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

MYO1F

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs189088448	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8560395	GAGGCTGAGGCAGGA[A/G]ACTCGCTTGATCCCG	4542
rs189096925	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8523157	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC	4542
rs189337130	snp	C/T	0.00318978	0.0398085	intron-variant	MYO1F	GRCh38.p7	19:8560898	CGCCCGCCACCACGG[C/T]GGCTAATTTTTTGTA	4542
rs189341006	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8535367	AAATCAAAATCTATA[A/G]ACTGAAATTTTTGTC	4542
rs189341272	snp	A/T	0.0263992	0.111815	intron-variant	MYO1F	GRCh38.p7	19:8538140	TTTTTTTATATATAT[A/T]TTTTTAGTAGAGACG	4542
rs189346453	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8574138	CAGCTGAAAACAATC[C/T]ACCACCAACGAACAA	4542
rs189470739	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8552479	ATCATGTTGGCCAGG[C/G]TGGTCTTGAACTCCA	4542
rs189476212	snp	A/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8569549	GGCCCCTACTGTGCA[A/T]GGAGGTAGGTGGAGA	4542
rs189514109	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8534975	TGAGTGCAGTGGCAC[C/G]ATCTTGGCTCACTTC	4542
rs189584296	snp	A/G	0.00993419	0.0697739	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578980	CATGCAATTCTCAGC[A/G]ATGTCTCCAGGCACT	4542
rs189861458	snp	A/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8557665	TACCCCTCACTTCCC[A/T]TGAAGGATGCCAGGC	4542
rs189869971	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530099	AACAGATGGATCTAG[A/G]CTGGGGGATATCTGG	4542
rs189909397	snp	C/T	0.0295035	0.117819	intron-variant	MYO1F	GRCh38.p7	19:8551341	ACAGGTGTGAGCCAC[C/T]GTGCCTGGCCTTTTT	4542
rs189958890	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8563089	CTCTGCCTCCCGGGT[C/G]CAAGTGATTGTCCTG	4542
rs189988284	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8545269	ATTTTTTGTATTTTT[A/G]GTAGAGACAGGTTTT	4542
rs189992688	snp	A/G	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8526806	GTCGCTGAAGGTGAG[A/G]GGCAGGGGCCTCCGC	4542
rs190114637	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8566413	ATCTCATGATCCACC[C/T]GCCTCGGCCTCCCAA	4542
rs190129837	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8569072	GGCATCAGTGTTGGA[C/T]AGAAAGCCTGGTCAA	4542
rs190144113	snp	G/T	0.0111196	0.0737302	intron-variant	MYO1F	GRCh38.p7	19:8531028	CAGCCTGGACAACAA[G/T]AGTGAAACTCCATCT	4542
rs190161519	snp	A/G	0.0471551	0.14613	intron-variant	MYO1F	GRCh38.p7	19:8534166	CCTGGGTGACAGAGC[A/G]AGACTCTGTCTAAAA	4542
rs190199003	snp	A/G	0.00438332	0.0466095	intron-variant	MYO1F	GRCh38.p7	19:8560213	TTCTTGGCTGGGCGC[A/G]GTGGCTCACGCCTGT	4542
rs190225305	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8523381	ACATGGTCTCACTCT[C/T]GCCCAGGTTGGAGTG	4542
rs190233335	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8541376	AAGGATCCCCGTCTT[A/G]TTACTTTACATCTAA	4542
rs190237512	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8567594	ACTCCCAACCTCAGG[C/T]GATCCTCCCACCTCG	4542
rs190411389	snp	C/T	0.00795532	0.062565	intron-variant	MYO1F	GRCh38.p7	19:8547176	CATGATGGTGTGTGC[C/T]TGCGGTCCCAGCTAC	4542
rs190471455	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8563501	ACAGGATTTTTCTTT[G/T]TCTTTCTTTCTTTCT	4542
rs190474061	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8545556	TAGAGAAGGGCCTGA[A/G]GATGCCATAACACCC	4542
rs190602258	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8574968	GCCATGTTGGCCAGG[C/G]TGGTCTTGAACTCTT	4542
rs190618876	snp	A/G/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8562387	ATCATACCTCACTGC[A/G/T]GCCTCGAACTCCTGG	4542
rs190626111	snp	C/T	8.40343e-05	0.00648152	intron-variant	MYO1F	GRCh38.p7	19:8539926	GCAGGCCCAGCTCCC[C/T]GTTGTACACCCCAGG	4542
rs190628244	snp	A/G	0.0217236	0.101931	intron-variant	MYO1F	GRCh38.p7	19:8523309	AAGTGCTGGGATTAC[A/G]GGCATGAGCCACCGC	4542
rs190637191	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8523322	ACAGGCATGAGCCAC[C/T]GCGCCTGGCCAATTA	4542
rs190644696	snp	A/G	0.00358779	0.0422022	intron-variant	MYO1F	GRCh38.p7	19:8559245	TACAGGCAGGGCACA[A/G]GCAGAAGTGTCCACG	4542
rs190651878	snp	A/G/T			intron-variant	MYO1F	GRCh38.p7	19:8559868	GGCAGGAGAATCGCT[A/G/T]GAACCCAGGAGGCGG	4542
rs190847721	snp	A/G	0.00636936	0.0560724	intron-variant	MYO1F	GRCh38.p7	19:8571889	GGTGTAAGCCACCGC[A/G]CCCAGCCCCTGTATT	4542
rs190856721	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8572014	AGGCGTAAGCCACCG[C/T]GCCTGGCCTTTATAC	4542
rs190869814	snp	C/G	0.00318978	0.0398085	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8536211	TATACCTTTCTCTCT[C/G]TTCCCCTCTCCTTCT	4542
rs190872672	snp	C/T	0.00597247	0.0543191	intron-variant	MYO1F	GRCh38.p7	19:8576054	CAGGCTGGAGTGCAG[C/T]GGCAGGATCTCAGCT	4542
rs190898847	snp	A/G	0.00676609	0.0577691	intron-variant	MYO1F	GRCh38.p7	19:8537206	GGGCCAGATGTCCCT[A/G]GTCTGTGTGCACCTC	4542
rs190907121	snp	C/T	0.00636936	0.0560724	intron-variant	MYO1F	GRCh38.p7	19:8540664	GCAGTGAGCCGAGAT[C/T]GTGCCACTGCACTCC	4542
rs190908621	snp	A/G	0.00614226	0.0550763	utr-variant-3-prime	MYO1F	GRCh38.p7	19:8521494	GGCAGGCAGATAGGC[A/G]GGCGAAAGAGAAGGC	4542
rs191123434	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8533685	TTAAAACCTTTAGAG[A/G]GTATGGCCATGCCAA	4542
rs191128252	snp	A/G	2.8746e-05	0.00379106	intron-variant	MYO1F	GRCh38.p7	19:8550400	GGGACAGTTGGTTGG[A/G]CTCTTGTGCCTCCTG	4542
rs191148063	snp	A/G	0.00557542	0.0525036	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8577509	TGGGGGAGGGAAGCT[A/G]GGTGTGGAGGGGGGC	4542
rs191148523	snp	C/G/T	0.0318376	0.122163	intron-variant	MYO1F	GRCh38.p7	19:8555526	CCCTGCTGTCACTCT[C/G/T]TCTGTCCTCTGTGTC	4542
rs191158671	snp	C/T	0.00199481	0.0315187	intron-variant	MYO1F	GRCh38.p7	19:8548830	CCTGACCTCGTGATC[C/T]GCCCGCCTCGGCCTC	4542
rs191361758	snp	C/T	0.00318978	0.0398085	intron-variant	MYO1F	GRCh38.p7	19:8546433	GATGCGATCCTAGCT[C/T]ACTGCAACCTTGACC	4542
rs191366039	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8529336	CCCAGGTACAGGTGA[C/T]GGTAAACAGGCCAAG	4542
rs191378682	snp	A/G	0.00478085	0.0486577	intron-variant	MYO1F	GRCh38.p7	19:8565970	AAAAATTAGCCAGGC[A/G]TGGTGGTATGCGCCT	4542
rs191436386	snp	A/C	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8531951	GGTGAAACCCCGTCT[A/C]TACTAATAATACAAA	4542
rs191437652	snp	G/T	0.00279162	0.0372561	intron-variant	MYO1F	GRCh38.p7	19:8553736	AATTAGCCGGACATG[G/T]TGGTGGGCGCCTGTA	4542
rs191454151	snp	C/T	0.00597247	0.0543191	intron-variant	MYO1F	GRCh38.p7	19:8527899	ATTACAGGTGTGCGC[C/T]ACCACGCCTGGCCAT	4542
rs191517493	snp	G/T			downstream-variant-500B	MYO1F	GRCh38.p7	19:8520412	CATTTTCCTGCCTCA[G/T]CCTCCCGAGCAGCTG	4542
rs191582666	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578998	GTCTCCAGGCACTCA[A/G]GAGTGAATATGAATG	4542
rs191693528	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8535711	TTGAGACGGAGTCTC[G/T]CTCTGTCGCCCAGGC	4542
rs191697282	snp	A/C	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8533336	GCCCAGCCTCAGATT[A/C]TTCTTCTTCTTCTTC	4542
rs191704219	snp	C/G	0.00358779	0.0422022	intron-variant	MYO1F	GRCh38.p7	19:8567793	GTCTGTATCAGAGAT[C/G]GCCGGGGTTGCTGCT	4542
rs191959738	snp	A/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8556122	CAACATCCACCTCCC[A/G]GGTTCAAGCGATTCT	4542
rs191981941	snp	C/T	5.06727e-05	0.00503327	missense	MYO1F	GRCh38.p7	19:8522457	TACTGGTATAGGGCC[C/T]GGCACCTGGGACCAT	4542
rs191983095	snp	C/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8544739	AAGAGATTCAGGCCC[C/G]AGACTAGAATCCCTT	4542
rs191988990	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8549575	TGGAATACAATAGCA[C/T]GATCTCAGCTCACTG	4542
rs192005639	snp	A/G	0.00874735	0.0655527	intron-variant	MYO1F	GRCh38.p7	19:8537791	CTGGGGTATAGTGGC[A/G]CCGTGATAGTTCACT	4542
rs192155328	snp	C/T	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8560409	AGACTCGCTTGATCC[C/T]GGGAGGCAGAGGTTG	4542
rs192241494	snp	G/T	0.00358779	0.0422022	intron-variant	MYO1F	GRCh38.p7	19:8541630	GACAAGGTTTTGCCA[G/T]GTTGCCCAGGCTGGT	4542
rs192246615	snp	A/G	0.00676609	0.0577691	intron-variant	MYO1F	GRCh38.p7	19:8560343	CAAAAAAAGTAGCCG[A/G]GTGTGGGGGTGCGCG	4542
rs192250045	snp	A/G	0.00676609	0.0577691	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8577831	GTTTGAGACCAGCCT[A/G]GGCTATATAGCATGA	4542
rs192256753	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8534629	TATTTTCATTTTACT[A/G]ATTTTTTTTTTTTTG	4542
rs192293117	snp	C/T	0.0023933	0.0345097	intron-variant	MYO1F	GRCh38.p7	19:8525972	TTTTGATTGGTTTCC[C/T]CCATGGCCACGTCCC	4542
rs192470480	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8556463	CCTGGGCAACATAGC[A/G]AGGCCCCGTCTCTAT	4542
rs192474834	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8573246	AACCTAGGAGGTGGG[A/G]CTTGCAGTGAGCCAA	4542
rs192497409	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8523058	TTTTTTTGAGATGGA[A/G]TCTTGCTCAGTCGCT	4542
rs192527473	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8542736	CTCCCGATGAGCTGG[C/G]ATTACAGGCGTGTGC	4542
rs192537049	snp	A/T	0.00199481	0.0315187	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578263	CCTGCCTCAGCCTCC[A/T]GAGTAGCTGGGATTA	4542
rs192688329	snp	C/T	0.00597247	0.0543191	intron-variant	MYO1F	GRCh38.p7	19:8551093	GTCTCACTCTTTCAC[C/T]CAGGCGGGAGTGCAG	4542
rs192700861	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8563204	CACCATGTTGGTCAG[G/T]CTGGTCTTGAACTCC	4542
rs192771381	snp	C/T	0.00199481	0.0315187	intron-variant	MYO1F	GRCh38.p7	19:8521805	TCCGGCCATTTCTAC[C/T]CTTTAAAAGTTTTTT	4542
rs192794421	snp	C/T	0.00835141	0.0640778	intron-variant	MYO1F	GRCh38.p7	19:8566236	GCAGTGGCATGATCT[C/T]GGCTCACTGCAAGCT	4542
rs192805660	snp	A/G/T	5.01878e-05	0.00500913	missense, synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8530538	TCGGGCAAAGCCATC[A/G/T]AACTTTCGCTCTCGC	4542
rs192878329	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8568547	GTGATGGATTGGGGT[C/T]AAAGCCTGGCTTGAC	4542
rs192890343	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8533910	AAAATAGGGGCCGGG[C/T]GCGGTGGCTCATGCA	4542
rs192933995	snp	A/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8569325	TCTTGTGAAAGGCAG[A/T]CAGGGGCTTGAGGTG	4542
rs193014972	snp	A/G	0.00597247	0.0543191	intron-variant	MYO1F	GRCh38.p7	19:8572775	ATCACAGCTCACTGC[A/G]GCCTGGAACTCCTGG	4542
rs193023191	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8546711	GACAGGGTCTCATTC[C/T]GCTGTTGCCCAGGCT	4542
rs193077776	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8546228	TGCCACCACGCCGGA[A/C]TAATTTTGTATTTTT	4542
rs193178220	snp	C/T	0.000264945	0.0115066	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8552054	GTAGATGTGGAAGTT[C/T]CTCTCATTTTCATTT	4542
rs193185441	snp	C/T	0	0	intron-variant	MYO1F	GRCh38.p7	19:8523854	GGCTAGGCGCGGTGG[C/T]TCACGCCTGTAATCC	4542
rs193251926	snp	A/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8528390	AAAACTAGCTGGGCG[A/T]GGTGGCACATGCCTG	4542
rs199542866	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8524583	GAGCGAGACTGTCTC[A/C]AAAAAAAAAAAAAAA	4542
rs199561792	snp	A/T	1.84759e-05	0.00303935	intron-variant	MYO1F	GRCh38.p7	19:8525573	AGGCTCTGAAAGAAG[A/T]GTGTCAGGGAGTTGA	4542
rs199570120	in-del	-/ACG			intron-variant	MYO1F	GRCh38.p7	19:8544727	GGGGACCCCTCAAGA[-/ACG]GATTCAGGCCCCAGA	4542
rs199578955	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8563281	TATAGGCATGAGCCA[C/T]TGTGCTTGGCCACTT	4542
rs199584431	snp	C/T	0.00120375	0.0245036	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550165	CCCCACTCGCCTCCA[C/T]GAGGAAGTCGAAGAG	4542
rs199598850	in-del	-/CC/CCC	0.00035521	0.0133221	intron-variant	MYO1F	GRCh38.p7	19:8548334	GCGGTGTGGGTGGGG[-/CC/CCC]ACAGGAAGTCAGTGG	4542
rs199655160	snp	G/T	0.00217076	0.0328735	utr-variant-5-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8577313	AGGACTTACCATGGT[G/T]GGGGGCTGGTGTCTG	4542
rs199663368	snp	C/T	0.000351691	0.013256	missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536338	GAAGCAGGTGCTGGA[C/T]GCCCTGGCGTTCGTC	4542
rs199721373	snp	G/T	0.000331159	0.0128635	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554555	GCGTAGATGTGCGGG[G/T]GATTCTCATACTGGG	4542
rs199774665	in-del	-/C			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578069	AAACCAAAAAAACAA[-/C]AACAACAGGGAAGGG	4542
rs199790449	snp	C/T	9.93591e-05	0.00704767	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8551775	TTCTGTCGTCCGTGC[C/T]GTCCACCTGGTAGGT	4542
rs199804599	snp	C/T	0.000168811	0.00918568	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550182	AGGAAGTCGAAGAGG[C/T]GGGCATAGAGCCCCT	4542
rs199833314	snp	A/G	8.63237e-05	0.0065692	intron-variant	MYO1F	GRCh38.p7	19:8530580	GAGGAAAAGCTGGGC[A/G]GGGGTCGTGGGGGGC	4542
rs199843474	snp	C/T	0.000352535	0.0132719	intron-variant	MYO1F	GRCh38.p7	19:8526947	CGTGCTGGGGAGGGG[C/T]GGGTGAGAGCGTCAG	4542
rs199877698	in-del	-/TTA			intron-variant	MYO1F	GRCh38.p7	19:8570087	ATACATTTTTTTTTT[-/TTA]TTTGAGATGGAGTCT	4542
rs199886043	snp	A/G	0.00050509	0.0158836	missense	MYO1F	GRCh38.p7	19:8522488	GTGTCCGAGGCTGGG[A/G]CTTGGGTCGGCCCAC	4542
rs199886398	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8574653	TTTCTTTCCTTTCTT[C/T]CTCTTTCTTCTTTCT	4542
rs199899608	in-del	-/GGTGC	0.0490535	0.14873	intron-variant	MYO1F	GRCh38.p7	19:8552616	CAGGTGTAATACTGA[-/GGTGC]AGTCTATGAGATGGA	4542
rs199953551	snp	C/G/T	0.000366202	0.0135272	missense	MYO1F	GRCh38.p7	19:8522409	ATGACCTCGTTCACG[C/G/T]TGAAGCTCAGCTCGT	4542
rs199961022	in-del	-/C			intron-variant	MYO1F	GRCh38.p7	19:8571421	TTTCTCTCTCTCTCT[-/C]TTTTTTTTTTTTAGA	4542
rs199971487	snp	C/T	0.000224519	0.0105929	missense	MYO1F	GRCh38.p7	19:8522691	TGCTCTGAGGGCGGA[C/T]GTGCCCGGGGTCGTC	4542
rs199981303	snp	A/G	0.00369795	0.0428404	synonymous-codon, stop-gained, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536546	GGCGAAGCCGGCTCT[A/G]CGCACCCTGATGTTC	4542
rs200001876	snp	A/G	0.000116185	0.00762097	synonymous-codon, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530202	GTGCCTCACCTTGAA[A/G]CGGCGGTCGTACTTG	4542
rs200007531	snp	C/T	3.32436e-05	0.00407685	missense, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550693	ATAACCTGCATAGCA[C/T]TCTGTGGTACAACGG	4542
rs200043019	snp	C/G	0.00115852	0.0240399	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8551844	TGAGGCCCAGGTTCT[C/G]CCTTTGCTCCTGGGA	4542
rs200079933	in-del	-/TG			intron-variant	MYO1F	GRCh38.p7	19:8541404	TAATGCTATGTTCTT[-/TG]TGTGTGTGTGTGTGT	4542
rs200081850	in-del	-/TC	0.425277	0.178263	intron-variant	MYO1F	GRCh38.p7	19:8561599	CCTCCCTCCCTCTCT[-/TC]TCTTTTTTCTTTCTC	4542
rs200121209	in-del	-/TCTG	0.0166325	0.0896639	intron-variant	MYO1F	GRCh38.p7	19:8555523	GAGCCCTGCTGTCAC[-/TCTG]TCTGTCCTCTGTGTC	4542
rs200155068	snp	A/G	0.000430642	0.0146675	intron-variant	MYO1F	GRCh38.p7	19:8551910	ATGCATCTGGTGCTT[A/G]CCTGGCTCAGCCCCT	4542
rs200159025	snp	A/T	2.65961e-05	0.00364655	missense	MYO1F	GRCh38.p7	19:8522772	CCCCCTCCAGACATG[A/T]TCTCCAGGGGCAGGG	4542
rs200184077	in-del	-/TGC			intron-variant	MYO1F	GRCh38.p7	19:8543645	GGAACACGGTGGTGG[-/TGC]TGGTGGTGCTGGTGG	4542
rs200190836	snp	C/T	0.02016	0.0983543	intron-variant	MYO1F	GRCh38.p7	19:8522223	GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG	4542
rs200194968	snp	C/T	0.00120879	0.0245547	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544402	TGTCTGGTCTGCTCC[C/T]CCGCCCGTGGCGTGC	4542
rs200197098	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8533354	CTTCTTCTTCTTCTT[C/T]TTCTTTTTTTTTTTT	4542
rs200225777	snp	C/T	0.000216405	0.0103998	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8527351	ACCTGAGGGAGACTC[C/T]CCGCAGAGCCTGGAT	4542
rs200229672	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8548592	CTGCACCTCTATTTT[C/T]TTTTTTTTTTTTTCT	4542
rs200260054	in-del	-/CTG			intron-variant	MYO1F	GRCh38.p7	19:8543978	GTGGTGGTGCTGGTG[-/CTG]GTGCTGGTGGTGGTG	4542
rs200264775	snp	A/G	0.000662295	0.0181854	intron-variant	MYO1F	GRCh38.p7	19:8553467	AGGAATAAATGATCA[A/G]TGGTTGGGGAAGAGC	4542
rs200305208	in-del	-/CC	0.123798	0.215808	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578061	AACAAAAAAACCAAA[-/CC]AAAACAACAACAACA	4542
rs200309964	in-del	-/TGC			intron-variant	MYO1F	GRCh38.p7	19:8543738	TGCTGGTGGTGCTGG[-/TGC]TGGTGCTGGTGGTGG	4542
rs200334457	in-del	-/TGAA	0.0126979	0.078662	intron-variant	MYO1F	GRCh38.p7	19:8569099	TCAATACATACTTGT[-/TGAA]TGAATGAATGAATGA	4542
rs200369684	snp	A/C/T	0.000797844	0.0199573	synonymous-codon, missense	MYO1F	GRCh38.p7	19:8525561	TCCCTTCCGCGTAGG[A/C/T]TCTGAAAGAAGAGTG	4542
rs200375822	snp	A/C/T	0.000415227	0.014403	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8530494	TACTTCCGGACAGCC[A/C/T]CGTGGCGCCGCCAGG	4542
rs200383611	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8532885	AGAGTGAGATCCTGT[C/T]TCAGAAAAAAAAAAA	4542
rs200391716	snp	C/G	0.000183316	0.00957205	intron-variant	MYO1F	GRCh38.p7	19:8537077	CAGAAGTGAAGACGG[C/G]TGGGTGGGGGGCACA	4542
rs200396679	snp	C/G/T	1.65603e-05	0.00287747	synonymous-codon, missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554545	GTCCGTGAGGGCGTA[C/G/T]ATGTGCGGGGGATTC	4542
rs200408762	snp	C/T	0.00160571	0.0282891	intron-variant	MYO1F	GRCh38.p7	19:8551711	TGAGGTCTGCCTGGC[C/T]GGGGACTGGAGTAGA	4542
rs200467110	snp	C/T	0.00739325	0.0603487	intron-variant	MYO1F	GRCh38.p7	19:8547988	TCATGGTCCTTCCAC[C/T]CCACCCCCACCCCAG	4542
rs200484581	in-del	-/TTTTTCTTTTCTT	0.0314385	0.121371	intron-variant	MYO1F	GRCh38.p7	19:8558159	CTCTCTCAGTTTTTC[-/TTTTTCTTTTCTT]TTTTTCTTTTGAGTC	4542
rs200488055	snp	A/G	0.000115679	0.00760433	intron-variant	MYO1F	GRCh38.p7	19:8553343	CCTTCTGTTTTCCTC[A/G]TCTCACCTGGACCTT	4542
rs200512178	in-del	-/CCTTCCTTTCTCCTCTCCCTC			intron-variant	MYO1F	GRCh38.p7	19:8561397	CCCCCTTCTTTCCTT[-/CCTTCCTTTCTCCTCTCCCTC]CCTTCCTTTCTCCTC	4542
rs200542253	snp	A/G	0.000117464	0.0076628	intron-variant	MYO1F	GRCh38.p7	19:8526939	TCCTGTCGCGTGCTG[A/G]GGAGGGGCGGGTGAG	4542
rs200548397	snp	A/G	0.000119696	0.00773522	synonymous-codon	MYO1F	GRCh38.p7	19:8522471	CCGGCACCTGGGACC[A/G]TGTGTCCGAGGCTGG	4542
rs200593021	snp	A/C/G	4.97165e-05	0.0049856	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550638	CAAGATCCCCGCCAC[A/C/G]AGCTGCAGGACCAGC	4542
rs200628309	in-del	-/T	0.0236746	0.106192	intron-variant	MYO1F	GRCh38.p7	19:8548959	GCTTTTTCTTTTCTA[-/T]TTTTTTTTGAGATGG	4542
rs200635354	snp	C/T	0.000496689	0.0157511	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554533	CCGGTACATGTTGTC[C/T]GTGAGGGCGTAGATG	4542
rs200722509	in-del	-/CAG	0.0146672	0.084371	intron-variant	MYO1F	GRCh38.p7	19:8531489	GAGTAGCTGGGACTA[-/CAG]CTGTGAGCCACCATG	4542
rs200726649	snp	C/T	1.6577e-05	0.00287893	missense, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530231	TGGTGACCGAATCGG[C/T]GAAGTCCACCCGCTC	4542
rs200733671	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8534061	GCGGGTGCCTGTAAT[C/T]CCAGCTACTTGGGAG	4542
rs200744759	snp	C/G/T	0.00187691	0.030577	synonymous-codon, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536366	GTCCCCACGCCACCG[C/G/T]GGCCACGTCTCGGGG	4542
rs200746623	snp	C/T	0.00074494	0.0192851	synonymous-codon, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8545680	GAGGTCACAGACGAC[C/T]TTGTTGTTGAAGTAC	4542
rs200787792	snp	A/T			intron-variant	MYO1F	GRCh38.p7	19:8523034	TTAAAATTATTTTTT[A/T]CTTTTTTTTTTTTTT	4542
rs200794296	snp	C/T	0.000747977	0.0193243	intron-variant	MYO1F	GRCh38.p7	19:8540076	GTATGGCTAGACTTT[C/T]GGGTACTCTTCCTCC	4542
rs200797032	snp	C/T	0.000993358	0.0222641	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544317	CAGCGTAGTGGTGGA[C/T]GACGAAGCCGGCGCT	4542
rs200807245	in-del	-/AAAC			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578053	CCAGAAAAAACAAAA[-/AAAC]AAACCAAAAAAACAA	4542
rs200858073	snp	C/T	0.000332515	0.0128898	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8537043	GTGTGGCCACCAGGT[C/T]GTTGGCTTGTTTCTG	4542
rs200864651	snp	C/T	0.00410117	0.0450973	missense	MYO1F	GRCh38.p7	19:8522517	ACACCAGGCACTGGC[C/T]GTTGCCCCACGCTGC	4542
rs200871128	snp	C/G	3.42618e-05	0.00413881	missense	MYO1F	GRCh38.p7	19:8525547	TTTCCCTTGGCCATT[C/G]CCTTCCGCGTAGGCT	4542
rs200885736	in-del	-/C	0.141258	0.225111	intron-variant	MYO1F	GRCh38.p7	19:8571422	TCTCTCTCTCTCTCT[-/C]TTTTTTTTTTTAGAT	4542
rs200910214	snp	C/T	0.000389012	0.0139411	utr-variant-3-prime	MYO1F	GRCh38.p7	19:8521493	CGGCAGGCAGATAGG[C/T]GGGCGAAAGAGAAGG	4542
rs200911217	snp	C/T	3.34863e-05	0.0040917	missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536322	TCCATGTTGACCGCC[C/T]GAAGCAGGTGCTGGA	4542
rs200924489	in-del	-/GA			downstream-variant-500B	MYO1F	GRCh38.p7	19:8520529	GATCTCCTGACCTTG[-/GA]TGATCTGCCCGCCTC	4542
rs200935728	snp	C/T	0.000116041	0.00761624	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530178	GGGTCTTGCTGTGCC[C/T]ACCCACTAGTGCCTC	4542
rs200968078	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8574654	TTCTTTCCTTTCTTT[C/T]TCTTTCTTCTTTCTC	4542
rs201007272	snp	C/T	0.000131771	0.00811592	synonymous-codon	MYO1F	GRCh38.p7	19:8522729	TCCCAGGGATGTGGA[C/T]GGAGGGCCCCGGGGA	4542
rs201056652	snp	C/T	0.000986942	0.0221923	intron-variant	MYO1F	GRCh38.p7	19:8522629	TGCCCTCCCACCCCA[C/T]CTACCCGGCCATGCC	4542
rs201068411	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8543762	GTGGTGGTGGTGGTG[G/T]TGGTGCTGGTGGTGC	4542
rs201111806	in-del	-/C			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578072	CCAAAAAAACAACAA[-/C]AACAGGGAAGGGTGC	4542
rs201115094	snp	A/G	0.000480152	0.0154869	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8551767	AAAGTCGCTTCTGTC[A/G]TCCGTGCCGTCCACC	4542
rs201138222	snp	A/G	3.34907e-05	0.00409197	missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536319	GGCTCCATGTTGACC[A/G]CCCGAAGCAGGTGCT	4542
rs201164800	snp	A/G	5.08582e-05	0.00504247	intron-variant	MYO1F	GRCh38.p7	19:8544260	GCCCTGGGGGTCTGC[A/G]AGGAGGCACAGGGTA	4542
rs201176156	in-del	-/TGC			intron-variant	MYO1F	GRCh38.p7	19:8543789	TGCTGGTGGTGCTGG[-/TGC]TGGTGGTGGTGCTGG	4542
rs201191520	snp	A/G	0.000248425	0.0111423	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554655	AGCCCCAGCCTCACC[A/G]CGCCCTGATAGAGGT	4542
rs201198914	snp	A/C/G	0.00031083	0.0124628	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8527474	TCAGGATCAAGTCCC[A/C/G]CTTGATGGGCTGTGG	4542
rs201226019	in-del	-/GGCCGC			intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526683	TTGGGGCAGGGGCGG[-/GGCCGC]GGCCGGGGCCGAAGC	4542
rs201239697	in-del	-/TCTTTTTCTTTCTC			intron-variant	MYO1F	GRCh38.p7	19:8574708	CTTTCTCTCTTTCTT[-/TCTTTTTCTTTCTC]TTTCTTTCTTTCTTT	4542
rs201247952	snp	C/T	0.0952156	0.196321	intron-variant	MYO1F	GRCh38.p7	19:8561396	CCCCCCTTCTTTCCT[C/T]CCTTCCTTTCTCCTC	4542
rs201259088	in-del	-/AGTC	0.0166325	0.0896639	intron-variant	MYO1F	GRCh38.p7	19:8563016	TTTGTTTTGATACCG[-/AGTC]AGTCTCACTCTGTCG	4542
rs201288038	in-del	-/GGC			intron-variant	MYO1F	GRCh38.p7	19:8543649	CACGGTGGTGGTGGT[-/GGC]GGTGCTGGTGGTGGT	4542
rs201305709	snp	C/T	3.32033e-05	0.00407438	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8530485	ATCTCCTCGTACTTC[C/T]GGACAGCCACGTGGC	4542
rs201325015	snp	A/G	8.34133e-05	0.00645753	synonymous-codon, missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536534	CTGGCGGCGGTAGGC[A/G]AAGCCGGCTCTGCGC	4542
rs201331083	snp	A/G	0.00052117	0.0161342	synonymous-codon, stop-gained, nc-transcript-variant	MYO1F	GRCh38.p7	19:8540004	TCCATCCAGCTTCTC[A/G]GGGAAGAGCATCCGG	4542
rs201336903	in-del	-/G/GTT/TT	0.365232	0.22186	intron-variant	MYO1F	GRCh38.p7	19:8541426	TGTGTGTGTGTGTGT[-/G/GTT/TT]TTTTTTTTTTTTTTT	4542
rs201353639	snp	C/T	3.31307e-05	0.00406992	splice-donor-variant	MYO1F	GRCh38.p7	19:8555658	CCTTGGCCCAGGGTA[C/T]GAAGATGTAGTCGTC	4542
rs201360664	in-del	-/G	0.0490535	0.14873	intron-variant	MYO1F	GRCh38.p7	19:8552617	AGGTGTAATACTGAA[-/G]GTCTATGAGATGGAT	4542
rs201364078	snp	C/G/T	0.000363642	0.0134795	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8553361	TCACCTGGACCTTCT[C/G/T]GCCTCCGCCAGACAC	4542
rs201381925	in-del	-/TGC			intron-variant	MYO1F	GRCh38.p7	19:8544053	TGCTGGTGGTGGTGG[-/TGC]TGGTGGTGGTGGTGG	4542
rs201470925	in-del	-/C			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578066	AAAAAACCAAAAAAA[-/C]AACAACAACAGGGAA	4542
rs201472367	snp	A/G	3.3123e-05	0.00406945	intron-variant	MYO1F	GRCh38.p7	19:8548127	AAGCCATTTTTCTGC[A/G]GAAGGAGGAAAAGGG	4542
rs201477859	in-del	-/CTT			intron-variant	MYO1F	GRCh38.p7	19:8574651	CTTTCTTTCCTTTCT[-/CTT]TTCTCTTTCTTCTTT	4542
rs201524718	in-del	-/CT/TC			intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526350	TCTCTCTCTCTCTCT[-/CT/TC]GTAGACACTCCCCTT	4542
rs201538800	in-del	-/T	0.192715	0.243348	intron-variant	MYO1F	GRCh38.p7	19:8556006	CCTCTATTTTTTTTT[-/T]AATTTTTAATTTTTA	4542
rs201539438	snp	A/G	4.96792e-05	0.00498368	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554506	CTGGTTCTCACAGTC[A/G]ATAAGCATGTTCCGG	4542
rs201578688	snp	A/C/G	0.00636408	0.0560503	intron-variant	MYO1F	GRCh38.p7	19:8522599	CTCCCCTACCCCCTG[A/C/G]CCACCTCCTGGAGCT	4542
rs201600416	in-del	-/ACTT	0.0532157	0.154195	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8536048	GTCTATTAATCTCTC[-/ACTT]GCTTTCTCAATTTCT	4542
rs201618281	snp	C/G	0.000302658	0.0122979	missense	MYO1F	GRCh38.p7	19:8525484	AGCTCCTCACCTCTG[C/G]GGGGCGCAGGGGCCG	4542
rs201640620	snp	C/G	0.000201032	0.0100238	missense	MYO1F	GRCh38.p7	19:8522444	ATCTTGGCCCACGTA[C/G]TGGTATAGGGCCCGG	4542
rs201642007	snp	A/G	0.000148695	0.00862122	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8553166	ATTGTTGTTGCGCAC[A/G]GTCTTGGCGTTGCCG	4542
rs201645601	snp	C/T	0.000202974	0.010072	missense	MYO1F	GRCh38.p7	19:8525535	GACCTCCGAGGTTTT[C/T]CCTTGGCCATTCCCT	4542
rs201646155	snp	C/T	0.000251385	0.0112084	missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536350	GGACGCCCTGGCGTT[C/T]GTCCCCACGCCACCG	4542
rs201654775	snp	A/G	0.000976619	0.0220761	missense, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8545712	GGATTGGAGTCCAGC[A/G]GATGCCTTCCTGCAC	4542
rs201662136	in-del	-/CCTTCCTTCCTTTCTCCTCTC			intron-variant	MYO1F	GRCh38.p7	19:8561393	CTTCCCCCCTTCTTT[-/CCTTCCTTCCTTTCTCCTCTC]CCTCCCTTCCTTTCT	4542
rs201712602	snp	A/G	3.34359e-05	0.00408862	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550215	GCCAGGGCATCACGG[A/G]TGTAGGCTGCCTGCT	4542
rs201718326	snp	A/G	3.38799e-05	0.00411568	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8526851	GCGCTTGCACAGAAG[A/G]CTGACAAACTCGGTC	4542
rs201723456	snp	C/T	8.4241e-05	0.00648949	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8527431	TTCTTCACTTTCTCT[C/T]GCCCAATCACATACA	4542
rs201794765	snp	C/T	0.000155981	0.00882983	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544408	GTCTGCTCCCCCGCC[C/T]GTGGCGTGCATGGTG	4542
rs201807711	snp	C/T	0.0368353	0.130617	intron-variant	MYO1F	GRCh38.p7	19:8561472	TCCCTCTCTCTCTCT[C/T]TCTTTTTCTCTTTCT	4542
rs201832487	snp	A/C/T	0.00803974	0.0628938	missense	MYO1F	GRCh38.p7	19:8522824	GCACCCCATTGCGAT[A/C/T]CATGCCTGTGGCAGG	4542
rs201869595	snp	A/G	1.68513e-05	0.00290265	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544306	GCGCACCTTGCCAGC[A/G]TAGTGGTGGATGACG	4542
rs201876554	snp	C/T	0.00165467	0.0287158	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8551821	GTAGTAATAGTAGTC[C/T]GGTGTCATGAGGCCC	4542
rs201910417	snp	A/G	1.65608e-05	0.00287752	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8551758	AGTCTCACCAAAGTC[A/G]CTTCTGTCGTCCGTG	4542
rs201922845	snp	A/C/G	1.65616e-05	0.00287759	intron-variant	MYO1F	GRCh38.p7	19:8554461	AGGGTCTGTGGCCCC[A/C/G]CAACTCTGTCCATAC	4542
rs201962739	snp	C/T	0.00248603	0.0351687	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550668	CTGCTGGATGCTGGG[C/T]GGGATCCCAATAACC	4542
rs201979058	snp	C/T	0.000150425	0.00867121	intron-variant	MYO1F	GRCh38.p7	19:8548029	CCCTGACTGCTTGGC[C/T]GCCCACCTGCTCGGC	4542
rs201982814	snp	C/T	0.00146414	0.0270172	missense	MYO1F	GRCh38.p7	19:8522527	CTGGCCGTTGCCCCA[C/T]GCTGCGCTTCCTCTG	4542
rs201988076	snp	C/T	0.00011602	0.00761554	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530433	CTTGTGCCCCCACCC[C/T]GCGCCGTTTACCCGA	4542
rs202022482	in-del	-/TGC			intron-variant	MYO1F	GRCh38.p7	19:8543729	TGGTGGTGGTGCTGG[-/TGC]TGGTGCTGGTGGTGC	4542
rs202056749	snp	C/T	0.00159427	0.0281885	intron-variant	MYO1F	GRCh38.p7	19:8539933	CAGCTCCCCGTTGTA[C/T]ACCCCAGGCCCACCT	4542
rs202070013	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8571148	GAAGACAGCAAACAA[A/C]CAGCCACTTCCTTCC	4542
rs202089713	in-del	-/TA	0.0494327	0.149241	intron-variant	MYO1F	GRCh38.p7	19:8552613	GTGCAGGTGTAATAC[-/TA]TGAAGTCTATGAGAT	4542
rs202093600	in-del	-/GGT			intron-variant	MYO1F	GRCh38.p7	19:8543968	GGTGGTGGTGGTGGT[-/GGT]GCTGGTGCTGGTGCT	4542
rs202149252	snp	C/G/T	0.0003482	0.0131905	intron-variant	MYO1F	GRCh38.p7	19:8553482	GTGGTTGGGGAAGAG[C/G/T]CCTTTTTAGTGCCTG	4542
rs202192712	in-del	-/C	0.0441095	0.141807	intron-variant	MYO1F	GRCh38.p7	19:8539536	AGGAGGCGGAGGTTG[-/C]AGAGGGCCCAGATTG	4542
rs202193577	in-del	-/C	0.123798	0.215808	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578057	GAAAAAACAAAAAAA[-/C]CAAAAAAACAACAAC	4542
rs202195089	snp	A/G	0.00199795	0.0315433	missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536373	CGCCACCGCGGCCAC[A/G]TCTCGGGGGTCAGAA	4542
rs202232245	snp	C/T	0.000503854	0.0158642	intron-variant	MYO1F	GRCh38.p7	19:8536902	AGTTCTAGGGGTAAC[C/T]GCAGGGCCTGGGGGG	4542
rs367561429	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8542170	AGAATAGGGGATGGG[G/T]GGCGGGCTTCCTGGA	4542
rs367568601	snp	C/T	6.68527e-05	0.00578117	missense	MYO1F	GRCh38.p7	19:8521580	TCCTGGCCGTGAAGC[C/T]GGCCCTTCCACCAGC	4542
rs367585526	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8528506	GCACTCCAGCCTGGG[C/T]GACATAACAAGATTC	4542
rs367608654	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8533328	GCCAGCGTGCCCAGC[C/G]TCAGATTCTTCTTCT	4542
rs367664156	snp	A/G	0.0003314	0.0128682	intron-variant	MYO1F	GRCh38.p7	19:8545778	GGGGCCAGTGAAAAA[A/G]TTGTGGCCACCCTTC	4542
rs367667498	snp	C/G	0.000319949	0.012644	missense, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526551	CGGGAGAAGGTGACG[C/G]TGCGGGTGCCGCCAC	4542
rs367686773	snp	C/T	8.39313e-05	0.00647755	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8539961	CCTTGATCTTGGAGC[C/T]GGCGGTGCTGGGGCG	4542
rs367691596	snp	C/T	0.000315026	0.0125465	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530456	TTACCCGAAGCCTCT[C/T]ACCTTCCTCCCGCAT	4542
rs367713395	snp	A/G	3.34818e-05	0.00409143	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8527410	ACCTGGCCCTTCTCA[A/G]GTCCCTTCTTCACTT	4542
rs367720693	snp	A/G	1.70223e-05	0.00291734	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544367	TGGGTCCCCACAGCC[A/G]CCTGCAGCTTCTGCA	4542
rs367762414	snp	A/G	0.000159987	0.00894248	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8536445	ATAGCAGACAGGCCT[A/G]GCTGGGCGTTCTGAT	4542
rs367763769	in-del	-/C			intron-variant	MYO1F	GRCh38.p7	19:8563796	GATTACAGGGGTGAG[-/C]CCACCGCGCCTGGCT	4542
rs367779182	in-del	-/T			intron-variant	MYO1F	GRCh38.p7	19:8563515	TTCTTTCTTTCTTTC[-/T]TTTTTTTTTTGAGAT	4542
rs367779407	snp	C/T	3.94244e-05	0.00443967	intron-variant	MYO1F	GRCh38.p7	19:8522620	TCCTGGAGCTGCCCT[C/T]CCACCCCACCTACCC	4542
rs367801862	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8565387	GTCTCCACTAAAAGT[A/G]CAACATTAGCCAGGT	4542
rs367814925	snp	A/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8551478	TGCCTCTGCCTCCCC[A/G]GTAGCTGGGATTACA	4542
rs367816917	snp	A/C	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8553193	GCCGAAGGCCTCGAG[A/C]AGCGGGTTGGACTGC	4542
rs367839664	snp	C/T	0.00358779	0.0422022	intron-variant	MYO1F	GRCh38.p7	19:8525270	GAGGAGAGAAGATGT[C/T]AGTGGTTAGCTGGGT	4542
rs367878445	in-del	-/G			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8577499	GCCGAGGCCATGGGG[-/G]AGGGAAGCTGGGTGT	4542
rs367916306	snp	A/G	0.000231903	0.0107656	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554684	GTCGATCTCACGGTC[A/G]GTGAAGTAGGGCATC	4542
rs367924210	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8559676	TTAACACGACCGGGC[A/G]CGGTGGCTCACACCT	4542
rs367926533	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8544666	GGGATAGGGGGGCAA[C/G]GGTGTGTGGGGCTAC	4542
rs367942797	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8522313	AGGCGTGAGCCACCG[C/T]GCCCGGCCGATGTCA	4542
rs367956320	in-del	-/AAAGAAAG			intron-variant	MYO1F	GRCh38.p7	19:8556483	CCCGTCTCTATAAAA[-/AAAGAAAG]AAAGAAAGAAAGAAA	4542
rs367972611	snp	A/G	4.96833e-05	0.00498389	intron-variant	MYO1F	GRCh38.p7	19:8545627	CAGTGAGACGCCCCC[A/G]CCAAAGTTGACCCAG	4542
rs367972902	in-del	-/T			intron-variant	MYO1F	GRCh38.p7	19:8552266	CTCTTCCCTTCTTCC[-/T]TTTTTTTTTTGAGAC	4542
rs368071444	in-del	-/T	0.00597247	0.0543191	intron-variant	MYO1F	GRCh38.p7	19:8572607	TTTCTCCTAAATTCC[-/T]TTTGACTCCCAGCCT	4542
rs368125243	snp	C/T	1.66299e-05	0.00288352	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8530510	CGTGGCGCCGCCAGG[C/T]CTTCTGGATGGTTCG	4542
rs368127869	snp	C/T	0.000780403	0.0197381	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526605	CGAAACTGTAGTCTA[C/T]GGGGAGAGAAGAAAG	4542
rs368210279	snp	A/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8564441	GAGTCCCTGGGGTGC[A/G]TCAGGAGATGACAGA	4542
rs368326573	snp	A/G	8.65913e-05	0.00657937	synonymous-codon, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526493	CACGCTGACCGTGAG[A/G]GTCCGACCGCCAACC	4542
rs368363753	snp	C/T	6.95689e-05	0.00589742	intron-variant	MYO1F	GRCh38.p7	19:8555834	GGGTGAGCCCTTGCA[C/T]GGGGATGCGGCACCT	4542
rs368370926	snp	G/T	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8542426	CAGGGGCCAGTGCAG[G/T]GGGCCTGTGTCAGGA	4542
rs368388019	snp	C/G/T	3.31209e-05	0.00406935	intron-variant	MYO1F	GRCh38.p7	19:8548159	CCTTCCCTCAATGTC[C/G/T]TGGTGCTGGAAGTTC	4542
rs368435303	snp	A/G	9.19633e-05	0.00678035	synonymous-codon	MYO1F	GRCh38.p7	19:8522636	CCACCCCACCTACCC[A/G]GCCATGCCCTGGTCA	4542
rs368465180	snp	C/T	1.82854e-05	0.00302363	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550314	AGCTTCTCCTGCAGT[C/T]GCCCGCTGTCAATGC	4542
rs368498641	snp	C/T	6.661e-05	0.00577067	intron-variant	MYO1F	GRCh38.p7	19:8554763	GGGATGGTTAAGGGT[C/T]GTGTGGTGTCCTGGT	4542
rs368566087	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8554575	CTCATACTGGGCCTG[A/G]CAGGGGAGGTCAGGT	4542
rs368580324	snp	A/G/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8574481	CATGGACCATGGAGC[A/G/T]GGGCATTAGATTTTC	4542
rs368586862	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8559084	GGGGTTTCACTGTGT[C/T]GCTCAGGCTGGTCTT	4542
rs368617557	snp	A/G	0.000207236	0.0101772	missense	MYO1F	GRCh38.p7	19:8522688	TTGTGCTCTGAGGGC[A/G]GACGTGCCCGGGGTC	4542
rs368622600	snp	A/G	1.67156e-05	0.00289093	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8536479	GGGGATGGCGAGGGC[A/G]GGGGTGGAGGGCTCC	4542
rs368629918	snp	A/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8553542	GCCTGCCAGTATTCC[A/G]GGTACTGGGGATACT	4542
rs368634902	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8522932	GAGGAGACTGCGACA[C/T]TCTCAACCCAGTGTG	4542
rs368636425	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8537411	CCTTTGGGGAGATAG[C/G]TACCTTGGGTGTTTG	4542
rs368638726	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8561976	CATGTCGGCCTCCCA[A/G]AGTGCTGGGATTACA	4542
rs368696066	snp	A/C	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8564557	AAAACCCGGACCAGG[A/C]AGGGGAGGCCCAGAT	4542
rs368710019	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8570794	ATTACAGGTGCAAGC[C/T]GCTGTGCCCGGCCAA	4542
rs368749334	snp	C/T	0.000165634	0.00909888	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8548272	AAATGTCCAGCACAC[C/T]GATGCTGTACTCTTC	4542
rs368755221	snp	C/G	0.00398564	0.0444627	intron-variant	MYO1F	GRCh38.p7	19:8527247	CATGGCACCAGGTAA[C/G]ATTGTCAGGGTAACA	4542
rs368777838	in-del	-/C/CCAA			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578060	AAACAAAAAAACCAA[-/C/CCAA]AAAAACAACAACAAC	4542
rs368786181	snp	C/T	6.72755e-05	0.00579942	synonymous-codon	MYO1F	GRCh38.p7	19:8522450	GCCCACGTACTGGTA[C/T]AGGGCCCGGCACCTG	4542
rs368793623	snp	A/C/T	6.66249e-05	0.00577136	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8527374	GCCTGGATGTCCACT[A/C/T]TCTTCTTCAAGACTT	4542
rs368817158	snp	C/T	9.93986e-05	0.00704907	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550579	TCCACACTCTCCACT[C/T]GGGCGTAATTCCCGT	4542
rs368817578	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8562290	ATAGGCATGAGCCAC[C/T]GCACCGGCCCTTCCT	4542
rs368818036	snp	A/G			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578823	GGGGGACCCATGTTC[A/G]GATCTATCTTTGGTC	4542
rs368832750	snp	A/G	0.00140849	0.0265002	utr-variant-5-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8577363	ATGGGTCGTGATGGA[A/G]GTGCAGGTTCAGGGG	4542
rs368834940	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8528081	ACAAAAATTAGCTGG[A/G]CGAGGTGGTGGGCAC	4542
rs368868905	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8533783	GAGTTTGTGGAACTT[C/T]GTTTCAGCTGTCCCA	4542
rs368903014	snp	C/T	0.000181832	0.00953325	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8553367	GGACCTTCTCGCCTC[C/T]GCCAGACACCTTGGA	4542
rs368903586	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8537140	CCCTGGATACAGTCC[C/T]AATAGACAGAGACTG	4542
rs368908985	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8552699	TTGCATAGATTTTTT[C/T]CCCCCCCAGGCTACA	4542
rs368914147	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8556422	TGAGGCAGGAGGATC[A/G]CTTGAGGCCAGGAGT	4542
rs368926502	snp	A/G	3.35272e-05	0.0040942	stop-gained, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8541955	AGAAGAGAACGTCTC[A/G]GTTCCTCTCGCAGAA	4542
rs368938645	snp	C/T	1.67038e-05	0.00288992	intron-variant	MYO1F	GRCh38.p7	19:8554778	CGTGTGGTGTCCTGG[C/T]AGGTTTTGTCCTCCC	4542
rs368939767	snp	C/T	0.000168515	0.00917763	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544320	CGTAGTGGTGGATGA[C/T]GAAGCCGGCGCTCCA	4542
rs368987048	in-del	-/TTT			intron-variant	MYO1F	GRCh38.p7	19:8545282	TTAGTAGAGACAGGT[-/TTT]CACCATATTGGTCAG	4542
rs368997430	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8568310	CGCCCGTAGTCCCAG[C/T]TCCTCGGGAGGCTGA	4542
rs369074813	snp	C/T			intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8529802	TGCTATACTTGAGTG[C/T]ATACCTGTGGGCAGG	4542
rs369077601	in-del	-/TC			intron-variant	MYO1F	GRCh38.p7	19:8574578	CTTTCTTTCTTTCTT[-/TC]TCTCTCTCTCTCTCT	4542
rs369079847	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8574903	TGGGGTTACAGGCGC[A/G]CACCACCACGACTGG	4542
rs369094611	in-del	-/T			intron-variant	MYO1F	GRCh38.p7	19:8562164	CCGGCTAATTTTTTC[-/T]TTTTTTTTTTGTATT	4542
rs369101949	snp	C/G	1.6795e-05	0.0028978	missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536257	ACACACTCACCGACT[C/G]TGGGTTCTTGACAAA	4542
rs369105985	snp	C/T	8.28288e-05	0.00643487	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555712	CGGCAATGGCGTCTT[C/T]GGTGATCTGGGGAAG	4542
rs369108938	snp	A/C/T	0.00284511	0.0376098	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8552136	TCTGGCTCCCCACCT[A/C/T]GGCTGAACTGGATCT	4542
rs369110462	snp	C/T	6.73106e-05	0.00580093	intron-variant	MYO1F	GRCh38.p7	19:8548354	GAAGTCAGTGGGCAT[C/T]GGTCAGATCTGAAGC	4542
rs369112367	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8559991	AGAATTAACACTCAG[C/T]GAGCACCTATGCTGT	4542
rs369113604	snp	A/C	8.28041e-05	0.00643391	intron-variant	MYO1F	GRCh38.p7	19:8545622	GGGACCAGTGAGACG[A/C]CCCCGCCAAAGTTGA	4542
rs369185608	snp	C/T	0.000163987	0.00905354	intron-variant	MYO1F	GRCh38.p7	19:8552010	CAGGTGGTGCTCCCT[C/T]TCCCCCGGCCCCTTC	4542
rs369189498	snp	A/C	5.06222e-05	0.00503076	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8526858	CACAGAAGGCTGACA[A/C]ACTCGGTCTTGAAGA	4542
rs369203052	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8545577	CATAACACCCTTGGC[A/C]CTCCCCCTCATCTTC	4542
rs369249121	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8523132	CGCCTCCTGGGTTCA[C/T]GCCATTCTCCTGCCT	4542
rs369264348	in-del	-/C			intron-variant	MYO1F	GRCh38.p7	19:8574238	AAACAGCCACAACCA[-/C]CCACCACAACCAATG	4542
rs369289030	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8564697	ATAGACAGGAATGAG[A/G]ATCTGGCTGAGAAGG	4542
rs369292088	snp	G/T	0.000314635	0.0125387	intron-variant	MYO1F	GRCh38.p7	19:8554449	GGCCCGGGCAGCAGG[G/T]TCTGTGGCCCCCCAA	4542
rs369340970	snp	A/G	0.000159987	0.00894248	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555779	GTGGCTCTGCCAGTG[A/G]AAGCGCTCCTTGCTG	4542
rs369342617	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8529337	CCAGGTACAGGTGAC[A/G]GTAAACAGGCCAAGT	4542
rs369349036	snp	C/T			missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8553433	TCCCAGCTCCACTCT[C/T]TCCACTGGGGATGAA	4542
rs369359209	snp	C/T	6.72585e-05	0.00579868	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8540003	CTCCATCCAGCTTCT[C/T]GGGGAAGAGCATCCG	4542
rs369361765	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8532314	TTTGAGTTGTAAAAG[G/T]CTAGACCCAGAGGGG	4542
rs369499841	snp	A/T			intron-variant	MYO1F	GRCh38.p7	19:8553902	CACACACACTCTCTC[A/T]CTCTCTCTCTCTCTC	4542
rs369501756	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8555426	AAACAGGGTTGGATC[C/T]GGAATGGGGGAAATG	4542
rs369537745	snp	C/T	0.000157987	0.00888643	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536956	GGGATCACCTGTTCT[C/T]CTCCCAGTCTCGGGG	4542
rs369571817	snp	C/G	3.35458e-05	0.00409534	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8526893	CTCCAGGAAGCTGTC[C/G]GCGGCATCCTCTTGG	4542
rs369644060	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8523073	GTCTTGCTCAGTCGC[C/T]CAGGCTGGAGTGCAG	4542
rs369654315	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8525072	GGGCGTGGTGGCGGG[C/T]GCCTGTAATCTCAGC	4542
rs369682909	snp	A/T	0.0221141	0.102801	intron-variant	MYO1F	GRCh38.p7	19:8556882	ACAAGAGTGAAACTC[A/T]GTCTCAAAAAAAAAA	4542
rs369687368	in-del	CCC/G			intron-variant	MYO1F	GRCh38.p7	19:8548334	TGCGGTGTGGGTGGG[CCC/G]ACAGGAAGTCAGTGG	4542
rs369696575	in-del	-/AGAAAGAAAGAAAG			intron-variant	MYO1F	GRCh38.p7	19:8556496	AAAAGAAAGAAAGAA[-/AGAAAGAAAGAAAG]AGAAAGAAAGAGAAA	4542
rs369705937	in-del	-/TGTGAC			intron-variant	MYO1F	GRCh38.p7	19:8538974	TTAATACCACTGAAC[-/TGTGAC]ATTAAAACTGGTTAA	4542
rs369709402	snp	C/T	0.000690753	0.0185715	intron-variant	MYO1F	GRCh38.p7	19:8525430	GTCTGGCTTAGGCCA[C/T]GGGACCCACAACAGA	4542
rs369754381	snp	A/G	0.000165986	0.00910854	synonymous-codon	MYO1F	GRCh38.p7	19:8525486	CTCCTCACCTCTGGG[A/G]GGCGCAGGGGCCGCC	4542
rs369774141	snp	A/G	0.00517822	0.0506191	intron-variant	MYO1F	GRCh38.p7	19:8564142	TCCCAGCACTTTGGG[A/G]GGCCAAGGTGGATGG	4542
rs369784147	snp	C/T	0.000155988	0.00883004	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530184	TGCTGTGCCCACCCA[C/T]TAGTGCCTCACCTTG	4542
rs369803271	snp	C/T	3.31268e-05	0.00406968	intron-variant	MYO1F	GRCh38.p7	19:8554436	ATGTTTCAGCAGGGG[C/T]CCGGGCAGCAGGGTC	4542
rs369830308	snp	C/T			downstream-variant-500B	MYO1F	GRCh38.p7	19:8520544	GTGATCTGCCCGCCT[C/T]GGCCTCCCAAAGTGC	4542
rs369863077	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8563465	ACCACGCCCAGCTAA[C/T]GTTTTGTAATTTTAG	4542
rs369880513	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8556154	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC	4542
rs369882423	snp	A/C/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8568664	TGGTGGCTCACGCCT[A/C/G]TAATCCCAGCACTTT	4542
rs369884531	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8555431	GGGTTGGATCCGGAA[G/T]GGGGGAAATGGAACA	4542
rs369892335	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8576055	AGGCTGGAGTGCAGC[A/G]GCAGGATCTCAGCTC	4542
rs369910650	snp	A/T			intron-variant	MYO1F	GRCh38.p7	19:8553908	CACTCTCTCTCTCTC[A/T]CTCTCTCTCTCTCTC	4542
rs369911550	snp	A/G	1.65954e-05	0.00288053	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555761	GCCGCTCTGCTTCAC[A/G]TTGTGGCTCTGCCAG	4542
rs369961523	snp	A/C/G	0.000164234	0.00906061	intron-variant	MYO1F	GRCh38.p7	19:8544474	GGGGCTCTGCGGGGC[A/C/G]AGCGGGAGCCAGCAG	4542
rs369963846	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8550046	CTCAAAGAATGCTCC[A/C]AACTCAGCCACCCAA	4542
rs370015943	snp	C/G	0.0023933	0.0345097	intron-variant	MYO1F	GRCh38.p7	19:8566260	GCAAGCTCTGCCTCC[C/G]GGGTTCACGCCATTC	4542
rs370052026	snp	C/T	6.62691e-05	0.00575588	intron-variant	MYO1F	GRCh38.p7	19:8551918	GGTGCTTGCCTGGCT[C/T]AGCCCCTGTGATCCC	4542
rs370081150	snp	A/T	6.60426e-05	0.00574604	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8553215	TTGGACTGCAGGATG[A/T]TATCTTTGACGTGCT	4542
rs370095250	snp	G/T	3.35644e-05	0.00409647	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550199	GGCATAGAGCCCCTT[G/T]GCCAGGGCATCACGG	4542
rs370097600	snp	C/T	2.08492e-05	0.00322865	intron-variant	MYO1F	GRCh38.p7	19:8522588	AGCCCCAGACACTCC[C/T]CTACCCCCTGCCCAC	4542
rs370105681	snp	A/C	0.000150945	0.00868617	missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536392	CGGGGGTCAGAATGG[A/C]ATACCTGAGGGCGGA	4542
rs370134953	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8567267	GATGGGGGTTTCACC[A/G]TCTTGGCCAGGCTGG	4542
rs370167762	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8563461	CACCACCACGCCCAG[C/T]TAACGTTTTGTAATT	4542
rs370187317	snp	A/G	0.00517822	0.0506191	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8529830	AGGTGTGTCTGTGCC[A/G]GGTAATGATGTACCT	4542
rs370246382	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8564316	AACCCAGGAGGCAGA[C/G]GTTGCAGTGAGCCAA	4542
rs370279887	snp	A/T	0.00676609	0.0577691	intron-variant	MYO1F	GRCh38.p7	19:8553870	GACTGAGACTCTGTC[A/T]CACACACACACACAC	4542
rs370292190	snp	A/G	3.35345e-05	0.00409465	missense	MYO1F	GRCh38.p7	19:8521598	CCCTTCCACCAGCCC[A/G]AGGGATCTGTGGGAG	4542
rs370297948	snp	A/G/T	9.95349e-05	0.00705402	synonymous-codon, missense, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530468	TCTCACCTTCCTCCC[A/G/T]CATCTCCTCGTACTT	4542
rs370321661	snp	C/T	0.00034093	0.0130518	intron-variant	MYO1F	GRCh38.p7	19:8555817	GGGTGAGAGGGGGGT[C/T]GGGGTGAGCCCTTGC	4542
rs370325004	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8577165	GGAGGCACCTGAGCT[A/G]CACTGAGAGACACCC	4542
rs370339092	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8570911	CTCAGTTTCCTCATT[C/T]GGAAAATGGGAACAT	4542
rs370361050	snp	A/G	3.34722e-05	0.00409084	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8536451	GACAGGCCTGGCTGG[A/G]CGTTCTGATGAAGGG	4542
rs370497065	snp	C/T	3.31268e-05	0.00406968	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554656	GCCCCAGCCTCACCG[C/T]GCCCTGATAGAGGTC	4542
rs370499673	snp	C/T	0.00597247	0.0543191	intron-variant	MYO1F	GRCh38.p7	19:8522123	CGCCTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT	4542
rs370524390	in-del	-/ACAA			intron-variant	MYO1F	GRCh38.p7	19:8557286	TCTCAAAAAAAACAA[-/ACAA]CCAAACAAACAACAA	4542
rs370525280	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8543537	CAAGCTGGTGTTAAT[C/T]GGGGGGAATTCTGTT	4542
rs370539206	snp	A/G	0.000159987	0.00894248	intron-variant	MYO1F	GRCh38.p7	19:8537061	TGGCTTGTTTCTGAG[A/G]CAGAAGTGAAGACGG	4542
rs370540290	snp	A/G	5.03732e-05	0.00501837	intron-variant	MYO1F	GRCh38.p7	19:8526952	TGGGGAGGGGCGGGT[A/G]AGAGCGTCAGGTGGG	4542
rs370594416	snp	C/T	0.000367317	0.0135471	intron-variant	MYO1F	GRCh38.p7	19:8522625	GAGCTGCCCTCCCAC[C/T]CCACCTACCCGGCCA	4542
rs370622610	in-del	-/A	0.5	0	downstream-variant-500B	MYO1F	GRCh38.p7	19:8520789	AAAAATTTAAAAAAG[-/A]AAAAAAAAAAAAGCC	4542
rs370635638	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8553756	GGGCGCCTGTAATCC[C/T]GGCCACTCAGGAGGC	4542
rs370637953	snp	A/G	5.10704e-05	0.00505298	splice-donor-variant	MYO1F	GRCh38.p7	19:8550158	GCCCCAGCCCCACTC[A/G]CCTCCACGAGGAAGT	4542
rs370642050	snp	C/T			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578631	ATGGGAACGTGGGTC[C/T]CCCCAGCAGAGCCTG	4542
rs370666213	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8541618	AATTTTAGTAGAGAC[A/G]AGGTTTTGCCATGTT	4542
rs370691742	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8569012	AGAGAAAAAATGCGC[C/T]GAGATGCCTCAGGAA	4542
rs370781367	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8570568	GACAGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT	4542
rs370799653	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8560492	CTTGGTCTTAAAAAA[A/G]GGAAAAAAAAAAAAG	4542
rs370826494	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8545306	ATTGGTCAGGCTGGT[A/C]TCGAACTCCTGACCT	4542
rs370839162	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8563421	TCATGCCTCAGCCTC[C/T]TGAGTACCTGGGATT	4542
rs370862976	snp	A/G	0.000744201	0.0192755	intron-variant	MYO1F	GRCh38.p7	19:8553099	TAGAAAGGTCAGCAC[A/G]GAGGGAGCAGCTGCT	4542
rs370908051	snp	A/G	1.65658e-05	0.00287795	missense, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530279	GACGCAGCTCGGGCC[A/G]CTCCTCCAGCCCCAG	4542
rs370910957	snp	G/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8564242	AAAAATTAGCCAGGC[G/T]TGGTGTCAGGCGCCT	4542
rs370938031	snp	C/T	1.65603e-05	0.00287747	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554491	CCTAATGATGACACA[C/T]TGGTTCTCACAGTCG	4542
rs370938191	snp	C/T	1.65603e-05	0.00287747	missense, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8545661	TCACCAGCTTGTTTT[C/T]GATGAGGTCACAGAC	4542
rs370964002	snp	C/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8524484	CAGCTACTCAGGGGG[C/T]TGAGGCAGGAGAATC	4542
rs370964798	snp	C/T	1.65748e-05	0.00287874	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530432	CCTTGTGCCCCCACC[C/T]CGCGCCGTTTACCCG	4542
rs371011867	in-del	-/AAAC			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578057	AAAAAACAAAAAAAC[-/AAAC]CAAAAAAACAACAAC	4542
rs371030678	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8567584	CTCATCTCGAACTCC[A/C]AACCTCAGGTGATCC	4542
rs371067269	snp	A/G	0.000567272	0.0168319	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555784	TCTGCCAGTGGAAGC[A/G]CTCCTTGCTGCCCTG	4542
rs371078620	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8522231	GTTTCACTGTGTTAG[C/T]CAGGATGGTCTCGAT	4542
rs371105289	in-del	-/AAGAAAAA			intron-variant	MYO1F	GRCh38.p7	19:8531361	TCAAAAAAAGAAAAA[-/AAGAAAAA]GACAGGGTCTCGCTC	4542
rs371111771	snp	C/G/T	0.000386268	0.0138929	missense, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526482	AGCCCATCGCCCACG[C/G/T]TGACCGTGAGGGTCC	4542
rs371153488	snp	A/G/T	5.05466e-05	0.00502704	missense, synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544321	GTAGTGGTGGATGAC[A/G/T]AAGCCGGCGCTCCAG	4542
rs371227251	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8574482	ATGGACCATGGAGCG[A/G]GGCATTAGATTTTCT	4542
rs371231029	snp	A/T			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578065	AAAAAAACCAAAAAA[A/T]CAACAACAACAGGGA	4542
rs371266902	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8550997	GCGATTTTCCTGCCT[C/T]CGCCTCCCGAGTAGC	4542
rs371268817	snp	C/G	0.00279162	0.0372561	intron-variant	MYO1F	GRCh38.p7	19:8540186	GAGGGTTGGTTTTTT[C/G]GTTTGTTTTTTGAGG	4542
rs371296248	snp	C/T	0.00358779	0.0422022	intron-variant	MYO1F	GRCh38.p7	19:8535131	TGGCCAGGCTGGTCT[C/T]AAACTCCTGACCTCA	4542
rs371296455	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8559578	ACTACTCTGGGGGAA[C/T]AAGGTGGGATGGGAG	4542
rs371339009	snp	G/T	0.00517822	0.0506191	intron-variant	MYO1F	GRCh38.p7	19:8564777	GTTTCCTGTTTTTTT[G/T]TTGTTGTTGTTTTGA	4542
rs371339136	snp	A/G	6.70275e-05	0.00578872	missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536347	GCTGGACGCCCTGGC[A/G]TTCGTCCCCACGCCA	4542
rs371384589	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8524956	TAATCCCAGCACTTT[C/T]GGAGGCCGAGACGGG	4542
