| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs7769 | snp | A/G | 0.236724 | 0.249647 | intron-variant, utr-variant-3-prime, downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4360546 | TTCACTGGACCACAG[A/G]GGGAGGGGAATGTGA | 84954 |
| rs15093 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4360524 | GCAGAGCCTGGGGTC[A/C/T]GGAGGCTTCACTGGA | 84954 |
| rs1802365 | snp | G/T | | | intron-variant | MPND | GRCh38.p7 | 19:4349047 | CCACTATCCAGAACC[G/T]CCAATCTTTCGACCC | 84954 |
| rs2041772 | snp | A/G | 0.484561 | 0.0864931 | intron-variant | MPND | GRCh38.p7 | 19:4355038 | TGGGTATCCAGGGCC[A/G]GGTGGGCGGGGGCGT | 84954 |
| rs2041773 | snp | A/G | 0.487306 | 0.0786506 | intron-variant | MPND | GRCh38.p7 | 19:4355057 | GGGCGGGGGCGTTGG[A/G]GGACCGGGGTCACGG | 84954 |
| rs2041774 | snp | A/G | 0.485363 | 0.084286 | intron-variant | MPND | GRCh38.p7 | 19:4355206 | AGGTGGCATTCTGGG[A/G]AGGGTTGGGAAGGGA | 84954 |
| rs2041775 | snp | C/T | 0.428333 | 0.175206 | intron-variant | MPND | GRCh38.p7 | 19:4355303 | TGCCCGTCTGTGTGC[C/T]TGGGACCCCATGGTG | 84954 |
| rs2386601 | snp | C/T | 0.483199 | 0.0901004 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4341902 | GGTGATGTGCATCTG[C/T]AGTCCCAGCTAATTG | 84954 |
| rs3048292 | in-del | -/TTT | 0 | 0 | intron-variant | MPND | GRCh38.p7 | 19:4355353 | ttttttttttttttt[-/TTT]gagacggagtctcgc | 84954 |
| rs3810367 | snp | A/C | 0.482979 | 0.0906686 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342850 | TAGAAACCCTTAGTT[A/C]TGAGCGCAAACCATC | 84954 |
| rs3810368 | snp | C/T | 0.415563 | 0.18732 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342733 | AGGCAGGGCCGGGCT[C/T]GTTGCGCGCCTGATC | 84954 |
| rs4003316 | in-del | -/TT | | | intron-variant | MPND | GRCh38.p7 | 19:4348277 | ttttttttttttttt[-/TT]ngagacggagtctcg | 84954 |
| rs4435381 | snp | C/G | 0.464096 | 0.129085 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342288 | GAAAGTGCGTAAGGA[C/G]TTGGGGAAATAAACT | 84954 |
| rs4806980 | snp | C/G | 0.487177 | 0.0790385 | intron-variant | MPND | GRCh38.p7 | 19:4347172 | tgtttttgctgttat[C/G]gccttcaactgattg | 84954 |
| rs4806981 | snp | A/G | 0.435694 | 0.167385 | intron-variant | MPND | GRCh38.p7 | 19:4356285 | ATccaggcaccgggg[A/G]ttcacacctggaatc | 84954 |
| rs4807583 | snp | A/G | 0.0340491 | 0.125957 | synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357558 | CGAGTCCAAGATCTC[A/G]CCTTTCTGGGTGATG | 84954 |
| rs4807584 | snp | C/T | 0.483995 | 0.0880135 | intron-variant | MPND | GRCh38.p7 | 19:4357895 | AGGGCCCTGGCTCTC[C/T]TCTGGGCCTCTCCCA | 84954 |
| rs6510805 | snp | G/T | 0 | 0 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4343038 | AACGGTCCAATCATG[G/T]AATCAGTCGAGGGCC | 84954 |
| rs6510806 | snp | C/T | 0.306182 | 0.243605 | intron-variant | MPND | GRCh38.p7 | 19:4347271 | ttcaagacggagtct[C/T]gctctgtcgcccagg | 84954 |
| rs6510807 | snp | C/T | 0.459347 | 0.136653 | intron-variant | MPND | GRCh38.p7 | 19:4347576 | ACTTTTTTTTATGTA[C/T]GAAGTTTATTGCATG | 84954 |
| rs7245412 | snp | A/G | 0.499954 | 0.00479211 | intron-variant | MPND | GRCh38.p7 | 19:4345099 | gttgcccaggctgga[A/G]tgcagtagcatgatc | 84954 |
| rs7246177 | snp | C/T | 0.453087 | 0.145793 | intron-variant | MPND | GRCh38.p7 | 19:4353844 | AAAAAATTTCTTCTT[C/T]GTAAATAagagtctc | 84954 |
| rs7247827 | snp | C/T | 0.408188 | 0.193589 | intron-variant | MPND | GRCh38.p7 | 19:4350314 | caggtcatgcagggc[C/T]ctgtaggttatgggg | 84954 |
| rs7258168 | snp | A/G | 0.316 | 0.241131 | intron-variant | MPND | GRCh38.p7 | 19:4350200 | ccctggggcacgacc[A/G]tgcctggtgtgttgg | 84954 |
| rs8102860 | snp | A/G | 0.499203 | 0.0199521 | intron-variant | MPND | GRCh38.p7 | 19:4346351 | AACTTCAAATGCTAT[A/G]ATAATAGATGTTCCC | 84954 |
| rs8108076 | snp | C/T | 0.487871 | 0.076925 | intron-variant | MPND | GRCh38.p7 | 19:4347556 | CTGTAGATATGTTTT[C/T]ATAAACTTTTTTTTA | 84954 |
| rs8110781 | snp | G/T | 0.0463947 | 0.145069 | downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4360292 | GGGACCTCCTGGGGT[G/T]TGTGTGGCTTTGGAG | 84954 |
| rs8112334 | snp | C/T | 0.484209 | 0.0874434 | intron-variant | MPND | GRCh38.p7 | 19:4356764 | ctgcctcagcctcca[C/T]agtagatgggagtac | 84954 |
| rs8113766 | snp | G/T | 0 | 0 | intron-variant | MPND | GRCh38.p7 | 19:4344800 | ctggaatgcagttgc[G/T]cgatctcggctcact | 84954 |
| rs10401996 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4345165 | aattctcctgcctta[A/G]cctcttgagtagctg | 84954 |
| rs10406751 | snp | A/G | 0.467686 | 0.122935 | intron-variant | MPND | GRCh38.p7 | 19:4354609 | CAGTGGCTCACACCT[A/G]TAATCCCAGCACTTT | 84954 |
| rs10407203 | snp | A/G | 0.450985 | 0.148678 | intron-variant | MPND | GRCh38.p7 | 19:4354813 | AGGTTGCGGTGAGCC[A/G]AGATCGTGCCACTGC | 84954 |
| rs10407866 | snp | C/T | 0.413914 | 0.188765 | intron-variant | MPND | GRCh38.p7 | 19:4350175 | ttctgagaaacagcc[C/T]ctgcaaaggccctgg | 84954 |
| rs10411091 | snp | G/T | | | intron-variant | MPND | GRCh38.p7 | 19:4346873 | cgtctctactaaaaa[G/T]acaaaaattagccag | 84954 |
| rs10411614 | snp | A/G | 0.454784 | 0.1434 | intron-variant | MPND | GRCh38.p7 | 19:4355511 | CAGCTAATTTTTTGT[A/G]TTTTTAGTAGAGACG | 84954 |
| rs10412506 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | MPND | GRCh38.p7 | 19:4355915 | gatggagtgcagggc[A/G]cgatcttggctcact | 84954 |
| rs10412616 | snp | C/T | 0.454423 | 0.143914 | intron-variant | MPND | GRCh38.p7 | 19:4354705 | CCTGTCTCTACTAAA[C/T]ATACAAAAATTAGCT | 84954 |
| rs10412629 | snp | C/T | 0.00475057 | 0.0485048 | intron-variant | MPND | GRCh38.p7 | 19:4346857 | caacatggtgaaacc[C/T]cgtctctactaaaaa | 84954 |
| rs10414802 | snp | A/G | 0.01739 | 0.091611 | synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4343730 | GCCGCTGTCCCCGGC[A/G]GGCGGTGCGGGCGAG | 84954 |
| rs10420217 | snp | C/T | 0.48995 | 0.0701706 | intron-variant | MPND | GRCh38.p7 | 19:4355874 | tttttttttttttct[C/T]gagacattctcgctc | 84954 |
| rs10668030 | in-del | -/T | 0.5 | 0 | intron-variant | MPND | GRCh38.p7 | 19:4347909 | TTGTTTTTTTTTTTT[-/T]GAGACAGACTCTCGC | 84954 |
| rs11085070 | snp | A/G | 0.211212 | 0.246973 | intron-variant | MPND | GRCh38.p7 | 19:4353177 | TAAGTCTGGAGCCGG[A/G]CGAGGCCTGGGCTGA | 84954 |
| rs11085071 | snp | C/T | 0.484066 | 0.0878235 | intron-variant | MPND | GRCh38.p7 | 19:4353222 | CCCAGTTTTACTCAC[C/T]GCCTTGACTTCTTAA | 84954 |
| rs11453629 | in-del | -/T | 0 | 0 | intron-variant | MPND | GRCh38.p7 | 19:4356637 | TTCTTTTTTTTTTTT[-/T]CCTTTTCTTTGAGAC | 84954 |
| rs11666770 | snp | C/G | 0.335788 | 0.23482 | intron-variant | MPND | GRCh38.p7 | 19:4351655 | atcacaaggtcagac[C/G]atcgagaccatcctg | 84954 |
| rs11666771 | snp | A/G | 0.335788 | 0.23482 | intron-variant | MPND | GRCh38.p7 | 19:4351659 | caaggtcagacgatc[A/G]agaccatcctggcta | 84954 |
| rs11668153 | snp | C/T | 0.455621 | 0.142197 | intron-variant | MPND | GRCh38.p7 | 19:4352766 | TTCTCTGCTCCCTCC[C/T]TCCCTCTAGTGGTCA | 84954 |
| rs11668187 | snp | C/G | 0.389501 | 0.256676 | intron-variant | MPND | GRCh38.p7 | 19:4352841 | GGATTTAGCAGGGAG[C/G]GGGGGGGCACCCAGC | 84954 |
| rs11669297 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4348445 | tttgtatttttagta[A/G]aaatggggtttcacc | 84954 |
| rs11670483 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4349541 | ttgagatggagtgtc[A/G]ctcttgttgcccagg | 84954 |
| rs11670560 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | MPND | GRCh38.p7 | 19:4349098 | tttgagatggagtct[C/T]gctctgttgtccagg | 84954 |
| rs11881539 | snp | C/G | 0.441158 | 0.161117 | intron-variant | MPND | GRCh38.p7 | 19:4349659 | gggactacagatgcc[C/G]actaccatgcccagt | 84954 |
| rs11882587 | snp | A/G | 0.485817 | 0.083007 | synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4352962 | GGAGGACGTTCTGGC[A/G]GGGGTCTCAGCAGAG | 84954 |
| rs12462529 | snp | A/G | 0.318174 | 0.240525 | intron-variant | MPND | GRCh38.p7 | 19:4359528 | CCCAGGGTCCTGGCC[A/G]CCCCTGAGTGTCTTA | 84954 |
| rs12609239 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | MPND | GRCh38.p7 | 19:4352397 | TGTATTATAAAATGC[A/G]AGGTGagccgggtgc | 84954 |
| rs12985281 | snp | G/T | | | intron-variant | MPND | GRCh38.p7 | 19:4350223 | tgtgttggaggaaca[G/T]cgaggagcctgtgtg | 84954 |
| rs12985506 | snp | G/T | | | intron-variant | MPND | GRCh38.p7 | 19:4350310 | agggcaggtcatgca[G/T]ggctctgtaggttat | 84954 |
| rs16992360 | snp | C/G | 0.130008 | 0.219321 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342332 | GCTATGCTGAGTCTG[C/G]AGGCCTTGGGGATGC | 84954 |
| rs17853075 | snp | A/G | 0.000360642 | 0.0134235 | synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4343877 | CGGCGGCGGGGCCGG[A/G]GCGGGGGGCTGCGGC | 84954 |
| rs28725202 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | MPND | GRCh38.p7 | 19:4344522 | GGACGTAGATTACCA[A/G]ACACCCCATCCCACA | 84954 |
| rs28736724 | snp | C/T | 0.200801 | 0.245111 | intron-variant | MPND | GRCh38.p7 | 19:4344622 | CTGTGGTTTCCCAGC[C/T]GTGAAATGGAATATT | 84954 |
| rs34192297 | in-del | -/T | | | downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4360120 | GGGGTGAGGGTGGCT[-/T]GGGTGCCCAGGCTGG | 84954 |
| rs34505344 | in-del | -/A | | | intron-variant | MPND | GRCh38.p7 | 19:4347262 | TTTTTTTTTTCAAGA[-/A]CGGAGTCTTGCTCTG | 84954 |
| rs34522164 | snp | A/G | 0.0603079 | 0.16284 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4359194 | AGCCTCACGAGGTCA[A/G]GGGAACCCTTGTAGA | 84954 |
| rs34875067 | in-del | -/A | | | intron-variant | MPND | GRCh38.p7 | 19:4345143 | CCTCTGCCTCCCGGT[-/A]TCAAGCAATTCTCCT | 84954 |
| rs34883765 | in-del | -/G | | | intron-variant | MPND | GRCh38.p7 | 19:4358790 | GACCCTACCTCAAGG[-/G]AAAAAACCCAACAAA | 84954 |
| rs35121116 | in-del | -/C | | | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342464 | CCTGAGAACATTCCC[-/C]GAGCACCCTGGAGAG | 84954 |
| rs35289519 | in-del | -/C | | | intron-variant | MPND | GRCh38.p7 | 19:4359316 | GGCCCCCTGGGCAGC[-/C]TAAAAGGTGGCAGCA | 84954 |
| rs35324876 | in-del | -/T | | | intron-variant | MPND | GRCh38.p7 | 19:4348278 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCGC | 84954 |
| rs35351631 | in-del | -/T | | | intron-variant | MPND | GRCh38.p7 | 19:4354531 | GGCCTTGTCTGCTTT[-/T]GTTTGCTACTGGTAC | 84954 |
| rs35424646 | snp | A/G | 0.109461 | 0.206758 | intron-variant | MPND | GRCh38.p7 | 19:4353531 | CCTCGGCCTCCCAAA[A/G]TGTTGGGATTACAGG | 84954 |
| rs35431326 | in-del | -/T | | | intron-variant | MPND | GRCh38.p7 | 19:4349401 | GCCTTGGTGGGAACT[-/T]GCCTGTGGAAAGCAG | 84954 |
| rs35432330 | in-del | -/G | | | intron-variant | MPND | GRCh38.p7 | 19:4352849 | CAGGGAGAGGGGGGG[-/G]CACCCAGCTGAGGGT | 84954 |
| rs36091183 | in-del | -/T | | | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342495 | CTCCCCCGCACCCCT[-/T]ACTGTCCAGTTCCCA | 84954 |
| rs45561032 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | MPND | GRCh38.p7 | 19:4358169 | TGACATCCTTCACGA[A/G]ATGGTGAGCTCGCTG | 84954 |
| rs56331661 | in-del | -/TT | 0 | 0 | intron-variant | MPND | GRCh38.p7 | 19:4355870 | GCCTTTTTTTTTTTT[-/TT]CTTGAGACATTCTCG | 84954 |
| rs56332006 | snp | C/T | 0.0452528 | 0.143452 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4343293 | CGCCCCAGGCTTCCA[C/T]CTTGCAACCTCTATC | 84954 |
| rs56812200 | snp | A/G | 0.224709 | 0.248717 | intron-variant | MPND | GRCh38.p7 | 19:4350118 | AGGTGACATTTGAAC[A/G]GAGAACTGAAGGTGG | 84954 |
| rs56828298 | snp | A/C | 0.453697 | 0.14494 | intron-variant | MPND | GRCh38.p7 | 19:4352376 | CACCAAAGGTTGCGC[A/C]GGGCTTGTATTATAA | 84954 |
| rs56942202 | snp | A/C | 0.0622301 | 0.165053 | intron-variant | MPND | GRCh38.p7 | 19:4355458 | CTCCTGCCTCAGCCT[A/C]CTGAATAGCTGGGAC | 84954 |
| rs57747211 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4348287 | TTTTTTTGAGACGGA[A/G]TCTCGCTCTGTCGCC | 84954 |
| rs57770089 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4348281 | TTTTTTTTTTTTTGA[A/G]ACGGAGTCTCGCTCT | 84954 |
| rs58479594 | in-del | -/AA | | | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342053 | AAAAAAAAAAAAAAA[-/AA]GAAAAAAGAAAAGAA | 84954 |
| rs59062816 | snp | C/T | 0.031825 | 0.122064 | intron-variant | MPND | GRCh38.p7 | 19:4346309 | GGGGGCTGGAAATGA[C/T]GGCAGGGACCAGAGG | 84954 |
| rs59677849 | snp | C/T | 0.495855 | 0.045338 | intron-variant | MPND | GRCh38.p7 | 19:4349603 | GCAACCTCCGCCTCT[C/T]GGGTTCAGGCGATTC | 84954 |
| rs60284417 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4348330 | CAGTGGCACAATCTA[A/G]GCTCACTGCAACCTC | 84954 |
| rs60305318 | in-del | -/A | 0.434976 | 0.168179 | intron-variant | MPND | GRCh38.p7 | 19:4352720 | AAATTACAAATAAAT[-/A]AAAAAAAATGTGAGG | 84954 |
| rs60406459 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4349059 | TGGAGGTTCTGGATA[A/G]TGGACAAAAGATATA | 84954 |
| rs60697121 | snp | C/G | 0.215747 | 0.247642 | intron-variant | MPND | GRCh38.p7 | 19:4349419 | CTGTGGAAAGCAGTG[C/G]TGGCGGGAGAAGGCG | 84954 |
| rs60930749 | snp | C/T | 0.299158 | 0.245119 | intron-variant | MPND | GRCh38.p7 | 19:4350444 | GGCTGCTGTGGGGAC[C/T]AGACTGTCGGGGGTT | 84954 |
| rs61167639 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4356324 | TAGGGAGGCCGAGGC[A/G]GGAGGTTTGCTGGAG | 84954 |
| rs61730128 | snp | A/G | 0.0395694 | 0.134978 | synonymous-codon, intron-variant, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357312 | GTACCACAGCCACCC[A/G]CACAGCCCGGCGCTG | 84954 |
| rs61730129 | snp | A/G | 0.00075242 | 0.0193815 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357349 | CTGCAGGACATCGAC[A/G]CACAGATGGACTACC | 84954 |
| rs61730130 | snp | A/C/G | 0.00326723 | 0.0402874 | intron-variant | MPND | GRCh38.p7 | 19:4357229 | CAGGCCCCTGTGCCC[A/C/G]CTGAGCTGCGCCTCT | 84954 |
| rs62129340 | snp | C/T | 0.197082 | 0.244335 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4343188 | TTTCTCCCCTGGTCC[C/T]AAAGGCCGAGGCCTC | 84954 |
| rs62129341 | snp | A/G | 0.097727 | 0.198275 | intron-variant | MPND | GRCh38.p7 | 19:4347304 | GGAGTACAGTGGCAC[A/G]ATCTCAGCTCACTGC | 84954 |
| rs62129342 | snp | A/G | 0.448963 | 0.151372 | intron-variant | MPND | GRCh38.p7 | 19:4352034 | AAAAATTAGCCAGGC[A/G]TGGTGGTGGGCAACT | 84954 |
| rs62129345 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | MPND | GRCh38.p7 | 19:4356751 | GTTCAACATCCTCCT[G/T]CCTCAGCCTCCATAG | 84954 |
| rs67576371 | in-del | -/G | | | intron-variant | MPND | GRCh38.p7 | 19:4352841 | GATTTAGCAGGGAGC[-/G]GGGGGGGCACCCAGC | 84954 |
| rs67782188 | snp | C/G | 0.465158 | 0.127307 | intron-variant | MPND | GRCh38.p7 | 19:4351575 | ACAGATAAGAATAGA[C/G]TTGGCGGCCGGGCAC | 84954 |
| rs71166988 | in-del | -/A | 0.470908 | 0.117046 | intron-variant | MPND | GRCh38.p7 | 19:4346717 | CATAAGAAAAAAAAA[-/A]CGGCCAGTGCAGTAG | 84954 |
| rs71166989 | in-del | -/CAAAAAAA | 0 | 0 | intron-variant | MPND | GRCh38.p7 | 19:4353573 | AGCAAAACCCTGTCT[-/CAAAAAAA]CAAAAAAACAGGTAC | 84954 |
| rs71886973 | in-del | -/TGTTTTTT | 0.482905 | 0.0908579 | intron-variant | MPND | GRCh38.p7 | 19:4353563 | GTGAGCCACTGTACC[-/TGTTTTTT]TGTTTTTTTGAGACA | 84954 |
| rs72986780 | snp | A/G | 0.416545 | 0.186448 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4341750 | GAAAATAGGCTGGGC[A/G]CAGTGGCTCACACCT | 84954 |
| rs72986787 | snp | A/C | 0.33303 | 0.235809 | intron-variant | MPND | GRCh38.p7 | 19:4350009 | GGCCTGTTTTAGGCA[A/C]TGAATATAAAGCAGA | 84954 |
| rs72986788 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | MPND | GRCh38.p7 | 19:4351532 | CCTGATGCCATCCCC[G/T]TGGAGTTGGAGGTCA | 84954 |
| rs73537221 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4341587 | AAAAATTAGCCAGGC[A/G]TGCTGGTCACGCCTG | 84954 |
| rs73537284 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4343167 | CATTGTTCCCCTGGA[C/T]CTGAGTTTCTCCCCT | 84954 |
| rs73537292 | snp | C/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4343243 | CAGGTCTCACCTTCT[C/G]CTCTCCTTGCAGCAG | 84954 |
| rs73537295 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | MPND | GRCh38.p7 | 19:4344167 | AACTGAGGCCCGGGG[C/T]TCCGTTGACTGCAGG | 84954 |
| rs73539212 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | MPND | GRCh38.p7 | 19:4349461 | TGGAGCGTCAGGAAG[C/T]GAGGGTGCTCAACGG | 84954 |
| rs73539222 | snp | A/G | 0.471958 | 0.115042 | intron-variant | MPND | GRCh38.p7 | 19:4351601 | GGCACGGTGGCTCAC[A/G]CCTTTAATCCCAGCA | 84954 |
| rs73919880 | snp | C/T | 0.0700422 | 0.173537 | intron-variant | MPND | GRCh38.p7 | 19:4350761 | GAGAGGCAGCTGGGC[C/T]CTGAGTCTGGAGCCG | 84954 |
| rs73919881 | snp | C/T | 0.0962929 | 0.197165 | intron-variant | MPND | GRCh38.p7 | 19:4350961 | GTGGGATCCGGGGGT[C/T]GTGTGAGGACCGTGT | 84954 |
| rs73919882 | snp | C/T | 0.0988009 | 0.199095 | intron-variant | MPND | GRCh38.p7 | 19:4350979 | GTGAGGACCGTGTCC[C/T]GGTAGGTAGGAGGCT | 84954 |
| rs73919885 | snp | C/T | 0.0166842 | 0.0897982 | intron-variant | MPND | GRCh38.p7 | 19:4353064 | GAGGCAGGACAGGGG[C/T]GGATACAGCTCGGGT | 84954 |
| rs73919894 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | MPND | GRCh38.p7 | 19:4357110 | CACTGGACTCAGTGG[C/T]GGTGGGGGCAGGGCC | 84954 |
| rs73919895 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | MPND | GRCh38.p7 | 19:4357161 | CCCCAGGCCTGATAC[A/G]CAGCAGGAATTCGTT | 84954 |
| rs73919896 | snp | C/G | 0.018705 | 0.0948821 | intron-variant | MPND | GRCh38.p7 | 19:4357487 | GCCGAGCCTCCCAGG[C/G]CCAACCCCTCTCCCT | 84954 |
| rs74172637 | snp | A/G | 0.5 | 0 | intron-variant | MPND | GRCh38.p7 | 19:4346859 | ACATGGTGAAACCTC[A/G]TCTCTACTAAAAAGA | 84954 |
| rs74318543 | snp | A/C | 0.0792508 | 0.182605 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342491 | AGAGCCTCCCCCGCA[A/C]CCCTACTGTCCAGTT | 84954 |
| rs74428242 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | MPND | GRCh38.p7 | 19:4345477 | GACACAGCAGTGATC[A/C]AGACAGACAGACCCT | 84954 |
| rs75341105 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | MPND | GRCh38.p7 | 19:4359402 | CTGGTCACCCCGTGG[C/G]CACCCCAGCAGGGTG | 84954 |
