iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

RAB40B

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs200533601	snp	A/C			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665903	AACAAAAAAAAAAAA[A/C]AAAAAAAAAAACTAC	10966
rs200562369	in-del	-/C			intron-variant	RAB40B	GRCh38.p7	17:82695210	TTCTTTTTTTTTTTT[-/C]GAGACAAAATCTCAC	10966
rs200588385	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82679748	GTCACCGAGCACAGG[A/G]CAGGGGGCAGCCTCC	10966
rs200627779	snp	C/T	1.91985e-05	0.0030982	missense, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698485	ACGGGGACTCGGCCG[C/T]GCCATCCTGCAGGCT	10966
rs200629575	snp	G/T			synonymous-codon	RAB40B	GRCh38.p7	17:82657971	GGTGGAGCTGGTGGT[G/T]AGGGAGTAGGAACCG	10966
rs200685409	in-del	-/T			intron-variant	RAB40B	GRCh38.p7	17:82695839	TGATATCAGTTTTTT[-/T]CTACAGCAGCTCAGG	10966
rs200686541	in-del	-/G			intron-variant	RAB40B	GRCh38.p7	17:82689968	AAAACTTCATCTCAA[-/G]AAAAAAAAAAAAAGA	10966
rs200823862	in-del	-/A	0.0158469	0.0875917	intron-variant	RAB40B	GRCh38.p7	17:82680497	TTTGCTTCTGAAGTT[-/A]AAAAAAAATATCGCA	10966
rs200923067	in-del	-/TT			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82670535	TAAAAGAATTCCTGA[-/TT]TTTTTTTTTTTTTTT	10966
rs200946319	snp	C/T					GRCh38.p7	17:82655950	GGGTCCCTTAAATTT[C/T]TTTTTTTTTTTTTTT	10966
rs200952278	snp	C/T			intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661914	AAAAAAAAAAAGGAA[C/T]AAACAAATGAGGGTG	10966
rs200956653	in-del	-/AG			intron-variant	RAB40B	GRCh38.p7	17:82675394	ACGTGGTCTCCACCA[-/AG]CGCTGGCTTCCTTCA	10966
rs200966226	in-del	-/C			intron-variant	RAB40B	GRCh38.p7	17:82685808	CTTCTTCTTCTTCTT[-/C]TTTTTTTTTTTTTGA	10966
rs201043195	snp	A/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671321	GTAACTCTAACACAC[A/T]CACACGCTCTCTGTA	10966
rs201153359	snp	A/G	0.00081042	0.0201135	intron-variant	RAB40B	GRCh38.p7	17:82664565	TCGATGCCTGCGGAA[A/G]GGTTAGAGACGGCTT	10966
rs201160141	snp	A/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671649	CTCTAACACACACAC[A/T]CACACCCTGTACTCA	10966
rs201162076	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82659662	AGGATCACACCCTGG[A/G]GGAGAGGTCACAGGC	10966
rs201169084	snp	C/T	0.000132371	0.00813438	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657841	CTGGAGAGATTCCGC[C/T]GTGTTTCTTTCAGTG	10966
rs201202897	in-del	-/AGAGAC			intron-variant	RAB40B	GRCh38.p7	17:82696053	TTTTGTATTTATAGT[-/AGAGAC]AGGGTTTCTCCATGT	10966
rs201217503	in-del	-/C			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671574	TGACACACCCCACCC[-/C]TGTAACTCTAACACA	10966
rs201252583	snp	A/G/T	0.000399281	0.0141238	missense, synonymous-codon, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698542	CGCTGTCGCCCACCA[A/G/T]CAGGAACTTGAGCAG	10966
rs201302225	snp	C/T					GRCh38.p7	17:82656063	AAGTGATTCTCCTGC[C/T]TCAGCCTCCTGAGTA	10966
rs201352520	snp	A/G	0.0168555	0.0902422	synonymous-codon, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698465	CTCACCCGCCGGGTG[A/G]CCGTACGGGGACTCG	10966
rs201402014	in-del	-/A			intron-variant	RAB40B	GRCh38.p7	17:82676311	AACAGCCTCTCCCTC[-/A]CACACAGTGAGGGCA	10966
rs201411340	snp	A/G			intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660686	TACCTGCACACACAT[A/G]TACACACACACACAC	10966
rs201456706	snp	C/T	1.64749e-05	0.00287005	missense	RAB40B	GRCh38.p7	17:82657936	ACGAGCTTCACTTTG[C/T]GGAGGCTGCTCCTTT	10966
rs201456802	snp	A/G	0.00895958	0.0663288	synonymous-codon, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698489	GGACTCGGCCGCGCC[A/G]TCCTGCAGGCTCGCC	10966
rs201518137	in-del	-/AAC	0.0130921	0.0798413	intron-variant	RAB40B	GRCh38.p7	17:82691686	GACTCCATCTCAAAA[-/AAC]AACAACAAAAAAATG	10966
rs201529197	in-del	-/G	0.0948562	0.196037	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82700413	TGGGATTGCAGCACT[-/G]TTTTTTTTTAGAAGG	10966
rs201532849	in-del	-/G	0.00636936	0.0560724	intron-variant	RAB40B	GRCh38.p7	17:82681284	TTGCTGGCTCTCCTA[-/G]GGAACATAACTTACC	10966
rs201618975	in-del	-/GTAC			intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660686	TACCTGCACACACAT[-/GTAC]ACACACACACACACA	10966
rs201630625	snp	A/T			intron-variant	RAB40B	GRCh38.p7	17:82672237	CTCTAACACACACAC[A/T]CACACGCTCCCTGTA	10966
rs201640296	snp	A/C/G	0.00538721	0.0516203	missense	RAB40B	GRCh38.p7	17:82658649	GCCTGCTCCGTGGGC[A/C/G]CCTGCCGCTTGAACG	10966
rs201771680	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82658802	CTGGGTCGAGGAACC[C/T]CCCACGAGTTCATGT	10966
rs201785078	in-del	-/AA			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671478	GTAACTCTAACACAC[-/AA]ACTCACATGCTCCCT	10966
rs201799464	in-del	-/AAAAAAAAAAAAAA			intron-variant	RAB40B	GRCh38.p7	17:82681021	GCAAGACTCCATCTC[-/AAAAAAAAAAAAAA]AAAAAAAAAAAAAAA	10966
rs201809864	snp	A/G	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82693954	CAGGCGTGGTGGCGC[A/G]CACCTGTAGTCCCAG	10966
rs201888700	in-del	-/AC			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671205	ACCCCCGTAACTCTA[-/AC]ACACACACTCACACG	10966
rs201908639	snp	A/C/T	0.0166325	0.0896639	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671224	CACACTCACACGCTC[A/C/T]CTGTACTCACTGACA	10966
rs201933331	snp	A/C			intron-variant	RAB40B	GRCh38.p7	17:82672377	CCCACTGACACACCT[A/C]ACCCCTGTAACTCTA	10966
rs201937312	snp	A/T			intron-variant	RAB40B	GRCh38.p7	17:82681390	CTGGGAGAAGTCTCC[A/T]AATACAGGAAGCAGT	10966
rs201968958	snp	C/T	0.011928	0.0763002	missense, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698467	CACCCGCCGGGTGGC[C/T]GTACGGGGACTCGGC	10966
rs202005555	in-del	-/TGCT			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82672073	TCTAACACACACACA[-/TGCT]CCCTGTACTCACTGA	10966
rs202007349	snp	C/T	0.00187846	0.0305893	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657796	TCTGAGATGCATCCA[C/T]CAGCTGCCGGGGGTA	10966
rs202010805	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82695005	AAAGGACTTTGGTGA[A/G]CACTGACTGTATTTA	10966
rs202015683	snp	A/C			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671205	CACCCCCGTAACTCT[A/C]ACACACACTCACACG	10966
rs202021296	snp	A/T			missense	RAB40B	GRCh38.p7	17:82659614	CATCGATCAATGCCG[A/T]CAAAAGACCAGCGGT	10966
rs202083767	in-del	-/C	0.0310518	0.120672	intron-variant	RAB40B	GRCh38.p7	17:82687075	ACTCTTGTCTGTGGG[-/C]CCCCCCACACCCCCG	10966
rs202136186	snp	C/T	4.95094e-05	0.00497517	missense	RAB40B	GRCh38.p7	17:82659585	TACAACATACCTCAT[C/T]GATCTCCTTAATCCA	10966
rs202141202	in-del	-/AC			intron-variant	RAB40B	GRCh38.p7	17:82672393	ACCCCTGTAACTCTA[-/AC]ACACACACTCACACG	10966
rs202179634	snp	A/C	0.0341408	0.126114	intron-variant	RAB40B	GRCh38.p7	17:82691898	GAACCGGGGACCCAG[A/C]TGCCAGACGGAAATG	10966
rs202197961	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82682439	AAATGGAGAGACATA[C/T]CATGTTCATGATTGA	10966
rs202202395	snp	A/C	1.6609e-05	0.0028817	intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660958	TTCAAAGTTGGTTTG[A/C]TCTCCCAGCTCGGGG	10966
rs202229377	snp	C/T	6.62131e-05	0.00575345	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657838	CTCCTGGAGAGATTC[C/T]GCCGTGTTTCTTTCA	10966
rs367547171	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82698749	CGCGCATCCCCGCCC[A/G]GCCCCGCCATTGGTG	10966
rs367559472	in-del	-/G			intron-variant	RAB40B	GRCh38.p7	17:82697845	CCGCTGTCGTGGGGG[-/G]TCCCCTCTTCCGCAC	10966
rs367586370	snp	C/T	1.65677e-05	0.00287812	missense	RAB40B	GRCh38.p7	17:82658571	AACGACTCTGTGATG[C/T]TGAAATTGCACAGAG	10966
rs367594533	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665639	TGGGAGGCTGAGGCG[A/G]GTGGATCACTTGAGG	10966
rs367605685	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82674378	GGTTCACGCCTGTAA[C/T]CCCAGCACTTTGGGA	10966
rs367606138	snp	C/T	0.00199481	0.0315187	intron-variant	RAB40B	GRCh38.p7	17:82689904	CCCAGGAGGCGGAGG[C/T]TGCAGTGAACCGAGA	10966
rs367666038	in-del	A/CC			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666589	TTCCCCGCCCCCATC[A/CC]CCCCCCAGACACCAG	10966
rs367727780	snp	A/G			upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699643	TGCATGTGTGTGTCT[A/G]CGTGTGCTGCTTCTA	10966
rs367750435	snp	A/C			intron-variant	RAB40B	GRCh38.p7	17:82672118	CCTGTAACTCTAACA[A/C]ACACACTCACACGCT	10966
rs367829136	in-del	-/AC			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671528	ACCCCTGTAACTCTA[-/AC]ACACACACTCACACG	10966
rs367883440	snp	C/T	0.00279162	0.0372561	intron-variant	RAB40B	GRCh38.p7	17:82679899	GCTGCGGGGTGAACG[C/T]AGTCGTGGGAGGCTC	10966
rs367927498	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82659261	GCAGGCACAAGCGCC[A/G]GTCACTGCTGGTCAG	10966
rs367993539	snp	A/C			intron-variant	RAB40B	GRCh38.p7	17:82688092	GACTTTACATCCCTG[A/C]AAGTTTTCATTTCAT	10966
rs368011144	snp	C/T	0.000149775	0.00865247	utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698615	GACGGCCCGGCGCCC[C/T]CACCCATGCCCGGCC	10966
rs368029606	snp	A/G/T	0.000381648	0.0138088	intron-variant	RAB40B	GRCh38.p7	17:82659530	AATTCCTGGCCTGAC[A/G/T]TCCTCCCAAGCCTAC	10966
rs368030118	snp	G/T					GRCh38.p7	17:82654688	CTTAGTAGCTGGGAC[G/T]ATAGACGTGCACCAC	10966
rs368046933	in-del	-/GTGCAGCGCCT			intron-variant	RAB40B	GRCh38.p7	17:82667440	GATCTGAGCACACCT[-/GTGCAGCGCCT]TCCATGAGATCCCGA	10966
rs368059082	snp	C/T	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82672882	TTTTTCCTTCATGTA[C/T]GAATTTTTGTTTCTA	10966
rs368141240	in-del	-/TC			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82670177	CTTGAGGGCCAACAA[-/TC]TTTTTTTTTTTTTTT	10966
rs368202804	in-del	-/AGGTTGCAG			intron-variant	RAB40B	GRCh38.p7	17:82680963	GAACCCGGGAGGCAG[-/AGGTTGCAG]TGAGCTGAGATTGCG	10966
rs368234823	multinucleotide-polymorphism	AG/CA			intron-variant	RAB40B	GRCh38.p7	17:82675395	ACGTGGTCTCCACCA[AG/CA]CGCTGGCTTCCTTCA	10966
rs368260821	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668326	AGCACCGAGTCCTCC[C/T]TCCAGTCTGCAGGAC	10966
rs368269917	snp	C/T	0.000363721	0.0134807	intron-variant	RAB40B	GRCh38.p7	17:82664560	TGTAGTCGATGCCTG[C/T]GGAAGGGTTAGAGAC	10966
rs368284283	snp	C/T			utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657472	TAATATCAGTGACTC[C/T]AAATTATCCCGCTGC	10966
rs368350438	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82658858	TCGTTTGGAAAGACC[A/G]TCTTTGCAGACGTAA	10966
rs368480661	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82674892	GAGAAAGAACAACAC[A/G]AGATAATCCTGACGG	10966
rs368650402	snp	A/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82667608	GAGTCCAGGCTTCCC[A/G]CATCCTCCTCTGTCT	10966
rs368721257	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82695269	TGATCTCAGCTCACT[C/T]CACCCTCCACCTCCT	10966
rs368753593	snp	A/C	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82659436	GCCGAGGTGAGGCAC[A/C]CTCCTTCCTGCTGGA	10966
rs368758904	in-del	-/G			upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699876	GGCAGCAGGCAAAGG[-/G]CGAGCTCCGTCCAAG	10966
rs368810423	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666055	CACCACACCTGCCAC[C/T]GCACCTGCCACCGCA	10966
rs368856048	snp	C/T	0.000429944	0.0146556	intron-variant	RAB40B	GRCh38.p7	17:82659684	GTCACAGGCTCAGCA[C/T]GCAGAACACAGATGC	10966
rs369008504	in-del	-/C					GRCh38.p7	17:82655950	GGGTCCCTTAAATTT[-/C]TTTTTTTTTTTTTTT	10966
rs369025134	snp	A/G	0.00517822	0.0506191			GRCh38.p7	17:82656412	CCTGGAGGTCTTTGC[A/G]GTCAGCCCTGCTCTG	10966
rs369034439	snp	A/C	0.000437904	0.0147905	intron-variant	RAB40B	GRCh38.p7	17:82659714	CAGGCACAGCTGTGG[A/C]CATGCACGCAAAGAC	10966
rs369141216	snp	A/G	6.62976e-05	0.00575712	intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660977	CCCAGCTCGGGGGAT[A/G]CTGTGTTACCTGTGC	10966
rs369148363	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82674357	AAAGAAAAGACCAGG[C/T]GTGGTGGTTCACGCC	10966
rs369337904	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82691107	GGTGTGTCCACGCAC[C/T]GTGTAGTCTTGAGGG	10966
rs369406308	snp	C/T			intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660634	ACGTGCACACACACA[C/T]GCACAGGCACTCATG	10966
rs369423690	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669753	GGCCCTGTGAAATTA[C/T]GCTTTGAGCGACGAC	10966
rs369619558	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82672374	GTACCCACTGACACA[C/G]CTCACCCCTGTAACT	10966
rs369710621	snp	C/T	0.00108819	0.0233005	synonymous-codon	RAB40B	GRCh38.p7	17:82659631	AAAAGACCAGCGGTT[C/T]GCAATGTCATAGACC	10966
rs369729721	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82684750	CTACAAAGAGGCTGC[A/G]GAAACTTCTGCGTGG	10966
rs369739761	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82697474	ACGCCCGGCTGCCCT[C/T]CTCCGCCCAGGACTC	10966
rs369740049	snp	A/G			upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699371	TTCGTGTGTGTGCAT[A/G]TCTGCGTGTGCATGT	10966
rs369893955	in-del	-/ACAC	0.00615884	0.0551497	intron-variant	RAB40B	GRCh38.p7	17:82660353	CCTGCACGCACGTGT[-/ACAC]ACACACACGCACAGG	10966
rs369957603	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82697135	GGTCGTGAGCCCAAG[C/T]CCATCTCAGCTGCTC	10966
rs370010463	snp	C/T	8.28151e-05	0.00643433	missense, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660997	GTTACCTGTGCGCCC[C/T]GGGAGTAGGAGCGGA	10966
rs370126318	snp	C/T	0.000153988	0.00877328	intron-variant, utr-variant-5-prime, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661081	ACCATTAAGAAGAAA[C/T]CAGTGCTTCTTCCTG	10966
rs370178602	in-del	-/GAC	0.000798403	0.0199641	intron-variant, cds-indel	RAB40B	GRCh38.p7	17:82662634	GTGTGACCTTGCTCA[-/GAC]GACAGTGTGGACAGA	10966
rs370354454	snp	C/T	3.35396e-05	0.00409496	splice-acceptor-variant	RAB40B	GRCh38.p7	17:82658135	CTTGCAAGCTCAGCA[C/T]TTGGGAGAGAAAAGA	10966
rs370400007	snp	C/T	0.00199481	0.0315187	intron-variant	RAB40B	GRCh38.p7	17:82696235	CTTTATTACAAAGCA[C/T]TGGACCATTGTTTTG	10966
rs370574771	snp	C/G			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82672043	GTACTCACTGACACA[C/G]CCCACCCCTGTAACT	10966
rs370629319	snp	C/T	0.0185938	0.0946107	intron-variant	RAB40B	GRCh38.p7	17:82659075	GGGAAGTGGCCCTGC[C/T]GACACCTTGGTTTTG	10966
rs370705080	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666802	GCTTAGTAACAAGAC[A/G]TGACCAGCCTTTGTG	10966
rs370711029	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82676702	GCGTGATCTCAACTC[A/G]CTGCAACCTCCGCCT	10966
rs370720504	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82692058	CAGTGGGGCCCGCAC[A/G]GTCCGTGGGCTGAGG	10966
rs370730379	snp	G/T			intron-variant	RAB40B	GRCh38.p7	17:82694673	TGAGACAAAAAGAAA[G/T]AATTCCTCAGAAATT	10966
rs370731022	snp	A/C/T			intron-variant	RAB40B	GRCh38.p7	17:82697504	CAGAGCGGGTCTCTG[A/C/T]TGGAAGCGTGGGTTC	10966
rs370747679	snp	A/T			upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699705	TTGTGCATCCATGCA[A/T]GTGTTTGCGTGCGTG	10966
rs370769484	snp	C/G	1.66228e-05	0.0028829	missense	RAB40B	GRCh38.p7	17:82658600	AGGGCTGACCTCAAA[C/G]AAGGTCACGCCCAGG	10966
rs370825483	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671955	TGACACAGCTCACCC[C/T]GTAACTCTAACACAC	10966
rs370842700	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82664181	CGGGGGCGCTGTGCC[A/G]ACGGTGGTGGGGGAA	10966
rs370858079	snp	A/G	5.11592e-05	0.00505737	intron-variant	RAB40B	GRCh38.p7	17:82658444	CCGCTGACCCACCTC[A/G]GCATCTGGAGGGCAG	10966
rs370911172	in-del	-/AGACAGG			intron-variant	RAB40B	GRCh38.p7	17:82696055	TTGTATTTATAGTAG[-/AGACAGG]GTTTCTCCATGTTGA	10966
rs371076784	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82679788	AGGGCAGGGGCCAGC[C/T]TCCACTGAGCTGTCA	10966
rs371107577	snp	A/G	6.58989e-05	0.00573978	synonymous-codon	RAB40B	GRCh38.p7	17:82658048	TGAGGTGGCTTCTTA[A/G]GGCAATGGGGAGCGG	10966
rs371166576	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82696591	AATCTCCAGCCCTGT[C/T]CTCCAGGCGCTCAAT	10966
rs371285285	snp	A/G			upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699645	CATGTGTGTGTCTGC[A/G]TGTGCTGCTTCTATG	10966
rs371387694	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82686800	GCAGCCCATCCAAAA[A/G]CCACTTCACTCAGCA	10966
rs371389878	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669274	TGAGGTCAGGAGTTC[A/G]AGAGCAGCCTGACCA	10966
rs371514659	snp	A/G	0	0	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665958	CAGGGTCTCCCCCTC[A/G]CCCAGGCTCTAGTAC	10966
rs371520038	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82683502	TTTCAAAATAAGCAA[A/G]AGAGGCCAGACATAG	10966
rs371570390	snp	C/T					GRCh38.p7	17:82655286	CCTTGCTACATGTTC[C/T]GCTTCTGGGGACTTC	10966
rs371644752	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82693553	ACCCAGCGATTCACA[C/T]GCATAGGGACCTTTC	10966
rs371681301	in-del	-/A	0.00772909	0.0616831	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657655	TCCCTTTACAAACAC[-/A]ACATCGAAAACAAGA	10966
rs371714347	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82676373	ACACAGTGAGGGCAC[C/T]CCTCACCTTCAACAG	10966
rs371749878	in-del	-/C					GRCh38.p7	17:82655138	AGGAGTTTCCTGAGG[-/C]CTGCCGTAACAATCG	10966
rs371761626	snp	A/T			intron-variant	RAB40B	GRCh38.p7	17:82684844	CGGGGCCAGGCACGG[A/T]GGCCCACGCCTGTAA	10966
rs371784781	snp	C/T	0.000118346	0.00769149	synonymous-codon	RAB40B	GRCh38.p7	17:82658642	GGCCTGGGCCTGCTC[C/T]GTGGGCACCTGCCGC	10966
rs371788068	snp	C/T	3.32452e-05	0.00407695	intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660943	TTGTAAATGTTATTA[C/T]TCAAAGTTGGTTTGA	10966
rs371898931	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82670912	GTCATGGATGCTCAC[A/G]GTCTGAAGTGCTGTC	10966
rs371901791	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82679084	GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATA	10966
rs371963506	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82674336	AAAGAGTGAAACTCC[A/G]TCTCAAAAGAAAAGA	10966
rs372054252	snp	A/G/T	1.65015e-05	0.00287237	synonymous-codon	RAB40B	GRCh38.p7	17:82659586	ACAACATACCTCATC[A/G/T]ATCTCCTTAATCCAT	10966
rs372457103	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82673037	GGTGAAACCTCATCT[C/T]TACTAAAAATACAAA	10966
rs372549893	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82674459	ACAGGGTGAAACCCC[A/G]TCTCTAGTAAAAATA	10966
rs372568527	snp	A/G			intron-variant, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82696468	CATATTCGTCTGGGC[A/G]TACACGTTGTTGGGT	10966
rs372603297	in-del	-/C			intron-variant	RAB40B	GRCh38.p7	17:82676445	CAGCCTCTCCCCCCC[-/C]ACACAGGGCACCCCC	10966
rs372664626	in-del	-/A	0.35894	0.225016	intron-variant	RAB40B	GRCh38.p7	17:82674476	CTCTAGTAAAAATAC[-/A]AAAAAAAAAAAAATT	10966
rs372670635	snp	A/C			intron-variant	RAB40B	GRCh38.p7	17:82697583	AGCCTCAGGGTCGGC[A/C]TCGTCCAAGCTGTTC	10966
rs372670673	in-del	-/CTTG			upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699688	GTGTGCGTGCGCTTG[-/CTTG]TTTGTGCATCCATGC	10966
rs372756823	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82660039	TTGTGCACAGATGCA[C/T]GCACACACAGTGCAC	10966
rs372769515	snp	A/G	8.2373e-05	0.00641714	missense	RAB40B	GRCh38.p7	17:82657937	CGAGCTTCACTTTGC[A/G]GAGGCTGCTCCTTTT	10966
rs373058507	in-del	-/AC			intron-variant	RAB40B	GRCh38.p7	17:82660566	CGTGTACACACACAC[-/AC]GCACAGGCACTCATG	10966
rs373168157	snp	C/T	0.000149282	0.00863822	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657816	TGCCGGGGGTAACGC[C/T]GAGCTTCTCCTGGAG	10966
rs373305091	snp	G/T	1.81587e-05	0.00301314	intron-variant, utr-variant-5-prime, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661089	GAAGAAACCAGTGCT[G/T]CTTCCTGACAACAGG	10966
rs373348210	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82673985	CCCTTCTTTGAAATT[A/G]TTGTTTTCAATGTCC	10966
rs373467950	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671766	CACACTCACATGCTC[C/T]CTGTACCCACTGACA	10966
rs373545721	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82674811	ACCAGGTGGGAAGAA[C/T]GAACCCCAGAATGAA	10966
rs373554826	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82691304	GATTGGAGAAGACAA[C/T]GAGGCCCTCATGCTG	10966
rs373709578	snp	C/T	0.000166628	0.00912612	intron-variant	RAB40B	GRCh38.p7	17:82664472	CCTGGGGGTGCGGGA[C/T]GCTCGCACCTCCTCC	10966
rs373744689	in-del	-/A	0.0955749	0.196603	intron-variant	RAB40B	GRCh38.p7	17:82685121	CTGTCTCAAAAAAGG[-/A]AAAAAAAAAACAAAA	10966
rs373804585	snp	G/T			utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657646	GTACTAATTTTCCCT[G/T]TACAAACACACATCG	10966
rs373945595	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666068	ACCGCACCTGCCACC[A/G]CACCTGCCACCACAC	10966
rs374004107	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82697158	AGCTGCTCCCCCAAA[C/T]TCTGCCCATTCCTCA	10966
rs374079323	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82684894	CGAGGCGGGTGGATC[A/G]CCTGAGGTCAGGAGT	10966
rs374112410	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82674205	ATTAGCCGGGTGTGG[C/T]GGCGGGTGCCTGTAA	10966
rs374147807	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82675082	CTGGAGAGAGAGAGA[A/G]AAAACATCTGACACC	10966
rs374228684	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82664375	GTGTTCCCGGGGGCG[C/T]TGTGCCGATGGTGGT	10966
rs374233144	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82672130	ACACACACACTCACA[C/T]GCTCCCTGTACCCAC	10966
rs374238825	snp	A/C/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671979	AACACACACACTCAC[A/C/T]CACTGACACAGCTCA	10966
rs374244317	snp	C/T	1.64961e-05	0.00287189	missense	RAB40B	GRCh38.p7	17:82659611	ATCCATCGATCAATG[C/T]CGTCAAAAGACCAGC	10966
rs374248219	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82685684	TTCCTTCATGAGAAC[A/G]AAACTGTCCTTTCGG	10966
rs374328212	snp	C/T			utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657067	ACCGGTCGCCAACTC[C/T]ACCAAGAGAGAAACA	10966
rs374345452	snp	A/G	4.95405e-05	0.00497673	missense, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82664541	AGCAGGATGGTGGTC[A/G]TCTTGTAGTCGATGC	10966
rs374405886	in-del	-/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82670534	TAAAAGAATTCCTGA[-/T]TTTTTTTTTTTTTTT	10966
rs374410879	snp	C/T	1.65636e-05	0.00287776	synonymous-codon	RAB40B	GRCh38.p7	17:82658558	GGCCAGCTCCGTGAA[C/T]GACTCTGTGATGTTG	10966
rs374431939	snp	G/T			intron-variant	RAB40B	GRCh38.p7	17:82682235	ATCAAAATATACAAG[G/T]CCAACATGGAAAAAA	10966
rs374432795	snp	A/C			intron-variant	RAB40B	GRCh38.p7	17:82684220	AGTGAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA	10966
rs374437976	snp	A/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665756	CCTGGAATCCTAGCT[A/T]GTAGGGAGGCTGAGG	10966
rs374522893	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82695690	CACTCCAGCCTGGGC[A/G]GCAGAGAAGACCCTG	10966
rs374791193	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82690887	TGTGCACGTTTGCCC[C/T]GGGGGAGCATGGAGT	10966
rs374869472	snp	A/G	8.29153e-05	0.00643823	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657817	GCCGGGGGTAACGCC[A/G]AGCTTCTCCTGGAGA	10966
rs374905655	snp	C/G	0.0360663	0.129354	intron-variant	RAB40B	GRCh38.p7	17:82689796	AGATGGTGAAACCCC[C/G]TCTCCACTAAAACTA	10966
rs374963145	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82689230	GGGCAGGAGGAGCAG[C/T]GAGCAGGTGCGGCTG	10966
rs375148547	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82664251	AGCTTGCTCCCTGGG[A/G]TGCTGGGCCGATGGT	10966
rs375155459	snp	C/T	0.00119737	0.0244387	intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660742	CGCATACACAGTGCA[C/T]GTACCTGCACACACG	10966
rs375156395	in-del	-/GG			intron-variant	RAB40B	GRCh38.p7	17:82684116	TCCCAGCTACTCGGG[-/GG]AGGCTGAGGCAGGAG	10966
rs375262445	snp	C/T	1.68258e-05	0.00290045	missense	RAB40B	GRCh38.p7	17:82658655	TCCGTGGGCACCTGC[C/T]GCTTGAACGCCAGGT	10966
rs375316050	in-del	-/CTTT			intron-variant	RAB40B	GRCh38.p7	17:82695197	TTTCTTTCTTTCTTT[-/CTTT]TTTTTTTTTCGAGAC	10966
rs375405932	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82659986	GATTGCACGCATACA[C/T]GTGCACATACACATG	10966
rs375437090	in-del	-/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671354	GACACACCTCACCCC[-/T]GTAACTCTAACACAC	10966
rs375670934	snp	C/T	0.00159617	0.0282053	intron-variant	RAB40B	GRCh38.p7	17:82667526	CTCTGCTTCCTCCTC[C/T]GGGCCCTGCCCCCTT	10966
rs375682761	snp	C/T	1.70467e-05	0.00291943	intron-variant	RAB40B	GRCh38.p7	17:82658446	GCTGACCCACCTCGG[C/T]ATCTGGAGGGCAGAG	10966
rs375691236	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82692496	AGACAGAGTCTGACC[C/T]GGGGCACACACACAA	10966
rs375749687	in-del	-/AC			intron-variant	RAB40B	GRCh38.p7	17:82660550	CACATACCTACACAC[-/AC]GTGTACACACACACA	10966
rs375759024	snp	A/C			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665895	AGAACAACAACAAAA[A/C]AAAAAAAAAAAAAAA	10966
rs375811676	in-del	-/A			intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661889	AGACTCTGTCTCAGA[-/A]AAAAAAAAAAAAAAA	10966
rs375830089	in-del	-/ACA			intron-variant	RAB40B	GRCh38.p7	17:82679974	GTGGCTGTGGGAGGG[-/ACA]GAGGGGCCAGATCCC	10966
rs375898721	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82683528	CATAGTGGCTCACAA[C/T]TGTAATCCCACCACT	10966
rs375906632	snp	C/T	0.00199481	0.0315187			GRCh38.p7	17:82654739	TATTTTTAGTAGAGA[C/T]GGGGTTTCATCATGT	10966
rs375940080	snp	C/T	0.00199481	0.0315187	intron-variant	RAB40B	GRCh38.p7	17:82690239	AGGGAGCACGGAGTG[C/T]GCACACGTGTTCTCG	10966
rs376058247	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82684146	GAATCGCTTGAACCC[A/G]GGAGGCAGGGGTTGC	10966
rs376076189	snp	A/G	0.000149727	0.00865107	intron-variant	RAB40B	GRCh38.p7	17:82664477	GGGTGCGGGACGCTC[A/G]CACCTCCTCCAGACT	10966
rs376078290	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82672683	TCTGCCAGGTTATGA[C/T]GCAGCAGGAGGCCCT	10966
rs376257474	snp	C/T			utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657598	CATGATAAAGTAACA[C/T]TCAGAATTTCATGTT	10966
rs376275028	snp	A/G	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82684238	AAAAAAAAAAAAAAA[A/G]TTACAATGAGATACC	10966
rs376349673	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82692782	AAACACTGATAATTT[A/G]GATTATGTTAAAATT	10966
rs376397106	in-del	-/C			intron-variant	RAB40B	GRCh38.p7	17:82659029	GCCCAGGGTTGCTGG[-/C]CACCGCCGAGAGCTG	10966
rs376414275	snp	C/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82658239	CCCAAGGCTCGGACG[C/G]CCGTGGCCCTGGCTT	10966
rs376458704	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82687751	TCCTGACTGGCTGCC[A/G]ATCATGCAGGGCAGG	10966
rs376519150	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82688149	TTCTCTCTGCCAGCC[A/G]GGGCCCAAAACACAC	10966
rs376702290	snp	C/G			upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699285	TTCATCCAGGGCCTC[C/G]TCGTTGCCCCATTTA	10966
rs376735416	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82700678	ATAGGGGTCAGGAGG[C/T]CCCCAGCCCACCCTC	10966
rs376750161	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82673986	CCTTCTTTGAAATTA[C/T]TGTTTTCAATGTCCA	10966
rs376902718	snp	A/G			intron-variant, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82696542	CCAGACCCCGAGGGC[A/G]CAGTGCAGACAAAGC	10966
rs376915725	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671555	ACACGCTCCCTGTAC[C/T]CACTGACACACCCCA	10966
rs376923678	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82685062	GGGTTGCAGTGAGCC[A/G]AGATCATACCATTGC	10966
rs376928314	snp	A/G			upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699704	TTTGTGCATCCATGC[A/G]TGTGTTTGCGTGCGT	10966
rs376936564	snp	C/T	0.000746312	0.0193028	intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660969	TTTGATCTCCCAGCT[C/T]GGGGGATGCTGTGTT	10966
rs376996242	snp	A/T	1.9235e-05	0.00310115	intron-variant, utr-variant-5-prime, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661097	CAGTGCTTCTTCCTG[A/T]CAACAGGTTCTGGAA	10966
rs377055626	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82697691	TCCTGGGTTCCTGCC[C/T]CCGCCTTTCTTTCCC	10966
rs377082964	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82679828	GACACCTGGAAACAC[A/G]AAGGAACACGGCCCA	10966
rs377175854	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82674265	GAGTCACTGAGGCTG[A/G]GAGGCGGAGGTTGCA	10966
rs377221335	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82684681	GCCAGGTTCAAAGGC[C/G]TCCGGGATGCAGGCA	10966
rs377318011	snp	C/T	0.00835141	0.0640778	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669213	GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC	10966
rs377345816	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82688763	ACATAGTGAAACCCC[A/G]TCTTTACTAAAAATA	10966
rs377473041	snp	C/T	0.00953873	0.0683987	intron-variant	RAB40B	GRCh38.p7	17:82660496	ACGTGTACACATACA[C/T]GCACATGCAGGCACT	10966
rs377552070	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82695474	GGATTACAGCTGTGA[A/G]CCACTGCGCCCGGCT	10966
rs377564544	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666981	TCTAAAGGGAAGCGC[A/G]CCGCTGAGAGGCCGA	10966
rs377594845	snp	C/G					GRCh38.p7	17:82654601	GTCACTCAGGCTGGA[C/G]TGCAGTGGTGCAATC	10966
rs377595645	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666744	GAGCACTGCCTTCCT[A/G]AAACCAGGTACAATG	10966
rs377623305	snp	C/T	1.65679e-05	0.00287814	missense, downstream-variant-500B	RAB40B	GRCh38.p7	17:82661016	AGTAGGAGCGGAATA[C/T]GGTACAAAATCTTCC	10966
rs377625038	snp	C/T	0.00199481	0.0315187	intron-variant	RAB40B	GRCh38.p7	17:82663982	GGGGCGCTGTGCCGA[C/T]GGTGGTGGTGGGAGG	10966
rs377649519	snp	A/G	1.64735e-05	0.00286993	synonymous-codon	RAB40B	GRCh38.p7	17:82658025	GCCGTTGGCCATCGA[A/G]AAGGACTTGAGGTGG	10966
rs377744506	in-del	-/TA			intron-variant	RAB40B	GRCh38.p7	17:82694560	ACATACACACACACA[-/TA]CACACACACACCTGG	10966
rs377754104	snp	A/G	8.46819e-05	0.00650644	intron-variant	RAB40B	GRCh38.p7	17:82658471	GCAGAGGTGGCCCCC[A/G]GAATAGCCCCTGGGC	10966
rs386799998	multinucleotide-polymorphism	CA/TG			intron-variant	RAB40B	GRCh38.p7	17:82660447	GCACAGGCACTCATG[CA/TG]GATGCACGCATACAC	10966
rs386799999	in-del	ATGTAC/GT			intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660684	CGTACCTGCACACAC[ATGTAC/GT]ACACACACACACACA	10966
rs386800000	multinucleotide-polymorphism	AG/CA			intron-variant	RAB40B	GRCh38.p7	17:82675394	ACGTGGTCTCCACCA[AG/CA]CGCTGGCTTCCTTCA	10966
rs386800001	in-del	CTA/GCAG			intron-variant	RAB40B	GRCh38.p7	17:82679776	TCCACCAAGCACAGG[CTA/GCAG]GGGCCAGCTTCCACT	10966
rs386800002	multinucleotide-polymorphism	CA/GG			intron-variant	RAB40B	GRCh38.p7	17:82682140	ACACACACACACACA[CA/GG]CACGCATGCACACAC	10966
rs386800003	multinucleotide-polymorphism	AT/TC			intron-variant	RAB40B	GRCh38.p7	17:82682774	TAAAGAATAGTCTTT[AT/TC]AACAAATGCTGCTGG	10966
rs386800004	multinucleotide-polymorphism	CTCA/GCCG			intron-variant	RAB40B	GRCh38.p7	17:82690409	GTGTGCACATGTGTT[CTCA/GCCG]GGGAGCAGAGAGTGT	10966
rs386800005	in-del	A/GC			intron-variant	RAB40B	GRCh38.p7	17:82691897	TGAACCGGGGACCCA[A/GC]TGCCAGACGGAAATG	10966
rs386800006	in-del	A/GT			upstream-variant-2KB	RAB40B	GRCh38.p7	17:82700413	TGGGATTGCAGCACT[A/GT]TTTTTTTTAGAAGGA	10966
rs397825181	in-del	-/CA			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671277	ACACACAGTCACACA[-/CA]TCCTGTACTCACTGA	10966
rs397856466	in-del	-/T			intron-variant	RAB40B	GRCh38.p7	17:82678880	GCTCCCTTTCTGCGT[-/T]TTTTTTTTTTTTTTT	10966
rs397952171	in-del	-/ATTT			intron-variant	RAB40B	GRCh38.p7	17:82676961	TTTATTTATTTATTT[-/ATTT]TTTCTGAGACGGAGT	10966
rs398031788	in-del	-/G	0	0			GRCh38.p7	17:82654900	CTTAAGAGAAGAAAG[-/G]TGTGTAAGAATCTGT	10966
rs398031791	in-del	-/TTTT	0	0	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666258	CAATACATTTTTTTT[-/TTTT]GAGATGGAATTTCGC	10966
rs398031792	in-del	-/CA	0	0	intron-variant	RAB40B	GRCh38.p7	17:82682138	ACACACACACACACA[-/CA]GGCACGCATGCACAC	10966
rs527289793	snp	A/G	3.30262e-05	0.0040635	synonymous-codon, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82664527	CCCGCCGCCCGTCCA[A/G]CAGGATGGTGGTCGT	10966
rs527292213	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82670033	ACTCCAGCTTTGATA[C/T]GTCTGTCTCCAGACG	10966
rs527366782	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82677201	ATCCACCTGCCTCGG[C/T]CTCCCAAAGTGCTAG	10966
rs527382210	snp	G/T	0.00159617	0.0282053	intron-variant	RAB40B	GRCh38.p7	17:82675125	AAAAGCTACAAAGGA[G/T]GCATTTTCACATCTT	10966
rs527431128	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82659342	ATAGCCGAGGTACGC[C/T]GTGGACGCTCGTTTC	10966
rs527439412	snp	A/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82679928	TCACGAAGAGACATC[A/G]TCTTGGGGAAGGGGG	10966
rs527443419	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82686314	ATGGGATTTCCCCAT[A/G]TTGGCCAGGCTGGTC	10966
rs527516570	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82680401	CGGCAGTTCCCCCAC[A/G]TGTGTGAGCTTCTCA	10966
rs527523884	in-del	-/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671792	GACACAGCTCACCCC[-/T]GTAACTCTAACACAC	10966
rs527550092	snp	C/T	0.000399281	0.0141238			GRCh38.p7	17:82655194	AAATATTTATTTTCT[C/T]GTAGCTCTGGAAGCC	10966
rs527572868	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82691072	ACAGAGGGGAGGGCC[A/G]GGCCCTGCACCTGCA	10966
rs527578123	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82686045	CTGAACTCGTGATCT[A/G]CCCGCCTTGGCCTCC	10966
rs527645216	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82682331	GTAGCCCCCAAACCA[C/T]GAAATACTTGAGTAT	10966
rs527703696	snp	G/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82676432	CCCTCACCTTCAACA[G/T]CCTCTCCCCCCCCAC	10966
rs527782248	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82687089	GCCCCCCCACACCCC[C/T]GATGATGCCCAGATC	10966
rs527849219	snp	G/T	0.00199481	0.0315187	intron-variant	RAB40B	GRCh38.p7	17:82691751	GGGACACAATCTGGT[G/T]TTGGAAGCACCAGCT	10966
rs527852275	snp	A/T	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82697762	CTCAAACTTGGGGGA[A/T]CCCCGGGCTGCCTGC	10966
rs527876973	snp	C/T	0.000399281	0.0141238			GRCh38.p7	17:82656467	TCTTCATGCGGAATT[C/T]CTGACAGCCCCTCGG	10966
rs527915905	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82692234	GGGGCCCGCACGGTC[C/T]GTGGGCTGAGGTGAC	10966
rs527920750	snp	A/C	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82686850	TCCTCCACGTTCCTC[A/C]CGTCCAGTGCTGGGG	10966
rs527959276	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82664755	CCGGGCCCCTCCTGT[C/T]CTCAGCCGCCTTGGC	10966
rs527983475	snp	C/T	0.00199481	0.0315187	intron-variant	RAB40B	GRCh38.p7	17:82697470	CTCCACGCCCGGCTG[C/T]CCTCCTCCGCCCAGG	10966
