MPND
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs7769snpA/G0.2367240.249647intron-variant, utr-variant-3-prime, downstream-variant-500BMPND, SH3GL1GRCh38.p719:4360546TTCACTGGACCACAG[A/G]GGGAGGGGAATGTGA84954
rs15093snpA/C/T0.0003992810.0141238intron-variant, utr-variant-3-prime, downstream-variant-500BMPND, SH3GL1GRCh38.p719:4360524GCAGAGCCTGGGGTC[A/C/T]GGAGGCTTCACTGGA84954
rs1802365snpG/Tintron-variantMPNDGRCh38.p719:4349047CCACTATCCAGAACC[G/T]CCAATCTTTCGACCC84954
rs2041772snpA/G0.4845610.0864931intron-variantMPNDGRCh38.p719:4355038TGGGTATCCAGGGCC[A/G]GGTGGGCGGGGGCGT84954
rs2041773snpA/G0.4873060.0786506intron-variantMPNDGRCh38.p719:4355057GGGCGGGGGCGTTGG[A/G]GGACCGGGGTCACGG84954
rs2041774snpA/G0.4853630.084286intron-variantMPNDGRCh38.p719:4355206AGGTGGCATTCTGGG[A/G]AGGGTTGGGAAGGGA84954
rs2041775snpC/T0.4283330.175206intron-variantMPNDGRCh38.p719:4355303TGCCCGTCTGTGTGC[C/T]TGGGACCCCATGGTG84954
rs2386601snpC/T0.4831990.0901004upstream-variant-2KBMPNDGRCh38.p719:4341902GGTGATGTGCATCTG[C/T]AGTCCCAGCTAATTG84954
rs3048292in-del-/TTT00intron-variantMPNDGRCh38.p719:4355353ttttttttttttttt[-/TTT]gagacggagtctcgc84954
rs3810367snpA/C0.4829790.0906686upstream-variant-2KBMPNDGRCh38.p719:4342850TAGAAACCCTTAGTT[A/C]TGAGCGCAAACCATC84954
rs3810368snpC/T0.4155630.18732upstream-variant-2KBMPNDGRCh38.p719:4342733AGGCAGGGCCGGGCT[C/T]GTTGCGCGCCTGATC84954
rs4003316in-del-/TTintron-variantMPNDGRCh38.p719:4348277ttttttttttttttt[-/TT]ngagacggagtctcg84954
rs4435381snpC/G0.4640960.129085upstream-variant-2KBMPNDGRCh38.p719:4342288GAAAGTGCGTAAGGA[C/G]TTGGGGAAATAAACT84954
rs4806980snpC/G0.4871770.0790385intron-variantMPNDGRCh38.p719:4347172tgtttttgctgttat[C/G]gccttcaactgattg84954
rs4806981snpA/G0.4356940.167385intron-variantMPNDGRCh38.p719:4356285ATccaggcaccgggg[A/G]ttcacacctggaatc84954
rs4807583snpA/G0.03404910.125957synonymous-codon, nc-transcript-variantMPNDGRCh38.p719:4357558CGAGTCCAAGATCTC[A/G]CCTTTCTGGGTGATG84954
rs4807584snpC/T0.4839950.0880135intron-variantMPNDGRCh38.p719:4357895AGGGCCCTGGCTCTC[C/T]TCTGGGCCTCTCCCA84954
rs6510805snpG/T00upstream-variant-2KBMPNDGRCh38.p719:4343038AACGGTCCAATCATG[G/T]AATCAGTCGAGGGCC84954
rs6510806snpC/T0.3061820.243605intron-variantMPNDGRCh38.p719:4347271ttcaagacggagtct[C/T]gctctgtcgcccagg84954
rs6510807snpC/T0.4593470.136653intron-variantMPNDGRCh38.p719:4347576ACTTTTTTTTATGTA[C/T]GAAGTTTATTGCATG84954
rs7245412snpA/G0.4999540.00479211intron-variantMPNDGRCh38.p719:4345099gttgcccaggctgga[A/G]tgcagtagcatgatc84954
rs7246177snpC/T0.4530870.145793intron-variantMPNDGRCh38.p719:4353844AAAAAATTTCTTCTT[C/T]GTAAATAagagtctc84954
rs7247827snpC/T0.4081880.193589intron-variantMPNDGRCh38.p719:4350314caggtcatgcagggc[C/T]ctgtaggttatgggg84954
rs7258168snpA/G0.3160.241131intron-variantMPNDGRCh38.p719:4350200ccctggggcacgacc[A/G]tgcctggtgtgttgg84954
