0.00287137 | missense | YES1 | GRCh38.p7 | 18:724452 | CCTGGCTGGTACTGT[A/G]GCTCTGTAGCAGTGA | 7525 |
rs752221232 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:798329 | CATCAATATTGTTTT[C/T]CCTTTTCTGAAACAT | 7525 |
rs752243502 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:780660 | GCCCTATATGGCCAA[C/T]TGGTCACCAGGACCT | 7525 |
rs752303389 | snp | G/T | 1.64781e-05 | 0.00287033 | synonymous-codon | YES1 | GRCh38.p7 | 18:724588 | GAGGGCACGGCATCC[G/T]GTATCCTCGCTCCAC | 7525 |
rs752305362 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:730816 | TGAAAGTTCCTCATG[A/G]TTATACATTTAAAGT | 7525 |
rs752306568 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:761327 | GCATCCAAAGTCTAA[A/T]TATCAAGAAAACAGC | 7525 |
rs752316286 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:731771 | AGGAGATCGAGACCA[G/T]CCTGGTTAACACGGT | 7525 |
rs752417947 | in-del | -/A | 1.65644e-05 | 0.00287783 | frameshift-variant | YES1 | GRCh38.p7 | 18:751791 | TATAAGGCCACAAAT[-/A]ATAGTAACACCACCT | 7525 |
rs752467869 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:801422 | TCACTTCCTCTAGAA[G/T]TATAGCCTTGAATGG | 7525 |
rs752478600 | in-del | -/TTAT | | | intron-variant | YES1 | GRCh38.p7 | 18:768696 | GTTTAGATATGTTAT[-/TTAT]TTATTTATTTATTTA | 7525 |
rs752491547 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:738077 | AACAAAAATGGATTG[A/C]CAACCTCCCCTACCA | 7525 |
rs752549574 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:757286 | AGGCGGGCGGATCAC[A/G]AGGTCAGGAGATTGA | 7525 |
rs752569860 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:789399 | TCAGCCTGGGCAACA[C/T]AGGGAGAATCCTGTC | 7525 |
rs752596423 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:755852 | ACTTCAGTGAAAAAG[C/T]ATCCTGATACGGGAC | 7525 |
rs752661671 | snp | C/T | 4.9423e-05 | 0.00497082 | missense | YES1 | GRCh38.p7 | 18:743319 | AGTCGCAAAGATTCT[C/T]GAGGGATTTCCCAAG | 7525 |
rs752695748 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:790896 | AAGAGCTCCTTCCCA[A/G]CTGTTACCGAGGTTT | 7525 |
rs752721319 | snp | C/T | 2.00934e-05 | 0.00316959 | splice-acceptor-variant | YES1 | GRCh38.p7 | 18:746053 | TGCCAAAATACCATC[C/T]GGAAAAAAATTAAGT | 7525 |
rs752733560 | in-del | -/TGTGGGAGGCTGC | | | intron-variant | YES1 | GRCh38.p7 | 18:750433 | TTGATCATTCTTTGT[-/TGTGGGAGGCTGC]TGTGTGCGTTTTAAG | 7525 |
rs752803964 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:798343 | TTCCTTTTCTGAAAC[A/G]TCGGTCATTGTAAAA | 7525 |
rs752858699 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:799316 | GCTGACCTGCTAGAA[A/C]CTATTTTTTCCAGCT | 7525 |
rs752863428 | in-del | -/CAAAACAAAAACAAAAACCCC | | | intron-variant | YES1 | GRCh38.p7 | 18:789582 | AGCAAGACTCTGTCT[-/CAAAACAAAAACAAAAACCCC]CAAAACAAAAAAACC | 7525 |
rs752868837 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:778651 | ATCTTTAGGAAATCC[C/T]AGAAAAATAAATTTA | 7525 |
rs752889577 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:764707 | GATTAAACAAAAATA[A/G]TTTCATAATTTATCT | 7525 |
rs752901062 | snp | C/T | 1.64999e-05 | 0.00287222 | missense | YES1 | GRCh38.p7 | 18:736882 | TTGCACACAAGATTT[C/T]CTCCTACAAGAATAT | 7525 |
rs752933660 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:728857 | TTAGGAATGCTCAAT[A/C]TGCACCACCTCCTTA | 7525 |
rs752935953 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:728209 | CACACACCTGTGGTC[A/T]CAGCTACTTGGGAGG | 7525 |
rs752968083 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:749331 | AATGAAACCCTGTCC[C/T]TACTAAAAATACAAA | 7525 |
rs752996411 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:811796 | CTCCTCCCCGTCGCC[A/G]GGCGGTCCACACGAC | 7525 |
rs752997996 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:789244 | TTAAAATATTCATGA[C/T]CCAATACACTTATGT | 7525 |
rs753033349 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:805215 | AGCTGACTACAACCT[C/T]GGGCCATATAGTATG | 7525 |
rs753062108 | snp | A/C | 1.64768e-05 | 0.00287021 | stop-gained | YES1 | GRCh38.p7 | 18:742918 | GATACTAATACATAC[A/C]TTTTGACATAAATTC | 7525 |
rs753101192 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:772852 | CATTTGTGGTCTGCT[A/C]CAGGTTCCCTCTATC | 7525 |
rs753156030 | snp | A/G | 1.75133e-05 | 0.00295911 | intron-variant | YES1 | GRCh38.p7 | 18:743119 | AAATAACACATTTTA[A/G]GAATTTATATTTTAA | 7525 |
rs753182067 | snp | C/T | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723353 | TCCATGACATCAACA[C/T]TAAACATTACCTTCC | 7525 |
rs753193237 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:786360 | GAAGGGGAGCTTCAC[A/C]TAAGAGTGTCAAGTT | 7525 |
rs753197372 | snp | C/T | | | missense | YES1 | GRCh38.p7 | 18:739779 | GCTTCAAATACTTTC[C/T]ATCTCCTTCCTTAAG | 7525 |
rs753222928 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:735252 | TGGAGCCAATCTAAA[C/T]GACCATTGACCAATG | 7525 |
rs753235749 | snp | C/G | 7.03185e-05 | 0.00592911 | utr-variant-5-prime | YES1 | GRCh38.p7 | 18:756831 | AATGCAGCCCATTAT[C/G]AAATCTACAGAGACA | 7525 |
rs753298023 | snp | C/T | 5.02037e-05 | 0.00500993 | intron-variant | YES1 | GRCh38.p7 | 18:743215 | ATTGTTGCACTTTAA[C/T]CCACAGCTAAACAAT | 7525 |
rs753376692 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:782689 | AGGATTATTTTTTCT[C/T]TCTAATTTTAACTTT | 7525 |
rs753395913 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:769085 | CATGTTTGTAGCCTA[C/G]GAGCCATAGGCTATA | 7525 |
rs753413613 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:801709 | TATAGAGAGTGTGTA[C/T]GTGTATATACAGAGA | 7525 |
rs753438637 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:770411 | ATGTCTGTCAGTTCA[A/C]ATCAATCTGGTTGCT | 7525 |
rs753451492 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:746890 | TCATACTCTCTCCCT[C/T]TCTACATATGTATGT | 7525 |
rs753480264 | snp | C/T | 1.65343e-05 | 0.00287521 | synonymous-codon | YES1 | GRCh38.p7 | 18:724436 | GAATTATAAATTTTC[C/T]CCTGGCTGGTACTGT | 7525 |
rs753494627 | snp | A/T | 1.64757e-05 | 0.00287012 | synonymous-codon | YES1 | GRCh38.p7 | 18:743306 | TAGTTTAACCTCTAG[A/T]CGCAAAGATTCTCGA | 7525 |
rs753540070 | in-del | -/CA | | | intron-variant | YES1 | GRCh38.p7 | 18:764119 | AGCGAGACTCCCTCT[-/CA]AAAAAAAAAAAAAAG | 7525 |
rs753540118 | snp | C/T | 3.30229e-05 | 0.0040633 | intron-variant | YES1 | GRCh38.p7 | 18:732994 | GACCATCTTGCTTAA[C/T]TGTTTTTTAAAAATC | 7525 |
rs753621715 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:790289 | GCTGAGGCAGGAGAA[C/T]TGCTTGAACCCGAGA | 7525 |
rs753636437 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:727645 | ATATGCTTCCTTGGT[C/T]TATTGTATGTTACTC | 7525 |
rs753644262 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:761286 | AAAATCTTAAAAGTC[A/G]GTACAAGGAATTTAC | 7525 |
rs753664381 | in-del | -/CATTA | | | intron-variant | YES1 | GRCh38.p7 | 18:784205 | AATAATTATTGTTTT[-/CATTA]CAAGTTTTCTATATG | 7525 |
rs753674041 | snp | C/T | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:777009 | AAAAGGCCAATTAGA[C/T]ATTAACCACAAAAAT | 7525 |
rs753725334 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:740921 | TTATTTATTTGAAAC[A/G]GAGTCTCACTCAGTC | 7525 |
rs753726530 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:741909 | TGCTTTGGGTCTTTA[A/G]GTGTGTTCTGGCTAT | 7525 |
rs753775836 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon | YES1 | GRCh38.p7 | 18:756708 | AGATGACGGACATGG[C/T]GACACTGTAGTGGGT | 7525 |
rs753829901 | snp | C/T | 1.65195e-05 | 0.00287393 | synonymous-codon | YES1 | GRCh38.p7 | 18:736833 | TGTGTATTCATTGTC[C/T]TCAATTAACCTTGCT | 7525 |
rs753848363 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:786075 | AGCCTCCAGAACTGT[A/G]AGAAGTAAATTTCTC | 7525 |
rs753880159 | in-del | -/AC | | | intron-variant | YES1 | GRCh38.p7 | 18:809774 | TTCCTTAAAAAAACA[-/AC]AACAAATTCATGTAA | 7525 |
rs753906166 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:772966 | ACTGCACTAACCTGC[G/T]GACCAGTTATGGTTT | 7525 |
rs753926445 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:736496 | CGGTACAGGGCAATA[A/T]CTCCTCTGACTGAGA | 7525 |
rs754039021 | snp | C/G | 1.7959e-05 | 0.00299652 | missense | YES1 | GRCh38.p7 | 18:746031 | TCAGCATCTTTTCTC[C/G]CCATTTTGCCAAAAT | 7525 |
rs754091147 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:728250 | AGGATCACCTGAGCC[A/C]AGGGAGGTAGAGGCT | 7525 |
rs754157767 | snp | A/C | 1.83832e-05 | 0.00303171 | intron-variant | YES1 | GRCh38.p7 | 18:745912 | AATACTGCCCCAAGA[A/C]ATTTTATACTTATAC | 7525 |
rs754159577 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:759074 | TAAAATGTAGCTACA[G/T]ATATTAAAATAGAAG | 7525 |
rs754184668 | snp | C/T | 3.34538e-05 | 0.00408971 | intron-variant | YES1 | GRCh38.p7 | 18:756508 | TAAGTATATATTACC[C/T]AAGGTGATGTTCTCA | 7525 |
rs754189220 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:795151 | AACATAACTGAATCC[A/G]CAACTGCAAATTAGG | 7525 |
rs754203224 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:762785 | AACTAAAAATATTGT[A/G]TATTAGACACTGTAA | 7525 |
rs754211040 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:794123 | ATATGTTCATTTTGT[A/G]GTGATGAAACCTGAC | 7525 |
rs754225410 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:761569 | TAACCATCTTAAAGT[C/T]CTCTTCCCTCAAAAG | 7525 |
rs754240186 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:760203 | GACTGGGCACAGTGG[C/T]TCACACCTGTCATCC | 7525 |
rs754270303 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:729906 | TTGGGATTACAGGCG[G/T]GAGCCACAGCGCCCA | 7525 |
rs754272874 | snp | C/T | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723616 | CTAAAGATCAAAACA[C/T]TTCCCCTTTGATTGG | 7525 |
rs754311349 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:774174 | TCTTGGTTTCCCCCC[A/G]TCTTACTGGCTGCTC | 7525 |
rs754393572 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:779187 | TGGGAGAATCACTTG[A/G]GTCCAGCAGTTCAGG | 7525 |
rs754394895 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:725586 | TCTAACTAGGTACTG[C/T]CATCTTCATAAGTGA | 7525 |
rs754403994 | snp | C/T | 1.82463e-05 | 0.0030204 | intron-variant | YES1 | GRCh38.p7 | 18:739815 | CTAATAAGCTTCCTG[C/T]AACAGACAGCAAGAT | 7525 |
rs754486744 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:729347 | TGGAACCTGGGAGGC[A/G]GAGGCTGCAGTGAAC | 7525 |
rs754509357 | snp | C/T | 8.23771e-05 | 0.0064173 | missense | YES1 | GRCh38.p7 | 18:743307 | AGTTTAACCTCTAGT[C/T]GCAAAGATTCTCGAG | 7525 |
rs754527349 | snp | A/C | 1.772e-05 | 0.00297652 | utr-variant-5-prime | YES1 | GRCh38.p7 | 18:756833 | TGCAGCCCATTATCA[A/C]ATCTACAGAGACAAT | 7525 |
rs754615156 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:754668 | AGTGAGCCAAGACTG[A/C]GCCACTGCACTCCAG | 7525 |
rs754663681 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:791065 | TACCAGCCTGGCCAA[C/G]ATGGTGAAACCCCAT | 7525 |
rs754671227 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:800594 | CATTCTTAGATACAA[C/T]TGGAGAAATAAAAGG | 7525 |
rs754677266 | snp | C/T | 1.65157e-05 | 0.0028736 | synonymous-codon | YES1 | GRCh38.p7 | 18:724439 | TTATAAATTTTCTCC[C/T]GGCTGGTACTGTGGC | 7525 |
rs754695227 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:759745 | TACTCTAAGGTTGTA[G/T]GGTACATGTGCACAA | 7525 |
rs754740115 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:786788 | TATCTCTACCATAAA[A/G]TCAAATATACCTGCA | 7525 |
rs754774858 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:752445 | ACTGTAGCAACATCT[C/T]AGGCTTGGAAATGCA | 7525 |
rs754780823 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | YES1 | GRCh38.p7 | 18:756631 | AAAGGCGTTACCCCT[A/G]AGGATCCTCCAAATG | 7525 |
rs754781149 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:781338 | CTTGGCTCTTGATTT[A/C]TTTTAGATCCTCAAA | 7525 |
rs754804088 | in-del | -/TCA | 1.6596e-05 | 0.00288058 | intron-variant | YES1 | GRCh38.p7 | 18:751692 | TCTCTCACAAAATAT[-/TCA]TGACACTTACGTATT | 7525 |
rs754827724 | snp | A/T | 1.65201e-05 | 0.00287398 | intron-variant | YES1 | GRCh38.p7 | 18:733003 | GCTTAATTGTTTTTT[A/T]AAAATCTATTTGTGT | 7525 |
rs754829021 | snp | G/T | 1.64727e-05 | 0.00286986 | synonymous-codon | YES1 | GRCh38.p7 | 18:756714 | CGGACATGGTGACAC[G/T]GTAGTGGGTTCTGCT | 7525 |
rs754841809 | in-del | -/AGATTTTCTCCTACAAGAATATTAGCAGCCCGAAGATC | 1.64947e-05 | 0.00287177 | frameshift-variant | YES1 | GRCh38.p7 | 18:736876 | GCTATTTTGCACACA[lengthTooLong]TCGGTGAATATAGTT | 7525 |
rs754881506 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:809868 | ATACCCTTGGTAACT[C/T]CTACCAGGTTAAAAG | 7525 |
rs754930330 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:740411 | TTCAGAAGTAACAAT[A/G]CTATGGAAGACAGAG | 7525 |
rs754933365 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:811056 | TTAACTTTAGAAGTG[C/T]AACAGGATGGTTTAA | 7525 |
rs754970374 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:751125 | GGATGGAAGAAAATA[C/T]GACTGGAAGCAGACC | 7525 |
rs754971910 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:799660 | GTGAGCTGAGATCGC[A/G]CCACTGCATTCCAGC | 7525 |
rs754974220 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:806700 | TACAGTGCAAGGAGA[G/T]GTGTGTTTTGACATA | 7525 |
rs755004473 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:767764 | GGAGTACAGGGGCAC[C/G]ATCTCGGTTCACTGC | 7525 |
rs755026996 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:796930 | GAAAAAAAAATTACC[C/T]CACAACATACATAAA | 7525 |
rs755039976 | snp | A/G | 1.87271e-05 | 0.00305994 | intron-variant | YES1 | GRCh38.p7 | 18:745926 | AAATTTTATACTTAT[A/G]CTAATATAACAATAT | 7525 |
rs755057731 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:764460 | CTCCTGACCTCAAGT[A/G]ATCCACCTGCCTTGG | 7525 |
rs755075405 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:747552 | CCCTATCAACACACC[C/G]TCATATATAAGCTGT | 7525 |
rs755128887 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:749104 | AGGTGGAGGTTGCAG[C/T]GAGCCGAGATCATGC | 7525 |
rs755156149 | snp | C/T | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722916 | GCTAACACGGTGAAA[C/T]TGCGTCTCTACTAAA | 7525 |
rs755185326 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:795682 | ACACCGTATGTTCTC[A/T]CTTATAAGTGGGAGA | 7525 |
rs755199762 | snp | C/T | 3.29457e-05 | 0.00405854 | synonymous-codon, intron-variant | YES1 | GRCh38.p7 | 18:732862 | TCGGCCCTTTGTTAC[C/T]AGTTCTGTTTGCAGA | 7525 |
rs755216100 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:763161 | GTGTGAGGGGCTGTT[C/T]GTGAGCTGGGTAGGA | 7525 |
rs755222562 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:807126 | AATTCAAAAATTAGC[C/T]AGGCATGCTCCAGTC | 7525 |
rs755236105 | snp | A/G | 1.86538e-05 | 0.00305394 | synonymous-codon | YES1 | GRCh38.p7 | 18:746042 | TCTCCCCATTTTGCC[A/G]AAATACCATCTGGAA | 7525 |
rs755273828 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:807835 | GTCCAAAGAACCTAT[A/G]TGCCAGCAATTCTAC | 7525 |
rs755297635 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:771787 | GGATCCCCACACTTC[A/G]GCCTTCCCTGGGATT | 7525 |
rs755316094 | snp | A/G | 1.67013e-05 | 0.0028897 | intron-variant | YES1 | GRCh38.p7 | 18:756511 | GTATATATTACCCAA[A/G]GTGATGTTCTCAAAC | 7525 |
rs755351845 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:783766 | ATTACAGGCGCTGCC[-/A]ACCATGCCCAGCTAA | 7525 |
rs755352673 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:758796 | ATACACTCCTTCAAA[A/C]CAAGAGTTGTGCTTT | 7525 |
rs755369334 | in-del | -/AG | | | intron-variant | YES1 | GRCh38.p7 | 18:788219 | GCTGTTATATTAAAA[-/AG]AGATACAAAGTTTTT | 7525 |
rs755392569 | snp | C/G | 1.84391e-05 | 0.00303632 | intron-variant | YES1 | GRCh38.p7 | 18:739818 | ATAAGCTTCCTGTAA[C/G]AGACAGCAAGATATT | 7525 |
rs755410940 | snp | G/T | 1.72531e-05 | 0.00293705 | intron-variant | YES1 | GRCh38.p7 | 18:739712 | CTTTTAATTCAAATG[G/T]ATACATGTATATATA | 7525 |
rs755428240 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:768819 | GAGATTCTCGTGCCT[C/T]AGCCTCCCGAGTAGC | 7525 |
rs755472431 | snp | G/T | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:814054 | TATGGAGTTTTAAAG[G/T]TGGGAGAGTATGTCA | 7525 |
rs755521077 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:811177 | TGAAAACACACACCC[A/G]TGGAACGTATATACA | 7525 |
rs755525650 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:770902 | TTTAATCCCAACACT[C/T]TGGAAGGCTGAGGTG | 7525 |
rs755587747 | snp | A/G | 3.64877e-05 | 0.00427113 | intron-variant | YES1 | GRCh38.p7 | 18:742903 | ACAAATACCTAAGGA[A/G]ATACTAATACATACC | 7525 |
rs755615555 | snp | A/C | 1.684e-05 | 0.00290167 | synonymous-codon | YES1 | GRCh38.p7 | 18:742961 | AATTGGTTCTTCAGA[A/C]ACAACAGCATATAGT | 7525 |
rs755634074 | snp | C/T | 1.64728e-05 | 0.00286987 | missense | YES1 | GRCh38.p7 | 18:756626 | CTCCAAAAGGCGTTA[C/T]CCCTGAGGATCCTCC | 7525 |
rs755649830 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:767947 | CTCAAGTGATCCAAC[C/T]GCCTCGGCCTCCCAA | 7525 |
rs755649905 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:782504 | CTTAGGGCTCACTAC[C/T]CCATCTACTCAGTAA | 7525 |
rs755695679 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:746152 | GGTTTGGACGACAAA[G/T]AATAGCTAGAGAACA | 7525 |
rs755699210 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:769064 | CTACAGCATTCAGTA[C/T]AGTGACATGTTTGTA | 7525 |
rs755724435 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:731123 | GTTATCTGGAAAGAT[A/G]GCAAGTGGTGGTCAG | 7525 |
rs755755277 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:733064 | TCAATATCTCTACTG[C/T]AGTCATCAGTGTCAA | 7525 |
rs755788076 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:793705 | CACAGATTTCTATAG[A/G]GCAGCTACAAAAATA | 7525 |
rs755805607 | snp | G/T | 1.78229e-05 | 0.00298515 | intron-variant | YES1 | GRCh38.p7 | 18:743141 | ATATTTTAAAGGATT[G/T]TAGACCAAACTTCAG | 7525 |
rs755855177 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:789428 | TCTCTACAGAAAATT[A/T]AAAAATTAGCCAAGT | 7525 |