rs528007208	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82660530	GCACAGATGCATACA[C/T]AGTGCACATACCTAC	10966
rs528052926	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82685066	TGCAGTGAGCCGAGA[C/T]CATACCATTGCACTC	10966
rs528127388	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82658903	GCCGCACTGAATTAG[A/G]GCCCTCATCTAATGA	10966
rs528360272	snp	C/T	0.00159617	0.0282053	intron-variant	RAB40B	GRCh38.p7	17:82667239	CAGGAGGCAGTGTGC[C/T]GAGTTCCTGGTCTCC	10966
rs528388283	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82700090	GTTTACTTTGGAATG[C/T]CAATTTAGTTTGCAA	10966
rs528434869	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82686492	AATGGCTAGTGTTCT[C/T]ATAAGCACAGAGAGA	10966
rs528439514	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82692899	ACAAAGGACTCACAG[C/T]CAGAATCTATATTTT	10966
rs528494807	snp	A/G	0.00795532	0.062565	intron-variant	RAB40B	GRCh38.p7	17:82690747	GGGAACAGAGAGTGT[A/G]CACGTGTGTCCAGGG	10966
rs528514551	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82674194	AAAAATACAAAATTA[A/G]CCGGGTGTGGTGGCG	10966
rs528538357	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668816	CAGGGAAGGCGGAGC[C/T]GCTGCCTGATCCGTG	10966
rs528617816	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82680375	TGGGCGGGGCCGCTC[A/G]GGGGACGGGACGGCA	10966
rs528670573	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668506	AGCCACCCTCAGCCC[C/T]CCCTCAGCTTCCCTC	10966
rs528680184	snp	A/C/G	0.00159617	0.0282053	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661653	GCGCTTTGGGAGACC[A/C/G]AGGCAGGCGGATCAC	10966
rs528746514	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82663967	CTGGGGGTGCTCCCC[A/G]GGGCGCTGTGCCGAC	10966
rs528767993	snp	C/T	0.00159617	0.0282053	intron-variant	RAB40B	GRCh38.p7	17:82679118	TCGATCTCCTGACCT[C/T]GTGATCCACCTGCCT	10966
rs528769006	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82673936	TCTCTCTTTTTCCCA[A/G]CATTCTGGGAATTCA	10966
rs528846644	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82698787	GTTGCTAGGGCAGCT[A/G]CGCGCTTTCACTGGC	10966
rs528875539	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661571	GTACTGGGACCCACA[A/G]AGACCAGAACGGAGC	10966
rs528983456	snp	C/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82697942	GGTCTCCCCTCCCCT[C/G]CGACCCACGCGCAGA	10966
rs528984209	snp	A/C	0.00755907	0.0610114	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665904	ACAAAAAAAAAAAAA[A/C]AAAAAAAAAACTACA	10966
rs528998147	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82691843	GCCTTCCTTCTACCC[C/T]TGCCTGGAGAGAAAT	10966
rs529056480	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82670565	TTTGAGACGGAGTCT[C/T]ACTCTGTCGCCCAGG	10966
rs529291633	snp	C/T			intron-variant, downstream-variant-500B, missense	RAB40B, MIR4525	GRCh38.p7	17:82667847	CTGACCCACCCAGTA[C/T]GAGGCTTTCCTGAGC	10966
rs529308320	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82673118	CTGAGGCAGGAGAAT[C/T]GCTTGAACCCGGCAG	10966
rs529308364	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82687931	AAAATAATTAGCCGG[C/G]CATGGTGGCATGCAC	10966
rs529314774	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666911	CTGGCCTCACTCTCG[G/T]CTGTGATCGGATGTT	10966
rs529334413	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669312	GAAACCTTGTCTCTG[C/T]TAAAAATACGAAATT	10966
rs529398292	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82688342	GTTTTGGGCCGGGCA[C/T]GGTAGCTCACGCCTG	10966
rs529457187	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82672658	GAGCTGACGGGCTTG[C/T]GCGATGCCCTCTGCC	10966
rs529515093	snp	A/C	0.00795532	0.062565	intron-variant	RAB40B	GRCh38.p7	17:82683770	GACTTGCACCACTGC[A/C]CTCCAGCCTGGGCAA	10966
rs529542936	snp	A/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82687862	GGATCGCTTGAGCCC[A/T]GAAATTCAAGACAAG	10966
rs529715290	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668903	TAGATGGGCCACTGC[C/T]ACCATCAGCATCTTA	10966
rs529731276	snp	A/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82679894	AGCAGGCTGCGGGGT[A/G]AACGCAGTCGTGGGA	10966
rs529761925	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660654	AGGCACTCATGCAGA[C/T]GTATGCACAGTGCAC	10966
rs529847877	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82685625	GGCTCCAGTGCTGAA[A/G]CTCCAAGAAGAGGGG	10966
rs529862149	snp	A/G	0.00318978	0.0398085	intron-variant	RAB40B	GRCh38.p7	17:82686004	AGACGGGGTTTCACC[A/G]TGTTGGCCAGGCTGG	10966
rs529888189	snp	C/T	0.00795532	0.062565	intron-variant	RAB40B	GRCh38.p7	17:82664011	GGGTGTTCCCGGGGG[C/T]GCTGTGCCAACGGTG	10966
rs529890246	snp	C/G	0.000399281	0.0141238			GRCh38.p7	17:82655161	AACAATCGCCACAAA[C/G]CTGGTGACTTAAATA	10966
rs529938109	snp	A/G	0.00159617	0.0282053	intron-variant	RAB40B	GRCh38.p7	17:82695853	TTCTACAGCAGCTCA[A/G]GCCAAGTAGACAATA	10966
rs530089464	snp	C/T	0.000798403	0.0199641			GRCh38.p7	17:82655810	TGGACTTTGTCCCCG[C/T]GGCTGCCGTGCCCAG	10966
rs530159070	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82660471	GCATACACAGTGCAA[A/G]TACCTGCACACGTGT	10966
rs530216847	snp	A/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82691661	CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCC	10966
rs530280581	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82696754	CGCTCAATCTCCAGC[C/T]CTGTCCTCCAGGCGC	10966
rs530309107	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82664717	CCCAAGCTCACAGGG[A/G]CCCTGCCTGCGCCCT	10966
rs530343736	snp	A/G	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82691293	CCAGGAGAAAGGATT[A/G]GAGAAGACAATGAGG	10966
rs530356882	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82664489	CTCGCACCTCCTCCA[A/G]ACTCACCAGAGCTGC	10966
rs530473639	snp	C/T	0.000273387	0.0116884	intron-variant	RAB40B	GRCh38.p7	17:82658151	TTGGGAGAGAAAAGA[C/T]AAACCTTGCTTAGTG	10966
rs530544456	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82684566	GGGTGGGTGATGGAC[C/T]GTGGTTCATCTCTAC	10966
rs530609684	snp	A/G	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82667152	GGCTGCGGAGGCCAC[A/G]GTTCTCAAGCAGCTT	10966
rs530618521	snp	C/T	0.0228947	0.104514	intron-variant	RAB40B	GRCh38.p7	17:82693830	GCTCACGCCTGTAAT[C/T]CCAGCACTTTGGGAG	10966
rs530747190	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82686732	GAGAATAAATCTCTG[C/T]TTCAATTTGTCCAAA	10966
rs530761253	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82693443	GGAAGATGATGCAGC[C/T]GGGGCCTCCAGCTTT	10966
rs530786356	in-del	-/AC	0.430515	0.172957	intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660694	CACACATGTACACAC[-/AC]ACACACACACAGGCA	10966
rs530793943	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82672460	GGATATTCCATTCTA[C/T]ACTGTCATAACCAGG	10966
rs530800725	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82663942	CAGAGAAGCCCTGGT[C/G]CAGCTGGGGCTGGGG	10966
rs530809106	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82688178	ACTAAGTCACCATCA[C/T]GCCCAGCTAATTTTT	10966
rs530864440	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666695	AACATGGAAAGAGAG[A/G]GTTTGAGTTAAGGGG	10966
rs530895193	snp	A/C			intron-variant	RAB40B	GRCh38.p7	17:82682422	TCAAAGAAGACCTAA[A/C]TAAATGGAGAGACAT	10966
rs530907443	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82693360	GTATGAAAAGGTGCT[C/T]AGTCATCAGAGAAAT	10966
rs531003155	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RAB40B, MIR4525	GRCh38.p7	17:82667774	ACGCCCGAAGCACCC[A/G]CTTTGCAGACGCCAC	10966
rs531014770	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82673806	ATCTGGAGACACAAA[C/T]CTCAATTTTGGGGAA	10966
rs531014983	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665818	GTTGCAGTGAACTGA[A/G]ATTGTGCCACTGTGC	10966
rs531060127	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82663547	GGGGGAGGGAGAGGT[A/G]CCCCGGGCTTGCCCC	10966
rs531062986	snp	A/G			intron-variant, missense	RAB40B	GRCh38.p7	17:82662453	CTGGGACAACGTGCC[A/G]GCCTCCTGGGCCGCT	10966
rs531089738	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82684982	ACCCGGGCGTGGTGG[C/T]AGGCGCCTATAATCC	10966
rs531228186	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82692320	AGATCCAAGAACTCT[A/G]CCCTGCAACTACAGA	10966
rs531241886	snp	A/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82697832	ACCCGCTCTCCGGCC[A/G]CTGTCGTGGGGGGTC	10966
rs531273674	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82676163	TCAAAATGTGTGCAC[C/T]TGCTGCCAGCAGTCC	10966
rs531275500	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82670147	CTGACTTAGAAAGTA[A/T]CCTCTTGACCTGTCC	10966
rs531322844	snp	A/C	0.00159617	0.0282053	intron-variant	RAB40B	GRCh38.p7	17:82660567	GTGTACACACACACA[A/C]GCACAGGCACTCATG	10966
rs531328392	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665348	GCCTCCACAGCCCAG[A/G]CTCAAGTGATCCTCC	10966
rs531333773	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82664858	ACCTGGAGGCCGGTG[G/T]GTTTGCCGCGGGGCT	10966
rs531350574	snp	C/G	0.000399281	0.0141238			GRCh38.p7	17:82655275	TCGGGGAGCCTCCTT[C/G]CTACATGTTCCGCTT	10966
rs531543263	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82681679	CCATCAATAAAAAAT[A/G]TACCAAATTCGGCAA	10966
rs531613421	snp	A/C/T	0.00318978	0.0398085	intron-variant	RAB40B	GRCh38.p7	17:82686666	AGCCTGCCAAGGGAG[A/C/T]GTGGCCCAGGCAACA	10966
rs531740157	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82677098	GGATTACAGGCGCCC[A/G]CCACCACGCCCAGCT	10966
rs531742106	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671179	CACATCCTGTACTCA[A/C]TGACACACCCCACCC	10966
rs531744255	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82670868	GCCCTACGAGTTTCA[A/C]AACCATCTTTCGTTT	10966
rs531750960	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82692651	TGCCTCAGGCCTCAC[C/T]CCAGCTGGAGGCAGC	10966
rs531754149	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82683586	TGAGCCCAGGATCTC[C/T]TGAGGATCTCTCAAG	10966
rs531811450	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82682910	AGCACTTTGGGAGAC[C/T]GAGGCAGGCAGATCA	10966
rs531940453	snp	A/G	6.76762e-05	0.00581666	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657764	TCGCAAGCAGCATTC[A/G]CCGAGAGGAACCGGG	10966
rs531949782	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82687786	TTCAAGACTTTACGC[C/T]CCCAGCCAGGCGCGG	10966
rs532165341	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82679797	GCCAGCTTCCACTGA[A/G]CTGTCACCACCACAG	10966
rs532165867	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82695079	ATACAGAAGCAAGGG[C/T]TATAAACCTGGACAA	10966
rs532226299	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82690226	TCTGCAGAATTGGAG[A/G]GAGCACGGAGTGTGC	10966
rs532287689	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82679153	CTCCCAAAGTGCTGG[A/G]ATGACAGGCGTGAAC	10966
rs532291332	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82689669	AGTGGTACCGCAGGA[A/G]GTAAAGAAGTAGAAA	10966
rs532310494	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668579	AGGGCTGGTGTGTCC[A/G]TGCTGCCCCAAGTGT	10966
rs532365899	snp	A/C	0.00478085	0.0486577	intron-variant	RAB40B	GRCh38.p7	17:82685137	AAAAAAAAAACAAAA[A/C]AACTCAAGAAGGGAG	10966
rs532393038	snp	C/G			downstream-variant-500B	RAB40B	GRCh38.p7	17:82656686	TGATGTCTACACCAG[C/G]CAGTGGCGCAGTGAA	10966
rs532402471	snp	C/T	0.000399281	0.0141238			GRCh38.p7	17:82655749	CTCCAGACACTGTCC[C/T]CTCAGGGTTCACCTT	10966
rs532422028	snp	C/T	0.00318978	0.0398085	intron-variant	RAB40B	GRCh38.p7	17:82663454	CCCCAGAGCTGGAAC[C/T]GCAGGAGCTCCCCCC	10966
rs532504265	snp	A/G	0.00279162	0.0372561	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657456	AAAAAGACCCCTCTC[A/G]TAATATCAGTGACTC	10966
rs532558650	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82697161	TGCTCCCCCAAACTC[C/T]GCCCATTCCTCACCC	10966
rs532568776	in-del	-/AC	0.00953873	0.0683987	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671364	ACCCCTGTAACTCTA[-/AC]ACACACACTCTCACA	10966
rs532577405	snp	A/G	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82664302	CGGGGTGCTGTGCTG[A/G]TGGTGGTGGGGCTGG	10966
rs532634308	snp	G/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82690788	AGAATTGGAGGGAGA[G/T]GAAGTGTGCATGTGT	10966
rs532673080	in-del	-/CA			intron-variant	RAB40B	GRCh38.p7	17:82694082	AGCGAGACTCCATCT[-/CA]AAAAAAAAAAAAAAA	10966
rs532826752	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82679620	TTTGTCTTAGGACAC[C/T]AAACTCCCAAAAGGT	10966
rs532881773	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82692889	CACACAGCCGACAAA[A/G]GACTCACAGCCAGAA	10966
rs532895881	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82662038	TACATCAATGGGAGA[C/T]TCCCCAGTGGGCCAG	10966
rs532903235	snp	C/T			intron-variant, utr-variant-5-prime, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661098	AGTGCTTCTTCCTGA[C/T]AACAGGTTCTGGAAC	10966
rs532909456	snp	A/G	0.00159617	0.0282053	intron-variant	RAB40B	GRCh38.p7	17:82693337	CCAAAGAGGAATTTC[A/G]CATAGACGTATGAAA	10966
rs532973282	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665960	GGGTCTCCCCCTCGC[C/T]CAGGCTCTAGTACAG	10966
rs533060292	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82670596	CTGGAGTGCAGTGGC[A/G]CGATCTCAGCTCATT	10966
rs533064802	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699391	CGTGTGCATGTGTGC[C/T]TCTGCAGATATCTGC	10966
rs533110043	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82688396	GAGGCGGGTAGATCA[C/T]GAGGTCAGGAGTTCG	10966
rs533180775	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RAB40B, MIR4525	GRCh38.p7	17:82667760	CAGCAGCACTGAGAA[C/T]GCCCGAAGCACCCGC	10966
rs533187774	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82700699	GCCCACCCTCGGGGT[C/T]ACACCCAGCAGTCCA	10966
rs533196033	snp	C/T	0.00199481	0.0315187	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82698881	AAAGGTCGCTGTCAC[C/T]ACAGCCAATGGAGGC	10966
rs533237803	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82676902	AAGTGCTGGGATTAT[A/G]GGCGTGAGCTACCGC	10966
rs533307235	snp	G/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82677197	CGTGATCCACCTGCC[G/T]CGGCCTCCCAAAGTG	10966
rs533308351	snp	A/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82673739	CTGCACACCTTGTGG[A/G]CCTTGCTGTAGGGAT	10966
rs533367535	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82677674	TCCAGGGCCAGCACC[C/T]AAGCGTTTGGGGTTT	10966
rs533439221	snp	A/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82683866	AAAAGATCTGAAAAG[A/T]CACTTCACCAAAGAG	10966
rs533508965	in-del	-/ACACACAC	0.01759	0.0921172	intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660688	CCTGCACACACATGT[-/ACACACAC]ACACACACACAGGCA	10966
rs533544445	snp	A/G/T	0.0023933	0.0345097			GRCh38.p7	17:82655343	GCCTCCGGGCGGCCC[A/G/T]TGCATTCGGTGAACA	10966
rs533560968	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82659835	GTGATATTTCATAAG[C/T]TCAGTGATAAACCCT	10966
rs533707101	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82674448	CATCCTGGCTAACAG[A/G]GTGAAACCCCGTCTC	10966
rs533827677	snp	A/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82696957	CACCACGGTCCTAGA[A/G]ACCTGCCACCGAGCG	10966
rs533860439	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82664180	CCGGGGGCGCTGTGC[C/T]GACGGTGGTGGGGGA	10966
rs533898591	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669912	CATACATATTTGCTC[C/T]ATAATAGCAATCCTC	10966
rs533917985	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82664363	GGTGGTGGGAGGGTG[C/T]TCCCGGGGGCGCTGT	10966
rs533996934	snp	A/G	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668676	GGCGTGGGGAGTGAG[A/G]AGAGGCCAGGCATTT	10966
rs534030437	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82675392	TGACGTGGTCTCCAC[C/T]AAGCGCTGGCTTCCT	10966
rs534142524	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82691407	ACATGTGCAAAAGGC[C/T]GGGCGCGGTGGCTCA	10966
rs534197802	snp	G/T	0.000399281	0.0141238			GRCh38.p7	17:82655369	GAACACCTCCAAAGA[G/T]CTCTGAGTCACAAAG	10966
rs534282738	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82677799	ACCCCAGATGAGGGC[A/G]TCAGTGATGCTGCGG	10966
rs534345880	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82673435	GCCCCCACTCCCTTA[C/T]TGCTGGATTCCATCC	10966
rs534360330	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82686438	CAGATGTAATCAAGT[C/T]AAGATGAGGTCATAC	10966
rs534442920	in-del	-/TTGCTCGGCCGCCAGAGCCGGTCCATCCCATGCTGGGCCTACCC	0.00558655	0.0525553	frameshift-variant	RAB40B	GRCh38.p7	17:82658492	CCCCTGGGCCTACCC[lengthTooLong]TTGCTCGGCCGCCAG	10966
rs534476773	snp	A/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82660247	ACGCAGTTCATGTGT[A/G]CACATGCATGCACAT	10966
rs534502782	snp	A/G/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82686198	CTCACTGAAACCTCC[A/G/T]CTTCCGGGGTTCAAG	10966
rs534542607	snp	C/T	0.000399281	0.0141238			GRCh38.p7	17:82655893	CTCCTGTCTGGGCCT[C/T]GGTTCCACCATCTCT	10966
rs534560944	snp	C/T	0.0130921	0.0798413	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699001	GGGGGTGGGGCCGGG[C/T]GTTTACACTCTCGCG	10966
rs534586026	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82662109	GGTGGGACGCGGCAT[G/T]GTTTTGCTGTTTGTG	10966
rs534617787	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82693491	GTGAAAAATGCTTTG[C/T]GAGAATCTACTACAG	10966
rs534639182	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82687720	GTCAAGCACAGGGTT[C/T]CTGGAAAACCAGCCC	10966
rs534644328	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82658218	CCACACCTGTTCTCC[C/T]GCCCTCCCAAGGCTC	10966
rs534666783	snp	C/T	0.00636936	0.0560724	intron-variant	RAB40B	GRCh38.p7	17:82690311	AGAATTGGAGGGAGA[C/T]GGAGTGTGCATGTGT	10966
rs534670423	snp	A/G	0.00159617	0.0282053	intron-variant	RAB40B	GRCh38.p7	17:82685351	TCCTCAACTGTGGCC[A/G]TGCACTCAACTGAAC	10966
rs534714379	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82677435	AGAAAGCATTACAAG[C/T]CGGGCTGCTTCCAGG	10966
rs534729836	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82685638	AAGCTCCAAGAAGAG[A/G]GGACCCACAGGGTCC	10966
rs534775702	snp	A/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82688621	CTCCGTCTCAAAAAT[A/T]CATAAATAAATAAAC	10966
rs534778213	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82659036	GGTTGCTGGCACCGC[C/T]GAGAGCTGGGAGAGG	10966
rs534805417	snp	A/G/T	0.00835684	0.0641614	intron-variant	RAB40B	GRCh38.p7	17:82658276	GCAGCAAGCCCTGCC[A/G/T]CGACGTCCCCTCTGC	10966
rs534856724	in-del	-/GAG	0.00398564	0.0444627	intron-variant	RAB40B	GRCh38.p7	17:82659944	TAATCGCCACCTCTC[-/GAG]GAGTGTGGCCCACTC	10966
rs534896193	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82663600	ACAGCTGAGAGAGCA[A/G]AGCCAGCAGCCCCAG	10966
rs535030175	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82663082	CAGGACAGGGGCTGA[C/T]GGCAACCCCAACGCC	10966
rs535032487	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B, synonymous-codon	RAB40B, MIR4525	GRCh38.p7	17:82667881	CCAAACGTTTGCCAC[C/T]GAGCCCAGCAGGCAC	10966
rs535047680	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82692378	GAGAATCCAGGCCTC[A/G]CTGACCGTATCGGAG	10966
rs535047730	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82693722	CACCATGAGAATTAA[C/T]ACCCCACAGCCTCAC	10966
rs535055317	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82686959	CATGGAAGACCCTCC[C/T]GTCCAGTGCTGGGGG	10966
rs535066863	snp	C/T			intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660756	ACGTACCTGCACACA[C/T]GTGTACATGCACACA	10966
rs535094077	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82686319	ATTTCCCCATGTTGG[C/T]CAGGCTGGTCTCGAA	10966
rs535094296	in-del	-/TCT	0.00518028	0.0506291	intron-variant	RAB40B	GRCh38.p7	17:82678057	AATTTGTGAGAAGAC[-/TCT]TCTTTTCATAAGCCC	10966
rs535096725	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82688640	AAATAAATAAACAAA[C/T]AGTTTTGTTTGGGCC	10966
rs535116022	snp	A/G	0.00159617	0.0282053	intron-variant	RAB40B	GRCh38.p7	17:82687164	ACGCAATTTGAACCC[A/G]TGAGTGTACCACAGT	10966
rs535139764	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82681982	TTTTCCCCATGAAAA[C/T]ATCCACTCTTACCAC	10966
rs535179821	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82691868	AGAAATGGAACTTCC[A/G]AGGGGAAAGAGCGTG	10966
rs535227192	snp	A/G	1.88503e-05	0.00306998	intron-variant	RAB40B	GRCh38.p7	17:82658729	CTAGCGGGCAGGAGA[A/G]AGGCGAGGAGCATGG	10966
rs535272664	snp	A/G	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82697012	GCAGCGGCGCCTGGG[A/G]ACAGGTAGAGACGCA	10966
rs535347810	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669844	GCCAAGTCCTGCAGC[C/T]GTCAGCAATGAACAC	10966
rs535692514	snp	C/T	0.00792852	0.0624612	intron-variant	RAB40B	GRCh38.p7	17:82676959	TTATTTATTTATTTA[C/T]TTTTTCTGAGACGGA	10966
rs535692565	snp	C/G			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671057	ACATTCCTACTTCCT[C/G]ACATTTCAGTTTTAG	10966
rs535718396	snp	A/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82663061	CAGCTGGCGGAGGGT[A/G]GGGAGCAGGACAGGG	10966
rs535874448	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82664150	GTGCCGATGGTGGTG[A/G]TGGGAGGGTGTTCCC	10966
rs535999324	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666120	CACCTGCCACCGCAC[C/T]TGGCTAATTGACAGG	10966
rs536011260	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82678705	AGACTGGCGGTCCCC[A/G]GGGCAGAGGGGAGGG	10966
rs536073423	snp	A/G	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82695564	AAAAAAAAAAACATG[A/G]CCAGGTGCTGTGGCT	10966
rs536080270	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82670852	GATGGTCTTTTTAAG[C/G]GCCCTACGAGTTTCA	10966
rs536137981	snp	A/C	0.00676609	0.0577691	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82698926	GGGGCGGAGCCAGAA[A/C]AAGCAGGAGGCGGGG	10966
rs536143396	snp	A/G	0.0228947	0.104514	intron-variant	RAB40B	GRCh38.p7	17:82685232	GGGGAGGGGGAGGGA[A/G]GACGGAGGAGGGAGG	10966
rs536205885	snp	C/G	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82674894	GAAAGAACAACACGA[C/G]ATAATCCTGACGGCA	10966
rs536270819	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82675331	CACACCCACAACCTG[C/G]CCTGGCAAATGACCA	10966
rs536329957	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B, utr-variant-5-prime	RAB40B, MIR4525	GRCh38.p7	17:82668091	CTGAGTGTTAGAACA[A/G]CTCAGGGGAGACCCA	10966
rs536347202	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82680125	CGTCCTGCTCAGACC[A/G]GAGGCCTGGCAGGGT	10966
rs536372953	in-del	-/A	0.00318978	0.0398085	intron-variant	RAB40B	GRCh38.p7	17:82688459	TCTATTAAAAATACC[-/A]AAAAAATTAGCCAGG	10966
rs536390755	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668663	CACGACTGGAGCGGG[C/T]GTGGGGAGTGAGGAG	10966
rs536459664	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82679210	TCAGGAGCAGCTCGC[A/G]CCCACCAGCAACCAC	10966
rs536482886	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82686160	TCCAGGCTGGAGGCT[A/G]GAGTGCAGTGGCACG	10966
rs536511558	snp	A/C	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82659435	TGCCGAGGTGAGGCA[A/C]CCTCCTTCCTGCTGG	10966
rs536546759	snp	C/T	0.00080048	0.01999	intron-variant	RAB40B	GRCh38.p7	17:82678056	CAATTTGTGAGAAGA[C/T]TCTTCTTTTCATAAG	10966
rs536662872	snp	C/T	0.0232847	0.105357	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671642	CCCGTAACTCTAACA[C/T]ACACACTCACACCCT	10966
rs536663022	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82677357	TCGTAAAAGCTCATT[A/G]CAATGAGATTCCCCT	10966
rs536800677	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82673573	TCTTCCTTGTGTTTG[C/G]ACAGGCATACAATTG	10966
rs536806868	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82690816	TGTGTTCCTGGGGAA[C/G]AGAGAGTGTGCACGT	10966
rs536808712	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82687276	AAATTTCATACTCTT[C/T]ATACTTATCTATTTA	10966
rs536919456	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82664344	GGGGTGCTGTGCCGA[C/T]GGTGGTGGTGGGAGG	10966
rs536946516	snp	A/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82696261	TTTTGGTTCGTCCTC[A/T]GTTCGGCATGTAGCA	10966
rs536976059	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657535	AATCACTCCAATATC[A/T]CCGTTCTTACAAAAG	10966
rs536996839	snp	A/G			synonymous-codon	RAB40B	GRCh38.p7	17:82657920	GCTCTGGGGGGGGCG[A/G]ACGAGCTTCACTTTG	10966
rs537009951	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82689291	GCTCCAGCTGCGTCC[A/G]CTCTGCACCACGGTG	10966
rs537138715	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82683208	TCATAAATGTAAAAT[C/T]TAAAATTATAAAATT	10966
rs537205425	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82689014	CTTTGGATGCTGTTG[C/T]TCTTTTCAGGTTTTG	10966
rs537206704	snp	C/G	0.00358779	0.0422022	intron-variant	RAB40B	GRCh38.p7	17:82678634	TATTCATCTCTCAGC[C/G]CAGCTTTTGAGAAAT	10966
rs537217817	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82692974	AAACAGACATAAGAC[C/T]TGGGCATTTTTCTTC	10966
rs537248115	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82667399	CCACTGATGCAGCCA[C/T]GAGCACGTGCATGGC	10966
rs537262711	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82660152	GTACTCATGCACAGA[C/T]GCACACAGTGCATAC	10966
rs537264633	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666091	CACCACACCTGCCAC[C/T]GCACCTGCCACCACA	10966
rs537285794	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82700405	CAAAATGCTGGGATT[C/G]CAGCACTGTTTTTTT	10966
rs537323750	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82672812	TACAGCAACAGAAAA[C/T]GACACCAGGTAGACG	10966
rs537341623	in-del	-/C	0.00119737	0.0244387	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657545	ATATCACCGTTCTTA[-/C]AAAAGCAGTTATTTT	10966
rs537409814	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82670216	TTTGAGACAGAGTCT[C/T]GCTCTCTCACCCAGC	10966
rs537431368	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82658973	GGAGGCCATGTTACG[C/T]GAAGGCAGAGGCTGG	10966
rs537558487	snp	G/T	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82696982	CGAGCGGGGAGGGGG[G/T]TAGGACATGCGGGGG	10966
rs537630478	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699725	TTGCGTGCGTGCTGG[A/C]GGAGAGCATTGGGTG	10966
rs537644764	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82664374	GGTGTTCCCGGGGGC[A/G]CTGTGCCGATGGTGG	10966
rs537728884	snp	A/C	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82674866	AGGGTGTGTGCAGGG[A/C]GTAGGCAGAGGAGAA	10966
rs537783479	in-del	-/C	0.00478085	0.0486577	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699905	AGAAGAAGGATAATG[-/C]CCCCACTACTTCATC	10966
rs537793622	snp	C/T	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669211	CTGGGCGCGGTGGCT[C/T]ACGCCTGTAATCCCA	10966
rs537882486	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82691805	TGCTGTGCCCCGACC[A/G]TATCCTGGGCCAGCC	10966
rs537966129	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82660319	GCACTCATGCACAGA[C/T]TCATACACAGGGCAC	10966
rs538155471	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82689095	AAAGGTTAAAAACAT[C/T]TCTGAATGTGAACAG	10966
rs538238037	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665604	GGATGCGGTGGCTGA[C/T]GCCTGTCATCCCAGC	10966
rs538259775	snp	G/T	0.00119737	0.0244387	intron-variant, downstream-variant-500B, utr-variant-5-prime	RAB40B, MIR4525	GRCh38.p7	17:82667945	ATGGGCGCTGACGGG[G/T]CACTGATGGGGCCTT	10966
rs538349853	in-del	-/ACAC	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82660290	ACACACGTACACATT[-/ACAC]ACACAAGCAGGCACT	10966
rs538393682	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82681940	TGGTAAAAAACAGAA[C/T]GCTTTCCCCATGAAA	10966
rs538491358	snp	C/T	0.00119737	0.0244387	downstream-variant-500B	RAB40B	GRCh38.p7	17:82656636	AGTTCAAGGATTCAG[C/T]CTTGTTGCCAGTGTC	10966
rs538520387	snp	C/G/T	0.00319074	0.0398324	intron-variant	RAB40B	GRCh38.p7	17:82686920	CATCCAGTGCTGGGG[C/G/T]GAAGGGTGCTCAGAG	10966
rs538529204	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82680924	AGTCCCAGCTACTCA[C/G]GAGGCTGAGGCAGGA	10966
rs538552505	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82689226	CCTGGGGCAGGAGGA[A/G]CAGTGAGCAGGTGCG	10966
rs538585597	snp	A/C			intron-variant	RAB40B	GRCh38.p7	17:82673083	GTGGTGGGCGCCTGT[A/C]GTCCCAGATACTTGG	10966
rs538601727	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82679502	TAGCCAGGATGGTCT[C/T]GATCTCCTGATCTTG	10966
rs538664802	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82680058	GGGGCTGGACATCTT[C/G]TGACCACAACTCCCA	10966
rs538665172	snp	C/T	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82674504	ATTAGCCGGGTGTGG[C/T]GGCGGGCACCTGTAG	10966
rs538717644	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82678695	GCCAAAAAGCAGACT[C/G]GCGGTCCCCGGGGCA	10966
rs538748381	snp	A/G	0.00478085	0.0486577	intron-variant	RAB40B	GRCh38.p7	17:82685748	CCCCCAAAGGCTCAC[A/G]TTCACCCAGAACTTC	10966
rs538758802	in-del	-/GCCTGGGCGTTGCAGCA	0.00199481	0.0315187	intron-variant	RAB40B	GRCh38.p7	17:82667342	CACATCTTCAGGCAG[-/GCCTGGGCGTTGCAGCA]GCTCTGGGCCTCTGT	10966
rs538767343	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82667556	TCCTGGACTCCAGAG[C/G]CTCTTTCTGTGGTGC	10966
rs538789167	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82682446	GAGACATACCATGTT[C/G]ATGATTGACAGAATC	10966
rs538909955	snp	C/T	3.3129e-05	0.00406982	synonymous-codon	RAB40B	GRCh38.p7	17:82658552	GATCCTGGCCAGCTC[C/T]GTGAACGACTCTGTG	10966
rs538912606	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82663654	CCCACGTCTGGGTCC[C/T]CCACCCGCAGGCCCG	10966
rs538923958	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82680779	GCTCACGCCTTTAAT[C/T]CCAGCACTTTGGAAG	10966
rs538974483	snp	A/G	0.00517822	0.0506191	intron-variant	RAB40B	GRCh38.p7	17:82659076	GGAAGTGGCCCTGCC[A/G]ACACCTTGGTTTTGG	10966
rs538994882	snp	C/T	0.0189856	0.0955633	intron-variant	RAB40B	GRCh38.p7	17:82664126	GGGGAGGGTGCTCCC[C/T]GGGGTGCTGTGCCGA	10966
rs539078382	snp	A/G/T	0.00279242	0.0372774	intron-variant	RAB40B	GRCh38.p7	17:82683050	CGGGAGGCTGAGGCA[A/G/T]GAGAATTGCTTGAAT	10966
rs539122455	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82694875	AGACCATGGGCAGAC[A/G]TTCTCAGACACAAAA	10966
rs539136684	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82687109	ATGCCCAGATCTGAT[A/G]ACGCTGGCCTCTATG	10966
rs539140144	snp	C/T	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82687198	CTCTCCTCAAACATA[C/T]GTGGCCTCCTGAGCT	10966
rs539197221	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668535	TCCCATGTTCAACAG[C/T]GCCCAGTCCCGAGGG	10966
rs539207015	snp	A/C	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82695294	CCTCCTGGGTTCCAG[A/C]GATTCTCCTGCCTCA	10966
rs539261078	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661164	GTCAGCAGCCACCAC[A/G]CCGCCAGCGTGAGAC	10966
rs539266009	snp	C/T	0.00159617	0.0282053	downstream-variant-500B	RAB40B	GRCh38.p7	17:82656857	CATCTCTACTAAAAA[C/T]ACAAAAATTAGCCGG	10966
rs539325004	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82659867	AAATGTCACGGTGAT[C/T]TGGGGACTAGAACTC	10966
rs539333543	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665076	GCTGCGTGGGATGCC[C/T]GCTCTCAGCTGTGTA	10966
rs539397767	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665578	AAAATAAAAAGCTAC[A/G]ATTAAGGGCTGGATG	10966
rs539397823	snp	A/G	0.00119737	0.0244387	intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660655	GGCACTCATGCAGAC[A/G]TATGCACAGTGCACG	10966
rs539471006	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82664409	GGATGGGTGCTCCCC[A/G]GGGCACTGTGCTGAC	10966
rs539496416	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666396	ATTACAGGCATACAC[C/T]GCCACGTCCAGCTAA	10966
rs539533747	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666978	AATTCTAAAGGGAAG[C/T]GCGCCGCTGAGAGGC	10966
rs539590151	snp	C/T	0.0193772	0.0965046	intron-variant	RAB40B	GRCh38.p7	17:82698197	GGCCTCGAGTGGAAC[C/T]GGGGGTGCAACAGGG	10966
rs539689603	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699200	GACGCGGCCGGAAGG[C/T]CCCCGCAGGCCGCCT	10966
rs539733233	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82679904	GGGGTGAACGCAGTC[A/G]TGGGAGGCTCACGAA	10966
rs539830986	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82658237	CTCCCAAGGCTCGGA[C/T]GCCCGTGGCCCTGGC	10966
rs539925289	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661927	AAGAAACAAATGAGG[A/G]TGGAAAGGGTGCTCC	10966
rs539991108	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82697152	CATCTCAGCTGCTCC[C/T]CCAAACTCTGCCCAT	10966
rs540055724	snp	A/G	0.00318978	0.0398085	intron-variant	RAB40B	GRCh38.p7	17:82697510	GGGTCTCTGTTGGAA[A/G]CGTGGGTTCAGCCCC	10966
rs540060939	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666285	ATTTCGCTCTTGTTG[C/T]CCAGGCTGGAGTGCA	10966
rs540097906	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82695064	GGCACTACAGCCACA[A/G]TACAGAAGCAAGGGC	10966
rs540129365	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82693198	TTTTAGTAGAGATGG[A/G]GTTTCACCAAGTTAG	10966
rs540147410	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82674067	ACAACCTGGCCAGGC[A/G]CGGTGGCTCGCGCCT	10966
rs540234304	snp	A/G	0.000399281	0.0141238			GRCh38.p7	17:82655003	ATTTATGTTTTTTGT[A/G]TATTCACCACCCAAA	10966
rs540254108	snp	A/G	1.66457e-05	0.00288489	intron-variant	RAB40B	GRCh38.p7	17:82664602	GAGGCTGCAGCTAAC[A/G]GGACGCTGGAAGTCT	10966
rs540315019	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82691102	ACCCCGGTGTGTCCA[C/T]GCACCGTGTAGTCTT	10966
rs540383934	in-del	-/AC	0.0150606	0.0854603	intron-variant	RAB40B	GRCh38.p7	17:82660556	CCTACACACACGTGT[-/AC]ACACACACACGCACA	10966
rs540390103	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82663438	CCCCCCATCCCCACC[A/G]CCCCAGAGCTGGAAC	10966
rs540443627	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668852	AGAGGCCCAGCCATG[C/T]CTCCGCTGCAGCCGG	10966
rs540711672	snp	G/T			intron-variant, downstream-variant-500B, utr-variant-5-prime	RAB40B, MIR4525	GRCh38.p7	17:82668053	AGACAAGTGGAGGGT[G/T]AGCGAGACGAGGAGG	10966
rs540718485	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669344	GCCGGGCGTGGTGGC[C/G]GGTGCCTGTAATCCC	10966
rs540721774	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82672016	TAACTCTAACACACA[A/C]ACACGCTCCCTGTAC	10966
rs540756002	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82663823	CAGACACCAGGCCAC[A/G]GGTTCTGATCCCAAA	10966
rs540855427	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82674935	ACCAGAATCCAGCCA[C/T]GCCTGAAACTACACC	10966