rs371384856	in-del	-/TT			intron-variant	MYO1F	GRCh38.p7	19:8522024	TGTCAGTCAGGGTTC[-/TT]TTTTTTTTTTTTTTT	4542
rs371386719	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8540764	TGCGCAATTCTGTGA[A/G]TTTGCTAAACGTCAT	4542
rs371452030	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8523112	TCTCGGCTCACTGCA[A/G]GCTCCGCCTCCTGGG	4542
rs371484701	snp	A/C	1.65789e-05	0.0028791	intron-variant	MYO1F	GRCh38.p7	19:8551992	GTCCACCCCGCTGGG[A/C]TCCAGGTGGTGCTCC	4542
rs371493415	snp	G/T	0.000591156	0.0171822	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526748	AGGGTGCGCCGCGCC[G/T]AGACCACCCCGAGAT	4542
rs371512663	snp	A/C	0.00438332	0.0466095	intron-variant	MYO1F	GRCh38.p7	19:8563272	TGCTGGGATTATAGG[A/C]ATGAGCCACTGTGCT	4542
rs371583512	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8537294	CCAAGACAAGGAGCT[C/G]TCACGTCTACCGCAC	4542
rs371584475	snp	A/G	1.65526e-05	0.00287681	intron-variant	MYO1F	GRCh38.p7	19:8553442	CACTCTCTCCACTGG[A/G]GATGAATGGAGGAAT	4542
rs371635261	in-del	-/A			intron-variant	MYO1F	GRCh38.p7	19:8568422	GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	4542
rs371664382	snp	A/G	1.67332e-05	0.00289246	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8530539	CGGGCAAAGCCATCG[A/G]ACTTTCGCTCTCGCA	4542
rs371670631	snp	C/G	0.000167986	0.00916323	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8548039	TTGGCCGCCCACCTG[C/G]TCGGCCTTCAGGGTA	4542
rs371681536	snp	C/T	0.000735678	0.019165	intron-variant, missense, utr-variant-3-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536626	TAGGCTGAGTCCCCT[C/T]GGGGTGGGGAGTCAC	4542
rs371689599	snp	C/T	3.31587e-05	0.00407164	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554734	AGATGAGCACAGAGC[C/T]GATGTAGGTCTGAGG	4542
rs371690726	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8544163	ATTGAGGCGGGGGAC[A/G]GTGGAATTCTACAGC	4542
rs371695388	snp	C/T	1.68318e-05	0.00290096	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8526866	GCTGACAAACTCGGT[C/T]TTGAAGACGCTCTCC	4542
rs371717785	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8522302	GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC	4542
rs371718609	in-del	-/TC			intron-variant	MYO1F	GRCh38.p7	19:8533358	TCTTCTTCTTCTTCT[-/TC]TTTTTTTTTTTTTTG	4542
rs371750206	snp	C/T	0.000119924	0.00774257	intron-variant	MYO1F	GRCh38.p7	19:8521633	GAAAGCTTGAGGTGC[C/T]CCTAGCTGGCCCTGG	4542
rs371759403	snp	A/G	1.68826e-05	0.00290534	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8540018	CGGGGAAGAGCATCC[A/G]GAGGAAGGCCCTGGG	4542
rs371806639	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8533146	CGGGCTCAAGGGATC[C/T]TCCCACCTCAGCCAC	4542
rs371885290	snp	A/G	0.000151079	0.00869003	synonymous-codon, missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8539962	CTTGATCTTGGAGCC[A/G]GCGGTGCTGGGGCGC	4542
rs371921083	in-del	-/A			intron-variant	MYO1F	GRCh38.p7	19:8532890	GAGATCCTGTCTCAG[-/A]AAAAAAAAAAAATAC	4542
rs371939581	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8561865	GGGACTATAGGCGCG[C/T]ACCACCACACCCGGC	4542
rs371948427	snp	A/T			intron-variant	MYO1F	GRCh38.p7	19:8553898	CACACACACACACTC[A/T]CTCTCTCTCTCTCTC	4542
rs371998028	in-del	-/C			intron-variant	MYO1F	GRCh38.p7	19:8543414	GGAGGGGCCTGGGGG[-/C]TTTGGGGATTTCCTC	4542
rs372016506	snp	C/T	1.7617e-05	0.00296786	intron-variant	MYO1F	GRCh38.p7	19:8527493	GATGGGCTGTGGGGA[C/T]GCAGGATTAGAGGCT	4542
rs372032112	snp	A/C	3.31983e-05	0.00407407	intron-variant	MYO1F	GRCh38.p7	19:8553484	GGTTGGGGAAGAGCC[A/C]TTTTTAGTGCCTGAC	4542
rs372070342	in-del	-/ATTT			intron-variant	MYO1F	GRCh38.p7	19:8540358	TTTATTTATTTATTT[-/ATTT]CCTTTATTTTTTCTT	4542
rs372083345	snp	C/T	0.000387236	0.0139093	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550318	TCTCCTGCAGTCGCC[C/T]GCTGTCAATGCCCAG	4542
rs372172916	snp	A/G	0.000345925	0.013147	intron-variant	MYO1F	GRCh38.p7	19:8530587	AGCTGGGCGGGGGTC[A/G]TGGGGGGCAAGGGTG	4542
rs372195364	in-del	-/T/TTTTT	0.49907	0.0215454	intron-variant	MYO1F	GRCh38.p7	19:8560742	ACCACGCCTGGCTAA[-/T/TTTTT]TTTTTTTTTTTTTTG	4542
rs372213360	in-del	-/TC			intron-variant	MYO1F	GRCh38.p7	19:8553932	CTCTCTCGCTCTCTT[-/TC]TCTCTCTCTGCTCTC	4542
rs372249160	snp	A/C	0.0023933	0.0345097	intron-variant	MYO1F	GRCh38.p7	19:8564741	AGGCTGTGGGGGAGA[A/C]GTGGGGTCAGGGGAG	4542
rs372260341	snp	A/G	0.000166517	0.00912308	intron-variant	MYO1F	GRCh38.p7	19:8554764	GGATGGTTAAGGGTC[A/G]TGTGGTGTCCTGGTA	4542
rs372332152	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8546924	CCTCAGGTGATCCAC[A/C]CACCTCAGCCTCCCA	4542
rs372342512	snp	C/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8542845	CCTGACCTTGTGATC[C/T]GCCCGCCTCAGCCTC	4542
rs372360560	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8540365	TATTTATTTCCTTTA[G/T]TTTTTCTTTGTCACA	4542
rs372375870	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8554576	TCATACTGGGCCTGG[A/C]AGGGGAGGTCAGGTC	4542
rs372379605	snp	C/T			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578252	CAAGCGATTCTCCTG[C/T]CTCAGCCTCCTGAGT	4542
rs372469776	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8566941	TTCAGCCTATGAAAG[C/T]GCTAGGATTACAGGC	4542
rs372473281	in-del	C/TT			intron-variant	MYO1F	GRCh38.p7	19:8548601	TATTTTCTTTTTTTT[C/TT]TTTCTTTTTTTTTTT	4542
rs372510251	snp	A/G	6.63339e-05	0.00575869	intron-variant	MYO1F	GRCh38.p7	19:8552169	AAGTACTTGCCCTGA[A/G]TCCGAGAGAACCATG	4542
rs372536689	snp	C/T	0.00438332	0.0466095	intron-variant	MYO1F	GRCh38.p7	19:8560399	CTGAGGCAGGAGACT[C/T]GCTTGATCCCGGGAG	4542
rs372567224	snp	A/T			intron-variant	MYO1F	GRCh38.p7	19:8553904	CACACACTCTCTCTC[A/T]CTCTCTCTCTCTCTC	4542
rs372572413	snp	A/G	0.000157988	0.00888644	synonymous-codon, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526499	GACCGTGAGGGTCCG[A/G]CCGCCAACCTTGAGC	4542
rs372580076	snp	A/G			utr-variant-3-prime	MYO1F	GRCh38.p7	19:8521433	AGGCTATTGCAGCCC[A/G]GGTAAACGAGGCTCT	4542
rs372596262	snp	A/C/T	0.000100431	0.00708571	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8536472	TGATGAAGGGGATGG[A/C/T]GAGGGCGGGGGTGGA	4542
rs372670156	snp	A/G	0.0023933	0.0345097	intron-variant	MYO1F	GRCh38.p7	19:8543339	GTCCAGTGGATTTCT[A/G]TAGCCTTCGGTAGGG	4542
rs372684721	snp	G/T	0.000157988	0.00888644	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8526931	AGAAGTCGTCCTGTC[G/T]CGTGCTGGGGAGGGG	4542
rs372763039	snp	C/T	0.000163986	0.00905352	intron-variant	MYO1F	GRCh38.p7	19:8548195	GCCACCCTGGGCTGC[C/T]CCAGGGAGGACAGGA	4542
rs372829266	snp	A/G	0.000259356	0.0113847	intron-variant	MYO1F	GRCh38.p7	19:8577283	CCTCTTTCTTCTTCC[A/G]GATCCCACCCTTGAA	4542
rs372832841	snp	C/T	0.000231961	0.0107669	splice-donor-variant	MYO1F	GRCh38.p7	19:8550561	TGATACCCACACTCA[C/T]GGTCCACACTCTCCA	4542
rs372844037	snp	C/G	1.66599e-05	0.00288611	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8527376	CTGGATGTCCACTTT[C/G]TTCTTCAAGACTTCA	4542
rs372911359	snp	C/T	1.65285e-05	0.00287471	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8553356	TCGTCTCACCTGGAC[C/T]TTCTCGCCTCCGCCA	4542
rs372927680	snp	C/G/T	8.77176e-05	0.00662209	missense	MYO1F	GRCh38.p7	19:8522496	GGCTGGGGCTTGGGT[C/G/T]GGCCCACACCAGGCA	4542
rs372939985	in-del	-/C/T	0.00557542	0.0525036	intron-variant	MYO1F	GRCh38.p7	19:8572278	TGGGCATTTTTTTTT[-/C/T]CCCCTCTGAGACAGA	4542
rs372993877	in-del	-/GAA			intron-variant	MYO1F	GRCh38.p7	19:8532165	ATCTCAAAAAAAAAA[-/GAA]AGAAAGAAAAAGAAA	4542
rs372996862	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8531462	CAAGTGATCCTCCCA[C/T]CTCTGCCTCCTGAGT	4542
rs373084085	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8562726	TTTTTTACAGATGGG[G/T]TCTCCCTATGTTGCC	4542
rs373099666	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8572442	TTGGCTAATTTTTGT[A/G]TTTTTAGTAGAGATG	4542
rs373105274	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8545308	TGGTCAGGCTGGTCT[C/T]GAACTCCTGACCTCA	4542
rs373148939	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8560137	ACGGGACTAAAGATA[C/T]AGGTATTGTTTCCAA	4542
rs373162772	in-del	-/T			intron-variant	MYO1F	GRCh38.p7	19:8548606	CTTTTTTTTTTTTTC[-/T]TTTTTTTTTTTTGAG	4542
rs373165252	snp	C/T	5.04426e-05	0.00502183	missense, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8541979	CGCAGAAGCCGCTGA[C/T]GTCGTAGGAGACCTG	4542
rs373179853	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8546122	TAGGCTGGAGTGCAA[C/T]GGCACGATCTTGGCT	4542
rs373237136	snp	C/T	0.00068235	0.0184583	intron-variant	MYO1F	GRCh38.p7	19:8550706	CACTCTGTGGTACAA[C/T]GGGGGCAGAAACTGT	4542
rs373237499	snp	C/G	1.68252e-05	0.0029004	intron-variant	MYO1F	GRCh38.p7	19:8525466	GAATATAGCAAGGGA[C/G]GCAGCTCCTCACCTC	4542
rs373362851	snp	C/T	3.34795e-05	0.00409129	missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536302	CCATCTGGTACTGGT[C/T]GGGCTCCATGTTGAC	4542
rs373397157	in-del	-/CAAA			intron-variant	MYO1F	GRCh38.p7	19:8528582	AACAAAAAAGAAAAA[-/CAAA]AAAGAAACGAGGTCA	4542
rs373408110	snp	C/T	0.000115945	0.00761308	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555674	GAAGATGTAGTCGTC[C/T]ATGAAGCGCTTCCGG	4542
rs373423000	snp	A/G	1.67725e-05	0.00289585	missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536365	CGTCCCCACGCCACC[A/G]CGGCCACGTCTCGGG	4542
rs373430924	snp	A/G	3.31263e-05	0.00406965	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8552125	TCTTGCCCCCATCTG[A/G]CTCCCCACCTCGGCT	4542
rs373435548	snp	C/T	0.000331945	0.0128787	intron-variant	MYO1F	GRCh38.p7	19:8544477	GCTCTGCGGGGCGAG[C/T]GGGAGCCAGCAGCGG	4542
rs373454385	snp	C/T	1.68094e-05	0.00289904	synonymous-codon	MYO1F	GRCh38.p7	19:8525513	CGCCCGGGTAGGGGC[C/T]TGGGACGACCTCCGA	4542
rs373457402	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8540427	TTAAAATGGTTAATA[A/C]GGCCGGGTGCGGTGG	4542
rs373527508	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8533532	GCTAACTTTTTTGTA[G/T]TTTTTTAGTAGAGAC	4542
rs373531225	snp	C/G	1.65414e-05	0.00287583	intron-variant	MYO1F	GRCh38.p7	19:8553115	GAGGGAGCAGCTGCT[C/G]CAAGCAGGTCTGCAG	4542
rs373615259	in-del	-/G			intron-variant	MYO1F	GRCh38.p7	19:8555407	AAAAAAAAAAAAAAA[-/G]AACAAACAGGGTTGG	4542
rs373620330	snp	A/G			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8577731	TCTCTTTTTAAAACC[A/G]AGGAAGGGGCCCAGG	4542
rs373627527	snp	C/T	8.38736e-05	0.00647532	intron-variant, missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536404	TGGCATACCTGAGGG[C/T]GGAGGGCTGGGGTGT	4542
rs373642029	snp	A/T			intron-variant	MYO1F	GRCh38.p7	19:8541337	CTCAGGTTGCTGGTC[A/T]AAGAACCACATGTCA	4542
rs373675796	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8560888	GGACTACAGGCGCCC[A/G]CCACCACGGCGGCTA	4542
rs373696615	snp	A/G	3.31345e-05	0.00407016	synonymous-codon, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530259	CTCCCTCTTGCCCAG[A/G]AACTGACGCAGCTCG	4542
rs373709768	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8568251	ACACGGTGAAACCCC[A/G]TCTCTACTAAAACTA	4542
rs373721466	snp	G/T	4.71254e-05	0.00485391	utr-variant-3-prime	MYO1F	GRCh38.p7	19:8521492	CCGGCAGGCAGATAG[G/T]CGGGCGAAAGAGAAG	4542
rs373752244	snp	C/T	6.62405e-05	0.00575464	intron-variant	MYO1F	GRCh38.p7	19:8545638	CCCCGCCAAAGTTGA[C/T]CCAGCCCTCACCAGC	4542
rs373777669	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8551353	CACCGTGCCTGGCCT[C/T]TTTTTTTTTTTTTTT	4542
rs373783374	snp	A/G	3.31318e-05	0.00406999	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555713	GGCAATGGCGTCTTC[A/G]GTGATCTGGGGAAGA	4542
rs373789256	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8528165	AGGATGAGGTTGCAG[G/T]GAGCCGAGATCCTGC	4542
rs373839567	snp	G/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8553597	TCTGCTCTCAGCCGG[G/T]CATGGTGGCTCCTGC	4542
rs373905703	snp	A/C/G/T	0.00111038	0.023537	intron-variant	MYO1F	GRCh38.p7	19:8522562	CTGTGGGCACAGGGG[A/C/G/T]TTTGAGTCACAGCCC	4542
rs373914134	snp	C/T	0.000115937	0.00761283	intron-variant	MYO1F	GRCh38.p7	19:8554438	GTTTCAGCAGGGGCC[C/T]GGGCAGCAGGGTCTG	4542
rs373961813	snp	C/T	8.28192e-05	0.00643449	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554671	CGCCCTGATAGAGGT[C/T]GATCTCACGGTCGGT	4542
rs373972277	snp	A/G	4.7453e-05	0.00487075	intron-variant	MYO1F	GRCh38.p7	19:8537067	GTTTCTGAGGCAGAA[A/G]TGAAGACGGGTGGGT	4542
rs373980682	snp	A/G	0.000155988	0.00883004	missense, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530204	GCCTCACCTTGAAGC[A/G]GCGGTCGTACTTGGT	4542
rs374018985	snp	C/T	1.85534e-05	0.00304571	missense	MYO1F	GRCh38.p7	19:8522635	CCCACCCCACCTACC[C/T]GGCCATGCCCTGGTC	4542
rs374031772	in-del	-/CT			intron-variant	MYO1F	GRCh38.p7	19:8546978	GCCACTGCACCCAGC[-/CT]CTCTCTCTCTCTTTG	4542
rs374051040	snp	A/C	1.65603e-05	0.00287747	missense, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8545694	CCTTGTTGTTGAAGT[A/C]CTGGATTGGAGTCCA	4542
rs374065723	snp	C/T	3.30289e-05	0.00406366	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8553225	GGATGATATCTTTGA[C/T]GTGCTGGGGCAGAGG	4542
rs374066540	snp	C/T	0.0138799	0.0821421	intron-variant	MYO1F	GRCh38.p7	19:8543100	GTAGAGACTGGGTTT[C/T]ACCATGTTGGCCAGG	4542
rs374104823	snp	A/G	0.000596928	0.0172658	intron-variant	MYO1F	GRCh38.p7	19:8555818	GGTGAGAGGGGGGTC[A/G]GGGTGAGCCCTTGCA	4542
rs374105823	snp	C/T	8.45559e-05	0.0065016	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550275	CTGCGCCCGCCCCAG[C/T]GGCTGTCCATCTTGC	4542
rs374136737	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8554102	TAGCTGGGGACTACA[A/G]GCGTGCACCACCGTG	4542
rs374157870	in-del	-/CACACACACACACA			intron-variant	MYO1F	GRCh38.p7	19:8553869	AGACTGAGACTCTGT[-/CACACACACACACA]CACACACACACACTC	4542
rs374167304	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8564804	TTGAGACAGAGTCTC[A/G]CTCTGTCACCCAGGC	4542
rs374187061	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8566037	TCACTTGAGCCCAGG[A/G]GTTCGGAGTTACAGT	4542
rs374199180	snp	A/G	8.42708e-05	0.00649063	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544327	GTGGATGACGAAGCC[A/G]GCGCTCCAGCTGTTG	4542
rs374201524	in-del	-/T			intron-variant	MYO1F	GRCh38.p7	19:8570383	CACATTTTTTTTTTT[-/T]ATTTGAGATGGAGTC	4542
rs374205665	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8531674	GATCACAGCTGTGCC[A/G]CTTACTACCTGTGTG	4542
rs374206217	snp	C/T	0.000115918	0.0076122	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8551794	CACCTGGTAGGTGTC[C/T]GATTGGTTGAGGTAG	4542
rs374214765	snp	C/T	0.0138799	0.0821421	intron-variant	MYO1F	GRCh38.p7	19:8522061	GGAGTCTCGCTCTAT[C/T]GCCCAGGCTGGAGTG	4542
rs374244925	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8564359	GCACTTCAGCCTGGG[C/T]GACAGGAGTGAAACC	4542
rs374274277	snp	C/G	0.00182857	0.0301818	intron-variant	MYO1F	GRCh38.p7	19:8539940	CCGTTGTACACCCCA[C/G]GCCCACCTTGATCTT	4542
rs374314114	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8556276	TTCAAGTGATCCACC[C/T]GCCTCAGGCTCCCAA	4542
rs374316191	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8529724	AGATGCATCTGGCCA[G/T]GTGAGGGTGTATCTG	4542
rs374326193	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8549539	TTATTTTGAGACAGA[A/G]TCTCTCTCTGTTGCC	4542
rs374329487	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8533118	TGGAGTGCAGTGGTG[C/T]GATCTCGGCTCCCGG	4542
rs374337845	snp	C/T	0.00026202	0.011443	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8577450	CTTTAGTTCCTCTTA[C/T]AACAGCCCCTTCTCA	4542
rs374342716	snp	C/T	0.000746662	0.0193073	intron-variant	MYO1F	GRCh38.p7	19:8537074	AGGCAGAAGTGAAGA[C/T]GGGTGGGTGGGGGGC	4542
rs374342821	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8524836	GGAATGGGAATTTGA[C/G]AGAGAAGCAGAGAAA	4542
rs374392403	snp	C/T	0.0023933	0.0345097	intron-variant	MYO1F	GRCh38.p7	19:8567608	GTGATCCTCCCACCT[C/T]GGCCTCGCAAAGTGC	4542
rs374473724	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8570612	CCCCAAGTGATCTGC[A/C]CGCCTTGACCTCCCA	4542
rs374544250	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8577250	TTTTTAGGACACCTC[A/C]ACCTGGCTGGTGTCC	4542
rs374569323	in-del	-/T	0.364609	0.222182	intron-variant	MYO1F	GRCh38.p7	19:8551062	GGCTTTGGTTTCCTA[-/T]TTTTTTTTTTTTAGA	4542
rs374597578	snp	G/T	1.848e-05	0.00303968	utr-variant-3-prime	MYO1F	GRCh38.p7	19:8521519	GAAGGCAGTATCCCA[G/T]GGCCCAGCTCAGATC	4542
rs374616064	snp	A/T	1.65605e-05	0.0028775	missense, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8545720	GTCCAGCGGATGCCT[A/T]CCTGCACATACTCCT	4542
rs374636547	snp	A/T			intron-variant	MYO1F	GRCh38.p7	19:8553910	CTCTCTCTCTCTCTC[A/T]CTCTCTCTCTCTCGC	4542
rs374646566	snp	C/G	1.65638e-05	0.00287778	intron-variant	MYO1F	GRCh38.p7	19:8551727	GGGGACTGGAGTAGA[C/G]GCCGGTGCTCACCAG	4542
rs374647158	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8548936	TGATAATAGCAACTA[C/T]CTTATGGGGCTTTTT	4542
rs374649335	snp	A/G			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8579346	AACTTTGGGAGGCTG[A/G]GGTGGGAGGATCGCT	4542
rs374665096	snp	A/G	0.00874735	0.0655527	intron-variant	MYO1F	GRCh38.p7	19:8523118	CTCACTGCAAGCTCC[A/G]CCTCCTGGGTTCACG	4542
rs374749781	snp	C/T	9.28721e-05	0.00681377	intron-variant	MYO1F	GRCh38.p7	19:8525577	TCTGAAAGAAGAGTG[C/T]CAGGGAGTTGAATGA	4542
rs374767520	snp	A/G	0.000729515	0.0190847	synonymous-codon, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530211	CTTGAAGCGGCGGTC[A/G]TACTTGGTGACCGAA	4542
rs374772610	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8525032	GTGAAACCCTGTCTC[C/T]ACTAAAACGATACAA	4542
rs374810051	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8547563	GAGCCGAGATCATGC[C/T]ACTGCACTCCAGCCT	4542
rs374817355	snp	C/T	0.00318978	0.0398085	intron-variant	MYO1F	GRCh38.p7	19:8561026	ATAGGTGTGAGCCAC[C/T]GCGCCTGGCCACGCC	4542
rs374852707	snp	C/T	0.00993419	0.0697739	intron-variant	MYO1F	GRCh38.p7	19:8571757	CACCCGCCACCACGC[C/T]TGGGTAATTTTTTGT	4542
rs374873299	snp	C/G/T	0.000464245	0.0152285	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8548059	CCTTCAGGGTAAGTT[C/G/T]GATAAAGATTTGCTG	4542
rs374884847	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8562355	CTCTGTCACCTAGGC[C/T]GGAGTGCACTGGTGC	4542
rs374911363	snp	C/T	2.20704e-05	0.00332186	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8577486	TTTGGCGGGAGGGGC[C/T]GAGGCCATGGGGGAG	4542
rs374913409	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8522308	ATTACAGGCGTGAGC[C/T]ACCGCGCCCGGCCGA	4542
rs374915218	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8549829	TTTTAGAGACAGGGT[C/T]TTGCTCTGTCACCCA	4542
rs374971527	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8535165	GATCCATCCACCTCA[A/G]CCTCCCAAATTGCTG	4542
rs375030150	snp	C/T	0.000159987	0.00894249	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544381	CGCCTGCAGCTTCTG[C/T]AGCAGTGTCTGGTCT	4542
rs375036959	snp	C/T	1.68607e-05	0.00290346	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8527438	CTTTCTCTCGCCCAA[C/T]CACATACACACACTT	4542
rs375040713	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8535189	ATTGCTGAGATTACA[G/T]GTGTGAGCCAGTGCG	4542
rs375055203	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8526049	AGTCTGTCTCTCTGG[C/T]CGGGCGCAGTGGCTC	4542
rs375056736	snp	C/T	1.65825e-05	0.00287941	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554737	TGAGCACAGAGCCGA[C/T]GTAGGTCTGAGGGAT	4542
rs375065925	snp	C/T	1.67789e-05	0.00289641	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8526878	GGTCTTGAAGACGCT[C/T]TCCAGGAAGCTGTCG	4542
rs375105923	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8572916	TCCCAGGCTGGTCTC[A/G]AACATCTGGCCTCAA	4542
rs375117569	snp	A/T	0.155987	0.23165	intron-variant	MYO1F	GRCh38.p7	19:8553900	CACACACACACTCTC[A/T]CTCTCTCTCTCTCTC	4542
rs375137841	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8561408	CCTTCCTTCCTTTCT[C/T]CTCTCCCTCCCTTCC	4542
rs375202476	snp	G/T	1.65644e-05	0.00287783	intron-variant	MYO1F	GRCh38.p7	19:8554429	GGTGGTGATGTTTCA[G/T]CAGGGGCCCGGGCAG	4542
rs375221696	snp	A/G	5.03419e-05	0.00501681	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8539976	CGGCGGTGCTGGGGC[A/G]CCCCTTCTTGTCTCC	4542
rs375265299	snp	C/T	0.00279162	0.0372561	intron-variant	MYO1F	GRCh38.p7	19:8522171	GGGACTACAGGCGCC[C/T]GCCACCACGCCCGGC	4542
rs375265920	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8564858	GCTCACTGCAACCTC[C/T]GCCTCCCGGGTTCAA	4542
rs375279183	snp	G/T	0.000155988	0.00883004	intron-variant	MYO1F	GRCh38.p7	19:8527299	GCAGCCAGGGGACAG[G/T]TGAGAGTGACTGTGC	4542
rs375376051	snp	A/G	5.33632e-05	0.00516515	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544432	CATGGTGGCGCACAC[A/G]TCGTCCAAGACGCTC	4542
rs375378094	snp	C/T	8.02343e-05	0.0063333	intron-variant	MYO1F	GRCh38.p7	19:8522833	TGCGATCCATGCCTG[C/T]GGCAGGAGCAAGGAT	4542
rs375382085	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8543897	GTGGTGGTGGTGGTG[C/G]TGGTGGTGGTGGTGG	4542
rs375394406	snp	A/G	4.98981e-05	0.00499465	intron-variant	MYO1F	GRCh38.p7	19:8550700	GCATAGCACTCTGTG[A/G]TACAACGGGGGCAGA	4542
rs375412458	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8522244	AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT	4542
rs375463795	snp	A/C/T			intron-variant	MYO1F	GRCh38.p7	19:8574480	CCATGGACCATGGAG[A/C/T]GGGGCATTAGATTTT	4542
rs375465378	snp	C/T	0.000506997	0.0159136	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8530555	ACTTTCGCTCTCGCA[C/T]CTCCTCCAGGAGGAA	4542
rs375476691	in-del	-/C			intron-variant	MYO1F	GRCh38.p7	19:8568457	AAATTAATCACAGGC[-/C]TGTTTGCATCGAAGG	4542
rs375477482	snp	A/C	1.85331e-05	0.00304404	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550320	TCCTGCAGTCGCCCG[A/C]TGTCAATGCCCAGCA	4542
rs375507542	snp	A/C/G	9.19244e-05	0.00677892	missense, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526488	TCGCCCACGCTGACC[A/C/G]TGAGGGTCCGACCGC	4542
rs375551782	snp	A/C	1.6821e-05	0.00290004	intron-variant	MYO1F	GRCh38.p7	19:8539898	CCCCAGGTAGGGTGG[A/C]ACTCAGCCCTCTGCA	4542
rs375553102	snp	A/C	1.65652e-05	0.0028779	intron-variant	MYO1F	GRCh38.p7	19:8554635	GGGGGCTGTGCCTCC[A/C]ACCCAGCCCCAGCCT	4542
rs375558733	snp	A/G	4.97228e-05	0.00498587	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530434	TTGTGCCCCCACCCC[A/G]CGCCGTTTACCCGAA	4542
rs375587564	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8537843	CAAGCGATCAACTGC[C/T]TTAGCCTCCGGAGTA	4542
rs375592561	snp	A/C	2.14567e-05	0.00327535	intron-variant	MYO1F	GRCh38.p7	19:8537059	GTTGGCTTGTTTCTG[A/C]GGCAGAAGTGAAGAC	4542
rs375609608	snp	C/G	3.47874e-05	0.00417043	missense	MYO1F	GRCh38.p7	19:8525553	TTGGCCATTCCCTTC[C/G]GCGTAGGCTCTGAAA	4542
rs375624728	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8546931	TGATCCACCCACCTC[A/G]GCCTCCCAAAGTGCT	4542
rs375670697	snp	A/G	0.000368238	0.013564	intron-variant	MYO1F	GRCh38.p7	19:8550742	GAATCCTGGCCTCCA[A/G]CCTGCCTCCAGGGGC	4542
rs375699074	snp	A/G/T	8.48451e-05	0.00651281	intron-variant	MYO1F	GRCh38.p7	19:8555810	CCCTGGGGGGTGAGA[A/G/T]GGGGGTCGGGGTGAG	4542
rs375704193	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8577982	CTCAGTGAGCCCTGA[C/T]TGCGCCACTGCACTC	4542
rs375715984	snp	A/G	0.0119091	0.0762411	intron-variant	MYO1F	GRCh38.p7	19:8561491	TTTTCTCTTTCTTTC[A/G]TTCTCTTTCTTCTCT	4542
rs375729268	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8574585	TCTTTCTTTCTCTCT[C/T]TCTCTCTCTCTCTTT	4542
rs375735954	snp	C/T	0.00161132	0.0283384	intron-variant	MYO1F	GRCh38.p7	19:8544495	GAGCCAGCAGCGGCT[C/T]AGTTTGGTCTGCCTT	4542
rs375744241	snp	C/T	0.000159987	0.00894249	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550258	TCACATTGATGGACT[C/T]GCTGCGCCCGCCCCA	4542
rs375813144	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8559716	GCACTTTGGGAGGCC[A/G]AGGCGGGGAGATCAT	4542
rs375865729	snp	A/G	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8521793	TGAGCCACTGCATCC[A/G]GCCATTTCTACTCTT	4542
rs375927407	in-del	-/T			intron-variant	MYO1F	GRCh38.p7	19:8561596	TTCCCTCCCTCCCTC[-/T]CTTCTCTTTTTTCTT	4542
rs375967808	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8560434	AGGTTGCAGTGAGCC[A/G]AGATTGCACCATTGC	4542
rs375995051	snp	C/T	0.00900993	0.0665116	synonymous-codon, missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8537038	CATCAGTGTGGCCAC[C/T]AGGTCGTTGGCTTGT	4542
rs376023161	in-del	-/C/TTTTT	0.0147004	0.0845762	intron-variant	MYO1F	GRCh38.p7	19:8551352	CACCGTGCCTGGCCT[-/C/TTTTT]TTTTTTTTTTTTTTT	4542
rs376037505	snp	A/G/T	6.7387e-05	0.00580427	missense, synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544312	CTTGCCAGCGTAGTG[A/G/T]TGGATGACGAAGCCG	4542
rs376065180	snp	A/G	0.000430892	0.0146717	intron-variant	MYO1F	GRCh38.p7	19:8552000	CGCTGGGCTCCAGGT[A/G]GTGCTCCCTCTCCCC	4542
rs376069951	snp	A/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8570166	CAACCTCTGCCTCCC[A/G]GGTTCAAGTGATTCT	4542
rs376071903	in-del	-/A			intron-variant	MYO1F	GRCh38.p7	19:8534177	AGCGAGACTCTGTCT[-/A]AAAAAAAAAAAAAAA	4542
rs376154461	snp	A/G	0.00166095	0.02877	synonymous-codon, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526505	GAGGGTCCGACCGCC[A/G]ACCTTGAGCACTGCC	4542
rs376190192	in-del	-/ATG	0.00478085	0.0486577	intron-variant	MYO1F	GRCh38.p7	19:8553733	AAAAATTAGCCGGAC[-/ATG]GTGGTGGGCGCCTGT	4542
rs376248073	snp	C/T	0.000267966	0.011572	synonymous-codon, missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536972	CTCCCAGTCTCGGGG[C/T]CTCTTGGTCTCGTTG	4542
rs376295033	snp	C/T	0.000430521	0.0146654	intron-variant	MYO1F	GRCh38.p7	19:8551894	AGGGTGTGCCATGTT[C/T]ATGCATCTGGTGCTT	4542
rs376311227	snp	C/G	8.39426e-05	0.00647798	intron-variant	MYO1F	GRCh38.p7	19:8539943	TTGTACACCCCAGGC[C/G]CACCTTGATCTTGGA	4542
rs376324841	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8532043	GAATCGCTTGAACTC[A/G]GGAGGTGGTGGTTGC	4542
rs376377087	snp	A/G	0.000133482	0.00816844	synonymous-codon, missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536540	GCGGTAGGCGAAGCC[A/G]GCTCTGCGCACCCTG	4542
rs376380813	snp	C/T	9.98718e-05	0.00706583	missense	MYO1F	GRCh38.p7	19:8522407	CAATGACCTCGTTCA[C/T]GTTGAAGCTCAGCTC	4542
rs376387166	snp	A/G	0.000182238	0.0095439	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550567	CCACACTCACGGTCC[A/G]CACTCTCCACTCGGG	4542
rs376454294	snp	C/T	6.93001e-05	0.00588602	missense	MYO1F	GRCh38.p7	19:8522697	GAGGGCGGACGTGCC[C/T]GGGGTCGTCTGCTGG	4542
rs376497844	snp	C/T	3.31279e-05	0.00406975	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8552128	TGCCCCCATCTGGCT[C/T]CCCACCTCGGCTGAA	4542
rs376499204	snp	C/T	4.18331e-05	0.00457327	intron-variant	MYO1F	GRCh38.p7	19:8522586	ACAGCCCCAGACACT[C/T]CCCTACCCCCTGCCC	4542
rs376520936	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8541493	GAGTGCAGTGGCACA[A/G]TCTTGGCTCATTGCA	4542
rs376545261	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8524400	CCAGCCTGGGCAACA[G/T]GGCTAGACTCTGTCT	4542
rs376580541	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8538041	CAGTGGCATGATCTC[A/G]GCTCACTGCAACCTC	4542
rs376620902	snp	C/G	1.68661e-05	0.00290392	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8536216	GGGCTCCATGTTGA[C/G]	4542
rs376624737	snp	A/G	1.65644e-05	0.00287783	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555677	GATGTAGTCGTCCAT[A/G]AAGCGCTTCCGGAGG	4542
rs376655905	snp	C/T	1.67377e-05	0.00289284	missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536311	ACTGGTCGGGCTCCA[C/T]GTTGACCGCCCGAAG	4542
rs376658481	snp	A/G	0.0166325	0.0896639	intron-variant	MYO1F	GRCh38.p7	19:8523280	CCTTGTGATCCGCCC[A/G]CCTTGGCCTCCCAAA	4542
rs376683356	snp	C/G	0.000372842	0.0136485	intron-variant	MYO1F	GRCh38.p7	19:8527514	ATTAGAGGCTGATGC[C/G]TGTAGCCTGGCCAGC	4542
rs376794930	snp	C/T	1.65605e-05	0.0028775	missense, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8545711	TGGATTGGAGTCCAG[C/T]GGATGCCTTCCTGCA	4542
rs376824825	snp	A/C	0.000104179	0.00721656	intron-variant	MYO1F	GRCh38.p7	19:8530595	GGGGGTCGTGGGGGG[A/C]AAGGGTGAGTCCTGG	4542
rs376831278	snp	A/G	0.0123036	0.0774623	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8577760	GGGGAGGTGGCTCAC[A/G]CCTGTAATCCCAATA	4542
rs376848758	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8549012	TGGAATGCCAGTGGC[A/G]CAATCTCGGCTCACT	4542
rs376859586	snp	A/G	0.0023933	0.0345097	intron-variant	MYO1F	GRCh38.p7	19:8560186	TGGGTCTATTCAACA[A/G]CAAAGAACAGGTTCT	4542
rs376892184	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8558060	CCTGCTGCCCCTGCC[A/G]TGGCCTTCTCCTCTG	4542
rs376925638	snp	A/G	0.00398564	0.0444627	intron-variant	MYO1F	GRCh38.p7	19:8560984	CCTTGTGATCTGCCC[A/G]CCTCGGCCTCCCAAA	4542
rs376969800	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8568813	GTAGTCTTAGCTATC[C/T]GGGAGGCTGAGGCAG	4542
rs376971437	snp	A/C	1.65353e-05	0.00287531	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8553146	AGACTTACAAAGCGG[A/C]TGGAATTGTTGTTGC	4542
rs376979143	snp	C/T			utr-variant-3-prime, downstream-variant-500B	MYO1F	GRCh38.p7	19:8521077	GGGCTGTGAAAACAT[C/T]GTCCTTGTTGGGCAC	4542
rs376983152	snp	C/T	0.00358779	0.0422022	intron-variant	MYO1F	GRCh38.p7	19:8529435	TGGGGCAGAAGAGGA[C/T]GTGTCTGTTGGTGGA	4542
rs377040493	snp	A/C/G/T	0.001081	0.0232262	intron-variant	MYO1F	GRCh38.p7	19:8552214	TCCTGGGGTGCAGGT[A/C/G/T]GGGGAAGGGTTGGGG	4542
rs377052703	snp	A/T			intron-variant	MYO1F	GRCh38.p7	19:8553906	CACACTCTCTCTCTC[A/T]CTCTCTCTCTCTCTC	4542
rs377109113	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8542189	GGGCTTCCTGGAGAG[A/C]TGATGTTCAAGTTGA	4542
rs377136516	snp	C/T	0.00159617	0.0282053	downstream-variant-500B	MYO1F	GRCh38.p7	19:8520537	TGACCTTGTGATCTG[C/T]CCGCCTCGGCCTCCC	4542
rs377201964	snp	C/T	5.16605e-05	0.00508208	missense	MYO1F	GRCh38.p7	19:8522673	TTGAGGAATTCTGTG[C/T]TGTGCTCTGAGGGCG	4542
rs377212823	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8552692	CAGGAAGTTGCATAG[A/G]TTTTTTTCCCCCCCA	4542
rs377220910	snp	A/G	0.000161477	0.00898401	intron-variant	MYO1F	GRCh38.p7	19:8537081	AGTGAAGACGGGTGG[A/G]TGGGGGGCACAGAGA	4542
rs377261308	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8535342	TATTTCTACCCCGTC[C/G]GTCTTCTCCAAATCA	4542
rs377305745	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8571515	CACCTCCTGGGTTCA[A/G]GCGATTCTCCTGCCT	4542
rs377312930	snp	G/T	0.00398564	0.0444627	intron-variant	MYO1F	GRCh38.p7	19:8555239	GCCAGGCATGGTGGC[G/T]CATGCCTATAATCCC	4542
rs377344389	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8564241	CAAAAATTAGCCAGG[C/T]GTGGTGTCAGGCGCC	4542
rs377360639	in-del	-/C			intron-variant	MYO1F	GRCh38.p7	19:8522002	AGTGGTGGGGTCTGC[-/C]TGGCAATGTCAGTCA	4542
rs377374275	snp	C/T	8.27986e-05	0.0064337	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554551	GAGGGCGTAGATGTG[C/T]GGGGGATTCTCATAC	4542
rs377407935	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8522228	GGGGTTTCACTGTGT[C/T]AGCCAGGATGGTCTC	4542
rs377414145	snp	A/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8562821	TTACAGGCATGAGCC[A/T]TGGTGCCTGGCCAAG	4542
rs377451588	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8555857	CGGCACCTGGCTCAC[C/T]GACGCTATCAGCTTC	4542
rs377470161	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8546168	CTCCCGAGTTCAAGC[A/G]ATTCTCCTGCCTCAG	4542
rs377516253	snp	A/G	4.96364e-05	0.00498154	intron-variant	MYO1F	GRCh38.p7	19:8553094	GTGTGTAGAAAGGTC[A/G]GCACGGAGGGAGCAG	4542
rs377551535	snp	C/T	5.00204e-05	0.00500077	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555783	CTCTGCCAGTGGAAG[C/T]GCTCCTTGCTGCCCT	4542
rs377558428	snp	C/T	0.0304135	0.119506	utr-variant-5-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8577432	CGTTCACCGGACTCC[C/T]GGCTTTAGTTCCTCT	4542
rs377604689	snp	A/G/T	6.62673e-05	0.00575585	missense, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530267	TGCCCAGGAACTGAC[A/G/T]CAGCTCGGGCCGCTC	4542
rs377613765	snp	A/G	0.000434296	0.0147295	intron-variant	MYO1F	GRCh38.p7	19:8527315	TGAGAGTGACTGTGC[A/G]GCAGGTAAGGACCTG	4542
rs377700037	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8551554	ACGGGGTTTAACCAC[A/G]TTGGCCAGGCCGGTC	4542
rs377727512	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8539095	GACCAGCCTGGCCCA[C/T]ATGGTGAAACCCCAT	4542
rs377729216	snp	C/G			intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8529771	TACAAGTGCATGTTT[C/G]ATGGACAGCTGTGTC	4542
rs377736416	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8559952	CAAAACTCCATCTCA[A/G]AAAAAAAAAAAAAAA	4542
rs377743909	snp	C/T			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578227	TACTTTAATCTCCGC[C/T]TCCTGGGTTCAAGCG	4542
rs386388507	in-del	-/T			downstream-variant-500B	MYO1F	GRCh38.p7	19:8520784	CACCCGGCTTTTTTT[-/T]TTTTTCTTTTTTAAA	4542
rs386806592	multinucleotide-polymorphism	CT/TC			intron-variant	MYO1F	GRCh38.p7	19:8521912	CTCCTGCCTCAGCCA[CT/TC]GAAAGTGCTGGGATT	4542
rs386806593	multinucleotide-polymorphism	GC/TA			intron-variant	MYO1F	GRCh38.p7	19:8545511	GGACATTTTGGTTGT[GC/TA]TCTGTCGCTGGAAGT	4542
rs386806594	in-del	ATGAGGTGCAG/GAA			intron-variant	MYO1F	GRCh38.p7	19:8552615	TGCAGGTGTAATACT[ATGAGGTGCAG/GAA]GTCTATGAGATGGAT	4542
rs386806595	multinucleotide-polymorphism	CA/TG			intron-variant	MYO1F	GRCh38.p7	19:8564443	GTCCCTGGGGTGCGT[CA/TG]GGAGATGACAGAATC	4542
rs397786565	in-del	-/TC			intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8536185	CTCTCTCTCTCTCTC[-/TC]AGTCCCTCTCTATAC	4542
rs397807715	in-del	-/A			intron-variant	MYO1F	GRCh38.p7	19:8539606	TCTCAAAAAAAAAAA[-/A]TTATTGGATATTATT	4542
rs398033853	in-del	-/A	0	0	intron-variant	MYO1F	GRCh38.p7	19:8523049	GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAGT	4542
rs398033854	in-del	-/T	0	0	intron-variant	MYO1F	GRCh38.p7	19:8524599	ACCAAAAATTCTTTC[-/T]TTTTTTTTTTTTTTT	4542
rs398120796	in-del	-/A			intron-variant	MYO1F	GRCh38.p7	19:8560506	AGGAAAAAAAAAAAA[-/A]GAACAGGTTCTTGCC	4542
rs527280948	snp	C/T	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8525660	CCGCCGCACCCCGCC[C/T]CCTCAGGCTCTCCCA	4542
rs527289222	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578483	GTCACACGTGTTTGT[A/G]TGCAGAAGTGGAGGG	4542
rs527292701	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8571731	GCCTCCCAAGTAGCT[A/G]GGACTACAGGCACCC	4542
rs527318899	snp	A/G	0.00478085	0.0486577	intron-variant	MYO1F	GRCh38.p7	19:8531412	GGAGTGTGGTGGTGC[A/G]GTCATAGCTCACTGC	4542
rs527342590	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8526132	ATGAGTTCAAGACCA[G/T]CCTGGCCAAGATGGT	4542
rs527351884	in-del	-/AAAAAAAG	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8531348	GCAAAACTTCATCTC[-/AAAAAAAG]AAAAAAAGAAAAAGA	4542
rs527415617	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8565811	ACAGTTAACACCTGG[A/C]CGGGTGGTGGCTCAC	4542
rs527428465	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8563840	TTCTATGTTGGCCAG[G/T]CTGGTCTCAAACTCC	4542
rs527450929	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8560800	CTGGAGCGCAGTGGC[A/G]CGATCTCGGCTCACT	4542
rs527503546	snp	C/T	0.0023933	0.0345097	intron-variant	MYO1F	GRCh38.p7	19:8522083	GCTGGAGTGTGTTGG[C/T]GCAATCTCGGCTCAC	4542
rs527608331	snp	A/G	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8555052	TACCCGGGCATGGTG[A/G]TGCATGCCTGTAATC	4542
rs527757990	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8539166	ACACCTGTAATCCCA[A/G]CGCTTTGGGAGGCTG	4542
rs527824284	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8543891	CTGGTGGTGGTGGTG[C/G]TGGTGCTGGTGGTGG	4542
rs527825363	snp	G/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8572882	TAAATGCTTTGTAGA[G/T]ATGGGGTATTGCCAT	4542
rs527878299	snp	C/T	0.00398564	0.0444627	intron-variant	MYO1F	GRCh38.p7	19:8527723	GCTTGAGTGATCCAC[C/T]TGCCTCAGCCTCCTG	4542
rs527893766	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8561951	TGAACTCCTGACCTC[A/G]TGATCCACCCATGTC	4542
rs527893940	in-del	-/TT			intron-variant	MYO1F	GRCh38.p7	19:8574603	TCTCTCTCTCTTTCT[-/TT]CTTTCTTTCTTTCTT	4542
rs527915768	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8533284	TCTACCAGCCTTGAC[C/T]TCCCAAAGTGCTGGG	4542
rs527940632	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8528192	CTGCCACTGCACTCC[A/C]GCCTGGGTGACAGAG	4542
rs527980814	snp	C/T	0.000265006	0.0115079	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555664	CCCAGGGTACGAAGA[C/T]GTAGTCGTCCATGAA	4542
rs528095955	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8523085	CGCTCAGGCTGGAGT[A/G]CAGTGGCGCGATCTC	4542
rs528141553	in-del	-/TCAGGTAAAGGTATTATGGT	0.00199481	0.0315187	intron-variant	MYO1F	GRCh38.p7	19:8528758	GTGACTGTAGCCAGC[-/TCAGGTAAAGGTATTATGGT]TCAGGTGAGGGTGTA	4542
rs528169101	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8551152	CACCTCCCGGGTTTA[A/G]GCGATTCTCCTGCCT	4542
rs528344423	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8534974	TTGAGTGCAGTGGCA[C/T]GATCTTGGCTCACTT	4542
rs528354232	snp	A/G			missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8526825	AGGGGCCTCCGCGTC[A/G]CCTCCTCGAAGCGCT	4542
rs528367088	snp	C/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8568889	TTACGTCATTGCACT[C/G]CAGCCTGGGCAACAG	4542
rs528410545	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8575085	TTCTTTTTCTTTTTT[C/T]TTTTTTTTTGAGACG	4542
rs528421520	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8571997	TAAAGTATTGGGATT[A/G]CAGGCGTAAGCCACC	4542
rs528428717	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8569541	ACTTCCTGGGCCCCT[A/G]CTGTGCATGGAGGTA	4542
rs528551727	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8523433	CTGCAACTCTGACCT[C/T]CTGGGCTCAAGCAAT	4542
rs528592601	snp	A/G	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8562902	TAAAAATGACCTGTA[A/G]GTGGGACTGTCATAC	4542
rs528677408	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8535201	ACAGGTGTGAGCCAG[C/T]GCGCCTGGCCAGCAA	4542
rs528794222	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8523180	GGGACTACAGGCACC[C/T]GCCACCACGCCTGGA	4542
rs528829058	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8549056	CCAGGATTCAAGAGA[G/T]TCTTCTGCCTCAGCC	4542
rs528860893	snp	C/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8545854	TCTGGTAACAAAGCC[C/T]GTCACTCCTATGTGG	4542
rs528899948	snp	A/G	0.00199481	0.0315187	intron-variant	MYO1F	GRCh38.p7	19:8522285	CCTTGGCCTCCCAAA[A/G]TGCTGGGATTACAGG	4542
rs528923344	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8563400	CTTCCCGGATTCAAG[C/T]GATTCTCATGCCTCA	4542
rs528969000	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8555597	TTCACCCTCCTCTCC[A/G]TCCATGGCCCAGCCA	4542
rs529213453	snp	C/T	0.0182019	0.0936463	intron-variant	MYO1F	GRCh38.p7	19:8568295	AGGTGCGGTGGCGGG[C/T]GCCCGTAGTCCCAGC	4542
rs529217584	snp	A/G	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8575016	CCACCTCGGCCTCCA[A/G]AAGTGTTGAGATTAC	4542
rs529296158	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8528338	TTGAGACCATCCTGG[C/T]TAATACCATGAAACC	4542
rs529357123	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8562259	GCCCGCCTTGGCCTC[A/C]CAAAGCACTGGGATT	4542
rs529373785	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8568798	TGGTGGCGGGTGTCT[A/G]TAGTCTTAGCTATCC	4542
rs529470889	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8523389	TCACTCTCGCCCAGG[C/T]TGGAGTGCAGTGGTA	4542
rs529588905	snp	A/G	3.31285e-05	0.00406978	intron-variant	MYO1F	GRCh38.p7	19:8551731	ACTGGAGTAGAGGCC[A/G]GTGCTCACCAGAGTC	4542
rs529629257	snp	A/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8551329	AGTGCTGGGATTACA[A/G]GTGTGAGCCACCGTG	4542
rs529655396	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8549111	ATGCGCCACCACGCC[C/T]GGCTAATTCTTGTAT	4542
rs529668873	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8550834	CTTTCAGTCACTTGC[C/T]GCGTGACCTTGGGTA	4542
rs529704674	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8535338	TCATTATTTCTACCC[C/T]GTCCGTCTTCTCCAA	4542
rs529726990	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8535625	AAATTTTTGGTCTAT[G/T]TCTTCCAGAGTGTCT	4542
rs529815277	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8546660	TGATTGTGTCTGGCT[C/T]GGTCTGTCTCTCTCT	4542
rs529890964	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8530869	ACATAGTGAAACCCC[A/G]TCTCTACTAAAAATA	4542
rs529936410	snp	C/G	0.132066	0.220435	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8536167	TCTCTGTCTCCCTCT[C/G]TCTCTCTCTCTCTCT	4542
rs530050667	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8524742	GAGTGGCTTTGCAGG[C/G]GCAAGTTTCCCTCCT	4542
rs530054537	snp	A/G	0.00279162	0.0372561	intron-variant	MYO1F	GRCh38.p7	19:8559142	GCCTCGATCTTCCAA[A/G]CTGCTGGGATTACAG	4542
rs530112645	snp	C/T	0.00199481	0.0315187	intron-variant	MYO1F	GRCh38.p7	19:8547628	AAAAAAAATCCCTGA[C/T]TTACTTCCTCAGTCT	4542
rs530115310	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8553744	GGACATGGTGGTGGG[C/T]GCCTGTAATCCCGGC	4542
rs530165604	in-del	-/C	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8557290	AAAAAAAACAAACAA[-/C]CAAACAAACAACAAA	4542
rs530207776	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8543912	CTGGTGGTGGTGGTG[C/G]TGGTGGTGGTGGTGG	4542
rs530251555	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8531866	CTCAAGCCTGTAATC[C/T]CAGCATTTTGGGAGG	4542
rs530278950	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8542139	TACAGCGCTGGCTGG[C/G]GGGTATCTACAGTTC	4542
rs530327950	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8544779	ACCTGCCTTATGTAT[G/T]TATTTATTTATTTAG	4542
rs530362879	in-del	-/T			intron-variant	MYO1F	GRCh38.p7	19:8562044	TTTTTTTTTCTTTTG[-/T]TTTTTTTTGAGATGG	4542
rs530464156	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8577986	GTGAGCCCTGATTGC[A/G]CCACTGCACTCCAGC	4542
rs530512589	snp	A/G	0.00398564	0.0444627	intron-variant	MYO1F	GRCh38.p7	19:8523226	TTTTAGTAGAGACGG[A/G]GTTTCATCATGTTAG	4542
rs530525027	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8545855	CTGGTAACAAAGCCC[A/G]TCACTCCTATGTGGG	4542
rs530594446	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8546167	CCTCCCGAGTTCAAG[C/T]GATTCTCCTGCCTCA	4542
rs530612663	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8535552	TGATATTACAGGCAT[A/G]CGCTACCACACCTGA	4542
rs530638593	snp	A/G	0.00358779	0.0422022	intron-variant	MYO1F	GRCh38.p7	19:8551587	AAACTCCTGACCTTA[A/G]GTGATCTACCTGCCT	4542
rs530646424	snp	A/C	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8540670	AGCCGAGATCGTGCC[A/C]CTGCACTCCAGCCTG	4542
rs530651799	snp	C/T	0.00597247	0.0543191	intron-variant	MYO1F	GRCh38.p7	19:8537208	GCCAGATGTCCCTGG[C/T]CTGTGTGCACCTCCA	4542
rs530672611	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8536043	TTTCAGTCTATTAAT[C/G]TCTCACTTGCTTTCT	4542
rs530687787	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8556090	CTGGGGTGCAGTGGC[A/G]TGATCTCTGCTCACT	4542
rs530712828	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8563011	CCTTTTTTTGTTTTG[A/C]TACCGAGTCTCACTC	4542
rs530746637	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8569580	CCAGGCTTAGGTGGA[A/C]CAGGCCCAGAACCTG	4542
rs530816844	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8574387	CTACCATGGATCAAG[C/T]GCATGTTATGTGCTC	4542
rs530824264	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8523688	GAGACAGGGTTTTGC[C/T]CTGTGGCCCAGGATG	4542
rs530829291	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8570211	CCAAGTAGCTGGGAT[C/T]ACAGGCGTGCACAAC	4542
rs530852708	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8575767	GTGGCCCCTCCCAGA[C/T]CTTGTCTGCCAAGCC	4542
rs530854618	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8554162	GGATGTTGCCATATT[A/G]CCCAGGCTGGTCTTG	4542
rs530863936	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8550135	CAGAGCATCCACTCT[A/G]CCTTCCAGCCCCAGC	4542
rs530875155	in-del	-/CTCT			intron-variant	MYO1F	GRCh38.p7	19:8553895	ACACACACACACACA[-/CTCT]CTCTCTCTCTCTCTC	4542
rs530895814	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8563612	CTCCCGGGTTCAAGC[G/T]ATTTTCCTGCCTCAG	4542
rs530899226	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8558971	GCTACCTCTGCCTGC[A/G]GGGCTCAAGCGAGCC	4542
rs530911904	snp	A/C	0.0023933	0.0345097	intron-variant	MYO1F	GRCh38.p7	19:8524039	CAGGAGAATTGCTTC[A/C]ACCTGGGAGGTGGAG	4542
rs531014456	snp	C/T	0.00358779	0.0422022	downstream-variant-500B	MYO1F	GRCh38.p7	19:8520582	ACAGGTGTGAGGCAC[C/T]GCGCCCACCTCCTCC	4542
rs531147218	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8537154	CCAATAGACAGAGAC[C/T]GGGGGTGGGTGAGGG	4542
rs531200409	snp	A/C	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8542081	CCCAGGTGGTCAAGG[A/C]TTTCCTGGGGCCTGC	4542
rs531236647	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8542683	TCAGCTCACTGCAAC[C/T]TCCGCCTTCCGGGAT	4542
rs531246169	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8547590	GCCTGGGTGACAGAA[C/T]GAGACTTTGTCTCAA	4542
rs531321104	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8531052	TCCATCTCAAAAAGA[C/T]AAAAAACAAAAACAA	4542
rs531340057	snp	C/G	0	0	intron-variant	MYO1F	GRCh38.p7	19:8571634	ACGGAGTCTTGCTCT[C/G]TCACCCAGGCTGGAG	4542
rs531360716	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8536684	GGAGGTGGGGGACCT[A/G]GGGGGATCTGGATTC	4542
rs531365076	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8565631	GGCAGGAGCAGGGTC[A/G]TGAGTGGTGAGGGTC	4542
rs531385418	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8526094	AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGAGCA	4542
rs531390286	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8531379	AAAAAGACAGGGTCT[C/T]GCTCCGTCGCCCAGA	4542
rs531396535	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8568467	ACAGGCTGTTTGCAT[C/T]GAAGGGAGAGAGGGT	4542
rs531545916	snp	A/G	0.00199481	0.0315187	intron-variant	MYO1F	GRCh38.p7	19:8522046	TTTTTTTTTTGAGAC[A/G]GAGTCTCGCTCTATC	4542
rs531579598	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8543729	GTGGTGGTGGTGCTG[A/G]TGGTGCTGGTGGTGC	4542
rs531599660	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8543880	TGCTGGTGGTGCTGG[C/T]GGTGGTGGTGGTGGT	4542
rs531662535	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8553991	AGATGGGGTCTCACT[C/G]TGTTGCCCAGGCTGG	4542
rs531718375	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8560357	GGGTGTGGGGGTGCG[C/T]GCCTGTAATCCCAGC	4542
rs531745227	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8579112	CTGGAGTTAAAAAAG[A/G]TAAAGGGGCAGGAGC	4542
rs531776261	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8532649	CCCAGCAGTTTGGGA[A/G]GCTAAGGTGGGAGCA	4542
rs531787107	snp	C/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8548829	TCCTGACCTCGTGAT[C/T]CGCCCGCCTCGGCCT	4542
rs531853653	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8549198	CTTGGGTGATCTGCC[C/T]GCTTTGACCTCCCAA	4542
rs531908955	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8572818	TTCCCACCTCAGCTT[C/T]CCAATTAGCTGGTAC	4542
rs531952791	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8537291	AACCCAAGACAAGGA[C/G]CTCTCACGTCTACCG	4542
rs531986426	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8576824	CAGAACCCACAGACC[C/T]TGAGAATGTTGCAAC	4542
rs531989631	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8538894	GGGGACACAGTTTCA[G/T]TTTGGGAAGATGAGA	4542
rs532022505	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8560983	ACCTTGTGATCTGCC[C/T]GCCTCGGCCTCCCAA	4542
rs532052345	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8547510	TCGGGAGGCTGAGGC[A/C]GGAGAATCACTTGAA	4542
rs532057995	snp	C/T	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8566552	AGAGTGTTGCTCTTT[C/T]GCCCTGGCTGGAGTG	4542
rs532070983	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8549638	CTCCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAA	4542
rs532072109	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8573251	AGGAGGTGGGGCTTG[C/T]AGTGAGCCAAGATCA	4542
rs532105665	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8550928	CTCTGTTGCCCAGGC[C/T]GGAGTGCAGTGGTAT	4542
rs532143827	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8570411	GTCTCGCTCTTGTTG[C/T]TCAGTCTGTGAGTGC	4542
rs532204636	snp	A/G	9.79691e-05	0.00699821	intron-variant, stop-gained, utr-variant-3-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536627	AGGCTGAGTCCCCTC[A/G]GGGTGGGGAGTCACC	4542
rs532235231	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	MYO1F	GRCh38.p7	19:8520860	GAACTCCTGGTCTCA[C/T]GTGATCTGCCCGCCT	4542
rs532289487	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8569769	GCCAGAGAGGCCTTG[A/G]GTGTGTGGTGGACAC	4542
rs532304480	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8564295	CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG	4542
rs532369219	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8531013	CGCGCCATTGCACTC[A/C]AGCCTGGACAACAAG	4542
rs532432141	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8559819	GCTGGGCGTGGTGGC[A/G]CACGCCTGTAATCCC	4542
rs532439270	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8542745	AGCTGGGATTACAGG[C/T]GTGTGCCACCACACC	4542
rs532470178	in-del	-/AAAA			intron-variant	MYO1F	GRCh38.p7	19:8540711	GAGAGACACTGTCTC[-/AAAA]CAAAAAAAAAAAAAA	4542
rs532568927	snp	C/T	0	0	intron-variant	MYO1F	GRCh38.p7	19:8531946	AACATGGTGAAACCC[C/T]GTCTCTACTAATAAT	4542
rs532637570	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8538354	GGCTGGAGTGCAGTG[A/G]CTCTTGGCTCACTGC	4542
rs532749700	snp	A/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8566490	GCTTTTTAAAAAAAA[A/T]TTTATTTTTATTTAT	4542
rs532823633	snp	A/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8532541	AACATCCTACTTCAA[A/T]GAGAAACTGTGATCA	4542
rs532845731	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8563663	ACAGGAGCCCATCAA[C/T]ACGCCCAGCTAATTT	4542
rs532846972	snp	G/T	0.00199481	0.0315187	intron-variant	MYO1F	GRCh38.p7	19:8555090	CTTGGGAGGCTGAGG[G/T]AGGAGAATCGCTTGA	4542
rs532848538	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8561168	GGATTACAGGTGTGA[A/G]CCACTGTGCCTGGCC	4542
rs532878192	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8572345	CGATCTCAGCTCACT[A/G]CAACCTCTGCCTCTC	4542
rs532978040	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8526157	GATGGTGAAACCCCG[C/T]CTCTACTAAAACTAC	4542
rs533003053	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8555532	TGTCACTCTGTCTGT[C/G]CTCTGTGTCACCACT	4542
rs533010922	in-del	-/TTT	0.00199481	0.0315187	intron-variant	MYO1F	GRCh38.p7	19:8545281	TTTAGTAGAGACAGG[-/TTT]TCACCATATTGGTCA	4542
rs533011270	snp	A/G	0.0107246	0.0724382	intron-variant	MYO1F	GRCh38.p7	19:8540092	GGGTACTCTTCCTCC[A/G]GGGGTGGGGCAGCCT	4542
rs533019602	snp	C/T	0.00199481	0.0315187	intron-variant	MYO1F	GRCh38.p7	19:8522264	CCTGACCTCGTGATC[C/T]GCCCGCCTTGGCCTC	4542
rs533073184	in-del	-/T	0.00676609	0.0577691	intron-variant	MYO1F	GRCh38.p7	19:8538765	CTAATTTTTAATTTA[-/T]TTTTTTATAGAGACG	4542
rs533079893	snp	C/T	0.00199481	0.0315187	intron-variant	MYO1F	GRCh38.p7	19:8559675	ATTAACACGACCGGG[C/T]GCGGTGGCTCACACC	4542
rs533083582	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8572855	TCCATGCCACCATGC[C/T]TGGCTAACTTTTAAA	4542
rs533084662	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8550069	CCACCCAAAGCATTG[A/G]GATTGCAGCCGTGAG	4542
rs533119990	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8522136	CATGCCATTCTCCTG[C/T]CTCAGCCTCCCGAGT	4542
rs533265906	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8568249	TAACACGGTGAAACC[C/T]CGTCTCTACTAAAAC	4542
rs533283700	in-del	-/C	0.00398564	0.0444627	intron-variant	MYO1F	GRCh38.p7	19:8522001	CAGTGGTGGGGTCTG[-/C]CTGGCAATGTCAGTC	4542
rs533419501	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8533947	CCCAGCACTTTGGGA[A/G]GCTGAGGTGGGCAGA	4542
rs533526438	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8561981	CGGCCTCCCAAAGTG[C/G]TGGGATTACAGGCAT	4542
rs533568289	snp	G/T	0.00279162	0.0372561	intron-variant	MYO1F	GRCh38.p7	19:8528954	AGTTCTCTGGGTCTA[G/T]TGGGGATACCTGTCT	4542
rs533611108	snp	A/G	0.000190931	0.00976877	utr-variant-3-prime	MYO1F	GRCh38.p7	19:8521498	GGCAGATAGGCGGGC[A/G]AAAGAGAAGGCAGTA	4542
