| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs35605223 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157774880 | TTAATTCCCCCTAGT[-/A]CCCGTGAATGCAAGG | 51429 |
| rs35636059 | in-del | -/AA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157923441 | CTAAAAAAAAAATAA[-/AA]CCTGTCATTTACAGT | 51429 |
| rs35637138 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157902232 | AAAAAAAAGGATTTT[-/T]GATTTACAAGGTTAA | 51429 |
| rs35637213 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157830312 | AAAATTACCCTGGTC[-/C]TTGAAAGAGTTCTAG | 51429 |
| rs35650956 | in-del | -/CAG | 0.499839 | 0.00898417 | intron-variant | SNX9 | GRCh38.p7 | 6:157736005 | GCCTCTCAATGATTC[-/CAG]ACTGAAGATGTTTAT | 51429 |
| rs35655578 | in-del | -/A | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157865359 | AAAAAAAAAAAAAAA[-/A]CACCACATAACATGA | 51429 |
| rs35663087 | in-del | -/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893653 | ACTCAAATAAAGGGG[-/G]AAGACTTGCTATTTC | 51429 |
| rs35682523 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157738465 | GATTGCAACCCCTGC[-/T]TTTTTTTTTCTTTCC | 51429 |
| rs35689483 | in-del | -/T | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157891296 | AGCCTCCCAAAATGT[-/T]GGGATTACAAGTGTG | 51429 |
| rs35701745 | snp | A/T | 0.295854 | 0.245759 | intron-variant | SNX9 | GRCh38.p7 | 6:157817561 | TGTGGGGCTTTTAGC[A/T]TTAAAAGTAGCACTT | 51429 |
| rs35704898 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157754322 | GTTCAGCTTACGCCC[-/C]AGGAATGAACACAGA | 51429 |
| rs35710238 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157730232 | AAAAAAAAAAAAAAA[-/A]GAATGAAGGAGCCAG | 51429 |
| rs35729102 | snp | G/T | 0.376989 | 0.215346 | intron-variant | SNX9 | GRCh38.p7 | 6:157716479 | TGGAGTGGCAGGGCT[G/T]GGCTCATGTTGAGGC | 51429 |
| rs35731152 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157748251 | CTCTGTATCTAGTTT[-/T]AGTTTTGATCATATT | 51429 |
| rs35735079 | in-del | -/T | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157730214 | CTGTTTTTTTTTTTT[-/T]AAAAAAAAAAAAAAA | 51429 |
| rs35741590 | in-del | -/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157753757 | GTAACCGCCCAAGGG[-/G]TTCACCTTGCCCCGC | 51429 |
| rs35760729 | in-del | -/GA | 0.375 | 0.216506 | intron-variant | SNX9 | GRCh38.p7 | 6:157934314 | ATGATTATAGGGAAG[-/GA]GAGAGAGAGATGGAA | 51429 |
| rs35770455 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157847400 | AGCCACTGCGCCCAG[-/T]CCTTGTAGTACTTAT | 51429 |
| rs35770736 | snp | C/T | 0.292523 | 0.246357 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821762 | AAACACATAGGTTGC[C/T]TTCTGGTTGGAGTTA | 51429 |
| rs35778664 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157778570 | TGAGGATAAGGACAT[-/A]GTTATCATCATAAGA | 51429 |
| rs35787395 | in-del | -/G | | | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822223 | TCAAATAGAATGTAT[-/G]TTAAGAAGACACAAA | 51429 |
| rs35795546 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157941390 | GCAGCCTTTGCTTTT[-/T]GTGAATGAGGTTTTC | 51429 |
| rs35841473 | in-del | -/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157931252 | GAGGTACCACAGGGG[-/G]TACAATTTATTAAAA | 51429 |
| rs35866781 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157835436 | TTTTTTTTTTAAATA[-/A]GAGTCTTGCTCTGTT | 51429 |
| rs35868597 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157735971 | AAAAAAAAAAAAAAA[-/A]ATCCCACCTGAGCCT | 51429 |
| rs35888965 | in-del | -/A | 0.471578 | 0.115772 | intron-variant | SNX9 | GRCh38.p7 | 6:157789194 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 51429 |
| rs35919557 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157734074 | ATATAATAATATTTT[-/T]AGGATAAGAATATTG | 51429 |
| rs35949336 | in-del | -/G | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157877282 | AAAGAAAAAAAAAGC[-/G]GGGGGGGGCATCTAG | 51429 |
| rs36051765 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157914925 | AAGGTTTTAGGCTTT[-/A]TCGTTTAGATCTTTG | 51429 |
| rs36052795 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157932927 | CATTTCAAGGAAAAA[-/A]TGTTTGACCAAGTAA | 51429 |
| rs36061569 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157866659 | CCAGCACACACTGCC[A/C]TATGTAAGTCTTGGT | 51429 |
| rs36063627 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | SNX9 | GRCh38.p7 | 6:157876768 | TGCCGTTTGAGGCCC[C/T]GCGCCCTTTCCTAGT | 51429 |
| rs36063725 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157731961 | GGGAAGCAGGAGCCC[-/C]AATCACCAAAGGCCA | 51429 |
| rs36070508 | in-del | -/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157768000 | AGGGAGTAGGGGGAT[-/G]CTACTCTTCCTGGTT | 51429 |
| rs36075956 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157836834 | TGACCTCGTGATCCG[-/C]CCCACCTTGTCCTCC | 51429 |
| rs36086845 | snp | A/G | 0.296619 | 0.245615 | intron-variant | SNX9 | GRCh38.p7 | 6:157819366 | GTGAGGACGTCATAC[A/G]TTTATTAGGATTGGA | 51429 |
| rs36104407 | in-del | -/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157924369 | ATGTGCTGAAGGTGG[-/G]AGCTGTGGGTCTCCT | 51429 |
| rs36189425 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157739717 | GCCCATCAATGATAG[-/T]ACTGCATAAAGAAAA | 51429 |
| rs41268575 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157928516 | GCAAGAAAACAAGTG[C/T]CTGTGGTTATATTTG | 51429 |
| rs41268577 | snp | A/G | 0.0115144 | 0.0749975 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157943827 | TGGCCACGGCACACT[A/G]CTTGGCTTGGGTGGC | 51429 |
| rs41268579 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157944521 | CAGTAAATTCTCAAA[A/G]CACTTTTTCAAAACA | 51429 |
| rs41268581 | snp | A/G | 0.0185938 | 0.0946107 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157945051 | AGCTGTAGTCATACA[A/G]TCACATAACTTTTAC | 51429 |
| rs45440492 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157931980 | GTAGGAGTGATTGTC[A/G]GTAATAATAGCATCC | 51429 |
| rs45546633 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | SNX9 | GRCh38.p7 | 6:157937339 | TAATTTAGTGTAGCA[C/T]ATGCAGGATTTATAG | 51429 |
| rs55635614 | snp | G/T | 0.179744 | 0.239925 | intron-variant | SNX9 | GRCh38.p7 | 6:157770577 | CAGATCACGAGGTCA[G/T]GAGATCGAGACCACC | 51429 |
| rs55765743 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | SNX9 | GRCh38.p7 | 6:157717880 | GCACAGTGGTGAAAT[C/T]GGGGCTTTCAGTATG | 51429 |
| rs55838627 | snp | A/G | 0.310632 | 0.242536 | intron-variant | SNX9 | GRCh38.p7 | 6:157733480 | GCAAGACTCTATCTC[A/G]AAAAAAAAAAAAATG | 51429 |
| rs55901229 | snp | A/T | 0.206029 | 0.246103 | intron-variant | SNX9 | GRCh38.p7 | 6:157826855 | ATTATATTTTATATA[A/T]AAATATATATTATAG | 51429 |
| rs55927736 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157723577 | AATCTATCATTCAGG[C/T]TCAGCCCTTGGAGGT | 51429 |
| rs55976134 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157785022 | GAGGCCGAGGCGGGC[A/G]GATCACGAGGTCAGG | 51429 |
| rs56099739 | snp | A/G/T | 0.00518141 | 0.0506816 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890193 | TTTATCCCATATTGT[A/G/T]TATTTGTACCATGTG | 51429 |
| rs56166671 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157744763 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTTGC | 51429 |
| rs56213734 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SNX9 | GRCh38.p7 | 6:157830604 | GTGCTGTTCAGTGTA[C/T]TCTTTGTGATGATGT | 51429 |
| rs56282226 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157879829 | TCAGATTACTGCTTC[C/T]TTAGAGTACTTACTT | 51429 |
| rs56284081 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157844523 | GTTTAGAGAGGATCA[A/G]AATCTTGTAGCCTCC | 51429 |
| rs56303673 | in-del | -/AA | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889450 | AAAAAAAAAAAAAAA[-/AA]GACACCAAAGGATCC | 51429 |
| rs56322641 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157851753 | CGCTACCACACCCAG[C/T]TAATTTTTTGTATTT | 51429 |
| rs56340437 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157734624 | TGTCTTATCATTATA[A/G]GATTTATGGCTCTTT | 51429 |
| rs56396531 | in-del | -/AA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157902977 | CTAGCCAAAAAAAAA[-/AA]GTTTTTAACAGTACT | 51429 |
| rs56409318 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157895958 | AATAAGGAGTCCCCT[C/T]TGCTTTAACCCTTAC | 51429 |
| rs56729794 | in-del | -/CACACA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157818096 | ACACACACACACACA[-/CACACA]CATATATATATATAC | 51429 |
| rs56859515 | snp | A/T | 0.24019 | 0.249807 | intron-variant | SNX9 | GRCh38.p7 | 6:157804756 | GCACTTAACCAAACA[A/T]CTGAGTACCATGGCC | 51429 |
| rs56895176 | snp | A/C | 0.0356815 | 0.128715 | intron-variant | SNX9 | GRCh38.p7 | 6:157733086 | GGCCACCTGAGGGGA[A/C]TTCCAGCGTTTCCCA | 51429 |
| rs56930644 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157856575 | ATAATCATTTCTGCA[A/G]TTGGACTCAGAATCC | 51429 |
| rs56967435 | snp | A/G | 0.0788843 | 0.182262 | intron-variant | SNX9 | GRCh38.p7 | 6:157805029 | ATAATTTTTCTTTAC[A/G]AAGGACTTGTAAGTT | 51429 |
| rs57012276 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157838153 | AAGTAGCTGGGACTA[C/T]AGGCATGCATCACCA | 51429 |
| rs57078179 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | SNX9 | GRCh38.p7 | 6:157753103 | ATTTTTCTTAGTACA[A/G]AACAAAATGGAGTCT | 51429 |
| rs57181144 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | SNX9 | GRCh38.p7 | 6:157756050 | ATCACATCTGATGAC[A/C]GTAAATGTCAGTCTC | 51429 |
| rs57207307 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157902224 | CTTAAAAAAAAAAAA[-/A]GGATTTTTGATTTAC | 51429 |
| rs57272349 | in-del | -/CCT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840430 | TTTCTTTTCTTTCTT[-/CCT]TTCTTTCCTTTCTTT | 51429 |
| rs57273513 | in-del | -/GTT/GTTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157759852 | ATCAAAGTTTGTTTT[-/GTT/GTTT]TTTTGTTTGTTTGTT | 51429 |
| rs57283917 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157898993 | CATTTGTCTCTCGGC[C/T]TCTCCATAATGGCAC | 51429 |
| rs57333702 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157932894 | AAAAAAAAAAAAAAA[-/A]GCCAGATTTCATCAA | 51429 |
| rs57335143 | in-del | -/CTTCCTTTC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840442 | CTTTTCTTTCCTTTC[-/CTTCCTTTC]TTTCCTTTCCTTCCT | 51429 |
| rs57422766 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157933403 | TGTTGATCCTGATAC[A/T]CAAGGCAGACAGTGC | 51429 |
| rs57547404 | in-del | -/GGGAGGAAGGAGAAGGAGGAGAGCCCACAGGGGAGGAAGGAGAAGGAGGAGAGCCCACAG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157899141 | GAGGAGAGCCCACAG[lengthTooLong]CACCTTATCTGACAC | 51429 |
| rs57597968 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157777379 | AAAAAAAAAAAAAAA[-/A]GGCAAAAGCAGTCAG | 51429 |
| rs57637207 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | SNX9 | GRCh38.p7 | 6:157876555 | TTTTTGTAGACATTC[C/T]GAATTACAAATTAGA | 51429 |
| rs57674908 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157899635 | AAAAATTAGCCGGGT[A/G]TGGTGGCAGGCGCCT | 51429 |
| rs57709608 | snp | C/T | 0.0908922 | 0.192833 | intron-variant | SNX9 | GRCh38.p7 | 6:157760052 | TTTTTATCTTTTTTT[C/T]AGTAGAGATGGGGTT | 51429 |
| rs57831745 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157838201 | TATTTTTTATAGAGA[C/T]GGTGTTTTGCCATGT | 51429 |
| rs57834462 | snp | A/G | 0.387074 | 0.209071 | intron-variant | SNX9 | GRCh38.p7 | 6:157731016 | TTATTATTTCTGAGA[A/G]AGAGTCTTGCTCTGT | 51429 |
| rs57845814 | in-del | -/AA | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157753249 | AAAAAAAAAAAAAAA[-/AA]GAGGGAGTACAGCAG | 51429 |
| rs57885108 | in-del | -/TGTG/TGTGTGTGTG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157734256 | GTGTGTGTGTGTGTG[-/TGTG/TGTGTGTGTG]CTTTCATGATTTCTT | 51429 |
| rs57976405 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | SNX9 | GRCh38.p7 | 6:157896511 | GATACAGGTTCAGAA[A/C]AGTAGTGGTTACTTC | 51429 |
| rs57991215 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157838193 | AATTTTTGTATTTTT[A/T]ATAGAGATGGTGTTT | 51429 |
| rs58068231 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | SNX9 | GRCh38.p7 | 6:157768067 | AGGCCCAGGTACTTC[C/T]TCAGTCCCAGGTGAA | 51429 |
| rs58317565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157798412 | TCTAGATTGATGAAG[A/G]TCAAAGAGGAATGAG | 51429 |
| rs58463899 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SNX9 | GRCh38.p7 | 6:157795062 | GAAACTGAACAATCA[C/T]ATGCAGTATGTGCAC | 51429 |
| rs58526057 | in-del | -/T | 0.24019 | 0.249807 | intron-variant | SNX9 | GRCh38.p7 | 6:157805015 | GATAACCAAAAAAAA[-/T]AATTTTTCTTTACGA | 51429 |
| rs58640753 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | SNX9 | GRCh38.p7 | 6:157941252 | CAGCTCCTTCCCCCC[A/G]TCACAGCCTCTCTGT | 51429 |
| rs58660308 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | SNX9 | GRCh38.p7 | 6:157732641 | TAGTCACATTGCTGT[A/G]TATAAGATCCCCAGA | 51429 |
| rs58693731 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157775373 | CAAAAAAAAAAAAAA[-/A]CTTAAGCAGCAGGCT | 51429 |
| rs58771051 | in-del | -/GACT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840390 | ACACCCAAAATGACT[-/GACT]TTTACAAAAAATACT | 51429 |
| rs58879069 | snp | C/G/T | 0.0626037 | 0.165477 | intron-variant | SNX9 | GRCh38.p7 | 6:157790070 | GGCAGGGAGGACGGG[C/G/T]GCATCCACTCCCTCT | 51429 |
| rs59022017 | in-del | -/TC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157870258 | CTCTCACCTGCTCTC[-/TC]ACATCCCCACGCTCA | 51429 |
| rs59162713 | snp | A/G | 0.175576 | 0.238665 | intron-variant | SNX9 | GRCh38.p7 | 6:157770584 | CGAGGTCAGGAGATC[A/G]AGACCACCCTGGCTA | 51429 |
| rs59233831 | snp | C/T | 0.371987 | 0.218218 | intron-variant | SNX9 | GRCh38.p7 | 6:157900531 | GTCCGGGGGGGTCAC[C/T]GCCTTCTGGTCCTGC | 51429 |
| rs59298856 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157838215 | ATGGTGTTTTGCCAT[A/G]TTGCCCAGGCTGGTC | 51429 |
| rs59303332 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | SNX9 | GRCh38.p7 | 6:157780061 | GACATTCCAAGGGCC[A/G]GCTCTGAGGCCAGCC | 51429 |
| rs59317121 | in-del | -/T | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157826916 | TATATAATATATAAA[-/T]ATATATTATAGTTTA | 51429 |
| rs59331733 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157838194 | ATTTTTGTATTTTTT[A/G]TAGAGATGGTGTTTT | 51429 |
| rs59341606 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157902224 | ACTTAAAAAAAAAAA[-/A]GGATTTTTGATTTAC | 51429 |
| rs59343355 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157904581 | TAATCCCCACAGAAG[C/T]GCACCTGTAGTCCCA | 51429 |
| rs59479920 | in-del | -/A | 0.488241 | 0.0757703 | intron-variant | SNX9 | GRCh38.p7 | 6:157750761 | TCTACAACTCAACAG[-/A]AAAAAAAAAAACCCT | 51429 |
| rs59483949 | snp | A/G | 0.0777841 | 0.181223 | intron-variant | SNX9 | GRCh38.p7 | 6:157780409 | TTTGGCCTCTGGTTG[A/G]GTGTGCCTCCATCCT | 51429 |
| rs59553691 | in-del | -/CAACCCTCCGGTTATCATCCTGAGATGGGACAGCCTTTGTGA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157733921 | GGACAGCCTTTGTGA[lengthTooLong]GGGGAGAAACTCTCT | 51429 |
| rs59593756 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SNX9 | GRCh38.p7 | 6:157925254 | ATGTGTAGAAAAGTA[C/T]CTAATCTCATTAGCA | 51429 |
| rs59622734 | in-del | -/A | 0.422 | 0.181428 | intron-variant | SNX9 | GRCh38.p7 | 6:157729102 | GAGCAAGACTCCATC[-/A]AAAAAAAAAAAAAAA | 51429 |
| rs59643482 | in-del | -/TCATCTGTA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157798175 | TGATCAAAGTTAATA[-/TCATCTGTA]ATGAAATAAATGGAA | 51429 |
| rs59644010 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157827089 | TATATAATATATAAA[C/T]ATATATTATAGTTTA | 51429 |
| rs59769554 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840428 | TCTTTCTTTTCTTTC[-/C]TTTTCTTTCCTTTCT | 51429 |
| rs59827439 | in-del | -/AATAAATAAATAAAAA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157817900 | ATAAATAAATAAATA[-/AATAAATAAATAAAAA]GCACTTGAGCCCTGG | 51429 |
| rs59894271 | in-del | -/TCTTT/TCTTTCGT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840405 | ACTTTTACAAAAAAT[-/TCTTT/TCTTTCGT]ACTTTCTTTCTTTCT | 51429 |
| rs59951233 | snp | A/G | 0.115744 | 0.21191 | intron-variant | SNX9 | GRCh38.p7 | 6:157770615 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAAAA | 51429 |
| rs60039604 | snp | C/T | 0.296109 | 0.245711 | intron-variant | SNX9 | GRCh38.p7 | 6:157819103 | CAACTAAAACAAACA[C/T]AATTTTAAAACCATA | 51429 |
| rs60058086 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | SNX9 | GRCh38.p7 | 6:157920591 | AGTTCAGTTCTTCAA[A/G]CATAAACACTTCTCA | 51429 |
| rs60192571 | in-del | -/GTTTG | 0.488965 | 0.0734569 | intron-variant | SNX9 | GRCh38.p7 | 6:157759853 | TCAAAGTTTGTTTTT[-/GTTTG]TTTGTTTGTTTGTTT | 51429 |
| rs60209306 | snp | G/T | 0.210909 | 0.246925 | intron-variant | SNX9 | GRCh38.p7 | 6:157759848 | ATGCCATCAAAGTTT[G/T]TTTTTTTTGTTTGTT | 51429 |
| rs60217709 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157826971 | TTTATATAATATATA[-/C]ATATATATTATAGTT | 51429 |
| rs60230845 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157800690 | TTATGATAGCTATTA[A/C]ATGTATATTACTTTT | 51429 |
| rs60286364 | in-del | -/C | 0.0425829 | 0.139564 | intron-variant | SNX9 | GRCh38.p7 | 6:157831229 | TTTGATTTGATTTTT[-/C]CTTGAGTTGCTTGTT | 51429 |
| rs60317272 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822055 | AATGTTGGCCTCCCA[A/G]TATTTTTTTTTACGG | 51429 |
| rs60317827 | in-del | -/A/AA | 0 | 0 | upstream-variant-2KB, downstream-variant-500B | SNX9, LOC107986663 | GRCh38.p7 | 6:157715058 | TAAAAAAAAAAAAAA[-/A/AA]GAAGAAGAAGAAGCA | 51429 |
| rs60345349 | snp | A/G | 0.0581099 | 0.160244 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893701 | CAGTACTGAAATATT[A/G]TGGAGTGAAAGGCAT | 51429 |
| rs60482949 | snp | C/T | 0.24019 | 0.249807 | intron-variant | SNX9 | GRCh38.p7 | 6:157813578 | CTCAGGAGTTGTCAG[C/T]AGTGTGCTTTGGGTC | 51429 |
| rs60593905 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | SNX9 | GRCh38.p7 | 6:157797888 | GATGCAATGAGATGC[C/T]ACAATAAATAAGCGT | 51429 |
| rs60690391 | in-del | -/AATAAATAAATAAATAAATA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157769067 | ATAAATAAATAAATA[-/AATAAATAAATAAATAAATA]CACACTTAATAGCAA | 51429 |
| rs60828875 | snp | C/T | 0.24019 | 0.249807 | intron-variant | SNX9 | GRCh38.p7 | 6:157804799 | CACATAACATAATCA[C/T]CCCAGCATCCAGTTG | 51429 |
| rs60831221 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157940823 | ACTGAGCAGAGAAAC[C/T]AGGTGTTGTCATTTG | 51429 |
| rs60997523 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157824039 | GTTTTGCTACCTTTT[-/T]CATTGTGAATGGCAT | 51429 |
| rs61011738 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157899643 | GCCGGGTGTGGTGGC[A/G]GGCGCCTGTAGTCCC | 51429 |
| rs61033762 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | SNX9 | GRCh38.p7 | 6:157732879 | CCAACATCTCTCCAT[C/T]TCTGCCATCCTTGCC | 51429 |
| rs61039577 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157867784 | TCATTCAAACCCACA[G/T]GATTTTTTTCCTGTT | 51429 |
| rs61140176 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SNX9 | GRCh38.p7 | 6:157770718 | AGGCAGGAGAATGGC[A/G]TGAACCTGGGAGGCA | 51429 |
| rs61145963 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157899783 | CGTCTCAAAAAAAAA[-/A]TTATCTATATTTGAG | 51429 |
| rs61195155 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157734411 | GGGGATTGGATGGCA[A/G]GATGGCAATTTACAA | 51429 |
| rs61219852 | snp | A/T | 0.0452528 | 0.143452 | intron-variant | SNX9 | GRCh38.p7 | 6:157770744 | AGGCAGAGCTTGCAG[A/T]GAGCCGAGATCGCGC | 51429 |
| rs61266434 | snp | A/T | 0.146985 | 0.227789 | intron-variant | SNX9 | GRCh38.p7 | 6:157770930 | AAGACAATTTGTGAA[A/T]ATACCTATGCTTATA | 51429 |
| rs61268876 | in-del | -/CCT | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888637 | CCTTCTTCTCCTTCT[-/CCT]TCTCCTTCTTCCATA | 51429 |
| rs61277554 | in-del | -/T/TTTTTT | 0 | 0 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894127 | TTTTTTTTTTTTTTT[-/T/TTTTTT]GAGACAGAGTCTCTC | 51429 |
| rs61282095 | snp | A/C | 0.209693 | 0.246729 | intron-variant | SNX9 | GRCh38.p7 | 6:157778940 | CTCCTGCCGGGAGGG[A/C]AGCCGATGAGCTGGA | 51429 |
| rs61328457 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | SNX9 | GRCh38.p7 | 6:157842258 | CTGGTTGACATTTGT[A/G]TGAGTCTGCCCATGT | 51429 |
| rs61389131 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | SNX9 | GRCh38.p7 | 6:157756016 | TAACATCAGCTGACT[A/G]ACAAGATGTTTGCCA | 51429 |
| rs61458171 | in-del | -/T | 0.337386 | 0.23423 | intron-variant | SNX9 | GRCh38.p7 | 6:157721656 | CTCTCCTCTGACCTC[-/T]CCGTCCACTCCTCCC | 51429 |
| rs61484959 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SNX9 | GRCh38.p7 | 6:157770317 | TTCCTGCTCGCCAGC[C/T]ATGGAGACAGGAGAC | 51429 |
| rs61521541 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157838169 | AGGCATGCATCACCA[C/T]GCCTGGCTAATTTTT | 51429 |
| rs61526278 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SNX9 | GRCh38.p7 | 6:157782534 | GTAACTACTAAAAAA[C/T]GCAAAGAGGCAAAAA | 51429 |
| rs61556222 | in-del | -/AGA | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157892047 | GATGGACAGTTAAGA[-/AGA]GCTTTGCAAAATAAG | 51429 |
| rs61636568 | snp | C/T | 0.301429 | 0.244653 | intron-variant | SNX9 | GRCh38.p7 | 6:157771136 | TGACTAAGAATAACT[C/T]AGTCATTTATGACTA | 51429 |
| rs61658593 | snp | A/C | 0.00755907 | 0.0610114 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157944501 | AATTGTTTAAAAAAA[A/C]TGTACAGTAAATTCT | 51429 |
| rs61701164 | snp | A/C | 0.235854 | 0.249599 | intron-variant | SNX9 | GRCh38.p7 | 6:157804912 | TCCACCAATACCACC[A/C]ATGAGGGGGGTGCCC | 51429 |
| rs61736723 | snp | A/C | 6.60469e-05 | 0.00574622 | missense | SNX9 | GRCh38.p7 | 6:157896878 | GCCTCCAAATCTGGG[A/C]ACTGGGAAAGCTCAG | 51429 |
| rs61748681 | snp | A/G | 0.0172974 | 0.0913755 | missense | SNX9 | GRCh38.p7 | 6:157901963 | TCTTCCTACTTTAAG[A/G]ATTCAGAGTCAGCTG | 51429 |
| rs62423463 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157800432 | TGCTTGAGCCCAGGA[A/G]TTTGAGACCAATCTG | 51429 |
| rs62423464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157803934 | GCATGATCTTGGCTC[A/G]CTGCAATCTCTGCCT | 51429 |
| rs62423465 | snp | C/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157814949 | AAGTTTCAGTGAAGG[C/G]TTGGAGGCTGGGTCT | 51429 |
| rs62423466 | snp | C/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157814953 | TTCAGTGAAGGCTTG[C/G]AGGCTGGGTCTGATT | 51429 |
| rs62423467 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157815217 | GCCAGGGCTGTCTGT[G/T]GGTTTTTTTTTTTTA | 51429 |
| rs62423468 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157827529 | CATATAGTTTATATA[A/T]TATATAAACATATAT | 51429 |
| rs62423469 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157827542 | TAATATATAAACATA[A/T]ATTATATTATAGTTT | 51429 |
| rs62423470 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157827544 | ATATATAAACATATA[C/T]TATATTATAGTTTAT | 51429 |
| rs62423472 | snp | A/G | 0.046775 | 0.145601 | intron-variant | SNX9 | GRCh38.p7 | 6:157854754 | TACCCCCTTTTATGT[A/G]GCCTTTAATGCAGAT | 51429 |
| rs62423473 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157854973 | AAAAAAAAAAAACCC[A/C]ACAACACTACAAAAG | 51429 |
| rs62423475 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157897167 | AGCAGCTGTGCAGCA[G/T]ACACCAGCTGAGTGT | 51429 |
| rs62423476 | snp | A/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157941154 | CCCTTTGCTTTTTGG[A/G]TAACACTGGGTTAAA | 51429 |
| rs62424626 | snp | G/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157758092 | AGGAGGATCACTTGA[G/T]CCCAGGAGTTCAAAG | 51429 |
| rs62424627 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157784365 | ATAGTTATCAAAAGG[A/T]ATTTTTTTTTTTTTT | 51429 |
| rs62424628 | snp | A/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157794962 | TTTGGAAGAGCAGAA[A/T]TTAAAAAAAAAAAAA | 51429 |
| rs62647325 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157827348 | TTTATATAATATATA[A/C]ACATATATTATAGTT | 51429 |
| rs62647326 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157827377 | TTTATATAATATATA[A/C]ACATATATTATAGTT | 51429 |
| rs62772067 | snp | A/T | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157901868 | TCTTTTTTTTTTTTT[A/T]AACTGATGATCTTCC | 51429 |
| rs63379260 | snp | A/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157784367 | AGTTATCAAAAGGAA[A/T]TTTTTTTTTTTTTTT | 51429 |
| rs66471126 | in-del | -/TTT | 0.375 | 0.216506 | intron-variant | SNX9 | GRCh38.p7 | 6:157819832 | TTGTATTCTAGCTGC[-/TTT]TTTTTTTTTTTTTTT | 51429 |
| rs66514647 | in-del | -/TGAC | 0.0592355 | 0.161582 | intron-variant | SNX9 | GRCh38.p7 | 6:157840385 | TCACCACACCCAAAA[-/TGAC]TGACTTTTACAAAAA | 51429 |
| rs66670568 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157929784 | ATAATTTTAAAGAGA[-/C]GGAAACTAAATATGG | 51429 |
| rs66740717 | in-del | -/CTCAGCCTCCCAA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157913426 | AGTGATCCTCCCACG[-/CTCAGCCTCCCAA]TAGCTGGGATTATAG | 51429 |
| rs66795570 | in-del | -/A/TTT | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157923439 | TGTAAATGACAGGTT[-/A/TTT]TTTTTTTTTTAGATT | 51429 |
| rs66921004 | in-del | -/GGGTGTCTTTGGATCTCGGGAAAGAGCAGACCCTCAGGCTGGTGCTTG | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157840251 | TCAGGCTGGTGCTTG[lengthTooLong]CACAGTGAGGCCAGA | 51429 |
| rs66921733 | in-del | -/TATATC | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157873639 | GTCATATTATAAATA[-/TATATC]TATATTTATAATTTA | 51429 |
| rs67147465 | snp | A/G | 0.26518 | 0.249539 | intron-variant | SNX9 | GRCh38.p7 | 6:157850699 | TCATTGTCAAGCTCC[A/G]TACATCTGATAATGC | 51429 |
| rs67186551 | in-del | -/T | 0.5 | 0 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157891049 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCAC | 51429 |
| rs67261471 | in-del | -/GAGA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157744004 | CCTGGGTGATAGAGA[-/GAGA]CTCTGTCTTAAAAAA | 51429 |
| rs67414769 | in-del | -/GT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157781826 | GTGTATGTGTGTGTG[-/GT]TGTGTGTGTGTGTGT | 51429 |
| rs67464115 | in-del | -/T | 0.402982 | 0.197728 | intron-variant | SNX9 | GRCh38.p7 | 6:157827863 | AGGAGTTCCTGATGC[-/T]TTTTTTTTTTTTTTA | 51429 |
| rs67470291 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157826788 | TAAATATATTATATT[-/A]TATATATATATTATA | 51429 |
| rs67838864 | in-del | -/T | | | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821598 | GTGTCACATATTTCC[-/T]TTTTTTTTTTTTTTT | 51429 |
| rs67846531 | in-del | -/CACA | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157734251 | AAGAAATCATGAAAG[-/CACA]CACACACACACACAC | 51429 |
| rs68043397 | in-del | -/A | 0.219947 | 0.248187 | intron-variant | SNX9 | GRCh38.p7 | 6:157878889 | AGATGAAGAATTCAG[-/A]GAAAAATAGGTAAAG | 51429 |
| rs71027366 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157744024 | AATTTTTTCTTTTTT[-/T]TTTTTTTTAAGACAG | 51429 |
| rs71027367 | in-del | -/AGAA | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157780710 | GAAAGAGAGAGAGAG[-/AGAA]AGAAAGAAAGAAAGA | 51429 |
| rs71027369 | in-del | -/AAAAAAC | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157834150 | AAAAAAAAAAAAAAA[-/AAAAAAC]CACAGTGGACACCAC | 51429 |
| rs71027370 | in-del | -/A | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157834530 | TCAATTCTACTAAAG[-/A]AAAAAAAAATTTAAA | 51429 |
| rs71027371 | in-del | -/TT | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157926803 | AGAAACACCCTATAC[-/TT]TTTTTTTTTTTTTTT | 51429 |
| rs71542908 | in-del | -/AAT | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157740102 | AATAATAATAATAAT[-/AAT]AAATCTTTATTTAAC | 51429 |
| rs71551124 | snp | G/T | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157833798 | ATGATTTTACAGTTG[G/T]TTTGTTGATGCATCA | 51429 |
| rs71558064 | in-del | ACT/CC | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157938783 | GCTGGGGAAAAAAAA[ACT/CC]TCCACCAGCACCTCA | 51429 |
| rs71563719 | snp | G/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157722228 | TTCTTCTATTCTCTG[G/T]CATCCAAAGGTCAAA | 51429 |
| rs71563720 | snp | A/C | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157770643 | AAAAATAATAATAAT[A/C]CAAAAAATTAGCCAG | 51429 |
| rs71563721 | snp | C/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157818096 | ACACACACACACACA[C/T]ACACACATATATATA | 51429 |
| rs71563722 | snp | C/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157834071 | TGCTGGAGGCATAAT[C/T]TGACTGGATCCTGCC | 51429 |
| rs71563723 | snp | C/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157834110 | ACACCAGGGCTTGAT[C/T]TGATTGGATTTTGGA | 51429 |
| rs71563724 | snp | A/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157834539 | TTTTTTTCTTTAGTA[A/G]AATTGAGGTCTCGCC | 51429 |
| rs71563725 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | SNX9 | GRCh38.p7 | 6:157839998 | TTCTGAAAGCAGGTG[A/G]AAAAAAACAAGAAAG | 51429 |
| rs71563726 | snp | A/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157850088 | GAAGGAAGAAAACCA[A/G]AGGAGGGCAGGTGTG | 51429 |
| rs71563727 | snp | A/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157914886 | AGGTGTCATGGCTAA[A/G]AGCAGTTCACAACAT | 51429 |
| rs71563728 | snp | C/T | 0.104859 | 0.203554 | intron-variant | SNX9 | GRCh38.p7 | 6:157942115 | TCATCACTGTCTTTG[C/T]ATAAACCTAAGTAGC | 51429 |
| rs71667211 | in-del | -/AG | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157934323 | TGATTATAGGGAAGG[-/AG]AGAGAGAGATGGAAG | 51429 |
| rs71676201 | in-del | -/TCTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157780716 | CTTTTCTGTTTCTTT[-/TCTT]CTTTCTTTCTTTCTT | 51429 |
| rs71682274 | in-del | -/AA | 0.293807 | 0.246132 | intron-variant | SNX9 | GRCh38.p7 | 6:157816030 | TTAAAGTATAATAAT[-/AA]AAAAAAAAGCAGCAG | 51429 |
| rs71689763 | in-del | -/CA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157927931 | ACACACACACACACA[-/CA]TAACCCTTCAACCAC | 51429 |
| rs71708505 | in-del | -/GTAAGCTGTCTCT | 0.135484 | 0.22223 | intron-variant | SNX9 | GRCh38.p7 | 6:157810378 | TCCACTGTGGGGGTG[-/GTAAGCTGTCTCT]ATATATTTCAAAACT | 51429 |
| rs71723229 | in-del | -/AAG | 0.144296 | 0.226554 | upstream-variant-2KB, downstream-variant-500B | SNX9, LOC107986663 | GRCh38.p7 | 6:157715057 | CTTAAAAAAAAAAAA[-/AAG]AAGAAGAAGAAGCAG | 51429 |
| rs71774697 | in-del | -/T | 0.115438 | 0.210697 | intron-variant | SNX9 | GRCh38.p7 | 6:157797694 | TGGGCCTGGAATATC[-/T]TTTTGTGCCAGAAAA | 51429 |
| rs71788446 | in-del | -/A/AA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157923429 | AGAAATTGAAAATCT[-/A/AA]AAAAAAAAAATAACC | 51429 |
| rs71795443 | in-del | -/ATTAT | 0.132751 | 0.2208 | intron-variant | SNX9 | GRCh38.p7 | 6:157884282 | GAGATTTTCCATGTA[-/ATTAT]ATTTGTTGCAAAGGA | 51429 |
| rs71813906 | in-del | -/A | | | upstream-variant-2KB, downstream-variant-500B | SNX9, LOC107986663 | GRCh38.p7 | 6:157715045 | GAGACTCCGTCTCTT[-/A]AAAAAAAAAAAAAGA | 51429 |
| rs71825015 | in-del | -/TGTGTG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157734219 | TCAGTTTAGGATTTA[-/TGTGTG]TGTGTGTGTGTGTGT | 51429 |
| rs71826849 | in-del | -/AT | 0.153665 | 0.230694 | intron-variant | SNX9 | GRCh38.p7 | 6:157820671 | ATTGTGAAAGTGCAC[-/AT]GTTTATCTCTTTTTT | 51429 |
| rs71856428 | in-del | -/ATA | 0.499839 | 0.00898417 | intron-variant | SNX9 | GRCh38.p7 | 6:157740094 | CCCAGAACTTAAAGT[-/ATA]ATAATAATAATAATA | 51429 |
| rs71901542 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157721288 | CCACCTCAAAAAAAA[-/A]AAAAAATTATAGCAG | 51429 |
| rs72099435 | in-del | -/TG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157734219 | TCAGTTTAGGATTTA[-/TG]TGTGTGTGTGTGTGT | 51429 |
| rs72260397 | in-del | -/ACTT | 0.0322114 | 0.122752 | intron-variant | SNX9 | GRCh38.p7 | 6:157866044 | CTGTGAAAGACAATC[-/ACTT]AGAATTTGAAAAGGA | 51429 |
| rs72267618 | in-del | -/CTG | 0.326506 | 0.238006 | intron-variant | SNX9 | GRCh38.p7 | 6:157919465 | GGTGTTTTTTTTCTT[-/CTG]CTACCTTAAATCTTA | 51429 |
| rs72567437 | snp | A/G | 0.387074 | 0.209071 | intron-variant | SNX9 | GRCh38.p7 | 6:157730922 | GGGATTACAGGCATT[A/G]GCCACTGTGCCCGGC | 51429 |
| rs72567468 | snp | C/T | 0.210605 | 0.246877 | intron-variant | SNX9 | GRCh38.p7 | 6:157795548 | ATAGCATTATGATTA[C/T]ATAAGAAAATATCCT | 51429 |
| rs73014826 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | SNX9 | GRCh38.p7 | 6:157742210 | GGAAGAGAAGAAATC[C/T]CCCAGCCAGCATCTG | 51429 |
| rs73014870 | snp | C/T | 0.304937 | 0.243889 | intron-variant | SNX9 | GRCh38.p7 | 6:157762032 | TGGAGTGGGGCGCAC[C/T]GCAGGGAGCACGGCC | 51429 |
| rs73018952 | snp | C/T | 0.323434 | 0.238972 | intron-variant | SNX9 | GRCh38.p7 | 6:157763354 | GGATCTCCAGGCCTT[C/T]TCCATGGAATTTAGA | 51429 |
| rs73018966 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157773301 | GCCAGGGTGCTAGGC[C/T]CCAGCTACACTGTGG | 51429 |
| rs73018968 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157773437 | GCAGGTGAGCCAGGC[A/G]ACCTCGGCAGGAGCC | 51429 |
| rs73020603 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157793404 | TATTCCCCATCCCCC[A/G]CCAAGTTTTTATTCA | 51429 |
| rs73020626 | snp | A/G | 0.148326 | 0.228391 | intron-variant | SNX9 | GRCh38.p7 | 6:157808024 | GGCAGAATAAAATAT[A/G]AGATACTTCCCAAAG | 51429 |
| rs73020632 | snp | C/T | 0.149999 | 0.229128 | intron-variant | SNX9 | GRCh38.p7 | 6:157811486 | AATAAAAAAGCATTA[C/T]TGGAGTAGAGGCTAA | 51429 |
| rs73020633 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157812595 | AAAGTGGGTGTAAAT[C/G]GTTTCCCTCCTCCCC | 51429 |
| rs73020638 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SNX9 | GRCh38.p7 | 6:157814273 | AATGTCATAATCTGT[C/T]CTCTAGCCATCCTTC | 51429 |
| rs73020642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157814779 | GAGTCAGTAACCATG[A/G]TACAAAAATATTCAC | 51429 |
| rs73020649 | snp | A/G | 0.146314 | 0.227484 | intron-variant | SNX9 | GRCh38.p7 | 6:157818617 | TCTCCAAGGACTCAC[A/G]CCAGCCTGTCCTTAA | 51429 |
| rs73020653 | snp | C/G | | | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822081 | TACGGAGAAAGACAA[C/G]TATTTATGCATATTA | 51429 |
| rs73020657 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157824891 | TTTGAGGTTTGTTGC[C/G]AGACATTCCAGAAAT | 51429 |
| rs73022621 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SNX9 | GRCh38.p7 | 6:157828798 | GGTCTTAATGCGTCT[A/G]AGCATCACTTCCCCG | 51429 |
| rs73022635 | snp | A/G | 0.241914 | 0.249869 | intron-variant | SNX9 | GRCh38.p7 | 6:157840241 | AGAGCAGACCCTCAG[A/G]CTGGTGCTTGCACAG | 51429 |
| rs73022638 | snp | A/G | 0.182933 | 0.240836 | intron-variant | SNX9 | GRCh38.p7 | 6:157840294 | CAGGGAAGAGGGGCT[A/G]CTCCCCAGGCTGAGG | 51429 |
| rs73022676 | snp | C/T | 0.103438 | 0.202533 | intron-variant | SNX9 | GRCh38.p7 | 6:157859739 | GGCCATTGTATTCTT[C/T]AATGAACTGTTTGTT | 51429 |
| rs73024635 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | SNX9 | GRCh38.p7 | 6:157863019 | ACACTGTTTCTCTTT[A/G]TCATTCTGTGCTACA | 51429 |
| rs73024638 | snp | A/T | 0.143284 | 0.226079 | intron-variant | SNX9 | GRCh38.p7 | 6:157863656 | CCACATGGAAAATAG[A/T]TGGCAGTTGGGGTTG | 51429 |
| rs73024642 | snp | C/T | 0.150333 | 0.229274 | intron-variant | SNX9 | GRCh38.p7 | 6:157865500 | GCCATGATCTCCACT[C/T]GGGTCCCAGCCTCCA | 51429 |
| rs73024644 | snp | A/C | 0.029116 | 0.117091 | intron-variant | SNX9 | GRCh38.p7 | 6:157866654 | CTCGACCAGCACACA[A/C]TGCCCTATGTAAGTC | 51429 |
| rs73024666 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887801 | AGAATAATACCACCG[C/T]TTATTTCACAGGAGA | 51429 |
| rs73026650 | snp | A/G | 0.125874 | 0.217008 | intron-variant | SNX9 | GRCh38.p7 | 6:157897106 | AGCACAACACAGAAC[A/G]GTTTTGTGACCACAG | 51429 |
| rs73026678 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157909265 | GGTATTGTTGAAAAA[C/T]CAAAATGTGTAATGT | 51429 |
| rs73026690 | snp | C/T | 0.131038 | 0.219882 | intron-variant | SNX9 | GRCh38.p7 | 6:157913568 | GTACAGTTCTGAGTT[C/T]TGACAGCTACCACTG | 51429 |
| rs73026699 | snp | G/T | 0.350109 | 0.229081 | intron-variant | SNX9 | GRCh38.p7 | 6:157917624 | GATACCAAAATCCAT[G/T]GATGCTCAAGTCCCT | 51429 |
| rs73028512 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SNX9 | GRCh38.p7 | 6:157919871 | TACCTCTCTGAAGGT[G/T]GTTGTTTCTGCTTTT | 51429 |
| rs73571993 | snp | C/G | 0.199254 | 0.244796 | intron-variant | SNX9 | GRCh38.p7 | 6:157814279 | ATAATCTGTCCTCTA[C/G]CCATCCTTCTAGACT | 51429 |
| rs73571995 | snp | A/T | 0.0501905 | 0.150254 | intron-variant | SNX9 | GRCh38.p7 | 6:157815595 | AAAATGCGTTTTTCA[A/T]GACTGAGCTTATCTC | 51429 |
| rs73571997 | snp | G/T | 0.160938 | 0.233598 | intron-variant | SNX9 | GRCh38.p7 | 6:157816392 | GTTTACTAAAAAGGA[G/T]ATTTTGCATTTTGAC | 51429 |
| rs73571999 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | SNX9 | GRCh38.p7 | 6:157817012 | AAAGAGATCCCACCG[C/T]GCTTGTTCACCCTTC | 51429 |
| rs73573803 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | SNX9 | GRCh38.p7 | 6:157818906 | GCCTCCAGTCTCTCT[C/T]TGCCCATGCCAACTG | 51429 |
| rs73573804 | snp | C/G | 0.0648419 | 0.167978 | intron-variant | SNX9 | GRCh38.p7 | 6:157818974 | TCTGCTCAATTTCTA[C/G]TTCTGGACACTATGT | 51429 |
| rs73573809 | snp | A/G | 0.29278 | 0.246313 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821869 | TGGGTCCAAGGCTAC[A/G]GTCATTTTCGATTTG | 51429 |
| rs73573814 | snp | G/T | 0.119978 | 0.213528 | intron-variant | SNX9 | GRCh38.p7 | 6:157831035 | GAAATTGTATTTGGT[G/T]CTATTTCAAATCTGC | 51429 |
| rs73573818 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | SNX9 | GRCh38.p7 | 6:157836174 | AGGCTGATCTTGAAC[C/T]TCTGGGCTCAAACAT | 51429 |
| rs73573819 | snp | A/T | 0.0418186 | 0.138422 | intron-variant | SNX9 | GRCh38.p7 | 6:157839345 | AATAAAAGAGAAATT[A/T]TGTCTTTTATTAGAG | 51429 |
| rs73573821 | snp | C/G | 0.0460142 | 0.144533 | intron-variant | SNX9 | GRCh38.p7 | 6:157840486 | CTTCTCTCTCTCTCT[C/G]TCTTTCTTTCTCTTT | 51429 |
| rs73573823 | snp | A/G | 0.0818113 | 0.184966 | intron-variant | SNX9 | GRCh38.p7 | 6:157840687 | TTTAAGTCAATCAGT[A/G]AGAGAGCTTCAGAAG | 51429 |
| rs73573824 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | SNX9 | GRCh38.p7 | 6:157841940 | TGTGTACTCATCACC[C/T]ACCTCCACAGTGATC | 51429 |
| rs73573834 | snp | A/C | 0.244205 | 0.249933 | intron-variant | SNX9 | GRCh38.p7 | 6:157851268 | CTCAAAAAAAAAAAA[A/C]ACCCTAAAATAAATA | 51429 |
| rs73573836 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | SNX9 | GRCh38.p7 | 6:157852730 | TACAGATGCAGACCA[C/T]CATGCCCGGCTAATT | 51429 |
| rs73573842 | snp | A/T | 0.0618563 | 0.164627 | intron-variant | SNX9 | GRCh38.p7 | 6:157856162 | TGTCGATTTTATTTC[A/T]TAAAGTCTCCTCTAC | 51429 |
| rs73573849 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | SNX9 | GRCh38.p7 | 6:157867442 | ACAGCCACAGCCACT[A/G]TCATGTTTGTACCAG | 51429 |
| rs73573852 | snp | C/G | 0.0429648 | 0.14013 | intron-variant | SNX9 | GRCh38.p7 | 6:157869551 | CCCTAGAGTTTTACT[C/G]TGTCCAGCCTCTTCT | 51429 |
| rs73573861 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157870889 | CACCCGTGCAAGCAC[A/G]CACACACCCCTCAGA | 51429 |
| rs73573867 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | SNX9 | GRCh38.p7 | 6:157876936 | GCAAAGCCAAGCCAG[C/T]TGAGATTCACTGAGT | 51429 |
| rs73573870 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | SNX9 | GRCh38.p7 | 6:157878391 | TGGAGAAAATAATAG[A/G]CAGCATTTTTTTTAT | 51429 |
| rs73573873 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | SNX9 | GRCh38.p7 | 6:157879178 | TCCTGCAGATCTGCT[C/T]GCAGAACGCAGGTTT | 51429 |
| rs73575704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157910732 | AGTATGCAGGTAGAA[A/G]GGGTTTGTTTTTGTG | 51429 |
| rs73577616 | snp | A/T | 0.0581099 | 0.160244 | intron-variant | SNX9 | GRCh38.p7 | 6:157914970 | TATTTTTGTATAAGG[A/T]GTGCAGTGTGGTAGA | 51429 |
| rs73577622 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | SNX9 | GRCh38.p7 | 6:157929219 | TCCTGCCTCCCTCCT[C/T]CTCCTTTGTTTGTAG | 51429 |
| rs73577624 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | SNX9 | GRCh38.p7 | 6:157931082 | CTGGCCTCAGGCCGC[C/T]CTTTTGTGGGGTGGG | 51429 |
| rs73581767 | snp | A/C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, nc-transcript-variant | SNX9, LOC107986663 | GRCh38.p7 | 6:157714141 | GGAAGAGATGTTCTA[A/C/T]CTGCCAGGAGCTCCA | 51429 |
| rs73581787 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SNX9 | GRCh38.p7 | 6:157727069 | TGTGTAAGAGGTTAG[A/G]AGAAATCTGGGTATG | 51429 |
| rs73585964 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157764583 | AAAGAAAAAAAATCC[C/G]GATGTTTTTGTCATA | 51429 |
| rs73585977 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | SNX9 | GRCh38.p7 | 6:157775560 | CTCATGTCCTACCAT[A/T]GACTGACTTTACAGT | 51429 |
| rs73585987 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | SNX9 | GRCh38.p7 | 6:157777579 | TAACTATACAGTGGC[A/G]CCCTTGTCTGATGAA | 51429 |
| rs73587911 | snp | A/G | 0.0618563 | 0.164627 | intron-variant | SNX9 | GRCh38.p7 | 6:157792788 | GCTCAGTGTTTTAAA[A/G]GAGCATGTGTTAATT | 51429 |
| rs73587914 | snp | C/G | 0.0554779 | 0.157039 | intron-variant | SNX9 | GRCh38.p7 | 6:157796700 | TTGTCATTACATGCT[C/G]CGTAGATGTATTGAT | 51429 |
| rs73589921 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SNX9 | GRCh38.p7 | 6:157796724 | TATTGATCATCCATC[C/T]ATGCAAAAACTATTT | 51429 |
| rs73792125 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157788305 | GAAAAAGCCTGGAGG[A/T]TCTTTTAGCAGTTTA | 51429 |
| rs73792131 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157803377 | GGTTCTGTACCTAAG[A/G]GAAAAGTTGTTCTTA | 51429 |
| rs73792139 | snp | A/G | 0.0592355 | 0.161582 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821993 | TTATAAGGATTAAAT[A/G]AGATGGGGATGTGGA | 51429 |
| rs73792148 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | SNX9 | GRCh38.p7 | 6:157848249 | AAATATAAACATACC[A/G]GCTACCTAGCTTCAA | 51429 |
| rs73792150 | snp | C/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157855600 | TTTCATTTTATATTC[C/T]TTTCTGAGTACAGTT | 51429 |
| rs73792153 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | SNX9 | GRCh38.p7 | 6:157862939 | TCATGAGGAGATACA[C/T]TGGCTCCAGTAACAG | 51429 |
| rs73792154 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | SNX9 | GRCh38.p7 | 6:157869575 | CTCTTCTCTCCACCC[C/T]GCGCTTCCTGCCAGC | 51429 |
| rs73792155 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | SNX9 | GRCh38.p7 | 6:157883606 | TCAGTGTGGCTACCC[A/G]TCATCACCTTATCTT | 51429 |
| rs73792156 | snp | C/G | 0.137527 | 0.223271 | intron-variant | SNX9 | GRCh38.p7 | 6:157911968 | GAGTGGTCCCTCGTG[C/G]TGCTGGGGCGGTGGA | 51429 |
| rs73792157 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | SNX9 | GRCh38.p7 | 6:157929689 | CTCAGCATAGGAAAG[A/G]GATCTGTTCTTGTAA | 51429 |
| rs73794836 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | SNX9 | GRCh38.p7 | 6:157740691 | AGAATGAATCCACAA[C/T]TGTTGGAGAAAAGAG | 51429 |
| rs73794837 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | SNX9 | GRCh38.p7 | 6:157740722 | CTCACAACTGCCATT[A/G]GTTTCCCACAGTTAG | 51429 |
| rs73794839 | snp | A/C | 0.0341408 | 0.126114 | intron-variant | SNX9 | GRCh38.p7 | 6:157743230 | CTTTATTTGTATTTT[A/C]GGGTTTAGTTCTCTG | 51429 |
| rs73794846 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | SNX9 | GRCh38.p7 | 6:157756476 | CTCTGTAAATTGCGA[A/G]GCTCTACATAAGTAT | 51429 |
| rs73794847 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | SNX9 | GRCh38.p7 | 6:157756734 | TAAGCAAAGAAAACC[A/G]GGCCCCCGAGACGCA | 51429 |
| rs73794855 | snp | C/G | 0.0696718 | 0.173152 | intron-variant | SNX9 | GRCh38.p7 | 6:157760437 | CCCCCAGAGAGTGTC[C/G]AAAGGTTCAAATCGC | 51429 |
| rs73794856 | snp | C/G | 0.17461 | 0.238362 | intron-variant | SNX9 | GRCh38.p7 | 6:157760445 | GAGTGTCCAAAGGTT[C/G]AAATCGCAAAGTAGG | 51429 |
| rs73794857 | snp | C/G | 0.0640965 | 0.167152 | intron-variant | SNX9 | GRCh38.p7 | 6:157761027 | ACATGAATCACCCTC[C/G]TATGAATCACTAGTT | 51429 |
| rs73794858 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | SNX9 | GRCh38.p7 | 6:157766164 | CCTACTGAGTCCTCC[A/G]TCCACTCACAATGAT | 51429 |
| rs74326771 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | SNX9 | GRCh38.p7 | 6:157935757 | CCGGTGAAAGCGGGT[C/T]GGGGTGTAGACGAAC | 51429 |
| rs74330812 | snp | A/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157784949 | CAACTCTTAGGAAAT[A/T]GAAAAGAAAAGCAAA | 51429 |
| rs74359943 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SNX9 | GRCh38.p7 | 6:157830181 | GTGTCTTTGCTTACT[A/G]TTTCTTCTTACATTT | 51429 |
| rs74367387 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | SNX9 | GRCh38.p7 | 6:157872845 | ACACAGACAAGATGA[A/G]GGTCATCTAATCATC | 51429 |
| rs74424174 | snp | A/C | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157915823 | GAGTTAGACTCTGTC[A/C]AAAAAAAAAAAAAGA | 51429 |
| rs74427874 | snp | A/T | | | upstream-variant-2KB, downstream-variant-500B | SNX9, LOC107986663 | GRCh38.p7 | 6:157715045 | GAGACTCCGTCTCTT[A/T]AAAAAAAAAAAAAGA | 51429 |
| rs74428079 | snp | A/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157756429 | GTCTAAAAAAAAAAA[A/G]AGAGTTAAATTGGAA | 51429 |
| rs74430964 | snp | C/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157926601 | AGCCTGGCTAACACA[C/G]TGAAACCCCATCTCT | 51429 |
| rs74472184 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SNX9 | GRCh38.p7 | 6:157863505 | GACAATATATATTGA[A/G]TATATAGTTTGGAGT | 51429 |
| rs74543858 | snp | A/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157826966 | TATAGTTTATATAAT[A/G]TATAAACATATATTA | 51429 |
| rs74545334 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | SNX9 | GRCh38.p7 | 6:157920094 | AAGTTGGGGCTCCTG[C/T]CCTCTGTCAATGTAA | 51429 |
| rs74611316 | snp | A/T | 0.0471551 | 0.14613 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888928 | CTCTGTGGTTGACTG[A/T]GAGGAGGAGTGTGGT | 51429 |
| rs74700120 | snp | G/T | 0.0596104 | 0.162024 | intron-variant | SNX9 | GRCh38.p7 | 6:157820658 | TTCGGTGTGGCTTAT[G/T]GTGAAAGTGCACATG | 51429 |
| rs74703384 | snp | G/T | 0.0429648 | 0.14013 | intron-variant | SNX9 | GRCh38.p7 | 6:157877909 | TATCCAACTTCCTGA[G/T]TGTCGTATTTTTCTT | 51429 |
| rs74754638 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | SNX9 | GRCh38.p7 | 6:157769114 | CAACACAAGCAGTGG[A/G]CACTTTGGTGAGCAG | 51429 |
| rs74759507 | in-del | -/TTT | | | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821612 | CTTTTTTTTTTTTTT[-/TTT]ACATAAATGTACCAT | 51429 |
| rs74775779 | snp | A/G | 0.103438 | 0.202533 | intron-variant | SNX9 | GRCh38.p7 | 6:157760938 | TCTGGCAACACAGCC[A/G]GGGGAAAAGAGATTT | 51429 |
| rs74794277 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SNX9 | GRCh38.p7 | 6:157796941 | TCTAGAAGGTATTAT[A/G]TATTATAAATACTTA | 51429 |
| rs74868443 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | SNX9 | GRCh38.p7 | 6:157733964 | AAAGACATGACAATC[A/G]TCACCCTTGGAAAGA | 51429 |
| rs74871677 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | SNX9 | GRCh38.p7 | 6:157806269 | TAAAGCCATCATCTC[C/T]TTATTTCTTTTCCTC | 51429 |
| rs74894396 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | SNX9 | GRCh38.p7 | 6:157750915 | AAAACCACAATGAGC[A/T]AGCACTTCACACCTG | 51429 |
| rs74960680 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | SNX9 | GRCh38.p7 | 6:157742291 | TGTTTGGGAAGGAAG[C/T]TATTACGGGTTGGGA | 51429 |
| rs75047128 | snp | G/T | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157828510 | TTATTATTTTTTTTT[G/T]GGAGACAGGGTCTCA | 51429 |
| rs75055083 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157881721 | TTTGGCTTAAAGGAA[G/T]GTTGTAGCTGGTTTG | 51429 |
| rs75056612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157765647 | GGCGTAGGCCACCGC[A/G]CCCCGCCTGAAATGT | 51429 |
| rs75061556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157729969 | GAACAGGCAAATCTG[C/T]AGAGATAGACAGTAG | 51429 |
| rs75062032 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | SNX9 | GRCh38.p7 | 6:157717638 | ACACCAAGGTCTTAC[C/G]CACAGGAAGTGCTCC | 51429 |
| rs75122480 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | SNX9 | GRCh38.p7 | 6:157935491 | AGGCACCAGGGCACA[C/T]GACAAATTCAACACC | 51429 |
| rs75137982 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890067 | GCAGGCTTTGAGCCT[A/G]AGTTCTTAACCACTA | 51429 |
| rs75141517 | snp | C/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157827864 | GGAGTTCCTGATGCT[C/T]TTTTTTTTTTTTTAA | 51429 |
| rs75167222 | snp | C/G | 0.0460142 | 0.144533 | intron-variant | SNX9 | GRCh38.p7 | 6:157911427 | AAGAGTCGAGAGAAA[C/G]AGTTCAGGGAGGGCC | 51429 |
| rs75171630 | snp | A/G/T | 0.0209541 | 0.100278 | intron-variant | SNX9 | GRCh38.p7 | 6:157753833 | GAAAGAGTAATATAC[A/G/T]CAGAGCCGGCTGTAT | 51429 |
| rs75235583 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887059 | TTTCATGTCTGATAA[A/G]TTATGAGTGGATGTC | 51429 |
| rs75260229 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SNX9 | GRCh38.p7 | 6:157929122 | TAGTAGTAGAAAATA[C/T]GTCACAGCAGAAGCA | 51429 |
| rs75322805 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | SNX9 | GRCh38.p7 | 6:157902610 | CTAAAAACGTGGTCC[A/G]GAGCTTTGTGTTAGC | 51429 |
| rs75329869 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157881990 | TTCAGAGCAGATGAA[A/T]CAGCCTTCTATTATT | 51429 |
| rs75345612 | snp | A/C | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157770800 | AGCGAGACTCCTTCT[A/C]AAAAAAAAAAAAAAA | 51429 |
| rs75347841 | snp | A/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157784052 | CATAAATGAGTAGAG[A/G]AAAAAATTACAACTT | 51429 |
| rs75377635 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant | SNX9 | GRCh38.p7 | 6:157745275 | TACGTTATTGTGAGA[A/T]GTAGAAATTCTACAT | 51429 |
| rs75411130 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157732406 | CCCCTAATTTATTTC[A/C]TCATCTTTATTAAGG | 51429 |
| rs75426492 | snp | A/G | 0.120674 | 0.21395 | intron-variant | SNX9 | GRCh38.p7 | 6:157765244 | TATTTATGGGCAAGT[A/G]TTTGGGCATGGATAT | 51429 |
| rs75430829 | in-del | -/TTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157771720 | TTTTTTTTTTTTAAG[-/TTT]ATGGAGTCTCACTCT | 51429 |
| rs75460808 | snp | C/G | 0.0707826 | 0.174302 | intron-variant | SNX9 | GRCh38.p7 | 6:157781323 | GCTTCTGGGTGATGT[C/G]ACCACCTGCTCTGTT | 51429 |
| rs75462624 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | SNX9 | GRCh38.p7 | 6:157904896 | TGAATAGAATCACAA[A/G]ATATGCTCAAAATGC | 51429 |
| rs75468754 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157785536 | AGGATAAAAACCACA[C/T]GATCATTTCACAGAT | 51429 |
| rs75471009 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | SNX9 | GRCh38.p7 | 6:157924293 | TGGAGGAGAATACCT[A/G]TGAAACAAGATTGGC | 51429 |
| rs75479896 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157749283 | TGCAGTCAGGGTCTG[G/T]TTTGGCTCTTAGGTT | 51429 |
| rs75502429 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157766353 | ATCTTTCCTATTGCT[G/T]GACTCAAAATGTGTA | 51429 |
| rs75504650 | snp | A/G | 0.115788 | 0.21092 | intron-variant | SNX9 | GRCh38.p7 | 6:157726366 | TGTCTCTCCTTAACT[A/G]TTTGAACATACAGAA | 51429 |
| rs75511370 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | SNX9 | GRCh38.p7 | 6:157920018 | TTGCTCCTGTGTCTG[C/T]GGATTGGTAGTAAGC | 51429 |
| rs75542106 | snp | A/G | 0.040671 | 0.13668 | intron-variant | SNX9 | GRCh38.p7 | 6:157762097 | TCTCACAAGCTCAGG[A/G]TGCCCTGTGGGGCCG | 51429 |
| rs75545040 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157914189 | CATTTTAACCAGTCC[A/G]ATAGGTATGCAGTGG | 51429 |
| rs75560492 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SNX9 | GRCh38.p7 | 6:157827730 | AAATTGTTAGTGGAG[A/G]TTAATCCATATCTAT | 51429 |
| rs75583569 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | SNX9 | GRCh38.p7 | 6:157929065 | TTGGTAAGATGTTGT[A/G]TATTTGACTAAAACC | 51429 |
| rs75584447 | snp | A/C | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157770802 | CGAGACTCCTTCTCA[A/C]AAAAAAAAAAAAAGA | 51429 |
| rs75587153 | snp | A/C | 0.00100942 | 0.0224431 | missense | SNX9 | GRCh38.p7 | 6:157867616 | AATGAAGGAGAAATC[A/C]TCACAATCACAAATC | 51429 |
| rs75589634 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | SNX9 | GRCh38.p7 | 6:157796223 | GATAAATCTCACACA[C/T]GTTATTTCCTTAAAC | 51429 |
| rs75597730 | snp | A/T | 0.0452528 | 0.143452 | intron-variant | SNX9 | GRCh38.p7 | 6:157905309 | AAGCAATGCGACTGG[A/T]ACTTCGTAGAAATAA | 51429 |
| rs75607824 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157798171 | CAAGTGATCAAAGTT[A/G]ATATCATCTGTAATG | 51429 |
| rs75616448 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157812357 | CACAAATACATGTCC[A/T]ATTAATCAAAGAGCT | 51429 |
| rs75620218 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | SNX9 | GRCh38.p7 | 6:157814082 | GAAGGGAAGGGAGGA[A/C]ATTTTTCAGAATAGT | 51429 |
| rs75653462 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SNX9 | GRCh38.p7 | 6:157803249 | CATAATTCTTTCCAA[C/T]ATGGTTTCAAAACTG | 51429 |
| rs75662577 | snp | C/G | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157730178 | TGAACTCTATGCAGC[C/G]TGAATTATATCTTAG | 51429 |
| rs75665067 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SNX9 | GRCh38.p7 | 6:157933545 | CATGTCTTACAGTTG[A/G]CACTTTTAGACCAGA | 51429 |
| rs75670926 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | SNX9 | GRCh38.p7 | 6:157930246 | GCATACCAGCTGTTC[A/G]TGCTTGAGGGGCAGA | 51429 |
| rs75673735 | snp | A/C | 0.142272 | 0.225598 | intron-variant | SNX9 | GRCh38.p7 | 6:157848206 | ACAGCATTCATGGTA[A/C]TAACTGCCTATTCAA | 51429 |
| rs75693647 | snp | C/T | 0.104859 | 0.203554 | intron-variant | SNX9 | GRCh38.p7 | 6:157917686 | CTATGCACATTCTCC[C/T]GTATATTTTAAATCA | 51429 |
| rs75791415 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | SNX9 | GRCh38.p7 | 6:157851574 | CTAGGTATCTCACAT[A/G]GTGGAATCATATATT | 51429 |
| rs75851781 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | SNX9 | GRCh38.p7 | 6:157762043 | GCACCGCAGGGAGCA[C/T]GGCCAGAAGATGGGA | 51429 |
| rs75855419 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157786499 | AGTGGAATGGTTCCT[A/G]TTTGTAGATAACAGA | 51429 |
| rs75885421 | snp | C/G | 0.0707826 | 0.174302 | intron-variant | SNX9 | GRCh38.p7 | 6:157781328 | TGGGTGATGTGACCA[C/G]CTGCTCTGTTAGGAC | 51429 |
| rs75935073 | snp | A/G | 0.12932 | 0.218944 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894413 | CTGTGCCCGGCCCCT[A/G]TATTATTTGTTTTAC | 51429 |
| rs75959852 | snp | C/G | 0.370162 | 0.219229 | intron-variant | SNX9 | GRCh38.p7 | 6:157900475 | CCAGGCGGATCGGCC[C/G]GTTGAGAAATAATAG | 51429 |
| rs75962148 | snp | C/G | 0.112631 | 0.208878 | intron-variant | SNX9 | GRCh38.p7 | 6:157939873 | CGCTGGCTTTCTCAG[C/G]CTGGAGGGTTTGGGA | 51429 |
| rs75993332 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | SNX9 | GRCh38.p7 | 6:157841908 | GACAAAAGTAGAACA[A/G]CACAGTGACACTCCC | 51429 |
| rs75997544 | in-del | CTCCTCCACTCCTCCAC/TCCCCCACCTCCTCCA | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157774239 | CCTCCACTCCCCCAC[lengthTooLong]CTCCTCCACCTCCTC | 51429 |
| rs75997988 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157795798 | ACATTTGGGCAAAGG[G/T]AACAGTCTTCCCAAT | 51429 |
| rs76037039 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | SNX9 | GRCh38.p7 | 6:157744248 | GTTGTAGAGCAGGGA[C/T]GAGACCACCCATCTT | 51429 |
| rs76055557 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157816305 | TTCTAAAGAGTATAA[C/G]AATAAACTTGTTACC | 51429 |
| rs76068354 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SNX9 | GRCh38.p7 | 6:157906025 | GTTCTAGTGCACCCG[A/G]AAGACAGGACAAGGT | 51429 |
| rs76083297 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | SNX9 | GRCh38.p7 | 6:157754257 | GTCTGCTTTGGCAAA[C/G]AGCTATTAGTGTCTT | 51429 |
| rs76132646 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | SNX9 | GRCh38.p7 | 6:157908886 | CAGATAGAAGAGAAG[A/G]CCAGTGAGAAAAGAA | 51429 |
| rs76133077 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157935304 | AAAAGATCCAGACAA[C/T]GGTCATTCTAGGTAA | 51429 |
| rs76160215 | snp | A/G | 0.0452528 | 0.143452 | downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157945414 | TTGCCCTACTTACAA[A/G]CAAGTAATTTAGTCT | 51429 |
| rs76206179 | snp | C/T | 0.108755 | 0.206276 | intron-variant | SNX9 | GRCh38.p7 | 6:157748179 | TTCATTTTGTTTTTA[C/T]AGCATTTGTAGATTT | 51429 |
| rs76211234 | snp | A/T | 0.0327778 | 0.123752 | intron-variant | SNX9 | GRCh38.p7 | 6:157919620 | TGTCATATTTTTCTT[A/T]AATTTTTTAGGCTTC | 51429 |
| rs76235058 | snp | A/C/T | 0.0279526 | 0.114869 | intron-variant | SNX9 | GRCh38.p7 | 6:157916460 | AGGACTTCCTGTATG[A/C/T]TCTTGAGTAGAAATA | 51429 |
| rs76255456 | snp | A/G | 0.208779 | 0.246578 | intron-variant | SNX9 | GRCh38.p7 | 6:157782364 | ATTTCCAGAGCCCCA[A/G]ATAGGGAACCTAGGA | 51429 |
| rs76281248 | snp | A/C | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157897353 | CAAATAAAGAGCCAG[A/C]TGAAGAGATGCATAG | 51429 |
| rs76283261 | snp | A/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157825275 | ACGAGACTCCGTTTG[A/G]AAAAAGAGAAGACGG | 51429 |
| rs76296597 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, downstream-variant-500B | SNX9, LOC107986663 | GRCh38.p7 | 6:157715059 | TAAAAAAAAAAAAAA[A/G]AAGAAGAAGAAGCAG | 51429 |
| rs76304147 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157769316 | CATCGATCCGACCAA[A/C]AATCAACAAATTTTT | 51429 |
| rs76316210 | snp | C/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157786045 | TCCACAATAAAATCC[C/T]TGTTTTTTTAAGAGA | 51429 |
| rs76342058 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | SNX9 | GRCh38.p7 | 6:157903713 | GTCTCTGACTCTGGT[C/T]TTTGGTGCTCTCCTC | 51429 |
| rs76347872 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157926946 | CCTGAGATTACATTC[A/G]GAGTATAAAGGTATT | 51429 |
| rs76348800 | snp | A/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157803041 | GTAGTTTCTGACTCA[A/G]CTCAATTAGAAGGCC | 51429 |
| rs76365998 | snp | C/G | 0.103438 | 0.202533 | intron-variant | SNX9 | GRCh38.p7 | 6:157908937 | GCAAGCCTTGCCCAG[C/G]TGGACGTGATACCCG | 51429 |
| rs76369705 | snp | A/G | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157733481 | CAAGACTCTATCTCA[A/G]AAAAAAAAAAAATGA | 51429 |
| rs76429507 | snp | A/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157895626 | TTATGCTGTTAAGAG[A/G]AAAAAAAAAAGTACC | 51429 |
| rs76443121 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | SNX9 | GRCh38.p7 | 6:157732710 | GTGGATGTTTTGTTT[G/T]GTTTTGTTTTGTTTG | 51429 |
| rs76444485 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157773527 | TGAGAAGCCATGGAA[C/T]GGTTTAAAGGGCAGC | 51429 |
| rs76447003 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157880521 | AAATTCATCTTCAAC[C/T]GAATCACTTATTTCC | 51429 |
| rs76468430 | snp | G/T | 0.0479149 | 0.147179 | intron-variant | SNX9 | GRCh38.p7 | 6:157901268 | CAATAGTTTCAGGGG[G/T]TCTCCCTACACCAGC | 51429 |
| rs76469284 | snp | G/T | 0.131381 | 0.220067 | intron-variant | SNX9 | GRCh38.p7 | 6:157769241 | GGCACTGCATTTCCC[G/T]CATTGCTAAGTGACA | 51429 |
| rs76499900 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SNX9 | GRCh38.p7 | 6:157852760 | TTTTGTATTTGTAGA[A/G]ACAGGGTCTCTCCAC | 51429 |
| rs76502607 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | SNX9 | GRCh38.p7 | 6:157859457 | TAATATTCCATTTTG[A/G]CAGCATAGCCTGGTT | 51429 |
| rs76509191 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | SNX9 | GRCh38.p7 | 6:157824458 | TAGCATCAGCACCCC[A/T]TTGTCTATTTGTTTT | 51429 |
| rs76563883 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157936157 | TCTTCTTTTCTGTTT[C/G]TGTGTATCTTTTTTA | 51429 |
| rs76614164 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | SNX9 | GRCh38.p7 | 6:157841976 | CCGTTTTGTTTCCTC[C/T]AGCCTCCCCTCCCCT | 51429 |
| rs76650258 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | SNX9 | GRCh38.p7 | 6:157729981 | CTGTAGAGATAGACA[G/T]TAGATGAGTTGTTGC | 51429 |
| rs76679703 | snp | A/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157794965 | GGAAGAGCAGAATTT[A/T]AAAAAAAAAAAAAAG | 51429 |
| rs76705444 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | SNX9 | GRCh38.p7 | 6:157717037 | GCTGTGACACCTGAT[C/G]CATCTAGCCAGCGTT | 51429 |
| rs76711670 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SNX9 | GRCh38.p7 | 6:157725706 | AAAGGCATCAACTGA[A/G]TGTCAGAGATTACGG | 51429 |
| rs76717296 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | SNX9 | GRCh38.p7 | 6:157781167 | CACCATTCATGTTTT[C/T]CAAGGTCAAAAAAAA | 51429 |
| rs76729587 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157922755 | TTTGTGAATTTGTGT[A/G]TATCACAGGTCTCCT | 51429 |
| rs76848999 | snp | C/T | 0.0506822 | 0.151451 | intron-variant | SNX9 | GRCh38.p7 | 6:157931244 | GGCAAAACTGAGGTA[C/T]CACAGGGGTACAATT | 51429 |
| rs76864309 | snp | C/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157758113 | GAGTTCAAAGTTACA[C/G]TGAGGTGTGATCTCA | 51429 |
| rs76875779 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | SNX9 | GRCh38.p7 | 6:157742753 | TTTTTCTACAATGCA[A/G]TAATCACATTTGTAA | 51429 |
| rs76956823 | in-del | -/CTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157927718 | GTTTTTAATTTTAAG[-/CTT]TTTTTTTTTTTTTTT | 51429 |
| rs76959979 | snp | A/G | 0.127599 | 0.217986 | intron-variant | SNX9 | GRCh38.p7 | 6:157766330 | GGAATATAAAATGGA[A/G]CAAAGAAATCTTTCC | 51429 |
| rs77012949 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | SNX9 | GRCh38.p7 | 6:157935311 | CCAGACAATGGTCAT[C/T]CTAGGTAACGATCAT | 51429 |
| rs77040881 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | SNX9 | GRCh38.p7 | 6:157728307 | CACTCAAAACCCAAA[A/G]GACAGGGTCAACTTC | 51429 |
| rs77052819 | snp | C/T | 0.030665 | 0.119967 | intron-variant | SNX9 | GRCh38.p7 | 6:157860227 | AACATAGTGAGATCT[C/T]GTCTCTTTAAAAAAA | 51429 |
| rs77065099 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157881989 | TTTCAGAGCAGATGA[A/C]ACAGCCTTCTATTAT | 51429 |
| rs77067742 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157920924 | TCCATTATTGCATTA[A/G]TGGAAAAATTCCTTT | 51429 |
| rs77099533 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | SNX9 | GRCh38.p7 | 6:157830204 | TTACATTTCAGTCTT[G/T]TCTTGAGATAATTTC | 51429 |
| rs77148346 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SNX9 | GRCh38.p7 | 6:157865429 | AACACCTCAGCATGG[C/T]TGCTTTGTTCTTCAT | 51429 |
| rs77162126 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157851117 | AAAAAAATTAGTGGG[A/G]CATGGTGGCACATGC | 51429 |
| rs77181930 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157872637 | CATTAATTCGTATAG[C/T]GACTTGGGTGCCAGA | 51429 |
| rs77183395 | snp | A/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157902903 | AAGCTCCTGGTCTCA[A/G]GTGATCCGCCCGCCT | 51429 |
| rs77192870 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157732403 | TGACCCCTAATTTAT[A/T]TCCTCATCTTTATTA | 51429 |
| rs77279689 | snp | A/G | 0.0279526 | 0.114869 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893366 | ATAACAAGTAACTTC[A/G]GTTTTTTCCTTAGAG | 51429 |
| rs77284805 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | SNX9 | GRCh38.p7 | 6:157769424 | AGAGCACGCTGGGGC[A/G]TGGGCAGCCAGGGGA | 51429 |
| rs77303032 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | SNX9 | GRCh38.p7 | 6:157756886 | TGCCAACCTGCGGCC[A/G]AGGGCCAGATCGCAA | 51429 |
| rs77329554 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157927864 | CTCGAGTAGCTGGGA[C/T]TACATAATTTTAAGC | 51429 |
| rs77352970 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | SNX9 | GRCh38.p7 | 6:157917965 | CCTCCAGTTTTATTA[C/T]GTTCAGAGAACATAC | 51429 |
| rs77380715 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | SNX9 | GRCh38.p7 | 6:157761132 | TAGGAAGAAAAACAC[C/T]GCAGTGGTCTGCTTT | 51429 |
| rs77386683 | snp | A/C | 0.0463947 | 0.145069 | intron-variant | SNX9 | GRCh38.p7 | 6:157915989 | ACTCACTCAATAGTT[A/C]CAGGAGCTTTTTTGT | 51429 |
| rs77399512 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | SNX9 | GRCh38.p7 | 6:157740796 | CAGTGACCTGGCAGA[C/T]AGGAGGCATCTGTGG | 51429 |
| rs77400725 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157852589 | CTACTTTTTTGTTTT[G/T]TTTTTTTGAGACAGG | 51429 |
| rs77404238 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SNX9 | GRCh38.p7 | 6:157810989 | GTGGGAGAATCACTC[A/G]AGCCCAGGAATTCGA | 51429 |
| rs77406838 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157824057 | TTGTGAATGGCATTG[C/T]CGGCATGAATAAAAT | 51429 |
| rs77418190 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | SNX9 | GRCh38.p7 | 6:157898319 | CAAACGCTGGGTTGG[C/T]AAAGTAAAAGCAGAA | 51429 |
| rs77456206 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157732404 | GACCCCTAATTTATT[A/T]CCTCATCTTTATTAA | 51429 |
| rs77495024 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SNX9 | GRCh38.p7 | 6:157831703 | CCTTTGTGGCCTCTC[C/T]GGAGCCTTTCCTTTT | 51429 |
| rs77496279 | snp | C/T | 0.230603 | 0.249246 | intron-variant | SNX9 | GRCh38.p7 | 6:157789444 | AGCAGCCATAGACAA[C/T]CCATGAATGAATGTG | 51429 |
| rs77517242 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157939085 | ACCTGCGTGCCTTGG[A/G]ATCATGGAATGTGAA | 51429 |
| rs77518338 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | SNX9 | GRCh38.p7 | 6:157903221 | CAATTCCATGATTCA[A/G]GGCAGATATCAAAGA | 51429 |
| rs77519573 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157749017 | TGAGGAAGTAGGTAG[C/T]GGAAAATCTCTGTCA | 51429 |
| rs77523326 | snp | A/G | 0.039522 | 0.134904 | intron-variant | SNX9 | GRCh38.p7 | 6:157817011 | AAAAGAGATCCCACC[A/G]CGCTTGTTCACCCTT | 51429 |
| rs77533558 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | SNX9 | GRCh38.p7 | 6:157752522 | GTTAAGAAAAAGTGC[C/T]GGGCTTTGATGTGCA | 51429 |
| rs77559877 | snp | A/C | 0.370162 | 0.219229 | intron-variant | SNX9 | GRCh38.p7 | 6:157900474 | CCCAGGCGGATCGGC[A/C]CGTTGAGAAATAATA | 51429 |
| rs77597026 | snp | A/C | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157854999 | AAAAGGGCAAAAAAA[A/C]CCCACTGAAAATTCC | 51429 |
| rs77597432 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157828375 | TATAGTTTTACTTTA[A/G]TTGTCCACTTAAAAC | 51429 |
| rs77609886 | snp | A/C | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157864743 | ATGTGTTTTTAAAAA[A/C]CACCAGCCGGGCATG | 51429 |
| rs77631178 | snp | A/T | 0.0744748 | 0.178019 | intron-variant | SNX9 | GRCh38.p7 | 6:157811459 | TATTCAATATATTAT[A/T]GTTGCTTAAAAAATA | 51429 |
| rs77651754 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157829017 | GTGAGATAAGTGACT[C/T]GATTATTGAAGTAGA | 51429 |
| rs77666965 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SNX9 | GRCh38.p7 | 6:157828809 | GTCTAAGCATCACTT[C/T]CCCGGGAAAGCCTTT | 51429 |
| rs77783612 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | SNX9 | GRCh38.p7 | 6:157719672 | GAGAGACACACACAC[C/T]GTAGCTCAGTGATGC | 51429 |
| rs77783968 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157791775 | TTTTTCTCTTACGCC[C/T]TTCTCAGCTTGGATT | 51429 |
| rs77815825 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | SNX9 | GRCh38.p7 | 6:157929869 | CTATTCAATCCAGAT[A/C]TGAAAATCCAAAGCC | 51429 |
| rs77821403 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157845007 | AGCAAGATGGAGTCA[A/G]TTAAGTTAGATCTCC | 51429 |
| rs77836866 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SNX9 | GRCh38.p7 | 6:157768673 | ATCAAAGTACCATAC[A/G]CATATTGTTGCAAAC | 51429 |
| rs77845157 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | SNX9 | GRCh38.p7 | 6:157903304 | GACATCAAGATCTAG[A/G]TCTAGATCTAGTTTA | 51429 |
| rs77854895 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157798173 | AGTGATCAAAGTTAA[C/T]ATCATCTGTAATGAA | 51429 |
| rs77907712 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | SNX9 | GRCh38.p7 | 6:157800616 | GGAGCTGTGACTGCA[C/T]CACTGCACTCCAGCC | 51429 |
| rs77910651 | snp | G/T | 0.0429648 | 0.14013 | intron-variant | SNX9 | GRCh38.p7 | 6:157877917 | TTCCTGAGTGTCGTA[G/T]TTTTCTTTAAGTATA | 51429 |
| rs77963086 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | SNX9 | GRCh38.p7 | 6:157742067 | AACACTATTTATTTC[C/T]TCTCTCCAGCCTCTT | 51429 |
| rs77971215 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | SNX9 | GRCh38.p7 | 6:157748340 | CTTTAAAATGGGTCT[A/G]TACCTTGTTTTACAA | 51429 |
| rs77986047 | snp | A/C | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157743413 | AGCCTGAGGCCTATG[A/C]AAAAAAAAAAAAACA | 51429 |
| rs78004726 | snp | C/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157827863 | AGGAGTTCCTGATGC[C/T]TTTTTTTTTTTTTTA | 51429 |
| rs78011787 | snp | A/T | 0.133093 | 0.220981 | intron-variant | SNX9 | GRCh38.p7 | 6:157940010 | ATGTATTCAGCAAAC[A/T]TGAAGAAAGTTGTCC | 51429 |
| rs78091021 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | SNX9 | GRCh38.p7 | 6:157935428 | AACACAGGGACAGGG[C/G]AGTGTGTGACATATC | 51429 |
| rs78099786 | snp | G/T | 0.227369 | 0.248974 | intron-variant | SNX9 | GRCh38.p7 | 6:157792146 | CCTGCCTTCCTTCCT[G/T]CCTTCTTTTTTTTTT | 51429 |
| rs78130497 | snp | A/G | 0.046775 | 0.145601 | intron-variant | SNX9 | GRCh38.p7 | 6:157864379 | TTTTGGAGGGTCCAA[A/G]CCCTCTAACCTTAGC | 51429 |
| rs78181738 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | SNX9 | GRCh38.p7 | 6:157716836 | TAGAAATTTGTCTCA[C/T]GTTGCCCATAAGTGA | 51429 |
| rs78230639 | snp | G/T | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157730657 | TTTTTTTTTTTTTTT[G/T]GGGTCGGAGTCTTGC | 51429 |
| rs78245188 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | SNX9 | GRCh38.p7 | 6:157791520 | TTGAATAAATAAATG[A/T]GAATCATGATTTTGC | 51429 |
| rs78271553 | snp | C/T | 0.0279526 | 0.114869 | intron-variant, upstream-variant-2KB, nc-transcript-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157893029 | CCAATGATAGTCTGT[C/T]CCTAGTGTCCCAAAC | 51429 |
| rs78272219 | snp | A/G | 0.0748431 | 0.178382 | intron-variant | SNX9 | GRCh38.p7 | 6:157848562 | TTTTTTATTTAAAAG[A/G]AACTGTACTTTCTGT | 51429 |
| rs78280543 | snp | A/C/G | 0.00636936 | 0.0560724 | intron-variant | SNX9 | GRCh38.p7 | 6:157734706 | TACTCTTGAACAAAG[A/C/G]CCTCTCCAGCGTTAT | 51429 |
| rs78289055 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157743197 | TTAGTTAAATCCTCA[C/T]TAATGTTAACTTTGA | 51429 |
| rs78301134 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | SNX9 | GRCh38.p7 | 6:157925599 | AAATTGGGGATTACT[C/T]ATAAAGTAGAATATT | 51429 |
| rs78301969 | snp | C/G | 0.0807149 | 0.183963 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893299 | GTGTTTGAGAAGTCA[C/G]AGTCTTGTGGATGAA | 51429 |
| rs78316961 | snp | C/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157927722 | TTAATTTTAAGCTTT[C/T]TTTTTTTTTTTTTTT | 51429 |
| rs78319698 | snp | A/G | 0.122411 | 0.214991 | intron-variant | SNX9 | GRCh38.p7 | 6:157856641 | TCTCTTCATTTATAG[A/G]TTCCCTTACCTCACT | 51429 |
| rs78323152 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157813017 | GATTAGCTATGTTTA[A/T]GAAATTGAAGATAAA | 51429 |
| rs78359392 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | SNX9 | GRCh38.p7 | 6:157911415 | CACTGCACTCGCAAG[A/G]GTCGAGAGAAACAGT | 51429 |
| rs78370473 | snp | A/C | 0.0410537 | 0.137264 | intron-variant | SNX9 | GRCh38.p7 | 6:157800377 | GAGTGCAGTGGCTCA[A/C]ACCTGTAATCCCAAC | 51429 |
| rs78463370 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | SNX9 | GRCh38.p7 | 6:157799987 | ATGAGGGGGAAAACT[C/T]TTCCTAAATATCTCC | 51429 |
| rs78503206 | snp | C/T | 0.106278 | 0.204558 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890467 | CTTTTAAATTTAGAA[C/T]GTTAAACCAGCAAAT | 51429 |
| rs78590832 | snp | C/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157901871 | TTTTTTTTTTTTTAA[C/T]TGATGATCTTCCATT | 51429 |
| rs78605186 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885500 | TCAGTCCCTTTTGAG[A/G]AAAAGAGTTAAATTT | 51429 |
| rs78608923 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | SNX9 | GRCh38.p7 | 6:157756855 | AAACTGGGCATCTCA[A/G]CAACAAAGCAGGCTG | 51429 |
| rs78646917 | snp | G/T | 0.0283406 | 0.115616 | intron-variant | SNX9 | GRCh38.p7 | 6:157847233 | TCAGCCTCCAAGTTA[G/T]CTGAGACCACAGGTG | 51429 |
| rs78680847 | snp | A/C | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157901870 | TTTTTTTTTTTTTTA[A/C]CTGATGATCTTCCAT | 51429 |
| rs78681857 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | SNX9 | GRCh38.p7 | 6:157803105 | ACTAACTTGTCTTTC[A/G]TGTGTGCATGTAGCA | 51429 |
| rs78703890 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | SNX9 | GRCh38.p7 | 6:157903672 | TTTTCATGGCTGATG[A/C]GTGAGGTTCCAGCTC | 51429 |
| rs78706103 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | SNX9 | GRCh38.p7 | 6:157942595 | CACCAGGGCCAGCTC[A/G]GGCCCCAGCGCTGCC | 51429 |
| rs78732418 | snp | C/G | 0.0356815 | 0.128715 | intron-variant | SNX9 | GRCh38.p7 | 6:157903896 | CAGTCCTAACTTGAA[C/G]CTGTGCCTCTGAGGC | 51429 |
| rs78736453 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157900248 | TTCATATACCTCTTG[A/G]CCATTTTTTGGTCTT | 51429 |
| rs78738215 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | SNX9 | GRCh38.p7 | 6:157860066 | TGCGGCAGCAGAGAC[A/G]GACTGAATGGCCTGC | 51429 |
| rs78742924 | snp | C/T | 0.118584 | 0.212673 | intron-variant, nc-transcript-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885343 | GTGGTTTTCTAACGT[C/T]AGTACAGATTCATCT | 51429 |
| rs78764391 | snp | A/G | 0.0558544 | 0.157504 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157892573 | ACATAACCAACTAGT[A/G]TGACAGTTACTACAC | 51429 |
| rs78819391 | snp | A/T | 0.5 | 0 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886296 | GCAAGAATACAACAT[A/T]AAAAAAAAATAACAA | 51429 |
| rs78839977 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SNX9 | GRCh38.p7 | 6:157898769 | ACATTGGGCCAAGAA[C/T]TGAATGTCTGTTCTA | 51429 |
| rs78858180 | snp | A/C | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157743414 | GCCTGAGGCCTATGC[A/C]AAAAAAAAAAAACAA | 51429 |
| rs78865169 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | SNX9 | GRCh38.p7 | 6:157915231 | AATCAAGTAGCGTGA[A/G]TCCTCCAACTTGGTT | 51429 |
| rs78868861 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | SNX9 | GRCh38.p7 | 6:157917608 | TCCAGAACCTCCCAC[A/G]GATACCAAAATCCAT | 51429 |
| rs78899058 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | SNX9 | GRCh38.p7 | 6:157779305 | ATAATGATGCCTTCC[C/T]GAGCCTCCTCATGGT | 51429 |
| rs78941082 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | SNX9 | GRCh38.p7 | 6:157755616 | CACTGATTTAAGCTT[A/G]AATGTGAGAGATTTA | 51429 |
| rs78947320 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SNX9 | GRCh38.p7 | 6:157869848 | CTCACATTATGCATA[C/T]CCCCACACACACTCG | 51429 |
| rs78947945 | in-del | -/C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157721655 | TCTCTCCTCTGACCT[-/C/T]CCCGTCCACTCCTCC | 51429 |
| rs78968069 | snp | G/T | 0.0279526 | 0.114869 | intron-variant | SNX9 | GRCh38.p7 | 6:157917433 | TTAAATGCTAAAAAC[G/T]TTCCTCTAAGCATGC | 51429 |
| rs79001053 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | SNX9 | GRCh38.p7 | 6:157764351 | GCAGTAACCAGCAAA[C/T]AGACCTTCTCCCAAT | 51429 |
| rs79007253 | snp | G/T | 0.0341408 | 0.126114 | intron-variant | SNX9 | GRCh38.p7 | 6:157788602 | TAAATATTATAGGGT[G/T]GTGGAATCATCCCTT | 51429 |
| rs79032438 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SNX9 | GRCh38.p7 | 6:157807900 | TTCCAAACCTGCATT[A/G]TGCAGAGGTGTGGAG | 51429 |
| rs79033115 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | SNX9 | GRCh38.p7 | 6:157790857 | TCTTTCTGGTTCTCT[A/G]TTCTCTCCCTAAGTA | 51429 |
| rs79037058 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157859939 | TTATAGGAGTCAGCA[A/G]ATTTTGGCCCATGAA | 51429 |
| rs79057103 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | SNX9 | GRCh38.p7 | 6:157804878 | CTTTACTGCGGTAGG[G/T]AGGAGCAGTGCTCGG | 51429 |
| rs79062502 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | SNX9 | GRCh38.p7 | 6:157763134 | AGTGAGGGAAGTCAC[A/G]CCCAGAGGGTGCTGA | 51429 |
| rs79084332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157868554 | TTAGAGGCAAACATA[A/G]TATTCATTTGTGTCC | 51429 |
| rs79109086 | snp | C/T | 0.0584853 | 0.160693 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157944138 | GCCACCGTCTCACCC[C/T]TGCGGAGGAGCGCTC | 51429 |
| rs79138110 | snp | A/T | 0.04875 | 0.148319 | intron-variant | SNX9 | GRCh38.p7 | 6:157917498 | TTTTCATGTTCATTC[A/T]GGTCAAAACATTTTC | 51429 |
| rs79145822 | snp | C/T | 0.140581 | 0.224783 | intron-variant | SNX9 | GRCh38.p7 | 6:157813912 | TCTCTCCTGATTTTT[C/T]AGAAGGTCAGATAAA | 51429 |
| rs79171131 | snp | A/C | 0.0618563 | 0.164627 | intron-variant | SNX9 | GRCh38.p7 | 6:157843087 | TTCTTTCAGTGTCAT[A/C]ATTTCCTCAATTATA | 51429 |
| rs79173237 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SNX9 | GRCh38.p7 | 6:157799886 | TGGAGACATAGTCAA[A/G]CCATATCACTGCTAT | 51429 |
| rs79191237 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | SNX9 | GRCh38.p7 | 6:157741925 | CACCTGGCCCCATCA[C/T]TCTGTCAATTCAACA | 51429 |
| rs79210569 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | SNX9 | GRCh38.p7 | 6:157761375 | CAGACAACAACATGT[A/G]TCAAGCGGTCTATGA | 51429 |
| rs79243870 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | SNX9 | GRCh38.p7 | 6:157726377 | AACTATTTGAACATA[C/T]AGAATACAGGTATTG | 51429 |
| rs79271980 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | SNX9 | GRCh38.p7 | 6:157767534 | CGAACCTTCCATGTG[A/T]TTTTCCTCAATCAGC | 51429 |
| rs79353388 | snp | G/T | 0.0279526 | 0.114869 | intron-variant | SNX9 | GRCh38.p7 | 6:157916023 | TATGGATTCTTTGGT[G/T]TTTTTGTCTTTTCTT | 51429 |
| rs79377442 | snp | G/T | 0.0592355 | 0.161582 | intron-variant | SNX9 | GRCh38.p7 | 6:157864139 | TGCTGGCAGGGTAGG[G/T]CCCGGCTCTGCTTCC | 51429 |
| rs79453126 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | SNX9 | GRCh38.p7 | 6:157773045 | GGGAAAGTGATGATG[C/T]CGTCACTAAGGCAAT | 51429 |
| rs79488806 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157772476 | AGTGAAAAGGGAGGC[A/G]GAGAGTGGGGTGATG | 51429 |
| rs79490820 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | SNX9 | GRCh38.p7 | 6:157799841 | AACACTGGGGAATTC[C/T]GGGAGATCCAATTCA | 51429 |
| rs79503308 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SNX9 | GRCh38.p7 | 6:157865619 | CAGACATGGAGAAAG[A/G]TTGGAATTGAATACC | 51429 |
| rs79529229 | snp | A/G | 0.226484 | 0.248892 | intron-variant | SNX9 | GRCh38.p7 | 6:157792024 | TTGTTTTGGATTTCC[A/G]TGGGATCCAGTCCTT | 51429 |
| rs79541186 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157742113 | TAGCACTGCTAACTC[A/G]GAAATCTCTGCTGCT | 51429 |
| rs79574675 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | SNX9 | GRCh38.p7 | 6:157839798 | CCTTTCCTCCTGCCC[C/T]TCAGTTTAGTAACTC | 51429 |
| rs79597339 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | SNX9 | GRCh38.p7 | 6:157839930 | GTCTTAATGTGATAC[A/G]TAGCTGTTTGGATTC | 51429 |
| rs79606212 | snp | C/T | 0.106987 | 0.205054 | intron-variant | SNX9 | GRCh38.p7 | 6:157729526 | GTAGGCAGCAGAGAG[C/T]GCTGACATATATAAT | 51429 |
| rs79607439 | snp | C/T | 0.0452528 | 0.143452 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157892467 | ACAAGATAAAGAGAG[C/T]GTTCCAGGAAAAAAA | 51429 |
| rs79613221 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | SNX9 | GRCh38.p7 | 6:157863558 | GGAAATTTAGCTCTT[A/C]GAAATAGTTGAAGAA | 51429 |
| rs79656564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157833167 | TGAAAATTTAGACGT[A/G]TGTATAAATAGTTGC | 51429 |
| rs79683938 | snp | C/G/T | 0.0123036 | 0.0774623 | intron-variant | SNX9 | GRCh38.p7 | 6:157933863 | CTGTGATTATCAATA[C/G/T]ATAATTAAATGTTCC | 51429 |
| rs79735483 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157928906 | AGCCAGGTTAAGAAA[G/T]CTCATAGGGAACACC | 51429 |
| rs79738841 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | SNX9 | GRCh38.p7 | 6:157876745 | GGGGTTCTCAACCTG[A/C]GCCTCATTGCCGTTT | 51429 |
| rs79739234 | snp | A/T | 0.0402882 | 0.136092 | intron-variant | SNX9 | GRCh38.p7 | 6:157747904 | GATGTTACCAATGTT[A/T]ATCTTTACTAGGGCT | 51429 |
| rs79746993 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | SNX9 | GRCh38.p7 | 6:157939152 | GTGTCAAGAAAAAAA[A/G]AAGATGAATTTCTAT | 51429 |
| rs79761590 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SNX9 | GRCh38.p7 | 6:157799984 | TTCATGAGGGGGAAA[A/G]CTTTTCCTAAATATC | 51429 |
| rs79772644 | snp | A/C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157747581 | TATTAACTACTCGTT[A/C/T]GAGGCATATTGCAAT | 51429 |
| rs79833289 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157746591 | TGGAGAGCAACCAGA[A/C]ACCCTCCCATCCTTA | 51429 |
| rs79932478 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | SNX9 | GRCh38.p7 | 6:157750509 | AATGTAAAACCCAAA[A/G]CTGTAAAACTCCTAG | 51429 |
| rs79939508 | snp | G/T | 0 | 0 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157891050 | TTTTTTTTTTTTTTT[G/T]AGACAGAGTCTCACT | 51429 |
| rs79951429 | snp | C/T | 0.0766824 | 0.180169 | intron-variant | SNX9 | GRCh38.p7 | 6:157790159 | CATGGCCACAGGGAG[C/T]GCAAGGGGAACTGGG | 51429 |
| rs79960023 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | SNX9 | GRCh38.p7 | 6:157853969 | GACTGGTGAAACAGT[A/G]GTGTGAGGATTTGAA | 51429 |
| rs79961759 | snp | C/G | 0.145305 | 0.227022 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822794 | CGGGGCTCCTGTCTG[C/G]CCGGGGCGTCGAGAG | 51429 |
| rs79982854 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | SNX9 | GRCh38.p7 | 6:157747305 | TACATGCACACACAA[A/G]CACACAAGATATTTT | 51429 |
| rs80000117 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SNX9 | GRCh38.p7 | 6:157830919 | ATTCTGGATGATTTC[A/G]TTTGTTCTTACCTTC | 51429 |
| rs80002520 | snp | A/T | 0.0298908 | 0.118541 | intron-variant | SNX9 | GRCh38.p7 | 6:157857460 | GTGATTACCTTTTTT[A/T]AAAAAAAATTAATCT | 51429 |
| rs80009347 | snp | A/G | 0.0744748 | 0.178019 | intron-variant | SNX9 | GRCh38.p7 | 6:157788166 | TGTTAGTAATAACAG[A/G]GAGAAGATACTAGAG | 51429 |
| rs80009789 | snp | G/T | 0.0245949 | 0.108132 | intron-variant | SNX9 | GRCh38.p7 | 6:157906095 | CTTACAAGGAAAGTC[G/T]TAAGACTGATGAACA | 51429 |
| rs80011087 | snp | C/G/T | 0.0349115 | 0.127424 | intron-variant | SNX9 | GRCh38.p7 | 6:157774540 | GCGGTCATCGACCCA[C/G/T]GTGTCTGCCTTAGGA | 51429 |
| rs80016278 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | SNX9 | GRCh38.p7 | 6:157851459 | TTTTTTCACCATCCC[A/G]AATAGAAACTCTGTA | 51429 |
| rs80025060 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SNX9 | GRCh38.p7 | 6:157741290 | GAGGTGGAGCTGCAA[C/T]GAGCCGAGATTGTGC | 51429 |
| rs80080564 | snp | G/T | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157730660 | TTTTTTTTTTTTTGG[G/T]TCGGAGTCTTGCTTT | 51429 |
| rs80088133 | snp | A/C | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157796003 | TAAAGAGGAAGTGTG[A/C]CTTGACGAATTGGCA | 51429 |
| rs80123938 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | SNX9 | GRCh38.p7 | 6:157866817 | TCTTAGATGTGTGTG[C/T]GTGTGTGTATGTCTC | 51429 |
| rs80135770 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157792036 | TCCGTGGGATCCAGT[A/C]CTTTTGAATTCAGTT | 51429 |
| rs80146614 | snp | C/T | 0.231189 | 0.249291 | intron-variant | SNX9 | GRCh38.p7 | 6:157790419 | GATTTCCTCAAGATT[C/T]TGTTCATTTGTGGCC | 51429 |
| rs80153909 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | SNX9 | GRCh38.p7 | 6:157796135 | TTAAGTGATCTTTTT[C/T]TTTTCTTAATTATTG | 51429 |
| rs80183373 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887606 | CTCTGTCTGTCTCCC[A/G]TATCTCAGGATCACT | 51429 |
| rs80191721 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | SNX9 | GRCh38.p7 | 6:157934985 | AAAGAAAATGTGAGC[A/G]TTAGTGAAAATAATA | 51429 |
| rs80196387 | snp | C/G | 0.0356815 | 0.128715 | intron-variant | SNX9 | GRCh38.p7 | 6:157907952 | TCTTGGATCTGGGCT[C/G]TCCCTGAGGGGGTTA | 51429 |
| rs80223676 | snp | A/T | 0.0418186 | 0.138422 | intron-variant | SNX9 | GRCh38.p7 | 6:157767633 | TTTATTTGGGTTTTT[A/T]AGGAACTGAAATTTG | 51429 |
| rs80258061 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SNX9 | GRCh38.p7 | 6:157920606 | GCATAAACACTTCTC[A/G]GGTGGCCATTCGCCT | 51429 |
| rs80288343 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157730570 | ATAAGTGAAATRAAA[-/A]AWGAAAACCATCCAT | 51429 |
| rs80330855 | snp | C/T | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157914471 | TCATTTTCTTTTTCT[C/T]TTTTTTTTTTTTTTT | 51429 |
| rs111218826 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157827169 | TATAGTTTATATAAT[A/C]TATAAACATATATTA | 51429 |
| rs111231147 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157805664 | AAGTTTAAATAAATC[A/G]ACCTTTCCCACCTGA | 51429 |
| rs111244883 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SNX9 | GRCh38.p7 | 6:157851942 | AATGTTTTCAAGGTT[C/T]GTCTGTAATGTAGCA | 51429 |
| rs111247706 | in-del | -/GTT | 0.375 | 0.216506 | intron-variant | SNX9 | GRCh38.p7 | 6:157937066 | TTAAAATGATTAGTT[-/GTT]TTAATATTTTTATAT | 51429 |
| rs111281601 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | SNX9 | GRCh38.p7 | 6:157912636 | GTAAGAATTCCCCTC[G/T]CGCTCAACTACTGGA | 51429 |
| rs111284685 | snp | A/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157922233 | AACGTTGGCTGCCTG[A/T]CATCTCAAAAGTGTC | 51429 |
| rs111288922 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | SNX9 | GRCh38.p7 | 6:157743472 | TGGAGACATCAAAGA[A/C]CCAGTGTGTAATCAA | 51429 |
| rs111301365 | snp | C/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157914441 | AATAACTTGTCGCAG[C/T]TGTGGCTTGGCTTGT | 51429 |
| rs111342149 | in-del | -/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157838112 | CAATTTCCCGGGCTC[-/G]AACAATCTTTCCACC | 51429 |
| rs111350360 | snp | A/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157776856 | AGGTATGATATTTAC[A/G]GGCTATGTGCCTGAG | 51429 |
| rs111353957 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | SNX9 | GRCh38.p7 | 6:157779187 | CAACAAGGACAAGGG[A/G]AAGAGCCAGCAGATG | 51429 |
| rs111378118 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157827536 | TTTATATAATATATA[A/C]ACATATATTATATTA | 51429 |
| rs111384709 | snp | C/G | 0.384401 | 0.210799 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157823148 | CAGGGCGCGCTTCCG[C/G]CGGGCGTCGCGCGCG | 51429 |
| rs111387776 | snp | A/G | 0.27008 | 0.249192 | intron-variant | SNX9 | GRCh38.p7 | 6:157843911 | ATGGAGTCTCACTCT[A/G]CCACCCAGGCCAGAG | 51429 |
| rs111398590 | snp | A/G | 0.0744748 | 0.178019 | intron-variant | SNX9 | GRCh38.p7 | 6:157835818 | CTGAACTGTGAGTCA[A/G]TTAAACCTCTTTCCT | 51429 |
| rs111401009 | in-del | -/A | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157770800 | GCGAGACTCCTTCTC[-/A]AAAAAAAAAAAAAAA | 51429 |
| rs111412240 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | SNX9 | GRCh38.p7 | 6:157839415 | AGCATATGTATTTTC[A/C]TGTAATGGTGATATA | 51429 |
| rs111414723 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157867310 | CTAAATGCAATGTGG[C/G]CAGCTGCCAGAAACC | 51429 |
| rs111445888 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157771942 | GACCTCAAGTGATCC[A/G]CCTGCTTTGGCCTCC | 51429 |
| rs111467507 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157908858 | CTGAATTTGTGAACT[C/T]TTGCCCTAGTCACAG | 51429 |
| rs111506943 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157774884 | ATTCCCCCTAGTCCC[A/G]TGAATGCAAGGCCAG | 51429 |
| rs111512053 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157872779 | GGATGCGCATCCCAC[C/T]GCTTCACATTCAGAG | 51429 |
| rs111515039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157936180 | CTTTTTTAATTGTGT[C/T]TAATCATGGTTTCTT | 51429 |
| rs111550703 | snp | A/G | 0.00120229 | 0.0244888 | intron-variant | SNX9 | GRCh38.p7 | 6:157910032 | AAGTCACAGGTGAGT[A/G]TGTGTAATGCTAAAC | 51429 |
| rs111552384 | snp | A/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157928044 | TATGTAATTATAGGA[A/T]AGATTGTTTAAACAA | 51429 |
| rs111559839 | snp | C/T | 0.0505692 | 0.150756 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893478 | CAGCTGTCTGCCCCA[C/T]GTGTCGGTTGGTGAA | 51429 |
| rs111561792 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SNX9 | GRCh38.p7 | 6:157911978 | TCGTGGTGCTGGGGC[A/G]GTGGAGTGACAGCCA | 51429 |
| rs111563502 | snp | C/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157828562 | GCAGTGGCACGAACA[C/G]AGCTCACGGCAGTCT | 51429 |
| rs111584640 | in-del | -/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157816269 | GTCATTTACTTAATA[-/T]TTTTTAAATTAAGCT | 51429 |
| rs111591113 | snp | C/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157772210 | GAAGGAGAGGACAGG[C/G]ATGGGTCAAGGATTT | 51429 |
| rs111592847 | snp | C/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157760806 | TGCACAGACTGACTC[C/T]CTTCCTACTCCCTCA | 51429 |
| rs111622017 | snp | G/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157916346 | GCCCTCTTTTCTTTT[G/T]TAATGTAGACAATCA | 51429 |
| rs111627075 | snp | C/G | 0.0532157 | 0.154195 | intron-variant | SNX9 | GRCh38.p7 | 6:157717008 | GGCTGCATTTTACTG[C/G]CCAAACAGCAATGGC | 51429 |
| rs111632202 | snp | C/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157940578 | ACCTGTTGCCATGCC[C/T]GGCTAATTTTTGTAT | 51429 |
| rs111642138 | snp | A/G | 0.387074 | 0.209071 | intron-variant | SNX9 | GRCh38.p7 | 6:157730839 | GAGATGGGTTTTGCC[A/G]TGTTGGCCAGGCTGG | 51429 |
| rs111653850 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157919784 | CTTGCTATTTCTTTG[C/T]GTATCTCTTAATTTT | 51429 |
| rs111659652 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157944832 | CGGGCTCCTCAGAGC[A/G]TGGTAGCCGACTGTG | 51429 |
| rs111680138 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | SNX9 | GRCh38.p7 | 6:157798228 | GTGAGGGCGCAATGA[C/G]ACGAACTCACCATGA | 51429 |
| rs111701587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157766650 | CTCGGGATGCCAGCT[A/G]ATTGGACAAGCCTTG | 51429 |
| rs111707743 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894323 | CCGTGTTGGCCAGGC[G/T]GATCTCAAACTCCTG | 51429 |
| rs111717409 | snp | G/T | 0.0356815 | 0.128715 | intron-variant | SNX9 | GRCh38.p7 | 6:157907457 | TAGCTAATTTTTTTT[G/T]TATTTTATAGTAGAG | 51429 |
| rs111731514 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157737958 | TTCCATGTAGTTGTG[C/T]GGTTTTGAGTGAGTT | 51429 |
| rs111731871 | snp | C/T | 0.211819 | 0.247067 | intron-variant | SNX9 | GRCh38.p7 | 6:157835045 | TGAGACAGAGTCTTA[C/T]TTTGTCACCCAGGCT | 51429 |
| rs111760241 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | SNX9 | GRCh38.p7 | 6:157905757 | GCCAGCATGTGGCTA[C/T]TGCCCCCTGTGGCCA | 51429 |
| rs111773179 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SNX9 | GRCh38.p7 | 6:157923971 | CCCAGGCTGGGTGTG[A/G]CGGATCACTTGAGGT | 51429 |
| rs111780027 | snp | A/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157934528 | AAAATGGCATTTTAT[A/T]TGCCCCCAGGAGCGG | 51429 |
| rs111789332 | in-del | -/T | 0.415891 | 0.18703 | intron-variant | SNX9 | GRCh38.p7 | 6:157735042 | TTTGGGAGGCCCAGG[-/T]GGGTGGATCACCTGA | 51429 |
| rs111790499 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SNX9 | GRCh38.p7 | 6:157835503 | TTGAAGCCTTGAACT[C/T]CCACACTGAAGCAAT | 51429 |
| rs111794592 | snp | C/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157856508 | AATGCTGCTTTGATC[C/T]CTAAAAAATGAATAC | 51429 |
| rs111807168 | snp | A/T | 0.00134258 | 0.0258745 | intron-variant | SNX9 | GRCh38.p7 | 6:157921494 | AGTCATTCATTTTAG[A/T]CAAAGTTGTATGTCA | 51429 |
| rs111808398 | snp | C/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157871197 | CCAGCCTTAGTAACA[C/T]GGCAAAACCTCATCT | 51429 |
| rs111811577 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157825874 | TTCTTTGTCTTCTTC[A/T]AGGGGTGGGGAGAAT | 51429 |
| rs111811606 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894792 | TTTGACAAAATCCAT[C/T]GGTTCTAAATACACA | 51429 |
| rs111813695 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157744100 | TGAAAATTAAATGAT[A/G]CATTGTATATAAAAC | 51429 |
| rs111813724 | snp | G/T | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157844600 | TTGTTTTTTTTTTTT[G/T]TTTTTTTTTTTGAGA | 51429 |
| rs111819620 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157773296 | CTGCAGCCAGGGTGC[C/T]AGGCCCCAGCTACAC | 51429 |
| rs111832435 | in-del | -/ACTC | 0.0111196 | 0.0737302 | intron-variant | SNX9 | GRCh38.p7 | 6:157799154 | TCAGCTCTCTTGAAA[-/ACTC]ACTCACTATCATGAG | 51429 |
| rs111875645 | snp | C/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157765148 | AGAGACTCCTCTTGC[C/T]TAGACAATGGGCGTT | 51429 |
| rs111882034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157880529 | CTTCAACCGAATCAC[C/T]TATTTCCCCACAAAA | 51429 |
| rs111907241 | snp | G/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157794334 | ACGTGGAACTGTGAG[G/T]CTATTAAACCTCTTT | 51429 |
| rs111948327 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157738044 | GGTTTGCTGAGGAGT[A/G]TTTTACTTCCAATTA | 51429 |
| rs111962660 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | SNX9 | GRCh38.p7 | 6:157837156 | GATCCGTAAAATATT[A/C]TCAGAAGCTATTTAG | 51429 |
| rs111971257 | snp | G/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157825215 | ATCGCGCCACTGCAC[G/T]CCAGCCTGGGCGACA | 51429 |
| rs112003979 | snp | C/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157784369 | TTATCAAAAGGAATT[C/T]TTTTTTTTTTTTTTA | 51429 |
| rs112009677 | snp | A/C | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157777388 | CCATTTAAAAAAAAA[A/C]AAAAAGGCAAAAGCA | 51429 |
| rs112016911 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157879842 | TCTTTAGAGTACTTA[C/T]TTTTGAGAAATTAAT | 51429 |
| rs112019651 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | SNX9 | GRCh38.p7 | 6:157855396 | AAGTCTATTTCTAGA[C/G]GATAAGTTCCTAGAC | 51429 |
| rs112020154 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157917974 | TTATTATGTTCAGAG[A/G]ACATACTTTGCATGA | 51429 |
| rs112034670 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, nc-transcript-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157892930 | GTTAACGGAATTCCA[A/C]CTCACTAGGCTCTTG | 51429 |
| rs112066442 | snp | C/G | 0.0581099 | 0.160244 | intron-variant | SNX9 | GRCh38.p7 | 6:157870949 | ACTCGCATGCTCACA[C/G]AGAGCTCCTGTGGAA | 51429 |
| rs112067655 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, nc-transcript-variant | SNX9, LOC107986663 | GRCh38.p7 | 6:157714120 | TTGCTTATGGAATTC[A/T]GCCCTGGAAGAGATG | 51429 |
| rs112084520 | snp | A/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157896747 | CTCCTGTTGTATTCA[A/G]TTGTGTCAGTTCATT | 51429 |
| rs112096511 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157906596 | ATCAGAATAAGGTAC[C/T]CTTTCAGATATATGG | 51429 |
| rs112110699 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157787750 | TTTGAATTCAAAAAT[A/G]AAGTAGATTTCACTA | 51429 |
| rs112115455 | snp | A/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157934326 | AAGGAGAGAGAGAGA[A/T]GGAAGGTAAACTGAT | 51429 |
| rs112117011 | snp | C/T | 0.444444 | 0.157135 | intron-variant | SNX9 | GRCh38.p7 | 6:157731800 | TACTCTGTCCTGCAT[C/T]AAACTAGGCACTTCC | 51429 |
| rs112136404 | snp | G/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157819714 | CCATACTGAACAAAC[G/T]CAGGGAAGAGGTGGT | 51429 |
| rs112141708 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157870063 | ACGTGTGAGCACGCA[C/G]ACACACCCTCTTCAC | 51429 |
| rs112145320 | in-del | -/TGACCTTTGCTCC/TGGCCTTTGCTCC | 0.243347 | 0.249911 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888059 | CACACCGGGAGACAT[-/TGACCTTTGCTCC/TGGCCTTTGCTCC]TGTGTTCACAGACCA | 51429 |
| rs112150847 | snp | A/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157784258 | GGTTAATCAAATTAA[A/T]AAACCCTAACAAGAC | 51429 |
| rs112166628 | snp | A/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157932106 | ATTTTGAATCACTTC[A/G]AAAGTTACTGTAATC | 51429 |
| rs112167246 | snp | A/G | 0.387074 | 0.209071 | intron-variant | SNX9 | GRCh38.p7 | 6:157730743 | CTTCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 51429 |
| rs112174719 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157804891 | GGGAGGAGCAGTGCT[C/T]GGGGCTCCACCAATA | 51429 |
| rs112184074 | in-del | -/T | 0.26818 | 0.249338 | intron-variant | SNX9 | GRCh38.p7 | 6:157834521 | GGCCAATTTTTTAAA[-/T]TTTTTTTTTCTTTAG | 51429 |
| rs112189436 | snp | C/T | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157738155 | GATGTCTATTAGGTC[C/T]ACTTGGTCCAGAGCT | 51429 |
| rs112215439 | snp | A/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157831364 | CCTTGGAGTCACTAT[A/G]TCTTTAATTCCTGGC | 51429 |
| rs112250281 | snp | A/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157764225 | GGCTCATGGTCATTG[A/G]CGTTCACATTGAAGT | 51429 |
| rs112256082 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | SNX9 | GRCh38.p7 | 6:157939242 | GGTGGATGGCACTTG[C/G]ATGGGCAGAGAATGG | 51429 |
| rs112270152 | in-del | -/A | 0.386884 | 0.209196 | intron-variant | SNX9 | GRCh38.p7 | 6:157730567 | TAGATAAGTGAAATG[-/A]AAAATGAAAACCATC | 51429 |
| rs112283747 | snp | A/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157864987 | GAGCTGAGACTTGCC[A/G]CTGCACTTTAGCCTG | 51429 |
| rs112314744 | snp | A/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157935238 | ATTTCAGCTAATAAA[A/G]AAGGAATGGTAGAAA | 51429 |
| rs112319424 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SNX9 | GRCh38.p7 | 6:157799605 | AGAAAAAGACGTTTA[A/G]TTGGACTTACAGTTC | 51429 |
| rs112335863 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SNX9 | GRCh38.p7 | 6:157942731 | GTTGTGAATAAAGAA[C/T]ACTGTGAGGTCGTAA | 51429 |
| rs112341373 | snp | A/G | 0.17461 | 0.238362 | intron-variant | SNX9 | GRCh38.p7 | 6:157815287 | GCCTGATCTTGGCTC[A/G]CTGCAGCCTCGGATT | 51429 |
| rs112350150 | snp | A/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157728241 | CCCCAAAGAGTTTGA[A/G]GGGAACTCTAGATCT | 51429 |
| rs112353167 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157891085 | CACCCAGGCTGGAGT[A/G]TAGTGGTGTGAACTC | 51429 |
| rs112354431 | in-del | -/CT | 0.0614824 | 0.164198 | intron-variant | SNX9 | GRCh38.p7 | 6:157865906 | GCACTTGCATTAGCC[-/CT]GTTAGACTAGCCCTG | 51429 |
| rs112357598 | snp | C/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157869656 | TGGCCTTGCCTCAAG[C/G]CCAGGGTCTGTCTAA | 51429 |
| rs112370027 | snp | C/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157870065 | GTGTGAGCACGCACA[C/T]ACACCCTCTTCACTC | 51429 |
| rs112371052 | snp | C/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157899210 | AATTACTTCTTCACT[C/G]TCATCTTTTTCTCCC | 51429 |
| rs112372717 | snp | A/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157718240 | AATACTGCTACAGCT[A/G]ACAGTCCAGGTGTCT | 51429 |
| rs112378365 | in-del | -/AG/GT/GTGTGT/GTGTGTGT | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157899892 | CACATGATTACCTAA[-/AG/GT/GTGTGT/GTGTGTGT]AGTGTGTGTGTGTGC | 51429 |
| rs112382880 | snp | C/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157882106 | TTTAAGGGGCTAATG[C/T]GGCTGGTAACTTTAT | 51429 |
| rs112386782 | snp | A/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157849640 | AGAAGTGAGTAGATT[A/G]TAGCAGTATTTAGAA | 51429 |
| rs112405189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157940717 | CCACTGCGCCCAGCT[C/T]AACTTGTTTTTCTAA | 51429 |
| rs112420750 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157944840 | TCAGAGCGTGGTAGC[C/T]GACTGTGAGGAAAAG | 51429 |
| rs112427878 | snp | A/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157935709 | TTAGAGTCCTCATCT[A/G]TTAGGCAAGATTTAT | 51429 |
| rs112428409 | snp | A/T | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157936405 | TCCCAGCTACTCGGG[A/T]GGCTGAGGTAGGAAG | 51429 |
| rs112465589 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157909316 | GTCTGTGATAGATTC[A/G]AAATTTTTAAAAACT | 51429 |
| rs112492116 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157765321 | GACTGTGGGGGCTTC[A/G]GGTGTTCATTTTGAA | 51429 |
| rs112533031 | in-del | -/CAGGCGGATCCC | 0.00279441 | 0.0372746 | intron-variant | SNX9 | GRCh38.p7 | 6:157756748 | CAGGCCCCCGAGACG[-/CAGGCGGATCCC]CAGGCGGATCCCCAG | 51429 |
| rs112533389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157819004 | TCCCGTTACTGTTTA[C/T]GGCTCTGTGTCTCCC | 51429 |
| rs112534033 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | SNX9 | GRCh38.p7 | 6:157913093 | GAGTTCATCGTATCC[C/G]AGGTCCAGACTGGCT | 51429 |
| rs112546322 | snp | C/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157820015 | AGAAGAAAATCTGAA[C/T]TTAGCATGGCCCAGG | 51429 |
| rs112548260 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | SNX9 | GRCh38.p7 | 6:157841962 | ACAGTGATCCTGGCC[A/C]GTTTTGTTTCCTCTA | 51429 |
| rs112568317 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | SNX9 | GRCh38.p7 | 6:157844547 | AGCCTCCAGCTACAT[A/G]ACTCCTAAATCATAA | 51429 |
| rs112594149 | in-del | -/TG | 0.0356815 | 0.128715 | intron-variant | SNX9 | GRCh38.p7 | 6:157907796 | CAGAGACTAACTCTT[-/TG]CTCTAAAAGTGCAGT | 51429 |
| rs112608761 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | SNX9 | GRCh38.p7 | 6:157942567 | GTGTAGACGCCTCCC[A/G]GCGGGAAGGGACCAC | 51429 |
| rs112640359 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SNX9 | GRCh38.p7 | 6:157835264 | GTGATCCACCTGCCT[C/T]GGCCCCTCAAAGTGC | 51429 |
| rs112673174 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SNX9 | GRCh38.p7 | 6:157765281 | TCCCACCACATTGCA[A/G]AGGTGCATGGAGGCA | 51429 |
| rs112682091 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | SNX9 | GRCh38.p7 | 6:157925438 | TTTGGCATTTACTGA[A/T]GTTGAACCCTCTCAT | 51429 |
| rs112683419 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157918935 | GTTATGAATCCAACA[A/G]TACATTGTGGTAATT | 51429 |
| rs112691994 | snp | A/C | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157865875 | GTGGGTGTTCAGTAA[A/C]TATTGTTAAATTAGT | 51429 |
| rs112704852 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157910855 | TAAAGGTTGTGTGCC[A/T]GGTGCAGTGGCATCC | 51429 |
| rs112705464 | snp | C/G | 0.0611083 | 0.163768 | intron-variant | SNX9 | GRCh38.p7 | 6:157851685 | CCCTCCACCTCCAGG[C/G]TTCAAGCGATTTTCC | 51429 |
| rs112712731 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157900176 | GACCTGTTAAAAGTT[C/G]CACATGTAAATAAGA | 51429 |
| rs112731661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157754913 | ATAGACAGAGCAGCC[C/T]CGAGGGCTGCTGGTT | 51429 |
| rs112735563 | in-del | -/T | 0.3752 | 0.216391 | intron-variant | SNX9 | GRCh38.p7 | 6:157878927 | CAGGCTGTCCTTTGG[-/T]GGGGGAAGGTACTAA | 51429 |
| rs112743752 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157761938 | GTGCTGAGAAAAGTT[C/T]GAGGGCATCAGAATG | 51429 |
| rs112746450 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157806554 | CATCTGTATCCTACC[A/G]TCTACCAAATAATCT | 51429 |
| rs112749962 | snp | A/C | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157941237 | AAGTTCCTTATTGTG[A/C]AGCTCCTTCCCCCCG | 51429 |
| rs112770747 | snp | C/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157918148 | TGATAGTGTTATTCA[C/G]GTTTCTATATCCTTG | 51429 |
| rs112773005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157906027 | TCTAGTGCACCCGAA[A/G]GACAGGACAAGGTTA | 51429 |
| rs112781647 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | SNX9 | GRCh38.p7 | 6:157916329 | GTGAGCCACCGTGCC[C/T]GGCCCTCTTTTCTTT | 51429 |
| rs112791659 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | SNX9 | GRCh38.p7 | 6:157798211 | GAAATTTTATACCCC[C/T]TGTGAGGGCGCAATG | 51429 |
| rs112800020 | snp | A/G/T | 0.0103295 | 0.0711199 | intron-variant | SNX9 | GRCh38.p7 | 6:157804576 | TGGAGTCTGAAAGTC[A/G/T]TCTGTTGGCAGAATT | 51429 |
| rs112812863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157850006 | AAGAAGAGTGTAGGA[C/T]CCTGGAAAACACAGA | 51429 |
| rs112834105 | in-del | -/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157815219 | AGGGCTGTCTGTGGG[-/T]TTTTTTTTTTTTAGA | 51429 |
| rs112834271 | in-del | -/CAGA | 0.5 | 0 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157944727 | GGAGTTGCCAAGAAG[-/CAGA]CAGTCTCCCAGTGTC | 51429 |
| rs112843756 | snp | C/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157757761 | ACTGGGAAGCTTGCA[C/G]CTGAACCAAGCTTTG | 51429 |
| rs112880879 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157935400 | CTCTAGGTCTAATAG[C/T]CAGTGTGAAGAGAAC | 51429 |
| rs112894974 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157781731 | AGAGAACTTCCCTTA[C/T]CACCGTCCCCCTTAT | 51429 |
| rs112915844 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157921468 | TGGTTTTTCAGTTAC[A/G]GTATGGTAACAGTCA | 51429 |
| rs112932453 | snp | C/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157909901 | TTCTCTTTCCCTTAT[C/T]TTGTAGAACACTAAT | 51429 |
| rs112948337 | in-del | -/T/TT/TTT | 0.259951 | 0.249802 | intron-variant | SNX9 | GRCh38.p7 | 6:157771703 | CTGGCTGGTAGGCAA[-/T/TT/TTT]TTTTTTTTTTTTTTA | 51429 |
| rs112948338 | in-del | -/CTCAGCCTCCCAA | 0.345925 | 0.230864 | intron-variant | SNX9 | GRCh38.p7 | 6:157913425 | AAGTGATCCTCCCAC[-/CTCAGCCTCCCAA]GTAGCTGGGATTATA | 51429 |
| rs112950811 | snp | G/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157867723 | CATTCGAGTCTGATT[G/T]TCCCATGTGGACTTA | 51429 |
| rs112991902 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | SNX9 | GRCh38.p7 | 6:157916330 | TGAGCCACCGTGCCC[A/G]GCCCTCTTTTCTTTT | 51429 |
| rs113026966 | in-del | -/TC | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157908178 | CTCAGCCGAAACAAA[-/TC]TCTCTTCCTTCAGCG | 51429 |
| rs113034872 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SNX9 | GRCh38.p7 | 6:157798489 | ACATTATTGGGATAA[C/T]TGGTGACATTTGAAC | 51429 |
| rs113035493 | in-del | -/C | 0.329317 | 0.237084 | intron-variant | SNX9 | GRCh38.p7 | 6:157919904 | TTGTTAAGTAACTTG[-/C]CCTAAGATTAAATCT | 51429 |
| rs113043603 | snp | A/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157777792 | GGGATTAGCTGTCAC[A/G]GCAGCCTCTGGAGTG | 51429 |
| rs113051296 | snp | G/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157874129 | GGACCTGTCTGCAGA[G/T]TGAGATCTAAGGCCG | 51429 |
| rs113073548 | in-del | -/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157796130 | TGGATTTAAGTGATC[-/T]TTTTTTTTTCTTAAT | 51429 |
| rs113079060 | snp | C/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157818511 | CAGTTTTAACCATCA[C/T]AGTTTGTAACTTGAG | 51429 |
| rs113086142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157923283 | AGAAACTATGATTCT[A/G]TGGTAAGTAGCAGCT | 51429 |
| rs113092501 | snp | C/T | 0.0108842 | 0.0729634 | intron-variant | SNX9 | GRCh38.p7 | 6:157936048 | CAGAACAGGTACTAA[C/T]ATAATCACACAATTC | 51429 |
| rs113101276 | in-del | -/TTAT | 0.00636936 | 0.0560724 | intron-variant | SNX9 | GRCh38.p7 | 6:157895466 | TCCGATCACATGGTA[-/TTAT]TTATAGTACCCAAAG | 51429 |
| rs113103839 | snp | A/T | 0.0581099 | 0.160244 | intron-variant | SNX9 | GRCh38.p7 | 6:157870638 | CACACATACCCACAC[A/T]CTCCTGCTCTCACAC | 51429 |
| rs113109776 | snp | C/G | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157762217 | ATCACCTGCCAACTG[C/G]CAGATCTGATTGTAG | 51429 |
| rs113115250 | snp | A/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157809635 | GCTTCTAAATAATAA[A/G]ACAAAAAACCTAATT | 51429 |
| rs113144980 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | SNX9 | GRCh38.p7 | 6:157794037 | TAGGCTAAGCTTTCT[C/T]GTGAAGAAGCTGATA | 51429 |
| rs113187865 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157861808 | AAGAGATGCACAAGA[A/G]TAACTAATAATAAAA | 51429 |
| rs113191470 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | SNX9 | GRCh38.p7 | 6:157851236 | GCACTCCAGCTTGGG[C/T]GACAGAGCAAGATGG | 51429 |
| rs113205294 | snp | C/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157828732 | CTTCCTCCTCAGCCC[C/T]GCAAAGTATTGGGAT | 51429 |
| rs113211618 | snp | A/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157870673 | GCAGCACTCACCTGT[A/G]CAAGCACATACACCC | 51429 |
| rs113213868 | snp | G/T | 0.0577344 | 0.159793 | intron-variant | SNX9 | GRCh38.p7 | 6:157858469 | TCACGTGATCCGCCT[G/T]TTTCGACTTCCCAAA | 51429 |
| rs113259572 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | SNX9 | GRCh38.p7 | 6:157913664 | GTGCTGCCCATCCCC[A/C]TGGTCCTAACCATGG | 51429 |
| rs113277153 | snp | A/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157844255 | GCAGTGCAGGAGACC[A/G]GAGTTTTATTATTAC | 51429 |
| rs113286806 | snp | A/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157833503 | ATGGTACTTAAGGAA[A/G]TTTTCTTCTTCCAGG | 51429 |
| rs113287764 | snp | A/G | 0.21725 | 0.247846 | intron-variant | SNX9 | GRCh38.p7 | 6:157835143 | TCAGCCTCCCAGGCA[A/G]CTGGGATTACAGATG | 51429 |
| rs113300455 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157900140 | CTTTCTGCTTCTATA[A/C]GTTTTTTAGATTTTT | 51429 |
| rs113306657 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157905988 | ATCTGATTACATTAG[A/G]TTTCATTTACCACAG | 51429 |
| rs113320890 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | SNX9 | GRCh38.p7 | 6:157870422 | CCTGCTCTCACACAC[A/G]CACACTCACATGCTG | 51429 |
| rs113342236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157769415 | CCAGCAGGAAGAGCA[C/T]GCTGGGGCGTGGGCA | 51429 |
| rs113387761 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157884253 | TATTTAAGGATATAA[C/T]ATTTTTCTCTACAGA | 51429 |
| rs113390383 | in-del | -/A | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157746359 | ACTTGTTTCCCCTTT[-/A]AAAAAAAAAAACATT | 51429 |
| rs113428013 | snp | A/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157934527 | TAAAATGGCATTTTA[A/T]ATGCCCCCAGGAGCG | 51429 |
| rs113428753 | snp | A/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157754590 | TGCGTCACACATTGT[A/G]TGAACTGAGCAACAT | 51429 |
| rs113428860 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SNX9 | GRCh38.p7 | 6:157942685 | AGACCAGTTAAAGAA[C/T]TGGAATTTGTGTCAT | 51429 |
| rs113443543 | in-del | -/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157810682 | ACCCTTGATGTTGGG[-/T]TTTTTTTTTTTCTGT | 51429 |
| rs113451866 | snp | G/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157802477 | AAGCACTCAGTAGAT[G/T]TCAGCTATTTCTGTT | 51429 |
| rs113467417 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant, downstream-variant-500B | SNX9, LOC105378078 | GRCh38.p7 | 6:157885055 | TTTAGGACTTTGAGC[G/T]ATCTGAGTAAGTAGA | 51429 |
| rs113468714 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888943 | TGAGGAGGAGTGTGG[G/T]ACCACGGAGAGAGGG | 51429 |
| rs113472268 | snp | A/C | 0.133777 | 0.221342 | intron-variant | SNX9 | GRCh38.p7 | 6:157840411 | TACAAAAAATACTTT[A/C]TTTCTTTCTTTTCTT | 51429 |
| rs113491032 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SNX9 | GRCh38.p7 | 6:157930561 | ATCACTCACATTACC[A/G]CCTGAGCTCCGCCTC | 51429 |
| rs113493789 | snp | A/G | 0.0225045 | 0.103662 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893940 | ATAGATCACTAAGAA[A/G]CAAGAGAGTCCAGCT | 51429 |
| rs113502303 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | SNX9 | GRCh38.p7 | 6:157841576 | GTGGGGTGTGGGGAT[C/T]GGGGCCAGTGAAGTA | 51429 |
| rs113509917 | snp | A/G | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157769611 | AGGAGCATCCCTCCC[A/G]AGGGCAGCGTGGGAG | 51429 |
| rs113518654 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157941845 | GGGAGACTAACTTAC[A/G]GGAGGAACTCACCTA | 51429 |
| rs113534487 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157750762 | CTACAACTCAACAGA[A/G]AAAAAAAAAACCCTA | 51429 |
| rs113546210 | in-del | -/C | 0.0123036 | 0.0774623 | intron-variant | SNX9 | GRCh38.p7 | 6:157874091 | CAGGAGAAAAGAATT[-/C]CCCCCCAGAGGATGT | 51429 |
| rs113553490 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157869086 | TGCATGCCAGTGTTT[C/T]TTACTGAATGTTTCC | 51429 |
| rs113575831 | snp | A/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157774242 | GAGGTGGAGGAGTGG[A/G]GGAGGTGGGGGAGTG | 51429 |
| rs113577565 | in-del | -/T | 0.0103295 | 0.0711199 | intron-variant | SNX9 | GRCh38.p7 | 6:157807637 | AGGTCAGGAATTGGA[-/T]TTTGCATTTAGGCCC | 51429 |
| rs113578966 | in-del | -/T | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157762711 | GGATGCAGTGGGGGT[-/T]GGGGGAAGTATTTTT | 51429 |
| rs113592257 | snp | C/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157811175 | AACAACTCACCTTCC[C/T]TGAAGTGAGTAAAGA | 51429 |
| rs113608889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157867060 | CTCAAGCAATCCTCC[C/T]GCCTCAGTTTTTTCA | 51429 |
| rs113626572 | in-del | -/TGTC | 0.271432 | 0.24908 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893520 | GACCAGCCACTAGGG[-/TGTC]TGTCCTACAACATTA | 51429 |
| rs113633287 | snp | A/G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157722582 | CATTTTTAGCAAAGC[A/G/T]CTTCTCTGTCTTTCC | 51429 |
| rs113636061 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | SNX9 | GRCh38.p7 | 6:157931897 | GGTGTCGCTAGAAGT[A/C]CTTTGTAAGCTAGAA | 51429 |
| rs113650054 | snp | A/C | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157791525 | TAAATAAATGAGAAT[A/C]ATGATTTTGCTTATG | 51429 |
| rs113651755 | snp | A/G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157774270 | GTGGAGGAGGTGGGG[A/G/T]AGTGGAGGAGGGATG | 51429 |
| rs113661786 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157787192 | CAACAATTTTTTTCC[-/T]GCCTTCAGATTCAAA | 51429 |
| rs113662169 | snp | A/G | 0.444444 | 0.157135 | intron-variant | SNX9 | GRCh38.p7 | 6:157740303 | GTCAGCCCAGGTCTT[A/G]CAGTAGAACAACTTG | 51429 |
| rs113695515 | snp | A/G | 0.5 | 0 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157901983 | AGAGTCAGCTGATGC[A/G]GGCGGCGCTCAGCGA | 51429 |
| rs113710023 | snp | G/T | 0.340485 | 0.23305 | intron-variant | SNX9 | GRCh38.p7 | 6:157938785 | AGGTGCTGGTGGAAG[G/T]TTTTTTTTCCCCAGC | 51429 |
| rs113720723 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157823827 | CGCTCTGTGGCGTCC[A/G]GCGTCCCCGCCGCCC | 51429 |
| rs113730476 | in-del | -/TTACAAGGGTCA | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157901019 | CTGTTTATAGGCTCT[-/TTACAAGGGTCA]CTTTCCATTCCCAGA | 51429 |
| rs113732924 | snp | A/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157766934 | TTTTGAAAATTAGAA[A/T]TATATATAGGTAAAT | 51429 |
| rs113741186 | snp | C/T | 0.00121241 | 0.0245913 | intron-variant | SNX9 | GRCh38.p7 | 6:157921681 | GACATTGTGTTAATA[C/T]GGCATCAGAGAATAT | 51429 |
| rs113758802 | snp | A/G | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157794820 | ATTAGTATTTAGCTT[A/G]TATTTATATTGTCTT | 51429 |
| rs113764356 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157778987 | ACGTGGTGAAGGCTT[A/C]CCTGTCACAATCCCT | 51429 |
| rs113780044 | in-del | -/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157760033 | CACCACACTGGCTAA[-/T]TTTTTTTTATCTTTT | 51429 |
| rs113787024 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SNX9 | GRCh38.p7 | 6:157878813 | CAAAAATACTTCTGA[C/T]TTATGACGGATACAG | 51429 |
| rs113819203 | snp | C/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157731008 | TATTATTATTATTAT[C/T]TCTGAGAAAGAGTCT | 51429 |
| rs113821944 | snp | A/C | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157936981 | CTGATACTTCTAAAA[A/C]AGCATTCATTTTAAT | 51429 |
| rs113823340 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157936170 | TTCTGTGTATCTTTT[A/T]TAATTGTGTTTAATC | 51429 |
| rs113833439 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SNX9 | GRCh38.p7 | 6:157802876 | GAACTTGCAACACCC[C/T]TGGACATTAGAGAGG | 51429 |
| rs113839599 | snp | A/G | 0.245061 | 0.249951 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157891249 | GGCTAGGCTGGTCTC[A/G]AACTCCTGACCTCAA | 51429 |
| rs113849691 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SNX9 | GRCh38.p7 | 6:157930282 | GGAATAACAGTTGTT[C/T]CTTTCCCATGGCAAA | 51429 |
| rs113873630 | snp | A/C | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157787443 | CTCTCTCTCCCCCCC[A/C]CCCCTCTCTCTGTGT | 51429 |
| rs113894065 | snp | A/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157835594 | TCTCATCTTGAATTG[A/T]AATCGCTGTAATCTC | 51429 |
| rs113915838 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157905463 | CTCTAATTTCAGAAA[A/T]GTCCTTTGGATATAG | 51429 |
| rs113922092 | snp | C/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157891278 | AAGTGATCCTCCTGC[C/G]TCAGCCTCCCAAAAT | 51429 |
| rs113933265 | snp | C/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157849347 | ATAAGCCATGCTTAT[C/T]AACATTGGGGTTTAT | 51429 |
| rs113975348 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | SNX9 | GRCh38.p7 | 6:157840077 | GTGTCTTTGGATCTC[A/G]GGAAAGAGCAGACCC | 51429 |
| rs113979519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157837145 | AGAAAATCACAGATC[C/T]GTAAAATATTCTCAG | 51429 |
| rs114004794 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | SNX9 | GRCh38.p7 | 6:157826560 | TTAAGGGGATTATCT[A/G]TTTTCTATTTCTACT | 51429 |
| rs114008739 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SNX9 | GRCh38.p7 | 6:157912154 | GTTTTCTCTTAAAAA[A/G]TACAGATTTCTTTCC | 51429 |
| rs114022568 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SNX9 | GRCh38.p7 | 6:157811959 | TTGAGAATTTATATG[C/T]AAGCTCAGTCATGTG | 51429 |
| rs114025140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888750 | AAGTGATTATGTCAG[A/G]TAAAGTATCTTACAG | 51429 |
| rs114040204 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | SNX9 | GRCh38.p7 | 6:157748983 | TCAGAGACATTATCT[C/T]AATTACCTTCTTACA | 51429 |
| rs114064314 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | SNX9 | GRCh38.p7 | 6:157836119 | AATTTTTTGTTTGTT[G/T]GTTTGTTTGTTTGTA | 51429 |
| rs114091454 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157807368 | TCTCTGTCACTTAAA[A/T]TATTCAATTGTAAAT | 51429 |
| rs114092837 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157773961 | GATATTCCTGGACAC[A/C]CTCTCTGGAGTTTGG | 51429 |
| rs114119020 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SNX9 | GRCh38.p7 | 6:157883300 | TACACTGGGGGACCA[A/G]AAAAGTCCACATGAC | 51429 |
| rs114124491 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SNX9 | GRCh38.p7 | 6:157939967 | GAGTTGGGGGCAGGG[A/G]CAGGGGGGACAGAGA | 51429 |
| rs114165937 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SNX9 | GRCh38.p7 | 6:157778355 | TCTGCAAATACCTTA[C/T]TTCCAAGTATCTTTT | 51429 |
| rs114166063 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | SNX9 | GRCh38.p7 | 6:157759882 | TTGTTTTTTGTTTTC[C/T]TTTTTAGATGGAGTC | 51429 |
| rs114193625 | snp | A/C/G | 0.0146672 | 0.084371 | intron-variant | SNX9 | GRCh38.p7 | 6:157731943 | CTGCTGGGAATGCCA[A/C/G]TCAGGGAAGCAGGAG | 51429 |
| rs114213098 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | SNX9 | GRCh38.p7 | 6:157915053 | TTTGGAAAGACAGAT[A/C]TGTTTTCCATTTATT | 51429 |
| rs114246504 | snp | A/C/G | 0.00953873 | 0.0683987 | intron-variant | SNX9 | GRCh38.p7 | 6:157825430 | TGAAATTTTTATTTC[A/C/G]TAGTTAATCCTGAAC | 51429 |
| rs114249926 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SNX9 | GRCh38.p7 | 6:157847381 | ATGCTAGAATCACAG[C/T]TGTGAGCCACTGCGC | 51429 |
| rs114261460 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157870269 | TCTCTCACATCCCCA[C/T]GCTCATGCTCTCACA | 51429 |
| rs114279454 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157765015 | GTGCAAAAGTAACTG[C/T]GGTTTTTACCATTAC | 51429 |
| rs114281053 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157716320 | AAAAAACCATCATGC[C/T]GGCCATCACGTTTTA | 51429 |
| rs114324976 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SNX9 | GRCh38.p7 | 6:157824391 | ACTGATCTGTGATAC[A/G]CTGTGAGGAGTGGGT | 51429 |
| rs114325252 | snp | A/C | 0.0603597 | 0.1629 | intron-variant | SNX9 | GRCh38.p7 | 6:157844001 | TGCCTTAGCCTCCTG[A/C]ATAGCTGGGATTACA | 51429 |
| rs114338621 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | SNX9 | GRCh38.p7 | 6:157786112 | CGGTGGCACAATCAT[A/T]GCTCACTGTAGCCTT | 51429 |
| rs114352126 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | SNX9 | GRCh38.p7 | 6:157819570 | CATCACACATTTTCA[A/C]TCCGTTCCACATTAG | 51429 |
| rs114363482 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157804568 | GATGTTGTTGGAGTC[A/T]GAAAGTCGTCTGTTG | 51429 |
| rs114380008 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SNX9 | GRCh38.p7 | 6:157812429 | TAAGATCAATTTAGT[C/T]ACATGTTTAATTTTT | 51429 |
| rs114387445 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SNX9 | GRCh38.p7 | 6:157851739 | GGATTACAGGCGTTC[A/G]CTACCACACCCAGCT | 51429 |
| rs114392289 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SNX9 | GRCh38.p7 | 6:157884133 | ATTCTCCCATCTGAC[A/G]GGCTACCCAATCAAA | 51429 |
| rs114403648 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | SNX9 | GRCh38.p7 | 6:157806587 | AAATCAAGTAAAAAA[A/T]GGCAGCTGGTAGCAT | 51429 |
| rs114439756 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | SNX9 | GRCh38.p7 | 6:157741772 | CCTCACGGCGGGAAG[G/T]CTTCCCCCAAGGAAG | 51429 |
| rs114448058 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SNX9 | GRCh38.p7 | 6:157859646 | CCCCAAATTGTGGCC[A/G]TGGGGATCTGGCAAT | 51429 |
| rs114519002 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157742565 | TGTTGTCAGAATCAC[C/T]TGGAGTGCTGATTAA | 51429 |
| rs114528939 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SNX9 | GRCh38.p7 | 6:157866818 | CTTAGATGTGTGTGC[A/G]TGTGTGTATGTCTCT | 51429 |
| rs114544258 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157785510 | TGTAACCAACTATAT[A/T]AACAGAATAAAGGAT | 51429 |
| rs114548261 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157833076 | GGACAGTTGACATTC[A/G]GATATTAATGAATTG | 51429 |
| rs114578490 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SNX9 | GRCh38.p7 | 6:157766608 | AGATTCCTAACTACT[A/G]TCTTGGAATCCCATC | 51429 |
| rs114584978 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | SNX9 | GRCh38.p7 | 6:157743085 | AAAGTGGAAAAAAAT[A/T]TAATCCACAGATAAC | 51429 |
| rs114589072 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SNX9 | GRCh38.p7 | 6:157909449 | GGGCTGAGCTACTCA[C/T]GTGGGAGCAGAAGGG | 51429 |
| rs114604247 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | SNX9 | GRCh38.p7 | 6:157741116 | CTTTGGGAGGCTGAG[A/G]CAGGGGGATTGCTTG | 51429 |
| rs114663941 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | SNX9 | GRCh38.p7 | 6:157797390 | ACACAATAGTAATAA[C/T]ATAAAGCATATGCTT | 51429 |
| rs114670376 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | SNX9 | GRCh38.p7 | 6:157883587 | GTTCTATTTCTGTGA[C/T]GCCTCAGTGTGGCTA | 51429 |
| rs114720747 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | SNX9 | GRCh38.p7 | 6:157760209 | TGTCTGAGTGGAGGA[A/C]GCATTATATAACCCT | 51429 |
| rs114729639 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | SNX9 | GRCh38.p7 | 6:157778756 | AGAATTTTTACCCAG[A/G]TCCAACTGATGCAAA | 51429 |
| rs114775300 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | SNX9 | GRCh38.p7 | 6:157745337 | TTAGTGGCAGTGATC[A/G]TCATCGTAATAGCCA | 51429 |
| rs114817088 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | SNX9 | GRCh38.p7 | 6:157931777 | CAGCATTTATTAGCC[A/G]TGTGACCTTGGGCAA | 51429 |
| rs114822894 | snp | A/T | 0.0475351 | 0.146656 | intron-variant | SNX9 | GRCh38.p7 | 6:157926388 | TATCTTAATATTTTT[A/T]AAAAAATAGCTCATA | 51429 |
| rs114828795 | snp | A/C | 0.146314 | 0.227484 | intron-variant | SNX9 | GRCh38.p7 | 6:157865060 | CAAAAACTACCGCAG[A/C]CAGGCATGGTGGCTC | 51429 |
| rs114839514 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893261 | AGTCCATCCCGAAGC[C/T]GAATGTCACCTTGTA | 51429 |
| rs114841635 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | SNX9 | GRCh38.p7 | 6:157829643 | TTCTCTACATTTACA[A/G]TTAGTATTATTTTCT | 51429 |
| rs114857086 | snp | G/T | 0.0558544 | 0.157504 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157895122 | AACATCCATCCTTGT[G/T]GACTTTGAGGTGAGA | 51429 |
| rs114898869 | snp | C/T | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894106 | TTTCGCTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 51429 |
| rs114923103 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SNX9 | GRCh38.p7 | 6:157824721 | ACCTGTTGCTGCTGT[C/T]ACTGAAATAATTACC | 51429 |
| rs114943185 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | SNX9 | GRCh38.p7 | 6:157767029 | TTCAACTGTTACTAG[C/T]GCTGCTTCTCCTCCT | 51429 |
| rs114944540 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | SNX9 | GRCh38.p7 | 6:157812442 | GTTACATGTTTAATT[G/T]TTTGTCCTTGTGTGA | 51429 |
| rs114973555 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | SNX9 | GRCh38.p7 | 6:157730119 | GATAAATGCATAACT[C/G]TGTTAATACACTAAA | 51429 |
| rs115026368 | snp | C/T | 0.00755907 | 0.0610114 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821997 | AAGGATTAAATGAGA[C/T]GGGGATGTGGAAGCC | 51429 |
| rs115046486 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SNX9 | GRCh38.p7 | 6:157908631 | CCAGGTTCCTCTGCA[A/G]CTGCCCCCATGGCCT | 51429 |
| rs115049231 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889822 | TTTACTCAAAGAAAT[A/G]CTAGTCTTTATTCTT | 51429 |
| rs115049588 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | SNX9 | GRCh38.p7 | 6:157927497 | TGTGATGAAACCAAG[C/G]GGCATGGAGCCACCT | 51429 |
| rs115084502 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157929315 | TGGCCCAGGATAGAA[A/G]AATAGTCCCGTATCC | 51429 |
| rs115105000 | snp | C/G | 0.0391387 | 0.134304 | intron-variant | SNX9 | GRCh38.p7 | 6:157803969 | GGTTCAAGCCATTCT[C/G]CTGCCTCAGCTACTC | 51429 |
| rs115115129 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SNX9 | GRCh38.p7 | 6:157835893 | AACAGACTAATACAG[C/T]CTGGGACCACAGGCA | 51429 |
| rs115130094 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157744648 | AAGGCTTGCGACAGC[C/T]CCCCCAGCACTTCAG | 51429 |
| rs115148241 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | SNX9 | GRCh38.p7 | 6:157764606 | TTGTCATATGGAACC[C/T]TCCTACACAGTCTGT | 51429 |
| rs115161824 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | SNX9 | GRCh38.p7 | 6:157769116 | ACACAAGCAGTGGAC[A/G]CTTTGGTGAGCAGTA | 51429 |
| rs115162125 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SNX9 | GRCh38.p7 | 6:157717155 | TAGCTCACTGAAGCC[A/G]CAAACTCCTGGCTCA | 51429 |
| rs115168501 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | SNX9 | GRCh38.p7 | 6:157806994 | CCCCAGTCCTTTAAT[A/G]AGCTACCTGCATTCC | 51429 |
| rs115199332 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SNX9 | GRCh38.p7 | 6:157773371 | CGAGGTGCAGAGGTC[A/G]CATGTCCAGAGGCAC | 51429 |
| rs115227114 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | SNX9 | GRCh38.p7 | 6:157757375 | GGGGCCTTATCCACG[A/G]CACTCTGTTACCGGG | 51429 |
| rs115237694 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | SNX9 | GRCh38.p7 | 6:157826574 | TATTTTCTATTTCTA[A/C]TCCTTACTCAGTAGA | 51429 |
| rs115249165 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SNX9 | GRCh38.p7 | 6:157908382 | TTCATTCTCTTCTTG[A/G]ATTATAACTCAATTA | 51429 |
| rs115299892 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | SNX9 | GRCh38.p7 | 6:157751038 | AATGGTGCAGCCACT[A/G]TGGAACATGGTATGG | 51429 |
| rs115356228 | snp | A/G | 0.00716266 | 0.059414 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157943445 | TAGTGCCATCGTGGT[A/G]TGTGGCAGGTGGGCC | 51429 |
| rs115378133 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157935367 | AACTGAACTGGTGGT[A/G]TGTGACTCTGATCAG | 51429 |
| rs115389437 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | SNX9 | GRCh38.p7 | 6:157829406 | ATTTGTTGAGGCTAA[A/C]TTTATTCCCAGCATA | 51429 |
| rs115391264 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | SNX9 | GRCh38.p7 | 6:157852980 | TTCTTTCAGAAAAAT[G/T]AAATGGTGAGTTTTT | 51429 |
| rs115414607 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | SNX9 | GRCh38.p7 | 6:157754988 | TGAATCTCATGTCTC[C/T]CCTTTTTAGACCATG | 51429 |
| rs115426227 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | SNX9 | GRCh38.p7 | 6:157901795 | CCATCAAAAAAAAAT[C/T]GATTTGCCCAGTAGG | 51429 |
| rs115448252 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | SNX9 | GRCh38.p7 | 6:157845233 | CCTGCCTCAGCTTTC[C/T]GAATAGCTGGGCTTA | 51429 |
| rs115461971 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | SNX9 | GRCh38.p7 | 6:157729563 | TAGAATATAAAAAAG[A/T]TAGAATTTCTGACAG | 51429 |
| rs115475375 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | SNX9 | GRCh38.p7 | 6:157925292 | AATACACATTAAAAC[C/T]ACAATAAGATGCCAC | 51429 |
| rs115499112 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | SNX9 | GRCh38.p7 | 6:157740513 | TGAAGCACACAGCAC[C/T]CCAATGCAGAGGGGG | 51429 |
| rs115527594 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157775592 | CCCCAGCAGTTACCT[C/T]CATTTTTCCCCCAAT | 51429 |
| rs115590812 | snp | A/G | 0.0437281 | 0.141251 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157895108 | AGGTAAACATATGTA[A/G]CATCCATCCTTGTTG | 51429 |
| rs115655934 | snp | A/G | 0.00463696 | 0.0479268 | intron-variant | SNX9 | GRCh38.p7 | 6:157936057 | TACTAACATAATCAC[A/G]CAATTCCAATTAAGA | 51429 |
| rs115662700 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | SNX9 | GRCh38.p7 | 6:157799328 | TGTGTGTGTGGAGAG[A/G]TATGTGTACATGCAC | 51429 |
| rs115673192 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | SNX9 | GRCh38.p7 | 6:157825622 | GGCTGCCTAATCACT[A/G]TTCCACATGGTGCTC | 51429 |
| rs115688270 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SNX9 | GRCh38.p7 | 6:157867195 | TGGCCTCAAGCAATC[C/T]TCCTGCTATTTAGTC | 51429 |
| rs115799391 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157763410 | GCGGGGAAGTACCTG[C/T]TCCCTCTTCTAACAA | 51429 |
| rs115802835 | snp | A/G | 0.039522 | 0.134904 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822475 | AGATGGAAAATTTTA[A/G]AGACCTCGTTTCCAC | 51429 |
| rs115805678 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157780383 | GGGGTGACTCTTGGC[A/G]TGGCCTGTGATTTGG | 51429 |
| rs115819596 | snp | G/T | 0.145642 | 0.227177 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822856 | AAAGCGCCGAGCCAC[G/T]GCGTGCGGCGCCGGC | 51429 |
| rs115828561 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | SNX9 | GRCh38.p7 | 6:157828969 | ACTTTTGTATCTTCA[A/T]TGACAAGTTTAAAAG | 51429 |
| rs115833502 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | SNX9 | GRCh38.p7 | 6:157728024 | TGGCCTCAAGTTGTC[C/G]GTAAAATTCAGCTAT | 51429 |
| rs115861898 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157764628 | ACAGTCTGTTTTTCC[C/T]CTGGAGCTGACGATG | 51429 |
| rs115863060 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SNX9 | GRCh38.p7 | 6:157750445 | CATGCAAATTGTATC[C/T]TTATCTTACACCATA | 51429 |
| rs115883302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157857428 | TGCTCGGAATTCCCA[A/G]TCTGGGCACTAGATA | 51429 |
| rs115930842 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | SNX9 | GRCh38.p7 | 6:157722620 | AAGGATAGGCAGGAG[G/T]CGGATGAATCGGAGC | 51429 |
| rs115936059 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890982 | AGACACTGTTATTTT[A/G]AGGGTACTCATAGTG | 51429 |
| rs115950955 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | SNX9 | GRCh38.p7 | 6:157882831 | AGATGGAATCTATTC[A/G]TGGTGAGGATGCTAT | 51429 |
| rs115954868 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | SNX9 | GRCh38.p7 | 6:157915922 | AGTTATGTATTGCAT[A/G]TAGAGATCGCTTGAT | 51429 |
| rs116006642 | snp | A/G | 0.039522 | 0.134904 | intron-variant | SNX9 | GRCh38.p7 | 6:157817878 | AGACTCTGACTCTAA[A/G]TAAATAAATAAATAA | 51429 |
| rs116014752 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157919524 | TTTATTTCAATTACT[A/C]TACTTTCAACTCCAG | 51429 |
| rs116022207 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SNX9 | GRCh38.p7 | 6:157833083 | TGACATTCAGATATT[A/G]ATGAATTGGTGTATT | 51429 |
| rs116026228 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | SNX9 | GRCh38.p7 | 6:157770907 | AAATTATTGTTGTAA[A/G]GGTTTAAAAGACAAT | 51429 |
| rs116056926 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | SNX9 | GRCh38.p7 | 6:157782073 | CACCAAGATGGGTCC[A/G]CATGTAGACCTTACT | 51429 |
| rs116059630 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | SNX9 | GRCh38.p7 | 6:157742361 | CTCTGTGTTCTGAAC[A/G]CCACTGGGCTTCTCC | 51429 |
| rs116064813 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157776164 | TTTTGAATAATAGAC[A/G]CCAACCCATACTAGT | 51429 |
| rs116065165 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | SNX9 | GRCh38.p7 | 6:157758384 | TTGGGAGAATATTAT[A/T]CAGGGAAATGGCAAT | 51429 |
| rs116135044 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | SNX9 | GRCh38.p7 | 6:157740720 | AGCTCACAACTGCCA[C/T]TGGTTTCCCACAGTT | 51429 |
| rs116208589 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | SNX9 | GRCh38.p7 | 6:157767634 | TTATTTGGGTTTTTT[A/G]GGAACTGAAATTTGC | 51429 |
| rs116212253 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | SNX9 | GRCh38.p7 | 6:157837826 | GTGAAGCCGTCGTTG[A/G]CATTTAAACAAGGTG | 51429 |
| rs116213735 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SNX9 | GRCh38.p7 | 6:157830526 | GTGTGGATTTTAGTT[A/G]CACAGCTTGGGTTTC | 51429 |
| rs116214724 | snp | A/C | 0.0279526 | 0.114869 | intron-variant | SNX9 | GRCh38.p7 | 6:157916417 | TCCATGGGCCTTCTA[A/C]TTCTGTTTCTGCCTT | 51429 |
| rs116216650 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | SNX9 | GRCh38.p7 | 6:157883745 | ACTCCTTCCATCTTT[C/G]AGAAGCCCATCTCTT | 51429 |
| rs116225630 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | SNX9 | GRCh38.p7 | 6:157828983 | AATGACAAGTTTAAA[A/G]GAGCAAAAATATATT | 51429 |
| rs116227198 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157873955 | CGGTCCCTCCAAACC[A/G]AGCGAAGGTTCTTGG | 51429 |
| rs116248979 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157754714 | ACCTGTGCAGCTATC[A/G]CAACCTCAAAGCATC | 51429 |
| rs116285134 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886009 | AACCTAGCCCTCCTT[C/T]GAGGCCTGATGTAGT | 51429 |
| rs116317333 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | SNX9 | GRCh38.p7 | 6:157825319 | GATCTGTCTAGTGGT[G/T]GTCAGTGTGTTTTTA | 51429 |
| rs116366847 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157790111 | CACTCCCACGCCCTT[G/T]CCGCTTATTTACCAT | 51429 |
| rs116395741 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157772619 | GTTTTGGACTTCCAG[A/C]CTTCAGAACTGGGGG | 51429 |
| rs116405786 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | SNX9 | GRCh38.p7 | 6:157769892 | GAAGAAGGAGAGCAC[C/T]AGGGGTCTGAAAGCA | 51429 |
| rs116432244 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | SNX9 | GRCh38.p7 | 6:157872852 | CAAGATGAGGGTCAT[C/G]TAATCATCAGCTGTT | 51429 |
| rs116436601 | snp | A/G | 0.0111196 | 0.0737302 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157944740 | AGCAGACAGTCTCCC[A/G]GTGTCTGACTCTCGG | 51429 |
| rs116440941 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | SNX9 | GRCh38.p7 | 6:157898658 | AATGGGAAATAATTT[A/G]GGAATTAAGGGTATT | 51429 |
| rs116525104 | snp | A/G/T | 0.0168055 | 0.0901129 | intron-variant | SNX9 | GRCh38.p7 | 6:157879499 | AATCAAACTCTCTTC[A/G/T]TTTTCTTATTCAAAT | 51429 |
| rs116527604 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | SNX9 | GRCh38.p7 | 6:157915885 | ATTGTAAATGGTACT[A/G]TTTTTTAAATTTCCA | 51429 |
| rs116548081 | snp | C/T | 0.0158469 | 0.0875917 | upstream-variant-2KB, downstream-variant-500B | SNX9, LOC107986663 | GRCh38.p7 | 6:157715144 | CTGAAAGAATTGCGG[C/T]CGTGAATAAACATTT | 51429 |
| rs116596007 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SNX9 | GRCh38.p7 | 6:157920475 | TCCACCCTAGTGGTA[C/T]CACCATGTCGAACAC | 51429 |
| rs116606235 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157787738 | TTTGTATAAATATTT[A/G]AATTCAAAAATAAAG | 51429 |
| rs116616143 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | SNX9 | GRCh38.p7 | 6:157882679 | GAAGGAAGTAACTGC[A/G]GATGTGGTAGAAATA | 51429 |
| rs116638454 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | SNX9 | GRCh38.p7 | 6:157716970 | AGCAATCCCATGCCC[A/G]TCTGTCATCTCCGCA | 51429 |
| rs116673763 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157862633 | AAGAATGGGGCCTTA[A/G]CTTTTGCATTCTAAC | 51429 |
| rs116675752 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | SNX9 | GRCh38.p7 | 6:157786097 | AGCCAGGCTGGAGTG[C/T]GGTGGCACAATCATA | 51429 |
| rs116676092 | snp | A/C | 0.0225045 | 0.103662 | intron-variant | SNX9 | GRCh38.p7 | 6:157750635 | ACTAGAAAGCTTCTG[A/C]ACAGCAAAGGAAATA | 51429 |
| rs116687070 | snp | A/C | 0.0379877 | 0.132479 | intron-variant | SNX9 | GRCh38.p7 | 6:157809045 | CAAATAAATCTCTAT[A/C]AACCAAAGAAATTGA | 51429 |
| rs116705376 | snp | G/T | 0.021333 | 0.101051 | intron-variant | SNX9 | GRCh38.p7 | 6:157770842 | TTATTTGGCTAAGAA[G/T]TTCATAGGATGCCTG | 51429 |
| rs116710800 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | SNX9 | GRCh38.p7 | 6:157727427 | TCTAAGTCTGATCAA[C/G]CTGTGAGGGCCCCAG | 51429 |
| rs116712906 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | SNX9 | GRCh38.p7 | 6:157801802 | TGTGTCTGATGAGAA[C/T]GCGTGCTCTGACAGA | 51429 |
| rs116718065 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | SNX9 | GRCh38.p7 | 6:157831637 | GTGGAGTCTCCCAGC[A/G]GGAAATCCTGCCTCA | 51429 |
| rs116718197 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | SNX9 | GRCh38.p7 | 6:157741491 | TTTAACAATGGCCCC[C/T]AGGTGATTCTGATGT | 51429 |
| rs116770044 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | SNX9 | GRCh38.p7 | 6:157792535 | GTGGCTAAATGAAAC[C/T]AACATGTGCACTACT | 51429 |
| rs116774572 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | SNX9 | GRCh38.p7 | 6:157812480 | GCAGACAGTGTATTT[A/G]CCAAACCCATTTCCT | 51429 |
| rs116807695 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SNX9 | GRCh38.p7 | 6:157931443 | CTTTTGAAAGGCAAA[C/T]AGATGCTCCATTTAA | 51429 |
| rs116854762 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890082 | AAGTTCTTAACCACT[A/G]TCCCCATGTGGTATA | 51429 |
| rs116896274 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157754607 | GAACTGAGCAACATG[C/T]ATGTTGTGAGCGTGG | 51429 |
| rs116897236 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SNX9 | GRCh38.p7 | 6:157941651 | AGCTCCCCTCTGGCC[A/G]TGGGATCTAAGCCAT | 51429 |
| rs116923654 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | SNX9 | GRCh38.p7 | 6:157774537 | CCTGCGGTCATCGAC[C/T]CACGTGTCTGCCTTA | 51429 |
| rs116950209 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, downstream-variant-500B | SNX9, LOC105378078 | GRCh38.p7 | 6:157884892 | CTTAAAACTGCAGTG[A/G]TGAAGGACCAGCCAG | 51429 |
| rs116967026 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | SNX9 | GRCh38.p7 | 6:157858605 | AGGATTTACTGTGGC[C/T]ATTGTTACAATCTAC | 51429 |
| rs116973102 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SNX9 | GRCh38.p7 | 6:157849528 | AAGATGAATTGGAGC[A/G]AGGCGCAGCAGGTGT | 51429 |
| rs117018570 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157760543 | GGGTGACAGCCAAGC[A/G]TTTAGACAAGGACAG | 51429 |
| rs117036589 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | SNX9 | GRCh38.p7 | 6:157771785 | GCTCACTGCAAACTC[C/T]GCCTCCCAGGCTCAA | 51429 |
| rs117038393 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157733012 | TATTTTATTTGGCCT[A/G]ACACCCTCTAGGTTC | 51429 |
| rs117046724 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890444 | TTTGCATTATGAGGA[A/G]AGGATAGCTTTTAAA | 51429 |
| rs117101496 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SNX9 | GRCh38.p7 | 6:157843050 | AAAGGTTACAAGCAA[A/G]ATAGAGTTGGTTAGG | 51429 |
| rs117156768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157765809 | GCTGTAATATTTATT[C/T]ACAGGGGAGCTTTGG | 51429 |
| rs117173190 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | SNX9 | GRCh38.p7 | 6:157832945 | CCATAGTACAGCTCC[A/G]CAGTCTGCAAGTCCA | 51429 |
| rs117195949 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157772496 | GTGGGGTGATGCATC[C/T]GCAGGCTAAGGACCA | 51429 |
| rs117201021 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157809939 | CCTCTTATCATATGA[C/T]CACTCAATTTCATTT | 51429 |
| rs117242059 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | SNX9 | GRCh38.p7 | 6:157865744 | GCTTTTTTTTCTTAG[G/T]CTGTTATCACTAAAT | 51429 |
| rs117269092 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157841679 | CATGTTGAGGAACTG[G/T]GAGGAGGTGTAGAAC | 51429 |
| rs117314600 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157880993 | TTATAGTTATCTCAT[A/G]TACCACTGCTTCTAA | 51429 |
| rs117332983 | snp | A/C | 0.0494327 | 0.149241 | intron-variant | SNX9 | GRCh38.p7 | 6:157784180 | AGAAATGTCAGAATT[A/C]AATGAAATAGAAAAT | 51429 |
| rs117402198 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | SNX9 | GRCh38.p7 | 6:157859673 | CAATGTCTGCCAGAT[G/T]AATTTGTCTCTCTTA | 51429 |
| rs117413572 | snp | C/T | 0.147991 | 0.228242 | intron-variant | SNX9 | GRCh38.p7 | 6:157844038 | TACCTCCTCACCTGC[C/T]TAATTTTTGTATTTT | 51429 |
| rs117445094 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | SNX9 | GRCh38.p7 | 6:157733395 | TGAGGCAGGAGAAGG[G/T]CATGAATCCGAGGGG | 51429 |
| rs117454311 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SNX9 | GRCh38.p7 | 6:157769190 | TCCAAGGATGCTCCT[C/T]GGGCCTCCCATGCAG | 51429 |
| rs117472144 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | SNX9 | GRCh38.p7 | 6:157902238 | AAGGATTTTTGATTT[A/G]CAAGGTTAATAAGTG | 51429 |
| rs117476763 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SNX9 | GRCh38.p7 | 6:157869078 | GAGAGGTCTGCATGC[C/T]AGTGTTTCTTACTGA | 51429 |
| rs117509283 | snp | A/G | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157891792 | CTTTGCTAAATTGAG[A/G]AAGATGAGGTGTGCA | 51429 |
| rs117510189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157841292 | GTGTGTTTTAATTTA[A/G]GGTCTTCAAGATGAA | 51429 |
| rs117510260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893871 | AATAAACAGCTAAGA[A/G]ATGTTATGCTAAAGT | 51429 |
| rs117518010 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157892040 | TAATTACCCATGATG[A/G]ACAGTTAAGAGCTTT | 51429 |
| rs117527378 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | SNX9 | GRCh38.p7 | 6:157717809 | TTTAGTTTTATTAAA[G/T]GTTTTATTTTTATGG | 51429 |
| rs117540692 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SNX9 | GRCh38.p7 | 6:157751702 | AATAAGCCAGACACA[A/G]AAAGACAAATGCTGC | 51429 |
| rs117545476 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SNX9 | GRCh38.p7 | 6:157799098 | CAAGGCAGCAGGAGG[A/G]AGGGTGTGCAAGAAC | 51429 |
| rs117547970 | snp | A/G | 0.0693013 | 0.172766 | intron-variant | SNX9 | GRCh38.p7 | 6:157772243 | GGGGTGAAGGAGGCA[A/G]TGGGACTCCCAGCAG | 51429 |
| rs117556550 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157795058 | ACTAGAAACTGAACA[A/G]TCATATGCAGTATGT | 51429 |
| rs117578520 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157804137 | GTGCTCATATTACAG[A/G]CGTGATCCACCACGC | 51429 |
| rs117675311 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890588 | GTGATTACATAGATT[G/T]AAGCGTGTCCCAGAG | 51429 |
| rs117691654 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SNX9 | GRCh38.p7 | 6:157875237 | ACAGAGCGTATTTGT[A/G]AAGGCTTGTGATGCA | 51429 |
| rs117692239 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | SNX9 | GRCh38.p7 | 6:157942032 | AATTTTGATAGTGTT[C/G]ATTTATTGATTTTCA | 51429 |
| rs117719757 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | SNX9 | GRCh38.p7 | 6:157912902 | CTAATTATTTGCAAC[G/T]TGGTCTGAAAATTCT | 51429 |
| rs117721194 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | SNX9 | GRCh38.p7 | 6:157923983 | GTGGCGGATCACTTG[A/C]GGTCAAGAGTTCGAG | 51429 |
| rs117731909 | snp | A/G | 0.128288 | 0.218372 | intron-variant | SNX9 | GRCh38.p7 | 6:157900501 | AATAGACACACACAA[A/G]ATAGCGAAAGCTGGG | 51429 |
| rs117734348 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888009 | TACCTCTTCTCACAA[A/G]ATGCTGTATTGTAGG | 51429 |
| rs117734550 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157788941 | GCCAATTGTAAAGAA[G/T]AAACAAAATAATTAT | 51429 |
| rs117737003 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SNX9 | GRCh38.p7 | 6:157816682 | ACTCTGTAGTCATTG[A/G]AAAACAGCATCTTGG | 51429 |
| rs117743436 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | SNX9 | GRCh38.p7 | 6:157903372 | CTTCAGTGATTAAAT[G/T]AGTTCTCTTTTGACT | 51429 |
| rs117753825 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SNX9 | GRCh38.p7 | 6:157876919 | CCAAGTGTTGCCTAG[A/G]AGCAAAGCCAAGCCA | 51429 |
| rs117812058 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SNX9 | GRCh38.p7 | 6:157830840 | TGGAACTCTAGTAAC[A/G]TGAAAAGGACCGATG | 51429 |
| rs117818468 | snp | C/G | 0.0165278 | 0.0893908 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821579 | TCAGAAATTTTCTAG[C/G]AATGTGTCACATATT | 51429 |
| rs117820471 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SNX9 | GRCh38.p7 | 6:157792438 | GCCACTGTGCCCAGC[C/T]GATTTTTTATTTTTT | 51429 |
| rs117845067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157935186 | TACCTCTGGGTAACC[A/G]GAATATTGATAAAGG | 51429 |
| rs117854061 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157872482 | CCTGAGCTGCACTGC[A/G]TGTGTCTGCAATCAC | 51429 |
| rs117854441 | snp | C/T | 0.133777 | 0.221342 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889166 | TCAGGCGCAGTGGCT[C/T]ACGCCTGTAATCCCA | 51429 |
| rs117861959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157772297 | TATGTTCAAGTCCTA[A/G]TGCCCAGTACCTGTG | 51429 |
| rs117865671 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | SNX9 | GRCh38.p7 | 6:157833984 | AGTCTGTCTCTCCAC[A/G]CTGGGGGCTACGTCA | 51429 |
| rs117877240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157758028 | AATTAAAAATTAGCC[A/G]GCCATGGTGGTGCAT | 51429 |
| rs117909075 | snp | G/T | 0.146314 | 0.227484 | intron-variant | SNX9 | GRCh38.p7 | 6:157866504 | GCTTGAGCCTGGTAG[G/T]TCGAGGCTGCATTGA | 51429 |
| rs117960778 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SNX9 | GRCh38.p7 | 6:157939475 | GCTGGTTATGGAGGG[A/G]AGATTGGAAGATGCA | 51429 |
| rs117975597 | snp | A/G | 0.34989 | 0.229177 | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157715552 | CTAGCCAGGGTGACA[A/G]AGTGAGACCCTGCCT | 51429 |
| rs117991452 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157721786 | TCCTGCTCTTTAGTG[A/C]GATGCAAGCGACCAG | 51429 |
| rs117993478 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, downstream-variant-500B | SNX9, LOC105378078 | GRCh38.p7 | 6:157884922 | GCATTGTTATACGTA[C/T]ATCCTGTCATCAGCA | 51429 |
| rs118017125 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157755626 | AGCTTGAATGTGAGA[G/T]ATTTAAAAGCAATGG | 51429 |
| rs118018445 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | SNX9 | GRCh38.p7 | 6:157741691 | TGCTTGAGGGACCCA[A/G]TGGCTCACTGGTAAA | 51429 |
| rs118023033 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157918520 | GTTTCTCTTATAGGC[A/G]AGATAGTTGGATCTT | 51429 |
| rs118043752 | snp | A/G | 0.0777841 | 0.181223 | intron-variant | SNX9 | GRCh38.p7 | 6:157804010 | TGACTACAGGTATAC[A/G]CCACCATGCCCGGCT | 51429 |
| rs118062421 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | SNX9 | GRCh38.p7 | 6:157859309 | TCTTTATGGAAATAC[A/T]GGCAAATATAAATAT | 51429 |
| rs118072414 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157837008 | GAACTTGGGTTCTGT[C/T]CTTGGTTGGTCCCTA | 51429 |
| rs118084588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157876405 | GCAGTAAGCCGAGAT[C/T]GTGCCACTGTACTCC | 51429 |
| rs118135398 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | SNX9 | GRCh38.p7 | 6:157803067 | AGGCCCCTTTAATAG[C/T]TTGACAACACTTCTC | 51429 |
| rs137859071 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157805394 | GCCTTCTCTACCATC[A/G]CTGACCATCCTTCAC | 51429 |
| rs137860641 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157839597 | AAAAATTATAATTTT[A/G]CTTTTCTGTAATAAT | 51429 |
| rs137894717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157793484 | TCTTTTTTGTTCCCT[C/T]CAACTAGTATCTTCT | 51429 |
| rs137907051 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SNX9 | GRCh38.p7 | 6:157742110 | TAATAGCACTGCTAA[C/T]TCGGAAATCTCTGCT | 51429 |
| rs137928309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157916983 | TTATATAGAATTGAT[A/G]CTGTTCTATAAGTGT | 51429 |
| rs137937937 | in-del | -/A | 0.0748431 | 0.178382 | intron-variant | SNX9 | GRCh38.p7 | 6:157847042 | GCAAGGCTCCATCTC[-/A]AAAAAAAAGATTATT | 51429 |
| rs137979606 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157730212 | AACTGTTTTTTTTTT[A/T]TTAAAAAAAAAAAAA | 51429 |
| rs138006655 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157875271 | TAGCTATTGCCATTC[C/T]CCAAAAGCAAAAACA | 51429 |
| rs138017295 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157903279 | AAACATAACATTTGA[C/G]ATATATTTAGACATC | 51429 |
| rs138026694 | in-del | -/TACTTTAATAA | 0.0551013 | 0.156571 | intron-variant | SNX9 | GRCh38.p7 | 6:157770409 | CACCCAAGTTTCATT[-/TACTTTAATAA]GTCAAACTAAAGAAA | 51429 |
| rs138074915 | in-del | -/C | 0.136166 | 0.22258 | intron-variant, upstream-variant-2KB, nc-transcript-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157892962 | CTGTGGCCCTCCGAG[-/C]CCCTCCATTTCACAG | 51429 |
| rs138077289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157921084 | TGGAAATACCATGTC[A/G]TTTGTAAGAATGACA | 51429 |
| rs138083816 | in-del | -/TA | 0.0279526 | 0.114869 | intron-variant | SNX9 | GRCh38.p7 | 6:157916973 | CTGGAAGAGATTATA[-/TA]GAATTGATACTGTTC | 51429 |
| rs138107076 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157774538 | CTGCGGTCATCGACC[C/G]ACGTGTCTGCCTTAG | 51429 |
| rs138110307 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157801780 | ATTGTGAGAAGAAGG[C/T]GGCTGTTGTGTCTGA | 51429 |
| rs138111727 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157878816 | AAATACTTCTGACTT[A/G]TGACGGATACAGGCT | 51429 |
| rs138120326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157864070 | GACTGGGTAACTTAT[A/G]AAGAACAGAATTTAT | 51429 |
| rs138147365 | snp | G/T | 9.89169e-05 | 0.00703197 | missense | SNX9 | GRCh38.p7 | 6:157875129 | CTTGATTCTCTCTCA[G/T]CCAGCACAGCTCAGG | 51429 |
| rs138150801 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157755250 | GCCCAGTAGGTCTCC[A/G]CCTCATTTTACCCAG | 51429 |
| rs138157201 | in-del | -/TTTG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157907279 | TGTTTTTTTGTTTGT[-/TTTG]TTGTTTGTTTTTAAG | 51429 |
| rs138162605 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822767 | AGGCGTGGGGCAAAG[A/G]CAGCGGGGTTGCGGG | 51429 |
| rs138173584 | in-del | -/TTCCTTTCTTTCCTTTCC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840434 | TTTTCTTTCTTTTCT[-/TTCCTTTCTTTCCTTTCC]TTCCTTTCTTTCCTT | 51429 |
| rs138188760 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157846645 | GATCATCTAGGCTGA[A/C]CCTGTCATTTTTCAT | 51429 |
| rs138191798 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | SNX9 | GRCh38.p7 | 6:157721243 | CCAAGATTGCGCCAC[C/T]GCACTGCAGCCTGGG | 51429 |
| rs138199544 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157851924 | GCTTATTTCAATTAG[C/G]GTAATGTTTTCAAGG | 51429 |
| rs138209355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157926655 | GGCATGGTGGCATGC[A/G]CCTAAAGTCCCAGCT | 51429 |
| rs138228778 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157775530 | TTGGTACCTCCACTC[A/C/T]GGTGGCCAACACCCC | 51429 |
| rs138229544 | snp | G/T | 0.0283406 | 0.115616 | intron-variant | SNX9 | GRCh38.p7 | 6:157739181 | CAGAATGGGAGAACA[G/T]TTTTGCAATGTATGC | 51429 |
| rs138234152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157850891 | CCATAGAAGGAAGGA[A/G]CATGCAGTTAGGATA | 51429 |
| rs138240053 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157809019 | AAACTGACTCAAAGT[A/T]AAAAAGGATGCAAAT | 51429 |
| rs138245224 | in-del | -/A | 0.0271762 | 0.113356 | intron-variant | SNX9 | GRCh38.p7 | 6:157733365 | GGTGCCTATAGTCCC[-/A]GCTACTCAGGTGGCT | 51429 |
| rs138246916 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157792503 | TATGTTGTTTTACTA[C/T]ATGTATACAATGTAG | 51429 |
| rs138249048 | snp | A/G | 4.97294e-05 | 0.0049862 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157906143 | ATTTCCTGGATTTGC[A/G]AAACCTGGCACGGAA | 51429 |
| rs138249361 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157868469 | CCTGGAGATTGGGTA[C/T]ATTTTGTTTCATAAA | 51429 |
| rs138277438 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157774273 | GAGGAGGTGGGGTAG[G/T]GGAGGAGGGATGTGG | 51429 |
| rs138292830 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157898510 | ACGTTTGTTTTAAAA[C/T]CTTGAGCCAGAAACG | 51429 |
| rs138293701 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SNX9 | GRCh38.p7 | 6:157729821 | TAATAGATTCTTCCA[A/G]TAAACTGAACATGAG | 51429 |
| rs138347702 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157780541 | ATCATAGAGTTGTCA[C/G]TTAAATTTTCCAGGA | 51429 |
| rs138354614 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157797725 | TAGAGAAAGGCTCAT[A/T]GAAGGACAGAAACAT | 51429 |
| rs138358094 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157855291 | ATACTTGATGAACTA[C/G]TCCTGCCTTTTAGGT | 51429 |
| rs138398289 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157883311 | ACCAAAAAAGTCCAC[A/G]TGACTCACTTTAACG | 51429 |
| rs138413041 | snp | C/T | 0.000158229 | 0.00889323 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157936010 | AGCAGGAAAGACTTA[C/T]GAAGAAATTGCCAGT | 51429 |
| rs138413908 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157736224 | GATGGGGATAGCATT[C/G]AAACTATAAATTACT | 51429 |
| rs138455652 | snp | A/G | 0.00716266 | 0.059414 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157944397 | AACAATGTTTATGCT[A/G]TAGCCATTTAATATA | 51429 |
| rs138471509 | snp | C/T | 0.00029985 | 0.0122407 | intron-variant | SNX9 | GRCh38.p7 | 6:157932171 | GCTCAGAAGACTAAT[C/T]GTTTATTCCTTTTTG | 51429 |
| rs138489262 | in-del | -/T | 0.00676609 | 0.0577691 | intron-variant | SNX9 | GRCh38.p7 | 6:157723543 | TTCTCAAGCTCTGGG[-/T]TTTTTCCCTCCCATG | 51429 |
| rs138491664 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SNX9 | GRCh38.p7 | 6:157829206 | TGAGAAATTGCCTGA[C/T]GTTTTAAGGTAGTTG | 51429 |
| rs138512031 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SNX9 | GRCh38.p7 | 6:157875980 | ACCCCATCTCCACAC[A/G]TTAAAAAAAAAGTTA | 51429 |
| rs138530742 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | SNX9 | GRCh38.p7 | 6:157902731 | GAAGTGCAGTGGTGC[A/G]ATCTTGGTTCACTGC | 51429 |
| rs138539100 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SNX9 | GRCh38.p7 | 6:157764226 | GCTCATGGTCATTGG[C/T]GTTCACATTGAAGTG | 51429 |
| rs138556209 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157910984 | CCGGTGTGGTGGTGT[A/G]CACCTGTAGTCTCAG | 51429 |
| rs138577802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157834025 | TTAGAGGTAATGAGG[C/T]GTGATCTGATTGGAT | 51429 |
| rs138577937 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157725720 | AATGTCAGAGATTAC[A/G]GATAGACGCAGATAA | 51429 |
| rs138600133 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SNX9 | GRCh38.p7 | 6:157779962 | TATTTCGTTTACTAA[C/T]AATGGGGCTGTTCGG | 51429 |
| rs138608406 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SNX9 | GRCh38.p7 | 6:157767050 | TTCTCCTCCTTGACC[C/T]AATGAATGTGAAAGC | 51429 |
| rs138622457 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | SNX9 | GRCh38.p7 | 6:157838535 | AGACCCTCTGACCTG[G/T]TTCCCTCCATTTAGC | 51429 |
| rs138643926 | in-del | -/TTTC/TTTCTTTCTTTCTTTC/TTTCTTTCTTTCTTTCTTTC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157780709 | GGACCTTCTTTTCTG[lengthTooLong]TTTCTTTCTTTCTTT | 51429 |
| rs138665340 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157746935 | GGGGTCAGAGGGTAT[A/G]AAACTGTTCCACCTC | 51429 |
| rs138669291 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157842122 | AAAAATTCAGAATAC[A/C]TTCTTAATATCTTCA | 51429 |
| rs138669685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157755125 | TGGTGAGATAGGGCC[A/G]GCTTCTTTACTGCAA | 51429 |
| rs138669767 | snp | A/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157715263 | TAAAGAATGTCAGTT[A/T]GGGCTGGGCACAGTG | 51429 |
| rs138677193 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157828720 | ACTGAGGTGATCCTT[C/T]CTCCTCAGCCCCGCA | 51429 |
| rs138684423 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157720548 | TGGGCTCATGAGACA[C/G]AAGCAAAGATTTGCT | 51429 |
| rs138687825 | snp | A/G | 1.6507e-05 | 0.00287284 | missense | SNX9 | GRCh38.p7 | 6:157902009 | AGCGAGGAAACAGTC[A/G]TGCTAGTTCCTCATC | 51429 |
| rs138711054 | in-del | -/A | 0.145305 | 0.227022 | intron-variant | SNX9 | GRCh38.p7 | 6:157939144 | TCAAGAAAAAAAAAA[-/A]GATGAATTTCTATAG | 51429 |
| rs138720593 | in-del | -/AT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157878431 | ATATGGAAGCCCACC[-/AT]TTTTTTTTTTTTTTT | 51429 |
| rs138733315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157941619 | CCAGCCTCCGCTGGC[A/G]GCCTTGCTGCCTACC | 51429 |
| rs138790027 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157925958 | GAGAGAAATGCTGAG[A/T]CCCCACATGGTGGAA | 51429 |
| rs138799017 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157930666 | AGCCCTTATGAGAAT[C/G]TAATGCCTGATAATC | 51429 |
| rs138855895 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SNX9 | GRCh38.p7 | 6:157859713 | ATTGAGCGTTTTGTC[A/G]TGCATTTAAGGGCCA | 51429 |
| rs138855966 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157847729 | TTCTGGTTTTAGTAG[C/T]GCTAAAATCCTGTAA | 51429 |
| rs138859861 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157935425 | GAGAACACAGGGACA[A/G]GGGAGTGTGTGACAT | 51429 |
| rs138870273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157834870 | AACAGTATGTAAAGC[A/G]TATTCAATGTCCTTG | 51429 |
| rs138876960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157936542 | TAAATGAATGCACTC[C/T]AGTATTGATGCCTCT | 51429 |
| rs138894063 | snp | A/G | 0.117537 | 0.212022 | intron-variant | SNX9 | GRCh38.p7 | 6:157730693 | CACCCAGGCTGGAGT[A/G]CAGTGGTGCAATCTC | 51429 |
| rs138907942 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157817653 | TCACGAGGTCAGGAG[C/T]TTGAGACCAGCCTCG | 51429 |
| rs138910075 | in-del | -/TGA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157897193 | GTGTCCTACAGTCAT[-/TGA]GACACTGTCTACCTG | 51429 |
| rs138943171 | in-del | -/ATTA | 0.0279526 | 0.114869 | intron-variant | SNX9 | GRCh38.p7 | 6:157896715 | TTTGAATACATTTCT[-/ATTA]ATTGTTTTTAGTACT | 51429 |
| rs138964893 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157813436 | CAGGAGGTAGAGGGT[A/G]TGGGGGCGGCAGCTC | 51429 |
| rs138966319 | in-del | -/C | 0.0607341 | 0.163335 | intron-variant | SNX9 | GRCh38.p7 | 6:157854627 | CTTTTAGAAACTGTT[-/C]CTTTTTAACTTCATT | 51429 |
| rs138966546 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157766218 | TCCCCCATTTCAAAG[C/G]GATGAACTTGTCACA | 51429 |
| rs138997881 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157865351 | TCAGGAAAAAAAAAA[A/C]AAAAAAAACACCACA | 51429 |
| rs139023190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157758940 | TGAGTTCAACAGGGA[A/G]ACCTGAACTGAAGGC | 51429 |
| rs139048593 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SNX9 | GRCh38.p7 | 6:157731226 | CTCAAAACTCCTGAC[C/T]TCGTGATCCACGTGC | 51429 |
| rs139048740 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157756311 | CCAAGTACTTGGGGG[A/G]CTGAGGCAGGAGGAT | 51429 |
| rs139050626 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157790215 | CCTGGGGGAATTCCA[C/T]TTCCTGTAAGGAGAA | 51429 |
| rs139055876 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157942009 | AATAATGCAAGGGCA[A/G]CTCTCAAAATTTTGA | 51429 |
| rs139079583 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157826245 | GTCTCACGCCTGTAA[C/T]CCTAGCACTTTGGGA | 51429 |
| rs139090397 | snp | A/G | 0.0144894 | 0.0838733 | intron-variant | SNX9 | GRCh38.p7 | 6:157928738 | GCACTGGGCTCGTAG[A/G]GGGTGATGCAGGCTC | 51429 |
| rs139096541 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | SNX9, LOC105378078 | GRCh38.p7 | 6:157884857 | AAACAAACTATTAAA[A/G]CAAAGTCTTTTTTTT | 51429 |
| rs139108733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157723608 | TTTCTTCAGGCTCCA[A/G]GAAAACCAACCTCAC | 51429 |
| rs139123639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157795298 | TAGTGTGCCTGTAGT[C/T]CCAGCTACTCGAGAA | 51429 |
| rs139133972 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | SNX9 | GRCh38.p7 | 6:157869574 | CCTCTTCTCTCCACC[C/G]TGCGCTTCCTGCCAG | 51429 |
| rs139190300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157763184 | GTATAGGTGGCCACC[A/G]TCCCAGGTGGGCTCC | 51429 |
| rs139210159 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157769732 | TGGAGGCCTGTGTGG[-/A]GGATTTTTGGTGGAG | 51429 |
| rs139235501 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157799378 | AAGAGGATTAAATCA[A/G]TTACTCTCACCCAGT | 51429 |
| rs139268255 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157788512 | ACAACTCAGAAAAAT[A/C]AAAATTCTAAAAAGA | 51429 |
| rs139324771 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SNX9 | GRCh38.p7 | 6:157864590 | GGACCAATAACACAA[C/T]AGCAGGTTCCTCATG | 51429 |
| rs139376954 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157755858 | GACTTTGATCTTCTC[A/G]GACATTGCTGGAGAG | 51429 |
| rs139384413 | in-del | -/TAAT | 0.0349115 | 0.127424 | intron-variant | SNX9 | GRCh38.p7 | 6:157935003 | AGTGAAAATAATAAT[-/TAAT]GTGGAATGAAGCATA | 51429 |
| rs139387159 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157792244 | CCTCCCGGGTTCAAG[C/T]GATTCTCCTGCCTCC | 51429 |
| rs139396234 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157831324 | ATTTGTGTGTGCTGA[C/T]ACCAGTCTCCTGGGG | 51429 |
| rs139400468 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SNX9 | GRCh38.p7 | 6:157904626 | TGAGGCAGGATAATC[A/G]CTTGAACCAGGAGGT | 51429 |
| rs139403857 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157857146 | CTCATGAGTTTAAGC[A/C]AATTTAATGTTTCAG | 51429 |
| rs139404985 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157737289 | CTGGTCCTCATTTTT[-/T]TTTTTTGGTTGGTAG | 51429 |
| rs139412308 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | SNX9 | GRCh38.p7 | 6:157844035 | CCATACCTCCTCACC[A/T]GCCTAATTTTTGTAT | 51429 |
| rs139414336 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157919101 | CTTTAGTAATTTCTT[G/T]TTAGCCTGAAGGACT | 51429 |
| rs139426788 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SNX9 | GRCh38.p7 | 6:157748626 | CCCAGCTACTTGAGA[A/G]GCTGAGGCAAGAGAA | 51429 |
| rs139443547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157759520 | GCCAATATGGTGAAA[C/T]CCTGTCTCTAGTAAA | 51429 |
| rs139447316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157903777 | CTTAAGGCAAGTTTC[A/G]TGACCTGTTGGAACC | 51429 |
| rs139457269 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157728434 | TCAGCTGCCTTAAAC[A/T]TGTGTCAGAAATCGA | 51429 |
| rs139459055 | snp | A/G | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157835944 | TTTATTTTTTATTTT[A/G]GTTGAGAAGGGTCTC | 51429 |
| rs139459972 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157786168 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 51429 |
| rs139462389 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | SNX9 | GRCh38.p7 | 6:157772804 | GAGCCCAAGTAAGGA[C/G]CCTCAATATGGGAAA | 51429 |
| rs139504884 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157785908 | ATTCCTCATGCAGCA[C/T]AGCAGTCTAGAATGC | 51429 |
| rs139550825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157836400 | AGATATGGCAATGGT[A/G]ATAAGCTTCCATCTG | 51429 |
| rs139551393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157900031 | CATGCTGTACATGAG[A/G]TCTCTAGACTTATCC | 51429 |
| rs139551399 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157853750 | AAAGAGGAAATAGTT[A/G]TGCCACAATTTTTAG | 51429 |
| rs139577430 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157731567 | TTAAGAAGATGTTTG[C/T]TCTCTGAATGAGTTA | 51429 |
| rs139610116 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SNX9 | GRCh38.p7 | 6:157781632 | CTAGGGAGTGAGCAG[A/G]AGCAGGTAGAAACCG | 51429 |
| rs139610537 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157790637 | GTCCTTGGGAGGATT[C/G]AACTGGGAAGCTCTG | 51429 |
| rs139624210 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | SNX9 | GRCh38.p7 | 6:157735092 | GCTTGGGAAATATGG[C/T]GAAACACCGTCTCTA | 51429 |
| rs139629611 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SNX9 | GRCh38.p7 | 6:157842571 | TTTTTAAAGATAATT[C/T]GGTGTTTTTAAAGAT | 51429 |
| rs139632031 | snp | A/G | 0.00148424 | 0.0272014 | missense | SNX9 | GRCh38.p7 | 6:157942822 | GGCAGGCCCTCAGCC[A/G]CTTTCCAGTGATGTA | 51429 |
| rs139639191 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157744225 | CAGTTTAGTGGCTGA[A/G]TAGCTGAGTTGTAGA | 51429 |
| rs139679306 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SNX9 | GRCh38.p7 | 6:157840262 | GCTTGCACAGTGAGG[C/T]CAGAGCTGAGGGAGC | 51429 |
| rs139754357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157884519 | TAATGCCTTAGACAT[C/T]TCGTAATTGCTTATT | 51429 |
| rs139779957 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | SNX9 | GRCh38.p7 | 6:157770765 | GAGATCGCGCCACTG[C/T]ACTCCAGCCTGGGTG | 51429 |
| rs139785802 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157815298 | GCTCACTGCAGCCTC[A/G]GATTCCTGGGCTCAA | 51429 |
| rs139792701 | snp | A/G/T | 0.00398691 | 0.0444912 | intron-variant | SNX9 | GRCh38.p7 | 6:157762920 | TCTCCCTGGTGGAAG[A/G/T]GGGACAGGACACCTT | 51429 |
| rs139796066 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157830424 | AGTTAGCTAATTATT[G/T]TTCCTTTGTCCGTGG | 51429 |
| rs139808703 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157772559 | AGGTGAGGACGAATC[C/T]TTCCCCAGAGCCTCT | 51429 |