rs540860515	snp	A/C	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671003	CCTTTAAAATAACTT[A/C]TTTTGCTATGCATCT	10966
rs540920477	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82679744	GCAGGTCACCGAGCA[C/G]AGGGCAGGGGGCAGC	10966
rs540994053	snp	A/G	0.00358779	0.0422022	intron-variant, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82696605	TCCTCCAGGCGCTCA[A/G]TCTCCAGCCCTGTCC	10966
rs541004816	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699306	GCCCCATTTACGCGG[C/T]GTGCCTGAATGCCTG	10966
rs541036073	snp	C/T	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82678202	CTCTGTGTTACCTTA[C/T]GTTTTGGTCCACGAG	10966
rs541045561	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661995	GCCAGCGCTGTTTCC[C/T]GGAGTCTGCACATGC	10966
rs541207728	snp	A/C	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82688975	TGATAAAGTCTAGAT[A/C]TCTAATATTTTTATG	10966
rs541269674	snp	G/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82689304	CCACTCTGCACCACG[G/T]TGGTGCCTGGTGCCA	10966
rs541344301	snp	A/C	0.00159617	0.0282053	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82662424	ATCGTGAAGTGGGAG[A/C]ACTCCCTCCTCAGCT	10966
rs541405598	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82658299	CCCTCTGCCCACGTA[C/G]AGATCCCAGGAGCTC	10966
rs541431643	snp	C/T					GRCh38.p7	17:82656411	CCCTGGAGGTCTTTG[C/T]GGTCAGCCCTGCTCT	10966
rs541521710	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82677645	CACCTTCCAATCCTC[A/G]TCCACCACCCGTCTC	10966
rs541533976	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82686594	CAGGCCACAGAACGC[C/T]GAGGGCTGCCAGCAG	10966
rs541568782	snp	G/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82680382	GGCCGCTCGGGGGAC[G/T]GGACGGCAGTTCCCC	10966
rs541602716	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82691006	CTGATGCTCGTCTCC[A/G]GGAAGAAAAGCTCCC	10966
rs541738709	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82690671	AGCAGAGAGTGTGCA[C/T]GTGTGTGCAGGGGAA	10966
rs541845493	snp	G/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82675487	CCATACTTCAGAACT[G/T]GGGGTGGGGCAGGGT	10966
rs541915212	snp	A/G	0.00636936	0.0560724			GRCh38.p7	17:82656079	TCAGCCTCCTGAGTA[A/G]CTGGGATTACAGGTG	10966
rs541975002	snp	C/G	0.000724008	0.0190126	synonymous-codon, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698504	ATCCTGCAGGCTCGC[C/G]AGGATCTCGCCCTTG	10966
rs542054316	snp	A/G	0.000798403	0.0199641			GRCh38.p7	17:82655543	CCCTTCACCATCAGC[A/G]AGCTGGGAACGGAGG	10966
rs542090860	snp	A/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82664382	CGGGGGCGCTGTGCC[A/G]ATGGTGGTGGGGGAT	10966
rs542123648	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82696477	CTGGGCGTACACGTT[A/G]TTGGGTGCTTTATTC	10966
rs542152242	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82659976	CACCTGGATGGATTG[C/T]ACGCATACACGTGCA	10966
rs542157880	snp	G/T	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82676024	AGCACAGACGCTGCA[G/T]CCTGGGGCCTGGGAT	10966
rs542206975	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82667178	AGCTTCTGCCCCCTC[A/G]AAGGGTCTAGAACCC	10966
rs542265291	snp	A/C	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82697738	CTCGCCGGGCGCCGG[A/C]TTTCAAGCCTCAAAC	10966
rs542290170	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660818	TACTGATGAAGTCTT[G/T]CAAACAACCAACCAC	10966
rs542324497	snp	C/T	0.0023933	0.0345097	intron-variant	RAB40B	GRCh38.p7	17:82691887	GGAAAGAGCGTGAAC[C/T]GGGGACCCAGCTGCC	10966
rs542337384	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82663247	CTAGACGGGGCAGGC[A/G]TAGGAAGGGGACAGG	10966
rs542355148	snp	C/T	0.0023933	0.0345097	intron-variant	RAB40B	GRCh38.p7	17:82658844	CTCAGCATGGGACCT[C/T]GTTTGGAAAGACCGT	10966
rs542355471	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	RAB40B	GRCh38.p7	17:82656978	CAGATCGTGCCATTG[C/T]ACTCCACCCTGGGCA	10966
rs542360550	snp	C/T	0.00636936	0.0560724	intron-variant	RAB40B	GRCh38.p7	17:82692225	CAGAGCAGTGGGGCC[C/T]GCACGGTCCGTGGGC	10966
rs542399325	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82664725	CACAGGGGCCCTGCC[C/T]GCGCCCTCCCGCACC	10966
rs542446803	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82675451	ATCTATTCTGCTCCC[A/G]TGGATGGCACTCCCT	10966
rs542462484	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665259	ATGCCTTTCTTCTTC[C/T]TTTTTTTTTTTGAGA	10966
rs542554556	snp	C/T			utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657390	TGCACATAACCTCTA[C/T]ATCTGCAGCGTTTTA	10966
rs542611581	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82659151	GGACGCCCAGGTTGT[A/G]GTCGTCGGTTCTAGC	10966
rs542635208	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669246	TTTGGGAGGCCGAGC[A/G]GGGTGGATCACCTGA	10966
rs542654551	snp	C/T	0.00478085	0.0486577	intron-variant	RAB40B	GRCh38.p7	17:82685028	CTGAGGCAGGAGAAT[C/T]GCTTGAATCCAAAGG	10966
rs542684067	snp	C/T	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82690063	GACTTTCAGTTCAAA[C/T]TTGAAAGTGATGACT	10966
rs542700983	in-del	-/TTA	0.0197687	0.0974348	intron-variant	RAB40B	GRCh38.p7	17:82679257	AGGACACCACAAGCC[-/TTA]TTATTATTATTATTA	10966
rs542711196	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668348	CTGCAGGACTGGCAG[A/C]CCGGGCCCCAGGCCC	10966
rs542748362	snp	C/T	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82663699	GGCACCAGGACGCTC[C/T]GAGCTCCCTGCCGGG	10966
rs542754796	in-del	-/CACT			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82672068	TAACTCTAACACACA[-/CACT]CACATGCTCCCTGTA	10966
rs542759394	snp	A/G	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82694405	AGTGTGGTGGCAGGC[A/G]CCTGTAATCCCAGCT	10966
rs542766872	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82667168	GTTCTCAAGCAGCTT[C/T]TGCCCCCTCGAAGGG	10966
rs542799612	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82700000	AACAGAAGAGGGAGC[A/G]GAAGAAGAATTACAA	10966
rs542826469	snp	G/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82679066	TTTTTTGTATTTTTA[G/T]TAGAGACGGGGTTTC	10966
rs542941586	snp	G/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82673041	AAACCTCATCTCTAC[G/T]AAAAATACAAAAACT	10966
rs543078399	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82689691	AAGTAGAAAACTGGC[C/T]GGGCACGTGGCTCAC	10966
rs543103551	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82676658	TTTGAGATGGAGTCT[C/T]GCTGTGTCGCCCAGG	10966
rs543103657	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82670559	TTTTTTTTTGAGACG[A/G]AGTCTTACTCTGTCG	10966
rs543278451	snp	A/C	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82682804	GGAACAATTAGACAT[A/C]CCTGTGCAAAAGTAA	10966
rs543280681	snp	G/T	0.000399281	0.0141238	downstream-variant-500B	RAB40B	GRCh38.p7	17:82656890	GTGGTGGTGCACCTC[G/T]GTAATCCCAGCTACT	10966
rs543478771	snp	G/T			intron-variant	RAB40B	GRCh38.p7	17:82681520	CAACCCTGCAGCAAA[G/T]CATCTCAAGGCTCTG	10966
rs543540011	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82663077	GGGAGCAGGACAGGG[A/G]CTGACGGCAACCCCA	10966
rs543553630	snp	G/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82688917	CCAGCCTGAGCAACA[G/T]AGTAAGACTCTGTCT	10966
rs543597130	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82689156	CACTGTTGCCTCTGA[C/T]GCCCCTTGCCACTGT	10966
rs543658704	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82698742	CTGACAGCGCGCATC[C/T]CCGCCCGGCCCCGCC	10966
rs543659905	snp	A/G/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665314	CTGGAGTGCAGTGGC[A/G/T]TGATCACAGCTCACT	10966
rs543713529	snp	C/T	0.0023933	0.0345097	intron-variant	RAB40B	GRCh38.p7	17:82687013	TATCAAAGACCCTCC[C/T]GTCCAGTGCTGGGGG	10966
rs543718864	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699237	AGGAGTCCCTGTCGC[C/G]GTAGAATCCAGGCTC	10966
rs543720815	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82692709	TGTAGAGAACATTTT[C/T]TTTTTAAATCTGGGA	10966
rs543738157	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666435	TTTTTAGTAGAGATG[A/G]GGTTTCATCATATCA	10966
rs543802199	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661958	CCAGGGATCAGTTCC[C/T]AGAGGAGGCGGCCCT	10966
rs543813469	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82677105	AGGCGCCCGCCACCA[C/T]GCCCAGCTAATTTTT	10966
rs543937243	snp	G/T	0.000399281	0.0141238			GRCh38.p7	17:82655077	GTTTTTGTTCTGCCT[G/T]GGTTTGCTGTAGCAC	10966
rs543974025	snp	A/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82685953	GGATTACAGGTGCCC[A/G]CCACCACACCCAGCT	10966
rs544033515	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82688287	TGGGATTACAGGTGT[C/G]AGCCACCATGCCTGG	10966
rs544038557	in-del	-/TTAT/TTATTTAT	0.488222	0.10292	intron-variant	RAB40B	GRCh38.p7	17:82676959	TATTTATTTATTTAT[-/TTAT/TTATTTAT]TTTTTCTGAGACGGA	10966
rs544072354	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661536	GGGCTTGAGTTCTCA[C/G]ATGACGGCACACGCA	10966
rs544189945	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82689915	GAGGTTGCAGTGAAC[C/T]GAGATCGTGCCACTG	10966
rs544204516	snp	C/T	0.000399281	0.0141238			GRCh38.p7	17:82656380	CGTTCAACAGTGTGA[C/T]CAGGGAAGAGAGCGG	10966
rs544204771	snp	A/C	0.00478085	0.0486577	intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660755	CACGTACCTGCACAC[A/C]CGTGTACATGCACAC	10966
rs544250449	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82680268	ATACACCCAGGGGAG[C/T]GGCCATAGGATCCAG	10966
rs544306616	snp	A/C	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82690952	GCAAAGAGGAAGGAG[A/C]AAACCCCAGCAACTG	10966
rs544329116	snp	A/G	0.0023933	0.0345097	intron-variant	RAB40B	GRCh38.p7	17:82686667	GCCTGCCAAGGGAGC[A/G]TGGCCCAGGCAACAC	10966
rs544342206	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82660417	GCATGTACCTTCACA[C/T]ACGTGTAAACACACG	10966
rs544351315	snp	A/G	0.000399281	0.0141238			GRCh38.p7	17:82655433	ATTATCAGTAGTCCC[A/G]AGGAGACATCAATTA	10966
rs544431041	snp	G/T	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669438	CGAGATCACACCATT[G/T]CACTCCAGCCTGGGC	10966
rs544476456	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668763	AGCACAGAGACGCCC[A/G]CGTCTAGAGCTGCCC	10966
rs544493587	snp	A/C	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82663834	CCACAGGTTCTGATC[A/C]CAAAAGCCGATTCCC	10966
rs544583484	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82667625	ATCCTCCTCTGTCTC[C/T]TGCTAAACTCCACAC	10966
rs544604470	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82658349	AAGCTGTAGTCATTA[C/T]TTCTCTCAAATGCCT	10966
rs544606436	snp	A/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82663170	GGCCTGAAGCTGTGC[A/T]GCAGGAAGGGTCGGG	10966
rs544655071	snp	A/G	0.00398564	0.0444627	intron-variant	RAB40B	GRCh38.p7	17:82692011	AGAGCAGTGGGGCCC[A/G]CACGGTCCGTGGGCT	10966
rs544672988	snp	C/T	0.00159617	0.0282053	intron-variant	RAB40B	GRCh38.p7	17:82664676	GGTTTACAAGGCAGG[C/T]GGATGGGACCCCCTC	10966
rs544725439	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82694327	CTGAGGTTAGGGGTT[C/T]GAGACCACCCTGGCC	10966
rs544732388	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82697151	CCATCTCAGCTGCTC[C/T]CCCAAACTCTGCCCA	10966
rs544743100	snp	A/G	0.000399281	0.0141238	intron-variant, missense	RAB40B	GRCh38.p7	17:82662483	TGCCACCCTGAAGGA[A/G]CAGAGCAGAGCCCAA	10966
rs544757639	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82667135	CTCCTCTAAAAATGC[A/G]AGGCTGCGGAGGCCA	10966
rs544804953	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82670004	TTGGGAATCTATTTT[C/T]GAATGCGGAGATAAC	10966
rs544816890	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82659154	CGCCCAGGTTGTGGT[C/T]GTCGGTTCTAGCAGC	10966
rs544825546	in-del	-/A			intron-variant	RAB40B	GRCh38.p7	17:82687488	TTGCTGAGTCACATT[-/A]GGGGGAGGGTAATTA	10966
rs544874715	in-del	-/T	0.0513262	0.151752	intron-variant	RAB40B	GRCh38.p7	17:82695197	TTCTTTCTTTCTTTC[-/T]TTTTTTTTTTTTCGA	10966
rs544889433	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82678618	ATACAATGTACAGAC[A/G]TATTCATCTCTCAGC	10966
rs544893606	snp	G/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82672946	TGATGGTTCATGCCT[G/T]TAATCCCAGCACTTT	10966
rs544908322	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82674312	CCATTGCACTCCAGC[C/G]TGGGCAAAAAAGAGT	10966
rs544908888	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82675023	TGAGTTAATTTTCTT[A/G]TTTGCACCAAAATGT	10966
rs544940593	snp	A/T	0.00636936	0.0560724	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661465	GGAGTCAGCCCTTCC[A/T]GTGTGCCCCTAAGAG	10966
rs544975552	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82693820	AGGCGCAGTGGCTCA[C/T]GCCTGTAATTCCAGC	10966
rs545007236	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82700497	AGATGGCATTTAGTC[C/T]CCAGCCCCACCACTC	10966
rs545025480	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82674228	GCCTGTAATCCCAGC[C/T]ACTCAGGAGGCTGAG	10966
rs545036295	snp	A/C	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82689008	CAAGCCCTTTGGATG[A/C]TGTTGTTCTTTTCAG	10966
rs545077947	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82696070	AGACAGGGTTTCTCC[A/G]TGTTGATCAGGCTGG	10966
rs545085385	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668252	GGGTGGGGAAGTGCA[C/T]GCTGATTGGTCCACA	10966
rs545139891	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82677056	CGGGTTCAAGCAATT[C/T]TCCTGCCTCAGCCTC	10966
rs545143860	snp	C/T	0.437683	0.165152	intron-variant	RAB40B	GRCh38.p7	17:82672319	CTGTACTGACACACC[C/T]CACCCCTGTAACTCT	10966
rs545146959	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699913	GATAATGCCCCCACT[A/G]CTTCATCCCCTCCAC	10966
rs545162634	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82684972	TAGAAAAATTACCCG[A/G]GCGTGGTGGCAGGCG	10966
rs545177723	snp	C/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82677478	CTGCAGCGGCCAGCT[C/G]AACACACTCTGGCCC	10966
rs545224288	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82678221	TTGGTCCACGAGAAA[C/T]TAAGAAACATTTTTG	10966
rs545261195	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82658793	GTGGGTGCTCTGGGT[C/T]GAGGAACCCCCCACG	10966
rs545435222	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82683893	AGAGAATATGAGGAT[A/G]GTAGATGAGCACAGG	10966
rs545454348	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82673733	CTGAAACTGCACACC[C/T]TGTGGGCCTTGCTGT	10966
rs545473472	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82673754	GCCTTGCTGTAGGGA[C/T]CTTCGTGGCCAGGCT	10966
rs545488122	snp	A/C	0.0023933	0.0345097	intron-variant	RAB40B	GRCh38.p7	17:82682058	AACAAAAAGAAAGAA[A/C]AGGCATGCAGATTAA	10966
rs545561709	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82686635	GTCAGGGGAGTCAGG[A/G]AGGGTCCCCGCTTAG	10966
rs545569407	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82680801	CTTTGGAAGGCTGAG[A/G]CAGTTGCATCACAAG	10966
rs545573778	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82675640	AGAGCCAGTGTCTGA[C/T]GAGGGCTGCATCCTG	10966
rs545610219	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82685366	GTGCACTCAACTGAA[C/T]GCAGATTCCTGGGGC	10966
rs545621447	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82681210	GTGGTAAATGAGCTC[C/T]CCCACCCCCAACTCC	10966
rs545623320	snp	C/T	0.0023933	0.0345097	intron-variant	RAB40B	GRCh38.p7	17:82686998	CTCAGAGCTCAGGGG[C/T]ATCAAAGACCCTCCT	10966
rs545678296	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82660358	ACGCACGTGTACACA[C/G]ACACACGCACAGGCA	10966
rs545757470	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82689943	CTGCACTCCAGCCTG[C/G]GTGACAGAGCAAAAC	10966
rs545765797	snp	C/T	0.0023933	0.0345097			GRCh38.p7	17:82655718	TGCAGCGTGCCTGCA[C/T]GAGGCTGGCCACCCT	10966
rs545800237	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82670476	AGGCATGAGCCACCA[C/T]GCCCAGCCAAGGGCC	10966
rs545889786	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82684633	CTGACAAGTCAGATG[A/G]CTTCAGAGGCTCAGG	10966
rs545973712	snp	A/C/G/T	0.0100617	0.070217	utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698645	CTGCGGGGCTGAGCG[A/C/G/T]AGAGGCGGCGGCCCG	10966
rs546095122	snp	A/G			utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657483	ACTCTAAATTATCCC[A/G]CTGCCATTGCTTCTC	10966
rs546110883	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82697775	GATCCCCGGGCTGCC[C/T]GCCTGGGAGCTCTGG	10966
rs546242698	snp	C/T	9.11835e-05	0.00675155	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657740	TCACACGGAAGGCGT[C/T]GCACACATTCGCAAG	10966
rs546247805	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82683554	CCACTTTGGGAGGCC[A/G]AGGTAGGATGATCTC	10966
rs546355518	snp	A/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82690287	TTGTGTGTCCAGGGG[A/G]AGATCTGCAGAATTG	10966
rs546421488	snp	A/C	0.0023933	0.0345097	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661458	CTCACATGGAGTCAG[A/C]CCTTCCAGTGTGCCC	10966
rs546560349	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665792	GAATTGCTTGAACCC[A/G]GGAGGCGGAGGTTGC	10966
rs546587759	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82695779	TATCTTTTCTTAACT[C/G]TAAAACAAATATTTG	10966
rs546629678	snp	A/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82686049	ACTCGTGATCTGCCC[A/G]CCTTGGCCTCCCAAA	10966
rs546644515	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82685092	CACTCCAGCCTGGGT[A/G]ACAAGAGTGAAACTC	10966
rs546666343	snp	G/T	0.00318978	0.0398085	intron-variant	RAB40B	GRCh38.p7	17:82664297	CTCCCCGGGGTGCTG[G/T]GCTGATGGTGGTGGG	10966
rs546745196	snp	G/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668567	GCTGAGGTGGCAAGG[G/T]CTGGTGTGTCCGTGC	10966
rs546758482	snp	A/C/T	0.00199481	0.0315187	intron-variant	RAB40B	GRCh38.p7	17:82694523	GGCAACAGATTGAGA[A/C/T]TACATCTAAGAAAAA	10966
rs546795477	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82658905	CGCACTGAATTAGGG[C/T]CCTCATCTAATGACT	10966
rs546800996	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82689197	AATGCACCCAGCGCG[C/G]AGCAGCCTGCACTCC	10966
rs546818326	snp	A/G	0.000399281	0.0141238			GRCh38.p7	17:82654711	TGCACCACCATGCCC[A/G]GCTAGTGGTTTGTAT	10966
rs546858496	snp	A/G/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82684671	AGTGACCGGAGCCAG[A/G/T]TTCAAAGGCCTCCGG	10966
rs546913511	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82662766	GAGAGGGAGAAAAGT[A/G]TGAGGGTGACTGTTC	10966
rs546953271	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82698229	CGCCGCAGCACGAGG[A/G]CCAGGGCCGGGCGGA	10966
rs546956962	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82690757	AGTGTGCACGTGTGT[C/T]CAGGGGAAGATCTGC	10966
rs547062232	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82667711	AGAGCAAACTCCCCC[C/T]GTCAGAGGAGAGTGA	10966
rs547094804	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82695994	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA	10966
rs547100484	snp	C/G	4.9826e-05	0.00499104	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657806	ATCCACCAGCTGCCG[C/G]GGGTAACGCCGAGCT	10966
rs547169852	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82659497	TGGGTACCCATGAGC[C/T]CTGGAGGGCCCGGCC	10966
rs547196632	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82698808	TTTCACTGGCTTGGT[C/T]GTCCGTCCATCTTAC	10966
rs547224888	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665499	GTTCACACAATCTGC[C/T]CGGCTCAGCCTCCCA	10966
rs547263922	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82674325	GCCTGGGCAAAAAAG[A/G]GTGAAACTCCGTCTC	10966
rs547297435	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82670254	GCAGTGACGTGATCT[C/T]GCTCACTGCAACCTC	10966
rs547339343	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82676003	AGGACCCCACAGGGC[C/T]GGTAAAGCACAGACG	10966
rs547384637	snp	A/C	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82676279	CCCCCACACACAGTG[A/C]GGGCACCCCTCACCT	10966
rs547565098	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82672660	GCTGACGGGCTTGCG[C/T]GATGCCCTCTGCCAG	10966
rs547689749	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82683015	GGGCATGGTGGCACA[C/T]GCCTGTAATCCCAGG	10966
rs547691720	snp	A/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82688343	TTTTGGGCCGGGCAC[A/G]GTAGCTCACGCCTGT	10966
rs547703633	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82677150	GACGGGGTTTCACCA[C/T]GTTGGTCAGGCTGGT	10966
rs547740705	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82673128	AGAATCGCTTGAACC[C/T]GGCAGGCGGAGGTTG	10966
rs547782775	snp	C/T	0.0138799	0.0821421	intron-variant	RAB40B	GRCh38.p7	17:82674557	GGCAGGAGAATGGCG[C/T]GAACCCAGGAGGCGG	10966
rs547783930	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666919	ACTCTCGGCTGTGAT[C/T]GGATGTTGAGTGCTT	10966
rs547846011	snp	A/G	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82667268	CCTGTCGGGCAGAGC[A/G]AGGTGTGCAGTGGCG	10966
rs547846295	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82662144	ATGCACCTGTGGTCG[C/G]TGACCACCCTCAGCA	10966
rs547847152	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82675100	AACATCTGACACCCC[C/T]TAAACTGGGAAAAGC	10966
rs547912718	snp	G/T	0.00318978	0.0398085	intron-variant	RAB40B	GRCh38.p7	17:82664353	TGCCGACGGTGGTGG[G/T]GGGAGGGTGTTCCCG	10966
rs548056660	snp	A/C			intron-variant	RAB40B	GRCh38.p7	17:82692438	AGCAAGGACAAGATG[A/C]ATCTGACTGCCCTGG	10966
rs548081509	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82681690	AAATATACCAAATTC[A/G]GCAATCTATTATTGT	10966
rs548103634	in-del	-/G	0.0107246	0.0724382	intron-variant	RAB40B	GRCh38.p7	17:82697554	AGGTGGGCACAGGCT[-/G]GGGCTCCTTCCACAG	10966
rs548179067	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668953	ACCACAGTGGGGCAC[A/G]CGGCGTAGCCTCCAT	10966
rs548186294	snp	C/T	0.00318978	0.0398085	intron-variant	RAB40B	GRCh38.p7	17:82693258	GTGATCCATCCGCCT[C/T]GGCCTCTGAAAGTGC	10966
rs548207802	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82685627	CTCCAGTGCTGAAGC[C/T]CCAAGAAGAGGGGAC	10966
rs548239520	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669497	ATAAAAATAAAAAAT[A/T]AAAAAATTGGCCAAT	10966
rs548249179	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82674374	TGGTGGTTCACGCCT[A/G]TAACCCCAGCACTTT	10966
rs548285923	in-del	-/GG	0.0333695	0.124785	intron-variant	RAB40B	GRCh38.p7	17:82684113	TAATCCCAGCTACTC[-/GG]GGGAGGCTGAGGCAG	10966
rs548312247	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82674688	AGCAACCTAAAACAC[C/T]TGGGGAATGACTGAC	10966
rs548349383	snp	A/G	0.00438332	0.0466095	intron-variant	RAB40B	GRCh38.p7	17:82686009	GGGTTTCACCATGTT[A/G]GCCAGGCTGGTCTCA	10966
rs548397089	snp	C/T	0.000399281	0.0141238			GRCh38.p7	17:82655817	TGTCCCCGTGGCTGC[C/T]GTGCCCAGGTGGCCA	10966
rs548438135	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82686332	GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAA	10966
rs548448703	snp	A/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82674425	TCATGAGGTCAGGAG[A/T]TCGAGACCATCCTGG	10966
rs548488270	snp	C/T	0.000399281	0.0141238			GRCh38.p7	17:82654675	ATGCCTCAGCCTCCT[C/T]AGTAGCTGGGACTAT	10966
rs548489954	snp	G/T	0.0023933	0.0345097	intron-variant	RAB40B	GRCh38.p7	17:82697333	CTCTACCGAGCAGCC[G/T]CAGATCCCGCTTCCT	10966
rs548517246	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82660494	ACACGTGTACACATA[C/T]ACGCACATGCAGGCA	10966
rs548531510	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82664022	GGGGCGCTGTGCCAA[C/T]GGTGGTGGGGGAAGG	10966
rs548556591	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82688655	TAGTTTTGTTTGGGC[C/T]GGGCGTGGTGGCTCA	10966
rs548557696	snp	A/G	0.00159617	0.0282053	intron-variant	RAB40B	GRCh38.p7	17:82696298	AGTCACGCAGCAGAA[A/G]CATCCCCGAGCCTCC	10966
rs548599878	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82659767	CTTATTTTAACACAA[A/G]GTACATAATTTTGAT	10966
rs548658532	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82691668	GCCTGGGCGACAGAG[C/T]GAGACTCCATCTCAA	10966
rs548658695	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82686409	GAGCCACCGCGCCCG[C/G]CCAAGGGTCTTTTCA	10966
rs548686506	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82684619	AGCTCTTGGTGCACC[C/T]GACAAGTCAGATGGC	10966
rs548695471	snp	A/T			intron-variant	RAB40B	GRCh38.p7	17:82688534	GGCAGGAGAAGTGCT[A/T]GAAGCCGGGAGGCGG	10966
rs548719120	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82686809	CCAAAAGCCACTTCA[C/G]TCAGCAGCTCTGGAG	10966
rs548782157	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82691321	AGGCCCTCATGCTGG[C/G]GAAAAGGGTGGGAGG	10966
rs548863089	snp	C/T	0.000115614	0.0076022	synonymous-codon, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82664516	CTGCAGCTTCACCCG[C/T]CGCCCGTCCAGCAGG	10966
rs548863682	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82662094	ACCTCACGGATGAGC[A/G]GTGGGACGCGGCATG	10966
rs548883413	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82696817	TCTCCAGGGCAGCGC[A/T]GGCCCTCGGACTTTG	10966
rs548958622	snp	C/T	0.00318978	0.0398085	intron-variant	RAB40B	GRCh38.p7	17:82689727	TAATCCCAGCACTTT[C/T]GGAGGCCAAGGCGGG	10966
rs549039099	snp	A/G	0.00279162	0.0372561	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699511	TGCACATGTATGTGC[A/G]TGTGCATGTGTCCCT	10966
rs549053960	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82688572	AGTGAGCTAAGAACA[C/T]GCCACAGCACTCCAG	10966
rs549054077	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82693853	TTTGGGAGGCCGAGG[C/T]GGGCAGATCACCTTA	10966
rs549065274	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82658995	AGAGGCTGGAGCGGT[A/G]CAGCCACAAGCCAGG	10966
rs549077803	snp	A/G			intron-variant, downstream-variant-500B, synonymous-codon	RAB40B, MIR4525	GRCh38.p7	17:82667889	TTGCCACCGAGCCCA[A/G]CAGGCACGCTGAGTG	10966
rs549082237	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82683959	GGCGCAGCGGCTAAC[A/G]CCTGTAATCCCAGCA	10966
rs549115389	snp	A/G	0.0023933	0.0345097	intron-variant	RAB40B	GRCh38.p7	17:82689176	CTTGCCACTGTCTTC[A/G]CTCCAAATGCACCCA	10966
rs549190836	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82693475	CTGGTGGGAGCACCA[A/G]GTGAAAAATGCTTTG	10966
rs549254001	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661747	CAAAAATTAGCTGGA[C/G]ATGGTGGTGTGCTCC	10966
rs549255833	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665731	AATTAGCCGGGTGTG[A/G]TGGCGGGCTCCTGGA	10966
rs549273260	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82673406	ATCTGGACTGGGAGG[A/G]CTGTTGCCCTGGGGC	10966
rs549376679	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82659326	AAACCTGACCCCACG[C/G]ATAGCCGAGGTACGC	10966
rs549465368	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665386	GTCCCCTGAGTAGCC[A/G]GGACTACGGGCATGT	10966
rs549684028	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669765	TTACGCTTTGAGCGA[C/T]GACCAAAAATCTCTT	10966
rs549755861	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660574	CACACACACGCACAG[A/G]CACTCATGCCCAGAT	10966
rs549822560	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	RAB40B	GRCh38.p7	17:82656665	TCGTGTATTAGCTCC[A/G]ATATGTGATGTCTAC	10966
rs549983530	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82670176	CCTTGAGGGCCAACA[A/G]TCTTTTTTTTTTTTT	10966
rs550014728	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82692352	CGAGAGGAAGACAAA[C/T]GCCCAGGAGGGAGAA	10966
rs550064013	snp	A/G					GRCh38.p7	17:82656226	GCTGGGATTACAGGT[A/G]TGAGCCATCACACCC	10966
rs550081582	snp	C/T	0.00517822	0.0506191			GRCh38.p7	17:82655373	ACCTCCAAAGAGCTC[C/T]GAGTCACAAAGCCTT	10966
rs550157352	snp	A/T			intron-variant	RAB40B	GRCh38.p7	17:82697039	CGCAGGCTCCCCTCC[A/T]GCCCCACGGAGCACA	10966
rs550173193	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671198	CACACCCCACCCCCG[C/T]AACTCTAACACACAC	10966
rs550215990	in-del	-/CA			intron-variant	RAB40B	GRCh38.p7	17:82682124	ACACACACGCATGCA[-/CA]CACACACACACACAG	10966
rs550234325	snp	C/T	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82672650	AGACACCTGAGCTGA[C/T]GGGCTTGCGCGATGC	10966
rs550309764	snp	A/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82676926	CTACCGCGCCCGGCC[A/G]GTAGCCTACTAATTT	10966
rs550335108	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82682466	TTGACAGAATCAGTA[C/T]TGTTAAGATGACAAG	10966
rs550413185	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82694589	TGGAAACTCAAAGAG[C/T]ACGTTCATACTAAAA	10966
rs550446544	snp	C/G/T	0.00239369	0.0345212	intron-variant	RAB40B	GRCh38.p7	17:82676444	ACAGCCTCTCCCCCC[C/G/T]CACACAGGGCACCCC	10966
rs550446695	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82676180	GCTGCCAGCAGTCCA[C/T]GTCAGCTCAGCAAAG	10966
rs550465503	in-del	-/CCT			intron-variant	RAB40B	GRCh38.p7	17:82687008	AGGGGTATCAAAGAC[-/CCT]CCTGTCCAGTGCTGG	10966
rs550476184	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657263	TCTTGTACAAAAAAC[A/T]GTAGATTTACAGAAA	10966
rs550488247	snp	A/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82685194	TCAATAAAAGCAGAG[A/G]GGAAGCGGGAGAGGA	10966
rs550559971	snp	C/T	0.00199481	0.0315187	intron-variant	RAB40B	GRCh38.p7	17:82674365	GACCAGGCGTGGTGG[C/T]TCACGCCTGTAACCC	10966
rs550623806	snp	C/T	0.0189856	0.0955633	intron-variant	RAB40B	GRCh38.p7	17:82674632	CGACAGAGCAAGACT[C/T]GTCTTAAAAAAAAAA	10966
rs550640936	snp	C/G	0.000399281	0.0141238			GRCh38.p7	17:82655294	CATGTTCCGCTTCTG[C/G]GGACTTCTGGTGGTG	10966
rs550673231	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82684326	ACTGAAACACTCACA[C/T]ACTGCTGACGGGGAT	10966
rs550697426	snp	G/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82679163	GCTGGGATGACAGGC[G/T]TGAACCACTGAGCAG	10966
rs550698972	snp	A/G	0.00358779	0.0422022	intron-variant	RAB40B	GRCh38.p7	17:82697192	CGTCCCCTAAGCTGA[A/G]GTGTGGCCGGGCACC	10966
rs550753694	snp	A/G	0.000399281	0.0141238			GRCh38.p7	17:82654535	CGAGTTCAGCACTGC[A/G]GCAGGGTAGGGACAG	10966
rs550790367	snp	A/C	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82685612	CAACAGGGCCAGGGG[A/C]TCCAGTGCTGAAGCT	10966
rs550825201	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82692932	ACACTCCTAGCAAGC[A/G]TTGAAAGAAATTCAA	10966
rs550843469	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82678698	AAAAAGCAGACTGGC[C/G]GTCCCCGGGGCAGAG	10966
rs550846964	in-del	-/AGGA	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82681395	GAAGTCTCCTAATAC[-/AGGA]AGGAAGCAGTAGTTA	10966
rs550874293	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82658954	GAAGACACAGACACT[C/T]GGAGGAGGCCATGTT	10966
rs550938348	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82686396	GGATTATAGGCATGA[A/G]CCACCGCGCCCGGCC	10966
rs550981843	snp	G/T	0.0729998	0.176553	intron-variant	RAB40B	GRCh38.p7	17:82664136	CTCCCTGGGGTGCTG[G/T]GCCGATGGTGGTGGT	10966
rs550990152	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82674369	AGGCGTGGTGGTTCA[C/T]GCCTGTAACCCCAGC	10966
rs551108074	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82664320	GTGGTGGGGCTGGTG[A/G]TGCTCCCCGGGGTGC	10966
rs551237297	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665983	TAGTACAGTAGCACA[A/G]TCACAGCTGACTGCA	10966
rs551245807	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668866	GCCTCCGCTGCAGCC[A/G]GCATCTTGGCAGCAG	10966
rs551254672	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82670873	ACGAGTTTCAAAACC[A/G]TCTTTCGTTTCTGTT	10966
rs551478775	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82687930	TAAAATAATTAGCCG[A/G]GCATGGTGGCATGCA	10966
rs551524906	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82677677	AGGGCCAGCACCCAA[C/G]CGTTTGGGGTTTCCA	10966
rs551569130	in-del	-/ACACAC	0.0900242	0.192114	intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660690	TGCACACACATGTAC[-/ACACAC]ACACACACACAGGCA	10966
rs551659908	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82684475	AGTTCGCACAAAAAC[A/G]AGTCATAAACATGCA	10966
rs551713678	snp	A/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82673205	TGAGACTCTTGTCTC[A/T]AAAAAAAAATTGCCT	10966
rs551755255	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82662858	GGAGCTGGGAGAGGG[C/T]ACGCGCCAGCCCTGA	10966
rs551816794	snp	C/T	1.66532e-05	0.00288554	synonymous-codon	RAB40B	GRCh38.p7	17:82658606	GACCTCAAAGAAGGT[C/T]ACGCCCAGGCGCTCG	10966
rs551816819	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82663482	CCCATCCCAAGCCAA[A/G]AGCGGGTGGAGGGAG	10966
rs551842677	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, missense	RAB40B, MIR4525	GRCh38.p7	17:82670067	GGACACTCACCCCCA[C/T]GGGCTGAGAGGCTCA	10966
rs551916334	snp	G/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82672770	CATTTATTTTCTTTA[G/T]AAATTACCCAGTTTG	10966
rs551918939	snp	A/G	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82680500	TGCTTCTGAAGTTAA[A/G]AAAAATATCGCATAT	10966
rs552057609	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82686337	GGCTGGTCTCGAACT[C/T]CTGACCTCAAGTGAT	10966
rs552057709	snp	A/T	0.00676609	0.0577691	intron-variant	RAB40B	GRCh38.p7	17:82679974	GTGGCTGTGGGAGGG[A/T]CAGAGGGGCCAGATC	10966
rs552154179	snp	G/T	1.65258e-05	0.00287448	missense, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82664554	TCGTCTTGTAGTCGA[G/T]GCCTGCGGAAGGGTT	10966
rs552299972	snp	A/G			utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657517	TTCCATTGAATTTAT[A/G]CTAATCACTCCAATA	10966
rs552379314	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82675127	AAGCTACAAAGGATG[C/G]ATTTTCACATCTTCC	10966
rs552491666	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669216	CGCGGTGGCTCACGC[C/T]TGTAATCCCAGCACT	10966
rs552496882	snp	C/T	0.00159617	0.0282053	downstream-variant-500B	RAB40B	GRCh38.p7	17:82657045	AATAAATACAAAATT[C/T]GAAAGAACCGGTCGC	10966
rs552523309	snp	A/G	0.00159617	0.0282053	intron-variant	RAB40B	GRCh38.p7	17:82679695	ACGCCAACCCTGTGC[A/G]GCCACTGCTGCCCCG	10966
rs552569122	snp	A/C	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82676434	CTCACCTTCAACAGC[A/C]TCTCCCCCCCCACAC	10966
rs552633676	snp	A/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82676904	GTGCTGGGATTATAG[A/G]CGTGAGCTACCGCGC	10966
rs552644629	snp	G/T			intron-variant	RAB40B	GRCh38.p7	17:82697305	GAGCTGCCCTTAGGG[G/T]ACAGCCTGCACCCTC	10966
rs552705423	snp	A/C	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82682393	TAAAAGCTACAAACC[A/C]CTAATAAAAGGAATC	10966
rs552705573	snp	C/G	0.00914312	0.0669923	intron-variant	RAB40B	GRCh38.p7	17:82677718	GCCTGGCCCTACACA[C/G]AGCCCGCATCCTCTT	10966