rs755870071 | snp | C/G | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775739 | GAGATAGAGGCTACA[C/G]TGAGCCGTGATTGTG | 7525 |
rs755881303 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:780678 | GTCACCAGGACCTGA[A/C]CATACTGCCCTGTAA | 7525 |
rs755891347 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:774644 | GACAACTTCTCTCCA[C/T]CTCCCACTGCTACCC | 7525 |
rs755913328 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:738091 | GCCAACCTCCCCTAC[C/T]ATAGAGTGTCTAACT | 7525 |
rs755951749 | snp | G/T | 1.76796e-05 | 0.00297312 | intron-variant | YES1 | GRCh38.p7 | 18:745889 | TACTTTCACTATATC[G/T]TTCTCAAAATACTGC | 7525 |
rs755971181 | snp | C/T | 3.29457e-05 | 0.00405854 | missense, intron-variant | YES1 | GRCh38.p7 | 18:732848 | CCTGGATATGGCACT[C/T]GGCCCTTTGTTACTA | 7525 |
rs756033072 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:800719 | CATTGGTAGCTTCTG[A/C]TGAGACTCTTCTTCC | 7525 |
rs756070807 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:737116 | GAAGATAACAGGAAA[A/T]CCAGAAAACATAATA | 7525 |
rs756085546 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:801441 | AGCCTTGAATGGCTG[A/T]TGAGTCTGTACCAAG | 7525 |
rs756087164 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:788402 | TACTTCTGGCTACAC[G/T]ATTTCAACCCTAAAA | 7525 |
rs756111151 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:783986 | TGTTTTGAGGATAAT[C/T]AGAAAAATCCATTTC | 7525 |
rs756173412 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:785453 | AAAGCTGGGCTTGTT[C/G]TAAGTAGCTTGTTCT | 7525 |
rs756187784 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:750943 | TCTGGGTATTAGAGT[C/T]AGAAGAGGGGAGAAG | 7525 |
rs756223001 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:778167 | AGGTTATTACATGCC[C/T]TGCTCAAGGACAGGG | 7525 |
rs756224201 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:771929 | TTGGACTGAAGAAGG[A/G]ATTTTATTGTAAAGA | 7525 |
rs756238312 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:734559 | AGACTCCATCTCAAA[A/G]ACAAAACAAAACAAA | 7525 |
rs756242495 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:735256 | GCCAATCTAAATGAC[C/T]ATTGACCAATGAGTG | 7525 |
rs756286616 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:728245 | GTGGGAGGATCACCT[A/G]AGCCCAGGGAGGTAG | 7525 |
rs756288996 | snp | C/T | 1.71111e-05 | 0.00292494 | missense | YES1 | GRCh38.p7 | 18:739785 | AATACTTTCCATCTC[C/T]TTCCTTAAGGAAATC | 7525 |
rs756329871 | in-del | -/AGG | | | intron-variant | YES1 | GRCh38.p7 | 18:737525 | CTTGTGTCTGTGGTT[-/AGG]AGAAGAGGTAAATCA | 7525 |
rs756376118 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:792485 | CATAGTCACACCTGT[A/G]AATAGCACTATACTC | 7525 |
rs756393484 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:796997 | ACAAAACAAAAACCT[A/G]TAAGTAGAATTTTTA | 7525 |
rs756432864 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:805216 | GCTGACTACAACCTT[A/G]GGCCATATAGTATGG | 7525 |
rs756440012 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:760110 | AATCCAGTCTATCAC[C/T]GAGGGACATCTGGGT | 7525 |
rs756442531 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:763336 | TGAATTATACAGCCT[A/G]GAAAGAAGAAAAAAT | 7525 |
rs756448450 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:798385 | CTTCTGACAACATCC[C/T]AAGAGCTTCACAACC | 7525 |
rs756534766 | snp | C/T | 1.65135e-05 | 0.00287341 | missense | YES1 | GRCh38.p7 | 18:751730 | TTATTTGAAATCTTT[C/T]ACCCTTCTTAAATGA | 7525 |
rs756538361 | snp | C/T | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723444 | CTCTCTGTTCATCTA[C/T]ATTCACCATGAGCAA | 7525 |
rs756556484 | in-del | -/AC/ACAC | | | intron-variant | YES1 | GRCh38.p7 | 18:786498 | TTAATAAGTCCATAC[-/AC/ACAC]ACACACACACACACA | 7525 |
rs756626303 | snp | C/T | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722429 | GAATTTCGAATCTGA[C/T]GATTAAAATCAGGTA | 7525 |
rs756666076 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:801742 | GAGAGAATATATAGA[C/T]TTCACAAACCCAAAC | 7525 |
rs756688866 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:747280 | TTTGAGACCAGCCTG[A/G]CCAATAGGCGAAACC | 7525 |
rs756725830 | snp | A/G | 1.74336e-05 | 0.00295237 | intron-variant | YES1 | GRCh38.p7 | 18:739696 | CACATTTTAATTTAC[A/G]CTTTTAATTCAAATG | 7525 |
rs756767219 | in-del | -/TT | | | intron-variant | YES1 | GRCh38.p7 | 18:770269 | CCCGGCCCTTTTATC[-/TT]TTTTTTTTTTTTTTT | 7525 |
rs756784236 | in-del | -/TGTT | | | intron-variant | YES1 | GRCh38.p7 | 18:781538 | TGAATTGTCACTGCC[-/TGTT]TATTTCTATCCTTCT | 7525 |
rs756787886 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:754881 | TTATTGTCCAACCCT[C/T]TATAATGTAAGCTCC | 7525 |
rs756840042 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:732765 | TTTCCCCGCTTACAA[C/T]TCTGTTCCTAATAAA | 7525 |
rs756840931 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:755955 | ACGAAAGGTTGTCAA[A/C]AATCACTTCTTGCTA | 7525 |
rs756967446 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:800875 | AACAAAGGCTGGGTG[C/T]GGTGGCTCACGACTG | 7525 |
rs756981715 | snp | A/G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:769141 | ATAGGTATAATAGGC[A/G/T]GTACCATCTAGGTTT | 7525 |
rs757011860 | in-del | -/GTTT | | | intron-variant | YES1 | GRCh38.p7 | 18:806286 | CCTTACTAGAGACTA[-/GTTT]AACTTCAACTACAAT | 7525 |
rs757017349 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:764772 | GAGTCTCGTTCTGTC[A/G]CCCAGGCTGGAGTGC | 7525 |
rs757038970 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:763365 | ATGACAGCAGTTAGA[C/T]AAGTTATAAAACTAT | 7525 |
rs757097085 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:786220 | TGGTCTCCACACAGG[A/T]ATTACTCAAATCACC | 7525 |
rs757112019 | in-del | -/TT | | | intron-variant | YES1 | GRCh38.p7 | 18:787081 | GTGATACATACTGTC[-/TT]TTTTTTTTTTTTTTT | 7525 |
rs757131356 | in-del | -/TCTG | | | intron-variant | YES1 | GRCh38.p7 | 18:811405 | GCTTCTTAAAACAGC[-/TCTG]CCCCATGCCCAATAA | 7525 |
rs757184778 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:758892 | TCTATTCACTGTCTA[C/G]AGAAGCACTAATATA | 7525 |
rs757185763 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:789513 | ACTTGAGCTCAGGAG[G/T]TCAAGGCTGCAATGA | 7525 |
rs757215837 | snp | C/T | 0.000144328 | 0.00849371 | intron-variant | YES1 | GRCh38.p7 | 18:737001 | ACAAGACATACGATA[C/T]AAAGGGAAGCAGAGA | 7525 |
rs757217630 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:787723 | TCAAAAAAAAAAAAA[-/T]ATTCTGTTGAATTAT | 7525 |
rs757234725 | snp | C/T | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776048 | ACGCATGTATGCATA[C/T]TCTACTGGATGTAAC | 7525 |
rs757308799 | snp | A/C/G | 3.3028e-05 | 0.00406363 | missense | YES1 | GRCh38.p7 | 18:724621 | GTTCTAATACTTCAC[A/C/G]GTTCACCATACCTAA | 7525 |
rs757340035 | snp | C/G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:736520 | ACTGAGAACCTCTGG[C/G/T]CTTTCTAGGAAAGAA | 7525 |
rs757380529 | snp | C/T | 8.4156e-05 | 0.00648621 | missense | YES1 | GRCh38.p7 | 18:736934 | GAATATAGTTCATTC[C/T]TTCAATATATGCCAT | 7525 |
rs757384203 | snp | A/G | 2.15636e-05 | 0.00328349 | intron-variant | YES1 | GRCh38.p7 | 18:756878 | GTCAGTTAACACACA[A/G]GATACTTCAAAAAGA | 7525 |
rs757402912 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:799548 | AATCCCATCTTTACT[A/G]AAAATACAAAAAGTA | 7525 |
rs757434615 | snp | C/T | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724262 | ATTAGAGTTTAATAC[C/T]TGGGGAAAAAAAAGT | 7525 |
rs757486067 | in-del | -/TTT | | | intron-variant | YES1 | GRCh38.p7 | 18:730344 | AAGGACCCAAGAGGA[-/TTT]TTTTTTTTTTTTTTT | 7525 |
rs757514271 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:790939 | CTATATTCATTCATT[A/C]ATTCAAAAAAATATT | 7525 |
rs757517420 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:780937 | ATGGTCCAGCCCCCT[C/T]TTTCTCCCAATATAA | 7525 |
rs757532089 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:746189 | AAAATACAGGAAAAT[A/G]TAAGAGTTTTATTGA | 7525 |
rs757540447 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:767761 | GCTGGAGTACAGGGG[C/T]ACGATCTCGGTTCAC | 7525 |
rs757567950 | in-del | -/TATATATATATATATATATATATATATATATATA | | | intron-variant | YES1 | GRCh38.p7 | 18:765249 | GGAAAGAGTTACAAC[lengthTooLong]TATATATATATCTGT | 7525 |
rs757571962 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:795178 | TAGGTAACTGTATTA[C/T]ACTGATGTTGAACTT | 7525 |
rs757624791 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:791427 | TACTAACACATTTAA[C/T]CCTTACAACCACCCT | 7525 |
rs757648763 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:782726 | TTTACATAGAGTCTC[A/G]TTCTGTCACCCAGGT | 7525 |
rs757725375 | in-del | -/C | | | intron-variant | YES1 | GRCh38.p7 | 18:749858 | AGCAAGACTCCGTCT[-/C]AAAAAAAAAAAAAAA | 7525 |
rs757731300 | snp | A/C | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813861 | GGCTCACACGTGTAA[A/C]CCCAGCATTCTGGGA | 7525 |
rs757753816 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:805351 | GATACAGTAATTACA[A/C]AGTATAAAAAAATAA | 7525 |
rs757760862 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:761601 | CACACCTTTTCTCCT[C/T]ACCCTATCAAGTCTT | 7525 |
rs757767673 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:791649 | AAAAACATAAAACAG[-/A]AAGAGATTAATTTTA | 7525 |
rs757787317 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:790633 | ATTTGAAAAGAAAGT[A/G]ATAACTTTGTATAAC | 7525 |
rs757806784 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:806839 | TCCTTCCTCTGGTTA[C/T]ACAAGTTTGAGCACT | 7525 |
rs757839221 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:728338 | AAAAAAAAAAAAATT[C/T]ATTTATGTTTCATAT | 7525 |
rs757855393 | snp | A/G | 1.64781e-05 | 0.00287033 | synonymous-codon | YES1 | GRCh38.p7 | 18:724589 | AGGGCACGGCATCCT[A/G]TATCCTCGCTCCACT | 7525 |
rs757867014 | snp | A/T | 1.64827e-05 | 0.00287073 | missense | YES1 | GRCh38.p7 | 18:724467 | GGCTCTGTAGCAGTG[A/T]AGTAGTCTTCCAAGA | 7525 |
rs757945173 | snp | C/G | 1.67265e-05 | 0.00289188 | missense | YES1 | GRCh38.p7 | 18:745710 | AATATTCACATACCT[C/G]TGTAGTGTTTCACCA | 7525 |
rs757952742 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:741022 | CGTGCCTCAGCCTCC[C/T]GAGCAGCTGGAACTA | 7525 |
rs758007811 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:727907 | TTCCTGCGTAGATAA[C/T]ATATAGGCTGAGTAT | 7525 |
rs758075463 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:809785 | AACAACAACAAATTC[A/T]TGTAAAATAAAACAT | 7525 |
rs758097592 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:801873 | GATTGGGAAAACATG[C/T]TCTGTTAATCTGGCG | 7525 |
rs758148242 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:766460 | CATGATTAGTGAAAG[A/C]TGATTATCTTTTCTA | 7525 |
rs758157945 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:798550 | TGAGAAGATGCATAG[A/G]GGAGCCGCTTTAGCT | 7525 |
rs758205413 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:751081 | ATATTTTATGTTCCG[C/G]AACAATAACTGGTAG | 7525 |
rs758250803 | snp | G/T | 3.88689e-05 | 0.00440828 | intron-variant | YES1 | GRCh38.p7 | 18:756858 | GACAATAAAATATTT[G/T]GAGAGTCAGTTAACA | 7525 |
rs758303637 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:792548 | CTCTCTCTCTCTCTC[-/T]CTCTCTCCCTCTGTA | 7525 |
rs758304599 | snp | A/G | 4.94222e-05 | 0.00497078 | stop-gained | YES1 | GRCh38.p7 | 18:743320 | GTCGCAAAGATTCTC[A/G]AGGGATTTCCCAAGC | 7525 |
rs758315112 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:735444 | AGTGGGGCTAAGCTA[C/T]GAGGACACAAAGGCA | 7525 |
rs758348096 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:792059 | CTGTTCTATGCTTTT[C/G]TACTAAAAAAAATAG | 7525 |
rs758374764 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:809032 | TAGGATCTTGATGCC[C/G]TAATTGAGTTTTGAG | 7525 |
rs758378120 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:764846 | CATGCGATTCTCCTG[A/C]CTCAGCCTCCCGAGT | 7525 |
rs758401112 | snp | C/T | 3.29468e-05 | 0.00405861 | missense | YES1 | GRCh38.p7 | 18:747990 | TCTTTCCTGTAGCGA[C/T]TGATCTTGCTTCCCA | 7525 |
rs758409901 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:778925 | GAAATGTTAGCAATG[C/G]ACAACTGATCTTGCA | 7525 |
rs758448968 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:807056 | AGGTGGACTGCTGGA[G/T]CCTAAGAATTTGAGA | 7525 |
rs758465731 | snp | C/T | 1.65416e-05 | 0.00287586 | intron-variant | YES1 | GRCh38.p7 | 18:733012 | TTTTTTAAAAATCTA[C/T]TTGTGTAAACATAGC | 7525 |
rs758470037 | in-del | -/TGGA | 1.64735e-05 | 0.00286993 | frameshift-variant, intron-variant | YES1 | GRCh38.p7 | 18:732834 | AAATGCAAGCTTACC[-/TGGA]TGGATATGGCACTCG | 7525 |
rs758483762 | snp | A/G | 2.19411e-05 | 0.00331211 | intron-variant | YES1 | GRCh38.p7 | 18:746067 | CTGGAAAAAAATTAA[A/G]TGTTTTGAATTGAAA | 7525 |
rs758510836 | snp | A/G | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775606 | GTTTGAGACCACCCT[A/G]AGCAACATAATGAGA | 7525 |
rs758513928 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:784225 | CAAGTTTTCTATATG[C/T]TCACCATATTAAAAT | 7525 |
rs758560267 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:811638 | AGTAAAGCCAGAAAG[C/G]CTCATCCACTCGCCC | 7525 |
rs758562178 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:763078 | AAGAATGAAAAGTGT[A/G]CAGAATGGCTCAGAT | 7525 |
rs758582813 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:805725 | ATTATTTTTAAAGTA[G/T]CCTTATCTGTAAAAT | 7525 |
rs758640021 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:769242 | TGTCTTTAAAGTGAC[A/G]TGCGACCGTAAGTAA | 7525 |
rs758664744 | snp | C/G | 1.6501e-05 | 0.00287232 | missense | YES1 | GRCh38.p7 | 18:736883 | TGCACACAAGATTTT[C/G]TCCTACAAGAATATT | 7525 |
rs758709210 | snp | C/T | 5.35404e-05 | 0.00517371 | missense | YES1 | GRCh38.p7 | 18:742921 | ACTAATACATACCTT[C/T]TGACATAAATTCAGT | 7525 |
rs758752228 | in-del | -/G | | | intron-variant | YES1 | GRCh38.p7 | 18:728462 | CTGTCACATGAGGAC[-/G]GGTGTGGAATTTTCC | 7525 |
rs758773950 | snp | C/G | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812745 | CTGTTCCTTGGCCCA[C/G]CTCTCAGTAGTGGCC | 7525 |
rs758790818 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:770736 | CAGTCCTGCACTGCT[A/G]TTGTCCAAAGTCTAA | 7525 |
rs758907124 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:730631 | CTTATGCTTTCTGTC[A/T]GGGTTTTACTGCCCT | 7525 |
rs758971721 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:765693 | GTGAGCCACCGCACC[C/T]GGCCAATTTAACACT | 7525 |
rs759026578 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:761078 | ATAAGAAGATACCTT[C/T]TGTGGTTACCAGACT | 7525 |
rs759045691 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:806463 | TATTAAGCTAGTTTT[A/G]TAACATTTTAGTAGA | 7525 |
rs759058483 | snp | A/G | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722810 | TTTAGAAGTGAATGT[A/G]GGCTGGGCGCGGTGG | 7525 |
rs759084064 | in-del | -/AAAAAA/AAAAAAA | | | intron-variant | YES1 | GRCh38.p7 | 18:735161 | ACTGTGTCTCAAAGC[-/AAAAAA/AAAAAAA]AAAAAAAAAAAAATC | 7525 |
rs759122264 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:794885 | GCAGTGGTGCAATCT[C/T]GGCTCACTGCAACCT | 7525 |
rs759141008 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:811092 | TAAAATTATCAAGGT[-/A]TCTTTGGCACTGTAA | 7525 |
rs759160553 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:805179 | CACTCTAGAGTGTAC[C/T]TACACAAACCTACGT | 7525 |
rs759164721 | snp | A/C | 1.76238e-05 | 0.00296843 | intron-variant | YES1 | GRCh38.p7 | 18:745663 | TTTTGTCCTCATAAA[A/C]TAGAATATGAAGAAA | 7525 |
rs759171685 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:740751 | ATCTCTCCCGCCTGG[-/A]AAATAATTGTACCCA | 7525 |
rs759189339 | snp | C/T | 1.64953e-05 | 0.00287182 | synonymous-codon | YES1 | GRCh38.p7 | 18:736872 | GTCTGCTATTTTGCA[C/T]ACAAGATTTTCTCCT | 7525 |
rs759222619 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:768888 | TTGTATTTTTAGTAG[A/G]GACAGGGTTTCCCCA | 7525 |
rs759251581 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:773729 | GTTCCAACTTTCCTA[C/T]GTTTCTCGCATTCAC | 7525 |
rs759257414 | snp | C/T | 1.64798e-05 | 0.00287047 | intron-variant | YES1 | GRCh38.p7 | 18:748061 | CAAGGTAGACTATTG[C/T]CCAAGGTACAATATA | 7525 |
rs759261504 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:811895 | GCAGGTCTGGACAGG[A/G]CAGAGACCGAGTCAG | 7525 |
rs759275449 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:754413 | ATTCTCACTTATCAA[A/G]TATCAGCTCAAGGCT | 7525 |
rs759403483 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:744533 | TAGCTGAGCCTACAG[A/G]TGCATGCCACCACGC | 7525 |
rs759485031 | in-del | -/TAAAG | | | intron-variant | YES1 | GRCh38.p7 | 18:777988 | ACAGTGTTACACTGT[-/TAAAG]TATTTTGCTTTAATA | 7525 |
rs759504367 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:778426 | CCTGTCAGCATGACA[A/T]TGTTGCCTTATTATT | 7525 |
rs759509528 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:767494 | CTAGTTCTCCTAGTA[C/T]AATTTGTTGAAAAAC | 7525 |
rs759521052 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:743590 | GCAAAACATGAAATA[C/T]ACATAAGTGAAACAT | 7525 |
rs759559464 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:765682 | GGATTACAGGCGTGA[C/G]CCACCGCACCCGGCC | 7525 |
rs759573463 | snp | A/G | 1.83316e-05 | 0.00302745 | intron-variant | YES1 | GRCh38.p7 | 18:736977 | CTTGGAAAGAGAAAA[A/G]CAAAAAACACAAGAC | 7525 |
rs759586588 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:810170 | CATAGTAGTAAATCA[-/T]TTACTGTCTAACATG | 7525 |
rs759599697 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:769518 | CTTAAGAGGAAAGTA[C/T]TTAGTCCATCACTAT | 7525 |
rs759600003 | snp | C/T | 1.64925e-05 | 0.00287158 | missense | YES1 | GRCh38.p7 | 18:743275 | CCATCCACACTTCGC[C/T]GAAACATCCTTGTCC | 7525 |
rs759601009 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:728751 | GGATGGTCTCAAACC[C/T]CTGACCTCGTGATCC | 7525 |
rs759605742 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:781950 | TTTTATAAACATTAT[C/T]GGAGTGCCTCATGGA | 7525 |