rs8102860snpA/G0.4992030.0199521intron-variantMPNDGRCh38.p719:4346351AACTTCAAATGCTAT[A/G]ATAATAGATGTTCCC84954
rs8108076snpC/T0.4878710.076925intron-variantMPNDGRCh38.p719:4347556CTGTAGATATGTTTT[C/T]ATAAACTTTTTTTTA84954
rs8110781snpG/T0.04639470.145069downstream-variant-500BMPND, SH3GL1GRCh38.p719:4360292GGGACCTCCTGGGGT[G/T]TGTGTGGCTTTGGAG84954
rs8112334snpC/T0.4842090.0874434intron-variantMPNDGRCh38.p719:4356764ctgcctcagcctcca[C/T]agtagatgggagtac84954
rs8113766snpG/T00intron-variantMPNDGRCh38.p719:4344800ctggaatgcagttgc[G/T]cgatctcggctcact84954
rs10401996snpA/Gintron-variantMPNDGRCh38.p719:4345165aattctcctgcctta[A/G]cctcttgagtagctg84954
rs10406751snpA/G0.4676860.122935intron-variantMPNDGRCh38.p719:4354609CAGTGGCTCACACCT[A/G]TAATCCCAGCACTTT84954
rs10407203snpA/G0.4509850.148678intron-variantMPNDGRCh38.p719:4354813AGGTTGCGGTGAGCC[A/G]AGATCGTGCCACTGC84954
rs10407866snpC/T0.4139140.188765intron-variantMPNDGRCh38.p719:4350175ttctgagaaacagcc[C/T]ctgcaaaggccctgg84954
rs10411091snpG/Tintron-variantMPNDGRCh38.p719:4346873cgtctctactaaaaa[G/T]acaaaaattagccag84954
rs10411614snpA/G0.4547840.1434intron-variantMPNDGRCh38.p719:4355511CAGCTAATTTTTTGT[A/G]TTTTTAGTAGAGACG84954
rs10412506snpA/G0.01111960.0737302intron-variantMPNDGRCh38.p719:4355915gatggagtgcagggc[A/G]cgatcttggctcact84954
rs10412616snpC/T0.4544230.143914intron-variantMPNDGRCh38.p719:4354705CCTGTCTCTACTAAA[C/T]ATACAAAAATTAGCT84954
rs10412629snpC/T0.004750570.0485048intron-variantMPNDGRCh38.p719:4346857caacatggtgaaacc[C/T]cgtctctactaaaaa84954
rs10414802snpA/G0.017390.091611synonymous-codon, nc-transcript-variantMPNDGRCh38.p719:4343730GCCGCTGTCCCCGGC[A/G]GGCGGTGCGGGCGAG84954
rs10420217snpC/T0.489950.0701706intron-variantMPNDGRCh38.p719:4355874tttttttttttttct[C/T]gagacattctcgctc84954
rs10668030in-del-/T0.50intron-variantMPNDGRCh38.p719:4347909TTGTTTTTTTTTTTT[-/T]GAGACAGACTCTCGC84954
rs11085070snpA/G0.2112120.246973intron-variantMPNDGRCh38.p719:4353177TAAGTCTGGAGCCGG[A/G]CGAGGCCTGGGCTGA84954
rs11085071snpC/T0.4840660.0878235intron-variantMPNDGRCh38.p719:4353222CCCAGTTTTACTCAC[C/T]GCCTTGACTTCTTAA84954
rs11453629in-del-/T00intron-variantMPNDGRCh38.p719:4356637TTCTTTTTTTTTTTT[-/T]CCTTTTCTTTGAGAC84954
rs11666770snpC/G0.3357880.23482intron-variantMPNDGRCh38.p719:4351655atcacaaggtcagac[C/G]atcgagaccatcctg84954
rs11666771snpA/G0.3357880.23482intron-variantMPNDGRCh38.p719:4351659caaggtcagacgatc[A/G]agaccatcctggcta84954
rs11668153snpC/T0.4556210.142197intron-variantMPNDGRCh38.p719:4352766TTCTCTGCTCCCTCC[C/T]TCCCTCTAGTGGTCA84954
rs11668187snpC/G0.3895010.256676intron-variantMPNDGRCh38.p719:4352841GGATTTAGCAGGGAG[C/G]GGGGGGGCACCCAGC84954
rs11669297snpA/Gintron-variantMPNDGRCh38.p719:4348445tttgtatttttagta[A/G]aaatggggtttcacc84954
rs11670483snpA/Gintron-variantMPNDGRCh38.p719:4349541ttgagatggagtgtc[A/G]ctcttgttgcccagg84954