rs552871327	snp	A/G	0.000798403	0.0199641			GRCh38.p7	17:82656494	TCGGAGCTCCTCACC[A/G]AGGCTCAGGAGCACG	10966
rs552895291	snp	C/T			intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661346	GCTTTAAAAAACTTG[C/T]TGAATCTGAAGATAA	10966
rs552927085	snp	G/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82685696	AACGAAACTGTCCTT[G/T]CGGGTTTCACCATCT	10966
rs552943050	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699837	CTCACCAGGTGCACA[C/T]TGGTTTATTTGGTGC	10966
rs552990105	snp	A/G	0.00755907	0.0610114	intron-variant	RAB40B	GRCh38.p7	17:82679427	GCTGGGACTACAGGT[A/G]CCTGCCACCACGCCC	10966
rs553036472	snp	A/G			utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657576	AAGGAAAAAGTTGCA[A/G]TGCAATCATGATAAA	10966
rs553036734	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82677829	GTGCTGCACCTGCCC[A/G]ACCCCTGCACCTGAC	10966
rs553102871	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82663643	GTCCTCACCTCCCCA[C/T]GTCTGGGTCCTCCAC	10966
rs553108626	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82677052	CTCCCGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG	10966
rs553129984	snp	A/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82674199	TACAAAATTAGCCGG[A/G]TGTGGTGGCGGGTGC	10966
rs553149769	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82689312	CACCACGGTGGTGCC[C/T]GGTGCCAGGCTGGTG	10966
rs553183308	snp	C/G	0.00358779	0.0422022	intron-variant	RAB40B	GRCh38.p7	17:82684092	TGGGTGTGGTGGCAG[C/G]CACCTGTAATCCCAG	10966
rs553231064	snp	A/C	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82658231	CCCGCCCTCCCAAGG[A/C]TCGGACGCCCGTGGC	10966
rs553239847	snp	C/T	0.00358779	0.0422022	intron-variant	RAB40B	GRCh38.p7	17:82663094	TGACGGCAACCCCAA[C/T]GCCAGCCCAGCGAGG	10966
rs553318573	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82683527	ACATAGTGGCTCACA[A/G]CTGTAATCCCACCAC	10966
rs553466806	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82686960	ATGGAAGACCCTCCC[A/G]TCCAGTGCTGGGGGG	10966
rs553523863	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665065	ACAGACGTGACGCTG[C/T]GTGGGATGCCCGCTC	10966
rs553529440	snp	A/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82694969	AGAGGGACAGCACAA[A/T]GAACAGAGACATAAA	10966
rs553530870	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82682552	CTTGGTAGAAATCAA[C/G]AAAGCCAACATTTAA	10966
rs553548183	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82691525	ACCCCCATCTCTACT[A/G]AAAATACAAAAATTA	10966
rs553585972	snp	A/T	0.000399281	0.0141238	downstream-variant-500B	RAB40B	GRCh38.p7	17:82656713	TGAAGTAAAGGGCTA[A/T]AAGAAATACACAAAA	10966
rs553611661	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82693393	AAAGGCAAACTACAC[A/G]CCACAGAAGGACAGA	10966
rs553660002	snp	C/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82683788	CCAGCCTGGGCAACA[C/G]AGCAAGACCCTGTTT	10966
rs553681262	snp	G/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82697533	TCAGCCCCGAGGCGC[G/T]GCAGGAAGGTGGGCA	10966
rs553718267	snp	A/G	0.00119737	0.0244387	intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660635	CGTGCACACACACAC[A/G]CACAGGCACTCATGC	10966
rs553832610	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661815	TTGTTTGAGCCCGGC[A/G]GGCGGAGGTTGCAGT	10966
rs553904635	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82660341	ACAGGGCACGTACCT[A/G]CACGCACGTGTACAC	10966
rs554011117	snp	G/T	0.00159617	0.0282053	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699161	TGCCTGGCCGGGTGG[G/T]GCTCGGGGTCGGTCC	10966
rs554086386	snp	A/G/T	0.00309408	0.0392122	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657711	TCGAAGTCCGACGGG[A/G/T]TAGTGTGTTTCCATC	10966
rs554229678	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661406	CCAGGGGAGAGAGGC[C/T]GGTGGGATCCCTGCT	10966
rs554240549	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82659157	CCAGGTTGTGGTCGT[C/T]GGTTCTAGCAGCCCC	10966
rs554297612	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666170	GCTGGTCAACCTCCT[A/G]GACTCAAGTGATCCT	10966
rs554373269	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82670860	TTTTAAGCGCCCTAC[A/G]AGTTTCAAAACCATC	10966
rs554377924	snp	G/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82663702	ACCAGGACGCTCCGA[G/T]CTCCCTGCCGGGTGC	10966
rs554434588	snp	C/G	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671270	ACCCTAACACACACA[C/G]TCACACATCCTGTAC	10966
rs554509156	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669309	GGAGAAACCTTGTCT[C/G]TGCTAAAAATACGAA	10966
rs554544149	snp	C/G	0.00199481	0.0315187	intron-variant	RAB40B	GRCh38.p7	17:82695515	TTCAATAACAAGCAC[C/G]TATAGTGTTTCTCAG	10966
rs554572239	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82664384	GGGGCGCTGTGCCGA[C/T]GGTGGTGGGGGATGG	10966
rs554649209	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82675380	CAGCCGCCTGTCTGA[C/T]GTGGTCTCCACCAAG	10966
rs554672230	snp	G/T			intron-variant	RAB40B	GRCh38.p7	17:82688510	ATCCCAGCTACTCAG[G/T]AGGCTTGAGGCAGGA	10966
rs554727409	in-del	-/GCAGAGGTT	0.0205511	0.0992634	intron-variant	RAB40B	GRCh38.p7	17:82680959	ATTTGAACCCGGGAG[-/GCAGAGGTT]GCAGTGAGCTGAGAT	10966
rs554849998	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B, utr-variant-5-prime	RAB40B, MIR4525	GRCh38.p7	17:82668137	CTCTGCAGGCAGGTC[A/G]TCCTGACAAGTGTTC	10966
rs554925869	snp	C/G	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671654	ACACACACACTCACA[C/G]CCTGTACTCACTGAC	10966
rs554990162	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82672826	ATGACACCAGGTAGA[C/T]GCCATCCACAGCTGA	10966
rs554990645	snp	C/T			intron-variant, upstream-variant-2KB, missense	RAB40B, MIR4525	GRCh38.p7	17:82670064	AAGGGACACTCACCC[C/T]CACGGGCTGAGAGGC	10966
rs554994920	snp	C/T	0.000265728	0.0115236	missense	RAB40B	GRCh38.p7	17:82658516	CCGCCAGAGCCGGTC[C/T]ATCCCATGCCGCAGC	10966
rs555061630	snp	A/C	0.00318978	0.0398085	intron-variant	RAB40B	GRCh38.p7	17:82677035	CTCACCGCAAGCTCC[A/C]CCTCCCGGGTTCAAG	10966
rs555079030	snp	A/C	0.000911531	0.0213292	missense	RAB40B	GRCh38.p7	17:82658639	GTAGGCCTGGGCCTG[A/C]TCCGTGGGCACCTGC	10966
rs555127540	snp	A/C	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82683237	TTTCTAGAAGAAAAT[A/C]TTTGTGACTTTGGGT	10966
rs555181624	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82686174	TGGAGTGCAGTGGCA[C/T]GATCTCAGCTCACTG	10966
rs555187112	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82680135	AGACCGGAGGCCTGG[C/T]AGGGTTCGAGGGCTC	10966
rs555239163	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657538	CACTCCAATATCACC[A/G]TTCTTACAAAAGCAG	10966
rs555320327	snp	G/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82685896	GCAACCTCCACCTCC[G/T]GGATTCAAACGATTC	10966
rs555389632	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666468	CAGGCTGGTCTTGAA[C/T]TCCTGACTTCAGGTG	10966
rs555409447	snp	A/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82694022	TGGGAGGCAGAGGTT[A/G]CAGTGAGCTGAGATC	10966
rs555471495	snp	G/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82689296	AGCTGCGTCCACTCT[G/T]CACCACGGTGGTGCC	10966
rs555472052	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82684797	CTTGACCGTGATGGC[A/G]GTCACACCACTGTCT	10966
rs555532117	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82682820	CCTGTGCAAAAGTAA[C/T]GAATCTCAATCTATA	10966
rs555730207	snp	G/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82693015	TATTTTTTTTCTTTT[G/T]TTTTGGAGACAGAGT	10966
rs555819313	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699785	GCTCTAGAGAGCAAG[G/T]GTTGCCAGGCCGAGG	10966
rs555825061	snp	A/G	5.24269e-05	0.00511964	synonymous-codon	RAB40B	GRCh38.p7	17:82658705	GATCTTGGGGACTCC[A/G]GGGGCATGCTAGCGG	10966
rs555838821	snp	A/G			upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699505	GGTGTCTGCACATGT[A/G]TGTGCGTGTGCATGT	10966
rs555868761	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82691483	CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGACC	10966
rs555944269	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82696471	ATTCGTCTGGGCGTA[A/C]ACGTTGTTGGGTGCT	10966
rs555978991	snp	A/G	0.00159617	0.0282053	intron-variant	RAB40B	GRCh38.p7	17:82677026	CGATCTCGGCTCACC[A/G]CAAGCTCCACCTCCC	10966
rs555997566	in-del	-/TTT	0.00119737	0.0244387			GRCh38.p7	17:82656116	GCCATGCCAAGCCAA[-/TTT]TTGTAATTTTATTAG	10966
rs556040361	snp	A/T			intron-variant	RAB40B	GRCh38.p7	17:82678434	AAAAAACAAGAACAA[A/T]AAAGGGAGAAGTCAA	10966
rs556119021	snp	A/G	1.65384e-05	0.00287557	intron-variant	RAB40B	GRCh38.p7	17:82664561	GTAGTCGATGCCTGC[A/G]GAAGGGTTAGAGACG	10966
rs556120388	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82686546	GAGAAGGCTGTGTGA[C/T]GACAGACAGCAGGGA	10966
rs556123282	in-del	-/C	0.00279162	0.0372561	intron-variant	RAB40B	GRCh38.p7	17:82686824	TCAGCAGCTCTGGAG[-/C]CCCCCCACCTTCCTC	10966
rs556254084	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665621	CCTGTCATCCCAGCA[C/T]TTTGGGAGGCTGAGG	10966
rs556287926	snp	A/G	0.000399281	0.0141238			GRCh38.p7	17:82655476	AAGGAAGGAAGAGAA[A/G]AATACAGGTTTGGCC	10966
rs556289953	snp	G/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82660320	CACTCATGCACAGAC[G/T]CATACACAGGGCACG	10966
rs556294486	snp	G/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82664378	TTCCCGGGGGCGCTG[G/T]GCCGATGGTGGTGGG	10966
rs556298699	snp	C/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82695607	CTCAGCATTTGAGGA[C/G]GCCAAAAAAGGAGGA	10966
rs556313632	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661287	TAGAAAAAATAGTGA[C/T]GGTTTTAACATAATT	10966
rs556426569	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82659940	GCAGTAATCGCCACC[C/T]CTCGAGGAGTGTGGC	10966
rs556490794	snp	C/T	0.00119737	0.0244387	intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660768	ACACGTGTACATGCA[C/T]ACACAGTCCCGTAAA	10966
rs556511437	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82663187	CAGGAAGGGTCGGGG[C/T]GCTTGGGGACACTGT	10966
rs556601845	snp	C/T	0.00993419	0.0697739	intron-variant	RAB40B	GRCh38.p7	17:82698326	CCCGGCCACGCGCCC[C/T]GGCCTCTTCCCGACC	10966
rs556717963	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82692582	ACAACGGTGGCCGTG[C/T]GATGCGGGGTGGGGG	10966
rs556766541	snp	A/G	0.000798403	0.0199641			GRCh38.p7	17:82655988	GGAGTTTCACTTGTC[A/G]CCCAGGCTGGGGTGC	10966
rs556774760	snp	G/T	0.0023933	0.0345097	intron-variant	RAB40B	GRCh38.p7	17:82680927	CCCAGCTACTCAGGA[G/T]GCTGAGGCAGGAGAA	10966
rs556781457	snp	C/T	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82674757	TGGCATCGCAGGCAA[C/T]GTTCGTATGGTTTGG	10966
rs556844980	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82670310	GTGCCTCAGCGTCCC[A/G]TGTAGCTGGAATTAC	10966
rs556889149	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B, utr-variant-5-prime	RAB40B, MIR4525	GRCh38.p7	17:82668035	AGGAAGAATGAGGTA[C/T]CCAGACAAGTGGAGG	10966
rs556923650	snp	A/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82674505	TTAGCCGGGTGTGGT[A/G]GCGGGCACCTGTAGT	10966
rs556950646	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82663681	CCCGACCACAGCCCC[A/G]CTGGCACCAGGACGC	10966
rs556984997	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82674871	GTGTGCAGGGAGTAG[A/G]CAGAGGAGAAAGAAC	10966
rs557087051	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82659424	ATCCAGTGTTGTGCC[A/G]AGGTGAGGCACCCTC	10966
rs557095492	snp	C/T			intron-variant, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82664894	CGCTGGGTGTGCCCC[C/T]GTCTGGGCTGGTCCT	10966
rs557102095	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82674070	ACCTGGCCAGGCGCG[A/G]TGGCTCGCGCCTGTA	10966
rs557124943	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668778	GCGTCTAGAGCTGCC[C/T]CAGGGCAGCGGGCCG	10966
rs557134007	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82678674	GTTGAGTTAAAACAC[C/T]GGAAAGCCAAAAAGC	10966
rs557179624	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82677980	AGATAAACCCTCTAA[C/T]GCAGCCATGTCTGCC	10966
rs557197277	snp	A/G			intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660885	TACGTAAGCTTAACC[A/G]CCTTGTCCTCCAATC	10966
rs557246008	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82684725	GGAGGTGGGGTTGGG[A/G]AGGGGCTGCCTACAA	10966
rs557295493	in-del	-/T			intron-variant	RAB40B	GRCh38.p7	17:82672937	TACCAGGCGTGATGG[-/T]TCATGCCTGTAATCC	10966
rs557316221	snp	C/G	0.00199481	0.0315187	intron-variant	RAB40B	GRCh38.p7	17:82676600	CCGCCAGTTTGACAT[C/G]TCTGCTTCAGTGGCC	10966
rs557521736	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82690365	ACGTGTGTCCAGGGG[A/G]AGATCTGCAGAATTG	10966
rs557531380	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82687235	AACAGACTTTATTTC[C/T]AGATGAATTTTATTA	10966
rs557624478	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660740	CACGCATACACAGTG[C/T]ACGTACCTGCACACA	10966
rs557654684	snp	C/T	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82695013	TTGGTGAGCACTGAC[C/T]GTATTTAAATGTTGA	10966
rs557713905	snp	C/T	0	0	intron-variant	RAB40B	GRCh38.p7	17:82695301	GGTTCCAGCGATTCT[C/T]CTGCCTCAGCCTCCC	10966
rs557857673	snp	C/T	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82693620	TGGCAGAACAAACCA[C/T]AATAGTCAGAAACCT	10966
rs557929915	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699213	GGCCCCCGCAGGCCG[C/T]CTCGCCGGAGGAGTC	10966
rs557932004	snp	C/G	0.00199481	0.0315187	intron-variant	RAB40B	GRCh38.p7	17:82687001	AGAGCTCAGGGGTAT[C/G]AAAGACCCTCCTGTC	10966
rs557970543	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669065	GAAAATAGCCAGGCA[C/T]GGTGGCTCACGCCTG	10966
rs558034680	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666316	GTGGTGCAATCTTGG[C/G]TCACTGCAACCTCGG	10966
rs558047639	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82697570	GGGCTCCTTCCACAG[C/T]CTCAGGGTCGGCCTC	10966
rs558110872	snp	G/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82698202	CGAGTGGAACTGGGG[G/T]TGCAACAGGGACGCC	10966
rs558198270	snp	A/G	0.00159617	0.0282053	intron-variant	RAB40B	GRCh38.p7	17:82693152	GGAATACAGGTGCCC[A/G]CCACCACACCTGGCT	10966
rs558261462	snp	C/T	0.00636936	0.0560724	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82662093	AACCTCACGGATGAG[C/T]GGTGGGACGCGGCAT	10966
rs558274656	snp	C/T	0.00199481	0.0315187	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82662257	GAGAAGCAAATTGAT[C/T]TAGAATTCAAGCCTC	10966
rs558276548	snp	C/G	4.94189e-05	0.00497062	missense	RAB40B	GRCh38.p7	17:82658009	TCATCCTGGCATTCA[C/G]GCCGTTGGCCATCGA	10966
rs558372652	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82689196	AAATGCACCCAGCGC[A/G]GAGCAGCCTGCACTC	10966
rs558418843	snp	C/G	0.00159617	0.0282053	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661939	AGGGTGGAAAGGGTG[C/G]TCCCCAGGGATCAGT	10966
rs558524309	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82690901	CCGGGGGAGCATGGA[A/G]TGGGCACGCATGTCC	10966
rs558547347	in-del	-/G	0.00160385	0.0282728	intron-variant	RAB40B	GRCh38.p7	17:82675823	TCAGCACCCGAATTT[-/G]GGGGGGTCACAAACA	10966
rs558558832	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665110	GTGCATGTGAACCAC[A/G]CATGTGCAGGGACAC	10966
rs558655809	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82696398	ACTCACCTTCAATCA[A/G]ACTCAACACTGTCAA	10966
rs558673209	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82664367	GTGGGAGGGTGTTCC[C/T]GGGGGCGCTGTGCCG	10966
rs558682136	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668695	GGCCAGGCATTTGGA[A/G]CAGGCACTTCTAAGC	10966
rs558698055	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82678648	CCCAGCTTTTGAGAA[A/G]TCTGTCTTATGTTGA	10966
rs558751297	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82678385	TCACTGAGTGAGTCA[A/G]AAAACAGGGACAAAA	10966
rs558887103	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82662019	CACATGCAACGAACA[C/T]ACCTACATCAATGGG	10966
rs558948672	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82662428	TGAAGTGGGAGCACT[C/G]CCTCCTCAGCTGGGA	10966
rs559028304	snp	A/G	0.00358779	0.0422022	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661618	AAGGCCGGGCTTGGC[A/G]GCTCACACCGATAAT	10966
rs559028580	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666582	AATATGTTTCCCCGC[C/T]CCCATCACCCCCCAG	10966
rs559097850	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82693302	GTGAGCCACCAGGCC[C/T]GGCCGACTTGGGCAT	10966
rs559099193	snp	C/G					GRCh38.p7	17:82656155	GGTTTCATCACGTTG[C/G]CCAGACTGGTCTTGA	10966
rs559147199	snp	C/G/T			intron-variant	RAB40B	GRCh38.p7	17:82684666	TGCTGAGTGACCGGA[C/G/T]CCAGGTTCAAAGGCC	10966
rs559258578	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671113	AGATGAAAATGTAGC[G/T]CTCGGTCACTGACAC	10966
rs559306437	snp	A/C	0.00358779	0.0422022	intron-variant	RAB40B	GRCh38.p7	17:82680205	TGTCACGGAGGTCTC[A/C]TGCAGCCTTGGACCC	10966
rs559372298	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82684866	CGCCTGTAATCCTAG[A/G]ACTCTGGGAGGTCGA	10966
rs559377117	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82698855	GGGCTGTCGCCCACC[A/C]GCCCCTCCTGAAAGG	10966
rs559400983	snp	A/C	0.00438332	0.0466095	intron-variant	RAB40B	GRCh38.p7	17:82676730	CCTCCTGGATTCAAG[A/C]GATTCTCCTGCCTCA	10966
rs559533587	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82691676	GACAGAGCGAGACTC[C/T]ATCTCAAAAAACAAC	10966
rs559538048	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82677655	TCCTCGTCCACCACC[C/T]GTCTCCAGGGCCAGC	10966
rs559549139	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82676302	CCTCACCTTCAACAG[C/T]CTCTCCCTCCACACA	10966
rs559593778	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82688352	GGGCACGGTAGCTCA[C/T]GCCTGTAATCCCAGC	10966
rs559607775	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82673135	CTTGAACCCGGCAGG[C/T]GGAGGTTGCAGTGAG	10966
rs559620690	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82692693	AAGGTAAAACGATGC[C/T]TGTAGAGAACATTTT	10966
rs559639964	snp	A/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82682867	AAAACGAACCCGGCC[A/G]GGCACGGTGACTCAT	10966
rs559675604	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82673737	AACTGCACACCTTGT[A/G]GGCCTTGCTGTAGGG	10966
rs559809299	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82678203	TCTGTGTTACCTTAC[A/G]TTTTGGTCCACGAGA	10966
rs559816256	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82663858	GATTCCCAGCCACAG[C/T]GCTATGTCCGTTCTG	10966
rs559874308	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82675526	ACCTTAGCCAGTGGG[A/G]TTGCTATAATGAAAA	10966
rs559906587	snp	A/C	0.00199481	0.0315187	intron-variant	RAB40B	GRCh38.p7	17:82686312	AGATGGGATTTCCCC[A/C]TGTTGGCCAGGCTGG	10966
rs559915003	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82691824	CCTGGGCCAGCCTGG[C/T]GACGCCTTCCTTCTA	10966
rs559969740	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82693773	TCACATAACGGGGGC[C/T]AGAGACACAGTCACA	10966
rs559983120	snp	A/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82658319	CCCAGGAGCTCCCTC[A/G]TGAGCTTTCTGACAA	10966
rs559987919	snp	A/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82690680	TGTGCACGTGTGTGC[A/T]GGGGAAGATCTGCAG	10966
rs560013766	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82684040	AGCCTGGCCAACATG[A/G]TGAAACCCTGTCTCT	10966
rs560041107	snp	G/T	0.000399281	0.0141238			GRCh38.p7	17:82655655	GAGGTCGGCCCTGTC[G/T]TTCTCACCCCACCTG	10966
rs560050458	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82691042	GGAGCCTTCTCCCAA[C/T]ATTAAACATTGGAAA	10966
rs560135056	snp	C/T			intron-variant, downstream-variant-500B, utr-variant-5-prime	RAB40B, MIR4525	GRCh38.p7	17:82668166	TCAGCTCTCAGCAGA[C/T]AGGGTAGCTCTCCGC	10966
rs560177482	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82659979	CTGGATGGATTGCAC[A/G]CATACACGTGCACAT	10966
rs560210360	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82675101	ACATCTGACACCCCC[C/T]AAACTGGGAAAAGCT	10966
rs560284781	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82686474	TAGGTGGGCCCTAAA[C/T]CCAATGGCTAGTGTT	10966
rs560354941	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82674112	TTGGGAGGCCGAGGC[A/G]GGCGGATCACCTGAG	10966
rs560462863	snp	A/T	0.000399281	0.0141238			GRCh38.p7	17:82655193	CAAATATTTATTTTC[A/T]CGTAGCTCTGGAAGC	10966
rs560487841	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82687659	TCTCCAGGACATGGC[C/T]GCCAGCTTCTGTGAG	10966
rs560528869	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82687919	TCTACTAAAAATAAA[A/G]TAATTAGCCGGGCAT	10966
rs560549035	snp	C/T	0.00438332	0.0466095	intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660838	CAACCAACCACTCTA[C/T]AGCACGTTTTTAGAC	10966
rs560594692	snp	A/C	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82687076	CTCTTGTCTGTGGGC[A/C]CCCCCACACCCCCGA	10966
rs560657406	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669241	AGCACTTTGGGAGGC[C/T]GAGCGGGGTGGATCA	10966
rs560768328	snp	A/G	0.00199481	0.0315187	intron-variant	RAB40B	GRCh38.p7	17:82664728	AGGGGCCCTGCCTGC[A/G]CCCTCCCGCACCCGG	10966
rs560884778	snp	C/T	0.000798403	0.0199641	intron-variant, missense	RAB40B	GRCh38.p7	17:82662570	ACCCAGTTGTGGGCA[C/T]CAGGAAGGACCACAC	10966
rs560890076	snp	A/C	0.0023933	0.0345097	intron-variant	RAB40B	GRCh38.p7	17:82697406	CCTGGGGCTTCCCAG[A/C]CCCTTCCCAGGCCCC	10966
rs560936306	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82694424	GTAATCCCAGCTACC[C/T]GGGAGGTTGAAGCAG	10966
rs560941526	in-del	-/CG	0.00159617	0.0282053	intron-variant, downstream-variant-500B	RAB40B, MIR4525	GRCh38.p7	17:82667795	AGACGCCACCTGCCC[-/CG]CGTGATGAGGCTCAG	10966
rs560978331	in-del	-/A	0.00279162	0.0372561	intron-variant	RAB40B	GRCh38.p7	17:82679280	ATTATTATTATTATT[-/A]TTATTTTATTTTATT	10966
rs560999668	snp	A/C	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82689606	CAATGGTGTTATTTT[A/C]AAATGCATAGAGACA	10966
rs561000216	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82659509	AGCCCTGGAGGGCCC[A/G]GCCCTAATTCCTGGC	10966
rs561048057	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82658882	GACGTAAATAGTTAC[A/G]GTGCGGCCGCACTGA	10966
rs561050568	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668810	GGCACGCAGGGAAGG[C/T]GGAGCTGCTGCCTGA	10966
rs561110325	snp	C/T			downstream-variant-500B	RAB40B	GRCh38.p7	17:82656968	GTGGTGAGCCCAGAT[C/T]GTGCCATTGTACTCC	10966
rs561127001	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82674293	GCAGTGAGCCAAGAT[C/T]GCGCCATTGCACTCC	10966
rs561143842	snp	A/C	0.0023933	0.0345097	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82700606	GGCTATTACCTAGTG[A/C]GGAAAGGGTACCTTC	10966
rs561170729	snp	G/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82667237	CCCAGGAGGCAGTGT[G/T]CCGAGTTCCTGGTCT	10966
rs561184550	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82663271	GGACAGGTAAGAGAA[A/G]GGGGTCCCAGCTGCT	10966
rs561300660	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82664268	GCTGGGCCGATGGTG[A/G]TGGGGGGAGGGTGCT	10966
rs561361288	snp	A/G	3.29919e-05	0.00406138	synonymous-codon	RAB40B	GRCh38.p7	17:82659613	CCATCGATCAATGCC[A/G]TCAAAAGACCAGCGG	10966
rs561363999	snp	C/G	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82674572	TGAACCCAGGAGGCG[C/G]AGCTTGCAGTGAGCC	10966
rs561372845	in-del	-/G	0.00835141	0.0640778	intron-variant	RAB40B	GRCh38.p7	17:82673357	AATTTCACTTTCTTT[-/G]GGGGCATCTTTCCAG	10966
rs561540574	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82676206	CAAAGGCTCCAACTC[C/T]TCCCCAAACCTCTGT	10966
rs561576126	snp	C/T	0.0023933	0.0345097	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661541	TGAGTTCTCAGATGA[C/T]GGCACACGCAGCAGG	10966
rs561581992	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82685517	AGCAGTGAAACGCTC[A/G]GATGGGGCGGGCCCC	10966
rs561641796	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82679105	AGCCAGGATAGTCTC[A/G]ATCTCCTGACCTCGT	10966
rs561789790	in-del	-/GGCTCAGGAGCAC	0.00438332	0.0466095			GRCh38.p7	17:82656496	GGAGCTCCTCACCGA[-/GGCTCAGGAGCAC]GGCTCTGATTTCTCA	10966
rs561796625	snp	C/G	0.00676609	0.0577691	intron-variant	RAB40B	GRCh38.p7	17:82693277	CTCTGAAAGTGCTGG[C/G]ATTGCAGACGTGAGC	10966
rs561803647	snp	A/G	0.0023933	0.0345097	intron-variant	RAB40B	GRCh38.p7	17:82687014	ATCAAAGACCCTCCT[A/G]TCCAGTGCTGGGGGG	10966
rs561843066	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665393	GAGTAGCCGGGACTA[C/T]GGGCATGTGCCACTA	10966
rs561866555	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82682116	CTATACACACACACA[C/T]GCATGCACACACACA	10966
rs561943679	snp	G/T			intron-variant	RAB40B	GRCh38.p7	17:82684188	ATTGCGCTTTTGCAC[G/T]CTAGCCTGGGTGAGA	10966
rs561976128	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82688062	GGGCAATAAGCCAGA[C/T]CCGGTTTCAAAAAAG	10966
rs561983462	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82664790	GTGGGGGTCAGGCTC[A/G]CATCACCCTGGCCCA	10966
rs562016421	snp	A/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82692714	AGAACATTTTTTTTT[A/T]AAATCTGGGAGCAGC	10966
rs562041475	snp	A/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82672651	GACACCTGAGCTGAC[A/G]GGCTTGCGCGATGCC	10966
rs562059969	snp	A/C	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82677112	CGCCACCACGCCCAG[A/C]TAATTTTTGTATTTT	10966
rs562073907	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82687832	ATCTCAACACTTTGG[A/G]AAGCTGAGGCAGGAG	10966
rs562075936	snp	A/G	0.00199481	0.0315187	intron-variant	RAB40B	GRCh38.p7	17:82693227	AGCCAGGCTGGTCTC[A/G]AACTCTTGACCTCTG	10966
rs562229298	snp	A/C	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82684262	AGATACCACTGCACA[A/C]CCATGAGTGGCTAAC	10966
rs562238815	snp	C/T	4.94344e-05	0.00497139	synonymous-codon	RAB40B	GRCh38.p7	17:82658067	AATGGGGAGCGGGAG[C/T]TTGTCCACCAGGTGC	10966
rs562257491	snp	C/T	0.00597247	0.0543191	intron-variant	RAB40B	GRCh38.p7	17:82674300	GCCAAGATCGCGCCA[C/T]TGCACTCCAGCCTGG	10966
rs562320383	snp	A/C			intron-variant	RAB40B	GRCh38.p7	17:82675470	ATGGCACTCCCTTTA[A/C]CCCATACTTCAGAAC	10966
rs562347386	snp	A/G	0.00478085	0.0486577	intron-variant	RAB40B	GRCh38.p7	17:82690642	GCATGGAGTGTGCAC[A/G]TGTGTTCCCGGGGAG	10966
rs562378768	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699267	CGCGGTCTCTCCCCA[A/C]GGTTCATCCAGGGCC	10966
rs562421598	snp	A/T	0.00279162	0.0372561	intron-variant	RAB40B	GRCh38.p7	17:82695097	TAAACCTGGACAATA[A/T]AAAAATAACAGCCTG	10966
rs562477874	snp	A/C	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82686266	ACAGGCACCTGCCAC[A/C]ACGCCCAGCTAATTT	10966
rs562516109	snp	C/G	0.00119737	0.0244387			GRCh38.p7	17:82656406	AGCGGCCCTGGAGGT[C/G]TTTGCGGTCAGCCCT	10966
rs562574118	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82685960	AGGTGCCCGCCACCA[C/T]ACCCAGCTAATTTTT	10966
rs562576472	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	RAB40B	GRCh38.p7	17:82656928	CTGAGGCAGGAGAAT[C/T]GCTTGAACCCGGGAG	10966
rs562602429	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82679877	GTGGCAGCTGCTGCC[C/T]GAGCAGGCTGCGGGG	10966
rs562792300	snp	A/G/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82660055	GCACACACAGTGCAC[A/G/T]TACCTGCACACATGT	10966
rs562847572	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82689811	GTCTCCACTAAAACT[A/G]CAAAAAATTAGCTGG	10966
rs562978253	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82658807	TCGAGGAACCCCCCA[C/T]GAGTTCATGTCCACC	10966
rs562989197	snp	A/C	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82664703	CCTCCCTGTGTCTGC[A/C]CAAGCTCACAGGGGC	10966
rs563002427	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82691660	GCACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC	10966
rs563132358	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82675065	CCCACAAAGCACAAT[A/G]ACTGGAGAGAGAGAG	10966
rs563187009	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82662086	GAGACACAACCTCAC[A/G]GATGAGCGGTGGGAC	10966
rs563251229	snp	A/T			intron-variant	RAB40B	GRCh38.p7	17:82681628	ACTTACTATACAATA[A/T]ATTAAAAGTAAAAAT	10966
rs563320433	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666670	GATGAGCACCAGGTC[C/T]GTCATTGAGAACATG	10966
rs563399779	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82673775	TGGCCAGGCTGACCA[C/T]TCCATGGGCCTTTCA	10966
rs563402219	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82679039	AGGCACCTGCCACCA[C/T]GCCTGGCTAATTTTT	10966
rs563414347	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82693825	CAGTGGCTCACGCCT[C/G]TAATTCCAGCACTTT	10966
rs563460078	snp	A/C	0.437683	0.165152	intron-variant	RAB40B	GRCh38.p7	17:82672320	TGTACTGACACACCC[A/C]ACCCCTGTAACTCTA	10966
rs563465489	snp	C/G	0.00159617	0.0282053	intron-variant	RAB40B	GRCh38.p7	17:82674230	CTGTAATCCCAGCCA[C/G]TCAGGAGGCTGAGGC	10966
rs563470728	snp	C/T	0.00517822	0.0506191	intron-variant	RAB40B	GRCh38.p7	17:82689186	TCTTCACTCCAAATG[C/T]ACCCAGCGCGGAGCA	10966
rs563535963	snp	C/T	0.0023933	0.0345097	intron-variant	RAB40B	GRCh38.p7	17:82678240	GAAACATTTTTGACA[C/T]CAGCAGTGTTAGCGT	10966
rs563536176	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666983	TAAAGGGAAGCGCGC[C/T]GCTGAGAGGCCGAGG	10966
rs563547072	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82667151	AGGCTGCGGAGGCCA[C/T]GGTTCTCAAGCAGCT	10966
rs563687716	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668307	ACATCCCCCCTCTGA[C/T]AAAAGCACCGAGTCC	10966
rs563732629	in-del	-/ACAC	0.27943	0.248262	intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660692	CACACACATGTACAC[-/ACAC]ACACACACACAGGCA	10966
rs563745111	snp	C/T	0.00199481	0.0315187	intron-variant	RAB40B	GRCh38.p7	17:82663900	TCTGGATGACGGGGG[C/T]CCAGACAACCGGACC	10966
rs563798861	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82675649	GTCTGACGAGGGCTG[C/T]ATCCTGGTTCATGGA	10966
rs563799249	snp	A/C	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82682076	GCATGCAGATTAAAA[A/C]CATCTCGATTACCAG	10966
rs563800381	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82684555	CCTCAGAGGGTGGGT[A/G]GGTGATGGACTGTGG	10966
rs563862146	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82676119	AATGGGGAACCGACC[A/G]CCTCGTGGGACGCAC	10966
rs564012509	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82686363	GTGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGA	10966
rs564122322	snp	C/T	0.00159617	0.0282053	intron-variant	RAB40B	GRCh38.p7	17:82688378	CCAGCACTTTGGGAG[C/T]CCGAGGCGGGTAGAT	10966
rs564259576	snp	C/T	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82686644	GTCAGGAAGGGTCCC[C/T]GCTTAGAGCCTGCCA	10966
rs564360924	snp	A/T			intron-variant	RAB40B	GRCh38.p7	17:82690071	GTTCAAACTTGAAAG[A/T]GATGACTTTATAAAT	10966
rs564418860	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82697797	GAGCTCTGGGCGCTC[C/T]GGCCTCCCCTCGCCC	10966
rs564470692	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82676905	TGCTGGGATTATAGG[C/T]GTGAGCTACCGCGCC	10966
rs564479327	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698660	CAGAGGCGGCGGCCC[A/G]GCCCCGAGAGGCGCC	10966
rs564564637	snp	C/T			upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699667	GCTTCTATGCATGCG[C/T]TCCTATGTGTGCGTG	10966
rs564605842	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82682873	AACCCGGCCGGGCAC[A/G]GTGACTCATGCCTGC	10966
rs564619923	in-del	-/T	0.00676609	0.0577691	intron-variant	RAB40B	GRCh38.p7	17:82686287	CAGCTAATTTTTGTA[-/T]TTTTAGTAGAGATGG	10966
rs564658135	in-del	-/AA	0.0111632	0.0738715	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657667	ACACACATCGAAAAC[-/AA]GAGCTTCATGCACAT	10966
rs564777295	snp	C/T	0.00398564	0.0444627	intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660872	CAGCACCAATTTATA[C/T]GTAAGCTTAACCGCC	10966
rs564782100	in-del	-/CACT	0.00358779	0.0422022	intron-variant	RAB40B	GRCh38.p7	17:82660439	AAACACACGCACAGG[-/CACT]CATGCAGATGCACGC	10966
rs564840414	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82692265	AGGCAGAGCAGTGGG[C/G]TCCACATAGTCTGTG	10966
rs564862723	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82685949	GCTGGGATTACAGGT[A/G]CCCGCCACCACACCC	10966
rs564873116	snp	A/G	0.0023933	0.0345097	intron-variant	RAB40B	GRCh38.p7	17:82679135	TGATCCACCTGCCTC[A/G]GCCTCCCAAAGTGCT	10966
rs564900028	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82658906	GCACTGAATTAGGGC[C/G]CTCATCTAATGACTG	10966
rs564900990	snp	A/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82660010	ACACATGGAGCTCAC[A/G]CACACACAGGCACTT	10966
rs564956843	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82690206	CATGTGTGTCCAGGG[C/G]AAGATCTGCAGAATT	10966
rs564968792	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82660364	GTGTACACACACACA[C/T]GCACAGGCACTCATG	10966
rs565010560	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82685538	GGCGGGCCCCAGGCA[C/T]CCGGCCTGCCTCCAG	10966
rs565072249	in-del	-/AT	0.303187	0.244277	intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660684	CGTACCTGCACACAC[-/AT]GTACACACACACACA	10966
rs565118551	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82659227	GTCACCATTGCCAGG[C/T]GGGCTGGTCTGCGTG	10966
rs565179319	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B, utr-variant-5-prime	RAB40B, MIR4525	GRCh38.p7	17:82668198	GCTGGTCATCCCGAC[A/G]TCCGCGTTGCTCTGA	10966
rs565180523	snp	A/T	0.00318978	0.0398085	intron-variant	RAB40B	GRCh38.p7	17:82664300	CCCGGGGTGCTGTGC[A/T]GATGGTGGTGGGGCT	10966
rs565183479	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82663444	ATCCCCACCGCCCCA[A/G]AGCTGGAACCGCAGG	10966
rs565283011	snp	A/G	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82691103	CCCCGGTGTGTCCAC[A/G]CACCGTGTAGTCTTG	10966
rs565314469	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82674966	AGCCCCTCAACCTGC[C/T]GGCTGTGTGGGGCAC	10966
rs565378061	snp	A/G	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669430	TGGTGAGCCGAGATC[A/G]CACCATTTCACTCCA	10966
rs565454269	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668853	GAGGCCCAGCCATGC[C/T]TCCGCTGCAGCCGGC	10966
rs565487642	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82687196	TTCTCTCCTCAAACA[C/T]ACGTGGCCTCCTGAG	10966
rs565518496	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665523	CCTCCCAAAGTGCTG[A/G]CATTACAGGCATAAG	10966
rs565530307	snp	G/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82679746	AGGTCACCGAGCACA[G/T]GGCAGGGGGCAGCCT	10966