rs759611102 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:752680 | GGTCACAGTGGTTCA[C/T]GTCTGTAATCTCAGC | 7525 |
rs759673843 | in-del | -/GAG | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812605 | AGGCCGAGGGGGCGT[-/GAG]GAGGAGGTGCTTCCC | 7525 |
rs759738326 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:741731 | TCGCTTGAGCCCAGG[A/G]AGGTCCAAGCTGCAG | 7525 |
rs759781831 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:800370 | CACGGAGCTTACATT[A/C]CAGTGGCAGCCATTC | 7525 |
rs759815803 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:791827 | TGGGAGGCTGAGGCA[C/G]GTGGATTACTTGAGG | 7525 |
rs759877624 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:736798 | AGCTTTTATGTAAAA[A/G]TAATTTTACCTTGTC | 7525 |
rs759905906 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:786236 | ATTACTCAAATCACC[A/G]GGACTCAAAAGATAG | 7525 |
rs759911555 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:772694 | GCCTCGGCCTCTCAA[A/C]GTGCTGGGATTACAA | 7525 |
rs759936721 | snp | A/T | 3.29462e-05 | 0.00405857 | synonymous-codon | YES1 | GRCh38.p7 | 18:756597 | TGGCACCACTGAAAA[A/T]GAGGAAGATGCACCT | 7525 |
rs759965945 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:735038 | GGCAGGTGCCTGTAA[C/T]CCCAGCTACAGGGGA | 7525 |
rs759966083 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:751579 | AGAAGCCAATGCATC[A/G]TTAAACACAGTGGGC | 7525 |
rs759966349 | in-del | -/AG | | | intron-variant | YES1 | GRCh38.p7 | 18:793066 | TTTTTTTTGAGACAG[-/AG]TCTCACTGTGTCACC | 7525 |
rs759980529 | in-del | -/AAGAAAAAAAA | | | intron-variant | YES1 | GRCh38.p7 | 18:791249 | GAGTGAAACTTGAAG[-/AAGAAAAAAAA]AAGAAAAAAAAAAAA | 7525 |
rs760017110 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:736077 | CTCAGGAGGCTGAGG[C/T]GGGAGGATCACCTGA | 7525 |
rs760048255 | snp | A/G | 1.74974e-05 | 0.00295776 | missense | YES1 | GRCh38.p7 | 18:736960 | GCCATACCATCAGCA[A/G]TCTTGGAAAGAGAAA | 7525 |
rs760104975 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:809583 | TGGGATTACAGGTGT[C/G]AGCCACCGTGCCCAG | 7525 |
rs760209418 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:787962 | AACTGCTTTAGCCTC[A/G]AAATGTCCAGGTAAG | 7525 |
rs760210347 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:748085 | CAATATATTGCAGTG[C/T]TATCTTGTATCTGAA | 7525 |
rs760267714 | snp | C/T | 1.65351e-05 | 0.00287528 | missense | YES1 | GRCh38.p7 | 18:736828 | CTTGCTGTGTATTCA[C/T]TGTCTTCAATTAACC | 7525 |
rs760278526 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:783534 | GAGAAAAAAGTGAGA[A/G]GTCTGTAAGCTCATA | 7525 |
rs760297350 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:794982 | CACCATGCCTGGCTA[A/G]TTTTTGTATTTTTAG | 7525 |
rs760358376 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:726249 | GCCAACATGGTGAAG[C/T]CCCGTCTCTACTAAA | 7525 |
rs760359350 | snp | C/G/T | 6.6471e-05 | 0.00576469 | missense | YES1 | GRCh38.p7 | 18:756806 | CTGGACTTTTGTTTT[C/G/T]TTTACTTTTAATGCA | 7525 |
rs760369566 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:761064 | AAGAAATGCACATTA[C/T]AAGAAGATACCTTTT | 7525 |
rs760385335 | snp | A/G | 1.75029e-05 | 0.00295823 | synonymous-codon | YES1 | GRCh38.p7 | 18:746018 | CAAAAGTAATCTTTC[A/G]GCATCTTTTCTCCCC | 7525 |
rs760403863 | snp | C/G | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812793 | TTTTGTGGGGGAGGA[C/G]GGGGTTGAGTTTTTT | 7525 |
rs760412976 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:807539 | CAAAAGATGCGACTG[C/T]TGCTATTTGCTTGGC | 7525 |
rs760463202 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:744641 | GTGATCTGTCTGTTT[C/T]GGCCTCCCAAAGTGG | 7525 |
rs760470971 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:732705 | GTAAAGGGAAGGAGT[C/G]GGGAGAGGGAGAGGC | 7525 |
rs760513767 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:771529 | TTAAACCACTCCGTG[G/T]CATTTTTCTTTTACA | 7525 |
rs760541552 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:758015 | CTGTTGTATTCTGTC[C/T]ATACCAGGACTATGT | 7525 |
rs760542366 | snp | A/G | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724141 | TTTATAAATAAGCAG[A/G]AGCCTCACTGTCCTT | 7525 |
rs760577359 | snp | A/G | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813615 | GAACGAAAGGTAGGC[A/G]TAGGCGTTAAAGAGA | 7525 |
rs760626800 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:810706 | CGACTTTTAGCTAAT[A/G]TCCAAAAATAAAAAT | 7525 |
rs760669400 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:731532 | AAAACAGTTTTTCCT[A/G]AAGATTAAATTTTAT | 7525 |
rs760691863 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:752017 | AACTCAATAACTGGT[A/G]GCAATAACTAGTCTT | 7525 |
rs760714905 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:767447 | TAAGCCACAATGCCC[A/G]GCCCCATGTTCAATT | 7525 |
rs760763070 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:770178 | TTAGCCAGGATTGTC[A/T]TGATCTCCTGACGTC | 7525 |
rs760764868 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:784651 | GCTTGTGGGGGCTGC[C/T]CACATTCCTTGGCTC | 7525 |
rs760775133 | snp | A/G | 1.86458e-05 | 0.00305328 | intron-variant | YES1 | GRCh38.p7 | 18:742886 | TTAAAAACATTATCA[A/G]CACAAATACCTAAGG | 7525 |
rs760791614 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:799329 | AAACTATTTTTTCCA[A/G]CTCTCCTTACACTCA | 7525 |
rs760846787 | in-del | -/ATT | | | intron-variant | YES1 | GRCh38.p7 | 18:793032 | TTCATTATAATTATT[-/ATT]ATTATTATTGGTTTT | 7525 |
rs760896607 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:729901 | ATGTGTTGGGATTAC[A/G]GGCGTGAGCCACAGC | 7525 |
rs760944134 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:766151 | TGCCAAGTCCTTCAG[A/G]GGAGGCTCAGTGCCT | 7525 |
rs760958803 | snp | A/G | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775158 | TTGTGAAGATTAAAT[A/G]AGTAAATATATACAT | 7525 |
rs760968620 | snp | C/T | 3.39403e-05 | 0.00411934 | intron-variant | YES1 | GRCh38.p7 | 18:724681 | GGTCCTAACTACCAC[C/T]AGGAAAACATAACAA | 7525 |
rs761001547 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:750721 | GGGATAAGGACTGGG[C/T]CAGGCAGGGGAGGAA | 7525 |
rs761025054 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:809746 | GCACCTTATATAGAC[A/G]TTACACACTGGATTC | 7525 |
rs761071355 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:773871 | GAATCTTGCTCTGTC[A/G]CCCAGGCTAGAGTGC | 7525 |
rs761078282 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:788904 | GCACTCCAGCCTGGA[G/T]GACAGAGTTAAAGAT | 7525 |
rs761091434 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:737627 | GTGATAAAGGTATTA[A/T]CCACAAGGTATAGGT | 7525 |
rs761113379 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:738955 | CAGCCTCCTGAGTAG[C/T]TGGGATTACAGGCGC | 7525 |
rs761125985 | in-del | -/AT | 0.000176358 | 0.0093887 | intron-variant | YES1 | GRCh38.p7 | 18:745658 | ATGGATTTTGTCCTC[-/AT]AAACTAGAATATGAA | 7525 |
rs761166206 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:725347 | GTCAGGCCATCCCTT[C/G]TATCTCTTGGAAACT | 7525 |
rs761306136 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:787770 | CATCATTTAGGACCT[G/T]ACCCAAATGATAAAT | 7525 |
rs761307060 | snp | A/T | 1.73186e-05 | 0.00294261 | intron-variant | YES1 | GRCh38.p7 | 18:751854 | TAGCTAACTTAACAA[A/T]ACAGAAAAAAAGAAC | 7525 |
rs761308729 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:748460 | TATATTTACAGAGTT[C/G]TACAACCATTATCAC | 7525 |
rs761335962 | snp | A/C | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813741 | TCAGCTTTTATTAAA[A/C]TAGAAAATTCCTTGA | 7525 |
rs761343104 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:785020 | TCAACTGTTAGGGTT[C/G]AGAGAGTCAGTATGC | 7525 |
rs761347968 | snp | C/T | 1.64743e-05 | 0.00287 | missense, intron-variant | YES1 | GRCh38.p7 | 18:732951 | GAGCTGTCCATTTGA[C/T]TGGAAATTTTGCACC | 7525 |
rs761377693 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:750502 | CTCACTAGAAGACAG[C/T]GGCAGCACCCCAACT | 7525 |
rs761398374 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:771611 | TGGAGTGCAGTGGCG[C/T]GATCACGACTCACTG | 7525 |
rs761417327 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:783767 | ATTACAGGCGCTGCC[A/T]CCATGCCCAGCTAAT | 7525 |
rs761446313 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:796683 | GAATCACTTGAACCC[A/G]GGAGGTGGAGGTTAC | 7525 |
rs761463934 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:791920 | ATCAGCTGGGGGTGT[C/T]GGCGTGCACCTGTGA | 7525 |
rs761477770 | in-del | -/TT | | | intron-variant | YES1 | GRCh38.p7 | 18:793043 | TATTATTATTATTGG[-/TT]TTTTTTTTTTTTTTT | 7525 |
rs761496984 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:790154 | ACCAAGGTGGGCGGA[A/T]CACCTGAGGTCAGAA | 7525 |
rs761544020 | snp | C/T | 1.88425e-05 | 0.00306935 | intron-variant | YES1 | GRCh38.p7 | 18:742870 | ATACAAATCAAGACT[C/T]TTAAAAACATTATCA | 7525 |
rs761599814 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:778664 | CCTAGAAAAATAAAT[C/T]TAGAGACTTAACTTC | 7525 |
rs761617938 | snp | A/G | 1.711e-05 | 0.00292484 | intron-variant | YES1 | GRCh38.p7 | 18:736784 | CACAACACATTACAA[A/G]CTTTTATGTAAAAGT | 7525 |
rs761748148 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:801155 | CATCTCAAAAAAATA[C/T]AAAAATAAAAAATAA | 7525 |
rs761749668 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:749447 | AGTTTGCAGTCAGCC[A/C]AGATCATGCCATTGC | 7525 |
rs761809134 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:803040 | TTAAGATCAGTCTGA[C/G]CAACATGGTGAGAAA | 7525 |
rs761834097 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:737752 | TGAGACGGGGTCTCA[C/T]TCTGTCACGCAGGTT | 7525 |
rs761847874 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:788448 | TGTACATAATAACGA[C/T]GTGTATATATTTAAA | 7525 |
rs761855510 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:753863 | TTTCTCCTCTAACCT[A/G]TATTTACATACCCAA | 7525 |
rs761930900 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:787862 | ACTGATATTAATCCA[C/T]AGATCGACATATATC | 7525 |
rs761948180 | snp | A/T | 0.000100963 | 0.0071043 | intron-variant | YES1 | GRCh38.p7 | 18:751847 | AATTATGTAGCTAAC[A/T]TAACAAAACAGAAAA | 7525 |
rs761978136 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:793150 | GTTCAAGCGATACTC[C/T]TGCCTCAGCCTCCCA | 7525 |
rs761985717 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:789166 | ACAGAACATATGCTA[C/T]AAAACCTAAGGAAAT | 7525 |
rs762101167 | snp | C/T | 1.75795e-05 | 0.0029647 | intron-variant | YES1 | GRCh38.p7 | 18:743453 | CTGTAATATCAATTA[C/T]AAAAATTAAGGGGCA | 7525 |
rs762103169 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:807715 | AGGAAAAGAATGCAG[A/T]GTTCCTACTAGCAAA | 7525 |
rs762110859 | in-del | -/T | 1.86745e-05 | 0.00305563 | intron-variant | YES1 | GRCh38.p7 | 18:745932 | ATACTTATACTAATA[-/T]TAACAATATTCATAC | 7525 |
rs762131756 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:800535 | TTAAGCTAGTATTCC[C/T]GCTAGAAAACAATGT | 7525 |
rs762171465 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:725604 | TCTTCATAAGTGAAA[A/T]CTGGCCGGGCACAGT | 7525 |
rs762172228 | snp | C/T | 1.67464e-05 | 0.0028936 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724419 | TATAAAATAGGCTAC[C/T]TGAATTATAAATTTT | 7525 |
rs762187395 | snp | A/C | 1.64768e-05 | 0.00287021 | stop-gained | YES1 | GRCh38.p7 | 18:743302 | GTCCTAGTTTAACCT[A/C]TAGTCGCAAAGATTC | 7525 |
rs762203292 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:762800 | ATATTAGACACTGTA[A/G]AAGGAGCTGGGAGGA | 7525 |
rs762268461 | snp | C/G | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722832 | GCGCGGTGGCTCACG[C/G]CTGTAATCCCAGCAC | 7525 |
rs762309055 | in-del | -/TC | | | intron-variant | YES1 | GRCh38.p7 | 18:809381 | CTTAGCTCACCGCAA[-/TC]TCTGTCTCCCGGGTT | 7525 |
rs762310761 | in-del | -/CTGACTTACTAGTTC | | | intron-variant | YES1 | GRCh38.p7 | 18:742176 | CTGTCAGCTTATCTG[-/CTGACTTACTAGTTC]CTCTAAGTACCATCT | 7525 |
rs762319590 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:740225 | CTGTGGAACTACTGC[C/T]GTGACCAAGCTCTCT | 7525 |
rs762365121 | snp | A/G | 1.64765e-05 | 0.00287019 | missense | YES1 | GRCh38.p7 | 18:724576 | CTGGACAGCCCTGAG[A/G]GCACGGCATCCTGTA | 7525 |
rs762372329 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:780369 | ACTAAAGGATAAATG[C/G]ATTCATGGGTCATCA | 7525 |
rs762456140 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:782817 | CTTGTGCCTCAGGCT[C/G]CCAAGCACCTGGGAT | 7525 |
rs762482598 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:745863 | GAATAAGCACCTGGG[A/T]GAAAAATAAATACTT | 7525 |
rs762488667 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:803941 | AGGCCAAAAGGCTTA[C/T]GTTACAGAAAAGACT | 7525 |
rs762507547 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:783006 | AATTTCTGATCTCAA[C/T]AGCTAATGCTGCAAA | 7525 |
rs762515943 | snp | C/T | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722447 | TTAAAATCAGGTAAA[C/T]AATGATAGTTAAGAA | 7525 |
rs762519747 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:735820 | GTTTCCCAAAAACTA[C/T]TGAAAAAAAAAGTGG | 7525 |
rs762542579 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:759623 | GACTTTTTTTCCTTG[C/T]CATTATTCCCTAAAC | 7525 |
rs762566113 | snp | C/T | 4.94287e-05 | 0.00497111 | intron-variant | YES1 | GRCh38.p7 | 18:732800 | TGATAAAGCCACTCA[C/T]GAGATAACCAAGAGC | 7525 |
rs762568053 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:771684 | CTCTCTAGTAGCTGG[G/T]ACCACAGGTGCAGGC | 7525 |
rs762569020 | snp | C/T | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722934 | CGTCTCTACTAAAAA[C/T]ACAAAAAACTAGCCA | 7525 |
rs762636176 | snp | A/C | 1.64735e-05 | 0.00286993 | missense, intron-variant | YES1 | GRCh38.p7 | 18:732939 | GTGCAGCTTCAGGAG[A/C]TGTCCATTTGATTGG | 7525 |
rs762638947 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:745555 | AAGTACTAAGTATTA[C/T]CTGTTCCTCCCTTTA | 7525 |
rs762650247 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:786108 | CTTTATAAATTACCA[A/G]ATCTGTGGTACTGTT | 7525 |
rs762678626 | snp | A/G | 1.68476e-05 | 0.00290233 | missense | YES1 | GRCh38.p7 | 18:739761 | TATCAACCAGCTGTG[A/G]AAGCTTCAAATACTT | 7525 |
rs762695937 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:786338 | TCTTCCTCCCTAGAG[-/T]TAGGAGGAAGGGGAG | 7525 |
rs762751679 | snp | C/G | 1.75523e-05 | 0.00296241 | missense | YES1 | GRCh38.p7 | 18:745972 | TTTCACTCTCTCTTA[C/G]TAAGAAAATACCTCG | 7525 |
rs762766824 | snp | A/G | 4.03722e-05 | 0.00449272 | intron-variant | YES1 | GRCh38.p7 | 18:736997 | AAACACAAGACATAC[A/G]ATACAAAGGGAAGCA | 7525 |
rs762769164 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:794772 | CTCTGTTGTCACAAG[A/G]CATTCTCTCTGGGTG | 7525 |
rs762826295 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:729911 | ATTACAGGCGTGAGC[A/C]ACAGCGCCCAGCCAG | 7525 |
rs762845870 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:793242 | GACAGGGTTTCACCA[C/T]GTTGGCCAGGATGGT | 7525 |
rs762913729 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:744205 | AGGCCCTGCAGTTAG[C/T]AAATGGTAGAGATGG | 7525 |
rs762935976 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:746748 | TAAACTGGTTTAACC[C/T]AAAAGTAGTGTGTCA | 7525 |
rs762958362 | snp | C/T | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776569 | CATTCTTTAATTTTC[C/T]GTGTATTGGAGGAGT | 7525 |
rs762969267 | in-del | -/CAG | | | cds-indel | YES1 | GRCh38.p7 | 18:721637 | TGATTAAATTCTGCT[-/CAG]TAGTTACAAGTAACT | 7525 |
rs762972542 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:805085 | CAAACATTTCCTTAA[A/C]ATTTTATCAATACGG | 7525 |
rs763031879 | in-del | -/TG | | | intron-variant | YES1 | GRCh38.p7 | 18:792565 | CTCTCCCTCTGTATA[-/TG]TGTGTGTGTGTGTGT | 7525 |
rs763033271 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:751880 | GAACTATTGCCAGCC[-/A]AAAAAAAAAAAAGCT | 7525 |
rs763033395 | snp | C/G | 1.64757e-05 | 0.00287012 | synonymous-codon | YES1 | GRCh38.p7 | 18:724553 | ATTCATCAATTCATG[C/G]AGGGATTCTGGACAG | 7525 |
rs763057233 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:726601 | CCTGGCCAACATGGC[A/G]AAACCCCCTCTCTAC | 7525 |
rs763059287 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:741337 | TGGCCTTAACCTCCT[C/G]GGCTCAAGCAATCCT | 7525 |
rs763095168 | in-del | -/A | 6.12151e-05 | 0.00553207 | intron-variant | YES1 | GRCh38.p7 | 18:746056 | CAAAATACCATCTGG[-/A]AAAAAATTAAGTGTT | 7525 |
rs763147848 | snp | C/T | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813420 | TCTTTATTTCCTCTT[C/T]GGTGGGGTTATCAGA | 7525 |
rs763149862 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:768597 | CCATCATGTGCAGCG[-/T]TAACATTTTGGTCAA | 7525 |
rs763232008 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:799007 | TTACCACCTCAAATA[C/T]AAAATTAAATTAGTC | 7525 |
rs763236969 | snp | A/G | 1.65097e-05 | 0.00287308 | missense | YES1 | GRCh38.p7 | 18:756794 | TGTATTTAATGGCTG[A/G]ACTTTTGTTTTCTTT | 7525 |
rs763253103 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:798096 | CCTCACTCTGAGAAC[C/G]ACCTTCATGATCATG | 7525 |
rs763282872 | snp | A/C | 5.00989e-05 | 0.00500469 | intron-variant | YES1 | GRCh38.p7 | 18:751678 | TTTCTGTCAGTATTT[A/C]TCTCACAAAATATTC | 7525 |
rs763308490 | snp | G/T | 1.75946e-05 | 0.00296598 | intron-variant | YES1 | GRCh38.p7 | 18:743124 | ACACATTTTAGGAAT[G/T]TATATTTTAAAGGAT | 7525 |
rs763310037 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:785101 | ACCCTTTGAATGTGA[G/T]GACTATTTTGCTTAT | 7525 |
rs763332220 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | YES1 | GRCh38.p7 | 18:756691 | GCTGTTCCCTTTGCT[A/G]AAGATGACGGACATG | 7525 |
rs763335585 | snp | A/C | 5.15424e-05 | 0.00507627 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724408 | AGATTTGTGCATATA[A/C]AATAGGCTACTTGAA | 7525 |
rs763350144 | in-del | -/C | | | intron-variant | YES1 | GRCh38.p7 | 18:732457 | AAAAAAAAAAAAAAA[-/C]CAAAACACCAATCAC | 7525 |