rs11670560snpC/T0.03221140.122752intron-variantMPNDGRCh38.p719:4349098tttgagatggagtct[C/T]gctctgttgtccagg84954
rs11881539snpC/G0.4411580.161117intron-variantMPNDGRCh38.p719:4349659gggactacagatgcc[C/G]actaccatgcccagt84954
rs11882587snpA/G0.4858170.083007synonymous-codon, nc-transcript-variantMPNDGRCh38.p719:4352962GGAGGACGTTCTGGC[A/G]GGGGTCTCAGCAGAG84954
rs12462529snpA/G0.3181740.240525intron-variantMPNDGRCh38.p719:4359528CCCAGGGTCCTGGCC[A/G]CCCCTGAGTGTCTTA84954
rs12609239snpA/G0.04372810.141251intron-variantMPNDGRCh38.p719:4352397TGTATTATAAAATGC[A/G]AGGTGagccgggtgc84954
rs12985281snpG/Tintron-variantMPNDGRCh38.p719:4350223tgtgttggaggaaca[G/T]cgaggagcctgtgtg84954
rs12985506snpG/Tintron-variantMPNDGRCh38.p719:4350310agggcaggtcatgca[G/T]ggctctgtaggttat84954
rs16992360snpC/G0.1300080.219321upstream-variant-2KBMPNDGRCh38.p719:4342332GCTATGCTGAGTCTG[C/G]AGGCCTTGGGGATGC84954
rs17853075snpA/G0.0003606420.0134235synonymous-codon, nc-transcript-variantMPNDGRCh38.p719:4343877CGGCGGCGGGGCCGG[A/G]GCGGGGGGCTGCGGC84954
rs28725202snpA/G0.04791490.147179intron-variantMPNDGRCh38.p719:4344522GGACGTAGATTACCA[A/G]ACACCCCATCCCACA84954
rs28736724snpC/T0.2008010.245111intron-variantMPNDGRCh38.p719:4344622CTGTGGTTTCCCAGC[C/T]GTGAAATGGAATATT84954
rs34192297in-del-/Tdownstream-variant-500BMPND, SH3GL1GRCh38.p719:4360120GGGGTGAGGGTGGCT[-/T]GGGTGCCCAGGCTGG84954
rs34505344in-del-/Aintron-variantMPNDGRCh38.p719:4347262TTTTTTTTTTCAAGA[-/A]CGGAGTCTTGCTCTG84954
rs34522164snpA/G0.06030790.16284missense, nc-transcript-variantMPNDGRCh38.p719:4359194AGCCTCACGAGGTCA[A/G]GGGAACCCTTGTAGA84954
rs34875067in-del-/Aintron-variantMPNDGRCh38.p719:4345143CCTCTGCCTCCCGGT[-/A]TCAAGCAATTCTCCT84954
rs34883765in-del-/Gintron-variantMPNDGRCh38.p719:4358790GACCCTACCTCAAGG[-/G]AAAAAACCCAACAAA84954
rs35121116in-del-/Cupstream-variant-2KBMPNDGRCh38.p719:4342464CCTGAGAACATTCCC[-/C]GAGCACCCTGGAGAG84954
rs35289519in-del-/Cintron-variantMPNDGRCh38.p719:4359316GGCCCCCTGGGCAGC[-/C]TAAAAGGTGGCAGCA84954
rs35324876in-del-/Tintron-variantMPNDGRCh38.p719:4348278TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCGC84954
rs35351631in-del-/Tintron-variantMPNDGRCh38.p719:4354531GGCCTTGTCTGCTTT[-/T]GTTTGCTACTGGTAC84954
rs35424646snpA/G0.1094610.206758intron-variantMPNDGRCh38.p719:4353531CCTCGGCCTCCCAAA[A/G]TGTTGGGATTACAGG84954
rs35431326in-del-/Tintron-variantMPNDGRCh38.p719:4349401GCCTTGGTGGGAACT[-/T]GCCTGTGGAAAGCAG84954
rs35432330in-del-/Gintron-variantMPNDGRCh38.p719:4352849CAGGGAGAGGGGGGG[-/G]CACCCAGCTGAGGGT84954
rs36091183in-del-/Tupstream-variant-2KBMPNDGRCh38.p719:4342495CTCCCCCGCACCCCT[-/T]ACTGTCCAGTTCCCA84954
rs45561032snpA/Gsynonymous-codon, intron-variant, nc-transcript-variantMPNDGRCh38.p719:4358169TGACATCCTTCACGA[A/G]ATGGTGAGCTCGCTG84954