| rs139841192 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | SNX9 | GRCh38.p7 | 6:157877611 | TCATTTTCTGAATGC[A/G]GGTAGGAAGATGTGT | 51429 |
| rs139892755 | in-del | -/TGTG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157734218 | TCAGTTTAGGATTTA[-/TGTG]TGTGTGTGTGTGTGT | 51429 |
| rs139918257 | in-del | -/CCTGTAAGACCACCTGG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157724022 | AGTTGGGGGCTCGGC[-/CCTGTAAGACCACCTGG]CCTGTAAGACCACCT | 51429 |
| rs139933337 | in-del | -/AAAAG | 0.0283406 | 0.115616 | intron-variant | SNX9 | GRCh38.p7 | 6:157933300 | CCCCATCTCAAGAAA[-/AAAAG]AAGAAAAAGCATTTG | 51429 |
| rs139959862 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157880603 | GTTACTTCTTTCTGT[G/T]CCCTCTTTTTATTCT | 51429 |
| rs139964124 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157819408 | TGCACTCCTTTCCAC[A/G]TTTATTTTCAAGGTC | 51429 |
| rs139968305 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157866507 | TGAGCCTGGTAGGTC[A/G]AGGCTGCATTGACCC | 51429 |
| rs139969704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894593 | GATTGGGTGCCATCT[A/G]TTTCCCATTCCAAAA | 51429 |
| rs139974183 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SNX9 | GRCh38.p7 | 6:157869171 | TCCCCGGCCTCACTG[A/G]CTGTCCTCTTGTGTC | 51429 |
| rs139997124 | snp | A/C/T | 0.00835141 | 0.0640778 | intron-variant | SNX9 | GRCh38.p7 | 6:157757042 | TCCACCCCCTCCCCC[A/C/T]ACCAGGAGCTGGCAG | 51429 |
| rs139997599 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157880836 | GATCTCACACATCCT[A/G]TGTGAATCAGGGTAA | 51429 |
| rs140002699 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SNX9 | GRCh38.p7 | 6:157809571 | TGGGGAAAATATTTA[C/T]AAAACAAATATCTGA | 51429 |
| rs140002918 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SNX9 | GRCh38.p7 | 6:157744373 | AGTACATCATGCAAT[C/T]TCCAGGTATAATCTT | 51429 |
| rs140013763 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157718176 | CCACTTTTTAATCCA[A/G]TCATCTGGTGATGGG | 51429 |
| rs140028974 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SNX9 | GRCh38.p7 | 6:157768438 | CTTACTTTTACATAA[A/G]TGTTTTTAGAAGCAG | 51429 |
| rs140034286 | in-del | -/CAG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157736003 | GAGCCTCTCAATGAT[-/CAG]TCACTGAAGATGTTT | 51429 |
| rs140038679 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157718446 | GGGGTCCTCTTTGAG[C/G]TCAGATCCTATATCC | 51429 |
| rs140040840 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | SNX9 | GRCh38.p7 | 6:157824921 | TTACCAGTTACACAT[C/G]CTAGTACATGCTCAT | 51429 |
| rs140041852 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | SNX9, LOC107986663 | GRCh38.p7 | 6:157714537 | GCCCTAGGATGACCA[C/T]GGGAATTTATCCCTT | 51429 |
| rs140081720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157905144 | GCCATCCAGCTGCAG[A/G]ACACATCTGGTCTCT | 51429 |
| rs140101958 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | SNX9 | GRCh38.p7 | 6:157781272 | AGAGCAGGCTCTGCC[G/T]TCTGGCTCCTTCACC | 51429 |
| rs140106173 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157722551 | GCCTCCACAGCCATT[C/T]TGCTCCAGCCTACAG | 51429 |
| rs140172024 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157848775 | CGATAGTACAGCAGC[C/T]GTAAAATGATAGGGG | 51429 |
| rs140180354 | snp | A/G/T | 0.00597247 | 0.0543191 | intron-variant | SNX9 | GRCh38.p7 | 6:157923104 | CAAAGAGGGATCAAC[A/G/T]TGTCATAAAAGTGGT | 51429 |
| rs140187140 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157927447 | AAGCCAGTGATTTCA[C/T]AGTTGACACGGTGCT | 51429 |
| rs140202981 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157811048 | GCACTTCAGCGAGAC[C/T]CTGTCACCAAAACAA | 51429 |
| rs140204509 | snp | A/G/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157852355 | GTCTGATTACTGGAC[A/G/T]TCAAAAGCTGCTTTG | 51429 |
| rs140212807 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157916280 | ACCTCATGATTCACC[C/T]GCCTCGGCCTCCCAA | 51429 |
| rs140237474 | in-del | -/ACACAC | 0.0279526 | 0.114869 | intron-variant | SNX9 | GRCh38.p7 | 6:157927931 | AAGTATAGACAAGTA[-/ACACAC]ACACACACACACACA | 51429 |
| rs140266584 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SNX9 | GRCh38.p7 | 6:157858514 | AGTGTGAGCCACCAT[A/G]CCCGGCCATTGTCCA | 51429 |
| rs140293474 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157841627 | TGGGGAGGTGGTTGC[C/T]AGGAGGAAGTTGTCT | 51429 |
| rs140317802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157720712 | AGGGTTGTGAAGACA[C/T]CTCACAGCCCATTAC | 51429 |
| rs140321974 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157780114 | GGACCCCAAGGTCCC[A/G]CCTGGCTCTCCTGCC | 51429 |
| rs140324494 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SNX9 | GRCh38.p7 | 6:157933326 | AAGCATTTGTCAGCT[A/G]GGTGGCACCTATTAA | 51429 |
| rs140326668 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157927113 | TTCTCATTTACAGGA[A/G]TGGAAAACTGGAAAG | 51429 |
| rs140329086 | in-del | -/G | 0.127254 | 0.217792 | intron-variant | SNX9 | GRCh38.p7 | 6:157931286 | CTGAGCTCGTGTAAT[-/G]TTGGATTCATGTTTC | 51429 |
| rs140340603 | in-del | -/T | 0.0170251 | 0.090679 | intron-variant | SNX9 | GRCh38.p7 | 6:157876585 | CTCAGATATTTAAAA[-/T]TTTGCAGGCAAGGTG | 51429 |
| rs140350458 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | SNX9 | GRCh38.p7 | 6:157724562 | TACTGTCTTGTACCT[A/G]ACTTCAACCAGATGG | 51429 |
| rs140354004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157934542 | TATGCCCCCAGGAGC[A/G]GGTGCCTCAAGGTCA | 51429 |
| rs140354558 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SNX9 | GRCh38.p7 | 6:157900866 | TCCGTAGAAACAGGA[C/T]GTGAAGCTAGACAAC | 51429 |
| rs140382504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157783120 | AAAACTGGGGTGGCT[A/G]TATTACTTTTGGAGA | 51429 |
| rs140394385 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157817108 | ATCTGCTGGTGCCTT[C/G]ATGTTGGACTTTTCA | 51429 |
| rs140399713 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157937590 | ATGTGCGCAGTAGTC[A/G]GTATTGGTTTTATAT | 51429 |
| rs140406341 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157920653 | GCACTCATTTGGTTG[C/T]TTTTATTACTGTTGT | 51429 |
| rs140414715 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | SNX9 | GRCh38.p7 | 6:157752123 | TGGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 51429 |
| rs140420661 | snp | A/G/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157737602 | TCTTTTCAAAAAACC[A/G/T]GCTCCTGAGTTCATT | 51429 |
| rs140456992 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157764915 | AGTATAATTACAGAT[A/C]CCTGTGCTCTGAGGG | 51429 |
| rs140463888 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157905421 | GTCTTTTTCAGTAGC[A/C]CTTTGGATGGCTATG | 51429 |
| rs140464233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157802052 | AGAAACTTGGCCAAT[A/G]GGAATATTCTCAGAG | 51429 |
| rs140489029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157787593 | AGAAAAGCTCAGGGC[A/G]TCATTATGTCATAAT | 51429 |
| rs140498104 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157863494 | TAGTTGTGGTTGACA[A/G]TATATATTGAATATA | 51429 |
| rs140516788 | snp | C/T | 4.95471e-05 | 0.00497705 | missense | SNX9 | GRCh38.p7 | 6:157867596 | GAAATAATGAACTGA[C/T]GGTTAATGAAGGAGA | 51429 |
| rs140521035 | snp | A/C | 0.0569829 | 0.158885 | intron-variant | SNX9 | GRCh38.p7 | 6:157755141 | GCTTCTTTACTGCAA[A/C]CTGCTTTATCAGCAA | 51429 |
| rs140521641 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SNX9 | GRCh38.p7 | 6:157767964 | GGACAGCTGGGCCAT[A/G]TCTGCTGCCTCACAG | 51429 |
| rs140527110 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157740714 | GAAAAGAGCTCACAA[C/G]TGCCATTGGTTTCCC | 51429 |
| rs140551137 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157935434 | GGGACAGGGGAGTGT[G/T]TGACATATCACCAGA | 51429 |
| rs140563665 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157940398 | ATTTACTGGAAAGTA[A/G]TGTTTGTCATTAGCT | 51429 |
| rs140565976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157838158 | GCTGGGACTACAGGC[A/G]TGCATCACCATGCCT | 51429 |
| rs140568433 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SNX9 | GRCh38.p7 | 6:157910917 | ACGAGGTCAGGAGAT[C/T]GAGACCATCCAGGCT | 51429 |
| rs140599646 | snp | A/G | 0.210909 | 0.246925 | intron-variant | SNX9 | GRCh38.p7 | 6:157792333 | TCTAGTAGAGATGGC[A/G]TTTCACCATGTTGGC | 51429 |
| rs140616711 | snp | C/G | 0.0275645 | 0.114116 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822571 | CAGAATGAGGTTAAC[C/G]GGGCGTCACAGAACG | 51429 |
| rs140617803 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SNX9 | GRCh38.p7 | 6:157898378 | GGCCCCTGCTGTCGC[C/T]CGTGGATCACTGCAT | 51429 |
| rs140636960 | in-del | -/TC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157813902 | CTCTCTCTCTCTCTC[-/TC]CTGATTTTTTAGAAG | 51429 |
| rs140650829 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SNX9 | GRCh38.p7 | 6:157766348 | AAGAAATCTTTCCTA[C/T]TGCTGGACTCAAAAT | 51429 |
| rs140680533 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | SNX9 | GRCh38.p7 | 6:157881567 | CCTCTTGAGCCAAAC[A/C]CTTAGCCAAGTTGTG | 51429 |
| rs140706364 | in-del | -/CT | 0.00874735 | 0.0655527 | intron-variant | SNX9 | GRCh38.p7 | 6:157870319 | ACGCACACACACCTA[-/CT]CTCTCACCTGCGCTC | 51429 |
| rs140710394 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157769658 | CACCAAGGCCGGAGA[A/C]GGCCTGGCTGGAGCT | 51429 |
| rs140738771 | snp | G/T | 0.0356815 | 0.128715 | intron-variant | SNX9 | GRCh38.p7 | 6:157915767 | GAGGCGGAGGTTGCC[G/T]TGAGCCAAGATTGCA | 51429 |
| rs140745027 | in-del | -/T | 0.0252325 | 0.109451 | intron-variant | SNX9 | GRCh38.p7 | 6:157718254 | GACAGTCCAGGTGTC[-/T]TTTTTTATATAATGA | 51429 |
| rs140757739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157723971 | TGCTGATAACTTCTG[A/G]AGTAAGCACAGACCC | 51429 |
| rs140767756 | snp | C/T | 9.89642e-05 | 0.00703365 | missense | SNX9 | GRCh38.p7 | 6:157875151 | CAGCTCAGGCCAGTT[C/T]GTCGGCTGCCAGCAA | 51429 |
| rs140777792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157848883 | GGTGACATCTAAGCT[A/G]AGACCTGAAAGGTGA | 51429 |
| rs140798179 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157773635 | AAGGATGTCAGTTAG[G/T]GAGCTTTGGCTGCCG | 51429 |
| rs140803873 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | SNX9 | GRCh38.p7 | 6:157919046 | AAATAAGCAGCACCG[A/C]AAATATAAGGATTAA | 51429 |
| rs140844034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157917328 | TTTATCATTTCTATC[A/G]CTTGGTTTGGGTTTG | 51429 |
| rs140849616 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SNX9 | GRCh38.p7 | 6:157939366 | GAAATAAATTTTGAT[C/T]GTGAAGGAACTTGAA | 51429 |
| rs140858108 | in-del | -/CA | 0.0573587 | 0.15934 | intron-variant | SNX9 | GRCh38.p7 | 6:157869852 | CATTATGCATACCCC[-/CA]CACACACTCGCACAC | 51429 |
| rs140858172 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SNX9 | GRCh38.p7 | 6:157920490 | CCACCATGTCGAACA[C/T]GTGGGGTGGGTGGCA | 51429 |
| rs140867459 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SNX9 | GRCh38.p7 | 6:157799070 | GGGGAAGGGGAAGCA[A/G]GCACCTTCTTCACAA | 51429 |
| rs140879280 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821261 | TGCATAGGATTTGCC[A/G]GATGAGCATGTGGAA | 51429 |
| rs140881573 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SNX9 | GRCh38.p7 | 6:157749700 | TATTTTTAGTAAAGA[C/T]GGGGTTTCACCATGT | 51429 |
| rs140881822 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157785437 | GAAATAATAGATCAC[G/T]ACCAAGTGGGGTTTA | 51429 |
| rs140882271 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157898293 | TACTTATCTGTGTGA[A/T]GTCACAGATTCAAAC | 51429 |
| rs140886408 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157779682 | CAAAATGGGTACAGT[C/G]AGTACACAGAGACTT | 51429 |
| rs140904940 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SNX9 | GRCh38.p7 | 6:157800455 | CCAATCTGGGCAACA[C/T]GGCAAAACTGTCTCT | 51429 |
| rs140907945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157720277 | GGTGTTGTACACTTT[A/G]TTGATTGCAACTAGA | 51429 |
| rs140908018 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157765346 | TATTTGTTTTTTTTT[-/T]GTTTGTTTGTTTGTT | 51429 |
| rs140911881 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157769016 | CTGCACTCCAGCCTG[G/T]ACGACAGAGCAAGAC | 51429 |
| rs140923818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157878168 | GAGTTGCTGGTGTCA[A/G]GGCAGTGTTGCTGCA | 51429 |
| rs140952755 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157866957 | GTGTTTGTTTGTTTG[G/T]TTTTTTAAGAGACTG | 51429 |
| rs140954846 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157942999 | AGCCACCCTAAATGC[A/G]TCAGTTATTTAGGGA | 51429 |
| rs140969244 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157930132 | TACCTCAACCATTGG[C/G]CAATAACTACCTCTG | 51429 |
| rs140971754 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157786603 | CTCAGGATACAAGGT[C/T]AATATGTAACAATCA | 51429 |
| rs140977180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157758460 | GAATGGATTCGAGAG[C/T]GGCAAGTCTGGGGAT | 51429 |
| rs141010835 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SNX9 | GRCh38.p7 | 6:157724988 | GATAATTCAGGTCTG[C/T]GGGTGATAAATTCTT | 51429 |
| rs141028089 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157771510 | ATTCAATAACTTGTA[G/T]TTTTAAAAATAGTAT | 51429 |
| rs141028798 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157796323 | GACCAGAGAAGAGAG[A/G]TGTGAGTCAGGACAG | 51429 |
| rs141036834 | snp | C/T | 0.000280064 | 0.0118302 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157909910 | CCTTATTTTGTAGAA[C/T]ACTAATCGATCTGTA | 51429 |
| rs141041523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157862708 | TTCCTTCCTATTTTG[A/G]ACTGTTTTATTCTCT | 51429 |
| rs141058424 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157874663 | GAACATTCTCTAAGA[C/T]AGACCACATATTCTG | 51429 |
| rs141086561 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157763837 | GAATCAGCCTCATGA[C/T]GTTTCCAGTGTGTTA | 51429 |
| rs141096310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157774033 | AGCGTCTGGACTGAA[C/T]AGACGAGAGCCAACT | 51429 |
| rs141099319 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | SNX9 | GRCh38.p7 | 6:157754932 | GGGCTGCTGGTTGCC[C/T]ATTTTTATGGTTGTT | 51429 |
| rs141137818 | in-del | -/TTTG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157907278 | CCTCAGTTTTGTTTT[-/TTTG]TTTGTTTGTTTGTTT | 51429 |
| rs141146899 | snp | A/G | 4.94597e-05 | 0.00497266 | missense | SNX9 | GRCh38.p7 | 6:157932225 | ATCAGAAGATAGGAA[A/G]GGCCTTGCAGAGTTT | 51429 |
| rs141158329 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157849184 | AAGTGATAAGGCCAC[A/G]GAGGTGTTCAGGGTC | 51429 |
| rs141167056 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157801205 | TACTGTTTCTACAGA[C/T]GGGCTTCTGATCTTC | 51429 |
| rs141177156 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SNX9 | GRCh38.p7 | 6:157865067 | TACCGCAGCCAGGCA[C/T]GGTGGCTCACGCCTG | 51429 |
| rs141202434 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | SNX9 | GRCh38.p7 | 6:157789626 | TGTGTGACCTTAAGC[A/G]AGTTATGTAATATCA | 51429 |
| rs141205393 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157756213 | AGGTCAGGAGTTCAA[A/G]ACCAGCCTGGGCAAC | 51429 |
| rs141215424 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157778611 | GATCATCTACTCTGC[A/G]TTAGACACTGTGCTG | 51429 |
| rs141215607 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | SNX9 | GRCh38.p7 | 6:157741218 | TCAGGTGTGGTGGCA[C/T]GCACCTGTAATCCCA | 51429 |
| rs141269183 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157908754 | CAAAACTTACACGAG[A/G]TCTCTACACCCCCAC | 51429 |
| rs141276175 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157839913 | AAAGCTCAGACCTTT[C/G]TGTCTTAATGTGATA | 51429 |
| rs141281371 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157745625 | GAAAGTTTGGCATTT[C/T]CATTCTGCCCAGGGT | 51429 |
| rs141294599 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157914042 | TTTGGCAAGTATATA[G/T]TTAATGTTTAAGAAA | 51429 |
| rs141302274 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | SNX9 | GRCh38.p7 | 6:157859488 | TATTTAATCAGTTGC[C/G]TGTTAGTAGAAGCTA | 51429 |
| rs141303282 | snp | A/C | 0.0482946 | 0.147699 | intron-variant | SNX9 | GRCh38.p7 | 6:157783905 | GCCTCAGCTTCCCAG[A/C]GTGCTGGGATTACAG | 51429 |
| rs141335368 | snp | G/T | 0.0429648 | 0.14013 | intron-variant | SNX9 | GRCh38.p7 | 6:157844596 | ATCCTTGTTTTTTTT[G/T]TTTGTTTTTTTTTTT | 51429 |
| rs141342551 | in-del | -/CT | 0.029116 | 0.117091 | intron-variant | SNX9 | GRCh38.p7 | 6:157870253 | AGACACTCTCACCTG[-/CT]CTCTCACATCCCCAC | 51429 |
| rs141391214 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885656 | GATGACATCATCACA[A/G]GTGGTGTGGAAGGAT | 51429 |
| rs141410672 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157737742 | TCTTTTAATTGTGAC[A/G]TTAGGGTGTTGATTT | 51429 |
| rs141458010 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157845963 | ATCAGAGGTGCTTTT[A/G]TAACACTTTCAGTGT | 51429 |
| rs141497096 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157764227 | CTCATGGTCATTGGC[A/G]TTCACATTGAAGTGG | 51429 |
| rs141525968 | in-del | -/TT | 0.26078 | 0.249767 | intron-variant | SNX9 | GRCh38.p7 | 6:157858251 | TCTTTTTCTTTTTTC[-/TT]TTTTTTTTTTTGAGA | 51429 |
| rs141550181 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157899275 | TTGCCCTTCTCTCCC[C/G]TTTATTGTTAGTGTT | 51429 |
| rs141567144 | snp | A/C/T | 0.0047834 | 0.0487097 | intron-variant | SNX9 | GRCh38.p7 | 6:157835577 | TCGTGTCCCCACCCA[A/C/T]ATCTCATCTTGAATT | 51429 |
| rs141568616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157732922 | AACCACAATTCTACT[C/T]TCTGCTGCTGTTTGA | 51429 |
| rs141577914 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157780807 | CTGGCAAACCTAGGG[A/G]TCCACAGTGTTGTGT | 51429 |
| rs141610538 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157770145 | CTAATGGTACGTGGA[C/G]TCCATCCAAGGCCTC | 51429 |
| rs141628632 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157767208 | TAACTCCCCTGCTCT[A/G]AGCGGTTGAGCTAGC | 51429 |
| rs141631672 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157729537 | AGAGCGCTGACATAT[A/C]TAATAGAATGTAGAA | 51429 |
| rs141632724 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157838875 | AACCAGTGAACATTC[C/G]AGGCAAGTAGTCTGT | 51429 |
| rs141642941 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157841984 | TTTCCTCTAGCCTCC[C/T]CTCCCCTATTTTCCC | 51429 |
| rs141645428 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | SNX9 | GRCh38.p7 | 6:157733276 | CGAGGTCAGGAGATC[A/G]AGACCATCCTGGCAA | 51429 |
| rs141656005 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157944971 | TCACATGCACCATTT[A/G]GTTCTTAGATACGTT | 51429 |
| rs141658868 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157830030 | CTGAATTACAAAAAG[A/G]CATAAGGTTATTTAA | 51429 |
| rs141662189 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157903462 | ATGCATAATAAAGTG[A/C]ATAATTCTCTGTCTT | 51429 |
| rs141696467 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157732252 | AGAGCCATTCTCACA[G/T]CACTCCACGCCTTCT | 51429 |
| rs141718751 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157772382 | TCTTGCTGGAATAGA[A/C]CCCAAGTGGGCCCTA | 51429 |
| rs141754703 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157876566 | ATTCTGAATTACAAA[C/T]TAGACTCAGATATTT | 51429 |
| rs141810933 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | SNX9 | GRCh38.p7 | 6:157869400 | ACACTGACCACGTCC[A/C]GACTCAGCTCATCAC | 51429 |
| rs141825896 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | SNX9 | GRCh38.p7 | 6:157717113 | GTCTTGCTCTGTCAC[C/T]GAGGCTGGAGTGCAG | 51429 |
| rs141851391 | snp | A/G | 0.00041965 | 0.0144793 | intron-variant | SNX9 | GRCh38.p7 | 6:157867653 | GAGAACTGTACATTC[A/G]AGTCTGATTGTCCCA | 51429 |
| rs141867592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157828723 | GAGGTGATCCTTCCT[C/T]CTCAGCCCCGCAAAG | 51429 |
| rs141876827 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157876040 | CTTACATCTTTAGAA[A/G]TGAATGGGCTTTAGG | 51429 |
| rs141896100 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157814339 | AAACATGGTCTAGCC[A/G]ATGTCAGGGAAATGC | 51429 |
| rs141903501 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887822 | TCACAGGAGAGTTGC[A/G]CCTGAAAAGGATGCT | 51429 |
| rs141906900 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157737284 | TCCGTCTGGTCCTCA[-/T]TTTTTTTTTTGGTTG | 51429 |
| rs141930762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157746379 | AAAAAAACATTAAAA[C/T]GTAAGTGTATGAAAC | 51429 |
| rs141932984 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157811795 | ATGATCTAGTGCCAC[C/G]AAACAAATTACTCCA | 51429 |
| rs141939312 | in-del | -/TGTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157866942 | TGTTAATGAAATAGG[-/TGTT]TGTTTGTTTGTTTGT | 51429 |
| rs141974380 | snp | C/G | 0.0283406 | 0.115616 | intron-variant | SNX9 | GRCh38.p7 | 6:157860341 | AGCCCAGGAGTTCAA[C/G]GCTGCAGTGAGCCAT | 51429 |
| rs141976519 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157936265 | GGCACAGTGGCTCAC[A/G]CCTGTAATCTGGCAC | 51429 |
| rs141987950 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | SNX9 | GRCh38.p7 | 6:157815282 | CAGTGGCCTGATCTT[A/G]GCTCACTGCAGCCTC | 51429 |
| rs141995188 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894074 | TTCAGCTGGATCCCT[A/G]TATCATTTCTTTTTC | 51429 |
| rs142015242 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157753162 | AAGTAACAGTCTGAT[C/T]TCTCTTTCTTTTCTC | 51429 |
| rs142017401 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | SNX9 | GRCh38.p7 | 6:157818616 | GTCTCCAAGGACTCA[C/T]GCCAGCCTGTCCTTA | 51429 |
| rs142041159 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157817730 | AAAATACAAAAATTA[G/T]CTGGGCATGGTGGCA | 51429 |
| rs142044364 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157750861 | AACGGGCATATGGAA[A/G]GATGTTCAATGCCAC | 51429 |
| rs142074649 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | SNX9 | GRCh38.p7 | 6:157751090 | CACTGCTGATAAAGA[C/T]GTACCCAAGACTGGG | 51429 |
| rs142084257 | snp | A/G | | | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157715281 | GCTGGGCACAGTGAC[A/G]CATGCCTGTAATCCC | 51429 |
| rs142174818 | in-del | -/ATTA | 0.264906 | 0.249555 | intron-variant | SNX9 | GRCh38.p7 | 6:157875398 | GAGAAAAGGCAGGGT[-/ATTA]TATTGAGGGTTGCTT | 51429 |
| rs142200157 | snp | C/G | 0.127254 | 0.217792 | intron-variant | SNX9 | GRCh38.p7 | 6:157900532 | TCCGGGGGGGTCACT[C/G]CCTTCTGGTCCTGCA | 51429 |
| rs142217663 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157795125 | ATGAAATATAAAAAC[A/G]CATCTTGAGGCGGGG | 51429 |
| rs142218371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157734731 | CGTTATGGGTACAGC[A/G]CATGTCAGTAGACTT | 51429 |
| rs142227731 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157782471 | ATCAAGCTGTACAAT[A/G]TTACCTCTAAGTGGA | 51429 |
| rs142271394 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SNX9 | GRCh38.p7 | 6:157850982 | GTGATAAGGCTGGGC[A/G]TGGTGGCTCATGCCT | 51429 |
| rs142285018 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157854421 | GAGAAAATATGAATA[A/C]ATAAAAGTCCTAAAT | 51429 |
| rs142285120 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157806301 | ATTTCTGCATGTGCC[A/G]TAGGTTACTGAGTTG | 51429 |
| rs142288579 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SNX9 | GRCh38.p7 | 6:157929427 | AATGCTGCGACTGCA[C/T]TGCTGTCCCATGCGC | 51429 |
| rs142294484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157843651 | ATTTTAACTTAAAAT[A/G]TATAATGTGCATTTA | 51429 |
| rs142304462 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SNX9 | GRCh38.p7 | 6:157833139 | TCCTAATTTAAATTC[A/G]CAGAAAAAGGCTTGA | 51429 |
| rs142316779 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157905172 | TCTTGTGTAAGCTGC[A/G]TTTTAAAGGAATGTC | 51429 |
| rs142329038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157791888 | ATTTAACAAGAGGTT[C/T]AGAAAAAATAATCCA | 51429 |
| rs142392121 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890435 | ATTTCTCTATTTGCA[G/T]TATGAGGAGAGGATA | 51429 |
| rs142405844 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157877841 | TAGCATCAGTAAGTT[G/T]AAATTTGACTCTCCT | 51429 |
| rs142409992 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157875446 | ATGAACACAGACCCC[A/G]GAAACTGCAAATACC | 51429 |
| rs142418471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157795681 | GTGAAATATTAACAA[C/T]TGTAAAATTAAAGTG | 51429 |
| rs142444843 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157797525 | AATAATAGATAGATC[A/G]ATTGTCTAACTCTTC | 51429 |
| rs142455056 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SNX9 | GRCh38.p7 | 6:157762686 | TCCCGGAGCCCGCTG[C/T]GGCTAGGGAGGATGC | 51429 |
| rs142469263 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157764058 | TCATGCAAATGTATA[C/G]TTGCTTTGTGTATGC | 51429 |
| rs142474654 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157763580 | AGAGAGACCAGGGAG[C/T]GTCCCTTCCAGGTGG | 51429 |
| rs142574715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157815480 | AACTCCCAAAGTGTC[A/G]GGATAATGGGCATGA | 51429 |
| rs142576239 | in-del | -/AC/ACAC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157927930 | AAGTATAGACAAGTA[-/AC/ACAC]AACACACACACACAC | 51429 |
| rs142623267 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | SNX9 | GRCh38.p7 | 6:157907474 | ATTTTATAGTAGAGA[C/T]GGGGTTTCACCATAT | 51429 |
| rs142626617 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157834585 | GTCTCAAACTCCTAG[A/G]CTCAAACGATCCTCC | 51429 |
| rs142644544 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SNX9 | GRCh38.p7 | 6:157836265 | GAAACATCTTGTGCA[C/T]GTTCTGGAGTTTTCA | 51429 |
| rs142646982 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157862500 | TGAAGATTTACATAT[G/T]TTATTTTTTAATTGT | 51429 |
| rs142664591 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157939122 | TGGGTGTGTCATTTT[A/G]GGCACAATTTTTTTG | 51429 |
| rs142680884 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157764744 | GGAATGTGGCTGCAG[G/T]GATGTGGCCTGACAC | 51429 |
| rs142692672 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157731229 | AAAACTCCTGACCTC[A/G]TGATCCACGTGCCTC | 51429 |
| rs142712356 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157754296 | CTATAAACTAAGTTT[A/C]TCCCAAAGTTAGTTC | 51429 |
| rs142734039 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157941893 | CAGGACGTGGGCCCT[A/G]TGCTCTTTAAATGCA | 51429 |
| rs142759181 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157825409 | AACTAGTGCAGGTAT[A/G]TATAGTGAAATTTTT | 51429 |
| rs142798257 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157775864 | GAGAAAGGTGGAGAG[C/T]CATGTTTGAGGAGTG | 51429 |
| rs142819909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157808299 | TAGCTCCTATAGAAA[C/T]AAAAATATATATTTT | 51429 |
| rs142823367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157883239 | TATTTTTTATACATA[A/G]TGCTCTCGCACACTT | 51429 |
| rs142842787 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157880670 | AGTTATTGAGAGGCG[G/T]GCTCTGCATCCTTGA | 51429 |
| rs142846698 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157855512 | TTTCCCTAAACCTTA[C/T]GCCCTTACCAGCATG | 51429 |
| rs142850582 | snp | A/T | 0.000214184 | 0.0103463 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157910024 | AGACAAACAAGTCAC[A/T]GGTGAGTGTGTGTAA | 51429 |
| rs142854640 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157866840 | TATGTCTCTGTCTTC[A/T]GTTTCTGAGAGTCAG | 51429 |
| rs142860612 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157747381 | CATCTCTTGCAGGAA[G/T]AGTTCACATTTTTTA | 51429 |
| rs142912789 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SNX9 | GRCh38.p7 | 6:157853285 | ACATTTGGCTTGTAC[A/G]TGTTGTTCTTGAGAA | 51429 |
| rs142913709 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157928535 | TGGTTATATTTGGCC[C/T]GAGTATCCCCACAGC | 51429 |
| rs142941389 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SNX9 | GRCh38.p7 | 6:157745455 | TTATTCTCTTCTCTC[A/G]AATCCAAACCTAATA | 51429 |
| rs142969211 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157725420 | CTCCACTTCAGGGAC[C/T]TTAATTATGGATTAA | 51429 |
| rs142982499 | snp | C/T | 0.134119 | 0.221521 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889228 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 51429 |
| rs143017646 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889613 | CTTTACAGTAAAAAT[A/T]TTTCTGTCTTCTTCC | 51429 |
| rs143051512 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157845458 | TATTTTGACAGTAAA[C/T]TTTTTAGCCATCTAC | 51429 |
| rs143056607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157800751 | ACTGCATACTGTGGT[A/G]ACTCATTCCTTACTT | 51429 |
| rs143058557 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157738857 | ATGGGGAAAGGATTC[C/T]CTATTTAATAAATGG | 51429 |
| rs143080780 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894362 | TGATCCTCCCGCCTC[A/G]GCCTCCGAAAGTGGT | 51429 |
| rs143125845 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157802679 | TAAGTTATCTGCAAC[C/T]AAAGTAGTTTGACTA | 51429 |
| rs143130973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157727754 | CCTGGGTTTAATTAT[C/T]AGCTTAATGTTGAGG | 51429 |
| rs143132885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157880489 | ACAGTTCTATCAGCA[C/T]GTCTCCTTTGTATCT | 51429 |
| rs143134060 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SNX9 | GRCh38.p7 | 6:157851162 | GCTCAGAAGGCTGAG[A/G]CAGGAGAATTGCCTG | 51429 |
| rs143134605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157926432 | TCTTATATTTTAGAA[A/G]AGCATTTACCTTTTT | 51429 |
| rs143151603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157774794 | TCCACCCTCCCCGAT[A/G]GCCTGGGGAGAGGGA | 51429 |
| rs143191766 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157735253 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAGGACC | 51429 |
| rs143208529 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157930148 | CAATAACTACCTCTG[-/C]CTCTTCCTCTACTAG | 51429 |
| rs143230208 | snp | A/G | 0.145305 | 0.227022 | utr-variant-5-prime, intron-variant | SNX9 | GRCh38.p7 | 6:157823330 | CCGCGCCGGGGCCCA[A/G]CCGGAGCCGCCGCCC | 51429 |
| rs143232627 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157899211 | ATTACTTCTTCACTC[A/T]CATCTTTTTCTCCCA | 51429 |
| rs143247316 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157864796 | GTATTTTGGGAGGCC[G/T]AGGCGGGCAGATCAT | 51429 |
| rs143247399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157819541 | CTCATCCTCCGATCC[C/T]TACATTAGGTGACCA | 51429 |
| rs143255297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157941505 | AAATTTTTCTTACCT[C/T]TGCTTAGTAATTTTG | 51429 |
| rs143300731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157787322 | GTTACGCCATCAGCT[C/T]TCCTGGGTCTCCAGC | 51429 |
| rs143300961 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157728879 | CCAAGGTGGGTGGAT[C/T]ACTTGAAGTCAGGAG | 51429 |
| rs143310843 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157756035 | AGATGTTTGCCAGTA[A/T]TCACATCTGATGACA | 51429 |
| rs143312841 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SNX9 | GRCh38.p7 | 6:157823783 | GACGGAAACTTCCCG[C/T]AGCCCGGGGAGGCCC | 51429 |
| rs143323054 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | SNX9 | GRCh38.p7 | 6:157722011 | TAAGTCCTCCTTTGG[G/T]TCCAGGGGCTGAATC | 51429 |
| rs143361302 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157862938 | CTCATGAGGAGATAC[A/G]TTGGCTCCAGTAACA | 51429 |
| rs143369219 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157939394 | GAAAGCTCTAGACTT[G/T]ATGCAGGCATTAAGA | 51429 |
| rs143373781 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157765915 | GGTCCATGAGCATTG[C/T]TGTCTGGGAGCACGT | 51429 |
| rs143377958 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SNX9 | GRCh38.p7 | 6:157837780 | TCAGTAAGAAGTAAC[A/G]GGTGTCTAAATAAGA | 51429 |
| rs143405791 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157732669 | AGAACTTATTCATCC[C/T]GTTTAACTGAACTTT | 51429 |
| rs143406891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157941315 | ATGAGGTCACCCAGC[C/T]GTCCCTGGGACTCCG | 51429 |
| rs143431008 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157866725 | TTAATGTGGCTAAAG[A/G]TGCTGCATTATCATT | 51429 |
| rs143439048 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157924582 | AGTTAGCTCAGTGAA[A/G]GTTAAAGTTTTCCCA | 51429 |
| rs143446105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157882356 | TGGTCACCTAAGAGC[A/G]CTGATGGAGATGTAC | 51429 |
| rs143471637 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157805352 | GGACTCTTACCTGAA[C/T]CTCCTGGTTGCTCTT | 51429 |
| rs143472724 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157770041 | ACAAGAGGTCATGCA[G/T]TCTCATTTTGCACCA | 51429 |
| rs143472781 | snp | C/T | 0.0016797 | 0.0289315 | missense | SNX9 | GRCh38.p7 | 6:157938739 | GCATCATGTCTTACG[C/T]GTTGCAAGGTAAGAT | 51429 |
| rs143482471 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157868912 | CTTGGTCCACGCCTC[C/T]GCCTCTGGGCCCCAC | 51429 |
| rs143491798 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SNX9 | GRCh38.p7 | 6:157724262 | CCTCTCTGAACAGCC[A/G]CCCAGCACTTCAGTG | 51429 |
| rs143491839 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157762996 | CTCTCCTGCATCTGC[A/T]TTTTAATGGCCTTCA | 51429 |
| rs143507384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157830785 | TAGAAAATTCTCAGC[A/G]GTTATTCATGAAAAT | 51429 |
| rs143517131 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157944806 | AAGGGATGGGGGAAA[C/T]GGAGATGGCACGGGC | 51429 |
| rs143542981 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157855120 | TACACAAGCAAATGC[A/T]TGTACTGCATCGCTG | 51429 |
| rs143549601 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157861435 | GAAACTGTAGAAAGC[A/G]TGCTCATCAGGCTTT | 51429 |
| rs143550048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157930009 | TCTTTGGCTACATTT[A/G]TGTCATAATGGTAGA | 51429 |
| rs143575123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157813785 | ATCAGAGAACAAAAC[A/G]CGCACTGGTCCTTTC | 51429 |
| rs143575217 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157747167 | CAGGTCTGTGGCCCC[A/G]AGACTGAGGACCCCT | 51429 |
| rs143643278 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157784841 | TCCTACGCTGTTTCT[C/G]TGGCAAATTAAACAC | 51429 |
| rs143652434 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157859931 | GGGTCATGTTATAGG[A/C]GTCAGCAAATTTTGG | 51429 |
| rs143666331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157798878 | ATAAAATGGTTGCTC[A/G]GGAAATACATTCAGA | 51429 |
| rs143666502 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157846682 | AAGCTGAGAGCTGGG[A/G]AATAAGTATTCAGTG | 51429 |
| rs143668501 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157921417 | GTTTACCTTTTGCTA[A/C]ATAGCTTTCTACCCA | 51429 |
| rs143711728 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157739299 | AAATGATATGAACAG[A/G]CACTTCTCAAAAGAA | 51429 |
| rs143722672 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SNX9 | GRCh38.p7 | 6:157758387 | GGAGAATATTATACA[A/G]GGAAATGGCAATATC | 51429 |
| rs143728592 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157801803 | GTGTCTGATGAGAAC[A/G]CGTGCTCTGACAGAA | 51429 |
| rs143788800 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SNX9 | GRCh38.p7 | 6:157920121 | GTAACTGTAACTCGA[C/T]GTAACTCATTCAAAG | 51429 |
| rs143796571 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | SNX9 | GRCh38.p7 | 6:157796275 | ACTATTAGTAAGGAG[A/T]ATAGCTTTTTTAAAT | 51429 |
| rs143802999 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157923278 | TACATAGAAACTATG[A/G]TTCTGTGGTAAGTAG | 51429 |
| rs143833953 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157902538 | AGAGACGCATCGAGT[G/T]TTCCAGTCAGGAAGC | 51429 |
| rs143839572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157848800 | TAGGGGAAGGGTAGT[A/G]TTATAAGGCCGTCCA | 51429 |
| rs143864453 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157734148 | TACATAAATGAAGAC[A/G]GAAAACAAATACATA | 51429 |
| rs143889952 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157740063 | TGTAACAAACCTGCA[C/T]ATTCTGTACATGTAT | 51429 |
| rs143904486 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | SNX9 | GRCh38.p7 | 6:157744476 | ATGCAGATGAGTGGA[A/G]ACAGCCATGAGCAGA | 51429 |
| rs143914377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157809666 | TTAAAATGGGCAAAG[A/G]ATTTGAACAGATACT | 51429 |
| rs143931603 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157730214 | CTGTTTTTTTTTTTT[A/T]AAAAAAAAAAAAAAA | 51429 |
| rs143970755 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157899926 | GTATATGTGCAAGTG[C/T]GTGCCTGTGGGTGTG | 51429 |
| rs143971045 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157944448 | TGTATAAATGTTTTA[C/T]ACGAATGTAAGAGCA | 51429 |
| rs144020843 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SNX9 | GRCh38.p7 | 6:157829270 | TTGTCTTTAACCTAC[A/G]AGTTGTCAGAATTGT | 51429 |
| rs144031148 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157781329 | GGGTGATGTGACCAC[C/T]TGCTCTGTTAGGACA | 51429 |
| rs144039132 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157903070 | GAGAGACCTAAATAA[A/G]GCTGTAGTCTATGCC | 51429 |
| rs144044634 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SNX9 | GRCh38.p7 | 6:157879252 | AACCGGAATGTAAAT[A/G]TCTGTCAGCAGGGGA | 51429 |
| rs144064354 | in-del | -/G/T | 0.00557542 | 0.0525036 | downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157945375 | TTTCTTACAAAAGTA[-/G/T]CCTGCTGGGTCTGGG | 51429 |
| rs144082310 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157784973 | AAGCAAAGGCCAGAC[A/G]TGGTGGCTCACATCT | 51429 |
| rs144088786 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157901047 | TTTCCATTCCCAGAG[C/T]TATGAATATCTGCTT | 51429 |
| rs144090871 | in-del | -/AAAC | 0.325799 | 0.238232 | intron-variant | SNX9 | GRCh38.p7 | 6:157937623 | TTATTATTAAAAAAG[-/AAAC]AATCTATAATTCCCA | 51429 |
| rs144094722 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157788368 | TACAGGATCATAAAT[C/G]ATTGAGCTAAGGCAT | 51429 |
| rs144095877 | in-del | -/TCA | 0.0248432 | 0.108648 | intron-variant | SNX9 | GRCh38.p7 | 6:157753504 | TCGGGCTGTTTCCTT[-/TCA]TCATCACAAGGTGGT | 51429 |
| rs144103001 | in-del | -/C | 0.0252325 | 0.109451 | intron-variant | SNX9 | GRCh38.p7 | 6:157770644 | AAAATAATAATAATA[-/C]AAAAAATTAGCCAGA | 51429 |
| rs144110946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157767728 | GAAGATCCTGTTTTC[C/T]CTTTAATCACAAATC | 51429 |
| rs144112749 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157839872 | ACCTTGCTGGTTGTG[C/T]GCAGTATTGGGGCGT | 51429 |
| rs144121689 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SNX9 | GRCh38.p7 | 6:157904667 | GTGAGCCGAGATCGC[A/G]CCACTGTACTCCAGC | 51429 |
| rs144125441 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157786238 | TTGTTTGATAGAGAC[C/T]GGGTTTTGCTATGTT | 51429 |
| rs144141288 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | SNX9 | GRCh38.p7 | 6:157730397 | GGGTGTGGTGGTATG[C/T]GCCTGTAGTCCCAGC | 51429 |
| rs144157947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157790268 | CTGCAGTCTCTAACA[C/T]AGCCTGACTTTCCAA | 51429 |
| rs144160824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157866119 | ATTTTAAACACATAC[C/T]TTGTTTTTACCACGG | 51429 |
| rs144184635 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157934108 | TACTATGCGATCTTG[A/C]AATAATGTAAATGGG | 51429 |
| rs144189614 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SNX9 | GRCh38.p7 | 6:157942389 | CACACTCAGCAGTGA[C/T]AGCAGGGTGTGGCCA | 51429 |
| rs144201668 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157927293 | TTCAGCCAGTGTAGC[C/T]GCAGCCGAAACTCAA | 51429 |
| rs144201780 | in-del | -/AACAAC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157821033 | TCTTGCTCTTTTTAA[-/AACAAC]AACAACAACAAAAAA | 51429 |
| rs144205788 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SNX9 | GRCh38.p7 | 6:157937914 | AAATATCATGAAGGG[A/G]TACCATAGGTAAATT | 51429 |
| rs144205871 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157891144 | TCAAGCGATTCTCCT[C/G]CTTCAGCCTCCCAAG | 51429 |
| rs144221590 | snp | A/C | 0.02016 | 0.0983543 | intron-variant | SNX9 | GRCh38.p7 | 6:157739749 | GTGGCACATATACAC[A/C]ATGGAATACCATGCA | 51429 |
| rs144234185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157809503 | TGGACTTATTTTGGT[C/T]TTCGAAAGATACCAT | 51429 |
| rs144242213 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157883411 | TTCAGAGTCTCCTCT[A/G]TTGCCTTCTGGAATA | 51429 |
| rs144257473 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SNX9 | GRCh38.p7 | 6:157721804 | TGCAAGCGACCAGGG[A/G]TGTGTCTGTTGTTGT | 51429 |
| rs144262025 | snp | A/T | 0.000296946 | 0.0121813 | missense | SNX9 | GRCh38.p7 | 6:157942833 | AGCCGCTTTCCAGTG[A/T]TGTAGGACAGAACGG | 51429 |
| rs144265051 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157773678 | ATGATCAATCCCCAA[C/G]ATCAGGGAGGAGGCA | 51429 |
| rs144271439 | snp | C/T | 0.000439917 | 0.0148245 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157896970 | CTGGGACACTGCCTT[C/T]GGCCACCCCCAGGCC | 51429 |
| rs144309479 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157719621 | TTAGAAGAGAACTCA[A/G]CGAAGATAGTGCTGT | 51429 |
| rs144312368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157932490 | TTTTCTTGCTAGCTC[A/G]TTTGCCTTTTTTTGC | 51429 |
| rs144328578 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SNX9 | GRCh38.p7 | 6:157829276 | TTAACCTACAAGTTG[C/T]CAGAATTGTCTTTAA | 51429 |
| rs144330117 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157778240 | CCATCATCACTGTGA[A/T]TCTATTCGTGCCCAA | 51429 |
| rs144336601 | snp | C/G | 0.00795939 | 0.0626292 | intron-variant | SNX9 | GRCh38.p7 | 6:157858341 | AGCCTCCACCACCCG[C/G]GTTCAAGTGATTCTC | 51429 |
| rs144343625 | snp | C/G | 0.0596104 | 0.162024 | intron-variant | SNX9 | GRCh38.p7 | 6:157815327 | AAGCAATCCTCCCAC[C/G]TCCCACCTCAGCCTC | 51429 |
| rs144360101 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | SNX9 | GRCh38.p7 | 6:157749644 | CTGCCTCCACCTCCC[A/G]AGTAGCTGGGACTAC | 51429 |
| rs144363121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157725891 | CGTTTGAGTTACCTG[A/G]TTCTTCCCGAACACC | 51429 |
| rs144387514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157881992 | CAGAGCAGATGAAAC[A/G]GCCTTCTATTATTGG | 51429 |
| rs144420357 | in-del | -/GGGGCA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157939957 | ACTCCTCTAGAGTTG[-/GGGGCA]GGGGCAGGGGCAGGG | 51429 |
| rs144429389 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157764316 | TTGGTAAAACTGAGG[A/G]GGAAATATAAATTGA | 51429 |
| rs144438851 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157862155 | ACTGAAACCGAGGAA[C/T]GTGAAACTGTGGAGG | 51429 |
| rs144447636 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157768160 | ATCCACGCTAACCCC[A/C]GCCTAACCTACTCCA | 51429 |
| rs144448616 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157884613 | CCCCCCCGTATGAAT[C/T]CTTTTTAGTTGGTAA | 51429 |
| rs144462671 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157771379 | AAGCCATAGAGTTTT[A/G]GGTTCAAACATCAGC | 51429 |
| rs144462942 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157844095 | GGCCTGGCTGGTCTC[A/G]AACTCCTGGCCCCAA | 51429 |
| rs144528174 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | SNX9 | GRCh38.p7 | 6:157737638 | TTTGAAGAGTTTTTC[A/G]TGTCTCTATCTCCTT | 51429 |
| rs144528446 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157772818 | AGCCTCAATATGGGA[A/G]ATCTTTGGGTGGAAA | 51429 |
| rs144530870 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157848647 | TGAACTCTGTAAGCA[C/T]CTCTTAGGTGGCAGA | 51429 |
| rs144542819 | in-del | -/ATG | 0.347253 | 0.230308 | intron-variant | SNX9 | GRCh38.p7 | 6:157897191 | GAGTGTCCTACAGTC[-/ATG]CATGACACTGTCTAC | 51429 |
| rs144557871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157918327 | TTAATATCTTCCTGA[C/T]GTAGTGACCTCTTAT | 51429 |
| rs144587703 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157798225 | CCTGTGAGGGCGCAA[A/T]GAGACGAACTCACCA | 51429 |
| rs144601304 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | SNX9 | GRCh38.p7 | 6:157915803 | GCACTCCAGTCTGGG[C/T]GACAGAGTTAGACTC | 51429 |
| rs144603280 | snp | A/G | 4.94271e-05 | 0.00497102 | missense | SNX9 | GRCh38.p7 | 6:157909918 | TGTAGAACACTAATC[A/G]ATCTGTAAACCACAG | 51429 |
| rs144603745 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | SNX9 | GRCh38.p7 | 6:157917740 | AATACAATGTAAATG[C/T]TATGTAAATCATTGT | 51429 |
| rs144609838 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157875639 | TGCCTGTGAAAGTCT[A/G]CCAGATCCAGGCACT | 51429 |
| rs144610307 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157920491 | CACCATGTCGAACAC[A/G]TGGGGTGGGTGGCAC | 51429 |
| rs144624939 | snp | A/G | 0.000478323 | 0.0154574 | missense | SNX9 | GRCh38.p7 | 6:157896831 | CCTCTCAATAGGTTG[A/G]CAGTGGCAATGACCC | 51429 |
| rs144628907 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SNX9 | GRCh38.p7 | 6:157797607 | GGTTTCTAAATATCA[C/T]TCTTTACTAAAAGGA | 51429 |
| rs144641619 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157876321 | GCTAGGTGTGGTGGC[A/G]GGCACCTGTAATCCA | 51429 |
| rs144647472 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | SNX9 | GRCh38.p7 | 6:157878460 | TTTGAGACGGAGTCT[C/T]GCTCAGTCGCTCAGG | 51429 |
| rs144662956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157919047 | TAATCCTTATATTTC[C/T]GGTGCTGCTTATTTG | 51429 |
| rs144672623 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157799166 | AAAACTCACTCACTA[G/T]CATGAGAACAGCCTG | 51429 |
| rs144676279 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SNX9 | GRCh38.p7 | 6:157877109 | GACCAGCTATTATCT[C/T]AAGATAGGTGGAGGC | 51429 |
| rs144678561 | in-del | -/GGGGGG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157807256 | TTGAAAAATGTGGCT[-/GGGGGG]GTTGCAATTGCATTC | 51429 |
| rs144684306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157848045 | AAGCCCTTACTCTGT[C/T]GCATCACCTGATTAA | 51429 |
| rs144687072 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157921766 | TGGTTAGTTATTTCT[C/G]ACTTCCTCCAGTGAC | 51429 |
| rs144693196 | snp | C/T | 0.000230631 | 0.010736 | missense | SNX9 | GRCh38.p7 | 6:157909920 | TAGAACACTAATCGA[C/T]CTGTAAACCACAGGT | 51429 |
| rs144705345 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | SNX9 | GRCh38.p7 | 6:157752949 | CTTTTAACAAGCATG[A/C]TGCCTTGAAGCATTT | 51429 |
| rs144742027 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157765141 | GTTAGAAAGAGACTC[C/T]TCTTGCTTAGACAAT | 51429 |
| rs144751276 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157817586 | GCACTTGAGCCAGGC[A/G]TGGTGGCTCACGCCT | 51429 |
| rs144778454 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | SNX9 | GRCh38.p7 | 6:157789390 | CAGGAGCCATATGGT[A/C]TCTGTTAAAACACCC | 51429 |
| rs144790289 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157852894 | TTTTTGTCATACATT[C/T]TATTTCCCAGTATTA | 51429 |
| rs144791455 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SNX9 | GRCh38.p7 | 6:157777241 | AAAAATTAGCCAGGC[A/G]CAGTGGCGGGTGCCT | 51429 |
| rs144810489 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, downstream-variant-500B | SNX9, LOC107986663 | GRCh38.p7 | 6:157715141 | AGGCTGAAAGAATTG[C/T]GGCCGTGAATAAACA | 51429 |
| rs144830917 | snp | C/T | 0.0107246 | 0.0724382 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822183 | TTTTAAACCCCATTA[C/T]TGAATATAACTAGTG | 51429 |
| rs144872884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157720537 | TGGGACCCAGCTGGG[C/T]TCATGAGACACAAGC | 51429 |
| rs144904114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885124 | GTAAATTTTTAGTGT[C/T]TTAATTATCTTTATT | 51429 |
| rs144914341 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157723885 | GAGACCAAATATGTG[A/G]ATTTTTTCCTTCAAA | 51429 |
| rs144963813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157845065 | AGGCAATTTCAGGAT[C/T]ACAGGCTTCAGCCAC | 51429 |
| rs144983243 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157934952 | TACCAATTGGAAGAG[C/T]CTACCACTGGCCAAA | 51429 |
| rs144987892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157855806 | CAGTGGCACAGTCTC[A/G]GCTCACTGCAACCTC | 51429 |
| rs144998301 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157763293 | TGAGGAAGCTGCTCC[A/G]GGCTTCCAGGCCAGA | 51429 |
| rs145004461 | snp | A/C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157728467 | TCGACCTTTGCCTTC[A/C/G]CATCTCCCCTTGGGA | 51429 |
| rs145008407 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157817402 | AGGACTCACAAGGGA[G/T]GGAGGCTGTAATTTG | 51429 |
| rs145014610 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SNX9 | GRCh38.p7 | 6:157898119 | CCGGGAACTAGGGAC[A/G]CAGACCAGATGGCTA | 51429 |
| rs145059338 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157778876 | TGTTGAGTATGAGTA[A/C/T]GAGTATGTTGTAGAG | 51429 |
| rs145072622 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157891348 | ATCATTTTTTCTGTA[A/G]TCACATGCTGAAAAT | 51429 |
| rs145090700 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157858437 | ATGTTGGTCAGGCTG[G/T]TCTCAAACTCCTGTA | 51429 |
| rs145091944 | in-del | -/GCTAAGATAAC | 0.0352966 | 0.128072 | intron-variant | SNX9 | GRCh38.p7 | 6:157735910 | GGGAGGTTGCAGTGA[-/GCTAAGATAAC]GCCACTGCACTCTAA | 51429 |
| rs145103756 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157844595 | AATCCTTGTTTTTTT[G/T]TTTTGTTTTTTTTTT | 51429 |
| rs145130153 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157799897 | TCAAACCATATCACT[A/G]CTATAATGTGGACAG | 51429 |
| rs145143619 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157774268 | GAGTGGAGGAGGTGG[A/G]GTAGTGGAGGAGGGA | 51429 |
| rs145152161 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | SNX9 | GRCh38.p7 | 6:157749880 | ATTAGGGGAAAAAAA[A/T]TCCACTTACTATAAC | 51429 |
| rs145159310 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157941199 | GAAGCAGGGGTCTTG[A/G]ATGCTAGTTGCAAGG | 51429 |
| rs145192815 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | SNX9 | GRCh38.p7 | 6:157765597 | CCTGACCTCGTGATC[C/T]GCCCGCCTCGGCCTC | 51429 |
| rs145202393 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157736976 | TTGCATATGTTGAAC[C/T]AGCCTTGCATCCCAG | 51429 |
| rs145275440 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157870431 | ACACACGCACACTCA[C/T]ATGCTGTCACACAGA | 51429 |
| rs145310863 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157841900 | TAAACATGGACAAAA[A/G]TAGAACAGCACAGTG | 51429 |
| rs145385573 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157837116 | TATTTTATCTAACTG[G/T]GTTCATATGATGCAG | 51429 |
| rs145397897 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157791683 | CAGTCCAGAGCAATT[A/G]GTAATTAGCCCACAT | 51429 |
| rs145416462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157914569 | ACAACCTTGACCTCC[C/T]GGGCTCAAGCAGTCT | 51429 |
| rs145422162 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157799575 | CTGCTGATAAAGACA[C/T]ACCCGAGACTGGGAA | 51429 |
| rs145430665 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157877650 | GTGAGCTGCTTGGGA[C/G]GCTCTGATTGCCTGT | 51429 |
| rs145433369 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157780426 | TGTGCCTCCATCCTC[C/G]TAGGGACAGAATTCT | 51429 |
| rs145453999 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157735412 | AAGCCCAGACCTGGC[C/T]GGGCGTGGTGGCTCA | 51429 |
| rs145459629 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157730211 | TAACTGTTTTTTTTT[A/T]TTTAAAAAAAAAAAA | 51429 |
| rs145465376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157754166 | CCTCCAGCTGCACGA[C/T]TCCTAAATCATAATT | 51429 |
| rs145473689 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SNX9 | GRCh38.p7 | 6:157849133 | AAAGAAAATAGTTCA[A/G]TAAGTCTGGAATTTA | 51429 |
| rs145474630 | in-del | -/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157834149 | TGTGGTGTCCACTGT[-/G]GTTTTTTTTTTTTTT | 51429 |
| rs145475063 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157795560 | TTATATAAGAAAATA[C/T]CCTTAGGTTTTTGAG | 51429 |
| rs145492684 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157724776 | TTGGAACATTGACTT[C/T]CATTCTTTGGAATCT | 51429 |
| rs145495016 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157741076 | TCTTGGCCGGGTGCC[A/G]TGGCTCATGCCTGTA | 51429 |
| rs145502982 | snp | A/G | 0.0980852 | 0.198549 | intron-variant | SNX9 | GRCh38.p7 | 6:157783731 | CTCACTGCAACCTCT[A/G]CCTCCCAGGTTCAAG | 51429 |
| rs145543128 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157898339 | TAAAAGCAGAATGGG[C/T]GGTGGAGGCTGCAGA | 51429 |
| rs145559072 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157791039 | TCGTTGGAGTCACTC[C/T]GATGCATTTTAGGGC | 51429 |
| rs145571052 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157757697 | TACAGTGACCTCAGA[A/T]GTGCACAGGGCACCC | 51429 |
| rs145575588 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157854550 | TGTACATGCAAACAC[A/G]TATGGCAAATTTATA | 51429 |
| rs145589455 | snp | A/G | 0.000307953 | 0.0124049 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157867633 | CACAATCACAAATCC[A/G]GTAAGAGAACTGTAC | 51429 |
| rs145635560 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157935901 | AAATCAATAATAAAA[G/T]TTTAACAAGTGAAAA | 51429 |
| rs145640866 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157818309 | GGCCAGTCTATTCTT[C/T]TCACGTTTTTCTGCC | 51429 |
| rs145641917 | snp | C/T | 0.0253631 | 0.109719 | intron-variant | SNX9 | GRCh38.p7 | 6:157940863 | GGGAAAACTGATTGA[C/T]GTTCTGATTTGGGTT | 51429 |
| rs145642572 | snp | A/G | 0.0554779 | 0.157039 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894161 | GTCGCCCAGTCTGGA[A/G]TGCAGTGGCGTGATC | 51429 |
| rs145673849 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822625 | GGGGCTTCAAGCCAG[A/G]ACCCCGGCCTGAGGG | 51429 |
| rs145674976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157898379 | GCCCCTGCTGTCGCC[C/T]GTGGATCACTGCATT | 51429 |
| rs145699304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157735822 | AAATACAAAATTGGC[C/T]GGGTATGGTGGCACA | 51429 |
| rs145708491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157795850 | TGTTGGAACAGCGTC[C/T]GGGGTGGTATAACAC | 51429 |
| rs145717392 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157721164 | CACACCCCTGCAATT[A/C]CAGCTACTCCAGAGG | 51429 |
| rs145750940 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885443 | CCGTATTTTGAGCTA[A/C]AGTGGTTAGATTTTT | 51429 |
| rs145750997 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157770287 | GTCCATCAGAGCAGT[G/T]CACGCATGGAAGACT | 51429 |
| rs145766882 | in-del | -/TTTG | 0.144632 | 0.226711 | intron-variant | SNX9 | GRCh38.p7 | 6:157852586 | GTGCTACTTTTTTGT[-/TTTG]TTTTTTTGAGACAGG | 51429 |
| rs145795488 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157908751 | GCTCAAAACTTACAC[A/G]AGGTCTCTACACCCC | 51429 |
| rs145842390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157769742 | TGTGGAGGATTTTTG[A/G]TGGAGGCCCATGTGG | 51429 |
| rs145846562 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | SNX9 | GRCh38.p7 | 6:157841353 | AGATAGAAATACAGA[C/T]TTTATTACCTACAGG | 51429 |
| rs145852132 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157744988 | GACCTTGTGATCCAC[C/G]CACCTCGGCCTCGCA | 51429 |
| rs145861911 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | SNX9, LOC107986663 | GRCh38.p7 | 6:157714184 | CAATCTGGCAAAGGT[A/G]CCAGAAGACAGAGGT | 51429 |
| rs145886016 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157915888 | GTAAATGGTACTGTT[G/T]TTTAAATTTCCATTT | 51429 |
| rs145951820 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | SNX9 | GRCh38.p7 | 6:157762782 | CTCTAGGGGGCAGCA[A/T]CTTGGGGAGAAGCAA | 51429 |
| rs145955851 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157764147 | TTATTCTGGAGCTAA[A/C]ATAGTCTTCCGTGGT | 51429 |
| rs146006225 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157908194 | CTCTCTTCCTTCAGC[A/G]CAATCTGTGTGATTT | 51429 |
| rs146021427 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157790628 | GTGGACTCGGTCCTT[C/G]GGAGGATTCAACTGG | 51429 |
| rs146036872 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157809942 | CTTATCATATGATCA[C/T]TCAATTTCATTTCTA | 51429 |
| rs146040620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157913628 | ATACAGAACAGCTCC[A/G]TCACCTCCCCAGGTT | 51429 |
| rs146041071 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157866169 | ATGCACAGCAGTGTT[C/G]CAAGGAGTCAGTGTT | 51429 |
| rs146056236 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157852142 | GGAATTTGCTGGATC[A/G]TATGGTAATTCCGTG | 51429 |
| rs146073614 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157744354 | AGGCTCTTCTTGCCT[A/C]TTAAGTACATCATGC | 51429 |
| rs146077596 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157747479 | GCAGTCAAGTTTTCT[C/G]TTCCATCTTCATTCA | 51429 |
| rs146080464 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157815053 | AAATTGTTTTGCTTT[C/T]CTCTGCTTTTTCTCC | 51429 |
| rs146086200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157807442 | GCATACTTAGCTAAT[A/G]CAGACCCTACTCTCT | 51429 |
| rs146101013 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157929617 | TTCAGTTAAAAAAAA[A/T]GTTTTATATTTTGAA | 51429 |
| rs146126994 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889831 | AGAAATGCTAGTCTT[C/T]ATTCTTTTCTTTATA | 51429 |
| rs146142388 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SNX9 | GRCh38.p7 | 6:157772996 | AGCTTCTCCCAACGG[C/T]TCTTGGTATTACAAA | 51429 |
| rs146181775 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157907445 | CACCACCACGCCTAG[A/C]TAATTTTTTTTGTAT | 51429 |
| rs146194530 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157730938 | GCCACTGTGCCCGGC[C/G]TTACCTACATTTTCA | 51429 |
| rs146216806 | in-del | -/TC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157787419 | AACTCAATCTCTCTT[-/TC]TCTCTCTCTCTCTCT | 51429 |
| rs146235098 | in-del | -/CT | 0.0260105 | 0.111035 | intron-variant | SNX9 | GRCh38.p7 | 6:157902493 | TGGTACATAAAACCC[-/CT]GTTTTACTGCAGGCA | 51429 |
| rs146281355 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157831239 | TTTTTCCTTGAGTTG[C/G]TTGTTTTCCTTGGAA | 51429 |
| rs146282332 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | SNX9 | GRCh38.p7 | 6:157904602 | TGTAGTCCCAGCTAC[C/T]TGGGAGACTGAGGCA | 51429 |
| rs146300029 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157815286 | GGCCTGATCTTGGCT[C/T]ACTGCAGCCTCGGAT | 51429 |
| rs146300484 | in-del | -/AA | 0.282369 | 0.247896 | intron-variant | SNX9 | GRCh38.p7 | 6:157753233 | TTTCTTTTTAGTGGC[-/AA]AAAAAAAAAAAAAAA | 51429 |
| rs146301382 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889028 | GTGTAAGGAAAGAAA[C/T]GAAGAGGCATCTCAG | 51429 |
| rs146303914 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157772773 | TGAGGTTAAGAAAAC[C/G/T]AGGTTAAGGCACATT | 51429 |
| rs146320136 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157716239 | GGTAAGAAGAAGGTG[A/G]CTAAGGCTGCCTCCA | 51429 |
| rs146323816 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157775339 | CTCCAGCCTGGGTGA[C/T]AGAGGAGACTCTGTC | 51429 |
| rs146333045 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157755482 | ACAACAAAGACTACT[G/T]ATAGACTGTTGGGCA | 51429 |
| rs146333273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157866988 | CAGGGTCTCACTGTC[A/G]TGCAGGCTGGAGTGC | 51429 |
| rs146353791 | in-del | -/GGGTGGGGGCCACAAGATCAGATGCCCAGTTTATTGATCG | 0.0629771 | 0.165899 | intron-variant | SNX9 | GRCh38.p7 | 6:157844401 | ACTGAGTCAGTTCCT[lengthTooLong]GGGTGGTGCCAGCTG | 51429 |
| rs146371697 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157928354 | TTATTTTATTTACTT[A/T]AGAATAATTTTAAAA | 51429 |
| rs146384790 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157809836 | TGTGGAGCAACTAGA[A/T]ATCTCACATGTTTCT | 51429 |
| rs146404132 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SNX9 | GRCh38.p7 | 6:157884384 | AGTTCTCAAAAGTCT[A/G]TTTTTAGGCCATTTT | 51429 |
| rs146404365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157931838 | CTCAGCATGAGGATG[A/G]TGTCTCTGCATCTGG | 51429 |
| rs146452907 | in-del | -/GGG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157817441 | GCTCTAAATCATGGC[-/GGG]GGTCACAGCAAATGT | 51429 |
| rs146456808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157758628 | TAAACAATGGTAAGT[A/G]GGAGAGGTCAGGGGT | 51429 |
| rs146469047 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157763592 | GAGTGTCCCTTCCAG[A/G]TGGAACCCCTCCTCC | 51429 |
| rs146470654 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157920203 | GTGTCTCCTTTACTT[C/G]TATGTACAGCCTCAG | 51429 |
| rs146471322 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157859197 | ATGAAAAGAAATATA[A/C]TGAGAAACGTCACTT | 51429 |
| rs146483363 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | SNX9 | GRCh38.p7 | 6:157783760 | AGCAATTCTCCTGCC[A/G]CAGCCTCCTGAGTAG | 51429 |
| rs146488776 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157786393 | ATCTACTTCTTGGAG[C/T]ATCTGACTAACCCAA | 51429 |
| rs146489977 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157862541 | TTTAAAGATGAGGAG[A/C]AACACTGTTGAAGAT | 51429 |
| rs146507421 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SNX9 | GRCh38.p7 | 6:157754764 | GCAGTGCAGGTGTTA[C/T]AGGAAAGGGGTCCTG | 51429 |
| rs146513520 | snp | A/C | 1.64893e-05 | 0.0028713 | missense | SNX9 | GRCh38.p7 | 6:157932210 | CATTACCCAAGGAAT[A/C]TCAGAAGATAGGAAA | 51429 |
| rs146540314 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157739948 | CACCAGGGCCCTGTC[A/G]GGCGGTGGGAGCCTA | 51429 |
| rs146589246 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157901203 | TACACAATCCTGCAT[A/G]CAATTTTGTATTTAC | 51429 |
| rs146592565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SNX9, LOC105378078 | GRCh38.p7 | 6:157884663 | TCATATACCAGTGTT[A/G]GAGGATTTATGGACA | 51429 |
| rs146593424 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SNX9 | GRCh38.p7 | 6:157841363 | ACAGATTTTATTACC[C/T]ACAGGCCCTGGGAGT | 51429 |
| rs146603641 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SNX9 | GRCh38.p7 | 6:157769799 | GTGTGTTGTGGGGAG[A/G]GATCTAGGCCACACA | 51429 |
| rs146607615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157771489 | TATAATATATATGTC[A/G]TAATTATTCAATAAC | 51429 |
| rs146625042 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SNX9 | GRCh38.p7 | 6:157737741 | TTCTTTTAATTGTGA[C/T]GTTAGGGTGTTGATT | 51429 |
| rs146661589 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157727928 | AAAAGACCGAAGCAG[A/G]GGTGTCTAATATTCA | 51429 |
| rs146679440 | in-del | -/AAATAAATAAAT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157769042 | AAGACTCCGTTCCAA[-/AAATAAATAAAT]AAATAAATAAATAAA | 51429 |
| rs146712313 | snp | A/C | 0.00953873 | 0.0683987 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822346 | CCAATTAAGACACAT[A/C]TTCCAGTCGTGTTTT | 51429 |
| rs146712681 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | SNX9 | GRCh38.p7 | 6:157866732 | GGCTAAAGATGCTGC[A/C]TTATCATTCTTATTA | 51429 |
| rs146717966 | in-del | -/CCCCCCCCCCCC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157757738 | GCAATGCCCCTTGCA[-/CCCCCCCCCCCC]CAGCCATACTGGGAA | 51429 |
| rs146731015 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157827831 | AGTCACCTTTAGGCT[A/G]ACTATAACAAGATTC | 51429 |
| rs146747962 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157724476 | TTGTTCTTTAAATGA[C/G]TAGGAGAGATCAGAG | 51429 |
| rs146818309 | in-del | -/ACATTCCTTGCAA | 0.0618563 | 0.164627 | intron-variant | SNX9 | GRCh38.p7 | 6:157785877 | GACTCTGGCTTAGTG[-/ACATTCCTTGCAA]ATATTCCTTGCAAAT | 51429 |
| rs146829982 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157863425 | AACAGATACGTGAGA[C/T]TGATGTCTAGTAGCC | 51429 |
| rs146830182 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | SNX9 | GRCh38.p7 | 6:157939553 | TGAGCTTTGAGGGCC[C/T]AAAGATGTGGTACTG | 51429 |
| rs146835567 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157923512 | AATGTACAAAAGATC[C/T]ACATAGAAAACTATG | 51429 |
| rs146849564 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157804430 | CTCCTCCTATGCATT[C/T]CTCTAGCTGGTTTCA | 51429 |
| rs146855062 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157881463 | GTGAAAGGAAGAGTC[A/G]CATTTCTCTCACTTT | 51429 |
| rs146868689 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157769547 | GGGGAAGACAGAGAG[A/G]AAGGGCGATTCAGGC | 51429 |
| rs146895566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157788482 | GCACAATTCTGAAGA[C/T]GGTTAACTTCTTTTA | 51429 |
| rs146915131 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157877580 | AACATTTTCCTATCA[A/G]GTTTGCCCATTGCTT | 51429 |
| rs146927688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157849213 | TCAGGTGATCATATA[A/G]TTTTTTAGTCCAAAC | 51429 |
| rs146955336 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | SNX9 | GRCh38.p7 | 6:157746269 | AATTCTTTTGTGAAG[G/T]CTTGCAACATGTGAA | 51429 |
| rs146962291 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157911666 | TCTGATCCCATAGCT[C/T]ACTCTGTTTCTGTTA | 51429 |
| rs146970264 | in-del | -/AAG | 0.244205 | 0.249933 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157892046 | CCATGATGGACAGTT[-/AAG]TAAGAGCTTTGCAAA | 51429 |
| rs146986405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886858 | ATTGATTTCATAATG[C/T]GTTTTGTTTTTTTTT | 51429 |
| rs146998179 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157772333 | ATTTGAAAATAGGGC[C/T]GGCCTTTGCAGATAT | 51429 |
| rs147002904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157891320 | AAGTGTGAACCGCTG[C/T]GCCTGGCCAAAAATC | 51429 |
| rs147025691 | snp | A/G | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157892961 | ACTGTGGCCCTCCGA[A/G]CCCCTCCATTTCACA | 51429 |
| rs147029744 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157833736 | TGCACTTCTCCTCCC[A/G]CCTTCCTAAACCATG | 51429 |
| rs147043289 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157729740 | GGATGGATCACCTGA[A/G]TTCAGTTCGAGACCA | 51429 |
| rs147060073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157732315 | ATCCCAGCTGGCTTA[A/G]GCCTGGGTCACCTGC | 51429 |
| rs147076194 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SNX9 | GRCh38.p7 | 6:157941565 | ATCTAGTAGCATGTC[C/T]CCCTCAGACACCTGC | 51429 |
| rs147088251 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157868237 | TATTCAAACAAGAAG[A/C]AACTCTATGTATAAA | 51429 |
| rs147092483 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157944067 | CAGCGCTTCACTTAA[C/T]GGCATAAAGCAAAAC | 51429 |
| rs147095248 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157908752 | CTCAAAACTTACACG[A/C]GGTCTCTACACCCCC | 51429 |
| rs147101690 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | SNX9 | GRCh38.p7 | 6:157759937 | CAGTGGTGTGAACTT[C/G]GCTCACTGCAACTTC | 51429 |
| rs147104700 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157828850 | CCGCCCCTGTTTCAG[A/G]GTCACATTACACACC | 51429 |
| rs147105155 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157873043 | CTCCACACAAAATTT[C/G]TCCAGGAAATCTCAA | 51429 |
| rs147118014 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157763745 | CCAAGGGGAGGTAGC[A/G]TGAAATGTTATCCTG | 51429 |
| rs147145651 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157933101 | AAAGGAACCCAGGCA[A/G]CATAAGGAGACCCCA | 51429 |
| rs147166926 | in-del | -/CTC | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888635 | CACCTTCTTCTCCTT[-/CTC]CTTCTCCTTCTTCCA | 51429 |
| rs147173520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157861443 | AGAAAGCGTGCTCAT[C/T]AGGCTTTCCGATGAC | 51429 |
| rs147175474 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157937222 | ACCAACTTAAAAATT[A/G]CATGATGTTTTGTTG | 51429 |
| rs147190477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157847190 | TCACTGCAGCTTCCA[C/T]CTCTTGGGCTCAGGT | 51429 |
| rs147190764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157798908 | AACTAGTTGGTTCTC[C/T]GTATTAGTCAGTTCT | 51429 |
| rs147193703 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157801970 | TCCACAATATTCAGT[C/T]CTCAAATACCTCAAA | 51429 |
| rs147205361 | snp | A/G | 0.030665 | 0.119967 | intron-variant | SNX9 | GRCh38.p7 | 6:157739326 | AGAATACATTTATGC[A/G]ACCAACAAACATATG | 51429 |
| rs147250650 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | SNX9 | GRCh38.p7 | 6:157915660 | ATATATATATATACA[C/T]ACACACACACAAAAA | 51429 |
| rs147280657 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | SNX9 | GRCh38.p7 | 6:157842975 | CAGAGTCAAACCATG[G/T]ATCAAATTCTTTCCC | 51429 |
| rs147280831 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157918951 | TACATTGTGGTAATT[A/T]CTGCTTTCTACAGTC | 51429 |
| rs147293864 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157781563 | GCTTAGTAAGACTAA[A/T]GCCTGAAATAATTGA | 51429 |
| rs147299118 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157903220 | CCAATTCCATGATTC[A/C]AGGCAGATATCAAAG | 51429 |
| rs147301787 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157860854 | CTAGAATTGTACAGT[C/T]GCCTTTTGTTACACT | 51429 |
| rs147312003 | in-del | -/AC/ACAC | 0.0574046 | 0.159605 | intron-variant | SNX9 | GRCh38.p7 | 6:157723064 | GCCCCTTGTATGAGG[-/AC/ACAC]ACACACACACACACA | 51429 |
| rs147317728 | snp | A/T | 1.64749e-05 | 0.00287005 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157909754 | CTCCAAAATGTATGG[A/T]CTAAAGAGCTACATC | 51429 |
| rs147342038 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157938059 | ATAGAGTTGTTCCTT[C/T]CAGACAGCGGTAAAT | 51429 |
| rs147349073 | in-del | -/ACTGT | 0.143622 | 0.226238 | intron-variant | SNX9 | GRCh38.p7 | 6:157867473 | ATGCTTAGAAAGTGA[-/ACTGT]AACTGTACACCTTTT | 51429 |
| rs147358139 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157897440 | TACATGTTCAGCACC[C/T]CAGAATCTCTTTTCC | 51429 |
| rs147374277 | in-del | -/CT | 0.030278 | 0.119257 | intron-variant | SNX9 | GRCh38.p7 | 6:157735244 | GGTGACAGAGCAAGA[-/CT]CTGTCTCAAAAAAAA | 51429 |
| rs147388191 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SNX9 | GRCh38.p7 | 6:157899986 | CAGCAGGTTTCCCAA[A/G]TATAATGCAATATCA | 51429 |
| rs147399202 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157768235 | CAGAAGACAAATATA[A/G]CAGAAGGAAAGAAAG | 51429 |
| rs147401935 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157839967 | CCTCTCCGGTTGTTT[A/C]ATGGTTTCACTAGGG | 51429 |
| rs147404397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157883241 | TTTTTTATACATAAT[A/G]CTCTCGCACACTTAT | 51429 |
| rs147407849 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157842271 | GTATGAGTCTGCCCA[A/T]GTTAATGTAAAACAG | 51429 |
| rs147415951 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | SNX9 | GRCh38.p7 | 6:157734825 | ATGAGGGAAAGAAAA[G/T]AAATTATATTTTCTC | 51429 |
| rs147417141 | in-del | -/ATA | 0.265453 | 0.249522 | intron-variant | SNX9 | GRCh38.p7 | 6:157859902 | ACTAGTGATTTTTAC[-/ATA]ATAATTTTGTTCCGG | 51429 |
| rs147418928 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157736764 | GCTTCCAGTTTTTGC[A/G]CATTCAGTATGATTG | 51429 |
| rs147503721 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157753832 | AGAAAGAGTAATATA[C/T]GCAGAGCCGGCTGTA | 51429 |
| rs147504186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157882429 | CTACAGCCCTTGGAT[C/T]GAGGAGTAATTTTGA | 51429 |
| rs147507828 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157819765 | CCCAGCTGTGTGGCT[A/G]GACGAAGCTTCCTGT | 51429 |
| rs147524157 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157722464 | CACAGGATGCTACGC[C/T]CTCTAGAATTATTTT | 51429 |
| rs147540148 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | SNX9 | GRCh38.p7 | 6:157725630 | CACAAGCAGCTGATG[A/C]AAGCAGTCAGGGATG | 51429 |
| rs147550162 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157853999 | ACCTATGTGCCTGGC[G/T]TCAAAGCCAGCTTAT | 51429 |
| rs147551408 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157929291 | TGTGCAGCTCTGTCA[C/T]CACACATGTGGCCCA | 51429 |
| rs147565418 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SNX9 | GRCh38.p7 | 6:157746273 | CTTTTGTGAAGTCTT[A/G]CAACATGTGAAGAGC | 51429 |
| rs147566554 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157811668 | GTTTTAAAAAGTCGG[A/G]GTCAAAGGTGATCCT | 51429 |
| rs147566802 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157858458 | AACTCCTGTACTCAC[A/G]TGATCCGCCTGTTTC | 51429 |
| rs147579183 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157750180 | AGACCCTGAATACCC[C/T]AATCTATCTTGAAAA | 51429 |
| rs147596211 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | SNX9 | GRCh38.p7 | 6:157815839 | TGGGAGGTGAACAAT[A/G]AGAACCCATGGACAC | 51429 |
| rs147653195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157924962 | GCTTACAGAAGATAA[C/T]GTGGAACATCCTCCT | 51429 |
| rs147655921 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157837129 | TGGGTTCATATGATG[C/T]AGAAAATCACAGATC | 51429 |
| rs147657692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157910240 | GAACGTTTAATGTGC[A/G]AATCACAGGTTTTGG | 51429 |
| rs147670022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157732478 | ATGTGATGACTCAAC[A/G]TACATTTACATTGTG | 51429 |
| rs147672310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157791842 | TCCAGTCAACATGAG[A/G]GATACCTATTGGTAT | 51429 |
| rs147686265 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157735419 | GACCTGGCCGGGCGT[A/G]GTGGCTCATGCCTGT | 51429 |
| rs147701570 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | SNX9 | GRCh38.p7 | 6:157795637 | TAGTTTTAAAATACT[A/T]CAGCAAAGGGGAACA | 51429 |
| rs147770343 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SNX9 | GRCh38.p7 | 6:157816765 | TGAAGCCCAGCACAT[C/T]GTTATAATAACTATT | 51429 |
| rs147772579 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | SNX9 | GRCh38.p7 | 6:157773689 | CCAAGATCAGGGAGG[A/C]GGCAACTGGGATGGG | 51429 |
| rs147773165 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | SNX9, LOC107986663 | GRCh38.p7 | 6:157714348 | AACTAATTGGGAATG[C/T]GTGACTTCAATAAAC | 51429 |
| rs147773395 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SNX9 | GRCh38.p7 | 6:157820392 | CTTGAACCTGGGAGG[C/T]GGAGGCTGCAGTGAG | 51429 |
| rs147789192 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157778247 | CACTGTGAATCTATT[C/T]GTGCCCAAATTGCCA | 51429 |
| rs147818175 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157731832 | GCTTGGAGCCCAACT[A/G]GGTTTCCTATTGGAG | 51429 |
| rs147860700 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885601 | CCTAACACAGTTGCA[C/T]GTGGTATAGTCGTAA | 51429 |
| rs147862685 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157934450 | CTAATCAAAAGCAAA[A/G]TAAAACAAATGATAC | 51429 |
| rs147863513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157871096 | GATTGAAAAAAGAAT[C/T]GGCCAGGTGCAGTGG | 51429 |
| rs147877177 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157763695 | ATGTTTCTCATGTGC[C/T]TGCCTGTCTGTCCTA | 51429 |
| rs147880772 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157877574 | TTTTTAAACATTTTC[C/G]TATCAGGTTTGCCCA | 51429 |
| rs147894367 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | SNX9 | GRCh38.p7 | 6:157765209 | GATCTGATCTCCTCC[A/C]CAAAGAGTTAGATGG | 51429 |
| rs147910141 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | SNX9 | GRCh38.p7 | 6:157836685 | AAACTCCGCCTCCCA[C/G]GTTCACGCCATTTTC | 51429 |
| rs147950208 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | SNX9 | GRCh38.p7 | 6:157910904 | AGGCGGGCGGATCAC[A/G]AGGTCAGGAGATCGA | 51429 |
| rs147960582 | in-del | -/AT | 0.0448719 | 0.142907 | intron-variant | SNX9 | GRCh38.p7 | 6:157903268 | GGAAAAATTAAAAAC[-/AT]AACATTTGACATATA | 51429 |
| rs147967148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157867149 | GTAGAGATGGAATCT[C/T]GCTTTGTTGCTCAGG | 51429 |
| rs147986764 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157770097 | TGCCCAGGGCTGAAC[A/G]TTTTCCACAGATCTA | 51429 |
| rs147991376 | in-del | -/G | 0.0103295 | 0.0711199 | intron-variant | SNX9 | GRCh38.p7 | 6:157898527 | TTGAGCCAGAAACGT[-/G]TATGTGGATGGGATG | 51429 |
| rs148012710 | snp | C/G/T | 4.95081e-05 | 0.00497514 | missense | SNX9 | GRCh38.p7 | 6:157942821 | AGGCAGGCCCTCAGC[C/G/T]GCTTTCCAGTGATGT | 51429 |
| rs148016605 | snp | A/T | 0.021333 | 0.101051 | intron-variant | SNX9 | GRCh38.p7 | 6:157736371 | GAAGAGGTCCTTCAC[A/T]TCCCTTTAAGTGGTA | 51429 |
| rs148020677 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157829603 | TCTACTTGATGGTGA[C/T]GCTAAAATGGTGAAT | 51429 |
| rs148021204 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157814043 | CTTCCAGTAAATGTT[A/T]TTTAACAGTTCCAAG | 51429 |
| rs148025057 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887069 | GATAAATTATGAGTG[C/G]ATGTCAGACATTGCA | 51429 |
| rs148032883 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157724778 | GGAACATTGACTTTC[A/G]TTCTTTGGAATCTGT | 51429 |
| rs148100820 | in-del | -/ATA | 0.00953873 | 0.0683987 | intron-variant | SNX9 | GRCh38.p7 | 6:157862249 | ACATATGTTAATAGC[-/ATA]ATAATGCTCAGGGTC | 51429 |
| rs148114673 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157930055 | CAGAAACTTGTGGCT[C/G]CATAAAGCCTAAAAC | 51429 |
| rs148142960 | snp | C/G | 0.143959 | 0.226396 | intron-variant | SNX9 | GRCh38.p7 | 6:157858354 | CGGGTTCAAGTGATT[C/G]TCCTGCCTCAGCCTA | 51429 |
| rs148144320 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | SNX9 | GRCh38.p7 | 6:157796322 | AGACCAGAGAAGAGA[C/G]GTGTGAGTCAGGACA | 51429 |
| rs148176278 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157763785 | TGTGAGTTAGAAAAC[A/G]TGGCCAAGTGCCCCC | 51429 |
| rs148180670 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157845819 | TGGTTCTTGTGAACT[A/G]AATATTGGACTTTGA | 51429 |
| rs148231165 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157789606 | TCTGACTGCCATTTA[A/T]CAGCTGTGTGACCTT | 51429 |
| rs148232475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157864984 | AGTGAGCTGAGACTT[A/G]CCACTGCACTTTAGC | 51429 |
| rs148235187 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157774817 | GAGAGGGAGAGAGGG[A/G]TCACACTTCTTCCCA | 51429 |
| rs148236229 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157851612 | TTTTTCTTTTTGAAA[C/T]GGAGCCTCACTCTGT | 51429 |
| rs148251890 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157743918 | GCTACTCGGGAGGCT[G/T]AGGCAGGAGAATCGT | 51429 |
| rs148270800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157913764 | CAGTGTATAGTCTTT[C/T]GAGTCTGACTGCTTT | 51429 |
| rs148295931 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157721990 | TCGAGGGGAAACCAG[A/C]TCTCCTAAGTCCTCC | 51429 |
| rs148337772 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893582 | TTCTTGCAATTATAT[A/T]TTTTTCTTTTTTTAA | 51429 |
| rs148368478 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157732874 | TTGGCCCAACATCTC[C/T]CCATTTCTGCCATCC | 51429 |
| rs148372554 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157941413 | AGGTTTTCACAGTGC[A/G]CCATGGAAATCGCAG | 51429 |
| rs148388547 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157899218 | CTTCACTCTCATCTT[C/T]TTCTCCCACACCCCA | 51429 |
| rs148436624 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157761616 | CAGGATATGGAAAGG[C/T]GGCCTAGAAGCAAGT | 51429 |
| rs148478099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157876429 | GTACTCCAGCCTGGG[C/T]GAGTGAGACTCCTCA | 51429 |
| rs148481939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157862339 | AAGACGTTAAATATT[A/G]TACAATTTTGTAAGT | 51429 |
| rs148493390 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157764640 | TCCCCTGGAGCTGAC[C/G]ATGAATCACTTCTCA | 51429 |
| rs148498680 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157848085 | TTGCACTCACCACCA[C/T]CTGGAATTGCTTTGC | 51429 |
| rs148509051 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157716675 | TTTGTTTTGTTTTTT[C/T]CTTAGTGCATTACAT | 51429 |
| rs148528425 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157803025 | GATGGCTGGAGAGAA[C/G]GTAGTTTCTGACTCA | 51429 |
| rs148533165 | snp | A/G | 0.000153988 | 0.00877328 | missense | SNX9 | GRCh38.p7 | 6:157910022 | CCAGACAAACAAGTC[A/G]CAGGTGAGTGTGTGT | 51429 |
| rs148533918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157909345 | CTAGTCCTTCATCAC[A/G]TGTAGCTTGAGACAG | 51429 |
| rs148549146 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157756089 | ATTTCTATTTTATTT[A/C]ATTAATACCATCCTC | 51429 |
| rs148553143 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157853014 | TTTGTTTGTTTGTTT[A/G]TTTTGCATGGCCCAT | 51429 |
| rs148603822 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157781852 | TGTGTGCATATGTGC[A/G]GTGTAGGGCATCAGA | 51429 |
| rs148649639 | in-del | -/TTTA | 0.132066 | 0.220435 | intron-variant | SNX9 | GRCh38.p7 | 6:157913301 | ACTATCTATCTATAT[-/TTTA]TTTATTTATTTATTT | 51429 |
| rs148684243 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157839885 | TGCGCAGTATTGGGG[C/T]GTGAATCTCTGCAAA | 51429 |
| rs148689068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157942646 | TCTGTCCAGCAGCAA[C/T]GCGGGGCAGGGCTGG | 51429 |
| rs148697826 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157734673 | CAAGGTCCGAAGGCC[A/C]CTGCCTTGAGAGAGA | 51429 |
| rs148710564 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157883657 | AGGCAAACTGATGAT[C/T]CTCCAAATATGTCCC | 51429 |
| rs148739824 | snp | A/C/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157843129 | GTGGTTTCAAGGAGA[A/C/T]GAAGCCTTCTAAGCC | 51429 |
| rs148761551 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157815354 | CCTCCCAAGTGGCTG[A/G]GACTCCAGGCACATG | 51429 |
| rs148768140 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157726992 | AGGTCACTCTAGTTC[A/G]GAGGTGAGGCTTCAA | 51429 |
| rs148776110 | in-del | -/TGTCA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157914454 | AGCTGTGGCTTGGCT[-/TGTCA]TTTTCTTTTTCTTTT | 51429 |
| rs148811426 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157754226 | AAAGGCAATCTAGTC[A/T]CCAAGCAAGAAGGAG | 51429 |
| rs148825841 | snp | C/G | 4.95528e-05 | 0.00497734 | missense | SNX9 | GRCh38.p7 | 6:157938637 | ATATTTCACAGGGAG[C/G]AATAGAAAAAGTGAA | 51429 |
| rs148827764 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157719962 | CACTTGAACCTGGCA[C/G]ATGGAGGTTGCAGTA | 51429 |
| rs148832512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157924215 | TATATATAAATATAT[A/G]TATGTATGTATTATA | 51429 |
| rs148848571 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157805330 | AGGTTCTCATCGTCT[C/G]TCACCTGGACTCTTA | 51429 |
| rs148849266 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SNX9 | GRCh38.p7 | 6:157882138 | TTGAAACCAGTGCTC[A/G]TTTACCATTCTGAAA | 51429 |
| rs148852367 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157769895 | GAAGGAGAGCACCAG[C/G]GGTCTGAAAGCAGAA | 51429 |
| rs148865011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157758254 | GAAAGAAAAAAGAGA[A/G]GAAGGAAGGAAAAAG | 51429 |
| rs148879451 | snp | C/T | 1.66283e-05 | 0.00288338 | stop-gained | SNX9 | GRCh38.p7 | 6:157873147 | AACATCAAAGGAGAA[C/T]GAGGGCTGGTTCCCA | 51429 |
| rs148883901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157854552 | TACATGCAAACACGT[A/G]TGGCAAATTTATAAC | 51429 |
| rs148900182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157813539 | AAAGGGGTCAGCAGC[A/G]CCTCTCCTCATTCCT | 51429 |
| rs148938573 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SNX9 | GRCh38.p7 | 6:157859927 | TTCCGGGTCATGTTA[G/T]AGGAGTCAGCAAATT | 51429 |
| rs148958248 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157866745 | GCATTATCATTCTTA[C/T]TAGATAAGGAGCAGT | 51429 |
| rs148966750 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157791140 | AGGTTTTTGAGTGAG[C/T]ATCTGTCAGATTCTT | 51429 |
| rs149004684 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SNX9 | GRCh38.p7 | 6:157841126 | CTGGGGCAGAATGCT[A/G]TTATGGGCTAAGAAG | 51429 |
| rs149006030 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | SNX9 | GRCh38.p7 | 6:157916045 | TCTTTTCTTTTTTTT[G/T]TTTGTTTGAGACGGA | 51429 |
| rs149007961 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157795966 | TTAAATTTAAAACTA[C/T]GAACAAAATCAGTAT | 51429 |
| rs149013129 | snp | A/G | 0.0254324 | 0.109861 | intron-variant | SNX9 | GRCh38.p7 | 6:157902057 | ACAAGTAAGTTTAAA[A/G]GGGAGCCAGGGAACC | 51429 |
| rs149019716 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | SNX9 | GRCh38.p7 | 6:157736069 | AGAGACACTTGTATT[G/T]GGATTTTGTTAAGTA | 51429 |
| rs149037394 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157818513 | GTTTTAACCATCACA[G/T]TTTGTAACTTGAGCA | 51429 |
| rs149040285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885304 | TTCATTTTTAGAAGA[A/G]TGTACAAGTTTTATG | 51429 |
| rs149055991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157845452 | TACACTTATTTTGAC[A/G]GTAAACTTTTTAGCC | 51429 |
| rs149072610 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157728836 | AGGGCACAGTGGCTC[A/G]TGCCTGTAATCCCTG | 51429 |
| rs149095496 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893162 | AGAAAACTGTAGAAG[A/G]AAGGGTTTCTCTTAG | 51429 |
| rs149106771 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157774644 | GCTGGGAGGAGCGCC[A/G]GATCACATTTCCTCT | 51429 |
| rs149154308 | in-del | -/CTCTGCA | 0.0532157 | 0.154195 | intron-variant | SNX9 | GRCh38.p7 | 6:157756372 | GAGCTGTGATTGTTC[-/CTCTGCA]CTCTGCACTCTAGCT | 51429 |
| rs149156684 | in-del | -/CT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157870609 | CACACCCCTCAGACA[-/CT]CTCACCTGCCCTCAC | 51429 |
| rs149165284 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157831744 | AGCAGTGTGTTTCAA[A/C]AGGTGTTTAGTTTGT | 51429 |
| rs149171167 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157935216 | GAAAGTTGATCCTTA[C/T]GGAAGTATTTCAGCT | 51429 |
| rs149178176 | in-del | -/TGT | 0.0726307 | 0.176182 | intron-variant | SNX9 | GRCh38.p7 | 6:157792935 | ATCACTGGGTTTTTC[-/TGT]TGTTGTTGTTGTTGT | 51429 |
| rs149192172 | in-del | -/T | 0.0460142 | 0.144533 | intron-variant | SNX9 | GRCh38.p7 | 6:157913227 | TGGTGTCTAGACTCA[-/T]TGTTCTGTTCAAGTC | 51429 |
| rs149211369 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157808078 | TCAGGAAAAAAAAAA[-/A]TCCTAAAGAAATGAG | 51429 |
| rs149217844 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157877662 | GGAGGCTCTGATTGC[C/T]TGTGCTCTCTCCCAG | 51429 |
| rs149221436 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157837420 | TTATATAATGAAAAT[A/T]ACTTTTAATTCACTA | 51429 |
| rs149222863 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157864088 | GAACAGAATTTATTC[A/C]TCATAACTGTGGAGG | 51429 |
| rs149223896 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157941228 | GGCCCCAAGAAGTTC[A/C]TTATTGTGCAGCTCC | 51429 |
| rs149229685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157765795 | ATCCTGACCCTCCTG[C/T]TGTAATATTTATTCA | 51429 |
| rs149238573 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | SNX9 | GRCh38.p7 | 6:157904348 | CTCAGGCAGGAGAAT[C/T]GCTTGAACCCGGGAG | 51429 |
| rs149258544 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157911037 | AGAATGGCATGAACC[C/T]GGGAGGCAGAGGTTG | 51429 |
| rs149275257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157868840 | AAAACTTGAACCCAT[C/T]GTTACCTGCTTTCTT | 51429 |
| rs149282347 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157852588 | GCTACTTTTTTGTTT[G/T]GTTTTTTTGAGACAG | 51429 |
| rs149300619 | in-del | -/A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157729557 | GAATGTAGAATATAA[-/A/T]AAAAGATAGAATTTC | 51429 |
| rs149313757 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157917923 | ATTTCCAACTATCTG[A/G]CCATTTCCTGAATTT | 51429 |
| rs149317543 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157747103 | GCTCACTTGTCCGCC[A/G]CTCACCTCCTGCTAT | 51429 |
| rs149322576 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157842197 | AAGTTTGCTGTATCT[A/G]TTAAGTTGCTTGATA | 51429 |
| rs149325694 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157798207 | AATGGAAATTTTATA[C/G]CCCCTGTGAGGGCGC | 51429 |
| rs149361846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888948 | AGGAGTGTGGTACCA[C/T]GGAGAGAGGGAAAAG | 51429 |
| rs149364857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157847738 | TAGTAGTGCTAAAAT[C/T]CTGTAACATATTTTT | 51429 |
| rs149371538 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | SNX9 | GRCh38.p7 | 6:157752881 | CAGAGGTCCCTGCGG[C/T]CTTCCGCAGTGTCTT | 51429 |
| rs149373846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157772576 | TCCCCAGAGCCTCTG[A/G]GGAGAGCATGGCCAC | 51429 |
| rs149397181 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SNX9 | GRCh38.p7 | 6:157730698 | AGGCTGGAGTGCAGT[A/G]GTGCAATCTCGGCTC | 51429 |
| rs149397928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157936936 | ATGCACACATGTGTA[C/T]ACACACTAATGTGGT | 51429 |
| rs149412093 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157788847 | ATTTAATAGCTGTAT[A/C]ACTGTGGGCAATTTA | 51429 |
| rs149414581 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157896104 | TCGTTCTAGATTGTA[A/G]GAAGGAGGCTGCCCA | 51429 |
| rs149448468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157734147 | ATACATAAATGAAGA[C/T]GGAAAACAAATACAT | 51429 |
| rs149454068 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157942045 | TTGATTTATTGATTT[G/T]CAAGTCCAGGTATGG | 51429 |
| rs149487531 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157730213 | ACTGTTTTTTTTTTT[A/T]TAAAAAAAAAAAAAA | 51429 |
| rs149523453 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157879033 | GCTAGTGTCATACAG[A/G]TGTGGTCAGACAGGC | 51429 |
| rs149532893 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | SNX9, LOC107986663 | GRCh38.p7 | 6:157715116 | GTCCCATAGAACCAC[A/G]CCCTTACCCAGGCTG | 51429 |
| rs149537047 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157767655 | TGAAATTTGCATTCA[A/G]TGCAAGTTAAACGGA | 51429 |
| rs149540633 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157839641 | CATCCCCGTCCTGCT[A/G]GGGAAGCAGACCTAT | 51429 |
| rs149553014 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SNX9 | GRCh38.p7 | 6:157755327 | CGGGAGAAATTCTCC[C/T]TCTCAGCCATCTCTT | 51429 |
| rs149574844 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157926868 | GAGAACATGGCTGAA[C/T]TGGTTCATTCTTTAA | 51429 |
| rs149578109 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157883401 | TTTAAGAAACTTCAG[A/G]GTCTCCTCTATTGCC | 51429 |
| rs149582408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157721367 | TCATGCTAATCTTAA[C/T]GGATAGGCACCATCA | 51429 |
| rs149587556 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157809090 | GTCTTCCCATTAAAA[A/G]GAAAGCTTAGGCCTT | 51429 |
| rs149625946 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157858167 | GTGCTTTTCATGCCT[A/G]TGTTAGTATCACATA | 51429 |
| rs149626100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157932454 | ACTTTTGAGAAAAGC[C/T]AAAGGTGGTTATAAT | 51429 |
| rs149633438 | snp | C/G | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157892962 | CTGTGGCCCTCCGAG[C/G]CCCTCCATTTCACAG | 51429 |
| rs149675868 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157786069 | TAAGAGACAGACAGG[A/G]TCTCAGTCTGTCAGC | 51429 |
| rs149677003 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157861978 | TCAGGTGGGCAGTGT[C/T]TATGGTGTAGAGATG | 51429 |
| rs149684099 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SNX9 | GRCh38.p7 | 6:157849125 | AGAAAAGAAAAGAAA[A/G]TAGTTCAATAAGTCT | 51429 |
| rs149686062 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | SNX9 | GRCh38.p7 | 6:157924014 | ACCAGCCAGGCCAAT[A/G]TGGCGAAACCCTGTC | 51429 |
| rs149689929 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157754039 | GCCACAAGATCAGGT[C/G]AGCCAGTTTATTGAT | 51429 |
| rs149713097 | snp | A/G | 4.95544e-05 | 0.00497742 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157867597 | AAATAATGAACTGAC[A/G]GTTAATGAAGGAGAA | 51429 |
| rs149715485 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | SNX9 | GRCh38.p7 | 6:157909097 | AATGACTATCAGGCT[C/G]TGGCCAATCTGATTA | 51429 |
| rs149720565 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157898330 | TTGGTAAAGTAAAAG[A/C]AGAATGGGCGGTGGA | 51429 |
| rs149727756 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | SNX9 | GRCh38.p7 | 6:157790992 | TCATCATTGTTGGAA[A/C]GGTTTGGGAACCCAC | 51429 |
| rs149728058 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157731734 | AAGAATAATCTGCCG[A/T]TCTATTACAAAAATC | 51429 |
| rs149753238 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157750268 | AAAGTTCTGATAATT[-/A]AAACACTATGGTATT | 51429 |
| rs149766799 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157840268 | ACAGTGAGGCCAGAG[C/G]TGAGGGAGCTCAGGG | 51429 |
| rs149781804 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SNX9 | GRCh38.p7 | 6:157735563 | AAAGCCCAGACCTTC[A/G]CAAGTCTGAGGCAGA | 51429 |
| rs149803634 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SNX9 | GRCh38.p7 | 6:157836619 | TTTTTTTGATACAGA[A/G]TCTTACTCTCGCCCA | 51429 |
| rs149842647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157881021 | TAAAACAAGACATTA[A/G]GGACAGGCACACTTC | 51429 |
| rs149849248 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157777129 | GGGTATGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 51429 |
| rs149878541 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157929156 | CCGAGGGGAGAGTGT[C/T]GCTGTCAGTCACGGC | 51429 |
| rs149894483 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157811509 | GAGGCTAATTGCTAC[A/G]AATGCAGTGTAAGAT | 51429 |
| rs149894972 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | SNX9, LOC105378078 | GRCh38.p7 | 6:157884930 | ATACGTACATCCTGT[C/T]ATCAGCACAGTGTAA | 51429 |
| rs149904253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157723639 | AGAAACTGCTGAAGC[A/G]TGGCAAGCTTGTCTT | 51429 |
| rs149933772 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157934587 | ATGTTAGTTGTTTTC[A/T]CTAAACATGTAGTCA | 51429 |
| rs149937719 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157763238 | GTAGGGGCTGGGGCT[C/T]CTTGGGTACAAGGCA | 51429 |
| rs149942067 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157831446 | AGGAGAAATTTTCCT[C/G]ATCCCCACTACTCTG | 51429 |
| rs149954443 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157728466 | TTCGACCTTTGCCTT[C/T]GCATCTCCCCTTGGG | 51429 |
| rs149977425 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157877617 | TCTGAATGCGGGTAG[A/G]AAGATGTGTGCTCTG | 51429 |
| rs149990954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157765379 | TTTGTTTTCTGAGAC[A/G]GAGTCTCGCTCTGTC | 51429 |
| rs150002178 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157781818 | TATCACAAAGTGTAT[A/G]TGTGTGTGTGTGTGT | 51429 |
| rs150019422 | in-del | -/CCAAAA | 0.0279526 | 0.114869 | intron-variant | SNX9 | GRCh38.p7 | 6:157903192 | AAATTACTAATACTT[-/CCAAAA]TTTCCCAATATTCCA | 51429 |
| rs150050170 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157815312 | CGGATTCCTGGGCTC[A/G]AGCAATCCTCCCACC | 51429 |
| rs150067365 | snp | A/G | 0.0785177 | 0.181917 | intron-variant | SNX9 | GRCh38.p7 | 6:157799568 | TTTCACACTGCTGAT[A/G]AAGACATACCCGAGA | 51429 |
| rs150087476 | snp | G/T | 0.000198 | 0.00994791 | missense | SNX9 | GRCh38.p7 | 6:157932262 | AGTGTTCAGTTCCAG[G/T]GGCTATCAAGGTGCG | 51429 |
| rs150120002 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157740936 | CAGTTTCAAAATGGA[A/G]GGAATGACATCTACT | 51429 |
| rs150153985 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157779739 | ATGTGAAGTACCTGA[A/T]GTAACAGATATTTGA | 51429 |
| rs150158257 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157854512 | CTAATTGCTTCTGTG[C/T]ATGTGTGTGCTTTGA | 51429 |
| rs150159552 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157882753 | AATTTCTTCAACCTC[A/G]TGATAAAACTTGAAC | 51429 |
| rs150170691 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157746407 | AACAGTTAAGGTGGG[C/G]AGTCTGTAGCCTACA | 51429 |
| rs150190610 | snp | A/T | 0.00953873 | 0.0683987 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157943146 | TGATATTTTACATAG[A/T]GTCATAATTTATATG | 51429 |
| rs150205007 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157828668 | CCAGCTACTTTTTGT[A/G]TTTTTTGTAGAGATG | 51429 |
| rs150207062 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | SNX9 | GRCh38.p7 | 6:157783935 | GGCGTGAGCCACCGT[A/G]CCCAGCCAATACCTC | 51429 |
| rs150207899 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | SNX9 | GRCh38.p7 | 6:157725092 | TGGTTGACTTTTTTT[C/T]CCCGATACTTCAGAT | 51429 |
| rs150227238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888363 | TTAATACTGTATCAT[A/G]ATGCCAAACAACAGA | 51429 |
| rs150243111 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157874922 | GAGTATGCGGCAAAA[A/G]CAGTGCTTACAGAGA | 51429 |
| rs150246575 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157834869 | CAACAGTATGTAAAG[C/T]GTATTCAATGTCCTT | 51429 |
| rs150293774 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157801215 | ACAGACGGGCTTCTG[A/C]TCTTCTTCACTTCTT | 51429 |
| rs150327449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157771654 | TCGCCCAAGATGCAC[A/G]CAGGAGGAGCTGCCA | 51429 |
| rs150361615 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157858987 | AACCATATCACATAC[A/T]CTCCATTTTTTCCAA | 51429 |
| rs150365052 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157817307 | CAAGGATGCCTGATG[A/C]CACGACCAAGGCCAT | 51429 |
| rs150400567 | in-del | -/AAATAAATAAATAAATAAAT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157769042 | AAGACTCCGTTCCAA[-/AAATAAATAAATAAATAAAT]AAATAAATAAATAAA | 51429 |
| rs150400863 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157905605 | AAGAGACTTGTTTTC[C/T]GCTGTCATGAACTGC | 51429 |
| rs150403625 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157863878 | TTTTATTGACATGTT[A/G]TACTTATTTGGAGAT | 51429 |
| rs150412843 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157787808 | CCAACTCCTTACATA[C/T]TCTTAAGCTATAAAT | 51429 |
| rs150436610 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | SNX9 | GRCh38.p7 | 6:157926585 | ACAGGAGTTCAAGAC[C/G]AGCCTGGCTAACACA | 51429 |
| rs150450842 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157805093 | GAGTCATGTAAGCAT[C/G]GTTTTATGACTGGAT | 51429 |
| rs150451953 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157838453 | TCCATTAGGTGTACG[A/G]TTGCTGTGGTAAAAG | 51429 |
| rs150452969 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157910938 | CATCCAGGCTAACAC[A/G]GTGTAACCCTGTCTC | 51429 |
| rs150464063 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157732968 | CATTTAAGTGAGATC[A/G]TACAGTATGTGTCTT | 51429 |
| rs150472202 | in-del | -/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157774237 | GGAGGAGGTGGAGGA[-/G]AGTGGAGGAGGTGGG | 51429 |
| rs150493672 | in-del | -/TT | 0.0494327 | 0.149241 | intron-variant | SNX9 | GRCh38.p7 | 6:157757267 | TTGAGCCCCATACTC[-/TT]TGTATGAGGTATGGG | 51429 |
| rs150496481 | snp | A/C | 0.00159617 | 0.0282053 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157945050 | GAGCTGTAGTCATAC[A/C]ATCACATAACTTTTA | 51429 |
| rs150512917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157830073 | CCCCCAATATGATCA[A/G]TTATTGCCCAGTATT | 51429 |
| rs150521747 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | SNX9 | GRCh38.p7 | 6:157736578 | ATGGGGTTTTCTAAA[C/T]ATACAATCATGTCAT | 51429 |
| rs150524565 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157727116 | TAATTAAGGCAAAAG[A/G/T]TCGAGGGAAGGGAGA | 51429 |
| rs150529285 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157785686 | TGGTGATTTACTGAA[C/T]ACTTGCCCCATAAGA | 51429 |
| rs150556098 | in-del | -/AT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157818103 | CACACACACACACAC[-/AT]ATATATATATACATA | 51429 |
| rs150558936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157772462 | AGGGATGAAGGCCAA[A/G]TGAAAAGGGAGGCAG | 51429 |
| rs150560983 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157876598 | AAATTTGCAGGCAAG[A/G]TGATTGATCACTGTA | 51429 |
| rs150564374 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157764854 | AGCTCCTGCCTTGCA[A/T]CACTGAGCTGGAAAA | 51429 |
| rs150564881 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157836271 | TCTTGTGCACGTTCT[C/G]GAGTTTTCATTATGA | 51429 |
| rs150590221 | in-del | -/AG | 0.0103295 | 0.0711199 | intron-variant | SNX9 | GRCh38.p7 | 6:157901822 | TAGGTAGTTACTGTC[-/AG]AAAATTAAGTAATTT | 51429 |
| rs150603121 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | SNX9 | GRCh38.p7 | 6:157880764 | TCCTTAAGAGGCAAC[C/G]TAGCTTGGTGTCAAG | 51429 |
| rs150609152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157776018 | CAGAGAAGATACATT[C/T]AGCCAGAGTTAAGAT | 51429 |
| rs150662662 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157723582 | ATCATTCAGGCTCAG[C/G]CCTTGGAGGTTTTCT | 51429 |
| rs150670755 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157936314 | GTGAATCTCTTGAGT[C/T]CAGGAGTTCGAGACC | 51429 |
| rs150685635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157818992 | CTGGACACTATGTCC[C/T]GTTACTGTTTACGGC | 51429 |
| rs150697241 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157828513 | TTATTTTTTTTTTGG[A/G]GACAGGGTCTCACTT | 51429 |
| rs150697309 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157717577 | GGTAGGAAGCATCCA[A/G]AAGGAAACCAGGTTG | 51429 |
| rs150720651 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SNX9 | GRCh38.p7 | 6:157865194 | AAATATGAAAATTAG[C/T]CAAGTGTGGTGGTAG | 51429 |
| rs150724960 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157941964 | CATTGTATATTAGAA[C/T]ATAACAGATTACATT | 51429 |
| rs150737199 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157825580 | CCACTCCAAAGGCAA[A/G]TTCCAGTAGTTCTGT | 51429 |
| rs150737521 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157756215 | GTCAGGAGTTCAAGA[C/T]CAGCCTGGGCAACAT | 51429 |
| rs150759822 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SNX9 | GRCh38.p7 | 6:157914180 | GTTTTTCCTCATTTT[A/G]ACCAGTCCGATAGGT | 51429 |
| rs150767460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157808888 | AAAAGAGAGGACATC[A/G]CTAATGATTTTATAG | 51429 |
| rs150776439 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157869474 | TATTTCTGTTGTGGC[G/T]CCTTTCCATTCAGTG | 51429 |
| rs150798579 | in-del | -/TGTT/TGTTTGTT/TGTTTGTTTGTT | 0.004783 | 0.0487016 | intron-variant | SNX9 | GRCh38.p7 | 6:157919953 | AAGTTCAGTTATTGC[-/TGTT/TGTTTGTT/TGTTTGTTTGTT]CTGTTTGTTTGTTTG | 51429 |
| rs150811903 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157919055 | ATATTTCCGGTGCTG[C/T]TTATTTGTCTCTGCA | 51429 |
| rs150820652 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | SNX9 | GRCh38.p7 | 6:157748560 | ATAGTGAAACCCCAT[C/T]TCTACTAAAAATGCA | 51429 |
| rs150824206 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SNX9 | GRCh38.p7 | 6:157843929 | ACCCAGGCCAGAGTG[C/T]AGTGGCATGATCTTG | 51429 |
| rs150843470 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157851748 | GCGTTCGCTACCACA[C/T]CCAGCTAATTTTTTG | 51429 |
| rs150874936 | snp | A/G | 0.000644101 | 0.0179342 | missense | SNX9 | GRCh38.p7 | 6:157902015 | GAAACAGTCGTGCTA[A/G]TTCCTCATCCATGAA | 51429 |
| rs150882532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157899588 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCATCT | 51429 |
| rs150897517 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157781177 | GTTTTTCAAGGTCAA[A/G]AAAAAAATAGTCAAC | 51429 |
| rs150912990 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157857098 | ATTTCCTACCATTCT[A/G]TAATGATGACCAATT | 51429 |
| rs150925896 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157720127 | ATTAGCATGTCTGGT[C/T]GCAAGGTTTGCTATA | 51429 |
| rs150931232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157779003 | CCTGTCACAATCCCT[A/G]TCTAGGAGTTACTAG | 51429 |
| rs150966585 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890761 | GGAGCTCAGACGAGA[A/G]TGATTGTATATGTCG | 51429 |
| rs151021517 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157898160 | CACAATACCACTCTG[A/G]GTCATTGAGTTGAAA | 51429 |
| rs151033818 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157803566 | GAAAATAACAAAGAC[A/G]CATAATGAGCAGGAA | 51429 |
| rs151042891 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157866881 | ATGAACAGTTTGTGT[A/T]TTTCCACTTCTTACC | 51429 |
| rs151044085 | in-del | -/AT | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157895101 | GTGCAGTAGGTAAAC[-/AT]ATGTAACATCCATCC | 51429 |
| rs151057082 | snp | A/G | 0.000494862 | 0.0157221 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157942863 | GGCCTTGAAGAGAAT[A/G]CCGCGTGCTTTCTCC | 51429 |
| rs151064442 | snp | A/G | 8.24137e-05 | 0.00641873 | missense | SNX9 | GRCh38.p7 | 6:157921600 | TGACCAGGATGTGTC[A/G]CCATCCAGTAATCTC | 51429 |
| rs151078968 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SNX9 | GRCh38.p7 | 6:157916144 | GGTTCACACCATTTT[C/T]GTGCCTCAGCCTCCC | 51429 |
| rs151084707 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157745557 | GGAGCCAAGAAAAGA[A/C]GACTTGATCCTTCGT | 51429 |
| rs151095446 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | SNX9 | GRCh38.p7 | 6:157874536 | GCAGGCAGAAAATCA[G/T]TAAGGACGTGGTTGA | 51429 |
| rs151167347 | in-del | -/TTTTG | 0.146314 | 0.227484 | intron-variant | SNX9 | GRCh38.p7 | 6:157852580 | TCCTATGTGCTACTT[-/TTTTG]TTTTGTTTTTTTGAG | 51429 |
| rs151179092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157853342 | TATGTAATAATATAT[A/G]TTTTTCTCCTTTCTC | 51429 |
| rs151179291 | snp | C/T | 0.0134377 | 0.0808595 | missense | SNX9 | GRCh38.p7 | 6:157928667 | TGAAGGAGCTGCTGA[C/T]GGTGGGGCAGGAGCA | 51429 |
| rs151200529 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | SNX9 | GRCh38.p7 | 6:157900853 | TGGTTACAAACAATC[C/T]GTAGAAACAGGACGT | 51429 |
| rs151215302 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SNX9 | GRCh38.p7 | 6:157763081 | CACAGATTATACGTC[C/T]CAATGTAAAACACGA | 51429 |
| rs151230834 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157858788 | CTTACATGGCAGCAG[A/G]CAAGAGAGCTTGTGC | 51429 |
| rs151250061 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | SNX9 | GRCh38.p7 | 6:157737587 | TATCTATTTTGTTAA[C/T]CTTTTCAAAAAACCG | 51429 |
| rs151250787 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157799333 | GTGTGGAGAGGTATG[A/T]GTACATGCACACTTA | 51429 |
| rs151252086 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157833302 | AAAAAGATTTTTTTT[A/T]AATTAAAAACTTACT | 51429 |
| rs151265105 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157729527 | TAGGCAGCAGAGAGC[A/G]CTGACATATATAATA | 51429 |
| rs151265155 | snp | C/T | 0.000181706 | 0.00952994 | missense, utr-variant-5-prime | SNX9 | GRCh38.p7 | 6:157867550 | CACTCCTGATAGGCT[C/T]GGGTTATGTATGATT | 51429 |
| rs151281242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157787483 | TGTGTGTGTGTGTAT[C/T]TGTGTGTATATGCAT | 51429 |
| rs151289835 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157878138 | AGATTCTTACTGAGT[A/T]GTCTCAGGTGAGCAG | 51429 |
| rs151299000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157848848 | TAACCGATTTTGCAC[A/G]TCATAAAATGCTTCC | 51429 |
| rs151302451 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157740611 | GTGTCCAGCATTGGC[C/G/T]GGAGAGCTCTGCAGA | 51429 |
| rs151306605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157837896 | GAACAGCATATGCTG[C/T]ACCATTAATTATGGA | 51429 |
| rs180799594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157757949 | GAAGACTAAGAAGCA[A/G]ATGGGGAGGCCAGGA | 51429 |
| rs180802704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157739270 | AAAACAAAAAACCCC[A/G]TCAAAAAGTGGGCAA | 51429 |
| rs180805730 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157715453 | GGGAGGCTGAGGTGG[A/G]AGGATTGCTTGAGCT | 51429 |
| rs180809166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157726056 | ACACACTCCCTCTCA[C/T]GAGGAGTGGCCAGCA | 51429 |
| rs180809873 | snp | A/T | 0.0244538 | 0.107838 | intron-variant | SNX9 | GRCh38.p7 | 6:157750138 | CAACAATAGAAAAAA[A/T]TTTTTAAATTCATAT | 51429 |
| rs180834217 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157797990 | TTGGTATTTGGCAAC[C/T]TAGTAATTATTAATG | 51429 |
| rs180842923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157767706 | GTACCACAATCTCAG[C/T]TCATATGAAGATCCT | 51429 |
| rs180845813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157807355 | ATTTGATCATGTTTC[C/T]CTGTCACTTAAAATA | 51429 |
| rs180846859 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821746 | AAACAGTCCTGTTAA[C/T]AAACACATAGGTTGC | 51429 |
| rs180852593 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157861105 | TCTTGAAAATTTTAC[A/G]TACAGAATATTTAAA | 51429 |
| rs180855093 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157828427 | TGTTTCTTTTCTGGA[A/G]TGCTGTTCTCCCTTG | 51429 |
| rs180855198 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157777182 | GGATCACGAGGTCAG[C/G]AGATCAAGACCACGG | 51429 |
| rs180863950 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157900638 | TAGGGTCATTTGATT[A/G]TGAGGTGAGATGGTC | 51429 |
| rs180885326 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157933539 | CCTTACCATGTCTTA[C/G]AGTTGACACTTTTAG | 51429 |
| rs180889725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157942203 | ACTAAAATTTGTGTA[C/T]GTGTTCATGGAGCAG | 51429 |
| rs180894046 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157839509 | TTACTTACTGCTTCA[C/G]TTTCCTTATCTGTAA | 51429 |
| rs180909943 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157880055 | AGCCCTTCTGGCCTC[G/T]GTCACATGCTCTCCC | 51429 |
| rs180910046 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157916062 | TTGTTTGAGACGGAG[A/T]CTCGCTCTGTCGCCC | 51429 |
| rs181064049 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157855819 | TCGGCTCACTGCAAC[C/G]TCCACCTCCTGAGTT | 51429 |
| rs181065107 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157745545 | TCTGTAATTTGCGGA[G/T]CCAAGAAAAGAAGAC | 51429 |
| rs181073905 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157720066 | AAGTGAAAAAAAAAA[C/G]AGTCAAGACTTGAGC | 51429 |
| rs181077991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157833783 | CAAGAGTTGAATAAT[A/G]TGATTTTACAGTTGT | 51429 |
| rs181079553 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157876187 | GGCACAGTGGCTCAC[A/G]CCTGTAATCCCACCA | 51429 |
| rs181084281 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157801782 | TGTGAGAAGAAGGTG[C/G]CTGTTGTGTCTGATG | 51429 |
| rs181089523 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157911289 | GAGGCCTGTAAGAGA[C/T]GTAAAAGAGACACTG | 51429 |
| rs181093818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157897544 | CAGAGTTTTGCTCTC[A/G]TTGCCCAGGCTGGAG | 51429 |
| rs181094400 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157760228 | TTATATAACCCTGTT[A/C]TGCTGCACATCTCTT | 51429 |
| rs181095114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157929940 | TTGGCTTGCCACTTA[C/T]TTTGTAAATAAAGTT | 51429 |
| rs181096020 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157783114 | CATAAGAAAACTGGG[G/T]TGGCTATATTACTTT | 51429 |
| rs181100847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157733640 | TACACGGCAGCTAGG[A/G]CCATGGTGAGGGACG | 51429 |
| rs181101272 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157944683 | CGTAGGTCAGTGTTG[C/T]GGTCCGGGAAGCGTA | 51429 |
| rs181101655 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157755576 | TCGATTTAACTCAGT[C/T]GGATTATACGGTGAC | 51429 |
| rs181121035 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157815669 | GCGTGAAATAAGAAG[A/C]AGCTAATACACATAT | 51429 |
| rs181129480 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157864218 | CCTGACACAGCAGAC[A/G]GGTGAGCGAGAGTAA | 51429 |
| rs181129774 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SNX9 | GRCh38.p7 | 6:157826399 | CAGCTACTCGGGAGG[C/T]TGAGGCAGGAGAATA | 51429 |
| rs181130677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157793609 | TTAATAGGATGCTAG[C/T]GAATGCTGGTCTTTT | 51429 |
| rs181133105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157772530 | CAGCCCGCTGGCAGC[A/G]CCTGAAACAGACGAG | 51429 |
| rs181138242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157843209 | GGGTTGAAGAATTGA[C/T]GAAAATGAAAATTGA | 51429 |
| rs181146914 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157884605 | CACTCCCACCCCCCC[A/G]TATGAATTCTTTTTA | 51429 |
| rs181266770 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157769620 | CCTCCCGAGGGCAGC[A/G]TGGGAGAAAGCCACA | 51429 |
| rs181270704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157751765 | TTAAATTCATAGGAA[C/T]AAAGAGCAGAATGGT | 51429 |
| rs181272800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157728058 | TGCAGCCTTGGTCGA[C/T]GGCTTGTCAAAAAAT | 51429 |
| rs181279936 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157828814 | AGCATCACTTCCCCG[A/G]GAAAGCCTTTCCTGA | 51429 |
| rs181284271 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157879556 | ACAACCATTTTATTA[C/T]CTTTGAAAAGAAAGC | 51429 |
| rs181293412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157789477 | GTGTTCCAATATAAC[C/T]TTATTTACAAAAAGA | 51429 |
| rs181297365 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157809069 | AAATTGAATTTGTAA[A/C]AAAAAGTCTTCCCAT | 51429 |
| rs181298688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157860596 | AAGATATCTTTGTCT[A/G]ATTGTTCTTGTGTGC | 51429 |
| rs181304929 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157850182 | GGCAGTCAGGTGGGT[G/T]GAGGGCCTAGCATGG | 51429 |
| rs181306326 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157900440 | GCAGCCCGCAATGCA[A/G]CGGGGTTCTCTTTGT | 51429 |
| rs181312893 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157933226 | TTGAGCCCAGGAGGT[C/T]GAGGCTATAGTGTGC | 51429 |
| rs181314335 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157915880 | GTTGTATTGTAAATG[G/T]TACTGTTTTTTAAAT | 51429 |
| rs181331084 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157757421 | TCAACAAACCTTCAC[A/G]GACTGCCCATCAGTT | 51429 |
| rs181337116 | snp | G/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, downstream-variant-500B | SNX9, LOC107986663 | GRCh38.p7 | 6:157714897 | AAATACAAAAAATTA[G/T]CTGGGAGTGGCAGTG | 51429 |
| rs181358663 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157797567 | GATACCCATTCACAA[A/T]GTGCACACCTAGAGT | 51429 |
| rs181390429 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157839322 | TTTCTCTTGAATTTT[A/G]TATTTAGAATAAAAG | 51429 |
| rs181423504 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157870350 | CACACTCACACTCAT[A/G]CTCTCACACATGCAG | 51429 |
| rs181432075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157907492 | GGTTTCACCATATTG[A/G]CCAGGCTGGTCTTGA | 51429 |
| rs181440009 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157941720 | TACTGGTGGCATCTG[C/T]GAGCTGGACACTGCT | 51429 |
| rs181455989 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157738963 | TCAAGATGGATTAAA[G/T]ACTTAAACATAAGAC | 51429 |
| rs181473248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157820182 | GGTGCAGTGGCTCAC[A/G]ACTGTAATCCCAGCA | 51429 |
| rs181481108 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157755059 | TCATGGTGCAGGTGG[A/G]AGTGTAGCAGTGAGG | 51429 |
| rs181481610 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157776845 | ATTAGAATCTCAGGT[A/T]TGATATTTACGGGCT | 51429 |
| rs181484790 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157772213 | GGAGAGGACAGGGAT[A/G]GGTCAAGGATTTCTG | 51429 |
| rs181497290 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157732942 | CTGCTGTTTGACTTT[G/T]TCAGATTCTACATTT | 51429 |
| rs181502144 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157814244 | TAATTTTTAATGGTT[C/T]CCCATGGCCTCCCAA | 51429 |
| rs181513368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157833638 | ACATTGGTAATTTTA[C/T]CTGCCACCATGTGCC | 51429 |
| rs181515242 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157792733 | GCCTCCCACCTCTCC[C/T]CCAGCCCCTGGTCCT | 51429 |
| rs181543943 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157891151 | ATTCTCCTGCTTCAG[C/T]CTCCCAAGTAGCTGG | 51429 |
| rs181576611 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157926641 | ACAAAAATTAGCCAG[A/G]CATGGTGGCATGCGC | 51429 |
| rs181616821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885987 | TTACCATTTTCATTA[A/G]TTCTTAAACCTAGCC | 51429 |
| rs181618691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157921978 | AGGCCCCAAACTCTG[A/G]AGGTATTATCAGCAT | 51429 |
| rs181631365 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157937950 | TGTACAACTTCAGAT[A/C]ACTTAATATAAAACT | 51429 |
| rs181686410 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157727591 | TGCCTCAGTTACCTT[A/G]ACTCATCTCAGACTT | 51429 |
| rs181694622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157784898 | CATTTAAGGAACATA[C/T]TAAACATTTAAGGAA | 51429 |
| rs181705087 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157826945 | TATATAATATATAAA[A/C]TATATTATAGTTTAT | 51429 |
| rs181716574 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157896444 | AAATATAAAGCAGTT[C/G]TTTGTGAATGTGTAC | 51429 |
| rs181728089 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157865954 | TGCCTTTGAGGACAA[A/T]CAATTACTTTTAAAC | 51429 |
| rs181741123 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157929115 | ATATAGTTAGTAGTA[A/G]AAAATATGTCACAGC | 51429 |
| rs181809604 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157839927 | TCTGTCTTAATGTGA[A/T]ACATAGCTGTTTGGA | 51429 |
| rs181815320 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | SNX9 | GRCh38.p7 | 6:157762030 | TCTGGAGTGGGGCGC[A/G]CCGCAGGGAGCACGG | 51429 |
| rs181821535 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157861709 | AGGGATGCCTGCAAC[C/T]AAGGATAATACCAAA | 51429 |
| rs181822411 | snp | C/T | | | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822274 | ATTTACATTTGATAG[C/T]TGTCTCTTCTTACAA | 51429 |
| rs181828170 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157926056 | CAAGGGGAGAAGCTC[C/T]CATGACCTAATCACT | 51429 |
| rs181828342 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157880397 | CTACCCTCTCTAATC[A/G]TGTAGATTCCCTTAT | 51429 |
| rs181832109 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157907343 | CTGGAGTGCAGTGGT[A/G]TGATCTTGGCTCACT | 51429 |
| rs181834344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157941427 | CGCCATGGAAATCGC[A/G]GAGAGAAAACCAAAA | 51429 |
| rs181840240 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157901818 | CCAGTAGGTAGTTAC[C/T]GTCAGAAAATTAAGT | 51429 |
| rs181853300 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157844352 | AGTGCTGATTGGTCA[G/T]GGGTGAAATCACAGG | 51429 |
| rs181874794 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157802866 | AAAACTCGATGAACT[G/T]GCAACACCCCTGGAC | 51429 |
| rs181880963 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | SNX9 | GRCh38.p7 | 6:157874456 | TAAAGGAATAGTGAT[A/T]ACAGATATTCTTGGG | 51429 |
| rs181881767 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157910215 | TGGAAGTTGCCTAAA[A/C]GTCTCACAAGAACGT | 51429 |
| rs181898389 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157732017 | CCTTCCTTTGGCAAG[A/G]GGGCAGGGAAGAGCC | 51429 |
| rs181920295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157768718 | AGAAAATTTTGAAAC[A/G]CACATATCATCTCAG | 51429 |
| rs181922513 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157754496 | TCTACTGGAAGGAAG[A/C]AGTTGGGTGGCTGCA | 51429 |
| rs181948170 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157849775 | AGAAGGCTGGGGAAT[A/G]CTGGAGAGAAGGCAG | 51429 |
| rs181955857 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157808121 | ATAAACAAAAACTAT[A/G]AACTGCAGGAAGAAA | 51429 |
| rs181973334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890773 | AGAGTGATTGTATAT[A/G]TCGATTTTGTTTGTT | 51429 |
| rs181979412 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157784036 | ATCAAAATGTATAGA[G/T]CATAAATGAGTAGAG | 51429 |
| rs181985591 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157802146 | AGGGAATGATTTGTT[C/T]ACTTAAGGCTGCCCC | 51429 |
| rs181990557 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157916191 | AGGCACCCGCCACCA[C/T]GCCCTGCTAATTTTT | 51429 |
| rs181998988 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157944479 | TGTAGAAGCCAACAT[A/G]TAAATAAATTGTTTA | 51429 |
| rs182000133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157843541 | CATTGAGTAGGTGGA[A/G]GAAAAGGAGGGTGGA | 51429 |
| rs182015546 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157826859 | TATTTTATATATAAA[C/T]ATATATTATAGTTTA | 51429 |
| rs182020164 | snp | G/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885496 | CTCTTCAGTCCCTTT[G/T]GAGGAAAAGAGTTAA | 51429 |
| rs182024144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157930469 | GCCCCCAATCCCCAG[A/G]CCATGGACTGGTACA | 51429 |
| rs182030556 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157865409 | TTTTGCAGCCATGTC[A/G]GGAAAACACCTCAGC | 51429 |
| rs182041174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157903395 | TTTTGACTGCACACT[C/T]TTGCTGCCTCTTACC | 51429 |
| rs182045629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157939414 | AGGCATTAAGAAGCC[A/G]TTAAAAGGGAGTAAA | 51429 |
| rs182158615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157718810 | TAGCAGAAGGAGTAG[C/T]AGGTCCCAGCCTCAG | 51429 |
| rs182178564 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157720651 | AAGGCAGGCCAAGGG[A/T]GACGCTGACCCTCTG | 51429 |
| rs182186713 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SNX9 | GRCh38.p7 | 6:157760061 | TTTTTTCAGTAGAGA[C/T]GGGGTTTCACCATGT | 51429 |
| rs182188814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157778597 | AAGAACCATTTCTTG[A/G]TCATCTACTCTGCGT | 51429 |
| rs182201494 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157788399 | CAACAGTGAACTATG[C/T]CTGCATTGGCTTGTC | 51429 |
| rs182203259 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157742701 | TCTTTTGGGCCGATG[A/G]CATTTCTCCTGTAGA | 51429 |
| rs182205359 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157824430 | GCACTTAGTTTTTGT[A/G]ATGTCACTTTGTTAG | 51429 |
| rs182207024 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157850988 | AGGCTGGGCGTGGTG[G/T]CTCATGCCTGTAATC | 51429 |
| rs182214547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157829416 | GCTAACTTTATTCCC[A/G]GCATACAGTCAGCTT | 51429 |
| rs182216966 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157750907 | TGCAAATCAAAACCA[C/T]AATGAGCTAGCACTT | 51429 |
| rs182218802 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157828793 | TATTAGGTCTTAATG[C/T]GTCTAAGCATCACTT | 51429 |
| rs182219616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157761487 | CTTGTTTTGTGTGTG[C/T]GGTCAAATAAGTCAG | 51429 |
| rs182220680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157871239 | ACAAAAATTTAGCCG[A/G]GTGTGGTAGTGCGTG | 51429 |
| rs182220859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157799964 | TTTCAAGCATCCCAC[A/G]GGCATTCATGAGGGG | 51429 |
| rs182227478 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157907646 | TACAGAGCTAAGGGT[C/T]CCAGCCTTTCATTGA | 51429 |
| rs182231844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157891577 | ACATCACATTTAAAA[C/T]ATTTGAGTCCTTGCC | 51429 |
| rs182233402 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157926688 | TTGGGGGCTGAGGTG[A/G]GAAGATTGCTTGAAC | 51429 |
| rs182242888 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157869910 | ATGCGCACACACCTC[A/G]CACCCTCATACACCT | 51429 |
| rs182293512 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157934278 | TGAGCATATGGAAAT[A/G]TAAGCAATAAAAATT | 51429 |
| rs182293832 | snp | G/T | 1.65222e-05 | 0.00287417 | intron-variant | SNX9 | GRCh38.p7 | 6:157937568 | CAACAGCAGGTGAAG[G/T]AGGCAGATGTGCGCA | 51429 |
| rs182313767 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157911977 | CTCGTGGTGCTGGGG[C/T]GGTGGAGTGACAGCC | 51429 |
| rs182367841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157723866 | TTTGACTCACAACAC[A/G]TCTGAGACCAAATAT | 51429 |
| rs182386530 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157762267 | TCACTGGGTTCGTTG[C/T]AGTTTTCAAGCGTGC | 51429 |
| rs182394789 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SNX9 | GRCh38.p7 | 6:157747082 | AGGCAGAGCTCAGGC[A/G]GTAATGCTCACTTGT | 51429 |
| rs182406861 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157826983 | ATACATATATATTAT[A/G]GTTTATATAATATAT | 51429 |
| rs182417334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157785113 | AGCCGGGTGTGGTGG[C/T]GGGTGCCTGTAATCC | 51429 |
| rs182418758 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157803755 | CTTGTATGTGAATTT[A/C]TTCTGTTTCTTTGTC | 51429 |
| rs182441644 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157771441 | AACCTCAGTTTCCCC[A/G]CACACAAATGGATGT | 51429 |
| rs182442936 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157746008 | TTAAAATCTGCTATC[C/T]CTGGAATTTTGGTTC | 51429 |
| rs182534631 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157752353 | CTCAGCATATGGAGG[A/G]TCTGCGCAGGCACCA | 51429 |
| rs182548667 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157898009 | GGTTAGGAGATCTGT[G/T]TCAGGAGCCAGGGTC | 51429 |
| rs182557054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157920920 | AACTTCCATTATTGC[A/G]TTAGTGGAAAAATTC | 51429 |
| rs182571145 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157790185 | CTGGGAGATGTAGTC[C/T]TGTTCCGAGTTTTCC | 51429 |
| rs182584585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157878281 | GCTGCAGTTTAGACT[A/G]GAATTGTCAGTGTGA | 51429 |
| rs182596604 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157858652 | GTTCTCACACTGCTA[G/T]TAAAGACATACCTGA | 51429 |
| rs182602832 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157862900 | GTTGCAAGTGACAAG[A/T]TGTGGACTGACAGTT | 51429 |
| rs182603547 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157899237 | TCCCACACCCCAACT[C/T]GGTCTTTTTAATGTC | 51429 |
| rs182613411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157931054 | CAAGGCTAAATGTAG[A/G]AAGTAGGGAATACTG | 51429 |
| rs182616718 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157913815 | CAATTCAATCATTTT[G/T]TTGTGTCAATAGTTT | 51429 |
| rs182629228 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157902425 | ACTTGCCATGTGCCA[A/G]GCATTGTGCAGAGAG | 51429 |
| rs182633985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157935939 | TGCATAACTTATAAC[C/T]ACTGATAAAATTGAT | 51429 |
| rs182789497 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SNX9 | GRCh38.p7 | 6:157769942 | ATGGCTGGCTTCACG[A/G]GCAGGTGAGCTGAGC | 51429 |
| rs182799680 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157737259 | ACCTCTGGTATAATT[C/G/T]GGCTGTGAATCCGTC | 51429 |
| rs182808726 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157728909 | GTTCAAGACCAGCCC[A/G]GCCAACATGGCGAAA | 51429 |
| rs182811227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157881981 | AAACAGATTTTCAGA[A/G]CAGATGAAACAGCCT | 51429 |
| rs182818446 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157902180 | GATATGATTCAGTTA[G/T]TTTTATTTGGATCTT | 51429 |
| rs182818652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157811999 | AGGCCTCAGAAATCT[C/T]AGTAGGATCCAAACT | 51429 |
| rs182820439 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157774132 | AGAGGCAGACGCAGC[C/T]CAGAGGGAGAGGACC | 51429 |
| rs182821290 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157852680 | ACCTCCTGTTTAAGC[A/G/T]ATCCTCCCACTTCTA | 51429 |
| rs182824815 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157831905 | GGGAGTGGAATATGT[A/G]CATGAAAGTGTTAAT | 51429 |
| rs182825497 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SNX9 | GRCh38.p7 | 6:157721531 | GATTGTCGTCTGCCC[C/T]GCTTACAATGCTACA | 51429 |
| rs182833775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157809600 | GATAAAGAACATATC[C/T]AAAACAGATTAAGAA | 51429 |
| rs182837040 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157916386 | GGAATAGAGAGTTTT[A/G]TTTCATCTTTTCCAA | 51429 |
| rs182838543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157872557 | GAGTCTGCCAGTTCT[C/T]TGGGTTGGCTGGCTT | 51429 |
| rs182846280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157935287 | CAAACTCATACTAAA[A/G]TAAAAGATCCAGACA | 51429 |
| rs182857171 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157844844 | AAATGATTTACCCAC[C/T]TTGGTCTCCCAAAGT | 51429 |
| rs182857542 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887149 | TTGAGCCTTGTTCTG[C/G]GATGCACCTAAGTTA | 51429 |
| rs182861669 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157841341 | AGGAGAGGCACAAGA[C/T]AGAAATACAGATTTT | 51429 |
| rs182866517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157818398 | TGGGTCTGCCTTCCC[C/T]AACCCAGTGACTCAA | 51429 |
| rs182876352 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157922870 | AACTAAGTTCTTTGA[A/T]TTCAGTAAATATTTG | 51429 |
| rs182894027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157882782 | ACAGATGAGGAGTTG[C/T]TTCTTATGGATGAGC | 51429 |
| rs182900433 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157918004 | ATTTTTAGTCCTCTT[A/T]CATTTATTGAGACTT | 51429 |
| rs182930600 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157905540 | AAGTGACCTCCCCCC[A/C/G]ACCCCCTCCCCATAG | 51429 |
| rs182940526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157923720 | AAGCTAAAAAAGTTT[A/G]AAAGCATGGCATTGG | 51429 |
| rs182949847 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157940124 | TGAAGAAGGGTCTCC[C/T]GCTGTCCCACACGCT | 51429 |
| rs183028554 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157795148 | AGGCGGGGCACGGTG[C/G]CTCATGCCTGTAATC | 51429 |
| rs183036190 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157756274 | AAAAATTGGCTGGGC[G/T]TGGTGGCAAGTGCCT | 51429 |
| rs183036319 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157773356 | CTGCACAGAGGCAGC[C/T]GAGGTGCAGAGGTCA | 51429 |
| rs183052057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157857207 | TGTATTCTTCCACAT[C/T]TGGACAGCAAGCTCA | 51429 |
| rs183052243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157817600 | CGTGGTGGCTCACGC[C/T]TGTAATTCCAGCATG | 51429 |
| rs183057152 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157836417 | TAAGCTTCCATCTGA[C/G]AGAGAAATTGAACTC | 51429 |
| rs183061969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157877113 | AGCTATTATCTCAAG[A/G]TAGGTGGAGGCAGTT | 51429 |
| rs183094371 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157716985 | GTCTGTCATCTCCGC[A/C]CTTGCTGGGCTGCAT | 51429 |
| rs183125584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157759512 | TCAGCATGGCCAATA[C/T]GGTGAAACCCTGTCT | 51429 |
| rs183129789 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157795523 | GTTGTTAATTTTGTT[A/G]GGTATGATGATAGCA | 51429 |
| rs183133848 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157756681 | CCATAGCTTCTAATG[C/T]AGCAAGCAGGGAATA | 51429 |
| rs183134133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157840448 | CTTTCCTTTCTTTCC[C/T]TTCCTTCCTTCCTTC | 51429 |
| rs183145495 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157798538 | GACTGTACTTCACCA[A/C]TGTTAATTTCCTGAT | 51429 |
| rs183150670 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157866825 | GTGTGTGCGTGTGTG[A/T]ATGTCTCTGTCTTCA | 51429 |
| rs183152058 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157836933 | GGTGATGCTGATGCT[G/T]CTGGTCTAGGGACCT | 51429 |
| rs183167394 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157927296 | AGCCAGTGTAGCCGC[A/G]GCCGAAACTCAAATC | 51429 |
| rs183179478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157904877 | TAGCGGCAGTCAGGT[A/G]TGATGAATAGAATCA | 51429 |
| rs183182597 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157942328 | GCCCTGGCGCAGAGA[A/C]CACTGCAGCGCCTCG | 51429 |
| rs183188385 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157918620 | TATTGACATGGTTAG[A/C]TTCACATTTGCCATT | 51429 |
| rs183192370 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157938476 | TCCAAGGGACTTGAA[A/G]GAAGTTAAATTTAGA | 51429 |
| rs183217540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157908232 | TTTCTTTTTACTTTC[C/T]TATGGTACTTTTTCA | 51429 |
| rs183229108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157753014 | CATTAAACCTTGAGT[C/T]GACACAGCCCATGTT | 51429 |
| rs183235704 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157942704 | AATTTGTGTCATGTT[G/T]AACTTGTTGGAGTTG | 51429 |
| rs183243697 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157798144 | AGAAAACCTAGAAGA[C/T]AACACTCTAATCAAG | 51429 |
| rs183249635 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157759192 | TGGCAACCTGGACGT[A/C]AGAAGTCACACGGCC | 51429 |
| rs183249987 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SNX9 | GRCh38.p7 | 6:157730250 | ATGAAGGAGCCAGGC[A/G]CGGTGGCTCATGCCT | 51429 |
| rs183266725 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | SNX9 | GRCh38.p7 | 6:157770528 | TGCGGTGGCTCACGC[C/T]TGTAATCCCAGCACT | 51429 |
| rs183371105 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157777925 | GTAAAGAGGCCCGTC[C/T]TCACCATTGTCAATG | 51429 |
| rs183387706 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157740627 | GGAGAGCTCTGCAGA[A/G]TCAGGAGCATGGACT | 51429 |
| rs183405685 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157746305 | TTTTTCCTAAAAGTT[A/G]AGGTATTCAAAGATT | 51429 |
| rs183419079 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157824011 | TGCCTTCGCTGCTGT[A/T]ATTTTTTTCTTTTGT | 51429 |
| rs183427312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157862244 | CATCAACATATGTTA[A/G]TAGCATAATAATGCT | 51429 |
| rs183427741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887821 | TTCACAGGAGAGTTG[C/T]GCCTGAAAAGGATGC | 51429 |
| rs183430783 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157846096 | TGATGAGATTGTCTT[C/T]GGCTTCTCTGCCTTC | 51429 |
| rs183433843 | snp | G/T | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157867690 | CTTATTTTTAACAAA[G/T]CCGGTAAGAGAACTG | 51429 |
| rs183437009 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157905302 | AAAGTAGAAGCAATG[A/C]GACTGGAACTTCGTA | 51429 |
| rs183443823 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB, nc-transcript-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157892958 | TTGACTGTGGCCCTC[C/T]GAGCCCCTCCATTTC | 51429 |
| rs183452010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157923394 | TGGATACAAGACATT[A/G]CATATTTATCAGCAA | 51429 |
| rs183459550 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157756045 | CAGTAATCACATCTG[A/G]TGACAGTAAATGTCA | 51429 |
| rs183464931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157735100 | AATATGGCGAAACAC[C/T]GTCTCTACTAAAAAT | 51429 |
| rs183472160 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157927360 | AGTCCAATGACAAGG[A/G]AAACATCATTTGTAC | 51429 |
| rs183480809 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157868670 | CATGTAACTTTATTG[A/T]AACTGTTCTTAAAAT | 51429 |
| rs183482366 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157898904 | CTGGGTAGAAGCGTT[A/G]GGAGACTCCTGGGGT | 51429 |
| rs183485568 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157930791 | AAGGTTGGGGACCGT[A/T]GCTCTAAAGTATAAA | 51429 |
| rs183504047 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157772963 | ATGGTGGGGAGAGAC[A/G]AGAAAGCAGACGACG | 51429 |
| rs183607314 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157869517 | CAAGGCTAAGTCACT[G/T]AAAGCCATTGGTTTC | 51429 |
| rs183614936 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157906962 | GATGAGGAAACATCT[A/G]GTCTTATTCTGTAGT | 51429 |
| rs183620360 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890592 | TTACATAGATTTAAG[C/T]GTGTCCCAGAGACCC | 51429 |
| rs183626870 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157736347 | GAGCAGTGGTGTGTA[A/G]TTCTCCTTGAAGAGG | 51429 |
| rs183637048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157925667 | AGATTTTGACTGTAG[C/T]TCCTAAGCAAGATTG | 51429 |
| rs183642145 | snp | A/C/G | 0.030278 | 0.119257 | intron-variant | SNX9 | GRCh38.p7 | 6:157739762 | ACCATGGAATACCAT[A/C/G]CAGCCATAAAAAAGG | 51429 |
| rs183644718 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157940666 | CAGGTGATCCACCCA[C/T]CTCACCTCCCAGAGT | 51429 |
| rs183697838 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157810423 | ATGAATTAAACACTT[A/C]AAATCACTGAATTGT | 51429 |
| rs183715578 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157912968 | AGAGATAAACCAGCT[A/G]TGTCAGAAAAATTTT | 51429 |
| rs183755935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157851939 | CGTAATGTTTTCAAG[A/G]TTCGTCTGTAATGTA | 51429 |
| rs183782036 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157892080 | GGAGTGGGAAGAGAA[A/G]GAGGATGAAGATGCT | 51429 |
| rs183824243 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157801958 | AAGCCCAGAGCATCC[A/C]CAATATTCAGTCCTC | 51429 |
| rs183831735 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157853899 | TTTCTCCTTTGTGTC[A/G]CAAGGCACAGGCAGT | 51429 |
| rs183837291 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157783412 | CCATTTTGACTTCAT[A/T]GATATTTATGAAACA | 51429 |
| rs183840787 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157843259 | CTTGAACAATGTGGG[G/T]GTTAGGAGCACCGAC | 51429 |
| rs183845441 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SNX9 | GRCh38.p7 | 6:157873919 | GAGCCAACCACCTGG[C/T]GCCCCCTGCTGGTTG | 51429 |
| rs183855590 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157826760 | ATTATAGGTTTTATA[G/T]ATATATGATATATAA | 51429 |
| rs183856857 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157909497 | CTTTAAACATAATAT[C/G]TAACAGGAACAGAAA | 51429 |
| rs183863463 | snp | A/C | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893961 | GAGTCCAGCTATAGA[A/C]CCAAATCTGATATGT | 51429 |
| rs183865032 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157927797 | AGTGGCACGATCTCC[A/G]CTCACTGCAAGCTCC | 51429 |
| rs183869726 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157716012 | TGGAAAATAGCCCCA[C/T]CCAGTCAAAGAACTA | 51429 |
| rs183876468 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157943240 | TGTCAGATAATTAAT[C/T]ACTAATTACTTTCTT | 51429 |
| rs183927327 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157790689 | ACTGCTTGTGAGCTC[A/C]GCTTTGACTCTATGA | 51429 |
| rs183941427 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157872145 | TGTTAAGATGAGAAA[C/G]TGGGACCTGCCCCTT | 51429 |
| rs183943613 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157900525 | AGCTGGGTCCGGGGG[A/G]GTCACTGCCTTCTGG | 51429 |
| rs183944532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157830784 | CTAGAAAATTCTCAG[C/T]GGTTATTCATGAAAA | 51429 |
| rs183963968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157915931 | TTGCATATAGAGATC[A/G]CTTGATTTTTGTATA | 51429 |
| rs183973814 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157933300 | CCCCATCTCAAGAAA[A/C]AAAGAAGAAAAAGCA | 51429 |
| rs183976702 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157908169 | CTCTGAGGTCTCAGC[C/T]GAAACAAATCTCTCT | 51429 |
| rs183998943 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157794402 | TAGCAGCATGAAAAC[A/G]GACTAACACAGAAGC | 51429 |
| rs184002594 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157763755 | GTAGCATGAAATGTT[A/T]TCCTGGAAAACCTTT | 51429 |
| rs184017627 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157749452 | TGGCACTGACCTCAC[A/C]TAGAGTATATGCTGA | 51429 |
| rs184025312 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | SNX9 | GRCh38.p7 | 6:157724549 | TAACTGCCTCCTTTA[A/C]TGTCTTGTACCTAAC | 51429 |
| rs184027226 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157725541 | GCTGACCTTGCTTTT[A/C]CACCCAAAAGTTGCT | 51429 |
| rs184042267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157876393 | GAGGCGGCCACTGCA[A/G]TAAGCCGAGATCGTG | 51429 |
| rs184045106 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157787229 | CCATAGGCTCTTCCT[A/G]GGTCTCAAGTCTACC | 51429 |
| rs184045375 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157835420 | TCCCCTTCTTTTTTT[C/T]TTTTTTTTTTTAAAT | 51429 |
| rs184050092 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157806945 | TTCCACTGGCCGCTG[C/T]TCGGCCCCTCCACTC | 51429 |
| rs184051769 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157766777 | CTGAAACCTGTACCC[C/T]CAATAAATCTTTGTT | 51429 |
| rs184086610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157827923 | CACATGTGTTACACA[A/G]CTTGTCTGGTTAAAT | 51429 |
| rs184088134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157848250 | AATATAAACATACCG[A/G]CTACCTAGCTTCAAT | 51429 |
| rs184098777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157914138 | TCAGTAGTAGTTCCA[C/T]ATCCCTACCTGCACT | 51429 |
| rs184159418 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157747166 | ACAGGTCTGTGGCCC[C/T]GAGACTGAGGACCCC | 51429 |
| rs184161143 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157815965 | GAACCACCATGGCAC[A/G]TGTATACCTATGTAA | 51429 |
| rs184171658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157903107 | GCTTGAAGGAGATAT[A/G]TTAGTAATTTATGAC | 51429 |
| rs184179426 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157919048 | AATCCTTATATTTCC[A/G]GTGCTGCTTATTTGT | 51429 |
| rs184191243 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157936853 | TCCCTTAAGAAGAAT[A/C]TAAGTTATTTTCTAA | 51429 |
| rs184193122 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157856166 | GATTTTATTTCATAA[A/G]GTCTCCTCTACTGCA | 51429 |
| rs184265834 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157931974 | GAGAATGTAGGAGTG[A/G]TTGTCAGTAATAATA | 51429 |
| rs184271432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157753533 | TGGTTGCCAAATCCC[A/G]AGATTAAAAACAGCC | 51429 |
| rs184275987 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157730663 | TTTTTTTTTTGGGTC[A/G]GAGTCTTGCTTTGTC | 51429 |
| rs184290927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157745368 | CGTGTTGATAAAGGC[C/T]GTGACACCAGCAGGG | 51429 |
| rs184297262 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157719654 | CAGCAGTCGCGATTA[C/G]AGGAGAGACACACAC | 51429 |
| rs184303128 | snp | C/G/T | 0.00199529 | 0.0315338 | intron-variant | SNX9 | GRCh38.p7 | 6:157770583 | ACGAGGTCAGGAGAT[C/G/T]GAGACCACCCTGGCT | 51429 |
| rs184329632 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157896118 | AGGAAGGAGGCTGCC[C/G]AGATTCATGAATCTC | 51429 |
| rs184358065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157792286 | GCTGGGACTACAGGC[A/G]CGCACCACCACACCC | 51429 |
| rs184361267 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157819748 | CATTATTTTCCTGTC[C/T]CCCCAGCTGTGTGGC | 51429 |
| rs184372823 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157754061 | TTTATTGATGGGGTG[C/G]TGCCAGCTGATCCAT | 51429 |
| rs184374506 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157775913 | GCTGCTACTGGGAAT[C/G]GAAGAGAGGATGGAA | 51429 |
| rs184378162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157832621 | CTCAGGAAGCTTACA[A/G]ATCCATGGTGGAAGG | 51429 |
| rs184379327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157796465 | GACTGGGTGGGGAGC[C/T]AGGCTGCCAGAGGAT | 51429 |
| rs184383111 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157860400 | GACAGAGCAAGATGC[A/G]GTCTCTCAAATACAA | 51429 |
| rs184393689 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157879276 | CAGGGGACTGATCAG[A/T]TGAACTATAGGCAGC | 51429 |
| rs184407337 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157915226 | CTTTAAATCAAGTAG[C/T]GTGAATCCTCCAACT | 51429 |
| rs184408687 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157900303 | CCTTTGTCCATTTTT[G/T]AATTGAGCTTTTTTT | 51429 |
| rs184412217 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157864800 | TTTGGGAGGCCGAGG[A/C/T]GGGCAGATCATGAGG | 51429 |
| rs184442193 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | SNX9 | GRCh38.p7 | 6:157903190 | TTGAAATTACTAATA[A/C]TTTTTCCCAATATTC | 51429 |
| rs184447896 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157731194 | AGACAGAGTTTCACC[A/G]TGTTGGCCAGGCTGC | 51429 |
| rs184461971 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157937185 | ATTATTTTGGGCCAC[A/G]TCAAAATAACTAATT | 51429 |
| rs184482391 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157771207 | GAGGTATGGATCATC[A/G]TCATGAATTTCTTTA | 51429 |
| rs184516617 | snp | G/T | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157812522 | GCATACAACTAGACT[G/T]CACTTCCAGCCTTGC | 51429 |
| rs184521256 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157747746 | CTAAAAAACAAAGCA[A/G]TGAAATTACTAATCC | 51429 |
| rs184523191 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157724739 | GAATTTGTCTATATA[A/G]ATGATTCCAAACTTC | 51429 |
| rs184564493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SNX9, LOC105378078 | GRCh38.p7 | 6:157884979 | CTTCTCTTAGGTCTG[C/T]CTGGAAGCAAATTAT | 51429 |
| rs184573454 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157920638 | TTGTTGATTTCTAGA[A/G]CACTCATTTGGTTGT | 51429 |
| rs184588426 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157771666 | CACGCAGGAGGAGCT[G/T]CCAGGGACATATCCA | 51429 |
| rs184596430 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157825451 | AATCCTGAACTTAAT[A/T]TTTTTCCAAAAAATC | 51429 |
| rs184600153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157754861 | AAAGTGAAAGCAAGT[A/G]TATTAAGAAAGTAAA | 51429 |
| rs184606444 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157732583 | ACACTTTAGATCAAC[A/T]CTCTTAGCAAATTTC | 51429 |
| rs184606477 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157800850 | TCACTCTGTCTCTTT[C/T]CAGTCCATTCTGTCT | 51429 |
| rs184625962 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157842239 | AGAACAGTGCCATCT[C/G]TTACTGGTTGACATT | 51429 |
| rs184626226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157792637 | TTAACTAAAGGCACC[A/G]TTTTCTACAATAGAT | 51429 |
| rs184627884 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157883154 | AGCAAAAAGGGTGCA[G/T]CTTGACTAGTGGAAG | 51429 |
| rs184634443 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157863419 | TAATGGAACAGATAC[A/G]TGAGATTGATGTCTA | 51429 |
| rs184678989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889718 | AAAGTCTCTATTAAT[A/G]TGACCTGGCTGTGCA | 51429 |
| rs184694686 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157860600 | TATCTTTGTCTAATT[G/T]TTCTTGTGTGCACCG | 51429 |
| rs184705211 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157924738 | CCGAAAGCCTTCATC[A/G]TGTAAATGACTTCCG | 51429 |
| rs184792464 | snp | A/C | 0 | 0 | upstream-variant-2KB, nc-transcript-variant | SNX9, LOC107986663 | GRCh38.p7 | 6:157714090 | CTCATTCTCTAGCCC[A/C]GCCATTTACCCCTAT | 51429 |
| rs184806266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157869239 | GTCATTCCACCTTCA[A/G]CCCATTTCTTTACAC | 51429 |
| rs184818708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157774534 | GGCCCTGCGGTCATC[A/G]ACCCACGTGTCTGCC | 51429 |
| rs184825451 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157756820 | TCTGATTCCGGCCAG[A/C]AGAGGGCAGGAGCGA | 51429 |
| rs184826529 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157737606 | TTCAAAAAACCGGCT[C/T]CTGAGTTCATTGATT | 51429 |
| rs184831738 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157839495 | ATTACTTTGAAAAGT[A/T]ACTTACTGCTTCACT | 51429 |
| rs184834974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157906433 | ATCTTTCAGACTTTT[A/G]GTATTGAACAAATAT | 51429 |
| rs184845935 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157795750 | TTTACACATAAACTT[C/G]TTATAAACTTTCATA | 51429 |
| rs184846325 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157940206 | CGGGGCAGGGACCCC[A/C]GCTGCCTGCTAGGTC | 51429 |
| rs184889944 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157944068 | AGCGCTTCACTTAAC[A/G]GCATAAAGCAAAACA | 51429 |
| rs184907080 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157760161 | CAGGCGTGAGCCACC[A/G]CGCCCGGGCCATCAA | 51429 |
| rs184910368 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157851207 | AGGCTACAGTGAGCC[A/G]AGATCAAGCCTCTGC | 51429 |
| rs184922615 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157871381 | ATGAGACAGTGTCTC[A/T]AAAAAAAGAAAATCA | 51429 |
| rs184932340 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157801572 | TGTCTCTACAAAAAA[C/T]ACAAAAATTAGCTAG | 51429 |
| rs184934170 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157907723 | TCTGCCTGTGTGGGC[A/G]TCTATACATGGAAGA | 51429 |
| rs184942376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157891638 | GGGGGAAACATTCTC[C/T]GGGTAAGACAGAGCT | 51429 |
| rs184946416 | snp | C/T | 0.000280521 | 0.0118398 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157927197 | ACCAGAGGCACCTGA[C/T]TTGGACTTAGTAGAA | 51429 |
| rs184958815 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157942262 | AGCCCTCGTGCTGGA[C/T]GTTTAGCATCCAGGG | 51429 |
| rs184970423 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157842771 | AATATCTTAATCACT[C/G]ATCTTAGGTTTTACA | 51429 |
| rs184984018 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157883845 | TAGCACAATTTGTGA[C/T]TCTTATACAAATTAT | 51429 |
| rs184999386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157911069 | GGTGAGCCGAGATTG[C/T]GCCACCGCACTCCAG | 51429 |
| rs185056524 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157782983 | CCAGTAGACTTAAAC[C/T]ATATCAGACAAGCAA | 51429 |
| rs185074045 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157825868 | TGTTTTTTCTTTGTC[G/T]TCTTCAAGGGGTGGG | 51429 |
| rs185077732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157863977 | TCTTAATTCAGTGTT[C/T]TAGATAAACTTACAA | 51429 |
| rs185105801 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157849198 | CGGAGGTGTTCAGGG[C/T]CAGGTGATCATATAA | 51429 |
| rs185112146 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157828493 | TTTTATGATTATGAT[G/T]ATTATTATTTTTTTT | 51429 |
| rs185131740 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157929354 | GGCTAATGCCACGGG[C/T]TGCTGCCCTGTTACA | 51429 |
| rs185149057 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | SNX9, LOC107986663 | GRCh38.p7 | 6:157714299 | AAATGCAATACCTCA[C/T]TGACTTGTATTATCT | 51429 |
| rs185167321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157876197 | CTCACGCCTGTAATC[C/T]CACCAGCACTTTGGG | 51429 |
| rs185181707 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SNX9 | GRCh38.p7 | 6:157757270 | AGCCCCATACTCTTT[A/G]TATGAGGTATGGGGT | 51429 |
| rs185183401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157897812 | TGAGCCACCATGCCT[A/G]GCCGGCATGATTGAT | 51429 |
| rs185188975 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157930000 | TGTATATTGTCTTTG[A/G]CTACATTTGTGTCAT | 51429 |
| rs185190238 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157786521 | GATAACAGATCGTAT[A/C]TATAGAAAATCCTAA | 51429 |
| rs185190568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157911661 | TCGAATCTGATCCCA[C/T]AGCTTACTCTGTTTC | 51429 |
| rs185206063 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157944684 | GTAGGTCAGTGTTGC[A/G]GTCCGGGAAGCGTAT | 51429 |
| rs185210471 | snp | A/T | 0.482008 | 0.0931261 | intron-variant | SNX9 | GRCh38.p7 | 6:157827491 | ATATAATATATAAAC[A/T]TATAGTTTATATAAT | 51429 |
| rs185267280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157932722 | AAAATAAAAAATTAG[C/T]CACGTGTGGTGGTGC | 51429 |
| rs185300000 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SNX9 | GRCh38.p7 | 6:157738169 | CCACTTGGTCCAGAG[C/T]TGAGTTCAAGTCCTG | 51429 |
| rs185302076 | snp | G/T | 0.021333 | 0.101051 | intron-variant | SNX9 | GRCh38.p7 | 6:157765457 | GCCTCCCAGGTTCAC[G/T]CCATTCTCCTGCCTC | 51429 |
| rs185310849 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157847620 | CCTTGCTGGGAAGGA[A/G]CCAGGCTATGTATAT | 51429 |
| rs185313243 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157745733 | AATGAGCCCAAGGAC[A/G]AGAATATGAAAGATT | 51429 |
| rs185328978 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157720452 | TTGTATCTCACAGGG[G/T]TCTACAGTGATGGGT | 51429 |
| rs185352749 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157760286 | CTGACAGCTGGAAAT[G/T]GGCCATGGGGGCAGT | 51429 |
| rs185377275 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157769834 | GCAGTGCTTGGAAAT[C/T]GATGACAAATGCAGG | 51429 |
| rs185385546 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157752027 | GAAACCTCGTCTCTA[C/G]TAAAAACACAAAAAT | 51429 |
| rs185395931 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157809227 | CAGACCTCATATCAA[C/T]GCTCAACAAAGTTGT | 51429 |
| rs185400375 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157828917 | GCTGGCTCCTTTGAA[A/T]GCTGTCAGCCTCAAG | 51429 |
| rs185406727 | snp | C/G/T | 0.00239393 | 0.0345281 | intron-variant | SNX9 | GRCh38.p7 | 6:157789527 | CCATCCCGCTGTAGA[C/G/T]GGCAAACTCTACTGT | 51429 |
| rs185423535 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157743496 | TAATCAAAACAACAA[C/G]AGATAAACAGAAAAC | 51429 |
| rs185428695 | snp | C/T | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157850450 | GACAGGTGGGTTAAA[C/T]ACTAATGGGAAGGAG | 51429 |
| rs185445361 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157870421 | ACCTGCTCTCACACA[C/T]GCACACTCACATGCT | 51429 |
| rs185448418 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157780510 | ATTCTCTCCTTTTCA[C/G]CAGCACTGAATGGAT | 51429 |
| rs185481696 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157813857 | CTTACTGTGCCAGCT[A/G]AAACTGGCCTGTTTG | 51429 |
| rs185492880 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157854781 | AGATTCTGTTTGCCA[G/T]CTAATCTGCTTTTTA | 51429 |
| rs185496613 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157895005 | TTTTATGCCTCACAG[G/T]GCCTGTATCACACTA | 51429 |
| rs185526171 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157928773 | TTATGTCCCTTATCA[A/T]AGAGGGGAACCTGCT | 51429 |
| rs185549971 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157760151 | GCTGGGATTACAGGC[A/G]TGAGCCACCACGCCC | 51429 |
| rs185557907 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157718958 | CAGTGCCACTGGGGA[A/C]TTCCCTTGGCCATTG | 51429 |
| rs185594831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157833165 | CTTGAAAATTTAGAC[A/G]TATGTATAAATAGTT | 51429 |
| rs185605481 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, downstream-variant-500B | SNX9, LOC107986663 | GRCh38.p7 | 6:157715093 | TCTATCTACCAGAAG[A/G]ACACAGAGTCCCATA | 51429 |
| rs185614437 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157874158 | CGTCCTTCTGTTGTT[C/G]ATAGACAGTGAGGGT | 51429 |
| rs185629379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157772254 | GGCAGTGGGACTCCC[A/G]GCAGGTAGGACTGTG | 51429 |
| rs185645777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157815117 | CACAGGTGTTTCTCT[C/T]TTCTCCCAGTGGTTC | 51429 |
| rs185646992 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157910061 | ACCCAGGATGACAAA[C/T]AGAAAGACTCCAGTC | 51429 |
| rs185649833 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157762178 | AGTAGGTCTAGAAGC[C/T]GCTCTGGGGGCAGTG | 51429 |
| rs185656460 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157833727 | TTCCAGCACTGCACT[G/T]CTCCTCCCGCCTTCC | 51429 |
| rs185666873 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157793251 | CCACGCACCCAGCCT[G/T]AGAATTACTTTTGAT | 51429 |
| rs185666946 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157746492 | GCAGAAGACTTCTTT[C/T]TGTCCTTAAACATTA | 51429 |
| rs185673195 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157855201 | ACATATATATTAGAG[A/G]TCATTCCACACCAGA | 51429 |
| rs185688509 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157875608 | CTAGAGGCCCTCATC[C/G]TGCGAGTAGAAGCAG | 51429 |
| rs185688699 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157726508 | ATGCTTCTTTGAATA[A/C]CTGGTAATTTTTTAT | 51429 |
| rs185703172 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157896536 | TACTTCTGGAGAGAA[A/G]GAAAGAGAGGGCTGT | 51429 |
| rs185712419 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157838056 | GACAGAACCTCACCC[A/T]GTTGCCCAGGCTGGA | 51429 |
| rs185719470 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157935320 | GGTCATTCTAGGTAA[C/T]GATCATTTTCTAACA | 51429 |
| rs185722759 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157767907 | CGGAGGGTGCAATGG[A/G]GAGGTGCAGGGCATG | 51429 |
| rs185746977 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157807605 | AATTTATAACTTGAG[A/G]TCTCAGATATTGGGA | 51429 |
| rs185753689 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157878949 | AGGTACTAATAGTTA[A/C]TATACTTGGGAAAAT | 51429 |
| rs185757997 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157810169 | ACAACTGCATGAATG[A/C]ATTTTTTTAAATATC | 51429 |
| rs185779191 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157839574 | CCATTGCACAGTCCA[A/T]GTGGGGGAAAAATTA | 51429 |
| rs185787427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157880203 | GAATTGTGGCTTTGG[C/T]ATAAGACCTGCCTCC | 51429 |
| rs185793085 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157916096 | CTGGAGTGCAGTGGC[A/G]CTATCTCGGCTTACT | 51429 |
| rs185837978 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157819024 | CTGTGTCTCCCAGAC[A/G]ATGGAGAAAGAAATG | 51429 |
| rs185846620 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157788005 | CAGAGCTAATATTAT[A/C]GAATGCTTATTATCC | 51429 |
| rs185856963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157750377 | GCCAAGAATCCACAA[C/T]GGAGAAAGGATAGTC | 51429 |
| rs185867769 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157859270 | TGACCAATTTAAAAT[G/T]AATTTCTTGTTTTAT | 51429 |
| rs185872701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157727734 | GATGTCTGGGCATCA[A/G]TTTCCCTGGGTTTAA | 51429 |
| rs185878653 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157899646 | GGGTGTGGTGGCAGG[C/T]GCCTGTAGTCCCAGC | 51429 |
| rs185893519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157768787 | GCTCAAGCCTGTAAT[C/T]CCAGCACTTTGGGAG | 51429 |
| rs185903544 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157861118 | ACATACAGAATATTT[A/T]AAAATTTTTATTCAT | 51429 |
| rs185906026 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157751258 | AACCCATCAGATCTC[A/G]TGAGACTTATTCACT | 51429 |
| rs185924664 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157830337 | TTCTAGGTTGACAGC[A/G]TTTTCTCCTAGTACA | 51429 |
| rs185930302 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157901269 | AATAGTTTCAGGGGG[C/T]CTCCCTACACCAGCC | 51429 |
| rs185936316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157933768 | ATGCTGGAATTTTGG[C/T]CATCATGATGGCCCG | 51429 |
| rs185949758 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157922042 | ATCACGTTGCCCTTA[A/C]AATGTAACAGCATGA | 51429 |
| rs185961699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157938327 | GCCTGATTTCCATTA[C/T]GTGCTACTCCTCAAA | 51429 |
| rs185981067 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157755798 | AAGGCAGAAGTGGAG[A/G]ACTACCCATTGGATG | 51429 |
| rs186025541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157793877 | TAAATGACCACATGG[C/T]TCCAAGGGGTCTGCT | 51429 |
| rs186045324 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157834270 | CCTCCTGGGCTCCAG[C/T]GATCCTCTCACCTCA | 51429 |
| rs186089922 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157904911 | AATATGCTCAAAATG[A/C]CTAGGAAGACTCTAC | 51429 |
| rs186128648 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157734029 | ATGGTGATGATCATC[A/G]TAATGTAAAAGATAG | 51429 |
| rs186141716 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157815715 | ATGCAGCCATAAAAA[C/T]GGATGAGTTCATGTC | 51429 |
| rs186151282 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157798186 | AATATCATCTGTAAT[G/T]AAATAAATGGAAATT | 51429 |
| rs186151753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157772633 | GCCTTCAGAACTGGG[A/G]GAGAATACATTTCTG | 51429 |
| rs186171722 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157839976 | TTGTTTCATGGTTTC[A/T]CTAGGGTTCTGAAAG | 51429 |
| rs186179843 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157861985 | GGCAGTGTCTATGGT[A/G]TAGAGATGCTGGACA | 51429 |
| rs186186841 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | SNX9 | GRCh38.p7 | 6:157823248 | GAGCGTGCGGCGCGG[C/G]AGTAGCCGAGCGCCC | 51429 |
| rs186195413 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157880604 | TTACTTCTTTCTGTG[A/C]CCTCTTTTTATTCTG | 51429 |
| rs186201544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887403 | GGGTAGACCCCTCAC[A/G]TGATGGGCTGATCAG | 51429 |
| rs186212763 | snp | A/G | 3.29527e-05 | 0.00405898 | missense | SNX9 | GRCh38.p7 | 6:157901961 | CCTCTTCCTACTTTA[A/G]GGATTCAGAGTCAGC | 51429 |
| rs186214536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157941477 | TTTATTCACAAAACA[A/G]TAACGAAAACTTAAA | 51429 |
| rs186221033 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157916192 | GGCACCCGCCACCAC[A/G]CCCTGCTAATTTTTT | 51429 |
| rs186225165 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157934894 | CAATCGTAAGGTCCA[C/T]GTCCCACCACAGTGA | 51429 |
| rs186228017 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157922915 | TACAGAAACTACAGG[A/C/G]AACCACCTCCAAGTT | 51429 |
| rs186235136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157739015 | AAGAAAACCTAGGTA[A/G]TACCATTCAGTACAG | 51429 |
| rs186266070 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157821018 | ATTTGTTTTTCACAG[C/T]CTTGCTCTTTTTAAA | 51429 |
| rs186266270 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157777102 | TGACCTTTAAAGGAG[A/G]CAAAAGCAGCCGGGT | 51429 |
| rs186317005 | snp | A/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157891202 | ACACCCGGCTTTTTG[A/T]ATTTTTAATAGAGAT | 51429 |
| rs186344518 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157926654 | AGGCATGGTGGCATG[C/T]GCCTAAAGTCCCAGC | 51429 |
| rs186363143 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157756097 | TTTATTTCATTAATA[C/T]CATCCTCAGTGGTTT | 51429 |
| rs186380504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157794570 | GAGACTGCTAAAAAC[A/G]AACACACAACATCTT | 51429 |
| rs186383699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157843828 | CAATTTCAAAGCATC[A/G]TGAGTACAGAATTCT | 51429 |
| rs186397319 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157826898 | ATAAATATATATTAT[A/G]GTTTATATAATATAT | 51429 |
| rs186398660 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157757832 | GCTAGGGCTGGCGTC[A/G]GGTGGAGGGATTCTG | 51429 |
| rs186399087 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157773056 | GATGTCGTCACTAAG[G/T]CAATTCCAGCTGAGA | 51429 |
| rs186400218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885840 | TGACCTGAAGTGGAC[A/G]TTTGGTGTCTGCTGG | 51429 |
| rs186407759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157865463 | GCCCTGAGGGGAGCC[A/G]TCCTGCTGGCCTGGG | 51429 |
| rs186412561 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157815975 | GGCACGTGTATACCT[A/G]TGTAACAAACCTGCA | 51429 |
| rs186412684 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157903509 | TTGTTTCAGAGTCAA[A/T]TTTGAAGTTTTCAGT | 51429 |
| rs186419367 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157797795 | TGGACAAATCCAGGA[A/C]AACTTGGCATCAAAA | 51429 |
| rs186424887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157937732 | TTTTAAAAATCTGTA[C/T]ATCACCTCAGGCATG | 51429 |
| rs186427737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157920935 | ATTAGTGGAAAAATT[C/T]CTTTGGTATTTCAGT | 51429 |
| rs186433388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157728124 | GGTGCAAGCTGGGAT[A/G]AAGAGATGTTCCATT | 51429 |
| rs186459405 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SNX9 | GRCh38.p7 | 6:157760078 | GGGTTTCACCATGTT[A/G]GCCAGGATGGTCTCA | 51429 |
| rs186466342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157779402 | GACGCTGTTGGTGGC[C/T]GTCTTGAAGCATGGA | 51429 |
| rs186471113 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157742784 | TGTGATTATTACATA[C/T]GTAATGTACACATTA | 51429 |
| rs186485760 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157824526 | TATTTTTTATTTTTC[C/G]ATAGGTGTTTGCTTT | 51429 |
| rs186516231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157800450 | TGAGACCAATCTGGG[C/T]AACACGGCAAAACTG | 51429 |
| rs186517288 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157733046 | TGTGTTGCTGAAAAT[G/T]GCAGGCACAGCTCCA | 51429 |
| rs186518081 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157907506 | GGCCAGGCTGGTCTT[A/G]AACTCCTGACCTTGT | 51429 |
| rs186541870 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157841794 | AACATAAAATGATAA[G/T]AATTTACTACACTGT | 51429 |
| rs186544394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157941804 | CCTAATGCATATTTG[C/T]GAATTGTGTCTTGGA | 51429 |
| rs186545145 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157844362 | GGTCAGGGGTGAAAT[C/T]ACAGGGAGTCAAAGC | 51429 |
| rs186548442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157802996 | TCCCTGGTCCCTGAA[C/T]CAGCACAGTAATGGA | 51429 |
| rs186563371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157739462 | AACAGATGCTGGAGA[A/G]GATATGGAGAAATAG | 51429 |