rs763427480 | snp | C/G | 1.64792e-05 | 0.00287042 | missense | YES1 | GRCh38.p7 | 18:743293 | AACATCCTTGTCCTA[C/G]TTTAACCTCTAGTCG | 7525 |
rs763438852 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:750617 | TAACAAGCAAGTGAC[A/G]AATTGTAATTCAAAA | 7525 |
rs763448001 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:783743 | GCTTCAGCCACCCAA[G/T]TAGCTGGGATTACAG | 7525 |
rs763565902 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:808534 | ACTTATATTATAAAA[C/T]TGTTTAAATGTGAAC | 7525 |
rs763603006 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:733983 | CAAAATGTTTTATTT[A/T]AAAAGTGGCAGGTGG | 7525 |
rs763626061 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:764277 | GCCTAGGCTAGAGCA[C/T]AATGGTACAATCCCG | 7525 |
rs763630483 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:769083 | GACATGTTTGTAGCC[C/T]AGGAGCCATAGGCTA | 7525 |
rs763659084 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:801055 | GGAGGCTGAGGCAGG[A/C]GAATCGCTTGAACCA | 7525 |
rs763679841 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:796348 | TTGAAGGTTCTGTGA[A/G]AAATGAGTTAGCTAA | 7525 |
rs763702147 | in-del | -/ATAGGC | | | intron-variant | YES1 | GRCh38.p7 | 18:778785 | CATAAAGCACAAAGG[-/ATAGGC]AGGACCATAAAAGAG | 7525 |
rs763723640 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:746157 | GGACGACAAAGAATA[A/G]CTAGAGAACATGGCT | 7525 |
rs763734784 | in-del | -/AAG | | | intron-variant | YES1 | GRCh38.p7 | 18:786012 | ATGAGATAACACAGC[-/AAG]AAGAAGGCCCTTGCC | 7525 |
rs763762997 | snp | G/T | 1.69885e-05 | 0.00291444 | intron-variant | YES1 | GRCh38.p7 | 18:745870 | CACCTGGGTGAAAAA[G/T]AAATACTTTCACTAT | 7525 |
rs763774120 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:795091 | GGATGCTATTTCCAA[A/G]TAAGGCCACATTCAC | 7525 |
rs763786814 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:762752 | TTGTACCTCAAAAGC[A/T]ATCAAAATAAAACCA | 7525 |
rs763795278 | in-del | -/TG | | | intron-variant | YES1 | GRCh38.p7 | 18:737043 | TGGTTAATATCAAAT[-/TG]TGTCACTGAAAATCA | 7525 |
rs763832807 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:782681 | ATGTAAAAAGGATTA[C/T]TTTTTCTTTCTAATT | 7525 |
rs763841928 | in-del | -/GCG | | | intron-variant | YES1 | GRCh38.p7 | 18:812016 | CGGGGGCGGGGAACC[-/GCG]GCGGCGGCGGCGGCG | 7525 |
rs763879192 | snp | A/G | 0.000101635 | 0.0071279 | missense | YES1 | GRCh38.p7 | 18:739773 | GTGGAAGCTTCAAAT[A/G]CTTTCCATCTCCTTC | 7525 |
rs763927725 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:811586 | CAACCCAAAACAAAG[C/G]AAAACTTTAAACATG | 7525 |
rs763992642 | in-del | -/TTT | | | cds-indel | YES1 | GRCh38.p7 | 18:721765 | GCATTCAATGAGAAC[-/TTT]TTATTTCAATTATCC | 7525 |
rs764048271 | snp | C/T | 1.65792e-05 | 0.00287912 | intron-variant | YES1 | GRCh38.p7 | 18:751695 | CTCACAAAATATTCA[C/T]GACACTTACGTATTG | 7525 |
rs764108599 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:802897 | AGACAGCCTGGGCAA[A/C]AAGGTGAAACCCTGT | 7525 |
rs764109167 | snp | A/G | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722869 | AGGCCGAGGCGGGCA[A/G]ATCACAAGGTCAGGA | 7525 |
rs764168191 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:755882 | CCCTTTACAAAAGAG[C/T]TCATTTTCTCTCTTT | 7525 |
rs764174919 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:752030 | GTAGCAATAACTAGT[C/T]TTAAACTCTCCGAAG | 7525 |
rs764251649 | snp | C/G/T | 0.000264474 | 0.0114966 | intron-variant | YES1 | GRCh38.p7 | 18:736999 | ACACAAGACATACGA[C/G/T]ACAAAGGGAAGCAGA | 7525 |
rs764255222 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:750945 | TGGGTATTAGAGTTA[A/G]AAGAGGGGAGAAGCA | 7525 |
rs764289588 | snp | C/G | 8.23649e-05 | 0.00641683 | missense | YES1 | GRCh38.p7 | 18:747995 | CCTGTAGCGATTGAT[C/G]TTGCTTCCCACCAAT | 7525 |
rs764298111 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:761505 | TAATTGCCCAACTAC[C/G]TCAGTTTCCATTCCC | 7525 |
rs764369917 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:736313 | CTACCATTTTGGGCC[-/T]GATAATTCTGTTGTG | 7525 |
rs764377527 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:810818 | ATATATATTATTTGC[C/T]AAAGTAAAACTTTCT | 7525 |
rs764398229 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:752915 | GCCACTGCACTGTAG[C/T]CTGGGTGACACAGCA | 7525 |
rs764428060 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:799459 | TCACGCCTGTAATCC[C/G]AGCACTCTGGGAGGC | 7525 |
rs764433044 | snp | C/T | 1.76309e-05 | 0.00296903 | intron-variant | YES1 | GRCh38.p7 | 18:743127 | CATTTTAGGAATTTA[C/T]ATTTTAAAGGATTTT | 7525 |
rs764465168 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:749906 | TCCAGTAAGACCAAA[A/G]TTAAATGATAATTCA | 7525 |
rs764509251 | snp | A/G | 0.000132369 | 0.00813432 | synonymous-codon | YES1 | GRCh38.p7 | 18:756795 | GTATTTAATGGCTGG[A/G]CTTTTGTTTTCTTTA | 7525 |
rs764522302 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:728249 | GAGGATCACCTGAGC[A/C]CAGGGAGGTAGAGGC | 7525 |
rs764529213 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:773993 | CCCACCATCTTGCCC[A/G]GCTAATTTTTGTATT | 7525 |
rs764538489 | in-del | -/CA | | | intron-variant | YES1 | GRCh38.p7 | 18:792555 | CTCTCTCTCTCTCTC[-/CA]CCTCTGTATATGTGT | 7525 |
rs764561620 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:737688 | GCCTGCAGCCTGTTT[C/T]TGCACAGCCAGAGAA | 7525 |
rs764596865 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:805304 | CAACTGTAACAGTAT[G/T]TGTGTATTTAAACAT | 7525 |
rs764612230 | in-del | -/AG | | | intron-variant | YES1 | GRCh38.p7 | 18:741778 | TCCACCCTGGGGGAT[-/AG]AGTGAGGCCCCACCT | 7525 |
rs764659420 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:736466 | AGACATTGTCAGATG[C/T]CCCCTGGTGAGTGGC | 7525 |
rs764662846 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:787789 | CAAATGATAAATACT[C/G]ATCAAAAATTAATGT | 7525 |
rs764716556 | snp | C/T | 1.64754e-05 | 0.00287009 | missense | YES1 | GRCh38.p7 | 18:743317 | CTAGTCGCAAAGATT[C/T]TCGAGGGATTTCCCA | 7525 |
rs764750971 | snp | A/C | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723599 | CTTACTTTGCATGCT[A/C]TCTAAAGATCAAAAC | 7525 |
rs764777021 | snp | A/G | 1.76083e-05 | 0.00296712 | intron-variant | YES1 | GRCh38.p7 | 18:745665 | TTGTCCTCATAAACT[A/G]GAATATGAAGAAATA | 7525 |
rs764816566 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:785052 | TCCATACTAAGCAAC[A/G]TAACTGTTAAATTAG | 7525 |
rs764823798 | snp | C/T | 3.29538e-05 | 0.00405904 | missense | YES1 | GRCh38.p7 | 18:724583 | GCCCTGAGGGCACGG[C/T]ATCCTGTATCCTCGC | 7525 |
rs764836123 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:797865 | CCTTTCAGAACCTTG[A/G]GATATAATTCTTCTA | 7525 |
rs764880379 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:761551 | CCTCACCTCCTTTAC[C/G]CATAACCATCTTAAA | 7525 |
rs764919542 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:739374 | GCTGAGGTGGGAGGA[A/T]CCTTTGAGCCAAGGA | 7525 |
rs764942157 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:748486 | ATCACAATCAATTTT[A/G]GAATATTTTCATCAC | 7525 |
rs764949456 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:729904 | TGTTGGGATTACAGG[C/T]GTGAGCCACAGCGCC | 7525 |
rs764964636 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:770535 | AGTGTCCTTCCTGCT[C/G]AACTTTGCCCTACAA | 7525 |
rs765047662 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:737414 | GCCAAGATTGTGCCA[C/T]TGCACTCCAGCCTGG | 7525 |
rs765079894 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:743863 | GTGAGCCAAAATTGC[A/G]CCACTGCACTCTAGC | 7525 |
rs765080545 | snp | C/T | 1.64953e-05 | 0.00287182 | missense | YES1 | GRCh38.p7 | 18:736874 | CTGCTATTTTGCACA[C/T]AAGATTTTCTCCTAC | 7525 |
rs765082523 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:778762 | ATTTATAAATCCCCT[C/T]CCTTAAGCATAAAGC | 7525 |
rs765110261 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:764073 | TGCAGTGAGCCGAGA[C/T]CACACCACTGCACTC | 7525 |
rs765122899 | in-del | -/C | | | intron-variant | YES1 | GRCh38.p7 | 18:769439 | TACCTTATTCACTGA[-/C]TAGTACCTCCAGTGC | 7525 |
rs765124743 | in-del | -/C | | | intron-variant | YES1 | GRCh38.p7 | 18:778127 | AATCTCTACATTTTA[-/C]ATTTGAAGAAACTGA | 7525 |
rs765230889 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:791948 | TGAGCCCAGCTACTC[A/G]AAATCGGGTGTGTAT | 7525 |
rs765248264 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:737839 | ATTTTCCCACCTCAG[C/G]CTAGTGAGTAGCTGG | 7525 |
rs765257897 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:788454 | TAATAACGATGTGTA[C/T]ATATTTAAAATTTTG | 7525 |
rs765361420 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:725723 | TGAAACCACGACTCT[A/G]CAAACTACAAAAATG | 7525 |
rs765365787 | in-del | -/CACTTT | 1.64784e-05 | 0.00287035 | intron-variant | YES1 | GRCh38.p7 | 18:732793 | AACTCCTGATAAAGC[-/CACTTT]CACTCATGAGATAAC | 7525 |
rs765366963 | in-del | -/CTTA | 1.76786e-05 | 0.00297305 | frameshift-variant | YES1 | GRCh38.p7 | 18:745968 | GTTGTTTCACTCTCT[-/CTTA]CTAAGAAAATACCTC | 7525 |
rs765428158 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:752169 | CTGGAGTGCAGTGGT[A/G]TGATTTTGGCTTGCT | 7525 |
rs765479181 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:774401 | TTTAACTGTCTACGC[A/G]ATACCTTCACTTGGA | 7525 |
rs765484832 | snp | A/G | 1.79732e-05 | 0.00299771 | splice-donor-variant | YES1 | GRCh38.p7 | 18:742916 | GAGATACTAATACAT[A/G]CCTTTTGACATAAAT | 7525 |
rs765566848 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:788026 | ATATGAGAAAGGCAG[G/T]ATGCACGCTGACTGT | 7525 |
rs765607693 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon | YES1 | GRCh38.p7 | 18:756678 | GCTGAAATTAACTGC[C/T]GTTCCCTTTGCTGAA | 7525 |
rs765645233 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:796694 | ACCCGGGAGGTGGAG[G/T]TTACAGTGAGCCAAG | 7525 |
rs765691747 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:762893 | ATGTGAAAAATGCTA[C/G]AGTGTGACAAAATGT | 7525 |
rs765696495 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:806851 | TTATACAAGTTTGAG[C/T]ACTACTTTTCTCAAT | 7525 |
rs765718394 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:726561 | TGAGTGGGCGGATCA[C/T]CTGAGGTCAGGAGTT | 7525 |
rs765723765 | snp | A/G | 5.08083e-05 | 0.00504 | missense | YES1 | GRCh38.p7 | 18:743079 | TTGATTGCTACTTTC[A/G]TGGTTCCATTCCATG | 7525 |
rs765807073 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:754135 | TTCTCAAAAGAAAAT[A/T]CAATCAAATCCTTTA | 7525 |
rs765819770 | in-del | -/ATCTCT | | | intron-variant | YES1 | GRCh38.p7 | 18:792527 | ACACACTGAGACTCC[-/ATCTCT]CTCTCTCTCTCTCTC | 7525 |
rs765834475 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:757273 | CTTTGGGAGGCCAAG[A/G]CGGGCGGATCACGAG | 7525 |
rs765855267 | snp | A/G | 4.94173e-05 | 0.00497053 | missense | YES1 | GRCh38.p7 | 18:756700 | TTTGCTGAAGATGAC[A/G]GACATGGTGACACTG | 7525 |
rs765907620 | in-del | -/ACAAC/CAAC/CAACAAC | | | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721562 | CAAAACAAAACAAAA[-/ACAAC/CAAC/CAACAAC]AAAAAAGAAAATTGA | 7525 |
rs765960384 | snp | A/G | 1.64762e-05 | 0.00287016 | missense | YES1 | GRCh38.p7 | 18:743304 | CCTAGTTTAACCTCT[A/G]GTCGCAAAGATTCTC | 7525 |
rs765990923 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:771696 | TGGGACCACAGGTGC[A/G]GGCCATGATGCCTGG | 7525 |
rs766054485 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:772602 | CATGCCCAGCTAATT[C/T]TGTATTTTTAGTAGA | 7525 |
rs766055029 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:805088 | ACATTTCCTTAAAAT[G/T]TTATCAATACGGTCA | 7525 |
rs766059693 | snp | A/G | 3.295e-05 | 0.00405881 | missense | YES1 | GRCh38.p7 | 18:747947 | ATGGAATCTGCAGGC[A/G]CTACATAATTGCTCG | 7525 |
rs766109169 | snp | A/C | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722208 | AAGCCCTTAAAAAAT[A/C]TCATGTCACAAGTTG | 7525 |
rs766144960 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:803960 | ACAGAAAAGACTTCC[A/T]GGAAAAACAGATTCT | 7525 |
rs766169589 | snp | A/T | 1.65091e-05 | 0.00287303 | intron-variant | YES1 | GRCh38.p7 | 18:732992 | TTGACCATCTTGCTT[A/T]ATTGTTTTTTAAAAA | 7525 |
rs766182225 | snp | C/T | 1.6531e-05 | 0.00287493 | missense | YES1 | GRCh38.p7 | 18:736829 | TTGCTGTGTATTCAT[C/T]GTCTTCAATTAACCT | 7525 |
rs766187410 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:809813 | CATAGAAACAGATTC[C/T]GCACACAAACGTAGG | 7525 |
rs766218782 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:744373 | GAAAAAGTTCATTTA[C/G]GATCATTTAGGAGAT | 7525 |
rs766256748 | snp | C/T | 1.77881e-05 | 0.00298223 | synonymous-codon | YES1 | GRCh38.p7 | 18:746027 | TCTTTCAGCATCTTT[C/T]CTCCCCATTTTGCCA | 7525 |
rs766280503 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:739533 | GCTAGAGCCCAAGAA[G/T]TCAAGGCTCTTCAAG | 7525 |
rs766361048 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:780428 | GGAAGAGAGATCTTA[A/G]CTTAGCACAATAGCA | 7525 |
rs766385590 | snp | C/T | 1.64885e-05 | 0.00287123 | missense | YES1 | GRCh38.p7 | 18:745764 | GCTCTGGTTGTGATA[C/T]AGTATCCACCATTGT | 7525 |
rs766418371 | snp | C/T | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776926 | AACTTCCCCAACTTA[C/T]TTTTCTAATACGCTT | 7525 |
rs766464966 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:730148 | CTCCTAGGGTATGGA[C/T]TTTCTGGGGTCTCAA | 7525 |
rs766481034 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:789391 | GTTCAAGATCAGCCT[C/G]GGCAACATAGGGAGA | 7525 |
rs766504510 | snp | A/C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:763098 | ATGGCTCAGATGCTT[A/C/G]AAACAGCATGGTTCA | 7525 |
rs766516993 | in-del | -/A | 1.66078e-05 | 0.00288161 | intron-variant | YES1 | GRCh38.p7 | 18:747895 | AAAATCAAAATAATT[-/A]ATAAAATATGAAGTA | 7525 |
rs766532690 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:786237 | TTACTCAAATCACCA[A/G]GACTCAAAAGATAGA | 7525 |
rs766558139 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:802833 | CACACCTATAATCCT[A/T]GCACTTCGGGAGGTT | 7525 |
rs766599590 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:734292 | AGGCGCGGTGGCTCA[C/T]GCCTGTATTCCCAGC | 7525 |
rs766610930 | snp | C/T | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813254 | CTTTCCTATGAGCCT[C/T]GTAAAGCCAGTCGTT | 7525 |
rs766635490 | snp | C/T | 0.000372814 | 0.013648 | intron-variant | YES1 | GRCh38.p7 | 18:742887 | TAAAAACATTATCAA[C/T]ACAAATACCTAAGGA | 7525 |
rs766694477 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:797627 | AATAAAGCACTTCTA[A/G]ACAACTGTTAAAAAT | 7525 |
rs766798805 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:750706 | TACTTAATCCAGCAG[A/G]GGATAAGGACTGGGC | 7525 |
rs766886939 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:746105 | GGTTCAGAAAAATTA[C/T]ACAGAAGTGTCAGTA | 7525 |
rs766890180 | snp | C/T | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722017 | TACACATTAAGTTAG[C/T]GTTTTATCCCTACTA | 7525 |
rs766938995 | snp | A/G | 1.74366e-05 | 0.00295263 | synonymous-codon | YES1 | GRCh38.p7 | 18:739798 | TCCTTCCTTAAGGAA[A/G]TCTAATAAGCTTCCT | 7525 |
rs766940140 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:731750 | AGGCGGGCAGATCAC[A/G]AGGTCAGGAGATCGA | 7525 |
rs766967664 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:732473 | CAAAACACCAATCAC[A/G]CTACTGGGAAAGAAC | 7525 |
rs766984952 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:798302 | TCTAGCTATAAATTT[A/C]TCTCTAAGAATCATC | 7525 |
rs767020150 | in-del | -/AC/ACAG | | | intron-variant | YES1 | GRCh38.p7 | 18:786538 | CACACACACACACAG[-/AC/ACAG]AGTTGCTCCTCATTA | 7525 |
rs767026943 | snp | C/T | 1.73435e-05 | 0.00294473 | intron-variant | YES1 | GRCh38.p7 | 18:751856 | GCTAACTTAACAAAA[C/T]AGAAAAAAAGAACTA | 7525 |
rs767030803 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:748840 | TTCCTGTAGCCAGAC[A/C]ATTAACAATGAGCAA | 7525 |
rs767031283 | in-del | -/TA | | | intron-variant | YES1 | GRCh38.p7 | 18:759777 | TGCAGGTTACATATG[-/TA]TATACATGTGCCATG | 7525 |
rs767039662 | in-del | -/TC | | | intron-variant | YES1 | GRCh38.p7 | 18:782028 | ATTTGGTTCATTTCT[-/TC]TCTGTTTCTCCTGGT | 7525 |
rs767079230 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:806508 | ATTTGTTTTGTTTGC[A/G]AAAAGTCCATAGCTG | 7525 |
rs767099976 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | YES1 | GRCh38.p7 | 18:756697 | CCCTTTGCTGAAGAT[A/G]ACGGACATGGTGACA | 7525 |
rs767144855 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:773738 | TTCCTATGTTTCTCG[A/C]ATTCACTTAAAATAC | 7525 |
rs767179634 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:738690 | CGAGACTCCCATCTC[-/A]AAAAAAAAAAAAAAA | 7525 |
rs767204648 | snp | A/T | 1.64827e-05 | 0.00287073 | intron-variant | YES1 | GRCh38.p7 | 18:732975 | TTGCACCTAAAATAA[A/T]GTTGACCATCTTGCT | 7525 |
rs767204778 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:780583 | TGTAAGAAATAAATT[C/T]CTTTTCTTTATAAAT | 7525 |
rs767204790 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:794908 | TGCAACCTTGCCTCC[C/T]GGGTTCAAGCAATTC | 7525 |
rs767232632 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:809297 | ATTATTGTACATTTC[A/G]GAGTATTTGACTTTT | 7525 |
rs767301609 | snp | C/T | 1.72377e-05 | 0.00293573 | missense | YES1 | GRCh38.p7 | 18:746001 | CGTTGATTTCCAGGA[C/T]TCAAAAGTAATCTTT | 7525 |
rs767313581 | in-del | -/GA | | | intron-variant | YES1 | GRCh38.p7 | 18:726222 | CGAGGTCAAGAGATT[-/GA]GACCATCCTGGCCAA | 7525 |
rs767395118 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:811413 | AAACAGCTCTGCCCC[A/G]TGCCCAATAAAGTGA | 7525 |
rs767447200 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:800631 | AAGAAGAAAAGGCTA[A/C]TAAGATGGTGAAGAA | 7525 |
rs767526070 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:768984 | CTGGGATACAGGCAT[A/G]AGCCACTGTGCCTGG | 7525 |
rs767540109 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:782204 | TCATGTGCTTCATTC[C/T]TCTCTCCTGTGGCAC | 7525 |