rs56331661in-del-/TT00intron-variantMPNDGRCh38.p719:4355870GCCTTTTTTTTTTTT[-/TT]CTTGAGACATTCTCG84954
rs56332006snpC/T0.04525280.143452upstream-variant-2KBMPNDGRCh38.p719:4343293CGCCCCAGGCTTCCA[C/T]CTTGCAACCTCTATC84954
rs56812200snpA/G0.2247090.248717intron-variantMPNDGRCh38.p719:4350118AGGTGACATTTGAAC[A/G]GAGAACTGAAGGTGG84954
rs56828298snpA/C0.4536970.14494intron-variantMPNDGRCh38.p719:4352376CACCAAAGGTTGCGC[A/C]GGGCTTGTATTATAA84954
rs56942202snpA/C0.06223010.165053intron-variantMPNDGRCh38.p719:4355458CTCCTGCCTCAGCCT[A/C]CTGAATAGCTGGGAC84954
rs57747211snpA/Gintron-variantMPNDGRCh38.p719:4348287TTTTTTTGAGACGGA[A/G]TCTCGCTCTGTCGCC84954
rs57770089snpA/Gintron-variantMPNDGRCh38.p719:4348281TTTTTTTTTTTTTGA[A/G]ACGGAGTCTCGCTCT84954
rs58479594in-del-/AAupstream-variant-2KBMPNDGRCh38.p719:4342053AAAAAAAAAAAAAAA[-/AA]GAAAAAAGAAAAGAA84954
rs59062816snpC/T0.0318250.122064intron-variantMPNDGRCh38.p719:4346309GGGGGCTGGAAATGA[C/T]GGCAGGGACCAGAGG84954
rs59677849snpC/T0.4958550.045338intron-variantMPNDGRCh38.p719:4349603GCAACCTCCGCCTCT[C/T]GGGTTCAGGCGATTC84954
rs60284417snpA/Gintron-variantMPNDGRCh38.p719:4348330CAGTGGCACAATCTA[A/G]GCTCACTGCAACCTC84954
rs60305318in-del-/A0.4349760.168179intron-variantMPNDGRCh38.p719:4352720AAATTACAAATAAAT[-/A]AAAAAAAATGTGAGG84954
rs60406459snpA/Gintron-variantMPNDGRCh38.p719:4349059TGGAGGTTCTGGATA[A/G]TGGACAAAAGATATA84954
rs60697121snpC/G0.2157470.247642intron-variantMPNDGRCh38.p719:4349419CTGTGGAAAGCAGTG[C/G]TGGCGGGAGAAGGCG84954
rs60930749snpC/T0.2991580.245119intron-variantMPNDGRCh38.p719:4350444GGCTGCTGTGGGGAC[C/T]AGACTGTCGGGGGTT84954
rs61167639snpA/Gintron-variantMPNDGRCh38.p719:4356324TAGGGAGGCCGAGGC[A/G]GGAGGTTTGCTGGAG84954
rs61730128snpA/G0.03956940.134978synonymous-codon, intron-variant, nc-transcript-variantMPNDGRCh38.p719:4357312GTACCACAGCCACCC[A/G]CACAGCCCGGCGCTG84954
rs61730129snpA/G0.000752420.0193815missense, nc-transcript-variantMPNDGRCh38.p719:4357349CTGCAGGACATCGAC[A/G]CACAGATGGACTACC84954
rs61730130snpA/C/G0.003267230.0402874intron-variantMPNDGRCh38.p719:4357229CAGGCCCCTGTGCCC[A/C/G]CTGAGCTGCGCCTCT84954
rs62129340snpC/T0.1970820.244335upstream-variant-2KBMPNDGRCh38.p719:4343188TTTCTCCCCTGGTCC[C/T]AAAGGCCGAGGCCTC84954
rs62129341snpA/G0.0977270.198275intron-variantMPNDGRCh38.p719:4347304GGAGTACAGTGGCAC[A/G]ATCTCAGCTCACTGC84954
rs62129342snpA/G0.4489630.151372intron-variantMPNDGRCh38.p719:4352034AAAAATTAGCCAGGC[A/G]TGGTGGTGGGCAACT84954
rs62129345snpG/T0.01387990.0821421intron-variantMPNDGRCh38.p719:4356751GTTCAACATCCTCCT[G/T]CCTCAGCCTCCATAG84954
rs67576371in-del-/Gintron-variantMPNDGRCh38.p719:4352841GATTTAGCAGGGAGC[-/G]GGGGGGGCACCCAGC84954
rs67782188snpC/G0.4651580.127307intron-variantMPNDGRCh38.p719:4351575ACAGATAAGAATAGA[C/G]TTGGCGGCCGGGCAC84954
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