| rs186564707 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157715662 | ATTCTCTTTTATAAA[G/T]ATTTGGGATACGTGG | 51429 |
| rs186585020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886535 | GGTATACACACAAAC[A/G]TACAGATATAAATTG | 51429 |
| rs186585870 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157798042 | TAATAAAACTAGTGG[G/T]TGAACATTTAATGAG | 51429 |
| rs186592398 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157758144 | CTGCTGCACTCCAGC[A/C]TCCAAGGTCTTCAGA | 51429 |
| rs186688726 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157927967 | CATAACCCTTCAACC[A/G]CGCAGAGAGAAAATC | 51429 |
| rs186697044 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157762601 | AGCTTAGACAGTATC[G/T]TCAACAAAGAACAGC | 51429 |
| rs186700738 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SNX9 | GRCh38.p7 | 6:157737302 | TTTTTTTTGGTTGGT[A/G]GGCTATTAATTACTG | 51429 |
| rs186701810 | snp | C/G | 0.000399281 | 0.0141238 | missense | SNX9 | GRCh38.p7 | 6:157909668 | ACATTGGCATAGGTT[C/G]GAGATTATGGCCCAA | 51429 |
| rs186706045 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157943715 | CGGAGGCCTGTGTTC[A/G]GGAGGGCCTGGGAGA | 51429 |
| rs186712837 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SNX9 | GRCh38.p7 | 6:157747099 | TAATGCTCACTTGTC[C/T]GCCGCTCACCTCCTG | 51429 |
| rs186722544 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157755151 | TGCAACCTGCTTTAT[C/G]AGCAAGGTCTTTATG | 51429 |
| rs186724892 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157827000 | TTTATATAATATATA[A/C]ATATATATTATAGTT | 51429 |
| rs186735238 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157785635 | TAGAACTGATAAAGA[G/T]ATCTATTGAAAACCT | 51429 |
| rs186739640 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157804292 | CTTGTTTATGGTTTT[A/T]ATGTCCTGGTTTTAC | 51429 |
| rs186742266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157866877 | CAGAATGAACAGTTT[A/G]TGTATTTCCACTTCT | 51429 |
| rs186746551 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SNX9 | GRCh38.p7 | 6:157785013 | ACACTTTGGGAGGCC[A/G]AGGCGGGCAGATCAC | 51429 |
| rs186755642 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157845006 | AAGCAAGATGGAGTC[A/T]ATTAAGTTAGATCTC | 51429 |
| rs186771435 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | SNX9 | GRCh38.p7 | 6:157826954 | TATAAAATATATTAT[A/G]GTTTATATAATATAT | 51429 |
| rs186789980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157788872 | AATTTACTTACTTCT[C/T]TGGGTCTCAATTTCC | 51429 |
| rs186790104 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157716248 | AAGGTGGCTAAGGCT[G/T]CCTCCAACCCAGACA | 51429 |
| rs186797233 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157866138 | TTTTTACCACGGTGA[G/T]TCTCTCTTGGGATAC | 51429 |
| rs186806783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157828794 | ATTAGGTCTTAATGC[A/G]TCTAAGCATCACTTC | 51429 |
| rs186814699 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157759301 | GCCTGAGAGCCAAAC[C/T]AGGCTGTGACATGCT | 51429 |
| rs186816841 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157904757 | AAAAGTGTTGCAGGT[G/T]AGCCTAATTCATTAA | 51429 |
| rs186843113 | snp | A/G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157869958 | TTTACATACTCTTTC[A/G/T]CGTGTGCACTCTTAC | 51429 |
| rs186879786 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157907477 | TTATAGTAGAGACGG[C/G]GTTTCACCATATTGG | 51429 |
| rs186922436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157717650 | TACGCACAGGAAGTG[C/T]TCCATAAATGTTTTC | 51429 |
| rs186927786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157899372 | TTCTGCTTATTTGTA[A/G]ATGTATAAGACTAGA | 51429 |
| rs186944326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157931289 | GAGCTCGTGTAATTT[A/G]GATTCATGTTTCCTG | 51429 |
| rs186947819 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157913971 | TGCATACAGGTTTTT[G/T]TATGAATGTAAGTTT | 51429 |
| rs186958442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157740846 | CAGGCCTTCCAATTA[A/G]ATGGGCCTGGAATCC | 51429 |
| rs186998008 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SNX9 | GRCh38.p7 | 6:157740323 | AGAACAACTTGGACC[A/G]CTCTTGACAAGGAAG | 51429 |
| rs187022508 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157777832 | GCTAAGTGGTGCTCC[A/G]TATGCAGCTGCTCTC | 51429 |
| rs187037271 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157808850 | AAACATCAGAGAATA[C/T]ACATGTCAACAGTAA | 51429 |
| rs187052603 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157849950 | AAAGATGGCAGGTGA[C/T]GTTGTCAGAGTGGAT | 51429 |
| rs187062639 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890840 | AGAGTTAAACGAATT[A/T]CATAGTGAATAATCA | 51429 |
| rs187065083 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157746053 | ACACAAAAAGACAAA[A/T]ATAGCATCCAAAACA | 51429 |
| rs187074762 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157926357 | ATATTTTTGATTTGG[A/G]TACTCTGTGTGTGTA | 51429 |
| rs187098259 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157784139 | CTTTAAAAAAAAATG[A/C]GCAATATAAACCCAA | 51429 |
| rs187122959 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157791796 | AGCTTGGATTCATTA[A/C]CTCATCAACAAGTTA | 51429 |
| rs187129609 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SNX9 | GRCh38.p7 | 6:157770702 | GCTACTTGGGAGGCT[A/G]AGGCAGGAGAATGGC | 51429 |
| rs187143595 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157812051 | ACCTCAGTTCCTTGG[C/T]CATGGACCTCCTCCA | 51429 |
| rs187158871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157856238 | TTTTATGGTTTTTTA[A/G]AAAGACATTTTATTG | 51429 |
| rs187167109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157898349 | ATGGGCGGTGGAGGC[C/T]GCAGAAGGCTGAGGG | 51429 |
| rs187170762 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157852705 | CTTCTACCTGCCAAG[C/T]AGCTAGGACTACAGA | 51429 |
| rs187176726 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157831960 | AAAAAGTTGTTAAGC[A/G]TTTTGGTTGAAACCA | 51429 |
| rs187181611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157872613 | TCTCTGTCATCATCT[A/G]GCAACCCACATTAAT | 51429 |
| rs187184691 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157916606 | AGGAATTTCTCTTCT[A/G]TTTCTAGGTTGTTGA | 51429 |
| rs187186194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157909153 | CTACTCAAAGTATGG[C/T]CCACAGACCACTTGC | 51429 |
| rs187192875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, nc-transcript-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157893123 | TATATTGCTAAATAG[A/G]AGAATAAAACTACAT | 51429 |
| rs187262035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157720740 | TACCCAGCTGACTGT[A/G]AAGCTGCCCTGCCTG | 51429 |
| rs187289322 | snp | A/C | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157761549 | GTCTAGCATTGTACC[A/C]TGCACAGCAAAAAGG | 51429 |
| rs187294318 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157940136 | TCCCGCTGTCCCACA[C/T]GCTGCCCAGCCTTTC | 51429 |
| rs187330158 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157802843 | GTAGAATACCTGTGA[A/C/G]TGTACACAAAACTCG | 51429 |
| rs187349032 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157748112 | GTTAAATACAAAACA[A/G]CATCATCCATCATAT | 51429 |
| rs187361391 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157835573 | GGCTTCGTGTCCCCA[C/G]CCAAATCTCATCTTG | 51429 |
| rs187366151 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157795372 | AGTGAGCCAAGATTG[C/T]GCCACTGCACTCCAG | 51429 |
| rs187370217 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157724930 | GGATTTTGGTATCCT[C/T]AGGGGTCCTGAAACC | 51429 |
| rs187373597 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157876757 | CTGAGCCTCATTGCC[C/G]TTTGAGGCCCCGCGC | 51429 |
| rs187375688 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157836806 | CCATGTTAGCCCGGA[C/T]GGTCTCGATCTCCTG | 51429 |
| rs187376630 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157912008 | AGATGGCCGTGGGCT[A/G]CTGCTGCCTTCTGCC | 51429 |
| rs187386857 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157857418 | TGAAAAATGCTGCTC[A/G]GAATTCCCAATCTGG | 51429 |
| rs187386976 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157766306 | TAGCCACTCACTGGC[A/G]CTTCCCCTGGAATAT | 51429 |
| rs187386996 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157818145 | TTTTTTAAGTATTAA[C/T]ACACATGATCACAAG | 51429 |
| rs187390233 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157945469 | GGGGCCATGAGACTC[A/G]TGGGTCTACTCACAT | 51429 |
| rs187390377 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157786849 | AGAGGTGCTAGAACT[A/G]TCTCCACTTGCTTTA | 51429 |
| rs187398886 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157877381 | GCAGAAAGCATAGCC[A/G]TCATTAATTTGAGCA | 51429 |
| rs187405506 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157913605 | TGCAACCACCACTAC[A/C]TTTCATGATACAGAA | 51429 |
| rs187406695 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157898985 | CCATTTGGCATTTGT[C/T]TCTCGGCTTCTCCAT | 51429 |
| rs187445303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157770110 | ACGTTTTCCACAGAT[C/T]TATGCAGAATTTCGC | 51429 |
| rs187474456 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157825700 | AAGAGCAACGAAGCA[A/G]TTATTAAAAGAAGAC | 51429 |
| rs187488954 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157883509 | GACGCTGAACGGTTC[A/G]TGGTAGGGAAACTGT | 51429 |
| rs187491656 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157842688 | TTAATGTCTTCTGTT[A/C]CTGGGTTGGATGGCA | 51429 |
| rs187493745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157863608 | TAATAGTGGAAAATG[C/T]AGTATAGGAAAATGG | 51429 |
| rs187494432 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157882918 | GCAGCAGGATTTGAG[A/T]GAATTGATTCCAGTT | 51429 |
| rs187502317 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157918201 | CAATTATTGAGTATC[A/G]GGTATTGAAATTTAA | 51429 |
| rs187519025 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157918825 | TGCACTTTAGATTAA[A/T]ATTAATTCCAGTAAA | 51429 |
| rs187554541 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SNX9 | GRCh38.p7 | 6:157753081 | AACAGCATCTCAAGG[C/T]AGAAGAATTTTTCTT | 51429 |
| rs187558931 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157730297 | GGGAGGCCGAGGCAG[A/G]TGGATCGCCTGAGGT | 51429 |
| rs187585562 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157790711 | ACTCTATGACCAGGC[C/G]TTATCTCTGCAACCA | 51429 |
| rs187592290 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157770559 | TTGGGAGGCCAAGGC[G/T]GGCAGATCACGAGGT | 51429 |
| rs187655314 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157724000 | CCCACCAGTTGGGGG[C/T]TCGGCCCTGTAAGAC | 51429 |
| rs187671397 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | SNX9 | GRCh38.p7 | 6:157756700 | AAGCAGGGAATAGAC[A/C]CTCCAGCAAGCAAGT | 51429 |
| rs187683443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157837066 | CTGCACTAGCATGCC[A/G]TGTGCAGTGAACACT | 51429 |
| rs187695012 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157795528 | TAATTTTGTTAGGTA[C/T]GATGATAGCATTATG | 51429 |
| rs187697806 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157790367 | ACTTTGAAATAGGAA[A/G]AGCACCACAAAGAAG | 51429 |
| rs187704736 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157878342 | ACTGAAACAGTTTGA[C/T]TTGGAAAATTATAAA | 51429 |
| rs187729783 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157863037 | ATTCTGTGCTACATT[C/G]ACTTCGTTTTTCAGA | 51429 |
| rs187753423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157846395 | AATTGCCCTGAAGAG[A/G]AACTGCTGATAAAAA | 51429 |
| rs187755146 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157867968 | CAACCTTTTAGGTAC[C/T]CCATAGTTGTCCTGG | 51429 |
| rs187758883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157905384 | TTACTAAAAGAAAAA[C/T]TCTAAAACCCAAATT | 51429 |
| rs187765192 | snp | C/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888047 | GACCCTAAGAGCACA[C/T]ACCGGGAGACATTGT | 51429 |
| rs187768612 | snp | A/G | 5.34269e-05 | 0.00516823 | missense | SNX9 | GRCh38.p7 | 6:157935979 | GTGAAACAGATCTCA[A/G]TGATGCAATAACAGA | 51429 |
| rs187779598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157923580 | ATTTTCTAATACTGC[A/G]TCTCATGGACTGGAA | 51429 |
| rs187783638 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157939578 | GTACTGGGGAGAAGA[G/T]AATGAAGCACATTTG | 51429 |
| rs187803787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157735162 | CCTCTAATCCCAGGT[A/G]CTGGGAAGGCTGAGG | 51429 |
| rs187915330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157778354 | ATCTGCAAATACCTT[A/G]TTTCCAAGTATCTTT | 51429 |
| rs187933355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157718876 | AACTCCTTCTTCCTC[C/T]TCTCTTTTCTCCAAT | 51429 |
| rs187942770 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157774152 | GGGAGAGGACCCAAT[A/G]GAAAGGCCAGCCAAG | 51429 |
| rs187954465 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157824033 | TTCTTTTGTTTTGCT[A/G]CCTTTTCATTGTGAA | 51429 |
| rs187962692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157862398 | GCCATTTAAAGAGGT[A/G]AACTAGTTATACATA | 51429 |
| rs187972713 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157902341 | AAGGTTTCATTGCTA[A/T]TGTCACAGGAAAGCT | 51429 |
| rs187990010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157818454 | TCACAGACACACCCA[A/G]AATCAATACTTTGCA | 51429 |
| rs188001725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157858976 | AGACACAGCCAAACC[A/G]TATCACATACTCTCC | 51429 |
| rs188016964 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157927478 | GAGTAGCTGTTTCCA[A/G]TAGTGTGATGAAACC | 51429 |
| rs188117020 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157745928 | AAGCATGGAAAGAAA[G/T]AAATTTAGAGAAAAA | 51429 |
| rs188147604 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157783531 | AATTTTGAAAGACTA[A/G]CATTTTAAAGTATGT | 51429 |
| rs188151451 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157802133 | CATAGACTAAGATAG[C/G]GAATGATTTGTTTAC | 51429 |
| rs188152624 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157736612 | CAAACAGAGACAATT[A/T]GACTTCCTGTCTTCC | 51429 |
| rs188153430 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157761137 | AGAAAAACACTGCAG[C/T]GGTCTGCTTTCTATT | 51429 |
| rs188165976 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157843292 | CCTGCCCAGTTGAAA[A/G]TTAAAGTATAACTTT | 51429 |
| rs188176193 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | SNX9 | GRCh38.p7 | 6:157865353 | AGGAAAAAAAAAAAA[A/C]AAAAAACACCACATA | 51429 |
| rs188181324 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157773656 | TTGGCTGCCGTCCAG[C/G]GAAGAGATGATCAAT | 51429 |
| rs188184809 | snp | A/C | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894089 | GTATCATTTCTTTTT[A/C]TTTTCGCTTTTCTTT | 51429 |
| rs188191431 | snp | A/T | | | intron-variant, nc-transcript-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885269 | TGGCTATAAATAGAT[A/T]GAGTCTGCTGTGATC | 51429 |
| rs188198608 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157730991 | TGTTACTTTGTCATT[A/G]TTATTATTATTATTA | 51429 |
| rs188208484 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157806579 | TAATCTTAAAATCAA[A/G]TAAAAAATGGCAGCT | 51429 |
| rs188221092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157840650 | TCTTATTAAAGCCAC[A/G]CTAGGAAAATCCTGT | 51429 |
| rs188226872 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157799241 | CCCCTGACACACGGG[A/G]ATTACAATTCGAGAT | 51429 |
| rs188251027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157847709 | CATAGGTTACACGTC[A/G]TCTATTCTGGTTTTA | 51429 |
| rs188259781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888952 | GTGTGGTACCACGGA[A/G]AGAGGGAAAAGAAGA | 51429 |
| rs188262202 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157882602 | CATGGAAGAAGGTCA[A/G]AATGTCAACATTAAC | 51429 |
| rs188268009 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157923860 | GTCAGTTGGATGGCA[A/G]AATGCAGGGAAATGA | 51429 |
| rs188307083 | snp | C/G/T | 0.00343035 | 0.0412724 | intron-variant | SNX9 | GRCh38.p7 | 6:157942758 | GTAATGGGAGTGATA[C/G/T]CTCAACGTTGTTTTG | 51429 |
| rs188348242 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157915987 | AAACTCACTCAATAG[G/T]TCCAGGAGCTTTTTT | 51429 |
| rs188354277 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157933364 | ATCTCCTGTCACTTA[C/T]AGAAGTGGTAGAATT | 51429 |
| rs188382854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157787679 | CGAATTCTGAGAATA[C/T]GGGAAATATTCTATA | 51429 |
| rs188390911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157757855 | GGATTCTGGGTGAAG[A/G]GGTTGGCACCAGCAT | 51429 |
| rs188391146 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157739143 | AGCAAAAGAAACTAT[C/G]ATCAAAGTGAACAGG | 51429 |
| rs188403507 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157715295 | CGCATGCCTGTAATC[C/T]CAGCACTTTGGGAGG | 51429 |
| rs188405450 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157767338 | ACAGTGAGGCCTGGA[C/T]GCCTGTCCTCAGGCC | 51429 |
| rs188421188 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157807019 | CATTCCTACCACTAC[C/G]CTTTCTTGGCTTCAC | 51429 |
| rs188425319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157848664 | TCTTAGGTGGCAGAT[A/G]CCGTGCTACCTGGTA | 51429 |
| rs188427148 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157828314 | TAAAAATGTTGCAGT[A/T]TTTCTACTGTGCCTT | 51429 |
| rs188431460 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889957 | AGGATAATGTTATAG[C/G]CATTGTATAAGTGTG | 51429 |
| rs188442951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157869345 | GCTCCAGCCTCAGAG[A/G]AGGCCAGACACCTTC | 51429 |
| rs188481316 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157801232 | CTTCTTCACTTCTTG[C/T]GAAACCAAACATTAT | 51429 |
| rs188485089 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157756362 | AGGTTGCAGTGAGCT[A/G]TGATTGTTCCTCTGC | 51429 |
| rs188491726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157872158 | AAGTGGGACCTGCCC[C/T]TTAACATTGTTAATA | 51429 |
| rs188495934 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SNX9 | GRCh38.p7 | 6:157831231 | TGATTTGATTTTTCC[C/T]TGAGTTGCTTGTTTT | 51429 |
| rs188526208 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157908193 | TCTCTCTTCCTTCAG[C/T]GCAATCTGTGTGATT | 51429 |
| rs188528235 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157869161 | CACACACCTCTCCCC[A/G]GCCTCACTGGCTGTC | 51429 |
| rs188536172 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | SNX9 | GRCh38.p7 | 6:157942367 | ACAGGCAGGCTCGTG[C/G]TGTCTGCACACTCAG | 51429 |
| rs188548924 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157930795 | TTGGGGACCGTTGCT[C/G]TAAAGTATAAATGAA | 51429 |
| rs188551513 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157815238 | TTTTTTTTTAGACAG[A/C]GTATCACTCTGTTGC | 51429 |
| rs188557004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157906064 | GTAAGTAAATGTAGA[C/T]GAGAGTTGTAAAATT | 51429 |
| rs188569335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157793403 | ATATTCCCCATCCCC[C/T]GCCAAGTTTTTATTC | 51429 |
| rs188573229 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157855762 | TTGAGATGGAGTTTC[A/G]CTCTTGTTGCCCAGG | 51429 |
| rs188583484 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157833747 | TCCCGCCTTCCTAAA[C/G]CATGACTCAGATTTT | 51429 |
| rs188589547 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157876107 | AAGGTTTTAAATTCT[A/G]TCAGGCCTGATGATA | 51429 |
| rs188595640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157936917 | CTTTAAACTATGTGT[A/G]TGGATGCACACATGT | 51429 |
| rs188597561 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157911283 | GCCAGAGAGGCCTGT[A/T]AGAGATGTAAAAGAG | 51429 |
| rs188601580 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157897389 | GGCATGGGGAAGGGA[C/T]GCAGAGCTTCCATGC | 51429 |
| rs188607706 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157929862 | AGTATTACTATTCAA[C/T]CCAGATCTGAAAATC | 51429 |
| rs188638293 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157745542 | CCCTCTGTAATTTGC[A/G]GAGCCAAGAAAAGAA | 51429 |
| rs188642338 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157719830 | CTGAGGTCAGGAGTT[C/T]GAGACCATCCTGACC | 51429 |
| rs188670082 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157760167 | TGAGCCACCACGCCC[A/G]GGCCATCAAGGTTAT | 51429 |
| rs188709797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157747324 | ACAAGATATTTTCAC[C/T]GAATGAAAACAGTCT | 51429 |
| rs188736530 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157827437 | TATATAATATATAAA[C/T]ATATATTATAGTTTA | 51429 |
| rs188744363 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157810988 | GGTGGGAGAATCACT[C/T]GAGCCCAGGAATTCG | 51429 |
| rs188749143 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157786179 | TCCCGAGTAGCTGGG[A/T]TTACAGGCACTTGCC | 51429 |
| rs188778949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157859391 | CTTTTTTGACCATGT[A/G]TTCATTCCATGTCTG | 51429 |
| rs188781809 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157852155 | TCATATGGTAATTCC[A/G]TGTTTAACTTTTGGA | 51429 |
| rs188785055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, nc-transcript-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157892907 | CACAGCGGAAGAGAG[A/G]TAGAGCTGTTAACGG | 51429 |
| rs188792005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157899731 | GGGAGCCAAGATTGC[A/G]CCACTGCACTCCAGC | 51429 |
| rs188800415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157819858 | AGTACAAAGCCTAAA[C/T]AGAGTGGCTCTGTTG | 51429 |
| rs188813863 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157927323 | AATCAGACTAGACTT[G/T]TATGAAATGAGTGGG | 51429 |
| rs188816435 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157860529 | CATTACTTGGTAATC[A/G]TGATGGTACATGTGA | 51429 |
| rs188832983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157839182 | TGAATTGTCCTTGTG[C/T]ATAATTACTGTTATA | 51429 |
| rs188835072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157879377 | TTTTTTTAAAAGGCA[C/T]CTCAGTATGGGTAAT | 51429 |
| rs188852438 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157900367 | TTTTGAATATTAACA[G/T]GTTATCAGATACATG | 51429 |
| rs188861118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157915421 | ATATAAAAATATATC[A/G]TATTTGATTTTCATT | 51429 |
| rs188863087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157932960 | AGTGTGTGTTGCCTG[C/T]TTTCTCCTTAACTCA | 51429 |
| rs188963167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157729870 | CCCCACTGACCTATG[C/T]TACAAGGTGGATAAG | 51429 |
| rs188979009 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157731985 | AAGGCCAAGTCCCCA[C/G]GTCAACAGTTTGAAC | 51429 |
| rs189003263 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157724609 | ACACATCTTCCATAT[G/T]GAATGTGAAATATGC | 51429 |
| rs189005278 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157806291 | CTTTTCCTCCATTTC[C/T]GCATGTGCCATAGGT | 51429 |
| rs189036357 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157854358 | GGGTTAGTAACCTTG[A/C]AGCTGTGATAAAGAA | 51429 |
| rs189044378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157812587 | GCCAGTGTAAAGTGG[A/G]TGTAAATGGTTTCCC | 51429 |
| rs189047982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157771975 | AAGTTCTGGGATTAC[C/T]GGCGTGAGGCACTGC | 51429 |
| rs189054210 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157732740 | GTTTTTAGAGAGGAG[A/G]TCCCACTATGCTGCC | 51429 |
| rs189072493 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157792638 | TAACTAAAGGCACCA[C/T]TTTCTACAATAGATC | 51429 |
| rs189076053 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157879101 | AGCTTTTCGGGGCTG[A/G]TTCGGTAATGTATAT | 51429 |
| rs189081504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157814136 | GAATGCCTTCAACTA[C/T]ATAAGAGCCTTTTAA | 51429 |
| rs189082569 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157914571 | AACCTTGACCTCCCG[G/T]GCTCAAGCAGTCTTC | 51429 |
| rs189104987 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157920681 | TGTCTAGCTTTATAG[G/T]TGCTTTTGAGGGGTA | 51429 |
| rs189109899 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157849611 | GGACTGTGGAACTCA[C/T]ACATGGGATGGAGAG | 51429 |
| rs189244309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157752504 | CTCTGTGTCATAAAC[A/G]AGGTTAAGAAAAAGT | 51429 |
| rs189253206 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | SNX9, LOC107986663 | GRCh38.p7 | 6:157714142 | GAAGAGATGTTCTAT[C/T]TGCCAGGAGCTCCAC | 51429 |
| rs189254967 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157725727 | GAGATTACGGATAGA[C/T]GCAGATAACTTCAGA | 51429 |
| rs189257760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157904358 | AGAATCGCTTGAACC[C/T]GGGAGACGGAGGTTG | 51429 |
| rs189280761 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157921426 | TTGCTAAATAGCTTT[C/G]TACCCAATAGCCAGT | 51429 |
| rs189281418 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157756882 | GCTGTGCCAACCTGC[A/G]GCCGAGGGCCAGATC | 51429 |
| rs189283157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157774558 | GTCTGCCTTAGGAAT[A/G]GCCCCGTCTGCAACA | 51429 |
| rs189286948 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | SNX9 | GRCh38.p7 | 6:157937735 | TAAAAATCTGTACAT[A/C]ACCTCAGGCATGAGT | 51429 |
| rs189291858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157792287 | CTGGGACTACAGGCG[C/T]GCACCACCACACCCA | 51429 |
| rs189291974 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157720534 | GCCTGGGACCCAGCT[G/T]GGCTCATGAGACACA | 51429 |
| rs189299118 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157737863 | TTGTGTCTTTGTTCT[C/T]GTTGGTTTCAAATAA | 51429 |
| rs189299216 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SNX9 | GRCh38.p7 | 6:157819254 | ACATTAGACATTTAT[C/T]TGTAGTTTATTGACT | 51429 |
| rs189302678 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157797860 | ATAAAATAGGAATCC[A/G]GAAGTCTATACTGAT | 51429 |
| rs189308111 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157754164 | AGCCTCCAGCTGCAC[G/T]ACTCCTAAATCATAA | 51429 |
| rs189309833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157838167 | ACAGGCATGCATCAC[C/T]ATGCCTGGCTAATTT | 51429 |
| rs189311752 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157832692 | GTGCCGAGCAAAAGG[A/G]GGAAAACCCTTATAA | 51429 |
| rs189315240 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157795906 | CAAAGCTAGCCAGTT[A/C]CTGGACAAAAGTTAT | 51429 |
| rs189336961 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157906434 | TCTTTCAGACTTTTA[G/T]TATTGAACAAATATA | 51429 |
| rs189337609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157873958 | TCCCTCCAAACCGAG[C/T]GAAGGTTCTTGGTAA | 51429 |
| rs189345336 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157839497 | TACTTTGAAAAGTTA[C/G]TTACTGCTTCACTTT | 51429 |
| rs189356087 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157940323 | TAATAGGCTGCATTT[C/G]GGTGATTTATCTGTA | 51429 |
| rs189360193 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157879936 | GTTCTGTAAACCTAG[A/T]TGTCTTATCTGAAGG | 51429 |
| rs189381293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157903293 | ACATATATTTAGACA[C/T]CAAGATCTAGGTCTA | 51429 |
| rs189391402 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157937270 | GATTCAAAGTATGGC[A/T]GTCTTGGGAGTTATT | 51429 |
| rs189506913 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157906973 | ATCTGGTCTTATTCT[A/G]TAGTCTTTGGAAACT | 51429 |
| rs189514228 | snp | C/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890757 | TAATGGAGCTCAGAC[C/G]AGAGTGATTGTATAT | 51429 |
| rs189516159 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157925997 | AGCAAAAAGGGACAA[A/C]CCCCCTCCATCAAGC | 51429 |
| rs189528655 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157940809 | GATGATTAATTGTAA[C/T]TGAGCAGAGAAACCA | 51429 |
| rs189536546 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157749611 | GCAACCTCTGCCACC[A/T]GGGTTCAAGCAATTC | 51429 |
| rs189569584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157783020 | ATTATATGCTGTCTT[C/T]AAGAAAAGCATTTTA | 51429 |
| rs189583820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157826080 | CTTGTTTGTTCTTAC[A/G]TATTAAGGATGTGGT | 51429 |
| rs189588038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157864077 | TAACTTATAAAGAAC[A/G]GAATTTATTCCTCAT | 51429 |
| rs189592197 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821187 | ATTGTTCTGGTGGGA[A/G]AAGCTTGAAGTCTCT | 51429 |
| rs189600423 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157903143 | TCAGAATTTTCAAGT[A/T]CTCCTTCCAGCAGTT | 51429 |
| rs189602717 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157763633 | ACCCGGCTCCATACA[C/G]CTGCCTGATTCCAGC | 51429 |
| rs189604206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157777118 | CAAAAGCAGCCGGGT[A/G]TGGTGGCTCACGCCT | 51429 |
| rs189629076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157861003 | TTTAAAAAATTCCTC[C/T]AAGTGCATTTGTTTC | 51429 |
| rs189629825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157785790 | AGAATACACTTTGTA[C/T]ACCTGCTACTAAAGA | 51429 |
| rs189632672 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157900591 | ATTTATTATTAAGTT[A/T]AGTGAGGGCGGGGGT | 51429 |
| rs189639700 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157804307 | TATGTCCTGGTTTTA[C/T]TTATGAATGGGGCAA | 51429 |
| rs189640950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157925478 | CATTTCCACTCCTGG[A/G]TATGTACTGAATAGA | 51429 |
| rs189653893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887550 | CCTGCTCCGTGTCCT[A/G]GAGAGTCTCTCCACG | 51429 |
| rs189660196 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157930395 | CTGTGTCAAGACTTT[A/G]GTCATAGAGGATGAC | 51429 |
| rs189664552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157911910 | AATGGGGCTGCACTA[C/T]TGGGTAGATAAACAC | 51429 |
| rs189666314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157866995 | TCACTGTCGTGCAGG[C/T]TGGAGTGCAGTGGCA | 51429 |
| rs189676575 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157944830 | CACGGGCTCCTCAGA[A/G]CGTGGTAGCCGACTG | 51429 |
| rs189676712 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157905015 | TAGGTTCTTTACATA[A/G]ATCTTTAATTCCCTT | 51429 |
| rs189827342 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157772426 | GCATCCCTAGAAGAA[A/C]AGAAAATGGGGGCCA | 51429 |
| rs189833158 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157738538 | ATGTGTGTCTTTGCA[C/T]ATCAGATGGGTCTCC | 51429 |
| rs189858118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157776163 | ATTTTGAATAATAGA[C/T]GCCAACCCATACTAG | 51429 |
| rs189863695 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157809332 | AAACAATGAACCCCA[A/T]CCTTTAGCTCACATC | 51429 |
| rs189867582 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157843043 | ACAGCTTAAAGGTTA[C/G]AAGCAAGATAGAGTT | 51429 |
| rs189874043 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157829165 | TTATATTTTTTAAAA[C/T]ATAATCAATTTTACT | 51429 |
| rs189876180 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157789596 | GGATTCAAGTTCTGA[A/C]TGCCATTTATCAGCT | 51429 |
| rs189880843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157884076 | AAGTTTGTGTTCTTA[A/G]CACCGACCACAGGCC | 51429 |
| rs189884629 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157919560 | CCATGTGATTCTTTT[A/T]TGGTAACTTCTCTCT | 51429 |
| rs189891793 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157850579 | TGGGGGAGTCTCTTC[C/T]CTTGGCTTCTCTTTT | 51429 |
| rs189899464 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157849951 | AAGATGGCAGGTGAC[G/T]TTGTCAGAGTGGATG | 51429 |
| rs189902468 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157891309 | GTTGGGATTACAAGT[G/T]TGAACCGCTGCGCCT | 51429 |
| rs189905582 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890912 | CTTGCTTTCTCTCAT[A/G]TTTGCCCATTCCTCC | 51429 |
| rs189911625 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157907527 | CTGACCTTGTGATCC[G/T]CCCACATTGGCCTCC | 51429 |
| rs189919361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157926555 | TGGAGGCTGAGGTGG[A/G]CAGATTGCTTGAGCA | 51429 |
| rs189922367 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157944550 | CACTTTTTGGACTTT[C/G]TGTGTGATTTTTGTT | 51429 |
| rs190074175 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157760152 | CTGGGATTACAGGCG[C/T]GAGCCACCACGCCCG | 51429 |
| rs190079872 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157757399 | TACCGGGGACACGCT[C/T]ATTCACTCAACAAAC | 51429 |
| rs190086846 | snp | C/T | 4.45623e-05 | 0.00472008 | intron-variant | SNX9 | GRCh38.p7 | 6:157935935 | AATATGCATAACTTA[C/T]AACCACTGATAAAAT | 51429 |
| rs190087534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157723392 | TTTCCTTAATCTTAG[A/G]AAACAACATTCTCTT | 51429 |
| rs190087816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157719470 | ATTATCTTGGAATTA[A/G]GCCAAGGACTTAAAG | 51429 |
| rs190088712 | snp | C/T | 0.00557542 | 0.0525036 | upstream-variant-2KB, nc-transcript-variant | SNX9, LOC107986663 | GRCh38.p7 | 6:157714493 | TATCTGCCAACATCT[C/T]GTAAATCCAGGCTCA | 51429 |
| rs190109373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157762211 | CCCACCATCACCTGC[C/T]AACTGGCAGATCTGA | 51429 |
| rs190113143 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157796809 | ATTTAATTAAATGGC[C/T]GCATTCCATAAAGGC | 51429 |
| rs190115460 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157785028 | GAGGCGGGCAGATCA[C/T]GAGGTCAGGAGTTTG | 51429 |
| rs190119537 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157746996 | GCACACAACCTAGAT[C/G]CTTCACATGCACAGT | 51429 |
| rs190123243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157828801 | CTTAATGCGTCTAAG[C/T]ATCACTTCCCCGGGA | 51429 |
| rs190145625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157870018 | ATGCACACCCACAGT[C/T]GCATGCTCACACACA | 51429 |
| rs190160561 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157874269 | CCTTTTCCATACAAC[C/T]GCAACCCCCTATTCA | 51429 |
| rs190173108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157910165 | TAATTAAATACAGCT[A/G]TGAAGAGAGAACCAT | 51429 |
| rs190178136 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157907483 | TAGAGACGGGGTTTC[A/C]CCATATTGGCCAGGC | 51429 |
| rs190181179 | snp | A/G | | | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157944206 | TGCTTTCATTTTTCT[A/G]ACCTAATAATTACGG | 51429 |
| rs190187883 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157941492 | ATAACGAAAACTTAA[A/G]TTTTTCTTACCTCTG | 51429 |
| rs190325996 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157877966 | TGAATAACTTATTTC[A/G]AGCCTGCTACTCTTT | 51429 |
| rs190329433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157744994 | GTGATCCACCCACCT[C/T]GGCCTCGCAAAGTGC | 51429 |
| rs190331760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157728023 | ATGGCCTCAAGTTGT[C/T]GGTAAAATTCAGCTA | 51429 |
| rs190349305 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157782285 | CCTGTGCGTATGCAC[A/C]CTGACCTGTTGATAA | 51429 |
| rs190352540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157913653 | CAGGTTCCCTCGTGC[C/T]GCCCATCCCCCTGGT | 51429 |
| rs190353530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157768901 | AAAAATTAGCCTGCA[A/G]TGGTGGCAGGAGCCT | 51429 |
| rs190354574 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157930832 | CAGTTTTTAAAGGCA[A/G]TGAATTAATTTTGAC | 51429 |
| rs190366793 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157751488 | AAAAAATTAAAATCC[A/G]AATCTCAAATATTGT | 51429 |
| rs190371134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157788364 | CAGCTACAGGATCAT[A/G]AATCATTGAGCTAAG | 51429 |
| rs190381980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157750848 | CATGCAAATGGCCAA[C/T]GGGCATATGGAAAGA | 51429 |
| rs190385827 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157828564 | AGTGGCACGAACACA[A/G]CTCACGGCAGTCTCG | 51429 |
| rs190392418 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157789130 | ACCCAGGAGATGGAG[C/T]TTGCAGTGAGCCGAG | 51429 |
| rs190395632 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157854798 | TAATCTGCTTTTTAG[G/T]TACACTTTGGAGTGT | 51429 |
| rs190399208 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157809054 | CTCTATCAACCAAAG[A/T]AATTGAATTTGTAAC | 51429 |
| rs190405499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157896229 | GCATCTCAGGATGTT[A/G]GGCGTATTTCTCAAA | 51429 |
| rs190429639 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157928991 | ATCATTTTTGCATGT[A/T]TTCAGAGTGCTTGTA | 51429 |
| rs190563856 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157880783 | CTTGGTGTCAAGGCA[A/G]TGAGTTTAGGAGCCA | 51429 |
| rs190573088 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157862028 | ATGTCCTGAGTGGGA[A/G]AGTGTGAGATTGCAT | 51429 |
| rs190576968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157902113 | ATACAAAGTATATAC[C/T]CTACCAAGAGGCAGC | 51429 |
| rs190588356 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157727270 | GGTCAGAGATAATTC[C/T]ACTAGACCAACTCAA | 51429 |
| rs190593408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157935072 | TTTTAAGAAATTAAT[C/T]TCAGTTACTTTTGGA | 51429 |
| rs190593607 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157916236 | AGATGGGGTTTCACT[A/G]TGTTAGCCAGGATGG | 51429 |
| rs190618796 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157768698 | GCAAACCAGAAAAAC[A/C]GAGAAGAAAATTTTG | 51429 |
| rs190650855 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157849745 | TTGGGTGAGTGGATA[G/T]GAGAAGTTCCATCTA | 51429 |
| rs190652772 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157807662 | AGGCCCCAAAGGCTA[A/G]GGGAGGGATTTTAAT | 51429 |
| rs190670129 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | SNX9 | GRCh38.p7 | 6:157815889 | ACCAGGGCCTGTCGG[C/G]GGGTGGGGGGCTAGG | 51429 |
| rs190674003 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157772836 | CTTTGGGTGGAAACA[C/T]GTGGAGGCCACTAGA | 51429 |
| rs190675798 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157747140 | TGGTTCCTAACAGGC[C/T]ATGGACTGGTACAGG | 51429 |
| rs190705609 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157856040 | AGGCGTGAGCCACCA[C/T]GCCCGGCCTGTCATT | 51429 |
| rs190709900 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157897976 | AAAAGATGCTCCTAC[C/T]ACCCGGGAAATTCCA | 51429 |
| rs190772663 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157735378 | TCAGAATGAACATCC[G/T]GTGGAAGTTGACAAT | 51429 |
| rs190804615 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157756230 | CCAGCCTGGGCAACA[G/T]GGTGAAACCCTGTCT | 51429 |
| rs190808580 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157773103 | TATCCTCTAAACACA[G/T]TCAGCCTCCATTGTT | 51429 |
| rs190818779 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157865880 | TGTTCAGTAAATATT[A/G]TTAAATTAGTGCACT | 51429 |
| rs190823001 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157817229 | ACATTGGTACTGAGG[A/T]TCAAGATGAAAGTAC | 51429 |
| rs190828955 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157856415 | TGGCAGGTATTTTAA[C/T]ACTTCATCTGTAAGT | 51429 |
| rs190832939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157836146 | TGTAGAGACAGGGTC[C/T]CTCTATGTGCCCAGG | 51429 |
| rs190832993 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885927 | ATAGACCCTTTGTAC[A/G]TGTTTGGTAGAAAGC | 51429 |
| rs190888077 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157755869 | TCTCAGACATTGCTG[A/G]AGAGGCAGGGACAGA | 51429 |
| rs190912297 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157769897 | AGGAGAGCACCAGGG[G/T]TCTGAAAGCAGAACA | 51429 |
| rs190913541 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SNX9 | GRCh38.p7 | 6:157794018 | GTATATCTTGTTGGT[C/T]AACTAGGCTAAGCTT | 51429 |
| rs190925971 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157728137 | ATGAAGAGATGTTCC[A/C/G]TTAGCTGAAACGATT | 51429 |
| rs190946203 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157876223 | TTGGGAGGCCGAGGC[A/G]GGCGGATCACCTGAG | 51429 |
| rs190963792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157840706 | GAGCTTCAGAAGGAT[C/T]GACACAGTATCCTTC | 51429 |
| rs190970074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157799488 | AGAAGGAGGGCACTA[C/T]TGGAATTTAGTAGGT | 51429 |
| rs190970778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157891847 | GAACAGCAGAGATGT[A/G]GAAAAGTTTGGGGAA | 51429 |
| rs190981471 | snp | C/T | 5.16907e-05 | 0.00508357 | intron-variant | SNX9 | GRCh38.p7 | 6:157927260 | TCAATCCGCACCCTC[C/T]TCCTTTGGCCATCAG | 51429 |
| rs190986328 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157908127 | GGTATACCTTTTTTT[A/C]CTTTTTATGTCTGTC | 51429 |
| rs190989705 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157942314 | TCAAGGAGCAAGAGG[C/G]CCTGGCGCAGAGACC | 51429 |
| rs190998911 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157939280 | GTTCTGTTAGGAACA[A/G]AAGCCACAAAATTGT | 51429 |
| rs191005417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157882662 | TCATAGAAGATGTTC[A/G]TGAAGGAAGTAACTG | 51429 |
| rs191007170 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157917810 | TCCATACATATTCAT[A/T]ACAGAAAAAAATTTT | 51429 |
| rs191011523 | snp | A/G/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157942102 | AAAACCATGTATTTC[A/G/T]TCACTGTCTTTGCAT | 51429 |
| rs191013003 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157739657 | TGCACATGTATGTTT[A/G]TTGAAGCACTATTCA | 51429 |
| rs191047215 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157798124 | GCATCAAAAGAAAAA[A/C]GGGGAGAAAACCTAG | 51429 |
| rs191050877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157758531 | ATGACAAGGGCCTGG[A/G]GAAAAGACACTCTTG | 51429 |
| rs191052397 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157730177 | GTGAACTCTATGCAG[C/T]GTGAATTATATCTTA | 51429 |
| rs191054353 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157777726 | TGCTGGTGCTGTTGC[C/T]AGCAGGTTGAGCCTA | 51429 |
| rs191060332 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157839782 | CAGTCTCCTCTTTAG[G/T]CCTTTCCTCCTGCCC | 51429 |
| rs191077221 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157861613 | AACAGTGGAGTAAGC[G/T]CAAGGTTGAGCAAAA | 51429 |
| rs191077542 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822132 | TGAGCTCAACAAACA[C/T]AAAAATTCACAGAAA | 51429 |
| rs191158135 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157752294 | AAAGAAAGAGACACA[A/G]AGACAAAGTATAGAG | 51429 |
| rs191166304 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157755490 | GACTACTGATAGACT[C/G]TTGGGCATAATTTTA | 51429 |
| rs191197627 | snp | A/C/G | 0.00597247 | 0.0543191 | intron-variant | SNX9 | GRCh38.p7 | 6:157756814 | AAAGAATCTGATTCC[A/C/G]GCCAGCAGAGGGCAG | 51429 |
| rs191199713 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157737459 | GGTGTTTATAGTATT[C/T]TCTGATGGTAGTTTA | 51429 |
| rs191203102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157824181 | TCATTGGCTAGGAGC[A/G]GTGGTTTGCTTGTTT | 51429 |
| rs191231762 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157862829 | TAAATTAGAATGTTT[C/T]CTTAATAAATTCTTT | 51429 |
| rs191239205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157866254 | CCTTACTCCAGCCAG[A/G]ATAGCTTTGTCCTAG | 51429 |
| rs191243848 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157902380 | TAATAATAACAACTC[C/T]CTTTTAAATGTTTTA | 51429 |
| rs191249479 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157926659 | TGGTGGCATGCGCCT[A/G/T]AAGTCCCAGCTACTT | 51429 |
| rs191268483 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157904810 | TCCTCCAGGTCCTGA[A/G]AACACAAATGCTTCC | 51429 |
| rs191272128 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157938439 | CTTAGTGACATTTGT[C/T]AAGAATAGCAACCTT | 51429 |
| rs191396301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157848968 | GAAAATAGTTCAGGC[C/T]GGGTGTGGTAGCTCA | 51429 |
| rs191405325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890469 | TTTAAATTTAGAACG[C/T]TAAACCAGCAAATTG | 51429 |
| rs191408335 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157717705 | GAACTGAGGCTGAGC[C/T]GGGCGTGTTTAAGGA | 51429 |
| rs191411229 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157733063 | CAGGCACAGCTCCAG[A/C]CTTCTGTGGCCACCT | 51429 |
| rs191413502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157869497 | ATTCAGTGAACCAAG[A/G]CCCCCAAGGCTAAGT | 51429 |
| rs191415449 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157906582 | AGTACATGTATGTTA[C/T]CAGAATAAGGTACCC | 51429 |
| rs191420190 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157931888 | ATCAAGCGCGGTGTC[A/G]CTAGAAGTACTTTGT | 51429 |
| rs191435989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157759941 | GGTGTGAACTTGGCT[C/T]ACTGCAACTTCCACC | 51429 |
| rs191437512 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157740424 | TGCCTCATTGGCAAG[C/T]GGACTAGAATCCCAG | 51429 |
| rs191439058 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157925498 | TACTGAATAGAAATG[A/C]AGGCACACAGACACC | 51429 |
| rs191440382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157778514 | CTTGAGTGAGGTGAG[A/G]GAGTAGTAAATCTTG | 51429 |
| rs191452443 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157741857 | AAAGCATCGCATTTC[C/T]GGCGGAGAGCTTCCT | 51429 |
| rs191457161 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157844539 | AATCTTGTAGCCTCC[A/C]GCTACATGACTCCTA | 51429 |
| rs191458244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157777851 | GCAGCTGCTCTCAGC[A/G]GTCAGGTTTATTCAC | 51429 |
| rs191465827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157803190 | GAAAACATCACTCAA[A/G]TAGGAATGTCATGCT | 51429 |
| rs191490480 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886567 | ATATAAATGGTAATG[G/T]TTTACCACCAGTTGG | 51429 |
| rs191498973 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157922433 | TACATTATCAGCCTG[G/T]GAAATAAATTATGAA | 51429 |
| rs191500483 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SNX9 | GRCh38.p7 | 6:157823781 | GGGACGGAAACTTCC[C/T]GCAGCCCGGGGAGGC | 51429 |
| rs191561872 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157927358 | GTAGTCCAATGACAA[A/G]GGAAACATCATTTGT | 51429 |
| rs191616485 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157832016 | TGGGCATTTCAAAAC[C/T]TTCCAATTGATATTT | 51429 |
| rs191627718 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157853744 | GACTGGAAAGAGGAA[A/G]TAGTTATGCCACAAT | 51429 |
| rs191629107 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157812249 | TCAGCTCACATTCCA[A/G]GGGAAGGGATTTTAC | 51429 |
| rs191641297 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157873783 | CTTCTCCCATTCCCA[C/T]AGACAGAGGGGTGTC | 51429 |
| rs191647700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157909344 | ACTAGTCCTTCATCA[C/T]GTGTAGCTTGAGACA | 51429 |
| rs191649178 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893204 | CTGCCAGGCCCTCAG[C/T]ATGATTGCCTTCATT | 51429 |
| rs191654131 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157927772 | TGCTCTGTCACCCAG[A/G]CTGGAGTGCAGTGGC | 51429 |
| rs191688706 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157716964 | CTGCTCAGCAATCCC[A/T]TGCCCGTCTGTCATC | 51429 |
| rs191700259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157721374 | AATCTTAACGGATAG[A/G]CACCATCAGCATTCT | 51429 |
| rs191734170 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SNX9 | GRCh38.p7 | 6:157759420 | ATTAAATGGGTCAGG[C/T]GCAGTGGTTTATGCC | 51429 |
| rs191745544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157844092 | TTTGGCCTGGCTGGT[C/T]TCGAACTCCTGGCCC | 51429 |
| rs191749920 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157802857 | AGTGTACACAAAACT[C/T]GATGAACTTGCAACA | 51429 |
| rs191752863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157798221 | ACCCCCTGTGAGGGC[A/G]CAATGAGACGAACTC | 51429 |
| rs191798777 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157877010 | AAGATTTTAATAAAA[C/G]AATTGTAATGAGGTA | 51429 |
| rs191803399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157912695 | ATGCTATGACATTCC[C/T]GTGGACTCGATAATT | 51429 |
| rs191805551 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157748167 | TTTATTAGTTTTTTC[A/C]TTTTGTTTTTATAGC | 51429 |
| rs191819255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157725232 | ATTTCGTTCTTATCA[C/T]GGGTTCTGAACAGTT | 51429 |
| rs191822102 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157942560 | GGAGCATGTGTAGAC[A/G]CCTCCCGGCGGGAAG | 51429 |
| rs191827092 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157836833 | CCTGACCTCGTGATC[C/T]GCCCACCTTGTCCTC | 51429 |
| rs191829067 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157786959 | CGTGTATCAATTTGG[C/G]CTACAGGGTGCCCAG | 51429 |
| rs191835636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157806695 | TTCTGAAATTTAAAT[A/G]CAGTTGTCATGGCAA | 51429 |
| rs191837094 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157858224 | GCACATGAACTCGTC[C/T]GGAGTCTTTTTTCTT | 51429 |
| rs191837279 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | SNX9 | GRCh38.p7 | 6:157766409 | CGTGCTCCCCACCTT[A/G]CACTGAGGTGCGTGG | 51429 |
| rs191841853 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157818204 | GGAGCTAGGAGAGCC[A/G]GTCTGAGTCCCAAAA | 51429 |
| rs191857404 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SNX9 | GRCh38.p7 | 6:157827660 | TTTAAAAGATCAAGT[C/T]CTGGAAAAGAAATGA | 51429 |
| rs191959516 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157715898 | AGCAACCCTCATGAC[A/G]AAATTGGTCAGCCCT | 51429 |
| rs191975061 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157752783 | GTCGGGCTGGGGGAC[A/G]GTCACGTCTTTCCCT | 51429 |
| rs191999313 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157790482 | GGTACAAAAATCATA[C/T]CCGACAGTCCTTATT | 51429 |
| rs192018102 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157830703 | AGTGTGACTGAGGAA[A/C]TGTGTTTAAATTTTA | 51429 |
| rs192018554 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157784507 | GTAGCTGGGATTACA[A/G]ATGTGTACCACCACA | 51429 |
| rs192020003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157871925 | GGGATTACAGGTGTG[A/G]GCCACTGTACCCAGC | 51429 |
| rs192020354 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157901473 | GTTGTGTGGTTTCAG[A/G]TCTTCCATTTAGGTC | 51429 |
| rs192027314 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157746108 | TGTTGGAATTGATCA[A/G]TGGCATCCTGCAGAT | 51429 |
| rs192034465 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157933997 | CTGTTGACTGGCTTT[C/T]CTCCCATTACAAAGG | 51429 |
| rs192035126 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157753358 | GGGGATTTAGTCTCA[C/T]ATAAAAAGAAGTTCA | 51429 |
| rs192037226 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SNX9 | GRCh38.p7 | 6:157730471 | GCAGAGGTTGCAGTG[A/G]GCTGAGATCGTGCCA | 51429 |
| rs192056865 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157791513 | ATGTATCTTGAATAA[A/G]TAAATGAGAATCATG | 51429 |
| rs192059825 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | SNX9 | GRCh38.p7 | 6:157826926 | TATAAAATATATTAT[A/G]GTTTATATAATATAT | 51429 |
| rs192060584 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157883632 | ATCTTTAAGTTATGT[A/G]TTTGTCTCCAGGCAA | 51429 |
| rs192066673 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157863686 | GAGGCCAGCACCTCT[C/G]TCTGTTTGGATACTG | 51429 |
| rs192067206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157811075 | ACAAAAAACAAAAAA[C/T]AAAAACTATAGTTTG | 51429 |
| rs192069745 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157903082 | TAAGGCTGTAGTCTA[C/T]GCCAGTGTAGCTTGA | 51429 |
| rs192082009 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157770569 | AAGGCGGGCAGATCA[C/G/T]GAGGTCAGGAGATCG | 51429 |
| rs192092100 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157898542 | GTATGTGGATGGGAT[A/G]TGGCTCATCCTGCTG | 51429 |
| rs192093539 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157918901 | TATGCCATTATTTTT[A/G]TATATATTACATCTG | 51429 |
| rs192099022 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157936183 | TTTTAATTGTGTTTA[A/T]TCATGGTTTCTTAGG | 51429 |
| rs192103406 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157831494 | TTCCTTGCACACAGG[G/T]TTTCCTCTTTACCCT | 51429 |
| rs192113212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157930723 | CCATCCCCCCGACCC[A/G]CTGTCTATCTGTGGA | 51429 |
| rs192233172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157774467 | CCAAGGTGAAGTGGA[A/G]GGTGAGGGGCAGAGC | 51429 |
| rs192264102 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157818850 | GTTCCAGCCTAACAC[C/T]GCCTGCTGCTGCCAC | 51429 |
| rs192275473 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157859056 | AGATAGGTTTTACAC[A/G]TTTCTTAAGTTTATT | 51429 |
| rs192279205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157899496 | GCCCTTTAAAAAAAT[C/T]ATCTATATTTTCACG | 51429 |
| rs192280624 | snp | C/G/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157774563 | CCTTAGGAATGGCCC[C/G/T]GTCTGCAACAGACAG | 51429 |
| rs192282765 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157757204 | GGAAAATATTCAGTC[A/G]TAAGAATCACCATGC | 51429 |
| rs192287100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157737986 | GTTTCTTAATCCTGA[A/G]TTTTAATTTGATTGC | 51429 |
| rs192302805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157819484 | AGAGGAGGTATCCCC[C/T]TGTGCCAGACCCAGG | 51429 |
| rs192321685 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157796352 | AGGCCAGGTTACGAC[A/G/T]TACAAGTTAACCTTG | 51429 |
| rs192325922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157859760 | ACTGTTTGTTCCTCT[A/G]CCCATTTTTGTATTA | 51429 |
| rs192327012 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157810362 | TTGGATGTTTTGTAT[C/G]TCCACTGTGGGGGTG | 51429 |
| rs192334051 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157770517 | TATTGGCCGGGTGCG[A/G]TGGCTCACGCTTGTA | 51429 |
| rs192335665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888684 | CAAACTTGAACACAA[A/G]AGGAAATAAACATTT | 51429 |
| rs192337575 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157838459 | AGGTGTACGGTTGCT[A/G]TGGTAAAAGTATGTA | 51429 |
| rs192339280 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157923687 | GGAGGACTTTATTGC[A/G/T]TATCAGAACTCATTG | 51429 |
| rs192344120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157879130 | ATGAGTATTTACAAT[A/G]CATATCTCTAAGGCC | 51429 |
| rs192347176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157851577 | GGTATCTCACATAGT[A/G]GAATCATATATTCGT | 51429 |
| rs192350272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157939637 | ACTGGGGCATTCATG[A/G]GAGAAAGAGAAGGAT | 51429 |
| rs192355995 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157880310 | ATTTTCCTTCTTTTC[C/T]CACTTCTTCCCTCCT | 51429 |
| rs192361658 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157916179 | AGCTGGGACTACAGG[C/T]ACCCGCCACCACGCC | 51429 |
| rs192472638 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157731155 | CGTGCCACCACACCC[A/G]GCTAATTTTTGTATT | 51429 |
| rs192517924 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157770761 | AGCCGAGATCGCGCC[A/C]CTGTACTCCAGCCTG | 51429 |
| rs192523603 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157760134 | CCTTGGCCTCCCAAA[A/G]TGCTGGGATTACAGG | 51429 |
| rs192568063 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157779684 | AAATGGGTACAGTCA[C/G]TACACAGAGACTTCC | 51429 |
| rs192571946 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157800805 | CAGATGCTGTTTCCA[A/G]AGGTCTACCACAGCC | 51429 |
| rs192578123 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157863296 | GAATGGATTATGCAC[A/C]TTGTGGGCAGATGTG | 51429 |
| rs192587119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157920567 | CAGATTTCCACCATC[A/G]TCGCCTGAAGTTCAG | 51429 |
| rs192587225 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157942951 | AAACAAAACCAAAAA[G/T]AAAGAGTTGCAAAAA | 51429 |
| rs192595000 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157841952 | ACCCACCTCCACAGT[A/G]ATCCTGGCCCGTTTT | 51429 |
| rs192597981 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157883103 | CCTGATCAGTCAGCA[C/G]TCATGAACATCAAAA | 51429 |
| rs192617757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157928040 | TACGTATGTAATTAT[A/G]GGAAAGATTGTTTAA | 51429 |
| rs192626823 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157724215 | AACAAACAAATGCAT[A/G]GGAAAAGGGAGGGGG | 51429 |
| rs192634351 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157943960 | GTGTACAGAGTCCCC[A/G]GCGCTCTGAGGTTGG | 51429 |
| rs192662007 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157837525 | GTTATTTGTGTGGTA[A/C]GTACCCATACCTAAT | 51429 |
| rs192672509 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157795717 | TTTATAGTAATTCAT[C/T]ATATTATTCCCTCTG | 51429 |
| rs192707755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157914025 | GTAAAATGACTGGGT[C/T]ATTTGGCAAGTATAT | 51429 |
| rs192721009 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157940478 | GCTGGAGTACAGTGG[A/T]GCAATCCCGGCTCAC | 51429 |
| rs192727858 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157795495 | AGGGTATCAGATATT[G/T]TAAAAGAATTATGTT | 51429 |
| rs192731903 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157756473 | GTGCTCTGTAAATTG[A/C]GAAGCTCTACATAAG | 51429 |
| rs192750217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157869230 | GGTTCCCACGTCATT[C/T]CACCTTCAGCCCATT | 51429 |
| rs192766715 | snp | C/T | 0.000313638 | 0.0125188 | intron-variant | SNX9 | GRCh38.p7 | 6:157906102 | GGAAAGTCTTAAGAC[C/T]GATGAACATTTATAT | 51429 |
| rs192771936 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157940192 | TGTGCAGGAGGGAGC[A/G]GGGCAGGGACCCCAG | 51429 |
| rs192808197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157791993 | GCAAAACTCCTTCAT[A/G]TTGTTGCTTGTCTCT | 51429 |
| rs192813186 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157753981 | AGAGATGAAATCATG[A/G]GGAGTCAAAGCTGTC | 51429 |
| rs192849655 | snp | A/T | 0.0260105 | 0.111035 | intron-variant | SNX9 | GRCh38.p7 | 6:157903188 | TTTTGAAATTACTAA[A/T]ACTTTTTCCCAATAT | 51429 |
| rs192851484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157937171 | TCCTTCATGGTGGTA[C/T]TATTTTGGGCCACGT | 51429 |
| rs192857195 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157744995 | TGATCCACCCACCTC[A/G]GCCTCGCAAAGTGCT | 51429 |
| rs192870766 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157825788 | TTAATTGTTCCCAGA[C/G]AGTCAAGTTGGTGCT | 51429 |
| rs192873493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157782921 | AGGTAGAGAAGGGAA[A/G]ATAGGGGAAATAAAA | 51429 |
| rs192876492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157852463 | CATGGTCACTCTCAG[C/T]TTCACAATAAGCACG | 51429 |
| rs192913794 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157737202 | CCTCTTTTTCTATTG[A/T]TTGGAATAGTTTCAG | 51429 |
| rs192927146 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157773660 | CTGCCGTCCAGGGAA[A/G]AGATGATCAATCCCC | 51429 |
| rs192961192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157847857 | TGTTGAAAATAAGGT[A/G]TTAATTTTTATAACT | 51429 |
| rs192964116 | snp | A/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889169 | GGCGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 51429 |
| rs192971385 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157924164 | ATCATGCCACTGCAC[A/T]CCAGCCTGGGCAACA | 51429 |
| rs192985030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157724698 | CCTTGTATAGAAGGA[C/T]GCTGACATTCTACTA | 51429 |
| rs192992166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157806501 | TCTACAACTCTAAAA[C/T]GAATCTCATTTAAAA | 51429 |
| rs193012716 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157847486 | TTGGAAAAGCTGAAT[A/C]ACCCAAATGCTATAT | 51429 |
| rs193029354 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157915119 | TTGTATTTGTTGGTT[G/T]ATTTCTGGATTCTAT | 51429 |
| rs193064098 | snp | A/C/G | 0.00716784 | 0.0595003 | intron-variant | SNX9 | GRCh38.p7 | 6:157760154 | GGGATTACAGGCGTG[A/C/G]GCCACCACGCCCGGG | 51429 |
| rs193071212 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157719579 | CTGGCACTGAGTGAC[A/G]ATAACTCAATTAGAT | 51429 |
| rs193074577 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157801294 | CCAAAGTAGCTGTGC[A/G]TGAGCATTTATATGT | 51429 |
| rs193089612 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157872446 | ACTGCTTAGGAATCT[A/G]CAAGTCAGCTTGATG | 51429 |
| rs193097900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157718942 | AAAGTCTTTATTCAC[A/G]CAGTGCCACTGGGGA | 51429 |
| rs193104720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157842756 | AGTGCAGGGTCTGCA[A/G]ATATCTTAATCACTG | 51429 |
| rs193108529 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157908205 | CAGCGCAATCTGTGT[C/G]ATTTTTCTCATTTTC | 51429 |
| rs193119592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157832973 | CCAGACTTTGCCTTG[C/T]CAGATCCCAGATATT | 51429 |
| rs193122104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157792540 | TAAATGAAACTAACA[C/T]GTGCACTACTTCACA | 51429 |
| rs193124953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157874096 | AGAAAAGAATTCCCC[C/T]CAGAGGATGTTTACC | 51429 |
| rs193127836 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157902537 | GAGAGACGCATCGAG[A/T]GTTCCAGTCAGGAAG | 51429 |
| rs193130828 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157936117 | TTAAAACCTGTCTTA[C/G]GACAAACGTCCCAAA | 51429 |
| rs193193350 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | SNX9, LOC107986663 | GRCh38.p7 | 6:157714296 | CAGAAATGCAATACC[C/T]CATTGACTTGTATTA | 51429 |
| rs193194513 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157747659 | TGTTACTAAGTGACA[C/T]CTCGTCAACACTTGC | 51429 |
| rs193204186 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157786516 | TTGTAGATAACAGAT[C/T]GTATATATAGAAAAT | 51429 |
| rs193207424 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157827481 | CTTATAGTTTATATA[A/T]TATATAAACTTATAG | 51429 |
| rs193209102 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157868264 | TAAAAAGCATTTCTG[C/G]ATCTTTACCAAACCC | 51429 |
| rs193219615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157932569 | CCAAGTCTTCCTGTG[A/G]CAGAGGCCAGATTTG | 51429 |
| rs193263250 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157742889 | TAAGCTCTCCCTGAG[G/T]CCTACAACTCTGACT | 51429 |
| rs193276751 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157813623 | GATACTGTCAAAAGA[C/T]GCAATTACAACAAAT | 51429 |
| rs193279538 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157918406 | TGTACTTGTCTAATA[C/T]TAATATAGCCACTCC | 51429 |
| rs193281015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157854710 | CTGAAATTATTGGTT[C/T]TCAGAATGAAAAGTC | 51429 |
| rs199498727 | snp | C/T | 0.000118875 | 0.00770865 | intron-variant | SNX9 | GRCh38.p7 | 6:157927251 | TCTTTCTTCTCAATC[C/T]GCACCCTCCTCCTTT | 51429 |
| rs199551217 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157820671 | ATTGTGAAAGTGCAC[A/G]TGTTTATCTCTTTTT | 51429 |
| rs199554067 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157897479 | AAGGATTTTTACGGC[A/G]GTTTCATCACATAGG | 51429 |
| rs199568656 | snp | A/C | 1.75984e-05 | 0.00296629 | missense | SNX9 | GRCh38.p7 | 6:157936015 | GAAAGACTTATGAAG[A/C]AATTGCCAGTCTCGT | 51429 |
| rs199569684 | snp | C/T | 3.29924e-05 | 0.00406142 | missense | SNX9 | GRCh38.p7 | 6:157940973 | TGCAATTTTACGAAA[C/T]GGTGAGTGGGCGTCC | 51429 |
| rs199591426 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157739828 | CTGAAAACCATCATT[C/T]TCAGCAAACTAACAC | 51429 |
| rs199600712 | snp | C/T | 0.000148301 | 0.00860978 | intron-variant | SNX9 | GRCh38.p7 | 6:157940873 | ATTGATGTTCTGATT[C/T]GGGTTGTAGCTGAGA | 51429 |
| rs199646870 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157934798 | CATGATTTCCTTCTT[-/A]AAAAAAAAATACAGT | 51429 |
| rs199686481 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157939278 | GTGTTCTGTTAGGAA[A/C]AAAAGCCACAAAATT | 51429 |
| rs199732929 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157834513 | CACCCCCCCGGCCAA[-/T]TTTTTAAATTTTTTT | 51429 |
| rs199745971 | in-del | -/GTTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157759844 | ACCTATGCCATCAAA[-/GTTT]GTTTTTTTTGTTTGT | 51429 |
| rs199769737 | in-del | -/TA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157723324 | ACCTCTAAACTCTTT[-/TA]AAAGTAGACAGGGCA | 51429 |
| rs199788699 | in-del | -/TAG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157851539 | CCCCCATTCTACTTT[-/TAG]CTGGCTTCATTTGCC | 51429 |
| rs199793280 | in-del | -/T | 0.0126979 | 0.078662 | intron-variant | SNX9 | GRCh38.p7 | 6:157804617 | AGGGGAACATCAGTC[-/T]TTCCCTTAAGGTTTT | 51429 |
| rs199796163 | snp | C/T | 0.0334219 | 0.124876 | intron-variant | SNX9 | GRCh38.p7 | 6:157938793 | GTGGAAGTTTTTTTT[C/T]CCCCAGCAAAGTTTC | 51429 |
| rs199843915 | snp | A/C/T | 0.000130068 | 0.00806344 | intron-variant | SNX9 | GRCh38.p7 | 6:157873090 | TTTTTTTTTTTTTTG[A/C/T]TGACTTATTAGGATG | 51429 |
| rs199849927 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157752069 | GGTGTCACATGCCTG[A/T]AATCCCAGCTGCTCT | 51429 |
| rs199858007 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157915642 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 51429 |
| rs199870452 | snp | A/G | 0.123452 | 0.215605 | intron-variant | SNX9 | GRCh38.p7 | 6:157769035 | ACAGAGCAAGACTCC[A/G]TTCCAAAAATAAATA | 51429 |
| rs199936941 | snp | C/T | 0.000119389 | 0.00772529 | intron-variant | SNX9 | GRCh38.p7 | 6:157897034 | TCCCACCCTGCCCGC[C/T]CATGGCTGAGTGGGA | 51429 |
| rs199981713 | in-del | -/TTC/TTCC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840420 | ACTTTCTTTCTTTCT[-/TTC/TTCC]TTTCTTTCTTTTCTT | 51429 |
| rs199992874 | snp | A/G | 3.69857e-05 | 0.00430017 | intron-variant | SNX9 | GRCh38.p7 | 6:157936066 | AATCACACAATTCCA[A/G]TTAAGATTTGTTGCT | 51429 |
| rs199999075 | in-del | -/TTG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157844592 | CTAATCCTTGTTTTT[-/TTG]TTTTTTTGTTTTTTT | 51429 |
| rs200012360 | in-del | -/GC | 0.0225045 | 0.103662 | intron-variant | SNX9 | GRCh38.p7 | 6:157768356 | CAGGTCAGGACCTCA[-/GC]GCAGCAGTCAACACC | 51429 |
| rs200014910 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157794962 | TTTGGAAGAGCAGAA[-/T]TTAAAAAAAAAAAAA | 51429 |
| rs200015429 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157782702 | GACCAGCCTGGCCAA[C/G]ATGGTGAAACCCCGT | 51429 |
| rs200025160 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157935580 | AGAAACGCATCAGTT[C/T]TGTGCCGTATGGACC | 51429 |
| rs200039458 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157735247 | GACAGAGCAAGACTC[C/T]GTCTCAAAAAAAAAA | 51429 |
| rs200056638 | snp | C/T | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157892972 | CCGAGCCCCTCCATT[C/T]CACAGCCGGTCCTTG | 51429 |
| rs200068634 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157824846 | TTTTAAAAATAAAAC[-/T]TAGGCCAAGGATTTC | 51429 |
| rs200070924 | in-del | -/AAC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157741351 | GACTCTGTCTCAAAA[-/AAC]AACAACAACAACAAA | 51429 |
| rs200072528 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157831231 | TGATTTGATTTTTCC[-/T]TGAGTTGCTTGTTTT | 51429 |
| rs200078270 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157914463 | TTGGCTTGTCATTTT[C/T]TTTTTCTTTTTTTTT | 51429 |
| rs200099064 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157915670 | ATACACACACACACA[A/C]AAAAATTAGCCAGGC | 51429 |
| rs200101218 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157834521 | CGGCCAATTTTTTAA[A/T]TTTTTTTTTCTTTAG | 51429 |
| rs200103075 | snp | G/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157891165 | GCCTCCCAAGTAGCT[G/T]GGATTATAGGCTCCT | 51429 |
| rs200115816 | in-del | -/GT | 0.0103295 | 0.0711199 | intron-variant | SNX9 | GRCh38.p7 | 6:157781812 | CAACAGTATCACAAA[-/GT]GTATGTGTGTGTGTG | 51429 |
| rs200115965 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157857454 | AGATATGTGATTACC[-/T]TTTTTAAAAAAAAAT | 51429 |
| rs200128498 | snp | A/G | 0.000230806 | 0.0107401 | missense | SNX9 | GRCh38.p7 | 6:157901990 | GCTGATGCAGGCGGC[A/G]CTCAGCGAGGAAACA | 51429 |
| rs200133039 | in-del | -/GTTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157919954 | TTTGTTTGTTTGTTT[-/GTTT]TATATTTGTCTTCCT | 51429 |
| rs200157494 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157936591 | AGGGGATTCTAAAGA[A/G]CAGGAAAGAATGCTG | 51429 |
| rs200162428 | in-del | -/T | 0.0170251 | 0.090679 | intron-variant | SNX9 | GRCh38.p7 | 6:157724918 | GTGAGTATCCAAGGA[-/T]TTTGGTATCCTCAGG | 51429 |
| rs200176443 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157738454 | TCAGAGACTAGGATT[A/G]CAACCCCTGCTTTTT | 51429 |
| rs200179152 | snp | A/G | | | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157715688 | CGTGGCCTATAAAAA[A/G]AAAAAAAAATCAAGA | 51429 |
| rs200218006 | snp | C/T | 0.00011611 | 0.00761851 | intron-variant | SNX9 | GRCh38.p7 | 6:157940856 | AACTTGAGGGAAAAC[C/T]GATTGATGTTCTGAT | 51429 |
| rs200219596 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157780751 | TCTCTCTCTCTCTCT[C/T]TCCTTCCTTCTTTCT | 51429 |
| rs200273705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157862230 | ATTAAGGACAAATAC[A/G]TCAACATATGTTAAT | 51429 |
| rs200273723 | in-del | -/GTATG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157843386 | GTTAACACATATTTT[-/GTATG]TTATATGTATTACAT | 51429 |
| rs200274119 | in-del | -/GCACCTTGTAAGTATGCAGG | 0.0356815 | 0.128715 | intron-variant | SNX9 | GRCh38.p7 | 6:157910707 | TTGTAAGTATGCAGG[-/GCACCTTGTAAGTATGCAGG]TAGAAAGGGTTTGTT | 51429 |
| rs200289226 | in-del | -/C | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157891028 | CTTTTTTCTTTCTCT[-/C]TTTTTTTTTTTTTTT | 51429 |
| rs200300083 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157753022 | CTTGAGTCGACACAG[C/G]CCATGTTTCTGCGAG | 51429 |
| rs200301161 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157778203 | TTCTGGTCTTCAAGC[C/T]GCATTACTTCAGTCT | 51429 |
| rs200308401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157932741 | GTGTGGTGGTGCATA[C/T]AGGTAGTTGCAACTA | 51429 |
| rs200349768 | snp | A/G | 0.000544532 | 0.0164915 | missense | SNX9 | GRCh38.p7 | 6:157875166 | CGTCGGCTGCCAGCA[A/G]CAATCACCAGGTACG | 51429 |
| rs200351981 | in-del | -/T | 0.0622301 | 0.165053 | intron-variant | SNX9 | GRCh38.p7 | 6:157876071 | GATGTTATTTCTTGA[-/T]TTTTTTTTTTAACTA | 51429 |
| rs200361247 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157746360 | ACTTGTTTCCCCTTT[-/A]AAAAAAAAAACATTA | 51429 |
| rs200361860 | in-del | -/AT | 0.264358 | 0.249587 | intron-variant | SNX9 | GRCh38.p7 | 6:157873589 | ATTTTTATAAGCAAA[-/AT]ATATAAATTTTATAA | 51429 |
| rs200413491 | in-del | -/A | 0.0505692 | 0.150756 | intron-variant | SNX9 | GRCh38.p7 | 6:157857741 | TTTGTCCTGTTTCAG[-/A]AAAAAAAAAATCCTA | 51429 |
| rs200426423 | snp | A/G/T | 0.000131825 | 0.00811767 | intron-variant | SNX9 | GRCh38.p7 | 6:157909661 | TTCTGGAACATTGGC[A/G/T]TAGGTTGGAGATTAT | 51429 |
| rs200427973 | in-del | -/AG | 0.0637235 | 0.166737 | intron-variant | SNX9 | GRCh38.p7 | 6:157914007 | CCTCTTGGGTAAATA[-/AG]AGTAAAATGACTGGG | 51429 |
| rs200444660 | snp | A/T | 1.65269e-05 | 0.00287457 | intron-variant | SNX9 | GRCh38.p7 | 6:157927103 | CCTTACAACATTCTC[A/T]TTTACAGGAATGGAA | 51429 |
| rs200461650 | in-del | -/GT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157878926 | ACAGGCTGTCCTTTG[-/GT]GGGGGAAGGTACTAA | 51429 |
| rs200507006 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157805007 | CATTTACAGATAACC[-/A]AAAAAAATAATTTTT | 51429 |
| rs200513432 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157826769 | TTTATATATATATGA[G/T]ATATAAATATATTAT | 51429 |
| rs200514466 | in-del | -/TGTG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157734219 | TCAGTTTAGGATTTA[-/TGTG]TGTGTGTGTGTGTGT | 51429 |
| rs200538485 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157785177 | TTGAACCTGGGAGGC[A/G]GAGGTTTCAGTGAGC | 51429 |
| rs200550680 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157734218 | CTCAGTTTAGGATTT[A/G]TGTGTGTGTGTGTGT | 51429 |
| rs200566971 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157787463 | TCTCTCTGTGTATAT[A/G]TGTGTGTGTGTGTGT | 51429 |
| rs200574278 | in-del | -/AAATAAAT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157769042 | AAGACTCCGTTCCAA[-/AAATAAAT]AAATAAATAAATAAA | 51429 |
| rs200583483 | in-del | -/AA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157931548 | GAATCTTAGCACCTT[-/AA]AAAGAAACCTTAGGG | 51429 |
| rs200597616 | snp | C/T | 0.00023108 | 0.0107465 | intron-variant | SNX9 | GRCh38.p7 | 6:157896806 | CACAAAAATTCTCCT[C/T]CTTTTTACCCCTCTC | 51429 |
| rs200618824 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157780739 | TCTTTCTTTCTTTCT[C/T]TCTCTCTCTCTTTCC | 51429 |
| rs200642433 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SNX9 | GRCh38.p7 | 6:157903765 | TTTGCTTATAACCTT[A/G]AGGCAAGTTTCGTGA | 51429 |
| rs200644343 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888179 | TTTTGTCTGGACTCT[C/G]TCACATACATGTCTA | 51429 |
| rs200668052 | in-del | -/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157836611 | TCTTTTTTTTTTTTT[-/G]ATACAGAGTCTTACT | 51429 |
| rs200670828 | in-del | -/ACTT | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157845434 | CTTAACTGTTGTCTC[-/ACTT]ACACTTATTTTGACA | 51429 |
| rs200672569 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157729285 | GTAGTTTCTTTAAAA[A/T]GTTTTATTAGAAACC | 51429 |
| rs200700778 | in-del | -/G | 0.0115144 | 0.0749975 | intron-variant | SNX9 | GRCh38.p7 | 6:157773492 | AGTAAGAGGTTCAGC[-/G]TAAGTTTTCCTGAGG | 51429 |
| rs200706308 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157878491 | CTGGAGTGCAGTGGC[A/G]TGATGTCAGCTCACT | 51429 |
| rs200756875 | in-del | -/TTTTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157730202 | ATCTTAGTATAACTG[-/TTTTT]TTTTTTTTAAAAAAA | 51429 |
| rs200770589 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157820639 | AGTTATGTTCAAGAT[-/C]CCCTTCGGTGTGGCT | 51429 |
| rs200773287 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157732431 | TTAAGGTATACTTGA[C/G]AATTGGAAATCATAT | 51429 |
| rs200810812 | in-del | -/TTA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157792949 | CTGTTGTTGTTGTTG[-/TTA]TTTTTGTTTTTGTTT | 51429 |
| rs200825144 | snp | A/C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157915644 | AAAAAAAAAAAAATA[A/C/T]ATATATATATATACA | 51429 |
| rs200882071 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157826767 | GTTTTATATATATAT[A/G]ATATATAAATATATT | 51429 |
| rs200883357 | in-del | -/AATT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157875401 | AAAAGGCAGGGTATT[-/AATT]GAGGGTTGCTTTTAG | 51429 |
| rs200925085 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157780754 | CTCTCTCTCTCTTTC[C/T]TTCCTTCTTTCTTCT | 51429 |
| rs200929046 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157738485 | TTTTTCTTTCCATTT[A/G]CTTGGTAAATATTAC | 51429 |
| rs200933229 | snp | C/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889452 | AAAAAAAAAAAAAAA[C/T]ACACCAAAGGATCCT | 51429 |
| rs200955338 | snp | A/C | 4.95487e-05 | 0.00497714 | intron-variant | SNX9 | GRCh38.p7 | 6:157938770 | GAAAGGGTCCTTATG[A/C]GGTGCTGGTGGAAGT | 51429 |
| rs200966585 | snp | A/C | 8.91575e-05 | 0.00667614 | missense | SNX9 | GRCh38.p7 | 6:157935978 | GGTGAAACAGATCTC[A/C]ATGATGCAATAACAG | 51429 |
| rs200976862 | in-del | -/AG | 0.00676609 | 0.0577691 | intron-variant | SNX9 | GRCh38.p7 | 6:157782050 | TGTGGCCATGAGGAC[-/AG]AGTCAGCACCAAGAT | 51429 |
| rs200994695 | snp | C/T | 6.60655e-05 | 0.00574703 | intron-variant | SNX9 | GRCh38.p7 | 6:157937563 | GAAGACAACAGCAGG[C/T]GAAGGAGGCAGATGT | 51429 |
| rs201001295 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157735042 | TTTGGGAGGCCCAGG[G/T]GGGTGGATCACCTGA | 51429 |
| rs201008052 | in-del | -/TAT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157896714 | TTTTGAATACATTTC[-/TAT]TAATTGTTTTTAGTA | 51429 |
| rs201023488 | in-del | -/CACT | 0.0138799 | 0.0821421 | intron-variant | SNX9 | GRCh38.p7 | 6:157826615 | CAGTTTAAGTGTATA[-/CACT]CACTCAGTGCAATCA | 51429 |
| rs201037267 | in-del | -/TATATTATAAATA | 0.0588605 | 0.161139 | intron-variant | SNX9 | GRCh38.p7 | 6:157873472 | TTTGCTAATATTATC[-/TATATTATAAATA]TATATTATAAATATA | 51429 |
| rs201040471 | in-del | -/AAT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157934994 | GTGAGCATTAGTGAA[-/AAT]AATAATTAATGTGGA | 51429 |
| rs201048637 | snp | G/T | 4.98045e-05 | 0.00498997 | intron-variant | SNX9 | GRCh38.p7 | 6:157867528 | TGTAACATCCTCTTT[G/T]CCTCTCCACTCCTGA | 51429 |
| rs201051512 | in-del | -/AAATAAATAAATAAAT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157769042 | AAGACTCCGTTCCAA[-/AAATAAATAAATAAAT]AAATAAATAAATAAA | 51429 |
| rs201056203 | in-del | -/TGTAC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157867480 | GAAAGTGAACTGTAC[-/TGTAC]ACCTTTTGTGTTTTT | 51429 |
| rs201070720 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157810134 | TACTTGGCAATAAAT[A/T]AGAATGACCACTGAT | 51429 |
| rs201090236 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157939875 | CTGGCTTTCTCAGCC[C/T]GGAGGGTTTGGGAGA | 51429 |
| rs201103304 | in-del | -/AA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157827536 | TTTATATAATATATA[-/AA]CATATATTATATTAT | 51429 |
| rs201123802 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157857664 | TGTTTTTTTTTTTTT[-/T]CCATGAAAAAGATTG | 51429 |
| rs201152436 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157743730 | TATTTTAATCATAAA[A/T]AAGGCCAGGCATGGT | 51429 |
| rs201178098 | snp | C/T | 3.29489e-05 | 0.00405874 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157901929 | TGACTGGGATGAAGA[C/T]TGGGATGGGCCCAAA | 51429 |
| rs201185729 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157753023 | TTGAGTCGACACAGC[C/G]CATGTTTCTGCGAGC | 51429 |
| rs201196729 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157816209 | GACACGGGAGGTAAC[G/T]GGTAGATCATAACTA | 51429 |
| rs201199619 | snp | A/G | 5.00263e-05 | 0.00500106 | intron-variant | SNX9 | GRCh38.p7 | 6:157932316 | CCTTTAGAGCCTTAT[A/G]TAGACCTGTCACCTG | 51429 |
| rs201216200 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157834499 | TACAGCTGTGTGCCA[-/C]CCCCCCCGGCCAATT | 51429 |
| rs201230080 | in-del | -/AC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157741364 | AAAACAACAACAACA[-/AC]AAAAAAAAAAAAACA | 51429 |
| rs201258249 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157919467 | TGTTTTTTTTCTTCT[G/T]CTACCTTAAATCTTA | 51429 |
| rs201264101 | snp | C/G | | | intron-variant, nc-transcript-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885172 | AAATTGACATCTGTA[C/G]GTTCAGAATATGACT | 51429 |
| rs201265199 | snp | A/G | 8.24722e-05 | 0.006421 | missense | SNX9 | GRCh38.p7 | 6:157901999 | GGCGGCGCTCAGCGA[A/G]GAAACAGTCGTGCTA | 51429 |
| rs201267154 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157882433 | AGCCCTTGGATCGAG[A/G]AGTAATTTTGACTTC | 51429 |
| rs201307228 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157739816 | ACATGGATGAAGCTG[A/G]AAACCATCATTTTCA | 51429 |
| rs201339611 | in-del | -/G | | | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157715614 | AAAAAAAAAAGAAAA[-/G]GGATATCAGTTTTAT | 51429 |
| rs201376713 | in-del | -/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157844594 | AATCCTTGTTTTTTT[-/G]TTTTTGTTTTTTTTT | 51429 |
| rs201377945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157746844 | AGCAAGTATATTCTC[C/T]AAGACAGTGGTCCCC | 51429 |
| rs201386217 | in-del | -/TATGT | 0.0429648 | 0.14013 | intron-variant | SNX9 | GRCh38.p7 | 6:157843387 | TTAACACATATTTTG[-/TATGT]TATATGTATTACATA | 51429 |
| rs201418103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157910057 | CTAAACCCAGGATGA[C/T]AAATAGAAAGACTCC | 51429 |
| rs201428183 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157759853 | ATCAAAGTTTGTTTT[G/T]TTTGTTTGTTTGTTT | 51429 |
| rs201430777 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157741367 | CAACAACAACAACAA[-/C]AAAAAAAAAAACAGA | 51429 |
| rs201441034 | in-del | -/AC | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894803 | CCATCGGTTCTAAAT[-/AC]ACAGTCTCCTTAAGC | 51429 |
| rs201450083 | in-del | -/TAAA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157817875 | GGGAGACTCTGACTC[-/TAAA]TAAATAAATAAATAA | 51429 |
| rs201478051 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157810198 | TCATGCTAAGTAAAA[C/T]AAGCCTGCCACAAAA | 51429 |
| rs201528600 | in-del | -/TCTG | 0.0154538 | 0.0865337 | intron-variant | SNX9 | GRCh38.p7 | 6:157911105 | GCGACAGAGCGAGAC[-/TCTG]TCTCAAATAAATAAA | 51429 |
| rs201554024 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157789160 | GATAGCGCCACTGCA[C/T]TCTGGCCTGGGCCAC | 51429 |
| rs201560211 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157738412 | TCTTTGTCTTTTTTT[A/G]TCTTTGTTGGTTTAA | 51429 |
| rs201562816 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157915658 | ATATATATATATATA[C/T]ACACACACACACAAA | 51429 |
| rs201564832 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157737296 | TCATTTTTTTTTTTG[G/T]TTGGTAGGCTATTAA | 51429 |
| rs201617886 | in-del | -/ACA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157762280 | GCAGTTTTCAAGCGT[-/ACA]GCAGTTCCTTCTATG | 51429 |
| rs201622459 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157819203 | TTCTCTTTATTCCTA[G/T]AAAGATTCTTCAGAG | 51429 |
| rs201634959 | in-del | -/AT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157805014 | AGATAACCAAAAAAA[-/AT]AATTTTTCTTTACGA | 51429 |
| rs201658684 | in-del | -/TC | 0.264632 | 0.249571 | intron-variant | SNX9 | GRCh38.p7 | 6:157873540 | TTATATCTCAATATA[-/TC]TGTTAATATATACAT | 51429 |
| rs201700980 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157805590 | GCTGCCAGGTCCATC[A/G]TGGTCCACCACAAAT | 51429 |
| rs201774118 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157859647 | CCCAAATTGTGGCCG[G/T]GGGGATCTGGCAATG | 51429 |
| rs201775494 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840432 | TCTTTTCTTTCTTTT[-/C]CTTTCCTTTCTTTCC | 51429 |
| rs201794673 | in-del | -/TAT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157875397 | AGAGAAAAGGCAGGG[-/TAT]TATTGAGGGTTGCTT | 51429 |
| rs201798059 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157826768 | TTTTATATATATATG[A/T]TATATAAATATATTA | 51429 |
| rs201819935 | in-del | -/AAGGAA | 0.0376037 | 0.131863 | intron-variant | SNX9 | GRCh38.p7 | 6:157762635 | ATTTAGAGAAGTGAC[-/AAGGAA]AAGGAAAAGGAAAAG | 51429 |
| rs201820067 | in-del | -/GT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157828210 | TGTGTCTTAAGTAGA[-/GT]GTGTGCAGTATTTGT | 51429 |
| rs201826358 | snp | A/G | 9.90802e-05 | 0.00703778 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157942808 | TGCAGAAAAGCTGAG[A/G]CAGGCCCTCAGCCGC | 51429 |
| rs201852101 | in-del | -/A | 0.0119091 | 0.0762411 | intron-variant | SNX9 | GRCh38.p7 | 6:157876081 | CTTGATTTTTTTTTT[-/A]AACTACATAAAAGGT | 51429 |
| rs201872345 | snp | C/T | 0.000131787 | 0.00811641 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157909751 | AGGCTCCAAAATGTA[C/T]GGTCTAAAGAGCTAC | 51429 |
| rs201890708 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157783588 | GAAACCAATAAGATA[C/T]CTAAAAAAGCATCAA | 51429 |
| rs201891337 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157795187 | TTGGGAGGCCAAGGC[A/G]GGCGGATTGCTTGAG | 51429 |
| rs201891848 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157826502 | GAGACTCCATCTCAA[A/G]AAAAAAAAAAAAAAA | 51429 |
| rs201915145 | in-del | -/T | 0.0154538 | 0.0865337 | intron-variant | SNX9 | GRCh38.p7 | 6:157724545 | AGATTAACTGCCTCC[-/T]TTACTGTCTTGTACC | 51429 |
| rs201919620 | in-del | -/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157732716 | GTTTTGTTTTGTTTT[-/G]TTTTGTTTGTTTTTA | 51429 |
| rs201926267 | in-del | -/ATTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157913328 | TTTATTTATTTATTT[-/ATTT]TTGGAGACGGTCTCA | 51429 |
| rs201933962 | snp | A/C | 3.31576e-05 | 0.00407157 | intron-variant | SNX9 | GRCh38.p7 | 6:157937393 | TTCCTTGATTTTCTG[A/C]ATTTCTCTGCCAGTA | 51429 |
| rs201934522 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157820645 | TGTTCAAGATCCCTT[-/C]GGTGTGGCTTATTGT | 51429 |
| rs201936674 | snp | C/G | 0.000873787 | 0.0208837 | intron-variant | SNX9 | GRCh38.p7 | 6:157938760 | AAGGTAAGATGAAAG[C/G]GTCCTTATGAGGTGC | 51429 |
| rs201973956 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157751677 | GCCTTGGGAACATGA[C/T]GCCAAGTGAAATAAG | 51429 |
| rs202014108 | snp | A/G | 0.000143031 | 0.00845547 | intron-variant | SNX9 | GRCh38.p7 | 6:157897044 | CCCGCCCATGGCTGA[A/G]TGGGAGAGACAGGGA | 51429 |
| rs202024245 | in-del | -/ACCTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157931556 | GCACCTTAAAAAGAA[-/ACCTT]AGGGGTCATTTATTG | 51429 |
| rs202054697 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157865459 | TGACGCCCTGAGGGG[-/A]GCCGTCCTGCTGGCC | 51429 |
| rs202062308 | snp | C/T | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157891919 | GTAGGGAGAATGGGG[C/T]ATGCAGCACGAGGCA | 51429 |
| rs202067093 | in-del | -/TTG | 0.0103295 | 0.0711199 | intron-variant | SNX9 | GRCh38.p7 | 6:157854652 | TTCATTGTGTTGCTT[-/TTG]TTGTTGTATTAATAA | 51429 |
| rs202068999 | in-del | -/C | 0.0158469 | 0.0875917 | intron-variant | SNX9 | GRCh38.p7 | 6:157777388 | CATTTAAAAAAAAAA[-/C]AAAAAGGCAAAAGCA | 51429 |
| rs202097194 | in-del | -/TC | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157891023 | AAATTCTTTTTTCTT[-/TC]TCTCTTTTTTTTTTT | 51429 |
| rs202109568 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157911496 | ACATGTCAGCACTGC[C/T]GTGGAGTTTGTCCCA | 51429 |
| rs202120721 | in-del | -/A | 0.0119091 | 0.0762411 | intron-variant | SNX9 | GRCh38.p7 | 6:157940303 | TTGATCGATTCTGTT[-/A]AGAGTAATAGGCTGC | 51429 |
| rs202142676 | in-del | -/CCTTAG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157931557 | CACCTTAAAAAGAAA[-/CCTTAG]GGGTCATTTATTGAA | 51429 |
| rs202148809 | in-del | -/TA | 0.144296 | 0.226554 | intron-variant | SNX9 | GRCh38.p7 | 6:157826755 | TTATATTATAGGTTT[-/TA]TATATATATATGATA | 51429 |
| rs202152516 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157743427 | GCAAAAAAAAAAAAA[A/C]AAAAACAAAAACGGG | 51429 |
| rs202167517 | snp | C/T | 0.000803718 | 0.0200303 | intron-variant | SNX9 | GRCh38.p7 | 6:157906101 | AGGAAAGTCTTAAGA[C/T]TGATGAACATTTATA | 51429 |
| rs202188324 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157738499 | TGCTTGGTAAATATT[A/C]CTCCATCCCTTTATT | 51429 |
| rs202195603 | snp | A/C/T | 8.37281e-05 | 0.00646977 | missense, synonymous-codon | SNX9 | GRCh38.p7 | 6:157896961 | TCCCAACAACTGGGA[A/C/T]ACTGCCTTCGGCCAC | 51429 |
| rs202231815 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157904432 | AGAGACTCTGTCTCC[-/A]AAAAAAAAAATAAAA | 51429 |
| rs202237884 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157723519 | AAACTCGGTTTCTTG[C/T]CATTTAAGTTTCTCA | 51429 |
| rs207467543 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157834203 | GTCAGGGTCTCTCTT[C/T]TGTTGCCCAGGCTGA | 51429 |
| rs367555501 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157907963 | GGCTCTCCCTGAGGG[C/G]GTTATAGTAATTGTT | 51429 |
| rs367558095 | snp | C/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157892094 | AAGAGGATGAAGATG[C/G]TGCTCAGTAGAAAGG | 51429 |
| rs367576513 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157848492 | TAATGATTGCCTGTT[A/G]AAGTATTGGCTTTTG | 51429 |
| rs367595600 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157732825 | ATAGCTGGGGTTATA[C/T]GCATGAGCCACTGTG | 51429 |
| rs367606391 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157766706 | AGTTCTGTATGAGGG[A/G]CTTCTGGACACTTGG | 51429 |
| rs367623022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157882178 | GTCCTTAGAATTATG[C/T]GGAATCTACTCTGCC | 51429 |
| rs367640659 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | SNX9 | GRCh38.p7 | 6:157909817 | CGTTATCAAAAGCAG[A/G]ATCATGTTTGGATCA | 51429 |
| rs367661331 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157914570 | CAACCTTGACCTCCC[A/G]GGCTCAAGCAGTCTT | 51429 |
| rs367664919 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157899080 | AGGAGGAGAGCCCAC[A/G]GGGGAGGAAGGAGAA | 51429 |
| rs367671224 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157923300 | GGTAAGTAGCAGCTC[A/G]TGTAAATAAATGGTA | 51429 |
| rs367672719 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157767551 | TTTCCTCAATCAGCA[A/G]TTTTCCTACTAGGTC | 51429 |
| rs367684754 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157762989 | CAGAGAGCTCTCCTG[C/T]ATCTGCTTTTTAATG | 51429 |
| rs367685339 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157882116 | AATGCGGCTGGTAAC[-/T]TTTATGTTGAAACCA | 51429 |
| rs367689513 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157748483 | ATGCTTGTAATCCAG[A/C]ACTTTGGGAGGCCAA | 51429 |
| rs367709372 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157773828 | TGGGGAGCCAAAGTG[G/T]TGTTTTTGAGCAGGA | 51429 |
| rs367715313 | snp | A/G | | | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822962 | CACGCAGGGTTGCGG[A/G]CCATGGCCTGGGGCG | 51429 |
| rs367741283 | snp | G/T | 5.69687e-05 | 0.00533677 | intron-variant | SNX9 | GRCh38.p7 | 6:157928560 | CACAGCAGTGCTGTT[G/T]CTCCTGCTTATGTGA | 51429 |
| rs367765060 | snp | A/G | 6.77128e-05 | 0.00581823 | missense | SNX9 | GRCh38.p7 | 6:157896971 | TGGGACACTGCCTTC[A/G]GCCACCCCCAGGCCT | 51429 |
| rs367769501 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157904488 | TAATACATTGCTGTC[C/G]TCAAATTTTTCTGTG | 51429 |
| rs367773692 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157844787 | TTTAGTAGAGACAGC[A/G]TTTCACCGTGTTGGT | 51429 |
| rs367781413 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157855337 | GCTATTCTGGGTGGC[A/C]TTGCAGTAAATATGA | 51429 |
| rs367850067 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157722356 | TCTTTTGCAATATTG[A/C/G]TATAAGTGCTCTAGA | 51429 |
| rs367871900 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157810938 | ATCCAGGTGTGGTGG[A/T]ATGCACCTGTAGTCC | 51429 |
| rs367877183 | in-del | -/TTC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157879496 | CTGAATCAAACTCTC[-/TTC]ATTTTCTTATTCAAA | 51429 |
| rs367901061 | snp | A/G | 1.65053e-05 | 0.0028727 | missense | SNX9 | GRCh38.p7 | 6:157937506 | GGCTGCTTCCCTGAC[A/G]TCATTGGCACTCACA | 51429 |
| rs367905255 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157859502 | CCTGTTAGTAGAAGC[G/T]ATATTGGGGTAGCAT | 51429 |
| rs367924871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885341 | CAGTGGTTTTCTAAC[A/G]TCAGTACAGATTCAT | 51429 |
| rs367925171 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157765277 | CCGCTCCCACCACAT[C/T]GCAGAGGTGCATGGA | 51429 |
| rs367946263 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157797722 | AAATAGAGAAAGGCT[C/T]ATTGAAGGACAGAAA | 51429 |
| rs367949668 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157931347 | AAATGTCTCTGGCCT[A/G]AATATTTTTTAAAGA | 51429 |
| rs367950624 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157938272 | CCTGTGTGCACATGC[C/T]GCCCTGTACCTAGCC | 51429 |
| rs367952706 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157870032 | TCGCATGCTCACACA[A/C]ATAGGCAGCACTCAC | 51429 |
| rs367977564 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157900133 | CTTTCTACTTTCTGC[C/T]TCTATAAGTTTTTTA | 51429 |
| rs368026822 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157754563 | CTTTGTTGAAGGTGG[A/G]TCTGTCTGACGTGCG | 51429 |
| rs368030279 | in-del | -/AAAT | 0.117188 | 0.211804 | intron-variant | SNX9 | GRCh38.p7 | 6:157911112 | GCGAGACTCTGTCTC[-/AAAT]AAATAAATAAATAAA | 51429 |
| rs368037071 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157879149 | ATCTCTAAGGCCCAG[C/T]GGTTCTGAGTTCCTC | 51429 |
| rs368045959 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157748602 | GGCATGGTGGTACGC[A/G]CCTGTAGCCCCAGCT | 51429 |
| rs368111347 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157773123 | CCTCCATTGTTTCAT[A/G]TTTACTCTCCTAAGA | 51429 |
| rs368114135 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | SNX9 | GRCh38.p7 | 6:157762890 | TTGAAATTGTCTTCC[A/G]TGGTTAACCTTTGTT | 51429 |
| rs368140199 | in-del | -/TG/TTTG | 0.0894859 | 0.193158 | intron-variant | SNX9 | GRCh38.p7 | 6:157765351 | ATATATTTGTTTTTT[-/TG/TTTG]TTTGTTTGTTTGTTT | 51429 |
| rs368144402 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157835750 | CCTTGTGAAGAAGGT[A/G]CCTTGCTTCCCCTTC | 51429 |
| rs368188192 | snp | C/T | 1.66549e-05 | 0.00288568 | intron-variant | SNX9 | GRCh38.p7 | 6:157875216 | ATGTGGCTGGCTTTA[C/T]GGAAAACAGAGCGTA | 51429 |
| rs368190503 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157874455 | ATAAAGGAATAGTGA[C/T]TACAGATATTCTTGG | 51429 |
| rs368211094 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157718572 | AGTCTTGAATTAAAA[A/C]ATAAAAGCTAGATTG | 51429 |
| rs368219544 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157898233 | ACTAGTAGCAAACCT[A/G]GATTCAATTGTAGAT | 51429 |
| rs368291309 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157813203 | CAATTCTGCCAATTT[A/C]TGTCAGACCCAGTCA | 51429 |
| rs368291430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157904720 | TCTCAAAAAAATAAA[C/T]AAAATAGAGTAATTA | 51429 |
| rs368295319 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157777470 | TATAAAATGAGGCCT[C/T]TTTTAAACAGTCATC | 51429 |
| rs368312212 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157907170 | TAAAGATTTTTTTTT[-/T]CCTGTTTTCTCTGGA | 51429 |
| rs368314691 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157759756 | AAACTTACAAATTGA[A/G]TAGATTATACTAAAA | 51429 |
| rs368324154 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157878431 | ATATGGAAGCCCACC[-/A]ttttttttttttttt | 51429 |
| rs368336268 | in-del | -/GTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157844589 | TGGCTAATCCTTGTT[-/GTT]TTTTTTTTTTGTTTT | 51429 |
| rs368350575 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157780747 | TCTTTCTCTCTCTCT[C/T]TCTTTCCTTCCTTCT | 51429 |
| rs368350933 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157752744 | TCTTCTACTAATCCT[C/G]CTCAGCACAGACCCT | 51429 |
| rs368366569 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157778191 | AATCCTTAGCCTTTC[C/T]GGTCTTCAAGCTGCA | 51429 |
| rs368372905 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SNX9 | GRCh38.p7 | 6:157840124 | GGTGTCTTTGGATCT[C/T]GGGAAAGAGCAGACC | 51429 |
| rs368397474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157939185 | GTTTGAGTGTTTTTG[A/G]GCAGATGAGGGCAGC | 51429 |
| rs368403608 | snp | C/T | 1.65778e-05 | 0.002879 | intron-variant | SNX9 | GRCh38.p7 | 6:157942772 | ATCTCAACGTTGTTT[C/T]GTTTTGCTTTCTTGT | 51429 |
| rs368437552 | in-del | -/CTTGTCATTTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157914452 | GCAGCTGTGGCTTGG[-/CTTGTCATTTT]CTTTTTCTTTTTTTT | 51429 |
| rs368443752 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157765481 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 51429 |
| rs368448800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157817216 | ACAGACAAGACAGAC[A/G]TTGGTACTGAGGATC | 51429 |
| rs368451427 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157793996 | ATGAAATTTTAGAAT[A/G]TTAAAAGTATATCTT | 51429 |
| rs368458306 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157766093 | TGTCTGGGTGTGAGT[A/G]TGATGCTTCATTTTA | 51429 |
| rs368460653 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157865579 | CACCATTTGTTTCTT[C/T]CCAACAGTTTACTAG | 51429 |
| rs368461402 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157789018 | TTTTGTTTGGTGAAA[A/C]CCCATCTCTACTAAA | 51429 |
| rs368462606 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157882507 | AAATAGTGATTCCTC[G/T]GATGGATCTGGGCAA | 51429 |
| rs368558969 | snp | A/G | 0.00011601 | 0.00761523 | intron-variant | SNX9 | GRCh38.p7 | 6:157921504 | TTTAGACAAAGTTGT[A/G]TGTCATTCTTGGTGT | 51429 |
| rs368561496 | in-del | -/AAATAAAA/AAATAAATAAATAAAA | 0.197884 | 0.254993 | intron-variant | SNX9 | GRCh38.p7 | 6:157817899 | AATAAATAAATAAAT[-/AAATAAAA/AAATAAATAAATAAAA]AGCACTTGAGCCCTG | 51429 |
| rs368578514 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157824078 | TGAATAAAATATCAA[A/G]AGGGAAATGACTGTG | 51429 |
| rs368581700 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157775599 | AGTTACCTCCATTTT[C/T]CCCCCAATTGCTTTT | 51429 |
| rs368587013 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157736588 | CTAAATATACAATCA[C/T]GTCATCTGCAAACAG | 51429 |
| rs368591876 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157722863 | CAAAAATTAGCCAGG[C/T]GTGGTGGCAGACACC | 51429 |
| rs368592674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157904349 | TCAGGCAGGAGAATC[A/G]CTTGAACCCGGGAGA | 51429 |
| rs368593661 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157749631 | TCAAGCAATTCTCCT[A/G]CCTCCACCTCCCGAG | 51429 |
| rs368598683 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157912871 | AAAACAGGGAAATAA[A/G]AGTTCCTCTTTTTTT | 51429 |
| rs368599095 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887895 | GGACAGTTGTGGAAC[C/G/T]GGGATTTGAAGCCTG | 51429 |
| rs368607554 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157865430 | ACACCTCAGCATGGC[C/T]GCTTTGTTCTTCATG | 51429 |
| rs368612210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157777774 | TGCTGCTGCACCTGC[A/G]GTGGGATTAGCTGTC | 51429 |
| rs368615568 | snp | C/T | | | utr-variant-5-prime | SNX9 | GRCh38.p7 | 6:157779846 | CAAGAAAAGTCTCCA[C/T]TGCTCGGGGGAGAAA | 51429 |
| rs368618616 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157719153 | AATGGCAGAAAAGCT[C/T]CCGAACCTCCCAGAA | 51429 |
| rs368622935 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157798285 | ATAACCTGAATCTAA[C/T]CATGAGGAAACACCA | 51429 |
| rs368707426 | in-del | -/GGT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157774268 | GAGTGGAGGAGGTGG[-/GGT]AGTGGAGGAGGGATG | 51429 |
| rs368715130 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157757061 | AGGAGCTGGCAGTTA[A/T]GATATTTACCAAGAT | 51429 |
| rs368741674 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157796419 | AACTCTACTGTTGGT[C/T]AGCAAGGCAGTGGGG | 51429 |
| rs368793371 | in-del | -/ATT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157730988 | AAATGTTACTTTGTC[-/ATT]ATTATTATTATTATT | 51429 |
| rs368797944 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157900689 | TTTAACATAACATCT[A/G]TATGCAGAAGTACAG | 51429 |
| rs368800874 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157737295 | CTCATTTTTTTTTTT[G/T]GTTGGTAGGCTATTA | 51429 |
| rs368845239 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157722100 | GCAAGGGGAACTGGG[C/T]GCCACCGGAATTCGG | 51429 |
| rs368936899 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157740777 | CACCGGCTCAGGGCT[A/G]CCCCAGTGACCTGGC | 51429 |
| rs368945152 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157735781 | AAGACCAGCCTGAGC[A/G]AACAGTGAAACCATG | 51429 |
| rs368974115 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157836871 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 51429 |
| rs368982704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157899198 | CTGATGCTGCTTAAT[C/T]ACTTCTTCACTCTCA | 51429 |
| rs368987010 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157729677 | AAAAATCCAGGGCCA[C/T]GCAAGGTGGCTCATG | 51429 |
| rs368990670 | snp | C/G | 1.65102e-05 | 0.00287312 | intron-variant | SNX9 | GRCh38.p7 | 6:157896801 | AAAGTCACAAAAATT[C/G]TCCTTCTTTTTACCC | 51429 |
| rs368994886 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157858052 | ATGCGGGCCTCTTTC[C/T]ATATGGTCTCGGATC | 51429 |
| rs369000960 | snp | A/G | | | downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157945570 | CATCCCCCCGCCCCC[A/G]GTGGGCAGCGTTGAC | 51429 |
| rs369013533 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157805015 | GATAACCAAAAAAAA[A/T]AATTTTTCTTTACGA | 51429 |
| rs369015398 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SNX9 | GRCh38.p7 | 6:157906033 | GCACCCGAAAGACAG[A/G]ACAAGGTTAAAACTG | 51429 |
| rs369026050 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157826847 | ATATATATATTATAT[A/T]TTATATATAAATATA | 51429 |
| rs369120559 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157817695 | AGCCTGGCCAATATG[A/G]TGAAACCCCATCTGT | 51429 |
| rs369127339 | snp | A/C | | | upstream-variant-2KB, nc-transcript-variant | SNX9, LOC107986663 | GRCh38.p7 | 6:157714728 | GGCCTTCCATATATA[A/C]CATATATATTCCAAG | 51429 |
| rs369135924 | snp | A/G/T | 3.32491e-05 | 0.00407719 | missense | SNX9 | GRCh38.p7 | 6:157873156 | GGAGAACGAGGGCTG[A/G/T]TTCCCACAGACTACG | 51429 |
| rs369160759 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157717424 | TGGCCCGCCCTGCTC[A/G]GGTCAGAGTGCATGC | 51429 |
| rs369167674 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157853002 | TGAGTTTTTTTGTTT[A/G/T]TTTGTTTGTTTGTTT | 51429 |
| rs369183108 | in-del | -/CACT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157799161 | TCTTGAAAACTCACT[-/CACT]ATCATGAGAACAGCC | 51429 |
| rs369188988 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157818106 | ACACACACACACATA[C/T]ATATATATACATATA | 51429 |
| rs369201620 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157746165 | AAGTGACTTTTTTGT[C/T]GTTGTTAGGACTAGT | 51429 |
| rs369203900 | snp | A/G | | | utr-variant-5-prime | SNX9 | GRCh38.p7 | 6:157766395 | CCCAGACCATGTTCC[A/G]TGCTCCCCACCTTGC | 51429 |
| rs369204514 | snp | A/G | 3.30218e-05 | 0.00406323 | intron-variant | SNX9 | GRCh38.p7 | 6:157937545 | TGATCGTAGACATTT[A/G]TAGAAGACAACAGCA | 51429 |
| rs369227667 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157831073 | TCATTATAGTTTCTG[A/G]TTCTTTGCTCATATT | 51429 |
| rs369231830 | snp | A/C/G | 0.000179804 | 0.00948027 | intron-variant | SNX9 | GRCh38.p7 | 6:157928737 | TGCACTGGGCTCGTA[A/C/G]GGGGTGATGCAGGCT | 51429 |
| rs369238111 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157731246 | GATCCACGTGCCTCG[A/C]TCCTGAAGTGCTGGG | 51429 |
| rs369300492 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157918499 | GTGTGCCTTTGAAAT[C/T]AAGCTGTTTCTCTTA | 51429 |
| rs369309536 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157776913 | CCACTCTTTATCTGC[A/C]GAAGGGAAATTAAAA | 51429 |
| rs369312719 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157770785 | CAGCCTGGGTGACAG[A/G]GCGAGACTCCTTCTC | 51429 |
| rs369351219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157937195 | GCCACGTCAAAATAA[C/T]TAATTTTACAAACCA | 51429 |
| rs369354313 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157733016 | TTATTTGGCCTGACA[C/G]CCTCTAGGTTCATCT | 51429 |
| rs369373584 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157880722 | TTGAGATCCATTGTT[C/G]TAACAGATTTCCTGT | 51429 |
| rs369386039 | in-del | -/AC/TCTTTA/TTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840406 | CTTTTACAAAAAATA[-/AC/TCTTTA/TTT]CTTTCTTTCTTTCTT | 51429 |
| rs369398771 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157763657 | TTCCAGCAGCCCAAC[A/C]CACCTGTGCCAACTA | 51429 |
| rs369415193 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157899666 | GTAGTCCCAGCTACT[C/T]GGGAAGCTGAGGCAG | 51429 |
| rs369424081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157787513 | TACACATATATAGTA[C/T]GTATATATTTTTTCT | 51429 |
| rs369462394 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157785468 | TTCCAGGATTGTAAG[A/G]TTGGTTTAACATTCA | 51429 |
| rs369490022 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157859832 | ATCAGAAGATTAACA[C/T]TTTGTGATATGAATT | 51429 |
| rs369509853 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157719554 | TTTCCTGCCTCAGTC[C/T]CAGTCTTTCCTGGCA | 51429 |
| rs369535098 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157877281 | AAAAGAAAAAAAAAG[C/G]GGGGGGGGCATCTAG | 51429 |
| rs369547476 | in-del | -/GTTTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157852589 | CTACTTTTTTGTTTT[-/GTTTT]TTTGAGACAGGGTCT | 51429 |
| rs369551770 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157749350 | TACCTTTTGTGGGCC[G/T]CAGTTTCCTCATCTA | 51429 |
| rs369578563 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157858243 | GTCTTTTTTCTTTTT[-/C]TTTTTTCTTTTTTTT | 51429 |
| rs369580060 | snp | A/G | 9.96959e-05 | 0.00705961 | intron-variant | SNX9 | GRCh38.p7 | 6:157938622 | ATACTGTTGCATTTT[A/G]TATTTCACAGGGAGC | 51429 |
| rs369581598 | snp | C/T | | | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157943842 | GCTTGGCTTGGGTGG[C/T]GGGTTCATGGCCAGT | 51429 |
| rs369586290 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157744480 | AGATGAGTGGAGACA[A/G]CCATGAGCAGAAAGC | 51429 |
| rs369623258 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157806726 | CACAACATTTGGATG[A/G]TCTGAAAACTGGGAC | 51429 |
| rs369636496 | snp | G/T | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894172 | TGGAGTGCAGTGGCG[G/T]GATCTCAGCTCATTG | 51429 |
| rs369637187 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157841682 | GTTGAGGAACTGGGA[A/G]GAGGTGTAGAACTGC | 51429 |
| rs369651688 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157789189 | ACAAAGCGAGACTCC[A/G]TCTCAAAAAAAAAAA | 51429 |
| rs369653461 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157871418 | AGAAAAAGATTATGT[A/G]GTAATTTTGTATAAT | 51429 |
| rs369703354 | snp | A/G | 0.000447483 | 0.0149513 | intron-variant | SNX9 | GRCh38.p7 | 6:157927092 | CTCCACTTGAACCTT[A/G]CAACATTCTCATTTA | 51429 |
| rs369705611 | in-del | -/CA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157843378 | CGCAAACAGTTAACA[-/CA]TATTTTGTATGTTAT | 51429 |
| rs369710724 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157767973 | GGCCATGTCTGCTGC[C/T]TCACAGGCCATCAGG | 51429 |
| rs369733143 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157815323 | GCTCAAGCAATCCTC[C/T]CACCTCCCACCTCAG | 51429 |
| rs369736856 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157814464 | CACTTCTTTTGAAAT[G/T]TCCTGATTATTCCAA | 51429 |
| rs369751344 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157780103 | CTCTGGTGACAGGAC[C/T]CCAAGGTCCCGCCTG | 51429 |
| rs369757758 | snp | A/C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157833067 | TCCTCCCTAGGACAG[A/C/T]TGACATTCAGATATT | 51429 |
| rs369778454 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157720073 | AAAAAAAAGAGTCAA[G/T]ACTTGAGCCTCCTCA | 51429 |
| rs369783196 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | SNX9 | GRCh38.p7 | 6:157942750 | GTGAGGTCGTAATGG[G/T]AGTGATATCTCAACG | 51429 |
| rs369783366 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157837026 | TGGTTGGTCCCTAAG[A/G]TCTGTGAGGCCGTAA | 51429 |
| rs369785859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157735010 | GGCCGGGTGGCTCAC[A/G]CCTGTAATCCTAGCA | 51429 |
| rs369790862 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | SNX9, LOC107986663 | GRCh38.p7 | 6:157714996 | TGCAGTGAGCCGAGA[C/T]TGTGCCACTGCACTC | 51429 |
| rs369831434 | snp | C/T | | | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157944155 | GCGGAGGAGCGCTCC[C/T]GTCTCCCACAGGTGC | 51429 |
| rs369850228 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157874890 | AATAAAAATGAAAAT[A/G]CAACCCATTAAAATA | 51429 |
| rs369871638 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157866632 | AAAATCATGGCTGTT[C/G/T]AGGTAACTCGACCAG | 51429 |
| rs369895280 | snp | A/G/T | 6.59559e-05 | 0.00574232 | missense | SNX9 | GRCh38.p7 | 6:157927177 | ATGATATTTTCCACC[A/G/T]TGGAACCAGAGGCAC | 51429 |
| rs369909437 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157781156 | GGTTGAACTTACACC[A/T]TTCATGTTTTTCAAG | 51429 |
| rs369964087 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157766638 | CCTTCTGTGGGGCTC[A/G]GGATGCCAGCTGATT | 51429 |
| rs369980521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157730303 | CCGAGGCAGGTGGAT[C/T]GCCTGAGGTCAGGAG | 51429 |
| rs369985232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157832721 | AAAACCATCAGATCT[C/T]GTGAGAATTCATGAG | 51429 |
| rs369998044 | in-del | AA/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157733480 | GCAAGACTCTATCTC[AA/G]AAAAAAAAAAAATGA | 51429 |
| rs370015368 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157786699 | CAATAAAAAACATGA[A/T]ATACTTTGGGATAAA | 51429 |
| rs370035475 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157867151 | AGAGATGGAATCTCG[C/G]TTTGTTGCTCAGGCT | 51429 |
| rs370053301 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157856407 | TGAAGAAATGGCAGG[G/T]ATTTTAACACTTCAT | 51429 |
| rs370113621 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157821038 | CTCTTTTTAAAACAA[A/C]AACAACAACAAAAAA | 51429 |
| rs370115416 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157783759 | AAGCAATTCTCCTGC[C/T]GCAGCCTCCTGAGTA | 51429 |
| rs370119947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157801857 | TGGCTTCTACCATCC[A/G]AGGCATGTTGTGAAG | 51429 |
| rs370140935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890342 | CAGTCTACTTTCTGA[A/G]GAAATTTAGCTAATG | 51429 |
| rs370153656 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157725294 | GTTTCTTGTGCTTGA[C/G]GTTTCCTTGTGTGGA | 51429 |
| rs370186167 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157833956 | CTGAGCAAGGAGACA[A/G]GAGTTGGACTTAAGT | 51429 |
| rs370220470 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157909315 | AGTCTGTGATAGATT[C/T]GAAATTTTTAAAAAC | 51429 |
| rs370228348 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157871559 | GGGAGGGATAGCATT[A/C]GGAGAAATACCTAAT | 51429 |
| rs370237870 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157915822 | AGAGTTAGACTCTGT[A/C]AAAAAAAAAAAAAAG | 51429 |
| rs370240512 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157868192 | CAGTGGAGTTCTCTT[G/T]GCTGAATTACAAGTT | 51429 |
| rs370256213 | snp | C/G | 5.66364e-05 | 0.00532118 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157928698 | CTGGAAGCGCTGCAC[C/G]GGCCGTAAGTCCACT | 51429 |
| rs370289833 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157938125 | TTGGCAGCTTTTCTA[C/G]CCGCTTCCATCTGAG | 51429 |
| rs370316112 | in-del | -/GGGCAG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157939958 | CTCCTCTAGAGTTGG[-/GGGCAG]GGGCAGGGGCAGGGG | 51429 |
| rs370325935 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157859799 | GTCTTTTTCTTGAGT[C/T]CCAGAAACTCTTTAT | 51429 |
| rs370337983 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157758857 | GGGATGATGGAACCT[A/G]TTGAGTAGGAGACGC | 51429 |
| rs370340001 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157770681 | GGCAGGCGCCTTTAA[A/G]TCCCAGCTACTTGGG | 51429 |
| rs370342297 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157788006 | AGAGCTAATATTATC[A/G]AATGCTTATTATCCA | 51429 |
| rs370350548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157752264 | TTTCTCGTCGGGTGG[A/G]ACGAGAGACTGAGAA | 51429 |
| rs370355267 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157804468 | GGTGAGTGTATCTGT[A/G]TTAGGGTTTTCCCTA | 51429 |
| rs370361709 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157819633 | CCATTAGTTGACCAA[C/G]CATTTAGTTGGGCTC | 51429 |
| rs370369263 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157838724 | TGTTTAGTTTGAGGT[C/G]TCATTTAAAGAGCTC | 51429 |
| rs370388943 | snp | C/T | 1.64784e-05 | 0.00287035 | intron-variant | SNX9 | GRCh38.p7 | 6:157909882 | AGTTGGCATTGGTAA[C/T]CTTTTCTCTTTCCCT | 51429 |
| rs370400890 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157715980 | AGCAGCAGGGGCGAG[A/G]CTCTTTTCTTGCAGC | 51429 |
| rs370427895 | snp | A/G | 3.29522e-05 | 0.00405894 | missense | SNX9 | GRCh38.p7 | 6:157909770 | CTAAAGAGCTACATC[A/G]AATATCAGCTAACAC | 51429 |
| rs370446691 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157765394 | GGAGTCTCGCTCTGT[C/G]GCCCAGGCTGGAGTG | 51429 |
| rs370463563 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157797891 | GCAATGAGATGCTAC[A/C]ATAAATAAGCGTGGG | 51429 |
| rs370469313 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157834761 | TGGGCATGCTCTGGT[G/T]ATGTGACGTTCAACC | 51429 |
| rs370474659 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157727144 | AGACAGGAGGCCAGA[C/T]TGTTCCTGGAACCGA | 51429 |
| rs370485379 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157828556 | TGGAGTGCAGTGGCA[C/T]GAACACAGCTCACGG | 51429 |
| rs370491396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157762933 | AGGGGGACAGGACAC[C/T]TTTTGTCTTTGTGCC | 51429 |
| rs370508681 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157935225 | TCCTTATGGAAGTAT[G/T]TCAGCTAATAAAGAA | 51429 |
| rs370517413 | snp | C/T | 6.62306e-05 | 0.00575421 | intron-variant | SNX9 | GRCh38.p7 | 6:157940990 | GTGAGTGGGCGTCCA[C/T]GTGCCTTTCGCATGT | 51429 |
| rs370544622 | in-del | -/GAAAA | | | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157715598 | AAAGAGTAAAGAAAA[-/GAAAA]AAAAAAGAAAAGGGA | 51429 |
| rs370558283 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157727182 | CTGGCTGTGTTTTCT[C/T]GTGGCCCAATAACGA | 51429 |
| rs370567389 | snp | A/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157891321 | AGTGTGAACCGCTGC[A/G]CCTGGCCAAAAATCA | 51429 |
| rs370576248 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157767481 | ATTATTTTCATGGCG[A/G]CCCTCTAGCAGCCAT | 51429 |
| rs370579030 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157846713 | TCTTTCACCTTACAC[A/G]ATAATTCATGGTTAT | 51429 |
| rs370594498 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157796609 | ACCTAACTGCAAGGG[G/T]GCAAAGAAGTGTGGC | 51429 |
| rs370602482 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157812133 | AGACAGGGAATCATA[A/G]AGCAACCAAGATGGA | 51429 |
| rs370632890 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157765084 | TAATAGATTATCTAA[A/G]AAGGAACAGGAAGAA | 51429 |
| rs370634120 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157941844 | TGGGAGACTAACTTA[C/T]GGGAGGAACTCACCT | 51429 |
| rs370657602 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157865078 | GGCATGGTGGCTCAC[A/G]CCTGTAATCCCACAC | 51429 |
| rs370689710 | in-del | -/TTTCTTTCTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157780737 | TTCTTTCTTTCTTTC[-/TTTCTTTCTT]TCTCTCTCTCTCTTT | 51429 |
| rs370718199 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157865338 | GAGCGAAACAGTCTC[A/T]GGAAAAAAAAAAAAA | 51429 |
| rs370720997 | snp | A/G | 9.88435e-05 | 0.00702937 | missense | SNX9 | GRCh38.p7 | 6:157909683 | GGAGATTATGGCCCA[A/G]TGTGGGTTTATCCTA | 51429 |
| rs370749686 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157903918 | CTCTGAGGCATCTCT[G/T]TCTCTCTGTAGTGCT | 51429 |
| rs370755432 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157718828 | GTCCCAGCCTCAGAG[A/C]CTTGGTTTGCAGAGG | 51429 |
| rs370759416 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157910514 | AGGAAGAAGCTGCCA[C/G]GTTTTCTACTTATTT | 51429 |
| rs370760754 | snp | G/T | | | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157715451 | TTGGGAGGCTGAGGT[G/T]GGAGGATTGCTTGAG | 51429 |
| rs370761171 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157865212 | AGTGTGGTGGTAGGC[A/G]CCTGTAGTCCCAGCT | 51429 |
| rs370784463 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | SNX9 | GRCh38.p7 | 6:157747895 | TAATTAATAGATGTT[A/C]CCAATGTTAATCTTT | 51429 |
| rs370786059 | snp | G/T | 1.65296e-05 | 0.00287481 | missense | SNX9 | GRCh38.p7 | 6:157896900 | AAAGCTCAGAAGGCT[G/T]GGGGGCCCAGCCAGA | 51429 |
| rs370792581 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157773047 | GAAAGTGATGATGTC[A/G]TCACTAAGGCAATTC | 51429 |
| rs370802314 | snp | C/T | 0.000167343 | 0.00914568 | intron-variant | SNX9 | GRCh38.p7 | 6:157873078 | AATCTTTTTCTTTTT[C/T]TTTTTTTTTTGGTGA | 51429 |
| rs370828877 | snp | A/G | 6.59783e-05 | 0.00574324 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157875152 | AGCTCAGGCCAGTTC[A/G]TCGGCTGCCAGCAAC | 51429 |
| rs370873429 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157843215 | AAGAATTGACGAAAA[C/T]GAAAATTGAAAAAGA | 51429 |
| rs370886619 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157777090 | TCTGTTACATAATGA[-/C]CTTTAAAGGAGGCAA | 51429 |
| rs370891800 | in-del | -/TTTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157876078 | ATTTCTTGATTTTTT[-/TTTT]AACTACATAAAAGGT | 51429 |
| rs370892165 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant | SNX9 | GRCh38.p7 | 6:157875035 | GAAAATAATTGCGGC[A/T]CTTTCTCCTATTCAG | 51429 |
| rs370903344 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157753822 | ATTGCAATAGAGAAA[A/G]AGTAATATACGCAGA | 51429 |
| rs370943439 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157731546 | TTGGATTGGTTTCCA[C/T]GTTAATTAAGAAGAT | 51429 |
| rs370947149 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | SNX9 | GRCh38.p7 | 6:157721471 | CAGGCCCTTCTCTAA[C/T]TGCTCCTCCACACTG | 51429 |
| rs370953883 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157751415 | AAACCATATCAGGAG[C/G]TTCTCAAAAAATTAA | 51429 |
| rs370955764 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157805995 | GGCTGGGTATGAAGT[A/G]AGTGCCTGTCGTAGT | 51429 |
| rs370972073 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157796300 | TTAAATTTATATTGG[A/T]TCTGTCAGACCAGAG | 51429 |
| rs370990831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157774987 | CTCTTTCCTATGGCA[A/G]TGGGTAAACAATGGG | 51429 |
| rs370991458 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157774270 | GTGGAGGAGGTGGGG[-/T]AGTGGAGGAGGGATG | 51429 |
| rs371013030 | snp | C/T | 4.99771e-05 | 0.0049986 | intron-variant | SNX9 | GRCh38.p7 | 6:157932313 | GGGCCTTTAGAGCCT[C/T]ATGTAGACCTGTCAC | 51429 |
| rs371066794 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157839766 | ACCCCATCTTGCCCT[C/T]CAGTCTCCTCTTTAG | 51429 |
| rs371126781 | snp | C/T | 3.31868e-05 | 0.00407336 | intron-variant | SNX9 | GRCh38.p7 | 6:157942764 | GGAGTGATATCTCAA[C/T]GTTGTTTTGTTTTGC | 51429 |
| rs371191791 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157859001 | CTCTCCATTTTTTCC[A/G]ATTTTCTGTGTTATT | 51429 |
| rs371194224 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157934343 | GAAGGTAAACTGATT[A/G]TATCTTGTTTTGTAC | 51429 |
| rs371204755 | snp | C/T | 7.91014e-05 | 0.00628844 | intron-variant | SNX9 | GRCh38.p7 | 6:157897031 | AGGTCCCACCCTGCC[C/T]GCCCATGGCTGAGTG | 51429 |
| rs371214810 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157895892 | GATAGGTCCCAAAAC[A/C]AACTGATTTTTTCTC | 51429 |
| rs371218178 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157836883 | GGCGTGAGCCACCGC[A/G]CCCGGCCGAGAACAC | 51429 |
| rs371236343 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157854057 | TCCTCCCCCTTTGGG[A/G]AAGAAGTGAGACCTT | 51429 |
| rs371251083 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157722898 | ATCCCAGCTCCTTGG[A/G]AGGCTCAGGCACGAG | 51429 |
| rs371297245 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157919168 | GTGAATTATCTCATT[A/G]TTTATCTGGGTATGT | 51429 |
| rs371297380 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157900956 | GCCCTGGCAAGATGA[A/G]GGCGTTTATAGCCCT | 51429 |
| rs371310078 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157882246 | GCACATCTGTTTGCA[A/G]TATGATTTACTGAAT | 51429 |
| rs371362296 | in-del | -/GGGCCACAAGATCAGATGCCCAGTTTATTGATCGGGGTGG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157844407 | TCAGTTCCTGGGTGG[lengthTooLong]TGCCAGCTGATCCAT | 51429 |
| rs371401501 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157804130 | TCCCAAAGTGCTCAT[A/G]TTACAGGCGTGATCC | 51429 |
| rs371406934 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157820504 | AAGTGGGTCTCCTCT[A/T]TAACATTCATGAAGT | 51429 |
| rs371411019 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157818116 | ACATATATATATATA[C/T]ATATATATATGAGTT | 51429 |
| rs371428014 | in-del | -/TTTTTTTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157828310 | CACAGTAGAAAAACT[-/TTTTTTTT]NNNNNNNGCAACATT | 51429 |
| rs371444861 | snp | A/G | 0.000100035 | 0.0070716 | intron-variant | SNX9 | GRCh38.p7 | 6:157927081 | TTGACTGTGCTCTCC[A/G]CTTGAACCTTACAAC | 51429 |
| rs371447870 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157759108 | AACAATGATGGTGTT[A/G]AGAGTTTCAAAAGAC | 51429 |
| rs371451754 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157795667 | ATAGATGAAACATGG[C/T]GAAATATTAACAATT | 51429 |
| rs371487573 | in-del | -/GCAAATATTCCTC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157785899 | TTAGTGATATTCCTT[-/GCAAATATTCCTC]GCAAATATTCCTCAT | 51429 |
| rs371519408 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157765250 | TGGGCAAGTATTTGG[A/G]CATGGATATTCCCGC | 51429 |
| rs371550992 | in-del | -/G | 0.00874735 | 0.0655527 | intron-variant | SNX9 | GRCh38.p7 | 6:157819155 | CTAGTCTAATGCCAA[-/G]GGGGAAACCTTATAG | 51429 |
| rs371580704 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157757567 | AGAAGAGTCACCCAA[C/T]GCAAACTGGGAGGGC | 51429 |
| rs371584189 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157792990 | TTGTTCTGTTGCTCA[A/G]ACTGAAGTACAGTGG | 51429 |
| rs371598888 | snp | C/T | 0.000264472 | 0.0114963 | intron-variant | SNX9 | GRCh38.p7 | 6:157921522 | TCATTCTTGGTGTGT[C/T]GCTTGCAGGCCGCTT | 51429 |
| rs371601794 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157911409 | AATTCTCACTGCACT[C/T]GCAAGAGTCGAGAGA | 51429 |
| rs371611996 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157759844 | CCTATGCCATCAAAG[-/T]TTTGTTTTTTTTGTT | 51429 |
| rs371620241 | in-del | -/CCTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840440 | TTCTTTTCTTTCCTT[-/CCTT]TCTTTCCTTTCCTTC | 51429 |
| rs371624147 | in-del | -/CAACAA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157821044 | TTAAAACAACAACAA[-/CAACAA]AAAACTTCTAGAAAT | 51429 |
| rs371628627 | in-del | -/TT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157913548 | GTAAATTCACTCTTT[-/TT]GGTGTACAGTTCTGA | 51429 |
| rs371628728 | snp | A/G | 5.12168e-05 | 0.00506022 | intron-variant | SNX9 | GRCh38.p7 | 6:157927252 | CTTTCTTCTCAATCC[A/G]CACCCTCCTCCTTTG | 51429 |
| rs371633763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157719156 | GGCAGAAAAGCTCCC[A/G]AACCTCCCAGAATGT | 51429 |
| rs371635172 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157784186 | GTCAGAATTCAATGA[A/G]ATAGAAAATAAACAA | 51429 |
| rs371642868 | snp | C/T | 3.30109e-05 | 0.00406256 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157937511 | CTTCCCTGACATCAT[C/T]GGCACTCACAAGGTA | 51429 |
| rs371646541 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157808428 | ATAAAGAGATGGGGA[A/G]AATGTAAACAGGTTA | 51429 |
| rs371660539 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157773780 | GTTGGATTGGAGGAG[G/T]GAGGACGTTAAGAGG | 51429 |
| rs371660604 | in-del | -/AAAGGA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157762658 | GGAAAAGGAAAAGGA[-/AAAGGA]CTCTGAAGAGTGTCC | 51429 |
| rs371661722 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157774238 | GGAGGAGGTGGAGGA[G/T]TGGAGGAGGTGGGGG | 51429 |
| rs371669693 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157722564 | TTTTGCTCCAGCCTA[C/T]AGCATTTTTAGCAAA | 51429 |
| rs371677930 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157810029 | TTCATAGTAACATTA[A/T]TCACTATAACCCTTA | 51429 |
| rs371688997 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157844655 | CTGGAGTGCAGTGGT[A/G]CAATCTCGGCTCACT | 51429 |
| rs371725112 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157780137 | CTCCTGCCTGGCTCT[C/T]TCCTCCACCCTCTCC | 51429 |
| rs371739108 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840434 | CTTTTCTTTCTTTTC[C/T]TTCCTTTCTTTCCTT | 51429 |
| rs371753387 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157716474 | ACACCTGGAGTGGCA[A/G]GGCTGGGCTCATGTT | 51429 |
| rs371770612 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157759785 | AAACAAAAGTAATAA[A/G]CACTTAAAGCTCATC | 51429 |
| rs371788656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157789063 | GTGGGGCGTGGTGGC[A/G]GGCGCCTGTAGTCCC | 51429 |
| rs371790151 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157862278 | GGTCTGTGAAAGTAA[A/G]TTCTGTTTCTTCTGA | 51429 |
| rs371798940 | snp | A/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157892466 | AACAAGATAAAGAGA[A/G]CGTTCCAGGAAAAAA | 51429 |
| rs371800551 | snp | A/G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157915133 | TTATTTCTGGATTCT[A/G/T]TTCTGCTCCATTGAT | 51429 |
| rs371863473 | in-del | -/CA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157813100 | CTACTGTTAGTGAWC[-/CA]ASWGATCTGTGTGCA | 51429 |
| rs371942665 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157791728 | ATATTTCCAGCAGGA[A/C]AAGCTCTTGCATTGC | 51429 |
| rs371942687 | in-del | -/ATATT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157884285 | ATTTTCCATGTAATT[-/ATATT]TGTTGCAAAGGAATT | 51429 |
| rs371955543 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157742281 | AGGGGAAGAGTGTTT[C/G]GGAAGGAAGCTATTA | 51429 |
| rs371957855 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157855612 | TTCTTTTCTGAGTAC[A/C]GTTTTACATTTTAAA | 51429 |
| rs371966440 | in-del | -/A/AA | 0.480382 | 0.097079 | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157715568 | GTGAGACCCTGCCTC[-/A/AA]AAAAAAAAAAAAAAA | 51429 |
| rs371970032 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157904515 | TGTGGTCCATAACAG[C/T]GCCCAAAAATTGAAA | 51429 |
| rs371980112 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157912492 | AAGCAGCAGCCCCTC[A/G]GTGTGAAGAAAGTTG | 51429 |
| rs371985046 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157865623 | CATGGAGAAAGGTTG[A/G]AATTGAATACCATAG | 51429 |
| rs371987906 | in-del | -/AAGAA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157933302 | CCATCTCAAGAAAAA[-/AAGAA]GAAAAAGCATTTGTC | 51429 |
| rs372019683 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157734134 | ATGAATGATGGAAAT[A/C]CATAAATGAAGACGG | 51429 |
| rs372023722 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157728854 | CCTGTAATCCCTGCA[C/T]TTTGGGAGGCCAAGG | 51429 |
| rs372129551 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157861654 | TCACTGATATGCAGT[A/G]GTCCCCCTTTAGTGA | 51429 |
| rs372132544 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157931827 | TTTTCCTAATCCTCA[A/G]CATGAGGATGGTGTC | 51429 |
| rs372186465 | snp | A/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157891409 | AATTTTTTCAAAAAG[A/G]CTCAATTTAGTCTTT | 51429 |
| rs372189295 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157851110 | AAAATACAAAAAAAT[C/T]AGTGGGGCATGGTGG | 51429 |
| rs372235581 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157866630 | TTAAAATCATGGCTG[G/T]TTAGGTAACTCGACC | 51429 |
| rs372256354 | snp | A/G | 6.75516e-05 | 0.0058113 | intron-variant | SNX9 | GRCh38.p7 | 6:157938592 | AACTAATGACTAATC[A/G]TTTCAGCTTTATTCA | 51429 |
| rs372256497 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157899041 | AAAGGACACTCAGGC[C/T]GTTAGAGTAGGGGAG | 51429 |
| rs372258264 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157844980 | GTGAACAAGGACAGC[C/T]TGGAAGTTAGAAGCA | 51429 |
| rs372261246 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157813225 | ACCCAGTCAGACACC[C/T]GAGGCCTCCCTACAG | 51429 |
| rs372275234 | in-del | -/AATT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157896718 | GAATACATTTCTATT[-/AATT]GTTTTTAGTACTCCT | 51429 |
| rs372294094 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157805393 | TGCCTTCTCTACCAT[C/T]GCTGACCATCCTTCA | 51429 |
| rs372300232 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157841577 | TGGGGTGTGGGGATC[A/G]GGGCCAGTGAAGTAG | 51429 |
| rs372307778 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157924632 | TAGTTCTAGACAAAG[G/T]TCATTTCTTATTTAG | 51429 |
| rs372309423 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157942630 | TCATTCGGGGTTAAG[A/G]TCTGTCCAGCAGCAA | 51429 |
| rs372324135 | in-del | -/TTCTT | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157855633 | ACATTTTAAAAACCA[-/TTCTT]TTCTTACTGACTCGT | 51429 |
| rs372348680 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157926443 | AGAAAAGCATTTACC[G/T]TTTTAGAAAACAGAT | 51429 |
| rs372350668 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157904949 | TGCAGGGAGTACTTC[C/G]AAAGAGAGGATGACT | 51429 |
| rs372375168 | snp | A/C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157811055 | AGCGAGACCCTGTCA[A/C/T]CAAAACAAAAAACAA | 51429 |
| rs372380109 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157791699 | GTAATTAGCCCACAT[-/C]AGGGCAACACTTGAT | 51429 |
| rs372390548 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157915642 | AAAAAAAAAAAAAAA[-/T]ATATATATATATATA | 51429 |
| rs372391120 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157720874 | AGTTCAAGACCAGCC[G/T]GGTTGACATAGCAAG | 51429 |
| rs372400734 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157769984 | TGGGCTCAGTGCTTG[A/G]GTAAATGTTGTCACC | 51429 |
| rs372411070 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157764555 | AAGGTCTGAATTGCC[C/G]AGTAGAAGGCAGAAA | 51429 |
| rs372424668 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157849230 | TTTTTAGTCCAAACT[A/G]GAATACTTTCAAGAA | 51429 |
| rs372435694 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157765545 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 51429 |
| rs372437726 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157795131 | TATAAAAACACATCT[G/T]GAGGCGGGGCACGGT | 51429 |
| rs372475663 | in-del | -/TGGGGTAGTGGAGGAGG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157774265 | GGGGAGTGGAGGAGG[-/TGGGGTAGTGGAGGAGG]GATGTGGGAGGGAAG | 51429 |
| rs372476538 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157763397 | GACACAGGTCCCTGC[A/G]GGGAAGTACCTGCTC | 51429 |
| rs372480412 | snp | C/T | 1.65048e-05 | 0.00287265 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157942879 | CCGCGTGCTTTCTCC[C/T]GACTTGGGGCAATGC | 51429 |
| rs372482418 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157782975 | ATATGAAGCCAGTAG[A/T]CTTAAACCATATCAG | 51429 |
| rs372507889 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157880384 | CTCTCTCACTATTCT[A/G]CCCTCTCTAATCGTG | 51429 |
| rs372541232 | snp | A/G | 4.94564e-05 | 0.0049725 | missense | SNX9 | GRCh38.p7 | 6:157901987 | TCAGCTGATGCAGGC[A/G]GCGCTCAGCGAGGAA | 51429 |
| rs372569819 | in-del | -/GA | | | upstream-variant-2KB, downstream-variant-500B | SNX9, LOC107986663 | GRCh38.p7 | 6:157715059 | TAAAAAAAAAAAAAA[-/GA]AGAAGAAGAAGCAGG | 51429 |
| rs372582260 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157725157 | GACAAGAAATCTGCC[A/G]TGAGTCTTGTCTTTG | 51429 |
| rs372597537 | snp | A/G | | | utr-variant-5-prime | SNX9 | GRCh38.p7 | 6:157766509 | GCTCTGCGGAGGCCC[A/G]GTCCTGCTTCTACTG | 51429 |
| rs372610160 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157733880 | GGACAGCCTTTGTGA[A/C]AACCCTCCGGTTATC | 51429 |
| rs372626762 | snp | C/T | 1.65168e-05 | 0.00287369 | intron-variant | SNX9 | GRCh38.p7 | 6:157901883 | TAACTGATGATCTTC[C/T]ATTTTCACCTCTAGC | 51429 |
| rs372631222 | snp | C/T | 0.000140341 | 0.00837561 | intron-variant | SNX9 | GRCh38.p7 | 6:157928584 | TATGTGACTGACGGC[C/T]GCCTTCACCCACAGA | 51429 |
| rs372636174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157939411 | TGCAGGCATTAAGAA[A/G]CCATTAAAAGGGAGT | 51429 |
| rs372648576 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157871521 | CGTCGCACACCAGGG[C/T]CTGTCGTCGGGTGGG | 51429 |
| rs372664198 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157827089 | TATATAATATATAAA[-/C]ATATATTATAGTTTA | 51429 |
| rs372668879 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157733093 | TGAGGGGACTTCCAG[A/C]GTTTCCCAAGGTTCC | 51429 |
| rs372675941 | in-del | -/TTTA | 0.039522 | 0.134904 | intron-variant | SNX9 | GRCh38.p7 | 6:157913302 | ACTATCTATCTATAT[-/TTTA]TTTATTTATTTATTT | 51429 |
| rs372700907 | snp | C/T | 3.35965e-05 | 0.00409843 | intron-variant | SNX9 | GRCh38.p7 | 6:157875010 | ACTCCCTGAAGTGAC[C/T]GTAATCTATGAAAAT | 51429 |
| rs372702440 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157765598 | CTGACCTCGTGATCC[A/G]CCCGCCTCGGCCTCC | 51429 |
| rs372709476 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157798697 | TCTCTAAGCTTGAAT[G/T]CATTTCAAATATTAA | 51429 |
| rs372720329 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157858307 | GCTGGAGTGCAATGG[C/T]GCAATCTCGGCTCAC | 51429 |
| rs372793053 | in-del | -/TGTCTG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157802390 | ATTTCTCTGTGTCTG[-/TGTCTG]ACTTTCCTCGTGTGT | 51429 |
| rs372811102 | in-del | -/CTGCA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157721247 | GATTGCGCCACTGCA[-/CTGCA]GCCTGGGCGACACAG | 51429 |
| rs372852766 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157775574 | TTGACTGACTTTACA[C/G]TGCCCCAGCAGTTAC | 51429 |
| rs372858206 | in-del | -/TA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157806786 | TATGTCAATCTAAAC[-/TA]TATATATATATTTGG | 51429 |
| rs372891010 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157868883 | TTCGTGACACTGCCC[C/T]GTGCATGCCTGTCCT | 51429 |
| rs372896212 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157910295 | ATTGTCTTCATTGCT[A/G]TACCTTTTCTACAAA | 51429 |
| rs372899884 | in-del | -/TAT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157915642 | AAAAAAAAAAAAAAA[-/TAT]ATATATATATATACA | 51429 |
| rs372932316 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157902109 | ATTAATACAAAGTAT[A/G]TACCCTACCAAGAGG | 51429 |
| rs372951512 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157719487 | CCAAGGACTTAAAGA[C/G]AGCAGCAAACCCTTT | 51429 |
| rs372952723 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157863323 | TGTGTGCTTGCACAC[C/T]TGGTATTCTAGTGTC | 51429 |
| rs372960638 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157910960 | CCCTGTCTCTACTAA[-/A]AAATTAGCCCGGTGT | 51429 |
| rs372983146 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157895506 | AAGATAAATGAACAT[C/T]AGCATATACTGGTCA | 51429 |
| rs373005100 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157722542 | ACTGTCTGTGCCTCC[A/C]CAGCCATTTTGCTCC | 51429 |
| rs373007651 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157832372 | ATGTCAGTATGAAAG[C/G]CCTGTCCTTGTACTC | 51429 |
| rs373038670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157865006 | CACTTTAGCCTGGCG[A/G]CAGAGAGAGACTCTG | 51429 |
| rs373042431 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157767103 | GTTCCCCAATAAAGA[A/C]ATACTCAGAGGATCT | 51429 |
| rs373044050 | snp | A/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894494 | AAAAAAAAGCTAACA[A/G]AAAACTGTATTTGCC | 51429 |
| rs373139267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157790054 | CGCCAGGAAGGAGGA[A/G]GGCAGGGAGGACGGG | 51429 |
| rs373149887 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | SNX9 | GRCh38.p7 | 6:157922289 | AGTAAGCATTTACTG[A/T]ACTCCTTATTGTATC | 51429 |
| rs373155198 | snp | C/T | 0.000248051 | 0.0111339 | intron-variant | SNX9 | GRCh38.p7 | 6:157940988 | CGGTGAGTGGGCGTC[C/T]ACGTGCCTTTCGCAT | 51429 |
| rs373168852 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157903226 | CCATGATTCAAGGCA[G/T]ATATCAAAGAATGTT | 51429 |
| rs373192964 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157743905 | ACCTATAGTCCCAGC[C/T]ACTCGGGAGGCTGAG | 51429 |
| rs373227241 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157726752 | CAATAAGGTGAAACA[C/T]GAAGTTTTCTAGTCT | 51429 |
| rs373228671 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157786816 | TGTCTCTAACCTGAG[C/T]TCTGCACGCTATAAC | 51429 |
| rs373230860 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157764878 | TGGAAAATTTGCTGG[C/T]AGCACGTAACATCTC | 51429 |
| rs373237502 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157776735 | ATGTGGCTTGGCTCC[C/T]GTAGGTTTGTTTGCT | 51429 |
| rs373241183 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157796317 | CTGTCAGACCAGAGA[A/G]GAGAGGTGTGAGTCA | 51429 |
| rs373242443 | snp | A/C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157819111 | ACAAACATAATTTTA[A/C/G]AACCATACACTTTTC | 51429 |
| rs373254248 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157865340 | GCGAAACAGTCTCAG[C/G]AAAAAAAAAAAAAAA | 51429 |
| rs373268783 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157933998 | TGTTGACTGGCTTTT[C/T]TCCCATTACAAAGGA | 51429 |
| rs373285046 | snp | A/T | | | upstream-variant-2KB, downstream-variant-500B | SNX9, LOC107986663 | GRCh38.p7 | 6:157715044 | TGAGACTCCGTCTCT[A/T]AAAAAAAAAAAAAAG | 51429 |
| rs373325049 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157735489 | TGAGGTCAGGAGTTC[A/G]AGGCCAGCATGGCCA | 51429 |
| rs373358555 | snp | G/T | 3.46218e-05 | 0.0041605 | intron-variant | SNX9 | GRCh38.p7 | 6:157906105 | AAGTCTTAAGACTGA[G/T]GAACATTTATATTCA | 51429 |
| rs373369513 | in-del | -/GCCTTTGCTCCTG | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888061 | CACCGGGAGACATTG[-/GCCTTTGCTCCTG]TGTTCACAGACCAGC | 51429 |
| rs373378549 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157909200 | TGTTCCTGATCCACC[A/G]TGAGATAGGTACAGT | 51429 |
| rs373382952 | in-del | -/GTGT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157787477 | TGTGTGTGTGTGTGT[-/GTGT]ATTTGTGTGTATATG | 51429 |
| rs373389751 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157868191 | CCAGTGGAGTTCTCT[G/T]TGCTGAATTACAAGT | 51429 |
| rs373414365 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157754987 | GTGAATCTCATGTCT[C/G]CCCTTTTTAGACCAT | 51429 |
| rs373419868 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SNX9 | GRCh38.p7 | 6:157766889 | TTGGGATAAAGCCAC[A/G]TTCAGGGTCTCAGTT | 51429 |
| rs373421073 | snp | A/G | 1.66096e-05 | 0.00288176 | intron-variant | SNX9 | GRCh38.p7 | 6:157942754 | GGTCGTAATGGGAGT[A/G]ATATCTCAACGTTGT | 51429 |
| rs373444362 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157814399 | ATTCATGCCATCCTT[C/T]CTCCTTGAAAACTGG | 51429 |
| rs373451947 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157826849 | ATATATATTATATTT[A/T]ATATATAAATATATA | 51429 |
| rs373453187 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157842785 | TGATCTTAGGTTTTA[A/C]AATAGTGATGTTATC | 51429 |
| rs373503030 | snp | A/G | 0.000725223 | 0.0190285 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157875077 | TGATGGAAAAGATCA[A/G]TTTTCTTGTGGAAAT | 51429 |
| rs373506329 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157726732 | TGAGTGCTGTACCCA[A/G]TGCCCAATAAGGTGA | 51429 |
| rs373518169 | in-del | -/CAGGGG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157939973 | GGGCAGGGGCAGGGG[-/CAGGGG]GGACAGAGAAAGAAG | 51429 |
| rs373550780 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157781759 | TATAGGCAGAAAACA[C/T]CAGCCTTACTGGCTT | 51429 |
| rs373574009 | snp | C/G/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157757731 | ACCTCTTTGCAATGC[C/G/T]CCTTGCACAGCCATA | 51429 |
| rs373585167 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-5-prime | SNX9 | GRCh38.p7 | 6:157716142 | ATAATGACAAGGGTC[A/G]TTGTGTGTTTTGCTG | 51429 |
| rs373589979 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840429 | TCTTTCTTTTCTTTC[C/T]TTTCTTTCCTTTCTT | 51429 |
| rs373592297 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157937418 | CCAGTAACAATCAGC[C/T]TGTATCTTGTTATAG | 51429 |
| rs373595069 | in-del | -/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157774254 | GGAGGAGGTGGGGGA[-/G]GTGGAGGAGGTGGGG | 51429 |
| rs373601340 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157770719 | GGCAGGAGAATGGCA[G/T]GAACCTGGGAGGCAG | 51429 |
| rs373608007 | snp | A/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888949 | GGAGTGTGGTACCAC[A/G]GAGAGAGGGAAAAGA | 51429 |
| rs373612363 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157858447 | GGCTGGTCTCAAACT[A/C]CTGTACTCACGTGAT | 51429 |
| rs373619622 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157729711 | ATAATCCCAGCACTT[C/T]GGGAGGCTGAGGCGG | 51429 |
| rs373631888 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157911419 | GCACTCGCAAGAGTC[A/G]AGAGAAACAGTTCAG | 51429 |
| rs373635657 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157818883 | CTGCCATCCATGCAG[C/T]CTCCCTAGCCTCCAG | 51429 |
| rs373640744 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157828557 | GGAGTGCAGTGGCAC[A/G]AACACAGCTCACGGC | 51429 |
| rs373646683 | snp | A/C/G | 0.000637557 | 0.0178432 | intron-variant | SNX9 | GRCh38.p7 | 6:157867499 | TTTTGTGTTTTTACT[A/C/G]CTCTGTTTGTGTTTG | 51429 |
| rs373648026 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157943571 | TATGTGAGGACCAGT[A/G]CTTTCTCTCTTTGCA | 51429 |
| rs373688320 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157799850 | GAATTCTGGGAGATC[-/C]AATTCAAGTTGAGAT | 51429 |
| rs373693985 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157741163 | ACCAGCCTGGCCAAC[A/G]TGGCAAAATCCCGTC | 51429 |
| rs373716275 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157770516 | TTATTGGCCGGGTGC[G/T]GTGGCTCACGCTTGT | 51429 |
| rs373735277 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157837331 | GCCAGAAAACATGCG[A/G]TACAGTTTTGTGTGT | 51429 |
| rs373735580 | snp | A/G | 1.66521e-05 | 0.00288544 | intron-variant | SNX9 | GRCh38.p7 | 6:157940846 | GTCATTTGAAAACTT[A/G]AGGGAAAACTGATTG | 51429 |
| rs373763332 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157940287 | GACCAAGTATTTTCT[A/G]TTTGATCGATTCTGT | 51429 |
| rs373774268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157914512 | ACAGGGTCTCACTGT[C/T]GTCGCCCAGGCTGGA | 51429 |
| rs373851587 | in-del | -/GTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157792936 | GTTGTTGTTGTTGTT[-/GTT]TTTGTTTTTGTTTTG | 51429 |
| rs373890917 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SNX9 | GRCh38.p7 | 6:157737847 | CAGAGATTCTCATAC[A/G]TTGTGTCTTTGTTCT | 51429 |
| rs373895357 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157810681 | ACCCTTGATGTTGGG[-/T]TTTTTTTTTTTTCTG | 51429 |
| rs373923512 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157906284 | ACTTTAAAGCTAAGC[A/G]AGTTATTCATCTTTT | 51429 |
| rs373924285 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157796545 | ACTGGGGCTTCTCGA[A/C]AGTCACTTTTGCTCA | 51429 |
| rs373986967 | snp | C/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890397 | TTTAAATAAGTCTCC[C/T]AATGTCAAGCCTGCA | 51429 |
| rs373991117 | in-del | -/AAT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157862254 | TGTTAATAGCATAAT[-/AAT]GCTCAGGGTCTGTGA | 51429 |
| rs373994572 | snp | A/G | 4.9458e-05 | 0.00497258 | missense | SNX9 | GRCh38.p7 | 6:157927138 | GGAAAGAGGAAGGCC[A/G]AGAGAGATGAGCTGG | 51429 |
| rs374010599 | snp | A/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894249 | CAAGTAGCTGGGATT[A/G]CAGGCGCCCACCACT | 51429 |
| rs374019407 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157742425 | GTCATGAAGACTCGC[A/G]GTCAAGTTGAGAGTG | 51429 |
| rs374026716 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SNX9 | GRCh38.p7 | 6:157759913 | TTGCTGTGTTTCCCA[G/T]CTGGAGTACAGTGGT | 51429 |
| rs374027534 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157742521 | TGGGAAGACCTTTGG[A/G]TCAAGTCCAGTGGTT | 51429 |
| rs374038005 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157771539 | ATAGCTGCTAACAGG[C/G]AGTTAAATGTTCAGA | 51429 |
| rs374038600 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157865089 | TCACGCCTGTAATCC[C/T]ACACTTTGGGAAGCC | 51429 |
| rs374042748 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157826414 | CTGAGGCAGGAGAAT[A/T]GCGTGAACCCGGGAG | 51429 |
| rs374100084 | snp | A/C/T | 4.94926e-05 | 0.00497436 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157942846 | TGATGTAGGACAGAA[A/C/T]GGGCCTTGAAGAGAA | 51429 |
| rs374100449 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157827522 | ATATAAACATATAGT[A/T]TATATAATATATAAA | 51429 |
| rs374124793 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157769507 | TGCTGAAGTCAAGAC[C/G]TGAAGGCTGAGTAAG | 51429 |
| rs374134997 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157782659 | TTTGGGAGGCCAAGG[C/T]GGGTGGATCATGAGG | 51429 |
| rs374138880 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157845417 | TGCCCGGCCCCATTT[A/G]TCTTAACTGTTGTCT | 51429 |
| rs374146852 | snp | A/G | 0.000132718 | 0.00814503 | intron-variant | SNX9 | GRCh38.p7 | 6:157942765 | GAGTGATATCTCAAC[A/G]TTGTTTTGTTTTGCT | 51429 |
| rs374178360 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157733784 | ACCTCTGAAGGGACC[C/G]CAGGTGGTACAGACA | 51429 |
| rs374179044 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157718966 | CTGGGGACTTCCCTT[A/G]GCCATTGTTGCCTGC | 51429 |
| rs374190155 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157902659 | TAAAACAAAAAAAAA[-/A]GTGTTGTGTTTTATT | 51429 |
| rs374198632 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157877652 | GAGCTGCTTGGGAGG[C/T]TCTGATTGCCTGTGC | 51429 |
| rs374202176 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157844500 | CTCAAGCACTGATCT[C/T]AGGAGCAGTTTAGAG | 51429 |
| rs374203622 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | SNX9, LOC107986663 | GRCh38.p7 | 6:157715181 | CCTATGCCTTCCTCA[C/T]GCTCAGGGACACAAT | 51429 |
| rs374211780 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157792360 | TGGCCAGGATGATCT[C/T]GATCTCTCGTCCTCG | 51429 |
| rs374212489 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157904413 | CACTCCAGCTTGGGC[A/G]ACACAGAGACTCTGT | 51429 |
| rs374217078 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157880669 | CAGTTATTGAGAGGC[A/G]TGCTCTGCATCCTTG | 51429 |
| rs374231197 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157835665 | CGGGGTCGATTTCCC[C/T]CATGCTGACTGAGCT | 51429 |
| rs374236412 | snp | A/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157891573 | AAGAACATCACATTT[A/G]AAATATTTGAGTCCT | 51429 |
| rs374258434 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157826888 | TATATAATATATAAA[-/T]ATATATTATAGTTTA | 51429 |
| rs374286027 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157920658 | CATTTGGTTGTTTTT[A/T]TTACTGTTGTCTAGC | 51429 |
| rs374297037 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157902739 | GTGGTGCGATCTTGG[C/T]TCACTGCAACCCCAA | 51429 |
| rs374309863 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157864448 | TGTTTCCATTTCTTT[C/G/T]TTTCTCACTTGTTTC | 51429 |
| rs374333036 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157808146 | AAGAAACAATTCACC[A/C]CAGACACAATAAACA | 51429 |
| rs374365685 | snp | A/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885974 | TTAATTAAATATGTT[A/G]CCATTTTCATTAATT | 51429 |
| rs374370026 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157716390 | TCATTTATAGTCACA[A/G]TAGCCCTAGGTCCAC | 51429 |
| rs374375479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157759203 | ACGTCAGAAGTCACA[C/T]GGCCCTGGCTGGTAG | 51429 |
| rs374403452 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157924037 | ACCCTGTCTCTACTA[A/G]AAATACAAAAATTCG | 51429 |
| rs374403535 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157761312 | TGGCATTAGTTTCAT[A/C]GAATCACTTATTTTG | 51429 |
| rs374418898 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157895973 | CTGCTTTAACCCTTA[A/C]GAAAAAGTAACCTGA | 51429 |
| rs374430702 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157934895 | AATCGTAAGGTCCAC[C/G]TCCCACCACAGTGAA | 51429 |
| rs374431717 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157854084 | CCTTGTAAATACACA[C/G]ACTGGTGAGGGTGTG | 51429 |
| rs374484663 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157908305 | CCTTGAATCTCTGAA[C/T]GAATCTCTGAGTGAA | 51429 |
| rs374508359 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157834936 | TACCCGTTAGGTTAC[C/T]GAGATCTGTGGTTAC | 51429 |
| rs374516699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157718308 | CAACCAGTAGTAGGA[C/T]TGCCAGATCCAAGGG | 51429 |
| rs374518124 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157878430 | ATATGGAAGCCCACC[-/T]ATTTTTTTTTTTTTT | 51429 |
| rs374534067 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157747181 | CGAGACTGAGGACCC[C/T]TGCTCAAAGACAAAG | 51429 |
| rs374535321 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157926649 | TAGCCAGGCATGGTG[A/G]CATGCGCCTAAAGTC | 51429 |
| rs374554002 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157930450 | GTTGTTCTCTAAAGC[A/G]GAGGCCCCCAATCCC | 51429 |
| rs374557932 | snp | A/T | 0.000193981 | 0.00984647 | intron-variant | SNX9 | GRCh38.p7 | 6:157873050 | CAAAATTTCTCCAGG[A/T]AATCTCAACTGTAAT | 51429 |
| rs374592252 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157772859 | CCACTAGAGCGTGGA[A/G]CTTAGGAAATAATCT | 51429 |
| rs374625139 | in-del | -/CA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157744742 | CTTTCTTTCTTTCTT[-/CA]TTTTTTTTTTTTTTT | 51429 |
| rs374691306 | snp | C/G | 3.30207e-05 | 0.00406316 | intron-variant | SNX9 | GRCh38.p7 | 6:157937538 | GGTAACCTGATCGTA[C/G]ACATTTATAGAAGAC | 51429 |
| rs374692242 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157737607 | TCAAAAAACCGGCTC[C/T]TGAGTTCATTGATTT | 51429 |
| rs374698445 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157754088 | CCATCAAGTGCAGGG[G/T]CTGCAAATATATCTC | 51429 |
| rs374709747 | snp | A/C/G | | | utr-variant-5-prime | SNX9 | GRCh38.p7 | 6:157766521 | CCCAGTCCTGCTTCT[A/C/G]CTGGACACTTCTCAG | 51429 |
| rs374716582 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157799838 | CACAACACTGGGGAA[A/T]TCTGGGAGATCCAAT | 51429 |
| rs374729654 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157722622 | GGATAGGCAGGAGGC[A/G]GATGAATCGGAGCTC | 51429 |
| rs374736892 | in-del | -/AGT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157841638 | TGCCAGGAGGAAGTT[-/AGT]GTCTAAGGCAGGTAT | 51429 |
| rs374744867 | snp | C/T | 0.00028041 | 0.0118375 | missense | SNX9 | GRCh38.p7 | 6:157875154 | CTCAGGCCAGTTCGT[C/T]GGCTGCCAGCAACAA | 51429 |
| rs374748687 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157765422 | GTGCAGTGGCGCGAT[C/G]TCGGCTCACTGCAAG | 51429 |
| rs374748838 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157777762 | CTTGAAAGGCACTGC[G/T]GCTGCACCTGCAGTG | 51429 |
| rs374763863 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157916706 | GGCTTTTCTTCTGCT[A/G]TTAATACAGCAAATC | 51429 |
| rs374764274 | snp | A/G | 1.66352e-05 | 0.00288398 | intron-variant | SNX9 | GRCh38.p7 | 6:157927085 | CTGTGCTCTCCACTT[A/G]AACCTTACAACATTC | 51429 |
| rs374786354 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157796876 | AGAATAAAATATAAC[C/G]CCAAAGGACAGAGAT | 51429 |
| rs374808418 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157939859 | GGAATCTGTGCAGCC[A/G]CTGGCTTTCTCAGCC | 51429 |
| rs374808723 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157923270 | TGTAGAACTACATAG[A/C]AACTATGATTCTGTG | 51429 |
| rs374828114 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SNX9 | GRCh38.p7 | 6:157740760 | GCCAGGAGCCTCTCC[C/T]GCACCGGCTCAGGGC | 51429 |
| rs374830602 | snp | A/T | 9.88598e-05 | 0.00702995 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157909787 | ATATCAGCTAACACC[A/T]ACTGTAAGTATCCAC | 51429 |
| rs374836897 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157769504 | TTGTGCTGAAGTCAA[C/G]ACCTGAAGGCTGAGT | 51429 |
| rs374839439 | in-del | -/GTTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157852589 | CTACTTTTTTGTTTT[-/GTTT]TTTTGAGACAGGGTC | 51429 |
| rs374842203 | snp | C/T | 3.30923e-05 | 0.00406756 | missense | SNX9 | GRCh38.p7 | 6:157906154 | TTGCGAAACCTGGCA[C/T]GGAACAGTATTTGTT | 51429 |
| rs374845099 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157743885 | AGCCAGGCTTGGTGA[C/T]GTATACCTATAGTCC | 51429 |
| rs374869341 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157929528 | CTTAACCTCTAGAGA[A/G]CAGGGCCTTCTAATC | 51429 |
| rs374898369 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157759074 | GTGCCCTCAGAGAAG[G/T]TTTAAAATCATAGCA | 51429 |
| rs374941427 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157937086 | TATTTTTATATTCTC[C/T]GCTCATATTTAGAAG | 51429 |
| rs374950891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157731415 | AGGAAGGAAATATTT[A/G]GTTTCTTTTCCTAAG | 51429 |
| rs374956146 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157739106 | ACAAATGGGATCTAA[C/G]TAAACTAAAGAGCTT | 51429 |
| rs374968255 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157754298 | ATAAACTAAGTTTCT[C/T]CCAAAGTTAGTTCAG | 51429 |
| rs375007581 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157938128 | GCAGCTTTTCTAGCC[A/G]CTTCCATCTGAGTCT | 51429 |
| rs375012905 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157869763 | GGCCCCATCAGACCT[C/T]GCCAGCCTTTCCCTG | 51429 |
| rs375033989 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157879139 | TACAATGCATATCTC[C/T]AAGGCCCAGCGGTTC | 51429 |
| rs375036858 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157789193 | AGCGAGACTCCGTCT[A/C]AAAAAAAAAAAAAAA | 51429 |
| rs375064001 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157883402 | TTAAGAAACTTCAGA[A/G]TCTCCTCTATTGCCT | 51429 |
| rs375075628 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157862583 | TTCCCTAAGATGTAA[C/T]TGTGATTTATATGCA | 51429 |
| rs375076415 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157938830 | TAGAGAGAAATCCAG[A/G]TGTGAGCAGCAGTTA | 51429 |
| rs375095397 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157728920 | GCCCGGCCAACATGG[C/T]GAAACCCCATGTCTA | 51429 |
| rs375100307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157861582 | ATAACTATAATATTC[C/T]GTATTTAGTTCACAT | 51429 |
| rs375131902 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157824511 | GGTTGCTAGAAACGT[A/T]ATTTTTTATTTTTCG | 51429 |
| rs375204201 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157772853 | TGGAGGCCACTAGAG[C/G]GTGGAGCTTAGGAAA | 51429 |
| rs375233464 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157836609 | TTTCTTTTTTTTTTT[C/T]TGATACAGAGTCTTA | 51429 |
| rs375236568 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157758229 | AAGGAAAGAGAAAGA[A/C/G]AGAAAGAAAGAAAGA | 51429 |
| rs375301456 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157898149 | ATTTCTTACCTCACA[A/G]TACCACTCTGGGTCA | 51429 |
| rs375316788 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157813342 | CAGCACTCACAGCAT[A/G]AACTAACCCTTGGTA | 51429 |
| rs375328940 | in-del | -/GA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157774282 | GGGTAGTGGAGGAGG[-/GA]TGTGGGAGGGAAGGT | 51429 |
| rs375336468 | snp | C/T | 1.67349e-05 | 0.0028926 | intron-variant | SNX9 | GRCh38.p7 | 6:157867509 | TTACTACTCTGTTTG[C/T]GTTTGTAACATCCTC | 51429 |
| rs375355745 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157884604 | CACTCCCACCCCCCC[-/C]GTATGAATTCTTTTT | 51429 |
| rs375361807 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157804831 | TTGAATCCAGGATGT[A/G]AGCTGGAGCGTGGAG | 51429 |
| rs375371233 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840076 | GGTGTCTTTGGATCT[C/T]GGGAAAGAGCAGACC | 51429 |
| rs375385522 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157872768 | TTCCAGGCCTGGGAT[A/G]CGCATCCCACCGCTT | 51429 |
| rs375390859 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157720803 | CTTACTGCCAAACCA[A/G]TCTGTTTGGGGTTGT | 51429 |
| rs375398937 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157780743 | TCTTTCTTTCTCTCT[C/T]TCTCTCTTTCCTTCC | 51429 |
| rs375429157 | in-del | -/TCTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840505 | TTCTTTCTCTTTCTT[-/TCTT]CTTTCTTTTTTAAAG | 51429 |
| rs375444551 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157900556 | TCCTGCAGTGCCAAC[A/G]ATGCACTGGATATAC | 51429 |
| rs375450063 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157882119 | TGCGGCTGGTAACTT[G/T]ATGTTGAAACCAGTG | 51429 |
| rs375451764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157920265 | CCTCTCTGGTCTCCA[A/G]TGTGTATGCATACAG | 51429 |
| rs375453820 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157861980 | AGGTGGGCAGTGTCT[A/G]TGGTGTAGAGATGCT | 51429 |
| rs375461845 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157739954 | GGCCCTGTCGGGCGG[C/T]GGGAGCCTAGGGGAG | 51429 |
| rs375462120 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157883247 | ATACATAATGCTCTC[A/G]CACACTTATACGGTA | 51429 |
| rs375486232 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157818709 | AGGCTGGGACTTCAT[C/T]TGGGAAGCCAACTGG | 51429 |
| rs375516293 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157762118 | TGTGGGGCCGGGAGG[A/G]GCAGAGTACAAGCTC | 51429 |
| rs375563650 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157744016 | AGAGAGACTCTGTCT[A/T]AAAAAAAAAAAAAAG | 51429 |
| rs375563667 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157939682 | GAGCCAGGCCACTAC[A/G]GCAAAAACGAGGAAC | 51429 |
| rs375567258 | snp | G/T | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157891942 | ACGAGGCAAAGTTGA[G/T]ACCTGTGCTGAAGAA | 51429 |
| rs375570616 | snp | A/G | 1.80065e-05 | 0.00300049 | intron-variant | SNX9 | GRCh38.p7 | 6:157936043 | CGTGGCAGAACAGGT[A/G]CTAACATAATCACAC | 51429 |
| rs375645539 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157725264 | GGTTGTGATGTGTCT[C/T]GTGGTTTTCTTCATG | 51429 |
| rs375646282 | snp | A/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890048 | TGGGATTCAAACCCA[A/G]ATAGCAGGCTTTGAG | 51429 |
| rs375660613 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157935682 | GGTGTCATAATGGTA[C/G]TGCCTCATGTTTTAG | 51429 |
| rs375672243 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157898530 | AGCCAGAAACGTGTA[C/T]GTGGATGGGATGTGG | 51429 |
| rs375685168 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157856300 | GAGTATAATAAAGCT[A/G]TTTGTAACCATTATC | 51429 |
| rs375700078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157806102 | AATTAATAAAAGTAC[A/G]GTTATATCTTTCATC | 51429 |
| rs375782524 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157781338 | GACCACCTGCTCTGT[G/T]AGGACATTTGCTCTG | 51429 |
| rs375786363 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157833254 | TCTCAAGATTTTAAG[A/T]AATGAATATTTGCTG | 51429 |
| rs375792081 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157865501 | CCATGATCTCCACTC[A/G]GGTCCCAGCCTCCAA | 51429 |
| rs375872658 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157871527 | ACACCAGGGCCTGTC[A/G]TCGGGTGGGAGGAGG | 51429 |
| rs375877508 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157730261 | AGGCGCGGTGGCTCA[G/T]GCCTGTAATCCCAGC | 51429 |
| rs375899801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157758006 | GGACCTCGTCTCCAC[A/G]AAAAGAAATTAAAAA | 51429 |
| rs375904612 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157810033 | TAGTAACATTATTCA[C/T]TATAACCCTTAACTG | 51429 |
| rs375932188 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157900549 | CTTCTGGTCCTGCAG[G/T]GCCAACAATGCACTG | 51429 |
| rs375939958 | in-del | -/GGCTTGA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157834108 | GACACCAGGGCTTGA[-/GGCTTGA]TCTGATCGGATTTTG | 51429 |
| rs375968885 | in-del | -/TTTG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157907279 | CCTCAGTTTTGTTTT[-/TTTG]TTTGTTTGTTTGTTT | 51429 |
| rs376003492 | in-del | -/GTCT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157911108 | ACAGAGCGAGACTCT[-/GTCT]CAAATAAATAAATAA | 51429 |
| rs376035257 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157849501 | TCAAAAGGTCCTTGG[C/T]GCTGCAGGCGGAAGA | 51429 |
| rs376059824 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157816561 | GAAATGAAATACAGT[A/G]GGGTAAAAGATAGAG | 51429 |
| rs376060854 | in-del | -/TTTG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157759849 | GCCATCAAAGTTTGT[-/TTTG]TTTTTTTGTTTGTTT | 51429 |
| rs376062475 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | SNX9 | GRCh38.p7 | 6:157932133 | AATCACTTTTAGGAA[A/G]TAGTTTAATCCCATT | 51429 |
| rs376075671 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157845710 | TGGTGAATCTGGTAA[A/G]TTGATTGTGTAGCAT | 51429 |
| rs376093578 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157805634 | AGGACACAAATAAAA[-/A]GTTGGAAACTATAGA | 51429 |
| rs376095792 | snp | G/T | 0.000345949 | 0.0131474 | intron-variant | SNX9 | GRCh38.p7 | 6:157909904 | TCTTTCCCTTATTTT[G/T]TAGAACACTAATCGA | 51429 |
| rs376116020 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157746516 | AACATTAAGTATCAA[C/G]GGGCCGTATTTCTGC | 51429 |
| rs376116327 | in-del | -/AC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157869859 | CATACCCCCACACAC[-/AC]TCGCACACACCCTTA | 51429 |
| rs376127275 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157933441 | GTCGGTTTCTGAATA[C/T]TTTAATAATAAACTA | 51429 |
| rs376133192 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157772695 | TGTTATGGCAGCCCA[C/G]GAAACTAGTCCAGGG | 51429 |
| rs376133749 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157830105 | TAGTTATATCTTTTT[C/T]ACCACAAATTGAACA | 51429 |
| rs376141488 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157872638 | ATTAATTCGTATAGC[A/G]ACTTGGGTGCCAGAA | 51429 |
| rs376142364 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157783822 | GCTAATTTTTGTATT[C/T]TTTGTAGAGAAAGGG | 51429 |
| rs376160469 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157801911 | CTTTTTAAAAGATCC[C/T]TGCGGGAAGAGTTGA | 51429 |
| rs376165222 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157766359 | CCTATTGCTGGACTC[A/T]AAATGTGTAACTTGG | 51429 |
| rs376191609 | snp | C/G | 0.000153988 | 0.00877328 | missense | SNX9 | GRCh38.p7 | 6:157875105 | AATTCAGTGGCTGAC[C/G]AAGCCTTCCTTGATT | 51429 |
| rs376201864 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157830823 | TCTCCATTCTTTCTT[G/T]CTGGAACTCTAGTAA | 51429 |
| rs376205037 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157796349 | GACAGGCCAGGTTAC[A/G]ACGTACAAGTTAACC | 51429 |
| rs376216767 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157828003 | TTAAGACTTGTTTAT[G/T]CCATGCATAGATTAG | 51429 |
| rs376227112 | snp | C/T | 1.65162e-05 | 0.00287365 | missense | SNX9 | GRCh38.p7 | 6:157921629 | TCAGAAAGTGAAGTT[C/T]TCCAGCAGTTCCTAA | 51429 |
| rs376262890 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157903258 | ATCTGTGTCTGGAAA[A/G]ATTAAAAACATAACA | 51429 |
| rs376281105 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157869348 | CCAGCCTCAGAGGAG[A/G]CCAGACACCTTCACC | 51429 |
| rs376283716 | in-del | -/AG | 0.000884343 | 0.0210093 | intron-variant | SNX9 | GRCh38.p7 | 6:157875224 | GGCTTTACGGAAAAC[-/AG]AGCGTATTTGTGAAG | 51429 |
| rs376321155 | snp | A/G | | | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157715905 | CTCATGACGAAATTG[A/G]TCAGCCCTGGAATCC | 51429 |
| rs376339728 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157747198 | GCTCAAAGACAAAGA[A/G]TAAAAACCCACCTAC | 51429 |
| rs376344468 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157800603 | GTCAAGACTGCAGGG[A/T]GCTGTGACTGCATCA | 51429 |
| rs376346694 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157814495 | TTGCAAGCAACAACT[A/G]TCTGTGAAAAAAACA | 51429 |
| rs376349790 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157787461 | CCTCTCTCTGTGTAT[A/G]TGTGTGTGTGTGTGT | 51429 |
| rs376350632 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157834504 | GCTGTGTGCCACCCC[C/G]CCGGCCAATTTTTTA | 51429 |
| rs376351219 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157902447 | TGCAGAGAGGTTTGT[A/G]TCATTCGCATGTAGC | 51429 |
| rs376367232 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157864294 | GAGGACAAAGCCTCC[A/G]TGACCTAAACGCCCC | 51429 |
| rs376460895 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | SNX9, LOC107986663 | GRCh38.p7 | 6:157714675 | GCAGAGGAGAGAAAC[A/G]GCACAGATGCCACAC | 51429 |
| rs376473160 | snp | A/G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157751091 | ACTGCTGATAAAGAC[A/G/T]TACCCAAGACTGGGA | 51429 |
| rs376543641 | snp | C/T | 3.2963e-05 | 0.00405961 | intron-variant | SNX9 | GRCh38.p7 | 6:157909656 | CTTCTTTCTGGAACA[C/T]TGGCATAGGTTGGAG | 51429 |
| rs376545567 | in-del | -/CAGT | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157840568 | AACTGCAGGAGTTAA[-/CAGT]CAGTTTGCTTTGATA | 51429 |
| rs376563318 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157825786 | TTTTAATTGTTCCCA[A/G]AGAGTCAAGTTGGTG | 51429 |
| rs376566757 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157901785 | ACCCTTTTCTCCATC[-/A]AAAAAAAATTGATTT | 51429 |
| rs376580452 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SNX9 | GRCh38.p7 | 6:157724158 | ACTCAGGAAAGTACT[C/T]TACTTACTATTACCA | 51429 |
| rs376582857 | in-del | -/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886864 | TCATAATGTGTTTTG[-/T]TTTTTTTTTTCTTTG | 51429 |
| rs376601543 | snp | A/G | 0.00021368 | 0.0103341 | intron-variant | SNX9 | GRCh38.p7 | 6:157928734 | CAGTGCACTGGGCTC[A/G]TAGGGGGTGATGCAG | 51429 |
| rs376604576 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157771977 | GTTCTGGGATTACCG[A/G]CGTGAGGCACTGCAC | 51429 |
| rs376626821 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157841639 | TGCCAGGAGGAAGTT[A/G]TCTAAGGCAGGTATC | 51429 |