rs533740564	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8545413	TGACTCTAACTGTGA[A/G]CTGGGGTTCCCGGGG	4542
rs533748161	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8559471	CTGGGTTCTGATCCT[A/G]ACTGGGCAAACAGAT	4542
rs533774083	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8532066	GTGGTTGCAGTGAGC[A/G]GAGATTGCGCCACTG	4542
rs533777844	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	MYO1F	GRCh38.p7	19:8521105	CACTTAGTAAGTTAA[C/G]TCGTGCTTTCACCTG	4542
rs533864833	snp	A/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8547932	GAGAGGTGGGAACGC[A/G]GTGGGGAGGGCTGGG	4542
rs533909451	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8543994	TGGTGCTGGTGGTGG[C/T]GCTGGTGGTGGCGGT	4542
rs533919113	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8553579	AACAAGACAGATAAA[A/G]TCTCTGCTCTCAGCC	4542
rs533951418	snp	C/G	0.00119737	0.0244387	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8579029	GGTAAGAGGACCCCA[C/G]TTTGTTGGGGGCCAT	4542
rs533984213	snp	C/T	0.00199481	0.0315187	intron-variant	MYO1F	GRCh38.p7	19:8538045	GGCATGATCTCGGCT[C/T]ACTGCAACCTCCGTC	4542
rs534042462	snp	C/T	0.00199481	0.0315187	intron-variant	MYO1F	GRCh38.p7	19:8532074	AGTGAGCGGAGATTG[C/T]GCCACTGCACTCCAG	4542
rs534063663	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8543637	CTGGCCCAGGGAACA[C/T]GGTGGTGGTGGTGGT	4542
rs534143745	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578274	CTCCTGAGTAGCTGG[A/G]ATTACAGGTGCCCAC	4542
rs534154638	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8572530	GCCTCGGCCTCCTAA[A/G]GTGCTGGGATTACAG	4542
rs534159217	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8522191	CCACGCCCGGCTAAT[G/T]TTTTGTATTTTTAGT	4542
rs534214839	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8549608	ACCTCCACCTCCCAG[G/T]TTCAAGTGATTCTCC	4542
rs534295605	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8560654	GTCATGGCTCACTGC[A/G]GCCTTGACCTCCTGG	4542
rs534321167	snp	C/G	0.00199481	0.0315187	intron-variant	MYO1F	GRCh38.p7	19:8566252	GGCTCACTGCAAGCT[C/G]TGCCTCCCGGGTTCA	4542
rs534356429	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8560989	TGATCTGCCCGCCTC[A/G]GCCTCCCAAAGTGCT	4542
rs534366572	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8569835	TCCTGGAGGGATAGA[C/T]AGCCCAGGCCATGTG	4542
rs534395465	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8539424	CATCTCAAAAAAAAA[A/C]CCAAACCAACAAAAA	4542
rs534396359	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8566729	ATGTTGGCCAAGCTG[A/G]TTTCGAACTCCTGAC	4542
rs534431035	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8545031	GATCCACCTGCCTTG[G/T]CCTCCCAAAGTGCTG	4542
rs534457899	snp	A/G	0.00318978	0.0398085	intron-variant	MYO1F	GRCh38.p7	19:8555577	CCCATTCCTCCCTCT[A/G]CTCCTTCACCCTCCT	4542
rs534474401	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8536003	TCTTTCTTAATCTCT[C/T]GCTCAGTCTCTCTCA	4542
rs534480371	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8567764	GACCCACGAAGCTGT[C/T]CTTCCCCAGGCTGGT	4542
rs534512126	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8537682	CAGGTGATCCATCCA[C/T]CTCTGGCTCCCAAGG	4542
rs534529428	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8574074	CTCCAAATAACAGCA[A/G]CCACCGATGGTCATC	4542
rs534561806	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8533637	GCTGGGAATTACAGG[C/T]GTGAGCCAGCACGCT	4542
rs534645939	in-del	-/AAAAAAAAAAAAA			intron-variant	MYO1F	GRCh38.p7	19:8556898	GTCTCAAAAAAAAAA[-/AAAAAAAAAAAAA]GGAAGCCAATCTGAA	4542
rs534790397	snp	C/T	0.00279162	0.0372561	intron-variant	MYO1F	GRCh38.p7	19:8574538	TTTTTTCCCTTTCTT[C/T]CTTTCTTTCTTTCTT	4542
rs534826510	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8550983	CATCCCAGGTTCAAG[C/T]GATTTTCCTGCCTCC	4542
rs534923679	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8528040	CAGGCTGACCAACAT[A/G]GTGAAACCCCGTCTC	4542
rs534924400	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8534137	TGAGCCAAGATTGCG[C/T]CATTCCACTTTAGCC	4542
rs535034502	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8555185	CACTCAGTCTCAAAA[A/G]CAAAACACAAAACAC	4542
rs535052540	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8575378	CCGCACCCGGCCGGG[C/T]ATTAGATTGTCATAA	4542
rs535057022	snp	C/G	0.00318978	0.0398085	intron-variant	MYO1F	GRCh38.p7	19:8559192	GCCCAGGATTGAAGT[C/G]TTTAAAGTGGACTGT	4542
rs535100088	snp	C/T	0.00281237	0.0373935	intron-variant	MYO1F	GRCh38.p7	19:8551352	CCACCGTGCCTGGCC[C/T]TTTTTTTTTTTTTTT	4542
rs535139064	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8557054	ACTTTGGGAGGCCGA[C/G]GCGGGAGGACTGCTT	4542
rs535188425	snp	G/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8544539	TCGTCAGTGCAGAGA[G/T]TAGGGGAGGGAGGGG	4542
rs535279954	in-del	-/T/TT	0.491525	0.0645418	downstream-variant-500B	MYO1F	GRCh38.p7	19:8520777	ACCACCACACCCGGC[-/T/TT]TTTTTTTTTTTTCTT	4542
rs535403200	snp	A/G	0.00676609	0.0577691	intron-variant	MYO1F	GRCh38.p7	19:8573839	GGGGTGACAGAGCGA[A/G]ACTCTGTCTCAGAAA	4542
rs535445367	snp	C/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8561624	CTTTCTCTCTTTCTT[C/T]CTTCTTTCTTTCCTT	4542
rs535577176	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8555129	GGCAGAGGTTGCAGC[A/G]AGCTATCGTGCCATT	4542
rs535601564	snp	C/G	0.00279162	0.0372561	intron-variant	MYO1F	GRCh38.p7	19:8539525	CACTTGAACCCAGGA[C/G]GCGGAGGTTGCAGAG	4542
rs535620553	in-del	-/AGTT	0.000433117	0.0147096	intron-variant	MYO1F	GRCh38.p7	19:8550390	GGGCAAAAATGGGAC[-/AGTT]GGTTGGGCTCTTGTG	4542
rs535752837	snp	A/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8539333	GCAGGAGAATCACTT[A/G]AACCCAAGAGGCAGA	4542
rs535759345	snp	C/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8532781	TAGTCCCAGCTATTC[C/T]GGAGGGTGAGGTGGG	4542
rs535783668	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8567001	CTTTTTATGTGAATT[A/G]CTTCATCTTATCCTT	4542
rs535846412	snp	A/G	0.0023933	0.0345097	intron-variant	MYO1F	GRCh38.p7	19:8533600	CTGACCTCATGATCC[A/G]CCTGCCTCGGCCTCC	4542
rs535878648	snp	A/G	0.00279162	0.0372561	intron-variant	MYO1F	GRCh38.p7	19:8527917	CACGCCTGGCCATGA[A/G]TTGTTATATAAGAAA	4542
rs535896563	snp	A/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8523153	TCTCCTGCCTCAGCC[A/T]CCCGAGTAGCTGGGA	4542
rs535916711	snp	A/G	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8529473	AGCTGTCTATGCCAA[A/G]CATGAATGCACGGGT	4542
rs535947077	in-del	-/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8565860	TTGGGAGGCTGAGGT[-/G]GAAGGATCACTTGAG	4542
rs535981500	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8556616	TCTGGGGCCGGGCAC[A/G]GTGGCTCATGCCTGT	4542
rs536005354	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8550874	ACCTCTCTGGGCTTT[A/G]TTTTTTATTATATTT	4542
rs536034914	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8523769	ATGATATTCTCCCCT[C/T]TCAGCCTCCTAAATA	4542
rs536075201	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8523318	GATTACAGGCATGAG[C/T]CACCGCGCCTGGCCA	4542
rs536077076	snp	C/T	0	0	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530059	GCAGGTGCATATGGG[C/T]CAGGTGAGGGTGTAC	4542
rs536156539	snp	C/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8562425	CAATCCTCCTGCCTT[C/G]ACCTCCTGAGTAGCT	4542
rs536178572	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8545519	TGGTTGTTATCTGTC[A/G]CTGGAAGTCCTGAGT	4542
rs536197936	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8552687	AAACTCAGGAAGTTG[C/T]ATAGATTTTTTTCCC	4542
rs536199759	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8546454	AACCTTGACCTCCAG[A/G]GTTCAAGTGATCCTC	4542
rs536230105	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8575318	TTGACTTCGTGATCT[C/G]CCCGCCTCGGCCTCC	4542
rs536294583	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8573716	TTAGCTGGGTGTGGT[A/G]GCAGGTGCTTGTAAT	4542
rs536365720	in-del	-/CAG	0.00716266	0.059414	intron-variant	MYO1F	GRCh38.p7	19:8552940	GTGTCATGGCCTCCA[-/CAG]CAGTTCTGCCAATGG	4542
rs536425893	snp	G/T	0.00358779	0.0422022	intron-variant	MYO1F	GRCh38.p7	19:8570609	TGACCCCAAGTGATC[G/T]GCCCGCCTTGACCTC	4542
rs536451712	snp	A/C	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8569699	TTCCTGTAGAAGGCA[A/C]GTCTTGCAACATGAA	4542
rs536544284	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8543202	AGCCACCACTCCCAG[A/C]CTCTCCAGCCCATTT	4542
rs536554084	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8536807	TCCCTTCTGGGGTCA[C/G]TTCTGCAGGTGGGGG	4542
rs536579884	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8557887	CACTGCTGCCAGGCC[C/T]CTTCCTTCTCCCTCC	4542
rs536587355	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8571319	CTGGGGCCACACCCT[C/G]CGTCCATGCACTGTG	4542
rs536589234	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8564018	TTTTGAAACTATGGG[A/G]GTTGAGTGTGTCCAT	4542
rs536687910	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8539491	ATCCCAGCTACTTAG[A/G]AGGCTGAGGCAGAAG	4542
rs536712818	snp	A/T	0.0162398	0.0886349	intron-variant	MYO1F	GRCh38.p7	19:8534178	AGCGAGACTCTGTCT[A/T]AAAAAAAAAAAAAAA	4542
rs536735445	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8541751	TTACTTTTTACATCA[C/G]AACTAGTCCATAGAA	4542
rs536818239	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8562138	CTCCAGGGTTCACGC[C/T]GTTCTCCTGCCCGGC	4542
rs536856973	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8568492	GAGGGTTTTGCTCAA[A/G]TGAATATCGTGTGGG	4542
rs536875197	snp	C/G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8535068	AGGTGTGCACCACCA[C/G/T]GCCCAGCTAATTTTT	4542
rs536875277	snp	C/T	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8528593	AAAACAAAAAAGAAA[C/T]GAGGTCAGATGGGAA	4542
rs536899062	snp	A/G	3.35093e-05	0.0040931	synonymous-codon, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536339	AAGCAGGTGCTGGAC[A/G]CCCTGGCGTTCGTCC	4542
rs536981713	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8537790	GCTGGGGTATAGTGG[C/T]GCCGTGATAGTTCAC	4542
rs537008200	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8557765	TTGGTGGGAAGTGGG[C/T]GCATCCCAGTTCTCA	4542
rs537173637	snp	A/G	1.65655e-05	0.00287793	intron-variant	MYO1F	GRCh38.p7	19:8552029	CCCGGCCCCTTCCCT[A/G]CACCTGGTAGTAGAT	4542
rs537183845	snp	C/T	0.00318978	0.0398085	intron-variant	MYO1F	GRCh38.p7	19:8574685	TCTTTCTTTCTTTCT[C/T]CCTTTCTCTTTCTCT	4542
rs537245209	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8529361	GCCAAGTCTGGGTGT[A/G]CCTGTGGACAGGAGA	4542
rs537252555	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8575171	AACCTCCGCCTCCCG[A/G]GTTCAAGCGATTCTC	4542
rs537386325	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8569883	TGCTGGCCTCTCATT[A/G]CTTAGGAGGACAGGA	4542
rs537556304	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8570627	CCGCCTTGACCTCCC[A/G]AAGTGCTGGAATGAC	4542
rs537662887	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	MYO1F	GRCh38.p7	19:8520933	CCCAGCCCAAACTGG[G/T]ACAAATTCAAGCTTT	4542
rs537703401	snp	C/T	6.63559e-05	0.00575965	missense, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530210	CCTTGAAGCGGCGGT[C/T]GTACTTGGTGACCGA	4542
rs537740249	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8535823	TAGCTGGGACCACAG[A/G]TGCCCGCCACCATGC	4542
rs537795249	snp	A/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8562136	GCCTCCAGGGTTCAC[A/G]CCGTTCTCCTGCCCG	4542
rs537797113	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8543840	GTGGTGGTGGTGGTG[C/G]TGGTGGTGGTGGTGG	4542
rs537835807	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8524362	TGGAAAGTTGCAGTG[C/T]GCTGAGACCGCACCA	4542
rs537851986	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8570453	CTTGGCTCAACCTCT[A/G]CCTCCCAGGTTCAAG	4542
rs537889968	snp	A/T	0.0023933	0.0345097	intron-variant	MYO1F	GRCh38.p7	19:8542773	ACCTGGCTGATTTTT[A/T]TTTTTATTTTTAATA	4542
rs537913931	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8531716	AACGGTATGATGTCA[C/T]GGTTTCTTACACTGT	4542
rs537929066	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8552846	AGGAATGGATGAGGG[A/C]ATAAATTGGACCTGA	4542
rs537929145	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8559382	GATCAGATTCTGGAC[A/C]TACTGACAGTTAGAG	4542
rs537949299	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8537380	ACAGAGCCCTTATGA[A/G]AGCATTTCTTTTTGT	4542
rs537987379	snp	C/T	1.72136e-05	0.00293369	missense	MYO1F	GRCh38.p7	19:8522478	CTGGGACCATGTGTC[C/T]GAGGCTGGGGCTTGG	4542
rs538002893	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8556779	GTTATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	4542
rs538076461	snp	C/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8532010	GTCATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	4542
rs538111120	snp	A/G	0.00517822	0.0506191	intron-variant	MYO1F	GRCh38.p7	19:8522172	GGACTACAGGCGCCC[A/G]CCACCACGCCCGGCT	4542
rs538120102	snp	G/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8542301	CAGCTTGCATCAGAG[G/T]CCGGGGGGCGGTGAA	4542
rs538137944	snp	A/T	1.65649e-05	0.00287788	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554676	TGATAGAGGTCGATC[A/T]CACGGTCGGTGAAGT	4542
rs538165561	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8555356	GCCTGGAACCTGGGC[A/G]ACAGAGCAAGACTCC	4542
rs538166203	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8547893	GAAGGAAGTATCACT[A/G]TGGAGCCTGGGTAGG	4542
rs538184457	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8560533	TGCCTCTGTCTACAC[A/G]CACAGGAGGCTGGGC	4542
rs538212503	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8523419	ACAATCGTAGCTCAC[C/T]GCAACTCTGACCTCC	4542
rs538222189	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578180	GTCTAGCTCTGTCAC[C/G]CAGGCTAGAATGCAG	4542
rs538318695	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8523830	CAGCTAATTTAAAAA[G/T]AATTTTTAGGCTAGG	4542
rs538419341	snp	C/T	0.00279162	0.0372561	intron-variant	MYO1F	GRCh38.p7	19:8523100	GCAGTGGCGCGATCT[C/T]GGCTCACTGCAAGCT	4542
rs538425463	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8521722	GGCTGGTCTTAAACT[A/C]CTAGGCTTAAGCCAT	4542
rs538460019	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8525782	TGGGCCCGCCCACTT[G/T]AGGTCACTCCTTCAT	4542
rs538489296	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8549107	AGGCATGCGCCACCA[C/T]GCCCGGCTAATTCTT	4542
rs538538380	snp	C/T	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8553407	CATGATATATTTGGC[C/T]GCCACTGTCTTCCCA	4542
rs538574971	snp	A/T			intron-variant	MYO1F	GRCh38.p7	19:8567203	TCTCGAGTAGCTGGG[A/T]TTATAGGCACCCACC	4542
rs538703065	snp	C/G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8547796	GCACCCTAAACAGTA[C/G/T]CTGGCACACAACAGG	4542
rs538732083	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8563738	GCTGGTCTGGAACTC[C/G]TGACCTCAGGCGATC	4542
rs538735247	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530122	ATATCTGGCTGTGGG[A/C]AGGTGCATCTGGGCC	4542
rs538752469	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8542168	TCAGAATAGGGGATG[C/G]GGGGCGGGCTTCCTG	4542
rs538769857	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8563240	TCAGGTGATCCACCC[A/G]CCTCGGCCTCCCAAA	4542
rs538867334	snp	A/C	0.11963	0.213316	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578066	AAAAAACCAAAAAAA[A/C]AACAACAACAGGGAA	4542
rs538876705	snp	A/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8537276	TCTGCCTGACCCTGG[A/T]ACCCAAGACAAGGAG	4542
rs538916583	snp	C/T	0.00199481	0.0315187	intron-variant	MYO1F	GRCh38.p7	19:8525682	GCTCTCCCATTAGCA[C/T]CGCCCCTTAGGTACA	4542
rs538983038	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8565151	ATCCACCCACCTCAG[A/C]CTCCCAAAGTGCTGG	4542
rs538983044	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8559623	CCAAGCCTGAGTGGT[C/T]GTGAGGATAGACCGA	4542
rs539005191	snp	A/G	0.00279162	0.0372561	intron-variant	MYO1F	GRCh38.p7	19:8560506	AAGGAAAAAAAAAAA[A/G]GAACAGGTTCTTGCC	4542
rs539022574	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8577233	CCAATTTCTGATGGT[C/T]ATTTTTAGGACACCT	4542
rs539144601	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8548884	TGAGCCACTGCGCCC[A/G]GCCTTGCACCTCTAT	4542
rs539167590	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8577519	AAGCTGGGTGTGGAG[G/T]GGGGCGGGGAGCTGG	4542
rs539229901	snp	C/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8571359	TTCTCACCTCCAAAG[C/G]CTCCATCCCTCAGGG	4542
rs539332383	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8543969	GTGGTGGTGGTGGTG[A/G]TGCTGGTGCTGGTGC	4542
rs539351473	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8531017	CCATTGCACTCCAGC[C/G]TGGACAACAAGAGTG	4542
rs539379757	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8554214	CTCTCGCCTTGGCCT[C/G]CCAAAGTGCCAGGAT	4542
rs539437280	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8522142	ATTCTCCTGCCTCAG[C/T]CTCCCGAGTAGCTGG	4542
rs539458149	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8573078	CTTTGGGAGGCTGAG[G/T]CGGGCAGATCACGAG	4542
rs539480403	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8532743	CTAAGCAAAAATTAG[C/T]TGAGGGTGATGGCAC	4542
rs539518897	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8542984	TCTTGGCTTACTGCA[A/G]CCTCCACCTCTTGGA	4542
rs539541834	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8548536	AAGTGTCAGTGTATC[A/G]GGGTCCCTGACTCCA	4542
rs539685143	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8544140	TAGTTCTGGTTAGTA[C/G]GGGGTGGATTGAGGC	4542
rs539686166	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8532086	TTGCGCCACTGCACT[C/G]CAGCCTGGGCGACAG	4542
rs539711362	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8538730	GTAGCTGGGACCACA[C/G]GTGTGCACTACTATG	4542
rs539721409	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8545074	TGAGCCACCATGTCC[C/T]GCCTAAATACGTCTT	4542
rs539724789	snp	A/G	0.000155568	0.00881814	intron-variant	MYO1F	GRCh38.p7	19:8544497	GCCAGCAGCGGCTCA[A/G]TTTGGTCTGCCTTGC	4542
rs539773744	snp	A/T			intron-variant	MYO1F	GRCh38.p7	19:8523678	TATTTGTTTAGAGAC[A/T]GGGTTTTGCTCTGTG	4542
rs539815594	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8552952	TCCACAGTTCTGCCA[A/G]TGGGGGACTCTCTTT	4542
rs539831155	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8566270	CCTCCCGGGTTCACG[C/G]CATTCTCCTGCCTCA	4542
rs539851234	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8558726	TAAGATGTCTCTCCT[C/T]CTGGAAGCCCCCCAT	4542
rs539876225	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8527829	TGTTGCCCAGGCTGG[G/T]CTTGAGCTCCTGATC	4542
rs539939032	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8555355	AGCCTGGAACCTGGG[C/T]GACAGAGCAAGACTC	4542
rs539939083	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8561490	TTTTTCTCTTTCTTT[C/T]GTTCTCTTTCTTCTC	4542
rs539982724	snp	A/G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8571260	AGACCCTGCCCTGGT[A/G/T]CCTGAGGGTGGCCCT	4542
rs540143138	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8558118	GCCAGCACCTTCTTA[G/T]GTTGCCATTTTTTTC	4542
rs540158235	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8530985	GGAGGCGGAGGTTGC[A/G]GTGAGCTGAGATCGC	4542
rs540164465	snp	A/G	0.00358779	0.0422022	intron-variant	MYO1F	GRCh38.p7	19:8560442	GTGAGCCGAGATTGC[A/G]CCATTGCACTCCAAC	4542
rs540202839	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8546700	TTCTTTTTTGAGACA[A/G]GGTCTCATTCTGCTG	4542
rs540276107	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8525310	GAAGGGCTCTGAATG[A/C]CAAACTAAGTTTAGC	4542
rs540304102	snp	A/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8521817	TACTCTTTAAAAGTT[A/T]TTTTTTTGTAAATCT	4542
rs540321460	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8525186	GCCTGGGAGACAGAG[C/T]TGGACTCCATCTCAA	4542
rs540327863	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8543852	GTGGTGGTGGTGGTG[A/G]TGGTGCTGGTGGTGC	4542
rs540336861	snp	C/T	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8525940	CTCTGGTCCAGCCTG[C/T]TGGCCCCGCCCCACT	4542
rs540384522	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8548669	GCAGTGGCATGATCT[C/T]GGCTCACTGCAAGCT	4542
rs540386209	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8542340	CTCAGATTGGTGGGT[C/G]GGGGGCTGCAGCCTG	4542
rs540414125	snp	A/G	0.00517822	0.0506191	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578016	CCTGGGCGAAAGAGT[A/G]AGACCCTGTCTCTAA	4542
rs540414822	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8571181	ACCCAGGTCCTGCGA[A/G]CTGTGGTTGCCGGGA	4542
rs540543109	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8560212	GTTCTTGGCTGGGCG[C/T]GGTGGCTCACGCCTG	4542
rs540544296	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8549039	CACTGAAACCTCTGC[A/C]TCCAGGATTCAAGAG	4542
rs540551380	snp	A/T			intron-variant	MYO1F	GRCh38.p7	19:8566085	GCACTCCAGCCTGGA[A/T]GACAGACGAAGACCC	4542
rs540582566	snp	C/T	0.00438332	0.0466095	intron-variant	MYO1F	GRCh38.p7	19:8571571	AGGCGCCCGCCACCG[C/T]GCCCGGCTAATTTTT	4542
rs540599977	snp	C/G/T			utr-variant-3-prime	MYO1F	GRCh38.p7	19:8521218	ACTTTGCCAACAGCA[C/G/T]AGGACTCAAGACCCA	4542
rs540637376	snp	A/C	0.0023933	0.0345097	intron-variant	MYO1F	GRCh38.p7	19:8525092	GTAATCTCAGCTACT[A/C]GGGAGGCTGAGGCAG	4542
rs540656874	snp	A/G	0.00199481	0.0315187	intron-variant	MYO1F	GRCh38.p7	19:8572674	AGCAGCCACTTCACT[A/G]GTCTCCCTGCTTTGT	4542
rs540770886	snp	A/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8566481	CTGGTCTATGCTTTT[A/T]AAAAAAAATTTTATT	4542
rs540790499	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8532304	AGAAAAGGGTTTTGA[A/G]TTGTAAAAGTCTAGA	4542
rs540834115	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8567035	ACACACGCTGGCTGA[A/G]GTTAGTCCTATCACT	4542
rs540878326	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578646	CCCCCAGCAGAGCCT[A/G]GCCCAGGTACGTGTC	4542
rs541058231	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8569355	GGGTGGGGTAGGAAG[A/G]ACGGGTAGCTTCTTC	4542
rs541170367	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8573193	GCGGGCGCCTGTAGT[C/G]CCAGCTACTCGGGAG	4542
rs541274120	snp	A/G	0.000208703	0.0102131	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8527483	AGTCCCGCTTGATGG[A/G]CTGTGGGGATGCAGG	4542
rs541274339	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8522257	TCGATCTCCTGACCT[C/T]GTGATCTGCCCGCCT	4542
rs541284889	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8574350	GAATCCAGAAATGAA[C/T]GGACATCCCAGCTAA	4542
rs541294738	snp	A/G	0.000208935	0.0102188	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544414	TCCCCCGCCCGTGGC[A/G]TGCATGGTGGCGCAC	4542
rs541374377	snp	C/G	0.00514076	0.0504376	intron-variant	MYO1F	GRCh38.p7	19:8550551	CAGCCCTCCCTGATA[C/G]CCACACTCACGGTCC	4542
rs541384191	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8521657	GCCCTGGAGAAAGCT[C/T]TCATGCCTGGTCTGT	4542
rs541501176	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8563028	ACCGAGTCTCACTCT[C/G]TCGCCCAGGCTGGAG	4542
rs541555253	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8545195	TGGGCTCAAGTGATC[C/T]TCCCACCTCAGCCTT	4542
rs541596858	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8574902	CTGGGGTTACAGGCG[C/T]GCACCACCACGACTG	4542
rs541624673	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8568151	AGGCTGGGCCGGGCA[C/T]GGTGGCTCACACCTG	4542
rs541676721	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8528930	CCGGTTGAGCTGGCC[G/T]GCGGTCAGAGTTCTC	4542
rs541701214	in-del	-/C	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8540535	ACCAACATGGTGAAA[-/C]CCTGTCTCTACTAAA	4542
rs541714659	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8534454	CTGGGATTACAGGCA[C/T]GTGTCACCATGCCCG	4542
rs541729758	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8522232	TTTCACTGTGTTAGC[C/T]AGGATGGTCTCGATC	4542
rs541801657	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8560780	GTCTTGCTCTGTCGC[C/G]CAGGCTGGAGCGCAG	4542
rs541921735	snp	A/G	0.000118133	0.00768458	utr-variant-5-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8577434	TTCACCGGACTCCCG[A/G]CTTTAGTTCCTCTTA	4542
rs541923003	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8557076	GGACTGCTTAAGGCC[A/G]GCAGTTCAAGACCAG	4542
rs541954811	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8544716	GCAGAAGTGGGTGGG[A/G]ACCCCTCAAGAGATT	4542
rs542025095	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8565648	GAGTGGTGAGGGTCT[A/G]TTCTTTTTCTAAACA	4542
rs542095117	snp	A/C	0.00358779	0.0422022	intron-variant	MYO1F	GRCh38.p7	19:8526117	GTGGAGCATGAGGTA[A/C]TGAGTTCAAGACCAG	4542
rs542097693	snp	A/G	0.000364353	0.0134924	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8548273	AATGTCCAGCACACC[A/G]ATGCTGTACTCTTCC	4542
rs542154853	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526712	CCGAAGCGCAGTTCG[C/G]CCGGGTCGGTGGGGC	4542
rs542211480	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8561038	CACTGCGCCTGGCCA[C/T]GCCTGGCTAATTTTT	4542
rs542211918	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8555447	GGGGGAAATGGAACA[C/T]GCTGGGGCTGAGCTT	4542
rs542264964	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8528153	CTTGAACCCAGGAGG[A/G]TGAGGTTGCAGTGAG	4542
rs542364324	snp	G/T	0.00795532	0.062565	intron-variant	MYO1F	GRCh38.p7	19:8523050	CTTTTTTTTTTTTTT[G/T]AGATGGAGTCTTGCT	4542
rs542396481	in-del	-/CCTT			downstream-variant-500B	MYO1F	GRCh38.p7	19:8520609	CTCCCTCCCTCCCTC[-/CCTT]CCTTCCTTTCTTTTT	4542
rs542400904	snp	C/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8555993	ACTGCTCGGATCCAG[C/G]CCTCAGCCCTCTATT	4542
rs542410879	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8544006	TGGTGCTGGTGGTGG[C/T]GGTGGCGGTGGCGGT	4542
rs542508436	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8546029	TTGTCCACAGCATAA[C/T]GTGCTCATTAACACA	4542
rs542533213	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8539616	AAAAAATTATTGGAT[A/G]TTATTAAGATGATAA	4542
rs542542412	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8543717	GTGGTGCTGGTGGTG[C/G]TGGTGGTGCTGGTGG	4542
rs542542861	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8551504	TTACAGTCACACGCC[A/G]CCACATCTGGCTAAT	4542
rs542724579	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8529329	TGGCCCGCCCAGGTA[C/T]AGGTGACGGTAAACA	4542
rs542738441	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8535894	CACTGTGTTAGCCAG[A/G]ATGGTCTCGATCTCC	4542
rs542748459	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8562169	TAATTTTTTCTTTTT[C/T]TTTTTGTATTTTTAG	4542
rs542760259	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8569530	GGAGGGAACACACTT[C/T]CTGGGCCCCTACTGT	4542
rs542802037	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8576219	GGCCAGGCTGGTCTC[A/G]AACACCTGACCTCAA	4542
rs542821692	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8570050	TAGCTGGGACCACAG[A/G]TGCATACTACCACGC	4542
rs542861489	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8562844	TGGCCAAGTTAAACA[C/T]TTTGGAAACTCACTT	4542
rs542923945	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8543867	GTGGTGCTGGTGGTG[C/G]TGGTGGTGCTGGTGG	4542
rs542989797	snp	A/C	0.0023933	0.0345097	intron-variant	MYO1F	GRCh38.p7	19:8558427	CACCTCAGCCTCCCA[A/C]AGTGCTGGAATTTCA	4542
rs542991850	snp	C/T	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8575509	CTCGGGCTTGCTTGC[C/T]TGCCACTCATCTCCT	4542
rs543052285	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8533038	CTAAGAGCCTTGCTC[C/T]CTGCTCTGCTGACCA	4542
rs543056751	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8550837	TCAGTCACTTGCCGC[A/G]TGACCTTGGGTAAGT	4542
rs543058374	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8573304	TGACAGAGCGAGACT[A/C]TGTCTCAAAAAAAAA	4542
rs543126638	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8535392	TTTGTCTAAATTAAA[C/T]TTTACTTTATATAGT	4542
rs543126900	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8529784	TTGATGGACAGCTGT[A/G]TCTGCTATACTTGAG	4542
rs543152746	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8527596	TGAGGAAGGTGGGAG[C/T]CCTCCAGGTGAAGGT	4542
rs543215763	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8561801	GGCTCACTGCAAAAT[C/G]TACCTCCCAGGTTCA	4542
rs543262761	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8552786	TTCACTGGGCCCAGC[A/G]CAGCACCCACACAAA	4542
rs543288042	snp	A/C	3.31532e-05	0.0040713	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530429	GGTCCTTGTGCCCCC[A/C]CCCCGCGCCGTTTAC	4542
rs543292311	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8523392	CTCTCGCCCAGGTTG[C/G]AGTGCAGTGGTACAA	4542
rs543337294	snp	G/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8552392	GCCTCCTGAGTAGCT[G/T]GGACTACAGGCACCC	4542
rs543355028	snp	A/C	0.00636936	0.0560724	intron-variant	MYO1F	GRCh38.p7	19:8523922	TCTGGAGTTTGAGAC[A/C]AGCCTGGCCAACATA	4542
rs543376626	snp	A/G	0.000298166	0.0122063	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550593	TCGGGCGTAATTCCC[A/G]TCTTCACAGAAACTG	4542
rs543384131	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8574132	AATTTCCAGCTGAAA[A/G]CAATCCACCACCAAC	4542
rs543411148	snp	A/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8534761	CTCCTGAGTAGCTGG[A/G]ATTACAGGTGCGCAC	4542
rs543450885	in-del	-/T			intron-variant	MYO1F	GRCh38.p7	19:8535685	CACATTCTTTCTTTC[-/T]TTTTTTTTTTTTGAG	4542
rs543467942	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8528104	GTGGGCACCTGTAGT[C/T]CCAGCTACTCAGGAG	4542
rs543490570	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8541620	TTTTAGTAGAGACAA[A/G]GTTTTGCCATGTTGC	4542
rs543527162	snp	C/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8540535	ACCAACATGGTGAAA[C/T]CCTGTCTCTACTAAA	4542
rs543627719	snp	A/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8575473	CTAATGGCGCCCCCG[A/G]GAATCTGAGAGGAGG	4542
rs543698652	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8528961	TGGGTCTAGTGGGGA[C/T]ACCTGTCTCAGTGAA	4542
rs543750031	snp	A/G	1.65603e-05	0.00287747	synonymous-codon, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8545662	CACCAGCTTGTTTTC[A/G]ATGAGGTCACAGACG	4542
rs543866562	snp	C/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8563390	GCAACCTCTGCTTCC[C/T]GGATTCAAGCGATTC	4542
rs543912352	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8534680	GCCCAGGCTAGAGTG[C/T]AGTGGTGCGATCTCG	4542
rs543913969	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8568095	GCCCCAGGCACTAGA[A/G]GCCCTCAGACACTCC	4542
rs543992470	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8537848	GATCAACTGCCTTAG[C/T]CTCCGGAGTAGCTAG	4542
rs544004665	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8558933	AGGCTGGATGGAGTG[C/T]AGTGGTGAGACCACG	4542
rs544028190	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8547208	TGAGAGGCTGAAGTG[G/T]GAGGATTGCTTGAGC	4542
rs544070733	snp	C/T	0.0023933	0.0345097	intron-variant	MYO1F	GRCh38.p7	19:8564841	GCAGTGGTATGATTT[C/T]GGCTCACTGCAACCT	4542
rs544098232	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8529740	GTGAGGGTGTATCTG[A/G]CAGGTGTGTCTGGGC	4542
rs544132838	snp	A/G	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8562769	TAACTCCTGGGCTCA[A/G]GCAATCCTCCTGCCT	4542
rs544192428	snp	A/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8551674	GGTTTCCTAATTTGT[A/T]ACTCAGGAGGGTTTC	4542
rs544205106	snp	G/T	8.38118e-05	0.00647293	intron-variant	MYO1F	GRCh38.p7	19:8541864	TCCCTCCATCCCCTT[G/T]GGGGGTTGTAGCCGG	4542
rs544230580	snp	C/T	0.00398564	0.0444627	intron-variant	MYO1F	GRCh38.p7	19:8557373	GTGATCACAGCTCCA[C/T]GCAGCCTCAACCTCC	4542
rs544305028	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8559672	AGAATTAACACGACC[C/G]GGCGCGGTGGCTCAC	4542
rs544343685	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8543545	TGTTAATCGGGGGGA[A/G]TTCTGTTCCCTCTGT	4542
rs544345306	snp	C/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8525199	AGTTGGACTCCATCT[C/T]AAAAAAAAAAAAAAA	4542
rs544379412	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8557829	ATCCCCCGTCCCCTC[C/G]CCAGGCCCAGGCCAG	4542
rs544440985	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8571110	CTGCTTTTTCTGGGC[A/G]TGATGAGCAAGAGCT	4542
rs544469178	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8577252	TTTAGGACACCTCCA[C/G]CTGGCTGGTGTCCCT	4542
rs544483780	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8552738	AGTGATAGAATCAAA[C/T]CCTGAATCCATATCT	4542
rs544493797	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8548587	CCTCTCTGCACCTCT[A/G]TTTTCTTTTTTTTTT	4542
rs544499784	snp	A/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8575780	GACCTTGTCTGCCAA[A/G]CCGACTGTTGACTAA	4542
rs544506974	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	MYO1F	GRCh38.p7	19:8521253	TTAATCACATGGCAG[C/T]TGGGAGGTAGATTCT	4542
rs544515400	snp	A/G			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8577992	CCTGATTGCGCCACT[A/G]CACTCCAGCCTGGGC	4542
rs544532659	snp	A/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8554281	ATTTAGAGGGGACAG[A/T]CAGACAATAGCAGAA	4542
rs544630368	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8571006	TGCTAGCGTTCCTCA[C/T]TGTCCCCATCAATGG	4542
rs544632823	snp	A/T	0.00279162	0.0372561	intron-variant	MYO1F	GRCh38.p7	19:8523248	TCATGTTAGCCAGGA[A/T]GGTCTCGATCTCCTG	4542
rs544651859	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8556714	TCAATATGGAGAAAC[A/C]CCGTCTATACTAAAA	4542
rs544664620	snp	C/T	0.0023933	0.0345097	downstream-variant-500B	MYO1F	GRCh38.p7	19:8520706	GCAGCCTCTGCCTCC[C/T]GGGTTCAAGTGATTC	4542
rs544897982	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8544024	TGGCGGTGGCGGTGG[C/T]GGTGGCGGTGGCGGT	4542
rs544918691	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8540662	TTGCAGTGAGCCGAG[A/G]TCGTGCCACTGCACT	4542
rs544954537	snp	G/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8535416	ATATAGTCTTTGCTG[G/T]TGATAGTTATTTTTC	4542
rs544959527	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8543886	TGGTGCTGGTGGTGG[C/T]GGTGGTGGTGCTGGT	4542
rs544994802	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8562631	GCCTTGACGTCCAGG[A/C]TCAAGTGATCCTCCC	4542
rs545033086	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8562192	ATTTTTAGTGGAGAC[A/G]AGGTTTCACCGTGTT	4542
rs545071118	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8575321	ACTTCGTGATCTGCC[C/T]GCCTCGGCCTCCCAA	4542
rs545084067	snp	C/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8551553	GACGGGGTTTAACCA[C/T]GTTGGCCAGGCCGGT	4542
rs545117870	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8561820	CTCCCAGGTTCAAAC[A/G]ATTCTTCTGCCTCAG	4542
rs545139124	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8530733	TTTCTAGTGACACTC[A/G]TTCATAAAGAAAAGA	4542
rs545146409	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8563548	AGTGTCTCTCTTGTT[A/G]TCTGGGCTGGAGTGC	4542
rs545157244	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8557322	AAAGTTTTGAGACAG[C/G]GTCTCACTCTGTCAC	4542
rs545207577	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8558413	TCAAGTGATCCTCCC[A/G]CCTCAGCCTCCCAAA	4542
rs545216954	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8570761	GATCCTCTTGCCTTG[A/G]CCTCCCAAAGCGCTG	4542
rs545302738	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8524522	CCCAGGAGGTGGATG[C/T]TGCAGTGAGCCAAGA	4542
rs545369483	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8570150	TGATCTAGGCTTACT[A/G]CAACCTCTGCCTCCC	4542
rs545375534	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8553647	GGAGCCTGAGGAGGG[C/T]GGATCACTTGAGGTC	4542
rs545482627	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8523948	ACATAGTGAAACTCT[A/G]CCTCTACTAAAAATA	4542
rs545565665	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8573666	ACCAGCCTGGCCAAC[A/G]TGGCGAAACCCCGTC	4542
rs545578361	in-del	-/AA	0.0178098	0.0926698	intron-variant	MYO1F	GRCh38.p7	19:8532889	GAGATCCTGTCTCAG[-/AA]AAAAAAAAAAAAATA	4542
rs545607474	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	MYO1F	GRCh38.p7	19:8520451	GGCGCCCGCCACCAC[A/G]CCCGGCTACTTTTTT	4542
rs545780864	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8522213	ATTTTTAGTAGAGAC[A/G]GGGTTTCACTGTGTT	4542
rs545956753	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8564805	TGAGACAGAGTCTCG[C/T]TCTGTCACCCAGGCT	4542
rs546018190	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8531339	GCAACAAGAGCAAAA[C/T]TTCATCTCAAAAAAA	4542
rs546033371	snp	C/T	0.000289069	0.0120188	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544366	GTGGGTCCCCACAGC[C/T]GCCTGCAGCTTCTGC	4542
rs546062679	snp	C/T	0.00199481	0.0315187	intron-variant	MYO1F	GRCh38.p7	19:8537641	GTTTTGCCATGTTGG[C/T]CAGGCTGGTCATGAA	4542
rs546065783	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8532544	ATCCTACTTCAAAGA[A/G]AAACTGTGATCAAAG	4542
rs546205140	snp	C/T	0.00597247	0.0543191	intron-variant	MYO1F	GRCh38.p7	19:8541577	GGAATTACAGGTGCG[C/T]GCCACCACGCCTAGG	4542
rs546229539	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8560356	CGGGTGTGGGGGTGC[A/G]CGCCTGTAATCCCAG	4542
rs546338727	snp	A/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8549785	GCTGGGATTACAGGC[A/G]TGAGCCACTGCATCT	4542
rs546347485	snp	C/T	1.68168e-05	0.00289967	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8530547	GCCATCGAACTTTCG[C/T]TCTCGCACCTCCTCC	4542
rs546530769	snp	C/T	0.00318978	0.0398085	intron-variant	MYO1F	GRCh38.p7	19:8540789	CGTCATGGATTGAGA[C/T]ACTGCTTAAAGTGGG	4542
rs546569876	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8575886	CAAAGCCCTGCCCAT[A/C]CCAGGACCTGAGCCT	4542
rs546683817	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8559160	GCTGGGATTACAGGC[A/G]TGAGCCACCGCTCCC	4542
rs546684512	snp	C/T	0.000231865	0.0107647	intron-variant	MYO1F	GRCh38.p7	19:8548206	CTGCCCCAGGGAGGA[C/T]AGGATGTGGGCTGGA	4542
rs546692161	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8535719	GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC	4542
rs546723257	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8547640	TGACTTACTTCCTCA[A/G]TCTCCTCTTGGAGCT	4542
rs546726295	snp	C/T	0.000798403	0.0199641	downstream-variant-500B	MYO1F	GRCh38.p7	19:8520774	AGGCACCACCACACC[C/T]GGCTTTTTTTTTTTT	4542
rs546745623	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8542734	GCCTCCCGATGAGCT[G/T]GGATTACAGGCGTGT	4542
rs546841847	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8570382	GCCACATTTTTTTTT[G/T]TATTTGAGATGGAGT	4542
rs546873570	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578007	GCACTCCAGCCTGGG[C/T]GAAAGAGTGAGACCC	4542
rs546918154	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8558629	CTCTGTCTCTATTCA[A/G]CACATCTCTGCAAAG	4542
rs546930028	snp	A/G	0.00478085	0.0486577	intron-variant	MYO1F	GRCh38.p7	19:8522229	GGGTTTCACTGTGTT[A/G]GCCAGGATGGTCTCG	4542
rs546957250	snp	A/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8531559	GCCCAGGCTGGAAAA[A/T]TTTTTATCTTCCTCC	4542
rs546960767	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8564253	AGGCGTGGTGTCAGG[C/T]GCCTGTAATCCCAGC	4542
rs547013077	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8564976	CAGGATTTCACCACG[C/T]TGGACACGCTCATCT	4542
rs547021858	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8556563	ATGAAAAGACATGGA[A/G]GAAACTTAAAGGCAT	4542
rs547082756	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8576173	AGTTAATTTTTTGTA[C/T]TTTTTAGTAGAGACG	4542
rs547125531	snp	A/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8536826	TGCAGGTGGGGGATT[A/G]TGGGAGGGGCTGTGC	4542
rs547256756	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8523181	GGACTACAGGCACCT[A/G]CCACCACGCCTGGAT	4542
rs547389594	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8572237	TCTGATTCATTGTTA[C/T]GTTCACTCTTTGCAT	4542
rs547412123	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8531905	GGCGGATCACCTGAG[A/G]TCAAGAGTTTGAGAC	4542
rs547434815	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8563945	TGACCCTAGCACTCT[C/T]ATATTTGGACACACA	4542
rs547509044	snp	C/T	1.65754e-05	0.00287879	synonymous-codon, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530238	CGAATCGGCGAAGTC[C/T]ACCCGCTCCCTCTTG	4542
rs547516698	snp	A/G	1.6886e-05	0.00290564	synonymous-codon	MYO1F	GRCh38.p7	19:8521543	TCAGATCTTCTCCAC[A/G]TAGTTTCCTGGGAAA	4542
rs547539929	snp	C/T	0.00597247	0.0543191	intron-variant	MYO1F	GRCh38.p7	19:8555068	TGCATGCCTGTAATC[C/T]CGGCTACTTGGGAGG	4542
rs547548393	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8543892	TGGTGGTGGTGGTGG[C/T]GGTGCTGGTGGTGGT	4542
rs547587415	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8548840	TGATCCGCCCGCCTC[A/G]GCCTCCCAAAGTGCC	4542
rs547685891	snp	C/T	6.91073e-05	0.00587783	synonymous-codon	MYO1F	GRCh38.p7	19:8522687	GTTGTGCTCTGAGGG[C/T]GGACGTGCCCGGGGT	4542
rs547704328	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8549387	GGGATTCTTCCACCT[C/T]AGCCTCCTGAGTAGC	4542
rs547705203	snp	A/G	4.38702e-05	0.00468329	intron-variant	MYO1F	GRCh38.p7	19:8544491	GCGGGAGCCAGCAGC[A/G]GCTCAGTTTGGTCTG	4542
rs547712875	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8561956	TCCTGACCTCGTGAT[A/C]CACCCATGTCGGCCT	4542
rs547741787	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8544061	GGTGGTGGTGGTGGT[A/G]GTGGTGGTGTCCAGA	4542
rs547768324	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8538708	TCCTCCTGCCTCAGC[C/T]TCCCAAGTAGCTGGG	4542
rs547808942	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8577966	CCTGGGAGGTGGAGG[C/T]CTCAGTGAGCCCTGA	4542
rs547810207	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8571261	GACCCTGCCCTGGTG[C/T]CTGAGGGTGGCCCTG	4542
rs547825192	snp	A/C/T	3.31588e-05	0.00407167	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555748	CCATGTCATCCACGC[A/C/T]GCTCTGCTTCACGTT	4542
rs547827789	snp	A/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8573503	GCATCAGCCTTCCTT[A/T]CATTCTCCCACGATC	4542
rs547842945	in-del	-/CT	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8529274	TACTGGGCTAGGTGA[-/CT]CTCTGGGACATGAGA	4542
rs547870888	snp	A/G	0.0023933	0.0345097	intron-variant	MYO1F	GRCh38.p7	19:8566761	TCAAGTGATCCACCC[A/G]CCTCAGCCTCCCAAA	4542
rs547931031	snp	G/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8564907	CCTCCCAAGTAACTG[G/T]AATTACAGGCGCCTG	4542
rs548129513	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8537164	GAGACTGGGGGTGGG[C/T]GAGGGCTGGTAACAG	4542
rs548159948	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8564404	ACAAAAAAAGAAGGA[G/T]GTGCTGACTGGGATG	4542
rs548170923	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8531104	TATAATCCCAGCGCC[C/T]TGGGAGGCTGAGGCG	4542
rs548271682	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8532040	GGAGAATCGCTTGAA[C/T]TCGGGAGGTGGTGGT	4542
rs548333398	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8532665	GCTAAGGTGGGAGCA[C/T]TGTTGAGCCCAGGAG	4542
rs548385465	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8553996	GGGTCTCACTCTGTT[A/G]CCCAGGCTGGAGTGC	4542
rs548405965	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8553566	GGATACTGTAATGAA[A/C]AAGACAGATAAAATC	4542
rs548459943	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8527684	GTGGTGCCATCATAG[C/T]TCACTGCAACCTCCC	4542
rs548544617	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8554465	TCTGTGGCCCCCCAA[A/C]TCTGTCCATACCTAA	4542
rs548546595	snp	C/T	0.000185621	0.00963204	intron-variant	MYO1F	GRCh38.p7	19:8548358	TCAGTGGGCATCGGT[C/T]AGATCTGAAGCCCCT	4542
rs548662699	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8572512	ACCTCAAGTGATCCA[C/T]CTGCCTCGGCCTCCT	4542
rs548772581	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8544987	TTCACCATGTTGGCC[A/G]GGCTGGTTTCGAACT	4542
rs548826363	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8550856	CCTTGGGTAAGTGCC[G/T]GCACCTCTCTGGGCT	4542
rs548827078	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8574530	ATTTCTTCTTTTTTC[C/T]CTTTCTTTCTTTCTT	4542
rs548840856	snp	C/T	0.00288157	0.0378481	intron-variant	MYO1F	GRCh38.p7	19:8548011	CACCCCAGGATCCCC[C/T]ATCCCTGACTGCTTG	4542
rs548923265	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8535259	TCTTTTATAAATATT[C/T]AGTCTGTCTTTGTTG	4542
rs548944592	snp	C/T	0.0026537	0.0363292	intron-variant	MYO1F	GRCh38.p7	19:8555600	ACCCTCCTCTCCGTC[C/T]ATGGCCCAGCCATTC	4542
rs548963053	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8563890	CGCCTTGGCTTCTCA[A/G]AGTGCTGAGATTATA	4542
rs548979611	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8561239	CAGTCAGGGTTAACT[A/G]TCTGGGGAAAGGTGT	4542
rs548985202	snp	C/T	0.0185938	0.0946107	intron-variant	MYO1F	GRCh38.p7	19:8568299	GCGGTGGCGGGCGCC[C/T]GTAGTCCCAGCTCCT	4542
rs548988996	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8575040	AGATTACAGGCATGA[A/G]CCACTGCACCCTGCC	4542
rs549007882	snp	A/G	1.73018e-05	0.00294119	missense	MYO1F	GRCh38.p7	19:8522662	GGTCAGGCACGTTGA[A/G]GAATTCTGTGTTGTG	4542
rs549193638	snp	A/T			intron-variant	MYO1F	GRCh38.p7	19:8576428	GCCGCTGTCACAGCC[A/T]CATGCTCTCATCCTC	4542
rs549280140	snp	C/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8557561	TCTGTCTCAGTCCCC[C/G]AAAGTGGTGGGATTA	4542
rs549290759	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8539893	CCGGACCCCAGGTAG[G/T]GTGGAACTCAGCCCT	4542
rs549341007	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8560938	GAGACGGGGTTTCAC[C/T]GTATTAGCCAGGATG	4542
rs549356471	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8528356	ATACCATGAAACCCC[A/G]TCTCTACTAAAAATA	4542
rs549505811	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8555104	GGAGGAGAATCGCTT[C/G]AACCTGGGAGGCAGA	4542
rs549522988	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8523156	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA	4542
rs549560580	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8556945	CTATTTACTGTCTTA[G/T]TCCAACTATAGGATA	4542
rs549610064	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8566956	TGCTAGGATTACAGG[C/T]GTAAGCCACCAGGCC	4542
rs549684150	snp	C/T	4.63456e-05	0.00481359	intron-variant	MYO1F	GRCh38.p7	19:8544504	GCGGCTCAGTTTGGT[C/T]TGCCTTGCCTCCCCA	4542
rs549691073	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8546226	TGTGCCACCACGCCG[A/G]ACTAATTTTGTATTT	4542
rs549712595	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8549484	CATGTTGCCCAGGCT[C/G]ACTCCATACATTAAA	4542
rs549753168	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8574404	CATGTTATGTGCTCT[A/G]TAAAGCAATGGTCCC	4542
rs549764175	snp	A/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8566503	AATTTTATTTTTATT[A/T]ATTTAATTTAATTAA	4542
rs549901204	snp	C/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8567614	CTCCCACCTCGGCCT[C/T]GCAAAGTGCTGGGAT	4542
rs549912115	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8550079	CATTGGGATTGCAGC[C/T]GTGAGCCACTGCACT	4542
rs549991223	snp	A/G	0.000399281	0.0141238	missense	MYO1F	GRCh38.p7	19:8522722	TGCTGGCTCCCAGGG[A/G]TGTGGACGGAGGGCC	4542
rs550020767	snp	C/T			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578806	CGACCCTGGGAGACC[C/T]TGGGGGACCCATGTT	4542
rs550029915	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8527830	GTTGCCCAGGCTGGT[C/T]TTGAGCTCCTGATCT	4542
rs550083266	snp	C/T	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8562247	ACCTCGTTACCCGCC[C/T]GCCTTGGCCTCACAA	4542
rs550085007	snp	A/C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8544830	GCCCAGGCTGGAGAG[A/C/T]AGTGGCGTGATCTCA	4542
rs550099542	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8539306	GTAATCCCAGCTACT[G/T]GGGAGGCTGAGGCAG	4542
rs550160929	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8539833	TCAGAGGCAGAAGCC[C/T]CAGGATTGGTAGACA	4542
rs550205333	snp	C/T	0.0185938	0.0946107	intron-variant	MYO1F	GRCh38.p7	19:8568283	AAAAAATTAGCCAGG[C/T]GCGGTGGCGGGCGCC	4542
rs550233924	snp	G/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8528314	TGGGTGGATCACAAG[G/T]TCAGAAGATTGAGAC	4542
rs550260272	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8535123	CACCATGTTGGCCAG[A/G]CTGGTCTCAAACTCC	4542
rs550321721	snp	G/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8533948	CCAGCACTTTGGGAG[G/T]CTGAGGTGGGCAGAT	4542
rs550323464	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8535563	GCATGCGCTACCACA[C/T]CTGACTTGGTGCTAG	4542
rs550367755	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8562003	TACAGGCATGAGCCA[C/G]TGCGTCTGGCCCTTC	4542
rs550374908	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8556183	ACAGGTGCCCACCAC[C/T]ATGCCCGGCTAATTT	4542
rs550394570	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8530647	TCCGGGTTTTCCCTG[C/T]GCTCACCCTACTCAC	4542
rs550401980	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8540679	CGTGCCACTGCACTC[C/T]AGCCTGGGCGGCAGG	4542
rs550455587	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8543930	GTGGTGGTGGTGGTG[C/G]TGGTGGTGCTGGTGG	4542
rs550523645	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8545897	GTGCCAGGGAATTAC[A/G]TCTGGTTTCAGCAGT	4542
rs550530983	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8569023	GCGCCGAGATGCCTC[A/C]GGAAATGTCATCTGT	4542
rs550553204	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8570227	ACAGGCGTGCACAAC[A/G]CCTGGCTAATTTTTG	4542
rs550598696	snp	G/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8551254	ATGGGGTTTCACTAT[G/T]TTGGCCAGGCTGGTC	4542
rs550643631	in-del	-/G	0.00636936	0.0560724	intron-variant	MYO1F	GRCh38.p7	19:8521955	CCACCTCGCCCATCT[-/G]TTATCTCTGTTCTCC	4542
rs550704180	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8552571	CACACCCAGCCCAAG[C/G]GTATGGAATTTATTA	4542
rs550716007	snp	G/T	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8563683	CCAGCTAATTTTTTT[G/T]GTATTTTTAGTAGAG	4542
rs550741248	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8569636	AGTGGTGTCTCAGTT[A/G]CCCAGAGGAGACCAT	4542
rs550744455	snp	C/T	0.00438332	0.0466095	intron-variant	MYO1F	GRCh38.p7	19:8524075	AGTGAGCCAAGATCA[C/T]GCCACTGCACTCCAG	4542
rs550826890	snp	A/G	0.00225433	0.0334975	utr-variant-5-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8577418	GCCCTGCTTCTGCCC[A/G]TTCACCGGACTCCCG	4542
rs550835762	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8523709	GCCCAGGATGGAGTG[C/T]AGCAGTGAGATCATA	4542
rs551026378	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8542132	CAGTGTCTACAGCGC[G/T]GGCTGGGGGGTATCT	4542
rs551037962	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8574449	CCAGAGACCGGTTTA[A/G]TGGAAGACAATTTTT	4542
rs551051675	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8545822	TCCCCTTCTCCATCT[C/T]ATCACTTAGGACTGT	4542
rs551088499	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8545425	TGAGCTGGGGTTCCC[A/G]GGGAAATGTTTATTG	4542
rs551105039	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8572183	GGGAAGATCCTCTGG[C/G]ATGTGGTCCCCAACC	4542
rs551158736	snp	A/T	0.00358779	0.0422022	intron-variant	MYO1F	GRCh38.p7	19:8547002	TCTCTTTGTTAAAAA[A/T]ATCCCTGTCTCAGGA	4542
rs551293979	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8536742	TCTGTGGTCTGGGGG[A/G]GCTTCGGGGGTCAGC	4542
rs551346484	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8562935	GTTTACAGGTGGGAG[C/T]ACCTGGTGGCTCTCC	4542
rs551382417	in-del	-/T	0.33156	0.236322	intron-variant	MYO1F	GRCh38.p7	19:8563516	TCTTTCTTTCTTTCT[-/T]TTTTTTTTTGAGATG	4542
rs551544369	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8575162	GCTCACTGCAACCTC[C/T]GCCTCCCGGGTTCAA	4542
rs551747359	snp	A/G	2.55771e-05	0.00357602	utr-variant-5-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8577388	CAGGGGGATCTTGGG[A/G]GTGGCTTGGGCATGG	4542
rs551831490	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8535840	GCCCGCCACCATGCC[C/T]GGCTAATTTTTTTTG	4542
rs551869781	in-del	-/TTTTG			intron-variant	MYO1F	GRCh38.p7	19:8537431	TTGGGTGTTTGTTTT[-/TTTTG]TTTTGTTCTGTTTTA	4542
rs551940179	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8571253	AGCTCCCAGACCCTG[C/T]CCTGGTGCCTGAGGG	4542
rs552002430	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8549724	TGGCCAGGCTGGTCT[C/T]AAACTCCAGACCTCA	4542
rs552017240	snp	A/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8568906	AGCCTGGGCAACAGA[A/G]CGAGACTCCATCTCA	4542