| rs75511514 | snp | A/G | 0.033725 | 0.1254 | intron-variant | MPND | GRCh38.p7 | 19:4354517 | CTCCATGAGAGCTGG[A/G]GCCTTGTCTGCTTTG | 84954 |
| rs75578316 | snp | G/T | 0.5 | 0 | intron-variant | MPND | GRCh38.p7 | 19:4348676 | TTCTTTTTTTTTTTT[G/T]AGATGGAGTCTCACT | 84954 |
| rs75619885 | snp | C/T | 0.5 | 0 | intron-variant | MPND | GRCh38.p7 | 19:4347256 | ATGTTTTTTTTTTTT[C/T]TCAAGACGGAGTCTT | 84954 |
| rs75746739 | snp | C/T | 0.0567745 | 0.158631 | intron-variant | MPND | GRCh38.p7 | 19:4354494 | GGCGGGGCTCCCCTG[C/T]GTATCAGCTCCATGA | 84954 |
| rs75938485 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | MPND | GRCh38.p7 | 19:4358889 | GCCACGTCAGGCCCG[C/T]GTGGTTCTGGAGAAC | 84954 |
| rs75980609 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | MPND | GRCh38.p7 | 19:4347764 | CCATGAACCTGCCCG[A/G]CGCAGTGGCAAAAAA | 84954 |
| rs76298857 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | MPND | GRCh38.p7 | 19:4359035 | AGGTCACTCGTGATC[G/T]CTTTGTGGTTGGTTT | 84954 |
| rs76467764 | snp | C/G | 0.0130921 | 0.0798413 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4343268 | CAGCAGGCTGAGCCA[C/G]TCGCGCACCCGCCCC | 84954 |
| rs77205429 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant, utr-variant-3-prime, downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4360429 | TACATTTCAGTTTGC[C/T]CTGGACCGTGCCCAA | 84954 |
| rs77610894 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | MPND | GRCh38.p7 | 19:4350875 | TGGGAGGGGTGTGGA[A/G]GGAGGAGGCCTGAAA | 84954 |
| rs77625417 | snp | C/T | 0.0836354 | 0.186609 | intron-variant | MPND | GRCh38.p7 | 19:4358309 | GGTTAGGGCTTCTTC[C/T]ATCACTCAGGACAGA | 84954 |
| rs77782994 | snp | A/G | 9.93197e-05 | 0.00704627 | intron-variant, downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4359909 | AGGCCCAGCCCCCTC[A/G]TTTCAGATCTCCTTG | 84954 |
| rs77944096 | snp | A/C | 0.0584853 | 0.160693 | intron-variant | MPND | GRCh38.p7 | 19:4359422 | CCAGCAGGGTGCAGG[A/C]CAGATTTGATTGGAC | 84954 |
| rs78046835 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | MPND | GRCh38.p7 | 19:4350532 | TGGAGTGGCCCAGGC[C/T]GACCATGGAGCAGGG | 84954 |
| rs78638995 | snp | C/G | 0.5 | 0 | intron-variant | MPND | GRCh38.p7 | 19:4350492 | CCAGGGCAGAGGTGA[C/G]TGAGCTGGTCCAGGT | 84954 |
| rs78702831 | in-del | -/GAA | 0.0926964 | 0.194308 | intron-variant | MPND | GRCh38.p7 | 19:4346797 | GCATTTTGGGAGGCT[-/GAA]GCAGGCAGGTTCACG | 84954 |
| rs78866247 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | MPND | GRCh38.p7 | 19:4346365 | TGATAATAGATGTTC[C/G]CTGAGTGTTCACCAG | 84954 |
| rs78892323 | snp | A/T | 0.5 | 0 | intron-variant | MPND | GRCh38.p7 | 19:4348661 | CATTTTTCTGTTGAA[A/T]TCTTTTTTTTTTTTG | 84954 |
| rs78984910 | snp | C/G | 0.0685596 | 0.171987 | intron-variant | MPND | GRCh38.p7 | 19:4359818 | GCCTCGGTCTCAGGG[C/G]GGCTCAGTCAGGATG | 84954 |
| rs79110543 | snp | C/T | 0.0696718 | 0.173152 | intron-variant | MPND | GRCh38.p7 | 19:4351025 | CTGCCGAGAAGGTGA[C/T]GAGGACAGAAAGTGA | 84954 |
| rs79127761 | in-del | -/A | 0.370974 | 0.218781 | intron-variant | MPND | GRCh38.p7 | 19:4350029 | TATAAAGCAGAGGGC[-/A]AAAAAAGTCAAAAAT | 84954 |
| rs79744248 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | MPND | GRCh38.p7 | 19:4352333 | GCGTTCCAATAATGG[A/G]ACCCTAGGCATAAAT | 84954 |
| rs79831308 | snp | A/G | 0.0137327 | 0.0817174 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4359202 | GGTTCCCCTGACCTC[A/G]TGAGGCTCCAGGAAC | 84954 |
| rs111365129 | snp | A/G | | | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4343473 | CACCCCAGCGCGCCG[A/G]GCCCTTCCCCCGACC | 84954 |
| rs111445219 | snp | G/T | 0.0146672 | 0.084371 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4343111 | CTTGGGCTCTTTGGC[G/T]CCACCTGTGTCTGCG | 84954 |
| rs111765325 | in-del | -/A | 0.0995161 | 0.199636 | intron-variant | MPND | GRCh38.p7 | 19:4352840 | GGATTTAGCAGGGAG[-/A]CGGGGGGGCACCCAG | 84954 |
| rs112213335 | snp | C/T | 0 | 0 | intron-variant | MPND | GRCh38.p7 | 19:4353897 | GCAGTGGTGTGATCA[C/T]AGCTCCCTGCAGCCT | 84954 |
| rs112642376 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MPND | GRCh38.p7 | 19:4353961 | AGCACTGGGATTATA[A/G]GCATGCACCACCACA | 84954 |
| rs112901068 | snp | A/C | | | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4343911 | CCCGGGGGCGCGCTC[A/C]CCAGGCGCGCGGTCA | 84954 |
| rs113072364 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | MPND | GRCh38.p7 | 19:4353931 | CCTCCCATGCTCAAG[C/T]GATCCTCCTGCTTCA | 84954 |
| rs113074078 | snp | C/T | 0.077417 | 0.180873 | intron-variant | MPND | GRCh38.p7 | 19:4347530 | AAGTGTGAGCCACCG[C/T]GCCCAGCTGCCTGTA | 84954 |
| rs113192466 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | MPND | GRCh38.p7 | 19:4344996 | GTCCGCCTGCCTCAG[C/T]TCCCAAAGTGCTGGG | 84954 |
| rs113195632 | snp | C/T | 0.5 | 0 | intron-variant | MPND | GRCh38.p7 | 19:4359556 | TTAGGGTAGTGGTTC[C/T]TGGTTTCCCTCCACC | 84954 |
| rs113205784 | snp | C/G | 0.000758497 | 0.0194595 | intron-variant | MPND | GRCh38.p7 | 19:4354924 | ACAGCCTGAGCCAGT[C/G]TTTTGCTGTTCCTCC | 84954 |
| rs113317103 | snp | C/G | | | intron-variant | MPND | GRCh38.p7 | 19:4345030 | ATAGGCGTGAGCCAC[C/G]ATGCCCGGCCTTTTT | 84954 |
| rs113430891 | snp | C/G | 0 | 0 | intron-variant | MPND | GRCh38.p7 | 19:4351205 | GCCTCCCGGGTTCAA[C/G]TGATCCTCCTGCCTC | 84954 |
| rs113448087 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MPND | GRCh38.p7 | 19:4353937 | ATGCTCAAGCGATCC[C/T]CCTGCTTCAGCACTG | 84954 |
| rs113741565 | snp | A/G | 0.444267 | 0.157354 | intron-variant | MPND | GRCh38.p7 | 19:4351944 | TTGGGAGGCTGAGGC[A/G]GGTGGGTCACTTGAG | 84954 |
| rs114040640 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | MPND | GRCh38.p7 | 19:4348208 | ACTTATCCATATTCT[A/G]GATGCTCAATTACAG | 84954 |
| rs114086165 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | MPND | GRCh38.p7 | 19:4352406 | AAATGCGAGGTGAGC[C/T]GGGTGCGGTGGCTTA | 84954 |
| rs114249371 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | MPND | GRCh38.p7 | 19:4350435 | TTCTCTGGTGGCTGC[C/T]GTGGGGACTAGACTG | 84954 |
| rs114389168 | snp | A/C | 0.02016 | 0.0983543 | intron-variant | MPND | GRCh38.p7 | 19:4347068 | AATGGAGATGGTACC[A/C]GTGCCCATGTGTGGA | 84954 |
| rs114708281 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | MPND | GRCh38.p7 | 19:4351135 | TGTAGACAGAGTCTC[A/G]CTCCGTCACCCAGGC | 84954 |
| rs114942344 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | MPND | GRCh38.p7 | 19:4347102 | TGTAGGGCAGGCAGG[A/T]AACTGAGGCAGGAGC | 84954 |
| rs115000984 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | MPND | GRCh38.p7 | 19:4345581 | GATCAGGTTTGTGGG[A/T]GTGGACTCCCAGGCA | 84954 |
| rs115079396 | snp | A/G | 0.00597247 | 0.0543191 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342256 | TGGAAGGCAGGGGAC[A/G]GAAAAAAAGCCAAAG | 84954 |
| rs115174877 | snp | A/G | | | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4343061 | CGAGGGCCGCCCGGG[A/G]GGGTGGGAGTTAATT | 84954 |
| rs115655617 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342947 | CGGATTGGTTGGTGC[A/G]GGAATCCAGTAGCTT | 84954 |
| rs115724127 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | MPND | GRCh38.p7 | 19:4349073 | AGTGGACAAAAGATA[C/T]AATTCTGTTTTTGAG | 84954 |
| rs115921561 | snp | C/T | 0.0205511 | 0.0992634 | downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4360172 | ACTTCCAGGGCAGGG[C/T]ATTAACTTCCAGGAT | 84954 |
| rs116041774 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | MPND | GRCh38.p7 | 19:4351026 | TGCCGAGAAGGTGAC[A/G]AGGACAGAAAGTGAG | 84954 |
| rs116132099 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4356375 | ACAGCAAGACCCCGT[C/G]TCTACAAAAGATAAA | 84954 |
| rs116344921 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | MPND | GRCh38.p7 | 19:4350975 | TTGTGTGAGGACCGT[C/G]TCCTGGTAGGTAGGA | 84954 |
| rs116423832 | snp | A/G | 0.0693013 | 0.172766 | intron-variant | MPND | GRCh38.p7 | 19:4350087 | GAAGAAGGTGGTTGG[A/G]GGGGCTTCACTGAGA | 84954 |
| rs116888401 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | MPND | GRCh38.p7 | 19:4351452 | CTATGTATGGTGCTG[C/G]CTCGCTCAATGAACG | 84954 |
| rs116912638 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MPND | GRCh38.p7 | 19:4358751 | GAGATCACGCCACTG[C/T]GCTCCAGTCTGGGCC | 84954 |
| rs117083085 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | MPND | GRCh38.p7 | 19:4346243 | GATGGAATGGCATAC[G/T]CAAAGTCATGTAGAC | 84954 |
| rs117613418 | snp | C/T | 0.00570852 | 0.0531194 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4354083 | GTGGACAGCAAGATC[C/T]GGGTTCCGGTCCGCT | 84954 |
| rs117686080 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4343063 | AGGGCCGCCCGGGAG[A/G]GTGGGAGTTAATTCT | 84954 |
| rs117689055 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | MPND | GRCh38.p7 | 19:4348970 | TCTGTTGAATTCTTA[C/T]ATGGATACAGTCCTC | 84954 |
| rs117699169 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | MPND | GRCh38.p7 | 19:4344840 | GCCTCCCGGTTCAAG[C/G]GATTTTCTGCCTCAG | 84954 |
| rs117904397 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | MPND | GRCh38.p7 | 19:4351631 | ACTTTGGGTGGCCGA[A/G]ATGGGCAAATCACAA | 84954 |
| rs118054049 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MPND | GRCh38.p7 | 19:4349410 | GGGAACTGCCTGTGG[A/G]AAGCAGTGGTGGCGG | 84954 |
| rs138256636 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | MPND | GRCh38.p7 | 19:4352191 | GAAAAAAAAAAAGAT[A/T]AAAGAATAGATAGAG | 84954 |
| rs138298638 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | MPND | GRCh38.p7 | 19:4356716 | CATAATCATGGCTCA[C/G]TGCAGCATCAGCTGC | 84954 |
| rs138358352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4346179 | CTTGGGCTTTGAGGG[A/G]TGAGCAGGAGTTTGT | 84954 |
| rs138412578 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | MPND | GRCh38.p7 | 19:4346845 | GACCAGCCTGGCCAA[C/G]ATGGTGAAACCCCGT | 84954 |
| rs138550974 | in-del | -/GGGGGGG | | | intron-variant | MPND | GRCh38.p7 | 19:4357110 | ACTGGACTCAGTGGC[-/GGGGGGG]GGTGGGGGCAGGGCC | 84954 |
| rs138716070 | in-del | -/T | 0.379354 | 0.213933 | intron-variant | MPND | GRCh38.p7 | 19:4347244 | CTTTTCGTAGATATG[-/T]TTTTTTTTTTTTTCA | 84954 |
| rs139367126 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | MPND | GRCh38.p7 | 19:4349498 | GCCGAGTCCTCAGTG[C/G]CTCAGTGAGTGGGTC | 84954 |
| rs139373887 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | MPND | GRCh38.p7 | 19:4348111 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACATCA | 84954 |
| rs139410726 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | MPND | GRCh38.p7 | 19:4350275 | GAGAGAGAAGGAGGT[A/G]GGGAGGATGGGAAGG | 84954 |
| rs139928086 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342858 | GCGCTCATAACTAAG[C/G/T]GTTTCTACTGATTGG | 84954 |
| rs139962989 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | MPND | GRCh38.p7 | 19:4344189 | GACTGCAGGAAGAGC[C/T]CCAGTGTGAGGAGGG | 84954 |
| rs139965365 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | MPND | GRCh38.p7 | 19:4352565 | GGTGCATGCCTGTAA[C/T]CCCAGCTACTCAGGA | 84954 |
| rs139993672 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4360315 | CTTTGGAGCCGGCCC[C/T]TCAGGAAGGCGGTGG | 84954 |
| rs140123477 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | MPND | GRCh38.p7 | 19:4349401 | TGCCTTGGTGGGAAC[G/T]GCCTGTGGAAAGCAG | 84954 |
| rs140159585 | in-del | -/TTC | 0.00199601 | 0.0315281 | intron-variant | MPND | GRCh38.p7 | 19:4349173 | CCCGGGTTCACGCAA[-/TTC]TTCTGCGTCAGCCTC | 84954 |
| rs140324479 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MPND | GRCh38.p7 | 19:4354640 | GGGAAGCTGAGGCAG[C/T]GGGTCACCTGAACTC | 84954 |
| rs140545342 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | MPND | GRCh38.p7 | 19:4356026 | CTCCAGCTAATTTTT[C/G]TATTTTTAGTTGAGA | 84954 |
| rs140872790 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | MPND | GRCh38.p7 | 19:4345682 | AGGTCTGGGGAGGAC[C/G]CCCCGGGAGAGAGGG | 84954 |
| rs140910489 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | MPND | GRCh38.p7 | 19:4348748 | CTGCAAACTCTGCCT[C/T]CCGGATTCAAGCCAT | 84954 |
| rs141061637 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | MPND | GRCh38.p7 | 19:4351828 | GATCATGCCACTGCA[C/T]TCCAGCCTCGGCGAC | 84954 |
| rs141422675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4350115 | AGAAGGTGACATTTG[A/G]ACGGAGAACTGAAGG | 84954 |
| rs141604138 | in-del | -/C | 0.0225045 | 0.103662 | intron-variant | MPND | GRCh38.p7 | 19:4349355 | TGCAGGGATTACAGG[-/C]ATGAGCCACCGCAGC | 84954 |
| rs141733787 | snp | C/T | 0.000166578 | 0.00912476 | synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4359201 | GGGTTCCCCTGACCT[C/T]GTGAGGCTCCAGGAA | 84954 |
| rs141830080 | snp | G/T | 0.0930568 | 0.194599 | intron-variant | MPND | GRCh38.p7 | 19:4349538 | TTTTTGAGATGGAGT[G/T]TCGCTCTTGTTGCCC | 84954 |
| rs142136634 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | MPND | GRCh38.p7 | 19:4348897 | CCTGACCTCGTGATC[C/T]ACCTGCCTCAGCCTC | 84954 |
| rs142592251 | in-del | -/GATTCAAGT | 0.0441095 | 0.141807 | intron-variant | MPND | GRCh38.p7 | 19:4355948 | AACCTCCACCTTCCG[-/GATTCAAGT]GATTCTCCTGCCTCT | 84954 |
| rs142763003 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | MPND | GRCh38.p7 | 19:4352336 | TTCCAATAATGGAAC[C/T]CTAGGCATAAATGGC | 84954 |
| rs142802033 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4357000 | TCTGTAAGCTGGGCT[A/G]CAGCAGTGAACAAAA | 84954 |
| rs143251197 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | MPND | GRCh38.p7 | 19:4346677 | CCACCTGGACTTCCC[A/G]AAGTGTTGGGATTGC | 84954 |
| rs143419408 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | MPND | GRCh38.p7 | 19:4346459 | GTCTCACTCTGTGGC[C/T]CAGGCTGGAGTGCAG | 84954 |
| rs143889371 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4347173 | GTTTTTGCTGTTATC[C/G]CCTTCAACTGATTGG | 84954 |
| rs143989176 | snp | A/C/T | 0.00835141 | 0.0640778 | intron-variant | MPND | GRCh38.p7 | 19:4349661 | GACTACAGATGCCCA[A/C/T]TACCATGCCCAGTTA | 84954 |
| rs144107502 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | MPND | GRCh38.p7 | 19:4348144 | TGATCCGCCCGCCTC[C/T]GCCTCCCAAAATGCT | 84954 |
| rs144127552 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | MPND | GRCh38.p7 | 19:4350573 | CAGGTTCCAGGTATT[G/T]TTGGAAGTGTATCCG | 84954 |
| rs144153994 | in-del | -/GTGCTG | 0.0441095 | 0.141807 | intron-variant | MPND | GRCh38.p7 | 19:4355987 | CCTCCTGAATACCTA[-/GTGCTG]GGATTACAGGTGTGC | 84954 |
| rs144224824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4359406 | TCACCCCGTGGCCAC[C/T]CCAGCAGGGTGCAGG | 84954 |
| rs144299892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4349741 | GTCTTGAACTCCTGA[C/T]CTCAGGTGATCCGCC | 84954 |
| rs144575905 | snp | C/T | 0.0119091 | 0.0762411 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4341706 | CTCCAGCCTGGGAGA[C/T]AGAGCAAGGCCCTGT | 84954 |
| rs144604946 | snp | A/C/G | 5.02848e-05 | 0.00501401 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4345878 | CCAAGAAGTCGGGCT[A/C/G]TGGCTGGGCCTCTGT | 84954 |
| rs144642882 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | MPND | GRCh38.p7 | 19:4347586 | ATGTACGAAGTTTAT[C/T]GCATGAAGGAGTTAA | 84954 |
| rs144955789 | snp | C/T | 0.00054269 | 0.0164636 | intron-variant | MPND | GRCh38.p7 | 19:4357228 | TCAGGCCCCTGTGCC[C/T]GCTGAGCTGCGCCTC | 84954 |
| rs145167612 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | MPND | GRCh38.p7 | 19:4344424 | TCCCGTGGAGGGGAC[A/C]CTGAGGCCCGGAGCT | 84954 |
| rs145362378 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | MPND | GRCh38.p7 | 19:4344264 | CATGAAGAGGGGAGA[C/T]TGAGGCCCGGAGCTC | 84954 |
| rs145532743 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4351148 | TCGCTCCGTCACCCA[C/G]GCTGTAGTACAATGG | 84954 |
| rs145738083 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | MPND | GRCh38.p7 | 19:4356400 | GATAAAAAAAATTAG[C/T]CAGACATGGTGGTAC | 84954 |
| rs145835638 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4347425 | TTTGTATTTTTAGTA[A/G]AGACGGGGTTTCACC | 84954 |
| rs145863417 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, utr-variant-3-prime, downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4360533 | GGGGTCCGGAGGCTT[C/T]ACTGGACCACAGGGG | 84954 |
| rs146027033 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MPND | GRCh38.p7 | 19:4350954 | GGCGAGCGTGGGATC[C/T]GGGGGTTGTGTGAGG | 84954 |
| rs146039402 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | MPND | GRCh38.p7 | 19:4352420 | CCGGGTGCGGTGGCT[C/T]ACGCCTGTAATCCCA | 84954 |
| rs146457914 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | MPND | GRCh38.p7 | 19:4345364 | GTATTATTACTATTA[C/T]TGTTGTCATTATTGT | 84954 |
| rs146471134 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | MPND | GRCh38.p7 | 19:4348494 | TCAAACTCCTGACCT[C/T]GTGATCCACCCCCAT | 84954 |
| rs147089061 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | MPND | GRCh38.p7 | 19:4349571 | GCTGGAGCGCAATGG[C/T]GTGATCTTGGCTCAC | 84954 |
| rs147124916 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | MPND | GRCh38.p7 | 19:4351666 | AGACGATCGAGACCA[G/T]CCTGGCTAACACGGT | 84954 |
| rs147339989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4359638 | GTGGTGTCCCCATGG[A/G]TGTCTGGAACCAGGC | 84954 |
| rs147550021 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4351647 | ATGGGCAAATCACAA[A/G]GTCAGACGATCGAGA | 84954 |
| rs147586556 | snp | C/T | 0.0576578 | 0.159701 | intron-variant | MPND | GRCh38.p7 | 19:4354551 | GCTACTGGTACACTG[C/T]GGGTGCTCAATAAAT | 84954 |
| rs147739356 | snp | A/G | 0.0955749 | 0.196603 | intron-variant | MPND | GRCh38.p7 | 19:4351674 | GAGACCATCCTGGCT[A/G]ACACGGTGAAACCCC | 84954 |