| rs376673240 | snp | C/T | 4.94539e-05 | 0.00497238 | missense | SNX9 | GRCh38.p7 | 6:157927154 | AGAGAGATGAGCTGG[C/T]GGGAGTCATGATATT | 51429 |
| rs376685189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157937580 | AAGGAGGCAGATGTG[C/T]GCAGTAGTCAGTATT | 51429 |
| rs376693806 | snp | A/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893606 | TTTTTAACTAGCACC[A/G]TTTGTGTGTGTGTGT | 51429 |
| rs376709833 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157722082 | GGTTTCCAAGGCTCT[C/G]CTGCAAGGGGAACTG | 51429 |
| rs376717053 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157827467 | ATATAATATATAAAC[A/T]TATAGTTTATATAAT | 51429 |
| rs376720943 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157867204 | GCAATCCTCCTGCTA[C/T]TTAGTCTCCCAAGTA | 51429 |
| rs376745846 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157851244 | GCTTGGGTGACAGAG[A/C]AAGATGGTCTCAAAA | 51429 |
| rs376753554 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157866631 | TAAAATCATGGCTGT[G/T]TAGGTAACTCGACCA | 51429 |
| rs376753765 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157749804 | GGCATAAGCCACCAC[A/C]CCCAGCCACTAACTC | 51429 |
| rs376762880 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157770177 | AGATTTTTTGTGGAT[A/C]CCATCAGGCAGGACA | 51429 |
| rs376826244 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157751469 | GGAATTTAGTCTTTA[C/T]CCAAAAAAATTAAAA | 51429 |
| rs376840517 | in-del | -/CAA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157819815 | TCCTGTGGCATGATT[-/CAA]AAAAAAAAAAAAAAA | 51429 |
| rs376856827 | in-del | -/A | 0.0134861 | 0.0810011 | intron-variant | SNX9 | GRCh38.p7 | 6:157777224 | TCTACTAAAAAATAC[-/A]AAAAAATTAGCCAGG | 51429 |
| rs376869928 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157792209 | TGCAGTGGTGCCATC[G/T]AAGCTCACTGCAACC | 51429 |
| rs376872958 | in-del | -/C | | | frameshift-variant | SNX9 | GRCh38.p7 | 6:157901941 | GACTGGGATGGGCCC[-/C]AAATCCTCTTCCTAC | 51429 |
| rs376902612 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157774778 | ATCTTCTGAAATGTG[C/T]TCCACCCTCCCCGAT | 51429 |
| rs376903232 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821181 | TATGAAATTGTTCTG[A/G]TGGGAAAAGCTTGAA | 51429 |
| rs376943665 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157733166 | GGCAGAGCCCAGGCT[A/G]CAACACTGGCTTACA | 51429 |
| rs376947058 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157873037 | CAATTCCTCCACACA[A/G]AATTTCTCCAGGAAA | 51429 |
| rs376961154 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157768113 | ACCCCAGTCTGACCT[A/G]TCTCATGTTCCTCTG | 51429 |
| rs376967743 | in-del | -/GTC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157843870 | AATTATTTCCCATTT[-/GTC]TTTTTTTTTTTTTTT | 51429 |
| rs376974558 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157797566 | TGATACCCATTCACA[A/G]TGTGCACACCTAGAG | 51429 |
| rs377003870 | snp | C/T | 0.000300551 | 0.012255 | intron-variant | SNX9 | GRCh38.p7 | 6:157875031 | CTATGAAAATAATTG[C/T]GGCTCTTTCTCCTAT | 51429 |
| rs377006485 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157932026 | GTCAATTAAAATAAT[C/T]GAAAGAAATCAATTG | 51429 |
| rs377016367 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157759101 | AGCAAGGAACAATGA[C/T]GGTGTTGAGAGTTTC | 51429 |
| rs377016493 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157867927 | CTTCTTCGATATGTT[G/T]ATCTTACAATTTTTT | 51429 |
| rs377018737 | in-del | -/TA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157903269 | GAAAAATTAAAAACA[-/TA]ACATTTGACATATAT | 51429 |
| rs377019068 | snp | A/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894076 | CAGCTGGATCCCTGT[A/G]TCATTTCTTTTTCTT | 51429 |
| rs377019127 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157811565 | CAAAGATAAGATAGG[C/G]AGTCAGTGTGGGCTA | 51429 |
| rs377021904 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157870493 | CTGCAGATAGTCTCA[C/T]CTGCTCTCACACATA | 51429 |
| rs377024986 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157749323 | CTAGTCTGAGACCTT[A/G]GGAAAATTATTTACC | 51429 |
| rs377053049 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157824343 | TCACGGAAGGGAGGA[C/G]CTGGGGGAGGAGGCT | 51429 |
| rs377086659 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | SNX9 | GRCh38.p7 | 6:157750031 | CCCATGTCCATGGAT[C/T]GAAAGAGTTACCATT | 51429 |
| rs377133269 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157926504 | TGCATAGGGTGGGCC[A/G]AGCACAGTGGCTTAT | 51429 |
| rs377141295 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157867042 | TAACTTTGACCTCCT[A/G]GGCTCAAGCAATCCT | 51429 |
| rs377144841 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157845439 | CTGTTGTCTCACTTA[C/T]ACTTATTTTGACAGT | 51429 |
| rs377150736 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157765601 | ACCTCGTGATCCGCC[C/T]GCCTCGGCCTCCCAA | 51429 |
| rs377151949 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157778139 | CGCTACGGGAGGGTC[A/C]CTTCTTGCCTCATCC | 51429 |
| rs377154559 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157798812 | TGTATGTTGTATGTA[C/T]TTTACAATAATGTTT | 51429 |
| rs377186806 | in-del | -/GTAAA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157795025 | GAATTTTAAAATAAA[-/GTAAA]CTGATCAACAGAGAC | 51429 |
| rs377187232 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157805635 | GGACACAAATAAAAA[G/T]TTGGAAACTATAGAA | 51429 |
| rs377214313 | in-del | -/TAAAG | 0.0205511 | 0.0992634 | intron-variant | SNX9 | GRCh38.p7 | 6:157795021 | AGATGAATTTTAAAA[-/TAAAG]TAAACTGATCAACAG | 51429 |
| rs377239271 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157719647 | GCTGTGACAGCAGTC[A/G]CGATTAGAGGAGAGA | 51429 |
| rs377243010 | snp | A/G | 0.000228504 | 0.0106864 | intron-variant | SNX9 | GRCh38.p7 | 6:157928585 | ATGTGACTGACGGCC[A/G]CCTTCACCCACAGAG | 51429 |
| rs377245181 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157734748 | ATGTCAGTAGACTTC[A/G]CTGGTTTTTCCCTTT | 51429 |
| rs377257959 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157942377 | TCGTGCTGTCTGCAC[A/G]CTCAGCAGTGACAGC | 51429 |
| rs377258488 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157774261 | GGTGGGGGAGTGGAG[A/G]AGGTGGGGTAGTGGA | 51429 |
| rs377275078 | in-del | -/TTTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157919979 | TTGTTTGTTTGTTTG[-/TTTT]TTTTATATTTGTCTT | 51429 |
| rs377283756 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157744732 | CTTAGTCTTTCTTTC[C/T]TTCTTTCTTCATTTT | 51429 |
| rs377290096 | snp | A/G | 3.29576e-05 | 0.00405928 | missense | SNX9 | GRCh38.p7 | 6:157901909 | CTAGCAACTGGTGAT[A/G]ATGATGACTGGGATG | 51429 |
| rs377317712 | in-del | -/GCCCCA | 0.0130921 | 0.0798413 | intron-variant | SNX9 | GRCh38.p7 | 6:157773299 | CAGCCAGGGTGCTAG[-/GCCCCA]GCTACACTGTGGACA | 51429 |
| rs377335400 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157899996 | CCCAAATATAATGCA[A/G]TATCATTAACTGTAG | 51429 |
| rs377341402 | snp | C/T | 1.6476e-05 | 0.00287014 | missense | SNX9 | GRCh38.p7 | 6:157940915 | CACAGTAACCGGATC[C/T]ATGATTACAACAGTG | 51429 |
| rs377346954 | snp | A/G | 4.94254e-05 | 0.00497094 | missense | SNX9 | GRCh38.p7 | 6:157909767 | GGTCTAAAGAGCTAC[A/G]TCGAATATCAGCTAA | 51429 |
| rs377381059 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157915656 | ATATATATATATATA[C/T]ACACACACACACACA | 51429 |
| rs377392828 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157842601 | TAATTTGGTGGGTAG[G/T]GGCTTGGGAAGTGGG | 51429 |
| rs377396084 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157816571 | ACAGTGGGGTAAAAG[A/G]TAGAGGATATTGAGG | 51429 |
| rs377402525 | snp | A/C | 0.000153988 | 0.00877328 | missense | SNX9 | GRCh38.p7 | 6:157932201 | GTCTTTCAGCATTAC[A/C]CAAGGAATATCAGAA | 51429 |
| rs377414140 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157755356 | TTTCCTAGTGGCCTC[C/T]CTCAGCATCATATGT | 51429 |
| rs377416546 | in-del | -/AA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157801750 | TTAAAAAAAAAAAAA[-/AA]CCCACAAAATATCCA | 51429 |
| rs377444438 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157842855 | GAGGCTACATGACCC[C/G]GAAATTGTAATTTCT | 51429 |
| rs377497930 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157838674 | AAGAGGATCATTTCT[C/G]TAGTTTAGGGAATGG | 51429 |
| rs377573983 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | SNX9 | GRCh38.p7 | 6:157873064 | GAAATCTCAACTGTA[A/G]TCTTTTTCTTTTTTT | 51429 |
| rs377577712 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157726779 | GTCTGGCTTATGGGA[A/G]CAGGTGCTACTCCTG | 51429 |
| rs377580870 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157741365 | AAACAACAACAACAA[-/C]AAAAAAAAAAACAGA | 51429 |
| rs377589127 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157827556 | ATATTATATTATAGT[A/T]TATATAATATATAAA | 51429 |
| rs377604965 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157897664 | AGGAGCCCACCGCCC[A/C]CCGCCACACCCGGCT | 51429 |
| rs377630825 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157741315 | TTGTGCCACTGCACT[A/C]CAGTCTGGGTAACAC | 51429 |
| rs377668426 | snp | C/G/T | 7.74854e-05 | 0.00622395 | intron-variant | SNX9 | GRCh38.p7 | 6:157897025 | GGTGCAAGGTCCCAC[C/G/T]CTGCCCGCCCATGGC | 51429 |
| rs377669331 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157793138 | TTTTTTGAGTAGAGA[C/T]GGGGTTTCACCACGT | 51429 |
| rs377682059 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157880832 | CCCAGATCTCACACA[A/T]CCTATGTGAATCAGG | 51429 |
| rs377724088 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157902847 | TAATTTTTGTATTTT[C/T]AGTAGAGACGAGGTT | 51429 |
| rs377726416 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157884015 | AGGTACTTTACAATG[G/T]AAGGTATTAAAAGAC | 51429 |
| rs377735252 | in-del | -/GTTAA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157862370 | CATGAATGTGCTTAA[-/GTTAA]ACAAGCTTGCCATTT | 51429 |
| rs377752958 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157819968 | TTAACTAATTGTGTT[A/C]TCACCCCTGGAGTAA | 51429 |
| rs377754269 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157839698 | TCTTGCCCAGGGTGA[A/G]GCATAATTTGAGGGT | 51429 |
| rs386707573 | in-del | AA/TAC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157724547 | ATTAACTGCCTCCTT[AA/TAC]TGTCTTGTACCTAAC | 51429 |
| rs386707574 | multinucleotide-polymorphism | GTA/TTG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157761921 | TTCACTGCAGATATG[GTA/TTG]TGCTGAGAAAAGTTC | 51429 |
| rs386707575 | in-del | A/GTG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157787477 | TGTGTGTGTGTGTGT[A/GTG]TATTTGTGTGTATAT | 51429 |
| rs386707576 | in-del | AA/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157801749 | ACTTAAAAAAAAAAA[AA/C]CCCACAAAATATCCA | 51429 |
| rs386707577 | multinucleotide-polymorphism | CA/TG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157801874 | GGCATGTTGTGAAGA[CA/TG]GGAAGCAACATGATG | 51429 |
| rs386707578 | multinucleotide-polymorphism | AC/GT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157818176 | GTCGCACAATAGGCC[AC/GT]CTGCAAGCTGAGGAG | 51429 |
| rs386707579 | in-del | GC/TTGTGT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157828215 | TCTTAAGTAGAGTGT[GC/TTGTGT]AGTATTTGTATAGTC | 51429 |
| rs386707581 | in-del | CCTTTCCTTCCTTTCTTTCCTTTCC/CCTTTCTTTTCTTTCCTTTCTTTCCTTTCC/CTTTCTTTCCTTTCTTTCCTTTCCTTTCTTTCCTTTCC/TCTTTCTTTTCT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840423 | TTTCTTTCTTTCTTT[lengthTooLong]TTCCTTTCTTTCCTT | 51429 |
| rs386707582 | in-del | CCTTTCCTTTCTTTCCTTTCC/TCT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840432 | TTCTTTTCTTTCTTT[CCTTTCCTTTCTTTCCTTTCC/TCT]TTCCTTTCTTTCCTT | 51429 |
| rs386707583 | in-del | CC/TCT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840459 | TTCCTTTCCTTCCTT[CC/TCT]TTCCTTCTCCCTTCT | 51429 |
| rs386707584 | in-del | CTC/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840467 | CTTCCTTCCTTCCTT[CTC/T]CCTTCTCTCTCTCTC | 51429 |
| rs386707585 | in-del | GC/TCTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157858249 | TTTCTTTTTCTTTTT[GC/TCTT]TTTTTTTTTTTGAGA | 51429 |
| rs386707586 | in-del | C/TCTG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157919464 | AGGTGTTTTTTTTCT[C/TCTG]CTACCTTAAATCTTA | 51429 |
| rs397693219 | in-del | -/A | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157819177 | CCTTATAGGAAAAAA[-/A]CCTCTCCTGCTTCTC | 51429 |
| rs397718776 | in-del | -/CA | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157813101 | TACTGTTAGTGATCA[-/CA]GTGATCTGTGTGCAA | 51429 |
| rs397724921 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157939435 | AGGGAGTAAAAAAAA[-/A]TCAATCCTCAAGGGA | 51429 |
| rs397735340 | in-del | -/A | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157912429 | TTGTTTAAAAAAAAA[-/A]TAAGTTCGGCATGCA | 51429 |
| rs397736917 | in-del | -/GT | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893633 | TGTGTGTGTGTGTGT[-/GT]ATAAGACTCAAATAA | 51429 |
| rs397786482 | in-del | -/T | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157844611 | TTTGTTTTTTTTTTT[-/T]GAGACAGAGTCTCAC | 51429 |
| rs397787886 | in-del | -/T | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157745257 | CCTTTTTTTTTTTTT[-/T]GCTACGTTATTGTGA | 51429 |
| rs397793003 | in-del | -/T | 0 | 0 | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157715697 | TAGGCTTTATCTTGA[-/T]TTTTTTTTTCTTTTT | 51429 |
| rs397797604 | in-del | -/C | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157919906 | GTTAAGTAACTTGCC[-/C]TAAGATTAAATCTCT | 51429 |
| rs397821849 | in-del | -/G | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157877289 | AAAAAGCGGGGGGGG[-/G]CATCTAGTCTAACAT | 51429 |
| rs397825946 | in-del | -/A | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157729561 | GTAGAATATAAAAAA[-/A]GATAGAATTTCTGAC | 51429 |
| rs397841389 | in-del | -/AAATAAAT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157911137 | aataaataaataaat[-/AAATAAAT]GTTGTGAAGAAACAG | 51429 |
| rs397841571 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157898552 | GGGATGTGGCTCATC[-/C]TGCTGGTTTAAGACC | 51429 |
| rs397841572 | in-del | -/AC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157908750 | GCTCAAAACTTACAC[-/AC]GAGGTCTCTACACCC | 51429 |
| rs397885191 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157903766 | TTGCTTATAACCTTA[-/A]GGCAAGTTTCGTGAC | 51429 |
| rs397886105 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157901868 | TCTTTTTTTTTTTTT[-/T]AACTGATGATCTTCC | 51429 |
| rs397887185 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157937625 | ATTATTAAAAAAGAA[-/A]CTCTATAATTCCCAT | 51429 |
| rs397887403 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157738474 | CCCTGCTTTTTTTTT[-/T]CTTTCCATTTGCTTG | 51429 |
| rs397887611 | in-del | -/GA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157934324 | GGAAGGAGAGAGAGA[-/GA]TGGAAGGTAAACTGA | 51429 |
| rs397887697 | in-del | -/TGA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157897195 | GTCCTACAGTCATGA[-/TGA]CACTGTCTACCTGGA | 51429 |
| rs397887781 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157784383 | TTTTTTTTTTTTTTT[-/T]AGATGGCGTCTCACT | 51429 |
| rs397887803 | in-del | -/TG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157781842 | GTGTGTGTGTGTGTG[-/TG]CATATGTGCAGTGTA | 51429 |
| rs397888156 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157853803 | GTTTAAAAAAAAAAA[-/A]CAACAAAGGTGGTGA | 51429 |
| rs397888230 | in-del | -/TT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157723323 | CACCTCTAAACTCTT[-/TT]AAAAGTAGACAGGGC | 51429 |
| rs397888348 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157732720 | TGTTTTGTTTTGTTT[-/T]GTTTGTTTTTAGAGA | 51429 |
| rs397956813 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157743426 | GCAAAAAAAAAAAAA[-/A]CAAAAACAAAAACGG | 51429 |
| rs397963172 | in-del | -/AGA | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157892050 | GATGGACAGTTAAGA[-/AGA]GCTTTGCAAAATAAG | 51429 |
| rs397969480 | in-del | -/AA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157777393 | AAAAAAAAAAAAAAA[-/AA]GGCAAAAGCAGTCAG | 51429 |
| rs398003177 | in-del | -/T | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157729117 | TTTTTTAATTTTTAA[-/T]TTTTTTTTTTTTTTT | 51429 |
| rs398003178 | in-del | -/T | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157741378 | ACATGTGATTCTCTG[-/T]TTTTTTTTTTTTGTT | 51429 |
| rs398003179 | in-del | -/T | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157744030 | ATGTATAATTTTTTC[-/T]TTTTTTTTTTTTTTA | 51429 |
| rs398003180 | in-del | -/T | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157750772 | ATTGCGTTATTAGGG[-/T]TTTTTTTTTTTCTGT | 51429 |
| rs527243919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157836882 | AGGCGTGAGCCACCG[C/T]GCCCGGCCGAGAACA | 51429 |
| rs527253748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157864479 | ACATTCTGCTTCACT[A/G]CATTCTAAGTTTAGT | 51429 |
| rs527255465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157843356 | CTGTTGACTGGAAGC[C/T]TTATAACGCAAACAG | 51429 |
| rs527262421 | snp | C/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887886 | TTCCCTACAGGACAG[C/T]TGTGGAACCGGGATT | 51429 |
| rs527269885 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157730481 | CAGTGAGCTGAGATC[A/G]TGCCACTGCACTCCA | 51429 |
| rs527280313 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157881882 | TAATATAAAAGTGCA[C/T]GGTGAAGCAGCAGGT | 51429 |
| rs527292912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157876848 | TTCTACCTACCAGGT[A/G]CCAGTCACATGCACG | 51429 |
| rs527327394 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157741344 | ACAGCGAGACTCTGT[C/G]TCAAAAAACAACAAC | 51429 |
| rs527330223 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157748594 | ATTAGCAGGGCATGG[G/T]GGTACGCGCCTGTAG | 51429 |
| rs527334026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157936775 | CTTGTCATAGCTACA[C/T]AGCTTTTATTGGAGT | 51429 |
| rs527345676 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157837513 | CCAGTTTTTAATGTT[A/G]TTTGTGTGGTAAGTA | 51429 |
| rs527356666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890685 | AGGGCCCCACGTTCA[C/T]GGGCAGCAGGAGATG | 51429 |
| rs527375316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157801083 | TACCTTTCTTTGGGC[A/G]TATGACTTCAGGTGA | 51429 |
| rs527379506 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157907038 | ATTACTTGTGCCTGC[A/G]TGTTTGAAAAACTCC | 51429 |
| rs527383419 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157842927 | AGACAAGAAGGGGGT[A/C]TTTTCAGGAAAGGGC | 51429 |
| rs527387762 | snp | A/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885826 | GGGATGATCTGTACT[A/G]ACCTGAAGTGGACGT | 51429 |
| rs527394179 | in-del | -/T | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157767943 | CAGAGTGGAGGCTCC[-/T]TGGGGGGACAGCTGG | 51429 |
| rs527403601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157755153 | CAACCTGCTTTATCA[A/G]CAAGGTCTTTATGAC | 51429 |
| rs527413156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157793360 | ACCCAAGGACCTTGG[C/T]TTTGGAGACATTCAT | 51429 |
| rs527434711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157891192 | TCCTGCCACCACACC[C/T]GGCTTTTTGTATTTT | 51429 |
| rs527446131 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157910522 | GCTGCCAGGTTTTCT[A/G]CTTATTTTGATTATT | 51429 |
| rs527448393 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157917481 | AAGTCTACCTTATTG[A/C]GTTTTCATGTTCATT | 51429 |
| rs527449753 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157737008 | GATGAAGCTAACTTG[A/G]TGATGGTGGATAAGC | 51429 |
| rs527454714 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | SNX9 | GRCh38.p7 | 6:157823818 | GGCGACTGGCGCTCT[G/T]TGGCGTCCGGCGTCC | 51429 |
| rs527458050 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157940225 | GCCTGCTAGGTCCAG[C/T]GCAGACACACCAGAG | 51429 |
| rs527465769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157772757 | TGAGGTTAAGAAAGT[A/G]TGAGGTTAAGAAAAC | 51429 |
| rs527474390 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157865352 | CAGGAAAAAAAAAAA[A/C]AAAAAAACACCACAT | 51429 |
| rs527491147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157817111 | TGCTGGTGCCTTGAT[A/G]TTGGACTTTTCAGCC | 51429 |
| rs527503154 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157796427 | TGTTGGTCAGCAAGG[-/C]AGTGGGGGAAGAGAG | 51429 |
| rs527508719 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157903662 | AGTGGCCACGTTTTC[A/C]TGGCTGATGAGTGAG | 51429 |
| rs527526664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157730021 | GAATGGGTGTGGGGG[C/T]GGGGAGTTGGGGCTG | 51429 |
| rs527537992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157778006 | CTATTACTGCCATAA[C/T]AAATAACAGCAAACC | 51429 |
| rs527545236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157877704 | TTTTGAGAGCGGGAA[C/T]CTCAGAGAAGCTGGG | 51429 |
| rs527546873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157787142 | CCTCCCCTGAGTAAG[A/G]GAATTCCTTCTGCCT | 51429 |
| rs527571196 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157830574 | GAGGACAGGTGCTAC[A/G]TTAGTTCTAGAACAG | 51429 |
| rs527573706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157741850 | AATTACTAAAGCATC[A/G]CATTTCCGGCGGAGA | 51429 |
| rs527585039 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157916648 | CATGAATAGATGCTG[C/G]ATTTTGTCCCATGTA | 51429 |
| rs527630463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157898598 | TTAACTTCCTGTTTG[A/G]CTAGGCTATGAATAG | 51429 |
| rs527634830 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157778820 | GCACAGGCTCCTAGG[G/T]GGAAACAGGGAGCAA | 51429 |
| rs527666067 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157851540 | CCCCCATTCTACTTT[C/T]TGGCTTCATTTGCCT | 51429 |
| rs527675791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157938330 | TGATTTCCATTACGT[A/G]CTACTCCTCAAATGG | 51429 |
| rs527700068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157802572 | TCCCCATTGAGACCC[A/G]GTAATAACATTTTTA | 51429 |
| rs527713690 | snp | A/T | 0.00478085 | 0.0486577 | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157715647 | GTGTGTGTTTTTGTT[A/T]TTCTCTTTTATAAAG | 51429 |
| rs527719512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157911290 | AGGCCTGTAAGAGAT[A/G]TAAAAGAGACACTGA | 51429 |
| rs527721941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157756494 | TCTACATAAGTATGA[C/T]TCCCTGTCTTTATAA | 51429 |
| rs527739409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157722316 | TTGTTATCCTCATCT[A/G]ACAATAAGCCCTCTA | 51429 |
| rs527740030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157858272 | TTTTTTTGAGATGGA[A/G]TTTTGCTCTTGTTGC | 51429 |
| rs527740433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157865810 | TCATTAAGCAAATAC[A/G]TAGAAAGGGCAATGG | 51429 |
| rs527742161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157918529 | ATAGGCAAGATAGTT[A/G]GATCTTACTTTTTTA | 51429 |
| rs527750889 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157767825 | GAAAGTATGGCTTGG[G/T]TTCCCAATGTCAGGC | 51429 |
| rs527768759 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157904564 | GGAGTTGTCATGATA[C/T]ATAATCCCCACAGAA | 51429 |
| rs527787348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157768403 | GCACCCTGGGTTTAG[C/T]GCGATGGCTGTTTTG | 51429 |
| rs527800266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157858747 | TCACAATCATGGTGG[A/G]AGGCAAAGGAGAAGC | 51429 |
| rs527802695 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, downstream-variant-500B | SNX9, LOC107986663 | GRCh38.p7 | 6:157714992 | AGGTTGCAGTGAGCC[A/G]AGATTGTGCCACTGC | 51429 |
| rs527803293 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157723297 | TTTCTACACACTTTA[C/G]TATTTTAAGCCACCT | 51429 |
| rs527807109 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157933820 | TCCCCACTGGGAGCT[C/G/T]CTTCGTGATTCTTTA | 51429 |
| rs527815304 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157943393 | GCTCAAGTGCTTACA[C/T]TTCAAGAGGGAGGAC | 51429 |
| rs527816440 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157799577 | GCTGATAAAGACATA[C/T]CCGAGACTGGGAAGA | 51429 |
| rs527825284 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157773313 | GGCCCCAGCTACACT[A/G]TGGACACAGTGGACG | 51429 |
| rs527835343 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157904310 | GCGTGGTGGCACGCC[G/T]GTAATCCTAGCTACT | 51429 |
| rs527841051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157839191 | CTTGTGTATAATTAC[C/T]GTTATATGTGTGTGG | 51429 |
| rs527844695 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157750773 | CAGAAAAAAAAAAAA[A/C]CCTAATAACGCAATT | 51429 |
| rs527848498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157742670 | GTGCAGCGGTTCAGG[A/G]GCTCCTGGCTGATGG | 51429 |
| rs527860073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157925661 | TACACAAGATTTTGA[C/T]TGTAGTTCCTAAGCA | 51429 |
| rs527871611 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157853801 | TGTTTAAAAAAAAAA[-/C]AACAACAAAGGTGGT | 51429 |
| rs527872342 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157735920 | AGTGAGCTAAGATAA[C/T]GCCACTGCACTCTAA | 51429 |
| rs527890610 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157914995 | GGTAGAAGTAGTGCA[-/T]TTTTTTTTCACATCG | 51429 |
| rs527909451 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | SNX9, LOC107986663 | GRCh38.p7 | 6:157714951 | AGGAGGCTGAGGCAG[A/G]AGAATTGCTAGAACC | 51429 |
| rs527927768 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157832271 | ATAAATTAAAGAGGG[A/G]GAAATGCAGCTTCAT | 51429 |
| rs527933924 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157938865 | AGTGAGACCTTTTAA[A/G]CCCCTCGTTTGCAGG | 51429 |
| rs527935326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157743745 | TAAGGCCAGGCATGG[C/T]GGCTCACACCTATAA | 51429 |
| rs527936553 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157795484 | TGAATGTGGATAGGG[G/T]ATCAGATATTGTAAA | 51429 |
| rs527938841 | snp | A/G | 6.69725e-05 | 0.00578634 | intron-variant | SNX9 | GRCh38.p7 | 6:157932164 | TCAGTTTGCTCAGAA[A/G]ACTAATCGTTTATTC | 51429 |
| rs527970866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157802938 | TTTTCACTGCTTTGG[A/G]GTGGAGGAGGTTGGG | 51429 |
| rs527972420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885289 | CTGCTGTGATCTACC[C/T]TCATTTTTAGAAGAA | 51429 |
| rs527985456 | snp | A/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893346 | AGTATTTGACATAGA[A/G]TAAAATAACAAGTAA | 51429 |
| rs528008209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157795847 | CAATGTTGGAACAGC[A/G]TCTGGGGTGGTATAA | 51429 |
| rs528008382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157756917 | GCCCCGGTGCAGAGA[A/G]GACGCCGGGAGAATC | 51429 |
| rs528015027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885884 | GCCCATAAGAGCTGC[A/G]ACCACTCACAGTATG | 51429 |
| rs528016073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157749763 | GTGATCCGCCTGCCT[C/T]AGCTTCCCAAAGTAC | 51429 |
| rs528028357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157826035 | TGAATTTATCAGAGA[C/T]TTGGCTATAGTATCT | 51429 |
| rs528043875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157804862 | GGAGGGAGGAGCCCG[C/T]CTTTACTGCGGTAGG | 51429 |
| rs528088081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157764871 | ACTGAGCTGGAAAAT[C/T]TGCTGGTAGCACGTA | 51429 |
| rs528088565 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157758674 | CTCTGGCTGGGGTCA[C/T]TGGGCACATGGTGAC | 51429 |
| rs528097069 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157803634 | CACTAGAATTATCAG[C/T]GGTTAATGACAAGTA | 51429 |
| rs528104340 | in-del | -/TAT | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157843100 | TAATTTCCTCAATTA[-/TAT]TAATTTTGCAAAGGT | 51429 |
| rs528121344 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157718303 | TATAACAACCAGTAG[A/T]AGGATTGCCAGATCC | 51429 |
| rs528125676 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157945539 | AGTCCCAGGGAGATG[G/T]TCTGTGGGCACCCCC | 51429 |
| rs528125759 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157759335 | GCTGGCCCTGATGGG[C/T]CCAGGAGCACTCATG | 51429 |
| rs528131633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157855479 | GCCTCTTCTGTTAGC[A/G]CGATGTAAGGATACC | 51429 |
| rs528131643 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157847405 | ACTGCGCCCAGCCTT[A/G]TAGTACTTATTTTAA | 51429 |
| rs528139207 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157901177 | CTGGCAGTCCCACCT[A/G]GCACTGTCTTTACAC | 51429 |
| rs528140332 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157868020 | CCCTAGCATGATAAT[A/T]CTGTATCTCTAGAAT | 51429 |
| rs528143846 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157861824 | TAACTAATAATAAAA[A/T]AGAACAGTTATTATA | 51429 |
| rs528148808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157775710 | AATTGCTTCAAACAG[C/T]AGCCACCTTCTGTTT | 51429 |
| rs528150026 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157725728 | AGATTACGGATAGAC[A/G]CAGATAACTTCAGAC | 51429 |
| rs528151770 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157934124 | AATAATGTAAATGGG[C/T]TTGATTCCTGGAAAT | 51429 |
| rs528154591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157812876 | CATTGACATAGAGAT[A/G]GGAAATACACCAATA | 51429 |
| rs528165189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157820486 | TACAAATATATTCTA[C/T]GAAAGTGGGTCTCCT | 51429 |
| rs528184625 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157764161 | ACATAGTCTTCCGTG[A/G]TATTTCCCATGGCTG | 51429 |
| rs528216232 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157726825 | TTAACTAAAATATTT[A/T]AAAACAACACAGGAG | 51429 |
| rs528230316 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157746070 | TAGCATCCAAAACAG[C/G]AATCAGTAAAAAACA | 51429 |
| rs528237484 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157895612 | CCTTGCAGAATGTTT[C/T]ATGCTGTTAAGAGAA | 51429 |
| rs528239450 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157917651 | CCCTGATATAAAATG[G/T]TATAGTATTTGCATA | 51429 |
| rs528251015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157841604 | GTAGGCTGTGTGTAG[C/T]TTTCCCATGGGGAGG | 51429 |
| rs528251582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157928952 | GTTCCAGTAATTTGG[A/G]GCTTTATAATCTTTG | 51429 |
| rs528267597 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157783825 | AATTTTTGTATTTTT[C/T]GTAGAGAAAGGGTTT | 51429 |
| rs528295412 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157783933 | CAGGCGTGAGCCACC[A/G]TGCCCAGCCAATACC | 51429 |
| rs528295465 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157871715 | AAATGCTAGATGTGT[A/G]TAAGTTAAATAGATT | 51429 |
| rs528296893 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157882420 | GCACTTATTCTACAG[A/C/T]CCTTGGATCGAGGAG | 51429 |
| rs528298406 | in-del | -/TG | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157944549 | ACACTTTTTGGACTT[-/TG]TGTGTGATTTTTGTT | 51429 |
| rs528311928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157921789 | CCAGTGACAGTGAGG[A/G]GACAGAAACCTAAAT | 51429 |
| rs528337128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157835563 | GATATGGTTAGGCTT[C/T]GTGTCCCCACCCAAA | 51429 |
| rs528345108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157941316 | TGAGGTCACCCAGCC[A/G]TCCCTGGGACTCCGT | 51429 |
| rs528345430 | snp | C/G/T | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157845392 | CTGGGATTACAGGTG[C/G/T]GAGCCACCGTGCCCG | 51429 |
| rs528361065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157798877 | AATAAAATGGTTGCT[C/T]GGGAAATACATTCAG | 51429 |
| rs528363063 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157806186 | GCTACTCTATAAATT[C/G]TCATCATTTTAAAAA | 51429 |
| rs528372031 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157896107 | TTCTAGATTGTAGGA[A/G]GGAGGCTGCCCAGAT | 51429 |
| rs528375595 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157916074 | GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 51429 |
| rs528378448 | in-del | -/TTA/TTGTTT | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157792946 | TTTCTGTTGTTGTTG[-/TTA/TTGTTT]TTGTTTTTGTTTTTG | 51429 |
| rs528395001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157848178 | TGGCTTTTCACCACT[A/G]TGTCCCCCTAGAACA | 51429 |
| rs528397498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157759891 | GTTTTCTTTTTTAGA[C/T]GGAGTCTTGCTGTGT | 51429 |
| rs528399690 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157841131 | GCAGAATGCTGTTAT[A/G]GGCTAAGAAGAAATG | 51429 |
| rs528404705 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157791671 | AGGCTGTTAAGTCAG[A/T]CCAGAGCAATTGGTA | 51429 |
| rs528405024 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157935534 | AGGTGCAGGGAAAAA[A/G]GGGGCCGAGGGAGAA | 51429 |
| rs528414848 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157781151 | TATTTGGTTGAACTT[A/C]CACCATTCATGTTTT | 51429 |
| rs528416080 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157753054 | ACAGGGTTGGGGGTA[C/G]GGTTACAGATTAACA | 51429 |
| rs528420706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157829076 | TGTTCTTTTAATCAT[A/G]TGTTTTAGTGTATTT | 51429 |
| rs528425800 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889248 | CCAGCCTGGCCAACA[A/T]GGTGAAACCCCATCT | 51429 |
| rs528426591 | in-del | -/TC | 0.240478 | 0.249819 | intron-variant | SNX9 | GRCh38.p7 | 6:157813886 | GGGAAATTGCTATTA[-/TC]TCTCTCTCTCTCTCT | 51429 |
| rs528434559 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157881671 | ATAGCCTTATTGCTG[A/C]TAAGGAGAAGGTTTG | 51429 |
| rs528463510 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157718198 | GGTGATGGGCACTTG[A/G]GTTGATTCCAGGACT | 51429 |
| rs528477263 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157771580 | ACTGGTTTTGATTCT[C/G]AGAAGAGAAGAGGAA | 51429 |
| rs528478400 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893934 | GTACAAATAGATCAC[G/T]AAGAAACAAGAGAGT | 51429 |
| rs528479450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157777243 | AAATTAGCCAGGCGC[A/G]GTGGCGGGTGCCTGT | 51429 |
| rs528485853 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157814856 | TTTATGCAAGAGATC[A/T]GTAGGTCCTTAATCC | 51429 |
| rs528497309 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157926720 | TGGAAGCTCAAGGAT[A/G]CAGTGAGCTGAGATC | 51429 |
| rs528550803 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157828733 | TTCCTCCTCAGCCCC[A/G/T]CAAAGTATTGGGATT | 51429 |
| rs528567930 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157740224 | AAGGCCACATTGCCC[A/G]ACTCCAAGGGGCTCT | 51429 |
| rs528572854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157922317 | ATCATTTTATTCTCT[A/G]AAGATGTTTCCTCCA | 51429 |
| rs528588705 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157858667 | GTAAAGACATACCTG[A/T]GACTGGGTAATTTAT | 51429 |
| rs528619643 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157876276 | GGCCAACATGGTGAA[A/G]CCCCATCTCTACTAA | 51429 |
| rs528624563 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157752043 | TAAAAACACAAAAAT[A/G]AGCTGGGCATGGTGT | 51429 |
| rs528625164 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157785515 | CCAACTATATTAACA[G/T]AATAAAGGATAAAAA | 51429 |
| rs528638404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157857409 | TCCTTTTAATGAAAA[A/G]TGCTGCTCGGAATTC | 51429 |
| rs528642383 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157776736 | TGTGGCTTGGCTCCC[A/G]TAGGTTTGTTTGCTA | 51429 |
| rs528645075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157815932 | ACCTAATGTAGGTGA[C/T]GGGTTGATGGATGCG | 51429 |
| rs528652093 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157807353 | AAATTTGATCATGTT[A/T]CTCTGTCACTTAAAA | 51429 |
| rs528658607 | snp | C/T | 0.000136437 | 0.00825833 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157896976 | CACTGCCTTCGGCCA[C/T]CCCCAGGCCTACCAA | 51429 |
| rs528658722 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157902777 | GGTTCAAGCAATTCT[C/T]GTGCCTCAGCCACCT | 51429 |
| rs528677747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157766911 | GTCTCAGTTTCCTCA[C/T]TGGGTTGTTTTGAAA | 51429 |
| rs528681983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157807933 | AAAATTTACAGTGCC[C/T]TCATTGTGTGAAAAT | 51429 |
| rs528701008 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157849694 | AGAGGTGGAAAGGAA[A/T]GAGAGGAGGAGTCAA | 51429 |
| rs528704319 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157786871 | CTTGCTTTAGTCTAA[C/T]AAATGATCCCCATTC | 51429 |
| rs528705388 | in-del | -/G | 0.207864 | 0.246424 | intron-variant | SNX9 | GRCh38.p7 | 6:157877281 | AAAGAAAAAAAAAGC[-/G]GGGGGGGGCATCTAG | 51429 |
| rs528717352 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157728267 | GATCTCCAGGTACAC[C/G]TGGGATGGAGGTTCA | 51429 |
| rs528720427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157897593 | GCTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA | 51429 |
| rs528760854 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157815436 | TTGCTCAGGCTGGTC[C/T]TGAACTCCTGGACTC | 51429 |
| rs528774374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157856554 | TCCTTTAAGAATTCA[A/G]ATTTCATAATCATTT | 51429 |
| rs528793902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157902163 | TGATCTCCTAAGTTT[C/T]GGATATGATTCAGTT | 51429 |
| rs528796454 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157864528 | TTCTATATTTGGAAA[C/G]TAATTGGATTCAGCT | 51429 |
| rs528810916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157941953 | GATTTGCCTTTCATT[A/G]TATATTAGAATATAA | 51429 |
| rs528832097 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157824899 | TTGTTGCCAGACATT[C/G]CAGAAATTACCAGTT | 51429 |
| rs528842984 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157830852 | AACATGAAAAGGACC[A/C/G]ATGGAAATCTAACTT | 51429 |
| rs528862362 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157737626 | GTTCATTGATTTTTT[G/T]AAGAGTTTTTCGTGT | 51429 |
| rs528870712 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157744400 | TCTTCAATATAATTT[G/T]AAGACATGACTCATG | 51429 |
| rs528873233 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157871898 | TCTCATGCCCCAGCC[G/T]CCCGAGTAGCTGGGA | 51429 |
| rs528883421 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157780498 | TCCAGGACCAGAATT[C/G]TCTCCTTTTCAGCAG | 51429 |
| rs528922107 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157817765 | CTGTAATTCCAGCTA[C/T]TTGGGAGGCTGAGGT | 51429 |
| rs528933494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157788148 | ACTTGTCCAAAGTTA[C/T]ATTGTTAGTAATAAC | 51429 |
| rs528975731 | snp | A/G | | | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157944289 | TGAAATCAAATGAAT[A/G]TGAGAACATCTTGTT | 51429 |
| rs528995334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157917687 | TATGCACATTCTCCC[A/G]TATATTTTAAATCAT | 51429 |
| rs529013797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157871191 | TCAAGACCAGCCTTA[A/G]TAACATGGCAAAACC | 51429 |
| rs529026703 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157878984 | ATTTTAAGATTCTTC[C/T]ATCAAACTAGCAGAG | 51429 |
| rs529030695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157852263 | TGTTTAAAGAAGTAT[A/G]TCTGAATTTTACACA | 51429 |
| rs529036825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157860296 | CCTGTAGTCCTGTCT[A/G]TCAGGAGGCTGAGGC | 51429 |
| rs529044720 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157899224 | TCTCATCTTTTTCTC[A/C]CACACCCCAACTCGG | 51429 |
| rs529047981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157779914 | AAAAGTCTGTCTTCA[A/G]TAGTTTCCTTTGTGC | 51429 |
| rs529057980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157905773 | TGCCCCCTGTGGCCA[A/G]CTCAGATTGGCGTGC | 51429 |
| rs529071613 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157944649 | TATTTCTTCTGACAT[G/T]AATTCATCATTTCAG | 51429 |
| rs529074735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157769765 | CCATGTGGAGAGGCA[A/G]TGGAAGGGGAAGCAC | 51429 |
| rs529078572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157939121 | TTGGGTGTGTCATTT[C/T]AGGCACAATTTTTTT | 51429 |
| rs529088146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157757144 | CGAGAGAGGGAGTCC[A/G]GAAAAGTGGACTAGG | 51429 |
| rs529101439 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157837324 | TAAGTTAGCCAGAAA[A/G]CATGCGATACAGTTT | 51429 |
| rs529101609 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893171 | TAGAAGGAAGGGTTT[C/G]TCTTAGCTGAAGTGT | 51429 |
| rs529106079 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157747100 | AATGCTCACTTGTCC[A/G]CCGCTCACCTCCTGC | 51429 |
| rs529108899 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157716363 | AGGCCAGGGCTGTCT[G/T]AGGTTCTTTTTTCAT | 51429 |
| rs529112319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157897286 | TCACAGAACTCAGGG[A/G]AACACTTTACTTACT | 51429 |
| rs529113810 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157763502 | GCCCTGGGGTTCCGT[C/G]GTTGACCCGGAAGCA | 51429 |
| rs529143939 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157723480 | TGTCACTGTGAACTA[A/G]TAACTTCAGGTCTGT | 51429 |
| rs529158519 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157768468 | GATGAACTGGCACCG[A/T]TGACACCATACTTCA | 51429 |
| rs529189612 | in-del | -/GGGGGC | 0.00835141 | 0.0640778 | intron-variant | SNX9 | GRCh38.p7 | 6:157939957 | GACTCCTCTAGAGTT[-/GGGGGC]AGGGGCAGGGGGGAC | 51429 |
| rs529191345 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157874207 | AGAGAATCCGATGCA[A/G]TCTCTAGGCTTTCCC | 51429 |
| rs529195130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157724407 | TGAGTCCCACAGCAT[A/G]TAGCTGTAACTTCAG | 51429 |
| rs529205621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157751727 | TGCTGCATGATTCTA[C/T]TTAACGGAGGTATCT | 51429 |
| rs529227550 | in-del | -/GGCGGCGGC | 0.138399 | 0.223708 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157823039 | CCAAGGGCGCCCGGG[-/GGCGGCGGC]GGCGGCGGCGGCGGT | 51429 |
| rs529227883 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157849666 | TAGAAAGTAGATTTG[C/T]CAGGCCTTTCTTAGA | 51429 |
| rs529239869 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157814985 | CAAGGCTGGCCCTGG[G/T]GTTGGTGTGCTGGAG | 51429 |
| rs529250321 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157794183 | CTGCTGTTCTCATGA[C/T]AGTGAATAAGTCTCA | 51429 |
| rs529286566 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157789807 | TGGCAGCTTTTACAT[C/G]GCTTAGGATTAAGTC | 51429 |
| rs529313207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157744642 | ATTGAAAAGGCTTGC[A/G]ACAGCCCCCCCAGCA | 51429 |
| rs529331507 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157833288 | TTGTAACAAGGAAAA[A/T]AAAGATTTTTTTTTA | 51429 |
| rs529335245 | in-del | -/AGGGGTG | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157813752 | CTTTCCAGACAGAAA[-/AGGGGTG]AGGAAAGCAGTATCA | 51429 |
| rs529380603 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157796143 | TCTTTTTTTTTTCTT[A/C]ATTATTGTTCCTGTC | 51429 |
| rs529393675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157845674 | ACATGCCACATATTT[C/T]ATACAAAGCATAGAC | 51429 |
| rs529418758 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157726020 | GTGTTCATTCCCTCT[C/G]TTTCCCACGCTCACT | 51429 |
| rs529432003 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157774901 | GAATGCAAGGCCAGT[C/G]GTCACAGTGCAGTGA | 51429 |
| rs529441366 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157772922 | GGTGAGCTGGAGCTG[C/G]ACACGGATAAGGCCA | 51429 |
| rs529452873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157867483 | AAGTGAACTGTACAC[C/T]TTTTGTGTTTTTACT | 51429 |
| rs529461401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157827596 | TATTATAGTTTATAT[A/G]TATATGAGATATATA | 51429 |
| rs529476404 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157753035 | AGCCCATGTTTCTGC[C/G]AGCACAGGGTTGGGG | 51429 |
| rs529482028 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157906581 | AAGTACATGTATGTT[A/T]TCAGAATAAGGTACC | 51429 |
| rs529488805 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157927525 | CCTAAAACCCACTCA[A/G]TATTCAGACAGCAAA | 51429 |
| rs529527695 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157898496 | TCTCAGCAGCTAACA[C/T]GTTTGTTTTAAAATC | 51429 |
| rs529528318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157914065 | TTAAGAAATTGCCCA[A/G]CTGTTTTTCAAAGAA | 51429 |
| rs529542021 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157738525 | TTATTTTGAGCCTAT[A/G]TGTGTCTTTGCACAT | 51429 |
| rs529544583 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157907418 | TCCCGAGTAGCTGGG[A/C]TTACAGGCATGCACC | 51429 |
| rs529547561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157730638 | GACTTATGTCCCTTA[A/G]TTCTTTTTTTTTTTT | 51429 |
| rs529549676 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157828036 | AGAACAATTCAGAAG[C/G/T]CATACTTTGTAGCCC | 51429 |
| rs529570390 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157919979 | TTTGTTTGTTTGTTT[G/T]TTTTATATTTGTCTT | 51429 |
| rs529573244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157873847 | AGCTGTTAGGATGGA[C/T]ACCCAGGAGAGCAAC | 51429 |
| rs529591542 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157774573 | GGCCCCGTCTGCAAC[A/G]GACAGGTCTCTGCAC | 51429 |
| rs529591649 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157782716 | AGATGGTGAAACCCC[A/G]TCTCTACTAAAAAGA | 51429 |
| rs529629246 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | SNX9 | GRCh38.p7 | 6:157826495 | ACAGAGTGAGACTCC[A/G]TCTCAAGAAAAAAAA | 51429 |
| rs529696890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157929440 | CACTGCTGTCCCATG[C/T]GCAGATGCCTTTAAC | 51429 |
| rs529696981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157936592 | GGGGATTCTAAAGAA[C/T]AGGAAAGAATGCTGG | 51429 |
| rs529699745 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157922792 | GTCTTATGAATTTGT[A/G]TATGTTTATGGTGAG | 51429 |
| rs529703426 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157842786 | GATCTTAGGTTTTAC[A/G]ATAGTGATGTTATCC | 51429 |
| rs529715834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157848291 | GTCATTGGCTTTACC[C/T]ACCCAGAGAATGCAG | 51429 |
| rs529740964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157836395 | CAGAAAGATATGGCA[A/G]TGGTAATAAGCTTCC | 51429 |
| rs529755834 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157806004 | TGAAGTAAGTGCCTG[A/T]CGTAGTAATAGGCAC | 51429 |
| rs529764297 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157930155 | TACCTCTGCCTCTTC[C/G]TCTACTAGCAGTAAT | 51429 |
| rs529770782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157753951 | AAGCCAGTAAGCCAG[A/G]AGTACTGGTTGGTCA | 51429 |
| rs529778152 | snp | A/G | 1.64991e-05 | 0.00287215 | missense | SNX9 | GRCh38.p7 | 6:157896842 | GTTGGCAGTGGCAAT[A/G]ACCCCTGGTCAGCCT | 51429 |
| rs529783589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890126 | TCAATTCCAATAGCT[C/T]CCTAAAGGGAGTTAA | 51429 |
| rs529799543 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157777410 | GCAAAAGCAGTCAGT[A/C]AATTCTCAACAAGTA | 51429 |
| rs529803253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157807178 | ACTCTTCCTGCACAG[C/T]TATAGGACAAGGACT | 51429 |
| rs529819252 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157848818 | ATAAGGCCGTCCATG[A/G]GAGGGATAGATACGT | 51429 |
| rs529836272 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157936124 | CTGTCTTAGGACAAA[C/G]GTCCCAAATAAGTAC | 51429 |
| rs529898559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157793240 | CAGGCGTGAGCCCAC[A/G]CACCCAGCCTTAGAA | 51429 |
| rs529901109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157785842 | CCAGCCATTGAACTC[C/T]GAAATTGACTGGAGT | 51429 |
| rs529904570 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157799734 | CCCTGATAAACCCAT[C/G]AGATCTTATGAGACT | 51429 |
| rs529916534 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157801813 | AGAACGCGTGCTCTG[A/G]CAGAAAGAACTGCTT | 51429 |
| rs529925576 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157747803 | TGAATTATTTTTATT[C/T]GTTTTAAATAAAACA | 51429 |
| rs529926126 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157933987 | ATTCAAGTTCCTGTT[A/G]ACTGGCTTTTCTCCC | 51429 |
| rs529973579 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157786217 | CTGGCTAAATTTTTT[A/T]TAAAATTGTTTGATA | 51429 |
| rs529980321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157740850 | CCTTCCAATTAGATG[A/G]GCCTGGAATCCTAGC | 51429 |
| rs529999995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157808469 | AAGATAAACTCAAAG[A/G]TCTAATATACATCTC | 51429 |
| rs530013477 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157923478 | AAAAGTATCAAATAT[A/C]CAGGAATAAATACAA | 51429 |
| rs530031519 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157767722 | TCATATGAAGATCCT[G/T]TTTTCTCTTTAATCA | 51429 |
| rs530052100 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157852704 | ACTTCTACCTGCCAA[A/G]TAGCTAGGACTACAG | 51429 |
| rs530075794 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157722039 | ATCCATAGCACTTTC[C/G]CATGAAGCCCGTTCC | 51429 |
| rs530080540 | snp | G/T | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893484 | TCTGCCCCATGTGTC[G/T]GTTGGTGAAGAGTCA | 51429 |
| rs530088654 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | SNX9, LOC107986663 | GRCh38.p7 | 6:157715241 | TTCTAATTGGATACT[A/G]ATGGCATAAAGAATG | 51429 |
| rs530104067 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157919725 | GCGGACACTCAGAGA[C/T]AGTGTCTATTGACTG | 51429 |
| rs530108278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157760897 | AAGCAGGTAGGGAGC[A/G]AGAGGGCAGGCTGGG | 51429 |
| rs530109738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157870418 | GTCACCTGCTCTCAC[A/G]CACGCACACTCACAT | 51429 |
| rs530114472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157858221 | TAAGCACATGAACTC[A/G]TCCGGAGTCTTTTTT | 51429 |
| rs530119312 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157823750 | GGGCTGCGGCGGGCT[A/C]GCCGGGAGGGGCCGC | 51429 |
| rs530128267 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157898227 | TTATTCACTAGTAGC[A/C]AACCTGGATTCAATT | 51429 |
| rs530129018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157910307 | GCTGTACCTTTTCTA[C/T]AAAAGAAATGTGTAC | 51429 |
| rs530139844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157772665 | TGTTTTAAAGCCACC[C/T]GCTTTGTGGTAGTTT | 51429 |
| rs530144689 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | SNX9, LOC107986663 | GRCh38.p7 | 6:157714167 | CTCCACCAGCTCATG[C/G]ACAATCTGGCAAAGG | 51429 |
| rs530169519 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157755692 | ACGACTTCAGAGTGA[C/T]TTTGATTTTCCATTC | 51429 |
| rs530189670 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157864608 | CAGGTTCCTCATGCC[C/G/T]GTGAGTGTGGCTTTG | 51429 |
| rs530190288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157816198 | ATGCAAATATTGACA[C/T]GGGAGGTAACGGGTA | 51429 |
| rs530213708 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157767212 | TCCCCTGCTCTGAGC[A/G]GTTGAGCTAGCACAA | 51429 |
| rs530217634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157844210 | ATTTCTCAGGACAAG[C/T]GGAATTGCAATAGAG | 51429 |
| rs530236380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157721259 | GCACTGCAGCCTGGG[C/T]GACACAGCGAGACCC | 51429 |
| rs530239235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157729968 | AGAACAGGCAAATCT[A/G]TAGAGATAGACAGTA | 51429 |
| rs530248351 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157825077 | ATATGGTGAAACCCT[C/G]TCTCTACTAAAAATA | 51429 |
| rs530253839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157865211 | AAGTGTGGTGGTAGG[C/T]GCCTGTAGTCCCAGC | 51429 |
| rs530253856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157857486 | AATCTTTGACCCATT[A/G]TATGATTTATTTTGT | 51429 |
| rs530272568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157756412 | CAACAGAGTGAGACT[C/T]TGTCTAAAAAAAAAA | 51429 |
| rs530274767 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157749643 | CCTGCCTCCACCTCC[C/T]GAGTAGCTGGGACTA | 51429 |
| rs530293188 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157725353 | TTCAACAAAATTGCA[C/T]ATTTTTCAACTCTTA | 51429 |
| rs530302206 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | SNX9, LOC107986663 | GRCh38.p7 | 6:157715070 | AAAAGAAGAAGAAGA[A/G]GCAGGTATCTATCTA | 51429 |
| rs530330309 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157787442 | TCTCTCTCTCCCCCC[A/C]ACCCCTCTCTCTGTG | 51429 |
| rs530337192 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157716907 | AAACAATATCAACAC[A/T]AAGCAAATTCAGTGT | 51429 |
| rs530340377 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157746538 | TATTTCTGCCCAATG[C/G]AGTACTCTGTTTTCA | 51429 |
| rs530342216 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157805291 | TGTCTCTCCCCTCTA[A/T]CCCTGGGGCCGCCAT | 51429 |
| rs530347135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157931138 | CCTCCTGTTTCTCAA[A/G]GTAGTTCTTTAAAAT | 51429 |
| rs530347175 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157938296 | CCTAGCCACATGACT[C/T]CCAAAACCTGCTAAT | 51429 |
| rs530354942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157802194 | TCCCCTCTGCCCTCC[A/G]CAGCTGCTATTGAAG | 51429 |
| rs530363672 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157925029 | ATGAAAAAGACTATG[C/G]AGGAAGATGTGGATA | 51429 |
| rs530368998 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157892351 | GCAGTAAAAGGCCAT[C/T]TGCTGAGGGACTGAG | 51429 |
| rs530381955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157850623 | GAAGTTGGGGTAAAG[A/G]TCATGGGCCTGTTAT | 51429 |
| rs530398059 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157870744 | CCTGTGCAAGCATGC[A/G]CACCCCTCAGACACT | 51429 |
| rs530400329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157891384 | ATTCTGTGATCGACC[A/G]CAACAAGTTAATTTT | 51429 |
| rs530427665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157812721 | TGTGCAGAGCAGGGC[C/T]CTCCCCAGCCTCCCA | 51429 |
| rs530447187 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157843779 | GCAATTCTAATTTTT[G/T]GTTTCTTTTAGAAGA | 51429 |
| rs530451735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157794463 | AAGTCATTAGTTCAC[A/G]GTAAAGGCAGGGCTA | 51429 |
| rs530484622 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157732218 | TCTAGTTCCTCCCAC[C/T]AAGAATGCAGGACAT | 51429 |
| rs530488257 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157774541 | CGGTCATCGACCCAC[A/G]TGTCTGCCTTAGGAA | 51429 |
| rs530501145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157819208 | TTTATTCCTATAAAG[A/G]TTCTTCAGAGCACTT | 51429 |
| rs530506844 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157763724 | TATTGACGATTCCTC[A/C]AAACACCAAGGGGAG | 51429 |
| rs530523926 | snp | C/T | 0 | 0 | downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157945376 | TTTCTTACAAAAGTA[C/T]CTGCTGGGTCTGGGG | 51429 |
| rs530552340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157764096 | GGACTATTTCTGATC[C/T]AGATGCTGTACTAAA | 51429 |
| rs530563255 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157725713 | TCAACTGAATGTCAG[A/C]GATTACGGATAGACG | 51429 |
| rs530595395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157867103 | ACAGGTGCTGGCTAC[A/G]ATGCCCAGCTAATTT | 51429 |
| rs530598186 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157873712 | ATCTATAATATTGTT[G/T]ATTGTACAATAGACT | 51429 |
| rs530604925 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157935178 | TCAAACTCTACCTCT[C/G]GGTAACCGGAATATT | 51429 |
| rs530617734 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157740216 | TTTTGTGCAAGGCCA[C/T]ATTGCCCAACTCCAA | 51429 |
| rs530660271 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157867427 | TTCCTTTCTTCCAAA[A/G]CAGCCACAGCCACTA | 51429 |
| rs530666352 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157839504 | AAAAGTTACTTACTG[A/C]TTCACTTTCCTTATC | 51429 |
| rs530674928 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157853781 | TACATGCAAATGTAC[A/G]TGTAATGTTTAAAAA | 51429 |
| rs530675286 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157759237 | TTCTGAGTCATGCAG[G/T]CTGCGGGCAGGGGAC | 51429 |
| rs530688647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157895028 | TCACACTAGAGTCAC[A/G]TATATTTAGGAGTTT | 51429 |
| rs530705294 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157810469 | CTAATAAAGCTGTTG[A/G]GAAAAAATTCCAAGG | 51429 |
| rs530712817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157804826 | GTTGGTTGAATCCAG[A/G]ATGTGAGCTGGAGCG | 51429 |
| rs530716296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157847356 | GATCTGCCCACCTCC[A/G]CCTCCCAAAATGCTA | 51429 |
| rs530731457 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157764584 | AAGAAAAAAAATCCG[A/G]ATGTTTTTGTCATAT | 51429 |
| rs530736604 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157846659 | ACCCTGTCATTTTTC[A/C]TGTGTGAAAGCTGAG | 51429 |
| rs530744939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888560 | TCACTGGGCACCTTT[C/T]TTATTTTAAGGTGGA | 51429 |
| rs530756920 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157798679 | GCTTATTTCTACAAC[C/G]TTTCTCTAAGCTTGA | 51429 |
| rs530768021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157828236 | TTTGTATAGTCAAAG[A/G]TAAGTTCTGTGACAG | 51429 |
| rs530768634 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157857594 | TTATCATGTTACCTA[C/T]GTTTCTATATGTCTT | 51429 |
| rs530786616 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157775966 | TTTGGCGGTGACATT[G/T]TCTGCCCCAGATGAA | 51429 |
| rs530815756 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157740065 | TAACAAACCTGCACA[A/T]TCTGTACATGTATCC | 51429 |
| rs530839801 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157758551 | AGACACTCTTGGTGG[A/G]GGCAGAGGAAGGGGA | 51429 |
| rs530852302 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157820739 | TGGAGTGCAGTGGCT[C/T]GATCTCGGCCCACTG | 51429 |
| rs530889095 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157878228 | TCCTCTTTTGGTGGT[A/G]AGAAAACGCTTTATC | 51429 |
| rs530902635 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157784618 | GATCCTCCTGCCTTG[C/G]CCTCCCAAAGTGCTG | 51429 |
| rs530920693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157920769 | CTAATAGTAGTTTTT[A/G]TTTGTAGGTTTATAA | 51429 |
| rs530953047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157874586 | TTGATGTCCACTTAG[A/G]GACATCTATAGACTG | 51429 |
| rs530962482 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157914630 | TACAGGCTCTCATCA[A/G]CACTTCTTGTTAATT | 51429 |
| rs530968946 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157779465 | AAGACAAAAAGTTAA[A/T]GTAAATGTCATTTTA | 51429 |
| rs530996730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157791544 | ATTTTGCTTATGAGT[A/G]TTTTTGAAAAGCTGT | 51429 |
| rs531003955 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157811902 | TGAGATTGCAGTTAG[C/G]TGTCACCCAAGGCTG | 51429 |
| rs531011442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157746005 | TCATTAAAATCTGCT[A/G]TCCCTGGAATTTTGG | 51429 |
| rs531032553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157896370 | TCCTCATGTTGAGTG[A/G]GAAAAAGAAAACTTG | 51429 |
| rs531036328 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157723003 | GCAAGACTCTGTCTC[-/A]AAAAAAAAATTATAT | 51429 |
| rs531038695 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157765992 | TTGTCATCAAGACAA[C/T]ATTTACAGCACACAC | 51429 |
| rs531046037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157928816 | AGTGTATTTGGTGGA[C/T]GGCAGTAATGTCCCT | 51429 |
| rs531049046 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157923505 | ACAAGAAAATGTACA[A/G]AAGATCTACATAGAA | 51429 |
| rs531059975 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157772460 | ACAGGGATGAAGGCC[A/G]AGTGAAAAGGGAGGC | 51429 |
| rs531065016 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157783904 | CGCCTCAGCTTCCCA[C/G]AGTGCTGGGATTACA | 51429 |
| rs531073685 | in-del | -/AC | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157843375 | TAACGCAAACAGTTA[-/AC]ACATATTTTGTATGT | 51429 |
| rs531091377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157814666 | GTGGCCCCACAAATT[A/G]TGCAGCCAGTCCTGA | 51429 |
| rs531119083 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157790855 | TGTCTTTCTGGTTCT[C/T]TGTTCTCTCCCTAAG | 51429 |
| rs531121732 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157765577 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT | 51429 |
| rs531129511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157806404 | GTGAAACATTATTCC[A/G]TGGATATAATTTTGG | 51429 |
| rs531131665 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157792152 | TTCCTTCCTTCCTTC[-/T]TTTTTTTTTGATACA | 51429 |
| rs531133663 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157944687 | GGTCAGTGTTGCGGT[A/C]CGGGAAGCGTATCAT | 51429 |
| rs531145627 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157863435 | TGAGATTGATGTCTA[G/T]TAGCCATTCATGTCA | 51429 |
| rs531147661 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | SNX9 | GRCh38.p7 | 6:157750139 | AACAATAGAAAAAAA[A/T]TTTTAAATTCATATG | 51429 |
| rs531164778 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157838213 | AGATGGTGTTTTGCC[A/C]TGTTGCCCAGGCTGG | 51429 |
| rs531173334 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157906558 | ATATTTATGTTTCTT[C/T]CCTTGTAAAGTACAT | 51429 |
| rs531186398 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157924972 | GATAACGTGGAACAT[A/C]CTCCTATCCTAGAGA | 51429 |
| rs531214503 | snp | C/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885896 | TGCGACCACTCACAG[C/T]ATGTTTTGAGCTTTC | 51429 |
| rs531215068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157821088 | ACTATGTTGCCCAGG[C/T]TGGTGTTGAACACCT | 51429 |
| rs531219589 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157870525 | ATGCACTCACCTGTG[C/T]AAGCACGCACACCCC | 51429 |
| rs531260618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157727687 | AGCTTTGGGAGAAGA[C/T]TGTGTAGGAAGTGTG | 51429 |
| rs531283010 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157748680 | GTTGCAGTGAGCCAA[A/G]ATCATGCCACTGCAC | 51429 |
| rs531316900 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157787897 | CCAGCACAGTGCTGG[A/T]TATAAGCAGTGTTCA | 51429 |
| rs531324266 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157837602 | CTTAGAAGCTTTAAG[G/T]AAGTAAAGAAACAAA | 51429 |
| rs531332716 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157747577 | ATTGTATTAACTACT[C/T]GTTCGAGGCATATTG | 51429 |
| rs531368655 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157728189 | GCTAGGGATGACCTG[G/T]AAAAATGTAATACAT | 51429 |
| rs531382779 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157823974 | CGGGGAGGGACCGAG[G/T]CTGGGACGCCCCGCG | 51429 |
| rs531397950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157866481 | GGGGAGGCTGAGGTG[A/G]GAGGATTGCTTGAGC | 51429 |
| rs531445180 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157924348 | GGGCAGCTTTTCCCT[G/T]GGCCACATGTGCTGA | 51429 |
| rs531478123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157871008 | AGATCGAGGAGGGAG[A/G]ATGAGGAACGGCAGA | 51429 |
| rs531480051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157787311 | CTCAAACTGGAGTTA[C/T]GCCATCAGCTCTCCT | 51429 |
| rs531500702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157911942 | TCTCCCCAGTCCCCT[A/G]GGTGACACTTGAGTG | 51429 |
| rs531511920 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157773289 | TCCTTGACTGCAGCC[A/C]GGGTGCTAGGCCCCA | 51429 |
| rs531532053 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157943405 | ACACTTCAAGAGGGA[C/G]GACGCTGGGGGCCCC | 51429 |
| rs531542694 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157818222 | CTGAGTCCCAAAACT[G/T]AAGAACTTGAAGTCT | 51429 |
| rs531551041 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157815635 | TTTGCACATTGTAGG[C/T]TCTCAATAGATAGCT | 51429 |
| rs531556050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, nc-transcript-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157893143 | TAAAACTACATTTCC[C/T]TAAAGAAAACTGTAG | 51429 |
| rs531615510 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157860916 | GAATTTGTAATTCTA[C/T]TCAGGGAATTTCTAT | 51429 |
| rs531616438 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157773089 | CTGGTGAGCATATTT[A/G]TCCTCTAAACACATT | 51429 |
| rs531617847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885923 | TTTCATAGACCCTTT[A/G]TACATGTTTGGTAGA | 51429 |
| rs531641833 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157911194 | TTTTAGTATATTGCT[A/G]GAAAATGTTCACATA | 51429 |
| rs531649781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157750849 | ATGCAAATGGCCAAC[A/G]GGCATATGGAAAGAT | 51429 |
| rs531673820 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157943995 | AAAGAACAGACCAGC[A/G]CCCTTCCCGACTACA | 51429 |
| rs531677716 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157863877 | TTTTTATTGACATGT[C/T]ATACTTATTTGGAGA | 51429 |
| rs531689200 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157769949 | GCTTCACGGGCAGGT[A/G]AGCTGAGCCAGCGCA | 51429 |
| rs531708860 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157762822 | AGAGGAAGGCTGCTC[A/G]GTGAGGCTTGCCCAT | 51429 |
| rs531720733 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157794371 | ATAAATTACCCTGTC[C/T]CAGGTATGTCTTTAT | 51429 |
| rs531757593 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157771000 | AACTTAAGATGTAAC[A/T]CAATAAGCTCATTAT | 51429 |
| rs531774630 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157931252 | TGAGGTACCACAGGG[A/G]TACAATTTATTAAAA | 51429 |
| rs531775897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157845624 | CAGAATTTCCTGTGT[A/G]TACTAGAGAGTATCC | 51429 |
| rs531779673 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157925832 | TAACAAAATACCTGA[G/T]ACTGGATAATTTATA | 51429 |
| rs531790979 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157715746 | TCCTCTGTGTATTTG[C/T]CATGGGTTTCATCTG | 51429 |
| rs531819036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157872849 | AGACAAGATGAGGGT[C/T]ATCTAATCATCAGCT | 51429 |
| rs531819727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157912734 | AATGTACAGTTAACA[C/T]TTCTTTATTTGTTTA | 51429 |
| rs531831197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157802630 | ATTATTATAGGATAG[C/T]TCCTTTTTGTGTTTG | 51429 |
| rs531840838 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | SNX9 | GRCh38.p7 | 6:157811061 | ACCCTGTCACCAAAA[A/C]AAAAAACAAAAAACA | 51429 |
| rs531844498 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157775232 | GCGTGGTGGCACACA[C/G]CTATAGTCCCAGCCA | 51429 |
| rs531846360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157756565 | TTCATTGCTCCAGGC[A/G]CAGAGTTCTGGATTG | 51429 |
| rs531853163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157826270 | TTGGGAGGCCGAGGC[A/G]GGCGGATCACGAGGT | 51429 |
| rs531864322 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157938956 | GGCTATAGATGACAG[A/C]TTGATTAAAACTGTA | 51429 |
| rs531868518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886620 | TGTTATTCCTTCCAC[A/G]CTTAGCTGGTTTCAT | 51429 |
| rs531905126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157737784 | CGCTTTCTCCTGTGG[A/G]CATTTACTGCTATAA | 51429 |
| rs531917316 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157925090 | GCCATGACAAGCGAA[A/C]AACAAGCTACTGAGT | 51429 |
| rs531922095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157780630 | CTTGCTTCTCTTACT[A/G]CTATTGCATGAATCA | 51429 |
| rs531934492 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157896232 | TCTCAGGATGTTAGG[A/C/T]GTATTTCTCAAATTG | 51429 |
| rs531940618 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157846022 | AGGCACAAAGGATCC[C/T]GGCAAAATTCTGGTG | 51429 |
| rs531941503 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157871465 | TTCTCATTCATAGGT[A/G]GGAATTGAACAATGA | 51429 |
| rs531942417 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157738369 | AGCTCTTCTTGTTGC[A/G]TTGATCCCTTTACCT | 51429 |
| rs531955751 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157879813 | TATAGATCTTAAACT[C/G]TCAGATTACTGCTTC | 51429 |
| rs531966431 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157919813 | TTTTGTTGAAAACTG[A/G]ACATTTTTGAGAATA | 51429 |
| rs531990848 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157753803 | AATTCATCAAGACAC[A/G]GGAATTGCAATAGAG | 51429 |
| rs532000050 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157935620 | TGATTCAAGCAGCCA[C/G]CTCTCCCTGAGAGGC | 51429 |
| rs532009649 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157751589 | GGTAAAGAAAATGTG[A/G]TGTGTACATAAATGG | 51429 |
| rs532013735 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157879098 | TGAAGCTTTTCGGGG[C/G]TGGTTCGGTAATGTA | 51429 |
| rs532026005 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157845990 | GTGTTATTGATTTGC[A/G]AGAAGGATCAGCTGG | 51429 |
| rs532038609 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157751421 | TATCAGGAGGTTCTC[A/C]AAAAATTAAAACTAG | 51429 |
| rs532057301 | in-del | -/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157741378 | ACAAAAAAAAAAAAA[-/G]CAGAGAATCACATGT | 51429 |
| rs532060964 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157868797 | GGAACAAAAGCAGAT[A/G]GGGAGAATTTGTCTT | 51429 |
| rs532107368 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157805838 | TCTGTATTCTTTTAC[A/G]TGTATATTCAACCAT | 51429 |
| rs532121731 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157870069 | GAGCACGCACACACA[A/C]CCTCTTCACTCTCAC | 51429 |
| rs532123200 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157759459 | CAACACTTTGGGAGG[C/G]TGAGGCTGGTGGATC | 51429 |
| rs532126667 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157848248 | AAAATATAAACATAC[C/T]GGCTACCTAGCTTCA | 51429 |
| rs532133034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157941877 | GCCCTGTCCTCCCTT[A/G]CAGGACGTGGGCCCT | 51429 |
| rs532152392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157922483 | AAATAATAGAATATC[A/G]TATACCCTCTTGGAA | 51429 |
| rs532154717 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157774820 | AGGGAGAGAGGGATC[A/T]CACTTCTTCCCACTG | 51429 |
| rs532169168 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157753899 | TCCCTGATCATTGGG[C/G]AGCAGAGTTTTTAAA | 51429 |
| rs532177612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157841745 | GCTTCTGCTACGACA[A/G]GGTCCCACTTATCTT | 51429 |
| rs532187521 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157863413 | AGTAGTTAATGGAAC[A/T]GATACGTGAGATTGA | 51429 |
| rs532196113 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157718413 | GTGTATGAGCGTTTC[A/C]TTTTTCCCACATCCT | 51429 |
| rs532208598 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157937807 | GTATATTATGATGTA[C/G]TTGGATTTGTTAGGA | 51429 |
| rs532223372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157901279 | GGGGGTCTCCCTACA[C/T]CAGCCCATAGGCTAC | 51429 |
| rs532233109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157792213 | GTGGTGCCATCTAAG[C/T]TCACTGCAACCTCCG | 51429 |
| rs532240044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157814545 | TGGGCCTATACAGTT[C/T]ACAGGGCCTCAAGAA | 51429 |
| rs532249900 | in-del | -/AG | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157870604 | GCACACACACCCCTC[-/AG]ACACTCTCACCTGCC | 51429 |
| rs532251896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157855661 | GACTCGTACTCTTTA[C/T]ATAGAGTAGCAGGAG | 51429 |
| rs532262578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157719287 | AAATAAGGTTTATCC[A/G]GAGAGGCTCCAGAAG | 51429 |
| rs532265384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157800110 | TTGAGAGCAGTTTGT[A/G]CTTCATCTGTTTAAA | 51429 |
| rs532307243 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157740322 | TAGAACAACTTGGAC[C/T]GCTCTTGACAAGGAA | 51429 |
| rs532309088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157747226 | TACAAGAAAGTAATG[C/T]CCCCACACAAACCAG | 51429 |
| rs532318011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157792616 | ATTTTTGAAAATATA[C/T]TTTTATTAACTAAAG | 51429 |
| rs532327077 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157754619 | ATGCATGTTGTGAGC[A/G]TGGACATCAGCACGT | 51429 |
| rs532341303 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822828 | CTGCCGCCCCCTCCC[A/G]CCTCATGCACGGAAA | 51429 |
| rs532345031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157784946 | ACCCAACTCTTAGGA[A/G]ATAGAAAAGAAAAGC | 51429 |
| rs532359075 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157916780 | GAATAAACCTCACTC[A/G]ATGGTGATAGATTAT | 51429 |
| rs532367695 | in-del | -/TCA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157780665 | TATTCAAACAATTAT[-/TCA]TCATTTATCTGAAAT | 51429 |
| rs532371764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157913618 | ACATTTCATGATACA[A/G]AACAGCTCCGTCACC | 51429 |
| rs532380071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157735417 | CAGACCTGGCCGGGC[A/G]TGGTGGCTCATGCCT | 51429 |
| rs532383596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157829177 | AAACATAATCAATTT[C/T]ACTAATGATTACATG | 51429 |
| rs532384398 | in-del | -/AA | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157736450 | CATGATTTGGCTCTC[-/AA]TGTTTGTCTGTTATT | 51429 |
| rs532392676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157772431 | CCTAGAAGAAAAGAA[A/G]ATGGGGGCCAAACAC | 51429 |
| rs532397434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157740826 | GAAGTAACATGGGAA[A/G]AATGCAGGCCTTCCA | 51429 |
| rs532409158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157720135 | GTCTGGTCGCAAGGT[C/T]TGCTATATGAAATGC | 51429 |
| rs532441210 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157729396 | CCCACTGTCCCCACC[A/G]CGCAGAACTAGGATG | 51429 |
| rs532452096 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157929396 | AGAGGCTGCAGAGTG[A/G]CTTGTCAGGCCCTGA | 51429 |
| rs532467735 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157842149 | TTCAAATATCCAGTC[C/T]GTTGGTAGGCAGTGT | 51429 |
| rs532472314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157746614 | CATCCTTATCCTGGG[A/G]CAAGACAGAGATGGA | 51429 |
| rs532473957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157916111 | GCTATCTCGGCTTAC[C/T]GCAAGCTCCACCTCC | 51429 |
| rs532484701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157829871 | TTTACTGATATATTT[A/G]GATTTCTGTCTACCA | 51429 |
| rs532505425 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157777837 | GTGGTGCTCCGTATG[C/T]AGCTGCTCTCAGCAG | 51429 |
| rs532541921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157766303 | ACTTAGCCACTCACT[A/G]GCGCTTCCCCTGGAA | 51429 |
| rs532553158 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157937454 | GAAAGATCTCCATTT[C/T]CTGATGGAATGTAAT | 51429 |
| rs532579197 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157850526 | ACAGTCCCAGTGCAA[A/C]TGGGTGGGCTCACAT | 51429 |
| rs532580530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157767038 | TACTAGCGCTGCTTC[C/T]CCTCCTTGACCTAAT | 51429 |
| rs532604638 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157777302 | GGAGAATGGTGTGAA[A/C]CTGGGAGGTGGAGCT | 51429 |
| rs532609961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157759950 | TTGGCTCACTGCAAC[C/T]TCCACCTCCCAGGTT | 51429 |
| rs532617862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157721153 | AGGCATGGTGGCACA[C/T]CCCTGCAATTCCAGC | 51429 |
| rs532627704 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157942433 | TTCAGGGGATTCTGG[A/C]AGCTCATACTCCTCC | 51429 |
| rs532635363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157755899 | AAAGTTCAGATGCTA[C/T]GGAAAGACAGTGTGG | 51429 |
| rs532644556 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157772000 | CACTGCACCCGGCCC[A/G]GCAGCCAAATTTTAA | 51429 |
| rs532688890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157869922 | CTCGCACCCTCATAC[A/G]CCTCTCATGCTCTCA | 51429 |
| rs532690038 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157936879 | TCTAATCCCTTAATT[A/T]AAAAAAATTTTTTTT | 51429 |
| rs532691813 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157942684 | AAGACCAGTTAAAGA[A/G]TTGGAATTTGTGTCA | 51429 |
| rs532692437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157755249 | AGCCCAGTAGGTCTC[C/T]GCCTCATTTTACCCA | 51429 |
| rs532694832 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, nc-transcript-variant | SNX9, LOC107986663 | GRCh38.p7 | 6:157714462 | GAACAGGTCCTCTTC[A/G]TTCTCTGCCCTAAGG | 51429 |
| rs532706514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157761382 | CAACATGTATCAAGC[A/G]GTCTATGATGTGCTG | 51429 |
| rs532712712 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890766 | TCAGACGAGAGTGAT[C/T]GTATATGTCGATTTT | 51429 |
| rs532715684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157858077 | CGGATCTGCAGAGTT[A/G]CTAACCCAGCCAGGT | 51429 |
| rs532741085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157818497 | ATCAAGTTGACACTC[A/G]GTTTTAACCATCACA | 51429 |
| rs532741179 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157826237 | CGGGCGCCGTCTCAC[A/C/G]CCTGTAATCCTAGCA | 51429 |
| rs532755644 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157912640 | GAATTCCCCTCTCGC[C/T]CAACTACTGGAGAAA | 51429 |
| rs532776204 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157819089 | ACCAATCAGCTAACC[A/T]ACTAAAACAAACATA | 51429 |
| rs532811400 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157718171 | ATGTACCACTTTTTA[A/G]TCCAATCATCTGGTG | 51429 |
| rs532817497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157905941 | TGTTTACCAGATCAA[A/G]CTTAATTAAATGCCT | 51429 |
| rs532835293 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157771349 | CTAGTAATACAGTTA[A/G]TAGGAAGAGCTTTAA | 51429 |
| rs532840991 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157808196 | GAGATTACAATAGAA[A/C]TGGAAATGGCTGGTA | 51429 |
| rs532844367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157780553 | TCAGTTAAATTTTCC[A/G]GGACTCTCTGTTAAA | 51429 |
| rs532845939 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157897620 | TCAAGTGATTCTCTC[A/T]CCTCAGCCTCCTGAG | 51429 |
| rs532850643 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157825583 | CTCCAAAGGCAAATT[A/C]CAGTAGTTCTGTTAG | 51429 |
| rs532859435 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157849771 | ATCTAGAAGGCTGGG[C/G]AATGCTGGAGAGAAG | 51429 |
| rs532869880 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157737691 | ATTTCTTGTCTTCTG[C/G]TAGCTTTTGAATTTG | 51429 |
| rs532870784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157760743 | GATCAGGGCAGACGC[C/T]AGCTGGTGGCCTGGT | 51429 |
| rs532895898 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157784554 | ATTTTTAGTAGAGAT[A/G]GGGTTTCACCATGTT | 51429 |
| rs532911854 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157738260 | GTCTCCTACTATTAT[G/T]GTGTGGAAGTCTAAG | 51429 |
| rs532947090 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157731821 | AGGCACTTCCAGCTT[A/G]GAGCCCAACTAGGTT | 51429 |
| rs532949900 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157867045 | CTTTGACCTCCTGGG[C/G]TCAAGCAATCCTCCC | 51429 |
| rs532955831 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157744176 | CAGCAGCTATTCTTT[G/T]TATATGATCATAATG | 51429 |
| rs532974898 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157721093 | TGAGACCAGCCTGGC[A/C]AACATGGTGAAACCC | 51429 |
| rs532980991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157757925 | AGGTCTCAGGAGGAA[C/T]GGTAACAAGAAGACT | 51429 |
| rs533001597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157846502 | TTGTATATGTATTTA[C/T]GTCGATGACCTTAAG | 51429 |
| rs533009839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157879605 | TATTAGTTTCATTAT[C/T]AGTTACTTATCGGTT | 51429 |
| rs533011507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157725082 | ATAAGATTCCTGGTT[A/G]ACTTTTTTTTCCCGA | 51429 |
| rs533032276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157860514 | GTATCTGTTTTGACA[C/T]ATTACTTGGTAATCG | 51429 |
| rs533047737 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157912041 | GAGGCACTGACCGAA[C/G]CCCTGCTTCTAACCC | 51429 |
| rs533070788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157811972 | TGCAAGCTCAGTCAT[A/G]TGACTGTTGGCAGGC | 51429 |
| rs533075712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157716984 | CGTCTGTCATCTCCG[C/T]ACTTGCTGGGCTGCA | 51429 |
| rs533075770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157852956 | TAAAAGTCAGTTATC[C/T]TCTTAGTTTTCTTTC | 51429 |
| rs533084061 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157945245 | AAGAAAGATGACTCA[C/G]AGAGGCACTGGGTGG | 51429 |
| rs533084796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157763631 | TCACCCGGCTCCATA[C/T]ACCTGCCTGATTCCA | 51429 |
| rs533092783 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157781509 | AAATTCTCTGGAAAA[A/C/G]GATGATTGTGGAGAT | 51429 |
| rs533104507 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157773913 | TGAGGTGCTATGGCA[A/C]GATTAATTGGAGAAA | 51429 |
| rs533113486 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157837077 | TGCCGTGTGCAGTGA[A/G]CACTTGTGTCTTGCT | 51429 |
| rs533115558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157840898 | CATTTGGCTGTTACC[A/G]TTATGCTGTTCACTC | 51429 |
| rs533115734 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | SNX9 | GRCh38.p7 | 6:157745080 | GATGGAGACCTCTAC[A/C]ATAAGCAAAGGAAGA | 51429 |
| rs533124379 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157880979 | TTAATAATTGTTAAT[C/T]ATAGTTATCTCATAT | 51429 |
| rs533128424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157853727 | TTCCAGAACCTTTGG[C/T]GGACTGGAAAGAGGA | 51429 |
| rs533133566 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157810596 | TGTTCCCTTAACTCT[C/T]CGGTTATTGCATTGT | 51429 |
| rs533134732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157834146 | CCATGTGGTGTCCAC[C/T]GTGGTTTTTTTTTTT | 51429 |
| rs533136206 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157900299 | GGGTCCTTTGTCCAT[C/T]TTTTAATTGAGCTTT | 51429 |
| rs533153061 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157782807 | CAGAGAACTACCTAA[A/T]CCCCAGAGGCGGAGG | 51429 |
| rs533156477 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157764039 | TTAAAGCTCTGTGTA[C/T]GTATCATGCAAATGT | 51429 |
| rs533165738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157873920 | AGCCAACCACCTGGC[A/G]CCCCCTGCTGGTTGT | 51429 |
| rs533185666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894357 | TCAGGTGATCCTCCC[A/G]CCTCGGCCTCCGAAA | 51429 |
| rs533189171 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157758463 | TGGATTCGAGAGCGG[A/C]AAGTCTGGGGATAGG | 51429 |
| rs533201465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157745847 | AACTGCTCCACCCCA[A/G]GAGCTCCTGAAAGTA | 51429 |
| rs533221594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157881594 | TGTGACTGCAAAGGA[A/G]AAGTTCTTGAAGGAA | 51429 |
| rs533227023 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157937941 | AATTAGGTTTGTACA[A/G]CTTCAGATAACTTAA | 51429 |
| rs533243758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157906317 | AAAGTATTTTTAAAT[A/G]TATTTAATGCCCCAC | 51429 |
| rs533253724 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157899807 | ATTTGAGGTATACAG[C/T]GTGATGTTGTAATAT | 51429 |
| rs533254725 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887710 | GCATAAACTGGGTCC[C/G]TGTTACTCCATCTTT | 51429 |
| rs533259725 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157922444 | CCTGGGAAATAAATT[A/G]TGAAGCTATTTTTGT | 51429 |
| rs533272232 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157840381 | GTTTTCACCACACCC[A/G]AAATGACTGACTTTT | 51429 |
| rs533274550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157752385 | TCTCTGAGTTCCCTC[A/G]GTATTTATTGATCAT | 51429 |
| rs533275445 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157861659 | GATATGCAGTAGTCC[C/G]CCTTTAGTGACGGGG | 51429 |
| rs533289905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157812607 | AATGGTTTCCCTCCT[C/T]CCCTATATGCCAGCC | 51429 |
| rs533295117 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157834615 | CTGTGTCAGCCTCCC[A/G]AAGAATTGTGATTAC | 51429 |
| rs533336197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157927944 | TAACACACACACACA[C/T]ACACACACATAACCC | 51429 |
| rs533358317 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157862684 | TTGCCAGGGTTTTGT[C/G]AATTTTTTTTCCTTC | 51429 |
| rs533380488 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157868101 | TCATCATTTTTCTAA[G/T]CTCTTTTCCTAAATC | 51429 |
| rs533381984 | snp | A/G | 0.000148969 | 0.00862917 | missense | SNX9 | GRCh38.p7 | 6:157928648 | AAGGCCATGGATGAC[A/G]GCGTGAAGGAGCTGC | 51429 |
| rs533383587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157905098 | AGCCCCTAAGGCTAC[C/T]TAAGTGTTGGAGTCA | 51429 |
| rs533390383 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157900726 | GAGATAAGAATTTAC[A/T]ATATAGTGTATGCAT | 51429 |
| rs533409515 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157827671 | AAGTTCTGGAAAAGA[A/C]ATGAAGAATTTTTTT | 51429 |
| rs533426457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157775038 | GGGCCGGCTGTGTTG[C/T]TGATCAACACAAACG | 51429 |
| rs533479733 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157868099 | TATCATCATTTTTCT[A/C]AGCTCTTTTCCTAAA | 51429 |
| rs533510046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157790539 | GAGACTGGCACACAA[C/T]CCCACTCCCCCCACC | 51429 |
| rs533517594 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888470 | AGTGGCATGCTAGAG[A/T]TTTCTGGAGAATTTG | 51429 |
| rs533528390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157914589 | TCAAGCAGTCTTCCA[C/G]CCTCAGCCTCCTGAG | 51429 |
| rs533542467 | in-del | -/TGTT | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157919739 | ATAGTGTCTATTGAC[-/TGTT]TGTTTTTTTCTCAGT | 51429 |
| rs533546244 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157869678 | TCTGTCTAAACGGCC[A/C]GTGTGGCCAGGTCAT | 51429 |
| rs533547025 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157733187 | CTGGCTTACAAAAAT[G/T]TGCCTGGTGGGGCCG | 51429 |
| rs533553957 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157833109 | GTATTTAAAATGTGC[A/G]AGTTTAAATGTATTT | 51429 |
| rs533556960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157734984 | CAAGGTCAAGAAGGG[C/T]CTCCTGGCTGGGCCG | 51429 |
| rs533563453 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157771831 | CACCCACTGGAGTAG[C/G]TGGGATTACAGGCAC | 51429 |
| rs533583411 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157747804 | GAATTATTTTTATTC[A/G]TTTTAAATAAAACAA | 51429 |
| rs533599640 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157908058 | ACAGCCTCTGAACTT[C/T]AATATCCCAATCCGC | 51429 |
| rs533606097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157727013 | GAGGCTTCAACAGTT[C/T]ATCTGGAAGGAGGCA | 51429 |
| rs533625418 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157936125 | TGTCTTAGGACAAAC[A/G]TCCCAAATAAGTACC | 51429 |
| rs533627583 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157883171 | TTGACTAGTGGAAGG[C/G]TCAGATGATCGTTAG | 51429 |
| rs533645418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157783743 | TCTGCCTCCCAGGTT[C/T]AAGCAATTCTCCTGC | 51429 |
| rs533646939 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157884091 | ACACCGACCACAGGC[C/G]TAGGAGCTGTCCATC | 51429 |
| rs533659760 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157828205 | TTTCTATGTGTCTTA[A/C]GTAGAGTGTGCAGTA | 51429 |
| rs533661208 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157861830 | ATAATAAAATAGAAC[A/C]GTTATTATAGTATGC | 51429 |
| rs533662656 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157747343 | TGAAAACAGTCTACT[C/G]TCTTAGCCATGCTTG | 51429 |
| rs533673544 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157836492 | GAGCTGTGGTACTCT[A/C]ACTAGCTGTATCACA | 51429 |
| rs533703489 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157770750 | AGCTTGCAGTGAGCC[A/G]AGATCGCGCCACTGT | 51429 |
| rs533703708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157897396 | GGAAGGGACGCAGAG[C/T]TTCCATGCCCCCCTG | 51429 |
| rs533718892 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157924253 | TAGCTTTAAAGTAAG[-/A]AAAAAAAAAATCCCA | 51429 |
| rs533721271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157816294 | TAAGCTAGAATTTCT[A/G]AAGAGTATAACAATA | 51429 |
| rs533723419 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157869527 | TCACTTAAAGCCATT[C/G]GTTTCTCTCCCTAGA | 51429 |
| rs533732079 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157829395 | TGTACCTGGAAATTT[G/T]TTGAGGCTAACTTTA | 51429 |
| rs533732166 | snp | A/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821624 | TTTTTTACATAAATG[A/T]ACCATACATAATGTT | 51429 |
| rs533742277 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157837895 | TGAACAGCATATGCT[A/G]TACCATTAATTATGG | 51429 |
| rs533754785 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157808602 | GATCTGAGCCCATTA[A/C]ACATGTTTTCTTTGC | 51429 |
| rs533763699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157897773 | CACCTGCCTCAGCCT[C/T]CCAAAGTGCTGGGAT | 51429 |
| rs533773291 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157734508 | GCTTCTCAGCTGGGA[C/G]GCAGCAGCACCCAAG | 51429 |
| rs533795782 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157772224 | GGATGGGTCAAGGAT[A/T]TCTGGGGTGAAGGAG | 51429 |
| rs533821911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157909122 | TGATTAATCGTTTCT[A/G]TGAGCCAGAACAATG | 51429 |
| rs533829148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157922025 | AGTGACTGATTTTCC[C/T]GATCACGTTGCCCTT | 51429 |
| rs533839087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157902566 | AGCCAGGCCCTCAGG[C/T]GCCAAAGCACGTGTT | 51429 |
| rs533846010 | snp | C/T | 3.29506e-05 | 0.00405884 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157909997 | GTCAGCCATTCCAAT[C/T]CCTTCTCTTCCAGAC | 51429 |
| rs533871611 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157858883 | ATGGGGGATACCACC[C/T]CCATGATTCAGTTAT | 51429 |
| rs533880535 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157772494 | GAGTGGGGTGATGCA[G/T]CCGCAGGCTAAGGAC | 51429 |
| rs533884036 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157835990 | GTGGAGTGCCGTGGC[A/G]TGATCTGGGCTCACA | 51429 |
| rs533897055 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157913166 | CTTTGTTTCTGCTTA[A/G]TCTACTGCTAGTAAA | 51429 |
| rs533910162 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157753980 | CAGAGATGAAATCAT[C/G]GGGAGTCAAAGCTGT | 51429 |
| rs533945934 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157732573 | TGTGGTGATAACACT[C/T]TAGATCAACTCTCTT | 51429 |
| rs533954161 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157729609 | GCTGAAAAAAATGGA[A/T]GGTGAGTTAGAATAA | 51429 |
| rs533957281 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157807633 | GGATGAGGTCAGGAA[C/T]TGGATTTGCATTTAG | 51429 |
| rs533964603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157884581 | AGGTTCTTTCCATCT[C/T]TTCACTCTCACTCCC | 51429 |
| rs533969054 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157849277 | AATTACACTGAGATA[A/T]CAGGCATAAACTGGG | 51429 |
| rs533991331 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | SNX9, LOC107986663 | GRCh38.p7 | 6:157714295 | TCAGAAATGCAATAC[C/T]TCATTGACTTGTATT | 51429 |
| rs534017367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157898284 | GTTCAGTCTTACTTA[C/T]CTGTGTGAAGTCACA | 51429 |
| rs534025091 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157801313 | GCATTTATATGTTAC[A/C]TATTTTTTCATAATT | 51429 |
| rs534059073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157793845 | ACAAAAATATTTTGA[A/G]GGGTGGCCCCATCAG | 51429 |
| rs534061011 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157864324 | CCCATTTGCCGCACC[C/T]CCCAATACCACTGCC | 51429 |
| rs534061677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157937730 | CTTTTTAAAAATCTG[C/T]ACATCACCTCAGGCA | 51429 |
| rs534066653 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157751940 | ACAGAGCCGGGATCC[C/G]AGCACTTTGGGAGGC | 51429 |
| rs534075429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157815749 | TGCAGGGACATGGAT[A/G]AAGCTGGAAACCATC | 51429 |
| rs534078616 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157818542 | CAATGACACATGAAC[A/T]AGCAAAATGTCCTAT | 51429 |
| rs534084859 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157824198 | TGGTTTGCTTGTTTT[A/T]CGTTATTGTTTATGA | 51429 |
| rs534096152 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157927612 | TTTTAATCTGTTGAT[G/T]GATTTTAATCATGTA | 51429 |
| rs534107544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157917778 | TATTGTTTTGAGAAT[A/G]ATAACAAGGAAAAAA | 51429 |
| rs534109114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157856946 | AAATGATCTCATTCT[A/G]TTATTCCTTCATTTA | 51429 |
| rs534127520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157730321 | CTGAGGTCAGGAGTT[C/T]GAAGACCAGCCTGGC | 51429 |
| rs534145685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157793203 | GATCCACCCGCCTCG[A/G]CCTCCCAAAGCGCTC | 51429 |
| rs534163543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157843827 | ACAATTTCAAAGCAT[C/T]GTGAGTACAGAATTC | 51429 |
| rs534165780 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157911421 | ACTCGCAAGAGTCGA[G/T]AGAAACAGTTCAGGG | 51429 |
| rs534167319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157824969 | GGTTTATAGGCCGGG[C/T]GCGGTGGCTCACTCC | 51429 |
| rs534172823 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157924749 | CATCATGTAAATGAC[A/T]TCCGTATCTCTTTTA | 51429 |
| rs534180703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157748227 | GTATTAGATCTAACA[A/G]TATGAGGACTCTGTA | 51429 |
| rs534198301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157756042 | TGCCAGTAATCACAT[C/T]TGATGACAGTAAATG | 51429 |
| rs534204083 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157867067 | AATCCTCCCGCCTCA[A/G]TTTTTTCAGTAGCTG | 51429 |
| rs534215317 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157786640 | TTTTTATATACTAGC[A/T]GCAAACTATAAGACA | 51429 |
| rs534234098 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157741561 | ACTGCTGCTGCTGCT[A/G]TTATCAGGCAAAACC | 51429 |
| rs534238797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157850110 | GCAGGTGTGGAGGGG[C/T]GAGGGGAGGAGAGTG | 51429 |
| rs534239454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157917276 | TTGGTTTTATGTATT[C/T]TTATTTTTCTCTTTT | 51429 |
| rs534263478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157937160 | TTAGCTGAACTTCCT[C/T]CATGGTGGTATTATT | 51429 |
| rs534267848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157779279 | TCAGTTTCCTCTTCT[C/T]CCAAAGGAAGATAAT | 51429 |
| rs534290844 | in-del | -/TT | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157826907 | ATTATAGTTTATATA[-/TT]ATATATAAAATATAT | 51429 |
| rs534300471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157755412 | GAAGAGAATGCCTCC[A/G]GGTTAGAAAAACACC | 51429 |
| rs534304849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157843173 | TAGGTGGTGCCAGCA[A/G]TGGGAGGATGCTTAG | 51429 |
| rs534311548 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157926982 | CATGGTGCAGAGGGA[C/G]ATAGAGTGGGAGCTG | 51429 |
| rs534321525 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157840111 | GGCTGGTGCTTGGGG[A/T]GTCTTTGGATCTCGG | 51429 |
| rs534327941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157790149 | AACCTAGTCACATGG[C/T]CACAGGGAGTGCAAG | 51429 |
| rs534355194 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157744769 | TTTTTTTTTTGAGAC[A/G]GAGTCTTGCTCTATT | 51429 |
| rs534361707 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157831519 | TACCCTTATGCTGAG[G/T]TCCTTTTGGAGTCCC | 51429 |
| rs534371695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157772938 | ACACGGATAAGGCCA[C/T]CCAGGGAGAATGGTG | 51429 |
| rs534382997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157910896 | GGAGGCCGAGGCGGG[C/T]GGATCACGAGGTCAG | 51429 |
| rs534387060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157939764 | GAACTTGTGTTTGAG[A/G]TTATCCAAATTGAGA | 51429 |
| rs534393360 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157804291 | GCTTGTTTATGGTTT[C/T]TATGTCCTGGTTTTA | 51429 |
| rs534402644 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157871252 | CGGGTGTGGTAGTGC[C/G]TGCCTGTAATCCCAG | 51429 |
| rs534442899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157933737 | TCTCAACAGGGTGAG[A/G]AGATTTGTCCTAGAG | 51429 |
| rs534446287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157904201 | AGCACTTTGGGAGGC[C/T]GAGGCAGGCAGATCA | 51429 |
| rs534448968 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157819981 | TTCTCACCCCTGGAG[-/T]AATGGAAGTTCATGC | 51429 |
| rs534472315 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157827879 | TTTTTTTTTTTTTTA[A/T]CTCTTCGGTTCCAAT | 51429 |
| rs534480871 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157862142 | TTGATAGCAGTTCAC[C/T]GAAACCGAGGAACGT | 51429 |
| rs534481812 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157878041 | AGTTCATAAATGTAT[A/G/T]ACCTACTATGTAAGA | 51429 |
| rs534495761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157913775 | CTTTCGAGTCTGACT[A/G]CTTTCATTTAGCATA | 51429 |
| rs534520026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157742056 | CAGGAGGATATAACA[C/T]TATTTATTTCCTCTC | 51429 |
| rs534546188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157870696 | ATACACCCTGCAGAT[A/G]GTCTCACCTGCTCTC | 51429 |
| rs534546344 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157878618 | TTGTATTTTTGGTAG[A/G]GATGGGGTTTCACCA | 51429 |
| rs534559732 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157739715 | AATGCCCATCAATGA[C/T]AGACTGCATAAAGAA | 51429 |
| rs534560308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157927748 | TTTTTTTTTTTTGAG[A/G]CGGAGTCTTGCTCTG | 51429 |
| rs534560855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894442 | ACTTAACTCAGTTCC[A/G]GACAGATACAAGATT | 51429 |
| rs534563096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157820166 | ACAAACGCCACCACC[A/G]GGTGCAGTGGCTCAC | 51429 |
| rs534588714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157846948 | GCTACTTGGGAGGCT[A/G]AGGGATGAGAATCAC | 51429 |
| rs534612429 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157778529 | GGAGTAGTAAATCTT[C/G]AAGAATGGTTAGGAG | 51429 |
| rs534616870 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157880351 | GTCTTCAATCCACTT[A/G]CCCTTTTGTGTTCCA | 51429 |
| rs534624576 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887896 | GACAGTTGTGGAACC[A/C/G]GGATTTGAAGCCTGG | 51429 |
| rs534625713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157834481 | CCTCACAAGTAGCTT[A/G]GACTACAGCTGTGTG | 51429 |
| rs534627346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157920389 | CCACCATTGAACATG[A/G]CATCTCCCATCACTC | 51429 |
| rs534633189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157738616 | TCTGTGTCTTTTAAC[C/T]GGGGCAATTAGCCCA | 51429 |
| rs534649527 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | SNX9 | GRCh38.p7 | 6:157840443 | CTTTTCTTTCCTTTC[C/T]TTCCTTTCCTTCCTT | 51429 |
| rs534653590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157929157 | CGAGGGGAGAGTGTC[A/G]CTGTCAGTCACGGCT | 51429 |
| rs534654361 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157815142 | TGGTTCTCGTCACCA[C/T]AATAGAAGAGTTTTG | 51429 |
| rs534657307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157853039 | GCCCATGTATTTACC[A/G]TTCCTGGTGCTCTTC | 51429 |
| rs534673868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157717154 | ATAGCTCACTGAAGC[C/T]GCAAACTCCTGGCTC | 51429 |
| rs534676405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157757396 | TGTTACCGGGGACAC[A/G]CTCATTCACTCAACA | 51429 |
| rs534679569 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157727227 | AGGAAAGAAGGGAAT[C/T]TCTTGTAGTAACCAG | 51429 |
| rs534681051 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157860625 | GCACCGCATATAGAA[C/G]CTTTGATCTGGGTGA | 51429 |
| rs534689859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157854946 | TGACGGGATAATAGG[C/T]TCATGTTAAAAAAAA | 51429 |
| rs534701910 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157798926 | ATTAGTCAGTTCTCA[C/T]GCTGCTATAAAGAAT | 51429 |
| rs534709373 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157850410 | GTTGAGGGATGGTTT[C/T]TTCTTCCTTTTTAAG | 51429 |
| rs534745452 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157940247 | ACACCAGAGGCTTTG[A/C]ACTGCAGTCATCTGT | 51429 |
| rs534745929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157895642 | AAAAAAAAAAGTACC[A/G]AGCAAAAATAATACA | 51429 |
| rs534763053 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157726143 | AAGGAACTGTCCCAT[A/C]TCACCACACTCAGTG | 51429 |
| rs534763377 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157754283 | GTCTTTGTTTAAACT[A/G]TAAACTAAGTTTCTC | 51429 |
| rs534812636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157874645 | TCTTTTCAAGCTTAC[A/G]TGGAACATTCTCTAA | 51429 |
| rs534850886 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157764514 | AGTTTAATTACGTCA[C/T]ATTTCCACCTCAATT | 51429 |
| rs534895641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157727332 | TTGGGGTCATATGCC[C/T]ATGTGCAGTATCACA | 51429 |
| rs534941702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157855928 | GTTTTTTTGTATTTT[C/T]AGTAGAGACAGGGTT | 51429 |
| rs534950137 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157782950 | AAATAGATGAGAAAG[A/T]AAGAAATAAATATGA | 51429 |
| rs534961152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157719576 | TTCCTGGCACTGAGT[A/G]ACGATAACTCAATTA | 51429 |
| rs534981464 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157901004 | GGTGCCCCCATGTGT[C/G]TGTTTATAGGCTCTT | 51429 |
| rs534988658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157814117 | CTATAACCACTGGGC[A/G]AATGAATGCCTTCAA | 51429 |
| rs534996693 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157753549 | AGATTAAAAACAGCC[A/G]TGGTTAAGTCCAGAG | 51429 |
| rs535003841 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157788281 | TATGGATATTAATTT[C/T]TTTCAAGGGAAAAAG | 51429 |
| rs535019501 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157760071 | AGAGATGGGGTTTCA[C/T]CATGTTGGCCAGGAT | 51429 |
| rs535025020 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157805969 | ACATGCATCAATTTT[C/T]CCCGGCCACAGGCTG | 51429 |
| rs535031107 | in-del | -/ACTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157804246 | GGAGAGGCCTAAGGG[-/ACTT]ACTTGCCTGTGATGA | 51429 |
| rs535058476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157718744 | GTTTTTTTTTTTTCA[A/G]AGTCTTGTCCAATCC | 51429 |
| rs535058969 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157817341 | TTCAGCACTCAGCAC[A/T]CAGCAGTGGGTGGGC | 51429 |
| rs535085956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157868398 | GCTTATATAACTGGG[C/T]TTATTATGCCCTCCC | 51429 |
| rs535091706 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157767941 | CCTCAGAGTGGAGGC[A/T]CCTGGGGGGACAGCT | 51429 |
| rs535094788 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157721589 | CCTCGCTGCCTTTGT[A/G]TGGCCCGGCCTGTGT | 51429 |
| rs535096411 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157874022 | GAAGGTTTCCTGATG[C/G]CCTGTGAGTACAACT | 51429 |
| rs535148687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157729727 | GGGAGGCTGAGGCGG[A/G]TGGATCACCTGAGTT | 51429 |
| rs535149520 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157862905 | AAGTGACAAGATGTG[C/G]ACTGACAGTTTAATA | 51429 |
| rs535169645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157870559 | GACACTCTCACCTGC[C/T]CTCACACATATATGC | 51429 |
| rs535171190 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157869015 | AGAGGTACCCTGGAG[A/T]TACAAAGACAGGAAA | 51429 |
| rs535207697 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157784941 | ATCTTACCCAACTCT[C/T]AGGAAATAGAAAAGA | 51429 |
| rs535223418 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157929150 | GCACTGCCGAGGGGA[C/G]AGTGTCGCTGTCAGT | 51429 |
| rs535246181 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157762682 | AGTGTCCCGGAGCCC[A/G/T]CTGTGGCTAGGGAGG | 51429 |
| rs535282420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885463 | GTTAGATTTTTTTAT[A/G]TAAGAGAATATTATA | 51429 |
| rs535294387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157795607 | TTAAAGGTTAAGTGT[C/T]CTGATGTCTGGGGCT | 51429 |
| rs535301957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157759575 | TGGCGGGCGCCTGTA[A/G]TCCCAGCTACTCAAG | 51429 |
| rs535318317 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157858826 | CTCCCCTTTATAAAA[C/G]CATCAGATCTCATGA | 51429 |
| rs535326258 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157838609 | GCCATAGTGTGAAAA[G/T]TTTATGTAGAAGTGC | 51429 |
| rs535331485 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157799182 | CATGAGAACAGCCTG[G/T]GGGAGACGACCCCCA | 51429 |
| rs535347144 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | SNX9, LOC107986663 | GRCh38.p7 | 6:157715169 | ACATTTCCCCTCCCT[A/G]TGCCTTCCTCACGCT | 51429 |
| rs535353841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157935841 | CATTCTATTCCCAAT[A/G]GTTTTGAAAATGTTT | 51429 |
| rs535355597 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157943567 | CTCTTATGTGAGGAC[C/T]AGTGCTTTCTCTCTT | 51429 |
| rs535397325 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157832438 | TGCAGGGGCACAGTG[C/T]AGGCTCCTGGCACAG | 51429 |
| rs535414934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157721629 | GCAGGGAACCCTCTT[C/T]CCCACCGCGGCTCTC | 51429 |
| rs535415640 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157903780 | AAGGCAAGTTTCGTG[A/T]CCTGTTGGAACCTCA | 51429 |
| rs535415865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157938517 | TCTTCTTATTTTGTG[A/G]AGGTATTTCCTGTTC | 51429 |
| rs535436507 | snp | A/G | 1.65061e-05 | 0.00287277 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157942881 | GCGTGCTTTCTCCTG[A/G]CTTGGGGCAATGCAA | 51429 |
| rs535459031 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157918808 | CTTTTTTAACATCAC[A/G]GTGCACTTTAGATTA | 51429 |
| rs535477846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157773537 | TGGAACGGTTTAAAG[A/G]GCAGCAGCAATATAA | 51429 |
| rs535484925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157809872 | GAATTGGGAATGGAA[A/G]ATGGTACTGCCATTT | 51429 |
| rs535519874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157912339 | TTAGATTTTAATACA[C/T]TGTTTATTCTGAATC | 51429 |
| rs535531836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157878820 | ACTTCTGACTTATGA[C/T]GGATACAGGCTAATT | 51429 |
| rs535533328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885996 | TCATTAATTCTTAAA[C/T]CTAGCCCTCCTTCGA | 51429 |
| rs535537594 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157898808 | GGACCTCACTTGTAA[A/G]CCCAAAGCAGGGTGC | 51429 |
| rs535541953 | in-del | -/G | 0.116138 | 0.211142 | intron-variant | SNX9 | GRCh38.p7 | 6:157826830 | ATATATATTATATTT[-/G]TATATATATATTATA | 51429 |
| rs535541989 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157816471 | TACTGATGTGCCTGG[-/A]AAAAATCCTGAGAAA | 51429 |
| rs535578853 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157792379 | CTCTCGTCCTCGTGA[C/T]CTGCCCGCCTTGGCC | 51429 |
| rs535585905 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157780188 | TGAGTAAGCCTCCTG[C/T]TCCGTCCCTGCTTAC | 51429 |
| rs535586368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157767518 | TGTCCCTGCATTATC[A/G]CGAACCTTCCATGTG | 51429 |
| rs535591524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157879146 | CATATCTCTAAGGCC[C/T]AGCGGTTCTGAGTTC | 51429 |
| rs535591892 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157772897 | AAATGGAGATCATGG[C/G]GGAATAAGGGGTGAG | 51429 |
| rs535635941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157932407 | AATTGGCTAGGCTGC[C/T]GCACTAAGGACTTTT | 51429 |
| rs535659314 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157763058 | GCATATTCTCCTCTT[A/C]CAAGCTACACAGATT | 51429 |
| rs535688611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157899907 | AGTGTGTGTGTGTGC[A/G]CGTGTATATGTGCAA | 51429 |
| rs535693847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157803747 | GCATTTTGCTTGTAT[A/G]TGAATTTCTTCTGTT | 51429 |
| rs535702325 | in-del | -/T | 0.00953873 | 0.0683987 | intron-variant | SNX9 | GRCh38.p7 | 6:157874454 | ATAAAGGAATAGTGA[-/T]TTACAGATATTCTTG | 51429 |
| rs535713004 | snp | C/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157891495 | TGATTTCCTCCTTTT[C/G]GTGATCATGTCATGA | 51429 |
| rs535715144 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157855973 | AGGCTGCTCTTGAAC[A/G]CCTGACCTCAGATGA | 51429 |
| rs535720324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157716704 | ATTCTAAATTCAATG[C/T]CCTGGAAGATACTGA | 51429 |
| rs535722260 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157769061 | AAATAAATAAATAAA[-/T]AAATAAATAAATAAA | 51429 |
| rs535727182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157810437 | TAAAATCACTGAATT[A/G]TATTATAAATTACTC | 51429 |
| rs535736571 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157748160 | TCTGAATTTTATTAG[-/T]TTTTTCATTTTGTTT | 51429 |
| rs535746690 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157884493 | ACCTTCATTAACTCA[C/T]ATAAGTCTTATAATG | 51429 |
| rs535746891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157905445 | GGCTATGTTCTAGCT[A/G]TCCTCTAATTTCAGA | 51429 |
| rs535758097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157818686 | TCATGAGACACCAGG[A/G]ATCCTACAGGCTGGG | 51429 |
| rs535761149 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157715885 | AACAGTGAATTAGAG[C/T]AACCCTCATGACGAA | 51429 |
| rs535809121 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157825120 | GGGCGTGGTGGCGCG[C/T]GCCTGTAGCCCCAGC | 51429 |
| rs535809234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157832680 | CAGCAGGAAGAAGTG[C/T]CGAGCAAAAGGGGGA | 51429 |
| rs535826302 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SNX9 | GRCh38.p7 | 6:157746749 | TAAAATCAGGAAAGA[C/T]AGGCTGGGTGACAAG | 51429 |
| rs535829203 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157769309 | AGCCTGGCATCGATC[C/T]GACCAACAATCAACA | 51429 |
| rs535867711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157776348 | AAGAACTCCCACTTG[C/T]ATCACCCCAGGACAA | 51429 |
| rs535869122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157785017 | TTTGGGAGGCCGAGG[C/T]GGGCAGATCACGAGG | 51429 |
| rs535899036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157825817 | CTTTCCTCCCTTCCC[C/T]CATATGCACACTCCT | 51429 |
| rs535905213 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157932972 | CTGTTTTCTCCTTAA[C/G]TCATAACTGTTTCAG | 51429 |
| rs535905227 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157925386 | TGCTGGGATTCATAA[C/T]GTGTTGGGGGAAAAT | 51429 |
| rs535908487 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157818051 | TCAGGGTTCTCTAGA[C/G]GGGACAGAACTAATA | 51429 |
| rs535922636 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889657 | TGAAGGTAACAGAAC[A/G]TTGGCTGGAATAGAA | 51429 |
| rs535924377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157882006 | CAGCCTTCTATTATT[A/G]GAAGAAGATGCCATC | 51429 |
| rs535926092 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157928448 | TAGTTCTTTAAATGT[C/T]TGCATCAAGCCTGTA | 51429 |
| rs535939101 | in-del | -/T/TT/TTT | 0.220423 | 0.254959 | intron-variant | SNX9 | GRCh38.p7 | 6:157765345 | TTTGAAATATATTTG[-/T/TT/TTT]TTTTTTTTTGTTTGT | 51429 |
| rs535947835 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157864945 | AGGCAGGAGAATTGC[C/T]TGAATCCAGGAGGTG | 51429 |
| rs535969392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157839547 | ATAATTGAATGGATT[C/T]AGGTGTGAATTCCAT | 51429 |
| rs535971413 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157791566 | AAAAGCTGTGCCCAT[A/C]CTCCTCAACAAATAC | 51429 |
| rs535977273 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157784301 | AATAAAGGGAAAAAA[A/T]AATTTTTCAATATCA | 51429 |
| rs535981902 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157871459 | TGCATGTTCTCATTC[A/G]TAGGTGGGAATTGAA | 51429 |
| rs535984495 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157921266 | CACCTTGAGGTTGTC[A/G]TTATTCTTGTCACAA | 51429 |
| rs535987912 | in-del | -/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157794833 | TATATTTATATTGTC[-/T]TTTTTTTAAAAGACC | 51429 |
| rs536006217 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157874702 | AACATACCTCAACAT[G/T]TTTGAAAGAAATCAT | 51429 |
| rs536012889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157909072 | CCCACCTTGCCACTA[A/G]TAGTAAAACAATGAC | 51429 |
| rs536016055 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157862003 | GAGATGCTGGACAAA[G/T]GGATGATTCATGTCC | 51429 |
| rs536037485 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157724736 | CCTGAATTTGTCTAT[A/G]TAAATGATTCCAAAC | 51429 |
| rs536044217 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157772061 | GGGGGACTCAAAAGG[A/G]CAAAGAGGAAGAGTA | 51429 |
| rs536046381 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157860847 | TGCTCCCCTAGAATT[G/T]TACAGTCGCCTTTTG | 51429 |
| rs536046533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157852516 | TCAAATACTACAGCA[C/T]CTCACACGTAAGAAC | 51429 |
| rs536085769 | snp | C/T | 8.23934e-05 | 0.00641794 | intron-variant | SNX9 | GRCh38.p7 | 6:157909802 | TACTGTAAGTATCCA[C/T]GTTATCAAAAGCAGA | 51429 |
| rs536100387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157815656 | ATAGATAGCTTAGGC[A/G]TGAAATAAGAAGCAG | 51429 |
| rs536100809 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157725242 | TATCACGGGTTCTGA[A/T]CAGTTTGGTTGTGAT | 51429 |
| rs536103999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157776906 | GAGGAATCCACTCTT[C/T]ATCTGCAGAAGGGAA | 51429 |
| rs536104123 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157728574 | GCCCAGAAGCAATGT[C/T]ATCTTTTTCCCCCTC | 51429 |
| rs536120821 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157733995 | ACAAAAGTAAAAATG[A/G]TGATGAATAACAATA | 51429 |
| rs536127310 | in-del | -/AT | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157754071 | GGGTGGTGCCAGCTG[-/AT]CCATCAAGTGCAGGG | 51429 |
| rs536152575 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157908362 | ACAGTCCATGTGTTT[A/G]TTTTTTCATTCTCTT | 51429 |
| rs536157065 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157912900 | TTCTAATTATTTGCA[A/G]CTTGGTCTGAAAATT | 51429 |
| rs536167836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157915858 | TATGTAAGAATTTCA[C/T]TGGAGAGTTGTATTG | 51429 |
| rs536186000 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157944402 | TGTTTATGCTATAGC[C/T]ATTTAATATATGTAC | 51429 |
| rs536211392 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157897665 | GGAGCCCACCGCCCA[C/T]CGCCACACCCGGCTG | 51429 |
| rs536237303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157929959 | GTAAATAAAGTTTTA[C/T]TGGAACACACCCATG | 51429 |
| rs536241098 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157937006 | TTTAATAACATAGCT[A/G]TTAAAGTTATAATTC | 51429 |
| rs536244419 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157835602 | TGAATTGTAATCGCT[A/G]TAATCTCCAAGTGTC | 51429 |
| rs536245425 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157734641 | ATTTATGGCTCTTTG[A/T]TAAAATACTATTTGA | 51429 |
| rs536269298 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157780774 | TTCTTTCTTCTTTCT[C/T]TCAATTTTTTGCAAA | 51429 |
| rs536283303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157836644 | CGCCCAGGCTGGAGT[A/G]CAGTGGCGCGATCTC | 51429 |
| rs536306820 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157720322 | TTCCCTTTCCTAAGG[G/T]GTTTCAGATTTTCAT | 51429 |
| rs536309587 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157732893 | TTTCTGCCATCCTTG[C/T]CCCCGCCCTTGGCAA | 51429 |
| rs536311492 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157935743 | TGAGATGCTGATGTC[C/T]GGTGAAAGCGGGTCG | 51429 |
| rs536321117 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157766340 | ATGGAACAAAGAAAT[A/C]TTTCCTATTGCTGGA | 51429 |
| rs536326431 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157838241 | TGGTCTTGAACTCCT[A/G]GGCTCAAGCAGTCTG | 51429 |
| rs536364194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157746185 | TTAGGACTAGTCCAG[C/T]GGACCAATGGGAATA | 51429 |
| rs536379619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157942513 | TCTGAGGAAAAGCAG[A/G]TGGTCTGGAAGCGCC | 51429 |
| rs536401752 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157741521 | TAAATGATCACTGGC[A/T]GCACACTGAGCCACA | 51429 |
| rs536403059 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157800695 | ATAGCTATTAAATGT[A/G]TATTACTTTTGTTAC | 51429 |
| rs536428445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157924655 | TTATTTAGAGGTGGT[A/G]CCATTCTTGGAAAGT | 51429 |
| rs536431367 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157727902 | AAATAGAAACTCTTC[A/G]TGAGATGGACAAAAG | 51429 |
| rs536431649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157756273 | CAAAAATTGGCTGGG[C/T]GTGGTGGCAAGTGCC | 51429 |
| rs536433238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157765819 | TTATTCACAGGGGAG[C/T]TTTGGAAACAAGTAG | 51429 |
| rs536433312 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157752130 | CAGGAGGCGGAGGTT[A/G]CAGTGAGCCGAGATT | 51429 |
| rs536441391 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157864246 | TAAACCCACTCCCAC[A/G]AGCCCTTTTTGTAGC | 51429 |
| rs536454546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157735850 | ACACACCTATAATTC[C/T]AGCTATTTGGAAGGC | 51429 |
| rs536470529 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157770515 | TTTATTGGCCGGGTG[C/T]GGTGGCTCACGCTTG | 51429 |
| rs536473347 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157830760 | GCTACTTTATAGGTG[A/G]GTGCAGCTCTAGAAA | 51429 |
| rs536474855 | in-del | -/TTTGTTTG | 0.00677013 | 0.0577861 | intron-variant | SNX9 | GRCh38.p7 | 6:157836109 | GCTAATATTTAATTT[-/TTTGTTTG]TTTGTTTGTTTGTTT | 51429 |
| rs536493304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157917024 | TCACCACTGAAATCA[C/T]CTGGACCTGGAGTGT | 51429 |
| rs536497814 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157929901 | TACATCAGGAGTCAG[A/T]AAACCATGGTCCGAG | 51429 |
| rs536507472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157843101 | TAATTTCCTCAATTA[C/T]AATTTTGCAAAGGTG | 51429 |
| rs536521526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157734478 | CACCTAAAGACAAGG[A/G]CCTTCACAACATTAG | 51429 |
| rs536535955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157793553 | AATATATATATAAGC[C/T]AAATACTAATTTTCT | 51429 |
| rs536561344 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157907880 | ACAGTTGCTGCTCTC[A/G]GCCCACTCACTGAGG | 51429 |
| rs536577590 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157797011 | TCCTAGCTGTGCTCC[C/T]ACTGTGTAATCTCTG | 51429 |
| rs536596472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157771768 | ACAGTGGCATCATCT[C/T]GGCTCACTGCAAACT | 51429 |
| rs536600783 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890265 | CGTGTCCGTCTCCCC[C/G/T]ACCCCTCGTGGCCAT | 51429 |
| rs536616237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157800742 | CATTGTGAAACTGCA[C/T]ACTGTGGTGACTCAT | 51429 |
| rs536640806 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157845407 | CGAGCCACCGTGCCC[A/G]GCCCCATTTGTCTTA | 51429 |
| rs536643453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157754961 | TTTCTTGATGATATG[C/T]TAAACAAGGGGTGAA | 51429 |
| rs536644393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157933107 | ACCCAGGCAACATAA[A/G]GAGACCCCATCTCTA | 51429 |
| rs536646282 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157939587 | AGAAGAGAATGAAGC[A/G]CATTTGCAGGCTTTT | 51429 |
| rs536648150 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157835299 | ATTACAGGCGTGAGT[-/C]ACCATGCCCAGCCAA | 51429 |
| rs536654130 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157793152 | ACGGGGTTTCACCAC[A/G/T]TTGGCCAGGCTGGTC | 51429 |
| rs536659751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157883259 | CTCGCACACTTATAC[A/G]GTATAGTGTAACCAT | 51429 |
| rs536674186 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157755284 | TGTATTCAAGATGGA[A/G]TTGCTCTGGTTCGCA | 51429 |
| rs536683136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157747582 | ATTAACTACTCGTTC[A/G]AGGCATATTGCAATA | 51429 |
| rs536683668 | snp | G/T | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894291 | ATTTTTGTATTTTTA[G/T]TAGAGATGGGGTTTC | 51429 |
| rs536696610 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157856830 | TTTTTTTTTCAAGTA[C/T]ATTTCATAAGCAGGA | 51429 |
| rs536697688 | in-del | -/T | 0.00835141 | 0.0640778 | intron-variant | SNX9 | GRCh38.p7 | 6:157786211 | CTACATCTGGCTAAA[-/T]TTTTTTTAAAATTGT | 51429 |
| rs536709185 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157936513 | GACCCTATCTCAGAA[G/T]AAAAAAAGACATCTA | 51429 |
| rs536710735 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157716014 | GAAAATAGCCCCACC[C/G]AGTCAAAGAACTAGT | 51429 |
| rs536714512 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157841209 | TCATGGTTCCATTAA[A/G]TGATTATTTTTAATA | 51429 |
| rs536717743 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157944205 | CTGCTTTCATTTTTC[A/T]GACCTAATAATTACG | 51429 |
| rs536719882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157942065 | TCCAGGTATGGTATA[A/G]TGACATTGTAATTCA | 51429 |
| rs536725851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157811482 | AAAAAATAAAAAAGC[A/G]TTATTGGAGTAGAGG | 51429 |
| rs536771796 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157716558 | GGGAGACCAGCAAGA[G/T]AGAAGTGGTCAAGGT | 51429 |
| rs536781809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157852443 | TCCCTTCCTCCTCTC[A/G]CTACCATGGTCACTC | 51429 |
| rs536811979 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157851268 | TCAAAAAAAAAAAAA[-/C]ACCCTAAAATAAATA | 51429 |
| rs536837681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157833527 | TTCCAGGGGAAAAAA[A/G]GAGTATGTTTTAAAA | 51429 |
| rs536840728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157919483 | CTACCTTAAATCTTA[C/T]GTTGAGCCTTATCTG | 51429 |
| rs536844182 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157877916 | CTTCCTGAGTGTCGT[A/G]TTTTTCTTTAAGTAT | 51429 |
| rs536857182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157873244 | TTTATGAATTATCAA[C/T]TTACAAGAAGTCAGC | 51429 |
| rs536859525 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157870275 | ACATCCCCACGCTCA[G/T]GCTCTCACATATGCA | 51429 |
| rs536874906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157834295 | ACCTCAACATCCTGA[A/G]TAAGCTGACACCACA | 51429 |
| rs536875488 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | SNX9 | GRCh38.p7 | 6:157826853 | ATATTATATTTTATA[A/T]ATAAATATATATTAT | 51429 |
| rs536876583 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-5-prime, intron-variant | SNX9 | GRCh38.p7 | 6:157823341 | CCCAGCCGGAGCCGC[C/T]GCCCTCGCCCTTGCC | 51429 |
| rs536894565 | snp | C/T | 0.000362911 | 0.0134656 | intron-variant | SNX9 | GRCh38.p7 | 6:157910072 | CAAATAGAAAGACTC[C/T]AGTCAGATTATCTTC | 51429 |
| rs536904938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157933563 | CTTTTAGACCAGAAG[C/T]GGGCTTTGAGGTCTA | 51429 |
| rs536924260 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157883620 | CATCATCACCTTATC[C/T]TTAAGTTATGTATTT | 51429 |
| rs536937013 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157895896 | GGTCCCAAAACAAAC[C/T]GATTTTTTCTCGAGA | 51429 |
| rs536950884 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157840108 | TCAGGCTGGTGCTTG[C/G]GGTGTCTTTGGATCT | 51429 |
| rs536961447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157744190 | TTTATATGATCATAA[C/T]GCTCCCGGCCGGCCC | 51429 |
| rs536965425 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157926823 | TAGGGTGTTTCTGTT[C/T]GCTGTTTTTATATAG | 51429 |
| rs536974408 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157923959 | TTTAAAACATGTCCC[A/T]GGCTGGGTGTGGCGG | 51429 |
| rs537007879 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157899874 | CTTAACATATCCCTC[A/C]CCTCACATGATTACC | 51429 |
| rs537028988 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157925238 | TCTGAATCAACAACA[A/G]ATGTGTAGAAAAGTA | 51429 |
| rs537032516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157732937 | CTCTGCTGCTGTTTG[A/G]CTTTTTCAGATTCTA | 51429 |
| rs537033824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157725427 | TCAGGGACCTTAATT[A/G]TGGATTAAGCTGATT | 51429 |
| rs537047788 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157852998 | ATGGTGAGTTTTTTT[G/T]TTTGTTTGTTTGTTT | 51429 |
| rs537058747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157862120 | ATTTAATATTTTCCA[A/G]CTGCATTTGATAGCA | 51429 |
| rs537061633 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893985 | GATATGTGATGAAGG[A/C/T]GGCATTTCAAATCAT | 51429 |
| rs537063315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886178 | GTCAGGTCTAACCAT[A/G]TCATCCAAACAAGCG | 51429 |
| rs537107877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157762620 | ACAAAGAACAGCTAA[C/T]ATTTAGAGAAGTGAC | 51429 |
| rs537111509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157774692 | CAACCCCTCACCTCC[A/G]AAGCCTTCACATCTG | 51429 |
| rs537112737 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157867289 | TAACTTTTTTAGGGT[C/T]GATCTCTAAATGCAA | 51429 |
| rs537118053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157859817 | AGAAACTCTTTATGT[A/G]TCAGAAGATTAACAC | 51429 |
| rs537118885 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157732376 | ATTTGAAGAGGTTCT[A/T]GTTTCTTTTTTTGAC | 51429 |
| rs537132733 | in-del | -/TGTG | 0.0126979 | 0.078662 | intron-variant | SNX9 | GRCh38.p7 | 6:157787462 | CTCTCTCTGTGTATA[-/TGTG]TGTGTGTGTGTGTGT | 51429 |
| rs537203568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157744702 | GATGACAGCATTTTC[C/T]CGGTTCCCTCTGGAC | 51429 |
| rs537213174 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157798348 | TAACTGGTTTGTAAC[A/C]TTTGAAAATGTCAAG | 51429 |
| rs537240573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157759517 | ATGGCCAATATGGTG[A/G]AACCCTGTCTCTAGT | 51429 |
| rs537258860 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157812214 | ACCCGATTCCATTCA[C/T]TAAAAACATTTCAAT | 51429 |
| rs537267041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157782277 | TGAGTTCTCCTGTGC[A/G]TATGCACACTGACCT | 51429 |
| rs537291082 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157913087 | AATGGGGAGTTCATC[A/G]TATCCCAGGTCCAGA | 51429 |
| rs537295554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157920213 | TACTTGTATGTACAG[C/T]CTCAGAGTTGACCAG | 51429 |
| rs537299002 | snp | A/G | | | utr-variant-5-prime | SNX9 | GRCh38.p7 | 6:157716107 | GCTGGGTGGACCCTC[A/G]CCCACCAGGAATAGC | 51429 |
| rs537311157 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157784527 | GTACCACCACACCCA[C/G]CTAATTTTTGTATTT | 51429 |
| rs537311645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157846072 | TGCAGGTGTCTCTTA[C/T]GGCCCTCCTGATGAG | 51429 |
| rs537312916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157764372 | TTCTCCCAATCTACC[C/T]GAAACTGGCTCTCTG | 51429 |
| rs537318968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157854110 | GTGTGGGAGATGGGT[A/G]CTCTCAACTGGGAGT | 51429 |
| rs537319409 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157917930 | ACTATCTGGCCATTT[C/T]CTGAATTTTTTTCTT | 51429 |
| rs537330501 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157789384 | TAGATTCAGGAGCCA[C/T]ATGGTCTCTGTTAAA | 51429 |
| rs537335470 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894666 | AGGAATTATGGGAGA[G/T]AAATACTTTTTAAAA | 51429 |
| rs537346595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157757081 | TTTACCAAGATGGTG[C/T]TGCCTCTCTAGTAAA | 51429 |
| rs537352114 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157758927 | CACAGATGAGACCTG[A/C]GTTCAACAGGGAGAC | 51429 |
| rs537368249 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157899183 | TCAGAATAGTAGCTA[A/C]TGATGCTGCTTAATT | 51429 |
| rs537368870 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157790069 | AGGCAGGGAGGACGG[A/G]TGCATCCACTCCCTC | 51429 |
| rs537369876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157718457 | TGAGCTCAGATCCTA[C/T]ATCCCTCTTTCTCTA | 51429 |
| rs537386879 | in-del | -/ATATA | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157827177 | ATATAATATATAAAC[-/ATATA]TTATAGTTTATATAA | 51429 |
| rs537398607 | snp | C/G | 0.00358779 | 0.0422022 | utr-variant-5-prime, intron-variant | SNX9 | GRCh38.p7 | 6:157823259 | GCGGGAGTAGCCGAG[C/G]GCCCAGCGGCTGGGC | 51429 |
| rs537413040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157906875 | CTATCTTCTGATCCT[A/G]TTGACTTAACCCTGT | 51429 |
| rs537418810 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157772521 | GGACCAGCACAGCCC[A/G]CTGGCAGCGCCTGAA | 51429 |
| rs537460436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157864920 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 51429 |
| rs537464601 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157803113 | GTCTTTCGTGTGTGC[A/G]TGTAGCAAGGATGGT | 51429 |
| rs537474299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157907642 | GTGGTACAGAGCTAA[A/G]GGTTCCAGCCTTTCA | 51429 |
| rs537480463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157812968 | GATCAGAGAGGATAT[A/G]GTGACTTTGTCAGTT | 51429 |
| rs537497055 | in-del | -/TC | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890928 | TTGCCCATTCCTCCA[-/TC]TCTCCTGTGCCTGTC | 51429 |
| rs537500494 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157726028 | TCCCTCTGTTTCCCA[C/G/T]GCTCACTTGCTCACA | 51429 |
| rs537523248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157741489 | TTTTTAACAATGGCC[C/T]CCAGGTGATTCTGAT | 51429 |
| rs537532961 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157852766 | ATTTGTAGAGACAGG[A/G]TCTCTCCACGGTGCC | 51429 |
| rs537537088 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157873970 | GAGCGAAGGTTCTTG[G/T]TAAGCTTGTCTTTCA | 51429 |
| rs537549954 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157913715 | GTGTTCATAATTCTG[C/T]GTTTTCTAGGATGTC | 51429 |
| rs537561442 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157830161 | AGATCTAATCATATT[C/G]TACTGTGTCTTTGCT | 51429 |
| rs537569879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157827767 | TAGCTGTAATTTCTA[C/T]GTCAAAGTTAACCTT | 51429 |
| rs537591640 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157775214 | AAATACAAAATTAGC[G/T]GGGCGTGGTGGCACA | 51429 |
| rs537593710 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157828802 | TTAATGCGTCTAAGC[A/G]TCACTTCCCCGGGAA | 51429 |
| rs537594251 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157870237 | GCACACACATCCCCT[C/T]AGACACTCTCACCTG | 51429 |
| rs537605111 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157805881 | TGTTGAGTGCCTATC[C/G]TCTGTCAGGCACTAG | 51429 |
| rs537606227 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157895610 | TACCTTGCAGAATGT[C/T]TTATGCTGTTAAGAG | 51429 |
| rs537606532 | in-del | -/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157791745 | GCTCTTGCATTGCAC[-/G]GGGGGTAATGATTGT | 51429 |
| rs537611998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157898317 | TTCAAACGCTGGGTT[A/G]GTAAAGTAAAAGCAG | 51429 |
| rs537634946 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157765682 | GTTTTGTTTTATCAT[A/T]TGAGCGTAGTTTAGT | 51429 |
| rs537640416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157850831 | GGCTGCCAGGGGCTG[A/G]GCCTGTGCTGGGGTG | 51429 |
| rs537643776 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157941220 | AGTTGCAAGGCCCCA[A/G]GAAGTTCCTTATTGT | 51429 |
| rs537651070 | snp | A/G | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157847672 | TTCCACGTGGGCCCA[A/G]GAAGGAGGGAGGAAG | 51429 |
| rs537668505 | in-del | -/AGC | 0.0154538 | 0.0865337 | intron-variant | SNX9 | GRCh38.p7 | 6:157793075 | TTCAGCCTCCCTAGT[-/AGC]AGGGATTACAGGCAT | 51429 |
| rs537679950 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157753215 | AAGTGTTCTTGCCAT[A/G]GTTTTCTTTTTAGTG | 51429 |
| rs537710067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157767500 | TCTAGCAGCCATGAA[A/G]TCTGTCCCTGCATTA | 51429 |
| rs537710927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157717933 | ATGAACCCAAGAGGT[A/G]ATCCCTCACCCCTCC | 51429 |
| rs537716246 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157865392 | AGCAGAATTCTGTCC[A/T]CTTTTGCAGCCATGT | 51429 |
| rs537717398 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157804935 | GGGTGCCCCAGAAGC[A/C]GGGAGGGAGCCAGGT | 51429 |
| rs537755157 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157767892 | ATACTGTGAGGCCCT[C/G]GGAGGGTGCAATGGG | 51429 |
| rs537761379 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157784367 | GTTATCAAAAGGAAT[-/T]TTTTTTTTTTTTTTT | 51429 |
| rs537780610 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157941074 | TTGTATTCTTTAATC[C/G]TAAGTAATAAACCAA | 51429 |
| rs537793553 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157837796 | GGTGTCTAAATAAGA[A/G]AAGGGCAGCAGATCG | 51429 |
| rs537794955 | snp | A/C | | | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157715821 | TGTGCAAACCAAGGA[A/C]TGAAGAAATCTTGCA | 51429 |
| rs537812106 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157735665 | GACTGCTCCATCAAG[A/G]CCACCAAAATCCCAC | 51429 |
| rs537813541 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157858474 | TGATCCGCCTGTTTC[A/G]ACTTCCCAAAGTGCT | 51429 |
| rs537871474 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157751127 | AAGAGGTTTCATTGG[A/G]CTTACAGTTCCACAT | 51429 |
| rs537873672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157878800 | AATATTAAATTAGCA[A/G]AAATACTTCTGACTT | 51429 |
| rs537881550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157831636 | TGTGGAGTCTCCCAG[C/T]GGGAAATCCTGCCTC | 51429 |
| rs537899105 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157777708 | CATCCAGTGAATTCC[G/T]CCTGCTGGTGCTGTT | 51429 |
| rs537947596 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157856074 | TTTTATCTTGTTTAT[C/G]TTGGCTGTTGCCAGG | 51429 |
| rs537949433 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157916292 | ACCCGCCTCGGCCTC[C/G]CAAAGTGCTGGGATT | 51429 |
| rs537949569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157881462 | AGTGAAAGGAAGAGT[C/T]GCATTTCTCTCACTT | 51429 |
| rs537952554 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157794841 | ATATTGTCTTTTTTT[A/C]AAAGACCAGGAATAT | 51429 |
| rs537979505 | snp | C/T | 1.6489e-05 | 0.00287128 | missense | SNX9 | GRCh38.p7 | 6:157932246 | TGCAGAGTTTGGCCA[C/T]AGTGTTCAGTTCCAG | 51429 |
| rs537983017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157772284 | GTCCCCCAAAAGATA[C/T]GTTCAAGTCCTAATG | 51429 |
| rs537985452 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157787584 | CAGCAGCTCAGAAAA[G/T]CTCAGGGCATCATTA | 51429 |
| rs538004762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157818085 | TATATACACAAACAC[A/G]CACACACACACACAC | 51429 |
| rs538020994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157912133 | TCCTTATTGCTTTCA[A/G]TCACAGTTTTCTCTT | 51429 |
| rs538022596 | snp | G/T | | | downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157945521 | ACTTCTGTCATGGGC[G/T]TCAGTCCCAGGGAGA | 51429 |
| rs538036834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157937741 | TCTGTACATCACCTC[A/G]GGCATGAGTTGTGAG | 51429 |
| rs538086778 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157810684 | CCTTGATGTTGGGTT[G/T]TTTTTTTTTCTGTCT | 51429 |
| rs538091302 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157818556 | CTAGCAAAATGTCCT[A/G]TATCCACTGTTACTT | 51429 |
| rs538101264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157780122 | AGGTCCCGCCTGGCT[C/T]TCCTGCCTGGCTCTC | 51429 |
| rs538115261 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157730744 | TTCCAGGTTCAAGCA[A/G]TTCTCCTGCCTCAGC | 51429 |
| rs538118069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157857770 | TATTTGTATTTTTAT[C/T]AGAATTATTGAAGGA | 51429 |
| rs538144024 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157862428 | AGAAATATTACCTAC[C/T]CTTTATGCAAAACTT | 51429 |
| rs538155396 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886314 | AAAAAAATAACAAAA[C/G]CAGAAACTACTATTT | 51429 |
| rs538156471 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157865077 | AGGCATGGTGGCTCA[C/T]GCCTGTAATCCCACA | 51429 |
| rs538174805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157825061 | GAGACAAGCCTGGCC[A/G]ATATGGTGAAACCCT | 51429 |
| rs538175880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157850194 | GGTTGAGGGCCTAGC[A/G]TGGTGATTGGATTTA | 51429 |
| rs538176583 | snp | A/G | 3.29957e-05 | 0.00406162 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157942842 | CCAGTGATGTAGGAC[A/G]GAACGGGCCTTGAAG | 51429 |
| rs538184321 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157811021 | GCTACAGTTAACTAC[A/G]ATAGCATCACTGCAC | 51429 |
| rs538190247 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157749932 | AGGAATAAACTTAAC[A/T]AAGGAGGTGGAAGAC | 51429 |
| rs538194673 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157773482 | CTTGTGCACAAGTAA[A/C/G]AGGTTCAGCGTAAGT | 51429 |
| rs538198189 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157878165 | GCAGAGTTGCTGGTG[G/T]CAAGGCAGTGTTGCT | 51429 |
| rs538207991 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888800 | GTGATGTGGGATGTG[A/G]AATATGTAGGAACTG | 51429 |
| rs538213377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157880990 | TAATTATAGTTATCT[C/T]ATATACCACTGCTTC | 51429 |
| rs538234455 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157838506 | AGATAGCTCAGTATT[G/T]GGAGTCAGAAATGAG | 51429 |
| rs538253753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157753144 | CTTCTTTCTATATAG[A/G]CAAAGTAACAGTCTG | 51429 |
| rs538270170 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157783044 | CATTTTAAATATAGA[A/C]ACACAAAAAGGATAA | 51429 |
| rs538317025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157934566 | AAGGTCAGAAAGACT[A/G]TAAGAATGTTAGTTG | 51429 |
| rs538343251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157895379 | TTTAGAGCCCTAGTA[A/G]TTTAAAAAGTTGCTC | 51429 |
| rs538345028 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157798230 | GAGGGCGCAATGAGA[C/G]GAACTCACCATGATT | 51429 |
| rs538351566 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887990 | TGGAAGCGCATCAGT[C/G]AGTTACCTCTTCTCA | 51429 |
| rs538360319 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157905657 | AAACAAGCACATATG[C/G]TGATGAGCAGGACAG | 51429 |
| rs538360684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157924759 | ATGACTTCCGTATCT[C/T]TTTTACTAAACTAAT | 51429 |
| rs538363007 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157844423 | GGCCACAAGATCAGA[A/T]GCCCAGTTTATTGAT | 51429 |
| rs538378070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157927757 | TTTGAGACGGAGTCT[C/T]GCTCTGTCACCCAGG | 51429 |
| rs538381729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157790850 | TCCTTTGTCTTTCTG[A/G]TTCTCTGTTCTCTCC | 51429 |
| rs538389174 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157825725 | GAAGACCCTTCCTTT[G/T]TTTTCTGACATGCTG | 51429 |
| rs538390184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157732138 | GGAGGCAGGGAGGGC[A/G]GCCCCTTAGTAGTTC | 51429 |
| rs538404611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157820853 | AGCTAATTTTTGTAT[C/T]TTTAGTAGAGACGGG | 51429 |
| rs538405265 | in-del | -/A | 0.324619 | 0.238604 | intron-variant | SNX9 | GRCh38.p7 | 6:157854954 | TAATAGGTTCATGTT[-/A]AAAAAAAAAAAAAAA | 51429 |
| rs538412889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157774020 | ATCCCATGAAGAAAG[C/T]GTCTGGACTGAACAG | 51429 |
| rs538436771 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157797570 | ACCCATTCACAATGT[A/G]CACACCTAGAGTCTA | 51429 |
| rs538444341 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840740 | ATATGAGGAATACCC[C/T]AGTCAAATCAGCTGG | 51429 |
| rs538450860 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157859103 | TCCGCCATTACTGTA[C/G]ATGATGTCTTTTTCC | 51429 |
| rs538462659 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157862997 | TCAAGTTTGTCCTTC[A/G]AACAGGACACTGTTT | 51429 |
| rs538472747 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157734761 | TCGCTGGTTTTTCCC[G/T]TTTTAATCTGGCTTT | 51429 |
| rs538480129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157731519 | TTTCTTTTCCTTGGT[C/T]CTTACATGAGATTGG | 51429 |
| rs538488692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157892181 | AGCCCAGGAGCTGAA[C/T]AGGTTTTACCGTGAC | 51429 |
| rs538491642 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821341 | GATGCATTGTTGAAC[A/G]GCTGCAGAGAGAGCT | 51429 |
| rs538498109 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157921203 | GTTTTCATGTTGAGA[A/T]AAGATTTAATTTTTT | 51429 |
| rs538503694 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157908253 | TACTTTTTCAAGTCT[A/G]CAAGAATAAAACCTG | 51429 |
| rs538538888 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889156 | GTCAGAGACATCAGG[C/T]GCAGTGGCTCACGCC | 51429 |
| rs538561590 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157921894 | GTTGGCTCAAGATGG[G/T]CAGGGGCAGGGTGAG | 51429 |
| rs538561927 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157914438 | GCAAATAACTTGTCG[A/C]AGCTGTGGCTTGGCT | 51429 |
| rs538574572 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157872270 | GTTACAATTTTTCCT[G/T]TGATCATAGATTGAA | 51429 |
| rs538576983 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157911531 | TTCCTGGACACTTCC[C/T]GAGTGCCTCTCATCT | 51429 |
| rs538618839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157928397 | TGTATAGGCAGAAAG[A/G]AAGCGAAGTTAAAAT | 51429 |
| rs538626107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157719635 | AGCGAAGATAGTGCT[A/G]TGACAGCAGTCGCGA | 51429 |
| rs538643203 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157774196 | GGCAGTGAGGAAGGG[A/T]TTGGGAAAGAGACTT | 51429 |
| rs538651707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157881723 | AACAGGCCACAACAT[C/T]CCCTTAAGCCAAAGC | 51429 |
| rs538652814 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157856663 | TACCTCACTCCCAAC[C/G]CTTATCCCCTACTTG | 51429 |
| rs538659998 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157835117 | TCCTGGGTTCAAGCA[G/T]TTCTCCTGCCTCAGC | 51429 |
| rs538673364 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | SNX9 | GRCh38.p7 | 6:157746132 | TGCAGATAGAACTCC[A/C]GGAATCAAATGTCCT | 51429 |
| rs538684721 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157760178 | GCCCGGGCCATCAAG[G/T]TTATTTACATCTGCG | 51429 |
| rs538693687 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157847007 | CAGGTAGCACTACTA[C/T]ACACCAGCCTGGGCA | 51429 |
| rs538720358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157727805 | TGTGTAGCTGGGGTG[C/T]TCTGCAGGCCTGTTT | 51429 |
| rs538733261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157814990 | CTGGCCCTGGGGTTG[A/G]TGTGCTGGAGTTTGA | 51429 |
| rs538741309 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157752678 | TCCATTGCCCAGGGA[C/G]GAACATGAGATAGAT | 51429 |
| rs538757245 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157847588 | GGACTAAAGTGGCAA[C/G]CAGGAATGTGGGGAG | 51429 |
| rs538783193 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157941622 | GCCTCCGCTGGCGGC[C/G]TTGCTGCCTACCCAG | 51429 |
| rs538797375 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157747382 | ATCTCTTGCAGGAAT[A/C]GTTCACATTTTTTAA | 51429 |
| rs538828923 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157727385 | TAATTTCGTTTCAAC[A/T]AGAAGATCAGAGGCC | 51429 |
| rs538840268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157836548 | ATCACACAGAGTTTC[C/T]GATTCAGGAGGTCTG | 51429 |
| rs538842902 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157930422 | TGACTCAGGAACAAA[A/C]AGCAAAGTTGACGTT | 51429 |
| rs538843767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157869133 | TGTCTGTGCTGTAGA[A/G]CATGTTGGATCCCAC | 51429 |
| rs538879291 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157784054 | TAAATGAGTAGAGAA[A/C]AAAATTACAACTTTA | 51429 |
| rs538959757 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157739819 | TGGATGAAGCTGAAA[A/G]CCATCATTTTCAGCA | 51429 |
| rs538962395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157747017 | CATGCACAGTTCCCG[A/G]TAGGATTCAAGCTCC | 51429 |
| rs538965048 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157776223 | TAATTGGGAAGCACA[C/G]GGGCGACAGGAGCTA | 51429 |
| rs538966579 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157842419 | CTGCCCAATGGGTTC[A/G]CCATCACCACTGCCT | 51429 |
| rs538978253 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157754507 | GAAGCAGTTGGGTGG[A/C]TGCATTTTTTGGATG | 51429 |
| rs538979512 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157754930 | GAGGGCTGCTGGTTG[C/T]CCATTTTTATGGTTG | 51429 |
| rs539002658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157896587 | TTGTTGCTGTTTTCA[A/G]AGTTCCTAAGCAAAT | 51429 |
| rs539011914 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157760095 | CCAGGATGGTCTCAA[A/T]CTCCTGACCTCGTGA | 51429 |
| rs539032888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157810597 | GTTCCCTTAACTCTT[C/T]GGTTATTGCATTGTA | 51429 |
| rs539039920 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157851808 | TGGCCAAGCTGGTCT[G/T]GAACTTCTGACCTCA | 51429 |
| rs539045405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157909247 | AAAACTTGAGGACAA[C/T]TTGGTATTGTTGAAA | 51429 |
| rs539047262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157762489 | AGAAGTTTAGTATCA[C/T]GTATATTTAATATGC | 51429 |
| rs539048019 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157944086 | ATAAAGCAAAACAGG[A/G]CCTTGGCACACCGTC | 51429 |
| rs539064269 | snp | A/G | 0.0001271 | 0.00797081 | intron-variant | SNX9 | GRCh38.p7 | 6:157897050 | CATGGCTGAGTGGGA[A/G]AGACAGGGAAGACCG | 51429 |
| rs539088794 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157715946 | GACCCAGGCTCTGCA[A/G]GGAGAAGCCTGGCCT | 51429 |
| rs539103633 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157863507 | CAATATATATTGAAT[A/G]TATAGTTTGGAGTTA | 51429 |
| rs539109737 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157879400 | TGGGTAATGTTATCT[C/T]TCTTGTGTTTCAGTG | 51429 |
| rs539110847 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157722832 | ATATGGTGAAACCCC[C/G]TCTCTACTGAAAATA | 51429 |
| rs539122366 | snp | C/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893573 | TGGGTAATTTTCTTG[C/G]AATTATATTTTTTTC | 51429 |
| rs539127040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157866200 | TCTGGACCCTGTCTC[A/G]AGGATCCTCTTGAGG | 51429 |
| rs539128555 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157901805 | AAAATTGATTTGCCC[A/C]GTAGGTAGTTACTGT | 51429 |
| rs539134132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157817844 | CGTGCCACTGCACTC[C/T]AGCCTGGGCAACAGA | 51429 |
| rs539139827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157765673 | AATGTATTTGTTTTG[C/T]TTTATCATTTGAGCG | 51429 |
| rs539141853 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157871416 | GTAGAAAAAGATTAT[A/G]TAGTAATTTTGTATA | 51429 |
| rs539157485 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157855995 | CTCAGATGATCCACC[A/C]GCCTCGGCCTCCCAG | 51429 |
| rs539161387 | in-del | -/AAG | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157753555 | AAAACAGCCATGGTT[-/AAG]TCCAGAGAAGAACAA | 51429 |
| rs539180878 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157896208 | GTAGTTCCTTAGAAT[-/A]GACTAGCATCTCAGG | 51429 |
| rs539187468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157858978 | ACACAGCCAAACCAT[A/G]TCACATACTCTCCAT | 51429 |
| rs539187939 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157760255 | TCTTTCCACCTCTGC[G/T]TTCAGTGACTTCTTA | 51429 |
| rs539217557 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157936706 | TATGATTCTTAAGAT[G/T]TAATAGCTCATAAAT | 51429 |
| rs539218399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886036 | TAGTTACGATGGAGA[C/T]AGACAGACGTCGTGG | 51429 |
| rs539221809 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157828955 | GACTGTTTGTGATCA[C/T]TTTTGTATCTTCAAT | 51429 |
| rs539221861 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157855905 | CCACGCCAAGCTAAT[-/A]TTTTTTTGTTTTTTT | 51429 |
| rs539240481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157876417 | GATCGTGCCACTGTA[C/T]TCCAGCCTGGGCGAG | 51429 |
| rs539246912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157751021 | TGTTGGCAGGAATAC[A/G]AAATGGTGCAGCCAC | 51429 |
| rs539249983 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157786059 | CTTGTTTTTTTAAGA[C/G]ACAGACAGGGTCTCA | 51429 |
| rs539279325 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157879194 | GCAGAACGCAGGTTT[C/G]TGGGCAAGAACGTTT | 51429 |
| rs539285022 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157744121 | TATATAAAACAACTA[A/C]TCTAATGCCTATAAT | 51429 |
| rs539303175 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157716514 | ACGTTCTTCCTGTGG[C/T]ACTGGGAGGCGAGCC | 51429 |
| rs539303263 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157852371 | TCAAAAGCTGCTTTG[C/T]ATTAGGCCATGGTTC | 51429 |
| rs539326305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157756796 | CAGAGTCAAATATGC[A/G]GGAAAGAATCTGATT | 51429 |
| rs539340285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157792416 | AGTGCTGGGATTACA[A/G]GCATGAGCCACTGTG | 51429 |
| rs539365578 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157825532 | ACACGAGCCTTAAAG[C/G]ATGCGTAAGGACTTC | 51429 |
| rs539365677 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157930348 | GCCCTGAGAAAATAA[C/T]GTATACAAATGCAGC | 51429 |
| rs539366424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157845311 | AGACGGCGTTTCACC[A/G]TGTTGGCCATGCTGT | 51429 |
| rs539377071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157793094 | GGGATTACAGGCATG[C/T]GCCAGCACACCCAGT | 51429 |
| rs539383900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157905204 | AGAGAAAGGAGACTC[A/G]AGGGAAGTCAGCTGA | 51429 |
| rs539403862 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157792467 | TTAATTGACAAAAAT[A/G]TATATCTTTATCATG | 51429 |
| rs539409808 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | SNX9 | GRCh38.p7 | 6:157827583 | TAAATATATATTATA[G/T]TATAGTTTATATATA | 51429 |
| rs539410213 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157859724 | TGTCATGCATTTAAG[C/G]GCCATTGTATTCTTT | 51429 |
| rs539420090 | snp | C/T | 8.24029e-05 | 0.00641831 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157938737 | CAGCATCATGTCTTA[C/T]GCGTTGCAAGGTAAG | 51429 |
| rs539426130 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157811400 | AATTAGGGATCACCC[C/T]ACTCTGCCATCCAGA | 51429 |
| rs539475189 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, nc-transcript-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157892843 | TCACTTAGCTTCTGG[A/C]AGTCTTCTGAATCCA | 51429 |
| rs539478765 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157921008 | GGGTTACTCTTCATA[A/G]TGCTAAATTTAAACT | 51429 |
| rs539490585 | snp | C/T | 8.95071e-05 | 0.00668921 | intron-variant | SNX9 | GRCh38.p7 | 6:157906082 | GAGTTGTAAAATTCT[C/T]ACAAGGAAAGTCTTA | 51429 |
| rs539506813 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157768026 | TGGTTTGTCCAGGAC[C/T]ATCCCAGTTTTAAAA | 51429 |
| rs539508433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157773435 | TAGCAGGTGAGCCAG[A/G]CGACCTCGGCAGGAG | 51429 |
| rs539535516 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157806396 | GCACATTTGTGAAAC[A/G]TTATTCCATGGATAT | 51429 |
| rs539549504 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157852493 | GTGTATCTTAGGGCA[G/T]TTGAACTTCAAATAC | 51429 |
| rs539569531 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157744682 | TCACTGGAACCAACA[G/T]GGATGATGACAGCAT | 51429 |
| rs539573125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157738036 | TTTGTTATGGTTTGC[C/T]GAGGAGTGTTTTACT | 51429 |
| rs539587922 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157768622 | GGTACTTTTTTTAAC[A/G]TAAAATTTCCTGGGG | 51429 |
| rs539589066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157774134 | AGGCAGACGCAGCCC[A/G]GAGGGAGAGGACCCA | 51429 |
| rs539593311 | snp | C/T | 0.000233065 | 0.0107925 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157873161 | ACGAGGGCTGGTTCC[C/T]ACAGACTACGTTGAA | 51429 |
| rs539610818 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157933520 | ATAGTTCTCATTGCC[C/G]TGGCCTTACCATGTC | 51429 |
| rs539629845 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157825528 | TTAAACACGAGCCTT[A/G]AAGCATGCGTAAGGA | 51429 |
| rs539634036 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157758272 | AGGAAGGAAAAAGAA[A/T]AGAAAGAAAAAAGAA | 51429 |
| rs539642399 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886910 | CCTTTTGGAAGCCCA[A/T]TCAAGCTGAGTCTTC | 51429 |
| rs539648597 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157856041 | GGCGTGAGCCACCAC[A/G]CCCGGCCTGTCATTG | 51429 |
| rs539665808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157789271 | CCTAGTTCACCTTTT[A/G]TATAAATTTATATAT | 51429 |
| rs539674615 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157719311 | CCAGAAGCAAGAAAA[C/T]AGACATTGTCTCTAC | 51429 |
| rs539679116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894530 | GGTGGGATGGTGGGG[A/G]CAGGGCTAATAGGTG | 51429 |
| rs539714537 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157803361 | GTGTGAAGGGAAAGA[C/G]GGTTCTGTACCTAAG | 51429 |
| rs539714663 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157876862 | TGCCAGTCACATGCA[C/T]GCCACCTCAGTTGTG | 51429 |
| rs539718466 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885610 | GTTGCACGTGGTATA[G/T]TCGTAAGATGGGCCG | 51429 |
| rs539740283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157795664 | AACATAGATGAAACA[C/T]GGTGAAATATTAACA | 51429 |
| rs539748727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157899923 | CGTGTATATGTGCAA[A/G]TGCGTGCCTGTGGGT | 51429 |
| rs539748771 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157770563 | GAGGCCAAGGCGGGC[A/G]GATCACGAGGTCAGG | 51429 |
| rs539776023 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157853320 | GCAGTTATTCTTTGT[G/T]CCACTGTATGTAATA | 51429 |
| rs539779674 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157788242 | TTGTCAATAAGCTTT[A/C]AAGGGTCTGAAAAAC | 51429 |
| rs539781481 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157738554 | ATCAGATGGGTCTCC[G/T]GAATACAGCACAGTG | 51429 |
| rs539800895 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157826647 | CAAGTCTTGTTTTAC[A/G]AATATTAATACAAAA | 51429 |
| rs539822856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157732298 | GCTGCATTTACTACC[A/G]CATCCCAGCTGGCTT | 51429 |
| rs539844380 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157766316 | CTGGCGCTTCCCCTG[A/G]AATATAAAATGGAAC | 51429 |
| rs539846968 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157765730 | GGACCTGGCATAGAT[G/T]CAGCAGTGTCACCCT | 51429 |
| rs539851084 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157863662 | GGAAAATAGATGGCA[C/G]TTGGGGTTGAGGCCA | 51429 |
| rs539882741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157896135 | GATTCATGAATCTCA[A/G]GTAAAGGCCAAGTCG | 51429 |
| rs539892881 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157815262 | CTGTTGCCCAGACTG[C/G]AGTGCAGTGGCCTGA | 51429 |
| rs539893258 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157926695 | CTGAGGTGGGAAGAT[A/T]GCTTGAACCTGGAAG | 51429 |
| rs539894602 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157770698 | CCCAGCTACTTGGGA[A/G]GCTGAGGCAGGAGAA | 51429 |
| rs539895568 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157918909 | TATTTTTATATATAT[A/T]ACATCTGTATGTTAT | 51429 |
| rs539896409 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157776412 | TTATGGAAAAAAAAT[C/T]CTGGGGGAAGATTCT | 51429 |
| rs539899678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157790048 | CACCGTCGCCAGGAA[A/G]GAGGAAGGCAGGGAG | 51429 |
| rs539906341 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157880103 | TCTGTTTCACACCCC[G/T]CCAGTCCCCAGGTGA | 51429 |
| rs539957181 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157919321 | TTGTCTCACTCTCTC[G/T]TCTTCCTCTGGGATT | 51429 |
| rs539961339 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157825969 | TATAAGTATTAACTG[A/T]TGAAAAGTAAATTCA | 51429 |
| rs539964645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157782076 | CAAGATGGGTCCGCA[C/T]GTAGACCTTACTAAA | 51429 |
| rs539995415 | in-del | -/TTG | 0.488965 | 0.0734569 | intron-variant | SNX9 | GRCh38.p7 | 6:157759850 | CCATCAAAGTTTGTT[-/TTG]TTTTTTGTTTGTTTG | 51429 |
| rs539997390 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157812889 | ATAGGAAATACACCA[A/T]TAGAATGGAATCTGG | 51429 |
| rs540009103 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157800059 | TCACAGTTTTCACAT[A/T]TGCTGAATTTTCCAG | 51429 |
| rs540014064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157717294 | CCTGGTCTAGAACTC[C/T]TGGGCCTCAGACTCC | 51429 |
| rs540017854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157853993 | ATTTGAACCTATGTG[C/T]CTGGCTTCAAAGCCA | 51429 |
| rs540038480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157940333 | CATTTGGGTGATTTA[C/T]CTGTATTGGATTTTA | 51429 |
| rs540039278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157929324 | ATAGAAAAATAGTCC[C/T]GTATCCAGCTGTAGG | 51429 |
| rs540041578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157724902 | ATTTTATATCAGGGA[C/T]GTGAGTATCCAAGGA | 51429 |
| rs540044196 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894255 | GCTGGGATTACAGGC[A/G]CCCACCACTACACCT | 51429 |
| rs540048642 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157898710 | TAAGAAGGTAGTCTC[C/T]CATTATTTTTTAACA | 51429 |
| rs540051925 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157758722 | AGCCCCATGAGGGTG[A/G]GACTGTGGCTGAGTC | 51429 |
| rs540058052 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157881648 | CACTTGAATGATAAG[A/G]AAGTGAAATAGCCTT | 51429 |
| rs540077836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157717871 | GAATATATTGCACAG[C/T]GGTGAAATCGGGGCT | 51429 |
| rs540080720 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157803856 | GAAACTAATTCTGAC[-/T]TTTTTTTTTTTTTTT | 51429 |
| rs540089713 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890412 | CAATGTCAAGCCTGC[A/T]TAAATATATTTCTCT | 51429 |
| rs540103859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157725319 | TGTGGAGCTACTTAG[A/G]TCTGTGGGTTGGTTA | 51429 |
| rs540111981 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157944889 | AAATAAGAGAATCCA[C/T]GGGATTTGATGCCTG | 51429 |
| rs540113353 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157765911 | CTTGGGTCCATGAGC[A/G]TTGTTGTCTGGGAGC | 51429 |
| rs540119833 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157820062 | TCTAAAGGCAGGCCT[G/T]CGTAGAGAATCAACT | 51429 |
| rs540130364 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157906708 | GAGTTAAAGACATCA[C/T]TGAGAATATCTGTCT | 51429 |
| rs540139625 | snp | A/T | 1.65091e-05 | 0.00287303 | intron-variant | SNX9 | GRCh38.p7 | 6:157896790 | CATGGTTTCCAAAAG[A/T]CACAAAAATTCTCCT | 51429 |
| rs540162391 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157769522 | CTGAAGGCTGAGTAA[C/G]CGTCAGCCAGGGGAA | 51429 |
| rs540189043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157814449 | AGAAAGCTCAGATTA[C/T]ACTTCTTTTGAAATT | 51429 |
| rs540195978 | in-del | -/AA/AAA | 0.325799 | 0.238232 | intron-variant | SNX9 | GRCh38.p7 | 6:157902212 | CTGAGAAGCTTACTT[-/AA/AAA]AAAAAAAAAAAAGGA | 51429 |
| rs540201365 | snp | A/C/G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157789757 | AATCACAGAATAAGC[A/C/G/T]CTCAGTCTCAGTTAT | 51429 |
| rs540204907 | snp | C/T | | | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157944098 | AGGACCTTGGCACAC[C/T]GTCAGCTCGAACTCA | 51429 |
| rs540227146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157829793 | CCAGATATATAAAAG[C/T]CAATAGCTGAATTTT | 51429 |
| rs540231905 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157731586 | CTGAATGAGTTAACA[A/C]CTTGTGAAGTCTTCA | 51429 |
| rs540264110 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822773 | GGGGCAAAGACAGCG[A/G]GGTTGCGGGGCTCCT | 51429 |
| rs540267389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157741219 | CAGGTGTGGTGGCAC[A/G]CACCTGTAATCCCAG | 51429 |
| rs540272713 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157922452 | ATAAATTATGAAGCT[A/C]TTTTTGTCTTTAATG | 51429 |
| rs540284465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157777831 | AGCTAAGTGGTGCTC[C/T]GTATGCAGCTGCTCT | 51429 |
| rs540307675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157868768 | TTTCATTGCAGGCTT[A/G]TATAGATGGAGAAGG | 51429 |
| rs540315905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157936765 | AGGGTAGGTCCTTGT[C/T]ATAGCTACATAGCTT | 51429 |
| rs540334501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157809473 | CATAAACTGTAAAAG[A/G]AAAAAATGATAAGTT | 51429 |
| rs540335042 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157729103 | AGCAAGACTCCATCA[-/A]AAAAAAAAAAAAAAT | 51429 |
| rs540337198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157829108 | TTAAAAGTGTATACA[A/G]GTACAACACAAAATT | 51429 |
| rs540357378 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157726844 | ACAACACAGGAGTTT[A/T]AAAAAATTCAGAACT | 51429 |
| rs540372850 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157863133 | CCCAACTCCCATACC[A/G]AAGAGCTCTGAGAAA | 51429 |
| rs540395569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889983 | GTGTGGGGACTAAGA[A/G]AGCTAAGTAAATTAC | 51429 |
| rs540404634 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157795553 | ATTATGATTATATAA[-/G]AAAATATCCTTAGGT | 51429 |
| rs540410397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157729724 | TTCGGGAGGCTGAGG[C/T]GGATGGATCACCTGA | 51429 |
| rs540414674 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157754498 | TACTGGAAGGAAGCA[A/G]TTGGGTGGCTGCATT | 51429 |
| rs540417260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157729750 | CCTGAGTTCAGTTCG[A/G]GACCAGCCAAAACAA | 51429 |
| rs540447524 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157872484 | TGAGCTGCACTGCGT[A/G]TGTCTGCAATCACTG | 51429 |
| rs540479857 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157857997 | TAGTCTTAGGTGGCC[G/T]TTCCTTCATGTTAGG | 51429 |
| rs540480977 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157916362 | TAATGTAGACAATCA[C/T]GTCAGCTTGGAATAG | 51429 |
| rs540482176 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157772770 | GTGTGAGGTTAAGAA[A/G]ACTAGGTTAAGGCAC | 51429 |
| rs540501025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157856120 | TTGGGTGAAGAGACA[C/T]TTCTCCCATTCTCCC | 51429 |
| rs540501651 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840768 | TGGGAGAAAAAACTT[C/T]GTAAAGAAATTTTTA | 51429 |
| rs540535722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157753857 | GCTGTATGGGAGACT[A/G]GAGTTTTATTATTAC | 51429 |
| rs540544352 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | SNX9 | GRCh38.p7 | 6:157823504 | GGGGCGGCGCGGAGA[G/T]GGTCGGGGCCGGGGC | 51429 |
| rs540564324 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157848710 | TACTGTGCTGAGCAG[G/T]ACTGACAGGGAGCTT | 51429 |
| rs540571924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157734709 | TCTTGAACAAAGGCC[C/T]CTCCAGCGTTATGGG | 51429 |
| rs540581575 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157833622 | TTGCTGTTTCATAAA[C/T]ACATTGGTAATTTTA | 51429 |
| rs540589669 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157910177 | GCTATGAAGAGAGAA[C/G]CATTGCATGTTGTAC | 51429 |
| rs540594504 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157876666 | TACTTGAGAACATTG[G/T]CCAGGTAAGGGTTAC | 51429 |
| rs540655013 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157815097 | TAACCACAGGTTCTC[C/T]AAAACACAGGTGTTT | 51429 |
| rs540655189 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157869919 | CACCTCGCACCCTCA[C/T]ACACCTCTCATGCTC | 51429 |
| rs540662025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157826145 | CTACTATATTTTACA[A/G]TAAAAAAGGAAATTA | 51429 |
| rs540667152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157737632 | TGATTTTTTGAAGAG[C/T]TTTTCGTGTCTCTAT | 51429 |