rs552091219	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8541635	GGTTTTGCCATGTTG[C/T]CCAGGCTGGTCTCAA	4542
rs552126102	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8524925	TTTGAGGCCAGGCGC[C/T]GTAGCTCATGCTTGT	4542
rs552143488	snp	G/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8570429	AGTCTGTGAGTGCAG[G/T]GGCATGACCTTGGCT	4542
rs552152472	snp	C/T	0.000151336	0.00869741	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8536245	CCTGTCCCTCAAACA[C/T]ACTCACCGACTCTGG	4542
rs552252661	snp	A/G/T	0.00358891	0.0422285	intron-variant	MYO1F	GRCh38.p7	19:8563876	TCAGGTGATCCACCC[A/G/T]CCTTGGCTTCTCAAA	4542
rs552290204	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8542746	GCTGGGATTACAGGC[A/G]TGTGCCACCACACCT	4542
rs552336969	snp	A/G	6.95725e-05	0.00589758	synonymous-codon	MYO1F	GRCh38.p7	19:8522657	GCCCTGGTCAGGCAC[A/G]TTGAGGAATTCTGTG	4542
rs552415383	snp	A/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8564308	ATCGCTTGAACCCAG[A/G]AGGCAGAGGTTGCAG	4542
rs552466417	snp	A/C	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8531954	GAAACCCCGTCTCTA[A/C]TAATAATACAAAAGT	4542
rs552481608	snp	C/T	1.65329e-05	0.0028751	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8553416	TTTGGCTGCCACTGT[C/T]TTCCCAGCTCCACTC	4542
rs552543055	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8547872	CTTCCCAAAGCTTTA[C/G]AGGCAGAAGGAAGTA	4542
rs552544667	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8559822	GGGCGTGGTGGCGCA[C/T]GCCTGTAATCCCAGC	4542
rs552572381	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526300	CCACAACACTCCAGC[C/T]TGGGCGACAGAGTGA	4542
rs552628170	snp	A/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8543422	CTGGGGGCTTTGGGG[A/T]TTTCCTCTCCAAATT	4542
rs552691361	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8531663	CACTAGCTTCAGATC[A/G]CAGCTGTGCCACTTA	4542
rs552727051	snp	C/T	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8575326	GTGATCTGCCCGCCT[C/T]GGCCTCCCAAAGTGC	4542
rs552758347	in-del	-/TTC			intron-variant	MYO1F	GRCh38.p7	19:8533333	GTGCCCAGCCTCAGA[-/TTC]TTCTTCTTCTTCTTC	4542
rs552775103	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8523990	CAGGCATGATGGCGT[A/G]TGCCTGTAGTCCCAG	4542
rs552789469	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8523801	CTGGGACTATAGGCA[C/T]ACACCACCATGCCCA	4542
rs552889118	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8545212	CCCACCTCAGCCTTC[C/T]GGGTAGCTGGGATTA	4542
rs552959476	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8546484	CTCATCTCAGCCTTC[C/T]GAGTAGCTGGGACCG	4542
rs553040361	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8568645	AAGTGGATTTGGCCG[C/T]GCATGGTGGCTCACG	4542
rs553078426	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8541760	ACATCAGAACTAGTC[C/T]ATAGAAACACCATCC	4542
rs553112871	in-del	-/CCTCTGCCTCCCTGGCTCAAGCGATT	0.0178098	0.0926698	intron-variant	MYO1F	GRCh38.p7	19:8566595	CTTGGCTCACTGCAA[-/CCTCTGCCTCCCTGGCTCAAGCGATT]CTCCTGCCTCAGTTT	4542
rs553145890	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8571320	TGGGGCCACACCCTG[C/T]GTCCATGCACTGTGC	4542
rs553149658	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8564051	TCTGAGGTTAATGTC[A/G]GGATTTAAAGGAGGC	4542
rs553155373	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8557301	ACAACCAAACAAACA[A/G]CAAAAAAAGTTTTGA	4542
rs553184540	snp	A/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8570614	CCAAGTGATCTGCCC[A/G]CCTTGACCTCCCAAA	4542
rs553441362	snp	A/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8576242	GACCTCAAGTGATCT[A/G]CCTGTCTCAGCCTCC	4542
rs553462024	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8535903	AGCCAGGATGGTCTC[A/G]ATCTCCTGGCCTTGT	4542
rs553473811	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8553595	TCTCTGCTCTCAGCC[A/G]GGCATGGTGGCTCCT	4542
rs553647433	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8531127	CTGAGGCGGGAAGAT[C/T]GCCTGAGGTCGGGAG	4542
rs553651256	in-del	-/TT			intron-variant	MYO1F	GRCh38.p7	19:8574599	TCTCTCTCTCTCTCT[-/TT]CTTTCTTTCTTTCTT	4542
rs553666943	in-del	-/TT			intron-variant	MYO1F	GRCh38.p7	19:8522039	TTTTTTTTTTTTTTT[-/TT]GAGACGGAGTCTCGC	4542
rs553678855	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	MYO1F	GRCh38.p7	19:8520445	ACTACAGGCGCCCGC[A/C]ACCACGCCCGGCTAC	4542
rs553682754	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8524970	TCGGAGGCCGAGACG[A/G]GCGGGTCACCTGAGG	4542
rs553787298	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578291	TTACAGGTGCCCACC[A/G]CCACACCTGGCTAAT	4542
rs553808147	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8537527	GCTCACTGCAACCTC[C/T]ACCACCTGGATCCAA	4542
rs553824848	snp	A/G	0.00517822	0.0506191	intron-variant	MYO1F	GRCh38.p7	19:8522196	CCCGGCTAATTTTTT[A/G]TATTTTTAGTAGAGA	4542
rs553842062	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	MYO1F	GRCh38.p7	19:8521107	CTTAGTAAGTTAACT[C/T]GTGCTTTCACCTGGC	4542
rs553867640	snp	A/G	0.000399281	0.0141238	synonymous-codon, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526484	CCCATCGCCCACGCT[A/G]ACCGTGAGGGTCCGA	4542
rs553958478	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8547967	CCCCTAGTTGCTAAG[A/G]GATCCTCATGGTCCT	4542
rs554011864	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8542361	CTGCAGCCTGGCGGG[G/T]GGGTCCCTGGGAGTC	4542
rs554019965	snp	C/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8548457	CAGCCCTCTTTAGCT[C/G]TGCCCTTCCTGGCTC	4542
rs554053404	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8522955	CCAGTGTGGTAAGGA[C/T]TGGGCCAGACGGAGG	4542
rs554086558	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8532075	GTGAGCGGAGATTGC[A/G]CCACTGCACTCCAGC	4542
rs554156014	snp	C/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8556180	ATTACAGGTGCCCAC[C/G]ACCATGCCCGGCTAA	4542
rs554200017	snp	C/G	0.00199481	0.0315187	intron-variant	MYO1F	GRCh38.p7	19:8572057	GTCTTTCTGGAGCTG[C/G]GCTCTTTGTCTCGTC	4542
rs554224458	snp	C/T	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8524371	GCAGTGCGCTGAGAC[C/T]GCACCATTGCACCCC	4542
rs554236160	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8565432	CTGTAATCCCAGCTA[C/T]TCGGGAGGCTGAGGC	4542
rs554268837	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8560670	GCCTTGACCTCCTGG[G/T]CTCAAGTGATCCTCC	4542
rs554329738	snp	G/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8555301	TTTGAATCCGGGAGG[G/T]GGAGGTTGCAGTGAG	4542
rs554392050	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	MYO1F	GRCh38.p7	19:8520324	TTTGAGATGGAGTCT[C/T]GCTCTGTTGCCCAGG	4542
rs554499098	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8549687	CCGGGTAATTTTTAG[C/T]AGAGAGGGGGTTTCA	4542
rs554513240	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8531245	CCAGCTACTCAGGAG[A/G]CTGAGGCAGGAGAAT	4542
rs554603738	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8559432	GGGCATTAAATAAGC[C/T]CAGCCTTTGGCATAA	4542
rs554610948	snp	C/G	0.000802729	0.020018	intron-variant	MYO1F	GRCh38.p7	19:8542303	GCTTGCATCAGAGGC[C/G]GGGGGGCGGTGAAAG	4542
rs554639650	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8525820	CAGTTCCAGGGTTGC[A/C]GCTCTGGCCGCACCC	4542
rs554701128	snp	C/G/T	0.000126095	0.00793926	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526423	CCTCGCTGGCCCCGC[C/G/T]CCCTCTGCCCTAGTT	4542
rs554727595	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8554316	TCAATAAAATACATC[A/G]TGAGTCAGATGGTGA	4542
rs554749803	snp	C/T	0.00199481	0.0315187	intron-variant	MYO1F	GRCh38.p7	19:8552896	TAGCATGGCTGCAGC[C/T]GGGGGAGCATTTAAG	4542
rs554784680	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8547929	ACAGAGAGGTGGGAA[C/T]GCGGTGGGGAGGGCT	4542
rs554883997	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8560301	CATCCTGGCTAACAT[A/G]GTGAAACCCCATCTC	4542
rs554887163	snp	A/G	9.96463e-05	0.00705785	intron-variant	MYO1F	GRCh38.p7	19:8554753	GTAGGTCTGAGGGAT[A/G]GTTAAGGGTCGTGTG	4542
rs554917567	snp	A/G	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8537422	ATAGGTACCTTGGGT[A/G]TTTGTTTTTTTTGTT	4542
rs554950420	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8549015	AATGCCAGTGGCGCA[A/G]TCTCGGCTCACTGAA	4542
rs554956277	snp	A/G	0.00597247	0.0543191	intron-variant	MYO1F	GRCh38.p7	19:8542839	CGATCTCCTGACCTT[A/G]TGATCCGCCCGCCTC	4542
rs555001565	snp	G/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8571947	CCAGGATGGTCTCGA[G/T]CTCCTGACTTCGTGA	4542
rs555040254	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578184	AGCTCTGTCACCCAG[A/G]CTAGAATGCAGTGGT	4542
rs555143003	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8567022	TCTTATCCTTTCAAC[A/G]CACGCTGGCTGAGGT	4542
rs555201186	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8538172	GGTTTCACCATGTTG[A/G]CTGGGCTGGTCTTCA	4542
rs555266935	snp	C/T	0.00517822	0.0506191	intron-variant	MYO1F	GRCh38.p7	19:8522179	AGGCGCCCGCCACCA[C/T]GCCCGGCTAATTTTT	4542
rs555335257	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8561064	TTTTTAAATATTTCA[G/T]AGAGACATGGTCTTG	4542
rs555385267	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8543354	GTAGCCTTCGGTAGG[A/G]GTCTGTAGGAGGCTT	4542
rs555627525	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8556380	AGTGCAGTGGCTCAT[C/G]CCCGTAATCCCAGCA	4542
rs555676450	snp	C/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8552547	GCTGGGATTTCAGAT[C/G]TGAGCCCCCACACCC	4542
rs555693888	snp	C/T	3.61696e-05	0.00425247	missense	MYO1F	GRCh38.p7	19:8522790	TCCAGGGGCAGGGGG[C/T]CCCCTCTGGCAGAGG	4542
rs555715911	snp	A/C/G	3.34729e-05	0.00409091	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8527409	CACCTGGCCCTTCTC[A/C/G]GGTCCCTTCTTCACT	4542
rs555753107	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8561649	TTCCTTCTTTCCTTC[C/T]ATTTTTTCTTTCCTT	4542
rs555754564	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8554248	AAGCATGAGCCACTA[C/T]ACCTGGCCTGAGGTG	4542
rs555778393	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8540383	TTTCTTTGTCACAAA[A/G]AGGGAACAACACGGA	4542
rs555817475	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578378	TCCTGACCTCAGGTG[A/G]TCCTCCCAACTCGGC	4542
rs555949929	snp	G/T			utr-variant-3-prime	MYO1F	GRCh38.p7	19:8521121	TCGTGCTTTCACCTG[G/T]CAAAGGTTTATTGCC	4542
rs555958026	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8555160	GCACTCCAGCCTGGG[C/T]AACAAGAGCCACTCA	4542
rs556000328	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8545098	ACGTCTTAAATTTAA[C/T]TTTTTTTGAGACAGG	4542
rs556004439	snp	A/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8550882	GGGCTTTGTTTTTTA[A/T]TATATTTTTTATTTT	4542
rs556010111	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8562586	TGTTGCCCAGGCTGG[A/G]GTGCAGTGGTGTAAT	4542
rs556019447	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8534342	TTTCAGAGTCTCACT[C/T]TGTCCCCCAGGCTGG	4542
rs556033128	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8543054	GATTACAGGTGCCCA[C/T]GACCACGCCCGGCTG	4542
rs556046520	snp	A/G	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8564186	AGGAGTTCGAGACCA[A/G]CCTGGCCAACATGGT	4542
rs556054718	snp	A/C/T	3.3764e-05	0.00410866	missense, synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8540017	TCGGGGAAGAGCATC[A/C/T]GGAGGAAGGCCCTGG	4542
rs556151815	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8566368	GAGATGGGCTTTCAC[C/T]GTGTTAGCCAGGATG	4542
rs556186566	snp	C/G	0.00597247	0.0543191	intron-variant	MYO1F	GRCh38.p7	19:8572611	TCCTAAATTCCTTTT[C/G]ACTCCCAGCCTTTCC	4542
rs556241579	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8533777	GCCATGGAGTTTGTG[A/G]AACTTTGTTTCAGCT	4542
rs556335167	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8544155	GGGGGTGGATTGAGG[C/T]GGGGGACAGTGGAAT	4542
rs556403792	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8537649	ATGTTGGTCAGGCTG[C/G]TCATGAACTCCTGAC	4542
rs556421866	snp	A/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8558633	GTCTCTATTCAACAC[A/G]TCTCTGCAAAGGAGT	4542
rs556429876	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8544012	TGGTGGTGGCGGTGG[C/T]GGTGGCGGTGGCGGT	4542
rs556463746	snp	C/G	0.00398564	0.0444627	intron-variant	MYO1F	GRCh38.p7	19:8544658	GGATGGAAGGGATAG[C/G]GGGGCAAGGGTGTGT	4542
rs556474325	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8574912	AGGCGCGCACCACCA[C/T]GACTGGCTAATTTTT	4542
rs556482436	snp	A/G	1.66882e-05	0.00288857	intron-variant	MYO1F	GRCh38.p7	19:8527322	GACTGTGCGGCAGGT[A/G]AGGACCTGGCTTCAC	4542
rs556534755	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8532129	TCCCCCGACCCCTGA[A/C]AAAAGAAAAGAATGA	4542
rs556547552	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8543834	GTGGTGGTGGTGGTG[C/G]TGGTGGTGGTGGTGG	4542
rs556590000	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8561028	AGGTGTGAGCCACTG[C/T]GCCTGGCCACGCCTG	4542
rs556624001	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8560720	AGCTGAGACTACAGG[C/T]ACATGCCACCACGCC	4542
rs556648595	snp	A/T	0.00318978	0.0398085	intron-variant	MYO1F	GRCh38.p7	19:8555367	GGGCGACAGAGCAAG[A/T]CTCCGTCTCAAAAAA	4542
rs556679736	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8567811	CGGGGTTGCTGCTGA[G/T]GTCAGATGAGGATGG	4542
rs556773318	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8550428	CTGCATGGGCCTCCT[A/G]TTATCCCCATCTTGC	4542
rs556792875	snp	C/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8557146	AGAAAAATTAGACGA[C/G]TGGTGGCATGTGTCT	4542
rs556797150	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8524339	GAGAATCTCTTGAAC[C/T]CAGAAGGTGGAAAGT	4542
rs556810756	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8528132	GAGGCTGAGACAGGA[A/G]AATCGCTTGAACCCA	4542
rs556868032	snp	A/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8562542	AAAATTTATTTACTT[A/T]TTTATTTTTTTGAGG	4542
rs556983933	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8568500	TGCTCAAGTGAATAT[C/T]GTGTGGGGAGGATAG	4542
rs557130177	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8569951	AGTCTTGTTCTGTTG[C/T]CCAGGTTGGAAGGCA	4542
rs557131769	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8576890	CGGATTTCCAAATAT[A/G]ACATCTGTGGGAACC	4542
rs557149806	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8562139	TCCAGGGTTCACGCC[A/G]TTCTCCTGCCCGGCT	4542
rs557166880	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8576201	ACGAGGTTTCACCAC[A/G]TTGGCCAGGCTGGTC	4542
rs557191492	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8570509	GTAGCTGGGATTACA[A/G]GTGCACGCCACCACA	4542
rs557201019	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8537832	CCTCCTGTGCTCAAG[C/T]GATCAACTGCCTTAG	4542
rs557295414	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8545043	TTGGCCTCCCAAAGT[A/G]CTGGGATTACAGGCA	4542
rs557332355	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8544595	TTTGGGGGTGGGGAG[C/G]GCACCAGGGGCTTCA	4542
rs557419872	in-del	-/T	0.0023933	0.0345097	intron-variant	MYO1F	GRCh38.p7	19:8549504	CATACATTAAAAAAG[-/T]TTTTATTTTATTTAT	4542
rs557457704	snp	A/C	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8539425	ATCTCAAAAAAAAAA[A/C]CAAACCAACAAAAAA	4542
rs557462971	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8548833	GACCTCGTGATCCGC[C/T]CGCCTCGGCCTCCCA	4542
rs557487405	in-del	-/TC			intron-variant	MYO1F	GRCh38.p7	19:8574648	TTTCTTTCTTTCCTT[-/TC]TCTTTCTCTTTCTTC	4542
rs557499869	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8549992	TCTGTAGAGATGGGG[G/T]TCTTGCTATGTTGCC	4542
rs557557399	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8567774	GCTGTCCTTCCCCAG[A/G]CTGGTCTGTATCAGA	4542
rs557583506	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8562121	CTCACTGCAAGCCTC[A/G]CCTCCAGGGTTCACG	4542
rs557590823	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8563391	CAACCTCTGCTTCCC[A/G]GATTCAAGCGATTCT	4542
rs557633606	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8523858	AGGCGCGGTGGCTCA[C/T]GCCTGTAATCCTAGC	4542
rs557717296	snp	A/C	0.0368353	0.130617	intron-variant	MYO1F	GRCh38.p7	19:8555886	TCTGGGTTCTGTCCC[A/C]CCTCCCCCGCCCCAC	4542
rs557720157	snp	A/G	1.67427e-05	0.00289328	missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536323	CCATGTTGACCGCCC[A/G]AAGCAGGTGCTGGAC	4542
rs557774287	in-del	-/TA	0.00438332	0.0466095	intron-variant	MYO1F	GRCh38.p7	19:8528856	TGTGTATCTGAACTC[-/TA]TGAGTTTGTACAGGA	4542
rs557781069	snp	A/G	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8528449	AGGAGAATTGCTTGA[A/G]CCTGGGAGGCAGAGG	4542
rs557828877	in-del	-/G	0.00358779	0.0422022	intron-variant	MYO1F	GRCh38.p7	19:8532889	TGAGATCCTGTCTCA[-/G]AAAAAAAAAAAAATA	4542
rs557834627	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8543978	GTGGTGGTGCTGGTG[C/G]TGGTGCTGGTGGTGG	4542
rs557884887	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8528088	TTAGCTGGGCGAGGT[C/G]GTGGGCACCTGTAGT	4542
rs557897916	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8543846	GTGGTGGTGGTGGTG[C/G]TGGTGGTGGTGCTGG	4542
rs557986656	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8523506	GTATGCTCCACTATG[C/T]CCAGTTGATTTTTAT	4542
rs558008773	snp	C/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8551420	GCAGTAGTGTGATCT[C/T]GGCTCACTGCAACTT	4542
rs558064312	snp	C/T	0.00358779	0.0422022	intron-variant	MYO1F	GRCh38.p7	19:8523185	TACAGGCACCTGCCA[C/T]CACGCCTGGATAATT	4542
rs558069088	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8545971	CTCCCTCGCTTCTCC[A/G]CTCTATGAAGCCTCC	4542
rs558108333	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8551006	CTGCCTCCGCCTCCC[A/G]AGTAGCTGGGATTAC	4542
rs558140748	snp	C/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8576831	CACAGACCTTGAGAA[C/T]GTTGCAACTGAAAGA	4542
rs558339515	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8549403	AGCCTCCTGAGTAGC[C/T]GGGATTACAGGCACC	4542
rs558347430	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8540408	CACGGATAAATTGTA[C/G]ATTTTAAAATGGTTA	4542
rs558393129	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8569306	TGACTCAACCTGCTG[A/G]AGCTCTTGTGAAAGG	4542
rs558433823	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8575436	GTGCAGTTCACAACA[A/G]GGTTTGCGATCCTGT	4542
rs558479901	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8535810	TCAGCCTCCTGAGTA[A/G]CTGGGACCACAGGTG	4542
rs558503644	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8542173	ATAGGGGATGGGGGG[C/T]GGGCTTCCTGGAGAG	4542
rs558515732	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8535287	TTGTTGATGTTCTTA[C/T]AGGATTTTACCACTA	4542
rs558531413	snp	G/T	0.00199481	0.0315187	intron-variant	MYO1F	GRCh38.p7	19:8523723	GCAGCAGTGAGATCA[G/T]AGCTCACTGCAGACT	4542
rs558540295	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8541813	GAGTTTGTGGCGAGA[C/T]GGCAGTTCTGGGTAA	4542
rs558604420	snp	A/G	0.0123036	0.0774623	intron-variant	MYO1F	GRCh38.p7	19:8576866	TGAAGAGCAACTTCC[A/G]CATCTAGACGGATTT	4542
rs558617548	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8547180	ATGGTGTGTGCCTGC[A/G]GTCCCAGCTACTTGA	4542
rs558717291	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8564532	AGGAACTGCCAGGGA[A/G]GTCAGAGGCAAAACC	4542
rs558745656	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8571377	CCATCCCTCAGGGGA[G/T]CAGGGGGACTGGACT	4542
rs558746294	in-del	-/T	0.00716266	0.059414	intron-variant	MYO1F	GRCh38.p7	19:8561602	CCTCCCTCTCTTCTC[-/T]TTTTTTCTTTCTCTC	4542
rs558780775	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8553679	AAAGTTAGAGACCAG[C/T]CTGGCCAACATGGTG	4542
rs558844738	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8525126	AATCGCTTGAATCCA[A/G]GAGGTGAAGGTTGCA	4542
rs558917294	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8564549	TCAGAGGCAAAACCC[A/G]GACCAGGCAGGGGAG	4542
rs559011220	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8570914	AGTTTCCTCATTCGG[A/C]AAATGGGAACATCGA	4542
rs559030527	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8577246	GTCATTTTTAGGACA[C/T]CTCCACCTGGCTGGT	4542
rs559043787	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8530761	AGAAGAAAAAGGGGC[C/T]GGGCGCAGTGGCTCA	4542
rs559085544	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8562185	TTTTTGTATTTTTAG[C/T]GGAGACGAGGTTTCA	4542
rs559095239	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8577625	CCCAACTCCTTGGGG[A/G]CAGGGCTGCTGCAGG	4542
rs559098832	snp	A/G/T	0.000165666	0.00909985	intron-variant	MYO1F	GRCh38.p7	19:8545753	TGGGGTGGAAAAGGG[A/G/T]GTGGATGTGGGGGCC	4542
rs559143941	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8556685	CTGAGGACGAGAGTT[C/T]GAGACCAGTCTGATC	4542
rs559146134	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8551145	CAACCTCCACCTCCC[A/G]GGTTTAAGCGATTCT	4542
rs559263239	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8546030	TGTCCACAGCATAAC[A/G]TGCTCATTAACACAC	4542
rs559272215	snp	A/G/T	1.7182e-05	0.00293099	intron-variant	MYO1F	GRCh38.p7	19:8521640	TGAGGTGCCCCTAGC[A/G/T]GGCCCTGGAGAAAGC	4542
rs559335346	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8561864	TGGGACTATAGGCGC[A/G]CACCACCACACCCGG	4542
rs559386575	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8562885	CATGCCGGTGGTGGC[A/G]TTAAAAATGACCTGT	4542
rs559482300	in-del	-/AAAGAAAGAAAG	0.0652144	0.168387	intron-variant	MYO1F	GRCh38.p7	19:8556483	CCCGTCTCTATAAAA[-/AAAGAAAGAAAG]AAAGAAAGAAAGAGA	4542
rs559555784	snp	C/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8563449	ATTATAGGCGTGCAC[C/T]ACCACGCCCAGCTAA	4542
rs559578446	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8575084	TTTCTTTTTCTTTTT[C/T]TTTTTTTTTTGAGAC	4542
rs559690173	snp	A/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8558201	CAGAGTCTTGTTCTG[A/T]CACCCAGGCTGGAGT	4542
rs559757515	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8552406	TGGGACTACAGGCAC[C/G]CGCCACCATGCCCAG	4542
rs559879332	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8523410	TGCAGTGGTACAATC[A/G]TAGCTCACTGCAACT	4542
rs559911784	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8529803	GCTATACTTGAGTGT[A/C]TACCTGTGGGCAGGT	4542
rs559936551	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8523925	GGAGTTTGAGACAAG[C/T]CTGGCCAACATAGTG	4542
rs559975389	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8549043	GAAACCTCTGCCTCC[A/G]GGATTCAAGAGATTC	4542
rs560040683	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8546552	TTTTGTAGAGATGAG[A/G]TCTCACTATGTTGTC	4542
rs560055375	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8531006	CTGAGATCGCGCCAT[G/T]GCACTCCAGCCTGGA	4542
rs560086044	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8543699	GTGGTGGTGGTGGTG[C/G]TGGTGGTGCTGGTGG	4542
rs560090185	snp	A/G	1.7174e-05	0.00293031	intron-variant, missense, utr-variant-3-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536606	CTTGACTCTGGTGGG[A/G]AGGGTAGGCTGAGTC	4542
rs560118407	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8552998	GCAGGAAGTGAGTCT[C/G]CCCTTCAGGAGTAGG	4542
rs560131117	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8571199	GTGGTTGCCGGGAGG[A/G]GAGCTAAGCCTCCGT	4542
rs560166734	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8541627	AGAGACAAGGTTTTG[C/T]CATGTTGCCCAGGCT	4542
rs560215723	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8546733	GCCCAGGCTGGAGTG[C/T]AATGGCACAATCTCG	4542
rs560231342	snp	C/T	0.0023933	0.0345097	intron-variant	MYO1F	GRCh38.p7	19:8521874	TGCCCAGGCTTGTCT[C/T]AAACTCCTGACCTCA	4542
rs560235538	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578784	AGGAGGTGGCCGAGG[A/C]AGGACCCGACCCTGG	4542
rs560327516	snp	A/G	5.10895e-05	0.00505392	intron-variant	MYO1F	GRCh38.p7	19:8542020	TGCTGAGGACAGTGA[A/G]GGACTGAGAAACCTG	4542
rs560381517	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8560609	AGACAGGGTCTCACT[C/T]TGTCTCCCAGGCTGG	4542
rs560400072	snp	C/T	0.0162398	0.0886349	intron-variant	MYO1F	GRCh38.p7	19:8571575	GCCCGCCACCGCGCC[C/T]GGCTAATTTTTTTTT	4542
rs560446032	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8542437	GCAGGGGGCCTGTGT[C/T]AGGAGGGTAACAGCC	4542
rs560465879	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8564267	GCGCCTGTAATCCCA[C/G]CTACTTGGGAGGCTG	4542
rs560479730	snp	C/G			intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526376	CTCTCTGTAGACACT[C/G]CCCTTCCTGGCCTTC	4542
rs560487822	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8560325	CCATCTCTACTAAAA[A/G]TACAAAAAAAGTAGC	4542
rs560499772	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8559772	CTGACCAACATGGTG[A/G]AACTCCATCTCTACT	4542
rs560519909	snp	G/T			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578572	ACAGCCTCCAGTTTG[G/T]CTACTTCCTGGATGA	4542
rs560585816	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8554418	ACCTCCCTGGGGGTG[A/G]TGATGTTTCAGCAGG	4542
rs560599012	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8572238	CTGATTCATTGTTAC[A/G]TTCACTCTTTGCATC	4542
rs560717984	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8536148	CTATCAGTCTTTCTC[C/T]CAATCTCTGTCTCCC	4542
rs560750674	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8548741	AAGTAGCTGGAACTA[A/C]AAGGGCCTGCCACCA	4542
rs560753613	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8549108	GGCATGCGCCACCAC[A/G]CCCGGCTAATTCTTG	4542
rs560848649	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8552337	AATGTCGGCTCACTG[C/T]AACGTCCACCTCCTG	4542
rs560864572	snp	C/T	0.00199481	0.0315187	intron-variant	MYO1F	GRCh38.p7	19:8545244	AGGCGCCTGCCACCA[C/T]GCCTGGCTAATTTTT	4542
rs560918894	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8524738	CCAGGAGTGGCTTTG[C/T]AGGGGCAAGTTTCCC	4542
rs561005433	snp	C/T	1.65146e-05	0.0028735	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8553196	GAAGGCCTCGAGCAG[C/T]GGGTTGGACTGCAGG	4542
rs561105033	snp	G/T	1.67464e-05	0.0028936	intron-variant	MYO1F	GRCh38.p7	19:8541881	GGGGTTGTAGCCGGA[G/T]GTCCCCATGCCTGGG	4542
rs561111788	snp	C/G	0.00199481	0.0315187	intron-variant	MYO1F	GRCh38.p7	19:8576590	CACGACAGTCTCCCC[C/G]TTGCTATCATCGACA	4542
rs561120534	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8559132	CGACCTTCCTGCCTC[A/G]ATCTTCCAAACTGCT	4542
rs561129153	snp	C/T	0.000248457	0.011143	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8548089	GCAGCTTCTCATTGA[C/T]GAAGTTGATGCAAAA	4542
rs561157294	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8564210	ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA	4542
rs561167848	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8547626	AAAAAAAAAATCCCT[A/G]ACTTACTTCCTCAGT	4542
rs561173234	snp	C/T	0.000369702	0.013591	intron-variant	MYO1F	GRCh38.p7	19:8577265	CACCTGGCTGGTGTC[C/T]CTCCTCTTTCTTCTT	4542
rs561181492	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8544762	AATCCCTTGGTAGGG[G/T]GACCTGCCTTATGTA	4542
rs561210840	snp	G/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8563702	TTTTTAGTAGAGATG[G/T]GCTTTCACTATGTTG	4542
rs561327055	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8546211	CTGGGATTACAGGTA[C/T]GTGCCACCACGCCGG	4542
rs561388324	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8523187	CAGGCACCTGCCACC[A/G]CGCCTGGATAATTTT	4542
rs561389886	snp	C/T	0.00398564	0.0444627	intron-variant	MYO1F	GRCh38.p7	19:8559677	TAACACGACCGGGCG[C/T]GGTGGCTCACACCTG	4542
rs561392255	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8571699	GCCTCCCGAGTTCAC[A/G]CCATTCTTCTGCCTC	4542
rs561414901	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8572620	CCTTTTGACTCCCAG[C/T]CTTTCCTGTCCATCC	4542
rs561513224	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8561993	GTGCTGGGATTACAG[G/T]CATGAGCCACTGCGT	4542
rs561584687	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8566400	TCTCGAGCTCCTGAT[C/G]TCATGATCCACCCGC	4542
rs561634752	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8541578	GAATTACAGGTGCGC[A/G]CCACCACGCCTAGGT	4542
rs561636459	snp	A/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8531388	GGGTCTCGCTCCGTC[A/G]CCCAGACTGGAGTGT	4542
rs561665230	in-del	-/CAAAGCACTG	0.0023933	0.0345097	intron-variant	MYO1F	GRCh38.p7	19:8562260	CCCGCCTTGGCCTCA[-/CAAAGCACTG]GGATTATAGGCATGA	4542
rs561693690	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8537705	TCCCAAGGTGTTGGG[A/G]TTACAGGCATGAGCC	4542
rs561728134	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8553745	GACATGGTGGTGGGC[A/G]CCTGTAATCCCGGCC	4542
rs561728709	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8543076	GCCCGGCTGATTTTT[A/G]TATTTTTAGTAGAGA	4542
rs561758236	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8532253	CTGCACAGCCATCCG[C/T]AGCAGGCCCAGAAAG	4542
rs561758297	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8526118	TGGAGCATGAGGTAA[C/T]GAGTTCAAGACCAGC	4542
rs561767346	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578430	AGGCATAAGCCACCA[C/T]GCCTGGCCCAACCTC	4542
rs561818983	snp	C/G	2.60787e-05	0.00361091	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8526794	GGGGCCGTACGTGTC[C/G]CTGAAGGTGAGGGGC	4542
rs561918981	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8560791	TCGCCCAGGCTGGAG[C/T]GCAGTGGCACGATCT	4542
rs562031796	snp	A/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8522238	TGTGTTAGCCAGGAT[A/G]GTCTCGATCTCCTGA	4542
rs562037051	snp	A/G	0.00517822	0.0506191	intron-variant	MYO1F	GRCh38.p7	19:8528182	AGCCGAGATCCTGCC[A/G]CTGCACTCCAGCCTG	4542
rs562045489	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8549911	GTTCAAATGATCCCC[A/C]AACCTCAGCCCTCTG	4542
rs562075817	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8527699	CTCACTGCAACCTCC[C/T]CCTCCTGGGCTTGAG	4542
rs562108071	snp	A/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8539664	TTTTACCACAAATTT[A/T]AAAAATGGTAAATGA	4542
rs562192928	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8577408	CTTGGGCATGGCCCT[A/G]CTTCTGCCCGTTCAC	4542
rs562205481	snp	A/C	0.00636936	0.0560724	intron-variant	MYO1F	GRCh38.p7	19:8544718	AGAAGTGGGTGGGGA[A/C]CCCTCAAGAGATTCA	4542
rs562276039	snp	C/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8533879	GGATGGCCCAAACCA[C/T]GTTCATAAGAAAATC	4542
rs562277075	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8533272	GGGCTCAAGGAATCT[A/G]CCAGCCTTGACCTCC	4542
rs562311599	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8539143	AATTAGGCCGAGCGC[C/G]GTGGCTCACACCTGT	4542
rs562315096	snp	A/T	0.00318978	0.0398085	intron-variant	MYO1F	GRCh38.p7	19:8573299	CTGGGTGACAGAGCG[A/T]GACTCTGTCTCAAAA	4542
rs562341714	snp	C/G	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8568003	TCTGACGACTTGGTT[C/G]CTCTTCCTGCCCTTC	4542
rs562375978	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8574281	CAGCAATGACCACTC[A/G]CAGCAACTCCTCCCC	4542
rs562416132	snp	A/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8571621	TTATTGTTTTGAGAC[A/G]GAGTCTTGCTCTCTC	4542
rs562451544	snp	A/G	4.28146e-05	0.00462661	intron-variant	MYO1F	GRCh38.p7	19:8536651	AGTCACCAGTCCTGG[A/G]GGTGGGTGGGAGGTG	4542
rs562611528	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8543876	GTGGTGCTGGTGGTG[C/G]TGGTGGTGGTGGTGG	4542
rs562618216	snp	A/G	2.83724e-05	0.00376635	intron-variant	MYO1F	GRCh38.p7	19:8537085	AAGACGGGTGGGTGG[A/G]GGGCACAGAGATGGG	4542
rs562652794	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8572624	TTGACTCCCAGCCTT[C/T]CCTGTCCATCCTCAT	4542
rs562679539	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8531374	AAAAGAAAAAGACAG[C/G]GTCTCGCTCCGTCGC	4542
rs562727255	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8538483	GATGGGCTTTCACCA[C/T]GTTGGCCAGGCTGGT	4542
rs562743218	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8572017	CGTAAGCCACCGCGC[C/G]TGGCCTTTATACGTG	4542
rs562765685	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578900	CCCCTAGTGGCCACA[G/T]CTGGGAAGGAGCCCG	4542
rs562768863	snp	G/T	0.00119737	0.0244387	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526690	AGGGGCGGGGCCGCG[G/T]CCGGGGCCGAAGCGC	4542
rs562795461	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8521971	TTATCTCTGTTCTCC[C/T]GTGGGGAGGGTGTGC	4542
rs562799875	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8543488	GGGTTATGACTCACA[C/T]TGGGGCTTATCTGAA	4542
rs562838368	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8526067	GGCGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA	4542
rs562863964	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8554926	CGGTGGCTCATGCCT[A/G]TAATCCCAGCACTTT	4542
rs562887958	snp	C/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8532571	AAAGGGACAATATTG[C/T]CAATTAGTGAAGATG	4542
rs562941695	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8573364	GACCACCATCACCAA[C/G]CAAAGGCAACCAGTG	4542
rs562943526	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8550911	TTTGAGACAGAGTCT[C/T]CCTCTGTTGCCCAGG	4542
rs562955079	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8549169	CTGGCCAGGGCTGAT[C/T]TTGAACTCCTGACCT	4542
rs562975523	snp	A/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8530714	TTTTTTAAGAGGCGG[A/G]GTCTTTCTAGTGACA	4542
rs562980220	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8552748	TCAAACCCTGAATCC[A/C]TATCTGTTTACCTAT	4542
rs563011851	snp	A/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8566521	TTAATTTAATTAATT[A/T]ATTTATTTTTGAAAC	4542
rs563135856	snp	C/T	0.000364534	0.0134957	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550641	GATCCCCGCCACGAG[C/T]TGCAGGACCAGCTGC	4542
rs563162498	snp	A/G	0.0267878	0.112589	intron-variant	MYO1F	GRCh38.p7	19:8555941	AGGAGAGGCTGGCAG[A/G]GTCCAAGCCAGGCCC	4542
rs563166463	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8569603	AGAACCTGCCCTTGG[A/G]GGGCTCGGTGTTCCC	4542
rs563278807	in-del	-/TTTTTTTTTTTT	0.384209	0.210922	intron-variant	MYO1F	GRCh38.p7	19:8546057	ACACTATTTTGACTC[-/TTTTTTTTTTTT]TTTTTTTTTTTTTGA	4542
rs563516715	snp	C/T	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8540119	GCCTCAATGCCGCAA[C/T]GCAAAATATGGTTCT	4542
rs563551822	snp	A/G	4.968e-05	0.00498373	synonymous-codon, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8545677	GATGAGGTCACAGAC[A/G]ACCTTGTTGTTGAAG	4542
rs563656019	snp	C/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8533958	GGGAGGCTGAGGTGG[C/G]CAGATCACTTGAGGT	4542
rs563722140	snp	C/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8539855	TGGTAGACAGACAGA[C/T]GTTGGAATGAGAGAA	4542
rs563773311	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8568789	AGCCCGGCGTGGTGG[C/T]GGGTGTCTGTAGTCT	4542
rs563801319	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8567068	GTCCAATTTTTTTTT[C/T]TTTTTTTTTTTGAGA	4542
rs563897244	snp	C/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8559169	ACAGGCATGAGCCAC[C/T]GCTCCCAGCCCAGGA	4542
rs563907004	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8546415	CCCAGGCTGGAACTC[A/G]GCGATGCGATCCTAG	4542
rs563938853	snp	C/T	0.00398564	0.0444627	intron-variant	MYO1F	GRCh38.p7	19:8562250	TCGTTACCCGCCCGC[C/T]TTGGCCTCACAAAGC	4542
rs564086182	snp	A/G	0.00186496	0.0304796	intron-variant	MYO1F	GRCh38.p7	19:8539915	CTCAGCCCTCTGCAG[A/G]CCCAGCTCCCCGTTG	4542
rs564090560	in-del	-/G	0.0107289	0.0724523	intron-variant	MYO1F	GRCh38.p7	19:8542303	CTTGCATCAGAGGCC[-/G]GGGGGGCGGTGAAAG	4542
rs564133769	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8543684	GTGGTGCTGGTGGTG[C/G]TGGTGGTGGTGGTGG	4542
rs564152556	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8572714	TTATTTATTTGTTTA[A/G]AAACAGAGTCTGTCT	4542
rs564160553	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8522258	CGATCTCCTGACCTC[A/G]TGATCTGCCCGCCTT	4542
rs564186106	snp	A/C			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8577994	TGATTGCGCCACTGC[A/C]CTCCAGCCTGGGCGA	4542
rs564272377	snp	C/T	0.00517822	0.0506191	intron-variant	MYO1F	GRCh38.p7	19:8557955	GGTCCCTTTGAGCTC[C/T]TCCAGGCCACCATGT	4542
rs564337067	snp	A/C	1.65685e-05	0.00287819	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550569	ACACTCACGGTCCAC[A/C]CTCTCCACTCGGGCG	4542
rs564338507	in-del	-/AA	0.00199481	0.0315187	intron-variant	MYO1F	GRCh38.p7	19:8526031	TTGCGGCCTTTGTTT[-/AA]AAGTCTGTCTCTCTG	4542
rs564358880	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8549960	TGCACACCACTACAC[C/T]CAACTAATTTGAAAT	4542
rs564437591	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8523250	ATGTTAGCCAGGATG[A/G]TCTCGATCTCCTGAC	4542
rs564459063	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8539199	GCAGGCGGATCACCT[A/G]AGGTCGGGAGTTCGA	4542
rs564473235	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8523107	CGCGATCTCGGCTCA[C/T]TGCAAGCTCCGCCTC	4542
rs564495157	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8544771	GTAGGGGGACCTGCC[C/T]TATGTATTTATTTAT	4542
rs564519823	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8575998	GGATGCCCAATTTCT[C/G]ATCAGCTTTCCTTTT	4542
rs564562866	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8574914	GCGCGCACCACCACG[A/G]CTGGCTAATTTTTGT	4542
rs564564792	snp	A/G			utr-variant-3-prime	MYO1F	GRCh38.p7	19:8521145	TATTGCCTTAGTGAT[A/G]ACAGAATGAGCAAAG	4542
rs564620289	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8539811	TGCTGAACAGATGAC[A/G]TCACAGTCAGAGGCA	4542
rs564675415	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8528257	TAACAGATCAGGCGC[A/G]GTGGCACACGCCTGT	4542
rs564712749	snp	A/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8533913	ATAGGGGCCGGGCGC[A/G]GTGGCTCATGCATAT	4542
rs564725932	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8523177	GCTGGGACTACAGGC[A/G]CCTGCCACCACGCCT	4542
rs564738098	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8562237	TGATCTCCTGACCTC[A/G]TTACCCGCCCGCCTT	4542
rs564780806	snp	C/T	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8551585	TTAAACTCCTGACCT[C/T]AAGTGATCTACCTGC	4542
rs564812717	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8531703	TGCTTTTGCAAGAAA[C/T]GGTATGATGTCACGG	4542
rs564833295	in-del	-/A/AA	0.00914312	0.0669923	intron-variant	MYO1F	GRCh38.p7	19:8539414	GTGAAACTCCATCTC[-/A/AA]AAAAAAAAAACCAAA	4542
rs564863137	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8557327	TTTGAGACAGGGTCT[C/T]ACTCTGTCACCCAGG	4542
rs564888970	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8551189	CCCTAGTAGCTGGGA[C/T]TACAGGCGCATGGCA	4542
rs564926115	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8543888	GTGCTGGTGGTGGTG[C/G]TGGTGGTGCTGGTGG	4542
rs564964437	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8544030	TGGCGGTGGCGGTGG[C/T]GGTGGCGGTGCTGGT	4542
rs565042776	snp	C/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8563597	CACTGCAACCTTCGC[C/G]TCCCGGGTTCAAGCG	4542
rs565128167	snp	G/T	1.65405e-05	0.00287576	intron-variant	MYO1F	GRCh38.p7	19:8553123	AGCTGCTCCAAGCAG[G/T]TCTGCAGAGACTTAC	4542
rs565219362	in-del	-/AAAAAAAAAAAAA	0.383439	0.21141	intron-variant	MYO1F	GRCh38.p7	19:8556888	GTGAAACTCTGTCTC[-/AAAAAAAAAAAAA]AAAAAAAAAAGGAAG	4542
rs565262339	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8542582	CATGGGAGCTCCAGC[C/T]GTTTTTGTTTTTGTT	4542
rs565325231	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8544584	GGAGCTAGAGCTTTG[G/T]GGGTGGGGAGGGCAC	4542
rs565377094	snp	G/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8524541	AGTGAGCCAAGATCA[G/T]GCCACTGCACTCCAG	4542
rs565386915	snp	C/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8545019	TTGGCCTCAGGTGAT[C/T]CACCTGCCTTGGCCT	4542
rs565392554	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8547552	GAGGTTGCAGTGAGC[C/T]GAGATCATGCCACTG	4542
rs565502921	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8552498	TCTTGAACTCCAGAC[C/T]TCAAGTGATCCGCCT	4542
rs565651361	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8567741	AGTGCAGAGAGGACC[C/T]TGGGGAGGACCCACG	4542
rs565776466	snp	A/G	0.00398564	0.0444627	intron-variant	MYO1F	GRCh38.p7	19:8568878	GTGAGCCAAGATTAC[A/G]TCATTGCACTCCAGC	4542
rs565776556	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8562104	CAGTGGCACAATCTC[A/G]GCTCACTGCAAGCCT	4542
rs565881619	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8539363	AGGTTGTGGTGAGCC[A/G]AGATCACGCCATTGC	4542
rs566005254	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8569838	TGGAGGGATAGACAG[C/G]CCAGGCCATGTGGGG	4542
rs566042521	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8529172	CCAGGCCATATGAGA[C/T]TATCCATCCAGGTAA	4542
rs566168201	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8551350	AGCCACCGTGCCTGG[C/G]CTTTTTTTTTTTTTT	4542
rs566275232	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8545491	GAATGGATGAGGGGC[A/G]GAAGGGACATTTTGG	4542
rs566296087	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8575996	CGGGATGCCCAATTT[C/T]TCATCAGCTTTCCTT	4542
rs566316650	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8545167	ATCATAGCTCACTGC[A/C]CCCTTGACTTCCTGG	4542
rs566320889	snp	C/T	0.00636936	0.0560724	intron-variant	MYO1F	GRCh38.p7	19:8535740	GCTGGAGTGCAGTGG[C/T]GTGATCTCGGCTCAC	4542
rs566338124	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8540395	AAAAAGGGAACAACA[C/T]GGATAAATTGTACAT	4542
rs566348833	in-del	-/G	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8547945	GCGGTGGGGAGGGCT[-/G]GGGTGTCCCCTAGTT	4542
rs566420995	snp	A/T	0	0	utr-variant-3-prime, downstream-variant-500B	MYO1F	GRCh38.p7	19:8520796	TTTTTTTTTCTTTTT[A/T]AAATTTTTAGTAGAA	4542
rs566483228	snp	C/T	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8558750	CCCCCATCCCCAGGC[C/T]AGGAGCTCCTGGAGA	4542
rs566486660	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530121	GATATCTGGCTGTGG[A/G]CAGGTGCATCTGGGC	4542
rs566517555	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8547697	ATTTGTCTCTGAATC[C/T]TTGCCTCAGGCTCTG	4542
rs566548728	snp	A/G	0.00199481	0.0315187	intron-variant	MYO1F	GRCh38.p7	19:8563117	CTGTCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC	4542
rs566555142	snp	A/C	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8547105	GAGTTCAAGACCAAT[A/C]TGGGCAACAAAGTGA	4542
rs566578557	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8576721	GCCTCTGCTGCAGCC[A/G]TACCGCCCGTCACCG	4542
rs566587724	snp	A/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8542159	ATCTACAGTTCAGAA[A/T]AGGGGATGGGGGGCG	4542
rs566591035	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8569773	GAGAGGCCTTGGGTG[G/T]GTGGTGGACACCAGG	4542
rs566600644	snp	G/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8536194	CTCTCTCAGTCCCTC[G/T]CTATACCTTTCTCTC	4542
rs566709922	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8563737	GGCTGGTCTGGAACT[A/C]CTGACCTCAGGCGAT	4542
rs566729947	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8522235	CACTGTGTTAGCCAG[A/G]ATGGTCTCGATCTCC	4542
rs566903364	snp	A/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8571321	GGGGCCACACCCTGC[A/G]TCCATGCACTGTGCA	4542
rs567091174	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530022	AACAGATGGATCTAG[C/G]CTGGGGGATCTATGC	4542
rs567166187	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8571752	ACAGGCACCCGCCAC[A/C]ACGCCTGGGTAATTT	4542
rs567270372	snp	C/G	1.67967e-05	0.00289794	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8539997	TCTTGTCTCCATCCA[C/G]CTTCTCGGGGAAGAG	4542
rs567312069	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8546453	CAACCTTGACCTCCA[A/G]GGTTCAAGTGATCCT	4542
rs567357493	snp	C/T	0.000165593	0.00909775	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8552103	TTCTCCAGCAAGAAG[C/T]TGGAGATCTTGCCCC	4542
rs567382129	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8547007	TTGTTAAAAAAATCC[C/T]TGTCTCAGGACTGGG	4542
rs567423391	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8557847	AGGCCCAGGCCAGTC[C/T]CTGACTTCTCTGTGG	4542
rs567460235	snp	C/T	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8563070	GATCGCAGCTCACTG[C/T]AACCTCTGCCTCCCG	4542
rs567475494	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8576905	GACATCTGTGGGAAC[C/T]GGGGCCAAGAGAGGG	4542
rs567602943	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8571285	GGCCCTGGAGCCTTG[C/T]CCCCAGCTCAGTGGG	4542
rs567659574	in-del	-/T/TT	0.00623371	0.0554797	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526640	GGGCGCTGGCTGAGG[-/T/TT]TCCCCCGCCCCACCC	4542
rs567688212	snp	G/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8558476	TGACCCAGACGACAC[G/T]TTCTTTAGGCCCCAT	4542
rs567753091	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8543822	GTGCTGGTGGTGGTG[C/G]TGGTGGTGGTGGTGG	4542
rs567777789	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8541682	GATTTGTCCACTTCG[C/G]CCTCCCAAAGTGCTG	4542
rs567825680	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8564974	GACAGGATTTCACCA[C/T]GTTGGACACGCTCAT	4542
rs567826253	snp	A/G	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8542133	AGTGTCTACAGCGCT[A/G]GCTGGGGGGTATCTA	4542
rs567938104	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8573365	ACCACCATCACCAAC[C/G]AAAGGCAACCAGTGA	4542
rs567991191	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8536802	GATGGTCCCTTCTGG[G/T]GTCAGTTCTGCAGGT	4542
rs567997943	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8530691	CCCATCCCCACACAT[A/G]TGCTAATTTTTTTAA	4542
rs568010860	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8564440	AGAGTCCCTGGGGTG[C/T]GTCAGGAGATGACAG	4542
rs568068302	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8531118	CTTGGGAGGCTGAGG[C/T]GGGAAGATCGCCTGA	4542
rs568073112	snp	C/T	0.00279162	0.0372561	intron-variant	MYO1F	GRCh38.p7	19:8559437	TTAAATAAGCCCAGC[C/T]TTTGGCATAAGGGTA	4542
rs568087491	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	MYO1F	GRCh38.p7	19:8521078	GGCTGTGAAAACATC[A/G]TCCTTGTTGGGCACT	4542
rs568190779	snp	C/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8525627	GCCCCGCCCACAAAT[C/G]TAGTCCATTCTGAGG	4542
rs568261351	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8548405	ACACACGCCTAGCCA[A/G]CTTCATGGGTGATGT	4542
rs568278246	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8527053	TAAGGGCCAAGTCAG[C/T]GGTGACCAGGTAGGA	4542
rs568298529	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8554015	AGGCTGGAGTGCAGT[A/G]GTGTGATCATAGCAC	4542
rs568316480	snp	A/G	0.00010507	0.00724733	synonymous-codon, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526472	GCTCTTGGGCAGCCC[A/G]TCGCCCACGCTGACC	4542
rs568372510	snp	A/G	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8556780	TTATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	4542
rs568378469	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8537466	TTTTGTTTTGAGATG[A/G]AATTTTGCTCTGTCA	4542
rs568384777	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8549861	GCTGGAGTACAATAG[C/T]GCAATCATAGCTCAC	4542
rs568450203	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8570558	TTTTAGTAGAGACAG[C/G]GTTTCACCACGTTGG	4542
rs568478426	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8543559	AATTCTGTTCCCTCT[A/G]TTAGGGGAGTTGATG	4542
rs568499908	snp	A/G	0.00597247	0.0543191	intron-variant	MYO1F	GRCh38.p7	19:8538645	CAGGCTAAAGTGCCA[A/G]GGTGCAATCATGGTT	4542
rs568530224	snp	A/G	0.00517822	0.0506191	intron-variant	MYO1F	GRCh38.p7	19:8522185	CCGCCACCACGCCCG[A/G]CTAATTTTTTGTATT	4542
rs568561266	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8532672	TGGGAGCATTGTTGA[A/G]CCCAGGAGTTCAAGA	4542
rs568601174	snp	G/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8560576	GGATTTTTTTGTTTT[G/T]TTTTGGTTTGGTTTT	4542
rs568620156	snp	C/T			downstream-variant-500B	MYO1F	GRCh38.p7	19:8520316	TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT	4542
rs568633559	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8561366	TCCCTCCCTCCCTCC[C/T]TCCCTCCCTCCCTTC	4542
rs568686222	snp	C/G/T	0.00199481	0.0315187	utr-variant-3-prime, downstream-variant-500B	MYO1F	GRCh38.p7	19:8520910	GATTACAGGCGTGAG[C/G/T]CACTGCGCCCAGCCC	4542
rs568701836	snp	A/G	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8555247	TGGTGGCGCATGCCT[A/G]TAATCCCAGCTACTT	4542
rs568711578	snp	A/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8566717	TGGGGTTTCACCATG[A/T]TGGCCAAGCTGGTTT	4542
rs568808279	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8570445	GGCATGACCTTGGCT[A/C]AACCTCTGCCTCCCA	4542
rs568856066	snp	A/G	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8560959	AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTTGT	4542
rs568859085	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8543837	GTGGTGGTGGTGGTG[C/G]TGGTGGTGGTGGTGG	4542
rs568865599	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8565223	CAAGATGGGGAGACC[A/G]GATGGTTGATGAGAA	4542
rs568904371	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8524346	TCTTGAACCCAGAAG[C/G]TGGAAAGTTGCAGTG	4542
rs568905632	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8564320	CAGGAGGCAGAGGTT[A/G]CAGTGAGCCAAGATC	4542
rs568927178	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8548856	GCCTCCCAAAGTGCC[C/G]GGATTACAGGTGTGA	4542
rs569090544	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8533853	GGCCAACAGGCAGAT[A/C]AAATGTTTGAGGATG	4542
rs569093899	snp	C/T	0.00279162	0.0372561	intron-variant	MYO1F	GRCh38.p7	19:8531974	AATACAAAAGTTAGC[C/T]GGGTGTGGTGGCGCA	4542
rs569128749	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8531686	GCCACTTACTACCTG[C/T]GTGCTTTTGCAAGAA	4542
rs569132596	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8556677	TGGATCACCTGAGGA[C/T]GAGAGTTCGAGACCA	4542
rs569141442	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8553981	TGATTGACTGAGATG[A/G]GGTCTCACTCTGTTG	4542
rs569177115	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8542230	TCGTGGCTGTATCCC[A/G]GGTCAGAGGTAAGGG	4542
rs569184882	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8523353	TTTTTTACTTTTATT[G/T]GTTTATTTTGAGACA	4542
rs569303614	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8555164	TCCAGCCTGGGCAAC[A/G]AGAGCCACTCAGTCT	4542
rs569336603	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8525758	CAACACCTCACTGGC[C/G]TTGCTCTTTGGGCCC	4542
rs569345387	snp	G/T	8.28205e-05	0.00643455	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554672	GCCCTGATAGAGGTC[G/T]ATCTCACGGTCGGTG	4542
rs569369703	snp	A/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8549497	CTGACTCCATACATT[A/T]AAAAAGTTTTTATTT	4542
rs569520285	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8572421	TACAGGCACATGCCA[C/G]CCCGCTTGGCTAATT	4542
rs569523990	snp	C/T	0.00199481	0.0315187	intron-variant	MYO1F	GRCh38.p7	19:8522273	GTGATCTGCCCGCCT[C/T]GGCCTCCCAAAATGC	4542
rs569527031	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8547520	GAGGCAGGAGAATCA[C/T]TTGAACTCTGGAGGC	4542
rs569546169	snp	C/G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8548899	GGCCTTGCACCTCTA[C/G/T]TTTCTTATCTTTAAA	4542
rs569580439	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526336	CGTCTTAAAAAAACC[A/G]CAAAACTCAAAAGTC	4542
rs569596352	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8573799	AGGTTGCAGTGAGCC[A/G]AGATTGCACCACTGC	4542
rs569654397	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8564252	CAGGCGTGGTGTCAG[G/T]CGCCTGTAATCCCAG	4542
rs569819927	in-del	-/CTCT/CTCTCT/CTCTCTCTCT			intron-variant	MYO1F	GRCh38.p7	19:8553892	ACACACACACACACA[-/CTCT/CTCTCT/CTCTCTCTCT]CACTCTCTCTCTCTC	4542
rs569851138	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8544526	GCCTCCCCACAGCTC[A/G]TCAGTGCAGAGATTA	4542
rs570022220	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8562006	AGGCATGAGCCACTG[C/T]GTCTGGCCCTTCCTT	4542
rs570058768	snp	C/T	0.0193772	0.0965046	intron-variant	MYO1F	GRCh38.p7	19:8568285	AAAATTAGCCAGGTG[C/T]GGTGGCGGGCGCCCG	4542
rs570082703	snp	A/G	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8567615	TCCCACCTCGGCCTC[A/G]CAAAGTGCTGGGATT	4542
rs570138763	snp	A/C/G	0.000286857	0.0119729	intron-variant	MYO1F	GRCh38.p7	19:8555807	CTGCCCTGGGGGGTG[A/C/G]GAGGGGGGTCGGGGT	4542
rs570146163	snp	C/T	0.00318978	0.0398085	intron-variant	MYO1F	GRCh38.p7	19:8561602	CCCTCCCTCTCTTCT[C/T]TTTTTTCTTTCTCTC	4542