| rs147980399 | in-del | -/AAC | 0.0023933 | 0.0345097 | intron-variant | MPND | GRCh38.p7 | 19:4347031 | GAGACTCCATTTCAA[-/AAC]AACAACAACAAAACC | 84954 |
| rs148172040 | snp | A/G | 0.0966517 | 0.197444 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4341725 | GCAAGGCCCTGTCTC[A/G]AAAAGAAAAGAAAAT | 84954 |
| rs148320883 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4350089 | AGAAGGTGGTTGGGG[A/G]GGCTTCACTGAGAAG | 84954 |
| rs148371531 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | MPND | GRCh38.p7 | 19:4346542 | CCCACCTCAGCCTCC[C/T]TAGTAGCTGGACTAC | 84954 |
| rs148420823 | snp | C/G | 0.0329836 | 0.124112 | intron-variant | MPND | GRCh38.p7 | 19:4351258 | GCAGGTGTTCGCCAC[C/G]ATGCCTGGCTAATTT | 84954 |
| rs148691632 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | MPND | GRCh38.p7 | 19:4344430 | GGAGGGGACACTGAG[G/T]CCCGGAGCTCTTTTT | 84954 |
| rs148822104 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4346399 | GGTGAACTTGACCAA[A/G]GACCCTTTGTGTGCC | 84954 |
| rs149210749 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MPND | GRCh38.p7 | 19:4355399 | AGAGTGCAGTGGTGC[A/G]ATCTCAGCTCCCTGC | 84954 |
| rs149311801 | snp | C/T | 0.00188738 | 0.0306615 | intron-variant, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357961 | ACCAGGTGCCGATCC[C/T]GGTGCAGAGCTGAGC | 84954 |
| rs149363974 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | MPND | GRCh38.p7 | 19:4352081 | AGGAGGCTGAGGCAA[A/G]AGAATGGCTTGAACC | 84954 |
| rs149861857 | snp | A/G | 0.00398564 | 0.0444627 | downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4360331 | TCAGGAAGGCGGTGG[A/G]TGGCAGGCCCACCCC | 84954 |
| rs150670124 | snp | A/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342257 | GGAAGGCAGGGGACG[A/G/T]AAAAAAAGCCAAAGA | 84954 |
| rs150816512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4350137 | AACTGAAGGTGGGGA[A/G]GGAGGGAGGGTGCCA | 84954 |
| rs180703564 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4356201 | GCTGAAACCTCGCCA[C/G]CCCCCTCCCCTCTCA | 84954 |
| rs180928318 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4352097 | AGAATGGCTTGAACC[C/T]GGAAGGCAGAGGTTG | 84954 |
| rs181118012 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4355545 | TTTCACCGCGTTAGC[C/T]AGGATGGTCTCGATC | 84954 |
| rs181192141 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | MPND | GRCh38.p7 | 19:4347580 | TTTTTTATGTACGAA[A/G]TTTATTGCATGAAGG | 84954 |
| rs181348862 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | MPND | GRCh38.p7 | 19:4351723 | AAAAATTAGCTGGGC[A/G]TGGTGGCACATGCCT | 84954 |
| rs181458696 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4360346 | GTGGCAGGCCCACCC[C/T]TGCACCAAGACGAGG | 84954 |
| rs181472473 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342859 | CGCTCATAACTAAGG[C/G]TTTCTACTGATTGGT | 84954 |
| rs181661094 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MPND | GRCh38.p7 | 19:4351589 | ACTTGGCGGCCGGGC[A/G]CGGTGGCTCACGCCT | 84954 |
| rs182087326 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | MPND | GRCh38.p7 | 19:4347155 | AATCTTTTTTTTTTT[C/T]CTGTTTTTGCTGTTA | 84954 |
| rs182288804 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4358863 | TGCTGGGGATGAGGC[C/T]GAACCAGGGGGCCAC | 84954 |
| rs182308842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4356417 | AGACATGGTGGTACG[C/T]ACCTGTAGTCCCATC | 84954 |
| rs182642497 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4345115 | TGCAGTAGCATGATC[G/T]CGGCTCACTGCAACC | 84954 |
| rs182643246 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | MPND | GRCh38.p7 | 19:4348015 | TCCTGCCTCAGTCTC[C/G]CGAGTAGCTGGGATT | 84954 |
| rs182718399 | snp | C/T | 6.43853e-05 | 0.00567349 | intron-variant | MPND | GRCh38.p7 | 19:4346019 | GGAAGCCGCCCAGGT[C/T]ACTGTGGAATGAGGG | 84954 |
| rs182793142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4353454 | TGTATTTTTAGTAGA[A/G]ATGGAGTTTCACAAT | 84954 |
| rs183101503 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MPND | GRCh38.p7 | 19:4356617 | TATTAAACACTACTC[A/G]TAAGTGCCAGTTGCT | 84954 |
| rs183409913 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | MPND | GRCh38.p7 | 19:4348291 | TTTGAGACGGAGTCT[C/T]GCTCTGTCGCCCAGG | 84954 |
| rs183497878 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4348972 | TGTTGAATTCTTATA[A/T]GGATACAGTCCTCAG | 84954 |
| rs183773208 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4349722 | CACCATGTTGGCCAG[C/G]CTAGTCTTGAACTCC | 84954 |
| rs183837761 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | MPND | GRCh38.p7 | 19:4346940 | GAGGCTGAGGCAGGA[A/G]AATCACTTGAACCTG | 84954 |
| rs183840530 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | MPND | GRCh38.p7 | 19:4353950 | CCTCCTGCTTCAGCA[C/G]TGGGATTATAGGCAT | 84954 |
| rs183882782 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | MPND | GRCh38.p7 | 19:4355587 | TGATCTGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 84954 |
| rs184012712 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MPND | GRCh38.p7 | 19:4357795 | ATTGGCTGCTCAGTA[C/T]AAAGAGGGCTCCCTT | 84954 |
| rs184369689 | snp | A/G | 9.58359e-05 | 0.00692162 | intron-variant | MPND | GRCh38.p7 | 19:4358196 | GCTGCGGGGCGGGCA[A/G]GCAGGGGCTGGCAGT | 84954 |
| rs184445352 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | MPND | GRCh38.p7 | 19:4358620 | TGGCGAAACCCTGTC[A/T]CTACCAAGATAGAAA | 84954 |
| rs184999055 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | MPND | GRCh38.p7 | 19:4346441 | CTTTTTTTTTGAGAC[A/G]GGGTCTCACTCTGTG | 84954 |
| rs185013824 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4351580 | TAAGAATAGACTTGG[C/G/T]GGCCGGGCACGGTGG | 84954 |
| rs185024715 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | MPND | GRCh38.p7 | 19:4351900 | AGAGTTGGCTGGGCA[C/T]GGTGGCTCACACCTG | 84954 |
| rs185086494 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4348052 | GCCCACCACCACACC[C/T]GGCTAATTTTTATAT | 84954 |
| rs185206915 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4351720 | ACAAAAAATTAGCTG[G/T]GCGTGGTGGCACATG | 84954 |
| rs185268743 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MPND | GRCh38.p7 | 19:4355421 | GCTCCCTGCAAGCTC[C/T]GCCTCCCGGGTTCAC | 84954 |
| rs185557449 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MPND | GRCh38.p7 | 19:4356920 | ACTGGGATTATAGGC[A/G]TGAGCCACTGCTCCC | 84954 |
| rs185888785 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | MPND | GRCh38.p7 | 19:4344775 | ACAGAGTCTCGCTTT[G/T]TTGCCCAGGCTGGAA | 84954 |
| rs185978829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4356278 | CCATCAGATCCAGGC[A/G]CCGGGGGTTCACACC | 84954 |
| rs186050982 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4347200 | TTGGATGAGGCCCAC[C/G]TGTAGTATCAAGAGT | 84954 |
| rs186106254 | snp | C/T | 0.00517822 | 0.0506191 | downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4360357 | ACCCCTGCACCAAGA[C/T]GAGGCAAGGGGCTGT | 84954 |
| rs186110586 | snp | A/C | 0.00279162 | 0.0372561 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4343266 | TGCAGCAGGCTGAGC[A/C]ACTCGCGCACCCGCC | 84954 |
| rs186346970 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342514 | GTCCAGTTCCCACTT[C/T]CCGACTGCGGTCTGG | 84954 |
| rs186388234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4347955 | GGAATGCAATGCCAC[A/G]ATCTCTGCTCATTGC | 84954 |
| rs186688678 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | MPND | GRCh38.p7 | 19:4353548 | GTTGGGATTACAGGC[C/G]TGAGCCACTGTACCT | 84954 |
| rs186894373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4356440 | GTCCCATCTATTTGA[A/G]AGGCTGAGGCAGGAG | 84954 |
| rs186942586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4351382 | TGCTGGGATTGCAGG[C/T]GTGGGCCACTGTGCC | 84954 |
| rs187064868 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MPND | GRCh38.p7 | 19:4359330 | CCTAAAAGGTGGCAG[C/T]AATGAGCCCCGTGGG | 84954 |
| rs187243966 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MPND | GRCh38.p7 | 19:4352566 | GTGCATGCCTGTAAC[C/T]CCAGCTACTCAGGAG | 84954 |
| rs187297461 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | MPND | GRCh38.p7 | 19:4348292 | TTGAGACGGAGTCTC[C/G]CTCTGTCGCCCAGGC | 84954 |
| rs187516797 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4346108 | ATGGAGCCCTTACCA[A/C]GTGACATGCCTCCTC | 84954 |
| rs187586077 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | MPND | GRCh38.p7 | 19:4345156 | GGTTCAAGCAATTCT[C/T]CTGCCTTAGCCTCTT | 84954 |
| rs187767445 | snp | A/C/T | 0.000391037 | 0.0139778 | intron-variant | MPND | GRCh38.p7 | 19:4357509 | CCTCTCCCTCTCTCC[A/C/T]GCCAGCCCCTTACTA | 84954 |
| rs188111170 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4349154 | CTCACTGCAACCTCC[C/T]GTTCCCGGGTTCACG | 84954 |
| rs188373339 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | MPND | GRCh38.p7 | 19:4358383 | ACCTCCCCACCTGCT[C/G]TTCTCTAAGGCACTG | 84954 |
| rs188571866 | snp | A/C/G | 0.00172499 | 0.0293192 | intron-variant | MPND | GRCh38.p7 | 19:4353065 | AGGCAGGACAGGGGC[A/C/G]GATACAGCTCGGGTT | 84954 |
| rs188891878 | snp | A/G | 1.70217e-05 | 0.00291729 | intron-variant | MPND | GRCh38.p7 | 19:4354016 | AACTTGGGCTGGGGA[A/G]GGACTGACCCTGCCT | 84954 |
| rs189146767 | snp | A/G | 0.00140154 | 0.0264349 | intron-variant, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357995 | GGTGTGCACTCTCCC[A/G]TTCCCAGCCCGGGCA | 84954 |
| rs189290854 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4346962 | TTGAACCTGCAAGGC[A/G]GAGGTTGCAGTGAGC | 84954 |
| rs189318396 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4358769 | TCCAGTCTGGGCCAC[A/G]GAGTGAGACCCTACC | 84954 |
| rs189518105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4359503 | TTGGGAGTGGCTCCC[C/T]TGCAGAGGGCCCAGG | 84954 |
| rs189528675 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342608 | GGACTTTCAACCCTG[C/T]CAGGGACTGAGGGAA | 84954 |
| rs189663465 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MPND | GRCh38.p7 | 19:4351722 | AAAAAATTAGCTGGG[C/T]GTGGTGGCACATGCC | 84954 |
| rs189671004 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4346524 | CTGGGTTCAAGCGAT[A/C]CTCCCACCTCAGCCT | 84954 |
| rs189828212 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | MPND | GRCh38.p7 | 19:4351943 | TTTGGGAGGCTGAGG[C/T]AGGTGGGTCACTTGA | 84954 |
| rs190144517 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MPND | GRCh38.p7 | 19:4355537 | AGACGGGGTTTCACC[A/G]CGTTAGCCAGGATGG | 84954 |
| rs190280384 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | MPND | GRCh38.p7 | 19:4357005 | AAGCTGGGCTACAGC[A/G]GTGAACAAAATGACT | 84954 |
| rs190366008 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MPND | GRCh38.p7 | 19:4347531 | AGTGTGAGCCACCGC[A/G]CCCAGCTGCCTGTAG | 84954 |
| rs190462781 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | MPND | GRCh38.p7 | 19:4351584 | AATAGACTTGGCGGC[C/T]GGGCACGGTGGCTCA | 84954 |
| rs190738938 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | MPND | GRCh38.p7 | 19:4356560 | TAAGAACATAAAAAG[A/T]GAAGGGCTGCTAATA | 84954 |
| rs190873272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4348134 | TGACATCAGGTGATC[C/T]GCCCGCCTCCGCCTC | 84954 |
| rs191139135 | snp | C/G/T | 0.00557542 | 0.0525036 | intron-variant | MPND | GRCh38.p7 | 19:4344831 | GCAACCTCTGCCTCC[C/G/T]GGTTCAAGCGATTTT | 84954 |
| rs191244979 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | MPND | GRCh38.p7 | 19:4348011 | ATTCTCCTGCCTCAG[C/T]CTCGCGAGTAGCTGG | 84954 |
| rs191306061 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MPND | GRCh38.p7 | 19:4353621 | GGGCAGAGTACAGTG[A/G]TGCAATCATGGCTAA | 84954 |
| rs191391230 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | MPND | GRCh38.p7 | 19:4353240 | CTTGACTTCTTAAGC[C/T]CAAATGCTGGATTTT | 84954 |
| rs191724780 | snp | C/G | | | intron-variant | MPND | GRCh38.p7 | 19:4348890 | TTGAACTCCTGACCT[C/G]GTGATCTACCTGCCT | 84954 |
| rs191876093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4358492 | GTTCAACATGCATTT[A/G]AAACACTAAACTAAG | 84954 |
| rs191946555 | snp | C/T | 0.00104617 | 0.0228472 | intron-variant | MPND | GRCh38.p7 | 19:4358185 | ATGGTGAGCTCGCTG[C/T]GGGGCGGGCAGGCAG | 84954 |
| rs192004750 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4352709 | AAATAAAAAATAAAT[G/T]ACAAATAAATAAAAA | 84954 |
| rs192464403 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | MPND | GRCh38.p7 | 19:4351542 | TCCCCGTGGAGTTGG[A/C]GGTCATTGTGCCCTT | 84954 |
| rs192526108 | snp | C/T | 0.000251566 | 0.0112125 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4345773 | TGGGCGACCTGCAGC[C/T]AGACGGAAGGATCAT | 84954 |
| rs192602695 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4346836 | AGAGATCCAGACCAG[C/T]CTGGCCAACATGGTG | 84954 |
| rs192660837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4346229 | GAGCTTTCTAGAAGG[A/G]TGGAATGGCATACGC | 84954 |
| rs192718475 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4349474 | AGTGAGGGTGCTCAA[C/T]GGGAGGCTGCCGAGT | 84954 |
| rs193099915 | snp | A/G | 0.000801296 | 0.0200001 | intron-variant | MPND | GRCh38.p7 | 19:4355046 | CAGGGCCAGGTGGGC[A/G]GGGGCGTTGGAGGAC | 84954 |
| rs193242680 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4357687 | CTCCACTGGAGAGTT[C/G]GGGCCCCAGTTTCTC | 84954 |
| rs199745690 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4350106 | GCTTCACTGAGAAGG[C/T]GACATTTGAACGGAG | 84954 |
| rs199768864 | snp | A/G | 0.000108201 | 0.00735449 | synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4345969 | GCACACGCCTGCCAC[A/G]GCTGCTGATGAGGTA | 84954 |
| rs199788497 | snp | A/G | 9.33838e-05 | 0.00683251 | missense, intron-variant, nc-transcript-variant | MPND | GRCh38.p7 | 19:4358131 | GTGGAGATGGCCTAC[A/G]TCCAGGACAGCTTCC | 84954 |
| rs199844303 | snp | A/G | 5.21553e-05 | 0.00510636 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4354326 | CTGGCCCCTACAGGA[A/G]CCCCCACACCCTGGT | 84954 |
| rs199989643 | snp | C/T | 0.000913863 | 0.0213564 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4353027 | CAGAGCCTGCCCACC[C/T]GGGTGAGAGGCGTGG | 84954 |
| rs200057588 | snp | C/T | 0.00171417 | 0.0292258 | intron-variant | MPND | GRCh38.p7 | 19:4359272 | TGAGCCCCAAGTCCC[C/T]GCAGACCTCCTAACG | 84954 |
| rs200101987 | snp | C/T | 6.71377e-05 | 0.00579348 | synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4345888 | GGGCTGTGGCTGGGC[C/T]TCTGTCAAGTACAAA | 84954 |
| rs200267200 | snp | A/G | 1.8834e-05 | 0.00306865 | intron-variant | MPND | GRCh38.p7 | 19:4357211 | AAGCTCACTAGAGCC[A/G]TTCAGGCCCCTGTGC | 84954 |
| rs200322190 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4360487 | ATGTACTTCTGACGA[C/G]GGGGGTGCAGGGCAG | 84954 |
| rs200374997 | in-del | -/GTTAC | 0.0142736 | 0.0832652 | intron-variant | MPND | GRCh38.p7 | 19:4347634 | AGCAGACCACAAATG[-/GTTAC]GTTATACAAGCTGTG | 84954 |
| rs200397267 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4353570 | ACTGTACCTGTTTTT[C/T]TGTTTTTTTGAGACA | 84954 |
| rs200486806 | snp | C/T | 0.000222437 | 0.0105437 | synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357348 | TCTGCAGGACATCGA[C/T]GCACAGATGGACTAC | 84954 |
| rs200516910 | snp | G/T | | | intron-variant | MPND | GRCh38.p7 | 19:4347897 | ATTGTGTTTTTTTTT[G/T]TTTTTTTTTTTTGAG | 84954 |
| rs200526614 | snp | C/T | 0.00155762 | 0.0278637 | synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4345777 | CGACCTGCAGCCAGA[C/T]GGAAGGATCATGTGG | 84954 |
| rs200894292 | snp | C/T | 0.00399206 | 0.0444982 | synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4345948 | CTGGCTCCGGCTGCA[C/T]CAGCTGCACACGCCT | 84954 |
| rs200906141 | snp | C/T | 0.00130887 | 0.0255484 | intron-variant | MPND | GRCh38.p7 | 19:4355070 | GGAGGACCGGGGTCA[C/T]GGGGTCACAGCTGCC | 84954 |
| rs200972486 | snp | C/T | 0.00134727 | 0.0259195 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4359193 | TTCTACAAGGGTTCC[C/T]CTGACCTCGTGAGGC | 84954 |
| rs200976690 | snp | C/T | 3.67897e-05 | 0.00428877 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4352997 | AGAGTCGGAGACCAC[C/T]GGGGAAGAGCCCTTC | 84954 |
| rs201096146 | snp | C/T | 1.76524e-05 | 0.00297084 | intron-variant, missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4355000 | GGTTACCTGGGGGGC[C/T]GCTGGGACGTCAACA | 84954 |
| rs201171608 | snp | C/T | 0 | 0 | intron-variant | MPND | GRCh38.p7 | 19:4354005 | TAATTTGTTCTAACT[C/T]GGGCTGGGGAGGGAC | 84954 |
| rs201247790 | snp | A/C/G | | | intron-variant | MPND | GRCh38.p7 | 19:4349323 | TCAAGTGATCCACTC[A/C/G]CTTCGGTATCCCAAA | 84954 |
| rs201493632 | snp | G/T | 0.00199793 | 0.0315432 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4345842 | CCTGGGCCACCCACT[G/T]CAAGAAGCTGGTGAA | 84954 |
| rs201494111 | snp | C/G/T | 0.00010228 | 0.00715062 | intron-variant, synonymous-codon, missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4355164 | GACTGCAGCTGCCAT[C/G/T]GAAGAGGAGGTGAGG | 84954 |
| rs201559730 | snp | A/C | 1.83798e-05 | 0.00303143 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4352994 | ACAAGAGTCGGAGAC[A/C]ACTGGGGAAGAGCCC | 84954 |
| rs201566644 | snp | A/G | 0.000122195 | 0.00781553 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357371 | TGGACTACCAGCTGC[A/G]GCTGCAGGGCTCCAG | 84954 |
| rs201571889 | snp | A/G | 0.000354587 | 0.0133104 | synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4353028 | AGAGCCTGCCCACCC[A/G]GGTGAGAGGCGTGGG | 84954 |
| rs201619246 | snp | C/T | 0.00134821 | 0.0259285 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4345968 | TGCACACGCCTGCCA[C/T]GGCTGCTGATGAGGT | 84954 |
| rs201847733 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4356655 | TTTTTTTTTCCTTTT[C/T]TTTGAGACACGATCT | 84954 |
| rs201982212 | snp | C/T | 6.77736e-05 | 0.00582084 | intron-variant, synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4355137 | TTGTCGGAGCCGGCT[C/T]GGGGACGCAGAGACT | 84954 |