rs565550416	in-del	-/TC			intron-variant	RAB40B	GRCh38.p7	17:82686726	CTGTGAGAGAATAAA[-/TC]TCTGTTTCAATTTGT	10966
rs565586206	snp	A/C	0.00755907	0.0610114	intron-variant	RAB40B	GRCh38.p7	17:82674604	AGATCGCGCCACTGC[A/C]CTCCAGCCTGGGCGA	10966
rs565636323	snp	A/C	3.31851e-05	0.00407326	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657815	CTGCCGGGGGTAACG[A/C]CGAGCTTCTCCTGGA	10966
rs565688680	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699640	CTTTGCATGTGTGTG[C/T]CTGCGTGTGCTGCTT	10966
rs565749182	snp	G/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82698049	CCCGCGGCCGAACGC[G/T]CACTTGCGGACTCGA	10966
rs565749450	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82700271	TCCCAAGTAGCTAGG[A/G]TTACAGGCATGTGCC	10966
rs565820996	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82697541	GAGGCGCGGCAGGAA[A/G]GTGGGCACAGGCTGG	10966
rs565921261	snp	A/G			downstream-variant-500B	RAB40B	GRCh38.p7	17:82656823	GTTCAACACCAGCCT[A/G]ACCAACATGGTGAAA	10966
rs565927273	snp	A/G	0.00199481	0.0315187	intron-variant	RAB40B	GRCh38.p7	17:82674113	TGGGAGGCCGAGGCG[A/G]GCGGATCACCTGAGG	10966
rs565978511	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82670578	CTTACTCTGTCGCCC[A/G]GGCTGGAGTGCAGTG	10966
rs565983058	snp	C/T	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82658233	CGCCCTCCCAAGGCT[C/T]GGACGCCCGTGGCCC	10966
rs566000702	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82685099	GCCTGGGTGACAAGA[A/G]TGAAACTCTGTCTCA	10966
rs566006222	snp	C/T	0.00159617	0.0282053	intron-variant	RAB40B	GRCh38.p7	17:82683048	CTCGGGAGGCTGAGG[C/T]AGGAGAATTGCTTGA	10966
rs566058488	snp	A/G	0.00199481	0.0315187	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82662157	CGGTGACCACCCTCA[A/G]CACGAGAGAGAAGGG	10966
rs566075285	snp	A/G	0.00755907	0.0610114	intron-variant	RAB40B	GRCh38.p7	17:82677911	GGCCCAGCGAGCAGC[A/G]ACCAAACTCATTTCA	10966
rs566117416	snp	G/T	0.00199481	0.0315187	intron-variant	RAB40B	GRCh38.p7	17:82672745	CCAGCCTCCAGAACT[G/T]TAAGAAATGCATTTA	10966
rs566119292	snp	G/T	9.91834e-05	0.00704144	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657860	TTTCTTTCAGTGCCT[G/T]CCTTAAGAAATTTTG	10966
rs566131466	in-del	-/GT			upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699359	CGTGTGCATGTGTTC[-/GT]GTGTGTGCATGTCTG	10966
rs566138092	snp	A/G	0.00914312	0.0669923	intron-variant	RAB40B	GRCh38.p7	17:82676906	GCTGGGATTATAGGC[A/G]TGAGCTACCGCGCCC	10966
rs566139483	snp	C/T	0.00874735	0.0655527	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671326	TCTAACACACTCACA[C/T]GCTCTCTGTACTGAC	10966
rs566193587	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666952	ACAAGTATGGCTGAA[C/T]AGGGAATCAGAATTC	10966
rs566202402	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82688488	GGCGTGGAGGCAGGC[A/G]CCTGTAATCCCAGCT	10966
rs566279928	snp	A/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82676988	GAGTCTCACTCTGTC[A/G]TCCAGGCTGGAGTGC	10966
rs566394357	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82685628	TCCAGTGCTGAAGCT[C/T]CAAGAAGAGGGGACC	10966
rs566456818	snp	G/T	0.0879971	0.190408	intron-variant	RAB40B	GRCh38.p7	17:82664361	GTGGTGGTGGGAGGG[G/T]GTTCCCGGGGGCGCT	10966
rs566504675	snp	A/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82659795	GATTTATCAACTGAA[A/T]GTAGCAGTTTTATGA	10966
rs566512228	snp	C/T	1.65143e-05	0.00287348	missense, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82664520	AGCTTCACCCGCCGC[C/T]CGTCCAGCAGGATGG	10966
rs566538116	snp	C/T	0.00478085	0.0486577	intron-variant	RAB40B	GRCh38.p7	17:82679926	GCTCACGAAGAGACA[C/T]CGTCTTGGGGAAGGG	10966
rs566546284	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82670969	CACCCGAACCCCTGT[C/T]TCCCTTCCCCATTTT	10966
rs566598765	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82670015	TTTTCGAATGCGGAG[A/G]TAACTCCAGCTTTGA	10966
rs566647646	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82674447	CCATCCTGGCTAACA[C/G]GGTGAAACCCCGTCT	10966
rs566915631	snp	C/T	0.000399281	0.0141238			GRCh38.p7	17:82655853	CCCCAAGCCTGGGTC[C/T]ACCCGCAGGGACCAG	10966
rs566934254	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82686849	TTCCTCCACGTTCCT[C/T]CCGTCCAGTGCTGGG	10966
rs567039276	snp	A/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82696867	ATCTAGAAATGTGAC[A/G]AATGGAAGCTTTTTG	10966
rs567157832	snp	A/G	0.00119737	0.0244387			GRCh38.p7	17:82655366	GGTGAACACCTCCAA[A/G]GAGCTCTGAGTCACA	10966
rs567171897	snp	C/T	0.0023933	0.0345097	intron-variant	RAB40B	GRCh38.p7	17:82698282	GCTCCTCCTCAGCCC[C/T]GCGCCCCCGGACCGG	10966
rs567215542	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82684028	GAGTTCGAGACCAGC[C/T]TGGCCAACATGGTGA	10966
rs567220669	snp	A/C	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82691393	CCTGTCACCAATAAA[A/C]ATGTGCAAAAGGCCG	10966
rs567245692	snp	C/T	0.00279162	0.0372561	intron-variant	RAB40B	GRCh38.p7	17:82677766	GTCTGCTGGAACCCC[C/T]GGATGTGGGGCCCTC	10966
rs567383336	snp	A/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82684651	TCAGAGGCTCAGGGC[A/T]GCTGAGTGACCGGAG	10966
rs567417969	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82658214	GTGCCCACACCTGTT[C/G]TCCCGCCCTCCCAAG	10966
rs567500411	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RAB40B, MIR4525	GRCh38.p7	17:82667786	CCCGCTTTGCAGACG[A/C]CACCTGCCCCGTGAT	10966
rs567517743	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82659336	CCACGCATAGCCGAG[A/G]TACGCCGTGGACGCT	10966
rs567544977	in-del	-/CTTTC	0.00318978	0.0398085	intron-variant	RAB40B	GRCh38.p7	17:82659747	ACAACTAAATAACCA[-/CTTTC]CTTATTTTAACACAA	10966
rs567551891	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82693020	TTTTTCTTTTTTTTT[A/G]GAGACAGAGTCCCAC	10966
rs567552967	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82662104	TGAGCGGTGGGACGC[A/G]GCATGGTTTTGCTGT	10966
rs567575035	snp	A/C	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82673429	CCTGGGGCCCCCACT[A/C]CCTTACTGCTGGATT	10966
rs567612695	snp	C/T	0.00358779	0.0422022	intron-variant	RAB40B	GRCh38.p7	17:82693477	GGTGGGAGCACCAAG[C/T]GAAAAATGCTTTGCG	10966
rs567637752	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82667412	CATGAGCACGTGCAT[A/G]GCACACCTGCCTGAT	10966
rs567701598	snp	C/T	0.0792508	0.182605	intron-variant	RAB40B	GRCh38.p7	17:82695210	TTCTTTTTTTTTTTT[C/T]GAGACAAAATCTCAC	10966
rs567718554	snp	A/T	0.0948562	0.196037	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82700414	GGGATTGCAGCACTG[A/T]TTTTTTTTAGAAGGA	10966
rs567749976	snp	G/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82659025	GGAGGGCCCAGGGTT[G/T]CTGGCACCGCCGAGA	10966
rs567798969	snp	A/C	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82697525	GCGTGGGTTCAGCCC[A/C]GAGGCGCGGCAGGAA	10966
rs567860694	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82691867	GAGAAATGGAACTTC[C/T]GAGGGGAAAGAGCGT	10966
rs567887574	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82663561	TGCCCCGGGCTTGCC[C/T]CAAGGTGAGGAGCTG	10966
rs567932752	snp	C/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82694472	GGGAGGTGGAGGTTG[C/G]AGTGAGGTGAGATCA	10966
rs567968358	snp	A/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82675306	ATTAGCACAGCCCGG[A/G]TGCATAACCCACACC	10966
rs568023116	snp	C/G	0	0	intron-variant, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82664874	GTTTGCCGCGGGGCT[C/G]TGGCCGCTGGGTGTG	10966
rs568048241	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	RAB40B	GRCh38.p7	17:82656693	TACACCAGGCAGTGG[C/T]GCAGTGAAGTAAAGG	10966
rs568167031	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82680509	AGTTAAAAAAAATAT[C/T]GCATATGAAAAAGCT	10966
rs568229499	snp	C/T	0.00358779	0.0422022	intron-variant	RAB40B	GRCh38.p7	17:82676696	GCAATGGCGTGATCT[C/T]AACTCACTGCAACCT	10966
rs568252146	snp	A/G	0.00199481	0.0315187	downstream-variant-500B	RAB40B	GRCh38.p7	17:82657002	CTGGGCAACAAGAGC[A/G]AAACTCTGTCTCAAA	10966
rs568292774	snp	C/G	0.00676609	0.0577691	intron-variant	RAB40B	GRCh38.p7	17:82659378	GACCAGCTTCCTGAG[C/G]TTTCGTGATTGTAGC	10966
rs568314649	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82686713	CTGGTCTCTAGAACT[A/G]TGAGAGAATAAATCT	10966
rs568377701	snp	C/T			intron-variant, downstream-variant-500B, utr-variant-5-prime	RAB40B, MIR4525	GRCh38.p7	17:82667941	TGGCATGGGCGCTGA[C/T]GGGGCACTGATGGGG	10966
rs568381211	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82687163	GACGCAATTTGAACC[C/T]GTGAGTGTACCACAG	10966
rs568386476	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699017	GTTTACACTCTCGCG[C/T]GCGCCCGTGAGCGCC	10966
rs568402645	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661754	TAGCTGGACATGGTG[A/G]TGTGCTCCTGTAGTC	10966
rs568441862	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666099	CTGCCACCGCACCTG[A/C]CACCACACCTGCCAC	10966
rs568614649	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82664171	GGGTGTTCCCCGGGG[A/G]CGCTGTGCCGACGGT	10966
rs568632876	snp	A/C/G	0.00159649	0.0282165	intron-variant	RAB40B	GRCh38.p7	17:82683000	ATACAAAAATTAGCC[A/C/G]GGCATGGTGGCACAC	10966
rs568688647	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82682490	TGACAAGTCTCCCCA[A/G]TTGATCTATAGTTTT	10966
rs568816768	in-del	-/A	0.113334	0.209338	intron-variant	RAB40B	GRCh38.p7	17:82673204	TGAGACTCTTGTCTC[-/A]AAAAAAAAAATTGCC	10966
rs568830501	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668659	GCTCCACGACTGGAG[A/C]GGGCGTGGGGAGTGA	10966
rs568942430	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82679208	AGTCAGGAGCAGCTC[A/G]CGCCCACCAGCAACC	10966
rs568944157	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82674076	CCAGGCGCGGTGGCT[C/T]GCGCCTGTAATCCCA	10966
rs568964570	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82685614	ACAGGGCCAGGGGCT[C/T]CAGTGCTGAAGCTCC	10966
rs569006178	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82674393	CCCCAGCACTTTGGG[A/G]GGCCAAGGTGGGCGG	10966
rs569019121	snp	C/T	0.000399281	0.0141238			GRCh38.p7	17:82655793	ACACCCCTGCCTCCC[C/T]GTGGACTTTGTCCCC	10966
rs569080359	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82678704	CAGACTGGCGGTCCC[C/T]GGGGCAGAGGGGAGG	10966
rs569103069	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82689692	AGTAGAAAACTGGCC[A/G]GGCACGTGGCTCACA	10966
rs569232383	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82659431	GTTGTGCCGAGGTGA[A/G]GCACCCTCCTTCCTG	10966
rs569241477	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82688903	CGCACCACTGCACTC[C/T]AGCCTGAGCAACAGA	10966
rs569302347	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82686158	CATCCAGGCTGGAGG[C/T]TGGAGTGCAGTGGCA	10966
rs569344842	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82691176	CTCAAGATGATTCCC[C/T]CTCTCAGTAAGTGAG	10966
rs569407955	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668893	GCAGCCACTCTAGAT[A/G]GGCCACTGCTACCAT	10966
rs569421947	snp	A/G	1.70429e-05	0.0029191	intron-variant	RAB40B	GRCh38.p7	17:82658149	ACTTGGGAGAGAAAA[A/G]ATAAACCTTGCTTAG	10966
rs569456639	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82683091	GAGCTTGCAGTGAGC[C/T]GAGATCATGCCACTG	10966
rs569472850	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82664341	CCCGGGGTGCTGTGC[C/T]GACGGTGGTGGTGGG	10966
rs569498087	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661661	GGAGACCGAGGCAGG[C/T]GGATCACCCGAGGTC	10966
rs569631891	snp	C/G	0.00517822	0.0506191	intron-variant	RAB40B	GRCh38.p7	17:82687946	GCATGGTGGCATGCA[C/G]CTATAGTCCCAGCCA	10966
rs569722114	snp	G/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82694592	AAACTCAAAGAGTAC[G/T]TTCATACTAAAAGTT	10966
rs569775444	snp	G/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82688432	AGCCTGACCAACATG[G/T]TGAAACCCCATCTCT	10966
rs569787484	snp	A/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82678336	AATATAATAAAGATA[A/T]ACAAAGCTTCTAGAA	10966
rs569821234	snp	A/G	0.0178098	0.0926698	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82698960	CTGCTCCCGCAGCCA[A/G]TGGCGGGGCGGGGTG	10966
rs569860812	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82693997	CTGAGACAGGAAAAT[C/T]GCTTGAACCTGGGAG	10966
rs569883058	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82692931	AACACTCCTAGCAAG[C/G]ATTGAAAGAAATTCA	10966
rs569894318	snp	C/T	0.0429648	0.14013	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671170	ACAGTCACACACATC[C/T]TGTACTCACTGACAC	10966
rs569909877	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82673323	TCTAAATCTGCTCTC[A/G]GTACCTGCAAACATT	10966
rs569953006	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666007	GACTGCAGCCTCTAC[C/T]TCCTGGGCTCATAGG	10966
rs569957583	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82689286	TGCCTGCTCCAGCTG[C/T]GTCCACTCTGCACCA	10966
rs569980610	snp	A/G					GRCh38.p7	17:82656436	TGCTCTGAGGCAGTC[A/G]GGGTCAGGGGCTACA	10966
rs569984449	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82677261	CAGCCTACTAATTTA[A/G]ACAATTAATGTTCAA	10966
rs569988975	snp	A/C	0.00119737	0.0244387			GRCh38.p7	17:82656080	CAGCCTCCTGAGTAG[A/C]TGGGATTACAGGTGT	10966
rs570045212	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82672794	CAGTTTGTGGTATTC[C/T]GTTACAGCAACAGAA	10966
rs570069679	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82696970	GAGACCTGCCACCGA[A/G]CGGGGAGGGGGGTAG	10966
rs570079472	snp	A/T			intron-variant	RAB40B	GRCh38.p7	17:82694843	AGCCAAGATATCTCT[A/T]CATTGTTCAAAGATA	10966
rs570114267	snp	C/T	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82658964	ACACTCGGAGGAGGC[C/T]ATGTTACGCGAAGGC	10966
rs570145523	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666994	GCGCCGCTGAGAGGC[C/T]GAGGGGAGAAGCAGC	10966
rs570316741	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82677624	GGAACCCTGCCTTCC[C/T]GTGTCCACCTTCCAA	10966
rs570414701	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669754	GCCCTGTGAAATTAC[A/G]CTTTGAGCGACGACC	10966
rs570416027	in-del	-/G	0.00159617	0.0282053	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699874	CAGGCAGCAGGCAAA[-/G]GGCGAGCTCCGTCCA	10966
rs570444469	snp	A/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82660261	TGCACATGCATGCAC[A/T]TAAACAGGCAAGCAC	10966
rs570447847	snp	C/T	0.00478085	0.0486577	intron-variant	RAB40B	GRCh38.p7	17:82680597	ACCCATGGACAACTA[C/T]GATTAATATTTCAGT	10966
rs570554409	snp	A/G	0.00318978	0.0398085	intron-variant	RAB40B	GRCh38.p7	17:82675159	CAAGCAAAGTACAAT[A/G]ACCTCCACATCCCGG	10966
rs570752167	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82670637	CCTCCCGGGTTCAAG[A/G]GATTCTCCTGTCTCA	10966
rs570818034	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82682711	CTAGAAATAGGCCCA[C/T]ACAAAAATGGCCAAT	10966
rs570864695	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82664474	TGGGGGTGCGGGACG[C/G]TCGCACCTCCTCCAG	10966
rs570928634	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82682408	ACTAATAAAAGGAAT[C/T]AAAGAAGACCTAAAT	10966
rs570939539	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82697464	CTCCATCTCCACGCC[C/T]GGCTGCCCTCCTCCG	10966
rs570990011	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82676440	TTCAACAGCCTCTCC[C/T]CCCCCACACAGGGCA	10966
rs571036000	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82691774	CACCAGCTGGGGTGG[C/T]GGAAAGGCAGGGCCC	10966
rs571063939	snp	A/G	0.000399281	0.0141238			GRCh38.p7	17:82656554	GGGTGCCAGCTTTTA[A/G]CTCTCCGCTCTCTCC	10966
rs571071353	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82679681	GTGCTGCAGAGGCCA[C/T]GCCAACCCTGTGCGG	10966
rs571102935	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82686855	CACGTTCCTCCCGTC[C/T]AGTGCTGGGGGGAAG	10966
rs571150670	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82674406	GGAGGCCAAGGTGGG[C/T]GGATCATGAGGTCAG	10966
rs571219609	snp	C/T	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82674066	AACAACCTGGCCAGG[C/T]GCGGTGGCTCGCGCC	10966
rs571315562	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82679463	ATTTTTTGTATTTTT[A/G]GTAGAGACAGGGTTT	10966
rs571339718	snp	C/T	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82685108	ACAAGAGTGAAACTC[C/T]GTCTCAAAAAAGGAA	10966
rs571402806	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82678662	AATCTGTCTTATGTT[C/G]AGTTAAAACACCGGA	10966
rs571427982	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82688656	AGTTTTGTTTGGGCC[A/G]GGCGTGGTGGCTCAC	10966
rs571453014	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82685699	GAAACTGTCCTTTCG[C/G]GTTTCACCATCTATC	10966
rs571492083	snp	C/T	0.00398564	0.0444627	intron-variant	RAB40B	GRCh38.p7	17:82664086	GGGGAGGGTGCTCCC[C/T]GGGGTGCTGTGCCGA	10966
rs571517915	snp	C/G	0.000399281	0.0141238			GRCh38.p7	17:82655211	TAGCTCTGGAAGCCG[C/G]AAGTCCAAAACCAAT	10966
rs571553955	snp	C/G	0.00159617	0.0282053	intron-variant	RAB40B	GRCh38.p7	17:82659349	AGGTACGCCGTGGAC[C/G]CTCGTTTCGTCTGGA	10966
rs571557388	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82689213	AGCAGCCTGCACTCC[C/T]GGGGCAGGAGGAGCA	10966
rs571628462	snp	C/G	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82663646	CTCACCTCCCCACGT[C/G]TGGGTCCTCCACCCG	10966
rs571690786	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82690786	GCAGAATTGGAGGGA[C/G]ATGAAGTGTGCATGT	10966
rs571693330	snp	C/T	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82690351	AGCAGAGAGTGTGTA[C/T]GTGTGTCCAGGGGGA	10966
rs571721958	snp	A/G	0.000798403	0.0199641			GRCh38.p7	17:82654734	GTTTGTATTTTTAGT[A/G]GAGACGGGGTTTCAT	10966
rs571794524	snp	C/T	0.00398564	0.0444627	intron-variant	RAB40B	GRCh38.p7	17:82686983	CTGGGGGGAAGGAGG[C/T]TCAGAGCTCAGGGGT	10966
rs571870362	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B, missense	RAB40B, MIR4525	GRCh38.p7	17:82667928	GTCTCTCTCTTCTTG[A/G]CATGGGCGCTGACGG	10966
rs571878707	snp	G/T			intron-variant	RAB40B	GRCh38.p7	17:82675824	CAGCACCCGAATTTG[G/T]GGGGGTCACAAACAT	10966
rs571878830	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82692372	AGGAGGGAGAATCCA[C/G]GCCTCGCTGACCGTA	10966
rs571927964	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82685983	TAATTTTTGTATTTT[C/T]AGTAGAGACGGGGTT	10966
rs571941949	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82672986	AGGCAGGTGGATCAT[C/T]TGAGGTCAGGAGTTT	10966
rs571956385	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82676089	CTCCCCCGGGTCTCC[A/G]TTTCCCTGGCTATGA	10966
rs572045854	snp	A/G	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82662791	CTGTTCGGCCCACTG[A/G]GCAGCTGGGGTCAGG	10966
rs572128008	snp	C/T	0.000399281	0.0141238			GRCh38.p7	17:82656131	TTTTTGTAATTTTAT[C/T]AGAGACGGGGTTTCA	10966
rs572157386	snp	A/G			upstream-variant-2KB	RAB40B	GRCh38.p7	17:82700232	TCTTGGCTCACTGCA[A/G]CTTCCACCTCCTGGA	10966
rs572217462	snp	A/C	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82680845	GACCAGCCTGGATAA[A/C]ATGGTGAAACCCCGT	10966
rs572267004	snp	A/G	0.00199481	0.0315187	intron-variant	RAB40B	GRCh38.p7	17:82660349	CGTACCTGCACGCAC[A/G]TGTACACACACACAC	10966
rs572358392	snp	A/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82675173	TGACCTCCACATCCC[A/G]GAATTTCACTAACAA	10966
rs572430134	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82687690	AGGTGCTGGCATCCT[C/T]GGAGAGACTGAGAAG	10966
rs572438585	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82692583	CAACGGTGGCCGTGC[A/G]ATGCGGGGTGGGGGT	10966
rs572493895	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699194	TTGGCGGACGCGGCC[G/T]GAAGGCCCCCGCAGG	10966
rs572530867	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661448	ACTGTAAGAGCTCAC[A/G]TGGAGTCAGCCCTTC	10966
rs572545853	snp	A/G					GRCh38.p7	17:82656206	CTGCCTCGGCCTCCT[A/G]AAGTGCTGGGATTAC	10966
rs572592466	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661830	AGGCGGAGGTTGCAG[C/T]GAGCTGATATCGTGC	10966
rs572624408	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82670430	CCTCAGGTAATCCAC[C/T]TGCCTTGGCCTCCCA	10966
rs572672440	snp	A/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82676527	CGGCTCTTCCCAGCC[A/T]CCCCTACAAAGCACC	10966
rs572728226	in-del	-/CTCA	0.0023933	0.0345097			GRCh38.p7	17:82654578	TATTTGAGATGGAGC[-/CTCA]CTCTGTCACTCAGGC	10966
rs572730950	snp	C/T	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82659453	TCCTTCCTGCTGGAG[C/T]GCCATCCGGTGCCCT	10966
rs572788719	snp	A/C	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82690068	TCAGTTCAAACTTGA[A/C]AGTGATGACTTTATA	10966
rs572790320	snp	A/G	0.000399281	0.0141238			GRCh38.p7	17:82654965	ACAAGAAAATGACAA[A/G]GTTTCTCTAAGGTTT	10966
rs572809485	snp	C/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665313	GCTGGAGTGCAGTGG[C/T]GTGATCACAGCTCAC	10966
rs572825529	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668787	GCTGCCCCAGGGCAG[C/T]GGGCCGCGGCACGCA	10966
rs572882250	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82695051	CTAAATCATTGCGGG[C/T]ACTACAGCCACAATA	10966
rs572893566	snp	A/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82664404	GTGGGGGATGGGTGC[A/T]CCCCGGGGCACTGTG	10966
rs572913212	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82659172	CGGTTCTAGCAGCCC[C/T]GGGACACTCATACAG	10966
rs572916474	in-del	-/C	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82690230	CAGAATTGGAGGGAG[-/C]ACGGAGTGTGCACAC	10966
rs573016521	snp	A/G	0.00159617	0.0282053	intron-variant	RAB40B	GRCh38.p7	17:82678824	CACCTGCACCGTAAA[A/G]TGCTCACATCTGACT	10966
rs573027911	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669343	AGCCGGGCGTGGTGG[C/T]GGGTGCCTGTAATCC	10966
rs573064016	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B, utr-variant-5-prime	RAB40B, MIR4525	GRCh38.p7	17:82668174	CAGCAGACAGGGTAG[C/T]TCTCCGCAGCTGGTC	10966
rs573140591	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82673652	CTTTTGAGATCGGCC[A/G]TAAACTCATTCTTGA	10966
rs573201940	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82667709	CCAGAGCAAACTCCC[C/G]CCGTCAGAGGAGAGT	10966
rs573227098	snp	C/T	0.00159617	0.0282053	intron-variant	RAB40B	GRCh38.p7	17:82685906	CCTCCTGGATTCAAA[C/T]GATTCTCCTACCTCA	10966
rs573229575	snp	C/T	0.00279162	0.0372561	intron-variant	RAB40B	GRCh38.p7	17:82674932	GGCACCAGAATCCAG[C/T]CACGCCTGAAACTAC	10966
rs573290774	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82672877	GTTTATTTTTCCTTC[A/G]TGTACGAATTTTTGT	10966
rs573369336	snp	C/T	0.00199481	0.0315187	intron-variant	RAB40B	GRCh38.p7	17:82680142	AGGCCTGGCAGGGTT[C/T]GAGGGCTCAACTCAG	10966
rs573395605	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82674579	AGGAGGCGGAGCTTG[C/T]AGTGAGCCGAGATCG	10966
rs573429115	snp	A/G	0.0256215	0.110247	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671804	CCCCGTAACTCTAAC[A/G]CACACACTCACACCC	10966
rs573530335	snp	A/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82679714	ACTGCTGCCCCGCCC[A/T]GTCACTAAGCACCTG	10966
rs573629601	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82686195	CAGCTCACTGAAACC[C/T]CCGCTTCCGGGGTTC	10966
rs573643593	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82677042	CAAGCTCCACCTCCC[A/G]GGTTCAAGCAATTCT	10966
rs573783354	snp	A/G	0.00159617	0.0282053	intron-variant	RAB40B	GRCh38.p7	17:82689303	TCCACTCTGCACCAC[A/G]GTGGTGCCTGGTGCC	10966
rs573846936	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82693697	GGTAGAGTCACAAAA[A/G]GGATGTCACCACCAT	10966
rs573947258	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82667019	AGCAGCGCCGAGGCT[C/T]GCACCAGACCTCACC	10966
rs574144411	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82689655	TTAATTTTCTCACAA[A/G]TGGTACCGCAGGAGG	10966
rs574157495	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82658296	GTCCCCTCTGCCCAC[A/G]TACAGATCCCAGGAG	10966
rs574191509	snp	A/G	3.62161e-05	0.0042552	intron-variant	RAB40B	GRCh38.p7	17:82658719	CGGGGGCATGCTAGC[A/G]GGCAGGAGAAAGGCG	10966
rs574207848	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661967	AGTTCCCAGAGGAGG[C/T]GGCCCTGGGACAGCC	10966
rs574253114	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82696473	TCGTCTGGGCGTACA[C/T]GTTGTTGGGTGCTTT	10966
rs574294235	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82662399	CCAGCACGTGCTGTC[A/G]GAGTGCCCCATCGTG	10966
rs574315694	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82697002	ACATGCGGGGGCAGC[A/G]GCGCCTGGGGACAGG	10966
rs574315783	snp	A/G	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82691000	GAGGCTCTGATGCTC[A/G]TCTCCGGGAAGAAAA	10966
rs574346841	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669214	GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	10966
rs574351874	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82680977	AGTGAGCTGAGATTG[C/T]GCCATTGCACTCCAG	10966
rs574452134	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82686268	AGGCACCTGCCACCA[C/T]GCCCAGCTAATTTTT	10966
rs574524773	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82659943	GTAATCGCCACCTCT[C/T]GAGGAGTGTGGCCCA	10966
rs574552281	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82681373	CAGTTAGAAGCAGCC[A/G]TCTGGGAGAAGTCTC	10966
rs574597758	snp	A/G	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82688672	GGCGTGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	10966
rs574613967	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82682970	TAACAAGGTAAAACC[C/G]TGTCTCTATTAAAAA	10966
rs574614321	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82660327	GCACAGACTCATACA[C/T]AGGGCACGTACCTGC	10966
rs574626545	snp	A/C	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82664220	CCTGGGGTGCTGGGC[A/C]GATGGTGGTGGGGGG	10966
rs574738815	snp	C/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82698431	CCGCGCCCGCACCCC[C/G]GCACGCCCTCCGCCC	10966
rs574751364	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661317	TCTCAGATATTTAAA[G/T]ACATTCAATGTAGGC	10966
rs574789789	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665239	AACAAAAAAAAAACC[C/T]GAGAATGCCTTTCTT	10966
rs574827987	in-del	-/AG			intron-variant	RAB40B	GRCh38.p7	17:82660106	CTCATGCACAGACAC[-/AG]TGCACATACCTGCAC	10966
rs574848640	snp	C/T	0.00199481	0.0315187	intron-variant	RAB40B	GRCh38.p7	17:82692025	CGCACGGTCCGTGGG[C/T]TGAGGTGACAGGCAG	10966
rs574849549	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660798	ATGCACGCTTACATC[C/T]GTAATACTGATGAAG	10966
rs574889486	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665635	ACTTTGGGAGGCTGA[A/G]GCGGGTGGATCACTT	10966
rs574910271	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82692532	AGGCGGGCCAACGGT[A/G]CAGACCCAGACCCAC	10966
rs575080647	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82670333	GGAATTACAGGCACA[C/T]GCCAGCAAGCCAAGC	10966
rs575113450	in-del	-/AC	0.0590317	0.161342	intron-variant	RAB40B	GRCh38.p7	17:82660355	TGCACGCACGTGTAC[-/AC]ACACACACGCACAGG	10966
rs575129702	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82663694	CCGCTGGCACCAGGA[C/T]GCTCCGAGCTCCCTG	10966
rs575149872	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82675472	GGCACTCCCTTTACC[C/G]CATACTTCAGAACTG	10966
rs575241712	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82676018	TGGTAAAGCACAGAC[A/G]CTGCAGCCTGGGGCC	10966
rs575253148	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82667615	GGCTTCCCGCATCCT[C/T]CTCTGTCTCCTGCTA	10966
rs575272278	snp	A/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82694397	ATTGGCCCAGTGTGG[A/T]GGCAGGCACCTGTAA	10966
rs575312936	snp	C/T	0.00199481	0.0315187	intron-variant	RAB40B	GRCh38.p7	17:82663233	AGGACTGGCCACTAC[C/T]AGACGGGGCAGGCGT	10966
rs575333627	snp	C/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82695023	CTGACTGTATTTAAA[C/T]GTTGAATTGATACTA	10966
rs575364067	snp	G/T	0.00874735	0.0655527	intron-variant	RAB40B	GRCh38.p7	17:82674510	CGGGTGTGGTGGCGG[G/T]CACCTGTAGTCCCAG	10966
rs575408661	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82700578	CCATGTTCCAATCAG[C/T]TGTGGGTCACATGGC	10966
rs575417546	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82684749	CCTACAAAGAGGCTG[C/T]GGAAACTTCTGCGTG	10966
rs575420717	snp	C/G	0.000798403	0.0199641			GRCh38.p7	17:82654777	GCTGGTCTTGAACTC[C/G]TAAGCTCAGGCAATC	10966
rs575439085	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82686202	CTGAAACCTCCGCTT[C/T]CGGGGTTCAAGTGAT	10966
rs575499307	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82687474	TTCAGGAGCAAACTT[C/T]GCTGAGTCACATTAG	10966
rs575501280	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82667142	AAAAATGCGAGGCTG[C/T]GGAGGCCACGGTTCT	10966
rs575501967	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82673630	ACGTTCAGTCATTCC[A/G]GAGTTCCTTTTGAGA	10966
rs575540308	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82689880	GGCTGAGGCAGAGAA[C/T]TGCTTGGACCCAGGA	10966
rs575562117	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668835	GCCTGATCCGTGGAT[C/T]GAGAGGCCCAGCCAT	10966
rs575753890	snp	C/T	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82685799	AACAGGATCTCTTCT[C/T]CTTCTTCTTTTTTTT	10966
rs575778355	snp	A/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82676632	ACTAATTTTTCTTTT[A/T]CTTTTTCTTTTTTGA	10966
rs575837868	snp	A/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82677048	CCACCTCCCGGGTTC[A/T]AGCAATTCTCCTGCC	10966
rs575893188	snp	C/T	0.000399281	0.0141238			GRCh38.p7	17:82656348	TCCCTCATTTGCGAC[C/T]CCCAGCCACAGAGAA	10966
rs575934145	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82685475	AGAATGAGCTGTGTA[C/G]CCCGTAGGGTCCCAA	10966
rs575963751	in-del	-/CA	0.00676609	0.0577691	intron-variant	RAB40B	GRCh38.p7	17:82660274	ACATAAACAGGCAAG[-/CA]CACACGTACACATTA	10966
rs575991733	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82689928	ACCGAGATCGTGCCA[C/T]TGCACTCCAGCCTGG	10966
rs576054161	snp	A/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82690397	AAGGAGCATGGAGTG[A/T]GCACATGTGTTCTCA	10966
rs576186534	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699220	GCAGGCCGCCTCGCC[C/G]GAGGAGTCCCTGTCG	10966
rs576250230	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82693161	GTGCCCGCCACCACA[C/T]CTGGCTAATTTTTTT	10966
rs576301724	snp	A/G	0.00199481	0.0315187	intron-variant	RAB40B	GRCh38.p7	17:82687002	GAGCTCAGGGGTATC[A/G]AAGACCCTCCTGTCC	10966
rs576364310	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82691497	TCGAGACCAGCCTGA[C/T]CAACATGGTGAAACC	10966
rs576389964	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82684165	GGCAGGGGTTGCAGT[A/G]AGCCAAGATTGCGCT	10966
rs576441904	snp	A/C	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82688281	AAGTGCTGGGATTAC[A/C]GGTGTGAGCCACCAT	10966
rs576562825	in-del	-/T	0.499368	0.0177603			GRCh38.p7	17:82655951	GGTCCCTTAAATTTC[-/T]TTTTTTTTTTTTTTT	10966
rs576567734	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82662332	CCAAAAGCTATGGTC[C/G]AGGAGGCAGCGGGCC	10966
rs576573887	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82673706	CCTCCTGGTGGGCAT[A/G]GAGGCGCTTCTCTGA	10966
rs576641804	snp	A/C			intron-variant	RAB40B	GRCh38.p7	17:82674878	GGGAGTAGGCAGAGG[A/C]GAAAGAACAACACGA	10966
rs576646990	snp	C/T	0.0142736	0.0832652	intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671628	CTGACACAGCTCACC[C/T]CGTAACTCTAACACA	10966
rs576729728	snp	A/C	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82685952	GGGATTACAGGTGCC[A/C]GCCACCACACCCAGC	10966
rs576746922	snp	C/T	0.000798403	0.0199641			GRCh38.p7	17:82655432	CATTATCAGTAGTCC[C/T]GAGGAGACATCAATT	10966
rs576783813	snp	A/C	0.00438332	0.0466095	intron-variant	RAB40B	GRCh38.p7	17:82686257	GCTGAGATAACAGGC[A/C]CCTGCCACCACGCCC	10966
rs576826973	snp	G/T	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82660375	CACACGCACAGGCAC[G/T]CATGCACAGATGCAC	10966
rs576901767	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82684348	GACGGGGATGCAAAC[A/G]GTGTGGTCAGTGTGG	10966
rs576926603	snp	A/G	0.000798403	0.0199641			GRCh38.p7	17:82655195	AATATTTATTTTCTC[A/G]TAGCTCTGGAAGCCG	10966
rs576970492	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82664368	TGGGAGGGTGTTCCC[C/G]GGGGCGCTGTGCCGA	10966
rs576970590	snp	C/G	0.000798403	0.0199641	intron-variant	RAB40B	GRCh38.p7	17:82659512	CCTGGAGGGCCCGGC[C/G]CTAATTCCTGGCCTG	10966
rs576983086	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665095	CTCAGCTGTGTACAT[A/G]TGCATGTGAACCACG	10966
rs576985595	in-del	-/G	0.00954632	0.0684253	intron-variant	RAB40B	GRCh38.p7	17:82675823	CAGCACCCGAATTTG[-/G]GGGGGGTCACAAACA	10966
rs577008495	snp	C/T	0.00795532	0.062565	intron-variant	RAB40B	GRCh38.p7	17:82689734	AGCACTTTCGGAGGC[C/T]AAGGCGGGTGGATCA	10966
rs577032421	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82659901	CCCACGAGCCACTCC[A/G]GGAACACAGGATGCA	10966
rs577037376	snp	G/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82674503	AATTAGCCGGGTGTG[G/T]TGGCGGGCACCTGTA	10966
rs577100280	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668720	CTAAGCCTGCAGGGG[G/T]CAGGGGTGGCCTTCC	10966
rs577127796	snp	C/T	0.0103295	0.0711199	intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660903	TTGTCCTCCAATCAT[C/T]CATTAAAGGATGGTA	10966
rs577188665	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82691574	GTAATCCCAGCTACT[C/T]GGGGGGCTGAGGCAG	10966
rs577247019	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82663799	CGGTCCCCTCTTGGC[A/G]TCTTCCCACAGACAC	10966
rs577299134	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82670305	TTCTCGTGCCTCAGC[A/G]TCCCGTGTAGCTGGA	10966
rs577302722	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82664635	CGTTCAGGGAAGAAA[A/G]GGGTTTCTCATCAGT	10966
rs577330619	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82697591	GGTCGGCCTCGTCCA[A/G]GCTGTTCCAGGGATG	10966
rs577376970	snp	A/G	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669432	GTGAGCCGAGATCAC[A/G]CCATTTCACTCCAGC	10966
rs577641678	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82672899	AATTTTTGTTTCTAC[C/T]GGAGTTAAAAATTGC	10966
rs577658265	snp	A/C	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82674996	CCACATTCCTCTGTG[A/C]TGAAGCTATTTTGAG	10966
rs577678693	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699903	CAAGAAGAAGGATAA[C/T]GCCCCCACTACTTCA	10966
rs577777632	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82677470	GGCCCATCCTGCAGC[A/G]GCCAGCTCAACACAC	10966
rs577838011	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82684880	GAACTCTGGGAGGTC[A/G]AGGCGGGTGGATCAC	10966