| rs540692973 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157836257 | GATAAGTGGAAACAT[C/G]TTGTGCACGTTCTGG | 51429 |
| rs540702594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157755046 | CACTTGTAAACTGTC[A/G]TGGTGCAGGTGGGAG | 51429 |
| rs540713519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157785534 | AAAGGATAAAAACCA[C/T]ATGATCATTTCACAG | 51429 |
| rs540735830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157832053 | CATTTTTCTTTTGAC[C/T]ATTAAAAGCACATGA | 51429 |
| rs540737230 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157900025 | AGTCCTCATGCTGTA[C/T]ATGAGATCTCTAGAC | 51429 |
| rs540763922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157788805 | GGATTGGAATCAGAA[A/G]TCCTGGGTTCAAATT | 51429 |
| rs540780302 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SNX9 | GRCh38.p7 | 6:157743500 | CAAAACAACAACAGA[C/T]AAACAGAAAACTCCA | 51429 |
| rs540798266 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157760661 | GGATATGGGGACTGG[C/G]AGGAAGTAGTTTCCG | 51429 |
| rs540818053 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157725038 | CAAAGTTTAGCATTC[A/G]TTTCTGAAAGATGTT | 51429 |
| rs540818080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157732497 | ATTTACATTGTGAAA[C/T]GATGGCTACAGTCAA | 51429 |
| rs540840403 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157945187 | AGGAGCAGCAGTCCC[A/G]GGATGTCAACCCACT | 51429 |
| rs540871228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157898062 | AGATACACCTTGCAC[A/G]CCTAACATTCAGGAA | 51429 |
| rs540889027 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157763511 | TTCCGTGGTTGACCC[A/G]GAAGCAAGTCAGGCA | 51429 |
| rs540904466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157864535 | TTTGGAAACTAATTG[A/G]ATTCAGCTGGATTTT | 51429 |
| rs540914340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157870295 | TCACATATGCACTCA[C/T]GTGTGAGCACGCACA | 51429 |
| rs540919608 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157912637 | TAAGAATTCCCCTCT[C/T]GCTCAACTACTGGAG | 51429 |
| rs540945412 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157815933 | CCTAATGTAGGTGAC[A/G]GGTTGATGGATGCGG | 51429 |
| rs540955017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157731842 | CAACTAGGTTTCCTA[C/T]TGGAGATCTCAGTCT | 51429 |
| rs540959903 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157793805 | TATTTTCTTGTGTGG[C/T]TTATAACCTGATTTG | 51429 |
| rs540965853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157857417 | ATGAAAAATGCTGCT[C/T]GGAATTCCCAATCTG | 51429 |
| rs540967772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157772589 | TGGGGAGAGCATGGC[C/T]ACAACGCCGCCTTGG | 51429 |
| rs540969788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157766929 | GGTTGTTTTGAAAAT[C/T]AGAAATATATATAGG | 51429 |
| rs540973700 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157863575 | AAATAGTTGAAGAAT[-/G]AGTTCTTGAAGTATA | 51429 |
| rs540979604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157879515 | TTTTCTTATTCAAAT[A/G]CAGATTTTATATTAC | 51429 |
| rs540990250 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157754848 | GAGTCCATAGAATAA[A/G]GTGAAAGCAAGTGTA | 51429 |
| rs540990457 | in-del | -/TAAA | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157817874 | GGGAGACTCTGACTC[-/TAAA]TAAATAAATAAATAA | 51429 |
| rs540999464 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157769791 | AGCACTGGGTGTGTT[G/T]TGGGGAGGGATCTAG | 51429 |
| rs541011904 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157752358 | CATATGGAGGATCTG[C/T]GCAGGCACCAGTCTC | 51429 |
| rs541012419 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157856617 | GCATATTACTATCAC[A/G]ATCAATCTTCTCTTC | 51429 |
| rs541019087 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157801565 | GAAACCCTGTCTCTA[C/T]AAAAAATACAAAAAT | 51429 |
| rs541027588 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157781352 | TTAGGACATTTGCTC[C/T]GTTGGGGCATGTACT | 51429 |
| rs541039905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887689 | TATTTTTTGTTTTCA[C/T]TGGGAGCATAAACTG | 51429 |
| rs541050178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157840359 | TTGGCAATAAAACCA[C/T]TGGAGGGTTTTCACC | 51429 |
| rs541054186 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157759013 | AGTGGAAGAAGACCT[C/G]AGGTCCTGAAAAACA | 51429 |
| rs541094572 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157817311 | GATGCCTGATGCCAC[A/G]ACCAAGGCCATCTCT | 51429 |
| rs541126743 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157878985 | TTTTAAGATTCTTCT[A/T]TCAAACTAGCAGAGA | 51429 |
| rs541131402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157839670 | ATAATATTTTAGTTC[C/T]CAGGCCACCGCCTCT | 51429 |
| rs541133737 | snp | A/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887924 | TGGAAGCTGGGCTCC[A/G]GAATGGTCCTCTTAA | 51429 |
| rs541140136 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SNX9 | GRCh38.p7 | 6:157765346 | TTTGAAATATATTTG[G/T]TTTTTTTTGTTTGTT | 51429 |
| rs541142131 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157940091 | GCTGGTGCTCAGGGG[A/C]AGCAAGGCTTCCCGT | 51429 |
| rs541145943 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157774646 | TGGGAGGAGCGCCGG[A/G]TCACATTTCCTCTTG | 51429 |
| rs541182861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157845617 | GTGGGGTCAGAATTT[C/T]CTGTGTATACTAGAG | 51429 |
| rs541187861 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157882107 | TTAAGGGGCTAATGC[A/G]GCTGGTAACTTTATG | 51429 |
| rs541187964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157874410 | TAAGTTGATATTGGC[A/G]GTAATTGGATTTTCT | 51429 |
| rs541192308 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157819316 | AGAGAGCAGGGACTT[C/T]TGTCTCCCTCACCTG | 51429 |
| rs541204801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157906265 | AAGCTCTTTCTTATA[C/T]CGTACTTTAAAGCTA | 51429 |
| rs541206437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157934014 | TCCCATTACAAAGGA[C/T]AGTGAAGGTCAGCAG | 51429 |
| rs541232858 | in-del | -/TCT | 0.00953873 | 0.0683987 | intron-variant | SNX9 | GRCh38.p7 | 6:157879494 | AACTGAATCAAACTC[-/TCT]TCATTTTCTTATTCA | 51429 |
| rs541244255 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157775731 | CCTTCTGTTTTCATA[A/C]ATTTGCCACCAGCAC | 51429 |
| rs541249231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157874914 | TAAAATATGAGTATG[C/T]GGCAAAAGCAGTGCT | 51429 |
| rs541251001 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157716596 | CAAGGAGGGAGGGAT[A/G]CTTTTAGCATGAGCG | 51429 |
| rs541260542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157835261 | CAAGTGATCCACCTG[C/T]CTCGGCCCCTCAAAG | 51429 |
| rs541266191 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157899960 | GTGGTAAGAGCACCT[A/G]AAATCTCCCTCAGCA | 51429 |
| rs541271122 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157919697 | TTGTTTTTTTCTGCC[A/C]AATTCAACATCTGCG | 51429 |
| rs541282978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157784452 | TCACTGCAAACTCTG[C/T]CTCCCAGGCTCAAGC | 51429 |
| rs541286726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157868021 | CCTAGCATGATAATA[C/T]TGTATCTCTAGAATA | 51429 |
| rs541297387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157739969 | TGGGAGCCTAGGGGA[A/G]GGATAGCATTAGGAG | 51429 |
| rs541318750 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157869750 | ACACCCCACCATGGG[A/C]CCCATCAGACCTCGC | 51429 |
| rs541323218 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157881308 | GCGAGCTTAATTGAC[A/G]TGTTTTATGTGTTCC | 51429 |
| rs541328253 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157774481 | AGGGTGAGGGGCAGA[C/G]CACAGATGGGGCGAT | 51429 |
| rs541335584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157745747 | CGAGAATATGAAAGA[C/T]TTACTTATAAAAGGG | 51429 |
| rs541347704 | in-del | -/TGTT | 0.214166 | 0.247418 | intron-variant | SNX9 | GRCh38.p7 | 6:157919957 | TCAGTTATTGCTGTT[-/TGTT]TGTTTGTTTGTTTGT | 51429 |
| rs541352617 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157905892 | AGCAAATAGAGTGCC[C/T]GTAAACATCACACCT | 51429 |
| rs541357863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157867359 | GAACAGGGCTATCAC[C/T]GTTGGTGTTATTCTT | 51429 |
| rs541369164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157774791 | TGCTCCACCCTCCCC[A/G]ATGGCCTGGGGAGAG | 51429 |
| rs541390432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894755 | AATGTGGGAATGTTA[C/T]TGCATTCTCTTTCAA | 51429 |
| rs541406675 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157761095 | GGGAGTCAGGGTGCA[C/T]TGTCTGCAGAGAATT | 51429 |
| rs541408091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157798120 | ACTAGCATCAAAAGA[A/G]AAAAGGGGAGAAAAC | 51429 |
| rs541419108 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157934930 | GGTTCCTATCAAAAG[A/G]CTTAGATACCAATTG | 51429 |
| rs541427311 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157779952 | TGTTCTAGTCTATTT[C/T]GTTTACTAACAATGG | 51429 |
| rs541434759 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157744896 | ACTACAGGTGTGTGC[C/T]ACCACACCCGGCTAG | 51429 |
| rs541442918 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157798502 | AATTGGTGACATTTG[A/C]ACATGGTCTGATGAC | 51429 |
| rs541450670 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157850282 | GCAAGGCTTGACTAG[C/T]GCAGGGTGAAGAGTG | 51429 |
| rs541452131 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888361 | CATTAATACTGTATC[A/T]TGATGCCAAACAACA | 51429 |
| rs541464700 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157937273 | TCAAAGTATGGCAGT[C/G]TTGGGAGTTATTTTC | 51429 |
| rs541474319 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157763963 | CAAAGCAGGTGTCAA[A/C/G]GTTCATTAATCTCAT | 51429 |
| rs541488302 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157857247 | TGGTACCTGTGTCTT[G/T]TTGACACAACCAGTA | 51429 |
| rs541512979 | in-del | -/TGTT | 0.0175622 | 0.0920472 | intron-variant | SNX9 | GRCh38.p7 | 6:157919954 | AAGTTCAGTTATTGC[-/TGTT]TGTTTGTTTGTTTGT | 51429 |
| rs541522072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157766784 | CTGTACCCCCAATAA[A/G]TCTTTGTTTCCTCAA | 51429 |
| rs541527435 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157743027 | TTAATTTAAGATTAA[C/T]AGTCATTGCTTGGAG | 51429 |
| rs541538831 | snp | G/T | 0.0352966 | 0.128072 | intron-variant | SNX9 | GRCh38.p7 | 6:157900477 | AGGCGGATCGGCCCG[G/T]TGAGAAATAATAGAC | 51429 |
| rs541550203 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157857958 | CGTGGTTCTTGTGGT[C/T]TGGAGAGCCCATCTG | 51429 |
| rs541568583 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157760490 | GCCAGAGTGGCCTCT[A/G]TCTCAATCAGTCTGG | 51429 |
| rs541573617 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157748295 | AAAAAAGAATTTAGG[A/T]CAACATTGGATATCT | 51429 |
| rs541622169 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157770895 | GCACTGAAAATAAAA[-/T]TATTGTTGTAAAGGT | 51429 |
| rs541627686 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157733104 | CCAGCGTTTCCCAAG[G/T]TTCCGACTGTCCTAG | 51429 |
| rs541666207 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157925709 | CCAGGCACCAAAGAA[C/T]GCATTTATAGGGCTC | 51429 |
| rs541672162 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157896720 | ATACATTTCTATTAA[C/T]TGTTTTTAGTACTCC | 51429 |
| rs541681927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157840870 | GAAAGTGAATACAAA[C/T]GGCTCATCAGACCAT | 51429 |
| rs541692643 | in-del | -/C | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157755933 | AGACCACACAGTGTT[-/C]CTTTGAAACTCCTGG | 51429 |
| rs541697689 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157829724 | AATGCATTTTTTCTT[A/G]AAGACTATATTTCTA | 51429 |
| rs541699954 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157805262 | CCAGCAGTCACCAAT[C/T]GCTCCATCTCCCGTG | 51429 |
| rs541705225 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893226 | GCCTTCATTTCCAGC[A/G]TCCACTGGGGTCATC | 51429 |
| rs541708940 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157927904 | ATAAAATTATTGCGT[A/T]TGTGTTACCAAAAGT | 51429 |
| rs541722819 | in-del | -/AA | 0.373598 | 0.21731 | intron-variant | SNX9 | GRCh38.p7 | 6:157735961 | GTGAGACTATGTCTC[-/AA]AAAAAAAAAAAAAAA | 51429 |
| rs541740029 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157794270 | ACCATGTAAGACATG[A/C]CTTTGCTCCTTCTTC | 51429 |
| rs541761275 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157806743 | CTGAAAACTGGGACA[A/G]CTGCATTTTTGGACC | 51429 |
| rs541766875 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157748521 | GGGTCACAAGGTCAG[A/C]AGTTTGAGACCAGCC | 51429 |
| rs541800286 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157842843 | CTCTTGGAGCCAGAG[A/G]CTACATGACCCCGAA | 51429 |
| rs541801103 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157801006 | ATTATTTTGACACTA[A/C]ACTTGGAGGTGAGCT | 51429 |
| rs541824549 | in-del | -/A | 0.162581 | 0.234218 | intron-variant | SNX9 | GRCh38.p7 | 6:157865341 | CGAAACAGTCTCAGG[-/A]AAAAAAAAAAAAAAA | 51429 |
| rs541839805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157866154 | TCTCTCTTGGGATAC[A/G]TGCACAGCAGTGTTC | 51429 |
| rs541862578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157723275 | ACCTCTATTTTCACT[A/G]ACCTACTTTCTACAC | 51429 |
| rs541867310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157810041 | TTATTCACTATAACC[C/T]TTAACTGGAAACAGC | 51429 |
| rs541876638 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157838423 | CTAATGGAGAACACA[G/T]ACACTTAGATATCTT | 51429 |
| rs541888764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157801626 | CCCAGCTACTCAGGG[A/G]GCTGAGGTGGGAGGA | 51429 |
| rs541896694 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157875537 | CAGTGTCAGAGCCTC[A/G]GCCTGGATCAGGAAA | 51429 |
| rs541916502 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157779556 | GTCTACGCAGACAAC[C/T]GTATGTGTTCGAGTC | 51429 |
| rs541934519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157870874 | CACAGATGCAGCACT[C/T]ACCCGTGCAAGCACG | 51429 |
| rs541935010 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157877789 | TTCAGCTTGGCACAC[G/T]CTGCCAACTTCTGAG | 51429 |
| rs541935452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157849532 | TGAATTGGAGCAAGG[C/T]GCAGCAGGTGTGCAG | 51429 |
| rs541960160 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157786086 | CTCAGTCTGTCAGCC[A/T]GGCTGGAGTGCGGTG | 51429 |
| rs541962617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157807880 | TTCCCAGTGAAATAC[C/T]GAAGTTCCAAACCTG | 51429 |
| rs541988840 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157936757 | CCCAGGACAGGGTAG[G/T]TCCTTGTCATAGCTA | 51429 |
| rs541990134 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157802873 | GATGAACTTGCAACA[C/T]CCCTGGACATTAGAG | 51429 |
| rs541996765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157916584 | TAGATGTGCTTTTAT[C/T]AAGTTAAGGAATTTC | 51429 |
| rs542001622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157865716 | TTTTTATGTATTTCA[A/G]GATAGCATTTTGGCT | 51429 |
| rs542005977 | snp | C/G | | | utr-variant-5-prime | SNX9 | GRCh38.p7 | 6:157766390 | TGCTCCCCAGACCAT[C/G]TTCCGTGCTCCCCAC | 51429 |
| rs542012950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157787664 | TTAATATCATCATTA[C/T]GAATTCTGAGAATAT | 51429 |
| rs542026398 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157836639 | ACTCTCGCCCAGGCT[A/G]GAGTGCAGTGGCGCG | 51429 |
| rs542062647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157736206 | GAAAGTCAATGGTAG[C/T]ATGATGGGGATAGCA | 51429 |
| rs542065294 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | SNX9 | GRCh38.p7 | 6:157795826 | AATTTAACCTAAGTA[A/C]AATTTCAATGTTGGA | 51429 |
| rs542074482 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157858164 | TAAGTGCTTTTCATG[C/T]CTATGTTAGTATCAC | 51429 |
| rs542078414 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157747833 | AATATTATTAATAAT[A/T]CCAAATGTTTATTGA | 51429 |
| rs542083038 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157830943 | TACCTTCTGTTCACT[A/G]TTCTTTCCTCAGTCA | 51429 |
| rs542087804 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157747355 | ACTCTCTTAGCCATG[A/C]TTGACCAAATCATCT | 51429 |
| rs542093821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885805 | TAACTGGTGGACTTA[C/T]CAGATGGGATGATCT | 51429 |
| rs542102262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157802360 | CTTCCTAATGAGGTG[A/G]CAATGGGGCAACTTG | 51429 |
| rs542113804 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157930789 | GAAAGGTTGGGGACC[A/G]TTGCTCTAAAGTATA | 51429 |
| rs542137753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157924221 | TAAATATATATATGT[A/G]TGTATTATATTTCAA | 51429 |
| rs542173187 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157931630 | CTTCCCTGGTCATGC[A/G]AAGTCTGACTGTTGT | 51429 |
| rs542184566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157911532 | TCCTGGACACTTCCC[A/G]AGTGCCTCTCATCTG | 51429 |
| rs542213311 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157866303 | AAAATTTCATTTAGG[G/T]CTGGTCATAGTGGCT | 51429 |
| rs542222642 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157943318 | TTTATAACTCCTTTC[A/T]GTCCTCTGGGGCTCC | 51429 |
| rs542229626 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157743729 | CTATTTTAATCATAA[A/G]TAAGGCCAGGCATGG | 51429 |
| rs542265029 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157907838 | ACTCATGAAACAGAG[C/T]CCCGTGAAATTGGGC | 51429 |
| rs542266151 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157771134 | AATGACTAAGAATAA[C/G]TTAGTCATTTATGAC | 51429 |
| rs542268505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157722811 | AATTCAAGACCAGCC[C/T]GACCAATATGGTGAA | 51429 |
| rs542306866 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157928205 | GGTGATTGTGTATCC[A/T]GGTTATTGTCTCCGT | 51429 |
| rs542323003 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157827565 | TATAGTTTATATAAT[A/G]TATAAATATATATTA | 51429 |
| rs542356029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157774883 | AATTCCCCCTAGTCC[C/T]GTGAATGCAAGGCCA | 51429 |
| rs542390980 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157741732 | CATCAGCATTCTCCT[C/T]GCACAAATTCACCAA | 51429 |
| rs542395762 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157730022 | AATGGGTGTGGGGGC[A/G]GGGAGTTGGGGCTGA | 51429 |
| rs542398301 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157770288 | TCCATCAGAGCAGTG[A/C]ACGCATGGAAGACTT | 51429 |
| rs542412793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157939289 | GGAACAAAAGCCACA[A/G]AATTGTGGTGCTAGA | 51429 |
| rs542420140 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157935516 | AACACCCCACGAAAA[A/G]AAAGGTGCAGGGAAA | 51429 |
| rs542439724 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157719036 | TCCCCAGCCACAACT[A/C]CCTGATGAGGCAGTG | 51429 |
| rs542467642 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157768834 | CACCTGAGGTCAAGA[C/G]TTTGAGACCAGCCTG | 51429 |
| rs542476456 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157837028 | GTTGGTCCCTAAGAT[-/C]TGTGAGGCCGTAAAT | 51429 |
| rs542500671 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157857148 | CATGAGTTTAAGCAA[A/C]TTTAATGTTTCAGTC | 51429 |
| rs542507513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157851487 | GTATTGCATTAAACA[A/G]TAACTCCCCATTTCC | 51429 |
| rs542512866 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157833996 | CACGCTGGGGGCTAC[A/G]TCAGGTTTTGTACTT | 51429 |
| rs542525829 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157727459 | ACCTTCAAGGCCTGT[C/G]TCCTAAATTCTATTT | 51429 |
| rs542530627 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157814322 | ACAACTTCTGTGCCA[G/T]TAAACATGGTCTAGC | 51429 |
| rs542538171 | in-del | -/TC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840472 | TCCTTCCTTCTCCCT[-/TC]TCTCTCTCTCTCTCT | 51429 |
| rs542567115 | in-del | -/CCGAGATTAAAAACAGCCATGGT | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157753531 | GGTGGTTGCCAAATC[-/CCGAGATTAAAAACAGCCATGGT]TAAGTCCAGAGAAGA | 51429 |
| rs542579685 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157769550 | GAAGACAGAGAGGAA[A/G]GGCGATTCAGGCAGA | 51429 |
| rs542580623 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157817300 | TTCAAGCCAAGGATG[C/T]CTGATGCCACGACCA | 51429 |
| rs542581187 | in-del | -/GCCCACC | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157897652 | GCTGGAATTACAGGA[-/GCCCACC]GCCCACCGCCCACCG | 51429 |
| rs542603794 | snp | G/T | 0.0244538 | 0.107838 | intron-variant | SNX9 | GRCh38.p7 | 6:157765355 | TATTTGTTTTTTTTT[G/T]TTTGTTTGTTTGTTT | 51429 |
| rs542639286 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157733059 | ATGGCAGGCACAGCT[C/G]CAGCCTTCTGTGGCC | 51429 |
| rs542681680 | snp | A/G | | | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157944066 | CCAGCGCTTCACTTA[A/G]CGGCATAAAGCAAAA | 51429 |
| rs542687128 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157874302 | GGCCCCTGGCCTCAC[C/T]CCGTAGGTCTTATGT | 51429 |
| rs542692131 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157904764 | TTGCAGGTTAGCCTA[A/C]TTCATTAAGCATTCA | 51429 |
| rs542709620 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157827973 | AAAAATAATGGTAGG[C/G]AATAAATGAATTACT | 51429 |
| rs542725240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157835460 | CTCTGTTGCCCAGGC[C/T]GGAGTCCAGTGGTGC | 51429 |
| rs542759262 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157841563 | CTGCACAGCCCATGT[A/G]GGGTGTGGGGATCGG | 51429 |
| rs542784506 | in-del | -/GT | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821443 | CTTTTCCACATACTA[-/GT]GTGTGTGCTCTTAGC | 51429 |
| rs542795483 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157848046 | AGCCCTTACTCTGTC[G/T]CATCACCTGATTAAC | 51429 |
| rs542807074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157735136 | AAATGAGCCAGGCAT[A/G]GTGGTGCACACCTCT | 51429 |
| rs542819598 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157728965 | AATTAGCCAGGCATG[G/T]TGGTGGCAGGTGCCT | 51429 |
| rs542827051 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157759869 | TTTGTTTGTTTGTTT[G/T]TTTTTTGTTTTCTTT | 51429 |
| rs542838621 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157933210 | GAAGCAGAAGGATCG[C/T]TTGAGCCCAGGAGGT | 51429 |
| rs542842954 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822645 | CGGCCTGAGGGAGCC[G/T]CCGGGCAGGAGGAAG | 51429 |
| rs542870137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889182 | ACGCCTGTAATCCCA[A/G]CACTTTGGGAGGCGG | 51429 |
| rs542894936 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157796112 | CAGGATGCCTTTAAC[C/T]CATGGATTTAAGTGA | 51429 |
| rs542908760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157854542 | ACTAGTTGTGTACAT[A/G]CAAACACGTATGGCA | 51429 |
| rs542915498 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157829647 | CTACATTTACAATTA[A/G]TATTATTTTCTAGGT | 51429 |
| rs542918058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157901228 | ATTTACAATAATCAG[A/G]AGCATTTCATCTTTT | 51429 |
| rs542950849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157941286 | TCTGTGCACCAGGAA[C/T]GGTGCTGAATGAGAT | 51429 |
| rs542956542 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157799238 | CCTCCCCTGACACAC[A/G]GGGATTACAATTCGA | 51429 |
| rs542991001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157838979 | TTGATTTCCAGGTAA[A/G]CTGTTGTTTGATGTG | 51429 |
| rs542999753 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157922207 | CATCTGTTCTTCATT[A/G]AAATCAAGGAAACGT | 51429 |
| rs543002086 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157740129 | AAATCTTTATTTAAC[C/T]AATGTTCACAAGTAA | 51429 |
| rs543013286 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157784643 | GTGCTGGGATTACAT[A/G]CATGAGCCACCAAGC | 51429 |
| rs543022110 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157875922 | AAGGCAGGTGGATTG[C/G]TTGAGTGCTGGAGTT | 51429 |
| rs543044399 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157743313 | GGTGACAGTACCATC[A/T]AATGGGCCAGACATC | 51429 |
| rs543045415 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157925506 | AGAAATGCAGGCACA[A/C]AGACACCAGGAGACA | 51429 |
| rs543079319 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157769774 | GAGGCAGTGGAAGGG[A/G]AAGCACTGGGTGTGT | 51429 |
| rs543087463 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157791989 | AAAAGCAAAACTCCT[C/T]CATATTGTTGCTTGT | 51429 |
| rs543119188 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157756345 | TTGAACCCAGGAGGT[A/G]GAGGTTGCAGTGAGC | 51429 |
| rs543134133 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157868737 | ATGTAACAAAAATTG[-/T]TATCAATTAATAGTA | 51429 |
| rs543135022 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889905 | CATACTGTGGGCTAG[A/C]TGCTTTGTATGCATT | 51429 |
| rs543151679 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157754376 | TGCAGTCGGTTAAGT[G/T]AGATCTCTCTCACTG | 51429 |
| rs543152006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157838224 | TGCCATGTTGCCCAG[A/G]CTGGTCTTGAACTCC | 51429 |
| rs543159533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157749610 | TGCAACCTCTGCCAC[C/T]TGGGTTCAAGCAATT | 51429 |
| rs543209548 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157720030 | ACTCCAGCCTAGACA[A/G]CAGAGTCAGACTCTG | 51429 |
| rs543215794 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157866960 | TTTGTTTGTTTGTTT[G/T]TTTAAGAGACTGCAG | 51429 |
| rs543258432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157915513 | ATTTCAGGCCAGGCG[C/T]GGTGGCTCATGCCTG | 51429 |
| rs543279313 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157931137 | TCCTCCTGTTTCTCA[A/G]AGTAGTTCTTTAAAA | 51429 |
| rs543287275 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157819077 | AAATGAAAACCAACC[A/G]ATCAGCTAACCAACT | 51429 |
| rs543313167 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157918261 | TAATTCTGTCACTTT[A/G]TTTTATGTATTTTGA | 51429 |
| rs543315522 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157832968 | CAAGTCCAGACTTTG[C/G]CTTGTCAGATCCCAG | 51429 |
| rs543328227 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821981 | CTCAAATGTTTCTTA[A/T]AAGGATTAAATGAGA | 51429 |
| rs543331421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157871758 | TAGCAGAGATTAAAG[A/G]TTCTTCAGTCTTACC | 51429 |
| rs543336737 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157772946 | AAGGCCACCCAGGGA[C/G]AATGGTGGGGAGAGA | 51429 |
| rs543338376 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157771941 | TGACCTCAAGTGATC[C/T]GCCTGCTTTGGCCTC | 51429 |
| rs543339097 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157777190 | AGGTCAGGAGATCAA[A/G]ACCACGGTGAAACCC | 51429 |
| rs543349601 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157845850 | AAAGAATTGATAGTA[C/G]ATGCTGAATTTGGTA | 51429 |
| rs543357131 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157908705 | GCAGACCTATTGTCA[C/T]CTAGCAGTGCCTAGA | 51429 |
| rs543371636 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157795737 | TATTCCCTCTGCTTT[C/T]ACACATAAACTTGTT | 51429 |
| rs543377577 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157777745 | AGGTTGAGCCTAAAG[C/G]ACTTGAAAGGCACTG | 51429 |
| rs543395943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885712 | TATGTGGTGATAGGC[A/G]GACCCCTGAATGCCT | 51429 |
| rs543396435 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157750554 | AAAAGTTTTGTGGCA[C/T]GGTCTTGGCAATGAT | 51429 |
| rs543397147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157763932 | CAGAGAGGATTTCTA[C/T]GGCAGTGGAAGAGAG | 51429 |
| rs543407961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157788073 | GTCTTCATAACAATC[C/T]TTGAATATTATTATT | 51429 |
| rs543419551 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157759563 | AGCTGGGCATGGTGG[C/T]GGGCGCCTGTAGTCC | 51429 |
| rs543428486 | snp | A/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157891813 | GAGGTGTGCAGATAA[A/G]AGTACAGTATAGTGT | 51429 |
| rs543439897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157845629 | TTTCCTGTGTATACT[A/G]GAGAGTATCCTGCAA | 51429 |
| rs543444675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157788671 | ACATAAAGTTTTGTC[A/G]AAAGGTTCACAACAT | 51429 |
| rs543463104 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | SNX9, LOC107986663 | GRCh38.p7 | 6:157714559 | TTATCCCTTGTGTCT[A/G]CACTGATGGATGTTG | 51429 |
| rs543496579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157717406 | AAGAAGCTTGTGCTC[A/G]GCTGGCCCGCCCTGC | 51429 |
| rs543540727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157844742 | GGGACTATAGGCACC[C/T]GCCACCACGCCCGGC | 51429 |
| rs543562010 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157899699 | GAATGGCCTGAACCC[A/G]GGAGGCGGAGCTTGC | 51429 |
| rs543564836 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888098 | GTTGTGTCATTCACA[A/G]CTGCGATTGGTAGGA | 51429 |
| rs543564897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157880416 | AGATTCCCTTATAAA[A/G]TGTCTCTCTAATCTT | 51429 |
| rs543578350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157852738 | CAGACCACCATGCCC[A/G]GCTAATTTTTGTATT | 51429 |
| rs543591893 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157826062 | ATCTTCAGATACAAT[A/T]TTCTTGTTTGTTCTT | 51429 |
| rs543619390 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157782551 | CAAAGAGGCAAAAAT[A/G]CTAGATGTTGTTATT | 51429 |
| rs543626011 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157881202 | TTCTTGCAATGTTTC[A/C]TACTTTTTCATCATT | 51429 |
| rs543626453 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157774368 | AGCATCTTTGTAAGT[C/G]GAACAGATGTGAGCA | 51429 |
| rs543639141 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157880809 | AGCCAGACTGTCTAG[A/G]TTTTAATCCCAGATC | 51429 |
| rs543659179 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157926291 | TTTGCTCCTTCCTGG[C/T]CTAGTTGGTCGTTAG | 51429 |
| rs543673560 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157873728 | ATTGTACAATAGACT[C/G]ACAGTTTAAATAGAT | 51429 |
| rs543723277 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157838534 | GAGACCCTCTGACCT[A/G]TTTCCCTCCATTTAG | 51429 |
| rs543729777 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157751597 | AAATGTGGTGTGTAC[A/C]TAAATGGAACACTAT | 51429 |
| rs543741778 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157872630 | CAACCCACATTAATT[C/T]GTATAGCGACTTGGG | 51429 |
| rs543788778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157853493 | TTATAGTTTTCACAA[A/G]TTGGAAATTTTTGAC | 51429 |
| rs543806836 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157761040 | TCGTATGAATCACTA[C/G]TTACACTTGGTGGTG | 51429 |
| rs543826807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894254 | AGCTGGGATTACAGG[C/T]GCCCACCACTACACC | 51429 |
| rs543831078 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157741866 | CATTTCCGGCGGAGA[G/T]CTTCCTTGCAAACTC | 51429 |
| rs543831535 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157902659 | TAAAACAAAAAAAAA[A/G]GTGTTGTGTTTTATT | 51429 |
| rs543836531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157897478 | CAAGGATTTTTACGG[C/T]GGTTTCATCACATAG | 51429 |
| rs543846458 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157917179 | GTTTTAGAGTTGCTC[A/G]TAGTATTTCTTTGTA | 51429 |
| rs543858991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157769741 | GTGTGGAGGATTTTT[A/G]GTGGAGGCCCATGTG | 51429 |
| rs543869195 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157724901 | CATTTTATATCAGGG[A/T]CGTGAGTATCCAAGG | 51429 |
| rs543879844 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157804494 | CCCTATAAACACAGG[A/C]AATCAGTAGTAGAAA | 51429 |
| rs543911425 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157807711 | GGTGTCATCCTGGGC[A/C]CACATGAGGCAAAGA | 51429 |
| rs543916078 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157802967 | GGTTGAAAATTACCC[A/T]TGTGAACCATACGTC | 51429 |
| rs543942196 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157765951 | CACCAAATTATCCTT[A/T]AAAAAAATCTTTTAA | 51429 |
| rs543947081 | in-del | -/AA/AAA | 0.330016 | 0.236849 | intron-variant | SNX9 | GRCh38.p7 | 6:157923428 | AGAAATTGAAAATCT[-/AA/AAA]AAAAAAAAAATAACC | 51429 |
| rs543952673 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157811702 | ATTTCATGCTTGGGG[G/T]TAGAACATGGTGATT | 51429 |
| rs543958480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157891112 | ACTCGGCTCACTGCA[A/G]CCTCCGCCTTCCAGG | 51429 |
| rs543965036 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157780164 | CTCCTAGTTCGCTGG[A/G]CTGCCTGGTGAGTAA | 51429 |
| rs543970668 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157767179 | AGCTGGAGGTATTTC[A/G]CTTGCTGGCACTTTA | 51429 |
| rs543975528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157939439 | AGTAAAAAAAAATCA[A/G]TCCTCAAGGGAGAAG | 51429 |
| rs543991938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157927796 | CAGTGGCACGATCTC[C/T]GCTCACTGCAAGCTC | 51429 |
| rs544006263 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157828810 | TCTAAGCATCACTTC[C/T]CCGGGAAAGCCTTTC | 51429 |
| rs544020538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157883864 | TATACAAATTATATT[A/G]CTTATTTGTAAATTG | 51429 |
| rs544031113 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157915840 | AAAAAAAAAAAAGAT[G/T]TATATGTAAGAATTT | 51429 |
| rs544060771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157738900 | TGGCTAGCCATATGC[A/G]GAAAACTGAAACTGG | 51429 |
| rs544060785 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157851815 | GCTGGTCTTGAACTT[C/T]TGACCTCAAGTGAGT | 51429 |
| rs544067495 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157747764 | AAATTACTAATCCCA[C/T]ATAAAGTATATTTAT | 51429 |
| rs544068339 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157846307 | ATATCCTTAAGCCTA[C/G]ATTTGTGCTGCATTA | 51429 |
| rs544071410 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157930675 | GAGAATCTAATGCCT[C/G]ATAATCTGAGGTGGA | 51429 |
| rs544100466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157752267 | CTCGTCGGGTGGGAC[A/G]AGAGACTGAGAAAAG | 51429 |
| rs544117240 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157898727 | ATTATTTTTTAACAA[C/T]TCCTGAACCCTGTCT | 51429 |
| rs544129874 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157765124 | TTAACAAGCCTATTA[A/G]GGTTAGAAAGAGACT | 51429 |
| rs544131288 | in-del | -/T | 0.425123 | 0.178415 | intron-variant | SNX9 | GRCh38.p7 | 6:157745244 | AGCAATAAAATCACC[-/T]TTTTTTTTTTTTTGC | 51429 |
| rs544141015 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157739652 | ACACATGCACATGTA[A/T]GTTTATTGAAGCACT | 51429 |
| rs544151028 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157849394 | TGTTGAGCACCTACT[C/G]TGTTCCAGGCATTGT | 51429 |
| rs544151681 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157875989 | CCACACGTTAAAAAA[A/T]AAGTTAAAAAAAAAG | 51429 |
| rs544185678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157755091 | CGACCAGAGGTCACT[C/T]TCGTGGCCATCTTGG | 51429 |
| rs544205720 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157848783 | CAGCAGCCGTAAAAT[A/G]ATAGGGGAAGGGTAG | 51429 |
| rs544214407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157719904 | TAGGCGTGGTGGCGC[A/G]TGCCCATAACTCCAG | 51429 |
| rs544232437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157800289 | TCATCTTAACTGACA[A/G]CCAAAAAATTATGAA | 51429 |
| rs544234445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157942321 | GCAAGAGGCCCTGGC[A/G]CAGAGACCACTGCAG | 51429 |
| rs544234513 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157942343 | CCACTGCAGCGCCTC[A/G]TTAGCTTCACAGGCA | 51429 |
| rs544269066 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SNX9 | GRCh38.p7 | 6:157823691 | TCTGGGCGCGGGTTG[A/G]GACCCCGGGCGCAGC | 51429 |
| rs544302168 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157830273 | GTATGTTGTTGGTAA[A/G]TCTCTTATATGTCTC | 51429 |
| rs544319206 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157854269 | CTATTTTAATTTGGG[A/G]GCTGGTGGTGAAGTT | 51429 |
| rs544319480 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157882673 | GTTCATGAAGGAAGT[A/G]ACTGCAGATGTGGTA | 51429 |
| rs544323988 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157916420 | ATGGGCCTTCTACTT[C/G]TGTTTCTGCCTTATT | 51429 |
| rs544337102 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157903939 | CTGTAGTGCTGTGAA[C/T]GATTTAACACCCTGT | 51429 |
| rs544349460 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157883390 | TCATCTCCTTGTTTA[A/G]GAAACTTCAGAGTCT | 51429 |
| rs544369081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157941884 | CCTCCCTTACAGGAC[A/G]TGGGCCCTATGCTCT | 51429 |
| rs544382044 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157830349 | AGCATTTTCTCCTAG[G/T]ACAATGAAGGTATTC | 51429 |
| rs544388597 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | SNX9, LOC107986663 | GRCh38.p7 | 6:157714781 | GGCACAGTGGCTCAC[A/G]CCTGTAATCCTAGCA | 51429 |
| rs544398410 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157836782 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 51429 |
| rs544408995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157938158 | TTTAAATGGATTCAG[C/T]GCCTCTTAAAAAATC | 51429 |
| rs544413501 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157876756 | CCTGAGCCTCATTGC[C/T]GTTTGAGGCCCCGCG | 51429 |
| rs544416155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157778603 | CATTTCTTGATCATC[C/T]ACTCTGCGTTAGACA | 51429 |
| rs544464144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157754709 | CTCTCACCTGTGCAG[C/T]TATCACAACCTCAAA | 51429 |
| rs544516659 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157809299 | TGGTGTCTTAGCAAC[C/T]GGATGTTTGCATACT | 51429 |
| rs544522442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157817513 | TCCATAAAGCAAGGA[C/T]ATGAGAGTGTGTCAG | 51429 |
| rs544525543 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157765979 | TAAAAACAGCTCATT[A/G]TCATCAAGACAATAT | 51429 |
| rs544539312 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157900157 | TTTTTTAGATTTTTT[A/T]AAAGACCTGTTAAAA | 51429 |
| rs544572803 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157867874 | CCTAAAGACAGTTAT[C/G]TATGTAATTGAGTTT | 51429 |
| rs544588172 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157920477 | CACCCTAGTGGTACC[A/C]CCATGTCGAACACGT | 51429 |
| rs544589794 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157913555 | CACTCTTTTTGGTGT[A/C]CAGTTCTGAGTTTTG | 51429 |
| rs544615565 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157870787 | CACATATATGCACTC[A/C]CCCGTGCAAGCACAC | 51429 |
| rs544623144 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157943041 | TCATTTCCGCATCCA[A/T]TATTTAAACCAGTGG | 51429 |
| rs544623868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157824306 | GTTACTTGATGTAGA[A/G]TAGCCACTGGGGAAG | 51429 |
| rs544627112 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157858518 | TGAGCCACCATGCCC[A/G]GCCATTGTCCAGAGT | 51429 |
| rs544634826 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157819686 | GAATCTAATTTTGAA[G/T]AAAAACACCTGGCCA | 51429 |
| rs544640093 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157903484 | CTCTGTCTTGTTAGT[A/C]AACTGTGTCTTGTTT | 51429 |
| rs544640444 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157865183 | GTCTCTACTAAAAAT[A/C]TGAAAATTAGCCAAG | 51429 |
| rs544651104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157913866 | TATTCCAGTGTTTAG[A/G]TATACCATAGCTTGT | 51429 |
| rs544657362 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157881431 | TATTAACCCTGCAGT[G/T]GCCTCTAAGTGTTTC | 51429 |
| rs544658457 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157829917 | GAGCCCACTCCCAAC[G/T]TTGTGGAAGGTTTGT | 51429 |
| rs544673687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157928422 | TAAAATATAAATCAG[C/T]GCTTTTTAAGTAGTT | 51429 |
| rs544682427 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157752422 | TACCATCTCAGACAG[G/T]GGGATGTGGCAGGAC | 51429 |
| rs544683315 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157837202 | TAGTGTTGTCAGTAA[C/G]TTTTCAGTTCTTTTG | 51429 |
| rs544718569 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157913491 | TTTCTAAAGGAAAGT[G/T]CAGGTTTCATTTTTT | 51429 |
| rs544723307 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157906348 | ATAACTGATAATATA[C/T]GTTAGTGTTGTAGGA | 51429 |
| rs544734600 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157741667 | CGTTAAAAATGATTA[A/C]GTCTGCAGTGCTTGA | 51429 |
| rs544758001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157813303 | TCAGCCACTGCAAAC[C/T]CCAAAAGGTCATATT | 51429 |
| rs544765831 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157781545 | TCTGGTAATAACTAA[A/G]TAGCTTAGTAAGACT | 51429 |
| rs544797865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157761983 | AGAAACTGGATGAAC[A/G]TCGCAGCAGGAAGGG | 51429 |
| rs544823614 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157898888 | GGACCAGGGGTGTGG[A/G]CTGGGTAGAAGCGTT | 51429 |
| rs544848702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157892147 | AAAGGACAGAGAGGC[A/G]CCACAGGATGGAAAC | 51429 |
| rs544851625 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157718149 | AGTTGTATTCCATGA[C/T]GTATGTATGTACCAC | 51429 |
| rs544861573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157726209 | TTTCCTGTTGGGTCA[C/T]CTCCGCCATTGTCTT | 51429 |
| rs544872897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157767668 | CAATGCAAGTTAAAC[A/G]GAACAATTTTGACTG | 51429 |
| rs544874823 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157858087 | GAGTTACTAACCCAG[C/G]CAGGTTCAGTGGTAG | 51429 |
| rs544878120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157725655 | GGGATGCAGGCCGCC[A/G]AGTGTCAGGGATACA | 51429 |
| rs544884736 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157836813 | AGCCCGGATGGTCTC[C/G]ATCTCCTGACCTCGT | 51429 |
| rs544897255 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157811917 | GTGTCACCCAAGGCT[A/G]CACTTATGTCAAGGC | 51429 |
| rs544906615 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157865617 | TTCAGACATGGAGAA[A/G]GGTTGGAATTGAATA | 51429 |
| rs544916644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157812655 | TCCAGTGAAGGCCCC[C/T]GAAGACTTTGGGGAA | 51429 |
| rs544917587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157901108 | CCTCCCTGACTGCAC[A/G]TCCATTCATAGGCTC | 51429 |
| rs544918615 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157820305 | AAAATAAAAAATAAA[A/T]AAAAACTTAGCCAGG | 51429 |
| rs544950065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157733024 | CCTGACACCCTCTAG[A/G]TTCATCTGTGTTGCT | 51429 |
| rs544955103 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157749248 | GACAGGGAGAGAGTT[C/T]GGGGAGATGGGTGAT | 51429 |
| rs544960097 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157768086 | GTCCCAGGTGAACTG[C/G]GACAGTTGGCCACCC | 51429 |
| rs544962039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157761434 | TCAAGAGCATTCTTA[A/G]AGACGCAATTTGTGT | 51429 |
| rs544962473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157861670 | GTCCCCCTTTAGTGA[C/T]GGGGGATATGTTCCG | 51429 |
| rs544972208 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157738758 | AAACAGATATATAGA[A/C]CAATGGAACAGAACA | 51429 |
| rs544973268 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157906576 | TTGTAAAGTACATGT[A/G]TGTTATCAGAATAAG | 51429 |
| rs544980150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157841474 | AGACCTACCTAGAGA[C/T]CCATGGGCCTTCATG | 51429 |
| rs544981244 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | SNX9 | GRCh38.p7 | 6:157827205 | TATATAATATATAAA[C/T]ATATATTATAGTTTA | 51429 |
| rs545034079 | snp | A/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885647 | GATAGGCCAGATGAC[A/G]TCATCACAGGTGGTG | 51429 |
| rs545040468 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157915937 | ATAGAGATCGCTTGA[A/T]TTTTGTATATCCACC | 51429 |
| rs545041814 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157874252 | CCATGCACACACCAC[A/G]GCCTTTTCCATACAA | 51429 |
| rs545046008 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157867372 | ACCGTTGGTGTTATT[A/C]TTCCTCAGAGTAGAG | 51429 |
| rs545072686 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157847308 | GGGTTTTGCCATGTT[G/T]CCCAGACTGGTCTTG | 51429 |
| rs545073462 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157917412 | ATATTTCCGCTATCA[C/T]AGGCATTAAATGCTA | 51429 |
| rs545082085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157880385 | TCTCTCACTATTCTA[C/T]CCTCTCTAATCGTGT | 51429 |
| rs545120537 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157872820 | CTTTTATTATCTGCC[A/G]CAGACCAGTACACAG | 51429 |
| rs545137047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157744807 | TGGAATGCAGTGGCA[C/T]GATCTCTGCTCACTG | 51429 |
| rs545138342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157840925 | ACTCGACTGGTGGCC[A/G]CATAGACATAAGCAA | 51429 |
| rs545143268 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157855062 | TTTCCTCAGGGGCAG[C/T]GTTACCCATTTCTTT | 51429 |
| rs545150463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157740680 | CAGTCAACAGGAGAA[C/T]GAATCCACAATTGTT | 51429 |
| rs545157814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157806032 | CACTCAGCCCACTGT[A/G]GTCTGTGAGTTGAAA | 51429 |
| rs545158158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157900520 | GCGAAAGCTGGGTCC[A/G]GGGGGGTCACTGCCT | 51429 |
| rs545164735 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157756824 | ATTCCGGCCAGCAGA[A/G]GGCAGGAGCGAGAGG | 51429 |
| rs545169685 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157795335 | GCAAGAGAATGGCTT[A/G]AACCCAGGAGGCAGA | 51429 |
| rs545172162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157759726 | TAAGAAAAATAAATA[A/G]AAGTTTAATGATATA | 51429 |
| rs545199171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157854479 | AATGTTAAGAGTATG[C/T]AAGCATATACTGTGA | 51429 |
| rs545211106 | in-del | -/TTTT | 0.299916 | 0.244966 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821598 | GTGTCACATATTTCC[-/TTTT]TTTTTTTTTTTTTAC | 51429 |
| rs545217937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157869385 | TTTCACAAGCACTTC[A/G]CACTGACCACGTCCA | 51429 |
| rs545227840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157805251 | TCATTGGTGTCCCAG[C/T]AGTCACCAATCGCTC | 51429 |
| rs545231115 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157875611 | GAGGCCCTCATCCTG[C/T]GAGTAGAAGCAGTGC | 51429 |
| rs545259550 | snp | A/G | | | synonymous-codon | SNX9 | GRCh38.p7 | 6:157867621 | AGGAGAAATCATCAC[A/G]ATCACAAATCCGGTA | 51429 |
| rs545265953 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157828944 | CAAGAAGCTGAGACT[C/G]TTTGTGATCACTTTT | 51429 |
| rs545282593 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157734627 | CTTATCATTATAGGA[C/T]TTATGGCTCTTTGTT | 51429 |
| rs545286310 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157777144 | CGCCTGTAATCCCAG[A/C]ACTTTGGGAGGCCAA | 51429 |
| rs545287367 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157775307 | AGGTTACAGTGAGCC[A/G]AGATCGCACCACCAC | 51429 |
| rs545289661 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157794865 | GAATATGAGATGCTT[-/A]AAAAAAAAGAGACTA | 51429 |
| rs545295056 | snp | A/G | 0.00438332 | 0.0466095 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157943034 | CTTTTGTTCATTTCC[A/G]CATCCATTATTTAAA | 51429 |
| rs545310647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157867814 | TGCTTATGAAATATT[A/G]ATGGTGAAGTAAGAA | 51429 |
| rs545311363 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157740031 | TGCAGCAAACCACCA[C/T]GGCACTTGTATACCT | 51429 |
| rs545322594 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157777527 | CTTTTAACTGTGTTT[A/T]CTGTTGTTTCGGTGA | 51429 |
| rs545334778 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157862287 | AAGTAAGTTCTGTTT[A/C]TTCTGATGATCTTAA | 51429 |
| rs545345851 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157865846 | AAAAGGGCCTTTCAA[A/G]TTCTTGCCATATGGT | 51429 |
| rs545360111 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157770604 | CACCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 51429 |
| rs545360161 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157764055 | GTATCATGCAAATGT[A/T]TACTTGCTTTGTGTA | 51429 |
| rs545382067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157748599 | CAGGGCATGGTGGTA[C/T]GCGCCTGTAGCCCCA | 51429 |
| rs545419232 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157882179 | TCCTTAGAATTATGC[A/G]GAATCTACTCTGCCT | 51429 |
| rs545421796 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157749387 | GGGATGAGGAAACCT[A/G]CCTCATGGAATCATT | 51429 |
| rs545429440 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157848838 | GATAGATACGTAACC[A/G]ATTTTGCACGTCATA | 51429 |
| rs545431970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157791864 | TATTGGTATGATTAT[A/G]AAGGAATCATTTAAC | 51429 |
| rs545442949 | in-del | -/TTTG | 0.00120144 | 0.0244801 | intron-variant | SNX9 | GRCh38.p7 | 6:157836116 | TTAATTTTTTGTTTG[-/TTTG]TTTGTTTGTTTGTTT | 51429 |
| rs545453001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157759190 | TTTGGCAACCTGGAC[A/G]TCAGAAGTCACACGG | 51429 |
| rs545460438 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157933414 | ATACTCAAGGCAGAC[A/G]GTGCTTTGGATGTCG | 51429 |
| rs545461118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157798625 | CACAAAAGTATTTAG[A/G]GGTGATAGGATATCA | 51429 |
| rs545462573 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157850506 | GTGGATGGGAGGAGT[A/C]ACCAACAGTCCCAGT | 51429 |
| rs545468298 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157870328 | CACCTACTCTCTCAC[C/T]TGCGCTCACACTCAC | 51429 |
| rs545496377 | in-del | -/T | 0.254385 | 0.249962 | intron-variant | SNX9 | GRCh38.p7 | 6:157730642 | TATGTCCCTTAGTTC[-/T]TTTTTTTTTTTTTTT | 51429 |
| rs545511429 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888486 | TTTCTGGAGAATTTG[G/T]TCCTGCCATGAATGT | 51429 |
| rs545516950 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157846092 | CTCCTGATGAGATTG[C/T]CTTCGGCTTCTCTGC | 51429 |
| rs545544905 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | SNX9, LOC107986663 | GRCh38.p7 | 6:157714590 | GTAATTTTCTGGAAT[A/G]TTGGGCTGAGAGGCA | 51429 |
| rs545545118 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157761143 | ACACTGCAGTGGTCT[C/G]CTTTCTATTATCGCC | 51429 |
| rs545549840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157870930 | TGCTGTCATGCACAC[A/G]CACACTCGCATGCTC | 51429 |
| rs545593615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157727633 | GATGGGTCCTGGCAC[A/G]AGGAGTGTAAGGCTG | 51429 |
| rs545599507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157915352 | ATTTTTATTGAAACC[A/G]CATTGATTCTGTAGA | 51429 |
| rs545609685 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157821047 | AAACAACAACAACAA[A/C]AAAAAACTTCTAGAA | 51429 |
| rs545617313 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157871652 | CTGCACGTTGTGCAC[A/G]TGTACCCTAGAACTT | 51429 |
| rs545626560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157908638 | CCTCTGCAGCTGCCC[C/T]CATGGCCTTGGATGC | 51429 |
| rs545650809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157835332 | TTTTTAAAATATTCT[A/G]ATATTTACTTCTATT | 51429 |
| rs545668673 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157906464 | ACTATTTTGATCATT[G/T]TTTTCTAAAGTGTCT | 51429 |
| rs545679926 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157736912 | TATTGAGATAATCAT[G/T]TAGTTTTTGTCATTG | 51429 |
| rs545689565 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157828586 | GCAGTCTCGACTTCC[C/G]TGGCTCAGGTGATCC | 51429 |
| rs545692024 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157730632 | AAATTTGACTTATGT[A/C]CCTTAGTTCTTTTTT | 51429 |
| rs545705093 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157742268 | CTGAGGAGAGGACAG[C/G]GGAAGAGTGTTTGGG | 51429 |
| rs545710208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157776495 | CAGGGGTGCAGCCCA[C/T]AGGTCCTTAAGTTTT | 51429 |
| rs545736254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157914595 | AGTCTTCCAGCCTCA[A/G]CCTCCTGAGTAGCTG | 51429 |
| rs545740174 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157922125 | TTTCATCACTGTAAT[C/G]GTGAGTCCAGAGTCA | 51429 |
| rs545747506 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157838164 | ACTACAGGCATGCAT[C/T]ACCATGCCTGGCTAA | 51429 |
| rs545755217 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157884081 | TGTGTTCTTAACACC[A/G]ACCACAGGCCTAGGA | 51429 |
| rs545763427 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157716404 | AATAGCCCTAGGTCC[A/G]CTGGATGGACAAGAA | 51429 |
| rs545774286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157899053 | GGCCGTTAGAGTAGG[A/G]GAGGAAGGAGAAGGA | 51429 |
| rs545774296 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157769569 | GATTCAGGCAGAGGG[G/T]GTCACCTGTAAGGAG | 51429 |
| rs545784158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157831105 | TTAAGCTTCTCTTAA[A/G]CATGTCAAAACATTA | 51429 |
| rs545787492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157794321 | GGCCTCCCCAGCCAC[A/G]TGGAACTGTGAGTCT | 51429 |
| rs545790292 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157803346 | AACAAAAAAGAGAGC[A/G]TGTGAAGGGAAAGAG | 51429 |
| rs545793954 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157787175 | CTGCCTTGGAAATGG[A/T]ACAACAATTTTTTTC | 51429 |
| rs545841463 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157834346 | GCTAATTTAAAAGAA[-/T]TTTTTTTTTTTTTTT | 51429 |
| rs545844318 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157897225 | AGTCAGATCAAGGGG[A/G]TTCCCACCACTCCCA | 51429 |
| rs545854557 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157930043 | GAGTAGTTTCAACAG[A/G]AACTTGTGGCTCCAT | 51429 |
| rs545857565 | snp | C/T | 1.65861e-05 | 0.00287972 | intron-variant | SNX9 | GRCh38.p7 | 6:157937390 | CTTTTCCTTGATTTT[C/T]TGAATTTCTCTGCCA | 51429 |
| rs545871428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157809903 | TGGAACAGTATGTCA[C/T]GTTATTATATAGTTA | 51429 |
| rs545873388 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157866419 | TCTCTACAAAAAATA[C/G]AAAAATTAGCTGGGC | 51429 |
| rs545884835 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157892530 | ACCACAAAGATTTCA[C/T]AACTTAGGTGGAGAG | 51429 |
| rs545901366 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157801752 | TAAAAAAAAAAAAAC[A/C]CACAAAATATCCATT | 51429 |
| rs545907674 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157926395 | ATATTTTTAAAAAAA[C/T]AGCTCATAATACTGG | 51429 |
| rs545910183 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157919775 | GGTTCATATCTTGCT[A/G]TTTCTTTGCGTATCT | 51429 |
| rs545921881 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157867818 | TATGAAATATTGATG[C/G]TGAAGTAAGAAGCTG | 51429 |
| rs545931553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157911843 | AGAAGTTTTGATTTT[A/G]ATTTTTTTGGAACAC | 51429 |
| rs545944990 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157878868 | CTCTTGCTAATCTGT[A/T]AGAAAAAGATGAAGA | 51429 |
| rs545957573 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894165 | CCCAGTCTGGAGTGC[A/G]GTGGCGTGATCTCAG | 51429 |
| rs545961262 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157911070 | GTGAGCCGAGATTGC[A/G]CCACCGCACTCCAGC | 51429 |
| rs545973328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157831888 | GCAGACTGTCAAGTG[A/G]AGGGAGTGGAATATG | 51429 |
| rs545995611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157780244 | AACATTTACTAACCT[C/T]AACAGGATGTTGTGG | 51429 |
| rs545998406 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157789532 | CCGCTGTAGACGGCA[A/C]ACTCTACTGTAGAAG | 51429 |
| rs545998938 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157905037 | AATTCCCTTATCACC[G/T]TAGAAGGTAGGTCAT | 51429 |
| rs546011733 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157918185 | TTCTTTCTAGTTCTA[A/T]CAATTATTGAGTATC | 51429 |
| rs546011780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157824502 | CTACTTTTGGGTTGC[C/T]AGAAACGTTATTTTT | 51429 |
| rs546052741 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157825289 | GAAAAAAGAGAAGAC[A/G]GTTTATGACATAGAG | 51429 |
| rs546056172 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157722293 | CGGCAGGGTAAAAAG[C/G]ACTTCTTTTGTTATC | 51429 |
| rs546057872 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157799874 | TTGAGATTTGGGTGG[A/T]GACATAGTCAAACCA | 51429 |
| rs546079311 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157926481 | ATATTTGAGGCACTA[G/T]GTCAGAATGCATAGG | 51429 |
| rs546085678 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157838828 | TACTCTAAAATTTTA[C/T]CTGGCACTGGTTAAA | 51429 |
| rs546096711 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157774025 | ATGAAGAAAGCGTCT[A/G]GACTGAACAGACGAG | 51429 |
| rs546107827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157752196 | ACTTTGTCTCAAAAA[A/G]AAAAAAATTAACAGG | 51429 |
| rs546114075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157879647 | TCAAGAGTATTTCAC[A/G]TTAGTGGCTGAACCA | 51429 |
| rs546114785 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157751107 | TACCCAAGACTGGGA[A/G]GAAAAAGAGGTTTCA | 51429 |
| rs546141240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157917488 | CCTTATTGAGTTTTC[A/G]TGTTCATTCAGGTCA | 51429 |
| rs546172504 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157895156 | TAGCATTAAAATGAG[G/T]TGGAATTGGGCTCTT | 51429 |
| rs546182287 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157739947 | ACACCAGGGCCCTGT[A/C]GGGCGGTGGGAGCCT | 51429 |
| rs546183337 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157879646 | TTCAAGAGTATTTCA[C/T]GTTAGTGGCTGAACC | 51429 |
| rs546184519 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157763525 | CGGAAGCAAGTCAGG[C/G]AGGGAGCCAGGAATG | 51429 |
| rs546185901 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157859972 | AAATCTAGCCTGTCA[G/T]GTGCAGTTTGTAAAT | 51429 |
| rs546199254 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157741919 | AGGTCCCACCTGGCC[C/T]CATCATTCTGTCAAT | 51429 |
| rs546206128 | in-del | -/TATTT | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157737056 | GGTTTGGTTTGCCAG[-/TATTT]TATTGGGGATTTTCA | 51429 |
| rs546208401 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157899589 | CATCCTGGCTAACAC[A/G]GTGAAACCCCATCTC | 51429 |
| rs546226322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157811643 | CTTTGTGACTCCACA[A/G]GGAACTCATGTTTTA | 51429 |
| rs546227323 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157852013 | CCTTTGTATTTTGTT[A/T]ATTCATCCGTTGATG | 51429 |
| rs546256202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157759398 | TTAAACACAGCCATT[A/G]TTAAAAATTAAATGG | 51429 |
| rs546293879 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157912486 | GCAAGAAAGCAGCAG[C/T]CCCTCGGTGTGAAGA | 51429 |
| rs546314429 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157804870 | GAGCCCGCCTTTACT[A/G]CGGTAGGGAGGAGCA | 51429 |
| rs546344121 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157942525 | CAGGTGGTCTGGAAG[C/T]GCCGCTAGGGCAGAG | 51429 |
| rs546354575 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157807526 | ATTATTTAAAATGCA[C/T]AGCTGAGCTCAAAAG | 51429 |
| rs546355114 | in-del | -/AAACA | 0.0123036 | 0.0774623 | intron-variant | SNX9 | GRCh38.p7 | 6:157865025 | GAGAGACTCTGGCTC[-/AAACA]AAACAAAACAAAACA | 51429 |
| rs546361735 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157792133 | TCCTTCCTCCCTCCC[G/T]GCCTTCCTTCCTTCC | 51429 |
| rs546366504 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157943962 | GTACAGAGTCCCCGG[C/T]GCTCTGAGGTTGGAG | 51429 |
| rs546367987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157828345 | GTTTTTATATTGACC[A/G]TCTGAAAATTAAATT | 51429 |
| rs546368584 | in-del | -/CTGT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157772082 | GGAAGAGTAGGGGTG[-/CTGT]CTGTCATGGTCATCT | 51429 |
| rs546384510 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157830803 | TATTCATGAAAATTG[C/T]CTTTTCTCCATTCTT | 51429 |
| rs546392406 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157921813 | CCTAAATCCCCACCA[C/T]AGGAAATTTGTCATG | 51429 |
| rs546407119 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157751371 | CAGGAGTATAGTTCA[A/G]GATGAGATTTGGGTG | 51429 |
| rs546412115 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887394 | CCTGACCTTGGGTAG[A/G]CCCCTCACGTGATGG | 51429 |
| rs546413512 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157846164 | TCTGTCAGCTGCTGT[G/T]AGGCAAAATCTCTTC | 51429 |
| rs546415855 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157786658 | AAACTATAAGACAAT[A/C]AATTTTTAAATTTCA | 51429 |
| rs546419885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157764903 | CATCTCTTGCAAAGT[A/G]TAATTACAGATCCCT | 51429 |
| rs546442343 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157723969 | TCTGCTGATAACTTC[C/T]GGAGTAAGCACAGAC | 51429 |
| rs546454273 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157856277 | GCCAAACACATTCAG[A/G]AGTAGAAGAGTATAA | 51429 |
| rs546458683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157835564 | ATATGGTTAGGCTTC[A/G]TGTCCCCACCCAAAT | 51429 |
| rs546503622 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157740253 | CTGTGCCCATAGAAT[C/G]TAATATACTGGTTTC | 51429 |
| rs546525106 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157921088 | AATACCATGTCGTTT[G/T]TAAGAATGACATTAA | 51429 |
| rs546525189 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157928962 | TTTGGGGCTTTATAA[C/T]CTTTGGAAAATTAAT | 51429 |
| rs546541398 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157727741 | GGGCATCAATTTCCC[A/T]GGGTTTAATTATTAG | 51429 |
| rs546552457 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157845545 | ATAATTCAGTTGCAT[A/G]GCTATAGTAACTTAC | 51429 |
| rs546552564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157935548 | AAGGGGCCGAGGGAG[A/G]AGAATCCACAGAGTT | 51429 |
| rs546586436 | snp | G/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822044 | GGCCGTCAATGAATG[G/T]TGGCCTCCCAATATT | 51429 |
| rs546587355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889283 | TAAAAATACAAAAAT[C/T]AGCTGGGTGTGGTGG | 51429 |
| rs546591626 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | SNX9 | GRCh38.p7 | 6:157847196 | CAGCTTCCACCTCTT[C/G]GGCTCAGGTGATCCT | 51429 |
| rs546597302 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157752645 | TGGAATATACAATCG[C/G]GTTTTACACCGAGAC | 51429 |
| rs546620549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888723 | CTAAAAGTCATCTTT[C/T]TTTCCCAAGTGAAGT | 51429 |
| rs546630027 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157730019 | TGGAATGGGTGTGGG[A/G]GCGGGGAGTTGGGGC | 51429 |
| rs546659984 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157828746 | CCGCAAAGTATTGGG[A/T]TTACAGGTTTGAGAC | 51429 |
| rs546669323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157908918 | GGAGGCCTACCCTCT[C/T]CAGGCAAGCCTTGCC | 51429 |
| rs546688858 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157837194 | CCAACTTGTAGTGTT[A/G]TCAGTAACTTTTCAG | 51429 |
| rs546690825 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157810663 | TGAAATCTTCAGGAA[C/T]GGAACCCTTGATGTT | 51429 |
| rs546697125 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821243 | GTGCCCAGGATGACT[A/G]TTTGCATAGGATTTG | 51429 |
| rs546708044 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157898118 | GCCGGGAACTAGGGA[C/T]GCAGACCAGATGGCT | 51429 |
| rs546714761 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157758688 | ACTGGGCACATGGTG[A/T]CACCATGTCCCCTGG | 51429 |
| rs546762216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157854558 | CAAACACGTATGGCA[A/G]ATTTATAACATTTTG | 51429 |
| rs546762328 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157846986 | TGGGAAGTGGAGAAG[A/T]GAGCCCAGGTAGCAC | 51429 |
| rs546786695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157874652 | AAGCTTACATGGAAC[A/G]TTCTCTAAGACAGAC | 51429 |
| rs546806407 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157915672 | ACACACACACACACA[A/C]AAATTAGCCAGGCGT | 51429 |
| rs546816461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157734060 | TATTATTTTAAGATA[A/G]TATAATAATATTTTA | 51429 |
| rs546828438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157841147 | GGCTAAGAAGAAATG[A/G]CATCATCTTGGCTTA | 51429 |
| rs546851959 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157926230 | AAGGGAAGAGGTAGC[A/G]GTGTTTGGGGAAAGG | 51429 |
| rs546854041 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157875261 | TGATGCATTATAGCT[A/C]TTGCCATTCCCCAAA | 51429 |
| rs546879525 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157881703 | GTGGTCTGGGTAGAA[C/G]ATCAAACAGGCCACA | 51429 |
| rs546915976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157835072 | GGCTGGAGTGCAGTG[A/G]CATGATCTCAGCTCA | 51429 |
| rs546917613 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157746102 | TTAGAATGTTGGAAT[G/T]GATCAATGGCATCCT | 51429 |
| rs546920432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157721351 | ACACCGGAATGCAGC[A/G]TCATGCTAATCTTAA | 51429 |
| rs546924403 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157816982 | GAGCTCTCATGATTG[A/G]AGTTATGCCTTATAA | 51429 |
| rs546955277 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157792454 | GATTTTTTATTTTTT[A/T]ATTGACAAAAATATA | 51429 |
| rs546960939 | snp | G/T | | | downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157945128 | CGTGGTGGAAGAAAA[G/T]GTCAGTCTCGTTGTC | 51429 |
| rs546969359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157814922 | AATATGCTAACTTAG[C/T]CTGTAATTGCCAAGT | 51429 |
| rs546978913 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888343 | TAGTTATTTTTAGGG[-/T]TTCATTAATACTGTA | 51429 |
| rs546991020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157765609 | ATCCGCCCGCCTCGG[C/T]CTCCCAAAGTGCTGG | 51429 |
| rs547002870 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157723555 | TGGGTTTTTCCCTCC[C/T]ATGCCAAATCTATCA | 51429 |
| rs547004835 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157731251 | ACGTGCCTCGCTCCT[C/G]AAGTGCTGGGATTGC | 51429 |
| rs547007511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157806559 | GTATCCTACCGTCTA[C/T]CAAATAATCTTAAAA | 51429 |
| rs547009291 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157858859 | CTTACTCACTACCAC[A/G]AGAACAGTATGGGGG | 51429 |
| rs547014493 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157770554 | GCACTTTGGGAGGCC[A/C]AGGCGGGCAGATCAC | 51429 |
| rs547034599 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157771994 | GTGAGGCACTGCACC[C/T]GGCCCGGCAGCCAAA | 51429 |
| rs547037718 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157914871 | CATGGACTGTGCTTG[A/C]GGTGTCATGGCTAAG | 51429 |
| rs547072017 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157817798 | GAGAATTGCTTGAAC[C/T]CGGGAGGCAGAGGTT | 51429 |
| rs547104665 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157775481 | CTTTCTCCTCCAGGC[C/T]AGTCGTATGCCAGGA | 51429 |
| rs547142928 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157756424 | CTCTGTCTAAAAAAA[-/C]AAAAAAGAGTTAAAT | 51429 |
| rs547145311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157917708 | TTTAAATCATCTCTA[A/G]ATTAATTATAATACC | 51429 |
| rs547146407 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157771652 | TGTCGCCCAAGATGC[A/G]CGCAGGAGGAGCTGC | 51429 |
| rs547153586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157736519 | TGTATCCTGAGACTT[C/T]GCTGAAGTTGCTTAT | 51429 |
| rs547174139 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157871199 | AGCCTTAGTAACATG[C/G]CAAAACCTCATCTCT | 51429 |
| rs547184769 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157929638 | ATATTTTGAATTATG[A/C]GTAACATATACCTAC | 51429 |
| rs547194288 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157852799 | GGCTGGTCTTAAATT[C/G]CTGAGTTTGTGCGAT | 51429 |
| rs547195718 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157897598 | CTGCAACCTCCGCCT[C/T]CCAGGTTCAAGTGAT | 51429 |
| rs547207221 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157911393 | AGACAAGAGGCGGTG[C/G]AATTCTCACTGCACT | 51429 |
| rs547210872 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157884098 | CCACAGGCCTAGGAG[A/C]TGTCCATCACTGGCC | 51429 |
| rs547215284 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157883181 | GAAGGCTCAGATGAT[C/G/T]GTTAGCGATTTTTAG | 51429 |
| rs547221398 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157760073 | AGATGGGGTTTCACC[A/G]TGTTGGCCAGGATGG | 51429 |
| rs547226070 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157728688 | GCTATTTACAGCAGG[C/T]GAAACAGTTCCTTCT | 51429 |
| rs547227570 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157939129 | GTCATTTTAGGCACA[A/T]TTTTTTTGTGTCAAG | 51429 |
| rs547228072 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157749337 | TGGGAAAATTATTTA[A/C]CTTTTGTGGGCCTCA | 51429 |
| rs547260405 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893187 | TCTTAGCTGAAGTGT[A/G]ACTGCCAGGCCCTCA | 51429 |
| rs547263273 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157793027 | CTCAGCTCACTGTAA[A/C/G]CTCCACCTCCCGGGT | 51429 |
| rs547265119 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157801086 | CTTTCTTTGGGCGTA[G/T]GACTTCAGGTGAGGT | 51429 |
| rs547286416 | in-del | -/TC | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157931801 | TGGGCAAGTCAGTTA[-/TC]TGAGCCTTATTTTCC | 51429 |
| rs547328601 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157762300 | TTCCTTCTATGAAGG[A/G]AGGTGGTAGAAAGCC | 51429 |
| rs547332175 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157852275 | TATATCTGAATTTTA[C/T]ACATACTCCAAAACT | 51429 |
| rs547360454 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157755531 | TATTTTGTCAAAGAT[A/T]AAAGAAAGAAAAGGC | 51429 |
| rs547423949 | snp | C/T | 0.494533 | 0.0519972 | intron-variant | SNX9 | GRCh38.p7 | 6:157873072 | AACTGTAATCTTTTT[C/T]TTTTTTTTTTTTTTT | 51429 |
| rs547478325 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157919291 | ACTATGCATGATCAG[C/T]CATTCAGATATTTTT | 51429 |
| rs547501547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157918416 | TAATATTAATATAGC[C/T]ACTCCATTTCTGTTA | 51429 |
| rs547509811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157737255 | TTGTACCTCTGGTAT[A/G]ATTCGGCTGTGAATC | 51429 |
| rs547521009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157754163 | TAGCCTCCAGCTGCA[C/T]GACTCCTAAATCATA | 51429 |
| rs547531612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157839566 | TGTGAATTCCATTGC[A/G]CAGTCCAAGTGGGGG | 51429 |
| rs547533321 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157751740 | TACTTAACGGAGGTA[A/T]CTAAAATATTTAAAT | 51429 |
| rs547558193 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157789150 | AGTGAGCCGAGATAG[A/C]GCCACTGCACTCTGG | 51429 |
| rs547572658 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157773359 | CACAGAGGCAGCCGA[G/T]GTGCAGAGGTCACAT | 51429 |
| rs547575446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157803305 | GATCTATATGAGGAA[A/G]TACTTCACATATTTT | 51429 |
| rs547580903 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157914688 | TCACCCTGTTGCCTA[G/T]GCTGGTCTCGAAGTC | 51429 |
| rs547593516 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157899769 | ACAAAGCGAGGCTCC[G/T]TCTCAAAAAAAAAAT | 51429 |
| rs547602598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157770548 | ATCCCAGCACTTTGG[A/G]AGGCCAAGGCGGGCA | 51429 |
| rs547625259 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157744103 | AAATTAAATGATGCA[A/T]TGTATATAAAACAAC | 51429 |
| rs547642066 | snp | A/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886684 | CTAGTTAATTATGTC[A/G]AATTCCAATTTGGAA | 51429 |
| rs547658502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157796189 | TTCAATATAAATATG[C/T]TCGCAATGCTGTTTC | 51429 |
| rs547675082 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157774612 | GGGTCTCCTTCCTCT[A/G]GCATACTTGGGGGAA | 51429 |
| rs547683784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157873888 | GGGCTGGTCCTGCCT[A/G]GGACACCCCCAAGCT | 51429 |
| rs547694396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157811187 | TCCTTGAAGTGAGTA[A/G]AGATGCAACTAACAC | 51429 |
| rs547715624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157770088 | AGCTGATCCTGCCCA[A/G]GGCTGAACGTTTTCC | 51429 |
| rs547729721 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157926737 | GTGAGCTGAGATCAT[-/G]GCCACTGTACTCCAG | 51429 |
| rs547735493 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157843351 | GCCTGCTGTTGACTG[A/G]AAGCCTTATAACGCA | 51429 |
| rs547740980 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157789808 | GGCAGCTTTTACATC[C/G]CTTAGGATTAAGTCC | 51429 |
| rs547743265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157834087 | TGACTGGATCCTGCC[A/G]TGGGGTGACACCAGG | 51429 |
| rs547756797 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157883130 | AAAACAAGACCCCCC[C/G]GCCACCCCAGCAAAA | 51429 |
| rs547764037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157782744 | AGACAAAAATTAACC[A/G]GGCGTGGTGGCATGT | 51429 |
| rs547767915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157867155 | ATGGAATCTCGCTTT[A/G]TTGCTCAGGCTGGTC | 51429 |
| rs547789897 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157911316 | ACTGAGATGCTCACC[G/T]GAACCTAGGGAGAAG | 51429 |
| rs547816650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157876259 | GAGTTTGAGACCATC[C/T]TGGCCAACATGGTGA | 51429 |
| rs547833265 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157778847 | GCAAAAATGTGATGC[A/G]AGTGCTATGAGTATG | 51429 |
| rs547837555 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157845690 | ATACAAAGCATAGAC[A/G]GCATTGGTGAATCTG | 51429 |
| rs547842766 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157754011 | CTTGTGCTGAATCAG[G/T]TCCTAGGTGGGAGCC | 51429 |
| rs547845341 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157792882 | TCACTTCCAGCTATT[G/T]TTCATATATCCACCC | 51429 |
| rs547845540 | in-del | -/A | 0.00914312 | 0.0669923 | intron-variant | SNX9 | GRCh38.p7 | 6:157728219 | TATGCCCTTCACCCT[-/A]TGAATCCCCCAAAGA | 51429 |
| rs547847401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157933429 | AGTGCTTTGGATGTC[A/G]GTTTCTGAATATTTT | 51429 |
| rs547863373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157747314 | ACACAAACACACAAG[A/G]TATTTTCACTGAATG | 51429 |
| rs547880394 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886767 | AGAAGTTATTTTATA[C/G]CTACTACAAATAGTG | 51429 |
| rs547885411 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157824832 | TTTTGTGTTGACCTT[C/T]TTAAAAATAAAACTT | 51429 |
| rs547895114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157796760 | GTATCTATTACACAC[A/G]GGCACTATTCTAGGT | 51429 |
| rs547904916 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157775855 | GAAAAGGAGGAGAAA[A/G]GTGGAGAGTCATGTT | 51429 |
| rs547915002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157839952 | TTTGGATTCTCCTAT[C/T]CTCTCCGGTTGTTTC | 51429 |
| rs547927608 | snp | A/G | 1.66996e-05 | 0.00288956 | intron-variant | SNX9 | GRCh38.p7 | 6:157867516 | TCTGTTTGTGTTTGT[A/G]ACATCCTCTTTTCCT | 51429 |
| rs547944290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157848847 | GTAACCGATTTTGCA[C/T]GTCATAAAATGCTTC | 51429 |
| rs547957007 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | SNX9, LOC107986663 | GRCh38.p7 | 6:157714956 | GCTGAGGCAGGAGAA[C/T]TGCTAGAACCCGGGA | 51429 |
| rs547966534 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157819928 | GTAATAACCAAACGC[A/C]GTCTGCAAATGCAAA | 51429 |
| rs547967917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157895819 | CAGACCAGGCCAAAC[C/T]AGAATGGAGTTCCTT | 51429 |
| rs547971159 | snp | A/G | 1.64841e-05 | 0.00287085 | intron-variant | SNX9 | GRCh38.p7 | 6:157909858 | CTTGCTTTTTTCTTC[A/G]TTTTCTAGAGTTGGC | 51429 |
| rs547989386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157772473 | CCAAGTGAAAAGGGA[A/G]GCAGAGAGTGGGGTG | 51429 |
| rs547990898 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157861947 | TCTACTAAATGGGAC[G/T]GCTACTACATGACAG | 51429 |
| rs547992280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890154 | TAAACTCCACCTAGT[A/G]TACCAGGATTCGTCT | 51429 |
| rs547997837 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157770216 | AGGGAGGCTCACAGC[A/G]CCCAGCTCAGGGCCG | 51429 |
| rs547998807 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157847246 | TAGCTGAGACCACAG[A/G]TGTGCACCACACTGC | 51429 |
| rs547998926 | in-del | -/TT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157859810 | GAGTTCCAGAAACTC[-/TT]TATGTATCAGAAGAT | 51429 |
| rs548005236 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157812887 | AGATAGGAAATACAC[C/T]AATAGAATGGAATCT | 51429 |
| rs548008097 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157718364 | ACTCTCCAATTTTCC[A/G]CAGAGGTTGTACTAA | 51429 |
| rs548012670 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157763339 | AGGAGTTTTCCCCAT[-/G]GATCTCCAGGCCTTC | 51429 |
| rs548022566 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157725853 | CACCCAAGAAAATCC[A/T]CCACATACACTACCC | 51429 |
| rs548029833 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157898039 | CAGAGACCAAATATC[A/C]GAACAAAAGATACAC | 51429 |
| rs548032974 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157870050 | AGGCAGCACTCACAC[A/G]TGTGAGCACGCACAC | 51429 |
| rs548043450 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157738532 | GAGCCTATGTGTGTC[G/T]TTGCACATCAGATGG | 51429 |
| rs548070314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157876770 | CCGTTTGAGGCCCCG[C/T]GCCCTTTCCTAGTGG | 51429 |
| rs548072128 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157908091 | TCCCATCTTCCTCTT[-/A]AAAAAAAAAAATTAG | 51429 |
| rs548082117 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822955 | GGGCGGCCACGCAGG[G/T]TTGCGGGCCATGGCC | 51429 |
| rs548086677 | snp | A/C | 0.00159617 | 0.0282053 | downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157945554 | GTCTGTGGGCACCCC[A/C]CATCCCCCCGCCCCC | 51429 |
| rs548087602 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157870325 | ACACACCTACTCTCT[C/G]ACCTGCGCTCACACT | 51429 |
| rs548098213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157913635 | ACAGCTCCGTCACCT[C/T]CCCAGGTTCCCTCGT | 51429 |
| rs548098656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157864677 | AGCCCGTCCCCTGCC[C/T]GCATTTCTGTCCTGT | 51429 |
| rs548118984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157827639 | ATTGTCAGTCATCCT[A/G]TTTTATTTAAAAGAT | 51429 |
| rs548122346 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157816252 | ATCTGTGTTTCTAAA[C/G]AGTCATTTACTTAAT | 51429 |
| rs548147346 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157732279 | TTCTAACATTCTGCC[C/T]CAGGCTGCATTTACT | 51429 |
| rs548157809 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157740935 | TCAGTTTCAAAATGG[A/T]GGGAATGACATCTAC | 51429 |
| rs548169368 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157922847 | GTCATGTAGCTATAT[A/G]GTAGTGAAACTAAGT | 51429 |
| rs548221279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157801831 | GAAAGAACTGCTTGT[C/T]ATGTCAAAGGTGGCT | 51429 |
| rs548226898 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157841802 | ATGATAAGAATTTAC[G/T]ACACTGTGACTTTTA | 51429 |
| rs548227409 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157910484 | AGAAGCCACAGAACT[A/C]CTAAGTGTTAATGAA | 51429 |
| rs548236860 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157876317 | ATTAGCTAGGTGTGG[C/T]GGCAGGCACCTGTAA | 51429 |
| rs548289542 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157800407 | CCCTGGGAGGCTGCG[G/T]CAGGTGGATTGCTTG | 51429 |
| rs548291200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157903533 | TTTCAGTCATGGTCA[A/G]TAGTGATGTGCATCA | 51429 |
| rs548295205 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157808520 | CTAACAAACCACTGT[A/G]TGTCTGTTTATGATG | 51429 |
| rs548318826 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157778895 | TATGTTGTAGAGGAT[C/T]AACATCACCTGTCTG | 51429 |
| rs548323732 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157807183 | TCCTGCACAGTTATA[A/G]GACAAGGACTCTATT | 51429 |
| rs548344181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157929461 | TGCCTTTAACTCCCT[C/T]AGAGTCCTAGGACTT | 51429 |
| rs548357800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157830779 | CAGCTCTAGAAAATT[C/T]TCAGCGGTTATTCAT | 51429 |
| rs548358758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157728600 | CCCTCAAGGTTAGAT[C/T]GTCCCTACCATTCCT | 51429 |
| rs548376310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157925086 | TTCAGCCATGACAAG[C/T]GAAAAACAAGCTACT | 51429 |
| rs548414995 | snp | A/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887110 | TGCTATATGCTGGAT[A/G]TTTTTGCATTCCCAT | 51429 |
| rs548423195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157721340 | TTGTCCCAAGCACAC[C/T]GGAATGCAGCGTCAT | 51429 |
| rs548429083 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157760913 | AGAGGGCAGGCTGGG[A/G]AAGGCAGTGTCTGGC | 51429 |
| rs548461503 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157869616 | AAGCTCTCATCCTCT[G/T]GCCTGGACCATGCAC | 51429 |
| rs548464412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157787446 | TCTCTCCCCCCCACC[C/T]CTCTCTCTGTGTATA | 51429 |
| rs548470959 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157815373 | TCCAGGCACATGCCA[C/T]CACGCCTAGCTAATT | 51429 |
| rs548473278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157741332 | AGTCTGGGTAACACA[A/G]CGAGACTCTGTCTCA | 51429 |
| rs548476641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157836827 | CGATCTCCTGACCTC[A/G]TGATCCGCCCACCTT | 51429 |
| rs548483831 | snp | A/G | | | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157943914 | ATTAGATGGAAAAGT[A/G]TAGGGACTGAGAAGG | 51429 |
| rs548509786 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157932027 | TCAATTAAAATAATC[A/G]AAAGAAATCAATTGA | 51429 |
| rs548509916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157924687 | TGTAAGCCGAAGTAA[A/G]TCCCTACTGAAATGG | 51429 |
| rs548514407 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157830050 | AGGTTATTTAACTCC[A/C/G]GTCATCTCCCCCAAT | 51429 |
| rs548527945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157804209 | GAATGTATTAGAAGG[C/T]TGTTGAGAGTTTACT | 51429 |
| rs548544475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157734854 | TCCCTTACAGTATTA[C/T]GTTCAAAGAAAACAG | 51429 |
| rs548560657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157812820 | GTAATAGACAATATA[C/T]TATAAGATATTATAA | 51429 |
| rs548583717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157794473 | TTCACAGTAAAGGCA[A/G]GGCTAAAGCCAAGTC | 51429 |
| rs548593462 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157831094 | TGCTCATATTTTTAA[A/G]CTTCTCTTAAGCATG | 51429 |
| rs548598387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157804841 | GATGTGAGCTGGAGC[A/G]TGGAGGGAGGGAGGA | 51429 |
| rs548607658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157850679 | AAAAATTTGATAGTG[A/G]TGTTTCATTGTCAAG | 51429 |
| rs548624095 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157755321 | TGACACCGGGAGAAA[G/T]TCTCCCTCTCAGCCA | 51429 |
| rs548628530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157913613 | CCACTACATTTCATG[A/G]TACAGAACAGCTCCG | 51429 |
| rs548641946 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157865285 | CAGAGGTTGCAGTGA[C/G]CCCAAATGGCATCAC | 51429 |
| rs548645539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157837810 | AGAAGGGCAGCAGAT[C/T]GTGAAGCCGTCGTTG | 51429 |
| rs548651840 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157942514 | CTGAGGAAAAGCAGG[G/T]GGTCTGGAAGCGCCG | 51429 |
| rs548677917 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157897692 | GCTGATTTTTTGTAT[A/T]TTTATTAGAGGCAAG | 51429 |
| rs548681003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157857538 | TCATTTTTTTCCTTC[A/G]GATAGTTACTTATTT | 51429 |
| rs548686389 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157817039 | CTTCCACCATGTGAG[C/G]ACATAGCGAGAAGAT | 51429 |
| rs548691987 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157906460 | ATATACTATTTTGAT[C/T]ATTTTTTTCTAAAGT | 51429 |
| rs548711533 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157717682 | TGAAAAAGTAGGTCA[C/T]GTGCAAGGAACTGAG | 51429 |
| rs548746087 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157838331 | AATTTTTTTTTTTTT[A/T]ATTCAACAGTCTCTC | 51429 |
| rs548752706 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157834361 | ATTTTTTTTTTTTTT[G/T]GTAGAGACGGGGTCT | 51429 |
| rs548759572 | in-del | -/ATAG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157742096 | TGGCCTCCAGCAGTA[-/ATAG]ATAGCACTGCTAACT | 51429 |
| rs548775772 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157923173 | GAGTTCTGGTCTTAG[G/T]GCCACTTCTAGCTGC | 51429 |
| rs548776753 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157737249 | CCCTCTTTGTACCTC[C/T]GGTATAATTCGGCTG | 51429 |
| rs548779627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157867432 | TTCTTCCAAAACAGC[C/T]ACAGCCACTATCATG | 51429 |
| rs548794282 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157944754 | CAGTGTCTGACTCTC[A/G]GATATTTGGATTTGA | 51429 |
| rs548805429 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157779155 | TTGGAGACAATTGCT[A/C/G]TAATTCCTCAAGCTT | 51429 |
| rs548811100 | in-del | -/A | 0.00795532 | 0.062565 | intron-variant | SNX9 | GRCh38.p7 | 6:157938165 | GATTCAGCGCCTCTT[-/A]AAAAAATCAAAGGAA | 51429 |
| rs548835687 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157878479 | CAGTCGCTCAGGCTG[A/G]AGTGCAGTGGCGTGA | 51429 |
| rs548842453 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157938297 | CTAGCCACATGACTT[A/C]CAAAACCTGCTAATG | 51429 |
| rs548845696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157934279 | GAGCATATGGAAATA[C/T]AAGCAATAAAAATTC | 51429 |
| rs548860425 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157756032 | ACAAGATGTTTGCCA[A/G]TAATCACATCTGATG | 51429 |
| rs548861234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157798682 | TATTTCTACAACCTT[C/T]CTCTAAGCTTGAATG | 51429 |
| rs548875041 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157892389 | GCCGTGACGGAAGCT[A/G]CAGGAAAGATCTCCA | 51429 |
| rs548881317 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157725524 | GGCCCTAAGTGAAAA[C/G]AGCTGACCTTGCTTT | 51429 |
| rs548887839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157753015 | ATTAAACCTTGAGTC[A/G]ACACAGCCCATGTTT | 51429 |
| rs548892526 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157806101 | AAATTAATAAAAGTA[C/T]GGTTATATCTTTCAT | 51429 |
| rs548893473 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157844279 | TTATTACTCAAATCA[A/G]TCTACCCATAGAGTT | 51429 |
| rs548905072 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157807699 | GTAAAGGCAGGAGGT[A/G]TCATCCTGGGCCCAC | 51429 |
| rs548907360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157935185 | CTACCTCTGGGTAAC[C/T]GGAATATTGATAAAG | 51429 |
| rs548908974 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157884469 | AGGTTCAGTATTAGA[C/T]GTGCTTATACCTTCA | 51429 |
| rs548919850 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157733205 | CCTGGTGGGGCCGGG[C/T]GCTGTGGCTCACGCC | 51429 |
| rs548934141 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157794314 | ATTGTGAGGCCTCCC[C/T]AGCCACGTGGAACTG | 51429 |
| rs548939156 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157837348 | ACAGTTTTGTGTGTT[A/G]TTAAAACAGTAATCA | 51429 |
| rs548949303 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157791555 | GAGTATTTTTGAAAA[C/G]CTGTGCCCATCCTCC | 51429 |
| rs548949796 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157748919 | AAAATCACAGTAACA[A/G]TAGCATGGCTCTCCA | 51429 |
| rs548955095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157717054 | ATCTAGCCAGCGTTC[A/G]TCCCTTGGTTTTTTT | 51429 |
| rs548965331 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157853801 | ATGTTTAAAAAAAAA[A/C]AACAACAAAGGTGGT | 51429 |
| rs548979673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157940202 | GGAGCGGGGCAGGGA[C/T]CCCAGCTGCCTGCTA | 51429 |
| rs548981231 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157862877 | TTGTATTAACTTGGA[C/T]TCTCTAGGTTGCAAG | 51429 |
| rs548983182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157734001 | GTAAAAATGGTGATG[A/G]ATAACAATAGAAATG | 51429 |
| rs549000149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894397 | TTATAGGCATGAGCC[A/G]CTGTGCCCGGCCCCT | 51429 |
| rs549023502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157764144 | ATGTTATTCTGGAGC[C/T]AACATAGTCTTCCGT | 51429 |
| rs549029075 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157860392 | GCTTGGGTGACAGAG[C/G]AAGATGCGGTCTCTC | 51429 |
| rs549038066 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157739144 | GCAAAAGAAACTATC[A/T]TCAAAGTGAACAGGC | 51429 |
| rs549038359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157835002 | ATGATACCAAAAAGT[A/G]TAGACATTTTAAATT | 51429 |
| rs549047884 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157881282 | TGTAATTGTTTTGAG[A/G]CACCACAATGGCGAG | 51429 |
| rs549051594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157927491 | CAATAGTGTGATGAA[A/G]CCAAGCGGCATGGAG | 51429 |
| rs549057777 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157765557 | AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 51429 |
| rs549074556 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157900378 | AACAGGTTATCAGAT[A/G]CATGGCTCGCAAATA | 51429 |
| rs549080511 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157860614 | TGTTCTTGTGTGCAC[C/T]GCATATAGAAGCTTT | 51429 |
| rs549092334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157725222 | TGCTTTTAGGATTTC[A/G]TTCTTATCACGGGTT | 51429 |
| rs549126729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157868955 | CTCTTCTGTGTCCTC[C/T]CCCTCGTGACCGTCA | 51429 |
| rs549131584 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157763740 | AAACACCAAGGGGAG[A/G]TAGCATGAAATGTTA | 51429 |
| rs549137941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157861774 | CTATGACAAAGTTAA[C/T]TTATAAATTAGATAC | 51429 |
| rs549144985 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157821130 | ATCCTTCCACCTTAG[A/C]CCTCCACCATTACTT | 51429 |
| rs549162452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888600 | TCAGATTGGTTGTGT[C/T]GAAAGTCTCAGCCAG | 51429 |
| rs549164405 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157880707 | GAAAGAGGGAACTGA[C/T]TGAGATCCATTGTTC | 51429 |
| rs549171087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157856439 | TGTAAGTATTTTCAT[A/G]TATACCTCTAAAGAT | 51429 |
| rs549178830 | in-del | -/GGC | 0.0697052 | 0.173187 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157823045 | GCGCCCGGGGGCGGC[-/GGC]GGCGGCGGCGGCGGT | 51429 |
| rs549239296 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157921749 | AGGAGTTAAAATTAT[A/G]TTGGTTAGTTATTTC | 51429 |
| rs549246757 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157863445 | GTCTAGTAGCCATTC[A/T]TGTCATCTGTAATAC | 51429 |
| rs549261518 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157905549 | CCCCCCCACCCCCTC[C/T]CCATAGCCAAATTTA | 51429 |
| rs549302317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157719483 | TAAGCCAAGGACTTA[A/G]AGACAGCAGCAAACC | 51429 |
| rs549308013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157855846 | AGTTCAAGTGATTCT[C/T]CTGCCTCAGCCTCCC | 51429 |
| rs549315229 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SNX9 | GRCh38.p7 | 6:157770591 | AGGAGATCGAGACCA[C/T]CCTGGCTAACACGGT | 51429 |
| rs549326855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157941919 | ATGCACACTTTTCCC[A/G]TCAGTTGGTGCCATT | 51429 |
| rs549361010 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157750309 | CAGACATGTTGACCA[A/G]AAGACCAGAAATAAA | 51429 |
| rs549362251 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157763874 | CCATCCAGCCTTGCT[C/G]CTTCTCCAAATACTG | 51429 |
| rs549374422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157727188 | GTGTTTTCTCGTGGC[C/T]CAATAACGAGAAGCA | 51429 |
| rs549378895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157865396 | GAATTCTGTCCACTT[C/T]TGCAGCCATGTCAGG | 51429 |
| rs549399310 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157729860 | CTCCCCTTGCCCCCA[C/G]TGACCTATGCTACAA | 51429 |
| rs549416026 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157837723 | CCCATATGCATGAAG[C/G]CATGGGCATGCTGTC | 51429 |
| rs549432608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157814712 | GAAAGAACTTGTATC[C/T]CTATCTTAAGTGATT | 51429 |
| rs549443231 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157750809 | ATAGGCAAAGGACTT[G/T]AATAGACATTTCTCC | 51429 |
| rs549444817 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SNX9 | GRCh38.p7 | 6:157765590 | TCGATCTCCTGACCT[C/T]GTGATCCGCCCGCCT | 51429 |
| rs549446173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157874613 | ACTGCTTCATCAAAC[C/T]ACAGCAGCATACACA | 51429 |
| rs549467436 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157870531 | TCACCTGTGCAAGCA[C/T]GCACACCCCTCAGAC | 51429 |
| rs549468652 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157828249 | AGATAAGTTCTGTGA[C/G]AGTAGAAAGATGAAC | 51429 |
| rs549468741 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157922215 | CTTCATTAAAATCAA[A/G]GAAACGTTGGCTGCC | 51429 |
| rs549482675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157914217 | TGGTATCTCAGCATG[A/G]TTTTGATTTGCATTT | 51429 |
| rs549488050 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157823993 | GGACGCCCCGCGCCC[C/G]TTTGCCTTCGCTGCT | 51429 |
| rs549531038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157730195 | GAATTATATCTTAGT[A/G]TAACTGTTTTTTTTT | 51429 |
| rs549558590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157848333 | TGGCTCTGATGGCTT[C/T]AAGCAGAAAAAACTG | 51429 |
| rs549574484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157902116 | CAAAGTATATACCCT[A/G]CCAAGAGGCAGCTGG | 51429 |
| rs549583801 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157924545 | GATCAGACCTTAAAG[G/T]TGGGGGTGGAAAGAT | 51429 |
| rs549597499 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157799718 | AAGCAAAAGCAAAAG[C/T]CCCTGATAAACCCAT | 51429 |
| rs549601592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889693 | CTTAAGCCTGTTATC[C/T]CTTCAATTAAAAGTC | 51429 |
| rs549603924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157892543 | CATAACTTAGGTGGA[A/G]AGCTAAGATCACATA | 51429 |
| rs549607188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157731769 | AAGGATATCATTCCC[C/T]TCTCAAAGACCCTCT | 51429 |
| rs549608303 | in-del | -/A | 0.425123 | 0.178415 | intron-variant | SNX9 | GRCh38.p7 | 6:157743413 | GCCTGAGGCCTATGC[-/A]AAAAAAAAAAAAACA | 51429 |
| rs549613247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157935752 | GATGTCCGGTGAAAG[C/T]GGGTCGGGGTGTAGA | 51429 |
| rs549649324 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157830732 | TAATTTCAGTAGCCA[C/T]ATGTGGCTAATGGCT | 51429 |
| rs549696544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157898725 | CCATTATTTTTTAAC[A/G]ATTCCTGAACCCTGT | 51429 |
| rs549702045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157858802 | GGCAAGAGAGCTTGT[A/G]CAGGGGGACTCCCCT | 51429 |
| rs549711297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157901512 | ATTTTAAGTTGATTT[C/T]TGTGTGTGGTGTAAG | 51429 |
| rs549737972 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157802632 | TATTATAGGATAGTT[C/G]CTTTTTGTGTTTGTG | 51429 |
| rs549775613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157778945 | GCCGGGAGGGCAGCC[A/G]ATGAGCTGGACAGGT | 51429 |
| rs549804809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157789066 | GGGCGTGGTGGCGGG[C/T]GCCTGTAGTCCCAGC | 51429 |
| rs549812673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157779708 | GACTTCCCGTGAAGA[C/T]TAAATTCAATCCAAT | 51429 |
| rs549820990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157756637 | GCTCCTTGAAGGTGG[A/G]CTTTGAGGACCAGCA | 51429 |
| rs549831935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157904664 | ACAGTGAGCCGAGAT[C/T]GCGCCACTGTACTCC | 51429 |
| rs549864148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893161 | AAGAAAACTGTAGAA[A/G]GAAGGGTTTCTCTTA | 51429 |
| rs549881307 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157924989 | TCCTATCCTAGAGAG[A/C]AGGGAAGAATTTCTG | 51429 |
| rs549911729 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157925852 | GATAATTTATATACA[A/T]CAGAAATTTATTTCT | 51429 |
| rs549932534 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157905121 | TGGAGTCAGAATTCA[A/C]ACCCCATGCCATCCA | 51429 |
| rs549933721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157781662 | GGAGTGGAGTTTATT[C/T]TTGGAAGATGAGATT | 51429 |
| rs549936992 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157916817 | ATATTGCTGGATTAA[A/G]TTTGCTAATAATATC | 51429 |
| rs549944828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157723448 | AAAAATAATGCCTGA[A/G]CCTGCGAGAGCTAAA | 51429 |
| rs549951949 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157912759 | TGTTTAGAGATTTTT[A/G]TTTTTTATGGAAATA | 51429 |
| rs549992032 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157810377 | CTCCACTGTGGGGGT[A/G]GTAAGCTGTCTCTAT | 51429 |
| rs550009995 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157715758 | TTGCCATGGGTTTCA[A/T]CTGAGAGAAAAGCTC | 51429 |
| rs550011255 | snp | C/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886497 | CTTTACACTAGGTGT[C/G]TTATTTTCTCTCTGT | 51429 |
| rs550016586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157938498 | AAATTTAGATGCTTT[C/T]CTCTCTTCTTATTTT | 51429 |
| rs550030793 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | SNX9 | GRCh38.p7 | 6:157811068 | CACCAAAACAAAAAA[A/C]AAAAAACAAAAACTA | 51429 |
| rs550045229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157780693 | GAAATTCAAATTTAA[C/T]TGGACCTTCTTTTCT | 51429 |
| rs550050576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157749955 | TGGAAGACTTGTACA[C/T]TGAAAACTACAAAAC | 51429 |
| rs550077320 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157774021 | TCCCATGAAGAAAGC[A/G]TCTGGACTGAACAGA | 51429 |
| rs550080718 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157730681 | GTCTTGCTTTGTCAC[A/C]CAGGCTGGAGTGCAG | 51429 |
| rs550086720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157768440 | TACTTTTACATAAAT[A/G]TTTTTAGAAGCAGAT | 51429 |
| rs550095432 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157797074 | AAAGGGATAATATTA[A/T]GTACCTTAGAGAATG | 51429 |
| rs550101650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157817667 | GTTTGAGACCAGCCT[C/T]GCCAAAGAGACCAGC | 51429 |
| rs550102954 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157795976 | AACTACGAACAAAAT[C/G]AGTATTTTATTTAAA | 51429 |
| rs550106010 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157799793 | AAGACCCGGCCCCCA[G/T]GATTCAATTACCTCC | 51429 |
| rs550139661 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157839180 | AATGAATTGTCCTTG[-/T]GTATAATTACTGTTA | 51429 |
| rs550169457 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157847507 | AATGCTATATATTCT[A/G]TAGGAGTTTTCTTTC | 51429 |
| rs550196208 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157872370 | GAGGAACCATGGATC[A/G]GTTCACTTTTTCTGC | 51429 |
| rs550200018 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157769993 | TGCTTGAGTAAATGT[G/T]GTCACCATCTTGAAA | 51429 |
| rs550214668 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157744494 | AGCCATGAGCAGAAA[G/T]CACATTCATTTTCTC | 51429 |
| rs550217820 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157913329 | TTTATTTATTTATTT[C/T]TGGAGACGGTCTCAC | 51429 |
| rs550261670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157760166 | GTGAGCCACCACGCC[C/T]GGGCCATCAAGGTTA | 51429 |
| rs550270152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157896311 | TCAAATTAAAAAGCC[C/T]ACTTAAAAATACAAC | 51429 |
| rs550279444 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157938973 | TGATTAAAACTGTAC[A/G]TTTTATTATTTCTGA | 51429 |
| rs550285430 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157753914 | GAGCAGAGTTTTTAA[A/G]GATAATTTGGTGGGT | 51429 |
| rs550291198 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157777982 | TCAGATTTTTTTTGT[A/G]TTGATTTCCTATTAC | 51429 |
| rs550315693 | in-del | -/CTC | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157733706 | ATGCCCTCCCCAGAT[-/CTC]CTCAGCAAGCTTGAG | 51429 |
| rs550338514 | snp | A/T | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157932926 | GCCATTTCAAGGAAA[A/T]ATGTTTGACCAAGTA | 51429 |
| rs550384267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157819225 | TCTTCAGAGCACTTA[C/T]AAAAGCACCTGGCAC | 51429 |
| rs550391517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157738390 | CCCTTTACCTATGTA[A/G]TGCCCTTCTTTGTCT | 51429 |
| rs550412591 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157805481 | GCCAATTACCTGCCT[C/T]CATGTGGGCTCCCAG | 51429 |
| rs550415987 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157867106 | GGTGCTGGCTACAAT[A/G]CCCAGCTAATTTTTC | 51429 |
| rs550430337 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157928323 | AATTTTCCTAAATAA[G/T]ATATTCAAGAAATTA | 51429 |
| rs550452896 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157873782 | CCTTCTCCCATTCCC[A/G]TAGACAGAGGGGTGT | 51429 |
| rs550470089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157832585 | TTTAAATGACTCACA[A/G]TTCCAAAGGGCTGGA | 51429 |
| rs550502825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157737841 | GTGTCCCAGAGATTC[C/T]CATACGTTGTGTCTT | 51429 |
| rs550514431 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157777337 | GTGAGCAGAGATCAC[A/G]CCACTGCACTCTGGC | 51429 |
| rs550515047 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157908612 | TGTACATGAGCTCCA[C/G]CATCCAGGTTCCTCT | 51429 |
| rs550515915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157875319 | TTCTGTGGCATTTCT[A/G]TTGGGTACTAACAAA | 51429 |
| rs550554907 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157807449 | TAGCTAATGCAGACC[C/G]TACTCTCTCTTTATC | 51429 |
| rs550560307 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157929053 | ATCTTCATCCATTTG[G/T]TAAGATGTTGTGTAT | 51429 |
| rs550569934 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157929407 | AGTGACTTGTCAGGC[C/G]CTGAAATGCTGCGAC | 51429 |
| rs550579019 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157882449 | AGTAATTTTGACTTC[C/T]AAGTCCTATAAGAAA | 51429 |
| rs550594345 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157883085 | ACCTTCAGCAACCAC[C/T]ACCCTGATCAGTCAG | 51429 |
| rs550595666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157850010 | AGAGTGTAGGACCCT[A/G]GAAAACACAGACATT | 51429 |
| rs550603610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157759508 | GAGGTCAGCATGGCC[A/G]ATATGGTGAAACCCT | 51429 |
| rs550604836 | snp | A/T | 1.87908e-05 | 0.00306514 | intron-variant | SNX9 | GRCh38.p7 | 6:157936077 | TCCAATTAAGATTTG[A/T]TGCTATCTAGTCCAC | 51429 |
| rs550622503 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157908950 | AGGTGGACGTGATAC[A/C]CGGGGGTTGGAAGTG | 51429 |
| rs550622545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157916137 | CCTCCTGGGTTCACA[C/T]CATTTTCGTGCCTCA | 51429 |
| rs550637195 | in-del | -/ATGGA | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157803709 | TATCGAAGAGTCTGT[-/ATGGA]AAAGTGTTTAAATTA | 51429 |
| rs550665474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157815646 | TAGGCTCTCAATAGA[C/T]AGCTTAGGCGTGAAA | 51429 |
| rs550666109 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157798975 | ATTATGAACAAAAGA[A/G]GTTTAATTGACTCAC | 51429 |
| rs550678930 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157935288 | AAACTCATACTAAAA[G/T]AAAAGATCCAGACAA | 51429 |
| rs550678944 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157941482 | TCACAAAACAATAAC[A/G]AAAACTTAAATTTTT | 51429 |
| rs550708739 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157734435 | TTTACAAAGACAAAG[G/T]TCTTCTTGTCCTCCT | 51429 |
| rs550720995 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157797908 | TAAATAAGCGTGGGG[-/A]AAAGAAAGCTTTTCT | 51429 |
| rs550723259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157776890 | AATCCTTCACTTCTC[C/T]GAGGAATCCACTCTT | 51429 |
| rs550727480 | in-del | -/T | 0.237812 | 0.249703 | intron-variant | SNX9 | GRCh38.p7 | 6:157938785 | AGGTGCTGGTGGAAG[-/T]TTTTTTTTCCCCAGC | 51429 |
| rs550734429 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157834507 | GTGTGCCACCCCCCC[A/G]GCCAATTTTTTAAAT | 51429 |
| rs550739363 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157730480 | GCAGTGAGCTGAGAT[C/T]GTGCCACTGCACTCC | 51429 |
| rs550742763 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157923802 | ACAAAGATGGCACTG[A/G]GCGTAGTAGGCAAAG | 51429 |
| rs550746338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157897621 | CAAGTGATTCTCTCA[C/T]CTCAGCCTCCTGAGT | 51429 |
| rs550760941 | snp | A/C | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822068 | CAATATTTTTTTTTA[A/C]GGAGAAAGACAACTA | 51429 |
| rs550769564 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157925618 | AAGTAGAATATTATA[C/T]AGCAATGAAATGAAT | 51429 |
| rs550773857 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157843660 | TAAAATGTATAATGT[G/T]CATTTACTCACCAAT | 51429 |
| rs550793611 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157772009 | CGGCCCGGCAGCCAA[A/G]TTTTAAGAACCAGGA | 51429 |
| rs550815557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157734793 | GTTTTCAAGGGGGGT[A/G]TTTCAACTAAGAACC | 51429 |
| rs550823477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157921941 | GCAGTTTTTCCCTAG[A/G]TGTTTTTAAAAATAG | 51429 |
| rs550828573 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157728523 | TAAATTTATGATGTT[A/C]TCTGTTCTCCGCAAC | 51429 |
| rs550830984 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157944701 | TCCGGGAAGCGTATC[A/G]TAACCACCTGGGAGT | 51429 |
| rs550856237 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157747231 | GAAAGTAATGCCCCC[A/C]CACAAACCAGAACAG | 51429 |
| rs550862057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157746643 | GAGGGGGAGCCTGGC[C/T]GGAAAGAGAGGAAGG | 51429 |
| rs550877432 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157748109 | TCTGTTAAATACAAA[A/G]CAACATCATCCATCA | 51429 |
| rs550888033 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157843052 | AGGTTACAAGCAAGA[A/T]AGAGTTGGTTAGGTC | 51429 |
| rs550918951 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157944107 | GCACACCGTCAGCTC[A/G]AACTCAACACTGGCA | 51429 |
| rs550933706 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157836283 | TCTGGAGTTTTCATT[A/T]TGAAAGTGATAGATA | 51429 |
| rs550948457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157729480 | CCTTCCCTGCTTTGC[C/T]TTTATAGTTTTAAGT | 51429 |
| rs550956970 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157849810 | TGTGCTGGAATGCTG[A/T]TGAGGCCTTGCTTGG | 51429 |
| rs550962917 | in-del | -/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822439 | TATATCTCCAACTCT[-/G]GGAAAGAAACACTGA | 51429 |
| rs550974043 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157716520 | TTCCTGTGGCACTGG[A/G]AGGCGAGCCGTTGTC | 51429 |
| rs550982311 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157944716 | ATAACCACCTGGGAG[C/T]TGCCAAGAAGCAGAC | 51429 |
| rs551015472 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157760181 | CGGGCCATCAAGGTT[A/T]TTTACATCTGCGTGT | 51429 |
| rs551049288 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157934670 | AGGATAAAGCAAATA[C/T]GTAATTATGTTACTG | 51429 |
| rs551072394 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157864211 | GTTGTGTCCTGACAC[A/G]GCAGACGGGTGAGCG | 51429 |
| rs551074379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157869937 | ACCTCTCATGCTCTC[A/G]TACACTTTACATACT | 51429 |
| rs551075362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157902417 | TGTTAATCACTTGCC[A/G]TGTGCCAGGCATTGT | 51429 |
| rs551079116 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157831291 | TACCTAGATTGAGGT[G/T]GTATCCTTCCAGGGA | 51429 |
| rs551079567 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157811458 | TTATTCAATATATTA[A/T]AGTTGCTTAAAAAAT | 51429 |
| rs551089398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157772440 | AAAGAAAATGGGGGC[C/T]AAACACAGGGATGAA | 51429 |
| rs551093720 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157856741 | GATTTCTTACCTTAC[C/G]CTCATTACATAGTTT | 51429 |
| rs551114474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157852393 | CCATGGTTCTCAGAA[C/T]TCACAATCCTCCTTT | 51429 |
| rs551134174 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157755956 | ACTCCTGGCTTACTG[G/T]CTTTCCCCCACCCAC | 51429 |
| rs551145381 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157912071 | CAGTTCAGACACTCC[C/T]TGTACCTCAACCCGG | 51429 |
| rs551151092 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157835212 | GAGATGGGGTTTCAC[A/C]ATATTGGCCAGCCCA | 51429 |
| rs551162376 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157891345 | AAAATCATTTTTTCT[A/G]TAGTCACATGCTGAA | 51429 |
| rs551169972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157732229 | CCACTAAGAATGCAG[A/G]ACATCACAGAGCCAT | 51429 |
| rs551170423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157846608 | AGTATTTAAATTCTT[C/T]AAAAAGGCCCAGAGA | 51429 |
| rs551194870 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157794380 | CCTGTCTCAGGTATG[C/T]CTTTATTAGCAGCAT | 51429 |
| rs551196858 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157902870 | ACGAGGTTTTACCAC[A/G]TTGGCCAGGCTGGTC | 51429 |
| rs551226228 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157884157 | AATCAAAAATGGGAA[G/T]ATTCTCTTACAGAAA | 51429 |
| rs551239285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157804790 | CCAAGTTGACACATA[A/G]CATAATCACCCCAGC | 51429 |
| rs551246196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157939560 | TGAGGGCCTAAAGAT[A/G]TGGTACTGGGGAGAA | 51429 |
| rs551254946 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157760786 | CCTGGGTGGGGACAG[A/G]GAGTTGCACAGACTG | 51429 |
| rs551255469 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886916 | GGAAGCCCATTCAAG[C/T]TGAGTCTTCTACCTC | 51429 |
| rs551294329 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157926719 | CTGGAAGCTCAAGGA[A/T]ACAGTGAGCTGAGAT | 51429 |
| rs551306068 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157790957 | TTAAAATCCTGTGGT[C/G]TGGCTCCTAACTGTT | 51429 |
| rs551309817 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157846048 | TGGTGAGAGGCGCCC[A/G]TCCTGCTGTGCAGGT | 51429 |
| rs551311930 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157751346 | TCCCTCCCACAACAC[A/G]TGGGAATTACAGGAG | 51429 |
| rs551314960 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157880126 | CCAGGTGAGTGGTGT[C/G]GTGGGAAGCATGTAA | 51429 |
| rs551337923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157905949 | AGATCAAGCTTAATT[A/G]AATGCCTAATTGGCC | 51429 |
| rs551352750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157739141 | ACAGCAAAAGAAACT[A/G]TCATCAAAGTGAACA | 51429 |
| rs551357253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157867053 | TCCTGGGCTCAAGCA[A/G]TCCTCCCGCCTCAGT | 51429 |
| rs551379550 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157899298 | TTAGTGTTAAACAGC[C/T]GCTTTTCAAAGTTCT | 51429 |
| rs551380738 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157860539 | TAATCGTGATGGTAC[A/G]TGTGATATGGCCAGT | 51429 |
| rs551409407 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157881484 | CTCTCACTTTAAATC[A/G]AGAGCTAGAAATTAT | 51429 |
| rs551410557 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157762972 | GGCAAATAGAGCGAG[A/G]GCAGAGAGCTCTCCT | 51429 |
| rs551411705 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157792472 | TGACAAAAATATATA[A/T]CTTTATCATGTACAC | 51429 |
| rs551414070 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157840390 | ACACCCAAAATGACT[A/G]ACTTTTACAAAAAAT | 51429 |
| rs551428167 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157744685 | CTGGAACCAACAGGG[A/C]TGATGACAGCATTTT | 51429 |
| rs551431109 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157933535 | CTGGCCTTACCATGT[C/G]TTACAGTTGACACTT | 51429 |
| rs551440919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157899824 | TGATGTTGTAATATA[C/T]ATGTATATACTGAAA | 51429 |
| rs551443045 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157861291 | AAACTTCATTTCCTT[C/G]TTTGGAAATTTTAAG | 51429 |
| rs551446039 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157745477 | AACCTAATAAACTCC[C/T]CTGCAGGCATGGAAC | 51429 |
| rs551456076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157881426 | CCAATTATTAACCCT[A/G]CAGTGGCCTCTAAGT | 51429 |
| rs551464980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157834878 | GTAAAGCGTATTCAA[C/T]GTCCTTGCAACCCCT | 51429 |
| rs551465826 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157745097 | TAAGCAAAGGAAGAA[G/T]GGTAGATAGGAAAAG | 51429 |
| rs551470645 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157939969 | GTTGGGGGCAGGGGC[-/A]GGGGGGACAGAGAAA | 51429 |
| rs551480716 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157724644 | CCTGAAAGAAAAAAA[-/C]ACCTTGACTAATCAG | 51429 |
| rs551503305 | in-del | -/ATA | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157837385 | ATTTATTTGCATTGT[-/ATA]ATATGTTCCTACCGT | 51429 |
| rs551518937 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157874515 | CCTCTATTAGAAATA[C/G]ATCCTGCAGGCAGAA | 51429 |
| rs551534187 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157752019 | AACACGGTGAAACCT[C/T]GTCTCTACTAAAAAC | 51429 |
| rs551537647 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157833363 | CTTATATACCTTCTG[A/T]TAATTTGTTTCAAAT | 51429 |
| rs551551596 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157752430 | CAGACAGGGGGATGT[C/G]GCAGGACAATAGGGT | 51429 |
| rs551552684 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157797398 | GTAATAATATAAAGC[A/C]TATGCTTTGACATAT | 51429 |
| rs551560089 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157934123 | CAATAATGTAAATGG[A/G]TTTGATTCCTGGAAA | 51429 |
| rs551583375 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157794790 | CTAGATGTTTTAAAT[G/T]ACTTACTTTTAAAAA | 51429 |
| rs551586751 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157842536 | GTTAGTCAGTCTCCC[C/T]GAGCATTTGGGGATT | 51429 |
| rs551607854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157882644 | AGAAGTAGATTCCAA[C/T]CCTCATAGAAGATGT | 51429 |
| rs551632431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887800 | GAGAATAATACCACC[A/G]CTTATTTCACAGGAG | 51429 |
| rs551640760 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157798148 | AACCTAGAAGACAAC[A/T]CTCTAATCAAGTGAT | 51429 |
| rs551655535 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157868127 | AAATCAGATTAGGTT[G/T]CCAGAAAGCAATATA | 51429 |
| rs551664486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157908086 | CGCTTTTCCCATCTT[C/T]CTCTTAAAAAAAAAA | 51429 |
| rs551669856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157804138 | TGCTCATATTACAGG[C/T]GTGATCCACCACGCC | 51429 |
| rs551727487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157782841 | CAGTGAGCCAAGATC[A/G]CGGCACTGCAGTCCA | 51429 |
| rs551729031 | in-del | -/TTGG | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157804451 | GCTGGTTTCAAGGAC[-/TTGG]TGAGTGTATCTGTAT | 51429 |
| rs551729476 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157818838 | CAAACGGTTCCTGTT[-/C]CAGCCTAACACCGCC | 51429 |
| rs551733616 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157907583 | GCCACTGCGCCCGGC[C/T]TGCCTCACATTCTTA | 51429 |
| rs551734379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157901432 | GCCAGCGCCAAGGAG[C/T]TTTTCCCCTGTGTTT | 51429 |
| rs551743702 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | SNX9 | GRCh38.p7 | 6:157741368 | CAACAACAACAACAA[A/C]AAAAAAAAAACAGAG | 51429 |
| rs551748498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157906776 | CTTCGGTTTCATTCC[A/G]CATTTTGATTGGTGG | 51429 |
| rs551757892 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157934402 | TACATAATTATTAGA[A/G]AACAAATTTAAATCA | 51429 |
| rs551764314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157775052 | GCTGATCAACACAAA[C/T]GCCATGCAAAGACTT | 51429 |
| rs551786614 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157877731 | TGGGCCTCTCTCCTG[A/T]CCATCAGGCCCATGG | 51429 |
| rs551788380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157870097 | CACTTGCCCTCATCC[A/G]CACTCATGCTGTCAC | 51429 |
| rs551788960 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157901136 | CTCTCTGCAGGGGGA[A/G]GCACATCACATGCTG | 51429 |
| rs551813787 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157732109 | GGTAGGAAGGAATTT[G/T]TGTGGGAGAGCCTGG | 51429 |
| rs551848555 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157871373 | GAGACAAAATGAGAC[-/A]GTGTCTCAAAAAAAA | 51429 |
| rs551850811 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157799931 | ATGAGATAAAGAATT[A/G]TCCCAAGTCTCCATG | 51429 |
| rs551855934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157748023 | GACAGAGTTGAGATT[C/T]GAACCCAAGCAGTCT | 51429 |
| rs551863170 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157796182 | TGCTTCCTTCAATAT[A/G]AATATGCTCGCAATG | 51429 |
| rs551880651 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157790551 | CAACCCCACTCCCCC[A/C]ACCCCCAGCCCTGTT | 51429 |
| rs551888904 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157778121 | CCATGTTCTCTCAGG[A/G]GGCGCTACGGGAGGG | 51429 |
| rs551909548 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157735681 | CCACCAAAATCCCAC[C/G]TGAGGGCCTGGCGCA | 51429 |
| rs551934748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157900777 | TTAAAACAGAAACAC[A/G]GTCTTTCCATAACCT | 51429 |
| rs551941795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157920186 | TTCTACCAGACCCTT[C/T]TGTGTCTCCTTTACT | 51429 |
| rs551955630 | in-del | -/CAGGCGGATCCC | 0.0019976 | 0.0315406 | intron-variant | SNX9 | GRCh38.p7 | 6:157756759 | ACGCAGGCGGATCCC[-/CAGGCGGATCCC]CAGGCGGATCCCCAG | 51429 |
| rs551958589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157930358 | AATAATGTATACAAA[C/T]GCAGCATCTAGAAAA | 51429 |
| rs551965846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157767827 | AAGTATGGCTTGGGT[C/T]CCCAATGTCAGGCCA | 51429 |
| rs551976883 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157930874 | GCAAGACCATCATAA[C/G]ACATCATTTAAATCT | 51429 |
| rs551991076 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157813888 | GGAAATTGCTATTAT[A/C]TCTCTCTCTCTCTCC | 51429 |
| rs551994385 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157916014 | TTTTGTGGGTATGGA[C/T]TCTTTGGTTTTTTTG | 51429 |
| rs551995438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157883547 | ATTCATCTGAATTTG[A/G]GGTTGAAGTACTTTT | 51429 |
| rs552029619 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157814549 | CCTATACAGTTCACA[A/G]GGCCTCAAGAATAAA | 51429 |
| rs552047549 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157870463 | GCAGCACTCACCCGT[C/G]CAAGCACATACACCC | 51429 |
| rs552049014 | in-del | -/CTT | 0.00119737 | 0.0244387 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886006 | TTAAACCTAGCCCTC[-/CTT]CGAGGCCTGATGTAG | 51429 |
| rs552066463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157820065 | AAAGGCAGGCCTGCG[C/T]AGAGAATCAACTCTA | 51429 |
| rs552079654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157767416 | GCACCTACCTCATGG[A/G]GTCATTAGAAAGACT | 51429 |
| rs552084437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157725905 | GATTCTTCCCGAACA[C/T]CAAACAAGAACCTGA | 51429 |
| rs552104304 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157794577 | CTAAAAACGAACACA[C/G]AACATCTTTATATTT | 51429 |
| rs552125748 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157865425 | GGAAAACACCTCAGC[A/C]TGGCTGCTTTGTTCT | 51429 |
| rs552134910 | snp | A/C | 0.0225045 | 0.103662 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157892487 | CAGGAAAAAAAAAAA[A/C]AAAACCAAAGAGATA | 51429 |
| rs552141695 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157726367 | GTCTCTCCTTAACTA[C/T]TTGAACATACAGAAT | 51429 |
| rs552199079 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157916264 | TGGTCTCGATCTCCT[C/G]ACCTCATGATTCACC | 51429 |
| rs552199559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157924302 | ATACCTATGAAACAA[A/G]ATTGGCACCTCCCGG | 51429 |
| rs552203080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157836518 | TCACAGTCACCAACC[C/T]GGGGAGCTTGTTAAA | 51429 |
| rs552204346 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157768405 | ACCCTGGGTTTAGCG[C/T]GATGGCTGTTTTGTC | 51429 |
| rs552209830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157910539 | TTATTTTGATTATTA[C/T]CCTCTCCCTTTTCTT | 51429 |
| rs552213098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157755180 | TGACCTGCATCTTGT[A/G]CTGACCTCTTATCTC | 51429 |
| rs552251761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157740950 | AGGGAATGACATCTA[C/T]TTCATAAATTGCTAT | 51429 |
| rs552259611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157891583 | CATTTAAAATATTTG[A/G]GTCCTTGCCACTTTA | 51429 |
| rs552271868 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157898617 | GGCTATGAATAGAAA[C/T]ACTGAGGCAGAAGAG | 51429 |
| rs552333206 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SNX9 | GRCh38.p7 | 6:157824982 | GGCGCGGTGGCTCAC[C/T]CCCACCTGTAATTCC | 51429 |
| rs552340730 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157871694 | ATAATTTTTAAAAAT[G/T]TTTAAAAATGCTAGA | 51429 |
| rs552352139 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157780698 | TCAAATTTAACTGGA[C/T]CTTCTTTTCTGTTTC | 51429 |
| rs552355723 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157779489 | CATTTTAAAAGACAA[A/T]TAATGTAATTAGATT | 51429 |
| rs552393500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157904586 | CCCACAGAAGCGCAC[C/T]TGTAGTCCCAGCTAC | 51429 |
| rs552395041 | snp | A/C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840914 | TTATGCTGTTCACTC[A/C/G]ACTGGTGGCCACATA | 51429 |
| rs552407772 | snp | C/T | 1.64751e-05 | 0.00287007 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157910000 | AGCCATTCCAATCCC[C/T]TCTCTTCCAGACAAA | 51429 |
| rs552427363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157925230 | ATAAGGTATCTGAAT[C/T]AACAACAGATGTGTA | 51429 |
| rs552438534 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157813931 | AGGTCAGATAAACAA[C/T]GTAGTTTTGGCTTGG | 51429 |
| rs552438917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157938405 | CTCTTTTGTTGTAGC[A/G]TAAAACTGTTCATTT | 51429 |
| rs552441466 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157919882 | AGGTTGTTGTTTCTG[A/C]TTTTTATTTGTTAAG | 51429 |
| rs552445127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157864801 | TTGGGAGGCCGAGGC[A/G]GGCAGATCATGAGGT | 51429 |
| rs552457984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157780113 | AGGACCCCAAGGTCC[C/T]GCCTGGCTCTCCTGC | 51429 |
| rs552467385 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157823168 | CGTCGCGCGCGCCGC[A/G]GTAAATGGGAGGCTC | 51429 |
| rs552482952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157917870 | GTTGAATCCATGGGT[A/G]CAGAGACCGTGGATA | 51429 |
| rs552487245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157925664 | ACAAGATTTTGACTG[C/T]AGTTCCTAAGCAAGA | 51429 |
| rs552500178 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157776789 | ATGAAGGATGGTGGA[A/G/T]TTACTGCGAAAGCAA | 51429 |
| rs552504420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157823864 | CCCCTCCCGCTGCCG[C/T]CTGGGGGACCCTCGC | 51429 |
| rs552505767 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157802598 | TTTTAACCTTGGGTT[A/C]CAAGAAACTTTCCTG | 51429 |
| rs552508208 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157717039 | TGTGACACCTGATCC[A/C]TCTAGCCAGCGTTCG | 51429 |
| rs552512659 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157778391 | GGCAAAATTCAACCC[A/C]CAGCACTTCCTAATG | 51429 |
| rs552519355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157730883 | GCCTCATGTGATCTG[C/T]TGGCCTCAGCCTCCC | 51429 |
| rs552520149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157756517 | CTTTATAAATTTGCA[A/G]TCTGGTGTGCCATGT | 51429 |
| rs552524803 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157784831 | TCAAAAACTTTCCTA[C/T]GCTGTTTCTCTGGCA | 51429 |
| rs552542513 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157729635 | AATAAAACAAAGTTG[A/C]ATTCCTCACTTACTT | 51429 |
| rs552556578 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157919711 | CAAATTCAACATCTG[C/T]GGACACTCAGAGATA | 51429 |
| rs552560391 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157927749 | TTTTTTTTTTTGAGA[C/T]GGAGTCTTGCTCTGT | 51429 |
| rs552583778 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157748990 | CATTATCTCAATTAC[C/T]TTCTTACATCCTGAG | 51429 |
| rs552593142 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157851582 | CTCACATAGTGGAAT[C/T]ATATATTCGTTGTTT | 51429 |
| rs552603201 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157878692 | CACTTCAGCCTCCCA[A/G]TTGCATCCGGCCTAT | 51429 |
| rs552613245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157844367 | GGGGTGAAATCACAG[A/G]GAGTCAAAGCTGTCT | 51429 |
| rs552623775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157858759 | TGGAAGGCAAAGGAG[A/G]AGCAAAGGGACATCT | 51429 |
| rs552629544 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157850955 | ACTTATTTCTATGGT[A/C]TTTTGAAAATAGTGA | 51429 |
| rs552654474 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157873898 | TGCCTGGGACACCCC[C/G]AAGCTGAGCCAACCA | 51429 |
| rs552667067 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157737818 | TCCCTCTAAACACTG[A/C]TTTAGCTGTGTCCCA | 51429 |
| rs552676775 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157723367 | AAAAATCTTTTCTTA[A/G]TAGTCAAAGTTTCCT | 51429 |
| rs552688892 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157943402 | CTTACACTTCAAGAG[A/G]GAGGACGCTGGGGGC | 51429 |
| rs552690718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157850761 | CCTGAAGGCTCCTGG[C/T]AGGTCACTTTTAAGA | 51429 |
| rs552709769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157879063 | CAATGTCATACAAAG[C/T]GAGGGAAAGGATAAA | 51429 |
| rs552710944 | snp | C/T | 0.031825 | 0.122064 | intron-variant | SNX9 | GRCh38.p7 | 6:157840446 | TTCTTTCCTTTCTTT[C/T]CTTTCCTTCCTTCCT | 51429 |
| rs552727244 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157899149 | GCCCACAGCACCTTA[C/T]CTGACACGGGGATTA | 51429 |
| rs552739060 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157780573 | TCTCTGTTAAATTTG[A/T]ATTTAAGATAAACAA | 51429 |
| rs552773210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157726151 | GTCCCATCTCACCAC[A/G]CTCAGTGATGGACCA | 51429 |
| rs552776622 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157871317 | GCCCAGGAGTTCCAG[C/G]CTGCAGTGAGCCAAG | 51429 |
| rs552795082 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157743801 | TGGTGGATCACTTGA[A/G]GTTAGGAATTCAAGA | 51429 |
| rs552804084 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157853495 | ATAGTTTTCACAAAT[A/T]GGAAATTTTTGACAT | 51429 |
| rs552804091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157827189 | AACATATATTATAGT[C/T]TATATAATATATAAA | 51429 |
| rs552818383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157920446 | AAGCTGCAGCTGCCC[A/G]TCTTCACAGCCTGTC | 51429 |
| rs552835682 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157798097 | AAGTACCTCCTTACC[-/AG]AGTCTTACTAGCATC | 51429 |
| rs552839635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157934529 | AAATGGCATTTTATA[C/T]GCCCCCAGGAGCGGG | 51429 |
| rs552868535 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157749812 | CCACCACACCCAGCC[A/C]CTAACTCCTGCTAAG | 51429 |
| rs552888687 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157914324 | TTCAGCTCTTGTGCT[A/C]ATTTTTTATCAGTCT | 51429 |
| rs552890286 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157827882 | TTTTTTTTTTTAACT[C/G]TTCGGTTCCAATACC | 51429 |
| rs552893425 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157852406 | AATTCACAATCCTCC[C/T]TTCCATTTTTTCCTC | 51429 |
| rs552895245 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157825913 | TAGTAATGACTAACT[A/T]TTAATAAAAATGTAG | 51429 |
| rs552905477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157750847 | ACATGCAAATGGCCA[A/G]CGGGCATATGGAAAG | 51429 |
| rs552905780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157742697 | ATGGTCTTTTGGGCC[A/G]ATGGCATTTCTCCTG | 51429 |
| rs552910083 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157875429 | TAGAAGTCTGTCATG[A/T]TATGAACACAGACCC | 51429 |
| rs552929418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157868420 | TGCCCTCCCAGAGAA[A/G]CATCTATGTGATCTC | 51429 |
| rs552947869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157834492 | GCTTGGACTACAGCT[A/G]TGTGCCACCCCCCCG | 51429 |
| rs552951566 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157900751 | ATGCATCAGTAATTT[C/T]TGACAGAGCCTTAAA | 51429 |
| rs552971434 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157782442 | TCTACTGCTATAAGG[G/T]TCTTATGAAGCATAT | 51429 |
| rs552971973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157941612 | GTAGAATCCAGCCTC[C/T]GCTGGCGGCCTTGCT | 51429 |
| rs552981399 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157744802 | CAGGCTGGAATGCAG[C/T]GGCATGATCTCTGCT | 51429 |
| rs552989196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157880371 | TTTGTGTTCCAGCCT[C/T]TCTCACTATTCTACC | 51429 |
| rs552989960 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894160 | TGTCGCCCAGTCTGG[A/T]GTGCAGTGGCGTGAT | 51429 |
| rs552993139 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157739207 | TATGCATCTAACAAA[A/G]GGCTAATATCCAGAA | 51429 |
| rs553015071 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157820763 | CCCACTGCAACCTCC[A/G]CCTTCCGGGTTCAAG | 51429 |
| rs553050518 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157873653 | AGATATATATTTATA[A/G]TATGACACATATAAC | 51429 |
| rs553051356 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887302 | ATCATGAAGTTTTCC[A/T]TCTAGGCTGGTGGGA | 51429 |
| rs553087382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157846111 | CGGCTTCTCTGCCTT[C/T]GCATCTGATGCATCC | 51429 |
| rs553088277 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157727320 | TGCTTATATAGATTG[G/T]GGTCATATGCCTATG | 51429 |
| rs553106377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157867796 | ACATGATTTTTTTCC[C/T]GTTGCTTATGAAATA | 51429 |
| rs553111397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157759585 | CTGTAGTCCCAGCTA[C/T]TCAAGAGGCTGAGGT | 51429 |
| rs553131736 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157788425 | TTGTCTAGAAAGATT[C/G]CCATATTTCATTATT | 51429 |
| rs553142523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157752140 | AGGTTGCAGTGAGCC[A/G]AGATTGCGTTACTGC | 51429 |
| rs553150358 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157907664 | AGCCTTTCATTGACC[A/G]GCAAGTTTTAAGTAG | 51429 |
| rs553157442 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157942013 | TGCAAGGGCAACTCT[-/C]CAAAATTTTGATAGT | 51429 |
| rs553169115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157775462 | TCAGAGAAAGAAACC[A/G]GATCTTTCTCCTCCA | 51429 |
| rs553181096 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157808571 | ATTCACCCTTTTTGC[A/C]AGCTCTGTGAAAATG | 51429 |
| rs553196405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157738734 | CAAAACAGCATGGTA[C/T]TTGTGCCAAAACAGA | 51429 |
| rs553196693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157875508 | GAAGAGGAGGCTCTT[A/G]TTGTTGAGGAGGTCA | 51429 |
| rs553206882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157753567 | GTTAAGTCCAGAGAA[A/G]AACAAGGATCTGTGT | 51429 |
| rs553250892 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157754666 | GCCTCTGAGTTTCGA[A/G]AGCAAAATTTCTGAG | 51429 |
| rs553265012 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157725101 | TTTTTTTCCCGATAC[G/T]TCAGATGTTGCTCCA | 51429 |
| rs553267360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157745541 | CCCCTCTGTAATTTG[C/T]GGAGCCAAGAAAAGA | 51429 |
| rs553280116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157732527 | AGTTAATTAACACAT[C/T]CCTCGCTTCCTACCG | 51429 |
| rs553290455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157941205 | GGGGTCTTGGATGCT[A/G]GTTGCAAGGCCCCAA | 51429 |
| rs553299586 | in-del | -/TTAGGCCTTTCCTCC | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157839777 | CCTCCAGTCTCCTCT[-/TTAGGCCTTTCCTCC]TTAGGCCTTTCCTCC | 51429 |
| rs553307702 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157835886 | GTGTGAAAACAGACT[A/C]ATACAGTCTGGGACC | 51429 |
| rs553374280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889069 | CTGAGTGAAGGAGCC[A/G]AGGGGATTATTGCAT | 51429 |
| rs553383521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157895664 | AATAATACAATTTAG[A/G]CCAACTTAGTGTTTA | 51429 |
| rs553406260 | in-del | -/AA | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157898325 | CTGGGTTGGTAAAGT[-/AA]AAGCAGAATGGGCGG | 51429 |
| rs553410210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889731 | ATATGACCTGGCTGT[A/G]CAGCTATTTGTAAAT | 51429 |
| rs553411164 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157767398 | AGAGCCAGGATGATG[A/G]CAGCACCTACCTCAT | 51429 |
| rs553423222 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157785793 | ATACACTTTGTACAC[C/T]TGCTACTAAAGAGAA | 51429 |
| rs553435453 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157805215 | CTAGGAGCTGGCCTT[A/C]ATCCTGACCCTCCCT | 51429 |
| rs553444356 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157857959 | GTGGTTCTTGTGGTC[A/T]GGAGAGCCCATCTGA | 51429 |
| rs553451094 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157942925 | TTCCCCTATTATTCA[C/G]AAAAAAAAGGAAACA | 51429 |
| rs553462046 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157759038 | AAAACACCAACAGCT[C/G]AAGGGCCAGCAGAGG | 51429 |
| rs553491822 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157770934 | CAATTTGTGAATATA[C/G]CTATGCTTATATTTA | 51429 |
| rs553510860 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157856612 | AGTCTGCATATTACT[A/C]TCACGATCAATCTTC | 51429 |
| rs553510907 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | SNX9 | GRCh38.p7 | 6:157740002 | ATACCTAATGTAAGT[G/T]ACAGGTTGATGGGTG | 51429 |
| rs553557499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157816750 | TGGCCACCACCACCA[C/T]GAAGCCCAGCACATC | 51429 |
| rs553595463 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157878850 | TCCATTCATATACAT[A/C]CACTCTTGCTAATCT | 51429 |
| rs553626252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157721638 | CCTCTTCCCCACCGC[A/G]GCTCTCTCCTCTGAC | 51429 |
| rs553638384 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157732261 | CTCACAGCACTCCAC[A/G]CCTTCTAACATTCTG | 51429 |
| rs553679969 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157722801 | TGAGGTCAGGAATTC[A/G]AGACCAGCCTGACCA | 51429 |
| rs553714529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157773593 | TAACATGTGAAAAGC[A/G]AAACTGAAAGGGGCA | 51429 |
| rs553727377 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157809873 | AATTGGGAATGGAAA[A/G]TGGTACTGCCATTTT | 51429 |
| rs553737954 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157745644 | TCTGCCCAGGGTGAT[A/T]TTTCACCTTAAATTT | 51429 |
| rs553740759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157891883 | TGAAGTTTGAAGCTT[C/T]AGAGTGAAGGTTAGT | 51429 |
| rs553755194 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157774082 | GGGCAGAGGAGCCTG[C/T]CCAGGGGACCGCAAA | 51429 |
| rs553765039 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157844033 | GCCCATACCTCCTCA[A/C]CTGCCTAATTTTTGT | 51429 |
| rs553786261 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157861850 | TTATAGTATGCCAGC[A/C]ACACCACTCTTGTGC | 51429 |
| rs553798866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157910869 | CAGGTGCAGTGGCAT[C/T]CCAGCACTTTGGGAG | 51429 |
| rs553802061 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SNX9, LOC105378078 | GRCh38.p7 | 6:157884766 | AGACAGCTTTGTTCA[A/T]CTCAGGAACCTTTCA | 51429 |
| rs553803822 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157795064 | AACTGAACAATCATA[A/T]GCAGTATGTGCACCT | 51429 |
| rs553827337 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157865448 | TTTGTTCTTCATGAC[A/G]CCCTGAGGGGAGCCG | 51429 |
| rs553839464 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157817362 | GTGGGTGGGCTTTCT[C/G]ATGAAAGCCCTGGGG | 51429 |
| rs553840254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157802004 | AGTTGAGCACACTGA[A/G]GTTTGGATGGGCTCA | 51429 |
| rs553846904 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157780918 | TGTATGACATGCAAT[A/T]CTGCACCCAAATTAT | 51429 |
| rs553855402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157871499 | CACTTGGACACAGGG[C/T]GGGGAACGTCGCACA | 51429 |
| rs553856637 | in-del | -/T | 0.0103295 | 0.0711199 | intron-variant | SNX9 | GRCh38.p7 | 6:157836206 | CCTCCTGCCTCAGCC[-/T]CCCAAAGTGCTGGGA | 51429 |
| rs553858984 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157818163 | ACATGATCACAAGGT[C/G/T]GCACAATAGGCCACC | 51429 |
| rs553881419 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | SNX9 | GRCh38.p7 | 6:157768870 | CATGGGGAAACCCCG[A/T]CTCTACCAAAAATAC | 51429 |
| rs553890467 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157772384 | TTGCTGGAATAGACC[C/T]CAAGTGGGCCCTAGG | 51429 |
| rs553930738 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157929707 | CTGTTCTTGTAATGA[-/T]TTTTTTTAAAGGTGA | 51429 |
| rs553939039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157899916 | GTGTGCGCGTGTATA[C/T]GTGCAAGTGCGTGCC | 51429 |
| rs553945016 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157941175 | CTGGGTTAAAAAAGA[-/T]TTTCTTCTGAAGCAG | 51429 |
| rs553950259 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157811467 | ATATTATAGTTGCTT[-/A]AAAAATAAAAAAGCA | 51429 |
| rs553951178 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157838810 | GTCCACTTTCCCTGG[G/T]TGTACTCTAAAATTT | 51429 |
| rs553979895 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157788483 | CACAATTCTGAAGAC[A/G]GTTAACTTCTTTTAC | 51429 |
| rs553982031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157796348 | GGACAGGCCAGGTTA[C/T]GACGTACAAGTTAAC | 51429 |
| rs554007338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157911606 | AACGGAAATCCACAG[A/G]CATTAAACAGGTTCC | 51429 |
| rs554020908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157938533 | AGGTATTTCCTGTTC[A/G]GTAGCAAATCAGTTA | 51429 |
| rs554029707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157860850 | TCCCCTAGAATTGTA[C/T]AGTCGCCTTTTGTTA | 51429 |
| rs554039198 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157795113 | CCAAATATGAAAATG[A/C]AATATAAAAACACAT | 51429 |
| rs554055887 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157892592 | CAGTTACTACACACC[G/T]ACAAATTATTGACCA | 51429 |
| rs554062363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157898820 | TAAGCCCAAAGCAGG[A/G]TGCAGGTCCCGGCTG | 51429 |
| rs554071056 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157812290 | TGGGGGAAAAGGGTA[C/T]CATTGGGGGCTATCT | 51429 |
| rs554075498 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157906053 | GGTTAAAACTGGTAA[A/G]TAAATGTAGACGAGA | 51429 |
| rs554075569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157899630 | AGAAAAAAAATTAGC[C/T]GGGTGTGGTGGCAGG | 51429 |
| rs554080243 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157844590 | TGGCTAATCCTTGTT[G/T]TTTTTTTTTGTTTTT | 51429 |
| rs554093255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157931640 | CATGCGAAGTCTGAC[C/T]GTTGTATTTTTCTCC | 51429 |
| rs554112418 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157776372 | AGGACAACAGCCACA[C/G]AGAAATGACACGTTC | 51429 |
| rs554141447 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157912374 | AATTCAGTGCTCTTT[G/T]AAAGCTTCAGAGAGT | 51429 |
| rs554145016 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157716802 | CAATGTGAAATTGGT[C/T]GCGTGCAGCAAACCA | 51429 |
| rs554149173 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157776963 | TCAAGGGCATTAACC[A/G]AAATCAGATATTAAA | 51429 |
| rs554156481 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157932411 | GGCTAGGCTGCCGCA[C/T]TAAGGACTTTTGCAC | 51429 |
| rs554178514 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157867085 | TTTTCAGTAGCTGGT[A/G]CTACAGGTGCTGGCT | 51429 |
| rs554186886 | snp | C/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889354 | GAGAATTGCTTAAAC[C/G]TGGGAGGCAGAGGTT | 51429 |
| rs554217233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157780191 | GTAAGCCTCCTGCTC[C/T]GTCCCTGCTTACTTC | 51429 |
| rs554223084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157784384 | TTTTTTTTTTTTTTT[A/G]GATGGCGTCTCACTC | 51429 |
| rs554235399 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157800321 | TTAGCAAAGACACAT[G/T]AAATACTTTAAAAGA | 51429 |
| rs554255688 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157882555 | CTGAAAAGGATTCAT[C/T]GTTCTGGATGCCATG | 51429 |
| rs554262987 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157831729 | CTTTTGTGCTAACTC[A/C/G]GCAGTGTGTTTCAAA | 51429 |
| rs554273684 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157915168 | GTGTCCATCCTTTTC[A/G]CTAGTCCTACACTGT | 51429 |
| rs554293150 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157716730 | ACTGAATAGATGGGA[A/C]AAAATCCATTAGGCT | 51429 |
| rs554300407 | in-del | -/T | 0.0755793 | 0.179102 | intron-variant | SNX9 | GRCh38.p7 | 6:157792151 | TTCCTTCCTTCCTTC[-/T]TTTTTTTTTTGATAC | 51429 |
| rs554301580 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157837729 | TGCATGAAGGCATGG[G/T]CATGCTGTCTGTGTT | 51429 |
| rs554303985 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157869227 | TGGGGTTCCCACGTC[A/T]TTCCACCTTCAGCCC | 51429 |
| rs554348690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157825205 | GTGATCCGAGATCGC[A/G]CCACTGCACTCCAGC | 51429 |
| rs554352615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157832681 | AGCAGGAAGAAGTGC[C/T]GAGCAAAAGGGGGAA | 51429 |
| rs554356509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157757405 | GGACACGCTCATTCA[C/T]TCAACAAACCTTCAC | 51429 |
| rs554365148 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157852675 | CCTCAACCTCCTGTT[G/T]AAGCGATCCTCCCAC | 51429 |
| rs554366535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157939774 | TTGAGGTTATCCAAA[C/T]TGAGAAATACAAAGC | 51429 |
| rs554367136 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157944818 | AAATGGAGATGGCAC[A/G]GGCTCCTCAGAGCGT | 51429 |
| rs554416931 | snp | A/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893768 | CAGTGATTCAAATGA[A/G]AATCAGTATTTTAAC | 51429 |
| rs554418670 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157719755 | AGAGTCAAGATGGCC[A/G]GGCATGGTGGCTCAC | 51429 |
| rs554428218 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157853097 | TCTAGTATCATTTTC[A/G]TTCTGGTAAAAGCAT | 51429 |
| rs554450854 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157768212 | TTTTCCTTCCTTTAC[C/T]TACATGGCAGAAGAC | 51429 |
| rs554485766 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157908999 | AGGCACATAGCAGTC[C/T]ACGGAAGAAAACAGC | 51429 |
| rs554494850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157929965 | AAAGTTTTATTGGAA[C/T]ACACCCATGCCCATT | 51429 |
| rs554510394 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157756432 | TAAAAAAAAAAAAAG[A/G]GTTAAATTGGAAAAT | 51429 |
| rs554532059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157820924 | TCGTGACCCGCCCGC[C/T]GCAGCCTCCCAAAGT | 51429 |
| rs554534203 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157740440 | GGACTAGAATCCCAG[A/G]ATAATTGAGCAAATC | 51429 |
| rs554537008 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821559 | CAGGATCTGGCGAAT[A/C]TTTCTCAGAAATTTT | 51429 |
| rs554544683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157724769 | CCACACTTTGGAACA[C/T]TGACTTTCATTCTTT | 51429 |
| rs554552584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157771173 | GGATTTATGACTGAG[A/G]TATGGGTCATTTATG | 51429 |
| rs554562366 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157836662 | GTGGCGCGATCTCAG[C/T]TCACTGCAAACTCCG | 51429 |
| rs554569498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157733552 | CCAGGTGGAAAGGCC[C/T]CCAAGATGACTTAGA | 51429 |
| rs554576645 | in-del | -/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157942904 | AATGCAATTCAAAAC[-/T]TTTTTTTCCCCTATT | 51429 |
| rs554579969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157815237 | TTTTTTTTTTAGACA[A/G]CGTATCACTCTGTTG | 51429 |
| rs554596245 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157765835 | TTTGGAAACAAGTAG[C/G]GTATGAGTCAGGAAA | 51429 |
| rs554625289 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157793196 | CTCAGATGATCCACC[C/T]GCCTCGGCCTCCCAA | 51429 |
| rs554625976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157921281 | ATTATTCTTGTCACA[A/G]TATGTGAATATGTTA | 51429 |
| rs554660573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157874849 | CAAAGAAGAAATCTC[A/G]AGAAATTAAAAAATA | 51429 |
| rs554663950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157835176 | TGCCACCACGCTCAG[C/T]TAATTTCTGTATTTT | 51429 |
| rs554683448 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157934594 | TTGTTTTCACTAAAC[A/G]TGTAGTCAATATCAT | 51429 |
| rs554689827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157747593 | GTTCGAGGCATATTG[C/T]AATACTGACTCAACA | 51429 |
| rs554691605 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157914513 | CAGGGTCTCACTGTC[A/G]TCGCCCAGGCTGGAG | 51429 |
| rs554703687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157864293 | TGAGGACAAAGCCTC[C/T]GTGACCTAAACGCCC | 51429 |
| rs554706460 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157786129 | CTCACTGTAGCCTTG[A/C]TCTCCTGGGCTCAGG | 51429 |
| rs554718638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157897381 | TAGGGCGAGGCATGG[A/G]GAAGGGACGCAGAGC | 51429 |
| rs554740551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157896776 | TTATTGAATTGAGTC[A/G]TGGTTTCCAAAAGTC | 51429 |
| rs554749919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157835605 | ATTGTAATCGCTGTA[A/G]TCTCCAAGTGTCACA | 51429 |
| rs554767038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157720378 | AGCCCATGGCTTTGG[A/G]AGAGGAAGGCCCCTC | 51429 |
| rs554768949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157848667 | TAGGTGGCAGATGCC[A/G]TGCTACCTGGTAAAT | 51429 |
| rs554774331 | snp | A/C | | | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157715622 | AAGAAAAGGGATATC[A/C]GTTTTATCTGTGTGT | 51429 |
| rs554788061 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890273 | TCTCCCCCACCCCTC[G/T]TGGCCATTCTCAGTC | 51429 |
| rs554795673 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157848324 | TTTTAGAATTGGCTC[C/T]GATGGCTTTAAGCAG | 51429 |
| rs554799477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157829685 | AGTTTTTATCATTAT[A/G]AAGTGAACCTCTTTA | 51429 |
| rs554819210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157760146 | AAAATGCTGGGATTA[C/T]AGGCGTGAGCCACCA | 51429 |
| rs554821227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157856896 | TCTTTGTGATGCACT[A/G]TGCTTAGATGAATTA | 51429 |
| rs554839053 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157870279 | CCCCACGCTCATGCT[C/G]TCACATATGCACTCA | 51429 |
| rs554849216 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | SNX9 | GRCh38.p7 | 6:157823432 | CCGGGGGACCCGCCC[A/G]CCATGGCCACCAAGG | 51429 |
| rs554869374 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157735413 | AGCCCAGACCTGGCC[A/G]GGCGTGGTGGCTCAT | 51429 |
| rs554882369 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157734488 | CAAGGGCCTTCACAA[A/C]ATTAGCTTCTCAGCT | 51429 |
| rs554882497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157727487 | TTTAATGAGGACTGT[A/G]GTACCAGAGTGATTA | 51429 |
| rs554887277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157830257 | AATTTCCATTGAGAA[A/G]GTATGTTGTTGGTAA | 51429 |
| rs554893488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157933203 | GGAGGCTGAAGCAGA[A/G]GGATCGCTTGAGCCC | 51429 |
| rs554896591 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157865005 | GCACTTTAGCCTGGC[A/G]ACAGAGAGAGACTCT | 51429 |
| rs554898582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157863638 | GACCATTTCTTTCAA[A/G]GACCACATGGAAAAT | 51429 |
| rs554899893 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157735386 | AACATCCTGTGGAAG[G/T]TGACAATTAAAAGCC | 51429 |
| rs554900222 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157937054 | TTAAAATTACCACTT[A/T]AAATGATTAGTTTTA | 51429 |
| rs554913458 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157721627 | CTGCAGGGAACCCTC[G/T]TCCCCACCGCGGCTC | 51429 |
| rs554926934 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157741187 | TCCCGTCTCTACTAA[A/C]AAATATAAAAATTAG | 51429 |
| rs554934706 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157736732 | ATCGTTGTCCTGTGC[G/T]GGTTTTCAGAGGGAA | 51429 |
| rs554936717 | in-del | -/A | | | upstream-variant-2KB, nc-transcript-variant | SNX9, LOC107986663 | GRCh38.p7 | 6:157714523 | CATGATAGCCTGGGC[-/A]CCTAGGATGACCACG | 51429 |
| rs554954123 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157843121 | TTGCAAAGGTGGTTT[C/T]AAGGAGATGAAGCCT | 51429 |
| rs554956709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157933635 | AGGTAACAAGTGGGT[A/G]ATGGAAGAGCTGAGA | 51429 |
| rs554964192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157923151 | AGAACTTGGAGTCAG[A/G]GCCCTTGAGTTCTGG | 51429 |
| rs554970043 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157784956 | TAGGAAATAGAAAAG[A/C]AAAGCAAAGGCCAGA | 51429 |
| rs554989178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157883283 | TAACCATAACTGTTA[C/T]GTACACTGGGGGACC | 51429 |
| rs555010180 | in-del | -/TA | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157804461 | AGGACTTGGTGAGTG[-/TA]TCTGTATTAGGGTTT | 51429 |
| rs555023797 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157937986 | AAATTAGCTTGCTGT[C/T]GAAATGTATGCCAGC | 51429 |
| rs555026482 | in-del | -/TT | 0.0146994 | 0.0844608 | intron-variant | SNX9 | GRCh38.p7 | 6:157738465 | GATTGCAACCCCTGC[-/TT]TTTTTTTTCTTTCCA | 51429 |
| rs555034414 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157804339 | TTGATTCTTAGTACT[C/G]CCACCCAAAATGTTC | 51429 |
| rs555052832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157754407 | TCTCAGTCATAATTT[C/T]GCAAAGGCAGTTTCA | 51429 |
| rs555055730 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894003 | CATTTCAAATCATGG[C/G]GGAAAGATGGATTGT | 51429 |
| rs555063643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157803533 | CATATATCCCACATG[A/G]CAAGAGATGCAAACC | 51429 |
| rs555077647 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157719490 | AGGACTTAAAGACAG[C/G]AGCAAACCCTTTTAA | 51429 |
| rs555082148 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157926349 | TGCACTGGATATTTT[G/T]GATTTGGGTACTCTG | 51429 |
| rs555097725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157760270 | GTTCAGTGACTTCTT[A/G]CTGACAGCTGGAAAT | 51429 |
| rs555108588 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157914575 | TTGACCTCCCGGGCT[C/T]AAGCAGTCTTCCAGC | 51429 |
| rs555113305 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157797540 | GATTGTCTAACTCTT[C/T]CTCAGAGCAATGATA | 51429 |
| rs555114898 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157856000 | ATGATCCACCCGCCT[C/T]GGCCTCCCAGAGTGC | 51429 |
| rs555126893 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157738574 | ACAGCACAGTGATGC[A/G]TCTTGACTCTTTATC | 51429 |
| rs555150328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157917086 | ATTTCCTTCATAGCT[A/G]TAGGACTATTCAGGC | 51429 |
| rs555180923 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157870627 | TCACCTGCCCTCACA[C/T]ATACCCACACTCTCC | 51429 |
| rs555196157 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157833220 | AAGAAGTTTTTTTAT[A/G]TTTTAGTTTGTTTTA | 51429 |
| rs555202430 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157840109 | CAGGCTGGTGCTTGG[A/G]GTGTCTTTGGATCTC | 51429 |
| rs555224182 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157782515 | GTGTATTGTAATCAC[C/T]ACAGTAACTACTAAA | 51429 |
| rs555276920 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157916933 | CATAGGATGAGTTTG[G/T]AACTATTCCCTCCTT | 51429 |
| rs555288577 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157738086 | TTAGAATAAGTGTGA[G/T]GTAGTGCTGAGAAGA | 51429 |
| rs555290794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157833535 | GAAAAAAAGAGTATG[C/T]TTTAAAAGTAGCTTT | 51429 |
| rs555291558 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157741531 | CTGGCTGCACACTGA[C/G]CCACACTGCAGTAAA | 51429 |
| rs555295127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157862141 | TTTGATAGCAGTTCA[C/T]TGAAACCGAGGAACG | 51429 |
| rs555300631 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157874021 | CGAAGGTTTCCTGAT[G/T]CCCTGTGAGTACAAC | 51429 |
| rs555301442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157796306 | TTATATTGGATCTGT[C/T]AGACCAGAGAAGAGA | 51429 |
| rs555329402 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157832581 | GAGATTTAAATGACT[C/T]ACAGTTCCAAAGGGC | 51429 |
| rs555331863 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | SNX9 | GRCh38.p7 | 6:157732789 | TTGGACTCAAGTGAT[A/T]TTCCTGTCTCAGCCT | 51429 |
| rs555360210 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157854213 | CCTGTCTCCCCACCC[C/G]CAGTGAGCATGCAGT | 51429 |
| rs555365179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157751195 | GCACTTCTTACATGG[A/G]GGTGGCAAGAGAAAA | 51429 |
| rs555388075 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886193 | GTCATCCAAACAAGC[A/G]CTTGCCCTGCTTACT | 51429 |
| rs555391564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157899511 | TATCTATATTTTCAC[A/G]CCTGTAATCCCAGCA | 51429 |
| rs555432102 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157861438 | ACTGTAGAAAGCGTG[C/T]TCATCAGGCTTTCCG | 51429 |
| rs555465206 | in-del | -/CA | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157870211 | ATACACATATGCACT[-/CA]CACATGCAAGCACAC | 51429 |
| rs555465476 | in-del | -/GAGCAGAATG | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157751769 | ATTCATAGGAACAAA[-/GAGCAGAATG]GTGGTTGCCAAAGTC | 51429 |
| rs555476020 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157877279 | ATAAAAGAAAAAAAA[A/T]GCGGGGGGGGCATCT | 51429 |
| rs555480732 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157845425 | CCCATTTGTCTTAAC[G/T]GTTGTCTCACTTACA | 51429 |
| rs555486396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157764417 | CAAAAGCCTTTGCTA[C/T]AAATGTACAGAGGAA | 51429 |
| rs555496391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157763030 | CAACAATCCTTATGC[A/G]TATTTGGGGGTTGCA | 51429 |
| rs555496637 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157717975 | CATTTGGAGTCTCCA[A/G]TGTCTATTATTTCCC | 51429 |
| rs555503478 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157873329 | AAATATGGAAACTAC[A/G]TTGAAATAGAACTAA | 51429 |
| rs555516904 | in-del | -/AAT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157740105 | AAGTATAATAATAAT[-/AAT]AATAATAAATCTTTA | 51429 |
| rs555528756 | in-del | -/TAA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157862300 | TTCTTCTGATGATCT[-/TAA]TAAGTCAAGATAAGA | 51429 |
| rs555538632 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157757320 | TGTCTAAGTCACCCT[G/T]CATGGGAGAGGCAGC | 51429 |
| rs555564871 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157867305 | GATCTCTAAATGCAA[C/T]GTGGGCAGCTGCCAG | 51429 |
| rs555570637 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157867752 | TATTTTTAAGATTTT[A/T]TTTTTTTGTAAGTTA | 51429 |
| rs555588155 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157882024 | AGAAGATGCCATCTA[C/G]GACTTGCACAGCTGG | 51429 |
| rs555645193 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157774730 | TTCTGCTCTCTTCGC[G/T]GCTCATCTCCCTTGA | 51429 |
| rs555688154 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157717436 | CTCGGGTCAGAGTGC[A/G]TGCCTGCTCTACCTC | 51429 |
| rs555695261 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157864935 | CGGGAGGCTGAGGCA[A/G]GAGAATTGCTTGAAT | 51429 |
| rs555701721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157880278 | AGTGCCGGACACATG[A/G]AAGATATTTCATAAA | 51429 |
| rs555702900 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157841339 | TTAGGAGAGGCACAA[A/G]ATAGAAATACAGATT | 51429 |
| rs555704350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157763933 | AGAGAGGATTTCTAC[A/G]GCAGTGGAAGAGAGC | 51429 |
| rs555729143 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157791771 | ATTGTTTTTCTCTTA[C/T]GCCTTTCTCAGCTTG | 51429 |
| rs555733209 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157838452 | TTCCATTAGGTGTAC[A/G]GTTGCTGTGGTAAAA | 51429 |
| rs555737245 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157900934 | AACCCTAAAGAGGCC[C/T]AGAAGAGCCCTGGCA | 51429 |
| rs555746407 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157767512 | GAAGTCTGTCCCTGC[A/T]TTATCGCGAACCTTC | 51429 |
| rs555757674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157940647 | GGTCTTGAACTCCTG[A/G]CCTCAGGTGATCCAC | 51429 |
| rs555764264 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157863474 | ACTTTTTGAAAGGAA[A/G]AGATTAGTTGTGGTT | 51429 |
| rs555774425 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157941102 | CAAAGGAGCCTAAAT[C/T]TTGGACAGGATTTTT | 51429 |
| rs555809119 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157895625 | TTTATGCTGTTAAGA[C/G]AAAAAAAAAAAGTAC | 51429 |
| rs555810424 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157766797 | AAATCTTTGTTTCCT[C/T]AACTGTAAAATGAGA | 51429 |
| rs555827609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157847708 | TCATAGGTTACACGT[C/T]GTCTATTCTGGTTTT | 51429 |
| rs555834090 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157864397 | CTCTAACCTTAGCAG[C/T]GAGTAAGTGCTTAGT | 51429 |
| rs555841089 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157720661 | AAGGGTGACGCTGAC[A/C/T]CTCTGAGAGGCAGAG | 51429 |
| rs555860482 | in-del | -/A/AAAAAAAAA | 0.227959 | 0.249026 | intron-variant | SNX9 | GRCh38.p7 | 6:157735252 | GCAAGACTCTGTCTC[-/A/AAAAAAAAA]AAAAAAAAAAGGACC | 51429 |
| rs555860927 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157913763 | GCAGTGTATAGTCTT[A/T]CGAGTCTGACTGCTT | 51429 |
| rs555872212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157725462 | TTTCCCACTGATACA[A/G]AACAGCTGGGCTTCT | 51429 |
| rs555879756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157775288 | GCTTGAACCTGGGAG[A/G]TGGAGGTTACAGTGA | 51429 |
| rs555883368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157735823 | AATACAAAATTGGCC[A/G]GGTATGGTGGCACAC | 51429 |
| rs555906650 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157929991 | CCATTTATTTGTATA[C/T]TGTCTTTGGCTACAT | 51429 |
| rs555924558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157906943 | CATCCTGGACTCAAT[C/T]GAGGATGAGGAAACA | 51429 |
| rs555952224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157745732 | TAATGAGCCCAAGGA[C/T]GAGAATATGAAAGAT | 51429 |
| rs555970522 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885887 | CATAAGAGCTGCGAC[A/C]ACTCACAGTATGTTT | 51429 |
| rs555986822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894691 | TTAAAAAGAAGTATG[A/G]AAGTCCCTTTCTATG | 51429 |
| rs555989486 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157941791 | TGTGCTTGATGTACC[C/T]AATGCATATTTGTGA | 51429 |
| rs556034160 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157761033 | ATCACCCTCGTATGA[A/C]TCACTAGTTACACTT | 51429 |
| rs556039199 | snp | C/T | | | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821435 | AAATCCTGGCTTTTC[C/T]ACATACTAGTGTGTG | 51429 |
| rs556052209 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157891132 | CGCCTTCCAGGTTCA[A/G]GCGATTCTCCTGCTT | 51429 |
| rs556070675 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157761799 | ATGACGCACACGTGA[A/G]CTCTTAAGACAGCTT | 51429 |
| rs556083881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157934884 | TCCCTGGCACCAATC[A/G]TAAGGTCCACGTCCC | 51429 |
| rs556086070 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157726359 | TCTTCCATGTCTCTC[C/T]TTAACTATTTGAACA | 51429 |
| rs556096987 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157779425 | AGCATGGACCTTCCC[C/T]GCAATTGCTTTGGAA | 51429 |
| rs556116777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157805927 | TACCCAGATGTGTAA[A/G]ATCAGGGCTATCTAT | 51429 |
| rs556124851 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157729070 | GATCACACCACTGCA[C/T]TCCAACCTGGGTGAC | 51429 |
| rs556145967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157897883 | TGGGAGGTGGAGCTG[A/G]AAGTTCCAAGCTTCT | 51429 |
| rs556162023 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157850210 | TGGTGATTGGATTTA[G/T]CAGTAAGAAAGCTGC | 51429 |
| rs556188820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157801598 | GCTAGGCATGGTGGC[A/G]TGCACCTGTAGTCCC | 51429 |
| rs556212030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157870248 | CCCTCAGACACTCTC[A/G]CCTGCTCTCTCACAT | 51429 |
| rs556235060 | snp | G/T | 0.039522 | 0.134904 | utr-variant-5-prime, intron-variant | SNX9 | GRCh38.p7 | 6:157823268 | GCCGAGCGCCCAGCG[G/T]CTGGGCCTGAGCGTC | 51429 |
| rs556245339 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157816096 | GCCTCCTAAACTCCT[A/C]GAGTGCCAAGCACCA | 51429 |
| rs556248205 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157870808 | GCAAGCACACACACC[A/C]CTCAGACACTCTCAC | 51429 |
| rs556255041 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157813298 | ACTTGTCAGCCACTG[A/C]AAACCCCAAAAGGTC | 51429 |
| rs556259141 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157909261 | ATTTGGTATTGTTGA[A/C]AAATCAAAATGTGTA | 51429 |
| rs556268257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157742783 | ATGTGATTATTACAT[A/G]CGTAATGTACACATT | 51429 |
| rs556268543 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157843170 | GCTTAGGTGGTGCCA[A/G]CAATGGGAGGATGCT | 51429 |
| rs556278123 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157754319 | GTTAGTTCAGCTTAC[A/G]CCCAGGAATGAACAC | 51429 |
| rs556302242 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157815861 | CATGGACACAGGGAG[C/G]GGACCATCACACACC | 51429 |
| rs556316395 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157793398 | AAAAATATTCCCCAT[-/C]CCCCCGCCAAGTTTT | 51429 |
| rs556327543 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157773043 | GAGGGAAAGTGATGA[A/T]GTCGTCACTAAGGCA | 51429 |
| rs556334407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157810848 | CAAGACTGGAGGATC[A/G]CTTGAGCCCAGGAGT | 51429 |
| rs556349068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157937763 | AGTTGTGAGTATTTT[A/G]TATTTTATGTCAACC | 51429 |
| rs556353615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157794947 | CAAAAAAGGAAAAGA[C/T]TTGGAAGAGCAGAAT | 51429 |
| rs556354969 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157716033 | CAAAGAACTAGTGAG[C/G]CATTTCCCCAAAAAA | 51429 |
| rs556362509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157924760 | TGACTTCCGTATCTC[C/T]TTTACTAAACTAATG | 51429 |
| rs556373825 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157802404 | TGACTTTCCTCGTGT[A/G]TAGGATGGAGGTGAT | 51429 |
| rs556379683 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157777368 | CTGGGAGACAGAGCG[A/T]GACTCCATTTAAAAA | 51429 |
| rs556380940 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157874615 | TGCTTCATCAAACCA[A/C/T]AGCAGCATACACATT | 51429 |
| rs556389646 | snp | A/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887697 | GTTTTCATTGGGAGC[A/G]TAAACTGGGTCCCTG | 51429 |
| rs556389700 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, downstream-variant-500B | SNX9, LOC107986663 | GRCh38.p7 | 6:157715142 | GGCTGAAAGAATTGC[A/G]GCCGTGAATAAACAT | 51429 |