| rs202116656 | snp | C/T | 0.000743244 | 0.0192632 | synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357408 | CTTCCAGCCCTGCCT[C/T]GCCCTGCTCTGCTGT | 84954 |
| rs202160249 | in-del | -/A | | | intron-variant | MPND | GRCh38.p7 | 19:4352839 | TGGGATTTAGCAGGG[-/A]GCGGGGGGGCACCCA | 84954 |
| rs202244264 | in-del | -/TT | 0.486529 | 0.0809556 | intron-variant | MPND | GRCh38.p7 | 19:4355858 | CCACTGCGCCCGGCC[-/TT]TTTTTTTTTTTTCTT | 84954 |
| rs367566493 | in-del | -/CGTTA | | | intron-variant | MPND | GRCh38.p7 | 19:4347638 | GACCACAAATGGTTA[-/CGTTA]TACAAGCTGTGAGGT | 84954 |
| rs367569663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4356936 | TGAGCCACTGCTCCC[A/G]GCCTAGTTTTAACTG | 84954 |
| rs367666320 | snp | G/T | | | intron-variant | MPND | GRCh38.p7 | 19:4353255 | TCAAATGCTGGATTT[G/T]ATTTTATTTTATATA | 84954 |
| rs367697549 | snp | C/T | 0.000289031 | 0.012018 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | MPND, SH3GL1 | GRCh38.p7 | 19:4360026 | GGGCAGGGTGGGCTC[C/T]AGTTGTCTTGAGGGT | 84954 |
| rs367800098 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | MPND | GRCh38.p7 | 19:4356546 | CAAGACCCTATATCT[A/C]AGAACATAAAAAGTG | 84954 |
| rs367806014 | snp | A/C | | | intron-variant | MPND | GRCh38.p7 | 19:4347387 | CTGGGACTACAGGCA[A/C]CCACCACCACGCCCG | 84954 |
| rs367902255 | snp | A/G | 1.73507e-05 | 0.00294535 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357544 | GGCAACCCAGGCCCC[A/G]AGTCCAAGATCTCAC | 84954 |
| rs368152281 | snp | A/G | 0.00057262 | 0.016911 | missense, downstream-variant-500B, nc-transcript-variant | MPND, SH3GL1 | GRCh38.p7 | 19:4359979 | CTGGAACAGGTGTGC[A/G]GCGTCCTCAAGCAGG | 84954 |
| rs368200075 | snp | A/G | 0.0103295 | 0.0711199 | downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4360256 | ACCCACCTTGGGCTC[A/G]GGAGCACCTGGGGTG | 84954 |
| rs368253644 | snp | A/C/G | 0.000650119 | 0.0180179 | intron-variant | MPND | GRCh38.p7 | 19:4357484 | CCAGCCGAGCCTCCC[A/C/G]GGGCCAACCCCTCTC | 84954 |
| rs368354022 | snp | A/G | 9.17726e-05 | 0.00677332 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4354406 | GCTGTTTCTAGCAAC[A/G]TGCTGTTCCTGCTGG | 84954 |
| rs368474355 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4354468 | CTCCGGAGCCCAGTC[A/G]GTGGGCAGCGGGCGG | 84954 |
| rs368531109 | snp | A/G | 0.000206334 | 0.010155 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | MPND, SH3GL1 | GRCh38.p7 | 19:4360044 | TTGTCTTGAGGGTCC[A/G]GATGGGCTCAGGTAA | 84954 |
| rs368553086 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4344138 | GAGAGACGAGCCCCG[A/G]TGTGGCGAGGGGAAA | 84954 |
| rs368705731 | snp | A/G | 1.70912e-05 | 0.00292324 | intron-variant, synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4355170 | AGCTGCCATCGAAGA[A/G]GAGGTGAGGGGCTAC | 84954 |
| rs368803417 | snp | C/T | 0.000200568 | 0.0100122 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4345820 | CAGACCTTCAACTCA[C/T]CCAGCGCCTGGGCCA | 84954 |
| rs368983221 | snp | A/C | 1.84756e-05 | 0.00303932 | intron-variant | MPND | GRCh38.p7 | 19:4357243 | CGCTGAGCTGCGCCT[A/C]TGTCCCCAGATCTAC | 84954 |
| rs369114478 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4352796 | ATGTGGGGCAATGGC[A/G]CTTACGGCTTAGGCC | 84954 |
| rs369312074 | snp | G/T | | | intron-variant | MPND | GRCh38.p7 | 19:4345239 | TTTAGTAGAGATGGG[G/T]TTTCACCATGTTGGC | 84954 |
| rs369355184 | snp | A/G | 1.75391e-05 | 0.00296129 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357380 | AGCTGCGGCTGCAGG[A/G]CTCCAGCAATGGCTT | 84954 |
| rs369442146 | in-del | -/T | | | intron-variant | MPND | GRCh38.p7 | 19:4344735 | GGTAGGTATTAGTAC[-/T]TTTTTTTTTTTTTTT | 84954 |
| rs369566363 | snp | G/T | 1.7828e-05 | 0.00298558 | intron-variant | MPND | GRCh38.p7 | 19:4345728 | TCCTGGGCCCAGCCA[G/T]CTGACTGTCACTGCA | 84954 |
| rs369787755 | snp | C/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4360522 | GAGCAGAGCCTGGGG[C/T]CCGGAGGCTTCACTG | 84954 |
| rs369854560 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MPND | GRCh38.p7 | 19:4347365 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 84954 |
| rs369865886 | snp | C/T | 8.7203e-05 | 0.00660257 | intron-variant | MPND | GRCh38.p7 | 19:4355045 | CCAGGGCCAGGTGGG[C/T]GGGGGCGTTGGAGGA | 84954 |
| rs369885008 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4360239 | GCCTCAGGGCCAGTC[C/T]CACCCACCTTGGGCT | 84954 |
| rs369909972 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | MPND | GRCh38.p7 | 19:4348446 | TTGTATTTTTAGTAG[A/T]AATGGGGTTTCACCA | 84954 |
| rs369919524 | snp | A/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4360571 | ATGTGAATGTGGCCT[A/G]GCCCAGAGAACTCCC | 84954 |
| rs369950673 | snp | G/T | 4.08172e-05 | 0.0045174 | intron-variant | MPND | GRCh38.p7 | 19:4357631 | GCCCGGGAGCACTGG[G/T]GCATTTGGGTCACGA | 84954 |
| rs369989865 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4350133 | GGAGAACTGAAGGTG[A/G]GGAGGGAGGGAGGGT | 84954 |
| rs370097973 | snp | A/G | 9.33663e-05 | 0.00683187 | missense, intron-variant, nc-transcript-variant | MPND | GRCh38.p7 | 19:4358116 | GGCATCCCCATGGAT[A/G]TGGAGATGGCCTACG | 84954 |
| rs370107288 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4352051 | GGTGGTGGGCAACTG[C/T]ACTCCCAGCTACTCA | 84954 |
| rs370186418 | snp | G/T | 0.000165986 | 0.00910854 | intron-variant, missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4355005 | CCTGGGGGGCCGCTG[G/T]GACGTCAACAGCCAG | 84954 |
| rs370229309 | snp | A/G | 0.000165986 | 0.00910854 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357419 | GCCTCGCCCTGCTCT[A/G]CTGTACGCGGGATGG | 84954 |
| rs370265336 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4349155 | TCACTGCAACCTCCC[A/G]TTCCCGGGTTCACGC | 84954 |
| rs370388121 | snp | C/G/T | 5.05935e-05 | 0.00502937 | intron-variant, synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4355116 | GACGGTGCTCAGAGC[C/G/T]TTCCCTTGTCGGAGC | 84954 |
| rs370453552 | snp | A/G | | | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342067 | AAAGAAAAAAGAAAA[A/G]AAAAGAAAACAAAAT | 84954 |
| rs370497874 | in-del | -/G | | | intron-variant | MPND | GRCh38.p7 | 19:4352839 | GGGATTTAGCAGGGA[-/G]GCGGGGGGGCACCCA | 84954 |
| rs370625305 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4350473 | TTAGGGTGGGATCCA[A/G]GGACCAGGGCAGAGG | 84954 |
| rs370701936 | snp | C/G/T | 0.00049568 | 0.0157359 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | MPND, SH3GL1 | GRCh38.p7 | 19:4359981 | GGAACAGGTGTGCGG[C/G/T]GTCCTCAAGCAGGGG | 84954 |
| rs370814325 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4356043 | ATTTTTAGTTGAGAC[A/G]GGGTTTCACCATGTT | 84954 |
| rs370837318 | snp | A/G | 1.74154e-05 | 0.00295083 | intron-variant | MPND | GRCh38.p7 | 19:4355042 | TATCCAGGGCCAGGT[A/G]GGCGGGGGCGTTGGA | 84954 |
| rs370907634 | in-del | -/C | | | intron-variant | MPND | GRCh38.p7 | 19:4359649 | TGGGTGTCTGGAACC[-/C]AGGCAGGGAGGGGCT | 84954 |
| rs371005566 | snp | A/G | 0.000109657 | 0.00740382 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4345941 | AGGCCACCTGGCTCC[A/G]GCTGCACCAGCTGCA | 84954 |
| rs371023215 | snp | C/T | 0.000169434 | 0.00920263 | missense, downstream-variant-500B, nc-transcript-variant | MPND, SH3GL1 | GRCh38.p7 | 19:4359935 | CCTTGGCCAGCAGGA[C/T]GCCCAAGGACCAGAG | 84954 |
| rs371067036 | in-del | -/TT | 0.456568 | 0.140818 | intron-variant | MPND | GRCh38.p7 | 19:4347897 | TTGTGTTTTTTTTTG[-/TT]TTTTTTTTTTTTGAG | 84954 |
| rs371154609 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4349451 | GTGGGAGGGATGGAG[C/T]GTCAGGAAGTGAGGG | 84954 |
| rs371185581 | snp | C/T | 7.28146e-05 | 0.00603341 | intron-variant | MPND | GRCh38.p7 | 19:4357462 | AGCAAGGAGGGGGGA[C/T]GCTGGGCCAGCCGAG | 84954 |
| rs371258857 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342466 | CTGAGAACATTCCCG[A/G]GCACCCTGGAGAGCC | 84954 |
| rs371332035 | snp | C/G | | | intron-variant | MPND | GRCh38.p7 | 19:4353042 | CGGGTGAGAGGCGTG[C/G]GGAGGGGAGGCAGGA | 84954 |
| rs371337749 | snp | A/T | | | intron-variant | MPND | GRCh38.p7 | 19:4346593 | GGCTAATTTTTGGAT[A/T]TTTAGAAGAGATGAG | 84954 |
| rs371393082 | snp | A/C/G/T | 0.00102504 | 0.0226196 | missense, synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4359216 | CGTGAGGCTCCAGGA[A/C/G/T]CCCTGGAGCCAGGAG | 84954 |
| rs371699800 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | MPND | GRCh38.p7 | 19:4346473 | CCCAGGCTGGAGTGC[A/G]GTGCCCCCATCTTGG | 84954 |
| rs371779166 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | MPND | GRCh38.p7 | 19:4351924 | ACACCTGTAATGCCA[A/G]CACTTTGGGAGGCTG | 84954 |
| rs371804258 | in-del | -/CCT | | | intron-variant | MPND | GRCh38.p7 | 19:4348370 | GGTTCAAGCGATTCT[-/CCT]GCCTGAGCCTCTTGA | 84954 |
| rs372046727 | snp | A/C/G | | | missense, downstream-variant-500B, nc-transcript-variant | MPND, SH3GL1 | GRCh38.p7 | 19:4359970 | TGTCACGTCCTGGAA[A/C/G]AGGTGTGCGGCGTCC | 84954 |
| rs372060833 | snp | C/G | 0.000103461 | 0.00719164 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | MPND, SH3GL1 | GRCh38.p7 | 19:4360045 | TGTCTTGAGGGTCCG[C/G]ATGGGCTCAGGTAAT | 84954 |
| rs372082024 | snp | A/C | 0.000863931 | 0.0207658 | intron-variant | MPND | GRCh38.p7 | 19:4354600 | GGCCAGGCCCAGTGG[A/C]TCACACCTATAATCC | 84954 |
| rs372226495 | snp | A/G | 0.000320736 | 0.0126596 | intron-variant | MPND | GRCh38.p7 | 19:4354457 | GGGGCAAGGGGCTCC[A/G]GAGCCCAGTCGGTGG | 84954 |
| rs372254296 | snp | C/T | 5.03149e-05 | 0.00501547 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4354095 | ATCCGGGTTCCGGTC[C/T]GCTACTGCATGCTGG | 84954 |
| rs372264614 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | MPND | GRCh38.p7 | 19:4354298 | TGGGGATTCCTGAGA[C/T]TGTGCGACCCTCCTG | 84954 |
| rs372461986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4357720 | TCTATGAAATGGGGA[C/T]GTGACTGCTGCCCTG | 84954 |
| rs372519061 | snp | C/G | 0.000869622 | 0.020834 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4343769 | GGAGGAGGACGAGGA[C/G]GAAGCGGAGGCCGAG | 84954 |
| rs372726989 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | MPND | GRCh38.p7 | 19:4347761 | AACCCATGAACCTGC[C/T]CGACGCAGTGGCAAA | 84954 |
| rs372780046 | snp | A/C | | | intron-variant | MPND | GRCh38.p7 | 19:4351668 | ACGATCGAGACCATC[A/C]TGGCTAACACGGTGA | 84954 |
| rs372822657 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4350587 | TTTTGGAAGTGTATC[C/T]GCCAGATTTGCTGAT | 84954 |
| rs372885603 | snp | A/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4360525 | CAGAGCCTGGGGTCC[A/G]GAGGCTTCACTGGAC | 84954 |
| rs372917252 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4358956 | TGGCAGCCACTTGGG[C/T]AACGCTGCTGCCTCC | 84954 |
| rs372988573 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4350533 | GGAGTGGCCCAGGCC[A/G]ACCATGGAGCAGGGA | 84954 |
| rs373057898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4358283 | ATGGCTGGTGGCGCC[C/T]TGGGGGCCTGGGTTA | 84954 |
| rs373102998 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | MPND | GRCh38.p7 | 19:4352801 | GGGCAATGGCACTTA[C/T]GGCTTAGGCCAAAGG | 84954 |
| rs373170775 | snp | A/T | | | intron-variant | MPND | GRCh38.p7 | 19:4346862 | TGGTGAAACCCCGTC[A/T]CTACTAAAAAGACAA | 84954 |
| rs373286625 | snp | C/T | 0.00575038 | 0.0533116 | intron-variant, nc-transcript-variant | MPND | GRCh38.p7 | 19:4358041 | AGCTGCCATGGGCTG[C/T]GGGCTGGTGAGGCTT | 84954 |
| rs373332702 | snp | G/T | 1.93639e-05 | 0.00311152 | intron-variant | MPND | GRCh38.p7 | 19:4354927 | GCCTGAGCCAGTCTT[G/T]TGCTGTTCCTCCCTT | 84954 |
| rs373394568 | snp | C/T | 3.51136e-05 | 0.00418994 | intron-variant, synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4355008 | GGGGGGCCGCTGGGA[C/T]GTCAACAGCCAGAGT | 84954 |
| rs373507634 | snp | A/C | | | intron-variant | MPND | GRCh38.p7 | 19:4351976 | TCAGGAGTTTGAGAC[A/C]AGCCTGGCCAACATG | 84954 |
| rs373511508 | snp | A/G | 1.66482e-05 | 0.0028851 | synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4359168 | TGTCCTGTAGATGCT[A/G]CTGGTGGAGTTCTAC | 84954 |
| rs373654341 | snp | G/T | 0.000163987 | 0.00905353 | intron-variant | MPND | GRCh38.p7 | 19:4354012 | TTCTAACTTGGGCTG[G/T]GGAGGGACTGACCCT | 84954 |
| rs373658173 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | MPND | GRCh38.p7 | 19:4355430 | AAGCTCCGCCTCCCG[G/T]GTTCACGCCATTCTC | 84954 |
| rs373702170 | snp | A/G/T | 2.09286e-05 | 0.00323479 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4352898 | CCTAACCCCTGCAGA[A/G/T]CCCAGCCAGTGAAGG | 84954 |
| rs373705307 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | MPND | GRCh38.p7 | 19:4356854 | CATGTTGGCCAGGCT[A/G]GTCTTGAACTCGTGA | 84954 |
| rs373715689 | in-del | -/AAAAG | 0.00119737 | 0.0244387 | intron-variant | MPND | GRCh38.p7 | 19:4352191 | GAAAAAAAAAAAGAT[-/AAAAG]AATAGATAGAGTTCA | 84954 |
| rs373733628 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4353859 | TGTAAATAAGAGTCT[C/T]ACTCTGTAACTCAGG | 84954 |
| rs373741270 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4343681 | CGTGGGGCGAGCGGC[C/T]TCCCTGCAGCCTCTC | 84954 |
| rs373805742 | snp | A/C | 0.000262962 | 0.0114635 | stop-lost, downstream-variant-500B, nc-transcript-variant | MPND, SH3GL1 | GRCh38.p7 | 19:4360002 | CAAGCAGGGGAGCTG[A/C]GCCTTCCAGGGCAGG | 84954 |
| rs373830032 | snp | C/T | 0.00010158 | 0.00712597 | intron-variant, missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4355132 | TTCCCTTGTCGGAGC[C/T]GGCTCGGGGACGCAG | 84954 |
| rs373896278 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4352653 | CACACCACTGCACTC[C/T]AGACTGGGCGACAGA | 84954 |
| rs374021802 | snp | A/G | 0.000124457 | 0.00788751 | intron-variant | MPND | GRCh38.p7 | 19:4357510 | CTCTCCCTCTCTCCC[A/G]CCAGCCCCTTACTAT | 84954 |
| rs374039775 | snp | G/T | | | intron-variant | MPND | GRCh38.p7 | 19:4353094 | TTGGGGAGGAGACTG[G/T]GGAGAGGTTGGGCCT | 84954 |
| rs374051280 | snp | A/G | | | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342562 | TGAGCCCATCCCACG[A/G]CGTCCCGGAGCTTTA | 84954 |
| rs374181373 | snp | A/C | 0.000200404 | 0.0100082 | intron-variant | MPND | GRCh38.p7 | 19:4357449 | GGGCTGTGGGGGGAG[A/C]AAGGAGGGGGGATGC | 84954 |
| rs374413421 | snp | A/C/G | | | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342077 | GAAAAGAAAAGAAAA[A/C/G]AAAATAATAATATGG | 84954 |
| rs374446819 | snp | C/T | 1.68476e-05 | 0.00290233 | intron-variant | MPND | GRCh38.p7 | 19:4359261 | CAAGCTTAAGGTGAG[C/T]CCCAAGTCCCCGCAG | 84954 |
| rs374599119 | snp | A/C/G | 1.70542e-05 | 0.00292007 | intron-variant, missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4355165 | ACTGCAGCTGCCATC[A/C/G]AAGAGGAGGTGAGGG | 84954 |
| rs374649439 | in-del | -/CTC | 0.00597247 | 0.0543191 | intron-variant | MPND | GRCh38.p7 | 19:4348368 | CAGGTTCAAGCGATT[-/CTC]CTGCCTGAGCCTCTT | 84954 |
| rs374785675 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | MPND | GRCh38.p7 | 19:4358671 | GGGTGCCTATAGTCC[C/T]AGCTACTTGGGAGGC | 84954 |
| rs375011849 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant, utr-variant-3-prime, downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4360583 | CCTGGCCCAGAGAAC[C/T]CCCCATTTCATCGAT | 84954 |
| rs375078562 | snp | A/G | 0.000161987 | 0.00899818 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | MPND, SH3GL1 | GRCh38.p7 | 19:4359966 | CCTGTGTCACGTCCT[A/G]GAACAGGTGTGCGGC | 84954 |
| rs375120386 | snp | A/T | | | intron-variant | MPND | GRCh38.p7 | 19:4356176 | TGCTTTTGGATCTCC[A/T]AGCCCTGGTGCTGAA | 84954 |
| rs375122546 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4349485 | TCAACGGGAGGCTGC[C/T]GAGTCCTCAGTGGCT | 84954 |
| rs375130729 | snp | C/T | | | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4354338 | GGAACCCCCACACCC[C/T]GGTGGAAGTAACATC | 84954 |
| rs375265692 | in-del | -/AAG | | | intron-variant | MPND | GRCh38.p7 | 19:4346798 | CATTTTGGGAGGCTG[-/AAG]CAGGCAGGTTCACGA | 84954 |
| rs375270571 | snp | C/T | 0.000437904 | 0.0147905 | synonymous-codon, intron-variant, nc-transcript-variant | MPND | GRCh38.p7 | 19:4358166 | CAATGACATCCTTCA[C/T]GAGATGGTGAGCTCG | 84954 |
| rs375446175 | snp | C/T | 0.000516022 | 0.0160544 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | MPND, SH3GL1 | GRCh38.p7 | 19:4360043 | GTTGTCTTGAGGGTC[C/T]GGATGGGCTCAGGTA | 84954 |
| rs375486549 | snp | A/C | 5.48953e-05 | 0.00523876 | intron-variant | MPND | GRCh38.p7 | 19:4345721 | GTGTTGGTCCTGGGC[A/C]CAGCCAGCTGACTGT | 84954 |
| rs375547359 | snp | C/T | 3.76989e-05 | 0.00434143 | intron-variant | MPND | GRCh38.p7 | 19:4357210 | TAAGCTCACTAGAGC[C/T]GTTCAGGCCCCTGTG | 84954 |
| rs375676071 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4359105 | GAACCCCAGGAGAGG[C/T]GCTGAGGTACCTCAG | 84954 |
| rs375734023 | snp | A/C/G | 0.000180443 | 0.00949699 | intron-variant | MPND | GRCh38.p7 | 19:4357491 | AGCCTCCCAGGGCCA[A/C/G]CCCCTCTCCCTCTCT | 84954 |
| rs375759802 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4350730 | TGACCCTGTGAGTCC[C/T]CCACATGGAGACATA | 84954 |
| rs375783081 | snp | C/T | 1.82075e-05 | 0.00301719 | intron-variant | MPND | GRCh38.p7 | 19:4357473 | GGGATGCTGGGCCAG[C/T]CGAGCCTCCCAGGGC | 84954 |
| rs375798863 | snp | A/G | 2.84629e-05 | 0.00377235 | intron-variant | MPND | GRCh38.p7 | 19:4357601 | GTAGGTGGGGCTGTT[A/G]GGAGAGCCTGGGGGG | 84954 |
| rs375847025 | snp | C/G | | | intron-variant | MPND | GRCh38.p7 | 19:4350457 | ACTAGACTGTCGGGG[C/G]TTAGGGTGGGATCCA | 84954 |
| rs375908042 | snp | C/T | 3.41676e-05 | 0.00413311 | missense, intron-variant, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357335 | CGGCGCTGCCATCTC[C/T]GCAGGACATCGACGC | 84954 |
| rs375911721 | in-del | -/AAG | 0.00438332 | 0.0466095 | intron-variant | MPND | GRCh38.p7 | 19:4351566 | TGCCCTTTTACAGAT[-/AAG]AATAGACTTGGCGGC | 84954 |
| rs375953534 | snp | C/T | 3.71837e-05 | 0.00431167 | intron-variant | MPND | GRCh38.p7 | 19:4357238 | GTGCCCGCTGAGCTG[C/T]GCCTCTGTCCCCAGA | 84954 |