rs570160376	snp	C/G	7.5314e-05	0.00613607	missense	MYO1F	GRCh38.p7	19:8522730	CCCAGGGATGTGGAC[C/G]GAGGGCCCCGGGGAG	4542
rs570164828	snp	C/T	0.00358779	0.0422022	intron-variant	MYO1F	GRCh38.p7	19:8523124	GCAAGCTCCGCCTCC[C/T]GGGTTCACGCCATTC	4542
rs570201236	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8548670	CAGTGGCATGATCTC[A/G]GCTCACTGCAAGCTC	4542
rs570209179	snp	C/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8528323	CACAAGGTCAGAAGA[C/T]TGAGACCATCCTGGC	4542
rs570214337	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8543960	GTGCTGGTGGTGGTG[C/G]TGGTGGTGGTGCTGG	4542
rs570258375	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8531920	GTCAAGAGTTTGAGA[C/G]CAGCCTGGCCAACAT	4542
rs570321045	snp	C/T	0.00279162	0.0372561	intron-variant	MYO1F	GRCh38.p7	19:8551303	GTGATCTACCTGCCT[C/T]GGCCTCCCAAAGTGC	4542
rs570324532	snp	A/C	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8526153	CCAAGATGGTGAAAC[A/C]CCGTCTCTACTAAAA	4542
rs570459169	snp	C/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8554120	GTGCACCACCGTGTC[C/T]GGCTAATTATTATCT	4542
rs570473035	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8525671	CGCCCCCTCAGGCTC[G/T]CCCATTAGCACCGCC	4542
rs570544352	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8549431	ACCAGCCACCATGCC[C/T]GGCTAATTTTTGTAT	4542
rs570658171	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8544113	TCCTGGGGGGTCAGC[C/T]GGAAGGGTCTGTAGT	4542
rs570680915	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8579083	CAACGTTTGTGCTGA[C/G]ACCGGCGAGTAAGCT	4542
rs570720598	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8539190	GAGGCTGAGGCAGGC[A/G]GATCACCTGAGGTCG	4542
rs570764012	snp	C/T	0.00557542	0.0525036	intron-variant	MYO1F	GRCh38.p7	19:8564443	GTCCCTGGGGTGCGT[C/T]AGGAGATGACAGAAT	4542
rs570777133	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8573047	GGTGTGGTGGCTCAC[A/G]CCTATAATCCCAGCA	4542
rs570835103	snp	A/G	1.65603e-05	0.00287747	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8551822	TAGTAATAGTAGTCC[A/G]GTGTCATGAGGCCCA	4542
rs570837520	snp	C/G	0.00199481	0.0315187	intron-variant	MYO1F	GRCh38.p7	19:8567595	CTCCCAACCTCAGGT[C/G]ATCCTCCCACCTCGG	4542
rs570870490	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8573538	CCACCACCACCACCA[C/T]GCTATAATAACCAAC	4542
rs570873153	snp	C/T			missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554519	TCGATAAGCATGTTC[C/T]GGTACATGTTGTCCG	4542
rs570940459	snp	C/T	0.00358779	0.0422022	intron-variant	MYO1F	GRCh38.p7	19:8566813	GCCACCATAACTGGC[C/T]TTTATTTATTTTAAT	4542
rs570968144	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8527767	ACAGGTGCGCACCAC[C/T]ATGCCCAGCTAATTT	4542
rs571241741	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8543984	GTGCTGGTGCTGGTG[C/G]TGGTGGTGGTGCTGG	4542
rs571254471	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8545055	AGTGCTGGGATTACA[A/G]GCATGAGCCACCATG	4542
rs571306387	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8575163	CTCACTGCAACCTCC[A/G]CCTCCCGGGTTCAAG	4542
rs571368104	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8543756	GTGCTGGTGGTGGTG[C/G]TGGTGGTGGTGCTGG	4542
rs571401283	snp	A/G	0.00279162	0.0372561	intron-variant	MYO1F	GRCh38.p7	19:8528576	CAAAAAAACAAAAAA[A/G]AAAAACAAAAAAGAA	4542
rs571412219	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8557686	GATGCCAGGCTTGGC[A/G]GGCAGGGCACAGAGT	4542
rs571466730	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8568952	CAAATGGATTCCATA[A/G]TGACCCTTGTGTGGG	4542
rs571484139	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8558632	TGTCTCTATTCAACA[C/T]ATCTCTGCAAAGGAG	4542
rs571530321	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8543014	ATTCAAGTGATTCTC[C/T]TGCCTCAGCCTCCTG	4542
rs571545906	in-del	-/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8564866	CAACCTCCGCCTCCC[-/G]GGTTCAAGTGATTCT	4542
rs571592961	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8576851	CAACTGAAAGACCCC[C/T]GAAGAGCAACTTCCG	4542
rs571617491	snp	A/G	1.65756e-05	0.00287881	intron-variant	MYO1F	GRCh38.p7	19:8551997	CCCCGCTGGGCTCCA[A/G]GTGGTGCTCCCTCTC	4542
rs571632602	snp	A/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8576152	CAGGCGTGTGCCACC[A/G]CGCCCAGTTAATTTT	4542
rs571647139	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8556847	AGCCGAGATTGTGCC[A/G]TTGCACTCCAGCCTT	4542
rs571781107	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8546383	TTTTTTTTTTGAGAC[C/T]GGGTTTTGCTCTGTT	4542
rs571800930	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8573184	GGCATGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT	4542
rs571833605	snp	C/T	0.00318978	0.0398085	intron-variant	MYO1F	GRCh38.p7	19:8572639	TCCTGTCCATCCTCA[C/T]GGCCACTGATTCTGG	4542
rs571838956	snp	A/G	0.00199481	0.0315187	intron-variant	MYO1F	GRCh38.p7	19:8569134	TGAAGTCCTATTGGG[A/G]TGAGACTGCCCCCTG	4542
rs571859177	snp	C/G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8567025	TATCCTTTCAACACA[C/G/T]GCTGGCTGAGGTTAG	4542
rs571887000	snp	C/G			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8579404	GGCAACATAGCAAGA[C/G]CTCGTCTCTACAAAA	4542
rs571928463	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8541636	GTTTTGCCATGTTGC[C/T]CAGGCTGGTCTCAAA	4542
rs571928589	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8535816	TCCTGAGTAGCTGGG[A/G]CCACAGGTGCCCGCC	4542
rs572053502	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8532763	GGTGATGGCACGCAT[A/G]TGTAGTCCCAGCTAT	4542
rs572162318	snp	A/C	0.00597247	0.0543191	intron-variant	MYO1F	GRCh38.p7	19:8532949	ACACACACACACACA[A/C]AATTGGGCTTTATTT	4542
rs572221976	snp	C/T	0.00199481	0.0315187	intron-variant	MYO1F	GRCh38.p7	19:8561717	CTCCTTTTTTTCTAT[C/T]TTTTTTTTTGTTTGT	4542
rs572300208	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8546499	CGAGTAGCTGGGACC[A/G]TAGGAGCACACCACC	4542
rs572318412	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8561087	TGGTCTTGCTCTGTT[C/G]CTCAGGCTGATGTCT	4542
rs572340294	in-del	-/A	0.00075225	0.0193794	intron-variant	MYO1F	GRCh38.p7	19:8550741	TGAATCCTGGCCTCC[-/A]ACCTGCCTCCAGGGG	4542
rs572388534	snp	A/G	1.74579e-05	0.00295443	intron-variant	MYO1F	GRCh38.p7	19:8555839	AGCCCTTGCACGGGG[A/G]TGCGGCACCTGGCTC	4542
rs572465838	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8550969	CACTGCAACCTCCTC[A/C]TCCCAGGTTCAAGCG	4542
rs572482877	snp	C/T			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8579333	CCTGTAATCCCAGAA[C/T]TTTGGGAGGCTGAGG	4542
rs572488649	snp	A/C	0.00318978	0.0398085	intron-variant	MYO1F	GRCh38.p7	19:8523247	ATCATGTTAGCCAGG[A/C]TGGTCTCGATCTCCT	4542
rs572491331	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8562876	GTTGAAAGTCATGCC[A/G]GTGGTGGCGTTAAAA	4542
rs572499995	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8575493	CTGAGAGGAGGTGGA[A/G]CTCGGGCTTGCTTGC	4542
rs572545916	snp	C/T	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8545175	TCACTGCACCCTTGA[C/T]TTCCTGGGCTCAAGT	4542
rs572573901	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8550508	CTGAGCTAGGAGGAC[A/G]CAGTTCACCCACCCA	4542
rs572610322	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8534428	TTCTCCTGCCTCAGC[A/C]TCCCAGGTAGCTGGG	4542
rs572648482	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8523325	GGCATGAGCCACCGC[A/G]CCTGGCCAATTATTT	4542
rs572676248	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8574898	GTAGCTGGGGTTACA[A/G]GCGCGCACCACCACG	4542
rs572767515	snp	A/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8541468	GAATCTCCCTCTGTC[A/G]CCCAGGCTGGAGTGC	4542
rs572782341	snp	C/T	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8529541	ACTAGGCTGCCTGGG[C/T]CAGGTGAGAGTGTAC	4542
rs572831303	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8557320	AAAAAGTTTTGAGAC[A/G]GGGTCTCACTCTGTC	4542
rs572832100	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8562191	TATTTTTAGTGGAGA[C/T]GAGGTTTCACCGTGT	4542
rs572899964	snp	C/G	0.00597247	0.0543191	intron-variant	MYO1F	GRCh38.p7	19:8541778	AGAAACACCATCCTG[C/G]CCGCACAGCCACTCC	4542
rs572911063	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8556697	GTTCGAGACCAGTCT[C/G]ATCAATATGGAGAAA	4542
rs572992346	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8562623	TAACTGTAGCCTTGA[C/T]GTCCAGGCTCAAGTG	4542
rs572994174	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8551540	TATTTTAAGTAGAGA[C/T]GGGGTTTAACCACGT	4542
rs573032298	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8557919	ACCTCTCCTCTTCTC[C/T]TGTGGTCACACATAC	4542
rs573054515	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8564065	CGGGATTTAAAGGAG[A/G]CCTAATTAGGTGTTT	4542
rs573120483	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8576262	TCTCAGCCTCCTAAA[A/G]TGCTGGGATTACAGG	4542
rs573184905	in-del	-/A	0.00159617	0.0282053	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578410	TCCCAAAGTGCTGGG[-/A]TTACAGGCATAAGCC	4542
rs573248456	snp	C/T	0.000100637	0.00709285	missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536358	TGGCGTTCGTCCCCA[C/T]GCCACCGCGGCCACG	4542
rs573277150	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8570671	AGCCACCGCACCCAA[C/T]CACATTTTTTTTTTT	4542
rs573282589	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8528136	CTGAGACAGGAGAAT[C/T]GCTTGAACCCAGGAG	4542
rs573315670	snp	C/G	0.0023933	0.0345097	intron-variant	MYO1F	GRCh38.p7	19:8577113	CTGGCATCCCCACCA[C/G]CTACAGATGGGAGCT	4542
rs573439055	snp	A/G	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8553022	GAGTAGGTATTTCCT[A/G]CTGGGTTTTCAATGG	4542
rs573443839	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8528741	GAAAGTACTTGGGTC[A/G]TGTGACTGTAGCCAG	4542
rs573460744	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8524515	GCTTGAACCCAGGAG[G/T]TGGATGTTGCAGTGA	4542
rs573540688	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8567853	GATGGGTCATGTCTA[C/T]AATTTCCCCTTTGGG	4542
rs573549383	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8556650	CCCAGCACTTTGGGA[A/G]GCCAAGACGGGTGGA	4542
rs573565840	in-del	-/A	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8561257	TGGGGAAAGGTGTGG[-/A]GGTGTGGCTGCAGCA	4542
rs573627624	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8525001	TCAGGAGTTCGAGAC[C/T]AGCCTGAACAACGTG	4542
rs573639030	snp	A/G	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8562151	GCCGTTCTCCTGCCC[A/G]GCTAATTTTTTCTTT	4542
rs573738667	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8543864	GTGGTGGTGCTGGTG[C/G]TGCTGGTGGTGCTGG	4542
rs573787779	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8576204	AGGTTTCACCACGTT[G/T]GCCAGGCTGGTCTCG	4542
rs573835355	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8579054	GGCCATCAGGGGAGG[C/G]TTCTAGGAAGAGGCA	4542
rs573850750	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8569999	CAGCCTTGACCTCCC[A/G]GGCTCAAGCGAATCC	4542
rs573896995	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8529402	GGTGATTAGAGTACA[C/T]GTAGGTTCAGGGCTG	4542
rs573976867	snp	A/G	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8556384	CAGTGGCTCATGCCC[A/G]TAATCCCAGCACTTC	4542
rs574014272	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8575504	TGGAGCTCGGGCTTG[C/T]TTGCCTGCCACTCAT	4542
rs574031040	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8541356	AACCACATGTCAAAC[A/G]CTTTAAGGATCCCCG	4542
rs574092908	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8527773	GCGCACCACCATGCC[C/T]AGCTAATTTTGGTAT	4542
rs574109831	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8566514	TATTTATTTAATTTA[A/G]TTAATTTATTTATTT	4542
rs574133771	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8535371	CAAAATCTATAGACT[G/T]AAATTTTTGTCTAAA	4542
rs574190228	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8535884	GACGCGGTTTCACTG[C/T]GTTAGCCAGGATGGT	4542
rs574259924	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8563999	AGGCAATCACATTGA[C/T]TCTTTTTGAAACTAT	4542
rs574298825	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8529782	GTTTGATGGACAGCT[A/G]TGTCTGCTATACTTG	4542
rs574421912	snp	C/T	0.00199481	0.0315187	intron-variant	MYO1F	GRCh38.p7	19:8558721	TCAGATAAGATGTCT[C/T]TCCTCCTGGAAGCCC	4542
rs574428516	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8523898	GGCTAAGGTGGGCTG[A/G]TCACGAGGTCTGGAG	4542
rs574468128	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8531730	ACGGTTTCTTACACT[A/G]TTACTCGACACTATC	4542
rs574491269	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8524372	CAGTGCGCTGAGACC[A/G]CACCATTGCACCCCA	4542
rs574507220	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8531288	GGAGTTGGAGGTTGC[A/G]GTGAGCTGAGATTGT	4542
rs574514704	snp	C/G	0.000420588	0.0144954	intron-variant	MYO1F	GRCh38.p7	19:8577275	GTGTCCCTCCTCTTT[C/G]TTCTTCCAGATCCCA	4542
rs574523880	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8552338	ATGTCGGCTCACTGC[A/G]ACGTCCACCTCCTGG	4542
rs574535196	snp	C/T	1.66846e-05	0.00288826	synonymous-codon, missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536543	GTAGGCGAAGCCGGC[C/T]CTGCGCACCCTGATG	4542
rs574558870	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8547387	GAGGTGGGTGGATCA[C/T]GAGGTCAGGAGTTTG	4542
rs574563469	snp	C/T	0.00438332	0.0466095	intron-variant	MYO1F	GRCh38.p7	19:8542310	TCAGAGGCCGGGGGG[C/T]GGTGAAAGTTATAGC	4542
rs574597769	snp	G/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8552926	GAATGTTACACAGGG[G/T]TGTCATGGCCTCCAC	4542
rs574598368	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8536171	TGTCTCCCTCTGTCT[C/T]TCTCTCTCTCTCTCA	4542
rs574631560	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8525924	TCCTTGCTGTTGCCC[C/T]CTCTGGTCCAGCCTG	4542
rs574676650	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8548134	TTTTCTGCAGAAGGA[A/G]GAAAAGGGTCCTTCC	4542
rs574721871	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8547931	AGAGAGGTGGGAACG[C/T]GGTGGGGAGGGCTGG	4542
rs574754559	snp	A/G	0.00279162	0.0372561	intron-variant	MYO1F	GRCh38.p7	19:8549025	GCGCAATCTCGGCTC[A/G]CTGAAACCTCTGCCT	4542
rs574793306	snp	A/G	0.00318978	0.0398085	intron-variant	MYO1F	GRCh38.p7	19:8548640	GAGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTGC	4542
rs575144489	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8524796	TGTGGGTACGTCTTG[A/G]TGGATAAATAAGAGC	4542
rs575154410	snp	G/T	0	0	intron-variant	MYO1F	GRCh38.p7	19:8523330	GAGCCACCGCGCCTG[G/T]CCAATTATTTTTTAC	4542
rs575214542	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8530766	AAAAAGGGGCCGGGC[A/G]CAGTGGCTCACGCCT	4542
rs575338927	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8541539	GTTCAAGAGATTCTT[A/G]TGCTTCCACCTCCTG	4542
rs575357287	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8557346	CTGTCACCCAGGCTG[C/G]AGTGCAGTGGTGTGA	4542
rs575374449	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8531237	CTGTAATACCAGCTA[C/T]TCAGGAGGCTGAGGC	4542
rs575391365	snp	C/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8547184	TGTGTGCCTGCGGTC[C/T]CAGCTACTTGAGAGG	4542
rs575417254	snp	C/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8558059	CCCTGCTGCCCCTGC[C/T]GTGGCCTTCTCCTCT	4542
rs575503603	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8554280	CATTTAGAGGGGACA[G/T]ACAGACAATAGCAGA	4542
rs575506601	snp	A/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8571005	ATGCTAGCGTTCCTC[A/T]CTGTCCCCATCAATG	4542
rs575539877	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8560259	GGAGGCTGAGGCGGG[C/T]GGATCATGAGGTCAG	4542
rs575541675	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8553728	AATACAAAAATTAGC[C/T]GGACATGGTGGTGGG	4542
rs575602558	snp	A/G			downstream-variant-500B	MYO1F	GRCh38.p7	19:8520577	GGATTACAGGTGTGA[A/G]GCACCGCGCCCACCT	4542
rs575667361	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8577629	ACTCCTTGGGGACAG[A/G]GCTGCTGCAGGAACA	4542
rs575765746	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578390	GTGATCCTCCCAACT[C/T]GGCCTCCCAAAGTGC	4542
rs575777950	snp	A/G	0.00557542	0.0525036	utr-variant-3-prime	MYO1F	GRCh38.p7	19:8521386	GTGACCCAGGGCCTG[A/G]GCAGGACTGGAGGCC	4542
rs575779374	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	MYO1F	GRCh38.p7	19:8521241	AAGACCCATTTCTTA[A/G]TCACATGGCAGTTGG	4542
rs575790692	snp	A/T	0.00597247	0.0543191	intron-variant	MYO1F	GRCh38.p7	19:8572614	TAAATTCCTTTTGAC[A/T]CCCAGCCTTTCCTGT	4542
rs575808820	snp	A/G/T	4.96827e-05	0.0049839	intron-variant	MYO1F	GRCh38.p7	19:8545621	GGGGACCAGTGAGAC[A/G/T]CCCCCGCCAAAGTTG	4542
rs575895769	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8521684	CTGTCCATCTTGTTC[A/G]TGGGGACTCCCTATG	4542
rs575942319	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8552688	AACTCAGGAAGTTGC[A/G]TAGATTTTTTTCCCC	4542
rs575970068	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8544018	TGGCGGTGGCGGTGG[C/T]GGTGGCGGTGGCGGT	4542
rs575981422	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8543060	AGGTGCCCACGACCA[C/T]GCCCGGCTGATTTTT	4542
rs576021345	snp	C/T	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8548585	AACCTCTCTGCACCT[C/T]TATTTTCTTTTTTTT	4542
rs576035697	snp	A/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8560065	TCACACCATCTCAGT[A/G]TGGGTAGGCTCGAAG	4542
rs576137126	snp	A/T			intron-variant	MYO1F	GRCh38.p7	19:8574957	GACAGGGTTTTGCCA[A/T]GTTGGCCAGGCTGGT	4542
rs576156790	in-del	-/A			intron-variant	MYO1F	GRCh38.p7	19:8534178	AGCGAGACTCTGTCT[-/A]AAAAAAAAAAAAAAA	4542
rs576210617	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8532704	CAGCCTGGGCAACAT[A/G]GAAAGACCCCGTCTC	4542
rs576218913	in-del	-/T			intron-variant	MYO1F	GRCh38.p7	19:8575078	TAGATTTTCTTTTTC[-/T]TTTTTTTTTTTTTTT	4542
rs576244272	snp	G/T	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8567000	GCTTTTTATGTGAAT[G/T]ACTTCATCTTATCCT	4542
rs576273472	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8560732	AGGCACATGCCACCA[C/T]GCCTGGCTAATTTTT	4542
rs576396418	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8552752	ACCCTGAATCCATAT[C/T]TGTTTACCTATCCTG	4542
rs576408954	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8561034	GAGCCACTGCGCCTG[A/G]CCACGCCTGGCTAAT	4542
rs576476981	snp	A/G	0.0023933	0.0345097	intron-variant	MYO1F	GRCh38.p7	19:8558748	GCCCCCCATCCCCAG[A/G]CCAGGAGCTCCTGGA	4542
rs576551891	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8545083	ATGTCCCGCCTAAAT[A/G]CGTCTTAAATTTAAT	4542
rs576553361	snp	C/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8554949	AGCACTTTGGAAGGC[C/T]GAGGCAGGCGGATCA	4542
rs576568797	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8539136	AATACAAAATTAGGC[C/T]GAGCGCGGTGGCTCA	4542
rs576603788	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8544692	GCTACTGTGGAAGCT[C/T]GCTGAGGTGCAGAAG	4542
rs576613475	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8539527	CTTGAACCCAGGAGG[C/T]GGAGGTTGCAGAGGG	4542
rs576804708	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8574147	ACAATCCACCACCAA[C/G]GAACAACATTAAACA	4542
rs576814588	snp	G/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8521905	AGTGATCCTCCTGCC[G/T]CAGCCACTGAAAGTG	4542
rs576829763	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8548465	TTTAGCTCTGCCCTT[C/G]CTGGCTCTGTGTACA	4542
rs576863075	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8577801	CCAAGGTTGGAGGAT[C/T]GCTTGAGTCCAGGAG	4542
rs576900447	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8573493	AGCAATTCCAGCATC[A/G]GCCTTCCTTACATTC	4542
rs576916415	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	MYO1F	GRCh38.p7	19:8521164	GAATGAGCAAAGTCA[C/T]GCTTGTTAAGGACCC	4542
rs576967984	snp	C/T	0.00199481	0.0315187	intron-variant	MYO1F	GRCh38.p7	19:8522212	TATTTTTAGTAGAGA[C/T]GGGGTTTCACTGTGT	4542
rs577093062	snp	A/C	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8544599	GGGGTGGGGAGGGCA[A/C]CAGGGGCTTCAAATA	4542
rs577107979	snp	A/C	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8537634	AGACAGGGTTTTGCC[A/C]TGTTGGTCAGGCTGG	4542
rs577126101	snp	A/G	1.69467e-05	0.00291085	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544355	TTGAAATGCTCGTGG[A/G]TCCCCACAGCCGCCT	4542
rs577143135	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8537082	GTGAAGACGGGTGGG[G/T]GGGGGGCACAGAGAT	4542
rs577143274	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8542899	TGAGCCACTGCACCC[A/G]GCCCTGTTTGCTTTT	4542
rs577155948	snp	C/T	0.000798403	0.0199641	synonymous-codon, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526496	GCTGACCGTGAGGGT[C/T]CGACCGCCAACCTTG	4542
rs577248457	snp	C/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8554911	AGGGCTGGCCGGGCG[C/T]GGTGGCTCATGCCTG	4542
rs577408249	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8555306	ATCCGGGAGGTGGAG[A/G]TTGCAGTGAGCTGAG	4542
rs577432847	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8560688	CAAGTGATCCTCCTG[A/G]TCTCAGCCTCCTGTG	4542
rs577461683	snp	C/T	0.00557542	0.0525036	intron-variant	MYO1F	GRCh38.p7	19:8561784	TGTAGTGGCGCGATC[C/T]TGGCTCACTGCAAAA	4542
rs577473392	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8549710	GGGTTTCACCATGTT[G/T]GCCAGGCTGGTCTCA	4542
rs577477183	snp	C/T	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8568417	GAAAGAGTGAGACTC[C/T]GTCTCAAAAAAAAAA	4542
rs577485957	snp	A/G	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8556526	AGAAAGAGAAAGAAA[A/G]AAAGAAATGAGATCT	4542
rs577516256	snp	C/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8548839	GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAGTGC	4542
rs577516290	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8571229	TAGCTGCTTCTGGAG[A/C]CAGCTCTCAGCTCCC	4542
rs577523288	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8555905	CCCCCGCCCCACCTC[C/T]ATTCCTCCTTCCCCA	4542
rs577527134	snp	C/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8573208	CCCAGCTACTCGGGA[C/G]GCTGAGGCAGGAGAA	4542
rs577625281	snp	A/G	0.00159617	0.0282053	intron-variant	MYO1F	GRCh38.p7	19:8527536	CTGGCCAGCCTGGCC[A/G]CAGAGGATCCACCCC	4542
rs577687594	snp	G/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8574084	CAGCAACCACCGATG[G/T]TCATCATTCCACTGG	4542
rs577776560	snp	A/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8575472	TCTAATGGCGCCCCC[A/G]AGAATCTGAGAGGAG	4542
rs577781244	snp	C/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8528096	GCGAGGTGGTGGGCA[C/T]CTGTAGTCCCAGCTA	4542
rs577801325	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8541246	TGCTATGTTGCCCAG[G/T]CTGGTCTTAAACTTG	4542
rs577838846	snp	C/T	1.65666e-05	0.00287802	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550583	CACTCTCCACTCGGG[C/T]GTAATTCCCGTCTTC	4542
rs577854357	in-del	-/AATTACTT	0.00199481	0.0315187	intron-variant	MYO1F	GRCh38.p7	19:8566997	TAAGCTTTTTATGTG[-/AATTACTT]CATCTTATCCTTTCA	4542
rs577857552	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8525142	GAGGTGAAGGTTGCA[G/T]TGAACCGAGATCGCT	4542
rs577898623	snp	C/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8522925	GCTGAGGGAGGAGAC[C/T]GCGACACTCTCAACC	4542
rs577918202	snp	A/T	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8523204	GCCTGGATAATTTTT[A/T]AAATATTTTTAGTAG	4542
rs577919221	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8543685	TGGTGCTGGTGGTGG[C/T]GGTGGTGGTGGTGGT	4542
rs578152905	snp	A/G	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8529707	AATGTGTGATTGTTG[A/G]GAGATGCATCTGGCC	4542
rs578174420	snp	A/G	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8562739	GGGTCTCCCTATGTT[A/G]CCCAGGCTGGTCTCT	4542
rs578201805	snp	G/T	0.000399281	0.0141238	intron-variant	MYO1F	GRCh38.p7	19:8569321	GAGCTCTTGTGAAAG[G/T]CAGTCAGGGGCTTGA	4542
rs578233030	snp	G/T	0.000798403	0.0199641	intron-variant	MYO1F	GRCh38.p7	19:8540438	AATAAGGCCGGGTGC[G/T]GTGGTGCATGCCTGT	4542
rs578250022	snp	C/G	0.00119737	0.0244387	intron-variant	MYO1F	GRCh38.p7	19:8524702	AGTGCTTGGATTACA[C/G]GTGTGAGCCATCTTG	4542
rs745372109	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8554922	GGCGCGGTGGCTCAT[A/G]CCTGTAATCCCAGCA	4542
rs745398695	snp	C/G	1.71843e-05	0.00293119	intron-variant	MYO1F	GRCh38.p7	19:8547998	TCCACCCCACCCCCA[C/G]CCCAGGATCCCCCAT	4542
rs745399653	snp	C/T	4.9708e-05	0.00498513	intron-variant	MYO1F	GRCh38.p7	19:8551922	CTTGCCTGGCTCAGC[C/T]CCTGTGATCCCTCAT	4542
rs745432463	snp	A/G	2.0479e-05	0.00319986	intron-variant	MYO1F	GRCh38.p7	19:8522571	CAGGGGGTTTGAGTC[A/G]CAGCCCCAGACACTC	4542
rs745445244	snp	C/T	1.67747e-05	0.00289605	missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536374	GCCACCGCGGCCACG[C/T]CTCGGGGGTCAGAAT	4542
rs745498918	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8522975	CCAGACGGAGGGACT[A/C]TGCCGCTAGGAGGGC	4542
rs745501458	snp	A/G	1.65649e-05	0.00287788	intron-variant	MYO1F	GRCh38.p7	19:8554622	GGGCCAGGAGTCTGG[A/G]GGCTGTGCCTCCCAC	4542
rs745536156	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8540419	TGTACATTTTAAAAT[G/T]GTTAATAAGGCCGGG	4542
rs745550894	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8562562	TTTTTTTGAGGCAGG[G/T]TCTTGCTCTGTTGCC	4542
rs745551971	in-del	-/C	6.63636e-05	0.00575998	intron-variant	MYO1F	GRCh38.p7	19:8545788	AAAAAGTTGTGGCCA[-/C]CCTTCCCCCCATGTC	4542
rs745590765	in-del	-/C	2.05282e-05	0.0032037	intron-variant	MYO1F	GRCh38.p7	19:8522575	GGGTTTGAGTCACAG[-/C]CCCAGACACTCCCCT	4542
rs745602882	snp	C/G/T	8.28005e-05	0.00643383	synonymous-codon, missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8551782	GTCCGTGCCGTCCAC[C/G/T]TGGTAGGTGTCCGAT	4542
rs745609674	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8568626	CTCAGTTTCTCCTCT[G/T]TGCAAGTGGATTTGG	4542
rs745628377	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8562430	CTCCTGCCTTGACCT[C/T]CTGAGTAGCTGGGCC	4542
rs745641070	snp	G/T	0.000152072	0.00871854	missense	MYO1F	GRCh38.p7	19:8525533	ACGACCTCCGAGGTT[G/T]TCCCTTGGCCATTCC	4542
rs745692023	snp	C/T	2.03614e-05	0.00319066	utr-variant-3-prime	MYO1F	GRCh38.p7	19:8521478	GGCTCCCCACCAGGC[C/T]GGCAGGCAGATAGGC	4542
rs745695943	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8567491	CTCCTGCCTCAGCCT[C/G]TTGAGTAGCTGGGAT	4542
rs745759162	snp	A/G	1.65638e-05	0.00287778	synonymous-codon, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530298	CTCCAGCCCCAGGTA[A/G]TCCCCGACGAAGTTC	4542
rs745812373	snp	C/G	1.65732e-05	0.00287859	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530428	AGGTCCTTGTGCCCC[C/G]ACCCCGCGCCGTTTA	4542
rs745825629	snp	C/G/T	0.000201876	0.0100449	synonymous-codon	MYO1F	GRCh38.p7	19:8525483	CAGCTCCTCACCTCT[C/G/T]GGGGGCGCAGGGGCC	4542
rs745829503	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8529590	GGGCCAGGTGAAGGT[A/G]TATCTAATTTCCAGG	4542
rs745838171	snp	C/G	1.67192e-05	0.00289125	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550214	GGCCAGGGCATCACG[C/G]GTGTAGGCTGCCTGC	4542
rs745850328	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8571987	CTCGGCCTCCTAAAG[G/T]ATTGGGATTACAGGC	4542
rs745871661	in-del	-/TC			intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8536168	CTCTGTCTCCCTCTG[-/TC]TCTCTCTCTCTCTCT	4542
rs745879013	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8561778	CTGGAGTGTAGTGGC[A/G]CGATCTTGGCTCACT	4542
rs745925360	snp	A/G	3.33317e-05	0.00408224	intron-variant	MYO1F	GRCh38.p7	19:8522328	CGCCCGGCCGATGTC[A/G]GGGTTCTTACCACTC	4542
rs745930357	snp	A/G	4.48159e-05	0.00473349	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526609	ACTGTAGTCTATGGG[A/G]AGAGAAGAAAGCTTG	4542
rs745936980	snp	A/C	1.65611e-05	0.00287755	intron-variant	MYO1F	GRCh38.p7	19:8545604	CTTCCAGACTCAGCT[A/C]AGGGGACCAGTGAGA	4542
rs745975606	snp	C/T	3.32441e-05	0.00407688	intron-variant	MYO1F	GRCh38.p7	19:8555596	CTTCACCCTCCTCTC[C/T]GTCCATGGCCCAGCC	4542
rs745998387	in-del	-/T			intron-variant	MYO1F	GRCh38.p7	19:8541426	GTGTGTGTGTGTGTG[-/T]TTTTTTTTTTTTTTT	4542
rs746004780	snp	A/G	1.66418e-05	0.00288455	synonymous-codon	MYO1F	GRCh38.p7	19:8522402	GATCTCAATGACCTC[A/G]TTCACGTTGAAGCTC	4542
rs746044356	snp	C/T	3.31466e-05	0.0040709	intron-variant	MYO1F	GRCh38.p7	19:8550544	CTCCATCCAGCCCTC[C/T]CTGATACCCACACTC	4542
rs746093528	snp	C/T	7.89422e-05	0.00628211	missense, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526500	ACCGTGAGGGTCCGA[C/T]CGCCAACCTTGAGCA	4542
rs746128755	snp	C/G/T	0.000202964	0.0100722	intron-variant	MYO1F	GRCh38.p7	19:8544468	GCCTGGGGGGCTCTG[C/G/T]GGGGCGAGCGGGAGC	4542
rs746130751	snp	A/G	1.65718e-05	0.00287848	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550633	AGGTGCAAGATCCCC[A/G]CCACGAGCTGCAGGA	4542
rs746157840	snp	A/T			intron-variant	MYO1F	GRCh38.p7	19:8550000	GATGGGGGTCTTGCT[A/T]TGTTGCCCAGGCTGG	4542
rs746168641	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8538065	CAACCTCCGTCTCCC[A/C]GGTTCAAGTGATTCT	4542
rs746204991	snp	C/T	1.66674e-05	0.00288676	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8530524	GCCTTCTGGATGGTT[C/T]GGGCAAAGCCATCGA	4542
rs746208713	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8547891	CAGAAGGAAGTATCA[A/C]TATGGAGCCTGGGTA	4542
rs746240186	snp	C/T	1.67492e-05	0.00289384	intron-variant	MYO1F	GRCh38.p7	19:8541877	TTGGGGGGTTGTAGC[C/T]GGAGGTCCCCATGCC	4542
rs746250683	snp	A/G	1.65231e-05	0.00287424	intron-variant	MYO1F	GRCh38.p7	19:8553316	CATGCAGGTGAGGGC[A/G]ACCCAGCTTATCCTT	4542
rs746252838	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8569114	TGAATGAATGAATGA[A/G]TGAATGAAGTCCTAT	4542
rs746319059	snp	A/G	1.65649e-05	0.00287788	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8548091	AGCTTCTCATTGACG[A/G]AGTTGATGCAAAACT	4542
rs746324005	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8549404	GCCTCCTGAGTAGCC[A/G]GGATTACAGGCACCA	4542
rs746383576	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8522979	ACGGAGGGACTCTGC[C/T]GCTAGGAGGGCCTAG	4542
rs746419861	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8558995	GCGAGCCTGTCACCT[C/T]GGCCTCCTGAGTAGC	4542
rs746445944	in-del	-/C	1.6571e-05	0.0028784	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530417	ACAGCTCCTCCAGGT[-/C]CTTGTGCCCCCACCC	4542
rs746455069	in-del	-/AA/AAA			intron-variant	MYO1F	GRCh38.p7	19:8524118	GCAAGACACCGTCTC[-/AA/AAA]AAAAAAAAAAAAAAA	4542
rs746597787	snp	G/T	0.000174526	0.00933984	intron-variant, missense, utr-variant-3-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536611	CTCTGGTGGGGAGGG[G/T]AGGCTGAGTCCCCTC	4542
rs746612697	snp	A/C	1.65754e-05	0.00287879	intron-variant	MYO1F	GRCh38.p7	19:8551931	CTCAGCCCCTGTGAT[A/C]CCTCATCTGCCCTGC	4542
rs746649143	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8533817	GACTATTATAACATA[C/T]CTGGGATGCTGGGCC	4542
rs746682055	snp	A/G	1.75293e-05	0.00296046	intron-variant	MYO1F	GRCh38.p7	19:8527488	CGCTTGATGGGCTGT[A/G]GGGATGCAGGATTAG	4542
rs746703051	snp	C/G	1.65831e-05	0.00287945	intron-variant	MYO1F	GRCh38.p7	19:8551982	CCTTCCCATTGTCCA[C/G]CCCGCTGGGCTCCAG	4542
rs746704714	snp	A/G	3.31257e-05	0.00406962	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8548111	GATGCAAAACTGCTC[A/G]AAGCCATTTTTCTGC	4542
rs746722066	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8545571	GGATGCCATAACACC[C/G]TTGGCCCTCCCCCTC	4542
rs746766742	snp	A/T	1.67452e-05	0.0028935	missense	MYO1F	GRCh38.p7	19:8521556	ACGTAGTTTCCTGGG[A/T]AAAGGCCCTCCTGGC	4542
rs746781293	snp	C/G	1.65671e-05	0.00287807	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554693	ACGGTCGGTGAAGTA[C/G]GGCATCTGCTTGAAG	4542
rs746792025	snp	A/G/T	0.000100082	0.00707335	missense, synonymous-codon, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536514	CTCTGCAGGAATTTG[A/G/T]CGAACTGGCGGCGGT	4542
rs746802189	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8574455	ACCGGTTTAATGGAA[A/G]ACAATTTTTCCATGG	4542
rs746849588	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8545232	AGCTGGGATTACAGG[C/T]GCCTGCCACCACGCC	4542
rs746878813	in-del	-/TTTA			intron-variant	MYO1F	GRCh38.p7	19:8540340	TTCATTTTATCTTAT[-/TTTA]TTTATTTATTTATTT	4542
rs746897022	snp	A/C	1.70449e-05	0.00291928	missense	MYO1F	GRCh38.p7	19:8525542	GAGGTTTTCCCTTGG[A/C]CATTCCCTTCCGCGT	4542
rs746912834	snp	G/T	1.66029e-05	0.00288117	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8530486	TCTCCTCGTACTTCC[G/T]GACAGCCACGTGGCG	4542
rs746916738	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8554609	AGCCCAGGGCTGGGG[G/T]CCAGGAGTCTGGGGG	4542
rs746924954	snp	G/T	1.85324e-05	0.00304399	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550321	CCTGCAGTCGCCCGC[G/T]GTCAATGCCCAGCAG	4542
rs746935826	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8528555	CAAAAGAGCAAAACT[C/T]TGTCTCAAAAAAACA	4542
rs746950086	snp	A/C	2.06644e-05	0.0032143	intron-variant	MYO1F	GRCh38.p7	19:8525602	GAATGACAGACAGAC[A/C]ACGCTCTTTGCCCCG	4542
rs747040239	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8558960	CACGGCTCACTGCTA[C/T]CTCTGCCTGCGGGGC	4542
rs747069795	snp	C/T	1.71832e-05	0.00293109	synonymous-codon	MYO1F	GRCh38.p7	19:8522477	CCTGGGACCATGTGT[C/T]CGAGGCTGGGGCTTG	4542
rs747086449	snp	A/G	3.4191e-05	0.00413453	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8537010	TGCAGCGGATGTAGT[A/G]GGGTGTGCACCTCAT	4542
rs747132625	in-del	-/TTCTTCTCTCTCA			intron-variant	MYO1F	GRCh38.p7	19:8561498	TTTCTTTCGTTCTCT[-/TTCTTCTCTCTCA]TTCTTCTCTCTTTCT	4542
rs747145836	in-del	-/TTTA			intron-variant	MYO1F	GRCh38.p7	19:8540343	TTTTATCTTATTTTA[-/TTTA]TTTATTTATTTATTT	4542
rs747155271	snp	A/G	1.6693e-05	0.00288898	intron-variant	MYO1F	GRCh38.p7	19:8550729	GAAACTGTGCCGTGA[A/G]TCCTGGCCTCCAACC	4542
rs747165118	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8549020	CAGTGGCGCAATCTC[A/G]GCTCACTGAAACCTC	4542
rs747216890	snp	A/C			utr-variant-3-prime	MYO1F	GRCh38.p7	19:8521179	CGCTTGTTAAGGACC[A/C]CCCCCTCCCCAACTG	4542
rs747249123	snp	A/G	1.65644e-05	0.00287783	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555698	CTTCCGGAGGTTGGC[A/G]GCAATGGCGTCTTCG	4542
rs747278790	snp	A/G	1.6759e-05	0.00289469	intron-variant	MYO1F	GRCh38.p7	19:8536923	GCCTGGGGGGAATGA[A/G]TCTTGGATTGGTTGG	4542
rs747311306	snp	A/G	1.65608e-05	0.00287752	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8552083	TTTGCATGACCACGC[A/G]GGACTTCTCCAGCAA	4542
rs747314837	snp	A/G			intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8529992	CTGTGCCAGGTGAGG[A/G]TATACCTGTGATGGA	4542
rs747358534	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8550849	CGCGTGACCTTGGGT[A/G]AGTGCCTGCACCTCT	4542
rs747364980	snp	A/G	5.02155e-05	0.00501051	synonymous-codon, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536303	CATCTGGTACTGGTC[A/G]GGCTCCATGTTGACC	4542
rs747378295	snp	A/G	5.95965e-05	0.00545845	synonymous-codon, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526523	CTTGAGCACTGCCAA[A/G]TCGCCGAAGCCGCGG	4542
rs747404703	snp	C/G	1.67377e-05	0.00289284	intron-variant	MYO1F	GRCh38.p7	19:8541890	GCCGGAGGTCCCCAT[C/G]CCTGGGACCACTCAC	4542
rs747431464	snp	C/T	8.07657e-05	0.00635424	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526646	CTGGCTGAGGTCCCC[C/T]GCCCCACCCAACTCT	4542
rs747571133	snp	C/G	6.76293e-05	0.00581464	intron-variant	MYO1F	GRCh38.p7	19:8542002	GAGACCTGGAGGGGA[C/G]AGTGCTGAGGACAGT	4542
rs747579603	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8540607	CCCAGCTACTCGGGA[C/G]GCTGAGGCAGGAGAA	4542
rs747582661	snp	A/C	1.65578e-05	0.00287726	intron-variant	MYO1F	GRCh38.p7	19:8553459	ATGAATGGAGGAATA[A/C]ATGATCAGTGGTTGG	4542
rs747593139	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8553030	ATTTCCTGCTGGGTT[G/T]TCAATGGACTCTTGT	4542
rs747646232	snp	A/G	1.68542e-05	0.0029029	intron-variant	MYO1F	GRCh38.p7	19:8525432	CTGGCTTAGGCCATG[A/G]GACCCACAACAGACA	4542
rs747646981	snp	C/G	0.000290263	0.0120436	intron-variant	MYO1F	GRCh38.p7	19:8542026	GGACAGTGAGGGACT[C/G]AGAAACCTGGCTGGG	4542
rs747664426	snp	A/G	6.63174e-05	0.00575798	intron-variant	MYO1F	GRCh38.p7	19:8553480	CAGTGGTTGGGGAAG[A/G]GCCCTTTTTAGTGCC	4542
rs747680677	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8564917	AACTGGAATTACAGG[C/T]GCCTGCCACCAAGCC	4542
rs747752153	snp	A/C/T	6.63112e-05	0.00575776	missense, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530228	ACTTGGTGACCGAAT[A/C/T]GGCGAAGTCCACCCG	4542
rs747756979	snp	A/G	4.96866e-05	0.00498406	intron-variant	MYO1F	GRCh38.p7	19:8548233	TGGAGGCAGGGGGCC[A/G]TACCTGGAAGATCTC	4542
rs747807146	snp	A/G	2.03996e-05	0.00319365	missense	MYO1F	GRCh38.p7	19:8522743	ACGGAGGGCCCCGGG[A/G]AGGCCTGTGGGTGCC	4542
rs747841125	snp	C/T	6.69053e-05	0.00578344	missense, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8541928	TGGTCTGCATCAGCT[C/T]TATGAGGTCGGAGAA	4542
rs747851169	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8569353	GTGGGTGGGGTAGGA[A/C]GGACGGGTAGCTTCT	4542
rs747866245	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8554415	CAAACCTCCCTGGGG[G/T]TGGTGATGTTTCAGC	4542
rs747887659	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8556750	AAATTAGCCAGGTGT[C/G]CTGGCACATGCCTGT	4542
rs747891922	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8547930	CAGAGAGGTGGGAAC[A/G]CGGTGGGGAGGGCTG	4542
rs747892626	snp	A/C	4.41423e-05	0.00469779	intron-variant	MYO1F	GRCh38.p7	19:8536680	TGCTGGAGGTGGGGG[A/C]CCTGGGGGGATCTGG	4542
rs747919322	snp	A/C/T	1.97206e-05	0.00314005	intron-variant	MYO1F	GRCh38.p7	19:8527525	ATGCCTGTAGCCTGG[A/C/T]CAGCCTGGCCACAGA	4542
rs747929333	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8576822	GGCAGAACCCACAGA[C/T]CTTGAGAATGTTGCA	4542
rs748076809	in-del	-/G	1.67959e-05	0.00289787	intron-variant	MYO1F	GRCh38.p7	19:8555799	GCTCCTTGCTGCCCT[-/G]GGGGGTGAGAGGGGG	4542
rs748085282	snp	C/T	2.36706e-05	0.00344017	intron-variant	MYO1F	GRCh38.p7	19:8544508	CTCAGTTTGGTCTGC[C/T]TTGCCTCCCCACAGC	4542
rs748095630	snp	C/T	1.65701e-05	0.00287833	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554716	GCTTGAAGGGGTTTA[C/T]AGAGATGAGCACAGA	4542
rs748113084	snp	A/G	1.73483e-05	0.00294514	intron-variant	MYO1F	GRCh38.p7	19:8521647	CCCCTAGCTGGCCCT[A/G]GAGAAAGCTCTCATG	4542
rs748134909	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8564102	GAAGTGGGTGCTGGC[C/G]GGGCATGGCGGCTCA	4542
rs748163405	snp	C/T	3.32712e-05	0.00407854	intron-variant	MYO1F	GRCh38.p7	19:8555586	CCCTCTGCTCCTTCA[C/T]CCTCCTCTCCGTCCA	4542
rs748169756	snp	A/T	3.81556e-05	0.00436765	intron-variant, synonymous-codon, utr-variant-3-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536625	GTAGGCTGAGTCCCC[A/T]CGGGGTGGGGAGTCA	4542
rs748189585	snp	A/G	0.000100226	0.00707833	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550235	GGCTGCCTGCTCCAC[A/G]TTGAGGGTCACATTG	4542
rs748202146	snp	G/T			intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530043	GGATCTATGCCTGTG[G/T]GCAGGTGCATATGGG	4542
rs748272023	snp	A/G	4.9552e-05	0.0049773	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8553181	AGTCTTGGCGTTGCC[A/G]AAGGCCTCGAGCAGC	4542
rs748281332	snp	C/G	1.78688e-05	0.00298899	intron-variant	MYO1F	GRCh38.p7	19:8547987	CTCATGGTCCTTCCA[C/G]CCCACCCCCACCCCA	4542
rs748331597	snp	C/T	3.49871e-05	0.00418238	synonymous-codon, missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8537020	GTAGTGGGGTGTGCA[C/T]CTCATCAGTGTGGCC	4542
rs748335463	snp	A/C/G			intron-variant	MYO1F	GRCh38.p7	19:8546866	ATATTTTTAGTAGAG[A/C/G]TGGGGTTTCACCATG	4542
rs748340270	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8546580	GTCCAGGCTGGCTTT[C/G]AACCCCCAGGCTCAA	4542
rs748371321	snp	C/T	1.68315e-05	0.00290094	intron-variant	MYO1F	GRCh38.p7	19:8539902	AGGTAGGGTGGAACT[C/T]AGCCCTCTGCAGGCC	4542
rs748398133	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8530805	AGCACTTCGGGAGGC[C/T]GAGGCGGGTGGATCA	4542
rs748437990	snp	A/G/T	0.000240124	0.0109549	intron-variant	MYO1F	GRCh38.p7	19:8555825	GGGGGGTCGGGGTGA[A/G/T]CCCTTGCACGGGGAT	4542
rs748440386	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8562500	TTTTGTTCAGTGTGC[C/T]AAGAGCTCAACACTT	4542
rs748504626	in-del	-/G			intron-variant	MYO1F	GRCh38.p7	19:8534365	AGGCTGGAGTGCAGT[-/G]GGCGCAATCTCAGCT	4542
rs748515052	snp	C/T	1.66685e-05	0.00288686	missense	MYO1F	GRCh38.p7	19:8522422	CGTTGAAGCTCAGCT[C/T]GTCCACATCTTGGCC	4542
rs748537608	snp	C/T	6.62405e-05	0.00575464	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8551770	GTCGCTTCTGTCGTC[C/T]GTGCCGTCCACCTGG	4542
rs748538088	snp	A/C	1.67697e-05	0.00289561	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8526898	GGAAGCTGTCGGCGG[A/C]ATCCTCTTGGAGGAT	4542
rs748591477	snp	A/G	1.67371e-05	0.0028928	synonymous-codon, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536312	CTGGTCGGGCTCCAT[A/G]TTGACCGCCCGAAGC	4542
rs748612340	snp	G/T	0.000284235	0.0119179	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526773	CGAGATGGTGCTGGG[G/T]TTGGCGGGGCCGTAC	4542
rs748657605	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8550836	TTCAGTCACTTGCCG[C/T]GTGACCTTGGGTAAG	4542
rs748702962	snp	G/T	1.65701e-05	0.00287833	intron-variant	MYO1F	GRCh38.p7	19:8551694	AGGAGGGTTTCTGGG[G/T]CTGAGGTCTGCCTGG	4542
rs748753748	snp	A/G	1.65638e-05	0.00287778	intron-variant	MYO1F	GRCh38.p7	19:8554602	AGGTCTCAGCCCAGG[A/G]CTGGGGGCCAGGAGT	4542
rs748836525	snp	A/G	0.000198784	0.00996757	intron-variant	MYO1F	GRCh38.p7	19:8551712	GAGGTCTGCCTGGCC[A/G]GGGACTGGAGTAGAG	4542
rs748948837	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8552858	GGGAATAAATTGGAC[C/G]TGAAATGTGAATGGG	4542
rs748952009	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8573204	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	4542
rs748962074	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8552197	ATGTCAGCACCCCAG[C/T]GTCCTGGGGTGCAGG	4542
rs749020389	snp	A/G	1.68491e-05	0.00290245	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544304	GGGCGCACCTTGCCA[A/G]CGTAGTGGTGGATGA	4542
rs749028387	snp	A/C/T	8.27978e-05	0.00643373	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554518	GTCGATAAGCATGTT[A/C/T]CGGTACATGTTGTCC	4542
rs749036149	in-del	-/C	3.39495e-05	0.0041199	intron-variant	MYO1F	GRCh38.p7	19:8548007	CCCCCACCCCAGGAT[-/C]CCCCATCCCTGACTG	4542
rs749094813	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8539189	GGAGGCTGAGGCAGG[C/T]GGATCACCTGAGGTC	4542
rs749201759	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8547708	AATCCTTGCCTCAGG[C/T]TCTGCTTCTGGGGGA	4542
rs749205031	snp	A/G	1.68835e-05	0.00290542	synonymous-codon, stop-gained, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536993	GGTCTCGTTGGGTTT[A/G]ATGCAGCGGATGTAG	4542
rs749214222	snp	A/G	8.28192e-05	0.00643449	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555688	CCATGAAGCGCTTCC[A/G]GAGGTTGGCGGCAAT	4542
rs749250448	in-del	-/CTCTCTCT			intron-variant	MYO1F	GRCh38.p7	19:8553894	ACACACACACACACA[-/CTCTCTCT]CTCTCTCTCTCTCTC	4542
rs749302245	in-del	-/CAAA	0.00166433	0.0287992	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8536238	TCTCTGCCTGTCCCT[-/CAAA]CAAACACACTCACCG	4542
rs749323853	snp	A/C	2.16219e-05	0.00328793	intron-variant	MYO1F	GRCh38.p7	19:8525606	GACAGACAGACCACG[A/C]TCTTTGCCCCGCCCA	4542
rs749333226	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8539039	GCCTGTAATCCCAGC[A/G]CTTTGGGAGGCTGAG	4542
rs749358150	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8528997	TTAAGGTGATGGTAT[A/G]CAGGTCACCTGAGAG	4542
rs749384991	snp	C/T	4.97616e-05	0.00498782	intron-variant	MYO1F	GRCh38.p7	19:8550522	CGCAGTTCACCCACC[C/T]ACAGGCCTCCATCCA	4542
rs749484151	snp	C/T	0.000116292	0.00762445	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8530495	ACTTCCGGACAGCCA[C/T]GTGGCGCCGCCAGGC	4542
rs749527668	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8539566	GTGCCACTGCACTCC[A/G]TCCTGGGTGACAGAG	4542
rs749532848	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8528917	GTGAATGTGCAAGCC[A/G]GTTGAGCTGGCCTGC	4542
rs749581146	snp	C/T	1.6519e-05	0.00287388	intron-variant	MYO1F	GRCh38.p7	19:8553301	GTGGGGCTGCACTAC[C/T]ATGCAGGTGAGGGCG	4542
rs749619456	in-del	-/GAGAA			intron-variant	MYO1F	GRCh38.p7	19:8565234	GACCAGATGGTTGAT[-/GAGAA]GAGACAATAAAAATT	4542
rs749625311	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8532730	GTCTCTACAAAAACT[A/G]AGCAAAAATTAGCTG	4542
rs749657585	snp	C/T	1.65669e-05	0.00287805	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8548086	GCTGCAGCTTCTCAT[C/T]GACGAAGTTGATGCA	4542
rs749693398	snp	A/G	1.72865e-05	0.00293989	intron-variant	MYO1F	GRCh38.p7	19:8555831	TCGGGGTGAGCCCTT[A/G]CACGGGGATGCGGCA	4542
rs749709330	snp	A/G/T	3.31209e-05	0.00406935	missense, synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8551776	TCTGTCGTCCGTGCC[A/G/T]TCCACCTGGTAGGTG	4542
rs749746701	snp	A/G	1.67621e-05	0.00289495	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8526911	GGCATCCTCTTGGAG[A/G]ATGAAGAAGTCGTCC	4542
rs749762149	snp	C/T	1.74278e-05	0.00295188	missense	MYO1F	GRCh38.p7	19:8522490	GTCCGAGGCTGGGGC[C/T]TGGGTCGGCCCACAC	4542
rs749791892	snp	C/T			utr-variant-3-prime, downstream-variant-500B	MYO1F	GRCh38.p7	19:8521002	CTTGGGTCAGTGAAC[C/T]TCTCTGAACCTCCAT	4542
rs749818683	snp	G/T	3.35993e-05	0.0040986	intron-variant	MYO1F	GRCh38.p7	19:8555799	GCTCCTTGCTGCCCT[G/T]GGGGGTGAGAGGGGG	4542
rs749854928	snp	C/G	7.00636e-05	0.00591835	intron-variant	MYO1F	GRCh38.p7	19:8547990	ATGGTCCTTCCACCC[C/G]ACCCCCACCCCAGGA	4542
rs749867467	snp	C/G	3.3614e-05	0.0040995	missense, utr-variant-3-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536584	GGCCCAGGTATTCCA[C/G]CTGGTGCTTGACTCT	4542
rs749867489	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8527995	TTGGGAGGCCGAGGC[A/G]GGCAGATCATGAGGT	4542
rs749917294	snp	C/T	2.1712e-05	0.00329477	intron-variant	MYO1F	GRCh38.p7	19:8544490	AGCGGGAGCCAGCAG[C/T]GGCTCAGTTTGGTCT	4542
rs749937426	in-del	-/G	1.65201e-05	0.00287398	intron-variant	MYO1F	GRCh38.p7	19:8553272	AGTCAGACTGAGGCA[-/G]GGAGTGCAGATGGGT	4542
rs749944917	snp	C/T	1.66846e-05	0.00288826	intron-variant	MYO1F	GRCh38.p7	19:8554774	GGGTCGTGTGGTGTC[C/T]TGGTAGGTTTTGTCC	4542
rs750003470	snp	A/G	5.29339e-05	0.00514433	intron-variant	MYO1F	GRCh38.p7	19:8536655	ACCAGTCCTGGGGGT[A/G]GGTGGGAGGTGCTGG	4542
rs750015683	snp	C/T	1.66441e-05	0.00288474	intron-variant	MYO1F	GRCh38.p7	19:8522356	CTCCCCTCACCCCAG[C/T]TTCTGCCCTGGTACA	4542
rs750031021	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8548754	TACAAGGGCCTGCCA[C/G]CACGCCCGGCTAATT	4542
rs750034709	in-del	-/CTCT/CTCTCT			intron-variant	MYO1F	GRCh38.p7	19:8553890	ACACACACACACACA[-/CTCT/CTCTCT]CACACTCTCTCTCTC	4542
rs750078685	in-del	-/TC			intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526351	CAAAACTCAAAAGTC[-/TC]TCTCTCTCTCTCTCT	4542
rs750084762	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8535954	CCAAAGTGCTGGGAT[G/T]ACAGGCATGAGCCAC	4542
rs750119331	snp	C/G	1.79864e-05	0.00299881	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544438	GGCGCACACGTCGTC[C/G]AAGACGCTCATGATG	4542
rs750193161	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8551474	TTCCTGCCTCTGCCT[C/T]CCCAGTAGCTGGGAT	4542
rs750216158	snp	A/G/T	0.000231277	0.0107512	intron-variant	MYO1F	GRCh38.p7	19:8553248	GGCAGAGGCAGGTGG[A/G/T]GTGGGAAGAAGTCAG	4542
rs750275283	snp	G/T	1.89166e-05	0.00307538	intron-variant	MYO1F	GRCh38.p7	19:8525582	AAGAAGAGTGTCAGG[G/T]AGTTGAATGACAGAC	4542
rs750300644	snp	A/G	1.66418e-05	0.00288455	intron-variant	MYO1F	GRCh38.p7	19:8537088	ACGGGTGGGTGGGGG[A/G]CACAGAGATGGGACC	4542
rs750306619	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8557853	AGGCCAGTCCCTGAC[G/T]TCTCTGTGGCATTTG	4542
rs750324875	snp	C/G	1.65778e-05	0.002879	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530446	CCCGCGCCGTTTACC[C/G]GAAGCCTCTCACCTT	4542
rs750365581	snp	C/T	1.65214e-05	0.0028741	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8553169	GTTGTTGCGCACAGT[C/T]TTGGCGTTGCCGAAG	4542
rs750405338	snp	A/C/G	3.90436e-05	0.00441821	intron-variant	MYO1F	GRCh38.p7	19:8522623	TGGAGCTGCCCTCCC[A/C/G]CCCCACCTACCCGGC	4542
rs750490893	snp	A/G			splice-donor-variant	MYO1F	GRCh38.p7	19:8553348	TGTTTTCCTCGTCTC[A/G]CCTGGACCTTCTCGC	4542
rs750553132	snp	C/T	0.000117745	0.00767194	missense, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8541982	AGAAGCCGCTGACGT[C/T]GTAGGAGACCTGGAG	4542
rs750573351	snp	A/G	1.68029e-05	0.00289848	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8526872	AAACTCGGTCTTGAA[A/G]ACGCTCTCCAGGAAG	4542
rs750578211	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8521906	GTGATCCTCCTGCCT[C/T]AGCCACTGAAAGTGC	4542
rs750640804	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8562967	GGGCCTTCTTGGACC[A/G]CTGACCTTAGCACCT	4542
rs750694674	snp	C/T	1.65641e-05	0.00287781	intron-variant	MYO1F	GRCh38.p7	19:8554457	CAGCAGGGTCTGTGG[C/T]CCCCCAACTCTGTCC	4542
rs750703902	snp	G/T	3.35076e-05	0.004093	synonymous-codon, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536279	CTTGACAAAGACCTT[G/T]GTGCTCCCCATCTGG	4542
rs750713662	snp	A/T			intron-variant	MYO1F	GRCh38.p7	19:8554331	GTGAGTCAGATGGTG[A/T]CAAGGAAAATAAAAC	4542
rs750731175	snp	C/G	1.90801e-05	0.00308864	missense	MYO1F	GRCh38.p7	19:8522733	AGGGATGTGGACGGA[C/G]GGCCCCGGGGAGGCC	4542
rs750807289	in-del	-/GAA	1.67624e-05	0.00289498	cds-indel, nc-transcript-variant	MYO1F	GRCh38.p7	19:8526914	ATCCTCTTGGAGGAT[-/GAA]GAAGTCGTCCTGTCG	4542
rs750930029	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8545497	ATGAGGGGCGGAAGG[C/G]ACATTTTGGTTGTTA	4542
rs750952250	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8555261	TATAATCCCAGCTAC[C/T]TGGGAGGCTGAGGCA	4542
rs750974944	snp	A/G	9.95058e-05	0.00705287	synonymous-codon, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530205	CCTCACCTTGAAGCG[A/G]CGGTCGTACTTGGTG	4542
rs750986710	snp	A/C	8.28e-05	0.00643375	intron-variant	MYO1F	GRCh38.p7	19:8548170	TGTCCTGGTGCTGGA[A/C]GTTCTTGTGGCCACC	4542
rs751055787	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8568239	CTATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT	4542
rs751056439	snp	G/T	1.65608e-05	0.00287752	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8552074	CATTTTCATTTTGCA[G/T]GACCACGCGGGACTT	4542
rs751067455	snp	A/G	1.65682e-05	0.00287817	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555728	GGTGATCTGGGGAAG[A/G]AGCACCATGTCATCC	4542
rs751110493	in-del	-/G	5.02871e-05	0.00501408	intron-variant	MYO1F	GRCh38.p7	19:8541863	TCCCTCCATCCCCTT[-/G]GGGGGGTTGTAGCCG	4542
rs751143648	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8558537	TCTCCTCTTCCAGGA[A/G]GCCTGCCCTGGTTGC	4542
rs751196739	snp	A/G	1.65608e-05	0.00287752	intron-variant	MYO1F	GRCh38.p7	19:8545637	CCCCCGCCAAAGTTG[A/G]CCCAGCCCTCACCAG	4542
rs751212776	snp	C/T	1.65647e-05	0.00287786	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555669	GGTACGAAGATGTAG[C/T]CGTCCATGAAGCGCT	4542
rs751231670	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8546344	GCTGGGATTACAGGC[A/C]TGAGCCACCGCACAC	4542
rs751232220	snp	A/G	1.66371e-05	0.00288414	synonymous-codon	MYO1F	GRCh38.p7	19:8522384	ACACACACCTTCCAT[A/G]AGGATCTCAATGACC	4542
rs751282959	snp	G/T	4.21363e-05	0.00458981	intron-variant	MYO1F	GRCh38.p7	19:8536666	GGGTGGGTGGGAGGT[G/T]CTGGAGGTGGGGGAC	4542
rs751316838	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8549862	CTGGAGTACAATAGC[A/G]CAATCATAGCTCACT	4542
rs751322202	in-del	-/T			intron-variant	MYO1F	GRCh38.p7	19:8564769	AGCCCGTGTTTCCTG[-/T]TTTTTTTTTTGTTGT	4542
rs751355344	snp	A/G	1.68148e-05	0.0028995	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8536246	CTGTCCCTCAAACAC[A/G]CTCACCGACTCTGGG	4542
rs751357754	snp	C/T	9.94052e-05	0.00704931	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550592	CTCGGGCGTAATTCC[C/T]GTCTTCACAGAAACT	4542
rs751391836	snp	A/C/G	1.71749e-05	0.00293038	intron-variant	MYO1F	GRCh38.p7	19:8521638	CTTGAGGTGCCCCTA[A/C/G]CTGGCCCTGGAGAAA	4542
rs751395908	snp	C/T	3.92534e-05	0.00443003	missense, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526579	CACCGCCCCAGCCCT[C/T]CTTCTTCACCCGAAA	4542