rs767546809 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:732685 | GTTACCCATCCAATG[A/C]CACAGTAAAGGGAAG | 7525 |
rs767638020 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:789145 | GGCATTCATTGAGTA[C/T]TGATAACAGAACATA | 7525 |
rs767665765 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:764512 | CAGGCGTGAGCCACC[A/G]TGCCTGGCCAAAGTT | 7525 |
rs767704952 | snp | C/T | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:777005 | AACAAAAAGGCCAAT[C/T]AGACATTAACCACAA | 7525 |
rs767706980 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:791856 | GGTCAGGAGTTTGAG[A/T]ACAGCCTGACCAACA | 7525 |
rs767727827 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:790799 | AAACTACCAGAAAAG[C/T]ACAAATATTATGTAT | 7525 |
rs767730645 | snp | A/G | 1.87869e-05 | 0.00306482 | intron-variant | YES1 | GRCh38.p7 | 18:742875 | AATCAAGACTCTTAA[A/G]AACATTATCAACACA | 7525 |
rs767758375 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:778557 | CTAATTGTGACATTA[C/T]ATGCTCTATCTAGTT | 7525 |
rs767764729 | snp | A/T | 0.000118007 | 0.00768047 | intron-variant | YES1 | GRCh38.p7 | 18:751848 | ATTATGTAGCTAACT[A/T]AACAAAACAGAAAAA | 7525 |
rs767771017 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:809592 | AGGTGTGAGCCACCG[C/T]GCCCAGCCTGACGTG | 7525 |
rs767772305 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:728200 | GGTGGATGGCACACA[A/C]CTGTGGTCTCAGCTA | 7525 |
rs767807170 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:772742 | CGGCCAGCATCTCTA[C/T]TTCTGTATTTCTGAT | 7525 |
rs767829767 | in-del | -/AAA | | | intron-variant | YES1 | GRCh38.p7 | 18:803412 | GAATGGGTGGGAAAT[-/AAA]AAAAGCACAGAGAAG | 7525 |
rs767862044 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:773756 | TCACTTAAAATACAA[C/T]CTGATCCAATGCTGA | 7525 |
rs767865322 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:808731 | CTACAACAATGCAAA[A/G]CCACAATATCAACCA | 7525 |
rs767882595 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:799288 | TATGGTATGCAGCCC[C/T]CACTGGGAGGTGGCT | 7525 |
rs767936552 | snp | C/T | 1.66112e-05 | 0.00288189 | synonymous-codon | YES1 | GRCh38.p7 | 18:724427 | AGGCTACTTGAATTA[C/T]AAATTTTCTCCTGGC | 7525 |
rs767940353 | snp | A/C | 1.75742e-05 | 0.00296425 | intron-variant | YES1 | GRCh38.p7 | 18:743454 | TGTAATATCAATTAC[A/C]AAAATTAAGGGGCAT | 7525 |
rs768048101 | snp | A/G | | | missense | YES1 | GRCh38.p7 | 18:736873 | TCTGCTATTTTGCAC[A/G]CAAGATTTTCTCCTA | 7525 |
rs768062320 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:800553 | TAGAAAACAATGTTC[A/C]AGCTTATTAGGGAGG | 7525 |
rs768064071 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:750876 | TATGTGTGAAAGCAT[C/G]AGAGTATAAGAAACT | 7525 |
rs768108098 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:748155 | TCATTGGATGAAGAA[C/T]TAAACTCAAAGAATG | 7525 |
rs768157400 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:766118 | AAGAACTGTGATTTT[C/G]TTGATCCTTCTTACG | 7525 |
rs768161559 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:749958 | TTTATAACACATAAG[A/C]CGTCATTTTTTCAAA | 7525 |
rs768186221 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:735247 | AGATATGGAGCCAAT[C/G]TAAATGACCATTGAC | 7525 |
rs768216394 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:809171 | CATACAAGCCGAAGC[A/G]GATTTTAATTTTGTA | 7525 |
rs768270671 | in-del | -/TGGA | | | intron-variant | YES1 | GRCh38.p7 | 18:748144 | TATTTATGCATTCAT[-/TGGA]TGAAGAATTAAACTC | 7525 |
rs768271742 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:807636 | ATTGCCATATATAGC[C/T]GATAACGTATTTGCA | 7525 |
rs768275004 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:797342 | CCCCTAAAAAAACTG[A/G]GAAAATATAGAAAGA | 7525 |
rs768346648 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:751609 | CAGCCCATGCCCTAC[C/T]TCTCTCATCTCTGGA | 7525 |
rs768357440 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:763948 | AACAGGGCGAAAACC[C/T]GTTTCTACAAAAAAT | 7525 |
rs768382737 | snp | A/T | 1.65877e-05 | 0.00287986 | intron-variant | YES1 | GRCh38.p7 | 18:747898 | ATCAAAATAATTAAT[A/T]AAATATGAAGTAGTG | 7525 |
rs768391233 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:777652 | TTTCTACTAAAAATA[C/G]AAAAATCAGCCAGGC | 7525 |
rs768402137 | snp | A/C/G | 0.000197723 | 0.00994123 | missense | YES1 | GRCh38.p7 | 18:756568 | TCACCTGTTAAACCA[A/C/G]CAGGATATGAACTTG | 7525 |
rs768434163 | snp | C/G | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812833 | GTTTGCTTCTCAGCG[C/G]TACGCTTCCGCACCC | 7525 |
rs768453126 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:798701 | CCCTCCCTCCACCAG[C/T]GCGCTTCCTAACCTT | 7525 |
rs768486923 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:728063 | TTTATGAGCCAGGCA[C/T]GGTGGCTCGCACCTG | 7525 |
rs768504438 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:785800 | AAAAAAAAGCCAGGC[A/G]CTGTTGAGCACCAGT | 7525 |
rs768512920 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:772092 | GGAGTGCAATGCCAC[A/G]ATCTCGGCTCACGGC | 7525 |
rs768558235 | in-del | -/T | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775978 | ATGAATTGTTTCCAG[-/T]TTTTTTTGCTATTAG | 7525 |
rs768559432 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:783147 | CCCAGCTACTCAGGA[A/G]GCCAAGGCAGAGGAT | 7525 |
rs768596468 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:727592 | CTGTTGGCTTTTTGT[C/T]TTCTCTTGTTATTTT | 7525 |
rs768613989 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:784788 | ATTGTTACTCTATTA[C/T]GCCTACCTGGATAAG | 7525 |
rs768624553 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon | YES1 | GRCh38.p7 | 18:724562 | TTCATGGAGGGATTC[C/T]GGACAGCCCTGAGGG | 7525 |
rs768660632 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:768680 | TACCATACCTTTTCT[A/G]TGTTTAGATATGTTA | 7525 |
rs768672415 | in-del | -/TA | | | intron-variant | YES1 | GRCh38.p7 | 18:724814 | TAGAAAATGCTAATC[-/TA]TGTTTTAACATGTCT | 7525 |
rs768703950 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:748856 | ATTAACAATGAGCAA[C/T]AAAGTTAAAAACTGA | 7525 |
rs768729901 | snp | G/T | 3.29766e-05 | 0.00406045 | missense | YES1 | GRCh38.p7 | 18:745777 | TATAGTATCCACCAT[G/T]GTCAAGTTTCCTAAT | 7525 |
rs768743691 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:771530 | TAAACCACTCCGTGG[C/T]ATTTTTCTTTTACAT | 7525 |
rs768900153 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:794629 | GGATGTCCAAAATTC[A/T]AGTGTCAGCAGGGCT | 7525 |
rs768943657 | in-del | -/CTCTCTCT | | | intron-variant | YES1 | GRCh38.p7 | 18:792526 | ACACACTGAGACTCC[-/CTCTCTCT]ATCTCTCTCTCTCTC | 7525 |
rs768965017 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:756268 | TTTAATCTTTATGTT[C/T]CCGGTGCCTACAGTG | 7525 |
rs768990110 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:731795 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 7525 |
rs768990425 | in-del | -/A | 1.66687e-05 | 0.00288688 | intron-variant | YES1 | GRCh38.p7 | 18:756527 | GTGATGTTCTCAAAC[-/A]GACAACATAATTGTC | 7525 |
rs769028947 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:739532 | TGCTAGAGCCCAAGA[A/G]TTCAAGGCTCTTCAA | 7525 |
rs769035840 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:753642 | AGGCGTGCACCTCCA[C/T]GCCCAGCTAATTTTT | 7525 |
rs769045258 | snp | A/G | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722219 | AAATCTCATGTCACA[A/G]GTTGTTGATAAGAGG | 7525 |
rs769071119 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:789744 | ATTTAGGAGCAAACA[A/G]AATTAGGAGAATTTA | 7525 |
rs769087473 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:807856 | GCAATTCTACTCCCC[C/T]CCCCTAAACAACAAT | 7525 |
rs769098533 | in-del | -/G | 8.42716e-05 | 0.00649066 | intron-variant | YES1 | GRCh38.p7 | 18:745864 | AATAAGCACCTGGGT[-/G]AAAAATAAATACTTT | 7525 |
rs769102094 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:741463 | TCAGGTCAGCCACCA[C/T]GCCTGGCCCTCCCTT | 7525 |
rs769143881 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:734928 | TTTGGGAAGCCAAGG[A/C]GTGTGGATCACCTGA | 7525 |
rs769144976 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:769335 | CTAGTACTTTTATAG[A/G]TTCTACAGTATTTTC | 7525 |
rs769158900 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:726276 | TAAAAATACAAAAAA[G/T]TAGCTGGGCGTGGTG | 7525 |
rs769177166 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:782496 | TCAAAATACTTAGGG[C/T]TCACTACTCCATCTA | 7525 |
rs769180619 | in-del | -/AT | | | intron-variant | YES1 | GRCh38.p7 | 18:797867 | TTTCAGAACCTTGAG[-/AT]ATAATTCTTCTAGAC | 7525 |
rs769186500 | snp | C/T | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812979 | GGCAGGGATCCTGTC[C/T]CTGCCCCCAGGAGCT | 7525 |
rs769197198 | in-del | -/C | | | intron-variant | YES1 | GRCh38.p7 | 18:740763 | CTGGAAATAATTGTA[-/C]CCAGTGGTCTGACAA | 7525 |
rs769226626 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:799999 | GTAAGTGGGTGAATA[C/T]GCTTAGGCTAAATAC | 7525 |
rs769250878 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:801015 | GCTGGGTGTGGTGGC[A/G]TGTGCCTGTAATCCC | 7525 |
rs769270563 | in-del | -/ACAG | 1.84242e-05 | 0.00303509 | intron-variant | YES1 | GRCh38.p7 | 18:739817 | AATAAGCTTCCTGTA[-/ACAG]ACAGCAAGATATTCA | 7525 |
rs769305305 | in-del | -/TTGTTA | | | intron-variant | YES1 | GRCh38.p7 | 18:766380 | CCACATCCTTAAGAC[-/TTGTTA]TTAACACTTTTAAAA | 7525 |
rs769306047 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:802123 | AAGTCTAGGGTGGGT[G/T]TAGTGGCTCAAGCCT | 7525 |
rs769356020 | in-del | -/ATTGTATTTACTA | | | intron-variant | YES1 | GRCh38.p7 | 18:743984 | ATATATAGTAAATAT[-/ATTGTATTTACTA]CTTAGTATGTATATA | 7525 |
rs769358180 | in-del | -/CAGTGAAT | | | intron-variant | YES1 | GRCh38.p7 | 18:806637 | AACAGTTCCTTGACA[-/CAGTGAAT]ACTAGGTCAAGAATA | 7525 |
rs769423830 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:760603 | GGGATTTTGGTATCC[A/G]CAGGAGGTTCTAGAA | 7525 |
rs769457712 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:798759 | GACTTTTCACTCCTT[C/T]AGGGGGTACACTGTC | 7525 |
rs769493598 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:731570 | ACTCTCAACATTAGG[-/A]ATACTTCAGTACAAG | 7525 |
rs769552759 | snp | A/C | 1.65798e-05 | 0.00287917 | missense | YES1 | GRCh38.p7 | 18:751798 | GCCACAAATATAGTA[A/C]CACCACCTATCAGAG | 7525 |
rs769562477 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:732435 | AGCAAGACTGTGTTT[-/A]AAAAAAAAAAAAAAA | 7525 |
rs769569984 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:764975 | TCCTGACCTTGTGAT[A/C]CGTCCGCCTTAGCCT | 7525 |
rs769623387 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:767160 | AGTCTTACATTCAAA[A/C]AAAATTTTTTTTGAG | 7525 |
rs769639923 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:762234 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG | 7525 |
rs769657443 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:773107 | CTTGCTTTAATAGCT[A/G]GTAGAAATACACATT | 7525 |
rs769667303 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:752556 | TAATGAATGAACAAT[C/T]GCATCTAATCATTAC | 7525 |
rs769675468 | snp | C/G | 0.000338726 | 0.0130095 | missense | YES1 | GRCh38.p7 | 18:739739 | TATACAGATACCTGA[C/G]CAGCCATATCAACCA | 7525 |
rs769677478 | snp | C/T | 1.65625e-05 | 0.00287766 | intron-variant | YES1 | GRCh38.p7 | 18:756541 | CAGACAACATAATTG[C/T]CCATTTAAATCTCAC | 7525 |
rs769717258 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:771240 | GGCATGGTGGTGCAT[C/G]CCTGTAATCCCAGCT | 7525 |
rs769720309 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:745523 | TCTATTAGCACATTA[C/T]CTGAGTAGCACAATG | 7525 |
rs769753559 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:772503 | AATGGTGCGATCTCG[G/T]CTCACTGCAACCTCC | 7525 |
rs769766379 | snp | A/G | 1.64906e-05 | 0.00287142 | synonymous-codon | YES1 | GRCh38.p7 | 18:743276 | CATCCACACTTCGCC[A/G]AAACATCCTTGTCCT | 7525 |
rs769803923 | in-del | -/TG | | | intron-variant | YES1 | GRCh38.p7 | 18:786072 | CCCAGCCTCCAGAAC[-/TG]TGAGAAGTAAATTTC | 7525 |
rs769819928 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:755601 | AAGAGACAAATGTAT[A/G]GTCAGTCTATGCTTG | 7525 |
rs769829943 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:802405 | AAAAATTAGCCAGGC[A/G]AGGTGGTGCACGCTT | 7525 |
rs769889424 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:802182 | TGTGCCGAGGAGTTC[A/G]AGGCTGTAATGAGCT | 7525 |
rs769950813 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:784437 | GCTGAGAATGAACTC[A/T]GAATATTTCAGCTCA | 7525 |
rs769952577 | in-del | -/AAAG | | | intron-variant | YES1 | GRCh38.p7 | 18:757908 | AACAAAATAGAAAAA[-/AAAG]AGAAAAACCTACCTC | 7525 |
rs769980162 | snp | G/T | 1.8392e-05 | 0.00303243 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724389 | AAGTTCTTTATATTT[G/T]GGCAGATTTGTGCAT | 7525 |
rs770007747 | snp | A/T | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813265 | GCCTTGTAAAGCCAG[A/T]CGTTGAAGAAGGGGG | 7525 |
rs770042876 | snp | A/C/T | 3.3971e-05 | 0.00412123 | synonymous-codon | YES1 | GRCh38.p7 | 18:736944 | CATTCTTTCAATATA[A/C/T]GCCATACCATCAGCA | 7525 |
rs770095038 | in-del | -/AGTC | 1.96759e-05 | 0.00313649 | intron-variant | YES1 | GRCh38.p7 | 18:756862 | ATAAAATATTTTGAG[-/AGTC]AGTTAACACACAGGA | 7525 |
rs770112450 | in-del | -/TAAGAA | | | intron-variant | YES1 | GRCh38.p7 | 18:768379 | GGAGAAATGATATTT[-/TAAGAA]TACTGACTTCCGCTT | 7525 |
rs770130473 | in-del | -/TT | | | intron-variant | YES1 | GRCh38.p7 | 18:730345 | AGGACCCAAGAGGAT[-/TT]TTTTTTTTTTTTTTT | 7525 |
rs770153511 | snp | A/G | 1.64732e-05 | 0.0028699 | missense | YES1 | GRCh38.p7 | 18:756764 | TACTGACAGGCTCTG[A/G]AGTATTTTCAGGTCT | 7525 |
rs770160203 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:728193 | TTAGCTAGGTGGATG[A/G]CACACACCTGTGGTC | 7525 |
rs770207233 | snp | A/C | 1.7235e-05 | 0.00293551 | intron-variant | YES1 | GRCh38.p7 | 18:736771 | GTTAAGCAAAACACA[A/C]AACACATTACAAGCT | 7525 |
rs770207867 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:733625 | CGTCTCTACCAAAAA[A/T]ACAAAAAATTAGCTG | 7525 |
rs770212667 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:808452 | ACACGAACTACCAAT[A/G]AGACAAGACACTTTA | 7525 |
rs770228210 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:777951 | TAACACATTATTATG[C/T]TGTACACACACATTA | 7525 |
rs770287402 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:757327 | GCTAACACGGTGAAA[C/T]CCCGCCTCTACTAAA | 7525 |
rs770331390 | snp | A/C | 0.000152909 | 0.00874249 | splice-donor-variant | YES1 | GRCh38.p7 | 18:739733 | TGTATATATACAGAT[A/C]CCTGAGCAGCCATAT | 7525 |
rs770347963 | snp | C/T | 3.30748e-05 | 0.00406649 | synonymous-codon | YES1 | GRCh38.p7 | 18:751779 | AGCTTCATAATCATA[C/T]AAGGCCACAAATATA | 7525 |
rs770362942 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:791153 | TTCTCGGGAGGCTGA[A/G]GCAGGAGAATCGCTT | 7525 |
rs770371644 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:788660 | GCAGTGGCTCACGCC[G/T]GTAATCCCCGGCACT | 7525 |
rs770373895 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:773641 | ACCTCTAGACTTTCA[C/T]AATCCTGTCCATTGT | 7525 |
rs770444209 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:737271 | CAGCCTGGCCAACAC[A/G]GTGAAACCCTGTCTC | 7525 |
rs770452972 | snp | C/T | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776465 | CTTTACATATGTTTA[C/T]CGGACATTATCTTTT | 7525 |
rs770453772 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:751843 | GGTAAATTATGTAGC[-/T]AACTTAACAAAACAG | 7525 |
rs770457987 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:812014 | CCGCGGGGGCGGGGA[A/C]CCGCGGCGGCGGCGG | 7525 |
rs770468513 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:800158 | CAAAGAGTCTTGAGT[A/G]AAAAACATTTGTGGT | 7525 |
rs770525919 | snp | A/T | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722509 | AGGCTTAATTTAAAG[A/T]GTGACTATATGAGAG | 7525 |
rs770602683 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:787436 | TTTGTTGGGCTGGGC[A/G]CGGTGGCTCACACCT | 7525 |
rs770688407 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:771845 | GGAAGAAAAAATGTT[-/A]AAAAGTATTTCCTTA | 7525 |
rs770765864 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:752891 | GAGGTTGCCATGAGC[C/T]GAGATTATGCCACTG | 7525 |
rs770784175 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:795834 | TAGATGACGGGTTGA[C/T]AGGTGAAGCAAAACA | 7525 |
rs770792682 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:796578 | CTCAAGACCAGCCTG[C/T]CCAACATAGTGAAAC | 7525 |
rs770841486 | snp | A/T | 6.59065e-05 | 0.00574012 | missense | YES1 | GRCh38.p7 | 18:724514 | AAATGTTGGTCTTTC[A/T]TCAGGGTCCTTCTTC | 7525 |
rs770842470 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:725998 | AGTGAGGGCTTACTA[C/T]AATTGAACTTCTTTT | 7525 |
rs770850518 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:791765 | ATATTAAAATCTGGT[A/G]TGTACTGCACCAGGC | 7525 |
rs770857147 | snp | C/T | 4.94328e-05 | 0.00497131 | intron-variant | YES1 | GRCh38.p7 | 18:748056 | CACCGCAAGGTAGAC[C/T]ATTGCCCAAGGTACA | 7525 |
rs770862135 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:732635 | CACCCTGTCAAGGAT[A/C]GTGGCTTTCACTGAC | 7525 |
rs770900153 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:760927 | CACTCTTAATACAGA[A/C]AACTCTTATGCATGA | 7525 |
rs770937983 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:804322 | TTTATTACGAAAAAA[C/T]CTGGGCTAGGCACAG | 7525 |
rs770958330 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:741566 | CCCAGCACTTTGGGA[C/G]GCCAAGGCAGGCTGA | 7525 |
rs770970314 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:806350 | ATGACCTTTAAATTC[A/G]TATTTGAAGGACTGC | 7525 |
rs771001487 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:779512 | AGATTTTTAAAAAAT[G/T]TATTAAATTCAACAC | 7525 |
rs771015036 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:794845 | TTTTTGAGACGGAGT[C/T]TCACTCTGTCGCCCA | 7525 |