| rs556401777 | snp | A/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889687 | AAATATCTTAAGCCT[A/G]TTATCTCTTCAATTA | 51429 |
| rs556421523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157917404 | GTTTTGAGATATTTC[C/T]GCTATCACAGGCATT | 51429 |
| rs556445155 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157943843 | CTTGGCTTGGGTGGC[A/G]GGTTCATGGCCAGTT | 51429 |
| rs556445845 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157835868 | GGGCAGTTCTTTATA[C/G]CCGTGTGAAAACAGA | 51429 |
| rs556460225 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157850874 | GCTGAATAAGGCTAA[C/T]GCCATAGAAGGAAGG | 51429 |
| rs556475440 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157772552 | ACAGACGAGGTGAGG[A/G]CGAATCCTTCCCCAG | 51429 |
| rs556484131 | in-del | -/A | 0.325563 | 0.238307 | intron-variant | SNX9 | GRCh38.p7 | 6:157912420 | TACTAAGATTTGTTT[-/A]AAAAAAAAATAAGTT | 51429 |
| rs556496420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157851919 | GTCTGGCTTATTTCA[A/G]TTAGCGTAATGTTTT | 51429 |
| rs556497526 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157783088 | AAAGATGTTATTATG[A/G]AAATGATAAGCATAA | 51429 |
| rs556498340 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157724675 | ACCATTTGTGACTAC[A/G]CATTAAGCCTTGTAT | 51429 |
| rs556500083 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157809709 | CTATATTATATGATG[C/G]TCAACATTGTTTGTT | 51429 |
| rs556530820 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | SNX9, LOC107986663 | GRCh38.p7 | 6:157714370 | TCAATAAACAGTTTC[A/G]CCAACTGCTCTTTCT | 51429 |
| rs556538621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157843258 | CCTTGAACAATGTGG[A/G]GGTTAGGAGCACCGA | 51429 |
| rs556547773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157871394 | TCAAAAAAAAGAAAA[C/T]CACTGGGTAGAAAAA | 51429 |
| rs556548692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157913947 | ATGAATAAAGCTGCC[A/G]TAAACATTTGCATAC | 51429 |
| rs556563374 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157736676 | GATTGCCCTGGCCAG[A/C]ACTTCCAATACTATG | 51429 |
| rs556570430 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157844896 | CACTGCGCCTGGCCG[A/T]CGTCCTTGTTTTAAA | 51429 |
| rs556629592 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157869863 | CCCCCACACACACTC[G/T]CACACACCCTTATGC | 51429 |
| rs556654963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157838106 | CAGCCCCAATTTCCC[A/G]GGCTCGAACAATCTT | 51429 |
| rs556668814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157867402 | GCAGATGAGTCATTT[C/T]GGTAATGTCTTCCTT | 51429 |
| rs556670777 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157723960 | CAATTCCATTCTGCT[A/G]ATAACTTCTGGAGTA | 51429 |
| rs556670829 | in-del | -/TGTT | 0.0166589 | 0.0897325 | intron-variant | SNX9 | GRCh38.p7 | 6:157866946 | AATGAAATAGGTGTT[-/TGTT]TGTTTGTTTGTTTTT | 51429 |
| rs556714324 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157874668 | TTCTCTAAGACAGAC[C/T]ACATATTCTGAGCCA | 51429 |
| rs556715016 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821390 | TAAAAGAATATGGAA[A/G]ACTCATTACTTATGA | 51429 |
| rs556722971 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157851288 | TAAAATAAATAAATA[C/T]AAATAAACCTCTACA | 51429 |
| rs556740520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157742112 | ATAGCACTGCTAACT[C/T]GGAAATCTCTGCTGC | 51429 |
| rs556744201 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157944219 | CTGACCTAATAATTA[C/T]GGGAAATGGAAAGTC | 51429 |
| rs556776786 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157820218 | GGAGGCTGAGGCAGA[C/T]GGATCACTTAGGATA | 51429 |
| rs556789035 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157825075 | CAATATGGTGAAACC[C/G]TGTCTCTACTAAAAA | 51429 |
| rs556789550 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157934924 | AACCAGGGTTCCTAT[A/C]AAAAGACTTAGATAC | 51429 |
| rs556801201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157773492 | AGTAAGAGGTTCAGC[A/G]TAAGTTTTCCTGAGG | 51429 |
| rs556814220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157859841 | TTAACACTTTGTGAT[A/G]TGAATTGAAAATACT | 51429 |
| rs556824810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157928417 | GAAGTTAAAATATAA[A/G]TCAGCGCTTTTTAAG | 51429 |
| rs556835323 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157727389 | TTCGTTTCAACTAGA[A/C]GATCAGAGGCCAAAA | 51429 |
| rs556851642 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157771082 | CCTGTAGGCTCTGAA[C/T]CAAATAGTTATTAGT | 51429 |
| rs556865515 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157737357 | GTCTGTTCAGGGATT[C/T]GACTTCTTCCTGGTT | 51429 |
| rs556866955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157736965 | CGTTTATTGATTTGC[A/G]TATGTTGAACCAGCC | 51429 |
| rs556884013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157727693 | GGGAGAAGACTGTGT[A/G]GGAAGTGTGTTTCAT | 51429 |
| rs556885017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157874270 | CTTTTCCATACAACT[A/G]CAACCCCCTATTCAC | 51429 |
| rs556887975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157866296 | TGAAATAAAAATTTC[A/G]TTTAGGGCTGGTCAT | 51429 |
| rs556929034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157828486 | GTTAAGTTTTTATGA[C/T]TATGATTATTATTAT | 51429 |
| rs556930354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157827925 | CATGTGTTACACAGC[C/T]TGTCTGGTTAAATTA | 51429 |
| rs556954261 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157936197 | AATCATGGTTTCTTA[A/G]GTTAAGACAAAGTGG | 51429 |
| rs556961793 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157776293 | CCACCATCCAGCCTG[A/T]GGTTCCTCCATGGGC | 51429 |
| rs556977306 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157739312 | AGACACTTCTCAAAA[G/T]AATACATTTATGCGA | 51429 |
| rs557021923 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157867883 | AGTTATGTATGTAAT[C/T]GAGTTTATTATGTCT | 51429 |
| rs557034694 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157758478 | CAAGTCTGGGGATAG[A/G]AGAGCAGTGAGGAGC | 51429 |
| rs557040421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157866779 | CATTTTAATAGCAAG[C/T]GATTCTTCTAAAGAT | 51429 |
| rs557052366 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157744818 | GGCATGATCTCTGCT[C/G]ACTGCAACCTCCGCC | 51429 |
| rs557054717 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | SNX9 | GRCh38.p7 | 6:157820643 | TATGTTCAAGATCCC[C/T]TCGGTGTGGCTTATT | 51429 |
| rs557067956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157834525 | CAATTTTTTAAATTT[C/T]TTTTTCTTTAGTAGA | 51429 |
| rs557071721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157799963 | TTTTCAAGCATCCCA[C/T]AGGCATTCATGAGGG | 51429 |
| rs557091175 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157796192 | AATATAAATATGCTC[A/G]CAATGCTGTTTCTTG | 51429 |
| rs557118319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157841279 | AAATTCCACATCTGT[A/G]TGTTTTAATTTAGGG | 51429 |
| rs557119211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157901117 | CTGCACATCCATTCA[C/T]AGGCTCTCTGCAGGG | 51429 |
| rs557139529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157727866 | CAGCTGGCCCAGAAG[C/T]GGGTAGAGATATAGG | 51429 |
| rs557158500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157869816 | CGTGCACCCATGTAC[A/G]TACTCTCACGCACTC | 51429 |
| rs557170185 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157827425 | TATATTATAGTTTAT[A/G]TAATATATAAACATA | 51429 |
| rs557178219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157806612 | TAGCATGCAAACCAA[C/T]TGTTTGTTTGTTTTG | 51429 |
| rs557193504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157836046 | AAGCAATCCTTCTGC[C/G]TCAGCCTCCCAAGTA | 51429 |
| rs557203093 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157733028 | ACACCCTCTAGGTTC[A/G]TCTGTGTTGCTGAAA | 51429 |
| rs557207326 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157770605 | ACCCTGGCTAACACG[A/C/G]TGAAACCCCGTCTCT | 51429 |
| rs557214596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157848573 | AAAGAAACTGTACTT[C/T]CTGTACTTTGAAAAC | 51429 |
| rs557226894 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157742640 | TGGATGATCGAGTGG[A/C]TTTAGGAACCACAGG | 51429 |
| rs557248701 | in-del | -/GGGCGGGTGGGGGTC | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157823887 | ACCCTCGCCCCCGCG[-/GGGCGGGTGGGGGTC]GAGACCTCGGCGGAG | 51429 |
| rs557257803 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157829557 | TAATTGTGTTCCTCT[A/G]TTTGATCTGTTGTAT | 51429 |
| rs557258118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157907758 | GAGGAAAGCCACCGC[A/G]TCTTCAGGAGGCCCA | 51429 |
| rs557261263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157739865 | AGAAAACCAAACACC[A/G]CATGTTCTCAGTCAT | 51429 |
| rs557281694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157868564 | ACATAATATTCATTT[A/G]TGTCCAATCTTCTTT | 51429 |
| rs557325032 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157849154 | CTGGAATTTATCATT[A/G]AAGGTAAGAATTGTA | 51429 |
| rs557341463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157929242 | GTTTGTAGGCTTTCA[C/T]TCTGCTGAAGGTTTT | 51429 |
| rs557356640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157844662 | GCAGTGGTGCAATCT[C/T]GGCTCACTGCAGCCT | 51429 |
| rs557393034 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157806040 | CCACTGTAGTCTGTG[A/C]GTTGAAAGTTATTAT | 51429 |
| rs557403482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157848015 | GGCAAGACCCCTCCT[C/T]ACCTGCCTGCTGTAA | 51429 |
| rs557410934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157923017 | AAAGCATTTCTGAAG[A/G]TCATGTTTTCTGCAT | 51429 |
| rs557426619 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157943743 | AGAAGGAGGGCACCC[A/G]GCACCCCGGCGTCTC | 51429 |
| rs557430419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890251 | CCACCATGGGTGTGC[A/G]TGTCCGTCTCCCCCA | 51429 |
| rs557452870 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157895842 | AGTTCCTTGTGCTAG[A/G]TGCTCCATAGTCAAA | 51429 |
| rs557480805 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157719683 | ACACCGTAGCTCAGT[A/G]ATGCTCAAAGGAAGG | 51429 |
| rs557488866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157932536 | TTTTGTTTCAATGCC[A/G]TCAGTTTCATTTCTC | 51429 |
| rs557510690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157744129 | ACAACTAATCTAATG[C/T]CTATAATATGGTAAA | 51429 |
| rs557514192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157896640 | GTAAAATTAGATTGA[C/T]GCTACCTTTTGTGCT | 51429 |
| rs557522481 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157760118 | CCTCGTGATCTGCCC[A/G/T]CCTTGGCCTCCCAAA | 51429 |
| rs557535930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157809932 | TAAACATCCTCTTAT[C/T]ATATGATCACTCAAT | 51429 |
| rs557545865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, nc-transcript-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157892980 | CTCCATTTCACAGCC[A/G]GTCCTTGATGGAAAC | 51429 |
| rs557561355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157872581 | CTGGCTTTGAATGGG[A/G]CAACAGGGAGACTGG | 51429 |
| rs557565623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157761979 | CTTGAGAAACTGGAT[A/G]AACGTCGCAGCAGGA | 51429 |
| rs557568936 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157877425 | TAAATCAAGTAAAAA[G/T]ATTTTAACTGCTATC | 51429 |
| rs557569424 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157769455 | TTTCTCCTGGTCTGC[A/G]GAGGAAGGGAAAGCT | 51429 |
| rs557572147 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157802105 | TTCTTCAGATATCTG[A/C]GGGTTCTTATGGCAT | 51429 |
| rs557613188 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157922172 | CTGCCTGCCCCTGTG[G/T]CCTGTAGTCTGCCAG | 51429 |
| rs557629098 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157780302 | ACACTCACATGTAAT[G/T]CTCCTGATAAAGCTA | 51429 |
| rs557649435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157737573 | TCTGGCTGGTGTTCT[A/G]TCTATTTTGTTAATC | 51429 |
| rs557650162 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157741333 | GTCTGGGTAACACAG[C/T]GAGACTCTGTCTCAA | 51429 |
| rs557657092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157839584 | GTCCAAGTGGGGGAA[A/G]AATTATAATTTTGCT | 51429 |
| rs557663034 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157763120 | TTCATTACCTAGAAA[C/G]TGAGGGAAGTCACGC | 51429 |
| rs557682071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157867248 | GTGTGAGCTGCTGCA[C/T]TCAACCAAAATAGGT | 51429 |
| rs557689553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157883246 | TATACATAATGCTCT[C/T]GCACACTTATACGGT | 51429 |
| rs557697204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157851879 | CAGGTCTGAGCCACC[A/G]TGCCCGGCCTGTTTG | 51429 |
| rs557701628 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157766017 | ACACACATATTTTCC[A/G]GAAGATTTTAATAAA | 51429 |
| rs557703922 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157793099 | TACAGGCATGTGCCA[C/G]CACACCCAGTCAGCT | 51429 |
| rs557707764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157785359 | AAGAAAATGATAAAC[C/T]AAAATACCTTATGAA | 51429 |
| rs557739264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157770143 | AGCTAATGGTACGTG[A/G]ACTCCATCCAAGGCC | 51429 |
| rs557741082 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157763196 | ACCGTCCCAGGTGGG[C/T]TCCACCTCTGCCCTC | 51429 |
| rs557752309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157925484 | CACTCCTGGATATGT[A/G]CTGAATAGAAATGCA | 51429 |
| rs557774456 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157910802 | AGACTCTGCTACTCT[A/G]TGTAGTCACTGAGGG | 51429 |
| rs557792716 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157904773 | AGCCTAATTCATTAA[C/G]CATTCAGTATGCTCC | 51429 |
| rs557798148 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157738037 | TTGTTATGGTTTGCT[A/G]AGGAGTGTTTTACTT | 51429 |
| rs557807758 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | SNX9 | GRCh38.p7 | 6:157751029 | GGAATACAAAATGGT[C/G]CAGCCACTATGGAAC | 51429 |
| rs557819842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157860049 | TGTGGTGGCTTTTGC[A/G]CTGCGGCAGCAGAGA | 51429 |
| rs557822765 | snp | A/G | 5.01199e-05 | 0.00500574 | missense | SNX9 | GRCh38.p7 | 6:157873171 | GTTCCCACAGACTAC[A/G]TTGAAGTAAGAGCTT | 51429 |
| rs557833864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157810670 | TTCAGGAACGGAACC[C/T]TTGATGTTGGGTTTT | 51429 |
| rs557834931 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157738565 | CTCCTGAATACAGCA[C/G]AGTGATGCGTCTTGA | 51429 |
| rs557846861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157898376 | AGGGCCCCTGCTGTC[A/G]CCCGTGGATCACTGC | 51429 |
| rs557869787 | in-del | -/AAA | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157775359 | GAGACTCTGTCTCTC[-/AAA]AAAAAAAAAAAACTT | 51429 |
| rs557887481 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157725417 | CTCCTCCACTTCAGG[C/G]ACCTTAATTATGGAT | 51429 |
| rs557892168 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157852541 | AAGAACTCTGTAACA[A/G]TAGACCTCTATTTCC | 51429 |
| rs557908365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157898831 | CAGGGTGCAGGTCCC[A/G]GCTGAAGGCTGGCAG | 51429 |
| rs557914427 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157762536 | AGTTTAGTATCATGT[C/G]TATTTAATATGCACA | 51429 |
| rs557936757 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157789279 | ACCTTTTATATAAAT[G/T]TATATATTGCCACAA | 51429 |
| rs557938124 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157904135 | TAAATATACTTGAGC[A/G]CTATAAGAATTCACC | 51429 |
| rs557955978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157782099 | TTACTAAAAAACCCT[A/G]TCTACTGTTAGTTTC | 51429 |
| rs557958245 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157790244 | AAAAAACAGGTATCA[A/G]GGTAAAACCTGCAGT | 51429 |
| rs557969102 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157793198 | CAGATGATCCACCCG[C/T]CTCGGCCTCCCAAAG | 51429 |
| rs557975769 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157924778 | TACTAAACTAATGAT[A/G]TTTTTAAAAAGATTG | 51429 |
| rs557976761 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157828880 | CCCGACTGCCATTTT[A/G]TATTTGTTTCTATAA | 51429 |
| rs557980660 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157838932 | GGCCGAGGACATAGC[A/G]TCTTGGAATGGTTAA | 51429 |
| rs557980800 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157865086 | GGCTCACGCCTGTAA[G/T]CCCACACTTTGGGAA | 51429 |
| rs557984153 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157748362 | GTTTTACAAATGCCA[A/G]TGTAAAATAAGAGAA | 51429 |
| rs558004854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157905652 | AAAAGAAACAAGCAC[A/G]TATGCTGATGAGCAG | 51429 |
| rs558008765 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157826670 | ATACAAAAGCTGCAG[A/T]GCATTTTAGTCTTGA | 51429 |
| rs558020600 | in-del | -/CACCA | 0.00119737 | 0.0244387 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890224 | CAGCTTTCCTACACT[-/CACCA]CACAGCACCACCATG | 51429 |
| rs558036886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886045 | TGGAGACAGACAGAC[A/G]TCGTGGTGCCATTGC | 51429 |
| rs558045961 | in-del | -/TCTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840487 | TTCTCTCTCTCTCTC[-/TCTT]TCTTTCTCTTTCTTT | 51429 |
| rs558079665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157926182 | AAAGAAATGAAAACC[A/G]TAAGAGAGAGATTAC | 51429 |
| rs558089663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157758782 | TAGCAGGTAATGGGT[A/G]TCTGAGAAGTATTTA | 51429 |
| rs558095123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157771840 | GAGTAGCTGGGATTA[C/T]AGGCACCCACCACCA | 51429 |
| rs558097868 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157798317 | TCAAACCCAAACTGA[C/G]CAACATTCTAGAAAG | 51429 |
| rs558098905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157796243 | TTTCCTTAAACTGCC[A/G]ACGGAATGGTGTTTG | 51429 |
| rs558114638 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157728010 | TATAAACCTCTCCAT[A/G]GCCTCAAGTTGTCGG | 51429 |
| rs558140021 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157798975 | ATTATGAACAAAAGA[-/G]GTTTAATTGACTCAC | 51429 |
| rs558143672 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157724869 | TGACCCTTTTGATTA[C/T]TTTAGGTTGACGATA | 51429 |
| rs558147478 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157861338 | CATGATAATTAATTG[A/C]CCCGCATCCCCTTGG | 51429 |
| rs558159212 | in-del | -/A | 0.303938 | 0.244112 | intron-variant | SNX9 | GRCh38.p7 | 6:157744016 | GAGAGACTCTGTCTT[-/A]AAAAAAAAAAAAAAG | 51429 |
| rs558169458 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157930939 | AATTTTACAATTGCA[-/T]TTTTTAAGGATATCA | 51429 |
| rs558184358 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157825973 | AGTATTAACTGATGA[A/C]AAGTAAATTCAGTAT | 51429 |
| rs558203044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157716848 | TCACGTTGCCCATAA[A/G]TGATTCATGCCATGC | 51429 |
| rs558208669 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157746521 | TAAGTATCAAGGGGC[C/T]GTATTTCTGCCCAAT | 51429 |
| rs558238568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157869256 | CCATTTCTTTACACT[A/G]TGCGGTCTCAGATTT | 51429 |
| rs558256131 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157912547 | TGAGCCAAGGAAGCC[A/G]AACAGCACAGAAGGG | 51429 |
| rs558258083 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157919326 | TCACTCTCTCTTCTT[C/G]CTCTGGGATTCTCAT | 51429 |
| rs558304258 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157864328 | TTTGCCGCACCTCCC[A/G]ATACCACTGCCTTGG | 51429 |
| rs558312101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157897784 | GCCTCCCAAAGTGCT[A/G]GGATTACAGGTGTGA | 51429 |
| rs558321441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157912988 | AGAAAAATTTTCACA[A/G]GAATAATTTTTGAAT | 51429 |
| rs558323553 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157818942 | TCCTGGACTGCTCAG[G/T]TCCTAGCAGTCAGAT | 51429 |
| rs558352069 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157752223 | CAGGATTGAAGGGGT[G/T]GCCTGCCCCTCCACA | 51429 |
| rs558373590 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157891100 | GTAGTGGTGTGAACT[C/T]GGCTCACTGCAACCT | 51429 |
| rs558384456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157847127 | TTTGTTTTTGAGACA[A/G]GGTCTGGCTCTGTCT | 51429 |
| rs558391052 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157899925 | TGTATATGTGCAAGT[A/G]CGTGCCTGTGGGTGT | 51429 |
| rs558394318 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157911885 | TTCAAATTGTCATAG[C/T]AAAATTGAAAATGGG | 51429 |
| rs558415316 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157734518 | TGGGAGGCAGCAGCA[A/C]CCAAGGACCTAGGAG | 51429 |
| rs558419102 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime | SNX9 | GRCh38.p7 | 6:157766415 | CCCCACCTTGCACTG[A/C]GGTGCGTGGAAGTTG | 51429 |
| rs558433936 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157804458 | TCAAGGACTTGGTGA[G/T]TGTATCTGTATTAGG | 51429 |
| rs558447126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157897424 | CTGCCCCAGGTGCCC[C/T]TACATGTTCAGCACC | 51429 |
| rs558462673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157758294 | AAAAAAGAAGCAGAT[A/G]AGGCCAGGTCACCTA | 51429 |
| rs558483976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157939895 | GGTTTGGGAGAAGGC[A/G]GCATAGGAGGCATCC | 51429 |
| rs558495295 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157812963 | TTGCAGATCAGAGAG[A/G]ATATAGTGACTTTGT | 51429 |
| rs558498704 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157863666 | AATAGATGGCAGTTG[G/T]GGTTGAGGCCAGCAC | 51429 |
| rs558519927 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157717353 | ACCCCACCCAGCCTA[A/G]CTAAGTTACTCTTTA | 51429 |
| rs558526167 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157846245 | TTAGCTCTTCAAATT[G/T]TATTTTATTTTTCCA | 51429 |
| rs558535449 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157815764 | GAAGCTGGAAACCAT[A/C]ATTCTCAGCAAACTA | 51429 |
| rs558540248 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157916401 | ATTTCATCTTTTCCA[A/G]TCCATGGGCCTTCTA | 51429 |
| rs558545125 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157783641 | TCTAAATACCTCCTT[-/C]TTTTTTTTTTTTTTT | 51429 |
| rs558550064 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157774449 | AGATAAGGAGGGGGG[C/T]TTCCAAGGTGAAGTG | 51429 |
| rs558571102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157856987 | TGCTTGTAAAAGAGA[A/G]ACTTTTATCTACTAC | 51429 |
| rs558575561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157807650 | GGATTTGCATTTAGG[C/T]CCCAAAGGCTAGGGG | 51429 |
| rs558607474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157760424 | CATCCACATTTCTCC[C/T]CCAGAGAGTGTCCAA | 51429 |
| rs558607990 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157728698 | GCAGGTGAAACAGTT[A/C]CTTCTAGAAGGGACC | 51429 |
| rs558613599 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157733094 | GAGGGGACTTCCAGC[A/G]TTTCCCAAGGTTCCG | 51429 |
| rs558641837 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157786715 | ATACTTTGGGATAAA[A/T]TTAACAAAAGATGTG | 51429 |
| rs558659137 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157922874 | AAGTTCTTTGAATTC[A/C]GTAAATATTTGGGTT | 51429 |
| rs558676060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157936496 | CCTGGGTGACAGAGC[A/G]AGACCCTATCTCAGA | 51429 |
| rs558680498 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157857667 | TTTTTTTTTTTTTCC[A/T]TGAAAAAGATTGGGG | 51429 |
| rs558689433 | snp | A/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894649 | ACTATTAAATTACTC[A/G]AAGGAATTATGGGAG | 51429 |
| rs558698213 | snp | A/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157892223 | AGTTAGGGAACTACC[A/G]AGGGGATTTGGGAGT | 51429 |
| rs558734918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157760946 | CACAGCCGGGGGAAA[A/G]GAGATTTATTTTACA | 51429 |
| rs558745032 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157801490 | TCCCAGCACTGTGGG[A/C]GGCTGAGGCAGGAGG | 51429 |
| rs558746336 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157722957 | GCAGTGAGTCAAGAT[A/C]GTGCCACTGCACTCC | 51429 |
| rs558746871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157849338 | AGCCTCTTTATAAGC[C/T]ATGCTTATTAACATT | 51429 |
| rs558764127 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157930665 | GAGCCCTTATGAGAA[A/T]CTAATGCCTGATAAT | 51429 |
| rs558800689 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157917308 | TATTATATTGTTTCT[C/G]CTCTTTTATCATTTC | 51429 |
| rs558809976 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157850129 | GGGAGGAGAGTGTTT[C/G]AAGAAGGAAGAGTGG | 51429 |
| rs558810331 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157842719 | GAACTGGTTGGGCCA[C/G]GTTACTGGTCTGAGT | 51429 |
| rs558815827 | in-del | -/AAAT/AAATAAAT | 0.037967 | 0.132446 | intron-variant | SNX9 | GRCh38.p7 | 6:157911120 | CTGTCTCAAATAAAT[-/AAAT/AAATAAAT]AAATAAATAAATAAA | 51429 |
| rs558827152 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157918099 | GTCTGTAGCAGCTGG[G/T]TGGAGTGTTTCATTC | 51429 |
| rs558862062 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157824248 | CTACCTGAATTTTCA[A/G]AAGCCACCCTCCCCC | 51429 |
| rs558878307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157884601 | CTCTCACTCCCACCC[C/T]CCCGTATGAATTCTT | 51429 |
| rs558882702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157904202 | GCACTTTGGGAGGCC[A/G]AGGCAGGCAGATCAC | 51429 |
| rs558889874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157754710 | TCTCACCTGTGCAGC[C/T]ATCACAACCTCAAAG | 51429 |
| rs558895573 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157731261 | CTCCTGAAGTGCTGG[G/T]ATTGCAGATGTGAAC | 51429 |
| rs558924747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157837944 | TTGGCTGTGGTTAAC[A/G]TTAGAATATTATTAT | 51429 |
| rs558929549 | in-del | -/G | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157756117 | CTCAGTGGTTTGCTT[-/G]AAAGGGTTAAATTAG | 51429 |
| rs558939379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157878044 | TCATAAATGTATAAC[C/T]TACTATGTAAGATAG | 51429 |
| rs558940648 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157826220 | AGAAAGTTAATCAGG[A/G]TCGGGCGCCGTCTCA | 51429 |
| rs558954165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157764210 | TCCAAGTCATTACCC[A/G]GCTCATGGTCATTGG | 51429 |
| rs558969715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157735976 | AAAAAAAAAAAAAAA[A/G]AAAATCCCACCTGAG | 51429 |
| rs558972015 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157741570 | GCTGCTGTTATCAGG[C/G]AAAACCTGAGCATGG | 51429 |
| rs558991852 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157846162 | CCTCTGTCAGCTGCT[A/G]TTAGGCAAAATCTCT | 51429 |
| rs559016343 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157832120 | GTGTTTAAGGATGCT[A/G]TTCAGTCTGACTGAA | 51429 |
| rs559019251 | snp | G/T | | | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822098 | ATTTATGCATATTAT[G/T]ATGACTATAGCTTAA | 51429 |
| rs559021169 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157870327 | ACACCTACTCTCTCA[C/G]CTGCGCTCACACTCA | 51429 |
| rs559031653 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157810922 | AAAAAATAAAAAAAT[C/T]ATCCAGGTGTGGTGG | 51429 |
| rs559037062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157781502 | TCTTACAAAATTCTC[C/T]GGAAAAGGATGATTG | 51429 |
| rs559040416 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157742297 | GGAAGGAAGCTATTA[C/T]GGGTTGGGAGAGGTT | 51429 |
| rs559053290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157931313 | TTTCCTGATAACTGC[A/G]GCTTATAGACCTTAC | 51429 |
| rs559064384 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157738176 | GTCCAGAGCTGAGTT[C/G]AAGTCCTGAATATCC | 51429 |
| rs559067430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157730382 | ATACAAAAATTAGCC[A/G]GGTGTGGTGGTATGC | 51429 |
| rs559080704 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157916058 | TTTTTTGTTTGAGAC[A/G]GAGTCTCGCTCTGTC | 51429 |
| rs559091533 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157802817 | CTTGGTGGGCCCCCC[C/T]GAACTTTCCAGTAGA | 51429 |
| rs559096721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157852825 | GCGATCTGTCCACCT[C/T]GGCCTCCAAAATGCT | 51429 |
| rs559102392 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157911425 | GCAAGAGTCGAGAGA[A/T]ACAGTTCAGGGAGGG | 51429 |
| rs559107112 | snp | A/G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157848196 | TCCCCCTAGAACAGC[A/G/T]TTCATGGTACTAACT | 51429 |
| rs559139918 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157788099 | TTATTCCTACTATAC[A/T]GATGAAGAAATTGAT | 51429 |
| rs559151336 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157873047 | ACACAAAATTTCTCC[A/G]GGAAATCTCAACTGT | 51429 |
| rs559156752 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157853608 | ATAGGTGACTAACTG[C/G]GTAGGGGAATGTCTG | 51429 |
| rs559157162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157830809 | TGAAAATTGCCTTTT[C/T]TCCATTCTTTCTTTC | 51429 |
| rs559165800 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157918432 | ACTCCATTTCTGTTA[C/T]GGTTACTGTTTGTAT | 51429 |
| rs559175259 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157839700 | TTGCCCAGGGTGAAG[C/T]ATAATTTGAGGGTGG | 51429 |
| rs559186109 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157914714 | AAGTCCTGAGCTCAA[A/G]CGGTCCACCCACTTC | 51429 |
| rs559198505 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157916505 | CTTTGGCTTATTCCT[C/G]ATCTTAGGGACAAAG | 51429 |
| rs559207768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157731876 | GGATGGCAGTCTAAT[C/T]GGAATGATCCCTGTC | 51429 |
| rs559222011 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157744291 | CAATGCCTCTGTGAA[C/T]GCACCATCAGGCCCC | 51429 |
| rs559226126 | snp | A/C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157779571 | TGTATGTGTTCGAGT[A/C/T]GCAGGGCCTGGGTTG | 51429 |
| rs559229195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157866201 | CTGGACCCTGTCTCA[A/G]GGATCCTCTTGAGGA | 51429 |
| rs559233128 | in-del | -/TT | 0.0148318 | 0.0848288 | intron-variant | SNX9 | GRCh38.p7 | 6:157901855 | ATTTTTATTTTGGTC[-/TT]TTTTTTTTTTTTAAC | 51429 |
| rs559248205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157736592 | ATATACAATCATGTC[A/G]TCTGCAAACAGAGAC | 51429 |
| rs559260041 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157742064 | TATAACACTATTTAT[C/T]TCCTCTCTCCAGCCT | 51429 |
| rs559265427 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157819655 | GTTGGGCTCTGAGCT[C/G]TTAAAAACCAAAGGA | 51429 |
| rs559268466 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157834365 | TTTTTTTTTTTTGTA[G/T]AGACGGGGTCTCAGT | 51429 |
| rs559269677 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157725074 | TCGATATCATAAGAT[A/T]CCTGGTTGACTTTTT | 51429 |
| rs559283743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157847239 | TCCAAGTTAGCTGAG[A/G]CCACAGGTGTGCACC | 51429 |
| rs559284402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157870745 | CTGTGCAAGCATGCA[C/T]ACCCCTCAGACACTC | 51429 |
| rs559285257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157764000 | CCCTTTCTGAAAACT[A/G]ACACACTATATCCAG | 51429 |
| rs559307330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157912638 | AAGAATTCCCCTCTC[A/G]CTCAACTACTGGAGA | 51429 |
| rs559320070 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157899647 | GGTGTGGTGGCAGGC[A/G]CCTGTAGTCCCAGCT | 51429 |
| rs559337915 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157745034 | AAGGGTGAGCCACCA[C/T]GCCTGGCCCTTTCTT | 51429 |
| rs559340039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157752887 | TCCCTGCGGCCTTCC[A/G]CAGTGTCTTGTGTCC | 51429 |
| rs559342812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157773863 | AGAGCAGGCTCCAGC[A/G]GAGGTGATGAGGTCG | 51429 |
| rs559352035 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157743590 | TATTGCAAACCTTTG[A/G]TTAATTTCCAGAGTT | 51429 |
| rs559356306 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157913211 | TGCTTTAGTACAATG[A/G]TGGTGTCTAGACTCA | 51429 |
| rs559374867 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157872722 | GGATTTCCACTTGAT[A/T]CTGTTGACCAGCGAG | 51429 |
| rs559398747 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157867360 | AACAGGGCTATCACC[G/T]TTGGTGTTATTCTTC | 51429 |
| rs559418816 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157846487 | CCTCATGTAACCTAG[A/T]TGTATATGTATTTAT | 51429 |
| rs559423094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157906283 | TACTTTAAAGCTAAG[C/T]GAGTTATTCATCTTT | 51429 |
| rs559429847 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157774526 | GGGAGGAAGGCCCTG[C/G]GGTCATCGACCCACG | 51429 |
| rs559446064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157934942 | AAGACTTAGATACCA[A/G]TTGGAAGAGCCTACC | 51429 |
| rs559448554 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157879030 | AAAGCTAGTGTCATA[C/T]AGGTGTGGTCAGACA | 51429 |
| rs559461296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157716983 | CCGTCTGTCATCTCC[A/G]CACTTGCTGGGCTGC | 51429 |
| rs559486057 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157868080 | TGTCTTAACTGATTG[A/T]TCCTATCATCATTTT | 51429 |
| rs559490610 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157840871 | AAAGTGAATACAAAC[A/G]GCTCATCAGACCATT | 51429 |
| rs559497163 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157877564 | AATTGGTAGCTTTTT[A/G]AACATTTTCCTATCA | 51429 |
| rs559504070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157757896 | CCTGAGAAATGTCCC[C/T]ACAGCTGGAGCGTAG | 51429 |
| rs559511798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157872082 | TTATTCAGATTCAGA[C/T]TATTAACTAATTAGG | 51429 |
| rs559549456 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157868770 | TCATTGCAGGCTTAT[A/G]TAGATGGAGAAGGAA | 51429 |
| rs559554195 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157770352 | GGCATTTCAATAACA[A/T]GAGCTTTGAGTTGGC | 51429 |
| rs559554455 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157804699 | ACTGATTTAAATGTT[A/T]ATCTCATTTAAAAAA | 51429 |
| rs559555035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157819039 | GATGGAGAAAGAAAT[A/G]TGACTTAGTCAAAAT | 51429 |
| rs559564023 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157804125 | TGGCCTCCCAAAGTG[C/G]TCATATTACAGGCGT | 51429 |
| rs559569804 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157905922 | TTCTGGAGTCAAACT[G/T]TTCTGTTTACCAGAT | 51429 |
| rs559583331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157899976 | AAATCTCCCTCAGCA[A/G]GTTTCCCAAATATAA | 51429 |
| rs559587497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157940719 | ACTGCGCCCAGCTCA[A/G]CTTGTTTTTCTAACC | 51429 |
| rs559607044 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157780833 | TGTGTAGCAACCTCT[C/T]AGGACGATGACATTT | 51429 |
| rs559607502 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157860485 | GCACAGGCAGTCACA[C/T]GTAGGTTTCAGAAGT | 51429 |
| rs559659826 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157745209 | ATCTCCCTGAGCCTC[G/T]GTCACACTCATCTAC | 51429 |
| rs559662143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157733136 | ATACTCTCCAAGTAC[A/G]TTGTTTTGAGCAATG | 51429 |
| rs559663621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157840377 | GAGGGTTTTCACCAC[A/G]CCCAAAATGACTGAC | 51429 |
| rs559678735 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157850398 | GGAATATGTGGGGTT[A/G]AGGGATGGTTTCTTC | 51429 |
| rs559679577 | in-del | -/T/TTTCTTTCTTTCTTTCT/TTTCTTTCTTTCTTTG/TTTT | 0.0111196 | 0.0737302 | intron-variant | SNX9 | GRCh38.p7 | 6:157780717 | TTTTCTGTTTCTTTC[lengthTooLong]TTTCTTTCTTTCTTT | 51429 |
| rs559695898 | in-del | -/TC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157876157 | TTTGCTTATAAAATA[-/TC]TGTTTATTAGCCAGG | 51429 |
| rs559706403 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157852440 | CCCTCCCTTCCTCCT[C/T]TCGCTACCATGGTCA | 51429 |
| rs559712083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157883496 | AGTTAGGCAAGCAGA[C/T]GCTGAACGGTTCATG | 51429 |
| rs559717174 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157899773 | AGCGAGGCTCCGTCT[A/C]AAAAAAAAAATTATC | 51429 |
| rs559733196 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157782794 | CGGGAGGCTGAGGCA[C/G]AGAACTACCTAAACC | 51429 |
| rs559742664 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157741598 | TGGCGGATATCTCAT[A/G]CAACAAGAAAATTCA | 51429 |
| rs559762530 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157748312 | AACATTGGATATCTA[C/T]GATAAATATTTCCTT | 51429 |
| rs559783563 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157919386 | TAATATTTTACGTTT[A/G]AGTTTTTTTTCTCTG | 51429 |
| rs559785458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157834641 | ATTACAGCCTCCCAA[A/G]CTGTTAGTGTCCACT | 51429 |
| rs559789900 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157719955 | GGAGAATCACTTGAA[C/T]CTGGCAGATGGAGGT | 51429 |
| rs559805639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157927926 | ACCAAAAGTATAGAC[A/G]AGTAACACACACACA | 51429 |
| rs559806769 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840033 | ACTGGGAAGGTGACA[C/T]TCAGGTAGAGATCTG | 51429 |
| rs559810662 | snp | A/G | | | intron-variant, downstream-variant-500B | SNX9, LOC105378078 | GRCh38.p7 | 6:157884919 | CCAGCATTGTTATAC[A/G]TACATCCTGTCATCA | 51429 |
| rs559811775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157791329 | ATACAATGGAAGTTA[C/T]TTTTCCTAATAGCAA | 51429 |
| rs559815779 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887703 | ATTGGGAGCATAAAC[A/T]GGGTCCCTGTTACTC | 51429 |
| rs559827927 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157745796 | CAGGCACAGTGTGTC[C/T]GTGGTCAGATGCCCA | 51429 |
| rs559836621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157739482 | TGGAGAAATAGGAAC[A/G]CTTTTACACTGTTGG | 51429 |
| rs559839934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894341 | TCTCAAACTCCTGAC[C/T]TCAGGTGATCCTCCC | 51429 |
| rs559852724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157842905 | CTGCAAAGGCAGACT[A/G]GACCCCAGACAAGAA | 51429 |
| rs559865905 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157778818 | CTGCACAGGCTCCTA[C/G]GTGGAAACAGGGAGC | 51429 |
| rs559870351 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157761693 | GCTGTTCTGAGCCTC[A/G]GTTTCTCCATTGGTA | 51429 |
| rs559874155 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157727632 | AGATGGGTCCTGGCA[C/T]GAGGAGTGTAAGGCT | 51429 |
| rs559891065 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157793354 | TCTGAAACCCAAGGA[C/T]CTTGGCTTTGGAGAC | 51429 |
| rs559896644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157878295 | TAGAATTGTCAGTGT[A/G]AAAGGAATATGATGA | 51429 |
| rs559902383 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157722544 | TGTCTGTGCCTCCAC[A/G]GCCATTTTGCTCCAG | 51429 |
| rs559903757 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894813 | TAAATACACAGTCTC[C/T]TTAAGCCTAGCATTT | 51429 |
| rs559905701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157739949 | ACCAGGGCCCTGTCG[A/G]GCGGTGGGAGCCTAG | 51429 |
| rs559908070 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157907526 | CCTGACCTTGTGATC[C/T]GCCCACATTGGCCTC | 51429 |
| rs559924380 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157862676 | TTTTTTTATTGCCAG[C/G]GTTTTGTGAATTTTT | 51429 |
| rs559951175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157739030 | ATACCATTCAGTACA[A/G]GCATGGGCAAGGACT | 51429 |
| rs559955554 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157779593 | CCTGGGTTGGAGTCT[C/T]ACCTCCACCACTTGA | 51429 |
| rs559960422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157897558 | CGTTGCCCAGGCTGG[A/G]GTGCAGTGGCACAAT | 51429 |
| rs559966288 | in-del | -/ACAC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157869972 | CACGTGTGCACTCTT[-/ACAC]ACACGTACCTTCTCA | 51429 |
| rs559972185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157884047 | TACAGATTTCCTGAA[C/T]CCCTGCCTTGGAGAA | 51429 |
| rs560008926 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157790016 | GTTCGCGTTCCAGCC[A/G]TCAGGACCACTTTCC | 51429 |
| rs560030362 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157833960 | GCAAGGAGACAGGAG[C/T]TGGACTTAAGTCTGT | 51429 |
| rs560035782 | snp | A/C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157747002 | AACCTAGATCCTTCA[A/C/T]ATGCACAGTTCCCGA | 51429 |
| rs560037132 | snp | C/T | | | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157944128 | AACACTGGCAGCCAC[C/T]GTCTCACCCCTGCGG | 51429 |
| rs560037877 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157877628 | GTAGGAAGATGTGTG[C/T]TCTGAGGTGAGCTGC | 51429 |
| rs560053947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157937305 | TTTAGAAAAAGTGAT[C/T]TGAATGCTTAACACT | 51429 |
| rs560065678 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157913492 | TTCTAAAGGAAAGTT[C/T]AGGTTTCATTTTTTA | 51429 |
| rs560088257 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157883003 | GAGAAATCTTTCATG[A/G]AAGGAAGAGTCAATT | 51429 |
| rs560098425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157910510 | ATGAAGGAAGAAGCT[A/G]CCAGGTTTTCTACTT | 51429 |
| rs560109022 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157898549 | GATGGGATGTGGCTC[A/C/G]TCCTGCTGGTTTAAG | 51429 |
| rs560109278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157904974 | ATGACTTAGTTGCCA[A/G]TGACTGAAATGTACT | 51429 |
| rs560114261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157843308 | TTAAAGTATAACTTT[C/T]GACTCCCCCAAAACT | 51429 |
| rs560124309 | in-del | -/AG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157791954 | TGGAACATTTAATTA[-/AG]GTGATCTGGAAACAC | 51429 |
| rs560130674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157794285 | ACTTTGCTCCTTCTT[C/T]GCCTTCTGCCATGAT | 51429 |
| rs560140614 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157741334 | TCTGGGTAACACAGC[A/G]AGACTCTGTCTCAAA | 51429 |
| rs560149861 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157786672 | TAAATTTTTAAATTT[C/T]ATTTAAAATCACAAT | 51429 |
| rs560158064 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157814402 | CATGCCATCCTTCCT[C/T]CTTGAAAACTGGAAA | 51429 |
| rs560171303 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157910606 | ATTACCCTCTCCCTT[C/T]TCTTGTTTTTTAAGT | 51429 |
| rs560178095 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157942559 | GGGAGCATGTGTAGA[C/T]GCCTCCCGGCGGGAA | 51429 |
| rs560181960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157760495 | AGTGGCCTCTATCTC[A/G]ATCAGTCTGGTGAGG | 51429 |
| rs560184820 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157837208 | TGTCAGTAACTTTTC[A/G]GTTCTTTTGATTGAT | 51429 |
| rs560200230 | in-del | -/AGTT | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157867868 | AAGTTCCCTAAAGAC[-/AGTT]ATGTATGTAATTGAG | 51429 |
| rs560215770 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157902210 | TAACTGAGAAGCTTA[C/G]TTAAAAAAAAAAAAG | 51429 |
| rs560222687 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157898049 | ATATCAGAACAAAAG[A/G]TACACCTTGCACACC | 51429 |
| rs560244898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157904544 | AATGCTTACAAGCTG[A/G]TCAAGGAGTTGTCAT | 51429 |
| rs560250691 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157943351 | TCATTGAGGGAAGTC[A/G]TTACGCCTTTCACTG | 51429 |
| rs560300845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157801082 | CTACCTTTCTTTGGG[C/T]GTATGACTTCAGGTG | 51429 |
| rs560304167 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157917472 | CATTCTATAAAGTCT[A/C/G]CCTTATTGAGTTTTC | 51429 |
| rs560338992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157925625 | ATATTATACAGCAAT[A/G]AAATGAATGAACTGT | 51429 |
| rs560340393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157870879 | ATGCAGCACTCACCC[A/G]TGCAAGCACGCACAC | 51429 |
| rs560360310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157767791 | TAGAAAATTGTTTAA[A/G]AAGTGACATGTTGAA | 51429 |
| rs560371644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157899008 | TTCTCCATAATGGCA[C/T]TCTTAGGACCTGACA | 51429 |
| rs560376809 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157901193 | GCACTGTCTTTACAC[A/G]ATCCTGCATGCAATT | 51429 |
| rs560377477 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157769532 | AGTAAGCGTCAGCCA[A/G]GGGAAGACAGAGAGG | 51429 |
| rs560420301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157787107 | TCAGTTGAAGGTCTT[A/G]CTAGAAAAAAAAGGC | 51429 |
| rs560432797 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157881176 | GGTGTCTCTGTTTCA[C/T]GTTTTGTTAATTCTT | 51429 |
| rs560436737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157741833 | AATAAGACTCTTGCT[A/G]AAATTACTAAAGCAT | 51429 |
| rs560462249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157924275 | AAAATCCCAGAGGTA[A/G]AATGGAGGAGAATAC | 51429 |
| rs560477597 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157924878 | TTGAAAGTTTTCATT[G/T]TATATGGTCTTCTTG | 51429 |
| rs560480560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157723290 | GACCTACTTTCTACA[C/T]ACTTTAGTATTTTAA | 51429 |
| rs560484031 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157858707 | AGATTTAATGGACTC[A/G]CAATTCCACATGGCT | 51429 |
| rs560501398 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157768370 | CAGCAGCAGTCAACA[C/G]CACCCTGGGGCTCAG | 51429 |
| rs560506399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157851519 | ACTCCCTGTAGCCCC[C/T]GGTAACCCCCATTCT | 51429 |
| rs560515719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157810107 | TTGTGGCATATCCAT[C/T]GAACAAAATACTACT | 51429 |
| rs560524426 | in-del | -/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157799849 | GGAATTCTGGGAGAT[-/C]CAATTCAAGTTGAGA | 51429 |
| rs560544543 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157918038 | TTATGGCCTAGCATA[C/T]GGTCTGTCATAGGGA | 51429 |
| rs560556352 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157715644 | TCTGTGTGTGTTTTT[A/G]TTATTCTCTTTTATA | 51429 |
| rs560579435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157892426 | AGGGTTTTGAGAAAT[A/G]TGTTATCAGCAGGAG | 51429 |
| rs560606348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157911054 | GGAGGCAGAGGTTGC[A/G]GTGAGCCGAGATTGC | 51429 |
| rs560611280 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157762777 | CGAGTCTCTAGGGGG[C/T]AGCAACTTGGGGAGA | 51429 |
| rs560618872 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157730546 | AACAAAAACAAAAAC[A/C]AAAAAGTAGATAAGT | 51429 |
| rs560642969 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157833995 | CCACGCTGGGGGCTA[C/T]GTCAGGTTTTGTACT | 51429 |
| rs560656576 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | SNX9 | GRCh38.p7 | 6:157716191 | TTCCTCAGGCATTTT[G/T]TCCTGGACACAGGTA | 51429 |
| rs560661164 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157842459 | CGATTTATCAAGACA[A/G]GGGGATTGCAATGGA | 51429 |
| rs560684646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157750645 | TTCTGCACAGCAAAG[A/G]AAATAATCAACAGAG | 51429 |
| rs560685641 | in-del | -/AATG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157910494 | GAACTACTAAGTGTT[-/AATG]AAGGAAGAAGCTGCC | 51429 |
| rs560696193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157844795 | AGACAGCATTTCACC[A/G]TGTTGGTCAGGCTGG | 51429 |
| rs560711907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157935519 | ACCCCACGAAAAGAA[A/G]GGTGCAGGGAAAAAA | 51429 |
| rs560746826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157799386 | TAAATCAATTACTCT[C/T]ACCCAGTGGGTCTCC | 51429 |
| rs560781553 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157772903 | AGATCATGGGGGAAT[A/T]AGGGGTGAGCTGGAG | 51429 |
| rs560815385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157901255 | TTTTATTCCATAGCA[A/G]TAGTTTCAGGGGGTC | 51429 |
| rs560830194 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157726590 | ATTCTTATAAATATT[C/G]TTGGACAAATTAAGT | 51429 |
| rs560836482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157862419 | GTTATACATAGAAAT[A/G]TTACCTACTCTTTAT | 51429 |
| rs560859097 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, nc-transcript-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157892964 | GTGGCCCTCCGAGCC[C/T]CTCCATTTCACAGCC | 51429 |
| rs560859350 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157795839 | TACAATTTCAATGTT[A/G]GAACAGCGTCTGGGG | 51429 |
| rs560861632 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157798765 | ATGTGAATGCACTTA[A/G]TGCCACTCAATTGTA | 51429 |
| rs560861684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157806103 | ATTAATAAAAGTACG[A/G]TTATATCTTTCATCA | 51429 |
| rs560901164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157863256 | CATACTCCTCTCTTT[C/T]CTCAGAAGAGGAGGT | 51429 |
| rs560924253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157828004 | TAAGACTTGTTTATT[C/T]CATGCATAGATTAGT | 51429 |
| rs560931673 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157841596 | CCAGTGAAGTAGGCT[G/T]TGTGTAGCTTTCCCA | 51429 |
| rs560944826 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157752831 | TCAGACTATCACATG[A/G]GGAGAAACCTTGGAC | 51429 |
| rs560973824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157940838 | CAGGTGTTGTCATTT[A/G]AAAACTTGAGGGAAA | 51429 |
| rs560980975 | in-del | -/CCAGCAGTCACCAATCGCT | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157805247 | TGACTCATTGGTGTC[-/CCAGCAGTCACCAATCGCT]CCATCTCCCGTGTCT | 51429 |
| rs561000120 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157739355 | TGAAAAAAAGCTCAT[A/C]ATCACTGGTCATTAG | 51429 |
| rs561002810 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157718235 | TTGTGAATACTGCTA[C/T]AGCTGACAGTCCAGG | 51429 |
| rs561026326 | in-del | -/A/AA/AAAA | 0.40595 | 0.195396 | intron-variant | SNX9 | GRCh38.p7 | 6:157721280 | GCGAGACCCCACCTC[-/A/AA/AAAA]AAAAAAAAAAAAAAT | 51429 |
| rs561047409 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157819363 | AAGGTGAGGACGTCA[C/T]ACGTTTATTAGGATT | 51429 |
| rs561055187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157896101 | TGCTCGTTCTAGATT[A/G]TAGGAAGGAGGCTGC | 51429 |
| rs561064915 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157913807 | CACATTTGCAATTCA[A/G]TCATTTTGTTGTGTC | 51429 |
| rs561082353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157753840 | TAATATACGCAGAGC[C/T]GGCTGTATGGGAGAC | 51429 |
| rs561110552 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157729019 | TGAGGCAGGAGAATC[A/G]TTTGAACCCAGGAGG | 51429 |
| rs561116749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157856465 | AAGATGGGGAGGAAA[A/G]AGGAAAGTCTTTTAA | 51429 |
| rs561131822 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157908834 | CCAGTGAGCTAGTGT[-/A]AGCCTCGCCTGAATT | 51429 |
| rs561134649 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157915514 | TTTCAGGCCAGGCGC[A/G]GTGGCTCATGCCTGT | 51429 |
| rs561144996 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157915106 | AAAAATCAGTTGATT[A/G]TATTTGTTGGTTTAT | 51429 |
| rs561154778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157759334 | AGCTGGCCCTGATGG[A/G]CCCAGGAGCACTCAT | 51429 |
| rs561175700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157746504 | TTTCTGTCCTTAAAC[A/G]TTAAGTATCAAGGGG | 51429 |
| rs561178158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157857330 | CATCTTGTATGTTTT[A/G]TATGGGATTCTTGTT | 51429 |
| rs561191643 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157753048 | GCGAGCACAGGGTTG[C/G]GGGTAGGGTTACAGA | 51429 |
| rs561195803 | in-del | -/T | 0.0183727 | 0.094068 | intron-variant | SNX9 | GRCh38.p7 | 6:157901856 | TTTTATTTTGGTCTT[-/T]TTTTTTTTTTTTAAC | 51429 |
| rs561205327 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157843839 | CATCGTGAGTACAGA[A/G]TTCTAGATTTTAAAA | 51429 |
| rs561218180 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157776702 | TGGGGTGGCCCCAGG[C/T]CCCATGGGCCTCTTA | 51429 |
| rs561231467 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157847395 | GTTGTGAGCCACTGC[A/G]CCCAGCCTTGTAGTA | 51429 |
| rs561233823 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157734701 | AGAAATACTCTTGAA[A/C]AAAGGCCTCTCCAGC | 51429 |
| rs561240840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157784783 | TTAAAAATCTGAATA[C/T]CTTTATATCTACCAA | 51429 |
| rs561248673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157875958 | CAAGCCTGGGCAACA[C/T]GATGAAACCCCATCT | 51429 |
| rs561263602 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157740217 | TTTGTGCAAGGCCAC[A/G]TTGCCCAACTCCAAG | 51429 |
| rs561288029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157766163 | ACCTACTGAGTCCTC[C/T]GTCCACTCACAATGA | 51429 |
| rs561323788 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157760162 | AGGCGTGAGCCACCA[C/T]GCCCGGGCCATCAAG | 51429 |
| rs561324069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157882375 | ATGGAGATGTACATG[A/G]AGATTGATGTTTTCA | 51429 |
| rs561352138 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157945564 | ACCCCCCATCCCCCC[A/G]CCCCCGGTGGGCAGC | 51429 |
| rs561357899 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157942374 | GGCTCGTGCTGTCTG[C/G]ACACTCAGCAGTGAC | 51429 |
| rs561367729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157832004 | GCTGTCAAACTGTGG[A/G]CATTTCAAAACTTTC | 51429 |
| rs561377362 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157756924 | TGCAGAGAGGACGCC[A/G]GGAGAATCCAGCTAA | 51429 |
| rs561383027 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157804508 | GCAATCAGTAGTAGA[A/G]AGAGAGAGAGGAAGT | 51429 |
| rs561388955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157882756 | TTCTTCAACCTCATG[A/G]TAAAACTTGAACAGA | 51429 |
| rs561392244 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157805308 | CCTGGGGCCGCCATC[C/G]TGACCCAGGTTCTCA | 51429 |
| rs561436008 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157932673 | GAGTTTGAGACCAGC[C/T]TGGGCAACATGGTGA | 51429 |
| rs561437266 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157923973 | CAGGCTGGGTGTGGC[A/G]GATCACTTGAGGTCA | 51429 |
| rs561442328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157838236 | CAGGCTGGTCTTGAA[C/T]TCCTGGGCTCAAGCA | 51429 |
| rs561451699 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157807291 | TGATCCCCAAGTCAT[G/T]AGTCACTTTCTTCTA | 51429 |
| rs561472223 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157747129 | GCTATGCAGCCTGGT[C/G/T]CCTAACAGGCCATGG | 51429 |
| rs561473343 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157875599 | TCTCAGAGCTAGAGG[-/C]CCCTCATCCTGCGAG | 51429 |
| rs561478093 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157831315 | CCAGGGAGGATTTGT[A/G]TGTGCTGATACCAGT | 51429 |
| rs561478714 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157935405 | GGTCTAATAGCCAGT[C/G]TGAAGAGAACACAGG | 51429 |
| rs561480118 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157839126 | ACAGGTTTACTTAAA[A/T]ACGCTGGACTTCATA | 51429 |
| rs561494630 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157936796 | TTATTGGAGTCTTTA[C/G]TACCCCAGTTTCAGG | 51429 |
| rs561501284 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157864509 | TAAACAAGAGGCTTA[A/G]GTATTCTATATTTGG | 51429 |
| rs561509955 | in-del | -/TTTTTTTTTTTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157834174 | TTTTTTTTTTTTTTT[-/TTTTTTTTTTTT]GAGTCAGGGTCTCTC | 51429 |
| rs561510411 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157731777 | CATTCCCCTCTCAAA[G/T]ACCCTCTTACTCTGT | 51429 |
| rs561516546 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157859636 | AATAGTACAACCCCA[A/G]ATTGTGGCCGTGGGG | 51429 |
| rs561590326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, nc-transcript-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157892915 | AAGAGAGGTAGAGCT[A/G]TTAACGGAATTCCAA | 51429 |
| rs561604852 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157916057 | TTTTTTTGTTTGAGA[C/T]GGAGTCTCGCTCTGT | 51429 |
| rs561607236 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157806806 | ATATATATTTGGCTT[C/T]AGCCCTGGAAAAGCC | 51429 |
| rs561608285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157844743 | GGACTATAGGCACCC[A/G]CCACCACGCCCGGCT | 51429 |
| rs561610147 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157902162 | GTGATCTCCTAAGTT[A/T]TGGATATGATTCAGT | 51429 |
| rs561615390 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157784238 | CAAATTTGATTCTTT[C/G]AAAAGGTTAATCAAA | 51429 |
| rs561618431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157924993 | ATCCTAGAGAGCAGG[A/G]AAGAATTTCTGAAAT | 51429 |
| rs561626056 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157788735 | TTTTCTGTAAATTAA[C/G]TTGTATGTTAAATGC | 51429 |
| rs561650254 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157731238 | GACCTCGTGATCCAC[G/T]TGCCTCGCTCCTGAA | 51429 |
| rs561666106 | in-del | -/TAA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157740113 | TAATAATAATAATAA[-/TAA]ATCTTTATTTAACCA | 51429 |
| rs561669441 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157786107 | GAGTGCGGTGGCACA[A/G]TCATAGCTCACTGTA | 51429 |
| rs561671405 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822755 | CCGCAACACCCCAGG[C/G]GTGGGGCAAAGACAG | 51429 |
| rs561677236 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157925532 | AGACATCTACATAAC[A/C]GCTTCATTCATAACT | 51429 |
| rs561702315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157853514 | AATTTTTGACATTAC[C/T]TCTTCAGACACTTTT | 51429 |
| rs561704793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157866966 | TGTTTGTTTTTTTAA[A/G]AGACTGCAGGGTCTC | 51429 |
| rs561743159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886692 | TTATGTCGAATTCCA[A/G]TTTGGAATTCAGGAT | 51429 |
| rs561767166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157765929 | GTTGTCTGGGAGCAC[A/G]TTTCCCCACCAAATT | 51429 |
| rs561815756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157918983 | TTTGTCTTTTAAAGA[C/T]ACTAAGGAAACAAAT | 51429 |
| rs561818095 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157872485 | GAGCTGCACTGCGTG[A/T]GTCTGCAATCACTGG | 51429 |
| rs561833225 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157774399 | TGAGTGGGTTCCACA[C/G]TGGTGGGAGGAAGCC | 51429 |
| rs561837628 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157820165 | GACAAACGCCACCAC[C/T]GGGTGCAGTGGCTCA | 51429 |
| rs561848658 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157795190 | GGAGGCCAAGGCGGG[C/T]GGATTGCTTGAGGTC | 51429 |
| rs561857810 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157742333 | AAGGAAAGGCAGAAG[C/T]AGCTGTGTTTGACTC | 51429 |
| rs561869402 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157905759 | CAGCATGTGGCTATT[G/T]CCCCCTGTGGCCAAC | 51429 |
| rs561878115 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157942180 | TATGGCAAAGTAACC[C/T]TTAAGTTACTAAAAT | 51429 |
| rs561886761 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157724335 | AAGTGAAGCAAAATA[G/T]CTTGGAACAGTCTGA | 51429 |
| rs561899696 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157782578 | TATTTTTATAAATGT[A/T]AAGAAGATTTTATGT | 51429 |
| rs561901760 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157944430 | TACAAATTGTAAAGA[A/G]TATGTATAAATGTTT | 51429 |
| rs561923264 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157895731 | TGAGTAAGTATATAC[A/G]AGGAATTTGTTAGTA | 51429 |
| rs561945009 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157792171 | TTTTTTGATACAGAG[A/T]CTCACTCTGTTGCCA | 51429 |
| rs561948948 | in-del | -/TTAC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157857544 | TTTTCCTTCAGATAG[-/TTAC]TTATTTGTTCTAAAA | 51429 |
| rs561955024 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157944645 | ATCCTATTTCTTCTG[A/G]CATGAATTCATCATT | 51429 |
| rs561957393 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157846349 | TAGTTCTGTGGTGAG[A/G]TTTATGTTAGCTCTG | 51429 |
| rs561972758 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157798025 | CAGCAAACACCAGTG[C/G]ATAATAAAACTAGTG | 51429 |
| rs562008635 | snp | A/C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157728929 | ACATGGCGAAACCCC[A/C/G]TGTCTACTAAAAATA | 51429 |
| rs562016999 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157722958 | CAGTGAGTCAAGATC[A/G]TGCCACTGCACTCCA | 51429 |
| rs562023364 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157933378 | ATAGAAGTGGTAGAA[C/T]TGGTACAGGTGTTGA | 51429 |
| rs562059054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157804499 | TAAACACAGGCAATC[A/G]GTAGTAGAAAGAGAG | 51429 |
| rs562060442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157818323 | TTTCACGTTTTTCTG[C/T]CTGCTTTATATTCTA | 51429 |
| rs562060467 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157917955 | TTTCTTTTGACCTCC[-/A]GTTTTATTATGTTCA | 51429 |
| rs562068359 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157880447 | GAATTTTCTCTTTGA[A/T]TTGCCCAATTTCTAG | 51429 |
| rs562091400 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157933992 | AGTTCCTGTTGACTG[A/G]CTTTTCTCCCATTAC | 51429 |
| rs562100302 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157939913 | ATAGGAGGCATCCGA[A/G]GGAGGCAATGAGGTC | 51429 |
| rs562111385 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157854859 | CTTTCATAAATTTTG[A/C]TGTTTGCAACATGAC | 51429 |
| rs562138303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157811772 | GTATTTAACACAAAG[A/G]TATATTGATGATCTA | 51429 |
| rs562156341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157760451 | CCAAAGGTTCAAATC[A/G]CAAAGTAGGGAGCTC | 51429 |
| rs562174985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157803951 | TGCAATCTCTGCCTC[C/T]TAGGTTCAAGCCATT | 51429 |
| rs562181460 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157720526 | CAGCAATGGCCTGGG[A/G]CCCAGCTGGGCTCAT | 51429 |
| rs562186044 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157756632 | TTCTTGCTCCTTGAA[A/G]GTGGACTTTGAGGAC | 51429 |
| rs562193840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157874304 | CCCCTGGCCTCACTC[C/T]GTAGGTCTTATGTTG | 51429 |
| rs562210880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157939458 | TCAAGGGAGAAGGAT[C/T]TGCTGGTTATGGAGG | 51429 |
| rs562218709 | in-del | -/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157834101 | CATGGGGTGACACCA[-/G]GGCTTGATCTGATCG | 51429 |
| rs562225898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157765975 | CTTTTAAAAACAGCT[C/T]ATTGTCATCAAGACA | 51429 |
| rs562230536 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157930496 | TACATGGACCATTAC[C/T]GCACAGCAGGAGGCA | 51429 |
| rs562287864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157834599 | GGCTCAAACGATCCT[C/T]CTGTGTCAGCCTCCC | 51429 |
| rs562292202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157738902 | GCTAGCCATATGCAG[A/G]AAACTGAAACTGGAC | 51429 |
| rs562297924 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157786204 | CTTGCCACTACATCT[A/G]GCTAAATTTTTTTTA | 51429 |
| rs562336621 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157904798 | TGCTCCCAAAACTCC[A/T]CCAGGTCCTGAAAAC | 51429 |
| rs562338689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157800331 | CACATGAAATACTTT[A/G]AAAGAATTATTTTAA | 51429 |
| rs562358425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157744600 | AGCCCTCTCACACCA[C/T]GGAAGATGCATCTCC | 51429 |
| rs562374390 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157786925 | GCTTCCCATGAAACA[A/T]CATGACCTATCCCCA | 51429 |
| rs562377251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157792770 | TATTAAGAGCCCTTC[A/G]ATGCTCAGTGTTTTA | 51429 |
| rs562384070 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157747322 | ACACAAGATATTTTC[A/G]CTGAATGAAAACAGT | 51429 |
| rs562386464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157777857 | GCTCTCAGCAGTCAG[A/G]TTTATTCACAGGCTT | 51429 |
| rs562404975 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157883086 | CCTTCAGCAACCACC[A/G]CCCTGATCAGTCAGC | 51429 |
| rs562408398 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157853537 | CACTTTTTCTGTCTT[-/C]CCCCTCCATCATTCT | 51429 |
| rs562419242 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157728047 | TCAGCTATTTATGCA[G/T]CCTTGGTCGATGGCT | 51429 |
| rs562429442 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SNX9 | GRCh38.p7 | 6:157916170 | CTCCCGAGTAGCTGG[A/G]ACTACAGGCACCCGC | 51429 |
| rs562436752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157856392 | CTCCTGCATTATTTT[C/T]GAAGAAATGGCAGGT | 51429 |
| rs562454549 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157927465 | TTGACACGGTGCTGA[A/G]TAGCTGTTTCCAATA | 51429 |
| rs562460241 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157730054 | AGCTAAGGGGTGCAT[A/G]CAGGGGTTCCTTTTT | 51429 |
| rs562460317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157785805 | CACCTGCTACTAAAG[A/G]GAATGTAATTGACCA | 51429 |
| rs562463779 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157807725 | CCCACATGAGGCAAA[C/G]AGCTGGAACTAAGAC | 51429 |
| rs562470020 | snp | A/G | 0.000692715 | 0.0185978 | missense | SNX9 | GRCh38.p7 | 6:157896840 | AGGTTGGCAGTGGCA[A/G]TGACCCCTGGTCAGC | 51429 |
| rs562494385 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157923446 | AAAAAAAATAACCTG[G/T]CATTTACAGTAACAT | 51429 |
| rs562516003 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157899631 | GAAAAAAAATTAGCC[A/G]GGTGTGGTGGCAGGC | 51429 |
| rs562520949 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157849470 | AGTCAAGAGCGGCAA[C/T]GCTTAGTGTGCATGT | 51429 |
| rs562538855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157806359 | TCAAACCCTCCAAAA[C/T]ATTTGATCATTGTGG | 51429 |
| rs562553019 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840190 | GAAAGAGCAGACCCT[C/G]AGGCTGGTGCTTGGG | 51429 |
| rs562561571 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157829933 | TTGTGGAAGGTTTGT[C/G]TTATAAGTCTCTTTT | 51429 |
| rs562579444 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157807175 | CACACTCTTCCTGCA[C/G]AGTTATAGGACAAGG | 51429 |
| rs562589287 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157869989 | ACACACGTACCTTCT[C/T]ACTCTCACCTCTCAT | 51429 |
| rs562669338 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157863696 | CCTCTGTCTGTTTGG[A/G]TACTGTTAGTGGTAG | 51429 |
| rs562683410 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157865655 | TCCACCATCTAGATT[C/T]AGTACCTGCTTTGTC | 51429 |
| rs562686097 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157816080 | CATGAGAGGAACCCC[G/T]GCCTCCTAAACTCCT | 51429 |
| rs562695613 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157837242 | TGGTATTATATGCAA[A/T]ATGTCTCAACACTGT | 51429 |
| rs562697549 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157715471 | GATTGCTTGAGCTGG[A/G]GAGATTGAGGCTATA | 51429 |
| rs562722664 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157924160 | CAAGATCATGCCACT[G/T]CACTCCAGCCTGGGC | 51429 |
| rs562742084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157903497 | GTCAACTGTGTCTTG[C/T]TTCAGAGTCAAATTT | 51429 |
| rs562768229 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157836328 | TGCTACAAGTATTAA[A/T]TTTTTTTCTCAAACT | 51429 |
| rs562780311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157942701 | TGGAATTTGTGTCAT[A/G]TTTAACTTGTTGGAG | 51429 |
| rs562781117 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157748871 | ATATGTTTCATTATA[A/T]TATCAACATCCTAAG | 51429 |
| rs562799783 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822891 | CGTGAACCGGAGTCG[C/G]GGTTCGGCTACCCCG | 51429 |
| rs562805056 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885452 | GAGCTAAAGTGGTTA[G/T]ATTTTTTTATATAAG | 51429 |
| rs562816236 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157815629 | TAGCACTTTGCACAT[G/T]GTAGGCTCTCAATAG | 51429 |
| rs562816709 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157817554 | CATGTTATGTGGGGC[A/T]TTTAGCTTTAAAAGT | 51429 |
| rs562820099 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157793232 | TCGGATTACAGGCGT[G/T]AGCCCACGCACCCAG | 51429 |
| rs562836407 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157747768 | TACTAATCCCATATA[A/C]AGTATATTTATGGAA | 51429 |
| rs562839219 | in-del | -/CCTGTAAGACCACCTGG | 0.0471551 | 0.14613 | intron-variant | SNX9 | GRCh38.p7 | 6:157724005 | AGTTGGGGGCTCGGC[-/CCTGTAAGACCACCTGG]CCTGTAAGACCACCT | 51429 |
| rs562844154 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157775146 | TGGATCACCTGAGGT[C/G]AAGAGTTTGAGACCA | 51429 |
| rs562850105 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157810020 | TATGCAATGTTCATA[G/T]TAACATTATTCACTA | 51429 |
| rs562858995 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157772636 | TTCAGAACTGGGGGA[G/T]AATACATTTCTGCTG | 51429 |
| rs562895321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157843699 | AGACAGACAGCTATG[A/G]TCTTTGTGTACTTCT | 51429 |
| rs562907909 | in-del | -/ATT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157836230 | GCTGGGATTATAGCC[-/ATT]ACCCTTTTTGATAAG | 51429 |
| rs562922941 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157869998 | CCTTCTCACTCTCAC[-/CT]CTCATGCACACCCAC | 51429 |
| rs562929292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157819695 | TTTGAATAAAAACAC[C/T]TGGCCATACTGAACA | 51429 |
| rs562961104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157830350 | GCATTTTCTCCTAGT[A/G]CAATGAAGGTATTCT | 51429 |
| rs562979815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157864604 | ACAGCAGGTTCCTCA[C/T]GCCCGTGAGTGTGGC | 51429 |
| rs562997261 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157828812 | TAAGCATCACTTCCC[C/T]GGGAAAGCCTTTCCT | 51429 |
| rs563003230 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157870392 | GTGAGTGCATGTACC[C/G]CTCAGACACTGTCAC | 51429 |
| rs563009934 | in-del | -/T | 0.00597247 | 0.0543191 | intron-variant | SNX9 | GRCh38.p7 | 6:157737511 | ATATCCCCTTTATCA[-/T]TTTTTTTTGCGTCTA | 51429 |
| rs563022716 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157912721 | TAATTCATGAAAAAA[C/T]GTACAGTTAACATTT | 51429 |
| rs563023822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157930624 | AGAAATTTGCACCCT[A/G]TTAAGAGCCACGCAT | 51429 |
| rs563024411 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157768139 | CTCTGACCCTTCGGT[C/G]TCACCATCCACGCTA | 51429 |
| rs563032544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157850614 | CCACTTTCTGAAGTT[A/G]GGGTAAAGGTCATGG | 51429 |
| rs563040797 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157753283 | GTGAATAGAGATTAT[A/G]GATAATTATGGATTC | 51429 |
| rs563044484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157755981 | ACCCACCCATCAAGT[A/G]TGTCCTTTGAGGTGA | 51429 |
| rs563047834 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157823700 | GGGTTGGGACCCCGG[G/T]CGCAGCGAGGTTTGG | 51429 |
| rs563065277 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157782519 | ATTGTAATCACTACA[C/G]TAACTACTAAAAAAC | 51429 |
| rs563082439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157723173 | ACTTCATAATCTGTC[C/T]AACCACCCTTATGTC | 51429 |
| rs563084980 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157756406 | GCTGGGCAACAGAGT[A/C/G]AGACTCTGTCTAAAA | 51429 |
| rs563091159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157819116 | CATAATTTTAAAACC[A/G]TACACTTTTCATACA | 51429 |
| rs563109598 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157940805 | GGTTGATGATTAATT[G/T]TAACTGAGCAGAGAA | 51429 |
| rs563114361 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157844198 | TTCTTAGAGCCGATT[G/T]CTCAGGACAAGCGGA | 51429 |
| rs563160696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157761438 | GAGCATTCTTAAAGA[C/T]GCAATTTGTGTTTTG | 51429 |
| rs563166851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157858521 | GCCACCATGCCCGGC[C/T]ATTGTCCAGAGTCTT | 51429 |
| rs563177497 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157722037 | GAATCCATAGCACTT[A/T]CCCATGAAGCCCGTT | 51429 |
| rs563203594 | in-del | -/GCCCTCAGCATGATT | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893196 | AAGTGTGACTGCCAG[-/GCCCTCAGCATGATT]GCCTTCATTTCCAGC | 51429 |
| rs563213031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157812656 | CCAGTGAAGGCCCCT[A/G]AAGACTTTGGGGAAG | 51429 |
| rs563215312 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157933660 | CTGAGAGCAAGCCAC[A/G]CCCATTGCTTAGGGA | 51429 |
| rs563222756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157898497 | CTCAGCAGCTAACAC[A/G]TTTGTTTTAAAATCT | 51429 |
| rs563225634 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | SNX9, LOC107986663 | GRCh38.p7 | 6:157714657 | TCACAATGTCTGCCA[C/T]GTGCAGAGGAGAGAA | 51429 |
| rs563243242 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157940190 | GCTGTGCAGGAGGGA[A/G]CGGGGCAGGGACCCC | 51429 |
| rs563263445 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SNX9 | GRCh38.p7 | 6:157725095 | TTGACTTTTTTTTCC[C/T]GATACTTCAGATGTT | 51429 |
| rs563291049 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157854486 | AGAGTATGTAAGCAT[A/G]TACTGTGATTCTAAT | 51429 |
| rs563294614 | in-del | -/TCTC | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157779589 | GGGCCTGGGTTGGAG[-/TCTC]TCTCACCTCCACCAC | 51429 |
| rs563302748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157861692 | TATGTTCCGAGACCT[C/T]CAGGGATGCCTGCAA | 51429 |
| rs563317385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157770514 | ATTTATTGGCCGGGT[A/G]CGGTGGCTCACGCTT | 51429 |
| rs563318074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157805301 | CTCTATCCCTGGGGC[C/T]GCCATCCTGACCCAG | 51429 |
| rs563324410 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157824203 | TGCTTGTTTTACGTT[A/G]TTGTTTATGAAATTA | 51429 |
| rs563331241 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157738324 | AACCTGGGTGCTCCT[A/G]TATTGGGTGCATATA | 51429 |
| rs563336847 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157945294 | ATTTTCTTATTGGTG[A/T]CTTTATTCACTTTCT | 51429 |
| rs563352966 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157847341 | CTCCTGAGCTCAAGC[A/G]ATCTGCCCACCTCCA | 51429 |
| rs563355514 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157826265 | GCACTTTGGGAGGCC[C/G]AGGCGGGCGGATCAC | 51429 |
| rs563359979 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157838716 | TGAAGGCATGTTTAG[A/T]TTGAGGTCTCATTTA | 51429 |
| rs563362773 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157739607 | TACTGGGTGTATACC[C/T]AAAGGATTATAAATC | 51429 |
| rs563364575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157835362 | TAGAGTTCAATTACT[A/G]TATAATGACCAAAAG | 51429 |
| rs563409733 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157907469 | TTTGTATTTTATAGT[A/T]GAGACGGGGTTTCAC | 51429 |
| rs563432859 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157935451 | GACATATCACCAGAG[A/G]CACAGCCAGCAGCAT | 51429 |
| rs563433659 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157753419 | AACTCAAAAAGGTAC[-/T]TCCATTTCTTCAAGG | 51429 |
| rs563438978 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157840951 | AGCAAAGTACTTGCA[C/G]ACTGCTGGATTTCTG | 51429 |
| rs563446525 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157807884 | CAGTGAAATACTGAA[G/T]TTCCAAACCTGCATT | 51429 |
| rs563476991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157841479 | TACCTAGAGACCCAT[A/G]GGCCTTCATGGGGTC | 51429 |
| rs563477065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157834890 | CAATGTCCTTGCAAC[C/T]CCTAAAAGCTCCAAA | 51429 |
| rs563492675 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157798167 | TAATCAAGTGATCAA[A/C]GTTAATATCATCTGT | 51429 |
| rs563508463 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157752467 | GGGGAGAGGGTCAGC[A/C]GGAAAACATGTGGAC | 51429 |
| rs563511403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157882322 | CTTTCAAAATATTAC[C/T]GCTCATTGACAATGC | 51429 |
| rs563524232 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157778128 | CTCTCAGGGGGCGCT[A/T]CGGGAGGGTCCCTTC | 51429 |
| rs563525015 | in-del | -/GTTAG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157917206 | TGTACCTTTAAAGAT[-/GTTAG]GTCTACTCCTTCATT | 51429 |
| rs563540674 | in-del | -/C | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822627 | GGCTTCAAGCCAGGA[-/C]CCCGGCCTGAGGGAG | 51429 |
| rs563549328 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157820910 | TCGATCTCTTCACCT[A/C]GTGACCCGCCCGCCG | 51429 |
| rs563562934 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157862302 | CTTCTGATGATCTTA[A/T]TAAGTCAAGATAAGA | 51429 |
| rs563566423 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157811386 | TATGCTAGAGCCACA[A/G]TTAGGGATCACCCCA | 51429 |
| rs563572050 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157750952 | TGACTGTTATTTTTT[A/T]AAAAATATAATAAGT | 51429 |
| rs563572148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157874991 | TTCTTGCTTGCCCTC[A/G]AAGACTCCCTGAAGT | 51429 |
| rs563584691 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157772311 | AATGCCCAGTACCTG[G/T]GACCTTATTTGAAAA | 51429 |
| rs563585164 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157765512 | AGGCGCCCGCCACCA[C/T]GCCTGGCTAATTTTT | 51429 |
| rs563587429 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157815665 | TTAGGCGTGAAATAA[A/G]AAGCAGCTAATACAC | 51429 |
| rs563598771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157798649 | GATATCATAGCAGCA[A/G]TTTACTCTTAAGTGG | 51429 |
| rs563611991 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894368 | TCCCGCCTCGGCCTC[C/T]GAAAGTGGTAGGATT | 51429 |
| rs563622225 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157748107 | ATTCTGTTAAATACA[A/G]AACAACATCATCCAT | 51429 |
| rs563626592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157752952 | TTAACAAGCATGCTG[C/T]CTTGAAGCATTTGTT | 51429 |
| rs563643965 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157868870 | TCACCTGGCTGATTT[C/T]GTGACACTGCCCTGT | 51429 |
| rs563645219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157726280 | ATTAATCCCATCCAA[C/T]GTATTTTTCATCTCA | 51429 |
| rs563655621 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157920735 | ATAGCTGGAACTTCT[A/T]CCACTAGAAGGCTTT | 51429 |
| rs563668036 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157783860 | ATCTTGGCCAGGCTG[C/G]TGTTGAACTCCTGAC | 51429 |
| rs563674159 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157873792 | TTCCCATAGACAGAG[A/G]GGTGTCTTGGGGGAG | 51429 |
| rs563690279 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157771465 | TGGATGTAATATCTA[C/G]TTTACATTTATAATA | 51429 |
| rs563693873 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157895308 | AGTCAGAGTTGTCTT[C/G]GTCTGGGTTGTAAAT | 51429 |
| rs563701321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157844072 | TAGAGACAGGGTTTC[A/G]CCACTTTGGCCTGGC | 51429 |
| rs563715168 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157717385 | CATTCCTGCTCCTTT[A/G]AGTGAAAGAAGCTTG | 51429 |
| rs563722475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157746464 | GGTAATGATCCTGCG[C/T]TTCCATCGCCAGGCA | 51429 |
| rs563723504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888556 | TTGTTCACTGGGCAC[C/G]TTTTTTATTTTAAGG | 51429 |
| rs563740950 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157737666 | CTTCAGTTCTGCTCT[C/G]ATCTTAGTTATTTCT | 51429 |
| rs563764915 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157786348 | GCCACCATGCCTGGC[A/C/T]GATCCTTGCATGTTT | 51429 |
| rs563770228 | in-del | -/A | 0.00676609 | 0.0577691 | intron-variant | SNX9 | GRCh38.p7 | 6:157739251 | AAACAAATTTACAAG[-/A]AAAAAAACAAAAAAC | 51429 |
| rs563785272 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889159 | AGAGACATCAGGCGC[A/C]GTGGCTCACGCCTGT | 51429 |
| rs563830879 | in-del | -/GTAAGTAT | 0.00636936 | 0.0560724 | intron-variant | SNX9 | GRCh38.p7 | 6:157747518 | GCCATAAGTACAGGA[-/GTAAGTAT]GTAAGTATGTTGTGA | 51429 |
| rs563855580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157814623 | CTCAATAATTTTTCA[A/G]TGAGGGGCCCTGCAT | 51429 |
| rs563865265 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157777171 | CCAAGGCGGGTGGAT[A/C]ACGAGGTCAGGAGAT | 51429 |
| rs563875243 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157821077 | AATGAGGTCTCACTA[C/T]GTTGCCCAGGCTGGT | 51429 |
| rs563875980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157908667 | GCTGTTTTAAATAAG[A/G]TGAAAAAACCAGGTT | 51429 |
| rs563903614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157877760 | GGGCACATCCCCTCT[C/T]AGGCATGCATCTCTT | 51429 |
| rs563906061 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157871687 | TATAATAATAATTTT[A/T]AAAAATTTTTAAAAA | 51429 |
| rs563909663 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157863552 | CTAGGTGGAAATTTA[A/G]CTCTTAGAAATAGTT | 51429 |
| rs563910219 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157901465 | TTCTAGGAGTTGTGT[A/G]GTTTCAGGTCTTCCA | 51429 |
| rs563945123 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157828235 | ATTTGTATAGTCAAA[A/G]ATAAGTTCTGTGACA | 51429 |
| rs563947812 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157914615 | CTGAGTAGCTGGGAC[A/T]ACAGGCTCTCATCAA | 51429 |
| rs563950152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157830655 | ATGGTAACTGCCTGC[C/T]TCTTGTGGCTAACAA | 51429 |
| rs563951303 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157771914 | ACGTTGGCCAGGCTG[C/G]TCTCGAACTCCTGAC | 51429 |
| rs563965731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157866478 | ACTGGGGAGGCTGAG[A/G]TGGGAGGATTGCTTG | 51429 |
| rs564009067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157908099 | TTCCTCTTAAAAAAA[A/G]AAATTAGGACTGGGT | 51429 |
| rs564017842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157931015 | TGTCTAATGTCTGAT[C/T]AACTCCATGTCCTGT | 51429 |
| rs564025286 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157924316 | AGATTGGCACCTCCC[A/G]GGGAGCAGTGGTGCC | 51429 |
| rs564027041 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157789546 | AAACTCTACTGTAGA[A/T]GAGAAGACTGTACAA | 51429 |
| rs564060349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157795137 | AACACATCTTGAGGC[A/G]GGGCACGGTGGCTCA | 51429 |
| rs564064500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157837586 | TTTTCCTGTTTGCCC[A/G]CTTAGAAGCTTTAAG | 51429 |
| rs564067476 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157931879 | ATCATGATGATCAAG[C/T]GCGGTGTCGCTAGAA | 51429 |
| rs564086573 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157920077 | AACCACCTCAGGCCA[A/G]TAAGTTGGGGCTCCT | 51429 |
| rs564113011 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157762811 | AAACAACTGGCAGAG[A/G]AAGGCTGCTCGGTGA | 51429 |
| rs564126552 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840949 | TAAGCAAAGTACTTG[C/T]AGACTGCTGGATTTC | 51429 |
| rs564130228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157924963 | CTTACAGAAGATAAC[A/G]TGGAACATCCTCCTA | 51429 |
| rs564150786 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157878418 | TTATGATCTTGGAAT[A/T]TGGAAGCCCACCATT | 51429 |
| rs564151345 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157858768 | AAGGAGAAGCAAAGG[C/G]ACATCTTACATGGCA | 51429 |
| rs564160953 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157805632 | ACAGGACACAAATAA[A/C]AAGTTGGAAACTATA | 51429 |
| rs564175120 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157794336 | GTGGAACTGTGAGTC[C/T]ATTAAACCTCTTTTT | 51429 |
| rs564178208 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157836923 | CCAGTTCCCAGGTGA[C/T]GCTGATGCTGCTGGT | 51429 |
| rs564210209 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157857954 | AATGCGTGGTTCTTG[C/T]GGTCTGGAGAGCCCA | 51429 |
| rs564218154 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SNX9 | GRCh38.p7 | 6:157736324 | TTTGTGTCCTCTCTT[A/G]TTTCCTTGAGCAGTG | 51429 |
| rs564227779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157762112 | GTGCCCTGTGGGGCC[A/G]GGAGGGGCAGAGTAC | 51429 |
| rs564227862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157769019 | CACTCCAGCCTGGAC[A/G]ACAGAGCAAGACTCC | 51429 |
| rs564267242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157773269 | TCAAATACTGACTGG[A/G]TCCCTCCTTGACTGC | 51429 |
| rs564271048 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157869577 | CTTCTCTCCACCCTG[C/T]GCTTCCTGCCAGCGC | 51429 |
| rs564271661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157911106 | CGACAGAGCGAGACT[C/T]TGTCTCAAATAAATA | 51429 |
| rs564291249 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157925897 | CTGGAAGTCGAAGAT[C/G]AAGGCACCAGCATTT | 51429 |
| rs564320903 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157899642 | AGCCGGGTGTGGTGG[C/T]AGGCGCCTGTAGTCC | 51429 |
| rs564354502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157919147 | TATAATGCAGGTCTG[C/T]TATCAGTGAATTATC | 51429 |
| rs564357935 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157917552 | TTGATCCATGGGTTA[G/T]TTAGAAATATACCTA | 51429 |
| rs564368789 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157724824 | ATCTTGAAACTTGGA[A/G]CTTGAATAAACTTTC | 51429 |
| rs564377220 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157810177 | ATGAATGAATTTTTT[A/T]AAATATCATGCTAAG | 51429 |
| rs564390398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893545 | ACAACATTAGGGGCT[A/G]TATTAGACAGGGTGG | 51429 |
| rs564395670 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157831131 | CATTAATAGTTTTCC[A/G]TCCTAATCTCAGAAG | 51429 |
| rs564416750 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157799904 | ATATCACTGCTATAA[C/T]GTGGACAGCCCATGA | 51429 |
| rs564420132 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157918200 | TCAATTATTGAGTAT[C/T]GGGTATTGAAATTTA | 51429 |
| rs564428447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157779700 | TACACAGAGACTTCC[C/T]GTGAAGATTAAATTC | 51429 |
| rs564443906 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157796495 | TCCATCTGGTGGCTG[C/T]GCCATCTGGAACTTG | 51429 |
| rs564454284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886619 | ATGTTATTCCTTCCA[C/T]GCTTAGCTGGTTTCA | 51429 |
| rs564458663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157852113 | CTGAGTCCCTGCTTT[C/T]AGTTCTTTTGAGTGG | 51429 |
| rs564486854 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157844946 | AAATTCCCAAAGTTC[A/G]TTCAGCCTGCGTCCA | 51429 |
| rs564505224 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157765449 | CAAGCTCCGCCTCCC[A/G]GGTTCACGCCATTCT | 51429 |
| rs564505284 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157774735 | CTCTCTTCGCTGCTC[A/C]TCTCCCTTGAGACCC | 51429 |
| rs564512607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157757025 | TGAATTCCACTTCAA[C/T]TTCCACCCCCTCCCC | 51429 |
| rs564572782 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157882765 | CTCATGATAAAACTT[G/T]AACAGATGAGGAGTT | 51429 |
| rs564575144 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885912 | ATGTTTTGAGCTTTC[A/G]TAGACCCTTTGTACA | 51429 |
| rs564576120 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157943963 | TACAGAGTCCCCGGC[A/G]CTCTGAGGTTGGAGA | 51429 |
| rs564578843 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157905083 | CCACAAGGAGATTTC[A/C]GCCCCTAAGGCTACC | 51429 |
| rs564593091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157859444 | TCTTGTTGCTGTATA[A/G]TATTCCATTTTGACA | 51429 |
| rs564614206 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157724237 | GGGAGGGGGCGTGGA[A/G]CTTCCATGCCCTCTC | 51429 |
| rs564614704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157771397 | TTCAAACATCAGCTC[C/T]CTCTTCAGCAAGTTG | 51429 |
| rs564616326 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157715700 | AAAGAAAAAAAAATC[A/G]AGATAAAGCCTAAAA | 51429 |
| rs564619523 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157727061 | AAATGGTCTGTGTAA[C/G]AGGTTAGGAGAAATC | 51429 |
| rs564621095 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157757548 | TATGACATGGCCATG[A/G]CAGAGAAGAGTCACC | 51429 |
| rs564640143 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157899157 | CACCTTATCTGACAC[C/G]GGGATTATTGTCAGA | 51429 |
| rs564661459 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157751436 | AAAAAATTAAAACTA[G/T]AACTACTATATAATC | 51429 |
| rs564672311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157901276 | TCAGGGGGTCTCCCT[A/G]CACCAGCCCATAGGC | 51429 |
| rs564689133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157744426 | TCATGGAATGTATAA[C/T]AAAATGTGTAAGATA | 51429 |
| rs564699953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157855550 | CAGAGTTTTGCTTTC[A/G]TTTTTTGGTAGACTG | 51429 |
| rs564716288 | snp | C/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885747 | GGCCCCATCCCAAGA[C/T]AATAACATAGAAAGT | 51429 |
| rs564717610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157770525 | GGGTGCGGTGGCTCA[C/T]GCTTGTAATCCCAGC | 51429 |
| rs564796461 | snp | C/T | 0.000429114 | 0.0146415 | intron-variant | SNX9 | GRCh38.p7 | 6:157896799 | CAAAAGTCACAAAAA[C/T]TCTCCTTCTTTTTAC | 51429 |
| rs564799049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157908000 | GATTTTAGTCTCTTT[C/T]TAAACTACTCTTATC | 51429 |
| rs564803853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157743831 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCGTC | 51429 |
| rs564825970 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157814248 | TTTTAATGGTTTCCC[A/G]TGGCCTCCCAATGTC | 51429 |
| rs564830752 | in-del | -/T | 0.499779 | 0.0105208 | intron-variant | SNX9 | GRCh38.p7 | 6:157738466 | ATTGCAACCCCTGCT[-/T]TTTTTTTTCTTTCCA | 51429 |
| rs564831065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157719248 | CCTCTGCCATGTCAG[A/G]TGGGCACCCCTGGAA | 51429 |
| rs564838097 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157800095 | CAACTACCATGTAAA[G/T]TGAGAGCAGTTTGTA | 51429 |
| rs564839728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157863380 | TCCACTAATGTTTAT[C/T]TTACTGATAAGTAGA | 51429 |
| rs564867651 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157814533 | GGGCCAGTGTCATGG[A/G]CCTATACAGTTCACA | 51429 |
| rs564884960 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157908188 | ACAAATCTCTCTTCC[C/T]TCAGCGCAATCTGTG | 51429 |
| rs564929764 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157821007 | TGTACTTTTTCATTT[A/G]TTTTTCACAGTCTTG | 51429 |
| rs564949407 | snp | C/T | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157813823 | CTTTCCTTGTAAAGA[C/T]TCAAGCAGAAGGAAC | 51429 |
| rs564968194 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157785578 | ATTCAACAAAAATCA[A/G]CACTCATTCATGAAA | 51429 |
| rs564977281 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157733846 | TTAAGGACAACCCTC[C/T]GGTTATCATCCTGAG | 51429 |
| rs564994377 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157749249 | ACAGGGAGAGAGTTC[A/G]GGGAGATGGGTGATG | 51429 |
| rs565020852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157727595 | TCAGTTACCTTGACT[C/T]ATCTCAGACTTCATT | 51429 |
| rs565024400 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157915757 | TTGAATCCAGGAGGC[A/G]GAGGTTGCCGTGAGC | 51429 |
| rs565037004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157842146 | ATCTTCAAATATCCA[A/G]TCTGTTGGTAGGCAG | 51429 |
| rs565049655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889989 | GGACTAAGAGAGCTA[A/G]GTAAATTACCCAAGG | 51429 |
| rs565065279 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822046 | CCGTCAATGAATGTT[A/G]GCCTCCCAATATTTT | 51429 |
| rs565094729 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157721825 | CTGTTGTTGTTCTTT[G/T]TGGTGCTAGCACCTT | 51429 |
| rs565094735 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | SNX9, LOC107986663 | GRCh38.p7 | 6:157714048 | GGAGGGGCAGGGAAT[C/T]AGCTGTGTCCTGGCC | 51429 |
| rs565102763 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157728375 | TAGTGACACCAACAA[C/T]GGGTGGTAAGCATTC | 51429 |
| rs565117601 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157843419 | ATACGGTATTCTTAC[A/G]GTAAATTAAGCTAAA | 51429 |
| rs565119420 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157876091 | TTTTTTAACTACATA[A/G]AAGGTTTTAAATTCT | 51429 |
| rs565127803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157883354 | ACCAAACCCTCAGCA[C/T]TGCTGACGTATGCTT | 51429 |
| rs565141705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889380 | AGGTTGCAGTGAGCC[A/G]AGATCACACCACTGT | 51429 |
| rs565147623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157909494 | GTTCTTTAAACATAA[C/T]ATCTAACAGGAACAG | 51429 |
| rs565150781 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157850517 | GAGTAACCAACAGTC[A/C]CAGTGCAACTGGGTG | 51429 |
| rs565151930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157807095 | ATGTAAGTAATTTCC[C/T]TCCATCCTTCAAAGA | 51429 |
| rs565156552 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | SNX9, LOC107986663 | GRCh38.p7 | 6:157714692 | CACAGATGCCACACA[C/G]TGGATATCCCAAGGC | 51429 |
| rs565163172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157864581 | GATTCTTGAGGACCA[A/G]TAACACAACAGCAGG | 51429 |
| rs565177150 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157848712 | CTGTGCTGAGCAGGA[A/C]TGACAGGGAGCTTAC | 51429 |
| rs565207931 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157746603 | AGACACCCTCCCATC[C/T]TTATCCTGGGGCAAG | 51429 |
| rs565241282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157734730 | GCGTTATGGGTACAG[C/T]GCATGTCAGTAGACT | 51429 |
| rs565241867 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157933756 | TTTGTCCTAGAGATG[C/G]TGGAATTTTGGCCAT | 51429 |
| rs565242021 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157771995 | TGAGGCACTGCACCC[A/G]GCCCGGCAGCCAAAT | 51429 |
| rs565243469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157942425 | ACACAACCTTCAGGG[A/G]ATTCTGGAAGCTCAT | 51429 |
| rs565244830 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157777836 | AGTGGTGCTCCGTAT[G/T]CAGCTGCTCTCAGCA | 51429 |
| rs565246378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157869920 | ACCTCGCACCCTCAT[A/G]CACCTCTCATGCTCT | 51429 |
| rs565276112 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157816775 | CACATCGTTATAATA[A/C]CTATTAAGATCTGTT | 51429 |
| rs565279412 | in-del | -/ATC | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821673 | ACCTCTTAGAATATT[-/ATC]ATTTTCTTACGGGCT | 51429 |
| rs565280562 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157720828 | GGTTGTTTAACAGTA[G/T]ACTGAGGCAGGAGGA | 51429 |
| rs565293667 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157935293 | CATACTAAAATAAAA[G/T]ATCCAGACAATGGTC | 51429 |
| rs565303718 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157911091 | GCACTCCAGCCCAGG[C/T]GACAGAGCGAGACTC | 51429 |
| rs565306657 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157835169 | AGATGTGTGCCACCA[C/T]GCTCAGCTAATTTCT | 51429 |
| rs565306661 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SNX9 | GRCh38.p7 | 6:157760719 | ATTTGAGGCCCAGAA[A/G]AAATCTAGGATCAGG | 51429 |
| rs565309266 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157934409 | TTATTAGAAAACAAA[C/T]TTAAATCAAAATGGA | 51429 |
| rs565314882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157801095 | GGCGTATGACTTCAG[A/G]TGAGGTTATCTTCTC | 51429 |
| rs565332795 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157740820 | TCTGTGGAAGTAACA[G/T]GGGAAGAATGCAGGC | 51429 |
| rs565342215 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SNX9 | GRCh38.p7 | 6:157744154 | GGTAAATGCTTGATA[C/T]TGAAGACAGCAGCTA | 51429 |
| rs565362355 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157851763 | CCCAGCTAATTTTTT[G/T]TATTTTTAGTAGAGA | 51429 |
| rs565368615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157836717 | TGCCTCAGCCTCCCA[A/G]GTAGCTGGGACTACA | 51429 |
| rs565381764 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157876695 | ACTCACTGTGAAACG[G/T]GAATAGTAGTTATAC | 51429 |
| rs565406963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157829813 | AGCTGAATTTTACCT[C/T]TTTATCCAGTCTGAT | 51429 |
| rs565412635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157902910 | TGGTCTCAAGTGATC[C/T]GCCCGCCTCTACCTC | 51429 |
| rs565420379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157741257 | GGAGGCTGAAACACA[A/G]GAATCACTGGAACCC | 51429 |
| rs565429696 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157858027 | GGTCTCACCTTACAC[A/C]GCTAGGATGATGCGG | 51429 |
| rs565439642 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157735910 | GGGAGGTTGCAGTGA[A/G]CTAAGATAACGCCAC | 51429 |
| rs565445168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157730757 | CAATTCTCCTGCCTC[A/G]GCCTCCCAAGTAGCT | 51429 |
| rs565476570 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157898082 | ACATTCAGGAAGTTA[C/T]AAGAGTTTTAGGAGC | 51429 |
| rs565483339 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157808050 | CAAAGATATTTTCTT[A/T]GTTGAAAATACAAGT | 51429 |
| rs565512499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157845299 | GTATTTTAGTAGAGA[C/T]GGCGTTTCACCATGT | 51429 |
| rs565518115 | in-del | -/GTGTGC | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157899904 | TAAGTGTGTGTGTGT[-/GTGTGC]GCGCGTGTATATGTG | 51429 |
| rs565547166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157910205 | TACATCTATCTGGAA[A/G]TTGCCTAAACGTCTC | 51429 |
| rs565557250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157729224 | GCAGATGAAGGCTAT[C/T]GAGGCTATTTCTTCT | 51429 |
| rs565558771 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157818464 | ACCCAGAATCAATAC[G/T]TTGCATCTTTCGATC | 51429 |
| rs565606668 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157903400 | ACTGCACACTTTTGC[C/T]GCCTCTTACCCAGTT | 51429 |
| rs565613959 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157897614 | CCAGGTTCAAGTGAT[A/G/T]CTCTCACCTCAGCCT | 51429 |
| rs565640584 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157768582 | TGCAATTCAAATGAA[A/C]CCTAACAGCAAATTG | 51429 |
| rs565686696 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157913765 | AGTGTATAGTCTTTC[A/G]AGTCTGACTGCTTTC | 51429 |
| rs565687403 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157810503 | TTGATGATACTGTTG[A/C]GCTGTGGAATCAATT | 51429 |
| rs565687575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157905201 | TCTAGAGAAAGGAGA[C/T]TCAAGGGAAGTCAGC | 51429 |
| rs565689673 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157898822 | AGCCCAAAGCAGGGT[A/G]CAGGTCCCGGCTGAA | 51429 |
| rs565701381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157776891 | ATCCTTCACTTCTCC[A/G]AGGAATCCACTCTTT | 51429 |
| rs565702740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157757170 | CTAGGAAGCACAACA[C/T]AGAAGCAGCTTCAGC | 51429 |
| rs565708546 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157755192 | TGTGCTGACCTCTTA[A/T]CTCATCTTGTGACTT | 51429 |
| rs565715989 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157762384 | TCATTGCTGTAGGGG[A/C]GGAAAGATAATTTTT | 51429 |
| rs565718487 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157769310 | GCCTGGCATCGATCC[A/C/G]ACCAACAATCAACAA | 51429 |
| rs565728445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893868 | AAAAATAAACAGCTA[A/G]GAGATGTTATGCTAA | 51429 |
| rs565759638 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SNX9 | GRCh38.p7 | 6:157776686 | ATGGTTCCTGGTGGC[A/G]TGGGGTGGCCCCAGG | 51429 |
| rs565769697 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157933488 | CAAAATGTAAGATTT[A/C]GGGCTCCCACATGGC | 51429 |
| rs565770589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157774627 | GGCATACTTGGGGGA[A/G]AGCTGGGAGGAGCGC | 51429 |
| rs565787632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157811302 | TCAGTTTGCATTTGT[A/G]TCACCTCCAGAGATG | 51429 |
| rs565791067 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157879186 | ATCTGCTCGCAGAAC[A/G]CAGGTTTCTGGGCAA | 51429 |
| rs565792590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157817829 | GCAGTGAGTCAAGAT[C/T]GTGCCACTGCACTCC | 51429 |
| rs565803842 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157773383 | GTCACATGTCCAGAG[G/T]CACGTGGAAGAAGTC | 51429 |
| rs565806197 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157778485 | CATGTCAAATCCAGG[C/G]AAGAGAGAATTACCT | 51429 |
| rs565814400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157762951 | TTGTCTTTGTGCCCC[A/G]CTTTAGGCAAATAGA | 51429 |
| rs565827900 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157744119 | TGTATATAAAACAAC[G/T]AATCTAATGCCTATA | 51429 |
| rs565828328 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157904728 | AAATAAATAAAATAG[A/T]GTAATTAATAAATAA | 51429 |
| rs565839256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157933013 | AAATGTGTATCTTAC[C/T]CAGGGATCCCTTTGT | 51429 |
| rs565855293 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157880072 | TCACATGCTCTCCCT[G/T]GCATCTCTCTGTTTT | 51429 |
| rs565859352 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886014 | AGCCCTCCTTCGAGG[A/C]CTGATGTAGTTACGA | 51429 |
| rs565867088 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157744655 | GCGACAGCCCCCCCA[G/T]CACTTCAGCCCTCAC | 51429 |
| rs565875919 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157732541 | TCCCTCGCTTCCTAC[C/T]GTTTCCATTTTGTGT | 51429 |
| rs565904024 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157839572 | TTCCATTGCACAGTC[A/C]AAGTGGGGGAAAAAT | 51429 |
| rs565916650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157926044 | TAATCTCATTCACAA[A/G]GGGAGAAGCTCTCAT | 51429 |
| rs565947100 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157715902 | ACCCTCATGACGAAA[C/T]TGGTCAGCCCTGGAA | 51429 |
| rs565949140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157756737 | GCAAAGAAAACCAGG[C/T]CCCCGAGACGCAGGC | 51429 |
| rs565971912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157939142 | CAATTTTTTTGTGTC[A/G]AGAAAAAAAAAAGAT | 51429 |
| rs565986157 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157757907 | TCCCCACAGCTGGAG[C/T]GTAGGTCTCAGGAGG | 51429 |
| rs565994548 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893196 | AAGTGTGACTGCCAG[A/G]CCCTCAGCATGATTG | 51429 |
| rs566017869 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157803328 | CATATTTTAGAAATA[A/T]CAAACAAAAAAGAGA | 51429 |
| rs566040252 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157919315 | TATTTTTTGTCTCAC[A/T]CTCTCTTCTTCCTCT | 51429 |
| rs566042901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157789995 | CATTTCTGGGTCCAC[A/G]CTGGTGTTCGCGTTC | 51429 |
| rs566061086 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157717114 | TCTTGCTCTGTCACC[C/G]AGGCTGGAGTGCAGT | 51429 |
| rs566076824 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157851129 | GGGGCATGGTGGCAC[A/G]TGCCTGTAATCCCAG | 51429 |
| rs566085399 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157826186 | GAAGAACTTTAGTTT[A/G]ACAGTCCTTCACTGC | 51429 |
| rs566086943 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157912963 | AGCTTAGAGATAAAC[C/G]AGCTATGTCAGAAAA | 51429 |
| rs566105021 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157867184 | TCTCGAACCCCTGGC[C/T]TCAAGCAATCCTCCT | 51429 |
| rs566112430 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157941262 | CCCCCGTCACAGCCT[C/G]TCTGTGCCTCTGTGC | 51429 |
| rs566126701 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157876316 | AATTAGCTAGGTGTG[A/G]TGGCAGGCACCTGTA | 51429 |
| rs566148120 | snp | A/T | | | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157715507 | GTATCACTGCTATAA[A/T]CAAGGCTGTAATGAT | 51429 |
| rs566159921 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157812888 | GATAGGAAATACACC[A/C]ATAGAATGGAATCTG | 51429 |
| rs566160700 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157737893 | ACTTATTTATTTCTG[A/C]CTTAATTTCATTATT | 51429 |
| rs566174681 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157781099 | TGAAGATGAGAAAAT[A/G]TTTGAGAAGGATTGA | 51429 |
| rs566186460 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157784906 | GAACATATTAAACAT[C/T]TAAGGAAGAAATGAT | 51429 |
| rs566195178 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157738024 | TCTGAGAGACTGTTT[G/T]TTATGGTTTGCTGAG | 51429 |
| rs566218576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157754806 | AAGAGAGGGTTCTTG[A/G]ATCTTGTGCAAGAAA | 51429 |
| rs566225797 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157763807 | AGTGCCCCCAGTTGA[C/T]GACTGGCAAATCTAG | 51429 |
| rs566229359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157913649 | TCCCCAGGTTCCCTC[A/G]TGCTGCCCATCCCCC | 51429 |
| rs566248300 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157725877 | ACTACCCTTCAATCC[A/G]TTTGAGTTACCTGAT | 51429 |
| rs566337536 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157834926 | AGGAAATCAATACCC[A/G]TTAGGTTACTGAGAT | 51429 |
| rs566337832 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157808582 | TTGCCAGCTCTGTGA[A/G]AATGGATCTGAGCCC | 51429 |
| rs566366561 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157819329 | TTTTGTCTCCCTCAC[C/G]TGTAACAGCATCCAG | 51429 |
| rs566370180 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157878838 | ATACAGGCTAATTCC[A/G]TTCATATACATACAC | 51429 |
| rs566383095 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157725306 | TGAGGTTTCCTTGTG[C/T]GGAGCTACTTAGATC | 51429 |
| rs566388382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157876846 | GCTTCTACCTACCAG[A/G]TGCCAGTCACATGCA | 51429 |
| rs566391949 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157812339 | AAAGTCTAGTGGGCT[C/G]TCCACAAATACATGT | 51429 |
| rs566401685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157820052 | GGTTCTGGGTTCTAA[A/G]GGCAGGCCTGCGTAG | 51429 |
| rs566407364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157792328 | GTATTTCTAGTAGAG[A/G]TGGCGTTTCACCATG | 51429 |
| rs566435884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157746854 | TTCTCTAAGACAGTG[A/G]TCCCCAGCCTTTTTG | 51429 |
| rs566436467 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157900149 | TCTATAAGTTTTTTA[A/G]ATTTTTTTAAAGACC | 51429 |
| rs566438253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157922857 | TATATAGTAGTGAAA[C/T]TAAGTTCTTTGAATT | 51429 |
| rs566443230 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157777935 | CCGTCCTCACCATTG[C/T]CAATGAGCCTATTAC | 51429 |
| rs566451079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157785875 | CAGGACTCTGGCTTA[A/G]TGATATTCCTTGCAA | 51429 |
| rs566456396 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157785112 | TAGCCGGGTGTGGTG[C/G]CGGGTGCCTGTAATC | 51429 |
| rs566479209 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157935781 | GACGAACACAGGCTG[A/G]CGAGAGCTGCCAGTG | 51429 |
| rs566480577 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157829280 | CCTACAAGTTGTCAG[A/C]ATTGTCTTTAATTTC | 51429 |
| rs566498047 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157923579 | AATTTTCTAATACTG[C/T]GTCTCATGGACTGGA | 51429 |
| rs566503343 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157719473 | ATCTTGGAATTAAGC[C/T]AAGGACTTAAAGACA | 51429 |
| rs566530878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890181 | GTCTTGCCCCTTTTT[A/G]TCCCATATTGTATAT | 51429 |
| rs566539771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157842342 | AACAGTTAAAAAATA[C/T]ATGCATGTCTTGCTT | 51429 |
| rs566546658 | snp | A/G | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157800443 | AGGAGTTTGAGACCA[A/G]TCTGGGCAACACGGC | 51429 |
| rs566568350 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157765424 | GCAGTGGCGCGATCT[C/T]GGCTCACTGCAAGCT | 51429 |
| rs566570875 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157929491 | TCTCTCCTTTATATC[G/T]GGTCTGCCCTTATTG | 51429 |
| rs566596824 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157775358 | GAGACTCTGTCTCTC[-/A]AAAAAAAAAAAAAAA | 51429 |
| rs566597957 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157810758 | GATGCAATCTCTCTC[C/T]GGCAAAGCTCATTTA | 51429 |
| rs566638253 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157730891 | TGATCTGCTGGCCTC[A/G]GCCTCCCAAAGTGCT | 51429 |
| rs566645599 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157864678 | GCCCGTCCCCTGCCC[A/G]CATTTCTGTCCTGTC | 51429 |
| rs566654122 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157858342 | GCCTCCACCACCCGG[A/G]TTCAAGTGATTCTCC | 51429 |
| rs566657062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157898266 | TCATTAACTCTAACT[C/T]TAGTTCAGTCTTACT | 51429 |
| rs566665105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157801309 | GTGAGCATTTATATG[C/T]TACATATTTTTTCAT | 51429 |
| rs566675502 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157864304 | CCTCCGTGACCTAAA[C/T]GCCCCCCATTTGCCG | 51429 |
| rs566679342 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157815742 | TGTCCTTTGCAGGGA[C/G]ATGGATGAAGCTGGA | 51429 |
| rs566698370 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157767367 | CCACTTCACTGCTCC[A/G]AGTTTTCTCATCTGT | 51429 |
| rs566719978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157857542 | TTTTTTCCTTCAGAT[A/G]GTTACTTATTTGTTC | 51429 |
| rs566720476 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157761557 | TTGTACCCTGCACAG[C/G]AAAAAGGGGTTGTAA | 51429 |
| rs566741606 | snp | A/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885894 | GCTGCGACCACTCAC[A/G]GTATGTTTTGAGCTT | 51429 |
| rs566764670 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157830058 | TAACTCCAGTCATCT[A/C]CCCCAATATGATCAA | 51429 |
| rs566766735 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822220 | CAGGTCAAATAGAAT[C/G]TATTTAAGAAGACAC | 51429 |
| rs566769149 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157734906 | TCCCAACTGGATTCA[A/G]GCTAAGATGCTACCA | 51429 |
| rs566782171 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157769308 | GAGCCTGGCATCGAT[A/C]CGACCAACAATCAAC | 51429 |
| rs566786786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157794542 | CTTGAACTACTACAT[C/T]GTTTTGTCCATAGAG | 51429 |
| rs566803701 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157823071 | CGGCGGTGACTGCCC[A/G]GGGCGGCGGCGCGGC | 51429 |
| rs566806153 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157908165 | GCCTCTCTGAGGTCT[C/T]AGCCGAAACAAATCT | 51429 |
| rs566819361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157932048 | AATCAATTGAAAAAA[C/T]AATCACTTTTGCAAC | 51429 |
| rs566828931 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157937648 | TAATTCCCATTAGAA[A/G]GGTTTTGTAACTGAA | 51429 |
| rs566844584 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157850698 | TTCATTGTCAAGCTC[A/C]ATACATCTGATAATG | 51429 |
| rs566851280 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157891486 | AGGCAAATCTGATTT[C/G]CTCCTTTTGGTGATC | 51429 |
| rs566857517 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157937137 | TGTTTGTGTGTAAAC[A/C]TACAGCATTAGCTGA | 51429 |
| rs566859425 | snp | G/T | | | downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157945250 | AGATGACTCACAGAG[G/T]CACTGGGTGGAACAA | 51429 |
| rs566886564 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157796208 | CAATGCTGTTTCTTG[G/T]ATAAATCTCACACAT | 51429 |
| rs566896267 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157933651 | ATGGAAGAGCTGAGA[G/T]CAAGCCACGCCCATT | 51429 |
| rs566902941 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157792636 | ATTAACTAAAGGCAC[A/C]ATTTTCTACAATAGA | 51429 |
| rs566907124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157804861 | GGGAGGGAGGAGCCC[A/G]CCTTTACTGCGGTAG | 51429 |
| rs566917534 | snp | C/T | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157838346 | TATTCAACAGTCTCT[C/T]TCTAGAATTTATACT | 51429 |
| rs566936935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157760937 | GTCTGGCAACACAGC[C/T]GGGGGAAAAGAGATT | 51429 |
| rs566967761 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157742606 | CCCAGGCACCACTCT[C/G]ACACTCTTCCCAGCA | 51429 |
| rs566967953 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157853603 | GTTTCATAGGTGACT[A/G]ACTGGGTAGGGGAAT | 51429 |
| rs566975749 | in-del | -/AGTC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157861926 | ACTGCCATACCTGAT[-/AGTC]AGTCTACTAAATGGG | 51429 |
| rs566983049 | snp | C/G/T | 0.0146672 | 0.084371 | intron-variant | SNX9 | GRCh38.p7 | 6:157858249 | TTTCTTTTTCTTTTT[C/G/T]CTTTTTTTTTTTTTG | 51429 |
| rs566984773 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157883473 | AGGAGAAGGTCTTTG[G/T]GTATCAGAGTTAGGC | 51429 |
| rs567003047 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | SNX9, LOC107986663 | GRCh38.p7 | 6:157714265 | CTGCTTCCTGCCTGA[C/G]TGAATTTTCCTTTCT | 51429 |
| rs567050481 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157878590 | GGTGCCCGCCACTAC[G/T]CCCAGGTAATTTTTG | 51429 |
| rs567069504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885132 | TTAGTGTTTTAATTA[C/T]CTTTATTTAAAAAAT | 51429 |
| rs567070167 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157804289 | CAGCTTGTTTATGGT[A/T]TTTATGTCCTGGTTT | 51429 |
| rs567082341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157928219 | CAGGTTATTGTCTCC[A/G]TTTCATGGAGTACTT | 51429 |
| rs567089378 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157834454 | TGGGCTTAAGTGATT[C/G]TCCCACCTCAGCCTC | 51429 |
| rs567111222 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157728722 | AGGGACCTCTGTTAT[C/T]TCCCCCAGTGCCCAC | 51429 |
| rs567123913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157940216 | ACCCCAGCTGCCTGC[C/T]AGGTCCAGTGCAGAC | 51429 |
| rs567125996 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157728119 | AGCGAGGTGCAAGCT[A/G]GGATGAAGAGATGTT | 51429 |
| rs567128939 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SNX9 | GRCh38.p7 | 6:157827856 | AGATTCTAGGAGTTC[C/T]TGATGCTTTTTTTTT | 51429 |
| rs567130516 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | SNX9 | GRCh38.p7 | 6:157835017 | ATAGACATTTTAAAT[A/T]TAATTTTATTTTTGA | 51429 |
| rs567135897 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157745904 | TCTCTTCTCCAGTTA[C/T]GTATGTGAAAGCATG | 51429 |
| rs567182544 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157741962 | CTGGCCCAAGGAAAG[A/T]GCCCAGAAAAGCAAA | 51429 |
| rs567183050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157846767 | AAAGGTTCTTCTTGG[C/T]GGAGTGTGGTGGCTC | 51429 |
| rs567219164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157717690 | TAGGTCACGTGCAAG[A/G]AACTGAGGCTGAGCC | 51429 |
| rs567225197 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157846095 | CTGATGAGATTGTCT[G/T]CGGCTTCTCTGCCTT | 51429 |
| rs567234887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157758047 | ATGGTGGTGCATGCC[C/T]GTAGTCCCACTTACT | 51429 |
| rs567242949 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157853845 | TACTGGGCCATATGT[G/T]CCGGTCCCTATTCTA | 51429 |
| rs567278005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887112 | CTATATGCTGGATAT[C/T]TTTGCATTCCCATAA | 51429 |
| rs567297703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157727196 | TCGTGGCCCAATAAC[A/G]AGAAGCAGACAAACT | 51429 |
| rs567339592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157772491 | AGAGAGTGGGGTGAT[A/G]CATCCGCAGGCTAAG | 51429 |
| rs567348971 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157730634 | ATTTGACTTATGTCC[C/T]TTAGTTCTTTTTTTT | 51429 |
| rs567365757 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157734566 | ATAAATTTATCCTCC[C/T]GCATTTTCCTGCTTT | 51429 |
| rs567369889 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157854933 | TTTTTAATTTTTTTG[A/G]CGGGATAATAGGTTC | 51429 |
| rs567391470 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157864859 | GTGGTGAAACCTCGT[C/T]TCTACCAAAAATACA | 51429 |
| rs567399315 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894043 | GGTATTAGGGTGACC[A/G]ACTGAGGACAAGATG | 51429 |
| rs567411887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157920371 | TTGTCACTGCCACTG[A/G]CACCACCATTGAACA | 51429 |
| rs567427651 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157840438 | TCTTTCTTTTCTTTC[C/T]TTTCTTTCCTTTCCT | 51429 |
| rs567451388 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157796496 | CCATCTGGTGGCTGC[A/G]CCATCTGGAACTTGC | 51429 |
| rs567452721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157791640 | CAAACTGCAGGTGTT[A/G]CAACAAAAATGTGGC | 51429 |
| rs567487605 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157760062 | TTTTTCAGTAGAGAT[A/G]GGGTTTCACCATGTT | 51429 |
| rs567491641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157848373 | TTAGGGGAAAATTCT[C/T]CCCCCAAACCGTGGT | 51429 |
| rs567494627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157775313 | CAGTGAGCCGAGATC[A/G]CACCACCACACTCCA | 51429 |
| rs567496419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157783919 | GAGTGCTGGGATTAC[A/G]GGCGTGAGCCACCGT | 51429 |
| rs567513245 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157867119 | ATGCCCAGCTAATTT[G/T]TCTTTAATTTTTTGG | 51429 |
| rs567520548 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157820145 | TTGATCAAGTGGGAG[C/T]AGAAGACAAACGCCA | 51429 |
| rs567539470 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157795175 | AATCCCAGCACTTTG[A/G]GAGGCCAAGGCGGGC | 51429 |
| rs567555756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157752607 | CCTCCAGCCCTAAGA[C/T]GTTTTTCTCCTATCT | 51429 |
| rs567584997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888675 | GGTAAATTTCAAACT[C/T]GAACACAAGAGGAAA | 51429 |
| rs567600625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157759524 | ATATGGTGAAACCCT[A/G]TCTCTAGTAAAAATA | 51429 |
| rs567605175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157727715 | GTGTTTCATTTCTGG[C/T]TTTGATGTCTGGGCA | 51429 |
| rs567638068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157914242 | GCATTTCCTGATGGC[A/G]AGTGGGGTTGAGCAT | 51429 |
| rs567638522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157868970 | TCCCTCGTGACCGTC[A/G]CTCATACTTAATGTG | 51429 |
| rs567658451 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157755540 | AAAGATTAAAGAAAG[A/C]AAAGGCCACTTTCCC | 51429 |
| rs567672016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157908177 | TCTCAGCCGAAACAA[A/G]TCTCTCTTCCTTCAG | 51429 |
| rs567677557 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157767489 | CATGGCGACCCTCTA[A/G]CAGCCATGAAGTCTG | 51429 |
| rs567678823 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157868355 | CATATGTACACATAG[A/C]TACACTCATCTTCAG | 51429 |
| rs567698267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157941123 | CAGGATTTTTTTAAT[C/T]TCCTAATTCCATCTG | 51429 |
| rs567700578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157863457 | TTCATGTCATCTGTA[A/G]TACTTTTTGAAAGGA | 51429 |
| rs567702017 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157771516 | TAACTTGTATTTTTA[A/C]AAATAGTATAGCTGC | 51429 |
| rs567702801 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157739713 | CAAATGCCCATCAAT[A/G]ATAGACTGCATAAAG | 51429 |
| rs567703017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157803814 | ATGAACATGTATTAC[C/T]GTACAGGGCTCATTA | 51429 |
| rs567752901 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889712 | CAATTAAAAGTCTCT[A/C]TTAATATGACCTGGC | 51429 |
| rs567757473 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157847258 | CAGGTGTGCACCACA[C/T]TGCTTGGCTAATTTT | 51429 |
| rs567763144 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157866085 | TATGTATTATATATT[A/T]TAAAGGTATATATAA | 51429 |
| rs567766516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157735843 | TGGTGGCACACACCT[A/G]TAATTCCAGCTATTT | 51429 |
| rs567776137 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157776064 | AACAGAAGGAAAATG[G/T]AAACTGGAATTCAAG | 51429 |
| rs567788382 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157938820 | TTTCCCTTGATAGAG[A/C]GAAATCCAGATGTGA | 51429 |
| rs567789008 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157802273 | TCCAATCTGGACCCA[A/T]CTGTGTATGGAACAG | 51429 |
| rs567793753 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157914780 | ACCACACTAGCCTTG[G/T]TACTTTCTTAACAGT | 51429 |
| rs567804024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157841882 | TTTTATTTATAAAAA[C/T]TTTAAACATGGACAA | 51429 |
| rs567806773 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157911385 | GTCAGGGAAGACAAG[-/A]GGCGGTGGAATTCTC | 51429 |
| rs567806810 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157907658 | GGTTCCAGCCTTTCA[C/T]TGACCGGCAAGTTTT | 51429 |
| rs567806874 | snp | C/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889379 | GAGGTTGCAGTGAGC[C/T]GAGATCACACCACTG | 51429 |
| rs567809506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157830745 | CACATGTGGCTAATG[A/G]CTACTTTATAGGTGA | 51429 |
| rs567820131 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157941934 | GTCAGTTGGTGCCAT[C/T]GTGGATTTGCCTTTC | 51429 |
| rs567835634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157799757 | ATGAGACTTATTCAC[C/T]ATCACAAGAATAGCA | 51429 |
| rs567849106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157718717 | CTGATTCCATCTCTT[A/G]GATGACACAGGGTTT | 51429 |
| rs567853361 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157763940 | ATTTCTACGGCAGTG[A/G]AAGAGAGCAAAGCAG | 51429 |
| rs567865594 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157907087 | AGCTGAAGAGCTGTA[A/T]CCAAGAGCCCTTTTT | 51429 |
| rs567866472 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157796959 | TTATAAATACTTAAA[A/C]AAATTTTAATTACTA | 51429 |
| rs567872338 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157898189 | AAATAGATTTTATTC[A/G]AAAGAACTGCTTGCA | 51429 |
| rs567872870 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157941550 | CTATAGAAAACAAAA[A/G]TCTAGTAGCATGTCT | 51429 |
| rs567883695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157936161 | CTTTTCTGTTTCTGT[A/G]TATCTTTTTTAATTG | 51429 |
| rs567891897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157929142 | CAGCAGAAGCACTGC[C/T]GAGGGGAGAGTGTCG | 51429 |
| rs567895462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157896470 | TGTACATGTGCAGCT[A/G]AAGTATGAAAACACA | 51429 |
| rs567901198 | in-del | -/CA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157870341 | ACCTGCGCTCACACT[-/CA]CACTCATGCTCTCAC | 51429 |
| rs567919472 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157938557 | TCAGTTATAGAATAT[A/T]TTAGCATTGTTATAT | 51429 |
| rs567923843 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157765591 | CGATCTCCTGACCTC[A/G]TGATCCGCCCGCCTC | 51429 |
| rs567930382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157901578 | CTGGTTTTCCCAGCA[C/T]GACTTACTAAAGAGA | 51429 |
| rs567959229 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889090 | ATTATTGCATGACCA[A/C]ATGTCTGCAGTTGAG | 51429 |
| rs567981865 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157916281 | CCTCATGATTCACCC[A/G]CCTCGGCCTCCCAAA | 51429 |
| rs567990617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157761843 | TTCAAGAAGGGGGAA[A/G]GAGAGCCCAGGGCCA | 51429 |
| rs568003341 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157914069 | GAAATTGCCCAACTG[G/T]TTTTCAAAGAAGCTA | 51429 |
| rs568012528 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157942873 | AGAATGCCGCGTGCT[G/T]TCTCCTGACTTGGGG | 51429 |
| rs568014080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157910777 | TTGTTTTTAATCTCC[A/G]GCCTAGGGTAGACTC | 51429 |
| rs568023500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157858809 | GAGCTTGTGCAGGGG[A/G]ACTCCCCTTTATAAA | 51429 |
| rs568042820 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157895856 | GATGCTCCATAGTCA[A/C]ACTGAAACTTGAAGG | 51429 |
| rs568081064 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157772542 | AGCGCCTGAAACAGA[C/T]GAGGTGAGGACGAAT | 51429 |
| rs568126152 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157715884 | AAACAGTGAATTAGA[A/G]CAACCCTCATGACGA | 51429 |
| rs568139260 | in-del | -/AATT | 0.00874735 | 0.0655527 | intron-variant | SNX9 | GRCh38.p7 | 6:157868742 | AACAAAAATTGTATC[-/AATT]AATAGTATTTCATTG | 51429 |
| rs568144372 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157780733 | TTTCTTTCTTTCTTT[A/C]TTTCTCTCTCTCTCT | 51429 |
| rs568171691 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157870550 | CACCCCTCAGACACT[C/T]TCACCTGCTCTCACA | 51429 |
| rs568181952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157824025 | TTATTTTTTTCTTTT[A/G]TTTTGCTACCTTTTC | 51429 |
| rs568193724 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157852216 | GTACCATTTTATATT[A/C]CCACCAACCATTGAT | 51429 |
| rs568196420 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157905240 | CAGGAAAAGAAGACA[C/T]GGGCCCCTGAGAGCA | 51429 |
| rs568228555 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157760157 | ATTACAGGCGTGAGC[C/T]ACCACGCCCGGGCCA | 51429 |
| rs568236822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157938501 | TTTAGATGCTTTCCT[C/T]TCTTCTTATTTTGTG | 51429 |
| rs568242889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157768466 | CAGATGAACTGGCAC[C/T]GTTGACACCATACTT | 51429 |
| rs568244824 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157898320 | AAACGCTGGGTTGGT[A/G]AAGTAAAAGCAGAAT | 51429 |
| rs568254314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157892562 | TAAGATCACATACAT[A/G]ACCAACTAGTATGAC | 51429 |
| rs568264987 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157723454 | AATGCCTGAGCCTGC[A/G]AGAGCTAAACTGTCA | 51429 |
| rs568268402 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157912798 | TGAATATAGTTTTAT[A/T]CCTGGTACCAAACTG | 51429 |
| rs568278882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157844543 | TTGTAGCCTCCAGCT[A/G]CATGACTCCTAAATC | 51429 |
| rs568296315 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157932328 | TATGTAGACCTGTCA[A/C]CTGCTTAGGATCCTG | 51429 |
| rs568300258 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157717347 | TGATCCACCCCACCC[A/G]GCCTAGCTAAGTTAC | 51429 |
| rs568334994 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157722555 | CCACAGCCATTTTGC[G/T]CCAGCCTACAGCATT | 51429 |
| rs568353172 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157720192 | TCCTTTAAAGATAAA[C/G]AGCTCTCCCCTTCCA | 51429 |
| rs568355512 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157943553 | TTTCTGATGTGCTGC[C/T]CTTATGTGAGGACCA | 51429 |
| rs568360202 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157789111 | AGGTAGGAGAATGGC[A/G]TGAACCCAGGAGATG | 51429 |
| rs568365150 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157738423 | TTTTATCTTTGTTGG[C/T]TTAAAGTCTGTTTTA | 51429 |
| rs568368085 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157929287 | GAACTGTGCAGCTCT[C/G]TCACCACACATGTGG | 51429 |
| rs568370314 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157817598 | GGCGTGGTGGCTCAC[A/G]CCTGTAATTCCAGCA | 51429 |
| rs568372791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157879914 | GAGGTTTAAAAGCTA[C/T]TTAAAAGTTCTGTAA | 51429 |
| rs568376539 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157743985 | CAGCACCACTGTACT[C/G]CAGCCTGGGTGATAG | 51429 |
| rs568397534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157912253 | ACTTGGTTAGCACAG[C/T]GTGTGCTCCACAGTG | 51429 |
| rs568412984 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157849254 | TCAAGAAAAAAGAGG[A/G]TACAGTTAATTACAC | 51429 |
| rs568430082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157781688 | AGATTTCGGAGTTTA[C/T]AGCTTCTTTTATTTT | 51429 |
| rs568433631 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157831688 | TTTCTGCTTTCACTT[C/T]CTTTGTGGCCTCTCC | 51429 |
| rs568451700 | in-del | -/TCTC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157831175 | TCCGTTTCTGCACAT[-/TCTC]ACTCATGGTGCTTTG | 51429 |
| rs568456681 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157942611 | GGCCCCAGCGCTGCC[A/G]GTGTCATTCGGGGTT | 51429 |
| rs568458974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157905434 | GCCCTTTGGATGGCT[A/G]TGTTCTAGCTGTCCT | 51429 |
| rs568462097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157918706 | TGTTAAATATTTTAC[A/G]GTGTATTGTTTTAAT | 51429 |
| rs568476125 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157806216 | AGAAAAAATAGAAGG[A/C]ATTTCTTTTCCTTGG | 51429 |
| rs568508482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157792273 | CCGCCTCCAAGTAGC[C/T]GGGACTACAGGCGCG | 51429 |
| rs568510285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157882481 | ACATTTCGCAAGGCT[A/G]TGGCTGCCATAAATA | 51429 |
| rs568514133 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157920617 | TCTCAGGTGGCCATT[C/T]GCCTTTTGTTGATTT | 51429 |
| rs568518592 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157873072 | AACTGTAATCTTTTT[-/C]TTTTTTTTTTTTTTT | 51429 |
| rs568524024 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157924307 | TATGAAACAAGATTG[A/G]CACCTCCCGGGGAGC | 51429 |
| rs568542664 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157867145 | TTTGGTAGAGATGGA[A/C]TCTCGCTTTGTTGCT | 51429 |
| rs568543741 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157786584 | TTAAAGATTTTAGCA[A/T]GGTCTCAGGATACAA | 51429 |
| rs568546475 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157838558 | CATTTAGCCATTGGA[A/C]ACTTAAGAGTAAAAA | 51429 |
| rs568548128 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157718384 | GGTTGTACTAACTTC[C/T]ATTCTCACCAACAGT | 51429 |
| rs568551153 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157724521 | CTTCCAACCACTGAC[C/G/T]CTTCTTGTAGATTAA | 51429 |
| rs568551714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157788445 | ATTTCATTATTCTCA[C/T]TCAAAATCTCTTATA | 51429 |
| rs568587016 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157765651 | TAGGCCACCGCGCCC[C/T]GCCTGAAATGTATTT | 51429 |
| rs568590918 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157769485 | TCCTGGAGGACAGGG[G/T]ATGTTGTGCTGAAGT | 51429 |
| rs568604770 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | SNX9 | GRCh38.p7 | 6:157726515 | TTGAATACCTGGTAA[-/T]TTTTTTATTAGATGT | 51429 |
| rs568613655 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157721636 | ACCCTCTTCCCCACC[A/G]CGGCTCTCTCCTCTG | 51429 |
| rs568619647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157791747 | CTCTTGCATTGCACG[A/G]GGGTAATGATTGTTT | 51429 |
| rs568646863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889651 | TGTATCTGAAGGTAA[C/T]AGAACGTTGGCTGGA | 51429 |
| rs568650129 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157919244 | AGAAAGCAAGTCAGC[C/T]GTTAATGCTGTTTAT | 51429 |
| rs568667305 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157908328 | TGAGTGAATCTGCTT[C/G]CTGAATAGTGGTCCT | 51429 |
| rs568667356 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157777357 | TGCACTCTGGCCTGG[G/T]AGACAGAGCGAGACT | 51429 |
| rs568673068 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157748728 | AGTGAGAATCTGTAT[-/C]AAAAAAAAAAAAAAA | 51429 |
| rs568683896 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157944774 | TTTGGATTTGACTGG[C/T]GTGAGGCAAAGTGAA | 51429 |
| rs568684659 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157872970 | TTTAAGATTTTGAAC[A/G]GTGTTCTCTAGGAAT | 51429 |
| rs568695656 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157732243 | GGACATCACAGAGCC[A/G]TTCTCACAGCACTCC | 51429 |
| rs568715713 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157860752 | AGAGCTGTTCTGCAC[A/G]AGTGAACTACAGAGA | 51429 |
| rs568721814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157737846 | CCAGAGATTCTCATA[C/T]GTTGTGTCTTTGTTC | 51429 |
| rs568728693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157825795 | TTCCCAGAGAGTCAA[A/G]TTGGTGCTTTCCTCC | 51429 |
| rs568733956 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SNX9 | GRCh38.p7 | 6:157746166 | AGTGACTTTTTTGTT[A/G]TTGTTAGGACTAGTC | 51429 |
| rs568744136 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157785001 | TCTGTAATCCCAACA[A/C]TTTGGGAGGCCGAGG | 51429 |
| rs568744166 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157807970 | GCTAAAATTTTAATA[A/T]GAAAATTAGTCTCAC | 51429 |
| rs568760632 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157866815 | AATCTTAGATGTGTG[G/T]GCGTGTGTGTATGTC | 51429 |
| rs568762487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157833225 | GTTTTTTTATGTTTT[A/G]GTTTGTTTTATAGTC | 51429 |
| rs568778163 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157784136 | ATCTTTAAAAAAAAA[-/T]TGAGCAATATAAACC | 51429 |
| rs568782741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157731613 | TTCATCTGACCTCCT[A/G]TAGTTCACCTGGAAT | 51429 |
| rs568786071 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157921968 | ATAGGAGGATAGGCC[C/G]CAAACTCTGAAGGTA | 51429 |
| rs568807437 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157738394 | TTACCTATGTAATGC[C/T]CTTCTTTGTCTTTTT | 51429 |
| rs568807809 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157753950 | AAAGCCAGTAAGCCA[C/G]GAGTACTGGTTGGTC | 51429 |
| rs568830884 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157799044 | TCAGGAAACTTACAG[C/T]CATGGTGGAAGGGGA | 51429 |
| rs568839474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157835161 | GGGATTACAGATGTG[C/T]GCCACCACGCTCAGC | 51429 |
| rs568841385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157841763 | TCCCACTTATCTTCA[A/G]AGTGCATGCTGAGGC | 51429 |
| rs568843924 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SNX9 | GRCh38.p7 | 6:157902603 | CCTGTGCCTAAAAAC[A/G]TGGTCCGGAGCTTTG | 51429 |
| rs568844924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157753187 | TTTCTCCACACAGGA[C/T]AGATCTTATGTTAAG | 51429 |
| rs568846796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157746652 | CCTGGCCGGAAAGAG[A/G]GGAAGGAGCCTTTGC | 51429 |
| rs568878506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157835591 | AAATCTCATCTTGAA[C/T]TGTAATCGCTGTAAT | 51429 |
| rs568886376 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157936215 | TAAGACAAAGTGGAT[A/G]AATACATTTGTCATC | 51429 |
| rs568898636 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157794367 | CTTTATAAATTACCC[A/T]GTCTCAGGTATGTCT | 51429 |
| rs568899163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157896356 | CAGTTAGAAATAGGT[C/T]CTCATGTTGAGTGGG | 51429 |
| rs568899245 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157768135 | GTTCCTCTGACCCTT[C/T]GGTCTCACCATCCAC | 51429 |
| rs568917946 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157831640 | GAGTCTCCCAGCGGG[A/C]AATCCTGCCTCAGCA | 51429 |
| rs568920795 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157875840 | AAAATTGAGAAGACA[A/G]GTATCAAAATATTGT | 51429 |
| rs568935334 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157771978 | TTCTGGGATTACCGG[C/T]GTGAGGCACTGCACC | 51429 |
| rs568943094 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157842470 | GACAGGGGGATTGCA[A/G]TGGAGTAAGAGTAAT | 51429 |
| rs568955204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157841280 | AATTCCACATCTGTG[C/T]GTTTTAATTTAGGGT | 51429 |
| rs568957259 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157797732 | AGGCTCATTGAAGGA[C/T]AGAAACATGTTAAAA | 51429 |
| rs568961440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157793036 | CTGTAAGCTCCACCT[C/T]CCGGGTTCAAGCAAT | 51429 |
| rs568962128 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157902692 | TTTGTTTTGAGACAG[G/T]CGTCTCGCTCTGTCA | 51429 |
| rs568971965 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157815655 | AATAGATAGCTTAGG[C/T]GTGAAATAAGAAGCA | 51429 |
| rs568973473 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157935702 | TCATGTTTTAGAGTC[C/T]TCATCTATTAGGCAA | 51429 |
| rs569008455 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157851910 | TCCTTTTGTGTCTGG[C/T]TTATTTCAATTAGCG | 51429 |
| rs569011039 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157837500 | CCTTTGTGTAAATCC[A/G]GTTTTTAATGTTATT | 51429 |
| rs569019300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157869590 | TGCGCTTCCTGCCAG[C/T]GCCCTGAGCTAAGCT | 51429 |
| rs569054016 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822106 | ATATTATGATGACTA[C/T]AGCTTAACCATGAGC | 51429 |
| rs569057935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157807451 | GCTAATGCAGACCCT[A/G]CTCTCTCTTTATCAC | 51429 |
| rs569073648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157931090 | AGGCCGCTCTTTTGT[A/G]GGGTGGGGAAAGGGA | 51429 |
| rs569074696 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157772033 | ACCAGGATGCTGGCT[C/G]AAGGATGGGTTGGGG | 51429 |
| rs569077898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157837038 | AAGATCTGTGAGGCC[A/G]TAAATTGGGTGGCTG | 51429 |
| rs569100442 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157734819 | GAACCCATGAGGGAA[A/G]GAAAAGAAATTATAT | 51429 |
| rs569102057 | snp | A/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888184 | TCTGGACTCTCTCAC[A/T]TACATGTCTAATGCC | 51429 |
| rs569107956 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157905654 | AAGAAACAAGCACAT[A/G]TGCTGATGAGCAGGA | 51429 |
| rs569114557 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157837779 | GTCAGTAAGAAGTAA[C/T]GGGTGTCTAAATAAG | 51429 |
| rs569128146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157849183 | TAAGTGATAAGGCCA[C/T]GGAGGTGTTCAGGGT | 51429 |
| rs569139246 | snp | C/G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157860751 | CAGAGCTGTTCTGCA[C/G/T]GAGTGAACTACAGAG | 51429 |
| rs569159101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157754941 | GTTGCCCATTTTTAT[A/G]GTTGTTTCTTGATGA | 51429 |
| rs569170909 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157740420 | CTGCTGCCTCATTGG[A/C]AAGCGGACTAGAATC | 51429 |
| rs569188707 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157734456 | TTGTCCTCCTCCCTG[A/C]CTTTTCCACCTAAAG | 51429 |
| rs569194339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157869170 | CTCCCCGGCCTCACT[A/G]GCTGTCCTCTTGTGT | 51429 |
| rs569211418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157930530 | GAAGCTTCATCTCTA[C/T]CTACAGGTGCTCCCC | 51429 |
| rs569237748 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157897659 | ATTACAGGAGCCCAC[C/T]GCCCACCGCCACACC | 51429 |
| rs569241593 | snp | C/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886073 | TGCTCATCTCTGCCA[C/T]GCCACAGTTGCTGTT | 51429 |
| rs569251554 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157907468 | TTTTGTATTTTATAG[C/T]AGAGACGGGGTTTCA | 51429 |
| rs569278845 | snp | A/C/T | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157716521 | TCCTGTGGCACTGGG[A/C/T]GGCGAGCCGTTGTCT | 51429 |
| rs569282797 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890257 | TGGGTGTGCGTGTCC[A/G]TCTCCCCCACCCCTC | 51429 |
| rs569287292 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157939229 | CTGTTGGCGGATGGG[A/T]GGATGGCACTTGGAT | 51429 |
| rs569291865 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157927333 | GACTTTTATGAAATG[A/T]GTGGGATTTGTAGTC | 51429 |
| rs569318229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157923899 | CGCTACCTCACTACA[A/G]TCTGCAGTTGATTTT | 51429 |
| rs569325010 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157728534 | TGTTATCTGTTCTCC[A/G]CAACAAATATGACAT | 51429 |
| rs569340219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157845404 | GTGCGAGCCACCGTG[C/T]CCGGCCCCATTTGTC | 51429 |
| rs569350067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157877111 | CCAGCTATTATCTCA[A/G]GATAGGTGGAGGCAG | 51429 |
| rs569351713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157939567 | CTAAAGATGTGGTAC[C/T]GGGGAGAAGAGAATG | 51429 |
| rs569373799 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157818554 | AACTAGCAAAATGTC[C/G]TATATCCACTGTTAC | 51429 |
| rs569380057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157916324 | CAGGCGTGAGCCACC[A/G]TGCCCGGCCCTCTTT | 51429 |
| rs569381438 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157856829 | CTTTTTTTTTCAAGT[A/T]TATTTCATAAGCAGG | 51429 |
| rs569392265 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157731938 | TGGGACTGCTGGGAA[C/T]GCCAGTCAGGGAAGC | 51429 |
| rs569421688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157793102 | AGGCATGTGCCAGCA[C/T]ACCCAGTCAGCTAAT | 51429 |
| rs569438069 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157747578 | TTGTATTAACTACTC[A/G]TTCGAGGCATATTGC | 51429 |
| rs569475431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157934154 | TATTGTGATTATAGT[A/G]AAAATAACTTCCAGT | 51429 |
| rs569505952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157787399 | ACAAGCCAATTCCTT[A/G]TAATAACTCAATCTC | 51429 |
| rs569524999 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157744700 | ATGATGACAGCATTT[A/T]CCCGGTTCCCTCTGG | 51429 |
| rs569527825 | snp | A/C | 0.00199481 | 0.0315187 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157944728 | GAGTTGCCAAGAAGC[A/C]GACAGTCTCCCAGTG | 51429 |
| rs569541881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157793540 | TTTAAAAAAAGACAA[C/T]ATATATATAAGCTAA | 51429 |
| rs569552220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157899839 | CATGTATATACTGAA[A/G]TCATTACTACAGCCA | 51429 |
| rs569556928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157755280 | GCTCTGTATTCAAGA[C/T]GGAGTTGCTCTGGTT | 51429 |
| rs569578927 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157852985 | TCAGAAAAATTAAAT[C/G]GTGAGTTTTTTTGTT | 51429 |
| rs569592209 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157932435 | TTTGCACCCTCATCC[G/T]AGGACTTTTGAGAAA | 51429 |
| rs569600251 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157852421 | TTTCCATTTTTTCCT[C/G]CCTCCCTCCCTTCCT | 51429 |
| rs569606995 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157846054 | GAGGCGCCCGTCCTG[C/T]TGTGCAGGTGTCTCT | 51429 |
| rs569610803 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157818507 | CACTCAGTTTTAACC[A/G]TCACAGTTTGTAACT | 51429 |
| rs569616985 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157803447 | ATAAACCTAAATGTA[A/T]CCTCACATAGTCTTA | 51429 |
| rs569628540 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157762980 | GAGCGAGGGCAGAGA[C/G]CTCTCCTGCATCTGC | 51429 |
| rs569671586 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157720711 | CAGGGTTGTGAAGAC[A/C]CCTCACAGCCCATTA | 51429 |
| rs569674965 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | SNX9, LOC107986663 | GRCh38.p7 | 6:157715194 | CACGCTCAGGGACAC[A/G]ATCAAGAACATTTTT | 51429 |
| rs569680499 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893245 | ACTGGGGTCATCTGA[C/G]AGTCCATCCCGAAGC | 51429 |
| rs569730062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157917905 | GAACCAACTCTATGT[C/T]TAATTTCCAACTATC | 51429 |
| rs569756801 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157862090 | CTGATAAATTGTTTA[A/T]TTCTGGAATTTTCTA | 51429 |
| rs569812116 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157738567 | CCTGAATACAGCACA[C/G]TGATGCGTCTTGACT | 51429 |
| rs569812221 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157745273 | GCTACGTTATTGTGA[C/G]ATGTAGAAATTCTAC | 51429 |
| rs569830909 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157880137 | GTGTGGTGGGAAGCA[A/T]GTAAGCTTTGCTGTT | 51429 |
| rs569841088 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157833364 | TTATATACCTTCTGT[C/T]AATTTGTTTCAAATT | 51429 |
| rs569850589 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157739142 | CAGCAAAAGAAACTA[A/T]CATCAAAGTGAACAG | 51429 |
| rs569858087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157797413 | ATATGCTTTGACATA[C/T]GGAGATAAAGAAATG | 51429 |
| rs569860630 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157790066 | GGAAGGCAGGGAGGA[C/G]GGGTGCATCCACTCC | 51429 |
| rs569873523 | snp | A/C | 0 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157765170 | ATGGGCGTTACCCTC[A/C]GGGACACCGAGCCCT | 51429 |
| rs569876696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157779316 | TTCCTGAGCCTCCTC[A/G]TGGTATCATTGGGAG | 51429 |
| rs569882046 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157755856 | CAGACTTTGATCTTC[C/T]CAGACATTGCTGGAG | 51429 |
| rs569897082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157919419 | TTCTTCATGTTAGTT[A/G]ACTTCTGTTGATCTA | 51429 |
| rs569897189 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157782171 | CAGAAACTCCTTTTT[C/G]TTGTCTTGTCACTAC | 51429 |
| rs569897322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157790621 | GTAGGAGGTGGACTC[A/G]GTCCTTGGGAGGATT | 51429 |
| rs569902700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157796246 | CCTTAAACTGCCAAC[A/G]GAATGGTGTTTGGAC | 51429 |
| rs569906390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157775203 | ATCTCCACTAAAAAT[A/G]CAAAATTAGCTGGGC | 51429 |
| rs569939781 | in-del | -/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157773935 | TTGGAGAAACTGCGA[-/G]TGAACAATTTGATAT | 51429 |
| rs569962400 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157757080 | ATTTACCAAGATGGT[A/G]CTGCCTCTCTAGTAA | 51429 |
| rs569969753 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157916017 | TGTGGGTATGGATTC[-/T]TTGGTTTTTTTGTCT | 51429 |
| rs569977214 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157776561 | AAAGAGAATGTTGCT[A/G]CTAGAAGCAGGCACC | 51429 |
| rs569987510 | snp | C/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887364 | TCACTCTTGATTCTT[C/T]CGTGTGTGTCTTTCC | 51429 |
| rs570003140 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886970 | CTCTTAAATAGTGCT[A/G]AGTCTTTCATCTCTG | 51429 |
| rs570013917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157880646 | TAACCGAGTGCCATC[A/G]TGAGCCACAGTTATT | 51429 |
| rs570018504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157862744 | TGTGCATTTTAGGAT[C/G]TAGTTTTTTGGTTTT | 51429 |
| rs570020924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157913686 | TAACCATGGCAACAG[C/T]TGATGTGTTCTTTGT | 51429 |
| rs570037462 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157757388 | CGGCACTCTGTTACC[A/G]GGGACACGCTCATTC | 51429 |
| rs570045703 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157906786 | ATTCCACATTTTGAT[G/T]GGTGGTAGATTTTCT | 51429 |
| rs570059649 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157871144 | AGCACTTTTGGAGGC[C/T]GAGGCAGGGGGATCG | 51429 |
| rs570071816 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157847556 | AAATTTCATCCATTT[C/T]GATTGTTGAGTTTTT | 51429 |
| rs570078189 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157914188 | TCATTTTAACCAGTC[C/T]GATAGGTATGCAGTG | 51429 |
| rs570090035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157870139 | CACTCACACATGTGA[A/G]CACACACACCCCTCA | 51429 |
| rs570094847 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157873238 | CATCTTTTTATGAAT[A/T]ATCAACTTACAAGAA | 51429 |
| rs570101893 | in-del | -/G | 0.00636936 | 0.0560724 | intron-variant | SNX9 | GRCh38.p7 | 6:157806643 | ATGTAGTCAGAAGCA[-/G]ATGATTTAAATCACC | 51429 |
| rs570118906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157854774 | TTAATGCAGATTCTG[C/T]TTGCCATCTAATCTG | 51429 |
| rs570150189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157732361 | TGTGGATAAATCCCT[A/G]TTTGAAGAGGTTCTT | 51429 |
| rs570150932 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157870516 | CACACATACATGCAC[G/T]CACCTGTGCAAGCAC | 51429 |
| rs570155201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157864877 | TACCAAAAATACAAA[A/G]ATTAGCTGGGTGTGG | 51429 |
| rs570182265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157782842 | AGTGAGCCAAGATCG[C/T]GGCACTGCAGTCCAG | 51429 |
| rs570185257 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157847623 | TGCTGGGAAGGAGCC[A/G]GGCTATGTATATCTG | 51429 |
| rs570208509 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157741034 | CAATGATTCTTAAAC[C/G]TTGGTGTTCTAAGAA | 51429 |
| rs570244880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157725925 | CAAGAACCTGAGTGC[C/T]GAGAGGACAGGGGTT | 51429 |
| rs570245748 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157741482 | ATCTGCATTTTTAAC[A/T]ATGGCCCCCAGGTGA | 51429 |
| rs570269144 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157746261 | TTCTGCATAATTCTT[C/T]TGTGAAGTCTTGCAA | 51429 |
| rs570269661 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157767833 | GGCTTGGGTTCCCAA[C/T]GTCAGGCCAGAATTG | 51429 |
| rs570293575 | snp | A/G | | | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821856 | CCAGGAGGGCTGCTG[A/G]GTCCAAGGCTACGGT | 51429 |
| rs570300173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157941487 | AAACAATAACGAAAA[C/T]TTAAATTTTTCTTAC | 51429 |
| rs570305684 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157853220 | ATGTTTTTGCTGGGT[A/G]TAGAATTCTAGGTTG | 51429 |
| rs570307069 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157900432 | TCTGGCCAGCAGCCC[A/G/T]CAATGCAACGGGGTT | 51429 |
| rs570310415 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157929091 | AAACCATAGTGTTTA[G/T]AAAAACCAATATAGT | 51429 |
| rs570313706 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157898304 | GTGAAGTCACAGATT[A/C]AAACGCTGGGTTGGT | 51429 |
| rs570326149 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157820674 | GTGAAAGTGCACATG[A/T]TTATCTCTTTTTTTT | 51429 |
| rs570328145 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157850702 | TTGTCAAGCTCCATA[C/T]ATCTGATAATGCTTG | 51429 |
| rs570342204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157907613 | AAAGGGGACTTTGTC[C/T]CAGGTTTGCAGTGGT | 51429 |
| rs570363340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157761659 | GAACCGTGTGACCTC[A/G]GAAGCCGCATCCCAC | 51429 |
| rs570368626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157717928 | GTACAATGAACCCAA[A/G]AGGTGATCCCTCACC | 51429 |
| rs570372840 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157804917 | CAATACCACCCATGA[G/T]GGGGGTGCCCCAGAA | 51429 |
| rs570381033 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157896149 | AAGTAAAGGCCAAGT[C/T]GATCTGTAACTGAAT | 51429 |
| rs570419594 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157865363 | AAAAAAAAAAAACAC[A/C]ACATAACATGACAAG | 51429 |
| rs570422915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157786019 | CTGCATTTTGTATCC[C/T]ACAGGCATTTTCCAC | 51429 |
| rs570424187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157778162 | CCTCATCCCAGCTTC[A/G]GGTGGCTGCCAGCAA | 51429 |
| rs570433428 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157767480 | AATTATTTTCATGGC[A/G]ACCCTCTAGCAGCCA | 51429 |
| rs570458280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157735734 | GCACTTTGGGAGGCC[A/G]AGGAGGGCAGATCAC | 51429 |
| rs570458592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157772520 | AGGACCAGCACAGCC[C/T]GCTGGCAGCGCCTGA | 51429 |
| rs570477319 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157916748 | CTTTCCATTGCTGAA[A/C]CAGCCTTACATGCCT | 51429 |
| rs570480709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157883555 | GAATTTGAGGTTGAA[A/G]TACTTTTCCAAGCTC | 51429 |
| rs570514794 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157760949 | AGCCGGGGGAAAAGA[C/G]ATTTATTTTACAACA | 51429 |
| rs570525445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157836886 | GTGAGCCACCGCGCC[C/T]GGCCGAGAACACACA | 51429 |
| rs570539745 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157876927 | TGCCTAGGAGCAAAG[C/G]CAAGCCAGTTGAGAT | 51429 |
| rs570564148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157830109 | TATATCTTTTTCACC[A/G]CAAATTGAACATTAT | 51429 |
| rs570571098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157786446 | AGTGTAATAAGGCAA[A/G]AAAAGGAAATAAAAG | 51429 |
| rs570593721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157858335 | CACCGCAGCCTCCAC[C/T]ACCCGGGTTCAAGTG | 51429 |
| rs570619347 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157794579 | AAAAACGAACACACA[A/T]CATCTTTATATTTTA | 51429 |
| rs570627996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157722461 | GGCCACAGGATGCTA[C/T]GCCCTCTAGAATTAT | 51429 |
| rs570631918 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157903251 | AATGTTAATCTGTGT[C/T]TGGAAAAATTAAAAA | 51429 |
| rs570637117 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157892501 | ACAAAACCAAAGAGA[C/T]AGAAACAAACATAAC | 51429 |
| rs570655105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157850781 | CACTTTTAAGAGCAT[A/G]TATCTTCTTTGCCTT | 51429 |
| rs570678377 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157719267 | GCACCCCTGGAATGA[C/T]AATAAAATAAGGTTT | 51429 |
| rs570701086 | in-del | -/AAAAAAAA/AAAAAAAAAAAAAAAAAAA | 0.132751 | 0.2208 | intron-variant | SNX9 | GRCh38.p7 | 6:157915822 | GAGTTAGACTCTGTC[-/AAAAAAAA/AAAAAAAAAAAAAAAAAAA]AAAAAAAAAAAAAAG | 51429 |
| rs570701730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157910613 | TCTCCCTTCTCTTGT[C/T]TTTTAAGTGCCACAT | 51429 |
| rs570702859 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157808866 | ACATGTCAACAGTAA[C/T]TGGAATAAAAGAGAG | 51429 |
| rs570713766 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157814383 | TCCTTGTTGTGTCTT[A/G]ATTCATGCCATCCTT | 51429 |
| rs570720328 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157823939 | GGCGCTTCCCGTCCC[C/G]GCCTGCGGGGGCTCG | 51429 |
| rs570725367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157756536 | GGTGTGCCATGTCTG[A/G]GGACAATAACTCCTT | 51429 |
| rs570736145 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157818058 | TCTCTAGAGGGGACA[C/G]AACTAATAGGATATA | 51429 |
| rs570737185 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157808408 | CCAGAGTACAACATA[C/G]AAAGATAAAGAGATG | 51429 |
| rs570762007 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157903687 | AGTGAGGTTCCAGCT[C/G]ATGCCTGGGGGTCTC | 51429 |
| rs570775687 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157754022 | TCAGTTCCTAGGTGG[A/G]AGCCACAAGATCAGG | 51429 |
| rs570790004 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SNX9 | GRCh38.p7 | 6:157786167 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 51429 |
| rs570793449 | snp | C/T | 9.91555e-05 | 0.00704045 | intron-variant | SNX9 | GRCh38.p7 | 6:157932189 | TTATTCCTTTTTGTC[C/T]TTCAGCATTACCCAA | 51429 |
| rs570797046 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157920955 | GGTATTTCAGTTTAA[A/G]TAATTTAAAATACCT | 51429 |
| rs570797146 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157944909 | TTTGATGCCTGGAAG[A/T]TTCTCCTTCAAGTGG | 51429 |
| rs570797897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157749003 | ACCTTCTTACATCCT[A/G]AGGAAGTAGGTAGTG | 51429 |
| rs570806595 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157817177 | AAGCCACCCAGTCTA[C/T]GGTATTCTGTTATAG | 51429 |
| rs570812429 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157844409 | AGTTCCTGGGTGGGG[G/T]CCACAAGATCAGATG | 51429 |
| rs570825337 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157831566 | CAGGACACTTTGTGT[A/G]TTGCCTCCCCTGCCC | 51429 |
| rs570832695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157837968 | TTATTATGCATGAAC[A/G]TCAAGGGATATTGAC | 51429 |
| rs570862016 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157931378 | AACATTAAAAGTTTT[A/C]TTTTTCTCCTTTAAT | 51429 |
| rs570869011 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157838462 | TGTACGGTTGCTGTG[A/C/G]TAAAAGTATGTATAC | 51429 |
| rs570882600 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157884602 | TCTCACTCCCACCCC[C/G]CCGTATGAATTCTTT | 51429 |
| rs570890143 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157790815 | TTCCAGAAGTTGGGT[G/T]TAGGGTTCTGGGAGG | 51429 |
| rs570895209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157801943 | GGAATTGAGGTTGCC[A/G]AGCCCAGAGCATCCA | 51429 |
| rs570898719 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157802615 | AAGAAACTTTCCTGT[A/G]TTATTATAGGATAGT | 51429 |
| rs570912795 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157751274 | TGAGACTTATTCACT[A/G]CCATGAGAACAGTAT | 51429 |
| rs570948890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157843885 | GTCTTTTTTTTTTTT[C/T]TTTTTTTGAGATGGA | 51429 |
| rs570949152 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157781955 | GCAGAAAGAAGCCTC[C/T]TTGGAGCTTCCATTA | 51429 |
| rs570974145 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894491 | AAAAAAAAAAAGCTA[A/T]CAAAAAACTGTATTT | 51429 |
| rs570980853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157825638 | TTCCACATGGTGCTC[A/G]TTTCCATGTTTACAT | 51429 |
| rs570982151 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157900678 | TGAAGTAATTCTTTA[A/T]CATAACATCTGTATG | 51429 |
| rs570988662 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157773969 | TGGACACCCTCTCTG[C/G]AGTTTGGAGAACTGG | 51429 |
| rs570996720 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157730168 | TTTAAATGAGTGAAC[G/T]CTATGCAGCGTGAAT | 51429 |
| rs571005224 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157745573 | GACTTGATCCTTCGT[A/G]GCCCTGTTTGATTTT | 51429 |
| rs571019808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157773442 | TGAGCCAGGCGACCT[C/T]GGCAGGAGCCAGAAC | 51429 |
| rs571034746 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157872259 | TCTGAATAAAAGTTA[A/C]AATTTTTCCTTTGAT | 51429 |
| rs571036823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157866227 | GAGGAAGAGCCTGCA[A/G]GAGCAGTCCCTCCTT | 51429 |
| rs571037362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157895239 | GCTGAAACTGGCTTT[A/G]AGGCCTGCAGTTGCT | 51429 |
| rs571038615 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157905018 | GTTCTTTACATAAAT[C/G/T]TTTAATTCCCTTATC | 51429 |
| rs571068085 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157921846 | GTGTGAAGAACTGCC[G/T]GCCAGAAGGGCTTCC | 51429 |
| rs571073251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157879093 | AGTGATGAAGCTTTT[C/T]GGGGCTGGTTCGGTA | 51429 |
| rs571077637 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157878756 | TAGTGGCCATTAAGG[A/T]TATAATTGATACATT | 51429 |
| rs571093384 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157832435 | GTCTGCAGGGGCACA[C/G]TGCAGGCTCCTGGCA | 51429 |
| rs571120780 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157763396 | GACACAGGTCCCTGC[-/G]GGGGAAGTACCTGCT | 51429 |
| rs571121830 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157831591 | CTGCCCCCACACAGT[C/T]CCCAGAGCACAGAGC | 51429 |
| rs571124117 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157935279 | CCATTTTGCAAACTC[A/G]TACTAAAATAAAAGA | 51429 |
| rs571130879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157914927 | AGGTTTTAGGCTTTT[C/T]GTTTAGATCTTTGAT | 51429 |
| rs571130966 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SNX9 | GRCh38.p7 | 6:157820821 | AGCTGGGACTACAGG[C/T]GCGTGCCACCATGCC | 51429 |
| rs571159002 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157825002 | CCTGTAATTCCAGCA[C/T]TTTGGGAGGCCGCGG | 51429 |
| rs571166865 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157841180 | ATTTGGAGATTCAAT[G/T]AATCTTTATTCTTTC | 51429 |
| rs571176351 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157871325 | GTTCCAGGCTGCAGT[G/T]AGCCAAGATGGTGCC | 51429 |
| rs571178166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157737271 | ATTCGGCTGTGAATC[C/T]GTCTGGTCCTCATTT | 51429 |
| rs571184897 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157928386 | TCACAAAGAATTGTA[A/T]AGGCAGAAAGGAAGC | 51429 |
| rs571198491 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157921098 | CGTTTGTAAGAATGA[C/G]ATTAAATTCCACTCA | 51429 |
| rs571212210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157847533 | CTTTCTGAAAAATAT[A/G]TATTTTTAAATTTCA | 51429 |
| rs571233727 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157752655 | AATCGGGTTTTACAC[C/T]GAGACATTCCATTGC | 51429 |
| rs571241279 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157724881 | TTATTTTAGGTTGAC[A/G]ATATCATTTTATATC | 51429 |
| rs571254250 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157861639 | CAAAAGCTGTGGAAA[C/T]CACTGATATGCAGTA | 51429 |
| rs571266407 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157837877 | AGTTTCTTGTGGGTT[C/T]CGTGAACAGCATATG | 51429 |
| rs571278089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157719626 | AGAGAACTCAGCGAA[A/G]ATAGTGCTGTGACAG | 51429 |
| rs571334292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157793202 | TGATCCACCCGCCTC[A/G]GCCTCCCAAAGCGCT | 51429 |
| rs571335285 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157848525 | TCTTTTAGCTGGGGC[A/C]GTAAACCTAGATGAA | 51429 |
| rs571342961 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157728502 | GGGCTTTTGTACTCC[A/G]GTGTATAAATTTATG | 51429 |
| rs571346091 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157717812 | AGTTTTATTAAATGT[C/T]TTATTTTTATGGATT | 51429 |
| rs571347141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887966 | CAGTTTACCCATCAA[C/T]TGGCTTCTTGGAAGC | 51429 |
| rs571350112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157747762 | TGAAATTACTAATCC[C/T]ATATAAAGTATATTT | 51429 |
| rs571354603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157847003 | AGCCCAGGTAGCACT[A/G]CTACACACCAGCCTG | 51429 |
| rs571361974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157805732 | CAAAATGTTTTTCTG[A/G]ATAATATTTTCACTC | 51429 |
| rs571363523 | in-del | -/AAAT | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157781182 | TCAAGGTCAAAAAAA[-/AAAT]AGTCAACAGCAGCAA | 51429 |
| rs571372748 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157914436 | TTGCAAATAACTTGT[A/C]GCAGCTGTGGCTTGG | 51429 |
| rs571383709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157733310 | CGGTAAAACCCCGTC[C/T]CTACTAAAAATACAA | 51429 |
| rs571394633 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157858640 | ATGTATTAGCATGTT[C/T]TCACACTGCTAGTAA | 51429 |
| rs571399034 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157815869 | CAGGGAGGGGACCAT[C/T]ACACACCAGGGCCTG | 51429 |
| rs571416635 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157751397 | GGGTGGGGACACAGA[A/G]CCAAACCATATCAGG | 51429 |
| rs571421272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157828779 | TACGCCTGGCCACAT[A/G]TTAGGTCTTAATGCG | 51429 |
| rs571437535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157740289 | GAGCTGTGTGATATG[C/T]CAGCCCAGGTCTTGC | 51429 |
| rs571448960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157875264 | TGCATTATAGCTATT[A/G]CCATTCCCCAAAAGC | 51429 |
| rs571450191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157835074 | CTGGAGTGCAGTGGC[A/G]TGATCTCAGCTCACT | 51429 |
| rs571455739 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157776797 | TGGTGGAGTTACTGC[A/G]AAAGCAAAGACATTG | 51429 |
| rs571458655 | in-del | -/TCCTTATTAACCCA | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157896033 | TTCTGTTGTTCTATT[-/TCCTTATTAACCCA]TCCTTAAAAACCAAG | 51429 |
| rs571459456 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157842411 | TGATGCAACTGCCCA[A/G]TGGGTTCACCATCAC | 51429 |
| rs571461869 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157794954 | GGAAAAGATTTGGAA[G/T]AGCAGAATTTAAAAA | 51429 |
| rs571483697 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157914565 | CACTACAACCTTGAC[A/C]TCCCGGGCTCAAGCA | 51429 |
| rs571499688 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157771014 | CACAATAAGCTCATT[A/T]TTCAGGCAACTGTCT | 51429 |
| rs571500869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157805851 | ACATGTATATTCAAC[C/T]ATTCAGCAAAGCTTT | 51429 |
| rs571514207 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157818541 | GCAATGACACATGAA[C/T]TAGCAAAATGTCCTA | 51429 |
| rs571561027 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157746124 | TGGCATCCTGCAGAT[A/G]GAACTCCAGGAATCA | 51429 |
| rs571580249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157864176 | GCGCCTTGAGTGCTC[C/T]CTCCTCCAGGGGTAA | 51429 |
| rs571592829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157720133 | ATGTCTGGTCGCAAG[A/G]TTTGCTATATGAAAT | 51429 |
| rs571652442 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157737770 | TTTTAGATCTTTCCC[A/G]CTTTCTCCTGTGGGC | 51429 |
| rs571665619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157755807 | GTGGAGAACTACCCA[C/T]TGGATGCCTCTCCAG | 51429 |
| rs571677661 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157910132 | TGTAGAGCAGCAGGA[G/T]GCAGGAGTTGGAAAC | 51429 |
| rs571678604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157814929 | TAACTTAGTCTGTAA[C/T]TGCCAAGTTTCAGTG | 51429 |
| rs571680212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157896550 | AAGAAAGAGAGGGCT[A/G]TAGCTGCATCTAATA | 51429 |
| rs571717656 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157766276 | GTGGACCAGGATGGC[C/G]ACCTTACCCAGACTT | 51429 |
| rs571738645 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157869019 | GTACCCTGGAGATAC[A/C]AAGACAGGAAACCTG | 51429 |