rs751398791	snp	A/G	1.84759e-05	0.00303935	intron-variant	MYO1F	GRCh38.p7	19:8540079	TGGCTAGACTTTCGG[A/G]TACTCTTCCTCCAGG	4542
rs751437680	snp	C/G/T			intron-variant	MYO1F	GRCh38.p7	19:8539370	GGTGAGCCGAGATCA[C/G/T]GCCATTGCACTCCAG	4542
rs751466630	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8550470	CACATTTTTTTCCTC[A/G]TGGGCTTTCAGCTTC	4542
rs751499000	snp	C/T	2.90381e-05	0.00381028	intron-variant	MYO1F	GRCh38.p7	19:8550401	GGACAGTTGGTTGGG[C/T]TCTTGTGCCTCCTGC	4542
rs751538870	snp	A/G	1.65326e-05	0.00287507	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8553362	CACCTGGACCTTCTC[A/G]CCTCCGCCAGACACC	4542
rs751671950	snp	C/G/T	6.68789e-05	0.00578235	intron-variant	MYO1F	GRCh38.p7	19:8527314	GTGAGAGTGACTGTG[C/G/T]GGCAGGTAAGGACCT	4542
rs751725183	snp	A/G	3.75559e-05	0.00433319	missense	MYO1F	GRCh38.p7	19:8522533	GTTGCCCCACGCTGC[A/G]CTTCCTCTGCATGCT	4542
rs751742910	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8532455	AAATACTGTAAATCT[A/G]TAGTAATAAAAACAA	4542
rs751748703	snp	C/T	1.68562e-05	0.00290307	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544329	GGATGACGAAGCCGG[C/T]GCTCCAGCTGTTGAA	4542
rs751808278	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8564758	TGGGGTCAGGGGAGC[C/T]CGTGTTTCCTGTTTT	4542
rs751812345	snp	C/G	3.35999e-05	0.00409864	missense	MYO1F	GRCh38.p7	19:8525502	GGCGCAGGGGCCGCC[C/G]GGGTAGGGGCTTGGG	4542
rs751842442	snp	C/G	1.67419e-05	0.00289321	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8536436	GGAGTGCTCATAGCA[C/G]ACAGGCCTGGCTGGG	4542
rs751856878	snp	A/C	3.31225e-05	0.00406941	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8551750	CTCACCAGAGTCTCA[A/C]CAAAGTCGCTTCTGT	4542
rs751868286	snp	A/G	3.38015e-05	0.00411091	intron-variant	MYO1F	GRCh38.p7	19:8544278	GAGGCACAGGGTAGG[A/G]TAGGGGCAGGGGGCG	4542
rs751936125	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8573124	CCATCCTTGCTAACA[C/T]GGTGAAACCCCATCT	4542
rs751995103	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8554084	CCTCCTCAGCCTCTT[C/G]AGTAGCTGGGGACTA	4542
rs751995402	snp	C/T	1.66632e-05	0.0028864	intron-variant	MYO1F	GRCh38.p7	19:8552193	AACCATGTCAGCACC[C/T]CAGTGTCCTGGGGTG	4542
rs752032414	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8554011	GCCCAGGCTGGAGTG[C/T]AGTGGTGTGATCATA	4542
rs752081548	snp	A/C	1.69602e-05	0.00291201	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550163	AGCCCCACTCGCCTC[A/C]ACGAGGAAGTCGAAG	4542
rs752136118	snp	A/G	1.81599e-05	0.00301324	intron-variant	MYO1F	GRCh38.p7	19:8522846	TGTGGCAGGAGCAAG[A/G]ATGAAGACATGTATT	4542
rs752137230	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8525827	AGGGTTGCCGCTCTG[G/T]CCGCACCCCTCTACA	4542
rs752186562	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8567194	GCCTCATCCTCTCGA[A/G]TAGCTGGGATTATAG	4542
rs752222082	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8560665	CTGCAGCCTTGACCT[C/T]CTGGGCTCAAGTGAT	4542
rs752235811	snp	C/T	1.65605e-05	0.0028775	missense, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8545723	CAGCGGATGCCTTCC[C/T]GCACATACTCCTCCT	4542
rs752241536	snp	C/T	1.65704e-05	0.00287836	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530408	GCTCCTGATACAGCT[C/T]CTCCAGGTCCTTGTG	4542
rs752286942	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8529415	CACGTAGGTTCAGGG[C/G]TGTCTGGGGCAGAAG	4542
rs752334138	snp	A/G	0.00015035	0.00866904	intron-variant	MYO1F	GRCh38.p7	19:8552206	CCCCAGTGTCCTGGG[A/G]TGCAGGTGGGGGAAG	4542
rs752338663	snp	C/T	1.67567e-05	0.00289449	synonymous-codon, missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536975	CCAGTCTCGGGGCCT[C/T]TTGGTCTCGTTGGGT	4542
rs752355623	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8539251	GAAACCCTGTCTCTA[A/C]TGAAAATACAAAATT	4542
rs752401021	snp	C/G	3.3134e-05	0.00407012	missense, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530271	CAGGAACTGACGCAG[C/G]TCGGGCCGCTCCTCC	4542
rs752406124	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8528261	AGATCAGGCGCGGTG[G/T]CACACGCCTGTAATC	4542
rs752433479	snp	A/G	1.66382e-05	0.00288424	synonymous-codon	MYO1F	GRCh38.p7	19:8522396	CATGAGGATCTCAAT[A/G]ACCTCGTTCACGTTG	4542
rs752451929	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8568069	CTGACCATTCTCTCC[C/T]TCTCTATCCTGCCCC	4542
rs752532993	snp	C/T	6.62394e-05	0.00575459	intron-variant	MYO1F	GRCh38.p7	19:8545644	CAAAGTTGACCCAGC[C/T]CTCACCAGCTTGTTT	4542
rs752555964	snp	A/G	1.69037e-05	0.00290716	missense	MYO1F	GRCh38.p7	19:8522458	ACTGGTATAGGGCCC[A/G]GCACCTGGGACCATG	4542
rs752576804	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8532097	CACTCCAGCCTGGGC[A/G]ACAGAGTGAGACTCA	4542
rs752592442	snp	C/T	3.31367e-05	0.00407029	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550617	GAAACTGATGTTCCC[C/T]AGGTGCAAGATCCCC	4542
rs752609847	snp	A/T	1.68929e-05	0.00290623	missense, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526596	TTCTTCACCCGAAAC[A/T]GTAGTCTATGGGGAG	4542
rs752683685	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8552660	ACCATTTTATGGATG[A/G]GCAAACAGAGGAAAC	4542
rs752765289	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8525376	CCTGGACAGAGAAGT[G/T]AGTGGTAAACTGTGT	4542
rs752820866	snp	C/T	1.67843e-05	0.00289687	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8539988	GGCGCCCCTTCTTGT[C/T]TCCATCCAGCTTCTC	4542
rs752824167	snp	C/T	1.65605e-05	0.0028775	intron-variant	MYO1F	GRCh38.p7	19:8548155	GGGTCCTTCCCTCAA[C/T]GTCCTGGTGCTGGAA	4542
rs752838514	in-del	-/A			intron-variant	MYO1F	GRCh38.p7	19:8566481	TGGTCTATGCTTTTT[-/A]AAAAAAAATTTTATT	4542
rs752863496	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8541654	GGCTGGTCTCAAACT[C/G]TTGGCCTCAAGAGAT	4542
rs752892354	snp	C/T	1.90776e-05	0.00308844	missense	MYO1F	GRCh38.p7	19:8522543	GCTGCGCTTCCTCTG[C/T]ATGCTGTGGGCACAG	4542
rs752941186	snp	C/G	1.87887e-05	0.00306496	utr-variant-3-prime	MYO1F	GRCh38.p7	19:8521517	GAGAAGGCAGTATCC[C/G]AGGGCCCAGCTCAGA	4542
rs752951007	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8531489	GAGTAGCTGGGACTA[C/G]AGCTGTGAGCCACCA	4542
rs752994826	snp	C/T	1.68391e-05	0.0029016	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8527433	CTTCACTTTCTCTCG[C/T]CCAATCACATACACA	4542
rs753018608	snp	A/G	1.65641e-05	0.00287781	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554657	CCCCAGCCTCACCGC[A/G]CCCTGATAGAGGTCG	4542
rs753049755	snp	G/T	1.66913e-05	0.00288883	intron-variant	MYO1F	GRCh38.p7	19:8527320	GTGACTGTGCGGCAG[G/T]TAAGGACCTGGCTTC	4542
rs753113522	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8527896	GGGATTACAGGTGTG[C/T]GCCACCACGCCTGGC	4542
rs753135343	snp	C/T	0.00011608	0.0076175	intron-variant	MYO1F	GRCh38.p7	19:8551985	TCCCATTGTCCACCC[C/T]GCTGGGCTCCAGGTG	4542
rs753140274	snp	C/T	1.68496e-05	0.0029025	splice-donor-variant	MYO1F	GRCh38.p7	19:8544296	GGGGCAGGGGGCGCA[C/T]CTTGCCAGCGTAGTG	4542
rs753190470	in-del	-/TC			intron-variant	MYO1F	GRCh38.p7	19:8561515	CTTCTCTCTCATTCT[-/TC]TCTCTTTCTCTCTTC	4542
rs753190472	in-del	-/G	1.65463e-05	0.00287626	intron-variant	MYO1F	GRCh38.p7	19:8553099	TAGAAAGGTCAGCAC[-/G]GAGGGAGCAGCTGCT	4542
rs753226203	snp	C/T	3.38484e-05	0.00411376	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544350	AGCTGTTGAAATGCT[C/T]GTGGGTCCCCACAGC	4542
rs753233424	snp	A/G	5.54319e-05	0.0052643	intron-variant	MYO1F	GRCh38.p7	19:8525574	GGCTCTGAAAGAAGA[A/G]TGTCAGGGAGTTGAA	4542
rs753243963	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8523766	CTCATGATATTCTCC[C/T]CTCTCAGCCTCCTAA	4542
rs753258822	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8563455	GGCGTGCACCACCAC[A/G]CCCAGCTAACGTTTT	4542
rs753284693	snp	C/T	6.78979e-05	0.00582618	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544357	GAAATGCTCGTGGGT[C/T]CCCACAGCCGCCTGC	4542
rs753313833	snp	A/C	1.65625e-05	0.00287766	intron-variant	MYO1F	GRCh38.p7	19:8554586	CCTGGCAGGGGAGGT[A/C]AGGTCTCAGCCCAGG	4542
rs753409156	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8566864	GTTTACAAACAGAGA[G/T]AGAGTCTCGCTATGT	4542
rs753465471	snp	A/G	7.0342e-05	0.0059301	utr-variant-3-prime	MYO1F	GRCh38.p7	19:8521526	GTATCCCAGGGCCCA[A/G]CTCAGATCTTCTCCA	4542
rs753466592	snp	C/G	4.97566e-05	0.00498757	missense, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530465	GCCTCTCACCTTCCT[C/G]CCGCATCTCCTCGTA	4542
rs753485114	snp	C/T	3.58764e-05	0.0042352	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550308	CTGGTCAGCTTCTCC[C/T]GCAGTCGCCCGCTGT	4542
rs753496911	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8524853	GAGAAGCAGAGAAAA[C/T]GGCCCAAAGGCCTGG	4542
rs753504849	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8549738	TCAAACTCCAGACCT[C/G]AAGTGATCCATCCAC	4542
rs753542644	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8537540	TCCACCACCTGGATC[C/T]AAGAGATCCTTCTGC	4542
rs753548882	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8526938	GTCCTGTCGCGTGCT[A/G]GGGAGGGGCGGGTGA	4542
rs753576044	snp	G/T	3.37149e-05	0.00410564	synonymous-codon	MYO1F	GRCh38.p7	19:8525524	GGGCTTGGGACGACC[G/T]CCGAGGTTTTCCCTT	4542
rs753590244	snp	A/G	1.65168e-05	0.00287369	intron-variant	MYO1F	GRCh38.p7	19:8553239	ACGTGCTGGGGCAGA[A/G]GCAGGTGGAGTGGGA	4542
rs753597352	snp	C/G	2.77373e-05	0.00372396	intron-variant	MYO1F	GRCh38.p7	19:8537083	TGAAGACGGGTGGGT[C/G]GGGGGCACAGAGATG	4542
rs753703619	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8532492	GCCTGTCAGAGAATA[C/G]AATGATTAACTGGAA	4542
rs753716553	snp	C/T	3.31444e-05	0.00407076	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530424	CTCCAGGTCCTTGTG[C/T]CCCCACCCCGCGCCG	4542
rs753721846	in-del	-/G	0.00016562	0.00909851	intron-variant	MYO1F	GRCh38.p7	19:8554605	TCTCAGCCCAGGGCT[-/G]GGGGCCAGGAGTCTG	4542
rs753728250	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8541532	CTCCTGGGTTCAAGA[C/G]ATTCTTATGCTTCCA	4542
rs753730207	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8530589	CTGGGCGGGGGTCGT[G/T]GGGGGCAAGGGTGAG	4542
rs753741653	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8559260	AGCAGAAGTGTCCAC[C/G]TGGGCAACTGTAAGG	4542
rs753745875	snp	A/G	1.70038e-05	0.00291575	missense	MYO1F	GRCh38.p7	19:8522466	AGGGCCCGGCACCTG[A/G]GACCATGTGTCCGAG	4542
rs753786050	in-del	-/AAG			intron-variant	MYO1F	GRCh38.p7	19:8564396	TGAAAACAACAAAAA[-/AAG]AAGGAGGTGCTGACT	4542
rs753830104	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8568881	AGCCAAGATTACGTC[A/G]TTGCACTCCAGCCTG	4542
rs753851477	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8531334	CCTGGGCAACAAGAG[C/G]AAAACTTCATCTCAA	4542
rs753853276	snp	C/G	3.35104e-05	0.00409317	intron-variant	MYO1F	GRCh38.p7	19:8527291	GAATGAGGGCAGCCA[C/G]GGGACAGGTGAGAGT	4542
rs753914209	snp	C/T	1.6768e-05	0.00289546	missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536269	ACTCTGGGTTCTTGA[C/T]AAAGACCTTGGTGCT	4542
rs753929547	snp	C/T	1.65337e-05	0.00287517	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8553391	CCTTGGAGATGTAGC[C/T]CATGATATATTTGGC	4542
rs753937067	snp	A/G	1.67832e-05	0.00289677	synonymous-codon, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8541965	GTCTCGGTTCCTCTC[A/G]CAGAAGCCGCTGACG	4542
rs753946001	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8549006	CCAGGCTGGAATGCC[A/G]GTGGCGCAATCTCGG	4542
rs753946970	snp	C/T	6.91384e-05	0.00587915	intron-variant	MYO1F	GRCh38.p7	19:8530586	AAGCTGGGCGGGGGT[C/T]GTGGGGGGCAAGGGT	4542
rs753971231	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8571346	TGTGCAAACAACATT[C/T]TCACCTCCAAAGGCT	4542
rs754084123	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8552482	ATGTTGGCCAGGCTG[A/G]TCTTGAACTCCAGAC	4542
rs754112921	snp	C/T	1.80068e-05	0.00300051	synonymous-codon	MYO1F	GRCh38.p7	19:8522723	GCTGGCTCCCAGGGA[C/T]GTGGACGGAGGGCCC	4542
rs754113655	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8545518	TTGGTTGTTATCTGT[C/T]GCTGGAAGTCCTGAG	4542
rs754129586	snp	C/T	1.67981e-05	0.00289806	intron-variant, missense, stop-gained, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536642	GGGGTGGGGAGTCAC[C/T]AGTCCTGGGGGTGGG	4542
rs754132433	snp	A/G	1.65641e-05	0.00287781	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8548274	ATGTCCAGCACACCG[A/G]TGCTGTACTCTTCCT	4542
rs754136267	snp	A/G/T	8.37828e-05	0.00647188	intron-variant	MYO1F	GRCh38.p7	19:8541865	CCCTCCATCCCCTTG[A/G/T]GGGGTTGTAGCCGGA	4542
rs754142078	snp	C/T	1.65861e-05	0.00287972	intron-variant	MYO1F	GRCh38.p7	19:8551967	CCCCCTAGGTGTTTA[C/T]CTTCCCATTGTCCAC	4542
rs754181025	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8560300	CCATCCTGGCTAACA[C/T]GGTGAAACCCCATCT	4542
rs754189832	snp	C/G	1.69836e-05	0.00291402	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8527454	CACATACACACACTT[C/G]GGCGTCAGGATCAAG	4542
rs754201930	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8557576	CAAAGTGGTGGGATT[A/G]TAGGCGTAAGCTACT	4542
rs754248437	in-del	-/AG			intron-variant	MYO1F	GRCh38.p7	19:8554347	CAAGGAAAATAAAAC[-/AG]AGTGAGGGCAGAGAG	4542
rs754347908	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8562376	GCACTGGTGCGATCA[C/T]ACCTCACTGCGGCCT	4542
rs754368466	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8534851	GGGCTGGTCTTGAAC[C/T]CCTGACCTCGTGATC	4542
rs754372219	snp	C/T	0.000652027	0.0180441	missense, synonymous-codon, utr-variant-3-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536565	ACCCTGATGTTCTCC[C/T]TCAGGCCCAGGTATT	4542
rs754375689	snp	A/G	1.68906e-05	0.00290603	intron-variant	MYO1F	GRCh38.p7	19:8521616	GGATCTGTGGGAGAG[A/G]GGAAAGCTTGAGGTG	4542
rs754392322	in-del	-/T	1.67283e-05	0.00289203	intron-variant	MYO1F	GRCh38.p7	19:8527300	CAGCCAGGGGACAGG[-/T]GAGAGTGACTGTGCG	4542
rs754413199	snp	C/G	4.96915e-05	0.0049843	intron-variant	MYO1F	GRCh38.p7	19:8551903	CATGTTCATGCATCT[C/G]GTGCTTGCCTGGCTC	4542
rs754452234	snp	C/T	1.65608e-05	0.00287752	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8552080	CATTTTGCATGACCA[C/T]GCGGGACTTCTCCAG	4542
rs754469189	snp	A/G	1.67097e-05	0.00289043	intron-variant	MYO1F	GRCh38.p7	19:8552196	CATGTCAGCACCCCA[A/G]TGTCCTGGGGTGCAG	4542
rs754525032	in-del	-/TCCC/TCCCTCCC			intron-variant	MYO1F	GRCh38.p7	19:8561350	GTAGTCAGCATGAAT[-/TCCC/TCCCTCCC]TCCCTCCCTCCCTCC	4542
rs754535521	snp	A/C/G	4.00026e-05	0.00447214	missense	MYO1F	GRCh38.p7	19:8522740	TGGACGGAGGGCCCC[A/C/G]GGGAGGCCTGTGGGT	4542
rs754539457	snp	A/G			intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8536151	TCAGTCTTTCTCTCA[A/G]TCTCTGTCTCCCTCT	4542
rs754582807	snp	A/G	1.6638e-05	0.00288422	missense	MYO1F	GRCh38.p7	19:8522386	ACACACCTTCCATGA[A/G]GATCTCAATGACCTC	4542
rs754622172	in-del	GAGACGGAGTCTTGCTCTGTCGCTCA/TTTTAGCGGGGGTCTCGCTCTTTCCCCCCGGCCGGAG			intron-variant	MYO1F	GRCh38.p7	19:8533373	TTTTTTTTTTTTTTT[lengthTooLong]GGCTGGAGTGCAGTG	4542
rs754629450	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8528063	CCCGTCTCTACTAAA[A/G]ATACAAAAATTAGCT	4542
rs754655882	snp	C/T	1.65647e-05	0.00287786	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555670	GTACGAAGATGTAGT[C/T]GTCCATGAAGCGCTT	4542
rs754657763	snp	A/G	2.21359e-05	0.00332678	intron-variant	MYO1F	GRCh38.p7	19:8536671	GGTGGGAGGTGCTGG[A/G]GGTGGGGGACCTGGG	4542
rs754666016	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8560645	AGTGGCAAGGTCATG[G/T]CTCACTGCAGCCTTG	4542
rs754683729	in-del	-/G	1.65659e-05	0.00287796	intron-variant	MYO1F	GRCh38.p7	19:8555653	CCCAGCCTTGGCCCA[-/G]GGTACGAAGATGTAG	4542
rs754715040	snp	C/T	1.65817e-05	0.00287933	missense, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530216	AGCGGCGGTCGTACT[C/T]GGTGACCGAATCGGC	4542
rs754744275	snp	C/T	7.90045e-05	0.00628459	synonymous-codon, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526586	CCAGCCCTCCTTCTT[C/T]ACCCGAAACTGTAGT	4542
rs754747494	snp	A/G	1.67478e-05	0.00289372	stop-gained, missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536968	TCTCCTCCCAGTCTC[A/G]GGGCCTCTTGGTCTC	4542
rs754747911	snp	A/C	1.83024e-05	0.00302504	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544448	TCGTCCAAGACGCTC[A/C]TGATGCCTGGGGGGC	4542
rs754757548	snp	C/T			missense	MYO1F	GRCh38.p7	19:8525506	CAGGGGCCGCCCGGG[C/T]AGGGGCTTGGGACGA	4542
rs754777569	snp	C/T	1.68255e-05	0.00290043	intron-variant	MYO1F	GRCh38.p7	19:8554788	CCTGGTAGGTTTTGT[C/T]CTCCCTGTCCCCTCA	4542
rs754784576	in-del	-/GAA			intron-variant	MYO1F	GRCh38.p7	19:8527606	GGGAGCCCTCCAGGT[-/GAA]GGTGTATGAGTCGTC	4542
rs754875801	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8548571	TGACTCTGCCCCTGA[A/C]CCTCTCTGCACCTCT	4542
rs754898367	snp	C/T			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578708	AACCACCTGAGGCTC[C/T]TCTTGACATGTGAGG	4542
rs754941160	snp	C/T	2.91617e-05	0.00381838	intron-variant	MYO1F	GRCh38.p7	19:8550404	CAGTTGGTTGGGCTC[C/T]TGTGCCTCCTGCATG	4542
rs754945205	in-del	-/TC			intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8536169	CTGTCTCCCTCTGTC[-/TC]TCTCTCTCTCTCTCT	4542
rs754974610	snp	C/G	1.71811e-05	0.00293091	missense, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526486	CATCGCCCACGCTGA[C/G]CGTGAGGGTCCGACC	4542
rs755015788	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8550750	GCCTCCAACCTGCCT[C/T]CAGGGGCAGGCTTGA	4542
rs755017527	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8551956	CCCTGCCATGCCCCC[C/T]TAGGTGTTTACCTTC	4542
rs755050219	snp	A/T	3.22565e-05	0.00401587	intron-variant	MYO1F	GRCh38.p7	19:8537096	GTGGGGGGCACAGAG[A/T]TGGGACCCTCTGGCC	4542
rs755069858	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8551655	CATGCCTGGCCTGGG[A/C]TTCGGTTTCCTAATT	4542
rs755086346	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8563443	CCTGGGATTATAGGC[A/G]TGCACCACCACGCCC	4542
rs755088166	snp	C/T	4.98973e-05	0.00499461	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8548041	GGCCGCCCACCTGCT[C/T]GGCCTTCAGGGTAAG	4542
rs755109803	snp	A/G	1.6736e-05	0.0028927	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8536450	AGACAGGCCTGGCTG[A/G]GCGTTCTGATGAAGG	4542
rs755136418	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8564803	TTTGAGACAGAGTCT[A/C]GCTCTGTCACCCAGG	4542
rs755210073	snp	C/T	1.65756e-05	0.00287881	intron-variant	MYO1F	GRCh38.p7	19:8545779	GGGCCAGTGAAAAAG[C/T]TGTGGCCACCCTTCC	4542
rs755302659	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8540423	CATTTTAAAATGGTT[A/G]ATAAGGCCGGGTGCG	4542
rs755373455	snp	A/G	0.000124247	0.00788086	intron-variant	MYO1F	GRCh38.p7	19:8522855	AGCAAGGATGAAGAC[A/G]TGTATTAGGGTGATG	4542
rs755378609	snp	A/G	5.03461e-05	0.00501702	missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536359	GGCGTTCGTCCCCAC[A/G]CCACCGCGGCCACGT	4542
rs755390965	snp	C/T	1.66963e-05	0.00288927	intron-variant	MYO1F	GRCh38.p7	19:8550731	AACTGTGCCGTGAAT[C/T]CTGGCCTCCAACCTG	4542
rs755414901	snp	A/G	1.65619e-05	0.00287762	intron-variant	MYO1F	GRCh38.p7	19:8554581	CTGGGCCTGGCAGGG[A/G]AGGTCAGGTCTCAGC	4542
rs755435260	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8524752	GCAGGGGCAAGTTTC[C/T]CTCCTCCTATCCTCT	4542
rs755446835	in-del	-/CCCTTCTCAGGT	1.67105e-05	0.0028905	cds-indel, nc-transcript-variant	MYO1F	GRCh38.p7	19:8527401	ACTTCACACACCTGG[-/CCCTTCTCAGGT]CCCTTCTTCACTTTC	4542
rs755452728	snp	C/T	1.69444e-05	0.00291066	intron-variant	MYO1F	GRCh38.p7	19:8542007	CTGGAGGGGACAGTG[C/T]TGAGGACAGTGAGGG	4542
rs755574416	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8547194	CGGTCCCAGCTACTT[A/G]AGAGGCTGAAGTGGG	4542
rs755593569	snp	A/G	0.000186058	0.00964335	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550175	CTCCACGAGGAAGTC[A/G]AAGAGGCGGGCATAG	4542
rs755613439	snp	C/T	6.89869e-05	0.00587271	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550290	CGGCTGTCCATCTTG[C/T]GGCTGGTCAGCTTCT	4542
rs755626193	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8558609	CCCTGGCTTTCTCAG[C/G]CTCACTCTGTCTCTA	4542
rs755652788	snp	A/C	5.05565e-05	0.0050275	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544297	GGGCAGGGGGCGCAC[A/C]TTGCCAGCGTAGTGG	4542
rs755664368	snp	A/T	6.72484e-05	0.00579825	missense	MYO1F	GRCh38.p7	19:8525514	GCCCGGGTAGGGGCT[A/T]GGGACGACCTCCGAG	4542
rs755742850	snp	G/T	6.63658e-05	0.00576008	intron-variant	MYO1F	GRCh38.p7	19:8537078	AGAAGTGAAGACGGG[G/T]GGGTGGGGGGCACAG	4542
rs755761354	in-del	-/T			intron-variant	MYO1F	GRCh38.p7	19:8562546	TTATTTACTTATTTA[-/T]TTTTTTTGAGGCAGG	4542
rs755770493	snp	A/C/G	4.96984e-05	0.00498469	synonymous-codon, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530274	GAACTGACGCAGCTC[A/C/G]GGCCGCTCCTCCAGC	4542
rs755788001	snp	A/T	1.66682e-05	0.00288684	intron-variant	MYO1F	GRCh38.p7	19:8552210	AGTGTCCTGGGGTGC[A/T]GGTGGGGGAAGGGTT	4542
rs755796289	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8541782	ACACCATCCTGGCCG[C/T]ACAGCCACTCCCCTC	4542
rs755821637	in-del	-/CCCCC	3.84911e-05	0.00438681	intron-variant	MYO1F	GRCh38.p7	19:8547991	GGTCCTTCCACCCCA[-/CCCCC]CCCCCACCCCAGGAT	4542
rs755835273	snp	A/G	1.69086e-05	0.00290758	synonymous-codon	MYO1F	GRCh38.p7	19:8522459	CTGGTATAGGGCCCG[A/G]CACCTGGGACCATGT	4542
rs755846940	in-del	-/C	1.65647e-05	0.00287786	intron-variant	MYO1F	GRCh38.p7	19:8554456	CAGCAGGGTCTGTGG[-/C]CCCCCCAACTCTGTC	4542
rs755862572	snp	A/G	1.65707e-05	0.00287838	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530415	ATACAGCTCCTCCAG[A/G]TCCTTGTGCCCCCAC	4542
rs755866113	snp	A/G	3.35779e-05	0.00409729	synonymous-codon, stop-gained, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536984	GGGCCTCTTGGTCTC[A/G]TTGGGTTTGATGCAG	4542
rs755895884	snp	A/G	3.36791e-05	0.00410346	intron-variant	MYO1F	GRCh38.p7	19:8525451	CCACAACAGACAAGG[A/G]AATATAGCAAGGGAC	4542
rs755932392	snp	A/G	1.65644e-05	0.00287783	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555682	AGTCGTCCATGAAGC[A/G]CTTCCGGAGGTTGGC	4542
rs755973380	in-del	-/AAT			intron-variant	MYO1F	GRCh38.p7	19:8565545	GAAACTCTGTCTCGA[-/AAT]AATAATAATAATAAA	4542
rs756015250	snp	A/G	8.66889e-05	0.00658308	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526604	CCGAAACTGTAGTCT[A/G]TGGGGAGAGAAGAAA	4542
rs756031757	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8557886	CCACTGCTGCCAGGC[C/T]CCTTCCTTCTCCCTC	4542
rs756047959	snp	C/T	4.99825e-05	0.00499888	intron-variant	MYO1F	GRCh38.p7	19:8544513	TTTGGTCTGCCTTGC[C/T]TCCCCACAGCTCGTC	4542
rs756102919	snp	C/T	4.968e-05	0.00498373	intron-variant	MYO1F	GRCh38.p7	19:8545647	AGTTGACCCAGCCCT[C/T]ACCAGCTTGTTTTCG	4542
rs756133274	snp	C/T			utr-variant-3-prime, downstream-variant-500B	MYO1F	GRCh38.p7	19:8520904	TGCTGGGATTACAGG[C/T]GTGAGCCACTGCGCC	4542
rs756136328	snp	C/T	0.000154804	0.00879648	intron-variant	MYO1F	GRCh38.p7	19:8536683	TGGAGGTGGGGGACC[C/T]GGGGGGATCTGGATT	4542
rs756138370	snp	C/G	1.66388e-05	0.00288429	missense	MYO1F	GRCh38.p7	19:8522399	GAGGATCTCAATGAC[C/G]TCGTTCACGTTGAAG	4542
rs756161653	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8561812	AAATCTACCTCCCAG[C/G]TTCAAACGATTCTTC	4542
rs756224380	snp	A/C	1.65438e-05	0.00287605	intron-variant	MYO1F	GRCh38.p7	19:8541858	CGGTCCTCCCTCCAT[A/C]CCCTTGGGGGGTTGT	4542
rs756235757	snp	A/T	1.65184e-05	0.00287384	intron-variant	MYO1F	GRCh38.p7	19:8553299	GGGTGGGGCTGCACT[A/T]CCATGCAGGTGAGGG	4542
rs756248508	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8550080	ATTGGGATTGCAGCC[A/G]TGAGCCACTGCACTC	4542
rs756291793	snp	A/C	3.90625e-05	0.00441924	intron-variant	MYO1F	GRCh38.p7	19:8522555	CTGCATGCTGTGGGC[A/C]CAGGGGGTTTGAGTC	4542
rs756377158	snp	C/T	1.65789e-05	0.0028791	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8548062	TCAGGGTAAGTTCGA[C/T]AAAGATTTGCTGCAG	4542
rs756431782	in-del	-/GGTGAGAGCGTCAGGTGGGACACA	1.67902e-05	0.00289738	intron-variant	MYO1F	GRCh38.p7	19:8526949	TGCTGGGGAGGGGCG[-/GGTGAGAGCGTCAGGTGGGACACA]GGTGAGGGCGACAGG	4542
rs756463006	snp	C/T	6.62405e-05	0.00575464	intron-variant	MYO1F	GRCh38.p7	19:8548157	GTCCTTCCCTCAATG[C/T]CCTGGTGCTGGAAGT	4542
rs756483186	snp	A/G	0.000165593	0.00909775	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8551771	TCGCTTCTGTCGTCC[A/G]TGCCGTCCACCTGGT	4542
rs756496409	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8544799	TATTTATTTAGAGAC[A/G]GAGTCTTGCTCTCTT	4542
rs756522970	snp	G/T	0.00131859	0.0256429	intron-variant	MYO1F	GRCh38.p7	19:8527321	TGACTGTGCGGCAGG[G/T]AAGGACCTGGCTTCA	4542
rs756566288	snp	A/G	1.65627e-05	0.00287769	intron-variant	MYO1F	GRCh38.p7	19:8554587	CTGGCAGGGGAGGTC[A/G]GGTCTCAGCCCAGGG	4542
rs756569428	snp	A/T	3.31235e-05	0.00406948	intron-variant	MYO1F	GRCh38.p7	19:8551895	GGGTGTGCCATGTTC[A/T]TGCATCTGGTGCTTG	4542
rs756591265	snp	A/G	3.38518e-05	0.00411397	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544351	GCTGTTGAAATGCTC[A/G]TGGGTCCCCACAGCC	4542
rs756664731	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8532721	AAAGACCCCGTCTCT[A/G]CAAAAACTAAGCAAA	4542
rs756672035	in-del	-/C	6.63152e-05	0.00575788	intron-variant	MYO1F	GRCh38.p7	19:8545785	GTGAAAAAGTTGTGG[-/C]CACCCTTCCCCCCAT	4542
rs756719190	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8557821	CCTTTCACATCCCCC[A/G]TCCCCTCCCCAGGCC	4542
rs756724343	snp	A/G	1.78957e-05	0.00299124	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544435	GGTGGCGCACACGTC[A/G]TCCAAGACGCTCATG	4542
rs756735265	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8569309	CTCAACCTGCTGGAG[C/T]TCTTGTGAAAGGCAG	4542
rs756766162	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8523545	AAGTAGAGATGGGGT[A/C]TCACTATGTTGCTCA	4542
rs756790942	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8529525	GAGCATGTACCTATG[A/G]ACTAGGCTGCCTGGG	4542
rs756794504	snp	C/T	1.68576e-05	0.00290319	synonymous-codon	MYO1F	GRCh38.p7	19:8525525	GGCTTGGGACGACCT[C/T]CGAGGTTTTCCCTTG	4542
rs756797956	snp	G/T	1.71566e-05	0.00292883	missense	MYO1F	GRCh38.p7	19:8521533	AGGGCCCAGCTCAGA[G/T]CTTCTCCACGTAGTT	4542
rs756813336	snp	A/G	3.31307e-05	0.00406992	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554678	ATAGAGGTCGATCTC[A/G]CGGTCGGTGAAGTAG	4542
rs756871024	snp	C/T	1.65891e-05	0.00287998	missense, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530467	CTCTCACCTTCCTCC[C/T]GCATCTCCTCGTACT	4542
rs756888709	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8575783	CTTGTCTGCCAAGCC[C/G]ACTGTTGACTAAGCA	4542
rs756908880	in-del	-/A			intron-variant	MYO1F	GRCh38.p7	19:8549302	TTGAGACAGGGTCTC[-/A]AGTCTGTTGTCCAGG	4542
rs756936743	in-del	-/CC	1.65754e-05	0.00287879	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530436	TGCCCCCACCCCGCG[-/CC]CCGTTTACCCGAAGC	4542
rs756937114	snp	C/T	0.000724414	0.019018	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550310	GGTCAGCTTCTCCTG[C/T]AGTCGCCCGCTGTCA	4542
rs756939714	snp	C/G	1.69666e-05	0.00291256	intron-variant	MYO1F	GRCh38.p7	19:8555811	CCTGGGGGGTGAGAG[C/G]GGGGTCGGGGTGAGC	4542
rs756991685	snp	C/T	1.70035e-05	0.00291572	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544360	ATGCTCGTGGGTCCC[C/T]ACAGCCGCCTGCAGC	4542
rs757013444	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8549881	TCATAGCTCACTGCA[A/G]CCCCAACCTCCTGGG	4542
rs757027395	snp	C/T	1.65729e-05	0.00287857	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530425	TCCAGGTCCTTGTGC[C/T]CCCACCCCGCGCCGT	4542
rs757136900	snp	A/G	1.65233e-05	0.00287426	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8553164	GAATTGTTGTTGCGC[A/G]CAGTCTTGGCGTTGC	4542
rs757143087	snp	G/T	1.67854e-05	0.00289697	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550198	GGGCATAGAGCCCCT[G/T]GGCCAGGGCATCACG	4542
rs757164846	snp	C/T	1.68821e-05	0.0029053	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536995	TCTCGTTGGGTTTGA[C/T]GCAGCGGATGTAGTG	4542
rs757164936	snp	A/G	1.65693e-05	0.00287826	intron-variant	MYO1F	GRCh38.p7	19:8545760	GAAAAGGGGGTGGAT[A/G]TGGGGGCCAGTGAAA	4542
rs757201118	snp	C/T	1.65875e-05	0.00287984	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555755	ATCCACGCCGCTCTG[C/T]TTCACGTTGTGGCTC	4542
rs757224249	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8564179	TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA	4542
rs757263233	snp	C/T	1.6534e-05	0.00287519	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8553399	ATGTAGCCCATGATA[C/T]ATTTGGCTGCCACTG	4542
rs757307710	snp	A/G	8.84604e-05	0.00664999	missense, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526491	CCCACGCTGACCGTG[A/G]GGGTCCGACCGCCAA	4542
rs757342411	in-del	-/G			intron-variant	MYO1F	GRCh38.p7	19:8523165	GCCTCCCGAGTAGCT[-/G]GGACTACAGGCACCT	4542
rs757350895	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8544639	AAGGCGTTGCAGGGG[C/T]CAGGGATGGAAGGGA	4542
rs757352818	snp	C/T	3.32353e-05	0.00407634	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550628	TCCCCAGGTGCAAGA[C/T]CCCCGCCACGAGCTG	4542
rs757436755	snp	A/G	1.67649e-05	0.0028952	missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536271	TCTGGGTTCTTGACA[A/G]AGACCTTGGTGCTCC	4542
rs757458802	snp	A/G	0.000214761	0.0103602	intron-variant	MYO1F	GRCh38.p7	19:8553311	ACTACCATGCAGGTG[A/G]GGGCGACCCAGCTTA	4542
rs757587528	snp	C/T	1.65858e-05	0.00287969	intron-variant	MYO1F	GRCh38.p7	19:8551971	CTAGGTGTTTACCTT[C/T]CCATTGTCCACCCCG	4542
rs757596507	snp	C/T	1.81424e-05	0.00301179	missense	MYO1F	GRCh38.p7	19:8522639	CCCCACCTACCCGGC[C/T]ATGCCCTGGTCAGGC	4542
rs757598543	snp	C/T	1.65734e-05	0.00287862	splice-donor-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530195	CCCACTAGTGCCTCA[C/T]CTTGAAGCGGCGGTC	4542
rs757617518	snp	C/T	1.68009e-05	0.00289831	missense, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8541973	TCCTCTCGCAGAAGC[C/T]GCTGACGTCGTAGGA	4542
rs757654643	snp	A/G	1.67365e-05	0.00289275	missense, synonymous-codon, utr-variant-3-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536568	CTGATGTTCTCCTTC[A/G]GGCCCAGGTATTCCA	4542
rs757673469	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8537304	GAGCTCTCACGTCTA[C/G]CGCACTCACCACTTA	4542
rs757673536	snp	G/T	1.65605e-05	0.0028775	intron-variant	MYO1F	GRCh38.p7	19:8548163	CCCTCAATGTCCTGG[G/T]GCTGGAAGTTCTTGT	4542
rs757704563	snp	A/C	1.66446e-05	0.00288479	splice-donor-variant	MYO1F	GRCh38.p7	19:8527336	TAAGGACCTGGCTTC[A/C]CCTGAGGGAGACTCC	4542
rs757798944	snp	C/T			missense, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8541984	AAGCCGCTGACGTCG[C/T]AGGAGACCTGGAGGG	4542
rs757810619	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8568980	GGGGTCTCTGAAACA[A/G]GTACAGGAGCGAACA	4542
rs757811033	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8554119	CGTGCACCACCGTGT[C/G]CGGCTAATTATTATC	4542
rs757829604	snp	C/T	0.000136066	0.00824709	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8527457	ATACACACACTTGGG[C/T]GTCAGGATCAAGTCC	4542
rs757833567	snp	C/T	0.000100147	0.00707555	intron-variant	MYO1F	GRCh38.p7	19:8554775	GGTCGTGTGGTGTCC[C/T]GGTAGGTTTTGTCCT	4542
rs757855084	snp	A/G	6.14119e-05	0.00554095	intron-variant	MYO1F	GRCh38.p7	19:8536657	CAGTCCTGGGGGTGG[A/G]TGGGAGGTGCTGGAG	4542
rs757920201	snp	C/T	1.68182e-05	0.00289979	missense	MYO1F	GRCh38.p7	19:8521547	ATCTTCTCCACGTAG[C/T]TTCCTGGGAAAAGGC	4542
rs757921551	snp	C/T	1.65853e-05	0.00287964	intron-variant	MYO1F	GRCh38.p7	19:8551978	TTTACCTTCCCATTG[C/T]CCACCCCGCTGGGCT	4542
rs757976654	snp	A/C	1.73348e-05	0.00294399	synonymous-codon, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526478	GGGCAGCCCATCGCC[A/C]ACGCTGACCGTGAGG	4542
rs758029581	snp	C/G	1.65658e-05	0.00287795	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554687	GATCTCACGGTCGGT[C/G]AAGTAGGGCATCTGC	4542
rs758097575	snp	C/T	0.000217226	0.0104195	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544443	ACACGTCGTCCAAGA[C/T]GCTCATGATGCCTGG	4542
rs758103444	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8529484	CCAAGCATGAATGCA[C/T]GGGTCAGGTGATGTA	4542
rs758106014	snp	C/T			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578335	GTAGAGACGGAATTT[C/T]GCCATGTTGGCCAGG	4542
rs758128599	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8548888	CCACTGCGCCCGGCC[G/T]TGCACCTCTATTTTC	4542
rs758128867	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8559811	AAAAATTAGCTGGGC[A/G]TGGTGGCGCACGCCT	4542
rs758133545	snp	C/T	1.68872e-05	0.00290574	missense, synonymous-codon, utr-variant-3-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536592	TATTCCACCTGGTGC[C/T]TGACTCTGGTGGGGA	4542
rs758209352	snp	C/T	1.903e-05	0.00308458	intron-variant	MYO1F	GRCh38.p7	19:8525585	AAGAGTGTCAGGGAG[C/T]TGAATGACAGACAGA	4542
rs758259822	in-del	-/G			utr-variant-3-prime	MYO1F	GRCh38.p7	19:8521200	TCCCCAACTGTGCCT[-/G]GCACTTTGCCAACAG	4542
rs758337805	snp	C/T	1.67775e-05	0.00289629	synonymous-codon, missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8539977	GGCGGTGCTGGGGCG[C/T]CCCTTCTTGTCTCCA	4542
rs758348210	snp	G/T	1.65198e-05	0.00287395	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8553172	GTTGCGCACAGTCTT[G/T]GCGTTGCCGAAGGCC	4542
rs758367195	snp	G/T	1.65897e-05	0.00288003	missense, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530471	CACCTTCCTCCCGCA[G/T]CTCCTCGTACTTCCG	4542
rs758417688	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8540582	GGGCATGATGGTGGG[C/T]GTCTATAATCCCAGC	4542
rs758532735	snp	C/T	1.65625e-05	0.00287766	intron-variant	MYO1F	GRCh38.p7	19:8551737	GTAGAGGCCGGTGCT[C/T]ACCAGAGTCTCACCA	4542
rs758533761	snp	C/T	1.67978e-05	0.00289804	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8526874	ACTCGGTCTTGAAGA[C/T]GCTCTCCAGGAAGCT	4542
rs758642752	snp	C/T	1.67528e-05	0.00289415	missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536281	TGACAAAGACCTTGG[C/T]GCTCCCCATCTGGTA	4542
rs758730779	snp	A/G	1.67595e-05	0.00289473	synonymous-codon, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536351	GACGCCCTGGCGTTC[A/G]TCCCCACGCCACCGC	4542
rs758734442	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8563566	TGGGCTGGAGTGCAA[G/T]GATGTGATCTCAGCT	4542
rs758763614	snp	C/T	0.000230322	0.0107288	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526622	GGGAGAGAAGAAAGC[C/T]TGGGGGCGCTGGCTG	4542
rs758768612	snp	G/T	3.36208e-05	0.00409991	missense, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530209	ACCTTGAAGCGGCGG[G/T]CGTACTTGGTGACCG	4542
rs758784614	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8523260	GGATGGTCTCGATCT[C/T]CTGACCTTGTGATCC	4542
rs758790784	snp	A/G	3.36457e-05	0.00410143	synonymous-codon, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8541983	GAAGCCGCTGACGTC[A/G]TAGGAGACCTGGAGG	4542
rs758799346	snp	A/G	1.65688e-05	0.00287821	intron-variant	MYO1F	GRCh38.p7	19:8548189	CTTGTGGCCACCCTG[A/G]GCTGCCCCAGGGAGG	4542
rs758850061	snp	C/T	3.30961e-05	0.0040678	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8553424	CCACTGTCTTCCCAG[C/T]TCCACTCTCTCCACT	4542
rs758853315	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8535093	ATTTTTGTACTTTTA[A/G]TAGAGAAGGGGTTTC	4542
rs758855253	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8547031	GACTGGGCATATTAA[C/T]TCATGCCTGTAGTCC	4542
rs758871140	snp	A/G	1.65611e-05	0.00287755	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8552060	GTGGAAGTTCCTCTC[A/G]TTTTCATTTTGCATG	4542
rs758885139	snp	A/G	1.67489e-05	0.00289381	intron-variant	MYO1F	GRCh38.p7	19:8541878	TGGGGGGTTGTAGCC[A/G]GAGGTCCCCATGCCT	4542
rs758904329	snp	C/T	1.65748e-05	0.00287874	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555739	GAAGAAGCACCATGT[C/T]ATCCACGCCGCTCTG	4542
rs758965119	snp	G/T	1.93287e-05	0.00310869	synonymous-codon	MYO1F	GRCh38.p7	19:8522735	GGATGTGGACGGAGG[G/T]CCCCGGGGAGGCCTG	4542
rs758983567	snp	A/T			intron-variant	MYO1F	GRCh38.p7	19:8549744	TCCAGACCTCAAGTG[A/T]TCCATCCACCTCAGC	4542
rs759002472	snp	A/G	1.65787e-05	0.00287907	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8548309	TTTCTGCATAGCACG[A/G]TTGATGGCCTGCGGT	4542
rs759082844	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8539204	CGGATCACCTGAGGT[C/T]GGGAGTTCGAGAATA	4542
rs759092857	snp	C/G	1.65649e-05	0.00287788	intron-variant	MYO1F	GRCh38.p7	19:8551720	CCTGGCCGGGGACTG[C/G]AGTAGAGGCCGGTGC	4542
rs759106961	snp	A/G	1.6842e-05	0.00290184	intron-variant	MYO1F	GRCh38.p7	19:8555801	TCCTTGCTGCCCTGG[A/G]GGGTGAGAGGGGGGT	4542
rs759149469	snp	C/T	1.79219e-05	0.00299344	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8526829	GCCTCCGCGTCGCCT[C/T]CTCGAAGCGCTTGCA	4542
rs759178982	snp	C/T	6.62405e-05	0.00575464	missense, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8545718	GAGTCCAGCGGATGC[C/T]TTCCTGCACATACTC	4542
rs759248390	snp	A/G			missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550264	TGATGGACTCGCTGC[A/G]CCCGCCCCAGCGGCT	4542
rs759295494	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8538490	TTTCACCATGTTGGC[C/T]AGGCTGGTCTTGAAA	4542
rs759305538	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8543286	GCCTGAGAGTGTAGT[C/T]CTGTCTTTTGGGGAG	4542
rs759344792	snp	A/C	3.61513e-05	0.00425139	missense	MYO1F	GRCh38.p7	19:8522791	CCAGGGGCAGGGGGC[A/C]CCCTCTGGCAGAGGG	4542
rs759362762	snp	A/G	3.34846e-05	0.0040916	synonymous-codon, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536330	GACCGCCCGAAGCAG[A/G]TGCTGGACGCCCTGG	4542
rs759407808	snp	C/T	1.66214e-05	0.00288278	missense, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550694	TAACCTGCATAGCAC[C/T]CTGTGGTACAACGGG	4542
rs759457500	snp	A/G	1.68009e-05	0.00289831	missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536253	TCAAACACACTCACC[A/G]ACTCTGGGTTCTTGA	4542
rs759501161	snp	A/G	1.78605e-05	0.0029883	intron-variant	MYO1F	GRCh38.p7	19:8550109	TCAGCTTCCATAAAT[A/G]TTTGTGACCCCAGAG	4542
rs759511634	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8533016	GTCCATAGGTAGCAC[A/G]TTGCTGCTAAGAGCC	4542
rs759522864	snp	A/G	1.97556e-05	0.00314284	intron-variant, missense, utr-variant-3-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536629	GCTGAGTCCCCTCGG[A/G]GTGGGGAGTCACCAG	4542
rs759542383	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8570183	GTTCAAGTGATTCTC[C/T]TGCCTCAGCCTCCCA	4542
rs759559251	snp	C/G	1.69761e-05	0.00291337	intron-variant	MYO1F	GRCh38.p7	19:8544252	AGCCTGGAGCCCTGG[C/G]GGTCTGCGAGGAGGC	4542
rs759601989	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8523590	TCCTGGCCTCAAGCA[A/G]TCCTCCCACTTCGGC	4542
rs759609222	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8559992	GAATTAACACTCAGC[A/G]AGCACCTATGCTGTG	4542
rs759625300	snp	A/T	2.03374e-05	0.00318877	utr-variant-3-prime	MYO1F	GRCh38.p7	19:8521505	AGGCGGGCGAAAGAG[A/T]AGGCAGTATCCCAGG	4542
rs759632182	snp	C/G	3.31592e-05	0.00407167	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554735	GATGAGCACAGAGCC[C/G]ATGTAGGTCTGAGGG	4542
rs759707124	snp	A/G	1.73375e-05	0.00294422	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544409	TCTGCTCCCCCGCCC[A/G]TGGCGTGCATGGTGG	4542
rs759723099	snp	A/C/G/T	9.95289e-05	0.00705387	intron-variant	MYO1F	GRCh38.p7	19:8551955	GCCCTGCCATGCCCC[A/C/G/T]CTAGGTGTTTACCTT	4542
rs759779809	in-del	-/TAG	1.65605e-05	0.0028775	cds-indel, nc-transcript-variant	MYO1F	GRCh38.p7	19:8551813	TGGTTGAGGTAGTAA[-/TAG]TAGTCCGGTGTCATG	4542
rs759787879	snp	A/G	1.7683e-05	0.00297341	synonymous-codon	MYO1F	GRCh38.p7	19:8525558	CATTCCCTTCCGCGT[A/G]GGCTCTGAAAGAAGA	4542
rs759805604	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8565448	TCGGGAGGCTGAGGC[A/G]GGAGAATAGCTTGAA	4542
rs759811979	snp	C/G	3.34292e-05	0.00408821	synonymous-codon	MYO1F	GRCh38.p7	19:8521582	CTGGCCGTGAAGCCG[C/G]CCCTTCCACCAGCCC	4542
rs759894392	snp	C/T	1.65597e-05	0.00287743	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8551854	GTTCTGCCTTTGCTC[C/T]TGGGAGGCCCCTTCC	4542
rs759899326	snp	G/T	2.11947e-05	0.00325529	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550350	AGGTAGGCGGGAAAG[G/T]CCAGGACTACCAGGG	4542
rs759903295	snp	C/T	1.6859e-05	0.00290331	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544332	TGACGAAGCCGGCGC[C/T]CCAGCTGTTGAAATG	4542
rs759960717	in-del	-/T			intron-variant	MYO1F	GRCh38.p7	19:8561431	TCCCTTCCTTTCTCC[-/T]CTCCCTCCCTTCCTT	4542
rs759970049	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8558461	ATGAGACACCTTGCC[G/T]GACCCAGACGACACT	4542
rs760006776	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8557582	GGTGGGATTATAGGC[A/G]TAAGCTACTGCACCC	4542
rs760048213	snp	A/G	0.0020723	0.0321225	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8553150	TTACAAAGCGGCTGG[A/G]ATTGTTGTTGCGCAC	4542
rs760059346	snp	A/G	1.65375e-05	0.0028755	intron-variant	MYO1F	GRCh38.p7	19:8553132	AAGCAGGTCTGCAGA[A/G]ACTTACAAAGCGGCT	4542
rs760080400	snp	C/G	8.39708e-05	0.00647907	intron-variant	MYO1F	GRCh38.p7	19:8539937	TCCCCGTTGTACACC[C/G]CAGGCCCACCTTGAT	4542
rs760082945	snp	A/G	4.97327e-05	0.00498637	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530448	CGCGCCGTTTACCCG[A/G]AGCCTCTCACCTTCC	4542
rs760095446	snp	C/T	5.05847e-05	0.00502889	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550267	TGGACTCGCTGCGCC[C/T]GCCCCAGCGGCTGTC	4542
rs760136277	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8535451	TTCTTTTTGTCTTTT[A/G]TAGAGACAGGGTCTC	4542
rs760147193	snp	A/G	3.35875e-05	0.00409788	missense	MYO1F	GRCh38.p7	19:8525503	GCGCAGGGGCCGCCC[A/G]GGTAGGGGCTTGGGA	4542
rs760178262	snp	C/G	1.65773e-05	0.00287895	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530445	CCCCGCGCCGTTTAC[C/G]CGAAGCCTCTCACCT	4542
rs760201119	snp	A/G	3.54064e-05	0.00420737	intron-variant	MYO1F	GRCh38.p7	19:8555843	CTTGCACGGGGATGC[A/G]GCACCTGGCTCACCG	4542
rs760216978	snp	A/G	1.73045e-05	0.00294142	intron-variant	MYO1F	GRCh38.p7	19:8540051	GGAAAGGGGAGAGGA[A/G]GAGTTGGAGGTATGG	4542
rs760271243	snp	A/G	3.41472e-05	0.00413188	intron-variant	MYO1F	GRCh38.p7	19:8548003	CCCACCCCCACCCCA[A/G]GATCCCCCATCCCTG	4542
rs760285214	snp	A/C	5.03571e-05	0.00501757	intron-variant	MYO1F	GRCh38.p7	19:8539944	TGTACACCCCAGGCC[A/C]ACCTTGATCTTGGAG	4542
rs760297091	snp	G/T	1.65146e-05	0.0028735	intron-variant	MYO1F	GRCh38.p7	19:8553234	CTTTGACGTGCTGGG[G/T]CAGAGGCAGGTGGAG	4542
rs760329455	snp	A/G	1.82168e-05	0.00301795	missense	MYO1F	GRCh38.p7	19:8522518	CACCAGGCACTGGCC[A/G]TTGCCCCACGCTGCG	4542
rs760412275	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8525005	GAGTTCGAGACCAGC[C/G]TGAACAACGTGGTGA	4542
rs760435557	in-del	-/T			downstream-variant-500B	MYO1F	GRCh38.p7	19:8520293	CTTTATTTTCTTTTC[-/T]TTTCTTTTTTTTTTT	4542
rs760465599	snp	A/G	3.31203e-05	0.00406928	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8551795	ACCTGGTAGGTGTCC[A/G]ATTGGTTGAGGTAGT	4542
rs760465699	snp	G/T	3.3134e-05	0.00407012	intron-variant	MYO1F	GRCh38.p7	19:8545751	CCTGGGGTGGAAAAG[G/T]GGGTGGATGTGGGGG	4542
rs760490655	snp	C/T	1.68111e-05	0.00289918	intron-variant	MYO1F	GRCh38.p7	19:8526969	GAGCGTCAGGTGGGA[C/T]ACAGGTGAGGGCGAC	4542
rs760490858	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8556855	TTGTGCCATTGCACT[C/T]CAGCCTTGGCAACAA	4542
rs760499649	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8531196	TTACTAAAAACATAA[A/G]ATTAGCCGGGCATGG	4542
rs760502173	snp	A/G	1.65603e-05	0.00287747	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554542	GTTGTCCGTGAGGGC[A/G]TAGATGTGCGGGGGA	4542
rs760618248	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8546735	CCAGGCTGGAGTGCA[A/G]TGGCACAATCTCGAC	4542
rs760648457	snp	C/T	1.67618e-05	0.00289493	missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536346	TGCTGGACGCCCTGG[C/T]GTTCGTCCCCACGCC	4542
rs760688119	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8558366	TGATGGGGTCTTGCT[C/G]TGTTGCTCAGGCTGG	4542
rs760692798	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8534789	CACCACCACACTTGG[A/C]TAATTTTTTGTATTT	4542
rs760720398	snp	C/G	1.65652e-05	0.0028779	intron-variant	MYO1F	GRCh38.p7	19:8554624	GCCAGGAGTCTGGGG[C/G]CTGTGCCTCCCACCC	4542
rs760740712	snp	A/G	0.000117397	0.00766061	intron-variant, missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536400	AGAATGGCATACCTG[A/G]GGGCGGAGGGCTGGG	4542
rs760846076	snp	A/G	2.26303e-05	0.00336373	intron-variant, synonymous-codon, utr-variant-3-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536637	CCCTCGGGGTGGGGA[A/G]TCACCAGTCCTGGGG	4542
rs760864408	in-del	-/G	0.000167833	0.00915906	intron-variant	MYO1F	GRCh38.p7	19:8536936	AATCTTGGATTGGTT[-/G]GGGGGGGATCACCTG	4542
rs760916904	snp	C/T	1.65963e-05	0.0028806	intron-variant	MYO1F	GRCh38.p7	19:8555607	TCTCCGTCCATGGCC[C/T]AGCCATTCATTCCTT	4542
rs760945904	snp	A/G	1.65759e-05	0.00287883	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530187	TGTGCCCACCCACTA[A/G]TGCCTCACCTTGAAG	4542
rs760952887	snp	G/T	0.000149317	0.00863922	intron-variant	MYO1F	GRCh38.p7	19:8551957	CCTGCCATGCCCCCC[G/T]AGGTGTTTACCTTCC	4542
rs760956064	in-del	-/TG	1.66247e-05	0.00288307	splice-acceptor-variant, intron-variant	MYO1F	GRCh38.p7	19:8550696	ACCTGCATAGCACTC[-/TG]TGGTACAACGGGGGC	4542
rs760958971	snp	C/T	0.000205271	0.0101288	intron-variant	MYO1F	GRCh38.p7	19:8544473	GGGGGCTCTGCGGGG[C/T]GAGCGGGAGCCAGCA	4542
rs760968370	snp	G/T	3.35599e-05	0.00409619	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8539986	GGGGCGCCCCTTCTT[G/T]TCTCCATCCAGCTTC	4542
rs761037694	snp	A/G	3.31373e-05	0.00407032	intron-variant	MYO1F	GRCh38.p7	19:8552018	GCTCCCTCTCCCCCG[A/G]CCCCTTCCCTGCACC	4542
rs761041920	snp	C/T	1.66938e-05	0.00288905	synonymous-codon, missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536552	GCCGGCTCTGCGCAC[C/T]CTGATGTTCTCCTTC	4542
rs761103081	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8568923	GAGACTCCATCTCAA[C/T]AACAACAAATAACCA	4542
rs761125140	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8567974	GGCCCATCAGCCCTC[C/T]TGGCTCTCCCGGCTC	4542
rs761126682	in-del	-/G			intron-variant	MYO1F	GRCh38.p7	19:8554092	GCCTCTTGAGTAGCT[-/G]GGGACTACAGGCGTG	4542
rs761138723	snp	C/G			splice-acceptor-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530366	GCAGGATGTTGGAAG[C/G]TGCGGGGACAGAGGG	4542
rs761149613	snp	A/G	3.31395e-05	0.00407046	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550562	GATACCCACACTCAC[A/G]GTCCACACTCTCCAC	4542
rs761172160	snp	A/C	3.33211e-05	0.0040816	intron-variant	MYO1F	GRCh38.p7	19:8522339	TGTCAGGGTTCTTAC[A/C]ACTCCCCTCACCCCA	4542
rs761223713	snp	C/G	1.78223e-05	0.0029851	splice-acceptor-variant	MYO1F	GRCh38.p7	19:8525563	CCTTCCGCGTAGGCT[C/G]TGAAAGAAGAGTGTC	4542
rs761224553	snp	A/G	2.45053e-05	0.00350029	intron-variant	MYO1F	GRCh38.p7	19:8550377	AGGGCAAAGGTCAGG[A/G]CAAAAATGGGACAGT	4542
rs761238426	snp	C/T	3.52983e-05	0.00420094	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544425	TGGCGTGCATGGTGG[C/T]GCACACGTCGTCCAA	4542
rs761252826	snp	C/T	1.65756e-05	0.00287881	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530435	TGTGCCCCCACCCCG[C/T]GCCGTTTACCCGAAG	4542
rs761278610	snp	A/C	0.000123084	0.00784392	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526440	CCTCTGCCCTAGTTC[A/C]GCGCAGACTCACTGG	4542
rs761281663	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8557413	GCAATCCTTCCACCA[C/T]ACCACAGCCTCCTGG	4542
rs761308378	snp	C/T	0.000397693	0.0140957	missense, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530242	TCGGCGAAGTCCACC[C/T]GCTCCCTCTTGCCCA	4542
rs761313770	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8567317	TGATCCACCTGCCTC[A/G]GCCTCCCAAAGTGCT	4542
rs761328969	snp	A/T			intron-variant	MYO1F	GRCh38.p7	19:8540939	ATTCTGATAGTTCAG[A/T]ATCAGATGCAGATTC	4542
rs761401196	snp	A/T			intron-variant	MYO1F	GRCh38.p7	19:8548006	ACCCCCACCCCAGGA[A/T]CCCCCATCCCTGACT	4542
rs761405883	in-del	-/A			intron-variant	MYO1F	GRCh38.p7	19:8524584	AGCGAGACTGTCTCA[-/A]AAAAAAAAAAAAAAA	4542
rs761411388	snp	A/G	1.80338e-05	0.00300276	intron-variant	MYO1F	GRCh38.p7	19:8540071	TGGAGGTATGGCTAG[A/G]CTTTCGGGTACTCTT	4542
rs761430324	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8552327	TCAGTGGCGCAATGT[C/T]GGCTCACTGCAACGT	4542
rs761433713	snp	C/T	1.68601e-05	0.00290341	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8530549	CATCGAACTTTCGCT[C/T]TCGCACCTCCTCCAG	4542
rs761503537	in-del	-/CA			intron-variant	MYO1F	GRCh38.p7	19:8524582	AGAGCGAGACTGTCT[-/CA]AAAAAAAAAAAAAAA	4542
rs761522033	snp	G/T	0.000701169	0.0187108	intron-variant	MYO1F	GRCh38.p7	19:8553245	TGGGGCAGAGGCAGG[G/T]GGAGTGGGAAGAAGT	4542
rs761577922	snp	A/T			intron-variant	MYO1F	GRCh38.p7	19:8558568	TCTCCTTTTAGCCCG[A/T]CTGAATTTATCTAGT	4542
rs761606405	snp	G/T	1.65622e-05	0.00287764	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8548122	GCTCGAAGCCATTTT[G/T]CTGCAGAAGGAGGAA	4542
rs761606416	snp	A/G	6.71355e-05	0.00579338	synonymous-codon, missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8539965	GATCTTGGAGCCGGC[A/G]GTGCTGGGGCGCCCC	4542
rs761611940	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8550389	AGGGCAAAAATGGGA[C/T]AGTTGGTTGGGCTCT	4542
rs761613616	snp	C/T	6.61026e-05	0.00574865	intron-variant	MYO1F	GRCh38.p7	19:8553342	TCCTTCTGTTTTCCT[C/T]GTCTCACCTGGACCT	4542
rs761619477	snp	A/G	1.66796e-05	0.00288782	synonymous-codon, missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536516	CTGCAGGAATTTGGC[A/G]AACTGGCGGCGGTAG	4542
rs761711607	snp	C/T	1.8601e-05	0.00304962	missense	MYO1F	GRCh38.p7	19:8522529	GGCCGTTGCCCCACG[C/T]TGCGCTTCCTCTGCA	4542
rs761736142	in-del	-/TGGGGAGTCACCAGTCCTGGGGGTGGGTGGGAGGTGCTGGAGGT	3.98057e-05	0.00446109	intron-variant	MYO1F	GRCh38.p7	19:8536631	TGAGTCCCCTCGGGG[lengthTooLong]GGGGGACCTGGGGGG	4542
rs761769729	in-del	-/TCTCCCTCCCTTCCTTCCTCCCT			intron-variant	MYO1F	GRCh38.p7	19:8561431	TCCCTTCCTTTCTCC[-/TCTCCCTCCCTTCCTTCCTCCCT]CTCTCCCTCTCTCTC	4542
rs761802247	snp	C/T	1.67427e-05	0.00289328	intron-variant	MYO1F	GRCh38.p7	19:8548025	CCATCCCTGACTGCT[C/T]GGCCGCCCACCTGCT	4542
rs761805930	snp	A/G	3.34342e-05	0.00408852	intron-variant	MYO1F	GRCh38.p7	19:8527305	AGGGGACAGGTGAGA[A/G]TGACTGTGCGGCAGG	4542
rs761874596	snp	C/T	1.65817e-05	0.00287933	intron-variant	MYO1F	GRCh38.p7	19:8551943	GATCCCTCATCTGCC[C/T]TGCCATGCCCCCCTA	4542
rs761880127	snp	C/G	8.40569e-05	0.00648239	missense	MYO1F	GRCh38.p7	19:8525485	GCTCCTCACCTCTGG[C/G]GGGCGCAGGGGCCGC	4542
rs761915909	snp	C/T	1.65644e-05	0.00287783	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8548275	TGTCCAGCACACCGA[C/T]GCTGTACTCTTCCTG	4542
rs761935761	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8524202	GAGGCGGGTGGATCA[C/T]GAGGTCAGGAGTTCC	4542
rs761984729	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8555136	GTTGCAGCGAGCTAT[C/T]GTGCCATTGCACTCC	4542
rs761986294	snp	A/C	1.6569e-05	0.00287824	missense, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530254	ACCCGCTCCCTCTTG[A/C]CCAGGAACTGACGCA	4542
rs761989166	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8543192	TACAGGCGTGAGCCA[C/T]CACTCCCAGCCTCTC	4542
rs761994355	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8534558	GTGATCCACCACCCT[A/G]GCCTCCCAAAGTGCT	4542
rs761997953	snp	C/T	1.69712e-05	0.00291295	intron-variant	MYO1F	GRCh38.p7	19:8544259	AGCCCTGGGGGTCTG[C/T]GAGGAGGCACAGGGT	4542
rs762039671	snp	C/T	3.40426e-05	0.00412554	missense	MYO1F	GRCh38.p7	19:8522817	GAGGGGGGCACCCCA[C/T]TGCGATCCATGCCTG	4542
rs762039742	snp	C/T	3.31268e-05	0.00406968	missense, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530314	TCCCCGACGAAGTTC[C/T]GATTGATGCTGTTGC	4542
rs762061787	in-del	-/TTCT/TTT			intron-variant	MYO1F	GRCh38.p7	19:8533357	TTCTTCTTCTTCTTC[-/TTCT/TTT]TTTTTTTTTTTTTTT	4542
rs762068979	snp	A/C/G	5.02503e-05	0.00501229	intron-variant	MYO1F	GRCh38.p7	19:8536938	ATCTTGGATTGGTTG[A/C/G]GGGGGATCACCTGTT	4542
rs762080598	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8545989	CTATGAAGCCTCCTC[A/G]AGTCCCAGTGCAGTT	4542
rs762086621	snp	A/T			intron-variant	MYO1F	GRCh38.p7	19:8572565	GAGCCACTGTGCCCG[A/T]GCCCAGTTAGTGGTC	4542
rs762111655	snp	C/G/T	0.000248487	0.011144	intron-variant	MYO1F	GRCh38.p7	19:8555639	CCTGCCTGCCCACCC[C/G/T]CAGCCTTGGCCCAGG	4542