| rs376039143 | snp | A/G/T | 0.00288565 | 0.0378748 | intron-variant | MPND | GRCh38.p7 | 19:4355071 | GAGGACCGGGGTCAC[A/G/T]GGGTCACAGCTGCCC | 84954 |
| rs376145951 | snp | A/C/G/T | 0.000186578 | 0.00965701 | intron-variant, missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4355138 | TGTCGGAGCCGGCTC[A/C/G/T]GGGACGCAGAGACTG | 84954 |
| rs376188009 | snp | A/G | 0.000348614 | 0.0131979 | synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357366 | ACAGATGGACTACCA[A/G]CTGCGGCTGCAGGGC | 84954 |
| rs376253534 | snp | A/G/T | 0.000104964 | 0.00724368 | synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4345960 | GCACCAGCTGCACAC[A/G/T]CCTGCCACGGCTGCT | 84954 |
| rs376470885 | snp | C/T | 1.78931e-05 | 0.00299102 | intron-variant, synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4354981 | GACACGGAGTGAGGT[C/T]GTGGGTTACCTGGGG | 84954 |
| rs376489414 | snp | C/G | | | intron-variant | MPND | GRCh38.p7 | 19:4357682 | CCAGGCTCCACTGGA[C/G]AGTTGGGGCCCCAGT | 84954 |
| rs376496528 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | MPND | GRCh38.p7 | 19:4348172 | GCTGGGATTACAGGC[G/T]TGAGCCACCAAGCCC | 84954 |
| rs376515956 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4357820 | TCCCTTCCTGACCCT[A/G]CCTGGCTTCATTCCC | 84954 |
| rs376592703 | snp | C/T | 0.000163987 | 0.00905353 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4354108 | TCCGCTACTGCATGC[C/T]GGGCAGCCGCGACTT | 84954 |
| rs376636031 | snp | C/G | | | intron-variant | MPND | GRCh38.p7 | 19:4348321 | GCTGGAGCTCAGTGG[C/G]ACAATCTAGGCTCAC | 84954 |
| rs376642769 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | MPND | GRCh38.p7 | 19:4348299 | GGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGCT | 84954 |
| rs376700105 | snp | C/G/T | 0.000100309 | 0.0070814 | synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4345810 | GGAGACCGGGCAGAC[C/G/T]TTCAACTCACCCAGC | 84954 |
| rs376707936 | snp | C/G/T | 1.89295e-05 | 0.00307643 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4352929 | GGAGGAGGAGGAGTT[C/G/T]CTGATGGAAGAGGAG | 84954 |
| rs376774756 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4348845 | TATTTTTAGTGGAGA[C/T]GGGGTTTCACCATTT | 84954 |
| rs376863181 | snp | C/T | 0.000171985 | 0.00927162 | intron-variant | MPND | GRCh38.p7 | 19:4354467 | GCTCCGGAGCCCAGT[C/T]GGTGGGCAGCGGGCG | 84954 |
| rs377009017 | snp | C/G | 1.81066e-05 | 0.00300882 | intron-variant | MPND | GRCh38.p7 | 19:4357455 | TGGGGGGAGCAAGGA[C/G]GGGGGATGCTGGGCC | 84954 |
| rs377017388 | in-del | -/CA | 0.0023933 | 0.0345097 | intron-variant | MPND | GRCh38.p7 | 19:4357694 | GGAGAGTTGGGGCCC[-/CA]GTTTCTCCATCTATG | 84954 |
| rs377098672 | snp | A/G | 7.09031e-05 | 0.0059537 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357409 | TTCCAGCCCTGCCTC[A/G]CCCTGCTCTGCTGTA | 84954 |
| rs377190805 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | MPND | GRCh38.p7 | 19:4357049 | TTTGTGGCAGGGTGC[A/G]TCTTTTATATTAAAA | 84954 |
| rs377264342 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | MPND | GRCh38.p7 | 19:4358237 | GCACACGATGCGTTG[C/G]TCTGCTTCCCACCGG | 84954 |
| rs377426285 | snp | A/G | 0.000209545 | 0.0102337 | intron-variant | MPND | GRCh38.p7 | 19:4355025 | TCAACAGCCAGAGTG[A/G]GTATCCAGGGCCAGG | 84954 |
| rs377641547 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | MPND | GRCh38.p7 | 19:4350991 | TCCTGGTAGGTAGGA[C/G]GCTGTGCTGGGTCAG | 84954 |
| rs377692575 | snp | A/T | | | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342423 | AGTTCACATGTACCC[A/T]GCTCTTGCTCTATGT | 84954 |
| rs377739354 | snp | C/T | 1.79351e-05 | 0.00299454 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4345937 | TACAAGGCCACCTGG[C/T]TCCGGCTGCACCAGC | 84954 |
| rs386388423 | in-del | -/TTT | | | intron-variant | MPND | GRCh38.p7 | 19:4355337 | GTGAAGAACACTGCT[-/TTT]TTTTTTTTTTTTTTT | 84954 |
| rs386388424 | in-del | -/TTT | | | intron-variant | MPND | GRCh38.p7 | 19:4355351 | TTTTTTTTTTTTTTT[-/TTT]TTGAGACGGAGTCTC | 84954 |
| rs386806119 | multinucleotide-polymorphism | AG/CA | | | intron-variant | MPND | GRCh38.p7 | 19:4347068 | AATGGAGATGGTACC[AG/CA]TGCCCATGTGTGGAA | 84954 |
| rs397962827 | in-del | -/G | | | intron-variant | MPND | GRCh38.p7 | 19:4352848 | CAGGGAGCGGGGGGG[-/G]CACCCAGCTGAGGGT | 84954 |
| rs527386856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4359364 | CAGGGGCCTGAGACA[A/G]CCCAGCTGGCAGACT | 84954 |
| rs527437706 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4353989 | ACACCCAGTGGCCAC[A/C]TAATTTGTTCTAACT | 84954 |
| rs527494813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4349423 | GGAAAGCAGTGGTGG[C/T]GGGAGAAGGCGAGTG | 84954 |
| rs527497406 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342866 | AACTAAGGGTTTCTA[C/T]TGATTGGTTTACATG | 84954 |
| rs527609548 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4343229 | AAGTGCGGTGACCGC[A/T]GGTCTCACCTTCTCC | 84954 |
| rs527756531 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MPND | GRCh38.p7 | 19:4358752 | AGATCACGCCACTGC[A/G]CTCCAGTCTGGGCCA | 84954 |
| rs527763222 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4352882 | ACCGCTGTCCCTGAC[C/G]CCTAACCCCTGCAGA | 84954 |
| rs527820448 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MPND | GRCh38.p7 | 19:4353403 | CTCCCAAATAGCTGG[G/T]ACTATAGGCGCCAGC | 84954 |
| rs527841670 | snp | A/G | 0.0138799 | 0.0821421 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342188 | GGAGGCCTGAGACTC[A/G]CTGCGATGGCCAGGA | 84954 |
| rs527895919 | snp | A/G | 0.00172818 | 0.0293446 | missense, downstream-variant-500B, nc-transcript-variant | MPND, SH3GL1 | GRCh38.p7 | 19:4359982 | GAACAGGTGTGCGGC[A/G]TCCTCAAGCAGGGGA | 84954 |
| rs528043818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4356168 | AAGAGCACTGCTTTT[A/G]GATCTCCTAGCCCTG | 84954 |
| rs528213003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4351531 | CCCTGATGCCATCCC[C/T]GTGGAGTTGGAGGTC | 84954 |
| rs528438259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4350383 | GGAGTGTTGCAGGCA[A/G]AGGAAGGACAGGATC | 84954 |
| rs528775556 | snp | C/T | 0.000162785 | 0.00902032 | intron-variant, missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4354970 | CACAGTCACCTGACA[C/T]GGAGTGAGGTCGTGG | 84954 |
| rs528958200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4355484 | GGGACTACAGGTGCC[C/T]GCCACCACGCCCAGC | 84954 |
| rs528995125 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4356056 | ACAGGGTTTCACCAT[A/G]TTGGCCAGGCTGGTT | 84954 |
| rs529262141 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4354825 | GCCAAGATCGTGCCA[C/T]TGCCCTCCAGCCTGG | 84954 |
| rs529374359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4349864 | TAGATATGAATCACA[C/T]GTAACAAATGCCATC | 84954 |
| rs529459102 | in-del | -/TTC | 0.0130921 | 0.0798413 | intron-variant | MPND | GRCh38.p7 | 19:4348661 | CATTTTTCTGTTGAA[-/TTC]TTTTTTTTTTTTGAG | 84954 |
| rs529570283 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4354209 | AGCAAGGGCAGGGGT[C/G]GGGGGTGGGACAGAG | 84954 |
| rs529610547 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MPND | GRCh38.p7 | 19:4352262 | CTTTGAATTTTTGCA[A/G]TCAGACCTTGGCGAT | 84954 |
| rs529670714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4347655 | TTATACAAGCTGTGA[A/G]GTTTTTAAACTTGTG | 84954 |
| rs529994385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4357162 | CCCAGGCCTGATACA[C/T]AGCAGGAATTCGTTC | 84954 |
| rs530042159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4351819 | GTGAGCCGAGATCAT[A/G]CCACTGCACTCCAGC | 84954 |
| rs530056090 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4357679 | GTTCCAGGCTCCACT[G/T]GAGAGTTGGGGCCCC | 84954 |
| rs530394892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4357152 | TCACTGTGTCCCCAG[A/G]CCTGATACACAGCAG | 84954 |
| rs530404251 | snp | C/T | 7.01164e-05 | 0.00592058 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4345929 | TGGACAAGTACAAGG[C/T]CACCTGGCTCCGGCT | 84954 |
| rs530419241 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4355810 | TGATCTGCCCACCTC[A/G]GTCTCCCAAAGTGCT | 84954 |
| rs530564295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4347187 | CGCCTTCAACTGATT[A/G]GATGAGGCCCACCTG | 84954 |
| rs530623791 | snp | G/T | | | intron-variant | MPND | GRCh38.p7 | 19:4353286 | TTTATTTATTTTTTG[G/T]TGATGGAGTCTCCCT | 84954 |
| rs530841509 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MPND | GRCh38.p7 | 19:4356665 | CTTTTCTTTGAGACA[C/T]GATCTTGCTCTGTTG | 84954 |
| rs530861604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4348138 | ATCAGGTGATCCGCC[C/T]GCCTCCGCCTCCCAA | 84954 |
| rs530966725 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4358747 | AGCCGAGATCACGCC[A/G]CTGCGCTCCAGTCTG | 84954 |
| rs531104378 | snp | A/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4360472 | ATCTCTGCGCCCCTC[A/G]TGTACTTCTGACGAG | 84954 |
| rs531212187 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4350463 | CTGTCGGGGGTTAGG[G/T]TGGGATCCAGGGACC | 84954 |
| rs531312978 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MPND | GRCh38.p7 | 19:4358251 | GGTCTGCTTCCCACC[A/G]GTGGGCTTGGGAAGC | 84954 |
| rs531378930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4352843 | ATTTAGCAGGGAGCG[A/G]GGGGGCACCCAGCTG | 84954 |
| rs531503365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4349552 | TGTCGCTCTTGTTGC[C/T]CAGGCTGGAGCGCAA | 84954 |
| rs531617054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4353248 | CTTAAGCTCAAATGC[C/T]GGATTTTATTTTATT | 84954 |
| rs531684026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4348986 | ATGGATACAGTCCTC[A/G]GTGCCAGCAGGAAGC | 84954 |
| rs532226233 | in-del | -/G | 0.00119784 | 0.0244435 | intron-variant | MPND | GRCh38.p7 | 19:4356828 | ATTTTTAGTAGAGAA[-/G]GGGGTTTCTCCATGT | 84954 |
| rs532313306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4357704 | GGCCCCAGTTTCTCC[A/G]TCTATGAAATGGGGA | 84954 |
| rs532426316 | snp | A/T | 9.54335e-05 | 0.00690707 | intron-variant | MPND | GRCh38.p7 | 19:4358195 | CGCTGCGGGGCGGGC[A/T]GGCAGGGGCTGGCAG | 84954 |
| rs532523741 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4351684 | TGGCTAACACGGTGA[A/G]ACCCCATCTCTACTA | 84954 |
| rs532881866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4359721 | CCTCCACACAGCACC[A/G]CTGCCCCTGGGAGCC | 84954 |
| rs532897072 | in-del | -/TC | 0.00597247 | 0.0543191 | intron-variant | MPND | GRCh38.p7 | 19:4356648 | TTCTTTTTTTTTTTT[-/TC]CCTTTTCTTTGAGAC | 84954 |
| rs533055233 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | MPND, SH3GL1 | GRCh38.p7 | 19:4360085 | GAAGCAGCAGCCAGC[C/T]ACGCTGGTCTCCCCA | 84954 |
| rs533170195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4344166 | AAACTGAGGCCCGGG[A/G]CTCCGTTGACTGCAG | 84954 |
| rs533315182 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4349168 | CCGTTCCCGGGTTCA[C/T]GCAATTCTTCTGCGT | 84954 |
| rs533329793 | snp | C/T | 0.000250177 | 0.0111815 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4359217 | GTGAGGCTCCAGGAA[C/T]CCTGGAGCCAGGAGC | 84954 |
| rs533466951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4358812 | CCCAACAAAACCTAA[A/G]CTAGTTCGTCAAACC | 84954 |
| rs533508916 | in-del | -/TTT/TTTT | 0.437118 | 0.165792 | intron-variant | MPND | GRCh38.p7 | 19:4355336 | GGTGAAGAACACTGC[-/TTT/TTTT]TTTTTTTTTTTTTTT | 84954 |
| rs533799945 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4358538 | CACGCCTGTAATCCC[A/C]GCACTTTGGGAGGCT | 84954 |
| rs533866446 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | MPND | GRCh38.p7 | 19:4358939 | TCCAGGTGGACCTCT[C/T]GTGGCAGCCACTTGG | 84954 |
| rs533879926 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4353835 | CCCAGTGAAAAAAAA[A/T]TTCTTCTTTGTAAAT | 84954 |
| rs533906327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4352423 | GGTGCGGTGGCTTAC[A/G]CCTGTAATCCCAGCA | 84954 |
| rs534079857 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MPND | GRCh38.p7 | 19:4344708 | CCTGCCACATGGTAA[A/G]CACTTTATCTGTGGT | 84954 |
| rs534214483 | snp | C/G | 1.71064e-05 | 0.00292454 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357350 | TGCAGGACATCGACG[C/G]ACAGATGGACTACCA | 84954 |
| rs534343048 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4348549 | TAGGCGTGAGCCATC[A/G]CGCCCGGCCTAAATT | 84954 |
| rs534358520 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | MPND | GRCh38.p7 | 19:4344108 | GGGGACACTGAGGCC[C/T]GGAGCTCCCTTGCTG | 84954 |
| rs534421921 | snp | G/T | | | intron-variant | MPND | GRCh38.p7 | 19:4351605 | CGGTGGCTCACGCCT[G/T]TAATCCCAGCACTTT | 84954 |
| rs534462300 | snp | C/T | 0.000151325 | 0.0086971 | intron-variant | MPND | GRCh38.p7 | 19:4346010 | CCTCCTCCAGGAAGC[C/T]GCCCAGGTCACTGTG | 84954 |
| rs534512469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4352063 | CTGTACTCCCAGCTA[C/T]TCAGGAGGCTGAGGC | 84954 |
| rs534545049 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4356143 | AGGTGTGAGCCACCG[C/T]GCCCAGCCTAAGAGC | 84954 |
| rs534597197 | snp | A/G | 3.37958e-05 | 0.00411056 | intron-variant, synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4355128 | AGCCTTCCCTTGTCG[A/G]AGCCGGCTCGGGGAC | 84954 |
| rs534617926 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4350199 | GCCCTGGGGCACGAC[C/T]GTGCCTGGTGTGTTG | 84954 |
| rs534695217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4345325 | GTGCTGGGATTACAG[A/G]CGTGAACCACTGCAC | 84954 |
| rs534999022 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | MPND | GRCh38.p7 | 19:4356093 | TCCTGACCTCGTGAT[-/C]CACCCGCGTCAGCCT | 84954 |
| rs535096247 | snp | C/G | | | intron-variant | MPND | GRCh38.p7 | 19:4348484 | CCGGCTGTTCTCAAA[C/G]TCCTGACCTCGTGAT | 84954 |
| rs535150829 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4353385 | CGATTCTCCTGCCTC[A/G]GCCTCCCAAATAGCT | 84954 |
| rs535187606 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4356666 | TTTTCTTTGAGACAC[A/G]ATCTTGCTCTGTTGC | 84954 |
| rs535198302 | snp | A/G | 8.88533e-05 | 0.00666474 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4354364 | ACATCCTTTGCAGCC[A/G]TCAACAAGTTCCAGC | 84954 |
| rs535306277 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MPND | GRCh38.p7 | 19:4349540 | TTTGAGATGGAGTGT[C/T]GCTCTTGTTGCCCAG | 84954 |
| rs535352553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4359465 | AGCTCCGGCAGTGCC[A/G]GATGAGGTCCTGGCA | 84954 |
| rs535364264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4359808 | CCAGCCCTGTGCCTC[A/G]GTCTCAGGGGGGCTC | 84954 |
| rs535369150 | snp | A/G | 0.000798403 | 0.0199641 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4343600 | GGCGCGGCCATGGCA[A/G]GTACGGCGGGCCCAG | 84954 |
| rs535431975 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4343004 | AATGGGACTCTTATC[A/T]TTGGCTGGCGGGCTC | 84954 |
| rs535509548 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4350138 | ACTGAAGGTGGGGAG[C/G]GAGGGAGGGTGCCAT | 84954 |
| rs535541155 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4343300 | GGCTTCCACCTTGCA[A/G]CCTCTATCCCTGGAC | 84954 |
| rs535549159 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4341593 | TAGCCAGGCATGCTG[G/T]TCACGCCTGTTGTCT | 84954 |
| rs535582494 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | MPND | GRCh38.p7 | 19:4344666 | AAAATTAGGGGATGG[A/T]TAAATGAATAAAGCC | 84954 |
| rs535748251 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4356682 | ATCTTGCTCTGTTGC[C/T]CAGGCTGGACTGCAG | 84954 |
| rs535756464 | snp | A/G | 0.00119856 | 0.0244508 | intron-variant | MPND | GRCh38.p7 | 19:4349172 | TCCCGGGTTCACGCA[A/G]TTCTTCTGCGTCAGC | 84954 |
| rs536080903 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MPND | GRCh38.p7 | 19:4358888 | GGCCACGTCAGGCCC[A/G]CGTGGTTCTGGAGAA | 84954 |
| rs536144640 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MPND | GRCh38.p7 | 19:4353626 | GAGTACAGTGGTGCA[A/G]TCATGGCTAACTGCA | 84954 |
| rs536192561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4346691 | CAAAGTGTTGGGATT[A/G]CGGGCGTGAGCTACT | 84954 |
| rs536619618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4352596 | GGCTGAGGCAGGAGA[A/G]TCACTTGAACCCAGG | 84954 |
| rs536622166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4346061 | GGCACAGCTCTCTCC[A/G]GAGGAGGTATTAGTA | 84954 |
| rs536649565 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4347965 | GCCACGATCTCTGCT[C/T]ATTGCAACCTCTGCC | 84954 |
| rs536732047 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MPND | GRCh38.p7 | 19:4346654 | ACTCCTGGCCTCCAG[C/T]AATCCTCCCACCTGG | 84954 |
| rs536751636 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4356317 | CAGCACTTAGGGAGG[A/C]CGAGGCAGGAGGTTT | 84954 |
| rs536793258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4345157 | GTTCAAGCAATTCTC[C/T]TGCCTTAGCCTCTTG | 84954 |
| rs537155700 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4345203 | AGGCACCCGCCACCA[C/T]GCCTGGCTAATTTTT | 84954 |
| rs537219366 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MPND | GRCh38.p7 | 19:4343663 | GGCGCGGGGCTGCAG[A/G]GCCGTGGGGCGAGCG | 84954 |
| rs537289205 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MPND | GRCh38.p7 | 19:4355612 | AGTGCTGGGATTACA[A/G]GCGTGAGCCACCGTG | 84954 |
| rs537878515 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MPND | GRCh38.p7 | 19:4347515 | AAGTGCTGGGATTAC[A/G]AGTGTGAGCCACCGC | 84954 |
| rs538012290 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4347904 | TTTTTTTTGTTTTTT[G/T]TTTTTGAGACAGACT | 84954 |
| rs538538062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4347397 | AGGCACCCACCACCA[C/T]GCCCGGATAATTTTT | 84954 |
| rs538792541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4349295 | TGGTCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 84954 |