| rs571758659 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157836519 | CACAGTCACCAACCC[A/G]GGGAGCTTGTTAAAT | 51429 |
| rs571763814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157942642 | AAGGTCTGTCCAGCA[A/G]CAACGCGGGGCAGGG | 51429 |
| rs571782681 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157754926 | CCCCGAGGGCTGCTG[A/G]TTGCCCATTTTTATG | 51429 |
| rs571793973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157771653 | GTCGCCCAAGATGCA[C/T]GCAGGAGGAGCTGCC | 51429 |
| rs571815082 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157908346 | GAATAGTGGTCCTTT[C/T]ACAGTCCATGTGTTT | 51429 |
| rs571818854 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157931628 | CTCTTCCCTGGTCAT[A/G]CGAAGTCTGACTGTT | 51429 |
| rs571825471 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157942926 | TCCCCTATTATTCAG[A/G]AAAAAAAGGAAACAA | 51429 |
| rs571892639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157760173 | ACCACGCCCGGGCCA[C/T]CAAGGTTATTTACAT | 51429 |
| rs571898360 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157878858 | TATACATACACTCTT[A/G]CTAATCTGTAAGAAA | 51429 |
| rs571899822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157922895 | TATTTGGGTTACTTT[A/G]TAGTTACAGAAACTA | 51429 |
| rs571916782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157743054 | GGAGAGCATCTAGAT[A/G]CTCAGGAATTTTTTC | 51429 |
| rs571917601 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, downstream-variant-500B | SNX9, LOC107986663 | GRCh38.p7 | 6:157715247 | TTGGATACTGATGGC[A/G]TAAAGAATGTCAGTT | 51429 |
| rs571941914 | in-del | -/TGTT | 0.00321672 | 0.0399751 | intron-variant | SNX9 | GRCh38.p7 | 6:157866943 | TGTTAATGAAATAGG[-/TGTT]TGTTTGTTTGTTTTT | 51429 |
| rs571951859 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157800594 | GCCCAGGAGGTCAAG[A/T]CTGCAGGGAGCTGTG | 51429 |
| rs571959307 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157929643 | TTGAATTATGAGTAA[C/T]ATATACCTACTTTTC | 51429 |
| rs571986957 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157937951 | GTACAACTTCAGATA[A/G]CTTAATATAAAACTC | 51429 |
| rs571996029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890206 | GTATATTTGTACCAT[A/G]TGCAGCTTTCCTACA | 51429 |
| rs571997887 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157908952 | GTGGACGTGATACCC[A/G]GGGGTTGGAAGTGAG | 51429 |
| rs572009979 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157891915 | GCAGGTAGGGAGAAT[G/T]GGGAATGCAGCACGA | 51429 |
| rs572015384 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157798107 | TTACCAGAGTCTTAC[C/T]AGCATCAAAAGAAAA | 51429 |
| rs572034418 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157817370 | GCTTTCTGATGAAAG[C/G]CCTGGGGAAGGAGAA | 51429 |
| rs572048798 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157858421 | GAGACGGGGTCTGTC[C/T]ATGTTGGTCAGGCTG | 51429 |
| rs572073024 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157918359 | TCATGAGGTGTCCCC[C/T]ATTGTCTCTAGTAAG | 51429 |
| rs572088664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157802005 | GTTGAGCACACTGAG[A/G]TTTGGATGGGCTCAG | 51429 |
| rs572099837 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157809208 | AGGATAGAGAGCCCT[C/G]AAACAGACCTCATAT | 51429 |
| rs572100950 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157754814 | GTTCTTGGATCTTGT[G/T]CAAGAAAGAATTCAG | 51429 |
| rs572106348 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157774092 | GCCTGCCCAGGGGAC[C/T]GCAAAGGGATAGGGT | 51429 |
| rs572125832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157788501 | TAACTTCTTTTACAA[C/T]TCAGAAAAATCAAAA | 51429 |
| rs572155604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157904097 | GGAACATAAATCTTA[C/T]ACTAGAAAAAGAGAT | 51429 |
| rs572157351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157898050 | TATCAGAACAAAAGA[C/T]ACACCTTGCACACCT | 51429 |
| rs572190446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157779660 | TGAGTTTAATCTTTC[C/T]TACTGGCAAAATGGG | 51429 |
| rs572194034 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157767989 | TCACAGGCCATCAGG[C/G]AGTAGGGGGATCTAC | 51429 |
| rs572202422 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157801751 | TTAAAAAAAAAAAAA[A/C]CCACAAAATATCCAT | 51429 |
| rs572209866 | in-del | -/T | 0.33366 | 0.235586 | intron-variant | SNX9 | GRCh38.p7 | 6:157873073 | ACTGTAATCTTTTTC[-/T]TTTTTTTTTTTTTTT | 51429 |
| rs572211801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157892651 | TTTGCCCTAATTAAA[C/T]GGATTTTAATTTTTT | 51429 |
| rs572218842 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SNX9 | GRCh38.p7 | 6:157898341 | AAAGCAGAATGGGCG[A/G]TGGAGGCTGCAGAAG | 51429 |
| rs572233041 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157843784 | TCTAATTTTTTGTTT[C/G]TTTTAGAAGAGCTTA | 51429 |
| rs572237257 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157925450 | TGAAGTTGAACCCTC[C/T]CATATGACCTGGCAT | 51429 |
| rs572243810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157831044 | TTTGGTTCTATTTCA[A/G]ATCTGCTTATCATTC | 51429 |
| rs572247115 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157736847 | CCTAGTTTATTGAGA[C/G]TTTTTAGCATGAAGG | 51429 |
| rs572271431 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157733199 | AATTTGCCTGGTGGG[A/G]CCGGGCGCTGTGGCT | 51429 |
| rs572309969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157912405 | CACGGTTCTCCTTCC[A/G]TACTAAGATTTGTTT | 51429 |
| rs572324885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157795077 | TATGCAGTATGTGCA[C/T]CTAGTTTAGGTCCCA | 51429 |
| rs572355585 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157868058 | AGATGATGGTGATTT[G/T]CCTAAATGTCTTAAC | 51429 |
| rs572374919 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157924915 | AATTCCATGTGGCTC[C/G]CAGATTTAAATGTGA | 51429 |
| rs572381713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157859419 | CTGAGTATATAGATT[A/G]TTCTCATTCTCTTGT | 51429 |
| rs572386466 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157859950 | AGCAAATTTTGGCCC[A/G]TGAACAAAATCTAGC | 51429 |
| rs572401610 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157801239 | ACTTCTTGTGAAACC[A/T]AACATTATAAGCAGG | 51429 |
| rs572410972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157795662 | GGAACATAGATGAAA[C/T]ATGGTGAAATATTAA | 51429 |
| rs572421279 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157780223 | TTGCAAAATGAGGGT[G/T]GTAAAAACATTTACT | 51429 |
| rs572424259 | snp | A/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157943356 | GAGGGAAGTCGTTAC[A/G/T]CCTTTCACTGCCACA | 51429 |
| rs572434497 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157825963 | TGTTGCTATAAGTAT[G/T]AACTGATGAAAAGTA | 51429 |
| rs572435788 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157731688 | CAGATCCCTTCGACT[A/T]CTAAATATATTTAAT | 51429 |
| rs572442363 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157737545 | GATTCTTCTCTCTTT[G/T]CTTCTTTATTAATCT | 51429 |
| rs572443276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893454 | TTGATGCACCTGGCA[C/T]GTGACAGCCAGCTGT | 51429 |
| rs572454540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157899918 | GTGCGCGTGTATATG[C/T]GCAAGTGCGTGCCTG | 51429 |
| rs572466843 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157907918 | CGAAAGTCATCTCCT[C/T]TGCAGCTTTCAGCTA | 51429 |
| rs572474256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157818897 | GCCTCCCTAGCCTCC[A/G]GTCTCTCTCTGCCCA | 51429 |
| rs572486011 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157876118 | TTCTATCAGGCCTGA[C/T]GATAATCATATCACT | 51429 |
| rs572502842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157771369 | AAGAGCTTTAAAGCC[A/G]TAGAGTTTTAGGTTC | 51429 |
| rs572516045 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157866405 | ATGGTGAAACCTTAT[C/T]TCTACAAAAAATACA | 51429 |
| rs572529419 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157908409 | ATTATTTTTCATTTT[A/C]AAGCCAAGAAGATAG | 51429 |
| rs572536126 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157906687 | GAGCTACCAAATGGA[A/G]GCTGGGAGTTAAAGA | 51429 |
| rs572541651 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157771804 | TCCCAGGCTCAAGCC[A/C]TTCTCCTGCCTCACC | 51429 |
| rs572548908 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157825237 | TGGGCGACAGAGCGA[G/T]ACTCCGTTTGAAAAA | 51429 |
| rs572553202 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157936763 | ACAGGGTAGGTCCTT[A/G]TCATAGCTACATAGC | 51429 |
| rs572558131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157874906 | CAACCCATTAAAATA[C/T]GAGTATGCGGCAAAA | 51429 |
| rs572581458 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157933246 | CTATAGTGTGCCATG[A/G]TCACACCACTGCACT | 51429 |
| rs572600540 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886546 | AAACATACAGATATA[A/T]ATTGTATATAAATGG | 51429 |
| rs572620029 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157875462 | GAAACTGCAAATACC[C/G]TCTTAGATAAAGGCA | 51429 |
| rs572641457 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157811616 | AGATAATGGAGGTCA[A/C]TAGACTACAAACTTT | 51429 |
| rs572647907 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157839767 | CCCCATCTTGCCCTC[C/G]AGTCTCCTCTTTAGG | 51429 |
| rs572648875 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157916576 | TTTTTTGTTAGATGT[A/G]CTTTTATCAAGTTAA | 51429 |
| rs572652865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157866675 | TATGTAAGTCTTGGT[A/G]TGGTGGAAGAGTACC | 51429 |
| rs572694695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157716235 | GCAAGGTAAGAAGAA[A/G]GTGGCTAAGGCTGCC | 51429 |
| rs572699077 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157806526 | TTAAAAAATATAAAG[C/T]AAATCAAACGTCCAT | 51429 |
| rs572706018 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157846112 | GGCTTCTCTGCCTTC[C/G]CATCTGATGCATCCC | 51429 |
| rs572712186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157851591 | TGGAATCATATATTC[A/G]TTGTTTTTTTCTTTT | 51429 |
| rs572714404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157820939 | CGCAGCCTCCCAAAG[C/T]GCTGGGATTACAGGC | 51429 |
| rs572714798 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157939367 | AAATAAATTTTGATT[G/T]TGAAGGAACTTGAAA | 51429 |
| rs572715424 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157800005 | CCTAAATATCTCCAC[C/G]TAAGAACTCCATTTT | 51429 |
| rs572722151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157751329 | AATTATCTCCCACTG[A/G]GTCCCTCCCACAACA | 51429 |
| rs572746880 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157929323 | GATAGAAAAATAGTC[C/G]CGTATCCAGCTGTAG | 51429 |
| rs572755543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157814389 | TTGTGTCTTGATTCA[C/T]GCCATCCTTCCTCCT | 51429 |
| rs572779036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157852679 | AACCTCCTGTTTAAG[C/T]GATCCTCCCACTTCT | 51429 |
| rs572785745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157765416 | GCTGGAGTGCAGTGG[C/T]GCGATCTCGGCTCAC | 51429 |
| rs572786833 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157914839 | TTAATGAAGTTCACT[A/G]TATCAGTTTTTTCTT | 51429 |
| rs572796420 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821576 | TTCTCAGAAATTTTC[C/T]AGGAATGTGTCACAT | 51429 |
| rs572820722 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157853534 | CAGACACTTTTTCTG[C/T]CTTCCCCTCCATCAT | 51429 |
| rs572832269 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157807002 | CTTTAATGAGCTACC[C/T]GCATTCCTACCACTA | 51429 |
| rs572847872 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | SNX9 | GRCh38.p7 | 6:157912602 | CCTCCTGCCTGGGAT[C/G]CCCACAGATCATTAT | 51429 |
| rs572873354 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157930620 | TCATAGAAATTTGCA[A/C]CCTATTAAGAGCCAC | 51429 |
| rs572909550 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157727554 | GCTGCCTTAAACTCT[A/C]CCATAAATCTATTCA | 51429 |
| rs572927245 | snp | C/T | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894111 | CTTTTCTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 51429 |
| rs572940571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157829753 | TAATGTTAATGTGAT[C/T]TCACTAGCTTTTGGT | 51429 |
| rs572950217 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157828553 | GGCTGGAGTGCAGTG[A/G]CACGAACACAGCTCA | 51429 |
| rs572956231 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157896663 | TTTGTGCTTTCCTAC[A/G]TGTTTGGAAATTAAA | 51429 |
| rs572968400 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157768406 | CCCTGGGTTTAGCGC[A/G]ATGGCTGTTTTGTCT | 51429 |
| rs572968596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157922013 | TGAGGGGAGTGGAGT[A/G]ACTGATTTTCCCGAT | 51429 |
| rs572979448 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157842095 | TAAATAACTGTAATT[C/G]CTGTTATACTTAAAA | 51429 |
| rs572994640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157733600 | GGCTTGTCCTAGGAG[A/G]CCCCAGCTTCAGCTT | 51429 |
| rs573038359 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157936355 | ACACAGTGAACCCCC[A/C]AAAATTAGCTGGGTG | 51429 |
| rs573049224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157719127 | TGCAGGGTGCCTCTT[A/G]CTCCCAGGATAATGG | 51429 |
| rs573059965 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157856939 | TTGAAAAAAATGATC[G/T]CATTCTATTATTCCT | 51429 |
| rs573061818 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157848709 | GTACTGTGCTGAGCA[G/T]GACTGACAGGGAGCT | 51429 |
| rs573066463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157823479 | CAGGCCGGGCCGGTC[A/G]CTCAGGCCCGGGGCG | 51429 |
| rs573102201 | snp | C/T | 0.000462222 | 0.0151953 | intron-variant | SNX9 | GRCh38.p7 | 6:157896783 | ATTGAGTCATGGTTT[C/T]CAAAAGTCACAAAAA | 51429 |
| rs573113709 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157765836 | TTGGAAACAAGTAGG[A/G]TATGAGTCAGGAAAG | 51429 |
| rs573132828 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157729744 | GGATCACCTGAGTTC[A/T]GTTCGAGACCAGCCA | 51429 |
| rs573141689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157857984 | ATCTGAGGCTGGATA[A/G]TCTTAGGTGGCCTTT | 51429 |
| rs573142050 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157836676 | GCTCACTGCAAACTC[C/G]GCCTCCCAGGTTCAC | 51429 |
| rs573171164 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157727926 | ACAAAAGACCGAAGC[A/C]GGGGTGTCTAATATT | 51429 |
| rs573175606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157856108 | GTATGTTTTATTTTG[A/G]GTGAAGAGACATTTC | 51429 |
| rs573175857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157830260 | TTCCATTGAGAAGGT[A/G]TGTTGTTGGTAAATC | 51429 |
| rs573209118 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157792524 | TACAATGTAGAGTGG[C/G]TAAATGAAACTAACA | 51429 |
| rs573211000 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157763823 | GACTGGCAAATCTAG[A/G]ATCAGCCTCATGACG | 51429 |
| rs573220698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157729059 | CAGTGAGCCGAGATC[A/G]CACCACTGCACTCCA | 51429 |
| rs573242716 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157747595 | TCGAGGCATATTGCA[A/G]TACTGACTCAACATA | 51429 |
| rs573299418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157842655 | GATGGAATCTTAAGG[A/G]GTTGAAGTTAGGTTT | 51429 |
| rs573303997 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157743628 | AGTTCGTTTTGACCA[C/T]TTTTTACAGTGTTCT | 51429 |
| rs573328032 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157793197 | TCAGATGATCCACCC[A/G]CCTCGGCCTCCCAAA | 51429 |
| rs573341743 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157832989 | CAGATCCCAGATATT[A/C]AGTTCAGCAGACATT | 51429 |
| rs573346630 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157859353 | AAGGTGTAGCATGCT[A/C]TATGCCCTGTTCCAT | 51429 |
| rs573353833 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157755043 | TGGCACTTGTAAACT[G/T]TCATGGTGCAGGTGG | 51429 |
| rs573355570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157747130 | CTATGCAGCCTGGTT[C/T]CTAACAGGCCATGGA | 51429 |
| rs573387234 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157816763 | CATGAAGCCCAGCAC[A/T]TCGTTATAATAACTA | 51429 |
| rs573408959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157933209 | TGAAGCAGAAGGATC[A/G]CTTGAGCCCAGGAGG | 51429 |
| rs573414271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157869918 | ACACCTCGCACCCTC[A/G]TACACCTCTCATGCT | 51429 |
| rs573416871 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157839127 | CAGGTTTACTTAAAA[A/T]CGCTGGACTTCATAG | 51429 |
| rs573419994 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157767595 | AGAGATAAATCAAAC[C/G]TCCTTCCCTGAACAT | 51429 |
| rs573431078 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157786614 | AGGTCAATATGTAAC[A/C]ATCAATTGCATTTTT | 51429 |
| rs573436672 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157833178 | ACGTATGTATAAATA[G/T]TTGCCTATTGCATAG | 51429 |
| rs573437694 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157938850 | AGCAGCAGTTAAGTA[A/C]GTGAGACCTTTTAAG | 51429 |
| rs573442928 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157879839 | GCTTCTTTAGAGTAC[C/T]TACTTTTGAGAAATT | 51429 |
| rs573451340 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157741549 | ACACTGCAGTAAACT[G/T]CTGCTGCTGCTGTTA | 51429 |
| rs573479627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157916361 | TTAATGTAGACAATC[A/G]TGTCAGCTTGGAATA | 51429 |
| rs573487077 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157790756 | CAATTGTCCTTGCAT[C/T]CCACACAGCTTTGCC | 51429 |
| rs573499866 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157800875 | CTGTCTGCTCCATTG[A/T]CCATGGAAGCCCACG | 51429 |
| rs573509742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157839643 | TCCCCGTCCTGCTGG[A/G]GAAGCAGACCTATAA | 51429 |
| rs573523030 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157915640 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 51429 |
| rs573526413 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157882337 | TGCTCATTGACAATG[A/C/T]CCCTGGTCACCTAAG | 51429 |
| rs573533961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157877283 | AAGAAAAAAAAAGCG[A/G]GGGGGGCATCTAGTC | 51429 |
| rs573546375 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157722601 | CTCTGTCTTTCCTCG[C/T]CTTAAGGATAGGCAG | 51429 |
| rs573550302 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157777785 | CTGCAGTGGGATTAG[C/G]TGTCACGGCAGCCTC | 51429 |
| rs573569971 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157769548 | GGGAAGACAGAGAGG[A/C]AGGGCGATTCAGGCA | 51429 |
| rs573575433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157826108 | GGTTATCACTGAACT[A/G]TTGGGATTTTTAAAA | 51429 |
| rs573583233 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157726119 | CACCCACAAAGGGGG[-/T]CAAGGTCAAAGGAAC | 51429 |
| rs573584393 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157897631 | CTCACCTCAGCCTCC[-/T]TGAGTAGCTGGAATT | 51429 |
| rs573589311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157738168 | TCCACTTGGTCCAGA[A/G]CTGAGTTCAAGTCCT | 51429 |
| rs573590453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157772378 | GAAGTCTTGCTGGAA[C/T]AGACCCCAAGTGGGC | 51429 |
| rs573592708 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157793362 | CCAAGGACCTTGGCT[C/T]TGGAGACATTCATGC | 51429 |
| rs573596424 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157870287 | TCATGCTCTCACATA[C/T]GCACTCACGTGTGAG | 51429 |
| rs573622956 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157840110 | AGGCTGGTGCTTGGG[C/G]TGTCTTTGGATCTCG | 51429 |
| rs573624293 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, missense, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893323 | GGATGAAACATCTTT[C/G]TCCTGTTAGTATTTG | 51429 |
| rs573647807 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157751234 | ATGCTAAAGTAGAAA[A/C]CCCTGATAAACCCAT | 51429 |
| rs573653160 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157758430 | TCAGAAATATCATTA[C/G]TCTAGCAGCATGGAG | 51429 |
| rs573670766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157879490 | CAGGAACTGAATCAA[A/G]CTCTCTTCATTTTCT | 51429 |
| rs573676617 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157813158 | TTCCTACAAAGAATT[C/T]CTGAAAGTCAAAATT | 51429 |
| rs573685800 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157854215 | TGTCTCCCCACCCCC[A/T]GTGAGCATGCAGTTT | 51429 |
| rs573712044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157913112 | TCCAGACTGGCTTTC[C/T]GGCCAGGAGGTGAAT | 51429 |
| rs573747511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885737 | ATGCCTACAGGGCCC[C/T]ATCCCAAGATAATAA | 51429 |
| rs573748353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157819005 | CCCGTTACTGTTTAC[A/G]GCTCTGTGTCTCCCA | 51429 |
| rs573752673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157867337 | AACCTTCCCTGCCTC[C/T]GGAACAGAACAGGGC | 51429 |
| rs573760852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157757374 | TGGGGCCTTATCCAC[A/G]GCACTCTGTTACCGG | 51429 |
| rs573781025 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157770310 | GGAAGACTTCCTGCT[C/T]GCCAGCCATGGAGAC | 51429 |
| rs573783710 | in-del | -/G | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157826425 | GAATAGCGTGAACCC[-/G]GGAGGCAGAACTTGC | 51429 |
| rs573793797 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157725504 | AGCCTTGAGCTTGGA[A/C]CTGTGGCCCTAAGTG | 51429 |
| rs573805931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157726057 | CACACTCCCTCTCAC[A/G]AGGAGTGGCCAGCAG | 51429 |
| rs573820274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157853567 | TGGGATTTGAATTAC[A/G]TGTATACAGTAACTG | 51429 |
| rs573833483 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157872685 | GCAGAAGCCCTTGAG[G/T]CAAGGTTCTGGATTC | 51429 |
| rs573834823 | snp | C/G | | | intron-variant, nc-transcript-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885230 | CCTCTTTTGGTAATT[C/G]CCAATCAGTAATGTT | 51429 |
| rs573840143 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157765960 | ATCCTTAAAAAAAAT[A/C]TTTTAAAAACAGCTC | 51429 |
| rs573860648 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157928111 | GCTTTTTTCATCTAA[C/T]AGTATATTGTGATCT | 51429 |
| rs573869572 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157774775 | CTCATCTTCTGAAAT[G/T]TGCTCCACCCTCCCC | 51429 |
| rs573887580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157882056 | GAGGGGAAGCCAGTG[C/T]CTGCTTCAAAGTTTC | 51429 |
| rs573887657 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157874305 | CCCTGGCCTCACTCC[A/G]TAGGTCTTATGTTGA | 51429 |
| rs573894066 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157799174 | CTCACTATCATGAGA[A/C]CAGCCTGGGGGAGAC | 51429 |
| rs573896946 | snp | A/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887247 | TTTTGCCCCTTTCCT[A/G]AAACAAATCCTTTGT | 51429 |
| rs573929697 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157764509 | AAATCAGTTTAATTA[C/T]GTCACATTTCCACCT | 51429 |
| rs573951832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157717978 | TTGGAGTCTCCAGTG[C/T]CTATTATTTCCCTCT | 51429 |
| rs573973557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157752878 | AGGCAGAGGTCCCTG[C/T]GGCCTTCCGCAGTGT | 51429 |
| rs573983841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157782290 | GCGTATGCACACTGA[C/T]CTGTTGATAAACTGT | 51429 |
| rs573991419 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157730954 | TTACCTACATTTTCA[A/G]ACTTTTTCTCTAATA | 51429 |
| rs573998812 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157847224 | CCTCCTACCTCAGCC[A/T]CCAAGTTAGCTGAGA | 51429 |
| rs574022234 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157881284 | TAATTGTTTTGAGGC[A/C]CCACAATGGCGAGCT | 51429 |
| rs574030432 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157818838 | CAAACGGTTCCTGTT[A/C]CAGCCTAACACCGCC | 51429 |
| rs574035941 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157945137 | AGAAAAGGTCAGTCT[C/G]GTTGTCAAGCAAGTG | 51429 |
| rs574040008 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157867777 | AAGTTAATCATTCAA[A/C]CCCACATGATTTTTT | 51429 |
| rs574049071 | in-del | -/AAAG | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157893145 | AAACTACATTTCCTT[-/AAAG]AAAACTGTAGAAGGA | 51429 |
| rs574051190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157760475 | GGAGCTCAAGTCTGA[A/G]CCAGAGTGGCCTCTA | 51429 |
| rs574061820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157717463 | CCTCTCTTCCAGCCT[A/G]AGGAGGGAGAAGTAC | 51429 |
| rs574065959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157763947 | CGGCAGTGGAAGAGA[A/G]CAAAGCAGGTGTCAA | 51429 |
| rs574077592 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157857957 | GCGTGGTTCTTGTGG[A/T]CTGGAGAGCCCATCT | 51429 |
| rs574095800 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157805078 | GAGATTTGGAGGCAC[A/G]AGTCATGTAAGCATG | 51429 |
| rs574120984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894277 | ACTACACCTGACTAA[C/T]TTTTGTATTTTTAGT | 51429 |
| rs574133433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157761035 | CACCCTCGTATGAAT[C/T]ACTAGTTACACTTGG | 51429 |
| rs574138575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157783487 | TAAAACATTAACCAC[A/G]GTGGAGCATTGTCAT | 51429 |
| rs574151310 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157793248 | AGCCCACGCACCCAG[C/T]CTTAGAATTACTTTT | 51429 |
| rs574151358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157920605 | AGCATAAACACTTCT[C/T]AGGTGGCCATTCGCC | 51429 |
| rs574166562 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157899943 | TGCCTGTGGGTGTGT[G/T]TGTGGTAAGAGCACC | 51429 |
| rs574207146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157804532 | AGGAAGTAGGCCAAC[A/G]GGATGGAGACCCAGG | 51429 |
| rs574216851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888228 | GGTTCAGAATATTAA[C/T]ATTTTTTTTAACTTG | 51429 |
| rs574243197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157895641 | AAAAAAAAAAAGTAC[C/T]GAGCAAAAATAATAC | 51429 |
| rs574265071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157840807 | TATTATTTTGCATTC[A/G]AGATTTTGTCTGATA | 51429 |
| rs574269261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157786929 | CCCATGAAACATCAT[A/G]ACCTATCCCCAACCC | 51429 |
| rs574291375 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157801737 | GTCTCAAAAAAACTT[-/A]AAAAAAAAAAAAACC | 51429 |
| rs574299358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SNX9, LOC105378078 | GRCh38.p7 | 6:157884696 | TGCCTTCAGAACTGC[A/G]TGAGGCTGTCATTAC | 51429 |
| rs574306661 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888965 | GAGAGAGGGAAAAGA[A/G]GAGGAGAATGAAGAC | 51429 |
| rs574312870 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157864193 | TCCTCCAGGGGTAAG[C/G]GTGTTGTGTCCTGAC | 51429 |
| rs574358827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157942610 | GGGCCCCAGCGCTGC[C/T]GGTGTCATTCGGGGT | 51429 |
| rs574363457 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157800952 | CTATGATCTTGGCCA[G/T]TCTCAGTCACAACAC | 51429 |
| rs574372105 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157891139 | CAGGTTCAAGCGATT[C/T]TCCTGCTTCAGCCTC | 51429 |
| rs574373529 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157836129 | TTGTTTGTTTGTTTG[C/T]TTGTAGAGACAGGGT | 51429 |
| rs574375797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157721612 | GCCTGTGTGCACACT[C/T]TGCAGGGAACCCTCT | 51429 |
| rs574400838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157777248 | AGCCAGGCGCAGTGG[C/T]GGGTGCCTGTAGTCC | 51429 |
| rs574418773 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157872631 | AACCCACATTAATTC[A/G]TATAGCGACTTGGGT | 51429 |
| rs574419664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157850226 | CAGTAAGAAAGCTGC[C/T]GGTATCCTTGGCCAG | 51429 |
| rs574423884 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157755001 | TCCCCTTTTTAGACC[A/T]TGCAGGGTAACTTCC | 51429 |
| rs574427506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157934598 | TTTCACTAAACATGT[A/G]GTCAATATCATGTTG | 51429 |
| rs574437475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157883997 | AGTTATAAATACATC[A/G]AAAGGTACTTTACAA | 51429 |
| rs574446956 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157861753 | CTATGTTTTTTCTAT[A/C]TATGCCTATGACAAA | 51429 |
| rs574474972 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157733262 | AGGCAAGTGGATCAC[A/G]AGGTCAGGAGATCGA | 51429 |
| rs574482377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157780144 | CTGGCTCTCTCCTCC[A/G]CCCTCTCCTAGTTCG | 51429 |
| rs574492113 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157897501 | TCACATAGGCATGAT[C/T]GATTATTGTTATTAT | 51429 |
| rs574509776 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157735414 | GCCCAGACCTGGCCG[A/G]GCGTGGTGGCTCATG | 51429 |
| rs574515039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157911497 | CATGTCAGCACTGCC[A/G]TGGAGTTTGTCCCAC | 51429 |
| rs574532297 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157937232 | AAATTACATGATGTT[G/T]TGTTGTTTTCTTTAC | 51429 |
| rs574549433 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157749276 | GATGGGGTGCAGTCA[C/G]GGTCTGGTTTGGCTC | 51429 |
| rs574556207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157778750 | AAGGAGAGAATTTTT[A/G]CCCAGGTCCAACTGA | 51429 |
| rs574564632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157878195 | TGCATCCAGGTCCCT[A/G]GCCCACTGTGATTGC | 51429 |
| rs574566769 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157787642 | TAGGTTACATCAACA[C/T]TGGTCATTAATATCA | 51429 |
| rs574611868 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157807855 | AGCCAGGGTCCTGGA[A/T]GGAAAAAGATTCCCA | 51429 |
| rs574612144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157924786 | TAATGATATTTTTAA[A/G]AAGATTGGCAAAAGT | 51429 |
| rs574618155 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157816522 | TAGACATGGAAAAGA[A/G]GAGATGAAATACACC | 51429 |
| rs574636633 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157801621 | GTAGTCCCAGCTACT[A/C]AGGGGGCTGAGGTGG | 51429 |
| rs574638426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157837275 | CAATCTCACATTACC[A/G]TGGAGGCTGGTTACT | 51429 |
| rs574660691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157931529 | GTTCTCCAAAGTGAT[C/T]CTGGAATCTTAGCAC | 51429 |
| rs574688018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157891831 | TACAGTATAGTGTGA[A/G]GAACAGCAGAGATGT | 51429 |
| rs574697753 | in-del | -/TT | 0.00517822 | 0.0506191 | intron-variant | SNX9 | GRCh38.p7 | 6:157913545 | ACAGTAAATTCACTC[-/TT]TTTGGTGTACAGTTC | 51429 |
| rs574702050 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157917971 | GTTTTATTATGTTCA[C/G]AGAACATACTTTGCA | 51429 |
| rs574707457 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157811497 | ATTATTGGAGTAGAG[G/T]CTAATTGCTACAAAT | 51429 |
| rs574714353 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157723261 | CTGCGCTCCTTCTAA[C/T]CTCTATTTTCACTGA | 51429 |
| rs574719745 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157718069 | GGCCATTTCACTAAG[A/G]ATAATGGCCCCCAGT | 51429 |
| rs574724687 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157794267 | GCCACCATGTAAGAC[A/G]TGACTTTGCTCCTTC | 51429 |
| rs574727751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157838111 | CCAATTTCCCGGGCT[C/T]GAACAATCTTTCCAC | 51429 |
| rs574735530 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157932676 | TTTGAGACCAGCCTG[A/G]GCAACATGGTGAGAC | 51429 |
| rs574744631 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157825076 | AATATGGTGAAACCC[G/T]GTCTCTACTAAAAAT | 51429 |
| rs574748295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157736951 | TATGTGATGGATTGC[A/G]TTTATTGATTTGCAT | 51429 |
| rs574774431 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, nc-transcript-variant | SNX9, LOC107986663 | GRCh38.p7 | 6:157714458 | GAGAGAACAGGTCCT[C/T]TTCATTCTCTGCCCT | 51429 |
| rs574794576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157937791 | ACCATAGTAGTCTAT[C/T]GTATATTATGATGTA | 51429 |
| rs574839172 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157750613 | CAGACAAATGAGAAT[A/G]CATCCAACTAGAAAG | 51429 |
| rs574860305 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157914021 | AAGAGTAAAATGACT[C/G]GGTCATTTGGCAAGT | 51429 |
| rs574867918 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | SNX9 | GRCh38.p7 | 6:157767404 | AGGATGATGGCAGCA[C/G]CTACCTCATGGGGTC | 51429 |
| rs574871014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157917432 | ATTAAATGCTAAAAA[C/T]TTTCCTCTAAGCATG | 51429 |
| rs574871056 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157791562 | TTTGAAAAGCTGTGC[C/T]CATCCTCCTCAACAA | 51429 |
| rs574896792 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157807035 | CTTTCTTGGCTTCAC[C/T]CTGTGCCTTTCCAAC | 51429 |
| rs574898155 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SNX9 | GRCh38.p7 | 6:157782887 | GAGACTATCTCAAAC[A/G]AACAACAACAAAAAA | 51429 |
| rs574899980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157737390 | GTCTTGGGAGAGTAT[A/G]TGTGTCCAGGAATTT | 51429 |
| rs574908704 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | SNX9 | GRCh38.p7 | 6:157716122 | GCCCACCAGGAATAG[C/T]GGCTATAATGACAAG | 51429 |
| rs574909786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157870821 | CCCCTCAGACACTCT[C/T]ACCTGCTCTCACACA | 51429 |
| rs574941324 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157899539 | GCAGTTTGGGAGGCC[A/G/T]AGGCAGGCGGATCAC | 51429 |
| rs574947356 | snp | C/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888006 | AGTTACCTCTTCTCA[C/G]AAGATGCTGTATTGT | 51429 |
| rs574949041 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157802949 | TTGGGGTGGAGGAGG[C/T]TGGGTTGAAAATTAC | 51429 |
| rs574958671 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157719549 | TGTCTTTTCCTGCCT[C/T]AGTCTCAGTCTTTCC | 51429 |
| rs574984320 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157760982 | AACAAGAAGACTAAT[A/C]AAAATAATTTTGAAA | 51429 |
| rs574989144 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157851734 | AGCTGGGATTACAGG[A/C]GTTCGCTACCACACC | 51429 |
| rs574994455 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157866298 | AAATAAAAATTTCAT[A/T]TAGGGCTGGTCATAG | 51429 |
| rs575014880 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157763042 | TGCATATTTGGGGGT[G/T]GCATATTCTCCTCTT | 51429 |
| rs575041183 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157723966 | CATTCTGCTGATAAC[A/T]TCTGGAGTAAGCACA | 51429 |
| rs575042603 | in-del | -/TAGTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157875760 | TAATTAAAATTTGAC[-/TAGTT]TAGGTGAATTTGTCT | 51429 |
| rs575044934 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157768823 | AGCAGGCGGATCACC[G/T]GAGGTCAAGAGTTTG | 51429 |
| rs575078136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157723203 | CCTGAATTAATAACT[C/T]CTAGAATGAGCATTA | 51429 |
| rs575081408 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157941266 | CGTCACAGCCTCTCT[A/G]TGCCTCTGTGCACCA | 51429 |
| rs575088797 | snp | A/C | 0.00279162 | 0.0372561 | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157715542 | CCATTGCACTCTAGC[A/C]AGGGTGACAGAGTGA | 51429 |
| rs575097706 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157943907 | GCTCCCCATTAGATG[C/G]AAAAGTGTAGGGACT | 51429 |
| rs575103138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157827932 | TACACAGCTTGTCTG[A/G]TTAAATTAAGTGGGT | 51429 |
| rs575118745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157806095 | ACACAAAAATTAATA[A/G]AAGTACGGTTATATC | 51429 |
| rs575119606 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157830224 | GAGATAATTTCCCTT[C/T]CATCTAAAATGAATT | 51429 |
| rs575123725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157775563 | ATGTCCTACCATTGA[C/T]TGACTTTACAGTGCC | 51429 |
| rs575133777 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157852468 | TCACTCTCAGCTTCA[C/G]AATAAGCACGTGTAT | 51429 |
| rs575142502 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157921256 | AAGAAAGTAGCACCT[G/T]GAGGTTGTCATTATT | 51429 |
| rs575160783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157770614 | AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAA | 51429 |
| rs575175518 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157874701 | AAACATACCTCAACA[A/T]GTTTGAAAGAAATCA | 51429 |
| rs575180256 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157813471 | CACAGTTAGCTCTGG[G/T]AGGAGAGGAATTTAC | 51429 |
| rs575194659 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157841975 | CCCGTTTTGTTTCCT[C/G]TAGCCTCCCCTCCCC | 51429 |
| rs575225383 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157762002 | CAGCAGGAAGGGAGC[C/T]GGGCTGGAGCTCTCT | 51429 |
| rs575248580 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157920511 | GTGGGTGGCACACAG[C/G]CAGCAGATGCGGGGG | 51429 |
| rs575249431 | snp | C/T | | | missense | SNX9 | GRCh38.p7 | 6:157896996 | AGGCCTACCAAGGAC[C/T]AGGTGAGGAGAGGGG | 51429 |
| rs575282058 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157874290 | CCCCTATTCACAGGC[C/T]CCTGGCCTCACTCCG | 51429 |
| rs575284890 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157745615 | AGTTGACTTGGAAAG[A/T]TTGGCATTTCCATTC | 51429 |
| rs575287602 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157739325 | AAGAATACATTTATG[C/T]GACCAACAAACATAT | 51429 |
| rs575305357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157867924 | TATCTTCTTCGATAT[A/G]TTTATCTTACAATTT | 51429 |
| rs575325734 | snp | C/G/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890438 | TCTCTATTTGCATTA[C/G/T]GAGGAGAGGATAGCT | 51429 |
| rs575330665 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SNX9 | GRCh38.p7 | 6:157855264 | TATAGTACTCCGTTT[C/T]GCAGAGATCCCATAC | 51429 |
| rs575350411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157841514 | CAGGTTTCCCCCAGG[A/G]AGGTTTAATTGGTTC | 51429 |
| rs575361368 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | SNX9 | GRCh38.p7 | 6:157867713 | GAGAACTGTACATTC[A/G]AGTCTGATTGTCCCA | 51429 |
| rs575361856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157820911 | CGATCTCTTCACCTC[A/G]TGACCCGCCCGCCGC | 51429 |
| rs575366523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157895874 | TGAAACTTGAAGGAA[A/G]CAGATAGGTCCCAAA | 51429 |
| rs575392303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157834581 | GTTGGTCTCAAACTC[C/T]TAGGCTCAAACGATC | 51429 |
| rs575412100 | snp | C/T | 0.00405267 | 0.044832 | intron-variant | SNX9 | GRCh38.p7 | 6:157901854 | CATTTTTATTTTGGT[C/T]TTTTTTTTTTTTTTA | 51429 |
| rs575449086 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157798561 | TTCCTGATTGCGAGG[G/T]CTGTACTGTGGTTAT | 51429 |
| rs575465780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157765349 | GAAATATATTTGTTT[C/T]TTTTTGTTTGTTTGT | 51429 |
| rs575512809 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157836632 | GAGTCTTACTCTCGC[A/C]CAGGCTGGAGTGCAG | 51429 |
| rs575513060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157771122 | AATAAGAAAATAAAT[A/G]ACTAAGAATAACTTA | 51429 |
| rs575515268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157746480 | TTCCATCGCCAGGCA[A/G]AAGACTTCTTTCTGT | 51429 |
| rs575548981 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | SNX9 | GRCh38.p7 | 6:157759857 | AAGTTTGTTTTTTTT[G/T]TTTGTTTGTTTGTTT | 51429 |
| rs575558115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157741144 | TTGAGGCCAGGAGTT[C/T]GAGACCAGCCTGGCC | 51429 |
| rs575561281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157733410 | GCATGAATCCGAGGG[A/G]TGGAGCTTGCAGTGA | 51429 |
| rs575578664 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157816817 | CTACTCCAGTTAATC[A/G]CGGACTCTTCAGAAC | 51429 |
| rs575584451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157922173 | TGCCTGCCCCTGTGG[C/T]CTGTAGTCTGCCAGT | 51429 |
| rs575594992 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157929999 | TTGTATATTGTCTTT[A/G]GCTACATTTGTGTCA | 51429 |
| rs575600893 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157844741 | TGGGACTATAGGCAC[A/C]CGCCACCACGCCCGG | 51429 |
| rs575612661 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157799368 | AATCCTAGCGAAGAG[G/T]ATTAAATCAATTACT | 51429 |
| rs575624939 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157743863 | CTACTGAAAATAAAA[A/G]AAAAATAGCCAGGCT | 51429 |
| rs575625146 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157901459 | GTTTCCTTCTAGGAG[C/T]TGTGTGGTTTCAGGT | 51429 |
| rs575671036 | in-del | -/TTTC | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157924416 | CAGGCACTTGGAAAG[-/TTTC]TTTCACTCTGAGTTT | 51429 |
| rs575673181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157896689 | TTAAAATATTATGTA[C/T]GTAAAATTGTTTTGA | 51429 |
| rs575677312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157838924 | TCCTTTGTGGCCGAG[A/G]ACATAGCGTCTTGGA | 51429 |
| rs575683362 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157943815 | GAAGCGCTGCTGTGG[C/G]CACGGCACACTGCTT | 51429 |
| rs575689515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157810681 | AACCCTTGATGTTGG[A/G]TTTTTTTTTTTTCTG | 51429 |
| rs575692996 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157727867 | AGCTGGCCCAGAAGC[A/G]GGTAGAGATATAGGC | 51429 |
| rs575698520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157791902 | TTAGAAAAAATAATC[C/T]AGCAGAAAGCTAACC | 51429 |
| rs575718530 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157882692 | GCAGATGTGGTAGAA[A/G]TACTAAGAGAACTAG | 51429 |
| rs575738839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157844075 | AGACAGGGTTTCACC[A/G]CTTTGGCCTGGCTGG | 51429 |
| rs575785161 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157760127 | CTGCCCACCTTGGCC[C/T]CCCAAAATGCTGGGA | 51429 |
| rs575786022 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157728127 | GCAAGCTGGGATGAA[A/G]AGATGTTCCATTAGC | 51429 |
| rs575787766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157869837 | TCACGCACTCTCTCA[C/T]ATTATGCATACCCCC | 51429 |
| rs575796469 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157813497 | TTTACAACCCTCAGG[C/G]CTCCATGAGGAAGAC | 51429 |
| rs575818044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157875873 | CTGCTGGGCACAGTA[A/G]CTCACGCCTGTAATC | 51429 |
| rs575820916 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157772315 | CCCAGTACCTGTGAC[A/C]TTATTTGAAAATAGG | 51429 |
| rs575841992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157738043 | TGGTTTGCTGAGGAG[C/T]GTTTTACTTCCAATT | 51429 |
| rs575892263 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157923069 | ACATCAGTTGTGTTG[G/T]TTTTTTTAAATGCCA | 51429 |
| rs575898866 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157777728 | CTGGTGCTGTTGCCA[A/G]CAGGTTGAGCCTAAA | 51429 |
| rs575954553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157749573 | CACCCAGGCTGAAGT[A/G]CAGTGGCATGATCTT | 51429 |
| rs575964506 | in-del | -/CTCT | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157919314 | ATATTTTTTGTCTCA[-/CTCT]CTCTTCTTCCTCTGG | 51429 |
| rs575974165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157785393 | AGTCCTTAACAAGAT[A/G]TTAGCAAACCAAATC | 51429 |
| rs575974187 | in-del | -/A | 0.496245 | 0.0431677 | intron-variant | SNX9 | GRCh38.p7 | 6:157729555 | TAGAATGTAGAATAT[-/A]AAAAAAGATAGAATT | 51429 |
| rs576003841 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157915470 | ACATACAGATTCTGC[A/G]TATATTTTGTTAGAT | 51429 |
| rs576032920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157898855 | CTGGCAGTCATAGAC[A/G]GGAGCTGCCTGTCAG | 51429 |
| rs576057505 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157928324 | ATTTTCCTAAATAAG[A/G]TATTCAAGAAATTAT | 51429 |
| rs576061698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157851896 | GCCCGGCCTGTTTGT[C/T]CTTTTGTGTCTGGCT | 51429 |
| rs576065880 | in-del | -/A | 0.159951 | 0.233219 | intron-variant | SNX9 | GRCh38.p7 | 6:157808077 | AGTGATTTTCTCAGG[-/A]AAAAAAAAAATCCTA | 51429 |
| rs576084821 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157795311 | GTCCCAGCTACTCGA[A/G]AAGCTTAGGCAAGAG | 51429 |
| rs576103620 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157771306 | GGCAAGCTCTTCCAG[A/G]TATTTACAAGGCTAA | 51429 |
| rs576115887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885662 | ATCATCACAGGTGGT[A/G]TGGAAGGATGTGACA | 51429 |
| rs576119331 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157845666 | GGAGTTCAACATGCC[A/C]CATATTTTATACAAA | 51429 |
| rs576157569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157825396 | AATGCAGTTTAGCAA[C/T]TAGTGCAGGTATATA | 51429 |
| rs576190631 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157892131 | AGGGAAAGGTGGAAG[G/T]AAAGGACAGAGAGGC | 51429 |
| rs576239856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888017 | CTCACAAGATGCTGT[A/G]TTGTAGGCCAGTTAG | 51429 |
| rs576264140 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157779389 | AGAGCCTTGGCAAGA[C/T]GCTGTTGGTGGCCGT | 51429 |
| rs576267549 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157831953 | AAAGGTCAAAAAGTT[G/T]TTAAGCATTTTGGTT | 51429 |
| rs576270827 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157754415 | ATAATTTTGCAAAGG[C/T]AGTTTCACTTCTAGG | 51429 |
| rs576272006 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157918942 | ATCCAACAATACATT[A/G]TGGTAATTACTGCTT | 51429 |
| rs576295755 | snp | A/T | | | synonymous-codon | SNX9 | GRCh38.p7 | 6:157909922 | GAACACTAATCGATC[A/T]GTAAACCACAGGTAT | 51429 |
| rs576298181 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157731277 | ATTGCAGATGTGAAC[C/T]ACCGGGCCCAGCCTC | 51429 |
| rs576312869 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894208 | TCCGCCTCCTGGATT[C/G]AAGCAATTCTCCTGC | 51429 |
| rs576322417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157871706 | AATTTTTAAAAATGC[C/T]AGATGTGTATAAGTT | 51429 |
| rs576334614 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157912566 | AGCACAGAAGGGCTC[A/T]ATTTCCCCCTCACTT | 51429 |
| rs576346057 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157944983 | TTTGGTTCTTAGATA[C/T]GTTGATGTTTTGATT | 51429 |
| rs576374306 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887495 | AGACTCTGTATCCTC[C/G]CACCACAGAGACCGC | 51429 |
| rs576375447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157788654 | CTTCACTAAATTTTG[C/T]GACATAAAGTTTTGT | 51429 |
| rs576376187 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894650 | CTATTAAATTACTCA[A/G]AGGAATTATGGGAGA | 51429 |
| rs576379399 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886074 | GCTCATCTCTGCCAC[A/G]CCACAGTTGCTGTTC | 51429 |
| rs576382868 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157872737 | TCTGTTGACCAGCGA[A/G]GTGGCAGAGGGCAGA | 51429 |
| rs576408017 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157803933 | GGCATGATCTTGGCT[C/T]GCTGCAATCTCTGCC | 51429 |
| rs576411059 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157731758 | AAAAATCTATAAAGG[A/G]TATCATTCCCCTCTC | 51429 |
| rs576411669 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157789299 | TATTGCCACAACAGG[C/T]TTAGAAGCAGTATAT | 51429 |
| rs576440529 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157738646 | ATATGGTAAAGATAA[C/T]CCTAAGAAAAAAGAA | 51429 |
| rs576444589 | snp | C/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887799 | TGAGAATAATACCAC[C/T]GCTTATTTCACAGGA | 51429 |
| rs576445232 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157875324 | TGGCATTTCTGTTGG[A/G]TACTAACAAAGAAAT | 51429 |
| rs576447325 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157848789 | CCGTAAAATGATAGG[A/G]GAAGGGTAGTGTTAT | 51429 |
| rs576462958 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | SNX9 | GRCh38.p7 | 6:157766416 | CCCACCTTGCACTGA[C/G]GTGCGTGGAAGTTGG | 51429 |
| rs576474577 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157724894 | ACGATATCATTTTAT[A/G]TCAGGGACGTGAGTA | 51429 |
| rs576498172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157845150 | TTCCGCTCTTGTCGC[C/T]CAGGCTGGAGTGCAA | 51429 |
| rs576526684 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157838257 | GGCTCAAGCAGTCTG[C/T]CCACCTCAGCCTCCC | 51429 |
| rs576530602 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157716872 | GCCATGCTTCCCATG[A/C]CTCTTTTTGGGAAAA | 51429 |
| rs576544692 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157869695 | TGTGGCCAGGTCATT[A/C]CTCGCTGGCAGCATT | 51429 |
| rs576548352 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157847186 | CAGCTCACTGCAGCT[G/T]CCACCTCTTGGGCTC | 51429 |
| rs576553771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157939911 | GCATAGGAGGCATCC[A/G]AGGGAGGCAATGAGG | 51429 |
| rs576562153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157744885 | GAGTAGCTGGGACTA[C/T]AGGTGTGTGCCACCA | 51429 |
| rs576562699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157798332 | GCAACATTCTAGAAA[A/G]TAACTGGTTTGTAAC | 51429 |
| rs576599235 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157927781 | ACCCAGGCTGGAGTG[C/T]AGTGGCACGATCTCC | 51429 |
| rs576604020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157913010 | TTTTTGAATAAAATA[A/G]GGATCACTAAATTTC | 51429 |
| rs576610803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157793215 | TCGGCCTCCCAAAGC[A/G]CTCGGATTACAGGCG | 51429 |
| rs576622081 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157804463 | GACTTGGTGAGTGTA[C/T]CTGTATTAGGGTTTT | 51429 |
| rs576625120 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157752745 | CTTCTACTAATCCTC[C/T]TCAGCACAGACCCTT | 51429 |
| rs576638671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157891103 | GTGGTGTGAACTCGG[C/T]TCACTGCAACCTCCG | 51429 |
| rs576671470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157846285 | TCTTTGGCAGTCTTA[C/T]TTTACCATATCCTTA | 51429 |
| rs576674032 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157936654 | TCTGAGCTGTGGTTT[C/T]CTTATCTGTTAATCT | 51429 |
| rs576725769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157909214 | CGTGAGATAGGTACA[A/G]TACATGAGAATATTT | 51429 |
| rs576744587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157856217 | CCTAAGATTTTCTTT[A/G]GTGTTTTTTATGGTT | 51429 |
| rs576752583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157864376 | GAGTTTTGGAGGGTC[C/T]AAACCCTCTAACCTT | 51429 |
| rs576753724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157833782 | TCAAGAGTTGAATAA[C/T]ATGATTTTACAGTTG | 51429 |
| rs576757254 | in-del | -/TT | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157851444 | CACTATTTCTAGAAC[-/TT]TTTTCACCATCCCAA | 51429 |
| rs576762294 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157838317 | GTGCTCGACCAATAA[-/T]TTTTTTTTTTTTTTA | 51429 |
| rs576765581 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157897796 | GCTGGGATTACAGGT[A/G]TGAGCCACCATGCCT | 51429 |
| rs576794800 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SNX9 | GRCh38.p7 | 6:157728782 | GGGCTTTAAGCAGCC[A/G]TTAAAGATAACACTG | 51429 |
| rs576815783 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157857075 | TTACCAGTTGTCAAA[A/C]TGAATTCATTTCCTA | 51429 |
| rs576822188 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157940399 | TTTACTGGAAAGTAA[C/T]GTTTGTCATTAGCTT | 51429 |
| rs576826125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157734618 | CTTCTTTGTCTTATC[A/G]TTATAGGATTTATGG | 51429 |
| rs576834989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157823636 | GTGCGGCGGGCAGTG[C/T]AGACAGACCACCAGG | 51429 |
| rs576841595 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157777136 | GTGGCTCACGCCTGT[A/C]ATCCCAGCACTTTGG | 51429 |
| rs576842073 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157914400 | ATTTTCTAGAAACAA[A/G]TTCTTTGTTAGATAA | 51429 |
| rs576851572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157917327 | TTTTATCATTTCTAT[C/T]GCTTGGTTTGGGTTT | 51429 |
| rs576856257 | snp | G/T | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893220 | ATGATTGCCTTCATT[G/T]CCAGCGTCCACTGGG | 51429 |
| rs576877331 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SNX9 | GRCh38.p7 | 6:157737154 | TTGATATCAGGATGA[C/T]GCTGGCCTCATAAAA | 51429 |
| rs576894868 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157786177 | CCTCCCGAGTAGCTG[A/G]GATTACAGGCACTTG | 51429 |
| rs576929872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157786872 | TTGCTTTAGTCTAAT[A/G]AATGATCCCCATTCC | 51429 |
| rs576931203 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157755076 | GTGTAGCAGTGAGGA[A/C]GACCAGAGGTCACTC | 51429 |
| rs576933909 | in-del | -/T | 0.00835141 | 0.0640778 | intron-variant | SNX9 | GRCh38.p7 | 6:157917252 | TCATTGTCACCTCTC[-/T]TTTTTTCTTTGGTTT | 51429 |
| rs576934687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157815818 | CCTCATGTTCTCACT[C/T]ATAAGTGGGAGGTGA | 51429 |
| rs576935943 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157941774 | AGTTCTTAAAGGAGA[A/G]CTGTGCTTGATGTAC | 51429 |
| rs576938299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157930030 | TAATGGTAGAGTTGA[A/G]TAGTTTCAACAGAAA | 51429 |
| rs576944928 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157719901 | AGCTAGGCGTGGTGG[C/T]GCGTGCCCATAACTC | 51429 |
| rs576946410 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157801552 | TGGGCAACATGGTGA[A/T]ACCCTGTCTCTACAA | 51429 |
| rs576977493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157883385 | TTATGTCATCTCCTT[A/G]TTTAAGAAACTTCAG | 51429 |
| rs576982358 | snp | A/G | | | intron-variant, downstream-variant-500B | SNX9, LOC105378078 | GRCh38.p7 | 6:157884748 | AGATCCCTGACATCT[A/G]TGAGACAGCTTTGTT | 51429 |
| rs577009894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157836781 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 51429 |
| rs577048506 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822489 | AGAGACCTCGTTTCC[A/G]CTTCAGAGAGCCTGT | 51429 |
| rs577052529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157722967 | AAGATCGTGCCACTG[C/T]ACTCCAGCCTGGGTG | 51429 |
| rs577099181 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157824204 | GCTTGTTTTACGTTA[C/T]TGTTTATGAAATTAG | 51429 |
| rs577110504 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157910907 | CGGGCGGATCACGAG[A/G]TCAGGAGATCGAGAC | 51429 |
| rs577111228 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157800840 | AGCCCCTATTTCACT[C/G]TGTCTCTTTCCAGTC | 51429 |
| rs577138687 | in-del | -/TG | 0.00199481 | 0.0315187 | upstream-variant-2KB, downstream-variant-500B | SNX9, LOC107986663 | GRCh38.p7 | 6:157714990 | GAGGTTGCAGTGAGC[-/TG]CGAGATTGTGCCACT | 51429 |
| rs577140127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157830347 | ACAGCATTTTCTCCT[A/G]GTACAATGAAGGTAT | 51429 |
| rs577155046 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157817463 | AGCAAATGTCCTGTA[C/T]TTGTATTTAGCAAGC | 51429 |
| rs577181762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157919733 | TCAGAGATAGTGTCT[A/G]TTGACTGTTTGTTTT | 51429 |
| rs577185615 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157927754 | TTTTTTGAGACGGAG[G/T]CTTGCTCTGTCACCC | 51429 |
| rs577209032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157736053 | ATAAACTCTAATTTC[C/T]AGAGACACTTGTATT | 51429 |
| rs577213764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157849391 | AGATGTTGAGCACCT[A/G]CTGTGTTCCAGGCAT | 51429 |
| rs577225884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157942569 | GTAGACGCCTCCCGG[C/T]GGGAAGGGACCACCA | 51429 |
| rs577227783 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157827203 | TTTATATAATATATA[A/C]ACATATATTATAGTT | 51429 |
| rs577233278 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157806358 | CTCAAACCCTCCAAA[A/C]TATTTGATCATTGTG | 51429 |
| rs577242479 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157883848 | CACAATTTGTGACTC[G/T]TATACAAATTATATT | 51429 |
| rs577252567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157837182 | TTTAGTTTCTCGCCA[A/G]CTTGTAGTGTTGTCA | 51429 |
| rs577275003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157797731 | AAGGCTCATTGAAGG[A/G]CAGAAACATGTTAAA | 51429 |
| rs577277808 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157773650 | GGAGCTTTGGCTGCC[A/G]TCCAGGGAAGAGATG | 51429 |
| rs577288665 | in-del | -/AC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157818080 | AGGATATATACACAA[-/AC]ACACACACACACACA | 51429 |
| rs577289815 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157785199 | TCAGTGAGCCGAGAT[C/T]GCACCACTGCACTCC | 51429 |
| rs577308183 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157870347 | GCTCACACTCACACT[C/G]ATGCTCTCACACATG | 51429 |
| rs577319746 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157904252 | CAGCCTGGCCAACAT[A/G]GTGAAACCTCAATCT | 51429 |
| rs577328698 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SNX9 | GRCh38.p7 | 6:157764864 | TTGCATCACTGAGCT[A/G]GAAAATTTGCTGGTA | 51429 |
| rs577365547 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157742507 | GAGATGAGATGGGAT[A/G]GGAAGACCTTTGGGT | 51429 |
| rs577369586 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157783251 | TTCAAACTACCTGCC[A/G]CAAAAAATGACAGAG | 51429 |
| rs577403161 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157741278 | ACTGGAACCCAGGAG[A/G]TGGAGCTGCAATGAG | 51429 |
| rs577409088 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157769468 | GCGGAGGAAGGGAAA[C/G]CTCCTGGAGGACAGG | 51429 |
| rs577447452 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157746644 | AGGGGGAGCCTGGCC[A/G]GAAAGAGAGGAAGGA | 51429 |
| rs577448695 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157844305 | GAGTTTTTAAGGACA[A/G]TTTGGTGGGTGGGGG | 51429 |
| rs577452850 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157899391 | TATAAGACTAGATTT[A/G]TCAGTGTCTAGGCCT | 51429 |
| rs577467260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157824293 | GGCGTTTTCAGTAGT[C/T]ACTTGATGTAGAATA | 51429 |
| rs577471044 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157854375 | GCTGTGATAAAGAAC[A/T]AAGTAGCTATGCTGA | 51429 |
| rs577474393 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157742819 | ACACATATGTAACAT[A/G]CACATTACATTACAC | 51429 |
| rs577475477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157772975 | GACGAGAAAGCAGAC[A/G]ACGGGAGCTTCTCCC | 51429 |
| rs577513401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157819685 | AGAATCTAATTTTGA[A/G]TAAAAACACCTGGCC | 51429 |
| rs577513437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157827886 | TTTTTTTAACTCTTC[A/G]GTTCCAATACCTAAA | 51429 |
| rs577515550 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157877437 | AAATATTTTAACTGC[C/T]ATCTCTGCCCTCTGT | 51429 |
| rs577516165 | in-del | -/TT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157744762 | TTTTTTTTTTTTTTT[-/TT]GAGACGGAGTCTTGC | 51429 |
| rs577534357 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157725652 | TCAGGGATGCAGGCC[A/G]CCGAGTGTCAGGGAT | 51429 |
| rs577540040 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157833645 | TAATTTTACCTGCCA[C/G]CATGTGCCTTCTCCC | 51429 |
| rs577549916 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157782463 | TGAAGCATATCAAGC[C/T]GTACAATATTACCTC | 51429 |
| rs577550555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157820204 | ATCCCAGCACTTTGG[A/G]AGGCTGAGGCAGACG | 51429 |
| rs577553849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157880890 | ATCTGTAAAACCTCA[C/T]GGGATTTTTGGAAAA | 51429 |
| rs577558648 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157917119 | AGCTTTGGTAGCTTG[A/G]GTCTTTAAGGGAGTC | 51429 |
| rs577565539 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157870770 | ACACTCACCTGCTCT[C/T]ACACATATATGCACT | 51429 |
| rs577571680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157865110 | TTGGGAAGCCAAGGC[A/G]GGTGGATCACCTGAG | 51429 |
| rs577581093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157847750 | AATCCTGTAACATAT[C/T]TTTCAGTATATTTTA | 51429 |
| rs577630254 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887304 | CATGAAGTTTTCCAT[C/G]TAGGCTGGTGGGAAT | 51429 |
| rs577650753 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157840221 | GTGTCTTTGGATCTC[A/G]GGAAAGAGCAGACCC | 51429 |
| rs577661692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157841457 | GGGAGAGAGAGAGAT[C/T]GAGACCTACCTAGAG | 51429 |
| rs577667763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157940742 | TTCTAACCTCTTAGT[A/G]AAGTGATTTACCAAG | 51429 |
| rs577681027 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157744806 | CTGGAATGCAGTGGC[A/G]TGATCTCTGCTCACT | 51429 |
| rs577695931 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157944056 | ACCAGCACTTCCAGC[A/G]CTTCACTTAACGGCA | 51429 |
| rs577701196 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157873668 | ATATGACACATATAA[C/G]GTATTTTTCCTTTGC | 51429 |
| rs577719167 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157847252 | AGACCACAGGTGTGC[A/G]CCACACTGCTTGGCT | 51429 |
| rs577723462 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157718860 | GTGAGAGTCTCTGCC[A/C]AACTCCTTCTTCCTC | 51429 |
| rs577736669 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157904215 | CCGAGGCAGGCAGAT[C/T]ACGAGGTCAGGAATT | 51429 |
| rs577781684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157907684 | GTTTTAAGTAGAACT[A/G]CACCCATGCACCCAG | 51429 |
| rs577783032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157813228 | CAGTCAGACACCCGA[A/G]GCCTCCCTACAGGAC | 51429 |
| rs577786775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157747016 | ACATGCACAGTTCCC[A/G]ATAGGATTCAAGCTC | 51429 |
| rs577796487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157752149 | TGAGCCGAGATTGCG[C/T]TACTGCACTCTAGTC | 51429 |
| rs577815418 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157732532 | ATTAACACATCCCTC[A/G]CTTCCTACCGTTTCC | 51429 |
| rs577817193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157942474 | GGGCTCTAGGCAAAC[A/G]TGAAGGCCTGAGCCC | 51429 |
| rs577831719 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157774809 | GGCCTGGGGAGAGGG[A/T]GAGAGGGATCACACT | 51429 |
| rs577849809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157913850 | TTTTCGTGGCCAATA[A/G]TATTCCAGTGTTTAG | 51429 |
| rs577850078 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | SNX9 | GRCh38.p7 | 6:157736763 | TGCTTCCAGTTTTTG[C/G/T]GCATTCAGTATGATT | 51429 |
| rs577877520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157775506 | CCAGGAGGCTTGGCC[C/T]ATTTTCCCTTGGTAC | 51429 |
| rs577887261 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157733020 | TTGGCCTGACACCCT[C/G]TAGGTTCATCTGTGT | 51429 |
| rs577892499 | snp | A/C/G | 9.91715e-05 | 0.00704115 | intron-variant | SNX9 | GRCh38.p7 | 6:157940985 | AAACGGTGAGTGGGC[A/C/G]TCCACGTGCCTTTCG | 51429 |
| rs577921334 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157752894 | GGCCTTCCGCAGTGT[C/G]TTGTGTCCCTGGGTA | 51429 |
| rs577925132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157900502 | ATAGACACACACAAG[A/G]TAGCGAAAGCTGGGT | 51429 |
| rs577926052 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SNX9 | GRCh38.p7 | 6:157759688 | AGAGGGAGACCCTGT[C/T]TCCAAATAAATATAG | 51429 |
| rs577945542 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157874986 | GACAATTCTTGCTTG[A/C]CCTCGAAGACTCCCT | 51429 |
| rs577961079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157874231 | CTTTCCCTCAGAAAC[A/G]TGTGCCCATGCACAC | 51429 |
| rs577964709 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157867371 | CACCGTTGGTGTTAT[C/T]CTTCCTCAGAGTAGA | 51429 |
| rs577976059 | in-del | -/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157865353 | GGAAAAAAAAAAAAA[-/G]AAAAAACACCACATA | 51429 |
| rs578001865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157935892 | TTACCAATAAAATCA[A/G]TAATAAAATTTTAAC | 51429 |
| rs578004245 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157770479 | GTAAGCTATTTGCCA[G/T]AAAATACTTTTTAAA | 51429 |
| rs578004724 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157753658 | TCCCCCAGTGTCTAA[C/T]TGGCCAGAACAGGTC | 51429 |
| rs578011637 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157727157 | GATTGTTCCTGGAAC[C/T]GAGCCGGGTCTGGCT | 51429 |
| rs578012198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157867797 | CATGATTTTTTTCCT[A/G]TTGCTTATGAAATAT | 51429 |
| rs578015512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157814139 | TGCCTTCAACTACAT[A/G]AGAGCCTTTTAACTG | 51429 |
| rs578023862 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157882830 | GAGATGGAATCTATT[C/T]GTGGTGAGGATGCTA | 51429 |
| rs578052875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157759071 | CCTGTGCCCTCAGAG[A/G]AGGTTTAAAATCATA | 51429 |
| rs578083254 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157799266 | CGAGATGAAATTTGG[C/G]TGGGGACACAGAGCC | 51429 |
| rs578084735 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157906381 | ACTGAAGATAATTAA[A/C]ACAAATTAATGCCTG | 51429 |
| rs578091249 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157828582 | CACGGCAGTCTCGAC[G/T]TCCCTGGCTCAGGTG | 51429 |
| rs578097426 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157776485 | GGTGGACACTCAGGG[G/T]TGCAGCCCACAGGTC | 51429 |
| rs578110405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157785146 | GCTACTTGGGAGGCC[A/G]AGGCAGGAGAATTGC | 51429 |
| rs578119615 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157816635 | AGGAATGCCACAGGA[G/T]TGAGCAAATACAGGT | 51429 |
| rs578135191 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157901072 | CTGCTTTTCTGGGAT[A/G]GGAATCTTGGTGATG | 51429 |
| rs578135254 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894913 | TAATAGAAAGGAGAG[G/T]TTTATAGGCAGTAAC | 51429 |
| rs578140386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157733940 | GAGAAACTCTCTTCA[A/G]TGTTGTATAAAGACA | 51429 |
| rs578157687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157765313 | ACAGCTATGACTGTG[A/G]GGGCTTCGGGTGTTC | 51429 |
| rs578171475 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SNX9 | GRCh38.p7 | 6:157895721 | ATGGGATGTTTGAGT[A/G]AGTATATACAAGGAA | 51429 |
| rs578177110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157835269 | CCACCTGCCTCGGCC[C/T]CTCAAAGTGCTGGGA | 51429 |
| rs578193353 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SNX9 | GRCh38.p7 | 6:157922104 | CTCTTCTCAGAGCCA[G/T]GCCATTTTCATCACT | 51429 |
| rs578196184 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157764840 | GTGAGAAGATGTACA[C/G]CTCCTGCCTTGCATC | 51429 |
| rs578216453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157882661 | CTCATAGAAGATGTT[C/T]ATGAAGGAAGTAACT | 51429 |
| rs578218839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157784490 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 51429 |
| rs578231433 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SNX9 | GRCh38.p7 | 6:157915351 | AATTTTTATTGAAAC[A/C]GCATTGATTCTGTAG | 51429 |
| rs578251563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157921435 | AGCTTTCTACCCAAT[A/G]GCCAGTAGACATAGA | 51429 |
| rs578260536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SNX9 | GRCh38.p7 | 6:157792399 | CCGCCTTGGCCTCCC[A/G]AAGTGCTGGGATTAC | 51429 |
| rs578261719 | in-del | -/TCTT | 0.00636936 | 0.0560724 | intron-variant | SNX9 | GRCh38.p7 | 6:157744721 | TCCCTCTGGACTTAG[-/TCTT]TCTTTCTTTCTTTCT | 51429 |
| rs745338108 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157758332 | TTTTCTACCATGCCA[A/G]GGAGGCTAGATGTTA | 51429 |
| rs745338997 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157747310 | GCACACACAAACACA[C/G]AAGATATTTTCACTG | 51429 |
| rs745350714 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157759468 | GGGAGGCTGAGGCTG[A/G]TGGATCACTTGAGGT | 51429 |
| rs745363250 | snp | C/T | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893957 | AAGAGAGTCCAGCTA[C/T]AGACCCAAATCTGAT | 51429 |
| rs745369182 | in-del | -/T/TTT | 3.45162e-05 | 0.00415417 | intron-variant | SNX9 | GRCh38.p7 | 6:157901852 | TCATTTTTATTTTGG[-/T/TTT]TCTTTTTTTTTTTTT | 51429 |
| rs745393270 | snp | A/G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157862557 | AACACTGTTGAAGAT[A/G/T]TACTGCTTTTTTCCC | 51429 |
| rs745419601 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157795540 | GTATGATGATAGCAT[C/T]ATGATTATATAAGAA | 51429 |
| rs745462889 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157900545 | CTGCCTTCTGGTCCT[A/G]CAGTGCCAACAATGC | 51429 |
| rs745481618 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157873018 | TTGCTTTTTTTATGT[A/G]TAACAATTCCTCCAC | 51429 |
| rs745503572 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157815586 | TAGGAGCACAAAATG[C/T]GTTTTTCATGACTGA | 51429 |
| rs745518065 | snp | G/T | 3.30797e-05 | 0.00406679 | intron-variant | SNX9 | GRCh38.p7 | 6:157901875 | TTTTTTTTTAACTGA[G/T]GATCTTCCATTTTCA | 51429 |
| rs745518650 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157829109 | TAAAAGTGTATACAG[A/G]TACAACACAAAATTT | 51429 |
| rs745523772 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157770872 | AGTCTCATGCTAAAC[-/A]AAAATTTGCACTGAA | 51429 |
| rs745525711 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157784640 | AAAGTGCTGGGATTA[C/T]ATGCATGAGCCACCA | 51429 |
| rs745536698 | in-del | -/TAAG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157938844 | GATGTGAGCAGCAGT[-/TAAG]TAAGTGAGACCTTTT | 51429 |
| rs745543352 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157801896 | CAACATGATGGGACA[A/C]TTTTTAAAAGATCCC | 51429 |
| rs745551633 | snp | A/G | 2.43353e-05 | 0.00348813 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157928680 | GACGGTGGGGCAGGA[A/G]CACTGGAAGCGCTGC | 51429 |
| rs745566949 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157871488 | AACAATGAGAACACT[C/T]GGACACAGGGCGGGG | 51429 |
| rs745609423 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157724991 | AATTCAGGTCTGCGG[A/G]TGATAAATTCTTTCA | 51429 |
| rs745617840 | snp | C/T | 1.65053e-05 | 0.0028727 | missense | SNX9 | GRCh38.p7 | 6:157937510 | GCTTCCCTGACATCA[C/T]TGGCACTCACAAGGT | 51429 |
| rs745633109 | snp | C/T | 1.64781e-05 | 0.00287033 | missense | SNX9 | GRCh38.p7 | 6:157909666 | GAACATTGGCATAGG[C/T]TGGAGATTATGGCCC | 51429 |
| rs745645550 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157907439 | GGCATGCACCACCAC[A/G]CCTAGCTAATTTTTT | 51429 |
| rs745661462 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157861912 | ACCTGAAGATGAGCA[C/T]TGCCATACCTGATAG | 51429 |
| rs745672864 | in-del | -/GAA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157904425 | GCGACACAGAGACTC[-/GAA]TGTCTCCAAAAAAAA | 51429 |
| rs745696694 | snp | C/T | | | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157715334 | GGTGGATCACATGAG[C/T]TCAGGAGTTCAAGAC | 51429 |
| rs745701371 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157726234 | TGTCTTGAAGTTTAC[A/G]AATCTTTCTTCTGGA | 51429 |
| rs745733813 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157737155 | TGATATCAGGATGAC[A/G]CTGGCCTCATAAAAT | 51429 |
| rs745754061 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157773182 | ATGCTTCCCTTAATC[C/G]TATTTTTTTTAATTA | 51429 |
| rs745758269 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157908454 | ATAATAAGGACTTCT[A/G]TTGCTCTGAAATGTG | 51429 |
| rs745759515 | snp | A/T | 1.65411e-05 | 0.00287581 | missense | SNX9 | GRCh38.p7 | 6:157942791 | TTGCTTTCTTGTCAG[A/T]TTGCAGAAAAGCTGA | 51429 |
| rs745802595 | snp | C/T | 3.29565e-05 | 0.00405921 | intron-variant | SNX9 | GRCh38.p7 | 6:157909825 | AAAGCAGAATCATGT[C/T]TGGATCACTGATTGC | 51429 |
| rs745818885 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157773639 | ATGTCAGTTAGGGAG[A/C]TTTGGCTGCCGTCCA | 51429 |
| rs745821910 | in-del | -/AG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157833527 | TTCCAGGGGAAAAAA[-/AG]AGTATGTTTTAAAAG | 51429 |
| rs745823600 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157737024 | TGATGGTGGATAAGC[C/T]TTTTGATGTGCTGCT | 51429 |
| rs745829311 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157878785 | TTTAAGTAAACAAGT[A/C]ATATTAAATTAGCAA | 51429 |
| rs745836526 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157918755 | TAAATTTTTGAAGTT[A/C]TTTTCATAGTGGTTG | 51429 |
| rs745850667 | snp | C/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890948 | CTGTGCCTGTCTGTA[C/T]CATCCACTTTCAGAA | 51429 |
| rs745857447 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157849966 | GTTGTCAGAGTGGAT[A/G]TTACCCAGGGAGAAT | 51429 |
| rs745858586 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157735639 | ACTGCCTTCAGGTCC[C/T]CTCAGCCTGTGACTG | 51429 |
| rs745881832 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157844407 | TCAGTTCCTGGGTGG[A/G]GGCCACAAGATCAGA | 51429 |
| rs745904014 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157720652 | AGGCAGGCCAAGGGT[G/T]ACGCTGACCCTCTGA | 51429 |
| rs745909026 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157772334 | TTTGAAAATAGGGCC[A/G]GCCTTTGCAGATATC | 51429 |
| rs745924147 | in-del | -/ATT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157935108 | GTGGTGGATTAACTC[-/ATT]ATTTTGAAAACTATA | 51429 |
| rs745937797 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157761692 | AGCTGTTCTGAGCCT[C/T]GGTTTCTCCATTGGT | 51429 |
| rs745957730 | snp | C/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885942 | ATGTTTGGTAGAAAG[C/T]CAAACGGAAAGCAGC | 51429 |
| rs745970434 | in-del | -/TTTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157730202 | ATCTTAGTATAACTG[-/TTTT]TTTTTTTTTAAAAAA | 51429 |
| rs745976060 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157857944 | GTGGACTGACAATGC[A/G]TGGTTCTTGTGGTCT | 51429 |
| rs745985301 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157812838 | TAAGATATTATAAAA[A/G]TAGAGTAATTAAGAC | 51429 |
| rs745990912 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157722171 | AGGTGAAGTGTTTTC[A/G]TGTTTTCTTCCTAAA | 51429 |
| rs745998677 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157937737 | AAAATCTGTACATCA[C/T]CTCAGGCATGAGTTG | 51429 |
| rs746000514 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157762121 | GGGGCCGGGAGGGGC[A/G]GAGTACAAGCTCAGG | 51429 |
| rs746027048 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157876344 | GTAATCCAAGCTGCT[C/T]GGGGGGCTGAAGCAG | 51429 |
| rs746037284 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157939782 | TCCAAATTGAGAAAT[-/A]ACAAAGCTTTGTATA | 51429 |
| rs746064633 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157832818 | GGATTATGGGAACTA[C/T]AATTCAAGATGAGAT | 51429 |
| rs746089788 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157801856 | GTGGCTTCTACCATC[C/T]GAGGCATGTTGTGAA | 51429 |
| rs746099515 | snp | A/G | 2.35924e-05 | 0.00343448 | intron-variant | SNX9 | GRCh38.p7 | 6:157935913 | AAATTTTAACAAGTG[A/G]AAAGAAAATATGCAT | 51429 |
| rs746104512 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157746347 | TATTTATGACACAAC[G/T]TGTTTCCCCTTTAAA | 51429 |
| rs746125658 | snp | G/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887326 | GGTGGGAATAGCCCT[G/T]TGTGAGGGGTTGCAC | 51429 |
| rs746143883 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157858941 | GCAGATTATTACAAT[A/T]CAGGGTGAGATTTGG | 51429 |
| rs746156940 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157754396 | CTCTCTCACTGTCTC[A/G]GTCATAATTTTGCAA | 51429 |
| rs746207729 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157789893 | CCCTCTCATCAGTTA[C/G]GTCTGAGTGACCAGG | 51429 |
| rs746226244 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157778228 | CAGTCTCTGCCTCCA[C/T]CATCACTGTGAATCT | 51429 |
| rs746237743 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157864765 | CCGGGCATGGTGGCT[C/T]ACACCTGTAATCCCA | 51429 |
| rs746248450 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157877123 | TCAAGATAGGTGGAG[A/G]CAGTTTAGCTAATGA | 51429 |
| rs746252442 | in-del | -/AAAG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157923324 | ATGGTAGACACAGAA[-/AAAG]ACCCCCAAAGAATCT | 51429 |
| rs746265514 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157833741 | TTCTCCTCCCGCCTT[C/T]CTAAACCATGACTCA | 51429 |
| rs746272212 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157788560 | TCCCAGCACTTCTAG[A/G]TAGGGGAATGTTAGA | 51429 |
| rs746273511 | snp | C/T | | | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157943197 | ATATAATTTATAAGT[C/T]TCCCACAATCTTCCA | 51429 |
| rs746280883 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157742501 | TGAAATGAGATGAGA[C/T]GGGATGGGAAGACCT | 51429 |
| rs746293665 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157729495 | CTTTATAGTTTTAAG[C/T]TGGGGACTCTCTTGA | 51429 |
| rs746315278 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157927299 | CAGTGTAGCCGCAGC[C/T]GAAACTCAAATCAGA | 51429 |
| rs746377499 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157808394 | CTTTAAGAAATATCC[C/T]AGAGTACAACATAGA | 51429 |
| rs746378824 | snp | C/T | 1.64817e-05 | 0.00287064 | missense | SNX9 | GRCh38.p7 | 6:157921560 | GAATTTATCAAAATG[C/T]GCATGGAGAGACTTC | 51429 |
| rs746388608 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157906644 | AATAGTGTTTTTTCC[A/G]GTAAACCAGCTGTCA | 51429 |
| rs746389216 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157752476 | GTCAGCAGGAAAACA[C/T]GTGGACAAATGTCTC | 51429 |
| rs746402053 | snp | A/T | 1.64768e-05 | 0.00287021 | missense | SNX9 | GRCh38.p7 | 6:157940942 | AGTGTCATCCGCCTG[A/T]ACCTGGAGCAGCAAG | 51429 |
| rs746410399 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157777088 | GTTCTGTTACATAAT[G/T]ACCTTTAAAGGAGGC | 51429 |
| rs746432050 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157852480 | TCACAATAAGCACGT[A/G]TATCTTAGGGCATTT | 51429 |
| rs746445915 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157816758 | ACCACCATGAAGCCC[A/T]GCACATCGTTATAAT | 51429 |
| rs746455232 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157766374 | AAAATGTGTAACTTG[G/T]TGCTCCCCAGACCAT | 51429 |
| rs746464349 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157737198 | AGTCCCTCTTTTTCT[A/G]TTGATTGGAATAGTT | 51429 |
| rs746464397 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157785850 | TGAACTCTGAAATTG[A/C]CTGGAGTCACAGGAC | 51429 |
| rs746470634 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157914554 | CCATCTCAGCTCACT[A/G]CAACCTTGACCTCCC | 51429 |
| rs746472173 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157900936 | CCCTAAAGAGGCCCA[G/T]AAGAGCCCTGGCAAG | 51429 |
| rs746501723 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157773732 | GCGTCTAGATTTCCA[A/G]TACATGCACTTGATG | 51429 |
| rs746501837 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157913663 | CGTGCTGCCCATCCC[C/T]CTGGTCCTAACCATG | 51429 |
| rs746515223 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157881397 | TCTCTGAGACACAAC[C/T]GTATTTCAGTTAACC | 51429 |
| rs746545025 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157858339 | GCAGCCTCCACCACC[C/T]GGGTTCAAGTGATTC | 51429 |
| rs746546760 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157829173 | TTTAAAACATAATCA[A/G]TTTTACTAATGATTA | 51429 |
| rs746570842 | snp | A/T | 1.65075e-05 | 0.00287289 | intron-variant | SNX9 | GRCh38.p7 | 6:157873062 | AGGAAATCTCAACTG[A/T]AATCTTTTTCTTTTT | 51429 |
| rs746580173 | snp | C/G | 1.64768e-05 | 0.00287021 | missense | SNX9 | GRCh38.p7 | 6:157938669 | GAAAGTGACAAACTA[C/G]TTGCAACAAGTAAAA | 51429 |
| rs746583615 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157738210 | TTAACTTTCTGTCTC[A/G]TTGATCTGTCTAATA | 51429 |
| rs746633505 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157863090 | CAGTTAGCCATTGAC[A/G]GCAATACCAGAGAGA | 51429 |
| rs746644079 | in-del | -/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157720240 | GAGTCGCAAATAGAA[-/G]AACCCTAATATCCTA | 51429 |
| rs746686131 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157820539 | TTGATTTTGACTGAC[A/G]TATATAAAAATAAAA | 51429 |
| rs746698378 | snp | C/T | 3.67715e-05 | 0.0042877 | intron-variant | SNX9 | GRCh38.p7 | 6:157902078 | CCAGGGAACCAGGGC[C/T]GTGGTAGAAGTATAC | 51429 |
| rs746719369 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157742096 | TTGGCCTCCAGCAGT[A/G]ATAGCACTGCTAACT | 51429 |
| rs746723147 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157862009 | CTGGACAAAGGGATG[A/G]TTCATGTCCTGAGTG | 51429 |
| rs746738192 | snp | A/G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157811676 | AAGTCGGAGTCAAAG[A/G/T]TGATCCTAAGATTTC | 51429 |
| rs746767736 | snp | C/T | 1.66054e-05 | 0.00288139 | intron-variant | SNX9 | GRCh38.p7 | 6:157932301 | CATTCATCCAGTGGG[C/T]CTTTAGAGCCTTATG | 51429 |
| rs746785678 | snp | C/T | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157892381 | GTCCGAGGGCCGTGA[C/T]GGAAGCTGCAGGAAA | 51429 |
| rs746790981 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157812691 | TAAATGGAAAAGCCT[C/G]GGTCCCTGAATGACT | 51429 |
| rs746791785 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157871400 | AAAAGAAAATCACTG[A/G]GTAGAAAAAGATTAT | 51429 |
| rs746795883 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157879730 | TACTCCTGTGTGTGC[A/T]AGTCTTGTTTTTCAT | 51429 |
| rs746798709 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157780588 | AATTTAAGATAAACA[A/G]TAAATAATATTTTAG | 51429 |
| rs746803652 | in-del | -/ACAT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157818101 | CACACACACACACAC[-/ACAT]ATATATATATACATA | 51429 |
| rs746811985 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157934739 | AATAAATGAAGAAAA[-/C]CCCTAAAGTCATAAA | 51429 |
| rs746826860 | snp | A/T | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893550 | ATTAGGGGCTATATT[A/T]GACAGGGTGGGTAAT | 51429 |
| rs746829547 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157851301 | TATAAATAAACCTCT[A/G]CAAAGTATACAAAAT | 51429 |
| rs746830538 | snp | C/T | | | utr-variant-5-prime | SNX9 | GRCh38.p7 | 6:157716195 | TCAGGCATTTTGTCC[C/T]GGACACAGGTAGGAA | 51429 |
| rs746834425 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157745484 | TAAACTCCCCTGCAG[A/G]CATGGAACCCTTTTC | 51429 |
| rs746847277 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157837555 | TTTTGATGAATTTGA[A/C]TTTCAGCGGCTTCAT | 51429 |
| rs746873368 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157765039 | CCATTACTTTTAATG[A/G]CAAAGATTGCAATTA | 51429 |
| rs746886665 | in-del | -/AA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157735962 | TGAGACTATGTCTCA[-/AA]AAAAAAAAAAAAAAA | 51429 |
| rs746895040 | snp | C/T | 1.64814e-05 | 0.00287061 | intron-variant | SNX9 | GRCh38.p7 | 6:157910037 | ACAGGTGAGTGTGTG[C/T]AATGCTAAACCCAGG | 51429 |
| rs746909411 | in-del | -/TTTTTTTTTT | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894116 | TTTTCTTTTTTTTTT[-/TTTTTTTTTT]TTTTTTTTTTTGAGA | 51429 |
| rs746922093 | snp | A/G | 1.77675e-05 | 0.00298051 | missense | SNX9 | GRCh38.p7 | 6:157936029 | GAAATTGCCAGTCTC[A/G]TGGCAGAACAGGTAC | 51429 |
| rs746925223 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157869475 | ATTTCTGTTGTGGCG[C/T]CTTTCCATTCAGTGA | 51429 |
| rs746928680 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157824199 | GGTTTGCTTGTTTTA[C/T]GTTATTGTTTATGAA | 51429 |
| rs746939001 | snp | A/T | 1.65007e-05 | 0.00287229 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157867573 | GTATGATTTTGCTGC[A/T]GAACCTGGAAATAAT | 51429 |
| rs746957673 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157793493 | TTCCCTCCAACTAGT[A/G]TCTTCTTTTAAGCAT | 51429 |
| rs746964641 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157726380 | TATTTGAACATACAG[A/G]ATACAGGTATTGTGA | 51429 |
| rs746982138 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157880645 | CTAACCGAGTGCCAT[A/C]GTGAGCCACAGTTAT | 51429 |
| rs747026515 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157763522 | ACCCGGAAGCAAGTC[A/G]GGCAGGGAGCCAGGA | 51429 |
| rs747034339 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157928854 | TTCTGCTTGATCTCA[C/T]TTCACCTGAGTTAAA | 51429 |
| rs747041983 | in-del | -/TTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157744744 | TTCTTTCTTTCTTCA[-/TTT]TTTTTTTTTTTTTTT | 51429 |
| rs747050163 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157723477 | AACTGTCACTGTGAA[C/T]TAATAACTTCAGGTC | 51429 |
| rs747076341 | snp | G/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888297 | CTGTATGACTTGCAT[G/T]ATACTTAATCCATTC | 51429 |
| rs747089635 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157730279 | CTGTAATCCCAGCAC[-/T]TTGGGAGGCCGAGGC | 51429 |
| rs747096789 | in-del | -/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886402 | TAACCTTTTATTTTA[-/T]TGTTACAGAAGCAGT | 51429 |
| rs747099467 | snp | G/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889709 | CTTCAATTAAAAGTC[G/T]CTATTAATATGACCT | 51429 |
| rs747102123 | snp | A/G | 1.64991e-05 | 0.00287215 | missense | SNX9 | GRCh38.p7 | 6:157921534 | TGTCGCTTGCAGGCC[A/G]CTTTGAAGAGGAATT | 51429 |
| rs747112419 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157754079 | CCAGCTGATCCATCA[A/C]GTGCAGGGTCTGCAA | 51429 |
| rs747124749 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157803965 | CCTAGGTTCAAGCCA[C/T]TCTCCTGCCTCAGCT | 51429 |
| rs747126957 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157830280 | GTTGGTAAATCTCTT[A/G]TATGTCTCTTAGGTA | 51429 |
| rs747136383 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157846977 | ACTTGAACCTGGGAA[A/G]TGGAGAAGTGAGCCC | 51429 |
| rs747151171 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157909015 | ACGGAAGAAAACAGC[C/T]AGCCTGGTTCTTGCT | 51429 |
| rs747161017 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157865792 | TTAAAATAATTTCAG[G/T]CATCATTAAGCAAAT | 51429 |
| rs747168186 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157772408 | CCCTAGGTCCAATGA[C/T]TGGCATCCCTAGAAG | 51429 |
| rs747185600 | snp | A/G | | | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157944225 | TAATAATTACGGGAA[A/G]TGGAAAGTCTGGGCC | 51429 |
| rs747191157 | snp | G/T | 1.65026e-05 | 0.00287246 | missense | SNX9 | GRCh38.p7 | 6:157896849 | GTGGCAATGACCCCT[G/T]GTCAGCCTGGAGTGC | 51429 |
| rs747192131 | snp | A/G | 1.65081e-05 | 0.00287293 | missense | SNX9 | GRCh38.p7 | 6:157937460 | TCTCCATTTCCTGAT[A/G]GAATGTAATCACGAG | 51429 |
| rs747194950 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157878253 | TTTATCAGCCAAAAC[A/G]CAGTTCAGCTTGGCT | 51429 |
| rs747219291 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157819471 | ATGCCCTAAAGTGAG[A/G]GGAGGTATCCCCTTG | 51429 |
| rs747220561 | snp | A/G | 1.65836e-05 | 0.0028795 | intron-variant | SNX9 | GRCh38.p7 | 6:157875201 | ACTTCCTCCTTCTGG[A/G]TGTGGCTGGCTTTAC | 51429 |
| rs747225396 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157722314 | TTTTGTTATCCTCAT[C/G]TGACAATAAGCCCTC | 51429 |
| rs747275016 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157762282 | CAGTTTTCAAGCGTG[C/T]AGTTCCTTCTATGAA | 51429 |
| rs747282780 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157877206 | TGGTATTTACTTGTA[A/G]TTTAATATAAACTGG | 51429 |
| rs747308310 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157765378 | GTTTGTTTTCTGAGA[C/T]GGAGTCTCGCTCTGT | 51429 |
| rs747317873 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157809936 | CATCCTCTTATCATA[G/T]GATCACTCAATTTCA | 51429 |
| rs747328782 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157819134 | CACTTTTCATACATA[C/T]ATTCAGCTAGTCTAA | 51429 |
| rs747356649 | in-del | -/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157914246 | TTCCTGATGGCGAGT[-/G]GGGTTGAGCATCTCT | 51429 |
| rs747357734 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157901173 | CATTCTGGCAGTCCC[A/T]CCTGGCACTGTCTTT | 51429 |
| rs747377342 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157769729 | GTCTGGAGGCCTGTG[C/T]GGAGGATTTTTGGTG | 51429 |
| rs747393864 | snp | A/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894771 | TGCATTCTCTTTCAA[A/G]AGCAATTTGACAAAA | 51429 |
| rs747418098 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157866861 | TGAGAGTCAGTGTTC[C/G]CAGAATGAACAGTTT | 51429 |
| rs747429162 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157787064 | CTGAGGAAAGCAGAT[A/T]GCCCACCCTGATGCG | 51429 |
| rs747438004 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157759742 | AAGTTTAATGATATA[A/G]ACTTACAAATTGAAT | 51429 |
| rs747438758 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157718573 | GTCTTGAATTAAAAA[A/G]TAAAAGCTAGATTGG | 51429 |
| rs747447683 | in-del | -/AA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157923439 | ATCTAAAAAAAAAAT[-/AA]AACCTGTCATTTACA | 51429 |
| rs747467251 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157871675 | TAGAACTTAAAGTAT[A/T]ATAATAATTTTTAAA | 51429 |
| rs747509478 | snp | C/T | 1.65721e-05 | 0.0028785 | intron-variant | SNX9 | GRCh38.p7 | 6:157938789 | GCTGGTGGAAGTTTT[C/T]TTTTCCCCAGCAAAG | 51429 |
| rs747544094 | in-del | -/TA | 3.38728e-05 | 0.00411524 | intron-variant | SNX9 | GRCh38.p7 | 6:157938587 | TTTTAAACTAATGAC[-/TA]ATCATTTCAGCTTTA | 51429 |
| rs747550521 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157796751 | ATTTGTTGAGTATCT[A/G]TTACACACAGGCACT | 51429 |
| rs747557697 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157805275 | ATCGCTCCATCTCCC[A/G]TGTCTCTCCCCTCTA | 51429 |
| rs747604256 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157726899 | TTGCACATGGATCTG[A/G]TAAAATGTTGTTCTA | 51429 |
| rs747604942 | snp | A/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157891386 | TCTGTGATCGACCAC[A/G]ACAAGTTAATTTTTT | 51429 |
| rs747606216 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157740608 | TAGGTGTCCAGCATT[A/G]GCTGGAGAGCTCTGC | 51429 |
| rs747618282 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157854876 | GTTTGCAACATGACT[C/G]TGAGCATCCTAGGTA | 51429 |
| rs747627488 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157863372 | GCTTTGAATCCACTA[A/G]TGTTTATTTTACTGA | 51429 |
| rs747637871 | snp | A/C | | | utr-variant-5-prime | SNX9 | GRCh38.p7 | 6:157766535 | TACTGGACACTTCTC[A/C]GGTATTACATTTTTC | 51429 |
| rs747645817 | snp | A/G | | | missense | SNX9 | GRCh38.p7 | 6:157932218 | AAGGAATATCAGAAG[A/G]TAGGAAAGGCCTTGC | 51429 |
| rs747648089 | in-del | -/ATAG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157797514 | ATTTTTATTTAAATA[-/ATAG]ATAGATCGATTGTCT | 51429 |
| rs747649271 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157855791 | GGCTGGAGTGGAGTG[C/T]AGTGGCACAGTCTCG | 51429 |
| rs747670308 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157786827 | TGAGCTCTGCACGCT[A/G]TAACAGAGAGGTGCT | 51429 |
| rs747673175 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157776739 | GGCTTGGCTCCCGTA[A/G]GTTTGTTTGCTACAG | 51429 |
| rs747690103 | snp | C/G | 2.12015e-05 | 0.00325581 | intron-variant | SNX9 | GRCh38.p7 | 6:157873056 | TTCTCCAGGAAATCT[C/G]AACTGTAATCTTTTT | 51429 |
| rs747694588 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157832167 | GTAGTATCTGAAAAT[C/T]GAGTCATATGGTATT | 51429 |
| rs747701061 | snp | C/T | 1.70397e-05 | 0.00291883 | intron-variant | SNX9 | GRCh38.p7 | 6:157906113 | AGACTGATGAACATT[C/T]ATATTCATGATTAGA | 51429 |
| rs747726891 | snp | A/G | 1.64789e-05 | 0.0028704 | missense | SNX9 | GRCh38.p7 | 6:157940952 | GCCTGTACCTGGAGC[A/G]GCAAGTGCAATTTTA | 51429 |
| rs747763740 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157751247 | AACCCCTGATAAACC[C/T]ATCAGATCTCGTGAG | 51429 |
| rs747765383 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157852399 | TTCTCAGAATTCACA[A/G]TCCTCCTTTCCATTT | 51429 |
| rs747786458 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157775558 | CCCTCATGTCCTACC[A/G]TTGACTGACTTTACA | 51429 |
| rs747832966 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157825514 | GCATGTGTCTTTGAT[A/T]AAACACGAGCCTTAA | 51429 |
| rs747846254 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157920104 | TCCTGTCCTCTGTCA[A/G]TGTAACTGTAACTCG | 51429 |
| rs747860327 | snp | C/T | 3.3012e-05 | 0.00406262 | missense | SNX9 | GRCh38.p7 | 6:157867557 | GATAGGCTCGGGTTA[C/T]GTATGATTTTGCTGC | 51429 |
| rs747861185 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157746463 | AGGTAATGATCCTGC[A/G]CTTCCATCGCCAGGC | 51429 |
| rs747889558 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157864411 | GTGAGTAAGTGCTTA[C/G]TAATATTTAAGTGTG | 51429 |
| rs747906626 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157882239 | GATGACAGCACATCT[A/G]TTTGCAATATGATTT | 51429 |
| rs747924520 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157782840 | GCAGTGAGCCAAGAT[C/T]GCGGCACTGCAGTCC | 51429 |
| rs747929631 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157836979 | TATTGTGAGGGATGG[A/C]AAAATAAAAGAAAGA | 51429 |
| rs747938094 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157734494 | CCTTCACAACATTAG[C/T]TTCTCAGCTGGGAGG | 51429 |
| rs747942516 | snp | G/T | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157891256 | CTGGTCTCAAACTCC[G/T]GACCTCAAGTGATCC | 51429 |
| rs747957988 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840380 | GGTTTTCACCACACC[C/G]AAAATGACTGACTTT | 51429 |
| rs747986581 | snp | A/G/T | 3.30804e-05 | 0.00406686 | intron-variant | SNX9 | GRCh38.p7 | 6:157875181 | ACAATCACCAGGTAC[A/G/T]TCTCACTTCCTCCTT | 51429 |
| rs747990779 | in-del | -/A | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888229 | GTTCAGAATATTAAC[-/A]TTTTTTTTAACTTGG | 51429 |
| rs748008077 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157747102 | TGCTCACTTGTCCGC[C/T]GCTCACCTCCTGCTA | 51429 |
| rs748021775 | snp | A/G | 1.65034e-05 | 0.00287253 | missense | SNX9 | GRCh38.p7 | 6:157902005 | GCTCAGCGAGGAAAC[A/G]GTCGTGCTAGTTCCT | 51429 |
| rs748033150 | snp | A/C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157781492 | AGGCCTTGGTTCTTA[A/C/T]AAAATTCTCTGGAAA | 51429 |
| rs748046639 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157911751 | TATTCTCCTTAAAAC[A/G]TTACTTTATATTTTA | 51429 |
| rs748051225 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157899543 | TTTGGGAGGCCGAGG[C/T]AGGCGGATCACAAGG | 51429 |
| rs748056605 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157898712 | AGAAGGTAGTCTCCC[A/G]TTATTTTTTAACAAT | 51429 |
| rs748067640 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157775032 | TTCCCAGGGCCGGCT[C/G]TGTTGCTGATCAACA | 51429 |
| rs748071261 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157859226 | TTCCACTTGTGTTAT[C/G]ACTGAGTTTCTTCTC | 51429 |
| rs748071791 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157938350 | TCCTCAAATGGCAGC[A/G]GCTTCTGAATATTAC | 51429 |
| rs748093832 | snp | G/T | 1.6531e-05 | 0.00287493 | intron-variant | SNX9 | GRCh38.p7 | 6:157932281 | TATCAAGGTGCGTCT[G/T]TCTTCATTCATCCAG | 51429 |
| rs748107494 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157837260 | GTCTCAACACTGTTA[C/G]AATCTCACATTACCA | 51429 |
| rs748110242 | snp | A/C | 1.65064e-05 | 0.00287279 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157932196 | TTTTTGTCTTTCAGC[A/C]TTACCCAAGGAATAT | 51429 |
| rs748121556 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157781515 | TCTGGAAAAGGATGA[C/T]TGTGGAGATTAAGTT | 51429 |
| rs748125222 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157938886 | CGTTTGCAGGATCCC[A/G]GTGCTGATGAAAATC | 51429 |
| rs748127616 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157858171 | TTTTCATGCCTATGT[C/T]AGTATCACATATGCT | 51429 |
| rs748127955 | snp | A/G | 1.64958e-05 | 0.00287187 | missense | SNX9 | GRCh38.p7 | 6:157938645 | CAGGGAGCAATAGAA[A/G]AAGTGAAAGAAAGTG | 51429 |
| rs748170669 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157925715 | CCAAAGAACGCATTT[-/A]ATAGGGCTCTTTGCT | 51429 |
| rs748186878 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157755085 | TGAGGACGACCAGAG[G/T]TCACTCTCGTGGCCA | 51429 |
| rs748194641 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157835759 | GAAGGTGCCTTGCTT[-/C]CCCTTCACTTTCCAT | 51429 |
| rs748196099 | snp | A/G | | | downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157945444 | TGTTGCTGTTCCATG[A/G]ATACTGGAAGGGGCC | 51429 |
| rs748211268 | in-del | -/AAAAG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157884437 | TAAAAATAAATTGAT[-/AAAAG]AAACCCTCACAAAGG | 51429 |
| rs748219172 | snp | A/G | 4.94376e-05 | 0.00497156 | intron-variant | SNX9 | GRCh38.p7 | 6:157909872 | CATTTTCTAGAGTTG[A/G]CATTGGTAACCTTTT | 51429 |
| rs748222315 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157824202 | TTGCTTGTTTTACGT[C/T]ATTGTTTATGAAATT | 51429 |
| rs748226409 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157743931 | CTGAGGCAGGAGAAT[C/T]GTTTGAACCCAGGAT | 51429 |
| rs748257241 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157849800 | AGGCAGGGTCTGTGC[C/T]GGAATGCTGATGAGG | 51429 |
| rs748280402 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157835973 | TCACTCTGTTGCTCA[C/G]GGTGGAGTGCCGTGG | 51429 |
| rs748308043 | snp | A/T | | | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821901 | ATAAGTATTACCAAA[A/T]GGGCAAGTTATTTAA | 51429 |
| rs748310533 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157895771 | AAAAATTATAGTAGG[C/T]CATTGTTTCAGAGTT | 51429 |
| rs748327685 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157867905 | ATTATGTCTGCTTAT[G/T]TTGTATCTTCTTCGA | 51429 |
| rs748334695 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157935325 | TTCTAGGTAACGATC[A/G]TTTTCTAACATTCTA | 51429 |
| rs748344576 | in-del | -/TTTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840420 | TACTTTCTTTCTTTC[-/TTTT]CTTTCTTTTCTTTCC | 51429 |
| rs748356683 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157810007 | ACAAAAACACTGGTA[A/T]GCAATGTTCATAGTA | 51429 |
| rs748366807 | snp | G/T | 1.64841e-05 | 0.00287085 | missense | SNX9 | GRCh38.p7 | 6:157875093 | TTTTCTTGTGGAAAT[G/T]CAGTGGCTGACCAAG | 51429 |
| rs748370728 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157912714 | ACTCGATAATTCATG[-/A]AAAAAATGTACAGTT | 51429 |
| rs748387201 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157764715 | AGGAGCGAGGTTGAG[C/G]CAAGCTCTGTGCAGG | 51429 |
| rs748399868 | in-del | -/A | 1.89838e-05 | 0.00308083 | intron-variant | SNX9 | GRCh38.p7 | 6:157936082 | TTAAGATTTGTTGCT[-/A]TCTAGTCCACATATT | 51429 |
| rs748402548 | snp | G/T | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894856 | ATTTCAGAGACCTTT[G/T]GGATTGCAGTTTTCA | 51429 |
| rs748403191 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157769570 | ATTCAGGCAGAGGGG[A/G]TCACCTGTAAGGAGG | 51429 |
| rs748424715 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157849833 | TTGCTTGGTGTGTTG[G/T]GTGCTCTTGGAACTG | 51429 |
| rs748438854 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157896364 | AATAGGTCCTCATGT[C/T]GAGTGGGAAAAAGAA | 51429 |
| rs748462957 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157799219 | CAATCACCTCTCACC[A/G]GGTCCTCCCCTGACA | 51429 |
| rs748473655 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157842847 | TGGAGCCAGAGGCTA[C/T]ATGACCCCGAAATTG | 51429 |
| rs748499092 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157812226 | TCATTAAAAACATTT[A/C]AATAAGTTCAGCTCA | 51429 |
| rs748524521 | in-del | -/AA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157809633 | TTGCTTCTAAATAAT[-/AA]GACAAAAAACCTAAT | 51429 |
| rs748527517 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157925402 | GTGTTGGGGGAAAAT[C/G]GTAAGACTAATTTGG | 51429 |
| rs748551706 | in-del | -/TTTT | | | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821599 | TGTCACATATTTCCT[-/TTTT]TTTTTTTTTTTTACA | 51429 |
| rs748553518 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157720368 | TGCCTCATGCAGCCC[A/G]TGGCTTTGGGAGAGG | 51429 |
| rs748554695 | snp | A/G/T | 4.50788e-05 | 0.00474739 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157928668 | GAAGGAGCTGCTGAC[A/G/T]GTGGGGCAGGAGCAC | 51429 |
| rs748558262 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157856063 | CTGTCATTGATTTTT[A/G]TCTTGTTTATGTTGG | 51429 |
| rs748562874 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157867470 | CAGCATGCTTAGAAA[C/G]TGAACTGTACACCTT | 51429 |
| rs748567579 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157874748 | AGACCACAATGGAAT[C/T]ACACTAGAAATCAAA | 51429 |
| rs748588605 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157918675 | TTCTTTTTCCTCCTT[G/T]ACTGCCTTTTCTTTG | 51429 |
| rs748596376 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157731945 | GCTGGGAATGCCAGT[C/T]AGGGAAGCAGGAGCC | 51429 |
| rs748598927 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157780355 | AAAGGAAGATTTTCC[C/T]TCTGAGCGTCCAGGG | 51429 |
| rs748600684 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157769928 | GCAGCCCCCAGGGCA[C/T]GGCTGGCTTCACGGG | 51429 |
| rs748609127 | snp | C/T | | | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157943272 | AAAACATGAACTATG[C/T]CAGAATAAAAAATAT | 51429 |
| rs748609394 | in-del | -/TTTT | 4.09492e-05 | 0.0045247 | intron-variant | SNX9 | GRCh38.p7 | 6:157901855 | ATTTTTATTTTGGTC[-/TTTT]TTTTTTTTTTAACTG | 51429 |
| rs748647997 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157941560 | CAAAAATCTAGTAGC[A/G]TGTCTCCCTCAGACA | 51429 |
| rs748658409 | snp | A/C | 9.9054e-05 | 0.00703685 | intron-variant | SNX9 | GRCh38.p7 | 6:157937541 | AACCTGATCGTAGAC[A/C]TTTATAGAAGACAAC | 51429 |
| rs748681336 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157913797 | TTTAGCATAACACAT[G/T]TGCAATTCAATCATT | 51429 |
| rs748684403 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157789571 | TACAAACTTTGAGTT[-/A]ATACTGCCTGGATTC | 51429 |
| rs748700961 | snp | A/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885713 | ATGTGGTGATAGGCG[A/G]ACCCCTGAATGCCTA | 51429 |
| rs748702483 | snp | C/T | 1.65023e-05 | 0.00287244 | intron-variant | SNX9 | GRCh38.p7 | 6:157901889 | ATGATCTTCCATTTT[C/T]ACCTCTAGCAACTGG | 51429 |
| rs748719170 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157751193 | AGGCACTTCTTACAT[A/G]GGGGTGGCAAGAGAA | 51429 |
| rs748730940 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157880925 | AATGAAAAAAGAGTT[C/G]TAAAGTATTTAGAAG | 51429 |
| rs748748957 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157728901 | AGTCAGGAGTTCAAG[A/G]CCAGCCCGGCCAACA | 51429 |
| rs748756087 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157807812 | AAAAACTATATTCTC[C/T]CAAGAAAACAACAAT | 51429 |
| rs748756588 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157844287 | CAAATCAGTCTACCC[A/G]TAGAGTTTTTAAGGA | 51429 |
| rs748759925 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157793706 | GCAACCCCAGCACCT[C/T]GCACAATTCTTCATG | 51429 |
| rs748779468 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157898415 | GGAAGCTGAGCCCAC[A/G]TTCTGATCTCCACAT | 51429 |
| rs748785276 | snp | C/T | 1.65627e-05 | 0.00287769 | intron-variant | SNX9 | GRCh38.p7 | 6:157932182 | TAATCGTTTATTCCT[C/T]TTTGTCTTTCAGCAT | 51429 |
| rs748786021 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157819365 | GGTGAGGACGTCATA[C/T]GTTTATTAGGATTGG | 51429 |
| rs748805473 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157768815 | GAGGCTGAAGCAGGC[A/G]GATCACCTGAGGTCA | 51429 |
| rs748810504 | in-del | -/ATTTTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157878431 | ATATGGAAGCCCACC[-/ATTTTT]TTTTTTTTTTTGAGA | 51429 |
| rs748816290 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840422 | TTTCTTTCTTTCTTT[-/C]TCTTTCTTTTCTTTC | 51429 |
| rs748820557 | in-del | -/AG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157923438 | AATCTAAAAAAAAAA[-/AG]TAACCTGTCATTTAC | 51429 |
| rs748849887 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157806553 | CCATCTGTATCCTAC[C/T]GTCTACCAAATAATC | 51429 |
| rs748857048 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157863918 | AAATCCTTTTTTCTC[C/T]AAAATTATTCTCAGT | 51429 |
| rs748873836 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157776858 | GTATGATATTTACGG[A/G]CTATGTGCCTGAGAC | 51429 |
| rs748887370 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157758340 | CATGCCAAGGAGGCT[A/G]GATGTTACATGGAAT | 51429 |
| rs748898433 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157758461 | AATGGATTCGAGAGC[A/G]GCAAGTCTGGGGATA | 51429 |
| rs748898493 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157741847 | TAAAATTACTAAAGC[A/G]TCGCATTTCCGGCGG | 51429 |
| rs748915218 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157767699 | TTCAAATGTACCACA[A/G]TCTCAGTTCATATGA | 51429 |
| rs748920433 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157825557 | GACTTCCTACTTCGT[C/T]ATCTACACCACTCCA | 51429 |
| rs748941318 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157781419 | TATGAGGTCTCAGTC[C/T]ATGCTTATGTAATTT | 51429 |
| rs748952122 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157795387 | CGCCACTGCACTCCA[G/T]CCTGGGCGACAGAGA | 51429 |
| rs748954379 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157769376 | CACCCCCATCTTCGT[A/G]GACAGGAAATACACT | 51429 |
| rs748959574 | in-del | -/T | 0.020831 | 0.0999079 | intron-variant | SNX9 | GRCh38.p7 | 6:157901854 | ATTTTTATTTTGGTC[-/T]TTTTTTTTTTTTTTA | 51429 |
| rs748978706 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157923076 | TTGTGTTGGTTTTTT[A/T]AAATGCCACCTTCAA | 51429 |
| rs748983226 | snp | C/T | 1.64923e-05 | 0.00287156 | stop-gained | SNX9 | GRCh38.p7 | 6:157901996 | GCAGGCGGCGCTCAG[C/T]GAGGAAACAGTCGTG | 51429 |
| rs749014251 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157865303 | CAAATGGCATCACTG[C/T]ACTCCAGCCTGGGCA | 51429 |
| rs749028910 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157815459 | CTGGACTCAAACAAT[A/T]CTCCCAACTCCCAAA | 51429 |
| rs749037346 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157940076 | AGTTCTGACAGCGTC[A/G]CTGGTGCTCAGGGGC | 51429 |
| rs749040365 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157735694 | ACCTGAGGGCCTGGC[A/G]CAGTGGTTCACACCT | 51429 |
| rs749076408 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157723638 | CAGAAACTGCTGAAG[C/T]GTGGCAAGCTTGTCT | 51429 |
| rs749092516 | in-del | -/AAA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157735961 | GTGAGACTATGTCTC[-/AAA]AAAAAAAAAAAAAAA | 51429 |
| rs749106926 | in-del | -/CATT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157830812 | AAATTGCCTTTTCTC[-/CATT]CTTTCTTTCTGGAAC | 51429 |
| rs749115773 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157828243 | AGTCAAAGATAAGTT[C/T]TGTGACAGTAGAAAG | 51429 |
| rs749145471 | in-del | -/TTTAAA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157835010 | AAAAAGTATAGACAT[-/TTTAAA]TTTAATTTTATTTTT | 51429 |
| rs749147814 | snp | C/T | 1.71773e-05 | 0.00293059 | intron-variant | SNX9 | GRCh38.p7 | 6:157873213 | TTCATTAGAGCTCAT[C/T]TTTGCCAGGCATCTT | 51429 |
| rs749148592 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157763607 | GTGGAACCCCTCCTC[C/T]TCCATGAGTCACCCG | 51429 |
| rs749203434 | snp | C/G | 4.94727e-05 | 0.00497332 | missense | SNX9 | GRCh38.p7 | 6:157875075 | AGTGATGGAAAAGAT[C/G]AATTTTCTTGTGGAA | 51429 |
| rs749206356 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157848534 | TGGGGCAGTAAACCT[A/G]GATGAAGTGAAGTTT | 51429 |
| rs749232087 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157928948 | ATTAGTTCCAGTAAT[C/T]TGGGGCTTTATAATC | 51429 |
| rs749243239 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157747257 | AACAGAACGGAAGGG[A/G]CCAGAGGGACCTGGA | 51429 |
| rs749292182 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157860547 | ATGGTACATGTGATA[G/T]GGCCAGTTGATGCCA | 51429 |
| rs749294581 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157900493 | TGAGAAATAATAGAC[A/G]CACACAAGATAGCGA | 51429 |
| rs749298058 | in-del | -/C | | | upstream-variant-2KB | SNX9 | GRCh38.p7 | 6:157715541 | GCCATTGCACTCTAG[-/C]CAGGGTGACAGAGTG | 51429 |
| rs749326244 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157745340 | GTGGCAGTGATCGTC[A/G]TCGTAATAGCCACGT | 51429 |
| rs749339624 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157732131 | AGAGCCTGGAGGCAG[A/G]GAGGGCGGCCCCTTA | 51429 |
| rs749355892 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157769488 | TGGAGGACAGGGGAT[A/G]TTGTGCTGAAGTCAA | 51429 |
| rs749361166 | in-del | -/CA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157904304 | AGCTGGGCGTGGTGG[-/CA]CGCCTGTAATCCTAG | 51429 |
| rs749370653 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157820955 | GCTGGGATTACAGGC[A/G]TGAGCCACAGCGCCC | 51429 |
| rs749389830 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157868234 | TTTTATTCAAACAAG[A/G]AGCAACTCTATGTAT | 51429 |
| rs749393595 | in-del | -/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157941812 | ATATTTGTGAATTGT[-/G]TCTTGGACAGTTGGT | 51429 |
| rs749413435 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157838581 | AGTAAAAATAAATGT[A/G]TATCAATAAAGAGCC | 51429 |
| rs749415039 | snp | A/G | | | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822037 | GCAAGCAGGCCGTCA[A/G]TGAATGTTGGCCTCC | 51429 |
| rs749428287 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157919811 | TTTTTTGTTGAAAAC[C/T]GGACATTTTTGAGAA | 51429 |
| rs749431019 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157789653 | ATCATTGTGCTTCAG[C/T]TTCCTTATCCACAAA | 51429 |
| rs749445990 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157760510 | AATCAGTCTGGTGAG[A/G]CTGGTATAGCAGAGC | 51429 |
| rs749448018 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157771578 | GAACTGGTTTTGATT[C/T]TCAGAAGAGAAGAGG | 51429 |
| rs749454043 | in-del | -/TG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157787464 | CTCTCTGTGTATATG[-/TG]TGTGTGTGTGTGTGT | 51429 |
| rs749478159 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157925583 | AGTAGAATAGATAAA[G/T]AAATTGGGGATTACT | 51429 |
| rs749497560 | snp | A/C | 0.000115375 | 0.00759437 | intron-variant | SNX9 | GRCh38.p7 | 6:157909840 | TTGGATCACTGATTG[A/C]AGCTTGCTTTTTTCT | 51429 |
| rs749498343 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157897563 | CCCAGGCTGGAGTGC[A/C]GTGGCACAATCTCGG | 51429 |
| rs749509132 | snp | A/C | | | upstream-variant-2KB, nc-transcript-variant | SNX9, LOC107986663 | GRCh38.p7 | 6:157714557 | ATTTATCCCTTGTGT[A/C]TACACTGATGGATGT | 51429 |
| rs749527723 | snp | A/G | | | missense | SNX9 | GRCh38.p7 | 6:157937492 | ATAAAGGTTTTCTTG[A/G]CTGCTTCCCTGACAT | 51429 |
| rs749528078 | snp | A/G | 3.30202e-05 | 0.00406313 | intron-variant | SNX9 | GRCh38.p7 | 6:157937535 | CAAGGTAACCTGATC[A/G]TAGACATTTATAGAA | 51429 |
| rs749528786 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157743729 | TATTTTAATCATAAA[-/T]TAAGGCCAGGCATGG | 51429 |
| rs749537029 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157787763 | ATAAAGTAGATTTCA[C/T]TAATAGCTAATTATC | 51429 |
| rs749560150 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157869909 | CATGCGCACACACCT[C/T]GCACCCTCATACACC | 51429 |
| rs749566797 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157856203 | TTTTTAGAAATTCTC[C/G]TAAGATTTTCTTTGG | 51429 |
| rs749587311 | in-del | -/C | 7.47692e-05 | 0.00611384 | intron-variant | SNX9 | GRCh38.p7 | 6:157873075 | GTAATCTTTTTCTTT[-/C]TTTTTTTTTTTTTGG | 51429 |
| rs749608538 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157721847 | TAGCACCTTCCACAG[C/T]GCCTGGCCACGTAGA | 51429 |
| rs749612941 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157786945 | ACCTATCCCCAACCC[A/G]TGTATCAATTTGGGC | 51429 |
| rs749623824 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157884085 | TTCTTAACACCGACC[A/G]CAGGCCTAGGAGCTG | 51429 |
| rs749625328 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157751433 | CTCAAAAAATTAAAA[C/T]TAGAACTACTATATA | 51429 |
| rs749633361 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157914860 | GTTTTTTCTTTCATG[A/G]ACTGTGCTTGAGGTG | 51429 |
| rs749637373 | snp | C/T | 3.30028e-05 | 0.00406205 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157942865 | CCTTGAAGAGAATGC[C/T]GCGTGCTTTCTCCTG | 51429 |
| rs749640103 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157830628 | ATGATGTTCTACATC[C/T]GTGCCGTCCATATGG | 51429 |
| rs749640843 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157775875 | AGAGTCATGTTTGAG[G/T]AGTGTGGAGACAGTT | 51429 |
| rs749654427 | snp | A/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887027 | TCTTCATTATGGGTC[A/G]TATTTTCCTTGCTTC | 51429 |
| rs749661773 | snp | A/C/T | 0.00011579 | 0.00760809 | intron-variant | SNX9 | GRCh38.p7 | 6:157875180 | AACAATCACCAGGTA[A/C/T]GTCTCACTTCCTCCT | 51429 |
| rs749670479 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157913873 | GTGTTTAGATATACC[A/G]TAGCTTGTTTATCCA | 51429 |
| rs749671284 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157845492 | CATTTCTTGGAAACA[A/G]TTACTCTTTTTTGAA | 51429 |
| rs749672171 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157752305 | CACAGAGACAAAGTA[C/T]AGAGAAAGAAAAGTG | 51429 |
| rs749709796 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157740766 | AGCCTCTCCCGCACC[A/G]GCTCAGGGCTGCCCC | 51429 |
| rs749717412 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157906032 | TGCACCCGAAAGACA[A/G]GACAAGGTTAAAACT | 51429 |
| rs749720063 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157926548 | GAACTTTTGGAGGCT[A/G]AGGTGGGCAGATTGC | 51429 |
| rs749726354 | snp | A/C | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157892741 | TTCCTGGCCAGTTTG[A/C]TAAGACTGAACTGTC | 51429 |
| rs749774619 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157750748 | TATATAAGAGACTTC[C/T]ACAACTCAACAGAAA | 51429 |
| rs749776605 | snp | A/G | 6.60012e-05 | 0.00574423 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157942866 | CTTGAAGAGAATGCC[A/G]CGTGCTTTCTCCTGA | 51429 |
| rs749791437 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157818779 | GTCCTTCTGGGAGTC[A/G]GAACTACCCAAACTC | 51429 |
| rs749815669 | snp | G/T | 1.68332e-05 | 0.00290109 | intron-variant | SNX9 | GRCh38.p7 | 6:157927242 | GCCAGGTTTTCTTTC[G/T]TCTCAATCCGCACCC | 51429 |
| rs749819753 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157823906 | GGGTGGGGGTCGAGA[A/C]CTCGGCGGAGAGGAC | 51429 |
| rs749825009 | snp | A/G | 3.30551e-05 | 0.00406528 | stop-gained | SNX9 | GRCh38.p7 | 6:157896901 | AAGCTCAGAAGGCTG[A/G]GGGGCCCAGCCAGAG | 51429 |
| rs749827313 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157761631 | CGGCCTAGAAGCAAG[C/T]TCTGGTGCACGTGAA | 51429 |
| rs749890136 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157908911 | AAAGAATGGAGGCCT[A/G]CCCTCTTCAGGCAAG | 51429 |
| rs749890480 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157855797 | AGTGGAGTGCAGTGG[C/G]ACAGTCTCGGCTCAC | 51429 |
| rs749898879 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157744873 | CCTCAGCCTCCCGAG[C/T]AGCTGGGACTACAGG | 51429 |
| rs749911997 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157935718 | TCATCTATTAGGCAA[A/G]ATTTATGAATGAGAT | 51429 |
| rs749934102 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157741118 | TTGGGAGGCTGAGAC[-/A]GGGGGATTGCTTGAG | 51429 |
| rs749939805 | in-del | -/AGT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157841081 | AGTCTTGAGAGCAGC[-/AGT]AGAAGAAAGCAGCTG | 51429 |
| rs749949034 | snp | A/G | 1.64985e-05 | 0.0028721 | intron-variant | SNX9 | GRCh38.p7 | 6:157910077 | AGAAAGACTCCAGTC[A/G]GATTATCTTCCTGTA | 51429 |
| rs749978491 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157854629 | TTTAGAAACTGTTCC[C/T]TTTTAACTTCATTGT | 51429 |
| rs749992890 | in-del | -/GG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840057 | GATCTGAGGGAAGGT[-/GG]GGGGGTGTCTTTGGA | 51429 |
| rs749993497 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157760122 | GTGATCTGCCCACCT[C/T]GGCCTCCCAAAATGC | 51429 |
| rs749995079 | snp | A/C/G | 3.30138e-05 | 0.00406276 | missense | SNX9 | GRCh38.p7 | 6:157875063 | CAGATTTTACCCAGT[A/C/G]ATGGAAAAGATCAAT | 51429 |
| rs749998260 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157803104 | GACTAACTTGTCTTT[C/T]GTGTGTGCATGTAGC | 51429 |
| rs750001985 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157935123 | ATTATTTTGAAAACT[A/C]TAAAGAGAAAGAATT | 51429 |
| rs750012181 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157726991 | GAGGTCACTCTAGTT[C/T]GGAGGTGAGGCTTCA | 51429 |
| rs750031969 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157925890 | ACGGAGGCTGGAAGT[A/C]GAAGATCAAGGCACC | 51429 |
| rs750033298 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157843318 | ACTTTCGACTCCCCC[A/G]AAACTTAACTACTAA | 51429 |
| rs750051216 | in-del | -/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157753771 | GGTTCACCTTGCCCC[-/G]CTGCCTAGACAGAGC | 51429 |
| rs750073691 | snp | A/G | 0.000148452 | 0.00861418 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157875155 | TCAGGCCAGTTCGTC[A/G]GCTGCCAGCAACAAT | 51429 |
| rs750083926 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157825798 | CCAGAGAGTCAAGTT[G/T]GTGCTTTCCTCCCTT | 51429 |
| rs750092725 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157743312 | TGGTGACAGTACCAT[C/T]TAATGGGCCAGACAT | 51429 |
| rs750096275 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157769638 | GGAGAAAGCCACAGT[A/G]GACACACCAAGGCCG | 51429 |
| rs750109929 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157779964 | TTTCGTTTACTAACA[A/G]TGGGGCTGTTCGGAA | 51429 |
| rs750111213 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157798537 | TGACTGTACTTCACC[A/G]ATGTTAATTTCCTGA | 51429 |
| rs750139762 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157883851 | AATTTGTGACTCTTA[C/T]ACAAATTATATTGCT | 51429 |
| rs750156307 | in-del | -/TG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157771485 | CATTTATAATATATA[-/TG]TCGTAATTATTCAAT | 51429 |
| rs750179923 | in-del | -/TT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157871775 | TCTTCAGTCTTACCT[-/TT]TTTTTTTTTTTTTTT | 51429 |
| rs750181261 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157751031 | AATACAAAATGGTGC[A/G]GCCACTATGGAACAT | 51429 |
| rs750181450 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157941987 | ATTACATTTGTCTGT[A/G]TGAGAAAATAATGCA | 51429 |
| rs750183113 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157831350 | TGGGGACATTACATC[C/T]TTGGAGTCACTATAT | 51429 |
| rs750211028 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157899957 | TGTGTGGTAAGAGCA[C/T]CTAAAATCTCCCTCA | 51429 |
| rs750222720 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157830032 | GAATTACAAAAAGAC[A/G]TAAGGTTATTTAACT | 51429 |
| rs750227437 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157921795 | ACAGTGAGGGGACAG[A/C]AACCTAAATCCCCAC | 51429 |
| rs750230437 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157914201 | TCCGATAGGTATGCA[A/G]TGGTATCTCAGCATG | 51429 |
| rs750246930 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157799600 | TGGGAAGAAAAAGAC[A/G]TTTAATTGGACTTAC | 51429 |
| rs750266029 | in-del | -/AT | 1.66096e-05 | 0.00288176 | intron-variant | SNX9 | GRCh38.p7 | 6:157942754 | GTCGTAATGGGAGTG[-/AT]ATATCTCAACGTTGT | 51429 |
| rs750275049 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157845234 | CTGCCTCAGCTTTCC[A/G]AATAGCTGGGCTTAC | 51429 |
| rs750325155 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157919664 | AAAATCCTTATAGAA[C/T]CTGCTTTATCTGCCA | 51429 |
| rs750330990 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157750176 | TAAAAGACCCTGAAT[A/G]CCCCAATCTATCTTG | 51429 |
| rs750355150 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157850995 | GCGTGGTGGCTCATG[A/C]CTGTAATCCCAGCAC | 51429 |
| rs750364376 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157818388 | AGATTAAGGGTGGGT[C/T]TGCCTTCCCCAACCC | 51429 |
| rs750368096 | snp | A/G | 1.67548e-05 | 0.00289432 | intron-variant | SNX9 | GRCh38.p7 | 6:157938607 | ATTTCAGCTTTATTC[A/G]TACTGTTGCATTTTA | 51429 |
| rs750377609 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157931025 | CTGATCAACTCCATG[G/T]CCTGTGTAATTCACA | 51429 |
| rs750390920 | in-del | -/TTTC | 0.000117099 | 0.00765087 | intron-variant | SNX9 | GRCh38.p7 | 6:157927234 | GAGACGCTGCCAGGT[-/TTTC]TTTCTTCTCAATCCG | 51429 |
| rs750411633 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157787861 | CGTGTTTTCATGAGA[C/T]CTTAATATCCCCTGC | 51429 |
| rs750416848 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157747018 | ATGCACAGTTCCCGA[C/T]AGGATTCAAGCTCCC | 51429 |
| rs750420968 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157827714 | AAAGGGGACATGAAG[A/G]AAATTGTTAGTGGAG | 51429 |
| rs750429419 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157875673 | CACTTGGTACTCTTA[A/T]TGTATTGCTTCCAGG | 51429 |
| rs750434594 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157783135 | ATATTACTTTTGGAG[A/G]AAATAGATAGCAAGA | 51429 |
| rs750438363 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157903270 | AAAAATTAAAAACAT[A/T]ACATTTGACATATAT | 51429 |
| rs750443096 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157863005 | GTCCTTCAAACAGGA[C/T]ACTGTTTCTCTTTGT | 51429 |
| rs750451815 | in-del | -/ATTTAAAGAGCTCCT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157838727 | TTAGTTTGAGGTCTC[-/ATTTAAAGAGCTCCT]ATTTTAGTGACTGAC | 51429 |
| rs750500608 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157910673 | TTTGGTAAGTAACCC[A/G]TAGTGTTACTAGAGC | 51429 |
| rs750510233 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157841068 | CTGAAGCCCCAGCAG[C/T]CTTGAGAGCAGCAGT | 51429 |
| rs750511678 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157810443 | CACTGAATTGTATTA[C/T]AAATTACTCCCTAAT | 51429 |
| rs750526641 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157809134 | TAACTTAATATTAAC[C/T]AAAAATGTTCAAGAT | 51429 |
| rs750581095 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157772781 | AGAAAACTAGGTTAA[A/G]GCACATTGAGCCCAA | 51429 |
| rs750602780 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157900162 | TAGATTTTTTTAAAG[A/T]CCTGTTAAAAGTTCC | 51429 |
| rs750604039 | snp | C/G | 6.14546e-05 | 0.00554288 | intron-variant | SNX9 | GRCh38.p7 | 6:157897042 | TGCCCGCCCATGGCT[C/G]AGTGGGAGAGACAGG | 51429 |
| rs750606748 | in-del | -/ACAA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157786462 | AAAAGGAAATAAAAG[-/ACAA]ACAGATTGGGAAAAG | 51429 |
| rs750612382 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157757829 | GGGGCTAGGGCTGGC[A/G]TCGGGTGGAGGGATT | 51429 |
| rs750619619 | snp | A/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888051 | CTAAGAGCACACACC[A/G]GGAGACATTGTGTTC | 51429 |
| rs750630682 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157913847 | TTCTTTTCGTGGCCA[A/G]TAGTATTCCAGTGTT | 51429 |
| rs750657670 | in-del | -/CTTC/CTTTCTTTCTTG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157780736 | TTTCTTTCTTTCTTT[-/CTTC/CTTTCTTTCTTG]CTCTCTCTCTCTCTT | 51429 |
| rs750658214 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157939898 | TTGGGAGAAGGCGGC[A/T]TAGGAGGCATCCGAG | 51429 |
| rs750667872 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157784170 | AGCAAGCAGAAGAAA[C/T]GTCAGAATTCAATGA | 51429 |
| rs750671944 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157782769 | GCATGTGCCTGTAAT[A/C]CCAGCTATTCGGGAG | 51429 |
| rs750677362 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157815239 | TTTTTTTTAGACAGC[A/G]TATCACTCTGTTGCC | 51429 |
| rs750690221 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157911410 | ATTCTCACTGCACTC[A/G]CAAGAGTCGAGAGAA | 51429 |
| rs750694452 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157899510 | TTATCTATATTTTCA[C/T]GCCTGTAATCCCAGC | 51429 |
| rs750695731 | snp | A/G | 2.1642e-05 | 0.00328946 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157928635 | GGGGAAGTTCACCAA[A/G]GCCATGGATGACGGC | 51429 |
| rs750697401 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157849351 | GCCATGCTTATTAAC[A/G]TTGGGGTTTATTTAG | 51429 |
| rs750716909 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157724650 | AGAAAAAAACACCTT[G/T]ACTAATCAGACCATT | 51429 |
| rs750718155 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157722462 | GCCACAGGATGCTAC[A/G]CCCTCTAGAATTATT | 51429 |
| rs750736334 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157932492 | TTCTTGCTAGCTCGT[C/T]TGCCTTTTTTTGCTC | 51429 |
| rs750766688 | snp | C/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889845 | TTATTCTTTTCTTTA[C/T]ATTTTAGATGAGCCC | 51429 |
| rs750773511 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157753894 | CAGTCTCCCTGATCA[C/T]TGGGGAGCAGAGTTT | 51429 |
| rs750779856 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157803710 | ATCGAAGAGTCTGTA[A/T]GGAAAAGTGTTTAAA | 51429 |
| rs750787499 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157861594 | TTCTGTATTTAGTTC[A/G]CATAACAGTGGAGTA | 51429 |
| rs750789716 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157917393 | CTTAGATTATTGTTT[C/T]GAGATATTTCCGCTA | 51429 |
| rs750807669 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157940449 | GTTTGAGACAGTCTC[A/G]CTCTGTCACCCAGGC | 51429 |
| rs750815017 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157849057 | TTTGAGGCTGCAGTA[A/G]GCTGTGATGCACCAC | 51429 |
| rs750818838 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157848089 | ACTCACCACCACCTG[G/T]AATTGCTTTGCGTGT | 51429 |
| rs750863686 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157754909 | CTCCATAGACAGAGC[A/C]GCCCCGAGGGCTGCT | 51429 |
| rs750873608 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157928763 | AGGCTCAGTTTTATG[G/T]CCCTTATCATAGAGG | 51429 |
| rs750874108 | snp | G/T | 1.74595e-05 | 0.00295456 | missense | SNX9 | GRCh38.p7 | 6:157873108 | ACTTATTAGGATGTA[G/T]GTGGAGGATGGCTGG | 51429 |
| rs750891525 | snp | A/G | 3.32757e-05 | 0.00407881 | intron-variant | SNX9 | GRCh38.p7 | 6:157942743 | GAACACTGTGAGGTC[A/G]TAATGGGAGTGATAT | 51429 |
| rs750905795 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157773387 | CATGTCCAGAGGCAC[A/G]TGGAAGAAGTCTGCA | 51429 |
| rs750911872 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157790953 | TCCATTAAAATCCTG[G/T]GGTCTGGCTCCTAAC | 51429 |
| rs750913325 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157879170 | TGAGTTCCTCCTGCA[C/G]ATCTGCTCGCAGAAC | 51429 |
| rs750919195 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157723111 | TAAAATTCAGCACCT[A/G]AAAATATCCATCTCT | 51429 |
| rs750925471 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157836965 | ACTTCCAGAACCACT[A/G]TTGTGAGGGATGGAA | 51429 |
| rs750926209 | snp | C/T | 0.000247095 | 0.0111124 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157909763 | GTATGGTCTAAAGAG[C/T]TACATCGAATATCAG | 51429 |
| rs750927478 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157736433 | TGTGAATGGGAGTTC[A/G]CTCATGATTTGGCTC | 51429 |
| rs750939699 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157944890 | AATAAGAGAATCCAC[A/G]GGATTTGATGCCTGG | 51429 |
| rs750940908 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157870854 | CCCACACTCTCCTGC[C/T]CTCACACAGATGCAG | 51429 |
| rs750946039 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157722335 | ATAAGCCCTCTAACC[-/A]CCATTTCTTTTGCAA | 51429 |
| rs750951242 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157877961 | CTCTTTGAATAACTT[A/G]TTTCGAGCCTGCTAC | 51429 |
| rs750952570 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157763396 | AGACACAGGTCCCTG[C/T]GGGGAAGTACCTGCT | 51429 |
| rs750972008 | in-del | -/CAGA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157870237 | GCACACACATCCCCT[-/CAGA]CACTCTCACCTGCTC | 51429 |
| rs750978066 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157734740 | TACAGCGCATGTCAG[C/T]AGACTTCGCTGGTTT | 51429 |
| rs750988401 | snp | A/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894535 | GATGGTGGGGGCAGG[A/G]CTAATAGGTGCTAAG | 51429 |
| rs750993388 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157918342 | TGTAGTGACCTCTTA[C/T]ATCATGAGGTGTCCC | 51429 |
| rs751032026 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157761335 | TTATTTTGGGGGAAT[C/T]GGAGGCATGTCTTGT | 51429 |
| rs751034051 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157813443 | TAGAGGGTGTGGGGG[C/T]GGCAGCTCAGTGCAC | 51429 |
| rs751038034 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157940450 | TTTGAGACAGTCTCG[C/T]TCTGTCACCCAGGCT | 51429 |
| rs751042407 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157926198 | TAAGAGAGAGATTAC[C/T]GGTTACCTTTGTGGG | 51429 |
| rs751045815 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157733404 | AGAAGGGCATGAATC[C/T]GAGGGGTGGAGCTTG | 51429 |
| rs751045882 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157845325 | CATGTTGGCCATGCT[A/G]TTCTCAAACTCCTGA | 51429 |
| rs751059352 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157825439 | TATTTCATAGTTAAT[C/T]CTGAACTTAATTTTT | 51429 |
| rs751084051 | snp | A/C/T | 3.38274e-05 | 0.00411251 | intron-variant | SNX9 | GRCh38.p7 | 6:157938587 | TTTTAAACTAATGAC[A/C/T]AATCATTTCAGCTTT | 51429 |
| rs751091337 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157747890 | CTGAGTAATTAATAG[A/T]TGTTACCAATGTTAA | 51429 |
| rs751100183 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157856933 | TGGGGATTGAAAAAA[A/G]TGATCTCATTCTATT | 51429 |
| rs751102803 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157903511 | GTTTCAGAGTCAAAT[C/T]TGAAGTTTTCAGTCA | 51429 |
| rs751108498 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157770533 | TGGCTCACGCTTGTA[A/G]TCCCAGCACTTTGGG | 51429 |
| rs751119737 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157812094 | ATATCCTCATGACAT[A/G]GTAGCTAGTAATCAG | 51429 |
| rs751130440 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157936944 | ATGTGTACACACACT[A/C]ATGTGGTTGTGGGCT | 51429 |
| rs751168440 | snp | A/G | 1.64781e-05 | 0.00287033 | intron-variant | SNX9 | GRCh38.p7 | 6:157909801 | CTACTGTAAGTATCC[A/G]CGTTATCAAAAGCAG | 51429 |
| rs751172920 | in-del | -/TCTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157740117 | AATAATAATAATAAA[-/TCTT]TATTTAACCAATGTT | 51429 |
| rs751182549 | in-del | -/TA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157837384 | GATTTATTTGCATTG[-/TA]TAATATGTTCCTACC | 51429 |
| rs751188745 | snp | A/G | 0.000233329 | 0.0107986 | intron-variant | SNX9 | GRCh38.p7 | 6:157875032 | TATGAAAATAATTGC[A/G]GCTCTTTCTCCTATT | 51429 |
| rs751190384 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157914455 | GCTGTGGCTTGGCTT[G/T]TCATTTTCTTTTTCT | 51429 |
| rs751207824 | snp | C/G | 9.89821e-05 | 0.00703429 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157942848 | ATGTAGGACAGAACG[C/G]GCCTTGAAGAGAATG | 51429 |
| rs751216472 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157837183 | TAGTTTCTCGCCAAC[-/T]TTGTAGTGTTGTCAG | 51429 |
| rs751222385 | in-del | -/TATGTGTG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157734217 | ACTCAGTTTAGGATT[-/TATGTGTG]TGTGTGTGTGTGTGT | 51429 |
| rs751233625 | snp | C/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886617 | AAATGTTATTCCTTC[C/T]ACGCTTAGCTGGTTT | 51429 |
| rs751241964 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157846067 | TGCTGTGCAGGTGTC[G/T]CTTACGGCCCTCCTG | 51429 |
| rs751270991 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157848603 | CTGAACTAGTAAGAT[G/T]GAATTTATTTGGAAA | 51429 |
| rs751275002 | snp | G/T | 4.94319e-05 | 0.00497127 | intron-variant | SNX9 | GRCh38.p7 | 6:157909897 | CCTTTTCTCTTTCCC[G/T]TATTTTGTAGAACAC | 51429 |
| rs751291520 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157865153 | AGACCAGCCTGACCA[A/C]CATGGTGAAACCCTG | 51429 |
| rs751298843 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157895215 | GTTTGTGCACAGCCT[C/T]AGCGAGCTGCTGAAA | 51429 |
| rs751298902 | in-del | -/GC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157841549 | GGTCACACTGTGACT[-/GC]GCACAGCCCATGTGG | 51429 |
| rs751308999 | in-del | -/GA | 1.64925e-05 | 0.00287158 | frameshift-variant | SNX9 | GRCh38.p7 | 6:157927123 | AGGAATGGAAAACTG[-/GA]GAAAGAGGAAGGCCG | 51429 |
| rs751322666 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157819154 | AGCTAGTCTAATGCC[A/G]AGGGGAAACCTTATA | 51429 |
| rs751357326 | snp | G/T | | | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157944245 | AAGTCTGGGCCAGCA[G/T]CAATAAAATGACACC | 51429 |
| rs751357882 | snp | C/G | 1.66396e-05 | 0.00288436 | missense | SNX9 | GRCh38.p7 | 6:157896955 | AAACACTCCCAACAA[C/G]TGGGACACTGCCTTC | 51429 |
| rs751359552 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157919410 | TTCTCTGTGTTCTTC[A/G]TGTTAGTTAACTTCT | 51429 |
| rs751368626 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157767529 | TATCGCGAACCTTCC[A/G]TGTGTTTTTCCTCAA | 51429 |
| rs751368799 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157777757 | AAGGACTTGAAAGGC[A/C]CTGCTGCTGCACCTG | 51429 |
| rs751381803 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157864281 | TTGATCCCCTCTTGA[A/G]GACAAAGCCTCCGTG | 51429 |
| rs751389396 | in-del | -/AATC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157939434 | AAGGGAGTAAAAAAA[-/AATC]AATCCTCAAGGGAGA | 51429 |
| rs751397998 | in-del | -/CATA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157818102 | ACACACACACACACA[-/CATA]TATATATATACATAT | 51429 |
| rs751399035 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157922719 | TGGGAATTAGACAAC[A/T]TGGAGATGCTTCACC | 51429 |
| rs751403112 | snp | A/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894184 | GCGTGATCTCAGCTC[A/G]TTGCAATCTCCGCCT | 51429 |
| rs751432174 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157782892 | TATCTCAAACAAACA[A/G]CAACAAAAAAAGAAG | 51429 |
| rs751463005 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157942714 | ATGTTTAACTTGTTG[A/G]AGTTGTGAATAAAGA | 51429 |
| rs751483827 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157728717 | CTAGAAGGGACCTCT[A/G]TTATCTCCCCCAGTG | 51429 |
| rs751487777 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157852786 | TCCACGGTGCCCTGG[C/T]TGGTCTTAAATTCCT | 51429 |
| rs751498457 | snp | C/T | 1.65061e-05 | 0.00287277 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157937472 | GATGGAATGTAATCA[C/T]GAGTATAAAGGTTTT | 51429 |
| rs751533879 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157858701 | GAAAAGAGATTTAAT[A/G]GACTCACAATTCCAC | 51429 |
| rs751549736 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157921010 | GTTACTCTTCATAAT[A/G]CTAAATTTAAACTTG | 51429 |
| rs751565882 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157862274 | TCAGGGTCTGTGAAA[G/T]TAAGTTCTGTTTCTT | 51429 |
| rs751569621 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157785078 | GGTGAAACCCTGTCT[C/T]TACTACAAATACAAA | 51429 |
| rs751611760 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157829796 | GATATATAAAAGCCA[A/G]TAGCTGAATTTTACC | 51429 |
| rs751619378 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157940709 | GGTGTGAGCCACTGC[A/G]CCCAGCTCAACTTGT | 51429 |
| rs751622045 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157724836 | GGAGCTTGAATAAAC[A/T]TTCTTTAAACTAGAT | 51429 |
| rs751646062 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157912491 | AAAGCAGCAGCCCCT[C/T]GGTGTGAAGAAAGTT | 51429 |
| rs751650378 | snp | A/G | | | missense | SNX9 | GRCh38.p7 | 6:157867622 | GGAGAAATCATCACA[A/G]TCACAAATCCGGTAA | 51429 |
| rs751669627 | in-del | -/CCTCTGA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157721646 | CCACCGCGGCTCTCT[-/CCTCTGA]CCTCCCGTCCACTCC | 51429 |
| rs751677321 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157930658 | AGCTTGTGAGCCCTT[A/G]TGAGAATCTAATGCC | 51429 |
| rs751689431 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157856990 | TTGTAAAAGAGAAAC[-/T]TTTATCTACTACTTG | 51429 |
| rs751690245 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157937682 | TGACATTGGTTTGGG[C/G]TGTCCTCACATATGA | 51429 |
| rs751705090 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157784346 | GGATATCACTTCAGA[C/T]CTTATAGTTATCAAA | 51429 |
| rs751723706 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157798572 | GAGGGCTGTACTGTG[G/T]TTATTTAGGAGAATG | 51429 |
| rs751742376 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157918466 | ATATCTTTTCCCATC[C/T]GTTTACTTTCAGTAT | 51429 |
| rs751755136 | in-del | -/CT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157730590 | AACCATCCATTAGCC[-/CT]CTCTACCTAGAGGTA | 51429 |
| rs751776700 | in-del | -/AGGGGAGGAAGGAGAAGGAGGAGAGCCCAC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157899050 | TCAGGCCGTTAGAGT[lengthTooLong]AGGGGAGGAAGGAGA | 51429 |
| rs751786199 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157935639 | TCCCTGAGAGGCCTC[A/G]TTATAGCCGAATGAC | 51429 |
| rs751803620 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157719533 | ACATTTGGCTCAGGC[A/G]TGTCTTTTCCTGCCT | 51429 |
| rs751812274 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157838270 | TGCCCACCTCAGCCT[C/G]CCAAAGTGCTAGGGT | 51429 |
| rs751823191 | snp | A/G | 1.64912e-05 | 0.00287147 | missense | SNX9 | GRCh38.p7 | 6:157927180 | ATATTTTCCACCATG[A/G]AACCAGAGGCACCTG | 51429 |
| rs751826460 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157755653 | ATGGCTTGAAAGGAG[G/T]TGTTTTGCATCTTAA | 51429 |
| rs751834201 | snp | A/G | 1.71455e-05 | 0.00292787 | intron-variant | SNX9 | GRCh38.p7 | 6:157921705 | AGAATATTGAGAGTT[A/G]TCTCATTCACACCAA | 51429 |
| rs751839516 | snp | C/T | 3.31691e-05 | 0.00407228 | intron-variant | SNX9 | GRCh38.p7 | 6:157940998 | GCGTCCACGTGCCTT[C/T]CGCATGTGCTTGAGG | 51429 |
| rs751844551 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157901585 | TCCCAGCACGACTTA[C/G]TAAAGAGACTGCCCT | 51429 |
| rs751846327 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157796265 | TGGTGTTTGGACTAT[C/T]AGTAAGGAGTATAGC | 51429 |
| rs751854029 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157870391 | TGTGAGTGCATGTAC[C/T]CCTCAGACACTGTCA | 51429 |
| rs751885492 | in-del | -/TT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157895235 | GCTGCTGAAACTGGC[-/TT]TTTAAGGCCTGCAGT | 51429 |
| rs751894117 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157861685 | CGGGGGATATGTTCC[A/G]AGACCTCCAGGGATG | 51429 |
| rs751912860 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157744975 | GTCTCGATCTCTTGA[A/C]CTTGTGATCCACCCA | 51429 |
| rs751926946 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157743479 | ATCAAAGACCCAGTG[C/T]GTAATCAAAACAACA | 51429 |
| rs751933500 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157770557 | CTTTGGGAGGCCAAG[A/G]CGGGCAGATCACGAG | 51429 |
| rs751938072 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157879229 | CGGCATTGTTTGTAA[C/T]AGCAGAAAACCGGAA | 51429 |
| rs751944219 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157869552 | CCTAGAGTTTTACTC[C/T]GTCCAGCCTCTTCTC | 51429 |
| rs751973413 | snp | A/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157892684 | GGACACTTGCTATGA[A/G]TAGTTCACCTCCAGG | 51429 |
| rs751993180 | snp | A/G | 1.6743e-05 | 0.0028933 | intron-variant | SNX9 | GRCh38.p7 | 6:157867508 | TTTACTACTCTGTTT[A/G]TGTTTGTAACATCCT | 51429 |
| rs752028062 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157781169 | CCATTCATGTTTTTC[A/C]AGGTCAAAAAAAAAA | 51429 |
| rs752055871 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157755894 | GACAGAAAGTTCAGA[C/T]GCTACGGAAAGACAG | 51429 |
| rs752058970 | snp | A/G | | | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822612 | CCGTCCCGTCCCAGG[A/G]GCTTCAAGCCAGGAC | 51429 |
| rs752063947 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157810008 | CAAAAACACTGGTAT[A/G]CAATGTTCATAGTAA | 51429 |
| rs752067146 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157765712 | TAATTTTCCAGAGAG[A/C]GAGGACCTGGCATAG | 51429 |
| rs752072153 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157897061 | GGGAGAGACAGGGAA[A/G]ACCGAACTGTTTTTG | 51429 |
| rs752074718 | snp | C/T | | | missense | SNX9 | GRCh38.p7 | 6:157867632 | TCACAATCACAAATC[C/T]GGTAAGAGAACTGTA | 51429 |
| rs752114356 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157880197 | GTGTAAGAATTGTGG[C/T]TTTGGCATAAGACCT | 51429 |
| rs752117058 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157808116 | AGCTCATAAACAAAA[A/G]CTATAAACTGCAGGA | 51429 |
| rs752124559 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | SNX9, LOC107986663 | GRCh38.p7 | 6:157714244 | ATCCCAAATGACCAC[A/G]GATGTCTGCTTCCTG | 51429 |
| rs752169763 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157802298 | GAACAGCTTCAGGGT[A/G]TCACCTCTGGGACCA | 51429 |
| rs752171595 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157788373 | GATCATAAATCATTG[A/G]GCTAAGGCATCAACA | 51429 |
| rs752189103 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157753377 | AAAAGAAGTTCACAG[A/G]TAGAGCAGTTTCAGG | 51429 |
| rs752203923 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157752160 | TGCGTTACTGCACTC[C/T]AGTCTGGGTGACAGA | 51429 |
| rs752239003 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157768152 | GTCTCACCATCCACG[C/T]TAACCCCCGCCTAAC | 51429 |
| rs752248122 | snp | C/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893292 | AAGCTGTGTGTTTGA[C/G]AAGTCACAGTCTTGT | 51429 |
| rs752252727 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157876094 | TTTAACTACATAAAA[G/T]GTTTTAAATTCTATC | 51429 |
| rs752258414 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157865229 | CTGTAGTCCCAGCTA[C/G]TTGGGAGGCTGAGGC | 51429 |
| rs752279381 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157846312 | CTTAAGCCTACATTT[G/T]TGCTGCATTAAAAGC | 51429 |
| rs752307846 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157814391 | GTGTCTTGATTCATG[A/C]CATCCTTCCTCCTTG | 51429 |
| rs752308680 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157723314 | TTTTAAGCCACCTCT[-/A]AAACTCTTTTAAAAG | 51429 |
| rs752331774 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157909772 | AAAGAGCTACATCGA[A/G]TATCAGCTAACACCT | 51429 |
| rs752342432 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157869241 | CATTCCACCTTCAGC[A/C]CATTTCTTTACACTA | 51429 |
| rs752356302 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157922988 | TTGATAGATTTTCCA[A/G]GGATTTGATTTAGAA | 51429 |
| rs752396332 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157916957 | CCTCCTTGTTTATAT[A/T]CTGGAAGAGATTATA | 51429 |
| rs752420956 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157841435 | CTTGAAGGTCAGGAA[C/T]TGTGAAGGGAGAGAG | 51429 |
| rs752420959 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157730025 | GGGTGTGGGGGCGGG[G/T]AGTTGGGGCTGAGAG | 51429 |
| rs752421697 | snp | C/T | 1.65329e-05 | 0.0028751 | intron-variant | SNX9 | GRCh38.p7 | 6:157909615 | CACATCAATTGTATT[C/T]ATTATTTTTCCATGT | 51429 |
| rs752421788 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157916087 | TCGCCCAGGCTGGAG[G/T]GCAGTGGCGCTATCT | 51429 |
| rs752427546 | snp | A/G | 3.30366e-05 | 0.00406413 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157937436 | TATCTTGTTATAGCC[A/G]AAGAAAGATCTCCAT | 51429 |
| rs752437635 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157732432 | TAAGGTATACTTGAC[A/G]ATTGGAAATCATATA | 51429 |
| rs752444349 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157725031 | TCTTCAACAAAGTTT[A/T]GCATTCATTTCTGAA | 51429 |
| rs752471298 | in-del | -/AA | | | upstream-variant-2KB, downstream-variant-500B | SNX9, LOC107986663 | GRCh38.p7 | 6:157715045 | AGACTCCGTCTCTTA[-/AA]AAAAAAAAAAAAAGA | 51429 |
| rs752487164 | snp | A/G | 1.68457e-05 | 0.00290216 | intron-variant | SNX9 | GRCh38.p7 | 6:157921680 | GGACATTGTGTTAAT[A/G]TGGCATCAGAGAATA | 51429 |
| rs752505532 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157922943 | GTTTGTTGCCTTCCT[A/G]GTTCCCACAAGACTT | 51429 |
| rs752510884 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157852867 | CATGAGCCACTGTGC[C/T]TGGCCTTTGTATTTT | 51429 |
| rs752515065 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157859482 | CTGGTTTATTTAATC[A/C]GTTGCCTGTTAGTAG | 51429 |
| rs752575147 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157771710 | GGTAGGCAATTTTTT[G/T]TTTTTTTAAGATGGA | 51429 |
| rs752576117 | snp | A/G | 1.65378e-05 | 0.00287552 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157896931 | GGGGGCTGGAGCCCA[A/G]AGAAACACAAACACT | 51429 |
| rs752593075 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157820128 | AAGAGAGATATGCAT[A/G]GTTGATCAAGTGGGA | 51429 |
| rs752599504 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157933526 | CTCATTGCCCTGGCC[C/T]TACCATGTCTTACAG | 51429 |
| rs752600098 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157944677 | CAGTTCCGTAGGTCA[A/G]TGTTGCGGTCCGGGA | 51429 |
| rs752612266 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157933623 | GCATCTTGGCCCAGG[-/T]AACAAGTGGGTGATG | 51429 |
| rs752617177 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157728741 | CCCAGTGCCCACTGG[C/T]GTCCTAGGAAAGCAC | 51429 |
| rs752629953 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157801416 | CTTTTATTTCTATAC[A/C]TAGAGGGGACATTAC | 51429 |
| rs752664990 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157725961 | GCTGCCACAGGCCTG[A/C]ACAGAGCCTGCTCCC | 51429 |
| rs752673699 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157722640 | TGAATCGGAGCTCGC[G/T]TAAAGCAGAAGATGA | 51429 |
| rs752694589 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157778956 | AGCCGATGAGCTGGA[C/T]AGGTAGGTCAGAACC | 51429 |
| rs752701554 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157923972 | CCAGGCTGGGTGTGG[C/T]GGATCACTTGAGGTC | 51429 |
| rs752710183 | snp | C/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890785 | TATGTCGATTTTGTT[C/T]GTTGCATTTTCCAAT | 51429 |
| rs752737769 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157766197 | CCAGCTCTCTGGTAA[C/T]TCTGGTCCCCCATTT | 51429 |
| rs752740983 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157862809 | TCTTATGGCCAGTGT[C/T]TTTTTAAATTAGAAT | 51429 |
| rs752743247 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157883128 | TCAAAACAAGACCCC[C/T]CCGCCACCCCAGCAA | 51429 |
| rs752746077 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157795882 | AAAAATATCTTTGAC[A/G]TAGAGGTGCAAAGCT | 51429 |
| rs752754520 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157850732 | GGTGACTGTATTTAA[A/T]ATATTTTATTTTTCC | 51429 |
| rs752754943 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | SNX9, LOC107986663 | GRCh38.p7 | 6:157714494 | ATCTGCCAACATCTC[A/G]TAAATCCAGGCTCAC | 51429 |
| rs752765319 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157802288 | TCTGTGTATGGAACA[A/G]CTTCAGGGTGTCACC | 51429 |
| rs752765855 | in-del | -/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157729876 | TGACCTATGCTACAA[-/G]GTGGATAAGACTCAC | 51429 |
| rs752795824 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157920546 | AGGAGCAGCCTCCCA[C/T]CACCACAGATTTCCA | 51429 |
| rs752819733 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157817310 | GGATGCCTGATGCCA[C/T]GACCAAGGCCATCTC | 51429 |
| rs752833681 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157941911 | CTCTTTAAATGCACA[C/G]TTTTCCCGTCAGTTG | 51429 |
| rs752833967 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157929913 | CAGTAAACCATGGTC[C/T]GAGCACCATATTTGG | 51429 |
| rs752846674 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157876227 | GAGGCCGAGGCGGGC[A/G]GATCACCTGAGTTCA | 51429 |
| rs752847043 | snp | A/G | 1.64757e-05 | 0.00287012 | missense | SNX9 | GRCh38.p7 | 6:157940904 | TGAATCACTTTCACA[A/G]TAACCGGATCTATGA | 51429 |
| rs752863005 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157834347 | GCTAATTTAAAAGAA[-/T]TTTTTTTTTTTTTTG | 51429 |
| rs752870560 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157793457 | TGTACCAACTTCTTC[A/C]CTCCAACCAGATCTT | 51429 |
| rs752870624 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157880387 | TCTCACTATTCTACC[C/T]TCTCTAATCGTGTAG | 51429 |
| rs752875743 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157792374 | TCGATCTCTCGTCCT[C/T]GTGATCTGCCCGCCT | 51429 |
| rs752882555 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157867354 | GAACAGAACAGGGCT[A/G]TCACCGTTGGTGTTA | 51429 |
| rs752884276 | snp | A/G | 1.8667e-05 | 0.00305502 | intron-variant | SNX9 | GRCh38.p7 | 6:157902081 | GGGAACCAGGGCCGT[A/G]GTAGAAGTATACATT | 51429 |
| rs752896543 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157908995 | GCTTAGGCACATAGC[A/G]GTCCACGGAAGAAAA | 51429 |
| rs752921974 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157814430 | AAAATGTACCTGTCT[A/T]TCAAGAAAGCTCAGA | 51429 |
| rs752959467 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157825158 | GAGGCTGAGGCAGGA[A/G]AATCGCTTGAACCCG | 51429 |
| rs752962000 | snp | A/G | 4.95692e-05 | 0.00497816 | intron-variant | SNX9 | GRCh38.p7 | 6:157921523 | CATTCTTGGTGTGTC[A/G]CTTGCAGGCCGCTTT | 51429 |
| rs752962454 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157927573 | TGAGGAAGCAGTCTC[-/T]TAACCTGCTTTTTCT | 51429 |
| rs752966240 | snp | A/T | 2.67083e-05 | 0.00365424 | intron-variant | SNX9 | GRCh38.p7 | 6:157938782 | ATGAGGTGCTGGTGG[A/T]AGTTTTTTTTTCCCC | 51429 |
| rs753007317 | snp | C/T | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157891928 | ATGGGGAATGCAGCA[C/T]GAGGCAAAGTTGAGA | 51429 |
| rs753019091 | in-del | -/TTTTCTCCTTA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157932960 | AGTGTGTGTTGCCTG[-/TTTTCTCCTTA]ACTCATAACTGTTTC | 51429 |
| rs753033379 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157733696 | AAAGAGAGGGATGCC[A/C]TCCCCAGATCTCCTC | 51429 |
| rs753056466 | snp | A/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890410 | CCCAATGTCAAGCCT[A/G]CATAAATATATTTCT | 51429 |
| rs753065671 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157761488 | TTGTTTTGTGTGTGC[A/G]GTCAAATAAGTCAGA | 51429 |
| rs753080871 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157807879 | ATTCCCAGTGAAATA[C/T]TGAAGTTCCAAACCT | 51429 |
| rs753081993 | snp | C/G | 1.64773e-05 | 0.00287026 | missense | SNX9 | GRCh38.p7 | 6:157901969 | TACTTTAAGGATTCA[C/G]AGTCAGCTGATGCAG | 51429 |
| rs753083562 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157782115 | TCTACTGTTAGTTTC[C/T]CCCATATATCTACCT | 51429 |
| rs753125669 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157755585 | CTCAGTCGGATTATA[C/T]GGTGACAATGTCACT | 51429 |
| rs753140572 | snp | A/G | 1.64942e-05 | 0.00287173 | missense | SNX9 | GRCh38.p7 | 6:157932254 | TTGGCCACAGTGTTC[A/G]GTTCCAGTGGCTATC | 51429 |
| rs753150061 | snp | C/T | | | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822684 | GAAGCCATCGCTCCG[C/T]TCCTTCCCAGCTGTT | 51429 |
| rs753151779 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157813640 | CAATTACAACAAATT[C/T]AGTTTCAAGATCCTA | 51429 |
| rs753155928 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157830048 | TAAGGTTATTTAACT[C/G]CAGTCATCTCCCCCA | 51429 |
| rs753204875 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157772802 | TTGAGCCCAAGTAAG[C/G]AGCCTCAATATGGGA | 51429 |
| rs753210950 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157857284 | GCTAGTAGTGTCTTT[A/G]ATAATCTGATAGGAA | 51429 |
| rs753218705 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157898934 | TCTGGCTCTCTGGTC[A/G]CTTGGCCCACATCCT | 51429 |
| rs753218833 | snp | A/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886886 | TTTTCTTTGTGCTTA[A/G]AGTTATCACCTTTTG | 51429 |
| rs753230576 | snp | C/T | 1.67984e-05 | 0.00289809 | intron-variant | SNX9 | GRCh38.p7 | 6:157932159 | CCATTTCAGTTTGCT[C/T]AGAAGACTAATCGTT | 51429 |
| rs753244252 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157745139 | GAGTCAAGCAGAGCT[A/G]AATTCAAGGCCCAAT | 51429 |
| rs753267959 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157944707 | AAGCGTATCATAACC[A/G]CCTGGGAGTTGCCAA | 51429 |
| rs753279021 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157938299 | AGCCACATGACTTCC[A/G]AAACCTGCTAATGCC | 51429 |
| rs753280072 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157781291 | GGCTCCTTCACCTCC[A/G]TCACCGAGCTGGATC | 51429 |
| rs753284586 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157918072 | TTCCATGTGTGCTTC[A/G]AAAGAATATGTGTCT | 51429 |
| rs753294233 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157898142 | GATGGCTATTTCTTA[C/T]CTCACAATACCACTC | 51429 |
| rs753318762 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157779051 | AGTGAATTAGCAGGA[A/G]AGTCCTGTTTCCAGC | 51429 |
| rs753327396 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157743021 | ACTCATTTAATTTAA[A/G]ATTAACAGTCATTGC | 51429 |
| rs753335636 | in-del | -/GT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157765352 | TATATTTGTTTTTTT[-/GT]TTGTTTGTTTGTTTG | 51429 |
| rs753340494 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157742354 | TGTTTGACTCTGTGT[C/T]CTGAACGCCACTGGG | 51429 |
| rs753379365 | in-del | -/GGTCTTG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157765893 | AAAAATCTTCTAAAA[-/GGTCTTG]GGTCCATGAGCATTG | 51429 |
| rs753384111 | in-del | -/AAT | 1.78594e-05 | 0.0029882 | cds-indel | SNX9 | GRCh38.p7 | 6:157935978 | GGTGAAACAGATCTC[-/AAT]GATGCAATAACAGAA | 51429 |
| rs753385326 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157906328 | AAATATATTTAATGC[C/T]CCACATAACTGATAA | 51429 |
| rs753395080 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157883282 | GTAACCATAACTGTT[A/G]TGTACACTGGGGGAC | 51429 |
| rs753406563 | snp | C/T | 4.95111e-05 | 0.00497525 | intron-variant | SNX9 | GRCh38.p7 | 6:157896821 | TCTTTTTACCCCTCT[C/T]AATAGGTTGGCAGTG | 51429 |
| rs753412212 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157865477 | CGTCCTGCTGGCCTG[A/G]GCGCCCTGCCATGAT | 51429 |
| rs753432113 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157834920 | AACCCTAGGAAATCA[A/G]TACCCGTTAGGTTAC | 51429 |
| rs753433987 | snp | A/C | | | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821522 | TGAAGTCATATATAC[A/C]CATGGTCAAAAACTC | 51429 |
| rs753439443 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157783377 | ATCAAGAAAATGGAA[A/G]CTATGAATGACACTA | 51429 |
| rs753439708 | snp | C/G/T | 4.95752e-05 | 0.00497851 | intron-variant | SNX9 | GRCh38.p7 | 6:157932276 | GTGGCTATCAAGGTG[C/G/T]GTCTTTCTTCATTCA | 51429 |
| rs753452534 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157803424 | AAATTGATTTAAGCA[C/T]GTAGCTCATAAACCT | 51429 |
| rs753507257 | in-del | -/TTA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157924560 | TGGGGGTGGAAAGAT[-/TTA]TTAACCAGTTAGCTC | 51429 |
| rs753509909 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157724360 | GTCTGAACTATGCGA[A/G]GTATGCAAAATGTAC | 51429 |
| rs753516176 | snp | A/T | 1.77808e-05 | 0.00298162 | missense | SNX9 | GRCh38.p7 | 6:157935980 | TGAAACAGATCTCAA[A/T]GATGCAATAACAGAA | 51429 |
| rs753530572 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157753780 | TGCCCCGCTGCCTAG[A/G]CAGAGCCAATTCATC | 51429 |
| rs753541296 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157809392 | TGGACCTAAATGTAA[C/G]AGCTAAAGCCATAAA | 51429 |
| rs753552566 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157798935 | TTCTCACGCTGCTAT[A/C]AAGAATACTACCTGA | 51429 |
| rs753562730 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157719322 | AAAATAGACATTGTC[G/T]CTACCCTTTTCCAAG | 51429 |
| rs753567523 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157924795 | TTTAAAAAGATTGGC[-/A]AAAAGTGTTGGTAAT | 51429 |
| rs753576761 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157828930 | AATGCTGTCAGCCTC[A/G]AGAAGCTGAGACTGT | 51429 |
| rs753598321 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157753632 | AAAATCTTTCCACAA[A/G]CCTCCAGATTTCCCC | 51429 |
| rs753626280 | snp | A/C | 1.64879e-05 | 0.00287118 | intron-variant | SNX9 | GRCh38.p7 | 6:157938751 | ACGCGTTGCAAGGTA[A/C]GATGAAAGGGTCCTT | 51429 |
| rs753639220 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157748496 | AGCACTTTGGGAGGC[C/G]AAGGCGGGTGGGTCA | 51429 |
| rs753647970 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157786342 | GCATGAGCCACCATG[C/G]CTGGCCGATCCTTGC | 51429 |
| rs753654078 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157901627 | GTCATCTCGGTGCCC[A/G]TGTCAAAAATTTAAA | 51429 |
| rs753659634 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157719875 | CCGTCTCTACTAAAA[A/G]ATACAAAATTAGCTA | 51429 |
| rs753666889 | in-del | -/TAATA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157937953 | CAACTTCAGATAACT[-/TAATA]TAATATAAAACTCAG | 51429 |
| rs753680864 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157911965 | CTTGAGTGGTCCCTC[G/T]TGGTGCTGGGGCGGT | 51429 |
| rs753684892 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157874091 | CCAGGAGAAAAGAAT[C/T]CCCCCCAGAGGATGT | 51429 |
| rs753700178 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157855462 | ATAGGCATTACCAAA[G/T]TGCCTCTTCTGTTAG | 51429 |
| rs753707143 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157731617 | TCTGACCTCCTGTAG[A/T]TCACCTGGAATTGCT | 51429 |
| rs753708819 | snp | A/G | 1.66754e-05 | 0.00288746 | intron-variant | SNX9 | GRCh38.p7 | 6:157921664 | CCGAGATGAGAAGGT[A/G]GGACATTGTGTTAAT | 51429 |
| rs753725642 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157759310 | CCAAACCAGGCTGTG[A/G]CATGCTAGAGCTGGC | 51429 |
| rs753744736 | snp | A/G | 1.6517e-05 | 0.00287372 | missense | SNX9 | GRCh38.p7 | 6:157875172 | CTGCCAGCAACAATC[A/G]CCAGGTACGTCTCAC | 51429 |
| rs753767726 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157829982 | GGATGTTAACATTAA[A/C]GTCTGAAATTACTTA | 51429 |
| rs753777599 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157861769 | TATGCCTATGACAAA[A/G]TTAATTTATAAATTA | 51429 |
| rs753796453 | snp | C/T | 9.93345e-05 | 0.0070468 | intron-variant | SNX9 | GRCh38.p7 | 6:157921511 | AAAGTTGTATGTCAT[C/T]CTTGGTGTGTCGCTT | 51429 |
| rs753834010 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157785281 | AAAGCATATTTCTCA[A/G]TTCATTCTATGTGGC | 51429 |
| rs753836845 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157845576 | TGTAATCACAACTGG[C/T]TCATGGTAAGTATAT | 51429 |
| rs753851100 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157912767 | GATTTTTGTTTTTTA[C/T]GGAAATAATATTGAA | 51429 |
| rs753852631 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157788498 | GGTTAACTTCTTTTA[-/C]AACTCAGAAAAATCA | 51429 |
| rs753868787 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157764818 | TGTATGGAATGAATA[A/T]CCACATGTGAGAAGA | 51429 |
| rs753882196 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157807188 | CACAGTTATAGGACA[A/C]GGACTCTATTTGAGT | 51429 |
| rs753922114 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157932356 | CTGCAGACGCTAACT[C/G]CCTCCTCAGTGAAGC | 51429 |
| rs753972964 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157806006 | AAGTAAGTGCCTGTC[A/G]TAGTAATAGGCACTC | 51429 |
| rs753982356 | snp | A/G | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157893109 | TGGAGGACACGGAAT[A/G]TATTGCTAAATAGGA | 51429 |
| rs753982550 | snp | C/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894978 | GTGCTGAAGATGAAG[C/G]GACACATTGGGTTTT | 51429 |
| rs753989395 | snp | C/G | 0.000309607 | 0.0124382 | intron-variant | SNX9 | GRCh38.p7 | 6:157928753 | GGGGTGATGCAGGCT[C/G]AGTTTTATGTCCCTT | 51429 |
| rs753995383 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157716914 | ATCAACACAAAGCAA[A/G]TTCAGTGTCCAGTAC | 51429 |
| rs754017139 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157767479 | AAATTATTTTCATGG[C/T]GACCCTCTAGCAGCC | 51429 |
| rs754029179 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157759144 | TCTCTGGGAGGCCAA[A/G]TAGAATAAGGAGTGA | 51429 |
| rs754047591 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157812420 | AAAATTTTGTAAGAT[-/C]AATTTAGTTACATGT | 51429 |
| rs754059633 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157869960 | TACATACTCTTTCAC[A/G]TGTGCACTCTTACAC | 51429 |
| rs754066227 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157869440 | GCTCAGCCTACTCCT[A/C]CTTCTCTGTATTTCT | 51429 |
| rs754070270 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157757319 | GTGTCTAAGTCACCC[C/T]GCATGGGAGAGGCAG | 51429 |
| rs754105860 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157825263 | AAAAAAGAAAAGACG[A/G]GACTCCGTTTGAAAA | 51429 |
| rs754111256 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157814828 | TAGTCAATCTATTGA[A/C]TATCAGGCCAGTTTT | 51429 |
| rs754117379 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157772690 | TAGTTTGTTATGGCA[G/T]CCCAGGAAACTAGTC | 51429 |
| rs754123135 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157901947 | GGATGGGCCCAAATC[C/T]TCTTCCTACTTTAAG | 51429 |
| rs754125469 | snp | A/G | 1.67559e-05 | 0.00289442 | intron-variant | SNX9 | GRCh38.p7 | 6:157875018 | AAGTGACCGTAATCT[A/G]TGAAAATAATTGCGG | 51429 |
| rs754132611 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157846634 | AGAGACTTGCAGATC[A/G]TCTAGGCTGACCCTG | 51429 |
| rs754147150 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157735170 | CCCAGGTACTGGGAA[A/G]GCTGAGGCATGAGAA | 51429 |
| rs754153361 | snp | A/G | 4.98227e-05 | 0.00499088 | intron-variant | SNX9 | GRCh38.p7 | 6:157942755 | GTCGTAATGGGAGTG[A/G]TATCTCAACGTTGTT | 51429 |
| rs754176798 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157870801 | CACCCGTGCAAGCAC[A/G]CACACCCCTCAGACA | 51429 |
| rs754185871 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157733737 | AGATGGTCCCTGCCT[-/C]CAAAGGGGACTTACA | 51429 |
| rs754217971 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157762067 | GATGGGAGAGGTCAC[A/G]GGTGGGGCCGTGCCT | 51429 |
| rs754220934 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157858686 | TGGGTAATTTATAAA[G/T]AAAAGAGATTTAATG | 51429 |
| rs754286836 | snp | A/G | 4.98625e-05 | 0.00499287 | missense | SNX9 | GRCh38.p7 | 6:157873148 | ACATCAAAGGAGAAC[A/G]AGGGCTGGTTCCCAC | 51429 |
| rs754289489 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157750962 | TTTTTAAAAAATATA[A/G]TAAGTGTTGGAGAGG | 51429 |
| rs754309803 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157802506 | TTAATCTTTATAAAG[C/T]ACTACAGGGCAAAAC | 51429 |
| rs754309978 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157763292 | TTGAGGAAGCTGCTC[C/T]GGGCTTCCAGGCCAG | 51429 |
| rs754321558 | snp | A/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889674 | TGGCTGGAATAGAAA[A/G]TATCTTAAGCCTGTT | 51429 |
| rs754333018 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157847883 | TAACTCTCTTGGTAA[A/G]TGTACCTTTGCATTA | 51429 |
| rs754337006 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157746933 | GTGGGGTCAGAGGGT[A/G]TGAAACTGTTCCACC | 51429 |
| rs754356457 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157851568 | CCTATTCTAGGTATC[C/T]CACATAGTGGAATCA | 51429 |
| rs754381262 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157786785 | AGACTGTGCCTACTG[A/G]GTTTACAGCTCTCTG | 51429 |
| rs754426646 | snp | A/G | | | splice-donor-variant | SNX9 | GRCh38.p7 | 6:157928703 | AGCGCTGCACGGGCC[A/G]TAAGTCCACTCCTCA | 51429 |
| rs754438606 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157764917 | TATAATTACAGATCC[C/T]TGTGCTCTGAGGGTT | 51429 |
| rs754441232 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157914537 | GCTGGAGTGCAGTGG[C/T]ACCATCTCAGCTCAC | 51429 |
| rs754476034 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157751128 | AGAGGTTTCATTGGA[C/T]TTACAGTTCCACATG | 51429 |
| rs754476495 | snp | A/C | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886644 | GTTTCATCTAGAAAG[A/C]AGCACTTTCCTGTAT | 51429 |
| rs754496213 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157721755 | GGACCGAGGTTCTTT[A/C]CCTCCTTCCCGCCCG | 51429 |
| rs754501840 | snp | A/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885625 | GTCGTAAGATGGGCC[A/G]TGGCATGATAGGCCA | 51429 |
| rs754535207 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157843821 | TTGAAGACAATTTCA[A/G]AGCATCGTGAGTACA | 51429 |
| rs754539197 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157937106 | ATATTTAGAAGTTAA[A/T]CTACAACAACTCATT | 51429 |
| rs754539299 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157830267 | GAGAAGGTATGTTGT[C/T]GGTAAATCTCTTATA | 51429 |
| rs754547413 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157775455 | TTTTCTTTCAGAGAA[A/G]GAAACCGGATCTTTC | 51429 |
| rs754556877 | snp | G/T | 3.63346e-05 | 0.00426215 | intron-variant | SNX9 | GRCh38.p7 | 6:157906261 | GATTAAGCTCTTTCT[G/T]ATACCGTACTTTAAA | 51429 |
| rs754579403 | in-del | -/T | 1.76157e-05 | 0.00296775 | frameshift-variant | SNX9 | GRCh38.p7 | 6:157936017 | AGACTTATGAAGAAA[-/T]TTGCCAGTCTCGTGG | 51429 |
| rs754605008 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157866755 | TCTTATTAGATAAGG[A/C]GCAGTGAACATTTTA | 51429 |
| rs754605386 | in-del | -/CACAC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157818084 | ATATATACACAAACA[-/CACAC]ACACACACACACACA | 51429 |
| rs754627261 | snp | C/T | 6.62976e-05 | 0.00575712 | intron-variant | SNX9 | GRCh38.p7 | 6:157867532 | ACATCCTCTTTTCCT[C/T]TCCACTCCTGATAGG | 51429 |