rs762112080	snp	A/G	1.65616e-05	0.00287759	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8552048	CTGGTAGTAGATGTG[A/G]AAGTTCCTCTCATTT	4542
rs762157862	in-del	-/A	1.96173e-05	0.00313181	intron-variant	MYO1F	GRCh38.p7	19:8525593	AGGGAGTTGAATGAC[-/A]AGACAGACCACGCTC	4542
rs762158192	snp	A/G	1.75492e-05	0.00296215	intron-variant	MYO1F	GRCh38.p7	19:8550130	GACCCCAGAGCATCC[A/G]CTCTGCCTTCCAGCC	4542
rs762175522	in-del	-/TTTTTTT			intron-variant	MYO1F	GRCh38.p7	19:8541417	TTGTGTGTGTGTGTG[-/TTTTTTT]TGTGTGTGTTTTTTT	4542
rs762199633	snp	C/T	3.31296e-05	0.00406985	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555706	GGTTGGCGGCAATGG[C/T]GTCTTCGGTGATCTG	4542
rs762338051	snp	A/G	5.02854e-05	0.005014	synonymous-codon, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526535	CAAGTCGCCGAAGCC[A/G]CGGGAGAAGGTGACG	4542
rs762338885	snp	C/T	1.66413e-05	0.0028845	intron-variant	MYO1F	GRCh38.p7	19:8522364	ACCCCAGCTTCTGCC[C/T]TGGTACACACACCTT	4542
rs762362221	snp	A/G	3.38364e-05	0.00411303	intron-variant	MYO1F	GRCh38.p7	19:8521618	ATCTGTGGGAGAGAG[A/G]AAAGCTTGAGGTGCC	4542
rs762388421	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8529219	ATCTCAGTGTGTACC[C/T]GCCACACATAGGCCT	4542
rs762394192	in-del	-/AAA			intron-variant	MYO1F	GRCh38.p7	19:8532155	ATGAAACTCCATCTC[-/AAA]AAAAAAAAAAAGAAA	4542
rs762417931	snp	G/T	2.8571e-05	0.00377951	missense, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526789	TTGGCGGGGCCGTAC[G/T]TGTCGCTGAAGGTGA	4542
rs762421388	snp	C/G/T	3.32941e-05	0.00407997	intron-variant	MYO1F	GRCh38.p7	19:8522355	ACTCCCCTCACCCCA[C/G/T]CTTCTGCCCTGGTAC	4542
rs762452574	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8539120	CCCCATCTCTACTGA[A/C]AATACAAAATTAGGC	4542
rs762469002	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8551210	GCGCATGGCATCATA[C/G]CCGGCTAATCTTTGT	4542
rs762522663	snp	A/G	1.6817e-05	0.0028997	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8536244	GCCTGTCCCTCAAAC[A/G]CACTCACCGACTCTG	4542
rs762560106	snp	A/C	9.93608e-05	0.00704773	intron-variant	MYO1F	GRCh38.p7	19:8545628	AGTGAGACGCCCCCG[A/C]CAAAGTTGACCCAGC	4542
rs762561417	snp	A/G	9.93805e-05	0.00704843	synonymous-codon, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530295	CTCCTCCAGCCCCAG[A/G]TAGTCCCCGACGAAG	4542
rs762571645	snp	A/G	1.66065e-05	0.00288149	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550678	CTGGGCGGGATCCCA[A/G]TAACCTGCATAGCAC	4542
rs762642727	snp	A/C/G	3.31336e-05	0.00407012	stop-gained, synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550584	ACTCTCCACTCGGGC[A/C/G]TAATTCCCGTCTTCA	4542
rs762713864	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8569085	GACAGAAAGCCTGGT[C/G]AATACATACTTGTTG	4542
rs762735746	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8555802	CCTTGCTGCCCTGGG[A/G]GGTGAGAGGGGGGTC	4542
rs762756257	snp	C/T	1.69103e-05	0.00290773	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8530556	CTTTCGCTCTCGCAC[C/T]TCCTCCAGGAGGAAA	4542
rs762759380	snp	C/T	1.65784e-05	0.00287905	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530167	GGCTGTAGTCAGGGT[C/T]TTGCTGTGCCCACCC	4542
rs762780133	snp	C/T	1.65605e-05	0.0028775	intron-variant	MYO1F	GRCh38.p7	19:8548150	GAAAAGGGTCCTTCC[C/T]TCAATGTCCTGGTGC	4542
rs762822978	snp	C/G	3.34924e-05	0.00409208	missense, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8541946	TGAGGTCGGAGAAGA[C/G]AACGTCTCGGTTCCT	4542
rs762959025	in-del	-/TTCCCTTGGCCA	1.68915e-05	0.00290611	cds-indel	MYO1F	GRCh38.p7	19:8525532	ACGACCTCCGAGGTT[-/TTCCCTTGGCCA]TTCCCTTGGCCATTC	4542
rs762996920	snp	C/T	1.73198e-05	0.00294272	synonymous-codon	MYO1F	GRCh38.p7	19:8522696	TGAGGGCGGACGTGC[C/T]CGGGGTCGTCTGCTG	4542
rs763010224	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8553611	GGCATGGTGGCTCCT[A/G]CCTGTAATCCCAGCA	4542
rs763012452	snp	A/C/T	4.72258e-05	0.00485912	utr-variant-3-prime	MYO1F	GRCh38.p7	19:8521497	AGGCAGATAGGCGGG[A/C/T]GAAAGAGAAGGCAGT	4542
rs763029152	snp	A/G	3.31203e-05	0.00406928	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554552	AGGGCGTAGATGTGC[A/G]GGGGATTCTCATACT	4542
rs763032433	snp	A/G	0.000186089	0.00964416	intron-variant	MYO1F	GRCh38.p7	19:8544273	GCGAGGAGGCACAGG[A/G]TAGGGTAGGGGCAGG	4542
rs763036262	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8557112	GCAACATAGTGAGAC[C/T]CCCATCTCTACAAAA	4542
rs763040772	snp	C/T	1.67987e-05	0.00289811	missense	MYO1F	GRCh38.p7	19:8525491	CACCTCTGGGGGGCG[C/T]AGGGGCCGCCCGGGT	4542
rs763107534	snp	G/T	1.67705e-05	0.00289568	intron-variant, missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536410	ACCTGAGGGCGGAGG[G/T]CTGGGGTGTGGGAGT	4542
rs763111087	snp	A/G	1.67638e-05	0.0028951	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550253	GAGGGTCACATTGAT[A/G]GACTCGCTGCGCCCG	4542
rs763161376	in-del	-/AAAG			intron-variant	MYO1F	GRCh38.p7	19:8556487	TCTCTATAAAAAAAG[-/AAAG]AAAGAAAGAAAGAAA	4542
rs763164285	in-del	-/A			intron-variant	MYO1F	GRCh38.p7	19:8556887	GTGAAACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	4542
rs763173854	in-del	-/GA			intron-variant	MYO1F	GRCh38.p7	19:8538583	CATTGCTCCCGGTCT[-/GA]TTTTTTTTTTTTTTT	4542
rs763202102	snp	C/T	3.31268e-05	0.00406968	missense, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530360	TGTTCAGCAGGATGT[C/T]GGAAGCTGCGGGGAC	4542
rs763255973	in-del	-/TGC			intron-variant	MYO1F	GRCh38.p7	19:8543706	TGGTGGTGGTGGTGG[-/TGC]TGGTGGTGGTGGTGG	4542
rs763260710	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8559137	TTCCTGCCTCGATCT[C/T]CCAAACTGCTGGGAT	4542
rs763272747	snp	C/T	1.68519e-05	0.0029027	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544326	GGTGGATGACGAAGC[C/T]GGCGCTCCAGCTGTT	4542
rs763342033	snp	A/G/T	3.38531e-05	0.00411408	intron-variant	MYO1F	GRCh38.p7	19:8548322	CGGTTGATGGCCTGC[A/G/T]GTGTGGGTGGGGACA	4542
rs763342733	in-del	-/TTTC			intron-variant	MYO1F	GRCh38.p7	19:8561606	CCCTCTCTTCTCTTT[-/TTTC]TTTCTCTCTTTCTTT	4542
rs763405821	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8544123	TCAGCCGGAAGGGTC[C/T]GTAGTTCTGGTTAGT	4542
rs763467764	snp	C/G	1.6715e-05	0.00289089	missense	MYO1F	GRCh38.p7	19:8522436	TCGTCCACATCTTGG[C/G]CCACGTACTGGTATA	4542
rs763481998	in-del	-/TTG	4.95872e-05	0.00497907	cds-indel, nc-transcript-variant	MYO1F	GRCh38.p7	19:8553152	ACAAAGCGGCTGGAA[-/TTG]TTGTTGCGCACAGTC	4542
rs763507535	snp	A/G	1.66333e-05	0.00288381	intron-variant	MYO1F	GRCh38.p7	19:8552187	CGAGAGAACCATGTC[A/G]GCACCCCAGTGTCCT	4542
rs763508249	snp	C/T	3.34678e-05	0.00409057	synonymous-codon, missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536957	GGATCACCTGTTCTC[C/T]TCCCAGTCTCGGGGC	4542
rs763572912	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8529485	CAAGCATGAATGCAC[A/G]GGTCAGGTGATGTAT	4542
rs763597561	snp	A/G	1.97627e-05	0.0031434	synonymous-codon, stop-gained, nc-transcript-variant	MYO1F	GRCh38.p7	19:8537044	TGTGGCCACCAGGTC[A/G]TTGGCTTGTTTCTGA	4542
rs763612071	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8549217	TTGACCTCCCAAAGT[G/T]CTGGGATTACAGGCA	4542
rs763614793	snp	A/G	1.73776e-05	0.00294762	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550296	TCCATCTTGCGGCTG[A/G]TCAGCTTCTCCTGCA	4542
rs763652678	snp	C/T	1.65143e-05	0.00287348	intron-variant	MYO1F	GRCh38.p7	19:8553235	TTTGACGTGCTGGGG[C/T]AGAGGCAGGTGGAGT	4542
rs763688012	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8569151	GAGACTGCCCCCTGC[C/T]CTGTCTCCCAGATAT	4542
rs763785570	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8557698	GGCGGGCAGGGCACA[C/G]AGTGCTTGGGGTTCT	4542
rs763800282	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8533237	TTTTGCCATGTTGTC[C/T]AGACTCGTCTGGAAC	4542
rs763829730	snp	A/C	1.84551e-05	0.00303763	synonymous-codon	MYO1F	GRCh38.p7	19:8522525	CACTGGCCGTTGCCC[A/C]ACGCTGCGCTTCCTC	4542
rs763839207	snp	G/T	1.777e-05	0.00298072	intron-variant	MYO1F	GRCh38.p7	19:8555844	TTGCACGGGGATGCG[G/T]CACCTGGCTCACCGA	4542
rs763847411	snp	A/C/T	3.30542e-05	0.00406524	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8553156	AGCGGCTGGAATTGT[A/C/T]GTTGCGCACAGTCTT	4542
rs763925933	snp	C/T	8.45101e-05	0.00649984	intron-variant	MYO1F	GRCh38.p7	19:8548009	CCCACCCCAGGATCC[C/T]CCATCCCTGACTGCT	4542
rs763989154	snp	A/G	1.68869e-05	0.00290571	intron-variant	MYO1F	GRCh38.p7	19:8526986	CAGGTGAGGGCGACA[A/G]GTGAGAGAGACAGAT	4542
rs764028694	snp	C/G/T	8.48844e-05	0.00651431	intron-variant	MYO1F	GRCh38.p7	19:8550396	AAATGGGACAGTTGG[C/G/T]TGGGCTCTTGTGCCT	4542
rs764030240	snp	C/T	1.65649e-05	0.00287788	intron-variant	MYO1F	GRCh38.p7	19:8551730	GACTGGAGTAGAGGC[C/T]GGTGCTCACCAGAGT	4542
rs764117885	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8562244	CTGACCTCGTTACCC[A/G]CCCGCCTTGGCCTCA	4542
rs764217128	snp	A/G	4.95946e-05	0.00497944	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8553368	GACCTTCTCGCCTCC[A/G]CCAGACACCTTGGAG	4542
rs764251554	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8545392	CCGGCATGGAATCTG[C/T]AAATTTGACTCTAAC	4542
rs764270919	in-del	-/AG	5.44835e-05	0.00521908	intron-variant	MYO1F	GRCh38.p7	19:8525571	GTAGGCTCTGAAAGA[-/AG]AGTGTCAGGGAGTTG	4542
rs764273527	snp	C/T	1.73893e-05	0.00294862	missense	MYO1F	GRCh38.p7	19:8522703	GGACGTGCCCGGGGT[C/T]GTCTGCTGGCTCCCA	4542
rs764284948	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8527786	CCCAGCTAATTTTGG[C/T]ATTTTTTGTAGATTC	4542
rs764298485	snp	A/G/T	3.31517e-05	0.00407123	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530188	GTGCCCACCCACTAG[A/G/T]GCCTCACCTTGAAGC	4542
rs764319544	snp	C/T	3.35689e-05	0.00409674	missense, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8541964	CGTCTCGGTTCCTCT[C/T]GCAGAAGCCGCTGAC	4542
rs764376094	snp	C/T	3.34359e-05	0.00408862	synonymous-codon, missense, utr-variant-3-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536564	CACCCTGATGTTCTC[C/T]TTCAGGCCCAGGTAT	4542
rs764387712	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8572360	GCAACCTCTGCCTCT[C/T]GGGTTCAAGCGATTC	4542
rs764453555	in-del	-/C			intron-variant	MYO1F	GRCh38.p7	19:8524582	AGAGCGAGACTGTCT[-/C]AAAAAAAAAAAAAAA	4542
rs764456294	snp	C/T	1.69358e-05	0.00290992	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8527447	GCCCAATCACATACA[C/T]ACACTTGGGCGTCAG	4542
rs764464219	snp	C/T	2.63342e-05	0.00362855	intron-variant, missense, stop-gained, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536641	CGGGGTGGGGAGTCA[C/T]CAGTCCTGGGGGTGG	4542
rs764494302	snp	A/G	0.000211939	0.010292	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544426	GGCGTGCATGGTGGC[A/G]CACACGTCGTCCAAG	4542
rs764500080	snp	A/G	1.6649e-05	0.00288518	intron-variant	MYO1F	GRCh38.p7	19:8554761	GAGGGATGGTTAAGG[A/G]TCGTGTGGTGTCCTG	4542
rs764590088	snp	G/T	3.31724e-05	0.00407248	intron-variant	MYO1F	GRCh38.p7	19:8551964	TGCCCCCCTAGGTGT[G/T]TACCTTCCCATTGTC	4542
rs764619952	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8535924	CTGGCCTTGTGATCC[A/G]CCCTCCTCAGCCTCC	4542
rs764628513	in-del	-/G			intron-variant	MYO1F	GRCh38.p7	19:8560274	CGGATCATGAGGTCA[-/G]GAGATCGAGACCATC	4542
rs764655780	snp	A/G	4.48501e-05	0.0047353	missense, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526545	AAGCCGCGGGAGAAG[A/G]TGACGCTGCGGGTGC	4542
rs764689325	snp	C/G/T	0.000114791	0.00757511	missense, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526458	GCAGACTCACTGGAG[C/G/T]TCTTGGGCAGCCCAT	4542
rs764689507	snp	C/G	1.80863e-05	0.00300713	utr-variant-3-prime	MYO1F	GRCh38.p7	19:8521522	GGCAGTATCCCAGGG[C/G]CCAGCTCAGATCTTC	4542
rs764707091	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8538529	TCAAGTGATCTGCCC[A/G]ATTCAGCCTCTGAAA	4542
rs764738737	snp	C/G	8.39412e-05	0.00647793	missense	MYO1F	GRCh38.p7	19:8521602	TCCACCAGCCCGAGG[C/G]ATCTGTGGGAGAGAG	4542
rs764757771	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8528170	GAGGTTGCAGTGAGC[C/T]GAGATCCTGCCACTG	4542
rs764762806	snp	A/T	1.79512e-05	0.00299588	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544436	GTGGCGCACACGTCG[A/T]CCAAGACGCTCATGA	4542
rs764780651	snp	G/T	5.00221e-05	0.00500085	intron-variant	MYO1F	GRCh38.p7	19:8554772	AAGGGTCGTGTGGTG[G/T]CCTGGTAGGTTTTGT	4542
rs764799983	snp	A/G	1.65688e-05	0.00287821	stop-gained, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550580	CCACACTCTCCACTC[A/G]GGCGTAATTCCCGTC	4542
rs764817909	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8539231	AATAGCCTGGCCAAC[A/G]TGGTGAAACCCTGTC	4542
rs764869179	snp	C/T	1.68943e-05	0.00290635	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8530553	GAACTTTCGCTCTCG[C/T]ACCTCCTCCAGGAGG	4542
rs764885756	snp	A/G	0.00010386	0.00720552	intron-variant	MYO1F	GRCh38.p7	19:8544478	CTCTGCGGGGCGAGC[A/G]GGAGCCAGCAGCGGC	4542
rs764940593	snp	A/G	1.67789e-05	0.00289641	synonymous-codon, missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8539974	GCCGGCGGTGCTGGG[A/G]CGCCCCTTCTTGTCT	4542
rs764990269	snp	G/T	1.65979e-05	0.00288074	intron-variant	MYO1F	GRCh38.p7	19:8550394	AAAAATGGGACAGTT[G/T]GTTGGGCTCTTGTGC	4542
rs764993365	snp	C/G/T	0.000101415	0.00712019	missense, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526477	TGGGCAGCCCATCGC[C/G/T]CACGCTGACCGTGAG	4542
rs765117088	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8564226	TCTCTACTAAAAATA[C/G]AAAAATTAGCCAGGC	4542
rs765188354	snp	G/T	3.30398e-05	0.00406434	intron-variant	MYO1F	GRCh38.p7	19:8553247	GGGCAGAGGCAGGTG[G/T]AGTGGGAAGAAGTCA	4542
rs765236199	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8523753	TCCAACTCTTAGGCT[C/T]ATGATATTCTCCCCT	4542
rs765255091	snp	G/T	1.69844e-05	0.00291409	intron-variant	MYO1F	GRCh38.p7	19:8555813	TGGGGGGTGAGAGGG[G/T]GGTCGGGGTGAGCCC	4542
rs765257989	snp	C/T	1.87016e-05	0.00305785	missense	MYO1F	GRCh38.p7	19:8522532	CGTTGCCCCACGCTG[C/T]GCTTCCTCTGCATGC	4542
rs765299889	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8524283	TAGCTGGGCATGGTG[G/T]TGCATGCCTGTAATC	4542
rs765311016	snp	C/T	1.95574e-05	0.00312703	intron-variant	MYO1F	GRCh38.p7	19:8522622	CTGGAGCTGCCCTCC[C/T]ACCCCACCTACCCGG	4542
rs765342955	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8525293	AGCTGGGTTTGGGTT[C/T]TGAAGGGCTCTGAAT	4542
rs765359209	snp	C/G	1.74921e-05	0.00295732	intron-variant	MYO1F	GRCh38.p7	19:8550133	CCCAGAGCATCCACT[C/G]TGCCTTCCAGCCCCA	4542
rs765435992	snp	C/T	0.000186492	0.00965459	missense	MYO1F	GRCh38.p7	19:8522818	AGGGGGGCACCCCAT[C/T]GCGATCCATGCCTGT	4542
rs765558102	snp	A/G	1.65902e-05	0.00288008	intron-variant	MYO1F	GRCh38.p7	19:8552173	ACTTGCCCTGAATCC[A/G]AGAGAACCATGTCAG	4542
rs765584272	snp	A/G	1.65622e-05	0.00287764	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8552051	GTAGTAGATGTGGAA[A/G]TTCCTCTCATTTTCA	4542
rs765594895	in-del	-/C	1.68238e-05	0.00290028	intron-variant	MYO1F	GRCh38.p7	19:8539905	TAGGGTGGAACTCAG[-/C]CCTCTGCAGGCCCAG	4542
rs765608547	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8535871	TATTTTTAGTAGAGA[C/T]GCGGTTTCACTGTGT	4542
rs765642176	snp	A/G	1.65682e-05	0.00287817	missense, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530257	CGCTCCCTCTTGCCC[A/G]GGAACTGACGCAGCT	4542
rs765663835	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8546847	CCACACCTGGCTAAG[G/T]TTTATATTTTTAGTA	4542
rs765758002	in-del	-/TTCC			intron-variant	MYO1F	GRCh38.p7	19:8561686	TTCTTCCCTTCCCTT[-/TTCC]TTCCTTCCTTCCTTC	4542
rs765795402	in-del	-/CTCCCT	3.3151e-05	0.00407117	intron-variant	MYO1F	GRCh38.p7	19:8552004	GGGCTCCAGGTGGTG[-/CTCCCT]CTCCCCCGGCCCCTT	4542
rs765836759	snp	C/T	3.34538e-05	0.00408971	missense	MYO1F	GRCh38.p7	19:8522440	CCACATCTTGGCCCA[C/T]GTACTGGTATAGGGC	4542
rs765851605	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8561005	GCCTCCCAAAGTGCT[G/T]GGATTATAGGTGTGA	4542
rs765873413	snp	G/T	1.6566e-05	0.00287797	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555718	TGGCGTCTTCGGTGA[G/T]CTGGGGAAGAAGCAC	4542
rs765893368	snp	A/G	1.65649e-05	0.00287788	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555665	CCAGGGTACGAAGAT[A/G]TAGTCGTCCATGAAG	4542
rs765898335	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8537315	TCTACCGCACTCACC[A/G]CTTACCTTGGCACAT	4542
rs765906315	snp	A/G			synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8526791	GGCGGGGCCGTACGT[A/G]TCGCTGAAGGTGAGG	4542
rs765938155	snp	A/G	1.65611e-05	0.00287755	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8552066	GTTCCTCTCATTTTC[A/G]TTTTGCATGACCACG	4542
rs765940060	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8559208	TTTAAAGTGGACTGT[A/G]TTTGCCAGTGGATTC	4542
rs765949900	snp	C/T	1.65608e-05	0.00287752	intron-variant	MYO1F	GRCh38.p7	19:8545634	ACGCCCCCGCCAAAG[C/T]TGACCCAGCCCTCAC	4542
rs766015470	snp	C/T	7.87743e-05	0.00627542	missense, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526570	GGGTGCCGCCACCGC[C/T]CCAGCCCTCCTTCTT	4542
rs766022809	snp	C/T	1.675e-05	0.00289391	missense, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8541949	GGTCGGAGAAGAGAA[C/T]GTCTCGGTTCCTCTC	4542
rs766042063	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8531921	TCAAGAGTTTGAGAC[C/T]AGCCTGGCCAACATG	4542
rs766070344	snp	A/C	1.66139e-05	0.00288213	missense, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550687	ATCCCAATAACCTGC[A/C]TAGCACTCTGTGGTA	4542
rs766100873	snp	C/T	1.66358e-05	0.00288402	missense	MYO1F	GRCh38.p7	19:8522383	TACACACACCTTCCA[C/T]GAGGATCTCAATGAC	4542
rs766114102	snp	C/T	4.38827e-05	0.00468396	intron-variant	MYO1F	GRCh38.p7	19:8544493	GGGAGCCAGCAGCGG[C/T]TCAGTTTGGTCTGCC	4542
rs766119734	snp	C/T	6.88089e-05	0.00586513	intron-variant	MYO1F	GRCh38.p7	19:8530579	GGAGGAAAAGCTGGG[C/T]GGGGGTCGTGGGGGG	4542
rs766248617	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8566267	CTGCCTCCCGGGTTC[A/G]CGCCATTCTCCTGCC	4542
rs766264925	snp	C/T	1.65976e-05	0.00288072	intron-variant	MYO1F	GRCh38.p7	19:8553489	GGGAAGAGCCCTTTT[C/T]AGTGCCTGACCATTC	4542
rs766306914	snp	G/T	1.67643e-05	0.00289515	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8536418	GCGGAGGGCTGGGGT[G/T]TGGGAGTGCTCATAG	4542
rs766319380	snp	A/G	1.65619e-05	0.00287762	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8551742	GGCCGGTGCTCACCA[A/G]AGTCTCACCAAAGTC	4542
rs766330195	snp	A/G	3.66764e-05	0.00428215	intron-variant	MYO1F	GRCh38.p7	19:8540077	TATGGCTAGACTTTC[A/G]GGTACTCTTCCTCCA	4542
rs766412040	in-del	-/TTTCA			intron-variant	MYO1F	GRCh38.p7	19:8534308	GTTGGCTATTTTTCT[-/TTTCA]TTTCTTTTCTTTTCT	4542
rs766471083	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8535572	ACCACACCTGACTTG[G/T]TGCTAGTTTTATTTT	4542
rs766489726	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8546747	GCAATGGCACAATCT[C/T]GACTCACTACAAGCT	4542
rs766516802	snp	C/T	1.65644e-05	0.00287783	intron-variant	MYO1F	GRCh38.p7	19:8554637	GGGCTGTGCCTCCCA[C/T]CCAGCCCCAGCCTCA	4542
rs766520493	snp	A/G	1.656e-05	0.00287745	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8551831	TAGTCCGGTGTCATG[A/G]GGCCCAGGTTCTGCC	4542
rs766576251	snp	A/G	0.000334208	0.0129225	intron-variant	MYO1F	GRCh38.p7	19:8527307	GGGACAGGTGAGAGT[A/G]ACTGTGCGGCAGGTA	4542
rs766600067	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8538242	AAGTCCTGGGATTAC[A/G]GGCTTGAGCCACTGT	4542
rs766616303	snp	C/T	1.67657e-05	0.00289527	synonymous-codon, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536354	GCCCTGGCGTTCGTC[C/T]CCACGCCACCGCGGC	4542
rs766617807	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8557330	GAGACAGGGTCTCAC[C/T]CTGTCACCCAGGCTG	4542
rs766714703	snp	C/T	1.65644e-05	0.00287783	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530369	GGATGTTGGAAGCTG[C/T]GGGGACAGAGGGTGG	4542
rs766761177	snp	C/T	6.62669e-05	0.00575578	missense, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530266	TTGCCCAGGAACTGA[C/T]GCAGCTCGGGCCGCT	4542
rs766767699	snp	C/T	1.67975e-05	0.00289802	missense	MYO1F	GRCh38.p7	19:8525500	GGGGCGCAGGGGCCG[C/T]CCGGGTAGGGGCTTG	4542
rs766772676	in-del	-/G	0.000167833	0.00915906	intron-variant	MYO1F	GRCh38.p7	19:8536937	AATCTTGGATTGGTT[-/G]GGGGGGATCACCTGT	4542
rs766772743	snp	A/G	0.000134522	0.00820016	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550259	CACATTGATGGACTC[A/G]CTGCGCCCGCCCCAG	4542
rs766782618	snp	A/C			missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544305	GGCGCACCTTGCCAG[A/C]GTAGTGGTGGATGAC	4542
rs766812900	snp	G/T	1.69043e-05	0.00290721	intron-variant	MYO1F	GRCh38.p7	19:8544277	GGAGGCACAGGGTAG[G/T]GTAGGGGCAGGGGGC	4542
rs766826421	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8557486	TTTGTATTTTTTTGT[A/G]GAGATGGGGTCTTGC	4542
rs766864768	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8553594	ATCTCTGCTCTCAGC[C/T]GGGCATGGTGGCTCC	4542
rs766885206	snp	C/T	1.66407e-05	0.00288446	intron-variant	MYO1F	GRCh38.p7	19:8552189	AGAGAACCATGTCAG[C/T]ACCCCAGTGTCCTGG	4542
rs766895634	in-del	-/A	1.67438e-05	0.00289338	intron-variant	MYO1F	GRCh38.p7	19:8527295	GAGGGCAGCCAGGGG[-/A]CAGGTGAGAGTGACT	4542
rs766913280	snp	A/G	1.68607e-05	0.00290346	intron-variant	MYO1F	GRCh38.p7	19:8555806	GCTGCCCTGGGGGGT[A/G]AGAGGGGGGTCGGGG	4542
rs766914305	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8569024	CGCCGAGATGCCTCA[A/G]GAAATGTCATCTGTG	4542
rs766914517	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8555328	TGAGCTGAGATTGTG[C/T]CACTACACTCCAGCC	4542
rs766925514	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8531137	AAGATCGCCTGAGGT[C/T]GGGAGTTTGAGACCA	4542
rs766941828	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8541110	TATCTCAGCCTCCCG[A/G]GTAGCTGGGACTATA	4542
rs767003505	snp	C/T	1.6537e-05	0.00287545	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8553143	CAGAGACTTACAAAG[C/T]GGCTGGAATTGTTGT	4542
rs767014430	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8524572	CCTGGGTGACAGAGC[A/G]AGACTGTCTCAAAAA	4542
rs767031556	snp	C/G	1.67061e-05	0.00289011	intron-variant	MYO1F	GRCh38.p7	19:8552198	TGTCAGCACCCCAGT[C/G]TCCTGGGGTGCAGGT	4542
rs767060281	snp	A/G			intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530436	GTGCCCCCACCCCGC[A/G]CCGTTTACCCGAAGC	4542
rs767081806	snp	A/G	5.08169e-05	0.00504042	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550166	CCCACTCGCCTCCAC[A/G]AGGAAGTCGAAGAGG	4542
rs767101273	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8558571	CCTTTTAGCCCGACT[A/G]AATTTATCTAGTGCC	4542
rs767149287	snp	A/G	1.65655e-05	0.00287793	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530383	GCGGGGACAGAGGGT[A/G]GAGGGCAGAGCTCCT	4542
rs767158437	in-del	-/TCGT			intron-variant	MYO1F	GRCh38.p7	19:8561948	CTTGAACTCCTGACC[-/TCGT]TCGTGATCCACCCAT	4542
rs767198149	snp	C/G	1.80589e-05	0.00300485	synonymous-codon	MYO1F	GRCh38.p7	19:8522516	CACACCAGGCACTGG[C/G]CGTTGCCCCACGCTG	4542
rs767200684	in-del	-/TG	3.30398e-05	0.00406434	intron-variant	MYO1F	GRCh38.p7	19:8553266	GGGAAGAAGTCAGAC[-/TG]AGGCAGGAGTGCAGA	4542
rs767221926	snp	C/G	3.53644e-05	0.00420487	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8526832	TCCGCGTCGCCTCCT[C/G]GAAGCGCTTGCACAG	4542
rs767229688	snp	C/T	4.97277e-05	0.00498612	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555745	GCACCATGTCATCCA[C/T]GCCGCTCTGCTTCAC	4542
rs767256717	snp	C/G	1.65603e-05	0.00287747	intron-variant	MYO1F	GRCh38.p7	19:8545640	CCGCCAAAGTTGACC[C/G]AGCCCTCACCAGCTT	4542
rs767293038	snp	C/G	3.98525e-05	0.00446371	missense, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526590	CCCTCCTTCTTCACC[C/G]GAAACTGTAGTCTAT	4542
rs767302243	snp	A/G	1.66374e-05	0.00288417	missense	MYO1F	GRCh38.p7	19:8522394	TCCATGAGGATCTCA[A/G]TGACCTCGTTCACGT	4542
rs767345027	snp	A/C	1.65644e-05	0.00287783	intron-variant	MYO1F	GRCh38.p7	19:8551721	CTGGCCGGGGACTGG[A/C]GTAGAGGCCGGTGCT	4542
rs767357636	in-del	-/TTC			intron-variant	MYO1F	GRCh38.p7	19:8533334	GTGCCCAGCCTCAGA[-/TTC]TTCTTCTTCTTCTTC	4542
rs767398667	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8551454	CCTCCCGTTTTCAAG[C/G]AATTTTCCTGCCTCT	4542
rs767433172	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8569358	TGGGGTAGGAAGGAC[A/G]GGTAGCTTCTTCCTT	4542
rs767444953	snp	A/G	1.68493e-05	0.00290248	stop-gained, nc-transcript-variant	MYO1F	GRCh38.p7	19:8527432	TCTTCACTTTCTCTC[A/G]CCCAATCACATACAC	4542
rs767449105	snp	A/G	9.97556e-05	0.00706172	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8548042	GCCGCCCACCTGCTC[A/G]GCCTTCAGGGTAAGT	4542
rs767449603	snp	C/T	1.65633e-05	0.00287774	intron-variant	MYO1F	GRCh38.p7	19:8554437	TGTTTCAGCAGGGGC[C/T]CGGGCAGCAGGGTCT	4542
rs767476752	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8570304	CGAACTCCTGACCTC[A/G]GGCAATCCACTCATC	4542
rs767491659	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8558090	GTGTCCCTTCACCTT[A/G]CCCCTCAGCAGTGCC	4542
rs767556359	snp	C/T	1.69714e-05	0.00291298	intron-variant	MYO1F	GRCh38.p7	19:8544255	CTGGAGCCCTGGGGG[C/T]CTGCGAGGAGGCACA	4542
rs767709488	snp	A/C	0.000446546	0.0149356	intron-variant	MYO1F	GRCh38.p7	19:8522624	GGAGCTGCCCTCCCA[A/C]CCCACCTACCCGGCC	4542
rs767740984	snp	A/G			utr-variant-3-prime, downstream-variant-500B	MYO1F	GRCh38.p7	19:8520854	GGTCTTGAACTCCTG[A/G]TCTCACGTGATCTGC	4542
rs767816216	in-del	-/T	0.00105727	0.0229677	intron-variant	MYO1F	GRCh38.p7	19:8536683	TGGAGGTGGGGGACC[-/T]GGGGGGATCTGGATT	4542
rs767831999	snp	A/G	1.68724e-05	0.00290446	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544339	GCCGGCGCTCCAGCT[A/G]TTGAAATGCTCGTGG	4542
rs767841692	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8527810	TAGATTCAGGGTTTT[C/G]CCCTGTTGCCCAGGC	4542
rs767845831	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8555176	AACAAGAGCCACTCA[A/G]TCTCAAAAACAAAAC	4542
rs767859102	snp	C/G	1.65597e-05	0.00287743	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8551858	TGCCTTTGCTCCTGG[C/G]AGGCCCCTTCCAGCA	4542
rs767888256	snp	C/T	4.46548e-05	0.00472498	intron-variant	MYO1F	GRCh38.p7	19:8550361	AAAGGCCAGGACTAC[C/T]AGGGCAAAGGTCAGG	4542
rs767929475	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8538347	TCATCCAGGCTGGAG[C/T]GCAGTGGCTCTTGGC	4542
rs767959721	snp	A/G	2.00608e-05	0.00316702	utr-variant-3-prime	MYO1F	GRCh38.p7	19:8521508	CGGGCGAAAGAGAAG[A/G]CAGTATCCCAGGGCC	4542
rs767980126	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8527961	GGGTGCCATGGCTCA[C/T]GCCTGTAATCCCAGC	4542
rs767989345	snp	A/C	1.7468e-05	0.00295528	intron-variant	MYO1F	GRCh38.p7	19:8540059	GAGAGGAGGAGTTGG[A/C]GGTATGGCTAGACTT	4542
rs768027661	snp	G/T			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8577708	AGGAAGCATTTGGGC[G/T]TCCCGGGTCTCTTTT	4542
rs768092586	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8554253	TGAGCCACTACACCT[C/G]GCCTGAGGTGACATT	4542
rs768093806	snp	G/T	3.31241e-05	0.00406952	intron-variant	MYO1F	GRCh38.p7	19:8548212	CAGGGAGGACAGGAT[G/T]TGGGCTGGAGGCAGG	4542
rs768131371	snp	C/G	3.35813e-05	0.0040975	synonymous-codon	MYO1F	GRCh38.p7	19:8525504	CGCAGGGGCCGCCCG[C/G]GTAGGGGCTTGGGAC	4542
rs768144632	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8552942	TGTCATGGCCTCCAC[A/C]GTTCTGCCAATGGGG	4542
rs768230288	snp	A/T	0.000241275	0.0109809	missense	MYO1F	GRCh38.p7	19:8522683	CTGTGTTGTGCTCTG[A/T]GGGCGGACGTGCCCG	4542
rs768317329	snp	G/T	1.65244e-05	0.00287436	intron-variant	MYO1F	GRCh38.p7	19:8553330	CGACCCAGCTTATCC[G/T]TCTGTTTTCCTCGTC	4542
rs768341686	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8563875	CTCAGGTGATCCACC[C/T]GCCTTGGCTTCTCAA	4542
rs768377216	in-del	-/T			intron-variant	MYO1F	GRCh38.p7	19:8567058	TATCACTGGGTCCAA[-/T]TTTTTTTTTTTTTTT	4542
rs768396313	snp	A/G	1.65605e-05	0.0028775	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8551814	GGTTGAGGTAGTAAT[A/G]GTAGTCCGGTGTCAT	4542
rs768444812	snp	C/T	3.45925e-05	0.00415873	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544403	GTCTGGTCTGCTCCC[C/T]CGCCCGTGGCGTGCA	4542
rs768454871	snp	G/T	1.65666e-05	0.00287802	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554695	GGTCGGTGAAGTAGG[G/T]CATCTGCTTGAAGGG	4542
rs768467493	in-del	-/G	1.67365e-05	0.00289275	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8536449	CAGACAGGCCTGGCT[-/G]GGCGTTCTGATGAAG	4542
rs768487934	snp	C/T	1.65666e-05	0.00287802	intron-variant	MYO1F	GRCh38.p7	19:8554625	CCAGGAGTCTGGGGG[C/T]TGTGCCTCCCACCCA	4542
rs768488224	snp	C/T	1.65756e-05	0.00287881	intron-variant	MYO1F	GRCh38.p7	19:8551935	GCCCCTGTGATCCCT[C/T]ATCTGCCCTGCCATG	4542
rs768518378	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8535209	GAGCCAGTGCGCCTG[A/G]CCAGCAAGATTATTT	4542
rs768519468	snp	A/G	2.08388e-05	0.00322784	intron-variant	MYO1F	GRCh38.p7	19:8525603	AATGACAGACAGACC[A/G]CGCTCTTTGCCCCGC	4542
rs768581898	snp	A/T	1.66007e-05	0.00288098	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555765	CTCTGCTTCACGTTG[A/T]GGCTCTGCCAGTGGA	4542
rs768607061	snp	C/T	9.26672e-05	0.00680625	intron-variant, missense, utr-variant-3-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536621	GAGGGTAGGCTGAGT[C/T]CCCTCGGGGTGGGGA	4542
rs768610202	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8576533	CCACCTCTTACTTTG[C/T]GTCTTATGGTGGTAC	4542
rs768646479	snp	C/T	8.35582e-05	0.00646314	missense	MYO1F	GRCh38.p7	19:8521572	AAAGGCCCTCCTGGC[C/T]GTGAAGCCGGCCCTT	4542
rs768646997	in-del	-/GGGGCCGTACCTGGAAGATCTC	1.65625e-05	0.00287766	intron-variant	MYO1F	GRCh38.p7	19:8548226	GTGGGCTGGAGGCAG[-/GGGGCCGTACCTGGAAGATCTC]GGGGCCGTACCTGGA	4542
rs768647960	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8562636	GACGTCCAGGCTCAA[A/G]TGATCCTCCCACCCC	4542
rs768663451	snp	C/G	1.65455e-05	0.00287619	intron-variant	MYO1F	GRCh38.p7	19:8553090	GTGTGTGTGTAGAAA[C/G]GTCAGCACGGAGGGA	4542
rs768686699	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8535564	CATGCGCTACCACAC[C/T]TGACTTGGTGCTAGT	4542
rs768738609	snp	C/G	1.65652e-05	0.0028779	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8552137	CTGGCTCCCCACCTC[C/G]GCTGAACTGGATCTC	4542
rs768739894	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8555070	CATGCCTGTAATCCC[A/G]GCTACTTGGGAGGCT	4542
rs768758519	snp	C/T	1.65638e-05	0.00287778	synonymous-codon, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530301	CAGCCCCAGGTAGTC[C/T]CCGACGAAGTTCCGA	4542
rs768827952	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8557035	TCACACCTGTAATCC[C/T]AGCACTTTGGGAGGC	4542
rs768834213	snp	C/T	1.67579e-05	0.00289459	intron-variant	MYO1F	GRCh38.p7	19:8536925	CTGGGGGGAATGAAT[C/T]TTGGATTGGTTGGGG	4542
rs768847292	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8567609	TGATCCTCCCACCTC[C/G]GCCTCGCAAAGTGCT	4542
rs768854057	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8539579	CCATCCTGGGTGACA[C/G]AGCAAGACTCTGTCT	4542
rs768903358	snp	C/T	1.76608e-05	0.00297155	intron-variant	MYO1F	GRCh38.p7	19:8550125	TTTGTGACCCCAGAG[C/T]ATCCACTCTGCCTTC	4542
rs768916254	snp	C/T	1.65726e-05	0.00287855	synonymous-codon, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530244	GGCGAAGTCCACCCG[C/T]TCCCTCTTGCCCAGG	4542
rs768922091	snp	C/G	1.71655e-05	0.00292958	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8537013	AGCGGATGTAGTGGG[C/G]TGTGCACCTCATCAG	4542
rs768940948	snp	A/G	6.6257e-05	0.00575535	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555704	GAGGTTGGCGGCAAT[A/G]GCGTCTTCGGTGATC	4542
rs768958194	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8560927	TATTTTTGGTAGAGA[C/T]GGGGTTTCACTGTAT	4542
rs768964319	snp	A/C	1.65831e-05	0.00287945	intron-variant	MYO1F	GRCh38.p7	19:8555615	CATGGCCCAGCCATT[A/C]ATTCCTTCCCTGCCT	4542
rs769033261	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8561950	TTGAACTCCTGACCT[C/T]GTGATCCACCCATGT	4542
rs769105319	snp	C/T	1.67371e-05	0.0028928	missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536308	GGTACTGGTCGGGCT[C/T]CATGTTGACCGCCCG	4542
rs769127106	snp	A/T			intron-variant	MYO1F	GRCh38.p7	19:8531864	GGCTCAAGCCTGTAA[A/T]CCCAGCATTTTGGGA	4542
rs769166922	snp	C/T	1.66571e-05	0.00288587	intron-variant	MYO1F	GRCh38.p7	19:8522344	GGGTTCTTACCACTC[C/T]CCTCACCCCAGCTTC	4542
rs769167899	snp	C/T	1.697e-05	0.00291285	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550162	CAGCCCCACTCGCCT[C/T]CACGAGGAAGTCGAA	4542
rs769196533	snp	A/G	1.76384e-05	0.00296966	intron-variant	MYO1F	GRCh38.p7	19:8530620	TCCTGGTGTCTCCCC[A/G]GGGGCTGCAGTTCCG	4542
rs769240858	snp	A/G	1.71811e-05	0.00293091	intron-variant	MYO1F	GRCh38.p7	19:8542035	GGGACTGAGAAACCT[A/G]GCTGGGAGGGTGGGC	4542
rs769241130	snp	C/T	1.68556e-05	0.00290302	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8536222	CTCTCTTCCCCTCTC[C/T]TTCTCTGCCTGTCCC	4542
rs769269236	snp	C/T	4.96849e-05	0.00498397	intron-variant	MYO1F	GRCh38.p7	19:8553465	GGAGGAATAAATGAT[C/T]AGTGGTTGGGGAAGA	4542
rs769327928	snp	A/T	1.68264e-05	0.0029005	intron-variant	MYO1F	GRCh38.p7	19:8548340	GTGGGTGGGGACAGG[A/T]AGTCAGTGGGCATCG	4542
rs769328708	snp	C/T	1.67399e-05	0.00289304	missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536313	TGGTCGGGCTCCATG[C/T]TGACCGCCCGAAGCA	4542
rs769330237	snp	C/T	5.54524e-05	0.00526527	missense, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526528	GCACTGCCAAGTCGC[C/T]GAAGCCGCGGGAGAA	4542
rs769420539	snp	C/T			utr-variant-3-prime	MYO1F	GRCh38.p7	19:8521216	GCACTTTGCCAACAG[C/T]ACAGGACTCAAGACC	4542
rs769422488	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8535193	CTGAGATTACAGGTG[C/T]GAGCCAGTGCGCCTG	4542
rs769435412	snp	G/T	1.67307e-05	0.00289224	missense, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8541934	GCATCAGCTCTATGA[G/T]GTCGGAGAAGAGAAC	4542
rs769475742	snp	A/G	1.65938e-05	0.00288039	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550669	TGCTGGATGCTGGGC[A/G]GGATCCCAATAACCT	4542
rs769512460	snp	C/T	2.31126e-05	0.00339938	synonymous-codon	MYO1F	GRCh38.p7	19:8522759	AGGCCTGTGGGTGCC[C/T]CCTCCAGACATGATC	4542
rs769553424	snp	A/G	1.73975e-05	0.00294931	intron-variant	MYO1F	GRCh38.p7	19:8521650	CTAGCTGGCCCTGGA[A/G]AAAGCTCTCATGCCT	4542
rs769593150	snp	C/T	1.65778e-05	0.002879	intron-variant	MYO1F	GRCh38.p7	19:8551995	CACCCCGCTGGGCTC[C/T]AGGTGGTGCTCCCTC	4542
rs769604235	snp	C/T	3.31735e-05	0.00407255	intron-variant	MYO1F	GRCh38.p7	19:8551946	CCCTCATCTGCCCTG[C/T]CATGCCCCCCTAGGT	4542
rs769634773	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8568643	GCAAGTGGATTTGGC[C/T]GCGCATGGTGGCTCA	4542
rs769682868	snp	A/G	1.65627e-05	0.00287769	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8548241	GGGGGCCGTACCTGG[A/G]AGATCTCGAAGCCGT	4542
rs769691335	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8554837	CTTCCTAAAACTCCA[C/T]TGCTTGGAGGTGGAA	4542
rs769756955	in-del	-/T	1.74394e-05	0.00295286	intron-variant	MYO1F	GRCh38.p7	19:8530601	CGTGGGGGGCAAGGG[-/T]GAGTCCTGGTGTCTC	4542
rs769784805	snp	A/G	1.88638e-05	0.00307108	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550326	AGTCGCCCGCTGTCA[A/G]TGCCCAGCAGGTAGG	4542
rs769790614	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8559195	CAGGATTGAAGTCTT[C/T]AAAGTGGACTGTGTT	4542
rs769799363	snp	C/G	1.65165e-05	0.00287367	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8553189	CGTTGCCGAAGGCCT[C/G]GAGCAGCGGGTTGGA	4542
rs769845393	snp	C/T	1.67047e-05	0.00288999	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550236	GCTGCCTGCTCCACG[C/T]TGAGGGTCACATTGA	4542
rs769862467	in-del	-/TT			intron-variant	MYO1F	GRCh38.p7	19:8546068	CTCTTTTTTTTTTTT[-/TT]TTTTTTTTTTTTTGA	4542
rs769866520	snp	A/C	1.66371e-05	0.00288414	intron-variant	MYO1F	GRCh38.p7	19:8555587	CCTCTGCTCCTTCAC[A/C]CTCCTCTCCGTCCAT	4542
rs769880177	in-del	-/TC			intron-variant	MYO1F	GRCh38.p7	19:8569938	TTTTTTTGGACAGAG[-/TC]TTGTTCTGTTGCCCA	4542
rs769881987	in-del	-/C	5.32496e-05	0.00515965	frameshift-variant	MYO1F	GRCh38.p7	19:8522812	TGGCAGAGGGGGGCA[-/C]CCCATTGCGATCCAT	4542
rs769899272	snp	C/T	6.62504e-05	0.00575507	missense, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530329	CGATTGATGCTGTTG[C/T]GCCTCCGCTCCTTCT	4542
rs769940313	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8567558	GACAAGGTTTTACCG[C/T]GTTGGGCACGCTCAT	4542
rs769946584	snp	A/T			intron-variant	MYO1F	GRCh38.p7	19:8527663	TGTCGCTCAGGCTGG[A/T]GTGCAGTGGTGCCAT	4542
rs769989000	snp	A/C	1.65438e-05	0.00287605	intron-variant	MYO1F	GRCh38.p7	19:8553105	GGTCAGCACGGAGGG[A/C]GCAGCTGCTCCAAGC	4542
rs769996557	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8549190	CTCCTGACCTTGGGT[G/T]ATCTGCCCGCTTTGA	4542
rs770021547	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8575180	CTCCCGGGTTCAAGC[G/T]ATTCTCCTGCCTCAG	4542
rs770023610	in-del	-/TGC			intron-variant	MYO1F	GRCh38.p7	19:8543690	TGGTGGTGGTGGTGG[-/TGC]TGGTGGTGGTGGTGG	4542
rs770047632	snp	C/G	1.68057e-05	0.00289872	missense	MYO1F	GRCh38.p7	19:8525487	TCCTCACCTCTGGGG[C/G]GCGCAGGGGCCGCCC	4542
rs770098017	snp	A/G	3.31307e-05	0.00406992	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555707	GTTGGCGGCAATGGC[A/G]TCTTCGGTGATCTGG	4542
rs770141031	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8531755	ACTATCCACGAGGTA[C/T]ACTGCCGTGTCAGAG	4542
rs770222425	snp	C/T	1.65603e-05	0.00287747	missense, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8545700	TGTTGAAGTACTGGA[C/T]TGGAGTCCAGCGGAT	4542
rs770264867	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8559010	CGGCCTCCTGAGTAG[C/G]TGGCACTACAGGCAC	4542
rs770307042	snp	A/G	1.65663e-05	0.002878	intron-variant	MYO1F	GRCh38.p7	19:8551713	AGGTCTGCCTGGCCG[A/G]GGACTGGAGTAGAGG	4542
rs770317937	snp	C/T	7.74084e-05	0.00622079	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526778	TGGTGCTGGGGTTGG[C/T]GGGGCCGTACGTGTC	4542
rs770373423	snp	A/G	3.31559e-05	0.00407147	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8548308	GTTTCTGCATAGCAC[A/G]GTTGATGGCCTGCGG	4542
rs770415210	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8571944	TAGCCAGGATGGTCT[C/T]GATCTCCTGACTTCG	4542
rs770416547	snp	C/T	6.62416e-05	0.00575469	intron-variant	MYO1F	GRCh38.p7	19:8545626	CCAGTGAGACGCCCC[C/T]GCCAAAGTTGACCCA	4542
rs770418435	snp	C/T	1.65679e-05	0.00287814	intron-variant	MYO1F	GRCh38.p7	19:8551702	TTCTGGGGCTGAGGT[C/T]TGCCTGGCCGGGGAC	4542
rs770438174	snp	A/G	1.65663e-05	0.002878	intron-variant	MYO1F	GRCh38.p7	19:8554605	TCTCAGCCCAGGGCT[A/G]GGGGCCAGGAGTCTG	4542
rs770457876	snp	C/T	1.67688e-05	0.00289554	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8526922	GGAGGATGAAGAAGT[C/T]GTCCTGTCGCGTGCT	4542
rs770476546	in-del	-/CCTCA	3.33136e-05	0.00408114	intron-variant	MYO1F	GRCh38.p7	19:8522344	GGTTCTTACCACTCC[-/CCTCA]CCTCACCCCAGCTTC	4542
rs770511572	snp	C/T			synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8552096	GCGGGACTTCTCCAG[C/T]AAGAAGTTGGAGATC	4542
rs770548153	snp	A/G	1.67758e-05	0.00289614	missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536367	TCCCCACGCCACCGC[A/G]GCCACGTCTCGGGGG	4542
rs770549021	snp	C/T	8.28027e-05	0.00643386	intron-variant	MYO1F	GRCh38.p7	19:8545620	AGGGGACCAGTGAGA[C/T]GCCCCCGCCAAAGTT	4542
rs770549227	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8532782	AGTCCCAGCTATTCC[A/G]GAGGGTGAGGTGGGA	4542
rs770582024	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8545207	ATCCTCCCACCTCAG[A/C]CTTCCGGGTAGCTGG	4542
rs770699540	snp	A/T			intron-variant	MYO1F	GRCh38.p7	19:8539607	TCTCAAAAAAAAAAA[A/T]TATTGGATATTATTA	4542
rs770725359	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8525101	GCTACTCGGGAGGCT[A/G]AGGCAGGAGAATCGC	4542
rs770764911	snp	C/G	1.65633e-05	0.00287774	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8548253	TGGAAGATCTCGAAG[C/G]CGTAAATGTCCAGCA	4542
rs770781915	snp	A/G	1.733e-05	0.00294358	intron-variant	MYO1F	GRCh38.p7	19:8542040	TGAGAAACCTGGCTG[A/G]GAGGGTGGGCGTGGG	4542
rs770781960	snp	A/C	1.68207e-05	0.00290001	intron-variant	MYO1F	GRCh38.p7	19:8525468	ATATAGCAAGGGACG[A/C]AGCTCCTCACCTCTG	4542
rs770786394	snp	A/G	0.000117955	0.00767879	intron-variant	MYO1F	GRCh38.p7	19:8548355	AAGTCAGTGGGCATC[A/G]GTCAGATCTGAAGCC	4542
rs770789416	snp	C/T			utr-variant-3-prime, downstream-variant-500B	MYO1F	GRCh38.p7	19:8520865	CCTGGTCTCACGTGA[C/T]CTGCCCGCCTCAGCC	4542
rs770812629	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8565384	CCCGTCTCCACTAAA[A/G]GTACAACATTAGCCA	4542
rs770815982	snp	A/G	3.24607e-05	0.00402856	synonymous-codon	MYO1F	GRCh38.p7	19:8522785	TGATCTCCAGGGGCA[A/G]GGGGCCCCCTCTGGC	4542
rs770840881	snp	G/T			missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8553201	CCTCGAGCAGCGGGT[G/T]GGACTGCAGGATGAT	4542
rs770889579	snp	A/C/T	3.31257e-05	0.00406962	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8548115	CAAAACTGCTCGAAG[A/C/T]CATTTTTCTGCAGAA	4542
rs770931784	snp	A/C	1.65809e-05	0.00287926	intron-variant	MYO1F	GRCh38.p7	19:8550528	TCACCCACCCACAGG[A/C]CTCCATCCAGCCCTC	4542
rs770942505	snp	C/G/T	5.83633e-05	0.00540174	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544462	CATGATGCCTGGGGG[C/G/T]CTCTGCGGGGCGAGC	4542
rs770943124	snp	G/T	0.000165631	0.00909881	missense, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530294	GCTCCTCCAGCCCCA[G/T]GTAGTCCCCGACGAA	4542
rs770980207	snp	A/G	3.46284e-05	0.00416089	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544405	CTGGTCTGCTCCCCC[A/G]CCCGTGGCGTGCATG	4542
rs771016308	snp	G/T			missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8537030	GTGCACCTCATCAGT[G/T]TGGCCACCAGGTCGT	4542
rs771044972	snp	A/G	1.75164e-05	0.00295937	missense	MYO1F	GRCh38.p7	19:8525556	GCCATTCCCTTCCGC[A/G]TAGGCTCTGAAAGAA	4542
rs771067950	snp	C/T	1.6686e-05	0.00288838	missense, synonymous-codon, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536526	TTGGCGAACTGGCGG[C/T]GGTAGGCGAAGCCGG	4542
rs771082992	in-del	-/TG	3.33297e-05	0.00408213	intron-variant	MYO1F	GRCh38.p7	19:8550719	AACGGGGGCAGAAAC[-/TG]TGCCGTGAATCCTGG	4542
rs771120029	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8559671	AAGAATTAACACGAC[C/T]GGGCGCGGTGGCTCA	4542
rs771130220	snp	A/G	6.17837e-05	0.0055577	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550343	GCCCAGCAGGTAGGC[A/G]GGAAAGGCCAGGACT	4542
rs771170131	snp	C/T	1.66175e-05	0.00288244	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8530500	CGGACAGCCACGTGG[C/T]GCCGCCAGGCCTTCT	4542
rs771174643	snp	A/G	9.94184e-05	0.00704977	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554717	CTTGAAGGGGTTTAC[A/G]GAGATGAGCACAGAG	4542
rs771202309	snp	A/G	0.000281758	0.0118659	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530439	CCCCCACCCCGCGCC[A/G]TTTACCCGAAGCCTC	4542
rs771223190	snp	C/T	2.19508e-05	0.00331284	intron-variant	MYO1F	GRCh38.p7	19:8525608	CAGACAGACCACGCT[C/T]TTTGCCCCGCCCACA	4542
rs771236724	snp	C/T	6.61638e-05	0.00575131	intron-variant	MYO1F	GRCh38.p7	19:8553120	AGCAGCTGCTCCAAG[C/T]AGGTCTGCAGAGACT	4542
rs771318824	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8567143	TTTGGCTTACTGCAA[A/C]CTCCGTCTCCCAGGT	4542
rs771360415	snp	A/G			intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8529994	GTGCCAGGTGAGGGT[A/G]TACCTGTGATGGAAC	4542
rs771367474	snp	G/T	1.74796e-05	0.00295626	missense	MYO1F	GRCh38.p7	19:8522493	CGAGGCTGGGGCTTG[G/T]GTCGGCCCACACCAG	4542
rs771418943	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8548001	ACCCCACCCCCACCC[C/G]AGGATCCCCCATCCC	4542
rs771454462	snp	A/G	1.68607e-05	0.00290346	missense, synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8540014	TTCTCGGGGAAGAGC[A/G]TCCGGAGGAAGGCCC	4542
rs771500300	snp	C/T	1.65685e-05	0.00287819	intron-variant	MYO1F	GRCh38.p7	19:8551924	TGCCTGGCTCAGCCC[C/T]TGTGATCCCTCATCT	4542
rs771505129	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8530936	GTGATCCCAGCTACT[C/T]GGGAGCCTGAGGCAG	4542
rs771534501	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8527555	AGGATCCACCCCAGG[A/C]AGAGGGGTGGTGCTG	4542
rs771536283	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8547497	TAGTCCCAGCTGCTC[A/G]GGAGGCTGAGGCAGG	4542
rs771549992	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8554958	GAAGGCCGAGGCAGG[C/T]GGATCACTTGAGGTC	4542
rs771560841	snp	A/C	0.0578953	0.159987	intron-variant	MYO1F	GRCh38.p7	19:8547991	TGGTCCTTCCACCCC[A/C]CCCCCACCCCAGGAT	4542
rs771587652	in-del	-/CTGGAAGTC			intron-variant	MYO1F	GRCh38.p7	19:8545520	GGTTGTTATCTGTCG[-/CTGGAAGTC]CTGAGTGTAGGGTAG	4542
rs771598971	snp	A/G	1.67013e-05	0.0028897	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8536485	GGCGAGGGCGGGGGT[A/G]GAGGGCTCCTCACCT	4542
rs771632270	snp	A/C	1.65633e-05	0.00287774	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8548103	ACGAAGTTGATGCAA[A/C]ACTGCTCGAAGCCAT	4542
rs771666143	snp	C/T	4.99513e-05	0.00499731	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8527353	CTGAGGGAGACTCCC[C/T]GCAGAGCCTGGATGT	4542
rs771666176	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8544903	GCTTCAGCCTCCTGA[A/G]TAGCTGGGATTACAG	4542
rs771808687	snp	A/G	3.31203e-05	0.00406928	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554534	CGGTACATGTTGTCC[A/G]TGAGGGCGTAGATGT	4542
rs771847570	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8533776	AGCCATGGAGTTTGT[A/G]GAACTTTGTTTCAGC	4542
rs771853880	snp	C/T	5.02273e-05	0.0050111	synonymous-codon, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536318	GGGCTCCATGTTGAC[C/T]GCCCGAAGCAGGTGC	4542
rs771870221	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8547971	TAGTTGCTAAGGGAT[C/G]CTCATGGTCCTTCCA	4542
rs771871972	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8535296	TTCTTATAGGATTTT[A/C]CCACTAAGCATCTGC	4542
rs771881166	snp	A/G	2.03855e-05	0.00319254	utr-variant-3-prime	MYO1F	GRCh38.p7	19:8521479	GCTCCCCACCAGGCC[A/G]GCAGGCAGATAGGCG	4542
rs771898718	snp	A/G/T	3.31303e-05	0.00406992	intron-variant	MYO1F	GRCh38.p7	19:8554623	GGCCAGGAGTCTGGG[A/G/T]GCTGTGCCTCCCACC	4542
rs771916919	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8522964	TAAGGATTGGGCCAG[A/G]CGGAGGGACTCTGCC	4542
rs771930639	snp	C/G	1.67781e-05	0.00289634	synonymous-codon, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536378	CCGCGGCCACGTCTC[C/G]GGGGTCAGAATGGCA	4542
rs772044692	in-del	-/GA	1.68516e-05	0.00290268	intron-variant	MYO1F	GRCh38.p7	19:8555806	GCTGCCCTGGGGGGT[-/GA]GAGGGGGGTCGGGGT	4542
rs772080498	snp	A/G	6.62416e-05	0.00575469	intron-variant	MYO1F	GRCh38.p7	19:8545609	AGACTCAGCTCAGGG[A/G]ACCAGTGAGACGCCC	4542
rs772081337	snp	A/G	3.31285e-05	0.00406978	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555690	ATGAAGCGCTTCCGG[A/G]GGTTGGCGGCAATGG	4542
rs772082774	snp	C/G	2.04509e-05	0.00319766	intron-variant, missense, utr-variant-3-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536632	GAGTCCCCTCGGGGT[C/G]GGGAGTCACCAGTCC	4542
rs772093432	in-del	-/A	2.4536e-05	0.00350248	intron-variant	MYO1F	GRCh38.p7	19:8550379	GGCAAAGGTCAGGGC[-/A]AAAATGGGACAGTTG	4542
rs772094605	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8564933	GCCTGCCACCAAGCC[A/G]GGCTGATTTTTGTGT	4542
rs772130350	snp	A/G	1.67503e-05	0.00289393	synonymous-codon	MYO1F	GRCh38.p7	19:8521594	CCGGCCCTTCCACCA[A/G]CCCGAGGGATCTGTG	4542
rs772170496	snp	A/G	0.000167935	0.00916183	intron-variant	MYO1F	GRCh38.p7	19:8536903	GTTCTAGGGGTAACT[A/G]CAGGGCCTGGGGGGA	4542
rs772218675	snp	C/T			missense, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530203	TGCCTCACCTTGAAG[C/T]GGCGGTCGTACTTGG	4542
rs772227462	snp	C/T	1.66106e-05	0.00288184	intron-variant	MYO1F	GRCh38.p7	19:8555599	CACCCTCCTCTCCGT[C/T]CATGGCCCAGCCATT	4542
rs772244325	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8546598	CCCCCAGGCTCAAGC[A/G]ATCCTCTTAACTTAG	4542
rs772286145	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8558755	ATCCCCAGGCCAGGA[C/G]CTCCTGGAGACAGAG	4542
rs772319398	snp	C/T	1.65751e-05	0.00287876	intron-variant	MYO1F	GRCh38.p7	19:8552004	GGGCTCCAGGTGGTG[C/T]TCCCTCTCCCCCGGC	4542
rs772331130	snp	C/T	1.65718e-05	0.00287848	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550637	GCAAGATCCCCGCCA[C/T]GAGCTGCAGGACCAG	4542
rs772344634	snp	A/G			utr-variant-3-prime	MYO1F	GRCh38.p7	19:8521165	AATGAGCAAAGTCAC[A/G]CTTGTTAAGGACCCC	4542
rs772408876	snp	A/G	6.66811e-05	0.00577374	intron-variant	MYO1F	GRCh38.p7	19:8522329	GCCCGGCCGATGTCA[A/G]GGTTCTTACCACTCC	4542
rs772664504	snp	C/T	0.000167356	0.00914603	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526783	CTGGGGTTGGCGGGG[C/T]CGTACGTGTCGCTGA	4542
rs772716760	snp	C/G	4.37512e-05	0.00467693	missense, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526549	CGCGGGAGAAGGTGA[C/G]GCTGCGGGTGCCGCC	4542
rs772754557	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8559179	GCCACCGCTCCCAGC[A/C]CAGGATTGAAGTCTT	4542
rs772755394	snp	A/C/G	0.000100017	0.00707105	missense, stop-gained, nc-transcript-variant	MYO1F	GRCh38.p7	19:8530525	CCTTCTGGATGGTTC[A/C/G]GGCAAAGCCATCGAA	4542
rs772816513	snp	G/T	1.65968e-05	0.00288065	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550671	CTGGATGCTGGGCGG[G/T]ATCCCAATAACCTGC	4542
rs772831081	in-del	-/AA			intron-variant	MYO1F	GRCh38.p7	19:8524583	GAGCGAGACTGTCTC[-/AA]AAAAAAAAAAAAAAA	4542
rs772854958	snp	C/T	1.65638e-05	0.00287778	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8548248	GTACCTGGAAGATCT[C/T]GAAGCCGTAAATGTC	4542
rs772879008	snp	C/G	1.68278e-05	0.00290062	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8536237	CTTCTCTGCCTGTCC[C/G]TCAAACACACTCACC	4542
rs772926234	snp	A/C	1.72291e-05	0.002935	intron-variant	MYO1F	GRCh38.p7	19:8542037	GACTGAGAAACCTGG[A/C]TGGGAGGGTGGGCGT	4542
rs773051503	snp	A/G	0.000117132	0.00765195	synonymous-codon, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8541938	CAGCTCTATGAGGTC[A/G]GAGAAGAGAACGTCT	4542
rs773071451	in-del	-/C			intron-variant	MYO1F	GRCh38.p7	19:8557110	GGCAACATAGTGAGA[-/C]CCCCCATCTCTACAA	4542
rs773074453	snp	A/G	8.63998e-05	0.0065721	missense	MYO1F	GRCh38.p7	19:8522692	GCTCTGAGGGCGGAC[A/G]TGCCCGGGGTCGTCT	4542
rs773136789	snp	C/G	1.66007e-05	0.00288098	intron-variant	MYO1F	GRCh38.p7	19:8551951	ATCTGCCCTGCCATG[C/G]CCCCCTAGGTGTTTA	4542
rs773140686	snp	C/T	1.6851e-05	0.00290263	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544325	TGGTGGATGACGAAG[C/T]CGGCGCTCCAGCTGT	4542
rs773197400	snp	C/T	0.000142352	0.00843539	synonymous-codon	MYO1F	GRCh38.p7	19:8522762	CCTGTGGGTGCCCCC[C/T]CCAGACATGATCTCC	4542
rs773206689	snp	C/T	1.72098e-05	0.00293336	synonymous-codon	MYO1F	GRCh38.p7	19:8525549	TCCCTTGGCCATTCC[C/T]TTCCGCGTAGGCTCT	4542
rs773215733	snp	C/T	0.000149684	0.00864984	intron-variant	MYO1F	GRCh38.p7	19:8555588	CTCTGCTCCTTCACC[C/T]TCCTCTCCGTCCATG	4542
rs773222671	snp	A/G	4.97451e-05	0.00498699	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530148	GGGCCAGGTGAGGGT[A/G]CCAGGCTGTAGTCAG	4542
rs773226691	snp	C/G	4.96808e-05	0.00498377	intron-variant	MYO1F	GRCh38.p7	19:8548141	CAGAAGGAGGAAAAG[C/G]GTCCTTCCCTCAATG	4542
rs773285600	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8552464	ATTTTTGTATTTTTC[A/G]TCATGTTGGCCAGGC	4542
rs773317442	snp	C/T	9.6857e-05	0.00695838	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550331	CCCGCTGTCAATGCC[C/T]AGCAGGTAGGCGGGA	4542
rs773364874	snp	C/G	1.65425e-05	0.00287593	intron-variant	MYO1F	GRCh38.p7	19:8553109	AGCACGGAGGGAGCA[C/G]CTGCTCCAAGCAGGT	4542
rs773374975	in-del	-/G	0.00010082	0.00709928	intron-variant	MYO1F	GRCh38.p7	19:8536912	GTAACTGCAGGGCCT[-/G]GGGGGAATGAATCTT	4542
rs773388614	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8558195	TTGAGTCAGAGTCTT[G/T]TTCTGTCACCCAGGC	4542
rs773405214	snp	A/C/T	5.19299e-05	0.00509536	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544404	TCTGGTCTGCTCCCC[A/C/T]GCCCGTGGCGTGCAT	4542
rs773442534	snp	A/G	3.36095e-05	0.00409922	missense	MYO1F	GRCh38.p7	19:8525488	CCTCACCTCTGGGGG[A/G]CGCAGGGGCCGCCCG	4542
rs773488128	snp	A/G	1.67708e-05	0.00289571	intron-variant, missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536406	GCATACCTGAGGGCG[A/G]AGGGCTGGGGTGTGG	4542