| rs538796318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4346890 | CAAAAATTAGCCAGG[C/T]GTGGTGGTGCACGCC | 84954 |
| rs539129729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4356841 | AAGGGGGTTTCTCCA[C/T]GTTGGCCAGGCTAGT | 84954 |
| rs539376262 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4359050 | TCTTTGTGGTTGGTT[G/T]GTTAGTGATGGGGTC | 84954 |
| rs539529549 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MPND | GRCh38.p7 | 19:4349100 | TGAGATGGAGTCTCG[C/G]TCTGTTGTCCAGGCT | 84954 |
| rs539534713 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4354541 | TGCTTTGTTTGCTAC[A/T]GGTACACTGTGGGTG | 84954 |
| rs539543113 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342531 | CGACTGCGGTCTGGG[A/C]AAAGCCACCCGCACT | 84954 |
| rs539546646 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MPND | GRCh38.p7 | 19:4349564 | TGCCCAGGCTGGAGC[A/G]CAATGGCGTGATCTT | 84954 |
| rs539675983 | snp | A/G | 0.00145507 | 0.0269336 | intron-variant, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357978 | GTGCAGAGCTGAGCC[A/G]GGGTGTGCACTCTCC | 84954 |
| rs539958984 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342196 | GAGACTCACTGCGAT[A/G]GCCAGGATTTGGGTG | 84954 |
| rs539966581 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342941 | TTGACACGGATTGGT[C/T]GGTGCGGGAATCCAG | 84954 |
| rs540006619 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | MPND | GRCh38.p7 | 19:4352842 | GATTTAGCAGGGAGC[C/G]GGGGGGCACCCAGCT | 84954 |
| rs540328275 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4348934 | TGCTGGGATTATAGG[C/T]GTGAGCCACCATGCC | 84954 |
| rs540341901 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | MPND | GRCh38.p7 | 19:4359814 | CTGTGCCTCGGTCTC[-/AG]GGGGGCTCAGTCAGG | 84954 |
| rs540456488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4357040 | TGTCCTGGCTTTGTG[A/G]CAGGGTGCATCTTTT | 84954 |
| rs540534016 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4346276 | GAAGAAAGACCTGCT[A/G]GTGTCATGGGTGGCT | 84954 |
| rs540575432 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | MPND | GRCh38.p7 | 19:4347069 | ATGGAGATGGTACCA[A/G]TGCCCATGTGTGGAA | 84954 |
| rs540853406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4351453 | TATGTATGGTGCTGG[C/T]TCGCTCAATGAACGG | 84954 |
| rs540899242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4349433 | GGTGGCGGGAGAAGG[C/T]GAGTGGGAGGGATGG | 84954 |
| rs541086647 | snp | A/C | | | intron-variant | MPND | GRCh38.p7 | 19:4349696 | TTGTATTTTTAGTAG[A/C]GATGGGGTTTCACCA | 84954 |
| rs541148912 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4359494 | CAGCGGGTTTTGGGA[A/G]TGGCTCCCCTGCAGA | 84954 |
| rs541148929 | snp | A/G | 1.71217e-05 | 0.00292584 | intron-variant | MPND | GRCh38.p7 | 19:4353996 | GTGGCCACCTAATTT[A/G]TTCTAACTTGGGCTG | 84954 |
| rs541424035 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | MPND | GRCh38.p7 | 19:4349631 | TTCTCCTGCCTCAGC[C/G]TCCTGAGTAGCTGGG | 84954 |
| rs541572363 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342678 | GGGTCGGGGATGTAG[C/T]TGCAGAAACAGGGTA | 84954 |
| rs541649544 | snp | G/T | 1.67843e-05 | 0.00289687 | intron-variant | MPND | GRCh38.p7 | 19:4359129 | ACCTCAGGCTTGGAG[G/T]GAGCCTGGGAGTCCA | 84954 |
| rs541684894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4353336 | GCAGTGGCTCAATCT[C/T]GGCTCACTGCAACCT | 84954 |
| rs541692647 | snp | A/G | 3.32165e-05 | 0.00407519 | intron-variant | MPND | GRCh38.p7 | 19:4357615 | TGGGAGAGCCTGGGG[A/G]GCCCGGGAGCACTGG | 84954 |
| rs541790212 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MPND | GRCh38.p7 | 19:4353187 | GCCGGACGAGGCCTG[A/G]GCTGAAGACAGTCCC | 84954 |
| rs541923485 | snp | A/C | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4343977 | CCTGGCGCCGGGGTG[A/C]TGTCCATCTACTACC | 84954 |
| rs541932899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4358712 | CAAGCTCTTGAACCC[A/G]GGAGGTGGAGGTTAC | 84954 |
| rs542038408 | snp | G/T | 0.00159617 | 0.0282053 | downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4360289 | GGAGGGACCTCCTGG[G/T]GTGTGTGTGGCTTTG | 84954 |
| rs542094927 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4353966 | TGGGATTATAGGCAT[G/T]CACCACCACACCCAG | 84954 |
| rs542116897 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4341851 | AAACATGGTGAAACC[C/T]CTTCTCTACTAAAAA | 84954 |
| rs542512501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4356207 | ACCTCGCCAGCCCCC[C/T]CCCCTCTCAGAGCCT | 84954 |
| rs542715304 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4344839 | TGCCTCCCGGTTCAA[C/G]CGATTTTCTGCCTCA | 84954 |
| rs542757131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4350780 | AGTCTGGAGCCGGGC[A/G]AGGCTTGGGCTGGAG | 84954 |
| rs543214680 | in-del | -/GGC | 0.00358779 | 0.0422022 | cds-indel, nc-transcript-variant | MPND | GRCh38.p7 | 19:4343826 | GGCGGTGGACGCAGT[-/GGC]GGCGGCGGCGGCAGT | 84954 |
| rs543298301 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4359659 | GGAACCAGGCAGGGA[A/G]GGGCTGAAGTGGGGG | 84954 |
| rs543323650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4345403 | TGAATGGTAGCACAT[C/T]ATTCCCCTTCTGAAT | 84954 |
| rs543361212 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | MPND, SH3GL1 | GRCh38.p7 | 19:4359972 | TCACGTCCTGGAACA[A/G]GTGTGCGGCGTCCTC | 84954 |
| rs543512676 | snp | C/T | 0.000690687 | 0.0185706 | intron-variant, downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4359880 | GGCTGGCTAGGACCC[C/T]CGGGCACAGCCTGAG | 84954 |
| rs543534003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4349758 | TCAGGTGATCCGCCC[A/G]CCTCTGCCTCCCAAA | 84954 |
| rs543581951 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4351772 | GAGGCTGAGGCAGGA[A/G]AATCACTTGAACCCG | 84954 |
| rs543846518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4359527 | GCCCAGGGTCCTGGC[C/T]ACCCCTGAGTGTCTT | 84954 |
| rs543858723 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MPND | GRCh38.p7 | 19:4354790 | AATGGCTTGAACTGG[A/G]GAGGCGGAGGTTGCG | 84954 |
| rs543905551 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4347594 | AGTTTATTGCATGAA[C/G]GAGTTAACACTAGTC | 84954 |
| rs543959998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4352165 | GTGACAGAGTGAGAC[C/T]GTGTCTCAAAGAAAA | 84954 |
| rs544300345 | snp | C/T | | | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342522 | CCCACTTCCCGACTG[C/T]GGTCTGGGCAAAGCC | 84954 |
| rs544635854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4349067 | CTGGATAGTGGACAA[A/G]AGATATAATTCTGTT | 84954 |
| rs544716357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4346981 | GTTGCAGTGAGCTGA[A/G]ATCACACCACTGCAT | 84954 |
| rs544724761 | snp | C/G | 0.000990572 | 0.022233 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357406 | GGCTTCCAGCCCTGC[C/G]TCGCCCTGCTCTGCT | 84954 |
| rs544724829 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MPND | GRCh38.p7 | 19:4351690 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 84954 |
| rs544817490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4356042 | TATTTTTAGTTGAGA[C/T]AGGGTTTCACCATGT | 84954 |
| rs544945502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4351410 | GCCCGACTGGGAGGA[A/G]AGGTTACTGAAAGAC | 84954 |
| rs545542643 | in-del | -/T | 0.482234 | 0.0925596 | intron-variant | MPND | GRCh38.p7 | 19:4356636 | TGCCAGTTGCTATTC[-/T]TTTTTTTTTTTTCCT | 84954 |
| rs545557525 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342769 | TCCGCCCAAGGGTAT[A/G]GAGGGCCGGACTCGG | 84954 |
| rs545673067 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4355419 | CAGCTCCCTGCAAGC[C/T]CCGCCTCCCGGGTTC | 84954 |
| rs545892245 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4343130 | CCTGTGTCTGCGCGA[G/T]GCTGTTCCCTATTGG | 84954 |
| rs545911657 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | MPND | GRCh38.p7 | 19:4349377 | CACCGCAGCCAGTCA[C/G/T]GATTCCTTTGCCTTG | 84954 |
| rs546038967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4358631 | TGTCACTACCAAGAT[A/G]GAAAAGCTAGCCAGG | 84954 |
| rs546418135 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MPND | GRCh38.p7 | 19:4345687 | TGGGGAGGACCCCCC[A/G]GGAGAGAGGGCATGG | 84954 |
| rs546598050 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4355704 | TTGATCTCTTTACCT[C/T]GTGATCCGCCCACCT | 84954 |
| rs546606290 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4347690 | AGGACAGAAAGGAAA[G/T]TCTACTCATTGCAAG | 84954 |
| rs546801033 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | MPND | GRCh38.p7 | 19:4356801 | ACGCCACCACACCTG[C/G]CTAATTTTTGTATTT | 84954 |
| rs546893664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4352320 | TCCCATATGCTTAGC[A/G]TTCCAATAATGGAAC | 84954 |
| rs547112487 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4349979 | TGTATTCAGTTAGTG[A/G]CCAACTGTGTGCAAG | 84954 |
| rs547300432 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MPND | GRCh38.p7 | 19:4348538 | TGCTGAGATTATAGG[C/T]GTGAGCCATCGCGCC | 84954 |
| rs547490030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4359398 | GACCCTGGTCACCCC[A/G]TGGCCACCCCAGCAG | 84954 |
| rs547531993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4348582 | TTCTTAAACACCTTC[A/G]CTAGTTTCTTTTTAT | 84954 |
| rs547603167 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342915 | AAATCCGAGTTGGTG[A/T]AATCAGATAGTTGAC | 84954 |
| rs547998545 | in-del | -/CA | | | intron-variant | MPND | GRCh38.p7 | 19:4352209 | AGAATAGATAGAGTT[-/CA]GAGAGTTTAAACCCA | 84954 |
| rs548123040 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4344510 | TTCTGGTGGGGAGGA[C/T]GTAGATTACCAAACA | 84954 |
| rs548336782 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4357803 | CTCAGTACAAAGAGG[C/G]CTCCCTTCCTGACCC | 84954 |
| rs548488386 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342406 | CTGGGCTGGACAACA[A/G]TAGTTCACATGTACC | 84954 |
| rs548492683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4348996 | TCCTCAGTGCCAGCA[A/G]GAAGCAGGTCATCAC | 84954 |
| rs548548315 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4360176 | CCAGGGCAGGGCATT[A/C]ACTTCCAGGATACCC | 84954 |
| rs548553939 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4355836 | GTGCTGGGATTACAG[G/T]TGTGAGCCACTGCGC | 84954 |
| rs548610122 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4355492 | AGGTGCCTGCCACCA[C/G]GCCCAGCTAATTTTT | 84954 |
| rs548622412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4356069 | ATGTTGGCCAGGCTG[A/G]TTTCAAACTCCTGAC | 84954 |
| rs548680070 | snp | A/C | 2.35702e-05 | 0.00343286 | intron-variant | MPND | GRCh38.p7 | 19:4352853 | GAGCGGGGGGGCACC[A/C]AGCTGAGGGTCCCAC | 84954 |
| rs548822836 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4351020 | AGATGCTGCCGAGAA[C/G]GTGACGAGGACAGAA | 84954 |
| rs548995406 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4343346 | TCCCCATTCGCACCA[A/G]TGAGCTCCCGGTCAA | 84954 |
| rs549056868 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MPND | GRCh38.p7 | 19:4344350 | TCCCTTGCTTTAGGA[C/T]AAGCCCCAGTGTGGG | 84954 |
| rs549180788 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4349434 | GTGGCGGGAGAAGGC[A/G]AGTGGGAGGGATGGA | 84954 |
| rs549429449 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4354863 | AGCAAGACTGAGTCT[C/T]AAAGAGAATGAGGGC | 84954 |
| rs549563465 | snp | C/T | 0.00358779 | 0.0422022 | downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4360138 | GTGCCCAGGCTGGTA[C/T]CATCACCCCAGCTTC | 84954 |
| rs549607312 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4354265 | TGGGGGAGTCAGTGT[G/T]GGGGCGAGGGAAGAG | 84954 |
| rs549639802 | snp | C/T | 3.47614e-05 | 0.00416887 | intron-variant | MPND | GRCh38.p7 | 19:4359292 | ACCTCCTAACGGGGC[C/T]CCAGGAGAGGCCCCC | 84954 |
| rs549666925 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4349499 | CCGAGTCCTCAGTGG[C/T]TCAGTGAGTGGGTCT | 84954 |
| rs549787241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4359745 | GGGAGCCAGGCCCTC[A/G]GTTACATACTGCCCC | 84954 |
| rs549788618 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MPND | GRCh38.p7 | 19:4349126 | AGGCTGGAGTGCAGT[C/G]CTGTGATCTTGGCTC | 84954 |
| rs549821599 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4350470 | GGGTTAGGGTGGGAT[C/T]CAGGGACCAGGGCAG | 84954 |
| rs549891396 | snp | C/T | 5.0063e-05 | 0.0050029 | synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4359243 | GGAGCACACCTACCT[C/T]GACAAGCTTAAGGTG | 84954 |
| rs550002903 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4349563 | TTGCCCAGGCTGGAG[C/T]GCAATGGCGTGATCT | 84954 |
| rs550147373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4358471 | ATGAACACTTAAAAA[C/T]TGTGTGTTCAACATG | 84954 |
| rs550188637 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4346656 | TCCTGGCCTCCAGCA[A/G]TCCTCCCACCTGGAC | 84954 |
| rs550272930 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4343277 | GAGCCACTCGCGCAC[C/T]CGCCCCAGGCTTCCA | 84954 |
| rs550750414 | snp | C/T | | | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4341600 | GCATGCTGGTCACGC[C/T]TGTTGTCTCAGCTAC | 84954 |
| rs550864701 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4357160 | TCCCCAGGCCTGATA[C/G]ACAGCAGGAATTCGT | 84954 |
| rs551010503 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4351057 | ATGTGACCCAGAGAG[A/G]TCACCTCCACAAGGG | 84954 |
| rs551010772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4356621 | AAACACTACTCATAA[A/G]TGCCAGTTGCTATTC | 84954 |
| rs551070916 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4344394 | GGCCCAGAGCTCCTT[C/T]CCTGCAGGAGGAGCT | 84954 |
| rs551222068 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4350467 | CGGGGGTTAGGGTGG[G/T]ATCCAGGGACCAGGG | 84954 |
| rs551295972 | snp | A/G | 0.000250633 | 0.0111917 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4345832 | TCACCCAGCGCCTGG[A/G]CCACCCACTGCAAGA | 84954 |
| rs551400603 | in-del | -/C | 0.0103295 | 0.0711199 | intron-variant | MPND | GRCh38.p7 | 19:4359647 | CATGGGTGTCTGGAA[-/C]CCAGGCAGGGAGGGG | 84954 |
| rs551450015 | snp | C/T | | | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4341597 | CAGGCATGCTGGTCA[C/T]GCCTGTTGTCTCAGC | 84954 |
| rs551517367 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | MPND | GRCh38.p7 | 19:4344916 | TAATTTTTTTTTTTT[G/T]CAGTTTTAGTAGAGA | 84954 |
| rs551664402 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4359682 | AGTGGGGGCAGGATC[A/G]GGAGTGTGCACATAA | 84954 |
| rs552048325 | snp | A/G | 0.000198354 | 0.00995678 | intron-variant, missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4354971 | ACAGTCACCTGACAC[A/G]GAGTGAGGTCGTGGG | 84954 |
| rs552073469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4344481 | AGAGAGGAATCTGAG[A/G]CACAGATGGGTCCTT | 84954 |
| rs552139273 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4358931 | AGTGCAGGTCCAGGT[A/G]GACCTCTCGTGGCAG | 84954 |
| rs552277812 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4355956 | CCTTCCGGATTCAAG[C/T]GATTCTCCTGCCTCT | 84954 |
| rs552363289 | snp | A/G | 0.000148415 | 0.00861309 | intron-variant | MPND | GRCh38.p7 | 19:4357239 | TGCCCGCTGAGCTGC[A/G]CCTCTGTCCCCAGAT | 84954 |
| rs552449383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4352353 | TAGGCATAAATGGCA[A/G]TGGTGCTCACCAAAG | 84954 |
| rs552461635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4347823 | AGTCAGTCCAGTGTC[C/T]ACAAGGAACTGGCAA | 84954 |
| rs552522769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4348374 | CAAGCGATTCTCCTG[C/T]CTGAGCCTCTTGAGT | 84954 |
| rs552876409 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MPND | GRCh38.p7 | 19:4351260 | AGGTGTTCGCCACCA[C/T]GCCTGGCTAATTTTT | 84954 |
| rs553190190 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4346770 | GCACAGTGGCTCATG[C/T]CTGTAATCCCAGCAT | 84954 |
| rs553409441 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4347583 | TTTATGTACGAAGTT[C/T]ATTGCATGAAGGAGT | 84954 |
| rs553410069 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MPND | GRCh38.p7 | 19:4355849 | AGGTGTGAGCCACTG[C/T]GCCCGGCCTTTTTTT | 84954 |
| rs553473272 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4356319 | GCACTTAGGGAGGCC[A/G]AGGCAGGAGGTTTGC | 84954 |
| rs553733030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4352468 | GGTGGGTGGATCACC[C/T]GAGGTCGGGAGTTTG | 84954 |
| rs553801180 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4358548 | ATCCCAGCACTTTGG[A/G]AGGCTGAGGTGGGTG | 84954 |
| rs553813743 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4359008 | ACCTAAGCTAGGTGA[C/G]CCCTCTGGCTAAGGT | 84954 |
| rs554014441 | snp | A/G | 0.002331 | 0.0340597 | intron-variant, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357962 | CCAGGTGCCGATCCC[A/G]GTGCAGAGCTGAGCC | 84954 |
| rs554018290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4352072 | CAGCTACTCAGGAGG[C/T]TGAGGCAAGAGAATG | 84954 |
| rs554205081 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4341647 | AGAGGATCATTTGAG[C/T]CCAGGAGGCCAAGGC | 84954 |
| rs554464942 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4352474 | TGGATCACCTGAGGT[C/T]GGGAGTTTGAGACCA | 84954 |
| rs554671891 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4358510 | ACACTAAACTAAGGC[A/C]GACATAGTGGCTCAC | 84954 |
| rs554690816 | in-del | -/AAAAAAAAAAAA | | | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342043 | AAAAAAAAAAAAAAA[-/AAAAAAAAAAAA]GAAAAAAGAAAAGAA | 84954 |
| rs554792392 | snp | A/C | | | intron-variant | MPND | GRCh38.p7 | 19:4352696 | CTCAAAAATAAATAA[A/C]TAAAAAATAAATTAC | 84954 |
| rs554929638 | snp | C/T | 0.00013671 | 0.00826658 | missense, intron-variant, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357323 | ACCCACACAGCCCGG[C/T]GCTGCCATCTCTGCA | 84954 |
| rs554931002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4356946 | CTCCCAGCCTAGTTT[C/T]AACTGTTTGTTGAGT | 84954 |