rs577853182	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82691720	GCAAAAGGCAGAAAA[C/T]TCAGCACTCAGAGAA	10966
rs577872632	in-del	-/CA	0.00478085	0.0486577	intron-variant	RAB40B	GRCh38.p7	17:82660216	ACTCATGCACAGATG[-/CA]CACACAGTGCACACA	10966
rs577875011	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82663105	CCAACGCCAGCCCAG[C/T]GAGGGCATGGCCCCG	10966
rs577918094	snp	G/T			intron-variant	RAB40B	GRCh38.p7	17:82673836	ACTTTCTTGGATAAT[G/T]TGTTCTCTCCTTCTG	10966
rs577976593	snp	A/G	0.00119737	0.0244387	intron-variant	RAB40B	GRCh38.p7	17:82674209	GCCGGGTGTGGTGGC[A/G]GGTGCCTGTAATCCC	10966
rs577987518	snp	C/T	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82683553	ACCACTTTGGGAGGC[C/T]GAGGTAGGATGATCT	10966
rs578032958	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82684098	TGGTGGCAGGCACCT[C/G]TAATCCCAGCTACTC	10966
rs578115897	snp	A/T			intron-variant	RAB40B	GRCh38.p7	17:82689329	GTGCCAGGCTGGTGG[A/T]CAGGCTGGTGACAGG	10966
rs578151292	snp	A/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82658323	GGAGCTCCCTCATGA[A/G]CTTTCTGACAAAGCT	10966
rs578213424	snp	C/G	0.000399281	0.0141238	intron-variant	RAB40B	GRCh38.p7	17:82658773	GATTTTGTTGTCGTC[C/G]TAATGTGGGTGCTCT	10966
rs745620462	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82683311	AAAAGAAAAAAACTG[A/G]TCAACTGGATTTCTT	10966
rs745650407	snp	A/C			intron-variant	RAB40B	GRCh38.p7	17:82667559	TGGACTCCAGAGGCT[A/C]TTTCTGTGGTGCCAC	10966
rs745674575	snp	C/T			intron-variant, nc-transcript-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668255	TGGGGAAGTGCACGC[C/T]GATTGGTCCACAGGC	10966
rs745779307	snp	C/T	1.80562e-05	0.00300463	intron-variant, utr-variant-5-prime, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661087	AAGAAGAAACCAGTG[C/T]TTCTTCCTGACAACA	10966
rs745780623	snp	G/T			upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699557	CATCTGTGTGTCTGC[G/T]TGTGCATGTGTGCCT	10966
rs745869414	snp	G/T	1.64749e-05	0.00287005	missense	RAB40B	GRCh38.p7	17:82657933	CGGACGAGCTTCACT[G/T]TGCGGAGGCTGCTCC	10966
rs745976995	snp	A/C	1.65674e-05	0.00287809	splice-donor-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660986	GGGGATGCTGTGTTA[A/C]CTGTGCGCCCCGGGA	10966
rs746004859	in-del	-/GAATACACTTGGGAAT			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669981	CACGAGGCAATGAAC[-/GAATACACTTGGGAAT]CTATTTTCGAATGCG	10966
rs746123515	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82679663	CAGCATCAGGCTGGA[C/T]AAGTGCTGCAGAGGC	10966
rs746141997	in-del	-/AG			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671480	AACTCTAACACACAC[-/AG]TCACATGCTCCCTGT	10966
rs746161293	snp	C/T	2.23846e-05	0.00334542	missense, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698469	CCCGCCGGGTGGCCG[C/T]ACGGGGACTCGGCCG	10966
rs746167827	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82683292	CATTAAAAGGATGGT[C/T]TATAAAAGAAAAAAA	10966
rs746210467	snp	C/T					GRCh38.p7	17:82656312	ATCTGGGTATTTTCT[C/T]GCTTCGTTTTTTTGG	10966
rs746249936	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82674617	GCACTCCAGCCTGGG[C/G]GACAGAGCAAGACTC	10966
rs746251131	snp	A/G	1.76586e-05	0.00297136	synonymous-codon, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698545	TGTCGCCCACCAGCA[A/G]GAACTTGAGCAGAAA	10966
rs746258135	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82684360	AACGGTGTGGTCAGT[A/G]TGGAAAAGGGTTTGG	10966
rs746343606	snp	C/T	1.66529e-05	0.00288551	intron-variant	RAB40B	GRCh38.p7	17:82664601	TGAGGCTGCAGCTAA[C/T]AGGACGCTGGAAGTC	10966
rs746398880	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82660280	ACAGGCAAGCACACA[C/T]GTACACATTACACAC	10966
rs746497054	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82676666	GGAGTCTCGCTGTGT[C/T]GCCCAGGCTGGAATG	10966
rs746533822	snp	C/G	1.79725e-05	0.00299766	utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698635	CATGCCCGGCCTGCG[C/G]GGCTGAGCGCAGAGG	10966
rs746539378	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665015	AGACACTGAGACTGC[A/G]TCCCCCAGTATCACA	10966
rs746561193	snp	A/C	1.65822e-05	0.00287938	synonymous-codon	RAB40B	GRCh38.p7	17:82658582	GATGTTGAAATTGCA[A/C]AGAGGGCTGACCTCA	10966
rs746621971	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82694254	AAAAATTCAGGCCGC[A/G]CACTGTGGCTCACAC	10966
rs746640903	snp	A/G	1.64754e-05	0.00287009	missense	RAB40B	GRCh38.p7	17:82657925	GGGGGGGGCGGACGA[A/G]CTTCACTTTGCGGAG	10966
rs746716374	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82682618	ACTCCTCAAACTCAA[A/G]ACTTACTATATATTT	10966
rs746737780	snp	A/G	1.65795e-05	0.00287914	intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660974	TCTCCCAGCTCGGGG[A/G]ATGCTGTGTTACCTG	10966
rs746770745	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82658769	GTGAGATTTTGTTGT[C/T]GTCGTAATGTGGGTG	10966
rs746826996	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82659358	GTGGACGCTCGTTTC[A/G]TCTGGACCAGCTTCC	10966
rs746827771	snp	G/T	1.69395e-05	0.00291024	intron-variant, missense, downstream-variant-500B	RAB40B	GRCh38.p7	17:82661059	ATCCCTGGAAAAGAT[G/T]TTGGAGACCATTAAG	10966
rs746853513	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82687257	ATTTTATTAATCTAA[C/G]AGAAAATTTCATACT	10966
rs746895958	in-del	-/CAAAAAAAAAAAAA			intron-variant	RAB40B	GRCh38.p7	17:82681020	AGCAAGACTCCATCT[-/CAAAAAAAAAAAAA]AAAAAAAAAAAAAAA	10966
rs746970907	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82687994	AGAGGACTGTTTGAG[C/T]CCAGGAGGTCAAAGC	10966
rs746986779	in-del	-/AC			intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660690	TGCACACACATGTAC[-/AC]ACACACACACACACA	10966
rs747052044	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82670258	TGACGTGATCTCGCT[C/T]ACTGCAACCTCCGCC	10966
rs747115180	snp	A/T			intron-variant	RAB40B	GRCh38.p7	17:82681374	AGTTAGAAGCAGCCG[A/T]CTGGGAGAAGTCTCC	10966
rs747177423	snp	G/T	3.15482e-05	0.00397154	missense, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698457	CGCCCGCGCTCACCC[G/T]CCGGGTGGCCGTACG	10966
rs747201985	snp	C/T			upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699787	TCTAGAGAGCAAGGG[C/T]TGCCAGGCCGAGGTC	10966
rs747211013	snp	A/G	0.000117908	0.00767723	intron-variant	RAB40B	GRCh38.p7	17:82658139	CAAGCTCAGCACTTG[A/G]GAGAGAAAAGATAAA	10966
rs747235680	in-del	-/GA			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669136	TGAGCCCAGGAATTC[-/GA]AACCAGCCTGGGCAA	10966
rs747287626	in-del	-/C			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671789	CACTGACACAGCTCA[-/C]CCCGTAACTCTAACA	10966
rs747327278	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82659357	CGTGGACGCTCGTTT[C/T]GTCTGGACCAGCTTC	10966
rs747392607	snp	G/T			intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661331	ATACATTCAATGTAG[G/T]CTTTAAAAAACTTGT	10966
rs747394843	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82673938	TCTCTTTTTCCCAGC[A/G]TTCTGGGAATTCATC	10966
rs747401924	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82680111	TCCTCGGGCTGGCCC[A/G]TCCTGCTCAGACCGG	10966
rs747430486	snp	A/G	3.32027e-05	0.00407434	intron-variant	RAB40B	GRCh38.p7	17:82664589	ACGGCTTAGGCCTGA[A/G]GCTGCAGCTAACAGG	10966
rs747480650	snp	C/T			intron-variant, stop-gained	RAB40B	GRCh38.p7	17:82662470	CCTCCTGGGCCGCTG[C/T]CACCCTGAAGGAGCA	10966
rs747492668	in-del	-/AGGGA	1.65671e-05	0.00287807	intron-variant	RAB40B	GRCh38.p7	17:82659546	TCCTCCCAAGCCTAC[-/AGGGA]TCTTGGGCAGTGGCA	10966
rs747645268	snp	A/T					GRCh38.p7	17:82655551	CATCAGCGAGCTGGG[A/T]ACGGAGGGAGAAGAG	10966
rs747782623	snp	C/T	1.65551e-05	0.00287702	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657836	TTCTCCTGGAGAGAT[C/T]CCGCCGTGTTTCTTT	10966
rs747805895	in-del	-/CT			downstream-variant-500B	RAB40B	GRCh38.p7	17:82657006	GCAACAAGAGCGAAA[-/CT]CTGTCTCAAAAATAA	10966
rs747887347	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82684738	GGGAGGGGCTGCCTA[C/T]AAAGAGGCTGCGGAA	10966
rs747899908	in-del	-/CCTA	1.6821e-05	0.00290004	splice-donor-variant	RAB40B	GRCh38.p7	17:82658486	GGAATAGCCCCTGGG[-/CCTA]CCCTTGCTCGGCCGC	10966
rs748078930	snp	G/T			intron-variant	RAB40B	GRCh38.p7	17:82677703	TTCCAGGCACAGGTG[G/T]CCTGGCCCTACACAG	10966
rs748111604	snp	A/G	1.64768e-05	0.00287021	missense	RAB40B	GRCh38.p7	17:82658060	TTAAGGCAATGGGGA[A/G]CGGGAGCTTGTCCAC	10966
rs748173600	snp	C/T	9.94497e-05	0.00705088	intron-variant	RAB40B	GRCh38.p7	17:82664575	CGGAAGGGTTAGAGA[C/T]GGCTTAGGCCTGAGG	10966
rs748206511	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82674381	TCACGCCTGTAACCC[C/G]AGCACTTTGGGAGGC	10966
rs748223574	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668604	AAGTGTGGACCCACC[C/T]GGATGGTCTGCAGCA	10966
rs748247953	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669251	GAGGCCGAGCGGGGT[A/G]GATCACCTGAGGTCA	10966
rs748261484	snp	C/T	1.65784e-05	0.00287905	missense	RAB40B	GRCh38.p7	17:82658122	CGGCAGCAGAGGTCT[C/T]GCAAGCTCAGCACTT	10966
rs748441155	snp	G/T			intron-variant	RAB40B	GRCh38.p7	17:82687394	TTTTGCTTTTATTTT[G/T]AGTCAAACAAAATGC	10966
rs748516921	snp	A/G			intron-variant, missense	RAB40B	GRCh38.p7	17:82662603	TGGGGTCCACACTCC[A/G]GGGTCCACGGTGGGA	10966
rs748537178	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82663455	CCCAGAGCTGGAACC[A/G]CAGGAGCTCCCCCCA	10966
rs748558480	snp	A/T			intron-variant	RAB40B	GRCh38.p7	17:82672251	CTCACACGCTCCCTG[A/T]ACTCACTGACACACC	10966
rs748563194	in-del	-/G			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668393	GGTGTGGCTTCACCA[-/G]GGACCTGCCCCCTTC	10966
rs748589861	in-del	-/A			intron-variant	RAB40B	GRCh38.p7	17:82683807	AAGACCCTGTTTCCA[-/A]AAAAAAAAAAAAAAA	10966
rs748733077	snp	C/G/T	0.000308147	0.0124095	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657697	ATCCACGTAGAAATT[C/G/T]GAAGTCCGACGGGGT	10966
rs748742388	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82693848	AGCACTTTGGGAGGC[C/T]GAGGCGGGCAGATCA	10966
rs748764916	in-del	-/CTC	3.31455e-05	0.00407083	cds-indel	RAB40B	GRCh38.p7	17:82657823	GGTAACGCCGAGCTT[-/CTC]CTGGAGAGATTCCGC	10966
rs748773903	snp	G/T			intron-variant	RAB40B	GRCh38.p7	17:82672960	TGTAATCCCAGCACT[G/T]TGGGAGGTCAAGGCA	10966
rs748787752	snp	A/G			upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699240	AGTCCCTGTCGCCGT[A/G]GAATCCAGGCTCGCG	10966
rs748804861	in-del	-/GGGACT	1.73132e-05	0.00294216	cds-indel	RAB40B	GRCh38.p7	17:82658697	CCCACCAGGATCTTG[-/GGGACT]CCGGGGGCATGCTAG	10966
rs748833734	snp	C/T	1.65701e-05	0.00287833	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657825	TAACGCCGAGCTTCT[C/T]CTGGAGAGATTCCGC	10966
rs749016211	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82674227	TGCCTGTAATCCCAG[C/T]CACTCAGGAGGCTGA	10966
rs749021840	snp	G/T			intron-variant	RAB40B	GRCh38.p7	17:82677737	CCGCATCCTCTTTGC[G/T]CAGGACACTTGAAGT	10966
rs749069278	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82689266	ATGAGGCAGGACTGC[A/G]GGTCTGCCTGCTCCA	10966
rs749079194	in-del	-/TCTTTCTT			intron-variant	RAB40B	GRCh38.p7	17:82695176	TTACGAACGCCCTCA[-/TCTTTCTT]TCTTTCTTTCTTTCT	10966
rs749116918	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666408	CACCGCCACGTCCAG[C/T]TAATTTTTGTATTTT	10966
rs749212873	in-del	-/TT					GRCh38.p7	17:82655951	GGTCCCTTAAATTTC[-/TT]TTTTTTTTTTTTTTT	10966
rs749229381	snp	C/T	1.64743e-05	0.00287	synonymous-codon	RAB40B	GRCh38.p7	17:82658031	GGCCATCGAGAAGGA[C/T]TTGAGGTGGCTTCTT	10966
rs749286422	snp	C/T			downstream-variant-500B	RAB40B	GRCh38.p7	17:82656683	ATGTGATGTCTACAC[C/T]AGGCAGTGGCGCAGT	10966
rs749363528	snp	A/C	1.64751e-05	0.00287007	missense	RAB40B	GRCh38.p7	17:82657939	AGCTTCACTTTGCGG[A/C]GGCTGCTCCTTTTGT	10966
rs749417104	in-del	-/TT			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82670179	TGAGGGCCAACAATC[-/TT]TTTTTTTTTTTTTTT	10966
rs749420184	snp	C/T	1.65165e-05	0.00287367	missense, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82664517	TGCAGCTTCACCCGC[C/T]GCCCGTCCAGCAGGA	10966
rs749429493	in-del	-/TCAAAAAAAAAAAA			intron-variant	RAB40B	GRCh38.p7	17:82681019	GAGCAAGACTCCATC[-/TCAAAAAAAAAAAA]AAAAAAAAAAAAAAA	10966
rs749591374	snp	A/T	8.28205e-05	0.00643455	synonymous-codon	RAB40B	GRCh38.p7	17:82658564	CTCCGTGAACGACTC[A/T]GTGATGTTGAAATTG	10966
rs749615429	snp	C/T					GRCh38.p7	17:82655337	GCCAAGGCCTCCGGG[C/T]GGCCCGTGCATTCGG	10966
rs749642194	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82682321	ACTAGGTACAGTAGC[C/T]CCCAAACCATGAAAT	10966
rs749647926	snp	A/G					GRCh38.p7	17:82654608	AGGCTGGAGTGCAGT[A/G]GTGCAATCTCAGCTG	10966
rs749682029	snp	A/T			intron-variant	RAB40B	GRCh38.p7	17:82694768	CATGTGAGCCAGGGG[A/T]TGGTGGAATGACAGC	10966
rs749726426	in-del	-/G			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669135	TGAGCCCAGGAATTC[-/G]GAAACCAGCCTGGGC	10966
rs749785771	snp	A/G	1.83673e-05	0.0030304	missense, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698572	GAAAGTCGTAGGCCC[A/G]GACCGGGCTGCCCAG	10966
rs749846155	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82663741	ATCACTGAGCCAGGC[A/G]TGGGGGACCCAGGAG	10966
rs749903212	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82688298	GTGTGAGCCACCATG[C/G]CTGGCCCTCATGACC	10966
rs749933432	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82659333	ACCCCACGCATAGCC[A/G]AGGTACGCCGTGGAC	10966
rs749956936	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82687934	ATAATTAGCCGGGCA[C/T]GGTGGCATGCACCTA	10966
rs750050902	snp	C/T	1.64958e-05	0.00287187	synonymous-codon	RAB40B	GRCh38.p7	17:82658097	CACCGGCGTGCAGGA[C/T]ACGACCGCCCGGCAG	10966
rs750180556	in-del	-/AAAAAAAAAA			intron-variant	RAB40B	GRCh38.p7	17:82681025	GACTCCATCTCAAAA[-/AAAAAAAAAA]AAAAAAAAAAAAAAA	10966
rs750181653	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82693420	CAGAGACAGCCCCGT[A/G]CTGAGAGGGAAGATG	10966
rs750200354	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82681992	GAAAATATCCACTCT[C/T]ACCACTCCAATTCAA	10966
rs750230119	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82680859	ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA	10966
rs750243274	snp	C/T					GRCh38.p7	17:82654972	AATGACAAAGTTTCT[C/T]TAAGGTTTAATTTAT	10966
rs750275932	snp	C/T	2.08483e-05	0.00322858	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657728	AGTGTGTTTCCATCA[C/T]ACGGAAGGCGTCGCA	10966
rs750348603	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669066	AAAATAGCCAGGCAC[A/G]GTGGCTCACGCCTGT	10966
rs750372092	snp	A/C			intron-variant	RAB40B	GRCh38.p7	17:82696028	ACATGTGACACCATG[A/C]TCGGCTAATTTTTGT	10966
rs750392311	snp	C/T	3.30382e-05	0.00406423	missense, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82664514	AGCTGCAGCTTCACC[C/T]GCCGCCCGTCCAGCA	10966
rs750474990	snp	C/T			intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660770	ACGTGTACATGCACA[C/T]ACAGTCCCGTAAATG	10966
rs750485813	snp	A/G	7.03309e-05	0.00592963	synonymous-codon	RAB40B	GRCh38.p7	17:82658708	CTTGGGGACTCCGGG[A/G]GCATGCTAGCGGGCA	10966
rs750486067	in-del	-/G	2.41421e-05	0.00347425	frameshift-variant	RAB40B	GRCh38.p7	17:82657910	TTTTGGGGGGGCTCT[-/G]GGGGGGGCGGACGAG	10966
rs750520170	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82686653	GGTCCCCGCTTAGAG[C/G]CTGCCAAGGGAGCGT	10966
rs750611341	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82663053	CAAAGGCCCAGCTGG[C/T]GGAGGGTGGGGAGCA	10966
rs750625188	snp	A/C	5.0104e-05	0.00500494	utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698616	ACGGCCCGGCGCCCC[A/C]ACCCATGCCCGGCCT	10966
rs750673253	snp	G/T			intron-variant	RAB40B	GRCh38.p7	17:82682102	ACCAGATGACATTAC[G/T]ATACACACACACACG	10966
rs750690291	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671929	CACACTCACATGCTC[C/T]CTGTACCCACTGACA	10966
rs750727711	snp	C/T	1.67077e-05	0.00289026	missense	RAB40B	GRCh38.p7	17:82658623	CGCCCAGGCGCTCGG[C/T]GTAGGCCTGGGCCTG	10966
rs750751052	in-del	-/ACTC			intron-variant	RAB40B	GRCh38.p7	17:82672252	TCACACGCTCCCTGT[-/ACTC]ACTGACACACCCCAC	10966
rs750932758	snp	G/T	3.30666e-05	0.00406598	missense	RAB40B	GRCh38.p7	17:82657904	TGCAGTTTTTGGGGG[G/T]GCTCTGGGGGGGGCG	10966
rs751051928	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669929	TAATAGCAATCCTCA[A/G]AGAGAATTTTGGAAA	10966
rs751077661	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82688826	GTAATCCCAGCTACT[C/G]AGGACACTGAGGCAG	10966
rs751094083	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82677649	TTCCAATCCTCGTCC[A/G]CCACCCGTCTCCAGG	10966
rs751137154	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82678254	ATCAGCAGTGTTAGC[A/G]TTAGGATAATACAAT	10966
rs751227091	snp	C/T	4.94189e-05	0.00497062	missense	RAB40B	GRCh38.p7	17:82658000	CGCCGTGCATCATCC[C/T]GGCATTCAGGCCGTT	10966
rs751252182	snp	A/C			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668598	TGCCCCAAGTGTGGA[A/C]CCACCCGGATGGTCT	10966
rs751265313	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82691082	GGGCCAGGCCCTGCA[C/T]CTGCACCCCGGTGTG	10966
rs751268649	snp	C/G			intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660953	TATTATTCAAAGTTG[C/G]TTTGATCTCCCAGCT	10966
rs751346803	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82682862	ATTAAAAAACGAACC[C/T]GGCCGGGCACGGTGA	10966
rs751467882	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82670649	AAGGGATTCTCCTGT[C/T]TCAGCCTCCTGAGTA	10966
rs751484476	in-del	-/A	1.64749e-05	0.00287005	frameshift-variant	RAB40B	GRCh38.p7	17:82657966	TGTGGGTGGAGCTGG[-/A]TGGTGAGGGAGTAGG	10966
rs751497719	snp	A/G	1.66746e-05	0.00288739	missense	RAB40B	GRCh38.p7	17:82658613	AAGAAGGTCACGCCC[A/G]GGCGCTCGGCGTAGG	10966
rs751500561	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82678757	CAGCACAGGGCTCCT[A/G]GAAGTGGCCGGTGCT	10966
rs751546246	in-del	-/GCGGGACGCTC	0.000970159	0.0220031	intron-variant	RAB40B	GRCh38.p7	17:82664466	TTACTCCCTGGGGGT[-/GCGGGACGCTC]GCACCTCCTCCAGAC	10966
rs751591971	snp	A/G	0.000126207	0.00794276	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657658	CCTTTACAAACACAC[A/G]TCGAAAACAAGAGCT	10966
rs751669671	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82663238	TGGCCACTACTAGAC[A/G]GGGCAGGCGTAGGAA	10966
rs751673962	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82676136	CTCGTGGGACGCACT[C/T]ACCACAGCTCCTCAA	10966
rs751700266	snp	C/T	3.31367e-05	0.00407029	synonymous-codon	RAB40B	GRCh38.p7	17:82658540	CCGCAGCAGCACGAT[C/T]CTGGCCAGCTCCGTG	10966
rs751754802	snp	A/C					GRCh38.p7	17:82655173	AAACCTGGTGACTTA[A/C]ATAACAAATATTTAT	10966
rs751768948	snp	A/C/G	8.24567e-05	0.0064205	missense	RAB40B	GRCh38.p7	17:82657913	TGGGGGGGCTCTGGG[A/C/G]GGGGCGGACGAGCTT	10966
rs751818585	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82682558	AGAAATCAACAAAGC[C/T]AACATTTAAAAGGAA	10966
rs751823594	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82682082	AGATTAAAACCATCT[C/T]GATTACCAGATGACA	10966
rs751871099	snp	C/T	1.7683e-05	0.00297341	missense, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698533	TGCCCACGTCGCTGT[C/T]GCCCACCAGCAGGAA	10966
rs752075833	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82675303	CCCATTAGCACAGCC[C/T]GGATGCATAACCCAC	10966
rs752223986	in-del	-/CACCTGCCACCA			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666032	ATAGGCACACCACTG[-/CACCTGCCACCA]CACCTGCCACCACAC	10966
rs752263087	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82667071	ACGGCCTCTGCAGCT[C/G]TCCTTCCAGAGAAGC	10966
rs752263317	snp	A/G/T	8.32807e-05	0.00645249	intron-variant	RAB40B	GRCh38.p7	17:82664473	CTGGGGGTGCGGGAC[A/G/T]CTCGCACCTCCTCCA	10966
rs752306286	snp	A/G			utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657400	CTCTACATCTGCAGC[A/G]TTTTATAAATTGGCG	10966
rs752360621	snp	C/T	1.66217e-05	0.0028828	synonymous-codon, downstream-variant-500B	RAB40B	GRCh38.p7	17:82661038	AAATCTTCCCTGGCC[C/T]GAAGTATCCCTGGAA	10966
rs752404032	in-del	-/CCC			intron-variant	RAB40B	GRCh38.p7	17:82676304	CACCTTCAACAGCCT[-/CCC]CTCCCTCCACACAGT	10966
rs752500674	in-del	-/C	3.31532e-05	0.0040713	intron-variant	RAB40B	GRCh38.p7	17:82664578	AAGGGTTAGAGACGG[-/C]TTAGGCCTGAGGCTG	10966
rs752578342	snp	C/T			intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661814	ATTGTTTGAGCCCGG[C/T]AGGCGGAGGTTGCAG	10966
rs752599046	in-del	-/G			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666433	ATTTTTAGTAGAGAT[-/G]GGGGTTTCATCATAT	10966
rs752620492	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82658856	CCTCGTTTGGAAAGA[C/G]CGTCTTTGCAGACGT	10966
rs752650319	snp	A/G	1.70151e-05	0.00291672	intron-variant	RAB40B	GRCh38.p7	17:82658456	CTCGGCATCTGGAGG[A/G]CAGAGGTGGCCCCCG	10966
rs752693808	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665466	GCTATGTTTCCCAGG[C/T]TGGTCTCAAACGCCT	10966
rs752726237	snp	G/T			intron-variant	RAB40B	GRCh38.p7	17:82690325	ACGGAGTGTGCATGT[G/T]TGTTCCTGGGAGCAG	10966
rs752740170	snp	C/T	1.65864e-05	0.00287974	synonymous-codon	RAB40B	GRCh38.p7	17:82658531	CATCCCATGCCGCAG[C/T]AGCACGATCCTGGCC	10966
rs752844659	snp	A/G	4.27068e-05	0.00462077	intron-variant	RAB40B	GRCh38.p7	17:82698449	ACGCCCTCCGCCCGC[A/G]CTCACCCGCCGGGTG	10966
rs752874827	snp	C/G/T	3.31952e-05	0.0040739	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657813	AGCTGCCGGGGGTAA[C/G/T]GCCGAGCTTCTCCTG	10966
rs752962837	snp	A/T	1.65302e-05	0.00287486	missense	RAB40B	GRCh38.p7	17:82657897	TTTCTGGTGCAGTTT[A/T]TGGGGGGGCTCTGGG	10966
rs753006932	in-del	-/AAAC			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665215	ATTTTTTCAAGTTAA[-/AAAC]AAACAAACAAAAAAA	10966
rs753016754	snp	A/G	1.64985e-05	0.0028721	stop-gained	RAB40B	GRCh38.p7	17:82659603	TCTCCTTAATCCATC[A/G]ATCAATGCCGTCAAA	10966
rs753292137	snp	A/G					GRCh38.p7	17:82654976	ACAAAGTTTCTCTAA[A/G]GTTTAATTTATATTT	10966
rs753313655	snp	A/G	1.92695e-05	0.00310393	intron-variant	RAB40B	GRCh38.p7	17:82658734	GGGCAGGAGAAAGGC[A/G]AGGAGCATGGGTTAC	10966
rs753378772	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82659158	CAGGTTGTGGTCGTC[A/G]GTTCTAGCAGCCCCG	10966
rs753400070	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668889	GGCAGCAGCCACTCT[A/G]GATGGGCCACTGCTA	10966
rs753403115	in-del	-/ACTA			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671441	ACACACGCTCCCTGT[-/ACTA]ACTGACACACCCCAC	10966
rs753476862	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82674197	AATACAAAATTAGCC[A/G]GGTGTGGTGGCGGGT	10966
rs753599028	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82690592	GCAGAGAGTGTGCAC[A/G]TGTGTCCAGGGGAAG	10966
rs753605400	snp	A/G			intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82662343	GGTCGAGGAGGCAGC[A/G]GGCCAGGTCAATCTG	10966
rs753625175	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82672674	GCGATGCCCTCTGCC[A/G]GGTTATGACGCAGCA	10966
rs753683427	snp	C/G	1.70443e-05	0.00291923	intron-variant	RAB40B	GRCh38.p7	17:82658445	CGCTGACCCACCTCG[C/G]CATCTGGAGGGCAGA	10966
rs753856762	snp	A/C/G			intron-variant	RAB40B	GRCh38.p7	17:82684336	TCACACACTGCTGAC[A/C/G]GGGATGCAAACGGTG	10966
rs753877226	snp	A/G	3.32281e-05	0.0040759	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657805	CATCCACCAGCTGCC[A/G]GGGGTAACGCCGAGC	10966
rs753880778	snp	A/G	0.000211595	0.0102836	intron-variant	RAB40B	GRCh38.p7	17:82698436	CCCGCACCCCGGCAC[A/G]CCCTCCGCCCGCGCT	10966
rs753915099	snp	C/G			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671509	GTACTCACTGACACA[C/G]CCCACCCCTGTAACT	10966
rs754018112	snp	A/G			intron-variant, synonymous-codon, downstream-variant-500B	RAB40B	GRCh38.p7	17:82661050	GCCTGAAGTATCCCT[A/G]GAAAAGATGTTGGAG	10966
rs754028628	snp	G/T	1.83092e-05	0.0030256	intron-variant	RAB40B	GRCh38.p7	17:82658721	GGGGCATGCTAGCGG[G/T]CAGGAGAAAGGCGAG	10966
rs754049600	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82673617	TTTTCCCTTAAACAC[A/G]TTCAGTCATTCCAGA	10966
rs754102475	in-del	-/TTA			intron-variant	RAB40B	GRCh38.p7	17:82679260	ACACCACAAGCCTTA[-/TTA]TTATTATTATTATTA	10966
rs754118602	snp	C/T	4.95511e-05	0.00497726	intron-variant	RAB40B	GRCh38.p7	17:82659572	GCAGTGGCATTTCTA[C/T]AACATACCTCATCGA	10966
rs754144952	snp	C/T			intron-variant, downstream-variant-500B	RAB40B, MIR4525	GRCh38.p7	17:82667784	CACCCGCTTTGCAGA[C/T]GCCACCTGCCCCGTG	10966
rs754155710	snp	C/G	1.8968e-05	0.00307955	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657735	TTCCATCACACGGAA[C/G]GCGTCGCACACATTC	10966
rs754237370	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665548	CATAAGCCACCATGC[C/T]GGAACACTTCTTCTA	10966
rs754296086	snp	A/C			intron-variant	RAB40B	GRCh38.p7	17:82695159	GGAAATGGAGTGTGG[A/C]GTTACGAACGCCCTC	10966
rs754325657	snp	C/T					GRCh38.p7	17:82656097	GGGATTACAGGTGTG[C/T]GCTGCCATGCCAAGC	10966
rs754329781	snp	A/G	1.64735e-05	0.00286993	synonymous-codon	RAB40B	GRCh38.p7	17:82657986	GAGGGAGTAGGAACC[A/G]CCGTGCATCATCCTG	10966
rs754343258	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665438	TTGTATTTTTTTGTA[A/G]AGACGGGGTTTCGCT	10966
rs754420418	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82695951	GTGCGATCTCTGCAA[C/T]CTCCGCCTCCCGGGT	10966
rs754487239	in-del	AAAAAAAAAAAAAAA/G			intron-variant	RAB40B	GRCh38.p7	17:82681033	TCAAAAAAAAAAAAA[AAAAAAAAAAAAAAA/G]AAGAAAGAGAAAAGA	10966
rs754495699	snp	A/G	3.31395e-05	0.00407046	missense, downstream-variant-500B	RAB40B	GRCh38.p7	17:82661018	TAGGAGCGGAATATG[A/G]TACAAAATCTTCCCT	10966
rs754502118	snp	A/C	1.66081e-05	0.00288163	intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660960	CAAAGTTGGTTTGAT[A/C]TCCCAGCTCGGGGGA	10966
rs754586216	snp	A/C/G	9.92382e-05	0.00704346	missense, synonymous-codon	RAB40B	GRCh38.p7	17:82657905	GCAGTTTTTGGGGGG[A/C/G]CTCTGGGGGGGGCGG	10966
rs754610666	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668765	CACAGAGACGCCCGC[A/G]TCTAGAGCTGCCCCA	10966
rs754685283	snp	A/G					GRCh38.p7	17:82656318	GTATTTTCTCGCTTC[A/G]TTTTTTTGGTTTAGT	10966
rs754746279	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82670005	TGGGAATCTATTTTC[A/G]AATGCGGAGATAACT	10966
rs754802964	in-del	-/AGG			intron-variant	RAB40B	GRCh38.p7	17:82688521	CAGGAGGCTTGAGGC[-/AGG]AGGAGAAGTGCTTGA	10966
rs754818250	in-del	-/C	1.69818e-05	0.00291387	intron-variant	RAB40B	GRCh38.p7	17:82658466	GGAGGGCAGAGGTGG[-/C]CCCCGGAATAGCCCC	10966
rs754941534	in-del	-/GTA	1.65168e-05	0.00287369	cds-indel	RAB40B	GRCh38.p7	17:82664546	GATGGTGGTCGTCTT[-/GTA]GTCGATGCCTGCGGA	10966
rs754949502	snp	A/G	6.60928e-05	0.00574822	synonymous-codon	RAB40B	GRCh38.p7	17:82658112	CACGACCGCCCGGCA[A/G]CAGAGGTCTTGCAAG	10966
rs754971340	snp	A/C	5.15663e-05	0.00507745	intron-variant	RAB40B	GRCh38.p7	17:82698446	GGCACGCCCTCCGCC[A/C]GCGCTCACCCGCCGG	10966
rs755035591	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82672966	CCCAGCACTTTGGGA[A/G]GTCAAGGCAGGTGGA	10966
rs755050441	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82693799	TCACAGAAGTGCACA[C/T]TGGCCAGGCGCAGTG	10966
rs755050952	snp	C/T	0.000116708	0.0076381	intron-variant	RAB40B	GRCh38.p7	17:82664606	CTGCAGCTAACAGGA[C/T]GCTGGAAGTCTCACG	10966
rs755174850	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82682090	ACCATCTCGATTACC[A/G]GATGACATTACTATA	10966
rs755179029	snp	C/T	1.8745e-05	0.0030614	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657737	CCATCACACGGAAGG[C/T]GTCGCACACATTCGC	10966
rs755264485	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82682863	TTAAAAAACGAACCC[A/G]GCCGGGCACGGTGAC	10966
rs755275326	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82684668	CTGAGTGACCGGAGC[C/T]AGGTTCAAAGGCCTC	10966
rs755297557	snp	C/G	3.3865e-05	0.00411477	missense	RAB40B	GRCh38.p7	17:82658643	GCCTGGGCCTGCTCC[C/G]TGGGCACCTGCCGCT	10966
rs755397268	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82682584	AGGAAAGTCAAAAGA[A/G]CAAAGTTGGAAGACT	10966
rs755414634	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82675304	CCATTAGCACAGCCC[A/G]GATGCATAACCCACA	10966
rs755455088	snp	C/T	3.56259e-05	0.00422039	utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698631	CACCCATGCCCGGCC[C/T]GCGGGGCTGAGCGCA	10966
rs755731742	snp	A/G	3.29935e-05	0.00406149	missense	RAB40B	GRCh38.p7	17:82659627	CGTCAAAAGACCAGC[A/G]GTTCGCAATGTCATA	10966
rs755761143	snp	C/T			intron-variant, downstream-variant-500B, utr-variant-5-prime	RAB40B, MIR4525	GRCh38.p7	17:82668061	GGAGGGTGAGCGAGA[C/T]GAGGAGGAGCTTTAC	10966
rs755767102	in-del	-/CGGTTCCC	1.69533e-05	0.00291142	frameshift-variant	RAB40B	GRCh38.p7	17:82658676	AACGCCAGGTGCAGG[-/CGGTTCCC]CACCAGGATCTTGGG	10966
rs755867641	snp	C/T	8.23662e-05	0.00641688	synonymous-codon	RAB40B	GRCh38.p7	17:82658022	CAGGCCGTTGGCCAT[C/T]GAGAAGGACTTGAGG	10966
rs755880538	in-del	-/AAAA			intron-variant	RAB40B	GRCh38.p7	17:82694664	GAAGAACTATGAGAC[-/AAAA]AGAAAGAATTCCTCA	10966
rs755890112	in-del	-/C	1.83922e-05	0.00303245	frameshift-variant, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698575	AGTCGTAGGCCCGGA[-/C]CGGGCTGCCCAGGGC	10966
rs755955648	snp	C/T	1.6498e-05	0.00287206	missense	RAB40B	GRCh38.p7	17:82658099	CCGGCGTGCAGGACA[C/T]GACCGCCCGGCAGCA	10966
rs756019515	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82689006	CCCAAGCCCTTTGGA[C/T]GCTGTTGTTCTTTTC	10966
rs756104311	snp	A/T	5.35547e-05	0.00517441	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657695	ACATCCACGTAGAAA[A/T]TCGAAGTCCGACGGG	10966
rs756171149	snp	C/T	7.22896e-05	0.00601162	intron-variant	RAB40B	GRCh38.p7	17:82658718	CCGGGGGCATGCTAG[C/T]GGGCAGGAGAAAGGC	10966
rs756178097	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82674413	AAGGTGGGCGGATCA[C/T]GAGGTCAGGAGTTCG	10966
rs756265057	snp	C/T	0.000121879	0.00780544	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657730	TGTGTTTCCATCACA[C/T]GGAAGGCGTCGCACA	10966
rs756293272	snp	C/G			upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699752	GGTGGGACCCTCCAG[C/G]CTTTTGGCTTCTCCT	10966
rs756298236	snp	A/G	1.67683e-05	0.00289549	missense	RAB40B	GRCh38.p7	17:82658634	TCGGCGTAGGCCTGG[A/G]CCTGCTCCGTGGGCA	10966
rs756376761	in-del	-/AC			intron-variant	RAB40B	GRCh38.p7	17:82660078	ACACATGTTGCATAC[-/AC]ACACGCAGGCACTCA	10966
rs756384225	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82676503	ACACCAATTCCGTGG[C/T]GAGTCTCTCGGCTCT	10966
rs756442024	snp	A/G	1.77037e-05	0.00297515	synonymous-codon, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698552	CACCAGCAGGAACTT[A/G]AGCAGAAAGTCGTAG	10966
rs756467479	in-del	-/ACTACAC			intron-variant	RAB40B	GRCh38.p7	17:82693386	GAAATGCAAAGGCAA[-/ACTACAC]ACCACAGAAGGACAG	10966
rs756490990	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82663625	CCCCAGGCTGGCCAG[C/G]AAGTCCTCACCTCCC	10966
rs756532060	snp	C/T	2.65213e-05	0.00364142	utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698619	GCCCGGCGCCCCCAC[C/T]CATGCCCGGCCTGCG	10966
rs756543595	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82664774	AGCCGCCTTGGCCTC[C/T]GTGGGGGTCAGGCTC	10966
rs756546127	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82684922	AGTTCGAGACCAGCC[C/T]GGCCAATATGGCAAA	10966
rs756563531	snp	A/G	1.6563e-05	0.00287771	missense	RAB40B	GRCh38.p7	17:82658559	GCCAGCTCCGTGAAC[A/G]ACTCTGTGATGTTGA	10966
rs756570355	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82693956	GGCGTGGTGGCGCAC[A/G]CCTGTAGTCCCAGCT	10966
rs756712740	snp	A/C			intron-variant	RAB40B	GRCh38.p7	17:82686378	CGGCCTCCCAAAGTG[A/C]TGGGATTATAGGCAT	10966
rs756767431	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668952	CACCACAGTGGGGCA[C/T]GCGGCGTAGCCTCCA	10966
rs756820028	snp	A/T			intron-variant	RAB40B	GRCh38.p7	17:82659160	GGTTGTGGTCGTCGG[A/T]TCTAGCAGCCCCGGG	10966
rs756865079	in-del	-/ACCTGTGCAGCG			intron-variant	RAB40B	GRCh38.p7	17:82667436	GCCTGATCTGAGCAC[-/ACCTGTGCAGCG]CCTTCCATGAGATCC	10966
rs756895536	snp	C/G	1.64732e-05	0.0028699	synonymous-codon	RAB40B	GRCh38.p7	17:82658007	CATCATCCTGGCATT[C/G]AGGCCGTTGGCCATC	10966
rs757037768	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82672737	TGGACTTCCCAGCCT[C/T]CAGAACTGTAAGAAA	10966
rs757132162	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82693656	CACCCAAATGCCCGT[C/T]ACCCGCAGGATGGAG	10966
rs757238613	snp	C/T			upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699468	ACATCTATGTGTCTG[C/T]GTGTGCATGTGTCCC	10966
rs757259866	snp	C/T	0.000123939	0.00787109	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657660	TTTACAAACACACAT[C/T]GAAAACAAGAGCTTC	10966
rs757304772	in-del	-/CAAAAAAAAA			intron-variant	RAB40B	GRCh38.p7	17:82681020	AGCAAGACTCCATCT[-/CAAAAAAAAA]AAAAAAAAAAAAAAA	10966
rs757314831	snp	A/G			utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657592	TGCAATCATGATAAA[A/G]TAACATTCAGAATTT	10966
rs757328406	snp	C/T			intron-variant, downstream-variant-500B, utr-variant-5-prime	RAB40B, MIR4525	GRCh38.p7	17:82668194	CGCAGCTGGTCATCC[C/T]GACGTCCGCGTTGCT	10966
rs757341805	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82658917	GGGCCCTCATCTAAT[A/G]ACTGGTGTCCTTGGG	10966
rs757394847	snp	C/T	6.67278e-05	0.00577577	missense	RAB40B	GRCh38.p7	17:82658616	AAGGTCACGCCCAGG[C/T]GCTCGGCGTAGGCCT	10966
rs757421185	snp	G/T	1.76774e-05	0.00297294	synonymous-codon, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698534	GCCCACGTCGCTGTC[G/T]CCCACCAGCAGGAAC	10966
rs757436535	snp	C/T			intron-variant, utr-variant-5-prime, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661163	AGTCAGCAGCCACCA[C/T]GCCGCCAGCGTGAGA	10966
rs757482304	snp	A/G			intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82662378	CTTCGCAGGGAGGCC[A/G]AAGGGCCAGCACGTG	10966
rs757498216	in-del	-/T			intron-variant	RAB40B	GRCh38.p7	17:82676495	TCACCCACACACCAA[-/T]TCCGTGGCGAGTCTC	10966
rs757597177	snp	A/G					GRCh38.p7	17:82656151	ACGGGGTTTCATCAC[A/G]TTGGCCAGACTGGTC	10966
rs757641492	snp	C/T			intron-variant, downstream-variant-500B, synonymous-codon	RAB40B, MIR4525	GRCh38.p7	17:82667908	GCACGCTGAGTGCAC[C/T]GTCTGTCTCTCTCTT	10966
rs757689551	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82683068	GAATTGCTTGAATCC[A/G]GGAGATGGAGCTTGC	10966
rs757694126	snp	C/T	2.91286e-05	0.00381621	synonymous-codon, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698459	CCCGCGCTCACCCGC[C/T]GGGTGGCCGTACGGG	10966
rs757729573	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82695169	TGTGGAGTTACGAAC[A/G]CCCTCATCTTTCTTT	10966