rs771024922 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | YES1 | GRCh38.p7 | 18:756736 | GGTTCTGCTCCATAA[C/T]GGCTCACACTTGTAC | 7525 |
rs771025131 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:730343 | AAGGACCCAAGAGGA[-/T]TTTTTTTTTTTTTTT | 7525 |
rs771109224 | snp | A/G | 3.33e-05 | 0.00408031 | missense | YES1 | GRCh38.p7 | 18:743052 | GGCATCATTGTACCT[A/G]GTTTTAGTGTTTTGA | 7525 |
rs771118002 | snp | C/T | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:814229 | AAGTTTTCAATCTTA[C/T]ATTTAGTGGCTCACT | 7525 |
rs771153600 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:802836 | ACCTATAATCCTAGC[A/G]CTTCGGGAGGTTGAG | 7525 |
rs771166809 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:803646 | AATAGCAATGCCTTA[C/T]TGGGAGAATCTGAGT | 7525 |
rs771185667 | snp | A/G | 1.66927e-05 | 0.00288895 | intron-variant | YES1 | GRCh38.p7 | 18:747869 | AGTAGAATGTGCATT[A/G]AAACATTTCAAAAAT | 7525 |
rs771193015 | in-del | -/AT | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723838 | GTGGTCTAACATTTA[-/AT]CAAGTTTGAGATCCT | 7525 |
rs771255145 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:731406 | GGTATCAGTGAATAA[C/T]AGCAACCAGACAAAG | 7525 |
rs771257492 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:810301 | ATCAATACATACCAT[A/G]AAGAAATTTTACTTG | 7525 |
rs771329396 | snp | C/T | 1.8051e-05 | 0.0030042 | missense | YES1 | GRCh38.p7 | 18:745954 | TATTCATACCTTTAG[C/T]TGTTTCACTCTCTCT | 7525 |
rs771329842 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:772003 | CAGAAATTACAAGAC[A/C]GTCTGATCGTACACC | 7525 |
rs771333137 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:778252 | TTTCTACTACCCATA[C/T]GATCTTCAGGGAAGC | 7525 |
rs771374741 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:767166 | ACATTCAAAAAAAAT[G/T]TTTTTTGAGACAAGG | 7525 |
rs771394702 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:799106 | ACCAATACTGTAACC[C/T]GAATTAAGATACCAT | 7525 |
rs771402516 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:760303 | GGTGAAACCCTGCCT[C/G]TACTAAAAATACAAA | 7525 |
rs771458469 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:792734 | GGAAGGCTGAGAAGG[A/G]AGGATTGCTTGAGGC | 7525 |
rs771487857 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:729721 | AACCTCCACCTCCTG[G/T]GTTCAAGCGATTCTC | 7525 |
rs771513356 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:779714 | CAAGAATCTTTATTC[G/T]CTCAGATTTTCACAC | 7525 |
rs771662805 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:724690 | TACCACTAGGAAAAC[A/G]TAACAAACCCCCTAG | 7525 |
rs771664163 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:774978 | CATACTCCCAGCTTA[C/T]TGTATGTATGGCAGA | 7525 |
rs771668758 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:807270 | ACCTGGGAGGCAGAG[C/G]TTGCAGTGAGCCAAG | 7525 |
rs771681048 | snp | C/T | 1.64866e-05 | 0.00287106 | synonymous-codon | YES1 | GRCh38.p7 | 18:747928 | GCCATACTCTTCTGC[C/T]TGAATGGAATCTGCA | 7525 |
rs771685902 | snp | A/G | 1.69596e-05 | 0.00291196 | intron-variant | YES1 | GRCh38.p7 | 18:736794 | TACAAGCTTTTATGT[A/G]AAAGTAATTTTACCT | 7525 |
rs771689550 | in-del | -/AA | | | intron-variant | YES1 | GRCh38.p7 | 18:754713 | AGAGACTCCAACTCC[-/AA]AAAAAAAAAAAAAAA | 7525 |
rs771727327 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:733939 | AGATATTTAGACAAA[C/T]AGATGATCAATTTTC | 7525 |
rs771772473 | snp | A/G | 1.65416e-05 | 0.00287586 | synonymous-codon | YES1 | GRCh38.p7 | 18:743027 | CTGAGCTTCTTGAAG[A/G]AAAGCTTCTGGCATC | 7525 |
rs771785139 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:789607 | ACAAAAACCCCCAAA[A/C]CAAAAAAACCCAACA | 7525 |
rs771791902 | snp | A/G | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723523 | CATCCCCATAAGGAC[A/G]TATAAGCAATACTCA | 7525 |
rs771802200 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:747757 | TCTAAGTGAATAGTA[C/T]GACATTAGTTATTAA | 7525 |
rs771823744 | in-del | -/TG | | | intron-variant | YES1 | GRCh38.p7 | 18:733888 | TTTAAGTTATTTATA[-/TG]TGTTTGTAGATAGTG | 7525 |
rs771870538 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:808172 | CCATCAAGTCTGCTA[A/G]TTCCAAGACAACAGT | 7525 |
rs771891606 | snp | A/T | 1.65573e-05 | 0.00287721 | intron-variant | YES1 | GRCh38.p7 | 18:743244 | ATGACAGAAAACAAA[A/T]ATTCAGGCTTCTTAC | 7525 |
rs771910366 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:739138 | CCTGGAAACATCTAT[G/T]TTCTAAGAAACCGTA | 7525 |
rs771916800 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:726353 | TCGCTTGAACCTGGG[A/C]GGTGGAGGTTGCAGT | 7525 |
rs771983371 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:737732 | TACATTTTGATTGAT[-/A]TGACTGAGACGGGGT | 7525 |
rs771992652 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:763580 | TGGTGGCACATCCCT[A/G]TAGTTCTAGCTACTT | 7525 |
rs771998646 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:746556 | TCACAGAAAATGAGA[A/C]GAAAGACAAAAGGAC | 7525 |
rs772020145 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:799447 | GGGCATGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 7525 |
rs772052670 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:755367 | ACTACTCGTGCCTCA[C/G]CCTCCCGAGTAGCTG | 7525 |
rs772068535 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:794510 | ATATATGAACTACTG[C/T]ATTACTTTCCTTGCC | 7525 |
rs772089867 | snp | A/T | 1.64751e-05 | 0.00287007 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724377 | GAAAATCTACACAAG[A/T]TCTTTATATTTTGGC | 7525 |
rs772116754 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:796135 | CATGAAAAAGTAAAT[A/G]CATATGAATAGCTGA | 7525 |
rs772146315 | in-del | -/TTC | | | intron-variant | YES1 | GRCh38.p7 | 18:729456 | ACAATTTCCATTTGA[-/TTC]TTTTTTTTTTAATAG | 7525 |
rs772151168 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:729872 | CCTTGTGATCCACCC[A/G]CCTTGGCTTCCCAAT | 7525 |
rs772156124 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, intron-variant | YES1 | GRCh38.p7 | 18:732888 | GCAGAATTCCAAATG[A/G]CCAGACATCAGACTT | 7525 |
rs772171956 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:783473 | AATGCAATGTTATAA[C/T]AAAATTGAATCTGAA | 7525 |
rs772240752 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:782068 | CACTTCCCTTGCTTC[C/T]CCATTTTCTCTCCTC | 7525 |
rs772308392 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:779890 | CATCCACTTGTTTCT[A/G]TAACAATGTATGTAG | 7525 |
rs772315704 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:792951 | TTCCATGATATTATA[C/T]ATCTATAAAGTTCAA | 7525 |
rs772342447 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:752708 | AGCACTTTGGGAGGC[C/T]GAGGTGGGCAAATCA | 7525 |
rs772368524 | snp | G/T | 1.64727e-05 | 0.00286986 | missense | YES1 | GRCh38.p7 | 18:756646 | GAGGATCCTCCAAAT[G/T]GTGTCATGGAAAGAC | 7525 |
rs772387453 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:743762 | AATACAAAAGTTAGC[C/T]GGGCATGGTGGTGCA | 7525 |
rs772407330 | snp | C/T | 1.65015e-05 | 0.00287237 | missense | YES1 | GRCh38.p7 | 18:745810 | TGTAGTGTTTCACAT[C/T]GTCACCCCTTATCTC | 7525 |
rs772418350 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:759340 | GGCGAGGTGGCGGGC[A/G]CCTGTAATTCCAGCT | 7525 |
rs772418945 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:787665 | CAGTGAGCTGAAATC[A/G]CGCCACTGCACTTCA | 7525 |
rs772444326 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:767321 | CGCCTGGCTCATTTT[C/T]GTATTTTTTTGTAAG | 7525 |
rs772469496 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:760473 | AGATTCTGTCTAAAA[A/C]AAACAAACAAACAAC | 7525 |
rs772523762 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:738816 | TACATATAGACTTTA[C/T]ATTTGTGGAAACATC | 7525 |
rs772525934 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:735796 | ACTGAAATCACCACT[A/G]AAGAACTAGTTTCCC | 7525 |
rs772531363 | snp | C/T | 6.68338e-05 | 0.00578035 | intron-variant | YES1 | GRCh38.p7 | 18:724668 | ATTAAAGAACAATGG[C/T]CCTAACTACCACTAG | 7525 |
rs772551826 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:781062 | CACCTGAGGTCAGGA[A/G]TTTGAAACCAGCCTG | 7525 |
rs772569320 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:737439 | GCCTGGGAAACAGAG[A/C]GAGACTCAGCCTCAA | 7525 |
rs772604774 | in-del | -/AT | 1.78014e-05 | 0.00298335 | intron-variant | YES1 | GRCh38.p7 | 18:743138 | TTTATATTTTAAAGG[-/AT]TTTAGACCAAACTTC | 7525 |
rs772672122 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:768282 | ATCTCTACAAATTTT[A/T]ATCATACAAATTTTA | 7525 |
rs772706423 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:732148 | GTACATATTTAAAAA[A/T]ATATACCATGATGGG | 7525 |
rs772758859 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:751409 | AGCATCAAACTCTCT[C/T]TATAAAGTTTTTTAA | 7525 |
rs772793059 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:798921 | CAAAGGTTCTTTCTA[C/G]AATTTACATATCACT | 7525 |
rs772807700 | in-del | -/CTT | | | intron-variant | YES1 | GRCh38.p7 | 18:727525 | GTTTCTCCTCTCTTG[-/CTT]TTTAATTTGATTAAA | 7525 |
rs772821107 | snp | C/T | 8.23866e-05 | 0.00641767 | intron-variant | YES1 | GRCh38.p7 | 18:748051 | GCAATCACCGCAAGG[C/T]AGACTATTGCCCAAG | 7525 |
rs772827942 | snp | C/T | 4.96422e-05 | 0.00498183 | missense | YES1 | GRCh38.p7 | 18:756800 | TAATGGCTGGACTTT[C/T]GTTTTCTTTACTTTT | 7525 |
rs772886494 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:750578 | TGATTCTGTCCCAGG[C/T]TGAGAACCATTGGTC | 7525 |
rs772890030 | snp | C/T | 1.66582e-05 | 0.00288597 | synonymous-codon | YES1 | GRCh38.p7 | 18:736812 | AGTAATTTTACCTTG[C/T]CTTGCTGTGTATTCA | 7525 |
rs772903998 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:741966 | ACTTTTGGTTTCAGT[C/T]CCCTTTTGAGGGGAA | 7525 |
rs773011806 | snp | G/T | 1.64814e-05 | 0.00287061 | missense | YES1 | GRCh38.p7 | 18:747933 | ACTCTTCTGCCTGAA[G/T]GGAATCTGCAGGCGC | 7525 |
rs773025552 | snp | C/G | 1.73003e-05 | 0.00294106 | missense | YES1 | GRCh38.p7 | 18:736955 | TATATGCCATACCAT[C/G]AGCAATCTTGGAAAG | 7525 |
rs773043073 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:793201 | CATGCCACCATGCCC[A/G]GATGATTTTTTGTAT | 7525 |
rs773056717 | snp | C/T | 1.84869e-05 | 0.00304024 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724382 | TCTACACAAGTTCTT[C/T]ATATTTTGGCAGATT | 7525 |
rs773092916 | in-del | -/TG | | | intron-variant | YES1 | GRCh38.p7 | 18:792566 | CTCTCCCTCTGTATA[-/TG]TGTGTGTGTGTGTGT | 7525 |
rs773095961 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:766415 | AACTGCTAATTAAAT[A/G]TAAGTTAAAACCGCA | 7525 |
rs773099985 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:780407 | ACAACTGGTGGCTTT[A/G]TAAGAGGAAGAGAGA | 7525 |
rs773138033 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:806143 | TATATGAACAAGTCA[C/T]AATTGTAATACTGAT | 7525 |
rs773141032 | in-del | -/C | | | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721560 | AACAAAACAAAACAA[-/C]AAAAAAAAGAAAATT | 7525 |
rs773163621 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:773346 | CATCTTCCTGGATAA[C/T]GGGCAAGAGAAGGCA | 7525 |
rs773203469 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:745531 | CACATTATCTGAGTA[C/G]CACAATGCAAGTACT | 7525 |
rs773225560 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:772964 | TAACTGCACTAACCT[A/G]CTGACCAGTTATGGT | 7525 |
rs773228062 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:805038 | TTTTTATAATCTTTA[C/T]TTATATCTAATGTGA | 7525 |
rs773292050 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:733639 | ATACAAAAAATTAGC[C/T]GGGCGAGGTGGCAGG | 7525 |
rs773323129 | snp | C/T | 3.74567e-05 | 0.00432746 | intron-variant | YES1 | GRCh38.p7 | 18:742884 | TCTTAAAAACATTAT[C/T]AACACAAATACCTAA | 7525 |
rs773344434 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:740695 | AATGAGGAATTAAAG[A/G]GTTTTAAAAATAGAA | 7525 |
rs773348637 | snp | C/T | 1.80615e-05 | 0.00300506 | splice-acceptor-variant | YES1 | GRCh38.p7 | 18:756837 | GCCCATTATCAAATC[C/T]ACAGAGACAATAAAA | 7525 |
rs773366673 | snp | C/T | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813355 | CTGAACCTTGAGGCC[C/T]TTCTGCTGCAGTCAC | 7525 |
rs773387962 | snp | A/C | 1.64762e-05 | 0.00287016 | missense | YES1 | GRCh38.p7 | 18:756579 | ACCAGCAGGATATGA[A/C]CTTGGCACCACTGAA | 7525 |
rs773434019 | in-del | -/AAAAAAAAAAAAAA | | | intron-variant | YES1 | GRCh38.p7 | 18:733789 | ACTCCGTCTCAAAAA[-/AAAAAAAAAAAAAA]AAAAAAAAAGCATGG | 7525 |
rs773438579 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:755614 | ATAGTCAGTCTATGC[C/T]TGTAGTGGGGATTTA | 7525 |
rs773492700 | snp | A/G | 1.65329e-05 | 0.0028751 | missense | YES1 | GRCh38.p7 | 18:745831 | CCCTTATCTCATCCC[A/G]ATCACGAATAGAAAG | 7525 |
rs773507709 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:729472 | TCTTTTTTTTTTAAT[A/C]GATTCCAATTCTGCT | 7525 |
rs773565802 | snp | C/T | 1.65647e-05 | 0.00287786 | synonymous-codon | YES1 | GRCh38.p7 | 18:743036 | TTGAAGGAAAGCTTC[C/T]GGCATCATTGTACCT | 7525 |
rs773597653 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:797972 | TTCACACTATGATCT[A/C]TTAGGACAAAAAATG | 7525 |
rs773622143 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:797094 | TGCACAGACATGGAA[A/G]AGTCTTTGCAACATA | 7525 |
rs773623267 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:728196 | GCTAGGTGGATGGCA[C/T]ACACCTGTGGTCTCA | 7525 |
rs773685636 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:741320 | ACAATCACAGCTCAC[C/T]ATGGCCTTAACCTCC | 7525 |
rs773732886 | snp | A/G | 3.37587e-05 | 0.00410831 | intron-variant | YES1 | GRCh38.p7 | 18:724679 | ATGGTCCTAACTACC[A/G]CTAGGAAAACATAAC | 7525 |
rs773759576 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:734143 | ACTTAGCCAGGTGTG[C/G]TGGTGCATGCCTGTA | 7525 |
rs773770683 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:757570 | TCACACCTGTAATTG[G/T]AGCACTTTGGGATGC | 7525 |
rs773774276 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:765025 | AGGCGTGAGCCACCT[C/G]GCCCGGCTTATCTGA | 7525 |
rs773778158 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:800560 | CAATGTTCCAGCTTA[C/T]TAGGGAGGACAAAGG | 7525 |
rs773804660 | snp | A/C | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776501 | AGGTCTGTTCAAGAC[A/C]CTTATCCATTGTTCT | 7525 |
rs773862269 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:778064 | TTGTTATTATTATTT[A/T]ATTTGATCCCAAAAT | 7525 |
rs773890031 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:749803 | GGGCAGAGCTTGCAG[A/T]GAGCCGAGATTGCGC | 7525 |
rs773912419 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:760995 | AAGAGACAATTCACA[A/G]CACAGGAAAGGCCAA | 7525 |
rs774007197 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:787641 | CTTTAACCTGGGATG[C/T]GGAGGTTGCAGTGAG | 7525 |
rs774045264 | snp | A/G | 1.7263e-05 | 0.00293789 | stop-gained | YES1 | GRCh38.p7 | 18:745987 | CTAAGAAAATACCTC[A/G]TTGATTTCCAGGATT | 7525 |
rs774064658 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:783266 | ATTTTAGCTACAGAC[C/G]CAAAGAGAAAGTTGA | 7525 |
rs774125157 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:753085 | TTGCAAACAAAACAA[A/G]TAATAAAACAGATGT | 7525 |
rs774137318 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:746375 | CAAATGGAAATATTA[A/T]GACTATGACAGGAAG | 7525 |
rs774143672 | snp | A/G | 6.84885e-05 | 0.00585146 | intron-variant | YES1 | GRCh38.p7 | 18:736783 | ACACAACACATTACA[A/G]GCTTTTATGTAAAAG | 7525 |
rs774160138 | snp | C/T | 1.65616e-05 | 0.00287759 | intron-variant | YES1 | GRCh38.p7 | 18:747902 | AAATAATTAATAAAA[C/T]ATGAAGTAGTGCCAT | 7525 |
rs774165438 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:811826 | CCCCAAAGACAAGGG[A/G]TGGGGAGTGTCCCCA | 7525 |
rs774168125 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, intron-variant | YES1 | GRCh38.p7 | 18:732941 | GCAGCTTCAGGAGCT[A/G]TCCATTTGATTGGAA | 7525 |
rs774176532 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:737317 | CATTAGCTGGGTGTG[A/G]TGGCACATACCTGTA | 7525 |
rs774193234 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:781853 | TAGCACATACCCGAA[A/T]GACAGCAGTGTTTGC | 7525 |
rs774219905 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:725350 | AGGCCATCCCTTGTA[-/T]CTCTTGGAAACTTTA | 7525 |
rs774254056 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:768870 | ACCACGCCTGGCTAA[C/T]TTTTGTATTTTTAGT | 7525 |
rs774283273 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:795968 | TATGAGTAAGTAAAA[C/T]AAAAGTTCAGAGTCT | 7525 |
rs774330229 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:744442 | TCGCCCAGGATGGAG[-/T]GCAGTGGTGTGGTCT | 7525 |
rs774362942 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:807227 | CAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 7525 |
rs774366482 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:746596 | AGTAAGAAGCACCAT[A/G]GTAGAACAAAGAGTT | 7525 |
rs774374829 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:794855 | GGAGTCTCACTCTGT[C/T]GCCCAGGCTGGAGAG | 7525 |
rs774385509 | in-del | -/TTTTTTTTTTT | | | intron-variant | YES1 | GRCh38.p7 | 18:787081 | GTGATACATACTGTC[-/TTTTTTTTTTT]TTTTTTTTTTTTTTT | 7525 |
rs774426890 | snp | A/G | | | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721300 | CCCAGCACTTTGGGA[A/G]GCCGAAGCGGACGGA | 7525 |
rs774442213 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:779731 | TCAGATTTTCACACC[C/T]TACTTCCAGTCTTTT | 7525 |
rs774449335 | snp | C/G | 1.67354e-05 | 0.00289265 | intron-variant | YES1 | GRCh38.p7 | 18:751841 | AAGGTAAATTATGTA[C/G]CTAACTTAACAAAAC | 7525 |
rs774457450 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:741685 | GCATGCACCTGTAAT[C/T]CCAGCTACTCAGGAG | 7525 |
rs774470075 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:754714 | GAGACTCCAACTCCA[-/A]AAAAAAAAAAAAAAA | 7525 |
rs774500026 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:790104 | TTCCCGGCTGAGTGC[A/C]GTGGCTCATGCCTGT | 7525 |