| rs555051709 | snp | C/T | 0.0013317 | 0.0257697 | intron-variant, missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4355103 | TCCCCACAGTGCTGA[C/T]GGTGCTCAGAGCCTT | 84954 |
| rs555054811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4347529 | CAAGTGTGAGCCACC[A/G]CGCCCAGCTGCCTGT | 84954 |
| rs555151255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4359467 | CTCCGGCAGTGCCGG[A/G]TGAGGTCCTGGCAGC | 84954 |
| rs555214605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4359812 | CCCTGTGCCTCGGTC[C/T]CAGGGGGGCTCAGTC | 84954 |
| rs555459285 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MPND | GRCh38.p7 | 19:4344691 | AAAGCCCTCAGCAGG[C/T]GCCTGCCACATGGTA | 84954 |
| rs555520199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4345194 | TGGGATTACAGGCAC[C/T]CGCCACCACGCCTGG | 84954 |
| rs555610539 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342621 | TGCCAGGGACTGAGG[A/G]AAATCCCAGAGCCTG | 84954 |
| rs555725149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4353634 | TGGTGCAATCATGGC[C/T]AACTGCAGCCTCAAC | 84954 |
| rs555739714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4349214 | CTGGGACTACAAGGG[C/T]GCGCCACCAAGCTCA | 84954 |
| rs555970469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4348914 | CCTGCCTCAGCCTCC[C/T]AAAGTGCTGGGATTA | 84954 |
| rs556234560 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MPND | GRCh38.p7 | 19:4349396 | TCCTTTGCCTTGGTG[A/G]GAACTGCCTGTGGAA | 84954 |
| rs556308252 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4343665 | CGCGGGGCTGCAGAG[C/G]CGTGGGGCGAGCGGC | 84954 |
| rs556452238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4348813 | AGGCGCCCACCACCA[A/G]GCCTGGCTAATTTTT | 84954 |
| rs556570344 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342539 | GTCTGGGCAAAGCCA[A/C]CCGCACTTGAGCCCA | 84954 |
| rs556642271 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | MPND | GRCh38.p7 | 19:4348234 | TACAGTATCATTGCA[A/G]GCAGGCAAATTGCAA | 84954 |
| rs556695113 | snp | A/G | 0.000337211 | 0.0129804 | intron-variant, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357980 | GCAGAGCTGAGCCGG[A/G]GTGTGCACTCTCCCG | 84954 |
| rs556780240 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MPND | GRCh38.p7 | 19:4350745 | CCCACATGGAGACAT[A/G]GAGAGGCAGCTGGGC | 84954 |
| rs556857804 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4355779 | TGGTCAGGATGGTCT[C/T]GATCTCTTGACCTCG | 84954 |
| rs557158249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4356281 | TCAGATCCAGGCACC[A/G]GGGGTTCACACCTGG | 84954 |
| rs557249913 | snp | C/G | | | intron-variant | MPND | GRCh38.p7 | 19:4359471 | GGCAGTGCCGGATGA[C/G]GTCCTGGCAGCGGGT | 84954 |
| rs557318044 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4350618 | AGATCAGATGCTGGA[G/T]TCCTGAGCAAGTGGG | 84954 |
| rs557517316 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | MPND | GRCh38.p7 | 19:4345349 | ACTGCACCCAGCCCT[G/T]TATTATTACTATTAC | 84954 |
| rs557614032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4344599 | AGATGGGCAACACCC[C/T]GGCCTTCCTGTGGTT | 84954 |
| rs557665890 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4359833 | GGGCTCAGTCAGGAT[G/T]CTGGACTTGCACGGT | 84954 |
| rs557721750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4344793 | GCCCAGGCTGGAATG[C/T]AGTTGCTCGATCTCG | 84954 |
| rs557783765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4359673 | AGGGGCTGAAGTGGG[A/G]GCAGGATCGGGAGTG | 84954 |
| rs558128240 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MPND | GRCh38.p7 | 19:4343642 | CGCGGGGCGCGGGGC[C/T]GCAGGGGCGCGGGGC | 84954 |
| rs558315054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4349296 | GGTCAGGCTGGTCTC[A/G]AACTCCTGACCTCAA | 84954 |
| rs558377064 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4343069 | GCCCGGGAGGGTGGG[A/T]GTTAATTCTTTAGCG | 84954 |
| rs558459127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4346901 | CAGGCGTGGTGGTGC[A/G]CGCCTGTAGTCCCAG | 84954 |
| rs558838889 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4347461 | AGCCAGGATGATCTC[G/T]ATCTCCTGACCTCGT | 84954 |
| rs558928346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4352161 | CTGGGTGACAGAGTG[A/G]GACCGTGTCTCAAAG | 84954 |
| rs558988768 | snp | C/G | | | intron-variant | MPND | GRCh38.p7 | 19:4351083 | AAGGGCAGTTTAGGA[C/G]AGAACTGGAGGAGAG | 84954 |
| rs559044517 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MPND | GRCh38.p7 | 19:4351653 | AAATCACAAGGTCAG[A/G]CGATCGAGACCATCC | 84954 |
| rs559189313 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4353098 | GGAGGAGACTGGGGA[A/G]AGGTTGGGCCTTGAT | 84954 |
| rs559483581 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4345633 | CCTGAGAGGTGTTCC[G/T]GGAAGCCCTGTAAAG | 84954 |
| rs559496760 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4350348 | ACTTGGGCTTTGACC[A/G]GGAGGAAGGTGGGAG | 84954 |
| rs559769211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4350857 | AGAGGGGATGAGGCC[A/G]CCTGGGAGGGGTGTG | 84954 |
| rs559778859 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4355334 | AAGGGTGAAGAACAC[C/T]GCTTTTTTTTTTTTT | 84954 |
| rs559964613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4348935 | GCTGGGATTATAGGC[A/G]TGAGCCACCATGCCC | 84954 |
| rs559993462 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4357887 | GTCATTTCAGGGCCC[C/T]GGCTCTCCTCTGGGC | 84954 |
| rs560013841 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MPND | GRCh38.p7 | 19:4359670 | GGGAGGGGCTGAAGT[G/T]GGGGCAGGATCGGGA | 84954 |
| rs560027818 | snp | C/G | | | intron-variant | MPND | GRCh38.p7 | 19:4355220 | GGAGGGTTGGGAAGG[C/G]ACATAGCTGTCCTGG | 84954 |
| rs560126021 | snp | C/G | 0.000399281 | 0.0141238 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | MPND, SH3GL1 | GRCh38.p7 | 19:4359975 | CGTCCTGGAACAGGT[C/G]TGCGGCGTCCTCAAG | 84954 |
| rs560144494 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342242 | GTGGCTCAGGGTTTT[A/G]GAAGGCAGGGGACGG | 84954 |
| rs560188971 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4352840 | GGGATTTAGCAGGGA[C/G]CGGGGGGGCACCCAG | 84954 |
| rs560411336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4357691 | ACTGGAGAGTTGGGG[C/T]CCCAGTTTCTCCATC | 84954 |
| rs560474189 | snp | C/T | 0.000381243 | 0.0138013 | intron-variant | MPND | GRCh38.p7 | 19:4358190 | GAGCTCGCTGCGGGG[C/T]GGGCAGGCAGGGGCT | 84954 |
| rs560517035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4351459 | TGGTGCTGGCTCGCT[C/T]AATGAACGGAGCATC | 84954 |
| rs560531512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4346521 | CTCCTGGGTTCAAGC[A/G]ATCCTCCCACCTCAG | 84954 |
| rs560538872 | snp | C/G | | | intron-variant | MPND | GRCh38.p7 | 19:4349205 | CCAGAGTAGCTGGGA[C/G]TACAAGGGCGCGCCA | 84954 |
| rs560600783 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4350224 | GTGTTGGAGGAACAG[C/T]GAGGAGCCTGTGTGG | 84954 |
| rs560618230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4347638 | GACCACAAATGGTTA[C/T]GTTATACAAGCTGTG | 84954 |
| rs560747554 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4351678 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCATCT | 84954 |
| rs560792197 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4352729 | ATAAATAAAAAAAAA[A/T]GTGAGGTCTTAGCTT | 84954 |
| rs560936739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4357663 | TAGGCAGGGGCCCCT[A/G]GTTCCAGGCTCCACT | 84954 |
| rs561309276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4347020 | GGCAACAGATTGAGA[C/T]TCCATTTCAAAACAA | 84954 |
| rs561595066 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4351413 | CGACTGGGAGGAAAG[G/T]TTACTGAAAGACGTG | 84954 |
| rs561650773 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4343228 | CAAGTGCGGTGACCG[C/T]AGGTCTCACCTTCTC | 84954 |
| rs561711009 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4344087 | GGACAAGCTTCAGTG[C/T]AGGGAGGGGACACTG | 84954 |
| rs561740113 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4353986 | ACCACACCCAGTGGC[C/T]ACCTAATTTGTTCTA | 84954 |
| rs561914936 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4353360 | GCAACCTCTGCCTCC[C/T]GGGTTCAAGCGATTC | 84954 |
| rs561929247 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4349055 | AGAGTGGAGGTTCTG[C/G]ATAGTGGACAAAAGA | 84954 |
| rs562344830 | in-del | -/TTT | | | intron-variant | MPND | GRCh38.p7 | 19:4355335 | GGGTGAAGAACACTG[-/TTT]CTTTTTTTTTTTTTT | 84954 |
| rs562388003 | snp | C/G | | | intron-variant | MPND | GRCh38.p7 | 19:4356611 | CTCATCTATTAAACA[C/G]TACTCATAAGTGCCA | 84954 |
| rs562407902 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342611 | CTTTCAACCCTGCCA[A/G]GGACTGAGGGAAATC | 84954 |
| rs562521481 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4343156 | ATTGGAGTCCGCATT[A/G]TTCCCCTGGACCTGA | 84954 |
| rs562537505 | snp | A/C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342835 | CCAGTCCCTGCCTCT[A/C/G]ATGGTTTGCGCTCAT | 84954 |
| rs562664946 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime, downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4360487 | ATGTACTTCTGACGA[-/G]GGGGGTGCAGGGCAG | 84954 |
| rs562696441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4358232 | GCTGGGCACACGATG[C/T]GTTGGTCTGCTTCCC | 84954 |
| rs562719540 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | MPND | GRCh38.p7 | 19:4352145 | GCCACTGCGCTCCAG[A/C]CTGGGTGACAGAGTG | 84954 |
| rs562738862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4348421 | ACACACCACCACACC[C/T]GGCTAATTTTTGTAT | 84954 |
| rs562781546 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4347585 | TATGTACGAAGTTTA[C/T]TGCATGAAGGAGTTA | 84954 |
| rs562966192 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4360158 | ACCCCAGCTTCCTCA[C/T]TTCCAGGGCAGGGCA | 84954 |
| rs563034180 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4346617 | AGATGAGGTTTCACC[A/G]TGTTGCCTAGGCTGG | 84954 |
| rs563121351 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4350265 | GTGAGTAAGGGAGAG[A/G]GAAGGAGGTGGGGAG | 84954 |
| rs563184758 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MPND | GRCh38.p7 | 19:4344804 | AATGCAGTTGCTCGA[C/T]CTCGGCTCACTGCAA | 84954 |
| rs563410117 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MPND | GRCh38.p7 | 19:4349790 | TGCTGGGATTGCAGG[C/T]GTGAGCCAGCCATGG | 84954 |
| rs563691840 | snp | C/T | 1.74708e-05 | 0.00295552 | intron-variant | MPND | GRCh38.p7 | 19:4354142 | CAGGTCAGACTCACC[C/T]CAAGTTCTGCCCCTG | 84954 |
| rs563771474 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4355234 | GGACATAGCTGTCCT[C/G]GCGACTGCCCAGTGG | 84954 |
| rs563938304 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4354736 | GGGCATGGTGGTGCA[C/T]GCCTCTAATCCCAGC | 84954 |
| rs563950786 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4349738 | CTAGTCTTGAACTCC[G/T]GACCTCAGGTGATCC | 84954 |
| rs564038440 | snp | A/G | 0.000385987 | 0.0138868 | intron-variant | MPND | GRCh38.p7 | 19:4359258 | CGACAAGCTTAAGGT[A/G]AGCCCCAAGTCCCCG | 84954 |
| rs564046940 | snp | G/T | | | downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4360358 | CCCCTGCACCAAGAC[G/T]AGGCAAGGGGCTGTA | 84954 |
| rs564129115 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4358783 | CAGAGTGAGACCCTA[C/G]CTCAAGGAAAAAACC | 84954 |
| rs564199724 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MPND | GRCh38.p7 | 19:4344159 | CGAGGGGAAACTGAG[A/G]CCCGGGGCTCCGTTG | 84954 |
| rs564283246 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4349452 | TGGGAGGGATGGAGC[G/T]TCAGGAAGTGAGGGT | 84954 |
| rs564511063 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342691 | AGTTGCAGAAACAGG[A/G]TAGGGGACAAAGGCC | 84954 |
| rs564720150 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4356644 | TGCTATTCTTTTTTT[G/T]TTTTCCTTTTCTTTG | 84954 |
| rs564899029 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MPND | GRCh38.p7 | 19:4357126 | GGTGGGGGCAGGGCC[C/T]GTCTTGGTCATCACT | 84954 |
| rs564957016 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4359706 | CACATAAGCCCCACC[C/T]CTCCACACAGCACCG | 84954 |
| rs565326778 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | MPND, SH3GL1 | GRCh38.p7 | 19:4360066 | CTCAGGTAATAAAGA[A/T]ACGGAAGCAGCAGCC | 84954 |
| rs565415965 | snp | A/C | | | intron-variant | MPND | GRCh38.p7 | 19:4349984 | TCAGTTAGTGGCCAA[A/C]TGTGTGCAAGGCCTG | 84954 |
| rs565544049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4356002 | AGGATTACAGGTGTG[C/T]GCCACCATCTCCAGC | 84954 |
| rs565553793 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4359816 | GTGCCTCGGTCTCAG[G/T]GGGGCTCAGTCAGGA | 84954 |
| rs565563032 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4350561 | GGAAGAAGTGGGCAG[A/G/T]TTCCAGGTATTTTTG | 84954 |
| rs565674106 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4345254 | GTTTCACCATGTTGG[A/C]CAGGCTGGTCTCAAA | 84954 |
| rs565684556 | snp | A/C | 0.000798403 | 0.0199641 | downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4360225 | GAACTGGCACAAAAG[A/C]CTCAGGGCCAGTCCC | 84954 |
| rs565733924 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | MPND | GRCh38.p7 | 19:4343570 | AGCCGGAGTCTAGAG[C/T]TCCGGGCGCGGGGAG | 84954 |
| rs566223853 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4353637 | TGCAATCATGGCTAA[C/T]TGCAGCCTCAACCTC | 84954 |
| rs566472525 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | MPND | GRCh38.p7 | 19:4357169 | CTGATACACAGCAGG[-/A]ATTCGTTCAGGGCTG | 84954 |
| rs566674406 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | MPND | GRCh38.p7 | 19:4351892 | AAAAGAATAGAGTTG[G/T]CTGGGCACGGTGGCT | 84954 |
| rs566721676 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MPND | GRCh38.p7 | 19:4347366 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 84954 |
| rs566999289 | snp | A/G | 0.000798881 | 0.01997 | intron-variant | MPND | GRCh38.p7 | 19:4356827 | TATTTTTAGTAGAGA[A/G]GGGGGTTTCTCCATG | 84954 |
| rs567052308 | snp | C/T | 0.00178455 | 0.0298177 | intron-variant | MPND | GRCh38.p7 | 19:4345998 | TACGTGCTGCAGCCT[C/T]CTCCAGGAAGCCGCC | 84954 |
| rs567144765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4351818 | AGTGAGCCGAGATCA[C/T]GCCACTGCACTCCAG | 84954 |
| rs567181400 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | MPND | GRCh38.p7 | 19:4352466 | GAGGTGGGTGGATCA[-/C]CTGAGGTCGGGAGTT | 84954 |
| rs567370375 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4351189 | GTTCACTGCAGTCTC[C/T]GCCTCCCGGGTTCAA | 84954 |
| rs567584986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4351581 | AAGAATAGACTTGGC[A/G]GCCGGGCACGGTGGC | 84954 |
| rs567842721 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4350482 | GATCCAGGGACCAGG[A/G/T]CAGAGGTGAGTGAGC | 84954 |
| rs567916769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4344894 | GGTATGCGCCACCAC[A/G]CCTGGCTAATTTTTT | 84954 |
| rs568136235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4358280 | GCTATGGCTGGTGGC[A/G]CCTTGGGGGCCTGGG | 84954 |
| rs568208588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4358926 | CGGTGAGTGCAGGTC[C/T]AGGTGGACCTCTCGT | 84954 |
| rs568258714 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4359338 | GTGGCAGCAATGAGC[C/T]CCGTGGGCCTCAGGG | 84954 |
| rs568277951 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342444 | TGCTCTATGTCAAGT[C/T]TTCTTCCTGAGAACA | 84954 |
| rs568493740 | snp | C/T | 0.00111221 | 0.0235556 | intron-variant | MPND | GRCh38.p7 | 19:4352876 | GGTCCCACCGCTGTC[C/T]CTGACCCCTAACCCC | 84954 |
| rs568576159 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4348007 | AATGATTCTCCTGCC[A/T]CAGTCTCGCGAGTAG | 84954 |
| rs569065801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4347475 | CGATCTCCTGACCTC[A/G]TGATCCACCCACCTC | 84954 |
| rs569077946 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4347846 | ACTGGCAAATGTTCT[C/T]GCACTGGTCACTCTG | 84954 |
| rs569249456 | snp | C/G/T | 3.54266e-05 | 0.0042086 | missense, intron-variant, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357274 | CAGAGCCTGTTCCTG[C/G/T]GGGGCCTGTCCCTGG | 84954 |
| rs569281508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4357749 | TGCCCATATTTTGGT[A/G]AGGTCCTGGGCGTGG | 84954 |
| rs569509405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4359786 | CAGCAGGCTGTGCTG[C/T]GGGACCCCAGCCCTG | 84954 |
| rs569720232 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342974 | GCTTGCTATCGATTG[C/G]TTGAGGGTGAAATAA | 84954 |
| rs569765518 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4355480 | AGCTGGGACTACAGG[C/T]GCCTGCCACCACGCC | 84954 |
| rs569979331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4359456 | GGAGCTTTAAGCTCC[A/G]GCAGTGCCGGATGAG | 84954 |
| rs569990917 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4351253 | GGATTGCAGGTGTTC[A/G]CCACCATGCCTGGCT | 84954 |
| rs570043210 | snp | A/T | | | intron-variant | MPND | GRCh38.p7 | 19:4355847 | ACAGGTGTGAGCCAC[A/T]GCGCCCGGCCTTTTT | 84954 |
| rs570171159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4358875 | GGCCGAACCAGGGGG[C/T]CACGTCAGGCCCGCG | 84954 |
| rs570190898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4358486 | TTGTGTGTTCAACAT[A/G]CATTTAAAACACTAA | 84954 |
| rs570515123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4353512 | ACCTCAGGTGATCCA[C/T]CTGCCTCGGCCTCCC | 84954 |
| rs570529993 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342921 | GAGTTGGTGTAATCA[C/G]ATAGTTGACACGGAT | 84954 |
| rs570551986 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4359720 | CCCTCCACACAGCAC[C/T]GCTGCCCCTGGGAGC | 84954 |
| rs570609323 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4345528 | CTTGGTCATGGTGGG[C/T]GGGGTGCAGATATCT | 84954 |
| rs570647282 | snp | A/G/T | | | intron-variant | MPND | GRCh38.p7 | 19:4348422 | CACACCACCACACCC[A/G/T]GCTAATTTTTGTATT | 84954 |
| rs570655706 | snp | A/C | | | intron-variant | MPND | GRCh38.p7 | 19:4358944 | GTGGACCTCTCGTGG[A/C]AGCCACTTGGGCAAC | 84954 |