rs757781084	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82696150	CGGGATTACAGGTGT[A/G]AGCCACCGCCCCCGG	10966
rs757876031	snp	C/T	4.94572e-05	0.00497254	missense	RAB40B	GRCh38.p7	17:82657918	GGGCTCTGGGGGGGG[C/T]GGACGAGCTTCACTT	10966
rs758025636	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82676587	TTGAGGCTTACCCCC[A/G]CCAGTTTGACATCTC	10966
rs758047618	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82688772	AACCCCGTCTTTACT[A/G]AAAATACAAAAATTA	10966
rs758115562	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82677571	CCATCAGCCCTGACG[C/T]CGCGTCTCTGTCCCT	10966
rs758156664	snp	A/G			utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657122	CATTTTCCTAAATAA[A/G]TGTTTTCACTTCATT	10966
rs758157361	in-del	-/C			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666587	TTTCCCCGCCCCCAT[-/C]CACCCCCCAGACACC	10966
rs758284279	in-del	-/CACACAGTGAGGGCACCCCTCACCTTCAACAGCCTCTCCCTC			intron-variant	RAB40B	GRCh38.p7	17:82676270	ACAGCATCTCCCCCA[lengthTooLong]CACACAGTGAGGGCA	10966
rs758404548	snp	C/T	1.65751e-05	0.00287876	missense	RAB40B	GRCh38.p7	17:82658536	CATGCCGCAGCAGCA[C/T]GATCCTGGCCAGCTC	10966
rs758446800	snp	A/G			intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82662412	TCAGAGTGCCCCATC[A/G]TGAAGTGGGAGCACT	10966
rs758484171	in-del	-/A			intron-variant	RAB40B	GRCh38.p7	17:82681897	TGCATCTTAAAAAAA[-/A]GAACCTCAAAGCTAA	10966
rs758485165	in-del	-/ACAC			intron-variant	RAB40B	GRCh38.p7	17:82682105	AGATGACATTACTAT[-/ACAC]ACACACACGCATGCA	10966
rs758511174	snp	C/T	3.35362e-05	0.00409475	missense, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698455	TCCGCCCGCGCTCAC[C/T]CGCCGGGTGGCCGTA	10966
rs758599740	snp	C/T	1.78376e-05	0.00298638	missense, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698515	TCGCCAGGATCTCGC[C/T]CTTGCCCACGTCGCT	10966
rs758599960	snp	A/G	6.7944e-05	0.00582816	intron-variant	RAB40B	GRCh38.p7	17:82658464	CTGGAGGGCAGAGGT[A/G]GCCCCCGGAATAGCC	10966
rs758625884	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82693505	GCGAGAATCTACTAC[A/G]GGGAAACCTGTGCAG	10966
rs758831863	snp	A/G	3.87574e-05	0.00440196	intron-variant	RAB40B	GRCh38.p7	17:82658737	CAGGAGAAAGGCGAG[A/G]AGCATGGGTTACTTC	10966
rs758986893	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82662782	TGAGGGTGACTGTTC[A/G]GCCCACTGGGCAGCT	10966
rs759040689	snp	A/T			intron-variant	RAB40B	GRCh38.p7	17:82673907	CCCACCTTTCTTGTC[A/T]GATTTTGCATCTCTC	10966
rs759097175	snp	C/G	0.000116452	0.00762971	synonymous-codon	RAB40B	GRCh38.p7	17:82658603	GCTGACCTCAAAGAA[C/G]GTCACGCCCAGGCGC	10966
rs759119048	snp	A/G	0.000153674	0.00876431	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657708	AATTCGAAGTCCGAC[A/G]GGGTAGTGTGTTTCC	10966
rs759172734	snp	G/T			intron-variant	RAB40B	GRCh38.p7	17:82680612	CGATTAATATTTCAG[G/T]GTAGTTCATTTCACT	10966
rs759274043	snp	G/T			intron-variant	RAB40B	GRCh38.p7	17:82683591	CCAGGATCTCTTGAG[G/T]ATCTCTCAAGGGCAG	10966
rs759399008	snp	A/G			downstream-variant-500B	RAB40B	GRCh38.p7	17:82656915	GCTACTCGGGAGGCT[A/G]AGGCAGGAGAATCGC	10966
rs759416119	snp	A/G/T	1.6591e-05	0.00288015	synonymous-codon, missense	RAB40B	GRCh38.p7	17:82658527	GGTCCATCCCATGCC[A/G/T]CAGCAGCACGATCCT	10966
rs759442334	snp	A/G	2.01278e-05	0.0031723	missense, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698595	CTGCCCAGGGCGCTC[A/G]TCGTGACGGCCCGGC	10966
rs759471997	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82677407	TCACTGGTTTCTCCC[A/G]TCCCAACAGGGCAGA	10966
rs759500642	snp	A/G	0.000143128	0.00845834	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657705	AGAAATTCGAAGTCC[A/G]ACGGGGTAGTGTGTT	10966
rs759523500	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82673071	TAGCCAGGCATGGTG[A/G]TGGGCGCCTGTAGTC	10966
rs759554153	snp	A/T	3.30587e-05	0.00406549	intron-variant	RAB40B	GRCh38.p7	17:82659678	GGAGAGGTCACAGGC[A/T]CAGCACGCAGAACAC	10966
rs759642032	snp	A/G	1.65261e-05	0.0028745	missense	RAB40B	GRCh38.p7	17:82657877	CTTAAGAAATTTTGC[A/G]GCTGTTTCTGGTGCA	10966
rs759671688	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665125	GCATGTGCAGGGACA[C/T]GGGACTGCACACCCG	10966
rs759749362	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82659122	ACCGTGAGAGAATGC[A/G]TTTCTGTTGTTCAGG	10966
rs759873386	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82695670	GATCTGCAATCACAC[C/T]ACTGCACTCCAGCCT	10966
rs759875355	snp	C/G			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669519	TTGGCCAATCATGGT[C/G]GTGCACACCTGTCGT	10966
rs759883897	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666571	TTAAAGGGAAAAATA[C/T]GTTTCCCCGCCCCCA	10966
rs760073527	snp	C/G	1.64846e-05	0.0028709	missense	RAB40B	GRCh38.p7	17:82658084	TGTCCACCAGGTGCA[C/G]CGGCGTGCAGGACAC	10966
rs760122122	snp	A/G	1.66885e-05	0.00288859	missense	RAB40B	GRCh38.p7	17:82658503	TACCCTTGCTCGGCC[A/G]CCAGAGCCGGTCCAT	10966
rs760125823	snp	G/T			intron-variant	RAB40B	GRCh38.p7	17:82673872	TGATTAATCAGATAC[G/T]GGGCCTCCTGAGCCT	10966
rs760204709	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82674889	GAGGAGAAAGAACAA[C/T]ACGAGATAATCCTGA	10966
rs760240396	snp	C/G	1.93104e-05	0.00310722	missense, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698484	TACGGGGACTCGGCC[C/G]CGCCATCCTGCAGGC	10966
rs760299386	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668829	GCTGCTGCCTGATCC[A/G]TGGATCGAGAGGCCC	10966
rs760451932	snp	C/G	4.96159e-05	0.00498051	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657852	CCGCCGTGTTTCTTT[C/G]AGTGCCTTCCTTAAG	10966
rs760490139	snp	A/G			intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82662102	GATGAGCGGTGGGAC[A/G]CGGCATGGTTTTGCT	10966
rs760524386	snp	C/G	1.6631e-05	0.00288362	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657800	AGATGCATCCACCAG[C/G]TGCCGGGGGTAACGC	10966
rs760534079	in-del	-/TTT			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82670535	TAAAAGAATTCCTGA[-/TTT]TTTTTTTTTTTTTTT	10966
rs760594436	snp	G/T	1.651e-05	0.0028731	intron-variant	RAB40B	GRCh38.p7	17:82659666	TCACACCCTGGGGGA[G/T]AGGTCACAGGCTCAG	10966
rs760597875	snp	A/C			intron-variant	RAB40B	GRCh38.p7	17:82660264	ACATGCATGCACATA[A/C]ACAGGCAAGCACACA	10966
rs760608083	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666685	TGTCATTGAGAACAT[A/G]GAAAGAGAGGGTTTG	10966
rs760651675	snp	A/C			intron-variant	RAB40B	GRCh38.p7	17:82662828	TTCGCTAAGGTGAGC[A/C]GCCAGACCCGGGGTG	10966
rs760690989	snp	A/C			intron-variant	RAB40B	GRCh38.p7	17:82691537	ACTAAAAATACAAAA[A/C]TTAGCCGGGCATGGT	10966
rs760786454	snp	A/G	1.65581e-05	0.00287728	intron-variant	RAB40B	GRCh38.p7	17:82659549	TCCCAAGCCTACAGG[A/G]ATCTTGGGCAGTGGC	10966
rs760863252	snp	C/T			downstream-variant-500B	RAB40B	GRCh38.p7	17:82656982	TCGTGCCATTGTACT[C/T]CACCCTGGGCAACAA	10966
rs760889224	snp	G/T	1.65132e-05	0.00287339	missense, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82664538	TCCAGCAGGATGGTG[G/T]TCGTCTTGTAGTCGA	10966
rs760958175	in-del	-/G			intron-variant	RAB40B	GRCh38.p7	17:82667445	GAGCACACCTGTGCA[-/G]CGCCTTCCATGAGAT	10966
rs760970327	in-del	-/T			intron-variant	RAB40B	GRCh38.p7	17:82685809	CTTCTTCTTCTTCTT[-/T]TTTTTTTTTTTTGAG	10966
rs760979079	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82688602	GCTGGGTGACAAAGC[A/G]AGACTCCGTCTCAAA	10966
rs761008455	in-del	-/TTC	1.65444e-05	0.00287609	cds-indel	RAB40B	GRCh38.p7	17:82657846	GAGATTCCGCCGTGT[-/TTC]TTTCAGTGCCTTCCT	10966
rs761021034	snp	A/G	1.65946e-05	0.00288046	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657814	GCTGCCGGGGGTAAC[A/G]CCGAGCTTCTCCTGG	10966
rs761064136	snp	A/G	3.29484e-05	0.00405871	synonymous-codon	RAB40B	GRCh38.p7	17:82657980	GGTGGTGAGGGAGTA[A/G]GAACCGCCGTGCATC	10966
rs761145294	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82678133	TTTTGTTTTTGTTTT[C/T]TACCTTATCTCCCAT	10966
rs761212011	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82677525	CCTTGCCACAGGTCC[A/G]AGGCCCAGAGGCGGC	10966
rs761299864	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665477	CAGGCTGGTCTCAAA[C/T]GCCTAAGTTCACACA	10966
rs761328950	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82682714	GAAATAGGCCCACAC[A/G]AAAATGGCCAATTGA	10966
rs761340406	snp	A/G	1.72549e-05	0.0029372	intron-variant	RAB40B	GRCh38.p7	17:82658159	GAAAAGATAAACCTT[A/G]CTTAGTGGATGTCCC	10966
rs761518347	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82675623	TAGATCAAGGTCCAG[A/G]CAGAGCCAGTGTCTG	10966
rs761611676	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82659848	AGCTCAGTGATAAAC[C/T]CTCAAATGTCACGGT	10966
rs761614642	snp	A/G	1.65736e-05	0.00287863	intron-variant	RAB40B	GRCh38.p7	17:82659539	CCTGACGTCCTCCCA[A/G]GCCTACAGGGATCTT	10966
rs761630201	snp	C/T	2.26242e-05	0.00336327	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657722	CGGGGTAGTGTGTTT[C/T]CATCACACGGAAGGC	10966
rs761633800	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82693287	GCTGGGATTGCAGAC[A/G]TGAGCCACCAGGCCC	10966
rs761656142	snp	C/T	1.73396e-05	0.0029444	missense	RAB40B	GRCh38.p7	17:82658701	CCAGGATCTTGGGGA[C/T]TCCGGGGGCATGCTA	10966
rs761720148	snp	A/G	5.01056e-05	0.00500503	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657777	TCGCCGAGAGGAACC[A/G]GGATCTGAGATGCAT	10966
rs761850500	snp	A/G	0.000733048	0.0191308	utr-variant-5-prime, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82698671	GCCCGGCCCCGAGAG[A/G]CGCCGCGCGGGCCCC	10966
rs761898236	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82664839	ACTGCAGGGCCTACA[C/T]GTGACCTGGAGGCCG	10966
rs761901094	snp	C/T	4.70666e-05	0.00485088	utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698612	CGTGACGGCCCGGCG[C/T]CCCCACCCATGCCCG	10966
rs761966529	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82658869	GACCGTCTTTGCAGA[C/T]GTAAATAGTTACGGT	10966
rs762040110	in-del	-/TA			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665453	GAGACGGGGTTTCGC[-/TA]TGTTTCCCAGGCTGG	10966
rs762084890	snp	C/G/T	3.29534e-05	0.00405904	missense	RAB40B	GRCh38.p7	17:82657967	TGTGGGTGGAGCTGG[C/G/T]GGTGAGGGAGTAGGA	10966
rs762098181	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82686569	AGCAGGGACTGGAAC[A/G]GTGCTGCCACAGGCC	10966
rs762110009	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82689942	ACTGCACTCCAGCCT[A/G]GGTGACAGAGCAAAA	10966
rs762145242	in-del	-/G/GG/GGGGGGGGTGG	0.00847402	0.0645395	frameshift-variant	RAB40B	GRCh38.p7	17:82657909	TTTTGGGGGGGCTCT[-/G/GG/GGGGGGGGTGG]GGGGGGGGCGGACGA	10966
rs762182570	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82691122	CGTGTAGTCTTGAGG[A/G]AGTGGCTCAGCCTCT	10966
rs762212974	in-del	-/CACACCAC	1.65127e-05	0.00287334	intron-variant	RAB40B	GRCh38.p7	17:82659669	ACCCTGGGGGAGAGG[-/CACACCAC]TCACAGGCTCAGCAC	10966
rs762222809	snp	C/T	1.65636e-05	0.00287776	missense, downstream-variant-500B	RAB40B	GRCh38.p7	17:82661009	CCCCGGGAGTAGGAG[C/T]GGAATATGGTACAAA	10966
rs762311117	snp	C/T	0.000117311	0.00765779	intron-variant	RAB40B	GRCh38.p7	17:82664455	AGCCAGGGGGGTTAC[C/T]CCCTGGGGGTGCGGG	10966
rs762385310	snp	A/G			utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657118	GAAACATTTTCCTAA[A/G]TAAGTGTTTTCACTT	10966
rs762432613	in-del	-/TTA			intron-variant	RAB40B	GRCh38.p7	17:82679258	AGGACACCACAAGCC[-/TTA]TTATTATTATTATTA	10966
rs762487686	in-del	-/CACA			intron-variant	RAB40B	GRCh38.p7	17:82682122	ACACACACACGCATG[-/CACA]CACACACACACACAG	10966
rs762576237	snp	A/G			intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660779	TGCACACACAGTCCC[A/G]TAAATGCACGCTTAC	10966
rs762667850	snp	A/G/T	5.11212e-05	0.00505554	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657714	AAGTCCGACGGGGTA[A/G/T]TGTGTTTCCATCACA	10966
rs762677767	snp	A/G					GRCh38.p7	17:82655670	GTTCTCACCCCACCT[A/G]TGGCACAGCAGAGAG	10966
rs762729019	snp	A/G			upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699143	CACCAGGGAGACCTC[A/G]GGTGCCTGGCCGGGT	10966
rs762735629	snp	C/G			intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661401	CTACACCAGGGGAGA[C/G]AGGCCGGTGGGATCC	10966
rs762748598	snp	G/T	0.000145291	0.00852199	utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698652	GCTGAGCGCAGAGGC[G/T]GCGGCCCGGCCCCGA	10966
rs762776218	snp	A/G	1.66599e-05	0.00288611	synonymous-codon	RAB40B	GRCh38.p7	17:82658609	CTCAAAGAAGGTCAC[A/G]CCCAGGCGCTCGGCG	10966
rs762803624	snp	A/G					GRCh38.p7	17:82655051	AGTCCGGTCTGTATT[A/G]GGTTTCGTCTGTTTT	10966
rs762831280	snp	C/G	3.70762e-05	0.00430543	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657643	AGAGTACTAATTTTC[C/G]CTTTACAAACACACA	10966
rs762834125	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82695340	GGGATTACAGGCACG[C/T]GGCACCACGCCCAGC	10966
rs762974804	snp	A/G	4.35047e-05	0.00466374	utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698603	GGCGCTCATCGTGAC[A/G]GCCCGGCGCCCCCAC	10966
rs762983532	in-del	-/TA	1.65712e-05	0.00287843	intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660982	TCGGGGGATGCTGTG[-/TA]TTACCTGTGCGCCCC	10966
rs763007057	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82683514	CAAAAGAGGCCAGAC[A/G]TAGTGGCTCACAACT	10966
rs763068312	in-del	-/AC			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671584	ACCCCTGTAACTCTA[-/AC]ACACACACTCACATG	10966
rs763069326	snp	A/T			stop-gained	RAB40B	GRCh38.p7	17:82657898	TTCTGGTGCAGTTTT[A/T]GGGGGGGCTCTGGGG	10966
rs763072920	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82687660	CTCCAGGACATGGCC[A/G]CCAGCTTCTGTGAGA	10966
rs763114457	in-del	-/A			intron-variant	RAB40B	GRCh38.p7	17:82684281	GAGTGGCTAACATTT[-/A]AAAAAAAACAAAACC	10966
rs763133851	in-del	-/TCTT			intron-variant	RAB40B	GRCh38.p7	17:82695180	GAACGCCCTCATCTT[-/TCTT]TCTTTCTTTCTTTCT	10966
rs763240403	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82670691	AGGCGCCCACCACCA[C/T]GCCCGGCTCATTTTT	10966
rs763243138	snp	A/G			intron-variant, downstream-variant-500B, missense	RAB40B, MIR4525	GRCh38.p7	17:82667909	CACGCTGAGTGCACC[A/G]TCTGTCTCTCTCTTC	10966
rs763442000	snp	C/T	5.0171e-05	0.00500829	synonymous-codon	RAB40B	GRCh38.p7	17:82658498	GGGCCTACCCTTGCT[C/T]GGCCGCCAGAGCCGG	10966
rs763454922	in-del	-/ACA			intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660694	CACACATGTACACAC[-/ACA]CACACACACAGGCAC	10966
rs763465796	snp	C/T			upstream-variant-2KB	RAB40B	GRCh38.p7	17:82700291	AGGCATGTGCCACCA[C/T]ACCCAGCTAATTTTT	10966
rs763509370	in-del	-/GTG			downstream-variant-500B	RAB40B	GRCh38.p7	17:82656875	AAAAATTAGCCGGGC[-/GTG]GTGGTGCACCTCTGT	10966
rs763552490	in-del	-/AA			intron-variant	RAB40B	GRCh38.p7	17:82683806	CAAGACCCTGTTTCC[-/AA]AAAAAAAAAAAAAAA	10966
rs763568945	snp	A/C/G	4.95768e-05	0.00497859	missense, synonymous-codon, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82664552	GGTCGTCTTGTAGTC[A/C/G]ATGCCTGCGGAAGGG	10966
rs763624168	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82686657	CCCGCTTAGAGCCTG[C/T]CAAGGGAGCGTGGCC	10966
rs763637226	snp	C/T	1.64732e-05	0.0028699	missense	RAB40B	GRCh38.p7	17:82657997	AACCGCCGTGCATCA[C/T]CCTGGCATTCAGGCC	10966
rs763717673	snp	C/G			upstream-variant-2KB	RAB40B	GRCh38.p7	17:82700577	TCCATGTTCCAATCA[C/G]CTGTGGGTCACATGG	10966
rs763752517	in-del	-/C			intron-variant	RAB40B	GRCh38.p7	17:82695209	TTCTTTTTTTTTTTT[-/C]CGAGACAAAATCTCA	10966
rs763766902	snp	C/T	4.99272e-05	0.00499611	intron-variant	RAB40B	GRCh38.p7	17:82664476	GGGGTGCGGGACGCT[C/T]GCACCTCCTCCAGAC	10966
rs763864160	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82693528	CTGTGCAGACATTTG[C/T]GTGCCTGATACCCAG	10966
rs763945727	snp	C/T	5.15256e-05	0.00507544	missense	RAB40B	GRCh38.p7	17:82658694	TTCCCCACCAGGATC[C/T]TGGGGACTCCGGGGG	10966
rs763962077	snp	A/T	0.000155872	0.00882677	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657645	AGTACTAATTTTCCC[A/T]TTACAAACACACATC	10966
rs763968492	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82693151	GGGAATACAGGTGCC[C/T]GCCACCACACCTGGC	10966
rs764022512	snp	A/G	2.20656e-05	0.00332149	utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698604	GCGCTCATCGTGACG[A/G]CCCGGCGCCCCCACC	10966
rs764066799	snp	G/T	1.76902e-05	0.00297402	missense, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698532	TTGCCCACGTCGCTG[G/T]CGCCCACCAGCAGGA	10966
rs764146112	snp	C/T	1.66679e-05	0.00288681	missense	RAB40B	GRCh38.p7	17:82658611	CAAAGAAGGTCACGC[C/T]CAGGCGCTCGGCGTA	10966
rs764231638	snp	A/T			intron-variant	RAB40B	GRCh38.p7	17:82695944	TACAATGGTGCGATC[A/T]CTGCAACCTCCGCCT	10966
rs764233331	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82670871	CTACGAGTTTCAAAA[C/T]CATCTTTCGTTTCTG	10966
rs764243082	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82673594	CATACAATTGAGGGA[A/G]AAGATGCTTTTCCCT	10966
rs764504862	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665388	CCCCTGAGTAGCCGG[A/G]ACTACGGGCATGTGC	10966
rs764520009	in-del	-/G			frameshift-variant	RAB40B	GRCh38.p7	17:82657898	TCTGGTGCAGTTTTT[-/G]GGGGGGGCTCTGGGG	10966
rs764583570	snp	C/G/T	5.21076e-05	0.00510407	synonymous-codon	RAB40B	GRCh38.p7	17:82657899	TCTGGTGCAGTTTTT[C/G/T]GGGGGGCTCTGGGGG	10966
rs764678758	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666706	AGAGGGTTTGAGTTA[A/G]GGGGCTGGAGAATGC	10966
rs764792723	snp	G/T	1.66051e-05	0.00288137	missense, downstream-variant-500B	RAB40B	GRCh38.p7	17:82661034	TACAAAATCTTCCCT[G/T]GCCTGAAGTATCCCT	10966
rs764807338	in-del	-/T			intron-variant	RAB40B	GRCh38.p7	17:82678879	AGCTCCCTTTCTGCG[-/T]TTTTTTTTTTTTTTT	10966
rs764881539	snp	C/G			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669768	CGCTTTGAGCGACGA[C/G]CAAAAATCTCTTCAC	10966
rs764883782	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82659244	GGCTGGTCTGCGTGC[C/T]AGCAGGCACAAGCGC	10966
rs764908893	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82691854	ACCCCTGCCTGGAGA[C/G]AAATGGAACTTCCGA	10966
rs764917189	snp	A/G	1.65872e-05	0.00287981	synonymous-codon	RAB40B	GRCh38.p7	17:82658530	CCATCCCATGCCGCA[A/G]CAGCACGATCCTGGC	10966
rs764972468	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82659924	AGGATGCAGGGGCAC[C/T]GCAGTAATCGCCACC	10966
rs764987772	snp	C/T			intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660611	ATACACTGCACATAC[C/T]TGCACACACGTGCAC	10966
rs765137929	snp	C/T					GRCh38.p7	17:82654933	ATCTAAAGCAACAGG[C/T]CACACCTCTGAACAT	10966
rs765157089	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82681974	AGAAAATATTTTCCC[C/T]ATGAAAATATCCACT	10966
rs765205531	in-del	-/T			intron-variant	RAB40B	GRCh38.p7	17:82686106	CGCACCCAGCCTTCT[-/T]TTTTTTTTTTTTTTT	10966
rs765210724	snp	A/G	1.69631e-05	0.00291226	intron-variant	RAB40B	GRCh38.p7	17:82698447	GCACGCCCTCCGCCC[A/G]CGCTCACCCGCCGGG	10966
rs765268430	snp	C/T	1.65269e-05	0.00287457	synonymous-codon	RAB40B	GRCh38.p7	17:82657884	AATTTTGCAGCTGTT[C/T]CTGGTGCAGTTTTTG	10966
rs765373270	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82675119	ACTGGGAAAAGCTAC[A/G]AAGGATGCATTTTCA	10966
rs765386184	in-del	-/TCAAAAAAAA			intron-variant	RAB40B	GRCh38.p7	17:82681019	GAGCAAGACTCCATC[-/TCAAAAAAAA]AAAAAAAAAAAAAAA	10966
rs765395569	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82662971	GGAAGGAGTGGTCTC[C/G]GGGAGGGAGGGAGAG	10966
rs765457781	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82686638	AGGGGAGTCAGGAAG[A/G]GTCCCCGCTTAGAGC	10966
rs765475581	snp	C/G	1.66076e-05	0.00288158	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657807	TCCACCAGCTGCCGG[C/G]GGTAACGCCGAGCTT	10966
rs765550489	in-del	-/AGG			intron-variant	RAB40B	GRCh38.p7	17:82691476	GGATTGCCTGAGGTC[-/AGG]AGTTCGAGACCAGCC	10966
rs765617141	in-del	-/GCACCTGCCACCA	1.65127e-05	0.00287334	intron-variant	RAB40B	GRCh38.p7	17:82659670	CCCTGGGGGAGAGGT[-/GCACCTGCCACCA]CACAGGCTCAGCACG	10966
rs765630877	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666999	GCTGAGAGGCCGAGG[A/G]GAGAAGCAGCGCCGA	10966
rs765650659	snp	A/G			downstream-variant-500B	RAB40B	GRCh38.p7	17:82657059	TCGAAAGAACCGGTC[A/G]CCAACTCTACCAAGA	10966
rs765707229	in-del	-/CA			intron-variant	RAB40B	GRCh38.p7	17:82660041	GTGCACAGATGCACG[-/CA]CACACAGTGCACGTA	10966
rs765769136	snp	G/T			intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660792	CCGTAAATGCACGCT[G/T]ACATCCGTAATACTG	10966
rs765825417	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82697672	CTCTGCGCGTTCCCC[C/G]TTCTCCTGGGTTCCT	10966
rs765865161	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82688808	GCATGGTGGTGCATG[C/T]CTGTAATCCCAGCTA	10966
rs765884225	snp	A/G			upstream-variant-2KB	RAB40B	GRCh38.p7	17:82700041	AGTCAAGATTATTAT[A/G]TTTGTCATTTGCATT	10966
rs765950087	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82677572	CATCAGCCCTGACGC[C/T]GCGTCTCTGTCCCTG	10966
rs766078075	snp	C/T	4.33116e-05	0.00465338	intron-variant	RAB40B	GRCh38.p7	17:82698409	AGCCCCGCGCCCCTC[C/T]CCGGCCCCGCGCCCG	10966
rs766126527	in-del	-/AC			intron-variant	RAB40B	GRCh38.p7	17:82667691	AGATTAGACCAAGCA[-/AC]ACCAGAGCAAACTCC	10966
rs766157988	snp	A/G					GRCh38.p7	17:82655709	ACAGGTCTTTGCAGC[A/G]TGCCTGCACGAGGCT	10966
rs766184510	in-del	-/C			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671187	GTACTCACTGACACA[-/C]CCCACCCCCGTAACT	10966
rs766206437	snp	C/T			utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657210	AACTAGAGGTATCTT[C/T]GGCATTTTCTTCCCT	10966
rs766296794	in-del	-/A	1.64749e-05	0.00287005	frameshift-variant	RAB40B	GRCh38.p7	17:82657939	AGCTTCACTTTGCGG[-/A]GGCTGCTCCTTTTGT	10966
rs766299807	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82675775	ATCTTCCAATAGCCC[C/T]ATCTTCTAACACCAT	10966
rs766304170	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82683531	AGTGGCTCACAACTG[C/T]AATCCCACCACTTTG	10966
rs766335979	in-del	-/A			intron-variant	RAB40B	GRCh38.p7	17:82683357	TATTCTTTAAAAGAT[-/A]ACTAAATGGAAAGAA	10966
rs766337439	snp	A/G	3.82124e-05	0.0043709	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657734	TTTCCATCACACGGA[A/G]GGCGTCGCACACATT	10966
rs766424870	snp	A/G	1.65269e-05	0.00287457	intron-variant	RAB40B	GRCh38.p7	17:82659565	ATCTTGGGCAGTGGC[A/G]TTTCTACAACATACC	10966
rs766432329	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82660012	ACATGGAGCTCACGC[A/G]CACACAGGCACTTGT	10966
rs766432994	in-del	-/AC			intron-variant	RAB40B	GRCh38.p7	17:82660354	TGCACGCACGTGTAC[-/AC]ACACACACACGCACA	10966
rs766461100	in-del	-/C	1.81587e-05	0.00301314	intron-variant, utr-variant-5-prime, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661089	AAGAAACCAGTGCTT[-/C]CTTCCTGACAACAGG	10966
rs766468264	snp	G/T			intron-variant	RAB40B	GRCh38.p7	17:82684613	GCAATGAGCTCTTGG[G/T]GCACCTGACAAGTCA	10966
rs766523851	snp	A/G					GRCh38.p7	17:82655079	TTTTGTTCTGCCTTG[A/G]TTTGCTGTAGCACTT	10966
rs766538636	snp	C/T	1.66244e-05	0.00288304	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657804	GCATCCACCAGCTGC[C/T]GGGGGTAACGCCGAG	10966
rs766608808	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82663182	TGCAGCAGGAAGGGT[C/T]GGGGCGCTTGGGGAC	10966
rs766608973	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82676118	GAATGGGGAACCGAC[C/T]GCCTCGTGGGACGCA	10966
rs766634933	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82682436	AATAAATGGAGAGAC[A/G]TACCATGTTCATGAT	10966
rs766722986	snp	A/C			intron-variant	RAB40B	GRCh38.p7	17:82697862	CCCCTCTTCCGCACG[A/C]GAGTCACCTGTGCTC	10966
rs766732740	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82686661	CTTAGAGCCTGCCAA[A/G]GGAGCGTGGCCCAGG	10966
rs766736972	in-del	-/ACAG			intron-variant	RAB40B	GRCh38.p7	17:82660098	CGCAGGCACTCATGC[-/ACAG]ACACAGTGCACATAC	10966
rs766856610	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82659105	GGGCTCTGGCCTCCA[C/G]AACCGTGAGAGAATG	10966
rs766935458	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82687680	CTTCTGTGAGAGGTG[C/T]TGGCATCCTCGGAGA	10966
rs766988921	snp	A/T			intron-variant	RAB40B	GRCh38.p7	17:82678324	TCTGTCCATCAAAAT[A/T]TAATAAAGATATACA	10966
rs766995882	snp	A/T	1.73498e-05	0.00294527	intron-variant	RAB40B	GRCh38.p7	17:82658161	AAAGATAAACCTTGC[A/T]TAGTGGATGTCCCCA	10966
rs767016544	snp	C/T	1.64741e-05	0.00286998	missense	RAB40B	GRCh38.p7	17:82657985	TGAGGGAGTAGGAAC[C/T]GCCGTGCATCATCCT	10966
rs767018687	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82675213	ACTGGAAATAAAATC[A/G]AACTCAGTGATAATG	10966
rs767087358	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82691677	ACAGAGCGAGACTCC[A/G]TCTCAAAAAACAACA	10966
rs767156411	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82693296	GCAGACGTGAGCCAC[C/T]AGGCCCGGCCGACTT	10966
rs767175482	snp	A/C	1.64882e-05	0.00287121	missense	RAB40B	GRCh38.p7	17:82658093	GGTGCACCGGCGTGC[A/C]GGACACGACCGCCCG	10966
rs767191577	snp	A/G	1.66599e-05	0.00288611	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657787	GAACCGGGATCTGAG[A/G]TGCATCCACCAGCTG	10966
rs767219695	snp	A/G			intron-variant, downstream-variant-500B, utr-variant-5-prime	RAB40B, MIR4525	GRCh38.p7	17:82667936	CTTCTTGGCATGGGC[A/G]CTGACGGGGCACTGA	10966
rs767269113	in-del	-/AT			intron-variant	RAB40B	GRCh38.p7	17:82660176	TGCATACCTGCACAC[-/AT]GTTGCATACACATAC	10966
rs767374066	in-del	-/A	1.65616e-05	0.00287759	intron-variant	RAB40B	GRCh38.p7	17:82664572	CTGCGGAAGGGTTAG[-/A]GACGGCTTAGGCCTG	10966
rs767433307	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82673089	GGCGCCTGTAGTCCC[A/G]GATACTTGGGAGGCT	10966
rs767485614	snp	C/G	1.66854e-05	0.00288833	missense	RAB40B	GRCh38.p7	17:82658618	GGTCACGCCCAGGCG[C/G]TCGGCGTAGGCCTGG	10966
rs767591042	snp	A/T	2.10866e-05	0.00324698	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657727	TAGTGTGTTTCCATC[A/T]CACGGAAGGCGTCGC	10966
rs767606237	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671936	ACATGCTCCCTGTAC[C/T]CACTGACACAGCTCA	10966
rs767624414	snp	C/T	0.000831255	0.02037	upstream-variant-2KB	RAB40B	GRCh38.p7	17:82698734	GCCCAGCGCTGACAG[C/T]GCGCATCCCCGCCCG	10966
rs767624554	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82695689	GCACTCCAGCCTGGG[C/T]GGCAGAGAAGACCCT	10966
rs767729396	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82686030	GCTGGTCTCAAACTG[C/T]TGAACTCGTGATCTG	10966
rs767730858	snp	A/G	1.65507e-05	0.00287664	intron-variant	RAB40B	GRCh38.p7	17:82659685	TCACAGGCTCAGCAC[A/G]CAGAACACAGATGCA	10966
rs767742075	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665462	TTTCGCTATGTTTCC[C/T]AGGCTGGTCTCAAAC	10966
rs767754003	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82683824	AAAAAAAAAAAAAAA[C/G]AAAAGAAAAGAAAAG	10966
rs767836607	snp	C/G					GRCh38.p7	17:82655730	GCACGAGGCTGGCCA[C/G]CCTCTCCAGACACTG	10966
rs767841700	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82676256	ACCCCTCACCTTCAA[C/T]AGCATCTCCCCCACA	10966
rs767853079	snp	A/G			downstream-variant-500B	RAB40B	GRCh38.p7	17:82656929	TGAGGCAGGAGAATC[A/G]CTTGAACCCGGGAGG	10966
rs767901689	in-del	-/TTT					GRCh38.p7	17:82655952	TCCCTTAAATTTCTT[-/TTT]TTTTTTTTTTTTTTT	10966
rs767973913	snp	A/G	3.29766e-05	0.00406045	synonymous-codon	RAB40B	GRCh38.p7	17:82657914	GGGGGGGCTCTGGGG[A/G]GGGCGGACGAGCTTC	10966
rs768082115	snp	A/T	1.66241e-05	0.00288302	intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660944	TGTAAATGTTATTAT[A/T]CAAAGTTGGTTTGAT	10966
rs768090752	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82677437	AAAGCATTACAAGCC[A/G]GGCTGCTTCCAGGAG	10966
rs768108320	snp	C/G					GRCh38.p7	17:82654750	GAGACGGGGTTTCAT[C/G]ATGTTGCCCAGGCTG	10966
rs768126214	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82695221	TTTTCGAGACAAAAT[C/G]TCACTCTGTCGCTGG	10966
rs768143592	snp	G/T			intron-variant	RAB40B	GRCh38.p7	17:82673751	TGGGCCTTGCTGTAG[G/T]GATCTTCGTGGCCAG	10966
rs768163202	in-del	-/A			intron-variant	RAB40B	GRCh38.p7	17:82689812	CTCCACTAAAACTAC[-/A]AAAAAATTAGCTGGA	10966
rs768174080	snp	A/G	4.96874e-05	0.0049841	missense, downstream-variant-500B	RAB40B	GRCh38.p7	17:82661010	CCCGGGAGTAGGAGC[A/G]GAATATGGTACAAAA	10966
rs768235894	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82694257	AATTCAGGCCGCGCA[C/T]TGTGGCTCACACCTG	10966
rs768245374	snp	C/T	3.31395e-05	0.00407046	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657826	AACGCCGAGCTTCTC[C/T]TGGAGAGATTCCGCC	10966
rs768269536	snp	C/T					GRCh38.p7	17:82655378	CAAAGAGCTCTGAGT[C/T]ACAAAGCCTTGGGAA	10966
rs768375281	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82688258	ACTCCTGAGCTCAAG[C/T]GATCCCAAAGTGCTG	10966
rs768377228	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82687345	TTAGGGTCACTAAAG[C/T]TTAATATGTATATTT	10966
rs768438000	snp	A/G	1.64974e-05	0.00287201	synonymous-codon	RAB40B	GRCh38.p7	17:82659637	CCAGCGGTTCGCAAT[A/G]TCATAGACCAGGATC	10966
rs768465585	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82675901	GCCCTCCATCTGCTA[C/T]GTGGGTCCTTCTCAC	10966
rs768497802	snp	A/C/G	0.000866176	0.0207927	utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698659	GCAGAGGCGGCGGCC[A/C/G]GGCCCCGAGAGGCGC	10966
rs768581948	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82667719	CTCCCCCCGTCAGAG[A/G]AGAGTGATTCAGAGG	10966
rs768662139	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82685789	CTGATTCGGAAACAG[A/G]ATCTCTTCTTCTTCT	10966
rs768685287	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82681613	CCAATCATTAAAATA[A/G]CTTACTATACAATAA	10966
rs768754845	snp	A/C/G	3.29507e-05	0.00405887	missense	RAB40B	GRCh38.p7	17:82657960	CTCCTTTTGTGGGTG[A/C/G]AGCTGGTGGTGAGGG	10966
rs768769731	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82689836	AGCTGGACGTGATGG[C/T]GGGCACCTGTAATCC	10966
rs768804451	in-del	-/C			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671626	CACTGACACAGCTCA[-/C]CCCGTAACTCTAACA	10966
rs768818008	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669319	TGTCTCTGCTAAAAA[C/T]ACGAAATTAGCCGGG	10966
rs768900432	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668545	AACAGCGCCCAGTCC[C/T]GAGGGGGCTGAGGTG	10966
rs768947268	snp	G/T	1.68001e-05	0.00289823	intron-variant	RAB40B	GRCh38.p7	17:82664445	GTGCTATGCCAGCCA[G/T]GGGGGTTACTCCCTG	10966
rs769047078	snp	A/G	9.52381e-05	0.0069	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657698	TCCACGTAGAAATTC[A/G]AAGTCCGACGGGGTA	10966
rs769057308	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82689852	GGGCACCTGTAATCC[A/G]AGCTACTCAGGAGGC	10966
rs769093356	snp	A/G			intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661345	GGCTTTAAAAAACTT[A/G]TTGAATCTGAAGATA	10966
rs769165434	snp	A/C			intron-variant	RAB40B	GRCh38.p7	17:82680386	GCTCGGGGGACGGGA[A/C]GGCAGTTCCCCCACG	10966
rs769215576	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82696972	GACCTGCCACCGAGC[A/G]GGGAGGGGGGTAGGA	10966
rs769232492	in-del	-/C	1.65537e-05	0.0028769	intron-variant	RAB40B	GRCh38.p7	17:82659552	CAAGCCTACAGGGAT[-/C]TTGGGCAGTGGCATT	10966
rs769298609	snp	C/G					GRCh38.p7	17:82656418	GGTCTTTGCGGTCAG[C/G]CCTGCTCTGAGGCAG	10966
rs769333212	snp	A/T			intron-variant	RAB40B	GRCh38.p7	17:82680674	TAGTAGTAATACCTA[A/T]AATGATATATGTAAT	10966
rs769355408	snp	C/T					GRCh38.p7	17:82656188	TCCTGACCTCTGATC[C/T]GGCTGCCTCGGCCTC	10966
rs769385803	snp	C/T	2.16251e-05	0.00328818	intron-variant	RAB40B	GRCh38.p7	17:82658760	GTTACTTCAGTGAGA[C/T]TTTGTTGTCGTCGTA	10966
rs769387097	in-del	-/TG			intron-variant	RAB40B	GRCh38.p7	17:82682120	ACACACACACACGCA[-/TG]CACACACACACACAC	10966
rs769388257	in-del	-/A	0.000119424	0.00772644	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657662	TACAAACACACATCG[-/A]AAACAAGAGCTTCAT	10966
rs769388496	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82683436	ACTTACATCCAAAAC[A/G]TATTTAAACATTCTC	10966
rs769388917	snp	A/G	5.18506e-05	0.00509143	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657751	GCGTCGCACACATTC[A/G]CAAGCAGCATTCGCC	10966
rs769557642	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82670445	CTGCCTTGGCCTCCC[A/G]AAGTGCTAGGATTAT	10966
rs769578411	snp	G/T			intron-variant	RAB40B	GRCh38.p7	17:82672879	TTATTTTTCCTTCAT[G/T]TACGAATTTTTGTTT	10966
rs769582459	snp	C/T	1.68593e-05	0.00290334	synonymous-codon	RAB40B	GRCh38.p7	17:82658663	CACCTGCCGCTTGAA[C/T]GCCAGGTGCAGGCGG	10966
rs769597064	in-del	-/AG			intron-variant	RAB40B	GRCh38.p7	17:82687256	AATTTTATTAATCTA[-/AG]AGAAAATTTCATACT	10966
rs769641556	in-del	-/ACCTGTGCAG			intron-variant	RAB40B	GRCh38.p7	17:82667436	GCCTGATCTGAGCAC[-/ACCTGTGCAG]CGCCTTCCATGAGAT	10966
rs769658789	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668794	CAGGGCAGCGGGCCG[C/T]GGCACGCAGGGAAGG	10966
rs769688767	snp	C/T	2.09677e-05	0.00323781	utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698597	GCCCAGGGCGCTCAT[C/T]GTGACGGCCCGGCGC	10966
rs769773881	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666393	GGAATTACAGGCATA[C/T]ACCGCCACGTCCAGC	10966
rs769789553	snp	A/G					GRCh38.p7	17:82655592	GTGGGTTTCTTCAAC[A/G]TGGACTCTCCTTTCT	10966
rs769817805	snp	A/C			intron-variant	RAB40B	GRCh38.p7	17:82659059	GGGAGAGGCGGCTGT[A/C]GGGAAGTGGCCCTGC	10966
rs769838413	snp	C/T					GRCh38.p7	17:82655980	TTTTAGATGGAGTTT[C/T]ACTTGTCGCCCAGGC	10966
rs769882409	snp	C/G	1.65641e-05	0.00287781	missense, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660989	GATGCTGTGTTACCT[C/G]TGCGCCCCGGGAGTA	10966
rs769996766	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82673153	AGGTTGCAGTGAGCT[A/G]AGATCGTGCAACTGC	10966
rs770072517	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82676052	GATCAAATCCAGTCC[C/T]AACACCAATGTCTTC	10966
rs770187096	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82694079	CAGAGCGAGACTCCA[C/T]CTCAAAAAAAAAAAA	10966
rs770188069	snp	A/C			intron-variant	RAB40B	GRCh38.p7	17:82680512	TAAAAAAAATATCGC[A/C]TATGAAAAAGCTTAT	10966
rs770213067	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82682181	CCTCTCCAAAAACCA[A/G]TAAGAAAGCTATTAG	10966
rs770216642	snp	G/T			intron-variant, utr-variant-5-prime, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661219	TGAAGGGATCCGGGT[G/T]TTGGGATGTCCTCCC	10966
rs770238101	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82692687	ATGTCAAAGGTAAAA[C/G]GATGCTTGTAGAGAA	10966
rs770317218	snp	A/G	9.95504e-05	0.00705445	synonymous-codon	RAB40B	GRCh38.p7	17:82658588	GAAATTGCACAGAGG[A/G]CTGACCTCAAAGAAG	10966