rs774565886 | snp | C/T | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776825 | AAAGTAGAACTCTGT[C/T]TGTAACACTCCCTTG | 7525 |
rs774644140 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:802931 | TATTCTAAAAAAAAA[-/T]AAAAATAAAAAACAG | 7525 |
rs774683454 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:779763 | TCAAGATTTTTGACC[A/T]GCAAATTACAGTAAA | 7525 |
rs774754470 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:800493 | GAGTTGTACTGTAGA[C/T]ATTGTGGGATAATAA | 7525 |
rs774849451 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:810336 | GACATTAATTTTTCA[C/G]CTTGTGAATTTCCTG | 7525 |
rs774905926 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:796251 | GTTAGGTTACAGTCC[C/T]AGCGTGTAATTTGAG | 7525 |
rs774917864 | snp | A/C | 1.64762e-05 | 0.00287016 | synonymous-codon | YES1 | GRCh38.p7 | 18:724574 | TTCTGGACAGCCCTG[A/C]GGGCACGGCATCCTG | 7525 |
rs774922659 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:751509 | AACCACAGCAGCACA[A/C]ATTGTAGAAGTAATA | 7525 |
rs774962049 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:779403 | GTGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 7525 |
rs774977871 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:809244 | TAAAGAAAACGAACT[-/A]GAACTTTATTTAGAA | 7525 |
rs774998072 | snp | G/T | 1.80094e-05 | 0.00300073 | missense | YES1 | GRCh38.p7 | 18:745956 | TTCATACCTTTAGTT[G/T]TTTCACTCTCTCTTA | 7525 |
rs775132002 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:787958 | CAACAACTGCTTTAG[C/T]CTCGAAATGTCCAGG | 7525 |
rs775148751 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:806509 | TTTGTTTTGTTTGCG[A/C]AAAGTCCATAGCTGT | 7525 |
rs775169510 | snp | G/T | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:814253 | GCTCACTTGTTTCCA[G/T]GAATATTTTTTAAAA | 7525 |
rs775317739 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:726182 | TGTAATCCCAGCACT[C/T]TGGGAGGCCGAGGCA | 7525 |
rs775336943 | snp | A/T | 2.08557e-05 | 0.00322915 | intron-variant | YES1 | GRCh38.p7 | 18:739849 | CATAAAAAATAAGCA[A/T]ATCTTATATTAGGAT | 7525 |
rs775375757 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:748066 | TAGACTATTGCCCAA[A/G]GTACAATATATTGCA | 7525 |
rs775428573 | snp | A/G | 1.68499e-05 | 0.00290253 | missense | YES1 | GRCh38.p7 | 18:739745 | GATACCTGAGCAGCC[A/G]TATCAACCAGCTGTG | 7525 |
rs775453732 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:797177 | AGAAAAAGACAAATA[A/G]CCCAATAGTAAAACT | 7525 |
rs775480874 | snp | C/T | 1.65334e-05 | 0.00287514 | missense | YES1 | GRCh38.p7 | 18:743406 | TTGTGGCATAAACCA[C/T]CAGCATGTTCTAGAT | 7525 |
rs775483358 | snp | A/C | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723573 | TAAAAAGGGCTTTTA[A/C]AATGCTGGGTCTTAC | 7525 |
rs775510558 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:729475 | TTTTTTTTTAATAGA[C/T]TCCAATTCTGCTCAA | 7525 |
rs775521015 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:733941 | ATATTTAGACAAACA[C/G]ATGATCAATTTTCCT | 7525 |
rs775541029 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:780313 | GGTGATTGGATCATG[A/C]GGACTCCACCCTTAT | 7525 |
rs775576656 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:731489 | AAGAGGAATATGTTA[G/T]ATAACATGCAAAACC | 7525 |
rs775592331 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:781085 | CCAGCCTGGCCAACA[C/T]GGTGAAACCCCGTTT | 7525 |
rs775596082 | in-del | -/ACACACAC | | | intron-variant | YES1 | GRCh38.p7 | 18:795914 | TCCCAGAACTTAAAC[-/ACACACAC]ACACACACACACACA | 7525 |
rs775600774 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:755475 | CAGGCTGGTCTCAAA[C/T]TCCTGAGCTCAGGCA | 7525 |
rs775603690 | snp | C/T | 1.64749e-05 | 0.00287005 | missense | YES1 | GRCh38.p7 | 18:724551 | AGATTCATCAATTCA[C/T]GGAGGGATTCTGGAC | 7525 |
rs775677634 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:809741 | ACCAAGCACCTTATA[C/T]AGACATTACACACTG | 7525 |
rs775715528 | in-del | -/C | | | intron-variant | YES1 | GRCh38.p7 | 18:802544 | AGTGAAACTCCATCT[-/C]AAAAAAAAAAAAAAA | 7525 |
rs775732572 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:810515 | AGCAAAACCTAACTA[C/T]GAAATTAAAGCCATT | 7525 |
rs775768925 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:773862 | TTTGAGACGGAATCT[C/T]GCTCTGTCGCCCAGG | 7525 |
rs775785424 | in-del | -/C | | | intron-variant | YES1 | GRCh38.p7 | 18:780036 | GTCAGGAGTTCGAAA[-/C]CAGCCTGGCCAACAT | 7525 |
rs775820236 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:768326 | AATGCCTGCTGGGAT[G/T]CTGACTGGGATTATT | 7525 |
rs775903718 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:777192 | GAACAAGAAGGGGAG[A/G]AGGCTAAAACAGCAA | 7525 |
rs775958102 | in-del | -/ACCAAACT | 1.78495e-05 | 0.00298738 | intron-variant | YES1 | GRCh38.p7 | 18:743145 | TTTAAAGGATTTTAG[-/ACCAAACT]TCAGTGAACAGCACT | 7525 |
rs775963265 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:766153 | CCAAGTCCTTCAGGG[A/G]AGGCTCAGTGCCTAT | 7525 |
rs775975076 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:788798 | AGACATGGTGGTGTG[C/T]GCCTGTAGTGCCAGC | 7525 |
rs775977830 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:805431 | CCATCATTGAAACTT[C/T]CTTAGGCAGAGCATG | 7525 |
rs775987569 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:797539 | ATCAGGTCTGACCAC[C/T]CACTAACACAAGAAA | 7525 |
rs775990971 | snp | A/C | 1.64741e-05 | 0.00286998 | synonymous-codon | YES1 | GRCh38.p7 | 18:756774 | CTCTGGAGTATTTTC[A/C]GGTCTGTATTTAATG | 7525 |
rs776042740 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:784922 | GAGAATTCACAGAAC[A/G]TGGACATCTCTGGGG | 7525 |
rs776058735 | snp | C/G | 1.64827e-05 | 0.00287073 | missense | YES1 | GRCh38.p7 | 18:743287 | CGCCGAAACATCCTT[C/G]TCCTAGTTTAACCTC | 7525 |
rs776075563 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:750103 | ACTGTCTAAATTAAA[A/G]TGTTATAAATGCCTA | 7525 |
rs776120321 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:798378 | TATTCATCTTCTGAC[-/A]ACATCCTAAGAGCTT | 7525 |
rs776120861 | in-del | -/AACC | | | intron-variant | YES1 | GRCh38.p7 | 18:796678 | CAGGAGAATCACTTG[-/AACC]CGGGAGGTGGAGGTT | 7525 |
rs776157403 | snp | A/G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:764882 | GGATTACAGGTGCAC[A/G/T]CCACCACACCCGGCT | 7525 |
rs776164809 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:741646 | CCATCTGTAGAAAAA[C/T]ACACAAATTATCTAT | 7525 |
rs776241168 | in-del | -/ACA | | | intron-variant | YES1 | GRCh38.p7 | 18:734599 | GAGCAACTACAACAT[-/ACA]ACATCACTAATCATC | 7525 |
rs776251115 | snp | C/G | 1.6968e-05 | 0.00291268 | splice-donor-variant | YES1 | GRCh38.p7 | 18:739734 | GTATATATACAGATA[C/G]CTGAGCAGCCATATC | 7525 |
rs776317294 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:804770 | AACACAAAAATTAGC[C/G]GGGTGTGGTGGCACA | 7525 |
rs776336590 | snp | C/T | 5.34202e-05 | 0.00516791 | intron-variant | YES1 | GRCh38.p7 | 18:743459 | TATCAATTACAAAAA[C/T]TAAGGGGCATATAGT | 7525 |
rs776424908 | snp | C/G | 1.77735e-05 | 0.00298101 | intron-variant | YES1 | GRCh38.p7 | 18:736966 | CCATCAGCAATCTTG[C/G]AAAGAGAAAAACAAA | 7525 |
rs776553359 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:790127 | ATGCCTGTAATCTCA[C/G]CACTTTGGGAGACCA | 7525 |
rs776558661 | snp | C/T | 1.64768e-05 | 0.00287021 | intron-variant | YES1 | GRCh38.p7 | 18:748059 | CGCAAGGTAGACTAT[C/T]GCCCAAGGTACAATA | 7525 |
rs776569866 | snp | G/T | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:814296 | AGGAAGAGAAAACTG[G/T]AAAGTCTTACTGAGT | 7525 |
rs776578110 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:785820 | TGAGCACCAGTAGTC[C/T]CAGCTACTTGGGAGG | 7525 |
rs776618133 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | YES1 | GRCh38.p7 | 18:756749 | AATGGCTCACACTTG[C/T]ACTGACAGGCTCTGG | 7525 |
rs776622730 | in-del | -/C | | | intron-variant | YES1 | GRCh38.p7 | 18:764119 | AGCGAGACTCCCTCT[-/C]AAAAAAAAAAAAAAA | 7525 |
rs776644846 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:799461 | ACGCCTGTAATCCCA[A/G]CACTCTGGGAGGCCA | 7525 |
rs776660464 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:771571 | AAAACTTTTTTGTGA[G/T]GGGGTTTCACTTTGT | 7525 |
rs776743873 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:811762 | CCCCTACTTCGGCCG[C/T]AGGGGCAAAAATAAA | 7525 |
rs776745532 | snp | G/T | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813075 | ACTATCCCAGTCATG[G/T]TGGCTTTGGCTTATG | 7525 |
rs776746622 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:753737 | GTGATCTACCTGAGT[C/T]GGCCTCCCAAAGTGC | 7525 |
rs776746711 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:769397 | TGTCTTGCTCTTTAC[C/T]CTCCTACATACGTCT | 7525 |
rs776754285 | in-del | -/CA | | | intron-variant | YES1 | GRCh38.p7 | 18:796931 | AAAAAAAAATTACCT[-/CA]CAACATACATAAAAT | 7525 |
rs776791950 | in-del | -/AA | 1.86159e-05 | 0.00305084 | intron-variant | YES1 | GRCh38.p7 | 18:756846 | CAAATCTACAGAGAC[-/AA]TAAAATATTTTGAGA | 7525 |
rs776798016 | in-del | -/T | 1.8703e-05 | 0.00305796 | intron-variant | YES1 | GRCh38.p7 | 18:745931 | TTATACTTATACTAA[-/T]ATAACAATATTCATA | 7525 |
rs776838526 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:770334 | CAATGTGAGTGATCA[A/G]CAAGGACTTTCCCCT | 7525 |
rs776838979 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:768681 | ACCATACCTTTTCTA[C/T]GTTTAGATATGTTAT | 7525 |
rs776905108 | snp | A/C | 1.64732e-05 | 0.0028699 | missense, intron-variant | YES1 | GRCh38.p7 | 18:732927 | ACCGACCATACAGTG[A/C]AGCTTCAGGAGCTGT | 7525 |
rs776927501 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:734512 | AGTGAGCCAAGATCG[C/T]GCCACTGCACTCCAG | 7525 |
rs776943758 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:802288 | AATTAGAAAGTATTG[C/T]CAGGCGTGGTGGCTC | 7525 |
rs776968653 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:731661 | CTCCTTCCCCCTAGA[A/G]ACTATATAAATCTCT | 7525 |
rs776968703 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:746559 | CAGAAAATGAGAAGA[A/C]AGACAAAAGGACAAA | 7525 |
rs777029807 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:739650 | CCCACCATTTCACTA[C/T]ACATACTATAATATT | 7525 |
rs777089485 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:782717 | TTCTGAATTTTACAT[-/A]AGAGTCTCGTTCTGT | 7525 |
rs777112591 | in-del | -/AA | 1.64728e-05 | 0.00286987 | frameshift-variant | YES1 | GRCh38.p7 | 18:756626 | TCCAAAAGGCGTTAC[-/AA]CCCTGAGGATCCTCC | 7525 |
rs777130506 | snp | C/T | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775229 | CACGAATGTTTGCAA[C/T]TGTGATCATTTTGAT | 7525 |
rs777169581 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:737743 | TTGATTGACTGAGAC[A/G]GGGTCTCACTCTGTC | 7525 |
rs777181321 | snp | C/T | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776314 | TTCTCGTGCCTCAGC[C/T]TCCCATGTAGCTGGG | 7525 |
rs777186126 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon | YES1 | GRCh38.p7 | 18:756663 | TGTCATGGAAAGACT[A/G]CTGAAATTAACTGCT | 7525 |
rs777211673 | snp | C/T | 1.64795e-05 | 0.00287045 | missense | YES1 | GRCh38.p7 | 18:724596 | GGCATCCTGTATCCT[C/T]GCTCCACTTGTTCTA | 7525 |
rs777216293 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:789130 | TCCACACTGTTGTTT[A/G]GCATTCATTGAGTAC | 7525 |
rs777225739 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:810046 | CCAAGTTTGGGTGAC[C/T]CCAGCGCTTAGCATC | 7525 |
rs777264688 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:780804 | CGGTCTGGATTATTG[C/T]AAAAGCCTCTTTAAC | 7525 |
rs777315243 | snp | A/C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:800753 | GATGTTCATATAACA[A/C/G]TAATAGTTACAAGGC | 7525 |
rs777323247 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:811445 | AGCTGGAAGCAATTA[C/T]CAAGAAGAAAAACAC | 7525 |
rs777368724 | in-del | -/AG | 1.6617e-05 | 0.00288239 | intron-variant | YES1 | GRCh38.p7 | 18:751810 | GTAACACCACCTATC[-/AG]AGGGAAAAAAGACCA | 7525 |
rs777377090 | snp | A/C | | | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721553 | AAAAAAAAAACAAAA[A/C]AAAACAAAAAAAAAA | 7525 |
rs777380403 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:771413 | GGGTATTATTTCTTA[A/C]ATGAACTTGTGTTTA | 7525 |
rs777395478 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:746163 | CAAAGAATAGCTAGA[G/T]AACATGGCTCAAAAT | 7525 |
rs777396334 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:731286 | AAGAGACCAGGGTAA[C/T]AGAAGAATCATCACC | 7525 |
rs777396959 | in-del | -/GCAAG | 1.75582e-05 | 0.0029629 | intron-variant | YES1 | GRCh38.p7 | 18:743122 | AACACATTTTAGGAA[-/GCAAG]TTTATATTTTAAAGG | 7525 |
rs777421677 | snp | A/T | 1.6691e-05 | 0.00288881 | intron-variant | YES1 | GRCh38.p7 | 18:756516 | TATTACCCAAGGTGA[A/T]GTTCTCAAACAGACA | 7525 |
rs777490475 | in-del | -/TTT | | | intron-variant | YES1 | GRCh38.p7 | 18:794829 | TTTTGTTTTGTTTTG[-/TTT]TTTGAGACGGAGTCT | 7525 |
rs777502618 | snp | A/C | 3.41769e-05 | 0.00413368 | intron-variant | YES1 | GRCh38.p7 | 18:739723 | AATGGATACATGTAT[A/C]TATACAGATACCTGA | 7525 |
rs777517254 | in-del | -/TGGT | | | intron-variant | YES1 | GRCh38.p7 | 18:779268 | ATCAGCCAAGCATGG[-/TGGT]TGGTACACACCTGTA | 7525 |
rs777589020 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:774715 | GAATTATTCTAATAG[A/C]CTAACTGGTCTCCCA | 7525 |
rs777592175 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:768029 | TCAAAATTGCTTTAA[A/C]TACTCTAGGGCAGGG | 7525 |
rs777600210 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:757869 | ATAAAATTATCTGTT[-/A]AAAAAAAAAAGAAAA | 7525 |
rs777649929 | snp | A/G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:788446 | TATGTACATAATAAC[A/G/T]ATGTGTATATATTTA | 7525 |
rs777656785 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:735281 | TGAGTGGATAAAAAA[A/C]AATGTGGCATATATA | 7525 |
rs777676589 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:755250 | GTCCTCTGGCCATTG[C/T]CTTTTTTTTTTTTTT | 7525 |
rs777694192 | snp | A/G | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775776 | CACTCCAGCCTGGGT[A/G]ACAGAGTGAGAACTT | 7525 |
rs777701383 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:789448 | ATTAGCCAAGTGTGG[C/T]AGTACAGGCCTGTAG | 7525 |
rs777706059 | snp | C/T | 1.64819e-05 | 0.00287066 | missense | YES1 | GRCh38.p7 | 18:724470 | TCTGTAGCAGTGAAG[C/T]AGTCTTCCAAGAAGG | 7525 |
rs777727650 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:724784 | ATTTTAAACATGAGA[A/G]TATCAAGAAGAGCTT | 7525 |
rs777753303 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:784068 | ACTGGCAAAAAAATA[A/T]TCATTTTAACACACA | 7525 |
rs777756615 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:803546 | CCTCATACTGTCCTA[C/T]AGGGTTAGAGTATGA | 7525 |
rs777763921 | snp | C/G | 1.65457e-05 | 0.00287621 | intron-variant | YES1 | GRCh38.p7 | 18:743252 | AAACAAAAATTCAGG[C/G]TTCTTACCCATCCAC | 7525 |
rs777841481 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:754574 | TTAGCCGGGTGCCGT[C/G]GTGTTTGTTTCTTGT | 7525 |
rs777880481 | snp | C/T | 1.64743e-05 | 0.00287 | missense | YES1 | GRCh38.p7 | 18:743326 | AAGATTCTCGAGGGA[C/T]TTCCCAAGCATCTTT | 7525 |
rs777885053 | snp | C/T | 1.65501e-05 | 0.00287659 | intron-variant | YES1 | GRCh38.p7 | 18:733013 | TTTTTAAAAATCTAT[C/T]TGTGTAAACATAGCA | 7525 |
rs777892520 | in-del | -/T | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723662 | TATATTGCCTTAAAA[-/T]AATCAATGCAACCTC | 7525 |
rs777959785 | in-del | -/GGGT | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813296 | GGACCCGGAAGGATG[-/GGGT]GGGTGGGGGCGTAAA | 7525 |
rs778034280 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:749457 | CAGCCAAGATCATGC[A/C]ATTGCACTCCAGCCT | 7525 |
rs778072540 | snp | C/G | 2.65883e-05 | 0.00364602 | intron-variant | YES1 | GRCh38.p7 | 18:746088 | TGAATTGAAAAGTAT[C/G]AGGTTCAGAAAAATT | 7525 |
rs778089345 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:734580 | ACAAAACAAAAAAAA[A/C]CAGGAGCAACTACAA | 7525 |
rs778102217 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:784465 | TCAGTGTCTATTAAT[C/T]ATTGCTGCTACAACA | 7525 |
rs778121763 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:759152 | GTATATTCTAAAGAT[A/G]TGAGTTAACTATAAG | 7525 |
rs778322511 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:772879 | TATCTTCCACAGCAC[G/T]TTAATTGCCTGTTTC | 7525 |
rs778323912 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:730477 | AGCCTCCCAAAGTGC[A/T]GGGATTATAGGAGTG | 7525 |
rs778341274 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:779307 | TACTCAGAAGGCTGA[A/G]GTGGGAGGACAGCTT | 7525 |
rs778358432 | in-del | -/T | 1.66983e-05 | 0.00288944 | intron-variant | YES1 | GRCh38.p7 | 18:756512 | ATATATTACCCAAGG[-/T]TGATGTTCTCAAACA | 7525 |
rs778363285 | snp | C/T | 0.000278022 | 0.011787 | intron-variant | YES1 | GRCh38.p7 | 18:745939 | ATACTAATATAACAA[C/T]ATTCATACCTTTAGT | 7525 |
rs778366513 | snp | C/T | 1.64909e-05 | 0.00287144 | synonymous-codon | YES1 | GRCh38.p7 | 18:724451 | TCCTGGCTGGTACTG[C/T]GGCTCTGTAGCAGTG | 7525 |
rs778375899 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:760191 | AGCATACAGGGGGAC[C/T]GGGCACAGTGGCTCA | 7525 |
rs778456524 | snp | A/C | 3.72766e-05 | 0.00431705 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724373 | TGTAGAAAATCTACA[A/C]AAGTTCTTTATATTT | 7525 |
rs778498724 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:755958 | AAAGGTTGTCAACAA[C/T]CACTTCTTGCTATTC | 7525 |
rs778500703 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:739053 | TGGTCTCGAACTCCT[A/G]ACCTCAAGTGACCCA | 7525 |
rs778504149 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:747770 | TATGACATTAGTTAT[G/T]AATTTTTAAGTAACA | 7525 |
rs778545464 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:789544 | ATGGTGACTATGCCA[C/T]TGCACTTCAGCCTAG | 7525 |
rs778557149 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:808139 | AAAGGTAAACCCAAC[A/G]CAGACCAGGATATAT | 7525 |