rs773509348	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8546653	GTGTGAGTGATTGTG[C/T]CTGGCTCGGTCTGTC	4542
rs773560843	snp	A/C	6.64308e-05	0.0057629	intron-variant	MYO1F	GRCh38.p7	19:8552180	CTGAATCCGAGAGAA[A/C]CATGTCAGCACCCCA	4542
rs773563083	snp	C/T	3.34644e-05	0.00409036	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555793	GGAAGCGCTCCTTGC[C/T]GCCCTGGGGGGTGAG	4542
rs773570258	snp	C/T	1.66818e-05	0.00288802	synonymous-codon	MYO1F	GRCh38.p7	19:8522426	GAAGCTCAGCTCGTC[C/T]ACATCTTGGCCCACG	4542
rs773592872	snp	A/G	1.67433e-05	0.00289333	intron-variant	MYO1F	GRCh38.p7	19:8536942	TGGATTGGTTGGGGG[A/G]GATCACCTGTTCTCC	4542
rs773662654	snp	A/G	9.93739e-05	0.0070482	missense, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530330	GATTGATGCTGTTGC[A/G]CCTCCGCTCCTTCTT	4542
rs773677223	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8539181	GCGCTTTGGGAGGCT[A/G]AGGCAGGCGGATCAC	4542
rs773707121	snp	C/G	4.96808e-05	0.00498377	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8551781	CGTCCGTGCCGTCCA[C/G]CTGGTAGGTGTCCGA	4542
rs773743721	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8563655	CTGGGGTTACAGGAG[C/T]CCATCAACACGCCCA	4542
rs773746108	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8549893	GCAGCCCCAACCTCC[G/T]GGGTTCAAATGATCC	4542
rs773782916	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8552307	TCTGTTGCTCAGGCT[A/G]GGATTCAGTGGCGCA	4542
rs773792789	snp	A/C	0.102504	0.201854	intron-variant	MYO1F	GRCh38.p7	19:8547997	TTCCACCCCACCCCC[A/C]CCCCAGGATCCCCCA	4542
rs773798417	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8564984	CACCACGTTGGACAC[A/G]CTCATCTCGAACTCC	4542
rs773881396	snp	A/C	3.31214e-05	0.00406935	missense, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8545717	GGAGTCCAGCGGATG[A/C]CTTCCTGCACATACT	4542
rs773888828	snp	A/G	3.31203e-05	0.00406928	missense, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8545702	TTGAAGTACTGGATT[A/G]GAGTCCAGCGGATGC	4542
rs773897127	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8540883	GCATCCTGGCTTAAA[G/T]ATCAGGTTAGGTTCC	4542
rs773897875	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8571966	CTGACTTCGTGATCC[G/T]CACGCCTCGGCCTCC	4542
rs773911242	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8544114	CCTGGGGGGTCAGCC[G/T]GAAGGGTCTGTAGTT	4542
rs773928816	snp	C/T	1.65603e-05	0.00287747	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554526	GCATGTTCCGGTACA[C/T]GTTGTCCGTGAGGGC	4542
rs773952767	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8540190	GTTGGTTTTTTGGTT[G/T]GTTTTTTGAGGCAGG	4542
rs773978862	snp	C/G	5.04401e-05	0.0050217	splice-donor-variant	MYO1F	GRCh38.p7	19:8525478	GGACGCAGCTCCTCA[C/G]CTCTGGGGGGCGCAG	4542
rs773997297	snp	A/C	1.69841e-05	0.00291407	intron-variant	MYO1F	GRCh38.p7	19:8544246	GGCTACAGCCTGGAG[A/C]CCTGGGGGTCTGCGA	4542
rs774014268	snp	C/T	2.03834e-05	0.00319238	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8526816	GTGAGGGGCAGGGGC[C/T]TCCGCGTCGCCTCCT	4542
rs774064750	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8534530	CAGGCTGGTCTCGAA[C/T]TCCTAACCTCAAGTG	4542
rs774066426	snp	C/T	6.70995e-05	0.00579182	synonymous-codon, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536372	ACGCCACCGCGGCCA[C/T]GTCTCGGGGGTCAGA	4542
rs774076527	snp	G/T	0.000314687	0.0125397	intron-variant	MYO1F	GRCh38.p7	19:8551715	GTCTGCCTGGCCGGG[G/T]ACTGGAGTAGAGGCC	4542
rs774085688	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8540674	GAGATCGTGCCACTG[C/T]ACTCCAGCCTGGGCG	4542
rs774138875	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8539610	CAAAAAAAAAAATTA[C/T]TGGATATTATTAAGA	4542
rs774181990	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8546572	ACTATGTTGTCCAGG[C/T]TGGCTTTGAACCCCC	4542
rs774189690	snp	A/C			synonymous-codon	MYO1F	GRCh38.p7	19:8521579	CTCCTGGCCGTGAAG[A/C]CGGCCCTTCCACCAG	4542
rs774252995	snp	A/G	3.34297e-05	0.00408824	missense	MYO1F	GRCh38.p7	19:8521581	CCTGGCCGTGAAGCC[A/G]GCCCTTCCACCAGCC	4542
rs774293839	in-del	-/GACA	7.72365e-05	0.00621388	intron-variant	MYO1F	GRCh38.p7	19:8525591	GTCAGGGAGTTGAAT[-/GACA]GACAGACCACGCTCT	4542
rs774342013	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8551264	ACTATGTTGGCCAGG[A/C]TGGTCTTGAACTCCT	4542
rs774373182	snp	A/G	0.000215294	0.0103731	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8548255	GAAGATCTCGAAGCC[A/G]TAAATGTCCAGCACA	4542
rs774438073	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8568657	CCGCGCATGGTGGCT[C/T]ACGCCTGTAATCCCA	4542
rs774500152	snp	A/G	4.17868e-05	0.00457074	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550345	CCAGCAGGTAGGCGG[A/G]AAAGGCCAGGACTAC	4542
rs774505037	in-del	-/G	1.67287e-05	0.00289207	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8536464	GGGCGTTCTGATGAA[-/G]GGGATGGCGAGGGCG	4542
rs774564677	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8565330	GGCAGATCAACTGAG[A/G]TTGGGAGTTTGAGAC	4542
rs774610076	snp	C/T	5.04096e-05	0.00502018	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8527424	AGGTCCCTTCTTCAC[C/T]TTCTCTCGCCCAATC	4542
rs774634758	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8529138	GCCACATAAACTTGT[C/T]CAAGGTAGGTGAGGG	4542
rs774691456	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8567695	AACTACAGCACAGAG[A/G]GGTTAAGTGTCCTCT	4542
rs774694675	snp	C/T	6.72981e-05	0.00580039	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550263	TTGATGGACTCGCTG[C/T]GCCCGCCCCAGCGGC	4542
rs774720685	in-del	-/CTCTCC/CTCTCTCTCC			intron-variant	MYO1F	GRCh38.p7	19:8553922	TCTCTCTCTCTCTCT[-/CTCTCC/CTCTCTCTCC]CGCTCTCTTTCTCTC	4542
rs774761610	snp	C/T	1.65641e-05	0.00287781	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554654	CAGCCCCAGCCTCAC[C/T]GCGCCCTGATAGAGG	4542
rs774776542	snp	A/G	1.65119e-05	0.00287327	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8553210	GCGGGTTGGACTGCA[A/G]GATGATATCTTTGAC	4542
rs774797982	snp	C/T	1.65776e-05	0.00287898	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530444	ACCCCGCGCCGTTTA[C/T]CCGAAGCCTCTCACC	4542
rs774840348	snp	C/T	1.6563e-05	0.00287771	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8548110	TGATGCAAAACTGCT[C/T]GAAGCCATTTTTCTG	4542
rs774844121	snp	C/T	1.65468e-05	0.00287631	missense	MYO1F	GRCh38.p7	19:8525557	CCATTCCCTTCCGCG[C/T]AGGCTCTGAAAGAAG	4542
rs774859714	in-del	-/GTGGCA			intron-variant	MYO1F	GRCh38.p7	19:8544031	GCGGTGGCGGTGGCG[-/GTGGCA]GTGGCGGTGCTGGTG	4542
rs774869032	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8533504	GGACTACAGGCGCCC[A/G]CCACCATGCCTGGCT	4542
rs774928281	snp	C/G	1.70371e-05	0.0029186	intron-variant	MYO1F	GRCh38.p7	19:8540032	CGGAGGAAGGCCCTG[C/G]GTAGGAAAGGGGAGA	4542
rs774933008	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8539112	TGGTGAAACCCCATC[C/T]CTACTGAAAATACAA	4542
rs774935688	snp	C/T	0.000164484	0.00906724	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550342	TGCCCAGCAGGTAGG[C/T]GGGAAAGGCCAGGAC	4542
rs774970775	snp	A/G	3.47802e-05	0.00417	intron-variant	MYO1F	GRCh38.p7	19:8555835	GGTGAGCCCTTGCAC[A/G]GGGATGCGGCACCTG	4542
rs774986105	in-del	-/GA			intron-variant	MYO1F	GRCh38.p7	19:8556499	AGAAAGAAAGAAAGA[-/GA]AAGAAAGAGAAAGAA	4542
rs775106804	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8523001	AGGGCCTAGACAGAA[A/G]CTTTTTTAAGCATAA	4542
rs775180613	snp	A/G	1.65776e-05	0.00287898	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530447	CCGCGCCGTTTACCC[A/G]AAGCCTCTCACCTTC	4542
rs775216667	snp	C/G	1.67981e-05	0.00289806	intron-variant	MYO1F	GRCh38.p7	19:8526956	GAGGGGCGGGTGAGA[C/G]CGTCAGGTGGGACAC	4542
rs775238505	snp	A/C	1.83886e-05	0.00303216	intron-variant	MYO1F	GRCh38.p7	19:8548002	CCCCACCCCCACCCC[A/C]GGATCCCCCATCCCT	4542
rs775262419	snp	C/T	3.31318e-05	0.00406999	intron-variant	MYO1F	GRCh38.p7	19:8551723	GGCCGGGGACTGGAG[C/T]AGAGGCCGGTGCTCA	4542
rs775316073	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8548426	TGGGTGATGTCCCCT[C/T]ATGCCAGTTTCCCTC	4542
rs775374729	snp	A/G	3.31559e-05	0.00407147	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530179	GGTCTTGCTGTGCCC[A/G]CCCACTAGTGCCTCA	4542
rs775391540	in-del	-/TT	0.000812155	0.020135	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8536212	ATACCTTTCTCTCTC[-/TT]CCCCTCTCCTTCTCT	4542
rs775403459	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8570347	AGTGCTGGGATTATA[A/G]GCGTGAGCCACTGCA	4542
rs775459301	snp	C/T	4.968e-05	0.00498373	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554541	TGTTGTCCGTGAGGG[C/T]GTAGATGTGCGGGGG	4542
rs775468756	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8561039	ACTGCGCCTGGCCAC[A/G]CCTGGCTAATTTTTA	4542
rs775498334	snp	A/G	1.67649e-05	0.0028952	intron-variant	MYO1F	GRCh38.p7	19:8536919	CAGGGCCTGGGGGGA[A/G]TGAATCTTGGATTGG	4542
rs775501333	snp	A/C/G	0.000173363	0.00930878	missense	MYO1F	GRCh38.p7	19:8522698	AGGGCGGACGTGCCC[A/C/G]GGGTCGTCTGCTGGC	4542
rs775516250	in-del	-/G	1.68196e-05	0.00289992	frameshift-variant	MYO1F	GRCh38.p7	19:8525482	CAGCTCCTCACCTCT[-/G]GGGGGGCGCAGGGGC	4542
rs775544249	snp	G/T	3.33239e-05	0.00408177	intron-variant	MYO1F	GRCh38.p7	19:8522331	CCGGCCGATGTCAGG[G/T]TTCTTACCACTCCCC	4542
rs775670923	snp	C/G			missense, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530325	GTTCCGATTGATGCT[C/G]TTGCGCCTCCGCTCC	4542
rs775692519	snp	A/C	6.62427e-05	0.00575473	intron-variant	MYO1F	GRCh38.p7	19:8545612	CTCAGCTCAGGGGAC[A/C]AGTGAGACGCCCCCG	4542
rs775694491	snp	A/G	2.14941e-05	0.0032782	intron-variant, missense, utr-variant-3-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536635	TCCCCTCGGGGTGGG[A/G]AGTCACCAGTCCTGG	4542
rs775704886	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8553549	AGTATTCCGGGTACT[A/G]GGGATACTGTAATGA	4542
rs775706661	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8567569	ACCGCGTTGGGCACG[C/T]TCATCTCGAACTCCC	4542
rs775707003	snp	C/T	3.31483e-05	0.004071	missense, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530240	AATCGGCGAAGTCCA[C/T]CCGCTCCCTCTTGCC	4542
rs775710348	snp	A/G	3.31367e-05	0.00407029	intron-variant	MYO1F	GRCh38.p7	19:8552017	TGCTCCCTCTCCCCC[A/G]GCCCCTTCCCTGCAC	4542
rs775743787	snp	C/T	1.66073e-05	0.00288156	intron-variant	MYO1F	GRCh38.p7	19:8554752	TGTAGGTCTGAGGGA[C/T]GGTTAAGGGTCGTGT	4542
rs775772212	in-del	-/A			intron-variant	MYO1F	GRCh38.p7	19:8559952	AAAACTCCATCTCAG[-/A]AAAAAAAAAAAAAAA	4542
rs775802847	snp	C/T	1.74631e-05	0.00295487	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544419	CGCCCGTGGCGTGCA[C/T]GGTGGCGCACACGTC	4542
rs775809521	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8527701	CACTGCAACCTCCCC[C/G]TCCTGGGCTTGAGTG	4542
rs775876842	snp	A/T			intron-variant	MYO1F	GRCh38.p7	19:8559043	ACCACTAAGCCCAGC[A/T]AATTTTTTGTATTTT	4542
rs775887631	snp	C/G	0.00016334	0.00903566	intron-variant	MYO1F	GRCh38.p7	19:8550370	GACTACCAGGGCAAA[C/G]GTCAGGGCAAAAATG	4542
rs775892609	snp	A/G	2.02141e-05	0.00317909	intron-variant	MYO1F	GRCh38.p7	19:8544470	CTGGGGGGCTCTGCG[A/G]GGCGAGCGGGAGCCA	4542
rs775985136	snp	C/T	0.000301644	0.0122773	synonymous-codon	MYO1F	GRCh38.p7	19:8521597	GCCCTTCCACCAGCC[C/T]GAGGGATCTGTGGGA	4542
rs776059662	snp	C/G	6.14912e-05	0.00554453	missense, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526520	AACCTTGAGCACTGC[C/G]AAGTCGCCGAAGCCG	4542
rs776066516	snp	C/G	1.6736e-05	0.0028927	intron-variant	MYO1F	GRCh38.p7	19:8541894	GAGGTCCCCATGCCT[C/G]GGACCACTCACTGCT	4542
rs776075685	snp	G/T	1.76799e-05	0.00297315	intron-variant	MYO1F	GRCh38.p7	19:8530624	GGTGTCTCCCCAGGG[G/T]CTGCAGTTCCGGGTT	4542
rs776091307	snp	C/G/T	3.30487e-05	0.00406491	intron-variant	MYO1F	GRCh38.p7	19:8553329	GCGACCCAGCTTATC[C/G/T]TTCTGTTTTCCTCGT	4542
rs776196217	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8523686	TAGAGACAGGGTTTT[A/G]CTCTGTGGCCCAGGA	4542
rs776204655	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8567285	TTGGCCAGGCTGGTC[C/T]TGAACTCCTGACCTT	4542
rs776218246	in-del	-/C			intron-variant	MYO1F	GRCh38.p7	19:8552706	GATTTTTTTCCCCCC[-/C]AGGCTACACAGCTCA	4542
rs776258177	snp	A/C	1.65789e-05	0.0028791	intron-variant	MYO1F	GRCh38.p7	19:8551936	CCCCTGTGATCCCTC[A/C]TCTGCCCTGCCATGC	4542
rs776265574	snp	A/G			synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550241	CTGCTCCACGTTGAG[A/G]GTCACATTGATGGAC	4542
rs776267777	snp	G/T	8.78387e-05	0.00662659	intron-variant	MYO1F	GRCh38.p7	19:8540065	AGGAGTTGGAGGTAT[G/T]GCTAGACTTTCGGGT	4542
rs776267879	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8562074	GAGTCTTGCTCTGTC[A/G]CCCAGGCTGAAGGGC	4542
rs776274799	snp	C/T	1.65252e-05	0.00287443	intron-variant	MYO1F	GRCh38.p7	19:8553333	CCCAGCTTATCCTTC[C/T]GTTTTCCTCGTCTCA	4542
rs776289673	snp	A/T			utr-variant-3-prime	MYO1F	GRCh38.p7	19:8521168	GAGCAAAGTCACGCT[A/T]GTTAAGGACCCCCCC	4542
rs776353331	snp	C/G	2.02239e-05	0.00317986	intron-variant	MYO1F	GRCh38.p7	19:8522612	TGCCCACCTCCTGGA[C/G]CTGCCCTCCCACCCC	4542
rs776453460	snp	G/T	1.65679e-05	0.00287814	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554701	TGAAGTAGGGCATCT[G/T]CTTGAAGGGGTTTAC	4542
rs776464853	snp	A/G	0.000115935	0.00761277	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8548117	AAACTGCTCGAAGCC[A/G]TTTTTCTGCAGAAGG	4542
rs776499586	in-del	-/GTG	3.85171e-05	0.00438829	splice-acceptor-variant	MYO1F	GRCh38.p7	19:8522548	CTTCCTCTGCATGCT[-/GTG]GTGGGCACAGGGGGT	4542
rs776531446	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8555238	AGCCAGGCATGGTGG[C/T]GCATGCCTATAATCC	4542
rs776557240	in-del	-/CCT			intron-variant	MYO1F	GRCh38.p7	19:8561592	TTCCTTCCCTCCCTC[-/CCT]CTCTTCTCTTTTTTC	4542
rs776561813	snp	A/G	1.65655e-05	0.00287793	intron-variant	MYO1F	GRCh38.p7	19:8554629	GAGTCTGGGGGCTGT[A/G]CCTCCCACCCAGCCC	4542
rs776629967	snp	C/T	1.65638e-05	0.00287778	missense, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530303	GCCCCAGGTAGTCCC[C/T]GACGAAGTTCCGATT	4542
rs776630100	snp	G/T	5.22753e-05	0.00511223	missense	MYO1F	GRCh38.p7	19:8522809	CTCTGGCAGAGGGGG[G/T]CACCCCATTGCGATC	4542
rs776647055	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8537922	TGGAGGTAGGGAAAC[G/T]GTGTGTATGCCTGAG	4542
rs776718917	snp	C/T	1.66843e-05	0.00288823	missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536515	TCTGCAGGAATTTGG[C/T]GAACTGGCGGCGGTA	4542
rs776728492	snp	A/C	1.74573e-05	0.00295438	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8537019	TGTAGTGGGGTGTGC[A/C]CCTCATCAGTGTGGC	4542
rs776736885	snp	A/G	3.31329e-05	0.00407005	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8552141	CTCCCCACCTCGGCT[A/G]AACTGGATCTCAAAG	4542
rs776763487	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8524187	GCAGTTTGGGAGGCC[A/G]AGGCGGGTGGATCAC	4542
rs776764087	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8535574	CACACCTGACTTGGT[G/T]CTAGTTTTATTTTGC	4542
rs776771185	snp	A/G	3.3129e-05	0.00406982	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555705	AGGTTGGCGGCAATG[A/G]CGTCTTCGGTGATCT	4542
rs776809328	snp	A/G	0.000115918	0.0076122	intron-variant	MYO1F	GRCh38.p7	19:8548154	AGGGTCCTTCCCTCA[A/G]TGTCCTGGTGCTGGA	4542
rs776818989	snp	A/G	3.52348e-05	0.00419716	intron-variant	MYO1F	GRCh38.p7	19:8550126	TTGTGACCCCAGAGC[A/G]TCCACTCTGCCTTCC	4542
rs776825881	snp	C/T	3.34124e-05	0.00408719	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550234	AGGCTGCCTGCTCCA[C/T]GTTGAGGGTCACATT	4542
rs776840290	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8563138	CTGGGACTACAGGCA[A/C]CTGCCACCATGCCTG	4542
rs776848982	snp	G/T	4.96857e-05	0.00498401	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8552045	CACCTGGTAGTAGAT[G/T]TGGAAGTTCCTCTCA	4542
rs776863768	snp	C/G	1.6569e-05	0.00287824	synonymous-codon, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530253	CACCCGCTCCCTCTT[C/G]CCCAGGAACTGACGC	4542
rs776907360	snp	A/G	1.69654e-05	0.00291246	intron-variant	MYO1F	GRCh38.p7	19:8544258	GAGCCCTGGGGGTCT[A/G]CGAGGAGGCACAGGG	4542
rs776984727	snp	G/T	5.21499e-05	0.0051061	synonymous-codon, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526532	TGCCAAGTCGCCGAA[G/T]CCGCGGGAGAAGGTG	4542
rs777036772	snp	C/T	1.65677e-05	0.00287812	intron-variant	MYO1F	GRCh38.p7	19:8555637	TCCCTGCCTGCCCAC[C/T]CCCAGCCTTGGCCCA	4542
rs777097779	snp	C/G	1.66551e-05	0.00288571	intron-variant	MYO1F	GRCh38.p7	19:8522346	GTTCTTACCACTCCC[C/G]TCACCCCAGCTTCTG	4542
rs777098318	snp	A/T	3.31345e-05	0.00407016	synonymous-codon, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530265	CTTGCCCAGGAACTG[A/T]CGCAGCTCGGGCCGC	4542
rs777099191	snp	C/T	1.68522e-05	0.00290272	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544298	GGCAGGGGGCGCACC[C/T]TGCCAGCGTAGTGGT	4542
rs777116833	snp	A/G	3.35008e-05	0.00409259	intron-variant	MYO1F	GRCh38.p7	19:8536930	GGGAATGAATCTTGG[A/G]TTGGTTGGGGGGGAT	4542
rs777144094	snp	A/G	1.656e-05	0.00287745	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554515	ACAGTCGATAAGCAT[A/G]TTCCGGTACATGTTG	4542
rs777153825	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8530969	GAATCACTTGAACCC[A/G]GGAGGCGGAGGTTGC	4542
rs777191777	snp	C/T	1.66568e-05	0.00288585	missense	MYO1F	GRCh38.p7	19:8522415	TCGTTCACGTTGAAG[C/T]TCAGCTCGTCCACAT	4542
rs777299561	snp	A/G	1.68935e-05	0.00290628	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550178	CACGAGGAAGTCGAA[A/G]AGGCGGGCATAGAGC	4542
rs777308242	snp	G/T	1.65919e-05	0.00288022	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550667	GCTGCTGGATGCTGG[G/T]CGGGATCCCAATAAC	4542
rs777323941	in-del	-/TTC			intron-variant	MYO1F	GRCh38.p7	19:8534608	ACCGTGCCTGGCCTT[-/TTC]TTCTATTTTCATTTT	4542
rs777329862	snp	A/T			intron-variant	MYO1F	GRCh38.p7	19:8528529	CAAGATTCTGACTCA[A/T]CACACACACACAAAA	4542
rs777339567	in-del	-/A			intron-variant	MYO1F	GRCh38.p7	19:8524416	GCTAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	4542
rs777364845	snp	A/G	1.65776e-05	0.00287898	synonymous-codon, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530229	CTTGGTGACCGAATC[A/G]GCGAAGTCCACCCGC	4542
rs777371902	snp	C/T	0.000117882	0.00767639	synonymous-codon	MYO1F	GRCh38.p7	19:8525522	AGGGGCTTGGGACGA[C/T]CTCCGAGGTTTTCCC	4542
rs777379704	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8568219	ACGAGGTCAGGAGAT[C/T]GAGACTATCCTGGCT	4542
rs777399078	in-del	-/CTT	1.65633e-05	0.00287774	cds-indel, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530340	GTTGCGCCTCCGCTC[-/CTT]CTTGTTCAGCAGGAT	4542
rs777482281	in-del	-/CA			intron-variant	MYO1F	GRCh38.p7	19:8556226	GTAGAGATGGGGTTT[-/CA]CCATGTTGGCCAGGC	4542
rs777537386	snp	C/T	1.68343e-05	0.00290118	intron-variant	MYO1F	GRCh38.p7	19:8525456	ACAGACAAGGGAATA[C/T]AGCAAGGGACGCAGC	4542
rs777554421	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8567258	TTTAGTAGAGATGGG[A/G]GTTTCACCATCTTGG	4542
rs777570531	in-del	-/T			intron-variant	MYO1F	GRCh38.p7	19:8538585	TTGCTCCCGGTCTGA[-/T]TTTTTTTTTTTTTTT	4542
rs777571005	snp	C/T	1.66407e-05	0.00288446	missense	MYO1F	GRCh38.p7	19:8522401	GGATCTCAATGACCT[C/T]GTTCACGTTGAAGCT	4542
rs777585517	snp	C/T	1.67967e-05	0.00289794	missense, synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536985	GGCCTCTTGGTCTCG[C/T]TGGGTTTGATGCAGC	4542
rs777667609	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8548940	AATAGCAACTACCTT[A/G]TGGGGCTTTTTCTTT	4542
rs777677983	snp	A/G	3.31581e-05	0.00407161	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555749	CATGTCATCCACGCC[A/G]CTCTGCTTCACGTTG	4542
rs777679368	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8531589	CAAATGACTGGACCT[C/T]CCTGTGCGTCTCTCC	4542
rs777681830	snp	A/G	0.000200958	0.0100219	intron-variant	MYO1F	GRCh38.p7	19:8548341	TGGGTGGGGACAGGA[A/G]GTCAGTGGGCATCGG	4542
rs777703212	snp	C/T	3.31203e-05	0.00406928	synonymous-codon, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8545653	CCCAGCCCTCACCAG[C/T]TTGTTTTCGATGAGG	4542
rs777717265	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8537752	TGATTTTTTTTGAGA[C/T]AGGGTCTCCCTCTGT	4542
rs777761350	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8540431	AATGGTTAATAAGGC[C/T]GGGTGCGGTGGTGCA	4542
rs777771429	snp	C/T	1.72779e-05	0.00293916	intron-variant	MYO1F	GRCh38.p7	19:8530585	AAAGCTGGGCGGGGG[C/T]CGTGGGGGGCAAGGG	4542
rs777775134	snp	C/T	1.65864e-05	0.00287974	intron-variant	MYO1F	GRCh38.p7	19:8550521	ACGCAGTTCACCCAC[C/T]CACAGGCCTCCATCC	4542
rs777799322	snp	C/T	6.60731e-05	0.00574736	intron-variant	MYO1F	GRCh38.p7	19:8553300	GGTGGGGCTGCACTA[C/T]CATGCAGGTGAGGGC	4542
rs777874239	snp	C/T	3.31285e-05	0.00406978	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555687	TCCATGAAGCGCTTC[C/T]GGAGGTTGGCGGCAA	4542
rs777885618	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8558908	GAGATGGGGTCTCAC[G/T]GCTTTGCCCAGGCTG	4542
rs777887982	snp	G/T	2.11522e-05	0.00325202	intron-variant	MYO1F	GRCh38.p7	19:8525605	TGACAGACAGACCAC[G/T]CTCTTTGCCCCGCCC	4542
rs777914288	snp	C/G	1.71962e-05	0.0029322	intron-variant	MYO1F	GRCh38.p7	19:8555828	GGGTCGGGGTGAGCC[C/G]TTGCACGGGGATGCG	4542
rs777978261	snp	C/T	3.31246e-05	0.00406955	intron-variant	MYO1F	GRCh38.p7	19:8551896	GGTGTGCCATGTTCA[C/T]GCATCTGGTGCTTGC	4542
rs778002010	snp	A/C/G	4.95465e-05	0.00497707	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8553190	GTTGCCGAAGGCCTC[A/C/G]AGCAGCGGGTTGGAC	4542
rs778046620	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8559814	AATTAGCTGGGCGTG[C/G]TGGCGCACGCCTGTA	4542
rs778062339	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8522965	AAGGATTGGGCCAGA[C/T]GGAGGGACTCTGCCG	4542
rs778068543	snp	C/G	1.68057e-05	0.00289872	intron-variant	MYO1F	GRCh38.p7	19:8539925	TGCAGGCCCAGCTCC[C/G]CGTTGTACACCCCAG	4542
rs778162186	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8563633	CCTGCCTCAGCCTCC[C/T]TAGTAGCTGGGGTTA	4542
rs778198680	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8552697	AGTTGCATAGATTTT[C/T]TTCCCCCCCAGGCTA	4542
rs778229388	snp	C/T	1.67638e-05	0.0028951	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8526906	TCGGCGGCATCCTCT[C/T]GGAGGATGAAGAAGT	4542
rs778263981	snp	C/T	1.75987e-05	0.00296631	intron-variant	MYO1F	GRCh38.p7	19:8547989	CATGGTCCTTCCACC[C/T]CACCCCCACCCCAGG	4542
rs778285891	snp	A/G	0.00089404	0.0211239	intron-variant	MYO1F	GRCh38.p7	19:8554599	GTCAGGTCTCAGCCC[A/G]GGGCTGGGGGCCAGG	4542
rs778349518	snp	C/T	1.65669e-05	0.00287805	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8548085	TGCTGCAGCTTCTCA[C/T]TGACGAAGTTGATGC	4542
rs778354602	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8524825	GCTCAACGAATGGAA[C/T]GGGAATTTGAGAGAG	4542
rs778366731	snp	C/T	0.000115953	0.00761333	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554679	TAGAGGTCGATCTCA[C/T]GGTCGGTGAAGTAGG	4542
rs778428405	snp	C/T	1.86663e-05	0.00305496	intron-variant	MYO1F	GRCh38.p7	19:8525578	CTGAAAGAAGAGTGT[C/T]AGGGAGTTGAATGAC	4542
rs778441768	snp	G/T			intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8529937	TGTGATGGAACAGAT[G/T]GATCTAGGCTGGGGG	4542
rs778454470	snp	C/T	3.32934e-05	0.0040799	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8527338	AGGACCTGGCTTCAC[C/T]TGAGGGAGACTCCCC	4542
rs778479659	snp	C/T	1.69729e-05	0.0029131	missense	MYO1F	GRCh38.p7	19:8521539	CAGCTCAGATCTTCT[C/T]CACGTAGTTTCCTGG	4542
rs778512373	in-del	-/A			intron-variant	MYO1F	GRCh38.p7	19:8564426	CTGGGATGCACTGAG[-/A]AGTCCCTGGGGTGCG	4542
rs778532982	snp	C/T	1.67787e-05	0.00289639	missense, synonymous-codon, utr-variant-3-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536580	TTCAGGCCCAGGTAT[C/T]CCACCTGGTGCTTGA	4542
rs778562517	snp	A/G	3.31274e-05	0.00406972	intron-variant	MYO1F	GRCh38.p7	19:8554607	TCAGCCCAGGGCTGG[A/G]GGCCAGGAGTCTGGG	4542
rs778653269	snp	C/T	1.65946e-05	0.00288046	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555760	CGCCGCTCTGCTTCA[C/T]GTTGTGGCTCTGCCA	4542
rs778657851	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8553009	GTCTCCCCTTCAGGA[A/G]TAGGTATTTCCTGCT	4542
rs778731414	snp	C/T	1.65721e-05	0.0028785			GRCh38.p7	19:8530426	CCAGGTCCTTGTGCC[C/T]CCACCCCGCGCCGTT	4542
rs778747696	in-del	-/C	1.67517e-05	0.00289406			GRCh38.p7	19:8555795	AAGCGCTCCTTGCTG[-/C]CCTGGGGGGTGAGAG	4542
rs778767239	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8548880	GGTGTGAGCCACTGC[A/G]CCCGGCCTTGCACCT	4542
rs778786394	snp	C/G	3.37206e-05	0.00410599	missense	MYO1F	GRCh38.p7	19:8525526	GCTTGGGACGACCTC[C/G]GAGGTTTTCCCTTGG	4542
rs778915917	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8531380	AAAAGACAGGGTCTC[A/G]CTCCGTCGCCCAGAC	4542
rs778945182	snp	C/T	3.31406e-05	0.00407053	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550632	CAGGTGCAAGATCCC[C/T]GCCACGAGCTGCAGG	4542
rs779006672	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8569828	GTCATGGTCCTGGAG[A/G]GATAGACAGCCCAGG	4542
rs779028359	snp	A/G/T	3.32752e-05	0.00407881	intron-variant	MYO1F	GRCh38.p7	19:8552216	CTGGGGTGCAGGTGG[A/G/T]GGAAGGGTTGGGGAT	4542
rs779032954	snp	C/T	1.65608e-05	0.00287752	intron-variant	MYO1F	GRCh38.p7	19:8545602	ATCTTCCAGACTCAG[C/T]TCAGGGGACCAGTGA	4542
rs779066519	snp	A/G	1.74555e-05	0.00295423	intron-variant	MYO1F	GRCh38.p7	19:8521653	GCTGGCCCTGGAGAA[A/G]GCTCTCATGCCTGGT	4542
rs779096629	snp	C/G	1.65605e-05	0.0028775	intron-variant	MYO1F	GRCh38.p7	19:8548164	CCTCAATGTCCTGGT[C/G]CTGGAAGTTCTTGTG	4542
rs779097714	snp	C/G	1.67584e-05	0.00289464	missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536276	GTTCTTGACAAAGAC[C/G]TTGGTGCTCCCCATC	4542
rs779109686	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8539649	TTTATGTCATGTATA[G/T]TTTACCACAAATTTA	4542
rs779127127	snp	C/T			utr-variant-3-prime, downstream-variant-500B	MYO1F	GRCh38.p7	19:8521083	TGAAAACATCGTCCT[C/T]GTTGGGCACTTAGTA	4542
rs779141648	snp	C/T	1.65734e-05	0.00287862	intron-variant	MYO1F	GRCh38.p7	19:8550542	GCCTCCATCCAGCCC[C/T]CCCTGATACCCACAC	4542
rs779200718	snp	C/T	1.74921e-05	0.00295732	synonymous-codon	MYO1F	GRCh38.p7	19:8522654	CATGCCCTGGTCAGG[C/T]ACGTTGAGGAATTCT	4542
rs779215578	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8533806	CTGTCCCAGCAGACT[A/G]TTATAACATACCTGG	4542
rs779229237	snp	C/G	8.33396e-05	0.00645468	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8553405	CCCATGATATATTTG[C/G]CTGCCACTGTCTTCC	4542
rs779230794	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8530648	CCGGGTTTTCCCTGC[A/G]CTCACCCTACTCACA	4542
rs779255303	snp	A/C/G	3.4661e-05	0.00416287	intron-variant	MYO1F	GRCh38.p7	19:8530590	TGGGCGGGGGTCGTG[A/C/G]GGGGCAAGGGTGAGT	4542
rs779289407	snp	C/G/T	0.000215571	0.0103799	intron-variant	MYO1F	GRCh38.p7	19:8551975	GTGTTTACCTTCCCA[C/G/T]TGTCCACCCCGCTGG	4542
rs779362491	snp	A/T	2.01761e-05	0.00317611	intron-variant	MYO1F	GRCh38.p7	19:8522569	CACAGGGGGTTTGAG[A/T]CACAGCCCCAGACAC	4542
rs779362654	snp	C/T	1.72216e-05	0.00293437	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8527473	GTCAGGATCAAGTCC[C/T]GCTTGATGGGCTGTG	4542
rs779415968	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8550835	TTTCAGTCACTTGCC[A/G]CGTGACCTTGGGTAA	4542
rs779460375	snp	A/G	1.67548e-05	0.00289432	intron-variant	MYO1F	GRCh38.p7	19:8541869	CCATCCCCTTGGGGG[A/G]TTGTAGCCGGAGGTC	4542
rs779481404	snp	A/G	1.65652e-05	0.0028779	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8548090	CAGCTTCTCATTGAC[A/G]AAGTTGATGCAAAAC	4542
rs779513336	snp	C/T	1.65847e-05	0.0028796	intron-variant	MYO1F	GRCh38.p7	19:8551980	TACCTTCCCATTGTC[C/T]ACCCCGCTGGGCTCC	4542
rs779559784	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8564828	CCCAGGCTGGAGTGC[A/G]GTGGTATGATTTCGG	4542
rs779568004	snp	C/T	3.428e-05	0.00413991	intron-variant	MYO1F	GRCh38.p7	19:8521635	AAGCTTGAGGTGCCC[C/T]TAGCTGGCCCTGGAG	4542
rs779605352	snp	A/G	1.65655e-05	0.00287793	intron-variant	MYO1F	GRCh38.p7	19:8548200	CCTGGGCTGCCCCAG[A/G]GAGGACAGGATGTGG	4542
rs779675539	snp	G/T	0.00594475	0.0541944	intron-variant	MYO1F	GRCh38.p7	19:8536658	AGTCCTGGGGGTGGG[G/T]GGGAGGTGCTGGAGG	4542
rs779696505	snp	A/T	1.65669e-05	0.00287805	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554691	TCACGGTCGGTGAAG[A/T]AGGGCATCTGCTTGA	4542
rs779762135	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8563708	GTAGAGATGGGCTTT[C/G]ACTATGTTGGTCAGG	4542
rs779781576	snp	C/G	2.00959e-05	0.00316978	intron-variant	MYO1F	GRCh38.p7	19:8525599	GTTGAATGACAGACA[C/G]ACCACGCTCTTTGCC	4542
rs779788194	in-del	-/A	3.31203e-05	0.00406928	frameshift-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554557	GTAGATGTGCGGGGG[-/A]TTCTCATACTGGGCC	4542
rs779911108	snp	C/T	1.67713e-05	0.00289575	synonymous-codon	MYO1F	GRCh38.p7	19:8521552	CTCCACGTAGTTTCC[C/T]GGGAAAAGGCCCTCC	4542
rs779921382	in-del	-/TTC			intron-variant	MYO1F	GRCh38.p7	19:8533336	CCCAGCCTCAGATTC[-/TTC]TTCTTCTTCTTCTTC	4542
rs779938821	snp	C/G	1.69424e-05	0.00291048	missense	MYO1F	GRCh38.p7	19:8525537	CCTCCGAGGTTTTCC[C/G]TTGGCCATTCCCTTC	4542
rs779943188	snp	C/T	1.72671e-05	0.00293824	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544401	GTGTCTGGTCTGCTC[C/T]CCCGCCCGTGGCGTG	4542
rs779950855	in-del	-/AAAC			intron-variant	MYO1F	GRCh38.p7	19:8528224	AAGACCCTGTCTCAA[-/AAAC]AAACAAACAAAAAAT	4542
rs780004221	in-del	-/CT			intron-variant	MYO1F	GRCh38.p7	19:8525923	TTCCTTGCTGTTGCC[-/CT]CTCTGGTCCAGCCTG	4542
rs780031495	snp	C/G	1.66899e-05	0.00288871	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8536496	GGGTGGAGGGCTCCT[C/G]ACCTCTGCAGGAATT	4542
rs780033132	snp	C/G/T	3.63757e-05	0.0042646	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544444	CACGTCGTCCAAGAC[C/G/T]CTCATGATGCCTGGG	4542
rs780034209	snp	G/T	3.31422e-05	0.00407063	intron-variant	MYO1F	GRCh38.p7	19:8545770	TGGATGTGGGGGCCA[G/T]TGAAAAAGTTGTGGC	4542
rs780036316	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8562371	GGAGTGCACTGGTGC[A/G]ATCATACCTCACTGC	4542
rs780044331	snp	C/G/T	3.30421e-05	0.0040645	intron-variant	MYO1F	GRCh38.p7	19:8553250	CAGAGGCAGGTGGAG[C/G/T]GGGAAGAAGTCAGAC	4542
rs780049697	in-del	-/AGGAT	3.41574e-05	0.0041325	intron-variant	MYO1F	GRCh38.p7	19:8548002	CCCCACCCCCACCCC[-/AGGAT]CCCCCATCCCTGACT	4542
rs780059279	snp	C/T	1.65603e-05	0.00287747	missense, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8545664	CCAGCTTGTTTTCGA[C/T]GAGGTCACAGACGAC	4542
rs780078924	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8574307	TCCCCAATTACCACA[A/G]TCGTCACCTCCGTCC	4542
rs780145005	snp	A/G	1.70301e-05	0.00291801	synonymous-codon, missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8537005	TTTGATGCAGCGGAT[A/G]TAGTGGGGTGTGCAC	4542
rs780174055	snp	C/T	3.31285e-05	0.00406978	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555697	GCTTCCGGAGGTTGG[C/T]GGCAATGGCGTCTTC	4542
rs780234079	snp	A/G	3.32917e-05	0.0040798	synonymous-codon	MYO1F	GRCh38.p7	19:8522408	AATGACCTCGTTCAC[A/G]TTGAAGCTCAGCTCG	4542
rs780236834	snp	A/G	3.36825e-05	0.00410367	missense, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8541988	CGCTGACGTCGTAGG[A/G]GACCTGGAGGGGACA	4542
rs780330235	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8550142	TCCACTCTGCCTTCC[A/G]GCCCCAGCCCCACTC	4542
rs780387141	in-del	-/AG			intron-variant	MYO1F	GRCh38.p7	19:8569327	TTGTGAAAGGCAGTC[-/AG]GGGCTTGAGGTGGGT	4542
rs780397480	snp	C/T	0.000306701	0.0123797	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526642	GGCGCTGGCTGAGGT[C/T]CCCCGCCCCACCCAA	4542
rs780400993	snp	C/G	1.74885e-05	0.00295701	intron-variant	MYO1F	GRCh38.p7	19:8530607	GGGCAAGGGTGAGTC[C/G]TGGTGTCTCCCCAGG	4542
rs780421405	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8549545	TGAGACAGAGTCTCT[C/T]TCTGTTGCCCAGGCT	4542
rs780493471	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8533529	CTGGCTAACTTTTTT[A/G]TATTTTTTTAGTAGA	4542
rs780509524	in-del	-/AGG			utr-variant-3-prime	MYO1F	GRCh38.p7	19:8521336	TGTTGGAGGAAGACC[-/AGG]AGGGCCCAGGGGCGG	4542
rs780576676	snp	C/G/T	5.91679e-05	0.00543884	missense	MYO1F	GRCh38.p7	19:8522739	GTGGACGGAGGGCCC[C/G/T]GGGGAGGCCTGTGGG	4542
rs780585139	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8550752	CTCCAACCTGCCTCC[A/G]GGGGCAGGCTTGAGG	4542
rs780667806	in-del	-/G/GGG	3.46148e-05	0.0041601	intron-variant	MYO1F	GRCh38.p7	19:8530588	CTGGGCGGGGGTCGT[-/G/GGG]GGGGGGCAAGGGTGA	4542
rs780705515	in-del	-/CACACACA			intron-variant	MYO1F	GRCh38.p7	19:8553868	AGACTGAGACTCTGT[-/CACACACA]CACACACACACACAC	4542
rs780727685	in-del	-/ATCTT	1.65828e-05	0.00287943	intron-variant	MYO1F	GRCh38.p7	19:8545785	TGAAAAAGTTGTGGC[-/ATCTT]CACCCTTCCCCCCAT	4542
rs780739771	snp	C/T	1.65608e-05	0.00287752	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8552082	TTTTGCATGACCACG[C/T]GGGACTTCTCCAGCA	4542
rs780806079	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8562550	TTTACTTATTTATTT[C/T]TTTGAGGCAGGGTCT	4542
rs780806680	snp	A/G	4.96989e-05	0.00498467	synonymous-codon, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530270	CCAGGAACTGACGCA[A/G]CTCGGGCCGCTCCTC	4542
rs780819056	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8539470	GTGTGGTGGCGCATG[C/T]TTGTAATCCCAGCTA	4542
rs780824357	snp	C/T	6.62471e-05	0.00575492	intron-variant	MYO1F	GRCh38.p7	19:8548232	CTGGAGGCAGGGGGC[C/T]GTACCTGGAAGATCT	4542
rs780912457	snp	A/G	6.89513e-05	0.00587119	intron-variant	MYO1F	GRCh38.p7	19:8521642	AGGTGCCCCTAGCTG[A/G]CCCTGGAGAAAGCTC	4542
rs780941697	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8529535	CTATGGACTAGGCTG[C/T]CTGGGCCAGGTGAGA	4542
rs780966187	snp	C/G	3.31565e-05	0.0040715	missense, nc-transcript-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8530224	TCGTACTTGGTGACC[C/G]AATCGGCGAAGTCCA	4542
rs780999117	snp	A/G	0.000241109	0.0109771	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8544453	CAAGACGCTCATGAT[A/G]CCTGGGGGGCTCTGC	4542
rs781005834	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8528663	TCAGTGAACAGGTGC[C/T]GGGTAGGTAAGGCAC	4542
rs781008093	snp	C/T	1.66496e-05	0.00288522	intron-variant	MYO1F	GRCh38.p7	19:8555583	CCTCCCTCTGCTCCT[C/T]CACCCTCCTCTCCGT	4542
rs781020934	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8546393	GAGACCGGGTTTTGC[C/T]CTGTTACCCAGGCTG	4542
rs781059040	in-del	-/T			intron-variant	MYO1F	GRCh38.p7	19:8566161	GCTCCAGTCTATGTC[-/T]TTTTTTTTTTTTTTT	4542
rs781073533	snp	A/C/G	0.000167122	0.00913974	missense, synonymous-codon	MYO1F	GRCh38.p7	19:8521573	AAGGCCCTCCTGGCC[A/C/G]TGAAGCCGGCCCTTC	4542
rs781088747	snp	C/T	3.79032e-05	0.00435318	intron-variant, missense, utr-variant-3-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536624	GGTAGGCTGAGTCCC[C/T]TCGGGGTGGGGAGTC	4542
rs781097652	snp	A/G	1.65836e-05	0.0028795	intron-variant	MYO1F	GRCh38.p7	19:8551986	CCCATTGTCCACCCC[A/G]CTGGGCTCCAGGTGG	4542
rs781175033	snp	G/T	0.0282517	0.115446	intron-variant	MYO1F	GRCh38.p7	19:8536674	GGGAGGTGCTGGAGG[G/T]GGGGGACCTGGGGGG	4542
rs781194551	snp	A/C	1.65658e-05	0.00287795	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8550595	GGGCGTAATTCCCGT[A/C]TTCACAGAAACTGAT	4542
rs781219461	snp	G/T	1.70953e-05	0.00292359	intron-variant	MYO1F	GRCh38.p7	19:8555821	GAGAGGGGGGTCGGG[G/T]TGAGCCCTTGCACGG	4542
rs781314430	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8532693	GAGTTCAAGACCAGC[C/G]TGGGCAACATAGAAA	4542
rs781372539	snp	C/T	1.89968e-05	0.00308189	missense	MYO1F	GRCh38.p7	19:8522541	ACGCTGCGCTTCCTC[C/T]GCATGCTGTGGGCAC	4542
rs781374288	snp	C/G/T	8.38714e-05	0.0064753	missense, downstream-variant-500B, nc-transcript-variant	MYO1F	GRCh38.p7	19:8536364	TCGTCCCCACGCCAC[C/G/T]GCGGCCACGTCTCGG	4542
rs781418500	snp	C/T	1.66125e-05	0.00288201	synonymous-codon, nc-transcript-variant	MYO1F	GRCh38.p7	19:8555770	CTTCACGTTGTGGCT[C/T]TGCCAGTGGAAGCGC	4542
rs781464653	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8564814	GTCTCGCTCTGTCAC[A/C]CAGGCTGGAGTGCAG	4542
rs781472471	snp	A/G	1.65603e-05	0.00287747	synonymous-codon, intron-variant, nc-transcript-variant	MYO1F	GRCh38.p7	19:8545689	GACGACCTTGTTGTT[A/G]AAGTACTGGATTGGA	4542
rs781486225	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8554122	GCACCACCGTGTCCG[A/G]CTAATTATTATCTAT	4542
rs781487774	snp	C/T	1.75739e-05	0.00296423	intron-variant	MYO1F	GRCh38.p7	19:8547985	TCCTCATGGTCCTTC[C/T]ACCCCACCCCCACCC	4542
rs781517643	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8566475	CCCGGCCTGGTCTAT[A/G]CTTTTTAAAAAAAAT	4542
rs781530064	snp	A/G	1.7227e-05	0.00293482	missense	MYO1F	GRCh38.p7	19:8522479	TGGGACCATGTGTCC[A/G]AGGCTGGGGCTTGGG	4542
rs781549113	snp	G/T	1.66023e-05	0.00288113	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526765	GACCACCCCGAGATG[G/T]TGCTGGGGTTGGCGG	4542
rs781620626	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8544683	GTGTGTGGGGCTACT[A/G]TGGAAGCTCGCTGAG	4542
rs781673145	snp	G/T	1.65619e-05	0.00287762	intron-variant	MYO1F	GRCh38.p7	19:8554583	GGGCCTGGCAGGGGA[G/T]GTCAGGTCTCAGCCC	4542
rs781677149	snp	C/T	0.000101174	0.00711172	intron-variant	MYO1F	GRCh38.p7	19:8544292	GGTAGGGGCAGGGGG[C/T]GCACCTTGCCAGCGT	4542
rs781696276	snp	C/G/T	0.000125243	0.00791237	intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526429	TGGCCCCGCCCCCTC[C/G/T]GCCCTAGTTCCGCGC	4542
rs781772109	snp	C/G	1.65603e-05	0.00287747	missense, nc-transcript-variant	MYO1F	GRCh38.p7	19:8554487	CATACCTAATGATGA[C/G]ACACTGGTTCTCACA	4542
rs781788537	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8577222	CTCCCCTCACCCCAA[C/T]TTCTGATGGTCATTT	4542
rs781836632	snp	A/G			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578575	GCCTCCAGTTTGGCT[A/G]CTTCCTGGATGACTT	4542
rs781845381	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8576496	TACACAGCAGAGAGC[C/T]GTGGGGTGGGGTCAG	4542
rs781845546	snp	C/T	1.87615e-05	0.00306275	utr-variant-5-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8577354	GGCTCCTGAATGGGT[C/T]GTGATGGAGGTGCAG	4542
rs781850358	snp	A/G			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578353	CATGTTGGCCAGGCC[A/G]GCCTTGAACTCCTGA	4542
rs781851806	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8573837	CCGGGGTGACAGAGC[A/G]AGACTCTGTCTCAGA	4542
rs781858451	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8576458	CACTGACTGAATGAC[A/G]AGAAATGAAAGCTGA	4542
rs781878301	snp	G/T	4.68e-05	0.00483713	utr-variant-5-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8577425	TTCTGCCCGTTCACC[G/T]GACTCCCGGCTTTAG	4542
rs781881287	snp	A/G	1.74385e-05	0.00295278	utr-variant-5-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8577318	TTACCATGGTGGGGG[A/G]CTGGTGTCTGGGCTC	4542
rs781889710	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8575574	AGACAGACCATGGCC[C/T]GATAGCAGTCCATGA	4542
rs781912281	snp	C/T	4.61798e-05	0.00480497	utr-variant-5-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8577423	GCTTCTGCCCGTTCA[C/T]CGGACTCCCGGCTTT	4542
rs781919849	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8576381	CCCTGACTCCACCCT[A/C]GTAAGCTGTACCTGC	4542
rs781935873	snp	A/G	1.72976e-05	0.00294083	intron-variant	MYO1F	GRCh38.p7	19:8577299	GATCCCACCCTTGAA[A/G]GACTTACCATGGTGG	4542
rs781943168	snp	C/G			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578042	TCTAAAAACAAACCA[C/G]AAAAAACAAAAAAAC	4542
rs781950824	snp	C/T			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8577985	AGTGAGCCCTGATTG[C/T]GCCACTGCACTCCAG	4542
rs781956633	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8573383	AGGCAACCAGTGAAC[A/G]TCTTCACTCTCTCTC	4542
rs782014308	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8572176	CTTTTTGGGGAAGAT[A/C]CTCTGGGATGTGGTC	4542
rs782022391	in-del	-/CAAC			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578056	GAAAAAACAAAAAAA[-/CAAC]CCAAAAAAACAACAA	4542
rs782029208	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8575372	GAGCCACCGCACCCG[G/T]CCGGGCATTAGATTG	4542
rs782038697	snp	C/G/T	0.000139664	0.00835557	utr-variant-5-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8577424	CTTCTGCCCGTTCAC[C/G/T]GGACTCCCGGCTTTA	4542
rs782049069	in-del	-/T			intron-variant	MYO1F	GRCh38.p7	19:8570675	CCGCACCCAACCACA[-/T]TTTTTTTTTTTTTAA	4542
rs782052952	snp	C/G	1.73021e-05	0.00294121	intron-variant	MYO1F	GRCh38.p7	19:8577300	ATCCCACCCTTGAAG[C/G]ACTTACCATGGTGGG	4542
rs782063395	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8576416	AATCCTGCAGTGGCC[G/T]CTGTCACAGCCACAT	4542
rs782088291	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8571212	GGAGAGCTAAGCCTC[C/T]GTAGCTGCTTCTGGA	4542
rs782097378	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8573505	ATCAGCCTTCCTTAC[A/G]TTCTCCCACGATCAC	4542
rs782109152	snp	A/C/G	0.000104418	0.00722495	utr-variant-5-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8577316	ACTTACCATGGTGGG[A/C/G]GGCTGGTGTCTGGGC	4542
rs782110445	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8575467	GATAATCTAATGGCG[C/T]CCCCGAGAATCTGAG	4542
rs782126170	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8573330	AAAAAAGAAGAGACA[A/G]TCACTATTATCCTCA	4542
rs782149078	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8574589	TCTTTCTCTCTCTCT[C/T]TCTCTCTCTTTCTTT	4542
rs782156951	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8572577	CCGTGCCCAGTTAGT[A/G]GTCTTAACTGATTCT	4542
rs782164608	snp	C/T	1.73114e-05	0.002942	intron-variant	MYO1F	GRCh38.p7	19:8577282	TCCTCTTTCTTCTTC[C/T]AGATCCCACCCTTGA	4542
rs782180798	snp	A/T			intron-variant	MYO1F	GRCh38.p7	19:8570819	GGCCAAGATGGCTGT[A/T]AATAGTGTGGCCTTG	4542
rs782181820	snp	A/T			intron-variant	MYO1F	GRCh38.p7	19:8575935	CTTGGAAGAATTCCC[A/T]CCCCAACAGTCTCAG	4542
rs782195626	in-del	-/TT			intron-variant	MYO1F	GRCh38.p7	19:8574580	TCTTTCTTTCTTTCT[-/TT]CTCTCTCTCTCTCTC	4542
rs782198199	snp	A/G	6.92321e-05	0.00588313	utr-variant-5-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8577377	AGGTGCAGGTTCAGG[A/G]GGATCTTGGGGGTGG	4542
rs782205119	snp	C/T			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8579181	GATATGGGAAAACCA[C/T]AGGGCAATTGAGGAA	4542
rs782212659	snp	C/G			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8579021	TATGAATGGGTAAGA[C/G]GACCCCACTTTGTTG	4542
rs782232982	snp	C/G	1.90903e-05	0.00308947	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8577464	ACAACAGCCCCTTCT[C/G]ACTTCCTTTGGCGGG	4542
rs782235234	in-del	-/T			intron-variant	MYO1F	GRCh38.p7	19:8575079	TAGATTTTCTTTTTC[-/T]TTTTTTTTTTTTTTT	4542
rs782244664	snp	A/G	7.99808e-05	0.00632329	utr-variant-5-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8577364	TGGGTCGTGATGGAG[A/G]TGCAGGTTCAGGGGG	4542
rs782259421	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8572029	CGCCTGGCCTTTATA[C/T]GTGGGGACCCTTGTC	4542
rs782262560	snp	G/T	2.78913e-05	0.00373428	utr-variant-5-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8577396	TCTTGGGGGTGGCTT[G/T]GGCATGGCCCTGCTT	4542
rs782276731	snp	A/G			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578785	GGAGGTGGCCGAGGC[A/G]GGACCCGACCCTGGG	4542
rs782289810	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8572323	CCCAAGCTGGAGTGT[A/G]GTGGTGCGATCTCAG	4542
rs782292903	snp	A/G	0.000142399	0.00843679	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8577487	TTGGCGGGAGGGGCC[A/G]AGGCCATGGGGGAGG	4542
rs782309393	in-del	-/C/CC			intron-variant	MYO1F	GRCh38.p7	19:8574582	TTTCTTTCTTTCTCT[-/C/CC]CTCTCTCTCTCTCTC	4542
rs782311594	snp	A/G	2.31747e-05	0.00340394	utr-variant-5-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8577379	GTGCAGGTTCAGGGG[A/G]ATCTTGGGGGTGGCT	4542
rs782323052	snp	G/T			utr-variant-5-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8577370	GTGATGGAGGTGCAG[G/T]TTCAGGGGGATCTTG	4542
rs782325456	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8572128	TCTCCACGCAGAAGC[C/T]GGAGCTGGGGAACCC	4542
rs782332719	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8570966	GCTCTGCAGATTCAA[C/T]GAAGCAAAGGTTGTC	4542
rs782347114	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8572069	CTGGGCTCTTTGTCT[C/T]GTCGCTGGAGATTGC	4542
rs782354464	snp	A/G			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8579136	CAGGAGCGTGCACCT[A/G]GCCATGCTAAGCGCT	4542
rs782362043	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8572331	GGAGTGTAGTGGTGC[A/G]ATCTCAGCTCACTGC	4542
rs782365203	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8574904	GGGGTTACAGGCGCG[C/T]ACCACCACGACTGGC	4542
rs782366117	snp	A/G	3.02522e-05	0.00388911	utr-variant-5-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8577402	GGGTGGCTTGGGCAT[A/G]GCCCTGCTTCTGCCC	4542
rs782372147	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8576138	TGTAGCTGGGATTAC[A/G]GGCGTGTGCCACCAC	4542
rs782375956	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8571062	GGCTGGAGGAGGGAG[C/G]TTTTGCAACTCACCC	4542
rs782376775	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8574490	TGGAGCGGGGCATTA[C/G]ATTTTCTTTTCTTTC	4542
rs782396854	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8575363	TACAGGTGTGAGCCA[C/T]CGCACCCGGCCGGGC	4542
rs782411831	snp	C/T			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8579186	GGGAAAACCATAGGG[C/T]AATTGAGGAAGTTCG	4542
rs782412151	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8573241	GCATGAACCTAGGAG[G/T]TGGGGCTTGCAGTGA	4542
rs782431627	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8572737	GTCTGTCTCTGTTGC[C/T]CAGGCTGGAGTGCAG	4542
rs782445361	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8576563	CGATACTGCTAGGAA[C/T]AGCGCCATGATCACG	4542
rs782449356	snp	C/G	1.74821e-05	0.00295647	utr-variant-5-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8577322	CATGGTGGGGGGCTG[C/G]TGTCTGGGCTCCTGG	4542
rs782479857	snp	G/T	3.81396e-05	0.00436673	utr-variant-5-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8577355	GCTCCTGAATGGGTC[G/T]TGATGGAGGTGCAGG	4542
rs782518314	snp	C/T	4.24556e-05	0.00460717	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8577476	TCTCACTTCCTTTGG[C/T]GGGAGGGGCCGAGGC	4542
rs782530323	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8572641	CTGTCCATCCTCATG[A/G]CCACTGATTCTGGAC	4542
rs782551717	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8574593	TCTCTCTCTCTCTCT[C/T]TCTCTTTCTTTCTTT	4542
rs782552397	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8573044	CCAGGTGTGGTGGCT[C/T]ACGCCTATAATCCCA	4542
rs782566603	snp	C/G	0.000274624	0.0117148	utr-variant-5-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8577369	CGTGATGGAGGTGCA[C/G]GTTCAGGGGGATCTT	4542
rs782579949	snp	C/T	0.000105513	0.0072626	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8577459	CTCTTACAACAGCCC[C/T]TTCTCACTTCCTTTG	4542
rs782596546	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8570642	AAAGTGCTGGAATGA[C/T]GGGCACTGGGATGAG	4542
rs782607423	in-del	-/T			intron-variant	MYO1F	GRCh38.p7	19:8574580	TTCTTTCTTTCTTTC[-/T]CTCTCTCTCTCTCTC	4542
rs782618278	snp	A/T	7.0373e-05	0.0059314	intron-variant	MYO1F	GRCh38.p7	19:8577263	TCCACCTGGCTGGTG[A/T]CCCTCCTCTTTCTTC	4542
rs782623120	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8575854	AAGTAGCAAATCACT[G/T]CCTGTGTTCTTTTGA	4542
rs782624405	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8572092	GAGATTGCTGACAGT[C/T]GGTGGCTACCGTCTC	4542
rs782633508	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8573046	AGGTGTGGTGGCTCA[C/T]GCCTATAATCCCAGC	4542
rs782633913	in-del	-/A			intron-variant	MYO1F	GRCh38.p7	19:8577112	CCTGGCATCCCCACC[-/A]CCTACAGATGGGAGC	4542
rs782636325	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8575686	CCACTCCTCCAGGAA[A/G]ATTTCAGCATCCCCA	4542
rs782657883	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8574497	GGGCATTAGATTTTC[G/T]TTTCTTTCTTTTCCT	4542
rs782660784	snp	A/G	0.000115148	0.00758687	utr-variant-5-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8577375	GGAGGTGCAGGTTCA[A/G]GGGGATCTTGGGGGT	4542
rs782664666	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8570997	CAGTGTAAATGCTAG[C/T]GTTCCTCACTGTCCC	4542
rs782674391	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8570130	CAGGCTGGAGTGCAG[C/T]GGCATGATCTAGGCT	4542
rs782691183	snp	C/T	0.000126048	0.00793776	utr-variant-5-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8577343	GGGCTCCTGGAGGCT[C/T]CTGAATGGGTCGTGA	4542
rs782717708	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8576577	ATAGCGCCATGATCA[C/T]GACAGTCTCCCCGTT	4542
rs782730930	snp	A/G	1.73549e-05	0.0029457	utr-variant-5-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8577311	GAAGGACTTACCATG[A/G]TGGGGGGCTGGTGTC	4542
rs782736250	snp	A/T			intron-variant	MYO1F	GRCh38.p7	19:8576482	AAGCTGAAGTGGTCT[A/T]CACAGCAGAGAGCTG	4542
rs782736750	snp	A/C			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578428	ACAGGCATAAGCCAC[A/C]ACGCCTGGCCCAACC	4542
rs782741929	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8572531	CCTCGGCCTCCTAAA[G/T]TGCTGGGATTACAGG	4542
rs782779956	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8575468	ATAATCTAATGGCGC[A/C]CCCGAGAATCTGAGA	4542
rs782798490	in-del	-/G	0.000457352	0.0151151	upstream-variant-2KB	MYO1F	GRCh38.p7	19:8577495	AGGGGCCGAGGCCAT[-/G]GGGGAGGGAAGCTGG	4542
rs782805372	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8573750	AGCTACTTGGGAGGC[C/T]GAGGCACGAGAATTG	4542
rs782808370	snp	A/G	0.000115214	0.00758905	utr-variant-5-prime, nc-transcript-variant	MYO1F	GRCh38.p7	19:8577433	GTTCACCGGACTCCC[A/G]GCTTTAGTTCCTCTT	4542
rs782809936	snp	A/T			upstream-variant-2KB	MYO1F	GRCh38.p7	19:8578215	GCAATCTCAGCTTAC[A/T]TTAATCTCCGCCTCC	4542
rs782820958	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8572585	AGTTAGTGGTCTTAA[C/T]TGATTCTTTCTCCTA	4542
rs796144073	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8534175	CAGAGCGAGACTCTG[C/T]CTAAAAAAAAAAAAA	4542
rs796151880	multinucleotide-polymorphism	CGT/TGC			intron-variant	MYO1F	GRCh38.p7	19:8568283	AAAAATTAGCCAGGT[CGT/TGC]GTGGCGGGCGCCCGT	4542
rs796174742	snp	C/T			utr-variant-3-prime, downstream-variant-500B	MYO1F	GRCh38.p7	19:8520790	GGCTTTTTTTTTTTT[C/T]TTTTTTAAATTTTTA	4542
rs796411164	snp	C/G			intron-variant	MYO1F	GRCh38.p7	19:8548624	TTTTTTTTTTGAGAC[C/G]GAGTCTCACTCTGTC	4542
rs796549221	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8522109	CTCACTGCAAGCTCC[A/G]CCTCCCGGGTTCATG	4542
rs796597810	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8530852	TGAGACGAGCCTGAC[C/T]GACATAGTGAAACCC	4542
rs796606712	in-del	-/TC			intron-variant, downstream-variant-500B	MYO1F	GRCh38.p7	19:8526350	CACAAAACTCAAAAG[-/TC]TCTCTCTCTCTCTCT	4542
rs796624086	in-del	CCC/G			intron-variant	MYO1F	GRCh38.p7	19:8548333	GCGGTGTGGGTGGGG[CCC/G]CAGGAAGTCAGTGGG	4542
rs796625876	snp	A/T			intron-variant	MYO1F	GRCh38.p7	19:8532072	GCAGTGAGCGGAGAT[A/T]GCGCCACTGCACTCC	4542
rs796651480	in-del	-/T			intron-variant	MYO1F	GRCh38.p7	19:8569921	TCAAGGTGCCTGTTA[-/T]TTTTTTTTGGACAGA	4542
rs796651965	snp	A/T			intron-variant	MYO1F	GRCh38.p7	19:8538604	TTTTTTTTTTTTTTT[A/T]AAGAGACAGGGTCTC	4542
rs796656959	in-del	-/AA			intron-variant	MYO1F	GRCh38.p7	19:8556495	AAAAAAGAAAGAAAG[-/AA]AGAAAGAAAGAGAAA	4542
rs796728446	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8534260	AAGCTAATTTAATTT[A/C]TTGATTACTTTTTAA	4542
rs796755709	multinucleotide-polymorphism	CGA/TGG			intron-variant	MYO1F	GRCh38.p7	19:8546747	CAATGGCACAATCTC[CGA/TGG]TCACTACAAGCTCTG	4542
rs796825874	snp	A/G			intron-variant	MYO1F	GRCh38.p7	19:8564250	GCCAGGCGTGGTGTC[A/G]GGCGCCTGTAATCCC	4542
rs796835817	snp	G/T			intron-variant	MYO1F	GRCh38.p7	19:8542516	GCTGCTACCAAAGGT[G/T]AGGGCCCTCTGTAGT	4542
rs796862177	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8532911	AAAAAAATACACACA[C/T]ACACACACACACACA	4542
rs796974823	snp	A/C			intron-variant	MYO1F	GRCh38.p7	19:8556914	AAAAAAAAAAAAGGA[A/C]GCCAATCTGAAAAGG	4542
rs796980106	in-del	-/TT			intron-variant	MYO1F	GRCh38.p7	19:8541426	GTGTGTGTGTGTGTG[-/TT]TTTTTTTTTTTTTTT	4542
rs797011481	snp	C/T			intron-variant	MYO1F	GRCh38.p7	19:8553019	CAGGAGTAGGTATTT[C/T]CTGCTGGGTTTTCAA	4542

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