rs770344413	snp	A/G	1.70472e-05	0.00291947	intron-variant	RAB40B	GRCh38.p7	17:82658150	CTTGGGAGAGAAAAG[A/G]TAAACCTTGCTTAGT	10966
rs770442137	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82683090	GGAGCTTGCAGTGAG[C/T]CGAGATCATGCCACT	10966
rs770442329	snp	C/T	5.2561e-05	0.00512618	utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698639	CCCGGCCTGCGGGGC[C/T]GAGCGCAGAGGCGGC	10966
rs770463962	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82686269	GGCACCTGCCACCAC[A/G]CCCAGCTAATTTTTG	10966
rs770469119	in-del	-/T	1.65736e-05	0.00287863	intron-variant	RAB40B	GRCh38.p7	17:82659539	CTGACGTCCTCCCAA[-/T]GCCTACAGGGATCTT	10966
rs770513487	snp	C/T	1.98081e-05	0.003147	missense, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698593	GGCTGCCCAGGGCGC[C/T]CATCGTGACGGCCCG	10966
rs770515485	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82691144	TCAGCCTCTCTGGGC[C/T]TCACAATATAACCTC	10966
rs770678910	snp	A/C	1.64751e-05	0.00287007	missense	RAB40B	GRCh38.p7	17:82657926	GGGGGGGCGGACGAG[A/C]TTCACTTTGCGGAGG	10966
rs770718454	snp	A/G	1.67475e-05	0.00289369	stop-gained	RAB40B	GRCh38.p7	17:82657910	TTTTGGGGGGGCTCT[A/G]GGGGGGGCGGACGAG	10966
rs770729549	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82659460	TGCTGGAGCGCCATC[C/T]GGTGCCCTGGCCTGT	10966
rs770750585	snp	A/C			downstream-variant-500B	RAB40B	GRCh38.p7	17:82656764	CACGCCTGTAATCCC[A/C]GCACTTTGGGAGGCC	10966
rs770753183	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82681392	GGGAGAAGTCTCCTA[A/G]TACAGGAAGCAGTAG	10966
rs770787173	snp	A/C	3.30743e-05	0.00406645	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657853	CGCCGTGTTTCTTTC[A/C]GTGCCTTCCTTAAGA	10966
rs770808978	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666511	CGGCCTCCCAAAGTG[C/T]TGGGATTACAGGCAT	10966
rs770854308	in-del	-/AC			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671472	ACCCCTGTAACTCTA[-/AC]ACACACACTCACATG	10966
rs770944401	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82660227	GATGCACACACAGTG[C/T]ACACACGCAGTTCAT	10966
rs771064735	snp	A/G	3.30349e-05	0.00406403	intron-variant	RAB40B	GRCh38.p7	17:82659674	TGGGGGAGAGGTCAC[A/G]GGCTCAGCACGCAGA	10966
rs771143411	snp	A/G	3.32734e-05	0.00407868	synonymous-codon, downstream-variant-500B	RAB40B	GRCh38.p7	17:82661041	TCTTCCCTGGCCTGA[A/G]GTATCCCTGGAAAAG	10966
rs771167707	snp	A/G	1.66222e-05	0.00288285	intron-variant	RAB40B	GRCh38.p7	17:82664593	CTTAGGCCTGAGGCT[A/G]CAGCTAACAGGACGC	10966
rs771186342	snp	A/T	1.68872e-05	0.00290574	intron-variant	RAB40B	GRCh38.p7	17:82658476	GGTGGCCCCCGGAAT[A/T]GCCCCTGGGCCTACC	10966
rs771206046	in-del	-/ATCT			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669565	GGCTGAGGTGGAAGG[-/ATCT]CTTGAACCCGGGAGT	10966
rs771269900	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82679367	GCTCACTGCAAGCTC[C/T]GCCTCCTGGGTTCAC	10966
rs771270963	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82677238	AGGCGTGAGCCACCG[C/T]TCCCGGCCAGCCTAC	10966
rs771364168	snp	A/C			intron-variant	RAB40B	GRCh38.p7	17:82682384	CTTATATATTAAAAG[A/C]TACAAACCACTAATA	10966
rs771461059	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82696967	CTAGAGACCTGCCAC[C/G]GAGCGGGGAGGGGGG	10966
rs771479021	snp	A/G	1.69198e-05	0.00290854	intron-variant	RAB40B	GRCh38.p7	17:82658144	TCAGCACTTGGGAGA[A/G]AAAAGATAAACCTTG	10966
rs771489045	snp	A/T	1.65135e-05	0.00287341	missense, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82664539	CCAGCAGGATGGTGG[A/T]CGTCTTGTAGTCGAT	10966
rs771599033	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82663784	TCAACCACGCTGCAT[C/T]GGTCCCCTCTTGGCA	10966
rs771629290	snp	G/T	1.65416e-05	0.00287586	missense	RAB40B	GRCh38.p7	17:82657907	AGTTTTTGGGGGGGC[G/T]CTGGGGGGGGCGGAC	10966
rs771641599	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82681744	TTTGAAAATCTATCA[A/G]TGCAATTTATCACAT	10966
rs771683284	snp	A/G			missense, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698574	AAGTCGTAGGCCCGG[A/G]CCGGGCTGCCCAGGG	10966
rs771787098	snp	A/T			upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699589	TGCAGGTGTCTGCAC[A/T]TGTATGTGCGTGTGC	10966
rs771869315	snp	A/G	1.65021e-05	0.00287241	missense	RAB40B	GRCh38.p7	17:82659653	TCATAGACCAGGATC[A/G]CACCCTGGGGGAGAG	10966
rs771902268	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82694020	CCTGGGAGGCAGAGG[C/T]TGCAGTGAGCTGAGA	10966
rs772083106	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82678035	TTTCATAGCTATGTT[C/G]AAATTCAATTTGTGA	10966
rs772239461	snp	C/T	1.66081e-05	0.00288163	synonymous-codon	RAB40B	GRCh38.p7	17:82658124	GCAGCAGAGGTCTTG[C/T]AAGCTCAGCACTTGG	10966
rs772306573	in-del	-/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671517	GACACACCCCACCCC[-/T]TGTAACTCTAACACA	10966
rs772341150	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82667616	GCTTCCCGCATCCTC[C/T]TCTGTCTCCTGCTAA	10966
rs772380615	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82697278	TCCCTTGGTGCTCAC[A/G]CCGCCTGCCTGGAGC	10966
rs772403279	in-del	-/TT			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82670536	AAAAGAATTCCTGAT[-/TT]TTTTTTTTTTTTTTT	10966
rs772468950	in-del	-/T	3.31711e-05	0.0040724	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657843	GGAGAGATTCCGCCG[-/T]GTTTCTTTCAGTGCC	10966
rs772526436	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82670324	CGTGTAGCTGGAATT[A/G]CAGGCACACGCCAGC	10966
rs772542817	snp	G/T	3.34728e-05	0.00409088	intron-variant	RAB40B	GRCh38.p7	17:82664464	GGTTACTCCCTGGGG[G/T]TGCGGGACGCTCGCA	10966
rs772577082	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82683484	AAATAAACAATTCAG[C/G]TTTTTCAAAATAAGC	10966
rs772582291	snp	A/T	3.40942e-05	0.00412867	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657706	GAAATTCGAAGTCCG[A/T]CGGGGTAGTGTGTTT	10966
rs772608239	snp	C/T					GRCh38.p7	17:82656508	CGAGGCTCAGGAGCA[C/T]GGCTCTGATTTCTCA	10966
rs772612675	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82660373	CACACACGCACAGGC[A/G]CTCATGCACAGATGC	10966
rs772668794	snp	C/G			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82670455	CTCCCAAAGTGCTAG[C/G]ATTATAGGCATGAGC	10966
rs772866248	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82672947	GATGGTTCATGCCTG[C/T]AATCCCAGCACTTTG	10966
rs772979637	snp	C/T	2.00535e-05	0.00316644	missense, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698479	GGCCGTACGGGGACT[C/T]GGCCGCGCCATCCTG	10966
rs773054511	snp	G/T					GRCh38.p7	17:82656448	GTCGGGGTCAGGGGC[G/T]ACATCTTCATGCGGA	10966
rs773074955	snp	A/G	1.65091e-05	0.00287303	intron-variant	RAB40B	GRCh38.p7	17:82659664	GATCACACCCTGGGG[A/G]AGAGGTCACAGGCTC	10966
rs773136679	snp	C/G					GRCh38.p7	17:82655665	CTGTCGTTCTCACCC[C/G]ACCTGTGGCACAGCA	10966
rs773163299	snp	A/G	1.65652e-05	0.0028779	intron-variant	RAB40B	GRCh38.p7	17:82659547	CCTCCCAAGCCTACA[A/G]GGATCTTGGGCAGTG	10966
rs773163351	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82682760	CAAAGGCCATACAAT[A/G]AAGAATAGTCTTTTC	10966
rs773243922	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82659074	AGGGAAGTGGCCCTG[C/T]CGACACCTTGGTTTT	10966
rs773271819	snp	G/T					GRCh38.p7	17:82654707	GACGTGCACCACCAT[G/T]CCCGGCTAGTGGTTT	10966
rs773336240	snp	A/C	4.96931e-05	0.00498439	intron-variant	RAB40B	GRCh38.p7	17:82659546	TCCTCCCAAGCCTAC[A/C]GGGATCTTGGGCAGT	10966
rs773432813	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82687611	TGTTACAATGGCCTC[A/G]TTGTTCTCCACTGAC	10966
rs773449901	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82681724	AATGCAAGGTTGGTT[C/T]GACCTTTGAAAATCT	10966
rs773482878	in-del	-/CAG	1.65296e-05	0.00287481	intron-variant	RAB40B	GRCh38.p7	17:82659678	GAGAGGTCACAGGCT[-/CAG]CAGCACGCAGAACAC	10966
rs773518741	snp	A/G	1.64779e-05	0.00287031	missense	RAB40B	GRCh38.p7	17:82658066	CAATGGGGAGCGGGA[A/G]CTTGTCCACCAGGTG	10966
rs773522891	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82688195	CCCAGCTAATTTTTA[A/G]ACTTTCTGTAGAGAC	10966
rs773525501	snp	C/T	0.000197342	0.00993138	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657707	AAATTCGAAGTCCGA[C/T]GGGGTAGTGTGTTTC	10966
rs773629565	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82691408	CATGTGCAAAAGGCC[A/G]GGCGCGGTGGCTCAC	10966
rs773712199	in-del	-/AAAA			intron-variant	RAB40B	GRCh38.p7	17:82683807	AGACCCTGTTTCCAA[-/AAAA]AAAAAAAAAAAAAAA	10966
rs773717114	snp	A/G	1.65124e-05	0.00287331	missense, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82664532	CGCCCGTCCAGCAGG[A/G]TGGTGGTCGTCTTGT	10966
rs773797370	snp	C/T			intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661531	AGGCAGGGCTTGAGT[C/T]CTCAGATGACGGCAC	10966
rs773837693	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82692846	GGAGTGGAAAGGTGA[C/T]GTGCAGATGAGAGTG	10966
rs773914957	snp	C/T	1.67536e-05	0.00289423	intron-variant	RAB40B	GRCh38.p7	17:82664467	TACTCCCTGGGGGTG[C/T]GGGACGCTCGCACCT	10966
rs773920723	in-del	-/A/AA			intron-variant	RAB40B	GRCh38.p7	17:82689965	AGCAAAACTTCATCT[-/A/AA]CAAAAAAAAAAAAAA	10966
rs773973983	in-del	-/TC			intron-variant	RAB40B	GRCh38.p7	17:82695188	TCATCTTTCTTTCTT[-/TC]TTTCTTTCTTTTTTT	10966
rs773996786	snp	A/G			intron-variant, synonymous-codon	RAB40B	GRCh38.p7	17:82662683	CAGGAGAGCAGCCTC[A/G]GGGTCCTGCTGGGGC	10966
rs774025878	snp	A/G	1.65751e-05	0.00287876	intron-variant	RAB40B	GRCh38.p7	17:82659538	GCCTGACGTCCTCCC[A/G]AGCCTACAGGGATCT	10966
rs774102898	snp	C/T	1.67178e-05	0.00289113	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657776	TTCGCCGAGAGGAAC[C/T]GGGATCTGAGATGCA	10966
rs774190466	snp	G/T	3.31362e-05	0.00407026	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657827	ACGCCGAGCTTCTCC[G/T]GGAGAGATTCCGCCG	10966
rs774193991	snp	A/C/T			intron-variant	RAB40B	GRCh38.p7	17:82697260	CCTCCAGCCGTGCCA[A/C/T]ACTCCCTTGGTGCTC	10966
rs774297387	snp	C/T	2.43241e-05	0.00348733	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657717	TCCGACGGGGTAGTG[C/T]GTTTCCATCACACGG	10966
rs774421421	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82687314	CTATTAAGATAATAA[C/G]TTCTGGCCTTATGTA	10966
rs774422547	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82685957	TACAGGTGCCCGCCA[C/T]CACACCCAGCTAATT	10966
rs774461941	snp	A/G					GRCh38.p7	17:82656394	ACCAGGGAAGAGAGC[A/G]GCCCTGGAGGTCTTT	10966
rs774475381	snp	A/G	1.73138e-05	0.00294221	synonymous-codon	RAB40B	GRCh38.p7	17:82658699	CACCAGGATCTTGGG[A/G]ACTCCGGGGGCATGC	10966
rs774486477	snp	A/G	3.29516e-05	0.00405891	missense	RAB40B	GRCh38.p7	17:82658053	TGGCTTCTTAAGGCA[A/G]TGGGGAGCGGGAGCT	10966
rs774679478	snp	A/G	3.35329e-05	0.00409455	intron-variant	RAB40B	GRCh38.p7	17:82664447	GCTATGCCAGCCAGG[A/G]GGGTTACTCCCTGGG	10966
rs774756105	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668814	CGCAGGGAAGGCGGA[A/G]CTGCTGCCTGATCCG	10966
rs774791871	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82674588	AGCTTGCAGTGAGCC[A/G]AGATCGCGCCACTGC	10966
rs774792667	snp	C/T	3.31532e-05	0.0040713	missense	RAB40B	GRCh38.p7	17:82658578	CTGTGATGTTGAAAT[C/T]GCACAGAGGGCTGAC	10966
rs774842234	snp	C/T					GRCh38.p7	17:82654815	CTCAGCCTCCCAAAG[C/T]GTTAGGATTACAGAC	10966
rs774871985	snp	A/G	1.65625e-05	0.00287766	missense, downstream-variant-500B	RAB40B	GRCh38.p7	17:82661007	CGCCCCGGGAGTAGG[A/G]GCGGAATATGGTACA	10966
rs774938185	in-del	-/T					GRCh38.p7	17:82655952	GTCCCTTAAATTTCT[-/T]TTTTTTTTTTTTTTT	10966
rs774947726	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82662800	CCACTGGGCAGCTGG[C/G]GTCAGGGAGGCGTTC	10966
rs775131563	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82691517	ATGGTGAAACCCCCA[C/T]CTCTACTAAAAATAC	10966
rs775151640	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82693097	AACCTCCGCCTCCCG[A/G]GTTCAAGTGCTTCTC	10966
rs775152416	in-del	-/G			intron-variant	RAB40B	GRCh38.p7	17:82688590	CACAGCACTCCAGCT[-/G]GGTGACAAAGCGAGA	10966
rs775231505	snp	A/G	1.69994e-05	0.00291538	missense	RAB40B	GRCh38.p7	17:82658677	ACGCCAGGTGCAGGC[A/G]GTTCCCCACCAGGAT	10966
rs775239690	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82681758	AATGCAATTTATCAC[A/G]TCAATAAATCAAAAA	10966
rs775428303	snp	C/T	0.000116604	0.00763467	missense	RAB40B	GRCh38.p7	17:82658608	CCTCAAAGAAGGTCA[C/T]GCCCAGGCGCTCGGC	10966
rs775519675	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82667693	ATTAGACCAAGCAAC[A/G]CCAGAGCAAACTCCC	10966
rs775559201	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82683507	AAATAAGCAAAAGAG[C/G]CCAGACATAGTGGCT	10966
rs775617094	snp	A/T			intron-variant	RAB40B	GRCh38.p7	17:82678045	ATGTTCAAATTCAAT[A/T]TGTGAGAAGACTCTT	10966
rs775619838	snp	A/G	3.31263e-05	0.00406965	synonymous-codon, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660993	CTGTGTTACCTGTGC[A/G]CCCCGGGAGTAGGAG	10966
rs775626446	snp	G/T	4.19463e-05	0.00457945	utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698598	CCCAGGGCGCTCATC[G/T]TGACGGCCCGGCGCC	10966
rs775631714	snp	C/T	1.88255e-05	0.00306796	intron-variant, utr-variant-5-prime, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661094	AACCAGTGCTTCTTC[C/T]TGACAACAGGTTCTG	10966
rs775737880	snp	A/C	3.30628e-05	0.00406575	intron-variant	RAB40B	GRCh38.p7	17:82659680	AGAGGTCACAGGCTC[A/C]GCACGCAGAACACAG	10966
rs775845510	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82688548	TTGAAGCCGGGAGGC[A/G]GAGGGTGCAGTGAGC	10966
rs775897083	snp	A/T			intron-variant	RAB40B	GRCh38.p7	17:82659810	TGTAGCAGTTTTATG[A/T]TCATTTTCAGTGATA	10966
rs775899645	in-del	-/T	1.65715e-05	0.00287845	intron-variant	RAB40B	GRCh38.p7	17:82659543	ACGTCCTCCCAAGCC[-/T]ACAGGGATCTTGGGC	10966
rs775934631	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82677723	GCCCTACACAGAGCC[C/T]GCATCCTCTTTGCGC	10966
rs775939518	snp	A/C/G	8.53449e-05	0.00653194	missense, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698472	GCCGGGTGGCCGTAC[A/C/G]GGGACTCGGCCGCGC	10966
rs775946728	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82694312	AGCTAAGCAGATCAC[C/T]TGAGGTTAGGGGTTC	10966
rs776050585	in-del	-/TTTC	3.3089e-05	0.00406736	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657845	AGAGATTCCGCCGTG[-/TTTC]TTTCAGTGCCTTCCT	10966
rs776118016	snp	C/T	1.67351e-05	0.00289263	missense	RAB40B	GRCh38.p7	17:82658496	CTGGGCCTACCCTTG[C/T]TCGGCCGCCAGAGCC	10966
rs776119225	snp	C/T			downstream-variant-500B	RAB40B	GRCh38.p7	17:82656651	CCTTGTTGCCAGTGT[C/T]GTGTATTAGCTCCGA	10966
rs776146540	in-del	-/ATGT			intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660684	CGTACCTGCACACAC[-/ATGT]ACACACACACACACA	10966
rs776287072	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82682712	TAGAAATAGGCCCAC[A/G]CAAAAATGGCCAATT	10966
rs776305176	snp	C/T	7.51512e-05	0.00612943	missense, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698488	GGGACTCGGCCGCGC[C/T]ATCCTGCAGGCTCGC	10966
rs776374133	snp	G/T			intron-variant	RAB40B	GRCh38.p7	17:82683319	AAAACTGATCAACTG[G/T]ATTTCTTCAAAAGTA	10966
rs776376218	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669539	ACACCTGTCGTCCCA[A/G]CTTCTCAGGAGGCTG	10966
rs776380449	snp	C/T	2.00298e-05	0.00316457	missense, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698594	GCTGCCCAGGGCGCT[C/T]ATCGTGACGGCCCGG	10966
rs776466618	snp	A/T			intron-variant	RAB40B	GRCh38.p7	17:82687366	ATGTATATTTATGCC[A/T]CTGTAAACTTGTTTT	10966
rs776673725	in-del	-/T			intron-variant	RAB40B	GRCh38.p7	17:82686106	GCACCCAGCCTTCTT[-/T]TTTTTTTTTTTTTTT	10966
rs776927738	in-del	-/C			upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699930	TTCATCCCCTCCACC[-/C]TGCGTTGTGTAGGGA	10966
rs776962470	snp	C/T	6.60535e-05	0.00574651	synonymous-codon, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82664540	CAGCAGGATGGTGGT[C/T]GTCTTGTAGTCGATG	10966
rs777025532	snp	C/T			missense	RAB40B	GRCh38.p7	17:82657922	TCTGGGGGGGGCGGA[C/T]GAGCTTCACTTTGCG	10966
rs777038430	in-del	-/GGGGGGGCTCTG	3.50819e-05	0.00418804	cds-indel	RAB40B	GRCh38.p7	17:82657899	TCTGGTGCAGTTTTT[-/GGGGGGGCTCTG]GGGGGGGCGGACGAG	10966
rs777047317	snp	A/G	1.69519e-05	0.0029113	intron-variant	RAB40B	GRCh38.p7	17:82658146	AGCACTTGGGAGAGA[A/G]AAGATAAACCTTGCT	10966
rs777052219	snp	C/T	1.64811e-05	0.00287059	missense	RAB40B	GRCh38.p7	17:82658075	GCGGGAGCTTGTCCA[C/T]CAGGTGCACCGGCGT	10966
rs777074373	snp	A/C			intron-variant	RAB40B	GRCh38.p7	17:82680398	GGACGGCAGTTCCCC[A/C]ACGTGTGTGAGCTTC	10966
rs777097777	in-del	-/CA			intron-variant	RAB40B	GRCh38.p7	17:82660227	GATGCACACACAGTG[-/CA]CACACGCAGTTCATG	10966
rs777142831	in-del	-/C	1.65181e-05	0.00287381	intron-variant	RAB40B	GRCh38.p7	17:82659572	GCAGTGGCATTTCTA[-/C]AACATACCTCATCGA	10966
rs777148822	in-del	-/CT			intron-variant	RAB40B	GRCh38.p7	17:82672179	TAACTCTAACACACA[-/CT]CACATGCTCCCTGTA	10966
rs777152530	snp	A/T	1.88e-05	0.00306588	missense, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698581	AGGCCCGGACCGGGC[A/T]GCCCAGGGCGCTCAT	10966
rs777231823	snp	C/T	1.68923e-05	0.00290618	intron-variant, missense, downstream-variant-500B	RAB40B	GRCh38.p7	17:82661058	TATCCCTGGAAAAGA[C/T]GTTGGAGACCATTAA	10966
rs777236381	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82686203	TGAAACCTCCGCTTC[C/T]GGGGTTCAAGTGATT	10966
rs777283212	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82658406	TGAGACGGGTCCCGG[C/G]AGGCAGACACTTATC	10966
rs777321865	snp	A/G	1.64814e-05	0.00287061	missense	RAB40B	GRCh38.p7	17:82657919	GGCTCTGGGGGGGGC[A/G]GACGAGCTTCACTTT	10966
rs777354767	in-del	-/C	2.33877e-05	0.00341955	utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698612	CGTGACGGCCCGGCG[-/C]CCCCACCCATGCCCG	10966
rs777402534	snp	A/C/G			intron-variant	RAB40B	GRCh38.p7	17:82672216	TGACACACCCCACCC[A/C/G]TGTAACTCTAACACA	10966
rs777425841	in-del	-/CCAGGATCT	1.70651e-05	0.00292101	cds-indel	RAB40B	GRCh38.p7	17:82658686	GCAGGCGGTTCCCCA[-/CCAGGATCT]TGGGGACTCCGGGGG	10966
rs777425920	snp	C/G/T	0.00177438	0.0297427	synonymous-codon, missense	RAB40B	GRCh38.p7	17:82657908	GTTTTTGGGGGGGCT[C/G/T]TGGGGGGGGCGGACG	10966
rs777620647	snp	A/G	1.65855e-05	0.00287967	intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660971	TGATCTCCCAGCTCG[A/G]GGGATGCTGTGTTAC	10966
rs777681157	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82683036	TAATCCCAGGTACTC[A/G]GGAGGCTGAGGCAGG	10966
rs777684363	snp	A/C			intron-variant	RAB40B	GRCh38.p7	17:82689481	GGCTGGGGTTACAGA[A/C]GTAACAGGTCAAGCT	10966
rs777774348	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82677729	CACAGAGCCCGCATC[C/T]TCTTTGCGCAGGACA	10966
rs777790794	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82678382	TGTTCACTGAGTGAG[C/T]CAGAAAACAGGGACA	10966
rs777796278	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82667134	GCTCCTCTAAAAATG[C/T]GAGGCTGCGGAGGCC	10966
rs777880422	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669976	GCAGGCACGAGGCAA[C/T]GAACGAATACACTTG	10966
rs777904019	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82660135	CACACGTGTACACAC[A/G]TGTACTCATGCACAG	10966
rs777989777	snp	A/G	4.97665e-05	0.00498806	intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660970	TTGATCTCCCAGCTC[A/G]GGGGATGCTGTGTTA	10966
rs778024108	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82674443	GAGACCATCCTGGCT[A/G]ACAGGGTGAAACCCC	10966
rs778090149	snp	A/G	1.65839e-05	0.00287953	intron-variant	RAB40B	GRCh38.p7	17:82664581	GGTTAGAGACGGCTT[A/G]GGCCTGAGGCTGCAG	10966
rs778095790	snp	C/T	9.77119e-05	0.00698902	synonymous-codon, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698456	CCGCCCGCGCTCACC[C/T]GCCGGGTGGCCGTAC	10966
rs778214921	in-del	-/ACAT			intron-variant	RAB40B	GRCh38.p7	17:82694557	AATACATACACACAC[-/ACAT]ACACACACACACCTG	10966
rs778276549	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82684986	GGGCGTGGTGGCAGG[C/T]GCCTATAATCCCAGC	10966
rs778280721	in-del	-/CCTGTGCAGCG			intron-variant	RAB40B	GRCh38.p7	17:82667436	CCTGATCTGAGCACA[-/CCTGTGCAGCG]CCTGTGCAGCGCCTT	10966
rs778283673	snp	A/C/G	4.25362e-05	0.00461158	intron-variant	RAB40B	GRCh38.p7	17:82658758	GGGTTACTTCAGTGA[A/C/G]ATTTTGTTGTCGTCG	10966
rs778358667	snp	G/T			intron-variant	RAB40B	GRCh38.p7	17:82663818	TCCCACAGACACCAG[G/T]CCACAGGTTCTGATC	10966
rs778367753	snp	A/C	3.5108e-05	0.0041896	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657745	CGGAAGGCGTCGCAC[A/C]CATTCGCAAGCAGCA	10966
rs778370479	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82686300	TATTTTTAGTAGAGA[C/T]GGGATTTCCCCATGT	10966
rs778371293	snp	A/T			intron-variant	RAB40B	GRCh38.p7	17:82675475	ACTCCCTTTACCCCA[A/T]ACTTCAGAACTGGGG	10966
rs778408084	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82685384	AGATTCCTGGGGCCT[C/T]CTTGGAGTCACCAAG	10966
rs778471205	snp	C/T	1.65919e-05	0.00288022	intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660967	GGTTTGATCTCCCAG[C/T]TCGGGGGATGCTGTG	10966
rs778566656	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82676504	CACCAATTCCGTGGC[A/G]AGTCTCTCGGCTCTT	10966
rs778583935	snp	A/C/G	3.29996e-05	0.00406189	missense	RAB40B	GRCh38.p7	17:82659650	ATGTCATAGACCAGG[A/C/G]TCACACCCTGGGGGA	10966
rs778630457	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82680849	AGCCTGGATAACATG[A/G]TGAAACCCCGTCTCT	10966
rs778659354	snp	A/C	1.65299e-05	0.00287483	missense	RAB40B	GRCh38.p7	17:82658113	ACGACCGCCCGGCAG[A/C]AGAGGTCTTGCAAGC	10966
rs778848822	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82693767	TCTCTTTCACATAAC[A/G]GGGGCCAGAGACACA	10966
rs778912611	snp	A/G			intron-variant, utr-variant-5-prime, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661199	ACAAAACTTTCCAAT[A/G]TCCCTGAAGGGATCC	10966
rs778941916	snp	A/G	1.70374e-05	0.00291863	intron-variant	RAB40B	GRCh38.p7	17:82658447	CTGACCCACCTCGGC[A/G]TCTGGAGGGCAGAGG	10966
rs779131285	snp	A/G	1.65578e-05	0.00287726	intron-variant	RAB40B	GRCh38.p7	17:82664567	GATGCCTGCGGAAGG[A/G]TTAGAGACGGCTTAG	10966
rs779145452	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82690660	TGTTCCCGGGGAGCA[A/G]AGAGTGTGCACGTGT	10966
rs779231827	in-del	-/TG			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671332	CACTCACACGCTCTC[-/TG]TGTACTGACACACCT	10966
rs779235470	snp	A/G	1.90214e-05	0.00308388	intron-variant	RAB40B	GRCh38.p7	17:82658732	GCGGGCAGGAGAAAG[A/G]CGAGGAGCATGGGTT	10966
rs779243980	snp	C/T	0.000154637	0.00879174	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657704	TAGAAATTCGAAGTC[C/T]GACGGGGTAGTGTGT	10966
rs779250836	in-del	-/T			intron-variant	RAB40B	GRCh38.p7	17:82679235	AACCACCTTCTCCGG[-/T]AGCCTGAAGGACACC	10966
rs779321901	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82670905	TCATGGAGTCATGGA[C/T]GCTCACAGTCTGAAG	10966
rs779371856	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82695172	GGAGTTACGAACGCC[C/T]TCATCTTTCTTTCTT	10966
rs779428324	snp	A/G	4.41667e-05	0.00469908	utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698634	CCATGCCCGGCCTGC[A/G]GGGCTGAGCGCAGAG	10966
rs779437437	snp	C/G	1.69657e-05	0.00291248	missense	RAB40B	GRCh38.p7	17:82658647	GGGCCTGCTCCGTGG[C/G]CACCTGCCGCTTGAA	10966
rs779486995	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82683095	TTGCAGTGAGCCGAG[A/G]TCATGCCACTGCATT	10966
rs779516020	in-del	-/GAA			intron-variant, downstream-variant-500B, utr-variant-5-prime	RAB40B, MIR4525	GRCh38.p7	17:82668000	ACCTCTGTGGCTGCT[-/GAA]GAATTATTGTCCTGC	10966
rs779526883	in-del	-/AAAAAAAAAAAAA			intron-variant	RAB40B	GRCh38.p7	17:82681022	CAAGACTCCATCTCA[-/AAAAAAAAAAAAA]AAAAAAAAAAAAAAA	10966
rs779598697	snp	C/T					GRCh38.p7	17:82655342	GGCCTCCGGGCGGCC[C/T]GTGCATTCGGTGAAC	10966
rs779694195	snp	G/T	1.64972e-05	0.00287199	missense	RAB40B	GRCh38.p7	17:82659630	CAAAAGACCAGCGGT[G/T]CGCAATGTCATAGAC	10966
rs779766637	snp	G/T			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669107	CTTTGGGAGGTTAAG[G/T]TGAGAGGATCGCTTG	10966
rs779775946	in-del	-/A			intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661888	GAGACTCTGTCTCAG[-/A]AAAAAAAAAAAAAAA	10966
rs779871932	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82686561	CGACAGACAGCAGGG[A/G]CTGGAACGGTGCTGC	10966
rs779933620	snp	A/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82672007	TCACCCCTGTAACTC[A/T]AACACACACACACGC	10966
rs780045248	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82692377	GGAGAATCCAGGCCT[C/T]GCTGACCGTATCGGA	10966
rs780045867	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82658767	CAGTGAGATTTTGTT[A/G]TCGTCGTAATGTGGG	10966
rs780136299	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82659353	ACGCCGTGGACGCTC[A/G]TTTCGTCTGGACCAG	10966
rs780172202	snp	G/T			intron-variant	RAB40B	GRCh38.p7	17:82682064	AAGAAAGAAAAGGCA[G/T]GCAGATTAAAACCAT	10966
rs780248753	snp	A/C			intron-variant	RAB40B	GRCh38.p7	17:82697418	CAGACCCTTCCCAGG[A/C]CCCAGAGCTGACAGG	10966
rs780357956	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668469	CTTGTTCATGCCAAG[A/G]GGCGCCTGCAGGCCA	10966
rs780381604	snp	A/G			intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660876	ACCAATTTATACGTA[A/G]GCTTAACCGCCTTGT	10966
rs780395199	snp	C/G	1.65633e-05	0.00287774	missense	RAB40B	GRCh38.p7	17:82658561	CAGCTCCGTGAACGA[C/G]TCTGTGATGTTGAAA	10966
rs780397067	snp	A/C/G	0.000364001	0.0134864	utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698627	CCCCCACCCATGCCC[A/C/G]GCCTGCGGGGCTGAG	10966
rs780529374	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82685988	TTTGTATTTTTAGTA[C/G]AGACGGGGTTTCACC	10966
rs780547736	snp	C/G			intron-variant, utr-variant-5-prime, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661232	GTGTTGGGATGTCCT[C/G]CCAGGCTCATGCTCT	10966
rs780591135	snp	A/G	5.3425e-05	0.00516814	synonymous-codon, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698558	CAGGAACTTGAGCAG[A/G]AAGTCGTAGGCCCGG	10966
rs780592778	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82677575	CAGCCCTGACGCCGC[A/G]TCTCTGTCCCTGTGG	10966
rs780642744	snp	A/G/T	3.29675e-05	0.00405991	synonymous-codon	RAB40B	GRCh38.p7	17:82657917	GGGGCTCTGGGGGGG[A/G/T]CGGACGAGCTTCACT	10966
rs780645091	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82673915	TCTTGTCTGATTTTG[C/G]ATCTCTCTCTCTTTT	10966
rs780684539	snp	A/G			intron-variant, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82696509	TGTAGCTCTGGTAGG[A/G]TTCATCCCTCACTGA	10966
rs780805427	snp	C/G			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82666154	TTGCTGTGTTGCCCA[C/G]GCTGGTCAACCTCCT	10966
rs780818361	snp	G/T					GRCh38.p7	17:82656342	GTTTAGTCCCTCATT[G/T]GCGACCCCCAGCCAC	10966
rs780821630	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82695231	AAAATCTCACTCTGT[C/T]GCTGGGCTGGAGTGC	10966
rs780865135	in-del	-/T	0.000158844	0.00891048	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657645	AGTACTAATTTTCCC[-/T]TTACAAACACACATC	10966
rs780947239	snp	C/T	1.65608e-05	0.00287752	intron-variant	RAB40B	GRCh38.p7	17:82664492	GCACCTCCTCCAGAC[C/T]CACCAGAGCTGCAGC	10966
rs780949117	snp	A/G	3.29495e-05	0.00405877	missense	RAB40B	GRCh38.p7	17:82657930	GGGCGGACGAGCTTC[A/G]CTTTGCGGAGGCTGC	10966
rs780987906	in-del	-/CTGGGCCTACCCTTGCTCGGCCGCCAGAGCCGGTCCATCCCATG	0.000337029	0.0129769	intron-variant	RAB40B	GRCh38.p7	17:82658480	CCCCCGGAATAGCCC[lengthTooLong]CTGGGCCTACCCTTG	10966
rs780993033	snp	C/T			utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657490	ATTATCCCGCTGCCA[C/T]TGCTTCTCAAATTCC	10966
rs781000834	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668788	CTGCCCCAGGGCAGC[A/G]GGCCGCGGCACGCAG	10966
rs781039510	snp	A/G	0.000112039	0.00748376	utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698644	CCTGCGGGGCTGAGC[A/G]CAGAGGCGGCGGCCC	10966
rs781143480	snp	G/T	5.2633e-05	0.00512969	intron-variant, utr-variant-5-prime, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661077	GGAGACCATTAAGAA[G/T]AAACCAGTGCTTCTT	10966
rs781156914	in-del	-/TTT			intron-variant	RAB40B	GRCh38.p7	17:82686104	CCGCACCCAGCCTTC[-/TTT]TTTTTTTTTTTTTTT	10966
rs781168886	in-del	-/GT			intron-variant, downstream-variant-500B	RAB40B	GRCh38.p7	17:82660693	CACACATGTACACAC[-/GT]ACACACACACACAGG	10966
rs781203374	snp	C/G			intron-variant	RAB40B	GRCh38.p7	17:82688057	AGCCTGGGCAATAAG[C/G]CAGACCCGGTTTCAA	10966
rs781212028	snp	A/C	1.67649e-05	0.0028952	missense	RAB40B	GRCh38.p7	17:82658491	AGCCCCTGGGCCTAC[A/C]CTTGCTCGGCCGCCA	10966
rs781213834	snp	A/C	7.55373e-05	0.00614515	utr-variant-3-prime	RAB40B	GRCh38.p7	17:82657682	AAGAGCTTCATGCAC[A/C]TCCACGTAGAAATTC	10966
rs781220141	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82689249	CAGGTGCGGCTGGCA[A/G]GATGAGGCAGGACTG	10966
rs781221549	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82681621	TAAAATAACTTACTA[C/T]ACAATAAATTAAAAG	10966
rs781310286	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82682094	TCTCGATTACCAGAT[A/G]ACATTACTATACACA	10966
rs781402831	snp	A/G	2.801e-05	0.00374222	missense, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698460	CCGCGCTCACCCGCC[A/G]GGTGGCCGTACGGGG	10966
rs781414239	snp	C/T	1.76608e-05	0.00297155	synonymous-codon, utr-variant-5-prime	RAB40B	GRCh38.p7	17:82698537	CACGTCGCTGTCGCC[C/T]ACCAGCAGGAACTTG	10966
rs781460458	snp	A/G					GRCh38.p7	17:82655210	GTAGCTCTGGAAGCC[A/G]GAAGTCCAAAACCAA	10966
rs781464100	snp	G/T			stop-gained, downstream-variant-500B	RAB40B	GRCh38.p7	17:82661002	CTGTGCGCCCCGGGA[G/T]TAGGAGCGGAATATG	10966
rs781499958	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82659382	AGCTTCCTGAGCTTT[C/T]GTGATTGTAGCTATC	10966
rs781504009	snp	A/G	1.65636e-05	0.00287776	missense	RAB40B	GRCh38.p7	17:82658553	ATCCTGGCCAGCTCC[A/G]TGAACGACTCTGTGA	10966
rs781514245	in-del	-/CTT			intron-variant	RAB40B	GRCh38.p7	17:82673846	ATAATTTGTTCTCTC[-/CTT]CTGGGATGTGATTAA	10966
rs781736312	snp	A/C			intron-variant	RAB40B	GRCh38.p7	17:82663418	AGGATGAGGCACCGC[A/C]GGAGCCCCCCATCCC	10966
rs796137110	snp	A/G			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82669599	TGGAGACTGCAGTCA[A/G]CTATGATCGTGCCAC	10966
rs796163835	in-del	-/AC			intron-variant	RAB40B	GRCh38.p7	17:82660544	ACAGTGCACATACCT[-/AC]ACACACGTGTACACA	10966
rs796164311	snp	G/T			upstream-variant-2KB	RAB40B	GRCh38.p7	17:82699820	CCCTTCGCTCTGAGG[G/T]TCTCACCAGGTGCAC	10966
rs796195513	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82688671	GGGCGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC	10966
rs796205456	snp	A/T			intron-variant	RAB40B	GRCh38.p7	17:82672732	AACCTTGGACTTCCC[A/T]GCCTCCAGAACTGTA	10966
rs796238176	snp	A/G			downstream-variant-500B	RAB40B	GRCh38.p7	17:82656615	CCTTTCTCAACAGGC[A/G]ACAACAGTTCAAGGA	10966
rs796244010	in-del	-/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82665270	CTTCTTTTTTTTTTT[-/T]GAGACAGAGTTTCTC	10966
rs796272335	in-del	-/A			intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661909	AAAAAAAAAAAAAAA[-/A]GGAAGAAACAAATGA	10966
rs796276411	snp	A/G			intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82661640	ACCGATAATCCCAGC[A/G]CTTTGGGAGACCGAG	10966
rs796290213	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82679827	GGACACCTGGAAACA[C/T]GAAGGAACACGGCCC	10966
rs796329780	in-del	-/GCAC			intron-variant	RAB40B	GRCh38.p7	17:82660036	CACTTGTGCACAGAT[-/GCAC]GCACACACAGTGCAC	10966
rs796358128	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82660045	ACAGATGCACGCACA[C/T]ACAGTGCACGTACCT	10966
rs796376613	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82673455	GGATTCCATCCTTCC[C/T]TCTCTTAAGCTGACT	10966
rs796401397	in-del	-/G			intron-variant	RAB40B	GRCh38.p7	17:82663261	CGTAGGAAGGGGACA[-/G]GTAAGAGAAGGGGGT	10966
rs796414868	in-del	-/TT			intron-variant	RAB40B	GRCh38.p7	17:82686105	CCGCACCCAGCCTTC[-/TT]TTTTTTTTTTTTTTT	10966
rs796416532	multinucleotide-polymorphism	ATC/CTA			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671442	ACACGCTCCCTGTAC[ATC/CTA]CTGACACACCCCACC	10966
rs796443032	snp	C/T			intron-variant, utr-variant-3-prime	RAB40B	GRCh38.p7	17:82662158	GGTGACCACCCTCAG[C/T]ACGAGAGAGAAGGGC	10966
rs796638588	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82678752	CTGGACAGCACAGGG[C/T]TCCTGGAAGTGGCCG	10966
rs796680677	in-del	-/A			intron-variant	RAB40B	GRCh38.p7	17:82673463	TCCTTCCCTCTCTTA[-/A]GCTGACTCCTCTTTT	10966
rs796685634	in-del	-/AC			intron-variant	RAB40B	GRCh38.p7	17:82660555	CCTACACACACGTGT[-/AC]ACACACACACACGCA	10966
rs796702897	snp	A/C			intron-variant, upstream-variant-2KB	RAB40B, MIR4525	GRCh38.p7	17:82668376	CCCCCTTGAAGCTTC[A/C]AGGTGTGGCTTCACC	10966
rs796707519	snp	A/G					GRCh38.p7	17:82655293	ACATGTTCCGCTTCT[A/G]GGGACTTCTGGTGGT	10966
rs796708923	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671992	ACCCACTGACACAGC[C/T]CACCCCTGTAACTCT	10966
rs796729512	in-del	-/AC			intron-variant	RAB40B	GRCh38.p7	17:82660353	CCTGCACGCACGTGT[-/AC]ACACACACACGCACA	10966
rs796768394	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82686291	TAATTTTTGTATTTT[C/T]AGTAGAGATGGGATT	10966
rs796776183	snp	C/T			upstream-variant-2KB	RAB40B	GRCh38.p7	17:82700119	AACACCTGTTATTCA[C/T]TGGTTGATTAGTTGC	10966
rs796783978	snp	C/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82672025	CACACACACACGCTC[C/T]CTGTACTCACTGACA	10966
rs796800917	snp	A/G			intron-variant	RAB40B	GRCh38.p7	17:82695394	ATAGGGTTTCACCAT[A/G]TTGACCAGGCTGGTC	10966
rs796836945	snp	C/T			intron-variant	RAB40B	GRCh38.p7	17:82698016	CCCGGAGCTCGCGTC[C/T]CCTCCCGCCCCTCCT	10966
rs796845678	in-del	-/CA			intron-variant	RAB40B	GRCh38.p7	17:82682121	ACACACACACGCATG[-/CA]CACACACACACACAC	10966
rs796872706	snp	G/T			intron-variant	RAB40B	GRCh38.p7	17:82686303	TTTTAGTAGAGATGG[G/T]ATTTCCCCATGTTGG	10966
rs796882052	in-del	C/TT					GRCh38.p7	17:82655953	CCCTTAAATTTCTTT[C/TT]TTTTTTTTTTTTTAG	10966
rs796892777	snp	A/C			intron-variant	RAB40B	GRCh38.p7	17:82672099	CTCACTGACACACCC[A/C]ACCCCTGTAACTCTA	10966
rs796925148	in-del	-/AC			intron-variant	RAB40B	GRCh38.p7	17:82672171	ACCCCTGTAACTCTA[-/AC]ACACACACTCACATG	10966
rs796982666	snp	A/T			intron-variant, upstream-variant-2KB	RAB40B	GRCh38.p7	17:82671909	CCACCCCTGTAACTC[A/T]AACACACACTCACAT	10966
rs796995765	snp	G/T			intron-variant	RAB40B	GRCh38.p7	17:82658230	TCCCGCCCTCCCAAG[G/T]CTCGGACGCCCGTGG	10966
rs797013955	snp	A/C			intron-variant	RAB40B	GRCh38.p7	17:82676422	GTGAGGGCACCCCTC[A/C]CCTTCAACAGCCTCT	10966

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