rs778635391 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:801786 | ACACTTGAAACAGTT[G/T]AGTGTAATAACTCAT | 7525 |
rs778695262 | in-del | -/AG | | | intron-variant | YES1 | GRCh38.p7 | 18:775021 | ATAGAGGTCAGAGAC[-/AG]AGTGTCTGGGTGCAA | 7525 |
rs778738989 | snp | A/G | 1.65312e-05 | 0.00287495 | | | GRCh38.p7 | 18:743007 | TGTCTTAATTTTTTC[A/G]TTATCTGAGCTTCTT | 7525 |
rs778757166 | snp | A/C | | | | | GRCh38.p7 | 18:727750 | TTACTGTCACAGTCT[A/C]TTTTTATATACATTA | 7525 |
rs778791817 | snp | C/T | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776063 | TTCTACTGGATGTAA[C/T]CTTGCAATAGATTGC | 7525 |
rs778845997 | snp | A/G | 1.6582e-05 | 0.00287936 | intron-variant | YES1 | GRCh38.p7 | 18:743235 | AGCTAAACAATGACA[A/G]AAAACAAAAATTCAG | 7525 |
rs778846706 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:777275 | TAATTGTTTTATATA[C/T]GTATATAAAGACATT | 7525 |
rs778898697 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:726134 | GCTTTCATTCAAAAC[C/T]TCACTCAAAGGCCGG | 7525 |
rs778901698 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:797000 | AAACAAAAACCTGTA[A/G]GTAGAATTTTTAACA | 7525 |
rs778925037 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:760341 | CACGTGTGGTGGTGC[A/G]CACCTGTAGTCCCCG | 7525 |
rs778947168 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:804366 | TAATCCCAATACTTT[A/G]GGAGGCCAAGGCAGG | 7525 |
rs778947408 | snp | A/T | 3.30508e-05 | 0.00406501 | intron-variant | YES1 | GRCh38.p7 | 18:733007 | AATTGTTTTTTAAAA[A/T]TCTATTTGTGTAAAC | 7525 |
rs779016332 | snp | C/T | 3.73183e-05 | 0.00431946 | intron-variant | YES1 | GRCh38.p7 | 18:745931 | TTATACTTATACTAA[C/T]ATAACAATATTCATA | 7525 |
rs779141765 | snp | A/C | 1.87598e-05 | 0.0030626 | missense | YES1 | GRCh38.p7 | 18:746043 | CTCCCCATTTTGCCA[A/C]AATACCATCTGGAAA | 7525 |
rs779213099 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:791454 | CCCTTTCAGTTAAGG[A/C]CTATTTTTACTCACC | 7525 |
rs779230964 | snp | C/G | 3.29457e-05 | 0.00405854 | missense, intron-variant | YES1 | GRCh38.p7 | 18:732864 | GGCCCTTTGTTACTA[C/G]TTCTGTTTGCAGAAT | 7525 |
rs779234636 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:786605 | AAAATTAATACCATA[C/T]CAGTTCAGGGTGGCA | 7525 |
rs779256213 | in-del | -/TTTAA | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723144 | ATGATTTGAAAACTG[-/TTTAA]GAGTTCTAAAAATGT | 7525 |
rs779266981 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:745115 | ACATCCCCTCTCCTA[C/G]TATTAATCATGTAAA | 7525 |
rs779356333 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:794484 | AGAATATTATTAGGA[C/T]AATTGGAAAAATATA | 7525 |
rs779388719 | snp | A/G | 1.85737e-05 | 0.00304738 | intron-variant | YES1 | GRCh38.p7 | 18:739820 | AAGCTTCCTGTAACA[A/G]ACAGCAAGATATTCA | 7525 |
rs779393155 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:795252 | TTGTTTTAGGAAATA[A/C]ATACTGAAATATTTA | 7525 |
rs779402740 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:768233 | CCTGCCAAACCATGC[A/G]TGAGGGTCTTTGCAT | 7525 |
rs779407325 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:789598 | AAAACAAAAACAAAA[A/G]CCCCCAAAACAAAAA | 7525 |
rs779429158 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:731425 | AACCAGACAAAGTGG[A/G]TGATAAAATTTGATG | 7525 |
rs779451004 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:761694 | GCCTCACACATCTAC[A/G]CACTTATCTTTCCAA | 7525 |
rs779507968 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:746276 | ATATTAACTACTCAA[C/T]GTGTCTCTCAAAACT | 7525 |
rs779520964 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:789616 | CCCAAAACAAAAAAA[A/C]CCAACAACGTTCTAC | 7525 |
rs779563120 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:742206 | CTCTAAGTACCATCT[A/G]CACAGGGAAAAAGAG | 7525 |
rs779568092 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:751217 | TCTACTTTCTACAAC[A/G]AGCATCAAATTTTCT | 7525 |
rs779576075 | snp | G/T | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776152 | TCTCACCAGCAAGCA[G/T]GAGAATTACCATTGC | 7525 |
rs779596788 | snp | C/T | 1.68049e-05 | 0.00289865 | missense | YES1 | GRCh38.p7 | 18:742963 | TTGGTTCTTCAGAAA[C/T]AACAGCATATAGTGG | 7525 |
rs779608640 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:741058 | ACAAGCCACCACGCC[A/C]AGCTGTTTTTTGTAT | 7525 |
rs779648075 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:734720 | ATGTTGGTGTGGATG[C/T]GGTGAAAAGGGAACA | 7525 |
rs779655460 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:727989 | TGGATTTTGGAATAT[C/T]TGCATATACATAATG | 7525 |
rs779663375 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:728901 | TTGATTTTTGTAATT[C/T]GACCATGATATGTTT | 7525 |
rs779672218 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:777562 | CTGTAATCCCAACAC[C/T]TTGGGAGGCTGAGGC | 7525 |
rs779705404 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:798557 | ATGCATAGGGGAGCC[A/G]CTTTAGCTCCACCCT | 7525 |
rs779712187 | snp | A/T | 3.34694e-05 | 0.00409067 | intron-variant | YES1 | GRCh38.p7 | 18:743210 | CATAAATTGTTGCAC[A/T]TTAATCCACAGCTAA | 7525 |
rs779772570 | snp | A/G/T | 6.58897e-05 | 0.00573945 | synonymous-codon, stop-gained, intron-variant | YES1 | GRCh38.p7 | 18:732849 | CTGGATATGGCACTC[A/G/T]GCCCTTTGTTACTAG | 7525 |
rs779800542 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:803262 | TAAATACCCATCTCA[C/T]TCCTAATTTTTCTGT | 7525 |
rs779819961 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:778993 | CTTTTTTCTGCCTTT[C/T]AGATATACAAACAAT | 7525 |
rs779856263 | snp | C/T | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775817 | AATTAAAAAAAAAAA[C/T]AGAATCATATATAAT | 7525 |
rs779877047 | snp | C/T | 1.64866e-05 | 0.00287106 | missense | YES1 | GRCh38.p7 | 18:756560 | TTTAAATCTCACCTG[C/T]TAAACCAGCAGGATA | 7525 |
rs779960794 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:784446 | GAACTCAGAATATTT[C/T]AGCTCAGTGTCTATT | 7525 |
rs779985915 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:766677 | TGACTACACCTTATT[C/T]TGAGCATGTTCTCAT | 7525 |
rs779987386 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:807088 | CAGCCTGGACAACAC[A/G]GTGAGACCCCATCTC | 7525 |
rs780007471 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:737820 | TATCTTCTGGGCTCA[A/G]GCAATTTTCCCACCT | 7525 |
rs780041460 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:785630 | CACAATGCAACAGTG[C/T]TGAGAGGTGGGATCT | 7525 |
rs780044402 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:795645 | TCATCCTCAGCAAAC[C/T]AACACAGGAACAGAA | 7525 |
rs780070603 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:729710 | CAGCTCACTGCAACC[A/T]CCACCTCCTGGGTTC | 7525 |
rs780075326 | snp | G/T | 1.83586e-05 | 0.00302968 | intron-variant | YES1 | GRCh38.p7 | 18:745910 | AAAATACTGCCCCAA[G/T]AAATTTTATACTTAT | 7525 |
rs780136264 | in-del | -/CTTG | 0.000164948 | 0.00908003 | intron-variant | YES1 | GRCh38.p7 | 18:732985 | AATAATGTTGACCAT[-/CTTG]CTTAATTGTTTTTTA | 7525 |
rs780218102 | in-del | -/C | | | intron-variant | YES1 | GRCh38.p7 | 18:741151 | ATCTGCCTGCCTCGG[-/C]CCTCCCAAAGCGCTG | 7525 |
rs780257636 | snp | A/C | 1.65759e-05 | 0.00287883 | intron-variant | YES1 | GRCh38.p7 | 18:724642 | CCATACCTAATACAC[A/C]AGATTAAAACATTAA | 7525 |
rs780288432 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:774514 | CTCGATAAATGTTAA[C/T]GCCATTCTTCTAGTT | 7525 |
rs780339856 | in-del | -/G | | | intron-variant | YES1 | GRCh38.p7 | 18:770713 | GTTTCCCTTCTTTTA[-/G]GGGATCACAGTCCTG | 7525 |
rs780347413 | snp | A/T | 1.64887e-05 | 0.00287125 | synonymous-codon | YES1 | GRCh38.p7 | 18:745769 | GGTTGTGATATAGTA[A/T]CCACCATTGTCAAGT | 7525 |
rs780424527 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:755252 | CCTCTGGCCATTGCC[-/T]TTTTTTTTTTTTTGG | 7525 |
rs780440409 | in-del | -/C | | | intron-variant | YES1 | GRCh38.p7 | 18:809772 | GATTCCTTAAAAAAA[-/C]AACAACAAATTCATG | 7525 |
rs780460362 | snp | A/C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:770754 | GTCCAAAGTCTAAAA[A/C/T]CCATTGTTTCATTAT | 7525 |
rs780509454 | in-del | -/CC | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812330 | TCCACCTCCTCCGCC[-/CC]CCCCCCCCGGCCCCG | 7525 |
rs780527959 | in-del | -/AC | | | intron-variant | YES1 | GRCh38.p7 | 18:765704 | CACCCGGCCAATTTA[-/AC]ACTTTTTAATAAGGA | 7525 |
rs780531770 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:755183 | TTAAGACTGTAATTG[A/T]CTTAACATGCATAAC | 7525 |
rs780602055 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:801939 | GTTTTGGACTTACTA[C/T]ATCATTTTCCATTAC | 7525 |
rs780679360 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:809210 | GTCTTCTGTGAAAAT[A/G]TTAAAACAATTAAGT | 7525 |
rs780703467 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:730752 | ACTTTTGTAGTTGTT[C/T]ACAGTGCTATAATAA | 7525 |
rs780717298 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:792360 | TTTTGGATTTGGGTT[-/A]AAAAAAATAAAATAA | 7525 |
rs780726492 | snp | A/G | 1.66032e-05 | 0.0028812 | intron-variant | YES1 | GRCh38.p7 | 18:756534 | TCTCAAACAGACAAC[A/G]TAATTGTCCATTTAA | 7525 |
rs780738904 | snp | C/T | 1.72892e-05 | 0.00294012 | intron-variant | YES1 | GRCh38.p7 | 18:739710 | CACTTTTAATTCAAA[C/T]GGATACATGTATATA | 7525 |
rs780808894 | in-del | -/AC | 1.843e-05 | 0.00303556 | intron-variant | YES1 | GRCh38.p7 | 18:736984 | AGAGAAAAACAAAAA[-/AC]ACAAGACATACGATA | 7525 |
rs780817872 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:766931 | ATAGGTTGCCTTTGC[A/G]TTTCCATAACAGTAT | 7525 |
rs780838371 | snp | A/G | 1.75173e-05 | 0.00295945 | missense | YES1 | GRCh38.p7 | 18:742935 | TTTGACATAAATTCA[A/G]TGACAATGTAAATTG | 7525 |
rs780949416 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:777679 | AGGCATGGTGGTGTG[C/T]GCCTGTAATCCCAGC | 7525 |
rs780995150 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:786907 | ATTTAAAAAAGCTCA[C/T]AGGAACCTAAGCCTG | 7525 |
rs781025903 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:752631 | TAACACTTAAAGATA[A/C]AAATGTCATGTTTTG | 7525 |
rs781052871 | in-del | -/A | 3.31005e-05 | 0.00406807 | splice-donor-variant | YES1 | GRCh38.p7 | 18:751702 | ATATTCATGACACTT[-/A]ACGTATTGTTAATTA | 7525 |
rs781057206 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:799903 | ACAAACAAACAAAAA[C/T]AAAAAACAAAAAAAA | 7525 |
rs781094110 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:779293 | CCTGTAGTCCTGGCT[A/C]CTCAGAAGGCTGAGG | 7525 |
rs781094238 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:806819 | CATGGTCTAACTGTA[C/T]CTCATCCTTCCTCTG | 7525 |
rs781097669 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:788188 | AGCATGAATGGTTTT[A/C]TTCTAGTTCAATAAA | 7525 |
rs781154670 | snp | A/G | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812999 | CCCCAGGAGCTTCCT[A/G]TTGACTGTAGGTCGA | 7525 |
rs781163459 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:751149 | GCAGACCATAAATAT[A/G]TATTTTGAGAAGTTA | 7525 |
rs781189252 | snp | A/G | 1.65127e-05 | 0.00287334 | synonymous-codon | YES1 | GRCh38.p7 | 18:745735 | TCACCAATTTCTGCA[A/G]AGTATCAAATTGTGC | 7525 |
rs781189639 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:784179 | TCTCATATTTAAGAA[G/T]AATTAAGATGAATAA | 7525 |
rs781191210 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon | YES1 | GRCh38.p7 | 18:724520 | TGGTCTTTCATCAGG[A/G]TCCTTCTTCCAACAC | 7525 |
rs781275703 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:796935 | AAAAATTACCTCACA[A/G]CATACATAAAATCCA | 7525 |
rs781354282 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:759531 | CGGTCTTTTGTATCT[A/C]TGAGTTCTGCATCCA | 7525 |
rs781426420 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:795779 | GGGAAGGGGAGGGAG[A/C]GCATTAGGAGAAATA | 7525 |
rs781440213 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:762274 | GCGGTGAGCCGAGAT[C/T]GCGTCATTGCACTCC | 7525 |
rs781450069 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:804115 | AAATATTAACTGTAT[G/T]TGTATAAAGACAAAT | 7525 |
rs781471917 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:758828 | CTCATCGCTTACCTA[C/T]CGTATTATCTATCAT | 7525 |
rs781492606 | snp | A/G | 1.69172e-05 | 0.00290832 | missense | YES1 | GRCh38.p7 | 18:736939 | TAGTTCATTCTTTCA[A/G]TATATGCCATACCAT | 7525 |
rs781497236 | snp | A/C | 1.64863e-05 | 0.00287104 | synonymous-codon | YES1 | GRCh38.p7 | 18:743381 | CACAGTTGGACACAC[A/C]GTTGTCAACTTGTGG | 7525 |
rs781501851 | snp | A/G | 2.1908e-05 | 0.00330961 | intron-variant | YES1 | GRCh38.p7 | 18:756880 | CAGTTAACACACAGG[A/G]TACTTCAAAAAGACA | 7525 |
rs781524022 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:807920 | TGAAATGAAGTATAA[C/T]GCTTCAAGGAACCTG | 7525 |
rs781542012 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:771302 | AACCTAGGAGGCGGA[C/G]GTTGCAGTGAGCCAA | 7525 |
rs781545266 | snp | A/G | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722920 | ACACGGTGAAACTGC[A/G]TCTCTACTAAAAATA | 7525 |
rs781588650 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:770574 | TGCCTCAGCTTCCAT[-/A]AATTCTGATCTCTAT | 7525 |
rs781614550 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:803380 | TCTTCTTTCCCTACC[C/G]AATGCCAAAGTGAGG | 7525 |
rs781657070 | snp | C/T | 1.66496e-05 | 0.00288522 | intron-variant | YES1 | GRCh38.p7 | 18:747885 | AAACATTTCAAAAAT[C/T]AAAATAATTAATAAA | 7525 |
rs781676799 | snp | A/G | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:814056 | TGGAGTTTTAAAGTT[A/G]GGAGAGTATGTCAGA | 7525 |
rs781683436 | snp | A/T | | | synonymous-codon | YES1 | GRCh38.p7 | 18:756645 | TGAGGATCCTCCAAA[A/T]GGTGTCATGGAAAGA | 7525 |
rs781763311 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:734511 | CAGTGAGCCAAGATC[A/G]CGCCACTGCACTCCA | 7525 |
rs781772142 | snp | A/G | 0.00019769 | 0.00994012 | intron-variant | YES1 | GRCh38.p7 | 18:748033 | CCTGCAACACATAAA[A/G]CAGCAATCACCGCAA | 7525 |
rs796100864 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:785358 | AAGGAAACAAGTCAA[C/T]AAGAGATATCATCTT | 7525 |
rs796163902 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:750021 | TTAAATAGGAAGATA[A/G]ATATGGGATTTGTTA | 7525 |
rs796191935 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:726633 | AAAAATATAAAAACT[A/G]ACTGGGCATGGTGGG | 7525 |
rs796224038 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:734472 | GCTTAGGCAGAATGG[C/T]GAGAACCCGGGAGGC | 7525 |
rs796315530 | in-del | C/TT | | | intron-variant | YES1 | GRCh38.p7 | 18:783619 | ATCAATTTTTCTCTT[C/TT]TTTTTTTTTTTTGAA | 7525 |
rs796353352 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:810099 | TAGTCTTCTTTCTTA[C/G]TATAATGCTAATAGA | 7525 |
rs796397849 | in-del | -/TA | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722009 | AAAATGAATACACAT[-/TA]AGTTAGTGTTTTATC | 7525 |
rs796463986 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:792868 | AAAGCCAAGGGGGGG[A/G]AAAAAGCTTAAATCA | 7525 |
rs796487904 | in-del | -/AATGATTTAAC | | | intron-variant | YES1 | GRCh38.p7 | 18:778466 | GACTAAAAATTTTCA[-/AATGATTTAAC]ACATTTCTGAACCTC | 7525 |
rs796512187 | in-del | -/AA | | | intron-variant | YES1 | GRCh38.p7 | 18:807332 | GAGTGATACTTCATC[-/AA]AAAAAAAAAAAAAAA | 7525 |
rs796544924 | in-del | -/TA | | | intron-variant | YES1 | GRCh38.p7 | 18:745598 | CATTTATTGGGCATG[-/TA]TTATGTGTAAATAAG | 7525 |
rs796612383 | in-del | -/G | | | intron-variant | YES1 | GRCh38.p7 | 18:725550 | ACTCAATACTTAAAA[-/G]GAAGTTTTCTGAGCT | 7525 |
rs796627826 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:786792 | TCTACCATAAAGTCA[A/G]ATATACCTGCATGTT | 7525 |
rs796657798 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:774505 | CTTCCCCAACTCGAT[-/A]AATGTTAACGCCATT | 7525 |
rs796673221 | in-del | -/G | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812566 | ATGGCGGCGGGGTCC[-/G]GGGCGGATTCCCGGG | 7525 |
rs796676822 | snp | C/T | | | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721454 | GAGGCAGGAGAATGG[C/T]GTGACCCCGGGAGGC | 7525 |
rs796684106 | in-del | -/ACACAC | | | intron-variant | YES1 | GRCh38.p7 | 18:786497 | CATTAATAAGTCCAT[-/ACACAC]ACACACACACACACA | 7525 |
rs796694837 | snp | C/T | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724130 | AAAGGAAATGATTTA[C/T]AAATAAGCAGGAGCC | 7525 |
rs796712513 | in-del | -/CA | | | intron-variant | YES1 | GRCh38.p7 | 18:783400 | GGGGAAACACACACA[-/CA]CACACACACACGGAA | 7525 |
rs796737426 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:804836 | GGAGAATCACTTGAA[C/T]CCAGGAGGCTGAGGT | 7525 |
rs796826797 | snp | A/T | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724152 | GCAGGAGCCTCACTG[A/T]CCTTCATTACCATGC | 7525 |
rs796833113 | in-del | -/AAAA | | | intron-variant | YES1 | GRCh38.p7 | 18:742473 | TTAAAAAAAAAAAAA[-/AAAA]GAAAGCAGTGGGGAA | 7525 |
rs796854037 | in-del | -/AC | | | intron-variant | YES1 | GRCh38.p7 | 18:732457 | AAAAAAAAAAAAAAA[-/AC]AAAACACCAATCACA | 7525 |
rs796860524 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:751329 | TTACCCAACTTTCTC[C/T]CCCTCCTTTTTTTTT | 7525 |
rs796883412 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:725305 | TCACGTCCTATCTCC[C/T]GCATCACCTTCCTTC | 7525 |
rs796926058 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:732236 | CTGAGGTCAGGAGTT[C/G]GAGACCAGCTTAGCC | 7525 |
rs796938577 | in-del | -/CA | | | intron-variant | YES1 | GRCh38.p7 | 18:783402 | GGAAACACACACACA[-/CA]CACACACACGGAAAA | 7525 |
rs796939569 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:749124 | CGAGATCATGCCACT[A/G]GACTCCAGCCTGGGC | 7525 |
rs796941381 | snp | A/G | | | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721404 | TTAGCCGGGCGTGGT[A/G]GCAGGCGCCTGTAGT | 7525 |
rs796949692 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:735114 | GTGAGCTGAGATTGT[A/G]CCACTGCACTCCAGC | 7525 |
rs796999422 | in-del | -/AC | | | intron-variant | YES1 | GRCh38.p7 | 18:786501 | AATAAGTCCATACAC[-/AC]ACACACACACACACA | 7525 |