| rs570723586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357966 | GTGCCGATCCCGGTG[C/T]AGAGCTGAGCCGGGG | 84954 |
| rs570835909 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4358328 | ACTCAGGACAGAGTC[C/G]AGGCCCTTGCCAGGG | 84954 |
| rs570902410 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MPND | GRCh38.p7 | 19:4351103 | CTGGAGGAGAGGTTA[C/T]TTTTAATTTGTATTT | 84954 |
| rs570976044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4346577 | GCATGCCACCACACC[C/T]GGCTAATTTTTGGAT | 84954 |
| rs571158578 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4346047 | GGGGTGCCCAGCCTG[C/G]CACAGCTCTCTCCGG | 84954 |
| rs571310150 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4360275 | GCACCTGGGGTGCTG[A/G]AGGGACCTCCTGGGG | 84954 |
| rs571773414 | snp | C/G | | | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4343092 | CTTTAGCGACTGAGG[C/G]CGGCTTGGGCTCTTT | 84954 |
| rs571812230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4344494 | AGGCACAGATGGGTC[C/T]TTCTGGTGGGGAGGA | 84954 |
| rs571862952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4359477 | GCCGGATGAGGTCCT[A/G]GCAGCGGGTTTTGGG | 84954 |
| rs571871742 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4350092 | AGGTGGTTGGGGGGG[C/T]TTCACTGAGAAGGTG | 84954 |
| rs571878151 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4353624 | CAGAGTACAGTGGTG[C/T]AATCATGGCTAACTG | 84954 |
| rs571968437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4350187 | GCCTCTGCAAAGGCC[C/T]TGGGGCACGACCGTG | 84954 |
| rs572035450 | snp | A/G | 6.74548e-05 | 0.00580714 | intron-variant, synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4355104 | CCCCACAGTGCTGAC[A/G]GTGCTCAGAGCCTTC | 84954 |
| rs572306570 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342673 | GGACAGGGTCGGGGA[G/T]GTAGTTGCAGAAACA | 84954 |
| rs572395181 | in-del | -/AA | 0.0115144 | 0.0749975 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342056 | AAAAAAAAAAAAAAG[-/AA]AAAAGAAAAGAAAAG | 84954 |
| rs572441110 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4343062 | GAGGGCCGCCCGGGA[G/T]GGTGGGAGTTAATTC | 84954 |
| rs572509294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4348929 | CAAAGTGCTGGGATT[A/G]TAGGCGTGAGCCACC | 84954 |
| rs572558688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4350225 | TGTTGGAGGAACAGC[A/G]AGGAGCCTGTGTGGC | 84954 |
| rs572625055 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4349260 | TTTGCATGTTTATTA[G/T]AGATGCGGTTTCACC | 84954 |
| rs572644353 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4357052 | GTGGCAGGGTGCATC[A/T]TTTATATTAAAAGAG | 84954 |
| rs572829968 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4359774 | CCACTGGGTAAGCAG[C/T]AGGCTGTGCTGCGGG | 84954 |
| rs573115249 | snp | C/G | | | intron-variant | MPND | GRCh38.p7 | 19:4347711 | TCATTGCAAGGAAAT[C/G]CTCACTTAAGCTTCA | 84954 |
| rs573153044 | snp | A/G | | | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4341968 | GGCAGAGGTTGTAGC[A/G]AGCCAAGATCTTGCC | 84954 |
| rs573172196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4350873 | CCTGGGAGGGGTGTG[A/G]AGGGAGGAGGCCTGA | 84954 |
| rs573289738 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4356372 | GCCACAGCAAGACCC[C/T]GTCTCTACAAAAGAT | 84954 |
| rs573311954 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MPND | GRCh38.p7 | 19:4351377 | CAAAGTGCTGGGATT[A/G]CAGGCGTGGGCCACT | 84954 |
| rs573501364 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4357771 | TGGGCGTGGGGCCTC[C/T]GTTGTGTCATTGGCT | 84954 |
| rs573554855 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4356141 | ACAGGTGTGAGCCAC[C/T]GCGCCCAGCCTAAGA | 84954 |
| rs573617627 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4360356 | CACCCCTGCACCAAG[A/G]CGAGGCAAGGGGCTG | 84954 |
| rs574036363 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | MPND | GRCh38.p7 | 19:4359101 | ACTGGAACCCCAGGA[A/G]AGGCGCTGAGGTACC | 84954 |
| rs574037276 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MPND | GRCh38.p7 | 19:4355236 | ACATAGCTGTCCTGG[C/T]GACTGCCCAGTGGCT | 84954 |
| rs574056829 | snp | A/G | 0.00023547 | 0.010848 | missense, downstream-variant-500B, nc-transcript-variant | MPND, SH3GL1 | GRCh38.p7 | 19:4359961 | CAGAGCCTGTGTCAC[A/G]TCCTGGAACAGGTGT | 84954 |
| rs574126755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4355834 | AAGTGCTGGGATTAC[A/G]GGTGTGAGCCACTGC | 84954 |
| rs574324937 | in-del | -/G | 0.00993419 | 0.0697739 | intron-variant | MPND | GRCh38.p7 | 19:4350085 | GGGAAGAAGGTGGTT[-/G]GGGGGGCTTCACTGA | 84954 |
| rs574440881 | snp | C/G | | | intron-variant | MPND | GRCh38.p7 | 19:4351658 | ACAAGGTCAGACGAT[C/G]GAGACCATCCTGGCT | 84954 |
| rs574496466 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4353102 | GAGACTGGGGAGAGG[C/T]TGGGCCTTGATCTTC | 84954 |
| rs574568444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4358514 | TAAACTAAGGCAGAC[A/G]TAGTGGCTCACGCCT | 84954 |
| rs574702454 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MPND | GRCh38.p7 | 19:4352047 | GCATGGTGGTGGGCA[A/G]CTGTACTCCCAGCTA | 84954 |
| rs574906886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4356540 | ACAGAGCAAGACCCT[A/G]TATCTAAGAACATAA | 84954 |
| rs575001198 | snp | A/G | | | downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4360251 | GTCCCACCCACCTTG[A/G]GCTCAGGAGCACCTG | 84954 |
| rs575087917 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4355374 | GGAGTCTCGCTCTGT[C/T]ACCCAGGCTAGAGTG | 84954 |
| rs575292066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357994 | GGGTGTGCACTCTCC[C/T]GTTCCCAGCCCGGGC | 84954 |
| rs575433848 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | MPND | GRCh38.p7 | 19:4359512 | GCTCCCCTGCAGAGG[G/T]CCCAGGGTCCTGGCC | 84954 |
| rs575667492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4351394 | AGGCGTGGGCCACTG[C/T]GCCCGACTGGGAGGA | 84954 |
| rs575726233 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | MPND | GRCh38.p7 | 19:4351654 | AATCACAAGGTCAGA[A/C]GATCGAGACCATCCT | 84954 |
| rs575728277 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4346377 | TTCCCTGAGTGTTCA[C/T]CAGCCGGGTGAACTT | 84954 |
| rs575938556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4356415 | CCAGACATGGTGGTA[C/T]GCACCTGTAGTCCCA | 84954 |
| rs575950360 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | MPND | GRCh38.p7 | 19:4354579 | AATGTATGAAGGAGG[G/T]TGCGTGGCCAGGCCC | 84954 |
| rs576159840 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4358711 | ACAAGCTCTTGAACC[C/T]GGGAGGTGGAGGTTA | 84954 |
| rs576360006 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4348857 | AGACGGGGTTTCACC[A/G]TTTTGGCCAGGCTGG | 84954 |
| rs576375664 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4348708 | TGTCGCCCAGGCTGG[A/T]ATGCAGTGGTGCAAT | 84954 |
| rs576517400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4352662 | GCACTCCAGACTGGG[C/T]GACAGAGAGAGACTC | 84954 |
| rs576644618 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4354754 | CTCTAATCCCAGCTA[C/T]CTGAGAGGCTGAGAC | 84954 |
| rs576715747 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4341821 | CTGAGGTTGGGAGTT[C/T]GAGACCAGCCTGGCA | 84954 |
| rs576864596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4353191 | GACGAGGCCTGGGCT[A/G]AAGACAGTCCCACTG | 84954 |
| rs576930801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4348950 | GTGAGCCACCATGCC[C/T]GGCCTCTGTTGAATT | 84954 |
| rs576975946 | snp | C/T | 1.75548e-05 | 0.00296262 | synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357384 | GCGGCTGCAGGGCTC[C/T]AGCAATGGCTTCCAG | 84954 |
| rs577042479 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4349319 | GACCTCAAGTGATCC[A/T]CTCGCTTCGGTATCC | 84954 |
| rs577433622 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4350206 | GGCACGACCGTGCCT[C/G]GTGTGTTGGAGGAAC | 84954 |
| rs577544512 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4350623 | AGATGCTGGAGTCCT[C/G]AGCAAGTGGGTGGAT | 84954 |
| rs577646614 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MPND | GRCh38.p7 | 19:4345569 | TTGGTGCAGGCTGAT[C/T]AGGTTTGTGGGTGTG | 84954 |
| rs577757890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4354737 | GGCATGGTGGTGCAC[A/G]CCTCTAATCCCAGCT | 84954 |
| rs577785066 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MPND | GRCh38.p7 | 19:4351386 | GGGATTGCAGGCGTG[A/G]GCCACTGTGCCCGAC | 84954 |
| rs577888956 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | MPND | GRCh38.p7 | 19:4344799 | GCTGGAATGCAGTTG[C/T]TCGATCTCGGCTCAC | 84954 |
| rs578079798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4359845 | GATGCTGGACTTGCA[C/T]GGTGGACTGTGAGGC | 84954 |
| rs578125855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MPND | GRCh38.p7 | 19:4343659 | CAGGGGCGCGGGGCT[A/G]CAGAGCCGTGGGGCG | 84954 |
| rs745359280 | snp | A/C | | | intron-variant | MPND | GRCh38.p7 | 19:4356765 | TGCCTCAGCCTCCAT[A/C]GTAGATGGGAGTACA | 84954 |
| rs745419545 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4347701 | GAAATTCTACTCATT[A/G]CAAGGAAATCCTCAC | 84954 |
| rs745441665 | snp | G/T | 1.69789e-05 | 0.00291362 | intron-variant | MPND | GRCh38.p7 | 19:4355074 | GACCGGGGTCACGGG[G/T]TCACAGCTGCCCCTC | 84954 |
| rs745478748 | snp | G/T | 3.47881e-05 | 0.00417047 | intron-variant | MPND | GRCh38.p7 | 19:4355047 | AGGGCCAGGTGGGCG[G/T]GGGCGTTGGAGGACC | 84954 |
| rs745500688 | snp | C/T | 9.37163e-05 | 0.00684466 | synonymous-codon, intron-variant, nc-transcript-variant | MPND | GRCh38.p7 | 19:4358097 | GCAAAGGCCCAGTGA[C/T]TATGGCATCCCCATG | 84954 |
| rs745744242 | snp | A/G | 0.000123498 | 0.00785708 | intron-variant | MPND | GRCh38.p7 | 19:4345986 | CTGCTGATGAGGTAC[A/G]TGCTGCAGCCTCCTC | 84954 |
| rs745778307 | snp | A/C | | | intron-variant | MPND | GRCh38.p7 | 19:4348931 | AAGTGCTGGGATTAT[A/C]GGCGTGAGCCACCAT | 84954 |
| rs745780665 | in-del | -/A | 2.23018e-05 | 0.00333922 | intron-variant | MPND | GRCh38.p7 | 19:4352882 | CCGCTGTCCCTGACC[-/A]CCTAACCCCTGCAGA | 84954 |
| rs745832290 | snp | C/T | 1.68337e-05 | 0.00290114 | synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4345900 | GGCCTCTGTCAAGTA[C/T]AAAGGCCAGAAACTG | 84954 |
| rs745876266 | snp | C/T | 0.000347001 | 0.0131674 | intron-variant, downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4359881 | GCTGGCTAGGACCCC[C/T]GGGCACAGCCTGAGG | 84954 |
| rs746035864 | snp | A/G | 0.000179003 | 0.00945883 | synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4343880 | CGGCGGGGCCGGGGC[A/G]GGGGGCTGCGGCGGG | 84954 |
| rs746039807 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4348149 | CGCCCGCCTCCGCCT[C/T]CCAAAATGCTGGGAT | 84954 |
| rs746052487 | snp | G/T | | | intron-variant | MPND | GRCh38.p7 | 19:4352822 | AGGCCAAAGGGCTGG[G/T]GTGGGATTTAGCAGG | 84954 |
| rs746085670 | snp | A/G | 1.66932e-05 | 0.002889 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4359245 | AGCACACCTACCTCG[A/G]CAAGCTTAAGGTGAG | 84954 |
| rs746232506 | snp | A/C | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4360484 | CTCATGTACTTCTGA[A/C]GAGGGGGGTGCAGGG | 84954 |
| rs746276763 | snp | C/T | 5.01626e-05 | 0.00500787 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4354065 | ACAACCCCAGGGAAG[C/T]GGGTGGACAGCAAGA | 84954 |
| rs746289693 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4350230 | GAGGAACAGCGAGGA[A/G]CCTGTGTGGCTGGAG | 84954 |
| rs746311066 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4357819 | CTCCCTTCCTGACCC[C/T]GCCTGGCTTCATTCC | 84954 |
| rs746407664 | snp | C/T | 5.12983e-05 | 0.00506424 | missense, intron-variant, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357320 | GCCACCCACACAGCC[C/T]GGCGCTGCCATCTCT | 84954 |
| rs746594531 | snp | A/G | | | upstream-variant-2KB | MPND | GRCh38.p7 | 19:4342213 | CCAGGATTTGGGTGC[A/G]AGAGGCTGGAGGTGT | 84954 |
| rs746614345 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4359121 | GCTGAGGTACCTCAG[A/G]CTTGGAGGGAGCCTG | 84954 |
| rs746623209 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4358240 | CACGATGCGTTGGTC[C/T]GCTTCCCACCGGTGG | 84954 |
| rs746629862 | snp | A/C | 3.4075e-05 | 0.00412751 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4345920 | GCCAGAAACTGGACA[A/C]GTACAAGGCCACCTG | 84954 |
| rs746646152 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4349011 | GGAAGCAGGTCATCA[C/T]TGTTACTTGCATCAG | 84954 |
| rs746690688 | snp | A/C/T | 3.33802e-05 | 0.00408524 | intron-variant | MPND | GRCh38.p7 | 19:4359149 | CTGGGAGTCCATGCT[A/C/T]CTCTGTCCTGTAGAT | 84954 |
| rs746692889 | snp | A/G | 1.65326e-05 | 0.00287507 | intron-variant, splice-acceptor-variant | MPND | GRCh38.p7 | 19:4355095 | GCTGCCCCTCCCCAC[A/G]GTGCTGACGGTGCTC | 84954 |
| rs746836249 | snp | C/T | 2.31935e-05 | 0.00340532 | intron-variant | MPND | GRCh38.p7 | 19:4354453 | TCTAGGGGCAAGGGG[C/T]TCCGGAGCCCAGTCG | 84954 |
| rs746876088 | snp | C/T | 1.74433e-05 | 0.0029532 | synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357531 | CCCTTACTATTCTGG[C/T]AACCCAGGCCCCGAG | 84954 |
| rs747112102 | snp | C/T | 3.48894e-05 | 0.00417654 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357370 | ATGGACTACCAGCTG[C/T]GGCTGCAGGGCTCCA | 84954 |
| rs747137265 | snp | C/T | 3.86556e-05 | 0.00439617 | intron-variant | MPND | GRCh38.p7 | 19:4353073 | CAGGGGCGGATACAG[C/T]TCGGGTTGGGGAGGA | 84954 |
| rs747165299 | snp | C/T | 0.000163894 | 0.00905098 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | MPND, SH3GL1 | GRCh38.p7 | 19:4359978 | CCTGGAACAGGTGTG[C/T]GGCGTCCTCAAGCAG | 84954 |
| rs747192969 | snp | A/G | | | intron-variant | MPND | GRCh38.p7 | 19:4344187 | TTGACTGCAGGAAGA[A/G]CTCCAGTGTGAGGAG | 84954 |
| rs747220089 | snp | A/C/G | 3.41818e-05 | 0.004134 | synonymous-codon, intron-variant, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357327 | ACACAGCCCGGCGCT[A/C/G]CCATCTCTGCAGGAC | 84954 |
| rs747245996 | snp | C/T | 9.05855e-05 | 0.00672938 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4345940 | AAGGCCACCTGGCTC[C/T]GGCTGCACCAGCTGC | 84954 |
| rs747273152 | snp | C/T | 1.80036e-05 | 0.00300024 | intron-variant, downstream-variant-500B | MPND, SH3GL1 | GRCh38.p7 | 19:4359891 | ACCCCCGGGCACAGC[C/T]TGAGGCCCAGCCCCC | 84954 |
| rs747283158 | snp | A/G | 0.000100913 | 0.00710257 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4345763 | AAGAAGTTCCTGGGC[A/G]ACCTGCAGCCAGACG | 84954 |
| rs747315621 | snp | A/G | 0.000186707 | 0.00966014 | missense, intron-variant, nc-transcript-variant | MPND | GRCh38.p7 | 19:4358129 | ATGTGGAGATGGCCT[A/G]CGTCCAGGACAGCTT | 84954 |
| rs747400176 | in-del | -/GCCCTGCT | 1.76561e-05 | 0.00297115 | frameshift-variant, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357396 | TCCAGCAATGGCTTC[-/GCCCTGCT]CAGCCCTGCCTCGCC | 84954 |
| rs747464514 | snp | A/G | 0.000157462 | 0.00887166 | intron-variant | MPND | GRCh38.p7 | 19:4354145 | GTCAGACTCACCCCA[A/G]GTTCTGCCCCTGCCC | 84954 |
| rs747554042 | snp | C/G | 3.34767e-05 | 0.00409112 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4354082 | GGTGGACAGCAAGAT[C/G]CGGGTTCCGGTCCGC | 84954 |
| rs747761340 | snp | C/T | | | intron-variant | MPND | GRCh38.p7 | 19:4349699 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 84954 |
| rs747783433 | snp | C/G | 1.85146e-05 | 0.00304252 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4352950 | GGAAGAGGAGGAGGA[C/G]GACGTTCTGGCAGGG | 84954 |
| rs747799992 | snp | A/C | 6.47962e-05 | 0.00569156 | intron-variant | MPND | GRCh38.p7 | 19:4346020 | GAAGCCGCCCAGGTC[A/C]CTGTGGAATGAGGGG | 84954 |
| rs747937769 | snp | C/G | 2.31699e-05 | 0.00340359 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4343917 | GGCGCGCTCACCAGG[C/G]GCGCGGTCACACTGC | 84954 |
| rs747954418 | snp | G/T | 6.35849e-05 | 0.00563812 | intron-variant | MPND | GRCh38.p7 | 19:4346017 | CAGGAAGCCGCCCAG[G/T]TCACTGTGGAATGAG | 84954 |
| rs748009479 | snp | A/G | 3.7287e-05 | 0.00431765 | intron-variant, splice-acceptor-variant | MPND | GRCh38.p7 | 19:4354947 | GTTCCTCCCTTCCCC[A/G]GGACTTCCACAGTCA | 84954 |
| rs748037243 | snp | G/T | 3.32088e-05 | 0.00407471 | intron-variant | MPND | GRCh38.p7 | 19:4355035 | GAGTGGGTATCCAGG[G/T]CCAGGTGGGCGGGGG | 84954 |
| rs748124568 | snp | C/T | 1.73531e-05 | 0.00294555 | synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357543 | TGGCAACCCAGGCCC[C/T]GAGTCCAAGATCTCA | 84954 |
| rs748222304 | snp | C/T | 3.62845e-05 | 0.00425922 | intron-variant | MPND | GRCh38.p7 | 19:4354161 | GTTCTGCCCCTGCCC[C/T]AGCTCACCTGGATCT | 84954 |
| rs748236149 | in-del | -/G | 7.90483e-05 | 0.00628632 | frameshift-variant, downstream-variant-500B, nc-transcript-variant | MPND, SH3GL1 | GRCh38.p7 | 19:4359966 | CCTGTGTCACGTCCT[-/G]GAACAGGTGTGCGGC | 84954 |
| rs748288214 | snp | C/G | | | intron-variant | MPND | GRCh38.p7 | 19:4351071 | GGTCACCTCCACAAG[C/G]GCAGTTTAGGACAGA | 84954 |
| rs748338147 | in-del | -/CCTGCGGGGCCTGTC | 1.78838e-05 | 0.00299025 | cds-indel, intron-variant, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357269 | CTACCAGAGCCTGTT[-/CCTGCGGGGCCTGTC]CCTGCGGGGCCTGTC | 84954 |
| rs748395428 | snp | A/G | 1.75271e-05 | 0.00296028 | synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4357378 | CCAGCTGCGGCTGCA[A/G]GGCTCCAGCAATGGC | 84954 |
| rs748622742 | snp | C/T | 9.35497e-05 | 0.00683858 | synonymous-codon, intron-variant, nc-transcript-variant | MPND | GRCh38.p7 | 19:4358151 | GGACAGCTTCCTGAC[C/T]AATGACATCCTTCAC | 84954 |
| rs748687076 | snp | A/G | 1.66576e-05 | 0.00288592 | missense, nc-transcript-variant | MPND | GRCh38.p7 | 19:4359163 | TCCTCTGTCCTGTAG[A/G]TGCTGCTGGTGGAGT | 84954 |
| rs748752148 | snp | C/T | 5.39311e-05 | 0.00519256 | intron-variant, synonymous-codon, nc-transcript-variant | MPND | GRCh38.p7 | 19:4354975 | TCACCTGACACGGAG[C/T]GAGGTCGTGGGTTAC | 84954 |