| rs754635252 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157833190 | ATAGTTGCCTATTGC[A/G]TAGTGGCTGCACATA | 51429 |
| rs754645980 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157788297 | TTTCAAGGGAAAAAG[C/G]CTGGAGGTTCTTTTA | 51429 |
| rs754660784 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157863097 | CCATTGACAGCAATA[C/T]CAGAGAGAAGGAGCA | 51429 |
| rs754665495 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157921083 | ATGGAAATACCATGT[C/T]GTTTGTAAGAATGAC | 51429 |
| rs754670143 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157903529 | AAGTTTTCAGTCATG[G/T]TCAGTAGTGATGTGC | 51429 |
| rs754690443 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157720230 | ACATCCCTTAGAGTC[A/G]CAAATAGAAGAACCC | 51429 |
| rs754692839 | snp | A/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888213 | CCTCTGAAAGCAAAA[A/G]GTTCAGAATATTAAC | 51429 |
| rs754694824 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157876085 | GATTTTTTTTTTAAC[C/T]ACATAAAAGGTTTTA | 51429 |
| rs754706265 | snp | A/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893237 | CAGCGTCCACTGGGG[A/T]CATCTGAGAGTCCAT | 51429 |
| rs754711660 | snp | A/G | 3.3083e-05 | 0.00406699 | intron-variant | SNX9 | GRCh38.p7 | 6:157921515 | TTGTATGTCATTCTT[A/G]GTGTGTCGCTTGCAG | 51429 |
| rs754731222 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157942218 | TGTGTTCATGGAGCA[A/G]ACATATATTGAGTGT | 51429 |
| rs754733799 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157774960 | TCCCAGTCTCAGGGA[A/T]GTCCTCAGTGGCTCT | 51429 |
| rs754736673 | in-del | -/TACT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840405 | GACTTTTACAAAAAA[-/TACT]TTCTTTCTTTCTTTT | 51429 |
| rs754744871 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157819197 | TCCTGCTTCTCTTTA[C/T]TCCTATAAAGATTCT | 51429 |
| rs754745331 | snp | C/T | 1.75619e-05 | 0.00296321 | missense | SNX9 | GRCh38.p7 | 6:157935997 | ATGCAATAACAGAAG[C/T]AGGAAAGACTTATGA | 51429 |
| rs754787796 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157716991 | CATCTCCGCACTTGC[A/T]GGGCTGCATTTTACT | 51429 |
| rs754797629 | snp | A/G | 4.94222e-05 | 0.00497078 | missense | SNX9 | GRCh38.p7 | 6:157909963 | ACTGGTTATATGAGC[A/G]TCTCCTGGTTAAGTT | 51429 |
| rs754817279 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157768604 | AGCAAATTGCCCTTG[C/G]CTGGTACTTTTTTTA | 51429 |
| rs754819485 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157806250 | CTTATTCTGCTCCAG[C/T]TGGTAAAGCCATCAT | 51429 |
| rs754838963 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157796923 | ATATACACATAATAC[A/C]TATCTAGAAGGTATT | 51429 |
| rs754840395 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157740529 | CCAATGCAGAGGGGG[A/C]AAATGACTGGGTCCC | 51429 |
| rs754846566 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157752095 | GCTCTGGAGGTTAAG[A/G]CAGGAGAATCGCTGG | 51429 |
| rs754848604 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157878846 | TAATTCCATTCATAT[A/G]CATACACTCTTGCTA | 51429 |
| rs754861270 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157910096 | TATCTTCCTGTAAGT[C/T]AGTGATGGCATTTTC | 51429 |
| rs754866674 | snp | A/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157892382 | TCCGAGGGCCGTGAC[A/G]GAAGCTGCAGGAAAG | 51429 |
| rs754902495 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157900379 | ACAGGTTATCAGATA[C/G]ATGGCTCGCAAATAT | 51429 |
| rs754903606 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157776710 | CCCCAGGTCCCATGG[C/G]CCTCTTAGGATGTGG | 51429 |
| rs754946027 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157852804 | GTCTTAAATTCCTGA[A/G]TTTGTGCGATCTGTC | 51429 |
| rs754948615 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157929846 | CAGCAAAGACAATGT[A/C]AGTATTACTATTCAA | 51429 |
| rs754963621 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157727950 | TAATATTCAATTTTA[G/T]GTTTGATTCATATCT | 51429 |
| rs754995706 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157882000 | ATGAAACAGCCTTCT[A/G]TTATTGGAAGAAGAT | 51429 |
| rs755013864 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157815220 | AGGGCTGTCTGTGGG[-/T]TTTTTTTTTTTAGAC | 51429 |
| rs755025545 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | SNX9, LOC107986663 | GRCh38.p7 | 6:157715037 | GACAGAGTGAGACTC[C/T]GTCTCTTAAAAAAAA | 51429 |
| rs755053814 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157724848 | AACTTTCTTTAAACT[A/G]GATTCTGACCCTTTT | 51429 |
| rs755069189 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157725899 | TTACCTGATTCTTCC[A/C]GAACACCAAACAAGA | 51429 |
| rs755076645 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157940774 | ACTGACAACAGCAGC[A/C]AACCAGATTAGGTCA | 51429 |
| rs755091975 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157861728 | GATAATACCAAACCT[C/T]ATGTGTGTACTATGT | 51429 |
| rs755093445 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157866918 | GAGAAAGAAGATAGT[C/T]TGTTGTTGTTGTTAA | 51429 |
| rs755097370 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157918884 | TATTCCCTTCCCTCA[-/T]TTATGCCATTATTTT | 51429 |
| rs755102849 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157816199 | TGCAAATATTGACAC[G/T]GGAGGTAACGGGTAG | 51429 |
| rs755111753 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157736864 | TTTTAGCATGAAGGG[A/G]TGTTGAATTTTATTG | 51429 |
| rs755129951 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157879240 | GTAACAGCAGAAAAC[C/T]GGAATGTAAATGTCT | 51429 |
| rs755130196 | snp | C/T | | | downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157945266 | CACTGGGTGGAACAA[C/T]GTAACTTGATTCATT | 51429 |
| rs755160528 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157812506 | TTCCTTCTTCCTCTG[A/G]GCATACAACTAGACT | 51429 |
| rs755173100 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157759169 | GAGTGAAATTTACCT[A/G]TTGAATTTGGCAACC | 51429 |
| rs755188006 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157871000 | CAGTGCCAAGATCGA[A/G]GAGGGAGAATGAGGA | 51429 |
| rs755195875 | snp | C/T | 1.65081e-05 | 0.00287293 | missense | SNX9 | GRCh38.p7 | 6:157938640 | TTTCACAGGGAGCAA[C/T]AGAAAAAGTGAAAGA | 51429 |
| rs755224450 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157817156 | AAATAAACATTTGTC[A/G]TTAATAAGCCACCCA | 51429 |
| rs755230124 | in-del | -/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886535 | GTATACACACAAACA[-/T]TACAGATATAAATTG | 51429 |
| rs755244271 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157763584 | AGACCAGGGAGTGTC[C/T]CTTCCAGGTGGAACC | 51429 |
| rs755244326 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157773443 | GAGCCAGGCGACCTC[A/G]GCAGGAGCCAGAACA | 51429 |
| rs755245543 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157735157 | GCACACCTCTAATCC[C/G]AGGTACTGGGAAGGC | 51429 |
| rs755249820 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157736728 | GGGCATCGTTGTCCT[A/G]TGCTGGTTTTCAGAG | 51429 |
| rs755263221 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157865327 | CTGGGCAACAAGAGC[A/G]AAACAGTCTCAGGAA | 51429 |
| rs755298447 | in-del | -/AAC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157821036 | TGCTCTTTTTAAAAC[-/AAC]AACAACAACAAAAAA | 51429 |
| rs755345334 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157908949 | CAGGTGGACGTGATA[A/C]CCGGGGGTTGGAAGT | 51429 |
| rs755345469 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157895582 | AAGAATATTGTGTCC[A/G]TATGTGCTGATGTAC | 51429 |
| rs755360163 | snp | C/G | 3.35796e-05 | 0.0040974 | intron-variant | SNX9 | GRCh38.p7 | 6:157867655 | GAACTGTACATTCGA[C/G]TCTGATTGTCCCATG | 51429 |
| rs755361340 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157829886 | GGATTTCTGTCTACC[A/G]TCTTATAGATTGTAG | 51429 |
| rs755369877 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157731910 | ATGGAGCGCACAGTG[C/T]TGGGGAACATCCTGG | 51429 |
| rs755372616 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157838344 | TTTATTCAACAGTCT[C/G]TCTCTAGAATTTATA | 51429 |
| rs755377918 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157753691 | ATATTCCCTCCTAAG[C/G]CAGTCACTGGGACCA | 51429 |
| rs755381519 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157856965 | TTCCTTCATTTATCA[A/G]CTGAAATGCTTGTAA | 51429 |
| rs755385501 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157910347 | ATGTGAAAAATGACA[C/T]CTGAAAAAATAGAAA | 51429 |
| rs755420654 | in-del | -/AG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157781054 | TATATGTAACAATAT[-/AG]AGAGTGTTTCTTTAA | 51429 |
| rs755425341 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157792256 | AAGCGATTCTCCTGC[C/T]TCCGCCTCCAAGTAG | 51429 |
| rs755438852 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157937174 | TTCATGGTGGTATTA[G/T]TTTGGGCCACGTCAA | 51429 |
| rs755469147 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157925314 | AGATGCCACTACACA[C/T]GTGCCAGAATGGCTA | 51429 |
| rs755472800 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157743618 | GTTTTGAAAAAGTTC[A/G]TTTTGACCATTTTTT | 51429 |
| rs755479023 | snp | G/T | 1.72338e-05 | 0.00293541 | intron-variant | SNX9 | GRCh38.p7 | 6:157901851 | TTTCATTTTTATTTT[G/T]GTCTTTTTTTTTTTT | 51429 |
| rs755485173 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157827669 | TCAAGTTCTGGAAAA[G/T]AAATGAAGAATTTTT | 51429 |
| rs755490451 | in-del | -/TGA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157875513 | GGAGGCTCTTGTTGT[-/TGA]GGAGGTCAGTGTCAG | 51429 |
| rs755509772 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157779366 | TTGGAAGTATTACTA[C/T]GGACCTAAGAGCCTT | 51429 |
| rs755511000 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157783246 | AGTACTTCAAACTAC[A/C]TGCCGCAAAAAATGA | 51429 |
| rs755538038 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157811323 | TCCAGAGATGGCTCT[C/T]CTGGGCTCCTTAAGA | 51429 |
| rs755542608 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157897090 | TGCTGTTCCCACACT[C/T]AGCACAACACAGAAC | 51429 |
| rs755551317 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157855986 | ACGCCTGACCTCAGA[C/T]GATCCACCCGCCTCG | 51429 |
| rs755567794 | snp | C/G | 4.35313e-05 | 0.00466516 | missense | SNX9 | GRCh38.p7 | 6:157928659 | TGACGGCGTGAAGGA[C/G]CTGCTGACGGTGGGG | 51429 |
| rs755570800 | in-del | -/A | 8.81096e-05 | 0.00663679 | intron-variant | SNX9 | GRCh38.p7 | 6:157928736 | GTGCACTGGGCTCGT[-/A]GGGGGTGATGCAGGC | 51429 |
| rs755595935 | snp | A/C | | | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157943951 | GCCTCAGCAGTGTAC[A/C]GAGTCCCCGGCGCTC | 51429 |
| rs755599906 | snp | C/T | 3.30022e-05 | 0.00406202 | missense | SNX9 | GRCh38.p7 | 6:157875160 | CCAGTTCGTCGGCTG[C/T]CAGCAACAATCACCA | 51429 |
| rs755600454 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157780288 | AATAATTATAGAGCA[C/T]ACTCACATGTAATGC | 51429 |
| rs755631653 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157932753 | ATACAGGTAGTTGCA[A/C]CTATTTGGGAGGCTG | 51429 |
| rs755652307 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157802361 | TTCCTAATGAGGTGA[A/C]AATGGGGCAACTTGA | 51429 |
| rs755652335 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157788376 | CATAAATCATTGAGC[A/T]AAGGCATCAACAGTG | 51429 |
| rs755664885 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157918232 | CATTATGATTAGTGG[A/C]CTATCTCTCCTTTTA | 51429 |
| rs755676906 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157804809 | AATCACCCCAGCATC[A/C]AGTTGGTTGAATCCA | 51429 |
| rs755685395 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157728819 | AAGCAGCCTTTCTAG[A/G]CAGGGCACAGTGGCT | 51429 |
| rs755734566 | snp | A/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885774 | AAGTAGTTAGCCTGC[A/G]ATTGGGAACTCCTCT | 51429 |
| rs755734594 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157852971 | TTCTTAGTTTTCTTT[C/T]AGAAAAATTAAATGG | 51429 |
| rs755734819 | in-del | -/CTC | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888629 | AGTCACCACCTTCTT[-/CTC]CTTCTCCTTCTCCTT | 51429 |
| rs755735566 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157722769 | GCACTTTGGGAGGCC[A/G]AGGCGGGTGGATCAC | 51429 |
| rs755736604 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157751338 | CCACTGGGTCCCTCC[C/T]ACAACACGTGGGAAT | 51429 |
| rs755749892 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157865096 | TGTAATCCCACACTT[C/T]GGGAAGCCAAGGCGG | 51429 |
| rs755751758 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157852401 | CTCAGAATTCACAAT[C/T]CTCCTTTCCATTTTT | 51429 |
| rs755753683 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157752257 | GTGGTTGTTTCTCGT[C/T]GGGTGGGACGAGAGA | 51429 |
| rs755768432 | in-del | -/AATA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157862771 | TTTTCATTTTTGCTT[-/AATA]AATACAGGTAGTTCT | 51429 |
| rs755818663 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157865341 | CGAAACAGTCTCAGG[A/G]AAAAAAAAAAAAAAA | 51429 |
| rs755827630 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157933557 | TTGACACTTTTAGAC[A/C]AGAAGCGGGCTTTGA | 51429 |
| rs755834785 | snp | A/G | 9.98885e-05 | 0.00706642 | intron-variant | SNX9 | GRCh38.p7 | 6:157932172 | CTCAGAAGACTAATC[A/G]TTTATTCCTTTTTGT | 51429 |
| rs755844576 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157883204 | ATTTTTAGCAATAAA[A/G]TATTTTTAATTAAGA | 51429 |
| rs755847215 | snp | A/G | 3.33383e-05 | 0.00408265 | intron-variant | SNX9 | GRCh38.p7 | 6:157938615 | TTTATTCATACTGTT[A/G]CATTTTATATTTCAC | 51429 |
| rs755852082 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157854187 | ATTTTAAACTTTACT[A/G]TATTTGTATTCCTGT | 51429 |
| rs755868894 | snp | C/T | 1.64806e-05 | 0.00287054 | intron-variant | SNX9 | GRCh38.p7 | 6:157909831 | GAATCATGTTTGGAT[C/T]ACTGATTGCAGCTTG | 51429 |
| rs755906785 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157855040 | CTCCTCTCCTTTAGC[C/G]ATCTTCTTTCCTCAG | 51429 |
| rs755930720 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157923981 | GTGTGGCGGATCACT[G/T]GAGGTCAAGAGTTCG | 51429 |
| rs755960948 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157759157 | AAGTAGAATAAGGAG[A/T]GAAATTTACCTATTG | 51429 |
| rs755961548 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157794038 | AGGCTAAGCTTTCTC[A/G]TGAAGAAGCTGATAT | 51429 |
| rs755962050 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157795329 | GCTTAGGCAAGAGAA[A/T]GGCTTGAACCCAGGA | 51429 |
| rs755990949 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157882248 | ACATCTGTTTGCAAT[A/G]TGATTTACTGAATAT | 51429 |
| rs756009138 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157872679 | AAGTGTGCAGAAGCC[C/T]TTGAGGCAAGGTTCT | 51429 |
| rs756019772 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157899548 | GAGGCCGAGGCAGGC[A/G]GATCACAAGGTCAGG | 51429 |
| rs756029805 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157768717 | AAGAAAATTTTGAAA[C/T]GCACATATCATCTCA | 51429 |
| rs756032586 | in-del | -/TA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157912683 | CTTAGTAGGTGATGC[-/TA]TATGACATTCCTGTG | 51429 |
| rs756046840 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157860399 | TGACAGAGCAAGATG[C/T]GGTCTCTCAAATACA | 51429 |
| rs756062887 | snp | C/T | 3.29516e-05 | 0.00405891 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157909913 | TATTTTGTAGAACAC[C/T]AATCGATCTGTAAAC | 51429 |
| rs756080385 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157805964 | TTCACACATGCATCA[A/G]TTTTTCCCGGCCACA | 51429 |
| rs756088620 | snp | C/T | 2.13067e-05 | 0.00326388 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157928644 | CACCAAGGCCATGGA[C/T]GACGGCGTGAAGGAG | 51429 |
| rs756090206 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157911648 | CTGAAAAAGGAATTC[C/G]AATCTGATCCCATAG | 51429 |
| rs756128931 | snp | C/T | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157892062 | AAGAGCTTTGCAAAA[C/T]AAGGAGTGGGAAGAG | 51429 |
| rs756139917 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157871222 | TCATCTCTACAAAAA[A/G]TACAAAAATTTAGCC | 51429 |
| rs756150575 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157792415 | AAGTGCTGGGATTAC[A/G]GGCATGAGCCACTGT | 51429 |
| rs756153136 | in-del | -/AA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157819817 | CTGTGGCATGATTCA[-/AA]AAAAAAAAAAAAAAA | 51429 |
| rs756164451 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157758084 | GCTGAGGCAGGAGGA[C/T]CACTTGAGCCCAGGA | 51429 |
| rs756169412 | in-del | -/TT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157783643 | AAATACCTCCTTCTT[-/TT]TTTTTTTTTTTTTTT | 51429 |
| rs756174368 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157755934 | GACCACACAGTGTTC[C/T]TTTGAAACTCCTGGC | 51429 |
| rs756183543 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157870882 | CAGCACTCACCCGTG[C/G]AAGCACGCACACACC | 51429 |
| rs756185283 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157879424 | TTCAGTGCACACACA[C/T]ACACACACACCATAG | 51429 |
| rs756203405 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157789519 | GGATTTGGCCATCCC[G/T]CTGTAGACGGCAAAC | 51429 |
| rs756212538 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157810599 | TCCCTTAACTCTTCG[A/G]TTATTGCATTGTAAC | 51429 |
| rs756233537 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157918661 | TTTTCTGTGTTTGCT[G/T]CTTTTTCCTCCTTTA | 51429 |
| rs756235594 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157930829 | ATTCAGTTTTTAAAG[A/G]CAATGAATTAATTTT | 51429 |
| rs756247022 | snp | C/T | 3.32127e-05 | 0.00407495 | intron-variant | SNX9 | GRCh38.p7 | 6:157927223 | TAGAAATGTGAGAGA[C/T]GCTGCCAGGTTTTCT | 51429 |
| rs756256338 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157837276 | AATCTCACATTACCA[C/T]GGAGGCTGGTTACTA | 51429 |
| rs756263572 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157836891 | CCACCGCGCCCGGCC[A/G]AGAACACACATTTCT | 51429 |
| rs756277018 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157780382 | AGGGGTGACTCTTGG[C/T]GTGGCCTGTGATTTG | 51429 |
| rs756284530 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157764799 | TAAGGCTCTTTCTCA[C/G]TACTGTATGGAATGA | 51429 |
| rs756285842 | snp | C/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890828 | TTCAAGCATAGAAGA[C/G]TTAAACGAATTTCAT | 51429 |
| rs756314513 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157774727 | GCTTTCTGCTCTCTT[A/C]GCTGCTCATCTCCCT | 51429 |
| rs756338155 | snp | A/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157891089 | CAGGCTGGAGTGTAG[A/T]GGTGTGAACTCGGCT | 51429 |
| rs756338435 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157737746 | TTAATTGTGACGTTA[A/G]GGTGTTGATTTTAGA | 51429 |
| rs756381912 | in-del | -/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157940487 | CAGTGGTGCAATCCC[-/G]GCTCACTGCAACCTC | 51429 |
| rs756386558 | snp | C/T | 1.72624e-05 | 0.00293784 | intron-variant | SNX9 | GRCh38.p7 | 6:157867677 | TGTCCCATGTGGACT[C/T]ATTTTTAACAAATCC | 51429 |
| rs756402174 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157766205 | CTGGTAACTCTGGTC[C/T]CCCATTTCAAAGGGA | 51429 |
| rs756417355 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157826196 | AGTTTGACAGTCCTT[C/T]ACTGCTAAAGAAAGT | 51429 |
| rs756424200 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157913957 | CTGCCGTAAACATTT[A/G]CATACAGGTTTTTGT | 51429 |
| rs756424949 | snp | A/T | 1.64776e-05 | 0.00287028 | missense | SNX9 | GRCh38.p7 | 6:157940943 | GTGTCATCCGCCTGT[A/T]CCTGGAGCAGCAAGT | 51429 |
| rs756436820 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157926453 | TTACCTTTTTAGAAA[A/G]CAGATAACCTAAATA | 51429 |
| rs756438033 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157867473 | CATGCTTAGAAAGTG[A/T]ACTGTACACCTTTTG | 51429 |
| rs756448899 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157838483 | GTATGTATACATAGT[G/T]TACAGTGAGATAGCT | 51429 |
| rs756452428 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157857296 | TTTGATAATCTGATA[A/G]GAAAAGATGTTCCAG | 51429 |
| rs756455189 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157898155 | TACCTCACAATACCA[C/T]TCTGGGTCATTGAGT | 51429 |
| rs756480382 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157905822 | GGGAACTAGGGGGGC[A/G]TTTTTTCAGGTCTGC | 51429 |
| rs756481165 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157938349 | CTCCTCAAATGGCAG[C/T]GGCTTCTGAATATTA | 51429 |
| rs756496361 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157761493 | TTGTGTGTGCGGTCA[A/C]ATAAGTCAGAAGTTG | 51429 |
| rs756511264 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157745158 | TCAAGGCCCAATTTT[A/G]CTATTTACTGGCTGT | 51429 |
| rs756514117 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157720443 | ATGGAGCGATTGTAT[C/T]TCACAGGGGTCTACA | 51429 |
| rs756521067 | in-del | -/ATTTG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157860799 | GAAGAGTATGGTACA[-/ATTTG]ATTTATGTATTTTAA | 51429 |
| rs756524793 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157937213 | ATTTTACAAACCAAC[C/T]TAAAAATTACATGAT | 51429 |
| rs756525323 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157846321 | ACATTTGTGCTGCAT[C/T]AAAAGCCAGCTGTAG | 51429 |
| rs756540254 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157823835 | GGCGTCCGGCGTCCC[C/T]GCCGCCCCCACGTCC | 51429 |
| rs756567950 | in-del | -/G | | | upstream-variant-2KB, downstream-variant-500B | SNX9, LOC107986663 | GRCh38.p7 | 6:157714923 | CAGTGTGCACCTGTA[-/G]TTCCACCCACTCAGG | 51429 |
| rs756569773 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157721787 | CCTGCTCTTTAGTGC[G/T]ATGCAAGCGACCAGG | 51429 |
| rs756589213 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157801599 | CTAGGCATGGTGGCG[C/T]GCACCTGTAGTCCCA | 51429 |
| rs756598235 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157832304 | TGTTGCCTATCACCC[A/G]TTGTCATCCACAACT | 51429 |
| rs756599239 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157914730 | CGGTCCACCCACTTC[A/G]GCCTCCCAAAGTGTT | 51429 |
| rs756651126 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157781296 | CTTCACCTCCGTCAC[C/T]GAGCTGGATCTGCTT | 51429 |
| rs756654067 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157927327 | AGACTAGACTTTTAT[G/T]AAATGAGTGGGATTT | 51429 |
| rs756659715 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157802847 | AATACCTGTGAGTGT[-/A]CACAAAACTCGATGA | 51429 |
| rs756665084 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157804619 | GGGAACATCAGTCTT[-/T]CCCTTAAGGTTTTCA | 51429 |
| rs756683023 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157800257 | TAAGCAACCATGTGA[C/T]AGAGTTGCTTTGAGT | 51429 |
| rs756686770 | snp | A/G | 1.66197e-05 | 0.00288263 | intron-variant | SNX9 | GRCh38.p7 | 6:157942746 | CACTGTGAGGTCGTA[A/G]TGGGAGTGATATCTC | 51429 |
| rs756692295 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157862329 | AAGATTGAGGAAGAC[G/T]TTAAATATTATACAA | 51429 |
| rs756706494 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157853096 | ATCTAGTATCATTTT[C/T]GTTCTGGTAAAAGCA | 51429 |
| rs756709141 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157813681 | CTTTGCAATTCTAGA[A/G]TCAGGCAACACTTCA | 51429 |
| rs756711660 | snp | G/T | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894584 | ATTCTTTGAGATTGG[G/T]TGCCATCTATTTCCC | 51429 |
| rs756723982 | in-del | -/TTAAGGAAA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157833495 | TCTTAAGTATGGTAC[-/TTAAGGAAA]TTTTCTTCTTCCAGG | 51429 |
| rs756730048 | snp | A/T | 1.64765e-05 | 0.00287019 | intron-variant | SNX9 | GRCh38.p7 | 6:157909903 | CTCTTTCCCTTATTT[A/T]GTAGAACACTAATCG | 51429 |
| rs756737092 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157771387 | GAGTTTTAGGTTCAA[A/G]CATCAGCTCCCTCTT | 51429 |
| rs756744540 | in-del | -/T | 0.240864 | 0.265316 | intron-variant | SNX9 | GRCh38.p7 | 6:157873072 | ACTGTAATCTTTTTC[-/T]TTTTTTTTTTTTTTT | 51429 |
| rs756861173 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157731667 | TTGGGATGATCCCCT[A/G]AAGTTCAGATCCCTT | 51429 |
| rs756866742 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157778001 | ATTTCCTATTACTGC[A/C]ATAACAAATAACAGC | 51429 |
| rs756889329 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157770633 | TCTACTAAAAAAAAA[-/T]AATAATAATACAAAA | 51429 |
| rs756889478 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157842490 | GTAAGAGTAATTCAC[A/G]TAGAGCTGGCTGTGC | 51429 |
| rs756902128 | in-del | -/GAT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157740590 | ATCAGTTTCCAAAAA[-/GAT]GATAGGTGTCCAGCA | 51429 |
| rs756906497 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157905705 | TGGCCTCTGGAGAGA[A/G]CCTGTTGAAAGGCAA | 51429 |
| rs756909357 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157895216 | TTTGTGCACAGCCTC[A/C]GCGAGCTGCTGAAAC | 51429 |
| rs756909724 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157883326 | ATGACTCACTTTAAC[A/G]TGATGGACTGGAACC | 51429 |
| rs756944021 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157940864 | GGAAAACTGATTGAT[A/G]TTCTGATTTGGGTTG | 51429 |
| rs756956616 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157779078 | CAGCTGCCAGTCATG[A/G]GACAAGGGGTGGAAA | 51429 |
| rs756978687 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157872810 | CTGCAAGCCACTTTT[A/G]TTATCTGCCGCAGAC | 51429 |
| rs756988855 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157750024 | AAGACAACCCATGTC[C/T]ATGGATTGAAAGAGT | 51429 |
| rs756991195 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157814831 | TCAATCTATTGAATA[-/T]CAGGCCAGTTTTATG | 51429 |
| rs756993701 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157922559 | TGTTGAAGTGAACAC[A/G]TAGTAAGTCTTAAAT | 51429 |
| rs757009408 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157773518 | TGAGGGCGATGAGAA[G/T]CCATGGAACGGTTTA | 51429 |
| rs757011376 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157843206 | CAAGGGTTGAAGAAT[C/T]GACGAAAATGAAAAT | 51429 |
| rs757017383 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157835413 | AACCCATTCCCCTTC[-/T]TTTTTTTTTTTTTTT | 51429 |
| rs757033514 | snp | C/T | 1.66524e-05 | 0.00288547 | intron-variant | SNX9 | GRCh38.p7 | 6:157875034 | TGAAAATAATTGCGG[C/T]TCTTTCTCCTATTCA | 51429 |
| rs757046569 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157828954 | AGACTGTTTGTGATC[A/G]CTTTTGTATCTTCAA | 51429 |
| rs757051730 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157925219 | TACTTCATAAAATAA[A/G]GTATCTGAATCAACA | 51429 |
| rs757103794 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157884249 | GTGGTATTTAAGGAT[A/G]TAACATTTTTCTCTA | 51429 |
| rs757111690 | in-del | -/CTT | 1.65083e-05 | 0.00287296 | intron-variant | SNX9 | GRCh38.p7 | 6:157896804 | GTCACAAAAATTCTC[-/CTT]CTTTTTACCCCTCTC | 51429 |
| rs757145346 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157798444 | AGAAATGTAATGCTC[G/T]ACCCTAGGCTGGATC | 51429 |
| rs757152843 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157817340 | CTTCAGCACTCAGCA[C/T]TCAGCAGTGGGTGGG | 51429 |
| rs757159729 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157759676 | AGCCTGGGCAACAGA[A/G]GGAGACCCTGTCTCC | 51429 |
| rs757168327 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157864912 | GCATGCCTGTAATCC[C/T]AGCTACTCGGGAGGC | 51429 |
| rs757171556 | in-del | -/GTG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157939560 | TGAGGGCCTAAAGAT[-/GTG]GTACTGGGGAGAAGA | 51429 |
| rs757172648 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157861834 | TAAAATAGAACAGTT[A/G]TTATAGTATGCCAGC | 51429 |
| rs757180868 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157760084 | CACCATGTTGGCCAG[A/G]ATGGTCTCAATCTCC | 51429 |
| rs757185549 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157917754 | GCTATGTAAATCATT[A/G]TTATACTGTATTGTT | 51429 |
| rs757198405 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157849943 | TCAGTATAAAGATGG[C/T]AGGTGACGTTGTCAG | 51429 |
| rs757202814 | in-del | -/ATATC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157824071 | GCCGGCATGAATAAA[-/ATATC]AAGAGGGAAATGACT | 51429 |
| rs757203679 | snp | C/T | 1.65059e-05 | 0.00287275 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157937493 | TAAAGGTTTTCTTGG[C/T]TGCTTCCCTGACATC | 51429 |
| rs757206487 | in-del | -/TT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157911816 | TGTGGAGATGGAAAC[-/TT]TTGTTTTAAAAGAAG | 51429 |
| rs757236567 | in-del | -/GT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157781813 | ACAGTATCACAAAGT[-/GT]GTATGTGTGTGTGTG | 51429 |
| rs757268841 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157731193 | GAGACAGAGTTTCAC[C/T]GTGTTGGCCAGGCTG | 51429 |
| rs757277859 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157901763 | CCATATTATACTCCT[A/G]TACTATACCCTTTTC | 51429 |
| rs757284084 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157780872 | CATAATGTGTACCTT[C/G]AAGGAAGCACAAACT | 51429 |
| rs757293401 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157782488 | TACCTCTAAGTGGAT[C/T]GTGATAAAGTTGTGT | 51429 |
| rs757294357 | in-del | -/AAAAC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157903999 | GAGTCACTTAAACTT[-/AAAAC]AATTATAAAAAATGT | 51429 |
| rs757297983 | in-del | -/ACTC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157858847 | GATCTCATGAGACTT[-/ACTC]ACTACCACGAGAACA | 51429 |
| rs757307190 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157836016 | TCACAGCAGCAGCCT[C/T]GACCTCCCAGGCACA | 51429 |
| rs757313825 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157746258 | CATTTCTGCATAATT[A/C]TTTTGTGAAGTCTTG | 51429 |
| rs757324227 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157755915 | GGAAAGACAGTGTGG[C/G]TCAGACCACACAGTG | 51429 |
| rs757334941 | snp | C/T | 1.68009e-05 | 0.00289831 | intron-variant | SNX9 | GRCh38.p7 | 6:157927061 | TGGGAATTTTGAAGA[C/T]CAGTTTGACTGTGCT | 51429 |
| rs757340344 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157844450 | GATCGGGGTGGTGCC[-/A]AGCTGATCCATCAAG | 51429 |
| rs757366218 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157771598 | AAGAGAAGAGGAATC[A/G]AGGTGGAAAGGATGG | 51429 |
| rs757366838 | snp | A/G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157754241 | TCCAAGCAAGAAGGA[A/G/T]GTCTGCTTTGGCAAA | 51429 |
| rs757381589 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157881794 | AGGCTGAGAGAGGTG[A/T]GGAAGCTGCAGAAGA | 51429 |
| rs757415720 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157880581 | CCTGTTTCTGTTTCT[C/T]TGAAATGTTACTTCT | 51429 |
| rs757447215 | snp | C/T | 1.64768e-05 | 0.00287021 | missense | SNX9 | GRCh38.p7 | 6:157940936 | TACAACAGTGTCATC[C/T]GCCTGTACCTGGAGC | 51429 |
| rs757452019 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157870147 | CATGTGAGCACACAC[A/G]CCCCTCACTCACCTG | 51429 |
| rs757466461 | snp | G/T | 6.6558e-05 | 0.00576841 | missense | SNX9 | GRCh38.p7 | 6:157896956 | AACACTCCCAACAAC[G/T]GGGACACTGCCTTCG | 51429 |
| rs757476123 | snp | C/G | 1.6504e-05 | 0.00287258 | missense | SNX9 | GRCh38.p7 | 6:157896854 | AATGACCCCTGGTCA[C/G]CCTGGAGTGCCTCCA | 51429 |
| rs757493508 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157772978 | GAGAAAGCAGACGAC[A/G]GGAGCTTCTCCCAAC | 51429 |
| rs757521050 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157826366 | TTAGCTGGGCGTGGT[A/G]GCGGGCGCCTGTAGT | 51429 |
| rs757521053 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157938555 | AATCAGTTATAGAAT[A/G]TATTAGCATTGTTAT | 51429 |
| rs757521226 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157813787 | CAGAGAACAAAACGC[A/G]CACTGGTCCTTTCAA | 51429 |
| rs757557394 | snp | A/G | 3.55448e-05 | 0.00421558 | intron-variant | SNX9 | GRCh38.p7 | 6:157906089 | AAAATTCTTACAAGG[A/G]AAGTCTTAAGACTGA | 51429 |
| rs757558151 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157719596 | TAACTCAATTAGATG[C/T]GAAATGTGCTTAGAA | 51429 |
| rs757568249 | snp | G/T | | | utr-variant-5-prime | SNX9 | GRCh38.p7 | 6:157716146 | TGACAAGGGTCATTG[G/T]GTGTTTTGCTGCTTA | 51429 |
| rs757587297 | snp | A/G | 3.30191e-05 | 0.00406306 | missense | SNX9 | GRCh38.p7 | 6:157932267 | TCAGTTCCAGTGGCT[A/G]TCAAGGTGCGTCTTT | 51429 |
| rs757607330 | snp | A/G | 1.64928e-05 | 0.00287161 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157927182 | ATTTTCCACCATGGA[A/G]CCAGAGGCACCTGAC | 51429 |
| rs757616792 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157846730 | TAATTCATGGTTATG[A/T]TGGTGACCTTGAGTC | 51429 |
| rs757645466 | snp | C/T | 3.29734e-05 | 0.00406025 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157901989 | AGCTGATGCAGGCGG[C/T]GCTCAGCGAGGAAAC | 51429 |
| rs757662716 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157772272 | AGGTAGGACTGTGTC[C/T]CCCAAAAGATATGTT | 51429 |
| rs757691070 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157752319 | ATAGAGAAAGAAAAG[C/T]GGGCCGAGGGGACTG | 51429 |
| rs757693622 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157917213 | TTAAAGATGTTAGGT[C/T]TACTCCTTCATTTCT | 51429 |
| rs757717745 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157814961 | AGGCTTGGAGGCTGG[C/G]TCTGATTGCAAGGCT | 51429 |
| rs757730469 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157722137 | CCTCAAGTCTGATGC[A/C]GATGCTCCCAGGTTA | 51429 |
| rs757731378 | snp | A/T | | | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157944020 | ACTACATCCGAAACT[A/T]CACACAGGGTGTTTC | 51429 |
| rs757739250 | snp | A/T | 3.35723e-05 | 0.00409695 | intron-variant | SNX9 | GRCh38.p7 | 6:157867656 | AACTGTACATTCGAG[A/T]CTGATTGTCCCATGT | 51429 |
| rs757770538 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157865610 | GAGAAATTTCAGACA[C/T]GGAGAAAGGTTGGAA | 51429 |
| rs757770857 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157877928 | CGTATTTTTCTTTAA[C/G]TATATCTTTTTAAAG | 51429 |
| rs757771461 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157905303 | AAGTAGAAGCAATGC[A/G]ACTGGAACTTCGTAG | 51429 |
| rs757777245 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157798635 | TTTAGGGGTGATAGG[A/G]TATCATAGCAGCAAT | 51429 |
| rs757786461 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157735171 | CCAGGTACTGGGAAG[C/G]CTGAGGCATGAGAAT | 51429 |
| rs757787691 | snp | C/T | | | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822221 | AGGTCAAATAGAATG[C/T]ATTTAAGAAGACACA | 51429 |
| rs757814924 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157847912 | TATTTGGCCTCTGGC[A/T]TTGTTTTGACCTGGC | 51429 |
| rs757824508 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157884416 | GGCCTTTTTTGGTAG[C/T]CCATTTAAAAATAAA | 51429 |
| rs757835191 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157833662 | ATGTGCCTTCTCCCT[C/T]AGGAGCTTAGAAGAG | 51429 |
| rs757855499 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157925272 | AATCTCATTAGCAAT[C/T]AATAAATACACATTA | 51429 |
| rs757859866 | in-del | -/G | | | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821855 | CCCAGGAGGGCTGCT[-/G]GGTCCAAGGCTACGG | 51429 |
| rs757874869 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157810244 | GGTTTAATTTATATG[A/G]CATTATATCATAAAA | 51429 |
| rs757875113 | snp | C/T | 1.66485e-05 | 0.00288513 | intron-variant | SNX9 | GRCh38.p7 | 6:157938794 | TGGAAGTTTTTTTTT[C/T]CCCAGCAAAGTTTCC | 51429 |
| rs757889431 | in-del | -/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157846833 | AGGCGGATCACTTGA[-/G]GCCAGGAGTTTGAGA | 51429 |
| rs757900618 | snp | C/G | 1.66626e-05 | 0.00288635 | missense | SNX9 | GRCh38.p7 | 6:157896958 | CACTCCCAACAACTG[C/G]GACACTGCCTTCGGC | 51429 |
| rs757908838 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157720055 | ACTCTGTCTCAAAGT[A/G]AAAAAAAAAAGAGTC | 51429 |
| rs757909927 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157903467 | TAATAAAGTGAATAA[-/T]TCTCTGTCTTGTTAG | 51429 |
| rs757911915 | snp | A/T | 1.65086e-05 | 0.00287298 | missense | SNX9 | GRCh38.p7 | 6:157937450 | CAAAGAAAGATCTCC[A/T]TTTCCTGATGGAATG | 51429 |
| rs757914256 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157895390 | AGTAATTTAAAAAGT[G/T]GCTCTATTCCCTTAA | 51429 |
| rs757920002 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157799484 | CCGGAGAAGGAGGGC[A/G]CTACTGGAATTTAGT | 51429 |
| rs757925773 | snp | A/T | 1.65113e-05 | 0.00287322 | intron-variant | SNX9 | GRCh38.p7 | 6:157909636 | TTTTCCATGTAACAA[A/T]ATTACTTCTTTCTGG | 51429 |
| rs757946744 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157779996 | GTGTAGTTTTCATGA[A/G]TTTCAGAGAATCTTC | 51429 |
| rs757981010 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157842602 | AATTTGGTGGGTAGG[A/G]GCTTGGGAAGTGGGG | 51429 |
| rs757982091 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157719969 | ACCTGGCAGATGGAG[A/G]TTGCAGTAAGCCAAA | 51429 |
| rs757991086 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157753583 | AACAAGGATCTGTGT[C/T]TTTTTTTTCCCTCTA | 51429 |
| rs758001279 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157769646 | CCACAGTAGACACAC[A/C]AAGGCCGGAGAAGGC | 51429 |
| rs758003397 | snp | A/G | 1.75807e-05 | 0.0029648 | missense | SNX9 | GRCh38.p7 | 6:157936011 | GCAGGAAAGACTTAT[A/G]AAGAAATTGCCAGTC | 51429 |
| rs758045577 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157845981 | ACACTTTCAGTGTTA[C/T]TGATTTGCAAGAAGG | 51429 |
| rs758052883 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157743369 | AATATCATTTTACAA[C/G]TAAGAAGCCCATTGG | 51429 |
| rs758059882 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157913588 | AGCTACCACTGCAGT[C/G]CTGCAACCACCACTA | 51429 |
| rs758067905 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157900867 | CCGTAGAAACAGGAC[A/G]TGAAGCTAGACAACC | 51429 |
| rs758069823 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157931033 | CTCCATGTCCTGTGT[A/C]ATTCACAAGGCTAAA | 51429 |
| rs758105839 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157785660 | AAACCTACAGCCTAC[A/G]TCATACTTAATGGTG | 51429 |
| rs758110371 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157740043 | CCACGGCACTTGTAT[A/G]CCTATGTAACAAACC | 51429 |
| rs758120364 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157925483 | CCACTCCTGGATATG[C/T]ACTGAATAGAAATGC | 51429 |
| rs758137486 | snp | A/G | 2.11182e-05 | 0.00324941 | intron-variant | SNX9 | GRCh38.p7 | 6:157873058 | CTCCAGGAAATCTCA[A/G]CTGTAATCTTTTTCT | 51429 |
| rs758144278 | snp | C/T | 8.24967e-05 | 0.00642196 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157896841 | GGTTGGCAGTGGCAA[C/T]GACCCCTGGTCAGCC | 51429 |
| rs758146042 | in-del | -/AC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157723066 | CCCTTGTATGAGGAC[-/AC]ACACACACACACACA | 51429 |
| rs758154027 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157942674 | TGGTGCCAAAAAGAC[C/T]AGTTAAAGAATTGGA | 51429 |
| rs758175318 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157843624 | TCAAAGGTTAACTGT[A/T]CTGATTATCTTATTT | 51429 |
| rs758195548 | snp | C/G | 3.29549e-05 | 0.00405911 | missense | SNX9 | GRCh38.p7 | 6:157909785 | GAATATCAGCTAACA[C/G]CTACTGTAAGTATCC | 51429 |
| rs758197510 | in-del | -/AAATAAAT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157769054 | CAAAAATAAATAAAT[-/AAATAAAT]AAATAAATAAATAAA | 51429 |
| rs758220337 | snp | A/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890974 | CAGAACTCAGACACT[A/G]TTATTTTAAGGGTAC | 51429 |
| rs758222811 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157838702 | TGGTGTTAAATACTT[C/G]AAGGCATGTTTAGTT | 51429 |
| rs758225593 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157817516 | ATAAAGCAAGGATAT[A/G]AGAGTGTGTCAGTGT | 51429 |
| rs758230481 | in-del | -/T | 1.65121e-05 | 0.00287329 | intron-variant | SNX9 | GRCh38.p7 | 6:157896780 | TGAATTGAGTCATGG[-/T]TTCCAAAAGTCACAA | 51429 |
| rs758269395 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157776415 | TGGAAAAAAAATCCT[A/G]GGGGAAGATTCTGTT | 51429 |
| rs758269827 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157722680 | CAAATGATCCTCACT[C/T]AGTGTTTTTATCCTG | 51429 |
| rs758276891 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157859544 | AGATTTGCAGAAATC[A/G]AAAAGTGGAGTGATT | 51429 |
| rs758282459 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157862252 | TATGTTAATAGCATA[A/G]TAATGCTCAGGGTCT | 51429 |
| rs758285655 | in-del | -/GGT | 4.98799e-05 | 0.00499374 | splice-donor-variant | SNX9 | GRCh38.p7 | 6:157867633 | CACAATCACAAATCC[-/GGT]AAGAGAACTGTACAT | 51429 |
| rs758294948 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157750283 | AAAACACTATGGTAT[G/T]GGCATAAACACAGAC | 51429 |
| rs758302622 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157881294 | GAGGCACCACAATGG[C/T]GAGCTTAATTGACAT | 51429 |
| rs758303960 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157786581 | TCATTAAAGATTTTA[C/G]CAAGGTCTCAGGATA | 51429 |
| rs758305897 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157806124 | TCTTTCATCAGACTC[G/T]TAACAAGAAAGGATA | 51429 |
| rs758310699 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157851132 | GCATGGTGGCACATG[C/G]CTGTAATCCCAGCTG | 51429 |
| rs758311218 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157852152 | GGATCATATGGTAAT[G/T]CCGTGTTTAACTTTT | 51429 |
| rs758333094 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157818405 | GCCTTCCCCAACCCA[A/G]TGACTCAAATATTAA | 51429 |
| rs758337050 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157727709 | GGAAGTGTGTTTCAT[G/T]TCTGGCTTTGATGTC | 51429 |
| rs758347659 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157939918 | AGGCATCCGAGGGAG[A/G]CAATGAGGTCCTCTG | 51429 |
| rs758352092 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157940137 | CCCGCTGTCCCACAC[A/G]CTGCCCAGCCTTTCA | 51429 |
| rs758389209 | in-del | -/GAGA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157934314 | ATGATTATAGGGAAG[-/GAGA]GAGAGAGATGGAAGG | 51429 |
| rs758393903 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157805028 | AATAATTTTTCTTTA[C/T]GAAGGACTTGTAAGT | 51429 |
| rs758395518 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157737864 | TGTGTCTTTGTTCTC[A/G]TTGGTTTCAAATAAC | 51429 |
| rs758437382 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157775057 | TCAACACAAACGCCA[C/T]GCAAAGACTTTAGCA | 51429 |
| rs758439333 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157801700 | ACCACTGTACTCCAG[A/C]CTGGGAAACAGAGTG | 51429 |
| rs758488909 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157746355 | ACACAACTTGTTTCC[C/G]CTTTAAAAAAAAAAA | 51429 |
| rs758493244 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157876268 | ACCATCCTGGCCAAC[A/G]TGGTGAAACCCCATC | 51429 |
| rs758501161 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157848101 | CTGGAATTGCTTTGC[C/G]TGTTGATGGCTGTGT | 51429 |
| rs758503033 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157830087 | AATTATTGCCCAGTA[-/T]TTTAGTTATATCTTT | 51429 |
| rs758503932 | snp | A/C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157772854 | GGAGGCCACTAGAGC[A/C/G]TGGAGCTTAGGAAAT | 51429 |
| rs758518107 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157860761 | CTGCACGAGTGAACT[A/G]CAGAGAGAGGGAGAG | 51429 |
| rs758536779 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157796010 | GAAGTGTGACTTGAC[A/G]AATTGGCATTTTAGG | 51429 |
| rs758537343 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157723116 | TTCAGCACCTGAAAA[C/T]ATCCATCTCTCTAGC | 51429 |
| rs758542222 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157928772 | TTTATGTCCCTTATC[A/G]TAGAGGGGAACCTGC | 51429 |
| rs758542617 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157910737 | GCAGGTAGAAAGGGT[A/T]TGTTTTTGTGTCAGG | 51429 |
| rs758548436 | in-del | -/TTTA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157913305 | TCTATCTATATTTTA[-/TTTA]TTTATTTATTTATTT | 51429 |
| rs758582655 | in-del | -/CCG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157897658 | AATTACAGGAGCCCA[-/CCG]CCCACCGCCACACCC | 51429 |
| rs758585282 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157782817 | CCTAAACCCCAGAGG[C/T]GGAGGTTGCAGTGAG | 51429 |
| rs758609126 | snp | C/G/T | 4.95588e-05 | 0.00497768 | intron-variant | SNX9 | GRCh38.p7 | 6:157921524 | ATTCTTGGTGTGTCG[C/G/T]TTGCAGGCCGCTTTG | 51429 |
| rs758623805 | snp | A/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157888103 | GTCATTCACAGCTGC[A/G]ATTGGTAGGACTCAC | 51429 |
| rs758627422 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157786697 | CACAATAAAAAACAT[A/G]AAATACTTTGGGATA | 51429 |
| rs758627481 | in-del | -/CTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840718 | GATTGACACAGTATC[-/CTT]CTCTATATGAGGAAT | 51429 |
| rs758647451 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157717733 | GGATGGGCCTTCAAA[C/G]CATAGCTATAGAAAT | 51429 |
| rs758682334 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157747070 | TGATCTGACAGAAGG[C/G]AGAGCTCAGGCGGTA | 51429 |
| rs758708033 | snp | G/T | 6.64772e-05 | 0.00576491 | intron-variant | SNX9 | GRCh38.p7 | 6:157901865 | TGGTCTTTTTTTTTT[G/T]TTTAACTGATGATCT | 51429 |
| rs758732847 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157851052 | CTTGAGGCCAGGAGT[C/T]CAAGACCAACCTGGC | 51429 |
| rs758750001 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157807937 | TTTACAGTGCCTTCA[C/T]TGTGTGAAAATTTAC | 51429 |
| rs758753700 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157906944 | ATCCTGGACTCAATC[A/G]AGGATGAGGAAACAT | 51429 |
| rs758756548 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157877163 | AAAACTCAGATTTAA[C/G]TCATGTTCTGTTAGG | 51429 |
| rs758757406 | snp | C/T | 1.64757e-05 | 0.00287012 | missense | SNX9 | GRCh38.p7 | 6:157940909 | CACTTTCACAGTAAC[C/T]GGATCTATGATTACA | 51429 |
| rs758768878 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157835228 | ATATTGGCCAGCCCA[C/G]TTTCAAACTCCTGAC | 51429 |
| rs758800098 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157918351 | CTCTTATATCATGAG[G/T]TGTCCCCCATTGTCT | 51429 |
| rs758818249 | snp | C/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889878 | ACATATTAAGATAAC[C/G]TCTACTGAATGCATA | 51429 |
| rs758818903 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157742547 | TGGTTCCCAAACCTG[A/G]CCTGTTGTCAGAATC | 51429 |
| rs758852009 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157784119 | TCAACTATCCAAGTA[C/T]CCATCTTTAAAAAAA | 51429 |
| rs758859742 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157803749 | ATTTTGCTTGTATGT[G/T]AATTTCTTCTGTTTC | 51429 |
| rs758867459 | snp | G/T | 1.9871e-05 | 0.003152 | intron-variant | SNX9 | GRCh38.p7 | 6:157902089 | GGGCCGTGGTAGAAG[G/T]ATACATTAATACAAA | 51429 |
| rs758869452 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157935229 | TATGGAAGTATTTCA[C/G]CTAATAAAGAAGGAA | 51429 |
| rs758871291 | snp | C/T | | | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821805 | CTTTGATGAACATCT[C/T]TGAACACTTGTACAA | 51429 |
| rs758916115 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157724819 | CAGCCATCTTGAAAC[G/T]TGGAGCTTGAATAAA | 51429 |
| rs758921382 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157854713 | AAATTATTGGTTCTC[A/C]GAATGAAAAGTCTAG | 51429 |
| rs758929607 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157939368 | AATAAATTTTGATTG[C/T]GAAGGAACTTGAAAG | 51429 |
| rs758948494 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157797818 | CATCAAAATAAGTAA[-/C]TATAGTAAGGGATGA | 51429 |
| rs758959384 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157820468 | CCAGTCTCTCTCTCT[A/C]TATACAAATATATTC | 51429 |
| rs758975444 | snp | A/T | 1.64806e-05 | 0.00287054 | missense | SNX9 | GRCh38.p7 | 6:157901979 | ATTCAGAGTCAGCTG[A/T]TGCAGGCGGCGCTCA | 51429 |
| rs759010208 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157927330 | CTAGACTTTTATGAA[A/G]TGAGTGGGATTTGTA | 51429 |
| rs759036939 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157847459 | CTAAAGTTTTCCTGA[A/T]GGTGTAGATCTTTGG | 51429 |
| rs759039074 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157870532 | CACCTGTGCAAGCAC[A/G]CACACCCCTCAGACA | 51429 |
| rs759056299 | snp | A/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890306 | TTCTGTGGTCCAGTG[A/G]CTCTGCAGTCAGGTA | 51429 |
| rs759058208 | in-del | -/GAG | | | downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157945098 | AAGTCAGTATTTGGA[-/GAG]GAGAGATGAAGGCGT | 51429 |
| rs759068002 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157870271 | TCTCACATCCCCACG[C/T]TCATGCTCTCACATA | 51429 |
| rs759083195 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157733690 | GCTCAGAAAGAGAGG[A/G]ATGCCCTCCCCAGAT | 51429 |
| rs759083479 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157898868 | ACAGGAGCTGCCTGT[C/T]AGCAGGACCAGGGGT | 51429 |
| rs759094728 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157864678 | CCCGTCCCCTGCCCG[-/C]CATTTCTGTCCTGTC | 51429 |
| rs759112971 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157825663 | TTACATTGTGACAAA[C/T]CATTTCCATTTTAAG | 51429 |
| rs759129784 | snp | C/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887721 | GTCCCTGTTACTCCA[C/T]CTTTGTTGTCTGCTT | 51429 |
| rs759139413 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157938264 | AGAGAGTGCCTGTGT[C/G]CACATGCTGCCCTGT | 51429 |
| rs759173448 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157910468 | AGTGAGCACTGGACA[A/G]AGAAGCCACAGAACT | 51429 |
| rs759177850 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157802175 | CCCAGTGGGATCCTC[A/G]TCTTCCCCTCTGCCC | 51429 |
| rs759185090 | snp | A/C | 1.6477e-05 | 0.00287024 | missense | SNX9 | GRCh38.p7 | 6:157940892 | TTGTAGCTGAGATGA[A/C]TCACTTTCACAGTAA | 51429 |
| rs759204449 | snp | C/T | 3.46711e-05 | 0.00416345 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157896988 | CCACCCCCAGGCCTA[C/T]CAAGGACCAGGTGAG | 51429 |
| rs759217264 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157781979 | TCCATTATCTGACTA[C/T]AAACAGAATATCCTG | 51429 |
| rs759226413 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157747063 | GCGCAACTGATCTGA[C/G]AGAAGGCAGAGCTCA | 51429 |
| rs759226612 | in-del | -/ATGTTCTTTG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157930892 | ATCATTTAAATCTGT[-/ATGTTCTTTG]AAAGCCATTTTTCCT | 51429 |
| rs759241612 | snp | A/C/G | 3.30673e-05 | 0.00406605 | intron-variant | SNX9 | GRCh38.p7 | 6:157937424 | ACAATCAGCTTGTAT[A/C/G]TTGTTATAGCCAAAG | 51429 |
| rs759273129 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157771999 | GCACTGCACCCGGCC[C/T]GGCAGCCAAATTTTA | 51429 |
| rs759294376 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157742195 | GGAACAAAAGAGCAG[A/G]GAAGAGAAGAAATCC | 51429 |
| rs759298350 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157754552 | ACATAAAAGTGCTTT[G/T]TTGAAGGTGGGTCTG | 51429 |
| rs759298612 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157883048 | CATTGTCTTGTTTTA[A/G]GAAGTTGCCACAGCC | 51429 |
| rs759324676 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157928476 | GTATTTAAGGCTAAC[A/T]TAGTGAAAGGGGAGT | 51429 |
| rs759352816 | snp | C/G | | | missense | SNX9 | GRCh38.p7 | 6:157906142 | GATTTCCTGGATTTG[C/G]GAAACCTGGCACGGA | 51429 |
| rs759358721 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157877699 | TTTTGTTTTGAGAGC[A/G]GGAACCTCAGAGAAG | 51429 |
| rs759365844 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157803014 | GCACAGTAATGGATG[G/T]CTGGAGAGAAGGTAG | 51429 |
| rs759400685 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | SNX9, LOC107986663 | GRCh38.p7 | 6:157714363 | CGTGACTTCAATAAA[C/G]AGTTTCACCAACTGC | 51429 |
| rs759415548 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157834508 | TGTGCCACCCCCCCG[C/G]CCAATTTTTTAAATT | 51429 |
| rs759418982 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157853841 | CATTTACTGGGCCAT[A/G]TGTGCCGGTCCCTAT | 51429 |
| rs759478482 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157768005 | AGTAGGGGGATCTAC[C/T]CTTCCTGGTTTGTCC | 51429 |
| rs759481383 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157743871 | AATAAAAAAAAAATA[A/G]CCAGGCTTGGTGACG | 51429 |
| rs759483787 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157786324 | AAAGTGCTAGGATTA[C/T]AGGCATGAGCCACCA | 51429 |
| rs759492885 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157752946 | TGACTTTTAACAAGC[A/T]TGCTGCCTTGAAGCA | 51429 |
| rs759508342 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157899808 | TTTGAGGTATACAGC[A/G]TGATGTTGTAATATA | 51429 |
| rs759518598 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157873992 | TGTCTTTCATGTTGG[A/G]TGACAGAAAGAAGCG | 51429 |
| rs759528060 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157821170 | AAAACCAGGGTTATG[A/G]AATTGTTCTGGTGGG | 51429 |
| rs759537746 | snp | A/G/T | 3.34623e-05 | 0.00409026 | intron-variant | SNX9 | GRCh38.p7 | 6:157921669 | ATGAGAAGGTAGGAC[A/G/T]TTGTGTTAATATGGC | 51429 |
| rs759549906 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157941879 | CCTGTCCTCCCTTAC[A/G]GGACGTGGGCCCTAT | 51429 |
| rs759552430 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157724095 | AGTGGGGAGGGGTTC[C/T]CACAATCCCCTCTGC | 51429 |
| rs759573939 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157799382 | GGATTAAATCAATTA[C/G]TCTCACCCAGTGGGT | 51429 |
| rs759609302 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157774641 | AAAGCTGGGAGGAGC[A/G]CCGGATCACATTTCC | 51429 |
| rs759618341 | snp | A/G | 1.64885e-05 | 0.00287123 | missense | SNX9 | GRCh38.p7 | 6:157932245 | TTGCAGAGTTTGGCC[A/G]CAGTGTTCAGTTCCA | 51429 |
| rs759621659 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157844776 | TTTTTTGTGTTTTTA[A/G]TAGAGACAGCATTTC | 51429 |
| rs759629663 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157829897 | TACCATCTTATAGAT[G/T]GTAGGAGCCCACTCC | 51429 |
| rs759665088 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157750853 | AAATGGCCAACGGGC[A/G]TATGGAAAGATGTTC | 51429 |
| rs759668076 | snp | A/G | 1.65767e-05 | 0.00287891 | missense | SNX9 | GRCh38.p7 | 6:157906196 | TAGCAAAACCCAAAG[A/G]GAAAATTCCCATCAT | 51429 |
| rs759670465 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157842848 | GGAGCCAGAGGCTAC[A/C]TGACCCCGAAATTGT | 51429 |
| rs759706782 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157760745 | TCAGGGCAGACGCCA[C/G]CTGGTGGCCTGGTCA | 51429 |
| rs759730154 | in-del | -/T | 0.237812 | 0.249703 | intron-variant | SNX9 | GRCh38.p7 | 6:157938784 | AGGTGCTGGTGGAAG[-/T]TTTTTTTTTCCCCAG | 51429 |
| rs759738681 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157919210 | GAGGATAGTCGTACC[A/G]ATCTGGCTCCATTGT | 51429 |
| rs759742060 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157942529 | TGGTCTGGAAGCGCC[A/G]CTAGGGCAGAGGTGG | 51429 |
| rs759747914 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157897208 | TGACACTGTCTACCT[A/G]GAGTCAGATCAAGGG | 51429 |
| rs759756104 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157925634 | AGCAATGAAATGAAT[A/G]AACTGTAGTTCTACA | 51429 |
| rs759758644 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157719820 | GGTGGATCACCTGAG[C/G]TCAGGAGTTCGAGAC | 51429 |
| rs759767103 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157760896 | CAAGCAGGTAGGGAG[C/T]GAGAGGGCAGGCTGG | 51429 |
| rs759769118 | in-del | -/TCTC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157813887 | GGGAAATTGCTATTA[-/TCTC]TCTCTCTCTCTCCTG | 51429 |
| rs759769581 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157920485 | TGGTACCACCATGTC[A/G]AACACGTGGGGTGGG | 51429 |
| rs759782630 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157863645 | TCTTTCAAAGACCAC[A/G]TGGAAAATAGATGGC | 51429 |
| rs759792354 | snp | A/G | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157892904 | TTACACAGCGGAAGA[A/G]AGGTAGAGCTGTTAA | 51429 |
| rs759798201 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157756781 | GATCCCCAGAGGCAA[C/G]AGAGTCAAATATGCG | 51429 |
| rs759806112 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157787251 | AAGTCTACCAGTCTT[A/T]GAACTGCAACTACAC | 51429 |
| rs759811865 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157902822 | ACAAACATGTGCCAC[C/T]GCGCCCAGCTAATTT | 51429 |
| rs759812871 | in-del | -/CCAGGATGTGTCGCCG | 1.64846e-05 | 0.0028709 | frameshift-variant | SNX9 | GRCh38.p7 | 6:157921603 | CAGGATGTGTCGCCA[-/CCAGGATGTGTCGCCG]TCCAGTAATCTCAGA | 51429 |
| rs759817457 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157830925 | GATGATTTCATTTGT[G/T]CTTACCTTCTGTTCA | 51429 |
| rs759855450 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157782662 | GGGAGGCCAAGGCGG[A/G]TGGATCATGAGGTCA | 51429 |
| rs759862121 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157772679 | CTGCTTTGTGGTAGT[A/T]TGTTATGGCAGCCCA | 51429 |
| rs759866839 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157880277 | TAGTGCCGGACACAT[A/G]GAAGATATTTCATAA | 51429 |
| rs759870371 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157716602 | GGGAGGGATGCTTTT[A/G]GCATGAGCGATTTTA | 51429 |
| rs759873909 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157862632 | TAAGAATGGGGCCTT[A/G]GCTTTTGCATTCTAA | 51429 |
| rs759876644 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157903978 | ATTTAACTAAACTGT[A/G]TAAATGAGTCACTTA | 51429 |
| rs759885515 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157832498 | CCAAGTCTTGAAATG[A/T]CTGTGTATTAGTCTG | 51429 |
| rs759908098 | snp | G/T | 1.67111e-05 | 0.00289055 | intron-variant | SNX9 | GRCh38.p7 | 6:157875028 | AATCTATGAAAATAA[G/T]TGCGGCTCTTTCTCC | 51429 |
| rs759935917 | snp | C/T | 3.37718e-05 | 0.00410911 | intron-variant | SNX9 | GRCh38.p7 | 6:157932145 | GAAATAGTTTAATCC[C/T]ATTTCAGTTTGCTCA | 51429 |
| rs759943482 | snp | C/T | 1.64811e-05 | 0.00287059 | intron-variant | SNX9 | GRCh38.p7 | 6:157910040 | GGTGAGTGTGTGTAA[C/T]GCTAAACCCAGGATG | 51429 |
| rs759958525 | in-del | -/GA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157836415 | AATAAGCTTCCATCT[-/GA]GAGAGAAATTGAACT | 51429 |
| rs759975425 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157805772 | GTCTACAGCCCCCAT[G/T]GTATACTCTATTATC | 51429 |
| rs759977349 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157718990 | TGCCTGCTGGGTGGC[A/G]GGCCCTTTCTGTGGA | 51429 |
| rs759979053 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157766021 | ACATATTTTCCAGAA[C/G]ATTTTAATAAATAGT | 51429 |
| rs759980007 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157851903 | CTGTTTGTCCTTTTG[C/T]GTCTGGCTTATTTCA | 51429 |
| rs759981162 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157775957 | GGACCATGGTTTGGC[A/G]GTGACATTGTCTGCC | 51429 |
| rs760014307 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157757440 | TGCCCATCAGTTCTT[C/G]TGCCAGGTATACAGA | 51429 |
| rs760053419 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840797 | TAAAAACCTCTATTA[C/T]TTTGCATTCGAGATT | 51429 |
| rs760061100 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157881222 | TTTTCATCATTATTA[C/T]ATCTGTTTTGATGAT | 51429 |
| rs760092132 | snp | A/G | | | missense | SNX9 | GRCh38.p7 | 6:157921651 | AGTTCCTAAATTTCC[A/G]AGATGAGAAGGTAGG | 51429 |
| rs760114890 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157794240 | AGTTCCACTGCACAC[A/G]CTCTCTTGCCTGCCA | 51429 |
| rs760125133 | snp | C/T | | | synonymous-codon | SNX9 | GRCh38.p7 | 6:157909697 | AATGTGGGTTTATCC[C/T]ACCTCTACTTTTGAC | 51429 |
| rs760135322 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157740902 | GACCTTAGTAATGTC[A/G]TTCAATTTCTGTAGG | 51429 |
| rs760135782 | snp | A/G | 1.64882e-05 | 0.00287121 | missense | SNX9 | GRCh38.p7 | 6:157875142 | CAGCCAGCACAGCTC[A/G]GGCCAGTTCGTCGGC | 51429 |
| rs760156428 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157725233 | TTTCGTTCTTATCAC[C/G]GGTTCTGAACAGTTT | 51429 |
| rs760210833 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157753454 | AAGTTGTTTACATTT[C/G]TTCAGTCTACCAGAC | 51429 |
| rs760217762 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157836299 | TGAAAGTGATAGATA[A/G]TGATTCTCTAAAATG | 51429 |
| rs760258692 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157917926 | TCCAACTATCTGGCC[A/G]TTTCCTGAATTTTTT | 51429 |
| rs760272135 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157928593 | GACGGCCGCCTTCAC[C/T]CACAGAGAGCAGAAG | 51429 |
| rs760294541 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157899941 | CGTGCCTGTGGGTGT[A/G]TGTGTGGTAAGAGCA | 51429 |
| rs760321649 | snp | C/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887847 | GATGCTGTCGTCCAC[C/T]ATATAAATGTTTGTA | 51429 |
| rs760326433 | snp | A/G | 1.64844e-05 | 0.00287087 | missense | SNX9 | GRCh38.p7 | 6:157927145 | GGAAGGCCGAGAGAG[A/G]TGAGCTGGCGGGAGT | 51429 |
| rs760354751 | in-del | -/GA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157934316 | GATTATAGGGAAGGA[-/GA]GAGAGAGATGGAAGG | 51429 |
| rs760364065 | snp | A/C | 1.65337e-05 | 0.00287517 | missense | SNX9 | GRCh38.p7 | 6:157896915 | GGGGGGCCCAGCCAG[A/C]GGGGGCTGGAGCCCA | 51429 |
| rs760371288 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157767667 | TCAATGCAAGTTAAA[C/T]GGAACAATTTTGACT | 51429 |
| rs760426431 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157787912 | ATATAAGCAGTGTTC[A/G]ATGAATCTTCATCAA | 51429 |
| rs760427874 | snp | C/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890256 | ATGGGTGTGCGTGTC[C/T]GTCTCCCCCACCCCT | 51429 |
| rs760476831 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157810940 | CCAGGTGTGGTGGTA[C/T]GCACCTGTAGTCCCA | 51429 |
| rs760483452 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157778958 | CCGATGAGCTGGACA[G/T]GTAGGTCAGAACCAC | 51429 |
| rs760487557 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157856598 | CAGAATCCTAATAAA[A/G]TCTGCATATTACTAT | 51429 |
| rs760508861 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157770149 | TGGTACGTGGACTCC[A/C]TCCAAGGCCTCCAGA | 51429 |
| rs760510409 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157791741 | GACAAGCTCTTGCAT[C/T]GCACGGGGGTAATGA | 51429 |
| rs760522939 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157732303 | ATTTACTACCACATC[C/G]CAGCTGGCTTAGGCC | 51429 |
| rs760531279 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157907625 | GTCCCAGGTTTGCAG[C/T]GGTGGTACAGAGCTA | 51429 |
| rs760544711 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157936536 | GACATCTAAATGAAT[A/G]CACTCCAGTATTGAT | 51429 |
| rs760551080 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157742967 | ACCTTAAGTAGACTT[A/T]TATAATAATACTTTG | 51429 |
| rs760564823 | snp | A/G | | | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821347 | TTGTTGAACGGCTGC[A/G]GAGAGAGCTGTACCC | 51429 |
| rs760572004 | in-del | -/T | 3.31647e-05 | 0.00407201 | intron-variant | SNX9 | GRCh38.p7 | 6:157942769 | GATATCTCAACGTTG[-/T]TTTGTTTTGCTTTCT | 51429 |
| rs760584330 | snp | C/T | 6.59131e-05 | 0.0057404 | intron-variant | SNX9 | GRCh38.p7 | 6:157940872 | GATTGATGTTCTGAT[C/T]TGGGTTGTAGCTGAG | 51429 |
| rs760597459 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157934604 | TAAACATGTAGTCAA[C/T]ATCATGTTGGTATTG | 51429 |
| rs760610364 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157841114 | GAACCCTGAGAACTG[G/T]GGCAGAATGCTGTTA | 51429 |
| rs760641241 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157896215 | CCTTAGAATGACTAG[C/G]ATCTCAGGATGTTAG | 51429 |
| rs760663576 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157767202 | GCACTTTAACTCCCC[G/T]GCTCTGAGCGGTTGA | 51429 |
| rs760672906 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157811872 | AGCTGGGTGCCTCTG[A/G]CTGAAGGTCTCTCTT | 51429 |
| rs760674143 | snp | A/G | 1.64825e-05 | 0.00287071 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157938743 | CATGTCTTACGCGTT[A/G]CAAGGTAAGATGAAA | 51429 |
| rs760680341 | snp | A/G | | | synonymous-codon | SNX9 | GRCh38.p7 | 6:157932235 | AGGAAAGGCCTTGCA[A/G]AGTTTGGCCACAGTG | 51429 |
| rs760680348 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157818998 | ACTATGTCCCGTTAC[C/T]GTTTACGGCTCTGTG | 51429 |
| rs760693330 | snp | A/G | 0.000131985 | 0.0081225 | missense | SNX9 | GRCh38.p7 | 6:157942835 | CCGCTTTCCAGTGAT[A/G]TAGGACAGAACGGGC | 51429 |
| rs760693616 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157832912 | TACTCTATCACTTCA[G/T]TTGCTTCAAAAATAC | 51429 |
| rs760700422 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157925056 | GATAAATTAGACTAC[A/T]TTAGAACTTCTTTTT | 51429 |
| rs760701780 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157884050 | AGATTTCCTGAATCC[C/T]TGCCTTGGAGAAGTT | 51429 |
| rs760718810 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157738110 | GAGAAGAAATGTATA[-/T]TCTGATGATTTGGGG | 51429 |
| rs760727191 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157759006 | TGAGGACAGTGGAAG[A/T]AGACCTCAGGTCCTG | 51429 |
| rs760773451 | in-del | -/TTTG | 1.64743e-05 | 0.00287 | frameshift-variant | SNX9 | GRCh38.p7 | 6:157909943 | CACAGGTATAAGCAC[-/TTTG]TTTGACTGGTTATAT | 51429 |
| rs760791794 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157788755 | ATGTTAAATGCTTTT[A/T]ATTAGGTGGCATGAT | 51429 |
| rs760804637 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157876430 | TACTCCAGCCTGGGC[A/G]AGTGAGACTCCTCAA | 51429 |
| rs760809926 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157741038 | GATTCTTAAACGTTG[A/G]TGTTCTAAGAATCAC | 51429 |
| rs760820135 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157904217 | GAGGCAGGCAGATCA[C/T]GAGGTCAGGAATTCG | 51429 |
| rs760841668 | snp | A/G | | | intron-variant, downstream-variant-500B | SNX9, LOC105378078 | GRCh38.p7 | 6:157884882 | TTTTTTTAACCTTAA[A/G]ACTGCAGTGATGAAG | 51429 |
| rs760870620 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157724857 | TAAACTAGATTCTGA[C/T]CCTTTTGATTATTTT | 51429 |
| rs760890071 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157728273 | CAGGTACACCTGGGA[G/T]GGAGGTTCAAGTCAA | 51429 |
| rs760891704 | in-del | -/A | 0.5 | 0 | intron-variant | SNX9 | GRCh38.p7 | 6:157875021 | TGACCGTAATCTATG[-/A]AAATAATTGCGGCTC | 51429 |
| rs760895769 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157916990 | AATTGATACTGTTCT[-/A]ATAAGTGTTTGATAG | 51429 |
| rs760897242 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157795697 | TGTAAAATTAAAGTG[A/G]TAATTTTATAGTAAT | 51429 |
| rs760899547 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157910507 | TTAATGAAGGAAGAA[G/T]CTGCCAGGTTTTCTA | 51429 |
| rs760899924 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157728454 | TCAGAAATCGACTTC[A/G]ACCTTTGCCTTCGCA | 51429 |
| rs760904239 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157903208 | TTTCCCAATATTCCA[A/G]TTCCATGATTCAAGG | 51429 |
| rs760908013 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157915009 | ATTTTTTTTTCACAT[C/T]GGGATATCCAGTGGG | 51429 |
| rs760928146 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157877317 | CATTGAATCTAATCA[G/T]ATCCTTTGAAAGCAA | 51429 |
| rs760939175 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157851450 | TTCTAGAACTTTTTT[-/C]ACCATCCCAAATAGA | 51429 |
| rs760943149 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157839900 | CGTGAATCTCTGCAA[A/C]GCTCAGACCTTTCTG | 51429 |
| rs760959192 | snp | A/G | 1.64743e-05 | 0.00287 | missense | SNX9 | GRCh38.p7 | 6:157901933 | TGGGATGAAGACTGG[A/G]ATGGGCCCAAATCCT | 51429 |
| rs760974913 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157826502 | AGACTCCATCTCAAG[-/A]AAAAAAAAAAAAAAA | 51429 |
| rs760980832 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157923470 | GTAACATCAAAAGTA[G/T]CAAATATCCAGGAAT | 51429 |
| rs760989250 | snp | G/T | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157893023 | GCTGTACCAATGATA[G/T]TCTGTCCCTAGTGTC | 51429 |
| rs761003418 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157746764 | CAGGCTGGGTGACAA[A/G]GCAAGACTTTGTCTC | 51429 |
| rs761005219 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157758573 | GGAAGGGGAGGCTTC[C/T]GGAGTTGGGCAGGAA | 51429 |
| rs761038626 | in-del | -/T/TTCCTTTCTTTCCT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840452 | CTTTCTTTCCTTTCC[-/T/TTCCTTTCTTTCCT]TTCCTTCCTTCCTTC | 51429 |
| rs761067183 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157716553 | CTACGGGGAGACCAG[A/C]AAGAGAGAAGTGGTC | 51429 |
| rs761068828 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157922026 | GTGACTGATTTTCCC[A/G]ATCACGTTGCCCTTA | 51429 |
| rs761073772 | snp | C/T | 1.67716e-05 | 0.00289578 | intron-variant | SNX9 | GRCh38.p7 | 6:157875015 | CTGAAGTGACCGTAA[C/T]CTATGAAAATAATTG | 51429 |
| rs761080274 | snp | G/T | 1.65181e-05 | 0.00287381 | intron-variant | SNX9 | GRCh38.p7 | 6:157937562 | AGAAGACAACAGCAG[G/T]TGAAGGAGGCAGATG | 51429 |
| rs761086171 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157760573 | GTTCTTAGCCTCAGG[-/A]GATGCCAGTGTCACA | 51429 |
| rs761092188 | snp | A/C | 3.2956e-05 | 0.00405918 | intron-variant | SNX9 | GRCh38.p7 | 6:157909881 | GAGTTGGCATTGGTA[A/C]CCTTTTCTCTTTCCC | 51429 |
| rs761114474 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157813896 | CTATTATCTCTCTCT[C/G]TCTCTCCTGATTTTT | 51429 |
| rs761115117 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157771623 | GGATGGTGGAGAATG[A/T]GTCAATGAGATAGTG | 51429 |
| rs761125728 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157738082 | AATTTTAGAATAAGT[G/T]TGATGTAGTGCTGAG | 51429 |
| rs761138749 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157794454 | AACTTATTCAAGTCA[C/T]TAGTTCACAGTAAAG | 51429 |
| rs761163759 | snp | A/G | 1.64754e-05 | 0.00287009 | missense | SNX9 | GRCh38.p7 | 6:157938708 | CAAGACAAACAGAAC[A/G]TGGTGAAGAGAGTCA | 51429 |
| rs761179030 | in-del | -/TGTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157736451 | CATGATTTGGCTCTC[-/TGTT]TGTCTGTTATTGGTG | 51429 |
| rs761182209 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157919058 | TTTCCGGTGCTGCTT[A/G]TTTGTCTCTGCAGAT | 51429 |
| rs761183602 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157768033 | TCCAGGACCATCCCA[A/G]TTTTAAAACAAGAGT | 51429 |
| rs761201443 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157757532 | AACAGTCACAGTTTG[C/G]TATGACATGGCCATG | 51429 |
| rs761209751 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157870661 | TCTCACACAGATGCA[A/G]CACTCACCTGTGCAA | 51429 |
| rs761250802 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157911076 | CGAGATTGCGCCACC[G/T]CACTCCAGCCCAGGC | 51429 |
| rs761250938 | snp | A/G | 1.66457e-05 | 0.00288489 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157873143 | AAGAAACATCAAAGG[A/G]GAACGAGGGCTGGTT | 51429 |
| rs761268123 | snp | A/C | | | upstream-variant-2KB, downstream-variant-500B | SNX9, LOC107986663 | GRCh38.p7 | 6:157715115 | AGTCCCATAGAACCA[A/C]GCCCTTACCCAGGCT | 51429 |
| rs761277812 | in-del | -/ACACTGGCTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157733169 | AGAGCCCAGGCTGCA[-/ACACTGGCTT]ACAAAAATTTGCCTG | 51429 |
| rs761294257 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157744623 | GCATCTCCCCACCCT[C/T]GGAATTGAAAAGGCT | 51429 |
| rs761300745 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157931990 | TTGTCAGTAATAATA[A/G]CATCCACCATTAGTT | 51429 |
| rs761317274 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157782186 | CTTGTCTTGTCACTA[C/G]TCTAAAATTTTATTG | 51429 |
| rs761326268 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157850385 | GGTATTATTCAAAGG[A/C]ATATGTGGGGTTGAG | 51429 |
| rs761347734 | snp | C/T | | | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822484 | ATTTTAGAGACCTCG[C/T]TTCCACTTCAGAGAG | 51429 |
| rs761361477 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157743181 | TATGTTTTTCAGATA[C/T]TTAGTTAAATCCTCA | 51429 |
| rs761365890 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157935673 | CTCGTCATAGGTGTC[A/T]TAATGGTACTGCCTC | 51429 |
| rs761374539 | snp | C/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885437 | ATTCTTCCGTATTTT[C/G]AGCTAAAGTGGTTAG | 51429 |
| rs761394075 | in-del | -/CTAAGGGGGGAGAATCA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157810968 | CAGCTACTCAGGAGG[-/CTAAGGGGGGAGAATCA]CTAAGGTGGGAGAAT | 51429 |
| rs761413262 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157879911 | AATGAGGTTTAAAAG[C/G]TACTTAAAAGTTCTG | 51429 |
| rs761413401 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157851042 | GAGTGAATCACTTGA[A/G]GCCAGGAGTTCAAGA | 51429 |
| rs761428979 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157918121 | GTTTCATTCATGTCA[C/G]TTAGGCTGGGTTGAT | 51429 |
| rs761446683 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157930527 | AGTGAAGCTTCATCT[C/G]TATCTACAGGTGCTC | 51429 |
| rs761466008 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157897032 | GGTCCCACCCTGCCC[A/G]CCCATGGCTGAGTGG | 51429 |
| rs761469657 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157773877 | CGGAGGTGATGAGGT[C/T]GCCTGTGCACGTGTT | 51429 |
| rs761474556 | in-del | -/AG | 1.6476e-05 | 0.00287014 | frameshift-variant | SNX9 | GRCh38.p7 | 6:157940927 | ATCTATGATTACAAC[-/AG]TGTCATCCGCCTGTA | 51429 |
| rs761500979 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157785295 | AATTCATTCTATGTG[A/G]CTATCCTAGCCCTGA | 51429 |
| rs761515392 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157866133 | CCTTGTTTTTACCAC[A/G]GTGATTCTCTCTTGG | 51429 |
| rs761527662 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840423 | TTTCTTTCTTTCTTT[-/T]CTTTCTTTTCTTTCC | 51429 |
| rs761528847 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157725469 | CTGATACAGAACAGC[C/T]GGGCTTCTGGCTAAA | 51429 |
| rs761578956 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157792946 | TTTTCTGTTGTTGTT[G/T]TTGTTTTTGTTTTTG | 51429 |
| rs761585313 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157754890 | AAGGAATAAAGAATG[A/G]CTACTCCATAGACAG | 51429 |
| rs761587523 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157765267 | ATGGATATTCCCGCT[C/T]CCACCACATTGCAGA | 51429 |
| rs761592456 | in-del | -/TTTTTTTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157927721 | TTTAATTTTAAGCTT[-/TTTTTTTT]TTTTTTTTTTTTTTT | 51429 |
| rs761599663 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157867334 | AGAAACCTTCCCTGC[C/T]TCCGGAACAGAACAG | 51429 |
| rs761612018 | in-del | -/A | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889431 | GCAAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 51429 |
| rs761625642 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157845848 | GAAAAGAATTGATAG[C/T]AGATGCTGAATTTGG | 51429 |
| rs761627191 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157925790 | GTAAAACTCTAAACA[A/G]AGTGTCTGAGTCCAT | 51429 |
| rs761655458 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157896500 | ACATAGGAATGGATA[A/C]AGGTTCAGAAAAGTA | 51429 |
| rs761666592 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157926864 | GAAAGAGAACATGGC[C/T]GAATTGGTTCATTCT | 51429 |
| rs761674526 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157732542 | CCCTCGCTTCCTACC[A/G]TTTCCATTTTGTGTG | 51429 |
| rs761686168 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157780839 | GCAACCTCTCAGGAC[A/G]ATGACATTTAGAAGA | 51429 |
| rs761698612 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157824418 | GGGTTTACTTTTGCA[C/G]TTAGTTTTTGTAATG | 51429 |
| rs761704511 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157831218 | GTGTTTTGTGATTTG[A/G]TTTGATTTTTCCTTG | 51429 |
| rs761709739 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157856693 | GTTTTGTCTTTGGGA[C/T]GTATTTGTTGGGATG | 51429 |
| rs761727062 | in-del | -/T | 0.000166041 | 0.00911005 | intron-variant | SNX9 | GRCh38.p7 | 6:157927223 | AGAAATGTGAGAGAC[-/T]GCTGCCAGGTTTTCT | 51429 |
| rs761745066 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157728757 | GTCCTAGGAAAGCAC[A/G]GTTGACACTGGGCTT | 51429 |
| rs761775616 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157770691 | TTTAAGTCCCAGCTA[C/G]TTGGGAGGCTGAGGC | 51429 |
| rs761781037 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157757613 | GGAGGAAGTGACAGA[A/G]GTTGCCCTGCTGATG | 51429 |
| rs761781154 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157861337 | ACATGATAATTAATT[C/G]ACCCGCATCCCCTTG | 51429 |
| rs761815435 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157752676 | ATTCCATTGCCCAGG[G/T]ACGAACATGAGATAG | 51429 |
| rs761819408 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157745621 | CTTGGAAAGTTTGGC[A/G]TTTCCATTCTGCCCA | 51429 |
| rs761834598 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157786353 | CATGCCTGGCCGATC[C/T]TTGCATGTTTAATTC | 51429 |
| rs761835755 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157804596 | TTGGCAGAATTCCCT[C/G]TGCTTAGGGGAACAT | 51429 |
| rs761839451 | snp | A/T | 0.000150418 | 0.00867102 | intron-variant | SNX9 | GRCh38.p7 | 6:157873097 | TTTTTTTGGTGACTT[A/T]TTAGGATGTAGGTGG | 51429 |
| rs761841659 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157874200 | ACCCCTCAGAGAATC[C/T]GATGCAATCTCTAGG | 51429 |
| rs761845093 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157922406 | GGCCCAGAAGCCACA[A/G]CAGATGCTAAATACA | 51429 |
| rs761870556 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157845212 | CTCCTGGGTAGAAGC[G/T]ATTCTCCTGCCTCAG | 51429 |
| rs761876197 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157776855 | CAGGTATGATATTTA[C/T]GGGCTATGTGCCTGA | 51429 |
| rs761888379 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157865940 | GCTAAACTTGAATTT[C/G]CCTTTGAGGACAAAC | 51429 |
| rs761906577 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157807250 | TCAACATTTGAAAAA[C/T]GTGGCTGTTGCAATT | 51429 |
| rs761909102 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157934330 | AGAGAGAGAGATGGA[A/G]GGTAAACTGATTATA | 51429 |
| rs761928771 | snp | A/G | 3.32005e-05 | 0.00407421 | intron-variant | SNX9 | GRCh38.p7 | 6:157941000 | GTCCACGTGCCTTTC[A/G]CATGTGCTTGAGGAG | 51429 |
| rs761937827 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157769355 | CTACTCTGATGCAGG[C/T]GCAGGCACCCCCATC | 51429 |
| rs761950789 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157742037 | CTGGCTCTGCTGGTG[A/G]CCTCAGGAGGATATA | 51429 |
| rs761954332 | in-del | -/AAGCAAAGGGACAT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157858759 | TGGAAGGCAAAGGAG[-/AAGCAAAGGGACAT]CTTACATGGCAGCAG | 51429 |
| rs761966716 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157798859 | CATATATGAAAAATA[G/T]ATAATAAAATGGTTG | 51429 |
| rs762000133 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157938890 | TGCAGGATCCCGGTG[C/G]TGATGAAAATCTGTA | 51429 |
| rs762001614 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840992 | CCATTTCTGATCAGC[A/G]ACTCACTGCATTTCT | 51429 |
| rs762011155 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157795888 | ATCTTTGACGTAGAG[A/G]TGCAAAGCTAGCCAG | 51429 |
| rs762036592 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157784935 | ATACCCATCTTACCC[A/C]ACTCTTAGGAAATAG | 51429 |
| rs762037622 | snp | A/C | 1.67961e-05 | 0.00289789 | intron-variant | SNX9 | GRCh38.p7 | 6:157875009 | GACTCCCTGAAGTGA[A/C]CGTAATCTATGAAAA | 51429 |
| rs762039678 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157923696 | TATTGCGTATCAGAA[C/G]TCATTGTGAAGCTAA | 51429 |
| rs762057601 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157883774 | TTCAGGTTCAGCTCA[A/G]ATACCATGTCTTCTA | 51429 |
| rs762081390 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157872165 | ACCTGCCCCTTAACA[C/T]TGTTAATAATTAATA | 51429 |
| rs762094094 | snp | C/T | 0.00028082 | 0.0118461 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157928611 | CAGAGAGCAGAAGTG[C/T]GAGGCTGTGGGGAAG | 51429 |
| rs762133202 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157743170 | AACTATGATGTTATG[-/T]TTTTCAGATATTTAG | 51429 |
| rs762136961 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157728500 | ATGGGCTTTTGTACT[C/G]CAGTGTATAAATTTA | 51429 |
| rs762138104 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157748965 | CAATATTGAAAAATG[C/G]TTTCAGAGACATTAT | 51429 |
| rs762140162 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157912268 | TGTGTGCTCCACAGT[A/G]TTTAAATCCATGGCT | 51429 |
| rs762142354 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157872969 | ATTTAAGATTTTGAA[A/C]GGTGTTCTCTAGGAA | 51429 |
| rs762154062 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157853774 | TTTTTAGTACATGCA[A/G]ATGTACATGTAATGT | 51429 |
| rs762165776 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157778758 | AATTTTTACCCAGGT[A/C]CAACTGATGCAAAAG | 51429 |
| rs762200650 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157940433 | TTGTTTTGTTTGTTT[A/T]GTTTGAGACAGTCTC | 51429 |
| rs762201928 | in-del | -/GG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157873089 | TTTTTTTTTTTTTTT[-/GG]TGACTTATTAGGATG | 51429 |
| rs762209522 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157797036 | TCTCTGTAAGCCTCA[A/G]TTGCCTCCTTTGTAA | 51429 |
| rs762210442 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157803596 | AGCATACATCAAGGC[A/G]ACTGAAACAGGACCA | 51429 |
| rs762233933 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157860088 | ATGGCCTGCAAACTC[A/G]AAAATATTTACTATC | 51429 |
| rs762253332 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157915485 | ATATATTTTGTTAGA[C/T]TTATGTGTAAGAATT | 51429 |
| rs762280948 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157783941 | AGCCACCGTGCCCAG[C/G]CAATACCTCCTTTTT | 51429 |
| rs762290277 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157828751 | AAGTATTGGGATTAC[A/G]GGTTTGAGACACTAC | 51429 |
| rs762323461 | snp | A/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890381 | CCTTTGAGTGAATGT[A/G]TTTAAATAAGTCTCC | 51429 |
| rs762336623 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157901353 | GTTCCATGTAGTCCC[A/G]CCTGTTATTTTTGAC | 51429 |
| rs762349652 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157916682 | TGTGTACTCATCGAG[C/T]GATTGTATGGCTTTT | 51429 |
| rs762371420 | snp | C/T | 3.53294e-05 | 0.00420279 | intron-variant | SNX9 | GRCh38.p7 | 6:157906245 | TGTTTGCTTTCTTTC[C/T]GATTAAGCTCTTTCT | 51429 |
| rs762388742 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157817002 | ATGCCTTATAAAAGA[C/G]ATCCCACCGCGCTTG | 51429 |
| rs762414577 | in-del | -/CTAA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157790964 | CCTGTGGTCTGGCTC[-/CTAA]CTGTTTCGATCATCA | 51429 |
| rs762463285 | snp | A/C | | | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822580 | GTTAACGGGGCGTCA[A/C]AGAACGAAACCCCCC | 51429 |
| rs762465897 | in-del | -/TAA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157916823 | CTGGATTAAATTTGC[-/TAA]TAATATCTGGTTGAG | 51429 |
| rs762476260 | in-del | -/AA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157753234 | TTCTTTTTAGTGGCA[-/AA]AAAAAAAAAAAAAAA | 51429 |
| rs762476582 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157829481 | ATTATTGATGTGTGT[G/T]TCTATTCTGTATGCT | 51429 |
| rs762511568 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157850842 | GCTGGGCCTGTGCTG[G/T]GGTGCACCAGCTGTC | 51429 |
| rs762511914 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157792673 | AAACTTAATCCTCCT[G/T]CCTAGCTGGATTTTG | 51429 |
| rs762524113 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157868798 | GAACAAAAGCAGATA[C/G]GGAGAATTTGTCTTT | 51429 |
| rs762525509 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157909562 | CAAGAATGACCCTCC[A/G]AAGGACTTCTCATTC | 51429 |
| rs762531234 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157785673 | ACATCATACTTAATG[A/G]TGATTTACTGAACAC | 51429 |
| rs762545143 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157870324 | CACACACCTACTCTC[A/T]CACCTGCGCTCACAC | 51429 |
| rs762565911 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157869623 | CATCCTCTTGCCTGG[A/G]CCATGCACCTTCCTC | 51429 |
| rs762567786 | snp | A/G | 1.69243e-05 | 0.00290893 | intron-variant | SNX9 | GRCh38.p7 | 6:157938582 | TTATATTTTAAACTA[A/G]TGACTAATCATTTCA | 51429 |
| rs762578392 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157925909 | GATCAAGGCACCAGC[A/C]TTTGCTGTCTGGTGA | 51429 |
| rs762578527 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157938139 | AGCCGCTTCCATCTG[A/C]GTCTTTAAATGGATT | 51429 |
| rs762585072 | in-del | -/A | | | downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157945405 | GTTTGATGTTGCCCT[-/A]ACTTACAAGCAAGTA | 51429 |
| rs762601423 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157766735 | GGGTGTGAAATCTGG[C/G]CCATTGATTCTAAGG | 51429 |
| rs762605536 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157898771 | ATTGGGCCAAGAATT[C/G]AATGTCTGTTCTAAA | 51429 |
| rs762615129 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157920304 | TGGAATATGCATGGT[C/T]CAACCTTGGCTATCA | 51429 |
| rs762616838 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157908915 | AATGGAGGCCTACCC[G/T]CTTCAGGCAAGCCTT | 51429 |
| rs762632165 | snp | C/T | 1.64754e-05 | 0.00287009 | missense | SNX9 | GRCh38.p7 | 6:157938691 | CAAGTAAAATCACCC[C/T]ACAAGACAAACAGAA | 51429 |
| rs762654003 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157845300 | TATTTTAGTAGAGAC[A/G]GCGTTTCACCATGTT | 51429 |
| rs762654385 | in-del | -/AC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157818086 | TATACACAAACACAC[-/AC]ACACACACACACACA | 51429 |
| rs762662514 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157824906 | CAGACATTCCAGAAA[C/T]TACCAGTTACACATC | 51429 |
| rs762676360 | snp | C/T | 1.64779e-05 | 0.00287031 | intron-variant | SNX9 | GRCh38.p7 | 6:157909888 | CATTGGTAACCTTTT[C/T]TCTTTCCCTTATTTT | 51429 |
| rs762693509 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157756614 | CTCCAAGATTATCCA[A/G]ATTTCTTGCTCCTTG | 51429 |
| rs762693528 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157788786 | ATAGTGGATGGAGGC[C/T]ATAGGATTGGAATCA | 51429 |
| rs762714123 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157781157 | GTTGAACTTACACCA[C/T]TCATGTTTTTCAAGG | 51429 |
| rs762725745 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157875719 | GGATAACTTGAGAAG[A/G]ATACAAGGAAATTTT | 51429 |
| rs762739337 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157771906 | GTTTCACCACGTTGG[C/T]CAGGCTGGTCTCGAA | 51429 |
| rs762743941 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157856854 | AGCAGGATTGTATTC[C/T]ATCAGAAGGCAAGTA | 51429 |
| rs762746204 | in-del | -/A | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889430 | GCAAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 51429 |
| rs762760862 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157722411 | AGTCTTGCCTGAGCC[A/G]GTGGTCACAGATGAT | 51429 |
| rs762767704 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157834500 | TACAGCTGTGTGCCA[A/C]CCCCCCGGCCAATTT | 51429 |
| rs762774196 | snp | C/G | 3.30158e-05 | 0.00406286 | missense | SNX9 | GRCh38.p7 | 6:157942815 | AAGCTGAGGCAGGCC[C/G]TCAGCCGCTTTCCAG | 51429 |
| rs762780588 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157787981 | GAAACATAAACCAAC[C/T]CTAATAATCAGAGCT | 51429 |
| rs762783530 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157752016 | GCCAACACGGTGAAA[C/G]CTCGTCTCTACTAAA | 51429 |
| rs762790439 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157943681 | TTTGTGGCTTTGGTC[C/G]AACGGGTGAGTGGCT | 51429 |
| rs762800275 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157916594 | TTTATCAAGTTAAGG[A/C]ATTTCTCTTCTATTT | 51429 |
| rs762801812 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157940075 | GAGTTCTGACAGCGT[C/T]GCTGGTGCTCAGGGG | 51429 |
| rs762805702 | snp | C/T | 1.65548e-05 | 0.002877 | missense | SNX9 | GRCh38.p7 | 6:157896939 | GAGCCCAAAGAAACA[C/T]AAACACTCCCAACAA | 51429 |
| rs762806000 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157752697 | CATGAGATAGATGCC[G/T]TCCTCTTATCTCAAC | 51429 |
| rs762815855 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157761073 | CCAAGGAGAAGGAGA[C/G]AGCTGTGGGAGTCAG | 51429 |
| rs762838365 | in-del | -/CATA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157870711 | AGTCTCACCTGCTCT[-/CATA]CATACATGCACTCAC | 51429 |
| rs762840594 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157780258 | TCAACAGGATGTTGT[G/T]GCAATTAGTGGATAA | 51429 |
| rs762868075 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157741253 | CTCAGGAGGCTGAAA[C/T]ACAAGAATCACTGGA | 51429 |
| rs762883825 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157770779 | GTACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC | 51429 |
| rs762890952 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157719077 | CGGCCCACTCTGACC[A/C]CATGCCCAGGTCCTG | 51429 |
| rs762906373 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157761872 | CAGCACATCTGGGGA[G/T]GTTCAATATAGATTT | 51429 |
| rs762917124 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157819104 | AACTAAAACAAACAT[A/G]ATTTTAAAACCATAC | 51429 |
| rs762967477 | snp | C/T | 5.08677e-05 | 0.00504294 | intron-variant | SNX9 | GRCh38.p7 | 6:157906222 | ATCATTGTAAGTTTG[C/T]TTATTTTTGTTTGCT | 51429 |
| rs762977339 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157810287 | ATGACAGAAAGTGGG[A/T]TGTTTGGGACAAGGG | 51429 |
| rs762979361 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157923944 | TGATATTGTTATGTT[C/T]TTAAAACATGTCCCA | 51429 |
| rs762980200 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157825317 | GAGATCTGTCTAGTG[C/G]TGGTCAGTGTGTTTT | 51429 |
| rs762981006 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157789087 | TAGTCCCAGCTACCC[A/G]GGAGGCTGAGGTAGG | 51429 |
| rs763006010 | snp | G/T | 0.000414036 | 0.0143822 | intron-variant | SNX9 | GRCh38.p7 | 6:157901852 | TTCATTTTTATTTTG[G/T]TCTTTTTTTTTTTTT | 51429 |
| rs763010781 | snp | A/G | 9.88435e-05 | 0.00702937 | intron-variant | SNX9 | GRCh38.p7 | 6:157928581 | GCTTATGTGACTGAC[A/G]GCCGCCTTCACCCAC | 51429 |
| rs763019456 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157931867 | GGTAGAGGGGCTATC[A/G]TGATGATCAAGCGCG | 51429 |
| rs763024802 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157855216 | ATCATTCCACACCAG[A/G]AAAGTAAGCAAATCT | 51429 |
| rs763037530 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157744743 | TTCTTTCTTTCTTCA[-/T]TTTTTTTTTTTTTTT | 51429 |
| rs763037544 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157924825 | TTATCGAAGCTGAAC[C/T]TGGGGGGTTTATTAT | 51429 |
| rs763098934 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157924495 | TACTTCCAGAAAAAT[C/T]TCAAAAGTATTGCAA | 51429 |
| rs763103372 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157742422 | AGGGTCATGAAGACT[C/T]GCGGTCAAGTTGAGA | 51429 |
| rs763103407 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157856672 | CCCAACCCTTATCCC[C/T]TACTTGTTTTGTCTT | 51429 |
| rs763145101 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157719767 | GCCGGGCATGGTGGC[C/T]CACGCCTGTAATCCC | 51429 |
| rs763161659 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157877997 | CCTTGACTTTGTATT[A/C]TTAATCTGTGCTGCA | 51429 |
| rs763163489 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157749174 | CTCACATACTGATTC[C/T]GTGAAACCATCAGAT | 51429 |
| rs763165131 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157817914 | TAGCACTTGAGCCCT[A/G]GAGGTCAAGGTTGCA | 51429 |
| rs763180082 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157899915 | TGTGTGCGCGTGTAT[A/G]TGTGCAAGTGCGTGC | 51429 |
| rs763185855 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157739350 | ACATATGAAAAAAAG[C/T]TCATCATCACTGGTC | 51429 |
| rs763188498 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157861612 | TAACAGTGGAGTAAG[C/T]GCAAGGTTGAGCAAA | 51429 |
| rs763191646 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157930560 | CATCACTCACATTAC[C/T]GCCTGAGCTCCGCCT | 51429 |
| rs763197001 | snp | A/G/T | | | synonymous-codon, missense | SNX9 | GRCh38.p7 | 6:157921544 | AGGCCGCTTTGAAGA[A/G/T]GAATTTATCAAAATG | 51429 |
| rs763206443 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157829680 | ATTGAAGTTTTTATC[A/T]TTATGAAGTGAACCT | 51429 |
| rs763219993 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157862525 | AATTGTACTTTTCTG[G/T]TTTAAAGATGAGGAG | 51429 |
| rs763229807 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157940463 | CGCTCTGTCACCCAG[A/G]CTGGAGTACAGTGGT | 51429 |
| rs763231528 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157799281 | GTGGGGACACAGAGC[C/T]AAACCATGTAATTCT | 51429 |
| rs763237804 | snp | C/G | 1.67256e-05 | 0.0028918 | intron-variant | SNX9 | GRCh38.p7 | 6:157867645 | TCCGGTAAGAGAACT[C/G]TACATTCGAGTCTGA | 51429 |
| rs763237817 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157912449 | TTCGGCATGCAGCCA[C/G]GGAGGAGAAAGTCAT | 51429 |
| rs763259534 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157725714 | CAACTGAATGTCAGA[A/G]ATTACGGATAGACGC | 51429 |
| rs763272201 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157764152 | CTGGAGCTAACATAG[G/T]CTTCCGTGGTATTTC | 51429 |
| rs763301678 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157758976 | TCTGGGAAGCAGCGG[C/T]ATTCACGTTCCCAGT | 51429 |
| rs763320962 | in-del | -/TAAAC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157936905 | TTTTTCAGATGACTT[-/TAAAC]TATGTGTATGGATGC | 51429 |
| rs763327221 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157755649 | AGCAATGGCTTGAAA[A/G]GAGTTGTTTTGCATC | 51429 |
| rs763353339 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157756881 | GGCTGTGCCAACCTG[A/C]GGCCGAGGGCCAGAT | 51429 |
| rs763356842 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157786161 | GATCCTCCTGCCTCA[A/G]CCTCCCGAGTAGCTG | 51429 |
| rs763357802 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157791962 | TTAATTAAGGTGATC[C/T]GGAAACACAAGAAAA | 51429 |
| rs763401266 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157773407 | AGAAGTCTGCAGTGG[A/G]GGTGGAGGTAGGTAG | 51429 |
| rs763403063 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157879172 | AGTTCCTCCTGCAGA[A/T]CTGCTCGCAGAACGC | 51429 |
| rs763406909 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157780232 | GAGGGTGGTAAAAAC[-/A]TTTACTAACCTCAAC | 51429 |
| rs763409660 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157838070 | CTGTTGCCCAGGCTG[G/T]AGTACAGTAGCAGCT | 51429 |
| rs763417350 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157850617 | CTTTCTGAAGTTGGG[A/G]TAAAGGTCATGGGCC | 51429 |
| rs763431978 | snp | A/C | 2.17101e-05 | 0.00329463 | intron-variant | SNX9 | GRCh38.p7 | 6:157935938 | ATGCATAACTTATAA[A/C]CACTGATAAAATTGA | 51429 |
| rs763434387 | in-del | -/TT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157744745 | TCTTTCTTTCTTCAT[-/TT]TTTTTTTTTTTTTTT | 51429 |
| rs763437188 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157915074 | TCCATTTATTAGAAA[C/G]ATGTTTGTAAGAGAA | 51429 |
| rs763464858 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157800482 | CTCTGCCAAAAAAAA[A/T]AATAATAATAAGATA | 51429 |
| rs763469374 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157835292 | TGCTGGGATTACAGG[C/T]GTGAGTCACCATGCC | 51429 |
| rs763476138 | snp | A/C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157851692 | CCTCCAGGGTTCAAG[A/C/T]GATTTTCCTGCCTCA | 51429 |
| rs763476359 | in-del | -/TTACT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157911752 | ATTCTCCTTAAAACA[-/TTACT]TTATATTTTACTTTG | 51429 |
| rs763477830 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157776397 | ACGTTCTCTCTCCCA[C/T]TATGGAAAAAAAATC | 51429 |
| rs763493058 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157834769 | CTCTGGTGATGTGAC[A/G]TTCAACCTGGAGGTC | 51429 |
| rs763517490 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157917135 | GTCTTTAAGGGAGTC[A/G]ATTTATTTCATAGAA | 51429 |
| rs763522184 | snp | C/G | 1.64947e-05 | 0.00287177 | missense | SNX9 | GRCh38.p7 | 6:157932255 | TGGCCACAGTGTTCA[C/G]TTCCAGTGGCTATCA | 51429 |
| rs763563348 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157919178 | TCATTATTTATCTGG[A/G]TATGTCTTTATTTTT | 51429 |
| rs763627897 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157778999 | CTTCCCTGTCACAAT[C/G]CCTGTCTAGGAGTTA | 51429 |
| rs763639299 | in-del | -/TTTGT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157765664 | CCCGCCTGAAATGTA[-/TTTGT]TTTGTTTTATCATTT | 51429 |
| rs763651618 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157938586 | ATTTTAAACTAATGA[C/G]TAATCATTTCAGCTT | 51429 |
| rs763652624 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157905383 | TTTACTAAAAGAAAA[A/T]TTCTAAAACCCAAAT | 51429 |
| rs763664359 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157847840 | CAGCAGCAGGGAAGC[C/T]CTGTTGAAAATAAGG | 51429 |
| rs763674141 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157754664 | GTGCCTCTGAGTTTC[A/G]AGAGCAAAATTTCTG | 51429 |
| rs763705524 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157907643 | TGGTACAGAGCTAAG[A/G]GTTCCAGCCTTTCAT | 51429 |
| rs763720591 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157753727 | ATTGCCTGGGGTCAT[C/T]AAGATTCTGCTTCTG | 51429 |
| rs763748625 | snp | C/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889603 | TGTTGTTGACCTTTA[C/G]AGTAAAAATATTTCT | 51429 |
| rs763753936 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157722795 | ATCACCTGAGGTCAG[A/G]AATTCAAGACCAGCC | 51429 |
| rs763755873 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157934776 | TTGGAAACAGTGTGA[A/C]CTCATTACATGATTT | 51429 |
| rs763763493 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157855453 | GTAATCCTGATAGGC[A/G]TTACCAAATTGCCTC | 51429 |
| rs763798735 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157848570 | TTAAAAGAAACTGTA[C/T]TTTCTGTACTTTGAA | 51429 |
| rs763802380 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157935660 | GCCGAATGACAGTCT[C/T]GTCATAGGTGTCATA | 51429 |
| rs763812920 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157763269 | GGGAAAAGGGGAGGG[C/T]GGCGGGGTTGAGGAA | 51429 |
| rs763819523 | in-del | -/C | 1.65081e-05 | 0.00287293 | intron-variant | SNX9 | GRCh38.p7 | 6:157896793 | GGTTTCCAAAAGTCA[-/C]AAAAATTCTCCTTCT | 51429 |
| rs763834460 | in-del | -/AAAAAAAAAAAG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157770805 | GACTCCTTCTCAAAA[-/AAAAAAAAAAAG]ATTTATTATTTTATT | 51429 |
| rs763841048 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157836352 | TCAAACTCCCCTCTT[C/T]TCTGATTCATTAGGA | 51429 |
| rs763848881 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157944688 | GTCAGTGTTGCGGTC[C/T]GGGAAGCGTATCATA | 51429 |
| rs763873000 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157719301 | CGGAGAGGCTCCAGA[A/C]GCAAGAAAATAGACA | 51429 |
| rs763882389 | snp | C/T | 4.94311e-05 | 0.00497123 | intron-variant | SNX9 | GRCh38.p7 | 6:157909890 | TTGGTAACCTTTTCT[C/T]TTTCCCTTATTTTGT | 51429 |
| rs763896938 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157785176 | CTTGAACCTGGGAGG[C/T]GGAGGTTTCAGTGAG | 51429 |
| rs763902686 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157763943 | TCTACGGCAGTGGAA[A/G]AGAGCAAAGCAGGTG | 51429 |
| rs763904083 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157759351 | CCAGGAGCACTCATG[G/T]TTAAATTTTCAGGAA | 51429 |
| rs763918172 | in-del | -/TTGC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157866487 | GCTGAGGTGGGAGGA[-/TTGC]TTGAGCCTGGTAGGT | 51429 |
| rs763927487 | in-del | -/AAGT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157862272 | GCTCAGGGTCTGTGA[-/AAGT]AAGTTCTGTTTCTTC | 51429 |
| rs763931730 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157872734 | GATTCTGTTGACCAG[C/T]GAGGTGGCAGAGGGC | 51429 |
| rs763932830 | snp | A/C | 0.000348817 | 0.0132018 | missense | SNX9 | GRCh38.p7 | 6:157896952 | CACAAACACTCCCAA[A/C]AACTGGGACACTGCC | 51429 |
| rs763933841 | in-del | -/TT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157783642 | CTAAATACCTCCTTC[-/TT]TTTTTTTTTTTTTTT | 51429 |
| rs763956941 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157829911 | TTGTAGGAGCCCACT[C/G]CCAACTTTGTGGAAG | 51429 |
| rs764001656 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157779743 | GAAGTACCTGATGTA[A/G]CAGATATTTGATTAA | 51429 |
| rs764004199 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157854233 | GAGCATGCAGTTTTA[C/T]AATTGGGAAAAGCAA | 51429 |
| rs764007549 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157770497 | AATACTTTTTAAAAA[C/T]GATTTATTGGCCGGG | 51429 |
| rs764013474 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157860882 | ACTCAGATTTAAGTT[A/T]ACACTAAGTATTTCT | 51429 |
| rs764038316 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157843143 | ATGAAGCCTTCTAAG[A/C]CTTTCTGTACAGCTT | 51429 |
| rs764048854 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157725719 | GAATGTCAGAGATTA[C/T]GGATAGACGCAGATA | 51429 |
| rs764048886 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157749111 | CAGTGAATTTTATAT[A/G]GTCAATTACCTTTGG | 51429 |
| rs764051381 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157742987 | ATAATACTTTGAAAT[A/G]TTTTTGTTGGTCTCA | 51429 |
| rs764078665 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157799491 | AGGAGGGCACTACTG[C/G]AATTTAGTAGGTGGG | 51429 |
| rs764081753 | snp | A/G | | | intron-variant, downstream-variant-500B | SNX9, LOC105378078 | GRCh38.p7 | 6:157885052 | TATTTTAGGACTTTG[A/G]GCTATCTGAGTAAGT | 51429 |
| rs764113090 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157774595 | TCTCTGCACACCTGC[C/T]GGGGTCTCCTTCCTC | 51429 |
| rs764115188 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157802801 | CAGACTCCGGATCTT[A/G]CTTGGTGGGCCCCCC | 51429 |
| rs764158898 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157759240 | TGAGTCATGCAGGCT[A/G]CGGGCAGGGGACCAT | 51429 |
| rs764163983 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157798151 | CTAGAAGACAACACT[C/G]TAATCAAGTGATCAA | 51429 |
| rs764164773 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157767335 | GTGACAGTGAGGCCT[A/G]GACGCCTGTCCTCAG | 51429 |
| rs764168826 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157721923 | AAATCCTCCAAGACC[C/T]GTCTTCCAAGTTCAA | 51429 |
| rs764169928 | snp | A/T | 1.69844e-05 | 0.00291409 | intron-variant | SNX9 | GRCh38.p7 | 6:157906226 | TTGTAAGTTTGTTTA[A/T]TTTTGTTTGCTTTCT | 51429 |
| rs764172044 | snp | C/G | 3.32132e-05 | 0.00407499 | intron-variant | SNX9 | GRCh38.p7 | 6:157932300 | TCATTCATCCAGTGG[C/G]CCTTTAGAGCCTTAT | 51429 |
| rs764176314 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157797902 | CTACAATAAATAAGC[A/G]TGGGGAAAAGAAAGC | 51429 |
| rs764176349 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157811893 | GGTCTCTCTTGAGAT[C/T]GCAGTTAGGTGTCAC | 51429 |
| rs764177712 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157794487 | AGGGCTAAAGCCAAG[C/T]CTTCTTACTCCCTAA | 51429 |
| rs764184718 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157925057 | ATAAATTAGACTACA[C/T]TAGAACTTCTTTTTT | 51429 |
| rs764205771 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157852015 | TTTGTATTTTGTTTA[C/T]TCATCCGTTGATGGA | 51429 |
| rs764208165 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157878252 | CTTTATCAGCCAAAA[C/T]GCAGTTCAGCTTGGC | 51429 |
| rs764212506 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157819377 | ATACGTTTATTAGGA[C/T]TGGAATGGCACCAGC | 51429 |
| rs764233797 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157940911 | CTTTCACAGTAACCG[A/G]ATCTATGATTACAAC | 51429 |
| rs764244533 | snp | C/T | 1.67478e-05 | 0.00289372 | intron-variant | SNX9 | GRCh38.p7 | 6:157867505 | GTTTTTACTACTCTG[C/T]TTGTGTTTGTAACAT | 51429 |
| rs764248973 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157852737 | GCAGACCACCATGCC[C/T]GGCTAATTTTTGTAT | 51429 |
| rs764256923 | snp | A/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157892130 | GAGGGAAAGGTGGAA[A/G]GAAAGGACAGAGAGG | 51429 |
| rs764280409 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157922160 | TGGCCTCTCTCTCTG[C/T]CTGCCCCTGTGGCCT | 51429 |
| rs764288242 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157795937 | ACTTCTTATCTTCCT[C/G]TAAGTAAAAAATTTT | 51429 |
| rs764290370 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157857845 | AATATGGGGAGACTC[-/T]TTGAATCCATTTGTA | 51429 |
| rs764297989 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157734354 | TTAAATTGTTTGCTC[C/T]ATTCTAGAGAAGGGA | 51429 |
| rs764309203 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157856814 | GAATAGATTCACATT[C/G]TTTTTTTTTCAAGTA | 51429 |
| rs764341847 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157825249 | CGAGACTCCGTTTGA[A/G]AAAAGAAAAGACGAG | 51429 |
| rs764359116 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157776343 | GTCACAAGAACTCCC[A/G]CTTGTATCACCCCAG | 51429 |
| rs764364309 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157933208 | CTGAAGCAGAAGGAT[C/T]GCTTGAGCCCAGGAG | 51429 |
| rs764368009 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157920620 | CAGGTGGCCATTCGC[A/C]TTTTGTTGATTTCTA | 51429 |
| rs764374898 | snp | A/G | 6.62328e-05 | 0.00575431 | intron-variant | SNX9 | GRCh38.p7 | 6:157940991 | TGAGTGGGCGTCCAC[A/G]TGCCTTTCGCATGTG | 51429 |
| rs764414738 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157869926 | CACCCTCATACACCT[C/G]TCATGCTCTCATACA | 51429 |
| rs764415086 | snp | C/T | 1.64958e-05 | 0.00287187 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157932256 | GGCCACAGTGTTCAG[C/T]TCCAGTGGCTATCAA | 51429 |
| rs764465441 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157899168 | ACACGGGGATTATTG[A/T]CAGAATAGTAGCTAC | 51429 |
| rs764479725 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157870723 | TCTCATACATACATG[C/G]ACTCACCTGTGCAAG | 51429 |
| rs764490282 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157915102 | GAAAAAAAATCAGTT[G/T]ATTGTATTTGTTGGT | 51429 |
| rs764498638 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157782278 | GAGTTCTCCTGTGCG[C/T]ATGCACACTGACCTG | 51429 |
| rs764538206 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157826229 | ATCAGGGTCGGGCGC[C/T]GTCTCACGCCTGTAA | 51429 |
| rs764540092 | snp | A/G | 2.01489e-05 | 0.00317396 | intron-variant | SNX9 | GRCh38.p7 | 6:157902092 | CCGTGGTAGAAGTAT[A/G]CATTAATACAAAGTA | 51429 |
| rs764552277 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157757547 | GTATGACATGGCCAT[A/G]ACAGAGAAGAGTCAC | 51429 |
| rs764552332 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157746115 | ATTGATCAATGGCAT[C/T]CTGCAGATAGAACTC | 51429 |
| rs764594525 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157895247 | TGGCTTTAAGGCCTG[C/T]AGTTGCTTGTCAGAA | 51429 |
| rs764600964 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157860035 | GTTTATATATTGTCT[A/G]TGGTGGCTTTTGCAC | 51429 |
| rs764626446 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157816437 | CAAAAGCTTTAATGA[-/T]TTTTAAAAAGCAGAA | 51429 |
| rs764641827 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157746900 | TTTGTGGAAGGCTGT[G/T]TTTCCACAGGGTGGG | 51429 |
| rs764660183 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157791772 | TTGTTTTTCTCTTAC[A/G]CCTTTCTCAGCTTGG | 51429 |
| rs764671645 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157779475 | TTAATGTAAATGTCA[-/T]TTTTAAAAGACAAAT | 51429 |
| rs764688124 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157907785 | CCCAGAGAAAGCAGA[A/G]ACTAACTCTTTGCTC | 51429 |
| rs764697487 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157814777 | CAGAGTCAGTAACCA[C/T]GGTACAAAAATATTC | 51429 |
| rs764704300 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157879137 | TTTACAATGCATATC[C/T]CTAAGGCCCAGCGGT | 51429 |
| rs764724009 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157783464 | TAATCATTCTTAGCA[A/C]GTGCACATAAAACAT | 51429 |
| rs764730675 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157717628 | GCAGCTCCTAACACC[A/G]AGGTCTTACGCACAG | 51429 |
| rs764742144 | in-del | -/TAAA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157817878 | GACTCTGACTCTAAA[-/TAAA]TAAATAAATAAATAA | 51429 |
| rs764753788 | snp | A/G | 1.65302e-05 | 0.00287486 | missense | SNX9 | GRCh38.p7 | 6:157896918 | GGGCCCAGCCAGAGG[A/G]GGCTGGAGCCCAAAG | 51429 |
| rs764773071 | in-del | -/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157914476 | TCTTTTTCTTTTTTT[-/G]TTTTTTTTTTTTTTT | 51429 |
| rs764808310 | snp | A/G | 1.75542e-05 | 0.00296256 | missense | SNX9 | GRCh38.p7 | 6:157936000 | CAATAACAGAAGCAG[A/G]AAAGACTTATGAAGA | 51429 |
| rs764809680 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157725701 | AGCAGAAAGGCATCA[A/G]CTGAATGTCAGAGAT | 51429 |
| rs764825072 | in-del | -/AAATAAATAAAT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157769050 | GTTCCAAAAATAAAT[-/AAATAAATAAAT]AAATAAATAAATAAA | 51429 |
| rs764835420 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157807763 | TAAACTAAGACTCTG[C/G]AGAAGCTATCCTTTC | 51429 |
| rs764840679 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157744744 | TTCTTTCTTTCTTCA[C/T]TTTTTTTTTTTTTTT | 51429 |
| rs764875357 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157919078 | TCTCTGCAGATTCAA[A/G]TCACCATCTTTAGTA | 51429 |
| rs764878910 | snp | A/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890399 | TAAATAAGTCTCCCA[A/G]TGTCAAGCCTGCATA | 51429 |
| rs764892955 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157811932 | GCACTTATGTCAAGG[C/T]TCAACTAGGGCTTGA | 51429 |
| rs764925198 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157721038 | ATAGTCCCAGCACTT[C/T]AGGAGGCTGAGGCCA | 51429 |
| rs764939938 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157896650 | ATTGATGCTACCTTT[A/T]GTGCTTTCCTACATG | 51429 |
| rs764943486 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157784953 | TCTTAGGAAATAGAA[A/G]AGAAAAGCAAAGGCC | 51429 |
| rs764943550 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157925840 | TACCTGAGACTGGAT[A/G]ATTTATATACAACAG | 51429 |
| rs764947341 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157754893 | GAATAAAGAATGGCT[A/G]CTCCATAGACAGAGC | 51429 |
| rs764951700 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157750978 | TAAGTGTTGGAGAGG[A/T]TGTGAAGAAATTGGA | 51429 |
| rs764971347 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157915641 | AAAAAAAAAAAAAAA[-/T]TATATATATATATAT | 51429 |
| rs764974928 | in-del | -/AACTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157843320 | TTTCGACTCCCCCAA[-/AACTT]AACTACTAATAGCCT | 51429 |
| rs764976141 | snp | C/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886351 | TCAGCAGTTGCTAAT[C/T]AGCATTATTACTGTC | 51429 |
| rs764981228 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157935681 | AGGTGTCATAATGGT[A/T]CTGCCTCATGTTTTA | 51429 |
| rs764981229 | snp | C/G | | | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822522 | TCCCCCAAACCTCTC[C/G]GGCCCTCCGGTATTT | 51429 |
| rs764998276 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157855650 | CTTTTCTTACTGACT[C/T]GTACTCTTTATATAG | 51429 |
| rs765034624 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157788890 | GTCTCAATTTCCTCA[-/T]TCCTCAAAATGGGGA | 51429 |
| rs765037134 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157743231 | TTTATTTGTATTTTC[A/G]GGTTTAGTTCTCTGT | 51429 |
| rs765051352 | in-del | -/TTC | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894570 | CTCTCTACTGGAATA[-/TTC]TTTGAGATTGGGTGC | 51429 |
| rs765066086 | snp | A/T | | | intron-variant, nc-transcript-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157885273 | TATAAATAGATTGAG[A/T]CTGCTGTGATCTACC | 51429 |
| rs765085161 | in-del | -/CT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157865145 | GAGTTTGAGACCAGC[-/CT]CTGACCAACATGGTG | 51429 |
| rs765089077 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157863000 | AGTTTGTCCTTCAAA[A/C]AGGACACTGTTTCTC | 51429 |
| rs765093538 | snp | A/G | 1.6476e-05 | 0.00287014 | missense | SNX9 | GRCh38.p7 | 6:157940901 | AGATGAATCACTTTC[A/G]CAGTAACCGGATCTA | 51429 |
| rs765130156 | snp | A/G | 1.64852e-05 | 0.00287094 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157927155 | GAGAGATGAGCTGGC[A/G]GGAGTCATGATATTT | 51429 |
| rs765134500 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157747119 | CTCACCTCCTGCTAT[C/G]CAGCCTGGTTCCTAA | 51429 |
| rs765137261 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157824828 | TTAATTTTGTGTTGA[A/C]CTTTTTAAAAATAAA | 51429 |
| rs765165334 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157832938 | AATACTTCCATAGTA[C/T]AGCTCCACAGTCTGC | 51429 |
| rs765181149 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157815666 | TAGGCGTGAAATAAG[A/C]AGCAGCTAATACACA | 51429 |
| rs765192089 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157915121 | GTATTTGTTGGTTTA[C/T]TTCTGGATTCTATTC | 51429 |
| rs765194657 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157856731 | GTAGTACCTTGATTT[C/T]TTACCTTACCCTCAT | 51429 |
| rs765196490 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157768061 | GTCTCAGGCCCAGGT[-/A]ACTTCCTCAGTCCCA | 51429 |
| rs765199294 | snp | A/G | 3.29946e-05 | 0.00406155 | missense | SNX9 | GRCh38.p7 | 6:157896836 | CAATAGGTTGGCAGT[A/G]GCAATGACCCCTGGT | 51429 |
| rs765211649 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157853818 | ACAACAAAGGTGGTG[A/T]TAGCCTGCATTTACT | 51429 |
| rs765232188 | snp | A/G | 3.72155e-05 | 0.00431351 | intron-variant | SNX9 | GRCh38.p7 | 6:157902079 | CAGGGAACCAGGGCC[A/G]TGGTAGAAGTATACA | 51429 |
| rs765234062 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157934437 | GGAAAAAAAATTTCT[A/T]ATCAAAAGCAAAATA | 51429 |
| rs765289677 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157739126 | CTAAAGAGCTTCTAC[A/G]CAGCAAAAGAAACTA | 51429 |
| rs765301114 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157795143 | TCTTGAGGCGGGGCA[C/T]GGTGGCTCATGCCTG | 51429 |
| rs765317246 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157800867 | AGTCCATTCTGTCTG[A/C]TCCATTGACCATGGA | 51429 |
| rs765319229 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157786496 | GAAAGTGGAATGGTT[C/T]CTATTTGTAGATAAC | 51429 |
| rs765326032 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157728598 | CCCCCTCAAGGTTAG[A/G]TTGTCCCTACCATTC | 51429 |
| rs765335972 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157934146 | CTGGAAATATTGTGA[-/T]TTATAGTAAAAATAA | 51429 |
| rs765338832 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157841058 | TATAAACTTCCTGAA[G/T]CCCCAGCAGTCTTGA | 51429 |
| rs765348779 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157761049 | TCACTAGTTACACTT[C/G]GTGGTGTACCAAGGA | 51429 |
| rs765359168 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157926194 | ACCATAAGAGAGAGA[-/T]TACCGGTTACCTTTG | 51429 |
| rs765366271 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157883036 | CATGGCAGACTTCAT[C/T]GTCTTGTTTTAAGAA | 51429 |
| rs765367523 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157922543 | TGTAGTAATTTTCAC[A/T]TGTTGAAGTGAACAC | 51429 |
| rs765394628 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157717703 | AGGAACTGAGGCTGA[A/G]CCGGGCGTGTTTAAG | 51429 |
| rs765409627 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157842073 | TATATCTCCAAAACT[C/G]TAGACTTAAATAACT | 51429 |
| rs765417684 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157911389 | GGGAAGACAAGAGGC[A/G]GTGGAATTCTCACTG | 51429 |
| rs765440161 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157814426 | CTGGAAAATGTACCT[A/G]TCTTTCAAGAAAGCT | 51429 |
| rs765455763 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157881937 | TATCCAGAAGATCTA[A/G]CAAAGATTATTGATG | 51429 |
| rs765457357 | snp | C/T | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894030 | TTGTTCATGAAATGG[C/T]ATTAGGGTGACCGAC | 51429 |
| rs765491935 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157841478 | CTACCTAGAGACCCA[G/T]GGGCCTTCATGGGGT | 51429 |
| rs765497503 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157828767 | GGTTTGAGACACTAC[A/G]CCTGGCCACATATTA | 51429 |
| rs765504096 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157910662 | CCCAAGAATCTTTTG[A/G]TAAGTAACCCATAGT | 51429 |
| rs765518226 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157901357 | CATGTAGTCCCGCCT[A/G]TTATTTTTGACTTTG | 51429 |
| rs765533046 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157729828 | TTCTTCCAATAAACT[C/G]AACATGAGGAACTTA | 51429 |
| rs765537405 | in-del | -/GT | 1.65018e-05 | 0.00287239 | frameshift-variant | SNX9 | GRCh38.p7 | 6:157921626 | ATCTCAGAAAGTGAA[-/GT]TTTCCAGCAGTTCCT | 51429 |
| rs765559137 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157847918 | GCCTCTGGCATTGTT[G/T]TGACCTGGCTTTACA | 51429 |
| rs765569933 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157773386 | ACATGTCCAGAGGCA[C/T]GTGGAAGAAGTCTGC | 51429 |
| rs765570046 | snp | C/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889813 | AGATGGGGATTTACT[C/G]AAAGAAATGCTAGTC | 51429 |
| rs765578764 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157860103 | GAAAATATTTACTAT[C/T]TGGTCCTGTACAGAA | 51429 |
| rs765587276 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157826413 | GCTGAGGCAGGAGAA[C/T]AGCGTGAACCCGGGA | 51429 |
| rs765590815 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157774141 | CGCAGCCCAGAGGGA[C/G]AGGACCCAATGGAAA | 51429 |
| rs765603590 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157814204 | CTATATGCCACTGCC[-/A]AATCTTCCAAAAACA | 51429 |
| rs765621011 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157769365 | GCAGGCGCAGGCACC[C/T]CCATCTTCGTGGACA | 51429 |
| rs765632369 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157937412 | TCTCTGCCAGTAACA[A/T]TCAGCTTGTATCTTG | 51429 |
| rs765644182 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157940448 | TGTTTGAGACAGTCT[C/T]GCTCTGTCACCCAGG | 51429 |
| rs765653948 | in-del | -/AAAAAAA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157932867 | GCAAGACCCTGTCTC[-/AAAAAAA]AAAAAAAAAAAAAAA | 51429 |
| rs765667549 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157836718 | GCCTCAGCCTCCCAA[G/T]TAGCTGGGACTACAG | 51429 |
| rs765681849 | snp | A/T | 3.36967e-05 | 0.00410454 | intron-variant | SNX9 | GRCh38.p7 | 6:157932146 | AAATAGTTTAATCCC[A/T]TTTCAGTTTGCTCAG | 51429 |
| rs765690543 | snp | C/T | 1.64936e-05 | 0.00287168 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157875149 | CACAGCTCAGGCCAG[C/T]TCGTCGGCTGCCAGC | 51429 |
| rs765695032 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157872392 | TTTTTCTGCATAACA[A/G]TCCTAAAACTTACTA | 51429 |
| rs765705183 | snp | C/T | 1.64855e-05 | 0.00287097 | intron-variant | SNX9 | GRCh38.p7 | 6:157910049 | GTGTAATGCTAAACC[C/T]AGGATGACAAATAGA | 51429 |
| rs765738672 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157770935 | AATTTGTGAATATAC[C/T]TATGCTTATATTTAT | 51429 |
| rs765755597 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157849326 | GGATACATGGTCAGC[C/T]TCTTTATAAGCCATG | 51429 |
| rs765760167 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157753748 | TCTGCTTCTGTAACC[A/G]CCCAAGGGGTTCACC | 51429 |
| rs765770627 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157877951 | TTTTAAAGATCTCTT[C/T]GAATAACTTATTTCG | 51429 |
| rs765795295 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157719038 | CCCAGCCACAACTCC[C/T]TGATGAGGCAGTGTG | 51429 |
| rs765815880 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157803606 | AAGGCGACTGAAACA[A/G]GACCAAGAGCATCAC | 51429 |
| rs765819442 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157918131 | TGTCAGTTAGGCTGG[A/G]TTGATAGTGTTATTC | 51429 |
| rs765828662 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157897040 | CCTGCCCGCCCATGG[C/T]TGAGTGGGAGAGACA | 51429 |
| rs765829842 | in-del | -/C | | | intron-variant, downstream-variant-500B | SNX9, LOC105378078 | GRCh38.p7 | 6:157884864 | CTATTAAAGCAAAGT[-/C]TTTTTTTTTAACCTT | 51429 |
| rs765848331 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157898011 | TTAGGAGATCTGTGT[C/T]AGGAGCCAGGGTCAG | 51429 |
| rs765861482 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157812071 | GACCTCCTCCAATGG[A/C]TGCCCGGATATCCTC | 51429 |
| rs765865488 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157868838 | GTAAAACTTGAACCC[A/G]TCGTTACCTGCTTTC | 51429 |
| rs765884845 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157936911 | AGATGACTTTAAACT[A/G]TGTGTATGGATGCAC | 51429 |
| rs765887047 | snp | C/T | 1.658e-05 | 0.00287919 | stop-gained | SNX9 | GRCh38.p7 | 6:157921650 | CAGTTCCTAAATTTC[C/T]GAGATGAGAAGGTAG | 51429 |
| rs765894778 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157761155 | TCTGCTTTCTATTAT[C/T]GCCATGTGTGGCGAT | 51429 |
| rs765897650 | in-del | -/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157762840 | GAGGCTTGCCCATGT[-/G]GGTTCCTCCAGTACC | 51429 |
| rs765908742 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157929403 | GCAGAGTGACTTGTC[A/C]GGCCCTGAAATGCTG | 51429 |
| rs765909870 | snp | C/T | 3.30109e-05 | 0.00406256 | intron-variant | SNX9 | GRCh38.p7 | 6:157896816 | CTCCTTCTTTTTACC[C/T]CTCTCAATAGGTTGG | 51429 |
| rs765957933 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157856911 | ATGCTTAGATGAATT[A/G]AATCTTTGGGGATTG | 51429 |
| rs765989922 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157831652 | GGGAAATCCTGCCTC[A/G]GCACATGTGTTCTCC | 51429 |
| rs765997346 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157927300 | AGTGTAGCCGCAGCC[A/G]AAACTCAAATCAGAC | 51429 |
| rs766010745 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157801206 | ACTGTTTCTACAGAC[A/G]GGCTTCTGATCTTCT | 51429 |
| rs766010940 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157754632 | GCGTGGACATCAGCA[-/C]GTCCTAAGTCTGCTC | 51429 |
| rs766026980 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157904615 | ACTTGGGAGACTGAG[A/G]CAGGATAATCGCTTG | 51429 |
| rs766039723 | snp | A/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886563 | TTGTATATAAATGGT[A/T]ATGGTTTACCACCAG | 51429 |
| rs766049097 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157918873 | CTATATAGCTTTATT[-/C]CCTTCCCTCATTTAT | 51429 |
| rs766060594 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157813311 | TGCAAACCCCAAAAG[G/T]TCATATTCTCTTCCC | 51429 |
| rs766064810 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157829458 | CTGTGCACAAAAAGA[A/G]TATACATATTATTGA | 51429 |
| rs766083106 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157926157 | CACATTCAAACCATA[A/G]CAGAAAAGCAAAGAA | 51429 |
| rs766088216 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157741277 | CACTGGAACCCAGGA[A/G]GTGGAGCTGCAATGA | 51429 |
| rs766089370 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157938235 | ATAAAATATTCTGTT[A/G]TATAAAAAAAGAGAG | 51429 |
| rs766092010 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157744905 | GTGTGCCACCACACC[C/T]GGCTAGTTTTTGTAT | 51429 |
| rs766092425 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157802071 | ATATTCTCAGAGAGG[C/T]GGATGTTCATTCAAG | 51429 |
| rs766114824 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157915194 | ACTGTCTTGACTTGT[A/G]TAGCTTTATGGTAAG | 51429 |
| rs766126015 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157864274 | AGCAGTGTTGATCCC[C/T]TCTTGAGGACAAAGC | 51429 |
| rs766131910 | snp | C/T | 1.6486e-05 | 0.00287102 | splice-donor-variant | SNX9 | GRCh38.p7 | 6:157938749 | TTACGCGTTGCAAGG[C/T]AAGATGAAAGGGTCC | 51429 |
| rs766178673 | in-del | -/TTTG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157765352 | ATATATTTGTTTTTT[-/TTTG]TTTGTTTGTTTGTTT | 51429 |
| rs766214199 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157875851 | GACAGGTATCAAAAT[A/G]TTGTTGCTGCTGGGC | 51429 |
| rs766215993 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157819489 | AGGTATCCCCTTGTG[C/T]CAGACCCAGGCTGAC | 51429 |
| rs766217526 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157776529 | TGGGGAAGAAACTCT[C/G]CCATCACATCTTGAA | 51429 |
| rs766257860 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157722543 | CTGTCTGTGCCTCCA[C/T]AGCCATTTTGCTCCA | 51429 |
| rs766258328 | in-del | -/TT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157730641 | TATGTCCCTTAGTTC[-/TT]TTTTTTTTTTTTTTT | 51429 |
| rs766264108 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157932468 | CCAAAGGTGGTTATA[A/G]TTTGTATTTTCTTGC | 51429 |
| rs766275716 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157761880 | CTGGGGAGGTTCAAT[A/G]TAGATTTAGGTCTGG | 51429 |
| rs766281454 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157721530 | TGATTGTCGTCTGCC[C/T]TGCTTACAATGCTAC | 51429 |
| rs766283554 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157820025 | CTGAACTTAGCATGG[C/T]CCAGGGTTCTGGGTT | 51429 |
| rs766287257 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157933240 | TCGAGGCTATAGTGT[C/G]CCATGATCACACCAC | 51429 |
| rs766290691 | in-del | -/CTCT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157922149 | AGAGTCAGTGCTGGC[-/CTCT]CTCTCTGCCTGCCCC | 51429 |
| rs766301214 | snp | A/G | 1.74866e-05 | 0.00295686 | intron-variant | SNX9 | GRCh38.p7 | 6:157902062 | TAAGTTTAAAGGGGA[A/G]CCAGGGAACCAGGGC | 51429 |
| rs766310994 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157912483 | AAAGCAAGAAAGCAG[C/T]AGCCCCTCGGTGTGA | 51429 |
| rs766346019 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157741813 | TCCTCAACCTCTGCA[A/G]CCAAAATAAGACTCT | 51429 |
| rs766354413 | in-del | -/ACTGTG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157841541 | GTTCCAGGAGGTCAC[-/ACTGTG]ACTGCACAGCCCATG | 51429 |
| rs766364117 | snp | A/G | 0.00029678 | 0.0121779 | intron-variant | SNX9 | GRCh38.p7 | 6:157928740 | ACTGGGCTCGTAGGG[A/G]GTGATGCAGGCTCAG | 51429 |
| rs766365591 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157752038 | TCTACTAAAAACACA[A/G]AAATAAGCTGGGCAT | 51429 |
| rs766413613 | snp | A/C | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157893176 | GGAAGGGTTTCTCTT[A/C]GCTGAAGTGTGACTG | 51429 |
| rs766428541 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157760649 | TGAGGGTACAGAGGA[C/T]ATGGGGACTGGGAGG | 51429 |
| rs766431677 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157759110 | CAATGATGGTGTTGA[C/G]AGTTTCAAAAGACAG | 51429 |
| rs766458084 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157817153 | GAGAAATAAACATTT[A/G]TCGTTAATAAGCCAC | 51429 |
| rs766478429 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157773409 | AAGTCTGCAGTGGGG[G/T]TGGAGGTAGGTAGCA | 51429 |
| rs766485508 | snp | C/T | 4.27095e-05 | 0.00462092 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157928647 | CAAGGCCATGGATGA[C/T]GGCGTGAAGGAGCTG | 51429 |
| rs766485837 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157797789 | TCACACTGGACAAAT[C/G]CAGGACAACTTGGCA | 51429 |
| rs766507903 | in-del | -/TT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157795448 | AAATTAAAACATATC[-/TT]AGGGATATTTTAGAA | 51429 |
| rs766518404 | in-del | -/AT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157874862 | TCGAGAAATTAAAAA[-/AT]AGTTTGAACTAAATA | 51429 |
| rs766519257 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157838831 | TCTAAAATTTTATCT[G/T]GCACTGGTTAAACTA | 51429 |
| rs766525075 | snp | A/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894731 | ACCCCTCAGCGTGAC[A/G]GTTGTCAGAATGTGG | 51429 |
| rs766530010 | in-del | -/AC | | | intron-variant | SNX9 | GRCh38.p7 | 6:157883722 | GCTCTTCTGAGAATA[-/AC]AGAGTGACTCCTTCC | 51429 |
| rs766544374 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157829777 | TTTTGGTAAATATTT[C/T]CCAGATATATAAAAG | 51429 |
| rs766546680 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157940535 | CAATTCTCCTGCCTC[A/G]GCCTCCCAAGTAGCT | 51429 |
| rs766556182 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157786175 | AGCCTCCCGAGTAGC[A/T]GGGATTACAGGCACT | 51429 |
| rs766586867 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157864143 | GGCAGGGTAGGGCCC[A/G]GCTCTGCTTCCAAGA | 51429 |
| rs766603634 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157908292 | ATTATTTCATTCTCC[A/T]TGAATCTCTGAATGA | 51429 |
| rs766621954 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157837037 | TAAGATCTGTGAGGC[C/T]GTAAATTGGGTGGCT | 51429 |
| rs766646203 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157785018 | TTGGGAGGCCGAGGC[A/G]GGCAGATCACGAGGT | 51429 |
| rs766653342 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157719080 | CCCACTCTGACCCCA[A/T]GCCCAGGTCCTGCCC | 51429 |
| rs766655726 | in-del | -/TGGC | 1.65919e-05 | 0.00288022 | intron-variant | SNX9 | GRCh38.p7 | 6:157875204 | TCCTCCTTCTGGATG[-/TGGC]TGGCTTTACGGAAAA | 51429 |
| rs766684262 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157748319 | GATATCTATGATAAA[C/T]ATTTCCTTTAAAATG | 51429 |
| rs766713856 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157727088 | AATCTGGGTATGGTG[A/G]AAGGAAGTGAATTAA | 51429 |
| rs766733040 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157850664 | AGAGCTCCCTTAAAC[A/G]AAAATTTGATAGTGG | 51429 |
| rs766749967 | snp | C/T | 1.64757e-05 | 0.00287012 | missense | SNX9 | GRCh38.p7 | 6:157901946 | GGGATGGGCCCAAAT[C/T]CTCTTCCTACTTTAA | 51429 |
| rs766756391 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157830099 | GTATTTTAGTTATAT[-/C]TTTTTCACCACAAAT | 51429 |
| rs766772447 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157916082 | CTCTGTCGCCCAGGC[A/T]GGAGTGCAGTGGCGC | 51429 |
| rs766776806 | snp | A/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157890581 | ACCTGTGGTGATTAC[A/G]TAGATTTAAGCGTGT | 51429 |
| rs766782231 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157755617 | ACTGATTTAAGCTTG[A/C]ATGTGAGAGATTTAA | 51429 |
| rs766785592 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157875549 | CTCGGCCTGGATCAG[A/G]AAATAGATGCCCTGG | 51429 |
| rs766807501 | snp | C/G | | | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822607 | CCCCACCGTCCCGTC[C/G]CAGGGGCTTCAAGCC | 51429 |
| rs766838452 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157932703 | GACCCCCATCTCTAC[-/A]AAAAAAATAAAAAAT | 51429 |
| rs766848756 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157774564 | CTTAGGAATGGCCCC[A/G]TCTGCAACAGACAGG | 51429 |
| rs766851237 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157771679 | CTGCCAGGGACATAT[C/G]CAGAGTGGGCTGGCT | 51429 |
| rs766879391 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157880172 | CCAGGCTTGCCAGTG[C/T]GGCTCCACTGTGTAA | 51429 |
| rs766899546 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157738234 | TCTAATATTGACAGT[G/T]GGGTGTTAAAGTCTC | 51429 |
| rs766900751 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157851466 | ACCATCCCAAATAGA[A/C]ACTCTGTATTGCATT | 51429 |
| rs766905673 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | SNX9, LOC107986663 | GRCh38.p7 | 6:157714952 | GGAGGCTGAGGCAGG[A/G]GAATTGCTAGAACCC | 51429 |
| rs766919266 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157873529 | GATATATGAAATTAT[A/T]TCTCAATATATCTGT | 51429 |
| rs766951083 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157804840 | GGATGTGAGCTGGAG[C/T]GTGGAGGGAGGGAGG | 51429 |
| rs766959412 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157920317 | GTTCAACCTTGGCTA[G/T]CAGGGCTGTTGTCCC | 51429 |
| rs766962221 | snp | C/G | 6.70882e-05 | 0.00579134 | intron-variant | SNX9 | GRCh38.p7 | 6:157875016 | TGAAGTGACCGTAAT[C/G]TATGAAAATAATTGC | 51429 |
| rs766989291 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157858511 | ACAAGTGTGAGCCAC[C/T]ATGCCCGGCCATTGT | 51429 |
| rs766989479 | in-del | -/TTTG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157836109 | GCTAATATTTAATTT[-/TTTG]TTTGTTTGTTTGTTT | 51429 |
| rs767000206 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157897134 | CAGCATGGGAAGGGA[A/G]GATTGCCCCACCCAC | 51429 |
| rs767007739 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157814356 | TGTCAGGGAAATGCA[A/G]CCTGAACTGCTTCCT | 51429 |
| rs767028654 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157793038 | GTAAGCTCCACCTCC[C/T]GGGTTCAAGCAATTC | 51429 |
| rs767037718 | snp | C/T | 8.2528e-05 | 0.00642318 | intron-variant | SNX9 | GRCh38.p7 | 6:157910076 | TAGAAAGACTCCAGT[C/T]AGATTATCTTCCTGT | 51429 |
| rs767043281 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157805570 | AATGTGCTGTGATCA[A/G]TGGAGCTGCCAGGTC | 51429 |
| rs767047300 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157919199 | CTTTATTTTTAGAGG[A/T]TAGTCGTACCGATCT | 51429 |
| rs767056341 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157772050 | AGGATGGGTTGGGGG[G/T]ACTCAAAAGGGCAAA | 51429 |
| rs767124318 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157916920 | GCAATGCTAGTCTCA[C/T]AGGATGAGTTTGGAA | 51429 |
| rs767125866 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157734828 | AGGGAAAGAAAAGAA[A/G]TTATATTTTCTCCCT | 51429 |
| rs767133241 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157722585 | TTTTAGCAAAGCGCT[C/T]CTCTGTCTTTCCTCG | 51429 |
| rs767146535 | snp | A/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894290 | AATTTTTGTATTTTT[A/G]GTAGAGATGGGGTTT | 51429 |
| rs767155236 | in-del | -/AA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157825760 | TTCTTGTGTCAAACC[-/AA]AGTCTCATTTTTTAA | 51429 |
| rs767156417 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157789369 | GGCTAGTCGATATTA[C/T]AGATTCAGGAGCCAT | 51429 |
| rs767161577 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157898900 | TGGGCTGGGTAGAAG[C/T]GTTGGGAGACTCCTG | 51429 |
| rs767174319 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157908091 | TTCCCATCTTCCTCT[G/T]AAAAAAAAAAATTAG | 51429 |
| rs767177385 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157851150 | GTAATCCCAGCTGCT[C/T]AGAAGGCTGAGGCAG | 51429 |
| rs767182101 | snp | A/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886819 | GTCTTTTTTTCTGAC[A/T]GTAGCATGGATGTAT | 51429 |
| rs767195216 | in-del | -/AAA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157753233 | TTTCTTTTTAGTGGC[-/AAA]AAAAAAAAAAAAAAA | 51429 |
| rs767217525 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157847509 | TGCTATATATTCTAT[A/G]GGAGTTTTCTTTCTG | 51429 |
| rs767228102 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157790526 | TACAAAGGATTGAGA[A/G]ACTGGCACACAACCC | 51429 |
| rs767241442 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157943753 | CACCCAGCACCCCGG[C/T]GTCTCTGGCCCTTTC | 51429 |
| rs767247201 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157921702 | CAGAGAATATTGAGA[A/G]TTGTCTCATTCACAC | 51429 |
| rs767259220 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157852834 | CCACCTCGGCCTCCA[A/G]AATGCTGGGGTTACA | 51429 |
| rs767262681 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157932373 | CTCCTCAGTGAAGCA[C/T]CCTGGTTGTGGGTGT | 51429 |
| rs767291465 | in-del | -/CCA | 0.000166138 | 0.0091127 | intron-variant | SNX9 | GRCh38.p7 | 6:157927224 | GAAATGTGAGAGACG[-/CCA]CTGCCAGGTTTTCTT | 51429 |
| rs767296104 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157742896 | TCCCTGAGTCCTACA[A/G]CTCTGACTTCTGGGG | 51429 |
| rs767298659 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157833238 | TTAGTTTGTTTTATA[A/G]TCTCAAGATTTTAAG | 51429 |
| rs767316983 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157721760 | GAGGTTCTTTCCCTC[C/T]TTCCCGCCCGTCCTG | 51429 |
| rs767322526 | in-del | -/A | 1.66182e-05 | 0.0028825 | intron-variant | SNX9 | GRCh38.p7 | 6:157942751 | TGAGGTCGTAATGGG[-/A]GTGATATCTCAACGT | 51429 |
| rs767379306 | in-del | -/AT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157818105 | CACACACACACACAT[-/AT]ATATATATACATATA | 51429 |
| rs767409235 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157820127 | GAAGAGAGATATGCA[C/T]GGTTGATCAAGTGGG | 51429 |
| rs767413446 | snp | A/T | 1.64757e-05 | 0.00287012 | missense | SNX9 | GRCh38.p7 | 6:157901922 | ATGATGATGACTGGG[A/T]TGAAGACTGGGATGG | 51429 |
| rs767414978 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157919565 | TGATTCTTTTTTGGT[A/G]ACTTCTCTCTCCTTT | 51429 |
| rs767437605 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157944563 | TTGTGTGTGATTTTT[A/G]TTGTTGTTGTTAAGT | 51429 |
| rs767437778 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157933508 | TCCCACATGGCAATA[A/G]TTCTCATTGCCCTGG | 51429 |
| rs767477239 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157777816 | TGGAGTGGTAGGAAC[A/G]GCTAAGTGGTGCTCC | 51429 |
| rs767500319 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157730202 | ATCTTAGTATAACTG[-/T]TTTTTTTTTTTTAAA | 51429 |
| rs767537530 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157757004 | TTATCTCACACATCA[C/T]TGCACTGAATTCCAC | 51429 |
| rs767548338 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157917173 | GGTATAGTTTTAGAG[-/T]TGCTCATAGTATTTC | 51429 |
| rs767556473 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157866472 | CCAGCTACTGGGGAG[G/T]CTGAGGTGGGAGGAT | 51429 |
| rs767585703 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157805877 | GCTTTGTTGAGTGCC[C/T]ATCCTCTGTCAGGCA | 51429 |
| rs767604822 | snp | C/T | 1.81069e-05 | 0.00300884 | intron-variant | SNX9 | GRCh38.p7 | 6:157873099 | TTTTTGGTGACTTAT[C/T]AGGATGTAGGTGGAG | 51429 |
| rs767607292 | snp | C/G | | | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821175 | CAGGGTTATGAAATT[C/G]TTCTGGTGGGAAAAG | 51429 |
| rs767610353 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157919343 | TCTGGGATTCTCATT[A/G]CAAGTGTTTGGTGTG | 51429 |
| rs767620452 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157800879 | CTGCTCCATTGACCA[C/T]GGAAGCCCACGTCTC | 51429 |
| rs767624376 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157817260 | CTGCTCAAGTTCACA[C/G]AGGTGACAAGCAGCA | 51429 |
| rs767626666 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157858769 | AGGAGAAGCAAAGGG[A/T]CATCTTACATGGCAG | 51429 |
| rs767628749 | in-del | -/TTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157871774 | TTCTTCAGTCTTACC[-/TTT]TTTTTTTTTTTTTTT | 51429 |
| rs767631079 | snp | A/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157891837 | ATAGTGTGAGGAACA[A/G]CAGAGATGTAGAAAA | 51429 |
| rs767640770 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157725926 | AAGAACCTGAGTGCC[A/G]AGAGGACAGGGGTTT | 51429 |
| rs767646525 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157786340 | AGGCATGAGCCACCA[C/T]GCCTGGCCGATCCTT | 51429 |
| rs767664663 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157862753 | TAGGATCTAGTTTTT[C/T]GGTTTTCATTTTTGC | 51429 |
| rs767674078 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157719831 | TGAGGTCAGGAGTTC[A/G]AGACCATCCTGACCA | 51429 |
| rs767680839 | snp | C/T | 3.29989e-05 | 0.00406182 | missense | SNX9 | GRCh38.p7 | 6:157927192 | ATGGAACCAGAGGCA[C/T]CTGACTTGGACTTAG | 51429 |
| rs767681465 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157861359 | ATCCCCTTGGAGCTT[C/T]TTATCTGGTGCAGCT | 51429 |
| rs767683484 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157874090 | TCCAGGAGAAAAGAA[A/T]TCCCCCCAGAGGATG | 51429 |
| rs767697689 | snp | A/G | 0.000100125 | 0.00707478 | intron-variant | SNX9 | GRCh38.p7 | 6:157941019 | GTGCTTGAGGAGAGG[A/G]TTCCTGGTAAACCAC | 51429 |
| rs767725153 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157770562 | GGAGGCCAAGGCGGG[C/T]AGATCACGAGGTCAG | 51429 |
| rs767735697 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157880456 | CTTTGATTTGCCCAA[C/T]TTCTAGCTTTTTGTT | 51429 |
| rs767759700 | snp | A/C/T | 3.62111e-05 | 0.00425493 | intron-variant | SNX9 | GRCh38.p7 | 6:157906259 | CTGATTAAGCTCTTT[A/C/T]TTATACCGTACTTTA | 51429 |
| rs767805810 | snp | C/T | 2.51373e-05 | 0.00354514 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157928617 | GCAGAAGTGCGAGGC[C/T]GTGGGGAAGTTCACC | 51429 |
| rs767818610 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157804872 | GCCCGCCTTTACTGC[A/G]GTAGGGAGGAGCAGT | 51429 |
| rs767818680 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157798896 | AAATACATTCAGAAC[C/T]AGTTGGTTCTCTGTA | 51429 |
| rs767819215 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157869088 | CATGCCAGTGTTTCT[C/T]ACTGAATGTTTCCAG | 51429 |
| rs767819999 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157939629 | CTTTCAAGACTGGGG[C/T]ATTCATGGGAGAAAG | 51429 |
| rs767831576 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157736390 | CTTTAAGTGGTATTC[C/T]GAAGTATTTTATTCT | 51429 |
| rs767833955 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157838378 | TAAGTGAAAATGCAT[A/G]TATATTTTTCTATCC | 51429 |
| rs767850101 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157825759 | ATTCTTGTGTCAAAC[C/T]AAAGTCTCATTTTTT | 51429 |
| rs767861600 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157850708 | AGCTCCATACATCTG[A/T]TAATGCTTGGTGACT | 51429 |
| rs767863532 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157863677 | GTTGGGGTTGAGGCC[A/G]GCACCTCTGTCTGTT | 51429 |
| rs767864437 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157727445 | GTGAGGGCCCCAGTA[C/T]CTTCAAGGCCTGTCT | 51429 |
| rs767866384 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157938268 | AGTGCCTGTGTGCAC[A/G]TGCTGCCCTGTACCT | 51429 |
| rs767880945 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157910476 | CTGGACAGAGAAGCC[A/G]CAGAACTACTAAGTG | 51429 |
| rs767881582 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157910136 | GAGCAGCAGGATGCA[C/G]GAGTTGGAAACAGTA | 51429 |
| rs767898466 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157839659 | GAAGCAGACCTATAA[C/T]ATTTTAGTTCCCAGG | 51429 |
| rs767907820 | in-del | -/AT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157902813 | GCTGGGATTACAAAC[-/AT]GTGCCACCGCGCCCA | 51429 |
| rs767912631 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157937852 | GGCTGGTCTGTGATC[G/T]TAACAGTCCTGGCAT | 51429 |
| rs767914991 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157716610 | TGCTTTTAGCATGAG[C/T]GATTTTACTTTGAAA | 51429 |
| rs767929469 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157745958 | ATTTTCAATCCTGTT[G/T]TGTAAACACATTACA | 51429 |
| rs767960343 | in-del | -/TTTTT | | | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821598 | GTGTCACATATTTCC[-/TTTTT]TTTTTTTTTTTTACA | 51429 |
| rs767969709 | in-del | -/AG | | | intron-variant | SNX9 | GRCh38.p7 | 6:157926764 | CAGCCTAGAAGGCAA[-/AG]AGTGAGACTCTGTCT | 51429 |
| rs767982992 | snp | A/G | 6.59707e-05 | 0.00574291 | missense | SNX9 | GRCh38.p7 | 6:157901997 | CAGGCGGCGCTCAGC[A/G]AGGAAACAGTCGTGC | 51429 |
| rs767983583 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157767158 | ACTGTCTCATCTTTG[A/G]TACTCAGCTGGAGGT | 51429 |
| rs767993251 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157770862 | TAGGATGCCTGAGTC[G/T]CATGCTAAACAAAAT | 51429 |
| rs768004609 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157813807 | GGTCCTTTCAAAGTT[A/C]CTTTCCTTGTAAAGA | 51429 |
| rs768011631 | in-del | -/TGT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157804555 | GACCCAGGGAAGAGA[-/TGT]TGTTGGAGTCTGAAA | 51429 |
| rs768014001 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157869906 | ACACATGCGCACACA[C/T]CTCGCACCCTCATAC | 51429 |
| rs768050983 | snp | A/C/T | 5.07982e-05 | 0.00503954 | intron-variant | SNX9 | GRCh38.p7 | 6:157867665 | TTCGAGTCTGATTGT[A/C/T]CCATGTGGACTTATT | 51429 |
| rs768059370 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157851927 | TATTTCAATTAGCGT[A/G]ATGTTTTCAAGGTTC | 51429 |
| rs768072363 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157857088 | AAATGAATTCATTTC[C/G]TACCATTCTATAATG | 51429 |
| rs768105039 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157825109 | AGAAATTAGCTGGGC[A/G]TGGTGGCGCGCGCCT | 51429 |
| rs768106994 | in-del | -/GAC | 5.8793e-05 | 0.00542153 | intron-variant | SNX9 | GRCh38.p7 | 6:157873092 | TTTTTTTTTTTTGGT[-/GAC]TTATTAGGATGTAGG | 51429 |
| rs768109115 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157909757 | CAAAATGTATGGTCT[A/G]AAGAGCTACATCGAA | 51429 |
| rs768110990 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157728331 | CAACTTCAGTTGACA[G/T]GTCAATTAAGTATGA | 51429 |
| rs768113461 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157838722 | CATGTTTAGTTTGAG[A/G]TCTCATTTAAAGAGC | 51429 |
| rs768131025 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157898106 | TAGGAGCTCTGTGCC[A/G]GGAACTAGGGACGCA | 51429 |
| rs768141449 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157916763 | CCAGCCTTACATGCC[C/T]GGAATAAACCTCACT | 51429 |
| rs768148493 | snp | A/G | 1.64757e-05 | 0.00287012 | missense | SNX9 | GRCh38.p7 | 6:157938694 | GTAAAATCACCCTAC[A/G]AGACAAACAGAACAT | 51429 |
| rs768201272 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157725267 | TGTGATGTGTCTCGT[A/G]GTTTTCTTCATGTTT | 51429 |
| rs768205834 | snp | A/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157891101 | TAGTGGTGTGAACTC[A/G]GCTCACTGCAACCTC | 51429 |
| rs768224444 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157861217 | CTGTTAAAATGTTCT[A/G]TCATCTTGACTATAC | 51429 |
| rs768231782 | snp | A/G | 1.64904e-05 | 0.00287139 | splice-acceptor-variant | SNX9 | GRCh38.p7 | 6:157901896 | TCCATTTTCACCTCT[A/G]GCAACTGGTGATGAT | 51429 |
| rs768244996 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157748913 | GTTATTAAAATCACA[A/G]TAACAATAGCATGGC | 51429 |
| rs768250480 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157930274 | AGACATCAGGAATAA[C/T]AGTTGTTTCTTTCCC | 51429 |
| rs768289796 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157806179 | AAATTGAGCTACTCT[A/G]TAAATTCTCATCATT | 51429 |
| rs768328555 | snp | C/G | | | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157822326 | AAAAGCACTCCACTA[C/G]TATGCCAATTAAGAC | 51429 |
| rs768332921 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157850311 | TGAGTAGCAGATGAA[A/G]TAGACCCGGGGCATG | 51429 |
| rs768334834 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157750527 | GTAAAACTCCTAGAA[A/G]AAAGATAGAGGAAAA | 51429 |
| rs768364882 | snp | A/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894369 | CCCGCCTCGGCCTCC[A/G]AAAGTGGTAGGATTA | 51429 |
| rs768373535 | snp | A/G | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886787 | TACAAATAGTGACCA[A/G]TGAAGAAAGCATTCC | 51429 |
| rs768374008 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157754587 | ACGTGCGTCACACAT[C/T]GTATGAACTGAGCAA | 51429 |
| rs768375701 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157730452 | AATCGCTTGAACCTG[A/G]GAGGCAGAGGTTGCA | 51429 |
| rs768377909 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157909367 | TTGAGACAGCTAGAC[C/T]AGAAAGAAACATTGT | 51429 |
| rs768399229 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157737209 | TTCTATTGATTGGAA[G/T]AGTTTCAGAAGGAGT | 51429 |
| rs768408195 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157726527 | GTAATTTTTTATTAG[A/C]TGTCAGACATTAGGG | 51429 |
| rs768427440 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157878967 | TACTTGGGAAAATGC[C/T]CATTTTAAGATTCTT | 51429 |
| rs768436874 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157755296 | GGAGTTGCTCTGGTT[C/T]GCATGCCTCTGACAC | 51429 |
| rs768455310 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157937799 | AGTCTATCGTATATT[A/G]TGATGTACTTGGATT | 51429 |
| rs768463586 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157908698 | TGGGACAGCAGACCT[A/G]TTGTCACCTAGCAGT | 51429 |
| rs768466689 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157716258 | AGGCTGCCTCCAACC[C/T]AGACACTAGGAAACA | 51429 |
| rs768469837 | snp | C/T | 1.73246e-05 | 0.00294312 | intron-variant | SNX9 | GRCh38.p7 | 6:157873219 | AGAGCTCATCTTTGC[C/T]AGGCATCTTTTTATG | 51429 |
| rs768489615 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157745548 | GTAATTTGCGGAGCC[A/G]AGAAAAGAAGACTTG | 51429 |
| rs768515844 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157770635 | TACTAAAAAAAAATA[A/G]TAATAATACAAAAAA | 51429 |
| rs768519727 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157855332 | CTTTTGCTATTCTGG[A/G]TGGCATTGCAGTAAA | 51429 |
| rs768521987 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157920059 | CTGACAGAGGTTGTA[C/G]CCAACCACCTCAGGC | 51429 |
| rs768522623 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157744330 | ACCGCAAATGAGCCA[C/T]AGTTTAAGAGGCTCT | 51429 |
| rs768570091 | snp | G/T | 1.65045e-05 | 0.00287263 | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157942876 | ATGCCGCGTGCTTTC[G/T]CCTGACTTGGGGCAA | 51429 |
| rs768575574 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157823983 | ACCGAGGCTGGGACG[C/T]CCCGCGCCCCTTTGC | 51429 |
| rs768587893 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157864872 | GTCTCTACCAAAAAT[A/G]CAAAAATTAGCTGGG | 51429 |
| rs768590310 | snp | G/T | 3.30104e-05 | 0.00406252 | missense | SNX9 | GRCh38.p7 | 6:157942819 | TGAGGCAGGCCCTCA[G/T]CCGCTTTCCAGTGAT | 51429 |
| rs768603512 | in-del | -/CACT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157870756 | TGCACACCCCTCAGA[-/CACT]CACCTGCTCTCACAC | 51429 |
| rs768606134 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157730395 | CCGGGTGTGGTGGTA[G/T]GCGCCTGTAGTCCCA | 51429 |
| rs768624709 | snp | C/T | 1.90264e-05 | 0.00308429 | intron-variant | SNX9 | GRCh38.p7 | 6:157936080 | AATTAAGATTTGTTG[C/T]TATCTAGTCCACATA | 51429 |
| rs768630973 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157943409 | TTCAAGAGGGAGGAC[G/T]CTGGGGGCCCCTGGG | 51429 |
| rs768635207 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157802824 | GGCCCCCCCGAACTT[G/T]CCAGTAGAATACCTG | 51429 |
| rs768650159 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157793521 | CATCTCATATTCCTG[A/G]TCTTTTAAAAAAAGA | 51429 |
| rs768674224 | snp | C/T | | | utr-variant-5-prime | SNX9 | GRCh38.p7 | 6:157766394 | CCCCAGACCATGTTC[C/T]GTGCTCCCCACCTTG | 51429 |
| rs768675626 | snp | A/C/T | 4.18419e-05 | 0.00457375 | intron-variant | SNX9 | GRCh38.p7 | 6:157928733 | ACAGTGCACTGGGCT[A/C/T]GTAGGGGGTGATGCA | 51429 |
| rs768698778 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157909379 | GACTAGAAAGAAACA[C/T]TGTCTTGTAACCAGC | 51429 |
| rs768715969 | snp | A/G | 1.64743e-05 | 0.00287 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157909736 | AGCAGATCCCAGGAA[A/G]GGCTCCAAAATGTAT | 51429 |
| rs768739508 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157869499 | TCAGTGAACCAAGGC[C/G]CCCAAGGCTAAGTCA | 51429 |
| rs768769440 | snp | C/T | 1.65102e-05 | 0.00287312 | intron-variant | SNX9 | GRCh38.p7 | 6:157937536 | AAGGTAACCTGATCG[C/T]AGACATTTATAGAAG | 51429 |
| rs768778295 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157723510 | TTCCACAGCAAACTC[A/G]GTTTCTTGTCATTTA | 51429 |
| rs768783209 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157876505 | TAAGTTTATCACCAT[A/G]TACTAACTGCAGGTT | 51429 |
| rs768790852 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157746144 | TCCAGGAATCAAATG[C/T]CCTGGAAGTGACTTT | 51429 |
| rs768791070 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157905751 | AGAAATGCCAGCATG[C/T]GGCTATTGCCCCCTG | 51429 |
| rs768823999 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157762500 | ATCATGTATATTTAA[C/T]ATGCACATGGAACAA | 51429 |
| rs768824187 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157808617 | AACATGTTTTCTTTG[C/T]CATATAGCTTGATAT | 51429 |
| rs768849391 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157911078 | AGATTGCGCCACCGC[A/G]CTCCAGCCCAGGCGA | 51429 |
| rs768891787 | in-del | -/GTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157789700 | GTACTTCTTCATAGA[-/GTT]GTTGTATTAAATGAG | 51429 |
| rs768914135 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157819646 | AAGCATTTAGTTGGG[A/C]TCTGAGCTCTTAAAA | 51429 |
| rs768917450 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157742637 | ACTTGGATGATCGAG[G/T]GGATTTAGGAACCAC | 51429 |
| rs768931540 | in-del | -/C | 4.60575e-05 | 0.00479861 | intron-variant | SNX9 | GRCh38.p7 | 6:157873077 | AATCTTTTTCTTTTT[-/C]TTTTTTTTTTTGGTG | 51429 |
| rs768954865 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157924709 | CTGAAATGGCATCAC[A/G]TGCCACCACAGTTCC | 51429 |
| rs768983140 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157907192 | TTCTCTGGACTTAAT[A/C]AAAATTGAACATGTA | 51429 |
| rs768985833 | snp | C/T | | | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157944377 | TCTTCTATAAAATCC[C/T]ATAGAACAATGTTTA | 51429 |
| rs768990720 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157813412 | CTGGGTTTGAAAGCC[-/A]AAAAAGATCAGGAGG | 51429 |
| rs768996507 | snp | G/T | 1.65274e-05 | 0.00287462 | missense | SNX9 | GRCh38.p7 | 6:157896902 | AGCTCAGAAGGCTGG[G/T]GGGCCCAGCCAGAGG | 51429 |
| rs769020862 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157916541 | AGTCTTTCACCATTA[A/C]CTATGATGTTAGCTG | 51429 |
| rs769037613 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157941872 | CCTAAGCCCTGTCCT[-/C]CCTTACAGGACGTGG | 51429 |
| rs769040285 | in-del | -/GTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157825849 | CCCCACACCTGAGTA[-/GTT]GTGTTTTTTCTTTGT | 51429 |
| rs769042850 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157923613 | AATAAAGATGTCATA[A/T]GTAGAAAATCAAAAT | 51429 |
| rs769066333 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157724276 | CGCCCAGCACTTCAG[C/T]GTGTTCACAACCCCA | 51429 |
| rs769086330 | snp | C/T | 1.64874e-05 | 0.00287113 | synonymous-codon | SNX9 | GRCh38.p7 | 6:157927137 | TGGAAAGAGGAAGGC[C/T]GAGAGAGATGAGCTG | 51429 |
| rs769099121 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157769759 | GGAGGCCCATGTGGA[C/G]AGGCAGTGGAAGGGG | 51429 |
| rs769105576 | snp | G/T | | | utr-variant-3-prime | SNX9 | GRCh38.p7 | 6:157943213 | TCCCACAATCTTCCA[G/T]TTCTTACCCAGTGTC | 51429 |
| rs769118109 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157718584 | AAAAATAAAAGCTAG[A/G]TTGGTTTGGTGTAAT | 51429 |
| rs769120720 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157863134 | CCAACTCCCATACCA[A/G]AGAGCTCTGAGAAAG | 51429 |
| rs769174176 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157769328 | CAACAATCAACAAAT[G/T]TTTGCAGAGTTCTAC | 51429 |
| rs769177169 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157840894 | GACCATTTGGCTGTT[-/A]ACCGTTATGCTGTTC | 51429 |
| rs769178676 | snp | C/T | 4.87472e-05 | 0.00493672 | missense | SNX9 | GRCh38.p7 | 6:157928681 | ACGGTGGGGCAGGAG[C/T]ACTGGAAGCGCTGCA | 51429 |
| rs769180081 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157799092 | TCTTCACAAGGCAGC[A/G]GGAGGGAGGGTGTGC | 51429 |
| rs769181235 | snp | A/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894805 | ATCGGTTCTAAATAC[A/G]CAGTCTCCTTAAGCC | 51429 |
| rs769204497 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157758594 | TGGGCAGGAAGAAGA[A/C]CAGATCAAATCTACC | 51429 |
| rs769205870 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157719597 | AACTCAATTAGATGC[A/G]AAATGTGCTTAGAAG | 51429 |
| rs769209013 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157884532 | ATCTCGTAATTGCTT[A/C]TTGAGACTTTCTCTT | 51429 |
| rs769229031 | snp | A/C | 3.47705e-05 | 0.00416942 | missense | SNX9 | GRCh38.p7 | 6:157896990 | ACCCCCAGGCCTACC[A/C]AGGACCAGGTGAGGA | 51429 |
| rs769234635 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157940391 | GTCATTCATTTACTG[C/G]AAAGTAATGTTTGTC | 51429 |
| rs769250428 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157716330 | CATGCCGGCCATCAC[A/G]TTTTAAGCAACTACT | 51429 |
| rs769271542 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157728106 | GGCCAGTTAGGGCAG[A/C]GAGGTGCAAGCTGGG | 51429 |
| rs769274532 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157824668 | TGAATCCATCTAGGT[C/G]CAGCGTTTGTAGAGA | 51429 |
| rs769309138 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157879935 | AGTTCTGTAAACCTA[A/G]ATGTCTTATCTGAAG | 51429 |
| rs769319570 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157837931 | ATACATGTAATTGTT[A/G]GCTGTGGTTAACATT | 51429 |
| rs769323838 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157909513 | TAACAGGAACAGAAA[C/T]CATTGAACCATTTAT | 51429 |
| rs769326545 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157842663 | CTTAAGGGGTTGAAG[G/T]TAGGTTTTCTTAATG | 51429 |
| rs769362759 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157778882 | GTATGAGTATGAGTA[C/T]GTTGTAGAGGATCAA | 51429 |
| rs769372434 | snp | A/G | 5.15504e-05 | 0.00507667 | intron-variant | SNX9 | GRCh38.p7 | 6:157928578 | CCTGCTTATGTGACT[A/G]ACGGCCGCCTTCACC | 51429 |
| rs769376115 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157738641 | AGCCCATATGGTAAA[G/T]ATAACCCTAAGAAAA | 51429 |
| rs769384674 | snp | C/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157891388 | TGTGATCGACCACAA[C/G]AAGTTAATTTTTTCA | 51429 |
| rs769405631 | snp | C/T | 8.14714e-05 | 0.00638193 | intron-variant | SNX9 | GRCh38.p7 | 6:157873085 | TTCTTTTTTTTTTTT[C/T]TTTGGTGACTTATTA | 51429 |
| rs769425138 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157916319 | GATTACAGGCGTGAG[A/C]CACCGTGCCCGGCCC | 51429 |
| rs769433035 | in-del | -/TTT | 0.0210705 | 0.100455 | intron-variant | SNX9 | GRCh38.p7 | 6:157873073 | ACTGTAATCTTTTTC[-/TTT]TTTTTTTTTTTTTGG | 51429 |
| rs769436642 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157756316 | TACTTGGGGGGCTGA[A/G]GCAGGAGGATTGCTT | 51429 |
| rs769436827 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157818636 | GCCTGTCCTTAACAG[A/G]TCAAAGAATTAAAAC | 51429 |
| rs769436908 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157805351 | TGGACTCTTACCTGA[A/C]CCTCCTGGTTGCTCT | 51429 |
| rs769456159 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157775610 | TTTTTCCCCCAATTG[C/T]TTTTTACACTTGAAA | 51429 |
| rs769463503 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157931590 | GAAATCATCTCTTCA[C/T]GCAGATGAGAAAACT | 51429 |
| rs769464000 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157727042 | CAGTGAAAAAAGAGA[G/T]CCAAAATGGTCTGTG | 51429 |
| rs769467786 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157839460 | AGCCTGGGTTCAAAT[C/T]CCAGTCCAGTTATTA | 51429 |
| rs769478407 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157838318 | GTGCTCGACCAATAA[-/T]TTTTTTTTTTTTTAT | 51429 |
| rs769482285 | snp | G/T | 1.65285e-05 | 0.00287471 | intron-variant | SNX9 | GRCh38.p7 | 6:157901878 | TTTTTTAACTGATGA[G/T]CTTCCATTTTCACCT | 51429 |
| rs769550143 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157766574 | TTAACTCTGGATGAT[C/T]GTACCCCATAGAACC | 51429 |
| rs769550447 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157792811 | TGTTAATTATTTAAA[A/G]TATTTAGTGTGTTTG | 51429 |
| rs769553156 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157874346 | TACTTGTATGCACTT[C/T]GCATCCAGGAGCCCA | 51429 |
| rs769561601 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157847119 | TGCAGGTTTTTGTTT[C/T]TGAGACAGGGTCTGG | 51429 |
| rs769562023 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157921475 | TCAGTTACAGTATGG[G/T]AACAGTCATTCATTT | 51429 |
| rs769569238 | in-del | -/TTTG | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157886861 | GATTTCATAATGTGT[-/TTTG]TTTTTTTTTTCTTTG | 51429 |
| rs769583756 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157928189 | TCTTTAGGATCACTT[A/G]GGTGATTGTGTATCC | 51429 |
| rs769587350 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157761826 | GCTTCAGTTCCTCAG[A/G]ATTCAAGAAGGGGGA | 51429 |
| rs769589317 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157772435 | GAAGAAAAGAAAATG[A/G]GGGCCAAACACAGGG | 51429 |
| rs769644169 | in-del | -/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157718684 | TCATAAACGTCTAGT[-/C]CCCTTAGGGATCCTA | 51429 |
| rs769675020 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157910126 | CCATCCTGTAGAGCA[G/T]CAGGATGCAGGAGTT | 51429 |
| rs769693016 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157858325 | AATCTCGGCTCACCG[C/T]AGCCTCCACCACCCG | 51429 |
| rs769723604 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157847438 | AGACCAAGAAAAATG[A/T]TGAGGCTAAAGTTTT | 51429 |
| rs769724222 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157824388 | TAACTGATCTGTGAT[-/A]ACACTGTGAGGAGTG | 51429 |
| rs769734354 | snp | C/T | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157887458 | GTCTCCAGAGCTCTC[C/T]CTCTGCGTCTCTGTC | 51429 |
| rs769748342 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157895869 | CAAACTGAAACTTGA[A/G]GGAAGCAGATAGGTC | 51429 |
| rs769802437 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157845886 | TTGTTCTTTACTCTT[A/C]TAACTTGATTGACTC | 51429 |
| rs769813335 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157907475 | TTTTATAGTAGAGAC[A/G]GGGTTTCACCATATT | 51429 |
| rs769823228 | snp | A/G | 1.67525e-05 | 0.00289413 | intron-variant | SNX9 | GRCh38.p7 | 6:157873179 | AGACTACGTTGAAGT[A/G]AGAGCTTCCTGTCAT | 51429 |
| rs769837145 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157782864 | GCAGTCCAGCCTGGC[A/G]ACAGAGTGAGACTAT | 51429 |
| rs769846667 | snp | C/T | 2.28626e-05 | 0.00338095 | intron-variant | SNX9 | GRCh38.p7 | 6:157935931 | AGAAAATATGCATAA[C/T]TTATAACCACTGATA | 51429 |
| rs769877287 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157844751 | GGCACCCGCCACCAC[A/G]CCCGGCTAATTTTTT | 51429 |
| rs769878043 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157908307 | TTGAATCTCTGAATG[A/G]ATCTCTGAGTGAATC | 51429 |
| rs769895220 | in-del | -/TT | 6.76653e-05 | 0.00581619 | intron-variant | SNX9 | GRCh38.p7 | 6:157938785 | AGGTGCTGGTGGAAG[-/TT]TTTTTTTCCCCAGCA | 51429 |
| rs769895986 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157746522 | AAGTATCAAGGGGCC[A/G]TATTTCTGCCCAATG | 51429 |
| rs769906432 | in-del | -/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157733965 | AAGACATGACAATCG[-/T]CACCCTTGGAAAGAA | 51429 |
| rs769931718 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157865994 | CCTAGGCGCATGTGA[C/T]CCCCAGTTTATAGGA | 51429 |
| rs769950963 | in-del | -/ATA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157740096 | AGAACTTAAAGTATA[-/ATA]ATAATAATAATAATA | 51429 |
| rs769951140 | snp | A/G | | | intron-variant, upstream-variant-2KB | SNX9, LOC105378078 | GRCh38.p7 | 6:157894895 | ACCACCAGGATGGCT[A/G]ATTAATAGAAAGGAG | 51429 |
| rs769952629 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157742832 | ATACACATTACATTA[C/T]ACATATGTAATGTAA | 51429 |
| rs769963193 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157810080 | CTATCGAGGAGTAAA[C/T]GAATAAACAAATTGT | 51429 |
| rs769964618 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157797463 | GATACATATGTGGTT[G/T]TATGTGTGTGTGTAG | 51429 |
| rs769979517 | in-del | AAAA/TTTTT | | | intron-variant | SNX9 | GRCh38.p7 | 6:157730210 | ATAACTGTTTTTTTT[AAAA/TTTTT]AAAAAAAAAAAAAAA | 51429 |
| rs769992534 | snp | C/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157868381 | TTCAGATGTGTGTCT[C/G]TGCTTATATAACTGG | 51429 |
| rs770002190 | snp | C/T | | | downstream-variant-500B | SNX9 | GRCh38.p7 | 6:157945480 | ACTCGTGGGTCTACT[C/T]ACATAGAGAAGAGAC | 51429 |
| rs770021391 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157811619 | TAATGGAGGTCACTA[A/G]ACTACAAACTTTGTG | 51429 |
| rs770024006 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157855132 | TGCATGTACTGCATC[A/G]CTGGGCCCTCTTTCT | 51429 |
| rs770024757 | snp | A/G | 1.65162e-05 | 0.00287365 | missense | SNX9 | GRCh38.p7 | 6:157896885 | AATCTGGGAACTGGG[A/G]AAGCTCAGAAGGCTG | 51429 |
| rs770053338 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157750628 | ACATCCAACTAGAAA[G/T]CTTCTGCACAGCAAA | 51429 |
| rs770058628 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157763715 | TGTCTGTCCTATTGA[C/T]GATTCCTCAAAACAC | 51429 |
| rs770074202 | in-del | -/A | | | intron-variant | SNX9 | GRCh38.p7 | 6:157777378 | AGCGAGACTCCATTT[-/A]AAAAAAAAAAAAAAA | 51429 |
| rs770077003 | in-del | -/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157905698 | ACAGTTGTGGCCTCT[-/G]GAGAGAGCCTGTTGA | 51429 |
| rs770077847 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157774038 | CTGGACTGAACAGAC[A/G]AGAGCCAACTTGAGA | 51429 |
| rs770089865 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157801950 | AGGTTGCCAAGCCCA[A/G]AGCATCCACAATATT | 51429 |
| rs770092630 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157720875 | GTTCAAGACCAGCCT[A/G]GTTGACATAGCAAGA | 51429 |
| rs770106979 | snp | A/G | | | upstream-variant-2KB, intron-variant | SNX9 | GRCh38.p7 | 6:157821948 | TCTTCTTTGTAAACA[A/G]TGGACAATAATGAGT | 51429 |
| rs770107167 | snp | C/G | 1.66399e-05 | 0.00288438 | missense | SNX9 | GRCh38.p7 | 6:157906204 | CCCAAAGAGAAAATT[C/G]CCATCATTGTAAGTT | 51429 |
| rs770134325 | in-del | -/AAAAATA | | | intron-variant | SNX9 | GRCh38.p7 | 6:157820282 | AACCCTGTCTCTACT[-/AAAAATA]AAAAATAAAAAATAA | 51429 |
| rs770139746 | snp | G/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157776374 | GACAACAGCCACAGA[G/T]AAATGACACGTTCTC | 51429 |
| rs770150557 | snp | A/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157895833 | CCAGAATGGAGTTCC[A/T]TGTGCTAGATGCTCC | 51429 |
| rs770152473 | snp | A/C | | | intron-variant | SNX9 | GRCh38.p7 | 6:157883787 | CAAATACCATGTCTT[A/C]TATAAAACCTTTTGT | 51429 |
| rs770161096 | snp | A/C | | | intron-variant | SNX9, LOC105378078 | GRCh38.p7 | 6:157889933 | ATTATGTCATTTAAT[A/C]CTTACAGGAGGATAA | 51429 |
| rs770163510 | snp | A/G | | | intron-variant | SNX9 | GRCh38.p7 | 6:157912304 | GCCTATTTCAGGCTT[A/G]TAAGAAATTCTCATA | 51429 |
| rs770182480 | snp | C/T | | | intron-variant | SNX9 | GRCh38.p7 | 6:157797859 | AATAAAATAGGAATC[C/T]GGAAGTCTATACTGA | 51429 |